16130 Closed Entry-Level Biotechnology & Life Science Job Postings
This list includes jobs asking for Associates, Bachelors or Masters degrees and is available in three formats: chronological, alphabetical and geographical. We also keep records of all the old jobs we have posted that are no longer open: Entry-level History
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| Job Information | Description | Date Added | |
| 1 | BioPharmGuy Anywhere, US Contract Data Work some college Exp: 0 yrs |
We are looking for someone with expertise in classifying diseases/conditions by medical specialty to do drug pipeline confirmation tasks. Contract work on a task basis. Must be able to accept payment by PayPal or Venmo. Also must be able to function in the world without using ChatGPT, because if we thought AI could do the task well, you would not be reading this job posting. Please send a message through the contact form if interested. | 04/11/2026 |
| 2 | SHL Medical Deerfield Beach, FL Process Engineer 1 B.S. in Biomedical Engineering/Mechanical Engineering or any relevant branch of study Exp: 0-2 years |
Process Engineers are responsible for supporting the implementation of new process systems into manufacturing production while ensuring that all activities are completed and documented by SHL Pharma Quality System requirements. Serving as the voice of operations between the development site and manufacturing site, the Process Engineer will be responsible for supporting the design, development, testing, and evaluation of assembly, labeling, packaging, and serialization operations. | 12/16/2025 |
| 3 | SHL Medical North Charleston, SC Operations Quality Support Bachelor’s degree Exp: 1+ years |
The Quality Support position is responsible for assisting in operation related quality documentation and tasks including but not limited to open/write up NCMRs and/or ABNs with known root cause and has standard way of revolving. This position will also be responsible for reworking activities that are approved by SHL customers but are not part of daily operation of molding and/or assembly. | 12/16/2025 |
| 4 | SK Life Science Paramus, NJ Analyst, MS&T Master’s degree Exp: 1-2 years |
Manage Contract Manufacturing Organization (CMO) in the following areas: commercial product manufacturing (Drug Substance, Drug Product & Packaging), and testing laboratories (Quality Control for stability, In-Process & Release testing). Primarily responsible for the following, but not limited to; strategy establishment and implementation of New product(s) launch, tech transfer, method/process/packaging validation, etc. Manage CPM project financial tracking. Ensure an uninterrupted supply of commercial product(s) to the marketplace. | 12/16/2025 |
| 5 | SMC Ltd Devens, MA Quality Engineer Bachelor's Degree Exp: 1-3 years |
Responsible for all areas of Quality Engineering and working directly with the engineering, tooling and manufacturing functions to ensure adequate systems and inspection methods and tools are used throughout the plants for molding or assembling products. Understanding customer requirements and implementing required documentation, action plans, purchasing equipment or tools necessary to perform tasks. Ensure proper controls, operator instructions and quality tools used to verify customer’s products meet specifications at all phases within our process. | 12/16/2025 |
| 6 | SMC Ltd Somerset, WI Operations Engineer BS in an applicable Engineering discipline Exp: 0-3 years |
Support Operations with optimal, cost-effective manufacturing processes and methods in accordance with product specification and quality standards. Manage projects from concept through successful completion that meet and exceed the customers’ requirements while matching SMC’s business needs. | 12/16/2025 |
| 7 | Smithers Darien, IL Microbiologist Master’s degree in Microbiology or related field Exp: 6 months - 3 years |
The Associate Microbiologist will conduct microbiological analysis of cannabis flower, concentrates and infused products as required by state cannabis regulatory body regulations within an ISO 17025 accredited laboratory. The Associate Microbiologist will be responsible for coordinating scheduling with the Laboratory Manager and conducting sample analysis. As time allows, the Associate Microbiologist will also be cross-trained to conduct sample onboarding, preparation, and extraction for subsequent chemical analyses. | 12/16/2025 |
| 8 | Sovereign Pharmaceuticals Fort Worth, TX QC Chemist I BA/BS Chem Exp: 0 years |
The primary function of a QC Chemist is to perform qualitative and quantitative chemical and physical analysis in support of raw materials, in-process samples, components, and finished drug products testing. | 12/16/2025 |
| 9 | Spear Bio Woburn, MA Research Associate/Associate Scientist, Assay Development Master's degree in Biology, Biochemistry, Biophysics, Biomedical Engineering or a related discipline Exp: 1-3 years |
We are seeking a highly motivated and experienced Research Associate/Associate Scientist to join our growing Assay Development team, with hands-on experience running ultrasensitive immunoassays and the desire to be at the forefront of innovative research. This individual will play a pivotal role in advancing Spear Bio’s new range of ultrasensitive immunoassays and assay biomarker programs. | 12/16/2025 |
| 10 | Spear Bio Woburn, MA Senior Associate Scientist/Scientist, Assay Development MS in Biology, Biochemistry, Biomedical Engineering or a related discipline Exp: 1+ years |
We are seeking a highly motivated and experienced Senior Associate Scientist/Scientist to join our custom Assay Development team, who has hands-on experience developing and validating custom ultrasensitive immunoassays for clients. The ideal candidate will support the full lifecycle of assay development, from initial concept and research to validation and assay transfer. This individual will play a pivotal role in advancing Spear Bio’s new range of custom ultrasensitive immunoassays and assay biomarker programs. This role is based onsite in our lab in Woburn, MA 5 days/week. | 12/16/2025 |
| 11 | Spectrum Vascular Bridgewater, NJ Regulatory Affairs Specialist Bachelor’s degree in a scientific area Exp: 1-3 years |
The Regulatory Affairs (RA) Specialist is responsible for supporting global regulatory submissions and compliance activities to ensure medical device products meet applicable regulatory requirements throughout their lifecycle. This role collaborates cross-functionally with Quality, Engineering, Clinical, and Manufacturing teams to prepare, submit, and maintain regulatory filings with agencies such as the U.S. FDA, European Notified Bodies, and other international authorities. | 12/16/2025 |
| 12 | SRI Palo Alto, CA Mechanical Engineer Bachelors in Mechanical Engineering or a related field Exp: 1+ years |
The Bright Ceramics Technology group (BCT) is focused on developing, applying, and commercializing a unique technology platform based upon advanced materials. They develop and manufacture cutting-edge components and systems. BCT is currently searching for new grad Mechanical Engineers to join their team. The ideal candidates will be able to perform basic engineering analysis, complete detailed specifications, and be able to build and troubleshoot systems with minimal supervision. Working with interdisciplinary teams, the ME will apply their knowledge of mechanical design and materials properties to invent, fabricate, and test complex components and systems that are benchmarks of elegant and effective design. Successful applicants will be proficient in mechanical design and analysis, prototyping, a wide range of manufacturing processes, electro-mechanical systems, 3D CAD, and system fabrication. | 12/16/2025 |
| 13 | STERIS Brooklyn Park, MN Quality Analyst Bachelor’s degree in Scientific or related technical field Exp: 1 year |
The Quality Analyst in our Brooklyn Park, Minnesota location is responsible for assisting in administration of the quality management system at a site to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. In this role the Quality Analyst will lead complaint/CAPA investigations, supplier quality improvement initiatives, continuous improvement initiatives and countermeasures with the use of statistical techniques and other accepted quality principles. You will execute activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 12/16/2025 |
| 14 | STERIS Spartanburg, SC Quality Analyst Bachelor’s degree (Scientific or related technical field) Exp: 1 year |
The Quality Analyst in the STERIS Applied Sterilization Technologies (AST) Spartanburg, South Carolina facility is responsible for assisting in administration of the quality management system at a site to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. The Quality Analyst leads complaint/CAPA investigations, supplier quality improvement initiatives, continuous improvement initiatives and countermeasures with the use of statistical techniques and other accepted quality principles. The Quality Analyst executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. The Analyst also supports production and quality operations by coordinating and performing problem-solving investigations, pre-reviews and final acceptance/run release of processing runs that contain non-conformances. | 12/16/2025 |
| 15 | STERIS Libertyville, IL Quality Analyst Bachelor’s degree in Scientific or related technical field Exp: 1 year |
The Quality Analyst in our Libertyville, IL location is responsible for assisting in administration of the quality management system at a site to assure adherence to ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, and/or ISO 11137 and other applicable regulatory standards. In this role the Quality Analyst will lead complaint/CAPA investigations, supplier quality improvement initiatives, continuous improvement initiatives and countermeasures with the use of statistical techniques and other accepted quality principles. You will execute activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 12/16/2025 |
| 16 | STERIS Cleveland, OH Validation Engineer I Bachelor’s Degree in Mechanical Engineering, Bio Medical, Bio engineering, Chemical or Engineering General Exp: 1-5 years |
At STERIS, we’re dedicated to creating a healthier and safer world by providing innovative healthcare and life science solutions globally. We’re currently seeking a talented Validation Engineer to join our team. If you’re passionate about validation, enjoy travel, and want to be a subject matter expert, this role might be perfect for you! As a Validation Engineer at STERIS, you’ll play a crucial role in ensuring the reliability and compliance of our products in cGMP-regulated markets. You’ll author and execute validation protocols for STERIS equipment while also providing consultative support and training to our Service Representatives and Customers. Your expertise will contribute to the development and delivery of validation-related services across pharmaceutical, biotechnology, medical device, and laboratory research sectors. If you’re ready to contribute to our mission and thrive in a dynamic environment, we’d love to hear from you! | 12/16/2025 |
| 17 | Stratus Therapeutics Watertown, MA Manufacturing Associate I BA/BS degree in a science related discipline Exp: 0-2 years |
Stratus Therapeutics is seeking a motivated Manufacturing Associate/Sr. Manufacturing Associate to support routine GMP Manufacturing operations. This includes day-to-day operational tasks including but not limited to Cell Culture in a clean room environment, GMP Materials Logistics, and Environmental Monitoring within Stratus GMP manufacturing space. This is an on-site role, primarily in Watertown, MA with occasional work in Cambridge MA. Some travel between sites is required. | 12/16/2025 |
| 18 | Stryker Franklin, TN Quality Control Analyst I Master’s degree in biology, biochemistry, microbiology, or chemistry Exp: 1-2 years |
The QC Analyst I will perform routine and complex analytical testing to support lot release, stability, and method development, while accurately documenting results and ensuring all work meets cGMP/cGLP standards. | 12/16/2025 |
| 19 | Stryker Salt Laker City, UT Quality Engineer Bachelor of Science in Engineering or related discipline Exp: 0+ years |
Stryker is hiring a Quality Engineer to support our Neurovascular division in Salt Lake City, Utah. This is an onsite role requiring in-office presence 5 days per week. As Quality Engineer, you will champion quality and lean methodologies, drive process improvements, and ensure compliance to deliver superior products to patients and customers. | 12/16/2025 |
| 20 | Supernus Pharmaceuticals Rockville, MD Chemist Analytical Sciences PA Bachelor’s degree in life sciences (Chemistry degree) Exp: 0+ years |
The Chemist Analytical Sciences PA will provide analytical support for pharmaceutical solid dosage forms primarily by using dissolution testing, spectroscopy, HPLC, wet chemistry, including maintaining proper documentation. | 12/16/2025 |
| 21 | Shifamed Los Gatos, CA Manufacturing Engineer Bachelor’s in Mechanical, Biomedical Engineering or equivalent Exp: 0-3 years |
The Manufacturing Engineer contributes to medical device product design, development, manufacturing, and testing in accordance with the company’s Quality System. Helps generate design outputs where required through interface with cross-functional team members. | 12/16/2025 |
| 22 | Syner-G Worcester, MA Project Engineer Bachelor’s or advanced degree (e.g., B.S., M.S.) in Mechanical, Electrical, Civil Engineering, Facilities Engineering, or related discipline Exp: 1-5 years |
The Project Engineer is responsible for the strategic oversight and hands-on management of building systems, infrastructure projects, and utility operations across the organization. This role ensures optimal performance, safety, and compliance of all facilities-related functions, including HVAC, electrical, plumbing, and environmental systems. The Engineer will lead cross-functional initiatives, manage capital projects, and serve as a technical expert in building operations, cleanroom design, and sustainability efforts. The ideal candidate operates independently and proactively, driving continuous improvement and operational excellence. | 12/16/2025 |
| 23 | Syner-G Boston, MA Project Engineer Bachelor’s or advanced degree (e.g., B.S., M.S.) in Mechanical, Electrical, Civil Engineering, Facilities Engineering, or related discipline Exp: 1-5 years |
The Project Engineer is responsible for the strategic oversight and hands-on management of building systems, infrastructure projects, and utility operations across the organization. This role ensures optimal performance, safety, and compliance of all facilities-related functions, including HVAC, electrical, plumbing, and environmental systems. The Engineer will lead cross-functional initiatives, manage capital projects, and serve as a technical expert in building operations, cleanroom design, and sustainability efforts. The ideal candidate operates independently and proactively, driving continuous improvement and operational excellence. | 12/16/2025 |
| 24 | Synfini Menlo Park, CA Chemistry Technician Bachelor’s degree in Chemistry, Chemical Technology, or a related field Exp: 1-2 years |
We are seeking a detail-oriented and motivated Lab Operations Technician to join our chemistry laboratory team. In this role, you will support the operation of customer-facing automated synthesis workstations. You will be responsible for preparing stock solutions, maintaining the instruments, running quality control procedures and maintaining the chemical inventory. | 12/16/2025 |
| 25 | Takara Bio San Jose, CA QA Associate I BA/BS degree in a scientific discipline or engineering Exp: 0-2 years |
The QA Associate I role is responsible for providing general support to the Quality department. This role helps to maintain the quality management system under close supervision and guidance. QA Associate I is responsible for carrying out general quality functions or activities, as assigned. The QA Associate I receives guidance on workload prioritization from the team lead or management but is ultimately responsible for organizing and executing their projects and daily standard workload in a manner which meets the schedules of the operational teams whom they support. The QA Associate I is an on-site role located in San Jose, CA. | 12/16/2025 |
| 26 | Tandem Diabetes Care Barnes, CA Quality Engineer I Bachelor’s degree in Engineering, preferably Mechanical Engineering or the equivalent Exp: 6 months |
Responsible for providing quality guidance and support for product launch, sustaining engineering, production and quality system activities to assure conformance to established specifications. Facilitates the optimization and continuous improvement of internal operations to meet department, business unit and company objectives. | 12/16/2025 |
| 27 | Tandem Diabetes Care High Bluff, CA Systems Test Technician Bachelor’s degree Exp: 1 year |
Supports engineering activities such as design and execution of system level testing. Includes development of protocols, test methods, and test equipment required to verify system performance. | 12/16/2025 |
| 28 | TCG GreenChem Ewing, NJ Technician I / II (Kilo Lab) Bachelor’s degree in science or a related discipline Exp: 1-2 years |
The basic purpose is to conduct technical activities according to protocols. Receives daily tasking assignments, under moderate supervision. Functions as a member of work team by assisting others and promoting a team-oriented work environment. Performs all work in conformance with applicable regulations. Performs all work in a safe manner. Works within the laboratory or processing environment. | 12/16/2025 |
| 29 | TD2 Scottsdale, AZ Research Associate - In Vitro Pharmacology Bachelor’s degree Exp: 1-2 years |
The TD2 Research Associate - In Vitro Pharmacology is involved in many aspects of laboratory operations primarily tissue culture activities, various cell-based assays, and molecular biology experiments. This position requires great attention to detail while working in a deadline-driven environment. | 12/16/2025 |
| 30 | Tempus Research Triangle Park, NC Quality Control Reagents I - IV BS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work within a cutting-edge genomics workflow to provide quality control support in a high-volume clinical molecular laboratory. Test and document new lots of reagents for clinical lab team processing and label reagents approved for use. Maintain reagent qualification records and manage quality control of reagent inventory. Document all results and findings in order to satisfy CLIA/CAP/NYS-DOH/ISO compliance. Collect and help analyze metrics. Investigate reagent related issues and help facilitate and implement corrective and preventative actions. Interact with lab management and personnel to provide training, troubleshoot issues, and prioritize QC tasks. Report significant findings/deviations and system deficiencies to lab management, as appropriate. Update SOPs and records within the document control system, including creation/ revision/ review of internal SOPs and other quality documentation. Complete Performance Qualifications (PQs) and support the Lab QC team with equipment and documentation tasks as needed. Monitor and respond to laboratory temperature excursions. | 12/16/2025 |
| 31 | Tempus Chicago, IL Molecular Technologist I/II (High Complexity) BS/MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1-2+ years |
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time. | 12/16/2025 |
| 32 | Tempus Chicago, IL Molecular Technologist I (Extractions) BS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 0-1+ years |
Work with a cutting-edge genomics workflow to provide high-quality data with rapid turnaround times in a clinical laboratory. Perform routine testing, quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform nucleic acid extraction and DNA/RNA quantification and qualification using robotics and automated liquid handlers. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Obtain 12 continuing education hours in the field of oncology or molecular biology. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 12/16/2025 |
| 33 | Terray Therapeutics Monrovia, CA Senior Research Associate, Protein Biophysics MSc degree Exp: 1+ years |
Terray Therapeutics is seeking a highly independent, motivated, and creative protein biochemist to join our preclinical team. An ideal candidate will have full responsibility of protein quality control workflows and be a pivotal member in collaboration between our screening and assay development teams. Successful candidates will be expected to be familiar with basic physical properties of targets of interest (based on literature and experimental sources) and play a key role in protein engineering, initial assay development and optimization. This position offers a unique opportunity to have an independent role and be a pivotal part of a multidisciplinary team in the frontiers of drug discovery. | 12/16/2025 |
| 34 | The Ritedose Corporation Columbia, SC Process Development Engineer Bachelor degree in Chemical or Mechanical Engineering Exp: 1-3 years |
Process Development Engineer is responsible for designing and implementing processes for development products. The Engineer will design and implement appropriate change requests, packing studies, batch records, forms, procedures, work instructions, risk assessments, etc. as needed to achieve the development and production goals of the organization. The Engineer’s responsibility will include Formulation, Filling, Bulk and Finished Packaging development as assigned by management. | 12/16/2025 |
| 35 | Thermo Fisher Scientific Highland Heights, KY Laboratory Supervisor, - Hematology, PBMC (2nd Shift) Bachelor's degree Exp: 1+ years |
As a Laboratory Supervisor you will play a crucial role in ensuring the smooth and efficient operation of our laboratory unit. This position involves supervising daily work activities, maintaining high standards of scientific and administrative operations, and ensuring compliance with all safety and quality protocols. Key responsibilities include operating, maintaining, and repairing clinical laboratory equipment, performing routine preventive maintenance, calibrations, and safety checks, and overseeing weekly and monthly Quality Control processes. Additionally, the supervisor will manage the Quality Control database and assist in setting up and validating new assays as directed by the manager. | 12/16/2025 |
| 36 | Thermo Fisher Scientific Worcester, MA Associate Scientist – Buffer / Media Preparation Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar Exp: 0-2 years |
Independently performs routine and non-routine testing. Performs laboratory scale activities to support PDS&T, Pilot Lab Process Development. These activities range from media/buffer preparation to direct project support under the supervision of relevant subject matter experts. Successfully manages time to execute activities within project demands. Manages consumable and raw material forecasting and stocking in a high-volume laboratory setting. Recognizes and resolves moderate challenges in the lab space with their routine workflows. Actively enhances and recommends new workflows based on the evolving needs of the Pilot Lab and PDS&T teams. | 12/16/2025 |
| 37 | Thermo Fisher Scientific Greenville, NC QC Scientist I (12 hour Night Shift) Bachelor’s degree in a biology/ related field Exp: 1+ years |
A successful person will perform Environmental Monitoring tasks in support of Steriles production within classified areas. The individual is encouraged to follow the 4i Values that are held in high regards by the company when completing their work. The four values are integrity, innovation, intensity, and involvement. The job function includes aseptic technique which requires the individual to gain knowledge of aseptic gowning as well as working in cleanrooms in order to monitor the area while sterile products are filled and manufactured. Typical shift hours are 6pm-6am on a 2-2-3 rotating schedule. | 12/16/2025 |
| 38 | Thermo Fisher Scientific Cincinnati, OH Scientist II, Manufacturing Sciences Bachelor's degree in chemical engineering (or other engineering field), chemistry, pharmacy, or other related science or technical field Exp: 1-3 years |
As a Manufacturing Scientist II, you will lead and/or implement activities for the development of new and established manufacturing processes of solids, liquids, and semi-solid dosage forms. Project management skills will be applied to implement the scaling up manufacturing processes, supporting new product validations and post approval qualifications activities. This will require the writing, approval, and routing documents within a manufacturing setting. You will be the primary technical representative on client projects and will work closely work with internal and external project teams of analytical, quality, and project management representatives. Supporting process development and commercial activities will be required. Leads technical/scientific project activities and discussions to lead strategies and technical solutions that meet client needs and expectations. | 12/16/2025 |
| 39 | Thermo Fisher Scientific Middleton, WI EHS Manager Bachelor's or Master's degree in occupational safety, environmental health, life science or natural science or equivalent Exp: 1+ years |
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. | 12/16/2025 |
| 40 | Thermo Fisher Scientific Middleton, WI Lab Supervisor (GMP, Biopharmaceuticals) Bachelor's degree Exp: 1+ years |
As a Lab Supervisor you will coordinate staffing and resources, support day-to-day workflows, and assist in preparation and implementation of company policies, quality systems and training programs. This role ensures that projects are completed in a timely manner so that company revenues are met, and clients are satisfied with the quality and turnaround of work being performed. The Lab Supervisor also ensures that staff continue to be developed to keep pace with department goals and growth. | 12/16/2025 |
| 41 | Thermo Fisher Scientific Cincinnati, OH Equipment Engineer II Bachelor’s Degree in Engineering (industrial, manufacturing, chemical, or mechanical engineering) Exp: 1+ years |
Carries out management of engineering projects including estimating costs, sourcing, identifying, specifying, purchasing and installing equipment, crafting/modifying existing or new facilities, and the commissioning and qualification of equipment, utilities and facilities to meet site/company requirements. | 12/16/2025 |
| 42 | Pfizer Sanford, NC Engineering Validation Associate Bachelor's degree Exp: 0+ years |
Evaluate, review, and approve validation master plans, protocols, and reports, ensuring compliance with regulatory requirements and company policies. Troubleshoot validation problems for equipment and performance processes, conducting statistical analysis of testing results to address process anomalies. Write, review, and approve validation process documents and technical reports related to equipment, products, and processes. Contribute to project tasks and milestones, organizing work to meet deadlines and applying basic team effectiveness skills within the immediate Work Team. Make decisions within limited options to resolve basic problems, working under the supervisor's direction and seeking guidance from colleagues. Ensure work is regularly reviewed for technical judgment, completeness, and accuracy, exercising judgment with reliance on the supervisor. Determine the process capability of new equipment through the execution of approved protocols, incorporating defined parameters into operating procedures and batch records. Assist with the development of validation protocols, manage regulatory queries and responses, and participate in deviation investigations to identify root causes and define corrective and preventative actions. Adhere to all company and Good Manufacturing Practices (cGMP) procedures, safety regulations, and participate in the development of validation programs to stay current with cGMPs and industry standards. Work effectively as a member of the Engineering Validation team, collaborating with Business Area Training Leads, Coordinators, and SMEs to support cGMP and site training initiatives, reporting to the Validation Section Manager and summarizing data into concise reports for review and approval. | 12/08/2025 |
| 43 | Pfizer Rocky Mount, NC Tech Services - Senior Associate Engineer Master's degree Exp: 0+ years |
As a Senior Tech Ops Engineer, you will play a crucial role in improving patients' lives while working at Pfizer. Your contributions will directly impact the development and delivery of innovative solutions that enhance the quality of life for patients worldwide. Join us in our mission to bring breakthroughs that change patients' lives. The Sr Tech Ops Engineer provides strategic direction and technical expertise for site Commissioning and Qualification (C&Q) activities for equipment, utilities and facilities. To include execution of C&Q work for utilities, facilities and global applications as well as maintenance and execution of periodic performance qualification schedule and reviews. This role serves as a Center of Excellence, driving alignment with global and industry engineering standards. The engineer supports site critical programs related to C&Q while also supporting capital project execution and site-wide technical initiatives. The position plays a key role in shaping the site’s technology roadmap, ensuring operational excellence, and fostering a self-sustaining technical work structure for the Focus Factory Manufacturing Technology teams. | 12/08/2025 |
| 44 | Pfizer Rocky Mount, NC Sr. Associate, Learning & Development (L&D II) Master's degree Exp: 0+ years |
In this role, you will act as a change agent, facilitate job shadowing and apprenticeship programs, manage knowledge management, and conduct operator trainer qualifications. You will design and update curricula plans, manage strategic change initiatives, assist in developing departmental strategy by designing training and L&D programs, and participate in continuous improvement projects. You will provide metrics and insights related to training, learning and development. You will collaborate with area SMEs to ensure that our programs support colleague growth, improve human performance, and enable comfort and proficiency with digital systems/tools. This position will report to the Manager, Learning and Development within the Strategy & Operational Excellence organization and be dedicated to supporting a Focus Factory. It is your dedication and hard work that will make it possible for Pfizer’s customers and patients to receive the medicines they need, when they need them. | 12/08/2025 |
| 45 | Pfizer Pearl River, NY Associate Scientist, Immunology Bachelor’s degree in a relevant scientific discipline (e.g., Biology, Immunology, Biochemistry) Exp: 0-2 years |
As an Associate Scientist in the CMI group, you will play a critical role in generating high-quality cellular immunology data in a regulated laboratory setting to support Pfizer’s vaccine programs. The primary focus of this role is high-throughput flow cytometry to analyze cellular immune responses in clinical and non-clinical samples. You may also support additional immunological assays such as ELISPOT and other biofunctional methods. This position involves routine testing, assay development, and data analysis, all performed in compliance with Good Laboratory Practices (GLP) and internal standards. | 12/08/2025 |
| 46 | Pfizer Rocky Mount, NC Senior Automation Engineer Master's degree Exp: 0+ years |
As a Sr. Automation Engineer your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate explaining difficult issues and establishing consensus between teams. It is your hard work and dedication that will make Pfizer ready to achieve new milestones and help patients across the globe. | 12/08/2025 |
| 47 | Pfizer Sanford, NC EM Analyst I Bachelor’s degree Exp: 0 years |
Conduct and support laboratory operations, including sample preparation, data collection, and analysis. Apply technical skills to assignments, ensuring high-quality results and solving moderately complex problems with sound judgment. Follow procedures with general instructions, maintaining compliance with regulatory standards and working under moderate supervision. Identify activities to support team goals, contributing to overall project success and ensuring adherence to project timelines. Perform testing on clinical and commercial products, raw materials, and validation samples, maintaining a neat and orderly work area. Independently write Standard Operating Procedures, technical reports, project plans, and other documents. Train junior colleagues, develop training plans, oversee training activities, and handle laboratory investigations for events and Out of Stock results. Create, review, and approve compliant test method transfer and validation protocols, reports, and equipment qualification/computer validation records. | 12/08/2025 |
| 48 | Pillar Biosciences Natick, MA Supply Chain Generalist Bachelor’s degree Exp: 0-2 years |
This entry level position plays a critical role supporting supply chain within a fast paced environment. The range of duties include but are not limited to: generating purchase orders for re-order point and MRO items, daily cycle counts, supplier/customer on time order tracking, assisting with international customs documents and picklist as needed. This newly created position requires strong attention to detail and the ability to track data to help drive metric improvements. | 12/08/2025 |
| 49 | Pledge Therapeutics Canton, MA Research Associate, Immuno-Oncology MS Exp: 1-2 years |
We seek an enthusiastic and curious scientist interested in participating in all aspects of the hit-to-lead drug discovery process. The opening is at our new state-of-the-art facility in Canton, MA. The successful candidate will engage in the Immuno Oncology research areas of the company and will work with a successful team of international senior scientists located in the USA and EU. The ideal candidate will have great communication skills, excellent technical skills, exemplary attention to detail, and a passion for learning. This position will have the opportunity to make significant scientific contributions to numerous drug discovery projects. | 12/08/2025 |
| 50 | Pledge Therapeutics Canton, MA Research Associate, Virology Bachelor’s or Master’s degree in biological sciences or a related field Exp: 0-2 years |
We seek an enthusiastic and curious scientist interested in participating in all aspects of the hit-to-lead drug discovery process. The opening is at our state-of-the-art facility in Canton, MA. The successful candidate will engage in the company’s virology research areas and work with a successful team of scientists in the USA and EU. The ideal candidate will have great communication skills, excellent technical skills, exemplary attention to detail, and a passion for learning. This position will have the opportunity to make significant scientific contributions to numerous drug discovery projects. | 12/08/2025 |
| 51 | PROCEPT BioRobotics San Jose, CA Quality Engineer, Sustaining Bachelor’s degree in Engineering (Mechanical, Biomedical, Industrial, or related field), Life Sciences, or equivalent Exp: 1-3 years |
Do you want to be part of an innovative, cutting edge technology, robotics company that is changing how BPH is treated? Are you looking to be part of an enthusiastic, driven, passionate and challenging team, who continuously learn from one another? Are you a leader who wants to make a difference and improve processes? Are you detailed-oriented? At PROCEPT BioRobotics you will have an opportunity to contribute and greatly support our continuous improvement philosophy by being part of our Quality Engineering team. This position has a unique impact on the quality and reliability of our devices. You will work with cross-functional teams to maintain and improve the Quality System within the requirements of FDA's Quality System Regulation (QSR), ISO 13485 (ISO) and EU MDR. Being detail and solution oriented, proactive, and self-managed will assist in the success of this position. | 12/08/2025 |
| 52 | PROCEPT BioRobotics San Jose, CA Reliability Quality Engineer Master’s degree in Mechanical, Biomedical, or Electrical/Electronic Engineering Exp: 1 year |
As PROCEPT BioRobotics continues to expand, the Design Quality Assurance group is seeking a Reliability Quality Engineer to support ongoing reliability initiatives. The Reliability Quality Engineer will collaborate with product development and sustaining teams to ensure that PROCEPT BioRobotics delivers highly reliable products through the application of reliability tools such as Weibull Analysis, Failure Mode Effects & Criticality Analysis (FMECA), Fault Tree Analysis (FTA), structured problem-solving, reliability modeling, reliability predictions, and reliability testing. | 12/08/2025 |
| 53 | Pro-Dex Irvine, CA Manufacturing Engineer Bachelor’s Degree of Science in Mechanical Engineering or related field Exp: 1-2 years |
Works with and across the various disciplines of the engineering team, machine shop personnel, and assembly floor personnel for project realization, manufacturability, inspection, and assembly of product. One of the primary functions of the position is to create, develop, and establish cost effective processes and procedures for manufacturability, inspection, and assembly to reduce cost and improve fabrication methods that meet the product specifications and requirements across various projects. | 12/08/2025 |
| 54 | Profluent Emeryville, CA Research Associate I/II, Platform Discovery BS or MS in molecular biology, biochemistry, or a related field Exp: 0-5 years |
We are seeking a motivated and creative Research Associate I/II to join our Platform Discovery team. You will work closely with more senior team members to evaluate and optimize methods for the delivery of our novel gene editing systems in therapeutically relevant cell types. This includes developing robust high-throughput workflows in biochemical and/or cell-based systems. Your work will be critical for enabling new therapeutic opportunities. The ideal candidate will have extensive experience with molecular cloning, mammalian cell culture techniques, and assay development. This is an excellent opportunity to work cross-functionally with a diverse team of experts across AI and machine learning, protein design, cell biology, and gene editing. | 12/08/2025 |
| 55 | Prolific Machines Emeryville, CA Research Associate II/III, Biology (Contract) Master's degree Exp: 1+ years |
We are looking for a highly motivated and detail-oriented RA II or Sr. RA to drive mammalian cell culture-based protein production workflows at Prolific. We are a team of scientists using light to control the expression of biotherapeutic proteins, increasing titer and improving quality attributes. We are rapidly expanding our capabilities in mammalian cell line engineering, stable cell line generation, and driving production runs to produce therapeutic proteins. You will be instrumental in optimizing and executing cell line development and protein production which will support multiple projects. Your responsibilities will include maintenance and engineering of mammalian suspension cell lines (including CHO), handling, seeding, and sampling runs for protein production, and contributing to downstream readouts such as Octet BLI, flow cytometry, and metabolite measurements (such as Nova). Your knowledge of mammalian cell line development techniques, combined with your attention to detail and motivation to learn will make you highly effective in this role. The ideal candidate for this role is energized by hands-on technical work and takes pride in owning and refining routine cell line generation processes for high quality results. You’ll get to work cross collaboratively with team members in optogenetics, synthetic biology, cell line development, hardware engineering, bioprocessing, and data science disciplines to establish cell lines crucial to Prolific’s success. This is a unique position and opportunity to drive cell culture workflows in an exciting startup setting. You’ll be provided with room for technical growth and receive mentorship to help you succeed. This role is based on-site in our headquarters in Emeryville, CA. The contract is expected to last for 6+ months with the possibility of extension or conversion to full-time employee at the end of the term. | 12/08/2025 |
| 56 | Prolific Machines Emeryville, CA Research Associate II/III, Molecular Biology (Contract) Master's degree Exp: 1+ years |
We are looking for a highly motivated and detail-oriented RA II or Sr. RA to drive molecular biology-based workflows at Prolific. We are a team of scientists using light to control expression of biotherapeutic proteins, increasing titer and improving quality attributes. You will be instrumental in spearheading the top-of-funnel vector development processes which form the foundation for our cell line development pipeline. Your responsibilities will focus around the design and assembly of DNA vectors for downstream cell line engineering applications. Your knowledge of molecular biology techniques, combined with your attention to detail and motivation to learn, will make you highly effective in this role. The ideal candidate for this role is energized by hands-on technical work and takes pride in owning and refining routine molecular biology processes for high quality results. You’ll get to work cross collaboratively with team members in optogenetics, synthetic biology, cell line development, hardware engineering, bioprocessing, and data science disciplines to establish cell lines crucial to Prolific’s success. This is a unique position and opportunity to drive foundational workflows in an exciting startup setting. You’ll be provided with room for technical growth and receive mentorship to help you succeed. This role is based on-site in our headquarters in Emeryville, CA. The contract is expected to last for 6+ months with the possibility of extension or conversion to full-time employee at the end of the term. | 12/08/2025 |
| 57 | Prolific Machines Emeryville, CA Electrical Engineer MSE Exp: 1+ years |
We’re looking for an Electrical Engineer to support design, testing, and integration of electronic systems that power our advanced biomanufacturing platforms. You’ll collaborate closely with hardware, software, and bioengineering teams to ensure our electrical subsystems meet performance, safety, and reliability requirements. This role will be based on-site in Emeryville, CA and will report to the Senior Mechatronics Engineer of the company. Standard hours will be 40hrs per week, with the employee aiming to be onsite during the company’s core hours Monday-Friday, 10am-4pm. | 12/08/2025 |
| 58 | PsychoGenics Paramus, NJ Research Associate 2 Bachelor’s degree in biological sciences neuroscience, or related field Exp: 1-3 years |
We are looking for a highly motivated Researcher to join our neuropharmacology group. The successful candidate will work in a team of scientists and researchers supporting preclinical studies using rodent models. The primary responsibilities of the candidate will include, but are not limited to, dosing animals, surgical nursing, conducting behavioral assessments, and dissection and tissue collection. The candidate will be responsible for coordinating studies and the proper execution of experiments. The candidate must be capable of working both across teams and independently. | 12/08/2025 |
| 59 | Quality Agents Rockville, MD Validation Engineer I BS in a technical discipline (Engineering, chemistry, microbiology, biology) Exp: 0-2 years |
Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. Our Validation specialists will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The validation specialist will evaluate the equipment/utility/system/procedures used in development, production, and holding of pharmaceutical products and determine a validation approach. The individual should have experience with current US and international regulations, guidance, industry best practice in one of the following areas of validation: facilities, utilities, and equipment qualifications, process validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. | 12/08/2025 |
| 60 | Quality Agents Rockville, MD Quality Assurance Specialist BS in a technical discipline (Engineering, chemistry, microbiology, biology) Exp: 0-2 years |
Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. Our Quality Assurance Specialists are leading service providers to our clients providing GMP support. The individual will coordinate validation activities with the client and meet timelines. | 12/08/2025 |
| 61 | Quva Sugar Land, TX Production Technician I - Formulation Bachelor’s degree with an emphasis in Chemistry, Biochemistry or equivalent Exp: 1 year |
Our Production Technician I – Formulation plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical product. Once you complete our training, your responsibilities will include supporting daily manufacturing activities for non-sterile and sterile bulk/CSP operations. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. | 12/08/2025 |
| 62 | Quva Bloomsbury, NJ QC Laboratory Technician Bachelor’s Degree in life science or related field Exp: 1-2 years |
Our QC Laboratory Technician plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include performing basic laboratory support functions related to the management of laboratory samples, materials, and testing supplies. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. | 12/08/2025 |
| 63 | Reckitt Salt Lake City, UT R&D PDM Assistant BS/BA degree in a related science Exp: 0-2 years |
The R&D Operations Assistant will work with technical product development on key projects for the R&D team. | 12/08/2025 |
| 64 | Reckitt Belle Mead, TN Quality Compliance Assistant B.S. degree in a science field required, preferably Chemistry Exp: 0-2 years |
In R&D, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centers of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance. We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality. The size of our organization means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our R&D Academy, designed to develop our team and allow you to grow in our great organization. | 12/08/2025 |
| 65 | Regeneron Tarrytown, NY Process Development Associate, Bioreactor & Scale-Up Development BS or MS in Chemical Engineering or Bio-related Engineering Exp: 0-2 years |
Regeneron’s Bioreactor and Scale-Up Development Group within Preclinical Manufacturing and Process Development (PMPD) is looking for a motivated Process Development Associate to work as part of the late-stage development team to develop production processes of biologics in a non-GMP process development laboratory. In this role, they will perform studies at pilot scale to develop commercially enabling manufacturing processes. | 12/08/2025 |
| 66 | Regeneron Tarrytown, NY Senior Associate Scientist Bachelors degree Exp: 1-4 years |
We are looking for an R&D Associate to join the DNA Core facility. We provide Regeneron laboratories with services vital for conducting scientific research. These services include plasmid preparation and purification. | 12/08/2025 |
| 67 | Regeneron Tarrytown, NY Process Development Associate (PMPD) - Late Stage Cell Culture BS or MS in Chemical Engineering or Bio-related Engineering Exp: 0-2 years |
Regeneron’s Cell Culture Development Group within Preclinical Manufacturing and Process Development (PMPD) is looking for a motivated Process Development Associate to work as part of the late stage development team to develop production processes of monoclonal antibodies in a non-GMP process development laboratory. In this role, they will perform studies at bench scale in support of clinical or commercial manufacturing production. | 12/08/2025 |
| 68 | Regeneron Tarrytown, NY Process Development Engineer I, Analytics (PMPD) MS degree Exp: 0-3 years |
Regeneron's Preclinical Manufacturing & Process Development (PMPD) Analytics group is seeking a Process Development Engineer I interested in the analytical characterization of biopharmaceuticals. In this exciting role, you will conduct analytical experiments that support manufacturing process development and research activities in a fast-paced, high-throughput laboratory setting. | 12/08/2025 |
| 69 | Regeneron Tarrytown, NY Process Development Engineer I - Late Stage Purification (PMPD) Master’s degree in either Chemical Engineering, Biochemical Engineering, Biochemistry, or a related field Exp: 0-3 years |
Regeneron’s Late-Stage Purification Development team within PMPD (Preclinical Manufacturing and Process Development) is seeking a full-time Process Development Engineer I. In this role, you will be responsible for the development and transfer of the harvest, affinity chromatography, and viral inactivation unit operations for recombinant proteins using Quality by Design principles. | 12/08/2025 |
| 70 | Regeneron Tarrytown, NY Process Development Associate - Pilot Scale Purification Development (PMPD) Bachelor’s and/or Master’s degree in either Chemical Engineering, Biochemical Engineering, or Biochemistry Exp: 1-5+ years |
Regeneron's Preclinical Manufacturing & Process Development Group (PMPD) is seeking a Process Development Associate as a full time position to work in the Purification Development group. In this role, you will be responsible for the purification at pilot scale of a variety of clinical biologics, building systems to support the planning and execution of pilot scale work, and investigating technologies to support the scalability of pilot scale operations. The ideal candidate will be hardworking, efficient, flexible, and able to perform key responsibilities in a fast-paced, team environment. This is a lab based role focused on pilot scale operations, requiring a significant amount of physical activity. | 12/08/2025 |
| 71 | Regeneron Tarrytown, NY Associate Scientist, Non Viral Delivery Technologies BS/MS in chemistry, molecular biology, biochemistry, bioengineering, or related field Exp: 0-2+ years |
We are seeking a highly motivated Associate Scientist to join the Non-Viral Delivery Technologies group within Regeneron Genetics Medicines. Our team works closely with all the other teams in the Genetics Medicines group to produce and develop lipid nanoparticles (LNPs) to support their programs. You will work on the LNP production core as well as conduct ligand targeted LNP development work. | 12/08/2025 |
| 72 | REGENXBIO Rockville, MD Associate Scientist, Bioanalytical Lab & QC Support Master’s degree in a relevant scientific field Exp: 1+ years |
As a member of our Bioanalytical Sciences team, you will be responsible for performing nonclinical and clinical sample testing (PK, Immunogenicity, PCR, etc.) following developed, qualified, and/or validated bioanalytical methods in support of REGENXBIO projects and programs. You will also be responsible for developing and validating bioanalytical methods for gene therapy products. You will also be responsible for performing QC review of documentation produced in the Bioanalytical laboratory, including assay runs, summary tables, reports, protocols and collaborate with various departments to ensure compliance with regulatory expectations. | 12/08/2025 |
| 73 | Revolution Medicines Redwood City, CA Safety Scientist MSc in a Life sciences discipline Exp: 1+ years |
The Safety Scientist within Global Patient Safety Science is an individual contributor who provides safety science and pharmacovigilance support to all products across the RevMed portfolio, which includes early and late phase development activities. The individual will be responsible for supporting clinical studies, review of clinical trial protocols, supporting updates to IBs, ICFs, and authoring of DSURs. Additional safety related activities will involve medical review of individual case safety reports (ICSRs), safety surveillance of assigned products and active member of cross-functional teams. | 12/08/2025 |
| 74 | Revvity San Diego, CA Biochemist I - Recombinant Protein Manufacturing Bachelor of Science in in Life Science or related area Exp: 6 months |
BioLegend is seeking a Biochemist I join our recombinant protein manufacturing team. The Biochemist I is responsible for producing recombinant protein products using bacterial cell culture systems. This role involves multiple stages of production, including protein expression, purification, and quality support. Key responsibilities include preparing buffer solutions, culture media, and dilution reagents; performing bacterial cell cultures; purifying recombinant proteins via affinity methods; and conducting DNA isolations following standard operating procedures. | 12/08/2025 |
| 75 | Revvity San Diego, CA Quality Control Associate I, Flow Cytometry (PM Shift) Bachelor’s degree in a scientific discipline Exp: 6+ months |
At BioLegend we are dedicated to commercializing high quality reagents to support the research community for legendary discoveries. The Associate for BioLegend’s Quality Control group will test products such as antibodies and proteins in the following application(s): flow cytometry, immunohistochemistry, western blotting, ELISA, multiplex immunoassays and/or functional bioassays. The candidate will perform all aspects of the assays following SOPs and ISO requirements. Additional responsibilities include culturing mammalian cell lines, isolating primary cells, and maintaining laboratory equipment and supplies. We are looking for a highly motivated person who loves science and wants to be part of a dynamic and fast paced team. | 12/08/2025 |
| 76 | Rion Rochester, MN Research Associate, Analytical Development Bachelor’s or Master’s degree with focus in Biological Sciences Exp: 1+ years |
The Analytical Development Research Associate will contribute to analytical method development, implementation, and pre-qualification of methods focused on Rion’s exosome technology. This role will work closely with Rion Quality Control to execute method transfers and support continuous improvement. As such, the candidate will possess the technical skills required to conduct experiments and assays in a wet lab environment involving techniques such as mammalian cell culture, ELISA, RT-qPCR, HPLC and colorimetric/fluorometric-based assays. The Analytical Development Research Associate will be responsible for the execution of experiments, as well as data interpretation and final reporting. The position affords the opportunity to serve as a key member of Rion’s scientific team and contribute to the advancement of exosome therapeutics. The Analytical Development Research Associate will work closely with the Analytical Development Scientists and support the efforts of Quality Control/Process Development. As such, the successful candidate will work in an upbeat, highly collaborative and dynamic environment. Additional responsibilities associated with this position will involve assisting in day-to-day laboratory operations such as inventory management, procurement, and general laboratory and equipment maintenance. | 12/08/2025 |
| 77 | Sanguine Biosciences Los Angeles, CA Apheresis Operations Specialist I Bachelor's Degree in a life science or other related field Exp: 1-2 years |
The role of the Apheresis Operations Specialist I is to serve as a primary point of contact for both our donors participating in apheresis collections and our partner site contacts. The AOS I is responsible for screening and qualifying donors who are part of an extensive Sanguine database, and those who are identified by the Patient Recruitment and Marketing Team. The AOS I will screen potential donors to obtain the necessary health information, conduct medical record reviews to qualify donors for apheresis research studies, and provide a seamless experience for our donors. The Apheresis Operations Specialist is also responsible for collecting all necessary documents, coordinating with apheresis sites to schedule donors and pick up services, maintaining patient data and documenting results, fielding real-time calls and emails, and striving to provide a seamless experience for our donors. This individual will be a part of our Apheresis Operations team and will work cross-functionally with multiple departments including Project Management, Patient Operations, and apheresis site points-of-contact. | 12/08/2025 |
| 78 | Sanguine Biosciences San Diego, CA Laboratory Technician I Bachelor’s degree Exp: 1 year |
The Entry Level Lab Technician I will be responsible for the processing and testing of various blood samples. Sample processing will include, but is not limited to: PBMC, T, B, & NK cell isolations. Other assigned duties may include cell counting, aliquot preparation, accessioning, reagent creation, proper storage, flow cytometry lab services. Initial samples will be from both Leukopaks and blood samples or its derivatives. This role will also require experience with LIMS systems and commercial laboratory operations, including the internal communication of project details with Sanguine personnel as well as the ability to work as a team. | 12/08/2025 |
| 79 | Science 37 Morrisville, NC Supply Associate Bachelor’s degree Exp: 1 year |
The Supply Associate position is responsible for assisting with the management of clinical supplies and equipment used in clinical studies. The Supply Associate is responsible for preparing and shipping study supplies to study participants and study staff, maintenance and accountability of study supplies and nursing equipment, ordering of supplies, and inventory management. The Supply Associate works closely with the Supply team, PI, sub-Is and study team to ensure safe and efficient conduct of clinical studies. | 12/08/2025 |
| 80 | Serán Bend, OR Scientist/Engineer, Drug Product Development Bachelor or Master’s degree in pharmaceutical science, chemistry, chemical engineering, biological engineering, mechanical engineering, materials scie Exp: 1 year |
Serán seeks to hire a Scientist/Engineer to join the Drug Product Development group and contribute as part of an interdisciplinary team to develop and scale-up pharmaceutical manufacturing processes. The role requires strong hands-on laboratory skills and the ability to apply fundamental scientific principles to solve problems. Strengths in data collection, analysis, proactive communication, and continuous learning by textbooks, journals, and training will enable the successful candidate to thrive. The ideal candidate would enjoy a work environment that is both science-focused and adaptable to meet | 12/08/2025 |
| 81 | Serán Bend, OR Associate I, Sample Management Coordinator Bachelor’s degree in a scientific discipline Exp: 1 year |
Serán BioScience is searching for an organized and detail oriented Associate to support the Sample Management Program within the Quality Control Department. The QC Associate I, Sample Management Coordinator plays a key role supporting sample coordination by managing sample inventory, including the receipt, handling, shipment, and storage of samples supporting the GMP retention program, stability program, and external Contract Testing Laboratories (CTL) testing. All necessary training provided. Those with an interest in starting a career in bioscience are encouraged to apply. | 12/08/2025 |
| 82 | NorthStar Beloit, WI Radiopharmaceutical Manufacturing Associate Bachelor's Degree in a STEM discipline Exp: 1 year |
The Radiopharmaceutical Manufacturing Associate performs duties to support the development and manufacturing of radiopharmaceuticals for NorthStar operations. This includes equipment preparation, product dissolution, and dispensing of medical radioisotopes while complying with procedures, instructions, and prescribed routines. All duties and responsibilities will be completed in compliance with applicable regulatory agency standards. | 12/01/2025 |
| 83 | Nuclein Austin, TX Technical Applications Specialist I Bachelor’s degree in a relevant field (Biology, Molecular Biology, or similar discipline) Exp: 1-2 years |
Position objective is to provide a high degree of direct support to end-user customers with the primary goal of ensuring on-going customer satisfaction. Accomplished by providing a high level of rapid and complete customer service through answering inquiries, problem resolution, customer communication and ensuring correct internal response to customer identified potential or actual issues which could impact the safety and efficacy of Nuclein provided products. | 12/01/2025 |
| 84 | Oakwood Labs Solon, OH Quality Control Chemist Bachelor's degree in Chemistry, Biochemistry, Biology, or related field Exp: 1-2 years |
Perform analytical testing of raw material, in-process product, final product release and stability testing. Clear documentation of test activities in approved worksheets and laboratory notebooks. Execute mathematical calculations as outlined in test methods. Assess data to determine if the material tested meets specifications. Peer review of quality control data. Participate in investigational testing and assist with root cause analysis. Create and review SOP’s and author Change Controls. Other general lab related duties as necessary. | 12/01/2025 |
| 85 | Obsidian Therapeutics Bedford, MA Research Associate, Process Development BS or MS degree in chemical engineering, biochemical engineering, biology or relevant field Exp: 0-2 years |
We’re looking for a highly motivated, flexible, and collaborative Research Associate with experience in, and a passion for—cell culture and process development. Based at our Bedford, MA location, you’ll contribute to developing and characterizing manufacturing processes for cell therapy products targeting cancer. You’ll be a vital part of a highly collaborative Technical Operations team, working to achieve Obsidian’s vision by translating innovative science into medical breakthroughs for patients, starting with our lead program, OBX-115—a novel engineered tumor-infiltrating lymphocyte (TIL) therapy. | 12/01/2025 |
| 86 | Olympus San Jose, CA Repair Engineer I Bachelor's degree in engineering Exp: 1 year |
Provide engineering support for introduction of new products and alternate repair activities. Function as Project Coordinator on more complicated projects as defined by the Manager by providing technical information to other project participants recommending cost effective procedures tracking and maintaining implementation dates and documenting completed projects. Provide support to Associate Engineer on his/her assigned projects. | 12/01/2025 |
| 87 | Orca Bio Sacramento, CA Cell Therapy Production Associate, Oncology B.S. degree in Biological or related sciences Exp: 1 year |
The Cell Therapy Production Associate, Oncology plays a critical role in the production of Orca Bio’s life-saving cell therapy products, ensuring adherence to strict quality standards, regulatory requirements and aseptic production techniques. Reporting into the assigned supervisor, commercial manufacturing, the job involves repeatedly executing manufacturing processes, cleaning and maintaining production equipment and workstations and documenting production activities in a highly regulated environment. The role collaborates closely with Materials Management, Quality Control (QC), and Quality Assurance (QA) to carry out GMP manufacturing runs as part of a cross-functional team. | 12/01/2025 |
| 88 | Orchid Orthopedic Solutions Bridgeport, MI Quality Engineer, Sustaining Product Quality Bachelor of Science (B.S) Exp: No exp |
The Quality Engineer I supports the ongoing quality of Orchid's legacy products & processes and works cross-functionally to sustain the business. | 12/01/2025 |
| 89 | OrganaBio Irvine, CA On-Call Cell Processing Associate Bachelor Degree in Biology, Cell and Molecular Biology, Biotechnology, Biomedical Engineering, or related field Exp: 1-2 years |
A Cell Processing Associate assists in the performance of primary peripheral blood mononuclear cells (PBMCs) isolation from patient samples, as part of screening efforts for various customers. This position will help contribute to PBMC isolation process improvement, to drive efficiency in the documentation and production process. This role will support Process Development (PD) team efforts, and interact cross-functionally with teams that include, but are not limited to Business Development and Quality Assurance, to ensure company milestones are met. This position will ensure that products are processed under GLP practices, with appropriate documentation in place, it will also interact with external customers for which samples are processed, assuring that such communication is clear and disseminated in time, and processed samples are shipped back to customer, according to customer timeline. | 12/01/2025 |
| 90 | Organogenesis Canton, MA Production Associate I - Apligraf (Sunday-Thursday) Bachelor’s degree in biology or related science Exp: 0-2 years |
This is an entry level position. The Associate will perform all activities involved in the aseptic processing of a living product (Apligraf), under the direct supervision of the Apligraf Team Leader/Apligraf Supervisor/Manager. The Apligraf Associate I will support the Apligraf Manufacturing department by performing the tasks that will assure the safe and timely processing of Apligraf, working in both a Class 100 and Class 10K cleanroom. | 12/01/2025 |
| 91 | Organogenesis Canton, MA QC Analyst I/II -Microbiology BS degree in a Microbiology or related field Exp: 1+ years |
Perform routine quality control microbiology activities in support of product production and releases. The position interacts with other internal departments, including Apligraf Production, PuraPly Production, Quality Assurance, Validation, Calibration, Materials, and Logistics. The position may interact with external entities including contractors and suppliers. The QC Analyst I/II performs a wide variety of routine activities to ensure compliance with applicable regulatory requirements by conducting testing, trending, and reporting result. | 12/01/2025 |
| 92 | Organogenesis Smithfield, RI Production Associate Dermagraft Bachelor’s degree in biology or related science Exp: 0-2 years |
This is an entry level position. The Associate will perform all activities involved in the aseptic processing of a living product (Dermagraft), under the direct supervision of the Dermagraft Team Leader/Dermagraft Supervisor/Manager. The Dermagraft Associate will support the Dermagraft Manufacturing department by performing the tasks that will assure the safe and timely processing of Dermagraft, working in both a ISO 7 and ISO 8 cleanrooms. | 12/01/2025 |
| 93 | Pace Analytical Oakdale, MN Experienced Pharma Analytical Chemist Bachelor's degree in Chemistry, Biochemistry, Analytical Chemistry, or a related scientific discipline Exp: 0-2 years |
The Scientist I will contribute to laboratory operations by performing analytical testing, interpreting data, and maintaining laboratory equipment and documentation in accordance with established protocols and quality standards. | 12/01/2025 |
| 94 | Pace Analytical Portsmouth, VA Analytical Chemist BS degree in Chemistry, Biology, Biochemistry, or a related degree Exp: 1-2 years |
A candidate for this role will support an organics laboratory in environmental services and equipment management. | 12/01/2025 |
| 95 | Pace Analytical Lebanon, NJ PLS QA Specialist I Bachelor's degree in chemistry, operations, or a closely related field Exp: 1-2 years |
Responsible for providing advanced oversight of the analysis and administration of various quality policies, programs, and practices in accordance with current Good Manufacturing Practices (cGMP); provides feedback, direction and guidance to employees and management, using advanced professional and technical knowledge of quality or related equipment, testing, and procedures. | 12/01/2025 |
| 96 | Pace Analytical Cleveland, OH Entry Level Chemical Regulatory Analyst Bachelor of Science (Chemistry, Engineering, or related field) Exp: 1-2 years |
This position is part of a team that gathers, analyzes, and reports packaging, post-consumer recycling, and plastic data to various government agencies, frequently through third party Producer Responsibility Organizations, in the US and Canada. The team is part of a larger group that supports regulatory and compliance activities. The candidate may also support activities of the larger group. Candidate will contact suppliers to request packaging data, collect the packaging information, and organize/format data for use in various reports. They will also review data collection and organization processes to document procedures for various activities of the group. For on-site materials that need physical weight determinations, they may need to work in a laboratory setting using appropriate measuring equipment to record weights. Candidate may also assist with Federal Plastics Registry reporting as needed. Organizational skills and the ability to work independently are required for this role. Skills related to data manipulation and the ability to use various Microsoft Office (and potentially other software applications such as Business Objects, MicroStrategies, OnBase, etc.) while working with large sets of data will be integral to the role. We are looking for a team player who is self-motivated, able to maintain high quality while handling repetitive tasks, and manage multiple projects for different stakeholders. | 12/01/2025 |
| 97 | Pall New Port Richey, FL Manufacturing Engineer Bachelor’s degree in Manufacturing, Mechanical, Industrial, Aerospace, or related Engineering field Exp: 1 year |
The Manufacturing Engineer is responsible for driving improvements across assigned value streams to meet Safety, Internal and External Quality, on-time delivery, lead time reduction, and Productivity. This role is a key part of the Value Stream leadership team, responsible for driving daily performance and leading data-driven, root-cause-based action plans to achieve breakthrough KPIs through LEAN (DBS) tools and continuous improvement. This position reports to the Operations Manager and is part of the Value Stream leadership team, located in New Port Richey, FL. It will be an on-site role. | 12/01/2025 |
| 98 | Parexel West Point, PA Scientist III - Analytical Chemist - High-Throughput Purification Support MS Degree in Chemistry, Biochemistry, or closely related field Exp: 1-2 years |
We are looking to fill a Scientist III – Analytical Chemist - High-Throughput Purification Support position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in West Point, PA. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. | 12/01/2025 |
| 99 | Parexel West Point, PA Scientist III - Biophysical & Materials Analytical Characterization - FSP MS in chemistry, biology, or related field Exp: 1-2 years |
This is a laboratory-based scientific role in a fast-paced, multidisciplinary team environment, requiring the utilization of biophysical analytical characterization techniques to support development of vaccine drug substance and drug products in a GMP-like environment. The vaccine drug substance and product development support includes sample manipulation, equipment maintenance, routine analysis, and characterization of development vaccines to support process and formulation development. | 12/01/2025 |
| 100 | Parexel Rahway, NJ Scientist III - (HPLC) Chromatography - Separations & Molecular Biology - Immunoassay Experience - FSP MS Exp: 1-2 years |
Support of routine bioanalytical testing of samples from cell-line development, in-process, process development/characterization, forced degradation, release & stability, and pre-formulation. Other potential opportunities include method development/optimization, workflow optimization, and template development. | 12/01/2025 |
| 101 | Parexel Rahway, NJ Scientist II or III – Analytical Chemist Metrology Specialist B.S./M.S. in Chemistry, Biochemistry, Engineering, or a related discipline Exp: 1-2 years |
Metrology specialist is responsible for the oversight of regulated and non-regulated laboratory equipment. This role will oversee the lifecycle of the lab instrumentation covering acquisition and installation, performance or coordination of routine maintenance, computer system validation, and regulated systems retirement. | 12/01/2025 |
| 102 | Parexel West Point, PA Scientist II or III - Metrology Specialist - FSP B.S./M.S. in Chemistry, Biochemistry, Engineering, or a related discipline Exp: 1-2 years |
The Metrology Specialist is responsible for the oversight of regulated and non-regulated laboratory equipment. This role will oversee the lifecycle of the lab instrumentation covering acquisition and installation, performance or coordination of routine maintenance, computer system validation, and regulated systems retirement. | 12/01/2025 |
| 103 | Parexel Rahway, NJ Scientist III - Analytical Chemist - FSP MS degree Exp: 1-2 years |
We are looking to fill a Scientist 3 - Analytical Chemist position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in Rahway, NJ. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer any sponsorship. | 12/01/2025 |
| 104 | Parexel West Point, PA Scientist III - Analytical Chemist - Drug Product MS degree Exp: 1-2 years |
We are looking to fill a Scientist 3 - Analytical Chemist - Drug Product position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in West Point, PA. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer sponsorship. | 12/01/2025 |
| 105 | Parse Biosciences Seattle, WA Quality Control Associate I Bachelor’s degree in Molecular Biology, Biochemistry, or related biological sciences Exp: 6 months |
As a Quality Control (QC) Associate I, you will work as part of the Quality Control team to test and verify that all raw materials and finished goods meet defined specifications for quality, consistency, and performance. In this role, you will test our manufactured products against established standards and release criteria, ensuring our customers receive high-quality, conforming reagents. We are looking for candidates who are highly self-motivated, eager to expand their technical expertise, and committed to their team’s success in a fast-paced environment. | 12/01/2025 |
| 106 | PCI Bedford, NH QC Chemist I Bachelor of Science in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study Exp: 0-3 years |
This position will have responsibility to support various activities in the Quality Control Laboratory. This includes testing the following sample types R&D, in-process, finished product, stability, as well as raw materials. Job duties may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management. | 12/01/2025 |
| 107 | PCI Madison, WI QA Associate I - Operations Bachelor’s degree in a relevant scientific field Exp: 0-2 years |
Are you eager to build your career in pharmaceutical manufacturing while making a meaningful impact on product quality and patient safety? Join us at PCI as a Quality Associate I – Operations, where you’ll be on the front lines of GMP production—supporting real-time quality oversight, solving problems as they arise, and ensuring that every product meets the highest standards of safety, efficacy, and compliance. | 12/01/2025 |
| 108 | PCI Madison, WI QC Chemist I Bachelor of Science in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study Exp: 0-3 years |
This position will have responsibility to support various activities in the Quality Control Laboratory. This includes testing the following sample types R&D, in-process, finished product, stability, as well as raw materials. Job duties may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management. | 12/01/2025 |
| 109 | PCI Madison, WI Plant Engineer I BS in Chemical, Mechanical, or other Engineering degree Exp: 0-2 years |
The Plant Engineer I provides engineering support throughout the various manufacturing facilities in areas such as process equipment improvements, technological advancements, capital projects, existing manufacturing equipment, cost improvements, facility maintenance, safety and environmental regulation. Demonstrate good engineering, effective collaboration, partnering and teamwork skills when interacting with internal and external resources. | 12/01/2025 |
| 110 | PCI Philadelphia, PA Process Engineer Bachelor’s degree in mechanical, chemical, biomedical, packaging engineering, or a related field Exp: 1-5 years |
PCI is seeking a motivated and detail-oriented Process Engineer I to provide technical leadership in new product launches and continuous improvement initiatives. The ideal candidate will focus on mitigating packaging issues, optimizing production processes, and supporting operational efficiency. This role will involve providing technical and operational support to production, maintenance, and support teams, particularly in the areas of process improvement, equipment modification, optimization, safety, and quality improvement. The Process Engineer I will utilize lean and six sigma techniques and demonstrate excellent organizational and leadership skills in managing projects, equipment needs, staffing projections, and line layout. | 12/01/2025 |
| 111 | PCI Philadelphia, PA Facilities Engineer I Bachelor's Degree in a related field Exp: 1-5 years |
Facilities Engineer I estimates costs related to layout design, including equipment and materials, labor, etc. and monitors the construction process. Plans and implements the design of plants, offices, and production lines to maximize the use of available space and improve production efficiency. Ensure that established efficiency and safety targets are met. Research facilities equipment or fixtures for purchase and gather data relating to their ability to meet organizational needs. Works on projects/matters of limited complexity in a support role. Work is closely managed. | 12/01/2025 |
| 112 | PCI Rockford, IL Project Engineer- Drug Delivery Bachelor’s degree in Mechanical, Biomedical, Chemical, or related Engineering discipline Exp: 1-5 years |
As a Project Engineer – Drug Delivery, you’ll play a hands-on, critical role in the design, development, and execution of pharmaceutical packaging and assembly projects. Working closely with engineering, quality, and validation teams, you’ll help deliver high-impact solutions that directly affect patient outcomes around the world. This role supports key product introductions - including high-speed auto-injector lines for diabetes management—giving you the opportunity to work on cutting-edge drug delivery technology. You’ll collaborate with both internal stakeholders and external customers, ensuring projects are delivered on time, on budget, and in compliance with all regulatory standards. This is more than a role—it's a career path. Our Project Engineers have advanced to senior-level roles, including Engineering Manager, based on performance, innovation, and leadership. | 12/01/2025 |
| 113 | Penumbra Alameda, CA Manufacturing Engineer I - Electronics Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering or related degree Exp: 1+ years |
The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and that support continuous improvement in production. Project opportunities are designed to develop professional work knowledge and abilities and to support the efforts and projects that have global importance to the success of the business. Area of work involves manufacturing processes with interaction between production and cross-departmental engineering groups in resolving problems encountered on the production floor and across the business. Evaluates, selects, and applies exciting engineering techniques, procedures, and criteria, using judgment in developing and implementing adaptations and modifications on the production line and to quality systems. | 12/01/2025 |
| 114 | Penumbra Alameda, CA Manufacturing Engineer II - Equipment Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, Industrial Engineering, or related degree Exp: 1+ years |
The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and that support continuous improvement in production. Project opportunities are designed to develop professional work knowledge and abilities and to support the efforts and projects that have global importance to the success of the business. Area of work involves manufacturing processes with interaction between production and cross-departmental engineering groups in resolving problems encountered on the production floor and across the business. The Manufacturing Engineer Equipment II specializes in the design, development, evaluation, selection, and ordering of the equipment that is most appropriate and cost-effective for the manufacture of company products. Evaluates, selects, and applies exciting engineering techniques, procedures, and criteria, using judgment in developing and implementing adaptations and modifications on the production line and to quality systems. | 12/01/2025 |
| 115 | Penumbra Alameda, CA Manufacturing Engineering Manager - Metals/Catheters Master’s degree in an engineering or related technical field Exp: 1+ years |
Provide management in the engineering, design and development of new products or changes to existing products, processes, and equipment. Direct the transfer and scale-up of products from R&D to Production. Exercise judgment within generally defined practices and policies in determining project plans (milestones, resources) and selecting methods and techniques for meeting project goals. | 12/01/2025 |
| 116 | Penumbra Alameda, CA Supplier Quality Engineer I Bachelor’s degree in engineering, science, or a related field Exp: 0-3 years |
As a Supplier Quality Engineer I at Penumbra, you will play a key role in ensuring our supply chain consistently delivers components and materials that meet the highest standards of quality and compliance. Working closely with cross-functional partners in Operations, Compliance, and R&D, you will support supplier qualifications, changes, corrective actions, and performance monitoring. You’ll help resolve supplier-related issues, drive improvements, and ensure adherence to Penumbra’s Quality Management System (QMS) and regulatory requirements. This is an excellent opportunity for an early-career engineer to build a strong foundation in supplier quality, gain exposure to medical device manufacturing, and grow within a high-impact quality organization. You’ll join a collaborative and growing Quality organization that invests in technical development and career growth. | 12/01/2025 |
| 117 | Penumbra Alameda, CA Quality Monitoring & Improvement Specialist I Bachelor's degree preferably in engineering, life sciences, or a related field Exp: 1+ years |
As a key member of the Quality team, you will have a hand in ensuring that Penumbra's life-saving products adhere to the highest standards of quality and safety. In the Quality Monitoring & Improvement Specialist I role, you will be supporting our Quality Management System (QMS) processes, specifically Corrective and Preventive Actions (CAPAs), Nonconformance Reports (NCRs) and Deviation Authorizations (DAs) following Penumbra's procedures and regulatory requirements. You will organize and host board meetings to facilitate board review of documentation supporting these systems. You will also assist with data compilation for monthly trending meetings. | 12/01/2025 |
| 118 | PerkinElmer Washington, DC Senior Project Engineer I, PF Services Bachelor’s Degree in Life Science, Engineering, or related discipline Exp: 1-2 years |
The Project Engineer is a fully billable role that will work collaboratively with clients, vendors, contractors, and other Team Members to support projects related to biomanufacturing across the entire engineering lifecycle. The Project Engineer is responsible for delivering high quality work, forming and maintaining valuable, long-term relationships with our clients, and continually strengthening their technical and industry knowledge. They will maintain a strong focus on Project Farma’s Patient Focused and People First mindset. | 12/01/2025 |
| 119 | Perrigo Eau Claire, WI Associate R&D Process Scientist Bachelor’s degree in Food or Dairy Science, Chemical or Food Engineering, Chemistry or closely related Exp: 1-3 years |
Perrig is currently hiring for an Associate R&D Process Scientist to lead scale-up of new infant formulas from development to full-scale production, overseeing change control, risk assessment, and factory trials while collaborating with cross-functional teams including Product Development, Pilot Plant, Operations, Quality, and Planning. Support manufacturing sites on continuous improvement opportunities in recipe and processing, driving optimization and renovation initiatives through root-cause analysis, cross-functional collaboration, and execution of cost-reduction strategies while ensuring compliance and operational excellence. Develop and implement new process capabilities via feasibility trials and continuous improvement projects to enhance efficiency, reduce costs, and improve overall product quality. | 12/01/2025 |
| 120 | Perrigo Bronx, NY QC chemist II - Days Bachelor of Science degree in a scientific discipline (Chemistry or Food Science preferred, Biology) Exp: 1-2 years |
To ensure the Quality and Compliance of raw materials, finished products, and stability samples by performing laboratory analytical testing relative to the support of Perrigo operations and manufacturing needs. Responsible for preparing solutions and reagents for testing as required. Uses analytical laboratory equipment such as HPLC, UPLC, GC, UV and IR. Works independently and within team under direction of supervisor to accomplish tasks. | 12/01/2025 |
| 121 | Personalis Fremont, CA Sample Accessioner 1 (Temp) Bachelor of Arts or Science Exp: 0-2 years |
This role offers the opportunity to gain experience in a fast paced cutting edge clinical lab environment. The Sample Accessioner will work in a team environment which includes project managers and clinical lab ops specialists. As an Accessioner, daily tasks will involve patient specimen intake, accessioning and fulfilling client requests for returns or destructions. This will entail following SOPs and working with Laboratory Information Management System (LIMS) and other software. This role will also perform shipping / receiving, recording and inventorying of samples sent for laboratory testing. | 12/01/2025 |
| 122 | Legend Biotech Raritan, NJ QC Technical Trainer III Bachelor’s Degree in Science, Engineering or equivalent technical discipline Exp: 0-2 years |
The QC Technical Trainer is an exempt level position working within QC Microbiology training team. This individual will be responsible for performing training activities for Quality Control Microbiology team members who support cGMP Clinical and Commercial Cell Therapy testing. This role will require technical experience, effective communication, coordination, and collaboration across relevant cross functional groups to enable robust testing and release of products to patients. This position is primarily a M-F schedule, with potential nights or weekends temporary coverage as needed. | 11/24/2025 |
| 123 | Legend Biotech Somerset, NJ Associate Scientist Bachelor’s degree in biotechnology, Bioengineering, Molecular Biology, or related discipline Exp: 1-2 years |
We are seeking a motivated Associate Scientist to join our MSAT team, supporting the development, troubleshooting, and optimization of automated manufacturing processes for CAR-T and other cell therapy products. Under the guidance of senior staff, this role will perform bio-pilot run experiments, technology evaluations, and process improvement studies. The position will directly contribute to manufacturing robustness and efficiency by executing laboratory work, assisting in equipment testing, and analyzing process data. | 11/24/2025 |
| 124 | Legend Biotech Raritan, NJ Operations Associate Bachelors Degree required in Life Sciences Exp: 0-2 years |
This position is responsible for performing manufacturing procedures and the execution of scheduled tasks within a CGMP environment. This position is responsible for quality and maintaining the highest standards in compliance within company policies, procedures, and all applicable regulations. | 11/24/2025 |
| 125 | Legend Biotech Raritan, NJ QC Analyst I Bachelor’s Degree in Science, Engineering or equivalent technical discipline Exp: 1 year |
The QC Analyst is an exempt level position with responsibilities for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment. | 11/24/2025 |
| 126 | Legend Biotech Somerset, NJ Senior Research Associate/Associate Scientist (Contractor) MS in Biology or related field Exp: 1+ years |
We are seeking a highly motivated and detail-oriented Bioassay research scientist to join our Bioanalytical team. The ideal candidate will bring technical expertise in molecular assays (qPCR/ddPCR), multi-parameter flow cytometry and contribute to the daily operations of the lab supporting both clinical and preclinical research. This role requires strong organizational skills, the ability to collaborate effectively with cross-functional teams, and a background in biology or a related field. The successful candidate will play a critical role in ensuring the accuracy, reproducibility, and integrity of experimental data. | 11/24/2025 |
| 127 | LGC Petaluma, CA Oligo Manufacturing Technician I Bachelor's degree in a related field Exp: 1 year |
The Oligo Manufacturing Technician I is responsible for supporting Molecular Biology Conversion manufacturing in an ISO 9001 (Custom RUO) and/or ISO 13485 (DxGMP) regulated environment. This position performs production procedures in compliance with current Good Manufacturing Practices (cGMP) (ISO 13485), Standard Operating Procedures (SOPs), and applicable regulatory standards. The technician will work closely with cross-functional teams to deliver high-quality oligonucleotide products for research or diagnostic applications. | 11/24/2025 |
| 128 | LGC Petaluma, CA Chemistry Technician I/II Bachelor’s Degree in a Physical Science Exp: 0-2 years |
This role is responsible for the manufacturing of Controlled Pored Glass (CPG) materials by following established and robust protocols. This position will primarily work with solid phase chemistry that is used in oligo manufacturing. CPG material manufacturing includes amine and nucleoside modification of native CPG at various angstrom sizes as well as modification with proprietary dyes and quenchers. The Chemist I will also be responsible for the upkeep of basic CPG equipment used in these processes. | 11/24/2025 |
| 129 | LGM Pharma Rosenberg, TX Quality Assurance Specialist Bachelor’s degree in a scientific discipline or equivalent Exp: 1+ years |
Performs initial, in-process and final inspections during manufacturing/packaging of product; resolves inspection findings with Packaging Manager and/or QA Manager. Collects product samples for product release testing, process validation testing and product stability as applicable and prepare labels at completion of packaging. Prepares documentation and forward samples to QC Lab for required testing; records information on batches in-process of testing on QC board; notifying QC of any urgent testing. Monitors incoming materials as received in Quarantine. Reviews material received paperwork and compare to material received for accuracy; notifying Materials Department to call supplier if CofA has not been received or CofA is incomplete. Coordinates with production areas to anticipate material usage to meet required schedule. Prepares required approval documentation for component or raw material inspection or testing. Collects raw material samples, label and forward with appropriate documentation to QC lab. Reviews lab data and approve/reject raw materials for use in production. | 11/24/2025 |
| 130 | Locus Biosciences Morrisville, NC Associate Quality Specialist Bachelor’s Degree in Biology, Chemistry, Life Sciences or Engineering Exp: 1 year |
Locus Biosciences is seeking a full-time Associate Quality Specialist. This individual will directly report to the Associate Director of Quality and will be responsible for leading, supporting and ensuring continued suitability of the Quality Management System (QMS) with a primary focus on design control, validation, risk management, supplier management, process control, post-market surveillance, complaint handling, CAPA, auditing, change control, document control and training. | 11/24/2025 |
| 131 | Lubrizol Brecksville, OH Laboratory Specialist Bachelor’s Degree in Engineering or related technical discipline Exp: 1+ years |
As a Technical Specialist, you will be an integral part of our dynamic R&D Laboratory. The ideal candidate will possess the ability to work collaboratively with our scientists and engineers to address and resolve a diverse range of technical challenges. The successful candidate will exemplify a strong commitment to the safe and efficient operation of our laboratories, which encompass both thermal processing equipment and sensitive analytical instruments. | 11/24/2025 |
| 132 | Lumos Pharma Remote, Clinical Quality Assurance Specialist Bachelor's Degree in Biology, Chemistry, Health Administration, or related technical discipline Exp: 1-3 years |
This position reports to the Vice President, Quality and Compliance, and is responsible for providing quality oversight of clinical trial activities performed in compliance with Good Clinical Practices (GCP). This position also supports internal quality systems and compliance functions. The Clinical Quality Assurance Specialist is expected to execute established processes involving quality assurance, quality systems, and compliance. | 11/24/2025 |
| 133 | MannKind Danbury, CT Engineer II, Validation MS in a technical discipline Exp: 1-3 years |
The Engineer II, Validation understands validation methodology and can apply it to process, packaging, equipment, and cleaning activities. Generates and executes validation protocols with limited supervision. Adheres to validation schedules. | 11/24/2025 |
| 134 | MannKind Danbury, CT Specialist I, Quality Assurance BA/BS degree in a scientific or technical discipline Exp: 1-2 years |
Ensures processes and products conform to established company and regulatory standards. Reviews, analyzes and reports on quality discrepancies related to manufacturing and testing of product and company systems. Investigates problems and recommends disposition and corrective actions for recurring discrepancies. Uses predetermined methods, operations and procedures to inspect and test raw materials, work-in-process, finished product as applicable. | 11/24/2025 |
| 135 | Mariana Oncology Watertown, MA SRA I/II, Bioanalytical Sciences Master’s degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or relevant scientific discipline Exp: 1+ years |
We are seeking an experienced Senior Research Associate I/II, Bioanalytical Sciences to join Mariana’s Preclinical Development organization, advancing personalized medicine and radiopharmaceuticals. This laboratory-based position will play a key role in conducting LC-MS-based bioanalysis to support pharmacokinetic (PK), in vitro ADME, and proteomics studies across preclinical programs, focusing on sample preparation, method execution, and data collection. The successful candidate will contribute directly to the development of novel therapeutics by generating high-quality quantitative and qualitative bioanalytical data. | 11/24/2025 |
| 136 | Masimo Irvine, CA Operations Analyst Bachelor’s degree, preferably in Engineering related fields Exp: 1-3 years |
The Operations Analyst will play a key role in enabling the company’s Operations to function by leveraging state of the art processes, tools, and methods. | 11/24/2025 |
| 137 | Matica Bio College Station, TX Validation Engineer I Bachelor`s Degree in a Life Science, Engineering or related science discipline Exp: 1-2 years |
The Validation Engineer I is an entry level position and will support the efforts of the Validation department. | 11/24/2025 |
| 138 | Meissner Camarillo, CA Associate Scientist I Bachelor's degree (BS) in chemistry, biology, or related subject Exp: No exp |
The Associate Scientist I, under direct supervision, supports laboratory testing activities focused on pharmaceutical filtration and analytical studies. This role involves performing routine tests as well as conducting analytical tests. The role includes maintaining laboratory equipment, records, and cleanliness, while adhering to established procedures and safety protocols. | 11/24/2025 |
| 139 | Merck Elkhorn, NE Quality Control Technician Bachelor's degree in a technical scientific discipline Exp: 1+ years |
Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement. We work in the local plant connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates, and finished products. | 11/24/2025 |
| 140 | Microbiologics Saint Cloud, MN Manufacturing Science Associate Bachelor’s degree in a relevant field (e.g., Biology, Microbiology, Molecular Biology, or related discipline) Exp: 1-3 years |
We are looking to add two (2) Manufacturing Science Associate's to our R&D Team in St. Cloud, MN. In this role the Manufacturing Science Associate will be supporting the development, validation, and continuous improvement of manufacturing processes throughout the product lifecycle. This role bridges research and production—transforming innovative product designs into scalable, high-quality manufacturing processes. The ideal candidate will apply scientific and technical expertise to drive efficiency, ensure compliance, and uphold rigorous documentation and integrity standards. | 11/24/2025 |
| 141 | MilliporeSigma Bedford, MA Scientist 1 - Analytical Chemistry Bachelor’s or Master's degree in Chemistry, Biology, Chemical Engineering, Biomedical Engineering or other Science or Engineering field Exp: 1+ years |
Join our team at MilliporeSigma as a Scientist 1 in Bedford, MA. In this role, you will be part of the Analytical team that focuses on the development, optimization and performance of analytical methodology supporting research and development of new products and their manufacturing processes. Your role will be to perform extractables studies, and to determine compounds that can be released or migrate from single-use and filtration devices and other MilliporeSigma products, using TOC, HPLC, GCMS, ICP, ion chromatography, LCMS, and other appropriate characterization techniques. This role will be lab-based, driving projects forward through innovation. | 11/24/2025 |
| 142 | MilliporeSigma Jaffrey, NH Project Management Engineer Master of Science Degree in Plastics Engineering, Biomedical Engineering, or other Engineering discipline Exp: 1+ years |
Join our team as a Project Management Engineer, where you'll take the lead on exciting projects focused on validating new, repaired, and transferred injection molds. In this role, you will be responsible for building the justification, scope, and budget necessary to support investments in the fabrication or repair of injection molds and related equipment. Proactively maintain outsourced injection molds by providing guidance to suppliers and ensuring internal quality/supply standards are met. | 11/24/2025 |
| 143 | MilliporeSigma Lenexa, KS Process Engineer Bachelor’s degree in Chemical Engineering, Bioprocess Engineering, or related Engineering Discipline Exp: 1+ years |
Primary responsibility is to monitor and support the Dry Powder Manufacturing process in Lenexa, KS. It is a 24/7 media manufacturing plant which requires round the clock support. The position is responsible for understanding the Dry Powder Media manufacturing process to include blending, pin milling, dispensing/packaging, and the cleaning/drying of the equipment. The incumbent will navigate the process control systems for the equipment and understand how the system interfaces and stores data to OSI PI historian. The engineer will have knowledge of product powder attributes such as particle size, bulk density, flowability, and cohesiveness. The process engineer is the liaison between maintenance, engineering, and the shop floor. Provide support and mentoring to other engineering and engineering support personnel. Assist operations implementation of process improvements and during equipment startup and commissioning activities. | 11/24/2025 |
| 144 | MilliporeSigma St. Louis, MO Quality Assurance Product Release Analyst Bachelor’s Degree in a scientific (Biology, Chemistry, etc.) discipline Exp: 1+ years |
The Quality Assurance Product Release Analyst plays a role in ensuring the timely release of purchased and produced goods. This position is responsible for performing a variety of quality review functions according to established criteria and guaranteeing that products meet all necessary specifications. | 11/24/2025 |
| 145 | MilliporeSigma Bellefonte, PA Associate Production Scientist Bachelor’s degree in Chemistry, Biochemistry, Biology, Chemical Engineering or other Life Science field Exp: 1+ years |
MilliporeSigma in Bellefonte, PA is seeking an Associate Production Scientist. In this role you will manufacture or evaluate gas chromatographic (GC) capillary products according to established protocols, provide technical support to others, and perform operations in support of the group and department. | 11/24/2025 |
| 146 | MilliporeSigma Bedford, MA Scientist 1 - Chemistry Bachelor’s degree Exp: 6+ months |
MilliporeSigma in Bedford, MA is seeking a Scientist 1. The Scientist 1 within the Filtration Research and Development department will assist in the design, development, and testing of novel filtration products/technologies suitable for the manufacture of therapeutic biopharmaceuticals. | 11/24/2025 |
| 147 | MilliporeSigma Indianapolis, IN Microbiology Analyst 2 Bachelor’s Degree in Biology, Immunology, Biochemistry or other Science or Medical discipline Exp: 1+ years |
You will help ensure our manufacturing areas are meeting all pharmaceutical standards, including our aseptic environment. You will assist with collecting samples on critical utilities such as nitrogen, process air and the sites’ water systems. You will help with performing media fills including qualification and release in support of the environmental monitoring program. You will help with maintaining equipment and adhering to the sites Environmental Health and Safety program. You will assist with routine lab-related tasks and ensuring your work area is tidy to support audit readiness and bring issues to supervision immediately for escalations. You will also support QC in-process testing as a backup for weekend work. | 11/24/2025 |
| 148 | Modulo Bio San Diego, CA Stem Cell Scientist MS in Genetics, Molecular Biology, Developmental Biology, Biochemistry, Regenerative Medicine, Neuroscience, or related field Exp: 1+ years |
Modulo Bio is seeking a Stem Cell Scientist to develop and scale an induced-pluripotent stem cell (iPSC)-based in vitro model of the neuroimmune system. Modulo Bio is building a proprietary immune cell modeling platform, which incorporates human genetics, functional genomics, molecular biology, cellular and tissue profiling, disease model engineering, and advanced computational models. The successful candidate will build a complex cell model platform with the goal of improving our understanding of human biology and therapeutic interventions to inform early and late stage pipeline efforts. Candidates with an eagerness to work within a highly leveraged, team-driven, dynamic research environment will be prioritized. The candidate will work in close collaboration with our internal Computational Biology group which is focused on next-generation sequencing (NGS), functional genomics, cell or tissue profiling, and bioinformatics analyses of cutting-edge large-scale genetic screening or single-cell technologies to enhance our analytic capabilities and to reveal the underlying mechanisms of human disease. | 11/24/2025 |
| 149 | Moog Buffalo, NY Associate Product Engineer Bachelor of Science in Mechanical or Electrical Engineering, or comparable field of technology Exp: 0-2 years |
As an Associate Product Engineer, with Moog Aircraft Group’s Electronics Operations Engineering Team, you will be assigned direct engineering responsibility for a variety of production programs. Work assignments require some originality and unreviewed action. You will receive program and technical guidance from the department supervisory personnel, project, senior product, or product engineers. | 11/24/2025 |
| 150 | Moog Buffalo, NY Project Engineer, Test Equipment MS Degree in Engineering Exp: 1 year |
As a Project Engineer, Test Equipment in our Space & Defense Group in East Aurora, NY you will be responsible for design and development of hydraulic, electro-hydraulic, electro-mechanical, servo-mechanism, and electro-pneumatic components and systems that will be used to test the products of Moog, Inc. | 11/24/2025 |
| 151 | Moog Buffalo, NY Electronics Development Engineer BS degree in Electrical Engineering Exp: 1 year |
The Commercial Aircraft Electronics Group is looking for an Electronics Development Engineer to be responsible for the development and sustainment of Flight Control Computers (FCCs), Actuator Control Units (ACUs), and Motor Control Electronics (MCEs) for primary and secondary control systems for commercial aircraft. | 11/24/2025 |
| 152 | NAMSA Irvine, CA Laboratory Technician - Quality Control Bachelors degree Exp: 0 years |
Clean glassware and prepare reagents for use in laboratory testing. Perform routine disposal of laboratory waste including disposal of test articles. Assist with making solutions and preparing reagents. Assist in the preparation of items for testing. May be involved in various testing activities in accordance with SOPs, applicable work instructions. Review raw materials and final finished media for conformance with applicable material specifications and SOPs. May be responsible for extractions, test article and control preparation, animal holding and preparation and solution preparation. May be responsible for chain of custody, delivery of samples, filing and sample distribution/shipping. Accurately collect and record raw data in logbooks and on worksheets. Maintain clean workspace, testing supplies, and equipment. May be responsible for checking laboratory equipment, being on-call and responding to continuous monitoring alarms in accordance with criteria outlined in Standard Operating Procedures. May be required to operate specified laboratory equipment. Other duties as assigned. | 11/24/2025 |
| 153 | NAMSA Atlanta, GA Microbiology Technologist Bachelor's degree Exp: No exp |
May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. Accurately collects and records raw data in logbooks and on worksheets. May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. May be required to perform required specific testing as applicable. May be required to operate specified laboratory equipment. May perform Environmental Monitoring, clean and disinfect cleanroom suites (required as applicable). Other duties as assigned. | 11/24/2025 |
| 154 | Natera San Carlos, CA QC Reagent Associate I BS/BA degree in Biological Sciences, Biology, Chemistry or a related field Exp: 1+ years |
Support the activities for reagents used in the Operations Department’s Clinical Laboratories. Executes the preparation and qualification of molecular diagnostic reagents. Performs Quality Control tests on new incoming shipments of raw materials and small-scale manufacturing procedures (formulations and dispensing) reagent. Reviews data obtained for compliance to specifications and reports abnormalities. Maintains and improves QC documentation pertaining to raw material specification, reagent qualification, and QC testing. Support Incoming Quality Control activities as needed. | 11/24/2025 |
| 155 | Natera San Carlos, CA Lab Associate Bachelor’s degree in life-science or related field Exp: 1 year |
The Lab Associate supports R&D labs by ordering, receiving, and storing reagents and materials. Upkeeps laboratory consumables and reagents inventory. Fulfills various requests by research staff related to laboratory workflows and anticipate laboratory needs. | 11/24/2025 |
| 156 | Natera San Carlos, CA Research Associate 1 BS/BA in a biological science or equivalent Exp: 1-2 years |
The Research Associate 1 performs laboratory procedures of varying complexity contributing to cross functional activities as part of the Oncology Team, a multidisciplinary team within the research and development department. | 11/24/2025 |
| 157 | Neuropace Mountain View, CA Manufacturing Engineer BS degree in mechanical or manufacturing engineering Exp: 1-2 years |
We are currently seeking a Manufacturing Engineer to join our team at NeuroPace. The Manufacturing Engineer will support the development, documentation, verification, and ongoing manufacturing of products and processes required to produce an implantable Neuro-Stimulator and supporting lead systems. | 11/24/2025 |
| 158 | NewLimit South San Francisco, CA Vivarium Technician Bachelor’s degree (B.A./B.S) in animal or life sciences field Exp: 1 year |
NewLimit is seeking a Vivarium Technician with experience in rodent husbandry and in vivo technical procedures. In this role, you will help support vivarium operations, animal husbandry, and in vivo research in collaboration with New Limit’s product teams to test reprogramming medicines in pre-clinical rodent models. | 11/24/2025 |
| 159 | NextPhase Mansfield, MA Quality Engineer Bachelor’s Degree in Engineering, Quality Assurance or related Exp: 1+ year |
The Quality Engineer will support the Quality Management System (QMS) to ensure compliance to FDA Quality System Regulation, ISO 13485 and other relevant Quality System Standards. The Quality Engineer will also participate in product development teams to provide design control quality assurance support to medical device development and validation efforts. | 11/24/2025 |
| 160 | Nordson Duluth, GA Electrical Engineer I Bachelor’s degree in electrical engineering or computer engineering Exp: 0-3 years |
The Electrical Engineer drives continual improvement in product quality for Nordson. They serve as the primary engineering contact for our global field and sales teams. They are responsible for maintaining communication between the field, manufacturing, and product development engineering relative to customer concerns and quality issues. The EE owns the Corrective Action Request process and ensures a data driven approach is executed to yield qualified corrective actions. This position interfaces with sales, purchasing, factory assembly and planning teams, machine shop, external vendors, and other engineering organizations within Nordson. | 11/24/2025 |
| 161 | Nortech Bemidji, MN Quality Engineer Bachelor’s degree in engineering, quality, or closely related subject Exp: 1 year |
Work with manufacturing and engineering to ensure clear documentation, interpretation, and inclusion of customer requirements for assigned products. Support, plan, and implement activities concerned with development, application, and maintenance of quality standards for manufacturing processes, materials, products, and/or business systems. Develop, implement, and support standards and methods for inspection, testing, and evaluation relative to Nortech’s quality management standards to ensure products leaving the manufacturing or development organization are effective and free from defects or operational problems or errors. Review product, component, part, and assembly specifications, and develop and/or update testing-related documentation including test cases, plans, and flaw-reporting procedures. Work with training staff to ensure production and inspection personnel are properly trained. Support quality related issues such as interpretation of workmanship standards, manufacturing processes, customer prints, specifications and defect evaluations. Devise sampling procedures, design and develop forms and instructions for recording, evaluating, and reporting quality data. Develop and implement methods to ensure compliance of product development, documentation, manufacturing, and assembly processes. Maintain applicable quality records and perform quality audits in accordance with established standards. Compile, calculate, maintain, and report summary statistics required by customers. Inform product conformance decisions based on interpretation of quality data reports, SPC charts, and other applicable data; promptly notify management of concerns with potential to impact product volume, manufacturing lines, costs, or customer outcomes. Work with suppliers, customers, and internal departments on obtaining and/or responding to deficiencies and/or corrective actions. Coordinate the successful closure of closed loop corrective actions concerning quality issues of products and processes. Keep supervisor informed about project status, workload, concerns, questions, and progress. Demonstrate and support Nortech’s Mission, Core Values, policies and procedures at all times. May perform other duties and responsibilities as assigned. | 11/24/2025 |
| 162 | GRAM Grand Rapids, MI QC Microbiology Technician Bachelor’s degree in Microbiology or a related field Exp: 0-2 years |
The QC Microbiology Technician supports quality control and assurance by assisting the microbiology department with environmental monitoring, water testing, and client specific testing. The hours for this role are Fri-Sun, 6:00 am-6:00 pm. | 11/18/2025 |
| 163 | Flagship Labs Cambridge, MA Research Associate, Protein Degradation Master’s degree in Biochemistry, Cell Biology, Molecular Biology, or a related discipline Exp: 0+ years |
We are seeking a highly creative, resourceful, and motivated Research associate to join our Protein degradation team. The ideal candidate will help us set up our in-house protein production capabilities and support our cell-culture and molecular biology efforts. Strong candidates will be independent, goal-oriented, and have excellent communication skills. We are seeking individuals who can be highly adaptable and comfortable working in a dynamic and fast-paced collaborative and multidisciplinary environment. This is a unique opportunity to drive the growth of an early-stage biotechnology company where you can meaningfully define the next frontier of protein homeostasis modulators. The successful candidate will play a key role in driving our discovery efforts aimed at developing therapeutic strategies that modulate protein homeostasis. | 11/18/2025 |
| 164 | Flagship Labs Cambridge, MA Senior Research Associate, Analytical Development M.S. in Analytical Chemistry, Chemistry, Biochemistry, Chemical Engineering, or related field Exp: 1+ years |
We are searching for an experienced and enthusiastic Senior Research Associate (SRA) to contribute to the method development and characterization of novel nucleic acid therapeutics. We are looking for an individual who enjoys hands-on laboratory benchwork and brings scientific rigor and intellectual curiosity to their role. This individual will have the opportunity to work in a dynamic and fast-paced entrepreneurial environment as part of a highly collaborative and rapidly growing team. | 11/18/2025 |
| 165 | Helix San Diego, CA Lab Aide Bachelor’s degree in laboratory science or medical laboratory technology Exp: 0-1 years |
Join Helix's world-class, high-volume CAP/CLIA certified laboratory where transforming health organizations by weaving genomics into the fabric of healthcare. As a Lab Aide, you'll be at the forefront of our pre-analytical operations, working with a dynamic team that processes thousands of patient specimens daily. This role offers unique opportunities to challenge industry standards through innovative solutions. You'll gain hands-on clinical laboratory experience in a state-of-the-art facility while supporting the accessioning activities, plating procedures, and biohazardous waste program. With clear advancement pathways, you'll have the opportunity to grow from executing foundational tasks to becoming a subject matter expert and leader within the laboratory operations team. | 11/18/2025 |
| 166 | HighRes Biosolutions Beverly, MA Field Service Engineer I Bachelor’s degree in electromechanical/life science/engineering Exp: 0-3 years |
The Field Service Engineer position at HighRes Biosolutions is the primary role responsible for installation, maintenance, troubleshooting and repair of systems and devices at customer sites. This position is specialized on the hardware aspect of the products, coordinating with the Automation Support Engineer role in Customer Support and collaborating with the manufacturing and commissioning department (software and configuration-focused) for full coverage support of the products. Levels I and Junior are roles for carrying out Field Service Engineer responsibilities in either learning or assisted modes, with oversight and assistance from a team lead, supervisor, manager, or skilled technical Customer Service colleague(s). | 11/18/2025 |
| 167 | Hologic Newark, DE Senior Electrical Engineer Master’s degree in Electrical Engineering or related technical field Exp: 1-3 years |
As a Senior Electrical Engineer, you will design, develop, and evaluate electrical components and processes for our innovative breast and skeletal health products. You’ll be responsible for the physical layout of printed circuit boards, translating electronic schematics into reliable, manufacturable board designs, and ensuring compliance with performance and regulatory standards. | 11/18/2025 |
| 168 | Hologic Newark, DE Senior Quality Assurance Engineer Master's Degree in Electrical Engineering Exp: 1-3 years |
Are you a quality-focused professional passionate about ensuring excellence in manufacturing and production processes? Join Hologic as a Senior Quality Assurance Engineer and play a critical role in designing, implementing, and maintaining quality assurance protocols that meet internal and external regulatory standards for worldwide distribution. In this role, you’ll collaborate with cross-functional teams, lead quality initiatives, and drive continuous improvement to ensure the delivery of high-quality, innovative products that improve lives globally | 11/18/2025 |
| 169 | Hologic Newark, DE Quality Assurance Engineer Bachelor’s Degree Exp: 0-2 years |
Are you passionate about ensuring the safety, reliability, and compliance of life-saving medical devices? At Hologic, we are seeking a Quality Engineer to support the design, manufacturing, and quality assurance of medical devices. In this role, you will apply quality protocols, perform inspections, investigate non-conformances, and drive continuous improvement initiatives to uphold our commitment to excellence. If you’re detail-oriented, eager to learn, and ready to contribute to a team focused on delivering high-quality products, we encourage you to apply and be part of our mission to improve lives worldwide. | 11/18/2025 |
| 170 | Hologic Newark, DE Electrical Engineer 2 Bachelor’s or Master's Degree Exp: 0-2 years |
The Electrical Engineer designs, develops, modifies and evaluates components and processes used in the generation, manipulation, transmission and storage of electricity. Determines design approaches and parameters. Analyzes equipment to establish operating data, conducts experimental tests and evaluates results. Selects components and equipment based on analysis of specifications and reliability. Completes documentation and procedures for installation and maintenance. May interact with users to define system requirements and/or necessary modifications. Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors. Demonstrates good judgment in selecting methods and techniques for obtaining solutions. Networks with senior internal and external personnel in own area of expertise. A seasoned, experienced professional with a full understanding of area of specialization; resolves a wide range of issues in creative ways. This job is a fully qualified, career-oriented, journey-level position. Normally receives little instruction on day-to-day work, general instructions on new assignments. | 11/18/2025 |
| 171 | Hologic Newark, DE Electrical Engineer 3 Bachelor’s or Master's Degree Exp: 0-3 years |
The Electrical Engineer designs, develops, modifies and evaluates components and processes used in the generation, manipulation, transmission and storage of electricity. Determines design approaches and parameters. Analyzes equipment to establish operating data, conducts experimental tests and evaluates results. Selects components and equipment based on analysis of specifications and reliability. Completes documentation and procedures for installation and maintenance. May interact with users to define system requirements and/or necessary modifications. Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors. Demonstrates good judgment in selecting methods and techniques for obtaining solutions. Networks with senior internal and external personnel in own area of expertise. A seasoned, experienced professional with a full understanding of area of specialization; resolves a wide range of issues in creative ways. This job is a fully qualified, career-oriented, journey-level position. Normally receives little instruction on day-to-day work, general instructions on new assignments. | 11/18/2025 |
| 172 | Hologic San Diego, CA Scientist 2 - Post-Market Investigations Master’s in Chemistry, Biochemistry, Molecular Biology, Biomedical Engineering, or related scientific discipline Exp: 1-3 years |
We are hiring a highly motivated Scientist 2 in our Diagnostic division, Quality Technical Investigations (QTI) team. In this role and under QA function, you will coordinate and lead high complexity investigations related to customer complaints for assay reagents in Hologic's quality management system and moderate/high complexity projects in support of compliance and overall Hologic continuous improvement efforts. The incumbent will provide Technical Subject Matter Expertise (SME) to all levels of staff including QTI team as well as advising leadership as required. You may be responsible for communicating complex information to the key stake holders for effective decision making. When needed you may be responsible for performing laboratory hands on work to support QTI team’s projects, tasks etc. | 11/18/2025 |
| 173 | Hyperfine Guilford, CT Regulatory Affairs Associate Bachelor’s degree in a scientific or regulatory discipline Exp: 1 year |
As our Regulatory Affairs Associate, you will be an individual contributor responsible for analysis, evaluation, preparation, and submission of documentation for regulatory approval, ensuring Hyperfine products and procedures comply with US and global regulatory specifications. You will support our Regulatory team across different program areas, and will work on multiple projects concurrently. | 11/18/2025 |
| 174 | INCOG BioPharma Fishers, IN Filling Prep Specialist BS in biological sciences/biotechnology or related field Exp: 1 year |
The Filling Prep Specialist’s primary responsibility is to efficiently and safely set up and operate the various pieces of production equipment within the facility. They will be expected to work hands-on, be actively involved in continuous process improvements while taking ownership of the quality and quantity of product produced. The ideal candidate should possess a strong mechanical aptitude with strong trouble shooting skills on manufacturing equipment. They should demonstrate mentor and leadership skills to motivate manufacturing personnel, drive timely production activities and inspire problem solving & solution driven thinking. | 11/18/2025 |
| 175 | INCOG BioPharma Fishers, IN Formulation Specialist BS in biological sciences/ biotechnology Exp: 1+ years |
The primary responsibility of the Manufacturing Specialist in Formulation is to weigh/dispense, setup/operate equipment to produce the bulk drug product for sterile manufacturing. They will be expected to work hands-on, be actively involved in continuous process improvements while taking ownership of the quality and quantity of product produced. The ideal candidate should demonstrate mentor and leadership skills to motivate manufacturing personnel, drive timely production activities and work effectively with internal partners, clients, and vendors. | 11/18/2025 |
| 176 | INCOG BioPharma Fishers, IN Manufacturing Specialist BS in biological sciences/biotechnology or related field Exp: 1 year |
The primary responsibility of the Manufacturing Specialist in Formulation is to weigh/dispense, setup/operate equipment to produce the bulk drug product for sterile manufacturing. They will be expected to work hands-on, be actively involved in continuous process improvements while taking ownership of the quality and quantity of product produced. The ideal candidate should demonstrate mentor and leadership skills to motivate manufacturing personnel, drive timely production activities and work effectively with internal partners, clients, and vendors. | 11/18/2025 |
| 177 | INCOG BioPharma Fishers, IN Tech Transfer Engineer Bachelors’ or Masters' degree in Science or Engineering Exp: 1-3 years |
The Technical Services and Manufacturing Sciences (TSMS) Technical Transfer Engineer will be responsible for supporting all facets of Tech transfer, Process Validation, GMP Floor Support, and Continued Process Verification in accordance with current good manufacturing (cGMP) for clinical and commercial programs. This role will provide strong technical oversight to the production to ensure robust and reliable production processes are established. | 11/18/2025 |
| 178 | INCOG BioPharma Fishers, IN TSMS Engineer Bachelors’ or Masters' degree in Science or Engineering Exp: 1-3 years |
The Technical Services and Manufacturing Sciences (TSMS) Technical Transfer Engineer will be responsible for supporting all facets of Tech transfer, Process Validation, GMP Floor Support, and Continued Process Verification in accordance with current good manufacturing (cGMP) for clinical and commercial programs. This role will provide strong technical oversight to the production to ensure robust and reliable production processes are established. | 11/18/2025 |
| 179 | INCOG BioPharma Fishers, IN TSMS Operations Engineer Bachelor's degree in Science or Engineering Exp: 1-2 years |
The Technical Services and Manufacturing Sciences (TSMS) Operations Engineer will provide direct technical support to manufacturing operations on the production floor in accordance with current good manufacturing practices (cGMP) for clinical and commercial programs. This role will work closely with manufacturing operators and supervisors to ensure smooth production operations, troubleshoot technical issues, and support process execution as specified. | 11/18/2025 |
| 180 | Indivior Raleigh, NC MQA Specialist - 2nd Shift Bachelor’s degree in science, engineering field Exp: 1 year |
The Manufacturing Quality Assurance (MQA) Specialist – 2nd Shift is responsible for providing quality oversight to all manufacturing areas to ensure product quality and SOP/GMP compliance. The MQA Specialist will work closely with production personnel to complete in-process batch record review, resolve batch related issues, and ensure proper good documentation practices. In addition, the MQA Specialist will be responsible for performing routine environmental monitoring to assess the viable and nonviable particulate levels within classified manufacturing rooms and support rooms. | 11/18/2025 |
| 181 | Indivior Raleigh, NC Environmental Monitoring Technician Bachelor’s degree in Chemistry, Microbiology, Biology or other related Science Exp: 1 year |
The purpose of the EM Technician I is to perform routine environmental monitoring to assess the viable and nonviable particulate levels within classified manufacturing rooms and support rooms. | 11/18/2025 |
| 182 | Insmed San Diego, CA Senior Research Associate, Quality Control Master’s degree in relevant discipline Exp: 0 years |
We’re looking for a Senior Research Associate, Quality Control to help us expand what’s possible for patients with serious diseases. Reporting to the Associate Director, Quality Control, you’ll be involved in transfer of method from Analytical Development into QC. The Quality Control Senior Research Associate will author and execute phase appropriate qualification/validation protocols and reports of QC methods to support product release, stability, and characterization. The role will perform analytical and biochemical analysis on lot release, stability, and process characterization samples to support Insmed AAV Gene Therapy products. | 11/18/2025 |
| 183 | Integer Plymouth, MN Process Development Engineer I Bachelor’s degree in an engineering or related technical field Exp: 0-3 years |
The primary purpose of this position is to perform work which involves general engineering methods and tools. As an entry level engineer, you will ensure that Integer’s internal and external customer expectations are met or exceeded with the direction, instruction and guidance from more experienced engineers and managers in your organization. | 11/18/2025 |
| 184 | Integer Palm Harbor, FL Design Assurance Engineer I Bachelor’s degree in a related field Exp: 0-3 years |
The primary purpose of this position is to perform work which involves conventional engineering practice. Ensures Integer’s internal and external customer expectations are met or exceeded. Initiates, directs and manages the design, development, constructing and modification of products and processes from conception to implementation. Works closely with other departments to coordinate design engineering activities. Reviews, initiates or approves engineering drawings, layouts, changes orders and specifications | 11/18/2025 |
| 185 | Integer Plymouth, MN R&D Engineer I Bachelor’s degree in an engineering or related technical field Exp: 0-3 years |
The primary purpose of this position is to perform work which involves general engineering methods and tools. As an entry level engineer, you will ensure that Integer’s internal and external customer expectations are met or exceeded with the direction, instruction and guidance from more experienced engineers and managers in your organization. | 11/18/2025 |
| 186 | Integra LifeSciences Braintree, MA Quality Engineer II - Design & Reliability Assurance Master’s degree in science, Engineering (Biomedical or Mechanical) Exp: 0-2 years |
The Quality Design and Reliability Assurance (DRA) Engineer II is responsible for the efficient and compliant support of New Product Development (NPD) and Sustaining/Remediation project(s) of varying scope and complexity in the Tissue Technology (TT) division, specifically the Boston/ Braintree site. The role contributes and supports the design and development of new and improved products. The (DRA) Engineer II will interact with external design and development partners, participating on cross-functional project teams through all phases of the product development process, and assisting the technical team with planning, executing, documenting, and communicating testing activities. The role works with Product Development, Project Management, Regulatory, Marketing and Medical Affairs. | 11/18/2025 |
| 187 | Iovance Philadelphia, PA Process Development Associate I Bachelor’s degree (B.S./B.A.) in a life science or STEM-related discipline Exp: 1+ years |
The Process Development Associate I will provide process and analytical support to Tumor Infiltrating Lymphocyte (TIL) clinical and commercial development projects as part of the late-stage process development team. The successful candidate will have prior cell culture, process or method development, and cGLP/cGMP knowledge and experience. This role is a lab-based position, based in the Iovance Cell Therapy Center (iCTC) in Philadelphia, PA. | 11/18/2025 |
| 188 | Johnson & Johnson Danvers, MA Design Quality Engineer Bachelor’s degree in engineering or scientific discipline Exp: 1+ years |
The ideal candidate for the Design Quality Engineer position will support various New Product Development and sustaining activities as well as play a role in product risk management, cybersecurity, change controls, and design controls. This engineer should excel in an environment that embraces teamwork, change, risk-based decision-making and flexibility. Be ready to make a significant contribution to a dynamic, fun, multi-disciplinary team, where a self-motivated engineer with excellent written and verbal communication skills stands ready to succeed. | 11/18/2025 |
| 189 | Johnson & Johnson Raritan, NJ CAR-T Manufacturing Operator Bachelor’s degree required in Life Sciences or Engineering Exp: 0-2 years |
This position is responsible for performing manufacturing procedures and the execution of scheduled tasks within a CGMP environment. This position is responsible for the quality and maintaining the highest standards in compliance with company policies, procedures, and all applicable regulations. Responsible for fostering site pride and J&J citizenship. | 11/18/2025 |
| 190 | Jubilant HollisterStier Spokane, WA Process Engineer I Bachelor’s of Arts or Science with a major in Biology, Chemistry, Physics, or Engineering Exp: 0-5 years |
The Process Engineer I/II/IIIprovides ownership and focus for pharmaceutical processes and technical transfers at Jubilant HollisterStier. This position will engage in and manage projects and multi-disciplinary teams with direct supervision. The process engineer will also contribute technical direction for complex projects and exhibit clear communication skills with all levels of employees. | 11/18/2025 |
| 191 | KBI Durham, NC Manufacturing Associate I Bachelor's degree in a related scientific or engineering discipline Exp: 0-2 years |
The Manufacturing Associate I/II will perform Upstream or Downstream production activities for early and late-phase Cell Culture programs in a GMP environment. Responsibilities include executing tasks per SOPs, batch records, and GMP/GDP/GLP standards, ensuring compliance and accuracy. The role involves various unit operations such as media/buffer preparation, bioreactor operations, aseptic techniques, chromatography, ultrafiltration, and drug substance filling. Candidates must maintain process ownership, facility upkeep, and thorough documentation review to ensure compliance.The ideal candidate should have a basic understanding of cell culture, fermentation, or purification unit operations, with preference given to those experienced in single-use platform technology. Strong written and verbal communication skills are essential. The role requires an energetic, motivated, and dynamic individual who is highly organized and capable of maintaining efficiency and a positive demeanor in a fast-paced, multitasking environment | 11/18/2025 |
| 192 | KBI Durham, NC Microbiology Associate I/II Bachelor’s/Master’s degree in Microbiology, Biology or related technological field of science Exp: 0 years |
Testing and support for the Microbiology Laboratory in support of a Contract Manufacturing biotechnology facility and Process Development. Responsibilities includes laboratory support, program testing, reporting of results, execution of protocols. | 11/18/2025 |
| 193 | KBI Durham, NC Research Associate I Bachelor’s degree in chemistry, biochemistry or related area Exp: 0+ years |
Join a highly technical analytical team in a dynamic work environment where you will participate in contracted client analytical programs as a member of the Analytical Development (AD) Department. The individual in this position will be responsible for executing experimental protocols and performing data analysis in biopharmaceutical laboratories. | 11/18/2025 |
| 194 | KBI Durham, NC Research Associate II Master’s degree in chemistry, biochemistry or related area Exp: 0+ years |
Join a highly technical analytical team in a dynamic work environment where you will participate in contracted client analytical programs as a member of the Analytical, Formulation and Stability (AFS) Department. This role is responsible for executing experimental protocols and performing elementary data analysis in the analytical laboratories. | 11/18/2025 |
| 195 | KBI Louisville, CO Research Associate I Bachelor’s degree in a scientific discipline Exp: 0-2 years |
Join an analytical team in a dynamic work environment where you will participate in contracted client analytical programs as a member of the Rapid Analytics team. The individual in this position will support biophysical characterization studies of biopharmaceutical products through executing experimental protocols, performing data analysis, documenting work in technical reports, and presenting results to clients and management. Biophysical testing may include (but not limited to) SV-AUC, CD, DSC, FTIR, HPLC, UV-Vis. Required to work in teams to solve scientific problems, and to train and be trained by colleagues. | 11/18/2025 |
| 196 | KBI Boulder, CO Manufacturing Associate I Bachelor’s degree in a related scientific or engineering discipline Exp: 0-5 years |
Coordinate and perform cGMP manufacturing operations for manufacturing biopharmaceutical products. Ensure the effective use of material, equipment, and personnel while making products at high-quality levels. | 11/18/2025 |
| 197 | KBI Durham, NC Microbiology Associate II Master’s degree in a scientific discipline Exp: 1 year |
The Microbiology Associate II will be part of the Microbiology Department responsible for the testing and support for the Microbiology Laboratory in support of a Contract Manufacturing biotechnology facility and Process Development. The position will be a first shift, 10-hour/shift position, located at the Hamlin Road facility. Responsibilities include laboratory support, program testing, reporting of results, execution of protocols. | 11/18/2025 |
| 198 | Kestra Kirkland, WA Systems Engineer MS degree of Engineering Exp: 1 years |
The Systems Engineer will interact with customers, customer advocates, stakeholders, human factors and a variety of engineering disciplines to understand intended product uses, product concepts and technology. They are directly responsible for the development, review and ongoing maintenance of high quality, well understood, broadly communicated system and software requirements and are expected to develop expertise in these same areas. | 11/18/2025 |
| 199 | Krystal Biotech Pittsburgh, PA Process Validation Associate Bachelors’ Degree in Chemical Engineering, Biomedical Engineering, or related Exp: 1+ years |
Krystal Biotech is seeking a highly motivated Process Validation Associate (1+ years’ experience) or Engineer (3+ years’ experience) to support process validation planning, design, and execution. This person will be responsible for risk assessments, process improvements, investigations, and other projects. They will also play a pivotal role in technology transfer and ensuring processes transition properly from site to site. | 11/18/2025 |
| 200 | Krystal Biotech Pittsburgh, PA Bioprocess Engineer Bachelor’s degree, preferably in life sciences Exp: 1+ years |
Krystal Biotech, Inc is seeking a highly motivated and dynamic Bioprocess Engineer to support our product manufacturing at our Pittsburgh GMP facility. This role is critical to our make a meaningful difference in the lives of underserved patient populations having rare diseases. Quality, safety and on-time delivery is a must to be successful in this role! The ideal candidate will have foundational experience in upstream and/or downstream biologics or gene therapy manufacturing. | 11/18/2025 |
| 201 | LabConnect Cleveland, OH Laboratory Technician - Sample Processing Services Bachelor’s degree, preferably in life sciences Exp: 1 year |
The laboratory technician is responsible for sample processing and aliquoting. Process samples, including nucleic acid extractions, PBMC/BMMC isolations, plasma separation, specimen aliquoting, and other methods as required. Ensure sample integrity to meet client expectations. | 11/18/2025 |
| 202 | Eurofins Tustin, CA Asbestos PLM Analyst Bachelor’s degree in microbiology, biology, geology or a closely related science Exp: 1+ years |
The Analyst primarily performs analysis of bulk samples using PLM for asbestos. Analyst prepares and analyzes environmental samples according to scientific methodology in compliance with company Quality Assurance programs and SOP’s, and must be knowledgeable of both job-specific routine and complex analyses. The analyst validates and reviews data for accuracy, and enters laboratory data into the LIMS that ultimately generates required reports to clients. Schedules sample workload according to due dates and sample hold times, and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation. | 11/09/2025 |
| 203 | Eurofins Malvern, PA Characterization Scientist MS in Biochemistry, Chemistry, or related field Exp: 0-2 years |
Perform routine biochemical analyses for characterization of monoclonal antibodies in support of pharmaceutical development, including peptide mapping, A280, LCMS, size exclusion chromatography, fraction collection, or other routine methods. Sample preparation, distribution, and data collection, understanding of how to process data from chromatograms is a must. Reporting of data in accordance with requirements set forth by the department. Ensure maintenance of detailed documentation of assay development and qualification | 11/09/2025 |
| 204 | Eurofins Cedar Falls, IA Quality Assurance Assistant BS or BA in chemistry or related field Exp: 1-2 years |
The Quality Assurance Assistant assists the Quality Assurance (QA) Manager during audits and client visits. Helps maintain reference data in LIMS and performs spot audits internally at the request of the QA Manager. Performs customer service requests for Project Management staff, supplies SOP's, certification information, and method information. Works with the laboratory to maintain SOP's and other method performance documentation as directed by the QA Manager. | 11/09/2025 |
| 205 | Eurofins St. Charles, MO Associate Scientist I B.A. or B.S. Degree Exp: 6 months |
Eurofins Discovery provides lab research services for pharmaceutical and biotech organizations in a wide range of therapeutic areas to promote novel therapies for patients in need. This role will conduct industry leading cell-based and analytical assays in a laboratory setting with automated and classical methods. | 11/09/2025 |
| 206 | Eurofins Lancaster, PA Scientist - Data Review Bachelor’s degree in molecular/cellular biology or other related degree Exp: 1-2 years |
Ensure that the client receives high quality data and reports that adhere to client and good manufacturing process (GMP) requirements. Reviewing laboratory documentation for accuracy, consistency, and clarity. Gain a technical understanding of the techniques for the assays in which review is being performed. Begin to gain industry knowledge of the testing being completed within the department. Document work as required for GMP compliance | 11/09/2025 |
| 207 | Eurofins Cedar Falls, IA Quality Assurance Technician BS or BA in chemistry or related field Exp: 1-2 years |
The Quality Assurance Assistant assists the Quality Assurance (QA) Manager during audits and client visits. Helps maintain reference data in LIMS and performs spot audits internally at the request of the QA Manager. Performs customer service requests for Project Management staff, supplies SOP's, certification information, and method information. Works with the laboratory to maintain SOP's and other method performance documentation as directed by the QA Manager. | 11/09/2025 |
| 208 | Eurofins Rensselaer, NY QC Sampling Team Lead – Raw Materials Bachelor’s degree in Life Sciences or related field Exp: 1+ years |
As the QC Sampling Team Lead – Raw Materials, you will oversee a team responsible for sampling and inspecting raw materials used in biopharmaceutical manufacturing. You’ll ensure compliance with GMP standards, coordinate daily operations, and support team development while maintaining a strong presence in cleanroom environments. | 11/09/2025 |
| 209 | Evonik Birmingham, AL Microbiology Lab Technician Bachelor’s degree in microbiology, biological sciences, or related field Exp: 1 year |
This position is responsible for conducting routine microbiological testing, documentation, and data analysis, of utilities, raw materials, facilities and equipment. Additionally, the microbiology technician will be responsible for upkeep of the laboratory, laboratory supplies, and other various routine laboratory tasks. | 11/09/2025 |
| 210 | Evonik Lafayette, IN Facilities Plant Engineer Bachelor's degree in engineering (Civil, Structural, Architectural, Industrial, or Mechanical) Exp: 1-2 years |
The Plant Engineer oversees maintenance activities and small capital projects within assigned areas, providing independent engineering support to ensure safe, efficient, and compliant operations. The role defines, plans, and executes cost-effective projects in line with engineering standards, regulations, cGMP, and Evonik policies. The Plant Engineer drives continuous improvement to reduce costs and maintain high-quality, reliable operations, and may also lead medium-scale capital projects or support new product cost estimates. | 11/09/2025 |
| 211 | Evonik Birmingham, AL Validation and Qualification Specialist Bachelor’s degree preferably in Science or Engineering discipline Exp: 1-3 years |
Support existing qualification and Validation programs. Adhere to quality and regulatory compliance policies in support of GMP operations efforts. | 11/09/2025 |
| 212 | Evotec Redmond, WA Senior Associate Scientist, Purification Process Design BS or MS degree in Engineering, Biochemistry or related field Exp: 0-4 years |
We’re looking for a passionate and curious Senior Associate Scientist to join our team. If you’re excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you’ll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories. As a Senior Associate Scientist at Just-Evotec, you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It’s a role where your curiosity will fuel both your personal growth and the success of the team. | 11/09/2025 |
| 213 | Exact Sciences Phoenix, AZ Quality Control Associate I Bachelor’s degree in Clinical Laboratory Science or Medical Technology or in the chemical or biological sciences Exp: 1+ years |
The Clinical Laboratory Quality Control (QC) Associate (Tues - Sat and Sun - Thurs 10:00am - 6:30pm) performs and functions within the Technical Laboratory under the guided direction of the Supervisor, Clinical Laboratory Quality Control Lead, or designee. In this support position, the Clinical Laboratory QC Associate ensures daily QC operations are effective and efficient by coordinating with leadership to anticipate and resolve issues related to efficiencies in quality control, and laboratory processes. | 11/09/2025 |
| 214 | Fresenius Kabi Melrose Park, IL Validation Engineer Bachelor’s degree in a Science or Engineering field Exp: 1 year |
Responsible for providing technical support to operations in terms of equipment/system/process initial validation and equipment/system/process requalifications. Will participate in process and equipment improvement teams charged with enhancing the compliance and performance of plant systems, while considering the regulatory requirements for change control. The individual must become certified to enter Controlled Areas of the plant (class 100, 10,000 and 100,000). The ability to write reports clearly, concisely and accurately; accurately record data and a basic understanding of statistical analysis is also required to perform these duties. Weekends and Off-shift hours are periodically required. | 11/09/2025 |
| 215 | Fresenius Kabi Warrendale, PA Quality Engineer B.S. degree in Engineering (Mechanical, Electrical, Biomedical preferred) Exp: 0-3 years |
This position will analyze and execute processes to ensure product quality in the Production Unit (PU). This position will support core quality system processes to ensure compliance with applicable medical device regulations and standards (FDA, EU, Health Canada, ISO 13485) by providing operations assistance, tracking quality metrics, reviewing and approving quality system records, and analyzing data. Requires working in a cross-functional team environment. Applies engineering principles to resolve difficult problems. | 11/09/2025 |
| 216 | FUJIFILM Biotechnologies College Station, TX QA Analyst III Master’s Degree Exp: 1+ years |
The Quality Assurance (QA) Analyst III, under minimal direction, will be responsible for review and/or approval of basic and technical documentation, drafting and reviewing of internal Quality policies and procedures, performing product related activities, performing Quality audit functions, performing product release activities, identifying process and Quality System improvements, and acting as a QA liaison internally and externally. | 11/09/2025 |
| 217 | FUJIFILM Biotechnologies Mesa, AZ Development Lab Chemist Bachelor’s degree in chemistry or material science Exp: 1-5 years |
Responsibilities include supporting pilot line builds for formulated products, executing formulated products build plans, generating test data, assisting maintaining lab and pilot line equipment including 4-point probe, ellipsometer, FTIR, back up SEM/FIB and XRR operator, general lab assistance where needed. | 11/09/2025 |
| 218 | FUJIFILM Biotechnologies Mesa, AZ QC Chemist BA/BS in Chemistry or related degree such as Biochemistry, Biology, Physics or Mathematics. Exp: 0-1 years |
The QC Chemist serves as a Quality Control Specialist responsible for analyzing semiconductor materials in support of product qualification and to support all Quality Control laboratory processes. | 11/09/2025 |
| 219 | FUJIFILM Biotechnologies Research Triangle Park, NC Production Technician 3 Downstream Bachelor’s degree in life science, engineering, or relevant technical field Exp: No exp |
The Production Technician 3 executes manufacturing processing steps and associated activities while maintaining strict adherence to Current Good Manufacturing Practice (CGMP) quality and regulatory standards. Flexibility with working hours and shift rotation is essential to effectively support the 24/7 manufacturing facility. | 11/09/2025 |
| 220 | FUJIFILM Biotechnologies Holly Springs, NC Engineer / Scientist 2 Master’s degree Exp: No exp |
The Engineer/Scientist 2 will provide technology transfer support and technical oversight during manufacturing operations | 11/09/2025 |
| 221 | FUJIFILM Biotechnologies Holly Springs, NC Manufacturing Support Associate 1 BA/BS in life sciences Exp: No exp |
The Manufacturing Support Associate performs manufacturing support activities to ensure compliant and reliable production. This manufacturing facility is 24/7 operational and the role may require to be flexible with working hours. | 11/09/2025 |
| 222 | FUJIFILM Biotechnologies Research Triangle Park, NC Associate 1, Quality Control Microbiology Bachelor’s degree in Life Science or Biology Exp: No exp |
The Associate 1, Quality Control (QC) Microbiology is an entry level position responsible for performing routine microbiological testing of clean utility, environmental monitoring, and manufacturing batch samples. This role performs routine laboratory testing and support activities and participates in continuous improvement initiatives. | 11/09/2025 |
| 223 | Genentech South San Francisco, CA Scientist 2, Cell Culture, Protein Sciences Master’s degree in the Biological Sciences Exp: 1-3 years |
The departments of BioMolecular Research and Structural Biology, within the Protein Sciences Organization at Genentech are looking for a versatile, dynamic, and independent individual to contribute towards medium to large scale mammalian recombinant protein expression. In this collaborative role, the successful candidate will have the opportunity to work with other scientists and group leaders within and outside our department, driving projects autonomously to fulfill both straightforward and challenging protein production needs. | 11/09/2025 |
| 224 | Genentech Hillsboro, OR Automation Engineer BS degree in Engineering Exp: 0-2 years |
As a Frontline Automation Engineer, each day is a unique symphony of challenges and triumphs. Your role is pivotal in ensuring the timely delivery of life-saving medicines, making a tangible difference in the world. Every task you undertake, no matter how small, contributes to a larger purpose - the well-being of our patients. So, join our team in making a difference to Roche/Genentech and to our patients. You will be a member of the Frontline Automation Engineering Team which plays a key role in the support of our site’s make, assess, and release process. The individual selected into this role will provide frontline support and work collaboratively with maintenance, engineering, utilities, reliability teams, and end users to diagnose and troubleshoot equipment and processes. Additionally, you will work on project teams to deliver new capabilities and improve existing processes. The selected candidate will demonstrate a continuous improvement mindset and possess strong hands-on troubleshooting skills within a GMP environment. | 11/09/2025 |
| 225 | Genentech Hillsboro, OR Manufacturing Engineer B.S or higher in Mechanical Engineering, Electrical Engineering, Chemical Engineering, Biomedical Engineering, or related discipline Exp: 0-2 years |
As a Manufacturing Engineer at the Hillsboro Technical Operations Fill Finish facility, you will be responsible for supporting the design, operation, control and optimization of manufacturing equipment at HTO. The position serves as an equipment, process, or automation owner and is engaged in development, qualification, data analysis, troubleshooting, and continuous improvement activities. The Manufacturing Engineer plays a key role in day-to-day operations, as well as design and delivery of local and major capital projects, and interacts with a cross-functional team to deliver on business objectives. | 11/09/2025 |
| 226 | Genezen Lexington, MA Analyst I, QC Raw Materials BS in Chemistry or other related science Exp: 1-3 years |
The Quality Control (QC) Raw Materials Analyst is responsible for ensuring the quality of raw materials are suitable for the intended use by the Manufacturing Department. These activities are performed in accordance with cGMP, USP, EP, and JP guidelines as well as company policies and procedures. The QC Raw Materials Analyst I will support the day-to-day operations which include sampling, internal and external testing, controlling and releasing raw materials, as well as support QMS (Deviations, CAPA, Lab Investigations (OOS, AR, OOT), Documentation (SOPs/Forms/Material Specification), laboratory operational processes and Training. Supports method validation/verification activities for onboarding new raw materials, as well as internal/external audits. | 11/09/2025 |
| 227 | Genezen Lexington, MA QC Lab Support (Contractor) BA or BS in Life Sciences Exp: 1-3 years |
The QC Lab Support Contractor plays a critical role in supporting day-to-day quality operations within the cGMP QC laboratories. This role is responsible for overseeing all aspects of GMP lab supply management, documentation and record keeping, lab equipment maintenance, reagent preparation and general lab support. In addition, individual will ensure compliance with documentation practices and contribute to maintaining an organized and efficient laboratory environment. This position is based at our state-of-the-art facility in Lexington, MA. | 11/09/2025 |
| 228 | Genezen Lexington, MA Process Engineer I, Manufacturing Sciences & Technology Bachelor's or Master's Degree in Engineering or other related scientific discipline. Exp: 0-3 years |
The Manufacturing Sciences & Technology (MSAT) group plays a critical role in successful manufacturing of clinical and commercial products. The person in this role assists the MSAT team in the transfer of technologies, process validation and cGMP manufacturing of Genezen’s gene therapy products. This individual will contribute as a core member of various cross-functional teams, and interacts extensively with other departments within Genezen including Process Development, Manufacturing, Engineering, Quality, and Regulatory Affair etc. | 11/09/2025 |
| 229 | Genezen Lexington, MA QC Technician - Microbiology (Contract) Bachelor's degree in Microbiology or other related science Exp: 0-2 years |
The QC Technician contract role will be responsible for routine and non-routine QC sampling and testing for the quality of products manufactured for our clients. QC is responsible for execution of the Environmental Monitoring (EM) program in place to monitor Genezen's controlled manufacturing environments (cleanrooms) as well as monitoring of utility systems including Water for Injection (WFI), Pure Steam, Purified Water, Compressed Air and Gas systems. These activities are all performed in accordance with cGMP guidelines and are supported by departmental and interdepartmental policies and standard operating procedures (SOPs). This position is based at Genezen’s state-of-the-art facility in Lexington, MA. This role supports daily operations as well as occasional weekend and holiday operations. | 11/09/2025 |
| 230 | GenScript Pennington, NJ Associate Scientist, Quality Control Bachelor’s degree in Molecular Biology, Biochemistry, Microbiology or related scientific field Exp: 1-2 years |
The position reports to the Sr. QC Manager, is ideally suited for a professional with extensive technical knowledge, and a proven track record of developing and carrying out processes, that are suitable for use in GMP manufacturing of a wide range of clinical trial materials, and participating in the technology transfer. There is a great opportunity to lead and evolve this function within a CDMO business, to support a broad portfolio and advance the manufacturing capabilities to deliver products to the client projects that transform the lives of patients. | 11/09/2025 |
| 231 | GenScript Pennington, NJ (Sr). Scientist, Downstream Process Development Master’s in Chemical/Biochemical Engineering, Biological Sciences, or a related scientific discipline Exp: 1-3 years |
The position reports to the Associate Director, Downstream Viral Vector Process Development & MSAT Department. This role is ideally suited for a dynamic bench-focused individual to support/lead translation of research process to GMP-compliant manufacturing, and will develop, scale-up, and evaluate the technology transfer of viral vector processes. This is a great opportunity to join a fast-paced company, develop, and expand technical expertise to lead by example and potentially lead a small team in the near future. | 11/09/2025 |
| 232 | GenScript Pennington, NJ (Sr). Scientist, Upstream Process Development Master’s degree in Biology, Biochemistry, Chemical Engineering or equivalent Exp: 0-3 years |
The Scientist, Upstream Process Development & MSAT Department. reports to the Senior Manager, Upstream Viral Vector Process Development & MSAT Department. This role is ideally suited for a dynamic, bench-focused individual to support and lead the translation of research processes to GMP-compliant manufacturing. The successful candidate will develop, scale-up, and evaluate the technology transfer of viral vector processes in a fast-paced biotechnology environment. | 11/09/2025 |
| 233 | Getinge Wayne, NJ Engineer II, Mechanical MS in engineering discipline, mechanical preferred Exp: 1 year |
Effectively design, develop, and document medical devices and medical equipment that satisfy internal and external customer needs and business objectives. | 11/09/2025 |
| 234 | Gilead Foster City, CA Senior Research Associate, Formulation Process Development M.S in Pharmaceutical Science, Chemistry, Biochemistry, Chemical Engineering, or related scientific fields Exp: 0+ years |
Plan and successfully execute experiments and activities to support formulation and drug product process development. With general guidance, operate scientific equipment and tools such as HPLCs, UV-Vis, CE-SDS, and iCIEF to ensure applicable methods and techniques are followed. Clearly, timely, and accurately document data in appropriate repositories such as lab notebooks, reports, and protocols. Analyze, interpret, draw conclusions, and present or share data from executed experiments, including preparing appropriate documents such as reports and memos. Fully embrace a lean-agile mindset, a matrix working environment, and continuous improvement. Help support key project or department stakeholders as needed to ensure company objectives are met. Use established data, reports, and previous results to identify inappropriate variances and concerns, as well as identify and report inconsistent results to the manager or supervisor. Participate in group meetings and efforts by presenting data or preparing information for others to present. Support team initiatives to drive business process excellence, scientific innovation, and laboratory and work safety. | 11/09/2025 |
| 235 | Gilead Foster City, CA Sr Research Associate, Medicinal Chemistry Masters degree Exp: 0+ years |
As a Sr. Research Associate, you will participate a multi-disciplinary drug discovery team through the design and synthesis of new molecules. The successful candidate will have an excellent track record and a commitment to tackling drug discovery challenges through organic synthesis. | 11/09/2025 |
| 236 | Gilead Foster City, CA Research Associate, Medicinal Chemistry Bachelors degree Exp: 0+ years |
As a Research Associate, you will participate on a multi-disciplinary drug discovery team through the design and synthesis of new molecules. The successful candidate will have an excellent track record and a commitment to tackling drug discovery challenges through organic synthesis. | 11/09/2025 |
| 237 | Gilead La Verne, CA EH&S Specialist I MA/MS degree Exp: 0+ years |
An opportunity is available in the EH&S team at Gilead in La Verne, California. The successful candidate will be joining a highly motivated and cross functional team to help develop and elevate a proactive EH&S culture across our La Verne campus via administration of compliance related to our Sustainability and Injury and Illness prevention programs. You will use effective time management skills to work with limited supervision on routine projects to moderate complexity, including updating existing programs, protocols, and procedures. The Specialist will possess excellent communication and customer service skills and will be expected to maintain regular interaction with customer groups. | 11/09/2025 |
| 238 | Globus Medical Audubon, PA Project Engineer Bachelor's Degree in Mechanical Engineering, Bioengineering, Biomedical Engineering, or a similar field Exp: 0-3 years |
At Globus Medical, we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team is inspired by the needs of these patients, and the surgeons and healthcare providers who treat them. We embrace a culture of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions. Our solutions improve the techniques and outcomes of surgery so patients can resume their lives as quickly as possible. | 11/09/2025 |
| 239 | Globus Medical Audubon, PA Associate Quality Engineer Bachelor’s Degree required (science or engineering preferred) Exp: 0-2 years |
The Associate Quality Engineer will be responsible for achieving the highest quality level of manufacturing quality and quality system performance while ensuring compliance with all company policies and procedures and maintaining compliance with US FDA and international medical device regulations and ISO 13485 quality system requirements. As a contributor to the quality engineering organization, this professional will be a self-motivated and characterized as an excellent problem solver. This person will play an integral role in maintaining | 11/09/2025 |
| 240 | Globus Medical San Diego, CA Electrical Engineer B.S. degree in Electrical Engineering Exp: 1-3 years |
Our rapidly growing medical robotics division is searching for an enthusiastic electrical engineer wanting to make a difference. Our skillful engineers develop medical robots by working with top surgeons and cross-functional engineering teams. The Electrical Engineer will be part of the electrical engineering team responsible for designing and implementing electronic circuits for intra-operative neuromonitoring used within our surgical navigation and robotic products. The position will be hands-on with the individual capable of creative, novel, and systematic product development with minimum supervision. | 11/09/2025 |
| 241 | Globus Medical Audubon, PA Regulatory Associate Bachelor’s degree in health or science-related field, or equivalent; Engineering degree is a plus Exp: 0-2 years |
The Regulatory Affairs Associate assists in drafting, submitting and gaining clearance for 510(k) submissions, and approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products. This position entails development of FDA submissions, requiring working knowledge of products under review and of relevant regulations and guidance documents. This individual must be enthusiastic, positive, even-tempered and effective in building working relationships with internal teams while following FDA 21 CFR regulations. | 11/09/2025 |
| 242 | Cellares South San Francisco, CA Cell Therapy Manufacturing Specialist Bachelor’s Degree or diploma in a scientific or related field Exp: 1+ years |
We are seeking an innovative and highly motivated Cell Therapy Manufacturing Associate to join our Process Sciences team who will contribute significantly to the development and manufacture of our advanced cell therapy manufacturing platform. The primary focus of this position will be to support manufacturing operations, as well as day-to-day lab operations. This is a hands-on position that will train in Process Development, Analytical Development, and/or MSAT prior to joining the Manufacturing Group. Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows. | 11/03/2025 |
| 243 | Cellares Bridgewater, NJ Cell Therapy Manufacturing Specialist Bachelor’s Degree or diploma in a scientific or related field Exp: 1+ years |
We are seeking an innovative and highly motivated Cell Therapy Manufacturing Specialist to join our Process Sciences team who will contribute significantly to the development and manufacture of our advanced cell therapy manufacturing platform. The primary focus of this position will be to support manufacturing operations, as well as day-to-day lab operations. Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows. | 11/03/2025 |
| 244 | Cellares South San Francisco, CA Senior Systems Engineer Masters degree in Engineering, Physics or Biotech Automation Exp: 1 year |
We are seeking an innovative and highly motivated Senior Systems Engineer who will make significant contributions to the development of our advanced cell therapy manufacturing platform. The ideal candidate will have demonstrated experience in biomedical-related instruments and consumables development, integration, and verification activities. As a Senior Systems Engineer, you are expected to readily learn and adapt to Cell Shuttle technologies, take ownership of various tasks, and successfully drive them to completion. In your daily work, you will provide in-depth analysis for system characterization and troubleshooting, and help guide important decisions for continuous improvement projects. | 11/03/2025 |
| 245 | Cellipont Bioservices Woodlands, TX Manufacturing I Bachelors Degree in Life Sciences Exp: 0-1+ years |
Cellipont Bioservices is growing, and we are looking for a Manufacturing Associate I who believe in the potential bridging client's discoveries to patient cures and who want to challenge the status quo and take Cellipont and its clients to the next level. The Manufacturing Associate I is an entry level role and will be responsible for assisting in the planning and timely execution of manufacturing operations for a cGMP-compliant state-of-the-art cell processing/clinical manufacturing facility with emphasis on primary cell isolation and cell culture in an aseptic processing environment. The Manufacturing Associate I is responsible for following the standard practices outlined for the operation of the facility in accordance with the regulatory requirements for the manufacture of materials for our clinical studies, clinical trials and products. | 11/03/2025 |
| 246 | Cellipont Bioservices Woodlands, TX QA Technician I, Operations Bachelor's Degree Exp: 0-1 years |
Cellipont Bioservices is growing, and we are looking for a QA Technician I, Operations who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The QA Technician I, Operations will be responsible for monitoring systems and procedures to ensure compliance where applicable. The QA Technician I, Operations is responsible for providing Quality Assurance support real-time for GMP Manufacturing of Cell Therapies. This individual will be responsible for providing QA on the Floor during manufacturing including observing critical processes, review executed GMP documentation, and supporting other QA functions as needed. | 11/03/2025 |
| 247 | Cellipont Bioservices Woodlands, TX QA Technician II, Operations Bachelor's Degree Exp: 1-2 years |
Cellipont Bioservices is growing, and we are looking for a QA Technician II, Operations who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The QA Technician II, Operations will be responsible for monitoring systems and procedures to ensure compliance where applicable. The QA Technician II, Operations is responsible to provide Quality Assurance support real-time for GMP Manufacturing of master/working cell banks. This individual will be responsible for providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. | 11/03/2025 |
| 248 | Cellipont Bioservices Woodlands, TX QC Analyst I, Analytical Bachelors Degree preferred in Life Sciences discipline Exp: -=1 years |
Cellipont Bioservices is growing, and we are looking for a QC Analyst I, Analytical who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The QC Analyst I, Analytical will work in a fast-paced environment supporting the quality control department of a CDMO for manufacturing of cell therapies. The QC Analyst I, Analytical will be responsible for routine testing, assay transfer and assay validation, QC document preparation and revision (SOPs/Protocols/Reports), as well as support for laboratory setup and maintenance. The QC Analyst I, Analytical, will also be responsible for ensuring all activities are executed timely and cost effectively to ensure customer and stakeholder satisfaction. This role will also require the individual to demonstrate a strong ability to work cross-functionally and possess strong leadership skills. | 11/03/2025 |
| 249 | Centrillion Palo Alto, CA Laboratory Technician B.A./B.S. in a molecular biology, genetics, or microbiology Exp: 6 months |
We are looking for a Laboratory Technician to join our R&D team in Palo Alto. The role is part of a small group that divides their focus between innovative new projects and product development. The ideal candidate will be extremely organized, familiar with basic laboratory techniques, and excited to learn and grow within the team. Technicians will divide their time between hands-on laboratory work, data analysis, and lab organization and maintenance. Candidates with knowledge and experience of PCR, library preparation, NGS sequencing or RNA seq will be given preference. | 11/03/2025 |
| 250 | Cepheid Lodi, CA Manufacturing Support Engineer Master’s degree of engineering related discipline Exp: 0-2 years |
The Manufacturing Support Engineer is responsible for supporting manufacturing operations with engineering expertise to ensure the successful transfer of new products from development to manufacturing, ensuring robust manufacturing processes at commercialization, conducting failure investigations of commercialized products, and supporting processes to ensure performance within expected parameters.. | 11/03/2025 |
| 251 | Champions Oncology Rockville, VD Research Associate I, Radiopharmacology BS or MS degree in radiochemistry, biochemistry, chemistry, chemical engineering, biomedical engineering, biology, or related sciences. Exp: 0-2 years |
Perform cross-functional laboratory assays with a focus on synthesis and purification of radiolabeled compounds and their characterization. Assist in the development and execution of novel assays including collecting and processing data. | 11/03/2025 |
| 252 | Charles River Reno, NV Quality Assurance Auditor I Bachelor’s degree (B.A./B.S.) Exp: 1-2 years |
The position is responsible for performing audits of basic records and reports and inspections of routine processes to assure compliance with applicable regulatory requirements, international standards, and corporate policies and procedures. This individual will review protocols for compliance with all pertinent government and international GLP regulations for studies conducted at the Test Facility that are basic and routine in study design. The Quality Assurance Auditor will also prepare and review Quality Assurance files prior to Sponsor site visits; ensure that QA audit files are archived. | 11/03/2025 |
| 253 | Charles River Mattawan, MI Senior Associate Scientist, Project Scientist – Large Molecule Bioanalysis Master’s degree Exp: 1-2 years |
The Immunology and Immunochemistry disciplines support large molecule drug development using ligand binding assays, such as enzyme-linked immunosorbent assay, to measure large molecules and their immune responses. The main types of assays include Pharmacokinetic assays to measure drug and Immunogenicity assay to measure anti-drug antibodies and neutralizing antibodies. Other assay types also performed are branched DNA and cell-based assays. An array of platforms are used to support these assays that include spectrophotometer, Meso Scale Discovery, Luminex and Gyrolab. Utilizing these platforms/assays, the teams are responsible for the method development, validation and routine sample analysis in both the regulated and non-regulated space of non-clinical and clinical studies. | 11/03/2025 |
| 254 | Charles River Ashland, OH Research Analyst I, Formulations Bachelor’s degree (B.A./B.S.) in a relevant field Exp: No exp |
A Research Anaylst I – Formulations will prepare basic to complex dosing material and samples for vehicles, solutions, suspensions, diets, and dispensations independently with some oversight. | 11/03/2025 |
| 255 | Charles River Spencerville, OH In Vivo Technician I Bachelor’s degree (B.A./B.S.) in a biological science Exp: No exp |
A Technician I is in training to perform and become proficient in on-boarding tasks, procedures, and cooperating in a team environment. The technician is learning basic tasks required to conduct a study, which may include collecting and recording data in the performance of studies. Responsible for handling and restraining animals, clinical observations, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. The technician is working under close supervision to gain proficiency | 11/03/2025 |
| 256 | Charles River Reno, NV Immunopathology Analyst I Bachelor’s degree (B.A. / B.S) in laboratory science or related discipline Exp: No exp |
Generate and record data with minimal supervision in the performance of studies. Responsible for handling and processing samples and performing accurate data collection and reporting. Perform laboratory tasks by various basic methods. | 11/03/2025 |
| 257 | Charles River Ashland, OH Research Analyst I (Chemist) – Immunology Bachelor’s degree (B.A/B.S.) in scientific field Exp: 0-2 years |
Perform laboratory tasks by various basic methods. Generate and record data with minimal supervision in the performance of studies. Responsible for handling and processing samples and performing accurate data collection and reporting. | 11/03/2025 |
| 258 | Charles River Mattawan, MI Associate Scientist – Discovery Immunoassays Master’s degree Exp: No exp |
The Immunology and Immunochemistry disciplines support large molecule drug development using ligand binding assays (LBA), such as enzyme-linked immunosorbent assay (ELISA), to measure large molecules and their immune responses. The main types of assays include Pharmacokinetic (PK) assays to measure drug and Immunogenicity assay to measure anti-drug antibodies (ADA) and neutralizing antibodies (NAb). Other assay types also performed are branched DNA (bDNA) and cell-based assays. An array of platforms are used to support these assays that include spectrophotometer, Meso Scale Discovery (MSD), Luminex and Gyrolab. Utilizing these platforms/assays, the teams are responsible for the method development, validation and routine sample analysis in both the regulated and non-regulated space of non-clinical and clinical studies. | 11/03/2025 |
| 259 | Cipla Hauppauge, NY QA Validation - DPI Bachelor's degree in scientific discipline (e.g., biology, chemistry, pharmacy) or a related field Exp: 1-2 years |
Responsible for the coordination of supportive equipment and process validation activities such as testing, calibration, scale-up, engineering and validation studies, and assurance that the necessary project documentation is complete, accurate and in compliance with cGMP regulations. | 11/03/2025 |
| 260 | CPC Hauppauge, NY Chemist; Quality Control Bachelor’s degree in a science related field Exp: 1-9 years |
The Chemist is responsible for and has experience in performing chemical analysis for one of the assigned QC laboratories (Raw Material, Finished Product, Microbiology, ICP, Technical Support) which is responsible for the analysis and disposition of commercial materials (raw materials, finished product release, stability, validation, investigation), and environmental samples, as assigned, and documenting results in accordance with SOPs. | 11/03/2025 |
| 261 | CooperSurgical Tucson, AZ Laboratory Services Quality Technician I Bachelor's degree in one of the biological, chemical, or physical sciences Exp: 1 year |
Quality Control Lab Technician I role at Cord Blood Registry (CBR) is responsible for analyzing and documenting test results from our cord blood and cord tissue processed samples, releasing raw materials, supporting the analytical and processing equipment maintenance program, conducting environmental monitoring, and providing a wide range of critical functions that support the cryogenic storage of our client's final product. This position is also responsible for providing our internal customers with technical expertise while maintaining the highest quality services possible. The Quality Control Lab Technician I directly supports manufacturing to ensure the Product Operations function is provided with adequate equipment and materials to support stem cell processing activities. At the Technician I level, the individual performs critical daily activities involving high complexity testing, equipment maintenance and troubleshooting, interfacing with service providers, reagent testing, executing quality control assays and environmental monitoring activities. The role is also involved with supporting and executing validations, verifications, and projects within the Quality Control department. | 11/03/2025 |
| 262 | Cardinal Health Mansfield, MA Regulatory Affairs Specialist Bachelors in related field Exp: 0-2 years |
Regulatory provides regulatory affairs and product development consulting services to enable pharmaceutical, medical and biotechnology companies to obtain regulatory approvals. This function applies subject matter expertise to provide services in technical writing and regulatory submissions as well as clinical research and manufacturing process consulting. Regulatory Affairs plans, coordinates and implement regulatory strategies for products that require government approval. This job family proactively identifies regulatory requirements and risks for products and develops plans for product development programs and regulatory submissions. | 11/03/2025 |
| 263 | Cardinal Health Phoenix, AZ Development Engineer (Nuclear) Bachelor’s degree in related field (Electrical, Mechanical or Computer Science) Exp: 0-2 years |
As a Development Engineer, you will play a hands-on role supporting the design, testing, and improvement of systems that produce and distribute radiopharmaceuticals across the U.S. The Development Engineer is responsible for specific tasks and overall objectives to meet and exceed team and personal goals while managing multiple projects under general guidance. This role also conceptualizes project paths quickly and accurately, is a problem solver, and addresses challenges strategically and efficiently. | 11/03/2025 |
| 264 | Cardinal Health , Specialist, Quality Assurance Bachelor's degree Exp: 1-3 years |
The Specialist, Quality Assurance executes quality programs, policies, and procedures in a particular area of specialty (such as recalls and customer complaints) in order to minimize risks and drive supply chain integrity. With basic knowledge of quality assurance concepts, the Specialist creates reports on quality metrics and trends in support of resolutions to quality issues and the development of standard operating procedures. The Specialist frequently seeks guidance from more experienced Senior Specialists or Principal Specialists and assists on more complex projects to develop advanced knowledge and technical capabilities. | 11/03/2025 |
| 265 | Cresilon Brooklyn, NY Production Technician I Bachelor's or Master's Degree Exp: 0+ years |
The Production Technician I is responsible for the aseptic manufacturing of Cresilon’s products for the animal health industry. The Production Technician II will be trained in clean room operations, aseptic techniques, and must demonstrate the ability to successfully pass gowning qualifications. The position involves operating simple and complex processing equipment, routine sanitization of cleanroom facilities, and manual cleaning of equipment. The ideal candidate will have a proven track record of steady progress in a similar manufacturing environment and must possess a willingness to learn all equipment and jobs in the assigned manufacturing and sanitation of clean room facilities as required. Production Technicians are also responsible for the quality of products produced by ensuring compliance with local, State and Federal regulations, including current Good Manufacturing Practices (cGMP). | 11/03/2025 |
| 266 | Crown Bioscience Kannapolis, NC Research Associate I, Cancer Pharmacology (in vivo) Bachelor's degree in biology, pharmacology, physiology, animal science, or a related field Exp: 0-1 years |
The Research Associate (RA) at Crown Bioscience North Carolina will support the execution of in vivo research studies, contributing to the advancement of oncology and pharmacology research. The RA will work closely with scientists and senior research staff to carry out experiments, maintain animal models, collect and analyze data, and assist in the development of novel research techniques. This position plays a critical role in ensuring the quality and integrity of preclinical studies. | 11/03/2025 |
| 267 | Curia Albuquerque, NM Validation Specialist II Master’s Degree in Mechanical Engineering, or a related field Exp: 1 year |
Key responsibilities include conducting computer system validations to ensure adherence to GxP regulations, including 21 CFR Parts 210, 211, and 820, as well as compliance with Good Automated Manufacturing Practice (GAMP) standards. Ensures that change controls, records, and procedures align with current Good Manufacturing Practices (cGMP) and regulatory expectations. Coordinates validation activities with cross-functional teams to minimize impact on production schedules while ensuring timely execution. Responsible for authoring validation protocols, final reports, and technical summaries for the qualification and release of equipment, systems, instruments, components, and utilities. Support continuous improvement initiatives and provide mentorship to junior validation staff. | 11/03/2025 |
| 268 | Curia Rensselaer, NY Quality Assurance Specialist II Master’s Degree in Biomedical Engineering, or a related field Exp: 1 year |
Curia Global Inc. (Rensselaer, NY) seeks a Quality Assurance Specialist II for its Rensselaer, NY location. The position is responsible for assisting with validation activities throughout the plant and coordinate appropriate support. Assist in completing validation activities and provide technical assistance to Engineering Services, R&D, Production, Maintenance and QA/QC in Validation and Quality Assurance-related issues. | 11/03/2025 |
| 269 | Curia Hopkinton, MA Quality Control Lab Technician I Bachelor’s degree in Chemistry, Biology or related science Exp: 0-1 years |
The principal responsibility of Quality Control Lab Technician I is the analysis by multiple procedures of intermediates and target compounds. This role is expected to demonstrate expertise in both the theoretical and practical aspects of analytical chemistry. A major component in the scientist's performance rating will be based on productivity. In general, the Quality Control Lab Technician I provides technical, organizational and compliance support for 170+ ongoing stability studies. The incumbent is encouraged to display a degree of professionalism reflected in part by increasing the scientist's knowledge of theory and practice through reading scientific journals and texts at times beyond the "normal" working hours. | 11/03/2025 |
| 270 | Curia Rensselaer, NY validation Specialist II Bachelor’s degree in Chemistry or related field Exp: 0-3 years |
The Quality Control Analyst I is responsible for performing routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished APIs, and stability samples. This role also participates in special projects, method development/transfers and cleaning study qualifications. | 11/03/2025 |
| 271 | Cytiva Pensacola, FL Electrical Project Engineer Bachelor’s degree in engineering (electrical preferred) Exp: 1+ years |
The Electrical Project Engineer is responsible for the Design, Implementation, and Qualification of membrane manufacturing equipment (electrical portions). This includes component and vendor selection as well as contractor supervision. | 11/03/2025 |
| 272 | Dexcom San Diego, CA Systems Engineer 2 - Mobile and Wearable Software Master’s degree Exp: 0-2 years |
Join a passionate team of engineers who are truly making a difference in the lives of people living with diabetes. As the Systems Engineer 2 – Mobile and Wearable Software, you'll be central to ensuring our Dexcom mobile and wearable applications meet the highest standards of safety, usability, and performance. Join our collaborative Systems Engineering team and contribute to technology that empowers users to manage their health with confidence through intuitive, cutting-edge software. If you're driven, thrive in a fast-paced environment, and passionate about turning complex needs into robust software requirements, this is the team for you! | 11/03/2025 |
| 273 | Dexcom San Diego, CA Process Development Engineer 2 Master’s degree Exp: 0-2 years |
The Sensor Process Development team provides global ownership and supports sensor development and manufacturing. As part of the Operations organization, the team ensures process modernization and improvements for sensor safety, sensor accuracy, and sensor reliability resulting in positive outcomes for our users every day. The team has expertise across many subject areas and experience levels, leading to a collaborative environment with innovative solutions. This role will support technical projects related to sensor process development and provide expertise in design and understanding process impact on sensor performance. | 11/03/2025 |
| 274 | Diacarta Pleasanton, CA Clinical Laboratory Assistant BS/BA in life science Exp: 0-1 years |
A CLA performs laboratory duties under the supervision of a licensed CLS. This position is for assisting the CLS and for sample processing, equipment operation and maintenance, and documents. | 11/03/2025 |
| 275 | Diacarta Pleasanton, CA Research Associate BS or MS degree in molecular biology or a related field Exp: 0-2 years |
DiaCarta is seeking a highly motivated, independent, and interactive Research Associate to join the R&D function in the company. The new team member will participate in R&D activities with the goal of developing and launching new qPCR, NGS, and branched DNA tests for IVD cancer diagnostics applications. The successful candidate will have outstanding attention to detail, enjoy working in a fast-paced multidisciplinary team environment, and have exceptional hands-on laboratory skills. DiaCarta is a rapidly growing company, so the candidate must be highly motivated and committed to launching their career in an innovative area of molecular diagnostics. This is a full-time role in Richmond, and you will be reporting to the Senior Scientist. | 11/03/2025 |
| 276 | Diacarta Pleasanton, CA Manufacture Technician BS degree in Molecular Biology, Cell Biology, Biotechnology or related field Exp: 1 year |
Purchase raw materials from a vendor. Receive incoming materials and perform inspection and inventory recording. Production of DiaCarta IVD products to meet sales demands. Labeling of raw materials and finished goods. Perform calibration or preventative maintenance of the instrument. Participate in process improvement projects. Compliance with corporate quality systems. Other on-the-job assignments indicated by management | 11/03/2025 |
| 277 | DM Clinical Research Houston, TX PBMC Lab Technician Bachelor’s degree Exp: 1-2 years |
A PBMC Laboratory Technician will be responsible for conducting special laboratory procedures for clinical trials performing high complexity laboratory techniques including, but not limited to routine isolation of peripheral blood mononuclear cells (PBMC), or other laboratory procedures, etc., ensuring safety measures are followed by facilitating laboratory operations. | 11/03/2025 |
| 278 | Endo Hobart, NY Process Engineer BS degree in Industrial, Manufacturing, Chemical Engineering or Packaging Engineering/Technology or related field Exp: 1-3 years |
Improves safety, quality, and productivity of a fast-paced solid dose pharmaceutical operation. Consistently seeks for and evaluates methods to improve overall customer satisfaction through improved manufacturing efficiencies. Serve as the main point of contact for manufacturing and/or packaging processes in their area regarding safety, quality, and continuous improvement activities. | 11/03/2025 |
| 279 | Enovis Austin, TX Quality Engineer Bachelor’s degree in Engineering, Life Sciences, or a related field Exp: 0-2 years |
We are seeking a detail-oriented and proactive Quality Specialist to join our Quality Department in Austin, TX. This fast-paced role is ideal for someone passionate about quality systems, metrics, and continuous improvement. You will play a key role in supporting and managing quality processes including Field Actions, CAPAs, SCARs, and NCMRs, ensuring full compliance with internal procedures and regulatory standards. Reporting directly to the QMS Manager, this position is responsible for maintaining and reporting critical quality metrics that reflect the overall health of plant operations and production/quality controls. These metrics are regularly shared with senior leadership and cross-functional teams to drive performance, accountability, and compliance across the organization. | 11/03/2025 |
| 280 | EnPlusOne Watertown, MA Research Associate - Synthesis Bachelor’s degree in Molecular Biology, Biochemistry or Chemistry Exp: 1 year |
Your primary role as a Research Associate on the Synthesis team at EnPlusOne is to support the enzymatic RNA synthesis platform. You will assist staff scientists in RNA synthesis, reaction screening, data analysis, buffer preparation, QAQC, and inventory. You will work on multiple internal projects and external collaborations. You will be expected to keep a well-documented lab notebook, stay highly organized, use good communication, and collaborate well with our awesome team. Successful candidates are self-starters who are endlessly curious, excited by research, and flexible in a fast-paced, constantly evolving field. | 11/03/2025 |
| 281 | Enveda Boulder, CO NMR Scientist M.S. Exp: 1-3 years |
At Enveda, every role drives impact. As a NMR Scientist, you’ll be at the forefront of delivering hope to patients everywhere. Your expertise in NMR spectroscopy, instrument maintenance and structure elucidation will be critical in accelerating our mission to advance our pipeline of novel small-molecule therapeutics because every breakthrough starts with bold questions and brave actions. | 11/03/2025 |
| 282 | BioMarin Novato, CA Research Associate, Process Analytics Bachelors degree in biological sciences Exp: 1-2 years |
The Analytical Sciences department at BioMarin Pharmaceutical Inc. is seeking a skilled Analytical Biochemist and/or Biologist at the Research Associate level to join a team focused on supporting gene therapy & enzyme replacement therapy. The successful candidate will be a self-motivated, independent and critical thinker who has experience of working in a multi-disciplinary and fast-paced environment, and solid communication skills. The candidate will execute a wide variety of analytical methods and assays for the characterization of therapeutic candidates in development with a particular focus on testing to support clinical and commercial process development teams. | 10/27/2025 |
| 283 | Biomerics Salt Lake City, UT Staff Design Transfer Engineer Master Degree in Engineering Exp: 1+ years |
The Staff Design Transfer Engineer will be responsible for designing and developing complex medical devices from concept to production, ensuring they exceed customer expectations. You will be expected to work directly with customers to understand product needs, define process specifications, develop manufacturing processes, and build and test devices to those specifications. This role will focus mainly on the processes and fixtures required to consistently manufacture endoscopes. This role collaborates early in the concept phase to guide the team toward manufacturability and repeatability of a design. This role is expected to bring relevant experience to the team and improve the design or process to exceed our customer expectations. | 10/27/2025 |
| 284 | Biomerics Salt Lake City, UT Design Transfer Engineer Master Degree in Engineering Exp: 1+ years |
The Design Transfer Engineer will be responsible for designing and developing complex medical devices from concept to production, ensuring they exceed customer expectations. You will be expected to work directly with customers to understand product needs, define process specifications, develop manufacturing processes, and build and test devices to those specifications. This role will focus mainly on the processes and fixtures required to consistently manufacture endoscopes. This role collaborates early in the concept phase to guide the team toward manufacturability and repeatability of a design. This role is expected to bring relevant experience to the team and improve the design or process to exceed our customer expectations. | 10/27/2025 |
| 285 | bioMérieux Lombard, IL QC Analyst Bachelors degree in biology or related field Exp: 0-3 years |
We are seeking a detail-oriented and motivated Quality Control (QC) Analyst. This role will support the quality of our products. This position must prioritize lots to ensure schedule and goals are met. Responsible for ensuring performance testing meets data specifications. Perform all duties using safety conscious practices. This is an excellent opportunity for individuals passionate about quality and continuous improvement within a manufacturing industry. | 10/27/2025 |
| 286 | bioMérieux Salt Lake City, UT BioReagents Formulator Bachelor’s degree with an emphasis on a biological science Exp: 1+ years |
The Bioreagents Formulator position plays a vital role in the manufacturing and quality process by preparing high-precision reagents and buffers that power our diagnostic testing platforms. This individual will be responsible for the formulation of PCR master mixes, process controls, and large-scale buffers that are later integrated into test kits by our production teams. Accuracy, consistency, and adherence to quality standards are essential as the materials produced directly support our customers’ ability to deliver reliable results to patients worldwide. | 10/27/2025 |
| 287 | Bio-Rad Irvine, CA Production Chemist I Bachelor’s degree in a life science or related field Exp: 0-3 years |
Formulates products and intermediates utilizing biologicals and chemicals of varying properties and characteristics in order to meet specifications | 10/27/2025 |
| 288 | Bio-Rad Fort Worth, TX Manufacturing Engineering Tech I Bachelor’s degree in Engineering, Biotechnology, or a related scientific/technical discipline Exp: 1-5 years |
The Manufacturing Engineering Technician’s day begins with reviewing maintenance and calibration schedules, coordinating with vendors, and ensuring production equipment is operational and compliant. Throughout the day, they troubleshoot issues, perform IOPQ testing, support R&D and manufacturing engineers with experiments or prototypes, and coordinate facility-related tasks. They also update procedures, assist with QN/NC/CAPA documentation, research equipment or components, and provide hands-on support for manufacturing activities as needed. | 10/27/2025 |
| 289 | BioRestorative Therapies Melville, NY cGMP Bio -Manufacturing Engineer MSc degree in cell biology or similar discipline Exp: 1-6 years |
BioRestorative Therapies, Melville, NY is recruiting for a cGMP bio-manufacturing engineer. This role provides outstanding opportunities for talented self-motivated individuals, ideally with experience in (stem) cell biology, immunology, and/or molecular biology, who can contribute to our ongoing efforts to generate clinical grade cell-based therapeutics. We are most interested in connecting with qualified individuals who aspire to support the development of therapeutics and/or life science products and tools to support research endeavors. | 10/27/2025 |
| 290 | Bio-Techne Minneapolis, MN Advanced Research Associate Master’s degree in biological sciences Exp: 0-2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins and monoclonal antibodies for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for production, media and supplement preparation, and additional duties as assigned. | 10/27/2025 |
| 291 | Bio-Techne Minneapolis, MN Research Associate - QC Stem Cell B.S. degree in Biochemistry, Chemistry, Biology, or a related field Exp: 0-2 years |
Performing routine quality control testing of stem cell products using protocol-defined assays to demonstrate their activity. The assays include culturing and handling of stem cells, primary cells, and basic cell lines for use in flow cytometry and immunocytochemistry (ICC). The position requires routine documentation, data analysis and good communication of results. Good Manufacturing Practice (GMP) documentation and workflow is required. Other duties include instrumentation maintenance, reagent preparation and routine lab support for QC antibody testing using western blot, simple wes and immunohistochemistry. | 10/27/2025 |
| 292 | Bio-Techne Minneapolis, MN Research Associate - Conjugation Bachelor’s degree in chemistry, biological sciences, or equivalent Exp: 0-2 years |
As a Research Associate in the Conjugation lab, you will be responsible for preparing conjugated proteins, antibodies, enzymes, oligonucleotides, and microparticles for both manufacturing and research purposes. In addition, you may help prepare and test other chemistry related reagents for manufacturing and QC teams. | 10/27/2025 |
| 293 | Bio-Techne Minneapolis, MN Research Associate - QC Bioassay Bachelor’s degree in the biological sciences or equivalent Exp: 0-2 years |
The Bioassay Quality Control department provides team members the opportunity to practice and learn a variety of laboratory techniques. This position is responsible for performing protocol-defined bioassays on proteins and antibodies to demonstrate the activity of a product. The position requires maintenance of cell lines and isolation of primary cells for use in the assays. Good Manufacturing Practice (GMP) documentation and workflow is required in this position. | 10/27/2025 |
| 294 | Bio-Techne Minneapolis, MN Research Associate - Cell Culture Bachelor’s degree in a biological science Exp: 0-2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins and monoclonal antibodies for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for production, media and supplement preparation, and additional duties as assigned. This position requires weekend work with a Tuesday to Saturday shift. | 10/27/2025 |
| 295 | BioSpectra Bangor, PA Qualification Specialist Bachelor’s degree in Science, Engineering or other related discipline Exp: 1 year |
This position is responsible for ensuring that equipment, systems, and processes are qualified and validated in accordance with regulatory requirements and BioSpectra’s standards. This includes developing, executing, and reporting on equipment, instrumentation, and control system qualifications and re-qualifications | 10/27/2025 |
| 296 | Blueprint Medicines Cambridge, MA Associate Scientist Biology Master’s degree in Bioengineering, Biomedical Engineering, or a closely related biological or life sciences field Exp: 1 year |
Research, identify, and validate novel oncology targets and small molecule drug discovery, utilizing knowledge of bioengineering to develop and conduct cellular assays to support Blueprint Medicine’s novel drug discovery efforts. | 10/27/2025 |
| 297 | Boston Scientific Maple Grove, MN Quality Engineer II Master’s degree in engineering Exp: 1+ years |
Quality Engineer II will be a key member of the Nitinol Shape Memory team supporting the self-expanding component product lines. This role will partner with representatives from the Manufacturing Engineering and Production functions. The person in this role will take the lead in addressing quality issues in a dynamic production environment. The ideal candidate will be comfortable interfacing with downstream internal customers and providing quality leadership to a production team running across 4 shifts. | 10/27/2025 |
| 298 | Bristol Myers Squibb Bothell, WA Specialist - MSAT Cell Therapy Engineering Services, Process Support BS and/or MS degree in Science or Chem/Bio Engineering Exp: 1+ years |
The primary focus of the Specialist - MSAT Cell Therapy Engineering Services, Process Support is to provide product and process support to Cell Therapy Manufacturing Operations at Bristol Myers Squibb’s GMP facility in Bothell, WA. | 10/27/2025 |
| 299 | Bristol Myers Squibb Bothell, WA Associate I, Manufacturing Bachelor's degree in related field Exp: 0-1 years |
Our Associates perform a crucial role in driving our novel cell therapy programs by supporting routine manufacturing operations. We are searching for innovative, intellectually curious individuals with a general understanding of Good Manufacturing Practices (GMPs) to support routine manufacturing operations for Cell Therapy. Successful candidates must be goal-oriented and flexible, with the ability to work effectively and efficiently on a team while demonstrating safety, quality, and GMP compliance at all times. | 10/27/2025 |
| 300 | Bristol Myers Squibb Bothell, WA Associate II, Manufacturing Labels & Issuance Bachelor's degree in related field Exp: 1+ years |
This role is part of the Bothell Manufacturing Logistics & Services team and will focus supporting cGMP Manufacturing Operations for the BMS Bothell site, including the coordination, issuance, reconciliation, and management of production labels and records. Functional responsibilities include all batch label and documentation control activities for Cell Therapy Operations (CTO), including performing and maintaining a GMP compliant clinical and commercial batch documentation and label issuance and control process. | 10/27/2025 |
| 301 | Bristol Myers Squibb New Brunswick, NJ Kilo-Lab Associate Scientist MS in Chemistry or Chemical Engineering Exp: 0-2 years |
The Associate Scientist is required to possess mechanical aptitude and the ability to perform tasks involving manual work. While supporting personnel are available to assist with material handling and equipment setup, the Kilo Lab Associate Scientist is responsible for overseeing and conducting batch activities. Typically, the Kilo Lab handles processes ranging from laboratory-scale up to 200L vessels. This facility serves as a testing ground for new manufacturing technologies, such as flow chemistry and emerging methodologies, in which the scientists frequently participate. | 10/27/2025 |
| 302 | Bristol Myers Squibb Devens, MA Sr. Specialist, QC Analytical Bachelor’s degree in science, engineering, biochemistry or related discipline Exp: 1-3 years |
The Senior Specialist, QC Analytical, Cell Therapy is responsible for supporting Quality Control bioanalytical testing for method validation, critical reagent qualification, in-process, release, and stability testing of clinical and commercial cell therapy drug product. This includes the ability to interface with multiple groups, the ability to independently perform tasks, interpret results, and troubleshoot. Additionally, the QC Senior Specialist will assist with training and assay transfer. The QC Senior Specialist role is stationed in Devens, MA and reports to the Manager, QC Analytical for the Devens CTF. | 10/27/2025 |
| 303 | Bristol Myers Squibb Devens, MA Specialist, Associate Process Engineer, Cell Therapy BSc and/or MSc degree in Science or Chem/Bio Engineering Exp: 0-3 years |
The Specialist, Associate Process Engineer, Cell Therapy provides technical support to the Devens Cell Therapy Facility (CTF) Manufacturing processes in a GMP environment. Technical support includes troubleshooting process and equipment related issues that occur during the Manufacturing process. The Associate Process Engineer works closely with the Manufacturing and Quality teams to determine immediate corrective actions for deviations, identifies root cause, and implements long-term preventive actions. Other responsibilities include participation in process tech transfer, supports incoming process changes by communicating the changes to applicable departments, and participates in process improvement projects at the site. The process engineer works to identify and drive continuous improvements to the manufacturing process. | 10/27/2025 |
| 304 | Bristol Myers Squibb Devens, MA Associate, QC Microbiology, Cell Therapy Bachelor's degree preferred in science Exp: 0-2+ years |
Bristol Myers Squibb is seeking a Associate, QC Microbiology, Cell Therapy to join our QC Microbiology team at the Cell Therapy Facility (CTF) in Devens, MA. Responsible for supporting QC testing for in-process, final product, stability samples and for supporting environmental and facility monitoring. May assist with documentation, deviations, investigations, and continuous improvement efforts. | 10/27/2025 |
| 305 | Bruker Kirkland, WA Staff Electromechanical Technician BS degree in electronic engineering Exp: 0-3 years |
The Bruker AXS-EM division is looking for an electromechanical technician to do board level debugging of PCBs on our electron microscope products. Bruker AXS-EM electronics span a wide range from high-speed digital cameras and scanning systems to ultra stable precision current supplies to 200kV high voltage supplies with tens of millivolt stability. The successful candidate will be able to handle multiple projects simultaneously, making sure that things come together in a timely manner. Help others as needed. Responsibilities will shift and grow based on ability and interests. Light travel to Asia and Europe is a possibility but not a requirement. | 10/27/2025 |
| 306 | Cambrex High Point, NC Scientist 1 - QC M.S. in Chemistry or related field Exp: 0 years |
The Scientist 1 - Quality Control role perform routine analytical testing on raw materials, intermediate, and final products as well as in-process testing; perform data entry; draft deviations, and participate in OOS investigations for their testing with some supervision. Ensure compliance with applicable Company SOPs and regulatory guidance’s. | 10/27/2025 |
| 307 | Cambrex Waltham, MA Associate Chemical Engineer Bachelor’s or Master’s degree in Chemistry, Chemical Engineering, or a related discipline Exp: 1-3 years |
Snapdragon Chemistry is currently seeking exceptional candidates to join the Engineering and Manufacturing team in Waltham, MA. A successful candidate will be joining a group of innovative and entrepreneurial engineers and scientists, with broad deliverables including the development of reactor systems and purifications for continuous flow processes, delivery of high quality, complex chemical matter to our clients, and transferring process technology to clients at their facility. The ideal candidate will have a degree in chemical engineering with experience and a passion for developing new process technology. The candidate should enjoy building equipment and carrying out process development and manufacturing activities in a laboratory or kilo-laboratory environment. The candidate should be well versed in process development and scale-up activities, including common reaction, separation and purification techniques, such as working with 10-100L batch reactors, liquid-liquid extractions, vacuum distillation, filtration, and crystallization. Experience with the development of reactions in flow is preferred but not required. Candidates must possess strong written and oral communication skills. | 10/27/2025 |
| 308 | Candel Needham, MA Contract Research Associate – Virology MS in Virology, Biotechnology, or related field Exp: 1-3 years |
We are seeking a highly motivated and collaborative Research Associate with a strong foundation in virology to support the development of next-generation HSV-1 viral immunotherapy candidates. This individual will contribute to the enLIGHTEN™ Discovery Platform through hands-on experimental work, including viral vector testing, mammalian cell culture, and virology-specific assays. The ideal candidate will bring a passion for innovation and a desire to work in a fast-paced, cross-functional research environment. | 10/27/2025 |
| 309 | Capricor Therapeutics San Diego, CA Manufacturing Associate Bachelor’s degree in Biomedical Engineering, Biological Sciences, or a related field Exp: 1-3 years |
As a Manufacturing Associate I/II, you’ll be a vital part of Capricor’s efforts in delivering therapies for patients in need. Supporting critical clinical trials and exosome development, you’ll perform meticulous production tasks and documentation to uphold our quality and compliance standards. This role places you in a cleanroom environment, where precision and attention to GMP standards are essential. You’ll be instrumental in ensuring that each production step is performed with accuracy, ultimately contributing to Capricor’s therapeutic success. | 10/27/2025 |
| 310 | Capricor Therapeutics San Diego, CA MSAT Training Specialist Bachelor’s degree in life sciences or equivalent Exp: 1-3 years |
As an MSAT Training Specialist at Capricor, you will play a pivotal role in ensuring operational excellence and GMP compliance across our cell therapy manufacturing processes. This position focuses on designing and delivering robust training programs, mentoring manufacturing personnel, and maintaining documentation that supports regulatory readiness and high-quality production. Ideal candidates thrive in a dynamic biotech environment, combining technical expertise with a commitment to continuous improvement and team development. | 10/27/2025 |
| 311 | Caris Phoenix, AZ Molecular Technologist, Solid Tumor Bachelor’s or Master's degree in scientific field Exp: 0-1 years |
The Molecular Technologist – Solid Tumor is responsible for performing various high complexity molecular techniques that include but are not limited to nucleic acid extractions and next generation sequencing (NGS). This position works under the direction of the supervisor and follows standard laboratory procedures and policies. | 10/27/2025 |
| 312 | Carlsmed Carlsbad, CA Clinical Engineer BS or MS degree in a technical field such as Engineering, Life Sciences, Computer Sciences, Mathematics or related medical/scientific field Exp: Entry Level |
The Clinical Engineer is a skilled data-savvy contributor who receives and organizes inbound clinical data in various formats from multiple research sites engaged in Carlsmed-sponsored studies. The role involves receiving, vetting, and forwarding medical images to measurement services and parsing large data sets into subsets for analysis. | 10/27/2025 |
| 313 | Castle Biosciences Pittsburgh, PA Lab, Molecular Technologist Bachelor of Science Degree in Chemistry, Biology, Clinical Laboratory Science, or Medical Technology Exp: 1-2 years |
A typical day for the molecular technologist includes RNA extraction utilizing a mixture of manual and automated methods, RT-PCR performed via manual pipetting, and sample loading on array chips for final result determination. The technologist would be working with equipment setups for all processes, as well as reagent preparations, specimen management, and assisting with inventory and quality management tasks as needed. This role will spend the most time on specimen management and preparation, in-house control creation and reagent Q.C. testing, and quality control checks and documentation associated with high complexity clinical laboratory testing. | 10/27/2025 |
| 314 | Catalent Kansas City, MO BioAnalytics Laboratory Technician Bachelor’s degree in scientific field Exp: No exp |
Catalent Pharma Solutions in Kansas City, MO is hiring a BioAnalytics Laboratory Technician. The BioAnalytics Laboratory Technician supports the BioAnalytics team by performing basic analytical and Good Manufacturing Practices (GMP) testing, maintaining laboratory operations and equipment, and ensuring compliance with safety and quality standards. This role is ideal for individuals beginning their careers in life sciences or pharmaceutical industry. Training will be provided, and the technician will work under close supervision while developing technical skills and regulatory knowledge. | 10/27/2025 |
| 315 | Catalent Kansas City, MO Controlled Substance Specialist II Bachelor's degree Exp: 1+ years |
Catalent Pharma Solutions in Kansas City, MO is hiring Controlled Substance Specialist II. The Controlled Substance Specialist II will support the state of DEA regulatory compliance of controlled substances at the KCM site through the following: oversee the inventory and other aspects regarding the use and storage of controlled substances in pharmaceutical dosage forms in development, laboratory, manufacturing, and packaging environments. Support all necessary regulations with DEA 21 CFR 1300 to end, Bureau of Narcotics and Dangerous Drugs and state licensure, state reporting and maintaining NABP Drug Distributor Accreditation. | 10/27/2025 |
| 316 | Catalent Madison, WI Associate II - Quality Assurance Bachelor's Degree in STEM discipline Exp: 1 year |
The Quality Assurance Operations group has oversight of the manufacturing areas, including process technology transfer, master batch record review and approval, on-the-floor support, product disposition, and shipping. | 10/27/2025 |
| 317 | Catalent Greendale, IN Engineer, Manufacturing, Sciences, and Technology M.S. in Chemical Engineering, Chemistry, Biology, Life Sciences or a related field Exp: 1+ years |
The Engineer, Manufacturing Sciences and Technology (MS&T) is responsible for supporting GMP manufacturing operations as a project leader to commercialize new products and optimize commercial manufacturing processes. The Engineer, MS&T assists in translating client and process development information into cGMP process implementation. | 10/27/2025 |
| 318 | Catalent Winchester, KY Quality Assurance Associate Bachelor's Degree Exp: 1+ years |
The Quality Assurance Associate is responsible for the Quality support functions associated with the manufacturing of solid oral dosage products. The QA Associate is responsible for the oversight of the manufacturing operations (as dictated by cGMP, CFR, and Catalent SOP) through document review/approval, real time monitoring/approval of manufacturing activities and testing/approval of in-process and finished product samples. | 10/27/2025 |
| 319 | Catalent Greenville, NC Project Engineer I Master's degree in Engineering Exp: 1 year |
The Project Engineer I will assure projects are executed in accordance with current site methodologies, policies, industry best practices, and cGMP requirements. The role will leverage the knowledge of GMPs and manufacturing processes to ensure that projects are executed with minimal disruption to operational schedules and must provide construction management oversight to ensure that projects are completed safely, efficiently, and in accordance with all applicable codes and requirements. | 10/27/2025 |
| 320 | Catalent St. Petersburg, FL Associate Scientist II, QC BS or BA in related sciences Exp: No exp |
The Associate Scientist II, Quality Control will independently test, develop and implement assays useful for the identification and characterization of Raw Materials, pre-capsulation, Stability and Finished Products. In addition, this role will Analyze data, document results, maintain laboratory notebook according to cGMP and Internal guidelines, communicate results in written and oral presentations, help in writing Procedures, Specifications and Test Methods. The Associate Scientist II, Quality Control will keep abreast of literature in field; help train colleagues; contribute to continuous improvement within the group, comply with FDA, EPA and OSHA regulations, performing all work in a safe manner and maintain proper records in accordance with all SOP's and policies. | 10/27/2025 |
| 321 | Celerion Lincoln, NE Scientist/ Associate Scientist of Laboratory Automation Bachelor's degree Exp: 1 year |
Celerion is hiring a Scientist/ Associate Scientist of Laboratory Automation to join our Lincoln, NE Bioanalytical team. This role will work onsite daily with our Hamilton, Tecan and Sciclone instruments. In this role, you will perform research and/or development in collaboration with scientific teams and automated systems based on new and existing methodologies. This hands-on role focuses on programming and operating laboratory automation systems with the objective of becoming the subject matter expert for all laboratory automation technologies within our organization. | 10/27/2025 |
| 322 | BioPharmGuy Anywhere, US Contract Data Work some college Exp: 0 yrs |
We are looking for someone with expertise in classifying diseases/conditions by medical specialty to do drug pipeline confirmation tasks. Contract work on a task basis. Must be able to accept payment by PayPal or Venmo. Also must be able to function in the world without using ChatGPT, because if we thought AI could do the task well, you would not be reading this job posting. Please send a message through the contact form if interested. | 09/07/2025 |
| 323 | Bio-Techne Minneapolis, MN Research Associate, Analytical QC B.S. degree in Biochemistry, Chemistry, Biology, or a related field Exp: 0-2 years |
Perform routine quality control testing of protein, peptide or antibody products using standard operating procedures to determine lot status, product release and product stability. Tests include: concentration determination, SDS-PAGE with densitometry, endotoxin assay, TOC, conductivity and other testing as assigned. The position requires routine documentation, analysis and communication of results within the department and across different groups. Other duties include instrument calibration and maintenance, record keeping, and lab support. Within this job function, the Research Associate must also pursue annual goals that aim to facilitate innovation, efficiency, productivity and team building across the QC Department or the entire company. Perform additional duties as assigned. | 10/21/2025 |
| 324 | Bio-Techne San Marcos, CA Chemistry Associate Bachelor’s degree in Chemistry, Biochemistry, Biological Science, or related field Exp: 0-2 years |
Responsible for processing and formulation of controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for manufacturing quality products on schedule. General knowledge and basic application of concepts, theories, terminology and practices that apply to manufacturing in a laboratory environment. | 10/21/2025 |
| 325 | Bio-Techne Minneapolis, MN Advanced Research Associate Master’s degree in a biological science Exp: 0-2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins and monoclonal antibodies for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for production, media and supplement preparation, and additional duties as assigned. This position requires weekend work with a Tuesday to Saturday shift. | 10/21/2025 |
| 326 | Bio-Techne Devens, MA Manufacturing Technician Bachelor’s degree Exp: 0+ years |
Understand and follow appropriate standard operating procedures and work instructions. Regulatory awareness of chemical handling and hazards. Labeling. Safety procedures. Department specific SOP’s. Proper use and basic equipment maintenance. Follow priorities from supervision. Document results, process, and refer to past batch records. Complete all compliance trainings as assigned. Participate in continuous process improvement efforts. Works independently with minimal supervision on routine tasks. Ability to support and help others in the team. Knowledge of work performed by the department and learning how to perform multiple functions within the department. Flexibility to work on multiple tasks with increased effectiveness. Primary operator of manufacturing equipment, including equipment changeovers. Understand and repair minor mechanical issues with manufacturing equipment. Assist in training of new and temporary hires in the Manufacturing Department. Assist with equipment pack line or manual pack line operations. Identify process improvements and flag areas for improvement. Meet quality and productivity expectations. Manages time well and will put in extended time as needed. Willingness to accept changes in work from day-to-day within reasonable and expected boundaries. Perform other duties as assigned within and outside the department. | 10/21/2025 |
| 327 | Bio-Techne Minneapolis, MN Scientific Support Associate Bachelor’s degree in Biological Sciences, Biochemistry, or equivalent Exp: 0-2 years |
Answers and documents incoming customer inquiries by phone, email, and chat. Meets with customers via video conference – Teams, Zoom, Webex, etc., as needed. Addresses inquiries on instrument and software operation, product selection, techniques, procedures, and performs simple troubleshooting. Initiates complaints and works with the appropriate team(s) to resolve. Documents communications and resolutions in Salesforce (CRM, Customer Relationship Management Database). Provides adequate information to the Scientific Support teams to problem solve or to assist with resolution of issue. Communicates with Scientific Support Team, Customer Service, Field Service and Applications, and Sales teams regarding ongoing cases and issues. Documents information and recurring technical issues to support product quality programs and product development. Assists Scientific Support in department functions/projects including but not limited to the maintenance of technical resources, training materials, and FAQs. Supports Marketing and internal teams by providing Voice of Customer. Initiates replacement orders if required by complaint. Is aware of Field Notifications and required actions. Keeps up to date on current technology and use of product lines by attending seminars, reading current scientific literature, and using products in lab. Keeps up to date with training and reading Standard Operating Procedures (SOPs). Follows company policies and practices as outlined in Handbook and follows guidelines regarding safety as outlined in the AWAIR, Chemical Hygiene, and Exposure Control manuals in accordance with the job. Performs additional duties as assigned. | 10/21/2025 |
| 328 | Bio-Techne Newark, CA Quality Control Associate B.S./B.A. in molecular biology, biochemistry, cell biology or related field Exp: 1+ years |
The Quality Control Associate supports all product release testing activities from raw material to finished good products and product stability. This role involves in process testing of incoming raw materials, analytical testing, bulk functional testing, and kit lot release testing in accordance with ISO 13485 GMP requirements. | 10/21/2025 |
| 329 | Alphatec Spine Carlsbad, CA Design Engineer Bachelor’s degree in mechanical or biomedical engineering Exp: 1-4 years |
Under routine supervision, primarily responsible for the enhancement of existing products on our sustaining team. Involved in creating concepts and modeling and drafting designs utilizing 3D CAD software. Other responsibilities include drafting of design history file documents, development of test plans to assess designs, and assisting in the development processes for Manufacturing, Quality Control, Regulatory and Planning for their particular project. | 10/21/2025 |
| 330 | August Bioservices Nashville, TN Manufacturing Technician II/III Bachelor's degree in biological, chemical sciences, or engineering Exp: 1+ years |
August Bioservices is seeking to hire experienced manufacturing technicians to support our growing formulations and filling teams. Headquartered in Nashville, TN – one of the fastest-growing and most exciting cities in the United States – August Bioservices is a privately-owned, high-growth, and high-impact Contract Development Manufacturing Organization (CDMO). As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our work is instrumental in helping to develop molecules today that can become the life-changing therapies of tomorrow. For those seeking dynamic opportunities, rewarding career paths and a chance to make a difference in global health, come grow with August! | 10/21/2025 |
| 331 | Avance Biosciences Houston, TX Laboratory Associate II Bachelor’s degree in biological sciences Exp: 1 year |
Carry out Molecular Biology, Microbiology, and Protein experiments following established SOPs and/or the guidance of laboratory management. Perform DNA/RNA extraction, quantification, and gel QC. Perform PCR setup for qualitative and quantitative analysis. Report experimental results to project managers in a timely manner. Follow established quality management policies and GLP and GMP practices. | 10/21/2025 |
| 332 | Avantor Paris, KY Quality Technician Bachelor’s degree in a science discipline Exp: 1+ years |
Conducting routine and non-routine chemistry and microbiological analysis of raw materials, in-process formulations, and final products to established specifications. Working independently with limited direct supervision. Following through on multiple projects and being a goal-oriented achiever. Demonstrating business-level interpersonal and organizational skills. Wearing a half-face respirator if required. Utilizing and operating laboratory equipment and instruments according to laboratory work instructions or procedures such as pH, conductivity, UV, KF, FTIR, and titrations. Performing chemical tests requiring manual dexterity and sensory discrimination as these tests involve measuring, weighing, and other precise tasks. Completing Resource Conservation and Recovery Act (RCRA) training. Understanding and following written and verbal instructions. Understanding and following Quality Control test methods or compendia methods (USP, EP, BP, JP, or ACS) and EXCIPACT standards. Supporting department management and performing defined tasks to comply with and maintain the site’s ISO 9000/1400 certification and all regulatory requirements. Initiating operation shutdowns and notifying management if questions regarding compliance or issues requiring additional attention arise. Regulatory requirements include, but are not limited to, cGMPs, EPA, OSHA, DEA, DOT, and other applicable local, governmental, and company guidelines. Calculating and generating data for compliance to specifications and reporting results. Performing technical review of lab data forms such as water, environmental monitoring, and direct measure analysis. Calibrating and maintaining lab equipment. Entering results and raw data for tested materials or products in LIMS (Laboratory Information Management System) as needed. Conducting investigative analysis to support investigations, complaints, or instrument troubleshooting. Performing environmental monitoring duties, which require gowning into cleanrooms and collecting air and surface samples while in cleanroom environments. Reviewing for discrepancies in data, manufacturing COAs, COCs, and performing data verification in accordance with company procedures. Applying appropriate disposition labels to materials (accepted, rejected, etc.). Handling hazardous materials using all appropriate or mandatory safety PPE and safety equipment. Completing documentation in a legible manner and reviewing for accuracy. Performing other duties as assigned. | 10/21/2025 |
| 333 | Avantor Waltham, MA Sr. Lab Technician-Media/Buffer Bachelor’s degree in a scientific discipline Exp: 1-2 years |
In this role, you will report to the Onsite Supervisor and will work closely with the Avantor’s Advanced Laboratory Services professionals to serve our customers by performing customized, mission-based lab work and research protocols that help return time back to science. | 10/21/2025 |
| 334 | Avantor Waltham, MA Sr. Lab Technician-Solvent Management Bachelor’s degree in a scientific discipline Exp: 1-2 years |
In this role, you will report to the Onsite Supervisor and will work closely with the Avantor’s Advanced Laboratory Services professionals to serve our customers by performing customized, mission-based lab work and research protocols that help return time back to science. | 10/21/2025 |
| 335 | Avid Bioservices Tustin, CA Research Associate, Process Development Downstream B.S. degree in a Biological Science Exp: 1-2 years |
The Research Associate, Process Development Downstream will provide laboratory support for Process Development by assisting in the downstream process and/or method development. The Research Associate may be assigned various tasks within the department and outside the department as needed. | 10/21/2025 |
| 336 | Avid Bioservices Tustin, CA Research Associate, Process Development Upstream B.S. degree in a Biological Science Exp: 1-2 years |
The Research Associate in Process Development - Upstream will develop and optimize scalable cell culture processes and contribute to transferring the process to Avid Manufacturing. In addition, the Research Associate will maintain production equipment and will research and implement new methods and technologies to enhance process operations. | 10/21/2025 |
| 337 | Avive Brisbane, CA Quality Engineer, Failure Analysis BS in Engineering (preferably Electrical or Biomedical) Exp: 1-4 ears |
The Quality Engineer, Failure Analysis will be responsible for investigating complaints, internal non-conformances, and collaborating with various teams to ensure thorough investigations of product hardware and software issues. This role will be responsible for generating failure investigations reports, metrics and data analysis. | 10/21/2025 |
| 338 | Boston Analytical Salem, NH Chemist II Bachelor’s degree in Chemistry or a related discipline Exp: 1+ years |
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. | 10/21/2025 |
| 339 | Boston Analytical Salem, NH Microbiologist I, QC BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The QC Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 10/21/2025 |
| 340 | Boston Analytical Salem, NH Microbiologist I, VD BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The Microbiologist conducts validation and feasibility testing for quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 10/21/2025 |
| 341 | Boston Analytical Salem, NH Microbiologist I, MB BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The Microbiologist I conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 10/21/2025 |
| 342 | Boston Analytical Morrisville, NC Microbiologist I, Environmental Monitoring BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The EM Microbiologist I conducts quantitative and qualitative analysis of pharmaceutical industries Environment according to FDA, ISO, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include Sampling of pharmaceutical industries through ISO standards and client specific test protocols. | 10/21/2025 |
| 343 | Boston Analytical Morrisville, NC Sample Control Technician Bachelor’s degree in a scientific discipline Exp: 0-2 years |
The Sample Control Technician is responsible for ensuring that all samples are entered into the Laboratory Information Management System (LIMS) and made available to the lab staff in a timely manner. In addition, this position will manage lab inventory, including but not limited to tracking, shipping, and receiving of materials. As needed, this individual will coordinate and assist the metrology department in calibrations and equipment. This position reports to the Associate Director, Microbiology. | 10/21/2025 |
| 344 | Bachem Vista, CA Chemist Bachelor’s degree in chemistry or related scientific field Exp: 0-2 years |
The Chemist function is to work in a cGMP regulated environment manufacturing active pharmaceutical products (APIs) as well as performing related activities at Bachem. | 10/21/2025 |
| 345 | Baxter Marion, NC Quality Lab Associate I - Bioburden B.S. degree in Microbiology, Biology, or related science Exp: 1 year |
Conduct microbiological analysis on raw materials, solution, and components following approved Standard Operating Procedures in an accurate and timely manner. | 10/21/2025 |
| 346 | Baxter Round Lake, IL Quality Lab Associate I Bachelors degree in Chemistry or Science related degree Exp: 6+ months |
The Position encompasses the biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs. | 10/21/2025 |
| 347 | Baxter Marion, NC Quality Lab Associate III - Validation Analytics Master’s in Natural Sciences Exp: 1-3 years |
Responsible for performance and efficiency of Analytical Validation and Qualification activities. Lead and/or coordinate activities in support of analytical validation operations to ensure safe operations, effective planning, and regulatory compliance in the performance of method, process, cleaning, and stability validations for various chemical products while maintaining high standards for quality and responsiveness to production requirements. | 10/21/2025 |
| 348 | Baxter Round Lake, IL Sr Electrical Engineer Masters in Electrical or Electronics or related Engineering Exp: As the Sr. Electrical Engineer, you will develop creative solutions to challenging problems associated with the design of our new and existing infusio |
This person will be involved with coordinating and managing the Quality Assurance activities in all areas of the production/manufacturing processes. This will consist of ensuring quality standards are met in the manufacturing of products. This person must be able to effectively communicate vital information to various personnel throughout the organization. | 10/21/2025 |
| 349 | Baxter Irvine, CA Sr QA Inspector, QM Lab Bachelors Degree in science-related field Exp: 0-2 years |
Responsible for endorsing process and product quality, efficacy, and safety through the routine assessment of plant operations and finished products. Responsible for ensuring adherence to the regulatory and procedural requirements that govern those operations and products. | 10/21/2025 |
| 350 | Baxter Marion, NC Quality Lab Associate I - Environmental Monitoring B.S. degree in Microbiology, Biology, or related science Exp: 1 year |
Supports the environmental monitoring program by performing testing such as surface testing, viable air monitoring, and air total particle counts. Responsible for conducting routine risk assessments and HEPA filter inspections in clean-rooms. | 10/21/2025 |
| 351 | Boston Scientific Maple Grove, MN R&D Engineer III Master's degree in Mechanical Engineering, Biomedical Engineering, or related field Exp: 1+ years |
We are looking for a dynamic R&D Engineer III to support the growing TheraSphere Y90 franchise. In this role, you will make important contributions to support new product development and exploratory initiatives on the TheraSphere Y90 R&D team. This role offers a unique opportunity to work on a global team developing innovative technologies in the field of interventional oncology! | 10/21/2025 |
| 352 | Boston Scientific Maple Grove, MN Manufacturing Technician II Bachelor’s Degree in Engineering, Technology, or related field Exp: 1 year |
As a Manufacturing Technician II, you are responsible for performing functions associated with all manufacturing operations in daily support of products, processes, materials, and equipment in order to achieve production goals (i.e., quality, delivery, cost, productivity, and safety. Daily tasks include responding to equipment downtimes issues on the production floor, performing routine preventative maintenance on production equipment, and supporting Manufacturing Engineers (ME) in value improvement projects. Most of your time is spent on the production floor, working on equipment, and engaging with our Medical Device Specialists (i.e. MDS operators). With General Supervision, you will work on 1st shift as part of a technician team in the Nitinol Shape Memory (NSM) business unit. NSM 1st shift runs Monday-Friday from 5:30am to 1:30pm. | 10/21/2025 |
| 353 | Boston Scientific Maple Grove, MN Electrical Engineer I Bachelor’s degree in electrical or similar Engineering Exp: 0-2 years |
We have an exciting opportunity for an Electrical Engineer I, focusing on New Product Development (NPD), Sustaining, and Compliance on the Coronary Therapies team within the Interventional Cardiology (IC) division here at Boston Scientific. This role will utilize a variety of new and proven technologies to deliver life-changing medical devices to patients and clinicians in support of BSC’s mission. | 10/21/2025 |
| 354 | Boston Scientific Maple Grove, MN Quality Engineer II Master’s degree in engineering Exp: 1+ years |
Quality Engineer II will be a key member of the Nitinol Shape Memory team supporting the self-expanding component product lines. This role will partner with representatives from the Manufacturing Engineering and Production functions. The person in this role will take the lead in addressing quality issues in a dynamic production environment. The ideal candidate will be comfortable interfacing with downstream internal customers and providing quality leadership to a production team running across 4 shifts. | 10/21/2025 |
| 355 | Beckman Coulter Diagnostics Chaska, MN Quality Assurance Engineer I Bachelor’s degree in engineering (i.e. Mechanical or Electrical) Exp: 0-2+ years |
The Quality Assurance Engineer I is responsible for Quality Assurance support for Instrument Manufacturing. This position reports to the Quality Manager and is part of the Instrument Mfg. Quality Assurance team located in Chaska, MN and will be an on-site role. | 10/21/2025 |
| 356 | Beckman Coulter Diagnostics Miami, FL Manufacturing/Process Engineering II Master's degree in Mechanical, Electrical, or Industrial Engineering Exp: 0-2 years |
The Manufacturing/Process Engineering II for Beckman Coulter Diagnostics is responsible to ensure quality meets desired standards, compliance with safety protocols and regulatory standards, provides training to personnel on new processes, equipment and procedures and track and meet key performance indicators. This position reports to the Senior Manager of Technical Operations and is part of the Manufacturing Technical Operations team located in Miami, FL, and is an onsite role. | 10/21/2025 |
| 357 | BD Covington, GA Regulatory Affairs Specialist I BS in a scientific field Exp: 1+ years |
Provide regulatory support through the product life cycle on product project teams (e.g., developing regulatory strategies, timeline development, change control and preparing submission related documents). Prepare and audit 510(k)s, IDEs, PMA and/or international submissions as required. Provide technical collaborate with FDA and international reviewers and respond to questions. Provide timely review and approval of product labeling and marketing claims for regulatory compliance. Provide support required for CE marking activities, including preparation and maintenance of product technical files and clinical evaluations | 10/21/2025 |
| 358 | BD Salt Lake City, UT Engineer II - Research and Development Bachelor's degree (preferred) in STEM or related field Exp: 0-5+ years |
BD (Becton Dickinson and Company), a leading global medical technology company, is seeking a Research and Development Engineer II to work on the sustainability and development of medical devices for BD’s healthcare products. They assume the technical role of projects and champion technical and architectural excellence. The candidate should be passionate about solutions to clinician and patient unmet needs, and enjoy the details involved with the long-term outlook of technological solutions to clinical needs. The position is an exciting opportunity to make a meaningful, positive impact on patients throughout world by leveraging cutting edge technologies. | 10/21/2025 |
| 359 | BD San Diego, CA Biochemist II - Bead Manufacturing Master’s degree in a science-related field Exp: 1-3 years |
The Biochemist II, Beads Manufacturing must have working knowledge of fluorescence microparticle manufacturing. This role will conduct data analysis to solve complex problems with various factors. The Biochemist II is responsible for improving process efficiencies and product quality. This position will also support and participate in continuous improvement projects as identified by the leadership team and assigned by the Manager. | 10/21/2025 |
| 360 | BioAgilytix Durham, NC Analyst II (Cell-based GMP) Master's degree in molecular biology, biochemistry, immunology, biotechnology, or related field Exp: 1 year |
We are looking for candidates who have scientific lab experience in a deadline-driven setting. The best candidates are people who have hands-on experience in a lab environment (academic or professional) and are curious about applying different scientific methods, equipment and extraction processes. If you are a person who is energized by project variety and learning from top scientists in our industry, then you’ll be right at home here at BioAgilytix. | 10/21/2025 |
| 361 | bioMérieux Salt Lake City, UT BioReagents Formulator Bachelor’s degree with an emphasis on a biological science Exp: 1+ years |
The Bioreagents Formulator position plays a vital role in the manufacturing and quality process by preparing high-precision reagents and buffers that power our diagnostic testing platforms. This individual will be responsible for the formulation of PCR master mixes, process controls, and large-scale buffers that are later integrated into test kits by our production teams. Accuracy, consistency, and adherence to quality standards are essential as the materials produced directly support our customers’ ability to deliver reliable results to patients worldwide. | 10/21/2025 |
| 362 | BioMarin Novato, CA Manufacturing Associate Bachelor's degree in a science-related area or engineering Exp: 1-2 years |
Operating large-scale bioprocess equipment for Cell Culture, Purification, or Buffer and Media processing; performing all aspects of processing with a broad understanding of science, compliance, and technical aspects; displaying competency with process equipment and automated control systems; performing cleaning and sterilization of parts and equipment used in the manufacturing process; and having knowledge of biotech manufacturing processes and equipment, including cell culture, depth and tangential flow filtration, column chromatography, protein purification and formulation, and/or buffer and media operations. The candidate should have the ability to understand, apply, and evaluate basic chemistry, biology, and scientific principles as appropriate for the position. Proficiency with compliance, adherence to standard operating procedures, batch records, good documentation practices, and data capturing is also essential. | 10/21/2025 |
| 363 | Alcami Wilmington, NC Scientist II - Chemistry Masters degree in Chemistry, Biochemistry, or related field Exp: 0+ years |
The Scientist II (Chemistry) is accountable for driving results in a fast-paced environment by performing analytical routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. For this Scientist II (Chemistry) position, HPLC, TOC, UV, osmolality, density, and pH are commonly employed in the described testing in addition to other key methodologies such as KF and titration. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company) and may also assist with method development / method validation projects. | 10/15/2025 |
| 364 | Alcami Wilmington, NC Scientist II - QC Chemistry Masters degree in Chemistry, Biochemistry, or related field Exp: 0+ years |
The Scientist II - QC Chemistry is accountable for driving results in a fast-paced environment by performing analytical routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. For this Scientist II (Chemistry) position, HPLC, TOC, UV, osmolality, density, and pH are commonly employed in the described testing in addition to other key methodologies such as KF and titration. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company) and may also assist with method development / method validation projects. | 10/15/2025 |
| 365 | Alcon Houston, TX Building Automation Engineer Master’s Degree Exp: 0+ years |
As a Building Automation Engineer, you will be trusted with the design, implementation, and optimization of advanced building automation systems (BAS) across our manufacturing campus. You will work with Johnson Controls (JCI) platforms to integrate HVAC, fire, security, and energy systems, ensuring operational efficiency, regulatory compliance, and environmental control at our Manufacturing Facility in Houston, TX. | 10/15/2025 |
| 366 | Alcon Fort Worth, TX Sr. Optical Engineer - Integrated Optical System Master’s Degree Exp: 0+ years |
The Sr. Optical Engineer is primarily responsible for supporting optical engineering efforts through testing, data analysis, and research to enhance optical system design. You will be expected to collaborate with teams to validate optical models, refine testing procedures, and contribute to the development of high-performance optical solutions. The Sr. Optical Engineer within the Integrated Optical System function will support metrology system development and qualification. | 10/15/2025 |
| 367 | Alcon Fort Worth, TX Sr. Associate, Mechanical Design Engineering Master’s Degree Exp: 0+ years |
We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As a Sr. Associate, Mechanical Design Engineering supporting Alcon's Engineering function, you will be trusted to work on developing innovative intraocular devices and improving quality, processes, products, packaging and materials across our business to help deliver brilliant outcomes. | 10/15/2025 |
| 368 | Alcon Johns Creek, GA Sr. Associate, Facilities Engineer Master’s Degree Exp: 0+ years |
We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As a Sr. Associate, Facilities Engineer supporting the MTO Chemical Team in Johns Creek, GA. | 10/15/2025 |
| 369 | Alcon Johns Creek, GA Sr. Associate, Controls Engineer Master’s Degree Exp: 0+ years |
We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As a Sr. Associate Controls Engineer supporting the U.S. MTO Team in Johns Creek, GA. | 10/15/2025 |
| 370 | Alcon Johns Creek, GA Sr. Associate, Automation and Control Engineering Master’s Degree Exp: 0+ years |
As a Sr. Associate, Automation and Control Engineering, supporting our supporting our Engineering Manufacturing Systems team, you will be trusted to design, implement, install, analyze and/or optimize manufacturing processes, procedures, equipment, and programming. The ideal candidate will also have expertise in PLC and automation controls, ensuring seamless integration and functionality of mechatronic systems to best support our 24/7 operation at Johns Creek, GA. | 10/15/2025 |
| 371 | Alcon Fort Worth, TX Senior Engineer II Master’s Degree Exp: 0+ years |
We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As a Senior Engineer, II supporting mechanical design projects by tackling complex mechanical design tasks, refining components, conducting performance analyses, and troubleshooting. You will be expected to build effective and meaningful relationships with engineering teams and apply advanced modeling and simulation techniques. | 10/15/2025 |
| 372 | Aldevron Madison, WI Scientist I- Downstream PD Master’s in biology, biotechnology, molecular biology, biochemistry, chemistry, or a closely related field Exp: No exp |
The Scientist I position is part of the Downstream Process Development (DSPD) team in the Protein Business Unit of Aldevron. This is an on-site position at the facility located in Madison, WI. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Technical Operations team (encompassing DSPD and other teams) and your responsibilities will revolve around developing processes to purify recombinant proteins from microbial host expression systems. | 10/15/2025 |
| 373 | Alkermes Wilmington, OH Temp-QC Analyst-Microbiology Bachelor's in science, preferably in Biology / Microbiology / Biotechnology or Biochemistry Exp: 1+ years |
QC Analyst I must have broad knowledge of microbiology techniques within the laboratory required for the routine support of the microbiology laboratory operations. In this role the Analyst will be a fully functional member of the team responsible for testing and data entry for finished product, in-process samples, stability samples, clinical materials and raw material release in a cGMP regulated environment | 10/15/2025 |
| 374 | Alkermes Wilmington, OH Process Engineer I/II/Lead-OSD BS degree in Engineering or technical discipline Exp: 0-2 years |
This position will support and assist in manufacturing pharmaceutical products for commercial and clinical supplies. Key duties include scale-up and transfer of oral solid dosage formulations/processes to the production facility, designing and recommending equipment purchases, and writing and executing equipment specification and commissioning protocols. Troubleshoot automated equipment for pharmaceutical formulation and packaging. Identify and implement process/equipment improvements (utilizing Change Control systems) to reduce waste and increase process reliability. Assure the resolution of deviations, corrective actions, action items from Change Control systems, and any audit non-compliance items. Perform process and equipment evaluation (FMEA, etc) to identify risks and weaknesses in new and current processes. Develop and implement SOPs in support of new and upgraded processes. Champion projects as they move into and through the manufacturing areas. Provide regular updates to leadership on project status and issues. | 10/15/2025 |
| 375 | Altasciences Harleysville, PA Senior Formulation Scientist MS in Pharmaceutical Sciences or in a related discipline Exp: 1-3 years |
Senior Formulation Scientist will be responsible for the formulation development for small and complex molecules, including controlled-release, liposomal, and spray-dried dispersions (SDD). This role requires deep expertise in oral and advanced formulation technologies. The scientist will evaluate innovative drug delivery approaches and support development from preclinical through late stage. This position collaborates closely with manufacturing and analytical teams to ensure successful technology transfer for GMP manufacturing. | 10/15/2025 |
| 376 | Altasciences Columbia, MO Necropsy Technician Bachelor of Science (B.S.) Exp: 6 months-1 year |
To provide high quality and timely processing of pathological specimens through gross examinations, necropsies, tissue trimming and tissue processing as specified in company protocols and SOPs. | 10/15/2025 |
| 377 | Altasciences Columbia, MO Scientist, LCMS Bachelor’s degree in Immunology/ Biology/ Chemistry or equivalent discipline Exp: 6 months |
You will assist in daily activities and operation of the Laboratory Sciences department including equipment maintenance, stocking supplies and general cleaning. You will also support and perform data collection activities including primarily focused on mass-spectrometry. | 10/15/2025 |
| 378 | Alturas Analytics Moscow, ID Assistant Scientist Bachelor’s degree in a physical, biological or chemistry science Exp: 1-3 years |
We’re looking for a detail-oriented, team-focused Assistant Scientist to join our dynamic bioanalytical laboratory. We are dedicated to providing ample opportunities for growth and promotion within our team. You’ll work closely with experienced Senior Scientists, gaining hands-on expertise in a supportive and engaging environment. | 10/15/2025 |
| 379 | Amgen New Albany, OH Senior Associate IQA Bachelor’s Exp: 6 months |
In this vital role you will be responsible for sampling, inspection and dispositioning all raw materials received at the facility under general supervision. A key aspect of this role is to apply critical thinking skills to ensure quality and compliance to GMP regulations for all area operations and associated processes. Duties include batch record review, SOP creation & review, documentation, review & approval of minor deviations and CAPA records and batch disposition of raw materials. | 10/15/2025 |
| 380 | Amgen Thousand Oaks, CA Associate Scientist Master’s degree Exp: 1 year |
Let’s do this. Let’s change the world. We are seeking an Associate Scientist with expertise in high-throughput mass spectrometry-based proteomics. In this vital role, you will be part of the Discovery Proteomics team based in Thousand Oaks, CA. The discovery proteomics team delivers key insights into target and drug discovery by supporting pipeline programs and advancing platform technologies through mass spectrometry. In this role, you will drive pipeline advancement and screening platform by performing automated sample preparation and analysis for a range of high-throughput proteomic assays. This position requires hands-on experience with sample preparation for mass spectrometry analysis using liquid handlers, as well as proven expertise in operating high-throughput mass spectrometers. Your contributions will play an important role in high-throughout drug screening and pipeline support. | 10/15/2025 |
| 381 | Amgen West Greenwich, RI Senior Associate Quality Control Bachelor’s Exp: 6 months |
Let’s do this. Let’s change the world. In this vital role you will provide testing support for the QC Night Shift“Team C”(Saturday - Tuesday from 9:45pm – 8:15am)at Amgen Rhode Island. | 10/15/2025 |
| 382 | Amneal Piscataway, NJ Associate Maintenance Engineer Bachelors Degree (BA/BS) Engineering, Pharmaceutics, Industrial Pharmacy, or related field Exp: 1+ years |
The Associate Maintenance Engineer supports the upkeep, optimization, and reliability of pharmaceutical manufacturing equipment and utilities. The successful candidate will assist in the maintenance, troubleshooting, continuous improvement and plays a crucial part in ensuring smooth production of oral solid dosage forms and transdermal systems, including birth control patches. This role is critical to ensuring equipment reliability, operational efficiency, and compliance with GMP and regulatory standards. | 10/15/2025 |
| 383 | Amneal Piscataway, NJ ssociate Automation Engineer Master Degree (MS/MA) Electrical Engineer, Electrical & Electronics Engineer Exp: 1 year |
The Automation Engineer's primary role is to work under supervision and coordinating installation, troubleshooting and assist in maintaining automated processes and facility related equipment. | 10/15/2025 |
| 384 | Applied Medical Rancho Santa Margarita, CA Machine Design Engineer, Automation Bachelor's degree in Mechanical Engineering or in a related field Exp: 1 year |
Are you a visionary Design Engineer? Join Applied Medical and be at the forefront of revolutionizing medical device manufacturing. As part of our Automation team, you will be at our global U.S. headquarters, pioneering cutting-edge machines, collaborating across departments, and leading the way in cost reduction, optimizing manufacturing processes. As a Design Engineer, you will play a vital role in supporting the development of automated machines or automated processes for our in-house medical device manufacturing. It's your chance to make an enduring impact on the future of healthcare. | 10/15/2025 |
| 385 | Applied Medical Rancho Santa Margarita, CA Document Control Engineer I Bachelor's degree in Engineering, Physical or Biological Sciences, another technical discipline, or equivalent Exp: 1 year |
As a Document Control Engineer I, you will be responsible for working within the framework of a team and performing the following activities: Understand and comply with Applied Medical's Quality Systems (QS), safety rules, and company policies. Coordinate and respond to questions and act as a liaison to internal and external customers/ Review, monitor, and approve programs and documentation, as assigned, to ensure compliance with relevant standards, regulations, and guidance documents. Work with Systems, Applications & Products in Data. Processing (SAP) system to understand and maintain material masters, bill of materials (BOMs), and routers. Maintain and improve internal document procedures. Identify and implement systems to improve the overall efficiency of processes within Document Control/ Perform additional duties and responsibilities, as needed | 10/15/2025 |
| 386 | Applied Medical Lake Forest, CA Manufacturing Design Engineer Bachelor’s degree in Mechanical Engineering or related technical field Exp: 1+ years |
Join Applied Medical and be at the forefront of precision medical device manufacturing. As a Manufacturing Design Engineer, you’ll merge engineering creativity with hands-on design expertise, developing equipment and automation solutions to support sub-assembly workflows product integration. In this dynamic, production-facing role, you’ll collaborate with PPD teams, machinists, and cross-functional engineers—applying your CAD skills and mechanical intuition to design tooling, prototype components, and support the build and validation of custom equipment that enhances throughput, quality, and manufacturability across the floor. | 10/15/2025 |
| 387 | Applied Medical Rancho Santa Margarita, CA Complaint Evaluation Engineer Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, Electrical Engineering or a similar engineering discipline Exp: 1 year |
Collaboration is a fundamental part of our organization's culture and is essential to our continued success. As such, the successful candidate for this position is expected to work on-site, enabling them to engage fully with colleagues and contribute to cross-functional initiatives. Therefore, the ability to work collaboratively and contribute to a positive and supportive team environment is a key requirement for this role. | 10/15/2025 |
| 388 | AMT’ Cleveland, OH Quality Manager Bachelor's Degree in Engineering Exp: 1-5 years |
This person will be involved with coordinating and managing the Quality Assurance activities in all areas of the production/manufacturing processes. This will consist of ensuring quality standards are met in the manufacturing of products. This person must be able to effectively communicate vital information to various personnel throughout the organization. | 10/15/2025 |
| 389 | AMT’ Cleveland, OH Quality Assurance Supervisor Bachelor's Degree in Engineering Exp: 1-5 years |
This person will be involved with coordinating and managing the Quality Assurance activities in all areas of the production/manufacturing processes. This will consist of ensuring quality standards are met in the manufacturing of products. This person must be able to effectively communicate vital information to various personnel throughout the organization. | 10/15/2025 |
| 390 | ARL Bio Pharma Oklahoma City, OK Chemist I - Analytical Bachelor’s degree in chemistry or related science Exp: 1-2 years |
Join a company where you can make a difference from day one and help make the world a better and safer place. ARL Bio Pharma provides analytical and microbiological testing for the pharmaceutical industry. Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug manufacturers, and raw material suppliers bringing excellence to pharmaceutical sciences and making pharmaceuticals safer. This position is a fantastic stepping-stone for those with some basic experience looking to expand their career in the interesting world of the pharmaceutical industry. The Chemist I is responsible for utilizing established methods and standard lab equipment/instrumentation (HPLC, IC) to qualitatively and quantitatively analyze routine pharmaceutical substances and formulations. | 10/15/2025 |
| 391 | ARL Bio Pharma Oklahoma City, OK Microbiologist I Bachelor’s degree in Microbiology or related science Exp: 0-2 years |
Under the supervision of the laboratory supervisor the Microbiologist I provides a high level of quality pharmaceutical microbiology testing as well as effective customer service to ARL Bio Pharma clients. This is a safety sensitive position as defined by state and federal laws that will require working with hazardous materials and/or handling medicine. | 10/15/2025 |
| 392 | ARL Bio Pharma Oklahoma City, OK Chemist I - R&D Bachelor’s degree in chemistry or related science Exp: 1-2 years |
Join a company where you can make a difference from day one and help make the world a better and safer place. ARL Bio Pharma provides analytical and microbiological testing for the pharmaceutical industry. Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug manufacturers, and raw material suppliers bringing excellence to pharmaceutical sciences and making pharmaceuticals safer. This position is a fantastic stepping-stone for those with some basic experience looking to expand their career in the interesting world of the pharmaceutical industry. The Chemist I is responsible for utilizing established methods and standard lab equipment/instrumentation (HPLC, IC) to qualitatively and quantitatively analyze routine pharmaceutical substances and formulations. | 10/15/2025 |
| 393 | AstraZeneca Gaithersburg, MD Associate Scientist, Analytical Sciences, GMP Bachelor’s or master’s degree in chemistry, biochemistry or related field Exp: 0-5 years |
Are you ready to dive into the world of Analytical Sciences within GMP regulations? Join our dynamic team responsible for supporting clinical stage biopharmaceutical products. We manage lot release and stability programs, reference standards, critical reagents, and more. Collaborate with experts across multiple analytical disciplines such as chromatography, electrophoresis, immunoassay, bioassay, and device functionality methods. Work closely with Analytical Sciences development personnel, Clinical Supply Chain, CMC, and Quality Assurance throughout all stages of clinical development. | 10/15/2025 |
| 394 | AstraZeneca Frederick, MD Production Technician I -Nights BS/BA degree in STEM field Exp: 0-1 years |
In this role, you will be responsible for the operation of processing equipment according to established SOPs, MPRs, & SPRs in accordance with cGMPs. Your duties will include solution preparation, cell culture, purification & formulation, and supporting activities. You will also train with a qualified Technician on activities related to operating process equipment with the requirement of qualification. Additionally, you will follow and execute cGMP documentation, utilize Manufacturing Execution systems (MES), contribute to problem-solving activities for non-routine activities on the production floor, and participate in continuous improvement activities for Manufacturing. Adherence to AstraZeneca values and behaviors is expected. | 10/15/2025 |
| 395 | AstraZeneca Gaithersburg, MD Scientist, Oncology TCR-T Cell Therapy Master's Degree in Immunology, Cancer Biology, Cell Biology, or relevant scientific field Exp: 1 year |
We are seeking a highly motivated and independent Scientist to join our rapidly growing Cell Therapy Team. In this role, you will contribute to advancing innovative Cell Therapy products by designing and conducting laboratory experiments, developing methodology, and generating and interpreting scientific data in a highly collaborative environment.Expertise inin vitro and in vivo studies and T cell biology is critical for this role. To be successful in this role, you must be well-organized and keep an excellent written record of your work. You will be based in Gaithersburg, MD and report to the Associate Director, TCR-T Cell Therapy. | 10/15/2025 |
| 396 | AstraZeneca Gaithersburg, MD Associate Specialist, Clinical Biologics Bachelor’s degree in a science related field Exp: 0-4 years |
As an Associate Specialist in the clinical production team within Biopharmaceutical Development, you’ll build broad knowledge of bioprocessing in a cGMP environment to launch your career in the biopharmaceutical industry. In this role, you will take an adaptable, science driven approach to everything you do. You will become an integral part of process development, accelerating product candidates into the clinic, and gaining knowledge and experience in cell culture, purification and critical support activities. Under the supervision of highly trained personnel, you will gain the process knowledge and skill sets to perform large scale clinical development activities through hands-on training. You will join a collaborative and driven team in a world class biopharmaceutical company that is driving disruptive innovation in the industry. | 10/15/2025 |
| 397 | Bio-Techne Devens, MA Manufacturing Technician Bachelor’s degree Exp: 0+ years |
Understand and follow appropriate standard operating procedures and work instructions. Regulatory awareness of chemical handling and hazards. Labeling. Safety procedures. Department specific SOP’s. Proper use and basic equipment maintenance. Follow priorities from supervision. Document results, process, and refer to past batch records. Complete all compliance trainings as assigned. Participate in continuous process improvement efforts. Works independently with minimal supervision on routine tasks. Ability to support and help others in the team. Knowledge of work performed by the department and learning how to perform multiple functions within the department. Flexibility to work on multiple tasks with increased effectiveness. Primary operator of manufacturing equipment, including equipment changeovers. Understand and repair minor mechanical issues with manufacturing equipment. Assist in training of new and temporary hires in the Manufacturing Department. Assist with equipment pack line or manual pack line operations. Identify process improvements and flag areas for improvement. Meet quality and productivity expectations. Manages time well and will put in extended time as needed. Willingness to accept changes in work from day-to-day within reasonable and expected boundaries. Perform other duties as assigned within and outside the department. | 10/15/2025 |
| 398 | Bio-Techne Minneapolis, MN Scientific Support Associate Bachelor’s degree in Biological Sciences, Biochemistry or equivalent Exp: 0-2 years |
The responsibilities of this position, Scientific Support Associate (SSA), are to respond to incoming technical inquiries from the Bio-Techne commercial team and Bio-Techne's North American customers, providing first-tier technical and sales assistance for R&D Systems, Tocris, and Novus products. Completes all customer requests including e-mail responses and simple quotes. Maintains technical resources. Backs up Customer Service and Sales departments as necessary. Continues training to stay up to date on technical information for old and new products. Performs additional duties as assigned. | 10/15/2025 |
| 399 | Bio-Techne Minneapolis, MN Research Associate - QC Stem Cell B.S. degree in Biochemistry, Chemistry, Biology, or a related field Exp: 0-2 years |
Performing routine quality control testing of stem cell products using protocol-defined assays to demonstrate their activity. The assays include culturing and handling of stem cells, primary cells, and basic cell lines for use in flow cytometry and immunocytochemistry (ICC). The position requires routine documentation, data analysis and good communication of results. Good Manufacturing Practice (GMP) documentation and workflow is required. Other duties include instrumentation maintenance, reagent preparation and routine lab support for QC antibody testing using western blot, simple wes and immunohistochemistry. | 10/15/2025 |
| 400 | Bio-Techne Minneapolis, MN Research Associate - Conjugation Bachelor’s degree in chemistry, biological sciences, or equivalent Exp: 0-2 years |
As a Research Associate in the Conjugation lab, you will be responsible for preparing conjugated proteins, antibodies, enzymes, oligonucleotides, and microparticles for both manufacturing and research purposes. In addition, you may help prepare and test other chemistry related reagents for manufacturing and QC teams. | 10/15/2025 |
| 401 | Bio-Techne Minneapolis, MN Research Associate - QC Bioassay Bachelor’s degree in the biological sciences or equivalent Exp: 0-2 years |
The Bioassay Quality Control department provides team members the opportunity to practice and learn a variety of laboratory techniques. This position is responsible for performing protocol-defined bioassays on proteins and antibodies to demonstrate the activity of a product. The position requires maintenance of cell lines and isolation of primary cells for use in the assays. Good Manufacturing Practice (GMP) documentation and workflow is required in this position. | 10/15/2025 |
| 402 | Bio-Techne Minneapolis, MN Research Associate - Cell Culture Bachelor’s degree in a biological science Exp: 0-2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins and monoclonal antibodies for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for production, media and supplement preparation, and additional duties as assigned. This position requires weekend work with a Tuesday to Saturday shift. | 10/15/2025 |
| 403 | Vaxcyte San Carlos, CA Associate Scientist II, Drug Product Analytics MSc in Chemistry, Biophysics or Biochemistry Exp: 1 year |
Vaxcyte is looking for an energetic and talented individual to join our Drug Product Development team. The candidate must have knowledge of and practical experience in analyzing and characterizing biomolecules (proteins, polysaccharide conjugates, vaccines) using a variety of methods, including immunoassays, chromatography, spectrophotometric techniques, light scattering, and particle sizing. Experience in analyzing vaccine and adjuvant-containing formulations is a plus. In addition, Vaxcyte is looking for an experienced and flexible individual who would be comfortable working on multiple projects at once, with fluid prioritization to enable aggressive timelines. This position is for a lab-based scientific role and requires excellent scientific judgement, independence, rigor, and thorough record-keeping. | 10/05/2025 |
| 404 | Veracyte South San Francisco, CA Specimen Processor Bachelor’s degree Exp: 0-2 years |
Primarily responsibility for receiving and accessioning specimens, handling specimen documentation, and data entry of requisitions. They are also responsible for keeping the lab in a clean and orderly condition. Specimen Processor I are knowledgeable in sample integrity issues and are a resource to others in the lab. They maintain flexibility regarding work schedules including daily assignments, holiday schedules, and days of the week as determined by business need. | 10/05/2025 |
| 405 | Vertex Boston, MA Process Dev Engineering Scientific Associate Bachelor's degree in Biochemistry, Biological Engineering, Chemical Engineering or a related field Exp: 1 year |
Supports the development of upstream or downstream production processes for cell therapy projects. Supports technology transfer to CMO and provides manufacturing support for GMP production. Supports a fully integrated team to facilitate the success of projects. Utilizes understanding of principles of molecular and cell biology techniques when troubleshooting typical problems. Applies statistical principles to guide process optimization. Conducts cell culture experiments, characterization and data analyses in support of process characterization and improvement. Supports technical reports, regulatory filings, source documents, patents and external publications. Works within departmental teams, supports deliverables and participates in team discussion on issue resolution. | 10/05/2025 |
| 406 | VGXI The Woodlands, TX Quality Control Technician Bachelor’s Degree Exp: 1-3 years |
The Quality Control Technician is responsible for in-process and release testing of products manufactured at VGXI. Will provide support for new assay development, method transfers, risk assessments, assay qualifications, change controls and validations. Set-up, organization, and day-to-day operations of a Quality Control Lab are also required. | 10/05/2025 |
| 407 | Viatris St. Albans, VT Chemist SI, Quality Control Bachelor's degree Exp: 0-2 years |
Performs and documents the analysis of samples following approved test methods. Calculate, check, and/or review data. Assist with method development, validation, and transfer. Assist with instrument calibrations and maintenance. May work on analytical projects under direct supervision. Attend training classes and seminars as required. | 10/05/2025 |
| 408 | Vivex Biologics Miami, FL Quality Control Labeling Inspector Bachelors Exp: 0-1 years |
The QC Labeling Inspector is responsible for maintaining a high level of inventory accuracy and integrity within the Tissue Bank. Performs final product labeling and inspections, manages transport and storage of quarantine tissue, and maintains labeling supplies. Promotes Lean Behaviors across the organization (This includes Participating in Try storming, Brainstorming and Lean Related Initiatives). Promotes Usage of Problem Solving. Ensure that Labeling Operations are in Compliance with the State and Federal Regulations and AATB Standards. | 10/05/2025 |
| 409 | Vivex Biologics Miami, FL Process Engineer I BS or MS in Biomedical, Mechanical or Industrial Engineering or other applicable engineering discipline Exp: 1-3 years |
The Process Engineer I is responsible for evaluating and improving manufacturing processes to reduce cost, improve yields, and reduce variation. This position performs new process design and implementation, process validations and process qualifications. Process Engineers also participate in technology transfer to ensure the processes necessary for new products are effectively translated to manufacturing from R&D. Process Engineer I makes use of statistical analysis methods, critical thinking, process development, and scaling principles to achieve the objectives mentioned above. | 10/05/2025 |
| 410 | Waters Corporation Milford, MA Supplier Quality Engineer I bachelor’s degree in engineering, Mathematics, Business, Science, or related experience in a technical field Exp: 1-2 years |
Waters Corporation is currently seeking a Supplier Quality Engineer I to join our organization. This position is hands-on in a fast-paced environment which will interact with external suppliers and multiple internal functions (R&D, Engineering, Test Engineering, Reliability Engineering, Regulatory, Purchasing, sister manufacturing sites and contract manufacturers) to resolve supplier quality issues. Primary responsibilities will be to analyze and measure supplier performance, implement corrective actions when needed, and draft quality agreements with suppliers to define the requirements between the supplier and Waters. Responsibilities include supplier investigations into product non-conformances, reporting quality system metrics, supporting Statistical Process Control (SPC) initiatives, and driving projects related to product and process quality. The position is also responsible for performing quality audits on suppliers to ensure adherence to Waters expectations. Supplier Quality Engineers act as liaison for quality issues between our production areas, and our RDE, sustaining & test engineering departments and suppliers. | 10/05/2025 |
| 411 | West Kinston, NC Associate Process Engineer, Sterilization Bachelor’s or Master degree in Biology/ Microbiology /Chemistry or another scientific area Exp: 1-3+ years |
This role is key to developing and introducing process improvements, standards, life cycle management and validation in select process areas, helping to advance and transform West’s growing business, supporting capital investments and contributing to addressing complex assignments. This person has decision rights for his process area, and he/she will have the opportunity to drive the implementation of new innovative processes and technologies in cooperation with the engineering and quality assurance teams and the plants. | 10/05/2025 |
| 412 | WuXi AppTec Middletown, DE QC Operation Specialist Bachelor’s degree in Chemistry, Biology, Pharmaceutical Sciences, or related discipline Exp: 1-3 years |
We are seeking a QC Operation Specialist to provide critical operational support to the QC laboratories at WuXi STA’s Middletown, DE site. This role is responsible for stability room and equipment management, sample logistics, and controlled documentation, ensuring QC laboratories operate efficiently, meet testing timelines, and remain in full compliance with GMP and regulatory requirements. The QC Operation Specialist will be a key contributor during both startup and steady-state operations, supporting Analytical and Microbiology QC teams. | 10/05/2025 |
| 413 | WuXi Biologics Cranbury, NJ Process Equipment and Reliability Engineer I Bachelor’s degree in mechanical, Chemical, Bioprocess, or related Engineering discipline Exp: 0-2 years |
The Process Equipment and Reliability Engineer I will provide technical support to ensure safe, reliable, and compliant operation of process and utility equipment within a biopharmaceutical manufacturing facility. An Engineer I, will assist with troubleshooting, preventive maintenance, and reliability initiatives while working within cGMP requirements, engineering systems, and reliability methodologies. This role is designed to build foundational skills in equipment engineering and reliability while contributing to daily operations and long-term asset improvement efforts. | 10/05/2025 |
| 414 | Veranex Providence, RI Manufacturing Engineer 1 or 2 Bachelor’s degree in manufacturing or mechanical engineering Exp: 1-3 years |
Veranex has an exciting opportunity to join our team as a Manufacturing Engineer 1 or 2. You will be part of a team working to improve lives globally through medical technology innovation. Manufacturing Engineer 1 or 2 performs and coordinates broad manufacturing engineering activities in the development and supply of capital and disposable medical devices and instruments. | 10/05/2025 |
| 415 | Abbott Sylmar, CA Software Engineer I Bachelors Degree in Computer Science, Engineering, Mathematics, or related field Exp: 0-2 years |
This Software Engineer I position is on the Digital Health Engineering team in Abbott’s Cardiac Rhythm Management division, and works on-site in Sylmar, California. The Digital Health Engineering team is responsible for developing, maintaining, and leveraging software solutions to provide internal and external stakeholders with the data and resources they need to effectively manage patient care, optimize clinical therapies, and improve product performance. Members of the Digital Health Engineering team are expected to translate complex customer and business needs into data-driven technical solutions. This role requires a blend of strong technical and software engineering skills, problem-solving abilities, customer centricity, as well as creativity, strong communication skills, and an entrepreneurial mindset. | 10/05/2025 |
| 416 | Abbott Temecula, CA Manufacturing Process Engineer Bachelor's Degree Exp: 1 year |
The Associate Manufacturing Engineer will serve as the primary manufacturing engineer supporting operations in Abbott Vascular Temecula. The individual performing this role will have to integrate with the team supporting the manufacturing line including but not limited to: the line supervisor, Quality Engineer and operators to address the opportunities found in their assigned manufacturing line. They will be accountable for quality, safety, product output and yield for their assigned manufacturing line. This person may also have a contributing role as a sustaining engineer for the department. | 10/05/2025 |
| 417 | Abbott Sturgis, MI Quality Engineer Master's Degree Exp: 1-3 years |
The Quality Engineer is responsible for developing and maintaining quality engineering methodologies and providing quality engineering support within new product development, manufacturing, or system/services support. | 10/05/2025 |
| 418 | Abbott Sylmar, CA Test Development Engineer I Bachelors Degree in Electrical engineering or related engineering field Exp: 6 months |
This Test Development Engineer I position works out of our Sylmar, CA location in the Cardiac Rhythm Managment Division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. Test Development Engineer assists with designing and developing non-product software and hardware to test new products. Test Development Engineer investigates and resolves production problems involving test equipment, software, and hardware. You will apply engineering and scientific principles to evaluate and solve technical problems. Remain abreast of and consults on technological advancements. Identify and routinely uses the most effective, cost-efficient, and best practices to execute processes; continually evaluates their effectiveness and appropriateness. | 10/05/2025 |
| 419 | Abbott Sylmar, CA Associate Supplier Quality Engineer Bachelors Degree in Engineering or Technical Field Exp: 0-2 years |
Identify and implement effective process control systems to support the development, qualification, and on-going manufacturing of products to meet or exceed internal and external requirements. Lead in the implementation of assurances, process controls, and CAPA systems designed to meet or exceed internal and external requirements. Assist in the development and execution of streamlined business systems which effectively identify and resolve quality issues. Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues. Design and conduct experiments for process optimization and/or improvement. Appropriately document experiment plans and results, including protocol writing and reports. Lead process control and monitoring of CTQ parameters and specifications. Lead and implement various product and process improvement methodologies (e.g., Six Sigma and Lean Manufacturing). Lead the investigation, resolution and prevention of product and process non-conformances. Participate in or lead teams in supporting quality disciplines, decisions, and practices (e.g., represent the Quality function as a Core Team Member). Lead in the completion and maintenance of risk analysis. Work with design engineering in the completion of product verification and validation. Work with microbiology to ensure appropriate environmental monitoring and that microbiology requirements are considered in product and process development activities. Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements. Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors. | 10/05/2025 |
| 420 | Abbott Alameda, CA Specialist Quality Assurance Bachelors Degree Exp: 1+ years |
The Specialist Quality Assurance Engineer will analyze quality standards for components, materials or services. You will apply measures, sampling methods, testing methodology and other procedures that ensure that quality standards are met. | 10/05/2025 |
| 421 | Abbott St. Paul, MN Supplier Quality Engineer Bachelors Degree Exp: 1-3 years |
Ability to effectively communicate, facilitate and organize project activities relating to ensuring supplier quality. Develops and manages project schedules to ensure deadlines are met. Serves as the primary Quality contact for suppliers and provides technical assistance to management for suppliers as requested. Works with supplier development engineering to performs on-site annual and critical component supplier audits to ensure compliance with Quality Systems procedures and CSI requirements. Generates audit reports and ensures supplier audit findings are tracked to timely and closure. Provides quality systems input to suppliers such as, but not limited to: statistical process control, gage R&R studies, and capability studies. Resolves supplier quality issues at incoming inspection and the production line. Provides project team leadership and conducts investigations relating to supplier quality issues. Completes non-conforming material reports (NCMR), supplier requests for change (SRC), supplier corrective action requests (SCARs) and monitors follow-up with assigned supplier base. Routinely reports on supplier performance per defined metrics to management and other team members. Represent Quality during audits and interface with FDA, ISO, or any external auditor. | 10/05/2025 |
| 422 | AbbVie Irvine, CA R&D Engineer II Master’s Degree in Industrial and Systems Engineering, Mechanical Engineering, Biomedical Engineering, or a related field Exp: 1 year |
Contribute to the development and launch of new drug/medical device combination products. Independently design, execute, and interpret novel engineering research and development. Generate and lead new engineering proposals. Investigate, identify, develop, and optimize new test methods and techniques and set and meet experimental timelines. Innovate and implement new experimental protocols. Act as a critical contributor to feasibility, development, and verification testing stages of product development through creation and release of new test methods, as well as design verification plans, protocols, records, and reports. Effectively organize and present scientific plans and data. Contribute to writing and conceptual framework of publications, presentations, and patents. Act as a resource or mentor for others. | 10/05/2025 |
| 423 | AbbVie South San Francisco, CA Associate Scientist II - Cell Line Development MS Exp: No exp |
The Cell Line Development Group in South San Francisco, CA is seeking an Associate Scientist II to join a talented and collaborative team developing CHO cell lines for GMP applications. In this laboratory position the candidate will perform hands-on CHO cell line development for pipeline assets and support the establishment of automation capabilities in the group to increase throughput. The successful candidate will contribute to the evaluation and implementation of an automated liquid handler for cell culture workflows. | 10/05/2025 |
| 424 | Abeona Therapeutics Cleveland, OH Quality Control Analyst I (QC Analytical) BS in biochemistry, biology, microbiology, molecular biology or other relevant discipline Exp: 1-3 years |
The Quality Control Analyst I performs routine laboratory activities in support of Good Manufacturing Practices (GMP) testing for Quality Control (QC). Testing includes qPCR, immunostaining, protein characterization and product specific analytical test methods. Interacts with employees internal and external to Quality Control. | 10/05/2025 |
| 425 | Abeona Therapeutics Cleveland, OH Specialist I, Quality Assurance - Quality Operations Bachelor's degree in related field Exp: 1 year |
The Specialist I, Quality Assurance performs routine activities associated with manufacturing of cell and gene therapy products at the Abeona Therapeutics Inc. site in Cleveland, OH. This position supports the maintenance of the quality systems in support of a cGMP Operation for Manufacturing logistics processes relating to Abeona Manufactured Media batch record review and release from start to end of manufacturing activities, in-process sampling / testing, autoclave, and document management ensuring procedural and regulatory compliance throughout the manufacturing process. The Specialist I, Quality Assurance will report to the Associate Manager, Quality Assurance or above and will support manufacturing and quality control as the production area Quality Assurance representative. | 10/05/2025 |
| 426 | AstraZeneca Frederick, MD Specialist I Quality Control BS degree Exp: 0-5 years |
In this role, you will perform selected analytical quality control testing activities, including HPLC, GC, and UPLC testing. You will be responsible for conducting in-process and finished product testing according to standard operating procedures. Your duties will include completing documentation supporting testing procedures, maintaining lab instrumentation, and ensuring supply levels are adequate. You will read, understand, and follow SOPs while complying with cGMPs. Critical thinking and problem-solving will be key as you apply knowledge of good manufacturing and laboratory practices daily. Safety is paramount, and you'll adhere to company safety procedures and guidelines. Depending on your demonstrated ability, you may assist in executing protocols and laboratory studies required to support QC investigations, method validation, and stability studies. | 10/05/2025 |
| 427 | AstraZeneca Gaithersburg, MD Scientist, Oncology TCR-T Cell Therapy Master’s degree in Immunology, Cancer Biology, Cell Biology, or relevant scientific field Exp: 1 year |
We are seeking a highly motivated and independent Scientist to join our rapidly growing Cell Therapy Team. In this role, you will contribute to advancing innovative Cell Therapy products by designing and conducting laboratory experiments, developing methodology, and generating and interpreting scientific data in a highly collaborative environment.Expertise inin vitro and in vivo studies and T cell biology is critical for this role. To be successful in this role, you must be well-organized and keep an excellent written record of your work. You will be based in Gaithersburg, MD and report to the Associate Director, TCR-T Cell Therapy. | 10/05/2025 |
| 428 | Adare Vandalia, OH Analytical Scientist Master’s Degree in Chemistry or related discipline Exp: 0-1 years |
The Analytical Scientist will support the development and validation of analytical methods for raw materials, work-in-process, and finished products to provide testing support for the formulation development and clinical supplies release process. The Scientist will also be expected to provide some training, coaching, and mentoring for more junior scientists. | 10/05/2025 |
| 429 | Adicet Bio Redwood City, CA Manufacturing Associate 2 – Cell Therapy Bachelor’s degree in biological sciences, engineering, or related discipline Exp: 1-2 years |
We are seeking a highly motivated and detail-oriented individual with a strong background in cell process development and/or manufacturing. The Manufacturing Associate II will report to the Director of Manufacturing and play a key role in supporting daily GMP manufacturing operations for allogeneic CAR T cell therapies. | 10/05/2025 |
| 430 | ADMA Biologics Boca Raton, FL QA Specialist I - Manufacturing Oversight Bachelor's Degree Exp: 1-3 years |
The QA Specialist I - Manufacturing Oversight performs manufacturing oversight activities to ensure compliance with policies and procedures. Oversight activities include, but are not limited to, real-time manufacturing batch record review, review of manufacturing documentation (logs, charts, etc.), and resolution of issues on the manufacturing floor. | 10/05/2025 |
| 431 | ADMA Biologics Boca Raton, FL Microbiologist I, Quality Control B.S. in Biological Science or related science discipline Exp: 0-3 years |
Perform environmental monitoring and water sampling within the controlled manufacturing areas and QC Laboratory. | 10/05/2025 |
| 432 | Agilent Newport, DE Capital Projects Engineer Bachelor’s degree in Mechanical, Electrical, or Chemical Engineering Exp: 1+ years |
Join a team that’s advancing innovation in life sciences. At Agilent, we empower our engineers to drive impactful change through smart design, efficient processes, and collaborative problem-solving. We’re looking for a Manufacturing Engineer to support our LC Column Manufacturing operations, with a focus on capital project execution, equipment optimization, and continuous improvement. | 10/05/2025 |
| 433 | Agilent Remote, CA Field Service Engineer - Pathology Bachelor’s or Master’s degree in a scientific field (e.g., Chemistry, Biochemistry, Biotechnology, Analytical Chemistry) Exp: 1+ years |
Join Agilent as a Field Service Engineer – Pathology and play a critical role in supporting scientists and healthcare professionals in delivering life-enhancing discoveries. In this dynamic role, you will provide on-site technical support, ensuring the optimal performance of Agilent’s pathology solutions. Your expertise will directly impact laboratories by minimizing downtime, optimizing efficiency, and enhancing customer success. | 10/05/2025 |
| 434 | Agilent Boulder, CO Manufacturing Associate 2 – Cell Therapy Bachelor’s or Master’s Degree Exp: 0-1+ years |
As a Manufacturing Associate, you will check and schedule resources to ensure on-time delivery. Your scientific knowledge and background will be leveraged through your review of formulation documents and active ingredient dilution to ensure that products are manufactured to specification. Responsible for performing a variety of support duties in one or more manufacturing areas. Duties may be related to cleaning, ordering, stocking, preparing, installing, maintaining, repairing and supporting manufacturing equipment and processes, Assistance with validation protocol execution, product test and troubleshooting, and technical analyses and problem-solving, Performs daily cleaning activities and maintains production areas in an audit ready, neat, clean and orderly state. You will have an opportunity to become skilled in the use of a wide range of lab instruments which are essential to meeting our customers' requirements. Having the ability to learn quickly on the job, anticipate and resolve potential manufacturing and delivery issues and maintaining the highest level of quality are critical. | 10/05/2025 |
| 435 | Agilent Los Angeles, CA Field Service Engineer - GC/GCMS Bachelor's or Master's Degree within the science field Exp: 1+ years |
As a Field Service Engineer for Agilent, you will work at a variety of labs, so having an appetite for continuously learning about new instruments, software and consumables is key. Applying your communication skills, creativity and can-do attitude is essential. The ability to help with solving customer problems and a commitment to deliver the highest levels of customer service is how you will build customer success. | 10/05/2025 |
| 436 | Agilent Frederick, CO Validation Engineer Bachelor’s or Master’s degree Exp: 1-2+ years |
Performs cleaning validation and equipment commissioning and validation engineering duties to support initial start-up and qualification of a new Active Pharmaceutical Ingredient (API) manufacturing facility at Agilent Technologies Nucleic Acid Solutions Division in Frederick, Colorado. Primary responsibilities include the execution, reporting, and communication of validation activities compliant with pharmaceutical Good Manufacturing Practices (GMP). | 10/05/2025 |
| 437 | Agilent Carpinteria, CA Engineer - Manufacturing Systems (MES) Bachelor’s or Master’s degree or equivalent experience in Engineering Exp: 1+ years |
Join Agilent’s innovative manufacturing team and help craft the future of smart, compliant, and efficient production systems. As a Manufacturing Systems Engineer, you’ll chip in to the development and optimization of digital manufacturing solutions, ensuring flawless integration of software, equipment, and processes across regulated environments. | 10/05/2025 |
| 438 | Forge Biologics Columbus, OH Analytical Quality Control, Analyst I (2nd Shift) Bachelor’s degree in biology, molecular biology, virology, biochemistry or related discipline Exp: 0-4 years |
We are currently seeking a Quality Control (QC) Analyst I, Analytical Testing, to join the Forge Biologics team. This role will perform characterization and release testing QC for AAV vectors, plasmids, and cell banks, while maintaining meticulous records and ensuring the accuracy of data for all products. This position is responsible for routine test method execution, assisting in method qualification and validation, instrumentation troubleshooting, and data analysis. The ideal candidate will be skilled in technical problem-solving and laboratory techniques to support our growth in the Gene Therapy sector. The Analyst I role offers an excellent opportunity to gain hands-on experience in the field of gene therapy. | 10/05/2025 |
| 439 | Forge Biologics Columbus, OH Lab Coordinator Bachelor's degree in scientific discipline (Biology, Chemistry, or related field) Exp: 1-3 years |
The Laboratory Coordinator, QC Analytical Testing is responsible for day-to-day coordination of laboratory operations to ensure that QC spaces are well-maintained, and compliant with GMP expectations. Key responsibilities include oversight of laboratory cleaning and 5S activities, support for equipment calibration and preventive maintenance (PM), pipette verifications, and sample shipment for external testing. This role will work closely with the Laboratory Manager and QC staff to support smooth laboratory operations and execution of GMP testing. | 10/05/2025 |
| 440 | Alamar Fremont, CA Associate Scientist II – Technology Access Program Master’s degree in Immunology, Neuroscience, Biochemistry, or a related discipline Exp: 1-2 years |
We seek a highly motivated Associate Scientist to join a dynamic team of professionals in the Technology Access team to support our company mission. In this role, you will work cross-functionally across multiple teams including R&D, Sales and Marketing to design, execute and deliver NULISA immunoassay collaboration projects as part of the Technology Access Program. An ideal candidate will have a background in proteomics and bring hands-on experience in sequencing workflows, NGS library preparation, and automated liquid handling instruments. The ability to manage multiple projects in a fast-paced, collaborative environment is highly preferred. | 10/05/2025 |
| 441 | Alcami Morrisville, NC Scientist II - Compendial Testing, Raw Materials Masters degree in Chemistry, Biochemistry, or related field Exp: 0+ years |
The Scientist II (Chemistry) is accountable for driving results in a fast-paced environment by performing analytical routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. For this Scientist II (Chemistry) position, TOC, UV, osmolality, density, titration and pH are commonly employed in the described testing in addition to other key methodologies such as KF, CCIT and HPLC. Test methods employed may be compendial (i.e. USP, EP, JP) or proprietary (client supplied or developed by The Company) and may also assist with method verification / method validation projects as needed. | 10/05/2025 |
| 442 | Alcami Morrisville, NC Quality Specialist - GMP Master’s degree in Chemistry, Biology, or relevant field Exp: 1+ years |
The Quality Specialist will provide site quality support in a fast-paced environment by effectively performing activities of substantial variety to ensure quality and compliance with applicable regulatory requirements and is proficient in all document and protocol approvals applicable to the respective processes executed at the respective lab or manufacturing facility. These activities include reviewing documents and data, supporting audits and inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance training as needed. The Quality Specialist serves as quality host for client and regulatory agency audits and inspections. The position develops SOPs or other quality documents as needed. | 10/05/2025 |
| 443 | Shimadzu Virtual, NJ Field Service Technician I AA EE or similar, BS preferred Exp: 1 yr |
Provide daily repair and maintenance support for assigned products, including installations; Conduct in-house bench repairs and onsite customer repairs as needed while primarily handling field service calls with limited supervision; Travel within the local region (including day and overnight trips) to support customer needs; Offer technical support via phone to customers and field personnel regarding repairs, maintenance and installations. | 10/01/2025 |
| 444 | Spear Bio Woburn, MA Associate Scientist/Senior Associate Scientist, Assay Development MS in Biology, Biochemistry, Biomedical Engineering or a related discipline Exp: 1-2+ years |
We are seeking a highly motivated and experienced Associate Scientist/Senior Associate Scientist to join our Assay Development team, with hands-on experience in developing and validating ultrasensitive immunoassays. The ideal candidate will support the full lifecycle of assay development, from initial concept and research to validation and assay transfer. This individual will play a pivotal role in advancing Spear Bio’s new range of ultrasensitive immunoassays and assay biomarker programs. This role is based onsite in our lab in Woburn, MA 5 days/week. | 09/29/2025 |
| 445 | SRI Palo Alto, CA Mechanical Engineer Bachelors in Mechanical Engineering or a related field Exp: 1+ years |
The Bright Ceramics Technology group (BCT) is focused on developing, applying, and commercializing a unique technology platform based upon advanced materials. They develop and manufacture cutting-edge components and systems. BCT is currently searching for new grad Mechanical Engineers to join their team. The ideal candidates will be able to perform basic engineering analysis, complete detailed specifications, and be able to build and troubleshoot systems with minimal supervision. Working with interdisciplinary teams, the ME will apply their knowledge of mechanical design and materials properties to invent, fabricate, and test complex components and systems that are benchmarks of elegant and effective design. Successful applicants will be proficient in mechanical design and analysis, prototyping, a wide range of manufacturing processes, electro-mechanical systems, 3D CAD, and system fabrication. | 09/29/2025 |
| 446 | Stallergenes Greer Lenoir, NC Validation Engineer Bachelors degree in a scientific field Exp: 1-2 years |
Independently plan, perform and/or coordinate validation projects to ensure timely completion. Draft and coordinate execution of process validation and equipment qualifications (IQ, OQ, PQ, FAT’s, SAT’s). Draft/or provide technical guidance for SOPs and other master documents. Remain current with industry and regulatory agency trends. Keep Tech Ops Management informed of the status of validation activities and projects. Support Engineering and Operations in the development of critical process parameters. Provide technical leadership for deviation investigations. Analyze data and provide recommendations for improvements in manufacturing process, and equipment. Prepare and execute protocols, Engineering Studies, and other technical documents, and participate in the interpretation of data, collaborating with other departments. Own and Execute Audit Role as the Support / Research SME collecting data to support Audit Requests for the Validation/Calibration Department for all areas of validation. Other responsibilities as directed. Conduct peer-review of protocols and reports. Position may require occasional travel and working with validation consultants and the validation team located at the North Carolina site | 09/29/2025 |
| 447 | Stallergenes Greer Lenoir, NC Chemist I Bachelor degree in Science /preferably in Chemistry Exp: 0-2 years |
Analysis of allergenic extracts by Elisa, RID and IEF. Analysis of preservatives phenol and glycerin by HPLC. Wet chemistry analysis specific gravity, identifications, USP and EP compendia and WFI analysis. Operates laboratory instrumentation as FTIR, GC, HPLC and others | 09/29/2025 |
| 448 | Steris Cooper City, FL Quality Engineer BS Engineering in related technical field Exp: 1+ years |
The Quality Engineer in our Cooper City, Florida facility is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. As a Quality Engineer, you will support complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 09/29/2025 |
| 449 | Steris Whippany, NJ Quality Analyst Bachelor’s degree in Scientific or Technical Field Exp: 1 year |
The Quality Analyst in the STERIS Applied Sterilization Technologies (AST) Whippany, New Jersey location is responsible for assisting in administration of the quality management system to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. The Quality Analyst leads complaint/CAPA investigations, supplier quality improvement initiatives, continuous improvement initiatives and countermeasures with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 09/29/2025 |
| 450 | Sterling Pharma Solutions Germantown, WI Analytical R&D Associate Scientist Master’s degree in a scientific discipline such as analytical chemistry, or related field Exp: 0-2 years |
As the Analytical R&D Associate Scientist, you are accountable for driving results by supporting manufacturing activities through phase specific method development and method validation activities. The Analytical Scientist will execute the development of analytical methods and improve existing methods to support our active pharmaceutical ingredients development program. The Associate Scientist II works closely with a multifunctional team to support quality control and chemical research and development groups. | 09/29/2025 |
| 451 | Sterling Pharma Solutions Germantown, WI Analytical Chemist Bachelors Degree in Chemistry or related field Exp: 0-2 years |
As the Analytical Chemist at Sterling, you will be accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of active pharmaceutical ingredients development or pharmaceutical manufacturing. Testing performed directly supports manufacturing through the release of raw materials, intermediates and API’s; as well as in-process controls, equipment cleaning verification, reference standard qualification, and stability program. The Analytical Chemist will develop the ability to efficiently organize the routine work with minimum supervision and to properly evaluate and interpret generated data working. | 09/29/2025 |
| 452 | Sterling Pharma Solutions Germantown, WI Associate Scientist Bachelor’s degree in Chemistry or related field Exp: 0-2 years |
The Associate Scientist, under the direction of a senior scientist, executes chemical reactions on a gram to multi-kilogram scale and performs routine analytical procedures to monitor reaction progress. This role requires the incumbent to efficiently organize routine work with supervision and properly evaluate and interpret generated data. The Associate Scientist will exercise judgment within defined procedures and practices to determine appropriate action. The position requires superior leadership behaviors of the Sterling core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 09/29/2025 |
| 453 | Stryker Portage, MI Electrical Design Engineer, R&D Bachelor's degree in EE or related discipline Exp: 0+ years |
Are you a passionate electrical engineer with a desire to innovate and shape the future of healthcare? Join our forward-thinking medical device team in our Surgical Technologies business unit, working specifically on developing our Next Generation Neptune portfolio, where your work will directly impact patient outcomes. As a key contributor, you will independently design and develop advanced electrical components and sub-systems for groundbreaking medical devices, using cutting-edge techniques in circuit design, testing, and problem-solving. | 09/29/2025 |
| 454 | Supernus Pharmaceuticals Rockville, MD Chemist Analytical Sciences PA Bachelor’s degree in life sciences (Chemistry degree is preferred) Exp: 0+ years |
The Chemist Analytical Sciences PA will provide analytical support for pharmaceutical solid dosage forms primarily by using dissolution testing, spectroscopy, HPLC, wet chemistry, including maintaining proper documentation. | 09/29/2025 |
| 455 | Syner-G BioPharma Group Worcester, MA Project Engineer Bachelor’s or advanced degree (e.g., B.S., M.S.) in Mechanical, Electrical, Civil Engineering, Facilities Engineering, or related discipline Exp: 1-5 years |
The Project Engineer is responsible for the strategic oversight and hands-on management of building systems, infrastructure projects, and utility operations across the organization. This role ensures optimal performance, safety, and compliance of all facilities-related functions, including HVAC, electrical, plumbing, and environmental systems. The Engineer will lead cross-functional initiatives, manage capital projects, and serve as a technical expert in building operations, cleanroom design, and sustainability efforts. The ideal candidate operates independently and proactively, driving continuous improvement and operational excellence. | 09/29/2025 |
| 456 | Syner-G BioPharma Group Norwood, MA Sr. Project Engineer Bachelor’s or advanced degree (e.g., B.S., M.S.) in Mechanical, Electrical, Civil Engineering, Facilities Engineering, or related discipline Exp: 1-5 years |
The Sr. Project Engineer is responsible for the strategic oversight and hands-on management of building systems, infrastructure projects, and utility operations across the organization. This role ensures optimal performance, safety, and compliance of all facilities-related functions, including HVAC, electrical, plumbing, and environmental systems. The Engineer will lead cross-functional initiatives, manage capital projects, and serve as a technical expert in building operations, cleanroom design, and sustainability efforts. The ideal candidate operates independently and proactively, driving continuous improvement and operational excellence. | 09/29/2025 |
| 457 | Syner-G BioPharma Group Boston, MA Associate Facilities Engineer Bachelor’s degree in a related field Exp: 0-2 years |
We are seeking a Facilities Engineer with experience in the management, execution, and day-to-day support of building and plant operations, including labs, manufacturing plants, utilities, equipment, and systems. The ideal candidate will perform routine inspections, maintain documented records, and be on-call for emergencies, ensuring compliance with regulatory requirements and GMPs. Effective communication and collaboration with various departments are essential to meet the facility’s needs and quickly resolve any issues. | 09/29/2025 |
| 458 | Syner-G BioPharma Group West Warwick, RI Project Engineer (1st & 2nd Shift) Bachelor’s or advanced degree (e.g., B.S., M.S.) in Mechanical, Electrical, Civil Engineering, Facilities Engineering, or related discipline Exp: 1-5 years |
The Project Engineer is responsible for the strategic oversight and hands-on management of building systems, infrastructure projects, and utility operations across the organization. This role ensures optimal performance, safety, and compliance of all facilities-related functions, including HVAC, electrical, plumbing, and environmental systems. The Engineer will lead cross-functional initiatives, manage capital projects, and serve as a technical expert in building operations, cleanroom design, and sustainability efforts. The ideal candidate operates independently and proactively, driving continuous improvement and operational excellence. | 09/29/2025 |
| 459 | SystImmune Redmond, WA Research Associate/Senior Research Associate BS or MS in immunology, biochemistry, molecular biology, structural biology, or a related field Exp: 1+ years |
We are seeking a skilled Research Associate/Senior Research Associate with experience in utilizing display technologies (yeast/phage) in protein engineering, directed evolution, or binder discovery. This is a laboratory-based role that will be supporting protein engineering efforts in discovering novel binders and novel protein leads/scaffolds. The position will join a growing protein engineering team in an innovative organization and reports to the Director of Protein Engineering. The ideal candidate will be a quick learner with a broad experience set with direct expertise in a display technology and/or an adjacent field including but not limited to high throughput molecular biology, antibody/binder discovery, and protein engineering. Industry experience in biologics drug development is required. | 09/29/2025 |
| 460 | SystImmune Redmond, WA Research Associate/Senior Research Associate - Cell Science Bachelor’s degree in biology or a related science major Exp: 1+ years |
Located in Redmond WA, Systimmune Inc.is a bio-pharmaceutical company focused on the treatment of cancer through developing novel therapeutic multi-specific antibodies, as well as antibody-drug conjugates (ADCs). Our objective is to create biologics that work through systematic intervention on the solid tumor micro-environment, to either directly attack the tumor and/or to activate the immune system to attack the tumor. We are seeking a Research Associate / Senior Research Associate with experience in cell culture and plasmid preparation to join our Cell Science Department. | 09/29/2025 |
| 461 | Takeda Social Circle, GA Engineer I Bachelor’s degree in Engineering or a related field Exp: 1 year |
Join Takeda as an Engineer I where you will provide process support to the Fractionation manufacturing group by solving technical issues within the Social Circle Fractionation manufacturing facility. You will assist your quality and manufacturing partners in maintaining process compliance, aiding in the implementation of yield and process improvements, and supporting process validation activities. As part of the Fractionation Manufacturing Sciences team, you will report to the Associate Director of Manufacturing Sciences, Fractionation. | 09/29/2025 |
| 462 | Tanvex Biopharma San Diego, CA Manufacturing Technician I, Production Support Bachelor's degree in EE or related discipline Exp: 0-3 years |
Under supervision, the Manufacturing Technician, Production Support, will perform routine manufacturing activities in GMP manufacturing areas, solution preparation, dispensing raw material, bioprocessing support and autoclave operation. Operations will be performed according to Standard Operating Procedures (SOP), Work Instructions (WI) and Master Batch Records (MBR). Perform manufacturing steps, execute routine MBRs, and revise documents such as MBRs and SOPs as needed. Flexible shift schedules and overtime may be required. | 09/29/2025 |
| 463 | TE Connectivity Middletown, PA Quality & Reliability Engineer I Masters degree in Industrial or Mechanical engineering Exp: 1-2 years |
Interact with cross functional team members to plan product development activities in support of project requirements and customer needs. Participate in all activities impacting customer requirements including DFMEA, Design Reviews, and Design for Manufacturing Reviews. Take hands on personally committed approach to the Quality feedback loop including resolving customer complaints and plant issues plus line concerns. Participate in development of PFMEA. Responsible for development of Control Plans/Inspection Plans, First Article Inspection and Capability Study planning and acceptance for new or revised tooling, PPAP or other customer required documentation. Create, and Safe Launch plans to help ensure that all production risks are addressed throughout the Project lifecycle. Support all activities relating to the refinement/improvement and creation of process from a quality perspective. Management of internal and external suppliers from a quality perspective. Perform failure analysis using 8D format to clearly define the problems, scope, root cause and corrective actions. Interface with supplier quality engineering as needed to coordinate actions related to supplier process design, inspection and non-conforming materials. Travel as required to ensure project success. This position will have global responsibilities requiring flexible working. Employee must perform his/her job within acceptable safety, environmental, quality, productivity and performance standards as outlined in local and global policies and handbooks. Transmission of customer specific requirements and Quality Manuals into the Project/Product. Risk estimation and mitigation through Project lifecycle using clearly defined and constantly improved measurables including escalation as required. | 09/29/2025 |
| 464 | TE Connectivity Northborough, MA EH&S Analyst II BA/BS Degree in, Environmental Engineering, Environmental Studies , Industrial Engineering or related major Exp: 1-3 years |
Assists in ensuring and monitoring safety in the workplace including the application and communication of health, safety and hazardous material standards, procedures and practices consistent with established company, environmental and government regulations | 09/29/2025 |
| 465 | Tempus Chicago, IL Molecular Technologist I (Extractions) BS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 0-1+ years |
Work with a cutting-edge genomics workflow to provide high-quality data with rapid turnaround times in a clinical laboratory. Perform routine testing, quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform nucleic acid extraction and DNA/RNA quantification and qualification using robotics and automated liquid handlers. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Obtain 12 continuing education hours in the field of oncology or molecular biology. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 09/29/2025 |
| 466 | Tempus Research Triangle Park, NC Quality Control Technologist I-III BS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work within a cutting-edge genomics workflow to provide equipment quality control support in a high-volume clinical molecular laboratory. Help create and implement new equipment functionality for use by Tempus R&D and clinical lab staff while maintaining CLIA/CAP/ISO compliance. Complete Performance Qualifications (PQs), Preventive Maintenance (PM), relocation, and routine maintenance for all clinically approved molecular laboratory equipment. Collect and help analyze metrics. Investigate equipment related issues and help facilitate and implement corrective and preventative actions. Interact with lab management and personnel to provide training, troubleshoot issues, and prioritize QC tasks. Report significant findings/deviations and system deficiencies to lab management, as appropriate. Update SOPs and equipment records within the document control system, including creation/ revision/ review of internal SOPs and other quality documentation. Create and review protocols and qualification summaries. Support the Lab Facilities team with freezer defrosts and hazardous waste pick-up as needed. Monitor and respond to laboratory temperature excursions. | 09/29/2025 |
| 467 | Ritedose Columbia, SC Microbiologist II BS degree in Microbiology or related field Exp: 1 year |
The Microbiologist II is responsible for all duties related to performing environmental monitoring, personnel monitoring, microbial enumeration, microbial identification, and sampling of utilities. The Microbiologist I is also responsible for performing all the microbiological testing related to raw materials, utilities, and in-process product testing. Other responsibilities include data entry, data review, ensuring calibration of equipment, maintaining inventory of laboratory supplies, and maintaining the Microbiology laboratory by ensuring its cleanliness and order. | 09/29/2025 |
| 468 | Ritedose Columbia, SC Process Development Engineer BS degree in Chemical or Mechanical Engineering Exp: 1-3 years |
Process Development Engineer for Finished Packaging is responsible for designing and implementing Finished Packaging development for development products. The Engineer will design and implement appropriate change requests, packing studies, batch records, forms, procedures, work instructions, risk assessments, etc. as needed to achieve the development and production goals of the organization. The Engineer’s responsibility will include supporting other Formulation, Filling, Bulk Packaging development as assigned by management. | 09/29/2025 |
| 469 | Thermo Fisher Scientific Greenville, NC Formulation Technician II Bachelor's degree Exp: No exp |
As a Formulation Technician II, you will play a vital role in producing sterile injectables and working on moderate-scale problems that require analysis and critical thinking. You will follow written and verbal instructions to ensure that pharmaceutical products are manufactured in accordance with industry guidelines and regulations. | 09/29/2025 |
| 470 | Thermo Fisher Scientific Plainville, MA Technical Operations, Technical Writer II Bachelor’s degree Exp: 1-2 years |
As RSO, you’ll play a key role in supporting our GMP manufacturing operations by developing and maintaining high-quality documentation. Your work directly impacts the consistency, safety, and compliance of the treatments we help bring to market. | 09/29/2025 |
| 471 | Thermo Fisher Scientific Greenville, NC R&D Mfg Scientist II - Analytical Development Masters Degree in Chemistry, Biochemistry, Molecular Biology, or related physical/biological science field Exp: 1+ years |
Provides routine analyses in a biochemistry environment within defined procedures and practices. Performs analytical methods for moderately sophisticated testing on samples, stability, and production intermediates to support process development and/or manufacturing operations. May research and implement new methods and technologies to improve operations. Makes detailed observations and reviews, documents, and communicates test results. | 09/29/2025 |
| 472 | Thermo Fisher Scientific Wilmington, DE Associate Scientist, Purification Process Science BS degree in biochemistry, bioengineering, biology, chemistry or related fields Exp: 0-1+ years |
Our client is seeking a motivated and dedicated protein purification scientist to support protein purification process development and optimization primarily for novel therapeutic monoclonal antibody products including bispecifics throughout all stages of clinical trials. | 09/29/2025 |
| 473 | Thermo Fisher Scientific Greenville, NC QC Scientist I Bachelor’s degree in a biology/related field Exp: 1+ years |
A successful person will perform Environmental Monitoring tasks in support of Steriles production within classified areas. The individual is encouraged to follow the 4i Values that are held in high regards by the company when completing their work. The four values are integrity, innovation, intensity, and involvement. The job function includes aseptic technique which requires the individual to gain knowledge of aseptic gowning as well as working in cleanrooms in order to monitor the area while sterile products are filled and manufactured. | 09/29/2025 |
| 474 | Thermo Fisher Scientific Boston, MA Labs FSP Scientist - GMP, Chemistry Master's degree in a scientific discipline Exp: 0-2 years |
As a Scientist, you provide technical support for Release and Stability Laboratory (RSL) department supporting method validations, investigations, reference standard and external testing. Specific assigned persons are responsible to ensure activities occur in an efficient and cGMP compliant manner while fostering the customer's vision and values. | 09/29/2025 |
| 475 | Thermo Fisher Scientific Greenville, NC QC Scientist I, QC Steriles Bachelor’s degree in life science, preferably in Chemistry Exp: 1 year |
Perform analyses in a chemistry environment within defined procedures and practices. Perform analytical methods for moderately to complex testing on a variety of cleaning, in process, stability, and release samples. Support internal manufacturing operations. Make detailed observations and review, documents and communicate test results; recommend solutions. | 09/29/2025 |
| 476 | Transpire Bio Sunrise, FL Pharmaceutical Manufacturing Process Associate Scientist I/II BS or MS Degree in Chemical/Biochemical Engineering, Chemistry, Biochemistry or a related scientific discipline Exp: 0-5 years |
In this role, the Process Associate Scientist I/II will involve developing and optimizing pharmaceutical manufacturing processes, ensuring product quality and consistency, and complying with regulatory requirements on commercial formulations for orally inhaled and nasal drug products (OINDPs). Conducts pilot scale manufacturing activities including formulation and manufacturing process development, manufacturing process scale-up and process transfer activities across equipment, manufacturing scales and sites. The individual will design and execute formulation experiments, organize and analyze results with minimal supervision, and communicate data and interpretation to product development team. Contribute towards the development of orally inhaled and nasal drug products (OINDPs) by following regulatory guidelines, industry best practices, US FDA cGMPs, and other relevant guidelines. | 09/29/2025 |
| 477 | Tri-Pac South Bend, IN Lab Technician Bachelor’s degree in a scientific field Exp: 1-2 years |
The Lab Technician performs chemical analysis and testing on chemical raw materials and in-process/finished batches according to methods and specifications as defined by the customer. He/she assists with compiling, analyzing and interpretation of results as well as maintaining the flow of samples and paperwork through the laboratory. The Lab Technician maintains laboratory equipment and instrumentation to ensure ideal usage and has a strong attention to detail. The Lab Technician is able to effectively correspond with internal customers, has excellent organizational skills, able to perform physically demanding work such as moving and lifting equipment and capable of standing for long periods of time. | 09/29/2025 |
| 478 | Twist Bioscience Quincy, MA Research Associate II, Antibody Characterization Master’s degree in molecular biology, biochemistry, or a related discipline Exp: No exp |
We are seeking a motivated individual to join our team and expand our antibody characterization department. Using state-of-the-art technologies and workflows, this Research Associate would work with the Antibody Characterization team to ensure project-specific deliverables are met across a diverse panel of discovery campaigns and contract services. The role would involve wet lab experimental design, execution, and data analysis for multiple custom antibody development projects incorporating various biologics assay formats. | 09/29/2025 |
| 479 | Twist Bioscience Quincy, MA Research Associate II, Protein Analytics Master’s degree in molecular biology, biochemistry, or a related discipline Exp: No exp |
We are seeking a motivated individual to join our team and expand our bioanalytical department. Using state-of-the-art technologies and workflows, this Research Associate would work with the Protein Analytics team to ensure project-specific deliverables are met across a diverse panel of discovery campaigns and contract services. The role would involve wet lab experimental design, execution, and data analysis for multiple custom antibody development projects incorporating various biologics assay formats. | 09/29/2025 |
| 480 | Twist Bioscience South San Francisco, CA Research Associate II - R&D M.S. in Molecular Biology, Biochemistry, Chemistry or a closely-related field Exp: 1-2 years |
As Research Associate II, you will work on new product development and existing process improvement. Your work will be mainly at the bench, however, you will have the opportunity to use high-throughput robotic instruments as well as bioinformatics tools to expand your expertise. You will work alongside and learn from some of the best scientists and bioinformaticians in the business. | 09/29/2025 |
| 481 | Unither Pharmaceuticals Rochester, NY Laboratory Application Scientist Master’s degree in life science such as Biology, Pharma Sciences, Analytical Sciences, or closely related discipline Exp: 1-3 years |
The Laboratory Application Scientist ensures that all laboratory systems composed of equipment, instruments and computerized systems are properly maintained, qualified, calibrated and secured to be properly used by the laboratory users to ensure a high level of confidence with product results. Provide access management for each computer system, while ensuring data handling and data integrity meet internal SOP and FDA requirements. This position is partnered with the laboratory system owners and the IT group. Ensuring all laboratory systems are properly used in chemistry and microbiology laboratories and assisting laboratory staff with technical issues and training. Provides recommendations on efficiency, new technology and best practices in the QC laboratories. | 09/29/2025 |
| 482 | Vantage MedTech Lenexa, KS NPI Engineer BS or MS degree in Engineering, preferably Mechanical or Manufacturing Engineering Exp: 1-3 years |
The NPI (New Product Introduction) Engineer will be responsible for ensuring that our innovative designs are transitioned into effective and sustainable production. Our life saving products are manufactured in Kansas City and require predictable delivery of high quality, cost-effective production over 5+ year product lifetimes. You will collaborate with Vantage MedTech’s Engineering and Manufacturing teams to provide input on the device design’s manufacturability, and plan and execute the transfer of these new products to our manufacturing facility. You will be responsible for ensuring that robust manufacturing processes are created, updated and in compliance with company standards, ISO, and GMP as required. In addition, you will help drive improvement projects that impact quality and productivity. | 09/29/2025 |
| 483 | Vantage MedTech Lenexa, KS Design Quality Engineer Bachelor's degree in Engineering Exp: 1-3 years |
Vantage MedTech is seeking a Design Quality Engineer to serve as the cornerstone of Quality Assurance in cutting-edge design projects, ensuring they meet the highest standards of excellence and compliance. This role is responsible for maintaining alignment with the Vantage MedTech Quality Management System and design control processes, acting as the QA representative on assigned projects. This individual will enhance the capabilities of the design engineering team by overseeing the maintenance and compliance of the Design History File (DHF), Device Master Record (DMR), and document control processes, while upholding compliance assurance for external partners. | 09/29/2025 |
| 484 | RayzeBio Indianapolis, IN Operator – Isotope Production Bachelor's in a STEM Field Exp: 1-4 years |
The Operator – Isotope Production will be an integral part of bringing RayzeBio’s innovative drug products to patients in need. As Operator – Isotope Production, you will be instrumental in implementing a novel isotope production program that will manufacture the clinical and commercial scale radioisotopes for RayzeBio’s drug products. This individual will be part of a team responsible for producing RayzeBio’s radioisotopes under Good Manufacturing Practices (GMP). Additionally, you will be the front line in ensuring compliance with radiation safety requirements on the production floor. The Operator – Isotope Production will report directly to the operations leader of Isotope Production. Operator level will be evaluated with experience and qualifications. | 09/22/2025 |
| 485 | Reckitt Montevale, NJ R&D Assistant, Germ Protection - Lysol Aerosols BS/BA degree in a related science Exp: 0-2 years |
The R&D Assistant will work with technical product development on key projects for the R&D team. | 09/22/2025 |
| 486 | Regeneron Tarrytown, NY Associate Scientist - Formulations (Drug Product Development) BS or MS in Pharmaceutical Sciences, Biomedical Engineering, Chemical Engineering, Biochemistry, Chemistry, Biophysics or a related field Exp: 0-4 years |
Regeneron's Formulation Development Group, in Tarrytown NY is looking for an energetic Associate Scientist. In this exciting role, you support drug product development activities from candidate selection and pre-clinical development through clinical development and commercialization for a variety of drug modalities which may include mAb, ADC, siRNA, AAV, LNP in a variety of drug and delivery presentations for liquid and lyophilized DP, and novel drug delivery technologies. | 09/22/2025 |
| 487 | Regeneron Tarrytown, NY Associate Scientist - Bioassay Development BS/MS Exp: 0-2+ years |
We are seeking an experienced and motivated Associate Scientist to join the Bioassay team as a part of our Therapeutic Proteins Department. Our group’s focus is to develop assays to interrogate regulation of molecular function and signaling which contributes to the therapeutic mechanism of action and we play an integral role in discovery and characterization of therapeutic molecules across diverse disease areas. You will develop cell-based functional assays to identify and characterize therapeutic antibodies. We hope you are excited to work collaboratively across functions to meet project achievements, with the goal to deliver therapies that transform the lives of patients. | 09/22/2025 |
| 488 | Regeneron Tarrytown, NY Associate Scientist - Protein Development BS or MS in biology, molecular biology, protein chemistry, engineering chemistry, or a related field Exp: 1-3 years |
We are seeking an Associate Scientist to join Reagent group within our Therapeutic Proteins department. You will join our ongoing efforts to purify and biochemical characterize of protein reagents. | 09/22/2025 |
| 489 | Regeneron East Greenbush, NY Associate Design Quality Engineer (Medical Device) Bachelor’s degree in an Engineering subject area Exp: 0-2 years |
We are currently looking to fill a Medical Device Quality Engineer position. This position will provide Quality Assurance oversight and ensure compliance in the support of combination device development life cycles. | 09/22/2025 |
| 490 | REGENXBIO Rockville, MD Clinical Research Associate II Bachelors degree Exp: 1 year |
As a Clinical Research Associate (CRA), you will be responsible for the support and coordination of the logistical aspects of clinical trial management, site management, data review & cleaning according to FDA regulations, Good Clinical Practice (GCP) and relevant SOPs. You’ll act as a pivotal point of contact for the clinical trial team and assist with the coordination of activities associated with the start-up, conduct, and close-out of clinical trials and other duties as assigned. | 09/22/2025 |
| 491 | REGENXBIO Rockville, MD Clinical Research Associate (MPS) Bachelors degree Exp: 1 year |
As a Clinical Research Associate (CRA), you will be responsible for the support and coordination of the logistical aspects of clinical trial management, site management, data review & cleaning according to FDA regulations, Good Clinical Practice (GCP) and relevant SOPs. You’ll act as a pivotal point of contact for the clinical trial team and assist with the coordination of activities associated with the start-up, conduct, and close-out of clinical trials and other duties as assigned. | 09/22/2025 |
| 492 | Renaissance Lakewood, NJ MS&T Scientist II Master's Degree in Pharmaceutical Sciences, Formulation Chemistry, Chemical Engineering, or similar degree Exp: 1-3 years |
Perform MS&T activities with limited supervision for pharmaceutical products, including parenteral and nasal products for all new products from scale-up to commercialization and process improvement beyond commercialization. Continue to grow in understanding the overall generic and new drug development processes, Agency requirements, and CMC strategies. Understand and comply with all the Renaissance safety, environmental and quality practices and procedures as outlines in organization/departmental guidelines and SOPs, as well as applicable federal, state and local regulations. Ensure all department SOPs are in place and followed. Participate with supervision in the progress of project work with follow-ups, meeting timelines and providing appropriate technical info to the support team. Identify, develop and foster good working relationships with cross-functional teams, external customers and support initiatives required to enhance Renaissance's reputation with customers continually. This role may also be a scientific team member for client calls regarding MS&T matters. Prepare project protocols and assess and identify deliverables with limited supervision. Review technical data, documents, and proposals. Provide technical guidance with limited supervision on commercial products after launch and development products through technical communications, memos, and reports. Learn to trend data and look to continually achieve and meet specifications, providing Process Capability Analysis. Ensure batch records are written and accurate in a manner that Operations can follow them and ensure Operations are trained and feel confident in the process for commercial batches. Support any regulatory audits as assigned. Must have the ability to work in a team environment. Must comply with all company policies. Flexibility in schedule is required based on business needs. Other duties, as assigned. | 09/22/2025 |
| 493 | Resonetics Hutchinson, MN Manufacturing Engineer Bachelor’s degree in an engineering field Exp: 1 year |
Our Manufacturing Engineer focuses on introducing and establishing new Manufacturing Processes plus Process Maintenance and Continuous Improvement for existing Manufacturing Processes. Additional areas of focus may include: setup reduction, operator training, tool design or selection, performance metrics, and drafting development plans. Other daily responsibilities will include: procedure generation, participation in production readiness activities for new clients and designing continuous improvement plans for current production jobs. As improvements are identified, it will very likely be the responsibility of this individual to document, implement, train and re-qualify any changes. | 09/22/2025 |
| 494 | Restor3d Durham, NC Supply Chain Analyst Bachelor’s degree Exp: 1+ year |
The Supply Chain Analyst will be responsible for maintaining ERP data and developing analytics meet the Company’s Sales & Operations Plans and Quality Objectives. Ideal candidates will be local to Durham, NC and have experience providing supply chain data analytics and reporting for medical device manufacturers. | 09/22/2025 |
| 495 | Revolution Medicines Redwood City, CA Safety Scientist MSc in a Life sciences discipline Exp: 1+ years |
The Safety Scientist within Global Patient Safety Science is an individual contributor who provides safety science and pharmacovigilance support to all products across the RevMed portfolio, which includes early and late phase development activities. The individual will be responsible for supporting clinical studies, review of clinical trial protocols, supporting updates to IBs, ICFs, and authoring of DSURs. Additional safety related activities will involve medical review of individual case safety reports (ICSRs), safety surveillance of assigned products and active member of cross-functional teams. | 09/22/2025 |
| 496 | Revolution Medicines Redwood City, CA Clinical Trial Assistant BS or BA in relevant scientific discipline Exp: 0-3 years |
This is a unique opportunity for an entry-level Clinical Operations Professional. As a Clinical Trial Assistant (CTA), you will be responsible for providing administrative and operational support for one or more studies within a clinical program. Reporting into the Associate Director, Clinical Operations you will play a critical role in executing well-defined tasks that support clinical study start-up, maintenance, and close-out. | 09/22/2025 |
| 497 | Revolution Medicines Redwood City, CA Temp Senior Research Associate, Assay Technologies, Lead Discovery Master’s degree in biochemistry, biophysics, biotechnology, or related field Exp: 0-3 years |
We are looking for an experienced Senior Research Associate to help the Discovery Sciences team accelerate our search for new oncology therapeutics. The successful candidate will join a high-performing team of experts in the use of biochemical and biophysical screening techniques to drive the efficient identification and rapid development of clinically impactful drugs against frontier targets in oncology. Working from the bench, they will apply their biochemical and biophysical expertise. The candidate will support Discovery Science efforts to enhance how we discover inhibitors of established and new drug target proteins, as well as contribute to our mission of providing high-quality experimental data for existing programs. | 09/22/2025 |
| 498 | RION Rochester, MN Associate, Quality Control B.S. or M.S. Exp: 0-3 years |
Independently develop, validate, and oversee the performance of testing methods designed to characterize cell-based therapeutic products at various stages of product development. Perform release and stability testing on GMP and non-GMP biologic therapeutic products for both human and veterinary programs. | 09/22/2025 |
| 499 | RION Rochester, MN Research Associate, Analytical Development Bachelor's or Master's degree with focus in Biological Sciences Exp: 1+ years |
The Analytical Development Research Associate will contribute to analytical method development, implementation, and pre-qualification of methods focused on Rion’s exosome technology. This role will work closely with Rion Quality Control to execute method transfers and support continuous improvement. As such, the candidate will possess the technical skills required to conduct experiments and assays in a wet lab environment involving techniques such as mammalian cell culture, ELISA, RT-qPCR, HPLC and colorimetric/fluorometric-based assays. The Analytical Development Research Associate will be responsible for the execution of experiments, as well as data interpretation and final reporting. The position affords the opportunity to serve as a key member of Rion’s scientific team and contribute to the advancement of exosome therapeutics. The Analytical Development Research Associate will work closely with the Analytical Development Scientists and support the efforts of Quality Control/Process Development. As such, the successful candidate will work in an upbeat, highly collaborative and dynamic environment. Additional responsibilities associated with this position will involve assisting in day-to-day laboratory operations such as inventory management, procurement, and general laboratory and equipment maintenance. | 09/22/2025 |
| 500 | Rivanna Medical Charlottesville, VA Product Development Engineer Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, or a related engineering discipline Exp: 1-3 years |
RIVANNA is seeking a Product Development Engineer to join our dynamic engineering team. You will work with a talented team of professionals as we strive to achieve our mission to develop and commercialize world-first imaging-based medical technologies that elevate global standards of care. As a Product Development Engineer, you will contribute to activities across the product lifecycle, from prototype development to clinical support. This hands-on multidisciplinary role involves close collaboration with the mechanical, manufacturing, and electrical engineering team on a wide range of product development tasks and projects. This job will be on-site in Charlottesville, VA; applicants must be local or willing to relocate to Charlottesville for this position. | 09/22/2025 |
| 501 | RQM+ Cary, NC Clinical Trial Associate B.S/B.A. degree in science/healthcare related field Exp: 1 year |
The Clinical Trial Associate supports the Clinical Trials team(s) in the overall management and administration of trials, including planning, execution, and closeout of one or more clinical trials in a fast-paced environment. The primary responsibility is to manage administrative tasks on behalf of the team. | 09/22/2025 |
| 502 | Sanofi Framingham, MA Manufacturing Compliance Engineer II Master's degree in sciences, Technical, Engineering Exp: 1 year |
Manufacturing Operations is responsible for supporting large scale mammalian cell culture and multi-stage large scale chromatography manufacturing operations as part of a 24/7 large-scale therapeutic protein or vaccine manufacturing facility. Operation’s main functions are leading deviation investigations and managing CAPA Implementation, partnering with direct manufacturing staff for enhancing and improving the manufacturing instruction set, overseeing and supporting manufacturing’s traini8ng program, and identifying and managing continuous improvement initiatives. Manufacturing Compliance Engineer II uses expert knowledge of compliance and GXP manufacturing processes to manage investigation and improvement initiatives within manufacturing operations. | 09/22/2025 |
| 503 | Sanofi Framingham, MA Senior Manufacturing Technician Bachelor's degree in Biotech Exp: No exp |
This is a 12 hour, rotating position in a large scale cGMP biologics facility. The Sr. Manufacturing Technician will be responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMPs. | 09/22/2025 |
| 504 | Sanofi Pearl River, NY Production Technician USP BS degree Exp: 1-3 years |
Primary responsibility of the incumbent will be operation of general manufacturing equipment under close supervision in accordance with current relevant quality standards or standardized procedures and within safety guidelines in the production of Flublok Drug Substance in the large-scale recombinant protein production operations of the cGMP commercial manufacturing facility. Requires good documentation skills and attention to detail. Duties will include the operation, maintenance, cleaning and sanitization of large-scale cell culture bioreactors and associated operations such as media preparation, infection, and harvest. Activities will include executing techniques such as large-scale bioreactor cell expansion with the use of stainless-steel vessels and single use bioreactors (SUBs) including transfer lines, ancillary equipment (tube welders, tube sealers, peristaltic pumps), use of water-for-injection (WFI) point of use taps, etc. | 09/22/2025 |
| 505 | Sanofi Swiftwater, PA Production Technician - Vaccines Bachelor’s degree in Life Sciences or other relevant field Exp: No exp |
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. | 09/22/2025 |
| 506 | Saptalis Hauppauge, NY Quality Control Scientist BS/MS Degree (chemistry or related field) Exp: 0-2 years |
Saptalis is looking to recruit QC Scientists to join the growing Quality group at our facility in Hauppauge, NY. QC Scientist is responsible for GMP testing of raw materials, in-process, finished product and stability samples for release. In addition, the responsibilities include maintaining laboratory equipment, assisting in investigations and coordinating external testing as needed. | 09/22/2025 |
| 507 | Serán Bend, OR Scientist/Engineer, Drug Product Development Bachelor or Master’s degree in pharmaceutical science, chemistry, chemical engineering, biological engineering, mechanical engineering, materials scie Exp: 1 year |
Serán seeks to hire a Scientist/Engineer to join the Drug Product Development group and contribute as part of an interdisciplinary team to develop and scale-up pharmaceutical manufacturing processes. The role requires strong hands-on laboratory skills and the ability to apply fundamental scientific principles to solve problems. Strengths in data collection, analysis, proactive communication, and continuous learning by textbooks, journals, and training will enable the successful candidate to thrive. The ideal candidate would enjoy a work environment that is both science-focused and adaptable to meet rapidly changing project needs. Preference will be given to candidates with higher experience levels. | 09/22/2025 |
| 508 | Siemens Buffalo Grove, IL Mechanical Engineer - Hardware & Devices Bachelor’s degree in mechanical engineering or another related field Exp: Entry level |
Design and develop mechanical hardware and devices Work with senior engineering personnel, mechanical engineers, lab engineers, technical writer, approvals manager, technicians, and others within the organization to coordinate development of designs. Generate development and product costs, schedule, and mechanical engineering specifications to support design team and adjacent functions. Provide support of existing products, drive Cost Value Engineering efforts, and assist in the development of new mechatronic products. Assemble or direct the assembly of mechanical hardware and systems and other tasks. Use engineering and other software for project management, engineering, development (3D modelling), and report writing. Prepare rough copy of technical documentation to support product designs. Work with outside vendors to optimize design and obtain costing for production quantities and tooling. Assist field employees in trouble shooting product problems in field offices, distributors, or customer locations. May visit suppliers to assist in resolving their production problems. Generates development and product cost, schedule, and mechanical engineering specifications to support design teams. Create models and drawings for components and assemblies using CAD software. Coordinate the design, sourcing, assembly, and testing of concept models to validate production ready designs. Initiate and execute change requests driven by new product introduction, design-to-cost efforts, supplier change etc. | 09/22/2025 |
| 509 | Siemens Wendell, NC Electro-mechanical Quality Test Technician- 2nd Shift Bachelor’s degree in electrical engineering Exp: 1+ years |
We are looking for an Electro-mechanical Quality Test Technician for our Motor Control Center (MCC) team on 2nd shift. This position will be based in Wendell, NC. The Electro-mechanical Quality Test technician is responsible for performing final test and inspection duties on Low and Medium Voltage Electrical Distribution Equipment, such as Switchgears, Switchboards and Breakers. | 09/22/2025 |
| 510 | Siemens Healthineers Newark, DE System Engineer Bachelor’s degree in Mechanical/Electrical/Chemical Engineering or related discipline Exp: 0-3 years |
Learn and apply mechanical and/or electrical process automation principles and technology to design, develop, document, install, qualify, and optimize new and upgrade existing automated medical diagnostic consumable device manufacturing equipment, batch processing systems, and semi-finished reagent formulation systems in a constantly changing fast-paced environment. Work closely with cross-functional senior design team members to develop understanding of subsystem/system functionality and performance. Supporting troubleshooting, determining root cause, and then implementing design modifications as they pertain to highly complex automated production assembly and packaging system performance. Work within small projects teams for business expansion, quality improvements or efficiency improvements to existing equipment. Execute experiments to generate and collate system performance test data to support establishing acceptance criteria. Develop technical writing skills by creating technical documentation such as validation documentation, functional specifications, user requirements, and manufacturing work instructions. Assure compliance to all design characterization, integration and verification quality procedures and policies of process development and validation. Collaborate with Senior level System Engineers, Technical Operations and Manufacturing teams. Providing routine off-hour process support for mechanical equipment issues, typically one week in every 10 to 12 weeks, or as required. | 09/22/2025 |
| 511 | Siemens Healthineers Walpole, MA Laboratory Technician BS/BA in related discipline Exp: 0-2 years |
In your activities you will execute the build of large-scale automated equipment in Walpole Formulation. You will assist in meeting product demand requirements: manufacturing product, allocating bill of materials and routings. You will assist in calibration and maintenance of lab equipment, and lab duties as required. You will work within a regulated laboratory environment: knowledge of and compliance with ISO, GMP, QSR. You will work with laboratory software: knowledge of Microsoft Office, basic understanding of SAP. You will demonstrate a basic knowledge of professional principles and skills. You will use fundamental concepts, practices, and procedures of the particular area of specialization. You will assist in fostering the team environment. Your contacts will be primarily with immediate manager and others in the group. This position includes the handling of all types of materials, including hazardous and DEA (Drug Enforcement Agency) controlled materials. | 09/22/2025 |
| 512 | Siemens Healthineers Newark, DE External Manufacturing Operations Engineer M.S. in Chemistry, Biochemistry, Engineering, Medical Technology, Biology, or a related discipline Exp: 1-3 years |
Serve as the primary liaison with OEM partners for all manufacturing-related activities involving finished products within the Laboratory Systems Business Unit. Ensure adherence to Siemens Healthineers’ Quality Management System. Familiarity with Supplier Corrective Action Reports (SCAR) and Corrective and Preventative Actions (CAPA) is highly desirable. Review and approve verification, qualification, and validation protocols and results conducted at OEM sites, particularly during the commissioning of key equipment and components for Siemens-owned, supplier-operated assets. Lead or coordinate in-house testing when necessary. Provide technical assessments for Supplier Change Notices, including changes to manufacturing processes, raw materials, in-process testing, equipment, and manufacturing locations, in collaboration with Technical Operations. Lead and coordinate escalations of OEM-initiated change notices to the Change Review Board (CRB), including associated documentation and testing. Manage the implementation of Siemens Healthineers-initiated changes at OEM sites. Manage capital and expense budgets for Siemens-owned, supplier-operated equipment. Collaborate with suppliers and Siemens finance teams to ensure assets are properly funded, maintained, and have sufficient capacity. Prepare and submit Applications for Investment (AFIs) as needed. | 09/22/2025 |
| 513 | Siemens Healthineers Palo Alto, CA Product Quality Engineer Master's degree in Engineering Exp: No exp |
Varian, a Siemens Healthineers company is seeking a dedicated and detail-oriented Product Quality Engineer to join our team in Palo Alto, California. In this position, you will play an instrumental role in engaging with our local and global partners, driving various transformation initiatives and providing daily support to our manufacturing operations. | 09/22/2025 |
| 514 | Sino Biological Houston, TX Downstream Associate Bachelor’s degree in Biology, Biochemistry, Biotechnology, or a related field Exp: 0-3 years |
This is an entry-level position suitable for individuals seeking hands-on experience in protein purification and quality control in an industrial bioprocessing environment. The Associate will support the downstream team in executing purification workflows and conducting protein characterization assays to evaluate product quality. Responsibilities include chromatography-based purification, recombinant protein QC related tasks under the guidance of project scientists. This role requires strong attention to detail, good lab documentation practices, and effective collaboration with cross-functional teams. | 09/22/2025 |
| 515 | Singota Solutions Bloomington, IN Associate QA Specialist - Quality Events Bachelor’s Degree in Science related field Exp: 1-3 years |
The Associate QA Specialist - Quality Events position is responsible for supporting and maintaining the GMP-compliant quality systems related to deviations and CAPAs (Corrective Action & Preventative Action). This role provides quality oversight of quality event lifecycle management, ensures adherence to internal procedures and regulatory requirements, and interfaces directly with internal teams, external clients, and regulatory bodies. This position plays a key role in maintaining site compliance and driving continuous improvement across operations. | 09/22/2025 |
| 516 | Revvity Hebron, KY Associate Quality Assurance Engineer Bachelor’s degree Exp: 0-2+ years |
This position supports the review of client records for any HCT/P that is sent for clinical trial participation, transplant, or research and review of batch records for contract processing. This role supports the day-to-day needs of the company regarding change management and controlled documents. This role is also involved in various initiatives within the Quality department, which includes the overall processes of the maintenance and archival of records. Supporting internal quality activities that relate to the overall operation of the site’s quality program. | 09/22/2025 |
| 517 | Revvity San Diego, CA Research Associate II - Cell Analysis Bachelor’s Degree in life sciences or other relevant field Exp: 1+ years |
At BioLegend (a Revvity, Inc. company) we develop novel, cutting edge products and offer custom services to help with scientific innovation and discovery. We are currently looking for a talented, detail oriented person to join our growing Product Development team. The potential candidate will assist with development of new products for cell analysis such as antibodies, multi-color panels, and reagents for analysis of cell metabolism and cell imaging. The successful candidate must be a self-motivated, team player, able to communicate effectively with a multi-disciplinary team and must possess excellent organization skills. | 09/22/2025 |
| 518 | SK Pharmteco Rancho Cordova, CA Quality Chemist I Bachelors degree Chemistry, Microbiology or Related Field Exp: 0-1 years |
The Quality Control Chemist I will be responsible for analyzing and making determinations as to the quality of a product, using analytical equipment pertinent to the appropriate application of skills. This position provides solutions to a variety of technical problems of moderate scope and complexity. Work is closely supervised. | 09/22/2025 |
| 519 | Sofie Totowa, NJ Environmental Monitoring Technician Bachelor’s Degree in a Life Science discipline Exp: 0-3 years |
The Microbiology - Environmental Monitoring Technician supports microbiology and manufacturing activities at the NJ5 site by (1) performing Environmental Monitoring (EM) as per sampling schedules (2) detecting, quantifying, identifying, and aiding in investigations for possible contaminants that may impact the quality of product during different stages of the manufacturing process. | 09/22/2025 |
| 520 | Sovereign Pharmaceuticals Fort Worth, TX QC Lab Technician BS Related scientific field Exp: 1-2 years |
The primary function of a QC Laboratory Technician is to perform the following duties: Sample receipt (logging and labeling) of all samples into the lab, verifying documentation, DEA forms, etc., and entering into Excel to aid laboratory scheduling by supervision. Ordering reagents/standards/office supplies and submitting to purchasing. Glassware cleaning. Solution/standard preparation. DEA reconciliation of completed samples. Receiving reagents/consumables. Inventory management (full inventory of reagents in the lab each week). Receiving and tracking reference standards. General house-keeping such as stocking consumables. Destruction of completed noncontrolled samples. Assist with Stability Program management (sample placement/retrieval from the chambers). Assist with retaining sample storage/retrieval | 09/22/2025 |
| 521 | Sovereign Pharmaceuticals Fort Worth, TX QC Chemist I BA/BS Chem Exp: 0 years |
The primary function of a QC Chemist is to perform qualitative and quantitative chemical and physical analysis in support of raw materials, in-process samples, components, and finished drug products testing. | 09/22/2025 |
| 522 | Sovereign Pharmaceuticals Fort Worth, TX QC Chemist II BA/BS Chemistry Exp: 1 year |
The primary function of a QC Chemist II is to perform to a high level in qualitative and quantitative chemical and physical analysis in support of two of the following areas: Analysis of raw materials and packaging components. Analysis of in-process and finished drug products (including stability) of primarily high-volume products. Analysis of high potency products | 09/22/2025 |
| 523 | Genentech South San Francisco, CA Bioprocess Technician - Clinical Supply Center Bachelor Degree Exp: 1-3 years |
The Clinical Supply Center Bioprocess Technician is an integral member of the Clinical Supply Center (CSC) team in South San Francisco (SSF). The SSF CSC is a state-of-the-art large molecule drug substance facility which supports GMP production for phase 1, 2 and early phase 3 clinical trials. The CSC employs a ballroom design, utilizing single-use technology, new analytical techniques and digital manufacturing systems to deliver a best in class bioprocess facility. We are looking for individuals to support this facility who are comfortable with ambiguity, have an entrepreneurial spirit within a GMP environment, have demonstrated strong Pharma Technical Behaviors, and have an agile mindset. Ability to collaborate is crucial as success will be measured as a member of a team, not just as an individual. Ideal candidates would have experience in a broad range of functional roles in support of biopharmaceutical production. | 09/22/2025 |
| 524 | Penumbra Alameda, CA Manufacturing Engineer I, Operations Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering or related degree Exp: 1+ years |
The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and that support continuous improvement in production. Project opportunities are designed to develop professional work knowledge and abilities and to support the efforts and projects that have global importance to the success of the business. Area of work involves manufacturing and business processes with interaction between production, cross-departmental engineering groups, and other cross-functional teams (such as Regulatory, Quality, R&D, Supply Chain, IT, etc.) in executing and coordinating business operations systems projects and activities. Essential job functions include creating and executing an integrated cross-functional project plan. | 09/15/2025 |
| 525 | Penumbra Alameda, CA Manufacturing Engineer II, Operations Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering or related degree Exp: 1+ years |
The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and that support continuous improvement in production. Project opportunities are designed to develop professional work knowledge and abilities and to support the efforts and projects that have global importance to the success of the business. Area of work involves manufacturing and business processes with interaction between production, cross-departmental engineering groups, and other cross-functional teams (such as Regulatory, Quality, R&D, Supply Chain, IT, etc.) in executing and coordinating business operations systems projects and activities. Essential job functions include creating and executing an integrated cross-functional project plan. | 09/15/2025 |
| 526 | Pfizer Andover, MA Process Engineer II Bachelor's degree Exp: 0+ years |
Execute production activities using knowledge of process equipment, systems, and manufacturing operations. Participate in operational qualification training and assist the Team Lead as needed. Ensure all activities comply with Company policies, standard operating procedures, Pfizer Values, and global regulatory and environmental guidelines. Work in a structured environment using established procedures. Ensure work is regularly reviewed for technical judgment, completeness, and accuracy. Assist in troubleshooting, technology transfer, and start-up activities. Oversee technical documentation for production and process approvals, ensuring compliance with Current Good Manufacturing Practices, and manage process activities by adhering to Standard Operating Procedures. | 09/15/2025 |
| 527 | Pfizer Groton, CT Quality Operations Drug Product: Associate Bachelor's degree Exp: 0+ years |
This Quality Operations (OQ) position will support the Groton, CT PharmSci Small Molecules QO department by assisting in quality operations activities related to the manufacture and disposition of GMP clinical Drug Product. As an Associate Operations Quality colleague, the successful candidate will have quality touchpoints prior to the start of drug product manufacturing through disposition of final drug products for clinical use. Paramount to this role will be acting as a quality point of contact for supporting investigations and ensuring compliance with regulatory and internal standards. | 09/15/2025 |
| 528 | Pfizer Rocky Mount, NC Senior Automation Engineer Master's degree Exp: 0+ years |
As a Sr. Automation Engineer your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate explaining difficult issues and establishing consensus between teams. | 09/15/2025 |
| 529 | Pfizer Rocky Mount, NC Automation Engineer Bachelor's degree Exp: 0+ years |
As an Automation Engineer your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate in explaining difficult issues and establishing consensus between teams. | 09/15/2025 |
| 530 | Pfizer Groton, CT In Vivo Technician Specialist, Drug Safety R&D Bachelor of Science degree, Biological Sciences (or equivalent) Exp: 0-2 years |
The In Vivo Technician role functions within study execution and provides non-Good Laboratory Practice (GLP) and GLP in vivo study conduct expertise to advance the Pfizer portfolio, particularly for the selection of new therapeutic candidates but also for support of later stages of clinical development and registration. The In Vivo Technician is responsible for performing accurate, high quality in-life study work for rodent and non-rodent safety studies in compliance with the study protocol, Standard Operating Procedures (SOPs), Good Laboratory Practice (GLP) regulations, Environmental Health and Safety (EHS) standards, animal welfare regulations, and departmental policies/procedures. The data collected on these studies by the In Vivo Technicia | 09/15/2025 |
| 531 | Pharmaron Exton, PA Associate Scientist, In Vivo PK Bachelor of Science (Biology, Biochemistry, Pharmaceutical Life Sciences) Exp: 1 year |
The Associate Scientist will play an integral role in growing the operations and customer base by supporting the analysis of various samples and performing studies/assays independently while delivering exceptional quality with a high attention-to-detail and ensuring client expectations are met. | 09/15/2025 |
| 532 | Pharmaron Exton, PA GMP QC Analyst I Bachelor's or Master's degree Exp: 0-3 years |
We are seeking a highly motivated GMP QC Analyst I/ II to join our Cell & Gene Therapy (CGT) Quality Control team. The QC Analyst I/ II will be responsible for executing routine laboratory testing under cGMP conditions to support multiple client projects in various phases of development. This role is suitable for candidates seeking to gain hands-on experience in a dynamic, client-focused, cross-functional CGT laboratory. The ideal candidate will have a strong foundation in biological sciences and laboratory techniques, along with a commitment to quality and regulatory compliance. | 09/15/2025 |
| 533 | Pharmaron Exton, PA GMP QC Analyst II Master's degree Exp: 1-3 years |
We are seeking a highly motivated GMP QC Analyst I/ II to join our Cell & Gene Therapy (CGT) Quality Control team. The QC Analyst I/ II will be responsible for executing routine laboratory testing under cGMP conditions to support multiple client projects in various phases of development. This role is suitable for candidates seeking to gain hands-on experience in a dynamic, client-focused, cross-functional CGT laboratory. The ideal candidate will have a strong foundation in biological sciences and laboratory techniques, along with a commitment to quality and regulatory compliance. | 09/15/2025 |
| 534 | Pharmaron Exton, PA Quality Control Associate Bachelor's degree in pharmaceutical sciences, life sciences or a related scientific field Exp: 1+ years |
The Quality Control Associate will be responsible for review and drafting of data and reports generated in support of DMPK and CGT studies at Pharmaron US lab Services. | 09/15/2025 |
| 535 | Quest Diagnostics Cleveland, OH Bio-Analytical Instrument Technician BA/ BS degree or above (preferably in science, engineering, or computer information) Exp: 1-2 years |
Provides assistance to internal clients and is accountable for working independently with minimal supervision. The position requires strong communication skills both verbal and written plus technical skills to accomplish job responsibilities. | 09/15/2025 |
| 536 | Quest Diagnostics Lenexa, KS Forensic Toxicology Laboratory Scientist I Bachelor’s Degreee Exp: 1 year |
This position works within the Forensic Toxicology Laboratory and is responsible for all aspects of testing of donor specimens including specimen preparation and instrument operation. | 09/15/2025 |
| 537 | Quest Diagnostics San Juan Capistrano, CA Bio-Analytical Instrument Technician BA/ BS degree or above (preferably in science, engineering, or computer information) Exp: 1-2 years |
Provides assistance to internal clients and is accountable for working independently with minimal supervision. The position requires strong communication skills both verbal and written plus technical skills to accomplish job responsibilities. | 09/15/2025 |
| 538 | Quest Diagnostics Shelton, CT Cytogenetics Technician I Bachelor of Science (Biology or Chemistry Preferred) Exp: 1 year |
Perform various routine laboratory functions in a precise and accurate fashion to assist the laboratory professional staff and to facilitate production. | 09/15/2025 |
| 539 | Quest Diagnostics Greensburg, IN Medical Laboratory Scientist I Generalist BS/BA in Chemistry or Biology Exp: 1 year |
Are you intrigued by the science of the human body? Curious about state-of-the-art laboratory instrumentation? Looking to join a Fortune 500 company leading the world in providing diagnostic information services? Quest Diagnostics is now recruiting for technologist positions ranging from entry level to experienced, with a wide range of benefits and training! | 09/15/2025 |
| 540 | Quest Diagnostics Kokomo, IN Medical Laboratory Scientist I Generalist BS/BA in Chemistry or Biology Exp: 1 year |
Are you intrigued by the science of the human body? Curious about state-of-the-art laboratory instrumentation? Looking to join a Fortune 500 company leading the world in providing diagnostic information services? Quest Diagnostics is now recruiting for technologist positions ranging from entry level to experienced, with a wide range of benefits and training! | 09/15/2025 |
| 541 | Phlow Richmond, VA Scientist, Engineering BS or MS in Chemical engineering Exp: 0-5 years |
The purpose of this role is to provide engineering support to Phlow’s Manufacturing Science and Technology (MS&T) group. This is an exciting opportunity for recent graduates or individuals with process engineering experience to independently design, install, and operate continuous and batch processing equipment under the direction of a Principal Scientist or other team member. The candidate will provide engineering support to the MS&T group including equipment selection and design, heat and mass transfer calculations, and scale-up modelling. The candidate will support execution Phlow’s internal API development projects as well as the CDMO business to ensure business objectives are met. The candidate will ensure excellence of our process development and technical transfer to Phlow’s partners or customers. The candidate will personify Phlow’s shared values and culture, both internally and externally. The candidate will work with the highest standards of safety, integrity, transparency, and ethics to create win-win scenarios for patients, customers, partners, and colleagues. | 09/15/2025 |
| 542 | Phlow Richmond, VA Laboratory Assistant B.S degree in Chemistry, or related scientific field Exp: 1+ years |
This role contributes to Phlow's mission by supporting laboratory work related to analytical chemistry and process development. The position involves performing laboratory operations activities in Phlow’s R&D laboratories located in Richmond and Petersburg, under the guidance of the Senior Director, Analytical Chemistry, or other team members. This position is a full-time, day shift position, Monday-Friday. The expected schedule will involve rotating days during the week between the Petersburg and Richmond locations. The team member plays a critical role in ensuring Phlow’s ability to conduct contract development and manufacturing services and the successful execution of both internal API development projects and commercial initiatives. Responsibilities include safety and housekeeping, inventory and procurement of supplies, equipment maintenance or calibration, collaborating with scientists to meet business objectives and timelines, and upholding Phlow’s shared values and culture in all interactions, both internally and externally. This role requires maintaining the highest standards of safety, integrity, transparency, and ethics in all aspects of work. By doing so, the team member contributes to delivering outcomes that create win-win scenarios for patients, customers, partners, and colleagues while fostering an innovative and collaborative environment at Phlow. | 09/15/2025 |
| 543 | Pledge Therapeutics Canton, MA Research Associate, Immuno-Oncology MS Exp: 1-2 years |
We seek an enthusiastic and curious scientist interested in participating in all aspects of the hit-to-lead drug discovery process. The opening is at our new state-of-the-art facility in Canton, MA. The successful candidate will engage in the Immuno Oncology research areas of the company and will work with a successful team of international senior scientists located in the USA and EU. The ideal candidate will have great communication skills, excellent technical skills, exemplary attention to detail, and a passion for learning. This position will have the opportunity to make significant scientific contributions to numerous drug discovery projects. | 09/15/2025 |
| 544 | Pledge Therapeutics Canton, MA Research Associate, Virology Bachelor’s or Master’s degree in biological sciences or a related field Exp: 0-2 years |
We seek an enthusiastic and curious scientist interested in participating in all aspects of the hit-to-lead drug discovery process. The opening is at our state-of-the-art facility in Canton, MA. The successful candidate will engage in the company’s virology research areas and work with a successful team of scientists in the USA and EU. The ideal candidate will have great communication skills, excellent technical skills, exemplary attention to detail, and a passion for learning. This position will have the opportunity to make significant scientific contributions to numerous drug discovery projects. | 09/15/2025 |
| 545 | PolyPeptide San Diego, CA QC Chemist BS degree in Chemistry or Biochemistry or equivalent Exp: 1+ years |
The Quality Control Chemist performs analytical testing on raw materials, intermediates, and finished peptide products using a range of laboratory instruments to ensure compliance with quality standards and GMP guidelines. This role prepares samples, calibrates equipment, documents results, and identifies potential quality issues, supporting the development of corrective actions as needed. The chemist also contributes to SOP development and maintains a clean, compliant laboratory environment. This role contributes directly to PolyPeptide’s commitment to delivering exceptional quality and on-time delivery to our customers. | 09/15/2025 |
| 546 | Precigen Germantown, MD GMP Gene Therapy Manufacturing Associate Bachelor’s degree or Master’s degree in biology, biomedical science, or life science Exp: 1-3 years |
We are seeking a hard-working GMP Gene Manufacturing Associate I/II (level determined by candidate experience) at our Germantown, MD location to join us in our mission to serve patients with our next generation of innovative Gene Therapies. This position will require a professional who thrives in a dynamic team environment, brings meticulous attention to detail in the quality of their work and is proactive in implementing improvements. This position will perform a broad range of tasks in the cGMP manufacturing of clinical and commercial adenovector products. Prior experience in GMP manufacturing and operation of GMP process equipment are required. | 09/15/2025 |
| 547 | Proclinical Wilmington, DE Staff Scientist, ADME Bachelor's degree in biology, Life Science, or related discipline. Exp: 0-3 years |
Proclinical is working alongside a pharamceutical company seeking a Staff Scientist to join the team. The Staff Scientist, DMB is primarily responsible for DMPK support of discovery and/or development projects regarding in vivo pharmacokinetics studies. The successful candidate will involve preparing doses for, scheduling, and coordinating in vivo pharmacokinetics studies as well as generic lab functions with the opportunity for cross training on in vitro assay support. | 09/15/2025 |
| 548 | Proclinical Wilmington, DE Chemical Library Inventory Specialist BS (or equivalent laboratory experience) in Chemistry/Life Sciences or related field Exp: 0-5 years |
We are seeking a motivated and scientifically curious chemical library specialist to join our client's Discovery Chemistry department and contribute to the development of internal high-throughput screening chemical library. This role offers an exciting opportunity to apply chemistry knowledge towards the discovery of new therapeutic entity. | 09/15/2025 |
| 549 | ProMed Plymouth, MN Manufacturing Engineer 2-Metrology Focus Bachelor's degree in mechanical, quality, or manufacturing engineering Exp: 1 year |
We're seeking a Manufacturing Engineer II with Metrology Focus to join our Manufacturing Operations team. This is an important role that safeguards product integrity and regulatory compliance through advanced metrology systems and precision measurement protocols that directly impact patient safety and market access. We are seeking a Manufacturing Engineer II with Metrology Focus to join our Operations Engineering team at ProMed Molded Products. You'll design and implement metrology systems that ensure dimensional accuracy across manufacturing processes while developing quality assurance procedures that detect non-conformances before product release. Your expertise will establish measurement uncertainty analysis and gauge repeatability studies, validating system capability for reliable quality data. You'll create process validation protocols and documentation systems supporting regulatory submissions, while designing manufacturing work instructions that ensure consistent execution and reduce operator variability in our medical device manufacturing environment. We're only considering candidates from The Minneapolis Metro area. No relocation assistance is available for this role. | 09/15/2025 |
| 550 | PSC York, PA QC Analyst I Bachelor’s degree in related science discipline, i.e. Chemistry, Microbiology Exp: 1-3 years |
We are hiring an entry-junior level QC Analyst I. The QC Analyst I will be responsible for conducting quality control testing in the and ensuring the safety, efficacy, and consistency of products. This role involves rigorous analysis at every stage to ensure compliance with regulatory standards and internal quality guidelines. | 09/15/2025 |
| 551 | PSC San Francisco, CA Commissioning Engineer Bachelor’s degree in engineering or a related technical discipline Exp: 1-3+ years |
We are hiring an experienced Commissioning Engineer to provide comprehensive Commissioning Services for Facilities Capital Projects. In this role, you will be responsible for ensuring the successful commissioning of systems and equipment, from design through to post-handover. You will oversee and coordinate all commissioning activities to ensure systems are properly tested, validated, and ready for operational use, in line with project specifications and industry standards. | 09/15/2025 |
| 552 | Psomagen Rockville, MD Junior Bioinformatics Scientist Bachelor’s or Master’s degree in Biology, Bioinformatics, Computer science, or similar degree Exp: 1-3 years |
Do you want to apply your talent and expertise in making a difference by helping scientists answer important questions related to human health and treating diseases? If so, Psomagen is the right place for you. We are a leading company in the genomics field, based in the U.S., seeking a skilled and motivated Bioinformatician to join our Department of Bioinformatics. This role involves managing operation systems, NGS data QC and analysis, and collaboration with the teams. | 09/15/2025 |
| 553 | Psomagen Rockville, MD NGS Laboratory Technician/Scientist/Manager Bachelor’s degree in biology or relevant major Exp: 1 year |
Psomagen Inc. is a leading multi-omics service provider specialized in NGS, Sanger, single cell sequencing services to support life science research and industry field in North America. The NGS clinical laboratory technologist will perform day-to-day NGS experiments including sample preparation, library preparation, QC procedure as well as various NGS instrument operations. | 09/15/2025 |
| 554 | Purdue Pharma Wilson, NC Quality Specialist I, Chemist BA or BS degree in Chemistry or closely related science Exp: 6 months - 2 years |
The Quality Specialist I, Chemist is responsible for supporting the operations and manufacturing process by performing routine and non-routine analytical testing and GMP review in support of the analysis of raw materials, packaging components, ancillary solutions, in-process samples, finished product method development and/or transfers, cleaning/process validations, and stability samples. Will follow standard procedures in accordance with cGMP, GLP, DEA and company policies and procedures. | 09/15/2025 |
| 555 | QIAGEN Germantown, MD Senior Technical Associate Bachelors degree Exp: 0-2 years |
The Senior Technical Associate, Production Molecular Biology must comprehend and perform scheduled routine bulk formulation production tasks according to established procedures in compliance with applicable regulations, including troubleshooting with assistance. | 09/15/2025 |
| 556 | QIAGEN Frederick, MD Contract Quality Assurance Associate Bachelor of Science degree in biology, chemistry, or related field Exp: 1-2 years |
The Contract Quality Assurance Associate supports operations with the implementation and maintenance of new products, procedure development, and validation. This position conducts inspection/release of manufactured product. S/he is a self-starter with strong work ethics, organizational skills, communication skills, critical thinking, attention to detail and accuracy, as well as the ability to work independently and in a team environment is essential. | 09/15/2025 |
| 557 | Quality Agents Various Locations, MA Quality Assurance Specialist BS in a technical discipline (Engineering, chemistry, microbiology, biology) Exp: 0-2 years |
Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. Our Quality Assurance Specialists are leading service providers to our clients providing GMP support. The individual will coordinate validation activities with the client and meet timelines. | 09/15/2025 |
| 558 | QuidelOrtho San Diego, CA Development Associate 1 BS/BA or equivalent in Life Sciences or Chemistry Exp: 1-3 years |
At QuidelOrtho, we are seeking a Development Associate 1 to participate in activities to support research and new product development. The position performs simple experiments as directed by Scientist or Manager. This position will be onsite at our Summers Ridge location in San Diego, CA. | 09/15/2025 |
| 559 | QuidelOrtho Athens, OH Clinical Trials Associate BS/BA in any biological science or Medical Technologist degree Exp: 1-2 years |
As we continue to thrive together QuidelOrtho is seeking a Clinical Trials Associate to support in all clinical team activities for start-up, oversight, and study closure to include coordinating the preparation and assembly of clinical trial supplies and materials for distribution to clinical sites with minimal/moderate supervision. Maintain related tracking information of all clinical materials, shipments, and inventory. Assist the Data Management team in tracking and management of Case Report Forms (CRFs) and Laboratory submission Forms (LSFs). Assist in maintaining files and tracking of all written and electronic documentation for all study records and site interactions in the Trial Master File (TMF). Communicate with sites regarding query resolution to ensure compliance with specified protocols and accuracy of submitted data. Participate in data entry, data auditing, clinical site queries and overall clinical data flow from multiple clinical sites in a timely and professional manner. Coordinate in-house specimen procurement studies. Willingness and ability to learn, understand and apply regulatory guidelines and Good Clinical Practices (GCP’s) applicable to IVD and Medical Devices for conducting clinical field trials, CLIA Waiver and 510(k) submission studies. Be familiar with GCP, FDA regulations and relevant Standard Operating Procedures for clinical research. Develop skill and knowledge with regulatory procedures and become familiar with Quidel product development procedures. Interact with study coordinators and in-house study participants. | 09/15/2025 |
| 560 | QuidelOrtho Rochester, NY Manufacturing Shift Engineer I BS in Engineering (BSME, BSEE or BET is preferred) Exp: 0-2 years |
As the company continues to grow, as one QuidelOrtho we are seeking a Manufacturing Shift Engineer I to work in our Assay manufacturing facility. The Manufacturing Shift Engineer I is an integral member of the Assay Manufacturing Engineering team. This position will support a 24x7 high speed automated manufacturing operation and the associated engineering and maintenance functions when required to troubleshoot high level issues when impacting production. The ability to thrive in a cross-functional collaborative environment is a must. Additionally, the Manufacturing Shift Engineer shall focus on process and equipment improvements with a goal to increase overall equipment effectiveness (OEE). This position is in Rochester, NY. This individual will be working 12 hour shifts and will rotate between day and night shifts. Shift schedule is eligible for shift differential pay. | 09/15/2025 |
| 561 | QuidelOrtho Rochester, NY Engineer II BSc in Engineering or related scientific discipline. Biomedical, Chemical, Mechanical, or Systems Engineering Exp: 1-3 years |
As we continue to grow, we are seeking an Engineer II to join our R&D Field Triage group. This individual will assist in conducting technically challenging investigations to address on-market product quality issues and recommend solutions. This role involves working in a highly collaborative team setting to provide R&D investigational support including design, execution and documentation of experiments to systematically identify failure mode/s and establish root cause/s with clinical laboratory and transfusion medicine products. This position is on-site at our Rochester, NY facility. | 09/15/2025 |
| 562 | Quotient Sciences Philadelphia, PA Staff Formulator Master’s degree in Pharmaceutical Science, Chemical Engineering, or a related field Exp: 1-2 years |
Are you passionate about pharmaceutical science and ready to make a real impact in a fast-paced, collaborative environment? We’re looking for a talented and driven individual to join our team and help bring cutting-edge oral solid dosage forms to life for clinical trials across Phases I–III. | 09/15/2025 |
| 563 | Quva Bloomsbury, NJ QC Laboratory Technician Bachelor’s Degree in life science or related field Exp: 1-2 years |
Our QC Laboratory Technician plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include performing basic laboratory support functions related to the management of laboratory samples, materials, and testing supplies. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. | 09/15/2025 |
| 564 | BioPharmGuy Anywhere, US Contract Data Work some college Exp: 0 yrs |
We are looking for someone with expertise in classifying diseases/conditions by medical specialty to do drug pipeline confirmation tasks. Contract work on a task basis. Must be able to accept payment by PayPal or Venmo. Also must be able to function in the world without using ChatGPT, because if we thought AI could do the task well, you would not be reading this job posting. Please send a message through the contact form if interested. | 09/07/2025 |
| 565 | Lilly Indianapolis, IN Automation Engineer, Drug Substance - Design & Delivery Bachelor of Science Degree in engineering or a related science field Exp: 1 year |
The Engineer – Automation - Drug Substance Design / Delivery role requires a 4-year engineering degree, preferably in Chemical, Mechanical, Electrical Engineering, or related science field. The position requires high learning agility and a background in DCS programming (preferably DeltaV) and experience in automated API manufacturing or related processes. This role will initially be in support of the design and delivery phase of the project, as part of the Global Process Automation & Control Engineering (GPACE) team. As the site nears completion and start-up activities begin, this role will transition into a Lebanon Site role for long term operational support. GPACE is part of Lilly’s Corporate Engineering Tech Center (ETC). GPACE provides automation, measurement, and process control solutions, and is a technical resource for training, standards, capital project delivery, and Lilly’s standard automation platforms. GPACE’s primary customers are global manufacturing and development sites, Manufacturing Information Technology, and peer groups such as Global Facilities Delivery (GFD). | 09/08/2025 |
| 566 | Lilly Indianapolis, IN Engineer – Automation/Process - Serialization Bachelor’s degree in Engineering Exp: 1+ years |
The Engineer - Automation/Process Serialization is accountable for the direct support throughout the design, build, site integration and verification for the new Packaging lines delivered in all Lilly Sites following GSP (Global Serialization Program) processes and procedures. Your role will involve collaborating closely with the Engineering and IT teams (Global and site). | 09/08/2025 |
| 567 | Lilly Indianapolis, IN Environmental Scientist BS or MS Degree in Environmental Sciences, Biology, Chemistry or a relevant field Exp: 0-1+ years |
The Environmental Risk Assessment Group is responsible for preparing environmental risk assessments (ERAs) to support regulatory submissions and environmental stewardship goals. The ERA group outsources studies to determine the physical chemical properties, environmental toxicity, and environmental fate of Lilly active ingredients and related chemicals. Members of the ERA group support issues related to pharmaceuticals in the environment (PiE) and advance the science of environmental risk assessment (ERA). The ERA group is part of the Health Safety and Environment (HSE) function of Lilly Research Laboratories. The ERA group is seeking an enthusiastic, well-organized and detail-oriented individual to manage study contracting, projects, scientific data and documents. The individual will need a science degree in order to understand, review and extract data from technical documents. The individual should enjoy using innovative methods to analyze and improve processes. | 09/08/2025 |
| 568 | Novartis Morris Plains, NJ Cell Processing Specialist I Bachelor’s degree in relevant Engineering or Scientific discipline Exp: 1 year |
The Cell Processing Specialist is responsible for cell washing operations and verifying cell processing intermediate processing days of patient derived clinical and commercial cellular immunotherapy products. The CPS I will also be responsible for the formulation and verification of all media lots. Due to the nature of the starting material (patient cells) this role requires high level of proficiency and ownership of the process and media formulation. | 09/08/2025 |
| 569 | Novartis Cambridge, MA Research Scientist II, Biologics Engineering and Bioconjugation Bachelors or Masters degree in biochemistry, molecular biology or related Exp: 1 year |
We are seeking a highly motivated and creative scientist to join the Biologics Engineering and Bioconjugation (BEC) unit within BRC at Cambridge site. The BEC unit drives a diverse portfolio of biologics drug discovery programs that cover various biologics modalities, such as multi-specific antibodies, non-antibody proteins, ADC and AOC therapies through knowledge-based and structure-based rational design. In this role, you will have the opportunity to learn new and cutting-edge technologies and grow your career in Novartis and in the pharmaceutical industry. This role will help to advance our diverse programs in BRC biologics pipeline and accelerate the discovery process. This associate will mainly work in the lab to support all projects cross the portfolio in the protein engineering function by contributing to protein expression, purification, characterization, and constructs design. | 09/08/2025 |
| 570 | Novartis Indianapolis, IN Maintenance Technician Bachelor's Degree Exp: 1+ years |
The Maintenance Technician is responsible for performing corrective and preventative maintenance and support services for the building(s) and all equipment for a GMP Radioligand Therapies Production Facility. Responsible for reliable, efficient, and sustained operation of the facility and all equipment. Additionally supports current project operations and site goal objectives and ensures compliance with regulatory, corporate, and site requirements related to their functional area. | 09/08/2025 |
| 571 | Novartis Morris Plains, NJ Manufacturing Operations Specialist Bachelor’s degree in a relevant scientific discipline Exp: 1 year |
This role is responsible for working with the Manufacturing Operations team to complete all daily responsibilities for manufacturing support as well as aiding the oversight of all activities occurring in the manufacturing (Shopfloor) area on the 3rd shift to ensure quality and compliance, high performance and scheduled delivery. | 09/08/2025 |
| 572 | Novartis Indianapolis, IN HSE Technician, Isotopes Manufacturing Bachelor’s degree in industrial hygiene, health and safety, engineering, or related field Exp: 0-2 years |
The HSE Technician will be responsible for supporting all HSE compliance aspects at our new state-of-the-art Isotope Manufacturing site. You will help ensure Health, Safety and Environmental activities are managed according to applicable laws and Novartis HSE Management System requirements and assist in the continuous improvement of applicable HSE Management Systems while helping to spread our safety and environmental culture by proactively engaging associates and enhancing awareness. | 09/08/2025 |
| 573 | Novartis East Hanover, NJ Clinical Lab Techician - Scien. Support BA in cell biology, immunology, molecular biology, virology, biochemistry, microbiology, or other related science Exp: 0-5 years |
Under general direction, perform supporting and administrative activities supporting the Raw Materials, BioAnalytics and Microbiology in the Analytical Operations department of TRD CGT East Hanover. | 09/08/2025 |
| 574 | MP Biomedicals Solon, OH Life Science Lab Technician Bachelor of Science in Biochemistry/Chemistry/Biology Exp: 0-3 years |
The Life Science Lab Technician (Technical Manufacturing) performs a wide variety of routine production tasks in Technical Manufacturing and must be capable of producing large-scale components for MP Bio life science products. The Lab Technician must be capable of following work instructions and finish assigned tasks on time. The ideal candidate will have a strong background in Chemistry, Biochemistry, and Biology, attention to detail, time management skills, and the ability to work effectively in a team environment. | 09/08/2025 |
| 575 | NAMSA Atlanta, GA Microbiology Technologist Bachelor degree Exp: No exp |
May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. Accurately collects and records raw data in logbooks and on worksheets. May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. May be required to perform required specific testing as applicable. May be required to operate specified laboratory equipment. May perform Environmental Monitoring, clean and disinfect cleanroom suites (required as applicable). Other duties as assigned | 09/08/2025 |
| 576 | NAMSA Minneapolis, MN Lab Technologist - In Vitro Bachelor’s degree in biology or related scientific field Exp: 1 year |
Executes routine testing per NAMSA SOPs, with appropriate data analysis (cytotoxicity and hemocompatibility). Strictly adheres to GLP guidelines (good documentation, labeling and expiration of materials, participation in audits). Performs maintenance of cell lines through propagation, cell concentration and viability determination, and creation of plates used for standard testing. Performs the extraction process on prepared samples in accordance to ISO, USP and/or JMHLW regulations as directed by study protocol for biocompatibility assays. Communicates with external clients in regards to particulate observations or article abnormality. Routinely communicates with Study Directors and Quality Assurance about issues, results, or audits. Operates, cleans and maintains incubators, autoclaves, hoods, and other equipment routinely utilized. Performs preparation of media/reagents, maintains reagents and/or test article as required for testing, and maintains lab supplies/inventory. Performs data entry, routine calculations, analysis and interpretation of results, and routes all positive results or unusual testing occurrences to Management and/or the Study Director. Responsible for review of incoming test articles and paperwork for appropriateness and accuracy and taking all concerns to management or Study Directors as required. May assist Associates with performing routine test article/product preparation according to work instructions. May communicate test schedule updates to NAMSA Associates or management as needed. Maintains ancillary records (logbooks, worksheets). May be required to perform personal gowning, environmental testing, and submitting organisms from gowning, environmental and sterility test positives for identification and inclusion in monthly trending data, as required for specific testing. Adheres to established company processes. May provide administrative support. May prepare and maintain sterile glassware for the In-vitro lab and sample preparation process. Processes glassware through washer, autoclave and depyrogenation oven as needed. Completes chain of custody documentation for test article tracking. Responsible for daily monitoring of laboratory equipment, being on-call and responding to continuous monitoring alarms. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. May assist in ordering and/or stocking supplies subject to approval. May assist trainers or may become a certified tra | 09/08/2025 |
| 577 | Natera San Carlos, CA Clinical Lab Associate I BS/BA in a biological science or similar field of study Exp: 0-2 years |
Natera is currently seeking a Clinical Laboratory Associate to analyze laboratory specimens following the standard methods and procedures while maintaining equipment and instruments in good operating condition by troubleshooting malfunctions as needed. Schedule is Mon-Fri, from 830am-5pm. | 09/08/2025 |
| 578 | Natera Austin, TX Clinical Lab Operator I BS/BA in a biological science or a related field Exp: 0-2 years |
Assists in analyzing specimens and maintains equipment in good operating condition. | 09/08/2025 |
| 579 | Natera Austin, TX Process Associate 1 Bachelors in Molecular Biology, Biochemistry, Molecular Genetics, or equivalent Exp: 0-2 years |
The Process Associate I (PA-I) within the Process Development - Reagents team (PDO-RGT) works under the guidance of the Reagents QC Development Manager and collaboratively with Scientists within the team to modify existing methods and/or develop and optimize new QC methods to support routine lot release of reagents and kits used in the CLIA laboratory for molecular and genetic based tests. The Process Associate works hands on at the bench to carry out experiments and studies to support bio-chemical verification and validation efforts. The PA-I also supports investigation efforts required for resolving reagent preparation and qualification issues that arise for the CLIA lab. The PA-I works hands-on to carry out experiments and studies with moderate guidance to support process improvement and technical transfer efforts. | 09/08/2025 |
| 580 | NeoGenomics Aliso Viejo, CA Laboratory Technician I - Flow Cytometry, Overnights BS or BA degree is required (in a life or physical science field is strongly preferred) Exp: 1+ years |
Under the direct supervision of licensed personnel, or within a training environment, the Laboratory Technician will assist with responsibilities associated with processing specimens for clinical testing and will provide general support for the laboratory following established policies and procedures. This is the entry level for the Laboratory Technician job category. The employee works in a learning capacity while performing a range of laboratory technician assignments under close supervision. | 09/08/2025 |
| 581 | Neuralink Austin, TX Surgery Mechanical Engineer Bachelor's or Master's Degree in Mechanical Engineering or equivalent Exp: 1-10 years |
The Surgery Engineering team is responsible for developing and managing custom hardware and processes for neurosurgical procedures, excluding the R1 Robot and Operator Station. Their responsibilities encompass the entire surgical process, including patient positioning, incision, craniectomy, precise implant placement, robotic thread insertion success, surgical site irrigation, implant installation, and closure. Additionally, the team ensures safe explantation and upgrade procedures for implants. They also provide mechanical engineering support to the animal care, histology, and BCI teams, contributing to the success of complex neurosurgical procedures and related research activities. | 09/08/2025 |
| 582 | Neuralink Austin, TX Quality Assurance Specialist Bachelor of Science degree, preferably in a science, engineering, or quality-related discipline Exp: 1 year |
The Quality Assurance (QA) Specialist will work with Neuralink's teams to ensure that the appropriate governing body regulations are followed. This includes, but is not limited to, adherence to ISO standards, Good Laboratory Practices (GLP), clinical guidelines, manufacturing protocols, and quality control practices. | 09/08/2025 |
| 583 | Neurona Therapeutics South San Francisco, CA Preclinical Research Associate Bachelor’s degree Exp: 1-2 years |
Our ideal candidates are self-motivated individuals who have clearly demonstrated a passion for scientific research. This is a fantastic opportunity to join a small team, work on transformative science, and build an exciting, science-driven company. Neurona is proud to be an equal opportunity employer and will consider all qualified applicants for employment. | 09/08/2025 |
| 584 | Noah Medical San Jose, CA Manufacturing System Technician BS in Computer Science, Electrical Engineering, or Industrial Engineering Exp: 1 year |
We are seeking a skilled Test Technician to join our team. The ideal candidate will be responsible for testing and troubleshooting medical robotic systems while adhering to Good Manufacturing Practices (GMP). The successful candidate will have a strong understanding of robotic hardware, sensors, motors, PLC’s, relays, circuit boards, computers, cabling and experience with and testing, excellent troubleshooting skills, and GMP experience. | 09/08/2025 |
| 585 | Aptar Pharma Congers, NY Quality Engineer Bachelor’s Degree Exp: 1-5 years |
The Quality Engineer (QE) is primarily responsible for the design and execution of qualification & validation activities, leading the implementation of new or modification of existing manufacturing equipment/processes (e.g. Injection Molding, Assembly), analytical testing equipment and/or facility related systems (e.g. Cleanroom, process gases), in accordance with defined requirements, and customer expectations at the Congers, NY facility. The QE will bring a high-level quality mindset to validations and design transfer, ensuring these activities are thoroughly executed and properly documented in compliance with ISO 15378. The employee will also be involved in leading or supporting continuous improvement initiatives. | 09/08/2025 |
| 586 | Nortech Milaca, MN Manufacturing Engineer Bachelors in Engineering Exp: 1 year |
Apply product design, materials and parts, fabrication process, tooling and production equipment, capabilities, assembly methods, and quality control standards knowledge to develop, evaluate, and improve Nortech’s product design, materials and parts, fabrication processes, fixtures, tooling and production equipment capabilities, assembly methods, and quality control standards. Interact with operations, manufacturing, finance and other internal subject matter experts to define, design, test, implement, and support high-quality, efficient, and cost-effective product tooling and manufacturing processes. Apply Lean, Six Sigma, and FOCUS methodologies to assist with analyzing and planning workforce utilization, space requirements, workflow, and designing equipment layout and workspace for maximum quality and efficiency. Coordinate with Quality and work to establish process controls on new products. Review and estimate production times, staffing requirements, and related costs to inform management decisions. Communicate manufacturing capabilities, production schedules, or other information to facilitate production processes. Participate in vendor discussions, evaluate and recommend equipment product specifications and arrange equipment, material purchase, and parts in partnership with internal subject matter experts. | 09/08/2025 |
| 587 | NorthStar Medical Radioisotopes Beloit, WI Radiopharmaceutical Manufacturing Associate (3rd Shift) Bachelor’s Degree (BS) in a STEM discipline Exp: 1 year |
The Radiopharmaceutical Manufacturing Associate performs duties to support the development and manufacturing of radiopharmaceuticals for NorthStar operations. This includes equipment preparation, product dissolution, and dispensing of medical radioisotopes while complying with procedures, instructions, and prescribed routines. All duties and responsibilities will be completed in compliance with applicable regulatory agency standards. | 09/08/2025 |
| 588 | Nordisk West Lebanon, NH Manufacturing Technician (Multiple Shifts) Bachelors’ Degree in a science discipline Exp: 0 years |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. This is a cleanroom/sterile environment that will require regular gowning, and strict to all procedures in order to ensure the safety of our products for our patients. Prior experience in cleanroom, laboratory, or other sterile environments is a plus, and prior GMP experience is a plus as well. | 09/08/2025 |
| 589 | Novonesis Franklinton, NC Process Engineer I B.S. or M.S. in Mechanical Engineering, Chemical Engineering or Relevant Field Exp: 1-3 years |
We are looking for a dedicated person to provide technical leadership within Supply Chain to ensure products are delivered according to plans within a predictable time frame, volume and quality. You’ll work closely with several departments on site including Quality, Value-Stream (Scheduling), and Operations. You will need an in-depth understanding of our equipment and processes which will be acquired by hands-on experience. On a daily basis you will interact with Operators and Staff members as needed to address and resolve specific product-related or operational concerns. | 09/08/2025 |
| 590 | Novonesis Wausau, WI Assistant Application Scientist Bachelor’s degree in science related field Exp: 0-3 years |
This position works under limited supervision and is responsible for assisting in the Research and Development activities of probiotic powder formulations for encapsulation, powder filling and tableting applications. This position works directly with Product Development and Sales functions. | 09/08/2025 |
| 591 | Novonesis Morrisville, NC Research Associate I Bachelor’s degree in Biology, Microbiology, Biochemistry or related field. Exp: No exp |
We are seeking a Research Associate with a passion for hands-on research and an interest in microbial physiology or fermentation to join our Fermentation Physiology team in the Research Triangle Park, NC. In this role, you will work with a diverse team of scientists and research associates anchored in the global Microbe and Culture Research R&D organization to help in the development of biosolutions for a more sustainable world. As a Research Associate, you will leverage your laboratory skill set to plan, execute and troubleshoot experiments across our core competency areas including cell banking, microbial screening, and fermentation development. | 09/08/2025 |
| 592 | Ocular Therapeutix Bedford, MA Quality Control Chemist I/II Bachelor’s degree in Chemistry or related field Exp: 1-2 years |
Execute routine quality control testing activities as assigned by management. Support CAPA’s, change controls, investigations, and deviations. Participate in the development and validation of analytical methods for Analytical Development group. Participate in testing, project support, data review, ordering of laboratory supplies, and general upkeep of the laboratory. | 09/08/2025 |
| 593 | Orca Bio Sacramento, CA Associate, Cell Therapy Handling and Cryopreservation Bachelor’s degree in Life Sciences, Engineering, or related field Exp: 1-3 years |
The Associate, Cell Therapy Handling and Cryopreservation supports critical operations related to the receipt of patient materials (leukapheresis/blood), cryopreservation of cellular products, and preparation and coordination of final drug product shipments. This role will operate with a deep understanding of GMP manufacturing, cell therapy processes, and the ability to execute multiple tasks in a fast-paced environment. | 09/08/2025 |
| 594 | Orca Bio Sacramento, CA Cell Therapy Production Associate, Oncology (Multiple Positions) B.S. degree in Biological or related sciences Exp: 1 year |
The Cell Therapy Production Associate, Oncology plays a critical role in the production of Orca Bio’s life-saving cell therapy products, ensuring adherence to strict quality standards, regulatory requirements and aseptic production techniques. Reporting into the assigned supervisor, commercial manufacturing, the job involves repeatedly executing manufacturing processes, cleaning and maintaining production equipment and workstations and documenting production activities in a highly regulated environment. The role collaborates closely with Materials Management, Quality Control (QC), and Quality Assurance (QA) to carry out GMP manufacturing runs as part of a cross-functional team. | 09/08/2025 |
| 595 | Orca Bio Sacramento, CA Specialist, Quality Assurance Master’s degree in relevant scientific disciplines Exp: 1+ years |
The Specialist, Quality Assurance position is a key role in meeting the quality policy through their management of the different quality systems, including production records and deviation system management. The ideal candidate will be responsible for managing the quality systems, including deviations, change control, corrective and preventive actions (CAPA), and document management. Additionally, this role involves making timely batch disposition decisions to ensure quality standards are met before product release, supporting the rapid processing times required by our product. You will have the unique opportunity to make a difference in the lives of many patients as Orca Bio develops next-generation cell therapies. | 09/08/2025 |
| 596 | Orchid Orthopedic Solutions Bridgeport, MI Quality Engineer Bachelor of Science (B.S) Exp: No exp |
The Quality Engineer I supports the ongoing quality of Orchid's legacy products & processes and works cross-functionally to sustain the business. | 09/08/2025 |
| 597 | Organogenesis Canton, MA Production Associate I - Apligraf Bachelor’s degree in biology or related science Exp: 0-2 years |
This is an entry level position. The Associate will perform all activities involved in the aseptic processing of a living product (Apligraf), under the direct supervision of the Apligraf Team Leader/Apligraf Supervisor/Manager. The Apligraf Associate I will support the Apligraf Manufacturing department by performing the tasks that will assure the safe and timely processing of Apligraf, working in both a Class 100 and Class 10K cleanroom. | 09/08/2025 |
| 598 | Organogenesis Smithfield, RI Production Associate Dermagraft Bachelor’s degree in biology or related science Exp: 0-2 years |
This is an entry level position. The Associate will perform all activities involved in the aseptic processing of a living product (Dermagraft), under the direct supervision of the Dermagraft Team Leader/Dermagraft Supervisor/Manager. The Dermagraft Associate will support the Dermagraft Manufacturing department by performing the tasks that will assure the safe and timely processing of Dermagraft, working in both a ISO 7 and ISO 8 cleanrooms. | 09/08/2025 |
| 599 | Embla Medical Orlando, FL Process Improvement Specialist Bachelor’s degree in an Engineering discipline Exp: 1-3 years |
Under the supervision of their manager, the incumbent is responsible for investigation of operational improvement plans, developing, coordinating, and supporting engineering projects with many complex features. Carry out assignments requiring the development of new or improved techniques or procedures. Work on the development of new or improved techniques or procedures and new or refined equipment, materials, processes, products, and/or methods. | 09/08/2025 |
| 600 | PBL Hercules, CA In Vitro Research Assistant I/II/III Bachelor’s Degree in a science-related field (e.g., Biological Sciences, Toxicology, Pharmacology) Exp: 1-3 years |
PBL has immediate openings for a Research Assistant I/II/III in the In Vitro Services Department. The In Vitro Research Assistant is a laboratory level job focusing on the development, optimization, and execution of a variety in vitro (i.e., cell-based and noncell-based) test methods. Successful candidates will be familiar with laboratory procedures including the use of analytical balances, calculating, and preparing dilutions, pipetting, measuring pH, documenting study activities, and analyzing/interpreting data. The In Vitro Research Assistant is expected to perform under minimal supervision. Research Assistants may also contribute to general laboratory operations including equipment maintenance and maintaining a clean and organized laboratory environment. | 09/08/2025 |
| 601 | Paragon Genomics Fremont, CA Technical Operations Associate - Temporary Bachelor's degree in a relevant field (e.g. Biology, Molecular Biology, Biochemistry, Chemistry). Exp: 1+ years |
Paragon Genomics is a fast-growing life sciences company developing advanced reagents and assay kits for next generation sequencing (NGS). We are seeking a Technical Operations Associate to play an important role in the development of novel NGS target enrichment assay technologies and support current operations. This is a laboratory-based role offering strong career growth for a junior or aspiring scientist seeking hands-on molecular biology experience in the NGS field. The position provides an excellent opportunity to work in a multifaceted capacity, building a solid foundation in the biotech industry. | 09/08/2025 |
| 602 | PCI Madison, WI QA Associate I - Operations Bachelor’s degree in a relevant scientific field Exp: 0-2 years |
Join us at PCI as a Quality Associate I – Operations, where you’ll be on the front lines of GMP production—supporting real-time quality oversight, solving problems as they arise, and ensuring that every product meets the highest standards of safety, efficacy, and compliance. This is an ideal role for early-career professionals passionate about science, quality, and continuous improvement. You'll receive hands-on training, mentorship, and exposure to industry best practices while working in a fast-paced, collaborative environment. | 09/08/2025 |
| 603 | PCI Rockford, IL Project Engineer- Drug Delivery Bachelor’s degree in Mechanical, Biomedical, Chemical, or related Engineering discipline Exp: 1-5 years |
As a Project Engineer – Drug Delivery, you’ll play a hands-on, critical role in the design, development, and execution of pharmaceutical packaging and assembly projects. Working closely with engineering, quality, and validation teams, you’ll help deliver high-impact solutions that directly affect patient outcomes around the world. This role supports key product introductions - including high-speed auto-injector lines for diabetes management—giving you the opportunity to work on cutting-edge drug delivery technology. You’ll collaborate with both internal stakeholders and external customers, ensuring projects are delivered on time, on budget, and in compliance with all regulatory standards. This is more than a role—it's a career path. Our Project Engineers have advanced to senior-level roles, including Engineering Manager, based on performance, innovation, and leadership. | 09/08/2025 |
| 604 | PCI Philadelphia, PA Process Engineer I Bachelor’s degree in mechanical, chemical, biomedical, packaging engineering, or a related field Exp: 1-5 years |
PCI is seeking a motivated and detail-oriented Process Engineer I to provide technical leadership in new product launches and continuous improvement initiatives. The ideal candidate will focus on mitigating packaging issues, optimizing production processes, and supporting operational efficiency. This role will involve providing technical and operational support to production, maintenance, and support teams, particularly in the areas of process improvement, equipment modification, optimization, safety, and quality improvement. The Process Engineer I will utilize lean and six sigma techniques and demonstrate excellent organizational and leadership skills in managing projects, equipment needs, staffing projections, and line layout. | 09/08/2025 |
| 605 | Leica Biosystems Richmond, IL Lead Process Engineer Bachelor’s degree in engineering discipline or related degree Exp: 1+ years |
The Lead Process Engineer is responsible for supporting efforts to improve value stream productivity and cost of quality. This role involves coordinating with cross functional teams utilizing the Danaher Business System while maintaining high standards of quality and safety. | 09/04/2025 |
| 606 | Leidos Huntsville, AL Manufacturing Electrical Engineer 2nd shift Masters degree in electrical engineering or other engineering degree Exp: 0-2 years |
As a Manufacturing Engineer you will be overseeing and optimizing the production process, from raw materials to finished products, to ensure efficiency and quality. The type of material is expected to be electronic, electro-mechanical, and mechanical. This position will require frequent coordination with Planning & Production Control, Engineers, and Operations Leads to ensure that material will be available when needed and that proper documentation is in place for floor operations. | 09/04/2025 |
| 607 | Leidos Huntsville, AL Electrical Engineer Masters degree in Electrical Engineering, Math, Physics, or other technical degree Exp: 0-2 years |
Leidos’ Defense Systems RF Systems Portfolio is seeking an Electrical Engineer to join our team of engineers, analysts, and scientists supporting advance radar system analysis in a high-fidelity modeling and simulation environment. Our expertise is setup, test, and evaluation of radar system performance using modeling and simulation of modern air defense systems. | 09/04/2025 |
| 608 | Leidos Huntsville, AL Research Scientist Master’s degree in Electrical Engineering, Math, Physics, or other technical degree Exp: 0-2 years |
Leidos’ Defense Systems RF Systems Portfolio is seeking a Research Scientist to join our team of engineers, analysts, and scientists supporting advance radar system analysis in a high-fidelity modeling and simulation environment. Our expertise is setup, test, and evaluation of radar system performance using modeling and simulation of modern air defense systems. | 09/04/2025 |
| 609 | Leidos Charlotte, NC Transmission Line Engineer Master's degree in Civil, Structural, Electrical, or Mechanical Engineering Exp: 1+ years |
We are seeking a Transmission Line Engineer who will work as a member of a dynamic team working in a fast-paced environment, solving challenging problems involved with electric transmission. The successful candidate will serve as an Engineer on electric transmission line design projects for extra high-voltage (EHV) overhead and underground systems for some of the largest utilities in the country. This employee will apply NESC, ASCE, ACI and other applicable standards in the engineering and design of electrical overhead and underground systems, voltage conversion projects, new capacity projects, and infrastructure replacement projects. Additionally, he/she will perform engineering analyses, prepare bidding documents, draft plans and specifications, and prepare material procurement and construction documents. | 09/04/2025 |
| 610 | Leidos Beavercreek, OH Mechanical Engineer Bachelor’s degree in Mechanical Engineering or similar field Exp: 1-2 years |
This is an exciting opportunity to use your experience to advance the Air Force Research Labs (AFRL) Rapid Technology Development and Demonstrations (RTD2) program. In support of the RTD2 program, your position as a Mechanical Engineer will be to support AFRL programs mature new and emerging technologies and supporting Leidos internal research and development. The position objectives are to provide technical and operational support of new and evolving sensor systems and sensor technologies, provide support for ground and flight demonstrations and tests, and to perform sensor system integration into laboratories, aircraft, and other vehicles/platforms as necessary. | 09/04/2025 |
| 611 | Leidos Huntsville, AL Manufacturing Engineer Bachelor's degree in either Mechanical or Aerospace Engineering Exp: 0+ years |
As a Manufacturing Engineer you will be overseeing and optimizing the production process, from raw materials to finished products, to ensure efficiency and quality. The type of material is expected to be structural, mechanical, and/or electrical components. This position will require frequent coordination with Planning & Production Control, Design Engineers, Manufacturing Engineers at other sites, and Operations Leads to ensure that mBOMs are up to date, lead times are documented, and work order instructions will be available when needed and that proper documentation is in place for floor operations. | 09/04/2025 |
| 612 | Leidos Huntsville, AL Cable Manufacturing Engineer BS degree related to science and engineering (or other technical discipline) Exp: 1 year |
Leidos is seeking a talented Cable Manufacturing Engineer to join a diverse team to create unique solutions for complex problems. With offices across the United States engaging in the defense, space, cyber and commercial fields, Leidos provides responsive, cost-effective engineering, scientific and IT solutions. Candidate will develop, document, and execute manufacturing processes and procedures for cable assemblies and electromechanical products. Use of a Manufacturing Execution System (MES) will be required to create work instructions and develop build strategies. Candidate will support production of cable assemblies and electromechanical assemblies and systems. Applicant will work with a multi-disciplinary team to develop a wide variety of hardware, and work with the latest automated technology used in assembly and test equipment. | 09/04/2025 |
| 613 | LFB Charlton, MA Operations Technician - Animal Facility BS (in related discipline) Exp: 0-1 years |
Daily animal care activities to include: feeding, animal observations/identification of clinical concerns, and nail trimming. Husbandry activities to include cage change/cleaning, use of power wash and chemical dispensing equipment, and general facility sanitization and support. May perform milking of rabbits and standard support activities to meet production goals and adherence to established schedules. Proper basic restraint of rabbits to facilitate general animal care, transfers, and sample collection. Technical skills to include IP injections. May include IM, IV and SC injections. May perform animal identification applications to include ear tags, tattoos and RFID transponders. May provide support for natural and artificial insemination breeding procedures (to include restraint), and kindling/weaning procedures. Utilize computer and paper based systems to accurately document and/or record information to assure compliance with applicable regulations, and company policies. Dependent upon skill level and support needs, may provide veterinary care and animal treatments as assigned. Identify safety issues and initiate corrective actions to reach resolution. Identify and communicate animal welfare concerns. Exhibit a sound understanding of applicable animal care and use guidelines. Weekend and holiday coverage required on a rotating basis. | 09/04/2025 |
| 614 | LG GNS Evansville, IN Associate Chemist Bachelor’s Degree in Chemistry or Related Scientific Field Exp: 1+ years |
The Associate Chemist is responsible for analytical, environmental and physical testing. He or she also performs testing on raw materials and compounded products. This chemist will also participate in the development and formulation of new products under the direction of a Chemist or Senior Chemist. The Associate Chemist may provide any necessary technical support to various other departments. In addition, he or she is responsible for any other task the Chief Technology Officer deems necessary. | 09/04/2025 |
| 615 | Lonza Tampa, FL MSAT Engineer Bachelor’s degree in Science or Engineering Exp: 1-3 years |
The MSAT Engineer ensures that all GMP manufacturing processes are crafted and delivered in a compliant and efficient manner. This role supports the technical and regulatory aspects of assigned projects from inception to completion, including tech transfer and scale-up activities. The engineer collaborates cross-functionally across the organization to facilitate successful project completion aligned with Lonza’s goals. | 09/04/2025 |
| 616 | Lotte Biologics Syracuse, NY Associate Data Engineer Bachelor’s degree in Data Engineering, Data Analytics, Computer Science or related Engineering and/or Analytics Exp: 1-3 years |
The Associate Data Engineer will be responsible for supporting the organization’s data engineering activities, enterprise reporting through Microsoft Power BI, and help maintain IT/OT and data analytics applications. The ideal candidate will have experience in performing ELT/ETL processes using various data engineering tools, have a solid foundation of data warehousing concepts, and know how to build reports/dashboards using Microsoft Power BI. This is a hybrid-based position requiring employee presence, on site 50-100%. | 09/04/2025 |
| 617 | Lotte Biologics Syracuse, NY Assistant Scientist, In-Process Quality Control BS degree in a scientific field Exp: 0-3 years |
The Assistant Scientist, In-Process conducts routine general chemical and biological testing of materials and products for in-process, release and stability purpose, in compliance with all applicable procedures and regulations. A variety of duties are performed by a QC Specialist relating to the efficient and effective functioning of the Quality Control lab. | 09/04/2025 |
| 618 | Lubrizol Painesville Township, OH QC Lab Analyst Bachelor’s degree in chemistry or Related Scientific Field Exp: 1-5 years |
Performs all QC Lab activities, including but not limited to: all Standard Work Process (SWP), Management Systems, and analytical responsibilities. | 09/04/2025 |
| 619 | Mallinckrodt Raleigh, NC Chemical Process Engineer B.S. in Chemical or Mechanical Engineering Exp: 1-5 years |
The Production Engineer will function as a part of the APAP Operations Team. The Production Engineer will apply technical skills to manage day-to-day production, optimize plant operation, resolve operational issues, and investigate process deviations. The Production Engineer will provide technical assistance to the APAP manufacturing employees to ensure that production targets are met while complying with all applicable Safety and Quality rules and regulations. | 09/04/2025 |
| 620 | Mallinckrodt Fenton, MO Supv EHS B.S. degree in Chemical Engineering, Environmental Engineering Exp: 1-3 years |
The primary purpose of the Environmental Health & Safety (EHS) Supervisor is to lead the EHS function at a pharmaceutical tableting facility. Proper execution of this role will help ensure the site is a safe workplace and that it performs in a manner that meets or exceeds the company EHS strategy and expectations. The EHS Supervisor will also champion and collaborate on projects that support the goals and objectives of the site or the Company. | 09/04/2025 |
| 621 | Mallinckrodt St. Louis, MO Quality Assurance Tech II Bachelor’s degree Exp: 1-3 years |
The Quality Assurance Technician II performs a variety of review processes with the intent to correct record errors in manufacturing process documentation that includes batch record review and documentation issue resolution. This role is also responsible for return good inspections, cGMP area inspections and product inspections. This role ensures QA compliance and that cGMP principles are adhered to. | 09/04/2025 |
| 622 | Manifold Bio Boston, MA Research Associate/Senior Research Associate, In Vivo Pharmacology Bachelors or Masters Exp: 1-2+ years |
We are seeking a highly-motivated In Vivo Pharmacology Senior Research Associate who thrives in a fast-paced and creative environment to push the capabilities of our multiplexed in vivo drug discovery platform. Together with senior researchers, you will play a critical role in executing in vivo studies to support internal research projects. This is a hands-on role and you should have extensive experience in multiple aspects of in vivo pharmacology including dosing, necropsy, perfusion, tissue collection and sample processing, among others. The ideal candidate must be able to work effectively both in a collaborative setting and independently. | 09/04/2025 |
| 623 | Matica Biotechnology College Station, TX Microbiologist I, Quality Control BS/BA or greater in sciences, preferably in microbiology, biology, biotechnology, pharmaceutical sciences, or related technical field Exp: 1-2 years |
Matica Biotechnology is currently offering an excellent opportunity for a highly motivated QC professional to join our team. We are looking for someone with expertise in QC Microbiology and gene and cell-based assays preferably with cell and gene therapy experience. The Microbiologist I, QC is responsible for performing environmental monitoring in cleanrooms and for supporting QC Microbiology testing and other lab operations. | 09/04/2025 |
| 624 | Matica Biotechnology Irvine, CA Product Development Associate I Bachelor's or Master's degree Exp: 0-3 years |
The Product Development Associate I is involved in assisting with the planning, conducting and analyzing experiments leading to validation of diagnostic tests in the field of oncology. The PD Associate works in a team and needs to communicate relevant information to professional colleagues and to participate constructively in discussions that will impact the performance of the final product. | 09/04/2025 |
| 625 | Meadowhawk Biolabs Hayward, CA Reseach Associate I - In Vivo Pharmacokinetic Bachelor’s degree in biology, biochemistry, pharmaceutical sciences, or another related scientific field Exp: No exp |
Meadowhawk Biolabs is seeking a highly motivated and dynamic Research Associate to work within the Discovery In Vivo Pharmacokinetic Team at our Hayward, CA location to work with rodent models in a fast-paced team environment. The ideal candidate is driven, hardworking, willing to learn, dedicated, and passionate about science. Given that we are a newly launched Contract Research Organization (CRO) founded by an experienced team of industry veterans, this ground floor position offers unique opportunities for the successful candidate to contribute meaningfully to the creation and development of our services, expand their knowledge base by participation in multidisciplinary teams, and advance their career in capabilities and responsibilities. | 09/04/2025 |
| 626 | Meadowhawk Biolabs Marlborough, MA Research Associate II - LCMS Bachelor’s degree in chemistry, biochemistry, pharmaceutical sciences, or another related scientific field Exp: 1 year |
Meadowhawk Biolabs is seeking a highly motivated and dynamic Research Associate II to work within the Discovery Bioanalytical Team at our Marlborough, MA location to perform LC-MS/MS assays in a fast-paced team environment. The ideal candidate is driven, hardworking, willing to learn, dedicated, and passionate about science. Given that we are a newly launched Contract Research Organization (CRO) founded by an experienced team of industry veterans, this ground floor position offers unique opportunities for the successful candidate to contribute meaningfully to the creation and development of our services, expand their knowledge base by participation in multidisciplinary teams, and advance their career in capabilities and responsibilities. | 09/04/2025 |
| 627 | Medtronic Lafayette, CO R&D Engineer II Masters Degree Exp: 0 years |
In this exciting role as a Sensor R&D Engineer, you will have responsibility for designing and developing patient monitoring consumables for optical physiologic sensing applications. You will contribute across the full product lifecycle, from concept and development through design transfer and sustaining engineering. This includes creating innovative product architectures, prototyping and testing, and developing test methods and tools that ensure product performance and manufacturability. You will collaborate closely with cross-functional partners to deliver clinically meaningful, manufacturable solutions that meet customer needs. | 09/04/2025 |
| 628 | Medtronic North Haven, CT Manufacturing Engineer II Masters degree in Mechanical Engineering and/or Electro-Mechanical Engineering Exp: 0 years |
The Manufacturing Engineer II is responsible for providing daily support of multiple product families with specific regard to product quality, product cost, process development and process improvements, safety, and project management activities in procurement of new forming, grinding, laser drilling machineries, and development of manufacturing equipment validation documentations. Duties include managing and/or participating in cross functional teams to accomplish project specific goals. This position is in North Haven, CT. It is a full-time onsite position. | 09/04/2025 |
| 629 | Medtronic Minneapolis, MN Quality Engineer II Masters Degree in Engineering, Science or technical field Exp: 0+ years |
Are you passionate about ensuring the highest standards of quality in products that save and improve lives? Medtronic is seeking a Quality Engineer II to join our dedicated team at our Plymouth, Minnesota facility, where we design and manufacture mechanical heart valves—Class III Implantable Medical devices that make a direct impact on patients worldwide. This is 100% onsite role at our Plymouth, Minnesota facility. At our Plymouth site, you’ll find a collaborative, mission-driven culture where quality and innovation go hand-in-hand. You’ll work alongside talented engineering and manufacturing professionals, applying your expertise to uphold rigorous quality standards while advancing life-saving cardiovascular technology. | 09/04/2025 |
| 630 | Medtronic Minneapolis, MN Scientist II ; Neuromodulation Masters Degree Exp: 0 years |
Medtronic pioneered the field of neuromodulation with groundbreaking innovations, including the first commercially available spinal cord stimulator (SCS) for chronic pain, the first deep brain stimulation (DBS) system for movement disorders, and the first implantable drug pump for targeted medication delivery to the intrathecal space of the spine. More than 40 years later, we continue to push the boundaries of innovation, constantly challenging ourselves to disrupt the markets we created. By advancing science with bold thinking and collaboration, we bring together the right expertise to engineer groundbreaking therapies and technologies that transform patient care. | 09/04/2025 |
| 631 | Medtronic North Haven, CT Electrical Engineer - I Bachelor’s or Master's Degree Exp: 0 years |
As an Electrical Engineer 1 working on the Surgical Robotics program at the Medtronic, you will be part of a team that develops the electronic hardware for the Robotics Center of Excellence. You will work with other team members in developing, testing, integration, verification, validation, and production transfer of sophisticated electronic systems. Engineers create our market-leading portfolio of innovations. Combine the best of your experience with training and mentorship to move your career forward. If you want a challenging, energizing, rewarding career that changes lives, join us. Help us bring the next generation of life-changing medical technology to patients worldwide. | 09/04/2025 |
| 632 | Medtronic Milwaukee, WI Supplier Quality Engineer II Master's Degree in Engineering, Science or technical field Exp: 0+ years |
Medtronic – Milwaukee, WI manufactures spinal implants and Brain/ENT instrument components. As a member of Supplier Quality Engineering, you will be responsible for management of external suppliers to Medtronic, Milwaukee. You will lead oversight of supplied products, ensuring conformance to purchased material requirements and management of nonconforming product in compliance to Medtronic Purchasing and Supplier Controls, FDA, and international requirements and Quality System Regulations. | 09/04/2025 |
| 633 | Medtronic Northridge, CA Process Engineer II Master's degree Exp: 0 years |
As a member of the Medtronic Diabetes – Continuous Glucose Monitoring Sensor R&D team the Process Engineer II will support the development of next generation CGM products. This position will play a key role in the development of various new/improved chemistry layers/coatings of glucose sensors by designing and executing design feasibility, process development, and manufacturing transfer. This role will be responsible for driving the product build documentation, design and executing experiments and builds of sensors for pilot scale evaluations, execute data trending & statistical analysis. Upon successful process and design optimization, this role will subsequently support tech transfer to new product introduction and manufacturing teams. You will manage deliverables for multiple projects and maintain an effective system for tracking progress. You will be interfacing with Managers, Engineers &Technicians in R&D and New Product Introduction (NPI) Operations teams as well as Quality and Clinical groups to accomplish day to day activities. The candidate must have strong organizational skills, attention to details, an analytical mindset and ability to communicate effectively with multiple stakeholders. | 09/04/2025 |
| 634 | Molecular Designs Littleton, MA Manufacturing Test Engineer I Bachelor of Science degree in Electrical Engineering, Robotics Engineering, or equivalent Exp: 0-2 years |
The Manufacturing Test Engineer I will provide hands-on electrical engineering support for Mevion’s manufacturing operation, focused on proton therapy systems. This entry-level position involves assisting with the development and maintenance of production test setups, improving test documentation, investigating failures, and supporting continuous quality and process improvements across internal and supplier environments. | 09/04/2025 |
| 635 | Micro Systems Engineering Lake Oswego, OR Senior Engineer - Design and Development Master’s degree in Electrical Engineering, Applied Physics, or related Engineering field Exp: 6 months |
Develop, implement, and qualify new supply chain and technology platforms that enable MSEI to meet its product quality, reliability, volume, delivery, and cost objectives. Define and deploy new technology platforms in a cross-functional team for new product applications through testing, simulation, prototypes, and volume manufacturing. Use systematic problem-solving approaches to resolve quality/performance issues with suppliers, development, and manufacturing teams. Lead testing and validation of platforms for high reliability applications, by performing use case based electrical, environmental stress tests, and process limit studies. Perform implementation tasks, including leading stage-gate approvals, documentation, supplier quality interface, characterization, verification and on-going sustaining support in a highly automated manufacturing environment. | 09/04/2025 |
| 636 | Mikart Atlanta, GA Quality System Specialist Bachelor’s degree in a scientific/technical discipline Exp: 1-5 years |
The Quality Systems Specialist is responsible for the timely and accurate maintenance of vendor qualifications, complaints and adverse event investigations, and oversight of training in support of drug product development and production. | 09/04/2025 |
| 637 | Minaris Allendale, NJ QC Microbiology Analyst I BA/BS in a science or relevant field Exp: 0-2 years |
The Quality Control Microbiology Analyst I (6:30AM-5:00PM Sunday -Wednesday) serves as a support role to clinical and/or commercial production. The QC Microbiology Analyst will perform environmental monitoring activities including, but not limited to, non-viable particulate testing, active air viable, passive air viable, surface viable, and personnel monitoring. | 09/04/2025 |
| 638 | Moderna Cambridge, MA Senior Research Associate, Flow Cytometry Core M.S. in Immunology, Cell Biology, or a related life science field Exp: 0+ years |
We are seeking a highly motivated and detail-oriented Senior Research Associate to join our Flow Cytometry Core Team. The successful candidate will play a critical role in supporting method development and execution of high-throughput flow cytometry experiments, and tissue-based sample preparation. This role offers the opportunity to contribute directly to cutting-edge discovery and translational research programs through high-quality technical execution and scientific collaboration. | 09/04/2025 |
| 639 | Molecular Designs Birmingham, AL Lab Technician - Night Shift Bachelor’s degree in Biology, Chemistry, Biochemistry Exp: 6 months |
We're looking for a Molecular Lab Technician (MLT) to help with day-to-day screening procedures for our molecular testing laboratory. We’re seeking a highly driven, motivated, and experienced Lab Technician that understands the PCR process, its importance, and work through each complex step with the upmost efficiency. The ideal Lab Technician will have patience, empathy, time management, and professionalism with patients, co-workers, and providers. | 09/04/2025 |
| 640 | Moog Buffalo, NY Systems Engineer Master of Science Degree in Engineering Exp: 1+ years |
Moog is currently hiring a Systems Engineer in our Space and Defense Group. Come join a leading global supplier of motion control and electronic solutions! | 09/04/2025 |
| 641 | Lilly Lebanon, IN Manufacturing Scientist - LP1 Peptide Synthesis Master's degree in STEM Discipline (Chemistry preferred) Exp: 1 year |
The Manufacturing Scientist is part of the TSMS (Technical Services/Manufacturing Science) team that provides the technical support required to achieve reliable and compliant manufacturing of API molecules. This role will be part of the Manufacturing Process Team for its respective area, providing daily oversight to ensure safe and reliable supply of medicines. The Manufacturing Scientist executes technical projects (experimental, modeling and/or production data analysis) to improve and optimize process control, yield, purity, and/or productivity. In addition, the manufacturing scientist should be capable and of setting up and executing a variety of experiments at laboratory scale and conducting research on manufactured product for process improvements and troubleshooting in the technical services and manufacturing sciences laboratory. | 09/04/2025 |
| 642 | Lilly Lebanon, IN Sterility Assurance Scientist - Advanced Therapies Manufacturing Bachelors in Microbiology, Biology, Biochemistry, Biochemical Engineering, Chemical Engineering, or other related scientific discipline Exp: 1+ years |
Sterility Assurance – Technical Services/Manufacturing Scientist (TS/MS) role is a technical position that develops and implements the site’s sterility assurance related initiatives and provides technical leadership with regard to sterility assurance & environmental monitoring strategies. Primary objectives include the start-up and compliant manufacturing of gene therapy drug product and drug substance, particularly as it relates to development and implementation of sterility assurance strategies, including environmental monitoring, aseptic process simulations, facility cleaning, facility sanitization, and sterility assurance risk management. | 09/04/2025 |
| 643 | Lilly Indianapolis, IN Chemist, Oligonucleotide Chemistry Bachelors and/or Masters in Organic Chemistry, Chemistry, Biochemistry, or a related field Exp: 1+ years |
The Lilly Genetic Medicines Team is looking for a collaborative, creative and energetic problem solver to join a multidisciplinary team at the front edge of innovation. You will join our fast-paced, interdisciplinary team as we utilize novel RNA/oligonucleotide based therapeutic modalities to enhance the Lilly portfolio. The successful applicant will utilize their knowledge and technical expertise to accelerate the core capabilities and development of internal RNAi-based clinical candidates. | 09/04/2025 |
| 644 | Lilly Indianapolis, IN Engineer - TS/MS Device Assembly & Packaging, DPEM Bachelors Degree in Engineering (strongly preferred), Chemistry, Pharmacy or similar STEM related fields Exp: 1+ years |
This role is a member of the Technical Service Manufacturing Science function within the Drug Product External Manufacturing organization (DPEM). This role is responsible for all technical activities related to the support of external manufacturing as defined in the Global Contract Manufacturing Standards. This role is the process expert for the step(s) of the product(s) and process(es) for each contract manufacturing relationship with focus on Device Assembling and Packaging. This role is a member of the joint process team (JPT) and has direct responsibility for oversight of the day-to-day operations and technical agenda at the CM. | 09/04/2025 |
| 645 | Integer Plymouith, MN R&D Engineer I Bachelor’s degree in an engineering or related technical field Exp: 0-3 years |
The primary purpose of this position is to perform work which involves general engineering methods and tools. As an entry level engineer, you will ensure that Integer’s internal and external customer expectations are met or exceeded with the direction, instruction and guidance from more experienced engineers and managers in your organization. | 08/25/2025 |
| 646 | Integer Palm Harbor, FL Engineer I - Product Development/Design Bachelor’s degree in a related field Exp: 0-3 years |
The primary purpose of this position is to perform work which involves conventional engineering practice. Ensures Integer’s internal and external customer expectations are met or exceeded. | 08/25/2025 |
| 647 | Integra San Francisco, CA Systems Engineer I/II Bachelor’s or Master’s degree in Biomedical Engineering, Mechanical Engineering, Biochemistry, Chemical Engineering, or a related discipline Exp: 1-3+ years |
INTEGRA Microfluidics is seeking a highly motivated, hands-on Systems Engineer I/II to join our team and work on next-generation sequencing (NGS) and microfluidics projects. The successful candidate will work closely with senior engineers and scientists to develop and optimize novel microfluidic-based systems for various applications. | 08/25/2025 |
| 648 | Integra LifeSciences Plainsboro, NJ Engineer II, Continuous Improvement Masters degree in Industrial Engineering, Manufacturing Engineering, or a related field Exp: 0-2 years |
The Engineer II, Continuous Improvement will play a crucial role in driving and facilitating process improvement initiatives across the organization. This role involves analyzing current processes, identifying areas for enhancement, and implementing strategies to increase efficiency, reduce waste, and improve overall operational performance. The ideal candidate will have a solid background and understanding in process improvement methodologies, excellent analytical skills, and the ability to lead cross-functional teams. The engineer will initiate and support implementation activities for changes approved within Integra’s change management program. The Continuous Improvement Engineer II will work within cross-functional core teams on the development of new products ensuring on-time transfer of new products to production. This is an individual-contributor position. | 08/25/2025 |
| 649 | Integra LifeSciences Plainsboro, NJ Clean Room Manufacturing Operator Bachelors Degree in related science Exp: 0-2 years |
This Clean Room Manufacturing Operator role will include processes such as enzymatic treatment of collagen, alkali treatment of collagen, tendon collagen prep, dispersion preparation, and lyophilization. It is essential to perform these tasks meticulously to ensure the quality of our products. Additionally, you will be responsible for the setup, operation, and cleaning of all clean room manufacturing equipment. This entails working in ISO Class 5 or ISO Class 7 areas and adhering to Clean Room gowning protocols. All operations must be conducted in compliance with Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating Procedures (SOPs), and Health and Safety requirements. Operating in a team environment, we emphasize daily achievements and maintaining high-quality standards in our production processes. Your dedication and attention to detail will play a valuable role in our success. | 08/25/2025 |
| 650 | Integra LifeSciences Braintree, MA Sr. Manufacturing Quality Engineer l Master’s degree in science, Engineering (Biomedical or Mechanical) or related discipline Exp: 0-2 years |
This position is for a Sr. Manufacturing Quality Engineer l with hands-on experience and proven success in managing Quality systems. The successful candidate will be responsible for partnering with sterilization and microbiology Subject Matter Experts to assist in root cause investigations related to sterility and microbiological outputs, review and assess the accuracy and sustainability of process requirements as they pertain to sterility assurance and microbiology and drive cross-functional collaboration with quality groups across the organization. This role requires a strong quality mindset, a willingness to learn about sterilization and microbiology, an understanding of medical device quality systems, and a commitment to ensuring product safety and compliance. The ideal candidate should demonstrate proficient experience with quality management concepts including but not limited to eQMS, risk assessment, PFMEAs, process controls, root cause investigations, CAPA, and continuous improvement | 08/25/2025 |
| 651 | Integra LifeSciences Princeton, NJ Sr. Supplier Quality Engineer l Master's degree in engineering, or Sciences Exp: 0-2 years |
This position is for a Sr. Supplier Quality Engineer l – Global Supplier Quality with hands-on experience and proven success in managing Supplier Quality systems. The successful candidate will be responsible for partnering with sterilization and microbiology Subject Matter Experts to assist in root cause investigations related to supplied services and/or processes, review and assess the accuracy and sustainability of supplier requirements as they pertain to sterility assurance and drive cross-functional collaboration with supplier quality groups across the organization. This role requires a strong quality mindset, a willingness to learn about sterilization and microbiology, an understanding of medical device quality systems, and a commitment to ensuring product safety and compliance. The ideal candidate should demonstrate proficient experience with quality management concepts including but not limited to supplier quality audits, eQMS, risk assessment, process qualification, process controls, root cause investigations, CAPA, and continuous improvement | 08/25/2025 |
| 652 | Integra LifeSciences Plainsboro, NJ Microbiology Technician I Bachelor’s degree, in Microbiology or Biology Exp: 0-3 years |
The Microbiology Technician I will provide support to the QC Microbiology Laboratory as pertaining to the respective responsibilities. Performs functions such as executing laboratory testing for in-process and finished good products, water, stability studies, and validation studies as well as performs environmental monitoring. This position is responsible for operating in compliance with all applicable procedures and policies | 08/25/2025 |
| 653 | Integra LifeSciences Braintree, MA Quality Design and Reliability Assurance (DRA) Engineer II Master’s degree in science, Engineering (Biomedical or Mechanical) or related discipline Exp: 0-2 years |
The Quality Design and Reliability Assurance (DRA) Engineer II is responsible for the efficient and compliant support of New Product Development (NPD) and Sustaining/Remediation project(s) of varying scope and complexity in the Tissue Technology (TT) division, specifically the Boston/ Braintree site. The role contributes and supports the design and development of new and improved products. The (DRA) Engineer II will interact with external design and development partners, participating on cross-functional project teams through all phases of the product development process, and assisting the technical team with planning, executing, documenting, and communicating testing activities. The role works with Product Development, Project Management, Regulatory, Marketing and Medical Affairs. | 08/25/2025 |
| 654 | Integra LifeSciences Princeton, NJ Sr. Design Quality Engineer I Master’s degree in science, Engineering (Biomedical or Mechanical) or related discipline Exp: 0-2 years |
This position is for a Design Quality Engineer l with hands-on experience and proven success in managing Design Quality systems. The successful candidate will be responsible for partnering with sterilization and microbiology Subject Matter Experts to assist in root cause investigations related to sterility and microbiological design outputs, review and assess the accuracy and sustainability of product requirements as they pertain to sterility assurance and microbiology and drive cross-functional collaboration with design quality groups across the organization. This role requires a strong quality mindset, a willingness to learn about sterilization and microbiology, an understanding of medical device quality systems, and a commitment to ensuring product safety and compliance. The ideal candidate should demonstrate proficient experience with quality management concepts including but not limited to eQMS, risk assessment, DFMEA, process controls, root cause investigations, CAPA, and continuous improvement | 08/25/2025 |
| 655 | Integral Molecular Philadelphia, PA Research Associate Bachelor’s degree in biology, bioengineering, or a related field Exp: 1-2 years |
Perform assigned tasks in the lab, including cell culture, DNA handling, and flow cytometry in a 384-well format, as well as the associated data analysis. Operate liquid-handling robots to perform antibody stains, washes, and dilutions, while troubleshooting both experimental and equipment-related issues. Follow standard operating procedures (SOPs) to complete experiments and assays with accurate record keeping, and assist in the preparation of customer-facing reports and deliverables. Independently plan and manage a daily schedule, often balancing multiple projects simultaneously, and present experimental data at both team and company-wide meetings. | 08/25/2025 |
| 656 | Integral Molecular Philadelphia, PA Research Technician Bachelor's degree in Biology, Chemistry, medical technology or related field Exp: 6 months-2 years |
Set up and execute routine laboratory experiments, perform DNA isolation and associated quality control assays, maintain plasmid library using high throughput techniques, perform tasks using aseptic techniques including working within a biological safety cabinet, and organize large data sets within an Excel spreadsheet. | 08/25/2025 |
| 657 | Integrated DNA Technologies (IDT) Coralville, IA QA Complaint Analyst Bachelor's degree in Biological Sciences or related field (e.g., Biomedical Engineering, Systems Engineering, Pharmacology, Chemistry) Exp: 1-2 years |
This position is part of the Quality Assurance Department located in Coralville, IA and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things. | 08/25/2025 |
| 658 | Integrated DNA Technologies (IDT) Boulder, CO Manufacturing Technician II Bachelor's degree in a science related field (Biology, Genetics, Chemistry or related life science field) Exp: 1 year |
The Manufacturing Technician II is responsible for manufacturing next-generation sequencing reagents and kits, working both independently and as part of a team in concordance with established procedures and ISO 13485 guidelines. This position reports to the Manufacturing Supervisor and is part of the xGen Manufacturing team located in Boulder, Colorado and will be an on-site role. | 08/25/2025 |
| 659 | IMI Pompano Beach, FL Engineer I Bachelor’s degree in mechanical engineering, or equivalent Exp: No exp |
Engineer I is the entry level engineering position for product development. The Engineer will work under the direct supervision of a manager and/or more experienced team members, to design, prototype, inspect and test specific components and assemblies of a medical device, while creating & maintaining compliant documentation for tasks preformed. The position is intended to prepare engineers new to the medical device industry for advancement to the next level of Engineer II. | 08/25/2025 |
| 660 | Inventprise Woodinville, WA Manufacturing Associate I - 1st Shift Bachelor’s degree Exp: 0-3+ years |
The Manufacturing Associate I is responsible for executing and monitoring manufacturing processes on the plant floor. They are also learning and becoming familiar with navigating Inventprise Quality Systems and will provide information to help support the reporting of administrative and compliance related tasks including: nonconformance investigation and report writing, generation and execution of CAPAs, and revision and creation of batch records and standard operating procedures. | 08/25/2025 |
| 661 | Inventprise Woodinville, WA Manufacturing Associate I - 2nd Shift Bachelor’s degree Exp: 0-3+ years |
The Manufacturing Associate I is responsible for executing and monitoring manufacturing processes on the plant floor. They are also learning and becoming familiar with navigating Inventprise Quality Systems and will provide information to help support the reporting of administrative and compliance related tasks including: nonconformance investigation and report writing, generation and execution of CAPAs, and revision and creation of batch records and standard operating procedures. | 08/25/2025 |
| 662 | Invivoscribe San Diego, CA Quality Control Laboratory Associate I B.S. degree in a scientific discipline Exp: 0-2 years |
We are looking to add a Quality Control Laboratory Associate I is responsible for ensuring that only quality products are released for distribution. It is a QCLAI’s job to ensure that products are tested to meet the applicable government regulations and industry standards, and to maintain GMP environment. The Quality Control Laboratory Associate is also responsible for data entry. | 08/25/2025 |
| 663 | IQVIA Ithaca, NY Scientist, Lab Operations Bachelor's degree in applied/laboratory sciences Exp: 0-2 years |
We are seeking a Scientist, Lab Operations to join Q2 Solutions, IQVIA’s laboratory business at Ithaca, NY. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Join our scientific team to execute laboratory procedures and contribute to research excellence while maintaining compliance with GLP standards. You’ll play a key role in analyzing data and supporting projects that impact global health. | 08/25/2025 |
| 664 | IQVIA Durham, NC Clinical Research Associate, Obesity/Diabetes/GLP-1 (Full Service) Bachelor's Degree in scientific discipline or health care Exp: 1 year |
IQVIA is hiring a Clinical Research Associate with on-site monitoring experience in GLP-1/Obesity/Diabetes (Type II) clinical trials. Phase 1 experience is a plus! Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. | 08/25/2025 |
| 665 | IQVIA Ithaca, NY Associate Scientist, Sample Preparation Bachelor’s Degree in a Life Sciences discipline Exp: 6 months |
We are seeking an Associate Scientist to join IQVIA Laboratories in Ithaca, NY. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Responsible for routine sample preparation duties inclusive of troubleshooting routine experiments and the preparation of solutions and reagents. | 08/25/2025 |
| 666 | IQVIA Valencia, CA Laboratory Technical Specialist Bachelor's Degree in life sciences or other relevant field Exp: 1 year |
We are seeking a Laboratory Technical Specialist to join Q2 Solutions, IQVIA’s laboratory business at Valencia, CA We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. You will lead the production and development of specialized reagents for digital ELISA assays, collaborating cross-functionally to drive product transfer and support diagnostic assay manufacturing. This is a fully on-site position. | 08/25/2025 |
| 667 | IQVIA Indianapolis, IN QA Auditor 1 Bachelor’s degree Exp: 1 year |
We are seeking a QA Auditor 1 to join Q2 Solutions, IQVIA’s laboratory business at Indianapolis, IN. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Support quality assurance efforts by assisting in the coordination, documentation, and execution of audits under the direction of senior QA staff. This role ensures regulatory compliance and strengthens operational excellence within a dynamic laboratory setting. | 08/25/2025 |
| 668 | Johnson & Johnson Santa Clara, CA R&D Project Manager I (Sustaining) - Shockwave Medical BS/BA in science, engineering Exp: 1-2 years |
The R&D Project Manager I is responsible for managing PMO initiative projects by coordination of cross functional project activities to ensure projects achieve desired outcomes. Under guidance and direction, this role will be responsible for supporting the successful implementation of best practices throughout the project lifecycle. | 08/25/2025 |
| 669 | Johnson & Johnson Raritan, NJ GTO Associate Pkg Development Engineer Bachelor’s Degree in Package Engineering or Technical Degree (Mechanical, Chemical, Biomedical Engineering, etc.) Exp: 0-2 years |
The Primary Engineer will be designing, developing and testing sterile barrier packaging systems for J&J Medtech at Ethicon Inc. This role will support both New Product Development and Lifecycle Management teams. | 08/25/2025 |
| 670 | J-STAR Research Cranbury, NJ Research Scientist Master in Chemistry, Chemical Engineering, Pharmaceutical Chemistry, or Food Science Exp: 1 year |
Pharmaceutical Ingredient (API), intermediates, impurities, starting material and excipients from drug substances and drug products. Analyze organic and inorganic compounds to determine chemical or physical properties, composition, structure, relationships, reactions, using chromatography, spectroscopy, spectrophotometry techniques including HPLC, UPLC, IC, GC, MS, UV, XRPD, DSC, TGA, NMR, and KF. Design and perform method verification and validation. Determine the specificity, linearity, accuracy, precision, forced degradation, robustness of the methods. Collect and analyze data, and maintain data integrity under GMP, GLP, and FDA regulations. Prepare documentation of test procedures and technical reports. Prepare, review, and/or approve methods, protocols, and development reports. Maintain laboratory instruments to ensure proper working order. Apply scientific expertise to troubleshooting, laboratory investigation and problem resolution. Participate in maintaining high quality laboratory environment and comply with Health, Safety and Environmental responsibilities for the position. | 08/25/2025 |
| 671 | J-STAR Research Cranbury, NJ Research Scientist of Crystallization R&D MS or BS. in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related field Exp: 1-5 years |
We are seeking a highly motivated and skilled Research Scientist to join our Crystallization R&D Department at Porton J-STAR. In this role, this position is responsible for leading group or contributing individually to conduct Solid Form Studies and pre-formulation will search for the right solid form and develop formulations to support preclinical and Phase I studies including PK, PD, efficacy, tox studies. This role is also responsible for Crystallization Process Development will develop crystallization processes to define and control final solid form of drug substances with desired solid-state attributes needed for optimum performance as well as drug intermediates for robust purification. The responsibilities of the position include, but are not necessarily limited to, the items listed below. | 08/25/2025 |
| 672 | Jubilant HollisterStier Seattle, WA Weekend Shift Process Engineer I, II, III, & Sr. Bachelor’s of Arts or Science with a major in Biology, Chemistry, Physics, or Engineering Exp: 0-5 years |
The weekend shift Process Engineer I/II/III/Sr. provides ownership and focus for pharmaceutical processes and technical transfers at Jubilant HollisterStier. This position will engage in and manage projects and multi-disciplinary teams with direct supervision. The process engineer will also contribute technical direction for complex projects and exhibit clear communication skills with all levels of employees. | 08/25/2025 |
| 673 | Jubilant HollisterStier Spokane, WA Manufacturing Specialist Bachelors Exp: 1-5 years |
The Manufacturing Specialists direct train schedule and coordinate daily production within multiple areas of Raw Materials department. Ensure technician training is completed in a timely manner, perform technician training and review documentation. Ensure all resources and supplies are available for day-to-day operations. | 08/25/2025 |
| 674 | Jubilant HollisterStier Spokane, WA Microbiologist I/II Bachelor of Science in Microbiology or related hard science with microbiology emphasis Exp: No exp |
The QC Microbiologist I/II performs the microbial analysis on allergenic and client components, raw materials, intermediates, and finished products following written procedures, providing the data required to determine raw materials/product disposition. | 08/25/2025 |
| 675 | Jubilant HollisterStier Spokane, WA Environmental Monitoring Specialist Bachelors of Science Exp: 1 year |
The Environmental Monitoring Specialist performs the functions associated with sampling, initiating tests, collecting and evaluating test results related to defined quality parameters for surface, air, personnel, product and utility systems such as compressed gases and WFI. The Specialist oversees EM functions and personnel, schedules projects, tasks and personnel, assists in training EM technicians and gown training of all aseptic personnel. | 08/25/2025 |
| 676 | KBI Biopharma Durham, NC Microbiology Associate I/II Bachelor’s/Master’s degree in Microbiology, Biology or related technological field of science Exp: No exp |
Testing and support for the Microbiology Laboratory in support of a Contract Manufacturing biotechnology facility and Process Development. Responsibilities includes laboratory support, program testing, reporting of results, execution of protocols. This person is responsible for the aspects of the following programs as directed by management: Environmental Monitoring (Air Viable, Total Air Particulate, Surface Viable); Clean Utility Monitoring (Water Sampling, Bioburden, Conductivity, TOC, Coliform and Nitrates); Compressed Gas Monitoring (Collection, Air Viable, Total Air Particulate, Dragger Tests and specific ID tests); Product Testing (Bioburden, Endotoxin, Host Purity, or Non-Host); Media Release; Laboratory Support. It is the expectation that this position is required to be onsite full time. Addition, this position should be in the laboratory/facility for a minimum of 75% time daily. Second Shift: Sunday - Wednesday [2:00 PM EST - 12:00 AM EST]. | 08/25/2025 |
| 677 | KBI Biopharma Durham, NC Downstream Manufacturing Associate I/II Bachelor’s degree in a related scientific or engineering discipline Exp: 0-2 years |
The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Manufacturing Associate must follow written, approved procedures and forms to ensure all work is conducted “Right First Time” (RFT) following Good Manufacturing Practice (GMP), including good documentation practices, and/or Good Laboratory Practice (GLP). As needed, the Manufacturing Associate will work individually or on teams to author standard operating procedures (SOPs) or Master Batch Records (MBRs); write corrective and preventive actions (CAPAs); and specify, commission, and qualify new equipment. | 08/25/2025 |
| 678 | KBI Biopharma Durham, NC Manufacturing Associate l/ll Bachelor’s degree in a related scientific or engineering discipline Exp: 0-2 years |
The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Manufacturing Associate must follow written, approved procedures and forms to ensure all work is conducted “Right First Time” (RFT) following Good Manufacturing Practice (GMP), including good documentation practices, and/or Good Laboratory Practice (GLP). As needed, the Manufacturing Associate will work individually or on teams to author standard operating procedures (SOPs) or Master Batch Records (MBRs); write corrective and preventive actions (CAPAs); and specify, commission, and qualify new equipment. | 08/25/2025 |
| 679 | KBI Biopharma Durham, NC QA Specialist I- Quality Engineering Bachelor’s degree Exp: 1-3 years |
The Manufacturing Quality Assurance (MQA) Specialist is responsible for supporting the Manufacturing Process and Areas as part of a rapidly expanding GMP Contract Manufacturing Organization. MQA Specialists are expected to provide sound guidance to Manufacturing with respect to process, SISPQ of product, and risk. MQA Specialists share responsibility for the inspection readiness of the site. MQA Specialists routinely work on the cleanroom floor directly with the Manufacturing team to provide real time guidance and support. Specialists routinely collaborate with Manufacturing and work on team initiatives. The MQA Specialist may also be responsible for coaching and mentoring as needed to foster a GMP compliant site. | 08/25/2025 |
| 680 | KBI Biopharma Durham, NC Research Associate II Master’s degree in chemistry, biochemistry or related area Exp: 0+ years |
Join a highly technical analytical team in a dynamic work environment where you will participate in contracted client analytical programs as a member of the Analytical Development (AD) Department. The individual in this position will be responsible for executing experimental protocols and performing data analysis in biopharmaceutical laboratories. | 08/25/2025 |
| 681 | Kindeva Bridgeton, MO Quality Engineer Master’s degree in a scientific or engineering discipline Exp: 1-3 years |
In this role, you will develop, direct, and lead Quality oversight for process improvements in equipment and material preparation, aseptic compounding, filling, inspection, and packaging at the Brentwood, Maryland Heights, and Bridgeton facilities. You will coordinate support activities, reviews, audits, and the release of semi-finished products and components to align with site-wide objectives. You will collaborate with cross-functional teams to support continuous improvement initiatives, incident investigations, and change management. Additionally, you will make decisions related to Incident Investigations and Corrective and Preventive Actions, ensuring a focus on overall quality, site priorities, and operational success. | 08/25/2025 |
| 682 | Kindeva Woodbury, MN Product and Process Development Scientist Bachelor’s degree in a science discipline Exp: 1 year |
This is an exciting role within an expanding team of process and product development specialists and offers the successful candidate an opportunity to make a significant contribution to the development of new inhalation products. The person hired for the position of pMDI Product and Process Development Scientist will support the development and testing of pMDI pharmaceutical products. | 08/25/2025 |
| 683 | Krystal Biotech Pittsburgh, PA Clinical Trial Associate/Clinical Research Coordinator BS/BA degree required in science/health-related field Exp: 1-3 years |
Krystal Biotech, Inc. is seeking a Clinical Trial Associate to support our Clinical Operations Team. The Associate's responsibilities will entail, but not be limited to, assisting with the management and inventory of clinical supplies, ensuring proper materials are available at clinical sites in a timely manner, and working with the Clinical Operations team to support multiple Clinical Trials. Conducting reviews of trial data and follow GCP/ICH protocols/guidelines. Will require travel to Clinical sites, including up to 50% of the time, during peak periods. | 08/25/2025 |
| 684 | Krystal Biotech Moon Township, PA Bioprocess Engineer Bachelor’s degree, preferably in life sciences Exp: 1+ years |
Krystal Biotech, Inc is seeking a highly motivated and dynamic Bioprocess Engineer to support our product manufacturing at our Pittsburgh GMP facility. This role is critical to our make a meaningful difference in the lives of underserved patient populations having rare diseases. Quality, safety and on-time delivery is a must to be successful in this role! The ideal candidate will have foundational experience in upstream and/or downstream biologics or gene therapy manufacturing. | 08/25/2025 |
| 685 | Getinge Wayne, NJ Quality Systems Data Analyst Bachelor’s Degree in Engineering, Data Analytics, or related field Exp: 1-3 years |
We are seeking a results-driven and detail-oriented Data Analyst to support our Quality organization. This hybrid role plays a key part in driving data-informed decision-making and leading strategic quality initiatives across the organization. The ideal candidate will analyze quality data trends, lead process improvement projects, and ensure compliance with applicable medical device regulations and standards. The position supports the Cardiac Surgery business and is a hybrid role with a minimum of 3 days onsite at the Wayne, NJ headquarters. | 08/19/2025 |
| 686 | Getinge Wayne, NJ Engineer I, Production Bachelor’s degree in Manufacturing/Industrial, Mechanical, Biomedical Engineering or Instrumentation (Electrical Engineering) Exp: 1-2 years |
Supports production area in tooling design, process improvement, and cost improvement. | 08/19/2025 |
| 687 | Gilead Foster City, CA Sr Research Associate, Medicinal Chemistry Masters degree Exp: 0+ years |
As a Sr. Research Associate, you will participate a multi-disciplinary drug discovery team through the design and synthesis of new molecules. The successful candidate will have an excellent track record and a commitment to tackling drug discovery challenges through organic synthesis. | 08/19/2025 |
| 688 | Gilead Foster City, CA Research Associate, Medicinal Chemistry Bachelors degree Exp: 0+ years |
As a Research Associate, you will participate on a multi-disciplinary drug discovery team through the design and synthesis of new molecules. The successful candidate will have an excellent track record and a commitment to tackling drug discovery challenges through organic synthesis. | 08/19/2025 |
| 689 | Gilead Foster City, CA Sr Research Associate, Drug Metabolism MS degree in pharmacology, pharmaceutical sciences, cell biology, biochemistry, or relate Exp: 0+ years |
The primary responsibility of the Drug Metabolism and Pharmacokinetic (DMPK) Senior Research Associate role is to conduct absorption, distribution, metabolism, and excretion (ADME) studies to support the discovery and development of drugs candidates. As a member of the DMPK department, the candidate will conduct laboratory experiments (biochemical or cell-based) and bioanalysis (LC/MS and other methods), interpret data, and contribute to understanding of the ADME properties of small molecules. | 08/19/2025 |
| 690 | Gilead Oceanside, CA Senior Research Associate, Biologics Pivotal Formulation & Process Development MA / MS Degree in Pharmaceutical Science, Chemistry, Biochemistry, Chemical Engineering, or related scientific fields Exp: 0+ years |
We are seeking a highly motivated, attentive, and self-driven candidate to join our team, Biologics Pivotal Formulation and Process Development, as a Senior Research Associate. Once onboarded, the successful candidate will contribute in developing formulation and drug product processes for innovative molecules. The candidate will have tremendous opportunities for career growth in a fast-paced and resource-rich environment through training and professional relationships. The ideal candidate is expected to be action oriented with high expectations of themselves and others. S/he should have good verbal and written communication interpersonal skills. | 08/19/2025 |
| 691 | Gilead Foster City, CA Research Associate, Analytical Ops BS or BA degree in Chemistry, Biology or relevant science/engineering majors Exp: 0-2 years |
We are seeking a highly motivated, attentive, and self-driven candidate to join the Method Validation and Transfer team in Global Small Molecules. The successful candidate will contribute to the method validation of drug substance, drug product intermediate and drug product to support early phase clinical projects. The candidate will have opportunities for career growth through acquisition of new skills, experiences, and GMP knowledge in a fast-paced and resource-rich environment. The ideal candidate is expected to be action oriented and should possess good verbal and written communication and interpersonal skills. | 08/19/2025 |
| 692 | Globus Medical Audubon, PA Associate Project Engineer - Sustaining Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, or a related field Exp: 0-3 years |
Design and implement product line extensions, working closely with the R&D, clinical, and regulatory teams. Champion Design for Manufacturing (DFM) improvements across launched product lines to optimize cost, reliability, and manufacturability. Resolve manufacturing challenges through vendor coordination and iterative design updates. Provide technical support during cadaver labs and customer engagement meetings to validate and refine device performance. Support surgical cases in the operating room, working directly with surgeons to gather real-time feedback and identify clinical opportunities for improvement. Perform product scrap analysis and coordinate remediation strategies to improve yield and performance. Conduct complaint evaluations, identify root causes, and implement corrective actions in collaboration with cross-functional teams. Lead and contribute to Post-Market Surveillance Reports (PMSR) and Periodic Safety Update Reports (PSUR) in compliance with global regulatory standards. Drive risk analyses to assess and mitigate design and process risks. | 08/19/2025 |
| 693 | Globus Medical West Carrollton, OH Manufacturing Engineer Masters degree in an engineering discipline Exp: No exp |
As a Manufacturing Engineer, you will develop, implement and maintain methods, operation sequence and processes in the manufacture or fabrication of parts, components, sub-assemblies and final assemblies. Support new initiatives and productivity targets for given manufacturing processes. Interface with design engineering in coordinating the release of new products. Estimate manufacturing cost, determine time standards and make recommendations for tooling and process requirements of new or existing product lines. Maintain records and reporting systems for coordination of manufacturing operations. | 08/19/2025 |
| 694 | Globus Medical Audubon, PA Regulatory Associate Bachelor’s degree in health or science-related field, or equivalent; Engineering degree is a plus Exp: 0-2 years |
The Regulatory Affairs Associate assists in drafting, submitting and gaining clearance for 510(k) submissions, and approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products. This position entails development of FDA submissions, requiring working knowledge of products under review and of relevant regulations and guidance documents. This individual must be enthusiastic, positive, even-tempered and effective in building working relationships with internal teams while following FDA 21 CFR regulations. | 08/19/2025 |
| 695 | GRAM Grand Rapids, MI QC Chemist I (1st shift/Group B) Bachelor’s degree in Chemistry and/or other related discipline (e.g. Biochemistry, Biotechnology) Exp: 1-3 years |
The QC Chemist supports quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties include, but are not limited to, providing general laboratory support for raw material, in-process, stability, and finished product testing. | 08/19/2025 |
| 696 | GRAM Grand Rapids, MI Finishing Shift Lead (2nd shift) BS or BA in Biopharmaceuticals, or other Life Sciences field Exp: 1 year |
Do you exhibit these values and wish to be around others that do too? Do you thrive in fast-paced environments where agility, adaptability, and high standards go hand in hand? Are you driven to make a meaningful impact, whether through your work, your support of others, or your commitment to your community? Are you motivated by a disciplined, science-based approach that ensures consistent excellence, safety, and integrity in everything you do? If these statements resonate with you, Grand River Aseptic Manufacturing (GRAM) welcomes you to apply to join our community of dedicated individuals improving lives every day! | 08/19/2025 |
| 697 | GRAM Grand Rapids, MI QC Microbiology Technician (2nd shift) Bachelor’s degree in Microbiology or a related field Exp: 0-2 years |
The QC Microbiology Technician supports quality control and assurance by assisting the microbiology department with environmental monitoring, water testing, and client specific testing. | 08/19/2025 |
| 698 | GRAM Grand Rapids, MI QC Microbiology Technician (3rd shift) Bachelor’s degree in Microbiology or a related field Exp: 0-2 years |
The QC Microbiology Technician supports quality control and assurance by assisting the microbiology department with environmental monitoring, water testing, and client specific testing. | 08/19/2025 |
| 699 | GRAM Grand Rapids, MI QC Chemist I (2nd Shift/Group A) Bachelor’s degree in Chemistry and/or other related discipline (e.g. Biochemistry, Biotechnology) Exp: 1-3 years |
The QC Chemist supports quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties include, but are not limited to, providing general laboratory support for raw material, in-process, stability, and finished product testing. | 08/19/2025 |
| 700 | GRAM Grand Rapids, MI Environmental Health & Safety Specialist I or II Bachelor’s or Master's degree Exp: 0-3 years |
The Environmental Health & Safety (EHS) Specialist I or II works with EHS Department to review and interpret regulatory requirements, relating to EHS, and provide cost effective recommendations to the EHS Manager for implementation and compliance. The EHS Specialist I performs a variety of complex tasks and assist in the work of others. The EHS Specialist II performs a variety of complex tasks and may lead and direct the work of others. A fair degree of creativity and latitude is expected with either the level I and/or level II role. This is an on-site position. | 08/19/2025 |
| 701 | Grifols Clayton, NC Assistant/Associate/Senior Biologist BS/BA degree in a life science field, medical technology, or related Exp: 6months |
The incumbent is responsible for performing complex laboratory analysis of plasma and plasma products in a GMP laboratory. Responsibilities include sample accessioning, sample preparation, reagent preparation, testing, result calculation, as well as quality control of assays and equipment. The incumbent will also support assay validation, method transfer, reagent and control qualification, and laboratory maintenance activities as assigned. Must be comfortable working with infectious material on a daily basis. Person must be able to work in a biological safety cabinet and comfortable working with a microscope for several hours at a time. Candidates for the position must be proficient with using micropipettes and serological pipettes while making dilutions and serial dilutions. Must be able to perform tasks by following SOP’s and oral instructions. Must have precise, legible, and organized documentation skills. Candidates must also be willing to perform their share of cleaning duties and housekeeping. | 08/19/2025 |
| 702 | Grifols Clayton, NC Engineer - Validation I Bachelors Degree in Engineering Exp: 0-2 years |
The Engineer I - Validation / Engineer II – Validation / Validation Specialist I / Validation Specialist II / Sr. Validation Specialist I position supports Fractionation, Purification, Filling, Utilities and/or capital projects as required. This position is responsible for assigned qualification and validation related activities related to supporting the Clayton NC site. | 08/19/2025 |
| 703 | GSK Cambridge, MA Associate Scientist Analytical Chemistry MS Exp: 1+ years |
As Associate Scientist/Sr. Associate Scientist, Analytical Chemistry, you and your team will play an important role in the analysis and quality control of GSK’s preclinical pipeline. You will maintain and troubleshoot analytical equipment and execute diverse analytical methods for small molecules and oligonucleotides to help accelerate GSK’s pipeline and platform technology ambitions. | 08/19/2025 |
| 704 | Guardant Health Redwood City, CA Biospecimen Associate I Bachelor of Arts or Science in Biomedical Laboratory Science, Clinical Science or related field Exp: 1-2 years |
The Biospecimen Associate I supports the management of patient samples and provides the link between the Clinical Operations and Client Services teams. The Biospecimen Associate I is responsible for receiving, unpacking, processing, and recording samples sent for laboratory testing under the supervision of the Biospecimen Management Supervisor. The Biospecimen Associate I has demonstrated an understanding of laboratory workflow. | 08/19/2025 |
| 705 | Hikma Pharmaceuticals Dayton, OH Quality Assurance Associate Bachelor’s Degree in Science Exp: 1-2 years |
Under the supervision of the Quality Assurance Supervisor, this person is responsible for performing field QA activities: in process checks in the aseptic processing area, approval for area clearance, AQL inspection for finished products, retention sampling for finished products, batch record review, final product release, review and approve operation documents and forms, and approval / rejection of in-coming raw materials, components, and final product labels. Ensure compliance of operations personnel with the company’s procedures and Good Manufacturing Practices (GMPs). This position will also be responsible for identifying any deviations or non-conformances, writing deviation reports, performing root cause analysis, writing/revising standard operating procedures and forms, and tracking metrics, when required. | 08/19/2025 |
| 706 | Hikma Pharmaceuticals Cherry Hill, NJ QA Inspector Bachelor’s Degree Exp: 0-2 years |
We continue to be committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated QA Inspector, QA. In this role, you will be responsible for monitoring in-process product quality for Filling and Inspection and Packaging of parenteral products. The QA Inspector is responsible for performing visual and functional testing of product against statistically based sampling plans. In addition, the QA Inspector performs routine inspection and testing of components in accordance with Standard Procedures and specifications as required by production scheduling. In performing the above duties, the individual is responsible for accurately and clearly documenting test results in accordance with cGMPs. This position participates in rotation for weekend coverage and as needed during the work week. | 08/19/2025 |
| 707 | Hologic Newark, DE Electrical Engineer 3 Bachelor’s or Master's degree Exp: 0-3 years |
The Electrical Engineer 3 designs, develops, modifies and evaluates components and processes used in the generation, manipulation, transmission and storage of electricity. Determines design approaches and parameters. Analyzes equipment to establish operating data, conducts experimental tests and evaluates results. Selects components and equipment based on analysis of specifications and reliability. Completes documentation and procedures for installation and maintenance. May interact with users to define system requirements and/or necessary modifications. Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors. Demonstrates good judgment in selecting methods and techniques for obtaining solutions. Networks with senior internal and external personnel in own area of expertise. A seasoned, experienced professional with a full understanding of area of specialization; resolves a wide range of issues in creative ways. This job is a fully qualified, career-oriented, journey-level position. Normally receives little instruction on day-to-day work, general instructions on new assignments. | 08/19/2025 |
| 708 | Hologic Newark, DE Sr. Quality Assurance Engineer Master’s Degree in Electrical Engineering Exp: 1-3 years |
Are you a quality-focused professional passionate about ensuring excellence in manufacturing and production processes? Join Hologic as a Senior Quality Assurance Engineer and play a critical role in designing, implementing, and maintaining quality assurance protocols that meet internal and external regulatory standards for worldwide distribution. In this role, you’ll collaborate with cross-functional teams, lead quality initiatives, and drive continuous improvement to ensure the delivery of high-quality, innovative products that improve lives globally. | 08/19/2025 |
| 709 | Humacyte Durham, NC 2D Bioprocessing Associate I Bachelor’s degree Exp: 0-1 years |
The Bioprocessing Associate I participates in the hands-on production of Humacyte’s regenerative vessels. | 08/19/2025 |
| 710 | Hyperfine Guilford, CT Regulatory Affairs Associate Bachelor’s or Master'sdegree in a scientific or regulatory discipline Exp: 6 months-1 year |
As our Regulatory Affairs Associate, you will be an individual contributor responsible for analysis, evaluation, preparation, and submission of documentation for regulatory approval, ensuring Hyperfine products and procedures comply with US and global regulatory specifications. You will support our Regulatory team across different program areas, and will work on multiple projects concurrently. | 08/19/2025 |
| 711 | ICON Wilmington, NC Staff Scientist - Drug Metabolism and Biotherapeutics (DMB) Bachelor’s degree in biology, Life Science, or related discipline Exp: 0-3 years |
As a Staff Scientist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. The Staff Scientist in Drug Metabolism and Biotherapeutics (DMB) will support research projects by helping plan and carry out in vivo pharmacokinetics studies. In this role, you’ll prepare doses, coordinate study schedules, and handle general lab tasks. You’ll also have the opportunity to cross-train and gain experience with in vitro assay support. | 08/19/2025 |
| 712 | ICON Wilmington, NC Chemical Library Specialist BS in Chemistry/Life Sciences or related field Exp: 0-3 years |
As a Chemical Library Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. In this role, you will contribute to the development and expansion of our internal high-throughput screening chemical library, supporting the discovery of new therapeutic entities. This position offers an exciting opportunity to apply your chemistry expertise in a dynamic laboratory environment. The successful candidate will play a key role in a variety of departmental initiatives and laboratory-based tasks, gaining hands-on experience in cutting-edge discovery chemistry projects. | 08/19/2025 |
| 713 | Illumina San Diego, CA Facilities Engineer 2 Master’s degree in Industrial Engineering, Mechanical Engineering, Electrical Engineering Exp: No exp |
The Facilities Engineer 2 will be part of the San Diego Facilities Engineering team. This role will be responsible for providing technical expertise as related to mechanical and electrical systems within facilities equipment engineering, support maintenance, and/or calibration and equipment performance optimization. Including projects related to mechanical, electrical, and plumbing (MEP) systems in an FDA regulated environment. The individual will possess technical knowledge of facilities water purification (RO/DI) skids, HVAC, chillers, centralized gas distribution systems, walk-in cold storage units, clean rooms, BMS/EMS system, Electrical generation and distribution system for Low, Medium and High Voltage, and other plant utilities, facilities validation, as well as construction management skills. | 08/19/2025 |
| 714 | Illumina Remote, OR Field Service Engineer 1 Bachelor’s degree in Electrical/Electronics Engineering, Mechanical Engineering, or a related field Exp: 1-3 years |
The Field Service Engineer plays a critical role in delivering exceptional on-site technical support for Illumina’s cutting-edge products. This position serves as a key liaison between customers and internal teams, ensuring optimal performance and satisfaction through expert service and support. | 08/19/2025 |
| 715 | Immunai New York, NY Associate Scientist, Molecular Profiling BS degree in Biology or related field Exp: 1-2 years |
The successful candidate will work in a fast-paced team alongside highly experienced scientists and will interface closely with a multidisciplinary team of immunology, molecular biology, and bioinformatics scientists. Specifically, they will contribute to the Molecular Profiling team performing high throughput profiling of clinical and experimental samples using flow cytometry, bulk RNA-seq, dissociated and spatial single cell multiomics. The successful candidate will be an excellent team player, agile in thought, energetic, and willing to learn new methods and skills. | 08/19/2025 |
| 716 | InBios International Seattle, WA Quality Engineer I (In Vitro Diagnostics) Master's degree in chemical, mechanical or bioengineering, or related discipline Exp: 1+ years |
As a Quality Engineer I, you’ll be instrumental in upholding the quality and compliance of our in vitro diagnostic products. You’ll collaborate with cross-functional teams to ensure our assays meet regulatory standards, perform reliably, and are safe for clinical use. Your strong organizational and communication skills will help foster a culture of quality and continuous improvement across the organization. | 08/19/2025 |
| 717 | INCOG BioPharma Fishers, IN Manufacturing Specialist - Formulation BS in biological sciences/biotechnology or related field Exp: 1 year |
INCOG BioPharma is seeking a highly motivated individual with subject matter expert (SME) capabilities in the formulation of sterile drug products. The Manufacturing Specialist (Formulation) is a key role within INCOG BioPharma Operations. The ideal candidate must have experience in pharmaceuticals and/or biologics formulation. The primary responsibility of the Manufacturing Specialist in Formulation is to weigh/dispense, setup/operate equipment to produce the bulk drug product for sterile manufacturing. They will be expected to work hands-on, be actively involved in continuous process improvements while taking ownership of the quality and quantity of product produced. The ideal candidate should demonstrate mentor and leadership skills to motivate manufacturing personnel, drive timely production activities and work effectively with internal partners, clients, and vendors. | 08/19/2025 |
| 718 | INCOG BioPharma Fishers, IN Manufacturing Specialist- Filling BS in biological sciences/biotechnology Exp: 1 year |
INCOG BioPharma is seeking a highly motivated individual with subject matter expert (SME) capabilities in sterile pharmaceutical manufacturing process controls and industrial automation. The Manufacturing Specialist is a key technical role within INCOG BioPharma Operations. The ideal candidate must have experience in pharmaceuticals and/or biologics, GMP manufacturing, or within highly regulated industries. | 08/19/2025 |
| 719 | Indee Labs Berkeley, CA Scientist, Immunology Masters Exp: 1-3 years |
We are seeking a Scientist or Senior Scientist, Immunology to join the team full time to accelerate the biological development of Hydropore at our Berkeley office. Indee Labs is headquartered in Berkeley, CA and accommodates remote work. This position will be located in Berkeley, CA and occasional work travel may be required. | 08/19/2025 |
| 720 | Indee Labs Berkeley, CA Senior Bioengineer Masters Exp: 1-3 years |
We are seeking a Bioengineer or Senior Bioengineer, Immunology to join the team full time to accelerate the biological development of Hydropore at our Berkeley office. Indee Labs is headquartered in Berkeley, CA and accommodates remote work. This position will be located in Berkeley, CA and occasional work travel may be required. | 08/19/2025 |
| 721 | Indee Labs Berkeley, CA MEMS Engineer Masters Exp: 1-3 years |
We are seeking an MEMS Engineer or Senior MEMS Engineer to join the team full time to accelerate the development of Hydropore in our Berkeley office. Indee Labs is headquartered in Berkeley, CA and accommodates remote work. This position will be located in Berkeley, CA and occasional work travel may be required. | 08/19/2025 |
| 722 | Indica Labs Albuquerque, NM Field Applications Scientist Bachelor’s Degree in Biology or related biomedical science Exp: 1 year |
Hybrid sales and technical position which provides Applications Support and some Sales Support in digital pathology and image analysis for Indica Labs' HALO, HALO Link, and HALO AI platforms in a commercial, educational, or research environment. | 08/19/2025 |
| 723 | Indivior Raleigh, NC MQA Specialist Bachelor’s degree in science, engineering field, or equivalent Exp: 1-3 years |
The Manufacturing Quality Assurance (MQA) Specialist is responsible for providing quality oversight to all manufacturing areas to ensure product quality and SOP/GMP compliance. The MQA Specialist will work closely with production personnel to complete in-process batch record review, resolve batch related issues, and ensure proper good documentation practices. In addition, the MQA Specialist will be responsible for performing routine environmental monitoring to assess the viable and nonviable particulate levels within classified manufacturing rooms and support rooms. | 08/19/2025 |
| 724 | Insmed Bridgewater, NJ QA Product Quality Complaint Specialist BS in engineering, Life Science or related discipline Exp: 1-2 years |
Reporting to the Director, Product Quality Complaints, the Product Quality Complaint Associate, QA will play a key role in the complaint process. Specific areas of responsibility include: Ensure accurate and thorough complaint intake information, replacement need, trouble-shooting with complainant, patient follow-ups, product complaint investigations, tracking and trending of complaint data. The position is based in our Bridgewater, NJ HQ (onsite 3 days a week). | 08/19/2025 |
| 725 | DWK Life Sciences Rockwood, TN Mechanical Engineer Bachelor’s Degree in Mechanical or Materials Science & Engineering Exp: 1+ years |
Creative leader with an entrepreneurial vision to develop new and improved cutting-edge products/processes as required by current and future clients. Subject Matter Expert in applying Engineering Disciplines to effectively manage projects from ideation to completion. Will work in a fast-paced production environment and apply creative thinking to develop and design mechanical solutions to improve production efficiency and reduce scrap. | 08/13/2025 |
| 726 | Element Fort Wayne, IN Microbiologist Bachelor's or Masters Degree in Microbiology Exp: 1-2 years |
Element has an opportunity for a Microbiologist to join our growing team in Fort Wayne, IN. The primary responsibility of the Microbiologist is to support laboratory operations by conducting the relevant microbiological testing. | 08/13/2025 |
| 727 | Element Santa Fe Springs, CA Quality Specialist I Bachelor’s degree in Chemistry, Biology, Pharmaceutical Sciences, or related field Exp: 0-2 years |
Element has a current opening for a Quality Specialist I to join our growing team in Santa Fe Springs, CA. The Quality Specialist I supports the Quality Assurance function by performing routine QA activities to ensure compliance with applicable regulatory requirements (e.g., FDA 21 CFR Part 11, 210/211, ISO 17025) and internal quality standards. This entry-level position assists with reviewing analytical data packages, monitoring compliance in laboratory activities, equipment and method qualifications review and approval, and document control. Reports to the Quality Supervisor and/or Quality Manager. | 08/13/2025 |
| 728 | Element Wixom, MI Corrosion Technician Bachelor's degree Exp: 1-2 years |
Element has an opportunity for a Test Technician (Corrosion) to join our rapidly expanding team in Wixom, MI. Primary responsibilities include a variety of routine and non-routine testing assignments to assist the Corrosion Testing department. The technician must insure timely and accurate test results with minimal direct supervision. | 08/13/2025 |
| 729 | EMD Electronics Tempe, AZ Senior Research Chemist Master’s Degree in Physics, Chemistry, or other science discipline Exp: 1+ years |
In this role you will work within the Analytical Technology group for the analysis and characterization of CMP slurries for the semiconductor fabrication industry. | 08/13/2025 |
| 730 | Endo Rochester, MI Chemist II Master’s Degree in chemistry, chemical engineering or related field Exp: 1+ years |
The Chemist II, under general supervision, performs QC laboratory chemical analyses of raw materials, in-process materials, stability & finished products, and testing to support process validation. Detects, participates and reports on OOS/OOT/NOE and other investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. May train less senior staff. | 08/13/2025 |
| 731 | Enovis Austin, TX Promade Product Development Engineer - Upper Extremities Masters degree Exp: No Exp |
Manages a specific product or group of products from product definition and planning through production and release. Responsible for coordinating employee recruitment, selection and training, performance assessment, work assignments, salary, and recognition/disciplinary actions. Directs interfaces with central resource in design, process, manufacturing, test, quality, and marketing as the product(s) move to completion and distribution. Manages production support engineering with respect to testing methods, procedures, and problems; device specification and yield problems; redesign of devices; analysis of customer returns; and optimization of device production relative to cost constraints. Serves as adviser to sales force and customers on all matters concerned with designated products. Recommends product program development and/or enhancements as a result of customer and/or sales force feedback. | 08/13/2025 |
| 732 | Enplusone Biosciences Watertown, MA Research Associate - Synthesis Bachelor’s degree in Molecular Biology, Biochemistry or Chemistry Exp: 1 year |
Your primary role as a Research Associate on the Synthesis team at EnPlusOne is to support the enzymatic RNA synthesis platform. You will assist staff scientists in RNA synthesis, reaction screening, data analysis, buffer preparation, QAQC, and inventory. You will work on multiple internal projects and external collaborations. You will be expected to keep a well-documented lab notebook, stay highly organized, use good communication, and collaborate well with our awesome team. Successful candidates are self-starters who are endlessly curious, excited by research, and flexible in a fast-paced, constantly evolving field. | 08/13/2025 |
| 733 | Eurofins Andover, MA Particle Characterization Scientist BS in Pharmaceutics, Chemistry, Chemical/Biochemical Engineering, Pharmacy, Biochemistry, Bioengineering, Biotechnology, Biology or equivalent Exp: 1+ years |
The incumbent will participate in the formulation and process development of biotherapeutics. This position will be responsible for performing particle characterization of candidate molecules by using various biophysical, biochemical and particulates characterization techniques as well as supporting laboratory operations and maintenance. This is a laboratory-based position performing formulation and process development activities specifically for biotherapeutic products from pre-clinical and Ph I clinical trials through late stage, license application and commercialization. Furthermore, this position will assist in data compilation, data presentations, report authoring, and department documentation support. | 08/13/2025 |
| 734 | Eurofins Lancaster, PA Associate Scientist, Biochemistry Bachelor's degree in chemistry or other related degree concentration Exp: Entry level |
Perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products (tablets, capsules, parenterals, devices, aerosols, liquids, creams, and gels). Run the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, IR, ICP, AA, TGP, DSC, PDA, auto-titrators, TLC, and dissolution apparatus. Preparing samples for analysis and running some instrumentation with minimum supervision. Set up and validate new analytical or related processes used by the department. Prepare standards and samples for analysis. Execute method transfer protocols. Document work as required for GMP compliance. Perform monthly maintenance of laboratory equipment | 08/13/2025 |
| 735 | Eurofins Boston, MA Analytical Chemist M.S. in Analytical Chemistry, Biochemistry, Chemistry, or a related field Exp: 1 year |
This role supports analytical method development and data generation to inform product development, with cross-functional collaboration and a strong emphasis on scientific rigor, safety, and continuous improvement. | 08/13/2025 |
| 736 | Eurofins Malvern, PA Laboratory Operations Support (Project Management) BS/MS in a scientific field Exp: 1-5 years |
Initiate continuous improvement initiatives for Asset management and laboratory Operations and update impacted procedures. Maintain and support best business practices for Asset management such as Share Point Asset management. Work with managers, coordinators, and staff of labs to resolve instrumentation documentation issues. Work with QA and compliance to initiate, investigate, and resolve quality issues. Review QA’s monthly overdue work order list and research instrument service history and use to resolve documentation issues. Review training documents to see which are coming due for their 3-year update. Verify CAR-T data for regulatory submission and make SharePoint updates. Verify regulatory submission needed, and make Share Point updates. Facilitate change control closure and send out notifications to activity owners and approvers. Make status updates to change control SharePoint. Work directly with vendors to resolve instrumentation accuracy and inventory documentation issues. Support inventory accuracy for laboratories in Malvern and Spring House sites. Update Maximo/eCMMS to address inventory inaccuracies, and maintain eCMMS system’s accuracy. Provide process improvement and instruction to decrease turn-around time for bringing instruments into service. Research asset history for resolution of outstanding work orders. | 08/13/2025 |
| 737 | Eurofins Tustin, CA Chemist I - GCMS (Multiple Shifts) Eurofins Environment Testing BS or BA in chemistry or related field Exp: 1+ years |
Eurofins Environment Testing Southwest- Tustin CA is searching for a SVOA GCMS Chemist I to prepare and analyze environmental samples following EPA protocols in adherence with Eurofins Quality Assurance programs and SOP’s. | 08/13/2025 |
| 738 | Eurofins Lexington, MA Upstream Development Engineer Bachelor’s degree in chemical engineering, biochemistry, engineering or related pharmaceutical science Exp: 0+ years |
The Upstream development engineer will work primarily with scientists/senior research associates or engineers in the upstream fed-batch culture process development team to design and optimize consistent cell culture processes that produce quality recombinant proteins through laboratory studies. Additionally, as a fundamental component related to cell culture process design and development, the process development team will also ensure that these processes are predicable, scalable, and controlled with multiple size of bioreactors (ambr15, ambr250 and bench-top scale bioreactors). The position is to support tech transfer of developed/locked cell culture processes to pilot team and CMOs. | 08/13/2025 |
| 739 | Eurofins St. Charles, MO Associate Scientist – Cell Culture B.A./B.S./M.A./M.S. Degree in the life science field Exp: 0-2 years |
Performs work in a laboratory setting, meeting the physical job requirements of a lab role. Prepares and manages inventory of buffers, reagents, media, semi-finished and finished goods. Maintains cell culture in a BSL2 laboratory, and adheres to cleanroom guidelines and aseptic technique, according to protocols. Adheres to department SOPs and documentation requirements, maintains accurate data management and reporting. Generates data by performing lab assays in Ion Channel Services and other business units as needed. Conducts production assays with recombinant, primary and traditional cell models used in human tissues to cells and cell-based bioassays. Understands and complies with requirements for work performed at a GxP site. Completes required training and supports 100% of Employee Health and Safety requirements. Demonstrates proficiency with, care, and maintenance of lab equipment and department assets. Conducts responsible use of confidential IT and business systems, as required. Supports unit goals and demonstrates Eurofins’ competencies, as defined in the job plan. Provides training to colleagues and external end users, when required. Contributes to scientific community, and site research and development objectives. Works effectively in a team environment, under minimum direction, to achieve business production, project timelines, and quality objectives. Adjusts work hours and provides cross-functional support to other departments, as required, and maintains accountability in delivering to client needs/timelines. Routinely communicates project updates to internal and external clients. Performs other duties, as assigned. | 08/13/2025 |
| 740 | EvolveImmune Branford, CT Senior Research Associate, Immunobiology Master’s degree in Immunology or a related field Exp: 1-3 years |
We are seeking a creative and technically strong immunology-focused discovery scientist to join our Immunobiology team. The ideal candidate will have expertise in T cell engager biologic functional assessment, including tumor killing, cytokine production, T cell exhaustion assays, and multiparameter flow cytometry immune cell analysis. Experience in T cell engager discovery, particularly in evaluating CD3 bispecifics or costimulatory biologics, is preferred. The successful candidate will contribute to the discovery and assessment of novel costimulatory T cell engagers to determine key differentiation design features and supporting mechanisms of action. This includes designing and performing functional assays to prioritize alternative protein designs based on tumor killing potency, cytokine release and immune modulation mechanism of action. Collaboratively design in vivo proof of principle studies to test in vitro-driven hypothesis on molecule prioritization, mechanism of action, lead assessment, and selection of preclinical models to evaluate immune pharmacodynamic and establish in vivo mechanisms of differentiation. They will also work closely with our biotherapeutics and in vivo pharmacology research teams to drive T cell engager platform discoveries to drug development programs. Strong verbal and written communication skills are necessary, as is a proven track record of scientific and project achievements in biopharma. We are looking for a candidate who thrives in a collaborative, team-oriented environment and is eager to leverage the growth opportunities within a matrixed organization. This is an exceptional opportunity for a scientist passionate about T cell engager platform discovery and driven to translate innovative research into novel therapeutics. | 08/13/2025 |
| 741 | Evonik Birmingham, AL Plant Engineer I BS/MS in an engineering field including but not limited to Mechanical, Electrical, Industrial, Chemical, or Biomedical Engineering Exp: 1-3 years |
The Plant Engineer I acts as system owner and subject matter expert (SME) for assigned area(s) to include but not limited to infrastructure, utilities, and process equipment. He/ She will ensure that the assigned systems are in a state of operational readiness by ensuring that preventive maintenance is carried out on time and in full, any issues are documented and investigated, corrective and preventive actions are implemented. He/ She provides technical expertise to maintain and continuously improve assigned areas to improve reliability, reduce downtime, minimize costs and ensure technical means for safe and high-quality operation. | 08/13/2025 |
| 742 | Exact Sciences Madison, WI Laboratory Service Technician IV Bachelor’s degree in Engineering, Technology, Molecular Biology, Electronics, or related field Exp: 1+ years |
The Laboratory Service Technician IV is responsible for the Instrument Services of laboratory equipment and instrumentation, including installation, calibration, maintenance, and repair. This includes both simple (e.g., orbital shakers) and complex (e.g., liquid handling robotics.) instrumentation in the various laboratory environments. These environments may include clinical laboratories, R&D laboratories, and manufacturing and quality control laboratories. The individual in this role will continuously work with other Lab Service Technicians and the laboratory teams to ensure proper instrument function and to troubleshoot any system concerns. The LST may work continuously with other technicians and the laboratory teams to ensure proper instrument function and to troubleshoot any system concerns. | 08/13/2025 |
| 743 | Exact Sciences Phoenix, AZ Quality Control Associate I Bachelor’s degree in Clinical Laboratory Science or Medical Technology or in the chemical or biological sciences Exp: 1+ years |
The Clinical Laboratory Quality Control (QC) Associate (Tues - Sat and Sun - Thurs 10:00am - 6:30pm) performs and functions within the Technical Laboratory under the guided direction of the Supervisor, Clinical Laboratory Quality Control Lead, or designee. In this support position, the Clinical Laboratory QC Associate ensures daily QC operations are effective and efficient by coordinating with leadership to anticipate and resolve issues related to efficiencies in quality control, and laboratory processes. | 08/13/2025 |
| 744 | Exactech Gainesville, FL Continuous Improvement Engineer Bachelor’s Degree in a related field Exp: 1-3 years |
The Continuous Improvement Engineer will be responsible for developing and sustaining performance management systems, lean manufacturing practices, and continuous improvement initiatives across operations, fulfillment, and other departments as needed. This role will focus on optimizing workflow, improving material and information flow, and implementing standardized work at all levels. The Industrial Engineer will play a key role in fostering a culture of continuous improvement (CI) and data-driven decision-making within the organization, ensuring compliance with ISO 13485 and other relevant regulations. | 08/13/2025 |
| 745 | Exactech Gainesville, FL Manufacturing Engineer Bachelor's degree Exp: 1-3 years |
Create and maintain the lowest cost, highest quality machining & manufacturing processes, tooling and supporting documentation for all parts produced. | 08/13/2025 |
| 746 | Exelixis Alameda, CA Scientist III, Discovery Oncology MS/MA degree in related discipline Exp: 1 year |
The successful and highly motivated candidate will work to identify the mechanism(s) of action of small molecular agents in cellular systems, evaluate the activity of small molecules in cell-based assays for oncology drug discovery, and help to enable new technologies for drug discovery efforts in cell models. Comfortable in a dynamic and energetic team-based environment, the ideal candidate will actively contribute to develop cell-based functional assays and problem resolving, reliably execute experiments, interpret and analyze results. Good lab practicing and multitasking are required. This job will require the candidate to have good organization, communication and teamwork skills as well as flexibility and versatility to meet deadlines. | 08/13/2025 |
| 747 | Fagron Wichita, KS QC Technician - Chemist I Bachelor’s degree in a science field Exp: 0-2 years |
The Quality Control Technician supports the Quality Control department by assisting with analytical testing, mainly for product release. | 08/13/2025 |
| 748 | Flamma Group Malvern, PA Associate Process Scientist BS or MS in Organic Chemistry Exp: 0-1 years |
Execute laboratory experiments. Assist in determining operational space for various process parameters to ensure efficient and successful scale up. Help evaluate safety of processes utilizing calorimetry data and stability data to fully understand the hazards and the trigger points of these hazards. Follow guidance from senior scientists or project leader to problem solve complex synthetic problems during development. Assist in scale up of processes in the kilo labs. Support scale up of processes in the pilot plant in a GMP environment. Collaborate with analytical chemists to complete work assignments. Contribute to laboratory organization (daily weigh checks, update of lab supplies inventory, lab supply purchase, lab cleaning, equipment calibration). Accurately collect reliable data in the form of lab procedure or reports to be used for updates to customers or during drafting of production’s MBR. | 08/13/2025 |
| 749 | Fluke Everett, WA Test Engineer I Bachelor's degree in Electrical Engineering Exp: 0-2 years |
Do you thrive in a fast-paced environment? Are you a self-starter who finds ways to improve existing processes? We are looking for a dynamic Test Engineer I to join our Fluke Electronics team here in Everett, WA. As a Test Engineer I, you will be tasked with analyzing, developing, implementing, and maintaining methods, manufacturing operation sequences, specifications, and equipment requirements for the production assembly of new and existing products. You will assist with new product introductions to manufacturing and provide ongoing product support. Through these activities, you will improve metrics in areas such as safety, quality, cost, and productivity. | 08/13/2025 |
| 750 | Fresenius Kabi Wilson, NC Scientist I B.S. in Chemistry, Biology or related physical science Exp: 1-4 years |
A Scientist I in Quality Control is responsible for an intermediate level of expertise in analytical chemistry, chromatographic methods of analysis and instrumentation, including troubleshooting. Directs and provides guidance to associate scientists. | 08/13/2025 |
| 751 | Frontage Laboratories Hayward, CA Research Assistant BS or MS in biology, chemistry, or related area Exp: 0-2 years |
This position will support experiment design, data collection, analysis, troubleshooting, and data reporting within the DMPK department. This includes gathering data on pre-clinical compound parameters using a variety of techniques, organizing and processing the data using statistical and analytical methods to reach meaningful conclusions, and reporting observations to clients and other decision-makers. | 08/13/2025 |
| 752 | Frontage Laboratories Exton, PA Scientist Genomics Bachelor’s or Master’s degree in Molecular Biology, Genetics, Biotechnology, or a related field Exp: 0-2 years |
We are seeking a detail-oriented and highly collaborative Scientist to join our Genomics team. This is an excellent opportunity for an early-career scientist to gain hands-on experience in a fast-paced environment supporting a wide range of client-driven studies. The successful candidate will have a solid foundation in molecular biology techniques such as PCR and nucleic acid handling, and excels in documentation, communication, and collaborative work. | 08/13/2025 |
| 753 | Frontage Laboratories Chicago, IL Research Technician BS degree in animal/veterinary science, biology, or related disciplines Exp: 0-3 years |
The Associate/Assistant Toxicologist plays a key, hands on role in the conduct of preclinical studies and supports the Study Director to ensure that Sponsor studies are conducted properly and according to FDA guidelines. | 08/13/2025 |
| 754 | Frontage Laboratories Concord, OH Associate Scientist I Bachelor’s degree in biology, microbiology, toxicology, chemistry, or a related scientific field Exp: 0-2 years |
We are seeking a motivated, detail-oriented individuals to join our GLP-compliant Genetic Toxicology Laboratory in Concord, OH. This full-time, on-site Associate Scientist-I role involves supporting in vitro and in vivo genetic toxicology assays, including bacterial reverse mutation assay (Ames Assay), in vitro Micronucleus Assay using using human lymphoblastoid (TK6) cell line and human peripheral blood lymphocyte (HPBL), and rodents in vivo Micronucleus assay, Comet Assay, and Pig-a assay. The successful candidate will be properly trained to perform hands-on laboratory procedures following study protocols, SOPs, and regulatory standards, contributing directly to data quality and compliance. | 08/13/2025 |
| 755 | FUJIFILM Biotechnologies College Station, TX Manufacturing Technician III, Solution Prep Bachelor’s degree in Biology, Microbiology, Chemistry, Biochemistry, Engineering, or other related field Exp: 1 year |
The Manufacturing Technician III will work directly with a range of technologies. Dependent upon assignment, the range of technologies exposed to will be: Preparation of medium from stock raw materials including the compounding, mixing, testing and filtration for further process needs. Preparation of buffers from stock raw materials including the compounding, mixing, testing and filtration for further process needs. Weighing of raw materials per batch record specifications and assignment of appropriate expiry per procedures. Integrity testing of filters. Write and review standard operating procedures, buffer formulation records and batch production records. Assist senior staff in implementing project safety and quality assurance programs in accordance with SOPs. Maintain the confidentiality of proprietary company information. Document and maintain activity records according to cGMP regulations and ensure junior team members are trained. Operate general production equipment such as Autoclaves, Glass washers, Incubators, Analytical Scales, pH/conductivity meters, etc. Perform daily cleaning and sanitization of the laboratory and manufacturing areas. Maintain an effective working relationship with others. Perform all other duties as assigned. | 08/13/2025 |
| 756 | FUJIFILM Electronic Materials Mesa, AZ New Product Introduction Engineer - Pilot Plant BS degree in Chemical or Mechanical Engineering Exp: 0-2 years |
The Pilot Plant Lab Engineer supports process development and the production of low-volume products. Key responsibilities include performing SAP transactions, contributing to CIP projects, conducting Engineering Reviews, and managing equipment. Additionally, the role involves collaborating within the team and across departments to achieve project goals effectively. | 08/13/2025 |
| 757 | FUJIFILM Electronic Materials Mesa, AZ Quality Assurance Engineer Bachelor’s degree in Chemical Engineering, Chemistry, Industrial Engineering or Quality Engineering Exp: 1-2 years |
The Quality Assurance Engineer is responsible for executing and improving key QMS processes to drive improvements in FEUS processes and product quality, at a pace consistent with the needs of our strategic customers. | 08/13/2025 |
| 758 | FUJIFILM Biotechnologies Holly Springs, NC Sr. Analyst 1, QC Chemistry (Routine Testing) B.S. in Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field Exp: 1-3 years |
The QC Chemistry Sr. Analyst 1 works with limited direction to execute QC analytical chemistry methods used in biological product manufacturing, including chromatography, spectroscopy, electrophoresis, wet chemistry, glycan analysis, sub-visible particle analysis, peptide mapping, and physical appearance, etc. The QC Chemistry Sr. Analyst 1 adheres to GMP-compliant laboratory operations in accordance with regulatory guidelines. This role generates analytical results and identifies laboratory exceptions, invalid assays, deviations, change controls, and corrective and preventative actions (CAPAs). The role is primarily responsible for executing routine analytical methods in support of manufacturing, supporting laboratory execution of analytical method transfers and validations, and training other QC Chemistry laboratory associates. The ability to effectively communicate and function in a fast-paced, highly technical environment is essential to success. | 08/13/2025 |
| 759 | FUJIFILM Biotechnologies Holly Springs, NC Engineer / Scientist 2/3, Downstream - MSAT Master's degree in Engineering, Life Science or Chemical Engineering Exp: No exp |
The Engineer / Scientist 2/3, Downstream MSAT will provide tech transfer support and technical oversight for large scale purification activities for Monoclonal antibody production. | 08/13/2025 |
| 760 | Gameto New York City, NY Scientist I – Biomaterials Master’s degree in chemical engineering, biomedical engineering, materials science, chemistry, or a related field Exp: 1-2+ years |
In this position, you will serve as a key contributor to the design and optimization of bioengineered delivery platforms that form part of Gameto’s menopause implant program. Your work will directly support our mission to advance women’s health and contribute to Gameto’s core technology platform. We are looking for a self-motivated, technically skilled individual who enjoys working in a fast-paced, cross-disciplinary environment with evolving priorities. | 08/13/2025 |
| 761 | Genezen Lexington, MA MFG Specialist II - Compliance Master’s degree Exp: 1-2 years |
The MFG Specialist in this role will be part of a cohesive team responsible for Deviation investigations, CAPAs, and Change Controls for all phases of manufacturing. The Manufacturing Specialist uses expert knowledge of cGMP regulations and project management to ensure manufacturing readiness and compliance. The incumbent will also support equipment, documentation and process operations improvement initiatives within Manufacturing. The MFG Specialist works independently with minimal supervision and direction. Performs work that consistently requires independent decision making and the exercise of independent judgment and discretion. | 08/13/2025 |
| 762 | Genezen Indianapolis, IN Microbiology Technician B.S. degree in a scientific/technical discipline Exp: 1+ years |
Microbiology Technician is responsible for Environmental Monitoring (EM) and Personnel Monitoring for pharmaceutical cleanrooms and the associated spaces including general microbiology laboratory responsibilities. The Environmental Monitoring (EM) technician ensures strict adherence to all cGMP/GMP policies and standard operating procedures and communicates effectively with other departments. The position requires working independently, but also under the supervision of the QC Microbiology management. This is a contract-to-hire position. As a contract employee, you will not be eligible for company benefits until you are converted to a full-time, regular employee. | 08/13/2025 |
| 763 | Genezen Lexington, MA QC Analyst - Microbiology (Contract) BA or BS in Microbiology or other related science Exp: 0-3 years |
The QC Analyst contract role will be responsible for routine and non-routine QC sampling and testing for the quality of products manufactured for our clients. QC is responsible for execution of the Environmental Monitoring (EM) program in place to monitor Genezen's controlled manufacturing environments (cleanrooms) as well as monitoring of utility systems including Water for Injection (WFI), Pure Steam, Purified Water, Compressed Air and Gas systems. These activities are all performed in accordance with cGMP guidelines and are supported by departmental and interdepartmental policies and standard operating procedures (SOPs). This position is based at Genezen’s state-of-the-art facility in Lexington, MA. This role supports daily operations as well as occasional weekend and holiday operations. This may include but is not limited to in-process monitoring and testing, lot release testing, and stability testing. Supporting activities for quality systems: utility monitoring excursions, non-conformance, deviations, corrective and preventive actions (CAPAs), investigations, Out of Specifications (OOS), and change controls may be required. | 08/13/2025 |
| 764 | GenScript Biotech Corporation Pennington, NJ Associate Scientist, Microbiology Bachelor’s degree in Microbiology, Biology, Biochemistry or related scientific field Exp: 0-2 years |
The position reports to the Manager of Microbiology, is ideally suited for a professional with technical knowledge, and a proven track record of developing and carrying out processes, that are suitable for use in GMP manufacturing of a wide range of clinical trial materials, and participating in the technology transfer. There is a great opportunity to learn this function within a CDMO business, to support a broad portfolio and advance the manufacturing capabilities to deliver products to the client projects that transform the lives of patients. | 08/13/2025 |
| 765 | Celularity Morristown, NJ Operator, Clinical Manufacturing B.S degree in Biology, Bioengineering or related scientific discipline Exp: 1-2 years |
Celularity is seeking a dynamic individual to join a motivated team of clinical operators for the daily manufacture of multiple cell therapy products in support of clinical stage platforms and collaborations. Leveraging Celularity’s state-of-the-art cGMP capable facility, this position will make use of existing innovations and future technologies to meet and exceed manufacturing demand. | 08/05/2025 |
| 766 | Celularity Morristown, NJ Sr. Research Associate, Medical Devices, Research & Development B.S. in Bioengineering, Biology, or related discipline Exp: 1-3 years |
The Senior Research Associate is responsible for day-to-day analytical/biophysical testing and process development activities, supporting the company’s product development and commercial needs. This position will play a key role in the development and validation of innovative placenta-derived biomaterial medical devices or cell-based products, contribute to cross-functional R&D efforts driving regulatory submissions and operate at the interface of biomaterials, process development, product testing, and regulatory compliance to ensure robust product performance. This role involves developing and validating analytical/biophysical assays and testing product prototypes in compliance with regulatory requirements and industry standards. Furthermore, this role will conduct process development, validation, documentation and transfer to manufacturing activities relevant to medical devices, cell therapy or exosome products. | 08/05/2025 |
| 767 | CenExel Anaheim, CA Clinical Research Coordinator Bachelor's Degree Exp: 1+ years |
Responsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies. | 08/05/2025 |
| 768 | CenExel Garden Grove, CA Clinical Research Coordinator III Bachelor's Degree Exp: 1+ years |
Responsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies. | 08/05/2025 |
| 769 | Centogene Miami, FL Lab Technician (m/f/d) Bachelor’s degree in Molecular Biology, Genetics, Biomedical Science, or a related field Exp: 1-2 years |
Receive and verify biopsy samples from embryology labs. Perform DNA amplification, whole genome amplification (WGA), and library preparation for next-generation sequencing (NGS) in accordance with standard protocols. Operate and maintain lab equipment such as thermocyclers, centrifuges, and NGS platforms (e.g., Iontorrent; Illumina). Ensure accurate tracking of samples using laboratory information systems (LIS). Validate inputs, equipment and new protocols in accordance with the laboratory guidelines. Adhere strictly to laboratory quality control and quality assurance standards. Assist with data entry, documentation, and review of test results under supervision of clinical supervisors or geneticists. Maintain a sterile and compliant work environment following CLIA/CAP/ISO standards. Participate in validation and proficiency testing as required by accreditation bodies. Communicate effectively with embryologists, clinicians, and laboratory staff to ensure sample integrity and result accuracy. Present in front of customers, like a Scientific Advisor, attend conferences and write abstracts for those conferences | 08/05/2025 |
| 770 | Centrillion Palo Alto, CA Laboratory Technician B.A./B.S. in a molecular biology, genetics, or microbiology Exp: 6 months |
We are looking for a Laboratory Technician to join our R&D team in Palo Alto. The role is part of a small group that divides their focus between innovative new projects and product development. The ideal candidate will be extremely organized, familiar with basic laboratory techniques, and excited to learn and grow within the team. Technicians will divide their time between hands-on laboratory work, data analysis, and lab organization and maintenance. Candidates with knowledge and experience of PCR, library preparation, NGS sequencing or RNA seq will be given preference. | 08/05/2025 |
| 771 | Charles River Rockville, MD Biomanufacturing Associate II B.S. in biology/life sciences, bioengineering, or related discipline Exp: 1-2 years |
This role will apply solid knowledge and experience across a range of tasks, in resourceful and effective ways, requiring good judgment and initiative, when effectively executing manufacturing protocols. | 08/05/2025 |
| 772 | Charles River Wilmington, MA Laboratory Technician – MDX B.S. in biological sciences or related discipline Exp: 1 year |
Performs technical laboratory activities in support of client studies or procedures. Records data in compliance with company and regulatory policies and standards to meet quality and accuracy requirements. Reconciles customer paperwork with submission documentation to ensure accuracy. Makes detailed observations and maintains documentation of all laboratory work. | 08/05/2025 |
| 773 | Charles River Rockville, MD QC Micro Associate I – Environmental Monitoring B.S in Biology or related field Exp: 1-2 years |
At Charles River Laboratories, we are looking for a highly motivated and energetic candidate to join our growing business in the CMO industry. The QC Analyst I will perform microbiological testing, static and dynamic viable and non-viable monitoring of classified clean room areas to support planned or in process manufacturing processes. This position, as well as all positions in the Charles River team will require demonstration of Charles River DNA “Characteristics and Behaviors” (Care, Lead, Own and Collaborate). | 08/05/2025 |
| 774 | Charles River Ashland, OH Senior Associate Scientist – Principal Investigator(Bioanalytical Chemistry) M.S./M.A. in a scientific related discipline Exp: 1-3 years |
Serve as a scientist in the conduct of assigned nonclinical research studies of basic complexity, to include study management, interpretation, and reporting of study data, and assuring the regulatory compliance of these projects. | 08/05/2025 |
| 775 | Charles River Mattawan, MI Senior Associate Scientist, Project Scientist – Large Molecule Bioanalysis Master’s degree Exp: 1-2 years |
The Immunology and Immunochemistry disciplines support large molecule drug development using ligand binding assays, such as enzyme-linked immunosorbent assay, to measure large molecules and their immune responses. The main types of assays include Pharmacokinetic assays to measure drug and Immunogenicity assay to measure anti-drug antibodies and neutralizing antibodies. Other assay types also performed are branched DNA and cell-based assays. An array of platforms are used to support these assays that include spectrophotometer, Meso Scale Discovery, Luminex and Gyrolab. Utilizing these platforms/assays, the teams are responsible for the method development, validation and routine sample analysis in both the regulated and non-regulated space of non-clinical and clinical studies. | 08/05/2025 |
| 776 | Charles River Cleveland, OH Research Analyst I - Manual Ion Channel Testing Bachelor’s degree (BA/BS) Exp: No exp |
The Manual Ion Channel Testing group is responsible for evaluating test article effects on ion channels in vitro. Personnel are responsible for operating and maintaining manual patch clamp electrophysiology workstations. Validated hardware and software systems are used to collect and analyze data under regulated (GLP) or non-regulated conditions. The group prepares, collects and transfers test article formulation samples to the CLE analytical chemistry unit (or other appropriate laboratory) for concentration verification and homogeneity analyses, and is responsible for interpretation and reporting of data outcomes. | 08/05/2025 |
| 777 | Charles River Cleveland, OH Research Analyst I – Bioanalytical Chemistry Bachelor’s degree (BA/BS) Exp: No exp |
Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP’s and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents. | 08/05/2025 |
| 778 | Cipla Hauppauge, NY QA Validation DHF - DPI Bachelor's degree in scientific discipline (e.g., biology, chemistry, pharmacy) or a related field Exp: 1-2 years |
Responsible for the coordination of supportive equipment and process validation activities such as testing, calibration, scale-up, engineering and validation studies, and assurance that the necessary project documentation is complete, accurate and in compliance with cGMP regulations. | 08/05/2025 |
| 779 | Cipla Fall River, MA Quality Assurance Analyst I Bachelor's or Masters degree in Chemistry. Pharmaceutical Sciences, or related field of study Exp: 1-3 years |
The Analytical Quality Assurance (AQA) associate I position is an team contributor role and reports to the Supervisor Analytical Quality Assurance for InvaGen Pharmaceuticals, Inc., a Cipla subsidiary located at Fall River, MA. | 08/05/2025 |
| 780 | Cipla Central Islip, NY QC Chemist I Master's degree in chemistry, pharmaceutical or related field Exp: 1+ years |
Demonstrated ability to perform independent work requiring attention to detail, accuracy and scientific judgment and a consistent record of shifting thought processes quickly from one task to another. Strong analytical skills, attention to detail, knowledge of analytical techniques (HPLC, GC, UV-Vis etc.) and familiarity with quality control procedures. Responsible for performing routine analytical testing of raw material, in-process samples, finished products to ensure they meet quality standards and regulatory requirements. Understanding of regulatory compliance, quality management systems and document control processes, and the ability to collaborate cross-functionally and communicate effectively. Perform activities related to periodic audit trail review of all quality softwares, ensure compliance within the systems etc. Maintaining regulatory compliance in accordance with cGMP and Perform Data Integrity risk assessment of current Good Manufacturing Practices (cGMP) and GLP systems both manual and automated. Follow all safety procedures and guidelines to ensure a safe laboratory environment. Prioritize risks and work with IT, QA, laboratory personnel to mitigate data integrity gaps. Partnering with other members of the Quality Assurance team and/or end users of the system to Identify, Develop, and Implement Continuous Improvements to the Change Control System, Process, and associated procedures. Evaluate proposed and existing software systems that support laboratory and software applications for data integrity gaps. Works with IT and QA to resolve those gaps. Develop standard operating procedures for the administration of analytical and QC equipment. Ensuring the GMP status and the functionality of the laboratory equipment in accordance with the guidelines 21 CRF Part 11 on data integrity. | 08/05/2025 |
| 781 | Confluent Medical Technologies Orange County, CA Process Development Engineer I BS degree in engineering Exp: 0-3 years |
We are looking for a Process Development Engineer I to join our Laguna Niguel, CA team. As a uniquely qualified candidate, you will: Responsible for process identification, parameter optimization, proof of concept testing, technology improvements, and process implementation. Responsible for tool, extrusion, and fixture design and qualification used for manufacturing medical devices and components. Must be able to accomplish broad and complex assignments. Capable of providing technical guidance to lower level personnel. Responsible for developing processing parameters for medical devices and components. Responsible for screening and optimization of process parameters to achieve robust and stable processes and maximize yields, efficiencies and process capabilities. Plans and conducts work requiring judgment in the independent evaluation, selection, and substantial adaptation and modification of standard techniques, procedures, and criteria. Design and perform Process Characterization Study’s & DOE’s, support protocols and reports. Have a firm understanding of validation strategy (IQ/OQ/PQ), support protocols and reports. Independently performs most assignments with instructions as to the general results expected. Perform data analysis to determine product performance and capability. Responsible for generating Work Instruction, Workmanship Standards, Engineering Memos and other related documents. Understand and execute Test Methods as well as develop inspection techniques for devices or components that cannot be measured using traditional methods. Works on problems and projects of moderate scope where analysis of situation or data requires a review of identifiable factors. Selects techniques to solve complex problems and make sound design recommendations. Exercises judgment within defined procedures and practices to determine appropriate action. Demonstrates full use and application of standard principles, theories, concepts and techniques. Selects design direction or modifications of components of systems. Work with project managers to create a project plan and timeline. Receives technical guidance on unusual or complex problems and supervisory approval on proposed plans for projects. Plans, schedules, conduct, and coordinates detailed phases of engineering work in part of a major project or in a total project of moderate scope. Performs work that involves conventional engineering practice but may include a variety of complex features such as conflic | 08/05/2025 |
| 782 | Contract Pharmacal Corp Hauppauge, NY Microbiologist; Quality Control Bachelor’s degree in a science related field Exp: 1-9 years |
The Microbiologist is responsible for and has experience in performing microbial analysis for the QC Microbiology laboratory which is responsible for the analysis and disposition of commercial materials (raw materials, finished product release, stability, validation, investigation), and environmental samples, as assigned, and documenting results in accordance with SOPs. | 08/05/2025 |
| 783 | Cook Group Bloomington, IN Sterility Assurance Specialist Bachelor's degree in Engineering, Microbiology, Biology, or related field Exp: 1-2 years |
The Sterility Assurance Specialist I at Cook Incorporated is responsible for multiple projects/tasks related to ensuring continued compliance with sterilization validation and product adoption requirements. The Sterility Assurance Specialist will collaborate on cross-functional teams to perform necessary tasks relating to product/process change evaluations, sterilization validations, product adoption, and assurance of sterility requirements. | 08/05/2025 |
| 784 | Cook Group Bloomington, IN Senior Sustaining Engineer - Post Market Engineering Masters degree in Engineering or Engineering Technology or related discipline Exp: 1-2 years |
Senior Engineer, Sustaining, will perform activities related to sustaining commercially available products. These activities may include (but are not limited to) product/process remediation, risk analysis, regulatory approval support, and product/process improvements. The Senior Engineer works independently with limited supervision on complex activities and projects. The Senior Engineer acts as a mentor and leader in the department and may review/approve the work of less experienced engineers and/or contractors. | 08/05/2025 |
| 785 | CooperSurgical Houston, TX Quality Control Laboratory Technician I Bachelor’s degree in a related field Exp: 0-1 years |
The Laboratory Services Quality Technician I supports the Quality Control team by performing basic laboratory tasks, inspections, and documentation under close supervision. This entry-level role is responsible for assisting in routine quality control activities, maintaining lab cleanliness, and ensuring compliance with standard operating procedures. | 08/05/2025 |
| 786 | CooperSurgical Trumbull, CT Manufacturing Engineer I Bachelor’s degree in mechanical engineering, Industrial Engineering, or a related field Exp: 0-5 years |
The Manufacturing Engineer I at CooperSurgical is responsible for driving manufacturing excellence and optimizing production processes for our medical device and fertility products. The Manufacturing Engineer I plays a critical role in implementing lean principles, improving process efficiency, and fostering a culture of continuous improvement. | 08/05/2025 |
| 787 | Cardinal Health Mansfield, MA Post Market Vigilance Lab Support Engineer Bachelor's degree in related field Exp: 1-2 years |
CAH is currently seeking a Post market Vigilance Lab Support Engineer to join our Post market team located in Mansfield, MA (on-site). In this role, you will engage in all activities related to the CAH post market surveillance processes for returned samples. Your responsibilities will include processing returned samples and machinal testing of returned samples. | 08/05/2025 |
| 788 | Cardinal Health Mansfield, MA R&D Engineer Bachelor’s degree in mechanical engineering or a related field Exp: 0-3 years |
Under the direction of the Manager of R&D, this individual will be primarily supporting maintenance of business projects (MOB) with some potential support on New Product Development (NPD) projects. This position will have emphasis on executing against all requirements of a Design History File (DHF) including creating all product development documentation, protocols, and testing design requirements. The individual will work as a core team member supporting all aspects of the Change Development Process (CDP) as well as work with remote teams to execute on projects. This position will interact with other Research and Development groups, and Sales and Marketing, Manufacturing, Quality, Regulatory Affairs, Planning/Logistics, Packaging/Labeling and Outside Partners. | 08/05/2025 |
| 789 | Cresilon Brooklyn, NY Quality Assurance Technician B.S. in Engineering, Science, or Technology/Biotechnology Exp: 1 year |
The Quality Assurance Technician is responsible for routine inspection and testing of raw materials and components as well as of final product for Cresilon’s products in the Animal and Human Health industries. This position requires a strong attention to detail as the individual will be responsible for identifying deviations in product quality or safety and ensuring compliance with local, state, and federal regulations, including current Good Manufacturing Practices (cGMP). Position is for 2nd shift. | 08/05/2025 |
| 790 | Crown Bioscience San Diego, CA Research Associate I, In vivo Bachelor's degree Exp: 6 months |
The purpose of the In Vivo Research Associate I position is to provide support on In vivo studies within the In Vivo Pharmacology group meeting Company's goals, objectives and quality standards. | 08/05/2025 |
| 791 | CSL Chattanooga, TN Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 08/05/2025 |
| 792 | CSL Houston, TX Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 08/05/2025 |
| 793 | CSL Milwaukee, WI Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 08/05/2025 |
| 794 | Curia Rensselaer, NY Quality Investigations Specialist II MA/MS Degree in Biology or Chemistry or a a relevant field Exp: 1 year |
The Quality Investigation Specialist II plans and conducts activities concerned with the quality assurance of industrial processes, materials, and products. The role is responsible for overseeing and providing support for GMP investigations, internal audits, and customer complaint investigations. This role serves the Quality Assurance Department by implementing all procedures leading to compliant, valid, and documented release of drug, biologic product, or medical device by performing the following duties personally or through subordinate specialists. The Quality Assurance Specialist II participates in, writes and/or closes investigations. This requires maintaining budgetary targets and delivering earnings and growth to the company. | 08/05/2025 |
| 795 | Curia Albuquerque, NM Microbiologist I Bachelor’s degree in a scientific discipline, preferably microbiology or related field Exp: 1 year |
The Microbiologist I is responsible for performing microbiological testing and quality activities to support product production, environmental monitoring, and product release in a pharmaceutical manufacturing environment. This role ensures compliance with regulatory requirements and company standards by conducting microbiological assays, analyzing trends, and accurately documenting and reporting results. The QC Microbiologist I collaborates with cross-functional teams to identify potential microbiological risks, troubleshoot deviations, and contribute to continuous improvement initiatives to maintain product quality and patient safety. | 08/05/2025 |
| 796 | Curia Albuquerque, NM QC Analyst I Bachelor’s degree in Chemistry or related field Exp: 0-3 years |
The Quality Control Analyst I is responsible for performing routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished APIs, and stability samples. This role also participates in special projects, method development/transfers and cleaning study qualifications. | 08/05/2025 |
| 797 | Curia Rensselaer, NY QC Analyst I Bachelor’s degree in Chemistry or related field Exp: 0-3 years |
The Quality Control Analyst I is responsible for performing routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished APIs, and stability samples. This role also participates in special projects, method development/transfers and cleaning study qualifications. | 08/05/2025 |
| 798 | Curium Maryland Heights, MO Quality Control Technician Bachelor Degree in life science or a related field Exp: 1+ years |
Perform assigned laboratory testing and related quality control activities in order to ensure compliance with applicable SOP's and cGMPs. Provide timely testing and notification of any aberrant occurrence to Management/Supervision that presents potential negative impact to manufactured or marketed product. | 08/05/2025 |
| 799 | Davita Deland, FL Assistant II, Laboratory Bachelor’s Degree Biological Sciences Exp: 0-2 years |
The Assistant II, Lab performs specimen accessioning, data entry, processing and other non-technical duties in the laboratory under the general supervision of the Supervisor. This position reports to Supervisor or Manager of Chemistry. This position does not require a registry license and may be non-technical; may be assigned to work a designated shift on day/evening/night. This position reports to the Manager, Laboratory (Lab). | 08/05/2025 |
| 800 | Dexcom San Diego, CA QA Engineer 2 Masters degree in a technical discipline Exp: 0-2 years |
This functional department provides technical support and guidance to product teams to ensure conformance to product development process and other applicable safety and quality system regulation and standards (e.g. IEC 62304, ISO 13485, ISO 14971). We are responsible for various aspects of Design Assurance with focus on product improvement, new product development and defect prevention. We interface with different cross functional groups (Product HW/SW Engineering, Software Test, Regulatory Affairs, Marketing, Project managers, Systems Engineering and others). We work closely with cross functional teams to establish and ensure compliance and quality for product related risk management documentation. Perform risk assessments and evaluations for products that conform to established standards and agency regulations. | 08/05/2025 |
| 801 | Dexcom San Diego, CA R&D Mechanical Engineer Masters degree in a technical discipline Exp: 0-2 years |
As an R&D Mechanical Engineer 2, you will be in a high visibility, high impact role both driving the design, development and implementation of new products, as well as providing ongoing support for existing on-market products. You will lead cross-functional discussions as the R&D Mechanical Engineering representative to ensure product quality, reliability, and performance while proactively driving continuous improvement efforts. | 08/05/2025 |
| 802 | Diacarta Pleasanton, CA Clinical Laboratory Assistant BS/BA in life science Exp: 0-1 years |
A CLA performs laboratory duties under the supervision of a licensed CLS. This position is for assisting the CLS and for sample processing, equipment operation and maintenance, and documents. | 08/05/2025 |
| 803 | Diacarta Pleasanton, CA Research Associate I, In vivo BS or MS degree in molecular biology or a related field Exp: 0-2 years |
DiaCarta is seeking a highly motivated, independent, and interactive Research Associate to join the R&D function in the company. The new team member will participate in R&D activities with the goal of developing and launching new qPCR, NGS, and branched DNA tests for IVD cancer diagnostics applications. The successful candidate will have outstanding attention to detail, enjoy working in a fast-paced multidisciplinary team environment, and have exceptional hands-on laboratory skills. DiaCarta is a rapidly growing company, so the candidate must be highly motivated and committed to launching their career in an innovative area of molecular diagnostics. This is a full-time role in Richmond, and you will be reporting to the Senior Scientist. | 08/05/2025 |
| 804 | Diacarta Pleasanton, CA Manufacturing Technician B.S. degree in Molecular Biology, Cell Biology, Biotechnology or related field Exp: 1 year |
This position is a member of a fast-paced production team and will be responsible for the following tasks. Purchase raw materials from a vendor. Receive incoming materials and perform inspection and inventory recording. Production of DiaCarta IVD products to meet sales demands. Labeling of raw materials and finished goods. Perform calibration or preventative maintenance of the instrument. Participate in process improvement projects. Compliance with corporate quality systems. Other on-the-job assignments indicated by management. | 08/05/2025 |
| 805 | Bristol Myers Squibb Indianapolis, IN Associate Scientist I, Microbiology Bachelor’s degree in biology, Microbiology, or other Life Science related field Exp: 0-1 YEARS |
RayzeBio, a Bristol Myers Squibb company, is seeking applicants for an Associate Scientist, I for the Microbiology department. Reporting to the Manager of Microbiology, this role will help support the contamination control and sterility assurance testing activities at the manufacturing facility in Indianapolis. This role will conduct environmental monitoring and microbiological release testing of aseptically produced targeted alpha therapy (TAT) radiopharmaceuticals for RayzeBio’s clinical and commercial programs. | 07/30/2025 |
| 806 | Bristol Myers Squibb Summit West, NJ Manufacturing Associate, CAR T Media and Solution Preparation Bachelor’s degree Exp: No exp |
Our Manufacturing Associate, Cell Therapy team manufactures human blood derived components per Batch Record and Standard Operating Procedures in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Job duties are performed within a team according to an assigned, production shift schedule. Communication of production deviations and assistance with quality investigations are required, as applicable. | 07/30/2025 |
| 807 | Bristol Myers Squibb Devens, MA Associate, QC Analytical, Cell Therapy Bachelor's degree preferred in science Exp: 0-2+ years |
The Associate, QC Analytical, Cell Therapy is responsible for supporting QC testing for in-process, final product, and stability samples. May assist with documentation, deviations, investigations, and continuous improvement efforts. | 07/30/2025 |
| 808 | Bristol Myers Squibb Summit West, NJ Manufacturing Associate, Cell Therapy Bachelor’s degree Exp: No exp |
Our Manufacturing Associate, Cell Therapy team manufactures human blood derived components per Batch Record and Standard Operating Procedures in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Job duties are performed within a team according to an assigned, production shift schedule. Communication of production deviations and assistance with quality investigations are required, as applicable. | 07/30/2025 |
| 809 | Bristol Myers Squibb Indianapolis, IN Associate Scientist II, Isotope Production Bachelors degree in Chemistry or related science Exp: 1-3 years |
Reporting to the Supervisor of Quality Control, the associate scientist will help support the establishment of a new Quality Control laboratory which supports RayzeBio’s Isotope Production process in Indianapolis. The associate scientist will be providing support for the qualification and validation of analytical and radiochemical equipment for the QC lab. This position will conduct inspections and testing of raw materials, in-process controls, and finished products, ensuring compliance with specifications and regulatory standards. Specifically, the associate scientist will support the manufacture release of isolated isotopes to support RayzeBio’s clinical programs. | 07/30/2025 |
| 810 | Bristol Myers Squibb Devens, MA Manufacturing Associate, Cell Therapy Bachelors in relevant science or engineering Exp: 0-2 years |
The Manufacturing Associate, Cell Therapy brings enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs. The incumbent must be goal-oriented, flexible, and able to work efficiently with safety and quality in mind, with a good understanding of good manufacturing practices to support routine manufacturing operations for Cell Therapy. | 07/30/2025 |
| 811 | Bristol Myers Squibb Indianapolis, IN Sr. Associate Scientist I MS in chemistry or related field Exp: 1-5 years |
RayzeBio is seeking a Senior Quality Control Chemist I reporting to the Quality Control Supervisor. The position will be responsible to ensure the testing and analysis of RayzeBio’s radiopharamceuticals are analyzed to cGMP standards. The applicant will be also be responsible to mentor junior chemists, provide technical support and liaise to other functional units, and to maintain an appropriate laboratory safety culture. The position will be located at RayzeBio’s manufacturing plant, in Indianapolis, IN. | 07/30/2025 |
| 812 | BWXT Erwin, TN Quality Engineer 1 B.S. Degree Exp: 1 year |
Assist senior Quality Engineers to develop, implement, and audit Quality Assurance and Quality Control systems to assure compliance to customer requirements or national standards. Assist senior Quality Engineer(s) to maintain the quality of specific products. Assist in the performance of system evaluations to assure compliance with customer, regulatory, or internal specifications. Continually strive for improved quality standards that shall lower costs of products and processes at NFS. | 07/30/2025 |
| 813 | BWXT Erwin, TN AUKUS Engineer 2 M.S. Degree in Engineering Exp: 1 year |
Evaluates situations, selects and applies standard engineering techniques, procedures and criteria, using judgment in making minor modifications. Assignments have a clear objective and require planning and investigation of limited number of possibilities. Work is reviewed for application of sound judgement and compliance with contract technical requirements and meeting of Division policies and procedures. Receives instructions on specific assignment objectives, complex features and possible solutions. Assistance is furnished on unusual problems and work is reviewed for application of sound professional judgment. | 07/30/2025 |
| 814 | BWXT Erwin, TN Engineer 1 - Electrical & Instrumentation Eng Bachelor’s degree in Engineering Exp: No exp |
Responsible for routine engineering assignments applying standard engineering techniques, procedures, and criteria under guidance of a manager or experienced engineer. Assignments are designed to develop professional work knowledge and abilities. Works under close supervision. Manager screens assignments for unusual or difficult problems and selects techniques and procedures to be applied on non-routine work. | 07/30/2025 |
| 815 | BWXT Erwin, TN Engineer 1 - Engineering (PIPELINE) Bachelor’s degree in Engineering Exp: No exp |
Responsible for routine engineering assignments applying standard engineering techniques, procedures, and criteria under guidance of a manager or experienced engineer. Assignments are designed to develop professional work knowledge and abilities. Works under close supervision. Manager screens assignments for unusual or difficult problems and selects techniques and procedures to be applied on non-routine work. | 07/30/2025 |
| 816 | BWXT Erwin, TN Engineer 2 - Fuel Process Engineering M.S. Degree in Engineering Exp: 1 year |
Evaluates situations, selects and applies standard engineering techniques, procedures and criteria, using judgment in making minor modifications. Assignments have a clear objective and require planning and investigation of limited number of possibilities. Work is reviewed for application of sound judgement and compliance with contract technical requirements and meeting of Division policies and procedures. Receives instructions on specific assignment objectives, complex features and possible solutions. Assistance is furnished on unusual problems and work is reviewed for application of sound professional judgment. | 07/30/2025 |
| 817 | BWXT Erwin, TN Engineer 2- Fuel Dev & Variability Reduction M.S. Degree in Engineering Exp: 1 year |
Evaluates situations, selects and applies standard engineering techniques, procedures and criteria, using judgment in making minor modifications. Assignments have a clear objective and require planning and investigation of limited number of possibilities. Work is reviewed for application of sound judgement and compliance with contract technical requirements and meeting of Division policies and procedures. Receives instructions on specific assignment objectives, complex features and possible solutions. Assistance is furnished on unusual problems and work is reviewed for application of sound professional judgment. | 07/30/2025 |
| 818 | BWXT Erwin, TN Engineer 2 -- Design Engineering -- Mechanical M.S. Degree in Engineering Exp: 1 year |
Evaluates situations, selects and applies standard engineering techniques, procedures and criteria, using judgment in making minor modifications. Assignments have a clear objective and require planning and investigation of limited number of possibilities. Work is reviewed for application of sound judgement and compliance with contract technical requirements and meeting of Division policies and procedures. Receives instructions on specific assignment objectives, complex features and possible solutions. Assistance is furnished on unusual problems and work is reviewed for application of sound professional judgment. | 07/30/2025 |
| 819 | Cambrex Charles City, IA Project Engineer BS in Engineering or equivalent degree Exp: 1-3 years |
The Project Engineer performs general engineering duties for new installations and equipment, and modification of existing facilities and equipment. These duties are to be carried out with safety, efficiency and quality at the forefront. | 07/30/2025 |
| 820 | Cambrex Charles City, IA Process Engineer BS in Chemical Engineering Exp: 1-3 years |
The Process Engineer will be responsible for implementation of projects for the manufacture of APIs and bulk intermediates and other products from development through piloting and/or commercial production. | 07/30/2025 |
| 821 | Cambrex Waltham, MA Chemical Process Technician Bachelor’s Degree in Chemical Process Technology, Chemistry, or Chemical Engineering Exp: 1 year |
We are looking for candidates who have a passion for working in a fast-paced, dynamic environment. The ideal candidate will have an Associate’s or Bachelor’s Degree in Chemical Process Technology, Chemistry, Chemical Engineering, or equivalent with one or more years of relevant experience, or a High School or GED degree with 10 years experience. The candidate should enjoy working in the field with their hands. The candidate should be well versed in handling equipment related to chemical processing, including working with glassware, compression fittings, tubing, pumps, and laboratory operations such as following chemical process recipes. From time to time, the candidate will also support general facility operations, including cleaning, waste management, and organization of various areas of the facility. | 07/30/2025 |
| 822 | Cambrex Longmont, CO Associate Scientist, Manufacturing BS in chemistry or related field Exp: 0-3+ years |
The Associate Scientist, Manufacturing will work within a team to perform kilogram scale organic synthesis of pharmaceutical drug substance. The Associate Scientist will operate chemical manufacturing equipment and execute detailed written instructions from a batch record under Good Manufacturing Practice (cGMP) conditions. In addition, the Associate Scientist is responsible for maintaining the manufacturing suites for activities by properly setting up, breaking down, operating, and cleaning production equipment for both GMP and non-GMP drug substance manufacturing operations. An Associate Scientist in manufacturing will operate under and develop subject matter expertise in cGMP practices and Good Documentation practices (GDP) within the Quality Management System. | 07/30/2025 |
| 823 | Cambridge Isotope Laboratories Andover, MA Quality Control Analyst II (LC/MS) Master's degree in Chemistry or a related field Exp: 1-2 years |
The Quality Control (QC) Analyst II is responsible for conducting routine and non-routine analysis of GMP and ISO materials under general supervision and in accordance with standard operating procedures (SOPs). They compile data for documentation of test procedures and prepare reports. They also calibrate and maintain lab equipment. They are able to perform basic troubleshooting and maintenance independently. Occasional travel between sites may be required. | 07/30/2025 |
| 824 | Cambridge Isotope Laboratories Twewksbury, MA Analytical Chemist MS in Chemistry, or other relevant science degree Exp: 1+ years |
The Analytical Chemist (GMP/RP/ISO) is responsible for providing laboratory support by researching and developing methods and implementing new analytical techniques, to be used for batch release testing of existing and new products. This may include performing validations or verifications of methods to ensure they are suitable for use. They are also responsible for providing support for investigations of out of specification or out of trend results and troubleshooting other analytical issues. They compile data for trending, assessment, and presentation of results and prepare reports under GMP guidelines and Standard Operating Procedures (SOP’s). They will also perform analytical work including maintaining laboratory instruments and equipment. | 07/30/2025 |
| 825 | Candel Needham, MA Contract Research Associate – Virology MS in Virology, Biotechnology, or related field Exp: 1-3 years |
We are seeking a highly motivated and collaborative Research Associate with a strong foundation in virology to support the development of next-generation HSV-1 viral immunotherapy candidates. This individual will contribute to the enLIGHTEN™ Discovery Platform through hands-on experimental work, including viral vector testing, mammalian cell culture, and virology-specific assays. The ideal candidate will bring a passion for innovation and a desire to work in a fast-paced, cross-functional research environment. | 07/30/2025 |
| 826 | Caris Phoenix, AZ Clinical Engineering Technician Bachelor's or Master’s degree in a science field Exp: 1 year |
The Clinical Engineering Technician is responsible for the installation and maintenance of equipment within the clinical molecular lab. | 07/30/2025 |
| 827 | Carlsbad Technology San Diego, CA Quality Control Chemist BS or Master Degree in organic chemistry, physical organic chemistry or Life Sciences Exp: Entry Level |
This position is responsible for the operation of laboratory equipment and will perform tests independently once training has been completed. The successful Chemist will be able to establish a congenial relationship with other employees to maintain a pleasant work environment and must have strong organizational skills and time management skills. | 07/30/2025 |
| 828 | Caris Phoenix, AZ Molecular Technologist, Solid Tumor Bachelor’s degree in scientific field Exp: 1 year |
The Molecular Technologist – Solid Tumor is responsible for performing various high complexity molecular techniques that include but are not limited to nucleic acid extractions and next generation sequencing (NGS). This position works under the direction of the supervisor and follows standard laboratory procedures and policies. | 07/30/2025 |
| 829 | Castle Biosciences Inc. Phoenix, AZ Lab, Molecular Technologist (Derm) B.S. in a scientific discipline Exp: 1-2 years |
A typical day for a molecular technologist involves extracting and analyzing RNA samples using various molecular laboratory techniques. This includes RNA quantification, PCR, reagent quality control, and instrument maintenance, all while interpreting data to ensure the accuracy and reliability of results. The role requires proficiency in molecular techniques, maintaining optimal working conditions, and upholding stringent quality control measures. Collaborating with team members is also integral to supporting an efficient workflow and maintaining high standards within the laboratory. | 07/30/2025 |
| 830 | Catalent Kansas City, MO Analytics Associate Scientist II Bachelor's degree in related scientific field Exp: No exp |
Catalent Pharma Solutions in Kansas City, MO is hiring an Analytics Associate Scientist II. Under general supervision, the Associate Scientist II performs work that is varied in analytical development and that may be somewhat difficult in character. Some evaluation, originality or ingenuity is required at the Associate Scientist II level. This individual follows established protocols and work plans and may be assisted by laboratory technicians/assistants. | 07/30/2025 |
| 831 | Catalent Baltimore, MD Associate Scientist III, - Downstream M.S. Degree in Engineering or Life Science Exp: 1+ years |
The Process Development Department is responsible for upstream and downstream process development, pilot scale execution, and tech transfer of developed processes to GMP manufacturing. This individual performs collaboratively and productively as an Associate Scientist III Downstream Development and actively engages in process development within a dynamic project team. Displays strong technical knowledge, initiative, and scientific commitment and makes significant technical contributions within the Process Development Group. Maintains openness to understanding areas outside of the primary function in order to foster continuous improvement. | 07/30/2025 |
| 832 | Catalent Kansas City, MO Associate, Quality Assurance Bachelor’s degree in a scientific field Exp: No exp |
The Associate, Quality Assurance (QA) is responsible for quality oversight of manufacturing “floor” activities and the associated in-process GMP (Good Manufacturing Practices) records. In addition to day-to-day responsibilities, the QA Associate will identify and participate in opportunities to improve processes. | 07/30/2025 |
| 833 | Catalent Kansas City, MO Quality Control Associate Scientist II Bachelor's degree in related life science or physical science field required (Biology or Microbiology preferred) Exp: No exp |
The Catalent site in Kansas City, MO is hiring a Quality Control (QC) Associate Scientist II. The QC Associate Scientist II performs tasks from detailed instructions and established procedures. This person will learn and comply with site Standard Operating Procedures (SOPs), corporate policies, and Environmental Health and Safety requirements. You will use basic knowledge of the principles and concepts of Biology & Chemistry for testing purposes. We’re seeking a self-motivated, detail-oriented person who is able to make decisions and solve problems independently or in a team environment. | 07/30/2025 |
| 834 | Catalent Chelsea, MA Manufacturing Associate Bachelor’s Degree in Life Sciences or Engineering Exp: 1 year |
Catalent Pharma Solutions is hiring a Manufacturing Associate performs routine and complex operations for the GMP production of pharmaceutical products. This individual operates in accordance with environmental, health, safety, and cGMP guidelines. This individual is responsible for the hands-on execution of production activities as they relate to spray drying operations of manufactured products. | 07/30/2025 |
| 835 | Catalent Greenville, NC Sample Management Specialist I BA or BS degree in science Exp: No exp |
The Sample Management Specialist I performs various activities within Quality Control with primary focus on sample management from external customers or internal departments centered around stability, reference standards, DEA control substances and sample logistics. The Sample Management Specialist I follows all regulatory guidelines, cGMP guidelines, Environmental Health and Safety regulations as required by the job function. | 07/30/2025 |
| 836 | Catalent Morrisville, NC Quality Control Chemist II Master’s degree in scientific or engineering field Exp: 1+ years |
Catalent Pharma Solutions is Morrisville, NC is hiring a Quality Control Chemist II. The Quality Control Chemist II will independently perform work using a variety of methodology. Experience in a variety of analytical techniques and instrumentation is required. These may include compendial testing, identification techniques (i.e. FTIR), chromatography, among others. The Quality Control Chemist II will perform scientific analysis of data and draw reasonable conclusions, follow established methods and protocols, perform initial troubleshooting and investigations as needed, demonstrate leadership skills regarding guiding and training less experienced colleagues and comply with the company safety and operational requirements and procedures requirements. | 07/30/2025 |
| 837 | Celerion Lincoln, NE Scientist/ Associate Scientist of Laboratory Automation Bachelor's degree in science or engineering-related field Exp: 1 year |
Celerion is hiring a Scientist/ Associate Scientist of Laboratory Automation to join our Lincoln, NE Bioanalytical team. This role will work onsite daily with our Hamilton, Tecan and Sciclone instruments. In this role, you will perform research and/or development in collaboration with scientific teams and automated systems based on new and existing methodologies. This hands-on role focuses on programming and operating laboratory automation systems with the objective of becoming the subject matter expert for all laboratory automation technologies within our organization. | 07/30/2025 |
| 838 | Cellares Bridgewater, NJ Process Engineer (I, II, III) Bachelor’s or Master’s degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering, or a related field Exp: 0-4 years |
We are seeking an innovative and highly motivated Process Engineer on our MSAT team who will contribute significantly to establishing our IDMO Smart Factories. This position is focused on supporting the development and implementation of automated cell therapy manufacturing processes. You will work closely with the Process Engineering Lead and other cross-functional teams to execute, develop, design, optimize, and validate processes to ensure efficient, high-quality, scalable manufacturing solutions. This is a multidisciplinary role & this individual will interface across many parts of the company (with customers, scientists, researchers, and engineers) to develop the best solutions possible. Candidates should enjoy working in a fast-paced, mission-driven environment and be prepared to tackle a broad selection of challenges as the company grows. | 07/30/2025 |
| 839 | Cellares South SF, CA Cell Therapy Manufacturing Specialist Bachelor’s Degree or diploma in a scientific or related field Exp: 1+ years |
We are seeking an innovative and highly motivated Cell Therapy Manufacturing Associate to join our Process Sciences team who will contribute significantly to the development and manufacture of our advanced cell therapy manufacturing platform. The primary focus of this position will be to support manufacturing operations, as well as day-to-day lab operations. This is a hands-on position that will train in Process Development, Analytical Development, and/or MSAT prior to joining the Manufacturing Group. | 07/30/2025 |
| 840 | Cellipont Bioservices Woodlands, TX EM Technician, I Bachelor's degree in Microbiology, Biology, or related field Exp: 0-1 years |
Cellipont Bioservices is growing, and we are looking for a EM Technician I, who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The EM Technician I is responsible for Environmental Monitoring sampling, analyzing, and reporting results, to support manufacturing. Works in a fast-paced environment supporting the quality control department of a CMDO for manufacturing of biologic bulk drug substance, sterile finished drug product, and fill/finish. | 07/30/2025 |
| 841 | Cellipont Bioservices Woodlands, TX Manufacturing I Bachelors Degree in Life Sciences Exp: 0-1+ years |
Cellipont Bioservices is growing, and we are looking for a Manufacturing Associate I who believe in the potential bridging client's discoveries to patient cures and who want to challenge the status quo and take Cellipont and its clients to the next level. The Manufacturing Associate I is an entry level role and will be responsible for assisting in the planning and timely execution of manufacturing operations for a cGMP-compliant state-of-the-art cell processing/clinical manufacturing facility with emphasis on primary cell isolation and cell culture in an aseptic processing environment. The Manufacturing Associate I is responsible for following the standard practices outlined for the operation of the facility in accordance with the regulatory requirements for the manufacture of materials for our clinical studies, clinical trials and products. | 07/30/2025 |
| 842 | Cellipont Bioservices Woodlands, TX QA Technician I, Operations Bachelor's Degree Exp: 0-1 years |
Cellipont Bioservices is growing, and we are looking for a QA Technician I, Operations who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The QA Technician I, Operations will be responsible for monitoring systems and procedures to ensure compliance where applicable. The QA Technician I, Operations is responsible for providing Quality Assurance support real-time for GMP Manufacturing of Cell Therapies. This individual will be responsible for providing QA on the Floor during manufacturing including observing critical processes, review executed GMP documentation, and supporting other QA functions as needed. | 07/30/2025 |
| 843 | Cellipont Bioservices Woodlands, TX QA Technician II, Operations Bachelor's Degree Exp: 1-2 years |
Cellipont Bioservices is growing, and we are looking for a QA Technician II, Operations who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The QA Technician II, Operations will be responsible for monitoring systems and procedures to ensure compliance where applicable. The QA Technician II, Operations is responsible to provide Quality Assurance support real-time for GMP Manufacturing of master/working cell banks. This individual will be responsible for providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. | 07/30/2025 |
| 844 | Cellipont Bioservices Woodlands, TX QC Analyst I, Analytical Bachelors Degree preferred in Life Sciences discipline Exp: 0-1 years |
Cellipont Bioservices is growing, and we are looking for a QC Analyst I, Analytical who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The QC Analyst I, Analytical will work in a fast-paced environment supporting the quality control department of a CDMO for manufacturing of cell therapies. The QC Analyst I, Analytical will be responsible for routine testing, assay transfer and assay validation, QC document preparation and revision (SOPs/Protocols/Reports), as well as support for laboratory setup and maintenance. The QC Analyst I, Analytical, will also be responsible for ensuring all activities are executed timely and cost effectively to ensure customer and stakeholder satisfaction. This role will also require the individual to demonstrate a strong ability to work cross-functionally and possess strong leadership skills. | 07/30/2025 |
| 845 | Bausch + Lomb Tampa, FL Microbiology Technician III Bachelor’s degree in microbiology, Biology, or equivalent Life Science Exp: 1-2 years |
Perform routine and non-routine microbiological testing and environmental monitoring (EM) in support of sterile manufacturing operations. | 07/24/2025 |
| 846 | Bayer Ankeny, IA Research and Development Specialist II Bachelor’s or master’s degree in biology, Chemistry, Engineering, or other life science fields Exp: 1 year |
This Production Genotyping position (Research and Development Specialist II – 2nd Shift: Monday through Thursday, 3:00 pm to 2:00 am) is responsible for collaborating with laboratory team members to ensure timely delivery of high-quality data. The role requires achieving and surpassing daily and weekly production Key Performance Indicator targets, ensuring strict adherence to safety and compliance policies, identifying and executing experiments that drive process and system improvements, as well as operating and maintaining automation equipment. | 07/24/2025 |
| 847 | Beckman Coulter Diagnostics Miami, FL Manufacturing/Process Engineer II Master’s degree in Engineering in mechanical, electrical, and industrial Exp: 0+ years |
The Manufacturing/Process Engineer II for Beckman Coulter Diagnostics is responsible for providing day to day technical support and driving complex root cause investigations, for the instrument manufacturing product lines, including the assembly and final test processes, to drive quality and on-time delivery for our customers. This position is part of the Manufacturing Operation located in Miami, Florida and will be on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Manufacturing Engineering Team and report to the Manufacturing Engineering Manager responsible for providing technical support to the manufacturing lines of Beckman Coulter’s premier Diagnostics products. If you thrive in a challenging, cross-functional, and fast-paced role and want to work to help build a world-class manufacturing organization—read on. | 07/24/2025 |
| 848 | Beckman Coulter Diagnostics Chaska, MN Manufacturing Engineer II Master’s degree in engineering field Exp: 0-2 years |
The Manufacturing Engineer II at Beckman Coulter Diagnostics is responsible for providing support and solving problems in the manufacturing process, from assembly to final packaging, across multiple instrument value streams. This role emphasizes driving continuous improvement initiatives to enhance efficiency, quality, and productivity. Additionally, the Manufacturing Engineer II will be accountable for leading efforts in design transfer efforts to meet business objectives. You will work cross-functionally to drive business results, DBS culture, and executing on strategic plans to achieve long term objectives. This position is part of the Hardware Operations located in Chaska, MN and will be an on-site position. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Manufacturing Technical Operations Team and report to the Engineering Manager responsible for Hardware Manufacturing. If you thrive in a fast paced, high visibility role and want to work to build a world-class manufacturing organization—read on. | 07/24/2025 |
| 849 | Beckman Coulter Diagnostics Chaska, MN Development Scientist I Bachelor's Degree in Life Science (Chemistry, Biology, Microbiology Biology or related science) Exp: 0+ years |
The Development Scientist I is responsible for responsible for participating in development and commercialization of immunoassays for an automated system. This person will assist in executing and analyzing experimental data as well as provide and presenting conclusions with team members as needed. They will participate in characterization, verification and validation of new and modified product designs. Additionally, you will be responsible for documentation of studies performed, including materials, methods, and conclusions. | 07/24/2025 |
| 850 | BD Franklin Lakes, NJ R&D Engineer II Bachelors Degree in Mechanical Engineering Exp: 1-5+ years |
The R&D Engineer II will be a key contributor on a R&D team within Medication Delivery Solutions, Injection Systems. The individual in this position will have understanding and exposure to a wide application of technical principles, theories and concepts. The R&D Engineer II provides solutions that are imaginative, thorough and practical to a wide range of complex problems. | 07/24/2025 |
| 851 | Bifrost Berkeley, CA Mechanical Engineer BS or MS in Mechanical Engineering or a related field Exp: 0-4 years |
Are you passionate about pushing the limits of technology to advance our understanding of the life sciences? So are we! We’re looking for a highly motivated and experienced Mechanical Engineer to join a fast-paced start-up developing tools that will transform functional cell biology research. The ideal candidate will have strong engineering and problem-solving skills, a solid grasp of mechanical design fundamentals and some exposure to optical systems, microscopy and bio-engineering or biology. As Mechanical Engineer, you will be part of a small team designing, developing, specifying and testing Bifrost’s hardware products. Additionally, you will play a role in product definition, development and verification testing. | 07/24/2025 |
| 852 | BioMérieux Salt Lake City, UT Manufacturing Engineer II Master’s degree in engineering or related discipline Exp: 1-3 years |
This engineer works on a cross-functional Manufacturing Engineering team to support several aspects of the consumable manufacturing process. Partners with internal team members and vendors to optimize product performance. Performs troubleshooting and routine maintenance of basic to moderate manual and automated manufacturing processes. Leverages experience and skillset to implement best practices within the realm of consumable medical device manufacturing by identifying root causes and recommending solutions. Contributes to the resolution of basic to moderate manufacturing engineering problems. | 07/24/2025 |
| 853 | BioMérieux Salt Lake City, UT Reagent Technical Project Manager III Bachelor’s degree in life sciences or Engineering Exp: 2 years |
The Technical Project Manager is assigned to projects within Reagent Manufacturing. This individual will collaborate with various leaders within manufacturing including operations, engineering, continuous improvement and other subject matter experts to create project documentation and implement projects on schedule as well as within accordance with design control and QMS requirements. In addition to meeting regularly with assigned project resources, this individual is also expected to provide regular project updates to leaders and stakeholders within the organization. | 07/24/2025 |
| 854 | BioMérieux Durham, NC QC Analyst 2-Night Shift Master's Degree in Biology, Chemistry or Biochemistry Exp: 0 years |
This position is in a fast-paced, FDA regulated environment in the Medical Devices/Diagnostics Industry. The QC Biochemistry Analyst 2 will be in a key position in the Biochemistry laboratory performing testing of Description, pH, FTIR, Osmolality, Moisture Analysis, Solubility, Loss on Drying, Resin Ratio, Reflectance, and pO2 Headspace Analysis, HPLC. | 07/24/2025 |
| 855 | BioMérieux Salt Lake City, UT Production Coordinator I (C Shift, Nights) Bachelor’s degree in a Biology/Chemistry or Supply Chain Exp: 1 year |
The Production Coordinator organizes and prepares work within a manufacturing group. Follows a production schedule to coordinate and organize resources necessary for production work orders and to ensure production flows smoothly and efficiently. Creates production batch records, prints/prepares labels, and gathers assigned materials lots for production orders. Participates in cycle counts, delivery of QC samples, and delivery/transaction of R&D materials. Ensures comprehensive compliance for proper documentation of batch records and material requirements for the production staff. Interfaces between production departments and with production schedulers, materials management, QA, and R&D to properly prepare the production orders per schedule requirements. Communicates any potential scheduling issues to the affected groups, and works with the production schedulers and scheduling manager to resolve scheduling issues. Monitors inventory status of production sub-assemblies critical to the manufacturing process, and communicates potential shortages to the production scheduler. Collects, reviews, and inputs data into databases. Normally receives general instruction on routine work and detailed instruction on new assignments. The Production Coordinator may participate in process improvements and other documentation efforts. | 07/24/2025 |
| 856 | BioMérieux Salt Lake City, UT Production Coordinator I (A Shift) Bachelor’s degree in a Biology/Chemistry or Supply Chain Exp: 1 year |
The Production Coordinator organizes and prepares work within a manufacturing group. Follows a production schedule to coordinate and organize resources necessary for production work orders and to ensure production flows smoothly and efficiently. Creates production batch records, prints/prepares labels, and gathers assigned materials lots for production orders. Participates in cycle counts, delivery of QC samples, and delivery/transaction of R&D materials. Ensures comprehensive compliance for proper documentation of batch records and material requirements for the production staff. Interfaces between production departments and with production schedulers, materials management, QA, and R&D to properly prepare the production orders per schedule requirements. Communicates any potential scheduling issues to the affected groups, and works with the production schedulers and scheduling manager to resolve scheduling issues. Monitors inventory status of production sub-assemblies critical to the manufacturing process, and communicates potential shortages to the production scheduler. Collects, reviews, and inputs data into databases. Normally receives general instruction on routine work and detailed instruction on new assignments. The Production Coordinator may participate in process improvements and other documentation efforts. | 07/24/2025 |
| 857 | BioMérieux Salt Lake City, UT BioReagents Formulator (C Shift) Bachelor’s degree with an emphasis on a biological science Exp: 1+ years |
Responsible for manufacturing products efficiently, accurately, safely and on time. Operates manufacturing equipment and in-process instrumentation to manufacture regulated products in accordance to QSRs, company policy and safety regulations. Works on assignments that are routine in nature where ability to recognize deviation from accepted practice is required. Position requires attention to detail and fine motor dexterity. Relies on instructions and pre-established guidelines to perform the functions of the job and requires direct supervision or oversight by a senior employee. Works under immediate supervision of the BFDX Formulation Team Lead and reports to the BFDX Reagent Production Supervisor. | 07/24/2025 |
| 858 | Biogen Research Triangle Park, NC Manufacturing Associate III Bachelor’s Degree (STEM preferred) Exp: 6 months |
Our Manufacturing Associates perform processing steps and manufacturing support activities in our facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in;MAs perform these critical steps in a clean environment governed by Current Good Manufacturing Practices (cGMP). | 07/24/2025 |
| 859 | Biogen Research Triangle Park, NC Engineer II, Automation B. S. in Engineering in Automation, Electrical, Chemical, Mechanical Engineering, or a similar Engineering discipline Exp: 0-2 years |
As part of our Automation & MES team, the Engineer II, Automation plays a pivotal role in supporting Biogen's RTP Bio site's operational and project goals. This position primarily focuses on maintaining and troubleshooting process control system hardware and software, including DeltaV DCS and Syncade MES, for biopharmaceutical manufacturing. You'll be responsible for creating software design specifications, implementing new control strategies, authoring recipes, and developing software test protocols for new products and processes. Additionally, you'll perform Responsible Engineering duties, such as reviewing validation protocols and creating Change Controls for system modifications. This role requires participation in an on-call rotation for troubleshooting and manufacturing support, managing small to medium engineering projects, and collaborating with cross-functional teams to drive improvements. Your work will directly contribute to optimizing our manufacturing operations and ensuring seamless production processes. | 07/24/2025 |
| 860 | BioLegend San Diego, CA Research Associate II - Cell Analysis Bachelor’s Degree in life sciences or Engineering Exp: 6+ months |
At BioLegend (a Revvity, Inc. company) we develop novel, cutting edge products and offer custom services to help with scientific innovation and discovery. We are currently looking for a talented, detail oriented person to join our growing Product Development team. The potential candidate will assist with development of new products for cell analysis such as antibodies, multi-color panels, and reagents for analysis of cell metabolism and cell imaging. The successful candidate must be a self-motivated, team player, able to communicate effectively with a multi-disciplinary team and must possess excellent organization skills. | 07/24/2025 |
| 861 | BioLegend San Diego, CA Biochemist I – GMP Bachelor’s degree Exp: 1 year |
The Biochemist I – GMP position will be responsible for the different stages of manufacturing various BioLegend’s regulated product produced in our US FDA registered cGMP manufacturing facility. This role will be responsible for formulating and vialing, completing batch records, putting away finished good inventory (FGI), data entry, equipment maintenance and supply inspections & storage. Other responsibilities include buffer preparation and inspection of incoming buffers into the GMP suite, as well as material preparation for Lyophilization and post lyophilization processes. This role will prepare product/project related documentation and maintain the device history records for all the regulated products and will work closely with product development on new products in order to establish a smooth transition into manufacturing. | 07/24/2025 |
| 862 | Biolog Newark, DE Lab Technician Bachelor’s degree in Life Science or related Exp: 0-3 years |
The Lab Technician supports Biolog’s Lab Services division by performing routine lab tasks that are essential to operations, such as sample handling and processing for ID, discards and restocking inventory. | 07/24/2025 |
| 863 | BioMarin Novato, CA Sr. Analyst, QC Critical Reagents Bachelor’s degree in a related field Exp: 1 year |
The QC Critical Reagents Associate / Sr. Analyst is accountable for maintaining all aspects of the BioMarin Critical Reagents program for commercial products in the global network, including but not limited to maintaining material inventory, generating technical documentation, and supplying materials to the global testing network. Materials in the Critical Reagents program include qualified reagents, reference standards, custom reagents, analytical cell banks and other important materials that require dedicated oversight. The individual prepares trend graphs and analyses for Critical Reagents to support routine requalification activities, regulatory responses, and investigational activities. | 07/24/2025 |
| 864 | Biomerics Winston-Salem, NC Quality Control Engineer, Associate Bachelor’s degree in Engineering Exp: 1-2 years |
The Associate Quality Control Engineer will support the Quality team by assisting with inspection and quality control activities. Learn to apply quality standards and procedures, follow guidelines to perform inspections, and help ensure products meet customer and internal requirements. Work closely with supervisors and production teams while gaining experience in quality methods and tools. | 07/24/2025 |
| 865 | Bio-Rad Irvine, CA Production Chemist I - Temporary Bachelor’s degree in a life science or related field Exp: 0-3 years |
Formulates products and intermediates utilizing biologicals and chemicals of varying properties and characteristics in order to meet specifications | 07/24/2025 |
| 866 | Bio-Techne Minneapolis, MN Scientific Support Associate Bachelor’s degree in Biological Sciences, Biochemistry, or equivalent Exp: 0-2 years |
The responsibilities of this position (Scientific Support Associate, SSA) are to respond to incoming technical inquiries and basic complaints by providing technical assistance on Protein Simple brand instrumentation, software, and applications, with a focus on first-class customer experience. Additional responsibilities will include maintaining technical resources and continual training to stay current on technical information for old and new products. Perform additional duties as assigned. | 07/24/2025 |
| 867 | Bio-Techne Minneapolis, MN Research Associate Bachelor’s degree in biochemistry, biotechnology, or equivalent Exp: 0-2 years |
This position is responsible for purifying proteins and polyclonal/monoclonal antibodies in a GMP Lab, following GMP guidelines. This includes, but is not limited to GMP, ACFP, natural, and other products used by pharma and IVD customers. Purifies proteins and polyclonal/monoclonal antibodies by column chromatography, using a variety of techniques and equipment. Filter, aliquot, and bottling of product using aseptic techniques, and submits to bulk inventory. Documents batch records following GMP guidelines. | 07/24/2025 |
| 868 | Bio-Techne Minneapolis, MN Quality Technician, Hematology Bachelor’s degree in biology, or related field Exp: 0-1 year |
This position will require setup, maintenance, basic troubleshooting, and operation of Hematology analyzers. This position will test hematology products for homogeneity during the bottling process by following established methods. The expectation for this position is to set up and test product on all laboratory instruments and troubleshoot as necessary within 12 months of hire. This position will adhere to safety regulations. Understand the basic ISO protocols and other applicable standards. Perform additional duties as assigned. | 07/24/2025 |
| 869 | Bio-Techne Minneapolis, MN Research Associate, Cell Culture Bachelor’s degree in a biological science Exp: 0-2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins and monoclonal antibodies for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for production, media and supplement preparation, and additional duties as assigned. | 07/24/2025 |
| 870 | Bio-Techne Devens, MA Manufacturing Chemist - Formulation BS or BA degree in Biology, Chemistry or related science discipline Exp: 1-3 years |
The primary responsibilities of the Manufacturing Chemist are to execute formulations and perform in-process testing on customer specific formulations using Good Laboratory Practices and cGMP. In this role you will execute formulation activities independently and under the direction of senior chemists. The Manufacturing Chemist will be responsible for identifying manufacturing issues and effectively communicating those issues to management. | 07/24/2025 |
| 871 | Bio-Techne San Marcos, CA Chemistry Associate Bachelor’s degree in Chemistry, Biochemistry, Biological Science, or related field Exp: 0-2 years |
Responsible for processing and formulation of controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for manufacturing quality products on schedule. General knowledge and basic application of concepts, theories, terminology and practices that apply to manufacturing in a laboratory environment. | 07/24/2025 |
| 872 | Biospectra Bangor, PA Laboratory Systems Technician I Bachelor's degree in Science or related field Exp: 1-3 years |
This position is primarily responsible for reviewing product documentation and verifying laboratory testing. This is an ideal position for an individual with a background in science, laboratory testing in a cGMP/GLP environment, who has an eye for details and likes the idea of being quality assurance for quality control and in so doing assist BioSpectra in ensuring the efficient operation of the Laboratory Services department. | 07/24/2025 |
| 873 | BioStem Technologies Pompano Beach, FL Quality Assurance Associate Bachelor’s degree in Life Sciences, Biology, Biotechnology, or a related field Exp: 0-2 years |
The Quality Assurance Associate plays a key role in supporting daily QA operations within a regulated tissue banking manufacturing environment. This entry-level position is responsible for executing routine quality assurance tasks such as document review, controlled material inspections, logbook audits, and ensuring compliance with internal procedures and applicable regulatory requirements (e.g., 21 CFR 1271, AATB Standards). This is an excellent opportunity for individuals looking to start a career in quality assurance, regulatory compliance, or biotech manufacturing. The QA Associate works closely with experienced QA staff and cross-functional departments to ensure high standards of quality and regulatory adherence are maintained throughout tissue processing operations. | 07/24/2025 |
| 874 | BlueSphere Pittsburgh, PA Cell Therapy Operator/Res. Associate Bachelor’s or Master’s degree in a cell biology, bioengineering, or medical technology-related field, or equivalent Exp: 0-5 years |
The Development team is looking for a motivated team member to join the fast-paced group and contribute to the process and analytical activities to take our TCR products into clinical production. We are looking for someone interested and eager to learn cutting-edge technologies and assist in the tech transfer and production of the products. | 07/24/2025 |
| 875 | Boehringer Ingelheim Gainesville, GA Technician III, Quality Control Bachelor’s Degree Exp: 1-2 years |
To perform, maintain and train on analytical techniques and methods for Quality Control testing required for product release. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees. | 07/24/2025 |
| 876 | Bora Pharmaceuticals Baltimore, MA Analyst I, QC Microbiology - 3rd Shift BS in Microbiology/Biology or related field Exp: 0-2 years |
Responsible for conducting qualitative and quantitative microbial analyses in support of environmental monitoring, cGMP manufacturing and stability of drug products and incoming raw materials. This position supports our 3rd-shift, working 10pm-6:30am, Monday through Friday. | 07/24/2025 |
| 877 | Bora Pharmaceuticals Baltimore, MA Analyst I, QC Analytical-2nd Shift B.S. in Chemistry or related field Exp: 0-2 years |
Perform analytical testing per cGMP in support of raw material, in-process, final product, stability. Typical hours are 10:00 pm – 6:30 am, Monday through Friday. Hours may vary to meet business and training needs. | 07/24/2025 |
| 878 | BostonGene Waltham, MA Laboratory Project Coordinator Bachelor’s degree (B.S.) in biology, Molecular Biology, Biochemistry or related discipline Exp: 1-3 years |
The Project Coordinator plays a critical role in supporting laboratory collaborations with a focus on biospecimen management, regulatory compliance, and data integrity. This position ensures seamless sample handling and documentation for collaboration projects while contributing to system development in alignment with Good Clinical Laboratory Practice (GCLP) standards. | 07/24/2025 |
| 879 | BostonGene Waltham, MA Laboratory Technician, Biospeciman Services Bachelor’s degree in Biological or Life Sciences Exp: 1 year |
The Laboratory Technologist will be responsible for pre-analytical accessioning, processing, and maintaining inventory of clinical blood samples in accordance with established laboratory procedures. This role ensures the integrity of patient samples, supports downstream users in clinical and research operations, and maintains compliance with laboratory quality and regulatory standards. | 07/24/2025 |
| 880 | Bracco Medical Technologies Eden Prairie, MN Quality Systems Specialist II Bachelor’s degree Exp: 1-3 years |
The Quality System Specialist I is responsible for supporting the maintenance of the ACIST Quality Management System. The Quality Assurance Specialist will support the development of a robust quality system in compliance with all relevant standards and regulations at ACIST Medical Systems. | 07/24/2025 |
| 881 | Brainlab Houston, TX Biomedical Engineer (Clinical Specialist) B.S. in Biomedical Engineering, Biomechanical Engineering, Bioengineering, Clinical Engineering, or Nursing Exp: 1-3 years |
Provide on-site consulting and guidance to physicians and Operating Room (OR) personnel by evaluating options and problem-solving during surgery in order to maximize Brainlab product efficiency and usage. Manage and maintain install base, including basic 3rd Party integrations. Analyze and resolve product issues for Brainlab systems at assigned Account(s) via Salesforce through detailed analysis and utilization of critical thinking via technical training and documentation. Utilize engineering expertise to contribute to the quality improvement process by recommending product modifications. Provide clinical case coverage & support for. Complex Cases and Go Live launches (based on availability). Manage the process of driving customer utilization, especially via unique workflows and special applications. Direct and assist Radiology staff in performing necessary scans prior to surgery. Educate/train physicians and hospital personnel, including OR staff, Radiology, Central Sterile Processing, Biomedical and Information Technologies staff, on the use of Image Guided Surgery (IGS) products and services. Develop and conduct training programs for hospital staff enabling them to implement in-house training. Act as primary customer liaison, maintaining contact with customer, assessing satisfaction and usage levels and providing recommendations on this process. Work with the Application Consultant to increase revenue via the sale of spare parts, upgrades, contract renewal, etc. Work closely with the Application Consultant, Area Account Manager, and Marketing Manager on market transparency, upgrade initiatives, demo/evaluations, and Research & Development (R&D) projects. Attend meetings and trade shows to demonstrate and promote IGS products and services. Keep abreast of developments regarding Brainlab and competitive IGS products and services via ongoing training and individual research and analysis. Collaborate and strategize with Regional Support Manager to provide regular content for team calls/meetings (e.g. provide clinical knowledge transfer, share best practices, interesting cases or case set-ups, etc.). Maintain Salesforce documentation of all working hours. Attend IGS Continuing Education annually and maintain annual product certification competency | 07/24/2025 |
| 882 | Brainlab Hinsdale, IL Biomedical Engineer (Clinical Specialist) B.S. in Biomedical Engineering, Biomechanical Engineering, Bioengineering, Clinical Engineering, or Nursing Exp: 1-3 years |
Provide on-site consulting and guidance to physicians and Operating Room (OR) personnel by evaluating options and problem-solving during surgery in order to maximize Brainlab product efficiency and usage. Manage and maintain install base, including basic 3rd Party integrations. Analyze and resolve product issues for Brainlab systems at assigned Account(s) via Salesforce through detailed analysis and utilization of critical thinking via technical training and documentation. Utilize engineering expertise to contribute to the quality improvement process by recommending product modifications. Provide clinical case coverage & support for. Complex Cases and Go Live launches (based on availability). Manage the process of driving customer utilization, especially via unique workflows and special applications. Direct and assist Radiology staff in performing necessary scans prior to surgery. Educate/train physicians and hospital personnel, including OR staff, Radiology, Central Sterile Processing, Biomedical and Information Technologies staff, on the use of Image Guided Surgery (IGS) products and services. Develop and conduct training programs for hospital staff enabling them to implement in-house training. Act as primary customer liaison, maintaining contact with customer, assessing satisfaction and usage levels and providing recommendations on this process. Work with the Application Consultant to increase revenue via the sale of spare parts, upgrades, contract renewal, etc. Work closely with the Application Consultant, Area Account Manager, and Marketing Manager on market transparency, upgrade initiatives, demo/evaluations, and Research & Development (R&D) projects. Attend meetings and trade shows to demonstrate and promote IGS products and services. Keep abreast of developments regarding Brainlab and competitive IGS products and services via ongoing training and individual research and analysis. Collaborate and strategize with Regional Support Manager to provide regular content for team calls/meetings (e.g. provide clinical knowledge transfer, share best practices, interesting cases or case set-ups, etc.). Maintain Salesforce documentation of all working hours. Attend IGS Continuing Education annually and maintain annual product certification competency | 07/24/2025 |
| 883 | Brainlab Denver, CO Biomedical Engineer (Clinical Specialist) B.S. in Biomedical Engineering, Biomechanical Engineering, Bioengineering, Clinical Engineering, or Nursing Exp: 1-3 years |
Provide on-site consulting and guidance to physicians and Operating Room (OR) personnel by evaluating options and problem-solving during surgery in order to maximize Brainlab product efficiency and usage. Manage and maintain install base, including basic 3rd Party integrations. Analyze and resolve product issues for Brainlab systems at assigned Account(s) via Salesforce through detailed analysis and utilization of critical thinking via technical training and documentation. Utilize engineering expertise to contribute to the quality improvement process by recommending product modifications. Provide clinical case coverage & support for. Complex Cases and Go Live launches (based on availability). Manage the process of driving customer utilization, especially via unique workflows and special applications. Direct and assist Radiology staff in performing necessary scans prior to surgery. Educate/train physicians and hospital personnel, including OR staff, Radiology, Central Sterile Processing, Biomedical and Information Technologies staff, on the use of Image Guided Surgery (IGS) products and services. Develop and conduct training programs for hospital staff enabling them to implement in-house training. Act as primary customer liaison, maintaining contact with customer, assessing satisfaction and usage levels and providing recommendations on this process. Work with the Application Consultant to increase revenue via the sale of spare parts, upgrades, contract renewal, etc. Work closely with the Application Consultant, Area Account Manager, and Marketing Manager on market transparency, upgrade initiatives, demo/evaluations, and Research & Development (R&D) projects. Attend meetings and trade shows to demonstrate and promote IGS products and services. Keep abreast of developments regarding Brainlab and competitive IGS products and services via ongoing training and individual research and analysis. Collaborate and strategize with Regional Support Manager to provide regular content for team calls/meetings (e.g. provide clinical knowledge transfer, share best practices, interesting cases or case set-ups, etc.). Maintain Salesforce documentation of all working hours. Attend IGS Continuing Education annually and maintain annual product certification competency | 07/24/2025 |
| 884 | Brainlab Lynchburg, VA Biomedical Engineer (Clinical Specialist) B.S. in Biomedical Engineering, Biomechanical Engineering, Bioengineering, Clinical Engineering, or Nursing Exp: 1-3 years |
Provide on-site consulting and guidance to physicians and Operating Room (OR) personnel by evaluating options and problem-solving during surgery in order to maximize Brainlab product efficiency and usage. Manage and maintain install base, including basic 3rd Party integrations. Analyze and resolve product issues for Brainlab systems at assigned Account(s) via Salesforce through detailed analysis and utilization of critical thinking via technical training and documentation. Utilize engineering expertise to contribute to the quality improvement process by recommending product modifications. Provide clinical case coverage & support for. Complex Cases and Go Live launches (based on availability). Manage the process of driving customer utilization, especially via unique workflows and special applications. Direct and assist Radiology staff in performing necessary scans prior to surgery. Educate/train physicians and hospital personnel, including OR staff, Radiology, Central Sterile Processing, Biomedical and Information Technologies staff, on the use of Image Guided Surgery (IGS) products and services. Develop and conduct training programs for hospital staff enabling them to implement in-house training. Act as primary customer liaison, maintaining contact with customer, assessing satisfaction and usage levels and providing recommendations on this process. Work with the Application Consultant to increase revenue via the sale of spare parts, upgrades, contract renewal, etc. Work closely with the Application Consultant, Area Account Manager, and Marketing Manager on market transparency, upgrade initiatives, demo/evaluations, and Research & Development (R&D) projects. Attend meetings and trade shows to demonstrate and promote IGS products and services. Keep abreast of developments regarding Brainlab and competitive IGS products and services via ongoing training and individual research and analysis. Collaborate and strategize with Regional Support Manager to provide regular content for team calls/meetings (e.g. provide clinical knowledge transfer, share best practices, interesting cases or case set-ups, etc.). Maintain Salesforce documentation of all working hours. Attend IGS Continuing Education annually and maintain annual product certification competency | 07/24/2025 |
| 885 | Arrowhead Pharmaceuticals Madison, WI Associate Scientist, Small Scale Synthesis B.S. Chemistry or Biochemistry degree Exp: 0-2 years |
Arrowhead Pharmaceuticals is seeking an Associate Scientist to join the Discovery Chemistry Department. The successful candidate will primarily focus on oligonucleotide synthesis, purification, analytical chemistry, and contributing to specific program goals. The Associate Scientist will be joining a team of highly motivated and experienced scientists and will contribute to the success of Arrowhead programs. | 07/14/2025 |
| 886 | Arrowhead Pharmaceuticals Verona, WI Associate Manufacturing Scientist I BS or MS in chemistry, biochemistry, engineering, or related scientific field Exp: 0-5 years |
The Associate Manufacturing Scientist supports the production of drug substances and drug products. Their responsibility will focus on the preparation of solutions and reagents by following standard protocols. This technically focused position supports lab work, helps solve problems, and effectively communicates with colleagues. | 07/14/2025 |
| 887 | Arrowhead Pharmaceuticals Verona, WI Associate Scientist, Quality Control B.S. in Chemistry (or related field) Exp: 1-3 years |
This position is within the Quality Control structure under the Quality Department. An Associate Scientist I, Quality Control will support the analytical testing of pharmaceutical raw materials, in-process samples, finished drug substances and drug product, and/or stability sample testing activities for new drug substances and drug products. The Associate Scientist I will also support testing required for GLP Toxicology and cGMP Clinical Trial material release, as well as stability studies. The Associate Scientist is expected to perform several analytical techniques and can make sound scientific decisions under guidance from management. This position reports to QC Laboratory Management. | 07/14/2025 |
| 888 | Artivion Kennesaw, GA Process Engineer Master's degree in Engineering (Mechanical, Chemical, Biomedical, Industrial or related field of engineering) Exp: 1-3 years |
Responsible for providing process engineering support for all product manufacturing departments. Supports manufacturing operations to ensure consistent adherence to the standard operating procedures and business continuity. Initiates process improvement initiatives to improve the efficiency of current manufacturing processes, as well as develop new processes to improve manufacturing efficiency. Supports new product launches by collaborating with other functional areas and providing process engineering expertise during the implementation of processes or equipment. | 07/14/2025 |
| 889 | AskBio Durham, NC Quality Control Analyst I Bachelor’s degree in biology or related field Exp: 0-2 years |
The purpose of the Analyst I, Quality Control (Non-Clinical) is to perform analytical testing to support the release of Non-Clinical grade rAAV vector lots manufactured in various AskBio departments (including, Pre-Clinical Manufacturing, Process Development, MSAT) and external partners. The rAAV vectors tested/characterized by the team will support capsid technology development, intellectual property portfolio, and internal progression of early-stage gene therapy programs. | 07/14/2025 |
| 890 | Astellas Pharma Sanford, NC Specialist, QA Validation M.S. degree in Biological/Physical/Chemical sciences, engineering, or equivalent Exp: 1-3+ years |
The Specialist, QA Validation will be primarily responsible for the implementation, execution and assessment of quality systems, procedures, and records to support compliant GMP operations. This position works closely with Validation, Engineering, Manufacturing, Quality Control, Facilities, and Automation. | 07/14/2025 |
| 891 | Astellas Pharma South SF, CA Research Associate II, Discovery Bioscience Master's degree in a life science, chemical engineering or related discipline Exp: 1+ years |
The Research Associate will be an integral member of the Vector Bioscience team and assist in developing, characterizing, and producing AAV vectors. The Research Associate will work at our South San Francisco R&D laboratories, supporting and collaborating with various research and development groups. | 07/14/2025 |
| 892 | AstraZeneca Philadelphia, PA Automation Engineer BA/BS Engineering/Life Sciences Exp: 0-5+ years |
Are you ready to take on the challenge of crafting the future of automation in a multifaceted environment? As an Automation Engineer, you'll be at the forefront of technological advancements, providing technical mentorship and support for equipment at our Philadelphia and Bensalem sites. You'll play a pivotal role in the procurement of new equipment, leading projects and collaborating with IT, operations, facilities, and maintenance teams to implement changes. | 07/14/2025 |
| 893 | AstraZeneca Mount Vernon, IN PET Formulation Senior Process Engineer Master's degree required, preferably in Science, Chemical Engineering, or other related technical discipline. Exp: 1 year |
Are you ready to break new ground and leave a collective legacy? As a PET Formulation Senior Process Engineer, you will provide technical support for formulation, investigating and correcting process-related problems and deviations from standards. You will serve as a Subject Matter Expert for multiple processing operations and provide technical leadership within the Process Engineering team. You may also lead Technology Transfers to and from the site. | 07/14/2025 |
| 894 | August Bioservices Nashville, TN Manufacturing Technician II/III Bachelor's degree in biological, chemical sciences, or engineering Exp: 1+ years |
August Bioservices is seeking to hire experienced manufacturing technicians to support our growing formulations and filling teams. Headquartered in Nashville, TN – one of the fastest-growing and most exciting cities in the United States – August Bioservices is a privately-owned, high-growth, and high-impact Contract Development Manufacturing Organization (CDMO). As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our work is instrumental in helping to develop molecules today that can become the life-changing therapies of tomorrow. For those seeking dynamic opportunities, rewarding career paths and a chance to make a difference in global health, come grow with August! | 07/14/2025 |
| 895 | August Bioservices Nashville, TN Microbiologist I B.A./ B.S in Biology (or related) Exp: 0-2 years |
August Bioservices is looking for a Quality Control team member that is passionate and driven professionally. August Bioservices desires a team member eager to work in an environment where people are motivated to do their best for the company and its clients. Reporting to the Manager, Microbiology, the Microbiologist I will be responsible for performing biological assays of raw materials, in-process samples, finished product, and environmental monitoring samples. He/she will work with microbiology personnel to assure test results, procedures, and methods are written, maintained, executed, and approved in accordance with approved SOPs and regulatory requirements. | 07/14/2025 |
| 896 | Avalign Akron, OH Quality Engineer BS in an engineering science Exp: 0-3 years |
The Quality Engineer is responsible for supporting the organization to ensure quality and production goals are met. The Quality Engineer will utilize an engineering approach to improve manufacturing efficiencies and ensure quality standards of all products are met. | 07/14/2025 |
| 897 | Avalign Greenwood, IN Quality Engineer BS in an engineering science Exp: 0-3 years |
The Quality Engineer is responsible for supporting the organization to ensure quality and production goals are met. The Quality Engineer will utilize an engineering approach to improve manufacturing efficiencies and ensure quality standards of all products are met. | 07/14/2025 |
| 898 | Avantor Carpinteria, CA Process Engineer II B.S. in engineering, chemical Exp: 1-3 years |
Avantor is looking for an engaging and motivated Process Engineer to optimize our NuSil team, delivering results against some of the most complex business and technology initiatives. This role will be a full-time position based out of our Carpinteria, CA. You will have the opportunity to be responsible for all phases of medium-scale assigned process improvement projects, ensuring the successful conclusion of all phases within an appropriate time and at appropriate cost. If you are passionate about expanding your knowledge base and making a positive impact – let’s talk! | 07/14/2025 |
| 899 | Avantor Bakersfield, CA Process Engineer II B.S. in engineering, chemical Exp: 1-3 years |
Avantor is looking for an engaging and motivated Process Engineer to optimize our NuSil team, delivering results against some of the most complex business and technology initiatives. This role will be a full-time position based out of our Bakersfield, CA facility with occasional travel to our sister site in Carpinteria, CA. You will have the opportunity to be responsible for all phases of medium-scale assigned process improvement projects, ensuring the successful conclusion of all phases within an appropriate time and at appropriate cost. If you are passionate about expanding your knowledge base and making a positive impact – let’s talk! | 07/14/2025 |
| 900 | Avantor Sant Louis, MO Quality Control Lab Analyst Bachelor’s degree in Biology, Chemistry, Biochemistry, or other science Exp: 0-3 years |
Perform microbiological assays including microbial limits testing, endotoxin testing, and environmental monitoring. Prepare and process raw material, in-process samples, and finished products for microbiological testing. Operate and maintain laboratory equipment such as autoclaves, incubators, laminar flow hoods, and microbial identification systems. Ensure equipment calibration is performed per established schedules. Conduct routine environmental monitoring of laboratory and production areas, including water and viable air monitoring. Maintain laboratory inventory and order consumables as needed. Maintain accurate records and ensure proper documentation of all laboratory activities, test results and events. | 07/14/2025 |
| 901 | Aviva Systems Biology San Diego, CA Research Associate I/II, Molecular Biology B.S. or M.S. in life science or related subject Exp: 1+ years |
Aviva Systems Biology is a fast paced, mid stage life sciences research tools company located in San Diego, CA. We commercialize life science tools and reagents for research, drug discovery, and diagnostics. Perform routine molecular biology techniques such as PCR, transfection, cell lysis. Perform small-scale bacterial, fungal, and mammalian cell culture using aseptic techniques. Operate incubator/shakers, centrifuges, and other laboratory equipment used in protein production. Use electrophoresis and chromatography systems for biomolecule analysis or purification. Prepare chemical solutions required for production processes. Analyze Sanger sequence data for validation of expression constructs | 07/14/2025 |
| 902 | Aviva Systems Biology San Diego, CA Research Associate I/II, Biochemistry B.S. or M.S. in life science or related subject Exp: 1+ years |
Aviva Systems Biology is a fast paced, mid stage life sciences research tools company located in San Diego, CA. We commercialize life science tools and reagents for research, drug discovery, and diagnostics. Perform routine biochemistry techniques such as protein expression, purification, and characterization by SDS-PAGE. Perform small-scale bacterial, fungal, and mammalian cell culture using aseptic techniques. Operate incubator/shakers, centrifuges, and other laboratory equipment used in protein production. Use electrophoresis and chromatography systems for biomolecule analysis or purification. Prepare chemical solutions required for production processes. Analyze Sanger sequence data for validation of expression constructs | 07/14/2025 |
| 903 | Axogen Vandalia, OH Quality Analyst - 1st Shift Bachelor’s Degree in a Life Science discipline, engineering, or in a related field Exp: 0-2 years |
The Quality Analyst performs quality control (QC) inspections and dispositions of materials and products according to specifications. This role will perform QC inspection using measuring instruments (when applicable) and inspection methods. The role ensures any non-conforming materials or products that are identified are managed according to Axogen’s Quality System. The Quality Analyst is responsible for following all Axogen policies and procedures to ensure compliance with applicable with FDA, state OSHA and ISO regs and standards. Employees within this role will performs a variety of tasks under limited supervision. | 07/14/2025 |
| 904 | Axogen Vandalia, OH Quality Analyst - 2nd Shift Bachelor’s Degree in a Life Science discipline, engineering, or in a related field Exp: 0-2 years |
The Quality Analyst performs quality control (QC) inspections and dispositions of materials and products according to specifications. This role will perform QC inspection using measuring instruments (when applicable) and inspection methods. The role ensures any non-conforming materials or products that are identified are managed according to Axogen’s Quality System. The Quality Analyst is responsible for following all Axogen policies and procedures to ensure compliance with applicable with FDA, state OSHA and ISO regs and standards. Employees within this role will performs a variety of tasks under limited supervision. | 07/14/2025 |
| 905 | Axogen Vandalia, OH Quality Analyst - 3rd Shift Bachelor’s Degree in a Life Science discipline, engineering, or in a related field Exp: 0-2 years |
The Quality Analyst performs quality control (QC) inspections and dispositions of materials and products according to specifications. This role will perform QC inspection using measuring instruments (when applicable) and inspection methods. The role ensures any non-conforming materials or products that are identified are managed according to Axogen’s Quality System. The Quality Analyst is responsible for following all Axogen policies and procedures to ensure compliance with applicable with FDA, state OSHA and ISO regs and standards. Employees within this role will performs a variety of tasks under limited supervision. | 07/14/2025 |
| 906 | Axogen Tampa, FL Laboratory Technician, R&D Bachelor’s degree Exp: 1 year |
The Laboratory Technician plays a key role in supporting the daily operations of Axogen’s R&D laboratory. This position is responsible for executing routine experiments and testing, preparing and analyzing biological and tissue-based samples, and maintaining laboratory equipment and supplies. The Laboratory Technician will ensure safe handling and disposal of hazardous and biohazardous materials, maintain accurate records, and contribute to the continuous improvement of lab workflows. Success in this role requires strong attention to detail, a collaborative mindset, and the ability to work effectively in a regulated environment. | 07/14/2025 |
| 907 | B. Braun Irvine, CA QC Chemistry Assoc I Bachelor's Degree Exp: 0-2 years |
Perform routine laboratory analysis of In-Process, finished product, raw material, stability samples and environmental monitoring according to established specifications and procedures using wet chemistry techniques or various laboratory apparatus and instruments (e.g. HPLC, UV/Visible Spectrophotometer, FTIR, TOC, pH meter etc.) in compliance with B. Braun, cGMP, GLPs, SOPs, USP and FDA guidelines. | 07/14/2025 |
| 908 | B. Braun Daytona Beach, FL QC Lab Tech II-Chemistry Bachelor's degree Exp: 1-2 years |
Performs a variety of quality control tests on products at various stages of the production process to ensure compliance with quality and reliability standards. Records statistical data. Analyzes data and writes summaries to validate or show deviations from existing standards. Recommends modifications to existing or suggests new, standards, methods and procedures. | 07/14/2025 |
| 909 | B. Braun Daytona Beach, FL QC Lab Tech II-Microbiology Bachelor's degree Exp: 1-2 years |
Performs a variety of quality control tests on products at various stages of the production process to ensure compliance with quality and reliability standards. Records statistical data. Analyzes data and writes summaries to validate or show deviations from existing standards. Recommends modifications to existing or suggests new, standards, methods and procedures. | 07/14/2025 |
| 910 | BA sciences Salem, NH Sample Control Technician Bachelor’s degree in a scientific discipline Exp: 0-2 years |
The Sample Control Technician is responsible for ensuring that all samples are entered into the Laboratory Information Management System (LIMS) and made available to the lab staff in a timely manner. Assists with the coordination and maintenance of stability studies as directed and in accordance to FDA, cGMP, and Boston Analytical's Standard Operating Procedures. This position reports to the Manager of Sample Control. | 07/14/2025 |
| 911 | BA sciences Salem, NH Chemist II Bachelor’s degree in Chemistry or a related discipline Exp: 1+ years |
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and BA Sciences. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. | 07/14/2025 |
| 912 | BA sciences Salem, NH Microbiologist I, MB BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The Microbiologist I conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 07/14/2025 |
| 913 | BA sciences Salem, NH Microbiologist I, VD BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The Microbiologist conducts validation and feasibility testing for quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and BA, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 07/14/2025 |
| 914 | BA sciences Salem, NH Microbiologist QC I BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The QC Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 07/14/2025 |
| 915 | Bachem Vista, CA Chemist Bachelor’s degree in chemistry or related scientific field Exp: 0-2 years |
The Chemist function is to work in a cGMP regulated environment manufacturing active pharmaceutical products (APIs) as well as performing related activities at Bachem. | 07/14/2025 |
| 916 | Bachem Torrance, CA Chemist Bachelor’s degree in chemistry or related scientific field Exp: 0-2 years |
The Chemist function is to work in a cGMP regulated environment manufacturing active pharmaceutical products (APIs) as well as performing related activities at Bachem. | 07/14/2025 |
| 917 | Balt Irvine, CA Quality Engineer I Bachelor’s degree in engineering or science discipline. Exp: 0-2 years |
This position is responsible for the implementation, maintenances, and sustainment of the Balt USA’s quality management system in accordance with procedures compliant with 21 CFR Part 820 and ISO 13485 requirements. Develops and analyzes quality systems procedures and documents by leveraging regulatory requirements and continuous improvement principles. Upholds compliance efforts for NCMR, CAPA, quality audits, procedure adherence, GMP enforcements and applies continuous improvement principles to support kaizen events, problem solving, fixturing improvement, and scrap reduction. Support efforts for supplier quality management and supplier development as part of nonconforming corrective action. Works with various employees to develop, improve, and stabilize quality process controls. Monitors quality issues to help determine root cause and implement corrective action. Works with all functions to achieve quality and business goals. Compiles and writes training material and conducts training sessions on quality control activities. | 07/14/2025 |
| 918 | Baxter Marion, NC Quality Lab Associate I - Endotoxin Master’s Degree in biological sciences Exp: 0-3 years |
Conduct microbiological analysis on raw materials, solution, and water samples following approved Standard Operating Procedures in an accurate and timely manner. | 07/14/2025 |
| 919 | Baxter Round Lake, IL Senior Mechanical Engineer Master's degree in Mechanical Engineering or a related field Exp: 1+ years |
Are you ready to make a difference in the world of healthcare? Join our innovative team as aSenior Mechanical Engineer, where your creativity and technical expertise will help shape the future of our infusion system product portfolio. In this role, you will tackle exciting challenges, develop cutting-edge solutions, and contribute to life-saving technologies that have a real impact on patients' lives. If you’re passionate about engineering and eager to work in a dynamic environment, we want to hear from you! As a Senior Mechanical Engineer, you will be at the forefront of product development, working on both new and existing infusion systems. | 07/14/2025 |
| 920 | Baxter Round Lake, IL Quality Lab Associate I - 3rd Bachelors degree in Chemistry or Science related degree Exp: 6+ months |
The Position encompasses the biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs. This is a 3rd shift position, Monday-Thursday, 10:00 pm - 8:30 am. A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials. | 07/14/2025 |
| 921 | Baxter Round Lake, IL Research Associate II - LC-MS Master's degree in relevant scientific discipline (chemistry, pharmaceutical sciences) Exp: 1+ years |
As a Research Associate you will effectively contribute to a variety of projects within the R&D team and development & validation of LC-MS methods targeting specifically nitrosamines. Conduct routine/non-routine research and design experiments. Participate in project team and work in collaboration with other R&D groups of Formulation Development, Quality Control, Process Development, Manufacturing, etc | 07/14/2025 |
| 922 | Baxter Hayward, CA Tech IV, MNF Formulation Bachelor’s degree Exp: 1 year |
The Manufacturing Technician IV is responsible for assisting the supervisor in organizing, scheduling and directing other team members as well as execute all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Manufacturing Technician IV may be the main interface with other functional departments to resolve issues. Represent the department in cross- functional team as necessary. | 07/14/2025 |
| 923 | Baxter Marion, NC Quality Lab Associate I - Environmental Monitoring B.S. degree in Microbiology, Biology, or related science Exp: 0-2 year |
Supports the environmental monitoring program by performing testing such as surface testing, viable air monitoring, and air total particle counts. Responsible for conducting routine risk assessments and HEPA filter inspections in cleanrooms. | 07/14/2025 |
| 924 | Baxter Round Lake, IL Quality Lab Associate I - 2nd Shift Bachelors degree in Chemistry or Science related degree Exp: 6+ months |
The Position encompasses the biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs. This is a 2nd shift position, Sunday - Wednesday, 2:00 pm - 12:30 am. A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials. | 07/14/2025 |
| 925 | Aktis Oncology Boston, MA Sr/Clinical Trial Associate - Clinical Ops Bachelor’s degree in life sciences, healthcare, or related field Exp: 1-3 years |
The Clinical Trial Associate (CTA) will support the planning, execution, and documentation of clinical trials involving radiopharmaceutical agents. Working under the direction of the Clinical Trial Manager or Clinical Operations Lead, the CTA will assist with key trial activities including study start-up, tracking, document management, and coordination with external vendors and clinical sites. This role is critical for maintaining quality, compliance, and operational efficiency across clinical programs. | 07/09/2025 |
| 926 | Alamar Biosciences Fremont, CA Manufacturing Associate I B.S. or B.A. degree in Biology, Chemistry or equivalent Exp: 1+ years |
We are seeking a highly disciplined, energetic, and results-driven candidate to join our Operations team as Manufacturing Associate I. Manufacturing Associate I is responsible for executing production orders to meet daily production schedule under some supervision. Job responsibilities include the manufacturing of biological reagents and finished products such as reagent formulations, antibodies conjugation, components lyophilization, and filling and assembly of final products. Experience working under ISO 13485 and/or current Good Manufacturing Practice (cGMP) in a biotechnology or pharmaceutical industry is highly preferred. | 07/09/2025 |
| 927 | Alamar Biosciences Fremont, CA Manufacturing Associate I - Temporary B.S. or B.A. degree in Biology, Chemistry or equivalent Exp: 1+ years |
We are seeking a disciplined, energetic, and fast learning candidate to join our Operations team as Manufacturing Associate I. Manufacturing Associate I is responsible for completing production orders in accordance with the daily production schedule. Job responsibilities include the manufacturing of biological reagents and finished products such as reagent formulations, antibodies conjugation, components lyophilization, and filling and assembly of final products. Experience working under ISO 13485 and/or current Good Manufacturing Practice (cGMP) in a biotechnology or pharmaceutical industry is highly preferred. | 07/09/2025 |
| 928 | Alcami Wilmington, NC Scientist II - Chemistry Masters degree in Chemistry, Biochemistry, or related field Exp: 0+ years |
The Scientist II (Chemistry) is accountable for driving results in a fast-paced environment by performing analytical routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. For this Scientist II (Chemistry) position, ICP, HPLC, TOC, UV, osmolality, density, and pH are commonly employed in the described testing in addition to other key methodologies such as KF and titration. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company) and may also assist with method development / method validation projects. | 07/09/2025 |
| 929 | Alcami Morrisville, NC Manufacturing Technician II - Sterile Injection (3rd Shift) Bachelor’s degree Exp: 1-2 years |
The Manufacturing Technician II (Compound/Fill/Finish) is accountable for results in a fast-paced environment and assists with the manufacturing of sterile injectable products in vial and syringe configurations for clinical/commercial distribution. The Manufacturing Tech II is a key role responsible for executing advanced production tasks involving compound, fill and finish processes for sterile injectable pharmaceutical products executed via aseptic isolator technology. This position entails a high level of technical expertise in aseptic processes requiring single-use components, ability to troubleshoot, and responsibility for maintaining quality and compliance with Good Manufacturing Practices (GMP). The Manufacturing Tech. II performs the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Tech. II employs acceptable techniques while working in manufacturing environments, including PPE gowning. The candidate must have the ability to learn specific department procedures, have a general understanding of Good Documentation Practices (GDP) and GMP, and follow directions from leadership/peers to ensure manufacturing goals are met. | 07/09/2025 |
| 930 | Alcami Charleston, SC Pharmaceutical Manufacturing Technician - 3rd Shift Bachelor's degree in chemical engineering Exp: 1+ years |
The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employ acceptable techniques while working in manufacturing environments, including PPE gowning. The Manufacturing Technician I works collaboratively to support other manufacturing areas as required. | 07/09/2025 |
| 931 | Alcami Morrisville, NC Manufacturing Technician I - Sterile Injection (2nd Shift) Bachelor’s degree Exp: 1-2 years |
The Manufacturing Technician I (Compound/Fill/Finish) is accountable for results in a fast-paced environment and assists with the manufacturing of sterile injectable products in vial and syringe configurations for clinical/commercial distribution. The Manufacturing Tech I is a key role responsible for executing advanced production tasks involving compound, fill and finish processes for sterile injectable pharmaceutical products executed via aseptic isolator technology. This position entails a high level of technical expertise in aseptic processes requiring single-use components, ability to troubleshoot, and responsibility for maintaining quality and compliance with Good Manufacturing Practices (GMP). The Manufacturing Technician I performs the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Tech. I employs acceptable techniques while working in manufacturing environments, including PPE gowning. The candidate must have the ability to learn specific department procedures, have a general understanding of Good Documentation Practices (GDP) and GMP, and follow directions from leadership/peers to ensure manufacturing goals are met. | 07/09/2025 |
| 932 | Alcami Morrisville, NC Scientist II - Compendial Testing, Raw Material Master’s degree Exp: 0+ years |
The Scientist II is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Scientist II / III may also be required to work on method development/method validation projects. For this position, HPLC, dissolution and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company). | 07/09/2025 |
| 933 | Alcon Johns Creek, GA Sr. Associate M.S. Exp: 0+ years |
As a Senior Associate, you will lead research efforts focused on the development of next generation contact lenses and innovative materials for medical devices. This role requires a strong expertise in material science, especially in understanding the structure-property relationship of materials and demands an innovative mindset to drive research forward. | 07/09/2025 |
| 934 | Alcon Johns Creek, GA Sr. Associate, Automation and Control Engineering M.S. Exp: 0+ years |
s a Sr. Associate, Automation and Control Engineering, supporting our supporting our Engineering Manufacturing Systems team, you will be trusted to design, implement, install, analyze and/or optimize manufacturing processes, procedures, equipment, and programming. The ideal candidate will also have expertise in PLC and automation controls, ensuring seamless integration and functionality of mechatronic systems to best support our 24/7 operation at Johns Creek, GA. | 07/09/2025 |
| 935 | Alcon Johns Creek, GA Opto-Mechanical Engineer M.S. Exp: 0+ years |
As an Opto-Mechanical Engineer, you will collaborate with design engineers, metrology engineers, chemistry and process scientists, and clinicians, to deliver state-of-the-art opto-mechanical, mechanical and optical designs supporting new product development for ophthalmic medical device products. This role will be in located in Johns Creek, GA. The Opto-Mechanical Engineer designs, models, analyzes, and tests optical, electro-optical, and opto-mechanical systems and components, including sensors, lasers, fiber-optics, and telecommunications products. Conducts research and development into phases of physical optics and geometric optics, lasers, laser characteristics, laser maintenance, and broadband optical sources. Applies research of complex optical systems to achieve desired optical outcomes. Develops component specifications, tolerances, simulations and tests procedures for electro-optical systems and components. Uses design-to-cost models, six sigma methodology, and other methods to assure and verify optical design requirements are met. | 07/09/2025 |
| 936 | Aldevron Madison, WI Associate Scientist II - Upstream PD Bachelor's or Master's degree in biology, biotechnology, molecular biology, biochemistry, chemistry, or a closely related field Exp: 0-1+ years |
The Associate Scientist II position is part of the Upstream Process Development team in the Protein Business Unit of Aldevron. This is an on-site position at the facility located in Madison, WI. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Technical Operations team and report to the Upstream Process Development manager. Your responsibilities will revolve around developing processes to produce recombinant proteins using microbial host expression systems. | 07/09/2025 |
| 937 | Aldevron Fargo, ND Analyst I QC Environmental Monitoring Bachelor’s degree in microbiology or related scientific field Exp: 0-1 years |
The Analyst I Quality Control Environmental Monitoring is responsible for sampling, detecting, quantifying, and identifying possible contaminants that may interfere with the quality of the product during the different stages of the manufacturing process. This position reports to the QC Microbiology Supervisor and is part of the Quality Control Environmental Monitoring Team located in Fargo, ND and will be an on-site role. | 07/09/2025 |
| 938 | Alkermes Wilmington, OH Manufacturing Associate I-OSD Nights Bachelor's degree Exp: 0-1 years |
This entry-level position involves working with a small team in a GMP environment to manufacture commercial and/or clinical-scale batches. | 07/09/2025 |
| 939 | Alloy Therapeutics Waltham, MA Research Associate, Oligonucleotide Discovery B.S. or M.S. degree in Biology or related science Exp: 1-3 years |
As a Research Associate, you will work within the Genetic Medicines team in Waltham, MA. You will also collaborate with internal/external partners on nucleic acid drug discovery projects to ensure timely execution of the experiments, and delivery of high-quality data. This role will have an autonomy owning various stakeholders, projects, and tasks in a dynamic start-up environment while keeping up the pace of Alloy. This role will report to Senior Scientist with autonomy owning various stakeholders, projects, and tasks in a dynamic start-up environment while keeping up the pace of Alloy. | 07/09/2025 |
| 940 | Almac Souderton, PA Validation Officer - ENG Bachelor’s Degree Exp: 1 year |
Almac Group is currently seeking a Validation Officer for our Souderton, PA location. The Validation Officer will work as part of the Quality department, you will be responsible for coordinating validation activities, at any Almac Clinical Services site, to ensure that simple equipment, facilities, and processes (E/F/P) achieve compliance with business and regulatory requirements and to ensure their validated status is maintained throughout their operational lifetime. | 07/09/2025 |
| 941 | Almac Audubon, PA QC Inspector Grade 1 Bachelor’s Degree Exp: 1 year |
Almac is seeking a Quality Control Inspector Grade 1 for our Audubon, Pa. location. The Quality Control Inspector Grade 1 will be responsible for upholding the high standard of GMP within the business. The successful candidate will be expected to perform in process checks, environmental monitoring, sampling and testing of packaging components and medicinal bulk, and assessment of clean down and line clearances of production rooms and equipment. | 07/09/2025 |
| 942 | Altasciences Columbia, MO Scientist, LCMS /Bachelor’s degree in Immunology/ Biology/ Chemistry or equivalent discipline Exp: 6 months |
You will assist in daily activities and operation of the Laboratory Sciences department including equipment maintenance, stocking supplies and general cleaning. You will also support and perform data collection activities including primarily focused on mass-spectrometry. | 07/09/2025 |
| 943 | Altasciences Everett, WA Pathology Associate I, II, III Bachelor of Science (B.S.) or Bachelor of Arts (B.A.) Exp: 6 months-1 year |
To provide high quality and timely processing of pathological specimens through gross examinations, necropsies, tissue trimming and tissue processing as specified in company protocols and SOPs. | 07/09/2025 |
| 944 | Altasciences Everett, WA Laboratory Supervisor Bachelor's degree in a scientific discipline. Exp: 1-3 years |
Responsible for managing Research Associates and assisting Scientists on studies/projects. Assists with training other laboratory staff in technical procedures. Assist with evaluating and optimizing the utilization of laboratory resources to attain operational goals, meet study deadlines, and deliver quality results. Works with Laboratory Sciences Senior Manager of Operations in formulating current and long-range plans, objectives and policies. | 07/09/2025 |
| 945 | Alveo Alameda, CA Scientist II BA/BS degree in Biochemistry, Molecular Biology, Microbiology or related field Exp: 1-4 years |
Alveo Technologies is looking for an Assay Development and Verification Scientist II to support ongoing Validation and Verification efforts for projects in disease detection. The Scientist will assist in planning and executing protocols and conducting experiments at the bench to meet objectives. This position will review, understand and follow the instructions, protocols and SOPs. | 07/09/2025 |
| 946 | American Regent Brea, CA Production Supervisor Bachelor’s in Pharmaceutical Science, Chemistry, [Micro] Biology, Engineering, or a related field Exp: 1-3 years |
This position is a member of the Manufacturing Team. The Manufacturing Team is responsible for activities associated with the manufacture of safe, effective, and sterile pharmaceuticals in accordance with company SOPs, policies and cGMPs. The Manufacturing Team ensures aseptic and sanitary conditions are maintained where required, appropriate manufacturing area and equipment records are neat and accurate and safe, effective, and professional behavior is displayed at all times. In conjunction with Production Management the Manufacturing Team provides input and assistance to other Departments as needed, playing a critical role in maintaining production schedules and meeting Company goals. The Production Supervisor will be able to oversee all aspects of the Manufacturing Process. The Manufacturing Process includes component prep, aseptic cleaning, compounding, filtration, and filling in accordance with established production records in a concerted effort to manufacture sterile liquid pharmaceuticals. The Production Supervisor will be able to perform, oversee and provide signatory approval for all activities associated with the manufacturing process. The Production Supervisor will be able to provide direction, training and mentorship to all junior team members as needed. The Production Supervisor will be the responsible person for the proper use of batch documentation. The Production Supervisor will be able to troubleshoot most of the manufacturing process and equipment and where necessary make adjustments and minor repairs during setup and during operations. | 07/09/2025 |
| 947 | Amneal Brookhaven, NY Scientist, Quality Control Master Degree (MBA) Microbiology or related science discipline Exp: 1+ years |
Performs microbiological analysis of water, raw materials, in-process and finished pharmaceutical products, including products on stability, according to written methods or compendial methods as applicable, material specifications, using analytical techniques such as aseptic techniques, plating techniques, dilution and enumersastion techniques adhering to company policies as identified in standard operating procedures (SOPs). Prepares samples for analysis involving aseptic techniques and proper sample handling techniques as applicable. Perform Identification of organisms. | 07/09/2025 |
| 948 | Amneal Piscataway, NJ Validation Engineer Bachelors Degree (BA/BS) BS: in Pharmaceutical manufacturing, Engineering, Science or relevant field Exp: 1 year |
The Validation Engineer is responsible for performing validation and Engineering activities, conducting development studies, analyzation and assist in improving pharmaceutical systems and processes. | 07/09/2025 |
| 949 | AstraZeneca Waltham, MA Scientist, Bioscience BS in Biology, Biotechnology or other relevant area Exp: 1-2 years |
Discovery Sciences applies deep technical expertise in specialist technologies to support the delivery of targets and molecules to the early AstraZeneca pipeline. Targets are identified through our human genomics and functional genomics efforts, employing the latest technologies in genome editing and advanced cell model development. Once identified and validated, we work with therapy area project teams to identify novel small molecule effectors of these targets using our integrated sample management and platform screening groups. As the new range of targeted therapeutics moves towards the clinic, we are placing an increased emphasis on understanding the links between the chosen molecular target, disease type/stage, and drug responses. Key to this is the provision of high-quality cellular models for research. The GCB team is critical for delivering these cellular models and developing methods to prepare primary cell lines for projects aligned with our strategic objective of increasing the translatability of the cell models used in research. We are now offering an exciting opportunity for a dedicated and highly motivated individual to join us in the role of Scientist, GCB. | 07/09/2025 |
| 950 | Andelyn Biosciences Columbus, OH Environmental Monitoring Technician Bachelor’s degree, a background in the life sciences, biotechnology, or gene therapy industries Exp: No exp |
The Environmental Condition Team is responsible for the activities associated with the manufacture of safe, effective pharmaceuticals in accordance with company SOPs, and policies. The Environmental Monitoring Team works in concert with and assists the manufacturing department and plays a critical role in ensuring environmental control of the cleanroom. The Environmental Monitoring Technician position is primarily responsible for performing environmental monitoring activities including air, surface, and personnel monitoring within the cleanroom. In addition, to sampling critical utilities throughout the GMP facility.. | 07/09/2025 |
| 951 | Anika Bedford, MA QC Incoming Inspector I Bachelor’s degree Exp: 0-1 years |
The QC Incoming Inspector completes all activities required to approve raw materials for use in product manufacture on the second shift. The position also performs inspection activities during in-process manufacturing for second shift. | 07/09/2025 |
| 952 | Anika Bedford, MA QC Microbiologist I BS in microbiology, biology or related science Exp: 1+ years |
Responsible for all microbiological and some analytical testing of production materials under GMP conditions. Responsible for process and equipment validation (autoclave and depyrognenation oven) in cooperation with Engineering and R&D (New Product Sterility and LAL validation.) | 07/09/2025 |
| 953 | Antheia Menlo Park, CA Downstream Process Engineer I B.S. in Chemical Engineering or relevant area of study Exp: 0-2 years |
Antheia is seeking a junior Process Engineer to join our Downstream Processing team. In this role, you will help develop and scale processes to separate and purify bio-derived Key Starting Materials and APIs, moving from bench to pilot and commercial scales. You will gain an understanding of how impurities behave, how products degrade over time, and how to design processes that stay within target cost and performance ranges. You will support day-to-day unit operations, collect and analyze data, and help define key parameters for each step. Hands-on lab skills in sample preparation, as well as experience with liquid-solid and liquid-liquid separations, are important. You’ll work closely with cross-functional teams—including Biology, Analytics, Operations, Quality, and Regulatory—to help create efficient, reliable processes that deliver high-quality products on schedule. | 07/09/2025 |
| 954 | Applied Medical Rancho Santa Margarita, CA Machine Design Engineer, Automation Bachlor's degree in Mechanical Engineering or in a related field Exp: 1 year |
Are you a visionary Design Engineer? Join Applied Medical and be at the forefront of revolutionizing medical device manufacturing. As part of our Automation team, you will be at our global U.S. headquarters, pioneering cutting-edge machines, collaborating across departments, and leading the way in cost reduction, optimizing manufacturing processes. As a Design Engineer, you will play a vital role in supporting the development of automated machines or automated processes for our in-house medical device manufacturing. It's your chance to make an enduring impact on the future of healthcare. | 07/09/2025 |
| 955 | Applied Medical Rancho Santa Margarita, CA Process Engineer Bachelor’s degree in Mechanical, Biomedical, Industrial, or Manufacturing Engineering Exp: 1-10 years |
As a Process Engineer, you will work within the Group Process Development team and use skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. The Process Engineer’s primary responsibilities are debugging, observing, and expediting shop orders. You will assist with developing and updating engineering documents and investigating new tooling, materials, manufacturing processes, and technologies. | 07/09/2025 |
| 956 | Applied Medical Rancho Santa Margarita, CA Complaint Evaluation Engineer Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, Electrical Engineering or a similar engineering discipline Exp: 1 year |
Collaboration is a fundamental part of our organization's culture and is essential to our continued success. As such, the successful candidate for this position is expected to work on-site, enabling them to engage fully with colleagues and contribute to cross-functional initiatives. Therefore, the ability to work collaboratively and contribute to a positive and supportive team environment is a key requirement for this role. As a Complaint Evaluation Engineer, you will evaluate the performance of products returned by the customer. | 07/09/2025 |
| 957 | Applied Medical Lake Forest, CA Plastics Process Engineer Bachelor’s degree in Plastics, Manufacturing, Polymer, Materials, Mechanical Engineering, or a related engineering field Exp: 1 year |
Join Applied Medical and contribute to advancing the future of medical device manufacturing. As a Plastics Process Engineer, you will play a hands-on role in developing, optimizing, and supporting manufacturing processes with a strong focus on injection molding, heat treating, and complex part fabrication. This position offers a dynamic environment where engineers are deeply involved on the production floor, working closely with mold makers, process technicians, and production teams to make a direct impact on patient care. This is a project-management oriented role requiring strong coordination and follow-through. | 07/09/2025 |
| 958 | Applied Medical Cleveland, OH Materials Engineer Bachelor’s or Master’s degree in polymer science/engineering, chemistry, chemical engineering, materials science, or any other related fiel Exp: 0-2+ years |
As a Materials Engineer, you will be responsible for creating, monitoring, and controlling material related projects. You will provide materials expertise in projects that partner with design and manufacturing engineers and ensure manufacturability and performance of devices through proper material selection and processing. Additional projects will be in partnership with Quality Assurance in test method development and material characterization to help drive continuous improvement. The individual in this position will interface multiple R&D projects including design, preparation and execution of experiments, analysis and presentation of results, and coordination with external characterization laboratories. You will be expected to maintain and ensure a safe, organized, and efficient work environment. The materials tested in the laboratory will include a variety of thermoplastics, thermosets, coatings, adhesives, and silicone rubbers. | 07/09/2025 |
| 959 | Argonaut Manufacturing Services Carlsbad, CA Drug Product Manufacturing Associate I Bachelor's in an Engineering discipline or Life Science field Exp: 1-2 years |
The purpose of this position is to perform tasks and operations relevant to the bulk formulation and/or filling operations required for sterile production of liquid injectable pharmaceutical products under cGMP regulations in Drug Product Manufacturing. | 07/09/2025 |
| 960 | Argonaut Manufacturing Services Carlsbad, CA Manufacturing Technician II Bachelor's degree in a related field Exp: 1 year |
The Manufacturing Associate II is responsible for executing all manufacturing department processes while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations that could apply. The Manufacturing Associate II is expected to fully participate in both departmental projects and any quality working teams that may be applicable. This position shall be responsible for the hands-on execution of activities as they relate to the manufacturing of products. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. | 07/09/2025 |
| 961 | Argonaut Manufacturing Services Carlsbad, CA Visual Inspection Technician Bachelor's degree in an engineering discipline or life science field Exp: 0-2 years |
The purpose of this position is to participate in tasks related to the visual inspection of manufactured liquid injectable pharmaceutical products under cGMP regulations in Drug Product Manufacturing as well as other types of visual inspection activities, as required. | 07/09/2025 |
| 962 | ARL Bio Pharma Oklahoma City, OK Chemist I - Analytical Bachelor’s degree in chemistry or related science Exp: 1-2 years |
Join a company where you can make a difference from day one and help make the world a better and safer place. ARL Bio Pharma provides analytical and microbiological testing for the pharmaceutical industry. Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug manufacturers, and raw material suppliers bringing excellence to pharmaceutical sciences and making pharmaceuticals safer. This position is a fantastic stepping-stone for those with some basic experience looking to expand their career in the interesting world of the pharmaceutical industry. The Chemist I is responsible for utilizing established methods and standard lab equipment/instrumentation (HPLC, IC) to qualitatively and quantitatively analyze routine pharmaceutical substances and formulations. | 07/09/2025 |
| 963 | ARL Bio Pharma Oklahoma City, OK Chemist I - Chemistry Bachelor’s degree in chemistry or related science Exp: 0-2 years |
This position assists in maintaining the cleanliness of the laboratory, the organization of supplies, reagents and standards. Additionally, this position provides a backup for the daily calibration and/or verification of the balances and pH meter when the Lab Technician is unavailable. The employee will have basic knowledge of commonly used laboratory concepts, practices, procedures and instrumentation and will perform tests commensurate with skill level with some supervision. | 07/09/2025 |
| 964 | ARL Bio Pharma Oklahoma City, OK Microbiologist I Bachelor’s degree in Microbiology or related science Exp: 0-2 years |
Under the supervision of the laboratory supervisor the Microbiologist I provides a high level of quality pharmaceutical microbiology testing as well as effective customer service to ARL Bio Pharma clients. This is a safety sensitive position as defined by state and federal laws that will require working with hazardous materials and/or handling medicine. | 07/09/2025 |
| 965 | VIATRIS St. Albans, VT Chemist SIII Bachelor's degree Exp: 0-2 years |
Every day, we rise to the challenge to make a difference and here’s how the Chemist role will make an impact: Key responsibilities for this role include: Performs and documents the analysis of samples following approved test methods. Calculate, check, and/or review data. Assist with method development, validation, and transfer. Assist with instrument calibrations and maintenance. May work on analytical projects under direct supervision. Attend training classes and seminars as required. | 07/02/2025 |
| 966 | VIATRIS San Antonio, TX Associate Scientist QC Bachelor’s degree in Life Science Exp: 0-2 years |
Every day, we rise to the challenge to make a difference and here’s how the Associate Scientist, QC role will make an impact: Key responsibilities for this role include: Testing of chemical components or products. Will involve the use of major laboratory instruments and equipment: HPLC, GC, FTIR, UV/VIS, as well as utilizing wet chemicals skills. Analytical review of data to ensure calculations is complete and accurate. Performs quantitative chemical analyses of APIs and related materials under direct supervision following established procedures and guidelines using laboratory instrumentation such as gas chromatographs, liquid chromatographs, ultraviolet-visible spectrophotometers, etc. Performs microbiological analysis as required. Treats numerical data throughout chemical analysis by performing mathematical calculations such as determining concentrations (molarity, parts per million, normality, etc.) and statistical information (standard deviation, mean, etc.). Prepares necessary reagents and equipment to expedite the performance of analysis by measuring and/or weighing chemicals, missing, and standardizing solutions, and assembling equipment. Maintains accurate records by logging samples received, recording samples analyzed, procedures used, and results obtained on datasheets and/or laboratory notebook. Weights and calculates samples in the physical and chemical analysis of products using balances and measured volumetric containers. Recognizes and informs Group Leader about daily lab activity and analytical problems. Organizes and properly labels samples, sample preparations, volumetric solutions etc. Maintains area free of sample contamination restores equipment and supplies to designated area; participates in general housekeeping efforts. Must maintain compliance of assigned training plan. Participates in the company performance management program on a regular basis as per the established policy. Within area of responsibility, understand and comply with all DPT safety, environmental and quality practices and procedures as outlined in organizational/departmental guidelines and SOPs as well as applicable federal, state, and local regulations. Perform other duties as assigned. | 07/02/2025 |
| 967 | VIATRIS Morgantown, WV Chemist I Bachelor's degree Exp: 0-2 years |
Every day, we rise to the challenge to make a difference and here’s how the Chemist I role will make an impact: Key responsibilities for this role include: Perform pharmaceutical testing including, but not limited to, HPLC, GC, TLC, UV, dissolution and IR spectroscopy. Demonstrate ability to understand and perform testing in accordance with all pertinent SOPs and lab practices. Critically evaluate and audit data. Write technical analytical reports and procedures. Perform routine testing with a senior level mentor analyst. Perform other duties as assigned. | 07/02/2025 |
| 968 | Vivex Biologics Miami, FL Operations Processing Technician I Bachelor’s Degree in science or related Exp: 0-1 years |
The Operations Processing Technician I support the processing and documentation requirements of tissue during the cleaning, cutting, shaping, inspecting, and packaging operations for transplantation purposes. The Operations Processing Technician I is also responsible for ensuring that all equipment and supplies used for processing are maintained and ready for use, and that all Processing Room maintenance is completed daily while complying with Quality Assurance requirements as mandated by federal, state, and trade regulations. | 07/02/2025 |
| 969 | Waters Corporation Milford, MA Operations Quality Engineer I Bachelor’s degree in engineering, Mathematics, Business, Science Exp: 1-2 years |
Waters Corporation is currently seeking a Quality Engineer to join our organization. This individual is responsible for process quality, data analysis, and for the planning and execution of process improvement projects supporting the Milling department of the Machine Shop within the Milford plant. Responsibilities include leading investigations into product non-conformances, developing and reporting quality system metrics, supporting Statistical Process Control (SPC) initiatives, and driving projects related to product and process quality. This position is hands-on in a fast-paced environment which will interact with multiple functions (Process Engineering, R&D, and other operational departments) as well as additional supporting quality groups to resolve quality issues. | 07/02/2025 |
| 970 | West St. Petersburg, FL Tooling Process Improvement Engineer Bachelor's degree in engineering Exp: 1-3 years |
Support the design and implementation of progressive tooling dies, quality & manufacturing equipment. Contribute to upstream process improvements through use of Lean Six Sigma tools and identify root causes in product rejection. Works as part of a global team and provide technical support to various functional teams. | 07/02/2025 |
| 971 | West Kinston, NC Associate Process Engineer, Sterilization Bachelor’s or Master degree in Biology/ Microbiology /Chemistry or another scientific area Exp: 1-3+ years |
This role is key to developing and introducing process improvements, standards, life cycle management and validation in select process areas, helping to advance and transform West’s growing business, supporting capital investments and contributing to addressing complex assignments. This person has decision rights for his process area, and he/she will have the opportunity to drive the implementation of new innovative processes and technologies in cooperation with the engineering and quality assurance teams and the plants. | 07/02/2025 |
| 972 | HD Biosciences (Wuxi AppTec) San Diego, CA Research Associate II Bachelors in Biology related field Exp: 1-3 years |
Assisting and performing efficacy and PK-PD studies and developing new in vivo/ ex vivo assays and models with minimum supervision, as needed. Help to design, optimize and execute of pharmacology experiments for compound screening, compound mode of action and efficacy in mechanistic and disease models, e.g. syngeneic and xenograft tumor model, acute and chronic autoimmune/inflammatory conditions, and analyses and reporting of experiments or implantation, blood/tissue collection, etc. Assist with and perform other experiments as required. Working with the team to perform assay development, optimization, and validation projects. Following SOPs to perform compound receiving, registration, and management. Help to manage lab coordination | 07/02/2025 |
| 973 | WuXi Biologics Cranbury, NJ Bioprocessing Associate II, MFG DSP Bachelor's Degree or equivalent experience in Science, Engineering or related field Exp: 0-2 years |
Reporting to the Manufacturing Supervisor, Downstream, the Bioprocessing Associate I role will work with the wider Manufacturing teams to support the production of biological products at the MFG18 Cranbury facility. This role will be responsible for procedures and processes associated with the manufacture of Drug Substance. | 07/02/2025 |
| 974 | WuXi Biologics Cranbury, NJ Research Associate Co-op, Downstream Process Development BS or MS in Life Sciences or related field Exp: 0-2 years |
Designs, executes and authors downstream purification development, optimization, scale up and tech transfer. Collaborates with other internal PD teams during process development and tech transfer. Supports pilot production, GMP manufacturing and related investigation studies. | 07/02/2025 |
| 975 | WuXi Biologics Cranbury, NJ Research Associate Co-op, Cell Culture Process Development BS or MS in Life Sciences or related field Exp: 0-2 years |
Designs, executes and authors upstream cell culture development, optimization, scale up and tech transfer. Collaborates with other internal PD teams during process development and tech transfer. Partner with other internal PD teams during process tech transfer. | 07/02/2025 |
| 976 | WuXi Biologics Cranbury, NJ Associate Scientist, Quality Control Environmental Monitoring Bachelor's degree in Chemistry, Microbiology, Biochemistry or equivalent field Exp: 1+ years |
The QC EM Associate scientist/scientist is responsible for the quality and on-time collection of samples, EM (Environmental sampling), Water and Gas system sampling (when required) with raw material sampling to the various testing sections. This role will also ensure QC deliverables to internal departments and external clients are accurate and consistent. Demonstrates strong oral and written communication skills and actively contributes to training, report generation and GMP documentation. | 07/02/2025 |
| 977 | Xeris Biopharma Chicago, IL Scientist I, Analytical Development (Late Stage) M.S. in a nalytical chemistry Exp: 1-3 years |
This position is responsible for the development of analytical and characterization methods for a range of pharmaceutical dosage forms in support of formulation, process, and specification development. The Scientist I, Analytical Development will work with product development scientists (formulation and analytical) seeking to develop various therapeutic drug product formulations incorporating the company’s XeriSol and XeriJect technologies. This role will also support Quality Control and CMC with respect to establishing product specifications, stability programs, material qualification, method validation, method transfer and process validation. | 07/02/2025 |
| 978 | Yokogawa Newnan, GA Manufacturing Engineer BS degree in Engineering or Engineering Technology Exp: 1-5 years |
The function of the Local Manufacturing & Design Engineering group is to expand the Yokogawa product business by leading the implementation of new local products through local manufacturing (LM) and design while facilitating strong communication with our headquarters (YHQ), Product Management (PMG) and affiliates. There are four main product lines which the group supports: Analytical, Controllers/Recorders, Flow and Transmitters. This role is a combination of manufacturing and design engineering. You will be tasked with creation and maintenance of product drawings and BOM’s, developing procedures, maintaining product compliance and supporting the manufacturing lines. Reports to Local Manufacturing & Design Engineering Manager. | 07/02/2025 |
| 979 | 10x Genomics Pleasanton, CA Quality Engineer I Bachelor’s degree or Master’s degree in a scientific or engineering discipline Exp: 1 year |
We are seeking a Quality Engineer I to join our Quality team. This is an entry-level professional position where you will learn to apply professional concepts and company policies to resolve routine issues. As a Quality Engineer I, you will receive detailed instructions on all work and will have the opportunity to develop a foundational understanding of quality processes within the life sciences industry. You will collaborate with your team to solve problems and contribute to the completion of project milestones. Currently ISO 9001 certified, we are actively working towards ISO 13485 certification to further enhance our quality management systems. Individuals applying for this position must be self-starters, strategic thinkers, action driven, thrive in a fast-paced environment, excel at managing multiple priorities, succeed in communicating across the organization and with external partners, and provide immediate contribution. | 07/02/2025 |
| 980 | Abbott Altavista, VA Assistant Chemist - 2nd Shift Bachelor’s degree, science-related Exp: 1 year |
This position works out of our Altavista, VA location in the Abbott Nutrition division. Our Nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow to keeping adult bodies strong and active. Millions of people around the world count on our leading brands – including Similac®, PediaSure®, Pedialyte®, Ensure®, and Glucerna® – to help them get the nutrients they need to live their healthiest lives. | 07/02/2025 |
| 981 | Abbott Temecula, CA Manufacturing Engineer Bachelors Degree Exp: 0-2 years |
Initiates and completes technical activities leading to new or improved products or process, for current programs, next generation programs and to meet strategic goals and objectives of the company. Prepares reports, publishes, and makes presentations to communicate findings. Analyzes and solves problems from basic engineering principles, theories and concepts through to a wide range of complex and advanced problems which require novel and new innovative approaches or a major breakthrough in technology. Understands engineering principles theories, concepts, practices and techniques. Develops knowledge in a field to become a recognized leader or authority in an area of specialization and applies this knowledge in leadership roles in the company. Incorporates business policies and procedures into task completion. Understands the business needs of the company, and has knowledge of the customer needs of our business. Understands the business cycle and foresight of emerging technologies trends. Cultivates internal and external network of resources to complete tasks. Serves has a resource in the selection orientation and training of new engineers and employees. May lead a project team, determining goals and objectives for the projects. Mentors employees by sharing technical expertise and providing feedback and guidance. Interacts cross functionally and with internal and external customers. Serves as a consultant for engineering or scientific interpretations and advice on significant matters. Acts as a spokesperson to customers on business unit current and future capabilities. Cultivates a wide range of internal networks and begins to develop an extensive external network of resources to facilitate completion of tasks. May lead a project team of moderate scope. Provides guidance to less experienced staff. Acts as a mentor to lower level individual contributors. Influence exerted at peer level and occasionally at first levels of management. Plans, organizes, and prioritizes own daily work routine to meet established schedule. Exercises authority and judgment within defined limits to determine appropriate action. Failure to achieve results or erroneous decisions or recommendations may cause delays in program schedules and may result in the allocation of additional resources. | 07/02/2025 |
| 982 | Abbott Columbus, OH Assistant Microbiologist - 3rd shift Science related Bachelor’s Degree Exp: 1 year |
Apply high quality scientific techniques in the microbiological analysis of raw ingredients, in-process production samples, finished product testing and environmental monitoring, to ensure that all products manufactured are fit for use. Be able to work with fellow microbiologist, with a high degree of motivation, attention to important details with clear communication to all team members. This is important due to the high degree of responsibility and working within a small group where each person is relied upon highly. Prioritize tasks to efficiently be completed with the most accurate results, and to communicate clearly and work together in a team environment. Product testing, Environmental testing, Raw ingredient testing. Documentation, Project work, Troubleshooting. Media preparation/general lab work | 07/02/2025 |
| 983 | Abbott Pleasanton, CA Systems Engineer I Bachelor’s Degree in Engineering (Biomedical, Mechanical, Computer, Electrical, or Software), Computer Science, or related discipline Exp: 6 months |
We are recruiting a Systems Engineer I to join our Abbott Heart Failure team in Pleasanton, CA, Burlington, MA or Atlanta, GA where we are focused on helping people with heart failure manage their health to ultimately change and save lives. The engineer will be primarily working on the CardioMEMS HF portfolio, which remotely monitors changes in pulmonary artery (PA) pressure, which is used to prevent worsening heart failure, lower heart failure mortality rates, and improve quality of life for our heart failure patients. Systems engineering defines, designs, tests, and integrates components, disciplines, and products within the CardioMEMS HF System, including implantable sensors, external reader systems used by clinicians and patients, mobile application software, and cloud-based web applications. The System Engineer will help execute tasks during design change projects and development of next generation products, including requirements definition and management, design documentation, and system testing, verification, and validation. | 07/02/2025 |
| 984 | Abbott St. Paul, MN Supplier Quality Engineer Bachelors degree in Engineering or Science Preferred Exp: 1-3 years |
Ability to effectively communicate, facilitate and organize project activities relating to ensuring supplier quality. Develops and manages project schedules to ensure deadlines are met. Serves as the primary Quality contact for suppliers and provides technical assistance to management for suppliers as requested. Works with supplier development engineering to performs on-site annual and critical component supplier audits to ensure compliance with Quality Systems procedures and CSI requirements. Generates audit reports and ensures supplier audit findings are tracked to timely and closure. Provides quality systems input to suppliers such as, but not limited to: statistical process control, gage R&R studies, and capability studies. Resolves supplier quality issues at incoming inspection and the production line. Provides project team leadership and conducts investigations relating to supplier quality issues. Completes non-conforming material reports (NCMR), supplier requests for change (SRC), supplier corrective action requests (SCARs) and monitors follow-up with assigned supplier base. Routinely reports on supplier performance per defined metrics to management and other team members. Represent Quality during audits and interface with FDA, ISO, or any external auditor. | 07/02/2025 |
| 985 | Abbott Temecula, CA Associate Quality Engineer Bachelor's or Master's degree Exp: 0-2+ years |
Our location in Temecula, CA, currently has an onsite opportunity for a Quality Engineer. Abbott Vascular provides innovative, minimally invasive and cost-effective products for treatment of vascular disease. Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents. Provide Process/Quality Engineering support to manufacturing, helping to ensure delivery of highest quality product to the customer. Provide Process/Quality Engineering support to product development teams, helping to ensure development of highest quality new products. | 07/02/2025 |
| 986 | Abbott Casa Grande, AZ Analytical Chemist Science related Bachelor’s Degree Exp: 1 year |
This position is responsible for performing assays in accordance with required methods. Assure test results meet specification limits and that appropriate quality actions are taken to achieve acceptable product status. Enter data into a Laboratory Information Management System (LIMS) as well as any other applicable systems or documented on appropriate forms. Coordinate testing with processing stages and filing or drying requirements to ensure minimum downtime is occurred during processing, filling or drying operations. Set batch yields, optimizations and releasing product to the filling or dryer production departments from the Processing department. Conduct additional finished product testing including; line monitoring, dilution, carryover or any other required finished product testing. Assists with investigations of testing issues as required under any testing policies. Observe all safety rules and regulations. Reports incidents, near misses, and chemical spills in the proper manner to chemist acting as shift lead, front line leader, or manager. Wears all required personal protective equipment, participates in the Environmental Health and Safety Programs, and forwards any opportunities for improvement. | 07/02/2025 |
| 987 | AbbVie Worcester, MA Technician, Manufacturing II BS in Engineering Exp: 0+ years |
Performs functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components and final materials. Uses sophisticated programs (such as LIMS, SAP, automated control systems, etc.) to collect and evaluate operating data, which can be used to conduct on-line adjustments to products, instruments or equipment. Determines and may assist in developing methods and procedures to control or modify the manufacturing process. | 07/02/2025 |
| 988 | AbbVie North Chicago, IL Associate Scientist II, Toxicology Study Coordinator Bachelor’s or Master's Degree Exp: 0-2 years |
The position of Associate Scientist, Toxicology Study Coordinator is in the Preclinical Safety group and will report to a manager in Toxicology. The Associate Toxicologist aides in the planning, conduct and reporting of non-GLP and GLP toxicology studies, acting to support the Study Director and regulatory infrastructure. | 07/02/2025 |
| 989 | AbbVie North Chicago, IL Associate Scientist, Chemistry II Master’s Degree Exp: 0-2 years |
The Process Chemistry group is responsible for inventing and executing the chemical processes and preparing active pharmaceutical ingredients (API) to enable toxicology studies, clinical trials, and drug product development for AbbVie’s pre-clinical and clinical candidates. We create valuable intellectual property through composition of matter, chemical processes, and technology, resulting in the development of safe and cost-effective commercial manufacturing processes. AbbVie Process Chemistry is seeking a highly motivated Automation Engineering Scientist I to conduct chemical process research and development, supporting projects from pre-clinical stages through commercialization. | 07/02/2025 |
| 990 | AbbVie Worcester, MA Associate Scientist, Process Development II Master’s Degree Exp: No exp |
The Bioprocess Development at the AbbVie Bioresearch Center in Worcester, MA is seeking a highly motivated junior Scientist to join the CHO Cell Line Development team. The Scientist will advance AbbVie’s biotherapeutics pipeline through the development and characterization of highly productive CHO cell lines suitable for cGMP protein manufacturing. The selected candidate will have good experience in mammalian cell culture and demonstrate good aseptic technique history, following standard protocol to generate and analyze precise, reliable, and reproducible data in a timely manner. The candidate will also need to demonstrate good communication, presentation, and technical writing skills, team-working spirit, and strong scientific thinking approach in problem solving. The position is based in AbbVie Bioresearch Centre, Worcester, MA. | 07/02/2025 |
| 991 | Abeona Therapeutics Cleveland, OH Inventory Logistics Associate Bachelor’s degree Exp: 1-4 years |
The Inventory Logistics Associate (ILA) assists in serving multiple business units within the Supply Chain Department. ILA’s will serve as the main conduit for shipping and receiving activities at Abeona Therapeutics location in Cleveland, OH. ILA’s will also support the organization and management of inventory ensuring all materials used in the manufacturing suites are processed and released from the Quality Departments. ILA’s will also be paramount in all aspects of Transportation of Drug Products to the qualified treatment centers for the associated Drug Product. | 07/02/2025 |
| 992 | Abeona Therapeutics Cleveland, OH Environmental Monitoring Associate BS in biochemistry, biology, microbiology, molecular biology or other relevant discipline Exp: 1-3 years |
The Quality Control Analyst I performs routine laboratory activities in support of Good Manufacturing Practices (GMP) testing for Quality Control (QC). Performs Environmental Monitoring (EM) and associated activities. Interacts with employees internal and external to Quality Control. | 07/02/2025 |
| 993 | Abeona Therapeutics Cleveland, OH Quality Assurance Specialist, Supplier Quality Bachelor’s degree in related field Exp: 1 year |
The Specialist I, Supplier Quality will perform routine activities associated with manufacturing of cell and gene therapy products at the Abeona Therapeutics Inc. site in Cleveland, OH. This position supports the release of materials in support of cGMP Operations. The Specialist I, Quality Assurance will report to the Supervisor, Quality Assurance or above. | 07/02/2025 |
| 994 | Abeona Therapeutics Cleveland, OH Specialist I, Quality Assurance - Quality Operations Bachelor’s degree in related field Exp: 1 year |
The Specialist I, Quality Assurance performs routine activities associated with manufacturing of cell and gene therapy products at the Abeona Therapeutics Inc. site in Cleveland, OH. This position supports the maintenance of the quality systems in support of a cGMP Operation for production processes relating to batch record review and release from start to end of manufacturing activities, in-process sampling / testing, primary and secondary packaging, label control, and document management ensuring procedural and regulatory compliance throughout the manufacturing process. The Specialist I, Quality Assurance will report to the Supervisor, Quality Assurance or above and will support manufacturing and quality control as the production area Quality Assurance representative. | 07/02/2025 |
| 995 | AstraZeneca Waltham, MA Scientist, Bioscience BS in Biology, Biotechnology or other relevant area Exp: 1-2 years |
The GCB team is critical for delivering these cellular models and developing methods to prepare primary cell lines for projects aligned with our strategic objective of increasing the translatability of the cell models used in research. We are now offering an exciting opportunity for a dedicated and highly motivated individual to join us in the role of Scientist, GCB. | 07/02/2025 |
| 996 | Adare Pharma Solutions Vandalia, OH Chemist I - Day Shift Bachelor’s degree in Chemistry or closely related field Exp: 0-2 years |
The QC Chemist performs moderately complex physical and chemical testing of intermediate and finished products according to written procedures and trains less experienced Chemists as required. Also responsible for testing of cleaning samples for more complex systems and more advanced instrument maintenance. Responsible for timely analytical data reporting based on project timelines. | 07/02/2025 |
| 997 | ADMA Biologics Boca Raton, FL Chemist I Bioanalytics B.S. in Chemistry, Biochemistry, Molecular Biology, or related science discipline. Exp: 0-3 years |
ADMA Biologics is a biopharmaceutical company dedicated to developing superior products for immunodeficient patients at risk of infection. Our commitment to this underserved population drives our innovation and hands-on approach to production and development, setting us apart in the industry. If you're seeking a dynamic, innovative, and growing company in the biopharmaceutical sector that values excellence and integrity, consider joining ADMA Biologics. We currently have an exciting opportunity for a Chemist I Bioanalytics in Boca Raton, FL! This position is responsible for performing quality control testing of raw materials, in-process, and final products, following general instructions on routine work and detailed instructions on new assignments. | 07/02/2025 |
| 998 | ADMA Biologics Boca Raton, FL Laboratory Technician - Automation Bachelor’s degree in related science discipline Exp: 0-2 years |
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We have an exciting opportunity available for a Laboratory Technician - Automation in Boca Raton, FL! The Laboratory Technician - Automation performs automated laboratory testing to support hyperimmune products for ADMA Biologics. This position is responsible for the receipt, testing and on-time delivery of donor testing and maintaining a cGMP compliant laboratory. Maintaining communication with group leader or department manager to support cross-function relationships with plasma centers and ADMA plasma operations. | 07/02/2025 |
| 999 | ADMA Biologics Boca Raton, FL Specialist QA I - Manufacturing Oversight - Night Bachelor's Degree Exp: 1-3 years |
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a QA Specialist I - Manufacturing Oversight - Night in Boca Raton, FL! The QA Specialist I - Manufacturing Oversight - Night performs manufacturing oversight activities to ensure compliance with policies and procedures. Oversight activities include, but are not limited to, real-time manufacturing batch record review, review of manufacturing documentation (logs, charts, etc.), and resolution of issues on the manufacturing floor. | 07/02/2025 |
| 1000 | AGC Biologics Bothell, WA Downstream Manufacturing Associate I BS/BA Exp: 0-2 years |
Manufacturing Associates work in either Upstream or Downstream teams and execute batch records, run, and monitor equipment, monitor production processes, and complete documentation in line with cGMP (current good manufacturing practices) and GDP (good documentation procedures). In their daily tasks, Manufacturing Associates always observe and follow safety procedures and Standard Operating Procedures (SOPs). Additionally, Manufacturing Associates work cross-functionally with QA, MSAT, Facilities, and other key departments to ensure ongoing manufacturing operations are successful, reliable, safe, and compliant. An Associate I assists with basic bioprocess operations in Manufacturing under supervision in compliance with established processes and standards. | 07/02/2025 |
| 1001 | AGC Biologics Bothell, WA Upstream Manufacturing Associate I BS/BA Exp: 0-2 years |
Manufacturing Associates work in either Upstream or Downstream teams and execute batch records, run, and monitor equipment, monitor production processes, and complete documentation in line with cGMP (current good manufacturing practices) and GDP (good documentation procedures). In their daily tasks, Manufacturing Associates always observe and follow safety procedures and Standard Operating Procedures (SOPs). Additionally, Manufacturing Associates work cross-functionally with QA, MSAT, Facilities, and other key departments to ensure ongoing manufacturing operations are successful, reliable, safe, and compliant. An Associate I assists with basic bioprocess operations in Manufacturing under supervision in compliance with established processes and standards. An Associate I assists with basic bioprocess operations in Manufacturing under supervision in compliance with established processes and standards. | 07/02/2025 |
| 1002 | Agilent Cedar Creek, TX Quality Associate Bachelor’s degree Exp: 1+ years |
Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek -- so they can do what they do best: improve the world around us. Agilent is currently hiring a Quality Associate for our Cedar Creek site. | 07/02/2025 |
| 1003 | Agilent Wilmington, DE Electrical Engineer – Manufacturing Bachelor’s or Master’s degree in Electrical Engineering or a related technical discipline Exp: 1+ years |
At Agilent, we deliver trusted answers that advance the world of life sciences. As a Systems Engineer – Manufacturing, you will play a key role in ensuring our electrical systems and manufacturing processes meet the highest standards of quality, safety, and performance. This role is ideal for an engineer eager to collaborate across teams, solve complex problems, and contribute to continuous improvement in a fast-paced production environment. | 07/02/2025 |
| 1004 | Agilent Frederick, CO QC Analyst - 2nd Shift Bachelor’s or master’s Degree Exp: 1+ years |
As a QC Analyst, you will be responsible for conducting routine and non-routine analysis of raw materials, in-process items, and finished formulations according to standard operating procedures. Your role includes performing biochemical and chemical analyses to ensure product stability, compiling data for documentation, calibrating and maintaining lab equipment, and participating in investigations and report preparation. You may also develop testing methods, review data for compliance, revise standard operating procedures, and perform special projects related to analytical and instrument problem-solving. | 07/02/2025 |
| 1005 | Tempus Research Triangle Park, NC Molecular Technologist I-IV BS/BA or MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Responsibilities: Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Perform routine testing, quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform next-generation sequencing, including nucleic acid extraction, DNA/RNA quantification and qualification, NGS library preparation, probe hybridization, probe/library capture, library cleanup and quantification, loading sequencing libraries onto the Illumina Nextseq, HiSeq4000, and Novaseq. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Obtain 12 continuing education hours in the field of oncology or molecular biology. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 06/23/2025 |
| 1006 | Tessera Somerville, MA Research Associate II, Foundry MS in Biology, Chemistry, Biochemistry, Biotechnology or related field Exp: 0-2 years |
You are driven, motivated, and passionate about working at the forefront of RNA technology- contributing to groundbreaking research. You excel in both independent and team environments, possess impeccable attention to detail, and thrive in a fast-paced setting. Candidates without automation experience are still encouraged to apply. Tessera employees are creative and collaborative problem solvers. They have a strong sense of integrity and unwavering commitment to scientific excellence. | 06/23/2025 |
| 1007 | Tessera Somerville, MA Research Associate II/Senior Research Associate, Oligonucleotide Foundry MS in chemistry, biology, or related life sciences Exp: 1+ years |
You are a skilled individual who can operate in a fast-paced environment, troubleshoot instruments, and document operations independently and as part of a team. You will have the opportunity to organize and present results within the group and interface with other teams, so strong communication skills are critical. You enjoy overcoming challenges in collaboration with colleagues. Tessera employees are creative and collaborative problem solvers. They have a strong sense of integrity and unwavering commitment to scientific excellence. | 06/23/2025 |
| 1008 | Thermo Fisher Scientific Greenville, NC Sr Formulation Technician: Control Room & Lyophilizer Bachelor’s Exp: No exp |
The Sr. Formulation Technician will be able to perform tasks with little to no direction. They will provide guidance in the absence of the Lead Formulation Technician. They will be proficient in aseptic filling and manufacturing. This colleague follows written and verbal instructions using cGMP documents and operating equipment when performing the following duties. Shift hours are 6am-6pm on a 2-2-3 rotating schedule. | 06/23/2025 |
| 1009 | Thermo Fisher Scientific Richmond, VA Assistant Scientist Bachelor's degree Exp: 0-1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 06/23/2025 |
| 1010 | Thermo Fisher Scientific Plainville, MA Sr. Formulation Technician NTO Bachelor's Degree in a related field Exp: 1+ years |
Join our team at Thermo Fisher Scientific as an outstanding Sr. Formulation Technician and be a part of a world-class manufacturing environment. You will play a key role in producing detailed drug product injectables by operating advanced equipment and ensuring the highest quality standards. Your technical expertise will drive process optimizations and successful implementations, making a significant impact on our operations. This is a remarkable opportunity to showcase your skills in a collaborative and inclusive atmosphere! | 06/23/2025 |
| 1011 | Thermo Fisher Scientific Chicago, IL Scientist - HPLC, GMP Masters degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar Exp: 0-2 years |
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. | 06/23/2025 |
| 1012 | Thermo Fisher Scientific Richmond, VA Assistant Scientist - 2nd Shift Bachelor's degree Exp: 0-1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 06/23/2025 |
| 1013 | Thermo Fisher Scientific Grand Island, NY QC Technician II Bachelors’ degree in Science related studies Exp: 1-2 years |
Incoming Quality Control Technician II performs wet chemical analyses and inspections on production commodities and raw materials (i.e. salts, sugars, amino acids, vitamins, etc) following established methods and SOPs in accordance to cGMPs. We need a motivated individual with excellent communication and laboratory skills to coordinate and complete planned and detailed activities within a quality system to ensure product, process, system, or equipment quality requirements are met. | 06/23/2025 |
| 1014 | Thermo Fisher Scientific Wilmington, DE Associate Scientist, Formulations Bachelor's degree in Biological Sciences, or other related degree concentration Exp: 1-2 years |
The associate scientist will perform a variety of routine to complex lab activities related to formulation and overall drug product development of large molecule drug products. The role involves designing and executing the experiments, document experimental details, organize the data, and summarize the findings in a technical summary report. The position emphasizes scientific rigor, collaboration with different functions, and effective communication of findings within the organization. | 06/23/2025 |
| 1015 | Transpire Bio Weston, FL Associate Formulation Scientist MS degree in Chemistry, Chemical/Biochemical Engineering, Biochemistry or a related scientific discipline Exp: 1-3 years |
In this role, the Associate Scientist I/II will provide hands-on formulation and process expertise during the development of clinical and commercial formulations for orally inhaled and nasal drug products (OINDPs). Conducts laboratory activities including formulation and manufacturing process development, manufacturing process scale-up and process transfer activities across equipment, manufacturing scales and sites. The individual will design and execute formulation experiments, organize and analyze results with minimal supervision, and communicate data and interpretation to product development team. Contribute towards the development of orally inhaled and nasal drug products (OINDPs) by following regulatory guidelines, industry best practices, US FDA cGMPs, and other relevant guidelines. | 06/23/2025 |
| 1016 | Transpire Bio Weston, FL Associate Scientist I BSc in Chemistry, Pharmacy or related fields Exp: 0-2 years |
Conduct laboratory activities with limited supervision including for example analyzing raw materials, in-process materials and finished pharmaceutical products for quality, safety, purity, strength and identity using applicable methods or manufacturing drug product, following the cGMP, EH&S and other relevant guidelines of Corporate, FDA and other governing bodies. Independently set up and operate lab equipment, prepare reagents, solvents and solutions for analytical and formulation activities. Prepare and maintain accurate records in lab notebooks of all testing performed. Process analytical data on lab equipment such as HPLC/UPLC, enter data in spreadsheets and conduct routine calculations. Support the manufacture of inhalation drug product. Prepare samples for blend uniformity. Perform equipment qualification and calibrations as directed. Execute approved method transfer protocols. Assist in the training of other scientists. Perform other tasks as assigned. Participate in project activities and support project timelines and proactively contribute to meeting the team objectives. Communicates effectively with team members. Establish and maintain effective relationships with team members. Conduct lab work in accordance with SOPs & STPs; follow Corporate safety rules and procedures. Comply with all Corporate guidelines and policies | 06/23/2025 |
| 1017 | Transpire Bio Weston, FL Associate Scientist II MSc in Chemistry, Pharmacy or related fields Exp: 0-2 years |
Conduct laboratory activities with limited supervision including for example analyzing raw materials, in-process materials and finished pharmaceutical products for quality, safety, purity, strength and identity using applicable methods or manufacturing drug product, following the cGMP, EH&S and other relevant guidelines of Corporate, FDA and other governing bodies. Independently set up and operate lab equipment, prepare reagents, solvents and solutions for analytical and formulation activities. Prepare and maintain accurate records in lab notebooks of all testing performed. Process analytical data on lab equipment such as HPLC/UPLC, enter data in spreadsheets and conduct routine calculations. Support the manufacture of inhalation drug product. Prepare samples for blend uniformity. Perform equipment qualification and calibrations as directed. Execute approved method transfer protocols. Assist in the training of other scientists. Perform other tasks as assigned. Participate in project activities and support project timelines and proactively contribute to meeting the team objectives. Communicates effectively with team members. Establish and maintain effective relationships with team members. Conduct lab work in accordance with SOPs & STPs; follow Corporate safety rules and procedures. Comply with all Corporate guidelines and policies | 06/23/2025 |
| 1018 | Transpire Bio Weston, FL Pharmaceutical Manufacturing Process Associate Scientist BS or MS Degree in Chemical/Biochemical Engineering, Chemistry, Biochemistry or a related scientific discipline Exp: BS 1-5 years; MS 0-3 years |
In this role, the Process Associate Scientist I/II will involve developing and optimizing pharmaceutical manufacturing processes, ensuring product quality and consistency, and complying with regulatory requirements on commercial formulations for orally inhaled and nasal drug products (OINDPs). Conducts pilot scale manufacturing activities including formulation and manufacturing process development, manufacturing process scale-up and process transfer activities across equipment, manufacturing scales and sites. The individual will design and execute formulation experiments, organize and analyze results with minimal supervision, and communicate data and interpretation to product development team. Contribute towards the development of orally inhaled and nasal drug products (OINDPs) by following regulatory guidelines, industry best practices, US FDA cGMPs, and other relevant guidelines. | 06/23/2025 |
| 1019 | Twist Bioscience South SF, CA Manufacturing Associate I, NGS Probe Production Bachelors degree in biology, chemistry, biochemistry Exp: 0-1 years |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations Team in South San Francisco. The Manufacturing Associate, NGS TE will perform basic molecular biology workflows in a highly automated, high-throughput manner and will be responsible for the manufacture of variety of custom oligonucleotide products. The ideal candidate will be able to work independently, be very neat and organized, have the ability to follow established SOPs and complete manufacturing batch records to contribute to the daily production schedule. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast paced start-up environment. The Manufacturing Associate will be responsible for the production of custom gene based products and/or various intermediates according to established SOPs and complete manufacturing batch records to contribute to the daily production schedule. They will uphold standards as defined by the manufacturing process, work on continuous improvement and have good time management resulting in efficiency, and work in a safe manner. | 06/23/2025 |
| 1020 | Twist Bioscience Portland, OR Automation Service Engineer BS in Engineering (Mechanical, Electrical/Electronics) or Biological Science field or related technical discipline Exp: 1-2 years |
The Engineering group at Twist is a team of diverse backgrounds (engineers, biologists and chemists) who have a huge and direct impact on Twist products. Our team designs and develops several new engineering solutions that are used in development and production and are critical to synthesis of oligos and DNA. As an Automation Service Engineer, you will own the support of scalable and robust solutions for custom oligo and gene products. These solutions will be an interesting combination of hardware, software and biological systems. The focus will be on liquid handling, mechanical design and data analytics. | 06/23/2025 |
| 1021 | Ultima Genomics Fremont, CA Product Engineer I BS or MS in Engineering or core scientific degree Exp: 1+ years |
We are looking for a highly motivated Product Engineer I to join our team! Our Product Engineer plays a strategically important role in ensuring the company’s business success. The primary responsibilities include, but are not limited to, supporting Field Service Engineers (FSEs) and Field Application Scientists (FASs) groups with technical support, authoring and reviewing Best Known Practices (BKPs) for field deployment, and coordinating the rollout and implementation of Engineering Change Orders (ECOs) in the field. In this Product Engineer (PE) position, you will train FSE’s on best practices and be the point of contact for field escalations. PEs are system experts and sometimes work side by side with R&D to gain a deep understanding of the system. PEs will help define problem statements, develop mitigations, and are a key contributor to Corrective Action Preventative Action (CAPA) plans. | 06/23/2025 |
| 1022 | United Therapeutics Manchester, NH Research Associate II - Tissue Engineering Master’s degree in a Biotechnology, Biomedical Engineering, or Cellular Biology field Exp: 1 year |
Execute laboratory cellular research tasks related to organ scaffold 3D printing; support the company’s goal of establishing new experimental procedures and analytical metrics to characterize the biological outcomes of different lung cell types on 3D printed lung scaffolds. Perform cell studies experiments to address the technical challenges with efficient post-processing of 3D printed objects. Implement biochemical assays to evaluate cell phenotypes after cellularization of 3D printed scaffolds, including imaging (bright field, confocal, lightsheet), immunostaining, and qPCR. Implement and evaluate culture methods using bioreactor systems. Perform biochemical assays following manufacturer instructions. Record and manage the use of the materials and reagents needed to carry out experiments. Record all laboratory data in the in-house data management systems. Prepare reports, technical documents and Standard Operating Procedures for internal and external use. Apply effective communication and data organization skills to report and present scientific data to other team members individually and at group meetings. Apply knowledge biological/biomedical/biotechnology concepts, standards and methods to execute 3D printing, scaffold processing, and bioreactor assembly for cellularization experiments. | 06/23/2025 |
| 1023 | United Therapeutics Research Triangle Park, NC Bioprocess Technician - Tissue Engineering Development Bachelor’s Degree in life science, engineering, or biomedical science Exp: 1+ years |
If you're passionate about advancing research for the treatment of pulmonary hypertension and other lung diseases, this role is for you! As part of our innovative research team, you’ll play a pivotal role in developing regenerative medicine products by operating lung recellularization systems and supporting tissue engineering processes. You’ll assist in preparing human and non-human tissues, performing assays, maintaining bioreactors, and analyzing data—contributing directly to the development of groundbreaking treatments. If you thrive in a collaborative, hands-on lab environment and are eager to apply your technical skills to real-world medical solutions, this position offers a unique opportunity to make a meaningful impact. | 06/23/2025 |
| 1024 | United Therapeutics Manchester, NH Associate Print Process Engineer Bachelor's degree in mechanical, chemical or biomedical engineering, or related field Exp: 1+ years |
We are looking for our “jack of all trades” to work on the worlds most advanced 3d printing technology printing the worlds most advanced 3d printed object ever – a human lung. If you want to take your SLA/DLP 3D printing experience to the next level and learn under a team of experience print engineers who love to teach and mentor, apply below. The Associate Print Process Engineer is responsible for systems development projects to build cutting edge 3D printers for lung scaffold printing. This work will support the development of methods to produce 3D printed lung scaffolds that are suitable for cellularization and will include both in-house development and coordinating with external partners to meet project milestones. | 06/23/2025 |
| 1025 | United Therapeutics Eden Prairie, MN Preclinical Research Associate I Bachelor’s Degree in biology, biomedical, or other related health fields Exp: 1+ years |
We are looking for our motivated, self starting human with a service mentality. This person will have experience with animals in a research setting and have an eye for details and data while being eager to learn all they can and make an impact. This is a once on a lifetime opportunity to take your preclinical experience and apply it to a product like transplantable kidneys or livers. Sound like something you want to be apart of? Apply below. The Preclinical Research Team works with small and large, cross-functional teams on our early and late-stage development projects to advance Miromatrix programs. The Preclinical Research Associate I will work with the Preclinical Team to support the planning and conducting of pre-clinical experiments, analyzing data, and documenting results that enable teams to make decisions and progress the programs towards the clinic. This position will attend procedures at regional contract research organization and universities to assist with data collection and study duties that support the goals of the preclinical program. | 06/23/2025 |
| 1026 | United Therapeutics Manchester, NH Print Process Engineer Masters Degree in mechanical, chemical or biomedical engineering, or related field Exp: 1 year |
We are looking for our “jack of all trades” to work on the worlds most advanced 3d printing technology printing the worlds most advanced 3d printed object ever – a human lung. This position is multi faceted and works at the center of different groups, technologies and hardware. Interested? Apply below! The Print Process Engineer is responsible for systems development projects to build cutting edge 3D printers for lung scaffold printing. This work will support the development of methods to produce 3D printed lung scaffolds that are suitable for cellularization and will include both in-house development and coordinating with external partners to meet project milestones. | 06/23/2025 |
| 1027 | Unither Manufacturing Rochester, NY QC Chemist Associate B.S. in chemistry or related science discipline Exp: 0+ years |
Performs routine analyses of materials, drug substances and drug products following cGMPs. May support analytical method development & validation, and analytical troubleshooting under technical supervision. Assists with maintaining lab quality systems. | 06/23/2025 |
| 1028 | Unither Manufacturing Rochester, NY Validation Technician BS Exp: No exp |
Assists validation efforts in many ways including the following: executes/supports equipment, cleaning, and process qualifications, takes and delivers samples, collects and compiles data for validation reports, assists in maintaining of the Validation Document Library, maintains test equipment and documentation system. | 06/23/2025 |
| 1029 | Valo Health New York, NY Engineer I, Tissue Engineering Bachelor’s degree in mechanical, electrical or biomedical engineering Exp: 1+ years |
As a Tissue Engineer I within the Translational Biology department, you will be part of a team of data scientists, translational biologists, and engineers building a powerful computational platform for advancing the research and development of new medicines. You will work on the BiowireTM platform, which generates biofidelic engineered human cardiac and skeletal muscle tissues. BiowireTM is a cornerstone of the larger Opal Computational PlatformTM which evaluates the safety and efficacy of drugs in various models at a decreased cost as compared to human trials, and ethically as compared to animal testing. Successful candidates will work with a diverse set of scientists and engineers in ways that cut across traditional industry boundaries. | 06/23/2025 |
| 1030 | Vantage MedTech Lenexa, KS NPI Engineer BS or MS degree in Engineering, preferably Mechanical or Manufacturing Engineering. Exp: 1-3 years |
The NPI (New Product Introduction) Engineer will be responsible for ensuring that our innovative designs are transitioned into effective and sustainable production. Our life saving products are manufactured in Kansas City and require predictable delivery of high quality, cost-effective production over 5+ year product lifetimes. You will collaborate with Vantage MedTech’s Engineering and Manufacturing teams to provide input on the device design’s manufacturability, and plan and execute the transfer of these new products to our manufacturing facility. You will be responsible for ensuring that robust manufacturing processes are created, updated and in compliance with company standards, ISO, and GMP as required. In addition, you will help drive improvement projects that impact quality and productivity. | 06/23/2025 |
| 1031 | Vector Laboratories Newark, CA Manufacturing Associate I, NGS Probe Production BS or BA degree in Chemistry Exp: 0-3 years |
The Manufacturing Associate I is primarily responsible for manufacturing Vector’s products according to established procedures and documenting all work in production batch records using established good documentation practices. The Manufacturing Associate I will operate and maintain common laboratory equipment as per instructions and works under general supervision on assigned tasks. Technical expertise should include strong knowledge of general laboratory safety and practices, basic knowledge of modern synthetic organic chemistry, multistep synthesis, and purification technique. This position will report to the Site Leader. | 06/23/2025 |
| 1032 | Phillips Medisize Costa Mesa, CA Quality Engineer Bachelor's Degree in an Engineering Field Exp: 1+ years |
Use quality tools to implement improvements including: process flowcharting, Pareto analysis, correlation and regression analysis, significance tests, design of experiments, statistical process control, gauge repeatability and reproducibility, and trend analysis techniques. Assist the development of essential QMS deliverables/Advanced Product Quality Planning (APQP) including, but not limited to: complaint analysis, risk analysis, failure mode and effects analysis, CAPA, and process/equipment/software verification / validation. Monitor production processes and products for adherence to company and regulatory standards and practices. Participate in quality improvement initiatives and projects. Perform quality reviews and internal audits; evaluate data and write reports to validate or indicate deviations from existing standards. Review and approve change requests. Manage the qualification of processes performed by suppliers; troubleshoot and lead corrective actions relating to supplier performance; improve process for supplier data submission to reduce internal inspections. Facilitate communication between engineering, manufacturing, and quality functions. Responsible for being a communication liaison between the customer and manufacturing facility. | 06/23/2025 |
| 1033 | Phillips-Medisize Hudson, WI Validation Engineer Bachelor’s Degree in a scientific discipline Exp: 1+ years |
Coordinate and lead validation projects and discussions. Work with project teams to define the validation strategy. Draft MVPs, equipment qualification, protocol/test case, deviations and summary report documentation for project wrap up. Execute computer system/software validation activities including risk assessments and part 11 compliance requirements. Interface with customers to resolve issues and harmonize validation requirements. Learn and deploy SAP related tools and deliverables associated with validation documents and document approval workflows. Provide statistical analysis support to sites and validation teams. Assist with creating, updating, and training on WI, SOP, and other necessary documents needed to perform validation work. Support global rollout of Global Validation requirements and on-site or desk audits of Phillips-Medisize sites to ensure compliance to the global standards. Share validation best practices information and suggest improvement opportunities. Travel to other Wisconsin Phillips Medisize sites (up to 50%) with occasional travel outside Wisconsin as needed. | 06/23/2025 |
| 1034 | Velocity Clinical Research Durham, NC Clinical Research Coordinator I Bachelor’s degree Exp: 1 year |
The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs. | 06/23/2025 |
| 1035 | Veloxity Peoria, IL Associate Scientist II Bachelor’s degree in science (chemistry/biochemistry preferred) Exp: 1-2 years |
As an Associate Scientist II, you will be using state-of-the art technologies to perform bioanalytical testing for emerging pharmaceutical and biopharma companies. At Veloxity, we hire driven and motivated individuals and provide training and career advancement opportunities within our organization. | 06/23/2025 |
| 1036 | Veracyte Austin, TX Specimen Processor Bachelor’s degree Exp: 0-2 years |
The Specimen Processor in this CLIA Laboratory is a critical member of the laboratory team, responsible for receiving, accessioning, and documenting specimens with precision. This role requires accurate data entry, proactive identification, and resolution of sample integrity issues. Flexibility in scheduling, including holidays and variable shifts, is essential to meet operational demands. | 06/23/2025 |
| 1037 | Vertex Pharmaceuticals San Diego, CA Protein Sciences Senior Research Associate Masters Degree in biological sciences Exp: 0-2 years |
Vertex Pharmaceuticals is seeking a highly motivated Senior Research Associate to join the Protein Sciences team in San Diego. The Protein Sciences team is responsible for guiding our drug discovery programs through key molecular insights that underlie disease target function and modulation. The successful candidate will support the advancement of our research programs to create transformative medicines for patients with serious diseases through the generation of high-quality recombinant proteins for biochemical, biophysical and / or structural biology experiments. | 06/23/2025 |
| 1038 | Alora Pharmaceuticals Forth Worth, TX QC Chemist I BA/BS in Chem Exp: 0 years |
The primary function of a QC Chemist is to perform qualitative and quantitative chemical and physical analysis in support of raw materials, in-process samples, components, and finished drug products testing. | 06/23/2025 |
| 1039 | Alora Pharmaceuticals Forth Worth, TX QC Chemist II BA/BS Chemistry Exp: 1 year |
A Chemist II completes testing independently. May perform non-routine method transfer and instrument troubleshooting with supervision if required. A Chemist II has good oral and written communication skills. A Chemist II has strong lab-work skills and good understanding of chemical testing equipment and processes. A Chemist II has a good understanding of cGMP, DEA regulations, and Quality Procedures for working in a QC Lab. A Chemist II knows the basic concepts of statistical treatment of experimental data. Proposes conclusion congruent with experimental results. A Chemist II can identify routine technical problems and seeks help to solve them. Knows basic skills for OOS, OOT, and aberrant result investigations. A Chemist II has proficient level of understanding of lab instruments and equipment knowledge and basic trouble shooting skills. | 06/23/2025 |
| 1040 | Alora Pharmaceuticals Marietta, GA Process & Product Development Scientist - Osmotica Bachelor's or Masters degree in chemistry, engineering, pharmacy or a related scientific discipline. Exp: 0-3 years |
The incumbent is responsible for supporting Technology Transfer and Product Development of pharmaceutical dosage forms and drug delivery systems for new and existing chemical entities according to approved plans/protocols. The Process and Development Scientist is responsible for developing, organizing, and leading development activities in the manufacturing area and performing developmental activities. The Process and Development Scientist also performs related technical writing functions, including Standard Operating Procedures (SOPs). The incumbent is also responsible for operating the laboratory process and testing related equipment in the Pharmaceutical Sciences Laboratory. | 06/23/2025 |
| 1041 | VGXI Conroe, The Woodlands, TX Environmental Monitoring Technician Bachelor’s degree Exp: 1-3 years |
The primary responsibility of Environmental Monitoring Technician is to perform all EM monitoring and related testing, water sampling and testing. Responsibilities also could include in-process and release testing of products manufactured at VGXI. Set-up, organization, and day-to-day operations of a Quality Control Lab are also required. | 06/23/2025 |
| 1042 | VGXI Conroe, The Woodlands, TX Upstream & Downstream Manufacturing Process Technicians Bachelor’s degree Exp: 1-3 years |
Responsible for manufacturing revolutionary clinical and commercial nucleic acid-based pharmaceuticals by interfacing with manual and automated production systems and controls in cGMP manufacturing environment while maintaining areas in a state of compliance with internal quality systems. Follows standard operating procedures to operate production equipment for upstream/downstream operations. Maintains records, process, and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for proficiency in assigned functional area: Upstream/Downstream Manufacturing. Understands and applies biological, chemical, and mechanical principles and techniques. | 06/23/2025 |
| 1043 | PerkinElmer Annapolis, MD CCFS Media Prep Technician Bachelor Degree in a chemistry, biology, or other relevant discipline Exp: 0-1 years |
Work with Cell Culture and Fermentation Suite scientists to prepare cell culture media, feed, stocks, buffers and reagents. Primary duties will include preparing many types of biological cell culture basal media, nutrient feed and stock solutions for NS0, CHO and hybridoma cells. Solutions will be tested for osmolarity, pH, and turbidity. Using aseptic technique and a biological safety cabinet, filter or pump solution into sterile containers as requested by scientists and store all solutions properly. Lab instrument maintenance for Nova, Cedex, BGA, pH meter and osmometer as schedule permits. Monitor stock solution inventory and prepare as needed. Label all solutions according to CCFS guidelines. Work with scientists to prepare custom solutions and make modifications as needed to standard media and feed formulations. Update the Solution Preparation Console daily to reflect all lot numbers, catalog numbers and formulation modifications as well as storage conditions. Calibrate laboratory equipment as required. Clean and sterilize BSC according to schedule. Monitor inventory in cold room and feed cabinet, discarding expired solutions and maintaining stock of general use solutions. Maintain inventory of all chemicals in the cold room and media prep laboratory. Receive chemicals, barcode, and log into the Chemical Inventory Console. Retire chemicals from the inventory console as needed. Provide support with the design of small bioreactor performance of experiments on media stability. Assist in the preparation of laboratory SOPs. Maintain work environment to guarantee the success of aseptic operations. Record and keep accurate material inventory and update database. Keep laboratory notebooks up to date. Communicate effectively with internal customers. Maintain training and compliance in areas of health and safety, security, environmental and operational aspects of daily activities in the working environment. May require support of on-call service for specific research units in the lab areas. Hours are between 5:00pm-7:30am Monday thru Sunday. Tasks include but are not limited to transfer of contents from failing fridges and incubators to designated back up units, photograph original items, properly document failure, provide a work order of failing unit to facilities team and inform respective end-users about the transfer via email based on the SOP instructions. | 06/23/2025 |
| 1044 | Viant Laconia, NH Quality Engineer Bachelor’s Degree in Engineering or related field Exp: 0-2 years |
The primary purpose of this role is to support Operations by ensuring adherence to Quality System requirements for medical device manufacturing/operations in accordance with applicable Regulatory and Standards requirements for compliance. | 06/23/2025 |
| 1045 | scPharmaceuticals Burlington, MA Quality Associate Bachelor’s Degree Exp: 1+ years |
The role of The Quality Associate will support the company’s quality and regulatory systems in compliance with industry best practices. They will primarily support the Product Complaint Handling process. This position reports to the Quality Director. | 06/18/2025 |
| 1046 | Pfizer McPherson, KS EHS Senior Associate Master's degree Exp: 0 years |
The successful candidate will be part of a dynamic team of experts who form Pfizer’s Environment, Health, & Safety division. Due to the importance of this team for Pfizer’s employees and patients, the organization relies heavily on its team members’ timely actions and efficiency. You will be responsible for activities involved in identifying hazardous workplace conditions and take effective steps to ensure that workplace conditions comply with applicable federal and state Occupational Safety and Health standard provisions. You will assist in the development and implementation of short- and long-range plans and continuously improve EHS performance. As a Senior Associate, your ability to meet team targets will help in completing important deliverables on time. Your innovative use of communication tools and techniques will make it easy to manage difficult issues and help in establishing consensus between teams. It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe. | 06/18/2025 |
| 1047 | Pfizer Sanford, NC QC Scientist Method Transfer and Validation Master's degree Exp: 0+ years |
You should be able to review the validation data as a second analyst reviewer. Ensures that quality control procedures adequately evaluate an organization's products. Determines if current methods and techniques result in meeting reliability standards or require modification. (More concerned with standards, methods and procedures than with testing devices and equipment used to check products). Devises testing plans, methods and equipment to assure reliability of product in conjunction with product design and specifications. (More concerned with tests and quality control checks during and after product preparation.) Tests and inspects products to determine compliance with specifications. Include on- and off-line inspection. Performs laboratory tests on finished products, raw materials, and in-process material in support of the company's quality control program. Prepares reports and/or exercises administrative control in support of the company's quality control program. | 06/18/2025 |
| 1048 | Pfizer Sanford, NC QC Senior Associate Scientist - Method Transfer and Validation Master's degree Exp: 0+ years |
The resource will work on-site at the Pfizer, Sanford, North Carolina facility and will be a member of Pfizer’s Quality Control Portfolio Management team to support multiple quality programs. You will be able to perform chemical, or biological or microbiological analysis on products. The colleague should be able to perform the analytical or chemical or microbial and sterility testing in the GMP laboratory setting and should be able to collaborate efficiently with the external teams. Additionally, the candidate should be able to document all the data to in accordance with cGMP and data integrity principles. | 06/18/2025 |
| 1049 | Pfizer Rocky Mount, NC QC Lab Analyst II Bachelor’s degree Exp: 0+ years |
The QC Chemistry Lab Analyst IIwill perform basic analysis for raw materials, in process and finished products a safe, compliant, and efficient manner. The Job responsibilities include performing wet chemistry and analytical testing to evaluate the quality of the incoming raw materials and analyze the finished product to demonstrate that the quality of our products meet the high standards of quality. Report testing results through computerized systems, or through standard laboratory paper-based documentation. Other related duties essential to these operations or special assignments as required. | 06/18/2025 |
| 1050 | Pfizer Rocky Mount, NC QC Chemistry Lab Analyst II Bachelor’s degree Exp: 0+ years |
The CQ Lab Analyst II, will perform basic analysis for Validation of new and existing products on manufacturing lines in a safe, compliant, and efficient manner. The Job responsibilities include performing wet chemistry and analytical testing to evaluate the quality of multiple sample sites across the manufacturing process to demonstrate that our process is able to meet the high standards of quality for patient use. Report testing results through computerized systems, or through standard laboratory paper-based documentation. Other related duties essential to these operations or special assignments as required. | 06/18/2025 |
| 1051 | Pfizer Rocky Mount, NC QC Senior Scientist Master's degree Exp: 0+ years |
QC Senior Scientist will be recognized as a technical expert and a scientific contributor. With the deep knowledge of the discipline, QC Sr. Scientist will be an active team member whose decisions impact the project. QC Sr. Scientist will be using scientific judgment to adapt standard methods and techniques by applying prior work experience. QC Sr. Scientist will be forecasting and planning resource requirements for project team. QC Sr. Scientist creativity in developing novel processes and new ideas will be used frequently. QC Sr. Scientist will undertake mentoring activities to guide team members. | 06/18/2025 |
| 1052 | Pfizer Pearl River, NY Sr Associate Scientist - Conjugation MS degree in Chemistry/Organic Chemistry or related discipline Exp: 0-4 years |
As a Senior Associate Scientist in the Early Bioprocess Development within Pfizer Vaccine Research and Development, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will join a large team of Scientists focused on conjugation process development for manufacturing carbohydrate-based conjugate vaccines. Primary duties include supporting the development and optimization of conjugation methods, purification, and analysis of intermediates and glycoconjugates using chemical and chromatographic methods. The individual will become a key contributor towards supporting the early development and scale up of glycoconjugate vaccines. Careful documentation of work and presentation of data is required. All work is to be done in a compliant manner according to SOP guidelines and cGMP/GLP regulations, where applicable. | 06/18/2025 |
| 1053 | Sequel Med Tech Manchester, NH Postmarket Quality Engineer Bachelor's degree in a technical field Exp: 1+ years |
The Quality Engineer will be a key member of our growing Post Market Surveillance team as we build our Quality Management System. The Quality Engineer will primarily support post market surveillance processes, but may provide support across the QMS, including maintaining and improving Quality Management System processes, supporting corrective and preventive actions, quality engineering support for complaint investigations, and field actions, as needed. This is an office-based position in Manchester, NH. | 06/18/2025 |
| 1054 | Sequel Med Tech Manchester, NH Quality Engineer Bachelor's degree in a technical field Exp: 1+ years |
The Quality Engineer will be a key member of our growing Quality/Regulatory team as we build our Quality Management System. The Quality Engineer will provide support across the QMS which may include responsibility for maintaining and improving the Quality Management System processes, control of documents and training materials, and quality engineering support for product development, and supplier management. This is an office-based position in Manchester, NH. | 06/18/2025 |
| 1055 | Siegfried Irvine, CA Quality Assurance Associate II BS degree in Biochemistry, Chemistry, Engineering, Biology or closely related Exp: 1-2 years |
This position supports the Quality Assurance Operation, which consists of QA shop floor supports, and QA batch review and Product Release. | 06/18/2025 |
| 1056 | Boston Scientific Quincy, IL Quality Engineer I Bachelor's Degree in engineering related field Exp: 6+ months |
The Quality Engineer I will utilize quality-engineering methodologies, systems, and practices to directly support the inbound and outbound distribution of Boston Scientific Cardiac Rhythm Management (CRM) and Neuromodulation (NMD) products within the Quincy, MA distribution center. This engineer will play a key role in ensuring the day-to-day supply chain executes successfully – supplying medical devices real time to BSC customers around the world. | 06/18/2025 |
| 1057 | Singota Solutions Bloomington, IN Quality Associate 1 - Quality Events Bachelor’s Degree – Science related field Exp: 1-3 years |
The Quality Associate 1- Quality Events position is responsible for supporting and maintaining the GMP-compliant quality systems related to deviations and CAPAs (Corrective Action & Preventative Action). This role provides quality oversight of quality event lifecycle management, ensures adherence to internal procedures and regulatory requirements, and interfaces directly with internal teams, external clients, and regulatory bodies. This position plays a key role in maintaining site compliance and driving continuous improvement across operations. | 06/18/2025 |
| 1058 | Revvity Remote, NJ Field Service Engineer BS/BA in a STEM field Exp: 0-2+ years |
Revvity is seeking a qualified candidate to join the Service Team in our Life Sciences & Diagnostics Business Unit. The individual will be responsible for supporting several testing labs in the greater New York City and New Jersey area. | 06/18/2025 |
| 1059 | SMC, Ltd Concord, NC Quality Control Technician Bachelor’s degree in Microbiology, Chemistry, Biochemistry, or a related field Exp: 1-2 years |
The Quality Control (QC) Technician is an entry level position that supports daily operations of the Quality Control department within the pharmaceutical manufacturing environment. This role involves routine activities that contribute to maintaining product quality and compliance. The ideal candidate is detail-oriented, dependable, and comfortable working in a regulated setting. Flexibility with scheduling, including early or late shifts and occasional weekend work, is required. | 06/18/2025 |
| 1060 | Smithers Gaithersburg, MD Scientist MS in biology, life sciences, or chemistry field Exp: 1 year |
Smithers PDS is seeking a Scientist to join our team in Gaithersburg, MD. The Scientist performs data analysis and various assays according to SOP with reliability while applying and meeting GLP, GCP, and/or CLIA requirements. This position assists with ensuring that the lab, materials, and equipment are maintained. | 06/18/2025 |
| 1061 | Smithers Columbus, OH Associate Microbiologist B.S. degree in microbiology or related field Exp: 6 months |
The Associate Microbiologist will conduct microbiological analysis of cannabis flower, concentrates and infused products as required by the state cannabis regulatory body regulations within an ISO 17025 accredited laboratory. The Associate Microbiologist will be responsible for coordinating scheduling with the Laboratory Manager, conducting sample analysis, and entering sample information into the laboratory information management system (LIMS). As time allows, the Associate Microbiologist will also be cross-trained to conduct sample preparation and extraction for subsequent chemical analyses. | 06/18/2025 |
| 1062 | Sonothera South SF, CA Research Associate/Sr. Research Associate, Histology Bachelor’s degree in Biology, Neuroscience, or related field Exp: 0-3 years |
The Gene Therapy group at SonoThera is seeking to hire a Research Associate/Senior Research Associate to become an integral part of the gene therapy drug development effort. We seek candidates who think critically and have the desire and ability to learn new techniques. This position requires adaptability and an ability to perform at a high level in a fast-paced environment. A qualified candidate will have broad technical experience in sample processing for histology. | 06/18/2025 |
| 1063 | Standard BioTools Boulder, CO Research Associate I BS or MS in molecular biology, biochemistry, chemistry or related field Exp: 1-3 years |
As part of the Assay R&D team, RA I will contribute to both new product development at all phases and sustaining activities related to existing products. New product development activities will be primarily related to SomaScan products (e.g., new assay formats, expanded content, alternative readouts). Additional tasks related to other SBI product lines including KREX or microfluidic applications will also fall within the scope of the RAI’s role. They will be involved in troubleshooting activities related to assay or instrumentation failures and perform tasks related to maintaining existing product lines. A successful candidate will have strong laboratory bench skills, particularly when executing biochemical laboratory techniques. The ideal candidate will additionally have proven experience designing and executing complex experiments in an R&D environment. | 06/18/2025 |
| 1064 | Starkey Eden Prairie, MN Regulatory Affairs Specialist I BS or MS in Science or Engineering Exp: 1-2 years |
This position is responsible for supporting the Regulatory Affairs Department for all medical devices and hearing related products. This position will work with various departments across the organization with focus on new product development. The Regulatory Affairs Specialist is responsible for supporting activities that keeps Starkey current with changes to medical device regulation and for creating and maintaining the technical files for all medical devices and hearing related products. | 06/18/2025 |
| 1065 | STERIS Coon Rapids, MN Quality Analyst Bachelors degree (Scientific or related technical field) Exp: 1 year |
The Quality Analyst in the STERIS Applied Sterilization Technologies (AST) Coon Rapids, Minnesota facility is responsible for assisting in administration of the quality management system at a site to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. The Quality Analyst leads complaint/CAPA investigations, supplier quality improvement initiatives, continuous improvement initiatives and countermeasures with the use of statistical techniques and other accepted quality principles. The Quality Analyst executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. The Analyst also supports production and quality operations by coordinating and performing problem-solving investigations, pre-reviews and final acceptance/run release of processing runs that contain non-conformances. | 06/18/2025 |
| 1066 | STERIS Montgomery, AL Quality Engineer Bachelor’s Degree in Engineering or related technical field Exp: 1 year |
The Quality Engineer in our Montgomery AL location is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. The Quality Engineer supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 06/18/2025 |
| 1067 | STERIS St. Louis, MO Quality Engineer BS Chemical, Biochemical or Biomolecular Chemical Engineering. Exp: 1 year |
The Quality Engineer in our St. Louis, Missouri facility is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. As a Quality Engineer, you will support complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 06/18/2025 |
| 1068 | STERIS Conoroe, TX Quality Engineer Bachelor’s Degree Engineering or related technical field Exp: 1+ years |
The Quality Engineer in our Conroe, Texas facility is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. As a Quality Engineer, you will support complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 06/18/2025 |
| 1069 | STERIS Mentor, OH Quality Analyst Bachelors degree (Scientific or related technical field) Exp: 1 year |
The Quality Analyst in our STERIS Applied Sterilization Technologies (AST) Mentor, OH facility is responsible for assisting in administration of the quality management system at a site to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. The Quality Analyst leads complaint/CAPA investigations, supplier quality improvement initiatives, continuous improvement initiatives and countermeasures with the use of statistical techniques and other accepted quality principles. The Quality Analyst executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. The Analyst also supports production and quality operations by coordinating and performing problem-solving investigations, pre-reviews and final acceptance/run release of processing runs that contain non-conformances. | 06/18/2025 |
| 1070 | STERIS Liberetyville, IL Scientist I B.S. degree in a technical discipline Exp: 1-3 years |
This Scientist I is responsible for the activities related to validation of sterilization processes across STERIS operating facilities. Activities include calibration of data collection systems, such as maintaining dosimeters and dosimetry equipment, measurement of dosimeters for report generation; operation, and data collection related to portable temperature/humidity sensors; coordinating with external laboratories for equipment calibrations and maintenance; coordinating with Customers for test sample processing and requalification studies; coordination and proper handling of product samples for transfer to outside laboratories for testing; and other routine tasks as directed by the immediate supervisor or manager. | 06/18/2025 |
| 1071 | Sterling Germantown, WI Analytical Chemist Bachelors Degree in Chemistry or related field Exp: 0-2 years |
As the Analytical Chemist at Sterling, you will be accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of active pharmaceutical ingredients development or pharmaceutical manufacturing. Testing performed directly supports manufacturing through the release of raw materials, intermediates and API’s; as well as in-process controls, equipment cleaning verification, reference standard qualification, and stability program. The Analytical Chemist will develop the ability to efficiently organize the routine work with minimum supervision and to properly evaluate and interpret generated data working. | 06/18/2025 |
| 1072 | Strand Therapeutics Boston, MA Associate Scientist, Analytical Operations M.S. in Chemical Engineering, Bioengineering or similar Exp: 1-2 years |
Strand is looking for people who have the enthusiasm and motivation to be a highly contributing member of a small but extremely productive team. This opportunity will offer the employee the ability to work in a matrix-based environment and be a part of the future strategy of the company. We are looking for a highly motivated and innovative candidate for the role of Associate Scientist of Analytical Operations. This individual will support in day-to-day analytical operations as an analyst. Reporting initially to the Senior Scientist of Analytical Development, the right candidate will be a strategic thinker that brings a leadership presence and enthusiasm for Strand along with a deep scientific knowledge. | 06/18/2025 |
| 1073 | Stryker Portage, MI Electrical Engineer, R&D Sustainment Bachelor's degree in Electrical Engineering Exp: 0+ years |
This Electrical Engineer role will support sustainment projects, working with other product engineers, R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management to ensure project success. With coaching and mentorship, you will develop, modify, evaluate, and verify electronic components for medical devices. This is a unique opportunity to learn all areas of Stryker and to work with a variety of products. The project timeline is fast paced, and you will work to both solve problems and create efficiencies within the Stryker Instruments product lines. | 06/18/2025 |
| 1074 | Stryker Fort Lauderdale, FL Systems Engineer - DRE Bachelor of Science in Robotics, Electrical, Mechanical, Systems, or Biomedical Engineering Exp: 0+ years |
We’ve created new grad engineering roles within our DRE (Digital, Robotics and Enabling Technologies) organization in Weston, FL to invest in the next generation of innovators—accelerating their growth as engineers while building the future of Stryker. | 06/18/2025 |
| 1075 | Supernus Pharmaceuticals Rockville, MD Quality Control Chemist BS degree in Chemistry or other science-related discipline Exp: 1+ years |
Responsible for performing testing pharmaceutical solid dosage forms for release and stability, primarily by dissolution, and HPLC; maintaining proper GMP documentation for logbooks and report writing as necessary. | 06/18/2025 |
| 1076 | SystImmune Redmond, WA Research Associate/Senior Research Associate BS or MS in immunology, biochemistry, molecular biology, structural biology, or a related field Exp: 1+ years |
We are seeking a skilled Research Associate/Senior Research Associate with experience in utilizing display technologies (yeast/phage) in protein engineering, directed evolution, or binder discovery. This is a laboratory-based role that will be supporting protein engineering efforts in discovering novel binders and novel protein leads/scaffolds. The position will join a growing protein engineering team in an innovative organization and reports to the Director of Protein Engineering. The ideal candidate will be a quick learner with a broad experience set with direct expertise in a display technology and/or an adjacent field including but not limited to high throughput molecular biology, antibody/binder discovery, and protein engineering. Industry experience in biologics drug development is required. | 06/18/2025 |
| 1077 | SystImmune Redmond, WA Research Associate/Senior Research Associate - Cell Science Bachelor’s degree in biology or a related science major Exp: 1+ years |
Located in Redmond WA, Systimmune Inc.is a bio-pharmaceutical company focused on the treatment of cancer through developing novel therapeutic multi-specific antibodies, as well as antibody-drug conjugates (ADCs). Our objective is to create biologics that work through systematic intervention on the solid tumor micro-environment, to either directly attack the tumor and/or to activate the immune system to attack the tumor. We are seeking a Research Associate / Senior Research Associate with experience in cell culture and plasmid preparation to join our Cell Science Department. | 06/18/2025 |
| 1078 | TAE Life Sciences Santa Monica, CA Research Associate, Molecular Biology BS/MS in Molecular Biology, Cell Biology, Biochemistry or equivalent Exp: 1-3 years |
We are seeking a highly talented and motivated individual with a strong background in molecular/cell biology to join our Molecular Biology group in the pursuit of developing novel therapeutic agents. The successful candidate will be responsible for generating and evaluating product candidates, with focus on performing experiments using recombinant DNA technology and developing antibody library construction and screening platforms. This role works in a collaboration with Protein Science, Translational Research, and Chemistry/Bioconjugation groups, onsite in a lab environment. | 06/18/2025 |
| 1079 | Takeda Boston, MA Research Associate, Analytical Development Bachelor’s degree in biology, biomedical engineering, or related pharmaceutical science Exp: 1+ years |
The Research Associate will play an integral part in sample testing, data analysis, workflow streamlining, automation, and method technology transfers. The Research Associate will be highly motivated, a team player mindset, great attention to detail, a high emotional IQ, and a foundation in science. This role will contribute to developing and executing analytical methods crucial for ensuring the quality, safety, and efficacy of cell-based therapeutics. | 06/18/2025 |
| 1080 | Takeda Boston, MA Research Senior Associate, Cell Therapy Master’s degree in Biotechnology, Immunology, Molecular Biology, Biomedical Engineering or related scientific field or related field Exp: 1 year |
Takeda Development Center Americas, Inc. is seeking a Research Senior Associate, Cell Therapy with the following duties: Plan and independently execute in vitro experiments to deliver data for cell therapy discovery platforms; Scope of experiments include production of engineered human and mouse T cells, proof-of-concept studies, target identification and selection, lead optimization, and functional assessments; Adapt or develop, evaluate, and troubleshoot in vitro and ex vivo experimental techniques; Create, compile, analyze, and record experimental data; Review, interpret, and present results internally in research team and cross-departmental meetings; Serve as a technical resource in the laboratory for other employees by demonstrating techniques and preparing study protocols and internal technical transfer documentation; Utilize scientific literature to increase knowledge base and implement improvements; Assist with development of project strategy; up to 20% remote work allowed. | 06/18/2025 |
| 1081 | Takeda Boston, MA Research Senior Associate, Oncology Cell Therapy Master’s degree in Biotechnology or related field Exp: 1 year |
Takeda Development Center Americas, Inc. is seeking a Research Senior Associate, Oncology Cell Therapy with the following duties: maintain primary immune cell cultures and produce human and mouse CAR T cells. Plan, prioritize, and execute CAR gamma-delta T cell production, applying leadership qualities to facilitate a seamless workflow for experiments. Establish new experimental designs for CAR T cells co-cultured with differentially activated fibroblasts and other target cell types using a range of techniques and analytical method such as ELISA/MSD, flow cytometry, cytotoxicity readouts, and/or gene expression. Produce, titer, and bank viral vectors to express CAR and other constructs in T cells. Collaborate with project representatives to plan experiments, analyze and interpret data, and communicate findings internally. Prepare study protocols, reports, and documentation. Work with manager and teammates to troubleshoot complex problems in creative and effective ways. Actively participate in the innovation and optimization of cell therapy processes to ensure the delivery of project goals. Up to 20% remote work allowed. | 06/18/2025 |
| 1082 | Takeda Social Circle, GA Quality Validation Associate I Bachelor's degree in science, engineering or other related technical field Exp: 1+ years |
This position supports site projects, technical transfers, and ongoing validation maintenance. Primarily responsible for compliance during the review of the design, authorship, and execution of commissioning, qualification. This position is responsible to maintain validation documentation aligned with Good Documentation Practices (GDP) and ensure compliance with industry standards (e.g. FDA, EU GMP, ISO, etc). Provides technical subject matter expert (SME) support to change controls, investigations, deviations, and CAPAs. Individual must work on moderate to complex assignments, where analysis of situations or data requires an in-depth evaluation of various factors or intangible variables. | 06/18/2025 |
| 1083 | Tempus Chicago, IL Molecular Technologist I (Extractions) BS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 0-1+ years |
Work with a cutting-edge genomics workflow to provide high-quality data with rapid turnaround times in a clinical laboratory. Perform routine testing, quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform nucleic acid extraction and DNA/RNA quantification and qualification using robotics and automated liquid handlers. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Obtain 12 continuing education hours in the field of oncology or molecular biology. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 06/18/2025 |
| 1084 | Tempus Chicago, IL Quality Control Technologist I BS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work within a cutting-edge genomics workflow to provide quality control support in a high-volume clinical molecular laboratory. Help create and implement new equipment functionality for use by Tempus R&D and clinical lab staff while maintaining CLIA/CAP/NYS-DOH/ISO compliance. Complete Performance Qualifications (PQs), Preventive Maintenance (PM), relocation, and routine maintenance for all clinically approved molecular laboratory equipment. Collect and help analyze metrics. Investigate equipment related issues and help facilitate and implement corrective and preventative actions. Interact with lab management and personnel to provide training, troubleshoot issues, and prioritize QC tasks. Report significant findings/deviations and system deficiencies to lab management, as appropriate. Update SOPs and equipment records within the document control system, including creation/ revision/ review of internal SOPs and other quality documentation. Create and review protocols and qualification summaries. Support the Lab QC team with reagent and documentation tasks as needed. Monitor and respond to laboratory temperature excursions. | 06/18/2025 |
| 1085 | PTC Therapeutics Mountain View, CA Contract, Lab Technician, Biology B.S. in chemistry, biochemistry or biology Exp: 0-2 years |
The Contract, Lab Technician, Biology will aid in the management of the proprietary compound collection at the PTC Mountain View Research Site. This individual will be a key member of the research group, providing samples to internal and external collaborators. Additionally, the compound management technician will perform routine chemical and biological assays to support various programs. The successful candidate will be almost pathologically detail-oriented and thrive performing high precision work. The Contract, Lab Technician, Biology supports adherence to all regulatory requirements and company Standard Operating Procedures (SOPs) including as appropriate. | 06/10/2025 |
| 1086 | PTC Therapeutics Bridgewater, NJ Associate Scientist I, Biology (Biochemistry) Master’s degree in a scientific discipline Exp: 1-2 years |
The Associate Scientist I, Biology (Biochemistry) is responsible for performing scientific experiments that contribute to research and drug discovery activities at PTC. This position assists in the conduct of early-stage research, the goal of which is the identification of New Chemical Entities (NCEs), as well as the advancement of research programs from the identification of screening hits to advanced lead optimization. The incumbent is also responsible for communicating experimental results to his/her supervisor and the project team. The Associate Scientist I, Biology supports adherence to all regulatory requirements and company Standard Operating Procedures (SOPs) including as appropriate. | 06/10/2025 |
| 1087 | Purdue Pharma Wilson, NC Quality Specialist II, Chemist Raw Materials MS in Chemistry or closely related science Exp: 1 year |
Performs a variety of chemical analyses and GMP review of raw materials, packaging components, ancillary solutions, in-process samples, finished product and stability samples in accordance with cGMP, GLP, DEA and company policies and procedures. Assists in writing and performing method validations and method transfers. Assists in process validations. Conducts equipment validations IQs, OQs, PQs, and MQs, if necessary. Provides assistance and technical support to other groups with chemical testing needs and performs troubleshooting of analytical methods and instrumentation. | 06/10/2025 |
| 1088 | Purdue Pharma Wilson, NC Quality Specialist I, Chemist BA or BS degree in Chemistry or closely related science Exp: 6 months |
The Quality Specialist I, Chemist is responsible for supporting the operations and manufacturing process by performing routine and non-routine analytical testing and GMP review in support of the analysis of raw materials, packaging components, ancillary solutions, in-process samples, finished product method development and/or transfers, cleaning/process validations, and stability samples. Will follow standard procedures in accordance with cGMP, GLP, DEA and company policies and procedures. | 06/10/2025 |
| 1089 | QIAGEN Germantown, MD Metrology Technician BS/BA Exp: 1-3 years |
The Metrology Technician performs equipment calibration assignments using standard methods and processes. Required duties include: Set-up, calibration, testing, repair, inspection and maintenance of equipment and tools. Making adjustments, modifications or replacements as needed. Maintain and document calibration of all measurement equipment (in the Electronic Calibration Maintenance Management System). Creating, maintaining, and updating department SOPs and other documentation as required. Coordinate the execution of the calibration program to include event scheduling, performance, and oversight of service suppliers. Provide notification of calibration tasks with due dates. Coordinate calibration scheduling with equipment owners when needed. Oversee work by outside calibration contractors to ensure compliance with applicable procedures. Troubleshoots and solves calibration and maintenance problems of moderate scope and complexity requiring broad technical interpretation of defined procedures and practices. Responsible for ensuring on-going compliance to applicable quality and EHS regulations and standards (e.g., cGMP, FDA, ISO, IVDD, OSHA, etc.). | 06/10/2025 |
| 1090 | Quality Agents , MD Quality Assurance Specialist BS in a technical discipline (Engineering, chemistry, microbiology, biology) Exp: 0-2 years |
Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. Our Quality Assurance Specialists are leading service providers to our clients providing GMP support. The individual will coordinate validation activities with the client and meet timelines. | 06/10/2025 |
| 1091 | Quality Agents Rockville, MD Validation Engineer I BS in a technical discipline (Engineering, chemistry, microbiology, biology) Exp: 0-2 years |
Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. Our Validation specialists will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The validation specialist will evaluate the equipment/utility/system/procedures used in development, production, and holding of pharmaceutical products and determine a validation approach. The individual should have experience with current US and international regulations, guidance, industry best practice in one of the following areas of validation: facilities, utilities, and equipment qualifications, process validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the validation specialist must be approved by the client. | 06/10/2025 |
| 1092 | Quansys Biosciences West Logan, UT Formulation Specialist I Bachelor’s degree in Biology, Chemistry, Biotechnology, or related field Exp: 0-2 years |
A Production Associate I is responsible for meeting production schedules in a fast-paced, high throughput industrial setting. This may include the production immunoassay components, chemical buffers, biological diluents/reagents, coated plates, and/or assembled kits, for customer order fulfillment. They will be responsible, under supervision, to follow established SOPs in order to support the goals of the department. Some degree of professional latitude, creativity and self management is expected. This position may manage very specific aspects of the manufacturing process within the department. | 06/10/2025 |
| 1093 | Quansys Biosciences West Logan, UT Research Associate I Bachelor’s degree in life sciences, cellular and molecular biology, protein sciences or related field Exp: 1+ years |
A Research Associate I (RA I) is responsible for carrying out reagent and assay development activities in the laboratory, under supervision, working to achieve development project goals including data analysis and assay qualification. This is a laboratory position performing protein-based immunoassays on a routine basis with relatively high throughput (3-10 plates per day). Some degree of professional latitude, creativity and self management is expected. | 06/10/2025 |
| 1094 | QuidelOrtho Rochester, NY V&V Engineer I (R&D) B.S. Degree in Computer Science, Chemistry, Biochemistry, Biology, Engineering, or a related discipline Exp: 1-2 years |
As QuidelOrtho continues to grow, we are seeking a Verification and Validation Engineer I to help with formal verification and validation of complex medical devices under the regulations of the FDA. The individual will be part of an engineering team that is responsible for requirements based test design and execution of test procedures both in a virtual and lab environment. The team is highly collaborative and will require regular interactions in formal reviews, test planning activities, and working with software development to reproduce and verify system defects. | 06/10/2025 |
| 1095 | Quva Bloomsbury, NJ Microbiologist I - 1st Shift Bachelor’s Degree, Biology discipline Exp: 0-2 years |
Our Microbiologist I plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete training, you will be required to perform individual hands-on work in the sterility testing and/or endotoxin testing programs. This person provides scientific guidance and interpretation of microbiology results to QC and production management. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. | 06/10/2025 |
| 1096 | Reckitt St. Peters, MO Quality Compliance Associate B.S. degree in a science field preferably Chemistry Exp: 1-3 years |
Perform chemical and/or physical testing on all in-process, finished, validation, and R&D products according to applicable procedures while following all relevant laboratory Test Methods, SOPs, etc. Provide support for or perform calibration, laboratory investigations, and projects as required. Participate in advanced training on equipment and/or methods and assist as needed in validation and method development. | 06/10/2025 |
| 1097 | Regeneron Tarrytown, NY Sr Assoc Scientist - Immunology and Inflammation BS/MS Exp: 1-4 years |
Regeneron's Immunology and Inflammation group, located in Tarrytown, NY is looking for an energetic Sr Associate Scientist to join a highly collaborative team working in autoimmunity and/or allergy, B cell biology and disease models driven by pathogenic antibodies. | 06/10/2025 |
| 1098 | REGENXBIO Rockville, MD Clinical Research Associate Bachelors degree required; scientific discipline or related healthcare field Exp: 1 year |
As a Clinical Research Associate (CRA), you will be responsible for the support and coordination of the logistical aspects of clinical trial management, site management, data review & cleaning according to FDA regulations, Good Clinical Practice (GCP) and relevant SOPs. You’ll act as a pivotal point of contact for the clinical trial team and assist with the coordination of activities associated with the start-up, conduct, and close-out of clinical trials and other duties as assigned. | 06/10/2025 |
| 1099 | REGENXBIO Rockville, MD Sr. Clinical Trial Associate Bachelor's degree required preferably in a scientific discipline or related healthcare field Exp: 1-2 years |
As a Senior Clinical Trial Associate, you will be responsible for coordinating the logistical aspects of clinical trials and electronic Trial Master File (eTMF) support according to Good Clinical Practice (GCP) and relevant SOP’s. You’ll act as a pivotal point of contact for the clinical trial team and assist with the coordination of activities associated with the start-up, conduct, and close-out of clinical trials and other duties as assigned. | 06/10/2025 |
| 1100 | REGENXBIO Rockville, MD Associate Clinical Sample Manager Bachelor's degree required preferably in a scientific discipline or related healthcare field Exp: 1-2 years |
REGENXBIO is an exceptional place where some of the best of brightest people have the opportunity to collaborate, touch amazing science, and contribute toward extraordinary plans. As a Contract Associate Clinical Sample Manager, you will be provide support and coordination of the logistical aspects of clinical sample management which includes coordinating operational activities required to collect, track, and deliver clinical trial samples for all assigned clinical trials. You’ll also support the management of vendor contracts as applicable. This is a 6-month contract position with the potential to convert to permanent. | 06/10/2025 |
| 1101 | Repertoire Immune Medicines Cambridge, MA Research Associate I Bachelor’s or master’s degree (or equivalent) in scientific discipline or a health-related field Exp: 1+ years |
We are seeking a Research Associate to join our Platform Discovery Team. Some of the primary responsibilities of the RA will include preparation of in-house reagents required for our DECODE platform as well as the execution of next-generation sequencing experiments as well as downstream quality control. These activities will be performed both manually at the bench as well as with the help of liquid handling instrumentation. We are looking for an enthusiastic team player who will thrive in a fast-paced, dynamic, and highly collaborative environment. The RA will work as part of a cross-functional team of immunologists, molecular biologists, and protein scientists to successfully execute experiments and contribute to process optimization. This is a temporary, 6-month contract position. | 06/10/2025 |
| 1102 | Revolution Medicines Redwood City, CA Clinical Trial Assistant II Bachelor’s degree in biological sciences or related health related field Exp: 1-3 years |
As a Clinical Trial Assistant II in Clinical Operations, initially reporting to the Director Clinical Operations, you will be responsible for acting as a central contact for the clinical study teams and assist with the clinical execution and management to support RevMed clinical trials. | 06/10/2025 |
| 1103 | Revolution Medicines Redwood City, CA Clinical Trial Assistant II, Clinical Operations Process & Systems Bachelor’s degree in biological sciences or health-related field Exp: 1-3 years |
This is a unique opportunity for a Clinical Operations Professional. As the Clinical Trial Assistant II (CTA II), Clinical Operations Process and Systems, you will be responsible for acting as an integral member of the Clinical Operational Strategy & Process Optimization team and will be tasked to support the management of Clinical Operations processes and systems, in support of Clinical Operations and execution of RevMed’s clinical trials. | 06/10/2025 |
| 1104 | RION Rochester, MN Research Associate Bachelor’s or Master’s degree with focus in Biological Sciences Exp: 1+ years |
The Research Associate will contribute to ongoing scientific projects within the Research and Development laboratory focused on Rion’s exosome technology. As such, the candidate will possess the technical skills required to conduct experiments and assays in a wet lab environment involving techniques such as mammalian cell culture, flow cytometry, ELISA, RT-qPCR, and colorimetric/fluorometric-based assays. The Research Associate will be responsible for the execution of experiments, as well as data interpretation and final reporting. The position affords the opportunity to serve as a key member of Rion’s scientific team and contribute to the advancement of exosome therapeutics. The Research Associate will work closely with the Research and Development Scientists and support the efforts Process Development. As such, the successful candidate will work in an upbeat, highly collaborative and dynamic environment. Additional responsibilities associated with this position will involve assisting in day-to-day laboratory operations such as inventory management, procurement, and general laboratory and equipment maintenance. | 06/10/2025 |
| 1105 | Roche Nashville-Davidson, TN Field Engineering Specialist Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Chemistry or related field Exp: 1-2 years |
Roche Support Network offers an exciting opportunity for individuals who are passionate about problem-solving. As a research-focused healthcare company, Roche is dedicated to discovering, developing, and providing innovative diagnostics and therapeutic products. With a commitment to employee development and a work environment that values respect and empowerment, Roche offers exciting career prospects for those seeking to make a significant impact on patient care. | 06/10/2025 |
| 1106 | Roche Salt Lake City, UT Field Engineering Specialist Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Chemistry or related field Exp: 1-2 years |
Roche Support Network offers an exciting opportunity for individuals who are passionate about problem solving. As a research-focused healthcare company, Roche is dedicated to discovering, developing, and providing innovative diagnostics and therapeutic products. With a commitment to employee development and a work environment that values respect and empowerment, Roche offers exciting career prospects for those seeking to make a significant impact on patient care. | 06/10/2025 |
| 1107 | Roche Providence, RI Field Engineering Specialist- Molecular Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Chemistry or related field Exp: 1-2 years |
Roche Support Network offers an exciting opportunity for individuals who are passionate about problem solving. As a research-focused healthcare company, Roche is dedicated to discovering, developing, and providing innovative diagnostics and therapeutic products. With a commitment to employee development and a work environment that values respect and empowerment, Roche offers exciting career prospects for those seeking to make a significant impact on patient care. This role offers the opportunity to support our serology business, which plays a critical role in detecting antibodies and antigens to aid in diagnosing infections, ensuring blood safety, and monitoring immune responses | 06/10/2025 |
| 1108 | Roche Springfield, MA Field Engineering Specialist Bachelor's degree in a relevant field Exp: 1-2 years |
Roche Support Network offers an exciting opportunity for individuals who are passionate about problem-solving. As a research-focused healthcare company, Roche is dedicated to discovering, developing, and providing innovative diagnostics and therapeutic products. With a commitment to employee development and a work environment that values respect and empowerment, Roche offers exciting career prospects for those seeking to make a significant impact on patient care. | 06/10/2025 |
| 1109 | Roche Philadelphia, PA Lab Associate, Laboratory Operations BA/BS in biological sciences Exp: 0-3 years |
Support the day-to-day laboratory activities across Roche's Research and Technology facilities. Provide a safe and efficient workspace for scientific activities in close collaboration with the scientific laboratory staff, facilities, and inventory management personnel. | 06/10/2025 |
| 1110 | Roche Cincinnati, OH Field Engineering Specialist Bachelor's degree in a relevant field Exp: 1-2 years |
Roche Support Network offers an exciting opportunity for individuals who are passionate about problem-solving. As a research-focused healthcare company, Roche is dedicated to discovering, developing, and providing innovative diagnostics and therapeutic products. With a commitment to employee development and a work environment that values respect and empowerment, Roche offers exciting career prospects for those seeking to make a significant impact on patient care. | 06/10/2025 |
| 1111 | Roche Boston, MA Field Engineering Specialist Bachelor's degree in a relevant field Exp: 1-2 years |
Roche Support Network offers an exciting opportunity for individuals who are passionate about problem solving. As a research-focused healthcare company, Roche is dedicated to discovering, developing, and providing innovative diagnostics and therapeutic products. With a commitment to employee development and a work environment that values respect and empowerment, Roche offers exciting career prospects for those seeking to make a significant impact on patient care. | 06/10/2025 |
| 1112 | RoslinCT Hopkinton, MA Cell Processing Associate (3rd Shift) Bachelor's degree in biology or related scientific discipline Exp: 0-5 years |
This is a third shift role reporting to the Manufacturing Supervisor. The position's core responsibilities are focused on clinical and commercial manufacturing processes related to cell therapies. Activities include aseptic sampling of products in a Grade A environment, to operate automated, single-use systems for the targeting, expansion, and harvesting. Operate and maintain cell processing equipment. The Cell Processing Associate will support inventory management, suite cleaning, and setup activities per RoslinCT’s governing procedures. This position may require the individual to collaborate as needed with peers within Manufacturing Sciences and Technology (MS&T), Quality, and Facilities. | 06/10/2025 |
| 1113 | RoslinCT Hopkinton, MA QC Analyst II, Microbiology (3rd Shift) Bachelor's Degree in scientific discipline, Microbiology focus Exp: 0-7+ years |
The Quality Control Microbiology, QC Analyst will be responsible for collecting environmental samples in clean room areas to support manufacturing operations, sample management activities, and testing of cell therapy in-process and release product samples. The person will be responsible for reporting data and writing/revising standard operating procedures (SOPs) and test methods. This position will also provide support to assist the QC group and partner project teams during technology transfer, analytical method qualification, and routine GMP testing. The QC Analyst I/II, Microbiology will partner with the QC analytical team, interface with multiple groups including manufacturing, and must have the ability to assess method suitability, interpret results, perform tasks independently, and troubleshoot. Identifies and supports initiation and completion of deviations, corrective and preventative actions, and laboratory investigations in compliance with all applicable quality systems and current cGMPs. | 06/10/2025 |
| 1114 | RoslinCT Hopkinton, MA QC Analyst I/II, Analytical (3rd Shift) Bachelor's Degree in scientific discipline Exp: 0-5+ years |
The Quality Control Analytical, QC Analyst will be executing analytical methods such as appearance, pH, osmolality, cell counting, ELISAs, flow cytometry and related methods. This position will also provide support to assist the QC group and partner project teams during technology transfer, analytical method qualification, and routine GMP testing. The QC Analyst I/II, Analytical will partner with the analytical team, interface with multiple groups, and must have the ability to assess method suitability, interpret results, perform tasks independently, and troubleshoot. He/she will be responsible for authoring Standard Operating Procedures (SOPs), specifications and Test Methods. He/she will assist in the implementation of new assay methodologies and the associated instrumentation. Identifies and supports initiation and completion of deviations, corrective and preventative actions, and laboratory investigations in compliance with all applicable quality systems and current cGMPs. | 06/10/2025 |
| 1115 | RoslinCT Hopkinton, MA QC Analyst I/II, Analytical Bachelor's Degree in scientific discipline Exp: 0-5+ years |
The Quality Control Analytical, QC Analyst will be executing analytical methods such as appearance, pH, osmolality, cell counting, ELISAs, flow cytometry and related methods. This position will also provide support to assist the QC group and partner project teams during technology transfer, analytical method qualification, and routine GMP testing. The QC Analyst I/II, Analytical will partner with the analytical team, interface with multiple groups, and must have the ability to assess method suitability, interpret results, perform tasks independently, and troubleshoot. He/she will be responsible for authoring Standard Operating Procedures (SOPs), specifications and Test Methods. He/she will assist in the implementation of new assay methodologies and the associated instrumentation. Identifies and supports initiation and completion of deviations, corrective and preventative actions, and laboratory investigations in compliance with all applicable quality systems and current cGMPs. | 06/10/2025 |
| 1116 | RoslinCT Hopkinton, MA QC Analyst, Microbiology Bachelor's degree in scientific discipline Exp: 0-7+ years |
The Quality Control Analyst will be responsible for collection of environmental and raw material samples, sample management activities, and testing of cell therapy in-process, release and stability product samples. He/she will be responsible for reporting of data and writing/revising standard operating procedures (SOPs). He/she may support equipment onboarding and qualification as well as test method qualification in compliance with all applicable quality systems and current cGMPs. | 06/10/2025 |
| 1117 | Sai Life Sciences Watertown, MA Research Associate - Biology Bachelor's or Master's degree in Biology Exp: 1+ years |
As the Research Associate in Biology, you will play a crucial role in conducting groundbreaking research, contributing to our mission of advancing scientific knowledge and addressing pressing biological challenges. Working closely with our team of scientists, you will be involved in various aspects of experimental design, data collection, analysis, and interpretation. This position offers an exciting opportunity to be at the forefront of scientific discovery and make a meaningful impact in the field of biology. | 06/10/2025 |
| 1118 | Sai Life Sciences Watertown, MA Senior Research Associate - Biology Master's degree in Biology Exp: 1+ years |
As the Senior Research Associate in Biology, you will play a crucial role in conducting groundbreaking research, contributing to our mission of advancing scientific knowledge and addressing pressing biological challenges. Working closely with our team of scientists, you will be involved in various aspects of experimental design, data collection, analysis, and interpretation. This position offers an exciting opportunity to be at the forefront of scientific discovery and make a meaningful impact in the field of biology. You’ll have the opportunity to develop your skills to work independently and advance your knowledge-base on assay development and optimization. | 06/10/2025 |
| 1119 | Sanguine Biosciences Remote, Research Coordinator I, Translational Bachelor's Degree in a life science or other related field Exp: 1-2 years |
The role of the Research Coordinator I, Translational is to serve as a primary point of contact for potential donors in research studies and maintain all associated participant data. The Research Coordinator I is responsible for screening and qualifying donors who are part of an extensive Sanguine database, and those who are identified by the Patient Recruitment and Marketing Team. The Research Coordinator I will screen potential donors to obtain the necessary health information, and conduct medical record reviews to qualify donors for research studies. The Research Coordinator I may also have the opportunity to work on specific aspects of clinical trials and other research study types, as it relates to patient data, appointments and compliance. This role will work cross functionally with multiple departments including Project Management, Field Operations, and Apheresis Operations. This role will report to the Patient Operations Manager and will be a part of a service-centric and analytics-driven team that believes in empathy, compassion, and centering our focus on the needs of our donors. | 06/10/2025 |
| 1120 | Sanofi Waltham, MA Senior Research Associate, BioAnalytics (Biophysics) M.S. degree in Analytical Chemistry, Biochemistry, or related discipline Exp: 0-2 years |
We are seeking a motivated senior research associate to join our BioAnalytics Characterization group in the Genomic Medicine Unit within Sanofi. The Genomic Medicine Unit at Sanofi is dedicated to the establishment of best-in-class platforms to support development of life-changing advanced gene therapy products, including recombinant AAV vectors and lipid nanoparticles. The BioAnalytics Characterization group uses advanced analytical techniques for in-depth structural and functional characterization of gene therapy products in support of drug development, from pre-candidate selection through commercialization. | 06/10/2025 |
| 1121 | Sanofi Ridgefield, NJ Aseptic Technician II Bachelor's degree Exp: 1+ years |
Prefilled Syringe (PFS) Manufacturing is responsible for fill and finish of prefilled syringe products produced on the site. This includes hyaluronic acid (HA) based medical device products as well as pharmaceutical based products. In support of our main functions, additional responsibilities include cleaning and sanitization of process equipment. Based on production schedules, random and different start time scenarios may occur, so a very flexible work schedule is required for the candidate. Ability to accommodate production requirements that may require 50+ hour workweeks, including 2nd shift or split shift hours, extended day hours and weekends. This role requires frequent work on weekends depending on production demands. We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started? | 06/10/2025 |
| 1122 | Sanofi Pearl River, NY Quality Control Support Professional Bachelor's science degree ( Biochemistry, Chemistry, Biology, Molecular Biology, Immunology and or related disciplines) Exp: 1-2 years |
The role involves supporting quality control and project management at the Pearl River site, ensuring compliance with regulatory standards for environmental and microbiological contamination control. | 06/10/2025 |
| 1123 | Saptalis Hauppauge, NY Analytical Scientist B.S/M.S in Analytical Chemistry or related discipline Exp: 0-2 years |
Saptalis is looking to recruit Analytical Scientists to join the growing Analytical R&D group at our facility in Hauppauge, NY. Analytical Scientist is responsible for developing and validating analytical methods for analytes of interest in new drug products using UPLC, HPLC, GC and other analytical instruments. Execute all functions in accordance with current FDA regulations, ICH guide lines, USP methodologies, cGLPs and Saptalis SOPs. | 06/10/2025 |
| 1124 | Saptalis Hauppauge, NY Quality Control Scientist BS/MS Degree (chemistry or related field) Exp: 0-2 years |
Saptalis is looking to recruit QC Scientists to join the growing Quality group at our facility in Hauppauge, NY. QC Scientist is responsible for GMP testing of raw materials, in-process, finished product and stability samples for release. In addition, the responsibilities include maintaining laboratory equipment, assisting in investigations and coordinating external testing as needed. | 06/10/2025 |
| 1125 | Outpace Bio Seattle, WA Research Associate II/Senior Research Associate, Analytical Development M.S. in Biology, Biochemistry, Immunology, Molecular Biology, Analytical Chemistry, Biotechnology, or related disciplines Exp: 0-2+ years |
Outpace Bio is seeking an Research Associate II/Senior Research Associate to support development of analytical assays and technology transfer to CDMO partners for the GMP production of lentiviral vectors and CAR/TCR drug products. As a member of the Technical Operations team, the Research Associate II/Senior Research Associate will contribute to analytical development projects supporting CMC activities, authoring analytical development reports, advancing early phase analytical method transfer from the Outpace R&D team, and conducting hands-on, technical laboratory work. This position will report to the Senior Scientist, Analytical Development and will work closely with R&D functional groups (Platform, Immunology, CAR T development) as an integral part of project teams. Key contributions expected from this role include novel assay development, support for internal process and assay technology transfer to CDMOs and CROs, communications to internal and external stakeholders, and providing necessary technical support for regulatory submissions. | 06/03/2025 |
| 1126 | Padagis Minneapolis, MN Senior Quality Control Chemistry Testing Technician Bachelor's degree Exp: 1+ years |
We are hiring for multiple positions for QC Chemistry Technician II, 1st Shift, in New Hope, MN who performs inspection on a range of work to detect defects and maintain quality standards. who performs inspection on a range of work to detect defects and maintain quality standards. | 06/03/2025 |
| 1127 | Padagis Minneapolis, MN Senior Microbiology Testing Technician, Quality Control Bachelor of Science in Microbiology or related science Exp: 1+ years |
We are hiring for multiple Microbiologist II Technicians to support the Microbiological analysis of products, stability samples, validation samples, raw materials, and environmental samples through testing, data analysis/interpretation, method validation and continuous improvement projects. | 06/03/2025 |
| 1128 | Parexel West Point, PA Scientist III - Biophysical & Materials Analytical Characterization MS in chemistry, biology, or related field Exp: 1-2 years |
This is a laboratory-based scientific role in a fast-paced, multidisciplinary team environment, requiring the utilization of biophysical analytical characterization techniques to support development of vaccine drug substance and drug products in a GMP-like environment. The vaccine drug substance and product development support includes sample manipulation, equipment maintenance, routine analysis, and characterization of development vaccines to support process and formulation development. | 06/03/2025 |
| 1129 | Parexel West Point, PA Scientist II or III - Device Verification Scientist - FSP B.S. or M.S. Degree in Automated Sciences, Engineering, Chemistry, Biology or equivalent Exp: Scientist 2 - BS: 1-2 years or MS: 1+ years Scientist 3 - MS: 1-2 years |
We are looking to fill a Scientist 2 or 3- Device Verification Scientist position working as a full-time employee of Parexel on long-term assignment onsite at one of our clients located in West Point, PA. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer sponsorship. The Center for Packaging and Device Analytics (CPDA) provides physical analytical expertise in support of production and commercialization of packaging and combination device products. | 06/03/2025 |
| 1130 | Parexel Rahway, NJ Scientist II or III - Automation / Robotics Scientist MS or BS degree in chemical engineering, chemistry, biochemical engineering, or related applied science field Exp: Scientist 2 - BS: 1-2 years or MS: No Exp Scientist 3 - MS: 1-2 years |
We are looking to fill a position for a Scientist working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in Rahway, NJ. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer any sponsorship. | 06/03/2025 |
| 1131 | Parexel Rahway, NJ Scientist II or III - HPLC Separations Focus - FSP BS or MS Exp: Scientist 2 - BS: 1-2 years or MS: 0-1 years Scientist 3 - MS: 1-2 years |
We are looking to fill a position for a Scientist working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in Rahway, NJ. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer any sponsorship. | 06/03/2025 |
| 1132 | Parexel Rahway, NJ Engineer III - API Crystallization - FSP MS degree or equivalent in Engineering, Chemistry, Chemical Engineering, or a related field is required Exp: 1-2 years |
The Chemical Engineering Research and Development department of one of our clients in Rahway, NJ has a position available that will have primary accountability for lab process development specifically around API crystallization, isolation, drying, and particle physical attribute control. Activities will include working with gram quantities at the bench scale to a few kilograms at the Unit Operations and Preplab scales utilizing wet and dry processing equipment within these labs (e.g., crystallization vessels, filtration and drying equipment, and wet and dry milling tools, etc.). The department offers fast-paced, hands-on research that requires a high degree of technical skills and contributions. Secondary activities may include experiments and the use of instruments associated with process safety evaluation when needed, and the general support of Specialty Labs operations within the Chemical Engineering R&D Department. | 06/03/2025 |
| 1133 | Parexel West Point, PA Scientist III - Process Development & Characterization Support M.S. in Chemistry, Biology or similar life sciences Exp: 1-2 years |
We are looking to fill a Scientist III - Process Development and Characterization Support position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in West Point, PA. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer sponsorship. Support of standard analytical testing of samples from vaccines and large molecule process development/characterization. Other potential opportunities include method development/optimization. | 06/03/2025 |
| 1134 | Parexel Rahway, NJ Scientist III - Analytical Chemist - FSP M.S. in Chemistry, Chemical Engineering, Biochemistry, Biology or similar life sciences Exp: 1-2 years |
We are looking to fill a Scientist 3 –Analytical Chemist (Raw Materials) position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in Rahway, NJ. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. The position does not offer any sponsorship. Conduct raw materials release testing, and cleaning validation and cleaning verification testing, using a myriad of methodologies and techniques including separations sciences in a GMP laboratory. | 06/03/2025 |
| 1135 | PCI Rockford, IL Operations Process Engineer Bachelor's Degree in a related field Exp: 1-5 years |
This position will work to continuously improve processes and systems that ultimately lead to improved profitability to the company. Using all available Engineering, Lean, and Six Sigma tools, this position will work independently and cross-functionally to drive out waste and reduce process variability. | 06/03/2025 |
| 1136 | PCI San Diego, CA Quality Compliance Specialist Bachelor's Degree in a related field Exp: 1-5 years |
The Quality Compliance Specialist supports the site compliance and regulatory strategies necessary to support customer’s products as well as leading both regulatory inspections and customer audits. They are responsible for supporting the implementation of company policies and objectives involving matters of government and regulations, with respect to the FDA, DEA, and other ex-US regulatory agencies as applicable. The role will also provide support for client business reviews, investigations, complaints, CAPAs, inspections, quality metrics, and continuous improvement initiatives as required by the company supervisory responsibilities for the role. | 06/03/2025 |
| 1137 | Penumbra Alameda, CA Manufacturing Engineer I - Development Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering or related degree Exp: 1+ years |
The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and that support continuous improvement in production. Project opportunities are designed to develop professional work knowledge and abilities and to support the efforts and projects that have global importance to the success of the business. Area of work involves manufacturing processes with interaction between production and cross-departmental engineering groups in resolving problems encountered on the production floor and across the business. Evaluates, selects, and applies exciting engineering techniques, procedures, and criteria, using judgment in developing and implementing adaptations and modifications on the production line and to quality systems. | 06/03/2025 |
| 1138 | Penumbra Roseville, CA Manufacturing Engineer I - Metals Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering or related degree Exp: 1+ years |
The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and that support continuous improvement in production. Project opportunities are designed to develop professional work knowledge and abilities and to support the efforts and projects that have global importance to the success of the business. Area of work involves manufacturing processes with interaction between production and cross-departmental engineering groups in resolving problems encountered on the production floor and across the business. Evaluates, selects, and applies exciting engineering techniques, procedures, and criteria, using judgment in developing and implementing adaptations and modifications on the production line and to quality systems. | 06/03/2025 |
| 1139 | Penumbra Roseville, CA Manufacturing Engineer I -Catheters Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering or related degree Exp: 1+ years |
The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and that support continuous improvement in production. Project opportunities are designed to develop professional work knowledge and abilities and to support the efforts and projects that have global importance to the success of the business. Area of work involves manufacturing processes with interaction between production and cross-departmental engineering groups in resolving problems encountered on the production floor and across the business. Evaluates, selects, and applies exciting engineering techniques, procedures, and criteria, using judgment in developing and implementing adaptations and modifications on the production line and to quality systems. | 06/03/2025 |
| 1140 | Penumbra Roseville, CA Quality Engineer I Bachelor’s or Master's degree in an engineering or scientific discipline Exp: 1+ years |
As a Quality Engineer I, you will be charged with the quality behind Penumbra's game-changing medical devices used to address some of the world's toughest disease states! Unlike quality engineering roles in other companies, at Penumbra, we provide our quality engineers with highly technical problems to solve. Your efforts will directly impact the safety of patients around the world who use our products. You will apply your passion for creative problem solving throughout all stages of the process, from concept to commercialization and into continuous improvements. | 06/03/2025 |
| 1141 | Perrigo Holland, MI Validation Engineer I Bachelor's degree in Engineering, Chemistry, Pharmacy or a closely allied field Exp: 1 year |
Perrigo is now hiring for a Validation Engineer who will work out of our facilities in Holland, Michigan. The Validation Engineer will primarily be responsible for preparing and reviewing plans, protocols, reports, and studies associated with validation activities (Process, Packaging, Cleaning, and Equipment). | 06/03/2025 |
| 1142 | Personalis Fremont, CA Clinical Lab Associate 1, Sun-Th AM Shift BA/BS in a biological discipline Exp: 0-2 years |
At Personalis, we are transforming the active management of cancer through breakthrough personalized testing. We aim to drive a new paradigm for cancer management, guiding care from biopsy through the life of the patient. Our highly sensitive assays combine tumor-and-normal profiling with proprietary algorithms to deliver advanced insights even as cancer evolves over time. Our products are designed to detect minimal residual disease (MRD) and recurrence at the earliest timepoints, enable selection of targeted therapies based on ultra-comprehensive genomic profiling, and enhance biomarker strategy for drug development. Personalis is based in Fremont, California. | 06/03/2025 |
| 1143 | Personalis Fremont, CA Clinical Lab Associate 1, Th-M AM Shift BA/BS in a biological discipline Exp: 0-2 years |
At Personalis, we are transforming the active management of cancer through breakthrough personalized testing. We aim to drive a new paradigm for cancer management, guiding care from biopsy through the life of the patient. Our highly sensitive assays combine tumor-and-normal profiling with proprietary algorithms to deliver advanced insights even as cancer evolves over time. Our products are designed to detect minimal residual disease (MRD) and recurrence at the earliest timepoints, enable selection of targeted therapies based on ultra-comprehensive genomic profiling, and enhance biomarker strategy for drug development. Personalis is based in Fremont, California. | 06/03/2025 |
| 1144 | Personalis Fremont, CA Clinical Lab Associate 1, Tu-Sat AM Shift BA/BS in a biological discipline Exp: 0-2 years |
At Personalis, we are transforming the active management of cancer through breakthrough personalized testing. We aim to drive a new paradigm for cancer management, guiding care from biopsy through the life of the patient. Our highly sensitive assays combine tumor-and-normal profiling with proprietary algorithms to deliver advanced insights even as cancer evolves over time. Our products are designed to detect minimal residual disease (MRD) and recurrence at the earliest timepoints, enable selection of targeted therapies based on ultra-comprehensive genomic profiling, and enhance biomarker strategy for drug development. Personalis is based in Fremont, California. | 06/03/2025 |
| 1145 | Pfizer Sanford, NC Sr. Associate Scientist, QC Chemistry Bachelor's degree Exp: 0+ years |
The position will support the Pfizer Sanford, NC Quality Operations department by performing Quality Control activities associated with clinical and/or commercial product, raw materials, and validation. Key responsibilities are performing GMP tasks associated with maintaining compliant Quality Control and Stability laboratories; testing, analyzing, interpreting, and trending results; and creating, reviewing and approving documentation. Individual should have knowledge of current Good Manufacturing Practices (cGMP), Laboratory Information Management System (LIMS), Microsoft Office™ applications specifically Word and Excel, analytical techniques and instrumentation, Lean Six Sigma concepts, and Lean Labs. | 06/03/2025 |
| 1146 | Pii Hunt Valley, MD QMS Associate Bachelor's degree Exp: 1-2 years |
The QA Associate ensures compliance with CGMP and internal policies, procedures, and specifications. This position is responsible for performing a role in any one or more of the following functions: Quality Operations, Process Quality, Batch Release, Quality Management Systems, and Compliance in accordance with CGMP and related company SOPs, state, federal and local laws as applicable. | 06/03/2025 |
| 1147 | Pii Hunt Valley, MD Microbiologist (EM) B.S / M.S. in a life sciences discipline Exp: 0-2 years |
Executes the activities of QC Microbiology Laboratory by following approved microbiological and chemical test procedures and ensuring their delivery in an accurate and timely manner following proper safety precautions. | 06/03/2025 |
| 1148 | Quest Diagnostics Lenexa, KS Forensic Toxicology Laboratory Scientist I Bachelor’s Degree Exp: 1 year |
This position works within the Forensic Toxicology Laboratory and is responsible for all aspects of testing of donor specimens including specimen preparation and instrument operation. | 06/03/2025 |
| 1149 | Quest Diagnostics Chantilly, VA Sr. Associate Scientist (R&D Toxicology) MS degree in Engineering, Chemistry, Chemical Engineering, or a related field is required Exp: 1-3 years |
Participates on a team of scientists in the development and transfer of assays. Incumbent will work in the laboratory. | 06/03/2025 |
| 1150 | Quest Diagnostics Chantilly, VA Associate Scientist, Toxicology (LCMS) - Hybrid Master's degree Exp: 1 year |
Participates on a team of scientists in the development and transfer to manufacturing of processes to purify, characterize and modify enzymes, antibodies and other proteins. Candidate will be expected to work in the laboratory. | 06/03/2025 |
| 1151 | Pledge Therapeutics Canton, MA Research Associate, Immuno-Oncology MS Exp: 1-2 years |
We seek an enthusiastic and curious scientist interested in participating in all aspects of the hit-to-lead drug discovery process. The opening is at our new state-of-the-art facility in Canton, MA. The successful candidate will engage in the Immuno Oncology research areas of the company and will work with a successful team of international senior scientists located in the USA and EU. The ideal candidate will have great communication skills, excellent technical skills, exemplary attention to detail, and a passion for learning. This position will have the opportunity to make significant scientific contributions to numerous drug discovery projects. | 06/03/2025 |
| 1152 | Pledge Therapeutics Canton, MA Research Associate, Virology Bachelor’s or Master’s degree in biological sciences or a related field Exp: 0-2 years |
We seek an enthusiastic and curious scientist interested in participating in all aspects of the hit-to-lead drug discovery process. The opening is at our state-of-the-art facility in Canton, MA. The successful candidate will engage in the company’s virology research areas and work with a successful team of scientists in the USA and EU. The ideal candidate will have great communication skills, excellent technical skills, exemplary attention to detail, and a passion for learning. This position will have the opportunity to make significant scientific contributions to numerous drug discovery projects. | 06/03/2025 |
| 1153 | Thermo Fisher Chantilly, VA Field Service Engineer II (LCMS) Bachelor’s Degree in Sciences, Engineering, Electronics Exp: 1-3 years |
This role sits within our Unity Lab Service (ULS) organization, which provides a single source for integrated lab service, support, and supply management. Our customized service offerings and outstanding services have the flexibility and experience to uniquely address our customer’s business needs. Whether they are looking to arrange for service on a single instrument or are seeking resources to handle entire labs, there is a solution to meet their business requirements. | 06/03/2025 |
| 1154 | Thermo Fisher Chelmsford, MA Scientist II, Manufacturing Sciences M.Sc. in Chemistry or chemical engineering Exp: 1-3 years |
The Scientist II will make an impact by driving raw material second-sourcing projects, including conducting characterization studies and bench builds. Perform characterization studies and analyze organic or inorganic compounds, raw materials, and finished products. Execute bench experiments effectively and develop polymer products and related processes to meet performance specifications. | 06/03/2025 |
| 1155 | Thermo Fisher Chicago, IL Scientist - HPLC, GMP Masters degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology Exp: 0-2 years |
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. | 06/03/2025 |
| 1156 | Thermo Fisher Greenville, NC Sr Formulation Technician: Control Room & Lyophilizer Bachelor’s Exp: No exp |
The Sr. Formulation Technician will be able to perform tasks with little to no direction. They will provide guidance in the absence of the Lead Formulation Technician. They will be proficient in aseptic filling and manufacturing. This colleague follows written and verbal instructions using cGMP documents and operating equipment when performing the following duties. Shift hours are 6am-6pm on a 2-2-3 rotating schedule. | 06/03/2025 |
| 1157 | Thermo Fisher Richmond, VA Assistant Scientist Bachelor's degree (chemistry, biology, biochemistry, microbiology or similar life science degree) Exp: 0-1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 06/03/2025 |
| 1158 | Thermo Fisher Sunnyvale, CA Scientist I, Manufacturing Sciences Bachelor’s degree or higher in Chemistry Exp: 0-1 years |
The Scientist I, Manufacturing Sciences, will be responsible for the synthesis of functionalized resins used in columns. | 06/03/2025 |
| 1159 | Thermo Fisher Wilmington, DE Associate Scientist, Formulations Bachelor's degree in Biological Sciences, or other related degree concentration Exp: 1-2 years |
The associate scientist will perform a variety of routine to complex lab activities related to formulation and overall drug product development of large molecule drug products. The role involves designing and executing the experiments, document experimental details, organize the data, and summarize the findings in a technical summary report. The position emphasizes scientific rigor, collaboration with different functions, and effective communication of findings within the organization. | 06/03/2025 |
| 1160 | PROCEPT BioRobotics San Jose, CA Associate Equipment Engineer BS in an Engineering discipline such as mechanical, Biomedical, or electrical engineering Exp: 6 months |
Are you ready to embark on an exciting journey that will revolutionize the way men suffering from BPH are treated? Join us as Director of Manufacturing Engineering and be at the forefront of producing a best-in-class therapy and technology that promises to become the standard of care for BPH. Your mission? Lead the Manufacturing Engineering team for Capital Equipment in both sustaining and improving the production operation for the Hydros and Aquabeam robotic systems but also supporting new product introduction for the next generation systems and all future Capital Equipment. This isn't just any job - it's a chance to make a real difference. We need a technical leader with the vision to guide production operations larger scale and capacity while maximizing the quality and performance of every system produced. We are looking for someone with the leadership skills to create a premier engineering team and build a cross-functional team dynamic that optimizes development and operational speed with a product quality unmatched in the space. Vision, technical acumen, high energy, communication, integrity and honesty will all be needed to succeed in this role and what we value at Procept. Get ready to transform lives and shape the future of healthcare! | 06/03/2025 |
| 1161 | Proclinical Cambridge, MA Quality Assurance Specialist Bachelor's degree in a scientific discipline (e.g., Biology, Chemistry, Engineering) Exp: 1-3 years |
We are on the hunt for bold, innovative thinkers who are ready to help push the boundaries of science and make a tangible difference in the world. The successful candidate will focus on document management and quality operations within the cardiovascular pharmaceuticals sector. Your expertise will support continuous improvement initiatives and ensure compliance with industry standards. | 06/03/2025 |
| 1162 | PSC Biotech York, PA QC Analyst I Bachelor’s degree in related science discipline, i.e. Chemistry, Microbiology. Exp: 1-3 years |
We are hiring an entry-junior level QC Analyst I. The QC Analyst I will be responsible for conducting quality control testing in the and ensuring the safety, efficacy, and consistency of products. This role involves rigorous analysis at every stage to ensure compliance with regulatory standards and internal quality guidelines. | 06/03/2025 |
| 1163 | PSC Biotech Remote, Validation Engineer I Bachelor's degree in related engineering discipline Exp: Entry Level |
This position will support system validation and product release processes, ensuring compliance with industry standards and regulatory requirements. You will play a key role in contributing to the development and improvement of validation procedures and driving overall product excellence. This is an entry-level, remote position. Successful candidates have a bachelor’s degree within an engineering discipline, a passion for technology, and exposure to system/software testing in the life science industry. | 06/03/2025 |
| 1164 | PSC Biotech York, PA Metrology Technician I Bachelor's degree in engineering or related technical field Exp: 0-1 years |
We are hiring an entry to junior level Metrology Technician responsible for conducting routine calibration tasks in alignment with established protocols and regulatory mandates. The position adeptly handles troubleshooting and equipment repair as needed, while ensuring the steadfast adherence to quality system compliance standards. | 06/03/2025 |
| 1165 | Natera Austin, TX QC Reagent Assoc 1 BS/BA degree (or equivalent) in Biological Sciences, Biology, Chemistry or a related field Exp: 1+ years |
Support the activities for reagents used in the Operations Department’s Clinical Laboratories. Executes the preparation and qualification of molecular diagnostic reagents. Performs Quality Control tests on new incoming shipments of raw materials and small-scale manufacturing procedures (formulations and dispensing) reagent. Reviews data obtained for compliance to specifications and reports abnormalities. Maintains and improves QC documentation pertaining to raw material specification, reagent qualification, and QC testing. Support Incoming Quality Control activities as needed. | 05/28/2025 |
| 1166 | Natera San Carlos, CA Senior Service Engineer BS/BA in a biological science/biomedical engineering, similar field of study Exp: 1-3 years |
The Instrument Support Engineer is responsible for the service and support of laboratory equipment and instrumentation utilized in the Operations laboratory. The scope of support includes installation, calibration, maintenance, and repair of both simple (e.g., plate sealers) and complex (e.g., liquid handling robotics) instrumentation in the laboratory. The Instrument Service Engineer will be the primary point of contact for production lab personnel when equipment and instruments are not operating or not meeting operational specifications. | 05/28/2025 |
| 1167 | Natera San Carlos, CA Research Associate BS/BA in a biological science or equivalent Exp: 1-2 years |
The Research Associate 1, performs laboratory procedures of varying complexity contributing to cross functional activities as part of the Sample Processing team. Works primarily with R&D Scientific Operations, a multidisciplinary team within the research and development department. | 05/28/2025 |
| 1168 | Natera Austin, TX Research Associate 1 Bachelor’s degree in Biological Sciences, Biotechnology, Molecular Biology, or a related field Exp: 0-2 years |
We are seeking a highly motivated and skilled Research Associate 1 to join our dynamic team in sample management. In this role, you will be responsible for the management of biological samples, ensuring their integrity, overseeing quality control, and supporting research projects that rely on biological specimens. The ideal candidate should have a strong background in bio-sample management, research methodologies, and data analysis, with an interest in contributing to cutting-edge scientific research. | 05/28/2025 |
| 1169 | Neuralink Austin, TX Mechanical Engineer, Surgery Engineering Bachelors Degree in Mechanical Engineering or Industrial Engineering Exp: 1-3 years |
The Surgery Engineering team is responsible for developing and managing custom hardware and processes for neurosurgical procedures, excluding the R1 Robot and Operator Station. Their responsibilities encompass the entire surgical process, including patient positioning, incision management, craniectomy, precise implant placement, thread management during robot-assisted insertion, surgical site irrigation, implant installation, and closure. Additionally, the team ensures safe explantation and upgrade procedures for implants. They also provide mechanical engineering support to the animal care, histology, and BCI teams, contributing to the success of complex neurosurgical procedures and related research activities. | 05/28/2025 |
| 1170 | Neurocrine Biosciences San Diego, CA TEMP - Associate Scientist / Scientist, Biologics Characterization, Biologics Lead Optimization Bachelor's degree in relevant scientific discipline Exp: 1-5+ years |
We are in search of a collaborative, passionate scientist with sound scientific knowledge and excellent technical skills in cell-based in-vitro assays, molecular biology and analytical sciences for AAV gene therapy and biologics. In the biologics lead optimization team, you will be responsible for performing routine analytical tests and developing/optimizing analytical methods to support the development and manufacturing of AAV based gene therapy products and biologic therapeutics. In this role, you will collaborate across multiple groups including process development, CMC, research, as well as CROs to ensure all applicable analytical test methods are appropriate for the stages of preclinical & clinical development. This is an excellent opportunity to utilize, contribute and advance the ideal candidate’s laboratory skills in a progressive, state-of-the-art and diverse facility. | 05/28/2025 |
| 1171 | NextPhase Mansfield, MA Mechanical Engineer Bachelor's Degree in Mechanical Engineering (B.S., M.E.) Exp: 1-4 years |
The Mechanical Engineer I will collaborate with team members to design and refine cutting-edge medical devices, contributing to product testing, validation, and optimization. Working closely with management, quality assurance, supply chain, and engineering teams, the Mechanical Engineer will oversee all stages of product development, encompassing mechanical design, materials sourcing, prototype fabrication, and the planning and implementation of characterization tests. Responsibilities will also include the development of test protocols, active participation in product testing, and the preparation of comprehensive test reports | 05/28/2025 |
| 1172 | Avecia Milford, MA Research Scientist I, Analytical Development MS Exp: 1+ years |
The Research Scientist I is responsible for meeting the analytical testing requirements to support research and development projects primarily focused on oligonucleotides. | 05/28/2025 |
| 1173 | Avecia Milford, MA Quality Control Analyst I BS in chemistry, biology or related discipline Exp: 0-2 years |
The QC Analyst I is responsible for conducting routing analysis of raw materials, in-process samples, and finished products in a strict GMP setting. The position involves working in the QC laboratory and in the manufacturing space on assigned tasks following written procedures and verbal instructions. | 05/28/2025 |
| 1174 | NJ Bio Princeton, NJ Scientist, Process Development MS level in Organic Chemistry Exp: 0-2 years |
Under minimal supervision works on multiple steps/multiple projects to execute chemical syntheses from mgs to grams to kilo scales and conduct pilot scale synthesis (kilo scale), purification and characterization of compounds and present results and progress updates to internal and external stakeholders, stay abreast of current literature in scientific areas, maintain equipment, chemical inventory and lab support and Perform duties as required. The incumbent works cross-functionally with internal departments and external resources on process development related issues. The Scientist, Process Development supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate. | 05/28/2025 |
| 1175 | NJ Bio Princeton, NJ Manufacturing Associate I BA/BS degree in a scientific discipline (synthetic /organic chemistry) Exp: 0-2 years |
The Manufacturing Associate I is responsible for the execution of production activities for early phase small molecule and/or biological programs within a GMP environment. The incumbent works cross-functionally with internal departments and external resources on manufacturing related issues. The Manufacturing Associate I supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate. | 05/28/2025 |
| 1176 | NJ Bio Princeton, NJ Assistant Project Manager BS, MS in Chemistry, Biochemistry, Biology, Health Sciences, or other related disciplines Exp: 0-2 years |
We are looking for a dedicated and detail-oriented Assistant Project Manager to join our team. The successful candidate will be responsible for supporting project management activities, ensuring projects are completed on time, within scope, and on budget, while maintaining high levels of customer satisfaction and collaboration. This position requires it to be onsite the vast majority of the time. The incumbent works cross-functionally with internal departments and external resources on project management related issues. The Assistant Project Manager supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate. | 05/28/2025 |
| 1177 | NorthStar Medical Radioisotopes Beloit, WI Radiopharmaceutical Manufacturing Associate (3rd Shift) Bachelor's Degree in a STEM discipline Exp: 1 year |
The Radiopharmaceutical Manufacturing Associate performs duties to support the development and manufacturing of radiopharmaceuticals for NorthStar operations. This includes equipment preparation, product dissolution, and dispensing of medical radioisotopes while complying with procedures, instructions, and prescribed routines. All duties and responsibilities will be completed in compliance with applicable regulatory agency standards. This position supports production in a 24-hour manufacturing facility which means your schedule provides days off during the week when weekend work is required. Early morning, late evening, weekend, and some holiday work will be required with occasional overtime. Requirements for this position include the ability to work 1st, 2nd, and 3rd shifts during the training period (several months). | 05/28/2025 |
| 1178 | Nova Biomedical Waltham, MA Quality Engineer I BS degree in engineering, the sciences, or another technical discipline. Exp: 1-2 years |
Nova Biomedical is hiring a Quality Engineer I on-site (hybrid) in our Waltham, MA facility. This role will support Quality Assurance activities within the corporate Quality Management System (QMS). Responsibilities include providing expertise and general oversight for the management and improvement of design and development, validations, quality planning, internal auditing, investigations, process controls, change management, quality records, corrective and preventive activities, data management, employee training, and other duties as assigned. | 05/28/2025 |
| 1179 | Nova Biomedical Billerica, MA Quality Engineer I BS degree in engineering, the sciences, or another technical discipline. Exp: 1-2 years |
Nova Biomedical is hiring a Quality Engineer I in our Manning Road, Billerica, MA facility. This role will support Quality Assurance activities within the corporate Quality Management System (QMS). Responsibilities include providing expertise and general oversight for the management and improvement of design and development, validations, quality planning, internal auditing, investigations, process controls, change management, quality records, corrective and preventive activities, data management, employee training, and other duties as assigned. | 05/28/2025 |
| 1180 | Novo Nordisk West Lebanon, NH Quality Control Analyst I - III Raw Materials - Methods Validation Bachelor’s degree in scientific discipline Exp: 1 year |
This position has primary responsibility to support Quality Control operations in the microbiology, analytical or inspection area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. This position carries out routine QC testing and may support sampling, investigations, validations, projects and other related support activities for the manufacturing facility and process. This individual works with supervision on routine tasks and detailed instruction on new tasks. | 05/28/2025 |
| 1181 | Novo Nordisk West Lebanon, NH Manufacturing Technician I - IV - BEN Bachelors’ Degree in a science discipline Exp: 0 years |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. | 05/28/2025 |
| 1182 | Novo Nordisk West Lebanon, NH Quality Control Analyst I - IV Micro Bachelor’s degree in scientific discipline Exp: 1 year |
This position has primary responsibility to support Quality Control operations in the microbiology, analytical or inspection area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. This position carries out routine QC testing and may support sampling, investigations, validations, projects and other related support activities for the manufacturing facility and process. This individual works with supervision on routine tasks and detailed instruction on new tasks. | 05/28/2025 |
| 1183 | Novo Nordisk Bloomington, IN Engineer, PM & Tech Transfer Bachelor’s degree in Engineering Exp: 1+ years |
This role will be responsible for the technical transfer of processes from Process Development or our clients. It will also involve drafting and review of documentation, compilation, and assessment of process data, and providing technical input for deviation investigations, change controls, and CAPAs. This role will provide on-call and on-the-floor technical support to manufacturing. This position will be client-facing and should possess the ability to work collaboratively with clients and internal cross-functional stakeholders to move projects forward. | 05/28/2025 |
| 1184 | Novonesis Milwaukee, WI Phage Lab Technician I Bachelor’s degree in microbiology, biology, biotechnology, or a related field Exp: No exp |
As a Phage Lab Technician, you'll gain hands-on experience in a dynamic environment focused on customer support through our phage testing service. | 05/28/2025 |
| 1185 | Novonesis Wausau, WI Quality Control Associate Bachelor’s Degree in Microbiology, Biology, Molecular Biology, Chemistry or related field Exp: 1-3 years |
The Quality Control Team ensures Novonesis delivers high-quality products by maintaining strict adherence to quality, safety, and compliance standards. Their work directly supports the company’s mission of innovation and customer satisfaction. The team fosters a collaborative environment, sharing knowledge and supporting one another in tackling challenges. Together, they conduct inspections, analyze manufacturing data, perform routine testing, and maintain compliance documentation, while also contributing to cross-functional projects aimed at process and product improvement. Looking forward, the team will focus on adopting advanced technologies like automation, predictive analytics, and digital tools to enhance efficiency. They will also play a key role in sustainability initiatives, ensuring compliance with green standards and reducing waste. By combining teamwork, technical expertise, and innovation, the Quality Control Team drives Novonesis’s commitment to excellence and continuous improvement. | 05/28/2025 |
| 1186 | Novonesis Franklinton, NC Recovery Engineer II BS in Chemical Engineering or related field Exp: 1+ year |
Lead recovery optimization in lab and production scale. Provide technical support for troubleshooting efforts and process improvement initiatives. Identify and capture new opportunities for production process improvements. Contribute to closing global gaps on focus products. Ensure projects are aligned with Global Optimization Network guidelines. Lead and motivate project teams towards achieving ambitious yet achievable goals. Support the professional development of peers through scientific guidance. Plan and coordinate experimental work for small and large-scale trials. Conduct experiments and evaluate data to ensure project expectations and deadlines are met. Effectively communicate technical insights and project progress. Recommend improvements in recovery pilot scale equipment and processes | 05/28/2025 |
| 1187 | Novonesis Salem, VA Process Engineer Bachelors degree in an engineering discipline Exp: 1+ years |
In this role you will be responsible for supporting production processes of microbial intermediates and finished goods, as well as supporting capital investment projects. The main aspects of this role include optimization of existing processes and parameters, support and qualification of new product launches at production scale, troubleshooting and structured problem solving for daily process/product support, adhering to and enforcing site safety, environmental, and quality policies, and serving as a technical resource (user manager) for small and mid-sized capital investment projects. | 05/28/2025 |
| 1188 | Nucleus Biologics San Diego, CA Manufacturing Technician I BS/BA in Biology/Immunology Exp: 1+ years |
The Manufacturing Technician I will assist the Manufacturing team and report into the Associate Manufacturing Manager. This individual will sit out of our San Diego, California. | 05/28/2025 |
| 1189 | Nucleus Radiopharma Rochester, MN Quality Assurance Associate Bachelor’s degree in Life Sciences, Quality, or a related field Exp: 0-2 years |
The Quality Assurance (QA) Associate will support the execution and maintenance of our Quality Management System (QMS). This role focuses on quality systems activities including deviation and CAPA coordination, change control tracking, and document control support. They will also assist in the creation of training materials to support GMP and quality compliance initiatives. | 05/28/2025 |
| 1190 | Nurix Therapeutics Woodlands, TX Research Associate I/II, Analytical Development & Quality Control MS Exp: 1+ year |
Nurix Therapeutics seeks a motivated Research Associate to join the Analytical Development and Quality Control group. The Research Associate will operate and maintain lab equipment and instrumentation, conduct sample receipt/analysis/data reporting, and communicate analytical results internally. | 05/28/2025 |
| 1191 | Nurix Therapeutics San Francisco, CA Research Associate I, Pharmaceutical Development (Contactor) BS/BA or higher in chemistry, pharmaceutics, or related field Exp: 1-2 years |
Nurix is looking for a Research Associate, Pharmaceutical Development to provide scientific, technical, and hands-on support of drug discovery and product development related to small molecules from early discovery to clinical trial enabling studies. | 05/28/2025 |
| 1192 | Globus Medical Limerick, PA Associate Quality Engineer Bachelor’s Degree required (science or engineering preferred) Exp: 0-2 years |
The Associate Quality Engineer will be responsible for achieving the highest quality level of manufacturing quality and quality system performance while ensuring compliance with all company policies and procedures and maintaining compliance with US FDA and international medical device regulations and ISO 13485 quality system requirements. As a contributor to the quality engineering organization, this professional will be a self-motivated and characterized as an excellent problem solver. This person will play an integral role in maintaining and improving the quality management system, product quality, and manufacturing process quality. | 05/28/2025 |
| 1193 | Globus Medical West Carrollton, OH Industrial Engineer Master's Degree Exp: No exp |
As an Industrial Engineer you will be responsible for driving operational excellence by analyzing workflows, optimizing production processes, and implementing Lean manufacturing principles to enhance safety, efficiency, and productivity. The successful candidate will lead initiatives to develop efficient plant layouts, establish and maintain labor standards, and drive continuous improvement across production operations. In addition to technical expertise, this role requires exceptional problem-solving skills, a proactive mindset, and the ability to influence and collaborate with cross-functional teams. The ideal candidate is a champion of Lean principles, committed to fostering a culture of continuous improvement while delivering measurable results in safety, quality, delivery, and cost. | 05/28/2025 |
| 1194 | Globus Medical Audubon, PA Electrical Engineer MS EE Exp: 1+ years |
We are seeking a highly skilled and motivated Electrical Engineer to join our rapidly growing Digital Health team. You will work closely with a dynamic team of electrical, software, and mechanical engineers to conceptualize and commercialize innovative medical devices to meaningfully impact the lives of patients with musculoskeletal disorders. The ideal candidate will have a strong background designing, building, and testing embedded electrical systems, including firmware design and development. This role requires a balance of creative thinking, analytical design, hands-on prototyping and testing, and systematic product development. | 05/28/2025 |
| 1195 | Ofni Systems Raleigh, NC Computer Systems Validation Engineer BS in math, science or engineering Exp: 1 year |
We are hiring a Validation Engineer to be on the cutting edge of automated validation techniques. You will be responsible for implementing our validation solutions while working with industry-leading companies. Ideal candidates are experts on the requirements of 21 CFR 11, have excellent critical thinking and interpersonal skills, and are motivated to meet client needs for compliance. If you are an A-level engineer who enjoys the challenge of solving real-world compliance problems then we would like to talk with you. | 05/28/2025 |
| 1196 | Olympus Charleston, SC Field Service Engineer I Bachelor’s degree Exp: 1-3 years |
The Field Service Engineer (FSE) services and maintains all product lines for Olympus America medical products. Under supervision of Manager and Senior FSE Trainer, the FSE will service and provide expert level technical support to assigned equipment. | 05/28/2025 |
| 1197 | Olympus Charlotte/Asheville/Greensboro, NC Field Service Engineer I Bachelor’s degree Exp: 1-3 years |
The Field Service Engineer (FSE) services and maintains all product lines for Olympus America medical products. Under supervision of Manager and Senior FSE Trainer, the FSE will service and provide expert level technical support to assigned equipment. | 05/28/2025 |
| 1198 | Olympus san Jose, CA Repair Engineer I Bachelor's degree in engineering Exp: 1 year |
Provide engineering support for introduction of new products and alternate repair activities. Function as Project Coordinator on more complicated projects as defined by the Manager by providing technical information to other project participants recommending cost effective procedures tracking and maintaining implementation dates and documenting completed projects. Provide support to Associate Engineer on his/her assigned projects. | 05/28/2025 |
| 1199 | Orca Bio Sacramento, CA Cell Therapy Production Associate, Oncology, 1st Shift B.S. degree in Biological or related sciences Exp: 1 year |
This is a 1st shift-based position, working on-site Monday through Friday, from 7am-3:30pm. The Cell Therapy Production Associate, Oncology plays a critical role in the production of Orca Bio’s life-saving cell therapy products, ensuring adherence to strict quality standards, regulatory requirements and aseptic production techniques. Reporting into the assigned manufacturing shift supervisor, the job involves repeatedly executing manufacturing processes, cleaning and maintaining production equipment and workstations and documenting production activities in a highly regulated environment. The role collaborates closely with Materials Management, Quality Control (QC), and Quality Assurance (QA) to carry out GMP manufacturing runs as part of a cross-functional team. | 05/28/2025 |
| 1200 | Orca Bio Sacramento, CA Cell Therapy Production Associate, Oncology, 2nd Shift B.S. degree in Biological or related sciences Exp: 1 year |
This is a 2nd shift-based position, working on-site Monday through Friday, from 3pm to 11:30pm. The Cell Therapy Production Associate, Oncology plays a critical role in the production of Orca Bio’s life-saving cell therapy products, ensuring adherence to strict quality standards, regulatory requirements and aseptic production techniques. Reporting into the assigned manufacturing shift supervisor, the job involves repeatedly executing manufacturing processes, cleaning and maintaining production equipment and workstations and documenting production activities in a highly regulated environment. The role collaborates closely with Materials Management, Quality Control (QC), and Quality Assurance (QA) to carry out GMP manufacturing runs as part of a cross-functional team. | 05/28/2025 |
| 1201 | Orca Bio Sacramento, CA Cell Therapy Production Associate, Oncology, 3rd Shift B.S. degree in Biological or related sciences Exp: 1 year |
This is a 3rd shift-based position, working on-site Monday through Thursday, from 9pm to 7:30am. The Cell Therapy Production Associate, Oncology plays a critical role in the production of Orca Bio’s life-saving cell therapy products, ensuring adherence to strict quality standards, regulatory requirements and aseptic production techniques. Reporting into the assigned manufacturing shift supervisor, the job involves repeatedly executing manufacturing processes, cleaning and maintaining production equipment and workstations and documenting production activities in a highly regulated environment. The role collaborates closely with Materials Management, Quality Control (QC), and Quality Assurance (QA) to carry out GMP manufacturing runs as part of a cross-functional team. | 05/28/2025 |
| 1202 | Orca Bio Sacramento, CA Specialist, Quality Assurance Master’s degree in a relevant scientific discipline (biology, biochemistry, immunology, etc.) Exp: 1+ years |
The Specialist, Quality Assurance position is a key role in meeting the quality policy through their management of the different quality systems, including production records and deviation system management. The ideal candidate will be responsible for managing the quality systems, including deviations, change control, corrective and preventive actions (CAPA), and document management. Additionally, this role involves making timely batch disposition decisions to ensure quality standards are met before product release, supporting the rapid processing times required by our product. You will have the unique opportunity to make a difference in the lives of many patients as Orca Bio develops next-generation cell therapies. | 05/28/2025 |
| 1203 | Organogenesis Canton, MA Production Associate I - Apligraf Bachelor’s degree in biology or related science Exp: 0-2 years |
This is an entry level position. The Associate will perform all activities involved in the aseptic processing of a living product (Apligraf), under the direct supervision of the Apligraf Team Leader/Apligraf Supervisor/Manager. The Apligraf Associate I will support the Apligraf Manufacturing department by performing the tasks that will assure the safe and timely processing of Apligraf, working in both a Class 100 and Class 10K cleanroom. | 05/28/2025 |
| 1204 | Organogenesis Smithfield, RI Production Associate Dermagraft Bachelor’s degree in biology or related science Exp: 0-2 years |
This is an entry level position. The Associate will perform all activities involved in the aseptic processing of a living product (Dermagraft), under the direct supervision of the Dermagraft Team Leader/Dermagraft Supervisor/Manager. The Dermagraft Associate will support the Dermagraft Manufacturing department by performing the tasks that will assure the safe and timely processing of Dermagraft, working in both a ISO 7 and ISO 8 cleanrooms. | 05/28/2025 |
| 1205 | RoslinCT Hopkinton, MA QC Analyst, Microbiology Bachelor's degree in scientific discipline Exp: 0-7+ years |
The Quality Control Analyst will be responsible for collection of environmental and raw material samples, sample management activities, and testing of cell therapy in-process, release and stability product samples. He/she will be responsible for reporting of data and writing/revising standard operating procedures (SOPs). He/she may support equipment onboarding and qualification as well as test method qualification in compliance with all applicable quality systems and current cGMPs. | 05/19/2025 |
| 1206 | RoslinCT Hopkinton, MA Project Engineer Associate Master's degree in engineering/science Exp: 1+ years |
The Project Engineer will execute and provide engineering support for the procurement, enrollment, and installation of equipment and systems. They will also support validation and commissioning activities. This critical role will develop and review related documentation and collaborate with Quality Assurance to ensure adherence to world-wide regulatory requirements and corporate standards. | 05/19/2025 |
| 1207 | RoslinCT Hopkinton, MA Cell Processing Associate Bachelor's degree in biology or related scientific discipline Exp: 0-5 years |
This is a third shift role reporting to the Manufacturing Supervisor. The position's core responsibilities are focused on clinical and commercial manufacturing processes related to cell therapies. Activities include aseptic sampling of products in a Grade A environment, to operate automated, single-use systems for the targeting, expansion, and harvesting. Operate and maintain cell processing equipment. The Cell Processing Associate will support inventory management, suite cleaning, and setup activities per RoslinCT’s governing procedures. This position may require the individual to collaborate as needed with peers within Manufacturing Sciences and Technology (MS&T), Quality, and Facilities. | 05/19/2025 |
| 1208 | Mallinckrodt Greenville, IL Process Engineer B.S in Engineering, Chemical Engineering or related field. Exp: 1-3 years |
The Process Engineer is the recognized technical leader for manufacturing processes and for the improvement of existing processes. Consistently seeks for and evaluates methods to improve overall customer satisfaction through improved manufacturing efficiencies. Serve as main point of contact for manufacturing processes in their area in regard to safety, quality, and continuous improvement activities. Ensure that the goals and objectives are achieved as they pertain to Safety, Quality, Production, Cost Standards, and Operational Excellence. | 05/19/2025 |
| 1209 | Mallinckrodt Raleigh, NC Quality Analyst II Bachelors or Sciences (BS) or equivalent life science degree Exp: 1-3 years |
The Quality Analyst II has responsibility for Product Release and Maintenance of Monthly Quality Metrics and Daily Notification to Management. They provide support for customer inquiries, gap assessments, batch record review, and label preparation as assigned. | 05/19/2025 |
| 1210 | Masimo Irvine, CA Engineer, Regulatory & Product Safety B.S. or M.S. in Science or Engineering Exp: 0-2 years |
The Engineer, Regulatory and Product Safety is responsible for providing technical support for all aspects of regulatory and product safety throughout the product realization process. This position will handle projects from product inception, development, through manufacture and customer use. The incumbent provides support to ensure product meets defined safety standards and worldwide regulatory requirements. | 05/19/2025 |
| 1211 | Mattek Ashland, MA Production Associate I Bachelor’s Exp: 1 year |
Participates in duties associated with manufacturing of MatTek tissue models according to SOPs where applicable. May also perform duties assigned under Laboratory Assistant, as needed. | 05/19/2025 |
| 1212 | MMT St. George, UT Applications Engineer I Bachelor’s degree in Engineering or a related field. Exp: 1-3 years |
At MMT, our objective is to develop excellence in automation, machine design, material handling, and custom tooling. Each position contributes to the success of the company through accountability, responsiveness, and a solutions-oriented mindset. We are currently seeking an Applications Engineer to join our dynamic catheter and guidewire manufacturing automation site in St. George, UT. The Applications Engineer’s focus will be post-production machine testing and process development, onsite installations, and rapid prototyping and proof of concept for new opportunities. Additional responsibilities include tooling development support for design engineers, customer technical support, and process report writing | 05/19/2025 |
| 1213 | MMT Angleton, TX Technical Sales Engineer I Bachelor’s in Engineering or equivalent Exp: 1-3 years |
At MMT, our objective is to provide world-class solutions for precision hole making applications and contract medical device manufacturing. Each position contributes to the success of the company through accountability, responsiveness, and a solutions-oriented mindset. Working in concert with the appropriate internal and external resources, the Technical Sales Engineer will primarily focus on being a technical expert across all offerings within SYNEO’s Cutting Tools and Specialty Manufacturing Divisions. This position is required to perform Sample Material Evaluations, Inspections, Data Collection, and give feedback for application specific tooling or Specialty Manufacturing processes. The position requires close collaboration with internal manufacturing stakeholders, engineering, and sales resources to develop and implement recommendations that meet or exceed customer expectations. | 05/19/2025 |
| 1214 | MMT Ramsey, NJ Mechanical Engineer Bachelor’s degree in Mechanical Engineering Exp: 1-3 years |
As a Mechanical Engineer at MMT, you’ll be at the forefront of innovation, designing and testing everything from custom machines to robotics. You’ll collaborate with a talented design team, bring your ideas to life using CAD software, and see your work go from concept to production. | 05/19/2025 |
| 1215 | Medtronic Mounds View, MN Quality Engineer I Bachelor's Degree in Engineering, Science or technical field Exp: 0 years |
The Quality Engineer I will have responsibility for ensuring quality within the Global Calibration Services, Midwest Region (GCSMR) department. GCSMR provides calibrations and support for test and measurement equipment used in facilities, research, development, and manufacturing environments in many business environments in the Midwest and throughout global Medtronic. | 05/19/2025 |
| 1216 | Medtronic Swedesboro, NJ Industrial Engineer Bachelor's Degree Exp: 0 years |
Medtronic is hiring in Woolwich County, here our employees are helping us deliver on the extraordinary. We actively seek a diverse workforce at every level: We require fresh ideas and inclusive insights to maintain our position as an innovative industry leader. That’s why we actively seek, attract, and develop employees who are patient-centric, passionate, and who reflect the wide variety of life experiences found among our patients. | 05/19/2025 |
| 1217 | Medtronic Danvers, MA Quality Engineer II, Manufacturing Operations Master's Degree in engineering/science Exp: 0 years |
We are seeking a Quality Engineer II who is passionate about ensuring product quality and regulatory compliance in support of innovative medical devices. In this role, you’ll contribute to cross-functional efforts and continuous improvement in a dynamic, collaborative environment. In this role you will have responsibility for providing comprehensive manufacturing quality support for commercial medical devices in the area of component manufacturing. This includes activities related to test method validation, process validation, inspection improvements, and process/quality change initiatives. | 05/19/2025 |
| 1218 | Medtronic Tempe, AZ Quality Systems Specialist Master's Degree in engineering/science Exp: 0 years |
In this exciting role as a Quality Systems Specialist – CAPA Specialist supporting the Tempe Campus - you will have responsibility for compliance to the Corrective and Preventive Action (CAPA) processes and Medical Device regulations and requirements, serve as a CAPA subject matter expert; provide guidance to CAPA owners and CAPA Board members to develop CAPA activities and conduct assessment of CAPA documentation. The Quality System CAPA Specialist will ensure compliance with Medtronic policies, FDA regulations, ISO 13485, and other requirements by rigorously assessing CAPA activities and documentation. They will participate in CAPA Board activities, provide guidance and mentorship on CAPA processes and tools, and report on CAPA metrics. Additionally, they will support the development and implementation of CAPA procedures, software, and training, and assist in internal and external audits and inspections. | 05/19/2025 |
| 1219 | Medtronic Mounds View, MN Reliability Engineer I - Cardiac Rhythm Management Bachelor’s degree in Engineering or related field Exp: 0 years |
This Engineer will have the opportunity to support the entire CRM product portfolio through authoring, submission, and maintenance of Periodic Safety Update Reports (PSUR) and other risk management deliverables. This position regularly collaborates with Clinical Evaluation and Regulatory to complete post market surveillance deliverables. This role provides and evaluates the data necessary to support the corrective action (CAPA) and other internal processes (regulatory, clinical, R&D, etc.). This may include support requests for information related to product performance from competent authorities, Medtronic geographies, customers and management. Supports Reliability Engineering with data collection and analysis and regularly communicates product performance data to the organization (via email, product performance meetings and management reviews), or other requests from management. | 05/19/2025 |
| 1220 | Medtronic Minneapolis, MN System Test Engineer II -Neuro Master's degree in Engineering Exp: 0 years |
This position will lead all testing efforts for the Translational Research System team on Neuromodulation & Pelvic Health Implantable products such as cutting-edge neurostimulator systems for Deep Brain Stimulation, Spinal Cord Stimulation, and Sacral Nerve Modulation. The individual will support all test-related phases of development including definition, design, troubleshooting, characterization, and verification of medical device research systems. The individual will be an integral part of the R&T organization delivering the highest quality, life changing technology to our patients. This role requires a strong background in testing, problem solving, and issue investigation with a passion for improving healthcare through technology. | 05/19/2025 |
| 1221 | Medtronic Northridge, CA Quality Engineer II Master's degree in Engineering, Science or technical field Exp: 0+ years |
At Medtronic Diabetes, we are looking for a Quality Engineer II who will have responsibility for providing technical and quality systems expertise within the Operations Quality organization. You will serve as a subject matter expert by providing support for Diabetes commercialized products and projects. Our quality team is looking for talented career engineers to join our organization. We value what makes you unique. Be a part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations. This role will be part of Electronic Technologies and China Operations Quality team. Individuals in this role will provide technical support and quality system expertise for commercialized Diabetes products including Continuous Glucose Monitoring Systems (CGMS) and product accessories. The ideal candidate for this position has a strong technical background and experience in medical device product manufacturing. | 05/19/2025 |
| 1222 | Merck West Point, PA Scientist, Translational Medicine (Hybrid) Master’s degree in Life Sciences Exp: 1+ years |
Translational Medicine is responsible for early clinical development of novel therapeutics, working in close collaboration with Discovery Sciences and late-stage Clinical Research across all therapeutic areas. Our team is focused on innovation and dedicated to translating breakthrough science into innovative medicines that extend and improve the lives of patients worldwide. Through clinical trials, we ensure the safety and efficacy of our pipeline and existing products to produce safe, effective, innovative medicine. | 05/19/2025 |
| 1223 | Meridian Bioscience Memphis, TN Quality Assurance Associate Bachelor’s degree in life science, chemistry, pharmaceutical science, statistics, or health/human services related field Exp: 0-5 years |
The Quality Assurance (QA) Associate will support QA processes, programs, and conduct QA activities. This position will uphold standards, methods, and procedures for all stages of production. This position will identify continuous process improvement areas, in compliance with Good Manufacturing Practices (GMP) and Good Documentation Practices (GLP) processes and documentation for quality control activities. This requires excellent technical skills and abilities, analytical and mathematical skills, organizational and time-management skills, verbal, and written communication skills, plus ability to apply attention to detail. | 05/19/2025 |
| 1224 | Meridian Bioscience Cincinnati, OH Senior Research Associate Master of Science degree Exp: 1 year |
Primary role is to run experiments, acquire and record data, analyze data, draw conclusions for discussion and recommend decisions. | 05/19/2025 |
| 1225 | Mikart Atlanta, GA Quality Control Analyst Chemist Bachelor of Science in Chemistry or in a related science Exp: 0-1 years |
The Quality Control Analyst Chemist for Mikart, LLC is responsible for conducting analyses on various components, in-process materials and finished dosage forms. | 05/19/2025 |
| 1226 | MIMEDX Marietta, GA Associate Product Development Engineer BS/BA in relevant discipline Exp: 0-2 years |
The Associate PD Engineer I will support the operation of the PD group. Candidate will participate in new product development and sustaining engineering activities by following pre-defined protocols and test methods. Some data interpretation will be required. Delegated tasks and procedures are expected to be completed in a thorough and timely manner and communicated to senior PD staff. | 05/19/2025 |
| 1227 | Minaris Allendale, NJ QA Associate II BS degree in a scientifically related field Exp: 1-3 years |
The Quality Assurance Associate plays a pivotal role in ensuring that all quality assurance activities are conducted efficiently and accurately. Under direct supervision, the associate supports daily tasks that are essential for maintaining and improving quality systems and adhering to client-specific procedures. Key responsibilities include document management, review of manufacturing batch records, quality control (QC) data, facilitating material releases, overseeing final product releases, and providing essential assistance to the Quality Management as needed. | 05/19/2025 |
| 1228 | Merck St. Louis, MO Quality Control Associate Scientist Bachelor’s degree in Chemistry, Biochemistry, Biology, or other Life Science discipline Exp: 1+ years |
The Associate Scientist role performs lab testing and supports tasks to assure our product quality meets specifications. | 05/19/2025 |
| 1229 | Merck Sheboygan Falls, WI Associate Quality Control Chemist (Laboratory) Bachelor's Degree in Chemistry, Biochemistry or other Life Science discipline Exp: 1+ years |
The Associate Quality Control Chemist at MilliporeSigma will evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. The QC Chemist is also responsible for the general maintenance and upkeep of the analytical instruments that reside in the QC labs, and assists with managing existing service contracts and the onboarding and retirement of instruments. | 05/19/2025 |
| 1230 | Merck St. Louis, MO Operations Integration Scientist Bachelor's Degree in Chemistry, Biochemistry or other Life Science discipline Exp: 1+ years |
The Operations Integration Scientist is the leading role for the integration and implementation of new custom manufacturing products into the GMP manufacturing facilities. This technically sound position works cross-functionally at multiple manufacturing facilities with Project Management, Quality, Manufacturing, Process and Analytical Development, and customer to efficiently bring new custom/contract manufacturing bioconjugation products into the GMP manufacturing facilities. You manage the technology transfer into GMP by authoring technical documents such as specifications and risk assessments, driving Change Control for new and existing custom manufacturing projects and planning for operational requirements. We’re looking for a candidate with strong technical skills, demonstrated ability to work within a cross- functional team, and excellent interpersonal and team building skills. The position will be based in St. Louis, Missouri. | 05/19/2025 |
| 1231 | Merck St. Louis, MO Associate Production Scientist Bachelor’s degree in Biochemistry, Biology or other Scientific discipline. Exp: 1+ years |
The Associate Production Scientist role is focused on creating manufactured kits of reagents to support Multiplex, ELISA, and RIA kits in the Immunoassay Platform Solutions (IPS) portfolio in a timely manner. | 05/19/2025 |
| 1232 | Merck St. Louis, MO Associate Scientist - Manufacturing Histology Bachelor's degree in Chemistry, Biochemistry, Biology, or other Life Science discipline Exp: 1+ years |
Under moderate supervision, the Associate Scientist – Mfg Histology performs slide manufacturing, H&E staining, IHC staining, and other laboratory operations in Manufacturing associated with slide manufacturing and block qualification according to standard operating procedures (SOPs) and regulatory requirements; assists with document updates as necessary. | 05/19/2025 |
| 1233 | Merck St. Louis, MO Manufacturing Compliance Specialist Bachelor’s Degree in Chemistry, Biochemistry, Biology, or other Life Sciences or Engineering discipline Exp: 1+ years |
MilliporeSigma in St. Louis, MO is seeking a Manufacturing Compliance Specialist for the Ewing Facility in St. Louis, MO. This Compliance Specialist will be responsible for supporting the Ewing operations through the management of quality records (deviations and CAPAs), managing the creation and updates of operating procedures, and assisting label issuance/management for production. This role will work collaboratively with QA, QC, Operations, Engineering, Validation, Process Development and Maintenance while adhering to GMP principles. | 05/19/2025 |
| 1234 | Merck St. Louis, MO Quality Assurance Product Release Specialist Bachelor’s Degree in a scientific (Biology, Chemistry, etc.) or engineering discipline (Chemical, Mechanical, etc.) Exp: 1+ year |
The Quality Assurance Product Release Specialist plays a critical role in ensuring the timely and compliant release of purchased and produced goods at MilliporeSigma. This position is responsible for performing a variety of quality review functions according to established criteria and guaranteeing that products meet all necessary specifications and regulatory requirements. The Quality Product Release Specialist will collaborate with various internal stakeholders and will be a subject matter expert in QA product release processes. | 05/19/2025 |
| 1235 | Modulo Bio San Diego, CA Stem Cell Scientist MS in Genetics, Molecular Biology, Developmental Biology, Biochemistry, Regenerative Medicine, Neuroscience, or related field Exp: 1+ years |
Modulo Bio is seeking a Stem Cell Scientist to develop and scale an induced-pluripotent stem cell (iPSC)-based in vitro model of the neuroimmune system. Modulo Bio is building a proprietary immune cell modeling platform, which incorporates human genetics, functional genomics, molecular biology, cellular and tissue profiling, disease model engineering, and advanced computational models. The successful candidate will build a complex cell model platform with the goal of improving our understanding of human biology and therapeutic interventions to inform early and late stage pipeline efforts. Candidates with an eagerness to work within a highly leveraged, team-driven, dynamic research environment will be prioritized. The candidate will work in close collaboration with our internal Computational Biology group which is focused on next-generation sequencing (NGS), functional genomics, cell or tissue profiling, and bioinformatics analyses of cutting-edge large-scale genetic screening or single-cell technologies to enhance our analytic capabilities and to reveal the underlying mechanisms of human disease. | 05/19/2025 |
| 1236 | Moog Murphy, NC Manufacturing Engineer Bachelor's degree in Engineering/Engineering Technology or equivalent Exp: 1 year |
Our team in Moog Industrial Group is looking for a Manufacturing Engineer to join them. You will report to the Site Manager and will have an onsite work schedule in Murphy, North Carolina. | 05/19/2025 |
| 1237 | Novartis Durham, NC Bioprocess Engineer I Bachelor of Science Degree in Biology, Chemistry, Biotechnology or applicable field Exp: 1-2 years |
The Bioprocess Engineer I is responsible for executing assigned manufacturing tasks and activities according to the production schedule to ensure timely production of products that meet quality standards in compliance with relevant GMP, safety, and environmental guidelines. The role level will be determined by the years of relevant experience. The role is located on-site in our Durham, NC location. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. | 05/19/2025 |
| 1238 | Novartis Millburn, NJ Production Technician I Bachelor’s degree in relevant Engineering or Scientific discipline is highly preferred Exp: 1+ years |
Production Technicians play an active role in daily production of Radioligand Therapies (RLT) as well as setup and preparation of instruments and equipment. The Production Technician adheres to regulatory requirements while performing job functions, executing production as per batch records and SOPs. Responsibilities are performed within a team and according to an assigned production shift schedule. The Production Technician works closely with the Manager and Lead to ensure production is executed in a safe and timely manner. | 05/19/2025 |
| 1239 | Novartis Indianapolis, IN Production Technician I Bachelor’s degree in relevant Engineering or Scientific discipline is highly preferred Exp: 1+ years |
Production Technicians play an active role in daily production of Radioligand Therapies (RLT) as well as setup and preparation of instruments and equipment. The Production Technician adheres to regulatory requirements while performing job functions, executing production as per batch records and SOPs. Responsibilities are performed within a team and according to an assigned production shift schedule. The Production Technician works closely with the Manager and Lead to ensure production is executed in a safe and timely manner. | 05/19/2025 |
| 1240 | Novartis Indianapolis, IN QC Technician Bachelor’s degree in microbiology, chemistry or a related field Exp: 1 year |
We are seeking a highly motivated and detail-oriented Quality Control (QC) Technician to support both Microbiology and Chemistry functions at our We are seeking a highly motivated and detail-oriented Quality Control (QC) Technician to support both Microbiology and Chemistry functions at our radioisotope production site. The primary responsibility of this role will be to perform routine quality control testing and analytical functions to ensure the production of high-quality radioisotopes. The QC Technician will work closely with the Quality Control and Production teams to maintain regulatory compliance, meet GMP (Good Manufacturing Practices) standards, and ensure the safety and efficacy of products produced at our Indianapolis Isotopes facility. | 05/19/2025 |
| 1241 | Novartis Morris Plains, NJ Manufacturing Operations Specialist Bachelor’s degree Exp: 1 year |
The Manufacturing Operations Specialist is responsible for the dispensary / ISO8 area tasks including kitting and material flow, inventory management and other duties required to support the core functions. | 05/19/2025 |
| 1242 | Natera San Carlos, CA Clinical Lab Associate BS/BA in a biological science or similar field of study Exp: 0-2 years |
Natera is currently seeking a Clinical Laboratory Associate to analyze laboratory specimens following the standard methods and procedures while maintaining equipment and instruments in good operating condition by troubleshooting malfunctions as needed. | 05/19/2025 |
| 1243 | Natera Austin, TX Clinical Lab Operator Horizon BS/BA in a biological science or similar field of study Exp: 0-2 years |
Assists in analyzing specimens and maintains equipment in good operating condition. | 05/19/2025 |
| 1244 | Natera Austin, TX Clinical Lab Operator I BS/BA in a biological science or similar field of study Exp: 0-2 years |
Assists in analyzing specimens and maintains equipment in good operating condition. | 05/19/2025 |
| 1245 | KARL STORZ Goleta, CA Design Verification Test Engineer II MS degree in Electronics Technology/Engineering or related field Exp: 0-3 years |
We're looking for a talented Design Verification Engineer to join our team! As a key player in ensuring our products meet the highest quality standards, you'll design and execute verification procedures, troubleshoot issues, and train other test engineers. If you're passionate about delivering exceptional results and collaborating with top-notch professionals, we want to hear from you! | 05/12/2025 |
| 1246 | KBI Biopharma Durham, NC Manufacturing Specialist I Master’s degree in a related scientific or engineering discipline Exp: 0+ years |
Responsible for leading technical support activities for GMP Manufacturing Operations in a multi-product, large scale biopharmaceutical facility. This role will support, but not limited to the following: Drafting, routing, and revision of manufacturing batch records, support records, and standard procedures. First line of defense for manufacturing events. Individual will assess, provide, and help implement immediate corrective and preventative actions. Provide manufacturing process support during on-going shop floor execution as needed. Support new equipment enrollment workflow from purchasing to qualification as needed. SME support on critical laboratory equipment supporting manufacturing operations. Additionally, SME will lead and manage all activities and event related to critical laboratory equipment. Support safety initiatives, compliance, and quality requirements. | 05/12/2025 |
| 1247 | KBI Biopharma Durham, NC Manufacturing Associate I (Night Shift) Bachelor’s degree in a related scientific or engineering discipline Exp: 0-2 years |
The Manufacturing Associate I/II is responsible for the execution of Upstream or Downstream production activities for early and late-phase Cell Culture programs within a GMP environment. The Manufacturing Associate I/II must follow the instructions depicted in SR’s, EPR’s, BR’s, SOP’s and forms. Additionally, must ensure all work is conducted following Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and Good Laboratory Practices (GLP); including ‘Right the First Time’ (RFT). The candidate will maintain a sense of ownership of the production processes, manufacturing environment and facility. They will be exposed to various unit operations including media/buffer preparation, shake flask operations, seed expansion, bioreactor setup and operations, cell culture harvest setup and operations, aseptic technique, chromatography, ultrafiltration, and drug substance filling operations; as well as to analytical tools and general biotechnology auxiliary equipment (pumps, sterile tubing welders and sealers, pH/Conductivity/osmolality meters). Following task execution, the Manufacturing Associate I/II will review the executed production records (SR’s, ERP, and BR’s) to ensure GxP compliance. | 05/12/2025 |
| 1248 | KBI Biopharma Durham, NC Validation Engineer I Bachelor’s degree in Chemical Engineering, Industrial Engineering, Biomolecular Engineering, Mechanical Engineering, or related scientific field. Exp: 1-3 years |
The Validation Engineer I/II will be responsible for facilitating the validation lifecycle process for the Validation Department to ensure all equipment and systems are in a qualified state suitable for the intended use. This may entail, assisting with the planning, development, project management, and execution of life cycle engineering and validation lifecycle documentation elements of engineering and validation lifecycle design, commissioning, maintenance, qualification, and the interfaces with quality system lifecycle compliance requirements. This position will provide support for more than one area of subject matter expertise for validation disciplines which may include: Facilities qualification, Utilities qualification, Equipment qualification, Manufacturing process control system qualification and Cleaning validation. | 05/12/2025 |
| 1249 | KBI Biopharma Boulder, CO Manufacturing Associate I (Night Shift) Bachelor’s degree Exp: 0-5 years |
Coordinate and perform cGMP manufacturing operations for manufacturing biopharmaceutical products. Ensure the effective use of material, equipment, and personnel while making products at high-quality levels. | 05/12/2025 |
| 1250 | KBI Biopharma Durham, NC Manufacturing Specialist I Master’s degree in a related scientific or engineering discipline Exp: 0+ years |
Responsible for leading technical support activities for GMP Manufacturing Operations in a multi-product, large scale biopharmaceutical facility. This role will support, but not limited to the following: Drafting, routing, and revision of manufacturing batch records, support records, and standard procedures. First line of defense for manufacturing events. Individual will assess, provide, and help implement immediate corrective and preventative actions. Provide manufacturing process support during on-going shop floor execution as needed. Support new equipment enrollment workflow from purchasing to qualification as needed. SME support on critical laboratory equipment supporting manufacturing operations. Additionally, SME will lead and manage all activities and event related to critical laboratory equipment. Support safety initiatives, compliance, and quality requirements. | 05/12/2025 |
| 1251 | KBI Biopharma Louisville, CO Research Associate I Bachelor’s degree in a scientific discipline Exp: 0-2 years |
Join an analytical team in a dynamic work environment where you will participate in contracted client analytical programs as a member of the Characterization Services team. The individual in this position will support product characterization studies of biopharmaceutical products through executing experimental protocols, performing data analysis, documenting work in technical reports, and presenting results to clients and management. Bioanalytical testing may include (but not limited to) HPLC, electrophoresis, mass spectrometry, and biophysical techniques. Required to work in teams to solve scientific problems, and to train and be trained by colleagues. | 05/12/2025 |
| 1252 | KBI Biopharma Durham, NC Research Associate I Bachelor’s or Master's degree in chemistry, biochemistry or related area (or equivalent training) Exp: 0+ years |
Join a highly technical analytical team in a dynamic work environment where you will participate in contracted client analytical programs as a member of the Analytical and Formulation Sciences (AFS) Department. The individual in this position will be responsible for executing experimental protocols and performing data analysis in biopharmaceutical laboratories. | 05/12/2025 |
| 1253 | Kindeva Union City, CA Analytical Scientist BS in Chemistry or in a pharmaceutical related discipline. Exp: 1+ years |
Analytical Scientist required to support multiple R&D activities in Union City. This is a key role within an expanding team of formulation and product development scientists and offers the successful candidate an opportunity to make a significant contribution to the development of new inhalation products and future technologies by applying their creative technical skills and using their scientific experience. We develop drugs including proteins peptides, other biologic compounds as well as small molecules. | 05/12/2025 |
| 1254 | Kindeva Lexington, KY QC Microbiologist - Third Shift BA/BS degree in Chemistry, Biology, Microbiology, or related field Exp: Entry Level |
As a Microbiologist I, you will play an essential role in protecting product quality and ensuring a contamination-free environment. Your daily work will directly support the safety and reliability of our pharmaceutical products through environmental monitoring and microbiological testing. By mastering aseptic techniques and partnering closely with experienced professionals, you will help maintain high laboratory standards, ensure regulatory compliance, and build a strong foundation in microbiological quality control. Your attention to detail and commitment to excellence will contribute to patient safety and support our mission to deliver life-changing therapies with integrity and care. | 05/12/2025 |
| 1255 | Kindeva Bridgeton, MO Quality Engineer Master's degree in a scientific or engineering discipline Exp: 1-3 years |
In this role, you will develop, direct, and lead Quality oversight for process improvements in equipment and material preparation, aseptic compounding, filling, inspection, and packaging at the Brentwood, Maryland Heights, and Bridgeton facilities. You will coordinate support activities, reviews, audits, and the release of semi-finished products and components to align with site-wide objectives. You will collaborate with cross-functional teams to support continuous improvement initiatives, incident investigations, and change management. Additionally, you will make decisions related to Incident Investigations and Corrective and Preventive Actions, ensuring a focus on overall quality, site priorities, and operational success. | 05/12/2025 |
| 1256 | Kite Santa Monica, CA Sr. Research Associate - Viral Vector Upstream MS/MA in Chemical/Biochemical Engineering, Biochemistry, Biology or related field Exp: 0+ years |
Kite Pharma is seeking a creative and highly motivated Sr. Research Associate to join our growing vector process design team in Santa Monica. In this integral role, you will contribute to the company's pipeline development for hematopoietic and solid tumor malignancies by supporting the development, scale-up, process characterization, and technology transfer of the lentiviral vector process. | 05/12/2025 |
| 1257 | Krystal Moon Township, PA Bioprocess Engineer Bachelor’s degree, preferably in life sciences Exp: 1+ years |
Krystal Biotech, Inc is seeking a highly motivated and dynamic Bioprocess Engineer to support our product manufacturing at our Pittsburgh GMP facility. This role is critical to our make a meaningful difference in the lives of underserved patient populations having rare diseases. Quality, safety and on-time delivery is a must to be successful in this role! The ideal candidate will have foundational experience in upstream and/or downstream biologics or gene therapy manufacturing. | 05/12/2025 |
| 1258 | Krystal Pittsburgh, PA Bioprocess Engineer Bachelor’s degree, preferably in life sciences Exp: 1+ years |
Krystal Biotech, Inc is seeking a highly motivated and dynamic Bioprocess Engineer to support our product manufacturing at our Pittsburgh GMP facility. This role is critical to our make a meaningful difference in the lives of underserved patient populations having rare diseases. Quality, safety and on-time delivery is a must to be successful in this role! The ideal candidate will have foundational experience in upstream and/or downstream biologics or gene therapy manufacturing. | 05/12/2025 |
| 1259 | Krystal Pittsburgh, PA Research Associate, Analytical Sciences and Clinical Testing Services Bachelor’s degree (Biology, Biochemistry, Chemistry, or related science) Exp: 0-3+ years |
Krystal Biotech, Inc is seeking a highly motivated Research Associate, Analytical Sciences and Clinical Testing Services to perform high quality analytical testing in support of Krystal’s process development, product development, and clinical sample analysis efforts. This position will be laboratory based, Monday-Friday standard hours. | 05/12/2025 |
| 1260 | Krystal Pittsburgh, PA Clinical Trial Associate/Clinical Research Coordinator BS/BA degree required in science/health-related field. Exp: 1-3 years |
Krystal Biotech, Inc. is seeking a Clinical Trial Associate to support our Clinical Operations Team. The Associate's responsibilities will entail, but not be limited to, assisting with the management and inventory of clinical supplies, ensuring proper materials are available at clinical sites in a timely manner, and working with the Clinical Operations team to support multiple Clinical Trials. Conducting reviews of trial data and follow GCP/ICH protocols/guidelines. Will require travel to Clinical sites, including up to 50% of the time, during peak periods. | 05/12/2025 |
| 1261 | Krystal Pittsburgh, PA Process Validation Associate Bachelors’ Degree in Chemical Engineering, Biomedical Engineering, or related Exp: 1+ year |
Krystal Biotech is seeking a highly motivated Process Validation Associate (1+ years’ experience) or Engineer (3+ years’ experience) to support process validation planning, design, and execution. This person will be responsible for risk assessments, process improvements, investigations, and other projects. They will also play a pivotal role in technology transfer and ensuring processes transition properly from site to site. | 05/12/2025 |
| 1262 | Kyowa Kirin Sanford, NC Project Automation Engineer Bachelor’s degree in Engineering Exp: 1 year |
A project automation engineer to assist in design and start-up of a new manufacturing facility. The project automation engineer will work directly with the Site Head during the project phases and then transition to an operational role in the plant. The Automation Engineer is responsible for the design, commissioning, and operation of key KKNA Manufacturing Facility automated systems. | 05/12/2025 |
| 1263 | LabConnect Cleveland, OH Clinical Sample Specialist Bachelor’s degree Exp: 6 months |
The Clinical Sample Specialist is responsible for biospecimen management activities for samples arriving at the LabConnect Cleveland facility. The Specialist will perform tasks in support of receiving specimens for storage, onsite processing, distribution to biorepository, and shipments to partner laboratories or other facilities. Additional activities include maintenance of specimen storage equipment, monitoring accessioning and biorepository consumables, and the organization of departmental SharePoint documentation. The Specialist will regularly communicate across departments and interact with project management, facilities, data management, and IT. | 05/12/2025 |
| 1264 | LG Chem Evansville, IN Associate Chemist Bachelor’s Degree in Chemistry or Related Scientific Field Exp: 1+ years |
The Associate Chemist is responsible for analytical, environmental and physical testing He or she also performs testing on raw materials and compounded products. This person will also participate in the development and formulation of new products under the direction of a Chemist or Senior Chemist. The Associate Chemist may provide any necessary technical support to various other departments. In addition, he or she is responsible for any other task the Chief Technology Officer deems necessary. | 05/12/2025 |
| 1265 | LGC Clinical Diagnostics Cumberland Foreside, ME Manufacturing Chemist I Bachelors degree in life science field or other related science or medical curriculum Exp: No exp |
The Manufacturing Chemist I fulfills the essential role of preparing reagents, buffers, stocks, and other solutions using established procedures within the operations laboratory. They will use general laboratory equipment and techniques to perform these tasks under both direct and indirect supervision. They are expected to perform routine analysis and interpretation of test results against established acceptance criteria with limited judgment. | 05/12/2025 |
| 1266 | LGM Pharma Rosenberg, TX Quality Assurance Specialist Bachelor’s degree in a scientific discipline Exp: 1+ years |
Performs initial, in-process and final inspections during manufacturing/packaging of product; resolves inspection findings with Packaging Manager and /or QA Manager. Collects product samples for product release testing, process validation testing and product stability as applicable and prepare labels at completion of packaging. Prepares documentation and forward samples to QC Lab for required testing; records information on batches in-process of testing on QC board; notifying QC of any urgent testing. Monitors incoming materials as received in Quarantine. Reviews material received paperwork and compare to material received for accuracy; notifying Materials Department to call supplier if CofA has not been received or CofA is incomplete. Coordinates with production areas to anticipate material usage to meet required schedule. Performs other related duties as required. | 05/12/2025 |
| 1267 | Liquidia Morrisville, NC Quality Control Associate Scientist B.S. degree in chemistry, pharmaceutical sciences, or a similar scientific field Exp: 0-2 years |
We are looking for an Associate Scientist, Quality Control. In this “hands-on” role within the Quality Control Lab, the Associate Scientist will join a talented and collaborative team that welcomes input and suggestions to help continue Liquidia’s upward trajectory at the most exciting time in the Company’s history. Critical to success are a scientific laboratory background, ability to follow CGMP documentation requirements, and excellent communication skills. The Associate Scientist will conduct laboratory analysis of raw materials and intermediates in support of Liquidia’s lead product candidate. | 05/12/2025 |
| 1268 | Liquidia Morrisville, NC Manufacturing Technician B.S. degree in chemistry, pharmaceutical sciences, or a similar scientific field Exp: 0-2 years |
We are looking for a hands-on and experienced Manufacturing Technician. In this role, you will perform routine running of manufacturing equipment to support production and R&D efforts. Furthermore, you will provide feedback to engineering and scientific staff on process performance and ideas for process improvement. | 05/12/2025 |
| 1269 | Lonza Portsmouth, NH Manufacturing Associate I (Nights) BS in a Science related field Exp: 0-4 years |
Join Lonza as a Manufacturing Associate Level I for a remarkable chance to contribute to producing therapeutic proteins in New Hampshire, USA. Work with a top team to implement innovative ideas for improving lives under cGMP conditions! Working nights from 7pm-7am on a rotational schedule. | 05/12/2025 |
| 1270 | Lonza Houston, TX QC Investigator II Bachelor’s degree in a scientific subject area or related field. Exp: 0-4 years |
At Lonza AG, we are driven by the ambition to deliver best-in-class healthcare solutions. Our QC Investigator II role is an outstanding opportunity to join a team that flourishes with innovation and quality. This position is based in Houston, TX, and is vital to our mission of achieving detailed results by closely adhering to quality standards. Your confirmed ability to efficiently implement corrective actions and lead continuous improvement initiatives will be the cornerstone of your success with us! | 05/12/2025 |
| 1271 | Lonza Greenwood, SC Lab Technician Bachelor’s degree or equivalent experience in a scientific field (e.g., Biology, Chemistry, Food Science, Nutrition, or related subject area) Exp: 1+ years |
Become an essential part of a world-class team at Lonza AG as a Lab Technician in Greenwood, SC, USA! This outstanding opportunity allows you to support critical R&D functions, formulation development, and testing. Join us in our ambitious mission to improve lives through science. | 05/12/2025 |
| 1272 | Lotte Biologics Syracuse, NY Associate Scientist, Upstream Process Development M.Sc./M.Eng degree Exp: 0-2 years |
The primary role of the Associate Scientist, Upstream Process Development is to execute laboratory experiments in the development, optimization, characterization, and scale-up of biologics upstream cell culture processes from laboratory to manufacturing scale using knowledge of cell culture, cell banking, medium preparation, bioreactor production, and primary recovery. The role is a combination of laboratory- and office-based work. This role will execute and document laboratory studies in laboratory notebooks. Additionally, this role will support documentation review, protocols, technical reports, change controls, and CMC regulatory submissions under supervision. The Associate Scientist is expected to follow detailed GLP/GMP procedures and safety requirements. This role will work in a team environment and will interact with other functional departments. Additionally, this position is a team-based position that may require work on evenings, weekends, and holidays | 05/12/2025 |
| 1273 | Lotte Biologics Syracuse, NY Assistant Scientist, Quality Control BS degree in scientific area Exp: 0-3 years |
The role of Assistant Scientist within our Quality Control Release department conducts routine general chemical and/or biological testing of materials and products for in-process, release and stability purposes, in compliance with all applicable procedures and regulations. A variety of duties are performed relating to the efficient and effective functioning of the Quality Control lab. | 05/12/2025 |
| 1274 | Lilly Pleasant Prairie, WI Process Engineer Bachelors Degree in Engineering Exp: 1+ years |
Engineer - Process is responsible for establishing and maintaining the reliable operation and qualified state of the equipment and business processes in the area that they support. Ensure that equipment is in-control, compliant, and capable of meeting customer needs, while also driving associated continuous improvement effort. | 05/12/2025 |
| 1275 | Lilly Lebanon, IN Process Engineer - Lilly Medicine Foundry BS or MS in chemical engineering or related discipline Exp: 1-4 years |
We are seeking a Process Engineer to support the pilot plant facility in Lebanon with a focus on peptide and oligonucleotide synthesis. This position involves solving technical challenges with equipment design, developing and sustaining process knowledge, optimizing processes, and managing equipment capabilities. | 05/12/2025 |
| 1276 | Lilly Lebanon, IN Automation Engineer, Drug Substance - Design & Delivery, Lilly Medicine Foundry Bachelor of Science Degree in engineering or a related science field Exp: 1 year |
The Engineer – Automation - Drug Substance Design / Delivery role requires a 4-year engineering degree, preferably in Chemical, Mechanical, Electrical Engineering, or related science field. The position requires high learning agility and a background in DCS programming (preferably DeltaV) and experience in automated API manufacturing or related processes. This role will initially be in support of the design and delivery phase of the project, as part of the Global Process Automation & Control Engineering (GPACE) team. As the site nears completion and start-up activities begin, this role will transition into a Lebanon Site role for long term operational support. GPACE is part of Lilly’s Corporate Engineering Tech Center (ETC). GPACE provides automation, measurement, and process control solutions, and is a technical resource for training, standards, capital project delivery, and Lilly’s standard automation platforms. GPACE’s primary customers are global manufacturing and development sites, Manufacturing Information Technology, and peer groups such as Global Facilities Delivery (GFD). | 05/12/2025 |
| 1277 | Lilly Lebanon, IN Manufacturing Associate - Advanced Manufacturing Bachelor''s degree in STEM field Exp: 1+ years |
The Manufacturing Associate will be responsible for performing routine manufacturing activities across GMP manufacturing areas, including: Cell Culture, Downstream Purification, and Fill & Finish at the Lebanon Advanced Therapies, LP2 site. Initially, the Manufacturing Associate will be responsible for supporting execution of equipment qualification, developing site operations procedures and setting up production areas. During this initial project delivery/startup phase of the project, roles will be fluid and dynamic. Once the plant is operational, the Manufacturing Associate will be responsible for execution of production activities on their shift under the leadership of the shift supervisor. | 05/12/2025 |
| 1278 | Lilly Lebanon, IN Sterility Assurance Scientist - Advanced Therapies Manufacturing Bachelors in Microbiology, Biology, Biochemistry, Biochemical Engineering, Chemical Engineering, or other related scientific discipline Exp: 1+ years |
Sterility Assurance – Technical Services/Manufacturing Scientist (TS/MS) role is a technical position that develops and implements the site’s sterility assurance related initiatives and provides technical leadership with regard to sterility assurance & environmental monitoring strategies. Primary objectives include the start-up and compliant manufacturing of gene therapy drug product and drug substance, particularly as it relates to development and implementation of sterility assurance strategies, including environmental monitoring, aseptic process simulations, facility cleaning, facility sanitization, and sterility assurance risk management. | 05/12/2025 |
| 1279 | Lilly Indianapolis, IN Scientist – API Manufacturing Process Support Master's Degree in STEM Discipline Exp: 1 year |
The Manufacturing Scientist provides the technical support required to achieve the reliable and compliant manufacture of the Active Pharmaceutical Ingredient External Manufacturing (API EM) portfolio which includes raw materials, intermediates, enzymes and bulk drug substances. The API EM Manufacturing Scientist executes technical projects (experimental, modeling and/or production data analysis) to improve and optimize process control, yield, purity, and/or productivity. In addition, the manufacturing scientist should be capable and technically independent in setting up and executing a variety of experiments at the laboratory scale and conduct research on manufactured product for process improvements and troubleshooting in the technical services and manufacturing sciences laboratory. | 05/12/2025 |
| 1280 | Lilly Indianapolis, IN Chemist - Oligonucleotide Chemistry Bachelors and/or Masters in Chemistry or related scientific field Exp: 1+ years |
The Lilly Genetic Medicines Team is looking for a collaborative, creative and energetic problem solver to join a multidisciplinary team at the front edge of innovation. You will join our fast-paced, interdisciplinary team as we utilize novel RNA/oligonucleotide based therapeutic modalities to enhance the Lilly portfolio. The successful applicant will utilize their knowledge and technical expertise to accelerate the core capabilities and development of internal RNAi-based clinical candidates. | 05/12/2025 |
| 1281 | Lumen Bioscience Seattle, WA Manufacturing Compliance Associate Bachelor's degree in a relevant scientific discipline Exp: 1-2 years |
Lumen Bioscience is seeking a detail-oriented Manufacturing Compliance Associate to support our GMP operations and ensure compliance within our pharmaceutical manufacturing environment. This role involves conducting thorough investigations of manufacturing deviations, identifying root causes, and implementing effective corrective and preventive actions. If you have a passion for quality, strong technical writing skills, and enjoy collaborating across teams, we encourage you to apply. | 05/12/2025 |
| 1282 | Lumos Remote, Quality and Compliance Specialiss Bachelor's Degree ( four year college or technical school) Required, Field of Study: Biology, Chemistry, or related technical discipline Exp: 1-3 years |
Join us in our pursuit to make a difference. Together, we can change the future of medicine! This position reports to the Vice President, Quality and Compliance and is responsible for providing quality support of product development and clinical trial activities and associated functions performed by external contract research, development and manufacturing organizations. This position also supports internal quality systems and compliance functions. The Quality and Compliance Specialist is expected to execute established processes involving quality assurance, quality systems and compliance. | 05/12/2025 |
| 1283 | RoslinCT Hopkinton, MA QC Analyst II, Microbiology 3rd Shift Bachelor's Degree in scientific discipline, Microbiology focus Exp: 0-7+ years |
The Quality Control Microbiology, QC Analyst will be responsible for collecting environmental samples in clean room areas to support manufacturing operations, sample management activities, and testing of cell therapy in-process and release product samples. The person will be responsible for reporting data and writing/revising standard operating procedures (SOPs) and test methods. This position will also provide support to assist the QC group and partner project teams during technology transfer, analytical method qualification, and routine GMP testing. The QC Analyst I/II, Microbiology will partner with the QC analytical team, interface with multiple groups including manufacturing, and must have the ability to assess method suitability, interpret results, perform tasks independently, and troubleshoot. Identifies and supports initiation and completion of deviations, corrective and preventative actions, and laboratory investigations in compliance with all applicable quality systems and current cGMPs. | 05/12/2025 |
| 1284 | RoslinCT Hopkinton, MA QC Analyst I/II, Analytical 3rd shift Bachelor's Degree in scientific discipline, Microbiology focus Exp: 0-5+ years |
The Quality Control Analytical, QC Analyst will be executing analytical methods such as appearance, pH, osmolality, cell counting, ELISAs, flow cytometry and related methods. This position will also provide support to assist the QC group and partner project teams during technology transfer, analytical method qualification, and routine GMP testing. The QC Analyst I/II, Analytical will partner with the analytical team, interface with multiple groups, and must have the ability to assess method suitability, interpret results, perform tasks independently, and troubleshoot. He/she will be responsible for authoring Standard Operating Procedures (SOPs), specifications and Test Methods. He/she will assist in the implementation of new assay methodologies and the associated instrumentation. Identifies and supports initiation and completion of deviations, corrective and preventative actions, and laboratory investigations in compliance with all applicable quality systems and current cGMPs. | 05/12/2025 |
| 1285 | Illumina San Diego, CA Packaging Engineer Bachelor’s degree Exp: 0-2 years |
Develops new packaging or containers to meet established requirements and maintains oversight and quality of existing packages/containers for all product groups. Defines package requirements for product groups and customer requirements. Develops recommendations according to the nature of the product, cost limitations, legal requirements, and the type of protection required, taking into consideration the need for resistance to external variables. May be responsible for coordination of activities and logistics at secondary contract packaging and labeling sites. Responsibilities may include documentation management and an understanding of good manufacturing practices (GMPs). Uses appropriate tools and performs integrity analysis of packaging and improves manufacturing techniques. | 05/04/2025 |
| 1286 | Illumina San Diego, CA Facilities Engineer 1 Bachelor’s or Master's Degree in Engineering, Mechanical Engineering, Electrical Engineering Exp: 0-2 years |
The Facilities Engineer 1 will be responsible for developing and executing validation protocols as related to new or upgraded facilities and utilities as used for medical device manufacturing. This person will work cross-functionally to assist with the development of requirements based on their expertise in clean rooms, water systems, HVAC and other systems used to support a regulated manufacturing environment. This person will also be responsible for report writing. | 05/04/2025 |
| 1287 | Illumina San Diego, CA Scientist 1 Bachelor’s degree Exp: 0-2 years |
We are looking for an enthusiastic and motivated individual for this Scientist 1 position within the Core Services Library Prep Lab to help run day to day operations. Our ideal candidate will work cross functionally with the team and other groups sharing and using their knowledge of molecular biology, Next Generation Sequencing libraries and Illumina library prep and liquid handler automation. | 05/04/2025 |
| 1288 | ImmunityBio El Segundo, CA Clinical Trials Associate Bachelor’s degree Exp: 0-2 years |
Responsible for clinical trials administration to ensure the most effective and efficient conduct of clinical research studies. | 05/04/2025 |
| 1289 | Imricor Burnsville, MN Quality Assurance Engineer Bachelor of science in engineering, science, or technical field Exp: 0-2+ years |
This Quality Engineer position will be responsible for sustaining existing medical device manufacturing lines for heart ablation catheters and associated capital equipment. The Quality Engineer implements, maintains and enforces the internal quality management system to meet ISO standards and FDA quality system regulations. This position develops and implements inspection/validation processes necessary to verify products meet requirements. This position works closely with manufacturing, regulatory, and development to establish/ensure compliance with the quality system throughout the product lifecycle. | 05/04/2025 |
| 1290 | Indivior Raleigh, NC MQA Specialist (2nd Shift) Bachelor’s degree in science, engineering field Exp: 1-3 years |
The Manufacturing Quality Assurance (MQA) Specialist is responsible for providing quality oversight to all manufacturing areas to ensure product quality and SOP/GMP compliance. The MQA Specialist will work closely with production personnel to complete in-process batch record review, resolve batch related issues, and ensure proper good documentation practices. In addition, the MQA Specialist will be responsible for performing routine environmental monitoring to assess the viable and nonviable particulate levels within classified manufacturing rooms and support rooms. | 05/04/2025 |
| 1291 | Insmed Lebanon, NH Research Associate Bachelor’s degree in biology or related field Exp: 0-2 years |
We are seeking a highly motivated Research Associate to support discovery and development campaigns focused on next-generation biotherapies for serious and unmet medical needs. The candidate will work within the immunology team, conducting in vitro, ex vivo, and in vivo immunoassays on a diverse array of biological drug candidates. | 05/04/2025 |
| 1292 | Insmed Bridgewater, NJ QA Product Quality Complaint Specialis BS in engineering, Life Science or related subject area Exp: 1-2 years |
Overview: Reporting to the Director, Product Quality Complaints, the Product Quality Complaint Associate, QA will play a key role in the complaint process. Specific areas of responsibility include ensuring accurate and thorough complaint intake information, assessing product replacement needs, troubleshooting issues with patients, including on phone support, conducting patient follow ups, supporting product complaint investigations, and tracking and trending complaint data. This position is based in our Bridgewater, NJ HQ (onsite 3 days a week). | 05/04/2025 |
| 1293 | Insmed Lebanon, NH Associate Scientist, Bioinformatics BS in Bioinformatics, Quantitative Biomedical Sciences, Computer Science, Statistics, Mathematics, or a related Exp: 1+ years |
The candidate will be a core member of a computational team developing and applying cutting-edge AI-driven protein engineering methods to design next-generation biotherapeutics, and will work closely with a dynamic and multidisciplinary team conducting associated protein engineering and preclinical analysis experiments. In particular, the role focuses on analysis and modeling of data collected as part of our diverse biotherapeutic development campaigns, with an initial primary focus on data from immunoassays including immunopeptidomics and T cell activation. The candidate will have the opportunity to build and use bioinformatics tools and pipelines to extract information from these rich datasets and thereby help guide design and engineering of life-altering innovative biotherapeutic agents. | 05/04/2025 |
| 1294 | Integer Alden, NY Engineer I Bachelor’s degree in an engineering or related technical field Exp: 0-3 years |
The primary purpose of this position is to perform work which involves general engineering methods and tools. As an entry level engineer, you will ensure that Integer’s internal and external customer expectations are met or exceeded with the direction, instruction and guidance from more experienced engineers and managers in your organization. | 05/04/2025 |
| 1295 | Integer Plymouth, MN Lead R&D Technician Bachelor’s degree Exp: 0-3 years |
The primary purpose of this job is to perform non-routine assignments and provide technical support with a high variety and complexity. Develops, designs, installs, and maintains new processes, tests, and/or control systems. Has critical company knowledge of processes/systems and is responsible for projects and deadlines. Acts as a lead technician in a group. | 05/04/2025 |
| 1296 | Integra LifeSciences Plainsboro, NJ Microbiology Technician I Bachelor’s degree, in Microbiology or Biology Exp: 0-3 years |
The Microbiologist I will provide support to the QC Microbiology Laboratory as pertaining to the respective responsibilities. Performs functions such as executing laboratory testing for in-process and finished good products, water, stability studies, and validation studies as well as performs environmental monitoring. This position is responsible for operating in compliance with all applicable procedures and policies. | 05/04/2025 |
| 1297 | Integra LifeSciences Plainsboro, NJ Microbiologist I Bachelor’s degree, in Microbiology or Biology Exp: 0-3 years |
The Microbiologist I will provide support to the QC Microbiology Laboratory as pertaining to the respective responsibilities. Performs functions such as executing laboratory testing for in-process and finished good products, water, stability studies, and validation studies as well as performs environmental monitoring. This position is responsible for operating in compliance with all applicable procedures and policies. | 05/04/2025 |
| 1298 | Integra LifeSciences Plainsboro, NJ Laboratory Technician II Bachelor’s or Masters Degree Exp: Bachelors: 1-3 years; Master's: 0-2 years |
Reporting to the Lab Operations Manager, Bldg. 104, this position is responsible for performing specialized duties required for the operations of the R&D lab, which includes supporting daily lab operations, assisting in driving lab compliance, supporting EHS compliance monitoring, document control and record management, inventory control, receiving, equipment maintenance, vendor management, technical project executions, and assisting in activities geared towards bio-/chemical safety and lab hygiene. | 05/04/2025 |
| 1299 | Integra LifeSciences Boston, MA Quality Engineer II - Design & Reliability Assurance Master’s degree in science, Engineering (Biomedical or Mechanical) or related discipline Exp: 0-2 years |
The Quality Design and Reliability Assurance (DRA) Engineer II is responsible for the efficient and compliant support of New Product Development (NPD) and Sustaining/Remediation project(s) of varying scope and complexity in the Tissue Technology (TT) division, specifically the Boston/ Braintree site. The role contributes and supports the design and development of new and improved products. The (DRA) Engineer II will interact with external design and development partners, participating on cross-functional project teams through all phases of the product development process, and assisting the technical team with planning, executing, documenting, and communicating testing activities. The role works with Product Development, Project Management, Regulatory, Marketing and Medical Affairs. | 05/04/2025 |
| 1300 | Integral Molecular Philadelphia, PA Lab Manager, MPA Bachelor's degree in Biology or related field Exp: 1-2 years |
Our close-knit, medium-sized company is composed of smart, curious, diverse scientists who take an active interest in the scientific and technical development of our team members. We are seeking a skilled and organized Laboratory Manager to oversee our cell and molecular biology research and production facility. This role focuses on operational oversight and team management to ensure efficient laboratory operations and support of scientific teams. | 05/04/2025 |
| 1301 | Integral Molecular Philadelphia, PA Research Associate Bachelor’s degree in biology, bioengineering, or a related field Exp: 1-2 years |
Our close-knit, medium-sized company is composed of smart, curious, diverse scientists who take an active interest in the scientific and technical development of our team members. We seek a Research Associate I to join our dedicated group of scientists. A desirable candidate will have the skills to culture mammalian and/or bacterial cells, perform DNA mini-preps, and complete bacterial transformations or cell transfections. | 05/04/2025 |
| 1302 | Integral Molecular Philadelphia, PA Research Technician Bachelor's degree in Biology, Chemistry, medical technology or related field Exp: 6 months |
Our company is in an exciting growth phase where we are launching new products and reaching new markets. To support our growth, we seek a Research Technician to join our Membrane Proteome Array research team. | 05/04/2025 |
| 1303 | Integrated DNA Technologies (IDT) Coralville, IA QA Complaint Analyst Bachelor's degree in Biological Sciences or related field (e.g., Biomedical Engineering, Systems Engineering, Pharmacology, Chemistry) Exp: 1-2 years |
This position is part of the Quality Assurance Department located in Coralville, IA and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things. In this role, you will have the opportunity to: Contribute to the continuous improvement of product safety +compliance by effectively managing and resolving quality complaints. Communicate with internal team members and external customers to facilitate complaint investigation process. Receive and document complaints from various sources, including customers, healthcare professionals, and internal stakeholders. Work closely with cross-functional teams, including Scientific Application Support (SAS), Quality Assurance, Regulatory Affairs, Product Development, and manufacturing to investigate and resolve complaints. Support quality system investigations, including issue reviews, nonconformances, CAPAs, SCARs, as needed. | 05/04/2025 |
| 1304 | Integrated DNA Technologies (IDT) Coralville, IA Process Development Engineer I Bachelor’s degree in STEM curriculum Exp: 1+ years |
This position is part of the Process Development Department located in Coralville, Iowa and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debates, and are inclusive. Together, we accomplish great things. | 05/04/2025 |
| 1305 | Interius BioTherapeutics Philadelphia, PA Lab Manager, MPA B.S. in Life Sciences Exp: 1-2 years |
As a detail-oriented and thorough Lab Manager, you will be joining a close-knit team that works in sync to ensure our labs are running smoothly. You will be an integral part of the team ensuring the safety of our lab personnel, the fidelity of our data, and the efficient day-to-day operations of our lab space. Bringing your uncanny ability to prioritize for maximum efficiency, your approachable nature, and your appetite to learn, you will be responsible and accountable for several activities from overseeing delivery logistics to tracking and ordering supplies. If knowing that you will never have a boring day in a fast-paced biotech company excites you, then being a part of the Lab Operations team at Interius will not disappoint. | 05/04/2025 |
| 1306 | Iovance Biotherapeutics Tampa, FL Research Associate II Master’s Degree in Cellular Biology, Molecular Biology, Immunology, or related discipline Exp: 0-2 years |
The Research Associate II will support research programs developing methods to optimize the anti-tumor activity of tumor-infiltrating lymphocytes (TILs) for therapeutic applications. A successful candidate will have experience with aseptic cell culture techniques and cell-based immunological assays. Prior experience with processing blood and solid tissue samples, as well as isolation and ex vivo manipulation of T cells and other relevant immune cells is beneficial. This role is a lab-based and will report to Iovance’s Tampa, FL facility. | 05/04/2025 |
| 1307 | Iovance Biotherapeutics Tampa, FL Process Development Associate Master’s in a life science or STEM-related discipline Exp: 0+ years |
The Process Development Associate I will support process development projects and technology transfer activities related to genetically and non-genetically engineered Tumor Infiltrating Lymphocyte (TIL) clinical trials. A successful candidate will have experience with aseptic cell culture techniques and cell-based immunological assays. Prior knowledge of cGMP practices is beneficial in this role. | 05/04/2025 |
| 1308 | Iovance Biotherapeutics Philadelphia, PA Quality Control Analyst I- Microbiology (Night Shift) Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Exp: 0-4 years |
The Quality Control Analyst I- Microbiology will support quality control testing operations at Iovance’s Cell Therapy Center (iCTC) and/or iPBMC manufacturing site (IOVA-A). The quality control testing programs include in-process and final drug product microbial testing such as bioburden, endotoxins, mycoplasma, gram stain, environmental monitoring, and sterility techniques. This position works across different shifts. Depending on your assigned shift, you may be required to work overtime, weekends, and holidays to complete assigned work. | 05/04/2025 |
| 1309 | Iovance Biotherapeutics Philadelphia, PA Quality Control Analyst I, Microbiology (Wed-Sat Day 7am – 6pm) Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Exp: 0-4 years |
The Quality Control Analyst I- Microbiology will support quality control testing operations at Iovance’s Cell Therapy Center (iCTC) and/or iPBMC manufacturing site (IOVA-A). The quality control testing programs include in-process and final drug product microbial testing such as bioburden, endotoxins, mycoplasma, gram stain, environmental monitoring, and sterility techniques. This position works across different shifts. Depending on your assigned shift, you may be required to work overtime, weekends, and holidays to complete assigned work. | 05/04/2025 |
| 1310 | Iovance Biotherapeutics Philadelphia, PA MSAT Specialist I B.S degree in a relevant discipline Exp: 1 year |
The MSAT Specialist I is a Manufacturing Operations cell therapy subject matter expert. The MSAT Specialist I reports to the Senior Manager, MSAT and EM and is responsible for manufacturing data analysis, contributing to deviation root cause analysis, and owning steps of the manufacturing process tech transfer. The MSAT Specialist is also responsible for protocol and report authoring, oversight of manufacturing operations, and execution of MSAT laboratory activities. | 05/04/2025 |
| 1311 | Iovance Biotherapeutics Philadelphia, PA Quality Control Compliance Specialist, CAPAs & Change Controls Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Exp: 1-3 years |
Iovance Biotherapeutics is a growing, late-stage company focused on the development and commercialization of novel cancer immunotherapies. Iovance is seeking a Quality Control (QC) Compliance Investigator who will in advance and close QC related investigations. Strong technical writing skills are required. Experience in a CAR-T or TIL environment is a plus. The ideal candidate will have experience working in a GMP-regulated laboratory with experience in writing investigations. | 05/04/2025 |
| 1312 | Iovance Biotherapeutics Philadelphia, PA Quality Control Specialist I, Compliance Investigator Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Exp: 1-3 years |
Iovance Biotherapeutics is a growing, late-stage company focused on the development and commercialization of novel cancer immunotherapies. Iovance is seeking a Quality Control (QC) Compliance Investigator who will in advance and close QC related investigations. Strong technical writing skills are required. Experience in a CAR-T or TIL environment is a plus. The ideal candidate will have experience working in a GMP-regulated laboratory with experience in writing investigations. | 05/04/2025 |
| 1313 | IQVIA Durham, NC Associate Scientist, Laboratory Operations Bachelor’s Degree in a chemical, physical, biological, or clinical laboratory science, medical laboratory technology, or cytotechnology Exp: 6 months |
We are seeking a Associate Scientistto join Q2 Solutions, IQVIA’s laboratory business at Durham, NC. The Associate Scientistwill perform routine analysis and laboratory testing procedures, ensuring compliance with SOPs and regulatory guidelines while supporting quality assurance and operational efficiency. | 05/04/2025 |
| 1314 | IQVIA Valencia, CA Associate Scientist Bachelor’s Degree in a chemical, physical, biological, or clinical laboratory science; medical laboratory technology; or cytotechnology Exp: 6 months |
We are seeking an Associate Scientist to join Q² Solutions, IQVIA’s laboratory business at Valencia, CA. Responsible for conducting routine analysis and laboratory testing procedures while ensuring compliance with SOPs, regulatory guidelines, and quality standards. This position involves data analysis, documentation, and collaboration within a fast-paced laboratory environment. | 05/04/2025 |
| 1315 | IQVIA Valencia, CA Clinical Data Assistant 2 Bachelor’s Degree in chemistry, biology, or medical laboratory technology Exp: 6 months |
The Clinical Data Assistant 2 is responsible for activities including data entry, primary and secondary quality control (QC), and release of RQCQ and EAF requisitions across accessioning platforms. Responsibilities also include managing RITM ticket requests, overseeing secondary passes for special studies, and ensuring team tasks are completed daily. Additional duties may involve the receipt, storage, and shipment of clinical specimens, routine troubleshooting, and guiding entry-level staff on basic department procedures. | 05/04/2025 |
| 1316 | IQVIA Durham, NC Immunoassay Associate Scientist Bachelor’s degree in chemistry or a related field. Exp: 1 year |
As an Immunoassay Associate Scientist, you will execute laboratory experiments with precision, contribute innovatively to scientific procedure design, and uphold the highest standards of Good Laboratory Practices (GLP) for our clients. You’ll not only set up and conduct experiments but also manage laboratory equipment, ensuring protocols are meticulously followed under the guidance of a dedicated lab services manager, researcher, or scientist. | 05/04/2025 |
| 1317 | Jnana Boston, MA Research Associate, Early Discovery Bachelor’s or Master’s degree in Biology, Biochemistry, or a related discipline Exp: 1-2 years |
Jnana Therapeutics is seeking an enthusiastic, highly motivated Research Associate to join our multidisciplinary team. This position offers the opportunity to contribute across Chemical Biology and Compound Management, supporting cutting-edge drug discovery efforts to unlock challenging targets using our novel hit generation platform and a variety of high-throughput, cell-based, and biochemical assays. This is an excellent opportunity for someone excited to grow their career in biotech, gaining exposure to both experimental science and core infrastructure that drives early discovery. | 05/04/2025 |
| 1318 | J-STAR Research Cranbury, NJ Research Scientist of Crystallization R&D MS or BS. in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related field Exp: 1-5 years |
We are seeking a highly motivated and skilled Research Scientist to join our Crystallization R&D Department at Porton J-STAR. In this role, this position is responsible for leading group or contributing individually to conduct Solid Form Studies and pre-formulation will search for the right solid form and develop formulations to support preclinical and Phase I studies including PK, PD, efficacy, tox studies. This role is also responsible for Crystallization Process Development will develop crystallization processes to define and control final solid form of drug substances with desired solid-state attributes needed for optimum performance as well as drug intermediates for robust purification. The responsibilities of the position include, but are not necessarily limited to, the items listed below. | 05/04/2025 |
| 1319 | Jubilant HollisterStier Spokane, WA Technologist I, Engineering Bachelor’s degree in Engineering, Drafting, or related Scientific or Technical field Exp: 1-5 years |
Holds a general responsibility for projects associated with facilities or production equipment throughout the manufacturing facility. Performs tooling design, maintains engineering drawing system, and tracks production equipment performance to implement efficiency and uptime improvements. Responsibilities may include equipment installation, electrical or mechanical work, equipment optimization, equipment spare parts setup and warehousing, and troubleshooting of equipment. Supports construction activities for various capital improvement projects as required. | 05/04/2025 |
| 1320 | Jubilant HollisterStier Spokane, WA Scientist II, QC (Weekday Day) Bachelor’s Degree in Chemistry, Biology, or related hard science Exp: 1 year |
The QC Scientist II performs the analysis on allergenic and client components, raw materials, intermediates, and finished products following written procedures, providing the data required to determine raw material/product disposition. | 05/04/2025 |
| 1321 | Jubilant HollisterStier Spokane, WA Process Engineer I/II/III/Sr. Bachelor’s of Arts or Science with a major in Biology, Chemistry, Physics, or Engineering Exp: 0-5 years |
The Process Engineer I/II/III/Sr. provides ownership and focus for pharmaceutical processes and technical transfers at Jubilant HollisterStier. This position will engage in and manage projects and multi-disciplinary teams with direct supervision. The process engineer will also contribute technical direction for complex projects and exhibit clear communication skills with all levels of employees. | 05/04/2025 |
| 1322 | Jubilant HollisterStier Spokane, WA QC Scientist I-IV (Weekend Nights) Bachelor of Science in Chemistry, Biology, or related hard science Exp: No Exp |
The QC Scientist I/II/III/IV performs the analysis on allergenic and client components, raw materials, intermediates, and finished products following written procedures, providing the data required to determine raw material, product disposition. In addition, this position demonstrates leadership, teamwork and technical expertise. | 05/04/2025 |
| 1323 | Jubilant HollisterStier Spokane, WA Microbiologist I/II Bachelor of Science in Microbiology or related hard science with microbiology Exp: No Exp |
The QC Microbiologist I-II performs the microbial analysis on allergenic and client components, raw materials, intermediates, and finished products following written procedures, providing the data required to determine raw materials/product disposition. | 05/04/2025 |
| 1324 | Juvena Therapeutics Redwood City, CA Vivarium Research Technician BA Exp: 1-3+ years |
Juvena Therapeutics is seeking a highly motivated Vivarium Research Technician to join our dynamic research team in Redwood City, CA. This role will contribute to the growth of our research portfolio by supporting vivarium operations to advance the development of novel rejuvenating therapies. This position is ideal for a talented, highly motivated and results driven individual who will thrive in a fast-paced, innovative, start-up environment. The individual will report to Senior Scientist/Director in vivo Pharmacology. | 05/04/2025 |
| 1325 | FUJIFILM Diosynth Biotechnologies College Station, TX Quality Assurance-Compliance Specialist II Master’s degree in a related science concentration Exp: 1 year |
The Quality Assurance - Compliance Specialist II - Audit and Inspection will support all associated responsibilities in compliance with FUJIFILM Diosynth Biotechnologies quality policies and site SOPs to ensure regulatory compliance. | 04/15/2025 |
| 1326 | FUJIFILM Diosynth Biotechnologies College Station, TX QA Analyst III Master’s Degree in Biology or Chemistry Exp: 1+ years |
The Quality Assurance (QA) Analyst III, under minimal direction, will be responsible for review and/or approval of basic and technical documentation, drafting and reviewing of internal Quality policies and procedures, performing product related activities, performing Quality audit functions, performing product release activities, identifying process and Quality System improvements, and acting as a QA liaison internally and externally. | 04/15/2025 |
| 1327 | FUJIFILM Diosynth Biotechnologies Research Triangle Park, NC Production Technician II BS/BA Exp: 1+ years |
Fujifilm Diosynth Biotechnologies U.S.A., Inc. is seeking a Production Technician II. The successful candidate will be performing glass wash, cell culture sterilization techniques, support mammalian cell culture manufacturing processes, sustaining purification of bio-pharmaceuticals, operate various process equipment, documenting daily manufacturing operations in a cGMP environment, working with single- use and stainless steel bioreactors, fermentation, and/or filtration. | 04/15/2025 |
| 1328 | FUJIFILM Diosynth Biotechnologies College Station, TX Manufacturing Process Engineer I Bachelor’s degree in Science, Engineering, or other related field Exp: 1 year |
The Manufacturing Process Engineer I is an integral part of the Manufacturing Technical Operations department located in College Station, Texas. This position will report directly to the Manager of Technical Operations, Manufacturing. | 04/15/2025 |
| 1329 | FUJIFILM Diosynth Biotechnologies Holly Springs, NC Engineer 2, Upstream - MSAT Master’s degree in Engineering, Life Science or Chemical Engineering Exp: No exp |
The Upstream Engineer/Scientist 2 will provide tech transfer support and technical oversight for a large-scale cell culture in monoclonal antibody manufacturing. | 04/15/2025 |
| 1330 | FUJIFILM Diosynth Biotechnologies College Station, TX QA Analyst II Master’s degree in a related science concentration Exp: 1+ years |
The Quality Assurance (QA) Analyst II, under general direction, will be responsible for review and/or approval of basic and technical documentation; Drafting and reviewing of internal Quality policies and procedures; Assisting in and performing product related activities; Assisting in and performing Quality audit functions; Identifying process and Quality System improvements; Acting as a QA liaison internally. | 04/15/2025 |
| 1331 | FUJIFILM Diosynth Biotechnologies College Station, TX Quality Control - Stability Coordinator I Bachelor’s degree in Science, Engineering, or other related field Exp: 1 year |
The QC Stability Coordinator I, will construct, maintain, and oversee the Quality Control Testing of Stability programs to include developing a schedule of pull dates, overseeing testing of each pull, and generating summaries from the data. The Quality Control Coordinator I, under general direction, will be responsible for implementing a Quality Control Stability Program that will encompass the needs of the client for each program. The position will require frequent communication with the Chemistry, Cell Biology, Microbiology, and Quality Assurance groups to coordinate execution of testing, deviation management, and issuance of deliverables. The Coordinator will have visibility to method qualification to ensure timing of stability laydowns. Close attention to detail is required to oversee scheduling the stability testing and compiling data, to facilitate meeting deadlines and milestones. Other responsibilities may include but are not limited to: ownership of CAPA’s and deviations, client meetings, attending planning meetings, communication of changes, and utilizing new software. | 04/15/2025 |
| 1332 | Fulgent Therapeutics Needham, MA Imaging Specialist I Bachelor’s Degree in the Sciences Exp: 1-3 years |
The Imaging Specialist is responsible for performing Quality Control functions on all cases and taking digital microphotographs on designated cases for final pathology report. The Imaging Specialist will follow the direction of the supervisor while taking initiative in performing and promoting quality and efficiency within the department. The Imaging Specialist will be trained in the expected task in order to meet the competency set by the department. | 04/15/2025 |
| 1333 | Garuda Therapeutics Watertow, MA Manufacturing Associate BA/BS degree Exp: 1 year |
Garuda Therapeutics is seeking a motivated Manufacturing Associate or Senior Manufacturing Associate to support routine GMP Manufacturing operations. This includes day-to-day operational tasks including but not limited to Cell Culture in a clean room environment, GMP Materials Logistics, and Environmental Monitoring within Garuda’s GMP manufacturing space. This is an on-site role, primarily in Watertown, MA with occasional work in Cambridge MA. Some travel between sites is required. | 04/15/2025 |
| 1334 | Genezen Indianapolis, IN Analytical Development Laboratory Technician B.S. degree in Biology, Biochemistry, Molecular Biology, or similar field Exp: 1+ years |
We are looking for someone with high emotional intelligence and is comfortable working closely across the team to join us in facilitating the production of viral vectors. The Laboratory Associate I/II will be needed to perform analytical assays for viral vector process development, assist with method development, document experiments, help with lab maintenance and execute assay qualifications. This position calls for an independent thinker who can work seamlessly in a matrixed environment. | 04/15/2025 |
| 1335 | Genezen Indianapolis, IN Manufacturing Technician I/II/III BS degree in Biology, Biochemistry, Molecular Biology, or similar field Exp: 1-5 years |
Responsible for supporting projects from advanced laboratory techniques related to viral vector production and analytics to routine performance of upstream and downstream manufacturing operations including aseptic cell culture technique, preparing solutions and media, molecular biology techniques, chromatography, TFF and general cleanroom sanitization/area maintenance. The position requires working independently, but also under the supervision of experienced personnel. | 04/15/2025 |
| 1336 | Genezen Lexington, MA QC Analyst - Microbiology (Contract) BA or BS in Microbiology or other related science Exp: 0-3 years |
The QC Analyst will be responsible for routine and non-routine QC sampling and testing for the quality of products manufactured for our clients. QC is responsible for execution of the Environmental Monitoring (EM) program in place to monitor Genezen's controlled manufacturing environments (cleanrooms) as well as monitoring of utility systems including Water for Injection (WFI), Pure Steam, Purified Water, Compressed Air and Gas systems. These activities are all performed in accordance with cGMP guidelines and are supported by departmental and interdepartmental policies and standard operating procedures (SOPs). This position is based at Genezen’s state-of-the-art facility in Lexington, MA. This role supports daily operations as well as occasional weekend and holiday operations. This may include but is not limited to in-process monitoring and testing, lot release testing, and stability testing. Supporting activities for quality systems: utility monitoring excursions, non-conformance, deviations, corrective and preventive actions (CAPAs), investigations, Out of Specifications (OOS), and change controls may be required. | 04/15/2025 |
| 1337 | GenScript Pennington, NJ QC Scientist - Microbiology Master’s degree in Microbiology, Molecular Biology, Biochemistry, or related scientific field Exp: 1 year |
The position reports to the Director of QC, is ideally suited for a professional with extensive technical knowledge, and a proven track record of developing and carrying out processes, that are suitable for use in GMP manufacturing of a wide range of clinical trial materials, and participating in the technology transfer. There is a great opportunity to lead and evolve this function within a CDMO business, to support a broad portfolio and advance the manufacturing capabilities to deliver products to the client projects that transform the lives of patients. | 04/15/2025 |
| 1338 | GenScript Pennington, NJ Specialist, Bioprocess -Upstream Process Bachelor’s degree in science or engineering Exp: 0-5 years |
The position will work within the Upstream Processing group and performs the following activities while executing upstream operations: Preparation of stock solutions, buffers and media. Filtration of stock solutions, buffers and media. Set-up and operate disposable fermenters / bioreactors and other disposable bioprocess equipment including depth filtration. Passage and expansion of microbial and mammalian cell lines. The position also supports relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate. | 04/15/2025 |
| 1339 | GenScript Redmond, WA EHS Specialist Bachelor’s degree in Engineering or Science Exp: 0-3 years |
We are seeking a Part-Time EHS Specialist. This role reports to the Director of EHS Department and is ideally suited for an individual with an understanding of health, safety and environmental equipment, regulations, and practices. The selected candidate will assist other EHS team members, support the Quality Assurance Function, and assist Facilities Services team with EHS equipment and non-EHS laboratory equipment, operations, and compliance issues. Excellent opportunity for additional learning and development. | 04/15/2025 |
| 1340 | Getinge Wayne, NJ Engineer I, Production Bachelor of Science degree, preferably in Biomedical, Mechanical, Manufacturing Engineering or equivalent Exp: 0-2 years |
The primary responsibility for this Engineer I, Production Engineering position will be reviewing production documentation and addressing deficiencies found, performing equipment qualifications, and other improvements related to compliance issues. Lead and execute process validation requirements in parallel with identifying and implementing improvement and cost elimination projects for manufacturing. This position will report to the Supervisor, Manufacturing Engineering. | 04/15/2025 |
| 1341 | Getinge Englewood, CO Laboratory Technician II, Microbiology BS in microbiology or a related technical discipline Exp: 1-3 years |
Reporting to the Sr. Microbiologist, this position participates in activities related to applied biological research for ongoing analytical studies. Under the guidance of the Sr Microbiologist performs data analysis and communicates findings to the organization. In concert with other disciplines and peers, participates in, and guides the development of, protocols for biological research studies and evaluates alternate methodologies. Recommends materials, supplies, and equipment as required for studies. Develops and participates in the development and validation of both in process and finished product quality test methods. Under the guidance of the Sr. Microbiologist, perform tasks associated with a spore manufacturing process. Perform testing to support process improvement studies, process validation studies, design verification and design validation studies. | 04/15/2025 |
| 1342 | Globus Medical Audubon, PA Electrical Engineer MS in electrical engineering Exp: 1+ years |
We are seeking a highly skilled and motivated Electrical Engineer to join our rapidly growing Digital Health team. You will work closely with a dynamic team of electrical, software, and mechanical engineers to conceptualize and commercialize innovative medical devices to meaningfully impact the lives of patients with musculoskeletal disorders. The ideal candidate will have a strong background designing, building, and testing embedded electrical systems, including firmware design and development. This role requires a balance of creative thinking, analytical design, hands-on prototyping and testing, and systematic product development. | 04/15/2025 |
| 1343 | Globus Medical Methuen, MA Associate Project Engineer, Electrical Bachelor’s degree in electrical engineering Exp: 1-3 years |
Our rapidly growing medical robotics division is searching for enthusiastic electrical engineers wanting to make a difference. Our skillful engineers develop medical robots by working with top surgeons and cross-functional engineering teams. The Electrical Engineer will be part of the electrical team responsible for designing and implementing electronic circuits and electro-mechanical sub-systems for surgical robotic products. The position will be a hands-on one with the individual capable of creative and systematic product development with minimum supervision. | 04/15/2025 |
| 1344 | Grand River Aseptic Manufacturing Grand Rapids, MI QC Microbiology Technician (Weekend Day Shift) Bachelor’s degree in Microbiology or a related field. Exp: 0-2 years |
The QC Microbiology Technician supports quality control and assurance by assisting the microbiology department with environmental monitoring, water testing, and client specific testing. This position will work Fri-Sun, 6pm-6am. | 04/15/2025 |
| 1345 | Grifols Clayton, NC Validation Engineer I Bachelors Degree in Engineering Exp: 0-2 years |
The Engineer I - Validation / Engineer II – Validation / Validation Specialist I position supports Fractionation, Purification, Filling, Utilities and/or capital projects as required. This position is responsible for assigned qualification and validation related activities related to supporting the Clayton NC site. | 04/15/2025 |
| 1346 | Grifols Clayton, NC Assistant Biologist BS degree in biology, chemistry, or related field Exp: 6-12 months |
This position is responsible for performing environmental monitoring of fill lines in SFF and PFF and also environmental monitoring of all classified production areas, including sampling of site utility systems. Environmental Assurance department must maintain adequate staffing to support all filling operations 24 hours per day, 7 days a week. In addition to routine environmental monitoring of the aseptic fill lines, this position is also responsible for executing the Quality Oversight program for the fill lines and also provides quality control approval of air flow visualizations conducted on site. This position is part of the budgeted staff necessary to complete this sampling and testing and to ensure that Clayton site environmental monitoring of the aseptic fill lines and other production areas and utility systems remain in a state of control. Must be able to perform tasks by following SOP’s and oral instructions. Must have precise, legible, and organized documentation skills. Candidates must also be willing to perform ones share of cleaning duties and housekeeping. | 04/15/2025 |
| 1347 | Grifols San Francisco, CA Research Associate Bachelor’s degree in Life Sciences or related discipline Exp: 1 year |
GigaGen, a subsidiary of Grifols, seeks a talented, highly motivated Research Associate to support the process development of our diverse antibody therapeutics pipeline. This will include cell line development, cell culture optimization, and bioreactor production, as well as purification and analytical characterization of antibodies and antibody derivatives. This position will offer exposure to drug development, from early research through development/manufacturing, with ample opportunity to learn new methods, design experiments, and present your work. | 04/15/2025 |
| 1348 | Grifols Clayton, NC Associate Stability Research Scientist II BS Degree Exp: 1-2 years |
The incumbent will work in a supporting function to provide scientific and technical assistance in the research and development of plasma derived or recombinant proteins. The position provides support to the Stability Group by overseeing all facets of the stability program that are related to oversight of the stability chamber areas, storage, delivery and documentation of the sample inventory in order to maintain a compliant stability program for licensed products and developmental projects, ensuring on-going safety and quality of our products. | 04/15/2025 |
| 1349 | Grifols Vista, CA Manufacturing Technician 1 Bachelor’s degree Exp: 1-2 years |
The Manufacturing Technician I performs fundamental tasks within a GMP environment in support of more complex manufacturing operations. The Tasks include, but are not limited to, cleaning and maintaining the work place so that it meets the standards for controlling bioburden levels; cleaning operating equipment per applicable procedures so that it meets the standards established to prevent product contamination and maintaining records/logs neatly and accurately and in accordance with current standard procedures. The technician performs job tasks in a safe manner while following specific department safety rules. | 04/15/2025 |
| 1350 | Grifols San Diego, CA QC Support Analyst 3 - Blood Typing Solutions B.A. or B.S. in a biological science or chemistry Exp: 0-2 years |
Grifols Diagnostic Solutions Inc is seeking a Quality Control Support Analyst 3 to join our Immunohematology Quality Control department for Reagent Red Blood Cells (RRBC) and Gel Cards in San Diego, CA. This position will be reporting to the QC Supervisor. The primary job function of the QC Support Analyst 3 is to test and release raw materials, sub-assemblies or finished goods. In order to be successful in this role, candidates must have a bachelor’s degree in Biological Sciences or Chemistry with 0 to 2 years of relatable QC experience. Experience working and handling blood products, preferred. | 04/15/2025 |
| 1351 | Grifols Clayton, NC Engineer - Global Process Engineering Bachelor's Degree in Engineering or related field. Exp: 0-2 years |
The Process Engineer demonstrates consistent application of technical knowledge and/or regulatory knowledge in the Process Engineering discipline. Develops and implements solutions. Leads projects of larger scope (or portions of projects) and is often called upon by peers for guidance. Directs project or discipline teams. Meets customer needs in support of business goals. | 04/15/2025 |
| 1352 | Guardant Health Redwood City, CA Biospecimen Associate I (Thursday- Saturday) Bachelor of Arts or Science in Biomedical Laboratory Science, Clinical Science or related field Exp: 1-2 years |
The Biospecimen Associate I supports the management of patient samples and provides the link between the Clinical Operations and Client Services teams. The Biospecimen Associate I is responsible for receiving, unpacking, processing, and recording samples sent for laboratory testing under the supervision of the Biospecimen Management Supervisor. The Biospecimen Associate I has demonstrated an understanding of laboratory workflow. | 04/15/2025 |
| 1353 | Guardant Health Redwood City, CA Clinical Laboratory Associate II (Tuesday-Saturday) Bachelor’s degree or equivalent in Biomedical Laboratory Science, Clinical Science or related field Exp: 1 year |
The Clinical Laboratory Associate (CLA) II is responsible for supporting the daily operations of the Clinical Laboratory and assisting the Clinical Laboratory Scientist (CLS) during patient testing. In addition to the primary role of CLA, there will be a need to provide back-up support to the other groups (Reporting, Biospecimen Management, QC, etc.). The CLA II may serve as a lead to the CLA team to coordinate tasks, divide workload, manage equipment usage schedule and documents reviewing/filing process as assigned. The CLA II has demonstrated the skills and competency to assist the CLSs in automated sample processing and in all other support functions. | 04/15/2025 |
| 1354 | Guardant Health Redwood City, CA Biospecimen Associate I (Monday-Friday) Bachelor of Arts or Science in Biomedical Laboratory Science, Clinical Science or related field Exp: 1-2 years |
The Biospecimen Associate I supports the management of patient samples and provides the link between the Clinical Operations and Client Services teams. The Biospecimen Associate I is responsible for receiving, unpacking, processing, and recording samples sent for laboratory testing under the supervision of the Biospecimen Management Supervisor. The Biospecimen Associate I has demonstrated an understanding of laboratory workflow. | 04/15/2025 |
| 1355 | Guardant Health Redwood City, CA Clinical Laboratory Associate II (Sunday-Tuesday) Bachelor’s degree or equivalent in Biomedical Laboratory Science, Clinical Science or related field Exp: 1 year |
The Clinical Laboratory Associate II (CLA II) is responsible for supporting the daily operations of the Clinical Laboratory and assisting the Clinical Laboratory Scientist (CLS) during patient testing. In addition to the primary role of CLA, there will be a need to provide back-up support to the other groups (Reporting, Biospecimen Management, QC, etc.). The CLA II may serve as a lead to the CLA team to coordinate tasks, divide workload, manage equipment usage schedule and documents reviewing/filing process as assigned. The CLA II has demonstrated the skills and competency to assist the CLSs in automated sample processing and in all other support functions. | 04/15/2025 |
| 1356 | Guardant Health Redwood City, CA Clinical Laboratory Associate II (Wednesday-Saturday) Bachelor’s degree or equivalent in Biomedical Laboratory Science, Clinical Science or related field Exp: 1 year |
The Clinical Laboratory Associate II (CLA II) is responsible for supporting the daily operations of the Clinical Laboratory and assisting the Clinical Laboratory Scientist (CLS) during patient testing. In addition to the primary role of CLA, there will be a need to provide back-up support to the other groups (Reporting, Biospecimen Management, QC, etc.). The CLA II may serve as a lead to the CLA team to coordinate tasks, divide workload, manage equipment usage schedule and documents reviewing/filing process as assigned. The CLA II has demonstrated the skills and competency to assist the CLSs in automated sample processing and in all other support functions. | 04/15/2025 |
| 1357 | HemoSonics Durham, NC R&D Engineer Master’s degree in Engineering or related discipline Exp: 0 years |
Being able to wake up in the morning knowing that your work makes a difference in the lives of others - that's the best kind of motivation. If you're looking for a company where you can combine a passion for improving patient care and outcomes with the skills and experience you've spent a career developing, then HemoSonics may just be your perfect fit! This role is on-site in Durham, North Carolina - working remotely from other parts of the country is not an option for this role, so all candidates must be local or planning to move for this position. | 04/15/2025 |
| 1358 | Hesperos Orlando, FL Engineer Associate I/II Bachelor’s degree of Engineering Exp: 1 year |
You are experienced in software development for scientific data and scientific equipment, and developing algorithms, software, and interfaces. You are conscientious and pay almost obsessive attention to detail, as organized documentation is second nature. You are curious, love learning, and are eager to take on hard problems. You thrive in a fast-paced environment and enjoy pushing the edge of what is possible. You are resourceful and like to work independently but are not shy to ask for advice. You are a cross-disciplinary team member, who is excited to work with and learn from other engineers, biologists, chemists, modelers, and experimentalists. You are comfortable communicating across teams. You deliver. You know that what matters is delivering a solution that works every time. | 04/15/2025 |
| 1359 | HighRes Beverly, MA Associate Manufacturing Engineer Bachelor's degree in Mechanical or Manufacturing Engineering Exp: 0-2 years |
The Associate Manufacturing Engineer will primarily be focused on creating and implementing process improvements and strategies to optimize manufacturing efficiency. This includes sustaining, continuous improvement, and new product introduction efforts to scale with the dynamic workload. They will also be working together with the technician workforce to provide production floor support, as well as being a cross-functional resource to liaison between operations and other engineering teams to ensure communication and compliance across all facets of manufacturing. | 04/15/2025 |
| 1360 | HighRes Remote, CA Jr. Field Service Engineer Bachelor’s degree in electromechanical/life science/engineering Exp: 0-3 years |
The Field Service Engineer position at HighRes Biosolutions is the primary role responsible for installation, maintenance, troubleshooting and repair of systems and devices at customer sites. This position specializes in the hardware aspect of the products, coordinating with the Automation Support Engineer role in Customer Support and collaborating with the manufacturing and commissioning department (software and configuration-focused) for full coverage support of the products. Levels I and Junior are roles for carrying out Field Service Engineer responsibilities in either learning or assisted modes, with oversight and assistance from a team lead, supervisor, manager, or skilled technical Customer Service colleague(s). | 04/15/2025 |
| 1361 | Hikma Cherry Hill, NJ Quality Lab Associate I, Micro BS/BA Degree in Microbiology or Biology Exp: 0-2 years |
Perform functions within the Microbiology Laboratory and/or conduct critical microbiological analysis on test articles from all stages of the manufacturing process from incoming raw materials to finished goods. The duties also include equipment maintenance and LIMS management. | 04/15/2025 |
| 1362 | Hikma Cherry Hill, NJ Manufacturing Specialist - 2nd Shift B.S. in technical discipline Exp: 0-3 years |
The Manufacturing Specialist will assist the shift lead in a hands-on approach to overseeing production activities including, filling, sterilization, component and equipment prep, and compounding. Completes quality systems activities including commitments, deviations, DCEs, and SOP revisions as necessary. Responsible for meeting budget, quality, and production goals, setting standards, and making employment and staffing recommendations. Interprets manufacturing policies, procedures, and programs | 04/15/2025 |
| 1363 | Hikma Cherry Hill, NJ QA Inspector Bachelor’s Degree in Science or equivalent Exp: 0-2 years |
The QA Inspector monitors in-process product quality for Filling and Inspection and Packaging of parenteral products. The QA Inspector performs visual and functional testing of products against statistically based sampling plans. In addition, the QA Inspector performs routine inspection and testing of components following Standard Procedures and specifications as required by production schedules. In performing the above duties, the individual is responsible for accurately and clearly documenting test results following cGMPs. This position participates in rotation for weekend coverage and as needed during the work week. | 04/15/2025 |
| 1364 | ICU Medical Southington, CT Engineer I, Quality Bachelor’s degree in Engineering or STEM Exp: 0-2 years |
Engineer I, Quality will support the ICU Quality Operations Department and report to the Quality Operations Manager. They are responsible for sustaining manufacturing and validations through adherence to established design control processes, good quality and documentation practices. The key responsibility of this position is to exercise judgement and act while adhering to defined quality procedures during project support & improvement. Engineer I, Quality will complete basic projects assigned by more experienced engineers and managers. They work on projects/matters of limited complexity in a support role while being closely managed. | 04/15/2025 |
| 1365 | Emerald Cloud LAb Austin, TX Laboratory Operations Shift Manager Bachelors or master’s degree in industrial engineering Exp: 1-4 years |
As a Shift Manager, you will be responsible for managing a shift of approximately 15-20 individuals. As the leader of this team, you will be responsible for setting high standards for your shift while ensuring all performance metrics are met on time and within cost. In this role you’ll act as a key business partner to operations leadership and cross-functional partners, assisting with driving efficiency and implementing scalable processes. This position requires a results-oriented, high-energy individual with the stamina and mental agility to thrive in a fast-paced startup environment. | 04/07/2025 |
| 1366 | Emerald Cloud LAb Austin, TX Laboratory Operator I, II, & III Bachelor’s degree Exp: 1-3 years |
The demand for our service is growing, and to meet that demand, we are recruiting Lab Operators looking to explore opportunities in the biotech space and grow with our organization. Qualified candidates will receive comprehensive lab and safety training, allowing them the ability to run protocols in our Austin facility. These protocols are critical to sustaining the high-quality operations of the facility and provide experience working in ECL’s unique, process-driven lab environment with our integrated software tools. | 04/07/2025 |
| 1367 | Empirico Madison, WI Assistant Scientist - Drug Discovery Bachelor’s degree in Molecular Biology, Biochemistry or a related discipline Exp: 1 year |
Empirico, a clinical-stage biotechnology company that combines unmatched expertise in human genetics-driven target discovery with world-class capabilities in siRNA medicines, is looking for a talented scientist to help advance our growing pipeline. This position offers a unique opportunity to participate in and support multiple projects in diverse therapeutic areas, across different stages of preclinical development. You will work closely with other scientists that have a passion for finding novel approaches toward the treatment and prevention of disease. | 04/07/2025 |
| 1368 | Empirico Madison, WI Assistant Scientist / Associate Scientist - CMC Bachelor’s degree in Chemistry or Chemical Engineering with an understanding of organic and analytical chemistry Exp: 1-3 years |
Empirico, a clinical-stage biotechnology company that combines unmatched expertise in human genetics-driven target discovery with world-class capabilities in siRNA medicines, is looking for a chemist with an interest in solid-phase oligonucleotide synthesis and analytics. This is an excellent opportunity for a highly motivated, creative scientist to be a vital member of our team. | 04/07/2025 |
| 1369 | Empirico Madison, WI Scientist / Senior Scientist - Oligonucleotide Chemistry Master’s degree in Organic Chemistry Exp: 1-7 years |
Empirico, a clinical-stage biotechnology company that combines unmatched expertise in human genetics-driven target discovery with world-class capabilities in siRNA medicines, is looking for a talented chemist with experience in solid-phase oligonucleotide synthesis and analytics. This is an excellent opportunity for a highly motivated, creative scientist to be a vital member of our team. | 04/07/2025 |
| 1370 | Endo Rochester, MI Chemist II, Quality Control Laboratory Master’s Degree in chemistry, chemical engineering or related field Exp: 1+ years |
The Chemist II, under general supervision, performs QC laboratory chemical analyses of raw materials, in-process materials, stability & finished products, and testing to support process validation. Detects, participates and reports on OOS/OOT/NOE and other investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. May train less senior staff. | 04/07/2025 |
| 1371 | Endo Rochester, MI Microbiologist I Master of Science degree in microbiology, biology or related field Exp: 1+ years |
Performs Quality laboratory microbiological analyses of materials including water testing, finished product testing, raw material testing, and method validation. Supports laboratory investigations of moderate scope and complexity while abiding by GMPs and GLPs. Has working knowledge of, and stays current with, regulatory guidance and compendia relevant to laboratories and pharmaceutical manufacturing. | 04/07/2025 |
| 1372 | Endo Rochester, MI Operations Engineer, Sterile Fill (afternoon) Bachelor’s Degree or higher in Engineering or Science related equivalent Exp: 1-3 years |
The Operations Engineer, Sterile Filling, works in a hands-on capacity in a fast-paced, cGMP environment and production support areas to process sterile and aseptic products. The specialist works in collaboration with Operations, Maintenance, Engineering, Supply Chain, Quality Assurance, and Pharmaceutical Technology and Validation for successful repeatable day-to-day manufacturing operations in the Sterile Filling Area. Position is responsible for working with operations team to mitigate gaps within the sterile filling operations. Position also facilitates maintaining departmental documentation and processing of batch documentation. Position is also trained to perform verification of process steps in support of departmental supervision. Knowledge of cGMP’s is essential to successful performance of the position. In partnership with the site leaders sponsors a quality and compliance focused site culture which embraces RFT (right first time) and CI (continuous improvement) expectations. | 04/07/2025 |
| 1373 | Endo Horsham, PA QC Analyst I - Microbiology B.S. in a Biological Science or related field Exp: 0-3 years |
The QC Analyst I – Microbiology will perform microbiological testing, release of in-process, intermediates and finished products, and testing for validation purposes. This role completes appropriate documentation to support testing procedures including data capture forms, equipment logbooks, and inventory forms. Additionally, this role is responsible for assisting with the writing of standard operating procedures (SOPs) and revision of existing documentation. | 04/07/2025 |
| 1374 | Endo Rochester, MI Quality Associate Specialist, Product Release BA/BS degree in a related discipline Exp: 0-1 year |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. All incumbents are responsible for following applicable Division & Company policies and procedures. | 04/07/2025 |
| 1375 | Endo Rochester, MI Operations Engineer, Sterile Filling (Days) Bachelor’s Degree or higher in Engineering or Science related equivalent Exp: 1-3 years |
The Operations Engineer, Sterile Filling, works in a hands-on capacity in a fast-paced, cGMP environment and production support areas to process sterile and aseptic products. The specialist works in collaboration with Operations, Maintenance, Engineering, Supply Chain, Quality Assurance, and Pharmaceutical Technology and Validation for successful repeatable day-to-day manufacturing operations in the Sterile Filling Area. Position is responsible for working with operations team to mitigate gaps within the sterile filling operations. Position also facilitates maintaining departmental documentation and processing of batch documentation. Position is also trained to perform verification of process steps in support of departmental supervision. Knowledge of cGMP’s is essential to successful performance of the position. In partnership with the site leaders sponsors a quality and compliance focused site culture which embraces RFT (right first time) and CI (continuous improvement) expectations. | 04/07/2025 |
| 1376 | Enovis Carlsbad, CA Test Engineer Bachelor’s degree in engineering (Mechanical or Biomedical) Exp: 1+ years |
Test Engineer is responsible for designing, developing, and testing mechanical systems and components. The engineer is responsible for producing and implementing designs and test procedures analyzing and troubleshooting mechanical systems and components and developing and testing prototypes. The engineer will participate in daily technical meetings to review project progression, performance of team members and recourse management. This position will serve as great transition from education to junior level for a young professional to further engineering skills in an array of projects. | 04/07/2025 |
| 1377 | Eurofins West Point, PA Lab Coordinator BS degree in Biology, Chemistry, Engineering, or related sciences Exp: 0+ years |
Performs routine checks on equipment to verify parts are in good condition, ensures equipment is functioning properly, and documentation and recordkeeping is maintained, Arranges equipment replacement and repairs as needed, Coordinates with laboratory staff, and safety to properly maintain and remain compliant in common/shared equipment including preventive maintenance (PMs), service, repair, calibration, and certification, Ordering new equipment, Prepares purchase requests, obtains quotes and interacts with purchasing personnel, Schedules and coordinates instrument installation, Facilitates instrument/equipment training with lab staff, Supporting Lab staff with lab maintenance, Freezer/ fridge maintenance, Benchling Inventory compliance, Shared reagent/ biologics inventory, Maintain/ order supplies in compliance with ‘hazardous materials’ (COSMIC), Submitting shipment requests- within and outside of the facility | 04/07/2025 |
| 1378 | Eurofins Indianapolis, IN Analytical Biochemist Bachelor's degree in biology, biochemistry, chemistry, or other related degree concentration Exp: 1-2 years |
Perform biochemical testing on samples including, but not limited to HPLC, CE, and physical properties, Use ALCOA to document test results in electronic notebooks. | 04/07/2025 |
| 1379 | Eurofins Portage, MI Scientist Bachelor's degree in biology, chemistry, or other related degree concentration Exp: 1-2 years |
Performing physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products (tablets, capsules, parenterals, devices, liquids, creams, and gels) and animal health product, Preparing standards and samples for analysis; running the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, HPLC, and dissolution apparatus, Executing method transfer protocols, Performing monthly maintenance of laboratory equipment, Working efficiently, documenting work clearly, and performing tests accurately, Ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations, Reads and understands analytical procedures (compendial and client supplied) and internal SOPs, Processes data, generates reports, and evaluates data, Trains others in laboratory procedures, Performs laboratory maintenance, Communicates with vendors and repair personnel, Writes investigations, Leads project/test areas and perform method transfers/feasibility studies, Preparing standards and samples for analysis; running the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, HPLC, and dissolution apparatus | 04/07/2025 |
| 1380 | Eurofins Lexington, MA Bioassay Scientist MS in Cell and Molecular Biology, Biochemistry, or Pharmaceutical concentration Exp: 6 months |
We are seeking a scientist with strong organizational skills, excellent oral and written communication, and keen attention to detail. The ideal candidate will support the development, optimization, and qualification of analytical methods in a compliance-based environment. This role involves method development, process support, documentation, and potential technology transfer, along with some analytical testing. The ability to work independently and collaboratively, along with self-motivation, adaptability, and a positive attitude, is essential. | 04/07/2025 |
| 1381 | Eurofins Frederick, MD Sample Management Technician, 2nd Shift BS degree in a science-related field Exp: 1-2 years |
We seek a highly motivated and detail-oriented Laboratory Technician to join our team. The successful candidate will possess a fundamental understanding of current Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs), ensuring compliance with industry standards on a daily basis. The role requires proficiency in laboratory operations, sample management, and collaboration across departments. | 04/07/2025 |
| 1382 | Eurofins Frederick, MD Sample Management Technician, 1st Shift BS degree in a science-related field Exp: 1-2 years |
We seek a highly motivated and detail-oriented Sample Management Technician to join our team. The successful candidate will possess a fundamental understanding of current Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs), ensuring compliance with industry standards on a daily basis. The role requires proficiency in laboratory operations, sample management, and collaboration across departments. | 04/07/2025 |
| 1383 | Eurofins Lancaster, PA Scientist - Small Molecule Analytical Chemistry Master's degree in chemistry, pharmaceutical science, or other related degree concentration Exp: 1 year |
Eurofins' BPT Small Molecule Method Development and Validation team is seeking an Scientist to join their team full time in Lancaster, PA. This individual will work in a duel analyst and data reviewer role. | 04/07/2025 |
| 1384 | Evonik Birmingham, AL Microbiology Lab Technician Bachelor’s degree in microbiology, biological sciences, or related field of study Exp: 1 year |
This position is responsible for conducting routine microbiological testing, documentation, and data analysis, of utilities, raw materials, facilities and equipment. Additionally, the microbiology technician will be responsible for upkeep of the laboratory, laboratory supplies, and other various routine laboratory tasks. | 04/07/2025 |
| 1385 | Evonik Birmingham, AL Manufacturing Specialist BA/BS Degree in STEM subject Exp: 0-2 years |
The Manufacturing specialist acts as primary production process owner and subject matter expert (SME) for manufacturer of final products in Birmingham Labs, PDS Services. Responsibilities include managing procedures, batch documentation, data and information, reporting and analysis. Short term growth of staff working in assigned area and unit operations: assure technical knowledge, proficiency, and compliance is embedded as part of training, training material, GMP documentation, job aids, and others as needed. | 04/07/2025 |
| 1386 | Evonik Birmingham, AL Associate Scientist Bachelor’s degree in Chemistry or other relevant science Exp: 0-3 years |
This position is responsible for completing project tasks; and serving as the Quality Control contact on one or more projects by carrying out laboratory experiments, completing assignments that are varied in nature, contributing to report writing and representing SurModics at meetings with customers. | 04/07/2025 |
| 1387 | Evonik Bayport, TX Lab Technician I Bachelor's Degree in chemistry or related scientific or engineering fields. Exp: 1 year |
The Lab Technician will conduct analytical, chemical, and physical laboratory tests to assist scientists and engineers in making qualitative and quantitative analyses of solids, liquids, and gaseous materials for research and development of new products or processes, quality assurance and control, maintenance of environmental standards, and other work involving experimental, theoretical, or practical application of chemistry and related sciences. | 04/07/2025 |
| 1388 | Evonik Birmingham, AL Plant Engineer I BS/MS in an engineering field including but not limited to Mechanical, Electrical, Industrial, Chemical, or Biomedical Engineering Exp: 1-3 years |
The Plant Engineer I acts as system owner and subject matter expert (SME) for assigned area(s) to include but not limited to infrastructure, utilities, and process equipment. He/ She will ensure that the assigned systems are in a state of operational readiness by ensuring that preventive maintenance is carried out on time and in full, any issues are documented and investigated, corrective and preventive actions are implemented. He/ She provides technical expertise to maintain and continuously improve assigned areas to improve reliability, reduce downtime, minimize costs and ensure technical means for safe and high-quality operation. | 04/07/2025 |
| 1389 | Evotec Seattle, WA QA Specialist Bachelor's Degree in Biochemistry, Biology, Microbiology, Chemistry, or a Scientific/Engineering degree Exp: 1 year |
This role is responsible for the execution of day-to-day QA responsibilities for GMP manufacturing, along with building and enhancing the quality assurance systems. The role incumbent works both independently and collaboratively with Manufacturing, Quality and Facilities staff to ensure compliance with cGMPs and internal procedures. | 04/07/2025 |
| 1390 | Exact Sciences Madison, WI Metrology Associate I Bachelor’s degree in technology, electronics, mechanical engineering, computer science, Molecular Biology or related field Exp: 1+ years |
The Metrology Associate I will service custom and off-the-shelf laboratory instrumentation and equipment. This role will be responsible for, assembly, installation, calibration, routine maintenance, investigation and diagnosis of failures, repair, requalification, and filing service reports. The Metrology Associate I will work with colleagues to ensure proper instrument function and maintenance. | 04/07/2025 |
| 1391 | Exact Sciences Madison, WI Calibration Lab Technician I Bachelor’s degree in Electronics, Molecular Biology, or related field Exp: 1+ years |
The Calibration Lab Technician I is responsible for performing calibration, maintenance, and repair on a variety of equipment sent into the calibration lab (e.g., pipettes (single & multi-channel), bottle top dispensers, load cells, masses, timers, temperature measuring equipment, etc.). This role will demonstrate a high level of organization, the ability to multitask and build trust with internal and external customers. | 04/07/2025 |
| 1392 | Exactech Gainesville, FL Manufacturing Engineer Bachelor's degree Exp: 1-3 years |
Create and maintain the lowest cost, highest quality machining & manufacturing processes, tooling and supporting documentation for all parts produced. | 04/07/2025 |
| 1393 | Excellos San Diego, CA Cell Therapy Manufacturing Associate I or II Bachelor’s degree in cell biology or related field Exp: 1+ years |
The Manufacturing Associate I or II, Tissue and Cell Therapy is responsible for performing well regulated GMP aseptic cell culture activities including media preparation, cell thaws, cell expansion, cell harvesting, and cryopreservation using standard cell culture technologies in a cleanroom environment. The Associate will be responsible for following Batch Production Records, Standard Operating Procedures, and work instructions in manufacturing spaces. The Associate will be responsible for participating in the maintenance of critical supplies, equipment, product testing, product storage and product distribution. | 04/07/2025 |
| 1394 | EyePoint Watertown, MA Process Engineer I (Manufacturing) Bachelor of Science, Engineering Exp: 1-2 years |
EyePoint is seeking a motivated Process Engineer I with excellent interpersonal skills to join our team. This person will be responsible for process sustaining and improvement of all components, device and packaging related projects. This position requires the application of continuous improvement, equipment oversight, trending, layout plans, testing, data analysis and report writing to resolve and improve manufacturing efficiencies. Candidate must be able to effectively collaborate with internal R&D, Quality, Regulatory and Operations departments and with external vendors and suppliers to deliver against project timelines and maintain process sustaining activities. The ideal candidate possesses the ability to develop credibility and trust as a technical resource to contribute to the company’s growth, productivity, and innovation. | 04/07/2025 |
| 1395 | Flamma Group Malvern, PA Associate Process Scientist BS or MS in Organic Chemistry Exp: 0-1 years |
Execute laboratory experiments. Assist in determining operational space for various process parameters to ensure efficient and succesful scale up. Help evaluate safety of processes utilizing calorimetry data and stability data to fully understand the hazards and the trigger points of these hazards. Follow guidance from senior scientists or project leader to problem solve complex synthetic problems during development. Assist in scale up of processes in the kilo labs. Support scale up of processes in the pilot plant in a GMP environment. Collaborate with analytical chemists to complete work assignments. Contribute to laboratory organization. Accurately collect reliable data in the form of lab procedure or reports to be used for updates to customers or during drafting of production's MBR. | 04/07/2025 |
| 1396 | Fresenius Kabi North Andover, MA Engineer, Test (Medical Device) Bachelor’s degree in Engineering (Mechanical, Computer, Biomedical or related) Exp: 1-3 years |
The Engineer, Test (Medical Device) assists with all phases of systems performance verification and validation activities for infusion devices to support product development, product changes, and regulatory submissions. This includes prototype evaluations, planning, and execution of informal and formal verification cycles and reporting. | 04/07/2025 |
| 1397 | Fresenius Kabi Melrose Park, IL Packaging Engineer - Nights Bachelor’s degree in Engineering (Electrical, Mechanical, Automation, Controls, Computer, etc.) Exp: 1-3 years |
The Packaging Engineer will be responsible for using technical expertise in support of daily operations in packaging operations by defining, measuring, analyzing, coordinating, implementing and follow-up concerning projects and activities designed to increase or improve safety, quality, productivity, and/or capacity. Apply accepted engineering practices and project management techniques to assigned daily tasks and projects. Analyze situations, break them down into key components and milestones, conduct fact-finding missions, provide detailed plans of action, and implement plans as assigned. | 04/07/2025 |
| 1398 | Fresenius Kabi Melrose Park, IL Manufacturing Engineer Bachelor’s degree in Engineering (Electrical, Automation, Controls, Computer, Mechanical, etc.). Exp: 1-3 years |
The Manufacturing Engineer uses knowledge and technical expertise in support of daily operations within aseptic filling by defining, measuring, analyzing, coordinating, implementing and follow-up concerning projects and activities designed to increase or improve safety, quality, productivity, and/or capacity, all under guidance of Sr. Engineers or Production Management. Applies accepted engineering practices and project management techniques to assigned daily tasks and projects. Analyse situations, break them down into key components and milestones, conduct fact-finding missions, provide detailed plans of action, and implement plans as assigned. | 04/07/2025 |
| 1399 | Fresenius Kabi Wilson, NC Validation Engineer BS/BA degree in science, engineering, manufacturing technology or closely related field Exp: 1-3 years |
Responsible for providing technical support to operations in terms of equipment/system initial validation and equipment/system requalification’s. Will participate in equipment improvement teams charged with enhancing the compliance and performance of plant systems, while considering the regulatory requirements for change control. The individual must have a comprehensive understanding of cGMPs and become certified to enter Controlled Areas of the plant (Grade D, C and up to B/ A). The ability to write reports clearly, concisely and accurately; accurately record data and a basic understanding of statistical analysis is also required to perform these duties. Weekends and Off-shift hours are periodically required. | 04/07/2025 |
| 1400 | Fresenius Kabi Melrose Park, IL Scientist I B.S. in Chemistry, Biology or related physical science Exp: 1-4 years |
A Scientist I in Quality Control is responsible for an intermediate level of expertise in analytical chemistry, chromatographic methods of analysis and instrumentation, including troubleshooting. Directs and provides guidance to associate scientists. | 04/07/2025 |
| 1401 | Fresenius Kabi Melrose Park, IL Scientist, Analytical Development MS degree in Chemistry or related field Exp: 0-3 years |
The Scientist, Analytical Development conducts all aspects of Analytical Development including method development, experimentation, and record keeping. The incumbent must be able to develop and implement methods that meet project needs. The position is responsible for conducting analytical development studies with increasing complexity in nature and solving problems to ensure a robust method can be performed in the laboratory. | 04/07/2025 |
| 1402 | Freudenberg Carpinteria, CA Quality Engineer I - Inhealth Technologies Bachelor’s degree in Engineering, Sciences or related discipline Exp: 1+ years |
Reviews/ approves Design Control documentation (e.g. Design Verification, Process, or component validation), Leads Test Method validation activities associated with Design Verification activities, Represents Quality in New Product Development (NPD) project team meetings & Design Reviews, Prepares and releases Inspection Plans and Quality Control Inspection Criteria (QCICs) that supports qualification of purchased components, Audits Design & Development activities to ensure compliance with procedures and standards, Supports Risk Management activities for new or legacy products. This includes Risk Management Planning (RMP), Risk Analysis including post-market risk assessments, create Risk Management Reports, Leads complaint investigations and trend reporting for InHealth Technologies (IHT) products, Analyze internal and external quality product performance trends and address non-conformities, Represent Quality engineering in Engineering Change Order process for IHT products, Participates in both Internal and/or External audits, Participates in any product recalls or field actions | 04/07/2025 |
| 1403 | Freudenberg Jeffersonville, IN Manufacturing Engineer I Bachlors Degree in Technical Discipline (Mechanical, Manufacturing, Mechatronics or Biomedical). Exp: 1-3+ years |
Lead the identification, development, and qualification of manufacturing processes improvements. Deploy GROWTTH® tools to create simple, robust, and innovative manufacturing processes for new and sustaining products. Create and maintain quality system documentation such as process failure mode effects analysis, process flow charts, process validation plans, validation protocols, manufacturing procedures, etc. Supports the development and use of all production and control related processes and documentation including APQP, Control Plans, Qualification Plans, Engineering Change, Deviations, Corrective and Preventative Actions, DFMEA, PFMEA, PPAP, FAI, DFMA, and SPC tools. Identify and establish new processes and technologies necessary to achieve best cost targets. Provide coaching, and guidance regarding project tasks to other engineers, designers, technicians and associates. | 04/07/2025 |
| 1404 | Frontage Laboratories Exton, PA Associate Scientist Bachelor’s or master’s degree in Biochemistry, Molecular Biology, Immunology, Pharmaceutical Sciences, or a related field. Exp: Entry Level |
We are seeking a highly motivated and detail-oriented Associate Scientist to join our Pharmacokinetics (PK) group. The successful candidate will support bioanalytical method development, validation, and sample analysis using ligand binding assays (LBA) to assess pharmacokinetics for preclinical and clinical studies. This role requires expertise in bioanalytical techniques, data analysis, and regulatory compliance. | 04/07/2025 |
| 1405 | Contract Pharmacal Corp Hauppauge, NY Scientist I; Analytical R&D Bachelor’s or Master’s degree in chemistry or analytical chemistry Exp: 1-2 years |
Design and conduct routine laboratory analysis using various analytical instruments and software such as HPLC, UPLC, ICP, and UV-Vis. | 03/31/2025 |
| 1406 | Contract Pharmacal Corp Hauppauge, NY Chemist; Quality Control Bachelor’s degree in a science related field Exp: 1-9 years |
The Chemist is responsible for and has experience in performing chemical analysis for one of the assigned QC laboratories (Raw Material, Finished Product, Microbiology, ICP, Technical Support) which is responsible for the analysis and disposition of commercial materials (raw materials, finished product release, stability, validation, investigation), and environmental samples, as assigned, and documenting results in accordance with SOPs. | 03/31/2025 |
| 1407 | Contract Pharmacal Corp Hauppauge, NY Microbiologist; Quality Control Bachelor’s degree in a science related field Exp: 1-9 years |
The Microbiologist is responsible for and has experience in performing microbial analysis for the QC Microbiology laboratory which is responsible for the analysis and disposition of commercial materials (raw materials, finished product release, stability, validation, investigation), and environmental samples, as assigned, and documenting results in accordance with SOPs. | 03/31/2025 |
| 1408 | Cook Medical Winston-Salem, NC Sustaining Engineer MS in Engineering or Engineering Technology Exp: 1 year |
The primary purpose of this position is to lead projects to design, test and technically document design and/or process changes required for the maintenance of released medical devices. | 03/31/2025 |
| 1409 | Cook Medical Bloomington, IN Sterility Assurance Specialist I Bachelor's degree in Engineering, Microbiology, Biology, or related field Exp: 1-2 years |
The Sterility Assurance Specialist I at Cook Incorporated is responsible for multiple projects/tasks related to ensuring continued compliance with sterilization validation and product adoption requirements. The Sterility Assurance Specialist will collaborate on cross-functional teams to perform necessary tasks relating to product/process change evaluations, sterilization validations, product adoption, and assurance of sterility requirements. | 03/31/2025 |
| 1410 | Cook Medical Bloomington, IN Sr. Global Sustaining Engineer Bachelor's degree in Engineering, Microbiology, Biology, or related field Exp: 1-2 years |
Senior Engineer, Sustaining, will perform activities related to sustaining commercially available products. These activities may include (but are not limited to) product/process remediation, risk analysis, regulatory approval support, and product/process improvements. The Senior Engineer works independently with limited supervision on complex activities and projects. The Senior Engineer acts as a mentor and leader in the department and may review/approve the work of less experienced engineers and/or contractors. This is a Global Sustaining Engineering position. | 03/31/2025 |
| 1411 | CooperSurgical Livingston, NJ Laboratory Services Specialist II Bachelor’s or Master’s Degree in Biology or other related science Exp: 1 year |
Performs complex molecular-based procedures on clinical samples with a high degree of quality and in accordance with standard operating procedures. Analyzes clinical results and provides diagnoses. Communicates and collaborates with other professionals within the company and clients, as needed • Properly uses and maintains laboratory equipment. Performs clerical tasks associated with clinical cases, including but not limited to: maintenance of specimen and case logs, preparation/documentation of assay worksheets, preparation of analysis sheets and clinical reports. Receives and verifies clinical samples. Witnesses hands-on clinical procedures. Participates in lab maintenance (i.e. cleaning, annual/bi-annual/monthly maintenance of equipment, unpack supplies, etc.). Complies with Safety Standards and Good Lab Practices. Performs additional duties or assignments as directed by management. | 03/31/2025 |
| 1412 | CooperSurgical Los Angeles, CA Laboratory Technician II Bachelor's degree in Science Exp: 1-2 years |
Maintains demonstrated proficiency with all applicable Standard Operating Procedures. Performs semen evaluations to screen, process, and preserve for future clinical use. Execute an array of laboratory procedures including but not limited to: Daily setup of all laboratory equipment and daily QC. Intrauterine (IUI) and intracervical (ICI) insemination semen preparation. Sample Qualification- post-thaw sample analysis with both manual and automated analysis. Preparation of bodily fluid including blood, urine, and semen packing for specimen transport to reference laboratories. Cryogenic procedures including routine liquid nitrogen storage-tank verifications, internal vial transfers between tanks, vial quality control checks, preparing samples and shipping containers for vial movement. Conducts and accurately records all required daily, monthly and yearly quality control checks; responds with corrective action when needed. Communicates any errors, accidents or incidents to Management and records in associated tracking and record logs. Performs routine cleaning of laboratory equipment. Complies with all regulatory, quality assurance, quality control, standard operating, and safety procedures to audit-ready standards. Completes Bi-annual and annual proficiency and competency assessments. Participates in the review of standard operating procedures. Responsible for aliquoting and maintaining necessary aliquot-inventory levels for all media to maintain production. Responsible for lab supply maintenance. Performs all necessary opening and closing duties. Provides coverage for donor related tasks such as identification and qualification as needed. Always while ensuring privacy and maintaining the utmost professionalism. May perform phlebotomy if licensed. Other duties and projects as required. | 03/31/2025 |
| 1413 | Corden Pharma Boulder, CO QC Analyst - Temp Bachelor's Degree Exp: 1 year |
Performs all technician tasks accurately and efficiently without supervision. Initiates expert technical advice to customers and completes all tasks in the Technician Training manual. Maintains a high level of housekeeping and attention to detail. | 03/31/2025 |
| 1414 | Corden Pharma Boulder, CO QC Analyst - Days Bachelor's Degree Exp: 1 year |
Performs all technician tasks accurately and efficiently without supervision. Initiates expert technical advice to customers and completes all tasks in the Technician Training manual. Maintains a high level of housekeeping and attention to detail. | 03/31/2025 |
| 1415 | Corden Pharma Boulder, CO QC Analyst - Nights Bachelor's Degree Exp: 1 year |
Performs all technician tasks accurately and efficiently without supervision. Initiates expert technical advice to customers and completes all tasks in the Technician Training Manual. Maintains a high level of housekeeping and attention to detail. | 03/31/2025 |
| 1416 | Crown Bioscience San Diego, CA Research Associate, In vivo Bachelor's degree Exp: 6 months |
The purpose of the In Vivo Research Associate I position is to provide support on In vivo studies within the In Vivo Pharmacology group meeting Company's goals, objectives and quality standards. | 03/31/2025 |
| 1417 | CSL Schenectady, NY Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 03/31/2025 |
| 1418 | CSL Huntsville, AL Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 03/31/2025 |
| 1419 | CSL Portage, MI Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 03/31/2025 |
| 1420 | CSL Springfield, IL Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 03/31/2025 |
| 1421 | CSL Kankakee, IL QAO Specialist I B.A. or B.S. degree preferably in scientific or technical field (e.g., chemistry, biology, physics, engineering, computer science, technical writing) Exp: 0-2 years |
This is an entry level position into Quality Assurance Operations. Developing responsibilities include assisting with investigating deviations, relevant to area of responsibility. Responsible for driving continuous improvement on production floor to ensure compliance to cGMPs. Real time review of batch records, including critical processing steps with production floor presence. | 03/31/2025 |
| 1422 | CSL Waukegan, IL Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 03/31/2025 |
| 1423 | CSL Fairfield, CA Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 03/31/2025 |
| 1424 | Curia Springfield, MO Quality Control Analyst I Bachelor’s degree in Chemistry or related field Exp: 0-3 years |
The Quality Control Analyst I is responsible for performing routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished APIs, and stability samples. This role also participates in special projects, method development/transfers and cleaning study qualifications. | 03/31/2025 |
| 1425 | Curia Albuquerque, NM Microbiologist I Bachelor’s degree in a scientific discipline, preferably microbiology or related field Exp: 1 year |
The Microbiologist I is responsible for performing microbiological testing and quality activities to support product production, environmental monitoring, and product release in a pharmaceutical manufacturing environment. This role ensures compliance with regulatory requirements and company standards by conducting microbiological assays, analyzing trends, and accurately documenting and reporting results. The QC Microbiologist I collaborates with cross-functional teams to identify potential microbiological risks, troubleshoot deviations, and contribute to continuous improvement initiatives to maintain product quality and patient safety. | 03/31/2025 |
| 1426 | Cynosure Westford, MA Regulatory Specialist BS or BA in engineering or scientific field Exp: 1-2 years |
Responsible to be a Member of the Regulatory team that ensures regulatory approvals are effectively obtained and compliance with regulations is maintained. The specialist may participate in product development teams. Author regulatory submissions and technical files. Organize regulatory information and tracks and controls submissions. Review and advise on labeling for compliance with regulatory filings. Review product changes for impact on regulatory filings worldwide. Research regulatory issues and provides guidance and advice to colleagues. Review product complaints to determine if the events are reportable to regulatory agencies. | 03/31/2025 |
| 1427 | Dexcom San Diego, CA SW Development Engineer 2 Master's Degree in a technical discipline Exp: 0-2 years |
Our R&D team is looking for a Software Engineer with experience with data engineering, modeling and machine learning. In this role, you will design, develop, and deploy new data products leveraging a variety of data sources. You will also drive technical design, development and documentation of cross-functional and multi-platform capabilities. You will work in collaboration with data platform engineers, algorithm developers and clinical experts to focus on key metrics for diabetic patients and clinicians. To be successful in this position you will have experience in modern cloud-based systems (GCP, Terraform, BigQuery), development experience using standard modeling and machine learning libraries, understanding of container based platforms such as kubernetes. An essential part of our design involves utilizing PAAS components. | 03/31/2025 |
| 1428 | Dexcom San Diego, CA Process Development Engineer 2 Master's Degree in a technical discipline Exp: 0-2 years |
We are on the lookout for a top-tier Process Development Engineer 2 who brings a “can do” attitude and a desire for deep technical expertise in equipment, test design, statistics, and data analysis. As an integral part of our Engineering team, you will be instrumental in developing and fine-tuning manufacturing processes for medical devices, ensuring they are robust, efficient, and fully compliant with regulatory standards. Join us and make a significant impact on the future of medical technology! | 03/31/2025 |
| 1429 | Dexcom San Diego, CA Associate Facilities Engineer (HVAC, Plumbing and Electrical) Bachelor’s degree Exp: 0-2 years |
Join the Dexcom San Diego Facilities Engineering team where you will work closely with Manufacturing Operators and Innovators to provide planned and unplanned Facilities systems support. | 03/31/2025 |
| 1430 | Diacarta Pleasanton, CA Clinical Laboratory Assistant BS/BA in life science Exp: 0-1 years |
A CLA performs laboratory duties under the supervision of a licensed CLS. This position is for assisting the CLS and for sample processing, equipment operation and maintenance, and documents. | 03/31/2025 |
| 1431 | Dimension Inx Chicago, IL Research Associate/Engineer (In Vitro Stem Cells) Bachelor's or Master's degree in Biology, Cell/Molecular Biology, Biochemistry, Biomedical Engineering, Chemical Engineering, Chemistry, or related en Exp: Bachelor's: 1-3 years; Master's: 6 months-1 year |
The Research Associate/Engineer - In Vitro Stem Cells will play a key role in advancing Dimension Inx’s core platform technology and will work closely with the R&D and product development teams to conduct stem cell culture, in vitro testing, and biological assays to support new therapeutic product development to improve patient lives. The ideal candidate is a technically focused scientist or engineer with a background in cell biology, biomedical engineering, or related field, thrives in a rapidly changing, fast-paced environment, and has experience working on multiple and varied projects simultaneously. This position will report directly to a senior R&D team member. This role will contribute to the progression of collaborative early-stage R&D projects, the testing and development of new biomaterial and biological products, as well as various new product development projects. | 03/31/2025 |
| 1432 | Dimension Inx Chicago, IL Research Associate/Engineer (In Vivo & Histology) Bachelor's or Master's degree in Biology, Cell/Molecular Biology, Biochemistry, Biomedical Engineering, Chemical Engineering, Chemistry, or related en Exp: Bachelor's: 1-3 years; Master's: 0-1 years |
The Research Associate/Engineer - In Vivo/Histology will play a key role in advancing Dimension Inx’s core platform technology and will work closely with the R&D and product development teams to execute in vivo experiments, biological assays, and histological analyses to support new therapeutic product development to improve patient lives. The ideal candidate is a technically focused scientist or engineer with a background in cell and tissue engineering, biomaterials, or regenerative medicine, thrives in a rapidly changing, fast-paced environment, and has experience working on multiple and varied projects simultaneously. The position will report directly to a senior R&D team member. This role will contribute to the progression of collaborative early-stage R&D projects, the testing and development of new biomaterial and biological products, as well as various new product development projects. | 03/31/2025 |
| 1433 | Dimension Inx Chicago, IL Project Engineer (Materials) Bachelor's or Master's degree in Materials Science and Engineering, Chemical Engineering, Biomedical Engineering, Chemistry, Mechanical Engineering, o Exp: Bachelor's: 1-3 years; Master's: 0-1 years |
The Project Engineer - Materials will play a key role in advancing Dimension Inx’s core platform technology and will work closely with the R&D and product development teams to design, iterate, test, and produce materials for novel therapeutic products to improve patient lives. The ideal candidate is a technically focused engineer with a background in materials science or biomaterials, and thrives in a rapidly changing, fast-paced environment, and has experience working on multiple and varied projects simultaneously. The Project Engineer will report directly to the Lead Project Engineer. This role will contribute to the progression of collaborative early-stage R&D projects, the testing and development of new biomaterial and biological products, as well as various new product development projects. | 03/31/2025 |
| 1434 | DM Clinical Research Chicago, IL Administrative Research Assistant Bachelor’s degree in a healthcare-related field Exp: 1-2 years |
The Administrative Research Assistant plays a key role in providing administrative support to the clinical research team. This includes managing day-to-day operations, coordinating schedules, handling documentation, and ensuring smooth communication between team members, clients, and other stakeholders. The position requires a high level of organization, attention to detail, and familiarity with clinical research protocols and regulatory requirements. | 03/31/2025 |
| 1435 | DM Clinical Research Houston, TX PBMC Lab Technician Bachelor’s degree Exp: 1-2 years |
A PBMC Laboratory Technician will be responsible for conducting special laboratory procedures for clinical trials performing high complexity laboratory techniques including, but not limited to routine isolation of peripheral blood mononuclear cells (PBMC), or other laboratory procedures, etc., ensuring safety measures are followed by facilitating laboratory operations. | 03/31/2025 |
| 1436 | Eurofins San Diego, CA Asbestos PLM Analyst Bachelor’s degree in microbiology, biology, geology or a closely related science Exp: 1+ years |
The Analyst primarily performs analysis of bulk samples using PLM for asbestos. Analyst prepares and analyzes environmental samples according to scientific methodology in compliance with company Quality Assurance programs and SOP’s, and must be knowledgeable of both job-specific routine and complex analyses. The analyst validates and reviews data for accuracy, and enters laboratory data into the LIMS that ultimately generates required reports to clients. Schedules sample workload according to due dates and sample hold times, and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation. | 03/31/2025 |
| 1437 | Eurofins St. Louis, MO Associate Scientist - Analytical Assay Bachelors or Masters Degree in Biotechnology, Biochemical Engineering, Analytical Chemistry, Chemical Engineering or other related fields Exp: 1-3 years |
The position will be providing analytical support to biotherapeutic process development teams, specifically focusing on large molecules (proteins, polysaccharides, nucleic acids, etc.). Candidates should have familiarity with several of the below laboratory techniques; they should also possess expertise/knowledge with: Ultraviolet and visual light spectroscopy (UV-Vis), Analytical chromatographic separations using HPLCs or UPLCs, SEC-MALS, Small-volume multichannel pipetting skills and plate-based assays | 03/31/2025 |
| 1438 | Edwards Naperville, IL Engr I, Software Quality - Failure Analysis Master's Degree in Engineering or Scientific field Exp: No exp |
Many structural heart patients suffer from heart failure with limited options. Our Implantable Heart Failure Management (IHFM) team is at the forefront of addressing these unmet patient needs through pioneering technology that enables early, targeted therapeutic intervention. Our innovative solutions are not just transforming patient care but also creating a unique and exciting environment for our team members. It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. | 03/31/2025 |
| 1439 | Edwards Naperville, IL Engineer I, Field Services/Technical Product Support Bachelor's Degree in Electrical, Computer Science, Biomedical, Mechanical, or Reliability Engineering Exp: 1-2 years |
Troubleshooting advanced technical support issues in the field that are escalated by the customer support team. This will include the intake, investigation, documentation, and resolution of complaints and other field issues. | 03/31/2025 |
| 1440 | eGenesis Northwest, IN Quality Control Technician B.S./M.S. in Life Sciences or related field Exp: 0-3 years |
eGenesis is seeking an innovative Quality Control Technician to provide day to day technical support of eGenesis’ environmental monitoring program. In this position you will be responsible for hands on environmental monitoring sampling, testing, reporting and trending of eGenesis’ GMP manufacturing facility (Norwest Indiana). You will ensure activities are executed in a cGMP compliant manner and will work collaboratively on support of our contamination control program. The ideal candidate will be independently motivated, a strong communicator and demonstrate proficiency in regulatory compliance. This position will be an onsite position in Northwest, IN. | 03/31/2025 |
| 1441 | eGenesis Madison, WI Research Associate, Assisted Reproductive Technologies BS/MS degree in animal science, biology, or a related discipline Exp: 1-3 years |
eGenesis is seeking a Research Associate II/Senior Research Associate to join the Process Development team and contribute to projects in andrology, embryology and cell culture. In this role, you will have the opportunity to get hands-on training from experts in these areas. Daily activities include execution of experiments, recording of data into electronic notebooks, and collaborating with other members of the Process Development team. By improving the pig production process, we contribute to the xenotransplantation program of eGenesis. | 03/31/2025 |
| 1442 | Elekta San Jose, CA Associate Medical Device Engineer (Contract) Bachelor's Degree in BioMedical, Mechanical, or equivalent Exp: 6-12 months |
Engineers who are in an early career stage as an individual contributor and are developing their general knowledge and skills. This a contract position. | 03/31/2025 |
| 1443 | Element Biosciences San Diego, CA Senior Manufacturing Technician - Chemistry Bachelor of Science degree in biology, biochemistry, chemistry, molecular biology, or other related life science discipline Exp: 0-2 years |
We are seeking an experienced Senior Manufacturing Technician who will play a pivotal role in supporting the manufacturing and QC of reagent consumables for Element Biosciences. This will include synthesis, purification, and analysis of key intermediates. This is an incredible opportunity for someone who is passionate about making a difference and looking to further their career in the biotech industry. This role will report to our Associate Director, Consumables Manufacturingand will be a San Diego based (on-site)role. | 03/31/2025 |
| 1444 | Elephas Madison, WI Data Scientist Bachelor’s or Master’s degree in Biostatistics, Bioinformatics, Biomedical Engineering, Data Science, Computer Science, or related field Exp: 1-3 years |
Elephas is a Madison, WI based biotechnology start-up company working to build an instrument platform that will inform how clinicians treat cancer patients around the world. We are seeking a highly motivated Data Scientist to join our dynamic team of scientists and engineers developing a platform to predict a cancer patient’s response to immunotherapy. The successful candidate will be motivated to develop analytical, statistical and computational data science methods and deliver data discovery and insights in a fast-paced, collaborative and interdisciplinary environment. | 03/31/2025 |
| 1445 | Veracyte San Diego, CA Histology Associate Bachelor's Degree in life sciences Exp: 1-2 years |
The Histology Associate I primary responsibility is to assist histology with specimen processing in the clinical laboratory. This may include receiving specimens, ensuring accurate entry into the Laboratory Information System (LIS), and /or preparing samples for testing and analysis. The Histology Associate I is knowledgeable with, and is a resource for others within the laboratory, the use of equipment, databases, and software applications. Maintains flexibility regarding work schedule including section assignment. | 03/27/2025 |
| 1446 | Veracyte Austin, TX Specimen Processor Bachelor’s degree Exp: 0-2 years |
The Specimen Processor in this CLIA Laboratory is a critical member of the laboratory team, responsible for receiving, accessioning, and documenting specimens with precision. This role requires accurate data entry, proactive identification, and resolution of sample integrity issues. Flexibility in scheduling, including holidays and variable shifts, is essential to meet operational demands. | 03/27/2025 |
| 1447 | Veracyte San Diego, CA Research Associate, Product Development MS in Genetics, Biochemistry, Molecular Biology or a related scientific field Exp: 1+ years |
Veracyte is seeking an exceptional candidate for a full-time Research Associate in the Product Development team at our San Diego location. The Product Development team at Veracyte is tasked with developing high impact diagnostic assays to address unmet clinical need and improve patient outcomes. This on-site role will be primarily working in the San Diego laboratory supporting the Product Development team in achieving both short- and long-term goals and is a fantastic opportunity to gain hands-on, applied skills within an R&D team at an industry-leading diagnostics company. | 03/27/2025 |
| 1448 | Cabaletta Bio Philadelphia, PA Process Engineering Associate, Person-In-Plant Bachelor’s degree Exp: 1-2 years |
The Process Engineering Associate, Manufacturing Science and Technology (MS&T) is responsible for supporting clinical and commercial manufacturing production at Cabaletta’s cell therapy CDMO. This position will work very closely with manufacturing partners and requires frequent work onsite at manufacturing facility and occasional weekend and overtime work. | 03/27/2025 |
| 1449 | Cambrex Waltham, MA Associate Scientist BS or MS in chemistry Exp: 0-4 years |
Snapdragon Chemistry is currently seeking exceptional candidates for its Associate Scientist or Senior Associate Scientist position in Waltham, MA. A successful candidate will be joining a group of innovative and entrepreneurial scientists, with broad deliverables including the design of synthetic routes amenable to continuous flow processing, the development of reactor systems incorporating cutting-edge flow technology, and delivering intermediates, APIs and high value specialty chemicals to our clients. We are looking for a candidate who has a passion for working in a fast-paced, dynamic environment. The ideal candidate will have a BS or MS in chemistry with experience working in a chemistry research lab. The candidate should have experience in using kinetic analysis and other experimental tools to determine reaction mechanism and experience with typical analytical methods. Experience with the development of reactions in flow is preferred but not required. Candidates must possess strong written and oral communication skills. | 03/27/2025 |
| 1450 | Cambrex Durham, NC Scientist II (ARD) MS Chemistry Exp: 0+ years |
As a Scientist I (QC) in the Cambrex Analytical team, you will support a diverse range of client programs and be an integral team player within a highly cross-trained analytical core team. Execute analytical methods and provide general analytical support, such as release and stability testing of drug substances and drug products. Able to organize routine work independently and to evaluate, troubleshoot and interpret generated data. Demonstrated understanding of method development and qualification / validation principles. Routinely and effectively interacts with clients to discuss data and methods. Works on problems of moderate and sometimes advance scope in which analysis of situation or data requires a review of identifiable factors. Exercises judgment within defined procedures and practices to determine appropriate action. | 03/27/2025 |
| 1451 | Cambrex Charles City, IA Project Engineer BS in Engineering Exp: 1-3 years |
The Project Engineer performs general engineering duties for new installations and equipment, and modification of existing facilities and equipment. These duties are to be carried out with safety, efficiency and quality at the forefront. | 03/27/2025 |
| 1452 | Cambrex Longmont, CO Associate Scientist, Manufacturing BS in chemistry or related field Exp: 0-3+ years |
The Associate Scientist, Manufacturing will work within a team to perform kilogram scale organic synthesis of pharmaceutical drug substance. The Associate Scientist will operate chemical manufacturing equipment and execute detailed written instructions from a batch record under Good Manufacturing Practice (cGMP) conditions. In addition, the Associate Scientist is responsible for maintaining the manufacturing suites for activities by properly setting up, breaking down, operating, and cleaning production equipment for both GMP and non-GMP drug substance manufacturing operations. An Associate Scientist in manufacturing will operate under and develop subject matter expertise in cGMP practices and Good Documentation practices (GDP) within the Quality Management System. | 03/27/2025 |
| 1453 | Cambrex Marlborough, MA Clean Room Analyst - Microbiological Environmental Monitoring Bachelor’s degree or higher in Microbiology or related field Exp: 1 year |
Our Clean Room Services team is looking for both entry level and veteran Environmental Monitoring Analysts that are passionate about leveraging their talents to provide an outstanding customer experience. If you’re interested in receiving excellent training and working as part of a team of experts with opportunities for growth, you’ll be a great fit in our strong company culture. As a Cleanroom Services Analyst you will perform environmental monitoring and cleanroom qualifications within controlled environments. You will travel to regional client sites to provide your expertise with equipment, procedures, policies and regulations to ensure that their cleanrooms meet the requirements for safe manufacturing of medical devices, pharmaceuticals and other patient products. | 03/27/2025 |
| 1454 | Cambridge Isotope Laboratories Andover, MA Senior Chemist I Bachelor's or Master's degree in Chemistry or a related field Exp: 1-3 years |
Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Senior Chemist I based onsite in our Andover, MA facility. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. The Senior Chemist I will be responsible for the de novo synthesis, route development, and final product characterization of a wide variety of complex isotopically labeled targets (13C, 15N, 18O, and D isotopes). This role demands the production of high-quality, finished products in accordance with established specifications, while adhering to CIL’s safety and general policies. The Senior Chemist I will operate with a high degree of autonomy, ensuring that production requirements for safety, yield, time, and quality are consistently met. | 03/27/2025 |
| 1455 | Cambridge Isotope Laboratories Andover, MA Chemist, Deuterated Solvents and Reagents BS in Chemistry or related field Exp: 1-2 yeaers |
Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Chemist, Deuterated Solvents & Reagents based onsite in our Andover, MA facility. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. The Chemist, Deuterated Solvents and Reagents role will support the Solvents and Reagents group, under the supervision of a group leader or supervisor to execute chemical exchanges, enrichment, and purification of isotopically labeled solvents, products and materials utilizing highly detailed SOPs and procedures. They are also responsible for supporting continuous improvement projects on safety, quality, and productivity. | 03/27/2025 |
| 1456 | Capricor Therapeutics San Diego, CA MSAT Training Specialist Bachelor’s degree in a life science discipline (e.g., Biology, Biotechnology) Exp: 1-3 years |
We are looking for a dedicated and detail-oriented Training Specialist to join our team and drive excellence in our GMP manufacturing operations. In this position, you will play a critical role in designing, implementing, and continuously improving training programs for our Cell Therapy Manufacturing Team. You will help ensure that all personnel maintain a high standard of skill, knowledge, and compliance with GMP and regulatory requirements, ultimately supporting the safe and efficient production of our innovative therapies. | 03/27/2025 |
| 1457 | Capricor Therapeutics San Diego, CA Manufacturing Associate I/II Bachelor’s degree in Biomedical Engineering, Biological Sciences, or a related field. Exp: 1-3 years |
As a Manufacturing Associate, you’ll be a vital part of Capricor’s efforts in delivering therapies for patients in need. Supporting critical clinical trials and exosome development, you’ll perform meticulous production tasks and documentation to uphold our quality and compliance standards. This role places you in a cleanroom environment, where precision and attention to GMP standards are essential. You’ll be instrumental in ensuring that each production step is performed with accuracy, ultimately contributing to Capricor’s therapeutic success. | 03/27/2025 |
| 1458 | Capricor Therapeutics San Diego, CA Process Development Associate 2/3 Master's degree in a scientific discipline (e.g., biology, biotechnology, or related field) Exp: 0-2 years |
The Process Development Associate will play a key role in advancing Capricor’s biomanufacturing efforts by evaluating, improving, and scaling processes for therapeutic production. This position focuses on optimizing product yield, reducing costs, and ensuring scalability—from small experimental batches to large-scale manufacturing—while maintaining quality and efficiency. Reporting to the Process Development Director or Associate Scientist, the associate will collaborate with cross-functional teams to support the production of cell -based therapeutics, troubleshoot challenges, and implement innovative solutions. This role is ideal for a hands-on, detail-oriented professional eager to contribute to cutting-edge biotech advancements. | 03/27/2025 |
| 1459 | Capricor Therapeutics Los Angeles, CA Quality Assurance Associate 1 Bachelor’s Degree Exp: 1+ years |
Capricor is seeking a self-motivated team player with attention to detail, who enjoys organizing, making processes better, and making a difference in patient lives. The successful candidate will serve an essential role in supporting clinical product launch and production. This includes batch record review, deviation investigation, label issuance, and word processing, tracking, issuing, distributing, and archiving companywide GLP / GCP / GMP controlled documentation, training, and facility support systems. Knowledge of standard processes involved in document control and experience in an FDA regulated environment is required. The position will report to the Quality Assurance Supervisor. | 03/27/2025 |
| 1460 | Capstan Medical Santa Cruz, CA Manufacturing Engineer I-II BS or MS in related engineering discipline Exp: 1+ years |
The Manufacturing Engineer will have the exciting opportunity to join a growing team and work on developing and supporting manufacturing processes for our structural heart products. What you’ll do: Develop and support the manufacturing processes for a new heart valve implant, Assist in a transfer from R&D to Manufacturing through Clinical Use, Identify and act upon areas for manufacturing process improvement, Troubleshoot manufacturing issues and collaborate cross-functionally to implement corrective actions, Provide guidance and perform training to technicians and operators for manufacturing processes, Other responsibilities as determined by project need | 03/27/2025 |
| 1461 | Caris Life Sciences Phoenix, AZ Pathologist Associate I Bachelor’s degree in a chemical, biological, clinical or medical laboratory science Exp: 1+ years |
The Pathologist Associate is responsible for supporting and assisting the Pathology and Pathology Operations departments in their daily operations. This position will perform tasks needed to be completed in the day-to-day operation. This position also includes performing the tasks of Macrodissection and Microdissection. | 03/27/2025 |
| 1462 | Caris Life Sciences Phoenix, AZ Development Associate II Bachelor’s or Master's degree in a Molecular Biology, Molecular Genetics, Biochemistry, or related field Exp: 1 year |
The qualified candidate will be working in the Assay Development and Validation Department. The individual will play a critical role in supporting the development, validation, transfer, establishment and successful launch of new molecular assays, instrumentation, and methodologies into the clinical laboratory. Candidate will be responsible for assisting with planning, designing, and performing various laboratory experiments, documentation, reagents receiving, storing and tracking, data analysis, summarization and presentation, transfer of knowledge to other team members and to other departments, training clinical personnel, as well as additional functions fit for the position. Development Associates are expected to contribute both technically and intellectually to optimize quality and efficiency for Caris’ pipeline of development projects. | 03/27/2025 |
| 1463 | Cell Signaling Technology Beverly & Danvers, MA Lab Technician II BS/BA Degree in Chemistry or related science Exp: 1+ year |
The Lab Technician II - Buffer Prep position is primarily responsible for following standard operating procedures, with increasingly limited supervision and also as part of a team, to provide high quality chemical solutions, highly responsive service, and to perform a wide variety of basic laboratory tasks in support of CST's Production, Development, and Research laboratories. | 03/27/2025 |
| 1464 | Cellares Bridgewater, NJ Process Engineer (I, II, III) Bachelor’s or Master’s degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering, or a related field Exp: 0-4 years |
We are seeking an innovative and highly motivated Process Engineer on our MSAT team who will contribute significantly to establishing our IDMO Smart Factories. This position is focused on supporting the development and implementation of automated cell therapy manufacturing processes. You will work closely with the Process Engineering Lead and other cross-functional teams to execute, develop, design, optimize, and validate processes to ensure efficient, high-quality, scalable manufacturing solutions. This is a multidisciplinary role & this individual will interface across many parts of the company (with customers, scientists, researchers, and engineers) to develop the best solutions possible. Candidates should enjoy working in a fast-paced, mission-driven environment and be prepared to tackle a broad selection of challenges as the company grows. | 03/27/2025 |
| 1465 | Cellares South SF, CA Cell Therapy Manufacturing Specialist Bachelor’s Degree Exp: 1+ years |
We are seeking an innovative and highly motivated Cell Therapy Manufacturing Associate to join our Process Sciences team who will contribute significantly to the development and manufacture of our advanced cell therapy manufacturing platform. The primary focus of this position will be to support manufacturing operations, as well as day-to-day lab operations. This is a hands-on position that will train in Process Development, Analytical Development, and/or MSAT prior to joining the Manufacturing Group. Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows. | 03/27/2025 |
| 1466 | Cellares Bridgewater, NJ Cell Therapy Manufacturing Specialist Bachelor’s Degree Exp: 1+ years |
We are seeking an innovative and highly motivated Cell Therapy Manufacturing Specialist to join our Process Sciences team who will contribute significantly to the development and manufacture of our advanced cell therapy manufacturing platform. The primary focus of this position will be to support manufacturing operations, as well as day-to-day lab operations. Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows. | 03/27/2025 |
| 1467 | Centerline Biomedical Cleveland, OH Quality Engineer Bachelor's Degree in Engineering or related technical field Exp: 1-3+ years |
The Quality Engineer is an Exempt/Full-Time role responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 14971, ISO 13485:2016, MDSAP and FDA 21 CFR Part 820. This role supports supplier quality and monitoring primarily along with complaint/CAPA investigations, operations production and process controls, and product and service quality and the use of statistical techniques and other accepted quality principles. The Quality Engineer will also plan and execute activities concerned with the development, implementation, maintenance, and continuous improvement of Centerline’s quality systems. | 03/27/2025 |
| 1468 | Centrillion Palo Alto, CA Laboratory Technician B.A./B.S in a molecular biology, biochemistry, genetics, or microbiology Exp: 6 months |
We are looking for a Laboratory Technician to join our R&D team in Palo Alto. The role is part of a small group that divides their focus between innovative new projects and product development. The ideal candidate will be extremely organized, familiar with basic laboratory techniques, and excited to learn and grow within the team. Technicians will divide their time between hands-on laboratory work, data analysis, and lab organization and maintenance. Candidates with knowledge and experience of PCR, library preparation, NGS sequencing or RNA seq will be given preference. | 03/27/2025 |
| 1469 | Charles River Horsham, PA Formulations Technician I Bachelor’ degree (B.S.) Exp: 0-1 years |
Perform routine preparation of vehicles and test article dosage solutions for use in toxicology studies with close supervision. | 03/27/2025 |
| 1470 | Charles River Horsham, PA Research Assistant I – Analytical Chemistry Bachelor’s degree (B.A. / B.S) Exp: 0-2 years |
Generate and record data with minimal supervision in the performance of studies. Responsible for handling and processing samples and performing accurate data collection and reporting. Perform laboratory tasks by various basic methods. ESSENTIAL DUTIES AND RESPONSIBILITIES: • Perform basic laboratory procedures and collect and record/document research data in compliance with Good Laboratory Practices (GLPs), Standard Operating Procedures (SOPs), study protocols and company policies/practices. • Input, print and edit computer entries (e.g., laboratory data). • Prepare materials and data for shipment and archiving. • Receive samples and complete tracking documentation. • Review documentation of functions performed as part of quality control requirements. • Perform study preparation activities. • Maintain clean work areas. • Perform all other related duties as assigned. | 03/27/2025 |
| 1471 | Charles River Malvern, PA Technician I Microbiology Bachelor’s degree (B.A./B.S.) or equivalent in Biology or related discipline Exp: 0-1 years |
Responsible for performing daily laboratory tasks as they relate to Microbiology Testing Services. | 03/27/2025 |
| 1472 | Charles River Rockville, MD QC Associate I – Environmental Monitoring B.S in Biology or related field Exp: 1-2 years |
At Charles River Laboratories, we are looking for a highly motivated and energetic candidate to join our growing business in the CMO industry. The QC Analyst I will perform microbiological testing, static and dynamic viable and non-viable monitoring of classified clean room areas to support planned or in process manufacturing processes. This position, as well as all positions in the Charles River team will require demonstration of Charles River DNA “Characteristics and Behaviors” (Care, Lead, Own and Collaborate). | 03/27/2025 |
| 1473 | Charles River Ashland, OH Technician II, Formulations Bachelor’s degree (B.A./B.S.) Exp: No exp |
A Technician II will prepare basic to complex dosing material and samples for vehicles, solutions, suspensions, diets, and dispensations independently with some oversight. We are seeking an experienced Formulations Tech II for our Formulations Team at our Safety Assessment site located in Ashland, OH. | 03/27/2025 |
| 1474 | Charles River Ashland, OH Research Analyst I – Immunology Bachelor’s degree (B.A/B.S.) Exp: 0-2 years |
Perform laboratory tasks by various basic methods. Generate and record data with minimal supervision in the performance of studies. Responsible for handling and processing samples and performing accurate data collection and reporting. We are seeking a Research Analyst 1- for our Immunology team at our Safety Assessment site located in Ashland, OH. | 03/27/2025 |
| 1475 | Charles River Spencerville, OH In Vivo Technician I Bachelor’s degree (B.A./B.S.) in a biological science Exp: No exp |
A Technician I is in training to perform and become proficient in on-boarding tasks, procedures, and cooperating in a team environment. The technician is learning basic tasks required to conduct a study, which may include collecting and recording data in the performance of studies. Responsible for handling and restraining animals, clinical observations, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. The technician is working under close supervision to gain proficiency | 03/27/2025 |
| 1476 | ChemGenes Wilmington, MA Senior Research Support Associate B.S. degree in Biochemistry, Biology or related field Exp: 0-2 years |
Manufacture of synthetic DNA & RNA compounds. Assist with experiments supporting research in the synthesis of single-cell-barcoded beads, quality control of the synthesized beads, and performing experiments that include basic molecular biology techniques to sequencing experiments to validate and troubleshoot synthesis of DNA oligos to beads. Provide comprehensive technical support for scientists in the company; executing and optimizing ongoing experiments, analyzing results and designing follow-up experiments based on the results, and presenting findings and insights at group meetings. Evaluating research methods, procedures and techniques based on established objectives, conceiving and designing basic experimental protocols to ensure project completion in a timely fashion; recording and organizing data generated from the experiments in clear, concise, and assessable format; perform basic coding and statistical analyses; processing of in-vitro and in-vivo RNA for preparation of RNA-seq libraries for sequencing in Illumina platforms (Mi-Seq including Hi-seq and Next-seq). Experienced in techniques including but not limited to: running agarose gel, polyacrylamide gel electrophoresis, reverse transcription, quantitative PCR, fluorescent microscopy, flow cytometry; maintaining inventories of lab stocks. | 03/27/2025 |
| 1477 | ChemPacific Baltimore, MD Chemist, Deuterated Solvents and Reagents Master’s degree in Chemistry or Organic Chemistry Exp: 1 year |
Perform multi-step organic synthesis in solution and/or solid support: Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps such as extraction, recrystallization, silica gel column chromatography and LC/MS purification; perform cGMP synthesis of pharmaceutical ingredients; and perform process development and scale-up for kilogram quantities; and clearly record and communicate results and challenges to coworkers/supervisor. Equipments and tolls used included NMR, UV, MS and IR, Reactor (from 50ml to 221 to 10000l), vacuum pump, water aspirator, condenser, rotavap, voltage transformer, chromatography columns, TLC monitor, lyophilizer, separation funnel and addition funnel. | 03/27/2025 |
| 1478 | Cipla Central Islip, NY QC Chemist III Master of Science Degree Chemistry, Pharmaceutical Sciences, or related field Exp: 1 year |
Perform analytical testing for Raw Materials, Finished and In-Process of Drug Substances and Products like Related Compounds, Assay, Content Uniformity, Dissolution, Blend Uniformity, Karl Fischer Titration, and other related Physical testing for the methods using instruments HPLC, UV/VIS, Dissolution (USP-I, II & III) and FTIR. Execute Method validations of Drug Substance and Drug Products including Related Compounds, Assay, Dissolution, Content Uniformity, Blend Uniformity as per ICH guidelines/USP /FDA requirements. Collaborative team player with excellent communication skills working in a highly dynamic, cross disciplinary environment. Develop efficient and selective analytical procedures and draft/review laboratory SOPâ_x0080__x0099_s. Identify discrepancies, initiate, and investigate OOS/OOT results. Perform timely and accurate peer review of analytical test results report/document in notebooks. Maintain QC lab related systems to ensure compliance with industry standards. | 03/27/2025 |
| 1479 | Cipla Central Islip, NY QC Chemist II (DPI), Level 1 Bachelor's or Masters degree (BS or BA), physical sciences Exp: 0-3 years |
The job of the "Chemist" is simple described as an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory. The job itself may be further modified with respect to the department, group, etc., as exemplified in the "Department" on an individual assigned basis to a sometimes specific testing group. The role may be further modified based upon individual education, training, experience or a combination of all three. Generally, modifier designation with respect to experience for Chemist are as follows. However, combination of education, training, and special skills will determine the assignment of Level to a specific individual: | 03/27/2025 |
| 1480 | Cirtec Medical Lowell, MA Manufacturing Engineer I (Photolithography) Bachelor’s degree in engineering (STEM) Exp: 1-2 years |
This position is primarily responsible for developing and implementing robust cost-effective manufacturing processes and methods in accordance with product specifications within thin film fabrications. This position recommends and implements improvements to sustained production processes, methods and controls; as well as coordinates the launch of new products into pilot production. | 03/27/2025 |
| 1481 | Cleveland Diagnostics Cleveland, OH Associate Scientist- IVD Test Development Bachelor’s degree in Biology, Biochemistry, Molecular Biology, Biomedical Engineering, or a related field Exp: 1-4 years |
We are seeking a highly motivated Associate Scientist with experience or interest in in vitro diagnostic (IVD) assay development to join our dynamic team. The successful candidate will perform laboratory work, data analysis, under the guidance of a supervisor. This role requires hands-on execution of experiments, routine lab maintenance, and meticulous documentation to support product development, validation, and verification initiatives. The position involves handling human biological specimens, including blood, plasma, urine, and other bodily fluids, in compliance with all safety regulations and company policies. | 03/27/2025 |
| 1482 | Coastar Therapeutics San Diego, CA Research Associate II M.S. or B.S. degree Exp: 1-3 years |
Coastar Therapeutics is currently seeking a talented and highly motivated research associate with molecular biology background to join the multidisciplinary R&D team. The candidate will be responsible for designing and executing experiments in support of the biological membrane coated virus development. The candidate will also be involved in developing and validating collaborating projects to support Coastar’s fast-growing preclinical pipelines. The successful candidate must demonstrate broad and in-depth knowledge of molecular biology techniques. This is a full-time position reporting to the CSO and is located at our corporate headquarter in San Diego. | 03/27/2025 |
| 1483 | Color Health Burlingame, CA Clinical Lab & Fulfillment Associate (Temp Contract) Bachelor's degree in a relevant scientific field Exp: 1 year |
Color Health is revolutionizing cancer care with the nation’s first Virtual Cancer Clinic, delivering high-quality, physician-led multidisciplinary care across all 50 states. Our innovative, guideline-based approach spans cancer screening, risk assessment, prevention, diagnosis, treatment support, and survivorship. In addition to personalized direct medical care, our services include cancer genetics risk assessment, nutrition, mental health support and at-home cancer screening diagnostics. Using technology-driven, patient-centric solutions, Color is transforming how employers, unions, health plans, and governments address cancer. Color’s goal is to close critical cancer care gaps, improve cancer outcomes, and guide patients with empathy through their healthcare journeys. Color Health is seeking a Clinical Lab & Fulfillment Associate to support daily operations in our high-complexity CLIA-certified laboratory. This role will involve assisting with clinical testing, laboratory maintenance, and fulfillment operations to ensure seamless processing of biological specimens and timely distribution of testing materials. | 03/27/2025 |
| 1484 | Confluent Medical Technologies Laguna Niguel, CA Process Development Engineer I BS degree in engineering Exp: 0-3 years |
Confluent Medical Technologies is dedicated to working collaboratively with our customers, taking their projects from rapid prototype into high volume production. Our unparalleled technical expertise, proven experience and partnership with our clients has allowed us to perfect the process necessary to deliver world-class medical devices through innovative material science, engineering, and manufacturing. Our primary capabilities include: Nitinol components, balloon expandable stents and balloon catheters, delivery systems, biomedical textiles, access kits, and guidewires. We take pride in our position as the leader in the medical technology space and are driven by a passion to create products that our clients have envisioned for their customers. | 03/27/2025 |
| 1485 | BD Carol Stream, IL Quality Control Technician Bachelor's degree in related field Exp: 1 year |
The Quality Control Tech 2 works in the Quality Control department and performs general quality control quality assurance testing and review activities in accordance with current Good Manufacturing Practices (cGMP), company policy and safety regulations. | 03/16/2025 |
| 1486 | Bifrost Biosystems Berkeley, CA Mechanical Engineer BS or MS in Mechanical Engineering or a related field Exp: 0-4 years |
Are you passionate about pushing the limits of technology to advance our understanding of the life sciences? So are we! We’re looking for a highly motivated and experienced Mechanical Engineer to join a fast-paced start-up developing tools that will transform functional cell biology research. The ideal candidate will have strong engineering and problem-solving skills, a solid grasp of mechanical design fundamentals and some exposure to optical systems, microscopy and bio-engineering or biology. As Mechanical Engineer, you will be part of a small team designing, developing, specifying and testing Bifrost’s hardware products. Additionally, you will play a role in product definition, development and verification testing. | 03/16/2025 |
| 1487 | Abbott Temecula, CA Manufacturing Engineer Bachelors Degree Exp: 0-3 years |
Abbott Vascular provides innovative, minimally invasive and cost-effective products for treatment of vascular disease. Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents | 03/16/2025 |
| 1488 | Abbott Scottsdale, AZ Manufacturing Engineer I Bachelors Degree Exp: 0-3 years |
This position supports the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. This individual will work with supervisors, engineers, technicians, and operators to address problems and opportunities identified on manufacturing lines. He or she will be accountable for quality, safety, product output and yield initiatives, as well as providing line support on a daily basis. | 03/16/2025 |
| 1489 | Abbott Sylmar, CA Manufacturing Engineer I Bachelors Degree Exp: 0-3 years |
This position supports the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. This individual will work with supervisors, engineers, technicians, and operators to address problems and opportunities identified on manufacturing lines. He or she will be accountable for quality, safety, product output and yield initiatives, as well as providing line support on a daily basis. | 03/16/2025 |
| 1490 | Abbott Liberty, SC Manufacturing Engineer I Bachelors Degree Exp: 0-3 years |
This position supports the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. This individual will work with supervisors, engineers, technicians, and operators to address problems and opportunities identified on manufacturing lines. He or she will be accountable for quality, safety, product output and yield initiatives, as well as providing line support on a daily basis. | 03/16/2025 |
| 1491 | Abbott Minnetonka, MN Manufacturing Engineer I Bachelors Degree Exp: 0-3 years |
This position supports the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. This individual will work with supervisors, engineers, technicians, and operators to address problems and opportunities identified on manufacturing lines. He or she will be accountable for quality, safety, product output and yield initiatives, as well as providing line support on a daily basis. | 03/16/2025 |
| 1492 | Abbott Scottsdale, AZ Process Engineer Bachelors Degree Exp: 0-2 years |
This position works supports the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. Process Engineer performs analyses to develop design specifications and performance requirements. Provides technical information concerning manufacturing or processing techniques, materials, properties and process (advantages/limitations) engineering planning. Selects techniques to solve problems and make sound design recommendations. | 03/16/2025 |
| 1493 | Abbott Sylmar, CA Process Engineer Bachelors Degree Exp: 0-2 years |
This position works supports the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. Process Engineer performs analyses to develop design specifications and performance requirements. Provides technical information concerning manufacturing or processing techniques, materials, properties and process (advantages/limitations) engineering planning. Selects techniques to solve problems and make sound design recommendations. | 03/16/2025 |
| 1494 | Biocytogen Boston, MA In vivo Pharmacology Research Associate Bachelor’s or Master’s degree Exp: 1-5 years |
Biocytogen is a comprehensive research and discovery service provider for biotech and pharmaceutical industry and academic institutions. Its service platform integrates preclinical studies with innovative animal models, CRISPR-based gene editing, antibody discovery, and animal supplies, with current focus on immuno-oncology and oncology. We are looking for a highly motivated research associate with the ability to work both independently and in a collaborative manner. Biocytogen is a fast-growing company and has an abundance of opportunities available for you to grow your career. | 03/16/2025 |
| 1495 | BioMérieux Salt Lake City, UT Research Associate I Bachelor's degree in related field Exp: 6 months |
The Research Associate I (RA I) work to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g., nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to communicate and coordinate with peers and supervisor(s) effectively and respectfully. The position requires basic laboratory technical skills, organizational skills, attention to detail, critical thinking, troubleshooting and problem-solving, and a dedication to the mission and goals of the department and bioMérieux. A Research Associate I may receive general or detailed instruction and direct supervision on general work, new procedures, and assignments. | 03/16/2025 |
| 1496 | BioMérieux Philadelphia, PA Quality Engineer Masters’ degree in a life science or related field Exp: 1+ years |
The QA Engineer is responsible for supporting and facilitating the quality management system of the bioMérieux Philadelphia site. Under the guidance of the Quality Manager, the QA Engineer will work collaboratively with other departments including manufacturing, R&D, and purchasing to ensure compliance to the quality management system. Additionally, this position will assist in executing various site-wide quality projects and initiatives. The incumbent is responsible for monitoring site activities to ensure appropriate quality reporting and compliance to ISO9001:2015 standards. The QA Engineer will have a specific focus on supplier quality management, risk analysis of site processes, continuous process improvement, and sustaining quality management system activities. | 03/16/2025 |
| 1497 | BioMérieux Hazelwood, MO Final QC Microbiology Lab Tech Bachelor’s degree Exp: 0 years |
Using good aseptic lab practices, is responsible for supporting performance testing and physical inspections of finished good lots as well as internal use only lots through set up of VITEK2 cards, to completion. This position performs environmental testing and ensures proper documentation according to cGMP’s and current procedures, to completion. Performs all duties using safety conscious practices. Technician will uphold the lab attendance policy. | 03/16/2025 |
| 1498 | BioMérieux Philadelphia, PA PCR Technician 1 Bachelor’s degree in Biology or related field Exp: 0-2 years |
The PCR Specialist 1 is responsible for the formulation of highly complex PCR products and sub-solutions within the required timeframes and production schedules, in compliance with established Safety and Quality standards. They will be responsible for the proper handling and accurate pipetting of numerous different raw materials, combining 5-15 components into a final chemical formulation. Additionally, they will be responsible for the proper dispensing and labeling into final, customer facing formats. | 03/16/2025 |
| 1499 | Biogen Research Triangle Park, NC Manufacturing Associate - Biologics Bachelor’s Degree (STEM preferred) Exp: Entry Level |
Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; with two main areas/disciplines – Upstream (Cell Culture) and Downstream (Purification). MAs perform these critical steps within Current Good Manufacturing Practice (cGMP) biosafety cabinets and cleanroom suites. | 03/16/2025 |
| 1500 | Biogen Research Triangle Park, NC Manufacturing Associate II - Visual Inspection Bachelor’s Degree (STEM preferred) Exp: 6 months |
Manufacturing Associates perform processing steps and manufacturing support activities in our facilities in Research Triangle Park (RTP). These teams are the backbone of our operations – each person playing a critical role in delivering our therapies to the patients who need them. | 03/16/2025 |
| 1501 | BioMarin Novato, CA Lead, Manufacturing (Day Shift) BA/BS Exp: 1-2 years |
BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These individuals build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients. | 03/16/2025 |
| 1502 | BioMarin Novato, CA Lead, Manufacturing (Grave Shift) BA/BS Exp: 1-2 years |
BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These individuals build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients. | 03/16/2025 |
| 1503 | BioMarin Novato, CA Analyst, QC I Bachelor of Science degree Exp: 0-3 years |
Timely facilitation of incoming sample receipt and accessioning flow, decipher batch assignments across all assay types in accordance with agreed upon best practices. Execute microbiological and/or analytical methods to facilitate in-process testing under applicable cGMP guidelines, as well as contribute to the prompt reporting of results to meet the required timetables of internal customers. Perform environmental monitoring sampling and testing of facilities, equipment, and utilities. Evaluate completed assay validity, calculate and summarize results, analyze data per expected or specification ranges. Assist with the compilation and verification of trend analysis reports. Perform and collaborate with co-workers to appropriately share general housekeeping activity assignments, and ensure systems for laboratory maintenance are adequate for creating a consistent state of inspection readiness. Assist with monitoring and the control of laboratory supply and critical reagent inventories. Perform growth promotion of media and microbial identification testing. Qualify as trainer for specified methods, provide training to less experienced staff. Provide on call coverage to support oversight of QC laboratory equipment functionality. Exhibit proactive communication upon occurrence of compliance risks and deviations from laboratory procedures, perform initiation of investigation records within required timeframes. Provide input or assay support to the progression of test method validation, investigations, technical studies, and method transfer protocols. Attend team huddles and department meetings, generate ideas for laboratory infrastructure improvements and method optimization. Perform other responsibilities as deemed necessary. | 03/16/2025 |
| 1504 | BioMarin Novato, CA Research Associate 2, Drug Product Development DPDT MS in physical/Chemical/Biological/Life Science Exp: 0-2 years |
The Research Associate 2 role will support the team by generating high quality data while executing both routine testing and more complex, exploratory research projects. In addition, the candidate is expected to lead certain aspects of projects independently including experimental design, execution, interpretation of results, drafting of technical documents, and communication of data to stakeholders through oral presentations | 03/16/2025 |
| 1505 | Bionova Fremont, CA Sr. Manufacturing Associate BS in Life Sciences, or related discipline Exp: 0-1 years |
The Senior Manufacturing Associate will actively contribute to the manufacturing and technology transfer projects at the Bionova Scientific Fremont location. As part of the Purification/Manufacturing group, you will have opportunities to work on a wide-ranging set of projects for troubleshooting and investigations, system and workflow implementation, and tech transfers of processes into the GMP manufacturing facility. The role will provide hands-on execution of complex experiments in a team setting. The role will support GMP readiness and manufacturing activities. The scope of responsibilities may include but are not limited to Document writing (SOPs, Equipment URSs, etc.), equipment validation execution support and single-use assembly design. | 03/16/2025 |
| 1506 | Bio-Rad Woodinville, WA Quality Engineer I Bachelor’s degree in a related scientific discipline Exp: 0-2+ years |
Join Bio-Rad as our Quality Engineer and work in our Woodinville, WA site! Working in this Quality Assurance role, you will attend cross functional Daily Management meetings and represent Quality Assurance to address blocking issues and implement counter measures. You will manage the Material Review Board and ensure thorough data-driven documentation of non-conformities and risk based determination of CAPA. You will review data for trends, manage corrections and corrective action and support Global Supply Chain and business partners as requested. | 03/16/2025 |
| 1507 | Bio-Techne Minneapolis, MN Research Associate B.S. degree in Biochemistry, Chemistry, Biology, or a related field Exp: 0-2 years |
Performing routine quality control testing of stem cell products using protocol-defined assays to demonstrate their activity. The assays include culturing and handling of stem cells, primary cells, and basic cell lines for use in flow cytometry and immunocytochemistry (ICC). The position requires routine documentation, data analysis and good communication of results. Good Manufacturing Practice (GMP) documentation and workflow is required. Other duties include instrumentation maintenance, reagent preparation and routine lab support for QC antibody testing using western blot, simple wes and immunohistochemistry. | 03/16/2025 |
| 1508 | Bio-Techne Minneapolis, MN Research Associate - GMP Bachelor’s degree in biochemistry, biotechnology, or equivalent Exp: 0-2 years |
This position is responsible for purifying proteins and polyclonal/monoclonal antibodies in a GMP Lab, following GMP guidelines. This includes, but is not limited to GMP, ACFP, natural, and other products used by pharma and IVD customers. Purifies proteins and polyclonal/monoclonal antibodies by column chromatography, using a variety of techniques and equipment. Filter, aliquot, and bottling of product using aseptic techniques, and submits to bulk inventory. Documents batch records following GMP guidelines. | 03/16/2025 |
| 1509 | Bio-Techne Minneapolis, MN Quality Assurance Specialist Bachelor’s degree in Biology related disciplines Exp: 0-5 years |
The responsibilities of this position are label design and optimization, to perform internal audits, and to engage and support other Quality Assurance activities, including but not limited to, Supplier Management, Training Management, and Document Control. Perform additional duties as assigned. | 03/16/2025 |
| 1510 | Bio-Techne Minneapolis, MN Advanced Manufacturing Tech Bachelors science degree Exp: 1+ years |
The responsibilities of an Advanced Manufacturing Technician is to assist in the process of formulating buffers, diluents, and other components of Bio-techne’s best in class immunoassay products. Daily work may include recording data, operating equipment, product formulation and plate coating. Collaboration with other groups is also part of our work. Employees must have the ability to work independently and as a part of a team environment. Additionally, able to lift or move >50 lbs. routinely. | 03/16/2025 |
| 1511 | PSC Biotech Remote, Validation Engineer Bachelor's degree in related engineering discipline. Exp: 0-1 years |
This position will support system validation and product release processes, ensuring compliance with industry standards and regulatory requirements. You will play a key role in contributing to the development and improvement of validation procedures and driving overall product excellence. This is an entry-level, remote position. Successful candidates have a bachelor’s degree within an engineering discipline, a passion for technology, and exposure to system/software testing in the life science industry. | 03/16/2025 |
| 1512 | PSC Biotech York, PA Metrology Technician I Bachelor's degree in engineering or related technical field Exp: 0-1 years |
We are hiring an entry to junior level Metrology Technician responsible for conducting routine calibration tasks in alignment with established protocols and regulatory mandates. The position adeptly handles troubleshooting and equipment repair as needed, while ensuring the steadfast adherence to quality system compliance standards. | 03/16/2025 |
| 1513 | Bora Pharmaceuticals Camden, MA Analyst I, QC Analytical-2nd Shift B.S. in Chemistry or related field Exp: 0-2 years |
Perform analytical testing per cGMP in support of raw material, in-process, final product, stability. Typical hours are 10:00 pm – 6:30 am, Monday through Friday. Hours may vary to meet business and training needs. | 03/16/2025 |
| 1514 | Bora Pharmaceuticals Camden, MA Analyst II, QC Microbiology-1st Shift MS in Microbiology/Biology or related field Exp: 0-2 years |
The Analyst II, QC Microbiology position supports the Quality Control group at Bora Pharmaceuticals Camden Campus to maintain process optimization and manufacturing activities. The Microbiologist is responsible for performing activities in support of the Microbiology, Environmental Monitoring, and Utility testing programs, which includes microbiological product testing, monitoring of the manufacturing production space, and supporting quality initiatives. The individual routinely conducts monitoring, testing, and SOP generation and revision. | 03/16/2025 |
| 1515 | Bora Pharmaceuticals Camden, MA Analyst I, QC Microbiology-1st Shift BS in Microbiology/Biology or related field. Exp: 0-2 years |
Responsible for conducting qualitative and quantitative microbial analyses in support of environmental monitoring, cGMP manufacturing and stability of drug products and incoming raw materials. | 03/16/2025 |
| 1516 | Bora Pharmaceuticals Camden, MA Analyst I, QC Microbiology-2nd Shift BS in Microbiology/Biology or related field. Exp: 0-2 years |
Responsible for conducting qualitative and quantitative microbial analyses in support of environmental monitoring, cGMP manufacturing and stability of drug products and incoming raw materials. This position supports our 2nd-shift, working 2pm-10:30m, Monday through Friday. | 03/16/2025 |
| 1517 | BIB Southborough, MA Research Associate, Downstream Process Development BS degrees in biology, biochemistry, biomedical/biochemical engineering, or related fields Exp: 1+ years |
A Research Associate I is an entry level position for Bachelor’s degree with no prior experience and reports to a scientist level or above on relevant projects. The individual is responsible for routinely setting up, operating, and maintaining the downstream lab equipment under direct supervision at BIB. | 03/16/2025 |
| 1518 | Boston Scientific Arden Hills, MN R&D Engineer II - Electrophysiology MS in Mechanical or Biomedical Engineering Exp: 1+ years |
The engineer role will be a key team member in providing mechanical engineering support in the creation and development of new electrophysiology ablation catheter technologies. As R&D Engineer II, you will support new product development team solutions to multi-faceted customer issues. You will be a part of a high-performance team responsible for the design, implementation, and test of disposable medical devices within our electrophysiology pulsed field ablation single use device portfolio. This critical role will be a part of best-in-class development practices and rigorous, holistic product design in coordination with internal and external partners. | 03/16/2025 |
| 1519 | Boston Scientific Maple Grove, MN Quality Engineer II - Nitinol MS in engineering Exp: 1+ years |
The Quality Engineer II will be a key member of the Nitinol Shape Memory team supporting the self-expanding component product lines. This role will partner with representatives from the Manufacturing Engineering and Production functions. The person in this role will take the lead in addressing quality issues in a dynamic production environment. The ideal candidate will be comfortable interfacing with downstream internal customers and providing quality leadership to a production team running across 4 shifts. | 03/16/2025 |
| 1520 | Boston Scientific Maple Grove, MN R&D Sustaining Engineer II Master’s degree in Mechanical Engineering, Biomedical Engineering, or related field. Exp: 1 year |
As a R&D Engineer II, you will support commercial product improvement and supply continuity through design and material changes, product expansions, and complex problem solving. This role involves working collaboratively with cross-functional teams to ensure product designs meet the highest quality and regulatory standards. | 03/16/2025 |
| 1521 | Boston Gene Waltham, MA Laboratory Technician, Biospeciman Services Bachelor’s degree in Biological or Life Sciences Exp: 1 year |
The Laboratory Technologist will be responsible for pre-analytical accessioning, processing, and maintaining inventory of clinical blood samples in accordance with established laboratory procedures. This role ensures the integrity of patient samples, supports downstream users in clinical and research operations, and maintains compliance with laboratory quality and regulatory standards. | 03/16/2025 |
| 1522 | Bristol Myers Squibb Devens, MA Senior QC Microbiology Associate, Lab Operations BS/BA in?Biological, Chemical/Life Sciences Exp: 1-2 years |
To perform QC testing in support of bulk drug substance manufacturing using defined methods in a GMP-compliant laboratory. Ensures test results are accurately recorded, and abnormal data or equipment/instrument malfunctions are properly reported and escalated to management | 03/16/2025 |
| 1523 | BWX Technologies Erwin, TN Engineer 2 -- Fuel Dev & Variability Reduction MS. Degree -- Engineering. Exp: 1 year |
Evaluates situations, selects and applies standard engineering techniques, procedures and criteria, using judgment in making minor modifications. Assignments have a clear objective and require planning and investigation of limited number of possibilities. Work is reviewed for application of sound judgement and compliance with contract technical requirements and meeting of Division policies and procedures. Receives instructions on specific assignment objectives, complex features and possible solutions. Assistance is furnished on unusual problems and work is reviewed for application of sound professional judgment. | 03/16/2025 |
| 1524 | BWX Technologies Barberton, OH Metallurgical Engineer Bachelor or Master of Science Degree in Metallurgical Engineering, Materials Science & Engineering or Welding Engineering Exp: 1 year |
Provide technical leadership and utilize a background in materials for broad metallurgical support in a project team environment. Candidate will operate metallographic equipment for investigative purposes and communicate closely with others. Prepare, analyze and generate reports for the acceptance of metallographic specimens, primarily welded assemblies, but also includes determination of intergranular attack (IGA), plating thickness, EDM/laser recast layers, grain size, and general microstructural characterization to other specifications and in support of investigations. The candidate will be expected to have the ability to support or lead material-related investigations, develop laboratory best practices/standard procedures and manage metallurgical supply inventories. The ability to lead technical projects/investigations, manage documentation and time management skills are crucial. Familiarity with materials processing (i.e. melting, forging, heat treating, casting, welding, etc.), mechanical testing, metallography, EDM, plating, corrosion, and nuclear-grade materials is strongly desired. | 03/16/2025 |
| 1525 | Shimadzu Central Islip, NY Field Service Technician Associates EE or Bachelors Chem Exp: 1 yr |
Provide daily repair and maintenance support for assigned products; Conduct in-house bench repairs as needed while primarily handling field service calls with limited supervision; Travel within the local region (including day and overnight trips) to support customer needs; Offer technical support via phone to customers and field personnel regarding repairs, maintenance and installations. | 03/13/25 |
| 1526 | BioPharmGuy Anywhere, US Contract Data Work some college Exp: 0 yrs |
We are looking for someone with expertise in classifying diseases/conditions by medical specialty. Contract work on a task basis. Must be able to accept payment by PayPal or Venmo. Send us a message through the contact form if interested. | 03/12/2025 |
| 1527 | Arrowhead Pharmaceuticals Madison, WI Associate Scientist, Small Scale Synthesis B.S. Chemistry or Biochemistry degree Exp: 0-2 years |
Arrowhead Pharmaceuticals is seeking an Associate Scientist to join the Discovery Chemistry Department. The successful candidate will primarily focus on oligonucleotide synthesis, purification, analytical chemistry, and contributing to specific program goals. The Associate Scientist will be joining a team of highly motivated and experienced scientists and will contribute to the success of Arrowhead programs. | 03/10/2025 |
| 1528 | Arthrex Naples, FL Research Operations Specialist Bachelor’s or Master's degree Exp: 1 year |
Manages with autonomy and independent judgement the daily activities of the Department of Orthopedic Research that supports critical operations and functions. Responsible for departmental strategic development and surgeon collaborations. Spearhead key inter- and intra-departmental initiatives. | 03/10/2025 |
| 1529 | Artivion Austin, TX Associate Regultory Affairs Specialist Bachelor's degree in relevant science Exp: 0-2 years |
The Associate Regulatory Affairs (RA) Specialist is responsible for assessment of device and tissue product changes for regulatory implications and for performing regulatory activities in support of implementing these device changes (e.g., labeling and quality system implementation). The Associate RA Specialist is also responsible for supporting activities related to PMA annual reports, Canadian license renewals and maintaining required facility and state licensing/registrations. Additionally, the Associate RA Specialist will provide regulatory labeling support to ensure labeling compliance. The Associate RA Specialist will work independently with management oversight. | 03/10/2025 |
| 1530 | Associates of Cape Cod East Falmouth, MA Quality Control Analyst I B.S. degree in a relevant scientific discipline Exp: 0-2+ years |
Performs chemical and/or biological assays of commercial product raw materials, production intermediate and bulk samples, finished product, environmental monitoring samples, process and cleaning validation samples. Assays are qualitative, quantitative and investigational in nature and are performed in compliance with current Good Manufacturing Practices, Associates of Cape Cod Standard Operating Procedures, compliance guidelines of the FDA and other regulatory bodies, and approved license requirements. Learns and executes defined QC tasks efficiently and consistently. Results are compared to specifications and documented in a timely manner. Analyst has working knowledge of relevant QC techniques, policies and procedures to perform QC tasks and document results. Analyst receives minimal supervision on routine assignments and detailed instructions on new assignments. | 03/10/2025 |
| 1531 | Associates of Cape Cod East Falmouth, MA Quality Control Analyst II M.S. degree preferred in a relevant scientific discipline Exp: 0-2+ years |
Performs chemical and/or biological assays of commercial product raw materials, production intermediate and bulk samples, finished product, environmental monitoring samples, process and cleaning validation samples. Assays are qualitative, quantitative and investigational in nature and are performed in compliance with current Good Manufacturing Practices, Associates of Cape Cod Standard Operating Procedures, compliance guidelines of the FDA and other regulatory bodies, and approved license requirements. Results are compared to specifications and documented. Analyst has mastered most or all of the fundamental quality control concepts as well as some specialized technologies and receives minimal supervision on routine assignments. Analyzes and interprets test results independently and contributes to design of new studies in consultation with Supervisor. May provide guidance and training to more junior staff members. | 03/10/2025 |
| 1532 | AstraZeneca Mount Vernon, IN PET Formulation - Process Engineer Bachelor’s degree required, preferably in Science, Chemical Engineering, or other related technical discipline Exp: 0-1 years |
Are you ready to break new ground and leave a collective legacy? As a PET Formulation - Process Engineer, you will provide technical support for process manufacturing, investigating and correcting process-related problems and deviations from standards. This role offers the opportunity to play a pivotal part in evolving our Supply Chain, reimagining how we do things, and creating a lasting impact. | 03/10/2025 |
| 1533 | AstraZeneca Frederick, MD Quality Control Analyst Bachelor’s degree required, preferably in Science, Chemical Engineering, or other related technical discipline Exp: 0-5 years |
As a Quality Control Analyst, you will be responsible for conducting raw materials, in process, finished product, and stability testing according to standard operating procedures. You will complete appropriate documentation supporting testing procedures, including data capture forms, equipment logbooks, and inventory forms. You will also identify and troubleshoot equipment problems, enter data evaluated for compliance to specifications and report abnormalities. You will own minor deviations and simple change control and CAPA records. You will also support preparation of validation protocols, execute experiments, and provide data for validation reports. | 03/10/2025 |
| 1534 | AstraZeneca Waltham, MA Scientist, Oncology Bioscience MS in Biology, Oncology, Biochemistry, Pharmacology, Immunology or a related field Exp: 1+ years |
Would you like to apply your expertise to impact drug development in a company that follows the science and turns ideas into life-changing medicines? Then employment at AstraZeneca might be the right choice for you! We are seeking a highly motivated Scientist in Oncology Targeted Discovery with strong scientific and technical expertise in oncology research and a track record of scientific excellence to join our team in Waltham, MA USA. As a Scientist in our Oncology R&D department, you will be a key member of a team focused on supporting oncology projects through the drug discovery and development process. You will bring your theoretical and practical expertise in cancer biology to establish assay systems and deliver datasets that will have a direct impact on targeted therapeutics. | 03/10/2025 |
| 1535 | Bio-Techne Minneapolis, MN Research Associate B.S. degree in Biochemistry, Chemistry, Biology, or a related field Exp: 0-2 years |
Performing routine quality control testing of stem cell products using protocol-defined assays to demonstrate their activity. The assays include culturing and handling of stem cells, primary cells, and basic cell lines for use in flow cytometry and immunocytochemistry (ICC). The position requires routine documentation, data analysis and good communication of results. Good Manufacturing Practice (GMP) documentation and workflow is required. Other duties include instrumentation maintenance, reagent preparation and routine lab support for QC antibody testing using western blot, simple wes and immunohistochemistry. | 03/10/2025 |
| 1536 | Bio-Techne Minneapolis, MN Research Associate - GMP Bachelor’s degree in biochemistry, biotechnology, or equivalent Exp: 0-2 years |
This position is responsible for purifying proteins and polyclonal/monoclonal antibodies in a GMP Lab, following GMP guidelines. This includes, but is not limited to GMP, ACFP, natural, and other products used by pharma and IVD customers. Purifies proteins and polyclonal/monoclonal antibodies by column chromatography, using a variety of techniques and equipment. Filter, aliquot, and bottling of product using aseptic techniques, and submits to bulk inventory. Documents batch records following GMP guidelines. | 03/10/2025 |
| 1537 | Bio-Techne Minneapolis, MN Quality Assurance Specialist Bachelor’s degree in Biology related disciplines Exp: 0-5 years |
The responsibilities of this position are label design and optimization, to perform internal audits, and to engage and support other Quality Assurance activities, including but not limited to, Supplier Management, Training Management, and Document Control. Perform additional duties as assigned. | 03/10/2025 |
| 1538 | Bio-Techne Minneapolis, MN Scientific Support Specialist Bachelor’s degree in laboratory science or equivalent Exp: 0-2 years |
Provides high level technical support to customers on use of hematology products. Answers and documents incoming technical inquiries and complaints by phone and email on product techniques, procedures and troubleshooting. Communicates to obtain all pertinent information relating to the inquiry. Provides adequate information to problem solve or to assist in the resolution of the issue. Documents information and recurring technical issues to support product quality programs and product development. Works on complex problems of diverse nature where analysis requires in-depth evaluation of various factors. Supports the Marketing and Sales Departments. Provides guidance and recommendations on products based on customer needs and utilizes customer interactions to improve business opportunities. Collaborate with cross-functional teams for root cause analysis. Helps to identify gaps and collaborates to devise and implement process improvements. Assure a high level of quality and accuracy in the processing of customer QC data. Provide QC program support for OEMs, International Distributors and end-user customers. Follows company policies and practices as outlined in the Handbook and follows guidelines regarding safety as outlined in the AWAIR, Chemical Hygiene and Exposure Control manuals in accordance to the job. | 03/10/2025 |
| 1539 | Avance Biosciences Houston, TX Laboratory Associate II Bachelor’s degree in biological sciences Exp: 1 year |
Carry out Molecular Biology, Microbiology, Protein experiments following established SOPs and/or guidance of laboratory management. Perform DNA/RNA extraction, quantification, and gel QC. Perform PCR setup for qualitative and quantitative analysis. Report experimental results to project managers in a timely manner. Follow established quality management policies and GLP and GMP practices. | 03/10/2025 |
| 1540 | Avanos Medical Alpharetta, GA R&D Professional I Bachelor of Science in Biomedical Engineering or Mechanical Engineering Exp: 0-2 years |
The Research and Innovation (R&I) department will be focused on supporting efforts to grow the Digestive Health Enteral Feeding medical device business. This role requires a professional with entry level experience in Research and Development or New Product Development to deliver on the product development roadmap growing Avanos’ enteral feeding business. This candidate must support technical teams for design, development and implementation of changes and improvements to existing products within Avanos’ Digestive Health Business. | 03/10/2025 |
| 1541 | Avantor Sciences Irving, TX Project Engineer 1 Bachelor’s degree in Mechanical, Electrical, or Chemical Engineering Exp: 1-3 years |
The Project Manager will own project assignments from concept to closure. This will include preparatory documentation, stakeholder engagement, Scope of Work creation, cost estimation, schedule creation, solicitation of funding approvals, procurement activities, construction management, equipment qualification and validation activities, all in a ISO9000, FDA, AS9100, cGMP, ITAR environment. Other activities may be required or assigned depending on the specific project needs. Non-project-related work may include departmental documentation, participation in various initiatives as a team member or Subject Matter Expert, or collaboration with other departments and sites. | 03/10/2025 |
| 1542 | Avid Bioservices Tustin, CA Manufacturing Associate Support Bachelor’s degree with an emphasis in biology or chemistry highly preferred. Exp: 1+ years |
The Manufacturing Associate Support provides support for: Production Operations and multiple aspects of cGMP contract cell culture manufacturing in strict compliance with cGMP, under Standard Operating Procedures in a multi-product manufacturing facility, including, but not limited to production, documentation, writing reports, requesting and purchasing materials, and scheduling equipment services and calibrations. The Manufacturing Associate will play an integral role in ensuring the production and on-time release of quality products. The Manufacturing Associate will conduct themselves in a manner representing the core values (Integrity, Adaptability, Innovation, Teamwork, and Passion) of the company with the common purpose of improving patients’ lives by consistently delivering high-quality biopharmaceutical products. | 03/10/2025 |
| 1543 | Avid Bioservices Tustin, CA Manufacturing Associate, Downstream Bachelor’s degree with a preference for biology or chemistry emphasis. Exp: 1-2+ years |
Join our dynamic team as a Manufacturing Associate, Downstream! In this role, you'll be a crucial part of our multi-product manufacturing facility, working in strict compliance with cGMP and Standard Operating Procedures. Your responsibilities will encompass various tasks, including production, meticulous documentation, report writing, materials procurement, and equipment scheduling. You'll be instrumental in ensuring the timely production and release of top-quality products. At our company, we value core principles such as Integrity, Adaptability, Innovation, Teamwork, and Passion, all united by a shared mission to enhance patients' lives through the consistent delivery of high-quality biopharmaceuticals. If you're ready to make a meaningful impact, apply now and be part of our journey! | 03/10/2025 |
| 1544 | Avid Bioservices Tustin, CA Research Associate, Process Development - Downstream B.S. degree in a Biological Science. Exp: 1-2 years |
The Research Associate, Process Development Downstream will provide laboratory support for Process Development by assisting in the downstream process and/or method development. The Research Associate may be assigned various tasks within the department and outside the department as needed. | 03/10/2025 |
| 1545 | Avid Bioservices Tustin, CA Research Associate, Process Development Upstream B.S. degree in a Biological Science. Exp: 1-2 years |
The Research Associate in Process Development - Upstream will develop and optimize scalable cell culture processes and contribute to transferring the process to Avid Manufacturing. In addition, the Research Associate will maintain production equipment and will research and implement new methods and technologies to enhance process operations. | 03/10/2025 |
| 1546 | Avid Bioservices Tustin, CA Associate Specialist, Quality Assurance B.A. or B.S. degree (preferably in Life Science). Exp: 1+ years |
As an Associate Specialist, Quality Assurance, you will be a critical part of ensuring top-notch quality for our products and services. You will be responsible for various administrative tasks associated with Avid's electronic document management and training systems, issuing, and reconciling equipment logbooks and laboratory notebooks, and providing both formal and informal training to coworkers on relevant processes such as quality systems, training, and GMPs. | 03/10/2025 |
| 1547 | Axogen Vandalia, OH Quality Analyst Bachelor’s Degree in a Life Science discipline, engineering, or in a related field Exp: 0-2 years |
The Quality Analyst I performs quality control (QC) inspection and disposition of materials and products according to specifications. This role will perform QC inspection using measuring instruments (when applicable) and inspection methods. The role ensures any non-conforming materials or products that are identified are managed according to Axogen’s Quality System. The Quality Analyst is responsible for following all Axogen policies and procedures to ensure compliance with applicable FDA, state OSHA, and ISO regs and standards. Employees within this role will perform a variety of tasks under limited supervision. | 03/10/2025 |
| 1548 | B. Braun Medical Daytona Beach, FL QC Lab Tech II-Microbiology Bachelor's degree in relevant science Exp: 1-2 years |
Performs a variety of quality control tests on products at various stages of the production process to ensure compliance with quality and reliability standards. Records statistical data. Analyzes data and writes summaries to validate or show deviations from existing standards. Recommends modifications to existing or suggests new, standards, methods and procedures. | 03/10/2025 |
| 1549 | BA Sciences Salem, NH Analytical Chemist I Bachelor’s degree in Chemistry or a related science discipline Exp: 0-2 years |
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and BA Sciences. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. | 03/10/2025 |
| 1550 | BA Sciences Salem, NH Microbiologist QC I BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The QC Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and BA Sciences. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 03/10/2025 |
| 1551 | BA Sciences Salem, NH Microbiologist I – Environmental Monitoring BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The EM Microbiologist I conducts quantitative and qualitative analysis of pharmaceutical industries Environment according to FDA, ISO, cGMP and BA Sciences. Standard Operating Procedures. Duties will include Sampling of pharmaceutical industries through ISO standards and client specific test protocols. | 03/10/2025 |
| 1552 | Bachem Vista, CA Chemist Bachelor’s degree in chemistry or related scientific field Exp: 0-2 years |
The Chemist function is to work in a cGMP regulated environment manufacturing active pharmaceutical products (APIs) as well as performing related activities at Bachem. | 03/10/2025 |
| 1553 | Bachem Torrance, CA Chemist Bachelor’s degree in chemistry or related scientific field Exp: 0-2 years |
The Chemist function is to work in a cGMP regulated environment manufacturing active pharmaceutical products (APIs) as well as performing related activities at Bachem. | 03/10/2025 |
| 1554 | Balt Irvine, CA Manufacturing Engineer Bachelor’s degree in engineering or related field Exp: 1 year |
This fast-paced position will be responsible for the support and continuously improve current manufacturing process, through technical and process innovation for the manufacture of neurovascular medical devices that save patient lives. | 03/10/2025 |
| 1555 | Baxter Medina, NY Manufacturing Engineer Bachelor’s degree in engineering Exp: 1-3 years |
This description outlines the employment prerequisites and job responsibilities for the position of Manufacturing Engineer within the Continuous Improvement Team. Provide support in the execution of the site’s operational optimization and quality improvement projects to achieve Medina Plant goals and objectives. Drive/support various quality improvement, business continuity/expansion, and cost reduction initiatives from identification through implementation while working with cross functional resources to ensure results are achieved in a timely manner. | 03/10/2025 |
| 1556 | Baxter Marion, NC Associate II Quality Lab Chem FN Master’s Degree in Natural Sciences Exp: 0-3 years |
Conduct qualitative and quantitative chemical analysis on raw materials, solutions, and components following approved Standard Operating Procedures and test methods in an accurate and timely manner. Ability to work under minimum supervision while meeting deadlines. | 03/10/2025 |
| 1557 | Baxter Round Lake, IL Senior Electrical Engineer - R&D Masters in Electrical or Electronics or related Engineering Exp: 1+ year |
As the Sr. Electrical Engineer, you will develop creative solutions to challenging problems associated with the design of our new and existing infusion system product portfolio. You will possess strong technical capabilities, an excitement and energy for product development, and a passion for their work and the impact it has on saving and sustaining the lives of patients. | 03/10/2025 |
| 1558 | Baxter Marion, NC Quality Lab Associate I - Endotoxin Master’s Degree in biological sciences Exp: 0-3 years |
Conduct microbiological analysis on raw materials, solution, and water samples following approved Standard Operating Procedures in an accurate and timely manner. | 03/10/2025 |
| 1559 | Baxter Marion, NC Quality Lab Associate II - Endotoxin Master’s Degree in biological sciences Exp: 0-3 years |
Conduct microbiological analysis on raw materials, solution, and water samples following approved Standard Operating Procedures in an accurate and timely manner. | 03/10/2025 |
| 1560 | Baxter Hayward, CA Tech III, MNF Formulation Bachelor’s degree Exp: 6 months |
The Manufacturing Technician III is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Manufacturing Technician III is expected to fully participate in both departmental projects and any quality working teams which may be applicable. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. Manufacturing Technician III has sufficient technical and administrative competence to organize and lead production activities, including demonstrating leadership in state-of-the-art cGMP compliance, and environmental health and safety skills. | 03/10/2025 |
| 1561 | Baxter Marion, NC Engineer I, Project Engineering B.S.in Engineering Exp: 0-1 year |
We are looking for an individual to support a highly automated facility in North Cove, North Carolina. As a member of the Engineering department, the role will provide technical expertise to support plant manufacturing processes as well as other departments within the plant. In this role, you will focus on the implementation and adaptation of existing technologies of automation and associated processes in a manufacturing environment. The successful candidate must be a self-starter willing to assist the production and production service teams with hands-on troubleshooting. | 03/10/2025 |
| 1562 | Bausch + Lomb Tampa, FL Microbiology Technician III Bachelor’s degree in microbiology, Biology, or equivalent Life Science Exp: 1-2 years |
Perform routine and non-routine microbiological testing and environmental monitoring (EM) in support of sterile manufacturing operations. | 03/10/2025 |
| 1563 | Beam Therapeutics Durham, NC Manufacturing Associate / Senior Manufacturing Associate BS, MS a plus, in Life Sciences or Engineering Exp: 0-10 years |
Beam Therapeutics is looking for highly energetic Manufacturing Associates to support GMP operations in 2025 at our site in Research Triangle Park, NC. Reporting to Sr Leadership in Manufacturing, the successful candidates will provide manufacturing, operational & technical experience around commissioning, training, qualification, and routine GMP Operations. The ideal candidates will have experience in cell or gene therapy, along with demonstrated ability in a GMP environment. They will also possess the ability to successfully interface with multidisciplinary teams and build strong cross-functional relationships in a team environment. | 03/10/2025 |
| 1564 | Beckman Coulter Diagnostics Chaska, MN Scientist I Production Operations Bachelor's Degree in a Science field (preferably in Chemistry, Biochemistry, Biology) Exp: 0-2 years |
The Scientist I Production Operations for Beckman Coulter Diagnostics is responsible for following established operation procedures, maintaining appropriate training records for your role, sustaining a smooth flow of material, and the execution of work orders to on-time completion. This position is part of the Upstream Value Stream located in Chaska, MN, and will be on-site. In Upstream Value Stream, our goal is on-time delivery of cell culture, purifications, and conjugations to support on-time delivery of immunoassays to patients. You will be a part of the Upstream Value Stream focusing on Conjugations. If you thrive in a fast-paced dynamic role and want to work to build a world-class manufacturing organization—read on. | 03/10/2025 |
| 1565 | BD San Diego, CA Biochemist II - Bead Manufacturing Master’s degree in science-related field Exp: 1-3 years |
The Biochemist II, Beads Manufacturing must have working knowledge of fluorescence microparticle manufacturing. This role will conduct data analysis to solve complex problems with various factors. The Biochemist II is responsible for improving process efficiencies and product quality. This position will also support and participate in continuous improvement projects as identified by the leadership team and assigned by the Senior Manager. | 03/10/2025 |
| 1566 | BD El Paso, TX Ld Tech. QA Bachelor’s degree Exp: 1+ years |
Lead Technician in Quality Assurance assures consistent quality of production by developing and enforcing good manufacturing practice (GMP) systems and support on validation activities. | 03/10/2025 |
| 1567 | Alcami Morrisville, NC Manufacturing Technician II (Sterile Injection) Bachelor’s degree Exp: 1-2 years |
The Manufacturing Technician II (Compound/Fill/Finish) is accountable for results in a fast-paced environment and assists with the manufacturing of sterile injectable products in vial and syringe configurations for clinical/commercial distribution. The Manufacturing Tech II is a key role responsible for executing advanced production tasks involving compound, fill and finish processes for sterile injectable pharmaceutical products executed via aseptic isolator technology. This position entails a high level of technical expertise in aseptic processes requiring single-use components, ability to troubleshoot, and responsibility for maintaining quality and compliance with Good Manufacturing Practices (GMP). The Manufacturing Tech. II performs the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Tech. II employs acceptable techniques while working in manufacturing environments, including PPE gowning. The candidate must have the ability to learn specific department procedures, have a general understanding of Good Documentation Practices (GDP) and GMP, and follow directions from leadership/peers to ensure manufacturing goals are met. | 03/05/2025 |
| 1568 | Alcon Forth Worth, TX Senior Scientist - Ocular Health (Formulation Development) Master's Degree Exp: 0+ years |
We foster an inclusive culture and are looking for diverse, talented people to join Alcon and we are looking for a Senior Scientist - Ocular Health (Formulation Development) in Fort Worth, TX. The Senior Scientist will lead and contribute to the research and development of new formulations and biomaterials, focusing on novel ophthalmic materials development. This role supports the advancement of extraocular and intraocular materials. The Senior Scientist will play a key role in developing innovative solutions for topical ophthalmic products such as artificial tear and contact lens care solution. This position involves formulating and optimizing products with an emphasis on surface interaction, material-cellular interaction, structure-property relationship. The ideal candidate will have substantial experience in formulation development. | 03/05/2025 |
| 1569 | Alcon Johns Creek, GA Opto-Mechanical Engineer Master’s degree Exp: 0+ years |
The Opto-Mechanical Engineer designs, models, analyzes, and tests optical, electro-optical, and opto-mechanical systems and components, including sensors, lasers, fiber-optics, and telecommunications products. Conducts research and development into phases of physical optics and geometric optics, lasers, laser characteristics, laser maintenance, and broadband optical sources. Applies research of complex optical systems to achieve desired optical outcomes. Develops component specifications, tolerances, simulations and tests procedures for electro-optical systems and components. Uses design-to-cost models, six sigma methodology, and other methods to assure and verify optical design requirements are met. | 03/05/2025 |
| 1570 | Alcon Houston, TX Controls System Engineer Master’s degree Exp: 0+ years |
As a Control Systems Engineer supporting our manufacturing site, you will be trusted with providing engineering skills and support to help develop software and hardware control solutions and for the design, programming, installation, modification, troubleshooting, and improvement of major systems at Houston, TX. | 03/05/2025 |
| 1571 | Alcon Johns Creek, GA Associate I, Quality Control Labs Bachelors’ Degree in Scientific Discipline Exp: 1-2 years |
Conduct Quality Control testing of materials and production samples as required to support contact lens production, performing assigned tasks according to approved SOP’s, methods, and procedures with adherence to cGMP, FDA, and Corporate Quality policies and regulations. Perform routine and non-routine incoming inspection procedures in generating information for the release of materials for production use, as well as to communicate the disposition of materials to internal and external customers (with minimal supervisory or designee direction). This position also assists in the solution of technical problems, with defined scope. | 03/05/2025 |
| 1572 | Alcon Johns Creek, GA Senior Mechanical Engineer Master’s degree Exp: 0+ years |
We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As an Sr. Mechanical Engineer supporting the U.S. Development of Process and Piot Engineering Team in Duluth, GA, a typical day will include: Development, design, installation, commissioning, qualification and validation of new equipment, Communication and coordination with internal/external vendors during the implementation, commissioning, FAT and SAT, Provides expert level support and works with the various internal/external vendors/customers on key systems/deliverables, Collaborates and partners with associates from multiple disciplines, including Process Development, Research and Production, to ensure project success, Provides support, as needed, and generates required technical documentation including standard operating procedures (SOPs), training manuals and validation protocols in accordance with GMP guidelines, Identify, design and implement improvements to machines and processes related to support of contact lens development / manufacturing, Troubleshoot and correct issues related to complex production equipment used in the contact lens development / manufacturing process, Design and execute protocols for product development, and prepare documentation related to procedures, training, work instructions, validations, reports, etc., Support maintenance plans/spare part infrastructure to ensure that the required spare parts are available to reduce machine down times | 03/05/2025 |
| 1573 | Aldevron Fargo, ND Quality Control Analyst I, Environmental Monitorin Bachelor’s degree in microbiology or related scientific field Exp: 0-1 years |
This position is part of the Quality Control department located in Fargo, ND and will be an on-site position. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Quality Control Environmental Monitoring Team and report to the QC Environmental Monitoring Supervisor, and be responsible for sampling, detecting, quantifying, and identifying possible contaminants that may interfere with the quality of the product during the different stages of the manufacturing process. | 03/05/2025 |
| 1574 | Aldevron Fargo, ND Scientist I R&D MS degree in biology, molecular biology, biochemistry, chemistry, or related discipline Exp: 1+ years |
This position is part of the R&D department located in Fargo, ND and will be on-site. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Analytical Method Development unit and report to the Director, Analytical Development responsible for mRNA Analytics. | 03/05/2025 |
| 1575 | Alexion Durham, NC Sr. Associate Scientist I, Vector Production, Viral Vector Product Development Master’s degree in biology, or a relevant field Exp: 1-2 years |
This position will play a key role in Alexion’s Viral Vector Product Development, Vector Production team, interacting with internal teams within the Genomic Medicine and Product Development Clinical Supply groups. The senior associate scientist will be responsible for supporting both upstream and downstream AAV manufacturing. | 03/05/2025 |
| 1576 | AlivaMab Biologics San Diego, CA Research Associate I, Molecular Biology BS in Molecular Biology, Biomedical Engineering, or a related scientific field Exp: 0-3 years |
AlivaMab Biologics is seeking an outstanding individual to join our Antibody Engineering Team to support molecular cloning for the generation of expression constructs. As part of an interdisciplinary research team, the selected individual will be a key contributor to the progression of exciting antibody discovery and engineering efforts and contribute to technological development in the Molecular Biology group. This position will report to the Senior Scientist, Antibody Engineering, and work closely with scientists in the Protein Sciences and Antibody Discovery teams. | 03/05/2025 |
| 1577 | Alkermes Waltham, MA Healthcare Compliance Associate BS/BA Exp: 1-2 years |
The Healthcare Compliance Associate will report to the Director of Healthcare Compliance on the Compliance Monitoring and Auditing Plan. This position will require extensive domestic travel and will play an important role in fostering a culture of compliance. | 03/05/2025 |
| 1578 | Alkermes Wilmington, OH Manufacturing Process Technologist BS Degree in Engineering, Chemistry or Biology Exp: 1-2 years |
In the assigned manufacturing area, directly supports the Aristada Manufacturing Process. Actively supports ongoing manufacturing efforts in terms of quality and efficiency, provides an interface with Development and Engineering in technology transfer of new processes and process upgrades to existing technologies, and supports Corrective and Preventive Action programs. Conducts real-time monitoring/trending of manufacturing processes and finished product analytical data. | 03/05/2025 |
| 1579 | Alkermes Waltham, MA Sr. Research Associate II, Electrophysiology MS degree Exp: 1-5 years |
The Neurophysiology Group within the Research and Development organization is searching for an experienced electrophysiologist to support novel drug discovery research in CNS disorders. This position will be part of a larger multidisciplinary team challenged with interrogating the pharmacological properties and synaptic mechanism(s) of action of compounds in a variety of neuronal systems. Individuals with exceptional neurophysiology experience are encouraged to apply. The ideal candidate will have neuroscience research experience employing a variety of in vitro/in vivo electrophysiology techniques including traditional whole-cell patch-clamp, extracellular field potential recordings, and qEEG. Additional computational or programming experience is also required. Highest priority will be given to candidates with a strong desire to be in the laboratory designing and conducting experiments to support discovery projects. | 03/05/2025 |
| 1580 | ALSTEM Richmond, CA Research Associate B.S. or M.S. degree in Biochemistry, Molecular Biology or related discipline. Exp: 1 year |
ALSTEM is looking for a highly organized and energetic Research Associate with a B.S or M.S. degree to join its scientific team. The candidate will be responsible to work as a team at all levels which will include but will not be limited to product testing and QC, and custom service projects following SOPs and protocols to support customer workflows. | 03/05/2025 |
| 1581 | Altasciences Columbia, MO Laboratory Supervisor Bachelor’s degree in a scientific discipline Exp: 0-3 years |
Responsible for managing Research Associates and assisting Scientists on studies/projects. Assists with training other laboratory staff in technical procedures. Assist with evaluating and optimizing the utilization of laboratory resources to attain operational goals, meet study deadlines, and deliver quality results. Works with Laboratory Sciences Senior Manager of Operations in formulating current and long-range plans, objectives and policies. | 03/05/2025 |
| 1582 | Altasciences Everett, WA Scientist, Ligand Binding Assays MS Exp: 1 year |
The Scientist, LBA provides technical and scientific expertise in ligand binding assays for method development, validation/qualification and execution of analytical projects in support of preclinical /clinical studies. The Scientist will ensure the overall integrity/quality of assigned studies. The Scientist can also be designated as the main contact for client interactions laboratory for their assigned projects. | 03/05/2025 |
| 1583 | Altasciences Columbia, MO Scientist Bachelor’s degree in Immunology/ Biology/ Chemistry or equivalent discipline Exp: 6 months |
Are you looking for your next profession in Preclinical studies? Start your career with Altasciences while working in our new state-of-the-art laboratory! Altasciences has just completed an 8,000-square-foot expansion of our laboratory in Columbia, MO and we are looking for exceptional analysts to join our growing team. You will assist in daily activities and operation of the Laboratory Sciences department including equipment maintenance, stocking supplies and general cleaning. You will also support and perform data collection activities including ligand binding assays, and/or flow cytometry, and/or cell-based assays, and/or mass-spectrometry. We are hiring for all levels of Scientist, so apply today! | 03/05/2025 |
| 1584 | Altasciences Everett, WA Research Associate - Laboratory Sciences Bachelors degree Exp: 6 months |
Assist in daily activities and operation of the Laboratory Sciences department including equipment maintenance, stocking supplies and general cleaning. Support and perform data collection activities including LC-MS/MS, qPCR, DNA isolation, ligand binding assays, and flow cytometry, as assigned. | 03/05/2025 |
| 1585 | Lighthouse Laboratory Services Greenville, NC LCMS Laboratory Technologist B.S. in chemistry, physics, toxicology, biochemistry, biological science, clinical laboratory science, or related field. Exp: 1 year |
This is an exciting opportunity for growth within the lab industry! Lighthouse Laboratory Services is seeking a highly motivated and experienced Full Time LCMS technologist to join our laboratory in Greenville, NC. The technologist will be responsible for the day-to-day operations of the toxicology laboratory, sample prep and processing, ensuring the delivery of high-quality testing services, and daily laboratory operations. | 03/05/2025 |
| 1586 | Lighthouse Laboratory Services Dickson, TN LCMS Laboratory Technologist B.S. in chemistry, physics, toxicology, biochemistry, biological science, clinical laboratory science, or related field. Exp: 1 year |
This is an exciting opportunity for growth within the lab industry! Lighthouse Laboratory Services is seeking a highly motivated and experienced Full Time LCMS technologist to join our laboratory in Dickson, TN. The technologist will be responsible for the day-to-day operations of the toxicology laboratory, sample prep and processing, ensuring the delivery of high-quality testing services, and daily laboratory operations. | 03/05/2025 |
| 1587 | AltPep Corporation Seattle, WA Senior Research Associate Master’s degree Exp: 1+ years |
We are seeking a meticulous and dynamic Senior Research Associate to join our translational chemistry team. As part of this role, you will be responsible for conducting and supporting laboratory research, ensuring the highest standards of quality and precision. Your contributions will be critical to the success of our research and development efforts, and you will have opportunities to work both independently and collaboratively within our innovative team. | 03/05/2025 |
| 1588 | Alvogen Norwich, NY Chemist I BS in Chemistry, Biochemistry, Microbiology or Biology or related discipline Exp: 0-3 years |
Performs routine testing to assess the conformance of raw materials, finished products, and/or stability samples to predetermined product specifications. Performs routine testing in conformance with approved procedures, accurately and concisely documents data, and reports results. Demonstrates a basic knowledge of SOP’s and GMP regulations as related to the pharmaceutical quality control laboratory. | 03/05/2025 |
| 1589 | Ambry Genetics Corporation Aliso Viejo, CA Automation Technologist II BS and/or MS degree in a life sciences field: Biology, Bioengineering, Molecular Biology or related field Exp: 1+ years |
The primary duties of this position are to assist other Automation Team members in assay automation development, as well as support the Clinical Laboratory by aiding in recovery and troubleshooting validated laboratory instruments. This position also plays a role in designing, optimizing, validating, maintaining, and troubleshooting automation tools for our clinical diagnostic assays. | 03/05/2025 |
| 1590 | Amneal Piscataway, NJ Scientist, Quality Control Master Degree (MBA) Chemistry or related science discipline Exp: 1+ years |
The Scientist II - QC is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. | 03/05/2025 |
| 1591 | Amneal Branchburg Township, NJ Scientist, Quality Control Technical Services Master Degree (MBA) in Chemistry or related science discipline Exp: 1+ years |
The Scientist II - QC is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. | 03/05/2025 |
| 1592 | AstraZeneca Waltham, MA Scientist, Oncology Bioscience MS in Biology, Oncology, Biochemistry, Pharmacology, Immunology or a related field Exp: 1+ year |
Would you like to apply your expertise to impact drug development in a company that follows the science and turns ideas into life-changing medicines? Then employment at AstraZeneca might be the right choice for you! We are seeking a highly motivated Scientist in Oncology Targeted Discovery with strong scientific and technical expertise in oncology research and a track record of scientific excellence to join our team in Waltham, MA USA. As a Scientist in our Oncology R&D department, you will be a key member of a team focused on supporting oncology projects through the drug discovery and development process. You will bring your theoretical and practical expertise in cancer biology to establish assay systems and deliver datasets that will have a direct impact on targeted therapeutics. | 03/05/2025 |
| 1593 | Andelyn Biosciences Columbus, OH GMP Scientist I BS Exp: 0+ years |
The GMP Operations Scientist I is responsible for supporting all aspects of Good Manufacturing Practices (GMP) production in the Clinical Manufacturing Facility (CMF). Working in collaboration with the manager of GMP operations and staff, the scientist, I will provide hands-on assistance for all day-to-day GMP production operations, including the execution of production processes, documentation, and facility and equipment maintenance. The Scientist I will support production efforts to deliver all products in a timely, compliant, and fiscally responsible fashion by following appropriate practices, production documentation, and Standard Operating Procedures (SOPs) for manufacturing biological products. | 03/05/2025 |
| 1594 | Andelyn Biosciences Dublin, OH Scientist II Masters Exp: No exp |
A Scientist II, in Process Devlopment, will support upstream and downstream process development activities including responsibilities in bioprocessing and analytics. Working in close collaboration with PD leadership and PD scientists, scientist II will support the execution and completion of projects involving platform development, optimization, in-process characterization, and tech transfer following appropriate regulatory practices, timelines, documentation, and standard operating procedures. Prior experience in the purification of biologics is preferred. He/She will keep abreast with state-of-the-art technologies and scientific advancements in the field and participate in discussions on scale-up of processes, process qualification, and strategies for process improvement. | 03/05/2025 |
| 1595 | Andelyn Biosciences Dublin, OH Scientist I BS Exp: No exp |
The Scientist I position will support upstream and downstream process development and responsibilities in bioprocessing and analytics. The Scientist I will provide hands-on assistance for day-to-day process development production operations, including execution and development of production and purification processes, development of in-process assays for physical and functional characterization of the product, documentation, and participate in scientific discussions. | 03/05/2025 |
| 1596 | Ani Pharmaceuticals Baudette, MN Quality Control Chemist Bachelors degree in chemistry, biochemistry, microbiology or closely related field/major. Exp: 1-3 years |
The QC Chemist position is responsible for independently performing testing in a pharmaceutical Quality Control laboratory. All work will be conducted in accordance with standard operating procedures and test methods. This includes performing testing on raw material, in-process and finished product samples. Execute compendia method validations, method transfers and validation support of new product development. Set up and confirm suitable operation of equipment and instrumentation. Collect data and generate/report results in accordance with governing test methods and SOPs. | 03/05/2025 |
| 1597 | Ani Pharmaceuticals Baudette, MN QA Specialist I Bachelors degree is required. Chemistry, medical technology, microbiology Exp: 1-2 years |
This position is responsible for providing support to the Manufacturing and Packaging Operations to ensure relevant procedures are followed and meet GMP requirements. This includes, but is not limited to the following: Perform packaging line inspections/audits and provide assurance that packaging operations are compliant with applicable SOPs and cGMPs. Perform finished product attribute sample inspection and evaluation of finished products physical characteristics prior to packaging. Perform annual retain sample inspections and control finished product and raw material retain samples stored in the reserve sample room. Monitor GMP areas for compliance with general GMP requirements such as proper gowning and cleanliness, per CFR21 Subpart A General Provisions to assure they reflect current practices and meet industry standards and cGMP requirements. Perform other duties as assigned or requested. | 03/05/2025 |
| 1598 | Anika Bedford, MA QC Microbiologist I, Environmental Monitoring Bachelors Degree Exp: 1-2 years |
The QC Microbiologist I, Environmental Monitoring will learn, understand, and perform routine entry level sampling of cleanrooms and utilities according to written procedures under cGMP conditions; as well as tasks involved with clerical and logistical laboratory tasks. | 03/05/2025 |
| 1599 | Aquestive Warren, NJ Formulation Scientist MS in science Exp: 0-5 years |
A member of the R&D team responsible for the design and development of drug products for the targeted delivery of active pharmaceutical ingredients, including orally dissolving thin films for transmucosal delivery or lotions, ointments, and creams for topical delivery. | 03/05/2025 |
| 1600 | Ardena Somerset, NJ QC/EM Sampling Technician Bachelor’s Degree Exp: 1+ years |
This position is responsible for the timely sampling of incoming materials, supporting sample coordination activities and environmental monitoring of the facility and utilities at Ardena Somerset. | 03/05/2025 |
| 1601 | Ardena Somerset, NJ Senior Associate Microbiologist BS in Microbiology or related science. Exp: 1-3 years |
The Microbiology Department is responsible for performing microbial testing of raw materials and finished products (for clinical, commercial, and customer products) according to current compendia methodology. The Microbiology Department is also responsible for Environmental Monitoring of the facility and utilities at Catalent Somerset. The Senior Associate Microbiologist reports to the Microbiology Manager/Principal Microbiologist/Senior Microbiologist. This position contributes significantly to the successful timely testing and releasing of Raw Materials, in-process samples, and Finished Products of GMP and/or Commercial pharmaceutical Manufacturing. The primary responsibilities of this position will be performing microbial activities in support of the manufacturing of pharmaceutical products under the supervision of other microbiologists. These activities include raw material testing, in process testing, finished product testing, environmental sampling and testing, and water sampling and testing. | 03/05/2025 |
| 1602 | ARL Bio Pharma Oklahoma City, OK Chemist I - Analytical Bachelor’s degree in chemistry or related science Exp: 1-2 years |
Join a company where you can make a difference from day one and help make the world a better and safer place. ARL Bio Pharma provides analytical and microbiological testing for the pharmaceutical industry. Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug manufacturers, and raw material suppliers bringing excellence to pharmaceutical sciences and making pharmaceuticals safer. This position is a fantastic stepping-stone for those with some basic experience looking to expand their career in the interesting world of the pharmaceutical industry. The Chemist I is responsible for utilizing established methods and standard lab equipment/instrumentation (HPLC, IC) to qualitatively and quantitatively analyze routine pharmaceutical substances and formulations. | 03/05/2025 |
| 1603 | ARL Bio Pharma Oklahoma City, OK Chemist I - Chemistry Bachelor’s degree in chemistry or related science Exp: 0-2 years |
This position assists in maintaining the cleanliness of the laboratory, the organization of supplies, reagents and standards. Additionally, this position provides a backup for the daily calibration and/or verification of the balances and pH meter when the Lab Technician is unavailable. The employee will have basic knowledge of commonly used laboratory concepts, practices, procedures and instrumentation and will perform tests commensurate with skill level with some supervision. | 03/05/2025 |
| 1604 | ARL Bio Pharma Oklahoma City, OK Microbiologist I Bachelor’s degree in Microbiology or related science Exp: 0-2 years |
Under the supervision of the laboratory supervisor the Microbiologist I provides a high level of quality pharmaceutical microbiology testing as well as effective customer service to ARL Bio Pharma clients. This is a safety sensitive position as defined by state and federal laws that will require working with hazardous materials and/or handling medicine. | 03/05/2025 |
| 1605 | Arraystar Rockville, MD Lab Assistant - Molecular Biology Bachelor’s degree in a relevant biological field Exp: 1-2 years |
Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. Assist with the generation and updating of laboratory SOPs. Perform basic lab maintenance tasks such as ordering lab supplies, and keeping detailed lab records. Communicate with clients to obtain/verify information of their projects, orders or requests. | 03/05/2025 |
| 1606 | Arrowhead Pharmaceuticals Madison, WI Associate Scientist I, Discovery Chemistry Operations B.S. Chemistry or Biochemistry degree Exp: 0-2 years |
Arrowhead Pharmaceuticals is seeking an Associate Scientist to join the Discovery Chemistry Department. The successful candidate will primarily focus on oligonucleotide synthesis, conjugation, purification, and characterization. They will be joining a team of highly motivated and experienced scientists and will contribute to the success of Arrowhead programs. | 03/05/2025 |
| 1607 | AbbVie Irvine, CA In Vitro Associate Scientist II MS Exp: No exp |
The In Vitro Associate Scientist II, as part of Local Delivery Translational Sciences (LDTS) at the Irvine, California site at AbbVie is responsible for developing and applying novel physiologically relevant in vitro models to characterize drug, biologic, formulation and sustained delivery formulation (e.g. sustained release implants) performance, erosion, and safety/tolerability. The In Vitro Associate Scientist II serves as a subject matter expert collaborating with colleagues in Clinical Pharmacokinetics, Pre-Clinical Safety, and other research functions to design in vitro experiments and develop novel in vitro models to address needs of AbbVie projects, specifically for botulinum toxin, eye care and aesthetics therapeutic areas. As a member of a small team, this individual will independently develop and perform in vitro and related bioanalysis studies, document experiments, prepare formal reports, and present findings to key stakeholders, This individual should be a self-starter who is eager to learn and thrives in a collaborative, fast-paced environment, with a desire to make an impact by interacting closely with scientists from other disciplines and functional areas. | 02/24/2025 |
| 1608 | AbbVie Irvine, CA Associate Scientist II - In Vivo Pharmacology Master’s Degree Exp: No exp |
The Neurotoxin Research Group at AbbVie is seeking a highly motivated and innovative candidate for the role of Associate Scientist II, In vivo pharmacology. The successful candidate for this position will contribute to projects aimed at the pharmacological characterization of protein-based therapeutics. Under supervision by senior personnel, he/she will be required to work on a variety of in vivo animal pharmacology models to help characterize and evaluate biological compounds. This individual will need to organize, analyze, interpret, and present results to senior personnel or in team meetings. A good understanding of animal models, neurology, and pharmacology is required. Experience in handling and injecting rodents by different routes is required. Working knowledge of neuroscience and in vivo motor pharmacology is an advantage. The successful candidate will be collaborating extensively with other Research Associates and Scientists, while taking personal responsibility for the success of assigned tasks and projects. | 02/24/2025 |
| 1609 | AbbVie Worcester, MA Associate Scientist II/ Scientist I, Gastro Pharmacology Master’s Degree Exp: No exp |
We are looking for a highly motivated scientist to join our Gastroenterology Disease Area Team in Discovery Research Immunology located in Worcester, MA. The ideal candidate should be independently driven, highly collaborative, and results oriented. They will support in vitro and in vivo research efforts for our existing early-stage through late-stage discovery portfolio programs. Responsibilities include conducting, analyzing, and reporting on in vitro and in vivo assays to explore key biological questions related to IBD diseases, such as ulcerative colitis and Crohn’s disease. The candidate should be proficient in basic laboratory techniques such as pipetting, cell culture, flow cytometry, qPCR, and ELISA. The ideal candidate should also have hands-on experience with in vivo PK/PD rodent studies as well as substantial experience culturing and designing functional assays with primary human cells (e.g. proliferation, differentiation, co-culture). | 02/24/2025 |
| 1610 | Abeona Therapeutics Cleveland, OH Analyst Quality Control Micro Analytical BS in biochemistry, biology, microbiology, molecular biology or other relevant discipline Exp: 1-3 years |
The Quality Control Analyst I performs routine laboratory activities in support of Good Manufacturing Practices (GMP) testing for Quality Control (QC). Performs in-process and release testing for drug substance and drug product. Interacts with employees internal and external to Quality Control. | 02/24/2025 |
| 1611 | Abeona Therapeutics Cleveland, OH Associate, Manufacturing - Operations MS in scientific discipline Exp: 1-2 years |
Abeona is looking for a Manufacturing Operations Associate to join our team in Cleveland, OH. The successful candidate will be responsible for Manufacturing initiatives supporting multiple product pipelines. The candidate will be an integral part of a fast-paced group responsible for the manufacture of retroviral vector and autologous gene-corrected cell therapies. Responsibilities will include executing protocols and manufacturing clinical and commercial material across multiple products as well as supporting process optimization work and document generation. The ideal candidate will have experience in production of biologics in a controlled cGXP setting. Strong aseptic and cell culture technique as well as collaborative work in a team is an integral part of this position. | 02/24/2025 |
| 1612 | Abeona Therapeutics Cleveland, OH Document Control/Archivist Specialist I, Quality Assurance Bachelor’s degree in related field Exp: 1-3 years |
The Specialist I, Quality Assurance performs routine activities associated with manufacturing of cell and gene therapy products at the Abeona Therapeutics Inc. site in Cleveland, OH. This position is responsible for document review which includes, but is not limited to: editing, formatting, and proofreading prior to SME approval in the Quality Management System. This position is also responsible for document archival and retention post product disposition. The Specialist I, Quality Assurance will report to the Supervisor, Quality Assurance or above and will support all document review and retention/archiving for the site. | 02/24/2025 |
| 1613 | Abeona Therapeutics Cleveland, OH Quality Control Analyst I (QC Analytical) BS in biochemistry, biology, microbiology, molecular biology or other relevant discipline Exp: 1-3 years |
The Quality Control Analyst I performs routine laboratory activities in support of Good Manufacturing Practices (GMP) testing for Quality Control (QC). Testing includes qPCR, immunostaining, protein characterization and product specific analytical test methods. Interacts with employees internal and external to Quality Control. | 02/24/2025 |
| 1614 | Abeona Therapeutics Cleveland, OH Specialist I, Quality Assurance Bachelor’s degree in related field Exp: 1 year |
The Specialist I, Quality Assurance performs routine activities associated with manufacturing of cell and gene therapy products at the Abeona Therapeutics Inc. site in Cleveland, OH. This position supports the maintenance of the quality systems in support of a cGMP Operations, corrective and preventative actions, quality events management (e.g., nonconformances, deviations, etc.), training, document management and ensuring procedural and regulatory compliance throughout the manufacturing process. The Specialist I, Quality Assurance will report to the Supervisor, Quality Assurance or above. | 02/24/2025 |
| 1615 | Adare Pharma Solutions Vandalia, OH Analytical Scientist I or II Master’s Degree in Chemistry or related discipline Exp: 0-1 years |
The Analytical Scientist I or II will support the development and validation of analytical methods for raw materials, work-in-process, and finished products to provide testing support for the formulation development and clinical supplies release process. The Scientist II will also be expected to provide some training, coaching, and mentoring for more junior scientists. | 02/24/2025 |
| 1616 | Adesis New Castle, DE Research Chemist Bachelor of Science Exp: 1-2 years |
Responsible for assisting chemists in performing various purifications of target compounds using various methods, including, but not limited to preparative high performance liquid chromatography (prep HPLC), normal phase and reverse phase chromatography, and recrystallization. | 02/24/2025 |
| 1617 | ADMA Biologics Boca Raton, FL Laboratory Technician - Automation Bachelor’s degree in related science discipline Exp: 0-2 years |
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We have an exciting opportunity available for a Laboratory Technician - Automation in Boca Raton, FL! The Laboratory Technician - Automation performs automated laboratory testing to support hyperimmune products for ADMA Biologics. This position is responsible for the receipt, testing and on-time delivery of donor testing and maintaining a cGMP compliant laboratory. Maintaining communication with group leader or department manager to support cross-function relationships with plasma centers and ADMA plasma operations. | 02/24/2025 |
| 1618 | ADMA Biologics Boca Raton, FL Scientist II Process Development Master’s degree in biochemistry, chemical engineering, biophysics, biology, or a related field. Exp: 0-5 years |
We are excited to offer a new opportunity for a Scientist II, Process Development based in Boca Raton, FL! In this role, the Scientist II, Process Development will contribute to the advancement of protein purification processes, playing a key part in our development efforts. | 02/24/2025 |
| 1619 | Admera Health South Plainfield, NJ Associate Scientist I/II (Lab) Bachelor’s degree or MS in Biological Sciences Exp: 1-3 years |
Preparing solutions and reagents for performing assays on the bench. Perform Next Generation Sequencing-based genomic assays on different workflows (few listed below): o RNAseq. Whole Genome Sequencing. Whole Exome Sequencing. Carry out genomic assays under Biosafety Level II Policies and in regulatory compliance. Perform Operational Qualification and Performance Qualification on Next Generation Sequencers. Strictly follow standard operating procedures set forth for processing biological specimens while complying with laboratory safety protocols. Strict recordkeeping of all laboratory procedures. Continue acquiring next generation sequencing knowledge to support molecular biology techniques. Collaborate within the group and cross departmental to achieve goals. | 02/24/2025 |
| 1620 | ABS Livermore, CA Operations Engineer B.Eng in Mechanical Engineering, Industrial Engineering, Manufacturing, or related discipline. Exp: 1-3 years |
Reporting to the Director, Engineering & Operations, the Operations Engineer will have responsibility for key aspects of ABS’ product manufacturing and operational processes. Assuming the dual roles of that of a Manufacturing Engineer and Facilities Engineer, the Operations Engineer will work on simple-to complex, high visibility/value projects with a focus on supporting production. The Operations Engineer will also support the Facilities function in a multitude of ways – compliance, procedure development, equipment maintenance, organization and much more. | 02/24/2025 |
| 1621 | Advanced Instruments Norwood, MA Mechanical Engineer I Bachelor’s degree in mechanical engineering. Exp: 1-3 years |
As a Mechanical Engineer I you will work on new product development and/or sustaining engineering tasks, prepare electro-mechanical designs, drawings, specifications for new and sustaining product lines, and provide technical guidance and expertise to projects within the R&D department as well as Manufacturing Engineers and production personnel. The Mechanical Engineer I will report to the Mechanical Engineering Manager as an individual contributor and must be capable of working with senior level engineers. You will complete detailed specifications, designs, calculations, analyses and simulations for major hardware components of a project. In this role, you will be capable of working on assembly of models and prototypes in engineering lab environment and set up and conduct non-standard or product-specific evaluation tests of prototypes. You will record observations and data, analyzes and interprets results and prepares summary reports. | 02/24/2025 |
| 1622 | New Age Industries Southampton, PA Project Engineer B.S. in Engineering (Mechanical, Chemical, Materials Science, Biomedical preferred). Exp: 0-3 years |
The Project Engineer utilizes his or her technical, project management, and problem-solving skills to organize group efforts and execute tasks towards company goals in areas such as new product development, supply chain/change management, manufacturing, and continuous improvement efforts. The Project Engineer must use software tools to create and maintain measurable progress metrics that can be communicated regularly to stakeholders. | 02/24/2025 |
| 1623 | B. Braun Medical Inc. Daytona Beach, FL QC Lab Tech II-Microbiology Bachelor's degree Exp: 1-2 years |
Performs a variety of quality control tests on products at various stages of the production process to ensure compliance with quality and reliability standards. Records statistical data. Analyzes data and writes summaries to validate or show deviations from existing standards. Recommends modifications to existing or suggests new, standards, methods and procedures. | 02/24/2025 |
| 1624 | B. Braun Medical Inc. Irvine, CA QC Chemistry Associate II Bachelor's degree in a Science related field Exp: 1-2 years |
Perform routine laboratory analysis of In-Process, finished product, raw material, stability samples and environmental monitoring according to established specifications and procedures using wet chemistry techniques or various laboratory apparatus and instruments (e.g. HPLC, UV/Visible Spectrophotometer, FTIR, TOC, pH meter etc.) in compliance with B. Braun, cGMP, GLPs, SOPs, USP and FDA guidelines. | 02/24/2025 |
| 1625 | Affinia Therapeutics Waltham, MA Research Associate, Preclinical Analytics Master's Degree Exp: 1-4 years |
Affinia Therapeutics is seeking an experienced Research Associate (job level will commensurate with experience) to join our Preclinical Analytics laboratory team. You will be part of a group dedicated to the advancing of gene therapies based on vectors derived from our unique AAV platform. You will actively contribute to the development and execution of analytical assays supporting studies conducted by the translational science team at Affinia. You will work to establish methods and analyze samples to meet timelines for our internal development programs. You will contribute to the evaluation of new analytical technologies, the development of more efficient laboratory workflows as well as maintaining a culture of quality and excellence. | 02/24/2025 |
| 1626 | AGC Biologics Bothell, WA Quality Control Associate I, Sample Management BS/BA degree Exp: 0-2 years |
Performs basic QC analysis and documents activities according to SOPs following good manufacturing processes (GMP) and demonstrates ability to learn QC methods, procedures and systems. | 02/24/2025 |
| 1627 | AGC Biologics Boulder, CO MSAT Engineer I/II BS in Chemical engineering / Biochemical engineering / Biology or other science related discipline Exp: 1 year |
We have an opportunity for an MSAT Engineer I/II to join the Manufacturing Science and Technology (MSAT) team at AGC Biologics in Boulder, CO. This position requires technical problem-solving and inter-departmental collaboration. Responsibilities will be varied, requiring time management skills and ability to deliver against fluid timelines. This role is responsible for 24/7 production support when manufacturing operations are in progress including direct Person in Plant and customer support. Other responsibilities include technology transfer support, new proposal support, quality systems support and data collection, trending, and analysis support. | 02/24/2025 |
| 1628 | AGC Biologics Boulder, CO Quality Control Associate I, Sample Management BA in Biology, Microbiology, or other scientific discipline. Exp: 0-2 years |
The Quality Control Associate I - Microbiology will focus on performing microbial and environmental monitoring assays, facility qualification, and testing of purified water and cleaning samples. This position may also review data, execute validation studies, and support commissioning of laboratory instruments. The ideal candidate will be highly motivated, organized, and have the ability to work independently. Experience in a GMP Microbiology laboratory is preferred. | 02/24/2025 |
| 1629 | AGC Biologics Bothell, WA Manufacturing Support Technician I BS/BA degree Exp: No exp |
As the Night Shift GMP Cleaning and Sanitization Technician, you will be responsible for maintaining the cleanliness and compliance of GMP regulated areas and ensuring facilities are properly restocked. You will also be expected to follow and document all sanitization processes in line with our SOPs and regulatory requirements. | 02/24/2025 |
| 1630 | AGC Biologics Bothell, WA Upstream Manufacturing Associate I/II BS/BA degree Exp: 0-2 years |
The role of the Manufacturing Associate is to act as a controller, providing essential duties to support the respective production suite, Supervisor, and Manager. On a daily basis, the Manufacturing Associate is expected to have a full understanding of the schedule and required tasks; promoting adequate assessment and response of any production demands. | 02/24/2025 |
| 1631 | AGC Biologics Bothell, WA Downstream Manufacturing Associate I/II BS/BA degree Exp: 0-2 years |
The role of the Manufacturing Associate is to act as a controller, providing essential duties to support the respective production suite, Supervisor, and Manager. On a daily basis, the Manufacturing Associate is expected to have a full understanding of the schedule and required tasks; promoting adequate assessment and response of any production demands. | 02/24/2025 |
| 1632 | Agilent Boulder, CO Manufacturing Associate - Representative Bachelor’s or Master’s Degree Exp: 1+ years |
As a Manufacturing Associate, you will check and schedule resources to ensure timely delivery. Your scientific knowledge and background will be leveraged through your review of formulation documents and active ingredient dilution to ensure that products are manufactured to specification. You will have an opportunity to become skilled in the use of a wide range of lab instruments, including but not limited to spectrophotometers, conductivity meters and auto-pipettors, all of which are essential to meeting our customers' requirements. Having the ability to learn quickly on the job, anticipate and resolve potential manufacturing and delivery issues and maintaining the highest level of quality are essential. Additionally, you will work on problems of diverse scope in which analysis of data requires evaluation of identifiable factors. You will also exercise judgment within generally defined practices and policies in selecting methods and techniques for acquiring solutions. | 02/24/2025 |
| 1633 | Agilent Carpinteria, CA Research Associate, Entry Bachelor’s Degree or Higher, or equivalent in a scientific discipline. Exp: No exp |
We are looking for a talented and dedicated Research Associate to join the CDx Group in our R&D Department. You will provide technical support to develop accurate, robust and precise assays. Your challenge will be to create value for Agilent through innovative ideas that either create new businesses or enhance existing ones. | 02/24/2025 |
| 1634 | Agilent Newport, DE Production Chemist – Particle Engineering Bachelors or Masters Degree in Chemistry, Material Science or equivalent Exp: 1+ years |
Agilent Technologies is seeking a Production Chemist for its manufacturing facility in Newport, Delaware. The Newport site is part of Agilent’s growing Consumables and Supplies Division (CSD), with a focus on liquid chromatography products. Agilent’s product quality and technological innovation lead the market. As a leader, we are entering new phases of product transformation with increased emphasis on new product and process innovation, process standardization and production efficiency. | 02/24/2025 |
| 1635 | Agilent Cedar Creek, TX Manufacturing Scientist - Genomic Reagents Testing Bachelor's degree or equivalent experience in Biological Science or a related field with chemistry, molecular biology, or biochemistry expertise. Exp: 1 year |
Join our innovative team at Agilent Technologies as a Manufacturing Scientist specializing in genomic reagents. You'll contribute to ground breaking products that advance Next Generation Sequencing (NGS), Microarray testing, and PCR-based technologies. If you're passionate about driving scientific advancements and thrive in a dynamic, collaborative environment, this role offers an exciting opportunity to grow and make a tangible impact. | 02/24/2025 |
| 1636 | Agilent Frederick, CO Manufacturing Associate Bachelor’s or Master’s Degree Exp: 1+ years |
As a Manufacturing Associate (Representative), you will check and schedule resources to ensure on-time delivery. Your scientific knowledge and background will be leveraged through your review of formulation documents and active ingredient dilution to ensure that products are manufactured to specification. You will have an opportunity to become skilled in the use of a wide range of lab instruments, including but not limited to spectrophotometers, conductivity meters and auto-pipettors, all of which are essential to meeting our customers' requirements. Having the ability to learn quickly on the job, anticipate and resolve potential manufacturing and delivery issues and maintaining the highest level of quality are critical. Additionally, you will work on problems of diverse scope in which analysis of data requires evaluation of identifiable factors. You will also exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. | 02/24/2025 |
| 1637 | Agilent Cedar Creek, TX Manufacturing Scientist - NGS Probe BS/BA in Biological Science or related field with experience in chemistry, molecular biology, and/or biochemistry. Exp: 1+ years |
Join our Next Generation Sequencing (NGS) Probe manufacturing team as a Manufacturing Scientist at Agilent Technologies. At Agilent Technologies, we are dedicated to advancing scientific discoveries that improve the quality of life. Our Manufacturing group is a collaborative and diverse team made up of members who learn quickly on the job and anticipate/resolve potential manufacturing issues while maintaining the highest level of quality. This is essential in delivering innovative, high-quality products to our customers worldwide. | 02/24/2025 |
| 1638 | Agilent Boulder, CO Manufacturing Chemist Bachelor's degree in chemistry, biology, engineering or related life science field Exp: 1+ years |
The Manufacturing Chemist position performs a wide variety of technical duties to support small scale manufacturing operations. | 02/24/2025 |
| 1639 | Ajinomoto Bio-Pharma San Diego, CA Drug Product Manufacturing Associate I Bachelors in a science or engineering discipline Exp: 0-2 years |
We are currently seeking a Drug Product Manufacturing Associate I who is responsible for executing GMP production of injectable pharmaceuticals by following all applicable SOP's. Manufacturing associates are responsible for preparing equipment and materials for GMP aseptic production and operating equipment such from glasswashers, autoclaves, depyrogenation ovens and automated filling machines. | 02/24/2025 |
| 1640 | Ajinomoto Bio-Pharma San Diego, CA QA Associate I Bachelor’s degree in a Life Sciences discipline Exp: 0-2 years |
We are currently seeking QA Associate I who is responsible for performing a wide variety of routine and semi-routine activities pertaining to assuring compliance with Quality Assurance (QA) requirements and applicable regulatory requirements. The Associate I promotes a cGMP environment and collaborates with internal team members to ensure adherence to specifications, processes, and procedures. The Associate I performs documentation review and ensures completeness and accuracy of information contained in all documents, document files, databases, and documentation systems. Understanding and execution of basic cGMP and GDP principles is required. | 02/24/2025 |
| 1641 | Akoya Biosciences Marlborough, MA Research Associate II, Histology BS Degrees in Life Sciences preferred Exp: 1-2 years |
Akoya is seeking a Research Associate II (RA-II) to work within our Akoya Advanced Biopharma Solutions (ABS) CLIA laboratory located in Marlborough, MA. This position is a full-time onsite role. The candidate will have worked in a clinical or preclinical pathology laboratory with experience in high-throughput histology with focus on immunohistochemistry. The candidate will work with lab personnel on histology processes such as grossing, processing, embedding, and microtomy. Knowledge of antibody validation methods, immunofluorescence (IF) and quantitative pathology approaches are a plus but not required. The successful candidate must have significant experience in microtomy, preferably with rotary microtomes. They should also be familiar with LIMS systems and have experience working in a regulated laboratory setting such as CAP/CLIA and GCLP. | 02/24/2025 |
| 1642 | Akron Biotech Sarasota, FL Associate, Manufacturing - Operations BA/BS in Biology, Chemistry, Bioengineering or a related field Exp: 1-2 years |
Akron Biotech is continuing to transform and further its rapidly growing capabilities and is now seeking highly motivated professionals to join our expanding team. This is an exciting opportunity to play a critical role within our organization that is driving advanced therapy development and commercialization with high quality industrial scale solutions. We manufacture and distribute components and raw materials for cell therapy discovery, development, and commercialization to meet industry needs worldwide. We offer an array of highly competitive benefits and perks to our valued associates. | 02/24/2025 |
| 1643 | Akston Biosciences Beverly, MA Research Associate I/II Bachelor’s degree in Engineering, Biology, Molecular Biology, Pharmaceutical Sciences or related field Exp: 0-3 years |
Akston is looking for a highly motivated and energetic Research Associate I/II to join our dynamic and diverse R&D team. In this role, you'll play a key part in supporting our efforts to develop innovative biologic therapies. The ideal candidate will collaborate closely with cross-functional teams, translating strategic goals into actionable plans. Experience with biological entities (e.g., fusion proteins and monoclonal antibodies) is essential. A background in analytical chemistry, biochemistry, biotechnology, chemical biology, chemical engineering, molecular biology or related fields is highly desirable. | 02/24/2025 |
| 1644 | Alcami Morrisville, NC Environmental Monitoring Technician I - 2nd Shift BS Exp: 0+ years |
The Environmental Monitoring Technician I is accountable for driving results in fast-paced environment by performing monitoring of the pharmaceutical manufacturing environment and utilities in compliance with cGMP and internal SOPs. The Environmental Monitoring Technician must be detail-oriented and possess organizational skills with a large quantity of data. | 02/24/2025 |
| 1645 | Alcami Morrisville, NC Environmental Monitoring Technician I - 1st Shift BS Exp: 0+ years |
The Environmental Monitoring Technician I is accountable for driving results in fast-paced environment by performing monitoring of the pharmaceutical manufacturing environment and utilities in compliance with cGMP and internal SOPs. The Environmental Monitoring Technician must be detail-oriented and possess organizational skills with a large quantity of data. | 02/24/2025 |
| 1646 | Alcami Morrisville, NC Scientist II - Compendial Testing, Raw Material Master’s degree Exp: 0+ years |
The Scientist II / III is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Scientist II / III may also be required to work on method development/method validation projects. For this position, HPLC, dissolution and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company). | 02/24/2025 |
| 1647 | TScan Therapeutics Waltham, MA Clinical Trial Associate BS in scientific or healthcare discipline Exp: 1-3 years |
TScan Therapeutics is a clinical-stage biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for a Clinical Trial Associate to join our Clinical Operations team to support the execution of our Phase 1 basket study in solids. The ideal candidate should have experience in supporting the execution of oncology clinical studies as well as a working knowledge of ICH GCP regulations. The candidate should a enjoy fast-paced, collaborative, and vibrant startup culture. A team player with a sense of urgency will thrive in this role. | 02/17/2025 |
| 1648 | Ultima Genomics Fremont, CA Product Engineer I BS or MS in Computer Science, Engineering, Biomedical, Electrical, Mechanical, Systems Engineering disciplines or core scientific degree Exp: 1 year |
Our Product Engineer plays a strategically important role in ensuring the company’s business success. The primary responsibilities include, but are not limited to, supporting Field Service Engineers (FSEs) and Field Application Scientists (FASs) groups with technical support, authoring and reviewing Best Known Practices (BKPs) for field deployment, and coordinating the rollout and implementation of Engineering Change Orders (ECOs) in the field. In this Product Engineer (PE) position, you will train FSE’s on best practices and be the point of contact for field escalations. PEs are system experts and sometimes work side by side with R&D to gain a deep understanding of the system. PEs will help define problem statements, develop mitigations, and are a key contributor to Corrective Action Preventative Action (CAPA) plans. | 02/17/2025 |
| 1649 | United Therapeutics Research Triangle Park, NC Bioprocess Technician - Tissue Engineering Development Bachelor’s Degree in life science, engineering, or biomedical science Exp: 1+ years |
If you're passionate about advancing research for the treatment of pulmonary hypertension and other lung diseases, this role is for you! As part of our innovative research team, you’ll play a pivotal role in developing regenerative medicine products by operating lung recellularization systems and supporting tissue engineering processes. You’ll assist in preparing human and non-human tissues, performing assays, maintaining bioreactors, and analyzing data—contributing directly to the development of groundbreaking treatments. If you thrive in a collaborative, hands-on lab environment and are eager to apply your technical skills to real-world medical solutions, this position offers a unique opportunity to make a meaningful impact. | 02/17/2025 |
| 1650 | United Therapeutics Research Triangle Park, NC Assembly Technician I Bachelor’s Degree Exp: 1+ years |
As a key member of our R&D team, you will contribute to the preparation and assembly of medical and laboratory device components, playing a crucial role in the advancement of our projects. You’ll work hands-on in the lab to assemble tubing sets, prepare cell culture media, ensure sterilization, and maintain an organized and safe environment, all while following detailed instructions to support the development of next-generation medical devices and technologies. | 02/17/2025 |
| 1651 | Unither Rochester, NY Validation Technician BS Exp: 0 years |
Assists validation efforts in many ways including the following: executes/supports equipment, cleaning, and process qualifications, takes and delivers samples, collects and compiles data for validation reports, assists in maintaining of the Validation Document Library, maintains test equipment and documentation system. | 02/17/2025 |
| 1652 | Vala Sciences San Diego, CA Research Associate (RA)/Senior Research Associate (SRA) – iPSC Manufacturing B.S. or M.S. in Cell/Molecular Biology, Biochemistry, Neuroscience, or related field Exp: 1-2 years |
We’re seeking an RA or SRA to join our dynamic induced pluripotent stem cell (iPSC) research and manufacturing program. The successful candidate will manage iPSC lines and their differentiation to different cell types, like cardiomyocytes, microglia, neurons, and astrocytes. These differentiated iPSC lines will be used for internal R&D projects, commercial research contracts, and manufacture for sale. You will evaluate and validate differentiated cell lines with biomarker detection methods like ICC or flow cytometry, and investigate and characterize cellular function using Vala’s live-cell fluorescent imaging technology. You will work in a close-knit, fast-paced team environment and adapt readily to changing needs as projects and technologies evolve. | 02/17/2025 |
| 1653 | Vantage MedTech Lenexa, KS NPI Engineer BS or MS degree in Engineering, preferably Mechanical or Manufacturing Engineering. Exp: 1-3 years |
The NPI (New Product Introduction) Engineer will be responsible for ensuring that our innovative designs are transitioned into effective and sustainable production. Our life saving products are manufactured in Kansas City and require predictable delivery of high quality, cost-effective production over 5+ year product lifetimes. You will collaborate with Vantage MedTech’s Engineering and Manufacturing teams to provide input on the device design’s manufacturability, and plan and execute the transfer of these new products to our manufacturing facility. You will be responsible for ensuring that robust manufacturing processes are created, updated and in compliance with company standards, ISO, and GMP as required. In addition, you will help drive improvement projects that impact quality and productivity. | 02/17/2025 |
| 1654 | Vaxcyte San Carlos, CA Associate Scientist I, Formulation Development BS in Pharmaceutical Sciences, Organic/ Biochemistry, Chemical / Biochemical Engineering, Biology, Chemistry or a related discipline Exp: 0-2 years |
Vaxcyte is looking for an energetic and talented individual to play a key supporting role in the Formulation Development function. Vaxcyte is focused on the development of protein conjugate vaccines. They would support manufacture of drug products to support analytical and process development groups within the Drug Product Team. In addition, they would also support scientists in the execution of large and complex experimentation as well as routine studies and testing. | 02/17/2025 |
| 1655 | Vedanta Biosciences Cambridge, MA Contract - Research Associate, Analytical Development BS in a life science Exp: 1+ years |
Vedanta is seeking a research associate to join the Analytical Development Group, supporting the molecular biology team within Analytical Development. We are looking for an individual who is curious, intrinsically motivated, excited to collaborate, and an excellent communicator. | 02/17/2025 |
| 1656 | Veloxity Labs Peoria, IL Associate Scientist II Bachelor’s degree in science (chemistry/biochemistry preferred) Exp: 1-2 years |
As an Associate Scientist II, you will be using state-of-the art technologies to perform bioanalytical testing for emerging pharmaceutical and biopharma companies. At Veloxity, we hire driven and motivated individuals and provide training and career advancement opportunities within our organization. | 02/17/2025 |
| 1657 | Veracyte Austin, TX Specimen Processor Bachelor’s degree Exp: 0-2 years |
The Specimen Processor in this CLIA Laboratory is a critical member of the laboratory team, responsible for receiving, accessioning, and documenting specimens with precision. This role requires accurate data entry, proactive identification, and resolution of sample integrity issues. Flexibility in scheduling, including holidays and variable shifts, is essential to meet operational demands. | 02/17/2025 |
| 1658 | Vericel Cambridge, MA Associate I, Cell Therapy Manufacturing Bachelor’s degree (Life Sciences or related field) Exp: 0-2 years |
Responsible for the execution of process steps to manufacture commercial cell therapy products meeting internal and regulatory requirements. | 02/17/2025 |
| 1659 | Vericel Cambridge, MA Quality Control Analyst, II Master’s Degree Exp: 0+ years |
Responsible for performing routine and complex testing of in-process samples and final products in accordance with SOPs for product release and validation. | 02/17/2025 |
| 1660 | Vericel Cambridge, MA Engineer, I Bachelor's degree in Chemical or Mechanical Engineering or a related engineering field. Exp: 0-2 years |
The Engineering department is primarily responsible for the detailed design, startup, troubleshooting, commissioning, optimization and lifecycle support of manufacturing equipment, facilities, and utility systems. | 02/17/2025 |
| 1661 | Versatope Therapeutics Lowell, MA Process Development Scientist Masters degree in biotechnology Exp: 0-5 years |
At Versatope Therapeutics you will work alongside other bright, motivated scientists in developing groundbreaking vaccines and therapeutics. We hire amazing people who are intensely curious and continually questioning. | 02/17/2025 |
| 1662 | Vigil Neuroscience Watertown, MA Scientist, Discovery Biology (Contract) M.S. Exp: 1+ years |
Vigil is looking for a skilled and motivated Scientist to join our team. The successful candidate will be responsible for execution of assays for novel therapeutics targeting neuroinflammation and neurodegeneration, with a primary focus on microglia. The ideal candidate is highly organized, independent, and collaborative. | 02/17/2025 |
| 1663 | Vivex Miami, FL Staff Quality Assurance Engineer Bachelor’s degree in engineering or a related technical discipline (e.g. Biology, Chemistry, etc.) Exp: 1 year |
The Quality Assurance Engineer develops, applies, revises, and maintains quality metrics to support areas of operations at Vivex Biologics, Inc. The role assists in the planning, development, implementation, communication, and maintenance of Vivex’s quality management systems, polices, documentation, data, and customer requirements. The Quality Assurance Engineer is expected to work with all departments to ensure compliance, that the final products are safe, reliable, and effective, and the successful and timely completion of projects. The Quality Assurance Engineer is mainly responsible for the maintenance of CAPA system items. They play a key role in preventing issues or fixing them if they arise by defining, monitoring, and approving the processes needed to achieve production standards. | 02/17/2025 |
| 1664 | Vivex Miami, FL Operations Processing Technician I Bachelor’s Degree in science or related Exp: 0-1 years |
The Operations Processing Technician I support the processing and documentation requirements of tissue during the cleaning, cutting, shaping, inspecting, and packaging operations for transplantation purposes. The Operations Processing Technician I is also responsible for ensuring that all equipment and supplies used for processing are maintained and ready for use, and that all Processing Room maintenance is completed daily while complying with Quality Assurance requirements as mandated by federal, state, and trade regulations. | 02/17/2025 |
| 1665 | Vivex Miami, FL IC/QC & Distribution Coordinator I Bachelors Exp: 0-1 years |
The IC/QC & Distribution Coordinator I - Weekend Shift is responsible for maintaining a high level of inventory accuracy and integrity within the Tissue Bank. Ensure that Inventory Control Operations are in Compliance with the State and Federal Regulations and AATB Standards. Promotes Lean Behaviors across the organization (This includes Participating in Try storming, Brainstorming and Lean Related Initiatives). Resourceful in completing deadlines and can multitask effectively. | 02/17/2025 |
| 1666 | West Williamsport, PA Tooling Engineer Bachelor’s Degree in a technical discipline to include: mechanical engineering, manufacturing engineering, industrial, or plastics. Exp: 1-3 years |
The Tooling Engineers objective is to support the facility, commercial team, and mold tooling vendors on new mold development projects and legacy mold improvement projects. In parallel, the position also provides innovative solutions and services to the tooling group and other departments within the company, where possible, to assist with meeting company goals and objectives. In this role, you will be part of a team that relies on effective teamwork and global collaboration in a fast pace and dynamic environment. This role may be responsible to set-up, operate, and monitor CNC and/or manual Milling machines to provide operational support for the construction, assembly, and/or repair of molds, dies, and ancillary equipment. | 02/17/2025 |
| 1667 | West Exton, PA Associate Scientist Bachelor's Degree in Biology, Chemistry or a relevant scientific field preferred Exp: 0-3 years |
In this role, you will be responsible for performing testing of products for internal and external customers using a variety of analytical techniques in a QC/cGMP environment. You may be assisting in updating procedures for instrumentation, test instructions, and test reports. | 02/17/2025 |
| 1668 | Worldwide Clinical Trials San Antonio, TX Research Associate 1 Bachelor’s Degree (preferably in the field of Life Sciences or Health) Exp: 6 months |
The Research Associate 1, has have familiarity with processing and reviewing clinical documentation, interacting with participants, and accommodating competing priorities in a dynamic clinical research environment. | 02/17/2025 |
| 1669 | Worldwide Clinical Trials San Antonio, TX Senior Scientific Associate, Biomarker Analysis Bachelor’s or Master's degree Exp: 0-1 years |
As a Senior Scientific Associate in Biomarker Analysis, you will be a key contributor to our bioanalytical team. Your role involves method development, validation, and sample analysis for ligand binding assays. You’ll work closely with the supervisor to ensure accurate and efficient execution of bioanalytical processes. If you’re passionate about advancing bioanalysis research and have a strong foundation in bioanalysis, this role is for you. | 02/17/2025 |
| 1670 | WuXi AppTec Marietta, GA Associate Laboratory Technician Bachelor’s Degree Exp: 1 year |
Perform Sterility Testing in compliance with applicable Regulations, International Standards following SOPs in cleanroom type environment, perform QA/QC tasks, prep carts. | 02/17/2025 |
| 1671 | HD Biosciences (WuXi AppTec) San Diego, CA Research Associate II Bachelors in Biology related field Exp: 1-3 years |
Assisting and performing efficacy and PK-PD studies and developing new in vivo/ ex vivo assays and models with minimum supervision, as needed. Help to design, optimize and execute of pharmacology experiments for compound screening, compound mode of action and efficacy in mechanistic and disease models, e.g. syngeneic and xenograft tumor model, acute and chronic autoimmune/inflammatory conditions, and analyses and reporting of experiments or implantation, blood/tissue collection, etc. Assist with and perform other experiments as required. Working with the team to perform assay development, optimization, and validation projects. Following SOPs to perform compound receiving, registration, and management. Help to manage lab coordination. | 02/17/2025 |
| 1672 | WuXi AppTec Plainsboro, NJ Scientist I (Contingent) Master’s degree in Chemistry, Biology, or related Physical science Exp: 1-2 years |
With supervision serve as study director/principal investigator to perform MD, MV/MQ and Sample analysis for Large Molecule (LM) Bioanalysis projects. Troubleshoots Wet Lab LM Bioanalysis assays issues and assist in training of LM analysts on wet lab LM systems. Can communicate; write responses to QC/QA findings. Communicate with Clients on specific projects that they are responsible. Accountable for accurate data submission and on time delivery of assigned projects. | 02/17/2025 |
| 1673 | HD Biosciences (WuXi AppTec) San Diego, CA Research Associate II Bachelors in Biology related field. Exp: 0-1 years |
Assist with in vivo pharmacology experiments for preclinical contract research. Perform histology and immunohistochemistry work and other special stains, when needed. Schedule studies, review protocols, data and reports. Establishes scientific standards and new initiatives. Write and review SOPs. Enter data in study management software. Participates in drafting quotations. Develop, implement, optimize, and validate animal models in different disease areas. Effectively communicate with internal colleagues and external clients to promote a world-class service. | 02/17/2025 |
| 1674 | WuXi Advanced Therapies Philadelphia, PA Quality Control Environmental Monitoring Associate I Bachelor’s degree with a major in Biology, Microbiology, or related Life Science Exp: 0-3 years |
Typically, you are either supporting an operation or doing routine sampling. Routine sampling can be performed usually at any point during the day while supporting an operation will have set start and end times when the technician would have to be available. The position is 50% on your feet sampling, 25% lab work, and 25% desk work. The overall schedule tends to change on a day to day basis, this is based off of manufacturing – some of their runs are based on donor material that they don’t always have, some of the runs change based on cell counts, and some of the runs get moved around due to materials and personnel. | 02/17/2025 |
| 1675 | WuXi AppTec Philadelphia, PA Manufacturing Associate I Bachelor’s (science preferred) degree Exp: 0-2 years |
Responsible for manufacture of Master and Working Cell Banks and performing activities within production facilities to support manufacture of Cell & Gene Therapy products, and final product fills according to current Good Manufacturing Practices (cGMPs). | 02/17/2025 |
| 1676 | Abbott Sylmar, CA Product Engineer II – Remote Care Operations Bachelor's Degree Biomedical Engineering or Science, Technology, Engineering and Mathematics (STEM) related Bachelor's degree Exp: 1-2+ years |
The Associate Remote Care Product Engineer is responsible for understanding the integrated set of standards, sub-standards, and assemblies needed to provide remote care support for Abbott CRMD devices. Applies an interdisciplinary, collaborative approach to plan, design, develop and verify a life-cycle balanced system of systems and system/subsystems solution(s) which satisfies customer/operational needs and public/regulatory acceptability. Troubleshooting complex systems and interactions with the full line of remote care capable Abbott devices and supporting hardware will be the primary focus. | 02/17/2025 |
| 1677 | Abbott St. Paul, MN Associate R&D Engineer - Clinical Engineering Bachelor's degree in Engineering (BSME or BSBME preferred) Exp: 1 year |
The Associate R&D Engineer - Clinical Engineering is responsible for evaluating new product designs and understanding how they interact with the user and patient. | 02/17/2025 |
| 1678 | Abbott Temecula, CA Associate TPM Project Engineer Bachelor’s degree in engineering, science or closely related discipline Exp: 0-3 years |
The Associate TPM Project Engineer is an engineering professional who applies scientific knowledge, engineering knowledge, mathematics, and ingenuity to complete assignments related to a specific technical field or discipline. | 02/17/2025 |
| 1679 | Abbott St. Paul, MN Development Quality Engineer II Bachelor level degree in an Engineering Discipline or other Technical Field Exp: 0-2 years |
We are seeking a high caliber Development Quality Engineer II. A development quality engineer assures new or iterative products conform to requirements and establish compliance with the quality system. This position is responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success by protecting patient/user safety and meeting business needs. Each employee can make a difference at Abbott and has the power, either individually or as a team, to influence the success of the company. We are team-oriented, fast-paced and progressive. We value people with great ideas who partner with others both internally and externally to take action and accomplish goals. | 02/17/2025 |
| 1680 | Abbott Casa Grande, AZ Microbiologist - Nutrition Manufacturing Science related Bachelor’s Degree Exp: 1 year |
This position works out of our Casa Grande, Arizona location in the Abbott Nutrition division. Our Nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow to keeping adult bodies strong and active. Millions of people around the world count on our leading brands – including Similac®, PediaSure®, Pedialyte®, Ensure®, and Glucerna® – to help them get the nutrients they need to live their healthiest lives. | 02/17/2025 |
| 1681 | Abbott Plano, TX Development Quality Engineer II Bachelor’s degree in engineering, Technical field Exp: 1-2+ years |
As the Design Quality Engineer II you will assure new or modified products conform to quality standards and establishes compliance with the quality system. Responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success by protecting patient/user safety and meeting business needs. | 02/17/2025 |
| 1682 | Abbott Temecula, CA Quality Engineer Master's degree Exp: 0-2 years |
The Quality Engineer is expected to assist in the identification and resolution of quality related issues. You'll have the opportunity to apply subject matter expertise, in an individual contributor role with limited supervision. Expected to provide quality engineering support to the site to ensure manufacturing/quality requirements are met and understand and elevate issues related to quality validations. Work with a team to establish and implement a dynamic structure that fosters and ensures consistent compliance to external laws, regulations, guidances and standards that affect the quality system. The team will develop and follow a process to implement a structure that will facilitate a consistent implementation of external quality system standards including leading activities for site inspection readiness. This structure will improve coordination between functions and increase the awareness and compliance of external requirements. | 02/17/2025 |
| 1683 | AbbVie North Chicago, IL Associate Scientist II, Oncology Assay Lab Master’s Degree Exp: No exp |
The Oncology Discovery Research team is seeking a highly motivated and experienced Associate Scientist II with expertise in CRISPR genome editing within the Oncology Assay Lab located in Lake County, IL. This is an excellent opportunity for a cell biologist/molecular biologist to make significant contributions to the advancement of oncology drug discovery programs within a dynamic and collaborative environment. The selected individual will play a crucial role in generating high-quality drug development candidates targeting promising therapeutic areas in oncology. An important responsibility will be to investigate, identify, develop, and optimize new methods and techniques. This role will be part of a team of supporting multiple Oncology Discovery programs and projects. | 02/17/2025 |
| 1684 | AbbVie South SF, CA Associate Scientist I/II, Biologics Drug Product Development Bachelor’s degree Exp: 0-3 years |
The Biologics Drug Product Development group within AbbVie is a global organization responsible for developing and characterizing drug product formulations and manufacturing processes for biologic therapeutics (antibodies, antibody-drug conjugates (ADCs), neurotoxins, and novel biologic formats) from preclinical development through clinical proof of concept. We have an exciting opportunity available for an Associate Scientist I/II to join our team at our Bay Area site in South San Francisco, CA. This position requires an onsite presence and involves lab-based functions. Successful candidates will thrive in a collaborative lab environment. | 02/17/2025 |
| 1685 | AbbVie Westport, MO NPI QC Bioassay Trainer Bachelors or Master’s Degree of Science Exp: 1-3 years |
We are now hiring an NPI QC Bioassay Trainer into our team in Westport for a Fixed Term Contract for 23 months Fixed-Term-Contract. This person will join the Westport Bioassay department and the role centres on providing an efficient training programme to all personnel working in the QC Bioassay labs. The trainer role will be responsible for developing and managing training of all new hires for NPI QC Bioassay and will be responsible for updates to key stakeholders on training timelines to support analyst training completion on time. The trainer role will also include supporting NPI drug product stability testing, ad-hoc investigational & development testing. There may be a requirement to execute/assist on new method transfers and validations. To support this volume of testing, ancillary laboratory duties including critical reagent screening/qualifications, laboratory housekeeping, review of paperwork and procedural updates are required. | 02/17/2025 |
| 1686 | AbbVie North Chicago, IL Associate Scientist II, Analytical R&D Master’s Degree in chemistry, Analytical Chemistry, or equivalent education Exp: No exp |
For the Associate Scientist II position, we are seeking a highly motivated candidate who can independently generate precise, reliable and reproducible data in a timely manner. Can demonstrate experimental precision and strong data interpretation skills. He/she should possess understanding of core discipline and support early phase development of New Chemical Entities (NCEs) drug substance and drug product in both preclinical and clinical programs. Collaborate within the global Analytical R&D organization and with R&D cross-functional partners such as Pre-Clinical Safety (PCS), Process Chemistry, Process Engineering, Drug Product Development (DPD), and Quality Assurance (QA) and CMC-Regulatory. | 02/17/2025 |
| 1687 | Strand Therapeutics Boston, MA Associate Scientist, In Vivo Discovery B.S. or M.S. in Biological Sciences, Bioengineering or related discipline Exp: 1-3+ years |
We are looking for an Associate Scientist to join the In Vivo Discovery group to conduct proof-of-concept, validation, and pharmacology studies to support multiple pre-clinical programs. You will be passionate about scientific discovery, undeterred by bold challenges, and enjoy working as a team to develop the next generation of mRNA medicines. You should be highly organized, a critical thinker, adaptable to changing priorities, and possess a strong ability to collaborate effectively with teams of diverse backgrounds. | 02/11/2025 |
| 1688 | Sun Pharma Billerica, MA Process Development Scientist I BS in related scientific major Exp: 1-3 years |
Provides support for new product formulation, aseptic & topical process development, process transfers and troubleshooting existing manufacturing processes. | 02/11/2025 |
| 1689 | SBI Palo Alto, CA Technical Support Specialist (TSS) Master's in a life sciences field (Molecular Biology, Cell Biology, Biotechnology, or a related field) Exp: 1-2 years |
As a Technical Support Specialist, you'll play a critical role in empowering researchers worldwide. You'll work closely with scientists to provide expert guidance, troubleshoot technical issues, and contribute to product development. | 02/11/2025 |
| 1690 | SystImmune Inc Redmond, WA Research Associate/Senior Research Associate BS or MS in immunology, biochemistry, molecular biology, structural biology, or a related field Exp: 1+ year |
We are seeking a skilled Research Associate/Senior Research Associate with experience in utilizing display technologies (yeast/phage) in protein engineering, directed evolution, or binder discovery. This is a laboratory-based role that will be supporting protein engineering efforts in discovering novel binders and novel protein leads/scaffolds. The position will join a growing protein engineering team in an innovative organization and reports to the Director of Protein Engineering. The ideal candidate will be a quick learner with a broad experience set with direct expertise in a display technology and/or an adjacent field including but not limited to high throughput molecular biology, antibody/binder discovery, and protein engineering. Industry experience in biologics drug development is required. | 02/11/2025 |
| 1691 | SystImmune Inc Redmond, WA Research Associate/Senior Research Associate - Cell Science Bachelor’s degree in biology or a related science major Exp: 1+ year |
We are seeking a Research Associate / Senior Research Associate with experience in cell culture and plasmid preparation to join our Cell Science Department. | 02/11/2025 |
| 1692 | Takeda Boston, MA Senior Research Associate - Binding MS in scientific discipline Exp: 1+ years |
The Global Biologics Biological Generation and Analytics team seeks an enthusiastic, energetic, and team-oriented individual to join us. The position involves contributing to the team by identifying binding interactions through various techniques and independently analyzing data. Responsibilities include designing and executing experiments, troubleshooting as needed, and actively participating in program teams to develop analytical strategies. Effective communication skills and the ability to work within cross-functional teams are essential. | 02/11/2025 |
| 1693 | Takeda Boston, MA Research Senior Associate, Inflammation (GI2) Drug Discovery MS in a scientific discipline Exp: 1+ years |
The Gastrointestinal and Inflammation (GI2) Drug Discovery Unit at Takeda is building a new team of experienced, innovative, and collaborative researchers to deliver an industry-leading portfolio of drugs for various gastrointestinal, autoimmune, and inflammatory diseases with high unmet medical needs. We seek a skilled Research Senior Associate to join our biology and cross-functional discovery teams and create novel drug candidates. | 02/11/2025 |
| 1694 | Takeda Thousand OAks, CA Quality Analyst Bachelor’s degree in chemistry or Biological Sciences Exp: 1 year |
The Quality Analyst will be responsible performing the daily quality operations for Quality Lab Services within the Quality organization. You will manage stability management, basic investigation activities, coordinating external lab testing, managing analytical instrument preventive maintenance, inventory management, compiling critical quality attributes data for the Product Quality review and Yearly Biologic Product Report, initiating deviations, and participating in quality process improvements for the QC labs. You will report to the AQC Manager. | 02/11/2025 |
| 1695 | Takeda Brooklyn Park, MN Development Associate II Master’s degree in a scientific discipline Exp: 0-3 years |
As a Development Associate II, you will work with other members of the Technical Operations group to lead tech transfers of products into the facility at bench and pilot scale and subsequently to commercial scale. You will provide manufacturing technical support including batch records, deviations, change controls, investigations, life cycle management, scale down modeling, satellite runs, process validation, data tracking and trending, and supporting CMC regulatory filings. You will report to the Senior Manager of Technical Operations. | 02/11/2025 |
| 1696 | Takeda Boston, MA Research Senior Associate, Oncology Drug Discovery Unit MS in a scientific discipline (or equivalent) Exp: 1+ years |
Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Research Senior Associate, Oncology Drug Discovery Unit in our Cambridge office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. | 02/11/2025 |
| 1697 | Takeda Cambridge, MA Research Associate, Binding and Characterization MS or BS degree in scientific discipline Exp: 1 year |
The Global Biologics Biological Generation and Analytics team seeks an enthusiastic, energetic, and team-oriented individual to join us. The position requires technical understanding of binding interactions and instrumentation used for binding, BLI and SPR. Individual will be responsible for understanding and interpreting data generated. The individual will be required to work with peers to design and implement binding experiments. This position requires the ability to perform in team setting. | 02/11/2025 |
| 1698 | Tanvex San Diego, CA QC Associate, Quality BS or advanced degree in chemistry, biology, biochemistry or related life sciences discipline Exp: No Exp |
The Quality Control Associate I, is responsible for supporting the control and management of samples within QC and performing routine testing of in-process, release, and stability samples following written methods and procedures. The position will work as part of the Analytical Development (AD) / Quality Control (QC) group to support the team responsibilities. Adherence to GMP/ GDP guidelines and ability to follow SOP’s is required. | 02/11/2025 |
| 1699 | TE Connectivity Atlanta, GA Staff Field Application Engineer Bachelor’s Engineering Degree in one of the academic discipline's mechanics, electrics, electronics Exp: 1-3 years |
TE Connectivity’s Field Application Engineering Teams work intimately with customers to recommend products and solutions for new and existing applications. They identify new applications, requirement modifications and enhancements to meet customer specifications and conduct on-site installation and service of product and are responsible for all technical aspects of the sales cycle for potential application of company products to meet customer needs, including identifying opportunities; determining solutions; creating demand; preparing detailed product specifications and technical marketing support; ensuring high quality and timely project execution and conducting follow-up technical support. They also approve operational quality of systems and equipment. | 02/11/2025 |
| 1700 | TE Connectivity Middletown, PA R&D/Product DVL Engineer I BA/BS degree or higher in mechanical engineering Exp: 0-3 years |
TE Connectivity’s R&D/Product Development Engineering Teams conceive original ideas for new products, introduce them into practice. They are responsible for product development, and qualification from market definition through production and release; assist in the qualification of suppliers for new products to ensure suppliers deliver quality parts, materials, and services for new or improved manufacturing processes; conduct feasibility studies, testing on new and modified designs; direct and support detailed design, testing, prototype fabrication and manufacturing ramp. The R&D/Product Development Engineering Teams provide all required product documentation including, but not limited to, Solid Model, 2D/3D production drawings, product specifications, and testing requirements. They create and modify detailed drawings and drafting or conceptual models from layouts, rough sketches or notes and contribute to design modifications to facilitate manufacturing operation or quality of product. Typical fields of expertise include: materials, mechanics and systems, electrical, optics, chemistry, software, automation systems, packaging, testing and measurement, and manufacturing of electrical, mechanical and electronic components, products, and their integration into systems. | 02/11/2025 |
| 1701 | TE Connectivity Mansfield, OH Research & Development Product Development Engineer II Bachelor’s Degree in Engineering, E.E. Exp: 1-5 years |
The R&D/Product Development Engineering is responsible for the design, development of product line extensions of legacy product, with a focus on sustaining engineering of contactors/relays, power distribution panels and related products for applications in aerospace electrical power distribution and management systems. The ideal candidate should be able to work independently and within a team-based environment. Determine product requirements based on internal/external product design specifications and Voice of the Customer inputs. Plan and record results of design, development, and sustaining activities, including validation testing. Design to cost target while meeting financial and performance expectations. Manage Bill of Materials for products. Facilitate cost reduction activities on new and existing products. Perform calculations, analysis, and testing to ensure that a product meets specifications. Participate in and/or lead Design and Process failure mode and effects analysis. Provide support to both internal manufacturing, quality, Product/Project Managers, and external customers. Initiate and manage engineering change activities. Apply electrical, electronic, and mechanical principles to components, including assembly, analysis, and documentation of results. Supports, participates, and leads design, test, modification, fabrication, and assembly of prototype devices. | 02/11/2025 |
| 1702 | Tempus Durham, NC Molecular Technologist I-IV BS/BA or MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Perform routine testing, quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform next-generation sequencing, including nucleic acid extraction, DNA/RNA quantification and qualification, NGS library preparation, probe hybridization, probe/library capture, library cleanup and quantification, loading sequencing libraries onto the Illumina Nextseq, HiSeq4000, and Novaseq. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Obtain 12 continuing education hours in the field of oncology or molecular biology. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 02/11/2025 |
| 1703 | Tempus Chicago, IL Quality Control Technologist I-III BS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work within a cutting-edge genomics workflow to provide quality control support in a high-volume clinical molecular laboratory. Help create and implement new equipment functionality for use by Tempus R&D and clinical lab staff while maintaining CLIA/CAP/NYS-DOH/ISO compliance. Test and document new lots of reagents for clinical lab team processing and label reagents approved for use. Maintain reagent qualification records and manage quality control of reagent inventory. Collect and help analyze metrics. Complete Performance Qualifications (PQs), Preventive Maintenance (PM), relocation, and routine maintenance for all clinically approved molecular laboratory equipment. Investigate issues and help facilitate and implement corrective and preventative actions. | 02/11/2025 |
| 1704 | Tempus Chicago, IL Research Associate BS or MS degree in Immuno Oncology, Cellular or Molecular Biology or related field Exp: 1-2+ years |
We are looking for a highly skilled Research Associate to join our Biological Modeling team within the Biorepository. Our CAP accredited Biorepository develops complex, microenvironment-rich human tumor models for use in a range of studies with our academic and pharmaceutical partners to develop next generation cancer therapies. The ideal candidate will have a strong understanding of immuno-oncology, cell biology and experience with sterile tissue culture and molecular techniques. Prior laboratory experience with mouse and human primary cells and training in CRISPR gene editing approaches is preferable. The successful candidate will be responsible for developing, maintaining and archiving tumor organoid cultures, as well as working with multidisciplinary teams supporting functional assays. | 02/11/2025 |
| 1705 | Tempus Chicago, IL Molecular Technologist I-IV BS or MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Perform routine testing, quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform next-generation sequencing, including nucleic acid extraction, DNA/RNA quantification and qualification, NGS library preparation, probe hybridization, probe/library capture, library cleanup and quantification, loading sequencing libraries onto the Illumina Nextseq, HiSeq4000, and Novaseq. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Obtain 12 continuing education hours in the field of oncology or molecular biology. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 02/11/2025 |
| 1706 | Tempus Chicago, IL Molecular Technologist (Wed-Sat PM Shift) BS or MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Perform routine testing, quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform next-generation sequencing, including nucleic acid extraction, DNA/RNA quantification and qualification, NGS library preparation, probe hybridization, probe/library capture, library cleanup and quantification, loading sequencing libraries onto the Illumina Nextseq, HiSeq4000, and Novaseq. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Obtain 12 continuing education hours in the field of oncology or molecular biology. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 02/11/2025 |
| 1707 | Tempus Chicago, IL Molecular Technologist I-II (3rd Shift) BS or MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Perform routine testing, quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform next-generation sequencing, including nucleic acid extraction, DNA/RNA quantification and qualification, NGS library preparation, probe hybridization, probe/library capture, library cleanup and quantification, loading sequencing libraries onto the Illumina Nextseq, HiSeq4000, and Novaseq. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Obtain 12 continuing education hours in the field of oncology or molecular biology. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 02/11/2025 |
| 1708 | Tenaya Therapeutics Union City, CA QC Analyst (Contract) Bachelor’s or master’s degree in biology, Biochemistry, or a related field Exp: 6 months |
In this role, you will support QC GMP operation and key assays for release, in-process, and stability testing; Other activities include but not limited to data trending, archiving, lab/equipment maintenance, reagent preparation/supplies ordering, supporting EM and microbiology testing. Final job title will be determined based on candidate experience level. | 02/11/2025 |
| 1709 | Terumo Medical Corporation Elkton, MD Quality Engineer I Bachelors degree in engineering, engineering technology, computer science, mathematics, or physics Exp: 1 year |
The position as a Quality Engineer will work closely with the Operations and Engineering Teams to ensure that goods and current products are well designed and manufactured to meet or exceed the customer expectations and requirements. This position will support manufacturing production and is responsible for performing corrective actions and driving continuous improvement initiatives. Ensure compliance to Terumos quality policy, respond to customer complaints, perform audits, develop test methods, and/or write procedures for material characterization. | 02/11/2025 |
| 1710 | Tessera Therapeutics Somerville, MA Research Associate I, High Throughput Oligonucleotide Chemistry BS/MS degree in Chemistry, Biology or related field Exp: 0-1 year |
Tessera Therapeutics is looking a Research Associate to support upstream processes for Oligonucleotide manufacturing, research and scale -up. You are interested in gaining a deep understanding of organic synthesis techniques and finding efficient ways to synthesize long oligonucleotide. You are comfortable multitasking in a fast paced environment under supervision with support of your team on various aspects of the platform. You are an independent, creative thinker with high attention to detail and are enthusiastic about contributing to new ideas. | 02/11/2025 |
| 1711 | Tessera Therapeutics Somerville, MA Research Associate II/Senior Research Associate, Oligonucleotide Foundry MS in chemistry, biology, or related life sciences Exp: 1+ years |
Learning and implementing purification strategies for complex oligonucleotides. Conducting research into alternate purification strategies. Preparing transfer of methods to larger-scale cGMP manufacturing environment. Performing routine operations for critical technology components. Participating in cross-functional teams and training to gain familiarity in all stages of oligonucleotide research and manufacturing | 02/11/2025 |
| 1712 | Tevard Biosciences Cambridge, MA Research Associate, in vivo pharmacology BS/MS in Neuroscience, Physiology, Molecular/Cellular Biology, or a related Life Science discipline Exp: 0-2 years |
We are looking for Research Associate (RA-I or RA-II) with an innovative mindset, great attention to detail and ability to work collaboratively to solve problems, to help advance therapeutic candidates to the clinic. The successful candidate will have an opportunity to positively impact patients with serious unmet medical needs while working closely with our world-class scientific team, including with company’s scientific co-founders In this position, you will collaborate with the in vivo pharmacology team to study effects of therapeutic lead candidates. The RA will work with animal models for rare genetic diseases and will be responsible for executing experiments to quantify molecular, cellular, and physiological readouts, in addition to supporting in vivo dosing studies and related research activities within the in vivo pharmacology group. This is an exciting opportunity for a motivated scientist to further develop their skills in neuroscience, physiology and gene therapy while helping to make an impact on lives of patients suffering from rare diseases. | 02/11/2025 |
| 1713 | Ritedose Columbia, SC Microbiologist I B.S. degree in Microbiology or related field. Exp: 0-1 years |
The Microbiologist I is responsible for all duties related to performing environmental monitoring, personnel monitoring, microbial enumeration, microbial identification, and sampling of utilities. The Microbiologist I is also responsible for performing all the microbiological testing related to raw materials, utilities, and in-process product testing. Other responsibilities include data entry, data review, ensuring calibration of equipment, maintaining and ordering inventory of laboratory supplies, and maintaining the Microbiology laboratory by ensuring its cleanliness and order. | 02/11/2025 |
| 1714 | Theradex Oncology Princeton, NJ Clinical Research Associate I Bachelor's degree in biological or human science-related field Exp: 1 year |
At Theradex, you aren’t just a number. You are part of a highly engaged team of exceptional and supportive people who pride themselves on quality monitoring, continuous learning, challenge themselves and who reap the rewards of providing first in class monitoring to our sponsors. | 02/11/2025 |
| 1715 | Theragenics Buford, GA Process Engineer Bachelor’s degree in engineering, Life Sciences, or a related technical field Exp: 1-3 years |
The Process Engineer is essential to ensuring the seamless integration of manufacturing processes with quality management systems, driving operational efficiency, product excellence, and regulatory compliance. This role combines process engineering expertise to optimize production workflows and resolve technical challenges with quality engineering responsibilities, including maintaining product quality, managing non-conformances, and supporting continuous improvement efforts. This individual is responsible for supporting the development and implementation of robust procedures, track key performance indicators, and ensure alignment with industry standards. A successful Process Engineer will bring strong problem-solving skills, a data-driven mindset, and a proactive approach to identifying and implementing process improvements. | 02/11/2025 |
| 1716 | Thermofisher Worcester, MA Labs FSP Associate Scientist - Separations and Automation Technologies Bachelor's degree in biological or human science-related field Exp: 0-2 years |
In this position as an Associate Scientist, you should possess a thorough understanding of laboratory procedures. You will perform a variety of complex sample preparation and analysis procedures to quantitatively measure biopharmaceutical compounds in a variety of biological matrices. Instrumentation is primarily HPLC and CE. Hamilton Liquid Handlers Protein Maker affinity purification is used as well. Requires following analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against acceptance criteria, methodology, protocol and product specifications. Enters data into databases and reports. | 02/11/2025 |
| 1717 | Thermofisher Cincinnati, OH Quality Specialist II (GMP Investigations) Bachelors Degree in Chemistry, Biology, Engineering or relevant science Exp: 1+ years |
Investigates and observes Operations and Quality Operations departments to assure that FDA current Good Manufacturing Practices, company SOPs and product registrations are followed and maintained. Conducts investigations of batches, preps, lots, equipment, and facilities in accordance with the Code of Federal Regulations. Assists the Operations and Quality Operations departments in satisfying all FDA and DEA requirements. | 02/11/2025 |
| 1718 | Thermofisher Cincinnati, OH Engineer II, Manufacturing Engineering Bachelor’s Degree in Industrial, Manufacturing, Chemical, Mechanical engineering or related field Exp: 1 year |
This role will support manufacturing production through root cause analysis and implementing engineering solutions. The Engineer will identify and complete improvements to current manufacturing processes. Must uses the latest engineering techniques to reduce product time to market whilst adhering to regulatory requirements, project timelines and product costs. | 02/11/2025 |
| 1719 | Thermofisher Middleton, WI Entry Level Scientist (Scientist I) Bachelor's degree (Life Sciences degree preferred) or equivalent Exp: 0-2 years |
As a Scientist I, you will use innovative technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and analysis serve as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. | 02/11/2025 |
| 1720 | Thermofisher Middleton, WI Associate Group Leader - Cell Lab Bachelors degree Exp: 1+ year |
Provides line-level management coordination of resources and work schedules for laboratory activities. Oversees daily operations and assists in preparation and implementation of company policies, quality systems and training programs. Ensures that projects are completed in a timely manner so that company revenues are met and clients are satisfied with the quality and turnaround time of work being performed. Ensures that laboratory staff continues to be developed to keep pace with department goals and growth. | 02/11/2025 |
| 1721 | Thermofisher Richmond, VA Assistant Scientist Bachelor's degree Exp: 0-1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 02/11/2025 |
| 1722 | Thermofisher Middleton, WI Formulation Tech II (High Volume) - 2nd Shift B.S. in Science or Medical Technology Exp: 1 year |
Join Thermo Fisher Scientific as a Large Volume Formulation Tech 2 on our 2nd shift. This position in our Manufacturing division offers a remarkable chance to perform precise techniques and procedures in formulating liquid chemical solutions for reagents, controls, and calibrators. You will work with large volume equipment (1500L – 36000L). | 02/11/2025 |
| 1723 | Tolmar Windsor, CO Manufacturing Operations Engineer I Bachelor’s degree in engineering or similar field Exp: 1+ years |
The Manufacturing Operations Engineer I provides technical support for manufacturing processes for specialty injectable and aseptic products while ensuring those products are made with quality for our patients. The Manufacturing Operations Engineer I assists with protocols and changes for the Manufacturing Department and provides hand-on and technical support for other department projects when dealing with Manufacturing. Owns Quality Event investigations and supports equipment troubleshooting / updating / installing. Manufacturing Operations Engineers are system owners for the Electronic Batch Records (EBR) and Freeweigh systems and serve as the manufacturing technical point of contact for Enterprise Resource Planning (ERP) projects. | 02/11/2025 |
| 1724 | Tolmar Windsor, CO MS&T Engineering Technician (Temporary) BS/MS in scientific or engineering field Exp: 1+ years |
Under general supervision, provides office and laboratory support to the Technical Services group in the MS&T department, which includes a variety of technical documentation activities, administrative activities, product investigation activities, and related tasks. | 02/11/2025 |
| 1725 | Transpire Bio Miami , FL Associate Scientist I/II BSc or MSc in Chemistry, Pharmacy or related fields Exp: 0-2 years |
Conduct laboratory activities with limited supervision including for example analyzing raw materials, in-process materials and finished pharmaceutical products for quality, safety, purity, strength and identity using applicable methods or manufacturing drug product, following the cGMP, EH&S and other relevant guidelines of Corporate, FDA and other governing bodies. Independently set up and operate lab equipment, prepare reagents, solvents and solutions for analytical and formulation activities. Prepare and maintain accurate records in lab notebooks of all testing performed. Process analytical data on lab equipment such as HPLC/UPLC, enter data in spreadsheets and conduct routine calculations. Support the manufacture of inhalation drug product. Prepare samples for blend uniformity. Perform equipment qualification and calibrations as directed. | 02/11/2025 |
| 1726 | Trinity Waltham, MA Research Associate - Value, Access, and Pricing (EVAP) Bachelor’s degree or master’s degree in life sciences Exp: 1-3 years |
We are currently seeking a Research Associate to support Trinity’s Evidence, Value, Access, and Pricing (EVAP) teams with research activities spanning several adjacent areas: Payer / HTA and pricing analysis, life science-related landscape research, targeted and systematic literature review, and research relating to value dossier development. | 02/11/2025 |
| 1727 | SGS Deer Park, TX Chemist Bachelor’s Degree in Chemistry or a related science Exp: 1 year |
Responsible for analysis and reporting of various products such as crude oil, fuel oils, middle distillates, petroleum and petrochemicals, LPG & LNG gases, etc. | 02/05/2025 |
| 1728 | Sharp Packaging Services Allentown, PA Quality Specialist (2nd shift) Bachelor’s degree Exp: 1-3 year |
The Quality Specialist provides quality oversight, GMP guidance and support and makes quality related decisions for the designated functional areas within Sharp Commercial sites. They work closely with internal teams daily and occasionally represent Sharp Quality in customer interactions. The Quality Specialist is responsible to support, design and implement GMP initiatives and continuous improvement opportunities within the Quality Operations organization through data analysis, training, motivation and coaching in collaboration with internal and external stakeholders. Must possess a working knowledge of FDA regulations pertaining to Pharmaceutical /Pharmaceutical Packaging Operations. | 02/05/2025 |
| 1729 | Shennon Biotechnologies San Francisco, CA Research Associate Bachelor’s degree in Molecular Biology, Biology, Biochemistry, Biomedical Engineering or equivalent Exp: 1-3 years |
We are a well-funded early-stage startup based in SF that has created a proprietary single cell platform for the development of more effective cancer immunotherapies. We are looking for a research associate to join our interdisciplinary team. The candidate is expected to learn quickly and communicate well, especially in a fast-paced startup environment. The candidate will work directly with all members of the team. The ideal profile is someone who wants to gain a few years of research experience before going back to graduate school or someone who has just finished college/master's and wants to support scientists in the long term. | 02/05/2025 |
| 1730 | SHL Medical Deerfield Beach, FL AS Engineer B.E. in Biomedical Engineering/Mechanical Engineering or any relevant branch of study. Exp: 0-2 years |
Execute tests, document & analyze test data, write protocols, procedures, equipment work instructions, test instructions. | 02/05/2025 |
| 1731 | Siegfried Grafton, WI Process Engineer Bachelor's degree in Chemical Engineering Exp: 0-5 years |
The incumbent manages all technical aspects of assigned products and/or new processes in manufacturing. This includes preparing batch log records and cleaning log records, supporting production, conducting investigations, implementing corrective actions, and improving yields and cycle times. | 02/05/2025 |
| 1732 | Siemens Charlotte, NC Smart Buildings Associate Energy Engineer Bachelor’s degree in Engineering or related technical field Exp: Entry Level |
The Associate Energy Engineer primary responsibility is driving growth in our Energy Services business by performing and supervising facility site visits/audits, analyzing the customer’s current situation, and developing Facility Improvement Measures (FIMs). This position works closely with Sales in the identification and qualification of Energy Services projects and supports ongoing service agreements. | 02/05/2025 |
| 1733 | Siemens Healthineers Mishawaka, IN Scientist I Bachelor of Science (BSc) or Masters (MS) degree in Chemistry or Organic Chemistry Exp: 1-3 years |
Analyzes and designs work systems in order to support general adherence to agreed standards, in order to ensure humanely and economical production and drives continuous improvement topics. This is a preparative organic chemistry synthesis position at the Siemens Healthcare Diagnostics Mishawaka, Indiana facility; Organic Chemistry Group (OCG). The position requires 70% lab/bench work and 30% office/documentation. ‘Work from home’ is NOT an option for this position. The normal work week is 40 hours. However, additional time may be required to meet specific product delivery and chemistry demands. | 02/05/2025 |
| 1734 | Revvity Remote, PA Associate Customer Service Engineer B.S in Physics or Engineering discipline Exp: 0-2 years |
Revvity is seeking a Customer Support Engineer to join a customer focused field service team in our High Content Imaging Business Unit for the Mid-Atlantic territory (PA, NY & NJ regions). The High Content Imaging Business Unit focuses on the sales of Opera Phenix Plus and the Operetta CLS and related products. The successful individual will provide field service support for the continuously growing High Content Imaging install base in the United States including installations, training, customer training, preventative maintenance, and repair. The individual will also assist with technical support to end-users and field service engineers. | 02/05/2025 |
| 1735 | Revvity San Diego, CA Biochemist I - Bacterial Cell Culture Bachelor of Science in Life Science Exp: 6+ months |
Join our dynamic Molecular Cellular Immunology (MCI) team as a Recombinant Manufacturing Associate, where you’ll play a pivotal role in creating groundbreaking recombinant protein research products. In this hands-on position, you'll be involved in every step of the production process, from recombinant protein expression to purification. Your expertise will be key in tasks like preparing buffer solutions and cell culture media, performing bacterial cultures, and using cutting-edge techniques to affinity purify recombinant proteins. You'll also be responsible for DNA isolation in accordance with established protocols. This role offers exciting opportunities to expand your skill set, with potential additional responsibilities including transferring products to other teams for testing, preparing detailed product and project documentation, and managing inventory and records for recombinant protein products. | 02/05/2025 |
| 1736 | Revvity San Diego, CA Biochemist I - Purification Bachelor’s of science degree in biology, biochemistry, chemistry, or other related area Exp: 1 year |
The Biochemist I will be an integral member of a team that manufactures and provides purified antibodies to enable studies for novel applications in precision medicine, oncology, immunology, neuroscience, and stem cell research. This position will report to a team lead and will ensure the highest quality of our finalized antibody products. This is a great opportunity to work in a fast-paced and dynamic environment for you to enhance your knowledge in the biotechnology industry! In this position you will perform antibody purification via column chromatography both manually and automatically, troubleshooting of problematic errors, continue to improve methodologies for efficiency, follow Standard Operating Procedures (SOP)s, and cross train on a variety of other supporting tasks. | 02/05/2025 |
| 1737 | Revvity San Diego, CA Research Associate II - Product Development Bachelor’s Degree in life sciences Exp: 6+ months |
At BioLegend (a division of Revvity, Inc.) we develop novel, cutting edge products and offer custom services to help with scientific innovation and discovery. We are currently looking for a talented, detail oriented person to join our growing Product Development team. The potential candidate will assist with development of new products for cell analysis such as antibodies, multi-color panels, and reagents for analysis of cell metabolism and cell imaging. The successful candidate must be a self-motivated, team player, able to communicate effectively with a multi-disciplinary team and must possess excellent organization skills. | 02/05/2025 |
| 1738 | Revvity San Diego, CA R&D Materials Coordinator B.S. in Biology, or other biological field Exp: 1-2 years |
Are you ready to kickstart your career in the exciting world of biotech? We’re looking for a motivated and detail-oriented Material Coordinator to join our team! This on-site, entry-level position plays a key role in supporting our corporate business development efforts as we expand our product portfolio through in-licensing, in-house development, and strategic acquisitions. As a Material Coordinator, you’ll be at the heart of our operations, managing the flow of incoming materials. From documenting and receiving to distributing materials to internal stakeholders and external locations, your contributions will directly impact the success of our business. You’ll also work closely with cross-functional teams across Finance, Customer Service, Research and Development, Purchasing, Facilities, and Quality Assurance—making it a truly collaborative experience. This role offers the perfect blend of Biology and Business, providing you with a unique opportunity to learn the ropes of biotech research and development while helping drive forward our company's growth. | 02/05/2025 |
| 1739 | Revvity Lafeyette, CO Associate Scientist- Molecular Biology Bachelor’s Degree in life or natural sciences Exp: 0-2 years |
Revvity has an exciting opportunity for an enthusiastic Associate Scientist for molecular biology/viral production. The Associate Scientist position will perform primary tasks in an ISO 9001:2015 biology manufacturing laboratory in Lafayette, CO. Key responsibilities for this position include a wide array of duties related to the processing and preparation RNAi and Gene Editing products including molecular biology bench work, cloning, viral production, nucleic acid purification, collection replication, inventory control, and order packaging. The position will require the ability to learn and to troubleshoot various aspects of molecular biology and microbiology. | 02/05/2025 |
| 1740 | Revvity Lafeyette, CO Scientific Support Specialist - Hybrid MS in Biological Sciences. Exp: 1-2+ years |
The Scientific Support Specialist helps researchers achieve cutting edge scientific results by providing timely, high-quality support to customers using our full portfolio including Dharmacon brand gene editing, RNAi, cell culture, gene expression & companion diagnostic products. Working as part of our highly experienced technical team, the Scientific Support Specialist will use their scientific expertise daily to guide customers through their full experimental journey: Addressing pre-sales questions and inquiries, troubleshooting problems, and managing complaints in a fast-paced and dynamic work environment. Through in-depth interactions across the company, this role will provide extensive insight into the business world and would be a perfect introduction to the commercial sector for an applicant interested in applying and sharing their scientific knowledge. The position will be ultimately based in our offices either in Lafayette, CO, or Cambridge, UK on a hybrid basis. | 02/05/2025 |
| 1741 | Smithers Darien, IL Associate Chemist I B.S. degree in chemistry or related field Exp: 6 months |
The Associate Chemist I performs critical sample processing and extraction duties to prepare cannabis samples for analysis. The Associate Chemist I enters sample information in the laboratory information management system (LIMS) to facilitate subsequent analysis. The position is responsible for maintenance of laboratory stock reagents. Operates and may maintain, under supervision, test equipment and apparatus. | 02/05/2025 |
| 1742 | Smithers Gaithersburg, MD Associate Scientist- Molecular Biology BA/BS in Biological or Physical Sciences Exp: 6 months |
Smithers PDS LLC (Pharmaceutical Development Services) offers a comprehensive range of pre-clinical and clinical services for all phases of drug development, including support for development of drug delivery devices, and medical and pharmaceutical packaging testing. Our expert scientists perform large molecule bioanalysis, assay development, validation, and sample analysis at our GLP, GCP, and CLIA compliant laboratories. We are seeking a talented Associate Scientist to join our team in the Gaithersburg, MD laboratory. | 02/05/2025 |
| 1743 | Smithers Wareham, MA Associate Chemist I - Environmental Fate and Metabolism B.S. degree in chemistry or related field Exp: 6 months |
Performs a variety of routine tasks and often complex and difficult procedures independently and under supervision, in support of the conduct of normal laboratory operations. Individual is expected to detect and report problems in standardized procedures due to instrumental, sample, or test system failures. Performs a variety of routine, laboratory-based procedures. Responsible for understanding and routinely performing applicable Standard Operating Procedures, study specific protocol procedures and other laboratory assignments. This often includes recording instrument and apparatus readings on standard forms, preparation of test systems and recording and compiling laboratory data in real time in a complete and thorough manner for individual assignments. Responsible for maintaining cleanliness of the labs, storage and chamber areas as well as executing regular maintenance/calibration of equipment used on a regular basis. Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations as well as company policies. Duties are performed with minimal supervision. | 02/05/2025 |
| 1744 | Smithers Gaithersburg, MD Scientist I MS in biology, life sciences, or chemistry field Exp: 1 year |
Smithers PDS is seeking a Scientist to join our team in Gaithersburg, MD. The Scientist performs data analysis and various assays according to SOP with reliability while applying and meeting GLP, GCP, and/or CLIA requirements. This position assists with ensuring that the lab, materials, and equipment are maintained. | 02/05/2025 |
| 1745 | Smithers Wareham, MA Associate Chemist B.S. degree in chemistry or related field Exp: 6 months |
Smithers Cannabis Testing Services division is seeking an Associate Chemist I at our Wareham, MA location. Essential Functions: Cannabis sample processing of flower, concentrates, extracts, and infused products. Cannabis sample extraction & dilutions. Routine maintenance of laboratory equipment and instrument calibration. Wash glassware used by the laboratory. Accurate entry of sample data into LIMS. Production of laboratory reagents and stocks. Additional duties as assigned. | 02/05/2025 |
| 1746 | Smithers Warwick, NY Associate Scientist- Molecular Biology Bachelor’s degree in the chemical, environmental, physical or biological sciences, or engineering Exp: 0-1 years |
The Cannabis Lab Associate Scientist plays a key role in laboratory operations, ensuring accurate and timely handling of cannabis samples for testing. This position is responsible for assisting with sample intake, weighing and preparing samples, and performing physical chemistry tests to support quality control and compliance. Ideal candidates are detail-oriented, possess a strong foundation in laboratory practices, and are committed to maintaining high standards of accuracy and precision. | 02/05/2025 |
| 1747 | Sofie Miami, FL Quality Assurance Specialist (QAS) I Bachelor’s Degree (Scientific / Medical / Quality) Exp: 1-2 years |
The Quality Assurance Specialist I will be responsible for the oversight of the Quality Assurance program and the Quality Management System at the site level. | 02/05/2025 |
| 1748 | Sofie Albany, NY Quality Assurance Specialist I Bachelor’s Degree (Scientific / Medical / Quality) Exp: 1-2 years |
The Quality Assurance Specialist I will be responsible for the oversight of the Quality Assurance program and the Quality Management System at the site level. | 02/05/2025 |
| 1749 | Sofie Somerset, NJ Quality Assurance Specialist I Bachelor’s Degree (Scientific / Medical / Quality) Exp: 1-2 years |
The Quality Assurance Specialist I will be responsible for the oversight of the Quality Assurance program and the Quality Management System at the site level. | 02/05/2025 |
| 1750 | Sofie Decatur, IL Quality Assurance Specialist I Bachelor’s Degree (Scientific / Medical / Quality) Exp: 1-2 years |
The Quality Assurance Specialist I will be responsible for the oversight of the Quality Assurance program and the Quality Management System at the site level. | 02/05/2025 |
| 1751 | Sonosite (Fujifilm) Bothell, WA Regulatory Affairs Associate Bachelor’s degree Exp: 1-2 years |
The Regulatory Affairs Associate requires application of regulatory knowledge and project management skills to oversee international registration of new products. As the Regulatory Affairs Associate, you will also work with Regulatory team members & international teams to drive systems & process improvement activities for integrated regulatory compliance and global submission processes, including labelling, clinical affairs, new product development, international regulatory requirements and other areas as assigned. | 02/05/2025 |
| 1752 | Hologic Marlborough, MA Quality Assurance Engineer 1 - Chemical Compliance Bachelor’s degree in Chemical Engineering or Scientific field preferred Exp: 1+ years |
The Chemical Compliance Quality Specialist is responsible for developing, implementing, and maintaining Quality Management System (QMS) procedures and work instructions related to chemical compliance within the division. This role serves as a liaison between the Corporate Chemical Compliance group and the division, ensuring regulatory and QMS changes are assessed and implemented. The specialist leads the quarterly Chemical Compliance review process, monitors Key Process Indicators (KPIs), and supports product development and engineering teams as a Subject Matter Expert. Additionally, this position involves assessing product compliance, reviewing engineering changes, conducting production record reviews, and performing investigations. | 02/05/2025 |
| 1753 | Southern Biotech Birmingham, AL Quality Control Technician Bachelor’s Degree in Science Exp: 1 year |
We are currently seeking a Quality Control Technician for testing products, such as antibodies and proteins, following SOP’s and ISO requirements. | 02/05/2025 |
| 1754 | Sovereign Pharmaceuticals Fort Worth, TX QC Chemist I BA/BS Chem Exp: 0 years |
The primary function of a QC Chemist is to perform qualitative and quantitative chemical and physical analysis in support of raw materials, in-process samples, components, and finished drug products testing. | 02/05/2025 |
| 1755 | SRI Ann Arbor, MI Research Engineer / Scientist MS in Oceanography, Geophysics, Applied Math, Physics, or Engineering (e.g. ME, Civil, Aero) Exp: 0-5 years |
We are looking for a Research Engineer or Scientist to work as part of an interdisciplinary team on ocean modeling and exploitation of sensor data in an oceanographic context. This position will be on site in Ann Arbor, MI with flexibility for a hybrid work schedule, 2 days on site and 3 days working from a home office. | 02/05/2025 |
| 1756 | Staar Surgical Tustin, CA Product Development Engineer B.S. or Master's in Engineering or Science discipline. Exp: 1-2 years |
Performs activities associated with the development of new ophthalmic lenses and delivery systems and supports existing products and processes in accordance with Design Control procedures. Develops product specifications, manufacturing methods and procedures under supervision. Conducts test protocols, verification and validation activities, and equipment qualifications under supervision. Prepares test protocols and reports, verification and validation reports, and equipment qualification protocols under supervision. Responsible for producing product development documentation in accordance with Good Documentation Practice. Assists in product conceptualization and design and feasibility testing. Documents work in laboratory notebooks and Technical Reports. Other duties as assigned | 02/05/2025 |
| 1757 | Standard Biotools Boulder, CO Quality Control Analyst I Bachelor’s Degree – major in Chemistry, Biology, or related science Exp: 1-5 years |
We are currently looking for a Quality Control Analyst to perform analysis of raw materials, finished product, stability samples, and R&D materials as part of the quality team. This will include understanding the basics of proteomics and DNA, handing sensitive materials, performing statistical analysis on results, and technical writing to report results as part of supporting multiple departments to achieve a common goal | 02/05/2025 |
| 1758 | Starkey Eden Prairie, MN Firmware Engineer II MS in Electrical Engineering or related field Exp: 1+ years |
The primary objective of the firmware engineering position is to apply their knowledge of embedded systems, digital signal processing, and wireless communications to create, test, and maintain firmware for hearing aid and accessory products. As a member of the firmware engineering department firmware engineers operate in the scope of New Product Development Projects and Advanced Development Projects. They engage regularly with other product development teams to deliver high quality and on-time hearing products to the market. A firmware engineer works under general supervision; developing and communicating solutions to routine technical problems of ample scope. They contribute to the completion of detailed technical tasks. Failure to achieve the desired results can be overcome but may cause delays in program schedules. | 02/05/2025 |
| 1759 | Starkey Eden Prairie, MN Electrical Engineer II - Electroacoustic Engineering Master of Science in Electrical Engineering or related field Exp: 1 year |
The Electrical Engineer II, under general supervision, are responsible for the design of new products and ensuring that they meet performance, quality, manufacturing, and cost requirements for Standard (Behind the Ear - BTE) and/or Custom (In the Ear - ITE) products. Must possess communication ability, technical expertise, creativity, and internal drive to lead the creation of designs that are recognized as best- in-class in the hearing aid industry. Must be able to work well in a team environment and have a passion for continuous improvement. | 02/05/2025 |
| 1760 | STERIS Hauppauge, NY Technical Support Specialist - Software 1 Bachelors degree in one of the related fields: Engineering, Audio/Video, Computer Science, MIS, CIS or related field Exp: 1 year |
As a Technical Support Specialist- Software Integration you will provide technical support to Customers, Partners and the Field Service Team to drive complete resolution of first response and moderately complex issues, along with providing Part Identification assistance. You will be expected to quickly address all incoming inquires delivering timely “service by phone” while delivering an overall extraordinary Customer experience. You must manage the situation to de-escalate while resolving the issue(s). As a specialist you will leverage remote diagnostics, your experience with the products, understanding of the theory of operation/safety hazards for the products and troubleshooting experience to resolve issues quickly. Inquires may include troubleshooting and corrective maintenance advice related to controls, electrical, IT/software, and electronics issues. You will refer complex issues to Product Support Specialists and Senior Service Engineering staff. | 02/05/2025 |
| 1761 | STERIS Spartanburg, SC Quality Analyst Bachelor's Degree in Science or Other Technology Exp: 1-5 years |
The Quality Analyst is responsible for assisting in administration of the quality management system at a site to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. This role leads complaint/CAPA investigations, supplier quality improvement initiatives, continuous improvement initiatives and countermeasures with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. The Analyst also supports production and quality operations by coordinating and performing problem-solving investigations, pre-reviews and final acceptance/run release of processing runs that contain non-conformances. Responsible for the activities related to quality and regulatory compliance to ensure all product processing requirements are met in accordance with Customer specifications including calibrations, dosimetry results, generation of test methods, audits, scheduling, validations, record keeping and reporting. | 02/05/2025 |
| 1762 | STERIS Mentor, OH Lab Based Quality Engineer Bachelor’s Degree (Engineering or related technical field) Exp: 1 year |
Lab-based Quality Engineer dedicated to conducting testing, data mining, data analysis, monitoring, test method development, etc. in support of sustaining product investigations in collaboration with Quality Engineering and R&D teams. Develops and implements methods and procedures for process control, process improvement, testing and inspection to ensure that the products are free of flaws and function as designed. Performs product testing and analysis to maintain quality levels and minimize defects and failure rates. Analyzes reports and defective products to determine trends and recommend corrective actions. | 02/05/2025 |
| 1763 | STERIS Conroe, TX Quality Engineer Bachelor’s Degree Engineering or related technical field. Exp: 1+ years |
The Quality Engineer in our Conroe, Texas facility is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. In this role the Quality Engineer supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 02/05/2025 |
| 1764 | STERIS Sharon Hill, PA Quality Systems Engineer Bachelor's Degree in Engineering General or Other Exp: 1-5 years |
The Quality Engineer is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. This role supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. This position is located in the greater Philadelphia area. | 02/05/2025 |
| 1765 | STERIS Brooklyn Park, MN Quality Analyst Bachelor’s degree in scientific or technical field. Exp: 1-5 years |
At STERIS, the Quality Analyst is responsible for assisting in administration of the quality management system at our Minneapolis site to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. The Analyst also supports production and quality operations by coordinating and performing problem-solving investigations, pre-reviews and final acceptance/run release of processing runs that contain non-conformances. You will be responsible for the activities related to quality and regulatory compliance to ensure all product processing requirements are met in accordance with Customer specifications including calibrations, dosimetry results, generation of test methods, audits, scheduling, validations, record keeping and reporting. | 02/05/2025 |
| 1766 | STERIS Minneapolis, MN Quality Analyst Bachelor’s Degree (Scientific or related technical field) Exp: 1-5 years |
The Quality Analyst is responsible for assisting in administration of the quality management system at our Minneapolis site to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. The Analyst also supports production and quality operations by coordinating and performing problem-solving investigations, pre-reviews and final acceptance/run release of processing runs that contain non-conformances. You will be responsible for the activities related to quality and regulatory compliance to ensure all product processing requirements are met in accordance with Customer specifications including calibrations, dosimetry results, generation of test methods, audits, scheduling, validations, record keeping and reporting. | 02/05/2025 |
| 1767 | Regeneron Tarrytown, NY Process Development Engineer I, Purification Development Master’s degree in either Chemical Engineering, Biochemical Engineering or a related field Exp: 1-2 years |
Regeneron’s Late-Stage Purification Development team within PMPD (Preclinical Manufacturing and Process Development) is seeking an energetic Process Development Engineer I. In this role, you will be responsible for the development, characterization, and transfer of various membrane-based downstream purification processes, including viral retentive filtration, ultrafiltration/diafiltration, and sterile filtration for recombinant proteins, using Quality by Design principles. | 01/28/2025 |
| 1768 | REGENXBIO Rockville, MD Manufacturing Associate Contractor Bachelor’s degree Exp: 0-2 years |
REGENXBIO is currently looking for a highly motivated individual to join our Manufacturing Operations team! As a contract-member of the highly engaged and collaborative group, you will have the unique opportunity to start-up an agile, multi-product, single-use facility. You will be accountable for supporting the establishment of new processes, procedures and ways of working, as well as performing manufacturing process related tasks and unit operations within the Upstream and Downstream areas. | 01/28/2025 |
| 1769 | Renaissance Lakewood, NJ Compounder II, 3rd shift Bachelor’s Degree Exp: 0 years |
Primary Responsibility for execution of bulk product batch processing, inclusive of all process related and administrative activities, as well as Equipment Preparation activities as declared in Compounder 1. | 01/28/2025 |
| 1770 | Renaissance Lakewood, NJ Compounder II, 2nd shift Bachelor’s Degree Exp: 0 years |
Primary Responsibility for execution of bulk product batch processing, inclusive of all process related and administrative activities, as well as Equipment Preparation activities as declared in Compounder 1. | 01/28/2025 |
| 1771 | Renaissance Lakewood, NJ Compounder II, 1st shift Bachelor’s Degree Exp: 0 years |
Primary Responsibility for execution of bulk product batch processing, inclusive of all process related and administrative activities, as well as Equipment Preparation activities as declared in Compounder 1. | 01/28/2025 |
| 1772 | Repligen Corporation Bridgewater, NJ Laboratory Support Specialist Bachelor’s degree in a related field (e.g. Biology, Chemistry) Exp: 1 year |
The VPT Support Specialist is responsible for providing technical assistance and expertise to the CTI/Repligen sales force and customers related to the laboratory instrumentation its sells and supports. The laboratory technology developed and marketed by CTI/Repligen includes variable path length UV/Vis spectroscopy instrumentation. The systems are sold primarily into the pharmaceutical and biotech industry and are commonly used for quantifying concentrations of proteins and antibodies in drug discovery and development, manufacturing, and quality assurance. The VPT Support Specialist will provide support both at CTI/Repligen and on site at customer locations. The type of support will include system qualifications for Installation and Operation (IQOQ), product testing, system maintenance and customer training. Delivering training and support will involve travel to customer locations both domestic and international. Training will be provided by CTI/Repligen. | 01/28/2025 |
| 1773 | Repligen Corporation Raleigh, NC Laboratory Support Specialist Bachelor’s degree in a related field (e.g. Biology, Chemistry) Exp: 1 year |
The VPT Support Specialist is responsible for providing technical assistance and expertise to the CTI/Repligen sales force and customers related to the laboratory instrumentation its sells and supports. The laboratory technology developed and marketed by CTI/Repligen includes variable path length UV/Vis spectroscopy instrumentation. The systems are sold primarily into the pharmaceutical and biotech industry and are commonly used for quantifying concentrations of proteins and antibodies in drug discovery and development, manufacturing, and quality assurance. The VPT Support Specialist will provide support both at CTI/Repligen and on site at customer locations. The type of support will include system qualifications for Installation and Operation (IQOQ), product testing, system maintenance and customer training. Delivering training and support will involve travel to customer locations both domestic and international. Training will be provided by CTI/Repligen. | 01/28/2025 |
| 1774 | Repligen Corporation Lebanon, NH Associate Scientist - Quality Control Bachelor's Degree with experience in a scientific environment Exp: 1-3 years |
Repligen is seeking an Associate Scientist to join our expanding Quality team. | 01/28/2025 |
| 1775 | Repligen Corporation Marlborough, MA QA Associate I, Hollowfiber BA/BS degree (in a Biological Science, Engineering, or Physical Science) Exp: 0-2 years |
We are currently seeking a QA Associate I to join our Quality team in Marlborough, supporting Hollow Fiber and Single Use ATF Manufacturing. The QA Associate I will actively participate in the Repligen ISO 9001 Quality Management System, reviewing production records and releasing product, as well as supporting other QA team members and areas of work, as needed. The successful candidate will have a positive attitude and be able to communicate effectively. This candidate will be responsible for assisting the QA department to revise/create, file, organize, and review production documents. The candidate will work closely with the manufacturing teams to ensure accuracy of production documentation throughout the production process. This position involves completing the QA review of production records, including but not limited to; verification of raw materials used, verification of calculations, good documentation practices, and processing steps have been completed according to the internal processes. | 01/28/2025 |
| 1776 | Repligen Corporation Anaheim, CA Automation Engineer B.S. Degree in Mechanical, Electrical, Computer Science, Industrial Engineering Exp: 1-3 years |
The automation engineer will report directly to the R&D Automation lead. | 01/28/2025 |
| 1777 | Replimune Framingham, MA Manufacturing Associate I/II Bachelor’s degree Exp: 1-3 years |
The Manufacturing Associate I/II is responsible for executing the cGMP manufacturing operations to support the production of Replimune products at the Framingham, MA, facility. This individual will collaborate with multiple departments to support the manufacturing production facility. They will assist with the generation/revision of Standard Operating Procedures and associated documentation to ensure manufacturing readiness. | 01/28/2025 |
| 1778 | Replimune Framingham, MA Sr. Associate, Technical Operations Master’s degree in chemical or biomedical engineering or equivalent Exp: 0-3 years |
The Technical Operations Engineer I/II will be responsible for providing drug substance and/or drug product technical support for oncolytic virus manufacturing. This includes life cycle management of commercial processes, including ownership and support of change controls, CAPAs and deviations. | 01/28/2025 |
| 1779 | Replimune Framingham, MA Manufacturing Technician Bachelor’s degree Exp: 0 years |
Reporting to the Manufacturing Manager, the Manufacturing Technician will be part of a cohesive team responsible for producing RPX at Replimune’s Framingham Manufacturing Facility. The Manufacturing Technician will support production processes by operating, set up, changeover, and cleaning of various automated and manual equipment in strict accordance with SOP’s, Good Manufacturing Practices, and Safety policies/procedures. The manufacturing Technician will support the Manufacturing Team in day-to-day operations. | 01/28/2025 |
| 1780 | Replimune Framingham, MA Manufacturing Specialist I Master’s degree Exp: 0-2 years |
The Manufacturing Specialist I and II will be part of a cohesive team responsible for producing RPX at Replimune’s Framingham Manufacturing Facility. The Manufacturing Specialist uses expert knowledge of cGMP regulations and biopharmaceutical production processes to provide day to day operational support through the implementation of process improvements, leading manufacturing activities, supporting the scheduling of daily manufacturing activities and deviation/CAPA/change control writing with a focus on but not limited to Commercial/Clinical Manufacturing. | 01/28/2025 |
| 1781 | Resolution Medical Fridley, MN Product Development Engineer II - Test Method Bachelor’s degree in related field Exp: 1-3 years |
Activities include product design and development, defining technical solutions to abstract problems, defining methods and processes, design modeling, tooling design/fabrication, equipment design/fabrication, personnel management, design verification and validation, and documentation. Participate in the day-to-day execution of reliability tasks by teams and team members through monitoring progress, providing technical direction, and problem-solving solutions. Subject matter expert on test method development and design verification. Primarily by driving the testing of device, assist in design and develop innovative products & manage the product design from concept to full production. This position will participate in the execution of development projects as part of a multi-functional project team with an emphasis on the V&V activities. | 01/28/2025 |
| 1782 | Restor3d Wilmington, MA Manufacturing Engineer Bachelor’s Degree in Engineering Exp: 0-2 years |
The Manufacturing Engineer I will be responsible for the selection, development, qualification, and scale-up of production processes and equipment across different manufacturing departments. Process objectives are the high quality, high volume production of patient-tailored implants and associated instruments. | 01/28/2025 |
| 1783 | Retro Redwood City, CA Research Associate M.S in Biology or related field Exp: 1 year |
We are hiring a new member of the Microglia Therapeutics team who will be involved in making iPSC-derived microglia, characterizing them, and developing them into cellular therapy product. In this role, you will enable the microglia team to move faster and iterate more quickly by increasing the capacity for hands-on work in the lab. | 01/28/2025 |
| 1784 | Revolution Medicines Redwood City, CA Clinical Trial Assistant II, Clinical Operations Bachelor’s degree in biological sciences or related health related field Exp: 1-3 years |
As a Clinical Trial Assistant II in Clinical Operations, initially reporting to the Director Clinical Operations, you will be responsible for acting as a central contact for the clinical study teams and assist with the clinical execution and management to support RevMed clinical trials. | 01/28/2025 |
| 1785 | Revolution Medicines Redwood City, CA Clinical Trial Assistant II - Clinical Operations Process and Systems Bachelor’s degree in biological sciences or health-related field Exp: 0-1 years (CTA I)/1-3 years (CTA II) |
This is a unique opportunity for an entry-level Clinical Operations Professional. As the Clinical Trial Assistant II, Clinical Operations Process and Systems, you will be responsible for acting as an integral member of the Clinical Operations team and will be tasked to support the management of Clinical Operations processes and systems, in support of execution of RevMed’s clinical trials. | 01/28/2025 |
| 1786 | Rion Rochester, MN Research Associate, Analytical Development Bachelor’s or Master’s degree with focus in Biological Sciences Exp: 1+ years |
The Analytical Development Research Associate will contribute to analytical method development, implementation, and validation of methods focused on Rion’s exosome technology. This role will work closely with Rion Quality Control to execute method transfers and support continuous improvement. As such, the candidate will possess the technical skills required to conduct experiments and assays in a wet lab environment involving techniques such as mammalian cell culture, ELISA, RT-qPCR, HPLC and colorimetric/fluorometric-based assays. The Analytical Development Research Associate will be responsible for the execution of experiments, as well as data interpretation and final reporting. The position affords the opportunity to serve as a key member of Rion’s scientific team and contribute to the advancement of exosome therapeutics. The Analytical Development Research Associate will work closely with the Analytical Development Scientists and support the efforts of Quality Control Development. As such, the successful candidate will work in an upbeat, highly collaborative, and dynamic environment. Additional responsibilities associated with this position will involve assisting in day-to-day laboratory operations such as inventory management, procurement, and general laboratory and equipment maintenance. | 01/28/2025 |
| 1787 | Roche Little Rock, AR Field Engineering Specialist - Fort Smith, AR Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Chemistry or related field Exp: 1-2 years |
Roche Support Network is dedicated to providing exceptional support to customers. As a Field Engineering Specialist you will: Showcase your expertise in technical repair and installation for Roche assigned product lines. Offer valuable service to laboratory customers in your assigned territory. Provide routine technical support, on-site service, repair, and installation of Roche products. Serve as a customer contact for technical and service-related issues and perform preventative maintenance. Diagnose and resolve mechanical, hardware, software, and system failures. Document all activities, contribute to quality improvement, and focus on maximizing customer satisfaction. | 01/28/2025 |
| 1788 | Roche Seattle, WA Field Engineering Specialist - Seattle, WA Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Chemistry or related field Exp: 1-2 years |
Roche Support Network is dedicated to providing exceptional support to customers. As a Field Engineering Specialist you will: Showcase your expertise in technical repair and installation for Roche assigned product lines. Offer valuable service to laboratory customers in your assigned territory. Provide routine technical support, on-site service, repair, and installation of Roche products. Serve as a customer contact for technical and service-related issues and perform preventative maintenance. Diagnose and resolve mechanical, hardware, software, and system failures. Document all activities, contribute to quality improvement, and focus on maximizing customer satisfaction. | 01/28/2025 |
| 1789 | Roche Evansville, IN Field Engineering Specialist - Evansville, IN Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Chemistry or related field Exp: 1-2 years |
Roche Support Network is dedicated to providing exceptional support to customers. As a Field Engineering Specialist you will: Showcase your expertise in technical repair and installation for Roche assigned product lines. Offer valuable service to laboratory customers in your assigned territory. Provide routine technical support, on-site service, repair, and installation of Roche products. Serve as a customer contact for technical and service-related issues and perform preventative maintenance. Diagnose and resolve mechanical, hardware, software, and system failures. Document all activities, contribute to quality improvement, and focus on maximizing customer satisfaction. | 01/28/2025 |
| 1790 | Roche Milwaukee, WI Field Engineering Specialist - Milwaukee, WI Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Chemistry or related field Exp: 1-2 years |
Roche Support Network is dedicated to providing exceptional support to customers. As a Field Engineering Specialist you will: Showcase your expertise in technical repair and installation for Roche assigned product lines. Offer valuable service to laboratory customers in your assigned territory. Provide routine technical support, on-site service, repair, and installation of Roche products. Serve as a customer contact for technical and service-related issues and perform preventative maintenance. Diagnose and resolve mechanical, hardware, software, and system failures. Document all activities, contribute to quality improvement, and focus on maximizing customer satisfaction. | 01/28/2025 |
| 1791 | Roche Scranton/Wilkes Barre, PA Field Engineering Specialist - Scranton & Wilkes Barre, PA Bachelor's degree in a relevant field Exp: 1-2 years |
Roche Support Network is dedicated to providing exceptional support to customers. As a Field Engineering Specialist, you will travel and showcase your expertise in technical repair and installation for Roche assigned product lines. You will offer valuable service to laboratory customers in your assigned territory. The role involves routine technical support, on-site service, repair, and installation of Roche products. You will serve as a customer contact for technical and service-related issues and perform preventative maintenance. The position requires diagnosing and resolving mechanical, hardware, software, and system failures. You will document all activities, contribute to quality improvement, and focus on maximizing customer satisfaction. | 01/28/2025 |
| 1792 | Roche Cape Girardeau, MO Field Engineering Specialist - Cape Girardeau, MO Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Chemistry or related field Exp: 1-2 years |
Roche Support Network is dedicated to providing exceptional support to customers. As a Field Engineering Specialist you will: Showcase your expertise in technical repair and installation for Roche assigned product lines. Offer valuable service to laboratory customers in your assigned territory. Provide routine technical support, on-site service, repair, and installation of Roche products. Serve as a customer contact for technical and service-related issues and perform preventative maintenance. Diagnose and resolve mechanical, hardware, software, and system failures. Document all activities, contribute to quality improvement, and focus on maximizing customer satisfaction. | 01/28/2025 |
| 1793 | Roche Birmingham, AL Field Engineering Specialist - Birmingham, AL Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Chemistry or related field Exp: 1-2 years |
Roche Support Network is dedicated to providing exceptional support to customers. As a Field Engineering Specialist you will: Showcase your expertise in technical repair and installation for Roche assigned product lines. Offer valuable service to laboratory customers in your assigned territory. Provide routine technical support, on-site service, repair, and installation of Roche products. Serve as a customer contact for technical and service-related issues and perform preventative maintenance. Diagnose and resolve mechanical, hardware, software, and system failures. Document all activities, contribute to quality improvement, and focus on maximizing customer satisfaction. | 01/28/2025 |
| 1794 | Sanguine San Diego, CA Lab Technician I Bachelor’s degree Exp: 1 year |
The Entry Level Lab Technician I will be responsible for the processing and testing of various blood samples. Sample processing will include, but is not limited to: PBMC, T, B, & NK cell isolations. Other assigned duties may include cell counting, aliquot preparation, accessioning, reagent creation, proper storage, flow cytometry lab services. Initial samples will be from both Leukopaks and blood samples or its derivatives. This role will also require experience with LIMS systems and commercial laboratory operations, including the internal communication of project details with Sanguine personnel as well as the ability to work as a team. | 01/28/2025 |
| 1795 | Sanofi Swiftwater, PA Senior Production Technician - Vaccines Bachelors Exp: 1+ years |
The Senior Production Technician will: Ensure operational area is running as intended to meet all operational goals. Ensures the completion of Environmental Monitoring sampling and corresponding documentation, data entry, and delivery as required during all aseptic processing. Real time review of this documentation. We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world. | 01/28/2025 |
| 1796 | Sanofi Swiftwater, PA Production Technician - Vaccine Bachelor’s degree Exp: 0 years |
Sanofi is seeking a motivated professional candidate to operate within Biologics production and perform manufacturing activities. This is an exciting opportunity for a candidate to develop technical skills and learn about the biopharmaceutical industry. The production technician will operate in a cGMP manufacturing area performing equipment set up and operations tasks to meet all standards for safety, quality, and efficiency. The candidate will perform production in accordance with volume fluctuation, business need, and effective procedures. | 01/28/2025 |
| 1797 | Sanofi Cambridge, MA Associate Scientist - Medicinal Chemistry, Integrated Drug Discovery Bachelor’s Degree Exp: 1 year |
Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. As a Associate Scientist - Medicinal Chemistry, Integrated Drug Discovery, your skills could be critical in helping our teams accelerate progress. Synthetic organic chemist with deep knowledge of organic chemistry principles and modern synthesis methods to design and execute efficient synthetic routes for target compounds and the progression of drug discovery projects. | 01/28/2025 |
| 1798 | Sciex Atlanta, GA Field Service Technician - Atlanta, GA Bachelor's degree (B.S./B.A.) in Life Sciences, Chemistry, or Engineering Exp: No exp |
The Service Technician is responsible for developing the knowledge and skills to support the maintenance, installation and repair of Sciex products at both internal and external customer sites. This entry-level position works under close supervision and mentoring by a manager, regional specialist, and senior engineers within the territory. Tasks are performed independently as proficiencies are developed. This position reports to the District Service Manager and is part of the Field Technical Service organization working remotely to cover Atlanta GA. | 01/28/2025 |
| 1799 | Sedia Biosciences Beaverton, OR QC Assistant Scientist B.Sc. in applicable biological science or chemistry. Exp: Entry Level |
Sedia Biosciences is hiring a QC Assistant Scientist at our Beaverton, Oregon location. At Sedia, we create diagnostic and disease-monitoring products that provide cost effective solutions for rapid, near patient testing. We are currently seeking responsible individuals motivated to help research and develop our future diagnostic products. This position performs simple laboratory activities related to the inspection and testing or raw materials, components, and finished products in a medical diagnostic development and manufacturing environment following specific instructions from more senior Quality Control personnel or by following technical instructions | 01/28/2025 |
| 1800 | LGC Clinical Diagnostics Cumberland Foreside, ME Quality Control Technologist I Bachelor’s degree in Medical Technology (preferred) or related science degree (i.e. biology, chemistry, biochemistry) Exp: 1-3 years |
Follows standardized procedures and prepares samples for testing. Analyzes test results for accuracy, acceptability, and critical limits. Relies on limited independent judgment to plan and accomplish goals. Performs a variety of tasks. A limited degree of creativity and latitude is required. | 01/28/2025 |
| 1801 | LGC Clinical Diagnostics Milford, MA Manufacturing Associate I/II Bachelor’s degree, with a concentration in Biology, Chemistry, or related science Exp: 1-3 years |
The Manufacturing Associate I / II provides direct labor for the manufacturing of high-quality diagnostic products using manual and semi-automated equipment and prepares/completes required documentation on manufacturing procedures. This position is responsible for set-up, calibration, and operation of all manufacturing equipment in accordance with cGMP, POPs, SOPs, Safety, and departmental policies. This position utilizes good judgment and critical thinking skills to make operator level decisions regarding the quality of the products manufactured. | 01/28/2025 |
| 1802 | LGC Clinical Diagnostics Milford, MA Manufacturing Associate II Bachelor’s degree, with a concentration in Biology, Chemistry, or related science Exp: 1-3 years |
The Manufacturing Associate II provides direct labor for the manufacturing of high-quality diagnostic products using manual and semi-automated equipment and prepares/completes required documentation on manufacturing procedures. This position is responsible for set-up, calibration, and operation of all manufacturing equipment in accordance with cGMP, POPs, SOPs, Safety, and departmental policies. This position utilizes good judgment and critical thinking skills to make operator level decisions regarding the quality of the products manufactured. | 01/28/2025 |
| 1803 | SGS Dayton, NJ Lab Analyst I - PFAS Bachelor’s Degree in a Chemistry or similar scientific discipline Exp: 1-2 years |
Our Dayton, NJ laboratory is looking for a laboratory analyst to join their team! The Lab Analyst will prepare and analyze samples with accuracy and precision in accordance to SGS' analytical SOPs. Work independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. Understand and apply basic analytical chemistry principles. Always follow safe laboratory practices and maintain a safe working environment. | 01/28/2025 |
| 1804 | SGS Seabrook, TX Chemist Bachelor’s Degree in Chemistry or a related science preferred Exp: 1 year |
Responsible for analysis and reporting of various products such as crude oil, fuel oils, middle distillates, petroleum and petrochemicals, LPG & LNG gases, etc. | 01/28/2025 |
| 1805 | SGS Lincolnshire, IL Microbiologist I BS degree in Microbiology or related sciences Exp: 0-2 years |
The Microbiologist I works independently on assigned Microbiological projects and conducts analyses of raw materials, finished products, and waters. As a professional scientist, the Microbiologist is expected to work under the guidance of supervisors and managers, develop skills and understanding of laboratory procedures, exhibit technical expertise, be able to document data and report findings; and stay current with Microbiological literature and standards for analyses. You will also conduct analyses of samples in accordance with USP, EP, ASTM, AOAC, FDA, EPA procedures, procedures supplied by the client, and other non-routine procedures as encountered. | 01/28/2025 |
| 1806 | SGS Anchorage, AK Laboratory Analyst Bachelor’s Degree in a Chemistry or similar scientific discipline Exp: 1-2 years |
Our Anchorage, AK laboratory is looking for a Laboratory Analyst to join our team! The Laboratory Analyst prepares and analyzes samples with accuracy and precision in accordance to SGS' analytical SOPs. The Laboratory Analyst works independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. The Laboratory Analyst understands and applies basic analytical chemistry principles. The Laboratory Analyst always follows safe laboratory practices and maintains a safe working environment. | 01/28/2025 |
| 1807 | Pfizer Andover, MA Process Technician-Purification Bachelor's degree Exp: 1 year |
You will support the execution of production according to Standard Operating Procedures and production schedule. Working with interdisciplinary teams, you will implement process improvements and participate in process troubleshooting. As part of technical operations, you will be developing and applying your knowledge of procedures, techniques, tools, materials and equipment. Your receptiveness to new ideas will enhance the team’s ability to achieve goals and targets. You will follow standard procedures to complete tasks and identify process issues or problems that involve direct application of your skills/knowledge. It is your hard work and focus that will help in making Pfizer ready to achieve new milestones and help patients across the globe. | 01/21/2025 |
| 1808 | Pfizer Sanford, NC Manufacturing Quality Support Senior Associate Master's degree in microbiology, chemistry, biological sciences, bioengineering Exp: 1+ years |
The Manufacturing Quality Support Senior Associate provides Quality Assurance (QA) support to clinical, commercial, and contract manufacturing operations. The role ensures adherence to regulatory expectations, safety, and GxP (i.e., Current Good Manufacturing and Documentation Practices).The role is based at the Pfizer Sanford, NC Pfizer Global Supply (PGS) site. | 01/21/2025 |
| 1809 | Pfizer Groton, CT Senior Associate Scientist MS in Chemical, Mechanical, Electrical or Pharmaceutical Engineering, Physics or Engineering Physics, Computer Science, Pharmaceutics, or other relate Exp: 0-3 years |
Pfizer’s Drug Product Design group is seeking team members with a desire to bring new, cutting-edge medicines to patients around the world. Our team members use science and technology to design, characterize and develop drug product formulations from candidate selection to commercial launch. You will be able to leverage your existing scientific knowledge, as well as develop scientific knowledge in new areas, to evaluate the chemical & physical stability, bio-performance and manufacturability of the drug product across a diverse range of therapeutic areas. You will complete experimentation using conventional and continuous drug product manufacturing equipment and participate in multi-disciplinary teams during the formulation development, process scale up, and technology transfer of conventional and continuous processing technologies to our clinical R&D manufacturing sites, as well as our commercial manufacturing sites within the Pfizer Global Supply organization. You will also apply your engineering, additive manufacturing/3D printing, and rapid prototyping skills to improve machine design, develop and apply advanced computational models and data analysis, and advanced sensing capabilities to the drug product manufacturing. This laboratory-based position offers the opportunity for cross-training and growth in multiple technical areas to encourage a flexible working environment. Enjoy the entrepreneurial mindset and infrastructure to develop new technologies and processes for drug delivery and dosage form manufacture while having access to the resources of a larger company. Excellent laboratory and communication skills, attention to detail, the ability to solve technical problems, and the diligence to maintain thorough electronic laboratory notebook records of work performed are required. Finally, this position will challenge you to pursue scientific excellence and creativity, in collaboration with industry-leading experts across multiple scientific disciplines. | 01/21/2025 |
| 1810 | Pfizer Pearl River, NY Associate Scientist - Bioassay Development BS or BA degree in biology or related discipline Exp: 0-2 years |
This is a laboratory-based position within Pfizer’s Vaccine Research and Development (VRD) organization – Analytical Development group. The candidate assists with development of robust analytical assays in support of early vaccine development for a range of moieties such as mRNAs, proteins, and glycoconjugates. Representative assays include, but are not limited to, cell-based assays monitored by Flow Cytometry, Enzyme-Linked Immunosorbent Assays (ELISAs), and Bioplex/Luminex. The candidate also provides analytical support for bioprocess and formulation development by performing routine/non-routine sample testing. Your strong foundation in general scientific practice, principles, and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. It is your focus and commitment that will help in making Pfizer ready to achieve new milestones and help patients across the globe. | 01/21/2025 |
| 1811 | Pfizer Pearl River, NY Associate Scientist BS or BA degree in biology or related discipline Exp: 0-2 years |
This is a laboratory-based position within the Vaccine Research and Development – Analytical Development group. The candidate contributes to the development of robust analytical assays to support early vaccine development for a range of moieties including proteins, mRNA, and glycoconjugates. Assays include but are not limited to cell-based assays such as flow cytometry, enzyme-linked immunosorbent assays (ELISAs), and immunofluorescence. In addition, the candidate provides analytical support for bioprocess and formulation development through characterization testing of preclinical products. Your strong foundation in general scientific practice, principles, and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. It is your focus and commitment that will help in making Pfizer ready to achieve new milestones and help patients across the globe. | 01/21/2025 |
| 1812 | Pfizer McPherson, KS Senior Process Engineer Masters Exp: 0+ years |
The role is to provide senior level engineering business partnership to the packaging and manufacturing operations leaders. The role will partner with operations, engineering, maintenance and reliability teams to drive overall Equipment and Process improvement and key strategic projects. The role must demonstrate ability to accomplish large and complex projects independently, provide engineering expertise and lead structured troubleshooting efforts of major equipment and process-related issues. Analyzes process requirements and evaluates equipment and systems to ensure deliverables meet or exceed process specifications and packaging/manufacturing requirements. Evaluates and recommends new process technologies that optimize performance, are cost effective, and will improve product quality and manufacturing processes. | 01/21/2025 |
| 1813 | Pfizer Rochester, MI Sr. Automation Compliance Engineer Master’s degree Exp: 1+ year |
The Sr Automation Compliance Engineer will have overall responsibility for managing regulatory aspects of the process automation and control systems used in the manufacture of sterile injectable. This position will provide engineering and technical support related to the operation, maintenance, installation, startup/commissioning, testing, and qualification of systems within a sterile injectable manufacturing facility. | 01/21/2025 |
| 1814 | Caris Life Sciences Phoenix, AZ Quality Assurance Technologist, Solid Tumor Bachelor's degree in a science field. Exp: 1 year |
A Quality Assurance Technologist is responsible for a multitude of different tasks within the clinical molecular laboratory including the quality control testing of all molecular reagents prior to use on clinical samples, assisting the product development team with the validation of new assays and training current employees on new assays as well as new employees on established assays. This position is required to be well versed in various molecular techniques that include, formalin-fixed paraffin-embedded tissue macro-dissection, RNA/DNA extractions, PCR, RFLP, DNA methylation analysis, Next Generation sequencing and automated liquid handlers. Quality Assurance Technologists are expected to contribute technically and intellectually to enhance efficiency within the lab while ensuring that the quality of reagents and training program is maintained to the highest standard. This position works under the direction of the Director and follows standard laboratory procedures and policies. | 01/21/2025 |
| 1815 | Caris Life Sciences Phoenix, AZ Pathologist Associate Bachelor’s degree in a field of science Exp: 0-1 year |
The Pathologist Associate is responsible for supporting and assisting the Pathology and Pathology Operations departments in their daily operations. This position will perform tasks needed to be completed in the day-to-day operation. This position also includes performing the tasks of Macrodissection and Microdissection. | 01/21/2025 |
| 1816 | Quest Diagnostics Denver, CO Lab Associate II Bachelor’s Degree Exp: 1 year |
Prepares and organizes samples for testing, for example, sample racking, aliquoting and tube preparation. Responsible for labeling, handling, processing or preparation, and transportation and storage of specimens. Identifies sample problems and assists in resolving appropriately. Demonstrates problem solving ability on service and production issues. Prepares testing equipment and assists with preventive maintenance. Notifies appropriate technical staff of equipment problems. Assists licensed personnel (CA only) or delegated supervisor (non-CA) in the pre-analytic and post-analytic testing activities, other than trainees, in a licensed clinical laboratory. Prepares pre-analytical reagents and controls using automated or fixed volume measuring devices. Submits documentation to appropriate staff for approval to use. Prepares and maintains complete and accurate records of reagents or media using established procedures, formulas, stock solutions and fixed volume measuring devices. Maintains inventory of consumable items including reagents and supplies. Orders, unpacks, logs, dates and stores reagents/supplies upon receipt and properly rotates stock for use. Performs inventory of laboratory items including restocking the benches and equipment inventory. Sorting and accessioning incoming specimens into appropriate LIS, then delivering to designated testing platform/department. Performs data entry or transcribes data from previously recorded results to computer for data reduction and prepares for licensed personnel's review. Tallies workload data and prepares reports as requested. Assists in the performance of quality control procedures. Prepares protocols/logs or other appropriate documents. Identifies specimen problems and demonstrates ability to appropriately resolve or elevate to licensed personnel (CA only) or delegated supervisor (non-CA). Assists a licensed person (e.g.: CLS) with performance of validation verifications and other Research and Development (R&D) activities, as applicable. Trains other Lab Associates. Supports Training Programs, where applicable. Takes initiative in making suggestions to improve efficiency and productivity and provides consistent feedback. Is a resource for process improvement. Demonstrates leadership through accountability and collaboration in daily activities. Answers phones, transfers, or takes accurate messages. Maintains the confidentiality of client information. Helps to ensure the laboratory areas are neat, clean, and o | 01/21/2025 |
| 1817 | Quest Diagnostics Cleveland, OH Lab Associate II Bachelor’s Degree Exp: 1 year |
Prepares and organizes samples for testing, for example, sample racking, aliquoting and tube preparation. Responsible for labeling, handling, processing or preparation, and transportation and storage of specimens. Identifies sample problems and assists in resolving appropriately. Demonstrates problem solving ability on service and production issues. Prepares testing equipment and assists with preventive maintenance. Notifies appropriate technical staff of equipment problems. Assists licensed personnel (CA only) or delegated supervisor (non-CA) in the pre-analytic and post-analytic testing activities, other than trainees, in a licensed clinical laboratory. Prepares pre-analytical reagents and controls using automated or fixed volume measuring devices. Submits documentation to appropriate staff for approval to use. Prepares and maintains complete and accurate records of reagents or media using established procedures, formulas, stock solutions and fixed volume measuring devices. Maintains inventory of consumable items including reagents and supplies. Orders, unpacks, logs, dates and stores reagents/supplies upon receipt and properly rotates stock for use. Performs inventory of laboratory items including restocking the benches and equipment inventory. Sorting and accessioning incoming specimens into appropriate LIS, then delivering to designated testing platform/department. Performs data entry or transcribes data from previously recorded results to computer for data reduction and prepares for licensed personnel's review. Tallies workload data and prepares reports as requested. Assists in the performance of quality control procedures. Prepares protocols/logs or other appropriate documents. Identifies specimen problems and demonstrates ability to appropriately resolve or elevate to licensed personnel (CA only) or delegated supervisor (non-CA). Assists a licensed person (e.g.: CLS) with performance of validation verifications and other Research and Development (R&D) activities, as applicable. Trains other Lab Associates. Supports Training Programs, where applicable. Takes initiative in making suggestions to improve efficiency and productivity and provides consistent feedback. Is a resource for process improvement. Demonstrates leadership through accountability and collaboration in daily activities. Answers phones, transfers, or takes accurate messages. Maintains the confidentiality of client information. Helps to ensure the laboratory areas are neat, clean, and o | 01/21/2025 |
| 1818 | Quest Diagnostics San Juan Capistrano, CA Lab Associate II - Immunology Bachelor’s Degree Exp: 1 year |
This non-licensed position is accountable for assisting with general support for the laboratory, following all applicable policies and procedures. | 01/21/2025 |
| 1819 | Quest Diagnostics San Juan Capistrano, CA Lab Associate II - Hematology Bachelor’s Degree Exp: 1 year |
This non-licensed position is accountable for assisting with general support for the laboratory, following all applicable policies and procedures. | 01/21/2025 |
| 1820 | Pion Billerica, MA Laboratory Scientist Bachelor’s or Master's degree in Chemistry or preferably Biochemistry required Exp: 1+ year |
The Laboratory Scientist is responsible for supporting and executing experimental work to complete analytical service projects and for supporting the development of chemical and biopharmaceutical testing equipment and innovative applications. | 01/21/2025 |
| 1821 | Pledge Therapeutics Canton, MA Research Associate, Immuno-Oncology MS Exp: 1-2 years |
We seek an enthusiastic and curious scientist interested in participating in all aspects of the hit-to-lead drug discovery process. The opening is at our new state-of-the-art facility in Canton, MA. The successful candidate will engage in the Immuno Oncology research areas of the company and will work with a successful team of international senior scientists located in the USA and EU. The ideal candidate will have great communication skills, excellent technical skills, exemplary attention to detail, and a passion for learning. This position will have the opportunity to make significant scientific contributions to numerous drug discovery projects. | 01/21/2025 |
| 1822 | Pledge Therapeutics Canton, MA Research Associate, Virology Bachelor’s or Master’s degree in biological sciences or a related field Exp: 0-2 years |
We seek an enthusiastic and curious scientist interested in participating in all aspects of the hit-to-lead drug discovery process. The opening is at our state-of-the-art facility in Canton, MA. The successful candidate will engage in the company’s virology research areas and work with a successful team of scientists in the USA and EU. The ideal candidate will have great communication skills, excellent technical skills, exemplary attention to detail, and a passion for learning. This position will have the opportunity to make significant scientific contributions to numerous drug discovery projects. | 01/21/2025 |
| 1823 | PolyPeptide San Diego, CA Production Chemist BS degree in Chemistry or Biochemistry or equivalent Exp: 1+ years |
Checks reactor system for proper operation in accordance with SOP and/or operation manual. Under general supervision and direction, measures and mixes ingredients according to the BPR (Batch Production Record). Dispensing of raw materials from Pharmastore for Synthesis. During processing, monitors chemical reactions (color and completeness of chemical reactions) and under general direction of supervision and/or senior Production Chemist personnel responds with appropriate actions to ensure proper processing. Using established procedures (safety and process) and under general supervision, performs intermediate chemical processing steps. Prepares solutions for purification and samples. Under general supervision, purifies crude peptide by using HPLC’s. Conducts lyophilization process according to established guidelines. Performs drying processes in accordance with established processes and procedures. Reports any problems or issues regarding equipment used in processing to supervision and/or senior Production Chemist personnel. Performs in-process checking of the fractions by using analytical HPLC and reports results to supervision and/or Sr. Production Chemist personnel. Is responsible for maintaining high safety, housekeeping and cleanliness standards. Performs any and all additional duties as required for this position. | 01/21/2025 |
| 1824 | Polysciences Warrington, PA Quality Control Analyst I Bachelor’s degree in chemistry, chemical engineering or a similar field Exp: 1+ years |
We’re hiring a Quality Control Analyst in our Quality Control group who will use analytical equipment, analytical methods, and perform data analysis. Will test using GC, HPLC, LC/MS, KF, FTIR, UV-Vis, Viscometers, and Atomic Absorption, NMR, etc. | 01/21/2025 |
| 1825 | ProKidney Winston-Salem, NC Manufacturing Cell Processing Specialist 1 BS in Biotechnology, Biology, Chemistry, or related field; a Science-related discipline Exp: 0-2 years |
The Manufacturing Specialist, Cell Processing at ProKidney is responsible for supporting cell processing operations, ensuring compliance with cGMP guidelines in the development and production of regenerative medicine therapies. This role involves setting up and operating production equipment, including control rate freezers, orbital shakers, and other equipment, while contributing to efficient processing, freezing, and storage of cell therapy products. | 01/21/2025 |
| 1826 | ProKidney Winston-Salem, NC Cell Processing Specialist (Contractor) BS in Biotechnology, Biology, Chemistry, or related field; a Science-related discipline Exp: 0-2 years |
The Manufacturing Specialist, Cell Processing at ProKidney is responsible for supporting cell processing operations, ensuring compliance with cGMP guidelines in the development and production of regenerative medicine therapies. This role involves setting up and operating production equipment, including control rate freezers, orbital shakers, and other equipment, while contributing to efficient processing, freezing, and storage of cell therapy products. | 01/21/2025 |
| 1827 | ProKidney Winston-Salem, NC Manufacturing Support Specialist 1 BS in Biotechnology, Biology, Chemistry, or related field Exp: 0-2 years |
The Manufacturing Support Specialist I is essential in supporting manufacturing operations and maintaining the sterility and cleanliness of GMP facilities. This role involves aseptic processing of in-house solutions, media and kit preparation, GMP cleaning, and supporting manufacturing cell processing teams. The specialist is responsible for ensuring compliance with current Good Manufacturing Practices (cGMP), performing routine aseptic processing, preparing cleaning solutions for cleanroom sanitization, and ensuring proper documentation for biopsy and product shipments. This role also contributes to maintaining controlled environments, executing cleaning procedures, managing inventories, and collaborating with teams to improve manufacturing processes and cleanliness protocols. | 01/21/2025 |
| 1828 | Promis Dx Irvine, CA Laboratory Technician BS in Biology, Chemistry, or other medical-related sciences Exp: Entry level |
The Laboratory Assistant or Technician will follow the guidelines set by CLIA and the CA Business and Professional Code of Regulations (BPC: 1212 and 1269) for unlicensed laboratory personnel. | 01/21/2025 |
| 1829 | PsychoGenics Paramus, NJ Research/Data Analysis Assoc. Bachelor's degree in the biological scienes or related field Exp: 1-3 years |
We are looking for a highly motivated Researcher who can use, edit, and maintain our custom data processing software for our EEG group. The candidate must also work in a lab setting and will handle and work with rodents. The successful candidate will work in a team of scientists and researchers supporting preclinical studies using rodent models. The candidate must be capable of working both across teams and independently. The candidate will have support and training for the laboratory work from other EEG staff and will have support on the programming side from our Data Sciences team. The candidate will work with all senior staff in the EEG group and will work closely with the VP, Translational Neuroscience on developming the custom software to perform additional functions and analyses. | 01/21/2025 |
| 1830 | PTC Therapeutics Bridgewater, NJ Contract, Biology Master’s degree in a scientific discipline, preferably Biology, Biochemistry, or Neuroscience Exp: 0-1 years |
The Contract, Biology is responsible for performing scientific experiments that contribute to research and drug discovery activities at PTC. This position assists in the conduct of early-stage research, the goal of which is the identification of New Chemical Entities (NCEs), as well as the advancement of research programs from the identification of screening hits to advanced lead optimization. The incumbent is also responsible for communicating experimental results to his/her supervisor and the project team. The Contract, Biology supports adherence to all regulatory requirements and company Standard Operating Procedures (SOPs) including as appropriate. | 01/21/2025 |
| 1831 | Purolite Resins (EcoLab) Philadelphia, PA R&D Technical Analyst Bachelor’s degree Exp: 1 year |
Ecolab is looking for a R&D Technical Analyst who will perform a variety of routine tasks to maintain product specifications including mechanical or chemical characteristics of an item or product, who will work under minimal supervision and receive instruction only as necessary. The successful candidate will work on assignments and performs tasks that are moderately complex, where discretion is required in resolving problems and making routine recommendations regarding creation or maintenance of product specifications. | 01/21/2025 |
| 1832 | QIAGEN Germantown, MD Metrology Technician BS/BA Exp: 1-3 years |
The Metrology Technician performs equipment calibration assignments using standard methods and processes. Required duties include: Set-up, calibration, testing, repair, inspection and maintenance of equipment and tools. Making adjustments, modifications or replacements as needed. Maintain and document calibration of all measurement equipment (in the Electronic Calibration Maintenance Management System). Creating, maintaining, and updating department SOPs and other documentation as required. Coordinate the execution of the calibration program to include event scheduling, performance, and oversight of service suppliers. Provide notification of calibration tasks with due dates. Coordinate calibration scheduling with equipment owners when needed. Oversee work by outside calibration contractors to ensure compliance with applicable procedures. Troubleshoots and solves calibration and maintenance problems of moderate scope and complexity requiring broad technical interpretation of defined procedures and practices. Responsible for ensuring on-going compliance to applicable quality and EHS regulations and standards (e.g., cGMP, FDA, ISO, IVDD, OSHA, etc.). | 01/21/2025 |
| 1833 | Quality Agents Rockville, MA Quality Assurance Specialist BS in a technical discipline (Engineering, chemistry, microbiology, biology) Exp: 0-2 years |
Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. Our Quality Assurance Specialists are leading service providers to our clients providing GMP support. The individual will coordinate validation activities with the client and meet timelines. | 01/21/2025 |
| 1834 | Quality Agents Rockville, MA Validation Engineer I BS in a technical discipline (Engineering, chemistry, microbiology, biology) Exp: 0-2 years |
Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. Our Validation specialists will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The validation specialist will evaluate the equipment/utility/system/procedures used in development, production, and holding of pharmaceutical products and determine a validation approach. The individual should have experience with current US and international regulations, guidance, industry best practice in one of the following areas of validation: facilities, utilities, and equipment qualifications, process validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the validation specialist must be approved by the client. | 01/21/2025 |
| 1835 | QuidelOrtho Rochester, NY V&V Engineer I (R&D) B.S. Degree in Computer Science, Chemistry, Biochemistry, Biology, Engineering, or a related discipline Exp: 1-2 years |
As QuidelOrtho continues to grow, we are seeking a Verification and Validation Engineer I to help with formal verification and validation of complex medical devices under the regulations of the FDA. The individual will be part of an engineering team that is responsible for requirements based test design and execution of test procedures both in a virtual and lab environment. The team is highly collaborative and will require regular interactions in formal reviews, test planning activities, and working with software development to reproduce and verify system defects. | 01/21/2025 |
| 1836 | QuidelOrtho Carlsbad, CA Quality Engineer B.S. Degree in Chemistry, Biochemistry, Biology, Engineering, or a related discipline Exp: 1+ years |
As we continue to grow as QuidelOrtho, we are seeking a Quality Engineer. This position is responsible for owning and coordinating all Quality Engineering functions and activities for the defined processes. This individual is also responsible for supporting the Production, Quality Control, Engineering and Quality Assurance departments and the associated activities, which include receiving inspection, in-process inspection, and finished goods inspection in achieving and exceeding company goals and objectives. In addition, this individual is responsible for supporting the administration, implementation, and continuous improvement of the quality systems associated with non-conforming materials, inspection control plans, and corrective/preventive action. This individual also supports corporate strategic goals and objectives through internal audits, support of manufacturing operations, quality support for manufacturing processes for new product development/ product improvement projects, and support of manufacturing process improvement projects. | 01/21/2025 |
| 1837 | QuidelOrtho Athens, OH Associate Biochemist Bachelor’s Degree in a biology, biochemistry, chemistry or other related science field Exp: 1 year |
The Associate Biochemist is responsible for the production and quality testing of various raw material, intermediate components and finished good catalog items, in accordance with Quidel’s Quality System Regulations. | 01/21/2025 |
| 1838 | QuidelOrtho Raritan, NJ Facilities Engineer BS in Engineering Exp: 1-2 years |
As the company continues to grow, we are seeking a Facilities Engineer to provide support of the facility equipment and supporting systems to efficiently maintain and reliably operate the site. The position will provide support of maintenance staffing services, assessment and control of performance metrics, and attainment of cost objectives in daily maintenance and operation of all facility assets. Supporting systems include maintenance work management, building control, quality, procurement, training, and all associated supporting procedures. Position is to continuously assess general condition and readiness of critical assets required to deliver business priorities without interruption. Position has overall responsibility for all infrastructure and staffing capability to ensure reliable and efficient facility operations. Deliver high quality, safe, compliant, cost effective facilities infrastructure. | 01/21/2025 |
| 1839 | Quintara Discovery Hayward, CA Senior Research Associate Master’s degree in Biology or related field. Exp: 1 year |
Responsible for exercising independent judgment in conducting research on in vitro ADME screening (ADME: Absorption, Distribution, Metabolism, and Elimination): plan experimental approaches; design and carry out bioanalytical tests of various compounds for the potential development of human therapeutics; analyze and interpret experimental data and prepare reports of findings. Design and perform procedures in ADME assay projects by operating lab equipment, including integrated hardware, software, optical and fluidic subsystems. Conduct sample bioanalysis and develop bioanalytical methods for the quantitative analysis by using mass spectrometry. Document information on procedures, modifications, and methods; maintain records of experiments and results in the accessible format. | 01/21/2025 |
| 1840 | Quotient Sciences Boothwyn, PA Validation Engineer BS Degree in Engineering Exp: 1-3 years |
This role will Provide engineering support for maintenance and validation activities. Maintain engineering documentation and support the completion and maintenance of both equipment impact and instrument assessments. Whilst complying & adhering to Good Manufacturing Practice (GMP) standards. | 01/21/2025 |
| 1841 | Quotient Sciences Garnet Valley, PA QC Scientist II Master’s degree in Chemistry or other related field of study Exp: 1+ years |
We have a full-time position available for an QC Scientist II at Quotient Sciences Philadelphia site in Garnet Valley. The QC Scientist II is responsible for analytical release and stability testing under the supervision of the Group Leader within the Clinical Quality Control Team. You will join a supportive team of experienced QC Analysts and perform the following duties. | 01/21/2025 |
| 1842 | Quotient Sciences Garnet Valley, PA Manufacturing Scientist B.S. Degree in Chemical Engineering, Pharmacy/Pharmaceutical Sciences or other related field Exp: Entry level |
Conduct lab work as planned by the supervisor that involves development of pharmaceutical formulations such as tablets, capsules, and liquids. Conduct pharmaceutical manufacturing of oral dosage forms using small to large-scale equipment for development and process scale-up and for clinical supplies. Review and write master batch records with input from the supervisor. Prepare executed batch record folders. Comply with cGMPs, SOPs, and Company policies. Operate manufacturing equipment with the Operator for development clinical manufacturing. Maintain a planned training schedule and record. Completion of clinical batch manufacturing as per timeline. Ability to perform physical work while using a respirator. Read and interpret documents such as batch records, SOPs, policies, and safety rules; read and write business correspondence. Define problems, collect data, establish facts, and draw valid conclusions. Interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. Basic knowledge of physicochemical concepts and theories. Familiarity with the production process. Familiar with a variety of in-process equipment, such as disintegration, friability, particle size, etc. | 01/21/2025 |
| 1843 | Raybow Brevard, NC Synthetic Organic Chemist B.S. or M.S in Organic Chemistry Exp: 0-4 years |
Preferred candidates have work experience in multi-step synthesis of small molecules and should be able to design and develop practical synthetic routes to target compounds. A strong organic chemistry background with the ability to plan and execute complex syntheses is required. Successful candidates must have good verbal and written skills for communicating with management and clients. Excellent opportunity at all levels for growth and advancement. | 01/21/2025 |
| 1844 | Raybow Brevard, NC Analytical Chemist - Pharmaceutical B.S. or M.S in Organic Chemistry Exp: 0-4 years |
Preferred candidates have work experience in multi-step synthesis of small molecules and should be able to design and develop practical synthetic routes to target compounds. A strong organic chemistry background with the ability to plan and execute complex syntheses is required. Successful candidates must have good verbal and written skills for communicating with management and clients. Excellent opportunity at all levels for growth and advancement. | 01/21/2025 |
| 1845 | RayzeBio (Bristol Myers Squibb) San Diego, CA Associate Scientist, Chemistry BS or MS in Chemistry or related field Exp: 1-5 years |
RayzeBio is looking for an Associate Scientist to support in the development of novel therapeutics in preclinical stages. Candidates will work as part of a team of scientists to synthesize and design both small molecules and peptide analogs to optimize potency, pharmacokinetics, and in vivo efficacy of potential drug candidates. This position offers a challenging and rewarding work environment within a thriving company. | 01/21/2025 |
| 1846 | Reckitt Wanamingo, MN Compliance Assurance Lead/Associate Bachelor’s Degree in technical discipline (science/ engineering/ food processing, etc) Exp: 0-2+ years |
Manages and monitors site quality performance reporting requirements including root cause analysis, corrective action, and implementation to ensure compliance to QMS. Perform or review manufacturing non-conformance reports, CAPA, failure investigations, and audit findings to report manufacturing-related issues that may impact quality and recommend courses of corrective action. Prepare and analyze metrics for EM, CAPA, and suppliers’ performance to drive continuous improvement. Interface with suppliers to ensure the product meets specifications. Ensure compliance with all procedures for batch release. Develop knowledge of QC testing programs and capabilities. Assist in securing information for investigation, root cause, preventative action, and closure of non-conformities. Assist in the design and execution of validation protocols when required. Assist in the development and implementation of quality and productivity improvement projects. Perform HACCP GMP, Reckitt Nutrition Standards verification, and other quality and compliance audits as required. Ensure updates are made to the HACCP and Food Safety Plans based on the impact of changes in the plant from a Hazard Assessment and Risk-Based approach. Drive continuous improvement activities on the production line with training, SOP updates, etc. Other duties may be assigned. | 01/21/2025 |
| 1847 | Ofni Systems Raleigh, NC Computer Systems Validation Engineer BS or equivalent degree in math, science or engineering Exp: 1 year |
We are hiring a Validation Engineer to be on the cutting edge of automated validation techniques. You will be responsible for implementing our validation solutions while working with industry-leading companies. Ideal candidates are experts on the requirements of 21 CFR 11, have excellent critical thinking and interpersonal skills, and are motivated to meet client needs for compliance. If you are an A-level engineer who enjoys the challenge of solving real-world compliance problems then we would like to talk with you. | 01/16/2025 |
| 1848 | Olympus Brooklyn Park, MN Manufacturing Engineer II Master's degree in Engineering or Physics, or a related field Exp: 0+ years |
The position holder is responsible for the execution and documentation of process development deliverables and activities for Single Use Endoscopes (SUE) product development and launch to production. The position holder implements the optimal manufacturing processes according to product delivery, operations, and business requirements to launch products effectively, on time, with high reliability and the right cost. The position holder responsible for proactive engineering responses in alignment with Regulatory compliance requirements. | 01/16/2025 |
| 1849 | Olympus San Jose, CA Repair Engineer I Bachelor's Degree in Engineering Exp: 1 year |
Provide engineering support for introduction of new products and alternate repair activities. Function as Project Coordinator on more complicated projects as defined by the Manager by providing technical information to other project participants recommending cost effective procedures tracking and maintaining implementation dates and documenting completed projects. Provide support to Associate Engineer on his/her assigned projects. | 01/16/2025 |
| 1850 | Olympus Brooklyn Park, MN Manufacturing Engineer II Bachelor’s degree (B.S.) in science/engineering discipline or equivalent industry Exp: 0-2 years |
The Manufacturing Engineer-I will assist in supporting the day to day operation of the value stream or perform process development activities. They will strive to optimize processes for manufacture and product flow including down time mitigation, root cause investigations and cost savings initiatives. | 01/16/2025 |
| 1851 | Olympus Memphis, TN Repair Engineer I Bachelor's degree in engineering Exp: 1 year |
Provide engineering support for introduction of new products and alternate repair activities. Function as Project Coordinator on more complicated projects as defined by the Manager by providing technical information to other project participants recommending cost effective procedures tracking and maintaining implementation dates and documenting completed projects. Provide support to Associate Engineer on their assigned projects. | 01/16/2025 |
| 1852 | Olympus Brooklyn Park, MN R&D Engineer II Master’s degree in engineering (Biomedical or equivalent preferred) Exp: 0 years |
The Engineer II on the Sustaining Engineering team is responsible for supporting all aspects of Sustaining Engineering efforts, including supporting project definition activities, leading/supporting verification and validation efforts, and overseeing implementation. In particular, it will be the responsibility of the Engineer II to advance technical efforts, while proactively identifying potential issues, to achieve a timely launch of high quality / reliable product. He or she must have a working knowledge medical device design control requirement, be able to technically contribute to the project team, and work collaboratively across the organization to ensure an effective implementation of the improvement, solution, or line extension. As the Engineer II will contribute to Design History Files, maintaining detailed documentation throughout all phases of the project is essential. | 01/16/2025 |
| 1853 | OncoC4 Rockville, MD In-house CRA Bachelor’s degree in Sciences with strong emphasis in science and/or biology Exp: 1 year |
In house Clinical Research Associate (In-house CRA) will act as the clinical operations person to participate in IRB and TMF document submissions related to site selection, activation, maintenance, and closeout activities, in site monitoring and compliance management, and data integrity monitoring functions within OncoC4, supporting ongoing and future OncoC4 clinical trials of novel immune therapies for cancers. | 01/16/2025 |
| 1854 | OncoPep Cambridge, MA Research Associate (In Vitro) BS Exp: 1 year |
We are looking to expand our Research team by recruiting a skilled Research Associate in cellular/molecular biology to join our growing team. The candidate will primarily work with molecular and cell biology techniques including culture of primary cells and cell lines, flow cytometry, ELISA, and western blot. He/She will play an important role in the discovery and development of novel biotherapeutics for immuno-oncology. He/she will be responsible for generating the tools necessary for evaluation and screening of lead candidate therapeutics. He/she will be expected to participate in experimental design, conduct experiments, optimize throughput, maintain detailed records, and generate standard operating procedures. | 01/16/2025 |
| 1855 | Orchid Santa Ana, CA Quality Engineer Bachelor of Science (B.S) Exp: No exp |
The Quality Engineer I supports the ongoing quality of Orchid's legacy products & processes and works cross-functionally to sustain the business. | 01/16/2025 |
| 1856 | OrganaBio Miami, FL Cell Processing Associate Bachelor or Associate Degree in Biology, Cell and Molecular Biology, Biotechnology, Biomedical Engineering, or related field. Exp: 1-2 years |
This is a temporary role that has the possibility to convert to full time employment at the end of 90 days. A Cell Processing Associate assists in the performance of primary peripheral blood mononuclear cells (PBMCs) isolation from patient samples, as part of screening efforts for various customers. This position will help contribute to PBMC isolation process improvement, to drive efficiency in the documentation and production process. This role will support Process Development (PD) team efforts, and interact cross-functionally with teams that include, but are not limited to Business Development and Quality Assurance, to ensure company milestones are met. This position will ensure that products are processed under GLP practices, with appropriate documentation in place, it will also interact with external customers for which samples are processed, assuring that such communication is clear and disseminated in time, and processed samples are shipped back to customer, according to customer timeline. | 01/16/2025 |
| 1857 | Organogenesis Norwood, MA QC Analyst I-Cell Culture Bachelor’s degree in biology or related field Exp: 1-3 years |
The QC Analyst I, Cell Culture performs quality activities in support of product production and release for ASA Product. This position interacts with other internal departments, including Production, Quality Assurance, Validation, Calibration, Materials, and Logistics. The position also interacts with external entities including contractors and suppliers. The QC Analyst I performs a variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending, and reporting results. | 01/16/2025 |
| 1858 | Organogenesis Norwood, MA QC Analyst I - Chemistry Bachelor’s degree in biology or related field Exp: 1-3 years |
The QC Analyst I, Chemistry performs quality activities in support of product production and release for ASA Product. This position interacts with other internal departments, including Production, Quality Assurance, Validation, Calibration, Materials, and Logistics. The position also interacts with external entities including contractors and suppliers. Performs a variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending, and reporting results. | 01/16/2025 |
| 1859 | Orthofix Lewisville, TX Associate Quality Engineer - Operations B.S. Engineering degree or equivalent Exp: 0-2 years |
The Associate Quality Engineer engages with cross-functional team members and suppliers to drive Quality performance and to ensure that product quality meets all internal and external requirements. They will support initiatives to improve quality and customer satisfaction. The Associate Quality Engineer position also ensures compliance with Quality system and other standards and regulations, company quality requirements and corporate objectives. | 01/16/2025 |
| 1860 | Orthofix Carlsbad, CA Clinical Lab Associate Bachelor’s Degree Exp: 1 year |
Orthofix is looking for a Clinical Lab Associate (CLA) to join our team at our corporate headquarters in Lewisville, TX. As the Clinical Lab Associate you will be responsible for the successful execution and lab planning for all spine courses, HCP training, and internal stakeholder training. This includes working with Medical Education teammates, Marketing, R&D, Regulatory, and Compliance departments to facilitate hands-on surgical training and execute courses and given projects that are set forth by the Spine management. This position includes the utilization of equipment including audiovisual processes, inventory of lab supplies, (add “surgical) instruments, cadaveric specimens, and demo set shipments to the field and Spine office locations. In this role you will work daily with the Medical Education Events Team to coordinate and exceed lab attendees’ overall experience and expectations. This position is responsible for holding the Company, mission and objectives as guiding business principles, remaining in compliance with all safety and HCP protocols, and for driving constant and consistent quality improvement and industry best-practices. | 01/16/2025 |
| 1861 | DPT Laboratories (Viatris) San Antonio, TX Associate Scientist Q Bachelor’s degree in Life Science Exp: 0-2 years |
Testing of chemical components or products. Will involve the use of major laboratory instruments and equipment: HPLC, GC, FTIR, UV/VIS, as well as utilizing wet chemicals skills. Analytical review of data to ensure calculations is complete and accurate. Performs quantitative chemical analyses of APIs and related materials under direct supervision following established procedures and guidelines using laboratory instrumentation such as gas chromatographs, liquid chromatographs, ultraviolet-visible spectrophotometers, etc. Performs microbiological analysis as required. Treats numerical data throughout chemical analysis by performing mathematical calculations such as determining concentrations (molarity, parts per million, normality, etc.) and statistical information (standard deviation, mean, etc.). Prepares necessary reagents and equipment to expedite the performance of analysis by measuring and/or weighing chemicals, missing, and standardizing solutions, and assembling equipment. Maintains accurate records by logging samples received, recording samples analyzed, procedures used, and results obtained on datasheets and/or laboratory notebook. Weights and calculates samples in the physical and chemical analysis of products using balances and measured volumetric containers. Recognizes and informs Group Leader about daily lab activity and analytical problems. Organizes and properly labels samples, sample preparations, volumetric solutions etc. Perform other duties as assigned. | 01/16/2025 |
| 1862 | Mylan Pharmaceuticals (Viatris) Greensboro, NC Maintenance Technician Bachelor’s degree Exp: 1-2 years |
Perform daily and weekly tests of and coordinate maintenance on all facility life safety and fire suppression equipment, power and alternative power sources, interior and exterior light sources, and PIT equipment. Perform general painting and maintenance of warehouse interior and exterior, including but not limited to installation and repair of door hardware, drywall repair, storage rack repair or replacement, replacement of ceiling or carpet tiles, welding/grinding, plumbing fixture installation or replacement and light construction projects. Monitor and assist HVAC, refrigeration, fire protection, and fire alarm vendors and contractors when maintenance or repairs are being performed on equipment. Assemble and install furniture, furnishings, artwork, etc. as needed in the office and warehouse areas. Initiate, complete or file Trackwise Events and documentation as required. Issue, document and record Hot Work and Red Tag permits including coordination and communication with local emergency services providers during Red Tag events. Issue, document and record Lockout/Tag out events. Document and file Mylan Insurance Provider and Mylan EH&S department required records for NFPA inspections, life safety equipment and NCDENR required logs for property maintenance. | 01/16/2025 |
| 1863 | Mylan Pharmaceuticals (Viatris) Greensboro, NC Quality Technician, Inspections Bachelor’s degree Exp: 0-2 years |
Perform physical counts of outsourced products received. Prioritize and perform attribute inspections of outsourced products. Process product requisitions. Process returned goods and assign disposition. Create and maintain product specifications for outsourced products. Accurately compare product specifications with product. Process Notice of Rejections and TrackWise records for damaged products and returned goods. Collect temperature data for temperature monitored shipments. Operate forklift or related warehouse equipment as needed to perform job. Maintain and report departmental metrics. | 01/16/2025 |
| 1864 | Pacific BioLabs Hercules, CA Microbiology Laboratory Analyst II/III - Senior Analyst MS in Biology, Pharmaceutical Sciences, Biotechnology or equivalent - Microbiology degree preferred Exp: 1+ years |
PBL has an immediate opening for a fulltime onsite Microbiology Laboratory Analyst II/III or Senior Analyst, depending on experience, in the Microbiology Services Department. The Microbiology Laboratory Analyst II/III or Senior Analyst will report to the Director of Microbiology and will contribute to general and complex laboratory testing, sample management and laboratory maintenance. The Microbiology Laboratory Analyst or Senior Analyst is expected to participate with the team to meet Microbiology Services Department goals and perform routine and non-routine laboratory duties as directed. As a member of the PBL Microbiology Services team, the Analyst will make contributions to the growth of the department primarily through laboratory testing, training peers, validations, and support of the company’s continuous improvement initiatives and client needs. This position is client-facing, and the analyst must be quality focused and work in accordance with the PBL Quality Management System. | 01/16/2025 |
| 1865 | Pacific BioLabs Hercules, CA In Vitro Research Assistant I/II/III Bachelor’s Degree in a science-related field (e.g., Biological Sciences, Toxicology, Pharmacology) Exp: 1-3 years |
PBL has immediate openings for a Research Assistant I/II/III in the In Vitro Services Department. The Research Assistant reports to the Director, In Vitro Services. The In Vitro Research Assistant is a laboratory level job focusing on the development, optimization, and execution of a variety in vitro (i.e., cell-based and noncell-based) test methods. Successful candidates will be familiar with laboratory procedures including the use of analytical balances, calculating, and preparing dilutions, pipetting, measuring pH, documenting study activities, and analyzing/interpreting data. The In Vitro Research Assistant is expected to perform under minimal supervision. Research Assistants may also contribute to general laboratory operations including equipment maintenance and maintaining a clean and organized laboratory environment. | 01/16/2025 |
| 1866 | PacBio Menlo Park, CA Scientist I, Reagent Quality Control Master’s in a scientific discipline Exp: 1-2 years |
PacBio is seeking a driven, self-starter for the position of Reagent Quality Control (QC) Scientist. In this role, the QC Scientist is required to complete high quality work through QC assay execution from analytical assays (e.g., HPLC, fluorescent assays, etc.) to Use Test assays involving PacBio’s sequencing platforms. In addition, the individual will complete QC assay validation and transfer activities, execute stability studies, trend and interpret data, troubleshoot QC failures, and complete sustaining QC process improvements in the Reagent Manufacturing Organization. In this multi-faceted role, the ideal candidate is organized, independent, detailed oriented, process driven, quality driven, and skilled at problem solving. | 01/16/2025 |
| 1867 | Pacific Edge Diagnostics Hummelstown, PA Laboratory Technician Bachelor's degree in medical technology, chemical, physical, or biological sciences Exp: 1 year |
Pacific Edge Diagnostics USA, an innovative cancer detection testing company is seeking a talented Clinical Laboratory Technician to join its team. The Clinical Laboratory Technician's primary responsibility will be to perform molecular clinical testing (from specimen receipt through reporting patient results), as well as general lab maintenance. | 01/16/2025 |
| 1868 | Pall (Danaher) Cortland, NY Engineer I Bachelor of Science in Engineering required. Mechanical, Chemical, Materials or Industrial Engineering Exp: 1+ years |
In the role of Engineer I, you will have the opportunity to apply your skills in project management, research and principles of engineering to the planning, design, development, documentation, and testing/debugging of a variety of materials, components & finished goods in context of change management resulting from supplier obsolescence. his position is an onsite position and is located in Cortland, NY. | 01/16/2025 |
| 1869 | Pandorum Technologies San Carlos, CA Associate Research Scientist Master’s Degree in Life Sciences and related discipline Exp: 1 year |
Perform biochemical and cell-based assays, assay development, protein production and characterization, ELISA, western, biomarker studies and use various molecular biology tools. Work with a team of scientists towards establishing various protocols with high quality, generate reproducible SOPs compatible with cGMP process for technology/knowledge transfer for clinical grade production. Develop and optimize protocols for various cell and molecular biology studies, such as RNA preparation and RT-PCR. Protein production, purification, characterization and analysis by ELISA, SDS-PAGE, western, other biochemical techniques. Generate data for Company newsletter, website, social media, printed journals etc. Analyse data and prepare reports. Prepare SOPs for various experimental procedures. Prepare data for internal and external presentations, communications and publications. Participate in team meetings and scientific discussions | 01/16/2025 |
| 1870 | Paragon 28’ Englewood, CO Associate Product Sustaining Engineer Bachelor’s degree in Mechanical Engineering, Biomedical Engineering or related engineering discipline Exp: 0-3 years |
The Associate Product Sustaining Engineer works with direction from senior Engineering staff on projects that focus on legacy product systems and design and development of medical devices. | 01/16/2025 |
| 1871 | Paragonix Technologies Waltham, MA Associate Quality Engineer - Operations Bachelor’s Degree in an engineering or scientific discipline. Exp: 1 year |
As an Associate Quality Engineer, you will work closely with cross-functional teams to support various aspects of quality engineering, with a focus on New Product Introduction and failure analysis. Reporting to the Manager, Quality Engineering, you will assist in implementing and maintaining quality systems and processes to meet regulatory requirements and industry standards. | 01/16/2025 |
| 1872 | Paragonix Technologies Waltham, MA Quality Engineer Bachelor’s Degree in an engineering or scientific discipline. Exp: 1-3 years |
The Quality Engineer plays an integral role in Paragonix’s Quality Department as a hands-on engineering role conducting post market investigations of FDA approved medical devices. The position requires strong organization skills, attention to detail, ability to work in cross functional teams, and drive to accomplish departmental and company goals. | 01/16/2025 |
| 1873 | PCI Bedford, NH QC Microbiologist I BS/BA degree in Microbiology or related scientific field. Exp: 1 year |
The Microbiologist I conducts sampling and testing of production environments, and/or facility clean utilities, as per approved procedures. Performs Lab work and other tasks as assigned by management. | 01/16/2025 |
| 1874 | PCI Madison, WI Validation Engineer I Bachelor’s degree in Engineering or related scientific discipline Exp: 1-3 years |
The Validation Engineer I performs an array of well-defined validation activities in support of cGMP pharmaceutical/medical device contract manufacturing across multiple PCI facilities. In collaboration with validation management, the Engineer I assist with internal project teams and external validation firms on validation/qualification initiatives and ensures project schedules are met. Complies with requirements of the Safety Program, including PCI Health and Safety mandates and OSHA requirements. In carrying out duties, contributes and promotes a positive and equitable working environment emphasizing the PCI Values: Customer Focus, Innovation, Integrity, Collaboration, and Superior Performance. | 01/16/2025 |
| 1875 | PCI Rockford, IL Operations Process Engineer Bachelor's Degree in a related field Exp: 1-5 years |
This position will work to continuously improve processes and systems that ultimately lead to improved profitability to the company. Using all available Engineering, Lean, and Six Sigma tools, this position will work independently and cross-functionally to drive out waste and reduce process variability. | 01/16/2025 |
| 1876 | PCI Rockford, IL RFD Microbiologist 1 Bachelor's Degree in a related field Exp: 1-5 years |
The primary function of this role is to perform basic tasks such as collect and process environmental samples from across all Rockford facilities using aseptic technique. In addition, this role is responsible for supporting basic microbiological functions and daily monitoring of the Laboratory temperature for various equipment in the Laboratory. This role may participate in training of other analysis in techniques for which competency has been demonstrated. There are no supervisory responsibilities associated with this role. | 01/16/2025 |
| 1877 | Penumbra Alameda, CA Manufacturing Engineer II, Operations Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering or related degree Exp: 1+ years |
The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and that support continuous improvement in production. Project opportunities are designed to develop professional work knowledge and abilities and to support the efforts and projects that have global importance to the success of the business. Area of work involves manufacturing and business processes with interaction between production, cross-departmental engineering groups, and other cross-functional teams (such as Regulatory, Quality, R&D, Supply Chain, IT, etc.) in executing and coordinating business operations systems projects and activities. Essential job functions include creating and executing an integrated cross-functional project plan. | 01/16/2025 |
| 1878 | Penumbra Alameda, CA Quality Monitoring & Improvement Specialist I Bachelor's degree preferably in engineering, life sciences, or a related field Exp: 1+ years |
As a key member of the Quality team, you will have a hand in ensuring that Penumbra's life-saving products adhere to the highest standards of quality and safety. In the Quality Monitoring & Improvement Specialist I role, you will be supporting our Quality Management System (QMS) processes, specifically Corrective and Preventive Actions (CAPAs), Nonconformance Reports (NCRs) and Deviation Authorizations (DAs) following Penumbra's procedures and regulatory requirements. You will organize and host board meetings to facilitate board review of documentation supporting these systems. You will also assist with data compilation for monthly trending meetings. | 01/16/2025 |
| 1879 | LabCorp Phoenix, AZ Molecular Technologist Bachelor’s degree in Chemical or Biological science, Clinical Laboratory Science, Medical Technology Exp: 1 year |
Are you an experienced Clinical Lab Professional? If so, Labcorp wants to speak with you about exciting opportunities to join our team as a Technologist at the Sunshine Lab in Phoenix, AZ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at Labcorp: “Improving Health, Improving Lives”. | 01/16/2025 |
| 1880 | LabCorp San Antonio, TX Lab Technologist - Molecular Microbiology Bachelor’s degree in Chemical or Biological science, Clinical Laboratory Science, Medical Technology Exp: 1 year |
Are you an experienced Clinical Lab Professional? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist at in San Antonio, TX. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. | 01/16/2025 |
| 1881 | LabCorp Saint Paul, MN MCT Laboratory Technologist Trainee Bachelor's degree in chemical, biological or clinical laboratory science or medical technology. Exp: No exp |
Are you looking to embark on a new challenge? The possibilities are endless when start your career at Labcorp! We would love to discuss the exciting opportunities you will encounter when you join our team as a Technologist Trainee. In this position, you will work in a patient focused, fast paced, and inspiring environment. You will have a dynamic role in the fulfilment of Labcorp’s overall mission of “Improving Health, Improving Lives.” The MCT Department is looking for a Technologist Trainee to work in our laboratory. The candidate will receive on-the-job training for the pre-analytical through post-analytical set-up and testing of patient samples. This laboratory is responsible for screening blood, serum, urine and meconium sample types for drugs of abuse. We also perform Therapeutic Drug Monitoring (TDM) and STAT testing for local clinics and hospitals. The MCT Laboratory uses immunoassay methodology (Beckman Coulter AU5800 Chemistry analyzers) to test samples. Some assays require a chemical extraction before analysis. | 01/16/2025 |
| 1882 | LabCorp Madison, WI Research Assistant Bioanalytical -LCMS Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field Exp: 1+ years |
Do you have a strong background in LCMS? Are you wanting to apply your LCMS skills into improving the lives and wellness of people around the globe? Join Labcorp Biopharma as a Research Assistant in our Bioanalytical Metabolism Team in Madison, WI. Put your background with LC-MS Liquid chromatography and Mass Spectrometry focusing on large molecule sample analysis. We’re looking for a flexible, research and development focused individual who can think outside the box and is interested in bioanalysis of liquid and tissue matrices. As a Research Assistant in our Bioanalytical team you will provide assistance with experiments and with analytical and routine scientific procedures according to protocols. | 01/16/2025 |
| 1883 | LabCorp Madison, WI Lab Scientist Bachelor's degree in biology, chemistry, or related life science Exp: 1-2 years |
Labcorp Drug Development, the world’s most comprehensive drug development company, dedicated to improving healthcare and improving lives. Our unique perspectives, built from decades of scientific expertise and precision delivery of the largest volume of drug development data in the world, along with our innovative technology solutions, help our clients identify new approaches and anticipate tomorrow’s challenges as they evolve. We are looking for the right candidate to join our team in Madison, WI as a Lab Scientist! Come and be a part of helping many and fulfilling Labcorp's mission of improving health and improving lives! | 01/16/2025 |
| 1884 | LabCorp Greenfield, IN Sample Processing Technician Bachelor’s degree in Life Sciences such as Animal Science, Biology, Chemistry, Wildlife Studies or related field Exp: 1+ years |
Lab Sampling Technician-Study Tech position in our Greenfield IN location is responsible for the timely and accurate receipt, processing and storage of laboratory samples in compliance with GLP guidelines, study protocols and standard operating procedure, as well as managing the inventory of biological samples. | 01/16/2025 |
| 1885 | LabCorp Greenfield, IN Research Assistant (Study Tech) Animal Operations achelor’s Degree in Animal Science, Biology, Wildlife Studies, or related life science field Exp: 1-2 years |
Your work will contribute to improving the lives and wellness of both people and animals around the world. In this position you will be conducting Animal Research studies that will be looking at the safety, effectiveness and toxicity of drugs that are in early development phase and/or chemical substances. You’ll be maintaining the highest standards of animal care and welfare in accordance with Association for Assessment and Accreditation of Laboratory Animal Care International (AAALAC). Some of the most common tasks include performing various dosing techniques, may perform bleeding techniques, may collect biological samples, basic measurements such as body weight, food consumption, body temperature, blood pressure, etc. In this position your work will play a key role in bringing new scientific discoveries to life and make a difference in the lives of millions! | 01/16/2025 |
| 1886 | Pfizer McPherson, KS Process Engineer - Capital Engineering Bachelor's degree Exp: 0+ years |
The Capital Engineering Process Engineer is a key technical role responsible for providing engineering and process equipment expertise for the execution of Capital projects at the McPherson site. The role requires a high level of technical expertise in pharmaceutical processing systems, formulation equipment, high purity piping distribution systems, aseptic filling operations, terminal sterilization processes, inspection / packaging equipment, and clean room facilities design requirements. The incumbent will provide focused process ownership and the technical expertise to ensure high quality and efficient sterile injectable products. As technical lead, the Capital Engineering Process Engineer partners with supervision and production colleagues to identify and implement innovative solutions. This role focuses on developing new processes on site, resolving engineering issues, and providing technical support and troubleshooting during all phases of the Capital project. The Capital Engineering Process Engineer supports the Capital Portfolio Manager in the execution of assigned projects, which may include the coordination of internal company resources and vendors as part of the execution of projects. | 01/16/2025 |
| 1887 | NAMSA Irvine, CA Senior Laboratory Technician - Quality Control Bachelors degree Exp: 0 years |
May perform various testing independently in accordance with SOPs and utilizing applicable work instructions, standards or guidelines. Performs routine calculations and may participate in analyzing and interpreting results. Maintain all test equipment and supplies for various testing. Clean glassware and prepare reagents for use in laboratory testing. Perform routine disposal of laboratory waste including disposal of test articles. Assist with making solutions and preparing reagents.Assist in the preparation of items for testing. Monitor raw materials and final finished media for conformance with applicable material specifications and SOPs. May be responsible for extractions, which may include: test article and control preparation, animal holding and preparation and solution preparation. May be responsible for chain of custody, delivery of samples, filing and sample distribution/shipping. Accurately collect and record raw data in logbooks and on worksheets. Maintain clean workspace, testing supplies, and equipment. May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable and in accordance with criteria outlined in Standard Operating Procedures. May be required to operate specified laboratory equipment as applicable. Maintains an efficient workflow process relative to sample prioritization. Other duties as assigned. | 01/06/2025 |
| 1888 | Nanomix San Leandro, CA Associate Scientist, Assay Development Bachelor’s degree (or equivalent) in in Biology, Bioengineering, Chemistry, Chemical Engineering, or related field Exp: 0-2 years |
Nanomix has developed tests for the diagnosis of sepsis, acute kidney injury, and COVID-19, and is looking for an Assay Development Associate Scientist to help accelerate these programs and the development of other IVD assay products in the pipeline. This is an opportunity to work with a world class team to deliver an advanced, mobile medical diagnostic platform of urgent need to the healthcare industry. | 01/06/2025 |
| 1889 | NantWorks Culver City, CA Battery Technician Bachelor’s in a technical field Exp: 0-3+ years |
The Battery Technician is a key position within Research & Development that assists in building test cells to guide decision-making. They will be responsible for approaching cell engineering and fabrication with a high level of detail and integrity. The ideal candidate would be extremely flexible, curious, resilient, and eager to learn. | 01/06/2025 |
| 1890 | Natera Austin, TX Clinical Laboratory Operator Extractions BS/BA in a biological science or a related field Exp: 0-2 years |
This position assists in analyzing specimens and maintaining equipment in good operating condition to ensure accurate and timely testing of patient samples. This role involves adhering to Good Laboratory Practices (GLP), troubleshooting equipment malfunctions, providing guidance to new team members, and maintaining compliance with regulatory standards. The technician plays a crucial role in supporting laboratory operations, ensuring a clean and organized workspace, and contributing to continuous improvement initiatives. | 01/06/2025 |
| 1891 | Natera Austin, TX CQV Engineer II BS/BA in a biological science/biomedical engineering, similar field of study Exp: 1 year |
We are seeking a Commission, Qualification and Validation (CQV) Engineer II to support the commissioning and validation of laboratory and robotic equipment. The ideal candidate will have hands-on experience in writing and executing IQ, OQ, and PQ protocols to ensure compliance with regulatory and quality standards. | 01/06/2025 |
| 1892 | Natera Austin, TX Instrument Support Engr 2 BS/BA in a biological science/biomedical engineering, similar field of study Exp: 1-3 years |
The Instrument Support Engineer is responsible for the service and support of laboratory equipment and instrumentation utilized in the Operations laboratory. The scope of support includes installation, calibration, maintenance, and repair of both simple (e.g., plate sealers) and complex (e.g., liquid handling robotics) instrumentation in the laboratory. The Instrument Service Engineer will be the primary point of contact for production lab personnel when equipment and instruments are not operating or not meeting operational specifications. | 01/06/2025 |
| 1893 | LGC Remote/Alexandria, MN Field Application Scientist I Bachelor's or Master's degree in Molecular Biology, Biochemistry, Chemistry, Genetics, or related field required. Exp: 1-3 years |
The Field Service Application Scientist I is a multi-disciplinary molecular biology and organic chemistry position that will contribute to the organization as part of our Global Field Service team, bringing curiosity, problem solving skills, and scientific acumen to LGC. The Field Service team supports various wings of the organization such as Laboratory Operations, Engineering, Sales, and Manufacturing. | 01/06/2025 |
| 1894 | LGC Cumberland Foreside, ME Quality Control Technologist I Bachelor’s degree in Medical Technology (preferred) or related science degree (i.e. biology, chemistry, biochemistry) Exp: 1-3 years |
Follows standardized procedures and prepares samples for testing. Analyzes test results for accuracy, acceptability, and critical limits. Relies on limited independent judgment to plan and accomplish goals. Performs a variety of tasks. A limited degree of creativity and latitude is required. | 01/06/2025 |
| 1895 | LGC Milford, MA Manufacturing Associate Preferred Bachelor’s degree, with a concentration in Biology, Chemistry, or related science Exp: 1-3 years |
The Manufacturing Associate provides direct labor for the manufacturing of high-quality diagnostic products using manual and semi-automated equipment and prepares/completes required documentation on manufacturing procedures. This position is responsible for set-up, calibration, and operation of all manufacturing equipment in accordance with cGMP, POPs, SOPs, Safety, and departmental policies. This position utilizes good judgment and critical thinking skills to make operator level decisions regarding the quality of the products manufactured. | 01/06/2025 |
| 1896 | LGC Novato, CA GMP Manufacturing Technician I/II/III - Synthesis Bachelor's degree in a related STEM field Exp: 1 year |
The GMP Manufacturing Technician position is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements at the Petaluma and Novato ISO 13485 sites and as directed by the GMP Manufacturing Management. This role will be on our Synthesis team in Novato Lab. | 01/06/2025 |
| 1897 | LGC Novato, CA GMP Manufacturing Technician I/II/III -KIT Lab Bachelor's degree in a related STEM field Exp: 1 year |
The GMP Manufacturing Technician position is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements at the Petaluma and Novato ISO 13485 sites and as directed by the GMP Manufacturing Management. This will be in our Kit Lab in Novato. Techs do final dry down (lyophilizatoin), column packing for purification, aliquoting and kitting of product. | 01/06/2025 |
| 1898 | LGC Remote/Petaluma, CA Field Application Scientist I Bachelor's or Master's degree in Molecular Biology, Biochemistry, Chemistry, Genetics, or related field Exp: 1-3 years |
The Field Service Application Scientist I is a multi-disciplinary molecular biology and organic chemistry position that will contribute to the organization as part of our Global Field Service team, bringing curiosity, problem solving skills, and scientific acumen to LGC. The Field Service team supports various wings of the organization such as Laboratory Operations, Engineering, Sales, and Manufacturing. | 01/06/2025 |
| 1899 | LGC Petaluma, CA Oligonucleotide Production Technician I - Purification Bachelor’s degree in a STEM discipline Exp: 0-2 years |
The Oligonucleotide Production Technician I - Purification will perform tasks associated with the purification of oligonucleotides in a high throughput, time sensitive manufacturing environment. | 01/06/2025 |
| 1900 | Nephron West Columbia, SC Microbiology Environmental Monitoring Trainer Bachelor’s degree with a science background Exp: 1-2 years |
Performs on-the-job, group, and one-on-one trainings with Environmental Monitoring (EM) program personnel. Coordinates and utilizes different departments and resources for task specific trainings. The EM Trainer is an expert on monitoring performed as an EM Technician I, II, and III. Assists with additional work duties or responsibilities as evident or required. | 01/06/2025 |
| 1901 | Neuralink Austin, TX Quality Assurance Specialist Bachelor of Science degree, preferably in a science, engineering, or quality-related discipline Exp: 1 year |
The Quality Assurance (QA) Specialist will work with Neuralink's teams to ensure that the appropriate governing body regulations are followed. This includes, but is not limited to, adherence to ISO standards, Good Laboratory Practices (GLP), clinical guidelines, manufacturing protocols, and quality control practices. | 01/06/2025 |
| 1902 | Neuralink Austin, TX Quality Systems Specialist Bachelor of Science in Engineering or a related field Exp: 1-2 years |
As a Quality Systems Specialist, you will work with teams across the Neuralink organization to resolve isolated and systemic problems through NCRs and CAPAs. You’ll identify ways to trend defects and issues for broader audiences and leadership. This role involves communicating and collaborating with different teams, such as R&D, manufacturing, product, etc., to maintain document/change management and data systems and ensure regulatory compliance with applicable standards. | 01/06/2025 |
| 1903 | Neuralink Fremont, CA Quality Systems Specialist Bachelor of Science in Engineering or a related field Exp: 1-2 years |
As a Quality Systems Specialist, you will work with teams across the Neuralink organization to resolve isolated and systemic problems through NCRs and CAPAs. You’ll identify ways to trend defects and issues for broader audiences and leadership. This role involves communicating and collaborating with different teams, such as R&D, manufacturing, product, etc., to maintain document/change management and data systems and ensure regulatory compliance with applicable standards. | 01/06/2025 |
| 1904 | Neurogene Houston, TX Associate Scientist, Analytical Development BS in Molecular Biology, Biochemistry, Cell Biology, or related field. Exp: 1 year |
Reporting into the Senior Scientist, Analytical Development, the Associate Scientist, Analytical Development plays a critical role in ensuring analytical work is executed consistent with product development timelines for Neurogene’s product pipeline. The candidate will perform routine sample testing according to standard operating procedures to support Process Development activities and process transfer to manufacturing. The selected candidate will have the ability to perform different laboratory techniques as well as superior written/oral communication skills, which are essential for success in this key role in a rapidly growing start-up. Furthermore, the candidate will be self-motivated and able to work both independently and within a collaborative team environment. | 01/06/2025 |
| 1905 | Neurona Therapeutics South SF, CA Research Associate Bachelor’s degree Exp: 1-2 years |
Neurona Therapeutics is a clinical stage biotechnology company based in South San Francisco, CA that was created to develop cell-based therapies for neurological disease. We have an opening for a Preclinical Research Associate who will contribute to ongoing programs and build new animal models to study modulation of neural circuits and support translational development of cellular therapeutics. | 01/06/2025 |
| 1906 | New England Biolabs Ipswich, MA Process Development Scientist I/II Bachelor’s or master’s degree in microbiology, biochemistry, biotechnology, or a related field. Exp: 1-4 years |
We are seeking a highly motivated and detail-oriented Process Development Scientist to join our Cloning & Fermentation Development Team at New England Biolabs (NEB). The successful candidate will play a crucial role in developing and optimizing processes for bacterial and yeast expression systems, contributing to the production of recombinant proteins for various applications. | 01/06/2025 |
| 1907 | NJ Bio Princeton, NJ Scientist, Process Development MS level in Organic Chemistry Exp: 0-2 years |
Under minimal supervision works on multiple steps/multiple projects to execute chemical syntheses from mgs to grams to kilo scales and conduct pilot scale synthesis (kilo scale), purification and characterization of compounds and present results and progress updates to internal and external stakeholders, stay abreast of current literature in scientific areas, maintain equipment, chemical inventory and lab support and Perform duties as required. The incumbent works cross-functionally with internal departments and external resources on process development related issues. The Scientist, Process Development supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate. | 01/06/2025 |
| 1908 | Nkarta South SF, CA Cell Therapy Drug Product Engineer 2 – PD/MSAT Bachelor’s degree in chemical or biochemical engineering or related field Exp: 1+ years |
We are seeking a highly motivated and collaborative Engineer to join the Process Development/Manufacturing Science and Technology (PD-MSAT) team in developing and supporting Nkarta’s pipeline of cellular immunotherapy platform and products. This role will primarily represent CMC in our ongoing clinical operations and drug product development. Priorities will include investigations in support of drug product formulation/filling as well as drug processing characterization activities including technology transfer of drug product processing for clinical and future commercial programs. | 01/06/2025 |
| 1909 | Noah Medical San Carlos, CA Robotics and Controls Engineer M.S. in Mechanical, Controls, Robotics or related Engineering discipline Exp: 1 year |
The Robotics and Controls Team at Noah Medical is dedicated to the development and implementation of safe and high quality control algorithms and software. Comprising seasoned engineers with backgrounds in healthcare and other safety-critical industries, we collaborate with clinical, product, and hardware design teams to deliver user-centric solutions. Joining our team means becoming a part of a dynamic and passionate group dedicated to making a significant impact on the future of healthcare through groundbreaking technology. We are looking for a highly motivated, curious, and independent-thinking individual who is eager to take ownership and to contribute to revolutionizing the world of medical robotics while helping make Noah a great place to work. | 01/06/2025 |
| 1910 | Noah Medical San Jose, CA Test Technician BS in Computer Science, Electrical Engineering, or Industrial Engineering Exp: 1 year |
We are seeking a skilled Test Technician to join our team. The ideal candidate will be responsible for testing and troubleshooting medical robotic systems while adhering to Good Manufacturing Practices (GMP). The successful candidate will have a strong understanding of robotic hardware, sensors, motors, PLC’s, relays, circuit boards, computers, cabling and experience with and testing, excellent troubleshooting skills, and GMP experience. | 01/06/2025 |
| 1911 | Nortech Systems Bemidji, MN Quality Engineer Bachelor's degree Exp: 1-2 years |
Are you seeking a role that supports the delivery of lifesaving devices? Do you enjoy working with cross-functional teams to ensure quality standards are met throughout the production process? Are you interested in a role that Identifies quality issues, recommends solutions, and implements changes to resolve discrepancies? Do you like the rigor of Ensuring that processes adhere to quality standards and regulatory requirements. If any of these resonate with you, we encourage you to explore our Quality Engineer role! | 01/06/2025 |
| 1912 | NorthEast Biolab Hamden, CT Associate Scientist, Central Laboratory Services B.S. in Physiological Science, Epidemiology, Microbiology, Immunology, Genetics, Biology, Molecular Biology, Cell Biology, Biotechnology, Biochemistry Exp: Entry Level |
Gain an overall understanding of drug development and maintenance of the full chain of sample custody for regulatory compliance. Support implementation of Laboratory Information management System (Watson LIMS) for sample management and storage. Sample management and reconciliation, kit preparation and verification, and document preparation related to biological sample collection, storage, and shipment for clinical trials. Streamline inventory management, consumable ordering, and other documentation requests for Quality Assurance Unit. Help maintain ultra-low temperature (ULT) freezers and refrigerators and associated electronic logs and records. Learn bioanalytical techniques for the analysis of drug and biomarkers in biological matrices. Follow appropriate safety and study requirements by reading, understanding, and following Standard Operating Procedures (SOP), Good Laboratory Practices (GLP) requirements, and Sponsor Study protocols. Support business development and marketing activities, foster client relationships, and help onboard new sponsors | 01/06/2025 |
| 1913 | NorthStar Medical Radioisotopes Beloit, WI Quality Control Analyst Bachelor’s Degree in Chemistry, Biology, or other related scientific discipline Exp: 1 year |
The primary role of this position is to conduct and validate various biological and analytical quality control assays associated with the processing of radiopharmaceutical isotopes and drugs to ensure compliance with established standards. This role requires extensive training on radiation safety including ALARA (“as low as reasonably achievable”) principles. The Senior Quality Control Analyst will lead various activities, as further described below. Duties will be completed in compliance with applicable regulatory agency standards. This position supports production in a 24-hour manufacturing facility which means your schedule provides days off during the week when weekend work is required. Early morning, late evening, weekend, and some holiday work will be required with occasional overtime. | 01/06/2025 |
| 1914 | NorthStar Medical Radioisotopes Beloit, WI Radiopharmaceutical Manufacturing Associate Bachelor's Degree in a STEM discipline Exp: 1 year |
The Radiopharmaceutical Manufacturing Associate performs duties to support the development and manufacturing of radiopharmaceuticals for NorthStar operations. This includes equipment preparation, product dissolution, and dispensing of medical radioisotopes while complying with procedures, instructions, and prescribed routines. All duties and responsibilities will be completed in compliance with applicable regulatory agency standards. | 01/06/2025 |
| 1915 | Novavax Gaithersburg, MD Associate Scientist, Downstream Process Development Master's degree in Bio/Chem Engineering, Biology, Chemistry, Pharmaceutical Science, Biochemistry, biophysics, Molecular Biology, Life Sciences, vacci Exp: 1+ years |
We are seeking an Associate Scientist to join our Downstream Process Development group in Gaithersburg, MD. Qualified individuals will be responsible for hands-on execution of downstream chromatography and filtration processes in support of process development, scale-up, process characterization activities, and technical support of cGMP manufacturing for proteins, nanoparticles, and virus-like particle (VLP) based vaccines. The candidate will ensure scientifically sound experimental execution, analysis, and reporting. The candidate will be responsible for drafting technical development reports summarizing critical data. The candidate is expected to be highly self-motivated, well organized, and an innovative thinker focused on execution with a sense of urgency. This position will be located at our Gaithersburg, MD facility | 01/06/2025 |
| 1916 | Noven Miami, FL QC Analyst Bachelor’s Degree (BA/BS) in Chemistry or related field Exp: 1 year |
The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents. | 01/06/2025 |
| 1917 | Novitium East Windsor, NJ Quality Control Analyst Bachelors in Pharmaceutical Sciences / Biology / Chemistry / Microbiology / Chemical / Related Exp: 1 year |
Quality Control Analyst (East Windsor, NJ) (Multiple Openings) Conduct research, analysis, synthesis, and experimentation on substances, for such purposes as product and process development and application, quantitative and qualitative analysis, and improvement of analytical methodologies; conduct testing and analysis of pharmaceutical raw materials like drug substance, excipients and packaging materials to analyze various parameters like assay, dissolution, impurities, related substances, residual solvents using various technical instruments like HPLC, GC, UV spectrometry; Conduct testing and analysis of finished product for different dosage forms like capsules, tablets, powder for oral suspension and solutions. The dosage forms include food supplements like vitamin capsules, mineral tablets, and multivitamin syrups. | 01/06/2025 |
| 1918 | Novitium East Windsor, NJ Instrumentation Engineer Bachelor’s in Instrumentation / industrial / electronics / electrical / mechanical / related Exp: 6 months |
Instrumentation Engineer (East Windsor, NJ) (Multiple Openings) Responsible for Instrument and Equipment’s of entire Plant; Installation, troubleshooting & calibration of instruments such as TOC Analyzer, HMI, PLC, Flow Meters, Temperature controller, transmitter, pressure transmitter, gas analyzer; Maintaining minimal instrument downtime through troubleshooting & maintenance activities; Maintaining data backup, instrument documentation, and Spares Inventory & Annual Maintenance contracts; Pro-active Support for Quality Control, Production & Compliance group’s activities; Follow-ups and closures of instrument Change controls, deviations instrument related incidents, & CAP A (corrective and preventive action); Procurement of qualified equipment’s as per GLP & Pharmacopeia requirements, and responsible for IQ, OQ, DQ and PQ for instruments and manage all paperwork. | 01/06/2025 |
| 1919 | Novo Nordisk Boulder, CO Research Associate - Chemical Development BA/BS or master’s degree in chemistry, Biology or related field Exp: 0 years |
Novo Nordisk Global Nucleic Acid Therapies (GNAT) is seeking highly motivated scientists to join its CMC Chemical Development team in Boulder, Colorado. The candidate will be expected to be a key technical resource developing innovative solutions for scalable syntheses, work-up, purifications, and isolations of oligonucleotides, establishing improvements in purity, yield, reproducibility, throughput and environmental impact. The successful candidate will ideally have a strong organic chemistry understanding with exposure to principles of process development, optimization, scale up and tech transfer into a manufacturing setting. This position will support therapeutic programs in multiple disease areas and will contribute to the development of scalable processes supporting Novo Nordisk oligonucleotide programs. Qualified candidates will be expected to work well in a collaborative team environment and be able to independently execute research across a wide range of oligonucleotide and organic chemistry projects. | 01/06/2025 |
| 1920 | Novo Nordisk West Lebanon, NH Manufacturing Technician Bachelors’ Degree in a science discipline Exp: 0 years |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. | 01/06/2025 |
| 1921 | Novo Nordisk West Lebanon, NH Quality Assurance Area Specialist II Bachelor’s Degree (or equivalent) required, a scientific discipline Exp: 1-3 years |
This position is responsible for performing reviews of manufacturing and support documentation and records to certify compliance with in-house specifications/standards and GMP for all NNUSBPI products. This position has QA signature authority on the review of individual batch records, supporting test records and other ancillary support records. Will be a QA presence on the manufacturing floor. | 01/06/2025 |
| 1922 | Novo Nordisk West Lebanon, NH Quality Assurance Area Specialist I Bachelor’s Degree (or equivalent) required, a scientific discipline Exp: 1 year |
This position will review manufacturing and support documentation and records to certify compliance with in-house specifications/standards and GMP for all NNUSBPI products. This position has QA signature authority on the review of individual batch records, supporting test records and other ancillary support records. Will assist in the internal audit program and be a QA presence on the manufacturing floor. | 01/06/2025 |
| 1923 | OraSure Bethlehem, PA Manufacturing Technician (2nd shift) Bachelors degree Exp: 1-3 years |
Operate semi-automated and automated equipment in the production area at a sufficient rate and quality level. Perform on-line inspection of all components/parts produced. Take corrective action and/or make recommendations to the supervisor. Complete all paperwork and equipment logbooks and review other operator's paperwork for accuracy and completeness as required. Responsible for set-up and shutdown of equipment and work closely with the maintenance department in identifying maintenance and repair needs on the equipment. Provide cross training to operators on all pieces of equipment in the production area. Must follow all GMP and company safety regulations and guidelines. May assist in validation of equipment and be solicited for input into development and manufacturing process improvements. | 01/06/2025 |
| 1924 | Nucleus Radiopharma Rochester, MN Quality Control Technician Bachelor’s degree in chemistry, biology required Exp: 1 year |
The Quality Control (QC) Technician performs assigned laboratory testing in compliance with applicable standard operating procedures (SOPs) and in compliance with U.S. and international regulatory requirements, including FDA, ISO, USP, and NRC guidelines. The QC Technician adheres to current good manufacturing practices (cGMP) and good documentation practices (GDocP) for all analyses. Working collaboratively with other laboratory personnel, the QC Technician coordinates instrument usage and completes laboratory tasks efficiently. The QC Technician completes testing and promptly reports any aberrant results to quality management. They work independently under limited supervision and handle radioactive materials as part of their duties. | 01/06/2025 |
| 1925 | Obsidian Therapeutics Bedford, MA Senior Research Associate, Analytical Development Contractor (Core Testing/Characterization) Masters in immunology/biomedical sciences or a related field Exp: 1+ years |
We’re looking for a highly motivated scientist with experience in primary human cell culture, molecular analytics, and cell-based assays to work with our Analytical Development Core Testing team. You’ll focus on characterizing engineered cell therapy products and supporting Obsidian’s tumor infiltrating lymphocytes (TIL), viral vector and critical materials analytical teams. You’ll support critical studies and experiments to advance Obsidian OBX-115 product understanding and work with various subject matter experts across different functional groups, affording a significant learning opportunity and career development. This position is a six month contract role. | 01/06/2025 |
| 1926 | Ocugen Malvern, PA Clinical Trial Associate BA/BS degree, preferably in life sciences. Exp: 1+ years |
The Clinical Trial Associate supports the operational execution of clinical studies. This individual will be responsible for the successful delivery of clinical studies including conducting LDNA tests for clinical studies according to agreed cost and timelines while ensuring patient safety and data integrity and quality. | 01/06/2025 |
| 1927 | Masimo Irvine, CA Engineer, Failure Analysis Bachelor’s degree, preferably in Electrical Engineering, or equivalent Exp: 0-1 years |
Responsible for performing failure analysis of customer returned products, newly manufactured products, and prototype products, with the intent of root cause isolation of full device system issues or sensor and cable issues down to the circuit board, component, or process level. Works closely with Compliance, Regulatory, R &D Engineering, Operations and QA at various levels within the organization to understand the root cause of product failures and identify product improvements | 12/30/2024 |
| 1928 | Masimo Irvine, CA Clinical Research Associate Bachelor’s degree, preferable in Science or in a related field is required Exp: 1-3 years |
The Clinical Research Associate is responsible for clinical studies, site management and compliance monitoring of assigned clinical projects undertaken in support of a given product line or marketing initiative. This position must ensure that all activities will be conducted in accordance with Government Regulations (FDA, MDD and International), Good Clinical Practices (GCP) and Department Operating Procedures (DOP). | 12/30/2024 |
| 1929 | MaxCyte Rockville, MD Software Engineer B.S. in Computer Science, Computer Engineering, or Electrical Engineering Exp: 0-3 years |
Join MaxCyte as a Software Engineer and be at the forefront of developing cutting-edge instrument software and applications, including intuitive UIs and advanced instrument control layers. You’ll be involved in every stage of the software lifecycle, from initial concept to final commercialization, ensuring our life sciences tools are best-in-class. This role offers a unique opportunity to work on innovative projects that make a real impact in the world of biotechnology. Additionally, as a key member of a high-performing team, you’ll have ample opportunities to learn and grow, staying updated with the latest technologies and industry trends. | 12/30/2024 |
| 1930 | MaxCyte Rockville, MD Electrical Engineer B.S. in Electrical Engineering (M.S. preferred) Exp: 0-3 years |
Join MaxCyte as an Electrical Engineer and be at the forefront of developing cutting-edge instrument electronics, including high-speed/high-voltage systems, power electronics, data acquisition, signal processing, and start-of-the-art sensors. You’ll be involved in every stage of the instrument lifecycle, from initial concept to final commercialization, ensuring our life sciences tools are best-in-class. This role offers a unique opportunity to work on innovative projects that make a real impact in the world of biotechnology. Additionally, as a key member of a high-performing team, you’ll have ample opportunities to learn and grow, staying updated with the latest technologies and industry trends. | 12/30/2024 |
| 1931 | Meadowhawk Biolabs Marlborough, MA Research Associate I LCMS Bionanalysis Bachelor’s degree in chemistry, biochemistry, pharmaceutical sciences, or another related scientific field Exp: No Exp |
Meadowhawk Biolabs is seeking a highly motivated and dynamic Research Associate to work within the Discovery Bioanalytical Team at our Marlborough, MA location to perform LC-MS/MS assays in a fast-paced team environment. The ideal candidate is driven, hardworking, willing to learn, dedicated, and passionate about science. Given that we are a newly launched Contract Research Organization (CRO) founded by an experienced team of industry veterans, this ground floor position offers unique opportunities for the successful candidate to contribute meaningfully to the creation and development of our services, expand their knowledge base by participation in multidisciplinary teams, and advance their career in capabilities and responsibilities. | 12/30/2024 |
| 1932 | Meadowhawk Biolabs Marlborough, MA Research Associate II, LCMS Bioanalysis Bachelor’s degree in chemistry, biochemistry, pharmaceutical sciences, or another related scientific field Exp: 1 year |
Meadowhawk Biolabs is seeking a highly motivated and dynamic Research Associate II to work within the Discovery Bioanalytical Team at our Marlborough, MA location to perform LC-MS/MS assays in a fast-paced team environment. The ideal candidate is driven, hardworking, willing to learn, dedicated, and passionate about science. Given that we are a newly launched Contract Research Organization (CRO) founded by an experienced team of industry veterans, this ground floor position offers unique opportunities for the successful candidate to contribute meaningfully to the creation and development of our services, expand their knowledge base by participation in multidisciplinary teams, and advance their career in capabilities and responsibilities. | 12/30/2024 |
| 1933 | Medpace Irving (Dallas), TX Clinical Data Coordinator - Biology Degree Bachelor's degree in a Life Science or related field Exp: Entry Level |
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Coordinator to join our Data Management team. This position involves working on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your knowledge and experience to further develop and grow your career even further, then this is the opportunity for you! | 12/30/2024 |
| 1934 | Medpace Irving (Dallas), TX Clinical Data Coordinator - Chemistry Degree Bachelor's degree in a Life Science or related field Exp: Entry Level |
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Coordinator to join our Data Management team. This position involves working on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your knowledge and experience to further develop and grow your career even further, then this is the opportunity for you! | 12/30/2024 |
| 1935 | Medpace Irving (Dallas), TX Clinical Data Coordinator - Mathematics Degree Bachelor's degree in a Life Science or related field Exp: Entry Level |
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Coordinator to join our Data Management team. This position involves working on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your knowledge and experience to further develop and grow your career even further, then this is the opportunity for you! | 12/30/2024 |
| 1936 | Medpace Irving (Dallas), TX Clinical Research Project Coordinator - Entry Level Bachelor's degree in a Life Science or related field Exp: Entry Level |
Medpace is a leading CRO for Biotech companies and we are currently seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. Our therapeutic areas of focus include Oncology/Hematology, Cardiovascular/Metabolic/Renal, Infectious Disease/CNS/Ophthalmology and more. If you are looking for a fast paced, collaborative work environment in clinical research and want to develop your career even further, then this is the opportunity for you. Medpace provides Project Coordinators a 4-6 week training program that incorporates a virtual and hands on learning experience, especially for those without previous clinical research experience. | 12/30/2024 |
| 1937 | Medpace Cincinnati, OH Senior Data Scientist Master’s degree in informatics, computer science/engineering, health information, statistics, or related field Exp: 1-2 years |
We are currently seeking an experienced data scientist to join our Informatics team who will lead advanced analyses of methodological data to inform study design decisions. The Informatics team utilizes informatics principles and techniques to architect, mine, analyze, and visualize clinical trial data to inform study design choices for pharmaceutical development. The informaticist will create predictive data models to identify and analyze patterns, then program compelling visualizations of the data to support feasibility strategies. The team is seeking an experienced candidate for a senior-level position to contribute new skills to our team, sopport team growth and foster fellow analyst development. | 12/30/2024 |
| 1938 | Medtronic Fridley, MN Process Engineer II Master's degree in Engineering Exp: 0 years |
The Rice Creek Pharma Operations Advanced Manufacturing Engineering Process Engineer II is responsible for evaluating, improving, and controlling the overall performance of manufacturing areas that provide implantable components and finished devices, including combination products. This role involves leading and collaborating closely with Operations, Quality, Reliability Engineering, and Regulatory Affairs. The Process Development Engineer plays a crucial role in introducing new processes into manufacturing and providing technical solutions to product performance issues. | 12/30/2024 |
| 1939 | Medtronic Tempe, AZ Materials Engineer II Master's degree in Engineering Exp: 0 years |
Engineers are indispensable to achieving our Mission. That’s why we empower you to bring the best of your experience to bear on our market-leading portfolio of innovations. Apply your existing skills and develop new ones, with the training, mentorship, and the guidance you need to continue to develop your expertise. As a Materials Engineer II, you will be responsible for performing physical analysis of electronic components and medical devices, developing analysis techniques, and supporting analysis tools in a laboratory setting. You will have hands on responsibilities on multiple tools and you will collaborate across multiple engineering disciplines. | 12/30/2024 |
| 1940 | Medtronic Brooklyn Center, MN Quality Engineer II Master's degree in Engineering Exp: 0 years |
The Brooklyn Center facility also known as Medtronic Electronics Components Center (MECC) supports the production of components used in devices for a variety of Medtronic Operating Units (OUs). This role reports to the Operations Quality Manager at MECC. Key aspects of this role include executing the disposition and closure of nonconformances in a timely fashion, collaborating with customer sites (downstream Medtronic facilities) on non-conformance investigation and resolution, participating in a culture of collaboration and compliance in one of the Components Focus Factory (Includes Connectors/Molding, Capacitors, TDCO, and Feedthroughs), execute day to day operations, and execute continuous improvement/programmatic savings initiatives to reduce the overall quality risk within a specific Focus Factory. | 12/30/2024 |
| 1941 | Medtronic Los Angeles, CA Electrical Engineer II Master's degree in Electrical Engineering Exp: 0+ years |
In this exciting and challenging role as a test engineer, your responsibilities will include Designing, developing, and implementing testing methods and equipment. Plans and arranges schedules, and equipment required for verifying products. Provides test area with parameters for sample testing and specifies tests to be performed. Compiles data and defines changes required in testing equipment, testing procedures, manufacturing processes, or new testing requirements. Responsible for writing verification test plans and reports. This will be a hybrid position which requires person to be on site for test method development and supervising of product verification testing. | 12/30/2024 |
| 1942 | Medtronic Brooklyn Center or Minneapolis, MN Battery Manufacturing Engineer II Master's degree in Engineering Exp: 0 years |
In this exciting role as a Battery Manufacturing Engineer II at Medtronic’s Energy & Component Center (MECC), you will have responsibility for supporting and improving the manufacturing of the high quality batteries used in implantable medical devices. You will be responsible for day to day production support, new process development support and lead improvement projects. The Brooklyn Center facility supports the design, development, and production of components used in implantable devices for a variety of Medtronic businesses. In this role you will gain experience with products across Medtronic’s portfolio, supporting your development and growth. This role is responsible for improving manufacturing quality, lead time and cost through active problem solving, developing solutions and implementing process changes in accordance with the quality system. What does it take to be a leader at Medtronic? We look for inspiring and inclusive leaders who partner with others, knowing that diverse talent, skills, and perspectives lead to better outcomes. Please note this role does work on-site in the manufacturing area. | 12/30/2024 |
| 1943 | Medvacon Winchester, KY QC Analyst Bachelors degree in Chemistry, Biology, Chemical Engineering or Life Sciences Exp: 0-5 years |
A QC Analytical chemist is an entry level position for individuals who use their understanding of science to perform the basic and critical experimental work of day-to-day analysis, including generation and analysis of data. Their work is “hands on” in an analytical lab and requires analytical testing, computer operating, record keeping, and report writing abilities. This position performs the quality testing needed for raw material, in-process, finished goods, stability, and cleaning validation analysis. | 12/30/2024 |
| 1944 | Meissner Camarillo, CA R&D Scientist I Bachelor’s degree required in STEM-related field Exp: 1-5 years |
At Meissner, we provide B2B technical solutions, that are deployed to improve the human condition. Our customers use our products and technologies to develop new therapeutics and many familiar products that support our modern lifestyle. At the core of these products, are in-house technologies that are developed and maintained by highly talented and self-driven engineers and scientists. Projects are typically heavily weighted towards chemical processes and materials science at an R&D/prototype scale to pilot and production scales. The R&D Scientist will undertake independent research projects and/or investigations or be responsible with specific parts of larger projects, with a higher degree of independence. | 12/30/2024 |
| 1945 | Merck West Point, PA Assoc. Scientist, Analytical R&D Bachelor’s degree or higher in biology, chemistry, biochemistry, bio-engineering or related sciences Exp: 1 year |
We are seeking a growth and improvement minded Associate Scientist that can help drive our Strategic Operating Priorities working as a Subject Matter Expert with live virus vaccine potency assays. We are seeking a highly motivated colleague to join our team as a scientist supporting our inline and pipeline vaccine programs. This position will work in a GMP environment and will be expected to execute various cell-based assays in a high throughout environment. The candidate will work with a large team of colleagues to deliver high quality results for multiple vaccine products. This position will require work with various instrumentation to develop new methods in line with current technologies. | 12/30/2024 |
| 1946 | Merck West Point, PA Scientist, Laboratory Animal Resources Bachelor's degree Exp: 1+ year |
Our company a global healthcare leader, is currently seeking an Entry-Level Laboratory Animal Resources Associate to join our collaborative, dynamic, and inclusive Laboratory Animal Science Team at the West Point location. The successful candidate will be integral in planning, designing, and executing in vivo ophthalmology research, as well as some routine veterinary and animal colony management tasks. On-site and hands-on study-related lab work will be a crucial part of the role. The role also requires rotation weekend work and the ability to apply sound technical skills to assigned tasks, often with minimal supervision. | 12/30/2024 |
| 1947 | Meridian Bioscience Memphis, TN Quality Assurance Associate Bachelor’s degree in life science, chemistry, pharmaceutical science, statistics, or health/human services related field. Exp: 0-5 years |
The Quality Assurance (QA) Associate will support QA processes, programs, and conduct QA activities. This position will uphold standards, methods, and procedures for all stages of production. This position will identify continuous process improvement areas, in compliance with Good Manufacturing Practices (GMP) and Good Documentation Practices (GLP) processes and documentation for quality control activities. This requires excellent technical skills and abilities, analytical and mathematical skills, organizational and time-management skills, verbal, and written communication skills, plus ability to apply attention to detail. | 12/30/2024 |
| 1948 | Meridian Bioscience North Billerica, MA Quality Control Technician Bachelor’s degree in a life science (Biology, Microbiology, etc.) Exp: 0-2 years |
Responsible for ensuring materials, processes, and products meet the required specifications, which involves, but is not limited to, inspections, metrology testing, documentation, and labeling reviews. Product acceptance or rejection. Responsible for maintaining equipment calibration. | 12/30/2024 |
| 1949 | MethodSense Morrisville, NC Quality and Safety Engineer Bachelor’s degree in biomedical engineering or alternative engineering degree. Exp: 1-7 years |
We are looking for talented Quality and Safety Engineers to join our experienced team. If you can commit yourself to supporting a passionate regulatory affairs and quality assurance business dedicated to their clients, you can have a career with us. We need someone with honesty, integrity and excellent communication and interpersonal skills. The position requires the ability to work with client company executives, test labs and FDA regulators. It also requires agility and love for knowledge. If you want to join a high energy purposed team, please apply. | 12/30/2024 |
| 1950 | Minaris Regenerative Medicine Mountain View, CA QC Analytical Associate I BA/BS in a science or relevant field required Exp: 0-2 years |
The Quality Control Analytical Associate serves as a support role to clinical and commercial production. The QC Analytical Associate will assist with process check point, stability, and release analytical testing to ensure that quality standards are upheld for all products produced at the facility. | 12/30/2024 |
| 1951 | Minaris Regenerative Medicine Allendale, NJ QA Associate II BS or higher education degree in a scientifically related field Exp: 1-3 years |
The Quality Assurance Associate plays a pivotal role in ensuring that all quality assurance activities are conducted efficiently and accurately. Under direct supervision, the associate supports daily tasks that are essential for maintaining and improving quality systems and adhering to client-specific procedures. Key responsibilities include document management, review of manufacturing batch records, quality control (QC) data, facilitating material releases, overseeing final product releases, and providing essential assistance to the Quality Management as needed. | 12/30/2024 |
| 1952 | Modulo Bio San Diego, CA Stem Cell Scientist MS in Genetics, Molecular Biology, Developmental Biology, Biochemistry, Regenerative Medicine, Neuroscience, or related field Exp: 1+ years |
Modulo Bio is seeking a Stem Cell Scientist to develop and scale an induced-pluripotent stem cell (iPSC)-based in vitro model of the neuroimmune system. Modulo Bio is building a proprietary immune cell modeling platform, which incorporates human genetics, functional genomics, molecular biology, cellular and tissue profiling, disease model engineering, and advanced computational models. The successful candidate will build a complex cell model platform with the goal of improving our understanding of human biology and therapeutic interventions to inform early and late stage pipeline efforts. Candidates with an eagerness to work within a highly leveraged, team-driven, dynamic research environment will be prioritized. The candidate will work in close collaboration with our internal Computational Biology group which is focused on next-generation sequencing (NGS), functional genomics, cell or tissue profiling, and bioinformatics analyses of cutting-edge large-scale genetic screening or single-cell technologies to enhance our analytic capabilities and to reveal the underlying mechanisms of human disease. | 12/30/2024 |
| 1953 | Molecular Assemblies San Diego, CA Research Associate II / Associate Scientist- Biochemistry M. S. in Biochemistry, Chemistry, Molecular Biology, or a related field. Exp: 1+ years |
The R&D organization is seeking a highly motivated and detail-oriented Associate Scientist to join the biochemistry team. In this role, you will work closely with senior scientists to support the development of high-fidelity, template-independent enzymatic synthesis of nucleic acids. The ideal candidate will have a foundational understanding of enzymology and kinetics and laboratory experience in biochemical assays. We are looking for someone who thrives in a fast-paced environment and is passionate about scientific discovery and innovation. This role is onsite 5 days a week. | 12/30/2024 |
| 1954 | Molecular Designs Birmingham, AL Lab Technician- Night Shift Bachelor’s degree in Biology, Chemistry, Biochemistry Exp: 6 months |
We're looking for a Molecular Lab Technician (MLT) to help with day-to-day screening procedures for our molecular testing laboratory. We’re seeking a highly driven, motivated, and experienced Lab Technician that understands the PCR process, its importance, and work through each complex step with the upmost efficiency. The ideal Lab Technician will have patience, empathy, time management, and professionalism with patients, co-workers, and providers. | 12/30/2024 |
| 1955 | Molecular Designs Birmingham, AL Quality Assurance Specialist Bachelor’s Degree in biology or related sciences preferred Exp: 1-2 years |
The Quality Assurance Specialist is responsible for supporting the Manager of Quality with implementing and maintaining all aspects of the quality management system. This position requires a person to perform various tasks (but not limited to) within the quality department including Documentation Control (manual and electronically), Corrective Actions, Nonconforming Product, assist with creation of Device Master Records, control of Device History Files, Quality Metrics and SOP/Work Instruction Development. | 12/30/2024 |
| 1956 | Moog Buffalo, NY Development Electrical Engineer Master’s Degree in Engineering Exp: 1+ years |
The Test Systems Electrical Development Engineer will contribute to the analysis, conceptual design, development, and test of complex control systems' electrical components. These systems will be used for qualification and acceptance testing of Moog's military aircraft control system products. The products of Moog generally are unique for each customer. Therefore, most new applications require a special, tailored design, even though adaptation of existing designs always are considered where appropriate. The Development Engineer will operate as part of a multi-disciplinary design and development team. You may coordinate the work of drafters, technicians, vendors, and others who support new designs. In the early stages of a new program, the project team will consult with the customer, establish the problem statement, conceive of potential hardware solutions to the problem, and then create a successful technical proposal. Under the technical direction of the team's lead Engineer, the Development Engineer will then contribute to the evolution of the conceptual design, technical project planning, detail design, and testing (risk mitigation, integration, and validation/verification). | 12/30/2024 |
| 1957 | Moog Salt Lake City, UT Research & Development Engineer Bachelor’s degree (B.S.) in related electromechanical, biomedical engineering, or technical discipline Exp: 1 year |
As a R&D Engineer you will perform engineering verification and validation testing activities within FDA QSR standards with guidance of senior engineering. Reporting to the Manager Senior, Engineering you will be located in Salt Lake City, Utah. | 12/30/2024 |
| 1958 | Novartis Morris Plains, NJ Cell Processing Specialist I Bachelor’s degree in relevant Engineering or Scientific discipline Exp: 1 year |
The Cell Processing Specialist is responsible for cell washing operations and verifying cell processing intermediate processing days of patient derived clinical and commercial cellular immunotherapy products. The CPS I will also be responsible for the formulation and verification of all media lots. Due to the nature of the starting material (patient cells) this role requires high level of proficiency and ownership of the process and media formulation. | 12/30/2024 |
| 1959 | Novartis Morris Plains, NJ Associate Scientist, Raw Materials Bachelor’s degree or MS in Biology, Chemistry, Biochemistry, Microbiology or other related science Exp: 1 year |
Under general direction; the Associate Scientist, Raw Material will direct and assist in functions supporting QC raw materials. | 12/30/2024 |
| 1960 | Novartis East Hanover, NJ Expert - Molecular Biology M.S. in Molecular Biology or closely related discipline Exp: 1 year |
As a key member of the Analytical Development team, this individual will support developmental activities to aid in delivering gene therapy to patients. The successful candidate will support technical and development projects designed to characterize gene therapy products through an assortment of analytical methods. This role will also contribute to cross-functional activities including monitoring and characterizing of processes and products to identify opportunities for continuous improvement. Growth mentality and passion to serve patients, his/her technical team and development programs is a must. | 12/30/2024 |
| 1961 | Novartis Millburn, NJ Production Technician I Bachelor’s degree in relevant Engineering or Scientific discipline Exp: 1+ years |
Production Technicians play an active role in daily production of Radioligand Therapies (RLT) as well as setup and preparation of instruments and equipment. The Production Technician adheres to regulatory requirements while performing job functions, executing production as per batch records and SOPs. Responsibilities are performed within a team and according to an assigned production shift schedule. The Production Technician works closely with the Manager and Lead to ensure production is executed in a safe and timely manner. | 12/30/2024 |
| 1962 | Novartis Indianapolis, IN Production Technician I Bachelor’s degree in relevant Engineering or Scientific discipline Exp: 1+ years |
Production Technicians play an active role in daily production of Radioligand Therapies (RLT) as well as setup and preparation of instruments and equipment. The Production Technician adheres to regulatory requirements while performing job functions, executing production as per batch records and SOPs. Responsibilities are performed within a team and according to an assigned production shift schedule. The Production Technician works closely with the Manager and Lead to ensure production is executed in a safe and timely manner. | 12/30/2024 |
| 1963 | Novartis Durham, NC Bioprocess Technician/Engineer (Upstream Nights) Bachelor of Science Degree in Biology, Chemistry, Biotechnology or applicable field Exp: Entry Level |
The BioProcess Technician or Engineer I/II/III is responsible for assisting with organizing, running, and sustaining the manufacturing operations process at the plant/site. The level of the role will be determined by the years of relevant experience. Novartis Gene Therapies is dedicated to developing and commercializing gene therapies for patients and families devastated by rare and life-threatening neurological genetic diseases. | 12/30/2024 |
| 1964 | Novartis Morris Plains, NJ QC Microbiology Technician Bachelor’s in Microbiology or closely related field Exp: 1 year |
The QC Microbiology Technician is responsible for assisting routine and batch-related Environmental Monitoring in controlled environments, following current Good Manufacturing Practices. | 12/30/2024 |
| 1965 | Myomo Burlington, MA Quality Engineer II Bachelor's degree in a related Engineering discipline Exp: 1+ year |
The Quality Engineer provides support to the QC Engineering Manager and team. The core aspects of this role are to focus on non-conforming materials, establish effective inspection methods, resolve supplier quality issues, and collaborate with Product Development to deliver effective product testing, validation, and inspection.He/she will also assist in the implementation of appropriate systems, policies, and procedures to ensure quality and compliance and proactively develop improved processes. The ideal candidate is a well-organized, process-oriented, and systematic-minded professional who is able to keep an eye toward process improvements and innovation. Keys to success in this role include the ability to demonstrate attention to detail as well as the capability to both collaborate effectively and work independently. He/she will be able to understand and incorporate the viewpoints of cross-functional stakeholders. | 12/30/2024 |
| 1966 | Myriad Genetics Salt Lake City, UT Lab Technologist II - Precise Lab Bachelor’s, or Master’s degree in medical technology or a chemical, physical, biological Exp: 6 months |
The Lab Technologist II is responsible for conducting laboratory processes that support specimen processing and testing. This position works with department management and quality team members to ensure that laboratory activities are defined, documented, and completed to support inspection readiness and that compliance is maintained through procedures, training, documentation, and continuous improvement projects. | 12/30/2024 |
| 1967 | KVK Tech Newtown, PA QA Technical Reviewer Bachelor’s degree in Chemistry or a related field preferred Exp: 1-2 years |
The QA Technical Reviewer will be responsible for GMP review and comment on laboratory raw data, procedures and reports to ensure methods, protocols and other procedures were properly followed, results are analytically accurate and correct, and that all documentation meets GMP standards. | 12/16/2024 |
| 1968 | Kyowa Kirin Sanford, NC Project Engineer I Bachelor’s degree in engineering Exp: 1 year |
The Project Engineer will play a key in the design, construction, and start-up of a new manufacturing facility. Working directly with the Site Head during the project phases, the Project Engineer will transition into an operational role within the plant. This role will partner closely with the Site Leadership Team, gaining a comprehensive understanding of various functions and managing a range of projects to build both depth and breadth of experience across the site. This position will provide hands-on involvement in designing, developing, and operationalizing the facility from the ground up. | 12/16/2024 |
| 1969 | Leidos Remote, Transmission Reliability Engineer Bachelors in Electrical Engineering or related engineering degree is required Exp: 0+ years |
Leidos Engineering is seeking a Transmission Reliability Engineer to join our System Planning team. This role will involve the execution of transmission planning, transmission system modeling, compliance verification, and protective device coordination, as project and client criteria dictate. Successful candidates can expect to conduct Transmission system software modeling and analysis studies for Municipal Utilities, Investor-Owned Utilities, and Regional Planning organizations. The position will involve some degree of client-facing work, with some business development activities to be expected. The growth potential of this position is significant for a well-qualified candidate. | 12/16/2024 |
| 1970 | Leidos Pittsburgh, PA Associate Distribution Engineer Bachelors of Science in Engineering degree or Master’s degree (EE or CE preferred) Exp: 0+ years |
The successful candidate will have an interest in developing construction work packages for the electric distribution system using various software systems and construction standards. Distribution systems may be in an OH, UG, or URD environment. Project work may include joint use make ready, and street light projects. Work packages will be developed using Geographic Information Systems (GIS), Computer Aided Design (CAD) tools, Work Management Systems (WMS), and other client systems. Project work will require performing engineering calculations that may include: structural analysis of poles, guying, cable pulling, electric demand, transformer sizing, voltage drop and flicker, and coordination of protective devices. Assignments may also include: preparing forestry trimming requests, facilitating permit and Right-of-Way acquisition, development of a BOM, estimating costs, and customer advocacy such as acquiring easements. Work assignments will include travelling by motor vehicle to various project locations located throughout the area to conduct field investigations. The associate level candidate need not be proficient in applicate customer engineering, construction standards, and software systems. Training will be provided by Leidos. | 12/16/2024 |
| 1971 | Leidos Piscataway, NJ Associate Distribution Engineer Bachelors of Science in Engineering degree or Master’s degree (EE or CE preferred) Exp: 0+ years |
The successful candidate will have an interest in developing construction work packages for the electric distribution system using various software systems and construction standards. Distribution systems may be in an OH, UG, or URD environment. Project work may include joint use make ready, and street light projects. Work packages will be developed using Geographic Information Systems (GIS), Computer Aided Design (CAD) tools, Work Management Systems (WMS), and other client systems. Project work will require performing engineering calculations that may include: structural analysis of poles, guying, cable pulling, electric demand, transformer sizing, voltage drop and flicker, and coordination of protective devices. Assignments may also include: preparing forestry trimming requests, facilitating permit and Right-of-Way acquisition, development of a BOM, estimating costs, and customer advocacy such as acquiring easements. Work assignments will include travelling by motor vehicle to various project locations located throughout the area to conduct field investigations. The associate level candidate need not be proficient in applicate customer engineering, construction standards, and software systems. Training will be provided by Leidos. | 12/16/2024 |
| 1972 | Leidos Edison, NJ Associate Distribution Engineer Bachelors of Science in Engineering degree or Master’s degree (EE or CE preferred) Exp: 0+ years |
The successful candidate will have an interest in developing construction work packages for the electric distribution system using various software systems and construction standards. Distribution systems may be in an OH, UG, or URD environment. Project work may include joint use make ready, and street light projects. Work packages will be developed using Geographic Information Systems (GIS), Computer Aided Design (CAD) tools, Work Management Systems (WMS), and other client systems. Project work will require performing engineering calculations that may include: structural analysis of poles, guying, cable pulling, electric demand, transformer sizing, voltage drop and flicker, and coordination of protective devices. Assignments may also include: preparing forestry trimming requests, facilitating permit and Right-of-Way acquisition, development of a BOM, estimating costs, and customer advocacy such as acquiring easements. Work assignments will include travelling by motor vehicle to various project locations located throughout the area to conduct field investigations. The associate level candidate need not be proficient in applicate customer engineering, construction standards, and software systems. Training will be provided by Leidos. | 12/16/2024 |
| 1973 | Leidos Framingham, MA (Entry Level) Civil/Structural Engineer Bachelors of Science (BS) degree in Civil-Structural Engineering Exp: 0-2+ years |
We are seeking an Entry Level Civil/Structural Engineer with 0-2+ years of experience with a utility and/or utility consulting company doing design engineering. The candidate must have a strong educational background in design of steel structures, concrete structures, geotechnical engineering, and foundations. | 12/16/2024 |
| 1974 | Leidos Walled Lake, MI (Entry Level) Civil/Structural Engineer Bachelors of Science (BS) degree in Civil-Structural Engineering Exp: 0-2+ years |
We are seeking an Entry Level Civil/Structural Engineer with 0-2+ years of experience with a utility and/or utility consulting company doing design engineering. The candidate must have a strong educational background in design of steel structures, concrete structures, geotechnical engineering, and foundations. | 12/16/2024 |
| 1975 | Leidos Honolulu, HI Associate Distribution Engineer Bachelors of Science in Engineering degree or Master’s degree (EE or CE preferred) Exp: 0+ years |
Leidos is seeking an Associate Distribution Engineer in our Honolulu, HI office. The selected candidate will be required to work for a Leidos contractor for a period of 6 months with the possibility of converting to full-time direct Leidos employment. The successful candidate will have an interest in developing construction work packages for the electric distribution system using various software systems and construction standards. Distribution systems may be in an OH, UG, or URD environment. Project work may include grid hardening and reliability, substation optimization, joint use make ready and street light projects. Work packages will be developed using Geographic Information Systems (GIS), Computer Aided Design (CAD) tools, Work Management Systems (WMS), and other client systems. Project work will require performing engineering calculations that may include: structural analysis of poles, guying, cable pulling, electric demand, fault currents, and coordination of protective devices. Assignments may also include: preparing forestry trimming requests, facilitating permit and Right-of-Way acquisition, development of a BOM, estimating costs, and customer advocacy such as acquiring easements. | 12/16/2024 |
| 1976 | LFB USA Charlton, MA Manufacturing Technician II Bachelor’s Degree Exp: 1-3 years |
LFB USA has an immediate need in our Manufacturing group for a Manufacturing Technician. Level will be based upon experience. Responsible for the commercial production of drug intermediates (protein purification, buffer/equipment preparation), intended for further manufacture of drug products. This is a senior technician position in a regulated biomanufacturing setting. | 12/16/2024 |
| 1977 | LFB USA Charlton, MA Manufacturing Technician III Bachelor’s Degree Exp: 1-3 years |
LFB USA has an immediate need in our Manufacturing group for a Manufacturing Technician. Level will be based upon experience. Responsible for the commercial production of drug intermediates (protein purification, buffer/equipment preparation), intended for further manufacture of drug products. This is a senior technician position in a regulated biomanufacturing setting. | 12/16/2024 |
| 1978 | LGC Remote/Alexandria, MN Field Application Scientist I Bachelor's degree in Molecular Biology, Biochemistry, Chemistry, Genetics, or related field Exp: 1-3 years |
The Field Service Application Scientist I is a multi-disciplinary molecular biology and organic chemistry position that will contribute to the organization as part of our Global Field Service team, bringing curiosity, problem solving skills, and scientific acumen to LGC. The Field Service team supports various wings of the organization such as Laboratory Operations, Engineering, Sales, and Manufacturing. The scope of this position will include field-based customer support, customer assay verification/validation on LGC instrumentation, scientific support for applications development of our technologies, and providing various levels of technical support on our instrumentation and software. As part of this role, the Field Service Application Scientist I will have excellent customer-facing skills combined with a strong understanding of LGC products, including instrumentation and reagents. They will be required to operate laboratory equipment, on-site install of instrumentation, develop testing protocols, troubleshoot, analyse data, and keep current on emerging technologies in the fields of molecular biology, as well as organic chemistry. This position will be developed in a fusion of knowledge from genomics, PCR-based genetic analysis, laboratory automation, Oligo synthesis, DNA extraction, and customer support. | 12/16/2024 |
| 1979 | LGC Novato, CA GMP Manufacturing Technician I/II/III -KIT Lab Bachelor's degree in a related STEM field Exp: 1 year |
The GMP Manufacturing Technician position is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements at the Petaluma and Novato ISO 13485 sites and as directed by the GMP Manufacturing Management. This will be in our Kit Lab in Novato. Techs do final dry down (lyophilizatoin), column packing for purification, aliquoting and kitting of product. | 12/16/2024 |
| 1980 | LGC Novato, CA GMP Manufacturing Technician I/II/III - Synthesis Bachelor's degree in a related STEM field Exp: 1 year |
The GMP Manufacturing Technician position is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements at the Petaluma and Novato ISO 13485 sites and as directed by the GMP Manufacturing Management. This will be in our Synthesis department in our Novato Lab. | 12/16/2024 |
| 1981 | LGC Petaluma, CA Oligonucleotide Production Technician I - Purification Bachelor's degree in a related STEM field Exp: 0-2 years |
The Oligonucleotide Production Technician I - Purification will perform tasks associated with the purification of oligonucleotides in a high throughput, time sensitive manufacturing environment. Operates HPLC and/or RPC instruments. Comprehend chromatography techniques. Utilizes mass spectrometry and spectrophotometer instruments to obtain crude data. Schedule/Core Hours – Tues-Fri swing shift (1pm-11pm) schedule | 12/16/2024 |
| 1982 | LGC Clinical Diagnostics Milford, MA Manufacturing Associate Bachelor’s degree, with a concentration in Biology, Chemistry, or related science Exp: 1-3 years |
The Manufacturing Associate provides direct labor for the manufacturing of high-quality diagnostic products using manual and semi-automated equipment and prepares/completes required documentation on manufacturing procedures. This position is responsible for set-up, calibration, and operation of all manufacturing equipment in accordance with cGMP, POPs, SOPs, Safety, and departmental policies. This position utilizes good judgment and critical thinking skills to make operator level decisions regarding the quality of the products manufactured. | 12/16/2024 |
| 1983 | LifeSensors Malvern, PA Cellular/Molecular Biologist BS/MS in biological sciences. Exp: 0-10 years |
LifeSensors, Inc. is a global leader in research involving the Ubiquitin Proteasome System (UPS) a cellular pathway that degrades damaged proteins. UPS provides a challenge as a new wave of drugs are emerging, such as PROtein TArgeting Chimeras (PROTACs) and Molecular Glues that target undruggable space. Our technologies are used worldwide by academic, pharma and biotech companies. As the company grows, it is critical that we continue to innovate. The scientist will be a part of research programs to develop innovative technologies, execute drug discovery projects for our clients, as well as drive the development of new products and product applications. They will write scientific articles, patents, and present data at national and international meetings. Please consult our website www.lifesensors.com for more details. | 12/16/2024 |
| 1984 | LivaNova Houston, TX Microbiology Technician Bachelor's Degree in Biology or related with completed coursework in Microbiology preferred Exp: No Exp |
This position is responsible for microbiological testing for the release of sterilization loads, for the periodical environmental monitoring of clean room areas and sterile barrier packing process of the devices. Successful candidate will work under general supervision to prepare all the microbiological media needed for in-house testing and as needed, to perform microbiological tests, environmental monitoring and packaging process tests which require standard procedures and instrumentation. | 12/16/2024 |
| 1985 | Alexion New Haven, CT Associate Scientist II, Injectable Drug Product Development MS degree, Biochemistry, Chemistry, Chemical Engineering or related discipline Exp: 1+ year |
The Associate scientist II will join Injectable Drug Product Development group to support the development of Alexion’s biotherapeutic candidates. This individual will design and execute experiments to develop injectable drug product formulations and process characterization studies, including analyzing samples and authoring technical reports. This individual will work in a dynamic team environment and routinely collaborate with other members of Injectable Drug Product Development as well as other groups in Product Development and Clinical Supply. | 12/16/2024 |
| 1986 | Lonza Portsmouth, NH QC Scientist I-Technical Transfer Bachelor's degree required; Advanced Graduate Degree (MS/PhD) preferred Exp: 0-4 years |
Lonza AG is thrilled to offer an outstanding opportunity for a Quality Control Scientist 1- Technical Transfer in our New Hampshire, USA location! This role plays a crucial role in our ambitious journey to uphold and improve our world-class standards in life sciences. As a member of our dedicated Quality Control team, you will directly contribute to technology transfer, validation, deviation support, routine testing, and investigation projects. This role is crafted for someone who excels in a collaborative environment and is dedicated to scientific excellence. | 12/16/2024 |
| 1987 | Lilly Lebanon, IN Sr./Principal Scientist - QC Bachelor’s degree (4-yr College) in a science field related to the lab (e.g., Chemistry, Biology, Microbiology, etc.) Exp: 1+ years |
The Senior/Principal Scientist - QC is part of the Lilly Lebanon API Quality Control team and provides technical leadership and expertise in the development, implementation, and maintenance of Quality Control laboratory systems to the Lilly Lebanon API site throughout the start-up, implementation, and day to day operations. The Senior/Principal - QC performs accurate and timely testing of routine and some non-routine lab samples in accordance with appropriate GMP and safety guidelines. The Scientist completes second person verification of other’s results. The Scientist also participates in laboratory root cause investigations, equipment evaluations and qualifications, and some quality system improvement initiatives by executing well-defined protocols and procedures. The Scientist shares technical information and best practice within plant sites or group. In addition, the Senior/Principal - QC will provide technical support to QC operations as part of the organization’s off-hours support strategy. After onboarding, this role will require a Short-Term Assignment (STA) of up to 6 months at a Lilly manufacturing site outside of the United States. | 12/16/2024 |
| 1988 | Lilly Lebanon, IN Manufacturing Scientist - Lebanon API Manufacturing Master's Degree in STEM Discipline (Chemistry preferred) Exp: 1 year |
The Manufacturing Scientist is part of the TSMS (Technical Services/Manufacturing Science) team that provides the technical support required to achieve reliable and compliant manufacturing of API molecules. This role will be part of the Manufacturing Process Team for its respective area, providing daily oversight to ensure safe and reliable supply of medicines. The Manufacturing Scientist executes technical projects (experimental, modeling and/or production data analysis) to improve and optimize process control, yield, purity, and/or productivity. In addition, the manufacturing scientist should be capable and of setting up and executing a variety of experiments at laboratory scale and conducting research on manufactured product for process improvements and troubleshooting in the technical services and manufacturing sciences laboratory. | 12/16/2024 |
| 1989 | Lilly Lebanon, IN Sr./Principal Scientist - QC Bachelor’s degree (4-yr College) in a science field related to the lab (e.g., Biology or Microbiology) Exp: 1+ year |
The Scientist-QC is part of the Lilly Lebanon API Quality Control team and provides technical leadership and expertise in the development, implementation, and maintenance of Quality Control laboratory systems to the Lilly Lebanon API site throughout the start-up, implementation, and day to day operations. The Scientist-QC performs accurate and timely testing of routine and some non-routine lab samples in accordance with appropriate GMP and safety guidelines. The Scientist completes second person verification of other’s results. The Scientist also participates in laboratory root cause investigations, equipment evaluations and qualifications, and some quality system improvement initiatives by executing well-defined protocols and procedures. The Scientist shares technical information and best practice within plant sites or group. In addition, the Scientist-QC will provide technical support to QC operations as part of the organization’s off-hours support strategy. | 12/16/2024 |
| 1990 | Lilly Lebanon, IN Sr./Principal Associate - QA Computer Systems Bachelor’s degree in Computer Science, Engineering, Life Sciences, or a technology-related field Exp: 1+ years |
The Associate - Computer Systems Quality Assurance is responsible for oversite of computer system validation at the Eli Lilly Lebanon API Manufacturing facility. This role includes working with Automation, QC labs, and Tech@Lilly persons to develop validation strategies for the approach to computer system validation in compliance with corporate standards; consultation and interpretation on applying and right-sizing validation requirements; maintaining corporate and site computer systems standards and practices; participating in internal and external Regulatory agency inspections; conducting evaluations of internal or supplier quality practices; maintenance of inspectional readiness; and external benchmarking of computer system validation practices. | 12/16/2024 |
| 1991 | Lilly Indianapolis, IN Scientist – API Manufacturing Process Support Master's Degree in STEM Discipline (Chemistry preferred) Exp: 1 year |
The Manufacturing Scientist provides the technical support required to achieve the reliable and compliant manufacture of the Active Pharmaceutical Ingredient External Manufacturing (API EM) portfolio which includes raw materials, intermediates, enzymes and bulk drug substances. The API EM Manufacturing Scientist executes technical projects (experimental, modeling and/or production data analysis) to improve and optimize process control, yield, purity, and/or productivity. In addition, the manufacturing scientist should be capable and technically independent in setting up and executing a variety of experiments at the laboratory scale and conduct research on manufactured product for process improvements and troubleshooting in the technical services and manufacturing sciences laboratory. | 12/16/2024 |
| 1992 | Lilly Indianapolis, IN Engineer, Drug Product Development Master’s or bachelor’s degree in engineering or in related fields Exp: 0-5 years |
We are seeking highly motivated professionals with experience in developing and commercializing parenteral drug product through various stages of clinical development. If you are interested in building platforms for new and novel therapeutic modalities and interested in building and leading a strong group of scientists exploring new frontiers into formulation and drug delivery strategies, you should consider joining our diverse team. | 12/16/2024 |
| 1993 | Lilly Indianapolis, IN Engineer - Facilities/Maintenance Bachelor of Science degree (Preferably in Chemical or Mechanical Engineering) Exp: 1 year |
This position is responsible for establishing and maintaining the reliable operation and qualified state of FUME owned equipment and business processes within the plant. Duties will require collaboration with the outsourced Facilities Management (FM) and Project Management (PM) service provider, Lilly Engineering Tech Center, and A/E firm to ensure facilities/systems meet the requirements of the business. | 12/16/2024 |
| 1994 | LSI Solutions Victor, NY Senior Molding Engineer Bachelor of Science Degree in a related discipline Exp: 1-5 years |
The Molding Engineer at LSI SOLUTIONS® plays a crucial role in creating and overseeing thermoplastic injection molding processes, utilizing scientific injection molding principles. The Molding Engineer will leverage their expertise to ensure consistent part quality and optimal cycle times. Additionally, they will provide oversight and foster collaboration with internal resources and external suppliers to ensure the implementation of best practices throughout the organization. | 12/16/2024 |
| 1995 | LSI Solutions Victor, NY Process Validation Engineer I Bachelor’s Degree in an engineering, technical or manufacturing discipline. Exp: 0-3 years |
The Process Validation Engineer will develop and execute validations to ensure regulatory compliance to established internal and external standards related to released product or current production. The individual will support the writing of validation protocols and reports, along with the gathering and analysis of data. | 12/16/2024 |
| 1996 | LSI Solutions Victor, NY Regulatory Associate Bachelor or Master’s degree in a technical, regulatory, or life sciences discipline Exp: 0-2 years |
The Regulatory Associate applies her/his experience, knowledge, organization skills, and communication skills in a wide variety of tasks. Regulatory Associates provide regulatory feedback and guidance based on medical device regulations and standards to the company throughout the development cycle. Regulatory Associates monitor regulations, standards, policies, and guidance for new and current compliance requirements that may have impact to the company. They maintain technical documentation and help to implement change control at LSI. Regulatory Associates are assigned to work in one or more of the following areas: Domestic, European, Rest of World, Labeling, and/or Clinical & Post Market Surveillance. Regulatory Associates assigned to Clinical projects contribute to clinical evaluation, investigator brochures, post-market clinical follow-up, and post market surveillance. All Regulatory Associates will also maintain full Quality and Regulatory compliance with all standards that govern the design, development, manufacturing, and distribution of our medical devices. | 12/16/2024 |
| 1997 | LSI Solutions Victor, NY Mechanical Engineer - Design I Bachelor’s Degree or higher in Engineering or related technical discipline Exp: 0-2 years |
As a Mechanical Engineer - Design, you will help bring a future generation of LSI products to market. You will be part of a team to further improve our current products that are already available by iterating on the innovative design. Working in a cross functional team, you will take ownership of all things related to the form, fit, function, and feel of the product. Other tasks include, stack up analysis, failure analysis, improvements for manufacturability, communicating design intent and inspection requirements with 3D and 2D CAD, and other tasks. | 12/16/2024 |
| 1998 | Lumanity Boston, MA Research Associate Master’s degree in health-related field Exp: 1-3 years |
We are seeking a Research Associate to join our Patient-Centered Outcomes team within our wider HEOR business. This is an excellent opportunity for an individual who is interested in conducting academic-type, patient-centric research. As our Research Associate, you will interact with patients with various diseases to determine how their diseases impact their health-related quality of life. Ultimately the research you do with help inform the development of clinical outcome assessments for use in clinical trials. | 12/16/2024 |
| 1999 | Lumen Seattle, WA Associate Scientist I MS/MSc degree in biochemistry, cell biology, immunology, virology, or related field of study Exp: 0-2 years |
Lumen is seeking a highly motivated, innovative Associate Scientist to join our team. The Associate Scientist will work with and support scientists in the Biologics research and development team. The work will involve various projects at different stages of the pipeline. The individual is expected to develop, optimize, design and execute a broad range of cell culture-based experiments and assays, as well as prepare and maintain cell line stocks. The individual is also expected to follow established protocols to perform assays, record, analyze, and report results. The position requires the ability to work as a team member in a fast-paced environment, have strong organizational skills, and take meticulous records. Effective communication skills are crucial in coordinating with the relevant teams to meet milestones and deadlines and in raising quality or troubleshooting issues as they may arise. The position will need to provide status updates and present in group meetings and company-wide meetings. | 12/16/2024 |
| 2000 | Magnet Biomedicine Boston, MA Sr. RA/Associate Scientist; Biophysics/Biochemistry MS in biophysics, biochemistry, chemical biology, or a closely related discipline Exp: 1+ years |
As a Sr. Research Assistant or Associate Scientist on the Screening, Biophysics, and Biochemistry team at Magnet Biomedicine, you will play a critical role in designing, executing, and interpreting biophysical and biochemical assays to discover and characterize small molecule chemical inducers of protein-protein interactions. This position offers a unique opportunity to contribute to the development of Magnet’s platform and the development of next-generation TrueGlue therapeutics. The successful candidate will collaborate with a team of passionate scientists to achieve our goal of bringing new medicines to patients. | 12/16/2024 |
| 2001 | Mallinckrodt Fenton, MO Quality Tech III Bachelors Degree in science related field (Chemistry, Biology) Exp: 1-3 years |
Provides technical support at an elevated level by developing solutions to routine problems of limited scope and complexity. Depending on the laboratory area, will perform analysis on Raw Materials, Intermediates, In-Process, Finished Product, or Stability samples using established analytical methods. | 12/16/2024 |
| 2002 | Mallinckrodt Raleigh, NC Operations Quality Engineer II B.S. degree in Engineering Exp: 1-5 years |
The role provides support for the various elements of the Quality System, including but not limited to the following: Deviations (Exceptions), Supplier Quality, Product complaints, Internal Audits, OOS, CAPA, Annual Product Review, Process control, Change Control, Validation, and identification/ recommendations for continuous improvement opportunities (internal/external). The Quality Engineer applies the appropriate statistical tools to analyze data, identify root cause and develop corrective actions for effective problem resolution of moderate to difficult scope and complexity. | 12/16/2024 |
| 2003 | Mallinckrodt St. Louis, MO Chemical Process Engineer B.S Degree in engineering or a technical related field (i.e. biology, chemistry, etc.) Exp: 1-3 years |
The Chemical Process Engineer is the recognized technical leader for manufacturing processes and for the improvement of existing processes. Consistently seeks for and evaluates methods to improve overall customer satisfaction through improved manufacturing efficiencies. Serve as main point of contact for manufacturing processes in their area in regard to safety, quality, and continuous improvement activities. | 12/16/2024 |
| 2004 | Mariana Oncology Watertown, MA Quality Control Analyst I/II Bachelor’s degree or Master’s degree in Biochemistry, Chemistry or related discipline Exp: 0-2 years |
We are seeking an experienced Quality Control Analyst I/II to join Mariana’s Analytical Quality Control function. You will be responsible for supporting the release and stability testing of our clinical therapies produced in our GMP manufacturing suite in Watertown. This person will play a role in creating and maintaining the highest standard of excellence for our therapies to treat cancer patients. | 12/16/2024 |
| 2005 | Mariana Oncology Watertown, MA Sr. Research Associate or Scientist, Biology MS in Biology, Cellular or Molecular Biology, Genetics, or a related discipline Exp: 1-2+ years |
We are seeking an experienced Senior Research Associate, Biology or Scientist, Biology to join Mariana’s Biology organization, advancing personalized medicine and radiopharmaceuticals. You will work as part of the team that is responsible for the validation of new targets and executing preclinical studies to advance the development of the next generation of radiotherapeutics. | 12/16/2024 |
| 2006 | Mariana Oncology Watertown, MA Research Associate, Discovery Chemistry B.S. or M.S. in Chemistry Exp: 0-2+ years |
We are seeking a highly motivated and energetic Research Associate, Discovery Peptide Chemistry to join Mariana’s Chemistry organization. The successful candidate will be a contributor to our targeted oncology platform in a pre-clinical, fast-paced discovery research environment through the purification and characterization of peptides. They will also work closely with the Medicinal Chemistry and Biology teams to support our drug discovery portfolio. The role requires the candidate to maintain broad scientific knowledge of high-performance liquid chromatography to execute peptide purification and characterization. The role also requires the candidate to become familiar with peptide synthesis and perform other chemistry tasks to support drug discovery efforts. The candidate should be a creative individual with good communication and interpersonal skills, and a willingness to step outside of their comfort zone. | 12/16/2024 |
| 2007 | Indivior Raleigh, NC Environmental Monitoring Technician Bachelor’s degree in Chemistry, Microbiology, Biology or other related Science Exp: 1-3 years |
The purpose of the EM Technician I is to perform routine environmental monitoring to assess the viable and nonviable particulate levels within classified manufacturing rooms and support rooms. | 12/11/2024 |
| 2008 | Integer Brooklyn Park, MN Quality Engineer 1 Bachelor’s degree in a related field Exp: 0-3 years |
Adheres to Integer’s Values and all safety, environmental, security and quality requirements including, but not limited to: Quality Management Systems (QMS), Safety, Environmental and Security Management Systems, U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements. Independently evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. Performs work which involves conventional types of plans, investigations, surveys, structures, or equipment. Applies standard practices and techniques in specific situations, adjusts and correlates data. Recognizes discrepancies in results and follows operations through a series of related detailed steps or processes. Reviews test procedures and plans prior to implementation, conducts failure analysis and inspection on products, processes and materials. Investigates, develops and implements new process technologies of moderate scope. | 12/11/2024 |
| 2009 | Integra LifeSciences Plainsboro, NJ Manufacturing Engineer I Bachelor's degree in Engineering (Mechanical Engineering, Pharmaceutical Engineering, Chemical Engineering, Biomedical Engineering) Exp: 0-2 years |
The Manufacturing Engineer I will play a key role in the support of manufacturing operations, process scale–up, and manufacturing improvement activities. They will oversee projects to evaluate, analyze, and improve existing processes, support the development of new manufacturing processes, implement statistical process controls, analyze and trend existing process parameters, improve manufacturing yields, reduce scrap, and error proof manufacturing processes. | 12/11/2024 |
| 2010 | Integra LifeSciences Boston, MA Quality Engineer II - Design and Reliability Assurance (DRA) Master’s degree in science, Engineering (Biomedical or Mechanical) or related discipline Exp: 0-2 years |
The Quality Design and Reliability Assurance (DRA) Engineer II is responsible for the efficient and compliant support of New Product Development (NPD) and Sustaining/Remediation project(s) of varying scope and complexity in the Tissue Technology (TT) division, specifically the Boston/ Braintree site. The role contributes and supports the design and development of new and improved products. The (DRA) Engineer II will interact with external design and development partners, participating on cross-functional project teams through all phases of the product development process, and assisting the technical team with planning, executing, documenting, and communicating testing activities. The role works with Product Development, Project Management, Regulatory, Marketing and Medical Affairs. | 12/11/2024 |
| 2011 | Integrated DNA Technologies (IDT) Coralville, IA Research Scientist II, Applied Science in Therapeutic Oligonucleotides Master’s degree (in Biology, Genetics, Chemistry or a related life sciences field) Exp: 1+ years |
This position is part of the Applied Sciences for Therapeutic Oligonucleotides team in our Gene Writing and Editing Business Unit located in Coralville, Iowa and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things! Function as a scientist at the bench, under minimal supervision, reporting to a team or project lead and executing projects as part of IDT’s new Genomics Medicine Service offerings related to: off-target safety assessment for CRISPR-based editing systems, CRISPR guide RNA sequencing, and additional, custom projects associated with IDT’s Therapeutic Oligonucleotides business. Provide teamwide scientific support on all aspects of therapeutic oligonucleotides projects inclusive of lab work, project tracking and organization, data collection, data analysis, report generation, and data presentation. Plan and keep detailed experimental records in facilitating technology transfer of methods from R&D to the Gen Meds Services team; gain expertise in technologies to support further feasibility, development and validation of assays as well as propose ideas for broader use and application. Lend subject matter expertise to customer-specific oligo assessment of quality, performance, safety, etc. in cell-based, biochemical or analytical assays; assist in the definition of technical and experimental work plans related to on-going efforts to advance customer projects while supporting customer progress towards cGMP oligonucleotide synthesis. | 12/11/2024 |
| 2012 | Intelivation Tech Plymouth Meeting, PA Associate Product Development Engineer Bachelor’s Degree in Mechanical Engineering or Biomedical Engineering. Exp: 1+ years |
The Associate Product Development Engineer will be responsible for all engineering functions of their product lines. They will take products from concept through development and market introduction while following all aspects of Design Controls. The Engineer will be driven and self- motivated working towards on time market introductions. | 12/11/2024 |
| 2013 | Perceptive New Haven, CT Image Analyst I BS in a relevant field (e.g. engineering, physics, neuroscience, chemistry, or biology) Exp: 0-1 years |
The Image Analyst I performs analysis and quality control (QC) on imaging data and metadata. Image Analyst I personnel are responsible for quantitative results generated in an imaging study. Analysts will be trained on all assigned analysis pipelines. Following demonstration of proficiency, analysts will contribute toward QC and troubleshooting of complicated analysis cases. Image Analyst I staff are assigned to multiple projects where they will work under the supervision of the project’s lead analyst. Analysts may also be asked to contribute to other analysis-related duties (creation and editing of SOPs, ad-hoc efforts, etc.). | 12/11/2024 |
| 2014 | Medical Diagnostic Laboratories (MDL) Hamilton Township, NJ Lab Technician I Bachelor Degree in Biology, Chemistry, or related science field Exp: 9 months |
Medical Diagnostic Laboratories (MDL), a member of Genesis Biotechnology Group, is a CLIA certified clinical laboratory with multiple state licensing, specializing in state of the art, automated DNA based molecular analysis of a variety of chronic and infectious illnesses. MDL specializes and performs Polymerase Chain Reaction (PCR) with a larger menu of testing available in the field of infectious disease. Our main theme of research is in the field of Gynecology, Infectious Diseases, Infectious Arthritis, Tick-borne Diseases, Mycology, and Chronic Fatigue Syndrome (CFS). MDL is looking for a Laboratory Technician. The Laboratory Technician is responsible for printing labels and attaching requisitions to the corresponding specimens. | 12/11/2024 |
| 2015 | Iovance Biotherapeutics Philadelphia, PA Analytical Sciences & Technology Specialist II Bachelor’s degree in biology, Biochemistry, Microbiology, Chemistry, or related scientific field Exp: 1-3 years |
The Analytical Sciences & Technology Specialist II Specialist is accountable for the technical development of quality control methods and processes, method and instrument validations, and technical transfers related to Analytical and/or Microbiological quality control testing of products, raw materials, and packaging components at the site. This role is also responsible for operating and maintaining quality control instrumentation in compliance with cGMP/FDA regulations, Iovance standard operating procedures, and policies. Given the nature of the process, this role also necessitates expertise in quality control techniques, analytical instrumentation, sterility principles, and an understanding of radiation safety standards. | 12/11/2024 |
| 2016 | Iovance Biotherapeutics Philadelphia, PA Quality Control Analyst I, Microbiology Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Exp: 1 year |
The Quality Control Analyst will support quality control testing operations at Iovance’s Cell Therapy Center (iCTC). The quality control testing programs include in-process and final drug product microbial testing such as bioburden, endotoxin, gram stain, environmental monitoring, and sterility techniques. | 12/11/2024 |
| 2017 | Iovance Biotherapeutics Philadelphia, PA Quality Control Analyst I, Microbiology - Night Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Exp: 1-3 years |
The Quality Control Analyst I will support quality control testing operations at Iovance’s Cell Therapy Center (iCTC). The quality control testing programs include in-process and final drug product microbial testing such as bioburden, endotoxin, gram stain, environmental monitoring, and sterility techniques. | 12/11/2024 |
| 2018 | Iovance Biotherapeutics Philadelphia, PA Quality Control Specialist I, Compliance Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Exp: 1-3 years |
lovance Biotherapeutics is a growing, late-stage company focused on the development and commercialization of novel cancer immunotherapies. lovance is seeking an Investigator I, for the Quality Control Compliance team who will in advance and close QC related investigations. Strong technical writing skills are required. Experience in a CAR-T or TIL environment is a plus. The ideal candidate will have experience working in a GMP-regulated laboratory with experience in writing investigations. | 12/11/2024 |
| 2019 | Iovance Biotherapeutics Philadelphia, PA Quality Control Specialist II, Compliance Investigator Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Exp: 1-5 years |
The Quality Control Specialist II, Compliance Investigator will assist the Laboratory Manager in advancing and closing QC related investigations. Strong technical writing skills are required with flow cytometry and ELISA experience. Experience in a CAR-T or TIL environment is a plus. The ideal candidate will have experience working in a GMP-regulated laboratory with knowledge of writing investigations but is not required. The position will be on-site at the Philadelphia location. | 12/11/2024 |
| 2020 | IQVIA Indianapolis, IN Laboratory Assistant BS in chemistry, biology, or medical laboratory technology Exp: 6 months |
We are seeking a Laboratory Assistant to join IQVIA Laboratories at Indianapolis, IN. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. The Laboratory Assistant is responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. | 12/11/2024 |
| 2021 | IQVIA Indianapolis, IN Scientist, LCMS Bachelor’s Degree in applied/laboratory sciences Exp: 0-2 years |
We are seeking a Scientist, LCMS to join IQVIA Laboratories at Indianapolis, IN. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. The LCMS Scientist will be responsible for executing laboratory experiments accurately and contributing to the design of scientific procedures, supporting scientific discovery while adhering to Good Laboratory Practices (GLP). | 12/11/2024 |
| 2022 | IQVIA Ithaca, Ne Associate Scientist, Sample Preparation Bachelor’s Degree in a Life Sciences discipline required Exp: 6 months |
We are seeking a Associate Scientist, Sample Preparation to join IQVIA Laboratories at Ithaca, NY. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. The Associate Scientist, Sample Preparation will be responsible for routine sample preparation duties, troubleshooting experiments, and preparing solutions and reagents to support laboratory operations. | 12/11/2024 |
| 2023 | IQVIA Indianapolis, IN Laboratory Associate BSc in a chemical, physical, biological, or clinical laboratory science, medical laboratory technology, or cytotechnology Exp: 6 months |
We are seeking a Laboratory Associate to join IQVIA Laboratories at Indianapolis, IN. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As a Laboratory Associate, you will be responsible for performing routine analysis and laboratory testing procedures to ensure compliance with regulatory standards. | 12/11/2024 |
| 2024 | IQVIA Valencia, CA Lab Associate- Specialty Processing BS in chemistry, biology, or medical laboratory technology degree Exp: 6 months |
We are seeking a Laboratory Associate- Specialty Processing to join IQVIA laboratory business at Valencia, CA. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As a Laboratory Associate, you will be responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. | 12/11/2024 |
| 2025 | Johnson & Johnson Spring House, PA Associate Scientist, API Cell Therapy Process Development B.S. in Biological Sciences, Biomedical Engineering or Immunology Exp: 1-2 years |
We are looking for an energetic, highly motivated and collaborative Associate Scientist candidate with demonstrated expertise in cell therapy process development and process innovation. In this role, the successful candidate will be involved in process design, unit operation development, and parameter optimization studies resulting in the development of new production processes. The successful candidate will work as part of a cross-functional teams supporting pre-clinical and clinical programs, focused on autologous processes. | 12/11/2024 |
| 2026 | J-STAR Research Cranbury, NJ Research Scientist of Crystallization R&D MS or BS. in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related field with a focus on crystallization, solid-state chemistry, or m Exp: 1-5 years |
We are seeking a highly motivated and skilled Research Scientist to join our Crystallization R&D Department at Porton J-STAR. In this role, this position is responsible for leading group or contributing individually to conduct Solid Form Studies and pre-formulation will search for the right solid form and develop formulations to support preclinical and Phase I studies including PK, PD, efficacy, tox studies. This role is also responsible for Crystallization Process Development will develop crystallization processes to define and control final solid form of drug substances with desired solid-state attributes needed for optimum performance as well as drug intermediates for robust purification. The responsibilities of the position include, but are not necessarily limited to, the items listed below. | 12/11/2024 |
| 2027 | J-STAR Research Cranbury, NJ Research Scientist Master in Chemistry, Chemical Engineering, Pharmaceutical Chemistry, or Food Science required Exp: 1 year |
Pharmaceutical Ingredients (API), intermediates, impurities, starting material and excipients from drug substances and drug products. Analyze organic and inorganic compounds to determine chemical or physical properties, composition, structure, relationships, reactions, using chromatography, spectroscopy, spectrophotometry techniques including HPLC, UPLC, IC, GC, MS, UV,XRPD,DSC, TGA, NMR, and KF. Design and perform method verification and validation. Determine the specificity, linearity, accuracy, precision, forced degradation, robustness of the methods. Collect and analyze data, and maintain data integrity under GMP, GLP, and FDA regulations. Prepare documentation of test procedures and technical reports. Prepare, review, and/or approve methods, protocols, and development reports. Maintain laboratory instruments to ensure proper working order. Apply Scientific expertise to troubleshooting, laboratory investigation and problem resolution. Participate in maintaining high quality laboratory environment and comply with Health, Safety and Environmental responsibilities for the position. | 12/11/2024 |
| 2028 | J-STAR Research Cranbury, NJ Senior Research Scientist I/II, Analytical Development MS in Chemistry, Pharmaceutical Science or related field. Exp: 0-5 years |
J-STAR Research, Inc. operates as a contract research organization for pharmaceutical and biotechnology companies worldwide. It offers services in the areas of custom synthesis/contract research, process and analytical research, cGMP synthesis, crystallization process development, solid form screening and selection, pre/early formulation, and drug substance-drug product coprocessing. | 12/11/2024 |
| 2029 | J-STAR Research Cranbury, NJ Senior/Principal Scientist, Solid Form Selection/Preformulation Development MS in Chemistry, Pharmaceutical Science or related field. Exp: 0-5 years |
J-STAR Research, Inc. operates as a contract research organization for pharmaceutical and biotechnology companies worldwide. It offers services in the areas of custom synthesis/contract research, process and analytical research, cGMP synthesis, crystallization process development, solid form screening and selection, pre/early formulation, and drug substance-drug product coprocessing. | 12/11/2024 |
| 2030 | J-STAR Research Cranbury, NJ Analytical Research Scientist II/III (DPD) MS in Chemistry, Pharmaceutical Science or related field. Exp: 1-3 years |
The primary responsibility in this role is to perform analytical testing of drug substance, intermediates, drug product in support of J-Star’s drug product development projects. The incumbent should provide the expertise in characterization of drug product formulation using HPLC, GC, DSC, TGA, XRPD, dissolution apparatus, particle size analyzer, Karl Fischer titrator. Specifically, the incumbent will be responsible for analysis of formulations from preclinical through clinical formulation development, of oral solids, liquids, injectables and semi-solid dosage forms for new drug candidates. | 12/11/2024 |
| 2031 | J-STAR Research Cranbury, NJ Research Chemist MS degree in Chemistry, Chemical Engineering or related field Exp: 6 months |
Perform API crystallization process in compliance with cGMP and FDA regulations, utilizing analytical tools including chromatography, separation, and solvent selection; support crystallization process development by conducting studies involving compound properties and experimental conditions; participate in the scale-up development of enabling technology and experiments to facilitate the co-processing and development of API; conduct routine stability, performance, and evaluation studies for solid state characterization and pre-formulation support; support early drug crystallization process development for high potency compounds and controlled substance; purify pharmaceutical compounds using column chromatography, crystallization, trituration, extraction, and distillation; utilize experimental and simulation/modeling approaches to perform solvent selection and solve process challenges arisen from scale-up crystallization process; collect, analyze and maintain data integrity under Good Documentation Practice; write/review developmental chemistry, process optimization and process scale-up reports to support FDA requirements for CMC (Chemistry, Manufacturing and Control) sections of INDs/NDAs. | 12/11/2024 |
| 2032 | Jubilant Spokane, WA EM Specialist - Weekend Nights Bachelor degree with a major in Microbiology, Medical Technology or related science Exp: 1 year |
The Environmental Monitoring department performs the functions associated with sampling, initiating tests, collecting and evaluating test results related to defined quality parameters for surface, air, personnel, product and utility systems such as compressed gases and WFI. The Specialist oversees EM functions and personnel, schedules tasks and personnel, assists in training EM Technicians and gown training of all aseptic personnel. | 12/11/2024 |
| 2033 | Jubilant Spokane, WA QC Scientist I-III Bachelor of Science in Chemistry, Biology, or related hard science Exp: No exp |
The QC Scientist I/II/III performs the analysis on allergenic and client components, raw materials, intermediates, and finished products following written procedures, providing the data required to determine raw material, product disposition. In addition, this position demonstrates leadership, teamwork and technical expertise. | 12/11/2024 |
| 2034 | Jubilant Spokane, WA Validation Associate Bachelors of Science in technical or scientific discipline Exp: 1-2 years |
The Validation Associate works closely with the Validation Specialist in support of capital, contract, and compliance projects. This position is responsible for executing a variety of validation studies, including performance qualifications and/or requalifications for terminal and component sterilization work. | 12/11/2024 |
| 2035 | Jubilant Spokane, WA EM Specialist - Weekend Days Bachelor degree with a major in Microbiology, Medical Technology or related science Exp: 1 year |
The Environmental Monitoring department performs the functions associated with sampling, initiating tests, collecting and evaluating test results related to defined quality parameters for surface, air, personnel, product and utility systems such as compressed gases and WFI. The Specialist oversees EM functions and personnel, schedules tasks and personnel, assists in training EM Technicians and gown training of all aseptic personnel. | 12/11/2024 |
| 2036 | Jubilant Spokane, WA QC Microbiologist I-II Bachelor of Science in Microbiology or related hard science with microbiology emphasis Exp: No exp |
The QC Microbiologist I-II performs the microbial analysis on allergenic and client components, raw materials, intermediates, and finished products following written procedures, providing the data required to determine raw materials/product disposition. | 12/11/2024 |
| 2037 | Katalyst South Plainfield, NJ Quality Analyst Master’s degree in pharmacy, biotechnology, chemistry, biochemistry, chemical engineering, mechanical engineering, industrial engineering, biomedical Exp: 6 months |
Involve in the design, development, implementation, testing, documentation & support of cGxP systems as per 21 CFR Part 11 & US FDA. Responsible for qualification & validation (IQ/OQ/PQ), master plans, protocols, changes requests, gap & root cause analysis, risk management plans, traceability matrix, summary reports for facilities, equipment, systems & processes. Preparation, review, authorize & submission of documentation for quality compliance & regulatory authorities. | 12/11/2024 |
| 2038 | KBI Boulder, CO Process Development Associate I B.S. degree in microbiology, biochemistry, chemistry, engineering, or related area Exp: 0+ years |
The Process Development Associate supports and executes laboratory studies within the KBI Process Development organization at KBI under general supervision. The Process Development Associate is able to execute lab work, with documentation and reporting that is consistent with Process Development compliance and Quality standards. The Process Development Associate is able to author basic operational documents for routine unit operations within the laboratory organization. The Process Development Associate is capable of executing lab studies from written documents and applies standard scientific approaches to solving technical problems. The Process Development Associate may serve as the point of contact for a specific laboratory project. The Process Development Associate works under the general supervision of laboratory management with work reviewed for soundness and accuracy. | 12/11/2024 |
| 2039 | KBI Durham, NC Manufacturing Associate I - Downstream (Night Shift) Bachelor’s degree in a related scientific or engineering discipline Exp: 0-2 years |
The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Manufacturing Associate must follow written, approved procedures and forms to ensure all work is conducted “Right First Time” (RFT) following Good Manufacturing Practice (GMP), including good documentation practices, and/or Good Laboratory Practice (GLP). As needed, the Manufacturing Associate will work individually or on teams to author standard operating procedures (SOPs) or Master Batch Records (MBRs); write corrective and preventive actions (CAPAs); and specify, commission, and qualify new equipment. | 12/11/2024 |
| 2040 | KBI Boulder, CO Process Engineer I Bachelor’s degree in Engineering, Biotechnology, Biochemical Engineering, or a related discipline. Exp: 0-2 years |
We are seeking a motivated Engineer I to join our engineering team and provide support for the manufacturing equipment at our biopharmaceutical manufacturing facility. In this entry-level position, you will assist with the maintenance, troubleshooting, and optimization of key manufacturing equipment, including UFDF (Ultra-Filtration/Diafiltration) systems, Centrifuges, Homogenizers, Fermenters, and other process equipment. You will work closely with experienced engineers and cross-functional teams to ensure the efficient and compliant operation of the manufacturing systems, while adhering to cGMP (current Good Manufacturing Practices) and regulatory standards. | 12/11/2024 |
| 2041 | KBI Durham, NC Microbiology Associate II Master’s degree in Microbiology, Biology or related technological field of science. Exp: 1-3 years |
The Microbiology Associate will be part of the Microbiology Department responsible for the testing and support for the Microbiology Laboratory in support of a Contract Manufacturing biotechnology facility and Process Development. Responsibilities includes laboratory support, program testing, reporting of results, execution of protocols. | 12/11/2024 |
| 2042 | KBI Boulder, CO Research Analyst I B.A. or B.S. degree in chemistry, biochemistry or related are Exp: 0-2 years |
Analyst position in a growing team that supports a variety of testing in support of the manufacturing of biopharmaceutical products in a contract development and manufacturing space. | 12/11/2024 |
| 2043 | KBI Boulder, CO Research Associate I B.A. or B.S. degree in chemistry, biochemistry or related area Exp: 0-2 years |
Analyst position in a growing team that supports a variety of testing in support of the manufacturing of biopharmaceutical products in a contract development and manufacturing space. | 12/11/2024 |
| 2044 | KBI Durham, NC Validation Engineer l Bachelor’s degree in Chemical Engineering, Industrial Engineering, Biomolecular Engineering, Mechanical Engineering, or related scientific field. Exp: 1-3 years |
The Validation Engineer I/II will be responsible for facilitating the validation lifecycle process for the Validation Department to ensure all equipment and systems are in a qualified state suitable for the intended use. This may entail, assisting with the planning, development, project management, and execution of life cycle engineering and validation lifecycle documentation elements of engineering and validation lifecycle design, commissioning, maintenance, qualification, and the interfaces with quality system lifecycle compliance requirements. | 12/11/2024 |
| 2045 | Krystal Biotech Pittsburgh, PA Process Validation Associate Bachelors’ Degree in Chemical Engineering, Biomedical Engineering, or related Exp: 1+ year |
Krystal Biotech is seeking a highly motivated Process Validation Associate (1+ years’ experience) to support process validation planning, design, and execution. This person will be responsible for risk assessments, process improvements, investigations, and other projects. They will also play a pivotal role in technology transfer and ensuring processes transition properly from site to site. | 12/11/2024 |
| 2046 | Krystal Biotech Moon Township, PA Bioprocess Engineer Bachelor’s degree, preferably in life sciences Exp: 1+ years |
Krystal Biotech, Inc is seeking a highly motivated and dynamic Bioprocess Engineer to support our product manufacturing at our Pittsburgh GMP facility. This role is critical to our make a meaningful difference in the lives of underserved patient populations having rare diseases. Quality, safety and on-time delivery is a must to be successful in this role! The ideal candidate will have foundational experience in upstream and/or downstream biologics or gene therapy manufacturing. | 12/11/2024 |
| 2047 | Gilson Middleton, WI Electrical Engineer I Bachelor of Science degree in electrical engineering or a related science Exp: 1 year |
Responsible for the design and analysis of hardware and firmware integration for new products and modifications to existing products. Additional responsibilities may include some project management and the ability to work on cross-functional product development teams. Basic research may be done during early project feasibility studies or for new concept investigations. Assignments will be broad in nature, requiring initiative, originality, and ingenuity. | 12/05/2024 |
| 2048 | Globus Medical West Carrollton, OH Associate Engineer, Manufacturing Bachelor’s degree in an engineering discipline preferred Exp: No exp |
As an Assoicate Manufacturing Engineer, you will develop, implement and maintain methods, operation sequence, and processes in the manufacturing of parts, components, sub-assemblies, and final assemblies. Support new initiatives and productivity targets for given manufacturing processes. Responsibilities will also include participation in design reviews, design transfer to production as it relates to the development of manufacturing processes, post-processing development, equipment and process validations, process definition for machine operation and maintenance requirements, test/inspection methods, fixturing, gauging and applying inspection and process control techniques. | 12/05/2024 |
| 2049 | Glyphic Biotechnologies Berkeley, CA Scientist, Assay Development BS/MS in molecular biology, biochemistry, chemistry or related fields Exp: BS/MS with 2+/1+ (for Scientist I) |
We are seeking an experienced Assay Development scientist to conduct experiments that will enable the next generation of sensitive, accurate, and scalable single-molecule protein sequencing. The ideal candidate will thrive in a dynamic research team as part of an intellectually stimulating and collaborative project. As a scientist at our early-stage startup, the candidate will have an opportunity to apply their creativity, knowledge, and enthusiasm and make significant contributions to an exciting and impactful project. The scientist will report to Director of Assay Development and bring their expertise in molecular biology to a cross-functional project at the interface of molecular biology, chemistry, bioinformatics, and automation. This is a full-time, exempt, in-person role based in Berkeley, CA. | 12/05/2024 |
| 2050 | Gore Associates Flagstaff, AZ Industrial Engineer Bachelor’s degree in Industrial Engineering or degree in related disciplines Exp: 1 year |
We are looking for Industrial Engineers to join our manufacturing teams for multiple openings. You will be a member of a cross-functional team supporting commercialized medical device manufacturing. The industrial engineer’s responsibility will be to apply industrial engineering fundamentals and contribute to Lean process improvements, data analysis, cleanroom layout design, and demand and capacity plans. The ideal candidate will be passionate about providing Industrial Engineering support for state-of-the-art implantable medical devices, energized by working for a world-class manufacturer and collaborating on cross-functional teams, recognize the importance of building and maintaining strong interpersonal relationships and possess strong attention to detail, and excellent documentation skills. This position will be located at our facility in Flagstaff, Arizona, with the possibility of a hybrid remote work arrangement, depending upon the responsibilities of the role and business needs. | 12/05/2024 |
| 2051 | Grifols Vista, CA Manufacturing Technician I Bachelor’s degree Exp: 1-2 years |
The Manufacturing Technician I performs fundamental tasks within a GMP environment in support of more complex manufacturing operations. The Tasks include, but are not limited to, cleaning and maintaining the work place so that it meets the standards for controlling bioburden levels; cleaning operating equipment per applicable procedures so that it meets the standards established to prevent product contamination and maintaining records/logs neatly and accurately and in accordance with current standard procedures. The technician performs job tasks in a safe manner while following specific department safety rules. | 12/05/2024 |
| 2052 | Grifols San Francisco, CA Senior Research Associate Masters degree in Life Sciences or related discipline Exp: 1 year |
We are seeking a talented and highly motivated Senior Research Associate to support our diverse antibody therapeutics pipeline. This position will offer exposure to drug development, from early research through development/manufacturing, with ample opportunity to learn new methods, design experiments, and present your work. | 12/05/2024 |
| 2053 | Grifols San Diego, CA Research Associate 2 Molecular R&D B.A./B.S./M.S. Molecular Biology, Chemistry, Biochemistry or related field. Exp: 1-3 years |
Research Associate 2 is responsible for designing and performing experiments while collaborating and communicating effectively. | 12/05/2024 |
| 2054 | Grifols Research Triangle Park, NC Senior Associate Research Scientist I Masters in Biology, Biochemistry, Chemistry, or Toxicology Exp: 1 year |
This Senior Associate Research Scientist I position is in the CMC Development, Bioanalytics, Analytical Operations Group. The selected candidate will be responsible for conducting testing of process intermediates and final container in support of manufacturing, process development, developmental stability, validation and other R&D projects. Other responsibilities include cGXP documentation, sample login, data review, instrument maintenance and troubleshooting, data analysis, and other tasks assigned by management. The analyst may participate in development, execution, and qualification of new analytical test methods for characterization. The incumbent will be expected to work effectively under minimal supervision, and contribute to the team effort to support R&D projects. | 12/05/2024 |
| 2055 | Grifols Clayton, NC Assistant Biologist BS degree in biology, chemistry, or related field Exp: 6-12 months |
This position is responsible for performing environmental monitoring of fill lines in SFF and PFF and also environmental monitoring of all classified production areas, including sampling of site utility systems. Environmental Assurance department must maintain adequate staffing to support all filling operations 24 hours per day, 7 days a week. In addition to routine environmental monitoring of the aseptic fill lines, this position is also responsible for executing the Quality Oversight program for the fill lines and also provides quality control approval of air flow visualizations conducted on site. This position is part of the budgeted staff necessary to complete this sampling and testing and to ensure that Clayton site environmental monitoring of the aseptic fill lines and other production areas and utility systems remain in a state of control. Must be able to perform tasks by following SOP’s and oral instructions. Must have precise, legible, and organized documentation skills. Candidates must also be willing to perform ones share of cleaning duties and housekeeping. | 12/05/2024 |
| 2056 | Grifols Clayton, NC Automation Engineer I/II Master’s Degree - Engineering, Automation, Computer, Industrial, Manufacturing, Related Exp: 0-1 years |
The Automation Engineer I is an entry level professional who is responsible for using technology to improve and streamline a manufacturing process through automation. Depending on their specific assignment, this person provides automation support for projects or within a specific area, or provide validation support for automation projects. The Automation Engineer I can also integrate into a project team. The incumbent is knowledgeable in Automation with the capability to learn specific control systems, instrumentation, process, utilities, or qualification testing. He/she supports meeting customer needs and business goals. In addition, he/she will collaborate with other automation engineers. The Automation Engineer II is a junior level professional who is responsible for using technology to improve and streamline a manufacturing process through automation. Depending on their specific assignment, this person provides automation support for projects or within a specific area or provide validation support for automation projects. The Automation Engineer II will also integrate into supporting a large-scale project. He/she is recognized as proficient in their field such as specific control systems, instrumentation, process, utilities, or qualification testing. He/she meets customer needs in support of business goals. In addition, the incumbent will collaborate with other automation engineers. | 12/05/2024 |
| 2057 | Grifols Norfolk, VA Field Service Engineer Bachelor’s degree in Engineering, Technical or related Scientific Discipline Exp: 0-2 years |
The position will be responsible for customer relationship management and collaborating with interdepartmental teams to ensure proper resolution and close out of regulated documentation in the CRM system. The FSE will manage all preventative maintenance and system upgrades of instrumentation and its interface at the customer site and provide troubleshooting to diagnose and resolve technical issues on a variety of electromechanical, fluidic and medical devices . Deals with diverse and oftentimes complex issues where analysis may require in-depth evaluation of many factors, and functions as the reference for troubleshooting, investigations and log analysis for FSE team members within and outside the assigned region. The team is looking for an individual with first electrical / mechanical work experience. Independently exercises judgement in evaluating methods and determine criteria for obtaining solutions is a must. The FSE is required to live within 50mi of the Metro Atlanta area. | 12/05/2024 |
| 2058 | GSK Collegeville, PA Associate Scientist/Engineer – Sterile Process Engineering BS degree in Pharmaceutics, Biology, Biochemistry, Chemistry, Chemical Engineering, or related scientific discipline Exp: 1+ year |
Are you looking for a collaborative Associate Scientist role that allows you to contribute to designing innovative ways to use Engineering, Process Analytics Technologies, Automation and Modelling to develop medicines for patients? If so, this opportunity within the Sterile Process Engineering team would be the right fit for you. As an Associate Scientist you will join the Sterile Process Engineering and Analytics department of the Drug Product Development organization within the GSK R&D. You will primarily support drug product manufacturing process development using the small-scale capabilities, platform initiatives, combination product development, technology transfers, and new technology implementation for products in the pipeline. | 12/05/2024 |
| 2059 | Guardant Health Redwood City, CA Scientist I - Technology Development Bachelors or Masters Degree in Molecular Biology, Genetics, Biochemistry, or related field. Exp: 0-3 years |
The Technology Development Department is responsible for developing, validating, and implementing the tests used by Guardant Health for cancer detection. This role will be within the Product Development wing of Technology Development. The Product Development group is primarily responsible for late-stage assay development, including interfacing with early-stage assay development to finalize the assay, verifying and validating the product, and supporting transfer of the product to the Guardant health clinical laboratory and subsequent launch. The current focus of the role will be supporting regulatory submissions to both FDA and ex-US regulatory agencies as subject matter experts in analytical and clinical validation studies. However, the full scope additionally includes LDT and RUO product development and validation utilizing standard design control processes. | 12/05/2024 |
| 2060 | Guardant Health Redwood City, CA Biospecimen Associate I Bachelor of Arts or Science in Biomedical Laboratory Science, Clinical Science or related field Exp: 1-2 years |
The Biospecimen Associate I supports the management of patient samples and provides the link between the Clinical Operations and Client Services teams. The Biospecimen Associate I is responsible for receiving, unpacking, processing, and recording samples sent for laboratory testing under the supervision of the Biospecimen Management Supervisor. The Biospecimen Associate I has demonstrated an understanding of laboratory workflow. In addition to the primary role of biospecimen management, there may be a need to provide back-up support (non-testing) to the Analytical and/or Post-Analytical team. It is imperative that the Biospecimen Associate has demonstrated the ability to work independently, but also functions effectively as a member of the Guardant Health team. The nature of the work requires keeping organized records, excellent attention to detail, effective written and verbal communication skills, the ability to multi-task and be flexible with tasks and schedules, and the ability to work independently in a team environment. | 12/05/2024 |
| 2061 | FL106 (Flagship Pioneering) Cambridge, MA (Senior) Research Associate, Chemistry Bachelor’s degree in chemistry or a related field (e.g. organic chemistry, biochemistry, biotechnology or pharmaceutical science) Exp: 1+ years |
FL106 is seeking a highly motivated (Senior) Research Associate with expertise in chemistry to play a vital role in the company’s efforts to develop and validate novel target discovery approaches. The candidate must be independent, goal oriented, have excellent communication skills and be willing to work in a highly dynamic and fast-paced entrepreneurial environment. This is a unique opportunity to drive the growth of an early-stage biotechnology company where you can contribute to the next frontier of genetic medicines. We are looking for collaborative, enthusiastic problem-solvers to join our team, driven by a shared goal of making a practical impact. | 12/05/2024 |
| 2062 | FL106 (Flagship Pioneering) Cambridge, MA Senior) Research Associate, In Vitro, Cell and Molecular Biology Bachelor’s degree in Biology or a related field Exp: 1+ years |
FL106 is seeking a highly motivated (Senior) Research Associate with expertise in Cell and Molecular Biology to play a vital role in the company’s efforts to validate novel target discovery approaches. The candidate must be independent, goal oriented, have excellent communication skills and be willing to work in a highly dynamic and fast-paced entrepreneurial environment. This is a unique opportunity to drive the growth of an early-stage biotechnology company where you can contribute to the next frontier of genetic medicines. We are looking for collaborative, enthusiastic problem-solvers to join our team, driven by a shared goal of making a practical impact. | 12/05/2024 |
| 2063 | Heraeus Dayton, OH Quality Engineer Bachelors Degree in Chemistry or related field Exp: 1-2 years |
Facilitates the investigation and response to customer complaints and internal issues. Determine and eliminates root causes and diminish defect occurrences or quality incidents in the process. Supports the Quality Manager with internal and external audits, customer surveys, and respond or resolve corrective and/or preventive actions and verifications. Develops new approaches to solve problems identified during quality assurance activities. Supports the Quality Assurance group in streamlining Quality documentation. Communicates significant issues or developments identified during quality assurance activities and provides recommended process improvements to management. Documents data obtained during all quality assurance activities, consistent with company policies and procedures. Perform capability studies and statistical analysis using methods such as FMEA, GR&R, SPC, and SQC. Organize data from various sources into Excel for statistical analysis. Applies statistical analysis to investigate historical trends. Perform control charting and review prior to product shipment. Participate in pFMEA, Cpk, control plan; file and maintain related records. | 12/05/2024 |
| 2064 | Hesperos Orlando, FL Engineer Associate I Bachelor’s degree Exp: 1 year |
You are experienced in software development for scientific data and scientific equipment, and developing algorithms, software, and interfaces. You are conscientious and pay almost obsessive attention to detail, as organized documentation is second nature. You are curious, love learning, and are eager to take on hard problems. You thrive in a fast-paced environment and enjoy pushing the edge of what is possible. You are resourceful and like to work independently but are not shy to ask for advice. You are a cross-disciplinary team member, who is excited to work with and learn from other engineers, biologists, chemists, modelers, and experimentalists. You are comfortable communicating across teams. You deliver. You know that what matters is delivering a solution that works every time. | 12/05/2024 |
| 2065 | Biogen Research Triangle Park, NC Manufacturing Associate - Biologics Bachelor’s Degree (STEM preferred) Exp: Recent Grad/Entry Level |
Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; with two main areas/disciplines – Upstream (Cell Culture) and Downstream (Purification). MAs perform these critical steps within Current Good Manufacturing Practice (cGMP) biosafety cabinets and cleanroom suites. | 12/05/2024 |
| 2066 | Biogen Research Triangle Park, NC Manufacturing Associate IV Bachelor’s Degree (STEM preferred) Exp: 6 months |
Manufacturing Associates perform processing steps and manufacturing support activities in our facilities in Research Triangle Park (RTP). These teams are the backbone of our operations – each person playing a critical role in delivering our therapies to the patients who need them. This position will be in our Parenteral Filling operations, and our teams operate across the following units: Component Preparation, Compounding, Parenteral Filling/Lyophilization, Visual Inspection | 12/05/2024 |
| 2067 | Biogen Cambridge, MA Sr. Associate Scientist, DMPK In-Vivo MS degree in Pharmaceutical Sciences, Biochemistry, Chemistry, or a related field Exp: 0-2 years |
Biogen is seeking a highly motivated scientist to join the Drug Metabolism and Pharmacokinetics (DMPK) department at our Kendall Square site in Cambridge, Massachusetts. The role requires hands-on experience in conducting in-vivo studies in rodents, and basic familiarity with the concepts of pharmacokinetics (PK). The ideal candidate will not only conduct PK studies in nonclinical models but will also conduct animal surgeries when necessary. | 12/05/2024 |
| 2068 | HighRes Biosolutions Beverly, MA Mechanical Engineer/Document Control Specialist Bachelors degree in a relevant field of study Exp: Entry Level |
As a Document Control Specialist and Entry Level Mechanical Engineer at HighRes Biosolutions, you will work closely with engineering and operations to create, maintain, and check CAD and manufacturing documentation required to fabricate, build, and qualify our products. In addition, you will be a member of the mechanical engineering team, assisting in the design, development, testing, and maintenance of the HighRes hardware product catalog. The qualified candidate will have experience using SolidWorks and standard engineering drafting practices to document product designs. 50 – 60% of your time will be spent focused on document control with the remainder contributing to the work output by the mechanical engineering team. HighRes Biosolutions is a leader in the field of lab automation. Our mission is to improve human health through life science robotics, and we accomplish that through innovative software and hardware developed by a passionate team. Our systems and devices are used by the top pharmaceutical, biotech, and academic research labs throughout the world to help discover new drugs faster and more efficiently. In this role you will have a direct hand in helping deliver these lab automation solutions. | 12/05/2024 |
| 2069 | Hologic Newark, DE Supplier Quality Engineer Bachelor’s degree (BA or BS) from a university in Electronics or Mechanical Engineering or related Engineering field Exp: No exp |
Are you a detail-oriented and passionate engineer ready to kick-start your career in supplier quality? We are seeking a dynamic Supplier Quality Engineer to join our innovative team onsite in Newark, DE, supporting our Breast and Skeletal Health Division. This is an exciting opportunity to work closely with suppliers, ensure the highest quality standards, and make a significant impact on women's health. | 12/05/2024 |
| 2070 | Hologic San Diego, CA Systems Engineer 1 Bachelor's degree in Engineering (Mechanical, Electrical, Biomedical, or related field) or a Master's degree in a relevant field Exp: 6+ months |
We are seeking a motivated and detail-oriented Systems/Bioengineer to join our team. This role will involve working on the integration and automation of sample collection, nucleic acid extraction, and amplification processes for our innovative instrument platforms. The successful individual will be familiar with fixturing mechanical subcomponents and building breadboard systems. The instrument/subcomponents will utilize disposable parts. Therefore, the position requires basic knowledge in consumable molding, plastic sealing/welding, and amplification technologies such as PCR. | 12/05/2024 |
| 2071 | Hologic Marlborough, MA Manufacturing Engineer 1 Bachelors degree in Engineering or Science. Exp: 0-2 years |
Responsible for supporting medical device manufacturing engineering projects, processes, test and activities for Hologic’s product lines. Works with the manufacturing team and supports management goals for manufacturing activity aimed at providing cost efficient operations. To maintain engineering responsibility for the manufacture and performance of assigned product line(s). Participate in the transfer of design changes from design engineering to manufacturing. Performs root cause analysis and recommends corrective actions in response to manufacturing issues. Facilitate the transfer of major design changes that affect the product line. Communicate changes to manufacturing personnel. Assure that unique training requirements are met. Continuously support work to improve manufacturing methods, efficiency and product quality. Support the specification to provide the necessary tools, equipment, and fixtures for the assigned product line. | 12/05/2024 |
| 2072 | Hologic San Diego, CA Research Associate 1, Oncology B.A./B.S./M.S. in Biology, Biochemistry, Molecular Biology or related field Exp: B.A./B.S.: 1-2 years; M.S.: 0-1 years |
Biotheranostics, Inc., a Hologic company, is looking for an experienced research associate to join our oncology research and development team to strengthen our efforts in oncology diagnostic product development and research. Biotheranostics is a leader in the development of evidence-based biomarkers to address unmet medical needs and is experiencing dynamic and rapid growth. Its leading products are the Breast Cancer Index® (BCI) and CancerTYPE ID® (CTID). The company is based in San Diego, CA and offers testing services through its CLIA-certified, CAP-accredited laboratory. | 12/05/2024 |
| 2073 | ICON San Antonio, TX Laboratory Sample Processor (PRN) Bachelor’s degree Exp: 1 year |
We are currently seeking a Laboratory Assistant to join our diverse and dynamic team at ICON at our San Antonio TX site in a PRN (as needed) capacity. The Laboratory Assistant aids the technical staff with the handling and storing of and accounting for biological lab specimens, quality control and any other relevant tasks. | 12/05/2024 |
| 2074 | ICON Lenexa, KS Laboratory Assistant Bachelor’s degree Exp: 1 year |
If you have experience handling biological lab specimens and prepping samples for delivery to a clinical laboratory; learn how you can play a key role as Laboratory Assistant for ICON Laboratory Services which is dedicated exclusively to central laboratory testing and the associate services for clinical trials. | 12/05/2024 |
| 2075 | ICON Portland, OR Medical Technician I BSc or BA: Biology, Molecular Biology or Chemistry Exp: 1+ year |
This is an exciting opportunity to work within a fast-paced CLIA and CAP certified laboratory for a leading global provider of outsourced services to the pharmaceutical, biotechnology and medical device industries. Our Medical Technicians ensure the highest quality nucleic acid extractions, ensure timely storage of clinical samples, and perform general duties for the molecular laboratory, as directed. | 12/05/2024 |
| 2076 | Imperative Care Campbell, CA Manufacturing Engineer I Bachelor’s degree in engineering or related disciplin Exp: 0-2 years |
As a new professional in this field, this position will use acquired professional education and/or experience in mechanical, electrical, and/or pneumatic systems to focus on supporting activities related to the equipment used for manufacturing our company products. An individual in this role will be involved in drafting equipment installation/operation qualifications. This role will participate in the analysis of design studies to determine equipment capabilities, programs and solutions for increasing uptime that affect manufacturing processes. This hands-on engineering position will resolve issues related to calibration, preventive maintenance, and equipment repairs in accordance with maintenance schedules, manufacturer specifications, technical notices, equipment upgrades and safety issues. This position will address equipment related nonconformances and lead corrective and preventive actions. | 12/05/2024 |
| 2077 | INCOG BioPharma Fishers, IN Manufacturing Specialist BS in biological sciences/biotechnology Exp: 1 year |
INCOG BioPharma is seeking a highly motivated individual with subject matter expert (SME) capabilities in sterile pharmaceutical manufacturing process controls and industrial automation. The Manufacturing Specialist is a key technical role within INCOG BioPharma Operations. The ideal candidate must have experience in pharmaceuticals and/or biologics, GMP manufacturing, or within highly regulated industries. The Manufacturing Specialist’s primary responsibility is to efficiently and safely setup and operate various pieces of production equipment within the facility. They will be expected to work hands-on, be actively involved in continuous process improvements while taking ownership of the quality and quantity of product produced. The ideal candidate should possess a strong mechanical aptitude with strong trouble shooting skills on manufacturing equipment. They should demonstrate mentor and leadership skills to motivate manufacturing personnel, drive timely production activities and inspire problem solving & solution driven thinking. | 12/05/2024 |
| 2078 | INCOG BioPharma Fishers, IN Formulation Specialist BS in biological sciences/ biotechnology Exp: 1+ year |
The primary responsibility of the Manufacturing Specialist in Formulation is to weigh/dispense, setup/operate equipment to produce the bulk drug product for sterile manufacturing. They will be expected to work hands-on, be actively involved in continuous process improvements while taking ownership of the quality and quantity of product produced. The ideal candidate should demonstrate mentor and leadership skills to motivate manufacturing personnel, drive timely production activities and work effectively with internal partners, clients, and vendors. | 12/05/2024 |
| 2079 | INCOG BioPharma Fishers, IN MSAT Engineer Bachelor's degree in science or engineering Exp: 0-3 years |
The Manufacturing Science and Technology Engineer will be responsible for supporting all facets of tech transfer, process validation, GMP floor support, and continued process verification in accordance with current good manufacturing (cGMP) for clinical and commercial programs. This role will provide strong technical oversight to the business to ensure robust and reliable production processes are established. The MSAT Engineer is responsible for scaling up and transferring processes into full scale manufacturing process based on data generated internally or received from the client. | 12/05/2024 |
| 2080 | INCOG BioPharma Fishers, IN MSAT Engineer (2nd Shift) Bachelor’s or Master’s degree in science or engineering Exp: 0-2 years |
The Manufacturing Science and Technology Engineer will be responsible for supporting all facets of Tech transfer, Process Validation, GMP Floor Support, and Continued Process Verification in accordance with current good manufacturing (cGMP) for clinical and commercial programs. This role will provide strong technical oversight to the business to ensure robust and reliable production processes are established. The MSAT Engineer is responsible for scaling up and transferring processes into full scale manufacturing process based on data generated internally or received from the client. | 12/05/2024 |
| 2081 | INCOG BioPharma Fishers, IN Manufacturing Specialist- Formulation BS in biological sciences/ biotechnology Exp: 1+ year |
The primary responsibility of the Manufacturing Specialist in Formulation is to weigh/dispense, setup/operate equipment to produce the bulk drug product for sterile manufacturing. They will be expected to work hands-on, be actively involved in continuous process improvements while taking ownership of the quality and quantity of product produced. The ideal candidate should demonstrate mentor and leadership skills to motivate manufacturing personnel, drive timely production activities and work effectively with internal partners, clients, and vendors. | 12/05/2024 |
| 2082 | Incyte Wilmington, DE Research Scientist / Sr. Research Scientist, Cell Line Development Master’s degree in molecular or cell biology, chemical engineering, or related field. Exp: 1-3 years |
The Research Scientist/Senior Research Scientist in Cell Line Development will be responsible for the development of commercially viable cell lines that will be used in the production of therapeutic recombinant proteins such as fusion protein, monoclonal and bispecific antibodies. | 12/05/2024 |
| 2083 | Indee Labs Berkeley, CA MEMS Engineer Masters Exp: 1-3 years |
We are seeking an MEMS Engineer or Senior MEMS Engineer to join the team full time to accelerate the development of Hydropore in our Berkeley office. Indee Labs is headquartered in Berkeley, CA and accommodates remote work. This position will be located in Berkeley, CA and occasional work travel may be required. | 12/05/2024 |
| 2084 | Indee Labs Berkeley, CA Scientist, Immunology Masters Exp: 1-3 years |
We are seeking a Scientist or Senior Scientist, Immunology to join the team full time to accelerate the biological development of Hydropore at our Berkeley office. Indee Labs is headquartered in Berkeley, CA and accommodates remote work. This position will be located in Berkeley, CA and occasional work travel may be required. | 12/05/2024 |
| 2085 | Indee Labs Berkeley, CA Senior Bioengineer Masters Exp: 1-3 years |
We are seeking a Bioengineer or Senior Bioengineer, Immunology to join the team full time to accelerate the biological development of Hydropore at our Berkeley office. Indee Labs is headquartered in Berkeley, CA and accommodates remote work. This position will be located in Berkeley, CA and occasional work travel may be required. | 12/05/2024 |
| 2086 | Indica Labs Albuquerque, NM Integration Solutions Engineer Bachelor’s degree in computer science (CS), Computer Engineering (CE), Electrical Engineering (EE), Math or related. Exp: 1 year |
Indica Labs is looking for an experienced Integration Solutions Engineer. You will be responsible for configuring, optimizing, and maintaining integrations between various software systems and platforms, as well as managing integration projects and assisting with software installation and setup at client sites. | 12/05/2024 |
| 2087 | Evotec Seattle, WA Senior Associate Scientist Masters in biochemistry, chemistry, biophysics, chemical engineering, or related fields Exp: 0-1 years |
Just-Evotec Biologics is seeking an energetic, team-oriented scientist for a hands-on, laboratory based role supporting early and late stage drug product development including molecular assessment and formulation stability studies of antibodies, Fc-conjugates and other novel protein based molecules. The position requires experience with protein formulation development including stability study design and execution, data interpretation and cross functional team communication. The candidate should also have experience with analytical laboratory skills including chromatographic, electrophoretic, and spectroscopic techniques. The candidate must possess a strong ability to work as a team member while supporting multiple projects. Strong organizational, written, and verbal communication skills are necessary. The ideal candidate is efficient, curious, creative, enthusiastic, works well independently and in teams, and looks for ways to improve processes and technology. | 11/27/2024 |
| 2088 | Exactech Gainesville, FL Manufacturing Engineer Bachelor's degree Exp: 1-3 years |
Create and maintain the lowest cost, highest quality machining & manufacturing processes, tooling and supporting documentation for all parts produced. | 11/27/2024 |
| 2089 | Exelixis Alameda, CA QA Associate - Core Bachelor’s degree preferably in the life sciences or STEM disciplines Exp: 1-3 years |
The QA Core Associate supports QA Partner in GxP supplier quality management activities, vendor qualification, audit preparation, audit closure, audit observation tracking, vendor retirement, metrics collection, and records management. The position ensures data inputs in the Veeva supplier quality and audit modules and ensure audit logistics in regulatory and partner inspections. | 11/27/2024 |
| 2090 | Exelixis Alameda, CA Scientist II, Drug Substance Manufacturing BS/BA degree in chemistry, chemical engineering, life sciences or related discipline Exp: 1 year |
Responsible for the comprehensive review of documents and data analysis related to executed batch record packages, master batch records, protocols, reports, deviations, change controls, specifications, and risk assessments generated within the Commercial Drug Substance Manufacturing Group and related Contract Manufacturing Organizations (CMOs) to ensure compliance with all established and approved procedures. | 11/27/2024 |
| 2091 | Exelixis Alameda, CA Scientist II (Tumor Biology) MS/MA degree in related discipline Exp: 1 year |
The successful and highly motivated candidate will evaluate the activity of small molecule inhibitors in cell-based assays for oncology drug discovery. Comfortable in a dynamic and energetic team-based environment, the ideal candidate will actively contribute to develop cell-based functional assays and problem resolving, reliably execute experiments, interpret and analyze results. Good lab practicing and multitasking are required. This job will require the candidate to have good organization, communication and teamwork skills as well as flexibility and versatility to meet deadlines. | 11/27/2024 |
| 2092 | Bio-Techne San Marcos, CA Chemistry Associate Bachelor’s degree in Chemistry, Biochemistry, Biological Science, or related field Exp: 0-2 years |
Responsible for processing and formulation of controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for manufacturing quality products on schedule. General knowledge and basic application of concepts, theories, terminology and practices that apply to manufacturing in a laboratory environment. | 11/27/2024 |
| 2093 | Eyepoint Pharmaceuticals Watertown, MA Research Associate Bachelor degree in pharmaceutics or pharmaceutical sciences Exp: 1-3 years |
Eyepoint Pharmaceuticals is seeking a talented formulator to join our Development group in Watertown MA. Our department works closely with Operations and Regulatory affairs department to formulate and manufacture innovative ocular formulations. Ideal candidate should have a strong background in advanced physical chemistry, the use of polymers in Ocular Delivery. The selected scientist will design and conduct experiments to develop ocular formulations as well as to design and conduct robust analytical experiments for the designed formulations. The qualified candidate will interact with other departments, CMOs, participate in cross functional teams, contribute to the product development plans, and authorship of publications and pertinent sections of regulatory submissions, as needed. Additionally, the candidate must be a strong team player with excellent communication skills working in a complex cross-functional environment. The candidate must be able to work independently and take initiative by providing input on multiple projects. The candidate must be able to think critically, intellectually curious, and show resilience and courage to resolve complex formulation and manufacturing problems. | 11/27/2024 |
| 2094 | Eyepoint Pharmaceuticals Watertown, MA Process Engineer I Bachelor of Science, Engineering Exp: 1-2 years |
EyePoint is seeking a motivated Process Engineer I with excellent interpersonal skills to join our team. This person will be responsible for process sustaining and improvement of all components, device and packaging related projects. This position requires the application of continuous improvement, equipment oversight, trending, layout plans, testing, data analysis and report writing to resolve and improve manufacturing efficiencies. Candidate must be able to effectively collaborate with internal R&D, Quality, Regulatory and Operations departments and with external vendors and suppliers to deliver against project timelines and maintain process sustaining activities. The ideal candidate possesses the ability to develop credibility and trust as a technical resource to contribute to the company’s growth, productivity, and innovation. | 11/27/2024 |
| 2095 | Eyepoint Pharmaceuticals Watertown, MA Process Engineer I Bachelor of Science, Engineering Exp: 1-2 years |
EyePoint is seeking a motivated Process Engineer I with excellent interpersonal skills to join our team. This person will be responsible for process sustaining and improvement of all components, device and packaging related projects. This position requires the application of continuous improvement, equipment oversight, trending, layout plans, testing, data analysis and report writing to resolve and improve manufacturing efficiencies. Candidate must be able to effectively collaborate with internal R&D, Quality, Regulatory and Operations departments and with external vendors and suppliers to deliver against project timelines and maintain process sustaining activities. The ideal candidate possesses the ability to develop credibility and trust as a technical resource to contribute to the company’s growth, productivity, and innovation. | 11/27/2024 |
| 2096 | Flare Therapeutics Cambridge, MA Research Associate, Compound Management Bachelor’s degree in a relevant scientific discipline Exp: 0-3 years |
In this role you will Be responsible for managing Flare’s internal and external compound inventory using Mosaic SampleBank inventory system. Process and incorporate all new compounds into inventory using various liquid handlers. Collaborate with Medicinal Chemistry/Biochemistry/Biology/Proteomics/Translational Biology team members to provide support for fulfillment of dry/liquid compound requests and prepare custom assay ready plates. Utilize and troubleshoot various lab instrumentation such as Echo Acoustic Liquid Handlers, Plateloc, Janus, etc. | 11/27/2024 |
| 2097 | FlexDex Surgical Brighton, MI R&D Design Engineer Bachelor’s or Master’s degree in Mechanical Engineering, Biomedical Engineering, or equivalent Exp: 1-3 years |
To help realize our vision, we are looking to hire an experienced R&D Design Engineer with a strong background in product development, mechanical systems, and manufacturing. The candidate must have a strong understanding of processes related to design, prototype, testing, transfer of designs to manufacturing, V&V testing, and project management. In addition, experience and understanding of quality management systems is essential. | 11/27/2024 |
| 2098 | Fortrea Madison, WI On Call Clinical Research Technician Bachelor's in Science, preferred Exp: 1-2 years |
We are currently seeking a On Call Clinical Research Technician, to perform practical / administrative activities of clinical trials in Clinical Pharmacology in line with protocol and regulatory requirements. Many Clinical Research Technicians are drawn to their profession because of its direct impact on patient care. If this is your case, you will not miss that working in Phase 1 trials. Whilst allowing you to have a close face-to-face relationship with participants, and as you continue to practice your clinical skills and knowledge, you´ll be involved with the latest medical technologies and treatments, witnessing their development firsthand. When the drug you worked with gets approved, you know you´ll touch many patient´s lives around the world. | 11/27/2024 |
| 2099 | FMI Morrisville, NC Accessioning Technologist II Bachelor of Science degree in biological or life sciences Exp: 1-3+ years |
Accessioning Technologist II performs critical sample receipt and data entry functions in FMI’s CLIAcertified clinical laboratory. Specifically, the Accessioning Technologist receives all incoming samples and ensures that necessary information has been received to move forward with processing. This role is involved in both independent and collaborative work that includes the use of account or patient demographic data entry. | 11/27/2024 |
| 2100 | Fractal Therapeutics Atlanta, GA Chemical Engineer Bachelor of Chemical Engineering Exp: 1 year |
Chemical Engineer is needed in Atlanta, Georgia. Develop platforms to help clients in several pharmaceutical companies for drug development. Apply model-based techniques to improve preclinical and clinical R&D. Analyze and summarize complex pharmaceutics and PD datasets to investigate drug effects, and subsequently design the dosing strategies. Use fundamental principles to solve challenges in syntheses, process designs, and production. Develop computational fluid dynamics (CFD) models to solve the drying process in an agitated filter dryer (AFD), gas transportation in reactors, and tablet compression. Setup and perform simulations in LIGGGHTS (open-source DEM simulation software) for manufacturing of active pharmaceutical ingredients. | 11/27/2024 |
| 2101 | Fractyl Health Burlington, MA Clinical Trial Associate Bachelor’s degree in scientific field of study Exp: 1-3 years |
The Clinical Trial Associate will aid in study start up activities for Fractyl’s global clinical program, draft SSU documents, site regulatory document review and approval, and IRB/EC and regulatory submissions and approvals. Working closely with the clinical operations team members, the Clinical Trial Associate will liaise with internal and external partners to distribute continuous status updates. Main responsibilities include, but are not limited to, participating in the planning and coordination of clinical trial activities; providing project support for the initiation, execution and close out of clinical studies, working closely with internal teams and external vendors; and supporting project teams to achieve quality results in a cost‐effective and timely manner. | 11/27/2024 |
| 2102 | Fresenius Kabi Wilson, NC Associate Scientist B.S. in Chemistry, Biology or related physical science. Exp: 0-2 years |
An Associate Scientist is responsible for performing entry level chemical testing to support raw material, in-process, stability, and finished products as required for Quality Control. Effectively communicates work and results both orally and in writing. | 11/27/2024 |
| 2103 | Fresenius Kabi Wilson, NC Validation Engineer BS/BA degree in science, engineering, manufacturing technology or closely related field Exp: 1-3 years |
Responsible for providing technical support to operations in terms of equipment/system initial validation and equipment/system requalification’s. Will participate in equipment improvement teams charged with enhancing the compliance and performance of plant systems, while considering the regulatory requirements for change control. The individual must have a comprehensive understanding of cGMPs and become certified to enter Controlled Areas of the plant (Grade D, C and up to B/ A). The ability to write reports clearly, concisely and accurately; accurately record data and a basic understanding of statistical analysis is also required to perform these duties. Weekends and Off-shift hours are periodically required. | 11/27/2024 |
| 2104 | Freudenberg Carpinteria, CA Manufacturing Quality Engineer I Bachelor of Science Degree in Engineering or related field Exp: 0-3 years |
Participate in Measurement System Analysis activities including Gage RnR, Test Method Validations, Test Procedures, etc. as part of the Design Transfer process. Aid standardization initiatives for Quality Engineering at the site level and partners with other Freudenberg Medical facilities. Support and develop validation protocols and reports (IQ/OQ/PQ) and provide objective evidence that equipment, processes, test methods and product meet requirements and are compliant with applicable regulations. Uses statistical tools (Minitab, etc) to analyze data, make acceptance decisions, and improve process capability (Six Sigma, SPC, DOE). Assist Quality Engineering on MRB review of nonconforming products; recommends disposition and corrective actions. Performs complaint analysis investigations and trend reporting. Audit the Line’s production paperwork for accuracy; help drive the Line toward 100% first pass yield on DHR | 11/27/2024 |
| 2105 | Frontage Laboratories Secaucus, NJ Lab Technician BS in biology, chemistry, or related area Exp: 1 year |
The laboratory technician performs a variety of laboratory procedures as required by the study protocol. Laboratory technicians are responsible for assisting the Laboratory Manager, Principal Investigator, Clinical Research Coordinators, and other medical professionals in the preparation and handling of specimens, analyzing results, and maintaining laboratory equipment. Laboratory Technicians ensure accuracy, quality control, and adherence to safety protocols, contributing directly to scientific research, development of new products, or medical diagnostics. | 11/27/2024 |
| 2106 | Frontage Laboratories Exton, PA Scientist, Bioanalytical Services Master’s degree in Analytical Chemistry, Biochemistry, Pharmacology or related scientific discipline Exp: 1+ years |
Scientist / Bioanalytical Services Essential Functions Run sensitive, reliable and efficient LC-MS/MS bioanalytical assays for TK/PK assessment. | 11/27/2024 |
| 2107 | FUJIFILM Diosynth Biotechnologies Holly Springs, NC Sr. Analyst, QC Sample Control Master’s degree in science, preferably Chemistry, Biochemistry, Microbiology, Biology, or Life Sciences relevant scientific discipline Exp: 1 year |
The Sr. Analyst, QC Sample Control works independently with limited supervision and guidance from their manager to ensure all samples managed by the Sample Control team are handled and documented in accordance with applicable internal procedures. This role is responsible for handling samples manufactured at FDB Holly Springs, samples and reference materials from external sources, coordinating stability samples and protocols within the sample control team. This role is also responsible for coordinating with key internal stakeholders on the transport of QC samples from Holly Springs to external testing laboratories and support continuous improvement projects and SOP revisions by providing input into the sample handling process. A very high attention to detail and the ability to effectively communicate and function in a fast-paced, highly technical environment is essential to success. This role is included in routine on-call and weekend support, as needed. | 11/27/2024 |
| 2108 | FUJIFILM Diosynth Biotechnologies Thousand Oaks, CA Quality Control Associate Operations Bachelor’s degree Exp: 0-3 years |
The QC Associate Operations position is responsible for executing sample management activities, which include control, receipt, and distribution of product, intermediates, raw materials samples, sample retention, reference samples, and stability samples at Fujifilm Diosynth Biotechnologies California (FDBC). The QC Associate Operations position will interact regularly with internal QC, Quality Assurance, Manufacturing, Warehouse and Facilities groups. In addition to external Quality representatives supporting client requests and/or notifications. This position is expected to carry out all their activities in compliance with FDBC Quality processes, the requirements of the Quality Management System, and in compliance with regulation requirements governing laboratory controls and manufacturing. Individuals in this role are customer service-oriented, demonstrate fundamental awareness of verbal and written communication, problem solving, critical thinking, and time management. And role model company core values of trust, delighting our customers, Gemba, and Genki. | 11/27/2024 |
| 2109 | FUJIFILM Diosynth Biotechnologies Holly Springs, NC Sr. Analyst 1, QC Chemistry M.S. in Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field Exp: 1+ years |
The QC Chemistry Sr. Analyst 1 works with limited direction to execute QC analytical chemistry methods used in biological product manufacturing, including chromatography, spectroscopy, electrophoresis, wet chemistry, glycan analysis, sub-visible particle analysis, peptide mapping, and physical appearance, etc. The QC Chemistry Sr. Analyst 1 adheres to GMP-compliant laboratory operations in accordance with regulatory guidelines. This role generates analytical results and identifies laboratory exceptions, invalid assays, deviations, change controls, and corrective and preventative actions (CAPAs). The role is primarily responsible for executing routine analytical methods in support of manufacturing, supporting laboratory execution of analytical method transfers and validations, and training other QC Chemistry laboratory associates. The ability to effectively communicate and function in a fast-paced, highly technical environment is essential to success. | 11/27/2024 |
| 2110 | FUJIFILM Diosynth Biotechnologies Holly Springs, NC Sr. Specialist 1, QC Lab Support Master’s degree in science, preferably Chemistry, Biochemistry, Microbiology, Biology, or Life Sciences relevant scientific discipline Exp: 1 year |
Sr. Specialist 1, QC Lab Support works under moderate supervision, supporting and participating in QC activities related to investigations, deviations, OOS/OOT, CAPAs, and Change Controls. This role assists in creating and maintaining GMP documents and processes, collaborating with stakeholders and QA. This role contributes to customer contact and CLO communication to support QC capabilities in delivering materials and results. This role helps ensure QC compliance with policies and procedures. This role participates in project management and process improvement initiatives, developing skills in risk assessment. The role requires the ability to work effectively both independently and as part of a team, with growing cross-functional collaboration. | 11/27/2024 |
| 2111 | FUJIFILM Diosynth Biotechnologies Holly Springs, NC Process Engineer 2, Chromatography and Column Packing Master’s degree in Chemical or Biotechnology Engineering Exp: No exp |
This position reports to the Process Engineering Manager, Downstream in support of the Process Equipment team for the Aura project, a greenfield construction project in Holly Springs, NC. The initial assignment is to assume the Responsible Engineer role for Chromatography and Column Packing unit operations. As the site moves into commercial operations circa 2027, this position is planned to continue as primary support for Chromatography and Column Packing unit operations, with secondary responsibility expanding to cover additional Downstream unit operations includes supporting commercial operations, technology transfers, and small capital projects. | 11/27/2024 |
| 2112 | FUJIFILM Diosynth Biotechnologies Holly Springs, NC QA Analyst, PQS Bachelor’s Degree in Life Sciences (e.g., Engineering, Applied Science or Chemistry) Exp: No exp |
The QA Analyst, PQS assists in the quality oversight of PQS applications for the Enterprise Quality Systems administration and document control. The QA Analyst collaborates within the team as well as with other project teams on-site, and with QA departments at other FDB sites. This role focuses on consistent policy administration, assists QA oversight of daily activities, and resolves or mitigates issues that occur during operations. This role maintains relationships with site-based customers and global colleagues, and provide updates as requested. | 11/27/2024 |
| 2113 | FUJIFILM Diosynth Biotechnologies Thousand Oaks, CA Manufacturing Associate Bachelor of Science (B.Sc.) Exp: 0-3 years |
The Manufacturing Associate works as part of the manufacturing team to deliver high quality cell therapy materials during process transfers, routine production, and technology improvements. This position contributes to the successful delivery of released product in support of clinical trials and commercial production. | 11/27/2024 |
| 2114 | Galen Robotics Baltimore, MD Manufacturing/Sustaining Engineer Bachelor’s Degree in engineering Exp: 1-3 years |
The Manufacturing/Sustaining Engineer will focus on providing the highest level of engineering support for devices being developed and installed in the field and support ongoing sustaining engineering projects. Other daily responsibilities to include support of development team, contract manufactures along with providing support to R&D projects as requested. | 11/27/2024 |
| 2115 | GenEdit South SF, CA Research Associate, In Vivo Bachelor’s degree Exp: 1 year |
GenEdit is seeking a highly motivated and goal-oriented Research Associate with hands-on experience in performing in vivo studies to join our team. This full-time position will report to the Group Lead – In Vivo and will be responsible for testing nanoparticle encapsulated gene therapeutic drugs in vivo and related in vitro analysis of tissues and cells. Additional duties and responsibilities may be required as needed. The successful candidate will be a highly collaborative, resourceful, and effective team-player who is enthusiastic about tackling challenging complex scientific and technical problems with novel approaches and solutions. | 11/27/2024 |
| 2116 | Genezen Indianapolis, IN AD Lab Associate I/II BS or MS degree in Biology, Biochemistry, Molecular Biology, or similar field. Exp: 1-5 years |
We are looking for someone with high emotional intelligence and is comfortable working closely across the team to join us in facilitating the production of viral vectors. The Laboratory Associate I/II will be needed to perform analytical assays for viral vector process development, assist with method development, document experiments, help with lab maintenance and execute assay qualifications. This position calls for an independent thinker who can work seamlessly in a matrixed environment. | 11/27/2024 |
| 2117 | Genezen Lexington, MA Manufacturing Technician II BS degree in Life Sciences/Engineering Exp: 1+ years |
With general supervision the individual will perform routine and non-routine manufacturing operations, including but not limited to work functions in Cell Culture, Purification, Solution & Equipment Prep areas. Operates production equipment according to SOPs to produce clinical and/or commercial products. Independently perform manufacturing of Genezen’s therapeutic products and ensure this is realized and documented according to the highest industrial and GMP quality requirements This individual will carry out cGMP manufacturing operations utilizing Standard Operating Procedures (SOP), Batch Production Records and Solution prep records. | 11/27/2024 |
| 2118 | Genezen Lexington, MA Process Development Lab Technician B.S. degree in Biology, Biochemistry, Molecular Biology, or similar field Exp: 1+ years |
The Process Development Lab Technician will support the development and optimization of viral vector processes at Genezen’s Lexington site in MA. This role involves assisting with upstream and/or downstream process development activities, including cell culture, fermentation, purification, and formulation. The ideal candidate will demonstrate a strong enthusiasm for learning and developing new skills. This position requires a detail-oriented individual with the resilience to thrive in a fast-paced, dynamic environment and a commitment to maintaining high standards of safety and compliance. | 11/27/2024 |
| 2119 | Genezen Lexington, MA Process Engineer I, Manufacturing Sciences & Technology Bachelor's or Master's Degree in Engineering Exp: 0-3 years |
The Manufacturing Sciences & Technology (MSAT) group plays a critical role in successful manufacturing of clinical and commercial products. The person in this role assists the MSAT team in the transfer of technologies, process validation and cGMP manufacturing of Genezen’s gene therapy products. This individual will contribute as a core member of various cross-functional teams, and interacts extensively with other departments within Genezen including Process Development, Manufacturing, Engineering, Quality, and Regulatory Affair etc. | 11/27/2024 |
| 2120 | Genezen Lexington, MA Validation Engineer I/II Bachelor's Degree in Engineering Exp: 0-8 years |
The incumbent is responsible for assisting the Validation manager in completion of all project milestones. This includes installation, operational and performance qualification of equipment and utilities, environmental qualification, process validation, and preparation of all relevant documentation to meet regulatory requirements for new and existing products (includes standard operating procedures, technical reports and risk assessments). Duties require some knowledge in the pharma/biotech field. | 11/27/2024 |
| 2121 | GenScript Biotech Pennington, NJ QC Associate Scientist Bachelor’s degree in Molecular Biology, Biochemistry, Microbiology or related scientific field. Exp: 1-2 years |
The position reports to the Sr. QC Manager, is ideally suited for a professional with technical knowledge, and exposure to developing and carrying out processes, that are suitable for use in GMP manufacturing of a wide range of clinical trial materials, and participating in the technology transfer. There is a great opportunity to learn this function within a CDMO business, to support a broad portfolio and advance the manufacturing capabilities to deliver products to the client projects that transform the lives of patients. | 11/27/2024 |
| 2122 | GenScript Biotech Pennington, NJ Bioprocess Specialist-Upstream Processing Bachelor’s degree in science or engineering Exp: 0-5 years |
The Technician/Specialist, Bioprocess – Upstream Processing will work within the Upstream Processing group and performs the following activities while executing upstream operations: Preparation of stock solutions, buffers and media. Filtration of stock solutions, buffers and media. Set-up and operate disposable fermenters / bioreactors and other disposable bioprocess equipment including depth filtration. Passage and expansion of microbial and mammalian cell lines. The Technician/Specialist, Bioprocess – Upstream Processing supports relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate. | 11/27/2024 |
| 2123 | GenScript Biotech Pennington, NJ Bioprocess Specialist, Downstream Processing Bachelor’s degree in science or engineering Exp: 0-5 years |
The Bioprocess Specialist works within the Downstream Processing group. The Bioprocess Specialist will perform the following activities while executing downstream operations: Preparation of solutions, Filtration, Chromatography, Tangential flow filtration, Homogenizing, Drug substance formulation, Drug product formulation, Drug product vial filling. The incumbent works cross-functionally with internal departments and external resources on gene therapy manufacturing related issues. | 11/27/2024 |
| 2124 | Getinge Wayne, NJ Quality Engineer I Bachelor’s degree in engineering, Science, or other related field is required. Exp: 1 year |
As a Quality Engineer I specializing in Quality Operations, you will be responsible for overseeing and improving the quality of manufacturing processes, ensuring compliance with regulatory requirements, and driving continuous improvement initiatives to enhance product quality and customer satisfaction. You will play a key role in ensuring that our manufacturing operations meet the highest standards of quality and efficiency while adhering to relevant regulations and industry best practices. | 11/27/2024 |
| 2125 | GigaGen South SF, CA Senior Research Associate Masters degree in Life Sciences or related discipline Exp: 1 year |
We are seeking a talented and highly motivated Senior Research Associate to support our diverse antibody therapeutics pipeline. This position will offer exposure to drug development, from early research through development/manufacturing, with ample opportunity to learn new methods, design experiments, and present your work. | 11/27/2024 |
| 2126 | GigaGen South SF, CA Research Associate Bachelor’s degree in Life Sciences or related discipline Exp: 1+ year |
We are seeking a talented and highly motivated Research Associate to support our diverse antibody therapeutics pipeline. This position will offer exposure to drug development, from early research through development/manufacturing, with ample opportunity to learn new methods, design experiments, and present your work. | 11/27/2024 |
| 2127 | Gilead Foster City, CA Sr Research Associate Protein Therapeutics M.S. Exp: 0+ years |
The Molecular Assessment group within the Protein Therapeutics department is looking for a talented and motivated senior research associate to join our team. For this laboratory-based role, the successful candidate will be mainly responsible for generating high quality molecular assessment data for a variety of early-stage biologics candidates using analytical methods. If you are passionate about developing new biologics and eager to grow and learn in an exciting and fast-paced environment, we encourage you to apply for this job. | 11/20/2024 |
| 2128 | Gilead Foster City, CA Research Associate- In Vivo Pharmacology BS Exp: 0-2 years |
We are seeking a highly motivated Research Associate to join our Oncology in vivo pharmacology team. The selected candidate will be responsible for evaluating novel oncology therapeutics in pre-clinical mouse oncology models. Hands on experience with pre-clinical mouse models is required. The successful candidate will be responsible for designing, generating and communicating pharmacology data to support the progression of oncology research programs. Title will be commensurate with experience. | 11/20/2024 |
| 2129 | Gilead Foster City, CA Sr Research Associate I - Pre-Pivotal Biologics Analytical Operations M.S. Exp: 0 years |
Gilead Sciences (Foster City, CA) is seeking a talented and highly motivated Senior Research Associate I to join our Pre-Pivotal Biologics Analytical Operations group. Our collaborative and interdisciplinary development team utilizes state-of-the-art technologies and innovative methodologies to advance medicines into the clinic. S/he will have opportunities for career growth through acquisition of new skills, experiences, and professional relationships in a fast-paced and resource-rich environment. | 11/20/2024 |
| 2130 | Gilead Foster City, CA Senior Research Associate I–Pre-Pivotal Biologics Development M.S. Exp: 0+ years |
Gilead has an opportunity for an industry experienced level scientist in the Cell Line Development (CLD) group at our Foster City campus facility. We are seeking a highly motivated, team-oriented individual to design and execute experiments to support cell culture and clone development for our rapidly growing biologics pipeline. The successful candidate will also contribute to the overall strategy of new technology development projects. | 11/20/2024 |
| 2131 | CytoSorbents Princeton, NJ Process Operator/Production Associate Bachelor of Science degree with Science major Exp: 0 years |
CytoSorbents is seeking a Manufacturing/Production Associate to work 2nd shift (2:00 – 10:30 pm) in Princeton, NJ. The Manufacturing/Production Associate will perform GMP activities associated with producing, cleaning, and packaging of CytoSorb®, a unique blood purification medical device used to control deadly inflammation in life-threatening illnesses in the ICU and cardiac surgery. Come join us in saving lives! | 11/20/2024 |
| 2132 | Day Zero Diagnostics Boston, MA Laboratory Technician, Molecular Assay Development Bachelor's degree in a chemical, physical, biological, or clinical laboratory science Exp: 1 year |
The Laboratory Technician will play an essential role in the operational side of the lab as well, as directly performing experimentation as part of the research and development team. The Lab Technician will be responsible for maintaining materials, reagents, bacterial stocks, waste streams, and lab cleanliness. In addition, they will assist with experimentation; strictly adhering to lab SOPs in the processing of laboratory samples and recording and communicating their results. | 11/20/2024 |
| 2133 | Day Zero Diagnostics Boston, MA Laboratory Technician II, Sequencing Technologies Bachelor's degree in a chemical, physical, biological, or clinical laboratory science Exp: 1-2 years |
Day Zero Diagnostics is seeking a Laboratory Technician II to support the Sequencing Technologies team. This candidate is responsible for daily high-throughput sample processing, conducting DNA library preparation, quality control (QC) assessments, and whole-genome sequencing (WGS) on both short- and long-read platforms with minimal guidance. They will handle reagent preparation and project-specific inventory while strictly following SOPs, meticulously documenting processes and delivering high-quality, timely results. Located in DZD’s new, state-of-the-art facility in Watertown, MA, this role provides opportunities for developing skills surrounding training, logistics, and data analysis in addition to wet lab developmen | 11/20/2024 |
| 2134 | Mammotome Cincinnati, OH Service Engineer Bachelor’s Degree in an engineering discipline Exp: 1 year |
The Service Engineer for Mammotome is responsible for improving the post-purchase experience of clinicians supporting breast cancer patients. You will champion continuous improvement throughout service operations, be a key contributor to EU & APAC service projects, and serve as the technical expert on aftermarket support for Mammotome capital products. This position is part of the Aftermarket Service and Solutions team located in Blue Ash, Ohio and will be an ONSITE position. At Mammotome, our passion is driving innovative technologies that create efficiencies, while never forgetting that at the heart of every breast cancer journey is a patient. You will be a part of the Service Support team and report to the Sr Manager, Global Sales Operations and is responsible for customer issue to resolution process. If you thrive in a fast paced, supporting, and problem solving role and want to work to build a world-class technical service organization—read on. | 11/20/2024 |
| 2135 | Dexorgen Rockville, MD Biological Technician MS in Biology or Chemistry Exp: No exp |
Perform biological technician duties in helping biological scientists conduct laboratory tests and experiments. | 11/20/2024 |
| 2136 | Diacarta Pleasanton, CA Clinical Laboratory Assistant BS/BA in life science Exp: 0-1 years |
A CLA performs laboratory duties under the supervision of a licensed CLS. This position is for assisting the CLS and for sample processing, equipment operation and maintenance, and documents. | 11/20/2024 |
| 2137 | Diacarta Pleasanton, CA Research Associate BS degree in molecular biology or a related field Exp: 0-2 years |
DiaCarta is seeking a highly motivated, independent, and interactive Research Associate to join the R&D function in the company. The new team member will participate in R&D activities with the goal of developing and launching new qPCR, NGS, and branched DNA tests for IVD cancer diagnostics applications. The successful candidate will have outstanding attention to detail, enjoy working in a fast-paced multidisciplinary team environment, and have exceptional hands-on laboratory skills. DiaCarta is a rapidly growing company, so the candidate must be highly motivated and committed to launching their career in an innovative area of molecular diagnostics. This is a full-time role in Richmond, and you will be reporting to the Senior Scientist. | 11/20/2024 |
| 2138 | Diacarta Pleasanton, CA Manufacture Technician BS. degree in Molecular Biology, Cell Biology, Biotechnology or related field Exp: 1 year |
This position is a member of a fast-paced production team and will be responsible for the following tasks. Purchase raw materials from a vendor. Receive incoming materials and perform inspection and inventory recording. Production of DiaCarta IVD products to meet sales demands. Labeling of raw materials and finished goods. Perform calibration or preventative maintenance of the instrument. Participate in process improvement projects. Compliance with corporate quality systems. Other on-the-job assignments indicated by management | 11/20/2024 |
| 2139 | Difgen Pharmaceuticals Tamarac, FL Analyst, Microbiologist I B.S. or M.S. in microbiology or equivalent Exp: 1-2 years |
The QC Microbiologist I performs microbiological testing of DI water, intermediate/finished products, and environmental bio-burden. He/She maintains a functional and current GMP compliant microbiology laboratory. | 11/20/2024 |
| 2140 | Eurofins Tustin, CA Chemist I - VOA GCMS BS or BA in chemistry or related field Exp: 1+ years |
Eurofins Environment Testing Southwest - Tustin CA is searching for a VOA GCMS chemist to prepare and analyze environmental samples following EPA protocols in adherence with Eurofins Quality Assurance programs and SOP’s. | 11/20/2024 |
| 2141 | Eurofins Spring House, PA Bioanalytical Scientist B.S./B.A. in Molecular Biology, Immunology, Cell Biology, Biology, Biochemistry, Biology, or related biological science discipline Exp: 1 year |
Develop and qualify cell-based or ligand-binding based bioanalytical assays to support high priority biological and vaccine programs. Analyze samples using multiple platforms such as Luminex, MSD, ELISA, or cell-based assay. Assess acceptability of analytical result data using LIMS or other computer software. Basic data assembly and visualization using Excel, Spotfire, and/or GraphPad. Work according to established Standard Operating Procedures (SOPs) and regulatory guidance. Maintain accurate records of ongoing projects in adherence with regulated documentation standards. Assist in generation and review of reports and contribute to trouble shooting efforts. Collaborate and communicate within and across the working group. Work in a structured environment under direct to moderate supervision. Adhere to GLP regulations and safety requirements in BSL-2. | 11/20/2024 |
| 2142 | Eurofins Cary, NC PLM Analyst BS or BA in a closely related science Exp: 1-2 years |
The Analyst prepares and analyzes environmental samples according to scientific methodology in compliance with company Quality Assurance programs and SOP’s, and must be knowledgeable of both job-specific routine and complex analyses. The analyst validates and reviews data for accuracy, and uploads laboratory data into the LIMS that ultimately generates required reports to clients. Schedules sample workload according to due dates and sample hold times, and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation. | 11/20/2024 |
| 2143 | Eurofins Pasadena, TX PLM Analyst BS or BA in a closely related science Exp: 1-2 years |
The PLM Analyst prepares and analyzes environmental samples according to the required methodology and company compliance. As an analyst you will gain experience of both job-specific routine and complex analyses. The analyst team also validates and reviews data for accuracy, uploads laboratory data into the LIMS system, and ultimately will prepare and generate required reports to our clients. As a member of our analyst team you will also oversee sample scheduling and work to meet sample due dates and hold times. | 11/20/2024 |
| 2144 | Eurofins Fort Lauderdale, FL Asbestos Analyst Bachelors degree in Microbiology, Biology, Geology or a closely related science. Exp: 1-2 years |
The Analyst performs analysis of bulk samples for asbestos using polarized light microscopy. Analysis of non-culturable surface and air samples for fungi is a plus but not required. The analyst validates and reviews data for accuracy, and uploads laboratory data into the LIMS and reports to clients. Schedules sample workload according to due dates and sample hold times and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation. | 11/20/2024 |
| 2145 | Eurofins Rensselaer, NY Chemistry Data Review and Technical Writing Associate Bachelor's degree in life sciences (Chemistry or Biochemistry major) Exp: Entry Level |
Eurofins is seeking a self-motivated, adaptable, and positive individual who can work both independently and as part of a team in a client facing environment. The primary purpose of this position is to perform analysis of manufacturing data from chromatography and other purification processes. Investigations will be performed to identify root cause and path forward for any out of trend data. Presentations will then be created to provide recommendations for actions when necessary. Troubleshooting equipment and processes, maintaining clean orderly work spaces, and ensuring compliance are all responsibilities of this role. Completes laboratory documentation and reviews logbook data. Complies with all pertinent regulatory agency requirements and maintains inspection readiness. Occasional opportunities for preparation and operation of chromatographic systems for small scale lab experiments. After completion of the experiments, data and statistical analysis will be completed to understand relationships and impacts to processes | 11/20/2024 |
| 2146 | Eurofins Columbia, MO Scientist II - Bioassay Bachelor’s degree in relevant field such as chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related Exp: 1-3 years |
Eurofins BPT-Columbia is looking for a Scientist to join our growing Bioassay team located in Columbia, Missouri. The Scientist position is an intermediate-level professional position involved in somewhat complex day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). Responsibilities include completing work for research and development under CGMP and/or GLP guidelines for studies, documentation, etc. Assisting in conducting, monitoring and reporting studies to ensure data accuracy and report quality. Providing somewhat complex analytical work on projects and studies using a range of analytical techniques and instruments. Working with increasing independence on studies and assignments. | 11/20/2024 |
| 2147 | DNAe Carlsbad, CA Associate Scientist Master of Science in Biology or related Exp: 1 year |
Research and study cellular molecules to develop an infectious disease molecular assay with knowledge of real-time PCR and NGS workflows. Perform nucleic acid extraction from human sample including whole blood. Perform experiments and procedures in accordance with guidance from supervisor or from written protocols. Documenting, reporting, and presenting results of experiments and procedures. Following work instructions and SOPs, documenting procedures as required by ISO 13485 quality management systems. Assisting in maintaining laboratory supplies and equipment. | 11/20/2024 |
| 2148 | Dragonfly Therapeutics Waltham, MA Associate Scientist II/Sr. Associate Scientist M.Sc. in Biochemistry, Biochemical Engineering, Chemistry, or related discipline Exp: 1-4 years |
Dragonfly Therapeutics is seeking an Associate Scientist II / Senior Associate Scientist to join our team (Title commensurate with experience). Responsibilities include providing biophysical and biochemical characterization of our candidates to inform lead selection, performing developability assessments, interpreting and summarizing results, authoring technical reports, representing the Protein Sciences function on cross-functional teams. The candidate must be independent, goal-oriented, flexible, and able to work efficiently across multiple projects. We are searching for enthusiastic and innovative individuals with a keen eye for detail, who thrive in a fast-paced, entrepreneurial environment. | 11/20/2024 |
| 2149 | Eclipse Bioinnovations San Diego, CA RNA Platform Manager MSc in Molecular / Cell Biology or related discipline Exp: 1 year |
We are looking for an RNA Platform Manager to join our team to support eMERGE, our partnership platform for RNA-based medicine success. This is role will be responsible for developing and maintaining partnerships with academics, biotechs, and biopharmas that are developing the next generation of vaccines and therapies. You will work with our Marketing and Sales teams to identify new areas for growth and to present on our capabilities to potential partners. You will also work with our Core and Custom Solutions teams to draft project proposals and statements of work to ensure that each partnership is a success. The ideal candidate will be excellent at presenting, well-organized, and passionate about the power of RNA to revolutionize medicine. | 11/20/2024 |
| 2150 | eGenesis Greater Madison, WI Quality Control Microbiology Specialist B.S./M.S. in Life Sciences or related field Exp: 0-3 years |
eGenesis is seeking an innovative QC Microbiology Specialist to lead and provide the technical and strategic oversight of eGenesis’ environmental monitoring program. In this position you will be responsible for hands on environmental monitoring sampling, testing, reporting and trending of eGenesis’ two GMP manufacturing facilities (Greater Madison Area and Northwest Indiana). You will ensure activities are executed in a cGMP compliant manner and will work collaboratively on implementation and maintenance of our contamination control program. The ideal candidate will be independently motivated, a strong communicator and demonstrate proficiency in regulatory compliance. This position will be an onsite position in the Greater Madison Area. | 11/20/2024 |
| 2151 | Elektrofi Boston, MA Engineer III M.S. in Chemical, Biomedical, Materials, or Pharmaceutical Engineering, or a related engineering discipline Exp: 1 year |
Elektrofi is seeking a motivated individual to join our biotech company as an Engineer III to support process development of the novel Elektrofi formulation platform. The individual will join a growing, multidisciplinary team of scientists/engineers and industry professionals. | 11/20/2024 |
| 2152 | Elutia Silver Spring, MD Research & Development Engineer PhD in life sciences, chemistry, material sciences, biomedical engineering or related field Exp: 1-3 years |
The R&D Engineer at Elutia is responsible for designing and developing biological-based medical devices, specializing in drug/device combination products according to industry standards. This role encompasses overseeing the entire development process, from initial concept through to commercialization. The R&D Engineer leads prototype and pilot production, develops and executes test methods, and collaborates with cross-functional teams to advance Elutia’s product pipeline. They ensure seamless product development and facilitate tech transfer for successful clinical and commercial use by applying critical thinking skills to solve technical issues. Additionally, the R&D Engineer contributes to the intellectual property portfolio and ensures compliance with regulatory requirements to gain product approvals and support product lifecycle management. The successful candidate will work onsite at the Company’s Silver Spring, MD facility. | 11/20/2024 |
| 2153 | Emerald Cloud Laboratory Austin, TX Laboratory Operator I, II, & III Bachelor’s degree Exp: 1-3 years |
The demand for our service is growing, and to meet that demand, we are recruiting Lab Operators looking to explore opportunities in the biotech space and grow with our organization. Qualified candidates will receive comprehensive lab and safety training, allowing them the ability to run protocols in our Austin facility. These protocols are critical to sustaining the high-quality operations of the facility and provide experience working in ECL’s unique, process-driven lab environment with our integrated software tools. | 11/20/2024 |
| 2154 | Empirico Madison, WI Assistant Scientist - Drug Discovery Bachelor’s degree in Molecular Biology, Biochemistry or a related discipline Exp: 1 year |
Empirico, a clinical-stage biotechnology company that combines unmatched expertise in human genetics-driven target discovery with world-class capabilities in siRNA medicines, is looking for a talented scientist to join our Drug Discovery team and help advance our growing pipeline. This is an excellent opportunity to make meaningful contributions to the discovery and validation of novel therapeutic targets. You will work closely with other scientists that have a passion for finding new approaches toward the treatment and prevention of disease. Your responsibilities will include performing different bioanalytical assays intended to provide key study readouts around biodistribution, pharmacokinetics, and pharmacodynamic biomarkers. The ideal candidate will have experience in both protein- and nucleic acid-based assays, be highly organized, and enjoy working in a team environment. | 11/20/2024 |
| 2155 | Endo Rochester, MI Quality Associate Specialist, Product Release BA/BS degree in a related discipline Exp: 0-1 years |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. All incumbents are responsible for following applicable Division & Company policies and procedures. | 11/20/2024 |
| 2156 | Endo Rochester, MI Microbiologist II Master of Science degree in microbiology, biology or related field Exp: 1+ years |
The Microbiologist II performs Quality laboratory microbiological analyses of materials including water testing, finished product testing, raw material testing, and method validation. Supports laboratory investigations of moderate scope and complexity while abiding by GMPs and GLPs. Has working knowledge of, and stays current with, regulatory guidance and compendia relevant to laboratories and pharmaceutical manufacturing. | 11/20/2024 |
| 2157 | Endo Rochester, MI Process Engineer I MS degree in Engineering or Chemical Engineering Exp: 1+ years |
The Process Engineer I, with guidance, performs various duties related to optimization and analysis of production processes, new products, processes and technology transfers. Prepare and execute engineering study protocols, manufacturing and packaging experimental / feasibility study / validation batch records and protocols and complete interim and / or final summary reports for marketed and new products. Perform or assist on-site and site-change technical transfer, scale-up or scale-down factor evaluation, manufacturing / packaging process and equipment troubleshooting, and SOP preparation and review. | 11/20/2024 |
| 2158 | Endo Rochester, MI Chemist II, Quality Control Laboratory Master’s Degree in chemistry, chemical engineering or related field Exp: 1+ years |
The Chemist II, under general supervision, performs QC laboratory chemical analyses of raw materials, in-process materials, stability & finished products, and testing to support process validation. Detects, participates and reports on OOS/OOT/NOE and other investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. May train less senior staff. | 11/20/2024 |
| 2159 | Endotronix Naperville, IL Quality Engineer I - Failure Analysis BS in Engineering (prefer Electrical or Biomedical) Exp: 0-1 years |
As a Quality Engineer in Failure Analysis you will be responsible for supporting various elements of the Quality System such as Complaint investigations, Non-Conformance Investigations, and general failure analysis. | 11/20/2024 |
| 2160 | Endotronix Naperville, IL Technical Product Engineer I Bachelor's degree in Electrical, Computer Science, Biomedical, Mechanical, or Reliability Engineering Exp: 1-2 years |
The Technical Product Engineer will take the lead in troubleshooting advanced technical support issues in the field that are escalated by the customer support team. This will include the intake, investigation, documentation, and resolution of complaints and other field issues. Troubleshooting will include investigating failures, identifying root causes, and providing resolutions for the end user. The engineer will work closely with R&D and use data analysis tools (MATLAB, Python, Minitab etc.) to analyze field, vendor, and internal test data as an aid in the troubleshooting process. Acting as a technical lead, they will provide feedback to R&D and manufacturing which can be used to initiate corrective action and/or reliability improvements. | 11/20/2024 |
| 2161 | Endotronix Naperville, IL Manufacturing Engineer I BS in Electrical Engineering, Mechanical Engineering, Biomedical Engineering, Computer Engineering or equivalent. Exp: 0-3 years |
This Manufacturing Engineer I is primarily responsible for developing and controlling the manufacturing process for the Cordelia System and Cordella Pulmonary Artery Sensor System (Cor PASS). | 11/20/2024 |
| 2162 | Epigen Biosciences San Diego, CA Senior Research Associate/Research Associate - Chemistry MS/BS in synthetic organic chemistry or related field Exp: 1+ years |
Experience with modern synthetic organic chemistry, purification, and analysis is required. Experience with using ChemDraw/Reaxys/SciFinder. Performance of routine synthesis of heterocyclic compounds in milligram to multi-gram scale to support lead identification and optimization and record-keeping. Performance of purification of synthesized compounds using prep-TLC, silica gel/C18 column chromatography. Performance of and analyzing compounds using NMR spectra and LCMS. Performance of Microsoft Office tools such as Word, Excel, PowerPoint and Outlook. Good communication and presentation skills to effectively work with cross-functional groups with diverse background and interests. Strong attention to detail, excellent written and oral communication skills. Ability to work with a team of individuals to meet goals | 11/20/2024 |
| 2163 | Epigen Biosciences San Diego, CA Senior Research Associate/Research Associate - Biology MS/BS in biology or related field Exp: 1+ years |
Experience with cell culture and cell-based in vitro assays is required. Experience with the development and optimization of in vitro biological assays is required. Performance of routine assays to support lead identification and optimization. Performance of molecular biology techniques, such as Western blotting and transient transfection. Performance of data analysis, reporting and record keeping. Performance of Microsoft Office tools such as Word, Excel, PowerPoint and Outlook. Good communication and presentation skills to effectively work with cross-functional groups with diverse background and interests. Strong attention to detail, excellent written and oral communication skills. Ability to work with a team of individuals to meet goal. | 11/20/2024 |
| 2164 | Evonik Allentown, PA Lab Technician BS Exp: 1 year |
The position exists to support lab experimentation associated with the conceptualization, synthesis development and transfer of lab scale procedures to the engineering team for scale up development. The incumbent will be involved in lab operations including chemical synthesis, purification and analysis. The candidate will be required to function effectively independently and in work teams. The position is responsible for safe operation of their lab unit and thorough documentation of observations and results. The position exists to support lab experimentation associated with the conceptualization, synthesis development and transfer of lab scale procedures to the engineering team for scale up development. The incumbent will be involved in lab operations including chemical synthesis, purification and analysis. The candidate will be required to function effectively independently and in work teams. The position is responsible for safe operation of their lab unit and thorough documentation of observations and results. | 11/20/2024 |
| 2165 | Evonik Birmingham, AL Maintenance Quality Engineer Bachelor of Science Degree in an Engineering discipline, preferably Mechanical or Chemical or other stem related field Exp: 1-3 years |
This position will be the primary owner of Facilities department Quality programs, including management of change, deviation investigations, and implementation of corrective / preventive actions stemming from audits and quality-related incidents. As program owner, this position will be responsible for on-time closure of all Quality records, via both direct execution by this position and by assisting / coordinating other positions in the department with their assigned records. Additionally, this position serves as the technical lead on maintenance topics related to development-scale equipment such as reactors, homogenizers, etc. The Maintenance Quality Engineer will identify critical spare parts, develop maintenance work instructions for technicians to execute, and directly assist technicians with execution and troubleshooting. Finally, this position will help drive the desired “utilities as processes” mentality by tracking and reporting daily utility (steam, water, etc.) data, analyzing for outliers, and proposing improvement actions. | 11/20/2024 |
| 2166 | Evonik Birmingham, AL QC Associate Scientist Bachelor’s degree in Chemistry or other relevant science. Exp: 0-3 years |
The Quality Control Associate Scientist performs accurate and timely testing of routine lab samples in accordance with appropriate GMP and safety guidelines. The Scientist will also perform equipment qualifications and quality system improvement initiatives by executing well-defined protocols and procedures. | 11/20/2024 |
| 2167 | Nanoimaging Services San Diego, CA Account Manager, Nanoparticle Sales None Exp: 0 yrs |
Reporting to the Head of Nanoparticle Characterization Sales, this role will work closely with the scientific and operations teams to help provide high-quality cryo-TEM Nanoparticle Characterization services to our clients. Key responsibilities include generating proposals, managing purchase orders, logging client interactions in our CRM, and providing day-to-day account support to maintain strong client engagement. This role is ideal for someone eager to build experience in account management and collaborate within a high-performing team. | 11/14/24 |
| 2168 | Charles River Wayne, PA Technician II – Analytical Bachelor’s degree (B.S.) or equivalent in biochemistry, chemistry or related discipline. Exp: 1-3 years |
Perform routine analytical methods independently as specified in standard in-house SOPs, Client Test Methods and other written procedures. | 11/11/2024 |
| 2169 | Charles River Wayne, PA Technician II – BioPhysical Bachelor’s degree (B.S.) or equivalent in biochemistry, chemistry or related discipline. Exp: 1-3 years |
Perform routine biophysical methods independently as specified in standard in-house SOPs, Client Test Methods, and other written procedures. Under direct supervision, perform method development work as assigned. | 11/11/2024 |
| 2170 | Charles River Wayne, PA Technician I – Analytical Bachelor’s degree (B.S.) or equivalent in biochemistry, chemistry or related discipline. Exp: 0-2 years |
Under direct supervision, perform Routine analytical methods as specified in standard in-house SOPs Client Test Methods and other written procedures. | 11/11/2024 |
| 2171 | Charles River Wayne, PA Technician I – BioPhysical Bachelor’s degree (B.S.) or equivalent in biochemistry, chemistry or related discipline. Exp: 0-2 years |
Under direct supervision, perform biophysical methods as specified in standard in-house SOPs, Client Test Methods, and other written procedures. | 11/11/2024 |
| 2172 | Charles River Malvern, PA Technician II Mammalian Cell Banking Bachelor’s degree (B.A./B.S.) or equivalent in Biology or related discipline. Exp: 1-2 years |
Under direct supervision, responsible for performing basic daily laboratory and clean room tasks as they relate to the operations performed within the Manufacturing department, including mammalian cell banking and vaccine preparation activities, data analysis and writing client batch records and SOPs. | 11/11/2024 |
| 2173 | Charles River Wayne, PA Technician I Environmental Monitoring and Contamination Control Bachelor’s degree (B.S.) or equivalent in biology or related discipline Exp: 0-1 years |
Responsible for performing daily laboratory tasks as they relate to the Environmental Monitoring and Contamination Control Department. | 11/11/2024 |
| 2174 | Charles River South SF, CA Research Associate I B.S. or M.S. in biology or related field Exp: 1-2 years |
We are looking for a Research Associate I to join our Insourcing Solutions team located in South San Francisco, CA. Mammalian cell culturing, including media preparation, cell line maintenance, plating, and transfection. Molecular biology tasks including but not limited to molecular cloning, DNA/RNA extraction from animal tissue and cultured cells, basic immunofluorescence assays, DNA library construction, ELISA, PCR, qPCR, ddPCR and Western blotting. Confidently conducting and troubleshooting assays and experiments in a research production environment with guidance from management. Participate in group meetings and present collated data packages for feedback and review. Maintaining detailed notes of experimental results, participation, and presentation of results at team meetings. Assisting with laboratory housekeeping tasks, including receiving, maintaining, and cataloging constructs and reagents. Complying with all laboratory safety procedures. | 11/11/2024 |
| 2175 | ChemGenes Wilmington, MA Senior Research Support Associate B.S. degree in Biochemistry, Biology or related field Exp: 0-2 years |
Manufacture of synthetic DNA & RNA compounds. Assist with experiments supporting research in the synthesis of single-cell-barcoded beads, quality control of the synthesized beads, and performing experiments that include basic molecular biology techniques to sequencing experiments to validate and troubleshoot synthesis of DNA oligos to beads. Provide comprehensive technical support for scientists in the company; executing and optimizing ongoing experiments, analyzing results and designing follow-up experiments based on the results, and presenting findings and insights at group meetings. Evaluating research methods, procedures and techniques based on established objectives, conceiving and designing basic experimental protocols to ensure project completion in a timely fashion; recording and organizing data generated from the experiments in clear, concise, and assessable format; perform basic coding and statistical analyses; processing of in-vitro and in-vivo RNA for preparation of RNA-seq libraries for sequencing in Illumina platforms (Mi-Seq including Hi-seq and Next-seq). Experienced in techniques including but not limited to: running agarose gel, polyacrylamide gel electrophoresis, reverse transcription, quantitative PCR, fluorescent microscopy, flow cytometry; maintaining inventories of lab stocks. | 11/11/2024 |
| 2176 | ChemPacific Baltimore, MD Chemist Master’s degree in Chemistry or Organic Chemistry Exp: 1 year |
Perform multi-step organic synthesis in solution and/or solid support: Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps such as extraction, recrystallization, silica gel column chromatography and LC/MS purification; perform cGMP synthesis of pharmaceutical ingredients; and perform process development and scale-up for kilogram quantities; and clearly record and communicate results and challenges to coworkers/supervisor. Equipments and tolls used included NMR, UV, MS and IR, Reactor (from 50ml to 221 to 10000l), vacuum pump, water aspirator, condenser, rotavap, voltage transformer, chromatography columns, TLC monitor, lyophilizer, separation funnel and addition funnel. | 11/11/2024 |
| 2177 | Cipla Fall River, MA Quality Control Chemist Level 1 Bachelor's degree (BS or BA), in Chemistry, Biology, Pharmaceutical Sciences, or related field Exp: 0-3 years |
The job of the "Chemist" is simply described as an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory. The job itself may be further modified with respect to the department, group, etc., as exemplified in the "Department" on an individual assigned basis to a sometimes-specific testing group. The role may be further modified based upon individual education, training, experience, or a combination of all three. | 11/11/2024 |
| 2178 | Cipla Central Islip, NY QC Chemist III Master of Science Degree Chemistry, Pharmaceutical Sciences, or related field Exp: 1 year |
Perform analytical testing for Raw Materials, Finished and In-Process of Drug Substances and Products like Related Compounds, Assay, Content Uniformity, Dissolution, Blend Uniformity, Karl Fischer Titration, and other related Physical testing for the methods using instruments HPLC, UV/VIS, Dissolution (USP-I, II & III) and FTIR. Execute Method validations of Drug Substance and Drug Products including Related Compounds, Assay, Dissolution, Content Uniformity, Blend Uniformity as per ICH guidelines/USP /FDA requirements. Collaborative team player with excellent communication skills working in a highly dynamic, cross disciplinary environment. Develop efficient and selective analytical procedures and draft/review laboratory SOP’s. Identify discrepancies, initiate, and investigate OOS/OOT results. Perform timely and accurate peer review of analytical test results report/document in notebooks. Maintain QC lab related systems to ensure compliance with industry standards. | 11/11/2024 |
| 2179 | Cirtec Medical Brooklyn Park, MN Quality Systems Engineer I Bachelor’s Degree Exp: 0 years |
The Engineer, Quality Systems position will be responsible for ensuring operational adherence and compliance to Cirtec Medical’s Quality Management System (QMS) requirements. This role will be expected to provide input on, and contribute to, development and implementation of Quality System improvement strategies and approaches. | 11/11/2024 |
| 2180 | Clasp Therapeutics Rockville, MD Research Associate/Senior Research Associate; Antibody Discovery and Characterization BS/MS degree in biology, biochemistry, chemistry, genetics or related disciplines Exp: 0-2 years |
The Antibody Discovery and Characterization Research Associate is a key role in our discovery pipeline and an excellent opportunity for career development within a fast-paced, collaborative environment. You will help to lead the discovery and characterization of antibodies utilizing phage display libraries and optimizing biologic therapeutics towards developability and specificity. You will be a motivated, collaborative and innovative scientist with a proven ability to solve complex problems and manage successful technology transfer working with our internal analytical development and process development group, as well as CDMOs while helping to establish and build out the antibody/protein engineering group. This position offers a unique opportunity to bring automation and high throughput approaches to classical biochemical and molecular biology problems with the goal of discovering truly cancer-specific and life changing therapeutics. | 11/11/2024 |
| 2181 | CMIC Group Hoffman Estates, IL Research Analyst Bachelors in Chemistry, Food Science, Engineering, Food Technology or related field Exp: 1 year |
The Research Analyst will perform lab activities in accordance with applicable Methods, Plans, SOPs/SWPs, GLP regulatory guidelines and 21 CFR Part 11 as directed from Group Leader and Sr. Analysts. Conduct Bio-analysis validation and sample analysis independently. Conduct Pre-Study with minimal supervision. Utilize establish techniques to compile and analyze data. Document work and maintain study documentation and lab records. Provide direction and technical assistance to lesser-skilled team members. Assist with SOP/SWP preparation and other technical related documents including client communications. Perform other routine laboratory duties as deemed necessary. Maintain a safe environment. | 11/11/2024 |
| 2182 | Coastar Therapeutics San Diego, CA Research Associate II M.S. or B.S. degree Exp: 1- years |
Coastar Therapeutics is currently seeking a talented and highly motivated research associate with molecular biology background to join the multidisciplinary R&D team. The candidate will be responsible for designing and executing experiments in support of the biological membrane coated virus development. The candidate will also be involved in developing and validating collaborating projects to support Coastar’s fast-growing preclinical pipelines. The successful candidate must demonstrate broad and in-depth knowledge of molecular biology techniques. This is a full-time position reporting to the CSO and is located at our corporate headquarter in San Diego. | 11/11/2024 |
| 2183 | Compugen South SF, CA Research Lab Technician Bachelor’s degree in life sciences Exp: 3-6 months |
The research technician will support ex-vivo and in-vitro experiments, as a part of the functional validation of immunomodulatory molecules discovered by Compugen. The research work under the supervision of scientists will include expression studies in human and mouse tumor-infiltrating immune cells, and functional immune assays for elucidation of mode of action. | 11/11/2024 |
| 2184 | Concuir Los Angeles, CA Project Engineer I and II BS Engineering degree required, Chemical, Mechanical or Biomedical Exp: 1-3+ years |
As a full-time employee of Concuir, Inc, you will provide consulting services to pharmaceutical, biotech and/or medical device manufacturing clients. In this role, you will quickly learn common client practices, recommend and implement improvements to reach project goals, and have the opportunity to scale-up and bring new products into manufacturing. You will be able to utilize your experience as well as benefit from Concuir’s portfolio of project management and cGxP best practices to drive your overall success. Projects range from design through qualification of production equipment, utilities modification, implementation of new facilities and process scale ups. | 11/11/2024 |
| 2185 | Confluent Medical Technologies Laguna Niguel, CA Process Development Engineer I BS degree in engineering Exp: 0-3 years |
Confluent Medical Technologies is dedicated to working collaboratively with our customers, taking their projects from rapid prototype into high volume production. Our unparalleled technical expertise, proven experience and partnership with our clients has allowed us to perfect the process necessary to deliver world-class medical devices through innovative material science, engineering, and manufacturing. Our primary capabilities include: Nitinol components, balloon expandable stents and balloon catheters, delivery systems, biomedical textiles, access kits, and guidewires. We take pride in our position as the leader in the medical technology space and are driven by a passion to create products that our clients have envisioned for their customers. We are looking for a Process Development Engineer I to join our Laguna Niguel, CA team. | 11/11/2024 |
| 2186 | Contract Pharmacal Corp Hauppauge, NY Chemist; Quality Control Bachelor’s degree in a science related field Exp: 1-9 years |
The Chemist is responsible for and has experience in performing chemical analysis for one of the assigned QC laboratories (Raw Material, Finished Product, Microbiology, ICP, Technical Support) which is responsible for the analysis and disposition of commercial materials (raw materials, finished product release, stability, validation, investigation), and environmental samples, as assigned, and documenting results in accordance with SOPs. | 11/11/2024 |
| 2187 | Contract Pharmacal Corp Hauppauge, NY Scientist I; Analytical R&D Bachelor’s or Master’s degree in chemistry or analytical chemistry Exp: 1-2 years |
Design and conduct routine laboratory analysis using various analytical instruments and software such as HPLC, UPLC, ICP, and UV-Vis. | 11/11/2024 |
| 2188 | Cook Medical Bloomington, IN Senior Material Scientist Master of Science degree in Materials Science or Polymer Science Exp: 1 year |
Support pre/post-market engineering by solving material problems to develop and improve medical devices and manufacturing processes and advance the strategic goals of the company. | 11/11/2024 |
| 2189 | Cook Medical Bloomington, IN Senior Material Scientist Master of Science degree in Materials Science or Polymer Science Exp: 1 year |
Support pre/post-market engineering by solving material problems to develop and improve medical devices and manufacturing processes and advance the strategic goals of the company. | 11/11/2024 |
| 2190 | CooperSurgical Tucson, AZ Technician I - Stem Cell Processing Tissue Bachelors in Laboratory Science Exp: 1 year |
Process cord blood and cord tissue samples at all workstations trained and maintain certifications. Adhere to guidelines set forth by the CBR Safety Program, understand job hazard analysis concerns, and communicate safety issues to the applicable Safety Representative. Communicate deviations from procedures, anomalies, and abnormalities to responsible parties (Supervisor, Management, Department, etc.). Perform all assigned duties in compliance with internal policies, processes and Standard Operating Procedures (SOPs) as well as external regulations as determined by regulatory agencies. Responsible for remaining current in all training. Perform repetitive tasks while maintaining attention to detail. Audit, verify, and maintain accurate records for each sample. Maintain donor, client, and employee confidentiality. Evaluate disposables and equipment for non-conformities and notify responsible parties (QC, Supervisor, and/or Management). Perform daily department startup /shutdown checklist tasks and documentation. Perform general lab cleaning and maintenance. Participate in department projects as needed. | 11/11/2024 |
| 2191 | CooperSurgical Portland, OR Laboratory Technician I Bachelor's degree in Science Exp: 1-2 years |
Maintains demonstrated proficiency with all applicable Standard Operating Procedures. Performs semen evaluations to screen, process, and preserve for future clinical use. Execute an array of laboratory procedures. | 11/11/2024 |
| 2192 | CooperSurgical Boston, MA Laboratory Technician I Bachelor's degree in Science Exp: 1-2 years |
Maintains demonstrated proficiency with all applicable Standard Operating Procedures. Performs semen evaluations to screen, process, and preserve for future clinical use. Execute an array of laboratory procedures. | 11/11/2024 |
| 2193 | CooperSurgical Livingston, NJ Laboratory Technician I Bachelor’s or Master’s Degree in Biology or other related science Exp: 1 year |
Performs complex molecular-based procedures on clinical samples with a high degree of quality and in accordance with standard operating procedures. Analyzes clinical results and provides diagnoses. Communicates and collaborates with other professionals within the company and clients, as needed. Properly uses and maintains laboratory equipment. Performs clerical tasks associated with clinical cases, including but not limited to: maintenance of specimen and case logs, preparation/documentation of assay worksheets, preparation of analysis sheets and clinical reports. Receives and verifies clinical samples. Witnesses hands-on clinical procedures. Participates in lab maintenance (i.e. cleaning, annual/bi-annual/monthly maintenance of equipment, unpack supplies, etc.). Complies with Safety Standards and Good Lab Practices. Performs additional duties or assignments as directed by management | 11/11/2024 |
| 2194 | CooperSurgical Tucson, AZ Technician II - Stem Cell Processing Tissue Bachelors in Laboratory Science Exp: 1 year |
Process cord blood and cord tissue samples at all workstations trained and maintain certifications. Adhere to guidelines set forth by the CBR Safety Program, understand job hazard analysis concerns, and communicate safety issues to the applicable Safety Representative. Communicate deviations from procedures, anomalies, and abnormalities to responsible parties (Supervisor, Management, Department, etc.). Perform all assigned duties in compliance with internal policies, processes and Standard Operating Procedures (SOPs) as well as external regulations as determined by regulatory agencies. Responsible for remaining current in all training. Perform repetitive tasks while maintaining attention to detail. Audit, verify, and maintain accurate records for each sample. Maintain donor, client, and employee confidentiality. Evaluate disposables and equipment for non-conformities and notify responsible parties (QC, Supervisor, and/or Management). Perform daily department startup /shutdown checklist tasks and documentation. Perform general lab cleaning and maintenance. Participate in department projects as needed. | 11/11/2024 |
| 2195 | CooperSurgical Cambridge, MA Laboratory Technician I Bachelor's degree in Science Exp: 1-2 years |
Executes an array of SOPs to screen, process, and preserve semen samples for future clinical use. This position is part of a dynamic laboratory system that includes primarily lab bench work and cryogenic procedures. This position works with multiple cross functional teams to achieve the best possible outcomes for the populations we serve. | 11/11/2024 |
| 2196 | CooperSurgical Los Angeles, CA Laboratory Technician 1 Bachelor's degree in Science Exp: 1-2 years |
Maintains demonstrated proficiency with all applicable Standard Operating Procedures. Performs semen evaluations to screen, process, and preserve for future clinical use. Execute an array of laboratory procedures. | 11/11/2024 |
| 2197 | Corcept Redwood City, CA Clinical Trial Assistant I BA/BS Exp: 0-5 years |
The Clinical Trial Assistant will assist the study team in ensuring the most effective and efficient conduct of clinical research projects by providing planning, implementation, and tracking support. | 11/11/2024 |
| 2198 | Corden Pharma Boulder, CO QC Analyst - Days Bachelor's Degree (BA) Exp: 1 year |
Performs all technician tasks accurately and efficiently without supervision. Initiates expert technical advice to customers and completes all tasks in the Technician Training manual. Maintains a high level of housekeeping and attention to detail. | 11/11/2024 |
| 2199 | Corden Pharma Boulder, CO QC Analyst - Nights Bachelor's Degree (BA) Exp: 1 year |
Performs all technician tasks accurately and efficiently without supervision. Initiates expert technical advice to customers and completes all tasks in the Technician Training manual. Maintains a high level of housekeeping and attention to detail. | 11/11/2024 |
| 2200 | Cresilon Brooklyn, NY Production Technician I, 2nd Shift Bachelors Degree Exp: 0+ years |
The Production Technician I is responsible for the aseptic manufacturing of Cresilon’s products for the animal health industry. The Production Technician II will be trained in clean room operations, aseptic techniques, and must demonstrate the ability to successfully pass gowning qualifications. The position involves operating simple and complex processing equipment, routine sanitization of cleanroom facilities, and manual cleaning of equipment. The ideal candidate will have a proven track record of steady progress in a similar manufacturing environment and must possess a willingness to learn all equipment and jobs in the assigned manufacturing and sanitation of clean room facilities as required. Production Technicians are also responsible for the quality of products produced by ensuring compliance with local, State and Federal regulations, including current Good Manufacturing Practices (cGMP). | 11/11/2024 |
| 2201 | Crystal Pharmatech Cranbury, NJ Associate Research Scientist / Research Scientist – Solid State and Pre-formulation B.Sc. or M. Sc. degree in Chemistry, Pharmaceutical Science, or related field. Exp: 1 year |
The Associate Research Scientist will report directly to a Senior Research Scientist and handle all areas of solid-state research applied to API and early formulation development. This includes crystal form screening, single crystal growth, early formulation development, and all aspects of physicochemical characterization. The candidate will develop experimental designs and must actively communicate across multiple functional areas. | 11/11/2024 |
| 2202 | CSBio Menlo Park, CA Chemist, Quality Control Bachelor’s in chemical engineering or chemistry Exp: 1 year |
CSBio is a peptide contract manufacturing founded in 1993. Our initial products were a complete line of automated synthesizers for manufacturing and process development, with a focus on cGMP production. In 1994, we opened our custom peptide facility and began producing high quality compounds for research organizations and pharmaceutical companies worldwide. In 2004, we opened our peptide production facility in Menlo Park, CA and in 2014, we expanded our production capability through the addition of a new, state of the art building dedicated to cGMP peptide production. In 2017, we passed a FDA inspection and were recommended to be approved for commercial drug substance manufacturing. In 2023, we added additional cGMP clinical production capacity in Milpitas, CA. | 11/11/2024 |
| 2203 | CSL Miami, FL Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 11/11/2024 |
| 2204 | CSL Kankakee, IL Senior Automation Engineer, Process Recipe Owner Bachelor of Science in an Engineering or other Science discipline Exp: 1 year |
Primarily accountable for the implementation, life-cycle management, and ownership of process recipes. These recipes and associated S-88 based library objects leverage a batch manager for execution and integration to MES functions. This single recipe design philosophy is referred to as Recipe Driven Execution (RDE). | 11/11/2024 |
| 2205 | CSL Springfield, IL Quality Specialist Bachelor’s degree in biological sciences Exp: 1 year |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 11/11/2024 |
| 2206 | Curia Rensselaer, NY Quality Assurance Specialist I Bachelor’s degree in Life Science or related field Exp: 0-3 years |
The Quality Assurance (QA) Specialist I is responsible for maintaining Quality databases and providing an on-the-floor QA presence and oversight to manufacturing operations. This position’s role will include identifying compliance risks in the operation prior to and during execution, avoiding deviation whenever possible as well as managing immediate corrective action such that a) adherence to cGMPs and internal procedures/policies are maintained, and b) appropriate immediate corrective action is implemented and effectively documented in order to provide traceability and substantiation of any claims to be made in the investigation. This position primarily works in the cGMP production areas to manage adherence to the quality system and to initiate and assist in the initiation and resolution of deviations. | 11/11/2024 |
| 2207 | Curium Maryland Heights, MO Quality Control Technician Bachelor Degree in life science or a related field Exp: 1+ years |
Perform assigned laboratory testing and related quality control activities in order to ensure compliance with applicable SOP's and cGMPs. Provide timely testing and notification of any aberrant occurrence to Management/Supervision that presents potential negative impact to manufactured or marketed product. | 11/11/2024 |
| 2208 | Perceptive New Haven, CT Chemistry Lab Technologist M.S. or B.S in a related field Exp: 1-3 years |
The role is responsible for the manufacturing of radiopharmaceuticals, conducting analytical techniques to evaluate made products and providing support to other teams within the Clinical Chemistry department. | 11/04/2024 |
| 2209 | Perceptive Needham, MA Laboratory Technician B.S. or B.A. in scientific discipline Exp: 1 year |
This position will have primary responsibility for maintaining lab cleanliness; assisting with managing hazardous and non-hazardous waste streams; receiving, distributing, and notifying other lab staff of incoming shipments. Additionally, this position may support Facilities and Lab Management staff with light equipment and facility maintenance, maintaining consumable supply inventory, and assist in managing our lab/office recycling. Other clerical and project support duties may be assigned as well. | 11/04/2024 |
| 2210 | Cambrex Longmont, CO Scientist I/II (Materials Characterization) BS Degree or MS Degree in Chemistry or related discipline Exp: 1-5 years |
As a Scientist within our Materials Characterization department, you will execute analytical methods and provide general analytical support, such as release and stability testing of drug substances and drug products. | 11/04/2024 |
| 2211 | Cambrex Marlborough, MA Clean Room Analyst - Microbiological Environmental Monitoring Bachelor’s degree or higher in Microbiology or related field Exp: 1 year |
Our Clean Room Services team is looking for both entry level and veteran Environmental Monitoring Analysts that are passionate about leveraging their talents to provide an outstanding customer experience. If you’re interested in receiving excellent training and working as part of a team of experts with opportunities for growth, you’ll be a great fit in our strong company culture. As a Cleanroom Services Analyst you will perform environmental monitoring and cleanroom qualifications within controlled environments. You will travel to regional client sites to provide your expertise with equipment, procedures, policies and regulations to ensure that their cleanrooms meet the requirements for safe manufacturing of medical devices, pharmaceuticals and other patient products. | 11/04/2024 |
| 2212 | Cambrex Charles City, IA Process Engineer I BS in Chemical Engineering Exp: 1-5 years |
The Process Engineer will be responsible for implementation of projects for the manufacture of APIs and bulk intermediates and other products from development through piloting and/or commercial production. | 11/04/2024 |
| 2213 | Biosearch Technologies Petaluma, CA Oligo Production Tech I/ II - Synthesis Bachelor’s degree in chemistry, biology, or a similar discipline Exp: 0-4 years |
The Diagnostic Oligo Production Tech I/II-Synthesis will perform tasks associated with the synthesis of RUO and diagnostic-grade oligonucleotides in a fast-paced, high-throughput manufacturing environment. To perform this job successfully, an individual must be able to satisfactorily perform each of the following essential functions. | 11/04/2024 |
| 2214 | Biosearch Technologies Petaluma, CA Oligonucleotide Production Technician - Synthesis Bachelors or Master's Degree in Life Sciences Exp: 0-2 years |
The Oligonucleotide Production Technician I – Synthesis will perform tasks associated with the production of modified oligonucleotides in a high throughput, fast paced, and time sensitive manufacturing environment. This position focuses within the Oligonucleotide synthesis department. An Oligonucleotide Production Technician I – Synthesis can be called on to work in any production shift in the Oligo Production Department. | 11/04/2024 |
| 2215 | Biosearch Technologies Petaluma, CA Chemistry Technician I / II -Solid Support Production Bachelor’s Degree in a Physical Science Exp: 0-2 years |
This role is responsible for the manufacturing of Controlled Pored Glass (CPG) materials by following established and robust protocols. This position will primarily work with solid phase chemistry that is used in oligo manufacturing. CPG material manufacturing includes amine and nucleoside modification of native CPG at various angstrom sizes as well as modification with proprietary dyes and quenchers. The Chemistry Technician I will also be responsible for the upkeep of basic CPG equipment used in these processes. | 11/04/2024 |
| 2216 | CAMP4 Cambridge, MA Associate Scientist, Oligonucleotide Chemistry MS in chemistry or related field Exp: 1-3 years |
CAMP4 is seeking a passionate and innovative researcher to join our Chemistry team. The candidate will contribute to CAMP4’s growing in-house oligonucleotide chemistry capabilities. This is a laboratory-based role and the successful candidate will bring expertise of oligonucleotide purification and analysis to advance our antisense oligonucleotide (ASO) drugs. Reporting to a Senior Scientist, the successful candidate will be self-driven and flexible with enthusiasm for contributing in a high efficiency and fast-paced environment with the ability to adapt to changing priorities. This position will be based in our Cambridge, MA location. | 11/04/2024 |
| 2217 | Abbott Sylmar, CA Technical Services Engineer I Bachelors Degree - (Preferred Electrical Engineering, Biomedical Engineering ) Exp: 0-2+ years |
Functioning under general supervision, provides independent clinical and technical support in response to inquiries from physicians, health care professionals, patients and field staff using professional knowledge and judgment. This level of the Technical Service Engineer (TSE) provides the clinical and technical interface between the medical community and various departments through consultation. Requires the application of theoretical principles and creative/analytical techniques typically acquired in a recognized four-year or more biomedical engineering or other medical-related academic course of study. Identifies and routinely uses the most effective, cost efficient and best practices to execute processes; continually evaluates their effectiveness and appropriateness. Stays abreast of and consults on technical advancements. Promotes the process of continuous quality improvement and risk management, and coordinates solutions for technical and project issues. | 11/04/2024 |
| 2218 | CareDx Brisbane, CA Manufacturing & QC Associate I BA/BS in Biological or Life Sciences Exp: 0-3 years |
The Manufacturing & QC Associate I will be an integral part of the Lab Services team, responsible for producing high-quality reagents to support patient testing in our Clinical Lab. This role includes participation in routine manufacturing and process development activities and provides support in troubleshooting and process improvement efforts. The Manufacturing & QC Associate I reports directly to the Supervisor, Manufacturing & QC. This is a full-time onsite position based in our Brisbane, CA Clinical Lab. | 11/04/2024 |
| 2219 | ZEISS Remote, IA Field Support Engineer I BS degree in Electronics, Engineering, Computer Technology and related fields Exp: 0-3 years |
As a Field Support Engineer I, you get to work with an astonishing team that plays a vital role in Ophthalmic Diagnostic repair and maintenance. The Field Support Engineer I, under close supervision and direction, installs, repairs, upgrades and performs preventative maintenance on specified Carl Zeiss Meditec instrumentation in a designated field service territory. Represents Carl Zeiss Meditec at customer locations and works to achieve a high level of customer satisfaction. Maintains all company property (inventory, tools, diagnostic equipment, vehicle, etc.) in accordance with company policies. Maintains a high level of professional communication with team, customers, management, Sales and Technical Support. | 11/04/2024 |
| 2220 | ZEISS Remote, MN Field Support Engineer I BS degree in Electronics, Engineering, Computer Technology and related fields Exp: 0-3 years |
As a Field Support Engineer I, you get to work with an astonishing team that plays a vital role in Ophthalmic Diagnostic repair and maintenance. The Field Support Engineer I, under close supervision and direction, installs, repairs, upgrades and performs preventative maintenance on specified Carl Zeiss Meditec instrumentation in a designated field service territory. Represents Carl Zeiss Meditec at customer locations and works to achieve a high level of customer satisfaction. Maintains all company property (inventory, tools, diagnostic equipment, vehicle, etc.) in accordance with company policies. Maintains a high level of professional communication with team, customers, management, Sales and Technical Support. | 11/04/2024 |
| 2221 | Carlsbad Technology Carlsbad, CA Quality Assurance Assistant Bachelor’s degree Exp: Entry Level |
Perform and process in-process tests, perform other basic QA functions in raw materials, finished products and documentation when designated. | 11/04/2024 |
| 2222 | Catalent San Diego, CA Process Engineer I Master’s degree of Engineering Exp: 0+ years |
Catalent Pharma in San Diego, CA is hiring a Pharmaceutical Process Engineer I. The Pharmaceutical Process Engineer I reports to the Process Engineer Supervisor. An individual at the level of Process Engineer I will be expected to understand and execute basic setup, operation, troubleshooting, breakdown, and cleaning of designated small scale and pilot scale pharmaceutical manufacturing equipment under limited supervision. Equipment maintenance activities may include the purchasing and installation of spare parts and supplies. This individual will complete projects and demonstration batches, evaluating the formulation, equipment set points, and process procedures with supervision. Analysis of various product characteristics will be completed with minimal supervision. The Process Engineer I will participate in the technology transfer process to the manufacturing group and may participate in the batch record review process to identify risks. Other duties include supporting the manufacturing group in the GMP (Good Manufacturing Practices) suites as subject matter expert for designated projects. Other duties include the revision of SOPs (Standard Operating Procedures), as well as researching and onboarding new equipment under the direction of a senior engineer. | 11/04/2024 |
| 2223 | Catalent San Diego, CA Quality Control Chemist I Bachelor’s degree in Chemistry or Biochemistry highly preferred Exp: No exp |
Catalent Pharma in San Diego, CA is hiring a Quality Control (QC) Chemist I. The QC Chemist I will be responsible for performing various analytical techniques and common standard lab practices in order to assess the quality of pharmaceutical products under cGMPs (as applicable) and limited supervision. This position gives opportunities to broaden analytical understanding and learn the common operations in a fast-paced, early Phase-focused, dynamic Quality Control group. | 11/04/2024 |
| 2224 | Catalent San Diego, CA Process Engineer I Master’s degree of Engineering Exp: No exp |
Catalent Pharma in San Diego, CA is hiring a Pharmaceutical Process Engineer I. The Pharmaceutical Process Engineer I reports to the Process Engineer Supervisor. An individual at the level of Process Engineer I will be expected to understand and execute basic setup, operation, troubleshooting, breakdown, and cleaning of designated small scale and pilot scale pharmaceutical manufacturing equipment under limited supervision. Equipment maintenance activities may include the purchasing and installation of spare parts and supplies. This individual will complete projects and demonstration batches, evaluating the formulation, equipment set points, and process procedures with supervision. Analysis of various product characteristics will be completed with minimal supervision. The Process Engineer I will participate in the technology transfer process to the manufacturing group and may participate in the batch record review process to identify risks. Other duties include supporting the manufacturing group in the GMP (Good Manufacturing Practices) suites as subject matter expert for designated projects. Other duties include the revision of SOPs (Standard Operating Procedures), as well as researching and onboarding new equipment under the direction of a senior engineer. | 11/04/2024 |
| 2225 | Catalent San Diego, CA Associate Project Lead, Pre-Production Bachelor’s degree Exp: No exp |
Catalent Pharma Solutions is San Diego, CA is hiring an Associate Project Lead (PL) that will support pre-production teams in the management and successful delivery of assigned Projects for our Clinical Supply site. The Associate Project Lead serves as a liaison between cross functional teams to ensure project success while complying with regulatory requirements, good manufacturing practices (cGMP) and standard operating procedures (SOPs). The focus will be on understanding client needs and providing excellent customer service and proactive solutions. Under direction from PL team co-ordinate projects from award stage to completion. Primary responsibilities of this position include activities related to supply chain, procurement, batch record and label creation, and other project management and coordination activities affiliated with assigned projects. | 11/04/2024 |
| 2226 | Catalent Kansas City, MO Associate Scientist II, Biologics I Analytical Chemistry Bachelor’s Degree in Life Sciences or Physical Science field Exp: No exp |
Catalent Pharma Solutions in Kansas City, MO is hiring an Associate Scientist II, Biologics I who is primarily responsible for testing samples, drafting methods and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies. | 11/04/2024 |
| 2227 | Catalent Madison, WI Associate Engineer – Engineering Bachelor's degree in Engineering or related scientific field Exp: 1-2 years |
The Associate Equipment Engineering candidate will work on the Equipment team within the Engineering department. The candidate will interact with Operations, Supply Chain, Process Development, Validation, Procurement, Manufacturing Science and Technology (MS&T) and Quality. | 11/04/2024 |
| 2228 | Catalent Madison, WI Process Engineer - Manufacturing Science & Technology Master’s degree in a STEM discipline Exp: 0+ years |
The Manufacturing Sciences and Technology (MS&T) department’s primary function is to serve as an agile technical services team to support process & technology transfer (e.g., mAbs, fusion proteins, enzymes, mRNA, new modalities, etc.), process readiness and execution support related to documentation, equipment, consumables and materials, and technical writing. The MS&T organization supports the Madison facility as well as the Catalent Biologic’s network through client- facing support, on-the-floor or on-call technical coverage, as well as continuous improvement and site strategy projects. The Technology Transfer groups (Upstream and Downstream) are the technical liaisons between Process Development (internal or external) and at-scale GMP manufacturing relating to process transfer. This function includes drafting and supporting required batch documentation (i.e., gap assessments, reports, batch records, product impact), as well as process modeling and facility fit including initial bill-of-material development. | 11/04/2024 |
| 2229 | MilliporeSigma San Jose, CA Process Development Scientist Master’s degree in Chemical Engineering, Pharmaceutical Sciences, Life Sciences, Chemistry, or Biochemistry Exp: 1+ years |
MilliporeSigma is looking for a Process Development Scientist to join the technical branch of the commercial organization in the greater San Francisco Bay area. The Process Development Scientist is part of a worldwide team of engineers and scientists reporting into the technical support group for MilliporeSigma’s Process Solutions business. | 11/04/2024 |
| 2230 | MilliporeSigma Miamisburg, OH Associate Quality Scientist Bachelor’s Degree in Chemistry, Biology, or other Life Science Discipline Exp: 1+ years |
Evaluate stable isotope products, raw materials and in process materials according to established procedures. | 11/04/2024 |
| 2231 | MilliporeSigma Bedford, MA Scientist - Viral Vector Applications Bachelor’s degree in Chemical Engineering, Cell Biology, or other Science discipline Exp: 1+ years |
The Viral Vector Applications Scientist at MilliporeSigma in Bedford, MA will play a pivotal role in supporting development of cutting-edge tools and technologies for the rapidly evolving cell and gene therapy market. The successful candidate will join a dynamic Applications team within Process Solutions R&D, specializing in upstream viral vector processing. This group is responsible for generating application data to address customer needs, enhance knowledge in the field, and demonstrate the performance of products and processes for Adeno-Associated Virus (AAV) manufacturing. The scientist in this strategic lab-based position will independently manage experiments, execute studies, analyze data, and effectively communicate results. Collaboration is essential, as the role requires close interaction with a diverse range of technical and non-technical stakeholders encompassing both internal teams and external partners. | 11/04/2024 |
| 2232 | Cellares South SF, CA Cell Therapy Manufacturing Specialist Bachelor’s Degree Exp: 1+ years |
We are seeking an innovative and highly motivated Cell Therapy Manufacturing Associate to join our Process Sciences team who will contribute significantly to the development and manufacture of our advanced cell therapy manufacturing platform. The primary focus of this position will be to support manufacturing operations, as well as day-to-day lab operations. This is a hands-on position that will train in Process Development, Analytical Development, and/or MSAT prior to joining the Manufacturing Group. andidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows. | 11/04/2024 |
| 2233 | Cellipont Bioservices Woodlands, TX QA Technician II, Operations Bachelor's Degree Exp: 1-2 years |
Cellipont Bioservices is growing, and we are looking for a QA Technician II, Operations who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The QA Technician II, Operations will be responsible for monitoring systems and procedures to ensure compliance where applicable. The QA Technician II, Operations is responsible to provide Quality Assurance support real-time for GMP Manufacturing of master/working cell banks. This individual will be responsible for providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. | 11/04/2024 |
| 2234 | Cellipont Bioservices Woodlands, TX Quality Control Analyst I, Environmental Monitoring Bachelors Degree in Life Sciences Exp: 0-1 years |
Cellipont Bioservices is growing, and we are looking for a QC Analyst I, Environmental Monitoring (TEMP) who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The QC Analyst I, Environmental Monitoring (TEMP) is responsible for Environmental Monitoring sampling, analyzing, and reporting results, and microbiological testing to support manufacturing. Works in a fast-paced environment supporting the quality control department of a CMDO for manufacturing of cell therapy drug substance, sterile finished drug product, and fill/finish. The QC Analyst I, Environmental Monitoring (TEMP) is also responsible for ensuring all personnel activities are executed timely and cost effectively to ensure customer and stakeholder satisfaction. This role will also require the individual to demonstrate a strong ability to work cross-functionally. | 11/04/2024 |
| 2235 | Celularity Florham Park, NJ Operator, Tissue Manufacturing B.S degree in Biology, Bioengineering or related scientific discipline Exp: 1-2 years |
Celularity is seeking a dynamic individual to join a motivated team of clinical operators for the daily manufacture of multiple tissue product. Leveraging Celularity’s new, state-of-the-art cGMP capable facility, this position will make use of existing innovations and future technologies to meet and exceed manufacturing demand. | 11/04/2024 |
| 2236 | Celularity Morristown, NJ Associate Specialist, Quality Control Bachelor's degree in a scientific discipline Exp: 0-3 years |
The entry level Assoc. Specialist, QC - Temp to Perm role is responsible for supporting biobanking/ manufacturing requests. This includes the ability to interface with multiple groups, independently perform tasks, interpret results, and generate reports. | 11/04/2024 |
| 2237 | Centerline Biomedical Cleveland, OH Quality Engineer Bachelor's Degree in Engineering or related technical field Exp: 1-3+ years |
The Quality Engineer is an Exempt/Full-Time role responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 14971, ISO 13485:2016, MDSAP and FDA 21 CFR Part 820. This role supports supplier quality and monitoring primarily along with complaint/CAPA investigations, operations production and process controls, and product and service quality and the use of statistical techniques and other accepted quality principles. The Quality Engineer will also plan and execute activities concerned with the development, implementation, maintenance, and continuous improvement of Centerline’s quality systems. | 11/04/2024 |
| 2238 | Centrillion Palo Alto, CA Laboratory Technician B.A./B.S. Exp: 6 months |
We are looking for a Laboratory Technicians - multiple positions to join our R&D team in Palo Alto. The role is part of a small group that divides their focus between innovative new projects and product development. The ideal candidate will be extremely organized, familiar with basic laboratory techniques, and excited to learn and grow within the team. Technicians will divide their time between hands-on laboratory work, data analysis, and lab organization and maintenance. Candidates with knowledge and experience of PCR, library preparation, NGS sequencing or RNA seq will be given preference. | 11/04/2024 |
| 2239 | Cepheid Sunnyvale, CA Scientist II Master’s degree Exp: 0-2 years |
The Scientist II is a bench-level job focusing on real-time PCR and RT-PCR assay and product development in an FDA-QSR and ISO9001-compliant organization. The candidate will plan and execute laboratory research and demonstrate appropriate technical proficiency, scientific creativity, and collaboration with cross-functional departments. | 11/04/2024 |
| 2240 | Cepheid Sunnyvale, CA Scientist II Master’s degree in Molecular biology/Microbiology/Bioinformatics or related field Exp: 1+ years |
The Scientist II position is primarily a bench level R&D job focusing on real time PCR and RT-PCR assay and product development in an FDA-QSR and ISO9001 compliant organization. This position is part of Assay R&D and will be located in Sunnyvale, CA (Onsite). At Cepheid, our vision is to be the leading provider of seamlessly connected diagnostic solutions. | 11/04/2024 |
| 2241 | Cepheid Lodi, CA Manufacturing Engineer Master's degree Exp: 0+ years |
The Manufacturing Engineer II is responsible for sustaining and improving Medical Injection molding tools and processes to achieve plant manufacturing objectives for safety, quality, on-time performance, and customer satisfaction. This position will give me the opportunity to gain knowledge of using the Danaher Business Systems (DBS) tools in a manufacturing environment. This position is part of the Manufacturing Engineering Department and will be located in Lodi, CA. At Cepheid, our vision is to be the leading provider of seamlessly connected diagnostic solutions. | 11/04/2024 |
| 2242 | Cepheid Sunnyvale, CA Senior Scientist I Master’s degree in Molecular biology/Microbiology/Bioinformatics or related field Exp: 1+ years |
The Senior Scientist I position is a bench-level job focusing on real-time PCR and RT-PCR assay verification across GeneXpert platform instruments. The candidate will plan and execute analytical studies and demonstrate appropriate technical proficiency, scientific creativity, and collaboration with cross-functional departments. May lead small studies with manageable risks and resource requirements as well as lead others to resolve project related issues. This position is part of Assay R&D and will be located in Sunnyvale, CA (Onsite). At Cepheid, our vision is to be the leading provider of seamlessly connected diagnostic solutions. | 11/04/2024 |
| 2243 | Cepheid Lodi, CA Process Engineer - Day Shift Bachelor’s degree Exp: 0-1+ years |
The Process Engineer supports manufacturing operations with scientific expertise to ensure successful transfer of new products from development to manufacturing ensuring robust manufacturing processes at commercialization; failure investigation of commercialized products; support processes to ensure performance within expected parameters. Includes laboratory roles. Schedule for this role would 5am-1pm, Thursday-Monday, with Tuesday and Wednesday off. | 11/04/2024 |
| 2244 | Cepheid Lodi, CA Process Engineer- Split Shift Bachelor’s degree Exp: 0-1+ years |
The Process Engineer supports manufacturing operations with scientific expertise to ensure successful transfer of new products from development to manufacturing ensuring robust manufacturing processes at commercialization; failure investigation of commercialized products; support processes to ensure performance within expected parameters. Includes laboratory roles. Schedule for this role will be 1pm-9pm, Monday- Friday with Saturday and Sunday. | 11/04/2024 |
| 2245 | Cepheid Lodi, CA Process Engineer- Night Shift Bachelor’s degree Exp: 0-1+ years |
The Process Engineer supports manufacturing operations with scientific expertise to ensure successful transfer of new products from development to manufacturing ensuring robust manufacturing processes at commercialization; failure investigation of commercialized products; support processes to ensure performance within expected parameters. Includes laboratory roles. Schedule for this role will be 9pm-5am Thursday-Monday with Tuesday and Wednesday off. | 11/04/2024 |
| 2246 | Charles River Memphis, TN Biomanufacturing Technician I BS in a scientific field Exp: 0-1 years |
The BioManufacturing Technician I is responsible for performing various manufacturing activities related to the start-up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to work night, weekends, and holidays. Must be able to meet physical requirements established in this job description. | 11/04/2024 |
| 2247 | Charles River Wayne, PA Scientist 1 Biophysical 1 Bachelor’s degree (B.S.) or equivalent in biochemistry, chemistry or related discipline. Exp: 1-3 years |
Serve as the Scientist responsible for the development and execution of moderately complex testing and characterization of biotherapeutics using biophysical instrumentation and methodologies. May be independently responsible for method feasibility, method development, method optimization, method transfers, method qualifications, method validations and routine testing under both R&D and cGMP environments. Additionally, will be responsible for management of projects including client interaction, interpretation and reporting of data of assigned research projects. | 11/04/2024 |
| 2248 | BioMérieux Durham, NC Quality Floor Support - 2nd Shift Bachelor’s Degree in Engineering, Biotechnology, Microbiology, or Biology Exp: 0 years |
The Quality Floor Support (QFS) Specialist 1 is responsible for providing quality oversight and guidance on the production floor. In this capacity, they identify and resolve exceptions in production areas and review data and records for GMP compliance. The QFS Specialist 1 routinely performs and documents walkthrough audits of bioMérieux production, warehouse and support areas. They support quality continuous improvement and investigation activities, including but not limited to customer complaints, nonconformance investigations and CAPAs. | 10/28/2024 |
| 2249 | BioMérieux Philadelphia, PA QC Engineering Technician Bachelors degree in Biology or related field Exp: 0-2 years |
Conducts activities within the Quality Control functions testing and release of finished product and any applicable in-Process audits (ensuring that manufacturing operations remain in control). This job serves as the lab technician in the QC group and entails ensuring availability of materials for QC testing, organization of lab processes and ensuring equipment is maintained / calibrated as appropriate, and departmental documentation is current and accurate. Responsible for ensuring deviations are properly documented, nonconforming material is segregated and secured, and the supporting of any projects assigned. Performs all duties using safety conscious practices. Individual must inspect/test/audit materials & processes in a timely fashion while, at the same time, ensuring conformance to all requirements | 10/28/2024 |
| 2250 | BioMérieux Salt Lake City, UT Research Associate I Bachelor’s degree in a scientific discipline Exp: 6 months |
The Research Associate I (RA I) works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g., nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to communicate and coordinate with peers and supervisor(s) effectively and respectfully. The position requires basic laboratory technical skills, organizational skills, attention to detail, critical thinking, troubleshooting and problem-solving, and a dedication to the mission and goals of the department and bioMérieux. A Research Associate I may receive general or detailed instruction and direct supervision on general work, new procedures, and assignments. | 10/28/2024 |
| 2251 | BioMérieux Hazelwood, MO Scientist - Tech Transfer M.S. in medical technology, biochemistry, or microbiology Exp: 1+ year |
The Industrialization department at bioMerieux is seeking a Scientist to lead transfer of drug development into manufacturing. The scientist performs process validations and provides development support which includes data review, perform experiments, and risk assessments. This individual job function would be to provide technical knowledge of manufacturing needs and support project team. | 10/28/2024 |
| 2252 | Biogen Research Triangle Park, NC Manufacturing Associate Bachelor’s Degree (STEM preferred) Exp: Recent Grad/Entry Level |
Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; with two main areas/disciplines – Upstream (Cell Culture) and Downstream (Purification). MAs perform these critical steps within Current Good Manufacturing Practice (cGMP) biosafety cabinets and cleanroom suites. | 10/28/2024 |
| 2253 | Biogen Research Triangle Park, NC Manufacturing Associate IV Bachelor’s Degree (STEM preferred) Exp: 6 months |
Manufacturing Associates perform processing steps and manufacturing support activities in our facilities in Research Triangle Park (RTP). These teams are the backbone of our operations – each person playing a critical role in delivering our therapies to the patients who need them. This position will be in our Parenteral Filling operations, and our teams operate across the following units: Component Preparation, Compounding, Parenteral Filling/Lyophilization, Visual Inspection | 10/28/2024 |
| 2254 | Biogen Research Triangle Park, NC Engineer III, Manufacturing Sciences Anti-Sense Oligonucleotide M.S. in Biochemistry, Bioengineering, Biochemical, Chemical Engineering or related discipline Exp: 0-2 years |
The Engineer III, Manufacturing Sciences, will provide technical expertise to the clinical, PPQ, and commercial manufacturing campaigns run within the OSM facility. | 10/28/2024 |
| 2255 | BioLegend San Diego, CA Research Associate I - Antibody Applications Bachelor’s Degree in Biology, Immunology, Biochemistry, Neuroscience or other related fields Exp: 1 year |
Biolegend’s Research Associate position conducts antibody characterization and supports product development in Immunology, Oncology, Stem Cells and Neuroscience, encompassing various antibody applications including SDS-Page and Western blot, Immunoprecipitation, ELISA, flow cytometry, immunocytochemistry, immunohistochemistry, etc. This position will be responsible for effectively collecting, communicating and summarizing experimental data. | 10/28/2024 |
| 2256 | BioLegend San Diego, CA Biochemist I - ELISA BS/BA in Biology, Chemistry, or other life science related field Exp: 1+ years |
BioLegend is seeking a highly motivated Manufacturing Associate to join the Biomarker Immunoassay team in San Diego. The Manufacturing Associate will be working closely with others in the team to ensure timely manufacturing of high-quality immunoassay products under ISO13485 standards. This role will be responsible for all aspects of product manufacturing including planning/scheduling, making and testing immunoassay components and kits, troubleshooting issues associated with product quality, and documenting and reviewing production batch records to ensure accuracy and completeness. Additional responsibilities include working with the Product Development team to ensure proper transfer of new products from Product Development to Manufacturing, filling daily immunoassay kit orders from inventoried components, and making and testing custom products in a timely manner. | 10/28/2024 |
| 2257 | BioLife Solutions Bothell, WA Aseptic Technician II Bachelor’s degree Exp: 1 year |
The Aseptic Technician is a core team member of the manufacturing team. The Aseptic Technician is responsible for daily production including environmental monitoring, formulating, and filling of aseptic GMP manufactured products according to batch records and SOPs. This position is for an experienced manufacturing professional with knowledge of GMP, aseptic technique, and problem-solving skills. This position provides an opportunity to solve challenges in a fast-growing industry. BioLife is a fast-growing company that is the leading cell preservation specialist within the fields of biotechnology and pharmaceuticals. This position allows for exposure to many department’s ways of working and opportunities for cross functional projects. Allows for insight into the world of biotechnology. | 10/28/2024 |
| 2258 | Biolog Newark, DE QC Scientist Master’s degree in Life Science Exp: 1+ year |
Biolog Lab Services is seeking a detail-oriented and collaborative QC Scientist to join our growing team. In this role, you will be responsible for performing data analysis and quality control checks on all outgoing Certificates of Analysis (CofAs) and reports. We’re looking for someone who is passionate about ensuring the highest standards of accuracy, while also being a team player who is willing to support colleagues and contribute to our dynamic work environment. | 10/28/2024 |
| 2259 | Biomeme Philadelphia, PA Scientist - Biology R&D MS in Biology, Biochemistry, Biotechnology, or related laboratory science Exp: 0-2 years |
Scientists at Biomeme serve cross-functional roles, with the majority of time at the bench in support of R&D of Biomeme’s novel nucleic acid detection and extraction technologies. Scientists may be asked to work semi-independently on projects and may also interface with other groups such as Quality and Engineering in support of their efforts. | 10/28/2024 |
| 2260 | Biomere Richmond, CA In Vivo Research Associate I BS Degree in Science Exp: 1-2 years |
Research Associate works under the direct guidance of the Project Manager- Research and the general guidance of the senior staff. Research Associate is proficient in animal procedures/animal husbandry, grant, internal, and/or contract research studies according to the study protocols and to the company guidelines and standard operating procedures (SOPs). | 10/28/2024 |
| 2261 | Bionova Fremont, CA Downstream Manufacturing Associate BS in Life Sciences, or related discipline Exp: 0-1 years |
The Downstream Manufacturing Associate or Technician will actively contribute to the manufacturing and technology transfer projects at the Bionova Scientific Fremont location. As part of the Purification/Manufacturing group, you will have opportunities to work on a wide-ranging set of projects for troubleshooting and investigations, system and workflow implementation, and tech transfers of processes into the GMP manufacturing facility. The role will provide hands-on execution of complex experiments in a team setting. The role will support GMP readiness and manufacturing activities. The scope of responsibilities may include but are not limited to Document writing (SOPs, Equipment URSs, etc.), equipment validation execution support and single-use assembly design. | 10/28/2024 |
| 2262 | Bio-Rad Pleasanton, CA Research Associate II Bachelor's or Master’s degree in Molecular Biology, Biochemistry, Genetics, or related life science field Exp: 1-5 years |
Join Bio-Rad’s Life Science Group in developing innovative products for oncology research and biopharmaceutical testing applications. As part of an interdisciplinary team, you will contribute to the development of new products utilizing state-of-the-art droplet digital PCR (ddPCR) technology. Your responsibilities will include planning and conducting experiments, designing and optimizing ddPCR assays, analyzing and presenting data, and problem-solving. You will be involved in all stages of the product development process from proof-of-concept through launch and will help deliver applications and products that empower our customers to improve healthcare outcomes for millions. | 10/28/2024 |
| 2263 | Bio-Rad Hercules, CA Quality Engineer I Bachelor’s degree or equivalent in a related scientific discipline Exp: 0-2+ years |
The candidate will attend cross function Daily Management meetings and represent QA following up on blocking issues and implementing countermeasures. The candidate will manage the Material Review Board and ensure thorough documentation of non-conformities and risk based determination of CAPA. The candidate will review data for trends, manage corrections and corrective action and support GSC and business partners as requested. | 10/28/2024 |
| 2264 | Bio-Rad Woodinville, WA Quality Engineer I Bachelor’s degree or equivalent in a related scientific discipline Exp: 0-2+ years |
Join Bio-Rad as our Quality Engineer and work in our Woodinville, WA site! Working in this Quality Assurance role, you will attend cross functional Daily Management meetings and represent Quality Assurance to address blocking issues and implement counter measures. You will manage the Material Review Board and ensure thorough data-driven documentation of non-conformities and risk based determination of CAPA. You will review data for trends, manage corrections and corrective action and support Global Supply Chain and business partners as requested. | 10/28/2024 |
| 2265 | Bio-Rad Hercules, CA QC Specialist I - Temporary Bachelor's degree or equivalent in a life science (Chemistry, Biology) or related field Exp: 0-2 years |
A typical day will involve completion of testing on assigned batches and completing paperwork/data entry into SAP to document results for review/product release. This role requires communication and coordination between team members, the supervisor and the planners to ensure that we are keeping on top of priorities to avoid backorder. Besides routine testing, a day will include attending the daily Tier 1 meetings to report on safety, quality, delivery and inventory updates. | 10/28/2024 |
| 2266 | BioRestorative Therapies Melville, NY cGMP Bio -Manufacturing Engineer MSc degree in cell biology or similar discipline Exp: 1-6 years |
BioRestorative Therapies, Melville, NY is recruiting for a cGMP bio-manufacturing engineer. This role provides outstanding opportunities for talented self-motivated individuals, ideally with experience in (stem) cell biology, immunology, and/or molecular biology, who can contribute to our ongoing efforts to generate clinical grade cell-based therapeutics. We are most interested in connecting with qualified individuals who aspire to support the development of therapeutics and/or life science products and tools to support research endeavors. | 10/28/2024 |
| 2267 | Bio-Techne Minneapolis, MN Advanced Research Associate Master's degree in chemistry, biological sciences, or equivalent (chemistry or biochemistry preferred) Exp: 0-2 years |
As an Advanced Research Associate in the Conjugation lab, you will be responsible for preparing conjugated proteins, antibodies, enzymes, oligonucleotides, and microparticles for both manufacturing and research purposes. In addition, you may help prepare and test other chemistry related reagents for manufacturing and QC teams. This is a fantastic opportunity for you to grow your analysis, problem solving, and troubleshooting experience in a collaborative and energetic biotech manufacturing environment. You will find that this position offers continuous learning and development as you grow your product knowledge, technical manufacturing & testing expertise, and engage in a variety of lab techniques every day. | 10/28/2024 |
| 2268 | Bio-Techne Minneapolis, MN Quality Technician Bachelor’s degree in Biology, or related field of study Exp: 0-1 year |
This position will require setup, maintenance, troubleshooting, and operation of QC hematology analyzers. This position will require monitoring instrument performance throughout the QC process and troubleshooting the instrument when necessary. This position will test hematology products for homogeneity during the bottling process by following established methods. The expectation for this position is to setup and QC product on 50% of the laboratory instruments and troubleshoot as necessary. Other tasks include proofing labels and assay sheets. This position will adhere to safety regulations. Perform additional duties as assigned. | 10/28/2024 |
| 2269 | Bio-Techne San Marcos, CA QC Specialist Bachelor’s degree in Biological Science, Chemistry, or related field Exp: 1-5 years |
Responsible for performing QC testing for Value Assignment assays, QC release assays, stability, physical/visual inspections, any related QC function. Assists in the flow of product in the QC department. | 10/28/2024 |
| 2270 | Bio-Techne Minneapolis, MN Research Associate Bachelor’s degree in biochemistry, microbiology, biotechnology,?or equivalent Exp: 0-2 years |
This position is responsible for the growth of E. coli in a GMP (Good Manufacturing Practice) Lab, following GMP guidelines. This includes, but is not limited to GMP, AF (Animal Free Process), and other products used by pharma and IVD customers. This position manufactures E. coli clones using shake flask, or Bioreactors using a variety of techniques, software and equipment including, Bioreactors, Shake Flasks, Biosafety cabinets, Fume Hoods, Sterile Filters, Autoclaves, and centrifuges. All procedures and batch records follow GMP guidelines. | 10/28/2024 |
| 2271 | Bio-Techne Minneapolis, MN Advanced Research Associate Master's degree in a biological science Exp: 0-2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins and monoclonal antibodies for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for production, media and supplement preparation, and additional duties as assigned. This position requires weekend work with a Tuesday - Saturday shift. | 10/28/2024 |
| 2272 | Bio-Techne Minneapolis, MN Research Associate, Mammalian Cell Culture Bachelor’s degree in a biological science Exp: 0-2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins and monoclonal antibodies for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for production, media and supplement preparation, and additional duties as assigned. This position requires weekend work with a Tuesday - Saturday shift. | 10/28/2024 |
| 2273 | Bio-Techne Wallingford, CT Quality Technician Bachelor of Science degree in relevant field Exp: 0-2 years |
The Quality Technician role is established to support the Simple Plex Consumables team in the Wallingford facility. Assists Quality Analysts and the QA team in our ISO compliant environment. Provides support for QC / QA activities including: hands-on evaluation of microfluidic cartridge products. | 10/28/2024 |
| 2274 | Bora Pharmaceuticals Camden, MD Analyst l, QC Microbiology-3rd-Shift BS in Microbiology/Biology or related field. Exp: 0-2 years |
Responsible for conducting qualitative and quantitative microbial analyses in support of environmental monitoring, cGMP manufacturing and stability of drug products and incoming raw materials. This position supports our 3rd-shift, working 10pm-6:30am, Monday through Friday. | 10/28/2024 |
| 2275 | Bora Pharmaceuticals Camden, MD Analyst II, QC Microbiology-2nd Shift MS in Microbiology/Biology or related field Exp: 0-2 years |
The Analyst II, QC Microbiology position supports the Quality Control group at Bora Pharmaceuticals Camden site to maintain process optimization and manufacturing activities. The Microbiologist is responsible for performing activities in support of the Microbiology, Environmental Monitoring, and Utility testing programs, which includes microbiological product testing, monitoring of the manufacturing production space, and supporting quality initiatives. The individual routinely conducts monitoring, testing, and SOP generation and revision. This position is a for our 2nd shift, working hours; 2pm-10:30pm Monday through Friday. | 10/28/2024 |
| 2276 | Bora Pharmaceuticals Camden, MD Analyst l, QC Microbiology-3rd-Shift BS in Microbiology/Biology or related field. Exp: 0-2 years |
Responsible for conducting qualitative and quantitative microbial analyses in support of environmental monitoring, cGMP manufacturing and stability of drug products and incoming raw materials. This position supports our 3rd-shift, working 10pm-6:30am, Monday through Friday. | 10/28/2024 |
| 2277 | Bora Pharmaceuticals Camden, MD Analyst I, QC Analytical B.S. in Chemistry or related field Exp: 0-2 years |
Perform analytical testing per cGMP in support of raw material, in-process, final product, stability. Typical hours are 10:00 pm – 6:30 am, Monday through Friday. Hours may vary to meet business and training needs. | 10/28/2024 |
| 2278 | Bora Pharmaceuticals Camden, MD Analyst III, Quality Assurance-Batch Release BS or MS degree in Chemistry/Biology or related discipline Exp: BS: 1-3 years; MS: 1 year |
The QA Analyst III is responsible for performing duties related to the management of records relevant to the review and release of Batch Records for the cGMP operation at Bora Pharmaceutical, the Baltimore Camden Site. Our QA Department provides expertise in problem solving and process improvements. The QA Analyst will interact with all departments to provide guidance necessary to maintain and improve cGMP compliance at the company. | 10/28/2024 |
| 2279 | BIB Southborough, MA Research Associate - Downstream Process Development BS degrees in biology, biochemistry, biomedical/biochemical engineering, or related fields Exp: 0-1 year |
A Research Associate I is an entry level position for Bachelor’s degree with no prior experience and reports to a scientist level or above on relevant projects. The individual is responsible for routinely setting up, operating, and maintaining the downstream lab equipment under direct supervision at BIB. | 10/28/2024 |
| 2280 | BostonGenes Waltham, MA Biospecimen Inventory Technician BS in a Biological or Life Science Exp: 1 year |
The candidate will report to the Lab Manager and under their supervision support BostonGenes laboratory teams with sample management and tracking systems/protocols. The candidate will create and oversee a new sample inventory tracking system using the existing Lab Information Management System (LIMS) and Benchling software. Once created they will assist in the transition to an end-to-end barcoding-based system for sample tracking and continuously update and improve the process as new tests are added. This candidate will also be responsible for handling and processing blood specimens for specific projects. This will involve basic blood processing techniques such as blood fractionation, plasma clarification, and cell isolation for downstream biobanking. | 10/28/2024 |
| 2281 | BroadPharm San Diego, CA QC Chemist Bachelor or MS degree in Analytical Chemistry or Organic Chemistry Exp: 1-4 years |
BroadPharm is a fast-growing biotech company which specializes in providing high purity PEG products and customer services worldwide. We are seeking a highly motivated QC Chemist to join our expanding team. The ideal candidate would already have 1+ year of working experience with HPLC, MS, and NMR. The position will work closely with the production team and regulatory manager in addition to the current QC staff. | 10/28/2024 |
| 2282 | BWX Technologies Erwin, TN Engineer 1 Bachelor’s degree in Engineering, Biotechnology, Microbiology, or Biology Exp: No exp |
Responsible for routine engineering assignments applying standard engineering techniques, procedures, and criteria under guidance of a manager or experienced engineer. Assignments are designed to develop professional work knowledge and abilities. Works under close supervision. Manager screens assignments for unusual or difficult problems and selects techniques and procedures to be applied on non-routine work. | 10/28/2024 |
| 2283 | BWX Technologies Mt Vernon, IN Manufacturing Engineer Bachelor's degree in Mechanical, Manufacturing, or Civil Engineering Exp: Entry Level |
BWXT is currently seeking a Manufacturing Engineer to join our growing team in Mt. Vernon, IN! Position responsibilities include: Serve as the primary point of contact/coordinator for the program.Assist in developing detailed recovery plans for projects. Perform reviews of contract and design requirements for acceptance of quality notifications. Track status of project schedules and deliverables. Work with Unit Manager to maintain contract performance metrics. Interface with Design and Manufacturing. Engineering to manage change to component designs. Support quotes for new work by reviewing technical requirements and preparing person-hour estimates. Perform special assignments as deemed necessary. | 10/28/2024 |
| 2284 | BWX Technologies Erwin, TN Engineer 2 -- AUKUS Design Engineering -- Process MS Degree -- Engineering Exp: 1 year |
Evaluates situations, selects and applies standard engineering techniques, procedures and criteria, using judgment in making minor modifications. Assignments have a clear objective and require planning and investigation of limited number of possibilities. Work is reviewed for application of sound judgement and compliance with contract technical requirements and meeting of Division policies and procedures. Receives instructions on specific assignment objectives, complex features and possible solutions. Assistance is furnished on unusual problems and work is reviewed for application of sound professional judgment. | 10/28/2024 |
| 2285 | BWX Technologies Erwin, TN Engineer 2 -- AUKUS Elec & Instrumentation Eng MS Degree -- Engineering Exp: 1 year |
Evaluates situations, selects and applies standard engineering techniques, procedures and criteria, using judgment in making minor modifications. Assignments have a clear objective and require planning and investigation of limited number of possibilities. Work is reviewed for application of sound judgement and compliance with contract technical requirements and meeting of Division policies and procedures. Receives instructions on specific assignment objectives, complex features and possible solutions. Assistance is furnished on unusual problems and work is reviewed for application of sound professional judgment. | 10/28/2024 |
| 2286 | BWX Technologies Erwin, TN Engineer 2 -- AUKUS Design Engineering -- Mechanical MS Degree -- Engineering Exp: 1 year |
Evaluates situations, selects and applies standard engineering techniques, procedures and criteria, using judgment in making minor modifications. Assignments have a clear objective and require planning and investigation of limited number of possibilities. Work is reviewed for application of sound judgement and compliance with contract technical requirements and meeting of Division policies and procedures. Receives instructions on specific assignment objectives, complex features and possible solutions. Assistance is furnished on unusual problems and work is reviewed for application of sound professional judgment. | 10/28/2024 |
| 2287 | BWX Technologies Erwin, TN Nuclear Safety Eng 1 MS Degree -- Engineering Exp: 1-2 years |
Performs Nuclear Criticality Safety (NCS) activities that assure plant operations are conducted in compliance with governmental regulations and license conditions and in a manner such that a criticality excursion and its consequences will not occur. | 10/28/2024 |
| 2288 | ATEC Carlsbad, CA Systems Engineer I BS Degree in Engineering Exp: 0-2 years |
The Systems Engineer will be a key participant in many steps along the product development pathway, including system requirements development and documentation, development testing, design verification testing, Design History File compilation, validation and iterative improvement processes. | 10/22/2024 |
| 2289 | AustinPx Georgetown, TX Process Engineer I Bachelor’s Degree in Engineering, Chemical Engineering Exp: 0-2 years |
Work within a cGMP quality system, including participating in manufacturing activities under limited supervision. Complete process development and scale up activities in collaboration with formulation development and manufacturing to enable clinical trial material manufacturing. Prepare master batch records (MBRs). Utilize statistical design of experiment and process control schemes to optimize outcomes. Solve technical issues relating to the manufacture of dose form/product using process analysis tools. Design Experiments to investigate the relationships between material attributes, process parameter/equipment selection, and product quality. Generate process development/optimization protocols and reports. Assist with all necessary activities to procure and install equipment, including developing requirements, setting up, qualification protocol writing & execution, SOP development. Scale up of manufacturing processes from pilot to commercial scale. Participate in process technical transfer of manufacturing processing to 3rd party Contract Development and Manufacturing Organizations (CDMOs) to enable commercial manufacturing. Travel to CDMOs to oversee process transfer and manufacturing. Develop a strong understanding of specific equipment utilized internally and at CDMOs. | 10/22/2024 |
| 2290 | Avance Biosciences Houston, TX Lab Associate II BS in Biochemistry, Molecular Biology, or related field Exp: 1+ years |
Perform analytical experiments following company SOPs and instructions from superiors. Maintain good documentation and assist in problem solving. Strictly following FDA regulations (GLP and CGMP) while executing experiments | 10/22/2024 |
| 2291 | Avantor Sciences Irving, TX Project Engineer 1 Bachelor’s degree in Mechanical, Electrical, or Chemical Engineering Exp: 1-3 years |
Works independently under close supervision, responsible for the engineering and technical disciplines needed to complete a project. Plan projects, establish project criteria, coordinate project reviews, and ensure the proper implementation of project elements. Formulate project parameters and assigning responsibilities to the most capable employees and monitoring the project team. Create frameworks to measure the project's metrics and data collection. | 10/22/2024 |
| 2292 | Avantor Sciences Bridgewater, NJ Associate Scientist - Upstream (mRNA) BS (biochemistry, molecular biology, cell biology, chemical engineering, bioengineering or related). Exp: 1+ year |
The successful Associate Scientist - Upstream (mRNA) candidate will bring an eagerness to learn, strive for highly productivity, be well-organized and self-motivated. This high potential role will be responsible for the hands-on execution of cell culture laboratory experiments for the process development and basic analytical studies. The hired candidate will make detailed observations, analyze data, interpret results, and exercise appropriate technical judgment in the execution of studies. | 10/22/2024 |
| 2293 | Avid Bioservices Tustin, CA Manufacturing Associate, Downstream Bachelor’s with a preference for Biology or Chemistry emphasis. Exp: 1-2+ years |
Join our dynamic team as a Manufacturing Associate, Downstream! In this role, you'll be a crucial part of our multi-product manufacturing facility, working in strict compliance with cGMP and Standard Operating Procedures. Your responsibilities will encompass various tasks, including production, meticulous documentation, report writing, materials procurement, and equipment scheduling. You'll be instrumental in ensuring the timely production and release of top-quality products. At our company, we value core principles such as Integrity, Adaptability, Innovation, Teamwork, and Passion, all united by a shared mission to enhance patients' lives through the consistent delivery of high-quality biopharmaceuticals. If you're ready to make a meaningful impact, apply now and be part of our journey! | 10/22/2024 |
| 2294 | AXIS Dilworth, MN Analytical Chemist I Bachelor’s degree in Biology, Chemistry, or equivalent. Exp: 1 year |
The Analytical Chemist I, Bioanalytical Operations carries out various Bioanalytical functions of the organization. The Analytical Chemist is responsible for executing Bioanalytical methods within AXIS Clinicals. | 10/22/2024 |
| 2295 | AxisPharm San Diego, CA Lab Technician Bachelor’s degree Exp: 0-4 years |
Maintain inventory accuracy and erform database reconciliation on daily basis. Familiarity with automated laboratory equipment, scientific database, E-notebook a plus. Assist with laboratory support tasks such as documentation management, shipping/receiving. Adheres to laboratory safety standard, including proper use of PPE, safety enclosures and other equipment. | 10/22/2024 |
| 2296 | BA Sciences Morrisville, NC QA Specialist I Bachelor’s degree in a related science discipline Exp: 0-3 years |
The Quality Assurance Specialist supports the QA Lead and the company’s quality program by auditing analytical data, routine work, protocols and reports. | 10/22/2024 |
| 2297 | BA Sciences Salem, NH Analytical Chemist I, RM Bachelor’s degree in Chemistry or a related discipline Exp: 0-3 years |
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties include performing analysis of Raw Materials using AA, UV-Vis, and Wet Chemical Analysis according to USP/EP methods. | 10/22/2024 |
| 2298 | BA Sciences Salem, NH Microbiologist I - Microbiome BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The Microbiologist I conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 10/22/2024 |
| 2299 | BA Sciences Salem, NH Microbiologist I, QC BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The QC Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 10/22/2024 |
| 2300 | BA Sciences Salem, NH Microbiologist II, Microbiome BA or BS degree in Microbiology or related science discipline Exp: 1-5 years |
The Microbiologist II conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 10/22/2024 |
| 2301 | Bachem Vista, CA Chemist Bachelor’s degree in chemistry or related scientific field Exp: 0-2 years |
The Chemist function is to work in a cGMP regulated environment manufacturing active pharmaceutical products (APIs) as well as performing related activities at Bachem. | 10/22/2024 |
| 2302 | Baxter Saint Paul, MN Sterility Associate I BS Degree in Science, Engineering or Math or other relevant field Exp: 1+ year |
As the site Sterility Associate, you will serve as the primary resource for the team and support development, validation and maintenance of sterilization processes and cleanroom certification. This position plays a substantial role in the qualification and/or validation of sterilization, cleanroom, equipment, raw materials, and manufacturing processes. In this role you will directly impact the health and safety of our end-users, our patients. | 10/22/2024 |
| 2303 | Baxter Hayward, CA Analyst I, Quality Control Lab Bachelor’s degree in Chemistry or Biological Sciences with Analytical Chemistry Exp: 0-2 years |
Conduct specific chemical and physical analysis on medical devices through all stages of the manufacturing process from incoming raw materials to finished goods. Responsible for overall sample and materials management activities supporting the QC laboratory. | 10/22/2024 |
| 2304 | Baxter Medina, NY Manufacturing Engineer Bachelor’s degree in engineering (Biomedical, Mechanical, Industrial, Electrical or Chemical Engineering) Exp: 1-3 years |
This description outlines the employment prerequisites and job responsibilities for the position of Manufacturing Engineer within the Continuous Improvement Team. Provide support in the execution of the site’s operational optimization and quality improvement projects to achieve Medina Plant goals and objectives. Drive/support various quality improvement, business continuity/expansion, and cost reduction initiatives from identification through implementation while working with cross functional resources to ensure results are achieved in a timely manner. | 10/22/2024 |
| 2305 | Baxter Round Lake, IL Quality Lab Associate I Bachelors degree in Chemistry or Science related degree Exp: 6+ months |
The Position encompasses the biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs. **This is a first shift position that will be required to work on Saturday to Tuesday to support training of analysts and to support projects and/or production, as required.** A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials. | 10/22/2024 |
| 2306 | Baxter Cleveland, MS Process Engineer - Injection Molding Bachelor's Degree in Engineering Required (Mechanical, Industrial, Electrical, Chemical, or Polymer Science degrees are preferred) Exp: 0-2 years |
This position is a key role in the Injection Molding Operations. Primary focus will be on implementing continuous improvement, new business, and capacity expansion projects. Additional focus will also be on manufacturing equipment reliability and process support work within the Injection Molding Operations. You will also be involved in Multi-functional project management within this role. | 10/22/2024 |
| 2307 | Baxter Cleveland, MS Process Engineer - Bottled Solutions Bachelor's degree in engineering required. (Mechanical, Industrial, Electrical, or Computer degrees are preferred) Exp: 0-2 years |
This position is a key role in the Bottled Solutions Operations. Primary focus will be on implementing continuous improvement, new business, and capacity expansion projects. Additional focus will also be on manufacturing equipment reliability and process support work within the Bottled Solutions Operations. Multi-functional project management will be involved in this role as well. | 10/22/2024 |
| 2308 | Baxter Mountain Home, AR Quality Lab Associate Bachelor of Science in Chemistry Exp: 0-2 years |
Responsible for the outgoing quality, safety, and efficacy of product produced at Mountain Home (relative to Chemistry Laboratory analyses) involving complex routine and non-routine testing and validation in the Chem Lab. | 10/22/2024 |
| 2309 | Inotiv Rockville, MD Quality Assurance Auditor I B.S. in chemistry or life sciences or B.S./B.A. in related field Exp: 1-3 years |
Interact with clients, other employees, and the community in a professional manner. Support and participate in company initiatives as directed. Maintain thorough knowledge of facility SOPs, policies, study protocols, etc. Adhere to all safety regulations and procedures. Provide assistance or support to other Inotiv QA team members as necessary. Perform other duties as assigned. | 10/22/2024 |
| 2310 | Inotiv Raleigh, NC Associate Scientist Bachelors Degree biology or related field Exp: 0-1+ years |
Conduct GLP and non-GLP genetic toxicology assays (i.e. Ames, Comet, and micronucleus assays). Maintain and dose cultured cells, including primary cells and stem cells. Perform laboratory maintenance tasks (e.g. material storage and disposal, equipment monitoring/maintenance, etc.). Assist in the maintenance of supply inventories. Maintain study books. Handle data (e.g. organize data, prepare data tables). Train others in basic lab skills. Perform peer reviews of laboratory records and study documentation. Participate in the Quality Assurance audit process. | 10/22/2024 |
| 2311 | Inotiv Raleigh, NC Associate Scientist Bachelors Degree biology or related field Exp: 0-1+ years |
Conduct GLP and non-GLP genetic toxicology assays (i.e. Ames, Comet, and micronucleus assays). Maintain and dose cultured cells, including primary cells and stem cells. Perform laboratory maintenance tasks (e.g. material storage and disposal, equipment monitoring/maintenance, etc.). Assist in the maintenance of supply inventories. Maintain study books. Handle data (e.g. organize data, prepare data tables). Train others in basic lab skills. Perform peer reviews of laboratory records and study documentation. Participate in the Quality Assurance audit process. | 10/22/2024 |
| 2312 | Bausch + Lomb Rochester, NY Scientist I, R&D Microbiology B.S. or M.S. Exp: 0-3 years |
Monitoring product quality by performing tests to support marketed and pre-marketed product formulations in accordance with SOPs and regulations. | 10/22/2024 |
| 2313 | Beckman Coulter Diagnostics Chaska, MN Manufacturing Controls Engineer II Master's degree in engineering Exp: 0+ years |
The Manufacturing Engineer II for Beckman Coulter Diagnostics is responsible for supporting our reagent operations equipment, assessing equipment for optimization, qualifying replacements, monitoring our processes and driving to exceed our customer’s demands to ensure our patients have the tests they need. This position is part of the Reagent Operations located in Chaska and is on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Manufacturing Engineering team and report to the Process Engineering Manager responsible for the design, implementation and support of manufacturing processes, and equipment. If you thrive in a fast-paced role and want to work to build a world-class manufacturing organization. | 10/22/2024 |
| 2314 | Beckman Coulter Diagnostics Miami, FL System Integration Engineer Master’s degree in a related Engineering discipline (Electrical Engineering, Mechanical, Biomedical, Systems Engineering) Exp: 0+ years |
The Systems Integration Engineer for Beckman Coulter Diagnostics will be a critical team member working cross-functionally on programs developing new products, and in supporting legacy instrumentation in cost reduction, product design changes due to regulatory and environmental standard revisions, and customer driven product enhancements. This position is located in Miami, FL with the Hematology/Urinalysis Business Unit, and is on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will work within the Systems Engineering team and report to the Senior Manager of Systems and Hardware, New Product Development responsible for leading design tasks that create novel hardware, fluidics and electronics, and for integrating these systems, along with reagents and algorithms, into world-class clinical diagnostics analyzers. If you thrive in an amazing, innovation-oriented, challenging role and want to work to build an amazing systems engineering and test organization. | 10/22/2024 |
| 2315 | Beckman Coulter Diagnostics Miami, FL Systems Engineer II Master's degree in Engineering (ME, EE, Biomedical Engineer, Chemical Engineering or related technical subject area) Exp: 0+ years |
As a member of the R&D Hardware team, this role will report to the Manager, Systems Engineering responsible for development and sustaining of in vitro diagnostic products. If you thrive in a dynamic role and want to join an extraordinary R&D organization. | 10/22/2024 |
| 2316 | Beckman Coulter Diagnostics Carlsbad, CA Technician Production Operations Bachelor’s degree Exp: 0-1+ years |
The Reagent Formulations Technician for Beckman Coulter Diagnostics is part of a formulation team responsible for the manufacturing of reagents used in the medical diagnostics field. This role is critical to the healthcare industry and to allow doctors and lab technicians to diagnose patients quickly and accurately all over the world. This fully onsite position reports to the Supervisor for Aqueous Formulations and is part of the Production Operations Department located in Carlsbad, CA. If you thrive in a fast paced, detail-oriented role and want to work to build a world-class, quality focused manufacturing organization—read on. | 10/22/2024 |
| 2317 | Beckman Coulter Diagnostics Chaska, MN Quality Assurance Scientist I Bachelor´s degree in Science or Engineering related discipline Exp: 0-2 years |
The Quality Assurance Scientist I for Beckman Coulter Diagnostics is responsible for investigating customer complaints for the Immunoassay product line. This position is part of the Complaint Handling Unit located in Chaska, Minnesota and will be on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Post Market Surveillance organization and report to the Post Market Quality Assurance Manager responsible for ensuring complaints are correctly classified, records are populated per the current procedures and policies, and are investigated in a timely manner. If you thrive in a multifunctional role and want to work to build a world-class post market surveillance organization. | 10/22/2024 |
| 2318 | BD Zelienople, PA Manufacturing Quality Engineer B.S. or B.A. Degree in Science-related field, Quality Assurance, Engineering, Mathematics/Statistics or equivalent. Exp: 1 year |
The Quality Engineer performs various quality-engineering functions and associated support tasks in developing knowledge and experience in the areas of Quality Assurance. The role provides guidance for the various elements of the Quality System, for example, to ensure process control and identifies/recommends opportunities for continuous improvement (internal/external). Applies the appropriate statistical tools to analyze data, identify root cause and corrective actions for effective problem resolution of small to moderate in scope and complexity. May support both internal and external audits. | 10/22/2024 |
| 2319 | BD Mebane, NC Associate Quality Scientist Bachelor’s degree in Biology, Microbiology or other related Life Science Exp: 1-2 years |
Reporting to the Quality Scientist/Lab Supervisor, the BD Mebane Associate Quality Scientist is responsible for applying basic scientific principles to routine laboratory work, executing product testing, applying/interpreting scientific data of moderate complexity, ensuring good laboratory practices, and processing data generated from Quality Control testing. | 10/22/2024 |
| 2320 | BD Warwick, RI Product Development Engineer 1 Bachelor's degree in engineering or other applicable science field Exp: 1 year |
Direct project responsibility for design, development of new and improved products. Performance against schedule affects commitments made in the division business plan. Recommends product specifications, drawings, documents and changes as they pertain to any new products or product modifications. | 10/22/2024 |
| 2321 | Bend BioScience Bend, OR Analytical + Materials Scientist BS/BA in chemistry, pharmaceuticals, or related field Exp: 1-3 years |
Analytical and materials scientists will be responsible to progress programs collaboratively with multi-disciplinary teams by: Designing experiments tailored at challenging formulation attributes critical to successful formulation strategies. Performing materials characterization using expertise in analytical characterization to inform physical, chemical, and performance attributes for a range of formulation compositions. Running typical pharmaceutical analytical and materials science techniques for characterization (HPLC, GC, FT-IR, HPLC/UV, DSC, SEM, XRD). Efficiently interpreting results with a broad understanding of impact to formulation performance and robustness. Understanding and applying basic concepts of HPLC method development in support of early formulation work. Staying aware and current with pharmaceutical industry best practices in analytical chemistry. Demonstrating problem solving and troubleshooting ability related to routine procedures. Independently reviewing and interpreting complex analytical methods in support of formulation screening activities and implementing them in the lab in a timely manner. Independently documenting lab work in protocol, reports, and other required documentation. Ensuring preparation and timely delivery of data in support of formulation and manufacturing projects. | 10/22/2024 |
| 2322 | Bend BioScience Bend, OR Analytical scientist BS/BA in chemistry, pharmaceuticals, or related field Exp: 1-2 years |
Analytical scientists will be responsible to progress programs collaboratively with multi-disciplinary teams by: Analytical method development to support release of pharmaceutical intermediates and finished oral dosage forms including: HPLC, GC, FT-IR, PXRD, KF, and particle size. Understanding and applying basic concepts of HPLC method development in support of early formulation work Running typical pharmaceutical analytical techniques for characterization (HPLC, GC, FT-IR, KF, DSC, SEM, XRD, Particle Size). Demonstrating problem solving and troubleshooting ability related to routine procedures. Independently reviewing and interpreting analytical methods and implementing them in the lab in a timely manner. Independently documenting lab work in protocol, reports, and other required documentation. Ensuring preparation and timely delivery of data in support of formulation and manufacturing projects. | 10/22/2024 |
| 2323 | Bifrost Biosystems Berkeley, CA Mechanical Engineer BS or MS in Mechanical Engineering or a related field. Exp: 0-4 years |
Are you passionate about pushing the limits of technology to advance our understanding of the life sciences? So are we! We’re looking for a highly motivated and experienced Mechanical Engineer to join a fast-paced start-up developing tools that will transform functional cell biology research. The ideal candidate will have strong engineering and problem-solving skills, a solid grasp of mechanical design fundamentals and some exposure to optical systems, microscopy and bio-engineering or biology. As Mechanical Engineer, you will be part of a small team designing, developing, specifying and testing Bifrost’s hardware products. Additionally, you will play a role in product definition, development and verification testing. | 10/22/2024 |
| 2324 | Biocytogen Boston, MA Pharmacology Research Associate Bachelor’s or Master’s degree Exp: 1-3 years |
Biocytogen is a comprehensive research and discovery service provider for biotech and pharmaceutical industry and academic institutions. Its service platform integrates preclinical studies with innovative animal models, CRISPR-based gene editing, and animal supplies, with the current focus on immuno-oncology and oncology. We are looking for a highly motivated research associate with the ability to work both independently and collaboratively. Biocytogen is a fast-growing company and has an abundance of opportunities available for you to grow your career. Biocytogen is committed to nurturing junior scientists to progress within our organization, providing a supportive environment for career advancement. This opportunity is ideal for individuals who can recognize and seize learning opportunities. | 10/22/2024 |
| 2325 | BioEclipse Therapeutics Mountain View, CA Research Associate/Scientist BA, BS, or MS in Biology related field (Immunology, Virology, Hematology, Cell Biology, Microbiology, Molecular Biology, Biochemistry, etc.) Exp: 1-5 years |
Our R&D team is seeking a motivated Research Associate/Scientist to develop and perform assays central to the advancement of our novel immune therapeutic and to assist in the development of our platform. The person we are looking for is well organized, has good communication skills, and can work both independently and in multi-disciplinary teams. We are seeking candidates with experience working with pathogens, specifically viruses, who are proficient in cell culture, and ideally have GMP or process development experience. We are seeking candidates with hands-on laboratory experience such as cytotoxicity assays, quantitative PCR, flow cytometry, immunohistochemistry, and cell and virus harvesting. | 10/22/2024 |
| 2326 | Biofidelity Morrisville, NC Molecular Technologist II (2nd shift) Master’s degree in medical laboratory science or biological or chemical sciences Exp: 1+ years |
Biofidelity is seeking a Molecular Technologist II to perform high complexity diagnostic testing using Biofidelity’s ASPYRE technology, histology, and nucleic acid extraction workflows. With minimal oversight from the Supervisor, the Molecular Technologist II will be responsible for the efficient and quality execution of sample accessioning, processing, data generation, and reporting in the clinical laboratory. The ideal candidate has strong molecular biology technical skills, is collaborative, trustworthy with ability to work in a fast-paced clinical environment. This role reports to the Molecular Tech III, Team Lead. | 10/22/2024 |
| 2327 | BioMérieux Hazelwood, Mo Final QC Technical Lab Lead Bachelor’s Degree in Biology, or other equivalent discipline Exp: 0 years |
Provide direction to the Lab team including communicating lot status and priorities to the group and demonstrating good aseptic lab practices. Prioritize lab tasks to ensure the schedule is met. Assists and trains others as needed in performing and documenting testing. In addition, the position is responsible for ensuring proper documentation according to cGMP’s and current procedures. Using good aseptic lab practices, it supports performance testing and physical inspections of finished good lots and internal use only lots through set up of VITEK2 cards, to completion. | 10/22/2024 |
| 2328 | AstraZeneca Frederick, MD Quality Control Analyst (Sun-Wed) Bachelor’s degree in scientific/ biotech/ pharmaceutical or relevant field of study Exp: 0-3 years |
Join our Operations team as a Quality Control Analyst, where will be responsible for performing laboratory testing. This is an exciting opportunity to accelerate our Lean journey and take advantage of the huge opportunities to drive efficiencies in our processes and produce better-quality outputs. As a Quality Control Analyst, you will perform selected quality control testing activities, including raw materials, in process, finished product, and stability testing according to standard operating procedures. You will be responsible for conducting troubleshooting equipment problems, entering data evaluated for compliance to specifications, and reporting abnormalities. You will also be involved in writing new standard operating procedures or revising existing documentation. Your role will require you to apply critical thought to solving problems and work on problems requiring an in-depth knowledge of scientific methods and techniques. | 10/15/2024 |
| 2329 | AstraZeneca Santa Monica, CA Research Associate, Process Development MS degree in Immunology, Cell Biology, Molecular biology, Bioengineering, or relevant degrees Exp: 6 months |
As a Research Associate, you will manage process development studies to develop, optimize, scale-up and transfer cGMP manufacturing processes. You will carry out flow cytometry and cell-based assay experiments for the characterization of and optimization of cell therapy manufacturing processes. You will also perform cell culture of T cells in multiple formats including flasks, bags, and bioreactors. Collaborating within the project team to interpret study results and contribute to technical discussions for subsequent study design is also part of your role. You will prepare and review experimental proposals, technical reports, SOPs and manufacturing batch records. Working collaboratively within PD group and cross-functionally with other groups to meet Technical Operation organization goals is essential. | 10/15/2024 |
| 2330 | AstraZeneca Santa Monica, CA Associate, Quality Control Analytical Master's degree in Biological Sciences or related field Exp: 1 year |
We are looking for an energetic and experienced person with cell therapy quality control background to join our Quality Control (QC) team. You will contribute to the advancement of our product pipeline by performing QC analytical method qualification, complete sample analysis, and other assigned tasks. You will also independently organize and present results and conclusions. You will ensure that the QC Analytical laboratory is operating as expected. | 10/15/2024 |
| 2331 | AstraZeneca Mount Vernon, IN Validation Engineer Bachelor’s degree in Engineering, Chemistry, Biology, or Pharmaceutical Sciences Exp: 0-3 years |
As a Validation Engineer, you will perform installation and operational and performance qualification (IQ/OQ/PQ) of critical manufacturing equipment, facilities, and utility systems. Your responsibilities will include developing and reviewing qualification protocols and reports, coordinating system and equipment documentation collection, and executing protocols. You will also solve qualification and cleaning validation execution issues using critical analysis skills and develop sound, reasoned solutions and recommendations. | 10/15/2024 |
| 2332 | AstraZeneca Waltham, MA Scientists, ADC/RC Target Biology Masters degree experience in Biology, Oncology, Biochemistry, Pharmacology, Molecular Biology, Cell Biology, or a related field. Exp: 1+ years |
We are currently seeking a highly motivated Scientist (non-PhD) with strong scientific excellence and technical expertise in oncology research to join our ADC Biology and Development team at Waltham, MA USA, within the Oncology Targeted Discovery (OTD) group. | 10/15/2024 |
| 2333 | AstraZeneca Gaithersburg, MA Associate Scientist, Late-Stage Formulation Sciences BS in Chemistry, Biochemistry, Pharmaceutical Sciences, Bioengineering or a related field Exp: 0-2+ years |
The Late-Stage Formulation Sciences (LSFS) Group is responsible for development of intended commercial formulations to advance AstraZeneca’s late stage biologics portfolio, and the life cycle management of commercialized products. The group plays an integral part in the design and development of patient centric drug products. As a part of Biopharmaceutical Development, the Late-Stage Formulation Sciences group, within the department of Dosage Form Design and Development, is on a mission to develop extraordinary products through excellent science, forward-thinking execution, and compassion for patients and those who touch our products. We develop and characterize intended commercial formulations and finished dosage forms to deliver high quality biologics to the market for patients. We develop robust formulations, Drug Products, and product control strategies to ensure approval of marketing applications for product commercialization and launch. | 10/15/2024 |
| 2334 | Andelyn Biosciences Columbus, OH GMP Quality Control Scientist I (2nd Shift) BS in the life sciences, biotechnology, or gene therapy industries Exp: 0 years |
The GMP Quality Control (QC) Scientist I will perform assigned tasks to support the daily operations of the GMP QC laboratory. The primary objective is to ensure that all activities within the GMP QC laboratory facility comply with the requisite regulations (21 CFR Part 211 Subpart I, 21 CFR Part 11, et. al.). Working in close collaboration with QC Management, and senior QC staff the Scientist I will aid all day-to-day lab operations, including project and timeline management, materials management, assisting with laboratory investigations, SOP generation and revision, and assay performance. The Scientist I will aid QC Management in ensuring that their assigned tasks are performed by following appropriate regulatory practices, analytical methods, and Standard Operating Procedures (SOPs) for GMP. | 10/15/2024 |
| 2335 | Andelyn Biosciences Dublin, OH Scientist II Master’s in the life sciences, biotechnology or gene therapy industries preferred Exp: No exp |
A Scientist II, in Process Devlopment, will support upstream and downstream process development activities including responsibilities in bioprocessing and analytics. Working in close collaboration with PD leadership and PD scientists, scientist II will support the execution and completion of projects involving platform development, optimization, in-process characterization, and tech transfer following appropriate regulatory practices, timelines, documentation, and standard operating procedures. Prior experience in the purification of biologics is preferred. He/She will keep abreast with state-of-the-art technologies and scientific advancements in the field and participate in discussions on scale-up of processes, process qualification, and strategies for process improvement. | 10/15/2024 |
| 2336 | Andelyn Biosciences Columbus, OH Quality Assurance Specialist I BS in the life sciences, biotechnology, or gene therapy industries Exp: 0 years |
The Quality Assurance (QA) Specialist supports the manufacturing operations by performing quality assurance functions for the GMP operations. The QA Specialist will be responsible for ensuring compliance with Good Manufacturing Practices (cGMP) regulations, policies, and procedures applicable to these areas. This position will report to the Quality Assurance Manager and will work closely with the manufacturing operations staff. | 10/15/2024 |
| 2337 | AngioDynamics Marlborough, MA Regulatory Affairs Specialist - Temp Bachelors Level of Degree in a scientific or technical discipline field of study Exp: 1-2+ years |
Responsible for determining the path to market for new and modifications to existing products in compliance with Regulations of intended market territory and for guiding teams on the required deliverables to support the Regulatory status of products distributed by AngioDynamics Inc. | 10/15/2024 |
| 2338 | Anika Bedford, MA QC Microbiologist I, Environmental Monitoring Bachelors Degree preferred Exp: 1-2 years |
The QC Microbiologist I, Environmental Monitoring will learn, understand, and perform routine entry level sampling of cleanrooms and utilities according to written procedures under cGMP conditions; as well as tasks involved with clerical and logistical laboratory tasks. | 10/15/2024 |
| 2339 | Anika Bedford, MA QC Microbiologist I, Environmental Monitoring BS in microbiology, biology or related science Exp: 1+ years |
Responsible for all microbiological and some analytical testing of production materials under GMP conditions. Responsible for process and equipment validation (autoclave and depyrognenation oven) in cooperation with Engineering and R&D (New Product Sterility and LAL validation.) | 10/15/2024 |
| 2340 | Ansh Labs Webster, TX Scientist Master’s degree in Biological/Chemical Sciences/Biotechnology or related area Exp: 1 year |
As a key member of the Manufacturing or R&D Department, this individual will provide critical scientific skills to assist in the development and scale-up of immunodiagnostic products on various platforms (microtiter based ELISA, magnetic particle based immunoassays, routine microbiology, biochemistry, and protein purification. | 10/15/2024 |
| 2341 | Ansh Labs Webster, TX Jr. Scientist Bachelor’s degree in Biological/Chemical Sciences/Biotechnology or related area. Exp: 1 year |
As a key member of the Manufacturing, Research & Development and Quality Control departments, this individual will provide critical scientific skills to assist in the development, scale-up and QC testing of immunodiagnostic products on various platforms (microtiter based ELISA, magnetic particle based immunoassays). | 10/15/2024 |
| 2342 | Applied Medical Rancho Santa Margarita, CA Electrical Engineer II Bachelor's degree in electrical engineering or related engineering Exp: 1-2 years |
As an Electrical Engineer II at Applied Medical, you will play a crucial role in designing, developing, and testing electrical systems and components for medical devices. You will collaborate with cross-functional teams to ensure that the electrical systems meet product requirements and comply with regulatory standards. Additionally, you will contribute to the troubleshooting and resolution of electrical issues, ensuring the safety and reliability of the medical devices. | 10/15/2024 |
| 2343 | Applied Medical Rancho Santa Margarita, CA Manufacturing Process Engineer II Bachelor’s degree in Mechanical, Biomedical, Industrial, or Manufacturing Engineering Exp: 1-2 years |
Collaboration is a fundamental part of our organization's culture and is essential to our continued success. As such, the successful candidate for this position is expected to work on-site, enabling them to engage fully with colleagues and contribute to cross-functional initiatives. Therefore, the ability to work collaboratively and contribute to a positive and supportive team environment is a key requirement for this role. As a Process Engineer II, you will use skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. | 10/15/2024 |
| 2344 | Applied Medical Rancho Santa Margarita, CA Process Engineer II/III Bachelor’s degree in Mechanical, Biomedical, Industrial, or Manufacturing Engineering Exp: 1-4 years |
As a Process Engineer, you will work within the Group Process Development team and use skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. The Process Engineer’s primary responsibilities are debugging, observing, and expediting shop orders. You will assist with developing and updating engineering documents and investigating new tooling, materials, manufacturing processes, and technologies. | 10/15/2024 |
| 2345 | Applied Medical Rancho Santa Margarita, CA Quality Systems Engineer I/II – Test Method Validation Bachelor's Degree or higher in Engineering or a scientific field. Exp: 1 year |
Join our innovative team as a Quality Engineer, where you will play a pivotal role in ensuring the highest standards of medical device safety and efficacy. Specializing in Test Method Validation, you will spearhead critical assessments to guarantee that our testing processes are precise, reliable, and compliant with regulatory standards. Your expertise will directly contribute to advancing healthcare solutions, impacting patient lives worldwide. | 10/15/2024 |
| 2346 | Aprecia Pharmaceuticals Blue Ash, OH Quality Analyst I B.S. degree in scientific discipline Exp: 1-2 years |
This position is primarily responsible for providing Quality support for manufacturing operations. Perform review of GMP documentation including manufacturing and packaging batch records, manufacturing logbooks, material specifications, and other quality documentation as assigned. Assist with ‘QA (Quality Assurance) on the Floor’ duties, including support for Manufacturing during production by providing room inspection and clearances, equipment inspection and clearances, and other quality checks required during the manufacturing and packaging processes. Writing and reviewing standard operating procedures and technical documentation for the storage, manufacture, testing, and distribution of products manufactured. Provide quality oversight, document review and guidance for other departments. Support other areas of Quality Assurance including Quality Systems and Quality Control, as designated by management. | 10/15/2024 |
| 2347 | Argonaut Manufacturing Services Carlsbad, CA Bioprocess Technician II Bachelor's degree in a related field Exp: 1 year |
The Bioprocess Technician is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The Manufacturing Technician is expected to fully participate in both departmental projects and any quality working teams which may be applicable. existing procedures. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. | 10/15/2024 |
| 2348 | Argonaut Manufacturing Services Carlsbad, CA Formulation Technician II Bachelor's degree in a related field Exp: 1 year |
The Formulations Technician is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The Manufacturing Technician is expected to fully participate in both departmental projects and any quality working teams which may be applicable. existing procedures. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. | 10/15/2024 |
| 2349 | Argonaut Manufacturing Services Carlsbad, CA Manufacturing Technician II Bachelor's degree in a related field Exp: 1 year |
The Manufacturing Technician is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The Manufacturing Technician is expected to fully participate in both departmental projects and any quality working teams which may be applicable. existing procedures. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. | 10/15/2024 |
| 2350 | ARL Bio Pharma Oklahoma City, OK Chemist I - Analytical Bachelor’s degree in chemistry or related science Exp: 1-2 years |
Join a company where you can make a difference from day one and help make the world a better and safer place. ARL Bio Pharma provides analytical and microbiological testing for the pharmaceutical industry. Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug manufacturers, and raw material suppliers bringing excellence to pharmaceutical sciences and making pharmaceuticals safer. This position is a fantastic stepping-stone for those with some basic experience looking to expand their career in the interesting world of the pharmaceutical industry. The Chemist I is responsible for utilizing established methods and standard lab equipment/instrumentation (HPLC, IC) to qualitatively and quantitatively analyze routine pharmaceutical substances and formulations. | 10/15/2024 |
| 2351 | ARL Bio Pharma Oklahoma City, OK Chemist I - Chemistry Bachelor’s degree in chemistry or related science Exp: 0-2 years |
This position assists in maintaining the cleanliness of the laboratory, the organization of supplies, reagents and standards. Additionally, this position provides a backup for the daily calibration and/or verification of the balances and pH meter when the Lab Technician is unavailable. The employee will have basic knowledge of commonly used laboratory concepts, practices, procedures and instrumentation and will perform tests commensurate with skill level with some supervision. | 10/15/2024 |
| 2352 | ARL Bio Pharma Oklahoma City, OK R&D Scientist I Bachelor’s degree in chemistry or related science Exp: 0-2 years |
The position requires the performance of variety of task including development and validation of analytical methods and qualitatively/quantitatively testing routine and non-routine client samples. This position requires knowledge of commonly used concepts, practices, procedures, and instrumentation (HPLC/IC) used in a chemistry laboratory. Research Scientist I work with direct supervision and reports to the lab supervisor. The Research Scientist I must be able to think and work independently, yet share ideas and work toward team goals. Ability to express thoughts in a clear concise manner both orally and written is also expected. Works to establish the ability to effectively prioritize and plan multiple work activities with varying deadlines and complexities. | 10/15/2024 |
| 2353 | Arraystar Rockville, MD Lab Assistant - Molecular Biology Bachelor’s degree in a relevant biological field. Exp: 1-2 years |
Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. Assist with the generation and updating of laboratory SOPs. Perform basic lab maintenance tasks such as ordering lab supplies, and keeping detailed lab records. Communicate with clients to obtain/verify information of their projects, orders or requests. | 10/15/2024 |
| 2354 | Arthrex Naples, FL Research Operations Specialist Bachelor’s degree required, preferably in life sciences related field. Exp: 1 year |
Manages with autonomy and independent judgement the daily activities of the Department of Orthopedic Research that supports critical operations and functions. Responsible for departmental strategic development and surgeon collaborations. Spearhead key inter- and intra-departmental initiatives. | 10/15/2024 |
| 2355 | AskBio Durham, NC QC Sample Coordinator Bachelor’s Exp: 1+ years |
The Sample Coordinator, reporting to the Lab Operations Manager in Quality Control, will be responsible for sample handling, management, and transport within the Quality Control and Analytical Development laboratories along with all procedures and processes governing sample activities. | 10/15/2024 |
| 2356 | Astellas Westborough, MA Quality Systems Engineer Masters degree Exp: 1+ years |
The Quality Systems Engineer role participates in the development and execution of key compliance functions within the larger GMP Quality Assurance department. This position indirectly supports ongoing manufacture of biological clinical trial materials by providing timely and compliant support for quality systems including Change Control administration, Calibration / Validation review, MasterControl system administration and workflow development, inspection management and hosting, internal auditing, supplier management, site Quality Council, quality metrics generation, and site-level compliance deliverables. | 10/15/2024 |
| 2357 | Astellas Seattle, WA Research Associate II, Molecular Analytics MS Degree Exp: 0-2 years |
We are seeking a highly capable, self-motivated Research Associate II for our Core Technologies Department. This individual will contribute to the molecular engineering for our gene edited Universal Donor Cells with activities focused on performing custom TaqMan based PCR assays. They will work as a key member on a fast-paced team to run molecular assays to characterize our proprietary Universal Donor Cells. | 10/15/2024 |
| 2358 | Astellas Westborough, MA Quality Assurance, Compliance Specialist MS Degree Exp: 0-2 years |
This member of the Quality Assurance team will perform critical QA compliance tasks in support of GMP manufacturing programs as AIRM moves through clinical trials and commercialization. The successful candidate will foster compliance across a broad range of Quality Assurance areas and will work closely with talented counterparts in the Manufacturing, Quality Control, and Materials Management teams to help ensure high quality standards and value delivery for our patients. | 10/15/2024 |
| 2359 | Astellas Westborough, MA QC Associate II, Raw Materials MS Degree Exp: 0-2 years |
Astellas, Westborough is seeking a highly motivated individual with strong organizational skills to join us as a QC Analyst II, Raw Materials. This position provides Quality Control compliance and release testing of raw materials used in the manufacture of Astellas cell therapy products in accordance with GDP/GMP guidelines. | 10/15/2024 |
| 2360 | Bio-Techne San Marcos, CA QC Specialist Bachelor’s degree in Biological Science, Chemistry, or related field. Exp: 1-5 years |
Responsible for performing QC testing for Value Assignment assays, QC release assays, stability, physical/visual inspections, any related QC function. Assists in the flow of product in the QC department. | 10/15/2024 |
| 2361 | Bio-Techne Minneapolis, MN Research Associate Bachelor’s degree in biochemistry, microbiology, biotechnology,?or equivalent Exp: 0-2 years |
This position is responsible for the growth of E. coli in a GMP (Good Manufacturing Practice) Lab, following GMP guidelines. This includes, but is not limited to GMP, AF (Animal Free Process), and other products used by pharma and IVD customers. This position manufactures E. coli clones using shake flask, or Bioreactors using a variety of techniques, software and equipment including, Bioreactors, Shake Flasks, Biosafety cabinets, Fume Hoods, Sterile Filters, Autoclaves, and centrifuges. All procedures and batch records follow GMP guidelines. | 10/15/2024 |
| 2362 | Bio-Techne Minneapolis, MN Advanced Research Associate Master’s degree in a biological science Exp: 0-2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins and monoclonal antibodies for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for production, media and supplement preparation, and additional duties as assigned. This position requires weekend work with a Tuesday - Saturday shift. | 10/15/2024 |
| 2363 | Bio-Techne Minneapolis, MN Research Associate, Mammalian Cell Culture Bachelor’s degree in a biological science Exp: 0-2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins and monoclonal antibodies for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for production, media and supplement preparation, and additional duties as assigned. This position requires weekend work with a Tuesday - Saturday shift. | 10/15/2024 |
| 2364 | Bio-Techne Wallingford, CT Quality Technician Bachelor of Science degree in relevant field Exp: 0-2 years |
The Quality Technician role is established to support the Simple Plex Consumables team in the Wallingford facility. Assists Quality Analysts and the QA team in our ISO compliant environment. Provides support for QC / QA activities including: hands-on evaluation of microfluidic cartridge products. | 10/15/2024 |
| 2365 | Bio-Techne Minneapolis, MN Research Associate, Protein Purification GMP Bachelor’s degree in biochemistry, biotechnology, or equivalent Exp: 0-2 years |
This position is responsible for purifying proteins and polyclonal/monoclonal antibodies in a GMP Lab, following GMP guidelines. This includes, but is not limited to GMP, ACFP, natural, and other products used by pharma and IVD customers. Purifies proteins and polyclonal/monoclonal antibodies by column chromatography, using a variety of techniques and equipment. Filter, aliquot, and bottling of product using aseptic techniques, and submits to bulk inventory. Documents batch records following GMP guidelines. | 10/15/2024 |
| 2366 | Bio-Techne Minneapolis, MN Manufacturing Technician Bachelors of science in biotech, chemistry, Biology, or engineering related field Exp: 0-3 years |
The successful applicant will work with other members of the reagent prep production team as well as a multidisciplinary team of engineers and scientists to support routine production activities for reagent formulation. | 10/15/2024 |
| 2367 | Atalanta Therapeutics Boston, MA Associate Scientist II/Senior Associate Scientist, Oligonucleotide Chemistry Bachelor's or Master'sdegree in Chemistry or related scientific discipline Exp: Bachelor's: 1 year Master's: 0-2 years |
The candidate will join a dynamic team responsible for the design and synthesis of oligonucleotides for Atalanta’s drug discovery programs. Successful candidates will have experience with modern laboratory equipment, and spectroscopic analysis, preferably in relation to oligonucleotides, as well as demonstrated ability to work as part of an integrated team on multiple parallel projects. This individual will be responsible for the independent operation and maintenance of instruments to synthesize, purify, and analyze chemically modified oligonucleotides as well as prepare samples for in vitro and in vivo studies. The ideal candidate is personable, organized, and thrives in a fast-paced environment. This role provides the right candidate with the opportunity to take on increasing responsibility over time within Atalanta’s Chemistry function. | 10/15/2024 |
| 2368 | Nestlé Health Science Bohemia, NY Associate Chemist (2nd Shift) Bachelor's Degree in Chemistry or closely relate discipline Exp: 0-4 years |
As an Associate Chemist, you will play a vital role in performing routine laboratory procedures. Your responsibilities will include conducting various tests and analyses under general supervision. To excel in this role, you should have a strong familiarity with basic laboratory equipment and techniques. Your focus will primarily be on conducting less complex testing and providing valuable support functions to ensure the smooth operation of the laboratory. This position offers a dynamic and collaborative work environment, where you will have the chance to work alongside a team of dedicated chemists. You will have the opportunity to enhance your skills and knowledge in a supportive setting. If you are passionate about laboratory work and are eager to contribute to our quality control efforts, we encourage you to apply for this exciting opportunity as an Associate Chemist. | 10/08/2024 |
| 2369 | Nestlé Health Science Savannah, GA Associate Process Project Engineer Bachelor's degree (Preferred mechanical, food or chemical engineering) Exp: 1+ years |
Learn and develop the skills in the design of processing and packaging equipment and manufacturing line taking into consideration the safety, quality and line performance. Provide technical inputs to team members and factory staff applying his/her academic subject expertise to practical applications at the manufacturing shop floor. Aid plant engineering to drive continuous improvement or capital projects from inception through all the stages feasibility and project handover. Assist in the implementation of Asset Maintenance Management systems, and other performance improvement activities to reduce improve line performance, reduce TDC and ensure compliance. | 10/08/2024 |
| 2370 | Nestlé Health Science Bohemia, NY Industrial Engineering Specialist Bachelor of Science degree in Industrial Engineering/Engineering Exp: 1-3+ years |
The Industrial Performance Engineer will be responsible for identifying and driving operational improvement and cost savings projects. Continuous improvement efforts will focus on making sustainable gains in reliability, quality, safety, cost, and delivery. Methods for achieving and sustaining improvements will be based Nestle Continuous Excellence and TPM fundamentals. The team member will need to collaborate closely with Operations and other internal partners to achieve the project objectives aligned with the NHS business needs. The team member will be responsible to carry out assignments of a broad nature while exercising considerable judgment and creativity. The team member needs to be able to carry out appropriate financial analysis to validate/support proposals and gain support of key stakeholders. | 10/08/2024 |
| 2371 | Nestlé Health Science Sudbury, MA Quality Associate Bachelor’s Degree in a Science field Exp: 1 year |
Review all paperwork issued by Quality Associate before release for Production Department. Oversee the quality of the products manufactured and sold. Assist Product QA Supervisor & Quality Director in development of quality control and quality assurance programs. | 10/08/2024 |
| 2372 | Ajinomoto Bio-Pharma San Diego, CA Microbiology Associate I - 2nd Shift Bachelor’s degree in a Life Sciences discipline Exp: 1-2 years |
We are currently seeking a Microbiology Associate I – 2nd Shift. This position is responsible for supporting manufacturing at Ajinomoto Bio-Pharma Services. The Microbiology Associate I may focus in a specialized area and provide routine analysis and testing according to standard operating procedures in any of the following areas: in process and final product testing and microbiology assays including TOC, conductivity, bioburden, endotoxin, and growth promotion | 10/08/2024 |
| 2373 | Ajinomoto Bio-Pharma San Diego, CA Drug Product Manufacturing Associate I Bachelors in a science or engineering discipline Exp: 0-2 years |
We are currently seeking a Drug Product Manufacturing Associate I who is responsible for executing GMP production of injectable pharmaceuticals by following all applicable SOP's. Manufacturing associates are responsible for preparing equipment and materials for GMP aseptic production and operating equipment such from glasswashers, autoclaves, depyrogenation ovens and automated filling machines. | 10/08/2024 |
| 2374 | Akoya Biosciences Marlborough, MA Research Associate II BA or MSc in Life Sciences Exp: 1 year |
As a Research Associate II, you will work in a dynamic, team-oriented environment and take part in developing multiplex fluorescent immunohistochemistry (IHC) Reagents products for use in cutting- edge research. The desired skillset for laboratory work includes the ability to perform conventional immunohistochemistry (IHC), antibody conjugation, assay development for multiplex fluorescent staining. The candidate will be responsible for antibody validation, staining protocol optimization, and image analysis. In this role, you must be able to perform the following tasks independently: experiment setup and execution, reagents preparation, data analysis and protocol troubleshooting. | 10/08/2024 |
| 2375 | Alamar Biosciences Fremont, CA Lab Technician, Quality Control Bachelors degree in a scientific field Exp: 1-2 years |
We seek a highly motivated Lab Technician, Quality Control to join a dynamic team of professionals in the Operations team to support our company mission. This position will be working in the Quality Control team to support incoming receiving & inspections, visual inspections, analytical testing, and laboratory and equipment maintenances activities. Seeking a professional that is a quick learner, organized, detail oriented, and can handle shifting priorities in a fast-paced and rapid growing company, while adhering to established protocols and procedures in compliance to ISO 13485/GMP requirements. | 10/08/2024 |
| 2376 | Alcami Morrisville, NC Manufacturing Technician I - 2nd Shift Bachelor’s degree Exp: 0-1 years |
The Manufacturing Technician I is accountable for results in a fast-paced environment and is responsible for maintaining product quality by supporting GMP operations of life-saving sterile injectable drug products intended for clinical trials and commercial distribution. The Manufacturing Technician I operates in alignment with established Standard Operating Procedures (SOPs) and approved Batch Records, which are developed in accordance with regulatory expectations and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employs acceptable cleanroom techniques while working in manufacturing/inspection environments and is expected to demonstrate proficiency in all department procedures and provide manufacturing updates to area supervision. | 10/08/2024 |
| 2377 | Alcami Morrisville, NC Manufacturing Technician II - 1st Shift Bachelor’s degree Exp: 1-2 years |
The Manufacturing Technician II is accountable for results in a fast-paced environment and is responsible for maintaining product quality by supporting GMP operations of life-saving sterile injectable drug products intended for clinical trials and commercial distribution. The Manufacturing Technician II operates in alignment with established Standard Operating Procedures (SOPs) and approved Batch Records, which are developed in accordance with regulatory expectations and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician II employs acceptable cleanroom techniques while working in manufacturing/inspection environments and is expected to demonstrate proficiency in all department procedures and provide manufacturing updates to area supervision. | 10/08/2024 |
| 2378 | Alcami Morrisville, NC Manufacturing Technician II - 2nd Shift Bachelor’s degree Exp: 1-2 years |
The Manufacturing Technician II is accountable for results in a fast-paced environment and is responsible for maintaining product quality by supporting GMP operations of life-saving sterile injectable drug products intended for clinical trials and commercial distribution. The Manufacturing Technician II operates in alignment with established Standard Operating Procedures (SOPs) and approved Batch Records, which are developed in accordance with regulatory expectations and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician II employs acceptable cleanroom techniques while working in manufacturing/inspection environments and is expected to demonstrate proficiency in all department procedures and provide manufacturing updates to area supervision. | 10/08/2024 |
| 2379 | Alcon Johns Creek, GA Senior Engineer Associate Injection Molding Engineer M.S. Exp: 0+ years |
We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As a Senior Engineer Associate Injection Molding, you will be trusted to research, plan, design, develop, optimize and maintain injection molding processes. This includes part design, tooling, injection molding equipment, process optimization, and molded part measurement systems. Applies knowledge of injection molding principles to improve part design, specify tooling and molding equipment, optimize molding processes and trouble shoot injection molding processes. | 10/08/2024 |
| 2380 | Alcon Fort Worth, TX Senior Scientist M.S. Exp: 0+ years |
Developing new analytical methods and designing experiments that push boundaries of understanding. Advancing analysis of starting materials, in-process materials and finished products, ensuring the highest quality at every stage Documenting experiments, preparing technical documents, writing sections of regulatory documents and communicating and collaborating with colleagues and supervisors. Participating in functional teams and lab meetings offer assistance to co-workers and possibly leading a functional sub-team as expected. Applying chemistry and analytical technical skills to complete assigned work and solves routine problems. Ensuring products meet stringent standards for eye care, designing multiple studies. | 10/08/2024 |
| 2381 | Alcon Johns Creek, GA Senior Associate - Metrology M.S. Exp: 0+ years |
We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As a Senior Associate - Metrology supporting our Research and Development Engineering Team, you will lead and support metrology activities within the organization to ensure measurement accuracy and compliance with industry standards. You will be responsible for developing, implementing, and maintaining measurement systems, procedures, and equipment calibration processes at our R&D site in Johns Creek, GA. | 10/08/2024 |
| 2382 | Alcon Johns Creek, GA Validation Engineer M.S. Exp: 0+ years |
As a Validation Engineer supporting the U.S. Development of Characterization and Qualification Team in Duluth, GA. | 10/08/2024 |
| 2383 | Aldevron Fargo, ND Quality Control Environmental Analyst I Bachelor’s degree in microbiology or related scientific field Exp: 0-1 years |
This position is part of the Quality Control department located in Fargo, ND and will be an on-site position. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Quality Control Environmental Monitoring Team and report to the QC Environmental Monitoring Supervisor, and be responsible for sampling, detecting, quantifying, and identifying possible contaminants that may interfere with the quality of the product during the different stages of the manufacturing process. | 10/08/2024 |
| 2384 | Aldevron Madison, WI Associate Scientist II, R&D BS or MS degree in biology, molecular biology, biochemistry, chemistry, or related discipline Exp: BS: 1+ years; MS: 0+ years |
This position is part of the Research and Development Department located in Madison, WI and will be onsite. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Analytical Method Development team and report to the Senior Scientist responsible for analytical method development and new method research. | 10/08/2024 |
| 2385 | Alexza Fremont, CA Data Review I, Quality Control BS degree in scientific area or equivalent Exp: 0-2 years |
Perform timely data review with a high focus on data quality to ensure accuracy, completeness, cGMP compliance of QC test data. Verify data transfer, calculations and documented information such as reagent expiry, instrument calibration, logbook entries, standards, controls, etc. are present, complete and accurate. Verify that all analysis performed were as per test method and/or compendial methods and were in compliance with GMP requirements. Data review included but limited to QC testing data supporting product release, incoming material testing; stability studies, and qualification/validation/verification related studies. Complete training for test methods in a timely manner. Utilize knowledge of good documentation practices and good laboratory practices on a daily basis. Other duties as assigned. | 10/08/2024 |
| 2386 | AlivaMab Biologics San Diego, CA Research Associate II - Sequencing and Molecular Biology MS in Molecular Biology, Biomedical Engineering, or a related scientific field Exp: 1-3 years |
AlivaMab Biologics is seeking an outstanding individual to join the Antibody Engineering Team. The successful applicant will have the responsibility to support antibody discovery and engineering projects through Next-Generation Sequencing (NGS) of various samples including, but not limited to, hybridomas, single B-cells, immune repertoires, and phage libraries. The individual will also perform molecular cloning and contribute to technology development in the Molecular Biology group. This position will report to the Principal Scientist, Sequencing and Molecular Biology, and work closely with scientists in the Protein Sciences and Antibody Discovery teams. | 10/08/2024 |
| 2387 | Allogene Therapeutics Newark, CA Associate, Cell Therapy Manufacturing (Contract) Bachelors or Associates in relevant science or engineering discipline Exp: 0-2 years |
We are seeking a highly motivated Associate, Cell Therapy Manufacturing to join our Manufacturing team. This is a contract role. This role will work within the Manufacturing team in supporting our efforts in an exciting new area of cancer immunotherapy. This position is based out of Newark, CA. They will work within the Manufacturing team in supporting our efforts in an exciting new area of cancer immunotherapy. This position is based out of Newark, CA. The position will report to the Senior Manager, Manufacturing and will support the successful tech transfer and operational readiness process, using knowledge of cGMP regulations to ensure manufacturing readiness. Responsibilities of primary importance are: to ensure the successful, time-sensitive GMP manufacture and release of cell therapy products; to follow all processes and procedures related to operations in full compliance with cGMP, CFRs, site quality systems and company policies; and to promote a culture of quality and compliance. The successful candidate will have experience in a regulated biotech or pharmaceutical setting and will have proven competency and expertise in the GMP manufacture of cell-based therapies. | 10/08/2024 |
| 2388 | Alloy Therapeutics Waltham, MA Research Associate – Oligonucleotide Discovery B.S. or M.S. degree in Biology or related science Exp: 1-3 years |
As a Research Associate, you will work within the RNA Medicine team in Waltham, MA. You will also collaborate with internal/external partners on nucleic acid drug discovery projects to ensure timely execution of the experiments, and delivery of high-quality data. This role will have an autonomy owning various stakeholders, projects, and tasks in a dynamic start-up environment while keeping up the pace of Alloy. This is you! This role will report to our RNA Senior Scientist with autonomy owning various stakeholders, projects, and tasks in a dynamic start-up environment while keeping up the pace of Alloy. This is you! | 10/08/2024 |
| 2389 | Alltrna Cambridge, MA Senior Research Associate, Medicinal Chemistry MS degree in Chemistry, Biochemistry, or related discipline Exp: 1+ year |
We are looking for a passionate, creative scientist to join and our growing medicinal chemistry team focused on the advancement of our tRNA therapeutic platforms. This effort is driving forward a deeper mechanistic understanding of synthetic tRNA molecules. The successful candidate will join our highly innovative RNA/oligonucleotide synthesis team and have a strong background in oligonucleotide chemistry through hands-on experience in the synthesis, downstream process, characterization and purification of oligonucleotides. This individual would be part of the team that writes the textbook for developing tRNA molecules for therapeutics and be critical not only in ensuring that we can understand how our tRNA molecules are synthesized using automated systems but also in defining how we support our drug discovery and development efforts. We operate in an open and inclusive learning environment and need nimble thinkers who can chart courses and plan experiments based upon the data that we generate together. | 10/08/2024 |
| 2390 | Almac Group Durham, NC QC Inspector Grade 1 Bachelor's degree with science background Exp: 6+ months |
Almac Group is currently seeking a Quality Control Inspector Grade 1 for our Durham, NC location. The Quality Control Inspector will inspect operational activities for compliance to cGMPs, Almac SOPs, and other written quality and customer standards. | 10/08/2024 |
| 2391 | Vertex Boston, MA Discovery Biology Senior Research Associate Master's Degree in biological sciences Exp: 0-2 years |
Vertex is building out a Discovery Biology group focused on fundamental human biology, pushing the frontiers of stem cell biology to pursue curative cell therapies in multiple disease areas. The Discovery Biology Senir Research Associate performs a variety of well-defined support functions and participates in research activities, including the development of human stem cell models and assays to evaluate targets and lead molecules for Vertex diseases. | 10/08/2024 |
| 2392 | Alstem Richmond, CA Research Associate B.S. or M.S. degree in Biochemistry, Molecular Biology or related discipline. Exp: 1 year |
ALSTEM, INC is a growing research biotechnology company located in Richmond, CA. ALSTEM is a nimble provider of tools specializing in virus packaging, genome editing, cell engineering and stem cells for life science research. ALSTEM is looking for a highly organized and energetic Research Associate with a B.S or M.S. degree to join its scientific team. The candidate will be responsible to work as a team at all levels which will include but will not be limited to product testing and QC, and custom service projects following SOPs and protocols to support customer workflows. | 10/08/2024 |
| 2393 | Altasciences Columbia, MO Associate Scientist- Lab Sciences MS in biological, pharmaceutical science or related field Exp: 1 year |
Are you an experienced candidate looking for a new opportunity and a growing and innovative company? Altasciences is looking for you. We need someone who can provide technical and scientific leadership in the area (e.g., spectrophotometry, chromatography, ligand assay, flow cytometry, molecular biology). Plan and executes projects, and identifies and acquires the necessary facilities, equipment and procedures for research projects by performing the below duties. | 10/08/2024 |
| 2394 | Altasciences Columbia, MO Research Associate Bachelors degree in scientific discipline Exp: 1 year |
The Research Associate, Laboratory Sciences role assist in daily activities and operation of the Laboratory Sciences department including equipment maintenance, stocking supplies and general cleaning. Support and perform data collection activities including qPCR, DNA isolation, ligand binding assays, and flow cytometry, as assigned. | 10/08/2024 |
| 2395 | AltPep Corporation Seattle, WA Senior Research Associate Master’s degree Exp: 1+ year |
We are seeking a meticulous and dynamic Senior Research Associate to join our translational chemistry team. As part of this role, you will be responsible for conducting and supporting laboratory research, ensuring the highest standards of quality and precision. Your contributions will be critical to the success of our research and development efforts, and you will have opportunities to work both independently and collaboratively within our innovative team. | 10/08/2024 |
| 2396 | Alvogen Norwich, NY Chemist I BS in Chemistry, Biochemistry, Microbiology or Biology or related discipline Exp: 0-3 years |
The Quality Control Chemist I: Performs routine testing to assess the conformance of raw materials, finished products, and/or stability samples to predetermined product specifications. Performs routine testing in conformance with approved procedures, accurately and concisely documents data, and reports results. Demonstrates a basic knowledge of SOP’s and GMP regulations as related to the pharmaceutical quality control laboratory. | 10/08/2024 |
| 2397 | Amador Bioscience Pleasanton, CA Scientist - Bioanalysis & Biomarkers- LCMS Master’s, or Bachelor’s degree in biology, immunology, chemistry, pharmacology, or other related scientific fields Exp: 0-9 years |
Amador Laboratory Services Division specializes in bioanalysis (PK/PD/ADA), biomarkers, assay development & validation, and sample analysis. The team has successfully supported multiple non-GLP, GLP (nonclinical) and GCLP (clinical) projects. To meet the needs of business growth, we are looking for a highly motivated, experienced scientist/senior scientist to join our passionate team to partner with our clients for success. The successful candidate will be responsible for providing bioanalytical supports for both pre-clinical and clinical projects and will report to the Laboratory Head. | 10/08/2024 |
| 2398 | American Regent Brea, CA Validation Technician Bachelor degree in field of science Exp: Entry Level |
The Validation Technician will be responsible for supporting the qualification process of manufacturing equipment, facility utilities and storage chambers to ensure that all criteria satisfy FDA and cGMP guidelines for facility use. This position will also perform routine monitoring activities (such as routine monitoring of temperature-controlled chambers / areas and cleanroom pressure differentials) within the facility. | 10/08/2024 |
| 2399 | American Regent New Albany, OH QA Operations Associate I- 2nd Shift Bachelor’s Degree Exp: 1 year |
This position is responsible for ensuring the overall Quality in their assigned areas through the execution of site policies and procedures, programs and work instructions. Ensures all processes and products meet specifications and that products are produced in accordance with GMP requirements. | 10/08/2024 |
| 2400 | American Regent Columbus, OH QC Microbiologist I Bachelor’s degree in Microbiology, Biology, or equivalent Life Science curriculum Exp: 1 year |
This position in the Microbiology Laboratory will be primarily responsible for performing, coordinating and tracking the microbiological testing for in-process and finished products as well as monitoring of controlled manufacturing facilities and utility systems. | 10/08/2024 |
| 2401 | American Regent Columbus, OH Sterility Assurance Scientist I Bachelor’s Degree in Microbiology, Biology or related field Exp: 1 year |
This position in the Sterility Assurance Department will be primarily responsible for writing investigations/Excursions for Environmental and Personnel Monitoring with regards to assurance of sterility and being involved in technical projects from protocols to final reports. | 10/08/2024 |
| 2402 | Amgen Thousand Oaks, CA Sr. Associate (Process Development) Master’s degree in Chemical Engineering, Biomedical Engineering, Biochemistry, Biotechnology, Pharmaceutics or related subject area Exp: 1+ years |
Amgen is currently seeking a Process Development Senior Associate for our Pivotal Drug Product Technologies Group in Thousand Oaks, CA. This group is responsible for late stage drug product formulation and fill/finish process development for large molecule modalities (e.g. monoclonal antibodies, bispecific T-cell engagers (BiTEs) and fusion proteins). The Sr. Associate will work closely with a team of engineers and scientists responsible for the technical aspects of Amgen’s drug product commercialization and lifecycle management. | 10/08/2024 |
| 2403 | Amneal Piscataway, NJ Scientist II, Quality Control Master Degree (MBA) Chemistry or related science discipline Exp: 1+ year |
The Scientist II - QC is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. | 10/08/2024 |
| 2404 | Amneal Piscataway, NJ Scientist I, Quality Control Bachelors Degree (BA/BS) in Chemistry or related field Exp: 1 year |
The QC Chemist I (internally titled “Scientist I, Quality Control”) is an entry-level role responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents. | 10/08/2024 |
| 2405 | Amneal Brookhaven, NY Scientist I, Quality Control Bachelors Degree (BA/BS) in Chemistry or related field Exp: 1 year |
The QC Chemist I (internally titled “Scientist I, Quality Control”) is an entry-level role responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents. | 10/08/2024 |
| 2406 | Amneal Brookhaven, NY Validation Engineer I, Engineering Bachelors Degree (BA/BS) in Pharmaceutical manufacturing, Engineering, Science or relevant field Exp: 0-2 years |
The Validation Engineer I provides support in performing equipment, facility and utility qualification activity and re-qualification activity to ensure compliance to cGMP and Amneal's quality requirements. | 10/08/2024 |
| 2407 | Amneal Branchburg Township, NJ Scientist II, Quality Control Technical Services Master Degree (MBA) in Chemistry or related science discipline Exp: 1+ years |
The Scientist II - QC is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. | 10/08/2024 |
| 2408 | Abeona Therapeutics Cleveland, OH Quality Assurance Specialist, Supplier Quality Bachelor’s degree in related field Exp: 1 year |
The Specialist I, Supplier Quality will perform routine activities associated with manufacturing of cell and gene therapy products at the Abeona Therapeutics Inc. site in Cleveland, OH. This position supports the release of materials in support of cGMP Operations. The Specialist I, Quality Assurance will report to the Supervisor, Quality Assurance or above. | 09/30/2024 |
| 2409 | Abeona Therapeutics Cleveland, OH Quality Control Transport/Microbiology Associate BS in biology, microbiology, molecular biology or other relevant discipline Exp: 1-4 years |
The Quality Control Transport/Microbiology Associate assists in all aspects of Transport of Drug Products to treatment centers for the associated drug product. In addition, Transport associate will assist in Microbiology activities in support of GMP testing for Quality Control. Interacts with employees internal and external to Quality Control. | 09/30/2024 |
| 2410 | Abeona Therapeutics Cleveland, OH Sr. Associate, Manufacturing - Logistics QMS BS in life sciences, engineering, or other relevant discipline Exp: 1-4 years |
The Manufacturing Logistics QMS Senior Associate is responsible for working independently and with others to perform Quality Management System activities pertaining to the Manufacturing Department. This individual serves as an embedded quality assurance representative within the Manufacturing Department. | 09/30/2024 |
| 2411 | Abzena Bristol, PA Associate Scientist II, PD Chemistry B.Sc. in Chemistry or Chemical Engineering Exp: 1-2 years |
The Associate II will conduct research, troubleshoot, and solve problems arising during synthetic route/process development. The associate II will safely execute synthetic processes adhering to EHS and regulatory guidelines. | 09/30/2024 |
| 2412 | Abzena Bristol, PA Scientist I, PD Chemistry B.S or M.Sc. degree in Chemistry or Chemical Engineering Exp: 1-3 years |
The ability to design and conduct research, troubleshoot, and solve problems arising during synthetic route/process development. Develop safe and efficient synthetic processes that can be scaled-up reliably and reproducibly adhering to EHS and regulatory guidelines. | 09/30/2024 |
| 2413 | ICON Salt Lake City, UT Senior Laboratory Assistant Bachelor’s degree (preferred) Exp: 1 year |
We are currently seeking a Senior Laboratory Assistant to join our diverse and dynamic team at ICON at our Salt Lake City UT site. The Senior Lab Assistant aids the technical staff with the handling and storing of and accounting for biological lab specimens, quality control and any other relevant tasks. | 09/30/2024 |
| 2414 | Accurus Biosciences Richmond, CA Research Associate Bachelor’s degree in biology or a related field Exp: 0-3 years |
We are looking for a Research Associate to perform key tasks that are vital to our research services. The primary focus of this role involves molecular and cellular biology techniques, including DNA cloning, plasmid DNA preparation, site-directed mutagenesis, mammalian cell culture, cell transfection, stable cell line generation, FACS analysis, cell-based assays, and general lab maintenance. | 09/30/2024 |
| 2415 | Accutar Biotech Cranbury, NJ Medical Scientist (Drug Discovery Project Manager) Master in Medicine Exp: 1 year |
Coordinate and lead medical drug discovery clinical trial projects. Design and develop plans and process for specific drug during clinical trial process. Manage investigational product supplies and participate internal audits. Develop and review specific research-related documents. Develop and coordinate research project budget, management project progress and review project performance. Collect feedbacks and data from clinical trials and prepare reports for improvement of drug performance. Manage outsourced Central Lab activities. Serve as the contacts with partners and government agency in drug approving processing. | 09/30/2024 |
| 2416 | Accutar Biotech Mountain View, CA Senior AI Chemist Master’s degree in Chemistry or Chemical Engineering required Exp: 1 year |
Conduct qualitative and quantitative chemical analyses of lab data for our drug discovery pipelines with the assistance of developed artificial intelligence (AI) empowered platform. Write technical papers and reports. Prepare standards and specifications for operational protocols of drug discovery platform. Coordinate operations of company’s medchem lab. Coordinate the drug discovery projects within with outsourcing researcher and in house researchers. Collaborate with computation department to improve theefficiency, scalability and precision of our drug-discovery platform. | 09/30/2024 |
| 2417 | Acepodia Alameda, CA Research Associate I/II B.S. or M.S. in life science-related fields (Immunology, Molecular Biology, Pharmacology, Chemistry, and Biochemistry) Exp: Recent Graduate/Entry Level |
Acepodia is seeking a self-motivated and detailed-oriented individual with a passion for the translational research and pipeline development. This is an excellent opportunity for a recent graduate with a strong foundation in molecular biology and immunology to gain hands-on experience in a research and translational environment. The position involves both hands-on laboratory work and the translational activities essential to developing novel therapies. You will work in a supportive and collaborative cross functional team with R&D and clinical team members across the US and Taiwan. | 09/30/2024 |
| 2418 | AstraZeneca Gaithersburg, MD Associate Specialist Clinical Biologics Bachelor's degree Exp: 0-4 years |
As an Associate Specialist/Specialist in the Clinical production team within Biopharmaceutical Development, you’ll build broad knowledge of bioprocessing in a cGMP environment to launch your career in the biopharmaceutical industry. In this role you will take an adaptable, science driven approach to everything you do. You will become an integral part of process development, accelerating product candidates into the clinic and gaining knowledge and experience in cell culture, purification and critical support activities. Under the supervision of highly trained personnel, you will gain the process knowledge and skillsets to perform large scale clinical development activities. You will join a collaborative and driven team in an elite biopharmaceutical company. | 09/30/2024 |
| 2419 | AstraZeneca New Haven, CT Associate Scientist II, Injectable Drug Product Development Master’s degree in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or relevant Engineering/Life Sciences field Exp: 1+ years |
The Associate Scientist III will join Injectable Drug Product Development group to support the formulation and drug product process development of Alexion’s biotherapeutic candidates. This individual will lead and support execution of stability studies, develop fit for purpose analytical methods, perform analytical testing, and draft reports for the executed studies. This individual will work independently in a dynamic team environment and routinely collaborate with other members of Injectable Drug Product Development as well as other groups in Product Development and Clinical Supply. A general understanding of protein chemistry and machine learning based image analysis is preferred. | 09/30/2024 |
| 2420 | AstraZeneca Santa Monica, CA Associate, Quality Control Analytical Master's degree in Biological Sciences or related field Exp: 1 year |
Neogene is looking for an energetic and experienced person with cell therapy quality control background to join our Quality Control (QC) team. You will contribute to the advancement of our product pipeline by performing QC analytical method qualification, complete sample analysis, and other assigned tasks. You will also independently organize and present results and conclusions. You will ensure that the QC Analytical laboratory is operating as expected. | 09/30/2024 |
| 2421 | AstraZeneca Gaithersburg, MD Scientist, OTD Target Validation Master’s Degree in relevant discipline Exp: 1+ years |
We are seeking highly a motivated independent lab Scientist with wet-bench laboratory experience to join our Tumor Targeted Delivery team in Early Oncology in Gaithersburg, MD USA. As a Scientist, you will support target validation efforts for tumor-targeted therapies, such as antibody-drug-conjugates (ADCs) and targeted radio-conjugates. You will work collaboratively with cross-functional teams to advance pipeline programs and deepen our understanding of all aspects of target biology. | 09/30/2024 |
| 2422 | AstraZeneca Santa Monica, CA Senior Associate, Quality Control Microbiology MS/MA Exp: 1+ years |
We are seeking an individual with cell therapy quality control background to join our Quality team. You will contribute to the advancement of our product pipeline by performing environmental monitoring, lot release testing and other assigned tasks. You will also be expected to independently organize, analyze results, and present conclusions. You will ensure that the QC Microbiology Laboratory is operating as expected. | 09/30/2024 |
| 2423 | AstraZeneca Gaithersburg, MD Scientist in vivo - Immunology MS Exp: 1 year |
The successful candidate will be a key member of an in vivo team within the Early Respiratory & Immunology in vivo Department, performing in vivo and ex vivo studies to support a diverse range of immunology-related projects. This role specifically involves working as a lab-based scientist in the area of in vivo pharmacology. As a strongly self-motivated and independent individual you will be adept at working across functional areas, enabling you to maximize value from the available resources. The role will sometimes involve implementing protocols over timelines that extend outside of normal working patterns. The successful candidate will assist with the design, execution and analysis of experiments to generate data in support of pipeline projects. You will be expected to utilize your expertise to run various in vivo disease models, as well as provide input for the establishment of new in vivo models. | 09/30/2024 |
| 2424 | AstraZeneca Frederick, MD Electrical Engineer BA/BS in Engineering/Life Sciences Exp: 0-5 years |
As an Electrical Engineer, you will be responsible for a wide range of tasks including troubleshooting motor controls, performing BMS changes, supporting automation for electrical and utility systems, and implementing operational improvements to reduce energy consumption. You will also be involved in project management, problem-solving, and communication with internal teams and external vendors. Your work will contribute to the completion of milestones associated with specific activities and you will be expected to lead moderate cross-functional teams to complete work. | 09/30/2024 |
| 2425 | Adare Vandalia, OH Analytical Scientist I Master’s Degree in Chemistry or related discipline Exp: 0-1 years |
The will support the development and validation of analytical methods for raw materials, work-in-process, and finished products and to provide testing support for the formulation development and clinical supplies release process. The Scientist II will also be expected to provide some training, coaching, and mentoring for more junior scientists. This position reports to the Manager, Analytical Sciences, R&D. | 09/30/2024 |
| 2426 | Adare Vandalia, OH QC Chemist I - 3rd Shift Bachelors Degree in Chemistry or related field Exp: 1+ years |
The QC Chemist I is an essential part of the lab Quality team and will be expected to perform physical and chemical testing of intermediate and finished products according to written procedures. | 09/30/2024 |
| 2427 | Adesis Wilmington, DE Research Chemist Bachelor of Science Exp: 1-2 years |
Responsible for assisting chemists in performing various purifications of target compounds using various methods, including, but not limited to preparative high performance liquid chromatography (prep HPLC), normal phase and reverse phase chromatography, and recrystallization . | 09/30/2024 |
| 2428 | H.B. Fuller St. Paul, MN Scientist Master’s degree in chemistry or chemical engineering Exp: 1+ years |
The Scientist has primary responsibility for conducting research tasks coordinated by more experienced scientists and managers. In general, a Scientist conducts laboratory bench work tasks, physical testing and supports QA and Operations in trouble shooting manufacturing issues. This position is responsible for product development, cost saving initiatives, and production support. This person will be dealing primarily with moisture curing one-part and solvent free two-part technologies for adhesives, sealants, and coatings for the North America Construction Adhesives business. This includes building envelope, flooring, DIY, and other construction applications. | 09/30/2024 |
| 2429 | Adimab Lebanon, NH Research Associate - Molecular Biology B.S. or M.S. in molecular biology, cellular biology, biochemistry, or closely related field Exp: 1 year |
We are seeking an experienced Molecular Biologist to join our Antibody Library Team. The successful candidate will have prior experience in molecular or synthetic biology. The Research Associate will work in a small team to build our Antibody Library Platform. The associate will work closely with our antibody engineering and computational biology teams. | 09/30/2024 |
| 2430 | Adimab Lebanon, NH Research Associate - Antibody Engineering B.S., or equivalent practical experience, with training in molecular biology, chemical engineering, or biochemistry Exp: 1 year |
We are seeking a focused and enthusiastic protein engineer to join our Antibody Engineering group. The Research Associate will work in a small team setting, executing Adimab’s discovery platform on funded discovery and optimization projects and characterization of primary and optimized lead antibodies. | 09/30/2024 |
| 2431 | Admera Health South Plainfield, NJ Associate Scientist I/II (Lab) Bachelor’s or M.S. degree in Biological Sciences Exp: 1-3 years |
Admera Health is looking for an Associate Scientist I/II to join our growing team! Preparing solutions and reagents for performing assays on the bench. Perform Next Generation Sequencing-based genomic assays on different workflows (few listed below): o RNAseq o Whole Genome Sequencing o Whole Exome Sequencing. Carry out genomic assays under Biosafety Level II Policies and in regulatory compliance. Perform Operational Qualification and Performance Qualification on Next Generation Sequencers. Strictly follow standard operating procedures set forth for processing biological specimens while complying with laboratory safety protocols. Strict recordkeeping of all laboratory procedures. Continue acquiring next generation sequencing knowledge to support molecular biology techniques. Collaborate within the group and cross departmental to achieve goals. | 09/30/2024 |
| 2432 | Admera Health South Plainfield, NJ Project Specialist I M.S. in Biological Sciences Exp: 1-2+ years |
Admera Health is seeking a Project Specialist I to join our growing team! Admera Health provides genomic and bioinformatic services supporting discovery through clinical research stages. Our services include solutions for genomics, transcriptomics, epigenomics, and bioinformatics. Admera has deep expertise working with single-cell, FFPE, custom panels, and difficult or low-input samples. | 09/30/2024 |
| 2433 | B. Braun Medical Irvine, CA QC Chemistry Associate II (Chromatography) Bachelor's degree in a Science related field Exp: 1-2 years |
Perform routine laboratory analysis of In-Process, finished product, raw material, stability samples and environmental monitoring according to established specifications and procedures using wet chemistry techniques or various laboratory apparatus and instruments (e.g. HPLC, UV/Visible Spectrophotometer, FTIR, TOC, pH meter etc.) in compliance with B. Braun, cGMP, GLPs, SOPs, USP and FDA guidelines. | 09/30/2024 |
| 2434 | Affinia Therapeutics Waltham, MA Lab Technician, Analytical Development Bachelors degree in Biotechnology or related field Exp: 1-2 years |
Affinia Therapeutics is seeking an enthusiastic Lab Technician to join our Analytical Development laboratory team. As a member of the team, you will run analytic test methods for routine sample testing to support our process development and manufacturing activities. You will contribute to the evaluation of new analytical technologies and the development of more efficient laboratory workflows to maintain a culture of data quality and excellence. This position is located in our state-of-the-art facility in Waltham, MA. | 09/30/2024 |
| 2435 | Agathos Biologics Fargo, ND Laboratory Research Associate Bachelor’s degree in Biological Sciences or equivalent Exp: 1-5 years |
Agathos Biologics is seeking a Research Associate to join our team. The successful candidate will be responsible for following established protocols and conducting high-quality analytical testing. Attention to detail and accurate data reporting are crucial aspects of this role and important to the success of our company’s products and services. The ideal candidate will be highly organized, capable of working independently, and able to manage multiple projects simultaneously. | 09/30/2024 |
| 2436 | Agathos Biologics Fargo, ND Associate Scientist Bachelor’s degree in Biological Sciences or equivalent Exp: 1-5 years |
The Associate Scientist will conduct high quality scientific research and development to support the company’s goals and achieve their career objectives. | 09/30/2024 |
| 2437 | AGC Biologics Boulder, CO Quality Assurance Associate I Bachelor’s degree in biology, Chemistry or other relevant science/engineering discipline Exp: 0-2 years |
The Quality Assurance Associate I- III (In Plant Operations) is responsible for providing (24/7/365) Quality support to the activities listed below at the Boulder, CO site. One Colorado, one team. At our Boulder and Longmont locations, we cultivate a unified team under the banner of 'One Colorado', fostering collaboration among diverse teams and their respective business units. Together, we leverage a shared services objective between the two sites to enhance care for our clients and their patients. | 09/30/2024 |
| 2438 | AGC Biologics Boulder/Longmont, CO Downstream Manufacturing Associate I Bachelor’s degree Exp: 1 year |
The role of the Manufacturing Associate is to act as a controller, providing essential duties to support the respective production suite, Supervisor and Manager. On a daily basis, the Manufacturing Associate is expected to have a full understanding of the schedule and required tasks; promoting adequate assessment and response of any production demands. | 09/30/2024 |
| 2439 | AGC Biologics Boulder/Longmont, CO Upstream Manufacturing Associate I Bachelor’s degree Exp: 1 year |
The role of the Manufacturing Associate is to act as a controller, providing essential duties to support the respective production suite, Supervisor and Manager. On a daily basis, the Manufacturing Associate is expected to have a full understanding of the schedule and required tasks; promoting adequate assessment and response of any production demands. | 09/30/2024 |
| 2440 | AGC Biologics Bothell, WA Upstream Manufacturing Associate I BS/BA degree Exp: 0-2 years |
The role of the Manufacturing Associate is to act as a controller, providing essential duties to support the respective production suite, Supervisor, and Manager. On a daily basis, the Manufacturing Associate is expected to have a full understanding of the schedule and required tasks; promoting adequate assessment and response of any production demands. An Associate I assists with bioprocess operations in Manufacturing in compliance with established processes and standards. | 09/30/2024 |
| 2441 | AGC Biologics Bothell, WA Downstream Manufacturing Associate I BS/BA degree Exp: 0-2 years |
The role of the Manufacturing Associate is to act as a controller, providing essential duties to support the respective production suite, Supervisor, and Manager. On a daily basis, the Manufacturing Associate is expected to have a full understanding of the schedule and required tasks; promoting adequate assessment and response of any production demands. An Associate I assists with bioprocess operations in Manufacturing in compliance with established processes and standards. | 09/30/2024 |
| 2442 | Agilent Remote - Pearl River, NY Field Service Engineer Bachelor’s or master's degree within the science field - e.g., chemistry, analytical chemistry biochemistry, biotechnology Exp: 1-2+ years |
Every day, Agilent Regional Field Service Engineer help our customers to tackle issues that enable scientists to make discoveries that improve the quality of life. Through our work, we deliver insights and provide support that keep labs running smoothly and more efficiently. Join our multifaceted organization to be a part of this exciting work. As a Field Service Engineer for Agilent, you will work at a variety of labs, so having an appetite for continuously learning about new instruments, software and consumables is key. Applying your interpersonal skills, creativity and can-do attitude is essential. The ability to help with solving customer problems and a dedication to deliver the highest levels of customer service is how you will build customer success. | 09/30/2024 |
| 2443 | Agilent Boulder, CO Quality Control Analyst Bachelor’s Degree or equivalent experience in Analytical Chemistry or related life sciences field Exp: 1-3 years |
The Quality Control Analyst will conduct routine, non-routine analysis and review to support release, stability testing per Standard Operating Procedures (SOP) and Analytical Methods in accordance with current Good Manufacturing Practices (cGMPs) and regulatory requirements. Has a clear understanding of Good Laboratory Practices (GLPs), cGMPS, and other regulatory requirements. Effectively engages in continuous improvement of processes and procedures. Proven ability to exercise judgment and appropriately escalates issues to QC management. | 09/30/2024 |
| 2444 | Agilent Carpinteria, CA Research Laboratory Technician - Assays BS/BA in Biology, Biochemistry, or related field Exp: 0-2+ years |
We are looking for a hardworking and dedicated R&D Tech to join our CDx Research and Development Department. You will provide research support to develop accurate, robust, and precise assays. You will work in a cross-functional team dedicated to the design and development of CDx assays in a highly regulated environment. | 09/30/2024 |
| 2445 | Agilent Remote, TX Field Service Engineer Bachelors or Master’s degree within the science field - e.g., chemistry, analytical chemistry biochemistry, biotechnology Exp: 1-2+ years |
Every day, Agilent Regional Field Service Representative help our customers to tackle issues that enable scientists to make discoveries that improve the quality of life. Through our work, we deliver insights and provide support that keep labs running smoothly and more efficiently. Join our multifaceted organization to be a part of this exciting work. As a Field Service Representative for Agilent, you will work at a variety of labs, so having an appetite for continuously learning about new instruments, software and consumables is key. Applying your interpersonal skills, creativity and can-do attitude is essential. The ability to help with solving customer problems and a dedication to deliver the highest levels of customer service is how you will build customer success. | 09/30/2024 |
| 2446 | Agilent Cedar Creek, TX Manufacturing Scientist - Genomic Reagents Testing Bachelor's degree in Biological Science or a related field with chemistry, molecular biology, or biochemistry Exp: 1 year |
Join our innovative team at Agilent Technologies as a Manufacturing Scientist specializing in genomic reagents. You'll contribute to ground breaking products that advance Next Generation Sequencing (NGS), Microarray testing, and PCR-based technologies. If you're passionate about driving scientific advancements and thrive in a dynamic, collaborative environment, this role offers an exciting opportunity to grow and make a tangible impact. | 09/30/2024 |
| 2447 | Agilent Remote - Boston, MA Field Service Engineer - Biomolecular, Genomics, and Cell Analysis Instrumentation Bachelor’s degree within the science or engineering field – e.g. chemistry, analytical, biomedical Exp: 0-2 years |
As a Field Service Engineer for Agilent, you will work at a variety of labs, so having an appetite for continuously learning about new instruments, software and consumables is key. Applying your interpersonal skills, creativity and can-do attitude is essential. The ability to help with solving customer problems and a commitment to deliver the highest-levels of customer service is how you will build customer success. An Agilent Field Service Engineer supporting Biomolecular, Genomics, and Cellular Analysis instruments will travel to customer’s laboratories to install, maintain, and repair the Agilent instruments. These instruments are critical tools in the research, development, and manufacturing for several key areas including Cell and Gene Therapy, Infectious Disease, Virology and Vaccine Research, Immunology, Immuno-oncology, and Immunotherapy, as well as Next Generation Sequencing, and Pre-Natal Disease Detection. The Biomolecular Service Organization is an evolving and fast-growing part of Agilent’s Customer Service Organization supporting these growing and exciting markets. | 09/30/2024 |
| 2448 | Vivex Biologics Miami, FL IC/QC & Distribution Coordinator I Bachelors Exp: 0-1 years |
The IC/QC & Distribution Coordinator I - Weekend Shift is responsible for maintaining a high level of inventory accuracy and integrity within the Tissue Bank. Ensure that Inventory Control Operations are in Compliance with the State and Federal Regulations and AATB Standards. Promotes Lean Behaviors across the organization (This includes Participating in Try storming, Brainstorming and Lean Related Initiatives). Resourceful in completing deadlines and can multitask effectively. | 09/24/2024 |
| 2449 | Vivex Biologics Miami, FL Quality Assurance Engineer I Bachelor’s degree in engineering or a related technical discipline (e.g. Biology, Chemistry, etc.) Exp: 1 year |
The Quality Assurance Engineer develops, applies, revises, and maintains quality metrics to support areas of operations at Vivex Biologics, Inc. The role assists in the planning, development, implementation, communication, and maintenance of Vivex’s quality management systems, polices, documentation, data, and customer requirements. The Quality Assurance Engineer is expected to work with all departments to ensure compliance, that the final products are safe, reliable, and effective, and the successful and timely completion of projects. The Quality Assurance Engineer is mainly responsible for the maintenance of CAPA system items. They play a key role in preventing issues or fixing them if they arise by defining, monitoring, and approving the processes needed to achieve production standards. | 09/24/2024 |
| 2450 | Vivex Biologics Miami, FL Operations Processing Technician I Bachelor’s Degree in science or related Exp: 0-1 years |
The Operations Processing Technician I support the processing and documentation requirements of tissue during the cleaning, cutting, shaping, inspecting, and packaging operations for transplantation purposes. The Operations Processing Technician I is also responsible for ensuring that all equipment and supplies used for processing are maintained and ready for use, and that all Processing Room maintenance is completed daily while complying with Quality Assurance requirements as mandated by federal, state, and trade regulations. | 09/24/2024 |
| 2451 | Vivex Biologics Miami, FL Quality Control Labeling Inspector Bachelors Exp: 0-1 years |
The QC Labeling Inspector is responsible for maintaining a high level of inventory accuracy and integrity within the Tissue Bank. Performs final product labeling and inspections, manages transport and storage of quarantine tissue, and maintains labeling supplies. Promotes Lean Behaviors across the organization (This includes Participating in Try storming, Brainstorming and Lean Related Initiatives). Promotes Usage of Problem Solving. Ensure that Labeling Operations are in Compliance with the State and Federal Regulations and AATB Standards. | 09/24/2024 |
| 2452 | Vivex Biologics Miami, FL Inventory Control Coordinator I Bachelors Exp: 0-1 years |
The Inventory Coordinator is responsible for maintaining a high level of inventory accuracy and integrity within the Tissue Bank. Ensure that Inventory Control Operations are in Compliance with the State and Federal Regulations and AATB Standards. Promotes Lean Behaviors across the organization (This includes Participating in Try storming, Brainstorming and Lean Related Initiatives). Resourceful in completing deadlines and can multitask effective. | 09/24/2024 |
| 2453 | Vyriad Rochester, MN Quality Control Analyst Bachelor’s degree in a science related field. Exp: 1 year |
Responsible for performing and validating analytical methods essential for quality control and release of drug product. Performs environmental monitoring of critical manufacturing areas, thus ensuring that manufacturing processes and products meet quality specifications, under moderate direction of managers and senior team members. The analyst shall maintain quality assurance processes, be responsible for testing products, recording, and analyzing data during product development and manufacturing. The analyst will follow through on set processes and ensure adherence to best production practices and product quality standards, as well as monitors the efficiency and cost-effectiveness of product output. Receives general instructions on routine work and detailed instructions on new projects or assignments. | 09/24/2024 |
| 2454 | W. R. Grace & Co. Norco, LA Production Engineer B.S. degree in an Engineering discipline (Chemical Engineering preferred) Exp: 1-5+ years |
Grace is hiring a Production Engineer to join our Norco, LA manufacturing team. The Production Engineer will report to the Engineering Manager and be responsible for monitoring the production processes and ensuring safe and efficient operations to achieve the desired quality and production targets. The successful candidate needs to possess strong communication skills to effectively collaborate with other functional groups. | 09/24/2024 |
| 2455 | W. R. Grace & Co. Columbia, MD Sr Technician Specialist Bachelor’s degree in Science Exp: 1-2 years |
The primary function of this position is to support research activities in the Fluid Catalytic Cracking (FCC) catalyst product line. The typical daily activities of the employee will include: making laboratory/pilot scale preparations of FCC catalyst and additives, submitting samples for analysis and evaluation, keeping detailed records of the work performed, organizing and reporting results, monitoring the quality of the work and assisting in trouble shooting, and performing other assigned duties. Employee will work under general supervision of a research professional and as an integral member of the team. | 09/24/2024 |
| 2456 | W. R. Grace & Co. Baltimore, MD Technician Specialist, FCC BS/BA degree in technical field Exp: 1 year |
Grace is seeking a Technician Specialist to join our FCC Process Technology Team reporting to the FCC Process Tech Lead at the Process Innovation Center in Curtis Bay, Maryland. In this role, you will support Grace’s Special Material Request (SMR) program and assist in making laboratory/pilot scale preparations of FCC catalysts and additives. In the SMR program, an inventory of commercial plant production retains of a variety of grades is maintained and samples are prepared and sent to customers when they request them for exploratory or request for proposal (RFP) testing. Typical activities include drum handling, forklift operation, sample testing, sample packaging and preparing shipping paperwork. When engaged in preparing catalyst typical activities will include operating pilot scale equipment. | 09/24/2024 |
| 2457 | Wave Life Sciences Lexington, MA Scientist I/Scientist II, Pharmacometrics M.S. in clinical pharmacology, pharmacokinetics and metabolism, pharmacometrics, chemical/biomedical engineering, computational biology/chemistry or a Exp: 0-3 years |
Wave Life Sciences is seeking a creative, resourceful, and motivated pharmacometrician to join our organization to assist with and/or lead study design and data analysis for programs at various stages. In this role, you will support programs in the discovery, preclinical, and/or clinical stages spanning multiple modalities including RNA editing, splicing and silencing, as well as several disease areas. Strong communication skills and ability to work cross-functionally in a dynamic, fast-paced environment are required. This position is hybrid, you will be expected to work on site at our Lexington, MA facility. | 09/24/2024 |
| 2458 | Wilmington PharmaTech Newark, DE Research Chemists and Sr. Research Chemists B.A/B.S. or M.A./M.S. in Chemistry or Biochemistry Exp: 0-3 years |
Wilmington PharmaTech (WPT) is seeking self-motivated Research Scientists to join our dynamic chemistry process department for active pharmaceutical ingredient (API) synthesis in clinical phase drug development. | 09/24/2024 |
| 2459 | Worldwide Clinical Trials San Antonio, TX Assistant Clinical Research Coordinator Bachelor’s degree Exp: 1 year |
Clinical Research Coordinator Supervisor, and each clinical trial’s Principal Investigator, is responsible for assisting with assuring that the integrity and quality of the clinical research trial is maintained and that the trial is conducted in accordance with Good Clinical Practice guidelines and ICH guidelines as applicable. Teamwork and collaboration is paramount, especially as a globally distributed, remote based team. We are at the forefront of Worldwide’s exciting growth and the nexus between candidates and opportunities. | 09/24/2024 |
| 2460 | Worldwide Clinical Trials San Antonio, TX Clinical Research Coordinator 1 Bachelor’s degree Exp: 1 year |
Clinical Research Coordinator and each clinical trial’s Principal Investigator, is responsible for assisting with assuring that the integrity and quality of the clinical research trial is maintained and that the trial is conducted in accordance with Good Clinical Practice guidelines and ICH guidelines as applicable. Teamwork and collaboration is paramount, especially as a globally distributed, remote based team. We are at the forefront of Worldwide’s exciting growth and the nexus between candidates and opportunities. | 09/24/2024 |
| 2461 | Worldwide Clinical Trials San Antonio, TX Clinical Research Coordinator 1 Bachelor’s degree Exp: 1 year |
Clinical Research Coordinator and each clinical trial’s Principal Investigator, is responsible for assisting with assuring that the integrity and quality of the clinical research trial is maintained and that the trial is conducted in accordance with Good Clinical Practice guidelines and ICH guidelines as applicable. Teamwork and collaboration is paramount, especially as a globally distributed, remote based team. We are at the forefront of Worldwide’s exciting growth and the nexus between candidates and opportunities. | 09/24/2024 |
| 2462 | HD Biosciences, Inc. (Wuxi) San Diego, CA Research Associate II Bachelors in Biology related field Exp: 1-3 years |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology Division. We’re seeking a highly motivated Research Associate II to join the team. | 09/24/2024 |
| 2463 | HD Biosciences, Inc. (Wuxi) San Diego, CA Research Associate I - In Vivo Pharmacology Bachelors in Biology related field preferred Exp: 0-1 years |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly motivated Research Associate I to support our in vivo pharmacology team for various projects. | 09/24/2024 |
| 2464 | HD Biosciences, Inc. (Wuxi) San Diego, CA Research Associate I Bachelors in Life Sciences or related field preferred Exp: 0-1 year |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its Discovery Biomarkers team. We’re seeking a highly motivated Research Associate I to support our in vitro/ex vivo immunology team for various projects. | 09/24/2024 |
| 2465 | WuXi AppTec Philadelphia, PA Manufacturing Support Services Associate I Bachelor’s (science preferred) degree Exp: 0-2 years |
Responsible for the support activities and disinfection of GMP space, equipment and associated areas involved in the manufacture of Master and Working Cell Banks, within production facilities involved in the manufacture Cell & Gene Therapy products and final product fills according to current Good Manufacturing Practices (cGMPs). | 09/24/2024 |
| 2466 | WuXi AppTec Marietta, GA Associate Laboratory Technician Bachelor’s Degree Exp: 1 year |
Perform Sterility Testing in compliance with applicable Regulations, International Standards following SOPs in cleanroom type environment, perform QA/QC tasks, prep carts. | 09/24/2024 |
| 2467 | WuXi AppTec Philadelphia, PA Quality Control Environmental Monitoring Associate I Bachelor’s degree with a major in Biology, Microbiology, or related Life Science Exp: 0-3 years |
The Quality Control Environmental Monitoring Associate I is responsible for performing sampling and testing in support of manufacturing and validation activities, under the direction of a Supervisor or higher. Works in a team environment with various laboratory staff. | 09/24/2024 |
| 2468 | WuXi AppTec Philadelphia, PA Manufacturing Associate I - 2nd Shift Bachelor’s (science preferred) degree Exp: 0-2 years |
The Manufacturing Associate I is responsible for manufacture of Master and Working Cell Banks and performing activities within production facilities to support manufacture of Cell & Gene Therapy products, and final product fills according to current Good Manufacturing Practices (cGMPs). | 09/24/2024 |
| 2469 | WuXi Biologics Cranbury, NJ Associate Scientist, QC Testing - Raw Materials & Compendial Bachelor's degree Exp: 1+ years |
The QC Sampler Scientist is responsible for the quality and on-time delivery of samples, EM (Environmental sampling), laboratory inventory management to the various testing sections. This role will also ensure QC deliverables to internal departments and external clients are accurate and consistent. Demonstrates strong oral and written communication skills and actively contributes to training, report generation and GMP documentation. | 09/24/2024 |
| 2470 | Xilis Durham, NC Research Associate - Research & Innovation B.S. or M.S. degree in cancer biology, immunology, molecular biology or equivalent Exp: 1+ years |
The candidate will execute critical experiments in the laboratory to nurture and support Xilis' research and development team. Working very closely with thought leaders in immunology, cancer biology, and assay development, the candidate will process samples, gather data, keep meticulous notes, and participate in a detailed analysis, drawing conclusions, and formulation of next steps / experimental designs. The successful candidate will have a strong work ethic and bring exceptional skills to the laboratory with an ability to independently run complex experiments. He or she will have prior experience in primary cell culture, flow cytometry assays, molecular biology techniques, and a demonstrated ability to operate and maintain lab instrumentation and lab automation. Cross-functional team support and communication are central for this position. The candidate will report to the R&D program lead. By joining the team at an early stage, the candidate will have an outsized impact on fundamentally advancing precision cancer care therapy. | 09/24/2024 |
| 2471 | YMC Devens, MA Automation Engineer – Software Bachelor’s Degree in Chemical Engineering or Electrical Engineering preferred Exp: 0-2 years |
Automation Engineer will develop, implement, and test automation/control solutions for our products. This position is customer-driven and focused and is responsible for working with current and potential clients/customers. | 09/24/2024 |
| 2472 | BD Sparks, MD Quality Engineer II (Instrument Plant) MS in Mechanical or Electrical or Industrial Engineering, Biological Sciences, Chemistry, and/or Computer Science or other related field. Exp: 1 year |
The Quality Engineer II is responsible for the application and interpretation of the plant/department procedures to ensure consistency/compliance with Quality Systems. The Quality Engineer II uses the Company Quality Systems to ensure overall compliance and has the knowledge necessary to apply the appropriate statistical and analytical tools. Works with variable enterprise systems/Corporate directives to support new and/or current product lines and processes. Typical assignments may include, supporting one or more instrument platforms on sustaining items such as complaints, non-conformances and day to day issues, supporting audits, actively participating on teams, ensures documentation compliance, processing of CAPAs, change controls, and deviation waivers. Frequent interaction with other functional areas such as Research and Development, Operations, etc. is routine. The Quality Engineer II may take the lead in root cause investigations for issues of moderate complexity. | 09/24/2024 |
| 2473 | BD Covington, GA Lab Technician Bachelor’s degree in Biological Science (microbiology preferred) or related scientific discipline Exp: 1+ years |
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a maker of possible with us. | 09/24/2024 |
| 2474 | BD Sparks, MD Quality Engineer II, Chemistry MS in Biological Sciences, Chemistry, Engineering, Computer Science and/or Regulatory Affairs or other related field is required. Exp: No Exp |
The Quality Engineer is responsible for the application and interpretation of the plant/department procedures to ensure consistency/compliance with Quality Systems. The Quality Engineer uses the Company Quality Systems to ensure overall compliance and has the knowledge necessary to apply the appropriate statistical and analytical tools. Works with various enterprise systems/Corporate directives to support new and/or current product lines and processes. Typical assignments may include performing tasks, of moderate complexity, within planned schedules and timelines, test review for ROH release, water testing and OOS support, support for Validations of equipment and test methods, audits, actively participating on teams, ensuring documentation compliance, processing of CAPAs, change controls, and deviation waivers. Frequent interaction with other functional areas such as Research and Development, Operations, Facilities, etc. | 09/24/2024 |
| 2475 | Blue Life Solutions Irvine, CA Entry-Level Microbiology Associate Bachelor’s degree in microbiology, Biology, or a closely related field. Exp: Entry Level |
Blue Life Solutions, LLC is seeking a dedicated and detail-oriented Entry-Level Microbiology Associate to join our dynamic research team. The successful candidate will assist in conducting microbiological experiments, analyzing data, and maintaining laboratory equipment and records. This role offers an excellent opportunity for recent graduates to gain hands-on experience in a collaborative and innovative environment. This position is full time, fixed term (Duration: 2 years, with reevaluation for potential extension). | 09/24/2024 |
| 2476 | Zymo Research Tustin, CA Research Technician I- Epigenetics MS degree or a BS in Molecular Biology, Biochemistry, or related field. Exp: 1 year |
Zymo Research is seeking highly motivated individuals to join our epigenetics R&D team. The qualified individual will lead and execute R&D projects for product development, optimization, and quality control. As part of the epigenetics R&D team, you will leverage your skills and familiarity with a range of molecular biology assays, as well as data analysis expertise, to efficiently manage and develop innovative epigenetic and next-generation sequencing (NGS) products. The position is a full-time and fully onsite role based in our Zymo Research facility in Tustin, CA. | 09/24/2024 |
| 2477 | 89bio San Francisco, CA Clinical Trial Associate BA/BS in equivalent field Exp: 1+ years |
Reporting to our Associate Director of Clinical Operations, the Clinical Trial Associate will participate in planning and assisting in the managing the conduct of clinical trials in accordance with company policies and applicable regulations. The role may include some travel when conditions allow. | 09/24/2024 |
| 2478 | Abbott Temecula, CA Associate Engineer Manufacturing Bachelor's degree Exp: 0-2+ years |
Provides support to the Manufacturing organization to facilitate efficient operations within the production area, to optimize existing processes, and to ensure that production goals are met. Monitors performance of manufacturing lines, equipment, machines and tools and corrects equipment problems or process parameters that produce non-conforming products, low yields or product quality issues. Interfaces with Quality and other organizational functions to integrate new products or processes into the existing manufacturing area. | 09/24/2024 |
| 2479 | Abbott Sturgis, MI Assistant Chemist I, Analytical Lab, 2nd Shift Science related Bachelor’s Degree Exp: 1 year |
An Assistant Chemist I is responsible for testing the necessary raw ingredient, in process, and finished product as prescribed in the various quality procedures and assuring specifications and quality guidelines are met. The incumbent is responsible for producing the highest quality results while operating within the constraints of the manufacturing schedule and safety guidelines. They are responsible for maintaining good manufacturing practices and good laboratory practices. The chemist I is responsible for developing positive relations with other chemists and operators from other departments that interact with the laboratory. The incumbent is also responsible for providing timely feedback to the chemist following them, their lead chemist, and their supervisor as to the status of their area of responsibility. | 09/24/2024 |
| 2480 | Abbott Sunnyvale, CA Technical Services Engineer 1 Bachelors Degree - (Preferred Electrical Engineering, Biomedical Engineering ) Exp: 0-2+ years |
Functioning under general supervision, provides independent clinical and technical support in response to inquiries from physicians, health care professionals, patients and field staff using professional knowledge and judgment. This level of the Technical Service Engineer (TSE) provides the clinical and technical interface between the medical community and various departments through consultation. Requires the application of theoretical principles and creative/analytical techniques typically acquired in a recognized four-year or more biomedical engineering or other medical-related academic course of study. Identifies and routinely uses the most effective, cost efficient and best practices to execute processes; continually evaluates their effectiveness and appropriateness. Stays abreast of and consults on technical advancements. Promotes the process of continuous quality improvement and risk management, and coordinates solutions for technical and project issues. | 09/24/2024 |
| 2481 | Abbott Sylmar, CA Technical Services Engineer I Bachelors Degree - (Preferred Electrical Engineering, Biomedical Engineering ) Exp: 0-2+ years |
Functioning under general supervision, provides independent clinical and technical support in response to inquiries from physicians, health care professionals, patients and field staff using professional knowledge and judgment. This level of the Technical Service Engineer (TSE) provides the clinical and technical interface between the medical community and various departments through consultation. Requires the application of theoretical principles and creative/analytical techniques typically acquired in a recognized four-year or more biomedical engineering or other medical-related academic course of study. Identifies and routinely uses the most effective, cost efficient and best practices to execute processes; continually evaluates their effectiveness and appropriateness. Stays abreast of and consults on technical advancements. Promotes the process of continuous quality improvement and risk management, and coordinates solutions for technical and project issues. | 09/24/2024 |
| 2482 | Abbott Sturgis, MI Assistant Chemist I, Analytical Lab, 3rd Shift Science related Bachelor’s Degree Exp: 1 year |
An Assistant Chemist I is responsible for testing the necessary raw ingredient, in process, and finished product as prescribed in the various quality procedures and assuring specifications and quality guidelines are met. The incumbent is responsible for producing the highest quality results while operating within the constraints of the manufacturing schedule and safety guidelines. They are responsible for maintaining good manufacturing practices and good laboratory practices. The chemist I is responsible for developing positive relations with other chemists and operators from other departments that interact with the laboratory. The incumbent is also responsible for providing timely feedback to the chemist following them, their lead chemist, and their supervisor as to the status of their area of responsibility. | 09/24/2024 |
| 2483 | AbbVie North Chicago, IL Associate Scientist II Master’s Degree Exp: No Exp |
The Analytical Development group is responsible for programs that are transitioning from development stage to optimization and commercialization. We lead final method development, optimization, and validation, ensuring all analytical methods are fit for use in commercial QC laboratories. Key deliverables include product control strategies informed by analytical data and method understanding; robust analytical methods suitable for commercial QC labs; comprehensive data packages that drive product and process understanding; stability studies to establish commercial product dating; and approvable marketing application submission content. This position will work primarily inside of the laboratory, providing testing support to meet Analytical Development’s deliverables for pipeline programs. | 09/24/2024 |
| 2484 | AbbVie North Chicago, IL R&D Technician III BS Exp: 1+ year |
The R&D Technician carries out daily activities in the vivarium and will need to be proficient in humane rodent and dog handling skills, dosing by oral gavage, intravenous, and intraperitoneal routes, bleeding from the tail vein, assessing health, and performing humane euthanasia. The ideal candidate will also have postmortem examination (necropsy) experience. There are opportunities for expanding the candidate’s responsibilities beyond those identified as core job responsibilities. At all times, the candidate must adhere to the highest standards of animal welfare and personal conduct consistent with Abbvie values. The candidate will also be required to utilize a computer system to record all activities and observations. Ability to design, plan, organize and implement tasks within an allotted timeframe. Basic competence of Excel Spreadsheets, word processing, and email and knowledge of computerized maintenance management systems. The candidate will be required to work with potentially hazardous compounds, using appropriate precautions for the safety of the candidate and co-workers, and to prepare dosing formulations. | 09/24/2024 |
| 2485 | AbbVie North Chicago, IL Associate Scientist II, Analytical Chemistry Master’s Degree Exp: No Exp |
Within Small Molecule Chemistry and Manufacturing Control (CMC) Development, Analytical Research & Development focuses on utilizing measurement scientists of analytical chemistry to inform the development of new chemical entities and the associated formulations dosed in a preclinical and clinical setting across a wide range of pipeline programs. The group is highly cross-functional and works closely with internal Analytical R&D colleagues as well as colleagues within Discovery, Process Chemistry, Pharmaceutics and Drug Product Development. | 09/24/2024 |
| 2486 | AbbVie Irvine, CA Associate Scientist II, Pharmacology Master’s Degree Exp: 0+ years |
The Neurotoxin Research Group at Allergan/AbbVie is seeking a highly motivated and independent Associate Scientist II to join our Toxin Innovation Pharmacology Group. This individual will execute in vivo neuromuscular and sensory pharmacology studies, contributing to the design, execution, and communication of novel research in our highly collaborative neurotoxin discovery and innovation program. The successful candidate for this position will contribute to projects aimed at in vivo pharmacological characterization of biotherapeutics. He/she/they will be required to work on a variety of in vivo pharmacology models to help characterize and evaluate biological compounds. The successful candidate will organize, analyze, and interpret results, come forward with recommendations, and present the findings to senior personnel or in team meetings. Experience with rodent models is required. A background in neurobiology is highly desirable, but not required. | 09/24/2024 |
| 2487 | AbbVie North Chicago, IL Associate Scientist II or Scientist I - Process Chemistry Master’s Degree Exp: 0+ years |
Process Research and Development is responsible for inventing and executing the chemical processes and preparing active pharmaceutical ingredient (API) to enable clinical trials, toxicology studies and drug product development for Abbvie’s pre-clinical and clinical candidates. We create valuable intellectual property through composition of matter, chemical processes, and technology resulting in a cost-effective commercial manufacturing process. We develop the supply chain for APIs, prepare and defend CMC (Chemistry, Manufacturing and Control) regulatory content. We seek a highly motivated scientist with strong synthetic skills to work under the mentorship of a supervisor and to work in a multi-functional team environment. Opportunities may also exist to contribute to high-throughput experimentation, automation, and data science. | 09/24/2024 |
| 2488 | Tome Biosciences Watertown, MA Senior Research Associate, Analytical Development BS/MS in engineering, chemistry, biology, or other relevant degree Exp: 1-3 years |
Our Analytical Team is growing! Reporting to our Senior Scientist, Analytical Development, we are seeking a Senior Research Associate, Analytical Development to join our organization. In this role, the individual will perform various assays to analyze quality attributes of our lipid nanoparticles (LNPs), oligonucleotides and mRNA, with a focus on biophysical techniques. The individual will also contribute to method development to advance our knowledge in product attributes of these components. | 09/18/2024 |
| 2489 | Transpire Bio Miami, FL Associate Scientist I BSc in Chemistry, Pharmacy or related fields Exp: 0-2 years |
Conduct basic laboratory activities including for example analyzing raw materials, in-process materials and finished pharmaceutical products for quality, safety, purity, strength and identity using applicable methods or manufacturing drug product, following the cGMP, EH&S and other relevant guidelines of Corporate, FDA and other governing bodies. Set up and operate lab equipment. Prepare reagents, solvents and solutions for analytical and formulation activities. Prepare and maintain accurate records in lab notebooks of all tests performed. Process analytical data on lab equipment such as HPLC/UPLC, enter data in spreadsheets and conduct routine. calculations. Support the manufacture of inhalation drug products. Prepare samples for blend uniformity as required. Participate in project team activities and support project timelines and proactively contribute to meeting team objectives. Establish and maintain effective relationships with team members. Conduct lab work in accordance with SOPs & STPs; follow Corporate health & safety rules and procedures. Comply with Corporate guidelines and policies. | 09/18/2024 |
| 2490 | Transpire Bio Miami, FL Associate Scientist II MSc in Chemistry, Pharmacy or related fields Exp: 0-2 years |
Conduct basic laboratory activities including for example analyzing raw materials, in-process materials and finished pharmaceutical products for quality, safety, purity, strength and identity using applicable methods or manufacturing drug product, following the cGMP, EH&S and other relevant guidelines of Corporate, FDA and other governing bodies. Set up and operate lab equipment. Prepare reagents, solvents and solutions for analytical and formulation activities. Prepare and maintain accurate records in lab notebooks of all tests performed. Process analytical data on lab equipment such as HPLC/UPLC, enter data in spreadsheets and conduct routine. calculations. Support the manufacture of inhalation drug products. Prepare samples for blend uniformity as required. Participate in project team activities and support project timelines and proactively contribute to meeting team objectives. Establish and maintain effective relationships with team members. Conduct lab work in accordance with SOPs & STPs; follow Corporate health & safety rules and procedures. Comply with Corporate guidelines and policies. | 09/18/2024 |
| 2491 | TScan Therapeutics Waltham, MA Senior/Principal Research Associate, New Technology & Product Development M.S. in biology, immunology, pharmacology, or related field. Exp: 0-2+ years |
TScan Therapeutics is a clinical-stage biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for an experienced researcher to join our team as Senior/Principal Research Associate, supporting the New Technology and Product Development Team. The incoming candidate will have the opportunity to work at the intersection of biology and engineering to develop the next generation of TCR-T cell products. The ideal candidate should have relevant experience in T cell immunology, primary and tumor cell culture, cell-based assays, and flow cytometry, and enjoy exciting, collaborative and vibrant startup culture. A team player with a sense of urgency will thrive in this role. | 09/18/2024 |
| 2492 | Twist Bioscience South SF, CA Manufacturing Associate II, Library Production Bachelor in biology, chemistry, biochemistry, or similar disciplines preferred Exp: 1-3 years |
We are looking for an outstanding Manufacturing Associate II to join our Operations Team in South San Francisco, CA. The Manufacturing Associate II will produce a variety of DNA-based products with a focus on molecular biology techniques to meet production forecast and timelines and will assist research personnel with technology transfer to production. The candidate will be highly motivated, organized, willing to take initiative, and desire work in a highly collaborative environment. The ideal candidate will be eager to learn new techniques, have excellent molecular biology knowledge and skills, take detailed experimental notes, and communicate effectively with peers and management. | 09/18/2024 |
| 2493 | Twist Bioscience South SF, CA Sr Research Associate Bachelor’s or Master’s degree in Molecular Biology, Chemical Engineering, Biochemistry, Chemistry or closely-related field. Exp: 1-3 years |
We are seeking an outstanding Senior Research Associate to join our R&D team. The successful candidate will support R&D efforts in developing innovative nucleic acid-based applications and tools for synthetic biology and NGS products. This position will involve performing a range of experiments focused on development of protein expression and enzyme purification platforms. The ideal candidate will be very organized, have excellent molecular biology knowledge and laboratory skills, and communicate effectively with colleagues. | 09/18/2024 |
| 2494 | Unither Rochester, NY QA Operations Documentation Specialist BS degree in Life Sciences, Communications, Business Administration, Technical Writing, or related field is preferred. Exp: 1-3 years |
The QA Operations Documentation Specialist position provides documentation support aligned with commercial and development production. This position interacts with cross functional departments throughout the site to ensure all cGMP documentation is ready in advance of the schedule. The QA Operations Documentation Specialist is responsible for ensuring all necessary instructions and associated documentation is printed, verified and provided to the operations team. This position is also responsible for ensuring completed batch documentation is scanned into the system and sent to the customers. | 09/18/2024 |
| 2495 | Unither Rochester, NY Validation Specialist Bachelor’s Degree in Science or Engineering Discipline preferred. Exp: 0-2 years |
Manages validation projects or multiple validation project activities under limited supervision and performs assigned validation tasks such as validation product annual reviews and validated utilities re-certifications. | 09/18/2024 |
| 2496 | Astellas Pharma Seattle, WA Research Associate II MS Degree Exp: 0-2 years |
We are seeking a highly capable, self-motivated Research Associate II for our Cell Analytics, Core Technology Department. This individual will contribute to the characterization of our gene edited Universal Donor Cells, by utilizing various cell culture techniques. They will work as a key member on a fast-paced team to culture pluripotent stem cells as well as run cellular assays to characterize our proprietary Universal Donor Cells. | 09/18/2024 |
| 2497 | Vala Sciences San Diego, CA Research Associate (RA)/Senior Research Associate (SRA) – iPSC Manufacturing B.S. or M.S. in Cell/Molecular Biology, Biochemistry, Neuroscience, or related field Exp: 1-2 years |
We’re seeking an RA or SRA to join our dynamic induced pluripotent stem cell (iPSC) research and manufacturing program. The successful candidate will manage iPSC lines and their differentiation to different cell types, like cardiomyocytes, microglia, neurons, and astrocytes. These differentiated iPSC lines will be used for internal R&D projects, commercial research contracts, and manufacture for sale. You will evaluate and validate differentiated cell lines with biomarker detection methods like ICC or flow cytometry, and investigate and characterize cellular function using Vala’s live-cell fluorescent imaging technology. You will work in a close-knit, fast-paced team environment and adapt readily to changing needs as projects and technologies evolve | 09/18/2024 |
| 2498 | Vala Sciences San Diego, CA Research Associate (RA)/Senior Research Associate (SRA) – Assay Development and iPSC Maintenance B.S. or M.S. in Molecular/Cell Biology, Biochemistry, Neuroscience, Bioengineering, or related Exp: 1+ years |
We’re seeking an RA or SRA to join our dynamic assay development and induced pluripotent stem cell (iPSC) research team. The successful candidate will execute validated assays for contract research projects and assist in management and maintenance of iPSC lines. Additionally, you will work with senior scientists in the Neurobiology and Cardiology groups to plan and perform experiments for assay development to support Vala’s internal and contract research projects. You will maintain differentiated iPSC cell cultures for live cell assays using Vala’s Kinetic Image Cytometry (KIC) technology, as well as perform IF staining to assist in development of reproducible and optimized assays. You may perform differentiation of iPSC to different cell types, such as neurons, astrocytes, microglia and cardiomyocytes. You will work in a close-knit, fast-paced team environment and adapt readily to changing needs as projects and technologies evolve. | 09/18/2024 |
| 2499 | Beckman Coulter Life Sciences Remote - Chicago, IL Associate Field Service Engineer Bachelor's degree (B.S./B.A.) in mechanical, electrical, biological science, engineering Exp: No Exp |
The Service Technician is responsible for developing the knowledge and skills to support the maintenance, installation and repair of Beckman Coulter products at customer sites. This entry-level position works under close supervision and mentoring by a manager, regional specialist, and senior engineers within the territory. Tasks are performed independently as proficiencies are developed. This position is remote based in either Chicago, IL, Southern, IL, Milwaukee, WI, OR St. Louis, MO | 09/18/2024 |
| 2500 | Beckman Coulter Life Sciences Remote - Southern, IL Associate Field Service Engineer Bachelor's degree (B.S./B.A.) in mechanical, electrical, biological science, engineering Exp: No Exp |
The Service Technician is responsible for developing the knowledge and skills to support the maintenance, installation and repair of Beckman Coulter products at customer sites. This entry-level position works under close supervision and mentoring by a manager, regional specialist, and senior engineers within the territory. Tasks are performed independently as proficiencies are developed. This position is remote based in either Chicago, IL, Southern, IL, Milwaukee, WI, OR St. Louis, MO | 09/18/2024 |
| 2501 | Beckman Coulter Life Sciences Remote - Milwaukee, WI Associate Field Service Engineer Bachelor's degree (B.S./B.A.) in mechanical, electrical, biological science, engineering Exp: No Exp |
The Service Technician is responsible for developing the knowledge and skills to support the maintenance, installation and repair of Beckman Coulter products at customer sites. This entry-level position works under close supervision and mentoring by a manager, regional specialist, and senior engineers within the territory. Tasks are performed independently as proficiencies are developed. This position is remote based in either Chicago, IL, Southern, IL, Milwaukee, WI, OR St. Louis, MO | 09/18/2024 |
| 2502 | Beckman Coulter Life Sciences Remote - St. Louis, MO Associate Field Service Engineer Bachelor's degree (B.S./B.A.) in mechanical, electrical, biological science, engineering Exp: No Exp |
The Service Technician is responsible for developing the knowledge and skills to support the maintenance, installation and repair of Beckman Coulter products at customer sites. This entry-level position works under close supervision and mentoring by a manager, regional specialist, and senior engineers within the territory. Tasks are performed independently as proficiencies are developed. This position is remote based in either Chicago, IL, Southern, IL, Milwaukee, WI, OR St. Louis, MO | 09/18/2024 |
| 2503 | Vantage MedTech Lenexa, KS Process Engineer BS or MS degree in Engineering, preferably Mechanical or Manufacturing Engineering Exp: 1-3 years |
The Process Engineer will be responsible for ensuring that our innovative designs are transitioned into effective and sustainable production. Our life saving products are manufactured in Kansas City and require predictable delivery of high quality, cost-effective production over 5+ year product lifetimes. You will collaborate with Vantage MedTech’s Engineering and Manufacturing teams to provide input on the device design’s manufacturability, and plan and execute the transfer of these new products to our manufacturing facility. You will be responsible for ensuring that robust manufacturing processes are created, updated and in compliance with company standards, ISO and GMP as required. In addition, you will help drive improvement projects that impact quality and productivity. | 09/18/2024 |
| 2504 | Varian San Jose, CA Quality Incoming Inspections Engineer (Metrology Engineer) Master’s Degree Exp: 1 year |
As Quality Incoming Inspections Engineer you are expected to be able to perform assignments independently by applying Good Manufacturing Practices in all areas of responsibility to ensure our customers receive the highest possible quality products. This position is responsible for Incoming Inspection activities, interactions with internal customers to ensure parts are inspected in a timely manner in a FDA 21 QSR 820 and ISO 13485 regulated environment. You will need to perform all assigned duties and conduct business in a professional manner. | 09/18/2024 |
| 2505 | Variantyx Framingham, MA Analysis Preparation Scientist BS/BSc in a relevant field (Biology, Genetics) Exp: 1 year |
As a full time Analysis Preparation Scientist located in the US you will be responsible for the pre-interpretation step in our analysis process. | 09/18/2024 |
| 2506 | Vaxcyte San Carlos, CA Associate Scientist II, Analytical Development MS in Chemistry, Analytical Chemistry preferred, Organic / Biochemistry Exp: 1-4 years |
Looking for an energetic and talented individual to join our Analytical Development team. Primary responsibility for the incumbent will be to support the developmental activities currently on going in the laboratory as assigned. | 09/18/2024 |
| 2507 | Vector Laboratories Newark, CA Manufacturing Associate II, Library Production BS or BA degree in Chemistry Exp: 0-3 years |
The Manufacturing Associate I is primarily responsible for manufacturing Vector’s products according to established procedures and documenting all work in production batch records using established good documentation practices. The Manufacturing Associate I will operate and maintain common laboratory equipment as per instructions and works under general supervision on assigned tasks. Technical expertise should include strong knowledge of general laboratory safety and practices, basic knowledge of modern synthetic organic chemistry, multistep synthesis, and purification technique. This position will report to the Site Leader. | 09/18/2024 |
| 2508 | Adamson Analytical Laboratories Corona, CA Microbiology Laboratory Technician B.S. in Biology Exp: New Grads are welcome |
We are hiring for a Microbiology Lab Technician to join our Corona, CA team; Our ideal candidate will exhibit a passion for exploration and possess an insatiable curiosity! | 09/18/2024 |
| 2509 | Velocity Clinical Research Union, SC Clinical Research Coordinator I Bachelor’s degree in Science or Engineering Discipline preferred. Exp: 1 year |
The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs. | 09/18/2024 |
| 2510 | Velocity Clinical Research Albuquerque, TX Clinical Research Coordinator I Bachelor’s degree in Science or Engineering Discipline preferred. Exp: 1 year |
The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs. | 09/18/2024 |
| 2511 | Veloxity Labs Peoria, IL Associate Scientist II Bachelor’s degree in science (chemistry/biochemistry preferred) Exp: 1-2 years |
As an Associate Scientist II, you will be using state-of-the art technologies to perform bioanalytical testing for emerging pharmaceutical and biopharma companies. At Veloxity, we hire driven and motivated individuals and provide training and career advancement opportunities within our organization. | 09/18/2024 |
| 2512 | Veranova Devens, MA Senior Analytical Chemist BS in Chemistry Exp: 1-3 years |
The Senior Analytical Chemist is responsible for all project activities in ARD, including sample analyses and method development, transfer, and validation in a safe and reliable manner. This position requires the application of basic chemistry knowledge, as well as standard laboratory techniques and procedures. The Senior Analytical Chemist must also be able to make keen observations and learn how to solve more complex technical issues. | 09/18/2024 |
| 2513 | Veranova West Deptford, NJ Quality Control Chemist - Night Shift Bachelor's Degree in Chemistry or related field Exp: 1 year |
The purpose of the Quality Control Chemist is to perform chemical testing of in-process, raw materials, intermediates, and finished product samples in support of GMP production and stability testing. They execute standard analyses with regular supervision. | 09/18/2024 |
| 2514 | Veranova Devens, MA Analytical Scientist MS in Analytical Chemistry or equivalent Exp: 1 year |
Responsible for the design, development, qualification, validation, and implementation of analytical procedures in support of research, GMP production, and stability testing. The Analytical Scientist is expected to provide quality ideas and contribution to the assigned challenges; mentors junior analysts and offers recommendations and knowledge to other Veranova staff. | 09/18/2024 |
| 2515 | Veranova West Deptford, NJ Project Engineer Bachelor’s degree in chemical or mechanical engineering or equivalent degree required Exp: 1-5 years |
The Project Engineer is responsible for the safe and effective development, design, and implementation of assigned capital projects that are completed on time, on or below budget, with an end result that is fit for its intended purpose. Essential considerations are given to safety, quality, operability, processing efficiency, maintainability, and environmental compliance. The Project Engineer will also include participation in troubleshooting efforts, operation process support and continuous improvement. | 09/18/2024 |
| 2516 | Vericel Corporation Cambridge, MA Associate I, Cell Therapy Manufacturing Bachelor’s or higher degree (Life Sciences or related field) Exp: 0-2+ years |
Responsible for the execution of process steps to manufacture commercial cell therapy products meeting internal and regulatory requirements. | 09/18/2024 |
| 2517 | Vericel Corporation Cambridge, MA Associate II, Cell Therapy Manufacturing Bachelor’s or higher degree (Life Sciences or related field) Exp: 1-2 years |
Responsible for the execution of process steps to manufacture commercial cell therapy products meeting internal and regulatory requirements. | 09/18/2024 |
| 2518 | Vertex Pharmaceuticals San Diego, CA Molecular & Cell Biology Senior Research Associate Masters Degree (or equivalent degree) in biological science Exp: 0-2 years |
Join the cutting-edge team at Vertex Pharmaceuticals as a Senior Research Associate for Cell Biology in our Tissue Dissection Group. Our Molecular & Cell Biology (MCB) group in San Diego is seeking an outstanding Senior Research Associate to work in our tissue dissection function to generate high quality cells from primary human tissues for numerous Vertex research programs.The ideal candidate will have experience in human tissue dissection (especially DRG, lung, kidney & liver). This role will require the candidate to be reliable & flexible as donated tissues will require processing out-with normal working hours and during weekends. The ideal candidate will have the ability to drive method development & process optimization of dissection workflows. Familiarity with histological grossing & processing of tissues is a plus. | 09/18/2024 |
| 2519 | Vertex Pharmaceuticals Boston, MA Process Development Engineering Senior Scientific Associate Master’s degree in Biochemistry, Engineering, Biology or related discipline Exp: 0-2 years |
Vertex is seeking a talented Process Development Engineering Senior Scientific Associate to join our Process Development team. This individual will support the media development projects in cell and gene therapy applications, through a combined approach of fundamental hypotheses and high throughput screening and optimization. | 09/18/2024 |
| 2520 | Vertex Pharmaceuticals Boston, MA Pathology Senior Research Associate Master’s Degree in Biological Sciences or equivalent Exp: 0-2 years |
Preclinical Safety Assessment (PSA) is a global function responsible for the design and conduct of comprehensive nonclinical safety programs. Its pathology team supports animal model development and efficacy at all stages of discovery for the evaluation of candidate therapeutic agents. We are seeking a Senior Research Associate to perform histology techniques, data acquisition and compilation using state-of-the-art molecular pathology techniques to join our (PSA) team at Vertex. The incumbent will interface closely with other scientists, veterinary pathologists and histotechnologists in PSA as well as other cross-functional project teams to provide timely, high-quality data to support multiple projects across our drug development pipeline. | 09/18/2024 |
| 2521 | Sovereign Pharmaceuticals Fort Worth, TX QC Chemist I BA/BS Chem Exp: 0 years |
The primary function of a QC Chemist is to perform qualitative and quantitative chemical and physical analysis in support of raw materials, in-process samples, components, and finished drug products testing. | 09/18/2024 |
| 2522 | Sovereign Pharmaceuticals Fort Worth, TX QC Lab Technician BA/BS Chemistry Exp: 1-2 years |
Supporting QC Laboratory operations by performing, Documentation - most activities require proper documentation, Flexibility in prioritization of duties to ensure the QC Laboratory serves its internal and external customers | 09/18/2024 |
| 2523 | VGXI Conroe, TX Process Development Technician Bachelor’s degree Exp: 1-3 years |
Conduct research scale production of plasmid DNA on an ongoing basis. Perform and document routine maintenance on PD equipment. Assist the execution and analysis of data for the purpose of fermentation and purification process development. Assist the analysis of samples from cGMP seed banking, fermentation and purification processes. Assist experiments to evaluate new technologies as designed and supervised by senior team members. Maintain a clean and organized laboratory environment. | 09/18/2024 |
| 2524 | VIATRIS St. Albans, VT Chemist – 2nd Shift Bachelor’s degree Exp: 0-2 years |
Performs and documents the analysis of samples following approved test methods. Calculate, check, and/or review data. Assist with method development, validation, and transfer. Assist with instrument calibrations and maintenance. May work on analytical projects under direct supervision. Attend training classes and seminars as required. | 09/18/2024 |
| 2525 | VIATRIS Morgantown, WV Associate - LIMS Bachelor’s degree Exp: 0-2 years |
Provide Tier 1 support to the laboratory including answering questions and providing technical support to management and laboratory personnel as necessary. Assist with preparing LIMS stability studies for all incoming new product set downs, including both release and process validation samples. Assist with creation of LIMS Product Specifications, Item Codes, and related LIMS components for all new products. Assist with revising LIMS Product Specifications, Item Codes, and related LIMS components for all Specification changes. Apply LIMS Product Specification changes to existing samples in the Research and Development Chemistry laboratory. Assist with Stability Management duties as assigned | 09/18/2024 |
| 2526 | VIATRIS St. Albans, VT Chemist – 2nd Shift Bachelor’s degree Exp: 0-2 years |
Performs and documents the analysis of samples following approved test methods. Calculate, check, and/or review data. Assist with method development, validation, and transfer. Assist with instrument calibrations and maintenance. May work on analytical projects under direct supervision. Attend training classes and seminars as required. | 09/18/2024 |
| 2527 | VIATRIS Greensboro, NC Quality Compliance Associate Bachelor's degree Exp: 1-2 years |
Support the coordination, completion and documentation of site incident, investigation, complaint, and CAPA records to ensure timely closure of associated activities. Support the activities associated with the site’s data integrity document control and disposition activities. Support the operations related to the performance of the site internal inspection program. Review and/or revise SOPs and Work Instructions as they relate to internal and/or external inspections and incidents and investigations. Collect and report metrics associated with inspections and incident investigations for site Quality Council. Provide quality support during audits and inspections performed by customers, health authorities and/or regulatory agencies. | 09/18/2024 |
| 2528 | Stryker Remote, Customized Implant Design Engineer Bachelor of Science in Engineering, Mechanical Engineering, or Biomedical Engineering Exp: 0+ years |
Stryker is seeking to hire a Design Engineer to support Stryker Craniomaxillofacial (CMF) Division. This role has a direct impact on healthcare by designing customized patient implants. This is a remote role supporting the West Coast, and it requires working standard business hours in either the Pacific or Mountain Time Zone. | 09/11/2024 |
| 2529 | Sun Pharma Billerica, MA Microbiology Analyst I BS in Microbiology or relevant experience Exp: 0-2 years |
Performs GMP testing of raw materials, in-process and finished products, stability samples, and non-routine sample analyses per established procedures and methodology. | 09/11/2024 |
| 2530 | Sunbird Bio Cambridge, MA Research Associate BS or MS in biology, chemistry, biochemistry, or biomedical/chemical engineering or similar discipline Exp: 1-3+ years |
The Product Development team at Sunbird Bio's U.S. headquarters in Cambridge, Massachusetts, is searching for an innovative, motivated, and inquisitive Research Associate to help advance our neurodegenerative disease programs along the development pipeline. The ideal candidate will leverage their technical immunoassay experience to discover new biomarkers to further understand neurodegenerative disease signatures in blood samples. | 09/11/2024 |
| 2531 | BioDuro-Sundia Irvine, CA Scientist I, Formulation Development MS in Chemistry or related scientific discipline Exp: 1+ years |
The Scientist I, Formulation Development, assists in the design and development of drug delivery systems and dosage forms. | 09/11/2024 |
| 2532 | Sunflower Therapeutics Medford, MA Bioprocess Engineer Bachelor’s degree in chemical engineering or equivalent Exp: 1-3 years |
Sunflower Therapeutics is recruiting a motivated and highly organized individual to support its mission to deliver protein manufacturing solutions that anyone can use to create innovative new medicines, food products, and other bio-based products. Sunflower is advancing “right-sized” and ecient approaches to democratize protein manufacturing using strain engineering, integrated process development, and automated small-footprint facilities Reporting to the Director of Engineering Operations, the Bioprocess Engineer will be responsible for supporting engineering operations at Sunflower Therapeutics to enable the advancement of Sunflower’s protein manufacturing equipment prototypes. This individual will assist in the design, development, testing, and implementation of biomanufacturing systems for recombinant proteins. A successful candidate will be able to utilize bioprocess data to interpret product and process requirements and ensure the hardware design meets specified and operational standards. This individual will diagnose technical problems across system functions and suggest and carry out creative and timely solutions. As Sunflower grows, the Bioprocess Engineer will contribute to the continuous improvement of Sunflower’s automated multi-product protein manufacturing systems. | 09/11/2024 |
| 2533 | Adamson Analytical Laboratories Corona, CA Microbiology Laboratory Technician B.S. in Biology Exp: Entry Level, New Grads |
We are hiring now for a Microbiology Lab Technician to join our Corona, CA team; Our ideal candidate will exhibit a passion for exploration and possess an insatiable curiosity! | 09/11/2024 |
| 2534 | Synaptive Medical San Francisco, CA Clinical Applications Specialist Bachelor of Science degree Exp: 1-3 years |
The Clinical Applications Specialist (CAS) is an essential part of Synaptive Medical. The CAS provides primary on-site clinical support of Synaptive’s surgical technologies by acting as a knowledgeable and highly skilled technical resource in the hospital operating room. The CAS is expected to actively manage primary accounts assigned to them while also contributing to regional and national coverage as needed. At their assigned accounts, the CAS is responsible for driving customer engagement, supporting commercial success, pursuing excellence in clinical support, developing themself and the team, and maintaining good corporate citizenship. | 09/11/2024 |
| 2535 | Synaptive Medical Chicago, IL Clinical Applications Specialist Bachelor of Science degree Exp: 1-3 years |
The Clinical Applications Specialist (CAS) is an essential part of Synaptive Medical. The CAS provides primary on-site clinical support of Synaptive’s surgical technologies by acting as a knowledgeable and highly skilled technical resource in the hospital operating room. The CAS is expected to actively manage primary accounts assigned to them while also contributing to regional and national coverage as needed. At their assigned accounts, the CAS is responsible for driving customer engagement, supporting commercial success, pursuing excellence in clinical support, developing themself and the team, and maintaining good corporate citizenship. | 09/11/2024 |
| 2536 | SystImmune Redmond, WA Research Associate/Senior Research Associate BS or MS in immunology, biochemistry, molecular biology, structural biology, or a related field. Exp: 1+ years |
We are seeking a skilled Research Associate/Senior Research Associate with experience in utilizing display technologies (yeast/phage) in protein engineering, directed evolution, or binder discovery. This is a laboratory-based role that will be supporting protein engineering efforts in discovering novel binders and novel protein leads/scaffolds. The position will join a growing protein engineering team in an innovative organization and reports to the Director of Protein Engineering. The ideal candidate will be a quick learner with a broad experience set with direct expertise in a display technology and/or an adjacent field including but not limited to high throughput molecular biology, antibody/binder discovery, and protein engineering. Industry experience in biologics drug development is required. | 09/11/2024 |
| 2537 | Taconic Biosciences Rensselaer, NY Senior Lab Specialist Environmental Monitoring & Microbiology Bachelor’s degree within a science discipline Exp: 1 year |
If you ever wondered what is living on a door handle or if the hotel hot tub is full of bacteria, this opportunity may be the right one for you! We’re looking for a dedicated, motivated, and creative person who can help us carry out our mission: to create innovative solutions that both progress medical research and maintain the highest standards of laboratory animal care. The Senior Lab Specialist, Environmental Monitoring & Microbiology will be responsible for routine lot release testing, microbial evaluation of health and quality control samples as well as screening of various raw materials. Responsibilities also include data entry for lot releases and accessioning of test samples. This individual will also be the primary back-up for the Environmental Monitoring technician, whose responsibilities include scheduling, sample collection, sample analysis, microbial identification, data entry, and data review. This position is responsible and accountable for the accuracy of test results. | 09/11/2024 |
| 2538 | Taconic Biosciences Rensselaer, NY Senior Laboratory Specialist Molecular Analysis - 1st and 2nd Shift Bachelor’s Degree from a four-year college Exp: 1 year |
The Senior Laboratory Specialist performs a variety of molecular assays on animal samples and must be able to generate high-quality results in a timely manner. This individual should be comfortable working in a high-throughput environment and be able to use proper judgement to make technical decisions on assay performance issues. | 09/11/2024 |
| 2539 | Tactiva Therapeutics Buffalo, NY Senior laboratory technician Master's or Bachelor's Degree Exp: Master's: 18 months; Bachelor's: 30 months |
The senior laboratory technician performs specialized, technical scientific duties unique to research and development (R&D) for Tactiva Therapeutics. The senior laboratory technician designs and optimizes assay processes including sample preparation, workflow automation, and analytic detection, as well as provides data for critical review of test development. The senior laboratory technician provides direct scientific and analytic support to the laboratory director(s) and monitors timelines to meet production goals and objectives. | 09/11/2024 |
| 2540 | Takeda Boston, MA Associate Product Manager / Product Manager, Shared Platforms & Services BS/BEng in a technically relevant field of study (e.g. Engineering, Information Technology, Computer Science, Computer Engineering) Exp: 1-3 years |
Are you looking for a patient-focused, innovation-driven company that will inspire and empower you to shine? Join us as a Product Manager on the Shared Platforms & Services Team in Takeda’s Global Data, Digital, and Technology (GDD&T) team based in Cambridge, Massachusetts. The Shared Platforms & Services Team is a global team that allows Takeda to design, develop, and deploy externally facing digital solutions to patients and healthcare professionals (HCPs). Our team of software engineers and IT professionals share a passion for building trail-blazing digital solutions, while ensuring quality and compliance are followed to the highest standards. Our team works closely with local business teams, commercial, drug product teams, and research & development as key compliance enablers for both internal and external partners developing digital health solutions. The Product Manager will own the vision and product strategy for an internally facing compliance platform and the administration of Takeda’s digital asset compliance process framework. | 09/11/2024 |
| 2541 | Takeda Boston, MA Cell Therapy Data Engineer Master’s degree in Information Technology, Information Systems, Data Analytics, Engineering, Computer Science, or related field Exp: 1 year |
Takeda Development Center Americas, Inc. is seeking a Cell Therapy Data Engineer in Cambridge, MA with the following requirements: Master’s degree in Information Technology, Information Systems, Data Analytics, Engineering, Computer Science, or related field plus 1 year of related experience. Prior experience must include: Utilize computing languages including R, C/C++, Python, and Java; Apply knowledge in distributed computing, databases (e.g., SQL), relational databases (e.g., PostgreSQL), and Amazon Web Services; Demonstrate experience in database programming and development of dashboards; Demonstrate experience in data integration, programming, and the objective evaluation & utilization of analytical tools & libraries. | 09/11/2024 |
| 2542 | Takeda Social Circle, GA Sr QA Technician Bachelor's degree in scientific discipline Exp: No exp |
As the Sr QA Technician, you will be responsible for inspection of production materials, components, and chemicals to the Manufacturing facility. You will identify and assess regulatory and quality risks in activities and processes according to regulatory agency rules and guidelines and Takeda Quality practices. You will demonstrate effectiveness in task completion, decision-making and handling multiple projects. The hours of this position are 12PM-8:30PM, Monday-Friday; weekend and holiday work. Overtime may be required. | 09/11/2024 |
| 2543 | Takeda Boston, MA Senior Research Associate I, IVS Imaging Technician MS in a scientific discipline (or equivalent) Exp: 1+ years |
Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Senior Research Associate I, IVS Imaging Technician in our Cambridge, MA location. As a Senior Research Associate I, IVS Imaging Technician, you will perform complex animal manipulations for imaging procedures, supporting multiple therapeutic areas of the Company including Oncology, Drug Metabolism and Pharmacokinetics, CNS, GI and Imaging. You will also perform advanced dosing and biomethodology, sample collection, and animal procedures with efficiency, accuracy and attention to detail. As part of the Comparative Medicine team, you will report to Associate Director, Comparative Medicine and work with other groups within Preclinical and Translational Sciences. | 09/11/2024 |
| 2544 | Takeda Boston, MA Research Senior Associate, IBD/GI MS in a scientific discipline (or equivalent) Exp: 1+ years |
At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide. Join Takeda as a Research Senior Associate, IBD/GI, Inflammation Research where you will e part of a team focused on validation of novel targets and the evaluation of drug candidates for the treatment of chronic fibroinflammatory diseases. | 09/11/2024 |
| 2545 | Tanvex San Diego, CA QC Associate I, Lab Control BS in chemistry, biology, biochemistry or related life sciences discipline. Exp: 0-3 years |
The Quality Control Associate I, Lab Control is responsible for supporting the control and management of samples within QC and performing routine testing of in-process, release, and stability samples following written methods and procedures. The position will work as part of the Analytical Development (AD) / Quality Control (QC) group to support the team responsibilities. Adherence to GMP/ GDP guidelines and ability to follow SOP’s is required. | 09/11/2024 |
| 2546 | Tanvex San Diego, CA Manufacturing Associate, Upstream Bachelor's in life sciences or related discipline Exp: 0-3 years |
Under supervision, the Manufacturing Associate, Upstream, will perform routine manufacturing activities in GMP manufacturing areas including fermentation and/or cell culture, and the associated sub-processes/preparation. Operations will be performed according to Standard Operating Procedures (SOPs) and batch records. Perform manufacturing steps, execute routine batch records, and revise documents such as batch records and SOPs as needed. Flexible shift schedule and overtime may be required. | 09/11/2024 |
| 2547 | Tanvex San Diego, CA Manufacturing Associate, Downstream Bachelor's in life sciences or related discipline Exp: 0-3 years |
Under general supervision, the Manufacturing Associate, Downstream, will perform routine manufacturing activities in GMP manufacturing areas including purification and the associated sub-processes/ preparation. Operations will be performed according to Standard Operating Procedures (SOPs) and batch records. Perform manufacturing steps, execute routine batch records, and revise documents such as batch records and SOPs as needed. Flexible shift schedules and overtime may be required. | 09/11/2024 |
| 2548 | TE Connectivity Middletown, PA Technician IV Bachelor degree in related discipline Exp: 1-5 years |
The Appliances business is seeking to fulfill an engineering technician position to support engineering initiatives within the Appliance BU. The engineering technician will be primarily responsible supporting sample creation at the Middletown On-Wire lab. This position will require close coordination with our TE Engineering, Sales, and Product management teams to support new product development and expand sales. Other activities include and supporting the local engineering team with sample preparation, testing and analysis, fixture design, and shipping. | 09/11/2024 |
| 2549 | TE Connectivity Middletown, PA R&D Product Development Engineering BA/BS or MA/MS? Degree in ?Mechanical Engineering? or ?Electrical Engineering Exp: Entry Level, New Grads |
At TE Connectivity, you’ll help bring our purpose to life by creating a safer, sustainable, productive and connected future. In your role as a R&D Product Development Engineer in the Appliances Business Unit, you will help us make the connections that move the world forward by: Taking responsibility for supporting the development of new electrical connectors for the home appliances industry. Collaborating with senior engineers to collect requirements from customers, develop new concepts using 3D & 2D CAD, build prototypes, establish testing and validation plans, and work with operations to build tooling for mass production. | 09/11/2024 |
| 2550 | TE Connectivity Landisville, PA Controls Engineer Bachelor’s degree in electrical or mechanical engineering Exp: 0-3 years |
The focus of this position is to install machine safeguarding and control reliability safety systems on existing equipment. The ideal candidate will complete a quantitative risk assessment for manufacturing equipment and develop corrective actions that isolate the point-of-operation hazards and provide ISO category 3 safety circuit integrity. Secondary job duties include troubleshooting automated equipment involving programmable logic controllers, robotics, vision systems, pneumatics, and electrical instrumentations. | 09/11/2024 |
| 2551 | Tempus Durham, NC Molecular Technologist - Lead Trainer MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. Work closely with the Training Supervisor to schedule and execute training sessions with molecular team members according to the defined schedule. Routinely update checklists with training status, i.e. scheduled date of training, completion date of observations, side-by-sides, and competency assessments. Tailor training plans to individual team members, as appropriate, to ensure competency and confidence prior to initiation of clinical testing. Request competency modules in MediaLab and ensure completion and submissions per defined timelines. Review and update training materials, as needed. | 09/11/2024 |
| 2552 | Tempus Atlanta, GA Molecular Technologist I-IV BS or MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 0-2 years |
Work in a cutting-edge clinical laboratory to provide high-quality molecular test data with rapid turnaround times. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Able to identify deviations from established SOPS and apply routine fixes for known and common issues with standard solutions under direct supervision. Perform molecular techniques, which might include quantitative PCR, next-generation sequencing, nucleic acid extraction, DNA/RNA quantification and qualification or genotyping. Perform quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 09/11/2024 |
| 2553 | Tempus Chicago, IL Operations Specialist, Biological Modeling Lab Bachelors in Biological Sciences or Engineering. Exp: 1-3 years |
Tempus Biological Modeling is building the world's largest patient-derived organoid library to evaluate real-world data observations by constructing large scale data sets of molecular and experimental data. Tempus Biological Modeling is actively engaging with academic and industry partners in life science research, and we seek an Operations Specialist to accelerate our laboratory operations and academic research partnerships. | 09/11/2024 |
| 2554 | Tempus Chicago, IL Molecular Technologist (relocation assistance) BS or MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work in a cutting-edge clinical laboratory to provide high-quality molecular test data with rapid turnaround times. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Able to identify deviations from established SOPS and apply routine fixes for known and common issues with standard solutions under direct supervision. Perform molecular techniques, which might include quantitative PCR, next-generation sequencing, nucleic acid extraction, DNA/RNA quantification and qualification or genotyping. Perform quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 09/11/2024 |
| 2555 | Tempus Chicago, IL Molecular Technologist I BS or MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work in a cutting-edge clinical laboratory to provide high-quality molecular test data with rapid turnaround times. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Able to identify deviations from established SOPS and apply routine fixes for known and common issues with standard solutions under direct supervision. Perform molecular techniques, which might include quantitative PCR, next-generation sequencing, nucleic acid extraction, DNA/RNA quantification and qualification or genotyping. Perform quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 09/11/2024 |
| 2556 | Tempus Raleigh-Durham, NC Molecular Technologist I-IV: Sunday-Wednesday, AM Shift BS or MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work in a cutting-edge clinical laboratory to provide high-quality molecular test data with rapid turnaround times. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Able to identify deviations from established SOPS and apply routine fixes for known and common issues with standard solutions under direct supervision. Perform molecular techniques, which might include quantitative PCR, next-generation sequencing, nucleic acid extraction, DNA/RNA quantification and qualification or genotyping. Perform quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 09/11/2024 |
| 2557 | Tempus Raleigh-Durham, NC Molecular Technologist I-IV: Wednesday-Saturday, 2pm Shift BS or MS in medical technology, clinical laboratory science, chemical, physical or biological science Exp: 1 year |
Work in a cutting-edge clinical laboratory to provide high-quality molecular test data with rapid turnaround times. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Able to identify deviations from established SOPS and apply routine fixes for known and common issues with standard solutions under direct supervision. Perform molecular techniques, which might include quantitative PCR, next-generation sequencing, nucleic acid extraction, DNA/RNA quantification and qualification or genotyping. Perform quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Sterilizing laboratory equipment and workspaces as assigned. Entering clinical patient data into the Laboratory Information Management system. Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations. | 09/11/2024 |
| 2558 | Tessera Somerville, MA Engineer I/II, LNP Process Development Bachelor's or Master's degree in Chemical Engineering, Bioengineering, or Biological Sciences Exp: Bachelor's: 0-4 years; Master's: 0-2 years |
Tessera Therapeutics is pioneering Gene Writing™— a new biotechnology designed to offer scientists and clinicians the ability to write small and large therapeutic messages into the genome, thereby curing diseases at their source. Gene Writing holds the potential to become a new category in genetic medicine, building upon recent breakthroughs in gene therapy and gene editing while eliminating important limitations in their reach, utilization, and efficacy. Tessera Therapeutics was founded by Flagship Pioneering, a life sciences innovation enterprise that conceives, resources, and develops first-in-category companies to transform human health and sustainability. | 09/11/2024 |
| 2559 | Teva Pharmaceuticals Davie, FL MS&T Specialist II Master’s degree Exp: 1 year |
This position is responsible for performing activities related to critical aspects of products and processes, including process development, pre-validation and optimization of solid oral dosage forms after Abbreviated New Drug Application (ANDA) filing throughout product launch and commercial lifecycle including validation. Executes studies with Research and Development (R & D), Laboratory Technical Services (LTS), manufacturing and planning. Maintains of expertise related to formulation, raw material properties and manufacturing processes. Identifies, analyzes and suggests corrective actions to optimize procedures, processes, materials, technology and regulatory compliance issues. Provides direction and training to other staff, technicians and manufacturing operators. | 09/11/2024 |
| 2560 | TG Therapeutics Remote, NY Research and Development Associate BS/BA or MS/MA/PhD degree in a scientific discipline Exp: 1 year |
We are seeking a dynamic and proactive Research and Development Associate to join our Regulatory Affairs team. This role will be instrumental in supporting the various aspects of product development including nonclinical and clinical research. The ideal candidate will have a strong life sciences background, with a passion to build a career in the pharmaceutical industry. We are looking for a highly motivated individual, who can be a team player and an independent thinker. This role will report to the Associate Director, Regulatory and Development Strategy. We are looking to fill this role in the Summer of 2024. | 09/11/2024 |
| 2561 | Thermofisher Greenville, NC QC Scientist II (Lab Services) Master's of Science in Chemistry, Biochemistry, Biology, or related physical science. Exp: 1-2 years |
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or growing productivity in their laboratories, we are here to support them. You will make an impact to our society by ensuring drug products manufacture onsite are safe and have excellent quality by performing various tests in a GMP laboratory. | 09/11/2024 |
| 2562 | Thermofisher WardHill, MA Engineer III, QA Master’s degree or foreign degree equivalent in Mechanical Engineering, Industrial Engineering, or a related field of study Exp: 0 years |
Support SQM team and core SQM processes with onboarding of new suppliers and materials; Assign, track and reconcile GMP documentation; Support Quality activities for key processes including Vendor/Supplier Change Notifications (VCN/SCNs) and Supplier Corrective Action Requests (SCARs); Establish and implement Quality Technical Agreements with suppliers; Construct internal and external audits as well as regulatory inspections; Support supplier status changes as required to ensure that the Approved Supplier (Vendor) List is accurate and complete; and Maintain filing system for the supplier quality documentation. | 09/11/2024 |
| 2563 | Thermofisher Remote/Knoxville, TN Engineer II, Field Service - SEM/TEM/FIB University degree in electronics, physics, engineering, computer science or similar field preferred Exp: 1-5 years |
The Field Service Engineer II for the Materials and Structural Analysis Division (MSD) of Thermo Fisher Scientific is responsible for performing the on-site installation, servicing and repair of complex equipment and systems. Engineers investigate and improve operational quality of system equipment; Transmission Electron Microscopy (TEM), Scanning Electron Microscopy (SEM), Small/Large Dual Beam (SDB/LDB); instruct customers in the operation and maintenance of the system; serve as company liaison with customer on administrative and technical matters for assigned projects; and conduct on-site installations of the full range of Thermo Fisher Scientific electron microscopy systems and their associated options. | 09/11/2024 |
| 2564 | Thermofisher Greenville, NC Formulation Technician II Bachelor’s Exp: No exp |
The Formulation Technician II will be responsible to produce sterile injectables and work on problems of moderate scope where analysis of situations or data requires a review of a variety of factors. This colleague follows written and verbal instructions when performing the following duties. | 09/11/2024 |
| 2565 | Thermofisher Remote/Boston, MA Engineer I, Field Service Bachelor’s degree in engineering, biology, chemistry, or related field. Exp: 1-3 years |
The Field Service Engineer (FSE) performs customer installs, repairs and preventative maintenance on a variety of laboratory instruments in assigned territory. The FSE engages with customers and provides the highest quality of service in a professional and timely manner. | 09/11/2024 |
| 2566 | Thermofisher Grand Island,, NY Scientist I, Process Development, Cell Biology Bachelor's degree in Biology, Bioengineering, Biochemistry, Chemical Engineering or equivalent required. Exp: 3 months |
Discover impactful work in the scientist I role on our process development team. You will be exposed to an outstanding variety of cell types and bioreactor operating experiences. Working with a team, you will modify and implement study plans, assemble data, and assess workflows with a focus on teamwork and continuous process improvement. | 09/11/2024 |
| 2567 | Thermofisher Logan, UT Engineer II, Mechanical Master's degree in Engineering (mechanical or chemical) Exp: 1 year |
Thermo Fisher Scientific is seeking a motivated Sustaining Engineer to join our R&D engineering team in Logan, UT. As part our Bioproduction Group, you will have the opportunity to support the developers and manufacturers of biological-based therapeutics and vaccines. Drive process and product innovation by adapting both existing and novel single-use technologies. Support new and existing product development pipeline through collaboration with the R&D teams to generate new product ideas, evaluate existing product and evaluate new technologies for feasibility and application into bioprocess workflows. Drive activities, including hands-on and delegated testing, writing test plans and results, presentations, interpretation of data and collaborate multi functionally to meet the business needs. | 09/11/2024 |
| 2568 | Pfizer Andover, MA Associate Scientist BA or BS in biology, microbiology, or related field Exp: 0-2 years |
The qualified candidate will join the Analytical R&D Microbiology organization to enable development of biological therapeutics in Andover, MA. The qualified candidate will be responsible for applying GMP microbiological methods (bioburden, LAL, PCR, etc.) in the assessment of product quality and detection of impurities to support GMP in-process, release, and stability testing of clinical supplies. This group also performs micro method qualifications and Environmental Monitoring (EM) of Drug Substance and Drug Product facilities. The individual is responsible for becoming proficient in aseptic lab technique and facility gowning for EM in various GMP facilities (Cell Banking, Drug Substance, Drug Product) as well as facility water collection & testing, facility gas system collection & testing. Other assays may include bioburden, endotoxin, microbial identifications, media qualification, qPCR (e.g. MMV), and sterility testing. The colleague must work within corporate guidelines and must appropriately record, archive and report all data as this is a cGMP compliant laboratory. The colleague must be able to interact effectively with peers and leaders as part of a multi-disciplinary team. The candidate must thrive in a fast-paced environment. Attention to detail, strong organizational skills, the ability to multitask and effective interpersonal, influencing skills and communication skills are required. | 09/05/2024 |
| 2569 | Pfizer McPherson, KS Lab Analyst I Bachelors degree in Chemistry, Microbiology, Biochemistry, or related scientific field Exp: 0+ years |
The Laboratory Analyst I participate is enrolled in a defined training curricula to gain competency performing routine chemical, biological and or microbiological assays of engineering and/or commercial product raw materials, production bulk samples, finished product, environmental monitoring samples, process & cleaning validation samples, package samples and components. | 09/05/2024 |
| 2570 | Pfizer Kalamazoo, MI QC Laboratory Analyst II (Third Shift) Bachelor’s degree in Chemistry, Biochemistry or related science Exp: 0-1 years |
This position is for a testing analyst in the Kalamazoo Laboratory working on third shift. Opportunity for schedule flexibility exists as the Laboratory supports business and customer needs on weekends and holidays. Technologies employed in the Rapid Turn Laboratory include HPLC, GC, titrations, Karl Fisher, UV, and general analytical procedures. You will be developing and applying your knowledge of procedures, techniques, tools, materials and equipment. Your receptiveness to new ideas will enhance the team’s ability to achieve goals and targets. You will follow standard procedures to complete tasks and identify process issues or problems that involve direct application of your skills/knowledge. | 09/05/2024 |
| 2571 | Pfizer Andover, MA Manufacturing Process Engineer III Master's in Engineering Exp: 1+ years |
Working with Pfizer’s dynamic engineering team, you will play a critical role in developing and modifying process equipment, automation and controls to meet desired quality standards. Your production engineering skills will help in recommending and implementing improvements, modifications or additions that will help in solving problems. As an Engineer III, your focus on this job will contribute to achieving project tasks and goals. It is your domain knowledge, commitment, collaboration and dedication that will help us achieve new milestones and patients across the globe. | 09/05/2024 |
| 2572 | BioIVT Durham, NC Science Associate I Bachelor’s degree (B.S./B.A.) Exp: 1 years |
Under general guidance the Associate Scientist I will work as part of a team to conduct cell culture in support of research and product production goals and our customers need for high quality primary human cells and services. | 09/05/2024 |
| 2573 | LGC Clinical Diagnostics Gaithersburg, MD Quality Control Analyst I Bachelor's degree in a scientific discipline or equivalent Exp: 1-3 years |
The Quality Control Analyst I will support manufacturing activities, perform routine laboratory maintenance, and conduct routine sample preparations and analyses. Work environments will include typing/computer work at a desktop workstation, sitting and/or standing at laboratory bench, and working in biosafety cabinets and chemical exhaust hoods. | 09/05/2024 |
| 2574 | SGS Saint Rose, LA Laboratory Analyst I Bachelor’s Degree in a Chemistry or similar scientific discipline Exp: 0-2 years |
Prepare and analyze samples with accuracy and precision in accordance to SGS' analytical SOPs. Work independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. Understand and apply basic analytical chemistry principles. Always follow safe laboratory practices and maintain a safe working environment. | 09/05/2024 |
| 2575 | SGS Orlando, FL Laboratory Analyst I, Volatiles Bachelor’s Degree in a Chemistry or similar scientific discipline Exp: 0-2 years |
Prepare and analyze samples with accuracy and precision in accordance to SGS' analytical SOPs. Work independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. Understand and apply basic analytical chemistry principles. Always follow safe laboratory practices and maintain a safe working environment. | 09/05/2024 |
| 2576 | SGS Reno, NV Lab Analyst I Bachelor’s Degree in a Chemistry or similar scientific discipline Exp: 1-2 years |
Our Reno, NV laboratory is looking for an entry-level Laboratory Analyst to join their team! The Laboratory Analyst prepares and analyzes samples with accuracy and precision in accordance to SGS' analytical SOPs. The Laboratory Analyst works independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. The Laboratory Analyst understands and applies basic analytical chemistry principles. The Laboratory Analyst always follows safe laboratory practices and maintains a safe working environment. | 09/05/2024 |
| 2577 | SGS Las Vegas, NV Laboratory Analyst I Bachelor’s Degree in a Geology/Biology or similar scientific discipline Exp: 1-2 years |
Our Las Vegas, NV laboratory is looking for an entry-level Laboratory Analyst I to join their team! The Laboratory Analyst I prepares and analyzes samples with accuracy and precision in accordance to SGS' analytical SOPs. The Laboratory Analyst I works independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. The Laboratory Analyst I understands and applies basic microscopic principles. The Laboratory Analyst I always follows safe laboratory practices and maintains a safe working environment. | 09/05/2024 |
| 2578 | SGS Saint Rose, LA Chemist Bachelor’s Degree in Chemistry or a related science preferred Exp: 1 year |
Responsible for analysis and reporting of various products such as crude oil, fuel oils, middle distillates, petroleum and petrochemicals, LPG & LNG gases, etc. | 09/05/2024 |
| 2579 | SGS Anchorage, AK Laboratory Analyst Bachelor’s Degree in a Chemistry or similar scientific discipline Exp: 1-2 years |
Our Anchorage, AK laboratory is looking for a Laboratory Analyst to join our team! The Laboratory Analyst prepares and analyzes samples with accuracy and precision in accordance to SGS' analytical SOPs. The Laboratory Analyst works independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. The Laboratory Analyst understands and applies basic analytical chemistry principles. The Laboratory Analyst always follows safe laboratory practices and maintains a safe working environment. | 09/05/2024 |
| 2580 | SGS Deer Park, TX Chemist Bachelor’s Degree in Chemistry or a related science preferred Exp: 1 year |
Responsible for analysis and reporting of various products such as crude oil, fuel oils, middle distillates, petroleum and petrochemicals, LPG & LNG gases, etc. | 09/05/2024 |
| 2581 | Revvity San Diego, CA Biochemist II - Bacterial Cell Culture Bachelor of Science in Life Science or related area Exp: 6+ months |
This position is responsible for manufacturing cutting-edge recombinant protein research products in Molecular Cellular Immunology (MCI) group. The recombinant manufacturing associate will be involved in different stages of production of various recombinant protein products, which include recombinant protein expression and purification. The duties include preparing buffer solutions and cell culture media, performing bacterial cultures, affinity purifying recombinant proteins, and performing DNA isolation according to standard operating procedures. He or She may have additional responsibilities including transferring the products to other groups for testing, preparing product/project-related documentation, and maintaining the inventory and record for recombinant protein products. | 09/05/2024 |
| 2582 | Revvity San Diego, CA Research Associate I - Antibody Applications (IHC, ICC, Flow Cytometry, WB) Bachelor’s or Master's Degree in Biology, Immunology, Biochemistry, Neuroscience or other related fields Exp: 1 year |
Biolegend’s Research Associate position conducts antibody characterization and supports product development in Immunology, Oncology, Stem Cells and Neuroscience, encompassing various antibody applications including SDS-Page and Western blot, Immunoprecipitation, ELISA, flow cytometry, immunocytochemistry, immunohistochemistry, etc. This position will be responsible for effectively collecting, communicating and summarizing experimental data. | 09/05/2024 |
| 2583 | Revvity San Diego, CA Research Associate I - Tissue Culture Bachelor of Science in biology or a related field Exp: 1+ years |
This position is responsible for developing cutting-edge recombinant protein/antibody products in the Molecular & Cellular Biology (MCBio) group. The research associate will be involved in developing new lines of recombinant protein/antibody products by supporting projects and team members. The duties include preparing buffer solutions and cell culture media, maintaining cells cultures, and purifying recombinant proteins/antibodies according to standard operating procedures. Other job responsibilities include transferring the products to other groups for testing, preparing product/project-related documentation, and maintaining the inventory and record for recombinant protein/antibody products. This role will also support R&D projects to increase efficiencies or develop new technologies for the group. | 09/05/2024 |
| 2584 | Revvity Lafayette, CO Scientist I Bachelor's degree in chemistry or a life sciences discipline Exp: 1-3 years |
Revvity has a rewarding and exciting opportunity for an enthusiastic Scientist 1 for our Custom Synthetic Manufacturing laboratory. The Scientist 1 position will perform primary tasks in an ISO 9001:2015 laboratory in Lafayette, CO, Key responsibilities for this position include a wide array of duties related to the manufacturing of RNA and DNA oligonucleotides. This includes custom synthesis, cleaving, quality and quantity determination of product for customers. The position will require the ability to learn and to troubleshoot various aspects of manufacturing chemistry in multiple laboratories. | 09/05/2024 |
| 2585 | Societal CDMO Gainesville, GA QC Analyst I Bachelor’s Degree in chemistry or related scientific discipline Exp: 1 year |
We are looking for a QC Chemist I. In this role, you perform QC analytical activities in a highly regulated GMP environment. Activities include but are not limited to analytical method development, method validation, raw material testing, in process, release, and stability testing. Draft protocols, reports and procedures for analytical test methods, validation, and stability study. Hands on experience but not limited to HPLC, GC-FID, LC-MS, dissolution, FTIR, UV spectrophotometry, TOC, analytical balance, and Karl Fisher equipment. | 09/05/2024 |
| 2586 | Isolere Bio Research Triangle Park, NC Engineer/Scientist I - Reagent Development Bachelor’s Degree in engineering or other relevant scientific discipline Exp: 1-3 years |
As an Engineer/ Scientist I in the Reagent Development team, you will support the development and scaling of IsoTag™ reagents by producing smaller scale lots for testing and further development. The Development team is responsible for scaling production processes from the R&D team and optimizing them for use in manufacturing. This role will also assist with the initial production of IsoTag™ reagents with the manufacturing team, assisting with qualifying and validating the reagent production processes. | 09/05/2024 |
| 2587 | Hologic San Diego, CA Research Associate 2 B.A. /B.S. Molecular Biology, Chemistry, Biochemistry or related field Exp: 1-3 years |
Hologic is seeking a Research Associate 2 responsible for designing and performing experiments to support assay development including: feasibility, design transfer, assay integration and assay verification. Candidate accountable for effectively communicating results, collaborating with team members, and troubleshooting. | 09/05/2024 |
| 2588 | Hologic Newark, DE Senior EMC/RF Compliance Engineer Master’s Degree Exp: 1-3 years |
The Senior Compliance Engineer will be responsible for defining and executing product compliance strategies, policies, and processes to ensure that the company’s products meet regulatory standards and compliance certifications are obtained and maintained for global markets (e.g., ISO, FCC, UL, IEEE). The Senior Compliance Engineer will work closely with regulatory agencies and is the technical subject matter expert for regulatory compliance. Apply today! | 09/05/2024 |
| 2589 | Hologic Newark, DE Senior Electrical Engineer Masters Degree Exp: 1-3 years |
Hologic is seeking Senior Electrical Engineer to lead the design of a complete and complex framework, system, and products. You will be expected to design, develop, modify and evaluate components and processes used in the generation, manipulation, transmission and storage of electricity. You will be expected to determine design approaches and parameters. | 09/05/2024 |
| 2590 | Hologic San Diego, CA Mechanical Design Engineer 1 BS in Mechanical Engineering Exp: 0-3 years |
In this role, you will be part of a multidisciplinary engineering team developing and sustaining medical diagnostic instruments including mechanical design and manufacturing. You will be expected to bring hands-on experience and knowledge in mechanical design and manufacturing while utilizing sound engineering judgement and first principals. You will be expected to design, prototype, and test various electromechanical concepts to provide rapid feedback and direction to the broader development team to drive fast and decisive decisions. Interfacing with outside vendors on rapid prototyping, machining, molding, and advanced manufacturing processes is required. This is a fast-paced position that demands the ability to quickly adapt to evolving changes within the instrument, assay, and user needs. You will be working across functional groups such as Systems Engineering, Assay Development, Manufacturing, and Process Transfer. Clear communication, the ability to collaborate with others, and being a self-starter are a must. | 09/05/2024 |
| 2591 | SonoThera South SF, CA Temporary Research Associate, Protein/Metabolome Analytics Bachelor's degree in the biological sciences Exp: 0-3 years |
The Gene Therapy group at SonoThera is seeking to hire an entry-level Research Associate to become an integral part of the gene therapy drug development effort. We seek candidates who think critically and have the desire and ability to learn new techniques. This position requires adaptability and an ability to perform at a high level in a fast-paced environment. A qualified candidate will have technical experience in preparation of samples for protein and metabolite analyses. In this position, you will play an integral role in characterizing gene therapy vector delivery efficiency in diverse preclinical models. You will develop and optimize protocols for multiple assays, including but not limited to, immunoassays (ex. ELISA/MSD, Western blot, etc.), colorimetric and enzymatic assays for various efficacy and safety endpoints. | 09/05/2024 |
| 2592 | SouthernBiotech Birmingham, AL Quality Control Technician Bachelor’s Degree in Science Exp: 1 year |
We are currently seeking a Quality Control Technician for testing products, such as antibodies and proteins, following SOP’s and ISO requirements. | 09/05/2024 |
| 2593 | Sovereign Pharmaceuticals Fort Worth, TX QC Chemist II BA/BS Chemistry Exp: 1 year |
The primary function of a QC Chemist II is to perform to a high level in qualitative and quantitative chemical and physical analysis in support of two of the following areas: Analysis of raw materials and packaging components, Analysis of in-process and finished drug products (including stability) of primarily high-volume products, Analysis of high potency products | 09/05/2024 |
| 2594 | Spanios Houston, TX Project Bioengineer I MS in Bioengineering Exp: 1 year |
This job is suitable for an individual with meticulous skills for compilation, analysis, presentations, and communication of data from multiple projects with the CSO and COO for the purpose of documentation and communication with the clients. Someone who can co-ordinate Research Associates working on different projects to receive data for further distribution. This position will offer a unique and rewarding translational research experience in a dynamic and highly productive environment. | 09/05/2024 |
| 2595 | Spanios Houston, TX Research Associate I Bachelors degree Exp: 1 year |
This job is suitable for a responsible, skilled individual someone who can handle multiple projects and can follow instructions to complete assignments under minimal supervision. This position will offer a unique and rewarding translational research experience in a dynamic and highly productive environment. As a Research Associate you will provide responsible assistance for establishment and propagation of organoid cultures. | 09/05/2024 |
| 2596 | Spark Therapeutics Philadelphia, PA PD Downstream Scientist MS in chemical engineering, biochemistry, chemistry, biophysics, or related area Exp: 0-4 years |
The downstream process development (DSPD) team is seeking a highly motivated and innovative scientist to join our downstream purification technology development team. The successful candidate should have solid technical training in scientific and/or engineering discipline, preferably having biopharmaceutical industry experience. She/he will participate in multiple downstream process development projects for early or late phase program, with a focus on developing platform technology, continued process and product understanding and bringing innovation in adeno-associated virus (AAV) vector purification and characterization. | 09/05/2024 |
| 2597 | Spark Therapeutics Philadelphia, PA Research Associate - Upstream Process Development B.S. in chemical engineering, chemistry, biochemistry, or biology/molecular biology or related area Exp: 0-2 years |
The Upstream Process Development Research Associate is involved in the execution of recombinant adeno-associated viral vector (rAAV) production processes. The Research Associate executes experiments, aggregates and reviews experimental data, verifies data in technical reports and works under supervision of senior technical leads. | 09/05/2024 |
| 2598 | SparX Mount Prospect, IL Research Associate, in vitro Pharmacology Master’s degree in cell biology, oncology, immunology or related field Exp: 1 year |
SparX is looking for a highly motivated, interactive and creative Research Scientist with a strong cell biology background to join the pharmacology team. The primary responsibilities of the Research Associate will be to develop and perform in vitro cellular and/or biochemical assays for antibody drug candidates screening, biological function evaluation in immuno-oncology and oncology drug discovery program. | 09/05/2024 |
| 2599 | WuXi Advanced Therapies Philadelphia, PA Quality Control Environmental Monitoring Associate I Bachelor’s degree with a major in Biology, Microbiology, or related Life Science Exp: 0-3 years |
The Quality Control Environmental Monitoring Associate I is responsible for performing sampling and testing in support of manufacturing and validation activities, under the direction of a Supervisor or higher. Works in a team environment with various laboratory staff. | 09/05/2024 |
| 2600 | HD Biosciences San Diego, CA Research Associate I Bachelors in Life Sciences or related field preferred Exp: 0-1 years |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its Discovery Biomarkers team. We’re seeking a highly motivated Research Associate I to support our in vitro/ex vivo immunology team for various projects. | 09/05/2024 |
| 2601 | WuXi Advanced Therapies Philadelphia, PA Manufacturing Associate I - 1st Shift Bachelor’s (science preferred) degree Exp: 0-2 years |
The Manufacturing Associate I is responsible for manufacture of Master and Working Cell Banks and performing activities within production facilities to support manufacture of Cell & Gene Therapy products, and final product fills according to current Good Manufacturing Practices (cGMPs). | 09/05/2024 |
| 2602 | HD Biosciences San Diego, CA Research Associate II (Temp/Contingent) Master degree in Molecular and Cell Biology or Bachelor degree Exp: 1-2 years |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly skilled and motivated Research Associate II to support our in vivo pharmacology team for various projects. | 09/05/2024 |
| 2603 | Staar Surgical Monrovia, CA Quality Engineer I Bachelor’s degree, preferably in science or engineering Exp: 1 year |
Support site production, operations, and quality and R&D teams by addressing emergent issues that might arise due to the operation processes. Serve as the quality representative during any product or process investigation. Lead investigations including root cause analysis and health risk assessment of the identified product or process nonconformities. Prepare and execute validations, technical studies, test method validations and other studies / reports as required. This includes preparation of protocols, establishment of test methodology and acceptance criteria, training personnel, execution, data analysis, investigation, and writing final reports. Support project teams on non-conformance investigations regarding component failures, finished goods failures, and product returns. This includes but is not limited to performing risk analysis, determining root cause and recommending corrective action and SCRs. | 09/05/2024 |
| 2604 | Stability Biologics San Antonio, TX QA Specialist BS degree in a scientific discipline (Chemistry, Biology, Physics, Bio-Medical Engineering/Chemical Engineering, etc.) Exp: 1 year |
The Quality Assurance Specialist (QAS) will be a member of the Stability Biologics Quality Dept. to perform quality record reviews, batch release, record retention, data entry, auditing, investigations and document control activities. The QAS will be responsible for quality assurance metrics, CAPA/NCMR and maintaining all quality records/batch records in a secure and controlled manner. The QA Specialist will also be responsible for ensuring all policies and procedures are in compliance with appropriate FDA, AATB, states, and Stability Biologics standard operating procedure. | 09/05/2024 |
| 2605 | Stellartech Research Corporation Milpitas, CA Associate Quality Engineer Bachelor’s degree or equivalent Exp: Entry level |
Perform quality engineering development activities for new product designs by assisting Engineering in the preparation of design and development plans, Design History File documentation, and Design History File preparation. Review and approve Device Master Record documentation for new product design and maintenance, including bills of material, assembly procedures, manufacturing operations, assembly diagrams, test procedures, component specifications, labeling, and operator’s manuals. Perform ongoing quality engineering activities on current products to improve product designs and/or manufacturing processes including participation in NCM, Complaint, and CAPA investigations and actions as necessary. Assist in process validation activities for new and current products. Assist in maintenance and improvement of the Quality System with guidance of QA Management, including internal audits, external audits, and quality improvement activities. Assist Engineering in the preparation and execution of verification and validation protocols and verification and validation test reports for new products and changes to current products. | 09/05/2024 |
| 2606 | Stereotaxis St. Louis, MO System Test Engineer Bachelor's degree in Electrical Engineering, Mechanical Engineering, Biomedical Engineering, or other related degree highly preferred Exp: 1-2 years |
The System Test Engineer will be working within the system test team and collaborating with a cross-functional team to test and commercialize Stereotaxis products. The role will be working alongside various engineering disciplines and participating in development of test cases used for design verification and design validation activities in an ever-changing environment. | 09/05/2024 |
| 2607 | STERIS Coon Rapids, MN Scientist I - Validations B.S. degree in a technical discipline (engineering, physics, biology, chemistry, etc.) Exp: Entry level |
Responsible for the activities related to the coordination of validation of sterilization processes across STERIS operating facilities. This will NOT be a laboratory-based position. Activities include calibration of data collection systems, such as maintaining dosimeters and dosimetry equipment, measurement of dosimeters for report generation; operation, and data collection related to portable temperature/humidity sensors; coordinating with external laboratories for equipment calibrations and maintenance; coordinating with Customers for test sample processing and requalification studies; coordination and proper handling of product samples for transfer to outside laboratories for testing; and other routine tasks as directed by the immediate supervisor or manager. | 09/05/2024 |
| 2608 | Radionetics Oncology San Diego, CA Research Associate I Bachelor’s degree in biology or a related scientific discipline. Exp: 1 year |
The Research Associate I (RA) is a highly motivated lab bench scientist that contributes to multiple active research programs and is a valuable member of a collaborative team. The RA maintains cell lines, validates antibodies for flow cytometry, and performs flow cytometry analysis to determine target protein copy number at the cell surface to support cell line selection for in vivo model development for lead compound identification. The RA analyzes and interprets flow cytometry data and presents results in in vitro team meetings. The RA adopts and learns new processes quickly to be able to operate independently at the bench. | 08/30/2024 |
| 2609 | RayzeBio Indianapolis, IN Production Operator, Isotope Production Bachelor’s Degree in a STEM field Exp: 1-4 years |
The Operator – Isotope Production will be an integral part of bringing RayzeBio’s innovative drug products to patients in need. As Operator – Isotope Production, you will be instrumental in implementing a novel isotope production program that will manufacture the clinical and commercial scale radioisotopes for RayzeBio’s drug products. This individual will be part of a team responsible for producing RayzeBio’s radioisotopes under Good Manufacturing Practices (GMP). Additionally, you will be the front line in ensuring compliance with radiation safety requirements on the production floor. The Operator – Isotope Production will report directly to the operations leader of Isotope Production. Operator level will be evaluated with experience and qualifications. | 08/30/2024 |
| 2610 | RayzeBio Indianapolis, IN Radiopharmaceuticals Production Operator II Bachelor’s Degree in a STEM field Exp: 1-4 years |
The Radiopharmaceuticals Production Operator will be an integral part of bringing RayzeBio’s innovative drug products to patients in need. As the Production Operator, you will play an active role in daily operations, striving to ensure each batch is right the first time and that the production area is kept in order at our manufacturing site in Indianapolis IN. You will be responsible for the production of RayzeBio drug products, strictly complying with good manufacturing practice and aseptic requirements. Additionally, you will be the front line in ensuring compliance with radiation safety requirements on the production floor. As RayzeBio expands the production site and its portfolio of new products, the Production Operator will support validation work for future company initiatives, and support management with internal projects and new hire training. The Radiopharmaceuticals Production Operator will report directly to the Production Manager. Operator level will be evaluated with experience and qualifications. | 08/30/2024 |
| 2611 | RayzeBio San Diego, CA Associate Scientist I/II, Chemistry BS or MS in Chemistry or related field with strong understanding of organic and analytical chemistry Exp: BS 2-5 years’ or MS 0-4 years’ |
The Associate Scientist will work as part of a team of scientists to synthesize and design analogs to optimize potency, pharmacokinetics, and in vivo efficacy of potential drug candidates. | 08/30/2024 |
| 2612 | Reckitt Wanamingo, MN Compliance Assurance Lead Bachelor’s Degree in technical discipline (science/ engineering/ food processing, etc) Exp: 0-2+ years |
Our supply chain is the backbone of our business. It's how we get our trusted products to people all over the world, safely and efficiently. And it's our talented and passionate teams that make this happen. If you're looking for a career in supply chain, there's no better place to be than Reckitt. We offer a variety of exciting opportunities in all areas of the supply chain, from planning and procurement to manufacturing and logistics. You could join our Global Supply Planning team to develop and implement our global supply strategy, or work with our Procurement Centre of Excellence team to negotiate and manage our supplier relationships. Our Manufacturing Excellence team help us improve the efficiency, quality and safety of our manufacturing operations, and our Logistics Excellence team develop new and innovative ways to distribute our products to customers. | 08/30/2024 |
| 2613 | Reckitt St. Louis, MO Project Engineer B.S. Engineering Discipline (Electrical, Chemical, Mechanical) Exp: 1-3 years |
Seeking an engineering leader eager to make an impact! As the Engineering Manager within one of our agile-factory teams, you'll be the spark that drives project efficiency and innovation. Be at the forefront of managing an exceptional team, turning strategic plans into reality and leading the charge in our manufacturing success. Standard engineering is not what we do – we're about pioneering. If you're passionate about leading change and enhancing how we operate, you could be the perfect fit for us. | 08/30/2024 |
| 2614 | Reckitt St. Peters, MO Project Engineer B.S. Engineering Discipline (Electrical, Chemical, Mechanical) Exp: 1-3 years |
Seeking an engineering leader eager to make an impact! As the Engineering Manager within one of our agile-factory teams, you'll be the spark that drives project efficiency and innovation. Be at the forefront of managing an exceptional team, turning strategic plans into reality and leading the charge in our manufacturing success. Standard engineering is not what we do – we're about pioneering. If you're passionate about leading change and enhancing how we operate, you could be the perfect fit for us. | 08/30/2024 |
| 2615 | RefleXion Medical Hayward, CA Installation Engineer - Hybrid Bachelor’s of Science (BS) degree in electrical, mechanical or similar engineering field Exp: Recent College Grads encouraged to apply! |
The Installation Engineer will perform installations of RefleXion’s breakthrough radiation therapy technology at customer sites. The Installation Engineer must be proficient with hands-on equipment assembly and testing. The Installation Engineer will interact with various customer stakeholders and RefleXion resources with the highest level of professionalism and competence. | 08/30/2024 |
| 2616 | Regel Therapeutics Cambridge, MA Research Associate, Molecular Biology BA/BS or MS in biology or related field Exp: 1-3 years |
Regel Therapeutics is a gene modulation therapy company focused on improving the life of patients suffering from disorders resulting from alteration of gene expression. Our proven T3 (Targeted Therapeutic Technology) platform combines AAV delivery with two proprietary technologies for efficient and specific restoration of gene expression exclusively in the cells affected by the pathology. We are a seed-stage startup based in Cambridge, MA and Berkeley, CA and we are looking for a talented Research Associate to join our R&D team to help develop our preclinical programs. Perform molecular analysis of nucleic acid and protein levels in animal tissue to support preclinical development efforts. Maintain organized and detailed documentation of activities in an electronic notebook. Communicate research findings to the R&D team | 08/30/2024 |
| 2617 | Regeneron East Greenbush, NY Associate Process Characterization & Technology Scientist B.S in Biology, Chemistry, Biochemistry or related life sciences field. Exp: 0-2 years |
Regeneron is currently looking for a Process Characterization & Technology Scientist to join the process characterization and controls cell culture team within the Process Sciences department. This is a lab based position with a 1st shift, Wednesday- Saturday, 6am-4:30pm schedule. The Process Characterization and Technology Scientist is responsible for characterizing the cell culture manufacturing operations through laboratory-scale experiments, drawing conclusions via statistical analysis, and authoring technical summary reports. | 08/30/2024 |
| 2618 | Regeneron Tarrytown, NY Laboratory Assistant II, Analytical Chemistry BS Exp: 0-2+ years |
The Laboratory Assistant II will support the staff members in the Analytical Chemistry group through general administrative duties as well as laboratory and equipment upkeep. | 08/30/2024 |
| 2619 | Regeneron Tarrytown, NY Associate Scientist - DNA Core BS/MS Exp: 0-3 years |
We are seeking a collaborative and motivated Associate Scientist to join the DNA Core. Our group provides Regeneron laboratories with services vital for conducting scientific research, including plasmid preparation and purification. | 08/30/2024 |
| 2620 | Regeneron East Greenbush, NY Associate Process Characterization & Technology Scientist B.S in Biology, Chemistry, Biochemistry or related life sciences field. Exp: 0-2 years |
Regeneron is currently looking for a Process Characterization & Technology Scientist to join the process characterization and controls cell culture team within the Process Sciences department. This is a lab based position with a 1st shift, Wednesday- Saturday, 6am-4:30pm schedule. The Process Characterization and Technology Scientist is responsible for characterizing the cell culture manufacturing operations through laboratory-scale experiments, drawing conclusions via statistical analysis, and authoring technical summary reports. | 08/30/2024 |
| 2621 | Regeneron Rensselaer, NY QC Analyst - Sample Management BS/BA in Life Sciences, or related field Exp: 12-18+ months |
Regeneron is currently looking to fill a QC Analyst position in our QC Sample Management department with a 3rd shift schedule, Saturday-Wednesday, 10pm-8:30am. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Quality Control’s role is to ensure product quality and patient safety. Our QC Sample Management department acts as the gatekeepers of QC, accessioning and triaging samples as they are submitted for testing; the QC Analyst position performs a variety of sample receipt functions as well as routine sample inventory and disposal. | 08/30/2024 |
| 2622 | Regeneron Tarrytown, NY Associate Scientist BS degree or MS degree in a scientific field Exp: 0-3+ years |
Regeneron's Clinical Bioanalysis group, located in Tarrytown NY, is seeking an Associate Scientist. Train on bioanalytical methods (manual, hybrid, and automated) and completes methods to perform bioanalysis for clinical studies under supervision. Analyze multiple plates within the same day and may perform multiple assays within the same day. Interpret data to assess plate acceptance criteria and adjust sample dilutions accordingly. Complete vital operations in LIMS (requesting samples, building analysis plates, tracking sample movement, tracking pending analysis and performing data entry). Uses the ELN for data documentation purposes. Prepares and qualifies reagents, and re-orders laboratory supplies and reagents, as needed. Ensures compliance, as appropriate, for all laboratory work and documentation in accordance with working practices, company SOPs, bioanalytical method procedures (BMPs), and regulations. | 08/30/2024 |
| 2623 | Regeneron Rensselaer, NY Associate Biotech Production Specialists BS/BA in Life Sciences or related field Exp: Entry Level, New Grad |
Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Our Associate Biotech Production Specialists are on the front line, producing our life changing products and have a passion for assisting those in need by using biotechnology. They perform all tasks necessary for the manufacturing operations of both clinical and commercial manufacturing programs. | 08/30/2024 |
| 2624 | Renaissance Lakewood, NJ Compounder II, 3rd shift Bachelor’s Degree Exp: 0 years |
Primary Responsibility for execution of bulk product batch processing, inclusive of all process related and administrative activities, as well as Equipment Preparation activities as declared in Compounder 1. | 08/30/2024 |
| 2625 | Renaissance Lakewood, NJ Compounder II, 3rd shift Bachelor’s Degree Exp: 0 years |
Primary Responsibility for execution of bulk product batch processing, inclusive of all process related and administrative activities, as well as Equipment Preparation activities as declared in Compounder 1. | 08/30/2024 |
| 2626 | Renaissance Lakewood, NJ Compounder II, 2nd shift Bachelor’s Degree Exp: 0 years |
Primary Responsibility for execution of bulk product batch processing, inclusive of all process related and administrative activities, as well as Equipment Preparation activities as declared in Compounder 1. | 08/30/2024 |
| 2627 | Renaissance Lakewood, NJ Compounder II, 2nd shift Bachelor’s Degree Exp: 0 years |
Primary Responsibility for execution of bulk product batch processing, inclusive of all process related and administrative activities, as well as Equipment Preparation activities as declared in Compounder 1. | 08/30/2024 |
| 2628 | Rigel Pharmaceuticals South SF, CA Clinical Trial Assistant Bachelor’s degree in science related field required. Exp: 1-2 years |
This opportunity will support the Clinical Operations team in a fast paced, busy hematology/oncology pharmaceutical development department. As a Clinical Trial Assistant (CTA), you will assist the clinical research teams in clinical trial conduct, oversight, and logistics by providing administration and project tracking support. | 08/30/2024 |
| 2629 | RION Rochester, MN Research Associate Bachelor’s or Master’s degree with focus in Biological Sciences Exp: 1+ years |
The Research Associate will contribute to ongoing scientific projects within the Research and Development laboratory focused on Rion’s exosome technology. As such, the candidate will possess the technical skills required to conduct experiments and assays in a wet lab environment involving techniques such as mammalian cell culture, flow cytometry, ELISA, RT-qPCR, and colorimetric/fluorometric-based assays. The Research Associate will be responsible for the execution of experiments, as well as data interpretation and final reporting. The position affords the opportunity to serve as a key member of Rion’s scientific team and contribute to the advancement of exosome therapeutics. The Research Associate will work closely with the Research and Development Scientists and support the efforts of Quality Control and Process Development. As such, the successful candidate will work in an upbeat, highly collaborative and dynamic environment. Additional responsibilities associated with this position will involve assisting in day-to-day laboratory operations such as inventory management, procurement, and general laboratory and equipment maintenance. | 08/30/2024 |
| 2630 | Sai Life Sciences Watertown, MA Senior Research Associate - Biology Master's degree in Biology Exp: 1+ years |
As the Senior Research Associate in Biology, you will play a crucial role in conducting groundbreaking research, contributing to our mission of advancing scientific knowledge and addressing pressing biological challenges. Working closely with our team of scientists, you will be involved in various aspects of experimental design, data collection, analysis, and interpretation. This position offers an exciting opportunity to be at the forefront of scientific discovery and make a meaningful impact in the field of biology. You’ll have the opportunity to develop your skills to work independently and advance your knowledge-base on assay development and optimization. | 08/30/2024 |
| 2631 | Sai Life Sciences Watertown, MA Research Associate - Biology Bachelor's or Master's degree in Biology Exp: 1+ years |
As the Research Associate in Biology, you will play a crucial role in conducting groundbreaking research, contributing to our mission of advancing scientific knowledge and addressing pressing biological challenges. Working closely with our team of scientists, you will be involved in various aspects of experimental design, data collection, analysis, and interpretation. This position offers an exciting opportunity to be at the forefront of scientific discovery and make a meaningful impact in the field of biology. | 08/30/2024 |
| 2632 | Sanofi Swiftwater, PA Production Technician - Vaccine Bachelors Exp: 0+ years |
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Your job, as a Production Technician - Vaccine within our Packaging Team, will have the potential to transform the practice of medicine, turning the impossible into possible for millions of people. | 08/30/2024 |
| 2633 | Sanofi Chattanooga, TN Quality Control Chemist Lab I (2nd shift) Bachelor’s degree in chemistry or related field Exp: 0-3 years |
The Quality Control Lab Chemist will perform routine testing to support production and release of product in compliance with established specifications. Perform testing of ingredients as required to support production requirements. Assure that testing is properly documented, and that the ingredient is dispositioned in accordance with the results of the test and the appropriate standard operating procedures.Perform routine laboratory testing for bulk and finished product to support production or shipping requirements. Assure that testing is properly documented and that the bulk or finished product is dispositioned in accordance with the results of the test and the appropriate standard operating procedures. Perform stability testing in support of the room temperature stability program. Assure that stability testing is completed in a timely manner and within the designated time frame. Complete stability testing documentation as appropriate. Knowledge of and ability to use lab instruments including but not limited to: UV-VIS, HPLC, GC, ICP, AA, and FTIR. | 08/30/2024 |
| 2634 | Sanofi Swiftwater, PA Production Technician - Vaccine Bachelors Exp: 0+ years |
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Your job, as a Production Technician - Vaccine within our Packaging Team, will have the potential to transform the practice of medicine, turning the impossible into possible for millions of people. | 08/30/2024 |
| 2635 | Sanofi Chattanooga, TN Quality Control Lab Chemist I Bachelor’s degree in chemistry or related field Exp: 1-3 years |
The Quality Control Lab Chemist will perform routine testing to support production and release of product in compliance with established specifications. Perform testing of ingredients as required to support production requirements. Assure that testing is properly documented, and that the ingredient is dispositioned in accordance with the results of the test and the appropriate standard operating procedures.Perform routine laboratory testing for bulk and finished product to support production or shipping requirements. Assure that testing is properly documented and that the bulk or finished product is dispositioned in accordance with the results of the test and the appropriate standard operating procedures. Perform stability testing in support of the room temperature stability program. Assure that stability testing is completed in a timely manner and within the designated time frame. Complete stability testing documentation as appropriate. Knowledge of and ability to use lab instruments including but not limited to: UV-VIS, HPLC, GC, ICP, AA, and FTIR. | 08/30/2024 |
| 2636 | Sanofi Waltham, MA Senior Associate Scientist MSc or BSc Exp: MSc: +1 year; BSc: +1-3 years |
The primary responsibilities of the Senior Associate Scientist, Virology will be to support covid vaccine projects by generating and characterizing SARS-CoV-2 pseudovirus materials and maintaining the production lab. Individual will support optimization of pseudovirus capabilities and assay development as needed for the project and departments. The successful candidate will be required to generate, analyse and document data and to communicate their results internally. The candidate will be required to liaise effectively with the team. | 08/30/2024 |
| 2637 | Santa Cruz Biotechnology Paso Robles, CA Research Assistant Bachelor of Science in Biology, Microbiology, Cellular Biology, Biochemistry, or similar field of study. Exp: Entry Level |
Santa Cruz Biotechnology has an immediate opening for an entry level Research Assistant at our Paso Robles, CA campus. This is a full time position with career advancement opportunities within the company. Ability to perform standard analytical and preparative procedures required for the development and analysis of monoclonal antibodies. Ability to characterize antibodies by designing and optimizing experiments, interpreting data, and selecting the best possible products to develop. Capacity to utilize established, routine procedures and follows instructions from supervisor. Strong scientific background and business communication skills. | 08/30/2024 |
| 2638 | Santa Cruz Biotechnology Santa Cruz, CA Research Assistant Bachelor of Science in Biology, Microbiology, Cellular Biology, Biochemistry, or similar field of study. Exp: Entry Level |
Santa Cruz Biotechnology has an immediate opening for an entry level Research Assistant at our Paso Robles, CA campus. This is a full time position with career advancement opportunities within the company. Ability to perform standard analytical and preparative procedures required for the development and analysis of monoclonal antibodies. Ability to characterize antibodies by designing and optimizing experiments, interpreting data, and selecting the best possible products to develop. Capacity to utilize established, routine procedures and follows instructions from supervisor. Strong scientific background and business communication skills. | 08/30/2024 |
| 2639 | Sapere Bio Research Triangle Park, NC General Supervisor, CLIA Laboratory Master's or Bachelor’s degree in clinical laboratory science, medical technology or chemical, physical, or biological science Exp: 1 year |
The General Supervisor provides day-to-day supervision of testing personnel. The General Supervisor is responsible for the proper performance of all laboratory procedures and reporting of test results.Perform accurate and timely laboratory testing according to SOPs within the allowable timeframe. Demonstrate the ability to use good judgement and independent thinking in data analysis and interpretation of patient results. Maintain all Quality Management System on instrument maintenance programs, i.e. preventative maintenance, cleanliness, and maintains records of service in compliance with CLIA. Review testing issues with the Technical Supervisor to get direction for troubleshooting and next steps. Ensure that all remedial actions are taken whenever test systems deviate from the laboratory's established performance specification. Provide leadership and direct a team of technologists through positive communication and support. Train new personnel with regard to technical and operational procedures. Ensure all laboratory members are proficient in assay processing, including biannual (first year) and subsequent annual competency training. Work with the lab team to monitor and maintain inventory of supplies and place orders of materials. Participate in managing all governmental and regulatory audits. Manage and monitor Quality Control (QC), Quality Assurance (QA), Safety and Inspection practices to assure compliance with CLIA regulations. | 08/30/2024 |
| 2640 | Saptalis Hauppauge, NY Analytical Scientist B.S/M.S/Ph.D in Analytical Chemistry or related discipline Exp: 0-2 years |
Saptalis is looking to recruit Analytical Scientists to join the growing Analytical R&D group at our facility in Hauppauge, NY. Analytical Scientist is responsible for developing and validating analytical methods for analytes of interest in new drug products using UPLC, HPLC, GC and other analytical instruments. Execute all functions in accordance with current FDA regulations, ICH guide lines, USP methodologies, cGLPs and Saptalis SOPs. | 08/30/2024 |
| 2641 | Saptalis Hauppauge, NY Quality Control Scientist BS/MS Degree (chemistry or related field) Exp: 0-2 years |
Saptalis is looking to recruit QC Scientists to join the growing Quality group at our facility in Hauppauge, NY. QC Scientist is responsible for GMP testing of raw materials, in-process, finished product and stability samples for release. In addition, the responsibilities include maintaining laboratory equipment, assisting in investigations and coordinating external testing as needed. | 08/30/2024 |
| 2642 | Saptalis Hauppauge, NY Validation Associate Bachelor’s degree required, preferably in a science or engineering related field. Exp: 0-2 years |
Saptalis is looking to recruit a Validation Associate to join a growing Technical Operations group at our facility in Hauppauge, NY. Validation Associate is responsible for execution of qualification and validation programs for processing and testing equipment, computer systems, manufacturing processes and cleaning of manufacturing equipment as per FDA regulations and SOPs. | 08/30/2024 |
| 2643 | Scanogen Baltimore, MD Research Associate Bachelor in molecular biology, biotechnology, bioinformatics, biology, chemical engineering, bioengineering or related field Exp: 1 year |
To test and perform manual and automated molecular diagnostic assays. Perform and assist with bacterial and fungal cultures. Perform and assist with bacterial and fungal lysate preparation. Collect, prepare and process bacterial and fungal specimens. Collect and document research data. | 08/30/2024 |
| 2644 | Sciecure Pharma Monmouth Junction, NJ QC & ARD Chemist Bachelor’s degree from four-year college or university in any of the following disciplines: Chemistry, Biology, Microbiology, or related sciences Exp: 1 year |
The Analytical R&D laboratory supports, development and validation of methods analytical test methods, evaluation and testing of raw materials, and testing of non-commercial materials to support product development. All activities are performed in accordance with specifications, standard operating procedures, approved test methods and/or protocols, regulatory requirements | 08/30/2024 |
| 2645 | Sciecure Pharma Monmouth Junction, NJ Project Coordinator Bachelor’s degree in Life Science (Biology, Chemistry, Chemical Engineering, Etc.). Exp: 1-3 years |
Sciecure Pharma Inc. specializes in the research and development of pharmaceutical finished products from conception to commercial. Our growing company is seeking to hire a project coordinator who will be in charge of assisting in organizing our ongoing projects. This task involves monitoring project plans, schedules, organizing and participating in stakeholder meetings, and ensuring that project deadlines are met in a timely manner. To be successful as a project coordinator, you will need to be able to work on tight deadlines, be competent in using Microsoft Office applications such as Word and Excel, and have exceptional verbal, written, and presentation skills. A bachelor’s degree in life science is required for consideration. | 08/30/2024 |
| 2646 | ScienCell Research Laboratories Carlsbad, CA Associate Molecular Biologist Bachelor’s or Master’s degree in life science Exp: 1 year |
We are searching for an energetic and self-motivated candidate with a positive attitude and strong work ethic to fill our associate molecular biologist position in our R&D department. Responsibilities include, but are not limited to, working on cell-derived DNA, RNA, and proteins purification, gene expression analysis, performing PCR/RT-PCT/qPCR, SDS PAGE and UV spectrum for quantitation. Candidates should be familiar with electrophoresis, spectrophotometer, centrifugation and other basic laboratory techniques. General lab logistical skills such as record keeping, ordering supplies and ensuring general laboratory safety and cleanliness are also required. | 08/30/2024 |
| 2647 | Scientific Protein Laboratories Waunakee, WI Validation Associate B.S. in Chemistry, Biological Sciences or Engineering (Chemical, Electrical, Mechanical, Reliability) or related discipline Exp: No Exp |
Join our team at Scientific Protein Laboratories (SPL), a world leader in biosourced pharmaceuticals, located just outside of Madison, Wisconsin in Waunakee! SPL is an innovative biopharmaceutical leader with unique products and services supporting the pharmaceutical industry globally. For over 40 years, SPL specializes in the development and cGMP compliant manufacturing of Active Pharmaceutical Ingredients (APIs). SPL has an exciting opportunity to join the team as a Validation Specialist. This position is responsible for preparing and executing validation protocols for cGMP processes, production/laboratory equipment, cleaning procedures, and software in compliance with Q7. Writes final reports for executed validation protocols. Assists other Validation staff with their validation protocols. | 08/30/2024 |
| 2648 | Pfizer Bothell, WA Senior Associate Scientist- Conjugation M.S. degree Exp: 0-2 years |
The Protein and Bioanalytical Sciences (PBS) team is focused on creating and delivering novel research test articles for preclinical evaluation. As a Senior Associate Scientist, you will be at the center of our operations, and you’ll find that everything we do is in line with an unwavering commitment to quality. This position is responsible for preparing and analyzing novel Antibody Drug Conjugations (ADCs), developing new conjugation methods and analytical assays, and delivering critical reagents. This person will play a critical role in supporting Pfizer Oncology’s preclinical programs. Your strong foundation in quality scientific practices will help the team in meeting critical deadlines and exceeding milestones. You will be relied on as a technical contributor to make decisions that involve direct application of your knowledge. It is your hard work and focus that will make Pfizer ready to achieve new breakthroughs and help patients across the globe. | 08/21/2024 |
| 2649 | Pfizer Groton, CT Manufacturing Engineer Bachelors Level qualification in Chemical Engineering, Pharmaceutical Sciences, Materials Science or other Engineering discipline. Exp: For a newly qualified graduate or graduate with some initial industrial experience |
We are seeking a highly motivated person as Manufacturing Engineer in our Drug Product Manufacturing (DPM) facility. The successful candidate will learn and actively support a wide range of process development and manufacturing activities for clinical drug product supplies. Additionally, the colleague will contribute to the development of DPM technology capabilities (eg. Powder blending, granulation, tablet compression, encapsulation, film coating etc.) by supporting novel process development and process understanding studies. The successful candidate must demonstrate strong teamwork dynamics when interfacing with various groups (e.g., Operations, Quality, Tech Support) and a continuous improvement mindset. | 08/21/2024 |
| 2650 | Pfizer Pearl River, NY Lab Process Control Associate Bachelor’s degree in a relevant field (eg, science, business administration) Exp: 0-2 years |
The Lab Process Control Associate (P01) will report directly to CIHO’s Laboratory Process Control Lead and play a major role in ensuring operational excellence in CIHO’s compliant testing laboratories. The primary responsibility for this position is to assist CIHO’s Lab Process Control Lead to achieve success in aligning laboratory compliance across CIHO, which includes improving the lab process control document cycle times. The position will help the Laboratory Process Control Lead manage several Lab Process Control workflows including but is not limited to (i) Standard Operating Procedures (SOP) undergoing periodic review (authoring, review and approval); (ii) Laboratory Deviation Reports (LDR), Planned Deviation Notes (PDN), and Change Control Requests (CCR) from initiation through approval, required deliverables and any post approval commitments. Other routine duties will include (i) verification of documents associated with laboratory equipment qualification reports; (ii) standardization of common verbiage used in these CIHO documents; (iii) providing assistance in conducting LDR investigations. | 08/21/2024 |
| 2651 | Pfizer Pearl River, NY Associate Scientist - Clinical Immunology & High-Throughput Operations Bachelor's Degree in a relevant scientific discipline Exp: 0-2 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role to generate high-quality immunoassay data in a regulated Good Laboratory Practices (GLP) setting to support Pfizer’s vaccine programs according to Standard Operating Procedures. You will support the technology transfer and integration of new laboratory immunoassays into the cGLP space, support assay validation projects and monitor immunoassay lifecycle. In addition, you will also support throughput activities and provide testing support for clinical and non-clinical research programs. Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. | 08/21/2024 |
| 2652 | Pfizer Pearl River, NY Associate Scientist, High-Throughput Clinical Immunoassays and Diagnostics Bachelor's Degree in a relevant scientific discipline Exp: 0-3 Years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. The primary purpose of this position is to assist, develop and perform all aspects of preclinical and clinical functional assays, including, but not limited to serum bactericidal assay (SBA) using robotics or manual method, including all required documentation. Also, included activities are preparation of buffers, media, qualification of assay reagents and other duties assigned as necessary. All of the above includes practicing laboratory safety at all times. All work is to be done in a compliant manner according to relevant SOP guidelines and GLP and/or GMP guidelines, as required. In addition, you will also support throughput activities and provide testing support for clinical and non-clinical research programs. Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. | 08/21/2024 |
| 2653 | Pfizer Sanford, NC Technical Operations Engineer Bachelor's degree in any of the following disciplines: Chemistry, Biochemistry, Biotechnology, Chemical Engineering, and/or Biology Exp: 0+ years |
Working with Pfizer’s dynamic engineering team, you will play a critical role in supporting efforts to bring products from research to manufacturing. You will leverage your technical capabilities to understand the inherent problems of transfer of technology from the research stage to manufacturing, in cooperation with pilot-plant and production departments. You will conduct assessments and create procedures for materials and components used throughout the stages of production.As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative team environment for your colleagues. | 08/21/2024 |
| 2654 | Pfizer Pearl River, NY Associate Scientist - Sample Logistics and Solutions Bachelor of Science Degree Exp: 0-5 years |
The primary purpose of this job role is to function as a member of the Sample Logistics and Solutions (SLS) team within Pfizer Vaccine Research and Development (VRD). The incumbent will be responsible for receiving samples from global clinical/study trials according to approved protocols and processes. The individual will participate in all aspects of tracking and documenting the chain of custody of samples. The incumbent’s role will include sample receipt, documentation, storage, tracking, aliquoting, distribution to the testing labs, and sample disposal. The colleague will work in a team setting and will share roles and responsibilities as assigned by the team leader/manager. | 08/21/2024 |
| 2655 | Pharmaron Exton, PA Associate Scientist Bachelor of Science (Biology, Biochemistry, Pharmaceutical Life Sciences) Exp: 0-2 years |
Associate Scientist within our Cell Biology team is a pivotal role which requires a dynamic professional with strong experience in conducting various studies/assays while delivering exceptional quality with high attention-to-detail to ensure all clients expectations are met. | 08/21/2024 |
| 2656 | Pharpoint Research Durham, NC Quality Assurance Auditor Bachelor’s degree (B.A./B.S.) or equivalent in a scientific, computer, or related discipline. Exp: 1-2 years |
Performs project and non-project quality assurance duties at PharPoint Research. Responsible for carrying out quality initiatives at the company, including but not limited to SOPs and training, computer systems validation, and Quality Management System | 08/21/2024 |
| 2657 | Pierre Fabre Remote, Cell Therapy Operations Specialist, Associate I Bachelor's degree in science or health-related field required Exp: 1 year |
Pierre Fabre Pharmaceuticals is seeking a highly motivated, and well-organized Cell Therapy Operations Specialist (CTOS). This role will be the central point of contact for Health Care Professionals (HCP) from product availability inquiry through product receipt at the institutions. Additionally, this role will be responsible for selecting the product lot for the patient that meets the matching requirements, as well as answering and triage all inbound calls from HCPs. | 08/21/2024 |
| 2658 | Pierre Fabre Parsippany, NJ Cell Therapy Operations Specialist, Associate I Bachelor's degree in science or health-related field required Exp: 1 year |
Pierre Fabre Pharmaceuticals is seeking a highly motivated, and well-organized Cell Therapy Operations Specialist (CTOS). This role will be the central point of contact for Health Care Professionals (HCP) from product availability inquiry through product receipt at the institutions. Additionally, this role will be responsible for selecting the product lot for the patient that meets the matching requirements, as well as answering and triage all inbound calls from HCPs. | 08/21/2024 |
| 2659 | Poseida Therapeutics San Diego, CA TEMPORARY - Process Development Associate Bachelor’s or Master’s degree in Biological Sciences, Biomedical Engineering, Immunology or other related scientific field Exp: 0-2 years |
We are seeking an experienced and motivated Process Development Associate to join the late-stage Process Development & Manufacturing Sciences and Technology(MSAT) team at Poseida Therapeutics. The successful candidate will join a multidisciplinary team to support the allogeneic efforts for Poseida’s first allogeneic programs, as well as ongoing process changes for the clinical-stage autologous programs. This is a hands-on, laboratory-based role where the candidate will support the introduction and evaluation of new technologies into Poseida’s allogeneic processes and play a key role in process understanding. The ideal candidate will be a cell biologist/biological engineer with a proven track record of innovation, knowledge in process and analytical development, extensive cell culture experience, statistical process control methodologies, statistics, data analysis, and is excited to take on new challenges in a fast-paced and dynamic environment. Additionally, the Process Development Associate will be involved in donor characterization efforts, evaluating efficacy of CAR T cells in animal models, and may assist in the drafting of SOPs and production batch records of ongoing process changes. This is a contractor position reporting to the Senior Process Engineer, MSAT. This position is located at our headquarters in San Diego, CA. | 08/21/2024 |
| 2660 | Presage Biosciences Seattle, WA Histology Research Associate Bachelor’s degree (or equivalent experience) in Biology, Biochemistry, or related field Exp: 1-2 years |
We are seeking a highly motivated individual to join the histology team at Presage Biosciences, an innovative Seattle biotech start-up focused on improving cancer drug efficacy. Reporting to the histology manager you will perform routine histology tasks including specimen processing, embedding, microtomy, staining, and immunohistochemistry. This full-time role supports the development of a cutting-edge target validation and drug evaluation platform. | 08/21/2024 |
| 2661 | Profluent Berkeley, CA Associate Engineer, High Throughput Operations BS/MS in science or engineering discipline Exp: 0-2 years |
We are currently seeking a creative, passionate, and detail-oriented Associate Engineer to join the High Throughput Operations team. The focus of this role will be to develop and implement automated workflows for our in-house molecular cloning core, high throughput screening core, and NGS core. This candidate will work collaboratively with scientists, engineers, and bioinformaticians to develop a suite of assays for measuring gene editing activity and specificity. This is an excellent opportunity to shape the future of AI-driven protein design and to work cross-functionally with a diverse team of experts across machine learning, protein engineering, cell biology, and gene editing. | 08/21/2024 |
| 2662 | Promis Diagnostics Irvine, CA Laboratory Technician BS in Biology, Chemistry, or other medical-related sciences Exp: Entry level |
The Laboratory Assistant or Technician will follow the guidelines set by CLIA and the CA Business and Professional Code of Regulations (BPC: 1212 and 1269) for unlicensed laboratory personnel. Accessions and processes samples (pre-analytical) and prepares samples for testing. Assists CLSs with Preventative Maintenance procedures. Assists CLSs in Quality Control performance, troubleshooting, and in the preparation & storage of reagents. Assist in gathering Calibration and QC data for the CLS to approve before the release of any patient results. Records temperatures and humidity readings as well as other environments. Prepares, orders, and maintains reagents and supplies as required. Ensure that reagents are not used past their expiration date. Documents dating directly on reagents as required by CLIA. Assist QA Manager with QA activities, such as gathering monthly QC reports and assuring the proficiency testing binder is compiled correctly. Provides technical support to clients for our testing services. Will work in partnership with the scientific team in developing and validating new Epigenetics/Genetics tests, including cancer/tumor markers and other inherited disease-related genetic tests. Will collaborate with the scientific and testing personnel team to develop and validate new Molecular Infectious Disease Diagnostic tests for patient care using Real-Time PCR technology. Performs high-complexity laboratory testing in molecular diagnostics, including pharmacogenetics, personal diagnostics, infectious disease, tumor markers, and other molecular testing. | 08/21/2024 |
| 2663 | ProPharma Raleigh, NC Clinical Research Associate (Rare Disease) Bachelor's degree Exp: 0-3 years |
The Clinical Research Associate position is responsible for clinical monitoring for assigned protocols and investigational sites as well as ensuring that studies are conducted and documented in accordance with the study protocol, standard operating procedures, Good Clinical Practices (GCP) and other applicable regulatory requirements. | 08/21/2024 |
| 2664 | PSC Biotech Pomona, CA CQV Project Engineer I Bachelor's degree in relevant engineering discipline Exp: 1-3 years |
We are hiring an entry-level CQV Engineer. Candidates should have prior experience whether through internships or other related professional experience supporting C&Q and GDP/GMP technical documentation. | 08/21/2024 |
| 2665 | PSC Biotech Englewood, NJ Commissioning, Qualification, Validation Engineer I (CQV) Bachelor's degree in relevant engineering discipline Exp: 1-3 years |
We are hiring an experienced CQV Engineer I to support the commissioning, qualification, and validation for a range of equipment and systems within the pharmaceutical and/or medical device industry. | 08/21/2024 |
| 2666 | Psomagen Inc. Rockville, MD NGS Laboratory Technician/Scientist/Manager Bachelor’s degree in biology or relevant major are required Exp: 1 year |
Operate a computer-based laboratory system, record data, and perform laboratory tests. Perform experimental procedures using molecular biology techniques such as isolation of DNA/RNA, Quantification, NGS library construction, qPCR, operating sequencers, micro pipetting, and meticulous measuring. Prepare solution, reagents, and stains by adhering to standard laboratory formulas and procedures. Oversee equipment performance and maintenance schedules. May perform routine repair or replacement of standard parts. Monitor inventory levels, order materials, and supplies in accordance with the established policies and procedures. Troubleshoot problematic samples and results. Communicate effectively with clients and co-workers to improve the existing processes. Adapt to new services/technologies to enhance sales. Train and guide new team members and subordinates. Write and update protocols that meet the CLIA/CAP/ISO standard | 08/21/2024 |
| 2667 | PTC Therapeutics Bridgewater, NJ Research Associate II, Formulation Development Bachelor’s degree in material science, chemistry, chemical engineering or other related scientific discipline Exp: 1 year |
The Research Associate II, Formulation Development contributes to the drug discovery and drug product development process by developing and supporting formulations for preclinical and clinical evaluation and performing pre-formulation characterization studies to support drug product formulation development. This position works cross-functionally with internal departments and external resources on formulation support related issues. The Research Associate II, Formulation Development supports adherence to relevant sound scientific lab practices, regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate. | 08/21/2024 |
| 2668 | PTC Therapeutics Warren, NJ Clinical Operations Assistant Bachelor’s Degree Exp: 1 year |
The Clinical Operations Assistant provides administrative and project support to the Clinical Operations organization. This includes, but may not be limited to, proactively and independently identifying, coordinating, and monitoring the administrative aspects of the departments’ projects/programs and interacting with key stakeholders as necessary; identifying and implementing/supporting administrative systems, processes and procedures; and completing varied routine, ad-hoc and project-driven administrative tasks as assigned. The Clinical Operations Assistant supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate. | 08/21/2024 |
| 2669 | Q² Solutions Durham, NC Immunoassay Associate Scientist Bachelor’s degree in chemistry or a related field Exp: 1 year |
We are seeking an Immunoassay Associate Scientist to join Q² Solutions, IQVIA’s laboratory business in Durham, NC. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As an Immunoassay Associate Scientist, you will execute laboratory experiments with precision, contribute innovatively to scientific procedure design, and uphold the highest standards of Good Laboratory Practices (GLP) for our clients. You’ll not only set up and conduct experiments but also manage laboratory equipment, ensuring protocols are meticulously followed under the guidance of a dedicated lab services manager, researcher, or scientist. | 08/21/2024 |
| 2670 | Q² Solutions Durham, NC Associate Immunoassay Scientist Bachelor’s degree in chemistry or a related field Exp: 1 year |
We are seeking an Immunoassay Associate Scientist to join Q² Solutions, IQVIA’s laboratory business in Durham, NC. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As an Immunoassay Associate Scientist, you will execute laboratory experiments with precision, contribute innovatively to scientific procedure design, and uphold the highest standards of Good Laboratory Practices (GLP) for our clients. You’ll not only set up and conduct experiments but also manage laboratory equipment, ensuring protocols are meticulously followed under the guidance of a dedicated lab services manager, researcher, or scientist. | 08/21/2024 |
| 2671 | Q² Solutions Austin, TX Associate Scientist, Assay Development Bachelor's degree in relevant scientific discipline. Exp: 1 year |
We are seeking an Associate Scientist, Assay Developmentto join Q² Solutions, IQVIA’s laboratory business in Austin, TX. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As an Associate Scientist, you will be responsible for maintaining acceptable and accurate levels of raw and batched inventory in support of reagent manufacturing and production testing. | 08/21/2024 |
| 2672 | Q² Solutions Ithaca, NY Associate Scientist, Sample Preparation Bachelor’s Degree Exp: 1 year |
We are seeking an AssociateScientist, Sample Prepto join Q2 Solutions, IQVIA’s laboratory business atIthaca, NY. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As a Scientist, Sample Prep, you will be responsible for sample preparation duties, including troubleshooting routine experiments, preparing solutions and reagents, and driving process improvements. You will also play a key role in training junior level staff. | 08/21/2024 |
| 2673 | Q² Solutions Durham, NC Associate Scientist Bachelor’s Degree in a chemical, physical, biological, or clinical laboratory science, medical laboratory technology, or cytotechnology. Exp: 6 months |
We are seeking an Associate Scientist to join Q² Solutions, IQVIA’s laboratory business in Durham, NC. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. The Associate Scientist will be instrumental in conducting and documenting analytical procedures, ensuring compliance with SOPs and regulatory guidelines, and contributing to the advancement of our laboratory operations. | 08/21/2024 |
| 2674 | Q² Solutions Durham, NC QC Specialist Bachelor’s Degree in medical technology or equivalent. Exp: 1 year |
We are seeking a Quality Control Specialist to join Q2 Solutions, IQVIA’s laboratory business at Durham, NC. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As a Quality Control Specialist, you will be responsible for supporting lab quality control processes and improvements, ensuring accuracy and compliance with regulations and SOPs. | 08/21/2024 |
| 2675 | Q² Solutions Ithaca, NY Scientist, Lab Operations Bachelor’s Degree in applied/laboratory sciences with direct laboratory coursework. Exp: 0-2 years |
We are seeking aScientist Laboratory Operationsto join Q2 Solutions, IQVIA’s laboratory business atIthaca, NY. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Responsible for the accurate execution of laboratory experiments and contributing to the design of scientific procedures. This position aids in the development of scientific discovery and supports Good Laboratory Practices (GLP) for the customer. | 08/21/2024 |
| 2676 | QIAGEN Beverly, MA Finished Goods Formulation Technician II Bachelor’s of Science degree Exp: 1+ years |
The Finished Goods Formulation Technician II formulates buffers, diluents, and PCR master mixes for the Finished Goods team. This position is charged with adhering to the Quality System to execute consistent processes that result in repeatable product for on time delivery. | 08/21/2024 |
| 2677 | Quality Agents Rockville, MA Validation Engineer I BS in a technical discipline (Engineering, chemistry, microbiology, biology) Exp: 0-2 years |
Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. Our Validation specialists will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The validation specialist will evaluate the equipment/utility/system/procedures used in development, production, and holding of pharmaceutical products and determine a validation approach. The individual should have experience with current US and international regulations, guidance, industry best practice in one of the following areas of validation: facilities, utilities, and equipment qualifications, process validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the validation specialist must be approved by the client. | 08/21/2024 |
| 2678 | Quanta Therapeutics Radnor, PA Research Associate/Sr. Research Associate BS/MS in cancer biology/molecular/cell biology or related biomedical field Exp: 1-3 years |
A highly motivated, detail-oriented, hands-on biologist to contribute to existing programs and to initiate and develop new drug discovery efforts within Quanta. The ideal candidate will have a good understanding of cancer biology, signal transduction pathways, and hands-on experience in elucidating molecular mechanisms underlying tumorigenesis. He/she will work with a collaborative team and contribute to the Company’s pipeline. | 08/21/2024 |
| 2679 | QuidelOrtho Raritan, NJ Quality Control Scientist I Bachelor’s degree in medical technology, Biology, Chemistry or a related field of study Exp: 1-3 years |
As the company continues to grow as QuidelOrtho, we are seeking a QC Scientist I. The QC Scientist I will be responsible for testing stability and final product release of all OCD products. This person will assure compliance with company standards and applicable regulatory agencies. They will participate in failure investigations to help determine root cause, track and trend data, identify and suggest process improvements to improve business measures. This position will be onsite full-time at our Raritan, NJ office. | 08/21/2024 |
| 2680 | QuidelOrtho Athens, OH Associate Biochemist Bachelor’s Degree in a biology, biochemistry, chemistry or other related science field Exp: 1 year |
The Associate Biochemist is responsible for the production and quality testing of various raw material, intermediate components and finished good catalog items, in accordance with Quidel’s Quality System Regulations. This role is located in Athens, Ohio. | 08/21/2024 |
| 2681 | QuidelOrtho Athens, OH Quality Engineer B.S. Degree in Chemistry, Biochemistry, Biology, Engineering, or a related discipline. Exp: 1-3 years |
The Quality Engineer provides support to Quality and Operations on all aspects of the manufacturing process. The position will work to resolve quality issues by ensuring adequate root cause investigations conducted and verifying effectiveness of CAPAs implemented. The position will utilize key Quality Engineering principles, tools, and practices to develop and optimize process controls and quality system processes and identify opportunities to improve quality and cost that are aligned with the overall business goals and QuidelOrtho’s Quality Policy. The position will assess risk and will drive quality related decisions. This role is located in Athens, Ohio. | 08/21/2024 |
| 2682 | QuidelOrtho Athens, OH Associate Molecular Biochemist BA/BS or MA/MS in life sciences-related field. Exp: 1-3 years |
The Associate Molecular Biochemist plays a crucial role in GMP molecular chemistry production and in-process quality testing activities. Responsibilities include molecular biochemistry production and quality testing. The Associate Molecular Biochemist will perform routine procedures with senior staff oversite. Some collaboration with senior staff on investigations and troubleshooting is expected. This role is located in Athens, Ohio. | 08/21/2024 |
| 2683 | Quintara Discovery Hayward, CA Senior Research Associate Master’s degree in Biology or related field. Exp: 1 year |
Responsible for exercising independent judgment in conducting research on in vitro ADME screening (ADME: Absorption, Distribution, Metabolism, and Elimination): Plan experimental approaches; Design and carry out bioanalytical tests of various compounds for the potential development of human therapeutics; Analyze and interpret experimental data and prepare reports of findings. Design and perform procedures in ADME assay projects by operating lab equipment, including integrated hardware, software, optical and fluidic subsystems; Conduct sample bioanalysis and develop bioanalytical methods for the quantitative analysis by using mass spectrometry; Document information on procedures, modifications, and methods; maintain records of experiments and results in the accessible format. | 08/21/2024 |
| 2684 | Quotient Sciences Boothwyn, PA Validation Engineer ??Bachelor’s degree in Engineering, Information Systems, or a related field of study preferred Exp: 0-5 years |
The Validation Engineer is responsible for providing engineering support for maintenance and validation activities while managing regulatory requirements around methodology and protocols for pharmaceutical manufacturing. | 08/21/2024 |
| 2685 | Qx Therapeutics New Haven, CT Scientist 1 Bsc, or Msc degree in a biological/pharmacology discipline. Exp: 0-5 years |
This is an opportunity to work on cutting edge science to tackle diseases related to acute lung injury. We are looking for a scientist who brings enthusiasm, intellectual curiosity, scientific rigor and a desire to innovate new medicines for patients. Assume responsibility for in vivo studies to advance our lead development programs, including study planning, protocol design, study execution, data analysis and study report writing. Implement good documentation practices. Manage in vitro biological assay development and execution. Manage in vivo model development and characterization. Analysis of experimental data and draft study report. Effectively collaborate with a fully integrated team to facilitate the success of projects. Assume part of project management work for the organization. | 08/21/2024 |
| 2686 | Bio-Techne Minneapolis, MN Research Associate, Protein Purification GMP Bachelor’s degree in biochemistry, biotechnology, or equivalent Exp: 0-2 years |
This position is responsible for purifying proteins and polyclonal/monoclonal antibodies in a GMP Lab, following GMP guidelines. This includes, but is not limited to GMP, ACFP, natural, and other products used by pharma and IVD customers. Purifies proteins and polyclonal/monoclonal antibodies by column chromatography, using a variety of techniques and equipment. Filter, aliquot, and bottling of product using aseptic techniques, and submits to bulk inventory. Documents batch records following GMP guidelines. | 08/21/2024 |
| 2687 | Bio-Techne San Marcos, CA Chemistry Associate Bachelor’s degree in Chemistry, Biochemistry, Biological Science, or related field Exp: 0-2 years |
By joining Bio-Techne, San Marcos you’ll join a proven leader in the Manufacturing of In-Vitro Diagnostics. Our Research Associates are focused on the product development of diagnostic assays, to include reagents, calibrators, controls, calibration verifiers and proficiency testing. When you join us, you will be part of a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all its brands, provides tools for researchers to further treat and prevent disease worldwide. Responsible for processing and formulation of controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for manufacturing quality products on schedule. General knowledge and basic application of concepts, theories, terminology, and practices that apply to manufacturing in a laboratory environment. | 08/21/2024 |
| 2688 | Nova Biomedical Waltham, MA Quality Engineer I BS degree in engineering, the sciences, or another technical discipline. Exp: 1-2 years |
Nova Biomedical is hiring a Quality Engineer I on-site (hybrid) in our Waltham, MA facility. This role will support Quality Assurance activities within the corporate Quality Management System (QMS). Responsibilities include providing expertise and general oversight for the management and improvement of design and development, validations, quality planning, internal auditing, investigations, process controls, change management, quality records, corrective and preventive activities, data management, employee training, and other duties as assigned. | 08/06/2024 |
| 2689 | Novartis San Diego, CA Research Scientist - In Vitro Pharmacology B.S. in molecular biology, cell biology, biochemistry, bioengineering, or related scientific discipline Exp: 0+ years |
We are seeking a highly skilled and motivated Research Scientist I to join our dynamic in vitro pharmacology team In San Diego dedicated to advancing gene therapy and siRNA for neurological and neuromuscular diseases. As a key member of our research team, you will play a critical role in supporting various aspects of research including tissue sample processing, biodistribution, biomarker assay development, antibody screening campaigns, as well as oversee lab operation activities. Join us in our mission to transform the treatment landscape for neurological and neuromuscular diseases through cutting-edge gene therapy approaches. Apply now to make a meaningful impact on the lives of patients worldwide! | 08/06/2024 |
| 2690 | Novasenta Pittsburgh, PA Research Associate, Assay Development Master’s Degree or bachelor’s degree from an accredited institution Exp: 1+ years |
Conducts routine and non-routine lab procedures and assays for molecular, cellular, and metabolic characterization of relevant samples from mouse models of cancer and human clinical cancer tissue. This includes the conduct of relevant exploratory experiments and control experiments, applying basic scientific principles. As needed, supports the development and validation of new technologies for molecular, cellular and metabolic characterization of samples. Supports the development of biological, immunological assays to investigate mechanisms of immune-mediated effects of novel identified targets. Contributes to the profiling and validation of novel, druggable, immunotherapy targets. Documents and maintains a detailed and precise record of work performed. Performs lab management, which includes ordering supplies and maintaining inventory, ensuring safety, service and maintain laboratory instruments of the lab,etc. Atively participates in the scientific dialogue of the group and proactively collaborates with colleagues. Performs all other duties as assigned | 08/06/2024 |
| 2691 | Novavax Gaithersburg, MD Research Associate II Bachelor’s or Master’s degree in Immunology/Virology or relevant field Exp: 1+ years |
We are seeking a highly motivated individual to serve as a Research Associate who takes on the responsibility in support of study projects on cellular assays for Adjuvant and Vaccine candidates. This position will require the incumbent to develop and qualify assays for analyzing samples from preclinical and clinical studies, mainly by using Flowcytometric staining, but can extend to other cellular assays such as Elispot and cytotoxicity assay. This position will mostly involve hands-on laboratory work. | 08/06/2024 |
| 2692 | Novavax Gaithersburg, MD Research Associate II - Vaccine Immunology B.S. or M.S. in Immunology, Biology, Molecular Biology, Virology, Genetics or related field. Exp: 1+ years |
Novavax, Inc (Nasdaq:NVAX) is a biotechnology committed to helping address serious infectious diseases globally through the discovery, development and delivery of innovative vaccines to patients around the world. We have more than a decade of experience contending with some of the world’s most devastating diseases, and we are here to make a difference. Hard-won lessons and significant advances illustrate that our proven technology based on solid science tested by decades of research, has tremendous potential to make a substantial contribution to public health worldwide. | 08/06/2024 |
| 2693 | Novavax Gaithersburg, MD Analytical Development Associate I/II (Contract) Bachelor’s degree OR Master’s degree Exp: BS: 1-2 years or Master's: Some industry internshnip or co-op exp |
Novavax is seeking an Associate II, Analytical Development to provide technical and documentation support in a laboratory setting. This role is responsible for contributing to the method development, qualification, and technology transfer for analytical methods. The qualified individual will bring experience in relevant analytical technologies, such as ELISA, SRID, Luminex, or BLI. The position will perform in-process testing, as needed, to support the Process Development, Formulation Development, and Manufacturing teams, in addition to method development and qualification. | 08/06/2024 |
| 2694 | Novitium East Windsor, NJ Specialist Preventive Maintenance Bachelor’s in Instrumentation / industrial / electronics / electrical / mechanical / related Exp: 6+ months |
Responsible for developing and carrying out a scheduled preventive maintenance program for plant utilities and manufacturing equipment; Troubleshoot existing equipment for issues, change or modify to improve efficiency; Work closely with EHS to maintain facility compliance with applicable OSHA and DEP regulations; Prepare and assist Plant Shut-Down plans and coordinate with all departments to execute the plans; Develop, maintain, and oversee Spare Parts Inventory system and its procurement in collaboration with Purchasing Manager; Manage the organization and maintenance of spare parts warehouses and workshops; Set in service for an existing system to manage Work Orders; Discuss heating/cooling system malfunctions with users to isolate problems or to verify that problems have been corrected; Record and report all faults, deficiencies and other unusual occurrences as well as time and materials expended on work orders. | 08/06/2024 |
| 2695 | Novitium East Windsor, NJ Regulatory Specialist Bachelors in Pharmaceutical sciences / biology / microbiology / chemistry / chemical / Regulatory Affairs Exp: 1+ years |
Review, manage and write regulatory submissions electronically which include New ANDA filings, Complete Response letters, Information requests, Amendments to the ANDA’s (Labeling, Chemistry & Bioequivalence) of different dosage forms (Tablet, Capsule, Liquid & Solutions); responsible for filing the Post Approval Supplements like CBE-0, CBE-30 (Changes being effective in 30 days) and Prior Approval Supplements (PAS); submitting dossiers electronically after the approval of initial product submissions (ANDA); review of the leachable and extractable reports generated for the oral Liquid & Solution drug products. | 08/06/2024 |
| 2696 | Novitium East Windsor, NJ Sr. Software Engineer Master’s in computers / electronics / electrical / related Exp: 6+ months |
Design and implement Netapp storage systems, including installation, configuration, software upgrades, and storage provisioning; deploy NetApp tools (OCUM,WFA,DFM,snapcreator) to support production operation; configure ifgroups, IPSapce, Vlan’s and Braodcast domains; administer Fiber Channel SAN fabrics, including installation, configuration, zoning, software upgrades, and maintenance of switches; responsible to code and maintain system scripts to support operations of the storage systems; perform architectural planning, designing, coding, and prepare test plans; deploying & configuring new virtual systems and ecosystems. | 08/06/2024 |
| 2697 | Novitium East Windsor, NJ Instrumentation Engineer Bachelor’s in Instrumentation / industrial / electronics / electrical / mechanical / related Exp: 6+ months |
Responsible for Instrument and Equipment’s of entire Plant; Installation, troubleshooting & calibration of instruments such as TOC Analyzer, HMI, PLC, Flow Meters, Temperature controller, transmitter, pressure transmitter, gas analyzer; Maintaining minimal instrument downtime through troubleshooting & maintenance activities; Maintaining data backup, instrument documentation, and Spares Inventory & Annual Maintenance contracts; Pro-active Support for Quality Control, Production & Compliance group’s activities; Follow-ups and closures of instrument Change controls, deviations instrument related incidents, & CAP A (corrective and preventive action); Procurement of qualified equipment’s as per GLP & Pharmacopeia requirements, and responsible for IQ, OQ, DQ and PQ for instruments and manage all paperwork. | 08/06/2024 |
| 2698 | Novitium East Windsor, NJ Quality Control Analyst Bachelors in Pharmaceutical Sciences / Biology / Chemistry / Microbiology / Chemical / Related Exp: 1+ years |
Conduct research, analysis, synthesis, and experimentation on substances, for such purposes as product and process development and application, quantitative and qualitative analysis, and improvement of analytical methodologies; conduct testing and analysis of pharmaceutical raw materials like drug substance, excipients and packaging materials to analyze various parameters like assay, dissolution, impurities, related substances, residual solvents using various technical instruments like HPLC, GC, UV spectrometry; Conduct testing and analysis of finished product for different dosage forms like capsules, tablets, powder for oral suspension and solutions. The dosage forms include food supplements like vitamin capsules, mineral tablets, and multivitamin syrups. | 08/06/2024 |
| 2699 | OraSure Technologies Bethlehem, PA Formulations Specialist Bachelor of Science in chemistry, biochemistry, or equivalent sciences Exp: 1-3 years |
The formulations specialist manufactures chemical formulations necessary for production of finished goods, documents production information, and performs routine maintenance on equipment/machinery. | 08/06/2024 |
| 2700 | Novonesis Wausau, WI Process Engineer Bachelor of Science degree in Engineering Exp: 1-3 years |
This position works under general direction and is primarily responsible for developing and improving manufacturing processes by studying product and manufacturing methods. The Process Engineer is responsible for commissioning manufacturing equipment and ensuring equipment operates and performs as intended. | 08/06/2024 |
| 2701 | Novonesis Franklinton, NC Process Engineer I BS or MS in Engineering Exp: 0+ years |
You will have the opportunity to work closely with production to ensure things operate smoothly and efficiently. You will be able to drive process improvements, work with capital projects, and support upscaling new processes from development. | 08/06/2024 |
| 2702 | Noxilizer Hanover, MD R&D Lab Scientist Bachelor’s degree in Biology, Biotechnology, Biomedical Engineer, Material Science or related field preferred. Exp: 1+ years |
The R&D Lab Scientist is responsible for performing, documenting and reporting microbiological sterilization studies for Noxilizer’s customers. Noxilizer’s customers range from Fortune 500 pharmaceutical, biotech and medical device companies to start-ups that are in the US, Europe and Asia. These studies are the first critical step in the customer’s evaluation of nitrogen dioxide sterilization and their product, as well as an important revenue-generating area for the company. The R&D Laboratory Scientist will join a high-performing team of experts to solve sterilization challenges while they grow their skills for future career opportunities. | 08/06/2024 |
| 2703 | Globus Medical West Carrollton, OH Associate Engineer, Manufacturing Bachelor's Degree in Electrical Engineering Exp: 0-2 years |
As part of the manufacturing team, the Associate Manufacturing Engineer needs to have strong technical skills, be hands-on, and be creative with minimum supervision. The job requires a team player with the ability to function well in a challenging, fast-paced environment. This person must be enthusiastic, positive, even-tempered, and have strong skills in areas of communication, dependability, interpersonal relationships, flexibility, and maturity. | 08/06/2024 |
| 2704 | Ocular Therapeutix Bedford, MA Microbiology Analyst I B.S. degree in Microbiology, Biology or related scientific field. Exp: 1 year |
The Microbiology Analyst I is responsible for performing QC activities in microbiology lab such as Environmental Monitoring of the cleanrooms and support in performing testing of product and raw materials according to established specifications and procedures. This position also manages EM excursions and data entries. | 08/06/2024 |
| 2705 | Ofni Systems Raleigh, NC Computer Systems Validation Engineer BS or equivalent degree in math, science or engineering Exp: 1 year |
We are hiring a Validation Engineer to be on the cutting edge of automated validation techniques. You will be responsible for implementing our validation solutions while working with industry-leading companies. Ideal candidates are experts on the requirements of 21 CFR 11, have excellent critical thinking and interpersonal skills, and are motivated to meet client needs for compliance. If you are an A-level engineer who enjoys the challenge of solving real-world compliance problems then we would like to talk with you. | 08/06/2024 |
| 2706 | OncoPep Cambridge, MA Research Associate (In Vitro) BS Exp: 1 year |
We are looking to expand our Research team by recruiting a skilled Research Associate in cellular/molecular biology to join our growing team. The candidate will primarily work with molecular and cell biology techniques including culture of primary cells and cell lines, flow cytometry, ELISA, and western blot. He/She will play an important role in the discovery and development of novel biotherapeutics for immuno-oncology. He/she will be responsible for generating the tools necessary for evaluation and screening of lead candidate therapeutics. He/she will be expected to participate in experimental design, conduct experiments, optimize throughput, maintain detailed records, and generate standard operating procedures. | 08/06/2024 |
| 2707 | Orbital Therapeutics Cambridge, MA Research Associate, Molecular Immunology B.S. or M.S. in Immunology, Biology, or related field. Exp: 1-4 years |
Orbital Therapeutics is currently seeking a highly motivated, self-driven, and creative individual with extensive experience in molecular immunology, looking to join an outstanding research team dedicated to designing and executing studies using a new generation of RNA medicines. This individual will enjoy working in a pioneering, fast-paced, and collaborative start-up environment with the opportunity to coordinate studies focused on immunomodulation, while also exploring ways to unleash the power of Orbital’s core technologies. This individual will join a culture of intellectual rigor, scientific curiosity, and collegiality, cross functionally contributing to research across the organization. The candidate will be an important team member whose contributions will be critical to our success in developing new therapeutics to improve the lives of patients. | 08/06/2024 |
| 2708 | Organogenesis Norwood, MA QC Analyst I-Cell Culture Bachelor’s degree in biology or related field Exp: 1-3 years |
The QC Analyst I, Cell Culture performs quality activities in support of product production and release for ASA Product. This position interacts with other internal departments, including Production, Quality Assurance, Validation, Calibration, Materials, and Logistics. The position also interacts with external entities including contractors and suppliers. The QC Analyst I performs a variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending, and reporting results. | 08/06/2024 |
| 2709 | Organogenesis Norwood, MA QC Analyst I - Chemistry Bachelor’s degree in biology or related field Exp: 1-3 years |
The QC Analyst I, Chemistry performs quality activities in support of product production and release for ASA Product. This position interacts with other internal departments, including Production, Quality Assurance, Validation, Calibration, Materials, and Logistics. The position also interacts with external entities including contractors and suppliers. Performs a variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending, and reporting results. | 08/06/2024 |
| 2710 | OriGen Biomedical Austin, TX Quality Engineer I Bachelor’s degree in Engineering Exp: 1-2 years |
The Quality Engineer I is responsible for technical duties within the Quality organization including validation and qualification, calibration, and customer contact. These duties will support manufacturing operations, customer service, process improvement, and regulatory requirements. | 08/06/2024 |
| 2711 | Packgene Biotech Houston, TX Quality Control Specialist I - HPLC Bachelor's degree in bioscience, chemistry or related field Exp: 1-2 years |
The Quality Control Specialist I or II- HPLC will undertake laboratory work under the guidance of senior scientists. The Quality Control Specialist I or II is responsable to operate and maintain HPLC instruments; execute HPLC assays. The Quality Control Specialist I will have chance to learn Gene Therapy concepts and cGMP practice, etc | 08/06/2024 |
| 2712 | Padagis New Hope, MN QC Chemist II Bachelor's degree Exp: 1+ years |
We are hiring for a QC Chemist II, 2nd Shift, in New Hope, MN who performs inspection on a range of work to detect defects and maintain quality standards. The hours for this role are Monday through Friday 2pm-10pm with some flexibility. | 08/06/2024 |
| 2713 | Endo Rochester, MI Quality Associate Specialist, Product Release (Midnight shift) BA/BS degree in a related discipline Exp: 0-1 years |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. All incumbents are responsible for following applicable Division & Company policies and procedures. | 08/06/2024 |
| 2714 | Endo Rochester, MI Quality Associate Specialist, Product Release (Days) BA/BS degree in a related discipline Exp: 0-1 years |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. All incumbents are responsible for following applicable Division & Company policies and procedures. | 08/06/2024 |
| 2715 | Endo Horsham, PA Quality Associate Specialist, MQA BA/BS degree in a related discipline Exp: 0-1 years |
The Quality Associate Specialist, under close supervision, performs routine collection of environmental and utility monitoring samples. This role also reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. May participate in “on the floor” activities during product manufacturing. | 08/06/2024 |
| 2716 | Paradromics College Station, TX Preclinical Research Assistant Bachelor’s or Master’s degree in Science or Engineering Exp: 1+ years |
The Paradromics Neuroscience team is seeking strongly motivated Research Assistants to contribute to the preclinical testing of our Connexus® Direct Data Interface in large animal models. This role is a temporary position with a fixed period of a year with the possibility of renewal at the end of the contract. This role involves interfacing with veterinarians, neuroscientists, electrical engineers, software engineers, and data engineers. Excellent communication and interpersonal skills are crucial for excelling at this role. This role requires an individual with a “can-do,” self-starter attitude. This position is based on-site in College Station, Texas. We are building next-generation brain implants to treat serious conditions in mental and physical health. If you want to use your skills in a positive, impactful way, if you like to be intellectually challenged, and if you want to be surrounded by hard-working and passionate co-workers, this work will be highly fulfilling. | 08/06/2024 |
| 2717 | Paragon 28 Englewood, CO Associate Quality Engineer - Rotational Bachelor’s in engineering or technical discipline Exp: 0-2 years |
The Rotational Associate Quality Engineer has varied responsibilities to assist both the Quality-Production and Quality-Design teams in ensuring Paragon 28’s compliance to regulations and standards. The role will split time and/or rotate through day-to-day tasks and exposure to the supplier quality engineering, design quality engineering and production quality engineering roles at Paragon28 for a 12-month period, with the intention of aligning a candidate’s skills and passion with business needs for permanent placement within the quality department | 08/06/2024 |
| 2718 | PCI Pharma Philadelphia, PA Process Engineer-AM Weekends Bachelor's Degree in mechanical, packaging engineering, or in a related field of study. Exp: 1-5 years |
We are looking for a dedicated process engineer to provide technical leadership for new product launches and lead continuous improvement activities. You will also identify and mitigate packaging issues for existing business through strong engineering and process improvement methods. All activities are focused around technical and operational support to production, maintenance, and support staff to include but not limited to: process improvement, equipment modification, optimization, safety, quality improvement, and increasing throughput. The process engineer will achieve this through delivery of tracking, analysis of metrics and project management. The ideal candidate will have a strong understanding and utilization of good engineering practices with the usage of lean six sigma techniques. The process engineer will also provide excellent organizational and leadership skills to determine staffing projections, equipment needs, equipment purchase, equipment installation, component layout, and line layout. **This is a weekends position. Friday, Saturday, & Sunday 7am to 7pm.** | 08/06/2024 |
| 2719 | PCI Pharma Philadelphia, PA Process Engineer I-2nd Shift Bachelor's Degree in mechanical, packaging engineering, or in a related field of study. Exp: 1-5 years |
We are looking for a dedicated process engineer to provide technical leadership for new product launches and lead continuous improvement activities. You will also identify and mitigate packaging issues for existing business through strong engineering and process improvement methods. All activities are focused around technical and operational support to production, maintenance, and support staff to include but not limited to: process improvement, equipment modification, optimization, safety, quality improvement, and increasing throughput. The process engineer will achieve this through delivery of tracking, analysis of metrics and project management. The ideal candidate will have a strong understanding and utilization of good engineering practices with the usage of lean six sigma techniques. The process engineer will also provide excellent organizational and leadership skills to determine staffing projections, equipment needs, equipment purchase, equipment installation, component layout, and line layout. *This is a 2nd shift position. The hours are 3pm to 11pm, Monday to Friday. | 08/06/2024 |
| 2720 | PCI Pharma San Diego , CA QA Specialist - Sterile Fill & Finish Bachelor’s degree Exp: 1-2 years |
This full-time position will report to the Quality Manager - Sterile Fill Finish focusing on supporting the Quality department with review and release of executed batch records, product inspection, product or raw material release, document control, production monitoring, environmental monitoring, tracking quality metrics and assisting with validations, preventative actions, audits and continuous improvement. This position is responsible for performing quality activities within the Sterile Fill and Finish group in accordance with all applicable procedures, regulations, and safety directives. This individual’s primary job function will be review and release finished lots of drug product vials and syringes manufactured by PCI. Other job functions may be required at the discretion of management and include but are not limited to drafting procedures, sampling raw materials or finished products, assisting in general operations of the zero human intervention isolators all in accordance with GMPs and established SOPs | 08/06/2024 |
| 2721 | Pel-Freez Biologicals Rogers, AR Quality Control Technician Bachelor's degree in science Exp: 1 year |
Under supervision, the QA Technician I will perform quality control testing and assist with the implementation of the Pel-Freez quality management system in accordance with ISO 9001. The role will be required to understand and promote the Quality System as part of the Company's overall goal toward continual improvement through strict adherence to all company policies, procedures, principals, and values. | 08/06/2024 |
| 2722 | Penumbra Alameda, CA Manufacturing Engineer II BS degree in Mechanical, Biomedical, Chemical, or Materials Engineering, or a related discipline required Exp: 1+ years |
As a member of the Manufacturing Engineering group at Penumbra, you will be called upon to solve complex problems and implement innovative solutions. You will provide manufacturing technology and robust solutions aimed at commercializing new products and continuously improving production processes. Working cross-functionally with engineering groups across the company, as well as with Production, Quality Control and Quality Assurance, you will resolve problems encountered on the production floor and throughout the business, and will apply your engineering knowledge and creativity to implement adaptations and modifications to the production line and to quality systems. | 08/06/2024 |
| 2723 | Penumbra Alameda, CA Manufacturing Engineer II BS degree in Mechanical, Biomedical, Chemical, or Materials Engineering, or a related discipline required Exp: 1+ years |
As a member of the Manufacturing Engineering group at Penumbra, you will be called upon to solve complex problems and implement innovative solutions. You will provide manufacturing technology and robust solutions aimed at commercializing new products and continuously improving production processes. Working cross-functionally with engineering groups across the company, as well as with Production, Quality Control and Quality Assurance, you will resolve problems encountered on the production floor and throughout the business, and will apply your engineering knowledge and creativity to implement adaptations and modifications to the production line and to quality systems. | 08/06/2024 |
| 2724 | Penumbra Alameda, CA Quality Engineer I Bachelor’s or Master's degree in an engineering or scientific discipline required Exp: 1+ years |
As a Quality Engineer I, you will be charged with the quality behind Penumbra's game-changing medical devices used to address some of the world's toughest disease states! Unlike quality engineering roles in other companies, at Penumbra, we provide our quality engineers with highly technical problems to solve. Your efforts will directly impact the safety of patients around the world who use our products. You will apply your passion for creative problem solving throughout all stages of the process, from concept to commercialization and into continuous improvements. | 08/06/2024 |
| 2725 | Performance Validation Grand Rapids, MI Level I/II Validation Engineer/Specialist BS degrees in Biomedical Engineering, Chemical Engineering or Mechanical Engineering Exp: 1+ year |
Performance Validation is seeking a full-time Level I or Level 2 Validation Engineer/Specialist to join our team in Grand Rapids, Michigan. Level I/II Validation Engineer/Specialist reports directly to the Division Director or Manager and will be assigned to one or more project teams headed by a Project Leader. | 08/06/2024 |
| 2726 | Pfizer Pearl River, NY Associate Scientist– Viral Vaccines & Immunology Bachelor's Degree in a relevant field of science Exp: 0-2 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role to generate high-quality immunoassay data in a regulated Good Laboratory Practices (GLP) setting to support Pfizer’s vaccine programs according to Standard Operating Procedures. You will support the preclinical evaluation and early clinical development of mRNA and protein based viral vaccines. You will perform various assays to monitor the immune responses elicited by respiratory virus, herpesvirus, and influenza virus vaccine candidates. In addition, you will maintain cell lines and prepare preclinical and early clinical samples for testing. Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. Your strong work ethic and collaborative spirit will be an integral part of our dynamic team. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. | 08/06/2024 |
| 2727 | Pfizer Pearl River, NY Associate Scientist - Sample Logistics and Solutions Bachelor of Science Degree or Bachelor of Arts Degree in a relevant scientific discipline Exp: 0-5 years |
The primary purpose of this job role is to function as a member of the Sample Logistics and Solutions (SLS) team within Pfizer Vaccine Research and Development (VRD). The incumbent will be responsible for receiving samples from global clinical/study trials according to approved protocols and processes. The individual will participate in all aspects of tracking and documenting the chain of custody of samples. The incumbent’s role will include sample receipt, documentation, storage, tracking, aliquoting, distribution to the testing labs, and sample disposal. The colleague will work in a team setting and will share roles and responsibilities as assigned by the team leader/manager. | 08/06/2024 |
| 2728 | NAMSA Northwood, OH Microbiology Technologist Bachelor Degree Exp: No Experience |
NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. Job Description: May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions, Accurately collects and records raw data in logbooks and on worksheets, May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures, May be required to perform required specific testing as applicable, May be required to operate specified laboratory equipment, May perform Environmental Monitoring, clean and disinfect cleanroom suites (required as applicable), Other duties as assigned. | 07/17/2024 |
| 2729 | NAMSA Minneapolis, MN Associate Pathology Technician Bachelor degree or equivalent in Biological Sciences or related discipline Exp: 0-2 years |
NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. Job Description: Supports or independently performs necropsy procedures, including complete necropsies and perfusion procedures. Assists and performs routine gross examination as required by GLP standards, and performs accurate and timely record keeping. Assists in coordinating and performing the shipping of all pathology related specimens to the appropriate designated facility. Performs thorough recordkeeping of shipping and receipt logs. Performs tissue trimming according to established guidelines. Performs photography and high-resolution x-ray imaging and film developing. Maintains proficiency in all appropriate designated departmental SOPs with knowledge of lab processes. Assists in the review of protocols that include pathology services, and assists with modifying pathology-related SOP’s. Maintains a clean, GLP-compliant lab and ensures all logbooks are reviewed and correct. Maintains laboratory equipment according to applicable SOPs. Performs calibration or validation activities to specialized equipment. Other duties as assigned. | 07/17/2024 |
| 2730 | NAMSA Minneapolis, MN Associate Pathology Technician Bachelor degree or equivalent in Biological Sciences or related discipline Exp: 0-2 years |
NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. Job Description: Supports or independently performs necropsy procedures, including complete necropsies and perfusion procedures. Assists and performs routine gross examination as required by GLP standards, and performs accurate and timely record keeping. Assists in coordinating and performing the shipping of all pathology related specimens to the appropriate designated facility. Performs thorough recordkeeping of shipping and receipt logs. Performs tissue trimming according to established guidelines. Performs photography and high-resolution x-ray imaging and film developing. Maintains proficiency in all appropriate designated departmental SOPs with knowledge of lab processes. Assists in the review of protocols that include pathology services, and assists with modifying pathology-related SOP’s. Maintains a clean, GLP-compliant lab and ensures all logbooks are reviewed and correct. Maintains laboratory equipment according to applicable SOPs. Performs calibration or validation activities to specialized equipment. Other duties as assigned. | 07/17/2024 |
| 2731 | NAMSA Irvine, CA Senior Lab Technician - Sterility Assurance Bachelor degree Exp: 1 years |
NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. Job Description:May perform various testing independently in accordance with SOPs and utilizing applicable work instructions, standards or guidelines. Performs routine calculations and may participate in analyzing and interpreting results. Maintain all test equipment and supplies for various testing. Clean glassware and prepare reagents for use in laboratory testing. Perform routine disposal of laboratory waste including disposal of test articles. Assist with making solutions and preparing reagents. Assist in the preparation of items for testing. Monitor raw materials and final finished media for conformance with applicable material specifications and SOPs. May be responsible for extractions, which may include: test article and control preparation, animal holding and preparation and solution preparation. May be responsible for chain of custody, delivery of samples, filing and sample distribution/shipping. Accurately collect and record raw data in logbooks and on worksheets. | 07/17/2024 |
| 2732 | NAMSA Irvine, CA Associate Microbiologist Bachelor degree Exp: 1 years |
NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. Job Description: Independently perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs, and according to applicable work instructions. Prepare or participate in the preparation of test specifications in conjunction with the requirements of the applicable standards and/or client instructions. May have direct client contact as needed. Responsible for review of incoming test articles and paperwork for appropriateness and accuracy and for taking all concerns to management as required. Accurately collects and records raw data in logbooks and on worksheets. Responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in SOPs. | 07/17/2024 |
| 2733 | Nanomix San Leandro, CA Associate Scientist, Assay Development Bachelor’s degree (or equivalent) in in Biology, Bioengineering, Chemistry, Chemical Engineering, or related field Exp: 0-2 years |
Nanomix has developed tests for the diagnosis of sepsis, acute kidney injury, and COVID-19, and is looking for an Assay Development Associate Scientist to help accelerate these programs and the development of other IVD assay products in the pipeline. This is an opportunity to work with a world class team to deliver an advanced, mobile medical diagnostic platform of urgent need to the healthcare industry. The successful candidate will apply scientific & technical skills in all phases of developing diagnostic assay products. Assist in developing Nanomix eLab biosensor cartridge assays to detect various biomarkers &/or viral/bacterial antigens. | 07/17/2024 |
| 2734 | Element Bend, OR Chemist I/Chemist II Bachelor’s Degree in Chemistry or related field is required. Exp: Some experience (for Chemist I) or 2 years experience (for Chem II) in a laboratory setting |
Element has an opening for a Chemist I or Chemist II position at our extractables and leachables (E&L) testing Center of Excellence in Bend, OR. This position will work in a cGMP-regulated environment under the direction of a Team Lead or other senior staff member in laboratory and office settings. The position will work with a team completing E&L project work using internal methods, protocols and SOPs according to customer specific requirements. This position requires working in a collaborative manner with other team members to accomplish organizational goals, providing ideas to improve efficiency and actively contributing to positive co-worker/customer relationships through efficient interaction on current projects. The Chemist I or Chemist II will also contribute to team continuous improvement initiatives. | 07/17/2024 |
| 2735 | Element Wixom, MI Project Manager - Engineer Bachelor of Science degree in a science or testing related field including but not limited to: Metallurgical Engineering, Materials Science, and Polym Exp: 0-5 years |
Element has an opportunity for an Engineer to join our rapidly expanding Project Management team in our Wixom, MI Lab. The Project Manager will be coached to be able to provide quotations, manage testing programs, write technical reports, and support the other team members. Our Engineers perform a variety of routine and non-routine testing assignments and insures timely and accurate test results under minimal direct supervision. The project manager position must be proficient in a number of core business and technical skills as well as compliance to established safety rules, code of conduct, and company policies and procedures. | 07/17/2024 |
| 2736 | Element Fremont, CA Electromagnetic Compatibility Compliance Engineer Bachelor’s Degree in Engineering Exp: 0-2+ years |
Element, has an opportunity for Electromagnetic Compatibility Compliance Engineer in the Regulatory Division of our Fremont, CA. This position applies engineering concepts for testing and evaluation of electronic and wireless RF devices for US federal and international regulatory compliance. Determining compliance requires the understanding and application of test standards, diagnosing problems, analyzing results, and troubleshooting unexpected performance in a fast-paced environment and industry. All training provided. | 07/17/2024 |
| 2737 | Element Huntington Beach, CA Associate Engineer Bachelor of Science degree in a science or testing related field Exp: 0-1 years |
Join us as an Associate Test Engineer and see how your variety of routine and non-routine testing make a difference and how critical it is to helping us deliver on our purpose and achieve our goals. Element is a world renown Aerospace Testing Company with clients such as Boeing, SpaceX and Blue Origin. At Element our shared purpose of ‘Making tomorrow safer than today’ is what brings us together. We are energized by our ambition to make the world a better place and create a safer future for people. This is what sets us (and you, if you join us…) apart from the crowd. | 07/17/2024 |
| 2738 | NantWorks Culver City, CA Battery Engineer B.S/M.S. in Mechanical Engineering, Chemical Engineering, Materials Science, or related technical field Exp: BS - 2 years; MS - 0+ years |
The Battery Engineer will be responsible for development, selection and validation active materials across the anode and cathode portfolio, assisting in development and implementation of R&D tools, and general engineering tasks. This includes developing and characterizing active/passive materials, developing slurry and coating recipes, building cells, and cell testing, leading engineering design and construction. This individual will be a key contributor in advancing NantG Power's competitive advantage to drive energy density, power density, safety, and materials sustainability improvements at scale. The ideal candidate will have a strong record of scientific achievement in the areas of Li-ion batteries, nanomaterials, and/or electrochemistry. | 07/17/2024 |
| 2739 | LGC Biosearch Technologies Alexandria, MN Quality Control Technician I - Laboratory Bachelor’s degree in a relevant scientific discipline Exp: 0-2 years |
The Quality Control (QC) Technician I focuses on the performance of analytical testing activities within the consumable product lines. They are responsible for testing intermediate and finished products, analysing the results of Quality Control testing and comparing results to established specification and/or customer requirements. In addition, they may perform testing and/or review of incoming goods. | 07/17/2024 |
| 2740 | LGC Biosearch Technologies Cumberland Foreside, ME Manufacturing Chemist I Bachelors degree in life science field or other related science or medical Exp: No Experience |
The Manufacturing Chemist I fulfills the essential role of preparing reagents, buffers, stocks, and other solutions using established procedures within the operations laboratory. They will use general laboratory equipment and techniques to perform these tasks under both direct and indirect supervision. They are expected to perform routine analysis and interpretation of test results against established acceptance criteria with limited judgment. | 07/17/2024 |
| 2741 | LGC Biosearch Technologies Middleton, WI Lab Services Technician Bachelor's degree in a scientific field of study (e.g. biology, chemistry, physics) Exp: 0+ years |
The Lab Services Technician provides foundational support to the processing and preparation of client samples for the Lab Services team at a specific operational site. In agreement with other Lab Services team members, this position is responsible for driving their operational duties by supervisor direction as well as standard operating procedures (SOPs) and work instructions. | 07/17/2024 |
| 2742 | LGC Biosearch Technologies North Charleston, SC Production Chemist I Bachelor of Science degree is required, chemistry degree preferred Exp: 0-2 years |
The Production Chemist I is responsible for the manufacturing of reference standard solutions by following routine procedures and operations of laboratory equipment. This is a highly collaborative position and requires a high level of teamwork and productivity. We are looking for individuals that can thrive in a fast-paced laboratory setting and demonstrate ability to prioritize and organize work with guidance from team leads and supervisor. Our site manufactures both catalog and custom solutions for customers requiring focused bench work, detailed record keeping and flexibility in daily tasks. | 07/17/2024 |
| 2743 | LGC Biosearch Technologies Petaluma, CA Oligonucleotide Production Technician - Liquid Handling Bachelors Degree or Master's Degree preferred in Life Sciences. Exp: 0-2 years |
The Oligonucleotide Production Technician I will perform tasks associated with the production of modified oligonucleotides in a high throughput time sensitive manufacturing environment in compliance with company procedures and external regulatory requirements. | 07/17/2024 |
| 2744 | Sotera Health Salt Lake City, UT Lab Analyst - Analytical Chemistry Bachelors Degree, relevant Life Science Exp: No Exp |
Laboratory Analysts conduct testing under supervised conditions in accordance with established procedures. Successful lab analysts are people who enjoy conducting tests following written instructions, who pay close attention to detail to make sure everything is done correctly, and who have high standards of personal integrity so that they deliver high-quality results. | 07/17/2024 |
| 2745 | Nemagen Discoveries Newark, NJ Research Scientist B.S. in a Biological Science orin a related field Exp: 0+ years |
NemaGen Discoveries’ mission is to advance therapies to treat mast cell-related and chronic inflammatory diseases. Under the direction of NemaGen’s Principal Scientist, you’ll work in an exciting and fast-paced start-up environment where you’ll assist with the development of NemaGen’s research programs. NemaGen is looking for candidates with a strong scientific background that have an interest in entrepreneurship and helping grow NemaGen in the coming years. If you want to be a part of cutting-edge research and improve the lives of patients, we encourage you to apply! Design and perform cell culture assays related to the development of innate immune cells with novel chemical compounds. Phenotypically and functionally characterize the activation state of various immune cell populations. Perform in-vitro efficacy studies. Operate standard laboratory equipment including, but not limited to, centrifuges and flow cytometers. | 07/17/2024 |
| 2746 | AstraZeneca Santa Monica, CA Associate, Quality Control Analyical BS in biological sciences or a related field is required. Exp: 0+ years |
Neogene is looking for an energetic and experienced person with cell therapy quality control background to join our Quality Control (QC) team. You will contribute to the advancement of our product pipeline by performing QC analytical method qualification, complete sample analysis and other assigned tasks. You will also independently organize and present results and conclusions. You will ensure that the QC Analytical laboratory is operating as expected. | 07/17/2024 |
| 2747 | NeoGenomics Laboratories Durham, NC Molecular Laboratory Technologist, Temporary Bachelor’s Degree in one of the chemical, physical, or biological sciences Exp: 1+ years |
The Laboratory Technologist works under minimal supervision and consistently and independently performs the complex level of clinical tests by following department procedures. You will drive initiative for prompt, accurate performance of test results with appropriate documentation of result. | 07/17/2024 |
| 2748 | Neolight Scottsdale, AZ Biomedical Engineer Bachelor's or Master's Degree in Electrical Engineering Exp: No Experience |
We seek a full-time entry-level Biomedical Engineer focusing on Electrical Engineering. In this role, you will provide strong, independent technical support to teams that contribute to resolving significant electrical and embedded system issues for the next generation and on-market products. A successful candidate will be a productive individual contributor who works independently with general supervision on larger, moderately complex projects/assignments. In addition, the candidate sets objectives for their job area to meet the objectives of projects and assignments. | 07/17/2024 |
| 2749 | Neuralink Austin, TX Associate Chemist Bachelor OR M.S. of Science in Chemistry, Biochemistry, or a related field Exp: 1-2 years |
The Associate Chemist role will work with teams across the Neuralink organization to analyze the chemical and biological characteristics of manufacturing processes and finished devices. This will include various levels of product testing during R&D and release to obtain data that may be required for product approvals. Additionally, this data may be used to confirm patient safety of our products by applicable global regulations, regulatory guidelines, or voluntary consensus standards. Daily responsibilities may involve drafting internal procedures and test protocols, sample preparation, laboratory testing, method development, inventory management, and other miscellaneous laboratory tasks. The primary goal will be to assist in medical device chemical and biological characterization to support patient safety and regulatory approval. | 07/17/2024 |
| 2750 | Revvity San Diego, CA Biochemist I - Proteogenomics Bachelor’s degree in Physical Sciences, Life Sciences, or other related fields Exp: 1+ years |
BioLegend (a division of Revvity, Inc.) has an opening for a self-motivated individual with production experience in a fast moving and dynamic environment to join our Proteogenomics team! The biotechnician will be an integral member of a team, that manufactures and provides high-plex oligonucleotide conjugated antibodies panels to enable studies for novel applications in precision medicine, oncology, immunology, neuroscience, and stem cell research. This position will report to a team lead and will ensure the highest quality of our finalized antibody products. This is a great opportunity to work in a fast-paced and dynamic environment for you to enhance your knowledge in the biotechnology industry! In this position you will perform column chromatography manually and via automation, troubleshooting of problematic errors, continue to improve methodologies for efficiency, follow Standard Operating Procedures (SOP)s, and cross train on a variety of other supporting tasks. | 07/18/2024 |
| 2751 | Revvity San Diego, CA Research Associate I - Immunoassay (LEGENDplex BS in a Biology, Chemistry or other related field Exp: 1+ years |
This position is responsible for supporting immunoassay products development and manufacturing in the Biomarker Immunoassay group. The Research Associate will be involved in all aspects of the product development processes including designing, initiating, testing, troubleshooting, testing materials manufacturing, technical instruction transferring, and product launching. More specifically, he or she will be working with an experienced scientist on testing new hybridoma clones, qualifying the raw materials used for immunoassay products manufacturing and new immunoassay product development and launching. These immunoassay products may allow simultaneously detection of up to 13 important biomarkers for inflammatory diseases, stem cells, cancer, cardiovascular disease or neuron degenerative diseases, and will be very useful tools for the biomedical research community. This position is a great opportunity for gaining working experiences in growing business in a fast-pace biotech industrial environment. He or she will be able to manage the assigned function and tasks with great communication skills in a timely manner with independence after appropriate training. | 07/18/2024 |
| 2752 | Revvity San Diego, CA Research Associate II - Immunoassay (LEGENDplex) BS in a Biology, Chemistry, or other related field Exp: 1+ years |
This position is responsible for supporting immunoassay product development and manufacturing in the Biomarker Immunoassay group. The Research Associate will be involved in all aspects of the product development processes including designing, initiating, testing, troubleshooting, testing materials manufacturing, technical instruction transferring, and product launching. More specifically, he or she will be working with an experienced scientist on testing new hybridoma clones, qualifying the raw materials used for immunoassay products manufacturing and new immunoassay product development and launching. These immunoassay products may allow simultaneous detection of up to 13 important biomarkers for inflammatory diseases, stem cells, cancer, cardiovascular disease, or neuron degenerative diseases, and will be very useful tools for the biomedical research community. This position is a great opportunity for gaining working experience in growing business in a fast-paced biotech industrial environment. He or she will be able to manage the assigned function and tasks with great communication skills in a timely manner with independence after appropriate training. | 07/18/2024 |
| 2753 | Revvity San Diego, CA Biochemist I - GMP Beads Conjugation BS degree in chemistry/biochemistry, material science or life science. Exp: 0-1 years |
This biochemist role will be an integral member of our GMP team that develops and manufactures BioLegend’s regulated magnetic beads and antibody reagents produced in our US FDA registered cGMP manufacturing facility. This position will report to a GMP MOJO Scientist. The desired candidate must be a team-player who is organized and is able to work in a fast-paced environment to meet deadlines. Great attention to detail is also a skill that will allow the candidate to be successful. | 07/18/2024 |
| 2754 | Revvity San Diego, CA Research Associate I - Molecular Cloning Bachelors of Science in Biological Sciences Exp: 1+ years |
This position is responsible for developing recombinant protein/antibody research products in the Molecular Cellular Biology group. The research associate will be involved in the early stage of product development for recombinant protein/antibody products. The duties include preparing cell culture media, DNA purification, PCR and molecular cloning, bacterial and mammalian cell cultures, and purifying recombinant proteins/antibodies with several affinity tags, and weekly presentations of results to internal and external groups. This position offers a significant opportunity for learning molecular biology techniques and career growth in the biotechnology industry. | 07/18/2024 |
| 2755 | Revvity San Diego, CA Quality Control Associate I Bachelor’s degree in a scientific discipline Exp: 1+ years |
At BioLegend we are dedicated to commercializing high quality reagents to support the research community for legendary discoveries. The Associate for BioLegend’s Quality Control group will test products such as antibodies and proteins in the following application(s): flow cytometry, immunohistochemistry, western blotting, ELISA, multiplex immunoassays and/or functional bioassays. The candidate will perform all aspects of the assays following SOPs and ISO requirements. Additional responsibilities include culturing mammalian cell lines, isolating primary cells, and maintaining laboratory equipment and supplies. We are looking for a highly motivated person who loves science and wants to be part of a dynamic and fast paced team. | 07/18/2024 |
| 2756 | Revvity Boston, MA Associate Chemist B.S. degree in Chemistry, Biochemistry, Chemical Engineering Exp: 0-2 years |
We are seeking an Associate Chemist to join our team of scientists in the Research Reagents group manufacturing synthetic chemical products used throughout the world in scientific research applications. The Associate Chemist will also have an opportunity to work on the Microfluidics product line. This position will function as a member of the production staff and will participate in the transfer, implementation and on-going production of products in the laboratory. This is an on-site role based at our Boston South End manufacturing site. | 07/18/2024 |
| 2757 | Neurona Therapeutics South SF, CA Research Associate, Process Sciences Bachelor’s or master’s degree in chemistry, biology or biochemistry. Exp: 0-5 years |
Our ideal candidate is a self-motivated individual who has a passion for method development and qualification that can thrive in a fast-paced dynamic environment. The successful candidate will work as a member of the Process Sciences department and will be responsible for projects requiring design and qualification of process equipment. In addition, the candidate will interface with Manufacturing, Process Science, Facilities, Validation, QA, and Contract Engineering/vendor firms to produce detailed designs for procurement, construction, installation, start-up, and validation of process systems including systems for shipping product to clinical sites. This is a fantastic opportunity to join a small team, work on transformative science, and take part in building an exciting, science-driven company. | 07/18/2024 |
| 2758 | Q2 Solutions Marietta, GA Associate Scientist, Flow Cytometry Bachelor’s Degree in a scientific field including chemistry, biology or medical laboratory technology. Exp: 6+ months |
In this vital role, you'll support daily laboratory functions, including inventory management, pre-analytical sample handling, and more, ensuring efficient and effective operations. What you’ll be doing: Performing and documenting analytical procedures, adhering to SOPs and regulatory guidelines, and upholding our laboratory's high-quality standards. Analyzing routine data, identifying deviations or unusual results, and reporting these findings promptly to senior lab personnel to safeguard our scientific work's integrity. Engaging in quality investigations, preparing necessary materials for analyses, and demonstrating your commitment to scientific accuracy and rigor. Mentoring entry-level staff, facilitating their onboarding, and participating in continuous education initiatives to strengthen our team's expertise foundation. Taking part in cross-functional projects, communicating effectively across various teams, and advocating for safety, quality, and adherence to organizational standards and initiatives. | 07/18/2024 |
| 2759 | Q2 Solutions Indianapolis, IN Associate Scientist, Biotransformation Bachelor’s degree in a relevant scientific discipline Exp: 6+ months |
We are seeking an Associate Scientist, Biotransformation to join Q2 Solutions, IQVIA’s laboratory business in Indianapolis, Indiana. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. What You’ll Be Doing: Perform routine analysis and laboratory testing procedures to obtain data from pre-clinical and/or clinical specimens. Document analytical procedures in accordance with methods and regulatory guidelines. Assess whether analytical procedures are proceeding according to expectations and ensure results are within acceptable tolerances. Identify abnormal progress, potential quality failures, or unusual results and escalate to senior lab personnel. Prepare data analysis results for upload to LIMS system under the guidance of senior-level staff. Assist in writing laboratory procedures and techniques. | 07/18/2024 |
| 2760 | Q2 Solutions Durham, NC Associate Scientist Bachelor’s Degree in a chemical, physical, biological, or clinical laboratory science, medical laboratory technology, or cytotechnology. Exp: 6+ months |
We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. The Associate Scientist will be instrumental in conducting and documenting analytical procedures, ensuring compliance with SOPs and regulatory guidelines, and contributing to the advancement of our laboratory operations. | 07/18/2024 |
| 2761 | Q2 Solutions Marietta, GA Laboratory Assistant, Inventory Control Bachelor’s Degree or equivalent combination of education Exp: 6+ months |
As a Laboratory Assistant, Inventory Control you will be providing lab support, necessary to assist the local inventory process. You will also be managing reagent inventory for the Flow and PBMC departments. | 07/18/2024 |
| 2762 | NJ Bio Princeton, NJ QC Scientist (I&II) BS, MS, or PhD degree in chemistry, biology, biochemistry, or related discipline Exp: 1+ years |
The primary role is to provide analytical support for GMP manufacturing and process development. The QC scientist will develop, qualify, and execute analytical test methods for raw materials, highly potent APIs, antibody-drug conjugates (ADCs), and other pharmaceutical products in a GMP setting. | 07/18/2024 |
| 2763 | Avecia Cincinnati, OH Associate Chemist BS degree in Chemistry or related areas Exp: 0+ years |
As an Associate Chemist, you will execute chemistry and related activities for manufacturing, packaging and shipping of OliGrow oligonucleotides according to company processes. | 07/18/2024 |
| 2764 | Noah Medical Sunnyvale, CA Clinical Engineer Bachelor’s degree in Engineering or Science; Master’s degree preferred Exp: 0-5 years |
The Clinical Engineering Team at Noah Medical is dedicated to ensuring the products Noah is developing meet all of the clinical and user needs. We collaborate closely with our end users (physicians) to understand their needs and the clinical value Noah’s products will bring them. The Clinical Engineering team also works closely with cross-functional development teams to represent clinical value propositions for patients and providers throughout the design and development of new products. Join us to contribute to Noah Medical's growth and to shape the future of medical robotics. | 07/18/2024 |
| 2765 | Noble Life Sciences Sykesville, MD Research Technician Bachelor’s degree in biological sciences, biomedical engineering, or a related field. Exp: 1+ years |
Job Description: Compliance: Perform assigned tasks and responsibilities under the direction of the Scientist(s) and/or the Study Director(s) and in accordance with relevant study protocols, regulations, and Standard Operating Procedures (SOPs); Training: Ensure personal training is documented according to Noble SOPs prior to the performance of associated procedures; Procedure Preparation: Label tubes and other supplies needed for collecting and processing specimens. Prepare reagents needed for collection or processing of specimens. Performance of Procedures: Process various blood and tissue samples. Maintain quality, safety, and/or infection control standards. Perform procedures using various instrumentation according to Noble SOPs; Documentation: Maintain lab notebooks and document experimental procedures and associated data. Assist in writing deviations and preparing responses to quality assurance audits related to duties performed. Laboratory Maintenance: Take ownership of assigned laboratories. | 07/18/2024 |
| 2766 | NorthStar Beloit, WI Radiopharmaceutical Manufacturing Associate Associate’s or Bachelor’s degree in a STEM discipline Exp: 0-1 years |
The Radiopharmaceutical Manufacturing Associate performs duties to support the development and manufacturing of radiopharmaceuticals for NorthStar operations. This includes equipment preparation, product dissolution, and dispensing of medical radioisotopes while complying with procedures, instructions, and prescribed routines. All duties and responsibilities will be completed in compliance with applicable regulatory agency standards. This position supports production in a 24-hour manufacturing facility which means your schedule provides days off during the week when weekend work is required. Early morning, late evening, weekend, and some holiday work will be required with occasional overtime. | 07/18/2024 |
| 2767 | NorthStar Beloit, WI Quality Control Analyst/Senior Quality Control Analyst Bachelor’s Degree in Chemistry, Biology, or other related scientific discipline Exp: 1+ years |
The primary role of this position is to conduct and validate various biological and analytical quality control assays associated with the processing of radiopharmaceutical isotopes and drugs to ensure compliance with established standards. This role requires extensive training on radiation safety including ALARA (“as low as reasonably achievable”) principles. Duties will be completed in compliance with applicable regulatory agency standards. This position supports production in a 24-hour manufacturing facility which means your schedule provides days off during the week when weekend work is required. Early morning, late evening, weekend, and some holiday work will be required with occasional overtime. | 07/18/2024 |
| 2768 | Machine Solutions Flag Staff, AZ Medical Device Testing Technician Bachelor’s level degree, preference for engineering or technical experience or Exp: 0+ years |
Machine Solutions testing equipment is used to evaluate and quantify the performance of our customers’ interventional devices such as stents, catheters, and guide wires. Testing/applications technicians are responsible for lab-based tasks, which include sample processing, contract testing, measuring, recording, analyzing results and generating reports on MSI equipment with in-house or customer product. The technician will learn how to operate Machine Solutions equipment and use this knowledge to host customer training and perform quality inspections to ensure equipment meets operational specifications. An ideal candidate will be someone who enjoys working with their hands and enjoys the challenge of finding unique solutions to meet our customer’s needs. | 07/01/2024 |
| 2769 | Macrogenics Rockville, MD Manufacturing Associate II - Cell Culture Bachelor’s degree in a related discipline and a minimum of three years of related biopharmaceutical manufacturing experience in FDA regulated, control Exp: 1+ years |
The Manufacturing Associate II participates in the manufacturing of biopharmaceutical drug product to support MacroGenics’ multiple clinical programs in the Protein Purification area. This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) to ensure that materials manufactured meet required specifications and regulatory requirements. | 07/01/2024 |
| 2770 | Macrogenics Rockville, MD Manufacturing Associate I - Cell Culture Bachelor’s degree in a related discipline Exp: No Experience |
The Manufacturing Associate I participates in the manufacturing of biopharmaceutical drug product to support MacroGenics’ multiple clinical programs in the Cell Culture area. This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) to ensure that materials manufactured meet required specifications and regulatory requirements. | 07/01/2024 |
| 2771 | MagBio Genomics Gaithersburg, MD Production and Fulfilment Associate Bachelor's Degree in Biology or equivalent science-related field; or equivalent combination of education and experience. Exp: 0-2+ years |
This position is responsible for the timely and efficient scheduling production, packaging and shipping of standard and custom products, and for providing support to other areas of manufacturing to ensure timely product delivery. Responsibilities with reagent production, shipping, and order fulfilment. | 07/01/2024 |
| 2772 | Magnolia Medical Technologies Seattle, WA Engineering Intern, Product Development (Hybrid) Pursuing an engineering degree, or related BA/BS degree, or pursuing a related MA/MS. Exp: Entry Level |
The Engineering Intern performs, under direct supervision, and contributes to the Engineering and Product Development Department of Magnolia Medical Technologies, Inc. The Intern is exposed to the medical device industry and Magnolia Medical's company culture through partnering with the organization’s teams, department supervisors and leaders who provide informal mentoring and coaching towards success. The Engineering Intern develops working knowledge of product development, works in a changing environment, and will further develop skills utilized industry wide in regulatory environments. | 07/01/2024 |
| 2773 | Mallinckrodt Pharmaceuticals St. Louis , MO Chemical Process Technician Minimum of a Bachelor's degree in Chemistry, Biology or other science degree. Exp: 1-3+ years |
Develop and produce pharmaceutical products via multiple methodologies, follow standard operating procedures, maintain compliance with Good Manufacturing Practices. | 07/01/2024 |
| 2774 | Mallinckrodt Pharmaceuticals Hobart, NY Quality Technician I - First Shift Bachelor Degree in science related field (Chemistry, Biology) is preferred Exp: I: Class/previous work exp in science related field II: Working knowledge of chemistry required III: Min 1-3 years of exp in cGMP facility |
Perform basic wet chemistry, preparation of reagents/solutions, and sample reconciliation following approved methods. | 07/01/2024 |
| 2775 | Mallinckrodt Pharmaceuticals Hobart, NY Validation Technician III Bachelor Degree in engineering discipline, life sciences or technical field related to pharmaceutical manufacturing is preferred Exp: 0-1 years |
Assists with multiple cross-functional projects from development through release for commercial implementation. Supports departmental priorities and senior level engineers with guidance from the department manager. May support the execution of validation studies as needed, including assisting in pre-run training, product sampling, and review of documentation for completeness and alignment with good documentation practices. Assists in the analysis and review of data generated by validation studies performed within the department. | 07/01/2024 |
| 2776 | Mallinckrodt Pharmaceuticals Hobart, NY Validation Engineer I Bachelor Degree in engineering discipline, life sciences or technical field related to pharmaceutical manufacturing is preferred Exp: 1-2 years |
Assists with multiple cross-functional projects from development through release to production. Projects include new facilities startup, manufacturing equipment and packaging line FATs and qualifications. Independently executes activities in support of the Validation Department priorities with minimal guidance from the department manager. Provides technical assistance during investigations of equipment/process/product issues. Supports validation deviations related to equipment/process/product. Execute validations as needed, including assisting in product sampling, auditing and technical review functions as defined in study protocols. Analyzes data, utilizing appropriate statistical methods, generated by validation studies performed by the Validation group to determine process capabilities. | 07/01/2024 |
| 2777 | Mallinckrodt Pharmaceuticals Madison, WI Quality Analyst Bachelor’s Degree Exp: 1+ years |
The Quality Analyst ensures that all materials, activities, processes, and specified conditions involved in daily device manufacturing, processing, and packaging meet current GMP standards and comply with relevant procedures and standards to maintain product quality integrity. Additionally, the Quality Analyst manages nonconforming material reports, plans material review board meetings, and oversees the status of quarantined and scrapped materials. | 07/01/2024 |
| 2778 | Mammoth Biosciences Mammoth Brisbane, CA Research Associate II/Senior Research Associate – LNP Formulation Bachelor's degree in chemistry, pharmaceutical sciences, bioengineering, chemical engineering, or related discipline with 1+ years of experience or Ma Exp: 0-1 years |
In this role, the successful candidate will be contributing to the formulation efforts of Mammoth’s proprietary CRISPR nuclease systems, supporting the formulation and physiochemical characterization of the candidates for a variety of therapeutic indications. In addition, this candidate will be contributing to the analytical method development to support the formulation discovery and production of test articles to support Mammoth’s ex-vivo and in vivo studies. | 07/01/2024 |
| 2779 | Mariana Oncology Watertown, MA GMP Manufacturing Technician Bachelor’s Degree, Associate Degree, or 5 years of experience working in a GMP manufacturing environment in the pharmaceutical or biotechnology indust Exp: 0-5 years |
Mariana Oncology is focused on an extremely exciting field of oncology of precision radiopharmaceuticals to treat unmet need in solid tumors. We are at the vanguard in developing best in class alpha and beta emitting radio ligands targeting cancer tumors while mitigating destruction to healthy tissue and cells. We have built a fully integrated, leading radiopharmaceutical platform, that is bringing together novel target biology insights, innovative multimodal ligand discovery, and enabling translational infrastructure. We are seeking an experienced GMP Manufacturing Technician to join Mariana’s Manufacturing organization, advancing personalized medicine and radiopharmaceuticals. | 07/01/2024 |
| 2780 | Mariana Oncology Watertown, MA Quality Control Analyst I/II Master’s degree in biochemistry, chemistry or related discipline with 0-2 years exp, or Bachelor's degree with 2-4 years exp Exp: 0-2 years |
We are seeking an experienced Quality Control Analyst I/II to join Mariana’s Clinical Manufacturing organization, advancing personalized medicine and radiopharmaceuticals. You will be responsible for supporting the release and stability testing of our clinical therapies produced in our GMP manufacturing suite in Watertown. This person will play a role in creating and maintaining the highest standard of excellence for our therapies to treat cancer patients. | 07/01/2024 |
| 2781 | Marvel Biome Woburn, MA Research Associate BS or MS in Molecular Biology, Microbiology, or Cell Biology required Exp: 0-2 years |
We are seeking a full-time Research Associate to join a highly collaborative team using the latest molecular biology, protein biochemistry, and -omics analysis techniques to develop microbiome-based therapies. In addition, there will be opportunities to assist in the execution of pre-clinical studies to evaluate treatment efficacy. The ideal candidate is obsessed with the question of how to best design and execute experiments to identify treatment-improving therapies. This is a unique opportunity to work at a nimble, forward-thinking microbiome start-up and help build the foundation for microbiome as therapeutics. | 07/01/2024 |
| 2782 | MatTek Ashland, MA Production Associate I Bachelor’s degree in biology or equivalent with no previous work experience Exp: 0+ years |
Participates in duties associated with manufacturing of MatTek tissue models according to SOPs where applicable. May also perform duties assigned under Laboratory Assistant, as needed. | 07/01/2024 |
| 2783 | Maze Therapeutics San Francisco, CA Research Associate, In Vivo Pharmacology Bachelors degree in biology, pharmacology, or other relevant field is required Exp: 1+ years |
Are you driven by a passion for scientific discovery and a desire to make a tangible impact on human health? We're seeking a passionate, creative, and dedicated Research Associate to join our in vivo pharmacology team. In this role, you will be pivotal in conducting pharmacokinetic studies that drive our research projects forward, while also contributing to preclinical pharmacodynamic and disease models. Under the guidance of the Director of Pharmacology, your work will directly support the discovery of new drug candidates and advance our understanding of disease mechanisms. Additionally, as a rapidly growing biotech company, we offer an exciting and collaborative work environment where every team member plays a vital role in our success. | 07/01/2024 |
| 2784 | Mdxhealth Irvine, CA Product Development Associate Bachelor's degree with 1-2 years of experience working in research & development or Master's degree with 0 to 3 years’ experience. Exp: 0-3 years |
The Product Development Associate is involved in assisting with the planning, conducting, and analyzing experiments leading to validation of diagnostic tests in the field of oncology. The PD Associate works in a team and needs to communicate relevant information to professional colleagues and to participate constructively in discussions that will impact the performance of the final product. | 07/01/2024 |
| 2785 | Mdxhealth Irvine, CA Inventory Control Associate High School Diploma or Bachelor's Degree Exp: 1-2+ years |
The function of an Inventory Control Associate is to keep track of the goods and supplies of the Operations teams, both incoming receipt and outgoing release to the laboratories. The Inventory Control Associate is to keep records of inventory counts, generate and place purchase orders, coordinate with vendors, maintain inventory of items in stock, and perform data entry of this information. The Inventory Control Associate is to monitor and handle purchases to ensure arrival in a timely fashion in the quantity and quality that upholds mdxhealth standards while maintaining supplier and interdepartmental relationships. | 07/01/2024 |
| 2786 | MedAbome Fremont, CA Research Associate (Molecular Biology) M.S. or B.S. degree in life science with academic or industrial experience in biological research Exp: 0+ years |
Perform molecular biology experiments to support drug discovery and development; Participate in antibody engineering, cell line generation, in vitro and in vivo assays. | 07/01/2024 |
| 2787 | MedAbome Fremont, CA Research Associate (Cell Biology) M.S. or B.S. degree in life science with academic or industrial experience in biological research Exp: 0+ years |
Maintain cell lines and perform cell-based assays to support antibody drug discovery; Participate in antibody generation and characterization, such as fusion, ELISA, FACS and other cell-based assays; Participate in small animal studies. | 07/02/2024 |
| 2788 | Medmix Flowery Branch, GA Technical Project Engineer Bachelor’s degree in mechanical or industrial engineering Exp: 1+ years |
We are looking for a Technical Project Engineer to join us at medmix. This exciting opportunity will allow you use your skills to identify areas of improvement and propose recommendations to management. You will lead and drive the implementation of your recommendations and assess its impact to the business. If you are eager to learn, strive for personal development, are highly motivated and organized, and a great communicator, you can help us drive medmix to the next level. As a Technical Project Engineer you will help us to take effective project management to the next level. Responsibilities: Realization of injection molding life cycle projects in the segments industry, dental and surgery, Lead interdisciplinary project teams, Create and update of project plans and necessary documents, Reach the goals set for cost, time and quality, Delegate and control tasks and execution of work packages within the projects, Execution of mile stone meetings | 07/02/2024 |
| 2789 | Medpace Cincinnati, OH Laboratory Technologist - Sample Processing Bachelor's degree in a Biological Science field or Chemical Science field Exp: 1+ years |
Our biorepository activities are growing rapidly, and we are looking to add to our sample processing team! The Laboratory Technologist will aid in the development and growth of the biorepository sample processing department. The ideal candidate will have strong critical thinking and problem solving abilities. This position will be a full-time, position in Cincinnati, OH. | 07/02/2024 |
| 2790 | Medpace Irving, TX Clinical Research Associate (CRA) Must have a minimum of a Bachelor’s degree in a health or science related field Exp: 0+ years |
The Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with a medical and/or health/life science background who want to explore the research field, travel the US, and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you! | 07/02/2024 |
| 2791 | Medpace Cincinnati, OH Chemistry Laboratory Technician A minimum of a Bachelor's degree, with previous experience in a research laboratory Exp: 1+ years |
Responsibilities: Prepare samples according to project protocol and/or related SOPs; Maintain compliant laboratory documentation; Perform data analysis and data checking; Interpret results obtained for accuracy and acceptability; Clean and sterilize laboratory equipment; and Other duties deemed necessary. | 07/02/2024 |
| 2792 | Medpace Cincinnati, OH Laboratory Quality Assurance (QA) Auditor Bachelor’s degree in the science or a related field Exp: 1-3 years |
The QA Auditor role will be responsible for both internal and external audits, as well as coordinating, conducting, and tracking company-wide Regulatory Training, CAPA Investigations and Metric Analysis. This role will also ensure Compliance to Standard Operating Procedures (SOPs), current Regulations, and Standards. In addition, the Auditor will assist in the creation and maintenance of Controlled Documents. This role is highly visible to Medpace Internal and External Clients; therefore, this role requires excellent Communication Skills, a Proactive Enthusiasm, and Critical Thinking. | 07/02/2024 |
| 2793 | Medpace Cincinnati, OH Laboratory Technologist Bachelor's degree in a Biological Science field or Chemical Science field Exp: 0+ years |
The Laboratory Technologist at Medpace Reference Laboratories plays a pivotal role in research based drug development within the pharmaceutical industry. Due to our recent growth, we are in need of qualified and focused driven individuals, like yourself! You would have the unique opportunity to work on the laboratory side of the fast paced medical world by conducting routine and esoteric testing on blood, tissue, and body fluids. If you have an analytical mind set, and enjoy working in a team-oriented laboratory setting, this could be the opportunity for you! | 07/02/2024 |
| 2794 | MedPharm Durham, NC Associate Scientist-Performance Testing Bachelors degree, education may be used in lieu of experience Exp: 0-2 years |
The Associate Scientist is an essential member of the laboratory team. They work with the Performance Testing team to conduct in vitro permeation and release testing for topical and transdermal formulations. They also conduct analysis of research projects and results and help develop nonstandard tests. Associate Scientists have the opportunity to collaborate with fellow scientists in study planning, formulation development, analytical, and tissue culture. We are looking for an eager individual who wants to develop personally and professionally. You should have a strong attention to detail, be a go-getter, and be continuously striving for self-improvement. You are passionate about good science and want to help out in any way possible. We are looking to invest in someone who wants to grow not only in this role but also in their scientific career. | 07/02/2024 |
| 2795 | Medtronic Fridley, MN Hardware Engineer I Bachelors degree in Electrical Engineering, Computer Engineering or related field required Exp: No Experience |
This position will provide Electrical Design and System Test support for the Translational Research System team on Neuromodulation & Pelvic Health Implantable products such as cutting-edge neurostimulator systems for Deep Brain Stimulation, Spinal Cord Stimulation, and Sacral Nerve Modulation. The individual will support all phases of development including definition, design, troubleshooting, characterization, and verification of medical device research systems. The individual will be an integral part of the R&T organization delivering the highest quality, life changing technology to our patients. This role requires a strong background in hardware development and testing, system integration and testing, and a passion for improving healthcare through technology. | 07/02/2024 |
| 2796 | Medtronic Danvers, MA Process Engineer I Bachelors Degree in a related engineering discipline (i.e., mechanical, biomedical, industrial, materials science) Exp: No Experience |
As a Process Engineer I, you will be involved with process development, setting up manufacturing operations, and interfacing cross-functionally with other key engineering expertise to develop a product. In this role, you will part of a team but will be able to work independently to determine and develop approaches to solutions. You will communicate with internal and external customers and suppliers. Your work will involve collaboration and dynamic interactions with R&D and Design Assurance regarding products in the development pipeline and with operation team members for new or iterative product implementation. | 07/02/2024 |
| 2797 | Medtronic North Haven, CT Manufacturing Engineer I Bachelors degree, preferred in Engineer Exp: No Experience |
The Manufacturing Engineer will be working with highly motivated team members and dynamic work environment. This is a great opportunity to interact and work with broad cross-functional groups including different manufacturing sites engineering, quality, share-services, marketing team and extensive business platforms, and suppliers to continuously improve the manufacturability. | 07/02/2024 |
| 2798 | Meissner Camarillo, CA Quality Assurance Coordinator Bachelor’s Degree from a 4-year accredited college or university Exp: 1-3 years |
As part of the Quality Assurance team, you will work closely with Quality Control, Customers, Engineering, Manufacturing, Sales and Marketing teams to ensure that solutions in development and in production meet the needs of our customer base and are compatible with the regulatory environment of our industry. As part of the Quality Assurance team, you will work closely with Quality Control, Customers, Engineering, Manufacturing, Sales and Marketing teams to develop and improve our Quality Management System (QMS). Work collaboratively with the team to develop, implement, maintain and ensure the performance of the company’s QMS. Utilizing leading-edge technology, you will support customer inquiries by monitoring Meissner’s Quality inbox, coordinating responses and assigning inquiries to the appropriate parties. Support and ensure compliance with established company policies and procedures, objectives, quality assurance program. Support implementation of QA procedures and documents. Review SOPs to ensure alignment with quality guidelines and documents. | 07/02/2024 |
| 2799 | Meissner Camarillo, CA R&D Scientist I Bachelor’s degree required in STEM-related field Exp: 1-5 years |
Are you a passionate scientist ready to push the boundaries of research and development? Join our dynamic R&D team as an R&D Scientist I, where you’ll spearhead groundbreaking experiments, analyze cutting-edge data, and contribute to revolutionary product advancements. If you thrive in a collaborative environment and are driven by discovery, we want you on our team! Our customers use our products and technologies to develop new therapeutics and many familiar products that support our modern lifestyle. At the core of these products, are in-house technologies that are developed and maintained by highly talented and self-driven engineers and scientists. Participate in technology development projects, Assist in technology transfer of R&D Activities to manufacturing, Support our technologies to continuously improve our products and processes. | 07/02/2024 |
| 2800 | Teva Pharmaceuticals Salt Lake City, UT Quality Control Analyst I Bachelor’s degree, preferably in the sciences or any combination of equivalent education Exp: 0+ years |
Teva has an opportunity for a passionate Chemist to join our team. As a key part of our dedicated, friendly, and collaborative Product Quality Team, you’ll play an essential role in laboratory testing of pharmaceutical product in support of commercial product release. This role is great role to learn the pharmaceutical manufacturing process. Many of our entry level lab analysts advance into other roles in Science, Quality and Production. | 07/02/2024 |
| 2801 | Mercury Bio Santa Fe, NM Research Associate BS or MSc in related fields and previous research experience Exp: 1+ years |
Mercury Bio has immediate openings for Research Associates with expertise in molecular genetics, biochemistry, bioinformatics, immunology and microbial or human cell culture. Ideal candidates should have a BS or MSc in related fields and previous research experience. This position requires creative and critical thinking, as well as the ability to work independently. Mercury Bio is located in Santa Fe, NM and focuses on the development of RNA therapeutics to control gene expression in humans in a safe and dose-dependent manner. | 07/02/2024 |
| 2802 | Meridian Bioscience Memphis, TN Quality Assurance Associate Bachelor’s degree from accredited institution in life science, chemistry, pharmaceutical science, statistics, or health/human services related field. Exp: 0-5 years |
The Quality Assurance (QA) Associate will support QA processes, programs, and conduct QA activities. This position will uphold standards, methods, and procedures for all stages of production. This position will identify continuous process improvement areas, in compliance with Good Manufacturing Practices (GMP) and Good Documentation Practices (GLP) processes and documentation for quality control activities. This requires excellent technical skills and abilities, analytical and mathematical skills, organizational and time-management skills, verbal, and written communication skills, plus ability to apply attention to detail. | 07/02/2024 |
| 2803 | Meridian Bioscience Memphis, TN Quality Control Analyst Bachelor's degree in a scientific discipline or equivalent Exp: 1 years |
The Quality Control Analyst position performs testing and inspection of raw materials, in-process and finished products, and audits the corresponding documentation in compliance with internal SOPs and applicable regulatory requirements, participates in test method validation development and execution, and assists in the training and development of new Quality Control Analysts. The Quality Control Analyst is also responsible for performing duties required in the application and continued improvement of the company’s Quality System. | 07/02/2024 |
| 2804 | Meridian Bioscience North Billerica, MA Research Associate Bachelor of Science degree required, experience with analytical chemistry strongly preferred Exp: 0+ years |
Primary role is to run experiments, acquire and record data.Tasks/Duties/Responsibilities: Support projects by conducting experiments, acquiring, and accurately documenting data. Contribute to completion of milestones associated with specific projects. Expected to grow and develop in this role and be able to draw conclusion from studies and design experiments. | 07/02/2024 |
| 2805 | Meridian Bioscience Memphis, TN Lab Production Associate (Antigens and Cell Culture) Bachelor’s or Master’s degree from an accredited institution with a relevant scientific discipline such as Chemistry, Biology, Biochemistry, Molecular Exp: 0+ years |
The Lab Production Associate position is responsible for performing assigned manufacturing and laboratory support activities according to company policies, SOPs, and quality regulations. The position will be responsible for performing upstream and downstream bioprocessing procedures to support the commercial manufacturing of native antigens, recombinant proteins, antibodies, and blockers. Upstream processes include tissue culture, cell bioreactors, fermentation, virus propagation, cell and virus bank production, and buffer/media preparation. Downstream unit operations include harvest, clarification, chromatography, centrifugation, TFF (UF/DF), filtration, formulation, and fill-finish. The candidate will be required to maintain an assigned lab area and perform equipment and lab cleaning procedures. The candidate must be able to execute assigned procedures in a fast-paced and results-oriented environment satisfying quality standards in accordance with customer satisfaction, cost, schedule, and ISO1345 regulations. | 07/02/2024 |
| 2806 | Merit Medical South Jordan, UT Mfg Engineer I Bachelor’s or Master's Degree in Engineering Exp: 0+ years |
Performs routine technical work such as the design, manufacture and operation of structures, machines and systems under general supervision and guidelines. Performs routine technical work requiring the application of standard techniques, procedures, and criteria in carrying out engineering tasks. Uses limited amounts of discretionary judgment in making decisions regarding technical alternatives. Performs work of some higher technical level for training purposes, and work is screened to ensure correct application of scientific principles. Works on special projects, writes ECN's, and may create prototypes under general direction. Performs other related duties and tasks as required. | 07/02/2024 |
| 2807 | Merit Medical South Jordan, UT R&D Engineer II - (Endovascular) Part-time Bachelor’s Degree in Engineering or technical field related to the department of assignment Exp: 0+ years |
Performs routine and complex technical work such as the design, manufacture and operation of structures, machines and systems under broad supervision and guidelines. This position is 20 hours a week in the RND Endovasular division of Merit Medical. | 07/02/2024 |
| 2808 | Merit Medical South Jordan, UT Engineer II (Annual) Performs routine and complex technical work such as the design, manufacture and operation of structures, machines and systems under broad supervision Exp: 0+ years |
Performs routine and complex technical work such as the design, manufacture and operation of structures, machines and systems under broad supervision and guidelines. | 07/02/2024 |
| 2809 | Merit Medical South Jordan, UT Technician III Bachelor's Degree with 1 year of exp, Associate's Degree with 3 years of 3 years tech exp, or High school Diploma with 5 years of tech exp Exp: 1+ years |
Performs non-routine technical assignments of substantial variety and complexity. Performs assignments and may assist in planning assignments of a non-routine nature for which operational precedents are not fully applicable. Prepares test specimens, adjusts and operates equipment, and records test data, pointing out deviations resulting from equipment malfunction or observational errors. Extracts engineering or other data from various reports, processes the data, and presents the data. Receives technical advice from engineers or supervisor for complex problems. Working overtime may be required for this position. Performs other duties and tasks as required. | 07/02/2024 |
| 2810 | Meso Scale Diagnostics Gaithersburg, MD Scientist I, Bioanalytical Lab Bachelor's degree in life sciences, protein sciences, cellular/molecular biology, chemistry, biochemistry, biotechnology, or other related area is req Exp: 1+ years |
The Bioanalytical Scientist I provides supervision of daily laboratory operations, offers guidance, leadership and direction to lab personnel to ensure on-time completion of customer projects. This includes leading initiatives for the transfer of newly developed assays that have been developed for customers to the company's Bioanalytical Lab, supporting new instrumentation intended for use in sample testing services and managing studies performed in accordance with relevant regulations. This position will directly supervise the work of others in their group and/or across interdisciplinary teams. The Bioanalytical Scientist I will lead and/or direct the work of others, to include establishing the scope of work assignments, experiments and work schedules/deadlines. They are expected to independently manage multiple projects yielding high quality results, and provide oversight and guidance to other team members as needed. | 07/02/2024 |
| 2811 | Meso Scale Diagnostics Rockville, MD Quality Control Analyst I Bachelor’s degree in relevant field preferred. Associate’s degree in relevant field required. Exp: 0+ years |
Under general supervision, the Quality Analyst I performs routine quality control inspection, testing and data analysis for various incoming, in-process, and final products within MSD’s protein-based immunoassay catalog. This position will execute various laboratory cleaning activities to help support overall operations of Quality/Product Control. | 07/02/2024 |
| 2812 | Meso Scale Diagnostics Gaithersburg, MD Bioanalytical Associate I Bachelor’s degree in life sciences, protein sciences, cellular/molecular biology, chemistry, biochemistry, biotechnology, or other related area is req Exp: 0-2 years |
A Bioanalytical Associate I is responsible for handling biological samples, reagents, and materials in support of sample testing and assay service projects. This is a laboratory based position whose primary function will be sample management and handling, under direct supervision and direction. The incumbent may also perform protein-based immunoassays on a routine basis with relatively high throughput (2-8 plates per day). The incumbent is expected to adhere to all standard operating procedures and policies established for execution of Bioanalytical studies and sample testing projects under applicable regulatory compliance requirements. | 07/02/2024 |
| 2813 | Meso Scale Diagnostics Gaithersburg, MD Engineer I, Mechanical Bachelor’s degree in Mechanical Engineering Exp: 0+ years |
The Mechanical Engineer I is responsible for mechanical design, testing, and documentation of new instrumentation and support of exisiting instrumentation for the biodefense, clinical and life-science markets. Design work will include the design of precision mechanisms and complex assemblies that include machined, molded and sheet-metal components. | 07/02/2024 |
| 2814 | Meso Scale Diagnostics Gaithersburg, MD Engineer I, Automation Bachelor’s degree in Computer Science or Electrical, Mechanical, or Systems Engineering is required Exp: 0-1+ years |
The Automation Engineer I will design and build high performance, automated process equipment used for manufacturing and/or laboratory automation systems. These systems include, but are not limited to automated reagent dispensers, assembly, machine vision, and liquid handling systems for micro-plate test kit and micro-fluidic assay cartridges used in the biodefense, clinical, and life-science markets. | 07/02/2024 |
| 2815 | Meso Scale Diagnostics Rockville, MD Production Control Technician I Bachelor’s degree in life sciences, protein sciences, cellular/molecular biology, chemistry, biochemistry, biotechnology, engineering or a related fie Exp: 0-1+ years |
The Production Control Technician I is responsible for assisting in the control of production, documentation and inventory maintenance for multiple groups within Consumable Operations. | 07/02/2024 |
| 2816 | Meso Scale Diagnostics Gaithersburg, MD Engineer I, Systems Bachelor’s degree in Systems, Mechanical, or Electrical Engineering or a closely related field Exp: 0-1+ years |
The Systems Engineer I is responsible for assisting in the development and management of requirements and specifications, system integration and testing of electromechanical, fluidic, thermal control, and imaging systems, and formal verification and validation testing. | 07/02/2024 |
| 2817 | MethodSense Morrisville, NC Quality and Safety Engineer Bachelor’s degree in biomedical engineering or alternative engineering degree. Exp: 1-7 years |
We are looking for talented Quality and Safety Engineers to join our experienced team. If you can commit yourself to supporting a passionate regulatory affairs and quality assurance business dedicated to their clients, you can have a career with us. We need someone with honesty, integrity and excellent communication and interpersonal skills. The position requires the ability to work with client company executives, test labs and FDA regulators. It also requires agility and love for knowledge. If you want to join a high energy purposed team, please apply. | 07/02/2024 |
| 2818 | Metrohm Charlotte, NC Field Service Technician - Lab Equipment A degree or certification in Chemistry (or related STEM field) is preferred. Exp: 0+ years |
Field Service Technicians provide on-site preventative maintenance and basic service for Metrohm laboratory instruments. You will attend training classes at our headquarters in Tampa, FL. Field Service Technicians get to travel to a diverse group of labs, meet different people and see various instrument applications at work. You will have the resources to support the client face to face, via phone, email and Microsoft Teams. This is a remote position that requires some overnight travel in the NC/SC region. | 07/02/2024 |
| 2819 | MicroAire Surgical Instruments Charlottesville, VA Design Verification Engineer (Test Development) Bachelor’s in Mechanical or Biomedical Engineering required. Exp: 0+ years, internship exp applies |
Develops Plans for the Appropriate Verification and Validation (testing) of new products, line extensions, and product redesigns. | 07/02/2024 |
| 2820 | MicroVention Aliso Viejo, CA Engineer I, R&D Bachelor’s degree in Engineering or Scientific field. Exp: 6 months |
Support development of medical device products with work including writing or verifying specifications; designing new products and fixtures; testing processes and equipment; and specifying raw materials to ensure the concepts and/or prototypes meet their requirements. Job duties: Develop new product concepts and products. Provide engineering design and process development.Generate intellectual property; write invention disclosures. Supervise assemblers, technicians, and specialists. Partially self-directed and capable of meeting project goals with supervision. Some travel required. Perform additional responsibilities as assigned. | 07/02/2024 |
| 2821 | Mikart Inc Atlanta, GA Quality Control Analyst Bachelor of Science in Chemistry with 0 yrs exp or Bachelor of Science degree in a related science plus 1 year of applicable exp Exp: 0-1 years |
The Quality Control Analyst for Mikart, LLC is responsible for conducting analyses on various components, in process materials and finished dosage forms. Document all analyses performed through the use of notebooks and official forms. Immediately report any anomalies to the Team Leader. Enter data into spreadsheet templates and verify accuracy by performing minimal manual calculations. Assure the accuracy of all data used for batch calculations. Conduct all operations in strict accordance with applicable regulations, guidance documents, SOPs and Mikart policies and procedures, including computer data acquisition and integrity policies. Assure that all laboratory areas and workspaces are maintained in a neat and orderly fashion. Perform necessary cleaning, maintenance, and calibration of instrumentation, as required. Maintain or request appropriate supplies and materials necessary to complete all assignments. Assist in maintaining accurate documentation of all supplies and chemicals received and used. Maintain appropriate records of waste storage and disposal in accordance with Mikart procedures and appropriate regulations. Assure that laboratory reagents, solutions, standards, samples, and controlled substances are used and stored properly and in accordance with all applicable regulations and guidelines. Secure all assigned samples while testing is in progress. Assure all materials used in analyses are within their established expiry period. | 07/02/2024 |
| 2822 | Mikart Inc Atlanta, GA Quality Control Analyst (Microbiologist) Bachelor of Science in Biology with 0 yrs exp or B.S. degree in a related science plus one-year applicable experience, or other appropriate combinatio Exp: 0-1 years |
The Quality Control Analyst (Microbiologist) for Mikart, LLC is responsible performing analyses on incoming samples requiring microbiological testing. Receive incoming samples, including water, environmental, raw material and dosage form samples, and insure that information is accurately and promptly entered into logs. Perform microbiological or other testing required on incoming samples safely and in accordance with all GMP, USP and Mikart specifications and procedures. Document all analyses performed through the use of notebooks and official forms. Immediately report any anomalies to the supervisor. Report any discrepant, suspect or out-of-specification results to the Microbiology Supervisor immediately. Accurately follow investigation plan directives issued by supervisory personnel. Assure proper handling of materials under test, including controlled substances, and ensure proper storage of all samples. Assure that all waste is processed according to procedures before disposal. Complete usage and maintenance logs accurately and promptly for instruments and equipment present in the micro lab. Receive and assure that all laboratory reagents, solutions, standards, samples, and controlled substances are used, stored properly and in accordance with all regulations and guidelines. Secure all assigned samples while testing is in progress. Assure all materials used are within their established expiry period. Verify that all laboratory equipment is within the active calibration period. | 07/02/2024 |
| 2823 | Miltenyi Biotec Boston, MA Clinical Trial Associate Bachelor's Degree Exp: 0-2 years |
The Clinical Trial Associate (CTA) will support the clinical trial team, ensuring that all essential documentation is collected, maintained and filed during the study. Collaborate with Clinical Trial Manager(s) to assist in the operational and logistical aspects of clinical trial management tasks (e.g. start-up, maintenance, and close-out activities) according to ICH-GCP and standard operating procedures. Liaise with CROs and other clinical vendors to ensure deliverables are met and communication is efficient. Partner with Investigators and clinical site staff to ensure optimal Sponsor-Site relationships. Assist in the management of study to ensure adherence to timelines and achievement of study goals while ensuring high quality. | 07/02/2024 |
| 2824 | Mission Bio South SF, CA Sr Bioinformatics Scientist, Remote Master's or PhD degree in Computational Biology, Bioinformatics Exp: Relevant grad/postdoc experience are also welcome |
We are seeking a talented and motivated Computational Biologist/Bioinformatics Specialist to join our team. This role will be pivotal in supporting our pharma accounts, driving product development and clinical traction by utilizing advanced data analysis techniques, algorithm development, and effective communication with customers. The ideal candidate will have a strong background in data analysis, with a focus on single-cell analysis, and possess the skills necessary to refine algorithms for production environments and ensure compliance with regulatory standards. | 07/02/2024 |
| 2825 | Moderna Norwood, MA Engineer I, Process Engineering Bachelor’s degree in chemical engineering, mechanical engineering, or related field. Exp: 0-2 years |
In this role, you will support the operability and reliability of GMP manufacturing process equipment at Moderna's manufacturing facility in Norwood, MA. This individual will assist Facilities and equipment End Users with routine troubleshooting and optimization of process equipment. Applicants should enjoy working in a fast-paced, dynamic, and innovative environment. | 07/02/2024 |
| 2826 | MP Biomedicals Solon, OH Production Chemist Bachelor of Science in Chemistry, Biochemistry, or Biology or equivalent work/school experience. Exp: 0-3 years |
The production chemist will be trained on two different product lines. This position will rotate training through two manufacturing areas that include Immunology and Molecular Biology Liquids. Learn and be responsible for a wide variety of product formulation tasks. Follow and optimize production processes while following safety protocols. Produce quality research products in a timely fashion to meet customer demand. Responsibilities will include: Operation of lab equipment including spectrophotometer, plate reader, centrifuges, pipettors, etc., Purification of antibodies from whole antisera using affinity chromatography methods. Conjugation of antibody to enzymes/fluorochromes. Maintenance of detailed records of products in production. Perform Quality Control testing for Immunology products (UV-VIS, Immunoelectrophoresis, and ELISA). | 07/02/2024 |
| 2827 | Myriad Genetics Salt Lake City, UT Research Associate (Onsite) BA/BS or MS in Molecular Biology, Cell Biology, Genetics, Biochemistry, Biophysics, Chemistry, or a related discipline Exp: 1+ years |
We are looking for a Research Associate to join our interdisciplinary R&D team that includes scientists in Salt Lake City and South San Francisco (this posting is for a role in Utah). The ideal candidate will have hands-on experience with a range of current molecular biology techniques, with particular focus on NGS. We are seeking a collegial teammate who is curious and rigorous, an individual who shares our enthusiasm for improving people’s lives by building the products that power precision medicine. | 07/02/2024 |
| 2828 | AlloyTx Waltham, MA Research Associate, Antibody Discovery B.S. in Immunology, Molecular Biology, or related discipline. Exp: 0-2 years |
As a Research Associate, Antibody Discovery, you will work with our ADS team to build new antibody technologies for the discovery of antibody-based therapeutics. You will be using the very latest single-cell techniques with the goal of identifying drug candidates in close collaboration with our partners. This role requires strong molecular biology skills, and the ability to plan and execute lab activities efficiently. This role will report to Head of In-Vivo Antibody Discovery with autonomy owning various stakeholders, projects, and tasks in a dynamic start-up environment while keeping up the pace of Alloy. This is you! | 5/17/2024 |
| 2829 | AlStem Bio Richmond, CA Research Associate B.S. or M.S. degree in Biochemistry, Molecular Biology or related discipline. Exp: 1 year |
ALSTEM, INC is a growing research biotechnology company located in Richmond, CA. ALSTEM is a nimble provider of tools specializing in virus packaging, genome editing, cell engineering and stem cells for life science research. ALSTEM is looking for a highly organized and energetic Research Associate with a B.S or M.S. degree to join its scientific team. The candidate will be responsible to work as a team at all levels which will include but will not be limited to product testing and QC, and custom service projects following SOPs and protocols to support customer workflows. | 5/17/2024 |
| 2830 | Alta Sciences Columbia, MO Associate Scientist, DCA M.S. Exp: +1year |
In the performance of their respective tasks and duties, the Associate Scientist, Dose Concentration Analysis are expected to be engaged in the conduct of or responsible for the supervision of a nonclinical laboratory study shall have the education,training and experience, or combination thereof, to enable that individual to perform their assigned functions. They will also need to comply with Good Laboratory Practices (GLP), and all regulatory requirements applicable to the position. They will need to develop, revise, review and implement Standard Operating Procedures {SOPs) as applicable to the position. The Associate Scientist will need to understand and incorporate the information contained in the Employee Handbook into day to-day job performance and strive to demonstrate the Company's values in all work-related activities. They'll need to provide technical and scientific leadership in the area of analytical chemistry. This role requires them to plan and execute projects, identify and acquire the necessary facilities equipment and procedures for research projects by performing the below duties. | 5/17/2024 |
| 2831 | Alta Sciences Everett, WA Research Associate - Flow Cytometry Associate degree in scientific discipline. Exp: 6 months |
As a Research Associate I, you will be at the forefront of groundbreaking research, contributing to the success of our laboratory through diverse responsibilities that go beyond the ordinary. Engage in hands-on activities such as equipment maintenance, supply stocking, and general cleaning while supporting our Flow Cytometry team. | 5/17/2024 |
| 2832 | Alta Sciences Everett, WA Research Associate II - Biomarker Associate degree in scientific discipline. Exp: 6 months |
As a Research Associate II, you will be at the forefront of groundbreaking research, contributing to the success of our laboratory through diverse responsibilities that go beyond the ordinary. Engage in hands-on activities such as equipment maintenance, supply stocking, and general cleaning while supporting our Biomarker assay team. | 5/17/2024 |
| 2833 | Alta Sciences Scranton, PA Research Associate - Laboratory Animals BS/BA in a scientific discipline preferred. Exp: 0-2 years |
Do you love working with animals? Do you want to contribute to advancing human health science research? Do you like to work in small teams? Altasciences is seeking Research Associates at all levels of experience that have a passion for scientific research. In this position your focus will be working directly with animals in the collection of data and in support of the development of human medicine. You will perform technical procedures to support advancements in pharmaceutical development. In this position you will learn and perfect complex procedures including learning the skills to operate laboratory equipment, specimens collection techniques and data acquisition. At Altasciences Preclinical Services, we work with many different animal models: mice, rats, non-human primates, swine and canine and you will have the opportunity to become a proficient, highly skilled expert in this field. Multiple shifts available. | 5/17/2024 |
| 2834 | Alta Sciences Everett, WA Research Associate PCR - Laboratory Sciences Associate degree in scientific discipline. Exp: 6 months |
As a Research Associate III, you will be at the forefront of groundbreaking research, contributing to the success of our laboratory through diverse responsibilities that go beyond the ordinary. Engage in hands-on activities such as equipment maintenance, supply stocking, and general cleaning while supporting and executing data collection activities involving qPCR, ddPCR, and DNA isolation, . | 5/17/2024 |
| 2835 | Alta Sciences Columbia, MO Research Associate II, Laboratory Sciences Associates/Bachelor’s degree in Immunology/ Biology/ Chemistry or equivalent scientific discipline. Exp: 1-3 years |
The Research Associate II, Laboratory Sciences role works independently in the day-to-day laboratory operation, collection, and review of data for the Laboratory Sciences department. Support and perform data collection activities including ligand binding assays, and/or flow cytometry, and/or cell-based assays, and/or mass-spectrometry, and/or as assigned. Participates in the creation of study worksheets, SOPs and other documents as assigned. Provides support for general laboratory equipment and maintenance as assigned. | 5/17/2024 |
| 2836 | Alta Sciences Everett, WA Research Associate I - Small Animal Unit BS/BA in a scientific discipline preferred. Exp: 0-2 years |
Do you love working with animals? Do you want to contribute to advancing human health science research? Do you like to work in small teams? Altasciences is seeking Research Associates at all levels of experience that have a passion for scientific research. In this position your focus will be working directly with animals in the collection of data and in support of the development of human medicine. You will perform technical procedures to support advancements in pharmaceutical development. In this position you will learn and perfect complex procedures including learning the skills to operate laboratory equipment, specimens collection techniques and data acquisition. At Altasciences Preclinical Services, we work with many different animal models: mice, rats, non-human primates, swine and canine and you will have the opportunity to become a proficient, highly skilled expert in this field. Multiple shifts available. | 5/17/2024 |
| 2837 | Aluna Alameda, CA Scientist I - Research and Development BA/BS degree in Biochemistry, Molecular Biology, Microbiology or related field. Exp: 1-3 years |
Alveo Technologies is looking for a Research and Development Scientist 1 to support R&D efforts of projects in disease detection. A successful candidate will assist in planning and executing protocols, and conducting experiments at the bench to meet objectives. The candidate should be able to review, understand and follow the instructions, protocols and SOPs provided by R&D. | 5/17/2024 |
| 2838 | Alvogen Norwich, NY Quality Systems Specialist I Level I: Associate or Bachelor of Science in Chemistry, Life Science, Engineering or combination of training, education, and experience that is equiva Exp: 1 - 3 years |
The Quality Systems Specialist provides system administration and support of daily quality activities to ensure compliance with global regulatory requirements and guidelines (FDA, ICH, EU, WHO, etc.). | 5/17/2024 |
| 2839 | Alvogen Norwich, NY Chemist I BS in Chemistry, Biochemistry, Microbiology or Biology or related discipline. Exp: 0-3 years |
The Quality Control Chemist I / Microbiologist I: Performs routine testing to assess the conformance of raw materials, finished products, and/or stability samples to predetermined product specifications. Performs routine testing in conformance with approved procedures, accurately and concisely documents data, and reports results. Demonstrates a basic knowledge of SOP’s and GMP regulations as related to the pharmaceutical quality control laboratory. | 5/17/2024 |
| 2840 | Amber Bio San Francisco, CA Research Associate Bachelor’s or Master’s degree in Biology, Biochemistry, Chemical Engineering, Biological Engineering, or a related field. Exp: 1 year |
Responsibilities: ● Work in a highly collaborative team focused on advancing our gene editing platforms. ● Support technology development strategy and design/build/test improved systems. ● Support engineering and characterization of editing systems with high-throughput experimentation. ● Maintain detailed, well-organized, and timely documentation of experiments and data. ● Effectively analyze and present data, and communicate research plans and timelines to the core team. ● Live Amber Bio’s core values of being biologically inspired, being honest and rigorous about our research, and fostering a supportive environment. | 5/17/2024 |
| 2841 | Amplify Bio West Jefferson, OH Asst./Associate Scientist, Analytical Sciences Bachelor’s degree in molecular biology, Biochemistry, Immunology, Molecular Genetics, or related field. Exp: 1 year |
AmplifyBio is currently seeking to hire an Assistant/Associate Scientist to join our growing Analytical Sciences team! The Assistant/Associate Scientist is responsible for performing analytical testing using a variety of cellular and/or molecular biology analysis platforms. Level of position and title will be based on experience and will report to a supervisor or senior scientist of Analytical Sciences. | 5/17/2024 |
| 2842 | ANI Pharmaceuticals Baudette, MN Quality Assurance Specialist Bachelors degree is required. Chemistry, medical technology, microbiology preferred. Exp: 1-2 years |
This position is responsible for providing support to the Manufacturing and Packaging Operations to ensure relevant procedures are followed and meet GMP requirements. This includes, but is not limited to the following: 2nd Shift Monday -Friday 3:15 pm to 11:15 pm | 5/17/2024 |
| 2843 | ANI Pharmaceuticals Baudette, MN Quality Control Chemist Bachelors degree in chemistry, biochemistry, microbiology or closely related field/major. Exp: QC Chemist – 1-3 years experience |
The QC Chemist position is responsible for independently performing testing in a pharmaceutical Quality Control laboratory. All work will be conducted in accordance with standard operating procedures and test methods. This includes performing testing on raw material, in-process and finished product samples. Execute compendia method validations, method transfers and validation support of new product development. Set up and confirm suitable operation of equipment and instrumentation. Collect data and generate/report results in accordance with governing test methods and SOPs. | 5/17/2024 |
| 2844 | Aphena Pharma Easton, MD Manufacturing Engineer BSME or equivalent experience. Exp: 1+ years |
Aphena Pharma Solutions is looking for a Manufacturing Engineer to join our team in Easton, MD! Aphena Pharma Solutions is a dynamic pharma solutions provider focused on contract packaging, repackaging and manufacturing for the pharmaceutical, OTC, dietary supplement, animal health and medical device marketplaces. | 5/17/2024 |
| 2845 | Appia Bio Culver City, CA Research Associate I/II MS in Biology or related major. Exp: 0-4 years |
We are seeking a creative and driven Research Associate I/II ready to take on the challenge and opportunity presented by the frontiers of creating novel engineered cell therapies. The individual will be part of the Molecular Biology team and support the efforts to generate and deliver critical gene expression plasmids and lentivirus preparations. The individual will primarily be working directly with an Appia Bio Scientist and will be required to work both independently and as a team in a fast-paced environment to support ongoing discovery projects. The Research Associate I/II will join a culture of intellectual rigor and collegiality that has been built at Appia. | 5/17/2024 |
| 2846 | Applied Medical Rancho Santa Margarita, CA Plastics Process Engineer II Bachelor’s degree in Polymer, Materials, Plastics, or Manufacturing Engineering (or equivalent). Exp: 1-2 years |
Collaboration is a fundamental part of our organization's culture and is essential to our continued success. As such, the successful candidate for this position is expected to work on-site, enabling them to engage fully with colleagues and contribute to cross-functional initiatives. Therefore, the ability to work collaboratively and contribute to a positive and supportive team environment is a key requirement for this role. As a Plastics Process Engineer II, you will use skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. | 5/17/2024 |
| 2847 | Aptitude Medical Santa Barbara, CA Research Associate Bachelor’s degree or Master’s degree in a relevant discipline. Exp: Entry Level |
We are seeking to hire multiple capable and driven entry-level Research Associates to join our tight-knit research and development team. In this position, you will be working closely with a cross-functional team of mission-driven scientists and engineers to drive the invention and development of novel diagnostic products. | 5/17/2024 |
| 2848 | AAVIS Pharmaceuticals Hoschton, GA Quality Control Chemists (Hoschton, GA) Master’s Degree in Chemistry, Analytical Chemistry, or Pharmaceutical Science. Exp: 1+ years |
Develop and optimize quality control methods for drug product and drug substances; Perform testing of raw materials, intermediates and finished product using HPLC/Empower, GC, Dissolution apparatus/Autosampler, UV/Vis, and FTIR; Perform routine testing of residual solvents for raw materials and finished products; Develop and perform method validation and method transfer for ANDA and QC methods for Assay, Dissolution, Impurities, and residual solvents per USP and ICH guidelines; Calibrate and troubleshoot HPLC system, Dissolution, PH meter and KF apparatus; Perform wet chemistry tests, including LOD, pH, titration, residue on ignition and Heavy metals in compliance with cGMP and cGLP. | 5/10/2024 |
| 2849 | Abbott Minnetonka, MN Quality Engineer I Bachelors Degree Or an equivalent combination of education and work experience. Exp: 0-2 years |
This position works out of our Minnetonka, MN location in the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. Quality Engineer I is responsible for developing and maintaining quality engineering methodologies and providing quality engineering support within new product development, manufacturing, or system/services support. | 5/10/2024 |
| 2850 | Abbott Sylmar, CA Mechanical Development Quality Engineer I Bachelors Degree Or an equivalent combination of education and work experience. Exp: 0-2 years |
This position works out of our Sylmar, CA location in the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. Mechanical Development Quality Engineer I assures new or modified products conform to quality standards and establishes compliance with the quality system. Responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success by protecting patient/user safety and meeting business needs | 5/10/2024 |
| 2851 | Abbott Sylmar, CA Development Quality Engineer I Bachelors Degree Or an equivalent combination of education and work experience. Exp: 0-2 years |
This position works out of our Sylmar, CA location in the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. Development Quality Engineer I assures products, processes, and quality records conform to quality standards and establishes compliance with the quality system. Responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success by protecting patient safety and meeting business needs. | 5/10/2024 |
| 2852 | Abbott Temecula, CA Associate Engineer - Product Performance Bachelor's degree. Exp: 0-2 years |
In this role you will identify, analyze, investigate, monitor and document patterns and trends in post marketing surveillance data as part of the CAPA system. Analyze and investigate product complaints from the field as part of post market surveillance requirements. Communicate and educate management, R&D, marketing, sales organization and other departments, as well as external customers about product performance. Ensure that information and insight gained from the investigations and corrective actions is fed back to the R&D and marketing organizations as part of the risk management and design input systems. Develop Post Market Surveillance Plans and provide engineering support for complaint investigation readiness of new products. | 5/10/2024 |
| 2853 | Abbott Sylmar, CA Risk Management Engineer I Bachelors Degree Or an equivalent combination of education and work experience. Exp: 0-2 years |
This position works out of our Sylmar, CA location in the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. Risk Management Engineer I works closely with development/manufacturing/quality engineering to establish and ensure compliance and quality for product related risk management documentation. Ensure risk management assessments and evaluations for products conform to established standards and agency regulations. | 5/10/2024 |
| 2854 | Abbott Pleasanton, CA Systems Engineer I Bachelor’s Degree in Engineering (Mechanical, Computer, Electrical, or Software), Computer Science, or related discipline. Exp: 6 months’ |
We are recruiting a Systems Engineer to join our Abbott Heart Failure team in Pleasanton, CA, where we are focused on helping people with heart failure manage their health to ultimately change and save lives. The engineer will be primarily working on the CardioMEMS HF portfolio, which remotely monitors changes in pulmonary artery (PA) pressure, which is used to prevent worsening heart failure, lower heart failure mortality rates, and improve quality of life for our heart failure patients. Systems engineering defines, designs, tests, and integrates components, disciplines, and products within the CardioMEMS HF System, including implantable sensors, external reader systems used by clinicians and patients, mobile application software, and cloud-based web applications. The System Engineer will help execute tasks during design change projects and development of next generation products, including requirements definition and management, design documentation, and system testing, verification, and validation. | 5/10/2024 |
| 2855 | Abbott Minnetonka, MN R&D Engineer I Bachelor’s degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, biological sciences, medical/clinical science or equivale Exp: 1+ years’ |
As R&D Engineer I, at our Plymouth, MN or St. Paul, MN location, you will be part of our Electrophysiology (EP) product development team focused on delivering the future in diagnostic, imaging, and ablation therapy catheters. In Abbott’s Electrophysiology (EP) division, we’re advancing the treatment of heart and vascular disease through breakthrough medical technologies, allowing people to restore their health and get on with their lives. | 5/10/2024 |
| 2856 | Abbvie North Chicago, IL Veterinary Technician AS/BS degree. CVT required. Exp: 0-4+ years |
The Veterinary Technician carries out daily activities in the vivarium and provides clinical nursing care and research support for lab animals. Works independently on weekends and holidays. Contributes to specific projects in support of Comparative Medicine initiatives. Provides exemplary animal care. Adheres to all department and AbbVie regulatory expectations, as well as USDA and FDA regulations. Provides veterinary care in support of the AbbVie drug discovery and development process. | 5/10/2024 |
| 2857 | Abbvie North Chicago, IL Associate Scientist I/II – DMPK-BA: Drug Metabolism, Pharmacokinetics, and Bioanalysis Master’s Degree or equivalent education. Exp: 0+ years |
Quantitative, Translational & ADME Sciences Department at AbbVie has an open position for an Associate Scientist II position in North Chicago, IL. The successful candidate will be responsible for non-regulated quantitative LC-MS/MS bioanalysis of small molecules from in vivo and in vitro samples, including data analysis and interpretation. | 5/10/2024 |
| 2858 | Abbvie North Chicago, IL Associate Scientist II/ Scientist I - Process Chemistry MS degree in chemistry. Exp: 0+ years |
Process Research and Development is responsible for inventing and executing the chemical processes and preparing active pharmaceutical ingredient (API) to enable clinical trials, toxicology studies and drug product development for Abbvie’s pre-clinical and clinical candidates. We create valuable intellectual property through composition of matter, chemical processes, and technology resulting in a cost-effective commercial manufacturing process. We develop the supply chain for APIs, prepare and defend CMC (Chemistry, Manufacturing and Control) regulatory content. We seek a highly motivated scientist with strong synthetic skills to work under the mentorship of a supervisor and to work in a multi-functional team environment. Opportunities may also exist to contribute to high-throughput experimentation, automation, and data science. | 5/10/2024 |
| 2859 | Abbvie South San Francisco, CA Associate Scientist II orScientist I, CMC Drug Substance Cell Line Development Group Associate Scientist II - Master’s Degree or equivalent education. Exp: 0+ years |
The Development Sciences Biologics CMC Drug Substance Cell Line Development Group in South San Francisco, CA is seeking a Scientist to join a talented and collaborative team developing CHO cell lines for GMP applications. In this laboratory position, the candidate will perform hands-on molecular characterization studies in a well-supported and dynamic environment to help advance novel therapies to human clinical studies. The work will encompass molecular, cellular, and bioprocess development studies relating to the generation and characterization of optimized CHO cell lines for production of our pipeline candidates. | 5/10/2024 |
| 2860 | Abbvie Worcester, MA Associate Scientist or Scientist I, Recombinant Production BS or MS in biology or related field. Exp: BS: 0-5+ years; MS: 0-2+ years |
Discovery Biotherapeutics at AbbVie is seeking a highly-motivated research scientist to join a dynamic team supporting biologics drug discovery. This position will impact projects through purification and characterization of biopharmaceutical products such as monoclonal antibodies in high throughput. The ideal candidate has direct experience with mammalian tissue culture, protein purification, proficiency in standard chromatography techniques, protein characterization (e.g., MS, SEC), and binding assays (e.g., ELISA and flow cytometry). The applicant should be able to analyze, document, and report data. She/he should possess excellent communication skills and be comfortable presenting in group settings. | 5/10/2024 |
| 2861 | Abeona Therapeutics Cleveland, OH Associate, Quality Control BS in biochemistry, biology, microbiology, molecular biology or other relevant discipline. Exp: 1 to 4 years |
The Quality Control Associate performs routine laboratory activities in support of GMP testing for Quality Control. Testing includes raw material, packaging components, in-process and finished product. Interacts with employees internal and external to Quality Control. | 5/10/2024 |
| 2862 | Absci Vancouver, WA Laboratory Technician Bachelor’s degree in Molecular Biology, Biochemistry, Microbiology, or a related discipline. Exp: 1+ years |
The Laboratory Technician will join the NGS Development team and support innovative research that advances Absci’s proprietary Drug Creation PlatformTM. The NGS team is integral to the success of most projects at Absci, and this role will involve delivering NGS results for library screens and strain construction. Primary responsibilities include providing core support to sequencing and analysis activities. The individual will work closely with other members of the NGS team in day-to-day sample preparation and operation and maintenance of Illumina and PacBio instruments. The individual should be able to master new laboratory skills rapidly and will take on additional technical responsibilities outside of the NGS team. This position will require the ability to work a weekend shift as needed. We seek candidates who are passionate about building a collaborative, multidisciplinary company culture and committed to making a transformative impact on our industry. To be successful in this role, the candidate should be a team player, have an innovative mindset, possess applicable technical experience, and be excited about working in a dynamic startup environment. An ideal candidate will demonstrate initiative and follow-through, a passion for scientific advancement, and a strong commitment to excellence. | 5/10/2024 |
| 2863 | Absci Vancouver, WA Research Associate II - Disease Biology Senior Research Associate: MSc in biology, cell biology, immunology or a relevant field. Exp: 1+ years |
As part of the Disease Biology Team, you will work on engineering cell lines for various programs and contribute to the development and optimization of cell-based assays, including, but not limited to, ligand-binding potency, cellular uptake, cytotoxicity, ADCC, CDC, ADCP, and proliferation assays. This role requires experience with mammalian cell culture techniques and understanding mechanism of action (MOA) assays. This position requires strategic thinking and a high level of collaboration across multidisciplinary teams within Absci. It also requires excellent communication, technical, and organizational skills and demonstrated success in delivering under tight timelines. Individuals who enjoy working with a sense of urgency and thrive in a dynamic team and high-performance culture will be successful and thrive in this role. | 5/10/2024 |
| 2864 | Accelerated Diagnostics Tucson, AZ Research Associate (Pilot Lab) BS in a scientific discipline. Exp: 1 year |
Accelerate Diagnostics is seeking a motivated Research Associate who would like to gain hands-on experience in an R&D pilot lab supporting antimicrobial susceptibility test (AST) assay development. The successful candidate will be passionate, well-organized, detail-oriented, and work independently as well as in a team environment. The candidate will spend approximately 70% of their time on basic laboratory techniques and the remaining 30% on assisting technical staff with routine lab and office work including equipment maintenance and cleaning, data entry and data management. The work schedule is Monday-Friday, 8:00 am - 5:00 pm. | 5/10/2024 |
| 2865 | Accurus Biosciences Richmond, CA Research Associate Bachelor’s or Master’s degree in Biology. Exp: 0-3 years |
The successful candidate will perform a range of duty critical to our research service business. The primary responsibility of this position is general molecular biology which includes DNA cloning, site directed gene mutagenesis, plasmid DNA preparation and DNA restriction analysis. Additional responsibilities for this position may include mammalian cell culture, protein transient production, stable cell line generation and general lab maintenance. | 5/10/2024 |
| 2866 | Astrazeneca Waltham, MA Research Associate Bioscience Immunology, Early Respiratory And Immunology BS or MS degree in biology, immunology or a relevant discipline. Exp: 1 year |
As a part of our growing Immunology Bioscience team within the Early R&I department, we are seeking a highly motivated scientist with diverse laboratory skills to join our collaborative team. This candidate would ideally have experience in immunology or related disciplines such as biology, biomedical engineering, virology, genetics or microbiology. This is a lab-based position, and the role will be based in Waltham, Massachusetts within AstraZeneca’s state-of-the-art laboratories where you will follow the science to help drive innovation and advance medicine to help improve patient lives. This position offers a unique opportunity to work in a dynamic and innovative environment developing your career at the interface of research and drug discovery. | 5/10/2024 |
| 2867 | Astrazeneca Gaithersburg, MD Associate Scientist - Viral Clearance Bachelor’s degree. Exp: 1 – 2 years |
This role will focus on viral clearance, part of the protein purification development function in the PAS department. The major responsibilities include: Design and execute studies to demonstrate virus removal or inactivation capabilities for protein purification unit operations, initially with guidance and gradually become independent. In collaboration with existing team members, plan studies, manage logistics, documentation, data verification and interpretation, report writing, and participate in regulatory submissions. Make periodic presentations in group meetings, project team meetings, and in one-on-one situations. Support purification process development, technology transfer to manufacturing sites, and production incident resolution as appropriate. Participate in new technology evaluations | 5/10/2024 |
| 2868 | Astrazeneca Lexington, MA Engineer - Downstream, Viral Vector Product Development BS or MS degree in Biological Engineering, Chemical Engineering, Biochemistry, or related discipline. Exp: 0-3 years |
The candidate contributes to the Viral Vector Product Development group through the design and execution of experiments based around downstream AAV (Adeno-Associated Virus) manufacturing processes. They will assist the purification team to generate, interpret, and present experimental data to inform and recommend process operating conditions with the goal of developing a robust and scalable manufacturing process. They will additionally draft documentation and provide expertise to assists in scale-up and tech transfer to clinical/commercial manufacturing facilities as well as submission of regulatory filings. | 5/10/2024 |
| 2869 | Astrazeneca Lexington, MA Engineer - Upstream, Viral Vector Product Development BS or MS degree in Biological Engineering, Chemical Engineering, Biochemistry, or related discipline. Exp: 0-3 years |
The candidate contributes to the Viral Vector Product Development group through the design and execution of experiments based around upstream AAV (Adeno-Associated Virus) manufacturing processes. They will assist the upstream team to generate, interpret and present experimental data to inform and recommend process operating conditions with the goal of developing a robust and scalable manufacturing process. They will additionally draft documentation and provide expertise to assist in scale-up and tech transfer to clinical/commercial manufacturing facilities as well as submission of regulatory filings. | 5/10/2024 |
| 2870 | Astrazeneca New Haven, CT Engineer II, Injectable Drug Product Development MS degree in Biochemistry, Chemistry, Chemical Engineering or related field from an accredited university. Exp: 1+ years |
The Engineer II will design and implement experiments to develop injectable drug product formulations and process characterization studies, including analyzing samples and authoring technical reports. Work on an impactful dynamic team and routinely collaborate to innovate with other members of Injectable Drug Product Development as well as other groups in Product Development and Clinical Supply! | 5/10/2024 |
| 2871 | Astrazeneca Frederick, MD Production Technician I -Day Shift BS/BA Degree in STEM field. Exp: 1+ years |
In this role, you will be responsible for the operation of processing equipment according to established SOPs, MPRs, & SPRs in accordance with cGMPs. Your duties will include solution preparation, cell culture, purification & formulation, and supporting activities. You will also train with a qualified Technician on activities related to operating process equipment with the requirement of qualification. Additionally, you will follow and execute cGMP documentation, utilize Manufacturing Execution systems (MES), contribute to problem-solving activities for non-routine activities on the production floor, and participate in continuous improvement activities for Manufacturing. Adherence to AstraZeneca values and behaviors is expected. | 5/10/2024 |
| 2872 | Astrazeneca Gaithersburg, MD Associate Specialist (Clinical Biologics) Bachelor's degree. Exp: 0+ years |
As an Associate Specialist in the Clinical production team within Biopharmaceutical Development, you’ll build broad knowledge of bioprocessing in a cGMP environment to launch your career in the biopharmaceutical industry. In this role you will take an adaptable, science driven approach to everything you do. You will become an integral part of process development, accelerating product candidates into the clinic and gaining knowledge and experience in cell culture, purification and critical support activities. Under the supervision of highly trained personnel, you will gain the process knowledge and abilities to perform large scale clinical development activities. You will join a collaborative and driven team in an extraordinary biopharmaceutical company. | 5/10/2024 |
| 2873 | Active Motif Carlsbad, CA Research Associate I-III RA I: Bachelor's degree in Biological sciences (in Molelcular Biology, Genetics, Life Sciences or related fields). Exp: 0-1 year |
Supports Epi-Services customer projects received by Operations & Services Team Performs next generation sequencing (NGS) lab bench work assigned in a time dependent, quality dependent manner Executes assigned lab bench experiments in a time dependent manner and quality dependent manner Train and follow SOP for each Assay Service Record, document and store data & results as per the SOP/receipt and logging of samples in LIMS tracker Ensure, contribute and support team goals achievements Performs regular clean-up of the lab bench space / equipment utilized Performs and follows safety requirements as outlined Keeps detailed record of lab experiments, logs of instruments utilized Sets up and follows quality control requirements Contributes and supports Group Leader with customer projects data analysis Will perform up to 4 different Assay Services with varying sample batch sizes Other duties as required and/or assigned | 5/10/2024 |
| 2874 | Adapt Immune Philadelphia, PA Manufacturing Cell Therapy Specialist Bachelor degree in a cell biology, bioengineering or medical technology related field, or equivalent experience is required. Exp: 1+ years’ |
This role will provide support for the manufacturing of gene modified autologous T-cell product at our manufacturing site in the Philadelphia Navy Yard. The Specialist will perform cell processing activities, media formulation, product sampling, and other manufacturing needs as necessary, commensurate with the level of training and experience of employee. Work is primarily in Grade B and Grade C aseptic manufacturing environment, but may also include support of process development runs in the Manufacturing Science and Technology laboratory. | 5/10/2024 |
| 2875 | Adaptive Biotech Seattle, WA Accessioning Specialist II Bachelor’s degree in Biology, Molecular Biology, Immunology or Chemistry. Exp: 1+ years |
The Biological Sample Management Accessioning Specialist II will be an entry level lab operations team member who is able to accession for the clinical or research accessioning teams or assist in sample management. This role is expected to spend approximately 90% of their time inside the lab and 10% of their time working on various tasks assigned by the department. A successful Accessioning Specialist II will complete the responsibilities described below while working to support clinical and research sample management within Molecular Laboratory Operations. Shift: Tuesday - Saturday 9:30am-6:00pm PT | 5/10/2024 |
| 2876 | Adaptive Biotech Seattle, WA Material Handler II BS/BA degree preferred. Exp: 1 year |
As a Material Handler II at Adaptive, you’ll be responsible for assisting the clinical laboratory operations and research labs maintain the right levels of inventory. We are seeking team-oriented and energetic individuals who have previous experience in highly regulated environments. Material Handlers reconcile receipts, move, store, and distribute various non-hazardous and hazardous materials, laboratory components, and business supplies. Working with closely related departments, you’ll conduct an array of activities to replenish raw materials and supplies where they are needed. | 5/10/2024 |
| 2877 | Adaptive Biotech Seattle, WA Research Associate I Bachelor’s degree in biology, molecular biology, immunology, or similar discipline. Exp: 0-3 years |
Adaptive is seeking a Research Associate I with an aptitude for learning to join our dynamic and collaborative R&D Operations team. You will join the high throughput molecular lab team to aid in the development of new and existing assays for cellular and computational biology research across Adaptive. In this job, you will master a variety of molecular biology techniques and participate in immune system profiling by next generation sequencing jointly with other researchers and computational biologists. As such, high attention to detail and willingness to learn is crucial for success in the role. | 5/10/2024 |
| 2878 | Adare Pharma Solutions Vandalia, OH 3rd Shift QC Chemist Bachelors Degree in Chemistry or related field. Exp: 1+ years |
The QC Chemist I is an essential part of the lab Quality team and will be expected to perform physical and chemical testing of intermediate and finished products according to written procedures. | 5/10/2024 |
| 2879 | Adhezion Mansfield, TX Process Engineer BS Degree in Chemical or Mechanical Engineering. Exp: 1+ years |
The Process Engineer will report to the Plant Manager. This position will lead the plants Process Improvement and EHS programs and be responsible for driving manufacturing productivity by improving process efficiencies, reducing wastes, improving quality, and increasing capacities as well as ensuring profitable growth through successful new product commercialization. Key processes in this adhesives and sealants manufacturing facility include solids conveying, mixing, compounding, chemical reactions, and packaging. Engineer will be coming in on the ground floor of a newly installed wood flooring urethane production line, with the ability to work with a diverse group of experienced operators in a positive culture environment. | 5/10/2024 |
| 2880 | Adimab Lebanon, NH Research Associate - Mammalian Cell Culture B.S. Exp: 1-3+ years |
We are seeking a Research Associate with experience in mammalian cell culture and protein expression to join our team. This role will support Adimab's novel antibody discovery, maturation, and production platform and closely interface with the Antibody Discovery, Protein Analytics, Molecular Core, and Computational Biology teams. | 5/10/2024 |
| 2881 | Adma Biologics Boca Raton, FL QA Specialist I - Product Release Bachelor's Degree required. Exp: One to two years |
The QA Specialist I - Product Release will have the primary responsibility consisting of the review of controlled documents for accuracy and completeness prior to Quality Assurance (QA) release of product. | 5/10/2024 |
| 2882 | Adma Biologics Boca Raton, FL Technician III, Manufacturing Fractionation - Night Bachelor's degree. Exp: 1+ years |
The Technician III, Manufacturing Fractionation - Night Shift position is under direct supervision of the Group Leader. This experienced position is responsible for the manufacture of plasma products through protein precipitation/separation and other tasks involving plasma receipt, plasma pooling, and protein separation. | 5/10/2024 |
| 2883 | Adma Biologics Boca Raton, FL Technician II - Manufacturing Fractionation - Night Bachelor's degree. Exp: 1+ years |
The Manufacturing Technician II, Fractionation - Night Shift position is under direct supervision of the Group Leader. This experienced position is responsible for the manufacture of plasma products through protein precipitation/separation and other tasks involving plasma receipt, plasma pooling, and protein separation. | 5/10/2024 |
| 2884 | Admera Health South Plainfield, NJ Associate Scientist I/II Bachelor’s degree in Biological Sciences or M.S. in Biological Sciences. Exp: BS: 1-3 years ; MS: 1 year |
Admera Health is looking for an Associate Scientist I/II to join our growing team! • Preparing solutions and reagents for performing assays on the bench. • Perform Next Generation Sequencing-based genomic assays on different workflows (few listed below): o RNAseq o Whole Genome Sequencing o Whole Exome Sequencing • Carry out genomic assays under Biosafety Level II Policies and in regulatory compliance. • Perform Operational Qualification and Performance Qualification on Next Generation Sequencers. • Strictly follow standard operating procedures set forth for processing biological specimens while complying with laboratory safety protocols. • Strict recordkeeping of all laboratory procedures. • Continue acquiring next generation sequencing knowledge to support molecular biology techniques. • Collaborate within the group and cross departmental to achieve goals. | 5/10/2024 |
| 2885 | ACDBio Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
This position is responsible for the developing and or formulation of standards, controls, calibrators, and intermediates in the production and development of Bio-Techne's Luminex, Q-kit, DuoSet, and Simple Plex product lines. Day to day responsibilities involve hands on work in a production laboratory running assays for ELISA and Luminex Assays. You will draft and revise standard operating procedures, manage a production schedule, and analyze assay data to further the ongoing development of new and existing products within Bio-Techne’s evolving portfolio. | 5/10/2024 |
| 2886 | ACDBio Minneapolis, MN Advanced Manufacturing Technician Bachelor degree. Exp: 1-3 year |
The responsibilities of a Manufacturing Technician are to support the laboratory staff with the process of building and manufacturing science products. This position will perform a variety of tasks within a laboratory setting that may include labeling, recording data, operating equipment, formulation and plate coating. | 5/10/2024 |
| 2887 | ACDBio Newark, CA Senior Research Associate, PAS MS in molecular biology, biochemistry, cell biology or related field. Exp: 0-2 years |
he Senior Research Associate (SRA) will serve as a key member of the ACD Professional Assay Services (PAS) department, performing RNAscope assay services for industrial, pharmaceutical, and academic sponsors to detect RNA targets of interest. An additional critical work component will be the application of immunohistochemistry (IHC) to look for specific protein targets. The position will have an opportunity to work closely with scientists and investigators from a broad customer base. It is expected that the Sr. Research Associate will independently collect and interpret data based on project expectations, which has implications for many downstream applications, such as biomarker validation and cell and gene therapy. The SRA will also be expected to independently utilize available resources for any required troubleshooting and communicate clearly with sponsors through both electronic mail and teleconference channels. The SRA must also coordinate with internal research and development (R&D) team to learn new techniques quickly and be able to adapt to shifting priorities in a fast- paced and growing start-up environment. | 5/10/2024 |
| 2888 | EyeCRO Oklahoma City, OK Research Associate I Bachelor's degree in a biology related field. Exp: 1 year |
We are looking for a Research Associate to join our team. The ideal candidate will be responsible for participating in a wide variety of animal-based activities and performing routine wet chemistry. This position plays a critical role in our mission to support groundbreaking scientific research and development. We highly value individuals who thrive in a dynamic team setting. Our team's success is built on a foundation of mutual support, shared goals, and a commitment to excellence. | 5/2/2024 |
| 2889 | Frontida BioPharm Vandalia, OH 3rd Shift QC Chemist Bachelors Degree in Chemistry or related field. Exp: 1+ years |
The QC Chemist I is an essential part of the lab Quality team and will be expected to perform physical and chemical testing of intermediate and finished products according to written procedures. | 5/2/2024 |
| 2890 | Frontida BioPharm Vandalia, OH 3rd Shift QC Chemist Bachelors Degree in Chemistry or related field. Exp: 1+ years |
The QC Chemist I is an essential part of the lab Quality team and will be expected to perform physical and chemical testing of intermediate and finished products according to written procedures. | 5/2/2024 |
| 2891 | Fujifilm Diosynth College Station, TX Manufacturing Technician II Associates degree. Exp: one (1) year |
Summary: The Manufacturing Technician III will work directly with a range of technologies. Dependent Upstream Unit: Single-Use Cell Culture Vessels/Bioreactors up to 2000L Bacterial Fermentation Culture Vessels up to 2000L Alpha Wasserman Continuous Flow Centrifuge Disposable Magnetic Mixing Bags and Totes Cell Expansion and Propagation Banking/Cryopreservation of Cell Lines and Viruses Hyperstack, Cellstack, and other Adherent Cell Technologies Plate counting, microscopic examination Monitor cultures, take samples, turn-around of bioreactor and fermenters, sterilization, and inoculation Downstream Unit: Medium to Large-scale filtration systems including Tangential Flow Filtration (TFF), Hollow Fiber Tangential Flow Filtration (HFTFF), Nanofiltration and depth filtration Medium to Large-scale Chromatographic systems (ÄKTA). Pre-Packed Columns from 1L to 100L Single use mixing systems (Pall & GE) Single Use connectivity types such as GE DAC and Colder AseptiQuik Bulk filling Aseptic process simulation and drug product filling Plate counting, microscopic examination Alpha Wasserman Continuous Flow Centrifuge | 5/2/2024 |
| 2892 | Fujifilm Diosynth College Station, TX Quality Control Visual Inspection Analyst I Bachelor of Science or Associate of Science degree preferably in Biochemistry, Chemistry, Biology or related field. Exp: 1+ year |
Summary: The Visual Inspection Analyst I will be responsible for assisting the drug product visual inspection program at FujiFilm Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory. External US Essential Functions: Perform visual inspection for Final Product Fills and Aseptic Process Simulations (APS) for AQL level inspections Participate in threshold study (POD) executions and training exercises for visual inspection Participate in particulate identifications and investigations, as required. Sub-visible particulate testing (USP <787>, <788> (Method 1 and Method 2), <789>), as appropriate Secondary functions could include: environmental monitoring (Total Air, Viable Air and Viable Surface) in a cleanroom/controlled environment, plate count enumeration and characterization, routine QC laboratory cleaning, management of inventory items for the laboratory Ensure the lab is maintained (organized, clean, & properly supplied). Perform other duties as assigned. Required Skills & Abilities: Must be able to pass a visual acuity test given upon hire, with corrective lenses if necessary. Ability to follow safety procedures outlined in the Chemical Hygiene Plan. Good attention to detail and ability to utilize problem solving/trouble shooting skills. Good computer skills. Demonstrated written and oral communication skills. Ability to multi-task and prioritize work assignments with little supervision. Strong organization and analytical skills | 5/2/2024 |
| 2893 | Fujifilm Diosynth Holly Springs, NC Manufacturing Associate 3 - Drug Product BA/BS, preferably Life Sciences or Engineering. Exp: 1+ year |
This role as Manufacturing Dssociate 3 in Drug Product, will mainly include the operation of the filling line including all the related tasks. This role will support projects, which will influence the manufacturing processes for Drug Product Manufacturing. This includes, training new colleagues, maintaining compliance of cGMP documents and assisting in the qualification of equipment as well as all other aspects of the startup of the DPFG facility. This manufacturing facility will be 24/7 operational and the role may require to be flexible with working hours and shift rotation. While in project phase, the schedule will be Monday-Friday during normal business hours. Upon transitioning to operations, this position will transition to a day or night shift that will be defined prior to the transition. During the project phase Contribute to the preparation for operational readiness related to bulk drug product manufacturing Possible assignments include, supporting projects related to procedure review and/or creation, development or transfer of manufacturing business processes and testing and commissioning support Travel up to 0-25% (international or domestic) may be required during the project phase In operations Lead, execute and document manufacturing processing steps and/or manufacturing support activities as well as process monitoring and control Perform in-process testing (pH, conductivity, visual inspection) Execute validation protocols according to cGMP Standard Operating Procedures (SOPs) Maintain training to perform all required manufacturing activities Assist and/or lead cycle counts and manage materials for the assigned manufacturing functional area Perform Operations for all aspects of filling line Assist the lead with tasks in manufacturing activities Assist with the coordination of daily shift activities This role requires shift work (weekend and potential for nights) Perform other duties as assigned | 5/2/2024 |
| 2894 | Waters Milford, MA Design Quality Engineer Minimum of a Bachelor’s degree in Engineering or Science related function. Exp: 1+ year |
This position will be responsible for concurrent quality engineering science activities associated with the consumables and lab automation product development business unit, on-market design change, risk management, quality systems and Waters requirements for columns, kits and chemistry products. Primary responsibility will be to provide chemistry/scientific and product support in the following areas: design controls, risk management, change control, post market review, quality planning, continuous improvement, establishment of appropriate requirements management and traceability. This is a Hybrid position based in Milford, MA | 5/2/2024 |
| 2895 | InBios International Seattle, WA Research Associate I A bachelor’s degree in a biologicals science. Exp: 1-2 years |
You have a biologicals, life sciences degree, academic or commercial lab experience with good simple buffer knowledge and experience and a firm scientific foundation, and you are eager to put your skills and knowledge to use in the commercial biotech assay research and development field. You also thrive in a fast-paced work environment where priorities and projects may change quickly. You are attentive and teachable and have a strong desire to learn new skills and you want hone those skills you have already begun to master under the supervision and instruction of the team’s lead scientist. You are a good teammate who is responsible and motivated and comfortable working closely in a team environment, where you openly share ideas and collaborate. You may or may not already have lateral flow immunoassay experience. (Prior experience with LFI is not required for the Research Associate I position.) | 5/2/2024 |
| 2896 | InBios International Seattle, WA Manufacturing Associate I - ELISA Bachelor’s degree with emphasis on life science OR Associate of Applied Science degree preferred but not required. Exp: 1-year |
We are searching for entry-level candidates to join our Biotech manufacturing team to support efforts in producing EUA-approved Covid-19 antigen tests and other InBios products. This position is ideal for someone who wants to start out working in a biotech laboratory/manufacturing environment, learn industry standard good manufacturing practices (GMP), is ready to learn new skills and procedures and is comfortable working with machines and with your hands. We would like to see your resume if you have general industrial or academic laboratory experience and a willingness to learn more lab skills. This position provides opportunity for working with a team and independently on a variety of tasks including preparing buffers, running semi-automated machines, and producing large-scale ELISA diagnostic test components in a BSL-2 laboratory. If you are seeking an entry-level, full-time, on-site position where you can gain experience and grow at the forefront of medical diagnostic biotechnology, this is a great opportunity for you. | 5/2/2024 |
| 2897 | InBios International Seattle, WA Manufacturing Associate I- Rapid Spray (2nd Shift 3:30PM - 12:00AM) Bachelors degree in life sciences or a similar field. Exp: 1 year |
We have an immediate opening for entry-level candidates to join our Biotech manufacturing team to support efforts in producing EUA-approved Covid-19 antigen tests and other InBios products. This position is ideal for someone who wants to start out working in a biotech laboratory/manufacturing environment, learn industry standard good manufacturing practices (GMP), is ready to learn new skills and procedures and is comfortable working with machines and with your hands. We would like to see your resume if you have general industrial or academic laboratory experience and a willingness to learn more lab skills. This position provides opportunity for working with a team and independently on a variety of tasks including preparing buffers, running semi-automated machines, and producing large-scale lateral flow diagnostic test components. If you are seeking an entry-level position with opportunities for experience and growth at the forefront of medical diagnostic biotechnology this is a great opportunity for you. This position operates on two schedules. This opportunity is for our 2nd shift, which is from 3:30 PM - 12:00 midnight Monday - Friday. | 5/2/2024 |
| 2898 | Pace Analytical Maplewood, MN Laboratory Technician Minimum requirement: Associate degree in science or equivalent laboratory experience. Exp: 1 year |
Join us as a Laboratory Technician, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. This candidate will be responsible for maintaining the lab spaces and supplies to support research and development laboratories. This includes maintaining equipment, supplies, and lab cleanliness that support the development of a variety of healthcare products. This role may include basic solution and sample preparation. | 5/2/2024 |
| 2899 | Pace Analytical Maplewood, MN R&D Lab Tech B.S. in a chemistry, biology or related area of study. Exp: 1+ years |
Join us as an R&D Lab Technician, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. A candidate for this position will have excellent lab skills across a variety of techniques to support a research lab focusing on development of medical adhesives and other devices | 5/2/2024 |
| 2900 | Pace Analytical Maplewood, MN Bioanalyst B.S. in molecular biology, biochemistry, biology, chemistry or related science. Exp: 0+ years |
Join us as a Bioanalyts, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. This candidate will be responsible for performing bioassays and application development to support biopharmaceutical filtration devices. These analyses include ELISAs, PCR, DNA and more that support cell culture production. In addition the candidate will be supporting the development of new applications of current filtration products. Join us as a Bioanalyts, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. | 5/2/2024 |
| 2901 | Pace Analytical Maplewood, MN Physical Properties Technician - Entry Level Bachelors degree in a science field. Exp: 0+ years |
Join us as a Physical Properties Technician, where you’ll put your love of science to work in the Scientific Insourcing Solutions division. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. The Scientist will prepare and test samples in the lab for adhesive products, and assist with lab maintenance | 5/2/2024 |
| 2902 | Pace Analytical Maplewood, MN Product Engineering Techician B.S. in Chemistry, Biochemistry, Materials Science or related science. Exp: 1+ years |
Join us as an Engineering Product Technician, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. This position will actively support the testing of healthcare products crucial to patient’s safety efforts within the healthcare industry. This role includes performing lab-scale polymerization reactions, coating adhesive solutions into films, and physical properties testing. Work is performed as part of a team in a fast-paced environment | 5/2/2024 |
| 2903 | Pace Analytical Maplewood, MN Laboratory Technician Minimum requirement: Associate degree in science or equivalent laboratory experience. Exp: 1 year |
Join us as a Laboratory Technician, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. This candidate will be responsible for maintaining the lab spaces and supplies to support research and development laboratories. This includes maintaining equipment, supplies, and lab cleanliness that support the development of a variety of healthcare products. This role may include basic solution and sample preparation. | 5/2/2024 |
| 2904 | Pace Analytical Brooklyn Park, MN Microbiologist Bachelor's degree in Microbiology, Biology or a related discipline required. Exp: 1 year - 4 years |
Join us as a Microbiologist, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. The main function of the QC Microbiologist is to perform supportive activities for general lab readiness, conducting critical biological tests, and following SOPs to perform methods using analytical skills and understanding of biological and chemistry techniques and principles. Note: This position is expected to last 9 months up to 1 year. Note: Training will occur for 2-3 weeks standard 8-hour days M-F. Regular schedule will be Saturday - Tuesday, 10 hour days | 5/2/2024 |
| 2905 | Vigene Biosciences Rockville, MD QC Associate I - Environmental Monitoring - 4 - 10 hour shifts, Thursday - Sunday from 8am - 6pm 1 B.S in Biology or related field. Exp: 1-2 years |
At Charles River Laboratories, we are looking for a highly motivated and energetic candidate to join our growing business in the CMO industry. The QC Associate I – Environmental Monitoring will perform microbiological testing, static and dynamic viable and non-viable monitoring of classified clean room areas to support planned or in process manufacturing processes. This position, as well as all positions in the Charles River team will require demonstration of Charles River DNA “Characteristics and Behaviors” (Care, Lead, Own and Collaborate). | 5/2/2024 |
| 2906 | Vigene Biosciences Malvern, PA Technician II Mammalian Cell Banking Bachelor's degree (B.A./B.S.) or equivalent in Biology or related discipline. Exp: 1 to 2 years |
Under direct supervision, responsible for performing basic daily laboratory and clean room tasks as they relate to the operations performed within the Manufacturing department, including mammalian cell banking and vaccine preparation activities, data analysis and writing client batch records and SOPs. | 5/2/2024 |
| 2907 | Vigene Biosciences Malvern, PA Sample Processing Materials Technician Bachelor's degree (B.A./8.S.) or equivalent in scientific discipline preferred. Exp: 1 to 3 years |
Responsible for performing a wide variety of tasks involved in sample processing and inventory management of critical components, critical laboratory supplies, specialty reagents, client-supplied raw materials, and internal and external cell banks. Performs a variety of activities related to log in, sample processing, storage, shipping of stored materials and client support | 5/2/2024 |
| 2908 | Vigene Biosciences Memphis, TN Biomanufacturing Technician I - Shift C Tuesday-Friday: 11:30am-10:00pm EG AS or BS in a scientific field strongly preferred. Exp: Zero to 1 year |
NOTE: This position is: Shift C: Tuesday thru Friday 11:30am - 10:00pm (Saturday, Sunday, Mondays off) The BioManufacturing Technician I is responsible for performing various manufacturing activities related to the start-up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to work night, weekends, and holidays. Must be able to meet physical requirements established in this job description. | 5/2/2024 |
| 2909 | Vigene Biosciences Wayne, PA Technician I Environmental Monitoring Bachelor's degree (B.S.) or equivalent in biology or related discipline. Exp: 0 to 1 year |
Responsible for performing daily laboratory tasks as they relate to the Environmental Monitoring and Contamination Control Department. | 5/2/2024 |
| 2910 | Vigene Biosciences Memphis, TN QC Specialist 1 Microbiology Bachelor's degree in biology or relevant scientific discipline preferred. Exp: 1 years |
The QC Specialist I for the QC Microbiology Department will be responsible for reviewing laboratory data, writing laboratory and environmental monitoring excursion reports, and executing simple tasks within projects/CAPAs/Change controls. The position requires the utmost attention to detail, good organizational skills, computer proficiency, and a basic understanding of microbiology and laboratory instrumentation. In addition, effective communication skills and the ability to function in a fast-paced, highly technical environment with minimal supervision are essential for success. | 5/2/2024 |
| 2911 | Pharmaceutical Calibrations and Instrumentation Indianapolis, IN Applications Engineer - FP/Sentinel - Indianapolis, IN Degree in engineering, mechanical preferred. Exp: 1+ years |
As an Applications Engineer you will assist our sales force with technical expertise for the design of fluid power systems and customer system integrations. This includes preparing hydraulic schematics, test procedures and recommend components. You will provide integral project management for these systems. | 5/2/2024 |
| 2912 | Boston Scientific Arden Hills, MN Analytical Chemist I - Extractables and Leachables Bachelor’s degree or higher in chemistry-focused field with aptitude for analytical chemistry. Exp: 1+ years |
The Analytical Chemist I will support chemical characterization (extractables & leachables) testing of medical devices. This role will involve significant hands-on laboratory work, including solution preparation and testing. The medical device products supported include products across the Boston Scientific portfolio. | 5/2/2024 |
| 2913 | Boston Scientific Arden Hills, MN R&D Technician II - 1st Shift Associates in Arts degree/diploma. Exp: 1 Year |
Executes and supports testing of implantable medical device batteries often involving specialized equipment in a laboratory environment during the design, development, and production life cycles of medical devices batteries. Your work will directly impact the quality and reliability of BSC products and improve the lives of our patients. You will be directly involved in characterizing and evaluating the performance of implantable medical device batteries. Take pride that the work you do helps save lives and improve the quality of life for millions of people around the world. | 5/2/2024 |
| 2914 | Boston Scientific Arden Hills, MN Manufacturing Tech II - 3rd Shift Associate in Arts degree/diploma. Exp: 1+ years |
Responsible for performing functions associated with all manufacturing operations, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components, subassemblies, and final assemblies. Determines and may assist in developing methods and procedures to control or modify the manufacturing process. Works with engineers in conducting experiments. | 5/2/2024 |
| 2915 | Boston Scientific Arden Hills, MN Manufacturing Tech II - 2nd Shift AA degree. Exp: 1 year |
Responsible for performing functions associated with all manufacturing operation, including manufacturing equipment support, calibration tasks, equipment optimization, OEE utilization. In battery manufacturing we have a diverse roster of equipment. You will support automation systems, electrical test equipment, laser systems, fixturing, vacuum systems, and much more. This is a great opportunity to further your technical career within a winning, people-oriented company. | 5/2/2024 |
| 2916 | Charles River Laboratories Worcester, MA Research Technician I Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months |
We have an exciting opportunity for a Research Technician I (Monday through Friday hours) at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. We have an exciting opportunity for a Research Technician I (Monday through Friday hours) at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. | 5/2/2024 |
| 2917 | Charles River Laboratories Ashland, OH Research Analyst I - Immunology Bachelor's degree (B.A. / B.S) or equivalent in laboratory science or related discipline required. Exp: Zero to two years |
We are seeking a Research Analyst 1- Immunology for our Safety Assessment site located in Ashland, OH. Essential Duties and Responsibilities: • Perform assays such as ELISA, multiplex, immunophenotyping, comet, and micronucleus. • Perform density gradient cell separations. • May act a lead/primary technician on basic studies. • Utilize micropipettes for all assays. • Perform study preparation activities including ordering supplies, preparing/verifying paperwork, and tube labeling. • Receive and log in reagents, solutions, and samples. • Prepare simple to complex lab solutions. • Assist in method development studies, method validation studies, and equipment validations as needed. • Operate, perform quality control and maintenance procedures on equipment such as microplate readers, plate washers, cell counters, multiplex instruments, flow cytometers, freezers, liquid scintillation counter, gamma counter, and eyewash stations. • Maintain clean work areas by cleaning dishes/glassware, wiping down countertops, and sweeping/mopping floor as needed. • Collect and record data in compliance with Good Laboratory Practices (GLPs), Standard Operating Procedures (SOPs), protocols, and study plans. • Input, print, and edit basic to complex data. • Prepare materials for shipment and archival. • Review documentation for quality control. • Perform all other related duties as assigned. | 5/2/2024 |
| 2918 | Leica Biosystems Vista, CA Software Engineer (Hybrid) Bachelor’s in (completed or in progress) in computer science, software engineering, or similar. Exp: 0-2+ years |
The Software Engineer for Leica Biosystems will located in Vista, CA, is hybrid, and will report to a Senior Manager, Software Development. This Software Engineer is responsible for helping perform maintenance and make modifications on existing and new software products. | 5/2/2024 |
| 2919 | Genesis Therapeutics San Diego, CA Research Associate, Biochemistry B.S./M.S. in Biochemistry, Biology, or a related field. Exp: 1 year |
Genesis Therapeutics is pioneering artificial intelligence guided rational drug design to address severe unmet medical needs for patients. Our lab in San Diego is looking for a motivated and enthusiastic candidate to support in vitro biochemical assay screening efforts. You will be producing biochemical activity & binding data using various technologies that will help drive rapid progress in our drug programs across a variety of different targets. | 5/2/2024 |
| 2920 | Genoptix Ft Myers, FL; Tampa, FL; Nashville,, FL Clinical Laboratory Technologist Bachelor’s Degree from an accredited college or university in one of the chemical, physical, or biological sciences. Exp: one year |
As a Clinical Laboratory Technologist Dry Lab you will work under general supervision and you will be responsible for accurately performing highly complex laboratory testing procedures. You will determine acceptability of specimens for testing, prepare clinical specimens and identify specimen related problems. You will also analyze specimens, review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. | 5/2/2024 |
| 2921 | Genoptix Houston, TX; Ft Myers, FL; Tampa, F, TX Clinical Laboratory Technologist II Bachelor’s Degree from an accredited college or university in one of the chemical, physical, or biological sciences. Exp: one year |
As a Clinical Laboratory Technologist I Dry Lab you will work under general supervision and you will be responsible for accurately performing highly complex laboratory testing procedures. You will determine acceptability of specimens for testing, prepare clinical specimens and identify specimen related problems. You will also analyze specimens, review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. | 5/2/2024 |
| 2922 | Genoptix Aliso Viejo, CA Clinical Laboratory Technologist- Molecular Bachelor’s Degree from an accredited college or university in one of the chemical, physical, or biological sciences. Exp: one year |
As a technologist, you will work under general supervision. You will be responsible for performing highly complex laboratory testing procedures. You will figure out acceptability of specimens for testing, prepare clinical specimens and identify specimen related problems. In this position, you will need to analyze specimens and review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. | 5/2/2024 |
| 2923 | MEDTOX Raritan, NJ Clinical Laboratory Technologist - Microbiology Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology. Exp: 1 year |
Are you an experienced Medical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". New Graduates Welcome! Pay Based on Experience -- Starting @ 28.50/hour Sign-On Bonus of $5,000 ( External Candidates Only ) The work schedule for this position will be Sunday - Thursday 10:00 pm - 6:30 am | 5/2/2024 |
| 2924 | MEDTOX Holyoke, MA Clinical Laboratory Technologist - Microbiology Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology. Exp: 1 year |
Are you an experienced Medical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Holyoke, MA. In this position, you will work in a fast-paced, customer-focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". New Graduates Welcome! The work schedule for this position will be Tuesday - Saturday 10:00 pm - 6:30 am | 5/2/2024 |
| 2925 | MEDTOX Binghamton, NY Clinical Laboratory Technician Associate degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology. Exp: 1 year |
Are you an experienced Clinical Lab Professional? Are you looking to looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team Guthrie Lourdes Hospital in Binghamton, NY. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. Pay Range: $20.40 - $40.14 + 10% shift differential on weekdays or 15% shift differential on weekends Work Schedule: 3x8 hour shifts: Weekdays, 3:00pm- 11:30pm and rotating weekends | 5/2/2024 |
| 2926 | MEDTOX Westborough, MA Clinical Laboratory Technologist - Molecular Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology. Exp: 1 year |
Pay Based on Experience -- Starting @ 26.00/hour Are you an experienced Clinical Lab Professional? Are you looking to looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, The Integrated Genetics Division of LabCorp is seeking a Molecular Technologist to join their Molecular Diagnostics team in Westborough, MA! In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. The Molecular Technologist will be responsible for performing complex molecular testing and results analysis according to established standard operating procedures. The Integrated Genetics-Westborough site processes extracted DNA from peripheral blood and prenatal samples (amniotic fluid and chorionic villi) for genetic testing. A variety of molecular genetics techniques are used to include Next Generation Sequencing, Real-time PCR, Sanger Sequencing, MLPA, Methylation PCR and Fragment Analysis to test for specific genetic diseases such as Cystic Fibrosis, Spinal Muscular Atrophy and Fragile X Syndrome to name just a few. Work Schedule: Sunday - Thursday, 7:00am - 3:30pm. | 5/2/2024 |
| 2927 | MEDTOX Lowell, MA Clinical Laboratory Technologist Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology. Exp: 1 year |
$10,000 sign on bonus (external candidates only) Are you an experienced Clinical Lab Professional? Are you looking to looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team at Lowell General Hospital Saints Campus in Lowell, MA. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. Work Schedule: Monday- Friday, 7:00am - 3:30pm & every 3rd weekend | 5/2/2024 |
| 2928 | Steris Mentor, OH Associate Scientist I Bachelor degree in Biology, Microbiology, Molecular Biology is preferred. Exp: 1-5 years |
Position Summary The Associate Scientist I will work in the Product Development team performing microbiology methodologies with several strains of BSL1 and BSL2 test organisms, including bacteria, fungi, and viruses. The position will require implementing established methodologies to evaluate the microbiocidal activity of disinfectants and sterilization processes. The position will also perform testing to develop and evaluate sterility assurance products (i.e. biological indicators). The position will require accurately maintaining, recording, and reporting test data. Additionally, applicant must possess the ability to perform and accurately document tasks according to established microbiocidal test standards, work instructions, and written protocols in a timely manner, while working both independently and within a team on multiple studies at different stages of the process. This position is located onsite in Mentor, OH. | 4/22/2024 |
| 2929 | Steris Richmond, CA Quality Engineer Bachelor Degree in Engineering or Computer Science Exp: 1+ years |
The Quality Engineer is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR, and other applicable standards. This role supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems | 4/22/2024 |
| 2930 | Steris Spartanburg, SC Quality Analyst Bachelor's Degree Exp: 1-5 years |
The Quality Analyst is responsible for assisting in administration of the quality management system at a site to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. This role leads complaint/CAPA investigations, supplier quality improvement initiatives, continuous improvement initiatives and countermeasures with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. The Analyst also supports production and quality operations by coordinating and performing problem-solving investigations, pre-reviews and final acceptance/run release of processing runs that contain non-conformances. Responsible for the activities related to quality and regulatory compliance to ensure all product processing requirements are met in accordance with Customer specifications including calibrations, dosimetry results, generation of test methods, audits, scheduling, validations, record keeping and reporting. | 4/22/2024 |
| 2931 | Stryker Portage, MI Design Engineer – Electrical, RISE B.S or M.S. in Electrical Computer Engineering, Electrical Engineering or related engineering discipline; we will only consider candidates with Decemb Exp: 0+ years |
Stryker, a global leader in medical technology takes great pride in their people, and that’s why we’re looking to expand our talent. As a result, we are looking for the best and brightest graduates to strengthen our team and drive our business going forward. The Rotational Intensive Specialized Experience (RISE) Program, which lasts 2 years and includes 4 six-month rotations, is designed specifically for highly talented engineers who are looking for exposure to and experience in different disciplines of engineering. Participants will be immersed into new product development (design engineering), quality, product testing, simulation, and so much more. Each individual’s rotations are tailored to fit their passion and skill sets along with current business needs. RISE engineers will not only gain a broad knowledge of our Research & Development functions but will also have the opportunity to attend additional leadership and personal development trainings, seminars, and product labs. The RISE Engineering program also offers exposure to senior leadership with end of rotation presentations, townhalls, and small group forums. Upon successful completion of the program, participants are eligible to apply to any open roles within Stryker. | 4/23/2024 |
| 2932 | Stryker Portage, MI Mechanical Engineer, R&D – Sustainment Bachelor’s Degree in Mechanical Engineering or related Exp: 0+ years |
Stryker is seeking to hire a Mechanical Engineer, R&D to support Medical’s Acute Care Product Engineering team. This role is onsite, in Portage, MI with the expectation to come into the office 4-5 days a week. Stryker Bed Frames Stryker Stretchers and Transport Chairs | 4/23/2024 |
| 2933 | WuXi Apptec San Diego, CA Research Associate III Master degree in Molecular and Cell Biology Exp: 0+ years |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly skilled and motivated Research Associate III to support our in vivo pharmacology team for various projects. | 4/24/2024 |
| 2934 | WuXi Apptec San Diego, CA Research Associate Must have Master’s degree in Biochemistry, Cellular and Molecular Biology, Biomedical Engineering, or Biotechnology. Exp: 1+ years |
Research Associate (San Diego, CA) – Skills and knowledge in Biological Macromolecules, Protein/ligand Binding, Cell-cell Interactions, Gene Delivery, Stem Cells Engineering, Polymer Synthesis/processing. Perform assay in cell-based format and biochemical assays using Biological Macromolecules, Protein/ligand Binding, Cell-cell Interactions, Gene Delivery, and Mammalian cell culture; Perform compound management work; Perform incucyte analysis to determine cell doubling time and seeding density for cytotoxicity study using Stem Cells Engineering, Polymer Synthesis/processing; Perform assays in cell-based format suitable for SAR screening in 96 and 386-well formats; Support cell banking and maintain cell line inventory; Execute validated assays for compound screening. | 4/24/2024 |
| 2935 | WuXi Apptec San Diego, CA Research Associate II - In Vivo Pharmacology Master degree in Molecular and Cell Biology or Bachelor degree. Exp: MS: 0 years; BS: 1 -2 year |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly skilled and motivated Research Associate II to support our in vivo pharmacology team for various projects. | 4/24/2024 |
| 2936 | WuXi Apptec San Diego, CA Research Associate II (Temp/Contingent) Master degree in Molecular and Cell Biology or Bachelor degree. Exp: MS: 0 years; BS: 1 -2 year |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly skilled and motivated Research Associate III to support our in vivo pharmacology team for various projects. | 4/24/2024 |
| 2937 | WuXi Apptec Philadelphia, PA Laboratory Technician I Associates’/Bachelor’s (science preferred) degree. Exp: 0-2 years |
The Laboratory Technician I performs cell culture and cell-biology based assays according to and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Under direct supervision, completes batch records and other required documentation and performs laboratory maintenance duties according to GLP, cGMP, CFR and/or PTC guidelines and SOPs. Performs additional Research & Development activities as required. | 4/24/2024 |
| 2938 | WuXi Apptec Cranbury, NJ Associate Scientist I (Contingent/Temp) Bachelor’s degree in animal science, biology, or a related discipline. Exp: 0-3 years |
Plans and carries out in vivo experiments and associated research assignments in rodents. Maintains the vivarium, labs, and program to AAALAC standards. Operates lab equipment including oxidizers, centrifuges, LS counters, and cage/tunnel washers. **Please note that this is a contingent/temp position and not eligible for benefits.** Schedule: Monday to Friday 6:30 AM - 3:00 PM (occasional weekend rotations | 4/24/2024 |
| 2939 | WuXi Apptec Philadelphia, PA Bioprocessing Associate I AS/BS Exp: 0+ years |
The Bioprocessing Associate I is responsible for providing support in performance of activities within production facilities to support manufacture of Master and Working Cell Banks Cell & Gene Therapy products, and final product fills according to current Good Manufacturing Practices (cGMPs). The Bioprocessing Associate I is responsible for providing support in performance of activities within production facilities to support manufacture of Master and Working Cell Banks Cell & Gene Therapy products, and final product fills according to current Good Manufacturing Practices (cGMPs). | 4/24/2024 |
| 2940 | Cel-Sci Baltimore & Elkridge, MD Validation Technician B.S. in science or engineering or a related discipline or 2-year degree. Exp: AS: 1 to 2+ years |
The Validation Technician is responsible for supporting validation activities of GMP equipment and systems. Assists in specifying and selecting equipment. Maintains all records related to qualification and validation. Prepares validation reports, suggests, and assists in determining specifications, and makes recommendations for modifications as necessary. The Validation Technician reports to the Validation Engineer. | 4/24/2024 |
| 2941 | Cel-Sci Baltimore & Elkridge, MD Validation Engineer B.S. in a related discipline. Exp: 1 to 5+ year |
The Validation Engineer is responsible for the regulation and support of equipment and systems. Assists in equipment selection, specification, and negotiating fees. Maintains all records related to qualification and validation. Works on projects where data analysis requires evaluation of defined factors to broad concepts. Utilizes independent judgment within broad parameters to determine an appropriate solution. Prepares validation reports, suggests and assists in determining specifications, and makes recommendations for modifications as necessary. The Validation Engineer reports to the Validation Supervisor. | 4/24/2024 |
| 2942 | Cogent Professionals Indianapolis, IN Pharma Lab Technician AS degree in chemistry, biology or related science and/or equivalent college coursework in the sciences. Exp: 0+ years |
We currently have a role available for a Pharmaceutical Lab Technician. Job duties include, but are not limited to, the following: General lab organization: order lab gases; put away clean glassware; refill lab solvents; maintain cleanliness and organization of labs, hallways, back-up hoods, waste disposal stations, and storage areas. Chemical preparation: Basic reagent and solvent preparation and transporting to different labs as needed. Instrument care: submit maintenance requests and coordinate with service providers; defrost lyophilizers; check balances for correct operation and appropriate cleanliness; fill liquid nitrogen for NMRs; clear NMR sample carousel; refill LC-MS solvents and QC vials; prepare LC-MS wash solvents; check LC-MS standards; routine preventative maintenance of vacuum pumps. Purification instrument duties: fill solvents and collection racks for flash systems; ensure consumables are properly stocked; dispose of waste solvents and tubes; refill wash bottles; clean and properly store reusable columns. Stockroom support: deliver chemicals from and return items to chemical inventory system; appropriately segregate chemicals; inventory reconciliation; assess safety labeling of compounds to maintain appropriate labels | 4/26/2024 |
| 2943 | Concuir Consulting Los Angeles, CA Project Engineer II/III BS Engineering degree required, Chemical, Mechanical or Biomedical preferred. Exp: 1-4+ years’ |
As a full-time employee of Concuir, Inc, you will provide consulting services to pharmaceutical, biotech and/or medical device manufacturing clients. In this role, you will quickly learn common client practices, recommend and implement improvements to reach project goals, and have the opportunity to scale-up and bring new products into manufacturing. You will be able to utilize your experience as well as benefit from Concuir’s portfolio of project management and cGxP best practices to drive your overall success. Projects range from design through qualification of production equipment, utilities modification, implementation of new facilities and process scale ups. | 4/26/2024 |
| 2944 | Cosette Pharmaceuticals Lincolnton, NC Chemist I - 1st shift and 2nd shift BS or BA in Chemistry or related science. Exp: 0+ years |
Basic Purpose: Provide technical support to plant operations Essential Functions and Responsibilities: Basic wet chemical and instrumental testing of raw materials, in-process, finished product, and stability samples Basic maintenance of instrumentation and equipment in support of laboratory testing Inventory control and maintenance of laboratory chemicals and supplies Adherence to policies of EHS Other duties as assigned by management | 4/26/2024 |
| 2945 | Cytokinetics South San Francisco, CA Research Associate I B.S. in scientific discipline. Exp: 0-2 years |
We are currently in search of a highly motivated Research Associate who possesses a strong passion for the field of Medicinal Chemistry, to become an integral part of our dynamic team. The ideal candidate will bring forth their expertise and enthusiasm to actively contribute to and enhance our ongoing efforts and initiatives in the realm of pharmaceutical research and development. | 4/26/2024 |
| 2946 | Cytokinetics South San Francisco, CA Contract - Research Associate (DMPK) Bachelor's or Master's degree in Pharmaceutical Sciences, Chemistry, Biochemistry, or a related field. Exp: 1+ years |
We are seeking a highly motivated Junior Research Associate with a focus on Drug Metabolism and Pharmacokinetics (DMPK) to join our team. The ideal candidate will contribute to our efforts in screening, plasma protein binding, and microsomal assays. This role offers an exciting opportunity to work in a collaborative and fast-paced environment, supporting the development of cutting-edge therapies for cardiovascular and skeletal muscle disorders. | 4/26/2024 |
| 2947 | Dewpoint Therapeutics Boston, MA Research Associate II - Compound Management M.Sc. or higher in Science, Chemistry, Engineering, or a related field. Exp: 1 year |
We are looking for a creative, energetic individual to join our Lead Discovery and Lead Evaluation team, working directly on compound management and lab informatics. If you’re looking to jump start your career as a Researcher while gaining experience and knowledge in a collaborative and empowering environment, this is the ideal role for you. As the ideal candidate, you will bring experience in managing inventories of both small molecules and biological materials and have a desire to build a career in an industry-leading & cutting edge HTS team. In this position you’ll be part of an energizing and supportive startup culture engaged in continuous learning, and part of an exceptional international team. This role is based at our site in Boston's Seaport district. Dewpoint offers competitive salary, great benefits, and amazing perks. | 4/26/2024 |
| 2948 | Dicerna Pharmaceuticals West Lebanon, NH Quality Control Coordinator Associate’s degree or equivalent. Exp: one (1) or more years |
This position is responsible for coordinating/supporting/assisting the Quality Control team including offsite and onsite calibrations, quality system interaction, management of sample collection and drop-off, communication of production schedule and ad-hoc testing requests, troubleshooting, performing a variety of highly diverse and complex administrative tasks and activities requiring sound planning, organization, judgement, adaptability, and accountability. This position is located in West Lebanon, New Hampshire and will require onsite work and collaboration. It is a full time (40 hour per week) position and the standard schedule is Monday-Friday (8am-5-pm). We offer a competitive salary, commensurate with experience. | 4/26/2024 |
| 2949 | Dicerna Pharmaceuticals West Lebanon, NH Manufacturing Technician Bachelors’ Degree in a science discipline. Exp: zero (0) years’ |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. | 4/26/2024 |
| 2950 | Elicio Therapeutics Boston, MA Scientist I/II, Translational Medicine MS. Exp: 0-3 years |
Reporting to the Senior Scientist I of Translational Medicine, this individual will serve as an integral team member with exposure to multiple facets of business operations. The Scientist I will be responsible for conducting immunogenicity assays that measure vaccine efficacy, such as ELISpot/Fluorospot, ICS, and other flow cytometry-based assays. As part of the organization's Translational Medicine team, this individual will interact collaboratively with the Clinical Operations and Analytical Chemistry departments to successfully progress current and future clinical programs. Additional attributes of the position include responsibility for performing in vivo mouse experiments to characterize the immune response to vaccine candidates. Elicio (ELTX) is a growing organization based out of the Seaport area of Boston, Massachusetts with additional staff functioning in a virtual-based environment from the Greater Boston area and throughout the United States. | 4/26/2024 |
| 2951 | BostonGene Waltham, MA Biospecimen Inventory Technician Minimum BS in a Biological or Life Science. Exp: one year |
The candidate will report to the Lab Manager and under their supervision support BostonGenes laboratory teams with sample management and tracking systems/protocols. The candidate will create and oversee a new sample inventory tracking system using the existing Lab Information Management System (LIMS) and Benchling software. Once created they will assist in the transition to an end-to-end barcoding-based system for sample tracking and continuously update and improve the process as new tests are added. This candidate will also be responsible for handling and processing blood specimens for specific projects. This will involve basic blood processing techniques such as blood fractionation, plasma clarification, and cell isolation for downstream biobanking. | 4/16/2024 |
| 2952 | BPS Bioscience San Diego, CA Research Associate I, Molecular & Cellular Biology Bachelor's. Exp: Entry-level |
The position requires the ability to perform and somewhat independently interpret molecular cloning and protein expression experiments. The successful candidate will be tasked with duties in molecular biology, cell culture and transfection techniques. These include standard cloning, PCR techniques, and plasmid preparation and analysis. Expression systems of focus will be mammalian cells (293). This position will include assisting other researchers with their experiments and with lab maintenance. | 4/16/2024 |
| 2953 | BroadPharm San Diego, CA QC Chemist Bachelor or MS degree in Analytical Chemistry or Organic Chemistry is required. Exp: 1-4 years |
BroadPharm is a fast-growing biotech company which specializes in providing high purity PEG products and customer services worldwide. We are seeking a highly motivated QC Chemist to join our expanding team. The ideal candidate would already have 1+ year of working experience with HPLC, MS, and NMR. The position will work closely with the production team and regulatory manager in addition to the current QC staff. | 4/16/2024 |
| 2954 | Cabaletta Bio Philadelphia, PA Research Associate/Sr. Research Associate, Molecular Biology B.S degree in Life Sciences or closely related discipline. Exp: 0-2 years |
Reporting to the Associate Scientist, Molecular Biology group, we are seeking an experienced and motivated Research Associate or Senior Research Associate. Under scientific and technical supervision, the candidate will design and execute cell-based assay advancing multiple discovery programs. The position offers growth into additional areas such as cell biology and molecular biology, immunology, and cell therapy. The position involves both technical and operational responsibilities. | 4/16/2024 |
| 2955 | Caraway Therapeutics Rahway, NJ Specialist, Process Engineering Bachelor’s degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field. Master’s degree in Chemical Engineering, Ch Exp: BS: 1 year |
The Process Engineer role at the Specialist level will serve as a leader in the FLEx Sterile GMP Clinical Manufacturing facility. As the facility is nearing the completion of its construction, the selected candidate will contribute to equipment and facility commissioning/qualification, regulatory certification, as well as other workstreams’ critical activities to enable facility startup and operational readiness. To support these business-critical activities, night and weekend work may be required. Once the facility is operational, this role will support formulation and process development, scale-up activities, quality investigations, change management and authoring GMP standard operating procedures and protocols in support of sterile clinical drug product operations. This individual will collaborate closely with the formulation scientists, engineers, quality representatives, and other team members to ensure the quality of the clinical supplies, the scientific rigor of the processes, and ultimately to enable the flexibility and speed of our Company's pipeline. The role is based in New Jersey and reports to the Sterile Process Engineering Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply. | 4/16/2024 |
| 2956 | Caraway Therapeutics Rahway, NJ Specialist, Process Engineer - Oral Solid Dosage, Clinical Manufacturing Bachelor’s degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences or related field. Master’s degree in Chemical Engineering, Chemistry, Ph Exp: BS: 1 year |
The Process Engineer role at the Specialist level will serve as a leader in the FLEx Oral Solid Dosage GMP Clinical Manufacturing facility. This role will support formulation and process development, scale-up activities, quality investigations, change management and authoring GMP standard operating procedures and protocols in support of oral solid dosage clinical drug product operations. This individual will collaborate closely with the formulation scientists, engineers, quality representatives, and other team members to ensure the quality of the clinical supplies, the scientific rigor of the processes, and ultimately to enable the flexibility and speed of our Company's pipeline. The role is based in New Jersey and reports to the Oral Solid Dosage Process Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply. | 4/16/2024 |
| 2957 | Bayer Luling , LA Chem Production Engineer Bachelor’s of Science degree in Chemical Engineering, including May 2024 B.S. Chemical Engineering graduates. Exp: 0-3 years |
The Chemical Production Engineer provides support to plan, coordinate, and execute technical activities needed to support manufacturing operations. Also, ensures the safe, efficient, productive, and environmentally sound manufacture of active ingredients or intermediates. | 4/17/2024 |
| 2958 | Bayer Berkeley, CA Associate Electrical Engineer M.S. Degree in Electrical Engineering or related discipline. Exp: 0-1 years |
Exciting and challenging electrical engineering opportunity where each day is different. Tasks would include evaluating electrical capacity, emergency power readiness, equipment maintenance, alternative sustainable energy solutions, and component electrical ratings analysis. Interact with cross-functions including Quality, Production, Procurement, Investment Management, Research and Development at the at the local, regional, and global levels as well as external vendors, and CA state supplier. | 4/17/2024 |
| 2959 | Bayer Huxley, IA Agronomic Research Specialist II (Field) - Huxley, IA Bachelor’s degree completed by start date. Bachelor’s or Master’s degree in agronomy, life sciences, engineering. Exp: 1+ years |
As a field-facing Agronomic Research Specialist II, you will be responsible for contributing to an R&D Field Trial program for corn and soybeans. Your primary responsibilities will be to coordinate with growers on leased land space and assist with acquiring and supervising local staffing during in-season activities. You will conduct in-season research activities such as phenotyping, study management, and data analytics review as part of overseeing and executing research trials that feeds the R&D pipeline. Additionally, you will have the opportunity to partner with other Agronomic Research Specialists on site, as well as other cross-site functions on initiatives to improve data quality, standard operating procedures, or quality/compliance actions. This is an onsite role (site and surrounding production fields), primarily day shift (with extended hours during peak season) at our Huxley, IA research facility.As a field-facing Agronomic Research Specialist II, you will be responsible for contributing to an R&D Field Trial program for corn and soybeans. Your primary responsibilities will be to coordinate with growers on leased land space and assist with acquiring and supervising local staffing during in-season activities. You will conduct in-season research activities such as phenotyping, study management, and data analytics review as part of overseeing and executing research trials that feeds the R&D pipeline. Additionally, you will have the opportunity to partner with other Agronomic Research Specialists on site, as well as other cross-site functions on initiatives to improve data quality, standard operating procedures, or quality/compliance actions. This is an onsite role (site and surrounding production fields), primarily day shift (with extended hours during peak season) at our Huxley, IA research facility. | 4/17/2024 |
| 2960 | AstraZeneca Frederick, MD Production Technician I - Night Shift BS/BA degree preferred. Degree in STEM field. Exp: 1+ years |
In this role, you will be responsible for the operation of processing equipment according to established SOPs, MPRs, & SPRs in accordance with cGMPs. Your duties will include solution preparation, cell culture, purification & formulation, and supporting activities. You will also train with a qualified Technician on activities related to operating process equipment with the requirement of qualification. Additionally, you will follow and execute cGMP documentation, utilize Manufacturing Execution systems (MES), contribute to problem-solving activities for non-routine activities on the production floor, and participate in continuous improvement activities for Manufacturing. Adherence to AstraZeneca values and behaviors is expected. | 4/17/2024 |
| 2961 | AstraZeneca Frederick, MD Production Technician I/II - Nights BS/BA degree preferred. Degree in STEM field. Exp: 0-1 years |
Your responsibilities will include operation of processing equipment according to established SOPs, MPRs, & SPRs in accordance with cGMPs. You will be expected to demonstrate advanced equipment/process knowledge to diagnose issues and participate in first-line troubleshooting and root cause analysis. You will also be responsible for maintaining qualifications in Production Technician duties, executing work orders within the system, and leading continuous improvement initiatives. | 4/17/2024 |
| 2962 | AstraZeneca Frederick, MD Production Technician II-Night Shift BS/BA degree preferred. Degree in STEM field. Exp: 0-1 years |
As a Production Technician, you will be responsible for the operation of processing equipment according to established SOPs, MPRs, & SPRs in accordance with cGMPs. Your duties will include solution preparation, cell culture, purification & formulation, and supporting activities. You will also be a qualified trainer on-the-floor, follow and execute cGMP documentation, maintain qualifications in Production Technician duties, and utilize Manufacturing Execution Systems (MES). Furthermore, you will contribute to problem-solving activities and troubleshooting for non-routine activities on the production floor. You will lead indirect processing activities in support of MFG operations and continuous improvement initiatives. Adherence to AstraZeneca values and behaviors is a must. | 4/17/2024 |
| 2963 | Bachem Vista, CA Process Engineer Bachelor’s degree in mechanical, electrical, chemical, manufacturing engineering or science related field. Exp: 1-3 years |
The process engineer is responsible for supporting and maintaining critical and supporting equipment and instruments to ensure the manufacturing process is continuously in operation with minimal downtime. Concurrently, through process mapping, the process engineer is responsible to develop process improvement projects to create efficiency in the process. The process engineer will also be responsible for identifying and researching background for equipment purchases and making recommendation to management. | 4/18/2024 |
| 2964 | Covance Burlington, NC Molecular Diagnostic Specialist for DNA Identification Bachelor's Degree in Biology, Chemistry or Life Science. Exp: 1 year |
The DNA Identification Building in Burlington, NC is seeking a Molecular Diagnostic Specialist. The Molecular Diagnostic Specialist helps to support the operations team, the quality team and the laboratory in various ways while also maintaining the laboratory equipment and their records. As a Molecular Diagnostic Specialist, this role will help support the development and optimization of new and existing molecular diagnostic tests. Conducts routine to complex experimental procedures within overall scope of a research project and/or diagnostic test development project. Maintains all appropriate records regarding data collection and interpretation of results. Daily activities include scripting for automation, validation of equipment and consumables, general instrument repairs, and monitoring PMs. The MDS team is vital in constant lab streamlining and preventing down time in lab processing. LabCorp's Consumer Genetics operation is one of the world's largest genotyping facilities, having genotyped millions of samples for SNP (Single Nucleotide Polymorphism) analysis since 2013. SNPs are single base changes in DNA that give rise to genetic variation. These variations can be used for ancestry typing, health and disease risk factors, carrier conditions, and curiosity testing! The working schedule for this position will be: Monday - Friday 2 pm - 10:30 pm, 10% shift differential offered for 2nd shift. | 4/18/2024 |
| 2965 | Covance Burlington, NC Technologist for Moleclar Micro Bachelor's degree in Biology, Chemistry, Medical Technology or a related science. Exp: 1 year |
Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our lab team as a Technologist in Burlington, NC. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives." This position is also responsible for supporting the COV2 team to include duties such as assay building and releasing results. The schedule for this position will be: 2nd shift, Tuesday-Sat, 2:00pm-10:30pm. Eligible for 10% shift differential due to 2nd shift hours. | 4/18/2024 |
| 2966 | Covance Raritan, NJ Clinical Laboratory Technologist - Molecular Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) require Exp: 1 year |
Are you an experienced clinical laboratory professional looking for leadership opportunity? Are you detail oriented, process focused, and enjoy leading others? Are you looking for an industry leading company that offers growth and stability? LabCorp is seeking a Clinical Laboratory Technologist to join our Core Laboratory team in Raritan, NJ. In this position, you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". Work Schedule: Tuesday - Saturday: 3:00 pm - 11:30 pm | 4/18/2024 |
| 2967 | Covance Raritan, NJ Clinical Laboratory Technologist - Chemistry Bachelor’s degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) require Exp: 0+ years |
Are you an experienced Clinical Lab Professional? Are you looking to looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team in Raritan NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. Work Schedule: Work Schedule: Tuesday - Saturday (12:00am - 8:30am) and alternating Saturdays (11:30pm- 8:00am) New Grads Welcome – Full Training Provided | 4/18/2024 |
| 2968 | Covance Raritan, NJ Clinical Laboratory Technologist - Microbiology Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) require Exp: 1 year |
Are you an experienced Medical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". New Graduates Welcome! Pay Based on Experience -- Starting @ 28.50/hour Sign-On Bonus of $5,000 ( External Candidates Only ) The work schedule for this position will be Sunday - Thursday 10:00 pm - 6:30 amAre you an experienced Medical Lab Professional? | 4/18/2024 |
| 2969 | Covance Raritan, NJ Clinical Laboratory Technologist - Forensics Toxicology Bachelor’s degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet localregulatory (CLIA & State) requirem Exp: 0+ years |
Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. New Grads Welcome - Full Training Required Work Schedule: Tuesday – Saturday - 7:00 am - 3:30 pm | 4/18/2024 |
| 2970 | Covance Holyoke, MA Clinical Laboratory Technologist - Microbiology Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) require Exp: 1 year |
Are you an experienced Medical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Holyoke, MA. In this position, you will work in a fast-paced, customer-focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". New Graduates Welcome! The work schedule for this position will be Tuesday - Saturday 10:00 pm - 6:30 am | 4/18/2024 |
| 2971 | Dexcom San Diego, CA Mechanical Engineer II Master’s degree in a technical discipline. Exp: 0-2 years’ |
The R&D Mechanical Engineering Characterization Team is responsible for the feasibility and development of next-generation products at Dexcom. We’re seeking a cross-functionally disciplined engineer with subject matter expertise across mechanics, materials, and human tissue/device interaction to support characterization and test of novel patch materials and designs. Positioned within the Mechanical Engineering team, this is a high visibility, high impact role in achieving Dexcom’s product performance and reliability goals through delivering functional excellence in the research, development, and characterization of technologies/designs & their integration to a product ecosystem. | 4/18/2024 |
| 2972 | Emergent BioSolutions Baltimore, MD Analyst II, Quality Assurance - 3rd-Shift BS or BA degree in Science or Engineering. Exp: 0-2 years |
The Analyst II on the Floor is responsible for assuring the quality of products manufactured at the Emergent BioSolutions Baltimore Facility. The Analyst II will perform Quality on the Floor functions. Our QA Department provides expertise in problem-solving and process improvements. The QA Specialist will interact with manufacturing personnel and Quality Engineers to provide guidance necessary to maintain and improve CGMP compliance at the company. | 4/18/2024 |
| 2973 | Emergent BioSolutions Baltimore, MD Analyst II, QA on the Floor BS or BA degree in Science or Engineering. Exp: 0-2 years |
This role is responsible for monitoring Warehouse areas, Printed Material inventory management,Packaging Operations support, and Warehouse Quality on the Floor continuous improvement. | 4/18/2024 |
| 2974 | Emergent BioSolutions Baltimore, MD Analyst II, QC Microbiology, 3rd Shift (Wed-Sat) MS in Microbiology/Biology or related field. Exp: 0-2 years |
The Analyst II, QC Microbiology position supports the Quality Control group at Emergent BioSolutions Camden Campus to maintain process optimization and manufacturing activities. The Microbiologist is responsible for performing activities in support of the Microbiology, Environmental Monitoring, and Utility testing programs, which includes microbiological product testing, monitoring of the manufacturing production space, and supporting quality initiatives. The individual routinely conducts monitoring, testing, and SOP generation and revision. This is a 3rd-shift/4 day work week position -working hours 10pm-8:30am-Wednesday through Saturday. Hours may vary to meet business and training needs. | 4/18/2024 |
| 2975 | Emergent BioSolutions Winnepeg, MB, CA Analyst I, QC Laboratory Services - Limited Term University degree or technical diploma in microbiology, biology or related field of study. Exp: 0-2 years |
The Analyst I, QC Laboratory Services performs GMP compliant microbiological testing as required to support Raw Material testing, In-process, Finished Product release & Stability or nonclinical/ clinical studies. The Analyst I may also perform testing required to support assay and process validations. He/She will perform testing to support release of lab specific material (media, standards). | 4/18/2024 |
| 2976 | Emergent BioSolutions Rockville, MD Sr Bioprocess Associate BS/BA in Biology, Chemistry, or related discipline. Exp: 1-3 years’ |
The primary role of this position is to provide technical support for all fill finish operations with strict adherence to cGMP compliance. The candidate will also provide guidance for all on-floor activities including aseptic fill operations, visual inspection, labeling, and packaging of bulk product with minimal supervision. This position requires proficiency in aseptic technique, and deliberate movements inside various isolators. The candidate for this position will be working in close association with Technical Operations, Quality Assurance, Quality Control, and Material Management to overcome challenges in meeting the production schedule. | 4/18/2024 |
| 2977 | Leidos Biomedical Research San Antonio, TX Research Associate Master’s degree or equivalent. Degree should be in a related field. Knowledge of animal anatomy and physiology. Exp: 1+ years |
Are you ready for an opportunity to make a difference in the lives of those who serve our country? Leidos Health Solutions is currently looking for a Research Associate with molecular biology experience to support the Directed Energy (DE) department at the Naval Medical Research Unit, San Antonio (NAMRU-SA) in San Antonio, TX. NAMRU-SA conducts gap driven combat casualty care, craniofacial, and directed energy research to improve survival, operational readiness, and safety of Department of Defense personnel engaged in routine and expeditionary operation. | 4/19/2024 |
| 2978 | Leidos Biomedical Research Dayton , OH Electrical Engineer Bachelor’s degree in an engineering discipline (electrical, computer, or similar). Master’s degree or higher in electrical or computer engineering. Exp: BS: 0-3 years |
Leidos is searching for an Electrical Engineer to support AFRL’s Dynamic Infrared Missile Evaluation (DIME) Laboratory located on Wright Patterson Air Force Base, OH. The successful candidate will utilize a strong engineering background designing, testing, modeling, simulating, and analyzing the next generation of infrared countermeasure techniques. This position will support multiple simultaneous research efforts within the laboratory requiring skills including hands-on experimentation, digital modeling using graphical programming, modeling and simulation of aircraft/missile engagements, and computer application development involving interfacing with hardware systems and real-time processing. Addressing our customers’ challenging mission requirements necessitates research and development of new capabilities as well as making improvements to existing systems. The successful candidate will be required to quickly develop an understanding of legacy efforts and engineer improvements to meet new requirements. Additionally, the engineer will be called upon to develop new and innovative solutions to challenging problems, helping our customers provide solutions for the warfighter. The successful candidate will work as part of an integrated team but should also be proficient at conducting independent research. | 4/19/2024 |
| 2979 | Leidos Biomedical Research Huntsville, AL Entry-Level Firmware Engineer Bachelor of Science in Electrical Engineering or equivalent degree from an ABET-accredited institution with a 3.0 or higher GPA. Exp: 1+ years |
Primary Responsibilities In this role, project assignments could be focused in one or multiple of the following areas: Design, simulation, and testing of firmware using hardware description languages (HDL) to drive custom hardware. Testing and integration of RF electronics such as high speed DACs used for waveform generation and ADCs used for signal processing. Utilizing cutting edge AMD/Xilinx FPGA and SoC families and design tools such as the RFSoC. Testing and debugging hardware using lab equipment such as spectrum analyzers and oscilloscopes. Working on multidisciplinary teams to debug problems when integrating firmware and PCB designs with Radar and Seeker hardware. | 4/19/2024 |
| 2980 | Leidos Biomedical Research Huntsville, AL Penetration Tester- Entry Level Master’s degree in Cyber Security, Computer Science, Computer Engineering, Electrical Engineering. Exp: 1+ years |
Leidos Defense Systems is seeking a full-time, talented, and motivated Penetration Tester to perform penetration tests on customer systems in the defense, space, cyber, and commercial fields. The ideal candidate will possess technical skills in networking, operating systems, and programming, as well as the ability to think creatively about potential threats. They will also possess the ability to analyze both open and closed-source intelligence to determine potential cyber threat Tactics, Techniques, and Procedures (TTPS), attack vectors, and risks to systems of various size and complexity. | 4/19/2024 |
| 2981 | Leidos Biomedical Research Patuxent River, MD Junior Network and Computer Systems Administrator (ROD) Bachelor’s Degree in Computer Science, Mathematics, or Engineering from an accredited college or university. Exp: 1+ years |
The Leidos Defense Group is seeking an entry level Network and Computer Systems Administrator to provide networking support as part of the Range Operations Division (ROD) Range Support Branch of the Atlantic Test Range (ATR) in Patuxent River, Maryland. Members of this dynamic team design and develop complex hardware and software network architectures to support real-time Research, Development, Test, & Engineering (RDT&E) test and fleet training events conducted by ATR in support of customers’ requirements. | 4/19/2024 |
| 2982 | Eli Lilly Indianapolis, IN Biologist - In Vivo Neuroscience BS/MS in Biology, Animal Sciences, Pharmacology, or a related field. Exp: 1+ years |
Lilly Neuroscience is seeking an experienced scientist (Bachelors or Masters) to join the Neurodegeneration team to facilitate its mission of discovering novel medicines for the treatment of Alzheimer’s disease, Parkinson’s disease, ALS, and other related neurodegenerative conditions. The individual will join a laboratory focused on in vivo research to support our expanding neurodegeneration portfolio, and they will leverage their technical expertise to lead high quality studies and sample collection to support identification/development of novel targets for Neurodegenerative conditions. A key focus of the scientist will be the utilization of multiple in vivo techniques including complex surgical models to support therapeutic investigations in pre-clinical animal models. Importantly, the individual will collaborate with colleagues across the Neurodegeneration group to facilitate both exploratory and portfolio workstreams. The scientist must possess a strong work ethic and an ability to quickly master numerous new techniques. Lilly has a proud record of drug development for neurodegenerative diseases that has been driven by a highly collaborative and diverse team of accomplished scientists. | 4/19/2024 |
| 2983 | Eli Lilly Indianapolis, IN Associate Biologist BS or MS in biology/animal science/veterinary technology or a closely related field. Exp: 1 year |
The Lilly Diabetes, Obesity and Complications Therapeutic Area (DOCTA) is focused on discovery and development of new therapeutics for the treatment of medical complications arising from type 2 diabetes and obesity. The cardiorenal team is looking for a biologist to conduct experiments using animal models of renal and metabolic diseases. The ideal candidate should be goal-oriented and dedicated, capable of conducting thorough research studies with minimal oversight. This biologist will design and perform experiments independently and within team-based environments, as well as interact with internal and external collaborators. Are you ready to actively engage in cardiorenal drug hunting teams and serve as a scientific and technical advisor to project teams? Apply now to join the Lilly Team! | 4/19/2024 |
| 2984 | Eli Lilly Boston, MA Associate Scientist, Early Preclinical Development - Inner Ear Biology Bachelor's Degree. Exp: 0+ years |
The Early Preclinical Development (EPD) Team is seeking an Associate Scientist with experience in inner ear histology to support discovery and IND-enabling animal studies. The ideal candidate will have experience in histologic techniques specific to the inner ear, such as microdissection of the mouse and non-human primate (NHP) inner ear tissues into discrete anatomical regions, and further processing of these tissues using various histologic techniques, in addition to imaging, analysis, and preparation of data for presentation. Cross-functional work may be required to advance Company goals. The successful candidate will be self-motivated and creative, with a desire to succeed at the highest level in a highly collaborative and fast-paced environment. | 4/19/2024 |
| 2985 | Eli Lilly Cambridge, MA Scientist - In Vivo Surgical Associate Bachelors or Masters degree in neuroscience or related fields preferred. Exp: 1+ years |
The Next Generation Therapeutics group is a newly formed team with a focus on using novel therapeutic modalities to deliver medicines for chronic pain and neurodegenerative disorders. The group, based at our Cambridge Innovation Center in Kendall square, will work with internal and external partners to identify, and deliver new novel therapies into patients at speed. The team is seeking experienced and inspiring scientists to join our fast-paced, interdisciplinary team as we leverage innovative RNA/oligonucleotide/gene and genomic based therapeutics to enhance our portfolio. | 4/19/2024 |
| 2986 | Eli Lilly Lebanon, IN Manufacturing Scientist - Lebanon API Manufacturing Master's Degree in STEM Discipline (Chemistry preferred). Exp: 1 year |
The Manufacturing Scientist is part of the TSMS (Technical Services/Manufacturing Science) team that provides the technical support required to achieve reliable and compliant manufacturing of API molecules. This role will be part of the Manufacturing Process Team for its respective area, providing daily oversight to ensure safe and reliable supply of medicines. The Manufacturing Scientist executes technical projects (experimental, modeling and/or production data analysis) to improve and optimize process control, yield, purity, and/or productivity. In addition, the manufacturing scientist should be capable and of setting up and executing a variety of experiments at laboratory scale and conducting research on manufactured product for process improvements and troubleshooting in the technical services and manufacturing sciences laboratory. | 4/19/2024 |
| 2987 | Eli Lilly Lebanon, IN Associate- Laboratory Support - Quality Control - Advanced Therapies Bachelors (4-year) degree in a science field related to chemistry, microbiology, biology, or other science discipline. Exp: 1+ years |
The Laboratory Support Associate is a support role in the Quality Control Laboratory helping to ensure proper and efficient functioning of laboratory operations. The Laboratory Support Associate is responsible for operational excellence and continuous improvement in the laboratory. They will manage laboratory samples, materials, reagents, equipment usage, ordering, organization, and may include management of laboratory system access. | 4/19/2024 |
| 2988 | Eli Lilly Lebanon, IN Process Engineer - API Manufacturing Bachelor's Degree in Chemical, Biochemical, Bioprocess, Process, or Mechanical Engineering. Exp: 1+ years |
We are seeking Process Engineers to support the API Manufacturing Business in Lebanon. Process Engineering is core to delivering our product pipeline across batch and continuous API production and development. | 4/19/2024 |
| 2989 | Meridian Medical Technologies Cambridge, MA Associate Scientist, Protein Production & Engineering, BioMedicine Design Bachelor’s degree is required with a Life Science major. Exp: 0 to 3 years |
Pfizer’s BioMedicine Design (BMD) is seeking a highly motivated Cell and Molecular Biologist to join Biotherapeutics Expression and Purification group (BEP) located in Pfizer Worldwide Biotherapeutics Research campus of Cambridge MA. Qualified candidate will play an essential role in support of large-scale non-GMP transient protein lead production across Pfizer’s diverse biotherapeutics discovery portfolio to enable Pfizer’s research units and their pre-clinical therapeutics in-vitro and in-vivo needs. This individual will work in the area of therapeutic protein production and engineering in mammalian cells. The individual will perform mammalian cell culture, molecular biology, large-scale mammalian cell expression, and protein production analysis for supporting protein therapeutics discovery efforts. The individual will perform this function with supervision, toward considerable independence, and will display initiative in learning new techniques. The candidate will contribute to the group wide deliverables and be required to work on several projects simultaneously presenting results and updates at group meetings. | 4/19/2024 |
| 2990 | Meridian Medical Technologies Andover, MA Associate Scientist, Cell Line Development B.S in cellular/molecular biology or related life science field. Exp: 0-3 years |
A technical, lab-based position is available within Pfizer’s Molecular and Cellular Technologies organization. The position will be primarily involved in mammalian cell line development (CLD) portfolio advancement, novel technology development and process optimization. Working with a group of scientists, the successful candidate will be responsible to perform platform cell line development activities to fulfill the need of moving Pfizer’s biotherapeutics pipeline projects towards either clinical or commercial developmental phase. This role will involve all aspects of cell line development from vector design/construction, cell culture maintenance, clone screening, and cell line characterization. The successful candidate will possess excellent aseptic technique and have experience with mammalian cell culture and recombinant protein expression. | 4/19/2024 |
| 2991 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
This position is responsible for the developing and or formulation of standards, controls, calibrators, and intermediates in the production and development of Bio-Techne's Luminex, Q-kit, DuoSet, and Simple Plex product lines. Day to day responsibilities involve hands on work in a production laboratory running assays for ELISA and Luminex Assays. You will draft and revise standard operating procedures, manage a production schedule, and analyze assay data to further the ongoing development of new and existing products within Bio-Techne’s evolving portfolio. | 3/27/2024 |
| 2992 | Advanced Cell Diagnostics Minneapolis, MN Advanced Quality Technician An associate degree. Exp: 0+ years |
The responsibilities of an Advanced Quality Technician are to perform tasks in the process of inspecting and testing science products. Duties may require interpreting results, inventory, and participation in complaint investigations. This position will participate in the continuous improvement of our products and customer-centered culture. | 3/27/2024 |
| 2993 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate MS degree in the biological sciences. Exp: 0-2 years |
As an Advanced Research Associate you will work in the Immunocytochemistry Department on the validation of antibodies for immunocytochemistry applications. You will be knowledgeable of animal anatomy and histology and familiar with histological examination of tissues, frozen and paraffin-embedded tissue sections, immunohistochemistry protocols, microscopy systems; collect digital images, digital image post-processing and enter data into a database. | 3/27/2024 |
| 2994 | Advanced Cell Diagnostics Minneapolis, MN Advanced Manufacturing Technician Bachelor degree. Exp: 1-3 year |
The responsibilities of a Manufacturing Technician are to support the laboratory staff with the process of building and manufacturing science products. This position will perform a variety of tasks within a laboratory setting that may include labeling, recording data, operating equipment, formulation and plate coating. | 3/27/2024 |
| 2995 | Advanced Cell Diagnostics Newark, CA Senior Research Associate, PAS MS in molecular biology, biochemistry, cell biology or related field. Exp: 0-2 years |
The Senior Research Associate (SRA) will serve as a key member of the ACD Professional Assay Services (PAS) department, performing RNAscope assay services for industrial, pharmaceutical, and academic sponsors to detect RNA targets of interest. An additional critical work component will be the application of immunohistochemistry (IHC) to look for specific protein targets. The position will have an opportunity to work closely with scientists and investigators from a broad customer base. It is expected that the Sr. Research Associate will independently collect and interpret data based on project expectations, which has implications for many downstream applications, such as biomarker validation and cell and gene therapy. The SRA will also be expected to independently utilize available resources for any required troubleshooting and communicate clearly with sponsors through both electronic mail and teleconference channels. The SRA must also coordinate with internal research and development (R&D) team to learn new techniques quickly and be able to adapt to shifting priorities in a fast- paced and growing start-up environment. | 3/27/2024 |
| 2996 | Advanced Cell Diagnostics Minneapolis, MN Research Associate Bachelor’s degree in the biological sciences or equivalent. Exp: 0 to 2 years |
The responsibilities of this position are production, bottling, and packaging of methylcellulose, methylcellulose-containing media, and stem cell and gene therapy (SCGT) media. Perform QC testing and analysis of some methylcellulose-containing media. Perform cell culture of multiple cell lines. Production of components for additional stem cell, and non-stem cell kits. Perform additional duties as assigned. Skills used include cell culture, high attention to detail, strong communication and organizational skills. | 3/27/2024 |
| 2997 | Advanced Cell Diagnostics Minneapolis, MN Research Associate Bachelor’s degree in a related field. Exp: up to 3 years |
Are you passionate about science, an adaptable self-starter with an insatiable curiosity and have a drive to innovate and further develop your skills with a multitude of analytical tools to study and characterize biomolecules? As a Research Associate in the Analytical Services team, you will be responsible for performing routine Quality Control (QC) testing, and participating in troubleshooting efforts for released products and new products that are still in development through the application of biophysical analysis of proteins and antibodies focusing on our capillary electrophoresis systems, but may also include chromatography, immunoassays, light scattering and other analytical tools, with the aid of fully defined SOPs. You will also actively take part in group projects, participate in process improvement efforts to improve lab protocols with the goal of facilitating innovation, efficiency and productivity, and perform additional duties as assigned. | 3/27/2024 |
| 2998 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Manufacturing Associate I - Mid-Shift Bachelors in a science or engineering discipline preferred. Exp: zero to two (2) years |
We are currently seeking a Drug Product Manufacturing Associate I who is responsible for executing GMP production of injectable pharmaceuticals by following all applicable SOP's. Manufacturing associates are responsible for preparing equipment and materials for GMP aseptic production and operating equipment such from glasswashers, autoclaves, depyrogenation ovens and automated filling machines. | 3/27/2024 |
| 2999 | Akcea Therapeutics Carlsbad, CA Research Associate II/ Senior Research Associate, Core Antisense Research Master’s degree preferred in biochemistry, molecular biology or cell biology, or a B.S. Exp: MS: 0+ years; BS: >1-2 years |
We are seeking a highly qualified and motivated individual to perform basic research to increase our understand on how ASOs target RNA to modulate the expression of genes. The position offers the opportunity to do groundbreaking science and make discoveries that will create the next generation of ASO medicines. The selected candidate will become an integral part of an interdisciplinary and energetic team of scientists in the Ionis Core Research group. | 3/27/2024 |
| 3000 | Akouos Indianapolis, IN Analytical Chemist - Bioproduct Research & Development MS in Analytical Chemistry, Biochemistry, Chemistry, or a related field. Exp: 0+ years |
The Bioproduct Research and Development (BR&D) organization delivers new medicines to patients through the development and commercialization of insulins, peptides, oligonucleotides, monoclonal antibodies, novel therapeutic proteins, and gene therapy systems. BR&D is a multidisciplinary group with deep technical expertise that works collaboratively with our discovery and manufacturing colleagues. Located in Indianapolis, IN, scientists have full access to Lilly’s deep pharmaceutical development expertise and engineering capabilities. In this role, you will be part of a diverse team of analytical chemists, pharmaceutical scientists, and engineers delivering product and process understanding across a broad range of platforms. Ideal candidates will possess experience across multiple analytical techniques, demonstrate an aptitude in technical problem solving, and be motivated to work both independently and collaboratively in a dynamic environment. | 3/27/2024 |
| 3001 | Akouos San Francisco, CA Research Associate - DMPK BS or MS in chemistry. Exp: 0-6 years |
We seek an exceptional full-time lab-based Research Associate to join our Drug Metabolism and Pharmacokinetics (DMPK) team. This individual will be a key contributor to performing standard ADME/DMPK assays, such as microsomal stability, plasma protein binding, and metabolite identification. The individual will also be responsible for operating LC-MS instruments (QQQ and HRMS) with minimal direction. Do you have experience in mass spectrometry while doing enzyme related work? This role may be perfect for you! | 3/27/2024 |
| 3002 | Akouos Boston, MA Associate Scientist, Early Preclinical Development - Inner Ear Biology Bachelor's Degree. Exp: 0+ years |
The Early Preclinical Development (EPD) Team is seeking an Associate Scientist with experience in inner ear histology to support discovery and IND-enabling animal studies. The ideal candidate will have experience in histologic techniques specific to the inner ear, such as microdissection of the mouse and non-human primate (NHP) inner ear tissues into discrete anatomical regions, and further processing of these tissues using various histologic techniques, in addition to imaging, analysis, and preparation of data for presentation. Cross-functional work may be required to advance Company goals. The successful candidate will be self-motivated and creative, with a desire to succeed at the highest level in a highly collaborative and fast-paced environment. | 3/27/2024 |
| 3003 | Alexion Pharmaceuticals New Haven, CT Associate Scientist II, Downstream Process Development MS degree in Biochemistry, Chemistry, Chemical Engineering or related discipline from an accredited university. Exp: 0+ years |
The Associate Scientist II is responsible for performing assigned experimental tasks to support the development and optimization of manufacturing processes for Alexion’s biotherapeutic candidates. The Associate Scientist II will work routinely in collaboration with other members of Biologics Process Development, Technology Transfer and Analytical Sciences, including all other groups in Product Development and Clinical Supply. | 3/27/2024 |
| 3004 | Alexion Pharmaceuticals New Haven, CT Associate Scientist II, Pilot Plant Operations MS. Exp: 1+ years |
The Associate Scientist II will perform assigned tasks to support the operational scale up of Pilot-scale manufacturing processes for Alexion’s bio-therapeutic candidates. Work routinely in collaboration with other members of Process Development and other groups in Product Development and Clinical Supply organization. | 3/27/2024 |
| 3005 | Ampac Analytical Rancho Cordova, CA Automation Engineer II Master's Degree in Engineering or Computer Science. Exp: 0-2 years |
Mid-level Automation Engineer will be responsible for PLC Programming, Citect HMI Development, and cGMP documentation development and execution. Additional responsibilities will include developing, testing, and maintaining custom software applications to solve unique problems in a manufacturing environment. Execute small internal control system projects, manage larger vendor supported control system projects. Coordinate and advise process engineering on control system requirements. Engineer must be able to perform industrial field work which may involve some lifting, use of ladders, and stairs. Works under general supervision. | 3/28/2024 |
| 3006 | Ardelyx Fremont, CA QA Specialist III (CSV) Bachelor’s degree in a technical discipline, science /engineering discipline preferred but not required equivalent experience may be considered. Exp: 1-7 years |
We are seeking a highly skilled and detail-oriented QA Computer System Specialist to join our team. The ideal candidate will be responsible for overseeing the quality assurance for all GxP computer systems within our organization. The person in this role will work with the functional teams to ensure that all GxP regulated systems are purchased, audited, installed and maintained according to industry best practices (e.g. GAMP5) and regulatory requirements (e.g. 21CFR Part 11 and relevant FDA Guidance). The position will also support plan and organize QA activities for computer system validation projects. Specific duties of this role include, but are not limited to, overseeing and approving validation- related documents, conducting risk assessments, determining which elements of projects should be validated, assessing and/or coordinating impact of proposed changes to computerized systems, and support activities to prepare for inspections (both external and internal) related to computer system validation. The candidate will also be responsible for maintaining GxP computer systems in a validated state in addition to support designing work processes for users and administrators of these systems. In addition, this position will involve interacting with regulatory agencies and corporate partners during inspections and audits and may require travel to audit computerized system vendors off-site. The incumbent will also develop and implement strategies to ensure compliance with CSV requirements and consistent application of relevant policies and processes. | 3/29/2024 |
| 3007 | Arrowhead Pharmaceuticals Verona, WI Associate Manufacturing Scientist I (2nd shift) BS or MS in chemistry, biochemistry, engineering, or related scientific field. Exp: Entry level to 3 years |
The Associate Manufacturing Scientist I (second shift) supports the production of drug substances and drug products. Their responsibility will focus on the preparation of solutions and reagents by following standard protocols. This technically focused second shift position supports lab work, helps solve problems, and effectively communicates with colleagues. | 3/29/2024 |
| 3008 | Arrowhead Pharmaceuticals Verona, WI Associate Scientist, CMC Process Development BS or MS in chemistry or biochemistry with an excellent understanding of organic and analytical chemistry. Exp: 1+ years |
Chemist in the Development Chemistry Group focusing on oligonucleotide synthesis development. This is an ideal position for an individual with an organic or biological chemistry background who has an interest in projects related to novel technology in synthesis and purification of oligonucleotides and bioconjugates. | 3/29/2024 |
| 3009 | Atec Spine Carlsbad, CA Quality Engineer Minimum Bachelor’s degree (BS) from a four-Year College or university in Mechanical, Industrial and Systems, Biomedical, or Manufacturing Engineering. Exp: 1-5 years |
Develop and improve, with an emphasis on implementation, inspection methods, gages, process control techniques, standard operating procedures, inspection plans, test protocols and test reports to ensure safety, reliability and efficacy of new products and processes. | 3/29/2024 |
| 3010 | Atec Spine Carlsbad, CA Validation Engineer Bachelor’s degree from four-year College or university in Engineering, or equivalent experience. Exp: 0-3 years |
Validation Engineering for New Product Development & Sustaining Engineering with a focus on software systems. Under minimal supervision, the Validation Engineer will work closely with QE, R&D, Marketing, Product Development teams, Supply Chain, and Regulatory to bring products to market while ensuring compliance to applicable standards and regulations. | 3/29/2024 |
| 3011 | Aurora Biolabs San Diego, CA Research Associate I Bachelors or Masters in science related field. Exp: 0-1 year |
Aurora Biolabs, LLC is seeking a motivated research associate I in cell and molecular biology, biochemistry or related field in San Diego, CA. The individual will be a critical part of our products development team, development a new line of recombinant protein products for drug discovery and commercial use. This position requires extensive hands-on experience with a broad range of techniques including protein expression and purification, molecular cloning, PCR, mammalian cell, insect cells and bacterial culture, ELISA, as well as in vitro cell-based/immuno-based assays. You will work in an atmosphere that is stimulating, innovative, and customer focused. | 3/29/2024 |
| 3012 | Beam Therapeutics Durham, NC Manufacturing Associate (Multiple Openings) BS, MS a plus, in Life Sciences or Engineering. Exp: 0-5 years |
Beam is expanding our geographical footprint to RTP, NC with the recent announcement of a 100,000 square foot manufacturing facility in addition to our laboratory-based facilities located in Cambridge, MA. We are looking for highly energetic Manufacturing Associates to support start-up and scaling of cGMP manufacturing at our new RTP site. The successful candidates will provide manufacturing, operational & technical experience around commissioning, training, qualification, and start-up. The ideal candidates will have experience in cell or gene therapy, along with demonstrated ability in a GMP environment. They will also possess the ability to successfully interface with multidisciplinary teams and build strong cross-functional relationships in a team environment. | 3/29/2024 |
| 3013 | Beam Therapeutics Durham, NC QC Analyst Bachelor’s degree required, preferably in a chemistry, life science, or related discipline. Exp: 1-3 years |
Beam is seeking a highly motivated and energetic Analyst to join our growing QC analytical team. The Quality Control Analyst will be responsible for performing various analytical methods to evaluate the quality of critical in-process samples to support cGMP manufacturing operations across multiple site programs. This role will also be responsible for daily laboratory operations including reagent receipt and inventory management and equipment maintenance. This position will support deviation initiation and investigations as well as implementation of continuous improvements. The Analyst will support critical analytical method implementation workstreams in support of program start-up and scale up. This role will work closely with team members in Quality Assurance, Manufacturing, MS&T and Analytical Development. The position will report to the Senior QC Manager. The Analyst I is expected to be an on-site resource at Beam’s manufacturing facility in RTP, North Carolina to support project start-up and routine clinical and commercial operations. | 3/29/2024 |
| 3014 | Berkshire Sterile Manufacturing Lee, MA Formulation Associate I Associates Degree in a science-related discipline. Exp: Zero to two (0-2) years’ |
Perform all formulation operations in the area of assignment and support start-up/changeovers/tech transfer activities. This position works under the immediate direction of the Formulation Supervisor and all work is conducted following a high standard of GMP compliance and written SOP and batch records. | 3/29/2024 |
| 3015 | Berkshire Sterile Manufacturing Lee, MA Manufacturing Associate- 2nd Shift Associates Degree. Exp: zero (0) to two (2) or more years |
Perform all production operations in the areas assigned within the facility. Perform production support operations in areas assigned and support start-up, changeovers and tech transfer activities. | 3/29/2024 |
| 3016 | Berkshire Sterile Manufacturing Lee, MA Process Engineer Process Engineer: Bachelor’s degree in Chemical Engineering, Chemistry, Biology, or Pharmaceutical Science. Exp: One (1) to three (3) years |
The Process Engineer will lead tech transfer projects from client or small scale to manufacturing/large scale in a manner that meets safety, quality, and operational performance expectations. The key function of this role will be to deliver effective, safe and efficient manufacturing processes for parenteral drug products. | 3/29/2024 |
| 3017 | Berkshire Sterile Manufacturing Lee, MA Facilities Engineer Bachelors or Master’s engineering degree. Exp: Up to two (2) years |
The Facilities Engineer will supply engineering expertise to support and continually improve mechanical systems at BSM within the requirements of relevant regulations, cGxPs and the BSM Quality Management System. The Facilities Engineer will perform all work under the supervision and direction of the Senior Engineering Manager. | 3/29/2024 |
| 3018 | BioLife Solutions Bothell, WA Aseptic Technician I Bachelor’s degree; or Associate degree / Biotech cert. Exp: 1 year |
The Aseptic Technician is a core team member of the manufacturing team. The Aseptic Technician is responsible for daily production including environmental monitoring, formulating, and filling of aseptic GMP manufactured products according to batch records and SOPs. This position is for an experienced manufacturing professional with knowledge of GMP, aseptic technique, and problem-solving skills. This position provides an opportunity to solve challenges in a fast-growing industry. BioLife is a fast-growing company that is the leading cell preservation specialist within the fields of biotechnology and pharmaceuticals. This position allows for exposure to many department’s ways of working and opportunities for cross functional projects. Allows for insight into the world of biotechnology.The Aseptic Technician is a core team member of the manufacturing team. The Aseptic Technician is responsible for daily production including environmental monitoring, formulating, and filling of aseptic GMP manufactured products according to batch records and SOPs. This position is for an experienced manufacturing professional with knowledge of GMP, aseptic technique, and problem-solving skills. This position provides an opportunity to solve challenges in a fast-growing industry. BioLife is a fast-growing company that is the leading cell preservation specialist within the fields of biotechnology and pharmaceuticals. This position allows for exposure to many department’s ways of working and opportunities for cross functional projects. Allows for insight into the world of biotechnology. | 3/29/2024 |
| 3019 | BioLife Solutions Indianapolis, IN Aseptic Technician I Minimum: Two years of college-level biological coursework, i.e. in Chemistry, Biology, Physics, etc.Minimum: Two years of college-level biological cou Exp: Entry-level |
Daily production including environmental monitoring, formulating, and filling of aseptic GMP manufactured products according to batch records and SOPs. This position is entry level and an effective way to get started in a fast-growing company that is the leading cell preservation specialist within the fields of biotechnology and pharmaceuticals. This position allows for exposure to many department’s ways of working and opportunities for cross functional projects. Allows for insight into the world of biotechnology. | 3/29/2024 |
| 3020 | BioLife Solutions Bothell, WA Aseptic Technician II Bachelor’s degree. Exp: 1 year |
The Aseptic Technician is a core team member of the manufacturing team. The Aseptic Technician is responsible for daily production including environmental monitoring, formulating, and filling of aseptic GMP manufactured products according to batch records and SOPs. This position is for an experienced manufacturing professional with knowledge of GMP, aseptic technique, and problem-solving skills. This position provides an opportunity to solve challenges in a fast-growing industry. BioLife is a fast-growing company that is the leading cell preservation specialist within the fields of biotechnology and pharmaceuticals. This position allows for exposure to many department’s ways of working and opportunities for cross functional projects. Allows for insight into the world of biotechnology. | 3/29/2024 |
| 3021 | BioLife Solutions Bothell, WA Quality Specialist I Bachelor’s degree. Exp: 0-2 years |
The Quality Assurance Specialist is a core team member of the Quality department. The Quality Assurance Specialist ensures the Quality Management System (QMS) programs flow in a timely and accurate fashion, and that the programs are in compliance with all business requirements. Quality Assurance is a trusted partner to other departments and builds strong relationships both internally and externally. This position must demonstrate abilities to work cross-functionally throughout the company with superior communication skills. A motivated self- starter and attention to detail finisher is key to the core role of Quality Assurance, ensuring that all procedures are processed in a timely fashion and right the first time. | 3/29/2024 |
| 3022 | Biomerics Salt Lake City, UT Design Transfer Engineer I A bachelor’s degree in engineering or a related field (mechanical, biomedical, chemical) is required. (Required). Exp: 1+ years |
The Design Transfer Engineer I will be responsible for designing and manufacturing transfer of class II medical and surgical devices in a dynamic, customer-focused organization. The Design Transfer Engineer I will be expected to work with customers to understand product and process specifications, develop and transfer manufacturing processes, and build and test devices to those specifications. All activities will be expected to be documented according to design control requirements in a design history file (DHF). The Design Transfer Engineer I will support verification, validation, and regulatory submissions of these devices, then lead the transfer of the products to production and ensure a smooth transition to the production engineering team. The Design Transfer Engineer I will work within the constraints of budget, schedule, and scope while managing risk and ensuring adherence to established processes & regulations. The Design Transfer Engineer I may be an individual contributor and participate as part of a small cross-functional team comprising engineering, operations, and quality members to provide process and manufacturability input to designs throughout the product development process. | 3/29/2024 |
| 3023 | Biomerics Brooklyn Park, MN Industrial Engineer A bachelor’s degree in industrial engineering or an engineering degree is required. Exp: 1+ years |
This position will play an integral role at BAC by driving and implementing continuous improvement throughout the business. The IE works cross-functionally across the plant to eliminate waste and improve product, material, and information flow. | 3/29/2024 |
| 3024 | Biotium Fremont, CA CHEMISTRY TECHNICIAN I (CHEMISTRY) B.S. or M.S. degree in Chemistry. Exp: 1+ years |
Under the direct supervision from a senior chemist, perform chemical purifications using chromatography including preparative HPLC or gravity chromatography; carry out chemical synthesis using standard protocols; carry out chemical analyses using modern instruments including analytical HPLC, LC-MS, TLC, UV/Vis and fluorescence spectrophotometry. | 3/29/2024 |
| 3025 | Biotium Fremont, CA RESEARCH ASSOCIATE I, BIOSCIENCE B.S. in Biology, Molecular Biology, Biochemistry or a related field. Exp: 1+ years |
Under direct supervision from the VP of Research and Development, perform synthesis, purification, and characterization of antibody/biomolecule conjugates of fluorescent dyes, fluorescent proteins, tandem dyes, enzyme reporters, and polymeric scaffolds. Research and development leading to commercialization of bioconjugates for research applications. The successful candidate will possess a strong background in chemistry and bioconjugation chemistry and have experience performing bioconjugation reactions, protein purification, and requisite analytical techniques. | 3/29/2024 |
| 3026 | Visby Medical San Jose, CA Product Transfer Engineer I Bachelor’s degree in engineering or related field. Exp: 1-2 years |
The Product Transfer Engineer plays a vital role in transitioning products from design and development to full-scale production. The individual will also be responsible for root cause investigations under the guidance of senior team members to ensure smooth operations. | 3/29/2024 |
| 3027 | Boston Analytical Salem, NH Analytical Chemist I, Raw Materials Qualification include a Bachelor’s degree in Chemistry or a related discipline is required. Exp: 0-2 years |
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties include performing analysis of Raw Materials using AA, UV-Vis, and Wet Chemical Analysis according to USP/EP methods. | 3/29/2024 |
| 3028 | Boston Analytical Salem, NH Microbiologist QC I - Framingham Qualifications include a BA or BS degree in Microbiology or related science discipline. Exp: 0-2 years |
The QC Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. Location: Framingham, MA | 3/29/2024 |
| 3029 | Boston Institute of Biotechnology Southborough, MA Research Associate – Downstream Process Development BS degrees in biology, biochemistry, biomedical/biochemical engineering, or related fields. Exp: ≤1 year |
A Research Associate I is an entry level position for Bachelor’s degree with no prior experience and reports to a scientist level or above on relevant projects. The individual is responsible for routinely setting up, operating, and maintaining the downstream lab equipment under direct supervision. | 3/29/2024 |
| 3030 | Boston Institute of Biotechnology Southborough, MA Assoc. Scientist – Downstream Process Development MS degree in biology, biochemistry, biomedical/biochemical engineering, or related fields. Exp: ≥1 year |
The Associate Scientist is responsible for development and execution of downstream related projects with moderate direct supervision. The individual reports to a more senior scientist level or above on relevant projects. The individual will provide expertise in the development and optimization of downstream processes. | 3/29/2024 |
| 3031 | KCAS Bioanalytical Olathe, KS Associate Scientist - Pharma LC-MS/MS Bachelor’s degree in Chemistry, Biochemistry, or related field. Exp: 1-3 years |
When you work as an Associate Scientist on the Pharma LC-MS/MS team, you get to further our mission by being a contributing scientist on studies, with the ability to carry out all aspects from study setup and development, through reporting with some assistance. You will need to utilize a strong base in scientific principles/theory to assess data integrity and troubleshooting, while independently completing experiments. | 3/18/2024 |
| 3032 | KCAS Bioanalytical Olathe, KS Analyst II - Pharma LC-MS/MS BS/BA degree in Chemistry, Biochemistry, or other life science field. Exp: one year |
When you work as an Analyst II in the Pharmaceutical Liquid Chromatography Mass Spectrometry (LC-MS/MS) lab at KCAS, you get to further our mission by working under senior Pharma LC-MS/MS scientists to contribute to the success of our clients. | 3/18/2024 |
| 3033 | Latitude Pharmaceuticals San Diego, CA QC Associate Minimum BS degree in Chemistry or chemistry-related field. Exp: 1+ years |
LATITUDE Pharmaceuticals Inc., a San Diego-based contract drug developer and manufacturer, is seeking a Quality Control Associate to be a key member of the QC group. A successful candidate should have some experience in drug product manufacturing and analytical testing techniques under GMP. This is a full-time position and will report to the Director of Quality. The position will be located in San Diego, California. | 3/18/2024 |
| 3034 | Lodo Therapeutics Cambridge, MA Operations Engineer 1, DNA Synthesis (Weekend Shift) at Ginkgo Bioworks Inc. Bachelor's degree in biology, biochemistry or biomedical engineering. Exp: 1+ years |
We're seeking a DNA Synthesis Operations Engineer to join our team to execute, improve, and scale our state-of-the-art manufacturing process flows. You’ll apply molecular biology protocols to perform efficient and high-quality lab-work in a fast-paced setting. You will use your excellent communication skills and flexibility to work effectively within a diverse team. You’ll display your breadth by leveraging the technology, software, automation, and instrumentation acumen required by our detailed processes flows. Please note that this position is to be filled at our Cambridge, MA location and will cover a four day, 10 hour per day work schedule (Thursday to Sunday - 10AM to 8PM). | 3/18/2024 |
| 3035 | Regulus Therapeutics San Diego, CA Temp/Hire: Research Associate – Senior Research Associate, Drug Discovery Biology MS in Biology or related discipline. Exp: 1+ years |
We are excited to invite a dedicated and driven individual to join our Research Biology team. This role is designed for a qualified candidate who seeks the opportunity to evolve as a drug discovery scientist, with a specific focus on microRNA biology, oligonucleotide therapeutics, and CNS-related diseases. The successful candidate will serve as a hands-on cell and molecular biologist, contributing valuable research experience and skills to the organization. The role encompasses a spectrum of drug discovery efforts, spanning early-stage target identification to advanced IND-related activities. The ideal applicant should possess direct experience in various molecular techniques, a robust understanding of cell biology, and excellent organizational and presentation skills. This position presents an exciting prospect to contribute to the exploration of innovative oligonucleotide therapeutics addressing areas of high unmet medical need. | 3/20/2024 |
| 3036 | AGC Biologics Seattle, WA Downstream Manufacturing Associate I/III Bachelor’s degree or Biotech certificate, quality systems regulations (cGMP) knowledge. Exp: 1+ years |
The role of the Manufacturing Associate is to act as a controller, providing essential duties to support the respective production suite, Supervisor and Manager. On a daily basis, the Manufacturing Associate is expected to have a full understanding of the schedule and required tasks; promoting adequate assessment and response of any production demands. The Manufacturing Support Technician will be responsible for fulfillment of immediate requests from the Manufacturing Operations departments including, but not limited to, assembly preparation, washing parts, autoclaving of parts, kitting parts for delivery and facility sanitizations. The deadline for applications is the 31st of March. | 3/20/2024 |
| 3037 | AGC Biologics Boulder, CO Quality Assurance Associate I-III (In Plant Operations) Bachelor’s degree in Biology, Chemistry or other relevant science/engineering discipline. Exp: Associate II – 0 - 2 years |
The Quality Assurance Associate I- III (In Plant Operations) is responsible for providing (24/7/365) Quality support to the activities listed below at the Boulder, CO site. SCHEDULE: 2-2-3 Blue Days | 3/20/2024 |
| 3038 | AGC Biologics Seattle, WA Quality Control Associate I BS/BA degree. Exp: 1-3 years |
The Quality Control Associate I will perform QC analysis and document activities according to SOPs following good manufacturing processes (GMP). This individual will also demonstrate the ability to learn QC methods, procedures and systems. | 3/20/2024 |
| 3039 | AGC Biologics Seattle, WA Upstream Manufacturing Associate I/III Bachelor’s degree or Biotech certificate, quality systems regulations (cGMP) knowledge. Exp: 1 year |
The role of the Manufacturing Associate is to act as a controller, providing essential duties to support the respective production suite, Supervisor and Manager. On a daily basis, the Manufacturing Associate is expected to have a full understanding of the schedule and required tasks; promoting adequate assessment and response of any production demands. The Manufacturing Support Associate will be responsible for fulfillment of immediate requests from the Manufacturing Operations departments including, but not limited to, assembly preparation, washing parts, autoclaving of parts, kitting parts for delivery and facility sanitizations. | 3/20/2024 |
| 3040 | AGC Biologics Seattle, WA; Boulder & Longmont, CO, US Upstream Process Development Associate I A.A./B.S. in a life science or engineering. Exp: 1-3 years |
This is a Development Associate I position in the Upstream Process Development group. Primary responsibility will be to support mammalian cell culture processes used for the manufacture of therapeutic recombinant proteins. The successful candidate will be responsible for supporting shake flask and bioreactor experiments, sampling, inoculating, feeding & harvesting bioreactors. Under general supervision, this person carries out routine to moderately complex experiments or procedures. The deadline for applications is the 31st of March. | 3/20/2024 |
| 3041 | Aptitude Medical System Santa Barbara, CA Research Associate Bachelor’s degree or Master’s degree in a relevant discipline. Exp: Entry-level |
We are seeking to hire multiple capable and driven entry-level Research Associates to join our tight-knit research and development team. In this position, you will be working closely with a cross-functional team of mission-driven scientists and engineers to drive the invention and development of novel diagnostic products. | 3/21/2024 |
| 3042 | Aura Biosciences Brighton, MA Sr. Associate Scientist, Upstream Degree in biochemical engineering, biological sciences, biochemistry or related discipline. M.S. Exp: 1+ years |
Reporting to the Upstream Process Development Lead, the (Sr) Associate Scientist will be responsible for the development of upstream production processes and the production of material for routine in-house development use. This includes all assays associated with cell culture production. The incumbent will also participate in the transfer of the upstream process to support biopharmaceutical product development at Contract Manufacturing Organizations (CMOs). The scientist will interact with the in-house team and the CRO/CMO to ensure timely progress in technology development, documentation, and manufacturing readiness. | 3/21/2024 |
| 3043 | Bio-Concept Laboratories Westborough, MA Entry Level Scientist 1 - 2nd Shift Bachelor’s degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience. Exp: Entry-level |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. Schedule: Sunday - Thursday 4:00 pm - 12:30 am What you’ll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate equipment Maintain detailed and organized documentation on all laboratory work | 3/21/2024 |
| 3044 | Bio-Concept Laboratories Sheridan, WY Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. What you’ll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate equipment Maintain detailed and organized documentation on all laboratory workJoin us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 3/21/2024 |
| 3045 | Bio-Concept Laboratories Westborough, MA Entry Level - Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. Schedule: Sunday - Thursday 8 am - 4:30 pm What you’ll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate equipment Maintain detailed and organized documentation on all laboratory work | 3/21/2024 |
| 3046 | Bio-Concept Laboratories Mt. Juliet, TN Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. What you’ll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate equipment Maintain detailed and organized documentation on all laboratory wor | 3/21/2024 |
| 3047 | Bio-Concept Laboratories Mansfield, MA Scientist 1 -Metals- Entry Level Bachelor’s degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience. Exp: 1+ years |
Find your place at Pace® Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. Schedule: Monday - Friday 3 pm - 11:30 pm What you’ll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate equipment Maintain detailed and organized documentation on all laboratory work | 3/21/2024 |
| 3048 | Bio-Concept Laboratories Mansfield, MA Scientist 1 - Metals - Early Mornings Bachelor’s degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. Schedule: Monday - Friday 5 am - 1:30 pm What you’ll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate equipment Maintain detailed and organized documentation on all laboratory work | 3/21/2024 |
| 3049 | Bio-Concept Laboratories Greensburg, PA Environmental Scientist - Entry Level Bachelor’s degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience. Exp: Entry-level |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. What you’ll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate equipment Maintain detailed and organized documentation on all laboratory work | 3/21/2024 |
| 3050 | Biofactura Frederick, MD Quality Control Analyst Bachelor’s degree required. Exp: 1+ years |
The QC Analyst will support the establishment and growth of BioFactura’s QC department. Responsibilities include, but are not limited to, performing QC testing of DS/DP release and stability samples in support of BioFactura programs; ensuring compliance with established regulatory practices and standards; working with Analytical Development (AD) on the transfer of qualified assays to QC; assisting with assay validation activities; and authoring and review of SOPs, protocols, and reports. | 3/22/2024 |
| 3051 | BioRestorative Therapies Melville, NY cGMP Bio -Manufacturing Engineer MSc degree in cell biology or similar discipline. Exp: 1 to 6 years |
BioRestorative Therapies, Melville, NY is recruiting for a cGMP bio-manufacturing engineer. This role provides outstanding opportunities for talented self-motivated individuals, ideally with experience in (stem) cell biology, immunology, and/or molecular biology, who can contribute to our ongoing efforts to generate clinical grade cell-based therapeutics. We are most interested in connecting with qualified individuals who aspire to support the development of therapeutics and/or life science products and tools to support research endeavors. | 3/22/2024 |
| 3052 | ChemPacific Baltimore, MD Chemist Master’s degree in Chemistry or Organic Chemistry. Exp: one year |
Perform multi-step organic synthesis in solution and/or solid support: Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps such as extraction, recrystallization, silica gel column chromatography and LC/MS purification; perform cGMP synthesis of pharmaceutical ingredients; and perform process development and scale-up for kilogram quantities; and clearly record and communicate results and challenges to coworkers/supervisor. Equipments and tolls used included NMR, UV, MS and IR, Reactor (from 50ml to 221 to 10000l), vacuum pump, water aspirator, condenser, rotavap, voltage transformer, chromatography columns, TLC monitor, lyophilizer, separation funnel and addition funnel. Please send your resume to xtan@chempacific.com | 3/22/2024 |
| 3053 | CRISPR Therapeutics Boston, MA Research Associate II, in vivo Oligonucleotide Chemistry MS degree in Chemistry, Chemical Engineering, Biochemistry, Bioengineering, Pharmaceutical Sciences or related field. Exp: 1+ years |
CRISPR Therapeutics is seeking a highly motivated Research Associate to join our In Vivo Technical Operations department in Boston, Massachusetts. The incumbent will be responsible for the oligonucleotide synthesis, purification, desalting, and analysis to support the process development of guide RNA production in various scales. This position will also support therapeutic programs in multiple disease areas in R&D department. Prior experience in oligonucleotide synthesis, purification, and characterization is desired | 3/22/2024 |
| 3054 | GenEdit South San Francisco, CA Lab Technician, Chemistry (Part Time) Associate degree (or) bachelor’s degree in any science field or equivalent experience. If the candidate is willing to be promoted to RA I, the positio Exp: RA I: 0-2 years |
GenEdit is seeking a highly self-motivated Lab Technician to provide support to the Chemistry team. The Lab Technician will be responsible for assisting the Medicinal Chemistry Team in cataloging and organizing the inventory of synthesized polymers, alongside routine lab maintenance and aliquot distribution. They will have a key role in chronicling the various modes of organic, polymer, and analytical chemistry performed at GenEdit. A successful candidate will be collaborative, resourceful, and enthusiastic to work in a team environment. This candidate will report to the Principal Scientist in the Chemistry Department and communicate with all interdisciplinary groups like formulation, in vitro and in vivo teams. This position may convert into a full time Research Associate (RA I) in a year subject to candidate’s performance and the requirement by the Chemistry department. Upon promotion to RA, the candidate will be working in organic synthesis of bio-synthetic polymer, macromolecule and/or complex organic molecule characterization utilizing various separation and detection techniques in support of research, regulatory and business efforts. They will be responsible for synthesis of novel polymer molecules, assist with developing, implementing, and validating analytical methods to characterize novel polymers for gene delivery nanoparticles. This position will also participate in the development and routine performance of polymer characterization assays for identity and purity, preparation of certificates of analysis (COA), and preparation of standard operating procedure (SOP). Additional duties and responsibilities may be required as needed. | 3/22/2024 |
| 3055 | Immucor Norcross, GA MQA Technician II Associate’ Degree (AA) or equivalent from a two-year college or technical school; Bachelor’ degree is highly preferred. Exp: six months to one year |
We are seeking an experienced Manufacturing Quality Assurance (MQA) Technician II to join our team. Our company is a growing medical technology firm that offers challenging positions, opportunities for professional growth, and competitive benefit packages to all employees. Our company is founded on and guided by our corporate mission and values: respect, integrity, teamwork, and achievement. If you have the necessary skills and experience to excel in this position, we want to hear from you! | 3/22/2024 |
| 3056 | Indivior Raleigh, NC Controls Engineer Bachelor of Science in Engineering or related field. Exp: 1+ years |
The Controls Engineer is a technical resource to the engineering, maintenance, validation and operations departments, to meet all regulatory and Company specific policy requirements and objectives, and to improve plant efficiency, capacity, capability and modernization. This person is responsible for the research, development, design, layout, building, testing, troubleshooting, repairs and improvement of all manufacturing control systems, including the Building Management System (BMS), HVAC, and Utility Control Systems. The position is also responsible for implementing improvements to increase equipment efficiency and prevent obsolescence, as well as ensuring the validated state of all applicable equipment, systems and facilities. This position will maintain compliance with all company standard operating procedures (SOPs) and applicable cGMP, OSHA, EPA, and local government regulations. | 3/22/2024 |
| 3057 | Indivior Raleigh, NC Environmental Monitoring Technician II Bachelor of Science degree in a life science or equivalent. Exp: 1-3 yrs |
This position reports to the EM Supervisor for the functional area to which they are assigned and has no direct reports. This individual holding the position of EM Technician II shall be responsible for performing routine environmental monitoring to assess the viable and nonviable particulate levels within classified manufacturing rooms, critical utilities and controlled environments. | 3/22/2024 |
| 3058 | Lampire Biological Labs Everett, PA Laboratory Technician BS in relevant field. Exp: 1-2 years |
Job Description: To facilitate daily operations at the Coopersburg Laboratory by supporting the whole blood, plasma/serum, anticoagulant, brokered and abattoir departments as necessary. | 3/22/2024 |
| 3059 | NeuMoDx Molecular Ann Arbor, MI MANUFACTURING SPECIALIST, REAGENT College Degree (BS/BA) in science or chemistry field. Exp: 1 year |
Manufacturing Specialists are required to have a strong knowledge of manufacturing methods and techniques, process development experience, work flow understanding, ability to understand formulations and follow recipes and testing protocols for any in-process Quality checks • In this position, Manufacturing Specialists, will maintain manufacturing equipment, create work instructions, train others, often be asked to contribute to or lead projects, be cross functionally trained to work in several areas as needed. • This role requires a self-starter, ability to work independently, understanding of departmental goals-working as a team to achieve those goals within set timelines. | 3/22/2024 |
| 3060 | Physical Sciences Andover, MA Chemical Engineer BS or MS degree in Chemical Engineering, Chemistry or Materials Science. Exp: 0 to 2 years’ |
Physical Sciences Inc., located just north of Boston in Andover, has a career opportunity for a Chemical Engineer with a strong background in reaction kinetics, heat and mass transfer, and separations. We are seeking an applicant who can assist with developing and scaling-up materials production from laboratory/batch processes to pilot-scale/continuous processes. The applicant we seek would benefit from material development, purification and characterization experience. We are looking for a strong worker, who can safely and effectively execute on their ideas as a member of a team and sometimes as an individual contributor. This Chemical Engineer will be asked to work on innovative programs, in areas such as atmospheric water harvesting, continuous process development, and waste conversion to high performance materials. Experience with wet chemistry laboratory procedures and related analytical techniques is essential. Hands on experience with hardware assembly for chemical processes is preferred. Working knowledge of analytical laboratory techniques (e.g. GC-MS, FTIR, NMR, DSC, TGA, tensile testing) and chemical engineering software packages (e.g. Comsol) is highly desirable. | 3/22/2024 |
| 3061 | Physical Sciences Andover, MA Optical Engineer Bachelor’s degree in optical or mechanical engineering, physics or equivalent. Exp: 1+ years |
Physical Sciences Inc., a 100% Employee-Owned company located just north of Boston in Andover, seeks an Optical Engineer with professional experience to support development of emerging optical technologies. The candidate will support optical systems design, construction, and testing needs for illuminators, projectors, integrated spectrometers and/or metasurfaces. A strong basic understanding of optical system layout and construction is sought. | 3/22/2024 |
| 3062 | Physical Sciences Andover, MA Experimental Physicist Bachelor or Masters degree in Physics, Applied Physics, Optics, or Related Discipline. Exp: 0-5 years |
Physical Sciences Inc., located just north of Boston in Andover, MA, seeks an experimental physicist with experience in laser-based tools related to applications such as atom sensing, integrated photonics, or optical materials development. The candidate will join teams at PSI and contribute to invention, demonstration, and deployment of technology platforms targeting these application areas. The ideal candidate will have a bachelor’s or master’s degree in physics or related disciplines and should be interested in applied research and development with strong experimental, hardware, and leadership skills. | 3/22/2024 |
| 3063 | The Ritedose Corporation Columbia, SC Microbiologist Technician Technical degree in life science or related field. Exp: 1+ years |
The Microbiologist Technician is responsible for all duties related to performing environmental monitoring, personnel monitoring. Other responsibilities include data entry, data review, ensuring calibration of equipment, maintaining and ordering inventory of laboratory supplies, and maintaining the Microbiology laboratory by ensuring its cleanliness and order. | 3/22/2024 |
| 3064 | Sedia Biosciences Beaverton, OR Production Technician I High School diploma, Training Certificate, or Associates degree (technical field preferred). Exp: Entry level |
Production Technicians at Sedia will be responsible for the production of Sedia’s products. This includes the formulation of reagents, application of reagents to various materials, dispensing of testing reagents into vials, tubes, or bottles, capping and labeling of components and assembly of components into finished test kits. Technicians will be working with standard laboratory equipment as well as automated and semi-automated production equipment. | 3/22/2024 |
| 3065 | Sedia Biosciences Beaverton, OR QC Technician I High School diploma, Training Certificate, or Associates degree (technical field preferred). Exp: Entry-level |
This position works under direct supervision to perform Quality Control functions including the inspection and testing or raw materials, components, and finished products in a medical diagnostic manufacturing environment. Works in compliance with the Quality Management System and under applicable quality standards such as ISO-13485 and CFR 21 part 820 cGMPs. | 3/22/2024 |
| 3066 | Acceleron Pharma Rahway, NJ Specialist, Process Engineer - Oral Solid Dosage, Clinical Manufacturing Bachelor’s degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field. Master’s degree in Chemical Engineering, Ch Exp: BS: 1 year; MS: 0 years |
The Process Engineer role at the Specialist level will serve as a leader in the FLEx Oral Solid Dosage GMP Clinical Manufacturing facility. This role will support formulation and process development, scale-up activities, quality investigations, change management and authoring GMP standard operating procedures and protocols in support of oral solid dosage clinical drug product operations. This individual will collaborate closely with the formulation scientists, engineers, quality representatives, and other team members to ensure the quality of the clinical supplies, the scientific rigor of the processes, and ultimately to enable the flexibility and speed of our Company's pipeline. The role is based in New Jersey and reports to the Oral Solid Dosage Process Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply. | 3/22/2024 |
| 3067 | Acceleron Pharma Rahway, NJ Specialist, Process Engineering Bachelor’s degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field. Master’s degree in Chemical Engineering, Ch Exp: BS: 1 year; MS: 0 years |
The Process Engineer role at the Specialist level will serve as a leader in the FLEx Sterile GMP Clinical Manufacturing facility. As the facility is nearing the completion of its construction, the selected candidate will contribute to equipment and facility commissioning/qualification, regulatory certification, as well as other workstreams’ critical activities to enable facility startup and operational readiness. To support these business-critical activities, night and weekend work may be required. Once the facility is operational, this role will support formulation and process development, scale-up activities, quality investigations, change management and authoring GMP standard operating procedures and protocols in support of sterile clinical drug product operations. This individual will collaborate closely with the formulation scientists, engineers, quality representatives, and other team members to ensure the quality of the clinical supplies, the scientific rigor of the processes, and ultimately to enable the flexibility and speed of our Company's pipeline. The role is based in New Jersey and reports to the Sterile Process Engineering Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply. | 3/22/2024 |
| 3068 | Acceleron Pharma Rahway, NJ Specialist, Analytical Research and Development Advanced and relevant industry experience for applicants with a Bachelor of Science degree, or beginner, relevant industry experience for applicants w Exp: 1+ years |
The Small Molecule Analytical Research and Development group has an opening for a Specialist based in Rahway, NJ. Join us and experience our culture first-hand - one of strong ethics & integrity, diversified experiences, exceptional science, and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. In your role as Specialist, you will be part of a team of Specialists working on cross-functional scientific teams to enable development of novel small molecule, peptide, and oligonucleotide drug development through laboratory-based analytical characterization of our raw materials including excipients and package components. | 3/22/2024 |
| 3069 | Acceleron Pharma Rahway, NJ Specialist, Process Engineer - Oral Solid Dosage, Clinical Manufacturing Bachelor’s degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field. Master’s degree in Chemical Engineering, Ch Exp: BS: 1 year; MS: 0 years |
The Process Engineer role at the Specialist level will serve as a leader in the FLEx Oral Solid Dosage GMP Clinical Manufacturing facility. This role will support formulation and process development, scale-up activities, quality investigations, change management and authoring GMP standard operating procedures and protocols in support of oral solid dosage clinical drug product operations. This individual will collaborate closely with the formulation scientists, engineers, quality representatives, and other team members to ensure the quality of the clinical supplies, the scientific rigor of the processes, and ultimately to enable the flexibility and speed of our Company's pipeline. The role is based in New Jersey and reports to the Oral Solid Dosage Process Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply. | 3/22/2024 |
| 3070 | Acceleron Pharma Rahway, NJ Specialist, Quality Assurance (Hybrid) Bachelor degree (B.S.) in an appropriate Science or Engineering discipline (engineering, chemistry, biology, biochemistry, microbiology). Exp: 1+ years |
The Rahway based Specialist, Global Development Quality Operations - API, is responsible for review and approval of documentation to support Good Manufacturing Practice (GMP) clinical supply API manufacture, testing, release and maintenance in support of our company's clinical supply programs. This person will also review and approve documentation accompanying the disposition of API materials (including new modalities) to ensure conformance to appropriate regulatory and company requirements for clinical supply manufacture and/or regulatory inspections. Performs audits of batch documentation, data, information, procedures, equipment and systems, and/or facilities to ensure the compliance with Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMPs) and other applicable worldwide regulations and our Company procedures. The Specialist will become knowledgeable in regulatory requirements, cGMPs and our company's procedures to assure API (including new modalities) manufacturing and testing is in compliance and will gain competency in their responsibilities. | 3/22/2024 |
| 3071 | Tris Pharma Monmouth Junction, NJ Associate QC Analytical Chemist Bachelors in Chemistry or related scientific field. Exp: 0-3 years |
We have an immediate opening in our Monmouth Junction, NJ QC Lab for an (Associate) QC Analytical Chemist. This is an entry level scientific position and we will train qualified candidates who meet listed requirements. Recent college graduates are welcome to apply. The (Associate) Quality Control (QC) Analytical Chemist performs analytical testing of raw materials, packaging components, in-process (IP), finished product (FP), and/or stability samples (ST). She/he is also responsible for following Analytical Methods, current Good Manufacturing Practices (cGMPs), Protocols, Standard Operating Procedures (SOPs) and company policies. | 3/11/2024 |
| 3072 | Turn Biotechnologies Mountain View, CA Research Associate - Synthetic Chemistry, CMC BS/MS in organic/synthetic chemistry or related discipline. Exp: 1-3 years |
Turn Biotechnologies is seeking an excellent Research Associate with strong knowledge and hands on experience in synthetic/organic chemistry to work in our CMC team. The ideal candidate should have experience in synthesizing, purifying and characterizing small molecules, in particular lipids. Additionally, experience in polymer chemistry is a plus. | 3/11/2024 |
| 3073 | Vor Biopharma Cambridge, MA GMP Operations Associate BS in Biology or related field. Exp: 1 - 3 years |
Vor Bio is seeking a GMP Operations Associate who is an enthusiastic and driven individual to support cGMP manufacturing for clinical phase cell therapy manufacturing facility. The candidate will be responsible for providing assistance in the support area for the manufacturing of Vor’s gene-edited cell therapies and maintaining compliance of cGMPs in manufacturing areas. | 3/15/2024 |
| 3074 | Wright Medical Portage, MI Electrical Design Engineer Bachelor's degree in EE or related discipline required. Exp: 0+ years |
This role is on the Electrical Engineering team at Stryker Medical division's Acute Care business unit. We primarily work with patient handling and patient care equipment within the hospital space such as stretchers, hospital beds, and support surfaces. This role falls under the team addressing the high-acuity market, with a focus on products that often come into direct contact with patient. It includes gaining a deep understanding of customer needs through research and partnership with upstream marketing and through direct interactions with customers. Working with a diverse team, you will design, develop, modify, evaluate, and verify electrical components and sub-systems for medical devices. The role includes the full development process from research to product launch. | 3/15/2024 |
| 3075 | Wright Medical Mahwah, NJ Operations Engineer Bachelor’s degree in engineering- Required. Exp: 1 year |
Stryker Orthopedics is seeking to hire an Operations Engineer to support the manufacturing of joint replacement products in Mahwah, New Jersey. As an Operations Engineer with the operations team you will provide manufacturing engineering support and direct projects for assigned cells. | 3/15/2024 |
| 3076 | ZeptoMetrix Raleigh, NC Production Scientist I Bachelor’s degree in Chemistry, Engineering or related field from an accredited higher learning institution. Exp: Up to 2 years |
The Production Scientist I will involve all manufacturing tasks related to the production of the company’s organic products. Responsibilities include manufacturing, handling, and packaging various classes of organic compounds as per standard operating procedures. The incumbent must be a dynamic individual who can multi-task and perform various activities associated with manufacturing operations while adhering to all safety policies and high quality Standard Operating Procedures. This position requires hands on chemistry lab work and will report to the Organic Manufacturing Lead. | 3/15/2024 |
| 3077 | ZeptoMetrix North Charleston, SC Scientist I, Quality Bachelor's degree in Chemistry or related field. Exp: 1 year |
The Quality Control (QC) Scientist is primarily responsible for the quality control of starting materials, in-process materials and the finished goods. The incumbent must be a dynamic individual who can work in a diversified group and able to handle multi-tasks within QC operations. The candidate must possess a good working knowledge of Analytical Chemistry. This position requires hands on chemistry lab work and troubleshoot instruments and solve complex spectroscopic problems. | 3/15/2024 |
| 3078 | Zimmer Biomet Warsaw, IN Development Engineer I Minimum B.S. degree from an ABET accredited school (or global equivalent) in one of the following engineering disciplines: Mechanical Engineering, Mec Exp: 1 - 3 years |
*Please note, this role is a hybrid position, partially onsite in Warsaw, IN and partially remote. You have a key support role with responsibility for new product design, development, and commercialization; and/or to maintain in the market innovative medical device products in order to further Zimmer Biomet’s mission and grow Zimmer Biomet’s market leadership position | 3/15/2024 |
| 3079 | Zimmer Biomet Warsaw, IN Technician College/University courses in Microbiology, Biology, Chemistry, Engineering Mechanics, Medical Technology or other related field preferred. Exp: 0 – 3 years |
Responsible for supporting the daily operations of the laboratory at all Zimmer Biomet Warsaw facilities and for operating and maintaining laboratory equipment for the necessary assigned tasks per area work instructions. May also be responsible for ensuring that equipment calibration and maintenance (preventive and/or corrective) is performed. | 3/15/2024 |
| 3080 | Zimmer Biomet Warsaw, IN Development Engineer I Minimum B.S. degree from an ABET accredited school (or global equivalent) in one of the following engineering disciplines: Mechanical Engineering, Mec Exp: 1-3 years |
*This is a hybrid position, partial remote/partially onsite, in Warsaw, IN. Responsible for the design, development, and processing of patient specific implants and instruments based upon individual patient anatomy or conditions. Work is expected to encompass both the development of new products and maintenance of existing products. Position will lead small scope project as a project leader or portions of larger scope project as a core team member as well as individual patient cases within the Patient Matched Implants (PMI) department. | 3/15/2024 |
| 3081 | Z-Medica Morrisville, NC Associate R&D Engineer, Sustaining Possession of bachelor’s degree in engineering. Exp: One year |
This is an entry level engineering position that will support the sustaining engineering group for the Emergency Medicine product families. However, assignments may include work for other products within the Teleflex portfolio. Experience and background requirements should focus on disposable products. Incumbent organizes and manages multiple projects and ensures projects are completed in a timely manner; Assignments may focus on sustaining engineering assignments providing creative solutions to existing products when problems arise, or modifications are requested. Performs other duties as required or assigned. | 3/15/2024 |
| 3082 | Z-Medica Morrisville, NC Associate R&D Engineer, Sustaining Possession of bachelor’s Degree in Engineering. Exp: One year |
This is an entry level engineering position that will support the sustaining engineering group for the anesthesia products lines. However, assignments may include work for other products within the Teleflex portfolio. Experience and background requirements should focus on disposable products. Incumbent organizes and manages multiple projects and insures projects are completed in a timely manner; Assignments may focus on sustaining engineering assignments providing creative solutions to existing products when problems arise, or modifications are requested. Performs other duties as required or assigned | 3/15/2024 |
| 3083 | Z-Medica Jaffrey, NH Associate Manufacturing Engineer Bachelor's Degree in Polymer/Plastics Engineering or equivalent field required. Exp: 0-2 years |
Results-driven professional is dedicated to constant learning and training. We are looking for an Polymer or Chemical Engineer to join our team. You will be responsible for assisting, planning, designing, and completing projects in extrusion manufacturing utilizing six sigma/lean/DMAIC or like methodologies. The ideal candidate would have experience working with manufacturing equipment and processes to optimize production and increase capacity. Must have equipment acumen, with the ability to be creative and troubleshoot when necessary. Technical aptitude, people-centric, and ability to assist the PTFE and melt extrusion departments. | 3/15/2024 |
| 3084 | Z-Medica Maple Grove, MN Environmental Technician Bachelor’s Degree in Biology, Chemistry, Microbiology or other related science or engineering field. Exp: 0 - 2 years |
Responsible for the environmental/microbial control in the Teleflex manufacturing facilities. Complete planning, coordination and execution of deliverables related to environmental control, microbial control, sterilization qualifications and cleaning/disinfection control of manufacturing areas. | 3/15/2024 |
| 3085 | Z-Medica Maple Grove, MN Microbiologist I Bachelor’s Degree required in a related scientific discipline. Exp: No previous professional experience required. |
This role is responsible for complete execution of deliverables related to microbiology testing, contamination control, cleaning/disinfection validation of manufacturing areas, product release testing, and controlled environment monitoring/certification. This will require review of samples to ensure testing is performed according to provided work instruction. Fulfill microbiology role supporting new product development, production, controlled environments, and sterilization. | 3/15/2024 |
| 3086 | Z-Medica Morrisville, NC Service Engineer Minimum AA/AS/BS or demonstrated equivalent. Exp: 1 year |
This individual is responsible for the troubleshooting, service and repair of VPS products following established procedures and work instructions at the Morrisville, NC Service Center. They will support critical business activities related to servicing VPS capital equipment products focused on the customer experience, continuous improvement and workflow efficiencies This role will collaborate with VPS service globally, working with other Teleflex sites, third parties and distributors to maintain a consistent approach to service | 3/15/2024 |
| 3087 | Zymo Research Irvine, CA Bioinformatics Associate I Holds a master’s or bachelor's degree in Biology, Bioinformatics, Computer Science, Mathematics, Statistics, or a related discipline. Experience may s Exp: 1+ years |
Zymo Research is seeking a highly motivated individual to join our Bioinformatics team! The qualified individual will play a key role in developing analysis pipelines for Next-Generation Sequencing data and performing cutting-edge data science to support Zymo Research’s global product strategy. As part of the Bioinformatics team, you will leverage your skills and familiarity with NGS-based sequencing methods in the research and development of new data analysis pipelines for our services, applications, and exciting research projects! | 3/15/2024 |
| 3088 | ZebraSci Mannford, OK; Tempe, AZ; Vernon Hil, OK R&D Engineer II B.S. degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering or other related engineering field. Mechanical Engineering degree Exp: 1-3 years |
Hybrid, Multiple Locations. This position is a limited term assignment which will include benefits such as (medical, health, dental, 401K). Eligibility for these benefits will be based on the eligibility requirements as determined by the BD Total Rewards policy and is anticipated to last approximately through 12/20/24. This position works multi-functionally and leads R&D activities needed in the development and transfer to manufacturing of products, processes, test methods and equipment for medical device manufacturing. Hybrid, Multiple Locations. This position is a limited term assignment which will include benefits such as (medical, health, dental, 401K). Eligibility for these benefits will be based on the eligibility requirements as determined by the BD Total Rewards policy and is anticipated to last approximately through 12/20/24. This position works multi-functionally and leads R&D activities needed in the development and transfer to manufacturing of products, processes, test methods and equipment for medical device manufacturing. | 3/15/2024 |
| 3089 | ZebraSci Lexington, MA Analytical Chemist Bachelor of Science degree required; Master of Science degree preferred. Exp: 1-year |
This position will be involved in many aspects of producing and developing biomaterials, including the analysis, production, isolation, purification and testing of biomaterials within well-defined guidelines. The associate will need to use appropriate analytical tools to characterize and qualify the biomaterials, such as gas chromatography (GC), gel permeation chromatography (GPC) and mechanical testing. S/he will interact with contract testing laboratories to conduct appropriate testing on the materials and may also provide supervision and guidance to junior level technicians. | 3/15/2024 |
| 3090 | ZebraSci Branchburg, NJ Combination Product Test Engineer Bachelors of Engineering, Biomedical, Chemistry, Biology, or equivalent is preferred. Exp: 1+ years |
Responsibilities Conducts timely sample intake, including receipt, proper identification, storage and return shipments as needed Conducts testing as assigned utilizing appropriate test methods, protocols specifications and equipment (includes product and/or equipment testing), including adhering to test schedules (e.g. stability pulls, aging pulls). Conducts data analysis as per protocol or specifications utilizing variety of data analysis tools (e.g. excel, JMP, MiniTab) Communicate challenges, scheduling or testing conflicts and other issues to management in timely manner Maintains inventory of lab supplies, including but not limited to; general supplies (e.g. PPE, wipes, cleaners…) and chemicals use for routine testing and/or cleaning Conducts routine sample disposition (e.g. return to client, disposal), including coordination of hazardous waste disposal Responsible to maintain the lab and storage areas in a clean an organized manner. Includes routine lab cleaning Adheres to ZebraSci Quality Systems, including but not limited to; timely identification, and notification of potential Quality Events (e.g. OOS, Deviations, CAPA…) and the subsequent forward processing and investigation of such events | 3/15/2024 |
| 3091 | ZebraSci Louisville, CO Staff Reliability Engineer BS in engineering or a related technical field (i.e., physics, materials science, mathematics). BS in engineering or a related technical field (i.e., Exp: 1-year |
The Staff Reliability Engineer is responsible for providing project support to ensure reliability targets are achieved according to project plans. The reliability engineer should have a demonstrated broad technical base in all aspects of reliability engineering. The ideal candidate would have experience in electrical, mechanical and software engineering fundamentals, including PoF (Physics of Failure) understanding. The candidate will work closely with R&D members and be a sole contributor to conduct system and component level reliability activities for sustaining product and new product development within the franchise and division. The reliability engineer will have the technical skills necessary to effectively challenge the design concepts as they pertain to overall reliability. An exciting part of the role includes opportunities to work on reliability initiatives for key R&D business critical projects. At the heart of reliability engineering is testing and we are looking for expertise that will help us become a Center of Excellence. The reliability engineer will lead troubleshooting and failure analysis investigation activities to determine design weaknesses and root-cause. Ideally the candidate will grow and be able to direct efforts of individuals around reliability process and deliverables | 3/15/2024 |
| 3092 | ZebraSci Temecula, CA Combination Product Test Engineer (Onsite) Bachelor’s degree in science or math related fields, such as biology, chemistry or engineering is preferred. Exp: 1 year |
The primary role of the Engineering Technician is the timely and accurate execution of testing as scoped within individual projects and per client requirements. This includes but is not limited to; sample receipt, prep, storage, and shipping, as well as protocol and report generation, data review and summary. This role utilizes standard and custom laboratory equipment. | 3/15/2024 |
| 3093 | ZebraSci Mebane, NC Associate Quality Scientist Bachelor’s degree in Biology, Microbiology or other related Life Science. Exp: 1-2 years |
Reporting to the Quality Scientist/Lab Supervisor, the BD Mebane Associate Quality Scientist is responsible for applying basic scientific principles to routine laboratory work, executing product testing, applying/interpreting scientific data of moderate complexity, ensuring good laboratory practices, and processing data generated from Quality Control testing. | 3/15/2024 |
| 3094 | ZebraSci Columbus, NB Quality Engineer I Bachelor's Degree Required Field(s) of Study: Science-related field, Quality Assurance, Engineering, Mathematics/Statistics Exp: 0-5 years |
Support Quality and Production groups by using process and regulatory knowledge combined with a data driven approach to problem solving. Become a subject matter expert in application of statistical tools, measurement systems analysis, and root cause analysis. Take ownership of projects and drive to completion, whether working independently or in a team. Will interact professionally with BDM, PS customers in project management and problem solving activities. Regular, punctual attendance is an essential job function. Ability to speak, read and write English. Ensures compliance with BD quality systems, policies, procedures and practices and all local, state, federal and BD safety regulations, policies and procedures. The applicant pool includes an identified internal candidate. All applications are welcomed | 3/15/2024 |
| 3095 | Accurus Biosciences Richmond, CA Research Associate Bachelor’s or Master’s degree in Biology. Exp: 0-3 years |
The successful candidate will perform a range of duty critical to our research service business. The primary responsibility of this position is general molecular biology which includes DNA cloning, site directed gene mutagenesis, plasmid DNA preparation and DNA restriction analysis. Additional responsibilities for this position may include mammalian cell culture, protein transient production, stable cell line generation and general lab maintenance. If interested, please send your resume to hr@accurusbio.com. | 3/15/2024 |
| 3096 | Affinivax Rockville, MD Biopharmaceutical Associate I Bachelor of Science / Bachelor of Art / Associates Degree in biological sciences, chemical sciences, engineering or equivalent technical discipline. Exp: 1+ years |
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Basic understanding and knowledge of the following areas and ability to perform the activity with some supervisory guidance: Follow appropriate standard operating procedures (SOPs), protocols and batch records/logbooks to safely perform process operations and document compliantly with good documentation and data integrity practices. Perform the set-up, operation, cleaning and break-down of process equipment. Perform sampling procedures on various analytical instruments to analyze cell culture, solution and/or product concentration characteristics. Operate Filter integrity devices to confirm the integrity of filters pre and post use. Perform process operations, equipment and instrument monitoring and trending to enable proactive identification of issues to escalate and correct with applicable departments. Follow all related safety policies and procedures and Put safety first by playing an active role in identifying and correcting unsafe behaviors and conditions. | 3/15/2024 |
| 3097 | Affinivax King of Prussia, PA Biopharm Manufacturing Associate II BS/BA degree OR an Associate’s degree from Montgomery county community college in Biotechnology or related technical field. Exp: 1+ years |
Posted Date: Mar 15 2024 Thank you for your interest in our Bio Pharm Manufacturing Associate II (Evergreen) position. Applicants for this role will not be receiving immediate feedback regarding their applications. If you are looking for an immediate opportunity, please take a look at the GSK careers page for opportunities that would align with your skill-set. I have included the link here for your convenience: Careers | GSK US . As a Biopharm Manufacturing Associate II, you will perform production operations including fermentation or cell culture operations, preparation of solutions, chromatographic separation, filtration and concentration operations, autoclave and parts washing of process assemblies, and area cleaning/upkeep. Will be responsible for completing daily manufacturing tasks, and increasing competency in different production areas over time. Will participate in safety and compliance initiatives, as well as investigations. Will engage in the GSK Production System to continuously improve safety, quality, and schedule/cost performance. | 3/15/2024 |
| 3098 | Affinivax King of Prussia, PA Associate Manufacturing Specialist Bachelors of Science, or Bachelors of Arts. Exp: 1+ years |
The Associate Manufacturing Specialist will be part of a high performing team responsible for delivering the supply of GSK products to the One Biopharm supply chain. They will demonstrate GSK Values (Patient Focus, Transparency, Respect, & Integrity) and Expectations (Courage, Accountability, Development, & Teamwork) on a daily basis by engaging positively with team members and production support groups. The associate manufacturing specialist, with support from team leads and supervisors, will perform a mix of tasks ranging from operation of GMP equipment, to leading pieces of work associated with supporting new product introduction and/or improvement of existing processes. The work this role will support will follow the lifecycle of new products, more specifically: Equipment/Facility Design, Technology Transfer, Commissioning & Qualification, Start-up & Engineering Batch manufacture, Process Performance Qualification batch manufacture, Clinical Supply, Commercial Supply, Changeover, Process Improvement. | 3/15/2024 |
| 3099 | Affinivax King of Prussia, PA Associate Microbiologist BS in science field. Exp: 1+ years |
GSK is currently looking for an Associate Microbiologist to join our team in Upper Merion, PA. In this role, the Microbiologist performs quality testing for In process and bulk biopharmaceutical ingredients, finished biopharmaceutical products. Reviews and revise SOP’s when needed. | 3/15/2024 |
| 3100 | Affinivax King of Prussia, PA Manufacturing Specialist Bachelors of Science, or Bachelors of Arts. Exp: 1+ years |
The Associate Manufacturing Specialist will be part of a high performing team responsible for delivering the supply of GSK products to the One Biopharm supply chain. They will demonstrate GSK Values (Patient Focus, Transparency, Respect, & Integrity) and Expectations (Courage, Accountability, Development, & Teamwork) on a daily basis by engaging positively with team members and production support groups. The associate manufacturing specialist, with support from team leads and supervisors, will perform a mix of tasks ranging from operation of GMP equipment, to leading pieces of work associated with supporting new product introduction and/or improvement of existing processes. The work this role will support will follow the lifecycle of new products, more specifically: Equipment/Facility Design, Technology Transfer, Commissioning & Qualification, Start-up & Engineering Batch manufacture, Process Performance Qualification batch manufacture, Clinical Supply, Commercial Supply, Changeover, Process Improvement. | 3/15/2024 |
| 3101 | Affinivax Hamilton, MT QC System Support Specialist Bachelor's Degree in a scientific discipline. Exp: 1+ years |
The QC Systems Support Specialist will manage non-testing laboratory support systems and processes for QC, including: Maintaining SAP Modules, Master Data/Monograph Creation, Compendial Review, Equipment Qualification/Lifecycle, and Method Validation/Transfer. Serve as a Lead Investigator for select QC Unplanned Events, as well as change coordinator for selected QC Change Controls. Author QC Technical Documents, such as validation and trend reports and provide data for annual PQR. Works collaboratively with global teams (ASAT) and the GSK network to maintain compliance and alignment, and to deliver both local and global projects as per established timelines. | 3/15/2024 |
| 3102 | Carmot Therapeutics Berkeley, CA Research Associate I/Research Associate II, Pharmacology BSc, MSc in pharmacology, biology or related field. Exp: 1-5 years |
In this position, you will assist with the design and execution of in vivo pharmacology experiments in rodents. In particular, you will be utilizing mouse models of obesity and diabetes to support compound characterization and mechanism of action studies. These efforts will support lead discovery and translational biology for clinical compounds. The position may also involve in ex vivo and in vitro pharmacology experiments. The environment at Carmot is fast paced, requiring you to be excellent at multitasking and working within a team to achieve common goals. | 3/15/2024 |
| 3103 | Cirtec Medical Sturtevant, WI Engineer I Manufacturing A bachelor’s degree in engineering. Exp: 0 years |
This position is primarily responsible for developing and implementing robust cost-effective manufacturing processes and methods in accordance with product specifications and Class III medical device quality standards. This position recommends and implements improvements to sustained production processes, methods and controls; as well as coordinates the launch of new products into pilot production. | 3/15/2024 |
| 3104 | Integrity Bio/ LyoTip Albuquerque, NM Mechanical Engineer Bachelor's degree (B.S.) in Mechanical Engineering. Exp: Entry level |
The Engineering Department provides the capacity to manufacture pharmaceuticals in an efficient, timely, and safe manner, thereby contributing to the profitability of the business unit by maintaining or modifying production equipment and related systems. The Mechanical Equipment Engineer will work in supporting manufacturing operations both on the manufacturing floor and off, spending time within the manufacturing operations is required and will be a priority at times. | 3/15/2024 |
| 3105 | Integrity Bio/ LyoTip Springfield, MO Process Engineer I or Process Engineer II The following required knowledge and proficiency skills are required for this position to be acquired through a minimum of a Chemical Engineering degr Exp: PE I: 0-3 years; PE II: 1-3 years. |
The primary purpose of the Process Engineer position is to design, implement and continuously improve chemical manufacturing processes using appropriate chemical engineering and scientific principles. Process design involves preparation of process flow diagrams, piping and instrument diagrams, mass and energy balances, equipment specifications, process safety information and operating procedures necessary to implement the process. Implementation involves development of construction task lists, participating in risk assessments, performing training, supporting start up and leading troubleshooting efforts. Continuous improvement includes identification of opportunities to improve quality, safety and economic performance of processes through proactive engineering evaluation as well as incident investigation and corrective/preventative action identification and implementation. Secondary purposes include configuration, modification and optimization of site control systems and to provide technical assistance to other site departments (QA, QC, Accounting, Maintenance, EH&S, etc.) in support of Curia's general business objectives and requirements. | 3/15/2024 |
| 3106 | Integrity Bio/ LyoTip Albany, NY Research Scientist I; Analytical Development Bachelor’s or Master’s Degree in Chemistry or a related field. Chemical Hygiene training. Exp: 1+ years |
The Research Scientist I-Analytical Development is an integral part of the Curia team, contributing to our success by supporting the manufacturing department and external customers. The routine functions of the laboratory are testing of raw materials, in-process, end product, and stability samples. The principal responsibility of the Research Scientist I is the analysis by multiple procedures of compounds. The Research Scientist I is expected to demonstrate proficiency in both the theoretical and practical aspects of analytical chemistry. | 3/15/2024 |
| 3107 | Integrity Bio/ LyoTip Albany, NY Research Scientist I; Analytical Development Bachelors or Masters Degree with major in Natural Science or Pharmacy or equivalent. Chemical Hygiene training. Exp: 1+ years |
The principal responsibility of the Research Scientist I is the analysis by multiple procedures of intermediates and target compounds. The Research Scientist I is expected to demonstrate expertise in both the theoretical and practical aspects of analytical chemistry. A major component in the scientist's performance rating will be based on productivity. | 3/15/2024 |
| 3108 | Integrity Bio/ LyoTip Rensselaer, NY Production Technician in Rensselaer, NY - 12 Hour Nights Associates or Bachelor's degree. Exp: 1+ years |
The Production Technician is an integral part of the team, contributing to our success by weighing out chemicals and preparing various types of solutions for use in process. | 3/15/2024 |
| 3109 | Integrity Bio/ LyoTip Burlington, MA Quality Assurance Specialist I, Sun-Wed 7a-5p Bachelor’s degree (or foreign equivalent) in Biology, microbiology, biotechnology or related life science field. Exp: 0-3 years’ |
The Quality Assurance Specialist I is responsible for maintaining Quality databases and providing on-the-floor QA presence and oversight to the manufacturing operation. The QA Specialist’s role will include identifying compliance risks in the operation prior to and during execution, avoiding deviation whenever possible as well as managing immediate corrective action such that a) adherence to cGMP’s and internal procedures/policies is maintained, b) appropriate immediate corrective action is implemented and effectively documented in order to provide traceability and substantiation of any claims to be made in the investigation. This position primarily works in the cGMP production areas to manage adherence to the quality system and to initiate and assist in the initiation and resolution of deviations. | 3/15/2024 |
| 3110 | Integrity Bio/ LyoTip Albuquerque, NM Aseptic Core Monitor I BS, preferably in Microbiology or a related field. Exp: 1+ years |
Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The Aseptic Core Monitor (Albuquerque, NM) will oversee all activities in the aseptic environment to ensure continual compliance with cGMP and provide mentoring on aseptic techniques for all aseptic personnel. This position requires expertise in all aspects of aseptic manufacturing of the sterile product, the ability to work hands-on, strong leadership skills, and the ability to collaborate in a cross-functional environment. The individual will work closely with all departments in the manufacturing environment and reports metrics to site management regularly. Join our talented workforce, where a commitment to excellence and a customer-focused attitude is everything. We pursue excellence because our work has the power to improve patient’s lives with the pharmaceuticals we develop and manufacture. | 3/15/2024 |
| 3111 | Roche Seattle, WA Research Associate Bachelor’s, Master’s or PhD degree in Biological/Life Sciences, Chemistry, Organic Chemistry, Chemical Engineering, Biochemistry or related field. Exp: 1+ years |
Roche Diagnostics acquired Stratos Genomics (SBX Nanopore Sequencing) in 2020 for its unique chemistry that advances DNA sequencing by nanopore, Sequencing by eXpansion (SBX™). You will develop, process and purify the molecular building blocks for our novel technology. These building blocks translate DNA sequences into a simple to measure surrogate, the Xpandomer, which significantly improves the accuracy and throughput of nanopore sequencing. The Molecular Engineering group is passionate about the novel molecules they have developed and the impact SBX technology can have on advancing sequencing and patient outcomes. We are looking for people who are excited to collaborate with us to make SBX successful. Please include a cover letter outlining why you want to work with us, your specific interest in our technology and how you would contribute. | 3/5/2024 |
| 3112 | Roche Branchburg, NJ Senior Lab Technician Associates degree required; Bachelor's Degree preferred. Exp: < 1 year |
Branchburg is the molecular diagnostics manufacturing engine within Global Operations and a Polymerase Chain Reaction (PCR) center of excellence. As the largest DIA manufacturing site in North America, our teams deliver a broad portfolio of PCR-based in-vitro diagnostic tests. Our operations include reagent and active diagnostic ingredient (ADI) production, filling and packaging. Our 63-acre site with ~1400 people is currently under expansion, fueled by our culture of agility, innovation and transformation. Each day we focus on delivering the value of Roche Diagnostics to patients around the world. | 3/5/2024 |
| 3113 | Roche Carlsbad, CA Mechanical Engineer I BS degree. Exp: 0-2 years |
We are looking for a highly motivated and team-oriented individual who is passionate about technology and product development for IVD assays. As a Mechanical Engineer I, you will work under supervision from senior contributors for concept-to-market and sustaining engineering efforts of IVD instrumentation. Apply hands-on involvement in on-market support for existing and new products, troubleshooting and root cause analysis, creation and maintenance of input and output specifications, concept and feasibility activities, prototyping, testing, and transfer to manufacturing. | 3/5/2024 |
| 3114 | Roche Santa Clara, CA Product Engineer B.S. in Biology, Chemistry, Biochemistry, Molecular Biology, Mechanical Engineering or a related field. Exp: 1-3 years |
As a Product Engineer at Roche Sequencing Solutions, you will be instrumental in the development of the consumable prototype manufacturing process. In this dynamic role, you will lead the charge in innovation, contributing to the advancement of highly automated DNA sequencing pipelines and diagnostic applications. Your expertise will play a critical role in shaping the future landscape of genetic diagnostics. Roche is seeking a motivated and collaborative individual with strong analytical skills to join our team. As a Product Engineer, you will drive the development of high-quality devices, serving as a key player in the development and technology transfer of our prototype manufacturing process. This position entails close collaboration with internal and external hardware and software developers within the RSS team, as well as active engagement with the CD development team. | 3/5/2024 |
| 3115 | Roche Carlsbad, CA Process Engineer I - Night Shift Bachelor’s degree in Engineering or a related technical discipline. Exp: 1+ years |
The work schedule for this position is a night shift from Sunday through Friday from 10 PM to 6:30 AM. As a Process Engineer you are responsible for driving stable, reliable production processes. You are instrumental in troubleshooting, testing , and supporting for existing products and new product lines. Under minimal supervision, you will apply engineering principles to resolve complex manufacturing equipment issues that arise and implement initiatives to reduce equipment downtime and improve throughput yields. | 3/5/2024 |
| 3116 | Roche Carlsbad, CA Quality Control Specialist I - Mon-Fri 4:30 PM to 1 AM B.S. degree required, in basic sciences, life sciences, or engineering. Exp: 1 - 3 years |
This position conducts incoming, in-process and final release QC testing in a controlled manufacturing environment. This position may also execute validation studies, execute test protocols, analyze data, generate analytical reports, investigate Non-Conformances, evaluate processes & procedures, utilize statistical techniques, review specifications, and inspect & test equipment. May conduct training on quality related tools, methods, and procedures. Interfaces with R&D, Manufacturing, Quality, and Supply Chain within the company and when appropriate with customers and suppliers on quality related issues. | 3/5/2024 |
| 3117 | Roche Tucson, AZ IQC Technician II Bachelor's Degree preferred. Exp: < 1 year |
The Incoming Quality Control (IQC) Technician – Instruments Manufacturing, will be an integral part of a team that performs inspection of raw materials, components and sub-assemblies using established operation procedures, work instructions, engineering parts drawings. The individual will be responsible for the review, generation and sign-off of inspection reports and related quality documentation. The individual will be responsible for interfacing with highly complex systems and controls in an ISO 13485 and GMP manufacturing environment. The individual will maintain areas in high state of inspection preparedness by maintaining equipment, records and IQC environment in order to comply with regulatory requirements utilizing current regulations and Operating Procedures (OP). Additionally, maintains incoming inspection documents, assists in the investigation of incoming parts and instruments manufacturing non-conforming parts, manufacturing exception events and works independently with general guidance from senior team members. | 3/5/2024 |
| 3118 | RPRD Diagnostics Wauwatosa, WI Clinical Lab Technician I Bachelor's degree in genetics, biology, molecular biology, chemistry, biochemistry or related discipline. Exp: 1 year |
RPRD Diagnostics, LLC is seeking a Clinical Lab Technician I to join our team. At RPRD, we believe that comprehensive genetic testing offers an unprecedented opportunity to improve the outcomes for millions of patients who are prescribed drugs, so we are developing next-generation pharmacogenetics testing services to improve clinical decision making. We aim to enable hospitals, clinicians, and their patients to better understand and manage their treatment choices on the basis of each individual's unique genetic profile. Additionally, our team is committed to continuous innovation in order to advance knowledge and deliver cutting edge services and care to our clients and their patients. The Clinical Lab Technician I performs high complexity molecular techniques such as genotyping, next generation sequencing, data analysis and interpretation. They are further responsible for recognizing the clinical significance of each test performed, maintaining the confidential and sensitive nature of patient information and results, and reporting results within established time frames. This position also assists with the validation of new applications in the clinical laboratory and works collaboratively as part of a team to help ensure the smooth operation of the lab. | 3/5/2024 |
| 3119 | SAMDI Tech Worcester, MA Research Technician I Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months |
We have an exciting opportunity for a Research Technician I (Sunday through Thursday hours) at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. | 3/5/2024 |
| 3120 | SAMDI Tech Worcester, MA Research Technician I - 2nd Shift Hours Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months |
We have an exciting opportunity for a Research Technician I (Monday through Friday 2nd shift hours) at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. | 3/5/2024 |
| 3121 | SAMDI Tech Mattawan, MI Technician 1 - Histology, 2nd Shift Bachelor’s degree (BA/BS) or equivalent in a biological science, preferred. Exp: 0+ months |
We are seeking an experienced Technician 1 - Histology for our 2nd Shift Pathology Services Team in Mattawan MI. A Technician 1 – Histology is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to conduct a study, which may include handling tissues and organs, trimming tissues, embedding, measuring organ weights; microtomy, slide preparation, staining; inventory and quality control, and shipping of tissues. The technician is working under close supervision to gain proficiency. | 3/5/2024 |
| 3122 | SAMDI Tech Cambridge, MA Research Associate /Imaging Bachelor’s degree (B.A./B.S.) or equivalent in Animal Science or related field. Exp: One to two years |
We are seeking an Research Associate/ Imaging for our Insourcing Solutions Department based in Cambridge, MA. As the Research Associate/Imaging, you will perform multi-modality imaging studies, preclinical imaging data acquisition, image data processing and analysis, may also work with other scientists for in vivo and ex vivo imaging experiments. | 3/5/2024 |
| 3123 | SAMDI Tech Horsham, PA Formulations Technician I Bachelor’ degree (B.S.) preferred. Exp: 0 to 1 years |
Full Time – 40 Hours/Week $1000 SIGN ON BONUS (external applicants eligible only) Perform routine preparation of vehicles and test article dosage solutions for use in toxicology studies with close supervision. | 3/5/2024 |
| 3124 | SAMDI Tech Wayne, PA Technician I Molecular Biology Bachelor's degree (B.A./B.S.) or equivalent in Biology or related discipline. Exp: 0-1 years |
Under direct supervision, responsible for performing daily laboratory tasks as they relate to Molecular Biology Testing Services. | 3/5/2024 |
| 3125 | SAMDI Tech Malvern, PA Technician I Microbiology Bachelor's degree (B.A./B.S.) or equivalent in Biology or related discipline. Exp: 0-1 years |
Under direct supervision, responsible for performing daily laboratory tasks as they relate to Molecular Biology Testing Services. | 3/5/2024 |
| 3126 | Sanofi Pasteur Framingham, MA Purification Development Research Associate Bachelor's degree in Chemical Engineering, Biochemical Engineering, Biochemistry or related discipline Exp: 1+ years |
We are looking for candidates for the position of Research Associate. This individual will join a dynamic and motivated team to develop downstream purification processes in support of early and late stage drug development programs. In addition, the Research Associate will support the tech transfer of the developed process into the clinical manufacturing team or Industrial Affairs organization, while ensuring the highest standards of safety, environmental, and regulatory compliance are maintained in the workplace. | 3/5/2024 |
| 3127 | Sanofi Pasteur Swiftwater, PA Production Technician - Vaccine Associates or Bachelor’s Exp: AS: 1 + yrs; BS: 0 + yrs |
This is a third shift position. Must be able to work weekends and holidays as needed. Flexibility for changing schedule required. | 3/5/2024 |
| 3128 | ScienCell Research Laboratories Carlsbad, CA Associate Molecular Biologist Bachelor’s or Master’s degree in life science. Exp: one-year |
We are searching for an energetic and self-motivated candidate with a positive attitude and strong work ethic to fill our associate molecular biologist position in our R&D department. Responsibilities include, but are not limited to, working on cell-derived DNA, RNA, and proteins purification, gene expression analysis, performing PCR/RT-PCT/qPCR, SDS PAGE and UV spectrum for quantitation. Candidates should be familiar with electrophoresis, spectrophotometer, centrifugation and other basic laboratory techniques. General lab logistical skills such as record keeping, ordering supplies and ensuring general laboratory safety and cleanliness are also required. | 3/5/2024 |
| 3129 | SeaGen Groton, CT Associate Scientist, Sustainable Chemistry Data Bachelor’s Degree in Chemistry, Environmental Science or related field. Exp: 0 to 2 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will become a member of Pfizer Chemical Research and Development (CRD) Sustainability Team, and will work under the guidance of the Sustainable Chemistry Lead. Your work alongside the entire department will help implement an overall strategy for the collection, analysis, management, and communication of sustainability related data and metrics. You will help execute the CRD Vision by measuring key sustainable metrics evolution over time as we commit to the development of greener processes to manufacture Pfizer APIs from clinical to commercial. Your role will support the company towards its goal of becoming Net Zero by 2040. You are able to work independently or within a small team under guidance from strategy leaders.Essential skills include excellent oral and written communication, proficient office computer software knowledge including data management (Microsoft Office, Spotfire) and teamwork-oriented mindset. Ideally, you have a solid knowledge of organic chemistry and you are passionate about data collection as well as sustainability. | 3/5/2024 |
| 3130 | SeaGen Bothell, WA Manufacturing QA Associate III Bachelors Degree Exp: 0+years |
You will be a member of Pfizer’s dedicated and highly effective quality assurance team. You will evaluate and review Pfizer’s clinical and commercial batches of drugs. You will make sure that product and process documents match the specifications based on established sampling and statistical process control procedures. Your expertise will help in identifying deviations from established standards, in the manufacturing of products. In the relevant cases you will approve investigations and change control activities to ensure compliance with configuration management policies. As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues. It is your hard work and commitment that will make Pfizer ready to achieve new milestones and help patients across the globe. | 3/5/2024 |
| 3131 | SeaGen Rocky Mount, NC Associate Validation Engineer Bachelors degree Exp: 0+years |
You will be a member of Pfizer’s dedicated and highly effective Validation team. You will be responsible for the creation, review and approval of validation master plan, SOPs, protocols and reports. Your methodological approach will help us ensure compliance of our quality systems with company standards and government regulatory requirements. Your problem-solving ability will help us troubleshoot validation problems for equipment and performance processes and conduct statistical analysis of testing results and process anomalies. Your documentation skills will guide the writing, review and approval of validation process documents and technical reports related to equipment, facilities, utilities, computer systems, products and processes. As an Associate Validation Engineer you will be responsible for validating/qualifying the systems, equipment, utilities used to manufacture and/or clean drug products within a large manufacturing facility located in North Carolina, USA. You will help to demonstrate systems are running according to necessary specifications and operate within regulations to ensure data integrity and the production of quality products. | 3/5/2024 |
| 3132 | SeaGen Kalamazoo, MI QC Laboratory Analyst II Bachelor’s degree in Chemistry, Biochemistry or related science. Exp: 0-1 years |
This position is for a testing analyst in the Kalamazoo QO API Non-LC Laboratory working on first shift. Opportunity for schedule flexibility exists as the Laboratory supports business and customer needs on weekends and holidays. Technologies employed in the API NonLC Laboratory include GC, Particle Size, X-Ray Crystallography, Karl Fisher, UV, and general analytical procedures. | 3/5/2024 |
| 3133 | Seracare Life Sciences Cumberland Foreside, ME Quality Control Technologist I Associates in Medical Laboratory Science or a Bachelor’s degree in Medical Technology (preferred) or related science degree (i.e. biology, chemistry, Exp: 1-3 years |
Follows standardized procedures and prepares samples for testing. Analyzes test results for accuracy, acceptability, and critical limits. Relies on limited independent judgment to plan and accomplish goals. Performs a variety of tasks. A limited degree of creativity and latitude is required. | 3/5/2024 |
| 3134 | Shionogi San Diego, CA Laboratory Assistant, Qpex BioPharma, wholly-owned subsidiary of Shionogi Inc. in San Diego, CA. Associates degree or a relevant certificate in a laboratory science field. Exp: 1+ years |
As a Lab Assistant you will play a vital role in supporting scientific and research activities within Qpex’s research laboratory. | 3/6/2024 |
| 3135 | Sigmapharm Laboratories Bensalem, PA Quality Assurance Associate At minimum, an associate’s degree in any life science. Exp: 1 to 3 years |
· Responsible for assisting the Head of Quality Assurance (QA) to ensure all pharmaceutical processes and documentation that may impact the safety, identity, strength, quality and purity of any drug product or drug substance manufactured at Sigmapharm Laboratories, LLC (Sigmapharm) complies with all applicable Standard Operating Procedures (SOPs) and regulatory requirements and is prepared or performed in a way that maintains quality and reduces potential risks. · Responsible for the review and approval of all product and process-related Official Documents. · Responsible for the review and approval of qualification related Documents such as protocols and reports. · Responsible for aiding in the control and organization of CGMP documentation, recorded information or data generated and maintained in document control. · Responsible for auditing batch records and overall operational procedures. | 3/6/2024 |
| 3136 | Smithers West Trenton, NJ Scientist (PCR and Molecular Biology) MS in Biological or Physical Sciences. Exp: 1-2 years |
Smithers PDS LLC (Pharmaceutical Development Services) assists in the development of new medicines by providing bioanalytical services for all phases of drug development from discovery through approval and post market surveillance. PDS works with customers to develop new methods, validate existing methods, and perform the assays necessary to analyze samples from patients on more than 100 clinical trials. PDS is seeking a Scientist with experience in Molecular Biology to join our team. The successful candidate is able to apply prior experience and knowledge to successfully perform in a laboratory environment under regulated conditions. | 3/6/2024 |
| 3137 | Smithers Darien, IL Associate Chemist I - Smithers Cannabis Testing Services, Darien, IL BS degree in Chemistry or related field. Exp: 6 months |
Smithers Cannabis Testing Services is seeking an Associate Chemist I at our Darien, IL location. Job Summary The Associate Chemist I performs critical sample processing and extraction duties to prepare cannabis samples for analysis and enters sample information in the laboratory information management system (LIMS) to facilitate subsequent analysis. The position is responsible for maintenance of laboratory stock reagents. Operates and may maintain, under supervision, test equipment and apparatus. | 3/6/2024 |
| 3138 | Smithers Wareham, MA Assistant Biologist - Ecotoxicology - Smithers Wareham, MA Bachelors or better in Biology or related field. Exp: 0+ years |
Smithers Environmental Risk Sciences division is seeking an Assistant Biologist in the Ecotoxicology Department at our Wareham, MA location. Often, duties include recording instrument and apparatus readings, making observations of various biological effects in exposures and compiling study data books. Incumbent will be introduced to mathematical and statistical procedures used to reduce and analyze study data. Responsible for maintaining cleanliness of the labs, storage and culture areas including maintenance and calibration of equipment used in any of these settings. May require routine involvement in seawater and/or sediment collection. Assignments are completed with minimal supervision. Assists with organization, direction and training of technicians. Assists in coordinating internal requirements for testing (i.e. chemistry support, Quality Assurance, reporting). Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations and company policies. | 3/6/2024 |
| 3139 | Smithers Wareham, MA Associate Chemist I - Environmental Fate and Metabolism B.S. degree in chemistry or related field. Exp: 6 months |
Position is expected to perform a variety of routine tasks and often complex and difficult procedures independently and under supervision, in support of the conduct of normal laboratory operations. Individual is expected to detect and report problems in standardized procedures due to instrumental, sample, or test system failures. Performs a variety of routine, laboratory-based procedures. Responsible for understanding and routinely performing applicable Standard Operating Procedures, study specific protocol procedures and other laboratory assignments. This often includes recording instrument and apparatus readings on standard forms, preparation of test systems and recording and compiling laboratory data in real time in a complete and thorough manner for individual assignments. Responsible for maintaining cleanliness of the labs, storage and chamber areas as well as executing regular maintenance/calibration of equipment used on a regular basis. Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations as well as company policies. Duties are performed with minimal supervision. | 3/6/2024 |
| 3140 | Smith and Nephew Pittsburgh or Andover, PA Software Engineer (Pittsburgh, PA or Andover, MA) Bachelor’s degree required (Software Engineering or Computer Science preferred). Exp: 0 - 2 years |
Software Engineer (Pittsburgh, PA or Andover, MA) Life Unlimited. At Smith+Nephew, we design and manufacture technology that takes the limits off living. The Software Engineer will be involved in research/design/testing of medical devices | 3/6/2024 |
| 3141 | Spherotech Lake Forest, IL Manufacturing Associate Bachelor's degree in Chemistry or related field. Exp: 0+ years |
Spherotech, Inc. seeks a college graduate for a Manufacturing Associate opening. Duties include polymer synthesis, bottling, packaging, documentation, etc. | 3/6/2024 |
| 3142 | Spherotech Lake Forest, IL Quality Control Associate Bachelor's degree in Chemistry or related field. Exp: 1 year |
Spherotech, Inc. seeks a college graduate for a Quality Control Associate opening. Duties include final product inspection, documentation, Quality Control testing etc. | 3/6/2024 |
| 3143 | Stability Biologics San Antonio, TX QA Specialist - San Antonio, TX BS degree in a scientific discipline (Chemistry, Biology, Physics, Bio-Medical Engineering/Chemical Engineering, etc.). Exp: 1 year |
The Quality Assurance Specialist (QAS) will be a member of the Stability Biologics Quality Dept. to perform quality record reviews, batch release, record retention, data entry, auditing, investigations and document control activities. The QAS will be responsible for quality assurance metrics, CAPA/NCMR and maintaining all quality records/batch records in a secure and controlled manner. The QA Specialist will also be responsible for ensuring all policies and procedures are in compliance with appropriate FDA, AATB, states, and Stability Biologics standard operating procedure. | 3/7/2024 |
| 3144 | StageBio Frederick, MD Laboratory Technician I/II/III · College degree preferred. Exp: 0+ years |
StageBio is seeking a full-time Laboratory Technician II to join our Frederick, Maryland facility. Primary Responsibilities Include: Individuals will be trained to perform tissue grossing, processing, embedding, microtomy, staining (H&E & special staining), quality control and general histology duties Maintain a safe working environment by following all safety and chemical regulations as outlined in StageBio’s SOPs Prompt and accurate recording of data Daily cleaning of work area and equipment Other duties assigned by management | 3/7/2024 |
| 3145 | Stellartech Research Milpitas, CA Quality Engineer II Typically requires a BS degree or equivalent. Exp: 1-3 years |
Stellartech is looking for a Quality Engineer to join our Team. | 3/7/2024 |
| 3146 | Tempus Durham, NC Molecular Technologist - Lead Trainer (Monday-Friday, 2:30pm-11:00pm) MS in medical technology, clinical laboratory science, chemical, physical or biological science. Exp: 1 year |
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time. With the advent of genomic sequencing, we can finally decode and process our genetic makeup. We now have more data than ever before but providers don't have the infrastructure or expertise to make sense of said data. Here at Tempus, we believe the greatest promise for the detection and treatment of cancer lies in the deep understanding of molecular activity for disease initiation, progression, and efficacious treatment based on the discovery of unique biomarkers. We're on a mission to connect an entire ecosystem to redefine how genomic data is used in clinical settings. We're looking to build a laboratory team who are passionate and focused on developing state of the art techniques to processing and creating and interpreting vast amounts of genomic and molecular data. | 3/8/2024 |
| 3147 | Tempus Durham, NC Molecular Technologist - Lead Trainer (Monday-Friday, 8:00am-4:30pm) MS in medical technology, clinical laboratory science, chemical, physical or biological science. Exp: 1 year |
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time. With the advent of genomic sequencing, we can finally decode and process our genetic makeup. We now have more data than ever before but providers don't have the infrastructure or expertise to make sense of said data. Here at Tempus, we believe the greatest promise for the detection and treatment of cancer lies in the deep understanding of molecular activity for disease initiation, progression, and efficacious treatment based on the discovery of unique biomarkers. We're on a mission to connect an entire ecosystem to redefine how genomic data is used in clinical settings. We're looking to build a laboratory team who are passionate and focused on developing state of the art techniques to processing and creating and interpreting vast amounts of genomic and molecular data. | 3/8/2024 |
| 3148 | NeoLight Scottsdale, AZ Biomedical Engineer Bachelor's Degree in Electrical Engineering (Required) from an accredited university or college. A Master's degree is preferred. Exp: entry-level or 1-2 years |
We seek a full-time entry-level Biomedical Engineer focusing on Electrical Engineering. In this role, you will provide strong, independent technical support to teams that contribute to resolving significant electrical and embedded system issues for the next generation and on-market products. A successful candidate will be a productive individual contributor who works independently with general supervision on larger, moderately complex projects/assignments. In addition, the candidate sets objectives for their job area to meet the objectives of projects and assignments. | 3/8/2024 |
| 3149 | TransMedics Andover, MA Mechanical Engineer I - Product Development BS in Mechanical Engineering, Plastics Engineering, Biomedical Engineering, or equivalent is required. Exp: 0-2 years |
Reporting to the Director of Mechanical Engineering, the Mechanical Engineer 1 will work with the cross- functional Product Development team to develop new products. The ideal candidate should be self- motivated and have a strong desire to learn and take on new responsibilities. The candidate will support larger programs under the mentorship of Sr. Staff and lead smaller projects with guidanace. The candidate will contribute to the full design process from concept to production. This position will have several opportunities to develop engineering skills including: CAD, technical analysis, technical writing, problem solving, engineering best practicices, and hand-on use of lab and machine shop equipment. | 3/8/2024 |
| 3150 | TransMedics Andover, MA Cardiothoracic Research Specialist Bachelor's degree in Biology, Biochemistry, Biomedical Sciences or related field. Exp: 1–2-year |
If you’re looking for a career with a company where you can make a difference, earn a competitive salary, and have ample professional growth opportunities, this is it. TransMedics is a publicly traded, medical technology company revolutionizing what’s possible in organ transplant through innovation, collaboration, and commitment. We’re growing and transforming the transplantation industry through our Organ Care System (OCS™) technology platform & National OCS Program, preserving organs used in heart, lung, and liver patienttransplants for safe transport nationwide. We are seeking a highly motivated and detail-oriented Cardiothoracic Research Specialist to joinour Cardiothoracic Research team. This position offers an excellent opportunity for an early career researcher to gain hands-on experience in cardiothoracic research while contributing tomeaningful projects within our dynamic research and lab environment. | 3/8/2024 |
| 3151 | Pharmaron San Diego, CA In Vivo Research Associate I, Ophthalmology Associates degree (preferred) in veterinary technology or BS. Exp: AS: 1-2 years; BS: 1 year |
Pharmaron (San Diego) is seeking to hire an outstanding candidate to join our Ocular department at the Research Associate I level. The Research Associate will play an important role by supporting in vivo studies to test devices being developed for various ocular disorders. | 2/27/2024 |
| 3152 | Pharmaceutics International Hunt Valley, MD Microbiologist (EM) B.S / M.S. in a life sciences discipline. Exp: 0-2 years |
Executes the activities of QC Microbiology Laboratory by following approved microbiological and chemical test procedures and ensuring their delivery in an accurate and timely manner following proper safety precautions. | 2/27/2024 |
| 3153 | Phitonex Fremont, CA Scientist I, Formulations BS/BA in scientific field in Chemistry, Biochemistry, ore related technical discipline. Exp: 1+ years |
You will be responsible for manufacturing products for the Bulk Formulations Toxicology team and complete associated cGMP documentation. You will work with chemicals and biologicals to manufacture reagents, calibrators, and controls for IVD immunoassay use and participate in process improvements projects. | 2/27/2024 |
| 3154 | Phitonex Florence, SC Scientist I - Process R&D BS/BA degree in chemistry or life science. Exp: 0-3 years |
You will join a team of synthetic organic chemists in the manufacturing of pharmaceutical ingredients at the Florence, SC site. Many of our products are already in the market serving patients and we work on a variety of projects for existing and new clients. In this position, you will perform hands-on experimentation and learn knowledge and skills for the process development of pharmaceutical products. We have a fast-paced working environment while keeping a good work-and-life balance. | 2/27/2024 |
| 3155 | Phitonex Cincinnati, OH R&D/Mfg Scientist I (onsite) Associates or Bachelor’s Degree in physical science; Chemistry or Biology preferred. Exp: 1-2 years |
As a Quality Laboratory Team Member, you will coordinate with your supervisor and collaborate with colleagues in diverse groups to assure that critical timelines are met. You will have the opportunity to collaborate with your peers within the laboratory and those in other departments such as formulations, operations, project management and quality assurance on a regular basis. You will perform analytical methods for elaborate testing for validated and experimental methods and other tests as needed to support lab operations. You will participate in the validation of analytical test methods when additional resources are required. | 2/27/2024 |
| 3156 | Phitonex Middletown, VA Formulation Scientist I B.S. in Science or Medical Technology is preferred. Exp: 0+ years |
Work in a Value Stream environment and organize, carry out, monitor, multi-stage production processes to prepare and formulate serum, clinical diagnostic assays and reagents for use in research and commercial scientific products for the IVD industry with compliance to specifications and GMP/FDA requirements. The formulations range in scale from 1 mL to 50,000 L and are manufactured using protocols/batch records in an environmentally monitored lab space. Data is recorded in batch records following good documentation practices as required for regulated industries. | 2/27/2024 |
| 3157 | Plex Pharma San Diego, CA Research Associate, Biology & Protein Chemistry BS or MS in molecular and biology, protein chemistry or related field. Exp: 1-3 years |
Plex Pharmaceuticals (www.plexpharma.com), a biotechnology company with a focus on developing novel drugs targeting misfolded and aggregated proteins, has an immediate opening for a Research Associate. The successful candidate will contribute to drug discovery efforts by performing cloning, expression and purification of protein drug targets, as well as assisting in assay development and characterization of compounds. | 2/27/2024 |
| 3158 | Poochon Proteomics Solutions Frederick, MD Lab Assistant Associate degree or above in medical technology, or related life science is preferred. Exp: 1+ year |
We are seeking a Lab Technician to join our DNA Sequencing and Mass Spectrometry team. | 3/1/2024 |
| 3159 | PPD Middleton, WI Entry Level Biochemist Bachelor's degree or equivalent. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 3/1/2024 |
| 3160 | PPD Highland Heights, KY Assistant Scientist - 2nd Shift Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 3/1/2024 |
| 3161 | PPD Highland Heights, KY Assistant Scientist Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 3/1/2024 |
| 3162 | Prevail Therapeutics Boston, MA Associate Scientist, Early Preclinical Development - Inner Ear Biology Bachelor's Degree. Exp: 0+ years |
The Early Preclinical Development (EPD) Team is seeking an Associate Scientist with experience in inner ear histology to support discovery and IND-enabling animal studies. The ideal candidate will have experience in histologic techniques specific to the inner ear, such as microdissection of the mouse and non-human primate (NHP) inner ear tissues into discrete anatomical regions, and further processing of these tissues using various histologic techniques, in addition to imaging, analysis, and preparation of data for presentation. Cross-functional work may be required to advance Company goals. The successful candidate will be self-motivated and creative, with a desire to succeed at the highest level in a highly collaborative and fast-paced environment. | 3/1/2024 |
| 3163 | Prevail Therapeutics San Francisco, CA Research Associate - DMPK DICE BS or MS in chemistry. Exp: 0-6 years |
We seek an exceptional full-time lab-based Research Associate to join our Drug Metabolism and Pharmacokinetics (DMPK) team. This individual will be a key contributor to performing standard ADME/DMPK assays, such as microsomal stability, plasma protein binding, and metabolite identification. The individual will also be responsible for operating LC-MS instruments (QQQ and HRMS) with minimal direction. Do you have experience in mass spectrometry while doing enzyme related work? This role may be perfect for you! | 3/1/2024 |
| 3164 | Preventice Solutions Arden Hills, MN Quality Engineer I - Electrical Bachelor's degree or higher in Electrical Engineering. Exp: Entry-Level |
The Electrophysiology (EP) Design Quality Assurance team is looking for an engineer to evaluate manufacturing and design changes. EP has a broad portfolio of capital equipment used in the field to support ablation and diagnostic procedures. The EP Design Quality assurance team is growing, and the timely evaluation of design changes is key to maintaining a robust EP Capital Equipment portfolio to reduce potential safety and quality issues. This role provides visibility across the Research and Design organization. The selected candidate will collaborate with Manufacturing, Product Complaints, Regulatory, and Field Servicing engineering. This is a significant role for an entry-level engineer with opportunities to grow into Computer Programming, Cybersecurity, Risk, or Electrical Design. The selected candidate will be mentored by a Senior Electrical Engineer. | 3/1/2024 |
| 3165 | Preventice Solutions Maple Grove, MN Quality Engineer I University degree or the equivalent combination of education and experience required. Exp: 0-2 years |
Develops, establishes and maintains quality engineering methodologies, systems, and practices which meet BSC, customer, and regulatory requirements. Serves as a Quality representative to improve awareness, visibility, communication on quality initiatives to support departmental, functional, site, divisional and corporate quality goals and priorities. Provides focused quality engineering support within new product development, operational, or system/services support. | 3/1/2024 |
| 3166 | Procept BioRobotics San Jose, CA Electrical Engineer Bachelor's degree (B.S.) in Electrical Engineering or equivalent. Advanced degrees are a plus. Exp: 1-5 years |
The Electrical Engineer works within the Electrical Engineering group within the R&D Capital Equipment department. The position will be responsible for supporting electrical systems for PROCEPT’s electro-mechanical products, including electronics feasibility, requirements definition, design, design verification, test system development, manufacturing procedure development, and production transfer activities at various stages of the product development cycle. Development will be conducted in accordance with PROCEPT’s quality system. | 3/1/2024 |
| 3167 | ProteinSimple Minneapolis, MN Advanced Research Associate MS degree in the biological sciences. Exp: 0-2 years |
As an Advanced Research Associate you will work in the Immunocytochemistry Department on the validation of antibodies for immunocytochemistry applications. You will be knowledgeable of animal anatomy and histology and familiar with histological examination of tissues, frozen and paraffin-embedded tissue sections, immunohistochemistry protocols, microscopy systems; collect digital images, digital image post-processing and enter data into a database. | 3/1/2024 |
| 3168 | ProteinSimple Newark, CA Senior Research Associate, PAS MS in molecular biology, biochemistry, cell biology or related field. Exp: 0-2 years |
The Senior Research Associate (SRA) will serve as a key member of the ACD Professional Assay Services (PAS) department, performing RNAscope assay services for industrial, pharmaceutical, and academic sponsors to detect RNA targets of interest. An additional critical work component will be the application of immunohistochemistry (IHC) to look for specific protein targets. The position will have an opportunity to work closely with scientists and investigators from a broad customer base. It is expected that the Sr. Research Associate will independently collect and interpret data based on project expectations, which has implications for many downstream applications, such as biomarker validation and cell and gene therapy. The SRA will also be expected to independently utilize available resources for any required troubleshooting and communicate clearly with sponsors through both electronic mail and teleconference channels. The SRA must also coordinate with internal research and development (R&D) team to learn new techniques quickly and be able to adapt to shifting priorities in a fast- paced and growing start-up environment. | 3/1/2024 |
| 3169 | ProteinSimple Minneapolis, MN Research Associate Bachelor’s degree in the biological sciences or equivalent. Exp: 0 to 2 years |
The responsibilities of this position are production, bottling, and packaging of methylcellulose, methylcellulose-containing media, and stem cell and gene therapy (SCGT) media. Perform QC testing and analysis of some methylcellulose-containing media. Perform cell culture of multiple cell lines. Production of components for additional stem cell, and non-stem cell kits. Perform additional duties as assigned. Skills used include cell culture, high attention to detail, strong communication and organizational skills. | 3/1/2024 |
| 3170 | ProteinSimple Minneapolis, MN Research Associate Bachelor’s degree in the biological sciences or equivalent. Exp: 0 to 2 years |
The responsibilities of this position are production, bottling, and packaging of methylcellulose, methylcellulose-containing media, and stem cell and gene therapy (SCGT) media. Perform QC testing and analysis of some methylcellulose-containing media. Perform cell culture of multiple cell lines. Production of components for additional stem cell, and non-stem cell kits. Perform additional duties as assigned. Skills used include cell culture, high attention to detail, strong communication and organizational skills. | 3/1/2024 |
| 3171 | ProteinSimple Minneapolis, MN Research Associate Bachelor’s degree in a related field. Exp: up to 3 years |
Are you passionate about science, an adaptable self-starter with an insatiable curiosity and have a drive to innovate and further develop your skills with a multitude of analytical tools to study and characterize biomolecules? As a Research Associate in the Analytical Services team, you will be responsible for performing routine Quality Control (QC) testing, and participating in troubleshooting efforts for released products and new products that are still in development through the application of biophysical analysis of proteins and antibodies focusing on our capillary electrophoresis systems, but may also include chromatography, immunoassays, light scattering and other analytical tools, with the aid of fully defined SOPs. You will also actively take part in group projects, participate in process improvement efforts to improve lab protocols with the goal of facilitating innovation, efficiency and productivity, and perform additional duties as assigned. | 3/1/2024 |
| 3172 | ProteinSimple Minneapolis, MN Quality Assurance Specialist B.S degree in Biology related disciplines. Exp: 0 to 5 years |
The responsibilities of this position are to engage and support various improvement projects for Document Control (Label design and document writing, routing, approval etc) and Quality Assurance activities, including but not limited to Supplier Management, Non-Conformance, CAPA and Change Management etc. | 3/1/2024 |
| 3173 | ProteinSimple Minneapolis, MN Quality Technician, Hematology QC Lab MLT/MLS degree, bachelor’s degree in biology, or related field of study. Exp: 0-1 year |
This position will require setup, maintenance, basic troubleshooting, and operation of Hematology analyzers. This position will test hematology products for homogeneity during the bottling process by following established methods. The expectation for this position is to set up and test product on all laboratory instruments and troubleshoot as necessary within 12 months of hire. This position will adhere to safety regulations. Understand the basic ISO protocols and other applicable standards. Perform additional duties as assigned. | 3/1/2024 |
| 3174 | QPS Newark, DE Associate Scientist II - Bioanalytical Dept Bachelor’s degree. Exp: 1-2 years |
As an Associate Scientist II in our Bioanalytical department, you will be a fully supervised trainee, responsible for sample preparation by various extraction methods; analysis of drug and metabolites in biological samples to support preclinical and clinical drug development programs under GLP regulations; and recording study results and observations. | 3/1/2024 |
| 3175 | QPS Newark, DE Associate Scientist I - TLM Bachelor’s Degree Biology, Molecular Biology, Biochemistry, Immunology, Pharmacology, Medical Technology, or a related field. Exp: 0+ years |
Perform routine lab operations, such as preparing reagents, pipetting, weighing, monitoring, recording, and replenishing supplies Assist supervisor in performing analysis of drug or other targets in complex biologic matrices Set-up, use and maintain complex instrumentation Document experiment details, calculations, results and observations in accordance with GLPs and SOPs Perform routine mathematical & chemical calculations | 3/1/2024 |
| 3176 | Quanterix Billerica, MA Manufacturing Associate I BS in Chemistry, Biology or related Life Sciences. Exp: 0+ years |
We are looking for an experienced and highly motivated Manufacturing Associate I located in Billerica, MA to join our Planar Manufacturing team. individual will work with a team of individuals to prepare solutions, conjugate beads, reconstitute antigens and perform filling activities to support a diverse assay menu. Hours for this position are 8am-4:30pm. | 3/1/2024 |
| 3177 | Quidel Rochester, NY Scientist I, Quality Labs BS degree in scientific or related field. Exp: 0 to 2 years |
As we continue to grow as QuidelOrtho, we are seeking a Scientist I in the Reference Laboratory. The Scientist I assures the Calibration Traceability by executing complex analytical testing of patient samples and other fluids to support the release process, stability testing, accuracy testing, and new method development. This testing uses a variety of instrumentation including, but not limited to, pH meter, manual spectrophotometers, Olympus AU400, Beckman AU480, flame photometers, atomic absorption, RIA, and HPLC. The Scientist I will maintain instrumentation, calibrates, runs quality control and analyzes requested samples. Position requires summary reports, analysis of technical data, evaluation of quality control, and instrument troubleshooting. Completion of Non-Conformance Records and/or Quality Investigations in a timely manner is required for this position. Work is scheduled, supervised, and follows established methods and procedures. Business decisions and product accuracy is dependent upon the technical ability of this individual and reproducibility of the analytical methods. This position is located on-site in Rochester, New York. | 3/1/2024 |
| 3178 | Quidel Rochester, NY Quality Analyst I (Fluid Release / Microbiology) Bachelor’s degree in Microbiology, Biology, Medical Technology, Biochemistry. Exp: 1+ years |
As we continue to grow, we are seeking Quality Analyst I to execute complex analytical testing of VITROS Calibrators, Control and other product fluids to support the formulation, release process, stability testing and accuracy of the VITROS products. This testing uses a variety of instrumentation including, but not limited to, VITROS 5,1 Chemistry System, pH meter, Chloride meter, conductivity meter and manual spectrophotometers. Will maintain VITROS instrumentation, calibrates, run quality control and analyze requested samples. In addition to support as a floater the Microbiology Laboratory testing. Works under the guidance of senior laboratory staff and management to resolve routine to complex analytical quality issues, assist in laboratory investigations and assures the product performance meets specification and claims. This position is located in Rochester, NY. | 3/1/2024 |
| 3179 | Quidel Athens, OH QC Technician II Bachelor’s degree in Chemistry, Biology, Life Science or similar discipline. Exp: 1-3 years |
The Quality Control Technician II is primarily responsible for performing Quality Control testing products at various stages of Production, as well as occasional basic technical tasks such as document control, maintenance of work areas and may perform inventory control. The QC Technician II will be expected to maintain proficiency in all areas such that re-assignment will be seamless when there are changes to workload and/or company focus. This role is located in Athens, Ohio. | 3/1/2024 |
| 3180 | Reckitt Benckiser Pharmaceutical Montvale, NJ R&D Microbiology Lab Scientist/Assistant, Equity, Claims, Compliance Bachelors Degree in a Biological Science (with microbiology focus preferred). Exp: 6 months to 2 years. |
• Conduct disinfection and sanitization efficacy tests (e.g. AOAC, ASTM, CEN,) to evaluate the antimicrobial efficacy of experimental formulations, finished products and ingredients. • Conduct required stability tests (preservative challenge tests, microbial limits) for personal care product development and launch support. • Help create new microbiological methods to foster a pipeline of innovative claims. • Manage multiple projects and provide microbiological support within the required project timelines (including testing and reporting of results) to various project teams. • Act as a subject matter expert in Microbiology. • Work with external partners in a professional and productive manner. • Perform appropriate laboratory practices and procedures, and consistently maintain laboratory records and notebooks in compliance with Good Laboratory Practice standards. • Review/author existing laboratory Standard Operating Procedures and apply them to lab and testing responsibilities. • A solid understanding of microbiology and techniques used for isolating, growing and identifying bacteria. Propagation and maintenance of appropriate microbial stocks. | 3/1/2024 |
| 3181 | Reckitt Benckiser Pharmaceutical Montvale, NJ R&D Assistant, Chemistry and Measurement Sciences- Analytical BS/BA in Chemistry or related field. Exp: 0-2 years |
Reckitt Research and Development CMS (Montvale, NJ) is seeking a self-motivated analytical chemist to join our team in the role of Assistant in the Analytical lab. The successful candidate would work independently with supervision in the lab, supporting analytical measurement for Health & Hygiene global new product development, including the Lysol, Dettol, and Harpic brands. | 3/1/2024 |
| 3182 | Reaction Biology Malvern, PA Research Associate I Bachelor of science degree. Exp: 1+ years |
To provide ground level lab work following standard protocols according to department needs. The employee will support other team members in the execution of routine lab procedures, as well as to help sustain the functionality of the lab through regular cleaning, stocking inventory, and maintenance. | 3/1/2024 |
| 3183 | Reata Pharmaceuticals Research Triangle Park, NC Manufacturing Associate (Recent Grad/Entry Level) – Upstream & Downstream Bachelor’s Degree (STEM preferred) OR BioWork Certificate or Associate’s Degree. Exp: 1+ years |
Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; with two main areas/disciplines – Upstream (Cell Culture) and Downstream (Purification). MAs perform these critical steps within Current Good Manufacturing Practice (cGMP) biosafety cabinets and cleanroom suites. | 3/1/2024 |
| 3184 | Reata Pharmaceuticals Research Triangle Park, NC Associate II, QA - Swing Shift Bachelor’s degree preferably in a field of science or biotechnology. Exp: 0-2 years |
The Quality Assurance Associate II is responsible for contributing to the oversight of key strategic, tactical, and operational aspects within Quality Assurance at the Biogen Research Triangle Park (RTP) facility. Activities include but are not limited to: review of GMP raw data for compliance, review of GMP documentation to support batch disposition, review/approval of GMP procedures, protocols and reports, GxP Quality systems-related training, identifying gaps in existing Quality systems and proposing solutions to site management. The QA Associate will perform all duties in a manner consistent with site and corporate policies, cGMP, safety, environmental and human resources policies and procedures and also adhere to all regulatory licenses and regulations, interfacing with key Quality and manufacturing customers, and coordination of investigations impacting the RTP site. The QA Associate may participate in internal compliance audits; assess and approve discrepancies from site, corporate, and regulatory guidance. The QA Associate will also ensure compliance with training policies. Please note that this is a Swing Shift position and will work a traditional 2-2-3 Manufacturing Rotation from 12pm to 12am, on a 12hr/shift schedule. There is a 10% pay differential for this position. | 3/1/2024 |
| 3185 | Reata Pharmaceuticals Research Triangle Park, NC Associate II, Quality Assurance Bachelor’s degree preferably in a field of science or biotechnology. Exp: 0-2 years |
The Associate II, Quality Assurance is responsible for contributing to the oversight of key strategic, tactical, and operational aspects within Quality Assurance at the Biogen Research Triangle Park (RTP) facility. Activities include but are not limited to review of GMP raw data for compliance, review of GMP documentation to support batch disposition, review/approval of GMP procedures, protocols and reports, GxP Quality systems-related training, identify gaps in existing Quality systems and propose solutions to site management. | 3/1/2024 |
| 3186 | R&D Systems Minneapolis, MN Advanced Manufacturing Technician Bachelor degree. Exp: 1-3 year |
The responsibilities of a Manufacturing Technician are to support the laboratory staff with the process of building and manufacturing science products. This position will perform a variety of tasks within a laboratory setting that may include labeling, recording data, operating equipment, formulation and plate coating. | 3/1/2024 |
| 3187 | R&D Systems Wallingford, CT Research Associate, Reagent Manufacturing Bachelors’ Degree in Biology, Chemistry, Biochemistry or related biological science. Exp: 1+ years |
The candidate will be responsible for providing accurate, efficient and quality production tasks in a cutting-edge molecular biology laboratory. The individual must exhibit a high degree of attention to detail and follow multi-step complicated technical protocols and processes accurately and rapidly. A basic molecular biology or biochemistry laboratory skill set is required as is experience in the use and maintenance of multiple types of biological instrumentation and systems. This position requires the ability to function with minimal oversight and convert customer demands into finished product. The individual will execute production protocols and ensure continual operation of equipment to meet production targets assigned by management, effectively and immediately communicate any complications that arise during manufacturing, and then be able to work across teams to establish and maintain a solution and provide detailed documentation of manufacturing activities, on a daily basis. | 3/1/2024 |
| 3188 | R&D Systems Minneapolis, MN Senior Manufacturing Technician Bachelor’s Degree in Science or Engineering. Exp: 1+ years |
The responsibilities of this position are to organize and stage different types of vials and bottles for filling. The position requires that the candidate has the ability to fill antibodies and protein solutions into vials. The candidate may be required to perform calculations based on volume and purity. The candidate must have the ability to cap and label vials of antibodies and proteins quickly and accurately. The candidate will be required to complete computer inventory entries and track supplies accurately. The candidate must have the ability to work in a laminar flow hood and fill (pipetting) products for extended periods of time. The candidate must have the ability to inspect vials with product and identify defects. The candidate will be required to operate cap torqueing and labeling automation. The candidate's ability to trouble shoot automation is an added skill set that would be desirable. The candidate will be required to learn nationalization process. The candidates' ability to complete paperwork accurately is critical. The candidate's ability to work in a fast-paced regulatory environment as a team is critical. The candidate must have the ability to gown and work in a clean room. The candidate performs pipette calibration accurately. The candidate may work on new production introduction, implementation, and filling. The candidate will help with yearend inventory counting and perform additional duties as assigned. The candidate will be required to exhibit EPIC behaviors aligned with the corporate vision. | 3/1/2024 |
| 3189 | R&D Systems Minneapolis, MN Advanced Research Associate Master’s degree. Exp: 1+ years |
In this role, you would be responsible for the development and execution of QC test method validations for a variety of products, utilizing a wide variety of laboratory techniques such as cell culture, flow cytometry, qPCR, and other analytical methods. This position also assists in troubleshooting investigations and process improvement projects. As an Advanced Research Associate, you will also participate in cross-functional teams focused on new product introduction. | 3/1/2024 |
| 3190 | Roche Seattle, WA Lab Assistant BS in Chemistry, Biochemistry, Biology or related field. Exp: 1+ years |
Roche Diagnostics acquired Stratos Genomics (SBX Nanopore Sequencing) in 2020 for its novel Sequencing by eXpansion (SBX™) technology. SBX™ uses unique applications from chemistry, biochemistry, and protein engineering to sequence DNA by nanopore in rapid time with high accuracy and low cost. We are looking for people who are excited to collaborate with us to make SBX successful. You will join the SBX Central Services team of Lab Assistants and play a crucial role in the day-to-day operations of the lab. | 3/1/2024 |
| 3191 | Nexus Pharmaceuticals Lincolnshire, IL Quality Control Chemist I BS or MS in chemistry or related field with a minimum of 20 hours of chemistry coursework. Exp: one year |
The Quality Control Chemist I is responsible for the execution of wet chemistry and analytical chemistry techniques during testing of Raw Materials and finished products. This testing includes: Instrumental analysis such as HPLC, GC, UV and FTIR as well as wet chemistry such as titrations, LOD and chemical identification tests. The Quality Control Chemist I performs method development or method transfer testing. The Quality Control Chemist I works in the laboratory in a safe and effective manner. | 2/20/2024 |
| 3192 | Nostrum Laboratories Bryan, OH Chemist I Bachelors Degree. Exp: 0 - 4 years |
Responsible for development and validation of analytical methods in support of product development and IND/NDA/ANDA filings. Perform routine wet chemical and instrumental analysis on raw materials, in-process, finished and stability products. Accurately compiles and reports data. Gather, compile and compose documents needed for regulatory submissions. | 2/20/2024 |
| 3193 | Nostrum Laboratories Bryan, OH QC LAB TECHNICIAN I Associates Degree. Exp: 1-2 years |
The QC Technician I is responsible for conducting non-complex analytical tests for raw materials, components, in-process materials, finished products, other samples as assigned, in accordance with cGMP regulations, regulatory filings, and approved procedures. | 2/20/2024 |
| 3194 | Novartis Cambridge, MA Research Scientist II, Cell Pharmacology – CVM MS degree in biochemistry, molecular or cell biology, biophysics, biomedical engineering or a related field. Exp: 0+ years |
We are seeking a highly motivated Research Scientist II to join our Cell Pharmacology team. You will advance our understanding of disease biology, contribute to target identification efforts, and work towards the discovery and optimization of new drugs for The Cardiovascular and Metabolic Disease Area (CVM) of Biomedical Research. The work involves collaboration with research scientists across multiple disciplines as well as translational medicine colleagues who support bringing our drugs to patients. | 2/22/2024 |
| 3195 | Novartis San Diego, CA Research Scientist II, CGT Biodistribution and Technology Scientific background with an BS in Biological Sciences or a closely related discipline. Masters preferred. Exp: 1+ years |
We are seeking a highly motivated scientist to contribute to gene therapy development as part of the global community of investigators in the Cell & Gene Therapy (CGT) group within BRC. The successful candidate will work at the cutting edge of gene therapy biodistribution, platform and technology research to model and test priorities in translational research. The successful candidate will be a collaborative scientist experienced in molecular biology experiments, liquid handling automation and/or NGS sequencing. | 2/22/2024 |
| 3196 | Novartis Emeryville, CA Research Scientist, Comparative Medicine Bachelor’s degree (B.A./B.S.) in animal or life sciences field preferred. Exp: 1+ years |
Comparative Medicine (CM) provides high quality husbandry and in vivo research work and support to enable drug discovery research and development. We are looking for a Research Scientist in CM to provide husbandry and vivarium Operations support, and to help run in vivo research studies and projects to support the diverse and exciting project portfolio at GH. The candidate should be action-oriented, Experienced with rodent husbandry and vivarium operations, skilled in in vivo procedures used to perform in vivo experiments with high technical and ethical standards and provide best in class animal care. The role will require an ability to work independently as well as in close collaboration with other CM colleagues, research scientists, the IACUC and animal welfare team. | 2/22/2024 |
| 3197 | Novartis Morris Plains, NJ Associate Scientist (Hours: Wed - Sat 7am - 5:30pm) BA or MS in chemistry, biochemistry, microbiology, or other related science. Exp: 0 - 5 years |
Under general direction, perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay, and raw materials, as appropriate). | 2/22/2024 |
| 3198 | Novartis Morris Plains, NJ Associate Scientist (Hours: Wed - Sat 2:30pm - 1:00am) BA or MS in chemistry, biochemistry, microbiology, or other related science Exp: 0 - 5 years |
Under general direction, perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay, and raw materials, as appropriate). | 2/22/2024 |
| 3199 | Novo Nordisk Durham, NC Manufacturing Operator I - Future 2nd Shift Associate’s degree preferred. Exp: one (1) year |
Efficiently, effectively & safely clean, setup & operate manufacturing equipment to achieve production goals, while adhering to applicable cGMPs & SOPs. | 2/22/2024 |
| 3200 | Novo Nordisk West Lebanon, NH Manufacturing Science and Analytical Technology Associate I Bachelor’s degree or equivalent in Biochemistry, Chemistry, Engineering or a closely related field. Exp: one year |
This position has the responsibility of working with senior level Scientists to execute laboratory scale process development or validation studies in support of process or assay development, or process troubleshooting or scale-up. The scientific knowledge in this position will range from familiarity with details of manufacturing process, process chemistries, development studies and relevant assay methods and instruments. This position will be one of the interfaces between MSAT and Manufacturing or Quality. | 2/22/2024 |
| 3201 | Novo Nordisk Clayton, NC Associate Process Engineer - FP - TECH SUPPORT - Assembly - Nights - Team C Bachelor’s degree in Chemical Engineer, Mechanical Engineering, or related discipline. Exp: One (1) year |
Responsible for assisting with design and implementation of manufacturing processes, instrumentation and equipment start-ups from the laboratory through manufacturing scale. | 2/22/2024 |
| 3202 | Novo Nordisk West Lebanon, NH Manufacturing Technician- Night Shift Bachelors’ Degree in a science discipline. Exp: zero (0) years’ |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. | 2/22/2024 |
| 3203 | Novo Nordisk Durham, NC Maintenance Technician I - 2nd Shift AA/AS/AAS degree from an accredited university in a relevant field required. Exp: one (1) year |
Improve systems & equipment reliability on assigned process, reduce system/equipment downtime on assigned process & support operation of assigned process. | 2/22/2024 |
| 3204 | Noxilizer Hanover, MD Research and Development Laboratory Scientist Bachelor’s degree in Biology, Biotechnology, Biomedical Engineer, Material Science or related field preferred. Exp: 1 year |
The R&D Lab Scientist is responsible for performing, documenting and reporting microbiological sterilization studies for Noxilizer’s customers. Noxilizer’s customers range from Fortune 500 pharmaceutical, biotech and medical device companies to start-ups that are in the US, Europe and Asia. These studies are the first critical step in the customer’s evaluation of nitrogen dioxide sterilization and their product, as well as an important revenue-generating area for the company. The R&D Laboratory Scientist will join a high-performing team of experts to solve sterilization challenges while they grow their skills for future career opportunities. | 2/22/2024 |
| 3205 | NxStage Ogden, UT Biocompatibility Engineer I Bachelor's Degree in related Engineering or scientific discipline required. Exp: 0 - 2 years' |
The entry level Engineer will participate in designing, executing, and championing research and development activities of Fresenius' products. As a member of a tech team, the Engineer I environment is mentored - with oversight from higher level Engineers to complete pre-defined work. The Engineer I may be involved in quality planning, internal audits, data collection and analysis, specification development and review and design review and qualification. The Engineer I will work with cross-functional teams to develop, commercialize, and maintain high quality. | 2/23/2024 |
| 3206 | NxStage Southaven, MS Medical Lab Scientist - Microbiology Bachelor's Degree in Medical Laboratory Sciences or Biological Sciences required. Exp: 0 - 3 years' |
Performs a wide variety of moderately and highly complex tasks and analysis of human fluids and tissues, using manual procedures as well as operating various laboratory equipment and automated analyzer systems. Responsible for acceptable quality control accurate testing, and release of accurate patient results in collaboration with the Lead, Supervisor or Manager. | 2/23/2024 |
| 3207 | NxStage Rockleigh, NJ Medical Lab Scientist - Diagnostic Immunology Bachelor’s Degree in Medical Laboratory Sciences or Biological Sciences required. Exp: 0 – 3 years’ |
Performs a wide variety of moderately and highly complex tasks and analysis of human fluids and tissues, using manual procedures as well as operating various laboratory equipment and automated analyzer systems. Responsible for acceptable quality control accurate testing, and release of accurate patient results in collaboration with the Lead, Supervisor or Manager. | 2/23/2024 |
| 3208 | NxStage Southaven, MS Medical Lab Scientist - Hematology Bachelor’s Degree in Medical Laboratory Sciences or Biological Sciences required. Exp: 0 – 3 years’ |
Performs a wide variety of moderately and highly complex tasks and analysis of human fluids and tissues, using manual procedures as well as operating various laboratory equipment and automated analyzer systems. Responsible for acceptable quality control accurate testing, and release of accurate patient results in collaboration with the Lead, Supervisor or Manager. | 2/23/2024 |
| 3209 | NxStage Mesa, AZ Biomedical Equipment Technician Associate Degree in electronics / biomedical technology, or equivalent a plus. Exp: 0 – 1 year |
Entry level position focuses on the development of Knowledge, Skills, and Abilities (KSA) in a supervised environment with the intent of developing performance and effective, efficient independent functioning under close supervision upon completion of various training processes over time. Under close supervision and consistent with completed training and qualifications, schedules and performs routine repair and maintenance activities of medical equipment, water systems and the physical plant in assigned facilities that ensures patient safety and staff operating equipment in accordance with company policies and procedures, manufacturer’s documentation, industry standards and local, state and federal regulatory requirements. Responsible for efficient use of resources related to repair and maintenance costs. | 2/23/2024 |
| 3210 | NxStage Richmond, VA Biomedical Equipment Technician Associate Degree in electronics / biomedical technology, or equivalent a plus. Exp: 0 – 1 year |
Entry level position focuses on the development of Knowledge, Skills, and Abilities (KSA) in a supervised environment with the intent of developing performance and effective, efficient independent functioning under close supervision upon completion of various training processes over time. Under close supervision and consistent with completed training and qualifications, schedules and performs routine repair and maintenance activities of medical equipment, water systems and the physical plant in assigned facilities that ensures patient safety and staff operating equipment in accordance with company policies and procedures, manufacturer’s documentation, industry standards and local, state and federal regulatory requirements. Responsible for efficient use of resources related to repair and maintenance costs. | 2/23/2024 |
| 3211 | NxStage Saint Peters, MO Biomedical Equipment Technician Associate Degree in electronics / biomedical technology, or equivalent a plus. Exp: 0 – 1 year |
Entry level position focuses on the development of Knowledge, Skills, and Abilities (KSA) in a supervised environment with the intent of developing performance and effective, efficient independent functioning under close supervision upon completion of various training processes over time. Under close supervision and consistent with completed training and qualifications, schedules and performs routine repair and maintenance activities of medical equipment, water systems and the physical plant in assigned facilities that ensures patient safety and staff operating equipment in accordance with company policies and procedures, manufacturer’s documentation, industry standards and local, state and federal regulatory requirements. Responsible for efficient use of resources related to repair and maintenance costs. | 2/23/2024 |
| 3212 | Ocean Ridge Biosciences Exton, PA Lab Assistant Associate or bachelor’s degree preferred. Exp: 1+ years |
The Lab Assistant will work under the supervision of laboratory staff or researchers to assist in the smooth functioning of laboratory operations. This role involves a combination of technical and administrative tasks to support ongoing laboratory activities and required documentation. Additionally, the Lab Assistant will provide crucial support for clinical trial kitting activities and sample receipt. | 2/23/2024 |
| 3213 | Ocean Ridge Biosciences Chicago, IL Assistant/Associate Toxicologist BS degree in animal/veterinary science, biology, or related disciplines. Exp: Assoc: 0-3 years |
The Associate/Assistant Toxicologist plays a key, hands on role in the conduct of preclinical studies and supports the Study Director to ensure that Sponsor studies are conducted properly and according to FDA guidelines. | 2/23/2024 |
| 3214 | Ocean Ridge Biosciences Hayward, CA Research Associate M.S. degree in related scientific discipline. Exp: 0-3 years |
1) Perform Watson design according to Study Protocols 2) Conduct basic method development and validation studies. 3) Ability to troubleshoot and solve basic technical and instrumental issues. 4) Conducts and documents work in a regulated environment. 5) Reviews the data package and notebooks for junior chemists 6)Writing up analytical methods, protocols, and reports under supervision 7) Perform project communication with client, study director, and project management team under supervision | 2/23/2024 |
| 3215 | Ocean Ridge Biosciences Exton, PA Associate Scientist/Scientist Scientist: M.S.; Associate Scientist: B.S./B.A. Exp: Scientist: 1-5 years; Associate Scientist: 1-5 years |
This is a technical scientific position within the Biologics Service Team. The Biologics Service Team is responsible for conducting bioanalytical methods related to large molecule biotherapeutic drug development across all therapeutic areas, spanning nonclinical studies to post-market clinical development. | 2/23/2024 |
| 3216 | Ocean Ridge Biosciences Exton, PA Lab Technician High School diploma, associate degree, or bachelor’s degree. Exp: 0-2+ years |
Frontage Laboratories, Inc. is hiring a Laboratory Technician I/II in the CMC Analytical Services division. The Laboratory Technician is responsible for supporting scientists in laboratory testing activities. The Laboratory Technician’s duties include following procedures, recording data, working with laboratory equipment, ordering supplies, and maintaining an inspection ready work environment. | 2/23/2024 |
| 3217 | Ocean Ridge Biosciences Exton, PA Lab Technician Bachelor’s degree in molecular biology, Biology, Biochemistry, Chemical Engineering, Mechanical Engineering, or equivalent. Exp: 1-5 years |
We are looking for a qualified Lab Technician to join our team. The role will perform and support laboratory procedures and controls within Biologics, Gene, and Cell Therapy (BGC) Department to maintain efficiency and compliance for the laboratory. The ideal candidate needs to have an entrepreneurial spirit that enables her/him to wear multiple hats as we scale-up the laboratory business. The candidate will have experience in working in a laboratory environment, preferably within biologics/or GCT lab. The candidate will be well-trained to maintain safety conditions in the lab and expected to be passionate in working in a matrix organization environment. The goal is to optimize lab compliance and maintaining the smooth running of the lab. | 2/23/2024 |
| 3218 | Ocean Ridge Biosciences Exton, PA Associate Scientist Bachelor’s or master’s degree in molecular biology, cell biology, biochemistry, or a related field. Exp: 1+ years |
The Cell-based Assay Core Lab, based at our Exton headquarters, stands as a premier provider of diverse cell-based assays. These include potency assays, neutralizing antibodies assays, EliSpot, virus plaque assay, TCID50 Assays etc. We are seeking a candidate with a fundamental understanding of Cell Biology, Biochemistry, and Molecular Biology. The ideal candidate should be highly organized, self-motivated, enthusiastic about learning, and capable of managing multiple projects concurrently | 2/23/2024 |
| 3219 | Ocular Therapeutix Bedford, MA Manufacturing Operator Associate degree or biotechnology certificate strongly preferred. Exp: 1-3 years |
The Manufacturing Operator is responsible for performing all manufacturing processes related to the Ocular Therapeutix’s products. The Operator is an integral part of our team and will be responsible for manufacturing activities by following appropriate SOP(s) and supervisor direction, in accordance with current good manufacturing practices and company policy and procedures. | 2/23/2024 |
| 3220 | Ocular Therapeutix Bedford, MA Device Engineer I Bachelor’s degree (in Mechanical Engineering, Biomedical Engineering or related discipline. Exp: 0 - 2 yrs |
We are seeking a motivated engineer to join the Product Development team. The individual is responsible for contributing to the design and manufacture of injectors and applicators used for the delivery of hydrogel drug product to treat various ophthalmic conditions. Responsibilities include product design (CAD modeling), design verification, design validation and other elements of Design Control. The role also includes process development activities, line layout, fixture design, equipment procurement, and supporting GMP manufacturing of clinical trial material. This individual will participate in defining voice of the customer requirements and product and material specifications. They will also perform risk analysis activities and design verification testing. This role will require a mix of cross-functional collaboration as well as execution of key laboratory experiments to achieve program objectives. The position is set in a dynamic and fast-paced environment. Critical areas of immediate focus include planning and execution of laboratory experiments, CAD design and maintenance of engineering drawings, Design for Manufacturability, process development and incorporation of fixture design and semi-automated processes to support development of manufacturing processes for late-stage clinical production that are capable, scalable, and sufficiently robust for transfer to commercial manufacturing. We are seeking a motivated engineer to join the Product Development team. The individual is responsible for contributing to the design and manufacture of injectors and applicators used for the delivery of hydrogel drug product to treat various ophthalmic conditions. Responsibilities include product design (CAD modeling), design verification, design validation and other elements of Design Control. The role also includes pr | 2/23/2024 |
| 3221 | OriGen Biomedical Austin, TX Manufacturing Engineer I Bachelor’s degree in Engineering. Exp: 0-2 years’ |
The Manufacturing Engineer I will evaluate and develop processes to ensure quality, cost, and efficiency requirements are met. S/he will troubleshoot problems with production and take corrective actions and will research and make recommendations on the purchase of equipment and/or upgrades to existing equipment and support manufacturing as needed. | 2/23/2024 |
| 3222 | Parexel West Point , PA Scientist II - Microbiologist Bachelor’s degree required; concentration in a scientific or applied discipline strongly preferred. Exp: 1-2 years |
We are looking to fill a Scientist 2 position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients in West Point, PA. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer any sponsorship. | 2/23/2024 |
| 3223 | Parexel Rahway, NJ Scientist 3 - Drug Product Microbiologist Bachelor’s degree required; concentration in a scientific or applied discipline strongly preferred. Exp: 1-2 years |
We are looking to fill a microbiologist position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients in Rahway, NJ. | 2/23/2024 |
| 3224 | Parexel Rahway, NJ Crystallization Engineer III MS degree or equivalent in Engineering, Chemistry, Chemical Engineering, or a related field is required. Exp: 1-2 years’ |
We are looking to fill an Engineer 3 position working as a full-time employee of Parexel on long-term assignment onsite at one of our clients in Rahway, NJ. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer any sponsorship. Overview / Responsibilities The Chemical Engineering Research and Development department of one of our clients in Rahway, NJ has a position available that will have primary accountability for lab process development specifically around API crystallization, isolation, drying, and particle physical attribute control. Activities will include working with gram quantities at the bench scale to a few kilograms at the Unit Operations and Preplab scales utilizing wet and dry processing equipment within these labs (e.g., crystallization vessels, filtration and drying equipment, and wet and dry milling tools, etc.). The department offers fast-paced, hands-on research that requires a high degree of technical skills and contributions. Secondary activities may include experiments and the use of instruments associated with process safety evaluation when needed, and the general support of Specialty Labs operations within the Chemical Engineering R&D Department. | 2/23/2024 |
| 3225 | Par Pharmaceutical Rochester, MI Microbiologist I Bachelor of Science degree in microbiology, biology or related field with microbiology coursework required. Exp: 1+ years |
Performs Quality laboratory microbiological analyses of materials including water testing, finished product testing, raw material testing, and method validation. Supports laboratory investigations of moderate scope and complexity while abiding by GMPs and GLPs. Has working knowledge of, and stays current with, regulatory guidance and compendia relevant to laboratories and pharmaceutical manufacturing. | 2/23/2024 |
| 3226 | Par Pharmaceutical Horsham, PA Associate Scientist, Bioprocess Technical Operations Bachelor’s degree in a biological, chemical, or related discipline is required. Exp: 1+ years |
The Associate Scientist will perform lab duties under the direct supervision of senior Biotech Ops (BTO) staff. Key areas of focus/support include preparation of buffers as well as execution of one or two specific methods or processes. | 2/23/2024 |
| 3227 | Par Pharmaceutical Rochester, MI Quality Associate Specialist, Product Release (Afternoon Shift) BA/BS degree in a related discipline. Exp: 0-1 year |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. | 2/23/2024 |
| 3228 | Partner Therapeutics Lynnwood, WA Quality Control Lab Support Technician I (Contract/Onsite) B.S. or equivalent degree in science (Biology, Chemistry, Biochemistry, etc.) or related field (Chemical Engineering, etc.) strongly preferred. Exp: 1 year |
The Quality Control Department is responsible for all testing related to the manufacturing and release of Leukine which includes testing raw materials, process intermediates, Bulk Drug Substance (“BDS”), and Drug Product (“DP”). The Lab Support Technician I role is an individual contributor who maintains and prepares the onsite laboratories to perform required testing. This position is an ONSITE role requiring a presence 5 days per week at our Lynnwood, WA plant which is a cGMP production scale manufacturing facility for our product, Leukine® (sargramostim), a therapeutic glycoprotein. | 2/23/2024 |
| 3229 | Partner Therapeutics Lynnwood, WA Quality Control Lab Support Technician I (Onsite) B.S. or equivalent degree in science (Biology, Chemistry, Biochemistry, etc.) or related field (Chemical Engineering, etc.) strongly preferred. Exp: 1 year |
The Quality Control Department is responsible for all testing related to the manufacturing and release of Leukine which includes testing raw materials, process intermediates, Bulk Drug Substance (“BDS”), and Drug Product (“DP”). The Lab Support Technician I role is an individual contributor who maintains and prepares the onsite laboratories to perform required testing. This position is an ONSITE role requiring a presence 5 days per week at our Lynnwood, WA plant which is a cGMP production scale manufacturing facility for our product, Leukine® (sargramostim), a therapeutic glycoprotein. | 2/23/2024 |
| 3230 | PeproTech St. Louis, MO Lab Technician II-Formulations Associate’s degree in science field or or Bachelor’s degree in science or engineering field. Exp: AS: 1+ years; BS: 0+ years |
The candidate will be responsible for the performance of operations in support of the BPS Cell Culture Development Team. You will carry out a variety of functions related to Upstream Process Development operations with primary focus on medium and buffer formulations. Additional functions may include but are not limited to activities such as supply stocking and organization, and equipment maintenance including basic troubleshooting, cleaning, and performance maintenance on supporting equipment. | 2/23/2024 |
| 3231 | Merieux NutriSciences Minnetonka, MN Microbiology Lab Tech Associate's degree in STEM degree preferred. Exp: 1+ year |
We are looking for a Microbiology Lab Tech in 11585 K-Tel Dr, Minnetonka, MN 55343 USA. Your mission will be to: Purpose (Objective): The incumbent prepares sample for processing and maintains documentation of process to facilitate analysis procedures. | 2/12/2024 |
| 3232 | Merieux NutriSciences Stone Mountain, GA Microbiology Laboratory Technician Associates degree or equivalent work experience. Exp: 1+ year |
We are looking for a Microbiology Laboratory Technician in 2169 West Park Court, Stone Mountain, GA 30087 USA. Your mission will be to: Purpose (Objective):The incumbent prepares samples for processing and maintains documentation of process to facilitate testing procedures. | 2/12/2024 |
| 3233 | Merieux NutriSciences Salt Lake City, UT Chemistry Technician Associates degree or Bachelors degree. Exp: AS: 1+ years; BS: 0+ years |
We are looking for a Chemistry Technician in 1945 Fremont Drive, Salt Lake City, UT 84104 USA. Your mission will be to: Composting and grinding of samples for analysis as required. Perform chemical analyses such as protein, moisture, fat, ash, and other components. Prepare sample for analysis according to procedure. Retrieve samples from designated areas (e.g. log-in, sample storage). Perform chemical analyses of macronutrients, micronutrients or other parameters as designated. Extract desired component from sample with appropriate processes so that concentration can be determined. Prepare standards and reagents that are needed for the analysis procedure. Write/label all samples throughout the process so that Client and sample numbers can be tracked. Perform calculations, checking and interpretation of results where applicable. Track status of designated tests as assigned to ensure Client turn around time commitments are met and inform supervisor of non compliance. Assist other departmental personnel with analysis tasks so that testing can proceed according to specified time limits. | 2/12/2024 |
| 3234 | Merieux NutriSciences Minnetonka, MN Media Technician Associate's degree in STEM degree preferred. Exp: 1+ years |
We are looking for a Media Technician in 11585 K-Tel Dr, Minnetonka, MN 55343 USA. Your mission will be to: Purpose (Objective): The incumbent prepares sample for processing and maintains documentation of process to facilitate analysis procedures. | 2/12/2024 |
| 3235 | Merieux NutriSciences Springfield, MO Microbiologist I Associates degree required, Bachelors preferred or equivalent work experience. Exp: One (1)- 2 years |
We are looking for a Microbiologist I in 2835 N Oak Grove, Springfield, MO 65803 USA. Your mission will be to: Purpose (Objective): The incumbent is responsible for the testing of samples using various microbiological analyses. The incumbent provides analytical support for the lab by ensuring that laboratory procedures are being performed within specified quality guidelines. This position serves as a technical resource and provides ongoing technical support related to method and process implementations. This position spends the majority of time or all of their time in diagnostics. Schedule is 11:30-8p, Tuesday-Saturday. | 2/12/2024 |
| 3236 | Merieux NutriSciences Crete, IL Microbiologist III Masters degree. Exp: 1-2 years |
We are looking for a Microbiologist III in 3600 Eagle Nest Dr, North Building, Crete, IL 60417 USA. Your mission will be to: The incumbent is responsible for the testing of food samples using various microbiological analyses. The incumbent provides analytical support for the lab by ensuring that laboratory procedures are being performed within specified quality guidelines. This position serves as a technical resource and provides ongoing technical support related to method and process implementations. This position spends the majority of time or all of their time in diagnostics. | 2/12/2024 |
| 3237 | Merieux NutriSciences Gainesville, FL Microbiology Lab Technician Associates degree. Exp: 0+ years |
We are looking for a Microbiology Lab Technician in 2183 SE Hawthorne Rd, Gainesville, FL 32641 USA. Purpose (Objective):The incumbent prepares samples for processing and maintains documentation of process to facilitate testing procedures. | 2/12/2024 |
| 3238 | Meso Scale Discovery Gaithersburg, MD Research Associate Bachelor’s degree in life sciences, or related area is required. Master’s degree a plus. Exp: 1+ years |
This position is responsible for executing experiments and analyzing the resulting data in support of reagent and assay development projects with close supervision. This is a laboratory-based position responsible for advancing research and/or development objectives focused on leading-edge biomarker measurements and technology. | 2/12/2024 |
| 3239 | Meso Scale Discovery Rockville, MD Product Transfer Associate I Bachelor degree in Biology, Chemistry, Biotechnology, Engineering or related field, or associate’s degree with equivalent experience. Exp: One year |
This position is responsible for manufacturing assay kit components during development phases, meeting production schedules and troubleshooting. The role is cross-disciplinary and requires coordination across multiple departments (Operations, Quality, Research & Development, etc). | 2/12/2024 |
| 3240 | Microbiologics Saint Cloud, MN Quality Control Technician Four-year microbiology or related degree required. Exp: 1+ years |
We are currently looking to add a Quality Control Lab Technician to our St. Cloud, MN team. In this role, you will perform Quality Control Testing, Shelf-Life Testing, and Packaging Event Evaluations on Microbiologics products in accordance with the appropriate Company Device Master Record (DMR), policies and procedures with the objective to release only production products that meet all of Microbiologics acceptance criteria. | 2/12/2024 |
| 3241 | Microbiologics Lexington, KY Microbial Production Technician Bachelor’s degree in Biology, Microbiology or closely related field. Exp: 0+ years |
We are currently looking to add a Microbial Production Technician to our team in Lexington, KY. In this role, you will be responsible for manufacturing of microorganism product line, fungal serology, proficiency materials, and custom and retail products, in addition to other duties listed below. | 2/12/2024 |
| 3242 | Microbiologics Saint Cloud, MN Research & Development Technician Four (4) year degree in relevant field (e.g., biology, microbiology, virology, cell biology molecular biology). Exp: 1+ years |
We are currently looking to add a R&D Technician to our team in Research & Development. In this role you will be responsible for assisting with supervised experiments using microbiology and molecular biology techniques and/or cell culture and virology techniques as well as other applicable methodologies leading to new products or process improvements. | 2/12/2024 |
| 3243 | Mirati Therapeutics Summit West, NJ Specialist, QA Engineering Bachelor of Science degree required. Exp: 1 year |
The Specialist is responsible for providing quality oversight for Site Validation activities and Quality Control Laboratory method and equipment validation in accordance with BMS policies, standards, procedures and Global cGMP. Functional responsibilities for the incumbent include ensuring accurate and timely maintenance and review of validation and qualification documents for all equipment, laboratory, and facility activities; support data integrity initiatives for the site. | 2/15/2024 |
| 3244 | Mirati Therapeutics Devens, MA Specialist, Validation Engineer I, Cleaning Validation Knowledge of Engineering and Quality Assurance generally attained through studies resulting in a B.S., in engineering, a related discipline. Exp: 0-2 years |
Supports the design and maintenance of a robust cleaning validation lifecycle for process equipment and systems, that includes a bench-scale cleaning program, a cleaning monitoring program, and a cleaning verification changeover program for a fully automated, multi-product biologics manufacturing facility. Performs cleaning validation lifecycle activities, including work arising from change controls, capital projects, shutdown/changeover activities, cleaning validation bench-scale studies, and cleaning monitoring programs. Works collaboratively with peers within Validation, Manufacturing Systems, Information Technology, Manufacturing, Manufacturing Engineering and Quality Effectively manages workload to address priorities, meet schedules, maximize productivity, reduce costs, and increase efficiencies. Ensures alignment with site validation master plans and philosophies, BMS policies, and industry guidelines on validation and quality engineering. | 2/15/2024 |
| 3245 | Miromatrix Medical Woburn, MA Research Associate I, Cell Production and Tissue Engineering Bachelor’s Degree in cellular biology, developmental biology, biomedical engineering, or a related field. Exp: 1+ years |
The Research Associate I is responsible for helping to derive and expand the necessary cell types to develop and build autologous tissue constructs as a solution to end-stage renal disease and other disorders. This position is part of a multidisciplinary team led by experienced stem cell and developmental biologists and engineers. This individual is experienced in human primary cell and stem cell derivation, expansion, and differentiation. Technical expertise in multiple cell biology techniques including quantitative polymerase chain reaction, fluorescence microscopy, flow cytometry and other immune-based assays are critical to this position. | 2/15/2024 |
| 3246 | Miromatrix Medical Eden Prarie, MN Research Associate II/Senior Research Associate, Cell Development & Characterization Research Associate II: Master’s degree in biology, cellular and molecular biology, biomedical sciences, biomedical engineering, or biomanufacturing. Exp: 1+ years’ |
The Senior Research Associate/Associate II, Cell Development and Characterization, is responsible for performing cellular analysis of primary kidney and liver cells using flow cytometry, immunofluorescence, immunocytochemistry, and qPCR. This individual must be self-motivated with demonstrated ability to culture and characterize mammalian cells, creatively solve problems, should be excellent at troubleshooting, and able to work independently and in collaboration with a diverse team of multidisciplinary scientists and engineers diligently and carefully. This role, and team, will be tasked with characterization of kidney and liver cells for cellularization efforts in Bioengineered Organ Development, and with developing GMP level protocols and release tests in preparation of IND filing. | 2/15/2024 |
| 3247 | Moderna Therapeutics Norwood, MA Research Associate, Technical Development Operations BS in Biochemistry, Molecular Biology, or a related field. Exp: 1-2 years |
Moderna is seeking a molecular biologist to join Technical Development newly established Sequencing Center. In this laboratory-based position, the individual will routinely process sequencing samples, operate, and troubleshoot instruments including ABI 3730xl, Echo, Illumina MiSeq, NovaSeq, plate readers and liquid handlers. Experience with lab automation is a plus. The candidate must thrive in a fast pace high throughput environment, have a collaborative spirit, and be curious and willing to learn new techniques to push process development forward. | 2/16/2024 |
| 3248 | Moderna Therapeutics Norwood, MA Research Associate, Analytical Development A BS with a focus on microbial sciences. Exp: 1+ years |
We seek a motivated individual with experience in a microbiology laboratory setting to support microbial testing in Technical Development. Candidates should have experience with various microbial techniques such as aseptic sample handling, filtration and pipetting. In this laboratory-based role, the Research Associate will be responsible for supporting daily laboratory operations and following microbiology test protocols for analysis of in-process and final product bioburden and endotoxin release testing of development samples (DNA plasmid, protein, mRNA, and LNP sample types). In addition, the Candidate would contribute to method optimization, testing in support of rapid microbiological method qualifications and maintain the microbiology laboratory and equipment. | 2/16/2024 |
| 3249 | Moderna Therapeutics Norwood, MA Research Associate, Drug Product Development Masters or Bachelor’s Degree in on one of the following fields: Chemical Engineering, Biochemical or Biomedical Engineering, Pharmaceutical Sciences, Exp: 0 – 2 years |
We are seeking a highly skilled and motivated Research Associate in Drug Product Development respiratory team, to work in a team developing Moderna’s sterile drug product processes and products that enable clinical and future commercial supply. The primary role for this position will be to support product concept development including process development and scale-up work, container development and conditions of use studies. The incumbent will support the development of compositions, aseptic fill/finish unit operations through the development and use of scale-down models, process characterization studies etc. Applicants should have relevant pharmaceutical sciences related experience with various aspects of drug product development. The applicant should have exceptional ability to plan, execute and report, to communicate and collaborate, and requires strong attention to detail while working in a fast-paced, interdisciplinary environment. | 2/16/2024 |
| 3250 | Moderna Therapeutics Norwood, MA Engineer II, MST Biochemical engineer, Chemical engineer, Biochemistry or Biology background. MS. Exp: 1 to 3 years’ |
The Engineer II, MS&T will be part of Moderna’s Manufacturing Science and Technology team responsible for process implementation, technical support, and person-in-plant coverage to ensure the robust End-to-End production of our new mRNA Individualized Neoantigen Therapies (INT). The individual will work collaboratively with cross-functional stakeholders such as Technical Development, Manufacturing, Regulatory, and Quality, to ensure all technical aspects of production are successfully executed. This will be a 3rd shift role, working a Wednesday through Saturday schedule from 10:00pm until 8:00am. | 2/16/2024 |
| 3251 | Moderna Therapeutics Norwood, MA Engineer I, MS&T Biochemical engineer, Chemical engineer, Biochemistry or Biology background. BS. Exp: 1 to 2 years |
The Engineer I, MS&T will be part of Moderna’s Manufacturing Science and Technology team responsible for process implementation, technical support, and person-in-plant coverage to ensure the robust End-to-End production of our new mRNA Individualized Neoantigen Therapies (INT). The individual will work collaboratively with cross functional stakeholders such as Technical Development, Manufacturing, Regulatory, and Quality, to ensure all technical aspects of production are successfully executed. This will be a 3rd shift role, working a Sunday through Wednesday schedule from 10:00pm until 8:00am. | 2/16/2024 |
| 3252 | Moderna Therapeutics Norwood, MA Engineer I, MS&T Biochemical engineer, Chemical engineer, Biochemistry or Biology background. BS. Exp: 1 to 2 years |
The Engineer I, MS&T will be part of Moderna’s Manufacturing Science and Technology team responsible for process implementation, technical support, and person-in-plant coverage to ensure the robust End-to-End production of our new mRNA Individualized Neoantigen Therapies (INT). The individual will work collaboratively with cross functional stakeholders such as Technical Development, Manufacturing, Regulatory, and Quality, to ensure all technical aspects of production are successfully executed. This will be a 3rd shift role, working a Wednesday through Saturday schedule from 10:00pm until 8:00am. | 2/16/2024 |
| 3253 | Moderna Therapeutics Norwood, MA Engineer II, MST - PCV Biochemical engineer, Chemical engineer, Biochemistry or Biology background. MS. Exp: 1 to 3 years’ |
The Specialist, MS&T will be part of Moderna’s Manufacturing Science and Technology team responsible for process implementation, technical support, and person-in-plant coverage to ensure the robust End-to-End production of our new mRNA Personalized Cancer Vaccine (PCV). The individual will work collaboratively with cross functional stakeholders such as Technical Development, Manufacturing, Regulatory, and Quality, to ensure all technical aspects of production are successfully executed. This will be a 1st shift role and the individual will be working a Wednesday through Saturday schedule from 6:00am until 4:00pm. | 2/16/2024 |
| 3254 | Nanostring Bothell, WA Manufacturing Assembly Technician I 2-year degree in a Life Science related discipline (Chemistry, Molecular Biology, Biotechnology, etc.) Exp: 0+ years |
The Manufacturing Lab Technician is responsible for supporting the production of reagents used in various NanoString Analysis Systems, for example, nCounter® and GeoMx®. The role requires learning and performing both manual and automated production processes for the manufacturing of raw, intermediate, and final reagents needed for the multiplexed detection and the quantification of many different types of target molecules from biological samples. In this role, the Lab Tech will learn the skills to operate semi-automated and automated scientific equipment, perform Standard Operating Procedures (SOPs), navigate Document Control systems, Enterprise Resource Planning (ERP) systems, etc. | 2/16/2024 |
| 3255 | Nanosyn Mississauga, Ontario Canada, CA Chemist I (Trace Metals) B.Sc. in chemistry or related field. Exp: 1 -2 years’ |
Under the supervision of the Supervisor, Trace Metals and Manager, Trace Metals and GMP Testing, this position is responsible for the following: Perform routine chemical and physical analysis on the full range of analytical samples in accordance with in-house methods, customer’s method or compendial method primarily using Inductively Coupled Plasma Mass Spectrometry (ICP-MS)/ Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES)/ Atomic Absorption Spectroscopy (AAS) Perform and maintain Trace Metals instruments- performance verifications, troubleshoot when required Assists with method development, method validation testing and analytical method transfer testing using ICP-OES/ ICP-MS/ and AAS Prepare analytical reports, method validation protocols and reports for validations and verifications performed Maintain documentation, including lab notebooks, equipment logbooks and instrument raw data in accordance with applicable SOPs Inform and discuss with Manager any atypical / OOS result and deviations Perform pipette calibrations, washing of glassware, disposal of samples in accordance with in-house SOPs Assist Supervisor and Manager with other laboratory duties as required | 2/16/2024 |
| 3256 | Nanosyn Acton, MA Microbiologist I (Entry Level) Graduation in microbiology / equivalent. Exp: 1-2 year |
Element has an opportunity for a Microbiologist I whose primary responsibility is to support laboratory operations by conducting the relevant microbiological testing. | 2/16/2024 |
| 3257 | Nanosyn Midland, MI Chemist Bachelors. Exp: 0-2 years’ |
Element has a current opening for a Chemist to join our growing team in Midland, MI. The Chemist executes analytical methods and perform testing using a variety of technologies, under the supervision of more senior staff members and supervisor. | 2/16/2024 |
| 3258 | New England Biolabs Ipswich, MA Research Technician B.A or B.S. in Biology, Molecular Biology or related field. Exp: 1+ years |
The Sequencing Core at New England Biolabs Inc. (NEB) is seeking a Research Technician to support Next-Generation sequencing (NGS) and DNA analysis operations of the group. As a member of the Sequencing Core, this individual will interface with scientists across the Research, Product Development, and Production departments to deliver high-quality data. | 2/16/2024 |
| 3259 | NorthEast BioLab Hamden, CT Associate Scientist, Central Laboratory Services B.S. in Physiological Science, Epidemiology, Microbiology, Immunology, Genetics, Biology, Molecular Biology, Cell Biology, Biotechnology, Biochemistry Exp: Entry Level |
NOTE: PLEASE SUBMIT BOTH RESUME AND COVER LETTER TO APPLY FOR THIS JOB. KINDLY DISCUSS YOUR MOTIVATION, RELEVANT EXPERIENCE, SALARY REQUIREMENTS, AND VISA STATUS IN YOUR SUBMISSION. Role Gain an overall understanding of drug development and maintenance of the full chain of sample custody for regulatory compliance Support implementation of Laboratory Information management System (Watson LIMS) for sample management and storage Sample management and reconciliation, kit preparation and verification, and document preparation related to biological sample collection, storage, and shipment for clinical trials Streamline inventory management, consumable ordering, and other documentation requests for Quality Assurance Unit Help maintain ultra-low temperature (ULT) freezers and refrigerators and associated electronic logs and records Learn bioanalytical techniques for the analysis of drug and biomarkers in biological matrices Follow appropriate safety and study requirements by reading, understanding, and following Standard Operating Procedures (SOP), Good Laboratory Practices (GLP) requirements, and Sponsor Study protocols Support business development and marketing activities, foster client relationships, and help onboard new sponsors | 2/16/2024 |
| 3260 | Nelson Laboratories Taylorsville, UT Lab Analyst - Routine Chemistry (Day Shift, Mon-Fri) Bachelors Degree is relevant Life Science preferred. Exp: No Experience |
Laboratory Analysts conduct testing under supervised conditions in accordance with established procedures. Successful lab analysts are people who enjoy conducting tests following written instructions, who pay close attention to detail to make sure everything is done correctly, and who have high standards of personal integrity so that they deliver high-quality results. | 2/16/2024 |
| 3261 | Nephron Pharmaceuticals West Columbia, SC Quality Assurance Associate High School diploma with Bachelor of Arts or Science degree preferred. Exp: 1 year |
Manages the sampling, inspection, and release of production components, raw materials, as well as related corresponding documentation for use in manufacturing operations. Serves as primary reviewer for DHR documents and product release. Quality assurance process improvements. Coordinate incoming inspection equipment usage and maintenance. Assists with additional work duties or responsibilities as evident or required. Performs other duties as assigned or apparent. | 2/16/2024 |
| 3262 | Nephron Pharmaceuticals West Columbia, SC Microbiology Environmental Monitoring Technician - (Days & Nights Available) Associates of Science minimum; Bachelor’s degree with a science background preferred. Exp: 1+ years |
The Microbiology Environmental Monitoring (EM) Technician I is an entry level position that performs monitoring of air quality, environmental, and personnel throughout the facility. EM Technician I collects samples of water for injection (WFI) and performs enumeration. EM Technician I assists EM Leads, Supervisors, and Management with additional responsibilities as delegated. EM Technician I must uphold cGMP and Nephron’s core beliefs. | 2/16/2024 |
| 3263 | Nephron Pharmaceuticals West Columbia, SC Nitrile-QA Incoming Inspector Bachelor’s degree preferred. Exp: 1 year |
Receives, samples, inspects, and releases raw material chemicals within Nephron Nitrile’s electronic inventory system and process corresponding documentation necessary in manufacturing operations. Samples, inspects, and releases production components within Nephron Nitrile’s electronic inventory system. Ensures correct paperwork was obtained by warehouse personnel. Work with other departments to ensure receipts, sampling, and releases are within compliance and completed in a timely manner. Assists and performs additional work duties or responsibilities as evident or required. | 2/16/2024 |
| 3264 | Nephron Pharmaceuticals West Columbia, SC Microbiology Gowning Certification Coordinator Bachelor’s degree with a science background preferred. Exp: 1+ years |
The Microbiology Gowning Certification Coordinator is an expert on gown certification. Microbiology Gowning Certification Coordinator will lead all gown certification training and plating, as well as follow up with any re-training or re-certification necessary. Microbiology Gowning Certification Coordinator will maintain the certification schedule. When EM Trainer is unavailable, Microbiology Gowning Certification Coordinator will train EM Technician I and EM Technician II. Microbiology Gowning Certification Coordinator must uphold cGMP and Nephron’s core beliefs. | 2/16/2024 |
| 3265 | Neurocrine Biosciences San Diego, CA Associate Scientist, Analytical Chem Research Bachelor's degree in Chemistry, Biochemistry or similar discipline. Exp: 1+ years |
Assists medicinal chemistry efforts in purifying and analyzing small molecules by LC-MS and SFC. Supports a range of activities, including design, operation, and maintenance of all analytical instrumentation, including HPLCs, SFCs, mass spectrometers, liquid handlers, and solvent evaporators. | 2/16/2024 |
| 3266 | Nexcelom Bioscience San Diego, CA Research Associate I - Diagnostics Bachelor’s degree in a Life Sciences-related field. Exp: 1 years |
BioLegend (a division of Revvity, Inc.) is seeking a highly motivated Product Development Research Associate to join our Diagnostic Product Development Team. This position will actively participate in the development of flow cytometry reagents for diagnostic use. The responsibilities include: perform experiments, analyze and report results, troubleshoot, manage and maintain documentation. After three months in this role, you should be able to work independently to perform flow cytometry experiments, analyze data and document report. | 2/16/2024 |
| 3267 | Nexcelom Bioscience San Diego, CA Research Associate I - Antibody Development Bachelor of Science or equivalent degree with coursework in cell biology, immunology, and biochemistry. Exp: 1+ years |
This person would be responsible for developing monoclonal (or polyclonal) antibodies in BioLegend derived from immunized animals by performing antigen preparation, host immunization, bleed analysis, cell fusion, and small-scale antibody purification. Techniques involved in this job include antigen formulation, animal immunization and tissue harvesting, cell culture, cell fusion, and antibody analysis using ELISA, WB, and other techniques. | 2/16/2024 |
| 3268 | Lifecore Biomedical Chaska, MN Associate Manufacturing Engineer - Automation BS in Engineering or Automation Engineering Technology Degree. Exp: entry level |
This full-time position offers incredible benefits, your choice of a 2nd shift - 4 day work week or a weekend shift - 3 day work week, and a company culture focused on development and growth which include promotion opportunities. In this entry level engineering role you'll have the opportunity to utilize and enhance your skills in a highly regulated industry by supporting automated manufacturing processes by designing and implementing improvements and troubleshooting and resolving issues. | 2/5/2024 |
| 3269 | Lifecore Biomedical Chaska, MN QC Lab Coordinator I Bachelor’s Degree in life science or equivalent combination of education and experience. Exp: 1-3 years |
This full time position offers incredible benefits, your choice of a 4 ½ or 5 day work week, and a company culture focused on development and growth which include promotion opportunities. As the QC Lab Coordinator, you will support the Quality Control department in meeting their goals and accountabilities by trending department data and reporting key metrics. You will manage scheduling and coordinate with other departments to ensure timelines are maintained. You will also perform LIMS and ERP transactions, coordinate with external vendors, and assist with creating, updating, and reviewing supporting QC documentation. | 2/5/2024 |
| 3270 | Lonza Durham, NC Cell Culture Technician AA degree Exp: 1-3 years |
Lonza Durham has an exciting opportunity for a Cell Culture Technician to perform tissue culture, tissue isolations and media production with a high degree of aseptic and technical skill. The Cell Culture Technician facilitates departmental function including training lower-level technicians, laboratory maintenance and cleaning, assisting with planning and ordering, writing protocols, performing and reporting on experiments, upholding departmental standards, and reviewing batch records. The Cell Culture Technician is responsible for the manufacture and assembly of products used in clinical research including operation of production equipment, maintaining records, and laboratory environment to comply with Good Manufacturing Practices (GMP), ISO 9000 regulations, and Standard Operating Procedures. The Cell Culture Technician may assist with in process testing to assure batches meet specifications. The training schedule, following orientation, will be Monday – Friday, 8am – 5pm for up to 12 weeks. After training, the work schedule will be Tuesday - Saturday, 8am – 5pm. Occasional evening and weekend work required | 2/5/2024 |
| 3271 | Lonza Portsmouth, NH Manufacturing Project Associate 2 (Biologics Manufacturing) A.S. or B.S. degree preferred, with a focus in Biotechnology, Biology, Chemistry, or related STEM discipline. Exp: 1+ years |
The Manufacturing Project Associate Level II is an intermediate level position for an individual with technical manufacturing knowledge and preferably prior proven projects experience. As a level II, the individual is responsible for medium to large sized suite and process specific projects and projects that span across suites and/or the entire Manufacturing organization. The individual is responsible for owning and driving manufacturing improvement projects from concept to completion, with a particular focus on creating efficiencies that contribute to quality, cost, on-time delivery and right first time. The Project Associate supports by working cross-functionally and in collaboration with internal support departments, vendors, and Manufacturing suites to implement new systems, technology and/or procedures, update/create associated documentations and provide essential trainings. The individual will be expected to manage a number of projects at various stages of completion; managing priorities and ensuring on time and quality delivery of all assigned projects. In this level, individuals may become introduced to more customer and campaign focused responsibilities, including IPT/JPT and pre-campaign initiatives. | 2/5/2024 |
| 3272 | Lonza Portsmouth, NH Manufacturing Project Specialist (Biologics Manufacturing) A.S. or B.S. degree highly preferred, with a focus in Biotechnology, Biology, Chemistry, or related STEM discipline. Exp: 1+ years |
The Manufacturing Project Specialist works closely with Manufacturing Management to support the achievement of department goals, interdepartmental readiness and batch release requirements, and maintain due dates to support the on time release of batches. The Project Specialist supports by working cross-functionally and in collaboration with internal support departments, customers and Manufacturing suites to develop or update procedures or steps, identify and escalate risks, communicate changes and plan for execution. The Project Specialist is responsible for owning and driving manufacturing improvement projects from concept to completion, with a particular focus on creating efficiencies that contribute to quality, cost, on-time delivery and right first time performance. This role falls under Lonza's Hybrid Work Policy, which requires 3 days a week onsite. | 2/5/2024 |
| 3273 | Lonza Portsmouth, NH Biotechnologist Level 1 (A Shift Days) AS/BS preferred; Science related discipline. Exp: 1+ years |
Shift Schedule: The shift schedule is from 7am-7pm, on a rotational schedule every other week: Week 1: M/T/F/SAT/SUN Week 2: W/TH Shift differentials are included for weekends worked Initial 2 week training period on day shift Monday-Friday upon hire for new hires The Biotechnologist/Manufacturing Associate I is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP) conditions. Level I associates are expected to execute process recipes, follow written Standard Operating Procedures (SOPs), monitor equipment and processes, independently perform laboratory tasks, including pH, conductivity testing, product sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to demonstrate a strong understanding of cGMP compliance while operating under supervision, and aseptic technique in handling of products and materials. Level II Operators may also be asked to troubleshoot equipment events, initiate deviations, review batch records and logbooks | 2/5/2024 |
| 3274 | Lonza Portsmouth, NH Biotechnologist Level 2 (Upstream) - A Shift Days AS/BS preferred in relevant STEM field. Exp: 1+ years |
Shift Schedule: The shift schedule is from 7am-7pm, on a rotational schedule every other week: Week 1: M/T/F/SAT/SUN Week 2: W/TH The Biotechnologist Level 2 is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP) conditions. Level II associates are expected to execute process recipes, follow written Standard Operating Procedures (SOPs), monitor equipment and processes, independently perform laboratory tasks, including pH, conductivity testing, product sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to demonstrate a strong understanding of cGMP compliance while operating under supervision, and aseptic technique in handling of products and materials. Level II Operators may also be asked to troubleshoot equipment events, initiate deviations, review batch records and logbooks. | 2/5/2024 |
| 3275 | Lonza Portsmouth, NH Biotechnologist Level 1 (B-Nights) - Biotech Manufacturing AS/BS preferred; Science related discipline. Exp: 1+ years |
Shift Schedule: The shift schedule is from 7pm-7am, on a rotational schedule every other week: Week 1: M/T/F/SAT/SUN Week 2: W/TH Shift differentials are included for night shift and for weekends worked Initial 2 week training period on day shift Monday-Friday upon hire for new hires The Biotechnologist/Manufacturing Associate I is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP) conditions. Level I associates are expected to execute process recipes, follow written Standard Operating Procedures (SOPs), monitor equipment and processes, independently perform laboratory tasks, including pH, conductivity testing, product sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to demonstrate a strong understanding of cGMP compliance while operating under supervision, and aseptic technique in handling of products and materials. Level II Operators may also be asked to troubleshoot equipment events, initiate deviations, review batch records and logbooks. | 2/5/2024 |
| 3276 | Lonza Portsmouth, NH Biotechnologist Level 1 - Cell Therapy A.S., B.S., or vocational certificate in relevant STEM field is a plus. Exp: 1+ years |
Shift Schedule: The shift schedule is from 7am-7pm, on a rotational schedule every other week: Week 1: M/T/F/SAT/SUN Week 2: W/TH Shift differentials are included for weekends worked Initial 2 week training period on day shift Monday-Friday upon hire for new hires The Cell & Gene Therapy Biotechnologist/Manufacturing Associate will help to provide a safe, controlled work environment in all areas of expertise. Be aware of the site safety objectives and make sure they are communicated and understood. Biotechnologist/Manufacturing Associates will be proficient in an assigned area (i.e. Cell Growth, Drug Product Filling, etc.) and work in a team environment during manufacturing operations (i.e. harvest, fill/finish, visual inspection, etc.). | 2/5/2024 |
| 3277 | Loop Genomics San Diego, CA Research Associate, Surface Chemistry Bachelor’s degree in chemistry, materials science, biochemistry, bioengineering, physics, or similar fields. Exp: 0-2 years |
We are seeking a Research Associate, who has a curious mind and a great desire to learn new techniques in new areas of study to join our interdisciplinary research team. You will be learning experiment design pertaining to surface coating characterization assays, explore optimal surface coating process and support custom surface production needs. The preferred candidate will have scientific research lab experience, demonstrated by any combination of prior curricular, extracurricular undergraduate research lab work, scientific paper, poster, or presentations. | 2/5/2024 |
| 3278 | LSI Solutions Victor, NY Manufacturing Engineer - 8:00AM to 5:00PM Level I: BS Engineering or Engineering Technology; or Level II: MS. Exp: Level I: 0-2 years; Level II: 1 to 5 years |
The Manufacturing Engineer is responsible for developing and improving manufacturing processes. They design and refine production equipment and processes to improve capability, enhance productivity, reduce waste, reduce risk, and elevate overall product quality. Manufacturing Engineers introduce new technologies, perform root cause analysis, implement corrective actions, and leverage problem solving skills and equipment expertise to support ongoing production. | 2/5/2024 |
| 3279 | Lumen Bioscience Seattle, WA Lab Technician, Physiology BA/BS degree in molecular biology, microbiology, biochemistry, chemistry, biotechnology, biochemical engineering, or related field of study Exp: 1-3 years |
Lumen is seeking a highly motivated, innovative Lab Technician to join our team. The Laboratory Technician will support scientists in the Physiology research and development group. The work will involve several projects aimed at culturing Lumen’s spirulina-based platform organism. The individual will be focused on operating bioreactors under various run conditions and analyzing samples. The candidate is also expected to independently perform and learn new laboratory techniques, use specialized laboratory instruments, perform delicate manual procedures, follow and apply standard laboratory protocols and provide reliable, independent, and versatile support to biotechnology research. The position requires strong organizational skills and meticulous laboratory record keeping. Effective communication skills are crucial in coordinating with Lumen’s research and production scientists, in providing status updates, and in raising quality or troubleshooting issues as they may arise. | 2/5/2024 |
| 3280 | Lumen Bioscience Seattle, WA Lab Technician, Clinical B.S. in immunology, biochemistry, cell biology, microbiology, or related field of study. Exp: one year |
Lumen Bioscience Clinical Program Management is seeking a laboratory technician with clinical research laboratory experience. Working with scientists, the technician will support assay development efforts across multiple active clinical projects. The position also involves coordinating assay development internally with Lumen’s research, manufacturing, and quality teams. The technician will support equipment and supply requisition and inventory. In addition, the technician will maintain the clinical specimen archive. The position requires strong communication skills and an empathic understanding of where others are experiencing issues. Efficient problem-solving are crucial to keep pace with our growing company. Personal initiative and organizational skills will drive your career growth. | 2/5/2024 |
| 3281 | Luminex Madison, WI Design Assurance Engineer Bachelor's Degree Bachelor degree required, in a life science/engineering discipline required. Exp: 1+ Years |
The Design Assurance Engineer acts as the quality representative on design core teams for electromechanical instruments, reagents and assays for the life science and in-vitro diagnostics market. Design Assurance Engineer is responsible for guiding the development teams through the Design Control process ensuring compliance with FDA, ISO, QSR, quality, safety and environmental regulations and internal procedures. The Design Assurance Engineer may also provide support for quality initiatives, post market design changes/improvements and quality surveillance activities. | 2/5/2024 |
| 3282 | Luminex Northbrook, IL Manufacturing Associate I, Microarray Associate's Degree in Chemistry, Life Sciences, Biotechnology, or Medical Technology related fields required. Exp: 1+ Years |
Delivering manufacturing requirements against production schedule within a focused manufacturing operation and/or product segment. Work schedule may include alternate shifts. Following approved cGMP manufacturing instructions and personnel are required to complete a history record of the lot built per company Quality System. | 2/5/2024 |
| 3283 | Luminex Cypress, CA Cell Culture Technician II Requires Bachelor’s Degree in Biology or related field or equivalent experience. Exp: 1+ Years |
Responsible for manufacturing and assembly of clinical and commercial products. Operates production equipment. Weighs, measures and checks raw materials to assure batches manufactured contain proper ingredients and quantities. Performs Cell Culture activities using aseptic technique. Maintains records and laboratory environment to comply with regulatory requirements, Good Manufacturing Practices and Standard Operating Procedures. Assist with in-process testing to assure batches meet specifications. Assignments are moderately complex in nature where judgment is required in resolving problems and making routine recommendations. Supports all applicable regulations including but not limited to FDA, ISO, and CMD/CAS requirements. | 2/5/2024 |
| 3284 | Luminex Stillwater, MN Process Scientist I Bachelor's or Master's degree in Chemistry, Biology, Medical Technology or related science field. Exp: 1+ years |
This position is responsible for material processing, reagent formulation, technical manufacturing, in-process and final quality control of reagents, components and in-vitro diagnostic products. | 2/5/2024 |
| 3285 | Luminex Stillwater, MN Engineering Technician BS in Engineering Exp: 1-2 years |
As an Equipment Technician, you will be an administrator and expert of the equipment used in the manufacture of in vitro diagnostic products. In addition, you will drive operational improvement activities that involve equipment procurement, validation, or the transfer of information from equipment. This is a fast-paced, deadline-driven department that provides centralized support to the organization. Be a Subject Matter Experts (SME) for equipment and equipment validations to implement changes to business systems and processes, interacting and working collaboratively with teams across Diasorin. | 2/5/2024 |
| 3286 | Horizon Therapeutics Thousand Oaks, CA Engineer Master’s degree in Engineering Exp: 0 - 2 years |
Let’s do this! Let’s change the world! In this dynamic role you will serve as the system owner for process equipment in a state of the art bulk biopharmaceutical manufacturing facility. | 2/7/2024 |
| 3287 | Horizon Therapeutics Holly Springs, NC Engineer - Plant Utilities Master’s Degree in Chemical or Mechanical Engineering Exp: 0 - 2 years |
Let’s do this! Let’s change the world! The Engineer System Owner will be joining the Facilities & Engineering (F&E) group to partner closely with the corporate engineering team to design, build, commission, and qualify new equipment and systems needed for drug substance production, as well as developing subject matter expertise to support operations upon start up. | 2/7/2024 |
| 3288 | HRA Pharma Covington, OH Microbiologist I - Nights A four-year college degree in Microbiology or Biological Science. Exp: One years |
Perrigo Nutritionals, located in Covington, OH is looking to add a Night shift Microbiologist to their team. The hours for this position are, 6pm - 6am working a rotating 2/2/3 schedule Scope of the Role The successful candidate will be able to work in a safe and efficient manner in accordance with current GLP’s, SOP’s, analytical methods, and work instructions. Excellent communication skills, attention to detail, and the ability to work both independently and as part of a team are desired. A thorough understanding of aseptic technique is essential. Microbiological testing is performed on raw materials, in-process samples, finished products, water samples, and environmental swab samples. | 2/7/2024 |
| 3289 | HRA Pharma Georgia, VT Chemistry Analyst I - 2nd Four-year college degree in chemistry or related science. Exp: 1-2 years |
The incumbent performs a variety of standard analyses on raw material, in-process, and finished product samples using chemical analysis techniques, according to compendia (i.e. USP, FCC, or AOAC) or Perrigo methodologies. Performs routine analyses of raw material and finished product samples as assigned, demonstrates proficiency in 5 – 10 separate Analytical Methods (AM’s). Analytical instrumentation used in this group is primarily NMR Fat Analyzer, Nitrogen Analyzer, NIR Spectroscopy, and HPLC (High Pressure Liquid Chromatography). | 2/7/2024 |
| 3290 | ICU Medical Austin, TX Chemistry Analyst I - Night Shift - (24300022) Bachelor’s Degree is required: Chemistry, Chemical Engineering, or Chemical Science. Exp: 0-2 year |
The Chemistry Analyst I will work under direct supervision or be partnered with an experienced analyst to perform wet chemistry analyses, preparation of reagents, standardization of solutions, and instrumentation testing and documentation in a cGMP environment. May be cross-trained to work in other laboratory areas as dictated by the needs of the department. | 2/7/2024 |
| 3291 | Integrated DNA Technologies Coralville, IA Technician II Associate’s (2 year) degree. Bachelor’s (4 year) degree preferred. Science related field preferred. Exp: 1+ years |
This position is part of the Production department located in Coralville, IA and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things. Shift: Sunday – Thursday 3:00PM – Midnight | 2/7/2024 |
| 3292 | Integrated DNA Technologies Coralville, IA Job Posting Title Technician II (Synthesis -Long Oligo) Associate or bachelor’s degree in a Science related field preferred. Exp: 12 months |
This position is part Shipping, Receiving and Distribution department of the located in Coralville, IA and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things. Shift: Monday-Thursday 9:00pm-7:30am | 2/7/2024 |
| 3293 | Integrated DNA Technologies Coralville, IA Technician II (Synthesis - MNP) Associate or bachelor’s degree in a Science related field preferred. Exp: 12 months |
This position is part Shipping, Receiving and Distribution department of the located in Coralville, IA and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things. Shift: Wednesday -Friday 7PM-7AM. | 2/7/2024 |
| 3294 | Integrated DNA Technologies Coralville, IA Technician II, Stock Product Associate’s (2 year) degree or comparable combination of education and experience required. Bachelor’s (4 year) degree preferred. Science related fi Exp: 1+ years |
This position is part of the Production department located in Coralville, IA and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things. Shift: Sunday – Thursday 3:00PM – Midnight | 2/7/2024 |
| 3295 | Integrated DNA Technologies Coralville, IA Technician II (Formulation - GMP) - Overnight Associate’s (2 year) degree or comparable combination of education and experience required. Bachelor’s (4 year) degree preferred. Science related fi Exp: 1+ years |
This position is part of the Production department located in Coralville, IA and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things. Shift: Weekday Overnight; Monday – Thursday 8:30pm-7:00am | 2/7/2024 |
| 3296 | Illumina San Diego, CA Scientist 1: Assay Product Development BS/MS in Biochemistry, Molecular Biology, Chemistry, Biology, Bioengineering, or related disciplines. Exp: 1-2 years |
We are looking for a contract Scientist 1 to join the assay development team within Illumina Product Development. This person will be contributing to new technologies and workflows for Illumina customers as part of a collaborative team. This is a hands-on position where you will primarily be responsible for the design, execution, and analysis of experiments to support assay development and optimization. | 2/7/2024 |
| 3297 | Lyophilization Services of New England Bedford, NH QA Associate I - Operations Bachelor’s Degree in a relevant scientific discipline preferred. Exp: 0-2 years |
The Quality Associate I - Operations is responsible to provide QA support real-time for GMP Manufacturing of drug product. Responsibilities include providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. Real time continuous monitoring of manufacturing related systems and processes to ensure compliance with applicable regulatory and industry standards, needed quality improvements, and safety/efficacy for phase appropriate GMP manufacture of drug products. | 2/8/2024 |
| 3298 | Lyophilization Services of New England Madison, WI QC Chemist I Bachelor of Science in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study. Exp: 0-3 years |
The QC Chemist I will have responsibility to support various activities in the Quality Control Laboratory. This includes testing the following sample types R&D, in-process, finished product, stability, as well as raw materials. Job duties may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management | 2/8/2024 |
| 3299 | Lyophilization Services of New England Bedford, NH QA Associate I - Operations Bachelor’s Degree in a relevant scientific discipline preferred. Exp: 0-2 years |
The Quality Associate I - Operations is responsible to provide QA support real-time for GMP Manufacturing of drug product. Responsibilities include providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. Real time continuous monitoring of manufacturing related systems and processes to ensure compliance with applicable regulatory and industry standards, needed quality improvements, and safety/efficacy for phase appropriate GMP manufacture of drug products. | 2/8/2024 |
| 3300 | Maverick Therapeutics Social Circle, GA Manufacturing Technician II AA or higher. Exp: 1+ years |
As a Manufacturing Tech II, you will execute all processes in production while strictly following cGMP, environmental health and safety guidelines and any other related regulations which could apply. In addition to making routine revisions to documents, you may rewrite complex procedures or initiate new procedures as applicable. You will have enough applied technical knowledge to perform complex trouble shooting tasks and may even assist during the transfer of new technologies into manufacturing. You will have technical and administrative competence to organize and lead production activities, including demonstrating leadership in cGMP compliance, and environmental health and safety skills. You will report to Manufacturing Supervisor. | 2/9/2024 |
| 3301 | Maverick Therapeutics Thousand Oaks, CA Manufacturing Associate - Day Bachelor's degree preferred. Exp: 0-2 years |
Under the general direction of the Manufacturing Lead and overall direction of the Supervisor, the Manufacturing Associate executes all processes in the production area while strictly adhering to CGMP, environmental health and safety guidelines and any other related regulations. | 2/9/2024 |
| 3302 | Maverick Therapeutics Round Lake Beach, IL Manufacturing Technician II AA or higher. Exp: 1+ years |
As a Manufacturing Technician II, you will implement all processes in production while strictly following cGMP, environmental health and safety guidelines and any applicable related regulations. You will have technical and administrative competence to organize and lead production activities. You will participate in both departmental projects and any quality working teams which may be applicable. Responsibilities include assisting with the movement of Flexbumin between the different stages of inspection to packaging within the value stream. You may act as line lead, and will ensure the line operates smoothly and keeps up with daily goals. You will also document your process activities on routers or in the electronic batch management system (EBM). You will report to the Supervisor, Manufacturing. | 2/9/2024 |
| 3303 | Maverick Therapeutics Thousand Oaks, CA Manufacturing Associate - Night Shift Bachelor's degree preferred. Exp: 0-2 years |
Under the general direction of the Manufacturing Lead and overall direction of the Supervisor, the Manufacturing Associate executes all processes in the production area while strictly adhering to CGMP, environmental health and safety guidelines and any other related regulations. This position is a night shift role. | 2/9/2024 |
| 3304 | Medtronic Cherry Hill, MA Microbiologist II Bachelors degree required. Exp: one year |
Responsibilities may include the following and other duties may be assigned. Interacts with Purchasing and Contract Sterilization/Test Facilities to ensure that the Sterilization requirements and product testing procedures are clear, complete and understood. Works with the internal personnel as well as with the Contract Sterilization and Test facilities to establish specifications and coordinates the new product sterilization validations as well as the quarterly validations. Work with different Subject Matter Expert to evaluate changes impacting the product families, controlled rooms and critical systems. Coordinates yearly and quarterly product re-verifications (Irradiation & Ethylene Oxide)Coordinate lethality testing for EO product, or process qualifications Product Release (EO & Gamma) Develop and Coordinate Steam Sterilization Studies Develop and Coordinate Reusable Device Validation (Cleaning Studies) Develop and Coordinate Profiling Protocols | 2/9/2024 |
| 3305 | Medtronic Northridge, CA Biomedical Engineer II Masters of Science in Biomedical Engineering, Chemical Engineering, or related disciplines. Exp: 0+ years |
As a member of the Medtronic Diabetes – Continuous Glucose Monitoring Sensor R&D team this Product Development Engineer II will support the development of next generation CGM products. This position will play a key role in the early stage development of various new/improved chemistry layers/coatings of glucose sensors by designing and executing design optimization and characterization studies in preclinical & clinical studies. The role includes process development for feasibility clinical manufacturing. To this end, you will be responsible for driving the product build documentation, coordinating the fabrication & builds of prototype sensors for benchtop, preclinical and clinical evaluations, execute data trending & statistical process analysis. Upon successful proof-of-concept through feasibility studies, this role will subsequently support tech transfer to process & manufacturing teams. You will manage deliverables for multiple projects and maintain an effective system for tracking progress. You will be interfacing with Managers, Engineers &Technicians in R&D and New Product Introduction (NPI) Operations teams as well as Quality and Clinical groups to accomplish day to day activities. The candidate must have strong organizational skills, attention to details, an analytical mindset and ability to communicate effectively with multiple stakeholders. | 2/9/2024 |
| 3306 | Medtronic Bedford, MA Quality Engineer II Advanced degree in related engineering discipline required (Biomedical, mechanical, manufacturing, etc.). Exp: 0 years |
In this exciting role as a Quality Engineer II in the Bedford/Billerica facilities, you will have responsibility for supporting the quality and daily manufacturing of high-quality and complex catheters to support the Cardiac Ablation Solutions Business. In this role you will be part of a team that grows the operations capacity over 8X to support our customer needs in this newly acquired product portfolio. You will lead improvements in manufacturing quality, capacity, and stability through solving problems, developing solutions, and executing strategies. | 2/9/2024 |
| 3307 | Medtronic Billerica, MA Manufacturing Engineer II Advanced degree. Exp: 0 years |
Responsibilities may include the following and other duties may be assigned. Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling. Designs arrangement of machines within plant facilities to ensure most efficient and productive layout. Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance. Adapts machine or equipment design to factory and production conditions. May incorporate inspection and test requirements into the production plan. Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality. Develops manufacturing processes that are applicable to statistical process control, and may develop those techniques. Provides guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques. | 2/9/2024 |
| 3308 | Genentech Hillsboro, OR MANUFACTURING ASSET ENGINEER I/II, HTO B.S or higher in Mechanical Engineering, Electrical, Chemical, Biochemical, or related discipline. Exp: 0-2 years’ |
The Asset Engineer I/II is responsible for supporting the design, operation, control and optimization of manufacturing equipment at HTO. The position serves as the equipment owner and is engaged in development, qualification, data analysis, troubleshooting, and continuous improvement activities. The Asset Engineer plays a key role in day-to-day operations, as well as design and delivery of local and major capital projects, and interacts with a cross-functional team to deliver on business objectives. | 1/25/2024 |
| 3309 | Genentech Hillsboro, OR MANUFACTURING TECHNICIAN (CONTRACTOR) Graduate of a two-year Associates Degree program in Electrical/Mechanical Technology (or equivalent) is a plus. Exp: 1 to 2 years (within the last 7 years) |
Under the direction of the Process Unit Lead, perform a wide variety of tasks and operations that are required to formulate, fill, inspect and package sterile pharmaceutical products in a state-of-the-art, automated production and packaging facility. Troubleshoot, maintain, assemble, install, and repair all electronic, mechanical, and instrumentation devices on production equipment as required. Assist on major equipment overhauls, repairs, and installations as necessary. All operations carried out in compliance with cGMPs, Standard Operating Procedures (SOPs), product recipes, and Genentech standards. Duration: 6-month contract with possible extensions up to 3 years Day Shift, 6:00 am – 6:30 pm, Sunday -Tuesday plus every other Wednesday Day Shift, 6:00 am – 6:30 pm, Thursday -Saturday plus every other Wednesday Day Shift, 5:30 am - 4:00 pm, Monday - Thursday Swing Shift, 12:00 pm -10:30 pm Monday - Thursday Night Shift, 6:00 pm -6:30 am, Sunday-Tuesday plus every other Saturday Night Shift, 6:00 pm – 6:30 am, Wednesday – Friday plus every other Saturday | 1/25/2024 |
| 3310 | Genentech Hillsboro, OR MANUFACTURING ASSET ENGINEER I, HTO (TWO YEAR TERM) B.S or higher in Mechanical Engineering, Electrical, Chemical, Biochemical, or related discipline. Exp: 1-2 years’ |
The Asset Engineer is responsible for supporting the design, operation, control and optimization of manufacturing equipment at HTO. The position serves as the equipment owner and is engaged in development, qualification, data analysis, troubleshooting, and continuous improvement activities. The Asset Engineer plays a key role in day-to-day operations, as well as design and delivery of local and major capital projects, and interacts with a cross-functional team to deliver on business objectives. | 1/25/2024 |
| 3311 | Genentech Vacaville, CA MANUFACTURING TECHNICIAN-BIOPROCESS (CONTRACTOR) Desirable but not required: AS/BS/BA in Biological Sciences, Physical Sciences. Exp: 1+ years |
As a Manufacturing Technician, you will be responsible for producing innovative bio-therapeutic medicine by interfacing with highly automated production systems and controls in a current Good Manufacturing Practices (cGMP) environment. You will maintain areas in a high state of inspection preparedness and will utilize business systems for inventory and process management. You will maintain records to comply with regulatory requirements utilizing cGMP and Standard Operating Procedures (SOPs) and will participate in the routine production of mammalian cell culture products within the Vacaville Manufacturing Facility, operating in at least one of the following production areas: Upstream Manufacturing (UM): Primary focus is the cleaning, sterilization and operation of fixed vessel systems for media preparation, fermentation, and harvest operations; perform seed train operations; perform dispensing of components; handle and aliquot hazardous materials. Downstream Manufacturing (DM): Responsibilities include the operation and cleaning of fixed tank systems, the operation and cleaning of filtration systems, large-scale buffer preparation, and the operation of column chromatography systems; perform dispensing of components; handle and aliquot hazardous materials | 1/25/2024 |
| 3312 | Genentech Oceanside, CA BIOPROCESS MANUFACTURING TECHNICIAN (CONTRACT) Preferred - Degree in Life Sciences/Engineering, Associate’s or Biotech certificate from approved program. Exp: 1+ years |
At Genentech, we are dedicated to pursuing groundbreaking science to discover and develop medicines for people with serious and life-threatening diseases. As a Bioprocess Manufacturing Technician, you will be responsible for producing medicine in a highly automated and controlled environment. Each product has a specific recipe; you will follow this recipe, along with the standard operating procedures, to operate the production equipment across various areas, including raw material dispensing/aliquoting, cell culture and purification. You will maintain records and follow all the steps necessary to comply with regulatory requirements within a current Good Manufacturing Practices (cGMP) environment. This is a contract role with the possibility of conversion to a permanent employee position. | 1/25/2024 |
| 3313 | Genentech Oceanside, CA ENGINEER I Bachelor's or Master's degree in Engineering or Life Sciences. Exp: 0-4 years |
Responsible for supporting operations in the Oceanside Pilot Plant and Process Engineering Purification/Analytical Lab. Deliverables include but are not limited to: HPLC-based analytics, rapid bioburden/endotoxin, lab scale and pilot scale chromatography, UFDF operations, buffer prep, column packing, equipment maintenance and preparation of technical reports. May commission new equipment, troubleshoot equipment and systems, develop new equipment requirements and operating parameters, and provide factory and site acceptance testing. Provide scientific and technical support to GMP Manufacturing Operations in a multi-product, large scale, automated biopharmaceutical facility. Support process validation through large and small-scale studies, protocol and report preparation, validation sampling, and sample shipments. | 1/25/2024 |
| 3314 | Grand River Aseptic Manufacturing Grand Rapids, MI QC Chemist I Bachelor’s degree in Chemistry and/or other related discipline (e.g. Biochemistry, Biotechnology). Exp: 1-3 years |
The Quality Control Chemist is responsible for supporting quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties will include, but are not limited to, providing general laboratory support for raw material, in-process, stability, and finished product testing. | 1/25/2024 |
| 3315 | Grand River Aseptic Manufacturing Grand Rapids, MI QC Lab Technician Bachelor’s degree in a related field (Biochemistry, Biotechnology, etc.). Exp: 0-2 years’ |
The QC Lab Technician supports quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties will include but are not limited to providing general laboratory support for sampling of raw material, incoming stability and finished product sample processing, basic physical testing, and inventory administration. | 1/25/2024 |
| 3316 | Grand River Aseptic Manufacturing Grand Rapids, MI Aseptic Manufacturing Associate (2nd and 3rd shifts) Bachelor’s degree, or equivalent experience. Exp: 0-1 year |
The Aseptic Manufacturing Associate (AMA) is responsible for performing various routine manufacturing tasks following established procedures and cGMP regulations under guidance of a production supervisor and/or senior management. | 1/25/2024 |
| 3317 | GreenLight Biosciences Rochester, NY Bioprocess Technician 4-year degree in Chemistry, Biochemistry, Biotechnology, Chemical Engineering. Exp: 1+ years |
GreenLight Biosciences is seeking a highly motivated Bioprocess Technician with education/experience in biotechnology, microbiology and biochemistry process operations at development scale. The successful candidate will become a member of the Rochester, NY pilot plant team and support their overall mission of delivering high performance RNA production processes and products to the market. Exact level dependent on qualifications including relevant experience. | 1/25/2024 |
| 3318 | Grifols Clayton, NC Utilities Project Engineer Bachelor's Degree in Engineering or related field. Exp: Engineer I: 0 years |
The Utilities Project Engineer will be responsible for the oversight of utilities projects for an industry leading biological therapeutic product manufacturer, Grifols as a member of the Facilities NA Project Engineering Team. The position will be stationed in Clayton, NC and will oversee Grifols projects on the east coast of the United States primarily, with the potential to oversee projects at other North American sites. Projects will include installation of clean and dirty utilities such as refrigeration systems, chillers, cooling towers, boilers, water purification systems, steam systems, waste systems, pumped distribution systems, and others, with some civil/structural oversight. Candidate should have a good understanding of the theory behind these types of systems as some system design and design reviews will be required. Candidate, through experience, should have knowledge of industry standards and best practices for utilities systems. Candidate must be willing to adjust working hours to meet the needs of the project(s), including some weekend work when required to match the schedule of project crafts. Some travel will be required - up to 25%. The position has the potential to progress into an engineering role / management role of increasing responsibility. | 1/25/2024 |
| 3319 | Grifols Vista, CA Manufacturing Technician Associates Degree or Bachelor’s degree preferred. Exp: 1-2 years’ |
Monday – Friday 6:30AM – 3:00PM The Manufacturing Technician I performs fundamental tasks within a GMP environment in support of more complex manufacturing operations. The Tasks include, but are not limited to, cleaning and maintaining the work place so that it meets the standards for controlling bioburden levels; cleaning operating equipment per applicable procedures so that it meets the standards established to prevent product contamination and maintaining records/logs neatly and accurately and in accordance with current standard procedures. The technician performs job tasks in a safe manner while following specific department safety rules. | 1/25/2024 |
| 3320 | Grifols Vista, CA Manufacturing Technician Associates Degree or Bachelor’s degree preferred. Exp: 1-2 years’ |
Monday – Friday 6:30AM – 3:00PM The Manufacturing Technician I performs fundamental tasks within a GMP environment in support of more complex manufacturing operations. The Tasks include, but are not limited to, cleaning and maintaining the work place so that it meets the standards for controlling bioburden levels; cleaning operating equipment per applicable procedures so that it meets the standards established to prevent product contamination and maintaining records/logs neatly and accurately and in accordance with current standard procedures. The technician performs job tasks in a safe manner while following specific department safety rules. | 1/25/2024 |
| 3321 | Grifols Los Angeles, CA QC Chemist Bachelor’s degree in Chemistry, Biochemistry, Biology or closely related scientific discipline is required. Exp: 1+ years |
The QC Chemist is responsible for performing routine and non-routine chemical and biochemical assays on protein-based therapeutics and raw materials. | 1/25/2024 |
| 3322 | Grifols Clayton, NC Quality Control Assistant/Associate Materials Eval. Coord. Associates degree with an emphasis in sciences or mathematics. Exp: one year |
Location: Clayton NC Shift: M-F 8am - 4:30pm The Quality Control Assistant/Associate Materials Evaluation Coordinator evaluates critical quality attributes (visual, dimensional, functional), coordinates required chemical and/or biological testing, and executes approved usage decisions on all quality managed material used at the facility. These evaluations are performed on a wide variety of materials including, but not limited to, chemicals, labeling components, primary drug container components, process hoses, sterilizing filters, and other critical raw materials. This is done by verifying compliance to specifications and testing requirements and ensuring required documentation is complete and accurate thus minimizing the possibility that the safety and efficacy of final products manufactured and tested using these quality managed materials is compromised or adulterated. The Coordinators perform the last detailed review of these materials prior to release for use thus sound judgment is essential. The QC Assistant/Associate Materials Evaluation Coordinator inspects product final container reserve samples according to approved standard operating procedures. The QC Assistant/Associate Materials Evaluation Coordinator may perform in the warehouse as a Quality representative for sampling, auditing, and making Quality decisions. In this area, the QC Assistant/Associate Materials Evaluation Coordinator audits raw material batches using designated ANSI sampling plans. Decisions made by QC Coordinators have major compliance and monetary implications for Grifols | 1/25/2024 |
| 3323 | GRO Biosciences Cambridge, MA RA/Senior RA, Application Sciences BS degree. Exp: 1 year |
We’re seeking an RA or a Senior RA with synthetic chemistry, protein biochemistry, and/or glycobiology experience who’s interested in learning new things, “wearing many hats”, and having a large impact on the growth of an early-stage company. Major responsibilities include experimental design, experiment execution, data analysis, and collaborating across a matrixed research team. Ideal candidates are collegiate, transparent, data-driven, motivated by novel challenges, and will think critically yet creatively about the company’s strategies for therapeutic development. | 1/25/2024 |
| 3324 | GlaxoSmithKline Marietta, PA Process Equipment Engineer BS Degree in engineering. Exp: 1 or more years |
Are you looking for an engineering role that allows you to leverage your technical knowledge in a state-of-the-art manufacturing environment? If so, this Process Equipment Engineer role could be an ideal opportunity to explore. The Process Equipment Engineer supports primary (bulk) vaccine adjuvant manufacturing in a 24/7 production facility as part of an Engineering and Maintenance Team. The team is responsible for maintaining equipment in a state of readiness through routine preventive maintenance and upgrades to extend its useful life. The Process Equipment Engineer will also lead continuous improvement projects to achieve Safety, Quality and Commercial objectives. As system experts, Engineers are relied upon to lead technical investigation impacting manufacturing processes | 1/25/2024 |
| 3325 | GlaxoSmithKline King of Prussia, PA Automation Engineer BS/BA in engineering, life sciences, biology or equivalent technical discipline. Exp: 3+ months |
As an Automation Engineer, you will provide engineering and technical support for process controls and manufacturing execution systems in the Biopharmaceutical Operations facility. Evaluate and develop technology, plan and implement modifications, troubleshoot and support process controls and manufacturing execution systems | 1/25/2024 |
| 3326 | Gyroscope Therapeutics Morris Plains, NJ Associate Scientist (Hours: Wed - Sat 2:30pm - 1:00am) BA or MS in chemistry, biochemistry, microbiology, or other related science. Exp: 0 - 5 years |
Under general direction, perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay, and raw materials, as appropriate). | 1/26/2024 |
| 3327 | Gyroscope Therapeutics Morris Plains, NJ Associate Scientist (Hours: Wed - Sat 7am - 5:30pm) BA or MS in chemistry, biochemistry, microbiology, or other related science. Exp: 0 - 5 years |
Under general direction, perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay, and raw materials, as appropriate). | 1/26/2024 |
| 3328 | Gyroscope Therapeutics Morris Plains, NJ Associate Scientist (Hours: Sun - Wed 7am - 5:30pm) BA or MS in chemistry, biochemistry, microbiology, or other related science. Exp: 0 - 5 years |
Under general direction, perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay, and raw materials, as appropriate). | 1/26/2024 |
| 3329 | Gyroscope Therapeutics Morris Plains, NJ Associate Scientist (Hours: Sun - Wed 2:30pm - 1:00am) BA or MS in chemistry, biochemistry, microbiology, or other related science. Exp: 0 - 5 years |
Under general direction, perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay, and raw materials, as appropriate). | 1/26/2024 |
| 3330 | Gyroscope Therapeutics Morris Plains, NJ Cell Processing Specialist I (Tuesday-Saturday am shift) Associate’s degree or Bachelor’s degree in relevant Engineering or Scientific discipline. Exp: 0 - 1+ years |
The Cell Processing Specialist is responsible for cell washing operations and verifying cell processing intermediate processing days of patient derived clinical and commercial cellular immunotherapy products. Cell Processing Specialist I will also be responsible for the formulation and verification of all media lots. Due to the nature of the starting material (patient cells) this role requires high level of proficiency and ownership of the process and media formulation. | 1/26/2024 |
| 3331 | Gyroscope Therapeutics Durham, NC BioProcess Engineer I - Upstream (2-2-3 rotation day shift) Bachelor of Science Degree in Biology, Chemistry, Biotechnology or applicable field. Exp: Entry level |
The BioProcess Engineer I is responsible for assisting with organizing, running, and sustaining the manufacturing operations process at the plant/site. | 1/26/2024 |
| 3332 | Gyroscope Therapeutics Morris Plains, NJ Cell Processing Specialist I Sun-Thurs. PM shift) Associate’s degree or Bachelor’s degree in relevant Engineering or Scientific discipline. Exp: 1 - 1+ years |
The Cell Processing Specialist is responsible for cell washing operations and verifying cell processing intermediate processing days of patient derived clinical and commercial cellular immunotherapy products. Cell Processing Specialist I will also be responsible for the formulation and verification of all media lots. Due to the nature of the starting material (patient cells) this role requires high level of proficiency and ownership of the process and media formulation. | 1/26/2024 |
| 3333 | HelixBind Boxborough, MA Research Associate BS in a Physical or Life Sciences/Engineering discipline. Exp: 1+ years |
We are seeking a talented and motivated individual to join our R&D Team as a Research Associate. The position offers the exciting opportunity to grow along with the Company as it takes its initial product through to FDA clearance and market launch while it, in parallel, grows its pipeline of impactful syndromic diagnostic assays. This is a great time to join the team, with plenty of opportunities to grow and lead new projects. | 1/26/2024 |
| 3334 | Helmer Scientific Noblesville, IN Electromechanical Engineer I BS degree in Engineering or Engineering Technology. Exp: 0-5 years |
This role supports Helmer Scientific, part of Trane Technologies Life Sciences Portfolio. Helmer Scientific designs, integrates, manufactures, markets, and distributes specialized medical and laboratory equipment to clinical and life science customers in over 125 countries, as well as provide after-market service and support. Provides electromechanical engineering support to Engineering department through the development, documentation and production support for Helmer product development. Develop specs for mechanical and electrical engineering requirements based on directions given by Manager. Have fundamental knowledge from educational background, while tasks are managed or directed by others | 1/26/2024 |
| 3335 | Heska Mississauga, On Temporary-Laboratory Generalist 1 - (Overnight) Associates/Bachelor’s Degree in Science related field or Veterinary Technician. Exp: 1 year |
Receives and prepares samples for laboratory analysis and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. May perform a variety of client service activities for internal and external stakeholders. Shift: Monday - Friday 11pm - 7:30am Saturday on rotation | 1/26/2024 |
| 3336 | Heska West Palm, FL Stat Lab - Lab Generalist I Associates/Bachelor’s Degree in Science related field or Veterinary Technician. Exp: 1 year |
HOURS: The hours for this position are Monday - Friday from about 12:30pm - 6:30pm. PURPOSE OF JOB: Receives and prepares samples for laboratory analysis and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. May perform a variety of client service activities for internal and external stakeholders. | 1/26/2024 |
| 3337 | Heska Chantilly, VA Lab Generalist I (overnight) Associates/Bachelor’s Degree in Science related field or Veterinary Technician Exp: 1 year |
Receives and prepares samples for laboratory analysis and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. May perform a variety of client service activities for internal and external stakeholders. Shift: Monday - Friday 11:30pm - 8:00am Alternating Saturdays 10:00pm - 7:00am Includes night shift differential. ESSENTIAL DUTIES AND RESPONSIBILITIES: | 1/26/2024 |
| 3338 | Heska Irving, TX Lab Generalist I (Overnight) Associates/Bachelor’s Degree in Science related field or Veterinary Technician. Exp: 1 year |
Receives and prepares samples for laboratory analysis and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. May perform a variety of client service activities for internal and external stakeholders. | 1/26/2024 |
| 3339 | Heska Mississauga, O Microbiology Technician I(Day Shift)Temporary 4 year degree in Science-related field preferred. Exp: 6 months |
The Microbiology Laboratory Technician I performs laboratory analyses and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. Shift: Monday - Friday 9:00am - 5:30pm. Weekends would be on rotation. | 1/26/2024 |
| 3340 | Heska Oak Brook, IL Parasitology Technician 2, 3 or 4 year degree in Science-related field. Exp: 6 months |
The Parasitology Laboratory Technician performs laboratory analyses and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. | 1/26/2024 |
| 3341 | Heska Atlanta, GA Parasitology Technician - Day Shift 2, 3 or 4 year degree in Science-related field. Exp: 6 months |
The Parasitology Laboratory Technician performs laboratory analyses and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. SHIFT: Monday-Saturday 8am-430pm | 1/26/2024 |
| 3342 | Hikma Cherry Hill, NJ Chemical Process Operator I - 3rd Shift Associates Degree in Science or equivalent Exp: 1-year |
Using company procedures and guidelines, the Chemical Process Operator I is responsible for a limited spectrum of duties within the department. This may include weighing, mixing, equipment cleaning, tank cleaning, tank movement and PM activities, etc. This job has no supervisory responsibilities; however, the ability to assume higher level responsibilities and/or have demonstrated leadership abilities is preferred. | 1/26/2024 |
| 3343 | Hillrom Marion, NC Quality Lab Associate I - Bioburden (3rd Shift: M-Thu) B.S. degree in Microbiology, Biology, or related science. Exp: 0-2 years |
Conduct microbiological analysis on raw materials, solution, and components following approved Standard Operating Procedures in an accurate and timely manner. | 1/26/2024 |
| 3344 | Hillrom Plymouth, MN Engineer I - R&D Disposables (Hybrid) BS in Mechanical, Plastics, Biomedical Engineering or a related field, MS preferred. Exp: 0 - 1 year |
Document engineering concepts. Create, modify, and maintain design documentation per company procedures. Assist in the design and building of basic tooling, test fixtures and assembly equipment. Build prototypes and models and may operate machine tools. Understand customer needs through literature review, customer interviews, direct observation, competitive analysis, prototype evaluation, and clinical/simulated use studies. Write technical reports based on design verification analysis/testing for design changes and product design activities. Develop and execute test methods which specify measurement equipment, test set-up, measurement systems analysis, and data analysis. Identify, investigate, and solve engineering problems. | 1/26/2024 |
| 3345 | Hillrom Marion, NC Quality Associate l (2nd shift:3pm-11pm) Bachelor's degree strongly preferred. Degree in engineering or life science preferred. Exp: 1+ years |
Responsible for working with the manufacturing departments to address defects with the finished products. | 1/26/2024 |
| 3346 | Hillrom Marion, NC Quality Lab Associate I- Bioburden (5th Shift- 6AM to 6PM) B.S. degree in Microbiology, Biology, or related science. Exp: 0-2 years |
Conduct microbiological analysis on raw materials, solution, and components following approved Standard Operating Procedures in an accurate and timely manner. | 1/26/2024 |
| 3347 | Hillrom Saint Paul, MN Manufacturing Engineer I B.S. degree in Engineering or Science (Biomedical Engineer, Chemical Engineer, Mechanical Engineer, Electromechanical). Exp: 1+ years |
As a member of St. Paul's Engineering team, the Manufacturing Engineer supports daily initiatives from manufacturing teams to equipment to integrate new products within production goals (i.e., quality, delivery, cost, productivity, and safety). In this role you will support engineering improvement projects, participate in R&D activities, support key development and continuous engineering projects, drive KPI implementation and follow up. | 1/26/2024 |
| 3348 | Companion Medical Danvers, MA Microbiologist II Bachelors degree required. Exp: 1-2 years |
Responsibilities may include the following and other duties may be assigned. Interacts with Purchasing and Contract Sterilization/Test Facilities to ensure that the Sterilization requirements and product testing procedures are clear, complete and understood. Works with the internal personnel as well as with the Contract Sterilization and Test facilities to establish specifications and coordinates the new product sterilization validations as well as the quarterly validations. Work with different Subject Matter Expert to evaluate changes impacting the product families, controlled rooms and critical systems. Coordinates yearly and quarterly product re-verifications (Irradiation & Ethylene Oxide)Coordinate lethality testing for EO product, or process qualifications Product Release (EO & Gamma) Develop and Coordinate Steam Sterilization Studies Develop and Coordinate Reusable Device Validation (Cleaning Studies) Develop and Coordinate Profiling Protocols Develop Equipment Validations (steam, dry heat, incubators Documentation of all test procedures and validations Provide guidance to other non-exempt personnel within/outside the department | 1/18/2024 |
| 3349 | Companion Medical Bedford, MA Quality Engineer I Bachelors degree required. Exp: 0 years |
In this exciting role as a Quality Engineer I in the Bedford/Billerica facilities, you will have responsibility for supporting the quality and daily manufacturing of high-quality and complex catheters to support the Cardiac Ablation Solutions Business. In this role you will be part of a team that grows the operations capacity over 8X to support our customer needs in this newly acquired product portfolio. You will lead improvements in manufacturing quality, capacity, and stability through solving problems, developing solutions, and executing strategies. | 1/18/2024 |
| 3350 | Companion Medical Rice Creek, MN Quality Engineer I Bachelors degree required. Exp: 0 years |
In this exciting role, the Quality Engineer I will have responsibility for products built at Rice Creek Pharma Operations manufacturing site. Manufacturing Platform East employs the full breadth of our talent, technologies, products, services, and solutions to address the needs of customers and patients across the globe. The Manufacturing East Platform offers devices and therapies to treat abnormal heart rhythms, as well as cardiac diagnostic and monitoring solutions. Rice Creek Pharma Operations, or Fridley, offers devices within the defibrillation solutions, surgical infection control, and diabetes management portfolios. | 1/18/2024 |
| 3351 | Companion Medical Rice Creek, MN Software Engineer I Bachelors degree required. Exp: 0 years |
We are currently seeking a passionate Software Engineer I to join our Advanced Manufacturing Engineer (AME) Team. The Software Engineer I will support the design, development, and validation of Non-Product Software to support the automation and software integration operations for the development and commercialization of new combination devices (device/drug) | 1/18/2024 |
| 3352 | Companion Medical Plymouth, MN Manufacturing Engineer I Bachelors degree required. Exp: 0 years |
Engineers are indispensable to achieving our Mission. That’s why we empower you to bring the best of your experience to bear on our market-leading portfolio of innovations. Apply your existing skills and develop new ones, with the training, mentorship, and the guidance you need to continue to develop your expertise. Today, we’re partnering across the industry to confront systemic healthcare challenges – this requires bold leadership. If you want a challenging, energizing, rewarding career that changes lives, join us. We are currently hiring a Manufacturing Engineer I at our Plymouth, MN site. Make an impact on your community and the lives of others by leading sustaining efforts of cutting-edge medical devices. This Engineer would be responsible for first shift technical support of Cardiac Surgery product such as mechanical heart valves. Cardiac surgery represents end-state treatment in the care continuum for many cardiovascular diseases. There are approximately 1.8 million cardiac surgical procedures in the world on an annual basis. Cardiac surgery remains extremely important in treating complex disease and remains the gold standard on which many of the other therapies being developed in Cardiovascular are based upon. | 1/18/2024 |
| 3353 | Cook Biotech Winston Salem, NC Research and Development Engineer 2 Bachelor's degree in Engineering/Technology is required. Exp: 1-2 years |
The primary purpose of the Research and Development Engineer at Cook Winston-Salem is to design, test and technically document the feasibility, construction and production process of new and/or changed medical products. | 1/18/2024 |
| 3354 | Cook Biotech Winston Salem, NC Research and Development Engineer 1 Minimum four year degree in Engineering/Technology. Exp: 0+ years |
The primary purpose of this position is to design, test and technically document the feasibility, construction and production process of new and/or changed medical products. | 1/18/2024 |
| 3355 | Cook Biotech Bloomington, IN Manufacturing Engineer 1 Bachelor’s degree in Engineering or related field. Exp: 0 - 3+ years |
Responsible for providing technical support for the day-to-day production activities in the manufacture of custom, plastic components used in the assemblies of various medical devices. This is a hands-on position with visibility on the manufacturing floor and requires a high level of interaction with the production, product development, and quality teams. The engineer is responsible for supporting product development activities, continuous improvement, complaint resolution, CAPA investigations and other quality initiatives. | 1/19/2024 |
| 3356 | CordenPharma Boulder, CO QC Analyst - Nights Bachelor's Degree (BA) from 4-year college or university. Exp: 0 - 1 year |
Performs all technician tasks accurately and efficiently without supervision. Initiates expert technical advice to customers and completes all tasks in the Technician Training Manual. Maintains a high level of housekeeping and attention to detail. | 1/19/2024 |
| 3357 | Contract Pharmacal Hauppauge, NY Microbiologist; Quality Control Bachelor’s degree in a science related field. Exp: 1 - 9 years |
The Microbiologist is responsible for and has experience in performing microbial analysis for the QC Microbiology laboratory which is responsible for the analysis and disposition of commercial materials (raw materials, finished product release, stability, validation, investigation), and environmental samples, as assigned, and documenting results in accordance with SOPs. | 1/19/2024 |
| 3358 | Contract Pharmacal Hauppauge, NY Scientist I; Analytical R&D Bachelor’s or Master’s degree in chemistry or analytical chemistry. Exp: 1-2 years |
Design and conduct routine laboratory analysis using various analytical instruments and software such as HPLC, UPLC, ICP, and UV-Vis. | 1/19/2024 |
| 3359 | Contract Pharmacal Hauppauge, NY Lab Tech Associate degree. Exp: 1+ years |
The Laboratory Technician has primary responsibility for conducting basic routine lab analysis and maintaining all laboratory equipment, chemicals, and logbooks per CPC SOPs. | 1/19/2024 |
| 3360 | Crown Bioscience San Diego, CA Research Associate I - Biomarker & Diagnostic Tech Bachelor of Science degree or above in biotechnology, cell biology, immunology, oncology or other related disciplines. Exp: one year |
The purpose of the Research Associate I position is to provide support on biomarker discovery studies to meet company's goals, objectives and quality standards. | 1/19/2024 |
| 3361 | Crown Bioscience San Diego, CA Research Associate I - Cell Culture Technician Bachelor's degree in Biology, Biochemistry or related area. Exp: 1-2 years |
The purpose of the Research Associate I is to provide support with in vitro client studies and help with in vivo studies aligned with Company's goals, objectives and quality standards. | 1/19/2024 |
| 3362 | Cyprotex Framingham, MA Research Assistant BA/MS or equivalent experience in a relevant Biological or Chemical scientific discipline. Exp: 0-2 years |
The team is looking for a highly motivated Research Associate and/or Research Assistant that will be responsible for routine screening of compounds in various in vitro ADME/Tox assays and maintaining mammalian cells. Training opportunities will be provided for high throughput screening, mammalian cell culture and LC-MS/MS. Some cell culture and LC-MS experience are preferred. | 1/19/2024 |
| 3363 | Cyprotex Framingham, MA Research Associate BS/ MS in a relevant bio scientific discipline. Exp: 0-2 years |
The team is looking for a highly motivated Research Associate and/or Research Assistant that will be responsible for routine screening of compounds in various in vitro toxicology assays. | 1/19/2024 |
| 3364 | Cytovance Biologics Oklahoma City, OK AD Associate II MS in a life science field. Exp: 1+ years |
The AD Associate I/II position develops, optimizes, and qualifies analytical methods for biopharmaceutical products. The associate also supports drug development departments, such as Purification Department and Cell Culture Department, by performing analytical testing. | 1/19/2024 |
| 3365 | DiaCarta Richmond, CA Research Associate Sc. degree in molecular biology or a related field OR S. degree in molecular biology or a related field. Exp: Sc.: 0-1 years; S.: 0-2 years |
DiaCarta is seeking a highly motivated, independent, and interactive Research Associate to join the R&D function in the company. The new team member will participate in R&D activities with the goal of developing and launching new qPCR, NGS, and branched DNA tests for IVD cancer diagnostics applications. The successful candidate will have outstanding attention to detail, enjoy working in a fast-paced multidisciplinary team environment, and have exceptional hands-on laboratory skills. DiaCarta is a rapidly growing company, so the candidate must be highly motivated and committed to launching their career in an innovative area of molecular diagnostics. This is a full-time role in Richmond, and you will be reporting to the Senior Scientist. | 1/19/2024 |
| 3366 | DiscGenics Salt Lake City, UT Lab Calibration Technician Bachelors in Biological, Biochemical, or Chemistry related field. Exp: 1-2 years’ |
The Lab Calibration Technician is responsible for inspection, calibration, verification and maintenance of all laboratory equipment to meet established conformance standards. The Lab Calibration Technician will be responsible for performing routine maintenance according to the maintenance schedule or coordinating with external vendors or in-house experts to complete all tasks on time. The role may also be required to perform or coordinate non-routine repairs or calibration to ensure equipment is performing to internal standards. This role interacts with all levels of the organization in a collaborative and positive way with colleagues to facilitate department and organizational initiatives for cultural cohesion aligned to the DiscGenics Values. | 1/19/2024 |
| 3367 | Distributed Bio Seattle, WA Research Associate I B.S. in either animal science or similar discipline preferred. Exp: 6-12 months |
In the Research Associate role, you have the responsibility of performing a variety of animal procedures to support company and client research projects. This includes setting up study forms, preparing procedure rooms, and labeling and shipping samples. You will also perform various procedures, such as administering drugs through different routes (oral, SC, IP, IM, IV), collecting blood/tissue samples, and performing grafting techniques. In addition to these tasks, you will operate and maintain laboratory equipment (e.g., isoflurane machine). The Research Associate will be responsible for accurate data entry. To ensure the success of the research projects, it is critical that you maintain accurate study records and assist in maintaining lab and facility inventories. As part of your role, you will be expected to complete study reports and perform routine animal health-related tasks such as changing cages or supplying food as needed. Your attention to detail and ability to follow procedures carefully will be essential to ensure the accuracy and reliability of your research results. Lastly, you may need to perform health rounds and treatments on weekends, holidays, and occasional evenings. | 1/19/2024 |
| 3368 | Distributed Bio S. San Francisco, CA Research Study Technician I Associate degree (A.A./A.S.) in animal or laboratory science or related discipline. Bachelor's (B.A./B.S.) Degree preferred. Exp: six to twelve (6-12) months |
In this role you will observe, monitor, and document the health and physical environment within the Charles River Accelerator & Development Labs (CRADL) animal facility. Conduct in vivo experiments in rodents for multiple clients to support research programs. Collaborate with the veterinary staff to ensure that the health and welfare of laboratory animals are maintained in compliance with local, state, federal and institutional guidelines, and regulations. You will handle routine handling, restraint, identification (including ear notching, tagging) and sexing of common laboratory animals. Ability to distinguish various common laboratory animal strains in accordance with standardized genetic nomenclature and phenotype identification. You will also perform technical functions required by research protocols such as assist with dilution and dosing calculations; dosing administrations (PO, SQ, IP, IM, and IV); blood collections (Submandibular, Cardiac); basic necropsy and tissue collection; tumor measurement and body weights. Assist Vet Techs and Veterinarians with follow-up checks, treatments and procedure if needed. Perform health surveillance sample collection procedures. Actively interact with research staff to provide technical assistance. | 1/19/2024 |
| 3369 | Distributed Bio Spencerville, OH In Vivo Technician II Associate (A.A./A.S.) or Bachelor’s degree (B.A./B.S.). Exp: 6 months |
We are seeking an In Vivo Technician II for our In Vivo Team at our Safety Assessment site located in Spencerville, OH. A Technician II is performing basic tasks and procedures within a team. The technician is assigned to work on study, performing and becoming more efficient in tasks required of the department training plan which may include collecting and recording data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods. The technician is usually working closely with a trainer or buddy but becoming more independent | 1/19/2024 |
| 3370 | Distributed Bio Memphis, TN Biomanufacturing Technician I - Shift C Tuesday-Friday: 11:30am-10:00pm AS or BS in a scientific field strongly preferred. Exp: Zero to 1 year |
NOTE: This position is: Shift C: Tuesday thru Friday 11:30am - 10:00pm (Saturday, Sunday, Mondays off) The BioManufacturing Technician I is responsible for performing various manufacturing activities related to the start-up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to work night, weekends, and holidays. Must be able to meet physical requirements established in this job description. | 1/19/2024 |
| 3371 | Distributed Bio Newark, DE Molecular Technologist-1 Sequencing Associates Degree in Microbiology or related discipline required. Bachelors Degree preferred. Exp: 0-3 years |
Charles River Labs is seeking a Molecular Technologist for our Microbial Solutions site located Newark, DE. This position is Monday - Friday 10:00am to 6:30pm. The Molecular Technologist 1 will process customer samples in the microbiology laboratory utilizing the various technology platforms including but not limited to bacterial 16S rDNA and fungal ITS2 sequencing, MALDI-TOF mass spectrometry and ribotyping. Ensure adherence to regulatory requirements and GMP compliance. | 1/19/2024 |
| 3372 | Distributed Bio Memphis, TN Biomanufacturing Technician I - Shift A Sun - Wed 7:30am - 6:00pm 1 AS or BS in a scientific field required. Exp: Zero to 1 year |
The Biomanufacturing Technician I is responsible for performing various manufacturing activities related to the start-up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to meet physical requirements established in this job description. The hours are as follows: Shift A: Sun – Wed, 7:30am – 6:00pm (Thursday, Friday and Saturdays off) | 1/19/2024 |
| 3373 | Distributed Bio Ashland, OH Technician II, Formulations Bachelor’s degree (B.A./B.S.) in a relevant field. Exp: no experience |
A Technician II will prepare basic to complex dosing material and samples for vehicles, solutions, suspensions, diets, and dispensations independently with some oversight. Hours for the position are 9:00am-5:30pm Mon -Fri with potential overtime and/or weekend work. | 1/19/2024 |
| 3374 | Element Biosciences San Diego, CA Research Associate, Surface Chemistry Bachelor’s degree in chemistry, materials science, biochemistry, bioengineering, physics, or similar fields. Exp: 0-2 years |
We are seeking a Research Associate, who has a curious mind and a great desire to learn new techniques in new areas of study to join our interdisciplinary research team. You will be learning experiment design pertaining to surface coating characterization assays, explore optimal surface coating process and support custom surface production needs. The preferred candidate will have scientific research lab experience, demonstrated by any combination of prior curricular, extracurricular undergraduate research lab work, scientific paper, poster, or presentations. | 1/19/2024 |
| 3375 | EMD Serono Kankakee, IL Process Engineer Bachelor’s degree in Biology, Chemistry, or other Scientific discipline. Exp: 1+ years |
MilliporeSigma in Kankakee, IL is hiring a Process Engineer. In this role, you will identify KPIs to enhance processing and efficiencies. You will also assess new technologies to enhance production capabilities as well as reduce variation within the processes. | 1/19/2024 |
| 3376 | EMD Serono Sheboygan Falls, WI Associate Quality Control Chemist (Laboratory) Bachelor's Degree in chemistry, biochemistry,?chemical engineering or other life science discipline. Exp: 1+ year |
The Associate Quality Control Chemist will perform routine assignments using existing procedures and evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. | 1/19/2024 |
| 3377 | EMD Serono St. Louis, MO Associate Quality Scientist Bachelor’s Degree in Chemistry, Biochemistry, Biology, or other life science discipline. Exp: 1+ year |
Within the Life Sciences division of Millipore Sigma (CTDMO), the Associate Scientist (QC) position will perform quality control activities in support of GMP products at our Cherokee site. The position is within the Analytical Testing team. The job responsibilities include analytical testing and other activities in support of GMP manufacturing. The position will report to the QC Supervisor. | 1/19/2024 |
| 3378 | EMD Serono St. Louis, MO Associate Quality Scientist Bachelor's Degree in Cemistry, Biochemistry, Biology, or other life science discipline. Exp: 1+ years |
As an Associate Quality Scientist, you will be responsible for reviewing the documentation and data generated for analysis of GMP products at our Cherokee site. This review may include data supporting raw materials, in-process, and/or final products. You will be responsible for verifying that documentation and raw data meet good documentation requirements, are technically acceptable, all calculations are appropriate, and specifications are met. Additional expectations may include the review of new or updated procedures for both technical soundness and allowance for appropriate documentation. Review of audit trials, data integrity and GDP. Shift: Monday-Friday 2:00PM to 10:30PM. | 1/19/2024 |
| 3379 | EMD Serono St. Louis, MO Analytical Scientist Master’s Degree in Chemistry, Biochemistry, Engineering, or other scientific discipline. Exp: 1+ years' |
MilliporeSigma is looking for an Analytical Scientist to add to the team at our Cherokee site. In this role, you’ll be working in the Contract Testing, Development, and Manufacturing Organization (CTDMO) within the Life Sciences group of MilliporeSigma. This role will serve as an individual contributor in the Process and Analytical Development organization. You will be involved in working in a lab setting on analytical method development and optimization for external customers in the field of Antibody Drug Conjugates (ADC). The role will require problem solving, working within project timelines, and contributing to documentation for method qualification and transfer into GMP manufacturing and quality control organizations. This role will be reporting to Rodney Zollars. | 1/19/2024 |
| 3380 | EMD Serono St. Louis, MO Analytical Scientist Master’s Degree in Chemistry, Biochemistry, Engineering, or other scientific discipline . Exp: 1+ years' |
MilliporeSigma is looking for an Analytical Scientist to add to the team at our Cherokee site. In this role, you’ll be working in the Contract Testing, Development, and Manufacturing Organization (CTDMO) within the Life Sciences group of MilliporeSigma. This role will serve as an individual contributor in the Process and Analytical Development organization. You will be involved in working in a lab setting on analytical method development and optimization for external customers in the field of Antibody Drug Conjugates (ADC). The role will require problem solving, working within project timelines, and contributing to documentation for method qualification and transfer into GMP manufacturing and quality control organizations. This role will be reporting to Robert Guilmett. | 1/19/2024 |
| 3381 | EMD Serono Sheboygan Falls, WI Associate Production Scientist - 12 Hour Night Shift Bachelor’s Degree in Chemistry, Chemical Engineering, or other life science discipline. Exp: 1+ years |
The Associate Production Scientist at MilliporeSigma will manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. | 1/19/2024 |
| 3382 | Endo Pharmaceuticals Rochester, MI Microbiologist II Master of Science degree in microbiology, biology or related field. Exp: 1+ year’ |
Performs Quality laboratory microbiological analyses of materials including water testing, finished product testing, raw material testing, and method validation. Supports laboratory investigations of moderate scope and complexity while abiding by GMPs and GLPs. Has working knowledge of, and stays current with, regulatory guidance and compendia relevant to laboratories and pharmaceutical manufacturing. | 1/19/2024 |
| 3383 | Foxx Life Sciences Londonderry, NH Product Manager Lab, must be local Bachelor’s Degree in an appropriate Engineering discipline such as Mechanical, Biomedical or Chemical Engineering. Exp: 1 – 3 years |
POSITION SUMMARY: The product manager will interact with sales, marketing, Engineering and Leadership teams to provide strategic oversight to develop, launch, and grow new product offerings and solutions. Product manager works in a fast-paced environment. They are organized, can dynamically prioritize short-term and long-term business needs and are driven to work at the intersection of science and business. | 1/19/2024 |
| 3384 | Frenova Renal Research Ogden, UT Biocompatibility Engineer I Bachelor's Degree in related Engineering or scientific discipline required Exp: 0 - 2 years' |
The entry level Engineer will participate in designing, executing, and championing research and development activities of Fresenius' products. As a member of a tech team, the Engineer I environment is mentored - with oversight from higher level Engineers to complete pre-defined work. The Engineer I may be involved in quality planning, internal audits, data collection and analysis, specification development and review and design review and qualification. The Engineer I will work with cross-functional teams to develop, commercialize, and maintain high quality. | 1/19/2024 |
| 3385 | Fresenius Kabi Melrose Park and Chicago, IL Scientist I Possess a B.S. in Chemistry, Biology or related physical science. Exp: 1-4 years |
The Scientist I is responsible for an intermediate level of expertise in analytical chemistry, chromatographic methods of analysis and instrumentation, including troubleshooting. Independently executes protocols, verifications, method transfers in support of senior level personnel. Directs and provides guidance to associate scientists. | 1/19/2024 |
| 3386 | Fresenius Kabi Melrose Park and Chicago, IL Scientist I Possess a B.S. in Chemistry, Biology or related physical science. Exp: 1-4 years |
The Scientist I is responsible for an intermediate level of expertise in analytical chemistry, chromatographic methods of analysis and instrumentation, including troubleshooting. Independently executes protocols, verifications, method transfers in support of senior level personnel. Directs and provides guidance to associate scientists. | 1/19/2024 |
| 3387 | Fresenius Kabi Melrose Park and Chicago, IL Associate Scientist (Nights) BS/BA degree in Science or related field. -or- AS/AA degree. Exp: BS: 0+ years; AS: 1-3 years |
The Associate Scientist is responsible for collection and testing of routine environmental monitoring samples within aseptic processing fill lines, Isolator fill line, compounding, sterility suite, and component preparation areas for aseptic lines (Building A) and clean rooms areas in new expansion Building B. Collect and test utility samples such as WFI, clean steam and compressed gases. Monitors environmental conditions in laboratory areas during test sessions. Reports testing results and documents in compliance with cGMP and GLP standards. Provides support to Scientist, Lead Scientist, and Supervisor. Prepares media, reagents, sanitizing solutions and equipment for use in testing. | 1/19/2024 |
| 3388 | Bio-techne Minneapolis, MN Quality Assurance Specialist B.S degree in Biology related disciplines. Exp: 0 to 5 years |
The responsibilities of this position are to engage and support various improvement projects for Document Control (Label design and document writing, routing, approval etc) and Quality Assurance activities, including but not limited to Supplier Management, Non-Conformance, CAPA and Change Management etc. | 1/8/2024 |
| 3389 | Bio-techne Minneapolis, MN Research Associate Bachelor’s degree in the biological sciences or equivalent. Exp: 0 to 2 years |
The Bioassay Quality Control department provides team members the opportunity to practice and learn a variety of laboratory techniques. This position is responsible for performing protocol-defined bioassays on proteins and antibodies to demonstrate the activity of a product. The position requires maintenance of cell lines and isolation of primary cells for use in the assays. Good Manufacturing Practice (GMP) documentation and workflow is required in this position. | 1/8/2024 |
| 3390 | Bio-techne Minneapolis, MN Quality Technician, Hematology QC Lab MLT/MLS degree, bachelor’s degree in biology, or related field of study. Exp: 0-1 year |
This position will require setup, maintenance, basic troubleshooting, and operation of Hematology analyzers. This position will test hematology products for homogeneity during the bottling process by following established methods. The expectation for this position is to set up and test product on all laboratory instruments and troubleshoot as necessary within 12 months of hire. This position will adhere to safety regulations. Understand the basic ISO protocols and other applicable standards. Perform additional duties as assigned. | 1/8/2024 |
| 3391 | Bio-techne Minneapolis, MN Advanced Research Associate, QC Bioassay Master’s degree om the biological sciences or equivalent. Exp: 0 to 2 years |
The Bioassay Quality Control department provides team members the opportunity to practice and learn a variety of laboratory techniques. This position is responsible for performing protocol-defined bioassays on proteins and antibodies to demonstrate the activity of a product. The position requires experience with ELISAs, PCR, Western Blotting, and cell culture, including maintenance of cell lines and isolation of primary cells for use in the bioassays. Good Manufacturing Practice (GMP) documentation and workflow is required in this position. | 1/8/2024 |
| 3392 | Bio-techne Minneapolis, MN Advanced Research Associate Bachelor’s degree in Biology, Biotechnology, Biochemistry or equivalent. Exp: 0 to 2 years |
In this position you will build custom made-to-order kits for our rapidly growing Luminex product line, including qualification of assay components, formulation of intermediates, and preparation for packaging. | 1/8/2024 |
| 3393 | Bio-techne San Jose, CA Process Engineering Technician - Instruments Associate degree or equivalent in a relevant technical field (e.g., electrical engineering, mechanical engineering, or similar). Exp: Entry |
We are seeking a skilled and detail-oriented Process Engineering Technician to join our team. In this role, you will be responsible for supporting the development, testing, and maintenance of complex electro-mechanical instruments used in our manufacturing processes. Your expertise will be crucial in ensuring the efficient operation and optimization of these instruments, contributing to the overall success of our organization. | 1/8/2024 |
| 3394 | Bio-techne Minneapolis, MN Advanced Research Associate, Mammalian Cell Culture Bachelor’s degree in a biological science. Exp: 0 to 2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for recombinant protein production, media and supplement preparation, and additional duties as assigned. This position requires a Sunday through Thursday workweek. | 1/8/2024 |
| 3395 | Camber Spine King of Prussia, PA Associate Project Engineer Bachelor’s degree in Mechanical Engineering (preferred), Biomedical Engineering, or other relevant technical discipline. Exp: 0-3 years |
The Associate Project Engineer will be involved with legacy and new product projects, including project planning, execution, while adhering closely to project timeline and budget. | 1/10/2024 |
| 3396 | Cambrex Marlborough, MA Clean Room Analyst - Microbiological Environmental Monitoring Entry Level: Associate’s degree in Microbiology or related field; Expert Level: Bachelor’s degree or higher in Microbiology or related field. Exp: 12 months |
Our Clean Room Services team is looking for both entry level and veteran Environmental Monitoring Analysts that are passionate about leveraging their talents to provide an outstanding customer experience. If you’re interested in receiving excellent training and working as part of a team of experts with opportunities for growth, you’ll be a great fit in our strong company culture. As a Cleanroom Services Analyst you will perform environmental monitoring and cleanroom qualifications within controlled environments. You will travel to regional client sites to provide your expertise with equipment, procedures, policies and regulations to ensure that their cleanrooms meet the requirements for safe manufacturing of medical devices, pharmaceuticals and other patient products. | 1/10/2024 |
| 3397 | Advanced Sterilization Products Malvern, PA Associate Scientist, Bioassay Methods Development Master’s degree in Biology, Pharmacology. Immunology, Biochemistry or a related scientific discipline is preferred. Exp: 1 year |
The Associate Scientist, Bioassay Methods Development, will be responsible for the development of cell-based bioassays and binding assays to be used as Quality Control (QC) potency assays and in support of structure-function and biological characterization studies, to better understand mechanism of action for new molecular entities in clinical development and for commercial products. The individual will be accountable for method development, qualification, validation and transfer activities as well as the evaluation of new technologies. | 1/10/2024 |
| 3398 | Caris Life Sciences Phoenix, AZ Molecular Technologist - Solid Tumor (2nd & 3rd Shift) Bachelor’s degree in a science related field. Exp: Less than 1 year |
The Molecular Technologist is responsible for performing various molecular techniques that include, but are not limited to, formalin-fixed paraffin-embedded tissue macro-dissection, RNA/DNA extractions, PCR, DNA methylation analysis, equipment maintenance, laboratory inventory, sample tracking, ordering supplies and receiving packages. This position works under the direction of the supervisor and follows standard laboratory procedures and policies. | 1/11/2024 |
| 3399 | Caris Life Sciences Phoenix, AZ Technician - Digital Pathology Operations Associate degree with preferred major in Biological and/or Physical Sciences: or, an equivalent combination of education and experience. Exp: 1+ years |
The technician is responsible for the overall slide-scanning functions of the clinical laboratory including the routine operation and basic troubleshooting of the Whole Slide Scanners, retrieval of glass slides to be digitized, QC by visual inspection of the generated Whole Slide Images, and the testing of new software solutions to support the department. This position works under the direction of the supervisor and follows standard laboratory procedures and policies. | 1/11/2024 |
| 3400 | Caris Life Sciences Phoenix, AZ Molecular Technologist - Liquid Profiling Bachelor’s degree in a science field is required. Master’s degree in a science field is preferred. Exp: 1+ years |
The Molecular Technologist – Liquid Profiling is responsible for performing various molecular techniques that include, but are not limited to, blood processing and buffy coat extraction, RNA/DNA extractions, PCR, DNA methylation analysis, Next-Generation Sequencing, equipment maintenance, laboratory inventory, sample tracking and receiving packages. This position works under the direction of the supervisor and follows standard laboratory procedures and policies. | 1/11/2024 |
| 3401 | Catalog Boston, MA Associate Computational Biologist, R&D – Future Technologies B.S. or M.S. in computational biology, molecular biology, biomedical engineering, or a related discipline. Exp: 1+ years |
CATALOG, a Boston-based pioneering startup, is making significant strides in the field of data storage and computation by harnessing the power of DNA. DNA, known for its millennia-long stability, unrivaled information density, and cost-effective replicability, offers revolutionary potential for latency-tolerant high-density data storage and massively parallel computation. We're seeking a motivated Associate Computational Biologist with an interest in synthetic biology to join our interdisciplinary team and contribute to the development of CATALOG's DNA-based data storage and computation platform. | 1/11/2024 |
| 3402 | Catalog Boston, MA Research Associate or Senior Research Associate, DNA Computing BS or MS in biology, molecular biology, biochemistry, or a related discipline. Exp: 1+ years |
We are actively seeking a Research Associate or Senior Research Associate with a solid grounding in molecular biology or chemistry. In this role, you'll be instrumental in helping to build CATALOG's innovative DNA-based data storage and computation platform. You'll collaborate with our dynamic team of computer scientists and biologists, developing novel storage and computing architectures and translating them into scalable chemical operations. Your work will contribute to the optimization of a molecular instruction set that underpins the world’s first DNA storage and computing platform. | 1/12/2024 |
| 3403 | Catalog Boston, MA Research Associate/Senior Research Associate Tech Ops BS or MS in biology, molecular biology, biochemistry, or a related discipline. Exp: 1+ years |
We are actively seeking a Research Associate or Senior Research Associate with a solid grounding in molecular biology or chemistry. In this role, you'll be instrumental in helping to build CATALOG's innovative DNA-based data storage and computation platform. You'll collaborate with our dynamic team of computer scientists and biologists, developing novel storage and computing architectures and translating them into scalable chemical operations. Your work will contribute to the optimization of a molecular instruction set that underpins the world’s first DNA storage and computing platform. | 1/12/2024 |
| 3404 | Cellares South San Francisco, CA Cell Therapy Manufacturing Specialist Bachelor’s Degree or diploma in a scientific or related field is required. Exp: 1+ years |
We are seeking an innovative and highly motivated Cell Therapy Manufacturing Associate to join our Process Sciences team who will contribute significantly to the development and manufacture of our advanced cell therapy manufacturing platform. The primary focus of this position will be to support manufacturing operations, as well as day-to-day lab operations. This is a hands-on position that will train in Process Development, Analytical Development, and/or MSAT prior to joining the Manufacturing Group. Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows. | 1/12/2024 |
| 3405 | Cenetron Diagnostics Milwaukee, WI Tissue Recovery Specialist - Full-time Associate's Degree degree from an accredited college or university in a related healthcare field required. Exp: 1-3 years |
Under the direction of the Supervisor, the Tissue Recovery Specialist (TRS) is responsible for the surgical recovery and acquisition of tissue from donors from referring agencies. | 1/12/2024 |
| 3406 | Cenetron Diagnostics Milwaukee, WI Organ Recovery Specialist - Surgical Tech Associate's Degree or Bachelor’s Degree from an accredited college or university in a related healthcare field required. Exp: 1-3 years |
Under the direction of the Supervisor, Recovery Services the Organ Recovery Specialist is responsible for coordinating, assisting, and performing many of the key aspects related to the surgical recovery process of organ donation. | 1/12/2024 |
| 3407 | Cenetron Diagnostics Indianapolis, IN Associate Technologist Laboratory Bachelor's Degree from an accredited college or university in biology, chemistry, molecular biology, immunology, clinical laboratory science, medical Exp: 1+ years |
Under direct supervision by department leadership, performs CLIA regulated and clinical contract research testing. Interacts at a basic level with customers, providing a high level of customer service to resolve customer concerns about sample acceptability and results. Supports preparation of laboratory reagents and routine maintenance of laboratory equipment . | 1/12/2024 |
| 3408 | Cenetron Diagnostics Milwaukee, WI Associate Technologist Laboratory - Molecular Oncology and Genetics Laboratory Bachelor's Degree from an accredited college or university in biology, chemistry, molecular biology, immunology, clinical laboratory science, medical Exp: 1+ years |
Under direct supervision by department leadership, performs CLIA regulated and clinical contract research testing. Interacts at a basic level with customers, providing a high level of customer service to resolve customer concerns about sample acceptability and results. Supports preparation of laboratory reagents and routine maintenance of laboratory equipment . | 1/12/2024 |
| 3409 | Cenetron Diagnostics Wauwatosa, WI Research Technologist II - Deininger Lab Bachelor's Degree from an accredited college or university in biology, chemistry or equivalent scientific discipline required. Exp: 1-3 years |
Develops, improves, and implements laboratory techniques and performs complex experiments and/or tests to contribute to the timely and accurate completion of the research project(s). | 1/12/2024 |
| 3410 | Cenetron Diagnostics Milwaukee, WI Technologist Laboratory HLA - $3,500 sign on bonus!!!! Bachelor's Degree from an accredited college or university in biology, chemistry, molecular biology, immunology, clinical laboratory science, medical Exp: 1-3 years |
Under supervision by department leadership, performs CLIA regulated and clinical contract research testing. Interacts with customers, providing a high level of customer service to resolve customer concerns about sample acceptability and results. Supports preparation of laboratory reagents and routine maintenance of laboratory equipment. Supports the training of junior and peer staff members. Performs higher level interpretation of testing results and test panels. | 1/12/2024 |
| 3411 | Cenetron Diagnostics Wauwatosa, WI Research Technologist - Dr. Dipa Lab Bachelor's Degree from an accredited college or university in biology, chemistry, scientific discipline or equivalent combination of education and exp Exp: 1-3 years |
Under the direction of the Principal Investigator, performs laboratory assays and complex experiments to elucidate novel research questions. | 1/12/2024 |
| 3412 | Champions Oncology Rockville, MD Formulations Technician I BS degree in chemistry, pharmacology, or related field.preferred. Exp: 1 year |
The Formulations Technician will support in vivo oncology research studies in mice. Duties and responsibilities include: Receive, distribute, and disposition test compounds, vehicles, and reagents. Formulate test compounds, vehicles, and reagents. Record study data within the laboratory information management system. Read, understand, and adhere to study protocols. Perform general study preparation and organizational activities, including sample tube labeling, supply organization and stocking, and laboratory organization. Willing to work the following schedule: Friday, Saturday, Sunday, Monday and Tuesday - weekly 11:00am to 7:30pm | 1/12/2024 |
| 3413 | Champions Oncology Rockville, MD Research Associate I, Cell Culture In-Vivo BS degree. Exp: 0- 2 years |
The research associate will perform cross-functional laboratory assays with a focus on in vitro/In vivo studies. Assist in the development and execution of novel assays including collecting and processing data. | 1/12/2024 |
| 3414 | Champions Oncology Rockville, MD Research Technician, Support Team BS degree in animal science, biology, pharmacology, or related field preferred. Exp: 3 to 6 months |
A Research Technician on the Support Team provides general technical support for in vivo oncology studies in mice. | 1/12/2024 |
| 3415 | Champions Oncology Rockville, MD Laboratory Animal Care Technician BS degree in biology, pharmacology, or related field. Exp: 0 - 1+ years |
Support in vivo oncology studies in mice as a member of the Vivarium Operations Team. Duties and responsibilities: Provide animal care including handling, receipt and husbandry procedures Provide animal care including feeding and watering with food and water consumption monitoring Conduct animal observation for general health and overall well-being Clean equipment, rooms and facility according to a schedule devised by senior personnel; including floor sweeping and washing, cage washing and sterilization, and waste removal Document and initial required information in relevant room and log books Material and supply distribution and waste handling Record data using laboratory information management systems | 1/12/2024 |
| 3416 | Champions Oncology Rockville, MD Animal Research Technician I, Study Services BS degree in animal science, biology, pharmacology, or related field. Exp: 1 year |
Support in vivo oncology research studies in mice as a member of the Study Services Team. Duties and responsibilities: Perform in-life technical procedures on mice, including handling, restraint, body weight measurement, tumor volume measurement with calipers or imaging device, compound administration, blood collection, and euthanasia. Record study data within the laboratory information management system. Read, understand, and adhere to study protocols. Perform general study preparation and organizational activities, including sample tube labeling, supply organization and stocking, and laboratory organization. Work weekends and holidays on rotating basis. | 1/12/2024 |
| 3417 | Cisbio Boston, MA Lab Equipment Support Specialist Associates Degree in a Science/Engineering Field or Bachelor’s degree in a Science/Engineering Field. Exp: AS: 1-2 years; BS: 0+ years |
Enhance the existing LAMP infrastructure to track equipment preventative maintenance (PM). Service work will be performed by LAMP/OEMs and customer Facilities engineers. Support System Admin functions Provide the following compliance support activities: Enter all PM and corrective maintenance (CM) service requests and reports in customer logbook (ELN). Confirm each maintenance event receives a signed service report (electronic preferred). Review documents for accuracy. Confirm MS performance checks are done at least monthly, compile results and distribute to staff. Compile service information as needed to support internal QA and agency audits. Manage pipet calibration with record keeping in customer ELN. Generate out of calibration impact memos if there is a pipette calibration failure for customer review and approval. Maintain balance inventory and coordinate with the CUSTOMER MIC centre to support service/calibration report archival by the CUSTOMER assigned personnel. Escalate to customer corporate management if there are issues getting the appropriate support. Confirm Fume hoods/enclosures are PMed on schedule by the customer assigned personnel. Escalate issues to customer’s corporate management. PH meter maintenance – check calibration, electrode storage, and buffer expirations monthly. | 1/12/2024 |
| 3418 | Cisbio Collegeville, PA Chemical Management Specialist Bachelor's degree. Exp: 1+ years |
Performs efficiency studies (assays) and pre-clinical exploratory safety studies. Performs testing of clinical, research and quality control proficiency; evaluates instruments. Evaluates and analyzes clinical research data. Coordinates activities of associates and investigators to ensure compliance with protocol and overall clinical objectives. Manages storage of research samples. | 1/12/2024 |
| 3419 | Cisbio Bothell, WA Lab Support Coordinator Associates degree. Exp: 1+ years' |
Serve as point of contact for customer lab staff, facilitating and coordinating laboratory needs and activities. This role will work closely with other teams to seamlessly deliver lab support services. Coordinate the working lab environment daily and oversee all stock items in and near the labs including but not limited to glassware, lab coats, PPE, consumables. Occasionally support / coordinate waste removal from labs, ensuring use of waste streams with appropriate third-party vendors. Act as the liaison for escorting third-party vendors to customer lab staff for maintenance and/or repairs visits. Meet regularly with key stakeholders (lab staff, service providers, management) to identify, review and resolve issues in a timely manner and/or escalate as necessary. Regularly engage with the customer and PerkinElmer staff to ensure quality and compliance within the laboratory. Collaborate with customer line safety reps to ensure a high level of safety is maintained in the lab. Provide updates and timely communication to lab users on service work requests. Provide area walkthrough for new members of customer staff and visitors. Once certified, provide coordination of a 5S (Sort, Set in Order, Shine, Standardize, Sustain) lean service. Required to cross-train and provide back-up to other lab support areas. Complete relevant paperwork according to principles of Good Documentation Practice. Subject Matter Expert (SME) on various support needs across different buildings/floors/locations. | 1/12/2024 |
| 3420 | Coating Place Verona, WI QC Analytical Chemist - FP Team (1st Shift) Bachelor’s degree in Chemistry or related field. Exp: 1+ years |
1st Shift Position 8:00am - 4:30pm, Mon - Fri The primary purpose of the QC Analytical Chemist is to provide support to the Production and Formulations Departments by analyzing pharmaceutical and/or cleaning samples. Support will be provided by analyzing samples using various procedures including, but not limited to, internal procedures, specifications, and analytical methods; compendial monographs, client procedures, and miscellaneous protocols. The QC Analytical Chemist is expected to understand basic internal procedures and conduct analyses with some supervision after training is complete. In addition, support is provided by ensuring the essential job functions of this position are completed as part of the daily and/or weekly schedule. | 1/12/2024 |
| 3421 | Codexis Redwood City, CA Bioprocess Development Downstream Research Associate III Master’s degree in Biochemistry, Biological Science, Chemical or Biomolecular Engineering, or related discipline. Exp: 0-3 years |
The Bioprocess Development Downstream Research Associate III is responsible for designing, performing, and analyzing experiments to establish, understand, and optimize enzyme purification processes. The Research Associate will also be responsible for communicating technical data and contributing to tech transfer activities for external manufacturing of cutting-edge enzymes for nucleic acid synthesis. This position will be based on-site in Redwood City. | 1/12/2024 |
| 3422 | Codexis Redwood City, CA Process Development, Research Associate II BS or equivalent in Chemical Engineering, Biology, Biochemistry or relevant scientific field. Exp: 1 year |
The Process Development Research Associate II will join the Process Chemistry group which is part of the R&D department. Successful candidates will be a part of a dynamic and enthusiastic team responsible for development, scale up and tech transfer of the ECO Synthesis™ platform. The individual will be working with a high performing team with day-to-day laboratory workflows and operations to help with design, optimization, and analysis of ECO Synthesis™ technology. The position is an on-site role located at our Redwood City facility full time. | 1/12/2024 |
| 3423 | Cognate Bioservices Seattle, WA Research Associate I B.S. in either animal science or similar discipline preferred. Exp: 6-12 months |
In the Research Associate role, you have the responsibility of performing a variety of animal procedures to support company and client research projects. This includes setting up study forms, preparing procedure rooms, and labeling and shipping samples. You will also perform various procedures, such as administering drugs through different routes (oral, SC, IP, IM, IV), collecting blood/tissue samples, and performing grafting techniques. In addition to these tasks, you will operate and maintain laboratory equipment (e.g., isoflurane machine). The Research Associate will be responsible for accurate data entry. To ensure the success of the research projects, it is critical that you maintain accurate study records and assist in maintaining lab and facility inventories. As part of your role, you will be expected to complete study reports and perform routine animal health-related tasks such as changing cages or supplying food as needed. Your attention to detail and ability to follow procedures carefully will be essential to ensure the accuracy and reliability of your research results. Lastly, you may need to perform health rounds and treatments on weekends, holidays, and occasional evenings. | 1/12/2024 |
| 3424 | Cognate Bioservices S. San Francisco, CA Research Study Technician I Associate degree (A.A./A.S.) in animal or laboratory science or related discipline. Bachelor's (B.A./B.S.) Degree preferred. Exp: six to twelve (6-12) months |
We are seeking a Research Study Technician I for our Insourcing Solutions Department located in South San Francisco, CA. In this role you will observe, monitor, and document the health and physical environment within the Charles River Accelerator & Development Labs (CRADL) animal facility. Conduct in vivo experiments in rodents for multiple clients to support research programs. Collaborate with the veterinary staff to ensure that the health and welfare of laboratory animals are maintained in compliance with local, state, federal and institutional guidelines, and regulations. You will handle routine handling, restraint, identification (including ear notching, tagging) and sexing of common laboratory animals. Ability to distinguish various common laboratory animal strains in accordance with standardized genetic nomenclature and phenotype identification. You will also perform technical functions required by research protocols such as assist with dilution and dosing calculations; dosing administrations (PO, SQ, IP, IM, and IV); blood collections (Submandibular, Cardiac); basic necropsy and tissue collection; tumor measurement and body weights. Assist Vet Techs and Veterinarians with follow-up checks, treatments and procedure if needed. Perform health surveillance sample collection procedures. Actively interact with research staff to provide technical assistance. | 1/12/2024 |
| 3425 | Cognate Bioservices Mattawan, MI Research Technician - Pharmacokinetics & Acute Toxicology 1 1 Bachelor’s/Master’s. Exp: 1+ years |
We are seeking an experienced Research Technician for our Pharmacokinetics & Acute Toxicology Team located in Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. | 1/12/2024 |
| 3426 | Cognate Bioservices Mattawan, MI Research Analyst I - Immunochemistry Bachelor's degree (BA/BS). Exp: 0+ years |
We are seeking an Research Analyst I for our Immunochemistry at the site located in Mattawan, MI. The following are responsibilities related to the Research Analyst I: The Immunology and Immunochemistry disciplines support large molecule drug development using ligand binding assays (LBA), such as enzyme-linked immunosorbent assay (ELISA), to measure large molecules and their immune responses. The main types of assays include Pharmacokinetic (PK) assays to measure drug and Immunogenicity assay to measure anti-drug antibodies (ADA) and neutralizing antibodies (NAb). Other assay types also performed are branched DNA (bDNA) and cell-based assays. An array of platforms are used to support these assays that include spectrophotometer, Meso Scale Discovery (MSD), Luminex and Gyrolab. Utilizing these platforms/assays, the teams are responsible for the method development, validation and routine sample analysis in both the regulated and non-regulated space of non-clinical and clinical studies. | 1/12/2024 |
| 3427 | Cognate Bioservices Newark, DE Molecular Technologist-1 Sequencing Associates Degree in Microbiology or related discipline required. Bachelors Degree preferred. Exp: 0-3 years |
Charles River Labs is seeking a Molecular Technologist for our Microbial Solutions site located Newark, DE. This position is Monday - Friday 10:00am to 6:30pm. The Molecular Technologist 1 will process customer samples in the microbiology laboratory utilizing the various technology platforms including but not limited to bacterial 16S rDNA and fungal ITS2 sequencing, MALDI-TOF mass spectrometry and ribotyping. Ensure adherence to regulatory requirements and GMP compliance. | 1/12/2024 |
| 3428 | Bausch & Lomb Greenville, SC Microbiology Technician III 2nd Shift BS in Biology, Microbiology or related life science. Exp: 1+ years |
Execute microbiological testing in support of but not limited to Environmental/Water/Bioburden monitoring, Media and lab supplies preparation, Sterility Testing and Microbial Identification. Conducts tests for in-process and finished products as well as raw materials using aseptic techniques. Compliance with all applicable procedures and practices to include local and global SOP’s, product test procedures, safety, USP, ISO, GMP, and applicable governmental regulations. | 1/2/2024 |
| 3429 | Bausch & Lomb Tampa, FL Microbiology Technician III Bachelor’s degree in microbiology, Biology, or equivalent Life Science required. Exp: 1-2 years |
Perform routine and non-routine microbiological testing and environmental monitoring (EM) in support of sterile manufacturing operations. | 1/2/2024 |
| 3430 | Bausch & Lomb Tampa, FL Microbiology Technician III Bachelor’s degree in microbiology, Biology, or equivalent Life Science required. Exp: 1-2 years |
Perform routine and non-routine microbiological testing and environmental monitoring (EM) in support of sterile manufacturing operations. | 1/2/2024 |
| 3431 | Bausch & Lomb Rochester, NY Lab Technician IV AAS in Chemistry, or related field. Exp: 1-5 years |
Monitor product quality by performing tests to support marketed and pre-marketed product formulations in accordance with SOPs and regulations. | 1/2/2024 |
| 3432 | Bausch & Lomb Rochester, NY Chemist I BS in Chemistry, or related field. Exp: 1-3 years |
The Chemist is a member of the Global Quality organization. This person is responsible to monitor product quality by performing tests to support marketed and pre-marketed product formulations in accordance with SOPs and regulations. | 1/2/2024 |
| 3433 | Bausch & Lomb Tampa, FL Chemistry Technical III B. S. in Chemistry preferred, Minimum B.A. in Chemistry or related science. Exp: 1-3 years |
Perform pharmaceutical GMP wet chemistry and instrumental analysis of raw material, in-process, finished product and stability samples in the quality control chemistry laboratory in accordance with all applicable FDA/EP/JP regulations. Assume the responsibility for the GMP, ISO, and Environmental Health and Safety procedure awareness, and compliance within the respective area. | 1/2/2024 |
| 3434 | Bausch & Lomb Tampa, FL Microbiology Technician III Bachelor’s degree in microbiology, Biology, or equivalent Life Science required. Exp: 1-2 years |
Perform routine and non-routine microbiological testing and environmental monitoring (EM) in support of sterile manufacturing operations. | 1/2/2024 |
| 3435 | Baxter Round Lake, IL Quality Lab Associate I - Stability Bachelor’s degree in Chemistry or biological science with analytical chemistry laboratory coursework. Exp: 0-1 years’ |
The position may be responsible for analytical testing, validation/verification, and/or transfer of test methods supporting parenteral products. The position will be in the Round Lake, IL Stability Laboratories within Product Quality serving multiple global businesses. This role is essential for supporting the global commercial product teams and/or product development teams. The position may collaborate with multiple functions. The individual in this position must: 1) Optimally demonstrate working technical knowledge and skills to support a variety of projects within the relevant discipline with minimal assistance. 2) Display basic technical understanding of related teams. 3) Conduct routine/ experiments with assistance. | 1/3/2024 |
| 3436 | Baxter Marion, NC Associate I, Quality Lab Master’s Degree in Natural Sciences: Chemistry preferred. Exp: 0-3 years |
Conduct qualitative and quantitative chemical analysis on raw materials, solutions, and components following approved Standard Operating Procedures and test methods in an accurate and timely manner. Ability to work under minimum supervision while meeting deadlines. | 1/3/2024 |
| 3437 | Baxter Marion, NC Quality Associate I - Plastics (8th Shift: 7pm-7am) Bachelor's degree preferred. Exp: 0+ years |
Responsible for providing Quality support and oversight via direct staff supervision or process/area responsibilities. Identify and assess regulatory and quality risks in activities and processes according to regulatory agency rules and guidelines and Baxter quality practices. | 1/3/2024 |
| 3438 | Baxter Marion, NC Quality Lab Associate I - Micro ID B.S. degree in Microbiology, Biology, or related science. Exp: 0-2 years |
Responsible for reading plates for EM, Bioburden, and special project testing and recording test results. Performs additional microbiological testing as required. | 1/3/2024 |
| 3439 | Baxter Marion, NC Quality Associate I (3rd Shift: 10pm-7am) Bachelor's degree strongly preferred. Degree in engineering or life science preferred. Exp: 1+ years |
Responsible for working with the manufacturing departments to address defects with the finished products. | 1/3/2024 |
| 3440 | Baxter Marion, NC CAPA Associate I Bachelor's degree preferred(in science or engineering preferred). Exp: 1+ years |
Will be an Investigation Owner and/or CAPA Owner and is responsible for developing and performing the investigation, identifying the root cause(s) of the event, and detailing the results of the investigation. The CAPA I will likely assist in identifying the appropriate actions to mitigate or eliminate the root causes, and in determining an Effectiveness Plan for the actions (including efficiency criteria and timeframe). | 1/3/2024 |
| 3441 | Baxter Marion, NC Quality Lab Associate II - Endotoxin Master’s Degree in biological sciences. Exp: 0-3 years |
Conduct microbiological analysis on raw materials, solution, and water samples following approved Standard Operating Procedures in an accurate and timely manner. | 1/3/2024 |
| 3442 | Becton Dickinson Tempe, AZ Manufacturing Engineering II Master’s degree in a technical field. Exp: one to three years |
This is a manufacturing engineering position for the Vascular Graft and Covered Stent Graft production facility. This position is responsible for development of process improvements and validations of Vascular Graft and covered Stent Graft production processes. This position is also responsible for the transfer of newly developed products to production. | 1/3/2024 |
| 3443 | Becton Dickinson Columbus, NE Manufacturing Unit Process Engineer Bachelors Degree in an engineering discipline or equivalent experience. Exp: no experience |
This position is responsible for supporting the manufacturing operation. This individual will develop and implement improved methods of manufacturing, procedures, and processes that result in improved efficiencies, yields, machine operations, and quality. Provides technical support to the development group for the implementation of new products or processes. | 1/3/2024 |
| 3444 | Becton Dickinson Grayson; Covington, GA Microbiology Lab Tech BS in Biological Science. Exp: 1-3 years |
The Laboratory Technician is responsible for manufacturing various bacterial antigens, antisera, Treponema product line, Myco product line, Bactrol product line, purified proteins and various solutions including but not limited to buffers, reagents growth media etc. to the finished bulk product stage. | 1/3/2024 |
| 3445 | BeiGene Hopewell, VA Purification,Technician I AS/BS/BA in science related field. Exp: 1+ years |
The Purification Manufacturing Technician I position will directly enable the initial start-up phase of the Hopewell manufacturing facility and then shift focus to hands-on execution and support of cGMP manufacturing operations. | 1/3/2024 |
| 3446 | BeiGene Hopewell, VA Cell Culture, Technician II AS/BS/BA in science related field. Exp: 1+ years |
The Cell Culture Manufacturing Technician II position will directly enable the initial start-up phase of the Hopewell manufacturing facility and then shift focus to hands-on execution and support of cGMP manufacturing operations. | 1/3/2024 |
| 3447 | Berg Framingham, MA Research Associate Bachelor’s degree in Biology, Chemistry, Biochemistry, or a closely related field of study. Exp: One (1) year |
Assist in ligand binding assay method development (MSD, ELISA) and provide technique and application support for immunoassays transferred to downstream users. Test antibody quality for purity (SDS-PAGE), specificity (Western Blot, ELISA), and concentration (Nanodrop, BCA). Conduct assay performance validation. Perform protein analysis (SDS/native-PAGE, Western Blot, and Immunoprecipitation). Develop experiment protocols and prepare SOPs. Perform laboratory experiments carefully and troubleshoot to solve problems. Meticulously document experiment results in laboratory notebooks and databases timely. Analyze, summarize, and present experimental results to managers and other team members. Prepare experiment and project reports as required. Order and stock laboratory supplies for a continuous and consistent workflow. | 1/4/2024 |
| 3448 | Bethyl Laboratories, Inc. Montgomery, TX Lab Associate BS, Bachelor of Science, or related degree. Exp: 1+ years |
In this position you will support all company mammalian cell culture needs, including both production and research and development, in support of our antibody development activities. In this position you will assist with all tasks in the cell culture core. These include, but are not limited to, maintaining cells and carrying out transient transfections for expression and purification of recombinant proteins and antibodies; culturing hybridoma cell lines for antibody production; and maintaining a cell bank of over 125 different human and rodent cell lines, processing them for flow cytometry, FFPE cell pellets and cell lysate. The successful candidate is detail-oriented, highly motivated, and willing to learn new skills. Bethyl Laboratories is nimble, market-focused and growing. If you are looking for the opportunity to be first, fast, and flexible, come join us! | 1/4/2024 |
| 3449 | BGI San Jose, CA LC/MS Research Associate - Small Molecule B.S. degree with biochemistry/chemistry major or related field. Exp: 0-2 years |
San Jose Mass Spec Lab of BGI Americas is seeking an exceptional and motivated research associate with competitive compensation. The main responsibility of this position includes, but not limited, to support the SJMS production team 1) to turn around routine customer and research projects, 2) to maintenance and operate LC-MS instrument, 3) to assist lab manager to build up metabolomics and lipidomics capability in SJMS lab, 4) to support other departments when needed. A candidate with metabolomics/lipidomics LC-MS experience is a plus; a candidate with small molecule sample prep experience is a plus. An ideal candidate will need to demonstrate that they are capable of consistently following Standard Operational Procedures (SOPs) to consistently perform sample preparation procedures for metabolomic or lipidomics analysis. A candidate with hands-on experience in HPLC, Orbitrap mass spec and working with biofluids is a plus. | 1/4/2024 |
| 3450 | BGI San Jose, CA LC/MS Research Associate - Proteomics B.S. degree with biochemistry/chemistry major or related field. Exp: 0-2 years |
BGI Americas San Jose Mass Spec (SJMS) center is seeking an exceptional and motivated research associate to join our Proteomics department at our San Jose facility. The main responsibility of this position includes, but not limited, to support the SJMS production team 1) to turn around routine customer and research projects, 2) to maintenance and operate LC-MS instrument, 3) to assist lab manager to build up additional proteomics capability in SJMS lab, 4) to support other departments when needed. An ideal candidate will need to demonstrate that they are capable of consistently following Standard Operational Procedures (SOPs) to consistently perform sample preparation procedures for proteomics and biologics characterization analysis. A candidate with hands-on experience in HPLC, Orbitrap mass spec and, working with biofluids is a plus. | 1/4/2024 |
| 3451 | BioFire Diagnostics Hazelwood, MO Mechanical Engineer Master’s Degree in Mechanical Engineering. Exp: 1+ year |
Assists in the definition, proof of concept, development, implementation and/or support of technical or business solutions by performing specific tasks within the scope of the assigned activity. Identifies issues and uses problem-solving tools to formulate the necessary activities to provide successful solutions. Ensures quality of deliverables by following the appropriate design practices and departmental procedures for design control and regulatory compliance. Creates appropriate documentation such as technical communications, reports, meeting notes and other relevant technical documentation within the role’s function. Prioritizes activities within the scope of the assignments to ensure schedules or quality of work is successfully achieved. Ability to define, review and check product Bill of Materials (BOM) structures, assembly instructions and test procedures. Works with internal department and project specific teams | 1/4/2024 |
| 3452 | BioFire Diagnostics Hazelwood, MO Lab Technician - Media Tech Bachelor’s degree in a scientific field required. Biology/Chemistry preferred. Exp: One year |
The primary purpose of this position is the timely preparation, delivery, and set-up of quality, complex chemical media to Card Production., being current on training including curriculum procedures, work station organization and cleaning, establishing a safe work environment, housekeeping and maintenance functions in the production department. | 1/4/2024 |
| 3453 | BioFire Diagnostics Salt Lake City, UT Laboratory Technologist - QC I/II Associate degree or higher in a Life Science or related field. Exp: Technologist I - 6 months |
QC Technologist I works in a cGMP environment performing quality control testing for commercial and diagnostics products. Responsibilities include conducting testing of reagents and IVD materials as well as personnel swabs. Responsibilities include working with Manufacturing, Technology Transfer and other departments for data collections and validations for new product QC qualifications, organization of quality-controlled materials used for QC testing and learning new techniques or workflow as required by new product lines. QC Technologist I is also responsible for gathering and filling out quality documents pertaining to quality control testing, generation of Non-Conformance Report (NCR) when necessary and Temporary Change Order (TCO) application. QC Technologist II will be responsible for software-assisted product release (e.g., Pouch QC Web releases). This position will work in a laboratory setting and perform a variety of scientific techniques, including spectrophotometry, PCR, pipetting, etc | 1/4/2024 |
| 3454 | BioFire Diagnostics Salt Lake City, UT Template Control Laboratory Technologist I B.S. in chemistry, biology, or a related field. Exp: 6 months |
The Template Control Laboratory Technologist (LT) works with a team that formulates DNA and RNA template control components to support the company’s in vitro diagnostic products’ research and development, manufacturing, validations, and quality control efforts. The LT-I will use established methods and techniques to maintain the lab’s DNA and RNA template inventory, perform template manipulations and verification including diluting, aliquoting, mixing, quantitative PCR, quantitative RT-PCR, and FilmArray analysis, perform template and control mix formulations, and dispense template and control mixes to dependent departments in accordance with the company’s quality system. The LT-I will receive general instruction on routine work, perform lab duties under supervision, and receive training and additional instruction for new tasks as needed. | 1/4/2024 |
| 3455 | BioFire Diagnostics Salt Lake City, UT Lab Technologist I - Oligo, Night Shift Bachelor’s Degree (BS), or working toward a degree. Chemistry, BioChemistry, and Biology preferred. Exp: 1+ years |
***SIGN ON BONUS OFFERED*** $500 on first paycheck $500 after 6 months of employment BioMerieux is seeking a Lab Technologist I to join our swing shift team that manufactures Oligonucleotides. Lab Technologists are responsible for performing a wide variety of laboratory tasks and production processes. This includes operating and troubleshooting HPLCs, DNA Synthesizers, LC/MS, liquid handling robots, and UV/Vis Spectrometry. Lab Technologists works on assignments that are routine in nature where ability to recognize deviation from accepted practice is required. Normally receives general instructions on routine work, detailed instructions on new assignments. | 1/4/2024 |
| 3456 | BioFire Diagnostics Salt Lake City, UT Research Associate I Bachelor's degree in a scientific discipline. Exp: six months' |
The Research Associate I (RA I) works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g., nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to communicate and coordinate with peers and supervisor(s) effectively and respectfully. The position requires basic laboratory technical skills, organizational skills, attention to detail, critical thinking, troubleshooting and problem-solving, and a dedication to the mission and goals of the department and bioMérieux. A Research Associate I may receive general or detailed instruction and direct supervision on general work, new procedures, and assignments | 1/4/2024 |
| 3457 | BioFire Diagnostics Salt Lake City, UT Lab Technologist I - Oligo, Day Shift Bachelor’s Degree (BS), or working toward a degree. Chemistry, BioChemistry, and Biology preferred. Exp: 1+ years |
Sunday - Tuesday from 6:00 AM - 6:00 PM + every other Wednesday Thursday - Saturday from 6:00 AM - 6:00 PM + every other Wednesday ***SIGN ON BONUS OFFERED*** $300 on first pay check $300 after 6 months of employment We are seeking a Lab Technologist I to join our team. Lab Technologists are responsible for performing a wide variety of laboratory tasks and production processes. This includes operating and troubleshooting HPLCs, DNA Synthesizers, LC/MS, liquid handling robots, and UV/Vis Spectrometry. Lab Technologists works on assignments that are routine in nature where ability to recognize deviation from accepted practice is required. Normally receives general instructions on routine work, detailed instructions on new assignments Strong pipetting skills, attention to detail, organization, and familiarity with cGMP are desired. | 1/4/2024 |
| 3458 | Biogen Research Triangle Park, NC Associate II, QC Microbiology B.S. Degree. Exp: 1 1/2 - 2 years |
Schedule: this position will work 4-day, 10-hour shift Friday-Monday from 8 AM to 6 PM. The Associate II, Quality Control is responsible for supporting key functional, tactical, and operational aspects of the QC Microbiology group at the Biogen manufacturing facility. | 1/4/2024 |
| 3459 | Biogen Research Triangle Park, NC Manufacturing Associate III Bachelor’s Degree (STEM preferred). Associate’s Degree. Exp: BS: 6 months; AS: 1 year |
Manufacturing Associates perform processing steps and manufacturing support activities in our facilities in Research Triangle Park (RTP). These teams are the backbone of our operations – each person playing a critical role in delivering our therapies to the patients who need them. This position will be in our Parenteral Filling area, and our teams operate across the following units: | 1/4/2024 |
| 3460 | Biogen Research Triangle Park, NC Manufacturing Associate (Recent Grad/Entry Level) – Upstream & Downstream Bachelor’s Degree (STEM preferred) OR Associate’s Degree OR Military training & experience and are soon to transition. Exp: Entry-Level |
This requisition represents multiple open positions in our RTP Manufacturing organization. The Talent Acquisition team continually assesses all applicants that apply through this posting and will reach out to the selected candidates to discuss current and future opportunities. | 1/4/2024 |
| 3461 | Biogen Research Triangle Park, NC Associate II, QA - Swing Shift Bachelor’s degree preferably in a field of science or biotechnology. Exp: 0-2 years |
The Quality Assurance Associate II is responsible for contributing to the oversight of key strategic, tactical, and operational aspects within Quality Assurance at the Biogen Research Triangle Park (RTP) facility. Activities include but are not limited to: review of GMP raw data for compliance, review of GMP documentation to support batch disposition, review/approval of GMP procedures, protocols and reports, GxP Quality systems-related training, identifying gaps in existing Quality systems and proposing solutions to site management. The QA Associate will perform all duties in a manner consistent with site and corporate policies, cGMP, safety, environmental and human resources policies and procedures and also adhere to all regulatory licenses and regulations, interfacing with key Quality and manufacturing customers, and coordination of investigations impacting the RTP site. The QA Associate may participate in internal compliance audits; assess and approve discrepancies from site, corporate, and regulatory guidance. The QA Associate will also ensure compliance with training policies. Please note that this is a Swing Shift position and will work a traditional 2-2-3 Manufacturing Rotation from 12pm to 12am, on a 12hr/shift schedule. There is a 10% pay differential for this position. | 1/4/2024 |
| 3462 | BioLegend Pittsburgh, PA Associate Lab Technologist Bachelor's degree in a life science discipline such as Biology, Chemistry, or Medical Technology. Exp: 0-3 year |
Our team is seeking an Associate Lab Technologist to join us in our efforts to serve patients and families around the world. | 1/5/2024 |
| 3463 | BioLegend Pittsburgh, PA Research Clinical Laboratory Scientist Bachelor’s Degree in life sciences. Exp: 1-2 years |
The research clinical laboratory scientist will assist in the validation and performance of clinical laboratory tests for the diagnosis, treatment, and prevention of disease within humans. | 1/5/2024 |
| 3464 | BioLegend Lafayette, CO Associate Scientist Bachelor's Degree in Life Sciences. Exp: 0-3 years |
Revvity has a rewarding and exciting opportunity for an Associate Scientist for our Synthetic Manufacturing laboratory. The Associate Scientist position will perform primary tasks in an ISO 9001:2015 laboratory in Lafayette, CO. Key responsibilities for this position include a wide array of duties related to the manufacturing, processing, and packaging of RNA and DNA oligonucleotides. This includes synthesis, cleaving, quality and quantity determination, purification, inventory control, and order packaging. The position will require the ability to learn and to troubleshoot various aspects of manufacturing chemistry in multiple laboratories. | 1/5/2024 |
| 3465 | LGC Biosearch Technologies Middleton, WI Associate Production Scientist, Comp Cells Associate degree in relevant life sciences field (molecular biology, microbiology, biochemistry, etc.). Exp: 1+ years |
The Associate Production Scientist will manufacture competent cells for the Company’s various product lines. The position may expand to also support manufacture of additional product lines and development of new products, applications and businesses. This position is regularly based out of the company's site in Middleton, WI, with standard hours of operation Monday-Friday (8am-5pm). | 1/5/2024 |
| 3466 | LGC Biosearch Technologies Petaluma, CA Associate Engineer, Facilities Services 4 Year Degree in Mechanical Engineering, Electrical Engineering or similar. Exp: 1+ Year |
The Associate Engineer will function as an integral part of LGC’s Engineering team and will help provide strategic vision and technical support to ensure that the facilities/utilities/equipment for LGC Biosearch’s manufacturing sites are designed and operating efficiently and safely. The primary purpose of this role is to provide engineering support and design expertise for Biosearch’s Petaluma and Novato manufacturing facilities. This individual will be involved in the design and implementation of process improvements and system maintenance. This role will support the design, engineering, commissioning, and qualification of new or modified utility equipment systems and/or GMP manufacturing process instrumentation. | 1/5/2024 |
| 3467 | Biosero San Diego, CA Mechanical Design Engineer Bachelor’s degree in Bioengineering, Mechanical Engineering, or comparable field. Exp: 1 year |
We are looking for driven Mechanical Design Engineer to join our Engineering Team and help us design world-changing laboratory automation systems and associated hardware products. In this role, you will also assist the applications and sales teams in the conceptualization of automation workcells, generate the bill of materials for projects and products, work with the procurement team and vendors to ensure all fabricated components are ordered and tracked, and generate assembly drawings and instructions for the Automation Team to build projects. | 1/5/2024 |
| 3468 | Alnylam Pharmaceuticals Cambridge, MA Associate Scientist II, RNA Synthesis Bachelor’s in Chemistry, Biochemistry, or a related field. Exp: 0-3 years |
· Design, synthesis, purification, and analysis of chemically modified oligonucleotides · Improve upon and/or develop new synthetic methods and processes to expand the current capabilities. · Utilize analytical instrumentation such as UV-Vis spectroscopy, HPLC, and/or LC-MS for the analysis of both crude and purified synthetic products. Effectively troubleshoot synthetic/process issues and independently find solutions. · Improve upon and/or develop new methods and automation for the downstream processing of synthetic oligonucleotides and their subsequent analysis/purification and annealing into siRNA duplexes. · Analyze, interpret, and organize analytical data to present to team members.· | 12/27/2023 |
| 3469 | Alnylam Pharmaceuticals Cambridge, MA Associate Scientist II, Protein Sciences BS/MS degree. Exp: 0-1 years |
We are seeking an associate scientist-II to join our protein sciences group within Medicinal Chemistry to help with production, protein chemical conjugation and development efforts. The candidate must be independent, goal oriented, technically competent, and able to efficiently work across multiple projects. We are searching for enthusiastic, innovative, and highly motivated individuals, with scientific background in protein expression, purification, protein conjugation and analytical techniques, who are comfortable working in a fast-paced entrepreneurial environment. This position is onsite and will be located at 675 W. Kendall St. Cambridge, MA 02142We are seeking an associate scientist-II to join our protein sciences group within Medicinal Chemistry to help with production, protein chemical conjugation and development efforts. The candidate must be independent, goal oriented, technically competent, and able to efficiently work across multiple projects. | 12/27/2023 |
| 3470 | Alphazyme Jupiter, FL Formulation and Order Fulfillment Technician Associates degree in life science discipline such as Molecular Biology, Biochemistry or Biotechnology. Exp: 1+ years |
Maravai LifeSciences is seeking a #MiracleMaker to join our Order Fulfillment team as a Formulation and Order Fulfillment Technician. As a Formulation and Order Fulfillment Technician you will support Alphazyme’s maintenance and production of inventory necessary for fulfilling customer demands, which includes all activities related to maintaining the responsible lab area, and assists with supporting internal demands and the management of relevant formulation and fulfillment processes through executing protocols. | 12/27/2023 |
| 3471 | Alstem Richmond, CA Research Associate B.S. or M.S. degree in Biochemistry, Molecular Biology or related discipline. Exp: 1 year |
ALSTEM is looking for a highly organized and energetic Research Associate with a B.S or M.S. degree to join its scientific team. The candidate will be responsible to work as a team at all levels which will include but will not be limited to product testing and QC, and custom service projects following SOPs and protocols to support customer workflows. | 12/27/2023 |
| 3472 | Alveo Technologies Alameda, CA Scientist I BA/BS degree in Biochemistry, Molecular Biology, Microbiology or related field. Exp: 1-3 years |
Alveo Technologies is looking for a Development and Verification Scientist I to support ongoing V&V efforts of projects in disease detection. The successful candidate will assist in planning and executing protocols / conducting experiments at the bench to meet objectives. The candidate should be able to review, understand and follow the instructions, protocols and SOPs provided by the R&D and Manufacturing departments. | 12/27/2023 |
| 3473 | Amarex Clinical Research Ann Arbor, MI Lab Technician I Associate’s degree in a physical science. Exp: 1+ years |
NSF is looking for a motivated candidate who enjoys working hands-on and on their feet to be in the Exposures or Preparations Lab as a Technician I. This position is perfect for someone looking to get lab experience and have the potential to learn and grow within a certification company. This role is to perform laboratory procedures in an accurate and timely manner and continue to expand skill base while under supervision. Depending on the circumstance, potential for flexible schedules and/or part-time if someone is in school obtaining their degree and would like this experience. | 12/27/2023 |
| 3474 | Amarex Clinical Research Ann Arbor, MI Lab Technician I Associate’s degree in a physical science. Exp: 1+ years |
NSF is looking for a motivated candidate who enjoys working hands-on and on their feet to be in the Exposures or Preparations Lab as a Technician I. This position is perfect for someone looking to get lab experience and have the potential to learn and grow within a certification company. This role is to perform laboratory procedures in an accurate and timely manner and continue to expand skill base while under supervision. Depending on the circumstance, potential for flexible schedules and/or part-time if someone is in school obtaining their degree and would like this experience. | 12/27/2023 |
| 3475 | AmbioPharm North Augusta, SC Quality Control Chemist I Bachelor’s Degree in Chemistry or life sciences. Exp: 1-2 years |
Use basic understanding and knowledge of techniques, instrumentation, and lab functions to identify problems and support the completion of work assignments. Perform Quality control raw material/ release/ stability testing. Support routine analytical testing using KF, FTIR, UV and HPLC. Adapt, maintain, and operate analytical instrumentation. Perform method transfer and validation activities with minimal supervisor guidance. Conduct all quality QC chemical tests. Involve in procedure review and propose modifications and updates. Conduct various analytical testing procedures as per QC SOPs | 12/27/2023 |
| 3476 | Amide Tech Cambridge, MA Research Associate / Senior Research Associate - Peptide Chemistry BS or MS degree or equivalent experience in chemistry, chemical engineering, biochemistry, or related field. Exp: 1+ years |
Amide is seeking an exceptional individual to join our growing team as a Research Associate/Technician. The successful candidate will be a key contributor to various research projects and be responsible for executing laboratory experiments, analyzing and reporting results, and working within a larger team on a regular basis. Applicants should be team players able to excel in a fast-paced, collaborative environment. | 12/28/2023 |
| 3477 | Amneal Pharmaceuticals Brookhaven, NY Production Engineer Bachelors Degree (BA/BS) Engineering discipline or Master Degree (MS/MA) Engineering discipline. Exp: less than one year |
The Production Engineer plans and designs methods to improve production processes. Reviews existing processes and develops solutions to increase productivity or reduce costs. Ensures compliance with approved production methods and quality standards. | 12/28/2023 |
| 3478 | Amneal Pharmaceuticals Brookhaven, NY QC Chemist I Bachelors Degree (BA/BS) in Chemistry or related field. Exp: 1+ years |
The QC Chemist I (internally titled “Scientist I, Quality Control”) is an entry-level role responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents. | 12/28/2023 |
| 3479 | Amneal Pharmaceuticals Brookhaven, NY QC Chemist I Bachelors Degree (BA/BS) Microbiology or related field. Exp: 1+ years |
The QC Chemist I (internally titled “Scientist I, Quality Control”) is an entry-level role responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents. | 12/28/2023 |
| 3480 | Amneal Pharmaceuticals Brookhaven, NY QC Chemist II Master Degree (MA/MS). Exp: 1+ years |
The QC Chemist II (internally titled “Scientist II, Quality Control”) is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. | 12/28/2023 |
| 3481 | Amneal Pharmaceuticals Brookhaven, NY QC Chemist II Master Degree (MA/MS) in Chemistry or related science discipline. Exp: 1+ years |
The QC Chemist II (internally titled “Scientist II, Quality Control”) is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. | 12/28/2023 |
| 3482 | Amneal Pharmaceuticals Brookhaven, NY QC Chemist II Master Degree (MA/MS) in Chemistry or related science discipline. Exp: 1+ years |
The QC Chemist II (internally titled “Scientist II, Quality Control”) is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. | 12/28/2023 |
| 3483 | AnaSpec Fremont, CA Synthesis Chemist I BS or above in Chemistry, Organic Chemistry, or related disciplines. Exp: 1-3 years |
The Synthesis Chemist I will perform peptide production and conduct in-process testing using Good Laboratory Practices (GLP). As a member of the Synthesis department, the Synthesis Chemist I will work closely with the Purification, QC, and Sales & Business Development departments. | 12/28/2023 |
| 3484 | AnaSpec Fremont, CA QC Chemist Bachelor's degree in Chemistry or science related field. Exp: 1+ years |
This position is responsible for performing analytical testing for various product lines, such as peptides, dyes, and unusual amino acids and ensures that the products are evaluated in a timely manner and meet all procedural requirements. | 12/28/2023 |
| 3485 | AnaSpec Fremont, CA GMP Manufacturing Chemist Bachelors in chemistry, organic chemistry, biochemistry. Exp: 1+ years |
The GMP Manufacturing Chemist will be responsible for supporting all GMP upstream and downstream peptide manufacturing related processes. The GMP Manufacturing Chemist will ensure prioritization, and proper documentation of projects. This individual will work closely with GMP downstream lead and GMP upstream lead. The GMP Manufacturing Chemist is also responsible for ensuring that the assigned tasks are completed in a timely manner. | 12/28/2023 |
| 3486 | Ansh Labs Webster, TX Scientist Master’s degree in Biological/Chemical Sciences/Biotechnology or related area. Exp: 1 year |
As a key member of the Manufacturing or R&D Department, this individual will provide critical scientific skills to assist in the development and scale-up of immunodiagnostic products on various platforms (microtiter based ELISA, magnetic particle based immunoassays, Lateral Flow assays and micro fludics based immunoassays). | 12/28/2023 |
| 3487 | Ansh Labs Webster, TX Jr. Scientist Bachelor’s degree in Biological/Chemical Sciences/Biotechnology or related area. Exp: one year |
As a key member of the Manufacturing, Research & Development and Quality Control departments, this individual will provide critical scientific skills to assist in the development, scale-up and QC testing of immunodiagnostic products on various platforms (microtiter based ELISA, magnetic particle based immunoassays). | 12/28/2023 |
| 3488 | Applied Medical Rancho Santa Margarita, CA Quality Engineer I Bachelor’s degree in an Engineering or Science, Technology, Engineering, and Mathematics (STEM) field or related education and experience. Exp: 0+ years |
Collaboration is a fundamental part of our organization's culture and is essential to our continued success. As such, the successful candidate for this position is expected to work on-site, enabling them to engage fully with colleagues and contribute to cross-functional initiatives. Therefore, the ability to work collaboratively and contribute to a positive and supportive team environment is a key requirement for this role. | 12/29/2023 |
| 3489 | Applied Medical Rancho Santa Margarita, CA CAPA Quality Engineer I Bachelor’s degree in an Engineering or Science, Technology, Engineering, and Mathematics (STEM) field or related education and experience. Exp: 0+ years |
Collaboration is a fundamental part of our organization's culture and is essential to our continued success. As such, the successful candidate for this position is expected to work on-site, enabling them to engage fully with colleagues and contribute to cross-functional initiatives. Therefore, the ability to work collaboratively and contribute to a positive and supportive team environment is a key requirement for this role. | 12/29/2023 |
| 3490 | Argonaut Manufacturing Services Carlsbad, CA Bioprocess Technician II/III Level II: Requires a bachelor's degree in a related field. Exp: 1 year |
The Bioprocess Technician is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The Manufacturing Technician is expected to fully participate in both departmental projects and any quality working teams which may be applicable. existing procedures. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. This role is 100% on-site, Monday - Friday, 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. This role is 12:00 pm - 8:30 pm with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance. | 12/29/2023 |
| 3491 | Argonaut Manufacturing Services Carlsbad, CA Formulation Technician II/III Level II: Requires a bachelor's degree in a related field. Exp: 1 year |
The Formulations Technician is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The Manufacturing Technician is expected to fully participate in both departmental projects and any quality working teams which may be applicable. existing procedures. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. This role is 100% on-site, Monday - Friday, 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. This role is 12:00 pm - 8:30 pm with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance | 12/29/2023 |
| 3492 | Argonaut Manufacturing Services Carlsbad, CA Manufacturing Technician II or III Level II: Requires a bachelor's degree in a related field. Exp: 1 year |
The Manufacturing Technician is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The Manufacturing Technician is expected to fully participate in both departmental projects and any quality working teams which may be applicable. existing procedures. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. This role is 100% on-site, Monday - Friday, 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. This role is 12:00 pm - 8:30 pm with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance. | 12/29/2023 |
| 3493 | Arraystar Rockville, MD Lab Assistant - Molecular Biology Bachelor’s degree in a relevant biological field. Exp: 1-2 years’ |
Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. Assist with the generation and updating of laboratory SOPs. Perform basic lab maintenance tasks such as ordering lab supplies, and keeping detailed lab records. Communicate with clients to obtain/verify information of their projects, orders or requests. | 12/29/2023 |
| 3494 | Artiva Biotherapeutics San Diego, CA Manufacturing Associate (Temporary) Bachelor’s degree in relevant science or engineering discipline. Exp: 1 years |
The Manufacturing Associate will support manufacturing of Artiva’s off-the-shelf cell therapy platforms in our new, state of the art, cGMP facility. The successful candidate will develop, adhere to, and optimize written procedures (SOPs) related to GMP facility operations, monitor equipment and facilities, and will play a key role in the manufacturing of cell therapies internally at Artiva. The ideal candidate will demonstrate in-depth knowledge of cGMP compliance and will be a self-starter and have the ability to work independently to achieve corporate objectives. This is a temporary position and is located at our corporate headquarters in San Diego, CA. | 12/29/2023 |
| 3495 | Astute Medical Salt Lake City, UT Research Associate I Bachelor's degree in a scientific discipline. Exp: six months' |
The Research Associate I (RA I) works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g., nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to communicate and coordinate with peers and supervisor(s) effectively and respectfully. | 12/29/2023 |
| 3496 | Astute Medical Salt Lake City, UT Template Control Laboratory Technologist I B.S. in chemistry, biology, or a related field, or hold an Associate’s degree and have exceptional lab experience. Exp: 6 months |
The Template Control Laboratory Technologist (LT) works with a team that formulates DNA and RNA template control components to support the company’s in vitro diagnostic products’ research and development, manufacturing, validations, and quality control efforts. The LT-I will use established methods and techniques to maintain the lab’s DNA and RNA template inventory, perform template manipulations and verification including diluting, aliquoting, mixing, quantitative PCR, quantitative RT-PCR, and FilmArray analysis, perform template and control mix formulations, and dispense template and control mixes to dependent departments in accordance with the company’s quality system. | 12/29/2023 |
| 3497 | Astute Medical Hazelwood, MO B-Lab Technician - Media Lab Bachelor’s degree in a scientific field required. Biology/Chemistry preferred. Exp: One year |
The primary purpose of this position is the timely preparation, delivery, and set-up of quality, complex chemical media to Card Production., being current on training including curriculum procedures, work station organization and cleaning, establishing a safe work environment, housekeeping and maintenance functions in the production department. | 12/29/2023 |
| 3498 | Astute Medical Hazelwood, MO Lab Technician - Media Lab Bachelor’s degree in a scientific field required. Biology/Chemistry preferred. Exp: One year |
The primary purpose of this position is the timely preparation, delivery, and set-up of quality, complex chemical media to Card Production., being current on training including curriculum procedures, work station organization and cleaning, establishing a safe work environment, housekeeping and maintenance functions in the production department. | 12/29/2023 |
| 3499 | Astute Medical Hazelwood, MO Lab Technician-Media Lab Bachelor’s degree in a scientific field required. Biology/Chemistry preferred. Exp: One year |
This is a 3rd shift position. The primary purpose of this position is the timely preparation, delivery, and set-up of quality, complex chemical media to Card Production., being current on training including curriculum procedures, work station organization and cleaning, establishing a safe work environment, housekeeping and maintenance functions in the production department. | 12/29/2023 |
| 3500 | Astute Medical Salt Lake City, UT Template Control Laboratory Technologist I B.S. in chemistry, biology, or a related field, or hold an Associate’s degree and have exceptional lab experience. Exp: 6 months |
The Template Control Laboratory Technologist (LT) works with a team that formulates DNA and RNA template control components to support the company’s in vitro diagnostic products’ research and development, manufacturing, validations, and quality control efforts. The LT-I will use established methods and techniques to maintain the lab’s DNA and RNA template inventory, perform template manipulations and verification including diluting, aliquoting, mixing, quantitative PCR, quantitative RT-PCR, and FilmArray analysis, perform template and control mix formulations, and dispense template and control mixes to dependent departments in accordance with the company’s quality system. | 12/29/2023 |
| 3501 | Astute Medical Salt Lake City, UT Lab Technologist I - Oligo, Day Shift Bachelor’s Degree (BS), or working toward a degree. Chemistry, BioChemistry, and Biology preferred. Exp: 1+ years |
We are seeking a Lab Technologist I to join our team. Lab Technologists are responsible for performing a wide variety of laboratory tasks and production processes. This includes operating and troubleshooting HPLCs, DNA Synthesizers, LC/MS, liquid handling robots, and UV/Vis Spectrometry. Lab Technologists works on assignments that are routine in nature where ability to recognize deviation from accepted practice is required. Normally receives general instructions on routine work, detailed instructions on new assignments Strong pipetting skills, attention to detail, organization, and familiarity with cGMP are desired. | 12/29/2023 |
| 3502 | Atalanta Therapeutics Boston, MA Associate Scientist II, Oligonucleotide Chemistry Master’s degree in Chemistry or related scientific discipline. Exp: 0-2 years |
Atalanta Therapeutics is seeking a motivated Associate Scientist to join the Chemistry team to assist with the preparation of oligonucleotides for drug discovery. The Associate Scientist will work as part of a team on various projects that are critical in advancing our research and development efforts, using specialized equipment to produce high-quality compounds and analyzing data to facilitate process optimization. This individual will deliver oligonucleotides for research experiments, help maintain and troubleshoot equipment, and collaborate with cross-functional teams in a cutting-edge laboratory environment. Successful candidates will have strong analytical and problem-solving skills with an eagerness to learn and contribute to a dynamic team environment. | 12/29/2023 |
| 3503 | Atalanta Therapeutics Boston, MA Associate Scientist II/Senior Associate Scientist, In Vivo Pharmacology Master’s degree. Exp: 0-2 years |
Atalanta is seeking a highly skilled and motivated Associate/Senior Associate Scientist to join the in vivo pharmacology group to support Atalanta’s drug discovery programs. This individual will have extensive hands-on experience in performing survival surgeries (stereotaxic or direct intraparenchymal injection preferred), pharmacological administration, brain and tissue collection, and in processing CNS tissue and molecular analysis to assess target gene and protein expression. We are seeking candidates who thrive in a team-oriented, fast-paced, and cross-disciplinary biotech environment. The Associate/Senior Associate Scientist will be responsible for assay development and execution of experiments to determine the biodistribution, pharmacodynamic properties and efficacy of oligonucleotides in research and preclinical studies supporting multiple drug discovery programs and platform discovery research. | 12/29/2023 |
| 3504 | August Bioservices Nashville, TN Manufacturing Technician I/II/III - Formulation & Component Prep BS or BA or equivalent in a biological, chemical science, engineering, or degree in another discipline. Exp: One year or more |
August Bioservices is hiring Filling/Manufacturing Associates at various position levels to work in the new aseptic manufacturing facility located in Nashville, TN. The Manufacturing Technician– Component Preparation and Formulation will operate a variety of processing and packaging equipment to prepare components for aseptic filling to include bulk formulation of aqueous and non-aqueous based products, order and receive components, dispense and formulate raw materials, manage sterilized components, operate various equipment used in the formulation process, and perform cleaning operations for process equipment and the GMP ISO 8 areas. | 12/29/2023 |
| 3505 | August Bioservices Nashville, TN Manufacturing Technician I/II/III – Filling, Lyophilization, & Terminal Sterilization BS or BA or equivalent in a biological, chemical science, engineering, or degree in another discipline. Exp: One year or more |
August Bioservices is hiring Filling/Manufacturing Associates at various position levels to work in the new aseptic manufacturing facility located in Nashville, TN. The Manufacturing Technician – Filling, Lyophilization, and Terminal Sterilization will use proper aseptic technique while performing tasks in aseptic manufacturing areas to include syringe and vial filling operations with an automated line in an RABS environment as well as routine and non-routine aseptic interventions through RABS glove ports. The technician II level will operate filling and auto loading equipment, and freeze dryers using automated control systems. The Technician will be responsible for unloading of autoclaves, performing cleaning operations for process equipment and the GMP ISO 8 areas, management of sterilized components, and coordinating with maintenance as needed. | 12/29/2023 |
| 3506 | AxoGen Vandalia, OH QC Histology Technician Associate degree in chemistry, biology, or a science/technical related field required (Bachelor’s degree preferred). Exp: 1+ years |
The Quality Control (QC) Histology Laboratory Technician will support QC Histological testing by conducting a variety of laboratory tasks. He/she will also be responsible for routine laboratory operations including maintenance, solution and media preparation, routine testing, ordering supplies, and laboratory housekeeping. The QC Histology Technician will be required to handle biohazardous materials. The successful candidate will carry out testing and evaluations according to established procedures, document results, and detail any testing observations. He/she may be responsible for incoming materials release, in process testing, and release testing. He/she will also contribute to writing reports and documenting laboratory standard operating procedures (SOPs). The successful candidate will be responsible for cleaning, disinfecting, and managing inventory of lab equipment other related duties as assigned. | 12/29/2023 |
| 3507 | Bardy Diagnostics Plymouth, MN Engineer I - R&D Disposables (Hybrid) BS in Mechanical, Plastics, Biomedical Engineering or a related field, MS preferred. Exp: 0 - 1 year |
What you'll be doing Document engineering concepts. Create, modify, and maintain design documentation per company procedures. Assist in the design and building of basic tooling, test fixtures and assembly equipment. Build prototypes and models and may operate machine tools. Understand customer needs through literature review, customer interviews, direct observation, competitive analysis, prototype evaluation, and clinical/simulated use studies. Write technical reports based on design verification analysis/testing for design changes and product design activities. Develop and execute test methods which specify measurement equipment, test set-up, measurement systems analysis, and data analysis. Identify, investigate, and solve engineering problems. | 12/29/2023 |
| 3508 | Uptake Medical Johnson City, TN Quality Control Chemist - 2nd Shift Minimum 2-year Associates Degree or 4-year BS Degree in Science. Exp: 0 - 5 years’ |
The QC Chemist 1 is responsible for assisting in supporting Quality Control Laboratory personnel as it pertains to the sampling of raw materials, purified water system, in-process materials and finished products. | 12/18/2023 |
| 3509 | Uptake Medical Johnson City, TN Associate Scientist Bachelor’s degree in Chemistry or other related discipline. Exp: 0-2 years |
Crown Laboratories, Inc. is currently recruiting for an Associate Research Scientist. The Associate Research Scientist is responsible for assisting the Research Scientist and the R&D department in the development of new products from concept to commercialization to support company growth. | 12/18/2023 |
| 3510 | Wugen St. Louis, MO Associate Scientist: CMC Process Development MS Degree in biology or related field. Exp: 1+ years |
Join a fast-paced startup based in St. Louis with the opportunity to help drive process development activities of novel therapies for treating rare diseases. The associate scientist role is part of the CMC department, and will focus on executing experiments in flow cytometry. | 12/18/2023 |
| 3511 | Abbott Sturgis, MI Assistant Chemist I, Analytical Lab (1st Shift) - Sturgis, MI Plant Science related Associates Degree or Science related Bachelor’s Degree. Exp: AS: 1 year; BS: 0+ years |
An Assistant Chemist I is responsible for testing the necessary raw ingredient, in process, and finished product as prescribed in the various quality procedures and assuring specifications and quality guidelines are met. The incumbent is responsible for producing the highest quality results while operating within the constraints of the manufacturing schedule and safety guidelines. They are responsible for maintaining good manufacturing practices and good laboratory practices. The chemist I is responsible for developing positive relations with other chemists and operators from other departments that interact with the laboratory. The incumbent is also responsible for providing timely feedback to the chemist following them, their lead chemist, and their supervisor as to the status of their area of responsibility. | 12/18/2023 |
| 3512 | Abbott Sturgis, MI Assistant Chemist I, Analytical Lab (1st Shift) - Sturgis, MI Plant Science related Associates Degree or Science related Bachelor’s Degree. Exp: AS: 1 year; BS: 0+ years |
An Assistant Chemist I is responsible for testing the necessary raw ingredient, in process, and finished product as prescribed in the various quality procedures and assuring specifications and quality guidelines are met. The incumbent is responsible for producing the highest quality results while operating within the constraints of the manufacturing schedule and safety guidelines. They are responsible for maintaining good manufacturing practices and good laboratory practices. The chemist I is responsible for developing positive relations with other chemists and operators from other departments that interact with the laboratory. The incumbent is also responsible for providing timely feedback to the chemist following them, their lead chemist, and their supervisor as to the status of their area of responsibility. | 12/18/2023 |
| 3513 | Abbott St. Paul, MN Clinical Engineer-2 Associates Degree. Exp: 1 year |
Under general supervision, responsible for designing new products and processes and improving and maintaining existing products. May execute less complex projects. Under general supervision, responsible for designing new products and processes and improving and maintaining existing products. May execute less complex projects. Under general supervision, responsible for designing new products and processes and improving and maintaining existing products. May execute less complex projects. | 12/18/2023 |
| 3514 | Abbott Irving, TX Associate Mechanical Engineer BS Mechanical Engineering. Exp: 0-2 years’ |
Individual contributor that works under limited supervision. Designs mechanical and electromechanical products and systems by developing and testing specifications and methods. | 12/18/2023 |
| 3515 | Abbott Sturgis, MI Assistant Microbiologist I (2nd Shift, Tues-Sat) - Sturgis, MI Plant Science related Associates Degree or Science related Bachelor’s Degree. Exp: AS: 1 year; BS: 0+ years |
Apply high quality scientific techniques in the microbiological analysis of raw ingredients, in-process production samples, finished product testing and environmental monitoring, to ensure that all products manufactured are fit for use Be able to work with fellow microbiologist, with a high degree of motivation, attention to important details with clear communication to all team members. This is important due to the high degree of responsibility and working within a small group where each person is relied upon highly Prioritize tasks to efficiently be completed with the most accurate results, and to communicate clearly and work together in a team environment Product testing, Environmental testing, Raw ingredient testing Documentation, Project work, Troubleshooting Media preparation/general lab work: Housekeeping Communication, Teamwork | 12/18/2023 |
| 3516 | Abbott Sturgis, MI Assistant Microbiologist I (3rd Shift) - Sturgis, MI Plant Science related Associates Degree or Science related Bachelor’s Degree. Exp: AS: 1 year; BS: 0+ years |
Apply high quality scientific techniques in the microbiological analysis of raw ingredients, in-process production samples, finished product testing and environmental monitoring, to ensure that all products manufactured are fit for use Be able to work with fellow microbiologist, with a high degree of motivation, attention to important details with clear communication to all team members. This is important due to the high degree of responsibility and working within a small group where each person is relied upon highly Prioritize tasks to efficiently be completed with the most accurate results, and to communicate clearly and work together in a team environment Product testing, Environmental testing, Raw ingredient testing Documentation, Project work, Troubleshooting Media preparation/general lab work: Housekeeping Communication, Teamwork. | 12/18/2023 |
| 3517 | Abbott St. Paul, MN Manufacturing Engineer I Bachelors of Science degree in Electrical Engineering, a related field or equivalent. Exp: 0-3 years |
This position works out of our St Paul, MN location in the Electrophysiology Medical Device division. In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. We are seeking a Manufacturing. Engineer I. This position will design and develop manufacturing processes and support production and service activities in order to meet daily production schedules while enhancing productivity, cost and product quality. Product lines supported are comprised of electronic systems used in our medical devices to better the lives of patients around the globe. | 12/18/2023 |
| 3518 | Abeona Therapeutics Cleveland, OH Manufacturing Associate MS in scientific discipline. Exp: 1-2 years |
Abeona is looking for a Manufacturing Associate to join our team in Cleveland, OH. The successful candidate will be responsible for Manufacturing initiatives supporting multiple product pipelines. The candidate will be an integral part of a fast-paced group responsible for the manufacture of retroviral vector, autologous gene-corrected cell therapies, and clinical AAV gene therapies. Responsibilities will include executing protocols and manufacturing clinical material across multiple products as well as supporting process optimization work and document generation. The ideal candidate will have experience in production of biologics in a controlled cGXP setting. Strong aseptic and cell culture technique as well as collaborative work in a team is an integral part of this position. | 12/20/2023 |
| 3519 | Abeona Therapeutics Cleveland, OH Manufacturing Associate MS in scientific discipline. Exp: 1-2 years |
Abeona is looking for a Manufacturing Associate to join our team in Cleveland, OH. The successful candidate will be responsible for Manufacturing initiatives supporting multiple product pipelines. The candidate will be an integral part of a fast-paced group responsible for the manufacture of retroviral vector, autologous gene-corrected cell therapies, and clinical AAV gene therapies. Responsibilities will include executing protocols and manufacturing clinical material across multiple products as well as supporting process optimization work and document generation. The ideal candidate will have experience in production of biologics in a controlled cGXP setting. Strong aseptic and cell culture technique as well as collaborative work in a team is an integral part of this position. | 12/20/2023 |
| 3520 | Analytical Biological Services Wilmington, DE Biorepository Technologist I (In-Sourced) Associate’s Degree in a medical or biological science is required. Bachelor’s Degree preferred. Exp: 1+ years |
Primary duties and responsibilities of the Biorepository Technologist I (In-Sourced) included but are not limited to: -Receive biospecimens including frozen, fixed, or fresh solid and liquid samples -Coordinate with shipping and receiving department to ensure all shipments are appropriately tracked -Coordinate with internal clinical study team to ensure sample and data accuracy -Communicates by written and verbal methods with related departments to assure samples arrive in the appropriate lab -Record sample quality concerns and provide feedback to collection site or central lab -Document sample information in laboratory database from source documents -Accession samples and appropriate data in the laboratories electronic data management system -Pull samples from inventory when requested by scientists for internal projects -Report and reconcile study data for management teams across departments -Provide Data management with scheduled monthly inventory reports and inventory reports upon Data managers request in a timely manner. -Upload monthly inventory reports to LIMS Labmatrix. -Organize and audit existing inventory QC and QC of sample location and data integrity -Ensure compliance with best practice guidelines, laboratory and EHS protocols, company standards and policies, standard operating procedures (SOP), and industry regulations. -Other duties as assigned | 12/20/2023 |
| 3521 | Analytical Biological Services Wilmington, DE Cell Culture Scientist BS or BA or higher degree in biological sciences. Exp: 1+ years |
- The position involves maintenance of cell culture lines to include thawing, expanding, harvesting and freezing lines. - Strict quality control guidelines of all products coming from cell culture must be monitored and adhered to. - Proper and aseptic maintenance of cell culture and production laboratory is required. - The Scientist must be able to effectively communicate with team members and clients of our progress with products and services and be able to respond quickly and accurately to client inquiries and requests. - Record keeping, excellent organizational skills and the ability to multitask are a must. | 12/20/2023 |
| 3522 | Absorption Systems Baltimore, MD Research Assistant undergraduate with a Life Sciences degree. Exp: entry-level |
We are seeking Research Assistants to join our Baltimore, MD clinical team! As a Research Assistant, you will be responsible for a variety of clinical research activities, ensuring that established protocols are followed, maintaining study protocol integrity, monitoring participant's status and safety, and playing a significant role in the training of clinical staff. We are conveniently located on the University of Maryland BioPark campus and provide paid parking for all employees. We have 12-hour day shifts, night shifts, and weekend shifts available. If you're seeking an entry-level role in Research, please apply. | 12/20/2023 |
| 3523 | Abveris Portland, OR Manufacturing Associate Associates or Bachelors degree in Biology, chemistry or related field is desirable. Exp: 1+ years |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations team in Wilsonville, OR. The Manufacturing Associate will produce various DNA and plasmid products, focusing on molecular and cellular biology, as well as running analytic techniques in the high-throughput/highly-automated lab according to established SOPs, along with working with sensitive equipment and following good manufacturing practices. Candidates must also be a team player, neat and highly organized, able to work in a cleanroom environment and foster safe work practices. The Manufacturing Associate will perform basic reagent handling, chemistry and molecular biology workflows in a highly automated, high-throughput manner and will be responsible for the manufacture and analysis of a variety of custom DNA based intermediates and products across Twist Bioscience’s proprietary process workflow to meet the Twist production forecast and timelines. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast paced start-up environment. The Manufacturing Associate will be responsible for the production of custom gene based products and/or various intermediates according to established SOPs and complete manufacturing batch records to contribute to the daily production schedule. | 12/20/2023 |
| 3524 | Abveris Portland, OR Manufacturing Associate - Gene Production Associates or Bachelors degree in Biology, chemistry or related field is desirable. Exp: 1+ years |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations team in Wilsonville, OR. The Manufacturing Associate, Gene Production, will produce various DNA and plasmid products, focusing on molecular and cellular biology, as well as running analytic techniques in the high-throughput/highly-automated lab according to established SOPs, along with working with sensitive equipment and following good manufacturing practices. Candidates must also be a team player, neat and highly organized, able to work in a cleanroom environment and foster safe work practices. The Manufacturing Associate will perform basic reagent handling, chemistry and molecular biology workflows in a highly automated, high-throughput manner and will be responsible for the manufacture and analysis of a variety of custom DNA based intermediates and products across Twist Bioscience’s proprietary process workflow to meet the Twist production forecast and timelines. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast paced start-up environment. The Manufacturing Associate will be responsible for the production of custom gene based products and/or various intermediates according to established SOPs and complete manufacturing batch records to contribute to the daily production schedule. | 12/20/2023 |
| 3525 | Abveris South San Francisco, CA Manufacturing Associate, NGS TE Production Associates or Bachelors degree in Biology, chemistry or related field is desirable. Exp: 1+ years |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations Team in South San Francisco. The Manufacturing Associate, NGS TE will perform basic molecular biology workflows in a highly automated, high-throughput manner and will be responsible for the manufacture of variety of custom oligonucleotide products. The ideal candidate will be able to work independently, be very neat and organized, have the ability to follow established SOPs and complete manufacturing batch records to contribute to the daily production schedule. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast paced start-up environment. The Manufacturing Associate will be responsible for the production of custom gene based products and/or various intermediates according to established SOPs and complete manufacturing batch records to contribute to the daily production schedule. They will uphold standards as defined by the manufacturing process, work on continuous improvement and have good time management resulting in efficiency, and work in a safe manner. | 12/20/2023 |
| 3526 | Abveris Portland, OR Manufacturing Associate - Reagent Production Associates or Bachelors degree in Biology, chemistry or related field is desirable. Exp: 1+ years |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations team in Wilsonville, OR. Shift: Tuesday-Saturday (3:00pm-11:30pm PST) The Manufacturing Associate will perform basic reagent handling, chemistry and molecular biology workflows in a highly automated, high-throughput manner and will be responsible for the manufacture and analysis of a variety of custom DNA based intermediates and products across Twist Bioscience’s proprietary process workflow to meet the Twist production forecast and timelines. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast paced start-up environment. | 12/20/2023 |
| 3527 | Abveris South San Francisco, CA Associate Engineer Bioinformatics, Biopharma Libraries BS or MS in Computer Science, Bioinformatics, or related scientific/engineering field. Exp: 0 - 1 years |
Twist Biopharma is seeking an Associate Bioinformatics Engineer to develop and integrate workflows, analyses, and computational tools involved in the production and research of antibodies and proteins. While you have a broad interest in biotech and related scientific technologies, you also understand that computer science resources must be utilized to reach the scale required for our most complex solutions. The ideal candidate has computational/software/bioinformatics experience, and a basic knowledge of biology, DNA, antibody development, or protein sciences. He or she is comfortable with Python and JavaScript and will assist in the development of cutting-edge machine-learning applications, databases, and reports using modern tools, software development techniques, and coding best practices. | 12/20/2023 |
| 3528 | Abveris South San Francisco, CA Research Associate II, Process Development Research Associate: BA. Research Associate II: MSc. Exp: RA: 0-2 years; RAII: 0-2 years. |
The Research Associate II will interface between R&D and Operations to establish new processes at scale for DNA-based products in manufacturing. You will develop and support the production team’s custom DNA-based applications and assays for synthetic biology including high-throughput probe generation through robust experimental design. The ideal candidate will be driven and will do what it takes to keep manufacturing on track and constantly improving in a fast-paced startup environment. | 12/20/2023 |
| 3529 | Associates of Cape Cod East Falmouth, MA Quality Control Analyst I B.S. degree in a relevant scientific discipline. Exp: 0-2+ years |
In this role you will perform chemical and/or biological assays of commercial product raw materials, production intermediate and bulk samples, finished product, environmental monitoring samples, process and cleaning validation samples. Assays are qualitative, quantitative and investigational in nature and are performed in compliance with cGMP, ACC SOPs, and FDA Analyst has working knowledge of relevant QC techniques, policies and procedures to perform QC tasks and document results. Analyst receives minimal supervision on routine assignments and detailed instructions on new assignments. | 12/20/2023 |
| 3530 | Adaptimmune Therapeutics Philadelphia, PA Quality Analytical Science and Technology Associate Scientist Bachelor’s degree in molecular biology, biomedical sciences or related specialties. Exp: 1+ years |
The purpose of this role is primarily to perform scientific work to support the Quality Control and Analytical Science and Technology team of analytical method and assay validations of Adaptimmune’s T-cell platform analytics. An Associate Scientist is broadly expected to support the team with the following duties. | 12/22/2023 |
| 3531 | Adare Pharmaceuticals Philadelphia, PA Analytical QC Chemist I Bachelor’s degree in chemistry, Biology, biochemistry, or related scientific field. Exp: 0-2 years’ |
The Analytical Chemist II is an essential part of the lab Quality team and will be expected to perform physical and chemical testing of intermediate and finished products according to written procedures. | 12/22/2023 |
| 3532 | Admera Health South Plainfield, NJ Associate Scientist I/II Bachelor’s degree in Biological Sciences or M.S. in Biological Sciences. Exp: BS: 1-3 years; MS: 1 year. |
Responsibilities: • Preparing solutions and reagents for performing assays on the bench. • Perform Next Generation Sequencing-based genomic assays on different workflows (few listed below): o RNAseq o Whole Genome Sequencing o Whole Exome Sequencing | 12/22/2023 |
| 3533 | Aimmune Therapeutics Dublin, OH Chemistry Technician BS in Related Science. Exp: 0-5 years |
Position Summary: The Technician position may undertake performance and documentation of routine tasks related to sample processing and assays using written operating procedures, standard laboratory methods and/or basic laboratory techniques, functions and equipment. To conduct specific procedures and tests both within and outside of the laboratory requiring the use of applied knowledge and practical skills learned from on-the-job experience; modify or adapt techniques to fit special needs or problems; to calculate data from routine tests to final results and to evaluate such results for accuracy where expected findings are not precisely defined, but sufficient guidelines exist for reference; to assist with and occasionally perform specialized and non-routine tests and assays, and to maintain records of such work; to coordinate and plan assigned work with other technicians and scientists. This position requires the following schedule pattern: Tuesday - Saturday 7:00am - 3:30pm OR Thursday - Monday 7:00am – 3:30pm | 12/22/2023 |
| 3534 | Aimmune Therapeutics Leonia, NJ Chemist B.S. in chemistry preferred. Exp: 1+ years |
Position Summary: The Chemist position is responsible for performing routine laboratory procedures in a quality control laboratory. Duties are performed under general supervision. Must be familiar with basic laboratory equipment and techniques. Responsibilities are focused on less complex testing and support functions. | 12/22/2023 |
| 3535 | Aimmune Therapeutics Dublin, OH Quality Technician undergraduate degree in closely related science preferred (i.e. Microbiology, Chemistry, Biology, et al.) Exp: 1 year |
Position Summary: This position performs and documents routine tasks related to sample processing and assays using written operating procedures, standard laboratory methods, and/or basic laboratory techniques, functions and equipment. The position conducts specific procedures and tests within the laboratory requiring the use of applied knowledge and practical skills learned from on-the-job experience; modify or adapt techniques to fit special needs or problems; to calculate data from routine tests to final results and to evaluate such results for accuracy where expected findings are not precisely defined, but sufficient guidelines exist for reference; to assist with and occasionally perform specialized and non-routine tests and assays, and to maintain records of such work; to coordinate and plan assigned work with other technicians and scientists. | 12/22/2023 |
| 3536 | Aimmune Therapeutics Bayport, NY Associate Technical Services Scientist/Specialist (TAG - Bayport, NY) Bachelor’s degree in Science, Chemistry, Chemical Engineering or in a related field required. Exp: 1+ years |
The Associate Technical Services Scientist/Specialist works within our Technical Applications Group (TAG) and will assist in formulating nutritional supplement products in various forms in support of manufacturing by collecting, evaluating, analyzing and summarizing data, address manufacturing issues, evaluate new technologies and/or ingredients and seek cost savings. Adherence to Standard Operating Procedures (SOP’s) and current Good Manufacturing Practices (cGMP’s) in this role is required. This position will work onsite Monday through Friday at Nestle Health Science’s manufacturing site in Bayport, NY (Long Island area). | 12/22/2023 |
| 3537 | Aimmune Therapeutics Mechanicsburg, PA Controls Technical Specialist I | $2,000 Sign On Bonus Eligible Associate’s Degree in a technical discipline Exp: 1+ years |
At Nestlé Purina PetCare, we’re a “safety first” culture, driven by a zero accident, zero defect, zero waste mentality. As a Controls Technical Specialist I, you’ll be responsible for troubleshooting, maintaining and enhancing the accuracy, reliability and system control’s data credibility of PLC and PC-based automation systems. In this role, you will oversee PLC upgrades and wiring modifications on production equipment and work directly with our maintenance team to troubleshoot and support production line modifications. As a Controls Technical Specialist I at our Mechanicsburg facility, you will enjoy competitive pay, $2,000 sign-on and retention bonus, premium pay, up to 5% quarterly bonus, $500 Lifestyle Spending each year, full health benefits, 401k match, generous PTO, excellent maternity/paternity leave and so much more! | 12/22/2023 |
| 3538 | Aimmune Therapeutics Flagstaff, AZ Associate Staff Engineer Bachelor’s Degree in Engineering or related field. Exp: 1+ year |
As an Associate Engineer, you will support the development of factory masterplans to align with Nestlé Purina long-term business objectives. You will have the opportunity to leverage your leadership skills while working with cross-functional teams at the corporate and factory levels. You will assist with delivering high value through technical scope development with supported justification, while adhering to project standards and strategies. Additionally, you will work on project submittal requirements and ensure quality while working closely with Nestlé Purina stakeholders. | 12/22/2023 |
| 3539 | Aimmune Therapeutics Solon, OH Product Development Associate BS or MS degree in Food Science, Food Engineering, Chemical Engineering, Packaging Science, Packaging Engineering, Mechanical Engineering, or related Exp: 0-3 years |
You will work hands-on the with our Pilot Plants and Factories, and Manufacturing facilities to deliver on the Innovation & Renovation (I&R) business objectives. You will dig into recipe (re)formulation, rapid pro-typing, and manage vendor relationships/interactions. You will help to build consumer insights and be the face of our products in cross-functional settings with commercial teams like Marketing, Sales, Finance. | 12/22/2023 |
| 3540 | Alkermes Wilmington, OH QC Analyst I Bachelor of Science degree in Chemistry or related scientific field. Exp: 1+ years |
The QC Analyst I performs testing of samples submitted to the laboratory in a cGMP compliant manner, as well as according to approved written procedures. The QC Analyst I may be required to write or revise SOPs, analytical procedures, or other analytical documentation at the discretion of quality control supervisory staff. | 12/22/2023 |
| 3541 | Alkermes Wilmington, OH Temp-QC Analyst-Microbiology Wilmington, OH, United States Bachelor's in science, preferably in Biology / Microbiology / Biotechnology or Biochemistry, required. Exp: 1+ year |
QC Analyst I must have broad knowledge of microbiology techniques within the laboratory required for the routine support of the microbiology laboratory operations. In this role the Analyst will be a fully functional member of the team responsible for testing and data entry for finished product, in-process samples, stability samples, clinical materials and raw material release in a cGMP regulated environment | 12/22/2023 |
| 3542 | Alkermes Wilmington, OH QC Analyst I/II Bachelors Degree in Chemistry. Exp: 0-2 years |
The position requires the individual to perform routine/non-routine physical, chemical, and in-vitro assays of clinical, commercial, process and cleaning validation samples, and process development samples to support Manufacturing. Performs physical and/or chemical analyses of product to ensure stability. Participates in the preparation of investigations, summaries and reports. Reviews data obtained for compliance to specifications and reports abnormalities. Revises and updates standard operating procedures as needed. May perform special projects on analytical and instrument problem solving. | 12/22/2023 |
| 3543 | Alkermes Wilmington, OH Temp-Manufacturing Associate-Bulk-2nd Shift Associates degree or higher in a science/technical discipline. Exp: 0-1 year |
Perform all necessary operation activities in bulk manufacturing. These activities include but are not limited to the following: Equipment Cleaning, Equipment Set-up, Equipment/Automation Operation, and Batch Processing. Reads and follows detailed written SOPs / Procedures and detailed documentation of operations according to cGMP. Performs sample collection, equipment/process monitoring, and minor maintenance. Maintain individual training proficiency through individual Learning Management System. Other responsibilities include SOP writing and review of cGMP documentation. | 12/22/2023 |
| 3544 | Alkermes Wilmington, OH Manufacturing Associate-Bulk 2nd Shift Associates degree or higher in a science/technical discipline. Exp: 1+ year |
Perform all necessary operation activities in bulk manufacturing. These activities include but are not limited to the following: Equipment Cleaning, Equipment Set-up, Equipment/Automation Operation, and Batch Processing. Reads and follows detailed written SOPs / Procedures and detailed documentation of operations according to cGMP. Performs sample collection, equipment/process monitoring, and minor maintenance. Maintain individual training proficiency through individual Learning Management System. Other responsibilities include SOP writing and review of cGMP documentation. | 12/22/2023 |
| 3545 | Alkermes Wilmington, OH Process Engineer I/II/Lead-Filling Process Engineer I: BS degree in Engineering or technical discipline. Exp: 0-2 years |
Support and assist in the manufacture of pharmaceutical products for commercial and clinical supplies. Scale-up and transfer formulations/processes to production facility, design and recommend equipment purchases, write and execute qualification/validation protocols. Troubleshoot automated equipment for pharmaceutical formulation and packaging. Identify and implement process/equipment improvements (utilizing Change Control system) to reduce waste and increase process reliability. Support of manufacturing management in periodic review of existing and new revisions to manufacturing documentation in regard to, but not limited to, Operability, Technical accuracy (technical reviews), Compliance, Process Robustness. Perform process and equipment evaluation (FMEA, etc) to identify risks and weaknesses in new and current processes, Write or revise SOPs and other GMP documentation in support of new or changed manufacturing processes in cooperation with appropriate manufacturing personnel, Assure the resolution of deviations, corrective actions, action items from Change Control systems, and any audit non-compliance items. Develop and implement SOPs in support of new and upgraded processes, Develop and implement effective training of manufacturing personnel related to technical transfer and process upgrades, represent manufacturing on process design teams, Champion projects as they move into and through the manufacturing areas, Provide regular updates to manufacturing management on the status and issues involved in projects. | 12/22/2023 |
| 3546 | Alliance Pharma Malvern, PA Associate Scientist I- Immunoassay BA/BS or higher. Exp: 1-2 years |
• Prepare reagents, standards, and control samples • Analyze samples using various techniques specific to department • Perform method validation or qualification • Operate analytical equipment • Maintain analytical equipment • Ensure lab area is clean and inspection ready at all times • Remove lab waste • Record tasks in accordance with Good Documentation Practices (GDP) • Understand and apply regulatory requirements; GLP, GCP, 21CFR Part 11 • Follow applicable SOPs and procedural documents • Review and evaluate data results | 12/22/2023 |
| 3547 | Alliance Pharma Malvern, PA Assistant Scientist II BA/BS or higher. Exp: 1-2 years |
Prepare reagents, standards, and control samples · Analyze samples using various techniques specific to department · Operate analytical equipment · Maintain analytical equipment · Ensure lab area is clean and inspection ready at all times · Remove lab waste · Record tasks in accordance with Good Documentation Practices (GDP) · Learn and apply regulatory requirements; GLP, GCP, 21CFR Part 11 · Follow applicable SOPs and procedural documents · Learn how to review and evaluate data results · Other tasks as assigned | 12/22/2023 |
| 3548 | Prominex San Diego , CA Research Associate I/II Master’s degree in Science Exp: 0-2 years |
We are looking for an enthusiastic and dedicated Research Associate to implement and execute analytical and scientific experiments to drive Product Development. Demonstrates high degree of organization and planning and the ability to apply scientific principles to plan out and execute experiments involving a variety of laboratory methods. This individual demonstrates technical proficiency, high degree of organization and planning and the ability to apply scientific principles. | 12/12/2023 |
| 3549 | RayzeBio Indianapolis, IN Microbiologist BS/MS in Biology, Microbiology, or other Life Science related field. Exp: up to five years |
Reporting to the Asst. Manager of Microbiology, the Microbiologist will help support the establishment of a new Environmental Monitoring/Microbiology laboratory which supports RayzeBio’s Radiopharmaceutical manufacturing facility in Indianapolis. The Microbiologist will be providing support for the commissioning, qualification, and validation of cleanroom environments and equipment and the associated environmental monitoring program. Upon establishment of the laboratory and program, the position will support the environmental monitoring and microbiological release testing of manufactured radiopharmaceuticals to support RayzeBio’s clinical and commercial programs. | 12/13/2023 |
| 3550 | RayzeBio Indianapolis, IN Radiopharmaceuticals Production Operator (I/II) Associate’s or Bachelor’s Degree in a STEM field is preferred. Exp: 1 – 4 years’ |
The Radiopharmaceuticals Production Operator will be an integral part of bringing RayzeBio’s innovative drug products to patients in need. As the Production Operator, you will play an active role in daily operations, striving to ensure each batch is right the first time and that the production area is kept in order at our manufacturing site in Indianapolis IN. You will be responsible for the production of RayzeBio drug products, strictly complying with good manufacturing practice and aseptic requirements. Additionally, you will be the front line in ensuring compliance with radiation safety requirements on the production floor. As RayzeBio expands the production site and its portfolio of new products, you will support validation work for future company initiatives, and support management with internal projects and new hire training. The Radiopharmaceuticals Production Operator will report directly to the Production Manager. Operator level will be evaluated with experience and qualifications. | 12/13/2023 |
| 3551 | RayzeBio Indianapolis, IN Quality Control Chemist BS/MS in Chemistry, Science, or relevant field. Exp: up to five years |
Reporting to the Sr. Manager of Quality Control, the Quality Control Chemist will help support the establishment of a new Quality Control laboratory which supports RayzeBio’s Radiopharmaceutical manufacturing facility in Indianapolis. The Quality Control Chemist will be responsible and/or providing support for the installation, commissioning, qualification, and validation of analytical and radiochemical equipment for the QC lab. Upon establishment of the laboratory and program, this position will utilize a wide range of analytical and radiochemical analyses to support the advancement and release of novel targeted radiopharmaceuticals from the R&D phase through clinical development to GMP commercial radiopharmaceutical production. Specifically, the quality control chemist will support the release of manufactured radiopharmaceuticals to support RayzeBio’s clinical and commercial programs. | 12/13/2023 |
| 3552 | MacroGenics Rockville, MD Research Associate II Master’s degree in a scientific discipline. Exp: 0+ years |
The Research Associate II / Associate Scientist I position will support preclinical development of MacroGenics antibody-drug conjugates (ADC) through cell line engineering and molecular biology support. This position will independently develop and engineer cell lines, and conduct cell-based, molecular, and biochemical assays which contribute to the ADC research and development pipeline. | 12/13/2023 |
| 3553 | MacroGenics Rockville, MD Animal Health Technician I Bachelor’s degree in scientific discipline. Exp: 0+ years |
The Animal Health Technician I is responsible for executing animal care duties and responsibilities that enable us to support rapid advancement of preclinical programs. | 12/13/2023 |
| 3554 | Rockland Immunochemicals Pottstown, PA Associate Scientist/Scientist I, Molecular Biology Bachelor’s degree in biological sciences, biochemistry, or a closely related scientific field. Exp: 1-2 years |
Responsibilities include: RNA and DNA amplification and digestion (for transfection or transformation) as well as immunofluorescence assays, antibody validation (SDS, WB, Analytical SEC) Purification and characterization of recombinant protein targets using AKTA, ion exchange, affinity and size exclusion chromatography. Perform laboratory experiments independently or with other team members, including immunoassays, column production, affinity chromatography, and product handling Bacterial and mammalian expression of recombinant proteins, protein characterization including but not limited to: SDS page, western blot, dot blot, ELISA, Immunofluorescence Candidate is expected to perform basic mammalian cell culture Maintain laboratory space, equipment, and inventory in an appropriate and professional manner Lab housekeeping and solutions and materials restocking. Present data and final report suitable to deliver to clients Perform other duties as assigned | 12/13/2023 |
| 3555 | Rockland Immunochemicals Pottstown, PA Associate Scientist, Quality Control Bachelor’s degree in biochemistry, pharmacology, molecular biology, cancer biology, or related field or associate degree in similar field. Exp: 1+ years |
Rockland Immunochemicals is a worldwide leader in the development and commercialization of antibodies and antibody based tools. To further enable innovative biomarker development for drug discovery and diagnostic applications, we also offer highly customized solutions to meet basic, applied and clinical research demands. We are seeking a talented and highly motivated team player as an addition to our Quality Control Department. Join the group and apply your experience in the QC environment. | 12/13/2023 |
| 3556 | Toxikon Madison, WI Research Lab Analyst Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1+ years |
Labcorp Drug Development is the leading global Clinical Research Organization. We have an exciting career opportunity for an Analyst on our BioAnalytical team in Madison, WI. The Analyst is focused on the extraction of biological samples (Protein Preciptation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. This position is a day shift with a flexible start time. | 12/15/2023 |
| 3557 | Toxikon Greenfield, IN Research Assistant I - Cell Based and Immunology Team BS/BA degree in science or related field. Exp: 1+ years |
Executes basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 12/15/2023 |
| 3558 | Toxikon Greenfield, IN Research & Development Scientist Minimum of Bachelors in an appropriate scientific field. Exp: 1+ years |
Scientific Knowledge and Technical Expertise: Technical expertise in one or more of the following scientific disciplines is desired: Cell Culture and Cell-Based Potency Assays ELISA Statistics/Biostatistical experience pertaining to biopotency assays and/or In Vivo Relative Potency Assays. Virology qPCR Flow Cytometry Additional experience in Western blotting, Capillary IsoElectric Focusing, Capillary Electrophoresis, UV Spectroscopy and HPLC/ UHPLC is a plus. | 12/15/2023 |
| 3559 | Toxikon Greenfield, IN Research Assistant I BS/BA/BSc degree in science or related field. Exp: 1+ years |
Executes basic Molecular BioA (Mol BioA) laboratory procedures under the oversight of experienced personnel. | 12/15/2023 |
| 3560 | Toxikon Greenfield, IN Research Assistant I-Protein Chemistry BS/BA degree in science or related field. Exp: 1+ years |
In this role you will learn to execute basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 12/15/2023 |
| 3561 | Toxikon Research Triangle Park, NC Cytogenetics Technologist - 2nd Shift Bachelor's degree in Biology, Chemistry, Medical Technology or a related science. Exp: 1+ years |
Are you an experienced Medical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Cytogenetics Technologist in RTP, NC. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". Integrated Oncology, a LabCorp Specialty Testing Group, provides reference anatomic pathology, hematopathology and molecular pathology testing services to hospitals, health systems and independent oncology practices. Integrated Oncology is focused on providing world class solutions to better the lives of patients living with cancer. The schedule for this position will be 2nd Shift (Tuesday-Saturday 1pm-9:30pm) | 12/15/2023 |
| 3562 | Toxikon Greenfield, IN Laboratory Scientist Mammalian Cell Culture BA/BS in biology, molecular biology, microbiology, immunology, or a related field. Exp: 1+ years |
As a Laboratory Scientist, you will analyze samples for various compounds and components, run assays, perform mammalian cell culture, flow cytometry and perform data analysis and QC data in compliance with standard operating procedures (SOPs) and regulatory agency guidelines. | 12/15/2023 |
| 3563 | Trevigen Minneapolis, MN Advanced Research Associate, QC Bioassay Master’s degree om the biological sciences or equivalent. Exp: 0 to 2 years |
The Bioassay Quality Control department provides team members the opportunity to practice and learn a variety of laboratory techniques. This position is responsible for performing protocol-defined bioassays on proteins and antibodies to demonstrate the activity of a product. The position requires experience with ELISAs, PCR, Western Blotting, and cell culture, including maintenance of cell lines and isolation of primary cells for use in the bioassays. Good Manufacturing Practice (GMP) documentation and workflow is required in this position. | 12/15/2023 |
| 3564 | Trevigen Minneapolis, MN Research Associate, Molecular Biology Master’s degree in Molecular Biology or equivalent. Exp: 0-2 years |
The responsibilities of this position are to assist the protein product development team in the area of recombinant protein expression. This includes the preparation of eukaryotic expression vectors, cell culture, and screening procedures. The successful candidate will perform various techniques such as DNA preps, sub-cloning, mammalian and insect cell culture, transfections, Western blotting, ELISA, and flow cytometry. They will also prepare buffers and reagents, assist in cleaning and maintenance of the laboratory and equipment, and perform other general lab duties as assigned. | 12/15/2023 |
| 3565 | Trevigen Minneapolis, MN Research Associate Bachelor’s degree in Biology, Biotechnology, Biochemistry or equivalent required. Exp: 0 to 2 years |
In this position you will build custom made-to-order kits for our rapidly growing Luminex product line, including qualification of assay components, formulation of intermediates, and preparation for packaging. | 12/15/2023 |
| 3566 | Trevigen Waltham, MA Medical Laboratory Technologist Bachelor of Science Degree in a chemical, physical or biological science. Exp: six months |
This position is responsible for performing high-complexity CLIA testing in day-to-day operations of the laboratory. | 12/15/2023 |
| 3567 | Trevigen Minneapolis, MN Research Associate Bachelor’s degree in the biological sciences or equivalent. Exp: 0-2 years |
The responsibilities of this position are to prepare conjugated proteins, antibodies, enzymes and microparticles for both manufacturing and research. In addition, this position will be responsible for the preparation and testing of other chemistry related reagents for company personnel. Perform additional duties as assigned. | 12/15/2023 |
| 3568 | Trevigen Minneapolis, MN Research Associate Bachelor’s degree in the biological sciences or equivalent. Exp: 0 to 2 years |
The responsibilities of this position are production, bottling, and packaging of stem cell and gene therapy medias. Perform QC testing and analysis of some cell culture media. Perform cell culture of multiple cell lines. Production of components for additional stem cell, and non-stem cell kits. Skills used include cell culture, high attention to detail, strong communication and organizational skills. This will be a Tuesday through Saturday work schedule. | 12/15/2023 |
| 3569 | Trevigen Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
We are seeking an Advanced Research Associate for Bio-Techne’s Protein Purification department in Minneapolis. Our group supports 5000 different protein products used in academic research, pharmaceutical research, and all facets of biological science including: neurodegenerative diseases, stem cell research, glycobiology, developmental biology, etc. This individual will collaborate with many different departments to support the manufacturing processes of our products and contribute to the ongoing development of our growing and evolving portfolio. This position provides a potential for growth and career advancements within the company. This is a fantastic opportunity for an individual to gain problem solving and troubleshooting experience in a collaborative lab environment. This position also provides continuous learning and development, flexible working hours, and the ability to learn and apply a variety of lab techniques every day. | 12/15/2023 |
| 3570 | Tyber Medical Bethlehem, PA Quality Engineer /Senior Quality Engineer Bachelor’s degree from a four-year college or university in a related field of study. Exp: one year |
The Quality Technician organizes and runs the routine analysis of the Quality Control Department. This job is essential in ensuring the Quality Control Department meets its goals of efficiency and customer satisfaction. This individual is responsible for conducting inspection and testing procedures during manufacturing processes and receiving inspection processes to ensure the products comply with requirements. | 12/15/2023 |
| 3571 | Universal Cells Seattle, WA Research Associate II, Gene Editing MS degree. Exp: 0-2 years |
The primary purpose of the Research Associate II position is to assist with gene editing of pluripotent stem cells. This position will work primarily in a laboratory setting in collaboration with other Scientists and Research Associates. | 12/15/2023 |
| 3572 | Vala Sciences San Diego , CA Research Associate (RA)/Senior Research Associate (SRA) – Assay Development and iPSC Maintenance B.S. or M.S. in Molecular/Cell Biology, Biochemistry, Neuroscience, Bioengineering, or related. Exp: 1+ years |
We’re seeking an RA or SRA to join our dynamic assay development and induced pluripotent stem cell (iPSC) research team. The successful candidate will execute validated assays for contract research projects and assist in management and maintenance of iPSC lines. Additionally, you will work with senior scientists in the Neurobiology and Cardiology groups to plan and perform experiments for assay development to support Vala’s internal and contract research projects. You will maintain differentiated iPSC cell cultures for live cell assays using Vala’s Kinetic Image Cytometry (KIC) technology, as well as perform IF staining to assist in development of reproducible and optimized assays. You may perform differentiation of iPSC to different cell types, such as neurons, astrocytes, microglia and cardiomyocytes. You will work in a close-knit, fast-paced team environment and adapt readily to changing needs as projects and technologies evolve. | 12/15/2023 |
| 3573 | Vala Sciences San Diego , CA Research Associate (RA)/Senior Research Associate (SRA) – iPSC Manufacturing B.S. or M.S. in Cell/Molecular Biology, Biochemistry, Neuroscience, or related field. Exp: 1-2 years |
The successful candidate will manage iPSC lines and their differentiation to different cell types, like cardiomyocytes, microglia, neurons, and astrocytes. These differentiated iPSC lines will be used for internal R&D projects, commercial research contracts, and manufacture for sale. You will evaluate and validate differentiated cell lines with biomarker detection methods like ICC or flow cytometry, and investigate and characterize cellular function using Vala’s live-cell fluorescent imaging technology. You will work in a close-knit, fast-paced team environment and adapt readily to changing needs as projects and technologies evolve. | 12/15/2023 |
| 3574 | VaxCyte San Carlos, CA Associate Scientist II, Upstream Development for Protein Development and Manufacturing MS in Biology, Chemical Engineering or Chemistry/ Biochemistry. Exp: 0-2+ years |
Vaxcyte is seeking a talented and energetic Associate Scientist I/II, to join the Upstream Process Development group within the Protein Development and CMC team. Vaxcyte is developing a multi-valent conjugate vaccine, based on a novel carrier protein produced using the XpressCFTM platform. This is an exciting opportunity to join a team aiming to establish a new fermentation development lab and pilot plant at Vaxcyte. | 12/15/2023 |
| 3575 | Vector Laboratories Newark, CA Technical Application Scientist II Master’s degree in Biology, Chemistry or related life science field required. Exp: 1+ years |
The Technical Support Scientist’s primary responsibility will be to provide product and application expertise, insight and troubleshooting assistance for all Vector Laboratories’ reagents to researchers across the life sciences fields and to our distributors worldwide. Also, as a member of the commercial team, the Technical Support Specialist will help in the generation of technical material and marketing content to support promotional activities and campaigns, as well as represent the company at conferences, meetings and vendor shows as required. The successful candidate will be self-motivated, a creative thinker and a problem solver who enjoys direct interaction with people. Candidate will be a team player with strong communication, organizational, and time management skills. Previous experience in a technical support role in a life science company would be beneficial. This position reports to the Sr Director, Commercial Operations. The ideal candidate for this position will be a collaborative problem solver, working to find the best possible solution to the client’s questions and needs. The candidate should embrace opportunities to learn more about our existing and upcoming products, as well as what our competitors are releasing. This is a collaborative, team, environment. To apply for this position, please email your resume and cover letter to: talent@vectorlabs.com. | 12/15/2023 |
| 3576 | VGXI Conroe, TX UPSTREAM MANUFACTURING PROCESS TECHNICIAN Bachelor’s or Associate's degree or equivalent from college or technical school. Exp: one to three Years |
Responsible for manufacturing revolutionary clinical and commercial nucleic acid based pharmaceuticals by interfacing with manual and automated production systems and controls in cGMP manufacturing environment while maintaining areas in a state of compliance with internal quality systems. Follows standard operating procedures to operate production equipment for upstream operations. Maintains records, process and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for proficiency in assigned functional area: Upstream Manufacturing. Understands and applies biological, chemical and mechanical principles and techniques. | 12/15/2023 |
| 3577 | VGXI Conroe, TX DOWNSTREAM MANUFACTURING PROCESS TECHNICIAN Bachelor’s or Associate's degree or equivalent from college or technical school. Exp: one to three Years |
Responsible for manufacturing revolutionary clinical and commercial nucleic acid based pharmaceuticals by interfacing with manual and automated production systems and controls in cGMP manufacturing environment while maintaining areas in a state of compliance with internal quality systems. Follows standard operating procedures to operate production equipment for downstream operations. Maintains records, process and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for proficiency in assigned functional area: Downstream Manufacturing. Understands and applies biological, chemical and mechanical principles and techniques. | 12/15/2023 |
| 3578 | VGXI Conroe, TX QUALITY CONTROL TECHNICIAN Bachelor’s or Associate's degree or equivalent from college or technical school. Exp: one to three years |
The Quality Control Technician is responsible for in-process and release testing of products manufactured at VGXI. Responsibilities also include environmental monitoring of the production areas and raw material quarantine and release. Set-up, organization, and day-to-day operations of a Quality Control Lab are also required. | 12/15/2023 |
| 3579 | Viant Medical Brimfield, MA Quality Engineer Minimum of Associate’s Degree in Engineering or related technical field, with Bachelor’s Degree preferred. Exp: 0-3 years |
The primary purpose of this job is to provide Quality Engineering support for Operations to ensure that the Quality System requirements are adhered to for medical device manufacturing/operations in accordance with applicable Regulatory and Standards requirements for compliance. | 12/15/2023 |
| 3580 | Vividion Therapeutics San Diego , CA Research Associate I/II, Proteomics B.S. in Chemistry- or Biology-related field. Exp: 1-4 years |
Vividion Therapeutics is seeking a highly motivated Research Associate to help support the operation of our cutting-edge proteomics platforms. The successful candidate will have a high level of organization and attention to detail. The role will involve techniques such as cell culture, in vivo tissues processing, high throughput screening on an automated system, and protein chemistry or chemical biology. This position will help discover novel small-molecule ligands of protein targets through the execution of screens using our novel mass spectrometry-based proteomics platforms. | 12/15/2023 |
| 3581 | WaVe Life Sciences Cambridge, MA Research Associate II BS/MS in biology, biochemistry, cellular/molecular biology or related discipline. Exp: 1+ years |
Wave seeks a highly motivated biologist to join its research team in Cambridge, Massachusetts to support a rapidly expanding RNA-editing platform. This is an ideal position for an individual who is interested in working with cutting edge technologies and who thrives in a team-oriented, fast-paced, and cross-disciplinary biotech environment. The candidate should have strong technical skills, and will be responsible for designing, executing, and analyzing experiments as a member of team focused on advancing therapeutic programs and discovery research platforms. | 12/15/2023 |
| 3582 | Frontage Exton, PA Associate Scientist/Scientist, BCGT Analytical Development Master's degree in, Molecular Biology, Cell Biology, or a related field. Exp: 1-2 years |
We seek a highly skilled Associate Scientist/Scientist to join our dynamic Molecular and Cell Biology team. This role will focus on developing analytical methods supporting biologics, cell, and gene therapy modalities. The ideal candidate will possess a deep understanding of tissue culture, cell line maintenance, cell-based assays, and proficiency in molecular approaches such as DNA/RNA extraction and PCR techniques. | 12/15/2023 |
| 3583 | Frontage Exton, PA Associate Scientist Bachelor’s or master’s degree in molecular biology, cell biology, biochemistry, or a related field. Exp: 1+ years |
The Cell-based Assay Core Lab, based at our Exton headquarters, stands as a premier provider of diverse cell-based assays. These include potency assays, neutralizing antibodies assays, EliSpot, virus plaque assay, TCID50 Assays etc. We are seeking a candidate with a fundamental understanding of Cell Biology, Biochemistry, and Molecular Biology. The ideal candidate should be highly organized, self-motivated, enthusiastic about learning, and capable of managing multiple projects concurrently. | 12/15/2023 |
| 3584 | Frontage Exton, PA Associate Scientist/Scientist – Protein Biochemist BS Degree or MS Degree. Exp: 1 year |
This is a bench scientific position for a competent and hardworking scientist with experience in protein purification and/or labeling of protein reagents. The person will be responsible labeling of reagents (protein and antibodies), purification and characterization including concentration estimation, SDS-PAGE, SE-HPLC, endotoxin estimations etc. He/she will be responsible for the quality of final product, record keeping and interacting with end user. The position will require excellent communication skills, and basic computer skills. | 12/15/2023 |
| 3585 | Frontage Concord, OH Laboratory Research Technician – Full time /Concord Ohio Educational Requirements: High School/GED or above (AS & BA/BS). Exp: entry-level |
Individuals in this position support evaluation of the safety and/or toxicity of pharmaceutical and biotechnology products by ensuring the health and welfare of research animals. | 12/15/2023 |
| 3586 | Frontage Hayward, CA Research Assistant-ADME BS in biology, biochemistry and other related fields. Exp: 0-3 years |
We are looking for a highly-motivated Research Assistant to develop and conduct biochemical and cellular assays to evaluate potential therapeutics. Experience in cell line development, ELISA, PBMC biomarker, cell culture, cellular assays, gene expression is desirable. Prior experience in ADME assays including metabolite stability, drug transporter, CYP450, PPB and measurements of physicochemical properties is preferred. The candidate needs to be proficient in assay design, trouble-shooting, data analysis and working with 96-w & 384-w plate-based assays. The candidate needs to have a good understanding of drug discovery processes and experience in a discovery project is preferred. This position requires working with an interdisciplinary team of DMPK scientists, analytical chemists and pharmacologists. | 12/15/2023 |
| 3587 | Frontage Hayward, CA Research Associate-Bioanalytical M.S. degree in related scientific discipline or B.S degree. Exp: BS: 1+ years; MS: 0-3 years. |
1)Execute established protocols and methods to assay small molecule compounds, their metabolites, and impurities in various chemical and biological samples. 2)Perform data analysis on LC/MS and HPLC instruments, with the ability to identify and troubleshoot inconsistencies as needed. 3) Perform analytical, pharmacokinetic/pharmacodynamic, metabolism data analysis. 4) Conduct basic method development and validation studies. 5) Conduct trouble-shooting and instrument maintenance of LC/MS. 6) Present and discuss data internally and externally. 7) Write reports under supervision. | 12/15/2023 |
| 3588 | PCI Pharma Services Bedford, NH QA Associate I - Operations Bachelor’s Degree in a relevant scientific discipline preferred. Exp: 0-2 years |
The Quality Associate I - Operations is responsible to provide QA support real-time for GMP Manufacturing of drug product. Responsibilities include providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. Real time continuous monitoring of manufacturing related systems and processes to ensure compliance with applicable regulatory and industry standards, needed quality improvements, and safety/efficacy for phase appropriate GMP manufacture of drug products. | 12/4/2023 |
| 3589 | PCI Pharma Services Philadelphia, PA Process Engineer I Bachelor's Degree in mechanical, packaging engineering, or in a related field of study. Exp: 1-5 years |
We are looking for a dedicated process engineer to provide technical leadership for new product launches and lead continuous improvement activities. You will also identify and mitigate packaging issues for existing business through strong engineering and process improvement methods. All activities are focused around technical and operational support to production, maintenance, and support staff to include but not limited to: process improvement, equipment modification, optimization, safety, quality improvement, and increasing throughput. The process engineer will achieve this through delivery of tracking, analysis of metrics and project management. The ideal candidate will have a strong understanding and utilization of good engineering practices with the usage of lean six sigma techniques. The process engineer will also provide excellent organizational and leadership skills to determine staffing projections, equipment needs, equipment purchase, equipment installation, component layout, and line layout | 12/4/2023 |
| 3590 | PCI Pharma Services Philadelphia, PA Process Engineer I-2nd Shift Bachelor's Degree in mechanical, packaging engineering, or in a related field of study. Exp: 1-5 years |
We are looking for a dedicated process engineer to provide technical leadership for new product launches and lead continuous improvement activities. You will also identify and mitigate packaging issues for existing business through strong engineering and process improvement methods. All activities are focused around technical and operational support to production, maintenance, and support staff to include but not limited to: process improvement, equipment modification, optimization, safety, quality improvement, and increasing throughput. The process engineer will achieve this through delivery of tracking, analysis of metrics and project management. The ideal candidate will have a strong understanding and utilization of good engineering practices with the usage of lean six sigma techniques. The process engineer will also provide excellent organizational and leadership skills to determine staffing projections, equipment needs, equipment purchase, equipment installation, component layout, and line layout.**This is a second shift position. Hours are: 4pm to 12 Midnight, Monday to Friday** | 12/4/2023 |
| 3591 | PCI Pharma Services Philadelphia, PA Process Engineer I-Wkends AM Bachelor's Degree in mechanical, packaging engineering, or in a related field of study. Exp: 1-5 years |
We are looking for a dedicated process engineer to provide technical leadership for new product launches and lead continuous improvement activities. You will also identify and mitigate packaging issues for existing business through strong engineering and process improvement methods. All activities are focused around technical and operational support to production, maintenance, and support staff to include but not limited to: process improvement, equipment modification, optimization, safety, quality improvement, and increasing throughput. The process engineer will achieve this through delivery of tracking, analysis of metrics and project management. The ideal candidate will have a strong understanding and utilization of good engineering practices with the usage of lean six sigma techniques. The process engineer will also provide excellent organizational and leadership skills to determine staffing projections, equipment needs, equipment purchase, equipment installation, component layout, and line layout***This is a weekend position 6am to 6pm Friday, Saturday, and Sunday.** | 12/4/2023 |
| 3592 | PCI Pharma Services Rockford, IL Package Testing Engineer Bachelors degree in engineering and/or related discipline. Exp: 0-2 years |
The Package Testing Engineer supports PCI’s mission to provide industry-leading experience to clients, developing and commercializing solutions to optimize the delivery of lifesaving medicines and support better health outcomes for patients around the world. Reporting to the Principal Package Testing Lead, a successful Package Testing Engineer would utilize engineering skills and technical insights to evaluate, develop, test, and qualify effective packaging systems for PCI’s clients. Under the guidance of the Principal Associate, utilizing practical packaging development knowledge, effective report writing, and hands-on assembly skills, the Package Testing Engineer would support PCI’s Package Testing Services, commercial sales efforts as well as the successful commercialization of awarded packaging projects. In addition to the primary role of package testing, the incumbent would support package design and on-site prototyping projects as needed. Package Testing Engineer would support the workflows and reliability of the on-site Package Testing Lab and regularly coordinate projects with external partners. The Package Testing Engineer may engage clients, consultants, vendors, and suppliers directly to aid in the successful design and implementation of new packaging systems and products. | 12/4/2023 |
| 3593 | PCI Pharma Services Rockford, IL Serialization Engineer Bachelor's Degree in a related field. Exp: 1-5 years |
Serve as primary technical expert and principal designer/developer for all global major packaging line serialization design and integration efforts. Work closely with suppliers and internal colleagues to identify and specify complex line connectivity requirements and translate to comprehensive interface solutions specifications and delivery. | 12/4/2023 |
| 3594 | PharPoint Research Durham or Wilmington, NC Quality Assurance Auditor Bachelor’s degree (B.A./B.S.) or equivalent in a scientific, computer, or related discipline. Exp: 1-2 years’ |
Performs project and non-project quality assurance duties at PharPoint Research. Responsible for carrying out quality initiatives at the company, including but not limited to SOPs and training, computer systems validation, and Quality Management System. | 12/4/2023 |
| 3595 | PolyPeptide Group Torrance, CA Production Chemist I BS in Chemistry, Biochemistry, Biology or related science field. Exp: 1+ years |
Production Chemist is responsible for completing tasks & assignments in accordance with established processes & methodologies; synthesize peptides, intermediates, & processing from initial stage. | 12/4/2023 |
| 3596 | Poseida Therapeutics San Diego, CA Quality Control Analyst Bachelor’s degree in Life Sciences or related discipline. Exp: 1+ years |
Poseida Therapeutics, Inc. is seeking an outstanding candidate to join our Quality Control team. The Quality Control Analyst I will be a member of a dynamic team that ensures the safety of our products at various points during the manufacturing process by performing environmental monitoring, raw material and final product testing. As well as working cross-functionally with individuals and departments within the Pilot Plant Facility. | 12/4/2023 |
| 3597 | Kriya Therapeutics Morrisville, NC GMP Facilities Engineer Bachelor's degree in Engineering or related field. Exp: 1-3 years |
The GMP Facilities Engineer will be responsible for overseeing the facility's alarm response, deviation, change control, and CAPA management, ensuring compliance with Good Manufacturing Practices (GMP) in a biotech manufacturing environment. This individual will also play a crucial role in managing the Computerized Maintenance Management System (CMMS) and participation in project teams by serving as the representative of the facilities group. | 11/27/2023 |
| 3598 | Krystal Biotech Pittsburgh, PA Bioprocess Engineer Bachelor’s degree, preferably in life sciences. Exp: 1+ years |
Krystal Biotech, Inc is seeking a highly motivated and dynamic Bioprocess Engineer to support our product manufacturing at our Pittsburgh GMP facility. This role is critical to our make a meaningful difference in the lives of underserved patient populations having rare diseases. Quality, safety and on-time delivery is a must to be successful in this role! The ideal candidate will have foundational experience in upstream and/or downstream biologics or gene therapy manufacturing. | 11/27/2023 |
| 3599 | Krystal Biotech Pittsburgh, PA Manufacturing / Bioprocess Support Technician BS Degree in Biology, Engineering or related field is preferred. Exp: Entry Level |
Krystal Biotech, Inc is seeking a highly motivated Bioprocess Support Technician to support the growing Manufacturing team in Pittsburgh, PA. This role will perform a wide range of duties to support manufacturing processes in a GMP environment. | 11/27/2023 |
| 3600 | LakePharma
LakePharma
LakePharma
Camarillo, CA Microbiologist I Bachelor’s degree in Microbiology, Science or related field. Exp: 0-3 years |
Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The Quality Control Microbiologist I performs quality activities in support of product production and releases. The position performs a wide variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending and reporting results. | 11/28/2023 |
| 3601 | LakePharma
LakePharma
LakePharma
Lebanon, NJ Analytical Chemist I Bachelor’s degree in Chemistry or Chemical engineering. Exp: 1-2 year |
MAJOR DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Perform routine testing related to compendial monographs and general chapters; Saponification/Hydroxyl/Acid/Iodine Value, IR/UV analysis, Assays GC/HPLC analysis, ICP-MS analysis, Atomic Absorption spectrometry, etc. Perform measurements, computations, tabulation, and analyze results related to the testing conducted. Under the supervision of more experienced analysts, perform basic non-routine instrumental analysis and wet chemistry analysis in response to customer inquiries and projects as required. This may include but not limited to developing methods and performing method validation and verifications. Operate and maintain/calibrate laboratory equipment as per manufacturer’s recommendations and company’s Preventive Maintenance program. Maintain laboratory records related to all testing activities assuring that they are accurate and up to date. Perform other related duties as assigned. Perform all analysis and lab related duties as per cGMP. | 11/28/2023 |
| 3602 | Liquidia Morrisville, NC Manufacturing Technician B.S. degree. Exp: 0-2 year’s |
We are looking for a hands-on and experienced Manufacturing Technician. In this role, you will perform routine running of manufacturing equipment to support production and R&D efforts. Furthermore, you will provide feedback to engineering and scientific staff on process performance and ideas for process improvement. | 11/29/2023 |
| 3603 | Lygos Berkeley, CA Process Engineer B.S. in Chemical Engineer, Bioengineering, or related Engineering discipline. Exp: 1-2 years |
We are seeking a motivated Process Engineer to join our growing organization. As a key member of the pilot fermentation facility at Lygos, you will report to the Director of Fermentation and work closely with another Process Engineer on the team to support day to day operations of our pilot scale fermentations. You will support the fermentation team in maintenance and repair of fermentation equipment and contribute to the development of automation tools for the team. | 11/29/2023 |
| 3604 | Lyra Therapeutics Watertown, MA MSAT Engineer I/II Bachelor’s Degree (Engineering Preferred). Exp: 1+ years |
Our team is growing, and we are currently recruiting a Manufacturing Sciences and Technology (MSAT) Engineer I/II to support pharmaceutical operations at the Waltham and Watertown, MA sites. The focus of this position is to ensure manufacturing equipment and processes are operating as intended to meet the requirements for drug product manufacturing. This position will play a key role in delivering results in a fast paced, highly collaborative, and dynamic environment. The position will assist in the startup of a combination drug-device product from new product launch through commercial production. This involves process development, commercial process validations, technology transfers, as well as being accountable for commercial production. | 11/29/2023 |
| 3605 | Masy Biosciences Charleston, SC Environmental Monitoring Technician - 2nd Shift Bachelor’s degree preferred. Exp: 0-2 years |
The Environmental Monitoring Technician I is accounable for results in a fast-paced environment. The Level I Technician follows applicable SOPs and cGMPs to perform environmental monitoring for the facility, and may also perform simple, routine basic interpretation of environmental monitoring (EM) results, typically under supervision. This position is also responsible for hazardous waste and sanitation/cleaning of the Microbiology laboratory. The position requires strong leadership behaviors of the Alcami core competencies and non-negotatiables, as well as the functional competencies of this profile | 11/29/2023 |
| 3606 | Masy Biosciences Charleston, SC Pharmaceutical Manufacturing Technician - 1st Shift Associate’s degree preferred. Exp: 1-2 years |
The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employs acceptable techniques while working in manufacturing environments, including PPE gowning. The Manufacturing Technician I works collaboratively to support other manufacturing areas as required. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies for the role. | 11/29/2023 |
| 3607 | Masy Biosciences Morrisville, NC QC Data Review Specialist - Chemistry Master’s degree in Chemistry, Biology, or related field. Exp: 1+ years |
The Quality Control Data Review Specialist is an effective member of the Laboratory Operations team. Position is accountable for driving results in a fast-paced environment by effectively performing various activities at range of complexity to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data, conducting basic floor audits and process inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance-oriented training as necessary. The QC Data Review Specialist assists with the development of SOPs or other quality documents as needed. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. Business needs and deadlines will require employee to perform work duties outside of standard work hours on occasion. | 11/29/2023 |
| 3608 | Masy Biosciences Charleston, SC Pharmaceutical Manufacturing Technician - 2nd Shift Associate’s degree preferred. Exp: 1-2 years |
The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employs acceptable techniques while working in manufacturing environments, including PPE gowning. The Manufacturing Technician I works collaboratively to support other manufacturing areas as required. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies for the role. | 11/29/2023 |
| 3609 | Masy Biosciences Charleston, SC Pharmaceutical Manufacturing Technician - 3rd Shift Associate’s degree preferred. Exp: 1-2 years |
The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employs acceptable techniques while working in manufacturing environments, including PPE gowning. The Manufacturing Technician I works collaboratively to support other manufacturing areas as required. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies for the role. | 11/29/2023 |
| 3610 | Meridian Life Science Memphis, TN Lab Production Associate Bachelor’s or Master’s degree from an accredited institution with a relevant scientific discipline such as Chemistry, Biology, Biochemistry, Molecula Exp: 1+ years |
The Lab Production Associate position is responsible for performing assigned manufacturing and laboratory support activities according to company policies, SOPs, and quality regulations. The position will be responsible for performing upstream and downstream bioprocessing procedures to support the commercial manufacturing of native antigens, recombinant proteins, antibodies, and blockers. Upstream processes include tissue culture, cell bioreactors, fermentation, virus propagation, cell and virus bank production, and buffer/media preparation. Downstream unit operations include harvest, clarification, chromatography, centrifugation, TFF (UF/DF), filtration, formulation, and fill-finish. The candidate will be required to maintain an assigned lab area and perform equipment and lab cleaning procedures. The candidate must be able to execute assigned procedures in a fast-paced and results-oriented environment satisfying quality standards in accordance with customer satisfaction, cost, schedule, and ISO1345 regulations. | 11/30/2023 |
| 3611 | Meridian Life Science Memphis, TN Research Associate Bachelor’s degree from an accredited institution in a relevant scientific discipline such as Biology, Chemistry, Biochemistry, Molecular Biology etc. Exp: 1+ years |
The Research Associate will be responsible for providing hand-on support, within our Technical Operations and Development department, to drive the improvement and growth of our immunological reagent offerings including recombinant proteins, native antigens, antibodies, blockers, and custom manufacturing. The candidate will be expected to perform routine laboratory duties following company SOPs, protocols, and regulations. The role will assist with the execution of experiments under direct supervision of their supervisor performing experimental procedures, analytical procedures, analyzing data, and generating analysis reports. The candidate will be responsible for performing routine laboratory maintenance and lab management duties including maintaining sufficient supply of reagents, cleaning and disinfecting of laboratory equipment, cleaning lab area, environmental monitoring, and filling out proper paperwork. The candidate must be able to execute assigned procedures in a fast-paced and results-oriented environment satisfying quality standards in accordance with customer satisfaction, cost, schedule, and ISO13485 regulations. The Research Associate will be responsible for providing hand-on support, within our Technical Operations and Development department, to drive the improvement and growth of our immunological reagent offerings including recombinant proteins, native antigens, antibodies, blockers, and custom manufacturing. The candidate will be expected to perform routine laboratory duties following company SOPs, protocols, and regulations. The role will assist with the execution of experiments under direct supervision of their supervisor performing experimental procedures, analytical procedures, analyzing data, and generating analysis reports. The candidate will be responsible for performing routine laboratory maintenance and lab management duties including maintaining sufficient supply of reagents, cleaning and disinfecting of laboratory equipment, cleaning lab area, environmental monitoring, and filling out proper paperwork. The candidate must be able to execute assigned procedures in a fast-paced and results-oriented environment satisfying quality standards in accordance with customer satisfaction, cost, schedule, and ISO13485 regulations. | 11/30/2023 |
| 3612 | Myriad Genetics San Diego, CA Lab Tech II BS in Molecular Biology or related discipline. Exp: 1-2 years |
Execute high throughput preparations and dispenses of simple and complex reagents (enzyme formulations, primer combinations, large volume solutions) for our clinical lab using a variety of automated dispensing platforms; Assist in the receiving, handling, and monitoring of quantities and testing quality of raw materials and finished products; Assist in document manufacturing activities and quality control results; Auditing, stocking and equipment maintenance tasks | 11/30/2023 |
| 3613 | NAMSA Northwood, OH Microbiology Technologist Bachelor degree. Exp: no experience |
• May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. • Accurately collects and records raw data in logbooks and on worksheets. • May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. • May be required to perform required specific testing as applicable. • May be required to operate specified laboratory equipment. • May perform Environmental Monitoring, clean and disinfect cleanroom suites (required as applicable). • Other duties as assigned | 11/30/2023 |
| 3614 | NAMSA Northwood, OH LC-MS Chemist Master’s degree in chemistry or a related scientific field. Exp: no experience |
• Operates and maintains a variety of chromatographic and spectroscopic systems such as LC, LC/MS/MS, and GCMS to analyze biological and chemical elements as directed by assays or study protocols. • May order and/or stock supplies subject to approval. Maintain ancillary records (logbooks, worksheets). • Conduct routine studies independently according to work instructions. May be requested to conduct more involved studies. Routes all excursions or unusual testing occurrences to management. • Participate in the improvement of documents, test systems, quality systems, and workflow. | 11/30/2023 |
| 3615 | NAMSA Minneapolis, MN Laboratory Technician– Talent Pool An Associate or Bachelor degree in related scientific field is required. Exp: 1+ years |
• Conducts sample preparation for Sponsor materials as directed by study protocols for in vivo and in vitro biocompatibility assays and pharmacology, toxicology and analytical studies. • Performs the extraction process on prepared samples in accordance to ISO, USP and JMHLW regulations as directed by study protocols for biocompatibility assays. • Receives and logs Sponsor materials for testing. Completes chain of custody documentation for test article tracking. • Prepares and maintains sterile glassware for the sample preparation process. Processes glassware through washer, autoclave and depyrogenation oven as needed. • Operates, cleans and maintains incubators, autoclaves, hoods and other equipment routinely utilized. • Maintains an efficient and clean work area by organizing and restocking the sample preparation lab as needed. | 11/30/2023 |
| 3616 | NantKwest Culver City, CA Associate, Quality Control Bachelor’s degree in a life sciences discipline. Exp: 1+ years |
The Quality Control Associate in the Quality Control department is responsible for ensuring the timely execution of Quality Control Analytical assays in support of product release across all of ImmunityBio’s oncology and vaccine product platforms. This position will train on and perform a variety of molecular biology, and/or chemistry assays including but not limited to cell culture, ELISA, qPCR, HPLC, icIEF, CE-SDS techniques and/or Compendial test methods in the evaluation of product quality. | 11/30/2023 |
| 3617 | Nexelis Valencia, CA Laboratory Assistant Bachelor's degree in science preferred. Exp: 1+ years |
Process samples as required by each protocol. Assist laboratory technologists with sorting, processing, storage, and retrieval of medical specimens. | 12/1/2023 |
| 3618 | Nexelis Ithaca, NY Associate Scientist, LCMS (Sign on Bonus Offered) Bachelor’s Degree, Chemistry and/or Biology preferred. Exp: 1 year’s |
The Scientist Core LC/MS (Liquid Chromatography/Mass Spectrometry) employs liquid chromatographic separation techniques and mass spectrometric analysis for data collection. In addition to instrument operation, the Scientist LC/MS is responsible for some associated instrument maintenance, documentation in accordance with SOPs and regulations, and data processing in a manner which meets company quality best practices, objectives, and timelines. | 12/1/2023 |
| 3619 | Nexelis Ithaca, NY Associate Scientist Sample Preparation (Sign on bonus offered) Bachelor's Degree required. Exp: 1+ years |
Responsible for routine sample preparation duties inclusive of troubleshooting routine experiments, and the preparation of solutions and reagents. | 12/1/2023 |
| 3620 | Nexelis Ithaca, NY Associate Scientist Sample Preparation (Sign on bonus offered) Bachelor's Degree required. Exp: 1+ years |
Responsible for routine sample preparation duties inclusive of troubleshooting routine experiments, and the preparation of solutions and reagents. | 12/1/2023 |
| 3621 | Nexelis Indianapolis, IN Laboratory Assistant Bachelor's Degree Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree Required. Exp: 6 months |
Responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. | 12/1/2023 |
| 3622 | Nexelis Ithaca, NY Associate Scientist, LCMS (Sign on Bonus Offered) Bachelor’s Degree, Chemistry and/or Biology preferred. Exp: 1 year’s |
The Scientist Core LC/MS (Liquid Chromatography/Mass Spectrometry) employs liquid chromatographic separation techniques and mass spectrometric analysis for data collection. In addition to instrument operation, the Scientist LC/MS is responsible for some associated instrument maintenance, documentation in accordance with SOPs and regulations, and data processing in a manner which meets company quality best practices, objectives, and timelines. | 12/1/2023 |
| 3623 | Nexelis Austin, TX Laboratory Associate Associate degree Required or equivalent. Exp: 0–1-year |
Perform routine packaging and filling procedures with accuracy, consistency, and timeliness. Provide routine documentation and review of work performed in a timely manner. | 12/1/2023 |
| 3624 | Noble Life Sciences Sykesville, MD Research Technician Bachelor’s degree in biological sciences, biomedical engineering, or a related field. Exp: 1 year |
Description 1. Compliance: Perform assigned tasks and responsibilities under the direction of the Scientist(s) and/or the Study Director(s) and in accordance with relevant study protocols, regulations, and Standard Operating Procedures (SOPs). 2. Training: Ensure personal training is documented according to Noble SOPs prior to the performance of associated procedures. 3. Procedure Preparation: Label tubes and other supplies needed for collecting and processing specimens. Prepare reagents needed for collection or processing of specimens. 4. Performance of Procedures: Process various blood and tissue samples. Maintain quality, safety, and/or infection control standards. Perform procedures using various instrumentation according to Noble SOPs. 5. Documentation: Maintain lab notebooks and document experimental procedures and associated data. Assist in writing deviations and preparing responses to quality assurance audits related to duties performed. 6. Laboratory Maintenance: Take ownership of assigned laboratories. Coordinate with the inventory manager to stock assigned labs as needed. Maintain inventories of assigned cold storage units. Maintain the laboratories in a clean and organized manner. Prepare shipment packages as directed. 7. Collaborate: Collaborate with and assist other research technicians, research associates, study directors, study coordinators, and scientists across various departments. 8. Any other relevant duties as assigned. | 12/1/2023 |
| 3625 | Noble Life Sciences Sykesville, MD Jr. Research Associate Bachelor’s degree in biological sciences, biomedical engineering, or a related field. Exp: 1 year |
Ensure all necessary supplies needed to conduct the associated projects as specified by the protocols and/or SOPs are stocked. Print labels and label sample collection tubes and other laboratory reagents. Prepare data forms required to conduct the project as specified by the protocol and/or SOP. Assist in processing various blood and tissue samples. Assist in the preparation of samples using a variety of laboratory procedures for testing with various laboratory equipment. Conduct various laboratory procedures and operate analytical equipment. Maintain quality, safety, and/or infection control standards. Maintain the laboratories in a clean and organized manner after completion of procedures. Maintain lab notebooks and document experimental procedures and associated data. | 12/1/2023 |
| 3626 | Oakwood Labs Solon, OH Quality Control Chemist- Pharmaceuticals Bachelor's degree in Chemistry, Biochemistry, Biology, or related field. Exp: One to four years' |
We are adding to our Quality Control Chemistry Staff. We are currently seeking individuals to: Perform analytical testing of raw material, in-process product, final product release and stability testing. Clear documentation of test activities in approved worksheets and laboratory notebooks. Execute mathematical calculations as outlined in test methods. Assess data to determine if the material tested meets specifications. Peer review of quality control data. Participate in investigational testing and assist with root cause analysis. Create and review SOP’s and author Change Controls. Other general lab related duties as necessary | 12/1/2023 |
| 3627 | Oakwood Labs Oakwood Villiage, OH Chemist Bachelor’s degree in chemistry, biology, or related discipline. Exp: entry level |
Oakwood Laboratories is looking to add to their Analytical Chemistry Team! This is an excellent entry level opportunity for those interested in working at a technology-based pharmaceutical company. There will be on the job training rotations in the research and development lab and the quality control chemistry lab. You will gain hands-on experience analyzing and interpreting data for excipients, polymers, active ingredients, and finished pharmaceuticals utilizing advanced analytical instrumentation. You will work as part of small multi-disciplinary technical teams on both immediate and sustained release drug development projects in various stages of development including early proof of concept, supporting pharmacokinetic and clinical studies, technical transfer activities, and supporting commercial product manufacturing. You will have direct input on solving complex problems and contributing to project success. Become part of the Oakwood Labs team and advance your career with an industry leader in injectable pharmaceutical development | 12/1/2023 |
| 3628 | Pacific BioLabs Hercules, CA Microbiology Laboratory Analyst I/II An undergraduate or AA degree in a science-related field (e.g., Microbiology, Biological Sciences). Exp: 0-3+ years |
PBL has immediate openings for full or part time Microbiology Laboratory Analysts in the Microbiology Services Department. The Microbiology Laboratory Analyst will report to Microbiology Management and will contribute to general laboratory testing, sample management, and laboratory maintenance. The Microbiology Laboratory Analyst is expected to participate with the team to meet Microbiology Services Department goals and perform routine laboratory duties as directed. | 12/1/2023 |
| 3629 | Pacific BioLabs San Francisco Bay Area, CA Quality Assurance Specialist I Associate or B.S. in Chemistry, Biology, Microbiology, or equivalent experience required. Exp: 0-2 years |
Pacific BioLabs has immediate openings for full time Quality Assurance Specialist I in the Quality Assurance Department. The QA Specialist I will report to the Chief Quality Officer or designated individual. The Quality Assurance Specialist I is responsible for assisting management with the maintenance of the Quality Systems. The QA Specialist I must be sensitive to the demanding regulatory compliance requirements attending to the operation of a pharmaceutical testing laboratory. This job also requires the ability to demonstrate a high commitment to interpersonal relations. Work must be performed in compliance with Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), Quality System Regulations (QSR), ISO quality management system requirements, and other necessary regulatory requirements (e.g. OSHA, EPA, CDC, USDA, OLAW, etc.) as required by the task at hand, as well as any additional duties as assigned by the Chief Quality Officer. | 12/1/2023 |
| 3630 | Patheon Middleton, WI Entry Level Chemist Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 12/1/2023 |
| 3631 | Patheon St. Louis, MO Scientist I, Electrophoresis Analytical Development Bachelor in Molecular Biology / Chemistry / Biochemistry / Chemical Engineering, or a related field. Exp: no experience |
Responsible for developing or transferring analytical methods to support biopharmaceutical process development. You will work within an interdisciplinary team of scientists where you will learn and supply your skills and ideas to projects. | 12/1/2023 |
| 3632 | Patheon Cincinnati, OH R&D/Mfg Scientist I Associate’s or Bachelor’s degree in physical science; Chemistry or Biology preferred. Exp: 1+ years |
As a Laboratory Team Member, you will coordinate with your supervisor and collaborate with colleagues in diverse groups to assure that critical timelines are met. You will have the opportunity to collaborate with your peers within the laboratory and those in other departments such as formulations, operations, project management and quality assurance on a regular basis. You will perform analytical methods for elaborate testing for validated and experimental methods and other tests as needed to support lab operations. You will participate in the validation of analytical test methods when additional resources are required. | 12/1/2023 |
| 3633 | Patheon Cincinnati, OH Scientist I, Formulation & Process Development Minimum Bachelor of Science (BS) in science/engineering related field. Exp: 1+ years |
Supports execution for the development of new formulations and manufacturing processes of solids, liquids, and semi-solid dosage forms. Increase and develop knowledge regarding drug toxicology, pre-clinical – phase III, scale-up, and registration. Connect with technical leads, supervisors and project team peers (analytical and project management) on the progress and timely completion of activities and critical milestones. | 12/1/2023 |
| 3634 | Patheon Burlington, MA Labs FSP Associate Scientist - Raw Materials GMP Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1 year |
This position will work with others in Quality Control, Analytical Development teams, Quality Assurance, Manufacturing and CROs to support routine QC testing for Raw Materials for the manufacturing of Gene therapy products. The Analyst will specifically support the Raw material and gene therapy program pipeline (as needed) including but not limited to Project Management of the raw material program and development of testing strategies. | 12/1/2023 |
| 3635 | Patheon Middleton, WI Associate Scientist (Sunday -Thursday or Tuesday - Saturday) Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1+ years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 12/1/2023 |
| 3636 | Patheon Middleton, WI Associate Scientist - Mass Spec Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1+ years |
Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 12/1/2023 |
| 3637 | Charles River Laboratories Mattawan, MI Research Analyst I - Formulations 1 Bachelor’s/Master’s degree in a relevant field. Exp: no experience |
We are seeking a Research Analyst I for our Test Material Control/Formulations Department site located Mattawan, MI. A Research Analyst I - Test Material Control (TMC)/Formulations is responsible for: preparing, sampling, and dispensing formulated test material according to applicable Standard Operating Procedures (SOPs) and GxP guidelines. The individual in this role: completes projects on time while maintaining quality and efficiency; communicates effectively with management, internal customers, and team members; assists others with their duties; and may assist with troubleshooting formulation issues. The pay range for this position is $23.50/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. The shift is for the weekend, Friday to Monday 6 AM-2:30 PM but will train for the first 12 weeks Monday-Friday 6 AM-2:30 PM. When you work Saturday or Sunday there will be a 10% shift differential. | 11/20/2023 |
| 3638 | Charles River Laboratories Worcester, MA Research Technician I Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months |
We have an exciting opportunity for a Research Technician I (Tuesday through Saturday hours) at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. | 11/20/2023 |
| 3639 | Charles River Laboratories South San Francisco, CA Research Technician II - In Vitro B.S. or A.S. degree in a Life Science discipline, such as biology, veterinary science, or a related field. Exp: 1 - 2 years |
We are looking for a highly motivated Research Technician II - In Vitro (Rodent Facility) to join our Insourcing Solutions team located in South San Francisco, CA. | 11/20/2023 |
| 3640 | Charles River Laboratories Cleveland, OH Research Analyst I- Bioanalytical Bachelor’s degree (BA/BS). Exp: no experience |
We are seeking a Research Analyst I for our Bioanalytical Chemistry Team at our Safety Assessment site located in Cleveland, OH. Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP’s and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents. | 11/20/2023 |
| 3641 | Charles River Laboratories Mattawan, MI Research Analyst I - Bioanalytical 1 Bachelor’s degree (BA/BS). Exp: no experience |
We are seeking an experienced Research Analyst for our Safety Assessment site located in Mattawan, MI. Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP's and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents. | 11/20/2023 |
| 3642 | Charles River Laboratories Mattawan, MI Analytics Associate I Bachelor’s degree (Mathematics, Statistics, or Computer Science preferred). Exp: 0-2 or more years |
SALARY: The hourly rate for this position is $27.00. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. SCHEDULE: Monday - Friday, 8:00am - 4:30pm *flexible start and end time after 1-3 months of training We are seeking an experienced Analytics Associate for our Biostatistics Team at our Mattawan, MI site. An Analytics Associate is responsible for producing custom tables with statistical analyses using established systems and / or standardized code, to be completed in an accurate and timely manner consistent with the direction provided by the study director. | 11/20/2023 |
| 3643 | Charles River Laboratories Durham, NC Research Technician I Bachelor’s degree (B.A./B.S.) or equivalent in animal science or related discipline. Exp: 1+ years |
We are seeking a Research Technician I for our Discovery site located Durham. The following are responsibilities related to the Research Technician I: • Perform routine research activities as assigned, including in vivo-based screens. • Perform dosing of laboratory animals, animal husbandry. • Prepare & verify dosing solutions for administration. • Ensure that all individual study supplies are on-site & prepared in a timely manner. • Perform equipment maintenance. • Review protocol with manager to insure proper study execution. • Prepare & organize study data, study folders & data forms; perform data collection and entry. • Review study report, gives feedback on the accuracy of the materials & methods section; report data to more senior staff. | 11/20/2023 |
| 3644 | Hemacare Mattawan, MI Research Technician - Pharmacokinetics & Acute Toxicology 1 1 Bachelor’s/Master’s degree. Exp: no experience |
We are seeking an experienced Research Technician for our Pharmacokinetics & Acute Toxicology Team located in Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. | 11/20/2023 |
| 3645 | Hemacare San Diego, CA Husbandry Technician I B.S. in either animal science or life sciences preferred. Exp: one (1) year |
We are looking for a Husbandry Technician I (Rodent Facility) to join our Insourcing Solutions team located in San Diego, CA. | 11/20/2023 |
| 3646 | Hemacare Cambridge, MA Animal Support Technician I B.S. in Animal Science, Biology, or Biological Science. Exp: 6+ months’ |
We are seeking an Animal Support Technician to join our Insourcing Solutions team, located in Cambridge, MA. | 11/20/2023 |
| 3647 | Integra LifeSciences Plainsboro, NJ Manufacturing Engineer Bachelor's degree in Engineering (Mechanical Engineering, Pharmaceutical Engineering, Chemical Engineering, Biomedical Engineering). Exp: 0-2 years |
The Manufacturing Engineer will play a key role in the support of manufacturing operations, process scale–up, and manufacturing improvement activities. They will oversee projects to evaluate, analyze, and improve existing processes, support the development of new manufacturing processes, implement statistical process controls, analyze and trend existing process parameters, improve manufacturing yields, reduce scrap, and error proof manufacturing processes. | 11/21/2023 |
| 3648 | Integra LifeSciences Boston, MA QC Analyst I, Analytical - 2nd Shift Bachelor’s Degree in the biological or chemical sciences or equivalent. Exp: 1-3 years’ |
The QC Analyst I, Analytical – 2nd Shift, will be responsible for performing quality control Analytical laboratory testing of in-process, finished goods, validation studies, and adherence to all applicable regulations, policies, and procedures purchased components, manufactured sub-assemblies and final product. Must have working knowledge of U.S. Food and Drug Administration regulations, ISO 13485, and other applicable regulatory agencies as they pertain to laboratory testing. | 11/21/2023 |
| 3649 | MEDTOX Burlington, NC Research Associate I, Lab Automation Bachelor’s degree in chemistry, computer science, or an equivalent scientific discipline. Exp: 1+ years |
The Research Associate I-Lab Automation will be part of the Research and Development team that supports automation efforts in robotic liquid handling and data analysis. In this role, you will use mass spectrometry and other analytical technologies, provide assay development and validation support and assist in training and orientation of personnel as assigned. | 11/22/2023 |
| 3650 | MEDTOX Greenfield, IN Research Assistant I - Cell Based and Immunology Team BS/BA degree in science or related field. Exp: 1+ years |
Executes basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 11/22/2023 |
| 3651 | MEDTOX Greenfield, IN Research Assistant I BS/BA/BSc degree in science or related field. Exp: 1+ years |
Executes basic Molecular BioA (Mol BioA) laboratory procedures under the oversight of experienced personnel. | 11/22/2023 |
| 3652 | MEDTOX Greenfield, IN Research Assistant I-Protein Chemistry BS/BA degree in science or related field. Exp: 1+ years |
We have an excellent opportunity for someone to join our Protein Chemistry team in Greenfield, IN. In this role you will learn to execute basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 11/22/2023 |
| 3653 | MEDTOX Indianapolis, IN Analyst - BioAnalytical Lab, 2nd shift Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1+ years |
The Analyst is focused on the extraction of biological samples (Protein Preciptation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. Schedule: This is a 2nd shift position (2:00pm-10:30pm) scheduled Monday through Friday | 11/22/2023 |
| 3654 | MEDTOX Madison, WI Analyst Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1+ years |
The Analyst is focused on the extraction of biological samples (Protein Precipitation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. This position is a day shift with a flexible start time. | 11/22/2023 |
| 3655 | MEDTOX Madison, WI Research Lab Analyst Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1+ years |
The Analyst is focused on the extraction of biological samples (Protein Preciptation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. This position is a day shift with a flexible start time. | 11/22/2023 |
| 3656 | Merck West Point , PA B63 Associate Specialist, Engineering Bachelor’s Degree in Science or Engineering. Exp: 1+ years |
The Polysaccharide Vaccine (PV) Technical Operations team is seeking a highly motivated individual to fill an open position to support the start-up, process qualification, and successful licensure of new bulk vaccine manufacturing facility, Building 63, at West Point. The Associate Specialist, PV Technical Operations is responsible for technical support for bulk vaccine manufacturing unit operations while actively supporting, participating in, and embracing an empowered team culture. In this role, the Associate Specialist will work as an individual contributor as well as a team member within a cross-functional group that includes West Point Operations, Quality, Automation, Deviation Management, Global Technical Operations, Research and Development Division, and others. | 11/22/2023 |
| 3657 | Merck Elkton, VA Associate Manufacturing Science & Engineering Specialist Bachelor degree or higher in engineering, science, or business fields. New graduates or anticipated Fall 2023 graduates are also encouraged to apply. Exp: entry level |
At our Company's campus in Elkton, Virginia, we have an entry level position available to support and sustain our manufacturing processes. The manufacturing facility is located in the Shenandoah Valley along the Shenandoah River and the Blue Ridge Mountains a short distance from the University of Virginia and James Madison University. The successful candidate will have the opportunity to apply their enthusiasm and technical skills as a member of a multidisciplinary team supporting the operation of pharmaceutical, biopharmaceutical, and vaccine product manufacturing facilities. Depending on interests, education, experience, and skills, successful candidates will be matched with positions across the Elkton campus and may have the opportunity to participate in developmental rotations across functional areas. | 11/22/2023 |
| 3658 | Merck West Point , PA Off-Shift Specialist, Engineering Bachelor’s Degree in Science or Engineering. Exp: 1-3 years |
We are seeking a highly motivated individual to fill an open off-shift position to support the start-up, process qualification, and successful licensure of new bulk vaccine manufacturing facility, Building 63, at West Point. The Specialist, Operations is responsible for technical support for bulk vaccine manufacturing unit operations while actively supporting, participating in, and embracing an empowered team culture. In this role, the Specialist will work as an individual contributor as well as a team member within a cross-functional group that includes West Point Operations, Quality, Automation, Deviation Management, Global Technical Operations, MRL, and others. | 11/22/2023 |
| 3659 | Merck Rahway, NJ Specialist, Process Engineer - Oral Solid Dosage, Clinical Manufacturing Bachelor’s degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field. Master’s degree in Chemical Engineering, Ch Exp: BS: 1 year; MS: 0 years |
The Formulation, Laboratory, and Experimentation (FLEx) Center is a multi-modality (small molecule, biologics, vaccine) Drug Product development and Good Manufacturing Practice (GMP) clinical supply manufacturing facility in Rahway, New Jersey. The Process Engineer role at the Specialist level will serve as a leader in the FLEx Oral Solid Dosage GMP Clinical Manufacturing facility. This role will support formulation and process development, scale-up activities, quality investigations, change management and authoring GMP standard operating procedures and protocols in support of oral solid dosage clinical drug product operations. This individual will collaborate closely with the formulation scientists, engineers, quality representatives, and other team members to ensure the quality of the clinical supplies, the scientific rigor of the processes, and ultimately to enable the flexibility and speed of our Company's pipeline. The role is based in New Jersey and reports to the Oral Solid Dosage Process Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply. | 11/22/2023 |
| 3660 | Merck Kenilworth and Rahway, NJ Associate Scientist, Biologics Process Research & Development BS (or expected completion by May 2024) in Chemical/Biochemical/Biomedical Engineering, Biotechnology, Biochemistry, Microbiology, Structural biology, Exp: 1+ years |
In April 2020, our Company announced plans to consolidate our New Jersey campuses into a single New Jersey headquarters location in Rahway, NJ in 2023 and 2024. Therefore, this role will be temporarily based in Kenilworth and exact timing of the departmental move to Rahway, NJ will be communicated at a future date. Our Research Scientists are our Inventors. Using innovative thinking, state-of-the-art facilities, and robust scientific methodology, we partner to deliver the next medical breakthrough. Biologics Process Research & Development (BPR&D) within our company's Research Laboratories in our Research Division is on a mission to rapidly deliver diverse biotherapeutics to patients by efficiently developing innovative, robust manufacturing processes and technologies. To achieve this, we work closely with colleagues in Discovery, Pre-clinical, Early Development, Analytical, Formulation, and Commercial Manufacturing while providing a diverse and inclusive environment for all. Beyond process development for pipeline biologics, we innovate and build next generation biomanufacturing technologies. Examples include investments for development of continuous manufacturing, green and sustainable processes, and proprietary technology platforms. We actively publish and engage with the scientific community to influence the field. BPR&D includes three lab-facing technical functional areas: Process Cell Sciences (PCS), Upstream Process Development (UPD) and Downstream Process Development & Engineering (DPDE). This job posting covers opportunities for all three functional areas. We are actively looking for highly motivated people with a passion for innovation and interest in contributing to one or more of the three technical functional areas mentioned above. As an Associate Scientist in BPR&D you will work with a highly collaborative team of scientists and engineers to design, develop and execute robust processes in support of early- to late-stage biological products. You will apply rigorous scientific principles to solve challenging problems focused on developing the best processes to deliver life-changing medicines to patients worldwide. You will also have an opportunity to contribute to additional areas of interest such as biophysical, process, economic and/or multivariate modeling as we are committed to leveraging digital ways of working to enhance our ability to design robust processes. | 11/23/2023 |
| 3661 | PerkinElmer Annapolis, MD Chemical Media Buffer Technician Associate Degree in a chemistry, biology, or other relevant discipline. Exp: 1+ years |
Responsibilities: Perform FACS (Fluorescence-activated cell sorting) machine QC daily. Tasks include but are not limited to emptying sheath waste, refilling sheath tank and running daily test cycle. Perform preventative maintenance on the DNA sequencing machines. Task is performed 3 times weekly. Tasks include emptying and refilling buffer trays, rinsing and drying critical parts and contacting respective end-users with any issues or material orders. Check ViCell reagents and cups in all locations twice a week. Track levels of remaining ViCell reagents and cups and inform Lab Consumable Supplies when more needs to be ordered. Check volumes and fill Multitron and Stability chamber carboys 3x per week. (Mobile phase solutions for HPLC). Distribute distilled water for incubators daily. Deliver RODI (reverse osmosis deionized) and USP water to designated Labs. Distribute FBS from central stock to appropriate locations once per week; monitor central stock and track usage to inform when the reordering process needs to occur. | 11/24/2023 |
| 3662 | Sanofi Waltham, MA mRNA Senior Research Associate - Vaccine Bachelors in a related field (e.g., Cell Biology, molecular biology, biochemistry, etc.). Exp: 1-3 years |
As a part of the Discovery biology group at Sanofi's mRNA Center of Excellence (CoE), our team leads the development and implementation of high-throughput screening techniques to aid in the development of our next generation mRNA vaccines. Our team functions transversally and as such gets to work alongside all of the other R&D groups to achieve our goal of advancing our mRNA platform to the next generation. | 11/24/2023 |
| 3663 | Sanofi Framingham, MA Research Associate, Gene Therapy - Genomic Medicine Bioanalytics BS in biological sciences or related field. Exp: 1 – 3 years |
The Sanofi Genetic Medicine Unit CMC organization is responsible for the design and optimization of gene and cell therapy manufacturing processes and platforms. A key function of this group is to establish operational excellence in the manufacturing of Sanofi’s emerging portfolio of gene therapy products. The bioanalytical group provides analytical testing to support in process, release, and stability testing, as well as development activities for process optimization and life cycle management from early to late-stage clinical entry. The Research Associate is responsible for executing test methods under control of established procedures. Additional functions will include interpretation of data, preparation of test documentation, and management of analytical databases. We are looking for a candidate that is capable of learning quickly with the goal of executing analytical methods and managing assigned test schedules, with excellent communication skills. The position is primarily located in Framingham, MA but will be moving to Waltham, MA in Q4, 2022 | 11/24/2023 |
| 3664 | Sanofi Waltham, MA Senior Research Associate, Genomic Medicine Unit - Cell Culture Process Development Master’s degree in biological science or engineering discipline. Exp: 1+ years |
The Genomic Medicine Unit (GMU) CMC group at Sanofi is dedicated to the establishment of best in class manufacturing platforms to support development of life-changing advanced cell and gene therapy products, including recombinant AAV vectors, lentiviral vectors and cell therapy products. This organization encompasses vector and cell line engineering, upstream and downstream process development, analytics, and clinical manufacturing support. The cell culture process development group is responsible for viral vector production optimization and development of next generation production platforms to support high dose therapeutic products. The group is seeking a motivated Senior Research Associate to join the team | 11/24/2023 |
| 3665 | Sanofi Framingham, MA Senior Research Associate - QC, Genomic Medicine Bioanalytics - CT Master’s degree in Biology/Biochemistry or related discipline. Exp: 1+ years |
This position resides within the Genomic Medicine Unit (GMU), a part of Sanofi’s CMC Development organization. The GMU Analytical Development group has the overall responsibility to establish phase appropriate control strategies and to develop, qualify, and validate robust analytical methods to support release and characterization testing of different cell therapy candidates. The group supports cGMP-compliant in-process Quality Control (QC) support of cGMP Manufacturing cutting edge methods such as flow cytometry. The selected candidate will execute rapid turnaround cGMP testing of in-process materials. In addition, contribute to method improvement, qualification, and drug product testing prior to going to clinical trials. The candidate will work with the team to facilitate these goals. This group will be in Framingham working onsite. This position will be a rotating morning shift (9am-7pm), 4 days per week, and will be required to work two weekends a month | 11/24/2023 |
| 3666 | Sanofi Waltham, MA Senior Associate Scientist, Genome Engineering-NGS, Genomic Medicine Unit Master’s Degree. Exp: 1 year |
We are seeking a Sr. Associate Scientist to be part of a team focused on next generation sequencing in genome and cellular engineering in the Genomic Medicine Unit. The successful candidate will play a key supporting role in application of genome editing technology as an approach for treatment of cancer, rare blood and/or rare genetic diseases. | 11/24/2023 |
| 3667 | Sanofi Waltham, MA Senior Research Associate - Pilot Plant Operator Waltham, MassachusettsSenior Research Associate - Pilot Plant Operator Waltham, Massachusetts MS in a related discipline. Exp: 1+ years |
The gene therapy development and manufacturing group in Sanofi is responsible for the design and optimization of viral vector manufacturing processes and platforms. A key function of this group is to establish operational excellence in the manufacturing of gene therapy materials and products, through the development and implementation of robust and safe manufacturing practices, capable of supporting program needs, that are aligned with Sanofi internal standards and evolving regulatory expectations The manufacturing operations team is responsible for the safe and compliant execution of established manufacturing procedures to meet aggressive program deliverables. The team is responsible for “transfer-in” of manufacturing operations from development, as well as manufacturing of product to support internal program needs and external technology transfers for early and late-stage clinical gene therapy products. The Senior Research Associate will be responsible for executing upstream and operations under control of established manufacturing procedures and cross training of junior staff as needed. | 11/24/2023 |
| 3668 | Sanofi Framingham, MA Senior Manufacturing Technician Associate’s degree or Bachelor's degree. Exp: AS: 1-3 years; BS: 1-2 years |
This is a 12-hour, rotating position for within our Downstream Manufacturing team at our 8 NYA facility. 8 NYA is an integrated, continuous, biomanufacturing facility (ICBF). The facility is operated by Upstream, Downstream and Support Service groups which support a 24/7 large-scale therapeutic protein manufacturing facility housing multiple products. Initial job responsibilities will include supporting a diverse range of manufacturing related activities during plant start-up from Operational Commissioning/Shakedown through process validation (PV) and commercial operations. The Senior Manufacturing Technician will be responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMPs. | 11/24/2023 |
| 3669 | Invitrogen St. Louis, MO Scientist II, Process Development Master’s degree or foreign degree equivalent in Chemistry, Biology, Biochemistry, Chemical Engineering, or a related field of study. Exp: 1+ years |
DUTIES: Works with a variety of chromatography techniques including reverse phase, size exclusion, affinity, and ion exchange chromatography. Assists with the design of experimental plans based on defined deliverables. Conducts semi-routine and moderately complex tasks and sample analysis to support process development. Functions as a process subject matter expert in a cGMP environment. Assists with preparing protocols, reports, and test methods. Maintains and ensures safe laboratory environment and work practices. Executes, records, and evaluates experimental data appropriately, including the writing and revising of process development reports and technology transfer protocols as needed. | 11/24/2023 |
| 3670 | Invitrogen St. Louis, MO Scientist I, Electrophoresis Analytical Development Bachelor in Molecular Biology / Chemistry / Biochemistry / Chemical Engineering, or a related field. Exp: no experience |
Responsible for developing or transferring analytical methods to support biopharmaceutical process development. You will work within an interdisciplinary team of scientists where you will learn and supply your skills and ideas to projects. | 11/24/2023 |
| 3671 | Invitrogen St. Louis, MO Biopharmaceutical Production Technician II Bachelor’s degree in Biology, Biochemistry or Chemistry (or related) Exp: 1+ year |
The candidate will be responsible for the performance of operations in support of the manufacture of Commercial and Clinical Biologics. He/She will be responsible for following Current Good Manufacturing Practices (cGMPs) and carrying out a variety of functions related to Upstream (cell culture) and Downstream (purification) biopharmaceutical manufacturing. These functions may include but are not limited to activities such as propagation of mammalian cell culture, conducting aseptic cell culture operations, execution of large scare production bioreactors (50L - 2000L), conducting large scale chromatography, viral inactivation, viral filtration, ultrafiltration and diafiltration, as well as aseptic filling of bulk drug substance. | 11/24/2023 |
| 3672 | Invitrogen St. Louis, MO Formulation Technician I (Day Shift) Associates in a relevant scientific field or bachelor’s degree in Biology, Biochemistry or Chemistry preferred. Exp: AS: 1-3 years; BS: 0+ years |
The candidate will be responsible for the performance of operations in support of the manufacture of Commercial and Clinical Biologics. They will be responsible for following Current Good Manufacturing Practices (cGMPs) and carrying out a variety of functions related to Upstream (cell culture) and Downstream (purification) biopharmaceutical manufacturing. These functions may include but are not limited to activities such as propagation of mammalian cell culture, conducting aseptic cell culture operations, execution of large scare production bioreactors (50L - 2000L), conducting large scale chromatography, viral inactivation, viral filtration, ultrafiltration and diafiltration, as well as aseptic filling of bulk drug substance. We're currently hiring Biopharmaceutical Technicians and Buffer & Media Technicians on Day and Night shifts (12/hour shifts either 6:00AM-6:30PM or 6:00PM-6:30AM on a rotating schedule of a 2/2/3). Minimum base pay is $21/hour (plus built-in overtime). Base pay can vary per education, experience and position level. | 11/24/2023 |
| 3673 | Invitrogen St. Louis, MO QC Scientist I Bachelor’s degree in STEM field preferred. Exp: no experience |
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. | 11/24/2023 |
| 3674 | Invitrogen St. Louis, MO QC Scientist I - Environmental Monitoring Bachelor’s degree in STEM field preferred. Exp: no experience |
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale! Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. | 11/24/2023 |
| 3675 | Invitrogen St. Louis, MO Scientist I, QC Microbiology (4x10 Days; Wed - Sat) Bachelor’s degree required in a scientific field, preferably a Microbiology or Biology. Exp: 0 - 2 years |
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. | 11/24/2023 |
| 3676 | Jordi labs Mansfield, MA Senior Chemist 1 - Must be local to Mansfield, MA Masters of Science in Chemistry Exp: 1+ years |
Job Summary: Candidate will be responsible for Reports Preparation; preparing technical reports summarizing findings related to mass spectroscopy (LCMS, GCMS, PYMS) and chromatography methods (HPLC, GC), Designing Analyses; designing and implementing analytical strategies to help resolve complex, real world analytical problems including material failures, deformulations and quantitation, Performing Analysis; direct or perform mass spectroscopy or chromatographic analyses including overseeing method development and performing existing methods, Discussing Results; skilled at discussing analytical data and would be able to communicate in simple terms the results from a series of analytical tests. This would include helping other team members with interpretation as well as discussing results with customers. | 11/24/2023 |
| 3677 | Stryker Portage, MI Entry-level Electrical Design Engineer, R&D Bachelor's degree in Electrical Engineering or related discipline. Exp: 0+ years |
At Stryker we are dedicated to improving lives, with a passion for researching and developing new medical device products. As an engineer at Stryker, you will be proud of the work that you will be doing, using cutting-edge technologies to make healthcare better. Here, you will work in a supportive culture with other incredibly talented and intelligent people, creating industry-leading medical technology products. You will also have growth opportunities as we have a culture that supports your personal and professional development. | 11/13/2023 |
| 3678 | Acrotech Biopharma Dayton, NJ CHEMIST A BS/MS in a Scientific field. Exp: 1-3 years’ |
The Chemist will perform a variety of testing to assess the strength, identity and purity of finished product, which are mainly oral solids and/or raw materials. The Chemist will work as a member of a team to effectively plan and develop/validate new methods (for Assay, Dissolution, Residual solvents, and Related compounds tests) to execute analytical testing and/or test using established (official and/or in-house) test procedures. The Chemist may execute 90% - 100% of their work at the bench level. | 11/14/2023 |
| 3679 | Acrotech Biopharma Durham, NC ASSISTANT SCIENTIST BA/BS in Chemistry, Pharmaceutical Sciences or related field. Exp: 0+ years |
Capable of performing test methods for complex formulations under general oversight and documenting those experiments per cGMP requirements. Must be able to calculate, organize, and communicate results via standard data templates and reports. Experience in a cGMP laboratory and testing inhaled product (e.g. MDI and DPI) samples is preferred. Must possess good organizational skills, a commitment to quality work, and good oral and written communication skills, and work effectively as part of a team. | 11/14/2023 |
| 3680 | Acrotech Biopharma Dayton, NJ CHEMIST A BS with Chemistry is one of the subjects would be preferable. Exp: 1-3 years |
Chemist will perform a variety of QC testing to assess the strength, identity and purity of test samples and/or materials. The Chemist will work as a member of team to effectively plan and QC analytical testing using established (official and/or in-house) test procedures. The Chemist may execute 90% - 100% of their work at the bench level. | 11/14/2023 |
| 3681 | Repligen Auburn, MA Applications Engineer I Bachelor’s degree in engineering. Exp: 1-2 years |
Responsibilities Working closely with commercial team, convert customer conceptual design into a product solution that meets customer applications need Guide customer in selection of various raw materials that aligns with business preferred raw material Generate finish product cost estimates Product setup in ERP system which includes but not limited to creating Item Master, manufacturing router and Bill of materials. Initiate / Approve Engineering Change Orders for raw materials and finished products Travel required <10 % of time to visit industry events and customer visit | 11/14/2023 |
| 3682 | Cel-Sci Baltimore & Elkridge, MD Validation Technician B.S. in science or engineering or a related discipline or 2-year degree. Exp: BS: 0+ years; AS: 1 to 2+ years |
The Validation Technician is responsible for supporting validation activities of GMP equipment and systems. Assists in specifying and selecting equipment. Maintains all records related to qualification and validation. Prepares validation reports, suggests, and assists in determining specifications, and makes recommendations for modifications as necessary. The Validation Technician reports to the Validation Engineer. | 11/14/2023 |
| 3683 | Cel-Sci Baltimore & Elkridge, MD Validation Engineer B.S. in a related discipline. Exp: 1 to 5+ year |
The Validation Engineer is responsible for the regulation and support of equipment and systems. Assists in equipment selection, specification, and negotiating fees. Maintains all records related to qualification and validation. Works on projects where data analysis requires evaluation of defined factors to broad concepts. Utilizes independent judgment within broad parameters to determine an appropriate solution. Prepares validation reports, suggests and assists in determining specifications, and makes recommendations for modifications as necessary. The Validation Engineer reports to the Validation Supervisor. | 11/14/2023 |
| 3684 | Cel-Sci Elkridge, MD Manufacturing Process Technician BS/BA Degree in a related field or AA Degree in a related field. Exp: BS: 0+ years; AS: 1+ years |
The Manufacturing Process Technician contributes to the manufacturing team and participates in the manufacture of LI under GMP, and in process development and facilities operations and maintenance. The Manufacturing Process Technician reports directly to Supervisor of Manufacturing. | 11/14/2023 |
| 3685 | Cogent Professionals Indianapolis, IN Cellular Biologist/Biochemist BS - Biology, Cell/Molecular Biology, Biochemistry or related field or MS. Exp: 1-3 years |
We currently have a role available for a Cellular Biologist/Biochemist with industrial pharma experience. Job duties include, but are not limited to: Developing methods and assays, running assays efficiently, and recording and interpreting data. Strong cell culture (pre-clinical/mammalian) and aseptic technique skills needed. Ability to present data and summarize conclusions in written and oral forms. Utilizing Western blots, gel electrophoresis, MS and other biochemistry/molecular biology techniques. | 11/14/2023 |
| 3686 | Cogent Professionals San Diego, CA Entry-level Pharma Chemist BS-Chemistry or related field. Exp: 0-2 years |
We currently have a role available for an Entry-level Pharma Chemist. Job duties include, but are not limited to: Receiving and managing routine and daily orders. Weighing and preparing samples for storage and shipping. Sharing best practices and improvement opportunities. Working with laboratory automation (i.e. Hamilton, Tecan, etc.). Clearly documenting all laboratory duties. Keeping lab space clean and safe. | 11/14/2023 |
| 3687 | Cogent Professionals Pasadena, CA Molecular Biologist/Biochemist BS-Biology, Molecular/Cell Biology, Biochemistry, or related field. Exp: < 1 year |
We currently have a role available for a Molecular Biologist/Biochemist. Job duties include, but are not limited to, the following: Cell culture on a moderate scale and plating 96-well plates. Prepare reagents for automated liquid handling system. Preliminary analysis of data to verify completeness and accuracy. Some biochemistry background would be highly desirable, including Western Blot. Knowledge of liquid handling robots would be a plus (Tecan). Thorough documentation of experimental procedures via eLN (Benchling), reports, and technical documents. Compliance with all electronic notebook, safety, and quality SOPs is a must. Willingness to prepare and communicate technical presentations as needed. | 11/14/2023 |
| 3688 | Cogent Professionals Pasadena, CA Synthetic Chemist BS-Chemistry, Organic Chemistry, or related field or MS. Exp: BS: 1-3 years; MS: 0-1 years |
We currently have roles available for skilled Synthetic Chemists with industrial pharma lab experience. Job duties include, but are not limited to, the following: Synthesis of small molecules and proficiency in synthetic organic chemistry. Understanding standard unit operations (e.g., reaction set up, work up, flash column purification, isolation, and characterization), along with demonstrated technical problem-solving ability, is a must. Synthesis of peptides using automated peptide synthesizers and solution chemistry. Purification using preparative RP-HPLC, flash chromatography, FPLC, SEC, or equivalent. Bioconjugation of peptides/proteins using standard techniques. Strong expertise running and interpreting NMR, HPLC, and LC-MS data. Thorough documentation of experimental procedures via eLN, reports, and technical documents. Compliance with all electronic notebook, safety, and quality SOPs is a must. Willingness to prepare and communicate technical presentations as needed. | 11/14/2023 |
| 3689 | Debut Biotechnology San Diego, CA Research Associate - Downstream Process Development Bachelors/Masters degree in Chemistry, Chemical Engineering, or related subject. Exp: 0-2 years |
Debut Biotechnology is seeking a Research Associate in downstream process development for small molecule purification. You will assist in the development of robust & scalable downstream processes, and support pilot-scale process operations to maximize product yield. This individual should have familiarity with phenomena that can be leveraged for purification on a molecular level, as well as those that can be applied for physical material separations. As such, those with backgrounds in chemistry & chemical engineering are strongly encouraged to apply. Research Associate II and Senior Research Associate level candidates will also be considered. The successful candidate will work closely with the internal members of the downstream process development team, as well as the cross-functionally with fermentation scientists, pilot plant associates, biologists, chemists, and engineers. | 11/15/2023 |
| 3690 | Dicerna Pharmaceuticals Clayton, NC Filling Technician I - AP - Days AAS degree in a related field preferred. Exp: one (1) year |
The Position Filling of insulin & media preparations under aseptic conditions & operation of inspection equipment in order to achieve production goals | 11/16/2023 |
| 3691 | Dicerna Pharmaceuticals Clayton, NC Manufacturing Process Technician I - FP - NIGHTS AAS degree or military training preferred. Exp: six (6) months |
The Position Operate Assembly/Packaging manufacturing equipment in order to achieve production goals. | 11/16/2023 |
| 3692 | Dicerna Pharmaceuticals West Lebanon , NH Manufacturing Technician Bachelors’ Degree in a science discipline. Exp: zero (0) years’ |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. We offer both day and night shift positions (schedule below). With the growth of our site, we are seeking night shift suppport. Day Shift (7:00am-7:00pm) : Sun-Tuesday everyother Wedneday Thur-Saturday everyother Wednesday Night Shift (7:00pm-7:00am- includes 15% shift differential): Sunday-Tuesday everyother Saturday Wednesday-Friday everyother Saturday | 11/16/2023 |
| 3693 | Dicerna Pharmaceuticals West Lebanon , NH Manufacturing Technician - Night Shift Bachelors’ Degree in a science discipline. Exp: zero (0) years’ |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. With the growth of our site, we are seeking night shift support. We offer the following shift schedules that include a 15% shift differential: 7:00pm-7:00am (everyother week has 8-hours built in overtime): Sunday-Tuesday and everyother Saturday Wednesday-Friday and everyother Saturday | 11/16/2023 |
| 3694 | DxTerity Rancho Dominguez, CA Laboratory Technician/Scientist Molecular Biology, Lab Operations S. or M.S. in chemical, biological or clinical laboratory science, or medical technology from an accredited institution. Associate degree in a laborat Exp: 1-3 years |
Purpose of the Position: Testing biological specimens in molecular biology laboratory environment, including high throughput workflows, analyzing the results, and preparing them for reporting. | 11/17/2023 |
| 3695 | DxTerity Rancho Dominguez, CA Research Associate B.S. or M.S Degree in Biochemistry, Molecular Biology or a related field. Exp: 1-3 years |
DxTerity, a patient-centric genomics company located in Los Angeles, CA is looking to hire a Research Associate to join our Research and Product Development team. Responsibilities include: development of molecular diagnostic test kits, reagents and procedures in a team environment. Perform experiments independently after receiving general direction from supervisor. Make detailed observations, analyzes data and interpret results. Prepare technical reports, summaries, protocols and quantitative analyses. Maintain and develop skills in molecular biology and company technology through reading of internal reports and scientific literature. Support the achievement of project objectives and time schedules while meeting ISO and FDA regulatory and design control requirements. | 11/17/2023 |
| 3696 | Etubics Culver City, CA Associate, Quality Control Bachelor’s degree in a life sciences discipline. Exp: 1+ years |
The Quality Control Associate in the Quality Control department is responsible for ensuring the timely execution of Quality Control Analytical assays in support of product release across all of ImmunityBio’s oncology and vaccine product platforms. This position will train on and perform a variety of molecular biology, and/or chemistry assays including but not limited to cell culture, ELISA, qPCR, HPLC, icIEF, CE-SDS techniques and/or Compendial test methods in the evaluation of product quality. | 11/17/2023 |
| 3697 | Fluxergy Irvine, CA Manufacturing Engineer Bachelors or Masters degree in Mechanical Engineering or equivalent engineering degree. Exp: 1 to 3 years |
About the Role Are you a passionate and experienced Manufacturing Engineer ready to take on exciting challenges in the world of manufacturing and process engineering? Do you thrive in a dynamic, cross-functional environment where your skills can make a real impact? If so, we have the perfect opportunity for you! | 11/17/2023 |
| 3698 | Fluxergy Irvine, CA R&D Mechanical Engineer - Product Development Bachelor or master's in mechanical engineering, Biomedical Engineering, Bioengineering preferred. Exp: 1-4 years |
About the Role Would you enjoy taking the latest version of our flagship product from the design stage – all the way to a successful FDA 510K submittal - then commercialization? Does the idea of using your engineering skills to help decentralize traditional laboratory infrastructure sound like a cause you can get behind? If you answered ‘yes’ to both questions above, apply today! Your resume will be reviewed within days - everyone who applies will hear back from us. | 11/17/2023 |
| 3699 | Forbius Montreal, Quebec, CA Sample Manager and Biobank Coordinator Bachelor’s degree (B.Sc.) in Biochemistry, Cell Biology, Life Sciences or a related field. Exp: one (1) year |
We are currently looking for a multi-skilled Sample Manager and Biobank Coordinator to join our growing team in Montréal. In collaboration with our preclinical, translational and clinical teams, the incumbent will be in charge of sample management associated to our preclinical and clinical programs. | 11/17/2023 |
| 3700 | Free Think Technologies Branford, CT Analytical Scientist? Bachelor’s or master’s degree in chemistry, chemical engineering, or related scientific field. Exp: 0-6 years’ |
We are seeking a full-time Analytical Scientist to work in our laboratories in Branford, Connecticut. KEY RESPONSIBILITIES INCLUDE, BUT ARE NOT LIMITED TO Perform analytical measurements including HPLC/UPLC, GC, KF and dissolution testing Ensure all work performed complies with company standard operating procedures Develop and maintain technical expertise through continuing professional education and training | 11/17/2023 |
| 3701 | Fujifilm Diosynth College Station, TX Quality Control Cell Biology Analyst I Undergraduate degree in Biology or science related field; OR AAS in biology or science related field.Undergraduate degree in Biology or science relate Exp: BS: 0+ years; AAS: 1 year |
Summary The Cell Biologist I, under general direction, will be responsible for performing routine and non-routine quantitative and qualitative analysis of samples submitted to the Quality Control (QC) Laboratory. | 11/17/2023 |
| 3702 | Fujifilm Diosynth College Station, TX Quality Control - Microbiology Analyst I Bachelor of Science or Associate of Science degree preferably in Biochemistry, Chemistry, Biology or related field. Exp: 0+ years |
Summary: The Microbiology Analyst I will be responsible for assisting the QC microbiological aspects of cGMP compliance and testing at the FujiFilm Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory. | 11/17/2023 |
| 3703 | Haemonetics Clinton, PA Manufacturing Engineer Automation I Bachelor's Degree Engineering Exp: 0-2+ years |
This position is responsible to develop and implement changes to product design and/or to the manufacturing process to achieve significant quality, or cost improvements. Requires participation in new product development and existing programs, working with other business units to identify design-for-manufacturability issues and ensuring these issues are addressed prior to release.in a timely manner. | 11/17/2023 |
| 3704 | Haemonetics Clinton, PA Manufacturing Engineer I Bachelor's Degree Engineering; Master's Degree Engineering. Exp: 0-3+ years |
This position is responsible to develop and implement changes to product design and/or to the automation and manufacturing process to achieve significant quality, or cost improvements. Requires participation in new product development programs, working with other business units to identify design-for-manufacturability issues, ensuring these issues are addressed prior to release, and mentoring engineers. | 11/17/2023 |
| 3705 | Pace Analytical Lenexa, KS Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 11/17/2023 |
| 3706 | Pace Analytical Mt. Juliet, TN Scientist 1 - RadChem Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 11/17/2023 |
| 3707 | Pace Analytical Mt. Juliet, TN Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 11/17/2023 |
| 3708 | Pace Analytical Mt. Juliet, TN Environmental Scientist - Entry Level Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: Entry Level |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 11/17/2023 |
| 3709 | Pace Analytical Lenexa, CA Scientist 1 - Chemistry, Biochemistry Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 11/17/2023 |
| 3710 | Pace Analytical Mt. Juliet, TN Chemist (Scientist 1) Shift Differential Offered! Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 11/17/2023 |
| 3711 | Pace Analytical Ormond Beach, FL Chemist (Scientist 1) Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 11/17/2023 |
| 3712 | InVivo Biosystems Eugene, OR Lab Technician I - Zebrafish Husbandry Associates or Bachelor degree in Biology or related field preferred. Exp: one year |
This is a collaborative, team-based role with the responsibility to support transgenic and phenotyping client and grant-funded projects. On any given day you may perform zebrafish husbandry, general laboratory upkeep for zebrafish and c. elegans research. As you will be joining a growing biotech company, a passion for science, a positive outlook, and an ability to work in a dynamic environment are a must. | 11/17/2023 |
| 3713 | Ionetix Lansing, MI Mechanical Engineer (Lansing, MI) Bachelor’s degree in mechanical engineering. Exp: 1+ years |
Ionetix Corporation is seeking a Mechanical Engineer to design, develop, prototype, test and release mechanical and electromechanical designs of cyclotrons, automated chemistry systems, and related products. | 11/17/2023 |
| 3714 | Ionetix Sarasota, FL Site Production Technician (Sarasota, FL) A degree in a science field such as chemistry, microbiology, pharmaceutical, medical technology. Exp: 1+ years |
Ionetix is seeking a full-time Site Production Technician in Sarasota, Florida. This position will operate the cyclotron and purification unit to manufacture and release PET products, fully integrating the tracer production at the point of imaging. | 11/17/2023 |
| 3715 | Vigene Biosciences Rockville, MD Quality Control Associate - Environmental Monitoring B.S in Biology or related field. Exp: 1-2 years |
At Charles River Laboratories, we are looking for a highly motivated and energetic candidate to join our growing business in the CMO industry. The QC Analyst I will perform microbiological testing, static and dynamic viable and non-viable monitoring of classified clean room areas to support planned or in process manufacturing processes. This position, as well as all positions in the Charles River team will require demonstration of Charles River DNA “Characteristics and Behaviors” (Care, Lead, Own and Collaborate). | 11/17/2023 |
| 3716 | Boston Scientific Arden Hills, MN Quality Engineer I - Electrical Bachelor's degree or higher in Electrical Engineering. Exp: 1+ years |
The Electrophysiology (EP) Design Quality Assurance team is looking for an engineer to evaluate manufacturing and design changes. EP has a broad portfolio of capital equipment used in the field to support ablation and diagnostic procedures. The EP Design Quality assurance team is growing, and the timely evaluation of design changes is key to maintaining a robust EP Capital Equipment portfolio to reduce potential safety and quality issues. This role provides visibility across the Research and Design organization. The selected candidate will collaborate with Manufacturing, Product Complaints, Regulatory, and Field Servicing engineering. This is a significant role for an entry-level engineer with opportunities to grow into Computer Programming, Cybersecurity, Risk, or Electrical Design. The selected candidate will be mentored by a Senior Electrical Engineer. | 11/17/2023 |
| 3717 | BioPharmGuy Anywhere, US Contract Data Work some college Exp: 0 yrs |
We are looking for someone to help confirm mailing addresses in our directory. Mostly Googling. Can do work any time, any place. Must be able to accept payment via PayPal or Venmo. If interested, send a message through the contact form. Thanks! | 11/6/2023 |
| 3718 | Covance Greenfield, IN Research Assistant I - Cell Based and Immunology Team BS/BA degree in science or related field. Exp: 1+ years |
Executes basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 11/6/2023 |
| 3719 | Covance Greenfield, IN Research Assistant I - Protein Chemistry BS/BA degree in science or related field. Exp: 1+ years |
If you have a passion for science and working in a dynamic and fast paced lab with a cohesive team, the Research Assistant position will take you to the next level in your career. We have an excellent opportunity for someone to join our Protein Chemistry team in Greenfield, IN. In this role you will learn to execute basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 11/6/2023 |
| 3720 | Covance Greenfield, IN Research Assistant I BS/BA/BSc degree in science or related field. Exp: 1+ years |
Executes basic Molecular BioA (Mol BioA) laboratory procedures under the oversight of experienced personnel. | 11/6/2023 |
| 3721 | Covance Indianapolis, IN Research Assistant I BS/BA degree in science or related field. Exp: 1+ years |
Analyzes biological or chemical samples and/or develops/validates methodologies for various compounds and components in compliance with standard operating procedures (SOPs) and regulatory agency guidelines. | 11/6/2023 |
| 3722 | Covance Indianapolis, IN Analyst - BioAnalytical Lab, 2nd shift Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1+ years |
The Analyst is focused on the extraction of biological samples (Protein Preciptation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. Schedule: This is a 2nd shift position (2:00pm-10:30pm) scheduled Monday through Friday. | 11/6/2023 |
| 3723 | Covance Indianapolis, IN Research Assistant II Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1-2 years |
As a Research Assistant II in Bioanalytical Services you will be part of a cohesive team and conduct routine analysis on biological and chemical samples in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines for multiple studies. | 11/6/2023 |
| 3724 | Dexcom Mesa, AZ Process Engineer I Bachelor’s degree in a technical discipline. Exp: 0-2 years |
In this role, you will use sound and proven engineering principles to assist in designing and developing processes and requirements. The projects and activities will focus on Dexcom’s sensor technology. Working as a member of a technology team, you will collaborate with other engineers, management, and operators. This position will lead efforts to prove out manufacturing and automation processes to achieve design requirements specified by R&D, and explore and evaluate new technologies and concepts through analysis, prototyping, fixture design, and experimentation. This position will transfer and scale up new products from R&D. Involvement may begin from feasibility at vendors to full scale manufacturing. | 11/7/2023 |
| 3725 | Exact Sciences Madison, WI Clinical Laboratory Scientist - Tuesday - Friday, 8:00pm - 6:30am Bachelor's degree in a chemical, physical, biological or clinical laboratory science or medical technology from an accredited institution. Exp: 1+ years |
The Clinical Laboratory Scientist I performs laboratory analysis on clinical specimens using established laboratory procedures. The Clinical Laboratory Scientist I duties will include but are not limited to; processing of specimens, performance of moderate, and highly complex analytical testing, establishing, performing and documenting quality assurance, quality control, equipment maintenance, and accurately documenting all work performed under the direction of the Laboratory Medical Director. As a Clinical Laboratory Scientist I, you will recognize and resolve problems using good laboratory practices. Training: Monday - Friday, 7:00am - 3:30pm for the first 4 weeks Location: 650 Forward Drive and 145 E. Badger Road | 11/7/2023 |
| 3726 | ICON plc. San Antonio, TX Laboratory Assistant Bachelor’s degree (preferred). Exp: 1 year |
Duties: • Monitoring samples/Troubleshooting discrepancies. • Consolidating created samples/containers (i.e. slides, blocks, reports, etc.) • Searching and retrieving documents and samples. • Performing data entry/Monitoring e-mails and various correspondences. • Checking that slides/blocks are properly barcoded and labeled. • Assisting the pathologists with the technical/clerical work. | 11/7/2023 |
| 3727 | ICON plc. San Antonio, TX Laboratory Assistant Bachelor's degree (preferred). Exp: 1 year |
Duties: • Monitoring samples/Troubleshooting discrepancies. • Consolidating created samples/containers (i.e. slides, blocks, reports, etc.) • Searching and retrieving documents and samples. • Performing data entry/Monitoring e-mails and various correspondences. • Checking that slides/blocks are properly barcoded and labeled. • Assisting the pathologists with the technical/clerical work. | 11/7/2023 |
| 3728 | Eli Lilly Cambridge, MA Chemist/Sr Chemist - RNA Therapeutics BSc or MSc in Organic Chemistry or related field. Exp: 1+ years |
The successful candidate for this Chemist/Senior Chemist position will have a strong research track record in synthetic organic chemistry, be analytically minded, embrace data-driven decision making, and have experience in oligonucleotide chemistry and or bioconjugation. He/she will provide key technical knowledge and collaborate within a multidisciplinary team to support the development of next-generation RNA based therapeutics. | 11/8/2023 |
| 3729 | Eli Lilly Cambridge, MA Biologist - Cell Biologist Neurodegeneration BS and/or MS. Exp: 1+ Years |
The Cell Biologist position will be within the Proteostasis Group, which is part of the larger Neurodegeneration division. The primary responsibility will be culturing iPSC derived motor neurons as a cellular model of Amyotrophic Lateral Sclerosis to support the development of therapeutic agents. | 11/8/2023 |
| 3730 | Eli Lilly Cambridge, MA Biologist –Cell Biologist/Biochemist Neurodegeneration BS and/or MS. Exp: 1+ years |
The Cell Biologist/Biochemist position will be within the Proteostasis Group, which is part of the larger Neurodegeneration division. The primary responsibility of the role will be to develop and optimize cellular models of neurodegenerative disease as a platform for therapeutic development. The role will be focused on the biology of aggregate prone proteins such as TDP-43, synuclein or tau. | 11/8/2023 |
| 3731 | Eli Lilly Cambridge, MA Biologist –Biomarker Development Neurodegeneration BS and/or MS. Exp: 1+ years |
The Biomarker Development position will be within the Proteostasis Group, which is part of the larger Neurodegeneration division. In order to effectively diagnose and treat neurodegenerative diseases the identification and measurement of biomarkers is vital. The primary responsibility for this role will be the identification, development and optimization of assays which will support biomarker discovery for neurodegenerative disorders, such as ALS, Parkinson’s Disease and Alzheimer’s Disease. | 11/8/2023 |
| 3732 | Eli Lilly Indianapolis, IN Chemist- Nucleic Acid Synthesis Bachelor's and/or Master's degree. Exp: 1+ years |
The Lilly Genetic Medicines Team is looking for collaborative creative and energetic problem solvers to join a multidisciplinary team at the front edge of innovation. You will join our fast-paced, interdisciplinary team as we utilize novel RNA/oligonucleotide based therapeutic modalities to enhance the Lilly portfolio. The successful applicant will utilize their knowledge and technical expertise to complement and enable core capabilities and help drive the revelation and development of RNA-based clinical candidates. Do you have an aptitude for innovative approaches and modalities in discovery and development focused on identifying impactful therapies for the patient? We want you on our team! | 11/8/2023 |
| 3733 | Eli Lilly Pasadena, CA Chemist / Biochemist Undergraduate degree in chemistry, biochemistry, chemical engineering. Exp: 0+ years |
The team at Protomer is working on responsive biotherapeutics that can be controlled using small molecule modulators. Protomer team is based in Pasadena and the research labs are located in Pasadena. We are currently expanding the team to advance several programs, including glucose sensing insulins (GSIs), and are looking for a research associate with experience in biochemistry, synthesis, bioconjugations, and purification/characterization of therapeutic compounds of interest. The ideal candidate will have a bachelor’s or master’s degree in chemistry, chemical engineering, biochemistry, biology, or a related field, as well as in-depth understanding of basic biochemistry and chemistry techniques and experience with development, validation, and implementation of experiments in a biomedical research setting. The applicant must be a fast-learning, task-oriented, and self-motivated person who can perform detailed work with minimal supervision. A requirement of this role is to work well as a team player in a fast-paced research setting. The applicant will be responsible for assisting Protomer’s senior chemists with synthesis, bioconjugation, purification, and characterization of compounds of interest. The successful candidate will actively participate and present in team meetings and is expected to contribute to the team’s progress and success. | 11/8/2023 |
| 3734 | Eli Lilly Boston, MA Engineer, Downstream Process Development - Akouos M.S in Biochemistry, Chemical Engineering, Bioengineering or related discipline. Exp: 1+ years |
The Process Development group at Akouos is seeking an innovative Engineer to provide hands-on development support for the manufacturing of AAV-based gene therapy vectors. The ideal candidate for this position is an entry level Engineer with a background in AAV vector purification technologies and gene therapy downstream process development. The successful candidate will actively participate in downstream process development, scale-up, process optimization, and process tech transfer for GMP manufacturing. The successful candidate will thrive in a collaborative, scientifically stimulating, and fast-pace work environment. | 11/8/2023 |
| 3735 | Organogenesis Canton, MA Production Associate I-Collagen A Biotech certificate, Associate's degree, Bachelor's degree in Biology or a related science discipline is strongly preferred. Exp: 1+ years |
The Production Associate I - Collagen performs activities involved in the production of Collagen These activities include, but are not limited to, protein purifications, filtrations, and titrations in the production of high quality, purified, sterile collagen for both internal and external customers. This position requires working in a regulated area under the direct supervision of a team leader or departmental supervisor. | 11/8/2023 |
| 3736 | Organogenesis Canton, MA Production Associate I Bachelor’s degree or Biotech certificate. Exp: 1+ years |
The Production Associate will perform all activities involved in one of the following areas: the aseptic processing of a living product; the production of ICL and FortaFlex Products; or activities associated with HTP Product under the direct supervision the Manager. This role will support the Manufacturing Team by performing the tasks that will assure the safe and timely processing of our products, working in a Class 100/ISO 5, Class 10K/ ISO 7 and/or Class 100K/ISO 8 cleanroom. Sunday-Thursday schedule or Monday-Friday schedule, approximately 7:30am-4:00pm. Some weekend and holiday work required. | 11/8/2023 |
| 3737 | Meridian Medical Technologies Rocky Mount , NC MS&T Associate Process Engineer Bachelor’s degree. Exp: zero to one years |
As an Associate MS&T Engineer, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will make it easy to manage difficult issues and help in establishing consensus between teams. | 11/8/2023 |
| 3738 | Meridian Medical Technologies Rochester, MI Chemist / Microbiologist Master’s degree. Exp: 1+ years |
You will be a member of Pfizer’s dedicated and highly effective quality assurance and control team. You will be responsible for analyzing chemical, biological or microbiological products to support our quality programs. Your contribution to environmental testing, utility monitoring, analytical testing, microbial identification and sterility testing will help Pfizer provide safe drugs to patients. Your understanding of Quality Control instruments will help us meet their accuracy specifications against established standards. You will also be relied on for setting requirements for the transfer of methodology from R&D. As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate in explaining difficult issues and establishing consensus between teams. | 11/8/2023 |
| 3739 | Meridian Medical Technologies Andover, MA QC Technician (2nd Shift) Biotechnology Certificate/Associate Degree. Exp: 0-2 years |
You will be a member of Pfizer’s dedicated and highly effective Quality Control team. You will support commercial manufacturing and QC testing labs by managing sample lifecycle including bulk sample receipt, aliquot, labeling, delivery, and storage of QC test samples. Sample types may include release test, backups, retains, reference material, assay controls, and stability. You will support and maintain the retain program as required by CFR regulations. Monitoring of environmental chambers is also critical to the storage of the above sample types. Your contribution to the Quality Control Sample Operations team will help Pfizer provide safe drugs to patients. | 11/8/2023 |
| 3740 | Meridian Medical Technologies Rocky Mount , NC QC Chemistry Lab Analyst I Bachelor’s degree. Exp: 0+ years |
Your prior work experience and ability to apply your breadth of knowledge will help you adapt the standard methods and procedures. You will help us identify required delivery and process improvements that drive increased efficiency, throughput and quality. You will arrive at decisions on which methods and procedures are the best fit for different work situations. | 11/8/2023 |
| 3741 | Meridian Medical Technologies Rocky Mount , NC Manufacturing Quality Engineer- Quality Distribution Bachelor's Degree. Exp: 0 to 1 year |
You will be a member of Pfizer’s dedicated and highly effective quality assurance team. You will evaluate and review Pfizer’s clinical and commercial batches of drugs. You will make sure that product and process documents match the specifications based on established sampling and statistical process control procedures. Your expertise will help in identifying deviations from established standards, in the manufacturing and packaging of products. In the relevant cases you will approve investigations and change control activities to ensure compliance with configuration management policies. As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues. | 11/8/2023 |
| 3742 | Meridian Medical Technologies Kalamazoo, MI QC Laboratory Analyst II (1st Shift) Bachelor’s degree in Chemistry, Biochemistry or related science. Exp: 0-1 years |
You will be a member of Pfizer’s dedicated and highly effective quality assurance and control team. You will be responsible for analyzing chemical, biological or microbiological products to support our quality programs. You will also be relied on for setting requirements for the transfer of methodology from R&D. You will be developing and applying your knowledge of procedures, techniques, tools, materials and equipment. Your receptiveness to new ideas will enhance the team’s ability to achieve goals and targets. You will follow standard procedures to complete tasks and identify process issues or problems that involve direct application of your skills/knowledge. | 11/8/2023 |
| 3743 | Meridian Medical Technologies Sanford, NC QC Senior Associate Scientist - Method Transfer and Validation BS/BA Degree in Science/related field. Exp: 0 years |
You will be a member of Pfizer’s dedicated and highly effective Quality Control Team at Sanford, NC. Key responsibilities in QC Method Transfer and Validation (MTV) are performing tasks/activities associated with analytical method qualification, validation, verification and transfer. Specific activities include authoring/executing/review of protocols and reports associated with analytical method qualification/validation/transfer to support Pfizer’s quality programs. You will be responsible for participating in method transfer/validation activities to support Demo, Engineering, CTM (Clinical Trial Material), product/process validation and commercial batches manufactured at Pfizer. Additional responsibilities will include driving continuous improvement/Operational Excellence/innovative implementations and represent QC MTV on cross functional teams. Key responsibilities in this role include executing method transfer activities (verification, co-validation, validation, qualification) in the QC laboratory. Other responsibilities may include testing support, SOP revision, LIMS review etc. | 11/8/2023 |
| 3744 | Regeneron Tarrytown, NY Process Development Associate II, Analytics BS Exp: 0 – 2 years |
Regeneron's Preclinical Manufacturing & Process Development (PMPD) Analytics group is seeking a laboratory Scientist or Engineer interested in the analytical characterization of biopharmaceuticals. In this role, you will conduct analytical experiments that support manufacturing process development and research activities in a fast-paced laboratory setting. | 11/09/2023 |
| 3745 | Regeneron Tarrytown, NY Process Development Associate II, Cell Culture Development (PMPD) BS or MS in Chemical Engineering or Bio-related Engineering Exp: 0-3 years |
The Cell Culture Development Group within Preclinical Manufacturing and Process Development (PMPD) is looking for a motivated person to work as part of the medium and feed development team on projects for mammalian cell culture process medium optimization. In this role, you will perform studies at small scale to develop cell culture medium that improves cell growth, cell productivity, and/or product quality to support the extensive Regeneron clinical pipeline. | 11/09/2023 |
| 3746 | Regeneron Tarrytown, NY Sample Management Associate BS degree Exp: 0-4 years |
Regeneron’s Sample Management Group, located in Tarrytown, NY, is seeking a highly motivated Sample Management Associate to support biobanking operations and sample data processes. | 11/09/2023 |
| 3747 | Regeneron Tarrytown, NY Sample Management Associate BS degree Exp: 0-4 years |
Regeneron’s Sample Management Group, located in Tarrytown, NY, is seeking a highly motivated Sample Management Associate to support biobanking operations and sample data processes. | 11/09/2023 |
| 3748 | Regeneron Tarrytown, NY Sample Management Associate BS degree Exp: 0-4 years |
Regeneron’s Sample Management Group, located in Tarrytown, NY, is seeking a highly motivated Sample Management Associateto support biobanking operations and sample data processes. | 11/09/2023 |
| 3749 | Regeneron Tarrytown, NY Associate Scientist, Therapeutic Antibody Early Discovery BS or MS degree Exp: 0-5+ years |
Regeneron's Therapeutic Antibody Immunoscreening group is looking for a highly motivated Assoc Scientist to join our team. In this role you will contribute to the identification of potential therapeutic antibodies, in-vitro characterization and selection process of the lead molecules in early discovery stage. | 11/09/2023 |
| 3750 | Regeneron Tarrytown, NY Process Development Associate I, Bioreactor Development (1 of 3) Undergraduate degree. Exp: 0-3+ years |
Regeneron's Bioreactor Scale-Up and Development (BSD) team, a group within our Preclinical Mftg and Process Development (PMPD) organization, and which provides the link between small scale cell culture development and manufacturing, is seeking a Process Development Associate I. In this role you will assist the reagent productions to support pipeline and assay development needs for research groups and critical reagents to support GMP lot release. BSD performs cell culture up to 500 L scale and studies to support process transfer to manufacturing. | 11/09/2023 |
| 3751 | Steris Mentor, OH Quality Engineer Bachelor's Degree (In engineering or related technical field). Exp: 1-5 years |
The Quality Engineer is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. This role supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 11/09/2023 |
| 3752 | Steris Conroe, TX Quality Technician Associate's Degree in Engineering General or Science. Exp: (1) year |
The Quality Technician is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. The Quality Technician supports manufacturing and servicing operations by assisting in performing and documenting problem-solving investigations and conducting in-process sub-assembly and final QC product acceptance testing. Quality Technicians assist in identifying and documenting process and product non-conformances. They work with operations team members to perform and document problem-solving investigations. In addition, Quality Technicians may review device history records, authorize release of finished product/processes and execute calibration and environmental monitoring processes. | 11/09/2023 |
| 3753 | Steris Mentor, OH Mechanical Engineer Bachelors degree in Mechanical Engineering. Exp: one year |
The Mechanical Engineer will join a fast-paces Infection Prevention Technologies R&D team developing new Sterilizers. You will interact with other engineering disciplines and cross functional team member during the development lifecycle phases from concept development through final release. The mechanical engineering position will utilize problem solving techniques and engineering principals such as statics, machine design, thermodynamics, heat transfer, material selection and fabrication to develop solutions for medical equipment. You will be involved in 3D Modeling, Design Controls documentation, Design Verification Testing and hands-on prototyping while developing new and innovative solutions for our customers. *This position is located onsite in Mentor, Ohio with eligibility for a hybrid work schedule. | 11/09/2023 |
| 3754 | Steris Eden Prairie, MN Quality Engineer Bachelor's Degree in Engineering General or Science. Exp: 1-5 years |
The Quality Engineer is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. This role supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 11/09/2023 |
| 3755 | Steris St. Louis, MO Microbiologist Bachelor degree required, with a focus in Biology or Microbiology areas required. Exp: 0-5 years |
Are you interested in contributing to a healthier and safer world? The Associate Scientist (Microbiologist) is an entry level position that is responsible for supporting new product development through innovative research and through developing technical expertise in STERIS's Infection Prevention Technology product segments, including surface disinfectants and cleaners. The Associate Scientist, with the appropriate training and guidance, will work in the lab supporting the new product development team, operations and quality to enhance the sophistication and compliance of new, unique infection prevention solutions to meet the customer’s varying unmet needs. | 11/09/2023 |
| 3756 | Steris Arlington, VA Medical Equipment Integration Technician Associate's degree in Electronics, mechanical or similar degree. Exp: one year |
Are you mechanically and technology inclined with a knack for hands-on work and love to travel? Do you enjoy working independently and thrive in a fast-paced environment where you provide an exceptional customer experience? If you want to work for a great company where you will have the opportunity to advance your career, join our growing team as an Integration Technician specializing in installing Operating Room systems to integrate all equipment, audio/visual systems, and hardware and software solutions. ***This position requires overnight travel, up to 85% of the time, Monday - Friday*** This is a remote based customer facing position. To support and service our customers in this assigned territory candidates must be based out of one of the following states: Virginia. | 11/09/2023 |
| 3757 | Steris Montgomery, AL Quality Engineer Bachelor’s Degree (Engineering or related technical field). Exp: 1-5 years |
The Quality Engineer is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. This role supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 11/09/2023 |
| 3758 | BioDuro Irvine, CA Associate Scientist/Scientist, Analytical Development (Small Molecules) BS degree in Chemistry or related scientific discipline. Exp: 0-3 years’ |
The Associate Scientist/Scientist, Analytical Development independently performs analytical development activities and tasks to support formulation development and drug product manufacturing. The Associate Scientist/Scientist facilitates and assists in execution of systems to assure cGMP compliance for all relevant operations carried out within and for BioDuro, LLC. Responsible for performing advanced experiments and general laboratory duties. | 10/31/2023 |
| 3759 | BioDuro Irvine, CA Process Engineer BS degree in Engineering or Chemical Engineering preferred. Exp: 0-3 years’ |
The Process Engineer, under direct supervision, performs various duties related to optimization and analysis of production processes, new products, commercial process support and new product technology transfers. | 10/31/2023 |
| 3760 | BioDuro Irvine, CA Associate Scientist, Formulation Development BS in Chemistry or related field required. Exp: 1 year |
The Associate Scientist, Formulation Development, assists in the design and development of drug delivery systems and dosage forms. | 10/31/2023 |
| 3761 | Biomerics Salt Lake City, UT Process Engineer II Engineering Degree needed. Exp: 1-3 years |
The Process Engineer II will be responsible for supporting and improving the manufacturing of class II medical and surgical devices in a dynamic, customer-focused organization. You will be expected to work with customers to understand product and process specifications, develop manufacturing processes, and build and test devices to those specifications. All activities must be documented according to design control requirements in a design history file (DHF).P: The Process Engineer II may be an individual contributor in a small cross-functional team comprising engineering, operations, and quality members to provide process and manufacturability input to designs throughout the product development process. You will support verification, validation, and regulatory submissions of these devices, then lead the transfer of the products to production and ensure a smooth transition to the production engineering team. | 10/31/2023 |
| 3762 | Biomerics Winston-Salem, NC Manufacturing Engineer I or II Engineering degree. Exp: 0-5 years’ |
The ME will be expected to lead high-impact projects. The ME is expected to lead change, contribute new ideas, and find innovative methods to accomplish goals. Work with tooling/outside suppliers/in-house personnel performing analysis of situations or data and develop an in-depth evaluation of various factors. Acts independently and exercises judgment within broadly defined practices and policies. Determines methods and procedures for new assignments. The ME will be expected to have the ability to get things done through people who do not report to them. The ME will also need to have the ability to work through adverse situations while building and maintaining good personal relationships. | 10/31/2023 |
| 3763 | Biomerics Salt Lake City, UT Process Engineer II Engineering Degree needed. Exp: 1-3 years |
The Process Engineer II will be responsible for supporting and improving the manufacturing of class II medical and surgical devices in a dynamic, customer-focused organization. You will be expected to work with customers to understand product and process specifications, develop manufacturing processes, and build and test devices to those specifications. All activities must be documented according to design control requirements in a design history file (DHF). The Process Engineer II may be an individual contributor in a small cross-functional team comprising engineering, operations, and quality members to provide process and manufacturability input to designs throughout the product development process. You will support verification, validation, and regulatory submissions of these devices, then lead the transfer of the products to production and ensure a smooth transition to the production engineering team | 10/31/2023 |
| 3764 | Biomerics Salt Lake City, UT Lab Technician I - II Lab Technician I typically requires an associate or bachelor’s degree. Lab Technician II typically requires a bachelor’s degree in chemistry or a rela Exp: 1+ years |
Performs analytical and functional testing. Maintains glassware by picking up, cleaning, washing, sterilizing, and distributing. Keeps laboratory supplies ready by inventorying stock, placing orders, and verifying receipts. Keeps equipment operating by following operating instructions. Troubleshoots breakdowns maintains supplies, performs preventive maintenance, and calls for repairs—documents information by maintaining daily logs and equipment record books. Resolves problems by examining and evaluating data; select corrective steps. | 10/31/2023 |
| 3765 | PSC Biotech Remote Job, CSV Engineer I - Remote Job Bachelor’s degree in Computer Science, Engineering, or a related field. Exp: 1-3 years |
We are hiring motivated and passionate entry to junior level Computer Systems Validation Engineers to join our team. The successful candidate will have excellent communication and interpersonal skills, strong analytical and problem solving skills, and a strong drive to learn. While this is a remote position, candidates in Midwest and/or Pacific Time Zones are preferred. | 11/01/2023 |
| 3766 | PSC Biotech York, PA Manufacturing Associate I Associates Degree in Life Sciences/Liberal Arts field preferred. Exp: 1-3 years |
This position is responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMP/ISO requirement and standards as defined in FDA and EU applicable Regulations. With general supervision the individual will perform routine and critical manufacturing operations, including but not limited to work functions in aseptic and non-aseptic filling, equipment prep, cleaning dissolution and formulation activities. The individual may provide support in other departments within the company, including but not limited to, engineering, warehouse and facilities. The incumbent is also responsible and accountable for the execution of the PSC BioTechnique mission, “to maintain the integrity and professionalism of our products and services while enabling steady growth and development”. | 11/01/2023 |
| 3767 | Biotium Fremont, CA Chemistry Technician I (CHEMISTRY) B.S. or M.S. degree in Chemistry. Exp: 1+ years |
Under the direct supervision from a senior chemist, perform chemical purifications using chromatography including preparative HPLC or gravity chromatography; carry out chemical synthesis using standard protocols; carry out chemical analyses using modern instruments including analytical HPLC, LC-MS, TLC, UV/Vis and fluorescence spectrophotometry. | 11/02/2023 |
| 3768 | Biotium Fremont, CA Research Associate I, BIOSCIENCE B.S. or M.S. in Biology, Molecular Biology, Biochemistry or a related field. Exp: 1+ years |
Under supervision from Biotium scientists, perform biological testing of fluorescent dyes and related reagents. Perform production and quality control testing of assay kit components following standardized protocols. | 11/02/2023 |
| 3769 | Shape Therapeutics Seattle, WA Research Associate/Senior Research Associate, Research Technologies BS degree in Molecular Biology, Cellular Biology, Biochemistry, or a closely related field. Exp: one year |
ShapeTX is seeking a highly motivated Research Associate/Senior Research Associate (RA/SRA) to join our Research Technologies Team. This is an excellent opportunity for a motivated individual with demonstrated molecular biology expertise to contribute to the advancement of our RNAfixTM technology. In this multifaceted position, you will be at the forefront of developing innovative gene therapy payload designs for ShapeTX's disease programs, with responsibilities encompassing independent cloning of plasmids and constructs, employing techniques such as PCR, plasmid ligation, bacterial transformation, and DNA/RNA isolation. You will also play a pivotal role in evaluating novel payloads through tissue culture and transfection-based experiments while maintaining meticulous lab organization and communicating results effectively within our dynamic research environment. This role presents a unique chance to join the critical core of our Research Technologies Team within a rapidly growing biotechnology startup, offering substantial opportunities to contribute to groundbreaking biological applications addressing serious human diseases. | 11/02/2023 |
| 3770 | Shape Therapeutics Seattle, WA Research Associate/Senior Research Associate, AAV Purification - Cell, Assay, and Vector Engineering BS/MS in molecular/cellular biology or other relevant scientific discipline. Exp: 1-5 years |
ShapeTX is looking for a highly motivated individual with a strong passion for learning to join the growing Research team as Research Associate/Senior Research Associate, AAV Purification - Cell, Assay, and Vector Engineering. In this role, the successful candidate will purify and characterize AAV to support the early research pipeline and ShapeTX’s novel RNAfixTM and RNAskipTM technology platforms. The candidate will conduct exploratory research to develop novel AAV purification methods in addition to routine purifications. An ideal candidate will have demonstrated AAV/viral purification experience or broad recombinant protein purification experience a collaborative spirit, and a desire to work in a fast-paced startup environment. | 11/02/2023 |
| 3771 | Shape Therapeutics Seattle, WA Research Associate/Senior Research Associate, Virus Production and Engineering BS/MS in molecular/cellular biology or other relevant scientific discipline. Exp: 1/3 years |
ShapeTX is looking for a highly motivated individual with a strong passion for learning to join the growing Research team as a Research Associate/Senior Research Associate, Virus Production and Engineering. In this role, the successful candidate will generate AAV to support the early research pipeline and ShapeTX’s novel RNAfixTM and RNAskipTM technology platforms. An ideal candidate will have broad cell culture experience, an understanding of molecular biology techniques, a collaborative spirit, and a desire to work in a fast-paced startup environment. | 11/02/2023 |
| 3772 | Boston Analytical Salem, NH Quality Assurance Specialist I Bachelor’s degree in a related science discipline. Exp: 0-1 years |
The Quality Assurance Specialist supports the QA Lead and the company’s quality program by auditing chemists analytical data, routine work, protocols and reports. | 11/02/2023 |
| 3773 | Boston Analytical Salem, NH Analytical Chemist Bachelor’s degree in Chemistry or a related science discipline is required. Exp: 0-2 years |
The Analytical Chemist I conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. | 11/02/2023 |
| 3774 | Boston Analytical Salem, NH QC Microbiologist BA or BS degree in Microbiology or related science discipline. Exp: 0-2 years |
The QC Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 11/02/2023 |
| 3775 | Boston Analytical Salem, NH Microbiologist - Environmental Monitoring BA or BS degree in Microbiology or related science discipline. Exp: 0-2 years |
The EM Microbiologist conducts quantitative and qualitative analysis of pharmaceutical industries Environment according to FDA, ISO, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include Sampling of pharmaceutical industries through ISO standards and client specific test protocols. | 11/02/2023 |
| 3776 | Boston Analytical Framingham, MA Offsite EM Technician Associates degree preferred. Science classes or an associates degree in a scientific discipline is preferred. Exp: 0+ years |
The Offsite Environmental Monitoring Technician will perform Environmental Monitoring (EM) of pharmaceutical cleanrooms and the associated spaces on a daily basis according to FDA, cGMP and Boston Analytical's/Client Standard Operating Procedures. The position is primarily in the Framingham, MA area. | 11/02/2023 |
| 3777 | Boston Institute of Biotechnology Southborough, MA Research Associate - Downstream Process Development BS degrees in biology, biochemistry, biomedical/biochemical engineering, or related fields. Exp: ≤1 year |
A Research Associate I is an entry level position for Bachelor’s degree with no prior experience and reports to a scientist level or above on relevant projects. The individual is responsible for routinely setting up, operating, and maintaining the downstream lab equipment under direct supervision. | 11/03/2023 |
| 3778 | Boston Institute of Biotechnology Southborough, MA Research Associate - Upstream Process Development BS degree in Biochemical Engineering or related field of study. Exp: 0-2 years |
Responsibilities 1. Set up, execute, and monitor microbial and mammalian cell culture production in fermenters and bioreactors. 2. Collect, record, and report experimental data. 3. Provide updates to a team lead on a regular basis. 4. Maintain all notebooks and documentation according to department standards. 5. Write SOPs, and batch records. 6. Ability to work well in a team environment and independently as required. 7. Ensure and promote safe environmental and laboratory practices. 8. Order supplies as needed. 9. Prepare solutions and buffers. 10. Maintain lab space and equipment. | 11/03/2023 |
| 3779 | Boston Institute of Biotechnology Southborough, MA Research Associate - Analytical Development Bachelor’s or Master’s degree in Biology, Chemistry, Pharmaceutical Sciences, or a related/relevant discipline. Exp: Entry Level |
The Research Associate role within Analytical Development is an entry level position for individuals with a Bachelor’s or Master’s degree. Responsibilities include developing analytical methods for biologics characterization, characterizing samples from process development, and supporting subsequent clinical and/or commercial GMP manufacturing. | 11/03/2023 |
| 3780 | BostonGene Waltham, MA Research Associate, Molecular Biology & Next Generation Sequencing Bachelor’s (B.S.) degree in biology, clinical laboratory science, medical technology, or related discipline. Exp: 0-2 years |
BostonGene is seeking a highly motivated Research Associate to join our R&D team in our laboratory located in Waltham, MA. This candidate will support BostonGene’s state-of-the-art primary next-generation sequencing (NGS), adjunct analytical platforms, and automated analysis pipelines. The candidate will be expected to develop proficiencies in NGS support protocols, such as RNA and DNA isolation from tissue, cell-free DNA isolation from plasma, Whole Exome and RNA-Seq library preparation, qPCR, Molecular Biology techniques, and other sample QC techniques | 11/03/2023 |
| 3781 | Boundless Bio San Diego, CA Research Associate, HTS Screening, Drug Discovery BS/MS in biology related field. Exp: 1 year |
As a Research Associate at Boundless Bio, you will play a significant role in helping us transform exciting extrachromosomal DNA (ecDNA) discoveries into cancer medicines of the future. You will contribute to the process of developing robust, miniaturized high-throughput assays designed to enable drug discovery programs supporting multiple ecDNA-directed targets. This will involve broad application of biochemical and cellular assays across a range of formats to enable screening and SAR campaigns in support of our drug pipeline. These efforts will make an important contribution to the Boundless Bio drive for innovation in targeting difficult to treat cancers. | 11/03/2023 |
| 3782 | BPS Bioscience San Diego, CA Research Scientist I - Cell Biology M.S Exp: 1+ years |
BPS Bioscience Inc. is a leading provider of recombinant proteins, assay kits, lentiviruses, and recombinant cell lines for drug discovery. We are currently seeking a diligent and highly motivated scientist to join our cell biology group to assist in production and new product development. | 11/03/2023 |
| 3783 | BroadPharm San Diego, CA QC Chemist Bachelor or MS degree in Analytical Chemistry or Organic Chemistry is required. Exp: 1-4 years |
BroadPharm is a fast-growing biotech company which specializes in providing high purity PEG products and customer services worldwide. We are seeking a highly motivated QC Chemist to join our expanding team. The ideal candidate would already have 1+ year of working experience with HPLC, MS, and NMR. The position will work closely with the production team and regulatory manager in addition to the current QC staff. | 11/03/2023 |
| 3784 | Cabaletta Bio Philadelphia, PA Sr. Research Associate/Associate Scientist Molecular Biology M.S. degree in Life Sciences or closely related discipline. Exp: 1 -2 years |
Reporting to the Associate Director, Molecular Biology group, we are seeking an experienced and motivated Senior Research Associate or Associate Scientist. Under scientific and technical supervision, the candidate will design and produce molecular constructs that could be utilized for vector development and protein production. The individual will focus and work along for manufacturing small and large scale LVV gene therapy vectors across various preclinical programs and disease areas. The position offers growth into additional areas such as cell biology and molecular biology, immunology, and cell therapy. The position involves both technical and operational responsibilities. | 11/03/2023 |
| 3785 | Bayer Berkeley, CA Associate Electric Engineer M.S. Degree in Electrical Engineering or related discipline. Exp: 0-1 years |
Exciting and challenging electrical engineering opportunity where each day is different. Tasks would include evaluating electrical capacity, emergency power readiness, equipment maintenance, alternative sustainable energy solutions, and component electrical ratings analysis. Interact with cross-functions including Quality, Production, Procurement, Investment Management, Research and Development at the at the local, regional, and global levels as well as external vendors, and CA state supplier. | 11/03/2023 |
| 3786 | Bayer Pittsburgh, PA Manufacturing Associate II - O'Hara M-TH 5:30am-3:50pm Associate's Degree Exp: 1+ years |
This advanced position exists to provide experienced resources to assemble and support the various medical device manufacturing processes. It also provides a supporting role in the way of quality control in combination with advanced assembly, performed in a timely manner to meet quality and productivity goals of the department. This role will also assist the process coordinator or group lead in any training or cross training efforts as needed. The role will also interact between many departments to transmit information and recommend solutions to design, process and quality problems/non-problems. Leadership, a positive attitude and willingness to support teamwork is key! This role provides mentorship and support to the Manufacturing Production floor personnel in any way possible! This position will incorporate both Assembly and Quality inspections and requires more than one years’ experience at Bayer or in a position with related work experience | 11/03/2023 |
| 3787 | Bayer Luling, LA Chemical Production Engineer Bachelor’s of Science degree in Chemical Engineering, including May 2024 B.S. Chemical Engineering graduates. Exp: Up to 3 years |
The Chemical Production Engineer provides support to plan, coordinate, and execute technical activities needed to support manufacturing operations. Also, ensures the safe, efficient, productive, and environmentally sound manufacture of active ingredients or intermediates. | 11/03/2023 |
| 3788 | Bayer Berkeley, CA Associate Electrical Engineer M.S. Degree in Electrical Engineering or related discipline. Exp: 0-1 years |
Exciting and challenging electrical engineering opportunity where each day is different. Tasks would include evaluating electrical capacity, emergency power readiness, equipment maintenance, alternative sustainable energy solutions, and component electrical ratings analysis. Interact with cross-functions including Quality, Production, Procurement, Investment Management, Research and Development at the at the local, regional, and global levels as well as external vendors, and CA state supplier. | 11/03/2023 |
| 3789 | Abcam Waltham, MA Laboratory Technician - Proteins Associate's degree. Exp: one year |
Abcam is looking for a Lab Technician to join our team in Waltham MA, working to support the Protein Science team in the development of standalone recombinant products at Abcam. The goal of this product line is to deliver outstanding products to our customers and help Abcam achieve our aim of being the most influential company in life sciences by helping advance global understanding of biology and causes of disease, which, in turn, will drive new treatments and improved health. | 11/03/2023 |
| 3790 | Abcam Eugene, OR Research Associate - Biochemical Assay Design Bachelor's degree in Biochemistry, Chemistry, Biology, or a related field. Exp: 1+ years |
Abcam, a leading life sciences company, is seeking a motivated and detail-oriented individual to join our team as a Research Associate - Biochemical Assay Design in our Eugene, Oregon location. If you are passionate about advancing research in the life sciences and possess a strong background in biochemical assays, we encourage you to apply. | 11/03/2023 |
| 3791 | Agilent Carpinteria, CA Histology Laboratory Assistant Bachelors in biological sciences preferred. Exp: 1+ years |
The position will support the tissue procurement department and will include tasks and documentation to move new donor samples through incoming quality control to delivery of qualified samples to internal teams. This laboratory assistant position will have duties both in the lab and at the desk. | 11/03/2023 |
| 3792 | Bio Marin Pharmaceutical San Rafael, CA Research Associate (Temporary) Master’s degree in a scientific discipline or equivalent. Exp: 1 to 3 years |
We are searching for a talented and highly motivated Research Associate II to develop assay methods that will provide safety and efficacy data on experimental therapeutics entering clinical studies. The candidate will be responsible for the development of assays for diverse drug modalities, which may include gene therapies, monoclonal antibodies, oligonucleotides, biologics, and small molecules, with guidance from a Scientist in the Assay Strategy and Development group. The ideal candidate should have experience developing and optimizing bioanalytical methods, analyzing and interpreting experimental results, and communicating conclusions to other scientists. The successful candidate will participate in programs that range from exploratory in vitro and animal studies to non-clinical efficacy and safety studies and clinical trials. You will be responsible for developing new methods, evaluating novel technologies, conducting translational research internally at the BioMarin Research Center and externally in partnership with contract research organizations, and communicating results to cross-functional teams. This position offers a unique opportunity to interact with scientific and business colleagues across many functional areas, including Research, Translational Sciences, Regulatory Affairs, and Clinical Sciences. This RA II position will report to a Scientist in the Assay Strategy and Development group and will have the opportunity to advance our most promising pipeline programs to treat rare genetic diseases. | 11/03/2023 |
| 3793 | Bio Marin Pharmaceutical San Rafael, CA Research Associate II, Molecular Medicine, Translational Sciences Master’s degree in Biology, Chemistry, or like field. Exp: 0-2 yr |
The Molecular Medicine Group within the Translational Sciences Department at BioMarin Pharmaceutical is seeking a Research Associate II to help drive understanding of the underlying mechanisms for successful treatment with recombinant Adeno Associated Viral (rAAV) gene therapy and antisense oligo (ASO) modalities. The ideal candidate has a flexible mindset, natural curiosity and motivation to understand biology at the molecular and biochemical levels. The Molecular Medicine group aims to creatively apply the complete molecular and cellular toolkit to understand the contributing mechanisms of action or effect, in collaboration with colleagues across the company. We are positioned to help solve technically challenging questions that present as unexpected findings and/or have cross-program impact. We are currently particularly interested identifying early indicators and mechanisms that modulate the magnitude, durability and variability of expression of our gene therapy candidate(s). We work with cross-functional teams to develop and evaluate nucleotide integration capabilities for safety assessments. The Molecular Medicine group strives to improve technologies to enable analysis on small samples with definitive results, including at the single cell and nuclei level. The group collaborates with the entire set of Translational Sciences functions to understand the molecular and cellular actions of our therapeutics in preclinical experiments through clinical delivery to our patients. As our expanding clinical stage pipeline evolves, this RAII will have the opportunity to contribute to molecular investigations on a variety of therapeutic modalities and the genetic diseases that BioMarin strives to treat. This position will be primarily laboratory focused. The Research Associate II will be responsible for the design and execution of technically complex experiments to support multiple projects, with strategic input and guidance from Molecular Medicine and Translational Sciences leadership. S/he will provide quantitative data analysis, interpretation of results, and contribute to technical reports and scientific papers. S/he will evaluate existing complex methods and technologies, develop new solutions, and collaborate across functions to solve technical problems. The Molecular Medicine team values learning agility, open communication skills, willingness to support others’ experiments, and ability to trouble-shoot experiments on multiple platforms. The SRAII al | 11/03/2023 |
| 3794 | Bio Marin Pharmaceutical San Rafael, CA Research Associate II, Assay Strategy and Development (Temporary) Master’s degree in a scientific discipline or equivalent. Exp: 1 to 3 years |
We are searching for a talented and highly motivated Research Associate II to develop assay methods that will provide safety and efficacy data on experimental therapeutics entering clinical studies. The candidate will be responsible for the development of assays for diverse drug modalities, which may include gene therapies, monoclonal antibodies, oligonucleotides, biologics, and small molecules, with guidance from a Principal Scientist in the Assay Strategy and Development group. The ideal candidate should have experience developing and optimizing bioanalytical methods, analyzing and interpreting experimental results, and communicating conclusions to other scientists. The successful candidate will participate in programs that range from exploratory in vitro and animal studies to non-clinical efficacy and safety studies and clinical trials. You will be responsible for developing new methods, evaluating novel technologies, conducting translational research internally at the BioMarin Research Center and externally in partnership with contract research organizations, and communicating results to cross-functional teams. This position offers a unique opportunity to interact with scientific and business colleagues across many functional areas, including Research, Translational Sciences, Regulatory Affairs, and Clinical Sciences. This RA II position will report to a Principal Scientist in the Assay Strategy and Development group and will have the opportunity to advance our most promising pipeline programs to treat rare genetic diseases. | 11/03/2023 |
| 3795 | Bristol-Myers Squibb Phoenix, AZ Associate, QC Microbiology Operations Bachelor’s Degree in a scientific field preferred. Exp: 0-2 years’ |
2nd Shift- 2pm.-10:30pm. Position: EG 70-Associate, QC Microbiology Operations Location: Phoenix, AZ At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. | 11/03/2023 |
| 3796 | Bristol-Myers Squibb Devens , MA Manufacturing Associate II, Cell Therapy (12-hour shifts) Bachelors in relevant science or engineering discipline. Exp: 1+ years |
BMS Cell Therapy Manufacturing seeks an Associate II within Manufacturing that brings enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs. The candidate must be goal-oriented, flexible, and able to work efficiently with safety and quality in mind. We are searching for enthusiastic, and innovative individuals with a good understanding of good manufacturing practices to support routine manufacturing operations for Cell Therapy. | 11/03/2023 |
| 3797 | Bristol-Myers Squibb Devens , MA Bioprocess Associate (Night Shift) B.S., in science, engineering, biochemistry or related discipline, or its equivalent is desired but not required. Exp: 1+ years |
The Bioprocess Associate assists in the execution of commercial manufacturing processes according to established electronic work instructions and production records for the manufacture of therapeutic proteins in accordance with current Good Manufacturing Practices (cGMPs). *This is a rotating night shift position (5pm-5am), therefore eligible for a 20% shift differential. | 11/03/2023 |
| 3798 | Advanced Cell Diagnostics Minneapolis, MN Research Associate Bachelor’s degree. Exp: 0-2 years |
We are seeking an Research Associate for Bio-Techne’s Protein Purification department in Minneapolis. Our group supports 5000 different protein products used in academic research, pharmaceutical research, and all facets of biological science including: neurodegenerative diseases, stem cell research, glycobiology, developmental biology, etc. This individual will collaborate with many different departments to support the manufacturing processes of our products and contribute to the ongoing development of our growing and evolving portfolio. This position provides a potential for growth and career advancements within the company. This is a fantastic opportunity for an individual to gain problem solving and troubleshooting experience in a collaborative lab environment. This position also provides continuous learning and development, flexible working hours, and the ability to learn and apply a variety of lab techniques every day. | 10/23/2023 |
| 3799 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
We are seeking an Advanced Research Associate for Bio-Techne’s Protein Purification department in Minneapolis. Our group supports 5000 different protein products used in academic research, pharmaceutical research, and all facets of biological science including: neurodegenerative diseases, stem cell research, glycobiology, developmental biology, etc. This individual will collaborate with many different departments to support the manufacturing processes of our products and contribute to the ongoing development of our growing and evolving portfolio. This position provides a potential for growth and career advancements within the company. This is a fantastic opportunity for an individual to gain problem solving and troubleshooting experience in a collaborative lab environment. This position also provides continuous learning and development, flexible working hours, and the ability to learn and apply a variety of lab techniques every day. | 10/23/2023 |
| 3800 | Advanced Cell Diagnostics Minneapolis, MN RA - Advanced Research Associate Master’s degree. Exp: 1+ years |
Position Summary In this role, you would be responsible for the development and execution of QC test method validations for a variety of products, utilizing a wide variety of laboratory techniques. This position also assists in troubleshooting investigations and process improvement projects. As an Advanced Research Associate, you will also participate in cross-functional teams focused on new product introduction. | 10/23/2023 |
| 3801 | Advanced Cell Diagnostics Minneapolis, MN RA - Research Associate Bachelor’s degree in a related field. Exp: up to 3 years |
Position Summary: This position is responsible for participating in the development of Bio-Techne's various product lines. You will follow standard operating procedures to manufacture these products and will contribute to the ongoing development of new and existing products to help advance Bio-Techne's evolving portfolio. | 10/23/2023 |
| 3802 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate, Mammalian Cell Culture Bachelor’s degree in a biological science. Exp: 0 to 2 years |
POSITION SUMMARY This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for recombinant protein production, media and supplement preparation, and additional duties as assigned. This position requires a Sunday through Thursday workweek. | 10/23/2023 |
| 3803 | Advanced Cell Diagnostics Minneapolis, MN Research Associate - Protein Purification Development Bachelor’s degree in Biology or related field. Exp: up to 5 years |
Position Summary: We seek a highly motivated and creative individual to join our protein purification development team. Our team is responsible for the development of Bio-Techne's various product lines, with a focus on the high-quality recombinant protein products. You will participate in the development and optimization of protein purification procedures for recombinant proteins expressed in various cell lines (E. coli, baculovirus, and mammalian). In addition, you will also assist with initial, small-scale production for release of newly developed proteins and redevelopment of existing products to help advance Bio-Techne's evolving portfolio. This is a great opportunity to gain experience with cutting-edge biotech development/manufacturing processes & practices while working in a collaborative laboratory environment. | 10/23/2023 |
| 3804 | Advanced Cell Diagnostics Minneapolis, MN Research Associate, Analytical QC B.S. degree in Biochemistry, Chemistry, Biology, or a related field. Exp: 0 - 2 years |
Position Summary: As the Research Associate, Analytical Quality Control Analyst you will perform routine quality control testing of protein, peptide or antibody products using standard operating procedures to determine lot status, product release and product stability. Tests include concentration determination, SDS-PAGE with densitometry, endotoxin assay, PCR, HABA, conductivity, total organic carbon and other testing as assigned. Participation in the validation of new and existing laboratory methods is also expected. The position requires routine documentation, analysis, and communication of results within the department and across different groups. Other duties include instrument calibration and maintenance, record keeping, and lab support. Within this job function, the Research Associate must also pursue annual goals that aim to facilitate innovation, efficiency, productivity, and team building across the QC Department or the entire company. Perform additional duties as assigned. | 10/23/2023 |
| 3805 | Akouos Boston, MA Engineer, Downstream Process Development - Akouos M.S in Biochemistry, Chemical Engineering, Bioengineering or related discipline. Exp: 1+ years |
The Process Development group at Akouos is seeking an innovative Engineer to provide hands-on development support for the manufacturing of AAV-based gene therapy vectors. The ideal candidate for this position is an entry level Engineer with a background in AAV vector purification technologies and gene therapy downstream process development. The successful candidate will actively participate in downstream process development, scale-up, process optimization, and process tech transfer for GMP manufacturing. The successful candidate will thrive in a collaborative, scientifically stimulating, and fast-pace work environment. | 10/25/2023 |
| 3806 | Akouos Indianapolis, IN Chemist- Nucleic Acid Synthesis Bachelor's and/or Master's degree Exp: 1+ years |
The Lilly Genetic Medicines Team is looking for collaborative creative and energetic problem solvers to join a multidisciplinary team at the front edge of innovation. You will join our fast-paced, interdisciplinary team as we utilize novel RNA/oligonucleotide based therapeutic modalities to enhance the Lilly portfolio. The successful applicant will utilize their knowledge and technical expertise to complement and enable core capabilities and help drive the revelation and development of RNA-based clinical candidates. Do you have an aptitude for innovative approaches and modalities in discovery and development focused on identifying impactful therapies for the patient? We want you on our team! | 10/25/2023 |
| 3807 | Akouos Branchburg, NJ Engineer - Technical Services/Manufacturing Science BS degree in Chemistry, Microbiology, Biochemistry or related science, or BS in Chemical Engineering or related engineering discipline. Exp: 0-3 years |
This position is responsible for the technical support of manufacturing operations. This position will interact with the engineering, manufacturing, validation, quality assurance, quality control and regulatory departments. Interaction may be required with other Lilly site / contract producers of Lilly products. Knowledge of cell culture, purification and support systems used in the manufacturing of biotech products is required. Spreadsheet experience is required. Database experience a plus. | 10/25/2023 |
| 3808 | Alexion Pharmaceuticals Cambridge, MA Associate Scientist Masters Degree Exp: 1-2 years |
The Genomic Medicine group at Alexion Pharmaceuticals, AstraZeneca Rare Disease, has an outstanding opportunity for an Associate/Senior Associate position within the Genomic Medicine Group. We seek a highly motivated, curious, and detail-oriented individual with strong technical and problem-solving skills that would like to join our Rare Neurological and Rare Neuromuscular disorders team. The candidate will contribute to data generation, collaborate in discovering high-quality drug candidates, and will help build data packages to advance programs to IND. | 10/25/2023 |
| 3809 | Alexion Pharmaceuticals Cambridge, MA Senior Associate Scientist, Biology Master’s degree in Biology Exp: 1-2 years |
We are seeking a dedicated and innovative Senior Associate Scientist or Scientistto join our Genomic Medicine group at Alexion, AstraZeneca Rare Disease. The successful candidate will be a key member of the Alexion Genomic Medicine Cardiology team. The group’s mission is to discover and deliver transformational genomic medicines to patients with rare genetic cardiomyopathies. We are looking for a candidate with a background in cellular and molecular biology. In this role, you will be mainly responsible for developing and implementing a range of molecular and functional assays to assess the disease process, discover new medicines, and evaluate their therapeutic potential using human induced pluripotent stem cell derived cardiomyocytes (HiPSC-CMs). Additionally, you will be part of cross-functional teams and state of the art technology cores, and your scientific contributions will help advance Alexion’s preclinical programs to the clinic. | 10/25/2023 |
| 3810 | Alexion Pharmaceuticals Cambridge, MA Senior Associate Scientist, Biology Master’s degree in Biology Exp: 0-2 years |
We are seeking a dedicated and innovative Senior Associate Scientist to join our Genomic Medicine group at Alexion, AstraZeneca Rare Disease. The successful candidate will be a key member of the Alexion Genomic Medicine Cardiology team. The group’s mission is to discover and deliver transformational genomic medicines to patients with rare genetic cardiomyopathies. We are looking for a candidate with a background in molecular biology and experience with mammalian cell culture. In this role, you will be responsible for developing and performing molecular and immunoassays in samples collected from cells or mammalian in vivo models. With the support of cross-functional teams and state of the art technology cores, your scientific contributions will help advance our preclinical programs to the clinic. | 10/25/2023 |
| 3811 | Alexion Pharmaceuticals Cambridge, MA Senior Associate Scientist Master's Degree in cell biology and/or disease biology, pharmacology. Exp: 1-2 years |
We are searching for a dedicated and innovative Senior Associate Scientist to enhance our genomic medicine within Alexion, AstraZeneca Rare Disease. The chosen candidate will assume a pivotal role as a valuable member of the Alexion Genomic Medicine Cardiology team. Our mission revolves around pioneering genomic treatments for patients facing rare genetic cardiomyopathies. We are particularly interested in applicants with a robust background in pharmacology and disease biology. In this position, you will utilize your expertise in cardiac physiology to validate targets, plan and execute critical pre-clinical efficacy and safety studies, supporting the development of cardiac gene therapies from pre-clinical research to clinical development. You will collaborate closely with the biology lead, contributing preclinical in vivo data to ensure project timelines are met. | 10/25/2023 |
| 3812 | Alturas Analytics Moscow, ID Assistant Scientist Bachelor’s degree in a physical, biological or chemistry science required. Exp: 1-3 years |
The Assistant Scientist provides support to other laboratory personnel through a variety of duties and tasks. This is an entry-level position used to train all Associate Scientists. | 10/26/2023 |
| 3813 | Ampac Analytical Petersburg, VA Process Scientist III master's degree Exp: 0-3 years |
The Process Scientist is responsible for plant production support and the process development of pharmaceutical ingredients. Work is closely supervised. | 10/26/2023 |
| 3814 | Arbor Technologies Cambridge, MA Research Associate, In vivo Pharmacology, CNS MS degree Exp: 0-2 years |
The CNS Team at Arbor Biotechnologies is looking for a Research Associate interested in functioning at the cross section of technology and therapeutics. Our team is leveraging the strength of Arbor’s discovery platform to advance the cutting-edge CNS therapeutics utilizing in vitro and in vivo model systems. Arbor is a highly collaborative environment, and you will have the opportunity to work closely with the discovery, computation, and protein engineering teams, as well as to continue to explore new techniques for your professional growth. This role is at the forefront of Arbor’s translational evolution and will be given an opportunity to solidify the understanding of our assets for internal and external therapeutic development. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in an innovative company. Working at Arbor offers a unique opportunity that combines the fast pace and growth opportunities of a startup with the intellectual rigor and creativity of academia. A successful candidate in this position will be responsible for executing biodistribution and pharmacology/efficacy studies in mouse models of neurological/neuromuscular disease. You will also perform ex vivo tissue analyses from in vivo studies, including but not limited to tissue processing and molecular assessments. The ideal candidate will have direct experience in animal handling and dosing. | 10/26/2023 |
| 3815 | Arrowhead Pharmaceuticals Madison, WI Associate Scientist, Translational Biomarkers BS Exp: 1 year |
Arrowhead is seeking an Associate Scientist to join our growing Biology Department at our Madison site. This is an excellent opportunity to utilize, contribute and advance the ideal candidate’s laboratory skills in a progressive, state-of-the-art and diverse facility. | 10/27/2023 |
| 3816 | Arrowhead Pharmaceuticals San Diego, CA Associate Scientist, Bioconjugation B.S. or M.S. Chemistry or Biochemistry degree Exp: 0-8 years |
Arrowhead is seeking a highly motivated Associate Scientist to join our growing discovery chemistry team at our San Diego site. He/She will primarily focus on oligonucleotide bioconjugation, purification, analytical chemistry. As a siRNA chemistry bioconjugation specialist, you will play a pivotal role in the development and optimization of siRNA-based therapeutics by leveraging your expertise in bioconjugation strategies and siRNA chemistry. | 10/27/2023 |
| 3817 | Arrowhead Pharmaceuticals Madison, WI Associate Scientist, Small Scale Synthesis B.S. Chemistry or Biochemistry degree Exp: 0-2 years |
Arrowhead Pharmaceuticals is seeking an Associate Chemist to join the Discovery Chemistry Department. The successful candidate will primarily focus on oligonucleotide synthesis, purification, analytical chemistry, and contributing to specific program goals. S/He will be joining a team of highly motivated and experienced scientists and will contribute to the success of Arrowhead programs. | 10/27/2023 |
| 3818 | Ascent Pharmaceuticals Central Islip, NY Analytical Chemist Bachelor’s degree or foreign equivalent in Pharmacy/Chemistry or related field required. Exp: 1-2 years |
Ascent Pharmaceuticals, Inc. seeks Analytical Chemists for our Central Islip, NY location to develop, validate and conduct inter laboratory transfer of analytical methods for active pharmaceutical ingredients (API) and dosage forms; validate analytical methods and perform quality control activities; research & develop efficient and selective analytical procedures and draft/review laboratory SOPs; design, evaluate and monitor stability programs for drug products; work with advanced analytical equipment; supervise and train chemists and laboratory personnel; test drug substances, intermediates and raw materials while conducting impurity profiles for drug substances and intermediates; prepare ANDAs for FDA submissions etc. | 10/27/2023 |
| 3819 | Ascent Pharmaceuticals Central Islip, NY Quality Control Chemist Bachelor’s degree or foreign equivalent in Pharmacy/ Chemistry or related field required. Exp: 1-2 years |
Ascent Pharmaceuticals, Inc. seeks Quality Control Chemists in our Central Islip, NY location to collaborate with multiple departments including Manufacturing, Facilities, Engineering, Quality Control, Validation, Quality Assurance, and Regulatory to facilitate agreement on equipment, initiation and execution of Product development projects (ANDA Projects), process operational parameters, test requirements and acceptance criteria; Execute Change Controls to allow for the ongoing maintenance and optimization of validated systems and report KPI’s to higher management; Review and approve of a variety of validation lifecycle documents, project plans, user requirement specifications, SOPs, maintenance documentation, investigation reports, deviation resolution, CAPA closeout, etc.; Conduct internal & vendor audits in a group setting & under guidance from senior chemists/scientist for compliance with SOP, CGMP & FDA requirements. Research new regulatory guidance and cGMP and prepare reports for senior scientists and department heads to review and assist in drafting SOP’s; Critically evaluate current processes and continually identify ways to save time and money without sacrificing product quality; Investigate product, and process deviations, identify root cause, and develop corrective and preventative actions; Participate in audits by customers and regulatory agencies and respond to customer complaints in timely manner, review and close out market enquiries & investigations; Assist in APQR, Deviation & Investigation, Risk Assessment, CAPA Management, Change control management, Root Cause Investigation with SPC tools, Market Complaint Handling, Adverse event investigations; Review and Report Process Characterization Protocols, Equipment Qualifications, and review Process Validations of various ANDA drug projects; Conduct internal audits for compliance with SOP, cGMP & FDA requirements. | 10/27/2023 |
| 3820 | Ascent Pharmaceuticals Central Islip, NY Qiality Assurance Chemist Bachelor’s degree or foreign equivalent in Science/Chemistry or related field required. Exp: 1-2 years |
Ascent Pharmaceuticals, Inc. seeks Quality Control Chemists in our Central Islip, NY location to collaborate with multiple departments including Manufacturing, Facilities, Engineering, Quality Control, Validation, Quality Assurance, and Regulatory to facilitate agreement on equipment, initiation and execution of Product development projects (ANDA Projects), process operational parameters, test requirements and acceptance criteria; Execute Change Controls to allow for the ongoing maintenance and optimization of validated systems and report KPI’s to higher management; Review and approve of a variety of validation lifecycle documents, project plans, user requirement specifications, SOPs, maintenance documentation, investigation reports, deviation resolution, CAPA closeout, etc.; Conduct internal & vendor audits in a group setting & under guidance from senior chemists/scientist for compliance with SOP, CGMP & FDA requirements. Research new regulatory guidance and cGMP and prepare reports for senior scientists and department heads to review and assist in drafting SOP’s; Critically evaluate current processes and continually identify ways to save time and money without sacrificing product quality; Investigate product, and process deviations, identify root cause, and develop corrective and preventative actions; Participate in audits by customers and regulatory agencies and respond to customer complaints in timely manner, review and close out market enquiries & investigations; Assist in APQR, Deviation & Investigation, Risk Assessment, CAPA Management, Change control management, Root Cause Investigation with SPC tools, Market Complaint Handling, Adverse event investigations; Review and Report Process Characterization Protocols, Equipment Qualifications, and review Process Validations of various ANDA drug projects; Conduct internal audits for compliance with SOP, cGMP & FDA requirements. | 10/27/2023 |
| 3821 | Asha Pharma San Diego, CA SR./RESEARCH ASSOCIATE (SAN DIEGO, CA) BS/MS degree in Chemical Engineering, Materials Science, Chemistry, Pharmaceutical Science or related field. Exp: 0-2 years’ |
This position involves working in a laboratory that evaluates novel chemical compounds (typically pharmaceuticals) and discovers novel crystalline structures of the same as part of drug development. The Sr./Research Associate will independently work on projects related to crystallization R&D (e.g. polymorph, salt, cocrystal screening and crystallization process development for pharmaceutical and other molecules) under the guidance of a senior team member. The Sr./Research Associate will also help with Business Development Activities, providing a unique opportunity for well-rounded career development. | 10/27/2023 |
| 3822 | Astellas Westborough, MA Research Associate II, Analytical Development MS Exp: 0-2 years |
The Research Associate II will support assay development and qualification activities by performing cell culture and wet lab experiments, analyzing data, and drafting protocols, SOP’s and reports. This individual will be expected to execute protocols with some guidance and have the ability to summarize results independently. They will collaborate closely within the team and across functional groups to advance pipeline programs. | 10/27/2023 |
| 3823 | Astellas Westborough, MA Research Associate II, Analytical Development MS Exp: 0-2 years |
The Research Associate II will support assay development and qualification activities by performing cell culture and wet lab experiments, analyzing data, and drafting protocols, SOP’s and reports. This individual will be expected to execute protocols with some guidance and have the ability to summarize results independently. They will collaborate closely within the team and across functional groups to advance pipeline programs. | 10/27/2023 |
| 3824 | Astellas Westborough, MA Research Associate II, Analytical Development MS Exp: 0-2 years |
The Research Associate II will support assay development and qualification activities by performing cell culture and wet lab experiments, analyzing data, and drafting protocols, SOP’s and reports. This individual will be expected to execute protocols with some guidance and have the ability to summarize results independently. They will collaborate closely within the team and across functional groups to advance pipeline programs. | 10/27/2023 |
| 3825 | Astellas Westborough, MA QC Analyst I, Analytical B.S. degree in Biology/ or other life science related degree. Exp: 0-3 years |
Astellas, Westborough is seeking a highly motivated individual with strong organizational skills to join us as a QC Analyst I, Analytical. This position provides Quality Control compliance and testing support for Astellas cell therapy products. Looking for a strong GMP and scientific background and experience with quality control testing of cell therapies. | 10/27/2023 |
| 3826 | Astellas Seattle, WA Research Associate II, Stem Cell Therapies MS Exp: 0-2 years |
This Research Associate II position is a laboratory focused role with the primary purpose of providing support toward the development of novel stem cell derived cellular therapies. This position will work primarily in a laboratory setting with Scientists and R&D teams. | 10/27/2023 |
| 3827 | Astellas Seattle, WA Research Associate II, Core Technologies MS Degree Exp: 0-2 years |
We are seeking a highly capable, self-motivated Research Associate II for our Core Technologies Department . This individual will contribute to the molecular engineering for our gene edited Universal Donor Cells with activities focused on performing custom TaqMan based PCR assays. They will work as a key member on a fast-paced team to run molecular assays to characterize our proprietary Universal Donor Cells. | 10/27/2023 |
| 3828 | Astellas Sanford, NC Analyst II, QC Biochemical Operations M.S. degree in Biological Sciences Exp: 0-3+ years |
The Analyst II, QC will be responsible for implementing and executing analytical testing in support of clinical and commercial viral vector products in compliance with GMP requirements. Will also support testing for stability studies, methods validation studies and equipment validation. This position typically reports to the Manager, QC Biochemical Ops. | 10/27/2023 |
| 3829 | Aurora Biolabs San Diego, CA Research Associate I Bachelors or Masters in science related field. Exp: 0-1 year |
Aurora Biolabs, LLC is seeking a motivated research associate I in cell and molecular biology, biochemistry or related field in San Diego, CA. The individual will be a critical part of our products development team, development a new line of recombinant protein products for drug discovery and commercial use. This position requires extensive hands-on experience with a broad range of techniques including protein expression and purification, molecular cloning, PCR, mammalian cell, insect cells and bacterial culture, ELISA, as well as in vitro cell-based/immuno-based assays. You will work in an atmosphere that is stimulating, innovative, and customer focused. | 10/27/2023 |
| 3830 | Avedro San Clemente, CA Manufacturing Technician II - Glaukos bachelor’s degree in science or engineering Exp: 0 – 2 years’ |
The Manufacturing Technician II, based in San Clemente, CA, will perform all activities with good documentation practices (GDP) in accordance with current good manufacturing practices (cGMPs) and quality system regulation (QSR) medical device good manufacturing practices (GMP) requirements. | 10/27/2023 |
| 3831 | Azzur San Diego, CA Lab Technician II Associate’s or Bachelor's degree in Microbiology or related science. Exp: 1-2 years |
The LabTech II performs laboratory procedures related to Sample Receipt, Media Prep, Shipping and Receiving of Material, and Lab cleaning and maintenance. Lab Tech I has the responsibility to perform duties following established methods and protocols. | 10/27/2023 |
| 3832 | Azzur Schnecksville, PA Quality Specialist I Bachelor of Science or Bachelor of Arts in a science or engineering field. Exp: 1 - 3 years |
Azzur Labs is seeking a Quality Specialist I for their PA Laboratory. The Quality Specialist I supports the company’s quality assurance and control programs. The Quality Specialist I is responsible for document review and control, inventory control, and quality control of incoming materials. The Quality Specialist I will assist the Quality Manager in assuring that the quality management system is implemented and followed. | 10/27/2023 |
| 3833 | Azzur Devens, MA Quality Specialist I Bachelor of Science or Bachelor of Arts in a science field. Exp: 1-2 year |
Azzur Labs is seeking a Quality Specialist for their Boston Laboratory. The Quality Specialist I supports the company’s quality assurance and control programs. The Quality Specialist I is responsible for document review and control, inventory control, and quality control of incoming materials. The Quality Specialist I will assist the Quality Manager in assuring that the quality management system is implemented and followed. | 10/27/2023 |
| 3834 | Azzur Alameda, CA Quality Specialist I Bachelor of Science or Bachelor of Arts in a science or engineering field. Exp: 1 - 3 years |
Azzur Labs is seeking a Quality Specialist I for their CA Laboratory. The Quality Specialist I supports the company’s quality assurance and control programs. The Quality Specialist I is responsible for document review and control, inventory control, and quality control of incoming materials. The Quality Specialist I will assist the Quality Manager in assuring that the quality management system is implemented and followed. | 10/27/2023 |
| 3835 | Beam Therapeutics Research Triangle Park, NC Manufacturing Associate (Multiple Openings) BS, MS a plus, in Life Sciences or Engineering. Exp: 0-5 years |
Beam is expanding our geographical footprint to RTP, NC with the recent announcement of a 100,000 square foot manufacturing facility in addition to our laboratory-based facilities located in Cambridge, MA. We are looking for highly energetic Manufacturing Associates to support start-up and scaling of cGMP manufacturing at our new RTP site. The successful candidates will provide manufacturing, operational & technical experience around commissioning, training, qualification, and start-up. The ideal candidates will have experience in cell or gene therapy, along with demonstrated ability in a GMP environment. They will also possess the ability to successfully interface with multidisciplinary teams and build strong cross-functional relationships in a team environment. | 10/27/2023 |
| 3836 | Berkshire Sterile Manufacturing Lee, MA QC Analytical Associate I Bachelor’s Degree Exp: Zero to two (0-2) years |
The Quality Control Analytical Associate performs laboratory testing and administrative tasks for the QC department. Testing includes incoming materials, in-process samples, finished good and stability samples. It also includes performing experiments for method transfers, qualifications and validation. The QCA Analyst is responsible for creating and revising documents related to testing such as SOPs, test methods, protocols and reports. The position involves hands on activities such as laboratory testing, sampling of incoming materials, shipment of samples, inspection of samples and visual inspection of finished goods. | 10/27/2023 |
| 3837 | Berkshire Sterile Manufacturing Lee, MA QA Specialist Bachelor’s degree in scientific discipline, preferred. Exp: 1+ years |
Under general direction, the QA Specialist I is a quality professional who manages quality activities at BSM to meet cGMP and regulatory requirements at BSM. The QA Specialist I is responsible for maintaining and improving the Quality Culture at BSM. | 10/27/2023 |
| 3838 | Vor Biopharma Cambridge, MA Manufacturing Specialist I/II BS or MS in Biology, Biochemistry, Engineering, or related field. Exp: 1 - 5 years |
Vor Bio is seeking a Manufacturing Specialist I/II who is an enthusiastic and driven individual for cGMP manufacturing for early phase cell therapy manufacturing facility. The candidate will be responsible for providing support and executing in the manufacturing of Vor’s gene-edited cell therapies and maintaining compliance of cGMPs in manufacturing areas. | 10/16/2023 |
| 3839 | Voyager Therapeutics Cambridge, MA Sr. Research Associate, Vector Genome Master’s degree. Exp: 1-2 years |
Job Summary: Voyager Therapeutics seeks a highly motivated and experienced protein biochemist to contribute to its research team at its facility in Cambridge, Massachusetts. This is an ideal position for an individual with a background in protein biochemistry, who has a can-do attitude and strong work ethic, and thrives in a team-oriented, fast-paced, and cross-disciplinary biotech environment. As a Senior Research Associate on the team, you will be responsible for experimental execution and data analysis of various biophysical and biochemical assays to support pipeline programs and new research initiatives. | 10/16/2023 |
| 3840 | Walden Biosciences Cambridge, MA Associate/Research Associate, Cell Systems MS in molecular or cellular biology, or related field. Exp: 0+ years |
As an integral member of our Cell Systems team, the Associate/Research Associate will carry out laboratory research, working collaboratively with the Head of Cell Systems and other members of the Walden Team. This role will contribute to building out the group’s technical capabilities while concurrently undertaking experiments that further our drug discovery programs in vitro and in vivo translational models. | 10/16/2023 |
| 3841 | Zymo Research Tustin, CA Research Associate I BS or MS in Biology, Molecular Biology, Biochemistry, Genetics, or related field. Exp: 1+ years |
We are seeking a highly motivated and proactive individual to join our team for development of next-generation sequencing products as a Research Associate I. The successful candidate will work side by side with some of the most talented people in biotechnology across multiple teams and collaborative partners and will participate in independent product research efforts targeting the development of novel NGS workflows and reagents. The applicant will leverage their skills and familiarity with a range of molecular biology assays, as well as data analysis expertise, to efficiently manage a scientific research project and communicate and interpret data results effectively. The successful candidate will also be a quick learner, have a strong interest in science, and be passionate about a career in research. This position is a full-time and fully onsite role based in our Zymo Research facility in Tustin, CA. | 10/18/2023 |
| 3842 | Zymo Research Irvine, CA Bioinformatics Associate I Holds a master’s or bachelor's degree in Biology, Bioinformatics, Computer Science, Mathematics, Statistics, or a related discipline. Experience may s Exp: 1+ years |
Zymo Research is seeking a highly motivated individual to join our Microbiomics team! The qualified individual will play a key role in developing analysis pipelines for microbiome Next-Generation Sequencing data and performing cutting-edge data science to support Zymo Research’s global product strategy. As part of the Microbiomics team, you will leverage your skills and familiarity with NGS-based microbial sequencing methods in the research and development of new data analysis pipelines for our services, applications and exciting research projects! This position is fully onsite, full-time and is based at the Zymo Research Headquarters in Irvine, CA. | 10/18/2023 |
| 3843 | Zymo Research Irvine, CA Laboratory Technician Bachelor’s degree in Biology, Molecular Biology, Genetics, Microbiology, Biochemistry or related field is a plus. Exp: 1+ years |
Zymo Research is a leading biotechnology company committed to advancing genomics research and personalized medicine. We operate a state-of-the-art Next-Generation Sequencing (NGS) Service Lab, and we are currently seeking a dedicated and detail-oriented Laboratory Technician to join our dynamic team. As a Laboratory Technician in our NGS Service Lab, you will play a pivotal role in ensuring the seamless processing of samples, accurate nucleic acid isolation, precise library preparation, and efficient sequencing of genomic material. Your responsibilities will encompass a range of laboratory tasks, all critical to delivering high-quality results to our clients. If you are passionate about helping people in advancing science and working with awesome teams in a fast-growing company, we want you! This position is full – time, fully onsite and is based in the Zymo Research HQ location. | 10/18/2023 |
| 3844 | Accurus Biosciences Richmond, CA Research Associate Bachelor’s or Master’s degree in Biology Exp: 0-3 years |
JOB DESCRIPTION: The successful candidate will perform a range of duty critical to our research service business. The primary responsibility of this position is general molecular biology which includes DNA cloning, site directed gene mutagenesis, plasmid DNA preparation and DNA restriction analysis. Additional responsibilities for this position may include mammalian cell culture, protein transient production, stable cell line generation and general lab maintenance. | 10/19/2023 |
| 3845 | Sciecure Pharma Monmouth Junction, NJ QC & ARD Chemist Bachelor’s degree from four-year college or university in any of the following disciplines: Chemistry, Biology, Microbiology, or related sciences (as Exp: 1 year |
The Analytical R&D laboratory supports, development and validation of methods analytical test methods, evaluation and testing of raw materials, and testing of non-commercial materials to support product development. All activities are performed in accordance with specifications, standard operating procedures, approved test methods and/or protocols, regulatory requirements. | 10/20/2023 |
| 3846 | Sciecure Pharma Monmouth Junction, NJ Quality Assurance/Document Control Bachelor's degree in science or equivalent is required. Exp: Entry level |
Quality Assurance / Document Control position available at Sciecure Pharma Inc. We are seeking an entry level or partially experienced QA Associate on a permanent basis. Considering local candidates with GMP experience in a manufacturing setting within the QA department. | 10/20/2023 |
| 3847 | Sciecure Pharma Monmouth Junction, NJ Project Coordinator Bachelor’s degree in Life Science (Biology, Chemistry, Chemical Engineering, Etc.). Exp: 1 – 3 years |
Sciecure Pharma Inc. specializes in the research and development of pharmaceutical finished products from conception to commercial. Our growing company is seeking to hire a project coordinator who will be in charge of assisting in organizing our ongoing projects. This task involves monitoring project plans, schedules, organizing and participating in stakeholder meetings, and ensuring that project deadlines are met in a timely manner. To be successful as a project coordinator, you will need to be able to work on tight deadlines, be competent in using Microsoft Office applications such as Word and Excel, and have exceptional verbal, written, and presentation skills. A bachelor’s degree in life science is required for consideration. | 10/20/2023 |
| 3848 | AGC Biologics Boulder, CO Manufacturing Associate I-III BS in Chemistry, Biology or other relevant discipline. Exp: 1-7 years |
The Manufacturing Associate I-III performs GMP manufacturing operations safely, reliably and in compliance with stated processes. We offer a dynamic environment, innovation, operational excellence, and career growth. | 10/20/2023 |
| 3849 | AGC Biologics Seattle, WA QA Associate I-II, In Plant Operations BS degree in Biology, Chemistry or other relevant discipline preferred. Exp: QAAI: 0 - 2 years |
The QA Associate I-II, In Plant Operations is responsible for providing (24/7/365) Quality support to the activities listed below at the Bothell, WA site. Six (6) work shifts are active at the Bothell site: · This position will fill the night shift Wednesday-Saturday 2000-0630 | 10/20/2023 |
| 3850 | AKESOgen Peachtree Crossings, GA Clinical Lab Associate I - Accessioning Bachelor's Degree in a related field preferred. Exp: 0 or more years |
We are looking for a Clinical Lab Associate who will be responsible for Accessioning samples into our Laboratory Information Management System. | 10/20/2023 |
| 3851 | AKESOgen Peachtree Crossings, GA Molecular Technologist I-IV BS or MS in medical technology, clinical laboratory science, chemical, physical or biological science. Exp: 0-2 years |
Work in a cutting-edge clinical laboratory to provide high-quality molecular test data with rapid turnaround times. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Able to identify deviations from established SOPS and apply routine fixes for known and common issues with standard solutions under direct supervision. Perform molecular techniques, which might include quantitative PCR, next-generation sequencing, nucleic acid extraction, DNA/RNA quantification and qualification or genotyping. | 10/20/2023 |
| 3852 | AKESOgen Chicago, IL Molecular Technologist BS/MS in medical technology, clinical laboratory science, chemical, physical or biological science. Exp: 1 year |
Work in a cutting-edge clinical laboratory to provide high-quality molecular test data with rapid turnaround times. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform molecular techniques, which might include quantitative PCR, next-generation sequencing, nucleic acid extraction, DNA/RNA quantification and qualification, NGS library preparation, probe hybridization, probe/library capture, library cleanup and quantification, loading sequencing libraries onto the Illumina Nextseq, HiSeq4000, and Novaseq. | 10/20/2023 |
| 3853 | AKESOgen Chicago, IL Molecular Technologist I BS/MS in medical technology, clinical laboratory science, chemical, physical or biological science. Exp: 1 year |
Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Perform routine testing, quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures. Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols. Perform next-generation sequencing, including nucleic acid extraction, DNA/RNA quantification and qualification, NGS library preparation, probe hybridization, probe/library capture, library cleanup and quantification, loading sequencing libraries onto the Illumina Nextseq, HiSeq4000, and Novaseq. | 10/20/2023 |
| 3854 | Apton Biosystems Menlo Park, CA Scientist, Research Associate (Molecular) Bachelor's degree in Molecular Biology, Biochemistry or related field. Exp: 1 year |
Pacific Biosciences is looking for a Scientist, Research Associate (Molecular) who will serve as part of the product development team, contributing to the development of Single Molecule Sequencing products for the company’s real-time sequencing platforms. | 10/20/2023 |
| 3855 | Avidity Biosciences San Diego, CA Research Associate, Chemistry BS or MS in chemistry, biochemistry, chemical engineering, or related discipline. Exp: 0 – 3 years |
We are seeking a Research Associate, synthetic chemistry to join our team in La Jolla. This is a hands-on position with responsibility for the design, synthesis, and analysis of organic compounds. The ideal candidate will have biotech/pharma experience in aspects of medicinal chemistry, automated synthesis, and high throughput assay execution. The candidate is expected to be a strong team player, who enjoys scientific discovery and can communicate and collaborate in an interdisciplinary environment. | 10/20/2023 |
| 3856 | BioRestorative Therapies Melville, NY cGMP Bio -Manufacturing Engineer MSc degree in cell biology or similar discipline. Exp: 1 to 6 years |
BioRestorative Therapies, Melville, NY is recruiting for a cGMP bio-manufacturing engineer. This role provides outstanding opportunities for talented self-motivated individuals, ideally with experience in (stem) cell biology, immunology, and/or molecular biology, who can contribute to our ongoing efforts to generate clinical grade cell-based therapeutics. We are most interested in connecting with qualified individuals who aspire to support the development of therapeutics and/or life science products and tools to support research endeavors. | 10/20/2023 |
| 3857 | ChemPacific Baltimore, MD Chemist Master’s degree in Chemistry or Organic Chemistry. Exp: one year |
Perform multi-step organic synthesis in solution and/or solid support: Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps such as extraction, recrystallization, silica gel column chromatography and LC/MS purification; perform cGMP synthesis of pharmaceutical ingredients; and perform process development and scale-up for kilogram quantities; and clearly record and communicate results and challenges to coworkers/supervisor. Equipments and tolls used included NMR, UV, MS and IR, Reactor (from 50ml to 221 to 10000l), vacuum pump, water aspirator, condenser, rotavap, voltage transformer, chromatography columns, TLC monitor, lyophilizer, separation funnel and addition funnel. Please send your resume to xtan@chempacific.com | 10/20/2023 |
| 3858 | CRISPR Therapeutics San Francisco, CA Research Associate II, CRISPR-X MS in biology or related disciple. Exp: 0-2 years |
We are seeking a Research Associate II to join the CRISPR X group at CRISPR Therapeutics, the leading gene editing company. The successful candidate will be an integral part of a team whose aim is to advance next generation gene editing. The position requires enthusiasm, passion, attention to detail and a desire to assist in developing the next generation of gene editing. | 10/20/2023 |
| 3859 | IDbyDNA San Diego, CA Scientist 1 Scientist 1 Bachelor’s degree. Exp: 0-2 years |
Position Responsibilities: · Executes planned experiments/analysis of moderate to advanced complexity within immediate team and performs routine chemical and biochemical testing; uses insights to help troubleshoot problems · Contributes ideas for meeting project goals and invention disclosures · Assembles data for analysis using accepted methods and distills key conclusions while keeping an organized laboratory notebook and implementing protocols · Provides supporting data to Project Lead on risks in area of responsibility · Understands internal customers and collaborators and their needs and expectations · May train internal customers in areas of expertise Listed responsibilities are an essential, but not exhaustive list, of the usual duties associated with the position. Changes to individual responsibilities may occur due to business needs. | 10/20/2023 |
| 3860 | IDbyDNA San Diego, CA Engineer 1 - Mechanical Design (R&D/Precision Motion) BSc/MS in ME, EE, Mechatronics, Robotics OR related background. Exp: 0-2+ years |
Responsibilities: Design and test of high precision motion stages Successfully transition designs from concept to production Assist in test development, including nanometer level metrology Analyze designs for vibration and optimal performance and stability Work on teams to perform root cause analysis and methodically solve problems Communicate clearly with team members and leaders Manage and coordinate with external suppliers and manufacturers | 10/20/2023 |
| 3861 | Lampire Biological Labs Coopersburg, PA Abattoir Technician College degree a plus. Exp: 1-2 years |
Job Description: The Abattoir Technician is responsible for collecting, processing, and packaging animal blood and/or tissues sourced from abattoirs. This role involves meticulous attention to detail, adherence to safety and quality standards, and the ability to work at both our laboratory and off-site abattoir/vendor locations as necessary to meet production needs. | 10/20/2023 |
| 3862 | Lampire Biological Labs Pipersville, PA Laboratory Animal Technician Bachelor's Degree in a scientific field preferred. Exp: 0-2 years |
Scope of Responsibility: The project related functions for the small lab animals, including but not limited to mice, rats, guinea pigs, and hamsters. This person will be responsible for preparing and administering injections, performing bleeds, processing bleeds and updating records as needed. To perform animal procedures as the project dictates on small laboratory animals and input data at Lampire with the goal of providing consistent, high quality products and services to our customers with complete, accurate documentation. | 10/20/2023 |
| 3863 | Pharma Tech Industries Royston, GA Quality Control Analytical Chemist I BS degree in Chemistry or BS degree in Biology. Exp: 0-3 years’ |
Pharma Tech Industries (PTI Royston, LLC) is seeking to hire a Quality Control Analytical Chemist I for the Royston, GA facility. Primary responsibilities include performing all duties necessary as a QC Analytical Chemist under the general direction of the department supervisor. This position will report directly to the Quality Laboratory Manager. | 10/20/2023 |
| 3864 | PL Developments Lynwood, CA Chemist III BS in Chemistry / Biochemistry. Exp: 1+ years |
Perform analysis in the functional areas of analytical testing using modern analytical equipment such as HPLC, FTIR, UV, GC, ICP, as well as Wet Chemistry using titration techniques. Provide analytical testing in support of production, analyzes Raw Material, In-Process, Finished product, Stability samples and investigation samples and analyzes and interprets the test data and document result in a timely manner. Thorough understanding and compliance with FDA cGMPs / cGLPs / USP / ICH / SOPs / Test Methods and other recognized standards. Support and be the lead in Analytical and Chemical test method development and test method validations. Writing of SOPs, test methods, study protocols, reports and reviews. Training of lab analysts on analytical test method procedures and usage of equipment and documentation. | 10/20/2023 |
| 3865 | Physical Sciences Andover , MA Optical Engineer Bachelor’s degree in optical or mechanical engineering, physics or equivalent. Exp: 1+ years |
Physical Sciences Inc., a 100% Employee-Owned company located just north of Boston in Andover, seeks an Optical Engineer with professional experience to support development of emerging optical technologies. The candidate will support optical systems design, construction, and testing needs for illuminators, projectors, integrated spectrometers and/or metasurfaces. | 10/20/2023 |
| 3866 | Physical Sciences Andover , MA Experimental Physicist Bachelor or Masters degree in Physics, Applied Physics, Optics, or Related Discipline. Exp: entry level |
Physical Sciences Inc., located just north of Boston in Andover, MA, seeks an experimental physicist with experience in laser-based tools related to applications such as atom sensing, integrated photonics, or optical materials development. The candidate will join teams at PSI and contribute to invention, demonstration, and deployment of technology platforms targeting these application areas. The ideal candidate will have a bachelor’s or master’s degree in physics or related disciplines and should be interested in applied research and development with strong experimental, hardware, and leadership skills. | 10/20/2023 |
| 3867 | Physical Sciences Andover , MA Chemical Engineer Bachelor’s degree in chemical engineering or chemistry is required. Exp: 1+ years |
Physical Sciences Inc. is seeking a chemical engineer to join a multidisciplinary team of engineers and scientists driving innovation in the fields of energy, material science, and aerospace and defense. This individual will play a key role in growing a diverse portfolio of technologies funded by the DoD, DoE, and NASA. The applicant will assist with developing and scaling-up materials production from laboratory/batch processes to pilot-scale/continuous processes. Candidates should have a strong background in reaction kinetics, heat and mass transfer, separations, wet chemistry, and analytical instrumentation. | 10/20/2023 |
| 3868 | Physical Sciences Boston, MA Radio Frequency and Directed Energy Engineer Bachelor’s degree in Electrical Engineering, Physics, or a similar field required. Exp: Recent Graduates |
PSI currently seeks an individual with strong educational and profession experience in RF system engineering, manufacturing, and testing. A solid understanding of theoretical concepts and first principals is a must, as well as the ability to work independently. The ideal candidate will be multi-disciplinary, with strong abilities in systems engineering. This individual will be expected to interact across all engineering disciplines (RF, electrical, mechanical, manufacturing etc.) and develop technology at all stages of development (early stage research TRL 5-10 late stage development). | 10/20/2023 |
| 3869 | Physical Sciences Boston, MA Mechanical Engineer/R&D Entry level candidate with B.S. (or greater) in Mechanical Engineering. Exp: Entry Level |
Physical Sciences Inc., located just north of Boston in Andover, seeks an entry-level to mid-level engineer (B.S. in Mechanical Engineering or similar) to support R&D projects for advanced laser-based sensor systems. This Engineer will be a part of a multi-disciplinary team focused largely on the development and transition-to-production of optical sensing technologies used in environmental and industrial applications (e.g. greenhouse gas emissions reduction, process fluids sensors, standoff or airborne sensors). Recently, sensors developed and deployed include laser-based systems for the detection and quantification of ambient trace gases, or characterization of fuel streams, for the energy industry. | 10/20/2023 |
| 3870 | The Ritedose Corporation Columbia, SC Chemist I BS degree in Chemistry or related field. Exp: 1+ years |
The Chemist I is responsible for performing all the analytical testing related to raw materials, compounding activities, and final product testing including HPLC analysis in the Chemistry laboratory. Other responsibilities include sampling, testing, and releasing of utilities. - Tier 1 Products - Wet Chemistry - HPLC Beginner - GC Beginner | 10/20/2023 |
| 3871 | The Ritedose Corporation Columbia, SC Microbiologist I BS degree or 2 year technical degree in Microbiology or related field. Exp: 0 - 6 months |
The Microbiologist I is responsible for all duties related to performing environmental monitoring, personnel monitoring, microbial enumeration, microbial identification, and sampling of utilities. The Microbiologist I is also responsible for performing all the microbiological testing related to raw materials, utilities, and in-process product testing. Other responsibilities include data entry, data review, ensuring calibration of equipment, maintaining inventory of laboratory supplies, and maintaining the Microbiology laboratory by ensuring its cleanliness and order. Level 1 - Less than 6 months experience or no experience - Environmental Monitoring Completion - Utilities completion - Microbial Identification (subculture, Gram-stain, ID entry, VITEK MS assist) - Raw Material Testing including APIs | 10/20/2023 |
| 3872 | Surmodics Eden Prarie, MN Associate Quality Scientist B.S. or B.A. degree in chemistry, biology or appropriate discipline. Exp: 1 year |
The Associate QC Scientist is responsible for testing of raw materials, intermediates, and final products. Testing may be conducted for product release, stability testing, validation, and other purposes. This includes sample preparation, testing and data analysis according to established procedures. The Associate QC Scientist may also perform routine instrument repair and calibration. | 10/20/2023 |
| 3873 | uniQure Lexington, MA QA Specialist I Bachelor’s degree in Life Sciences or Engineering. Exp: 1-3 years |
The Quality Assurance Specialist I, supports the day-to-day quality operations via Manufacturing Clean Room presence, Material/Inventory QA Release, oversight of all elements of the Quality Management System (QMS), including but not limited to deviations, Corrective and Preventive Actions (CAPAs), investigations, change control, batch review, data integrity, and training in support of biologics manufacturing production. | 10/20/2023 |
| 3874 | uniQure Lexington, MA QC Sample Management Analyst Bachelor’s degree in Life Sciences or Engineering. Exp: 0-1 years |
The Quality Control (QC) Sample Management Analyst supports the day-to-day quality operations within the cGMP QC laboratories via oversight of all elements of sample management including but not limited to receiving, processing, storing, and retrieving all samples appropriately and promptly. This position supports the second shift at uniQure’s state of the art facility in Lexington, MA. | 10/20/2023 |
| 3875 | Acceleron Pharma Rahway, NJ Associate Scientist B.S. or M.S. degree in Chemical Engineering, Biomedical Engineering, Pharmaceutical Sciences or related discipline (expected no later than August 2024 Exp: 1+ years |
The successful candidate will be a passionate Scientist with strong academic fundamentals and a drive to develop new medicines to improve human health. In this role, the individual will be responsible for supporting the formulation development of new chemical entities as part of a matrix team from initial first in human formulations (suspensions, solutions, capsules, tablets) through final market formulation definition and manufacturing process robustness assessment. | 10/20/2023 |
| 3876 | Acceleron Pharma Rahway & Kenilworth, NJ Associate Scientist, Biologics Process Research & Development BS (or expected completion by May 2024) in Chemical/Biochemical/Biomedical Engineering, Biotechnology, Biochemistry, Microbiology, Structural biology, Exp: 1+ years |
As an Associate Scientist in BPR&D you will work with a highly collaborative team of scientists and engineers to design, develop and execute robust processes in support of early- to late-stage biological products. You will apply rigorous scientific principles to solve challenging problems focused on developing the best processes to deliver life-changing medicines to patients worldwide. You will also have an opportunity to contribute to additional areas of interest such as biophysical, process, economic and/or multivariate modeling as we are committed to leveraging digital ways of working to enhance our ability to design robust processes. | 10/20/2023 |
| 3877 | Acceleron Pharma West Point, PA Associate Scientist, Upstream Vaccine Process Development Must hold (or plan to complete by December 2023) a BS in Relevant Fields: Chemical Engineering, Biomedical Engineering, Biological Engineering, Bioeng Exp: 1+ years |
Applications are sought for a scientific opportunity in our Company's Vaccines Process Research and Development division. Under the direction of the group leader, this position will be responsible for the upstream process development of vaccine candidates. The successful candidate will perform lab-scale process development/scale-up studies, and develop robust, efficient, scalable cell culture processes for vaccine production. Duties may include: lab-scale fermentation or cell culture, in-process assay support, process scale-up and engineering, maintaining/coordinating raw material and equipment inventories to support development experiments, technology transfer to later stage development groups, and functioning as a key member of an early stage process development team. The incumbent is expected to function in a multi-disciplinary environment and to contribute subject matter expertise to various functional teams engaged in the development of the vaccine candidate. The successful candidate will be expected to demonstrate the ability to convey the results of their work in both verbal and written formats. In addition to the core duties outlined above, the candidate will be expected to keep careful notes, comply with all required training, and maintain focused attention on laboratory safety for themselves and their team. Position requires the employee to be willing to work with infectious agents and/or pathogens. Travel may be needed to support technology transfer. This position will require occasional off-hour and weekend work. | 10/20/2023 |
| 3878 | Santa Cruz Biotechnology Paso Robles, CA Research Assistant Bachelor of Science in Biology, Microbiology, Cellular Biology, Biochemistry, or similar field of study. Exp: entry level |
Santa Cruz Biotechnology has an immediate opening for an entry level Research Assistant at our Paso Robles, CA campus. This is a full time position with career advancement opportunities within the company. | 10/9/2023 |
| 3879 | Santa Cruz Biotechnology Santa Cruz, CA Research Assistant Bachelor of Science degree in Biology, Microbiology, Cellular Biology, Biochemistry, or similar field of study. Exp: entry level |
Santa Cruz Biotechnology has an immediate opening for an entry level Research Assistant at our Santa Cruz, CA campus. This is a full time position with career advancement opportunities within the company. | 10/9/2023 |
| 3880 | Santa Cruz Biotechnology Ketchum, ID Research Assistant Bachelor of Science degree in Biology, Microbiology, Cellular Biology, Biochemistry, or similar field of study. Exp: entry level |
Santa Cruz Biotechnology has an immediate opening for an entry level Research Assistant at our Ketchum, ID campus. This is a full time position with career advancement opportunities within the company. | 10/9/2023 |
| 3881 | ScienCell Research Laboratories Carlsbad, CA Associate Molecular Biologist Bachelor’s or Master’s degree in life science. Exp: one-year |
We are searching for an energetic and self-motivated candidate with a positive attitude and strong work ethic to fill our associate molecular biologist position in our R&D department. Responsibilities include, but are not limited to, working on cell-derived DNA, RNA, and proteins purification, gene expression analysis, performing PCR/RT-PCT/qPCR, SDS PAGE and UV spectrum for quantitation. Candidates should be familiar with electrophoresis, spectrophotometer, centrifugation and other basic laboratory techniques. General lab logistical skills such as record keeping, ordering supplies and ensuring general laboratory safety and cleanliness are also required. | 10/9/2023 |
| 3882 | SeaGen Everett, WA Quality Control Analyst I - LaunchPad Bachelor's degree in a relevant field. Exp: 0-2 years |
This role performs lab support activities and participates in routine and non-routine testing of environmental samples in cleanroom areas. Completes laboratory work for the support and release of Seagen’s products in a GMP testing environment. Must be able to work weekends, off-shifts, and overtime as required. Applicant must be willing and able to work reliably on a flexible schedule to meet the demands of the project. This position will transition to a shift schedule once qualification activities are complete. | 10/10/2023 |
| 3883 | Sestina Bio Burlingame, CA Research Associate II/III, HTS BS/MS in Biology, Chemistry, Biochemistry or Chemical Engineering Exp: 1-2 years |
We are seeking a Research Associate II/III in our Burlingame location. The candidate will be a part of the high-throughput screening group, with primary responsibility for running screening operations for high-value products made by engineered strains of E. coli, S. cerevisiae, and other microbes. In addition, the candidate will contribute to the development and optimization of new high throughput and microfermentation assays, including automated sample preparation. They will work collaboratively with the rest of the team to optimize strain performance using our GenoScalerTM technology platform in rapid phenotyping of microorganisms. This hands-on position requires a desire and ability to work as a part of a multidisciplinary team, the ability to follow SOPs and run consistent operations, and an interest in continuously developing and improving our ability to characterize production strain through high throughput screening. | 10/10/2023 |
| 3884 | Smithers Wareham, MA Associate Chemist I - Environmental Fate and Metabolism B.S. degree in chemistry or related field. Exp: 6 months |
Position is expected to perform a variety of routine tasks and often complex and difficult procedures independently and under supervision, in support of the conduct of normal laboratory operations. Individual is expected to detect and report problems in standardized procedures due to instrumental, sample, or test system failures. Performs a variety of routine, laboratory-based procedures. Responsible for understanding and routinely performing applicable Standard Operating Procedures, study specific protocol procedures and other laboratory assignments. This often includes recording instrument and apparatus readings on standard forms, preparation of test systems and recording and compiling laboratory data in real time in a complete and thorough manner for individual assignments. Responsible for maintaining cleanliness of the labs, storage and chamber areas as well as executing regular maintenance/calibration of equipment used on a regular basis. Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations as well as company policies. Duties are performed with minimal supervision. | 10/10/2023 |
| 3885 | Smithers Wareham, MA Assistant Biologist - Ecotoxicology - Smithers Wareham, MA Bachelors or better in Biology or related field. Exp: 1+ years |
Smithers Environmental Risk Sciences division is seeking an Assistant Biologist in the Ecotoxicology Department at our Wareham, MA location. Often, duties include recording instrument and apparatus readings, making observations of various biological effects in exposures and compiling study data books. Incumbent will be introduced to mathematical and statistical procedures used to reduce and analyze study data. Responsible for maintaining cleanliness of the labs, storage and culture areas including maintenance and calibration of equipment used in any of these settings. May require routine involvement in seawater and/or sediment collection. Assignments are completed with minimal supervision. Assists with organization, direction and training of technicians. Assists in coordinating internal requirements for testing (i.e. chemistry support, Quality Assurance, reporting). Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations and company policies.Smithers Environmental Risk Sciences division is seeking an Assistant Biologist in the Ecotoxicology Department at our Wareham, MA location. Often, duties include recording instrument and apparatus readings, making observations of various biological effects in exposures and compiling study data books. Incumbent will be introduced to mathematical and statistical procedures used to reduce and analyze study data. Responsible for maintaining cleanliness of the labs, storage and culture areas including maintenance and calibration of equipment used in any of these settings. May require routine involvement in seawater and/or sediment collection. Assignments are completed with minimal supervision. Assists with organization, direction and training of technicians. Assists in coordinating internal requirements for testing (i.e. chemistry support, Quality Assurance, reporting). Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations and company policies. | 10/10/2023 |
| 3886 | Smithers Wareham, MA Associate Chemist I - Environmental Fate and Metabolism B.S. degree in chemistry or related field. Exp: 6 months |
Description Job Summary Position is expected to perform a variety of routine tasks and often complex and difficult procedures independently and under supervision, in support of the conduct of normal laboratory operations. Individual is expected to detect and report problems in standardized procedures due to instrumental, sample, or test system failures. Performs a variety of routine, laboratory-based procedures. Responsible for understanding and routinely performing applicable Standard Operating Procedures, study specific protocol procedures and other laboratory assignments. This often includes recording instrument and apparatus readings on standard forms, preparation of test systems and recording and compiling laboratory data in real time in a complete and thorough manner for individual assignments. Responsible for maintaining cleanliness of the labs, storage and chamber areas as well as executing regular maintenance/calibration of equipment used on a regular basis. Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations as well as company policies. Duties are performed with minimal supervision. Description Job Summary Position is expected to perform a variety of routine tasks and often complex and difficult procedures independently and under supervision, in support of the conduct of normal laboratory operations. Individual is expected to detect and report problems in standardized procedures due to instrumental, sample, or test system failures. Performs a variety of routine, laboratory-based procedures. Responsible for understanding and routinely performing applicable Standard Operating Procedures, study specific protocol procedures and other laboratory assignments. This often includes recording instrument and apparatus readings on standard forms, preparation of test systems and recording and compiling laboratory data in real time in a complete and thorough manner for individual assignments. Responsible for maintaining cleanliness of the labs, storage and chamber areas as well as executing regular maintenance/calibration of equipment used on a regular basis. Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations as well as company policies. Duties are performed with minimal supervision. | 10/10/2023 |
| 3887 | Smithers West Trenton, NJ Scientist (PCR and Molecular Biology) MS in relevant field Exp: 1-2 years |
Description Smithers PDS LLC (Pharmaceutical Development Services) assists in the development of new medicines by providing bioanalytical services for all phases of drug development from discovery through approval and post market surveillance. PDS works with customers to develop new methods, validate existing methods, and perform the assays necessary to analyze samples from patients on more than 100 clinical trials. PDS is seeking a Scientist with experience in Molecular Biology to join our team. The successful candidate is able to apply prior experience and knowledge to successfully perform in a laboratory environment under regulated conditions. | 10/10/2023 |
| 3888 | Smithers Columbus, OH Associate Chemist I Bachelors or better in Chemistry. Exp: 1+ years |
Essential Functions: Cannabis sample processing of flower, concentrates, extracts, and infused products. Cannabis sample extraction & dilutions. Routine maintenance of laboratory equipment and instrument calibration. Wash glassware used by the laboratory. Accurate entry of sample data into LIMS. Production of laboratory reagents and stocks. Additional duties as assigned. | 10/10/2023 |
| 3889 | Smith & Nephew Columbia, MD Manufacturing Tech I Manufacturing Tech I Manufacturing Tech I Bachelor’s degree in a life science. Exp: 0+ years |
Responsible for hands-on execution of all activities in the manufacturing area including the processing and packaging of human tissue products for transplantation. All duties are performed in compliance with FDA cGMP/cGTP requirements, American Association of Tissue Banks (AATB) standards, and Osiris Therapeutics Inc. standard operating procedures (SOPs). The candidate should have a dedication to high standards of quality. | 10/10/2023 |
| 3890 | Spherotech Lake Forest, IL Manufacturing Associate Bachelor's degree in Chemistry or related field. Exp: 0+ years |
Spherotech, Inc. seeks a college graduate for a Technical Customer Support Representative opening. Duties include, but are not limited to providing customer/technical assistance and Microparticle application support. Responsibilities also include representing the company through trade shows, technical publications, and presentations. Required laboratory skills include: Analysis of Microparticles using particle sizers, flow cytometry, fluorescence spectrophotometry, and microscopy. | 10/10/2023 |
| 3891 | Spherotech Lake Forest, IL Quality Control Associate Bachelor's degree in Chemistry or related field. Exp: 1 year |
Spherotech, Inc. seeks a college graduate for a Quality Control Associate opening. Duties include final product inspection, documentation, Quality Control testing etc. This position requires a Bachelor's degree in Chemistry or related field and a minimum of 1 year of experience. We offer excellent benefits including paid vacation, health insurance, dental insurance, etc. Compensation commensurate with experience. | 10/10/2023 |
| 3892 | StageBio Frederick, MD Laboratory Technician I/II/III College degree preferred. Exp: 0+ years |
StageBio is seeking a full-time Laboratory Technician II to join our Frederick, Maryland facility. | 10/11/2023 |
| 3893 | StageBio Mount Jackson, VA Laboratory Technician I College degree preferred. Exp: 0+ years |
StageBio is seeking a full-time Laboratory Technician I to join our Mount Jackson, Virginia facility. | 10/11/2023 |
| 3894 | Sutro Biopharma South San Francisco, CA Research Associate, Analytical Development BS in analytical chemistry, biochemistry, molecular biology, chemistry, or related scientific field. Exp: 1+ years |
Sutro Biopharma, Inc. is looking for a Research Associate to join our Analytical Development group to support chromatography and mass spectrometry analyses for antibodies (mAb), bispecific antibodies (bsAb), antibody-drug conjugates (ADCs), immunostimulatory antibody-drug conjugate (iADCs) and cytokine derivatives. | 10/12/2023 |
| 3895 | Synlogic Cambridge, MA Quality Control Technician / Senior Quality Control Technician Bachelor’s degree. Exp: 0-2 years |
This is a lab-based role – based in Cambridge MA. Position reports to the Sr. Manger of Quality Control, and will be trained. | 10/12/2023 |
| 3896 | Takeda Boston, MA Research Associate II MS in Molecular Biology, Biochemistry, or Immunology (or equivalent). Exp: 0+ years |
Join Takeda as a Research Associate II where you will produce therapeutics in the areas of oncology, neuroscience and gastro intestinal diseases. You will also implement innovative ideas for cloning bi/multi-specific biologics designs to drive selection of leads and assist the group in implementing new automation technologies. As part of the Global Biologics Research, you will report to High Throughput Protein Production Research Scientist II, Global Biologics. | 10/12/2023 |
| 3897 | Takeda San Diego, CA Research Associate I, GI DDU BS degree in a scientific discipline, or equivalent. Exp: 0+ years |
Join Takeda as a Research Associate I where you will perform Molecular Biology techniques like RNA isolation and qRTPCR as well as in vitro assays (Luminescence-based and Meso scale ELISA). You will also support ongoing and future cell culture experiments to support drug discovery projects for liver disease and will work in an animal related research environment, record keeping of data, and inventory of sample and cell banks. As part of the, Liver Research team you will report to the Scientist II and work with Gastroenterology Drug Discover Unit (GI DDU). | 10/12/2023 |
| 3898 | Takeda Boston, MA Senior Research Associate I, Global Biologics MS in Biochemistry, Biology or a related field (or equivalent). Exp: 1+ years |
Join Takeda as a Senior Research Associate I where you will support the Therapeutic Generation and Screening (TGS) team of Takeda’s Global Biologics Department with demonstrated skills in molecular biology and automation. You will also work independently to generate DNA constructs to be used for expression/ purification of antibodies/ proteins, cell line generation and chimeric antigen receptors. This position will involve extensive use of automation for molecular cloning and plasmid DNA preparation. As part of the TGS team, you will report to the Principal Scientist and work with the Global Biologics organization. | 10/12/2023 |
| 3899 | Takeda Boston, MA Senior Research Associate, CMC Analytical Master’s degree in chemistry, biology, pharmacy, engineering or related pharmaceutical science. Exp: 0+ years |
Join Takeda as a Senior Research Associate, CMC Analytical where you will you will be empowered to develop, validate and transfer analytical methods to advance Takeda`s portfolio. You will also execute basic/routine experiments under limited supervision, plan basic experiments, and perform specialized/complex experiments with assistance from supervisor as appropriate. As part of the Analytical Development team, you will report to Sr Scientist, CMC. | 10/12/2023 |
| 3900 | Takeda Cambridge, MA Senior Research Associate/Engineer III Master degree in chemistry, biology, pharmacy, engineering or related pharmaceutical science. Exp: 0+ years |
You will be a part of the Synthetic Molecule Process Development team. SMPD is responsible for the development of robust, sustainable, and cost-effective processes for the manufacture of new synthetic molecule pharmaceuticals, along with methods for achieving and controlling high standards of purity and quality. As part of the team, you will seek to discover innovative solutions to manufacturing challenges. | 10/12/2023 |
| 3901 | Takeda Boston, MA Senior Research Associate I, In vitro Antibody Discovery MS in scientific discipline. Exp: 1+ years |
Join Takeda as a Senior Research Associate I where you will contribute to discovery of biologics using in vitro (phage) display approaches within the biotherapeutic generation and engineering group, using state-of-the-art discovery technology and creating novel treatments to positively impact patients’ lives in the fields of Oncology, Gastroenterology and Neuroscience. You will also contribute to discovery and engineering of therapeutic biologics including antibodies, sdAb and alternative formats through end-to-end process management, from vector design and library construction, to selection campaigns and screening. As part of the ,Biotherapeutic Engineering team you will report to the Senior Scientist and work with the Global Biologics organization. | 10/12/2023 |
| 3902 | Takeda Boston, MA Cell Therapy Processing Specialist/Senior Specialist Senior Cell Therapy Processing Specialist: Masters degree in chemistry, biotechnology, biology, engineering or related pharmaceutical science. Cell Th Exp: Senior Cell Therapy Processing Specialist: 1+ years; Cell Therapy Processing Specialist: BS: 1+ years; MS: 0+ years. |
The primary focus of the Cell Processing Specialist role will be cGMP cell therapy manufacturing at Takeda’s new cell processing facility in Cambridge, Massachusetts. This position will directly contribute to the successful delivery of novel cell products in support of human clinical trials. | 10/12/2023 |
| 3903 | Tapemark West Caldwell , NJ Equipment Reliability & Process Engineer (1st Shift) Bachelor’s degree in Engineering, Mechanical or Industrial Engineering Exp: 1 year |
Basic Office Setting – Exposure to Computer Monitor Ability to lift or move 25-49 pounds Occasional Travel Ability to Gown for Manufacturing I will abide by all cGMP, FDA and DEA regulatory standards Embrace safety as a value taking responsibility for the safety of themselves and their co-workers Work collaboratively with Production Manager and Director of Production to implement and sustain TPM system practices and culture Create training material and train operators and fabrication leadership on TPM systems and practices. Collaborate with production managers, engineering, and machine operators in the creation of troubleshooting guides, corrective maintenance guides and preventive maintenance procedures. Participate in daily management meetings to report and track equipment reliability metrics like OEE, MTTF & MTBF. | 10/12/2023 |
| 3904 | Tapemark West Caldwell , NJ Process Development Engineer (1st Shift) BS degree chemical or mechanical engineering or related field. Exp: 0-3 years |
Basic Office Setting – Exposure to Computer Monitor Physical Requirements – Not Applicable Occasional Travel Business Dress plus ability to Gown for Manufacturing I will abide by all cGMP, FDA and DEA regulatory standards Under supervision of senior associate, plan and execute process studies for feasibility, development/characterization (Design Of Experiments), and qualification of new products. Recommend changes to process conditions for product quality, throughput, and yield. Write master batch records, protocols, Standard Operating Procedures, process development reports, etc. Analyze data and assist in solving technical problems. Support Validation group with Failure Mode and Effects Analysis (FMEA) and Risk Assessments as needed. Maintain accurate and complete records of development activities in accordance with cGMP guidelines. | 10/12/2023 |
| 3905 | Terumo Cardiovascular Systems Elkton, MD Engineer I, Engineering Rotational Program Bachelor level or higher degree in an engineering discipline from an accredited university or college. Exp: Entry level |
The Rotational Engineer I – Engineering position is an entry level developmental engineering position for establishing a career progression in process, automation/machine and manufacturing engineering through the completion of a 3-year guided program consisting of sequential 1-year assignments in Process Engineering, Automation & Equipment Engineering, and Manufacturing Engineering under the mentorship of senior engineering leaders in each function. Within each assignment, the Rotational Engineer I – Engineering position will support on-going engineering activities by acquiring foundational engineering development skills necessary for the introduction and operation of new processes and equipment for the manufacture of cardiovascular interventional systems products. Key activities may include process design, specification and fabrication of equipment, process validation, process transfer into manufacturing, and continuous improvement and support of full scale production lines. At the successful completion of the 3-year rotational assignment, eligibility for promotion to the Engineer II will be attained. | 10/12/2023 |
| 3906 | Tessera Therapeutics Somerville, MA Research Associate II/Senior Research Associate, LNP Formulation MS in Chemistry, Chemical Engineering, Bioengineering, Pharmaceutical Sciences or related discipline. Exp: 0-3+ years |
Tessera Therapeutics is seeking a Research Associate II/Senior Research Associate, LNP Formulation to develop novel formulation processes to produce lipid nanoparticle (LNP) to support company’s in vitro and in vivo pre-clinical studies. In addition, the successful candidate will develop new techniques to characterize LNP batches. The ideal candidate will be proactive, enthusiastic, and show a passion for process development and formulation. The applicant should have strong communication and collaboration skills, along with a strong background in formulation process development and in LNP characterization. | 10/12/2023 |
| 3907 | Tris Pharma Monmouth Junction, NJ QC Analytical Chemist I Chemist I - Bachelors degree in Chemistry or related science field. Exp: 1-5 years |
The Quality Control (QC) Analytical Chemist I perform analytical testing of raw materials, packaging components, in-process (IP), finished product (FP), stability samples (ST), analytical method transfers and method verifications following analytical methods, United States Pharmacopeia (USP)/National Formulary Chapters, protocols, Standard Operating Procedures (SOPs) under current Good Manufacturing Practices (cGMPs) and company policies. Collaborating closely with, and under the direct supervision of Senior QC Analytical Chemists, Team Leads and QC Managers, the incumbent develops advanced analytical knowledge and expertise while carrying out laboratory work to support QC activities and performs special projects, as assigned | 10/13/2023 |
| 3908 | Tris Pharma Monmouth Junction, NJ Associate QC Analytical Chemist Bachelors in Chemistry or related scientific field. Exp: 0-3 years |
We have an immediate opening in our Monmouth Junction, NJ QC Lab for an (Associate) QC Analytical Chemist. This is an entry level scientific position and we will train qualified candidates who meet listed requirements. Recent college graduates are welcome to apply. The (Associate) Quality Control (QC) Analytical Chemist performs analytical testing of raw materials, packaging components, in-process (IP), finished product (FP), and/or stability samples (ST). She/he is also responsible for following Analytical Methods, current Good Manufacturing Practices (cGMPs), Protocols, Standard Operating Procedures (SOPs) and company policies. | 10/13/2023 |
| 3909 | Turn Biotechnologies Mountain View, CA Research Associate / Sr. Research Associate - Biology BS/MS in biology, biochemistry, molecular biology, or related discipline. Exp: one year |
Turn Biotechnologies is currently seeking a qualified, highly motivated individual for the position of Sr. Research Associate - Biology. This person will be a highly motivated and responsible individual whose primary purpose is to perform and assist with experiments, analyze data, maintain records, manage projects, maintain lab operations, and other duties as required to meet company goals. | 10/13/2023 |
| 3910 | United Therapeutics Manchester, NH Research Associate I/II - Tissue Systems Master’s Degree in cell biology, biomedical engineering or related field. Exp: (RA2) MS: 0+ years |
The Organ Manufacturing group (OMG) at Lung Biotechnology focuses on identifying, scoping, and delivering projects in support of our mission to build cutting edge technology for organ scaffold 3D bioprinting to address the unmet needs for transplantable organs. The Research Associate II-Tissue Systems will work with the direct supervisor to establish new experimental procedures and analytical metrics to characterize the biological outcomes of different lung cell types on 3D printed lung scaffolds. | 10/13/2023 |
| 3911 | United Therapeutics Manchester, NH Research Associate I/II- Tissue Systems Master’s Degree in cell biology, biomedical engineering or related field. Exp: (RA2) MS: 0+ years |
The Organ Manufacturing group (OMG) at Lung Biotechnology focuses on identifying, scoping, and delivering projects in support of our mission to build cutting edge technology for organ scaffold 3D bioprinting to address the unmet needs for transplantable organs. The Research Associate II-Tissue Systems will work with the direct supervisor to establish new experimental procedures and analytical metrics to characterize the biological outcomes of different lung cell types on 3D printed lung scaffolds. | 10/13/2023 |
| 3912 | United Therapeutics Silver Spring, MD Manufacturing Associate I - Fill Finish (1st Shift) Bachelor’s Degree in Arts/Sciences (BA/BS) in a scientific discipline or related field Exp: 1+ years |
The Manufacturing Associate I, Fill Finish provides process support for the production of drug products under strict adherence to cGMP, OSHA, and United Therapeutics policies and regulations in the Silver Spring, Maryland facility. | 10/13/2023 |
| 3913 | United Therapeutics Manchester, NH Research Associate I/II - Cell Production & Process Development Master’s Degree in cellular biology, developmental biology, biomedical engineering or related field. Exp: 0+ years |
The Research Associate II – Cell production and Process Development will perform and contribute to the design of cell studies as well as execute analytical methods to support the production and process development of iPS-derived cells and cellularized 3D scaffolds for the development of autologous 3D printed tissue engineered organs. | 10/13/2023 |
| 3914 | Verge Genomics South San Francisco, CA Research Associate - Neurodegenerative Disease Modeling MS preferably in neuroscience or cell-molecular biology, or a related scientific discipline. Exp: 0- 3 years |
The Target Validation and Exploratory Biology department is seeking a creative and driven research associate to develop state-of-the-art in vitro models representing neurodegenerative disorders using stem cell technology, organoids, 3D co-cultures and microfluidics. With your expertise in genome and stem cell engineering technologies, you will generate different brain cell-types and introduce disease mutations, pathway reporters, and drug target constructs. The candidate will profile quality, functionality and disease relevance of the in vitro brain models through imaging, single cell RNAseq, spatial transcriptomics, proteomics etc. You will benchmark the in vitro models by validating targets identified by Verge Genomics computational platform. This position plays a central role in the Verge Genomics pipeline, intersecting with target validation and drug discovery groups in advancing our pipeline of small molecules and biologics. | 10/13/2023 |
| 3915 | Vero Biotech Atlanta, GA Process Development Engineer Prefer master’s degree in Chemical Engineering. Exp: 1+ years’ |
The mission of this position is to extend the capacity of Vero technical operations group to achieve our strategic objectives, including timely product introductions and overall revenue targets. This role will need to effectively work with the VERO N2O4 Operations, Research & Development, Quality, Regulatory, and Supply Chain teams. Key Performance Indicators for this position include attainment of Throughput, Cost of Goods, Product Quality, Inventory targets, and On-time Delivery goals. | 10/13/2023 |
| 3916 | Vesigen Therapeutics Cambridge, MA Research Associate, Tissue Culture Core (Upstream PD) Bachelor’s or Associate’s degree in biology or related discipline. Exp: 1-3 years |
Vesigen is seeking a creative and highly motivated Research Associate to join our team and help advance the development of the company’s exciting ARMMs technology. The candidate will be an integral member of the R&D team, with opportunities to learn and contribute and develop numerous preclinical programs across several therapeutic areas. | 10/13/2023 |
| 3917 | BioPharmGuy Anywhere, US Contract Data Work some college Exp: 0 yrs |
We are looking for someone to help confirm mailing addresses in our directory. Mostly Googling. Can do work any time, any place. Must be able to accept payment via PayPal or Venmo. If interested, send a message through the contact form. Thanks! | 10/6/2023 |
| 3918 | Protomer Technologies Lebanon, IN Manufacturing Scientist - Lebanon API Manufacturing Master's Degree in STEM Discipline (Chemistry preferred). Exp: 1 year |
The Manufacturing Scientist is part of the TSMS (Technical Services/Manufacturing Science) team that provides the technical support required to achieve reliable and compliant manufacturing of API molecules. This role will be part of the Manufacturing Process Team for its respective area, providing daily oversight to ensure safe and reliable supply of medicines. The Manufacturing Scientist executes technical projects (experimental, modeling and/or production data analysis) to improve and optimize process control, yield, purity, and/or productivity. In addition, the manufacturing scientist should be capable and of setting up and executing a variety of experiments at laboratory scale and conducting research on manufactured product for process improvements and troubleshooting in the technical services and manufacturing sciences laboratory. | 10/5/2023 |
| 3919 | Protomer Technologies Indianapolis, IN Chemist- Nucleic Acid Synthesis Bachelor's and/or Master's degree Exp: 1+ years |
The Lilly Genetic Medicines Team is looking for collaborative creative and energetic problem solvers to join a multidisciplinary team at the front edge of innovation. You will join our fast-paced, interdisciplinary team as we utilize novel RNA/oligonucleotide based therapeutic modalities to enhance the Lilly portfolio. The successful applicant will utilize their knowledge and technical expertise to complement and enable core capabilities and help drive the revelation and development of RNA-based clinical candidates. Do you have an aptitude for innovative approaches and modalities in discovery and development focused on identifying impactful therapies for the patient? We want you on our team! | 10/5/2023 |
| 3920 | Protomer Technologies Boston, MA Plant Engineer Akouos Master's degree in Chemical, Mechanical, Electrical or industrial Engineering, or related field. Exp: 1 - 3+ years |
Join Akouos, a Lilly company, as a Plant Engineer III, The Plant Engineer III will serve as a Technical Lead for Capital projects, overseeing GMP manufacturing process equipment at the AKOUOS facility in Boston, MA. This individual will collaborate closely with Facilities and Engineering management, and equipment End Users to successfully drive projects to completion. The ideal applicant will thrive in a fast-paced, dynamic, and innovative environment, and will play a critical role in ensuring that projects are executed efficiently and effectively to meet objectives and timelines. Drive results by owning and completing medium to large scale projects with challenging timelines. Ensure appropriate root causes and corrective actions are identified through troubleshooting and investigation processes. | 10/5/2023 |
| 3921 | Protomer Technologies Boston, MA Associate Scientist, Early Preclinical Development Bachelor's Degree Exp: 0+ years |
The Early Preclinical Development (EPD) Team is seeking an Associate Scientist with experience in inner ear histology to support discovery and IND-enabling animal studies. The ideal candidate will have experience in histologic techniques specific to the inner ear, such as microdissection of the mouse and non-human primate (NHP) inner ear tissues into discrete anatomical regions, and further processing of these tissues using various histologic techniques, in addition to imaging, analysis, and preparation of data for presentation. Cross-functional work may be required to advance Company goals. The successful candidate will be self-motivated and creative, with a desire to succeed at the highest level in a highly collaborative and fast-paced environment. | 10/5/2023 |
| 3922 | Protomer Technologies Boston, MA Upstream Process Development Engineer Master's degree in Biochemistry, Chemical Engineering, Bioengineering or related discipline. Exp: 1-3+ years |
The Process Development group at Akouos is seeking an innovative Engineer to provide hands-on development support for the manufacturing of AAV-based gene therapy vectors. The ideal candidate for this position is an experienced Engineer with a strong background in AAV vector cell culture technologies and an excellent track record in gene therapy upstream process development. The successful candidate will actively participate in upstream process development, scale-up, process optimization, and process tech transfer for GMP manufacturing. The successful candidate will thrive in a collaborative, scientifically stimulating, and fast-pace work environment. | 10/5/2023 |
| 3923 | Protomer Technologies Indianapolis, IN Manufacturing Scientist – API Manufacturing Process Support Master's Degree in STEM Discipline (Chemistry focus preferred). Exp: 1 year |
The Manufacturing Scientist provides the technical support required to achieve the reliable and compliant manufacture of the Active Pharmaceutical Ingredient External Manufacturing (API EM) portfolio which includes raw materials, intermediates, enzymes and bulk drug substances. The API EM Manufacturing Scientist executes technical projects (experimental, modeling and/or production data analysis) to improve and optimize process control, yield, purity, and/or productivity. In addition, the manufacturing scientist should be capable and technically independent in setting up and executing a variety of experiments at the laboratory scale and conduct research on manufactured product for process improvements and troubleshooting in the technical services and manufacturing sciences laboratory. | 10/5/2023 |
| 3924 | Protomer Technologies Branchburg, NJ Research Associate-QC Biochemistry BS or MS in a related science such as a Biology or Biochemistry Exp: 0 - 5 years |
Conduct routine and non-routine analyses of in-process materials, raw materials, environmental/water samples, finished goods and stability samples by appropriate biochemical methods as assigned by supervisor. Perform routine QC responsibilities as needed. Apply acceptable cGMP practices during execution of all work tasks. Work independently with moderate supervisory guidance. | 10/5/2023 |
| 3925 | Pyxant Labs Salt Lake City, UT Analyst I Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1+ years |
Learns to analyze samples for various compounds and components in compliance with SOPs and regulatory agency guidelines. | 10/5/2023 |
| 3926 | Quanterix Billerica, MA Manufacturing Associate I BS in Chemistry, Biology or related Life Sciences Exp: 0+ years |
To continue our extraordinary growth, we are hiring a Manufacturing Associate I located in Billerica, MA. We are looking for an experienced and motivated candidate to join our Manufacturing team. This individual will work with a team of individuals to prepare solutions, conjugate beads, reconstitute antigens and perform filling activities to support a diverse assay menu. | 10/5/2023 |
| 3927 | Quanterix Billerica, MA Quality Control Analyst I Bachelor's Degree in Chemistry/Biochemistry/Biology or related field preferred Exp: 1+ years |
To continue our growth, we are hiring a Quality Control Analyst I located in Billerica, MA. This position will be part of our Quality Control team, responsible for a variety of activities including immunoassay testing on automated and semi-automated platforms, advanced data analysis, and prioritization and coordination and new product launch readiness in accordance with cGMP. | 10/5/2023 |
| 3928 | Quanterix Billerica, MA Manufacturing Associate I - 2nd Shift BS in Chemistry, Biology or related Life Sciences Exp: 1+ years |
To continue our extraordinary growth, we are hiring a Manufacturing Associate I located in Billerica, MA. We are looking for an experienced and motivated candidate to join our Manufacturing team. This individual will work with a team of individuals to prepare solutions, conjugate beads, reconstitute antigens and perform filling activities to support a diverse assay menu. | 10/5/2023 |
| 3929 | Quanterix Billerica, MA Downstream Manufacturing Associate I BS in Chemistry, Biology or related Life Sciences Exp: 0+ years |
To continue our extraordinary growth, we are hiring a Downstream Manufacturing Associate I located in Billerica, MA. We are looking for an experienced and motivated candidate to join our Manufacturing team. This individual will work with a team of individuals to prepare solutions, conjugate beads, reconstitute antigens and perform filling activities to support a diverse assay menu. | 10/5/2023 |
| 3930 | Quidel Athens, OH Protein Biochemist I Bachelor’s Degree in a biology, biochemistry, chemistry or other related science field. Exp: <1-year |
The Protein Biochemist I is responsible for the production of various proteins and their conjugation as well as antigen production and maintenance for downstream manufacturing, finished good catalog items, and custom orders in accordance with Quidel’s Quality System Regulations. This role is located in Athens, Ohio. | 10/5/2023 |
| 3931 | Quidel Carlsbad, CA Associate Process Group Chemist B.S./B.A. Life/Applied Sciences. Exp: 6 months |
As we continue to grow as QuidelOrtho, we are seeking an Associate Process Group Chemist, in accordance with forecasted requirements, participates in the manufacture of products within QSR and ISO regulations. This position reviews and reconciles documents and work orders, supports assigned projects with supervision, participates in product transfers, supports departmental troubleshooting and process improvement teams, and displays an improving working knowledge of business processes as they relate to manufacturing. This role is located in Carlsbad, CA onsite. | 10/5/2023 |
| 3932 | Quidel San Diego, CA Development Associate I BS/BA or equivalent in life sciences or chemistry. Exp: 1-3years |
As we continue to grow as QuidelOrtho, we are seeking a Development Associate I to join our research & new product development team. This person will participate in activities to support research and new product development. The position performs simple experiments as directed by Scientist or Manager. This position is onsite at our Summers Ridge office in San Diego, CA. | 10/5/2023 |
| 3933 | Quidel Athens, OH Associate Molecular Biochemist BA/BS in life sciences or MA/MS in related life sciences field. Exp: BS: 0-2 years; MS: 0 years |
As we continue to grow as QuidelOrtho, we are seeking an Associate Molecular Biochemist. Responsibilities include synthesis and analysis of small to mid-scale purified proteins and oligonucleotides and relevant in-process quality assessment activities, as well as supporting research and new product development utilizing these components (flex studies etc.). Responsibilities may include GMP protein/oligonucleotide analysis and providing support in addressing issues that may cause product supply interruptions. This role is also responsible for all in-process production activities for molecular assays. This position requires a high level of technical acumen, attention to detail and on the job training to become proficient across the multifaceted production spectrum required for advanced molecular production. This includes proficiency with autonomous production and ISO 13458/IVDR/510K quality requirements for over 500 molecular SKUs, specific handling of highly specialized equipment, proficiency in cGMP manufacturing techniques under Quidel’s Quality System. This position is located in Athens, Ohio | 10/5/2023 |
| 3934 | QuVA Pharma Bloomsbury, NJ Chemist 2nd Shift B.S. or M.S. degree in chemistry, biology or related field. Exp: 0- 2 years |
Responsibilities may include: Reads and understands SOPs and follow policy, procedure and applicable government regulations, such as current Good Manufacturing Practices (cGMP), DEA compliance, quality standards and safety requirements Provide analytical data in a timely manner. This includes understanding of Supervisor or Manager’s expectations Provide input to R&D SOPs to enhance the efficiency of the laboratory Keep accurate notebook records in accordance with SOPs, cGMP and current Good Documentation Practices (cGDP) requirements Communicate as needed any testing issues to either a Supervisor or Manager or to a cross-functional group such as Metrology | 10/5/2023 |
| 3935 | QuVA Pharma Bloomsbury, NJ Microbiologist 1st shift B.S. degree in related field (preferably Microbiology). Exp: 0-2 years |
Responsibilities may include: Compiles and interprets results of environmental monitoring tests and sterility results Conducts investigations of all non-conforming results Identifies environmental microbial isolates by classical techniques and automated identification methods to meet the requirements of the microbial environmental monitoring program Evaluates cleaning effectiveness on a routine basis to determine robustness of disinfection Develops and/or performs water sampling, including DI water, WFI and steam per the program (when needed) Performs and/or oversees surface and air sampling of the facility areas and equipment per the program Performs and/or oversees environmental monitoring of all facility areas in compliance with gowning requirements Validates methods and perform sterility (USP <71>), Scan RDI and endotoxin (USP <85>) testing for finished goods Performs growth promotion testing of media Prepares reports and communicate results for the environmental program per facility standards Trains and maintains current training status on required equipment and procedures Other duties as assigned | 10/5/2023 |
| 3936 | QuVA Pharma Bloomsbury, NJ Chemist 1st Shift B.S. or M.S. degree in chemistry, biology or related field. Exp: 0- 2 years |
Responsibilities may include: Reads and understands SOPs and follow policy, procedure and applicable government regulations, such as current Good Manufacturing Practices (cGMP), DEA compliance, quality standards and safety requirements Provide analytical data in a timely manner. This includes understanding of Supervisor or Manager’s expectations Provide input to R&D SOPs to enhance the efficiency of the laboratory Keep accurate notebook records in accordance with SOPs, cGMP and current Good Documentation Practices (cGDP) requirements Communicate as needed any testing issues to either a Supervisor or Manager or to a cross-functional group such as Metrology | 10/5/2023 |
| 3937 | Reata Pharmaceuticals Research Triangle Park, NC Manufacturing Associate (Recent Grad/Entry Level) – Upstream & Downstream Bachelor’s Degree (STEM preferred). Exp: Entry Level |
Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; with two main areas/disciplines – Upstream (Cell Culture) and Downstream (Purification). MAs perform these critical steps within Current Good Manufacturing Practice (cGMP) biosafety cabinets and cleanroom suites. | 10/5/2023 |
| 3938 | Minaris Regenerative Medicine Allendale, NJ QC Analytical Associate I BA/BS in a science or relevant field required. Exp: 1-2 years |
The Quality Control Analytical Associate serves as a support role to clinical and commercial production. The QC Analytical Associate will assist with process check point, stability, and release analytical testing to ensure that quality standards are upheld for all products produced at the facility. | 10/5/2023 |
| 3939 | Minaris Regenerative Medicine Allendale, NJ QC Analytical Associate I BA/BS in a science or relevant field required. Exp: 1-2 years |
The Quality Control Analytical Associate serves as a support role to clinical and commercial production. The QC Analytical Associate will assist with process check point, stability, and release analytical testing to ensure that quality standards are upheld for all products produced at the facility. | 10/5/2023 |
| 3940 | R & D Systems Minneapolis, MN Advanced Research Associate, Cell & Gene Therapy Master’s degree in a related field. Exp: up to 2 years |
This position will work within the Cell and Gene Therapy Applications group to provide scientific support of cell and gene therapy related Bio-Techne products. In this role, you would be responsible for assisting in lab maintenance, performing cell culture experiments, running molecular biology experiments, and writing standard operating procedures. This position is a fantastic opportunity for continuous learning and development in the rapidly evolving cell and gene therapy field. | 10/5/2023 |
| 3941 | R & D Systems Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
We are seeking an Advanced Research Associate for Bio-Techne’s Protein Purification department in Minneapolis. Our group supports 5000 different protein products used in academic research, pharmaceutical research, and all facets of biological science including: neurodegenerative diseases, stem cell research, glycobiology, developmental biology, etc. This individual will collaborate with many different departments to support the manufacturing processes of our products and contribute to the ongoing development of our growing and evolving portfolio. This position provides a potential for growth and career advancements within the company. This is a fantastic opportunity for an individual to gain problem solving and troubleshooting experience in a collaborative lab environment. This position also provides continuous learning and development, flexible working hours, and the ability to learn and apply a variety of lab techniques every day. | 10/5/2023 |
| 3942 | R & D Systems Minneapolis, MN Advanced Manufacturing Technician 4 year science degree. Exp: 1+ years |
The responsibilities of the Advanced Manufacturing Technician are to assist the laboratory staff with the process of building and manufacturing science products. This position will assist with a variety of tasks within a laboratory setting that may include filling containers with product, feeding a production machine, labeling product, recording data, operating equipment, formulation, and plate coating. This position offers 1st shift hours of 8:00am-4:30pmThe responsibilities of the Advanced Manufacturing Technician are to assist the laboratory staff with the process of building and manufacturing science products. This position will assist with a variety of tasks within a laboratory setting that may include filling containers with product, feeding a production machine, labeling product, recording data, operating equipment, formulation, and plate coating. This position offers 1st shift hours of 8:00am-4:30pm | 10/5/2023 |
| 3943 | R & D Systems Minneapolis, MN Advanced Manufacturing Technician Bachelor degree. Exp: 1-3 years |
The responsibilities of a Manufacturing Technician are to support the laboratory staff with the process of building and manufacturing science products. This position will perform a variety of tasks within a laboratory setting that may include labeling, recording data, operating equipment, formulation and plate coating. | 10/5/2023 |
| 3944 | R & D Systems Minneapolis, MN RA - Advanced Research Associate Master’s degree. Exp: minimal experience |
In this role, you would be responsible for the development and execution of QC test method validations for a variety of products, utilizing a wide variety of laboratory techniques. This position also assists in troubleshooting investigations and process improvement projects. As an Advanced Research Associate, you will also participate in cross-functional teams focused on new product introduction. | 10/5/2023 |
| 3945 | R & D Systems Minneapolis, MN Advanced Research Associate, Molecular Biology Master’s degree in Molecular Biology. Exp: 0-2 years |
The responsibilities of this position are to assist the protein product development team in the area of recombinant protein expression. This includes the preparation of eukaryotic expression vectors, cell culture, and screening procedures. The successful candidate will perform various techniques such as DNA preps, sub-cloning, mammalian and insect cell culture, transfections, Western blotting, ELISA, and flow cytometry. They will also prepare buffers and reagents, assist in cleaning and maintenance of the laboratory and equipment, and perform other general lab duties as assigned. | 10/5/2023 |
| 3946 | R & D Systems Minneapolis, MN Advanced Research Associate, Mammalian Cell Culture Bachelor’s degree in a biological science. Exp: 0 to 2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for recombinant protein production, media and supplement preparation, and additional duties as assigned. This position requires a Sunday through Thursday workweek. | 10/5/2023 |
| 3947 | Roche Seattle, WA Lab Assistant I Bachelor’s degree focused in Biology, Biotechnology, Biochemistry, Chemistry, Physics or Engineering field preferred. Exp: 1+ years |
Roche Diagnostics acquired Stratos Genomics (SBX Nanopore Sequencing) in 2020 for its novel Sequencing by eXpansion (SBX™) technology. SBX™ uses unique applications from chemistry, biochemistry, and protein engineering to sequence DNA by nanopore in rapid time with high accuracy and low cost. You will join the Central Service team and assist in the day-to-day operations of the company. The Central Service team plays an integral role within the company. Members are passionate and dedicated to our SBX™ technology and the impact high throughput, low-cost DNA sequencing will have on patient outcomes. We are looking for individuals who share this passion and are excited to join a dynamic team. Please include a cover letter outlining why you want to work with us, your specific interest in our technology, and how you would contribute. | 10/5/2023 |
| 3948 | SAMDI Tech Chicago, IL Research Assistant B.S. in biology, biochemistry, chemistry, or related field. Exp: 0-3 years |
The Research Assistant will be an active member of our dynamic Research Team. The Research Team leads target/enzyme-based projects for biotech and pharma clients to develop biochemical assays for high-throughput screening and characterization of drug candidates and reaction mechanisms. | 10/6/2023 |
| 3949 | Sangamo Therapeutics Richmond, CA Research Associate (CONTRACT) B.S. or higher in biology, virology, biochemistry, process engineering or related field. Exp: 1+ years |
Sangamo Therapeutics is seeking a talented temporary Research Associate to fill an open position in our Vector Core Production Group. Tasks would include viral vector production using mammalian tissue culture cells and vector purification by ultracentrifugation or column chromatography. Maintenance of our production and inventory database is also required. Analysis of the viral vectors by qPCR and gels may also be performed. The position requires adaptability, excellent planning and communication skills as well as the ability to work in a fast-paced, team-oriented, multidisciplinary environment. | 10/6/2023 |
| 3950 | Sangamo Therapeutics Brisbane, CA Research Associate – Bioassay Analytical Development (Contract) BS/MS in Biological Sciences such as Molecular Biology, Immunology, Virology, or related discipline. Exp: 1 year |
We are seeking a highly motivated Research Associate to support the development of our Adeno-associated virus (AAV) gene therapy products and gene-edited cellular therapies. In this role, the candidate will contribute to developing and qualifying a new cellular platform to enable a variety of Sangamo’s cell and gene therapy development programs. This is a laboratory-based position that requires creativity, organization, attention to detail, excellent communication and presentation skills, and a capacity for constant innovation in pursuit of company goals. The ideal candidate will be experienced in using mammalian cells to develop appropriate cell models to support cell-based assays along with a fundamental understanding of ICH guidelines for the method qualification. The environment is exciting, fast-paced and offers the opportunity to work at the cutting edge of cell and gene therapy. | 10/6/2023 |
| 3951 | Sanofi Genzyme Framingham, MA Research Associate, Genomic Medicine Bioanalytics BS in biological sciences or related field. Exp: 1 – 3 years |
The Research Associate is responsible for executing test methods under control of established procedures. Specifically, performing in-process and release testing of cellular therapies out of our 45 NYA manufacturing facility. Additional functions will include interpretation of data, preparation of test documentation, and management of analytical databases. We are looking for a candidate that is capable of learning quickly with the goal of executing analytical methods and managing assigned test schedules, with excellent communication skills. The position is located in Framingham, MA. | 10/6/2023 |
| 3952 | Sanofi Genzyme Framingham, MA Senior Research Associate - Biologics Drug Product Development Master’s degree in biochemistry, pharmaceutical science, chemical or protein engineering, or related field. Exp: 0+ years |
The senior research associate (SRA) will be part of Global Drug Product Development and Manufacturing, supporting biologic drug product formulation and process development. The SRA will play a critical role in supporting laboratory-based studies working on different facets of drug product formulation and process development, across multiple modalities including monoclonal antibodies (mAb), multi-specific antibodies, therapeutic enzymes, and fusion proteins. Formulation work would include both liquid and lyophilized formulation development, and process characterization from early phase 1 through phase 3 drug product development. | 10/6/2023 |
| 3953 | Sanofi Genzyme Waltham, MA Senior Research Associate, Genomic Medicine Unit - BioProcess Analytics Masters degree in biological sciences. Exp: 0+ years |
The BioProcess Analytics group located in Waltham, MA is seeking a highly motivated Senior Research Associate to join our team of talented individuals. The successful candidate must have a basic understanding of analytical method development and technologies, with scientific knowledge in cell and gene therapy analytics preferred. The candidate must be highly motivated, well organized, able to execute studies independently, collaborative, and able to communicate effectively with a cross-functional team. | 10/6/2023 |
| 3954 | Sanofi Genzyme Framingham, MA Senior Research Associate - Cell Line Development Master’s degree in Biology, Cell Biology, Biotechnology or related discipline. Exp: 0+ years |
We are seeking a highly motivated candidate to join a high-performing, collaborative group working on different aspects of CHO cell line development. Responsibilities will focus on generation and evaluation of cell lines producing recombinant biologics, including monoclonal antibodies and other protein formats, and performing experiments to help drive process improvements. Work will directly support development projects in Sanofi’s pipeline. | 10/6/2023 |
| 3955 | Sanofi Genzyme Waltham, MA Research Associate - Cell Culture Process Development - Genomic Medicine Unit Bachelor’s degree in biological science or engineering discipline. Exp: 1+ years |
The Genomic Medicine Unit (GMU) CMC group at Sanofi is dedicated to the establishment of best in class manufacturing platforms to support development of life-changing advanced cell and gene therapy products, including recombinant AAV vectors and cell therapy products. This organization encompasses vector and cell line engineering, upstream and downstream process development, analytics, and clinical manufacturing support. The cell culture process development group is responsible for viral vector production optimization and development of next generation production platforms to support high dose therapeutic products. The group is seeking a motivated Research Associate to join the team. | 10/6/2023 |
| 3956 | Sanofi Genzyme Framingham, MA Senior Research Associate - QC, Genomic Medicine Bioanalytics - CT Master’s degree in Biology/Biochemistry or related discipline. Exp: 0+ years |
This position resides within the Genomic Medicine Unit (GMU), a part of Sanofi’s CMC Development organization. The GMU Analytical Development group has the overall responsibility to establish phase appropriate control strategies and to develop, qualify, and validate robust analytical methods to support release and characterization testing of different cell therapy candidates. The group supports cGMP-compliant in-process Quality Control (QC) support of cGMP Manufacturing cutting edge methods such as flow cytometry. The selected candidate will execute rapid turnaround cGMP testing of in-process materials. In addition, contribute to method improvement, qualification, and drug product testing prior to going to clinical trials. The candidate will work with the team to facilitate these goals. This group will be in Framingham working onsite. This position will be a rotating morning shift (9am-7pm), 4 days per week, and will be required to work two weekends a month. | 10/6/2023 |
| 3957 | Sarepta Therapeutics Columbus, OH Research Associate I/II, Immunology B.A. or B.S. degree in Biological Sciences or related discipline. Exp: 1-3 years |
Sarepta Therapeutics is seeking a motivated Research Associate I/II (RA I/II) that will perform experiments under the direction of Immunology lab members, collecting and verifying research data as well as performing assays to support clinical and non-clinical trials. The RA I/II will help organize and prepare research materials as well as assist in maintaining equipment, documentation, and inventory. This is a lab-based position that contains occasional weekend and late evening work. | 10/6/2023 |
| 3958 | Omniome Menlo Park, CA Scientist, Research Associate (Molecular) Bachelor's degree in Molecular Biology, Biochemistry or related field. Exp: 1 year |
Pacific Biosciences is looking for a Scientist, Research Associate (Molecular) who will serve as part of the product development team, contributing to the development of Single Molecule Sequencing products for the company’s real-time sequencing platforms. | 9/26/2023 |
| 3959 | Omniome San Diego, CA Engineer II, Systems Integration Masters degree Exp: 1-3 years |
Pacific Biosciences seeks a talented, driven, and experienced system integration engineer to join the System Integration and Verification Team. The candidate will be responsible for integrating and testing all aspects of the system including hardware, software, and consumables. | 9/26/2023 |
| 3960 | OmniSeq Durham, NC Flow Cytometry Analyst Bachelors in Medical Technology or Bachelors in chemical, physical or biological science. Exp: BSMT: 0+ years; BS: 6 months |
$5,000 SIGN ON BONUS FOR EXTERNAL CANDIDATES. We are offering exciting opportunities to join our team as a Flow Cytometry Analyst - Technologist in Research Triangle Park at the Center for Molecular Biology and Pathology, Durham, NC. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". This Analyst will work alongside a highly trained staff with the latest technology. Our services are performed with the utmost care, expertise, integrity and respect for the patient. The work schedule for this position will be Wednesday-Saturday 10:00am-8:30pm, 1st shift. | 9/26/2023 |
| 3961 | OmniSeq Richmond, VA Technologist - Microbiology Associate degree in Medical Lab Science OR Bachelor degree in chemical, physical or biological science. Exp: 6 months |
Are you looking to embark on a new challenge in your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technician OR Technologist in Richmond, VA. In this position you will work in a Microbiology lab. The work schedule for this position will be: 2nd shift Monday-Friday 1pm-9:30pm | 9/26/2023 |
| 3962 | OmniSeq Research Triangle Park, NC ToxAssure Technologist - 1st Shift Bachelor's degree in Biology, Chemistry, Medical Technology or a related life science. Exp: 1 year |
Labcorp is seeking a ToxAssure Technologist or Technologist Trainee to join its team in Research Triangle Park, NC! This position will be working in the ToxAssure lab which performs urine medical drug monitoring testing. This is a great opportunity to join an innovative organization and receive targeted one-on-one training that will help the individual grow their career in the Toxicology Clinical Laboratory industry! The work schedule for this position will be 1st shift - Sunday-Thursday, 7:00 am – 3:30 pm | 9/26/2023 |
| 3963 | OmniSeq Burlington, NC Technologist for Chemistry Bachelor's degree Biology, Chemistry, Medical Technology or related. Exp: 1 year |
$2,500 Sign-On Bonus External Candidates Only! Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist for Chemistry department located in Burlington NC! In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". The schedule for this position will be: 1st shift, Saturday, Sunday, & Monday, 7:00am-7:30pm. | 9/26/2023 |
| 3964 | OmniSeq Greenfield, IN Research Assisatnt I - Cell Based and Immunology Team BS/BA degree in science or related field Exp: 0+ years |
Executes basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 9/27/2023 |
| 3965 | OmniSeq Greenfield, IN Research Assistant I BS/BA/BSc degree in science or related field Exp: 0+ years |
Executes basic Molecular BioA (Mol BioA) laboratory procedures under the oversight of experienced personnel. | 9/27/2023 |
| 3966 | OmniSeq Greenfield, IN Research Assistant I - Protein Chemistry BS/BA degree in science or related field Exp: 0+ years |
If you have a passion for science and working in a dynamic and fast paced lab with a cohesive team, the Research Assistant position will take you to the next level in your career. We have an excellent opportunity for someone to join our Protein Chemistry team in Greenfield, IN. In this role you will learn to execute basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 9/27/2023 |
| 3967 | Pacific Edge Hummelstown, PA Laboratory Technician Bachelor's degree in medical technology, chemical, physical, or biological sciences. Exp: 1 year |
Pacific Edge Diagnostics USA, an innovative cancer detection testing company is seeking a talented Clinical Laboratory Technician to join its team. The Clinical Laboratory Technician's primary responsibility will be to perform molecular clinical testing (from specimen receipt through reporting patient results), as well as general lab maintenance. | 9/28/2023 |
| 3968 | Pacira Biosciences San Diego, CA QA Associate 1 BS/BA degree in scientific discipline from an accredited college or university. Exp: 1 year |
This person is to assist and support the organization with GMP compliance, monitoring conformance to established quality assurance processes and GMP standards for manufacturing. | 9/28/2023 |
| 3969 | Pall New Port Richey, FL Manufacturing Engineer Bachelor of Science degree in Manufacturing, Mechanical, Industrial, and/or Aerospace Engineering or other related engineering field, required. Exp: 1+ years |
The Manufacturing Engineer is responsible for improvements within value streams of responsibility, in line with yearly targets in the areas of Safety, Internal and External Quality, On-Time Delivery / Lead Time reduction, and Productivity. This position is part of the Aerospace machine shop department and will be located onsite (full-time) in New Port Richey, FL. | 9/28/2023 |
| 3970 | Paradigm Diagnostics Marshfield, WI Clinical Laboratory Technician - Rare Disease Sequencing Laboratory Bachelor's degree in a chemical, physical, biological or clinical laboratory science or medical technology from an accredited institution. Exp: 0+ years |
The Clinical Laboratory Technician is responsible for performing standard laboratory procedures within the assigned department/laboratory. The Clinical Laboratory Technician will analyze data and may assist with research and development. This incumbent will be relied upon to follow laboratory protocols and maintain high quality levels. This role is located onsite in Marshfield, WI and works in our Sequencing Laboratory. The training for this role is 8 weeks Monday-Friday 8am-4:30pm. After training, the shift options are: Rotating 4-day/10-hour shift. Wednesday-Friday/Tuesday 7am-5:30pm with every 3rd weekend, 6:00am-4:30pm. 4-day/10-hour shift. Tuesday-Friday 12:00pm-10:30pm. | 9/28/2023 |
| 3971 | Par Pharmaceutical Horsham, PA Manufacturing Associate II, Downstream Processing BS degree Exp: 1+ years’ |
The Manufacturing Associate II, Downstream Processing works in a hands-on capacity in the cGMP purification and production support areas to manufacture collagenase clostridium histolyticum bulk drug substance (CCH BDS). This role authors and revises manufacturing & process documentation and is responsible for supporting necessary purification and production-related activities, including validation and development work as needed. | 9/28/2023 |
| 3972 | Par Pharmaceutical Horsham, PA Manufacturing Associate II, Upstream Processing BS degree Exp: 1+ years’ |
The Manufacturing Associate II, Upstream Processing works in a hands-on capacity in the cGMP fermentation and production support areas to manufacture collagenase clostridium histolyticum bulk drug substance (CCH BDS). This role authors and revises manufacturing and process equipment documentation and is responsible for supporting necessary fermentation and production activities, including validation and development work as needed. | 9/28/2023 |
| 3973 | Par Pharmaceutical Rochester, MI Chemist II (Weekend Shift) Master’s Degree in chemistry, chemical engineering or related field Exp: 1+ years’ |
The Chemist II, under general supervision, performs QC laboratory chemical analyses of raw materials, in-process materials, stability & finished products, and testing to support process validation. Detects, participates and reports on OOS/OOT/NOE and other investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. May train less senior staff. | 9/28/2023 |
| 3974 | Parse Biosciences Seattle, WA Research Associate I - Single Cell Genomics BA or BSc in molecular biology (or related field) Exp: one year |
As a Research Associate at Parse Biosciences, you will work at the cutting edge of molecular biology and genomics as part of a collaborative team. You will design and perform experiments to improve our existing single-cell RNA-sequencing kits as well as demonstrate new applications for our kits. You will also share responsibilities in organizing inventory, assembling kits, testing kits internally, reagent quality control, and maintaining the lab. | 9/28/2023 |
| 3975 | Pharmaron San Diego, CA In Vivo Research Associate I, PK BS Exp: 1-year |
Pharmaron (San Diego) is seeking to hire an outstanding candidate to join our PK department at the Research Associate I level. The Research Associate will play an important role by supporting in vivo pharmacokinetic studies. Primary responsibilities: This position requires a broad knowledge of anatomy, physiology, and biochemistry to help develop and support in vivo models to screen therapeutics and devices being developed for various disorders. Experience with surgical, dosing, and sampling techniques is required | 9/29/2023 |
| 3976 | Pharmaceutics International Hunt Valley, MD Aseptic Manufacturing Technician, Formulation Bachelor’s degree Exp: 1 year |
The Manufacturing Technician is responsible for the implementation of routine production and manufacturing procedures to support processes and ensure compliance with regulatory requirements. The Associate will work with the Drug Product team to ensure the successful completion of various cGMP activities. The Associate will partner in optimizing both technical aspects as well as quality systems which governs cGMP manufacturing. | 9/29/2023 |
| 3977 | Pharmaceutics International Hunt Valley, MD QC Microbiologist I- 2nd Shift B.S / M.S. in a life sciences discipline Exp: 0-2 years |
Executes the activities of QC Microbiology Laboratory by following approved microbiological and chemical test procedures and ensuring their delivery in an accurate and timely manner following proper safety precautions. | 9/29/2023 |
| 3978 | Pharmaceutics International Hunt Valley, MD Manufacturing Equipment Engineer Bachelor of Science in Engineering, mechanical engineering preferred Exp: 1 – 5 years |
The Manufacturing/Equipment Engineer is responsible for aspects of growing and improving the facility and equipment at our development and manufacturing sites. Most of the process will be liquid formulations manufactured under single-use production concept, in cleanroom environment. This role is involved in onboarding new process equipment, working closely on the ground with production and development personnel, organizing the production process equipment layout, and coordinating with other departments to ensure the validated status of process equipment. All work to be carried out in compliance with cGMP and company standard operating procedures and policies. | 9/29/2023 |
| 3979 | Pharmaceutics International Hunt Valley, MD QC Microbiologist I- 3rd Shift B.S / M.S. in a life sciences discipline Exp: 0-2 years |
Executes the activities of QC Microbiology Laboratory by following approved microbiological and chemical test procedures and ensuring their delivery in an accurate and timely manner following proper safety precautions. | 9/29/2023 |
| 3980 | Phitonex Middleton, WI Entry Level Scientist Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 9/29/2023 |
| 3981 | Phitonex Middleton, WI Entry Level Chemist Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 9/29/2023 |
| 3982 | Phitonex Middleton, WI Entry Level Biochemist Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 9/29/2023 |
| 3983 | Phitonex Rockville, MD Lab Technician I Prefers BS in a Biological Science. Exp: 1 yr |
This position is within the Fisher BioServices business unit of Thermo Fisher Scientific. The Laboratory Technician will assist in manual and automated laboratory processing of biological materials, including aliquoting and sample preparation. | 9/29/2023 |
| 3984 | Phitonex Plainville, MA Engineer I, Manufacturing Engineering B.S. degree in mechanical engineering, biochemical engineering, chemical engineering, electrical engineering or related engineering field preferred. Exp: Entry level to 2 years |
The Engineer I, Plant will be vital in supporting the groundbreaking VVS commercial facility in Plainville, MA. This position will play an important operations support role in the site Facilities and Engineering team where they will support manufacturing, laboratory and warehouse operations in Plainville, MA. | 9/29/2023 |
| 3985 | Phitonex Lexington, MA Plant Engineer I Engineering Degree (required) in relevant discipline is strongly preferred (Bachelor of Science degree in electrical, chemical, mechanical, or maritim Exp: 1 year |
Job Description At Viral Vector Services (VVS), a division of Thermo Fisher Scientific, we deliver from process development through commercial supply, we offer the expertise and resources vital to help clients deliver innovative gene therapies. Placed in the forefront of our leading and innovative Cell and Gene Therapy business enabling clients to cure genetic, rare, and otherwise untreatable diseases | 9/29/2023 |
| 3986 | Phitonex Cambridge, MA Process Engineer I, Manufacturing Technical Services - Upstream Bachelor’s degree (required) in biochemical or chemical engineering, pharmaceutical science or a related scientific discipline such as chemistry or bi Exp: 0-2 years |
US - Massachusetts - Cambridge Responsible for the support of clinical and commercial drug manufacturing at the viral vector manufacturing facility located in Cambridge, MA. Scope includes supporting the at-scale manufacture of late-stage and commercial gene therapy drugs from both a process and equipment standpoint with a focus on the upstream process and technology. Individual will join an experienced team of process engineers working closely with groups such as manufacturing, quality assurance, quality control, and validation. | 9/29/2023 |
| 3987 | Plex Pharma San Diego, CA Research Associate, Biology & Protein Chemistry BS or MS in molecular and biology, protein chemistry or related field. Exp: 1-3 years |
Plex Pharmaceuticals (www.plexpharma.com), a biotechnology company with a focus on developing novel drugs targeting misfolded and aggregated proteins, has an immediate opening for a Research Associate. The successful candidate will contribute to drug discovery efforts by performing cloning, expression and purification of protein drug targets, as well as assisting in assay development and characterization of compounds. | 9/29/2023 |
| 3988 | PPD Middleton, WI Associate Scientist - Microbiology - 2nd Shift Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1+ years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 9/29/2023 |
| 3989 | PPD Middleton, WI Assistant Scientist - Microbiology 2nd Shift Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 9/29/2023 |
| 3990 | PPD Devens, MA Associate Scientist - ELISA, HPLC Bachelor's degree in Biochemistry, Biotechnology, Analytical Chemistry, or equivalent and relevant formal academic / vocational qualification. Exp: 0-2+ years |
You will be responsible for supporting analytical activities within Biologics Process Development (PD). The role will involve supporting in-process analytical testing, delivering results within customer and project timelines, assay harmonization activities within the network groups, and evaluation of new analytical technologies. You will have excellent communication skills, is a team player, and have experience in Bioanalytical techniques as they apply to Biologics and related process impurities. Techniques of interest include Capillary Electrophoresis, Liquid Chromatography, and ELISAs. A reasonable appreciation of upstream and downstream process development activities is highly desirable. The role will provide Analytical support within PD. The candidate will work closely with PDA team members and Process Development to deliver quality analytical data in a timely manner. | 9/29/2023 |
| 3991 | PPD Providence, RI Associate Scientist - Mechanical Testing Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar. Exp: 0 to 1+ years’ |
Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. | 9/29/2023 |
| 3992 | Principia Biopharma Waltham, MA Research Associate, Purification Process Development Bachelor’s degree in biological science or engineering discipline. Exp: 1+ years |
The Genomic Medicine Unit (GMU) Chemistry, Manufacturing and Control (CMC) group at Sanofi is dedicated to the establishment of best-in-class manufacturing platforms to support development of life-changing advanced cell and gene therapy products, including recombinant AAV, non-viral vectors, and cell therapy products. The GMU purification process development group is responsible for the development of AAV processes and for supporting viral vector purification from next-generation production platforms to enable high-dose gene therapy programs. The Research Associate, Purification Process Development role requires leadership both inside and outside the laboratory and will rely on industry expertise and the exploration of novel technologies to build robust and efficient purification processes consistent with patient safety standards. We are looking for a motivated candidate with good communication skills and desire to learn advanced purification methods and contribute to organizational goals. | 9/29/2023 |
| 3993 | Principia Biopharma Framingham, MA Senior Research Associate - Biologics Drug Product Development Master’s degree in biochemistry, pharmaceutical science, chemical or protein engineering, or related field. Exp: 0+ years |
The senior research associate (SRA) will be part of Global Drug Product Development and Manufacturing, supporting biologic drug product formulation and process development. The SRA will play a critical role in supporting laboratory-based studies working on different facets of drug product formulation and process development, across multiple modalities including monoclonal antibodies (mAb), multi-specific antibodies, therapeutic enzymes, and fusion proteins. Formulation work would include both liquid and lyophilized formulation development, and process characterization from early phase 1 through phase 3 drug product development. | 9/29/2023 |
| 3994 | Principia Biopharma Framingham, MA Senior Research Associate - Cell Line Development Master’s degree in Biology, Cell Biology, Biotechnology or related discipline. Exp: 0+ years |
We are seeking a highly motivated candidate to join a high-performing, collaborative group working on different aspects of CHO cell line development. Responsibilities will focus on generation and evaluation of cell lines producing recombinant biologics, including monoclonal antibodies and other protein formats, and performing experiments to help drive process improvements. Work will directly support development projects in Sanofi’s pipeline. | 9/29/2023 |
| 3995 | Principia Biopharma Framingham, MA Senior Research Associate - QC, Genomic Medicine Bioanalytics - CT Master’s degree in Biology/Biochemistry or related discipline. Exp: 0+ years |
This position resides within the Genomic Medicine Unit (GMU), a part of Sanofi’s CMC Development organization. The GMU Analytical Development group has the overall responsibility to establish phase appropriate control strategies and to develop, qualify, and validate robust analytical methods to support release and characterization testing of different cell therapy candidates. The group supports cGMP-compliant in-process Quality Control (QC) support of cGMP Manufacturing cutting edge methods such as flow cytometry. The selected candidate will execute rapid turnaround cGMP testing of in-process materials. In addition, contribute to method improvement, qualification, and drug product testing prior to going to clinical trials. The candidate will work with the team to facilitate these goals. This group will be in Framingham working onsite. This position will be a rotating morning shift (9am-7pm), 4 days per week, and will be required to work two weekends a month. | 9/29/2023 |
| 3996 | ProteinSimple Minneapolis, MN Advanced Research Associate, Molecular Biology Master’s degree in Molecular Biology or equivalent. Exp: 0-2 years |
The responsibilities of this position are to assist the protein product development team in the area of recombinant protein expression. This includes the preparation of eukaryotic expression vectors, cell culture, and screening procedures. The successful candidate will perform various techniques such as DNA preps, sub-cloning, mammalian and insect cell culture, transfections, Western blotting, ELISA, and flow cytometry. They will also prepare buffers and reagents, assist in cleaning and maintenance of the laboratory and equipment, and perform other general lab duties as assigned. | 9/29/2023 |
| 3997 | ProteinSimple Minneapolis, MN Advanced Research Associate, Mammalian Cell Culture Bachelor’s degree in a biological science. Exp: 0 to 2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for recombinant protein production, media and supplement preparation, and additional duties as assigned. This position requires a Sunday through Thursday workweek. | 9/29/2023 |
| 3998 | NorthEast BioLab Hamden, CT Associate Scientist, Central Laboratory Services B.S. in Physiological Science, Epidemiology, Microbiology, Immunology, Genetics, Biology, Molecular Biology, Cell Biology, Biotechnology, Biochemistry Exp: Entry Level |
NOTE: PLEASE SUBMIT BOTH RESUME AND COVER LETTER TO APPLY FOR THIS JOB. KINDLY DISCUSS YOUR MOTIVATION, RELEVANT EXPERIENCE, SALARY REQUIREMENTS, AND VISA STATUS IN YOUR SUBMISSION. If interested, please e-mail your resume to careers@nebiolab.com. Gain an overall understanding of drug development and maintenance of the full chain of sample custody for regulatory compliance Support implementation of Laboratory Information management System (Watson LIMS) for sample management and storage Sample management and reconciliation, kit preparation and verification, and document preparation related to biological sample collection, storage, and shipment for clinical trials Streamline inventory management, consumable ordering, and other documentation requests for Quality Assurance Unit Help maintain ultra-low temperature (ULT) freezers and refrigerators and associated electronic logs and records Learn bioanalytical techniques for the analysis of drug and biomarkers in biological matrices Follow appropriate safety and study requirements by reading, understanding, and following Standard Operating Procedures (SOP), Good Laboratory Practices (GLP) requirements, and Sponsor Study protocols Support business development and marketing activities, foster client relationships, and help onboard new sponsors | 9/21/2023 |
| 3999 | Nephron Pharmaceuticals West Columbia, SC Microbiology Quality Specialist Bachelor’s degree Exp: 1 year |
Position Summary: Responsible for timely review of laboratory data, Standard Operating Procedures (SOPs), Equipment Validations, studies, and other documents related to the Microbiology department, as needed. Creates and executes project review plans; ensures timely completion of studies or assigned special projects to meet changing needs, requirements, and deadlines of the Microbiology department. Assists with additional work duties or responsibilities as evident or required | 9/21/2023 |
| 4000 | Nephron Pharmaceuticals West Columbia, SC Microbiology Quality Investigator Bachelor’s degree preferred. Exp: 1-2 years |
Position Summary: Assures compliance with FDA regulations in the areas of non-conformance investigations, memorandums, deviations, and corrective and preventive actions (CAPA’s) for the Environmental Monitoring (EM) department. Works effectively with other departments to ensure timely completion of projects, as well as effective management of individual workloads. Performs other duties as assigned or apparent. | 9/21/2023 |
| 4001 | Nephron Pharmaceuticals West Columbia, SC Microbiology R&D Analyst I · Regionally accredited Master’s Degree in Microbiology or other science-related field. Exp: 1 - 3 years |
Position Summary: Performs research and develops projects for both established and new products, including, but not limited to, microbiological test method validation/transfer/verification, procedures, investigations, and other non-specified projects or initiatives. Plans, organizes, and manages resources on method validation projects to assure technical quality and schedule adherence. Performs other duties as assigned or apparent. Works with different microbiological techniques and equipment, including but not limited to gram stain, turbidimetric endotoxin testing, liquid particle counter, isolator, bioburden, filtration analysis, sterility testing, aseptic process simulation, and MALDI-TOF. Performs different microbiological tests for R&D Microbiology and QC Microbiology, as needed; also understands and performs routine investigations related to Environmental Monitoring and laboratory testing. Works in a GMP environment and responsible for generating cGMP data. Plans and executes research and test method development projects for both established and new products. Participates in development and implementation of associated programs (e.g. cleaning validation, process validation, cGMP compliance, equipment validation, maintenance and use, etc.), as well as generating trending reports for cleanroom environments. Participates in reading and documenting media fill results. Works in a cGMP environment and is responsible for generating cGMP data. Ensures reports, submission documentation, and development summaries documenting the product development process are available for clients, partners, and health authorities (i.e. FDA). Assists in drafting R&D and QC protocols, summary reports, and studies. | 9/21/2023 |
| 4002 | Nephron Pharmaceuticals West Columbia, SC Analytical Chemist I - Second Shift (Sun. - Thurs. - 2:00pm to 11:00pm) BS or MS in Chemistry, Biochemistry or a related field required. Exp: 0-3 years |
Position Summary: • Support quality control testing and research and development activities as needed. • Assists with additional work duties or responsibilities as evident or required. • Performs other duties as assigned or apparent. • Relies on instructions and pre-established guidelines to perform job functions. • Works under immediate supervision. • Relies on instructions and pre-established guidelines to perform job functions. • Works under immediate supervision. | 9/21/2023 |
| 4003 | Nephron Pharmaceuticals West Columbia, SC Analytical Chemist I - First Shift (Mon. - Fri. - 8:00am to 5:00pm) BS or MS in Chemistry, Biochemistry or a related field required. Exp: 0-3 years |
Position Summary: • Support quality control testing and research and development activities as needed. • Assists with additional work duties or responsibilities as evident or required. • Performs other duties as assigned or apparent. • Relies on instructions and pre-established guidelines to perform job functions. • Works under immediate supervision. | |
| 4004 | Nexcelom Bioscience San Diego, CA Research Associate I - Protein Purification Bachelor’s Degree in biological sciences. Exp: 0 - 1 year |
This position is responsible for developing recombinant protein research products in the Molecular Cellular Biology group by using cutting-edge synthetic biological technology. The duties include preparing buffer solutions and E. Coli cell culture media, performing bacterial cell cultures, and purifying recombinant proteins with affinity tag, performing protein characterization according to standard operating procedures. This position offers a significant opportunity for learning molecular biology techniques and career growth in the biotechnology industry. | 9/22/2023 |
| 4005 | Nexcelom Bioscience Pittsburgh, PA Associate Specimen Processor Associate or Bachelor's degree in a life sciences discipline. Exp: 0-1 year |
KEY RESPONSIBILITIES Receive and process clinical samples within the guidelines of the site working procedures. Enter data into laboratory information systems. Split down and remove excess packaging to reduce waste footprint within the building. Transfer from and to internal lab areas in a timely manner. Demonstrate thorough knowledge of accessioning processes and quality control. Ensure Good Documentation Practices (GDP) are followed, including proper specimen handling, labelling and preparation of required documents. Other duties as assigned by Supervisor | 9/22/2023 |
| 4006 | Nexcelom Bioscience Boston, MA Associate Chemist B.S. degree in a Life Sciences field. Exp: 0-4 years |
We are seeking a bachelor's level candidate to join a team of scientists manufacturing synthetic chemical products used throughout the world in scientific research applications. This position will function as a member of the production staff and will participate in the transfer, implementation and on-going production of products in the laboratory. | 9/22/2023 |
| 4007 | Nexcelom Bioscience Lafayette, CO Associate Scientist Bachelor's Degree in Life Sciences. Exp: 0-3 years |
This is a 2nd shift position- 4-day work week– Monday-Thursday 12pm-10:30pmMT. Job Summary: Revvity has a rewarding and exciting opportunity for an Associate Scientist for our Synthetic Manufacturing laboratory. The Associate Scientist position will perform primary tasks in an ISO 9001:2015 laboratory in Lafayette, CO. Key responsibilities for this position include a wide array of duties related to the manufacturing, processing, and packaging of RNA and DNA oligonucleotides. This includes synthesis, cleaving, quality and quantity determination, purification, inventory control, and order packaging. The position will require the ability to learn and to troubleshoot various aspects of manufacturing chemistry in multiple laboratories. | 9/22/2023 |
| 4008 | Nexcelom Bioscience San Diego, CA Research Associate II - Product Development (Cell Analysis) Bachelor or Master’s degree in a Life Science related field. Exp: 1+ years |
BioLegend is seeking a self-motivated Research Associate to join our Product Development team in San Diego. The incumbent will actively participate in all the stages of the development, optimization, and validation of new products. This position will have the opportunity to interact with multi-disciplinary teams. The work requires routinely handling small animals and biological samples from animals and human donors. Prior experience in tissue culture, flow cytometry, immunoassays, molecular biology techniques (eg PCR, cloning, etc), data analysis, and project management are preferred | 9/22/2023 |
| 4009 | Northstar Medical Technologies Beloit, WI Manufacturing Engineer Bachelor’s Degree in Engineering Exp: 0+ years |
The Manufacturing Engineer is responsible for evaluating manufacturing processes by assisting in the design and conduction of research programs; applying knowledge of product design, fabrication, assembly, tooling/equipment, and materials. This position will assist in coordinating product and process improvements to meet quality and production goals. All duties and responsibilities will be done in compliance with cGMP and FDA regulations. | 9/22/2023 |
| 4010 | Nostrum Laboratories Kansas City, MO Chemist I Bachelors Degree in Chemistry, Pharmaceutical, Biology or a science related field. Exp: 0+ years |
General Summary Description The Chemist I is responsible for developing and validating test methods; validating laboratory instruments; conducting lab testing for raw materials, components, in-process materials, finished products, stability, and other samples in accordance with cGMP regulations, regulatory filings, and approved procedures. | 9/22/2023 |
| 4011 | Nostrum Laboratories Bryan, OH Chemist I Bachelors Degree. Masters Degree or PhD. preferred. Exp: BS: 0 - 4 years; MS or PhD: 0 - 2 years |
General Summary Description Responsible for development and validation of analytical methods in support of product development and IND/NDA/ANDA filings. Perform routine wet chemical and instrumental analysis on raw materials, in-process, finished and stability products. Accurately compiles and reports data. Gather, compile and compose documents needed for regulatory submissions | 9/22/2023 |
| 4012 | Nostrum Laboratories Bryan, OH MICROBIOLOGIST I Bachelors Degree in Biology or Microbiology. Exp: 0+ years |
Perform all testing on in-house and contract samples as needed: o In-process o Finished product o Stability o Raw material (including water) o Environmental Testing | 9/22/2023 |
| 4013 | Nostrum Laboratories Bryan, OH METROLOGIST I Bachelors Degree in Chemistry or Physical Science. Exp: 1 - 2 years |
Duties and Responsibilities Develops calibration methods and techniques based on principles of measurement science, technical analysis of measurement problems, and accuracy and precision requirements Identifies magnitude of error sources that contribute to uncertainty of results to determine reliability of measurement process in quantitative terms Calibrates/qualifies a variety of process laboratory equipment, measurement/control instrumentation, and software Conducts daily calibration check as needed Schedule and perform calibrations according to SOPs or manufactures procedures on Measurement and Test Equipment insuring schedule work requirements are met Completes all calibration certificates Ensures accuracy, reliability, and compliance with operating procedures Performs data entry functions required to update the calibration database, as required Initiates instrument/document change control as necessary Maintains documentation according to SOPs and cGMP requirements Writes, develops, and reviews Standard Operating Procedures | 9/22/2023 |
| 4014 | Nova Biomedical Waltham, MA Associate Scientist B.S./ B.A. Degree in Chemistry, Biology, Biomedical engineering or related field Exp: 0-2 years |
Nova Biomedical is looking for an Associate Scientist to join our Organic Research Lab in Waltham, MA. In this role, you will work within a multi-disciplinary team to conduct the research and development of chemical/biological sensors, assays, and reagents for the clinical analyzers and instrumentations | 9/22/2023 |
| 4015 | Nova Biomedical Waltham, MA Quality Engineer I Undergraduate Degree with a concentration in the sciences. Exp: I -2 years |
Nova Biomedical is hiring a Quality Engineer to be responsible for testing and ensuring the quality of all products manufactured by Nova Biomedical in the Waltham, MA facility. You will manage the qualification of processes and equipment, ensuring that all processes are performed according to established procedures and working with Research and Development and Manufacturing Engineering to remedy issues encountered. You will ensure that Quality Systems practices are an integral part of planning, production, and analytical activities using engineering, scientific, and technical principles. | 9/22/2023 |
| 4016 | Nova Biomedical Waltham, MA Supplier Quality Engineer BS degree in an Engineering discipline. Exp: I year |
Nova Biomedical is hiring a Supplier Quality Engineer in our Waltham, MA office to support programs to qualify suppliers and improve supplier performance and productivity. More specific responsibilities include: Support the ongoing maintenance of the Approved Suppliers List (ASL) through the following activities: Updating the contents of the ASL as required, and as directed. Support the initial evaluation for new suppliers. Support the qualification activities for high-risk suppliers by participating in remote and onsite supplier audits. Requalify existing suppliers by performing desktop surveillance audits. Maintain all supplier qualification-related documentation. Generate periodic supplier performance reports and provide them to suppliers. Support the Nova Supplier Change Notification (SCN) process. Initiate SCNs as the result of having received a supplier-generated Product Change Notification (PCN) or other supplier generated notification of a required change. Manage the SCN database. Support the disposition of Nonconforming Material Reports (NCMR) and issuing Supplier Corrective Action Requests (SCAR) as directed. Maintenance activities för the NCMR, SCAR, and SCN databases. | 9/22/2023 |
| 4017 | Novartis Cambridge, MA Research Scientist / Senior Scientist, Preclinical Safety, Pathology, Immunology – Dual Posting Research Scientist: Education: bachelor’s or master’s degree or equivalent in immunology, cell biology or Medicine. Exp: 0-5 years |
We are seeking to hire a motivated candidate with a strong background in cellular and molecular immunology to join our Immunology Group in Cambridge, MA. The candidate will support cross-species in vivo and in vitro immunology testing using preclinical models, including non-human primates, towards non-clinical safety assessment and to address key scientific questions on comparative biological responses to novel medicines, bridge gaps in translational immunology and explore hematopoietic system physiology. You’ll also have continuous opportunity to work with other Novartis experts in flow cytometry, immunology, and related scientific and technical areas to expand your learnings. Ultimately, you will improve and accelerate Novartis drug discovery and development processes aimed to bring forward effective and safe medicines. | 9/22/2023 |
| 4018 | Novartis Cambridge, MA Research Scientist Biochemistry, CVM BS or MS degree in biochemistry, molecular biology, cell biology, biophysics, biomedical engineering, or a related field. Exp: 1+ years |
We are seeking a highly motivated in vitro Research Scientist to join our Biochemistry team. Here you will advance our understanding of disease biology and the discovery of new drugs, by contributing to target validation, assay development and drug screening efforts throughout the disease area and in collaboration with the larger research organization. As a biochemistry and cell biology Research Scientist, you will conduct experiments both independently and collaboratively in an inter-disciplinary setting to support drug discovery projects | 9/22/2023 |
| 4019 | Novavax Gaithersburg, MD Research Associate II, Formulation Development Bachelor degree or a Master degree in a formulation development relevant field. Exp: 1 to 2 year |
Responsibilities include but are not limited to: Perform rapid, comprehensive characterization of candidate drug products to determine the physicochemical properties of the drug product and evaluate them for further drug development programs including: AUC, CD, Fluorescence spectroscopy, DSC, ITC, UV/Vis spectroscopy, FTIR, SLS and HPLC. Percentage of time (Approx): 65% Assist in the development and scale-up of drug product processes from bench top to pilot scale and technology transfers. Percentage of time (Approx): 10% Provide support to formulate small and large scale lots of liquid, frozen or lyophilized drug substance/product samples. Percentage of time (Approx): 5% Assist in development of formulation studies and design protocols. Percentage of time (Approx): 5% Project management of other research associates in support of the larger drug development project. Percentage of time (Approx): 5% Write technical reports and applicable SOPs. Percentage of time (Approx): 5% Responsible for preparing data summary presentations, compiling data and authorizing technical reports. Percentage of time (Approx): 5% | 9/22/2023 |
| 4020 | Novavax Gaithersburg, MD Associate II, Analytical Development Bachelor’s degree OR Master’s degree. Exp: BS:1-2 years; MS: 0-1 year |
Novavax is seeking an Associate II, Analytical Development to provide technical and documentation support in a laboratory setting. This role is responsible for contributing to the method development, qualification, and technology transfer for analytical methods. The qualified individual will bring experience in relevant analytical technologies, such as ELISA, VaxArray, Luminex, or BLI. The position will perform in-process testing, as needed, to support the Process Development, Formulation Development, and Manufacturing teams, in addition to method development and qualification. This position will report to the Sr. Scientist, Analytical Development. | 9/22/2023 |
| 4021 | Novo Nordisk Lexington, MA Research Associate - ADME B.S./M.S. in a scientific discipline, analytical chemistry, chemistry, biochemistry, biotechnology or related discipline preferred. Exp: 0+ years |
We are seeking a Research Associate - Absorption, Distribution, Metabolism and Excretion to help support the development of our growing pipeline of product candidates. The individual in this position will assist in the conduct of nonclinical studies and the ADME assays and sample analysis. | 9/22/2023 |
| 4022 | Novo Nordisk Clayton, NC Associate Process Engineer - Site Capacity bachelor’s degree within engineering or natural sciences, manufacturing or similar which could be as mechanical engineer, process engineer, consultant Exp: 0-3 years |
Fill-Finish Expansion is seeking a Robotic Engineer for the Material Handling Work-Package. In this role, you will play a crucial role in creating future standards for equipment that handles incoming materials for filling lines and transforming existing manual processes into fully automated ones. As a Robotic Engineer, you will leverage your expertise in automation to collaborate with us and future vendors in developing, designing, and producing the solutions Novo Nordisk needs for future facilities worldwide. To succeed, you must bring relevant automated material handling and/or robotics experience, harvest the existing knowledge of the company, and combine the inputs into state-of-the-art material handling technology solutions while working with local and global stakeholders. Your overall objective is to conceive and develop robotic solutions to optimize our manufacturing through traditional automation and robotics. | 9/22/2023 |
| 4023 | Novo Nordisk Fremont, CA Engineer I Bachelor’s degree Exp: 0- 1+ years’ |
The Engineer I will make significant contributions to the research of life changing medical devices at Novo Nordisk (NN). They leverage their strong background in engineering to perform their individual tasks as well as energetically engaging in collaborative work. The Engineer I will contribute to insert subject matter expertise. They ensure strong progress on research initiatives under the broad direction of more senior engineers and management. | 9/22/2023 |
| 4024 | Noxilizer Hanover, MD Research and Development Laboratory Scientist Bachelor’s degree in Biology, Biotechnology, Biomedical Engineer, Material Science or related field preferred. Exp: 1 year |
The R&D Lab Scientist is responsible for performing, documenting and reporting microbiological sterilization studies for Noxilizer’s customers. Noxilizer’s customers range from Fortune 500 pharmaceutical, biotech and medical device companies to start-ups that are in the US, Europe and Asia. These studies are the first critical step in the customer’s evaluation of nitrogen dioxide sterilization and their product, as well as an important revenue-generating area for the company. The R&D Laboratory Scientist will join a high-performing team of experts to solve sterilization challenges while they grow their skills for future career opportunities. | 9/22/2023 |
| 4025 | Nucelis San Diego, CA Research Associate, Analytical Chemistry BS/BA or MS in Chemistry or related scientific discipline. Exp: 1+ years |
We are seeking a highly capable and energetic analytical research associate (RA or Senior RA) that is willing to work as part of a team to isolate, identify, quantify, and characterize natural products from our engineered systems. This role will require routine execution of established analytical protocols and the ability to work independently as we support company-wide research projects in the analysis of plant and fermentation analytes. The ideal candidate will have hands-on experience with analytical instrumentation (GC/MS, LC/MS, HPLC) and experience with natural product identification, quantification, and characterization and/or have a desire to gain significant experience in these areas. | 9/22/2023 |
| 4026 | Nutcracker Therapeutics Emeryville, CA Research Associate/Sr. Research Associate, Analytical Development (Contract) Bachelor’s or Master’s degree in a relevant field, e.g. Biochemistry, Molecular Biology, Chemistry, Bioengineering Exp: one year |
We are looking for a talented RA/SRA (contract) to join the Analytical Development team in support of process and product characterization. This individual is a motivated self-starter who thrives by generating high-quality data in the laboratory. The ideal candidate is also looking for a challenging work environment that provides opportunities for collaboration and growth. If you are driven to discover, create, and inspire something that moves science and technology forward, and lasts a lifetime and beyond, you’re ready to be a Nutcracker. This is a contract position lasted an expected 6 months | 9/22/2023 |
| 4027 | Nvigen Campbell, CA Laboratory Technician Bachelor’s degree in chemistry or biology preferred. Exp: 0+ years |
Familiar with standard chemical or molecular laboratory techniques and practices. Primary responsibilities will include assisting researchers with sample processing, assay evaluation and improvement. Must be able to follow detailed protocols with minimal supervision. Successful candidate will be highly motivated, eager to learn, and be able to meet the challenges of a fast-paced environment. Must possess excellent attention to detail, be organized and can maintain detailed records. Must have good communication skills and be able to work effectively independently and in a team. Support general lab management duties such as ordering supplies, maintaining equipment and organization. Prior experience in biological or chemical laboratory required. | 9/22/2023 |
| 4028 | Ocean Ridge Biosciences Concord, OH Laboratory Technician - Genetic Toxicology Bachelor’s degree in biology, microbiology, chemistry, or a related field. Exp: 1+ years |
We are currently seeking a Lab Technician to join our team and provide technical support for performing standard genetic toxicology assays. This position will play a crucial role in our laboratory operations, which include various cell-based assays, bacterial reverse mutation assay, rodent bone marrow and blood based micronucleus assays, and other related in vitro activities. | 9/22/2023 |
| 4029 | Ocean Ridge Biosciences Chicago, IL Assistant/Associate Toxicologist BS degree in animal/veterinary science, biology, or related disciplines. AALAS accreditation is a plus. Exp: Associate Toxicologist: 0-3 years |
Position/Job Summary: The Associate/Assistant Toxicologist plays a key, hands on role in the conduct of preclinical studies and supports the Study Director to ensure that Sponsor studies are conducted properly and according to FDA guidelines. | 9/22/2023 |
| 4030 | Ocean Ridge Biosciences Hayward, CA Research Assistant - Bioanalytical Services B.S. degree in related scientific discipline. Exp: 0-3 years |
Job Summary 1) Assist lab work and method development 2) Follow SOP and protocol to conduct method validation and sample analysis under supervision 3) Comply with GLP regulations in lab work and documentation 4) QC review data and reports 5) Perform instrument setup, maintenance, and basic trouble-shooting under supervision 6) Strictly follow SOPs and regulations to serve as sample coordinator. | 9/22/2023 |
| 4031 | Olympus Indianapolis, IN Field Service Engineer I (Indianapolis, IN) Associate degree in electronics, computer science or related technical discipline is required or equivalent Military Technical Training. Bachelor’s de Exp: one to three years |
Job Description The Field Service Engineer (FSE) services and maintains all product lines for Olympus America medical products. Under supervision of Manager and Senior FSE Trainer, the FSE will service and provide expert level technical support to assigned equipment. | 9/22/2023 |
| 4032 | Olympus Orlando, FL Field Service Engineer I (Florida, Orlando) Associate degree in electronics, computer science or related technical discipline is required or equivalent Military Technical Training. Bachelor’s de Exp: one to three years |
Job Description The Field Service Engineer (FSE) services and maintains all product lines for Olympus America medical products. Under supervision of Manager and Senior FSE Trainer, the FSE will service and provide expert level technical support to assigned equipment. | 9/22/2023 |
| 4033 | Olympus San Antonio & Austin, TX Field Service Engineer I (Texas) Associate degree in electronics, computer science or related technical discipline is required or equivalent Military Technical Training. Bachelor’s de Exp: one to three years |
Job Description The Field Service Engineer (FSE) services and maintains all product lines for Olympus America medical products. Under supervision of Manager and Senior FSE Trainer, the FSE will service and provide expert level technical support to assigned equipment. | 9/22/2023 |
| 4034 | Olympus New York City, NY Field Service Engineer Associate degree in electronics, computer science or related technical discipline is required or equivalent Military Technical Training. Bachelor’s de Exp: one to three years |
Job Description The Field Service Engineer (FSE) services and maintains all product lines for Olympus America medical products. Under supervision of Manager and Senior FSE Trainer, the FSE will service and provide expert level technical support to assigned equipment. | 9/22/2023 |
| 4035 | Olympus Boston, MA Field Service Engineer I (Boston, MA) Associate degree in electronics, computer science or related technical discipline is required or equivalent Military Technical Training. Bachelor’s de Exp: one to three years |
Job Description The Field Service Engineer (FSE) services and maintains all product lines for Olympus America medical products. Under supervision of Manager and Senior FSE Trainer, the FSE will service and provide expert level technical support to assigned equipment. | 9/22/2023 |
| 4036 | Olympus Cincinnati, OH Field Service Engineer I (Cincinnati, Ohio) Associate degree in electronics, computer science or related technical discipline is required or equivalent Military Technical Training. Bachelor’s de Exp: one to three years |
Job Description The Field Service Engineer (FSE) services and maintains all product lines for Olympus America medical products. Under supervision of Manager and Senior FSE Trainer, the FSE will service and provide expert level technical support to assigned equipment. | 9/22/2023 |
| 4037 | Olympus San Jose, CA QA Engineer I Bachelor’s Degree in Engineering or Scientific Discipline (or equivalent). Exp: 0-2 years |
Job Description The Quality Assurance Engineer I is responsible for providing Quality Engineering input to support Production, Operations and Engineering activities. Maintains and follows Quality Engineering methodologies, systems, and practices which meet Olympus, customer, and regulatory requirements. Serves as a Quality representative to improve awareness, visibility and communication on Quality initiatives to support departmental, functional, site, divisional and corporate Quality goals and priorities. When needed, works with Olympus Tokyo representatives/liaisons to resolve Quality related issues. | 9/22/2023 |
| 4038 | Lonza Portsmouth, NH Biotech Nights Manufacturing (Entry and Junior Level Positions) AS/BS preferred; Science related discipline Exp: 1+ years |
This posting is for candidates interested and willing to work night shifts: The night shift schedule is from 7pm-7am, on a rotational schedule every other week: Week 1: M/T/F/SAT/SUN Week 2: W/TH Shift differentials are included for weekends and nights worked Are you seeking to kickstart your career in the manufacturing or life sciences industry? Or perhaps you already have some experience and are looking for the next challenge? We have openings for entry to junior level manufacturing associate positions here at Lonza in Portsmouth NH. If you're detail oriented, motivated, and eager to learn, this could be the perfect role for you! Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. The Manufacturing Associate I is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP) conditions. Level I associates are expected to execute process recipes, follow written Standard Operating Procedures (SOPs), monitor equipment and processes, independently perform laboratory tasks, including pH, conductivity testing, product sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to demonstrate a strong understanding of cGMP compliance while operating under supervision, and aseptic technique in handling of products and materials. Level II Operators may also be asked to troubleshoot equipment events, initiate deviations, review batch records and logbooks. | 9/14/2023 |
| 4039 | Lonza Portsmouth, NH Biotechnologist Level 1 (Nights) AS/BS preferred; Science related discipline Exp: 1+ years |
The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP) conditions. Level I associates are expected to execute process recipes, follow written Standard Operating Procedures (SOPs), monitor equipment and processes, independently perform laboratory tasks, including pH, conductivity testing, product sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to demonstrate a strong understanding of cGMP compliance while operating under supervision, and aseptic technique in handling of products and materials. Level II Operators may also be asked to troubleshoot equipment events, initiate deviations, review batch records and logbooks. Level III associates are expected to be SMEs on all core functions in the suite with anticipated cross training into other manufacturing areas within the asset. Senior associates are expected to be expert within operations and lead the manufacturing team from a technical perspective. Senior associates are expected to be proficient in trouble shooting, appropriate escalations and are able to facilitate a path forward to maintain safety and quality for the product. Shift Schedule: The shift schedule is from 7pm-7am, on a rotational schedule every other week: Week 1: M/T/F/SAT/SUN Week 2: W/TH Shift differentials are included for weekends and nights worked Initial 2 week training period on day shift Monday-Friday upon hire | 9/14/2023 |
| 4040 | Lonza Portsmouth, NH Biotechnologist II (A Shift Days) AS/BS preferred; Science related discipline Exp: 1+ years |
Shift Schedule: The shift schedule is from 7am-7pm, on a rotational schedule every other week: Week 1: M/T/F/SAT/SUN Week 2: W/TH Shift differentials are included for weekends and nights worked Initial 2 week training period on day shift Monday-Friday upon hire for new hires The Manufacturing Associate I is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP) conditions. Level I associates are expected to execute process recipes, follow written Standard Operating Procedures (SOPs), monitor equipment and processes, independently perform laboratory tasks, including pH, conductivity testing, product sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to demonstrate a strong understanding of cGMP compliance while operating under supervision, and aseptic technique in handling of products and materials. Level II Operators may also be asked to troubleshoot equipment events, initiate deviations, review batch records and logbooks.Shift Schedule: The shift schedule is from 7am-7pm, on a rotational schedule every other week: Week 1: M/T/F/SAT/SUN Week 2: W/TH Shift differentials are included for weekends and nights worked Initial 2 week training period on day shift Monday-Friday upon hire for new hires | 9/14/2023 |
| 4041 | Lonza Houston, TX Core Technician - Viral Vector / Cell Therapy Bachelor’s or Associate’s Degree in Life Sciences Exp: 1+ years |
Lonza Cell and Gene Therapy is the largest in the world and our Houston, TX site is growing. As a Core Technician in Viral Vector or Cell Therapy, you will be working at, and learning from, one of the industry leaders. We are world-class manufacturing experts, who strive for continuous improvements in environments where change is constant. You will be part of a team, performing a variety of tasks involved in the production of sterile biological pharmaceutical products and collaborating closely with your colleagues to deliver innovative processes. As we run a 24/7/365 operation, roles may include working a variety of shifts, including nights and weekends. | 9/14/2023 |
| 4042 | Loxo Oncology San Diego, CA Contract Scientist/Senior Scientist (Non-PhD), Protein Expression MS in protein sciences, biology, biochemistry, molecular biology, life sciences or a related field. Exp: 1+ years |
This Contract position offers the opportunity to be part of Loxo@Lilly’s discovery teams focused on creating novel, highly specific and selective drugs for genetically identified targets. The Contract, Protein Scientist will support the internal and external discovery research efforts across multiple projects and project teams. This is an extremely important role where the right person will be able to have a real impact on cutting-edge science, making a real difference in patient’s lives | 9/15/2023 |
| 4043 | LSI Solutions Victor, NY Process Validation Engineer Process Validation Engineer I: Bachelor’s Degree in an engineering, technical or manufacturing discipline. Exp: 1-3 years' |
The Process Validation Engineer will develop and execute validations to ensure regulatory compliance to established internal and external standards related to released product or current production. The individual will support the writing of validation protocols and reports, along with the gathering and analysis of data. | 9/15/2023 |
| 4044 | LSI Solutions Victor, NY Product Design Engineer Product Design Engineer I: Bachelor’s Degree or higher in Engineering or related technical discipline required. Exp: 0-3 years |
Supports introduction of new products by leading and maintaining all Product Engineering related activities. Senior Product Design Engineer provides functional expertise, leadership, and mentorship to the Product Engineering function. | 9/15/2023 |
| 4045 | LSI Solutions Victor, NY Manufacturing Engineer - Days (8am to 5pm) Level I: BS Engineering or Engineering Tech. Exp: 0-3 years |
The Manufacturing Engineer under R&D is responsible for leading the development, selection, and transfer of manufacturing processes during New Product Development (NPD) projects. This role supports equipment qualification and process validation activities as well handling development of workflows, assembly methods, and risk assessment tools to define a process that meets the project requirements. | 9/15/2023 |
| 4046 | LSI Solutions Victor, NY Manufacturing Engineer II (Days) Level II: MS Engineering Exp: 1 to 5 years |
The Manufacturing Engineer is responsible for manufacturing process performance, receiving new products transfer into series production, product and problem diagnosis and repair. Support the development, qualification, verification, and validation of changes to existing product and manufacturing processes. Maximizes efficiency by analyzing equipment layouts, workflow, assembly methods, and work force and equipment utilization. Develop short- and long-term operational strategies in partnership with senior team members and provide the leadership necessary for the successful design, development, and execution of that strategy to achieve measurable outcomes in a timely, cost-effective manner. | 9/15/2023 |
| 4047 | LSI Solutions Victor, NY Regulatory Associate - Days 8am to 5pm Regulatory Associate I: Bachelor or Master’s degree in a technical, regulatory, or life sciences discipline Exp: RAI: 0-2 years’ ; RAII: 1-2 years’ |
The Regulatory Associate applies her/his experience, knowledge, organization skills, and communication skills in a wide variety of tasks. All Regulatory Associates provide regulatory feedback and guidance based on medical device regulations and standards to the company throughout the development cycle. Regulatory Associates monitor regulations, standards, policies, and guidance for new and current compliance requirements that may have impact to the company. Regulatory Associates maintain technical documentation and help to implement change control at LSI. Regulatory Associates are assigned to work in one or more of the following areas: Domestic, European, Rest of World, Labeling, and/or Clinical & Post Market Surveillance. Regulatory Associates assigned to Domestic projects will contribute to regulatory strategies for design and development projects and contribute to regulatory submissions to the FDA when appropriate. Regulatory Associates assigned to European regulatory projects will be involved with medical device classification, preparation of technical documentation, conformity assessments, and notices of change in compliance with the EU MDR and associated guidance. Regulatory Associates assigned to Rest of World projects will work with distributors to provide documents for regulatory submissions required to market LSI’s new or modified medical devices in many countries outside the U.S and Europe. Regulatory Associates assigned to Labeling projects apply knowledge of U.S. and international regulations and standards with highly cross-functional teams to ensure compliance for IFU, UDI, and promotional material requirements. Regulatory Associates assigned to Clinical projects contribute to clinical evaluation, investigator brochures, post-market clinical follow-up, and post market surveillance. All Regulatory Associates will also maintain full Quality and Regulatory compliance with all standards that govern the design, development, manufacturing, and distribution of our medical devices. | 9/15/2023 |
| 4048 | Lumen Bioscience Seattle, WA Lab Technician BA/BS degree in molecular biology, biochemistry, biotechnology, microbiology or related field of study. Exp: 1-2 years |
Lumen is seeking a highly motivated and detail-oriented Laboratory Technician to join our team. The Laboratory Technician will closely work with other scientists in the R&D group to develop biologics using Lumen’s spirulina-based expression system. The individual is expected to handle and maintain cyanobacterial cultures; perform standard molecular biology techniques such as PCR, bacterial cloning, bacterial transformation, plasmid purification and gel extraction; and contribute to general lab housekeeping. The position requires the ability to work independently with minimal supervision as well as within a team. It also requires significant attention to detail and the ability to track a large amount of processes and samples occurring in parallel. A successful candidate should also be comfortable assisting other laboratory personnel in the development and application of new techniques. The position requires the ability to work as a team member in a fast-paced environment and to assist other laboratory personnel as needed. It is central to Lumen’s acquisition and integration of new and complex technologies, and to sharing such capabilities with other teams, and as such, flexibility and independence will be essential. The position requires strong organizational skills and meticulous laboratory record keeping. Effective communication skills are crucial in coordinating with the relevant teams to meet milestones and deadlines and in raising quality or troubleshooting issues as they may arise. The position includes providing status updates and presenting in group and company-wide meetings. | 9/15/2023 |
| 4049 | Lung Biotechnology Manchester, NH Research Associate I/II - Cell Production & Process Development Master’s Degree in cellular biology, developmental biology, biomedical engineering or related field Exp: 1+ years |
The Research Associate II – Cell production and Process Development will perform and contribute to the design of cell studies as well as execute analytical methods to support the production and process development of iPS-derived cells and cellularized 3D scaffolds for the development of autologous 3D printed tissue engineered organs. | 9/15/2023 |
| 4050 | Lung Biotechnology Manchester, NH Research Associate II - Tissue Systems Master’s Degree in cell biology, biomedical engineering or related field Exp: 1+ years |
The Organ Manufacturing group (OMG) at Lung Biotechnology focuses on identifying, scoping, and delivering projects in support of our mission to build cutting edge technology for organ scaffold 3D bioprinting to address the unmet needs for transplantable organs. The Research Associate II-Tissue Systems will work with the direct supervisor to establish new experimental procedures and analytical metrics to characterize the biological outcomes of different lung cell types on 3D printed lung scaffolds. | 9/15/2023 |
| 4051 | Lykan Bioscience Hopkinton, MA QC Analyst, Microbiology Bachelor's degree in scientific discipline preferred. Exp: 0-2+ years' |
The Quality Control Analyst, Microbiology will be responsible for collection of environmental and raw material samples, sample management activities, and testing of cell therapy in-process, release and stability product samples. He/she will be responsible for reporting of data and writing/revising standard operating procedures (SOPs). He/she may support equipment onboarding and qualification as well as test method qualification in compliance with all applicable quality systems and current cGMPs. Identifies and supports initiation and completion of deviations, corrective and preventative actions, and laboratory investigations in compliance with all applicable quality systems and current cGMPs. | 9/15/2023 |
| 4052 | Marker Therapeutics Houston, TX Cell Therapy Manufacturing Technician BS, MS in Biology or a related science Exp: 1-5+ years |
Marker Therapeutics is seeking a cell therapy technician for its manufacturing group to support its ongoing efforts to develop immunotherapies for the benefit of patients with cancer. This position will work under the guidance of the Senior Director of CMC and perform assigned responsibilities to support the company’s product manufacturing process and process improvement initiatives. Depending on previous experience and qualifications, this individual will be expected to either lead or support the manufacturing process and process characterization of scale-up/scale-down cell manufacturing processes, including optimizing process parameters, cell concentrations and therapeutic product fill and finish technologies to advance our therapeutic programs. The successful candidate must be a team player with strong expertise in GMP manufacturing and must have the ability to communicate and collaborate within an interdisciplinary environment. | 9/15/2023 |
| 4053 | Maverick Therapeutics Social Circle, GA Filling and Packaging Engineer I Bachelor’s degree in Engineering discipline required. Exp: 1+ years |
The Filling and Packaging Engineer, reports to a Production Manager and is responsible for on-shift operational support of the IG department in Covington, GA. The Filling and Packaging Engineer focuses on rapidly resolving manufacturing problems, enabling manufacturing to meet production goals. As a member of the operations team, you will provides on-shift technical knowledge and leadership. | 9/15/2023 |
| 4054 | Medpace Cincinnati, OH Biology Laboratory Technician Bachelor's degree. Exp: 1+ years |
Responsibilities Prepare samples according to project protocol and/or related SOPs; Maintain compliant laboratory documentation; Perform data analysis and data checking; Interpret results obtained for accuracy and acceptability; Clean and sterilize laboratory equipment; and Other duties deemed necessary. | 9/15/2023 |
| 4055 | Medpace Cincinnati, OH Chemistry Laboratory Technician Bachelor's degree. Exp: 1+ years |
Responsibilities Prepare samples according to project protocol and/or related SOPs; Maintain compliant laboratory documentation; Perform data analysis and data checking; Interpret results obtained for accuracy and acceptability; Clean and sterilize laboratory equipment; and Other duties deemed necessary. | 9/15/2023 |
| 4056 | Medtronic Danvers, MA Quality Engineer II Advanced Degree in Engineering, Science or technical field. Exp: 0+ years |
In this exciting role as a Quality Engineer II, you will have responsibility for the manufacturing transfer project(s) between sites which includes activities related to test method validation, process validation, design validation, inspection training, and process/quality change initiatives. This is an onsite role at the Danvers, MA location | 9/15/2023 |
| 4057 | Medtronic Brooklyn Park, MN Mechanical Design Engineer II Advanced Degree Mechanical Engineering. Exp: 0+ years |
Contribute to the development/sustainment of cardiac surgery disposable and capital goods products that meet application, business, customer, quality, and regulatory requirements. Such contribution includes collaborating with colleagues in Design, Research, Manufacturing, and Quality and preparing documentation, some of which may be submitted to regulatory agencies, in accordance with applicable procedures. | 9/15/2023 |
| 4058 | Medtronic Coon Rapids, MN Equipment Engineer II Advanced Degree Exp: 0+ years |
• Evaluates, selects and order equipment that is most appropriate and cost effective for the studies performed at PRL • Oversees the installation, upgrade and maintenance of equipment used in research operations, clinical lab, histology lab, necropsy areas, material characterization lab and biomaterials lab. • Maintain current records on equipment manufacturer’s technical notices, upgrades and safety issues. • Studies equipment performance and reliability • Establishes programs and solutions for increasing uptime and for equipment problems that affect the any PRL activity. • Provides technical support for the equipment repair. | 9/15/2023 |
| 4059 | Medtronic Littleton, MA Quality Engineer II - CST - Littleton, MA (Onsite) Advance degree in biomedical, Electrical, Computer, or Software engineering. Exp: 0 years |
We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives. Help us shape the future. | 9/15/2023 |
| 4060 | Merieux NutriSciences Columbus, OH Microbiologist 1 Bachelors preferred. Exp: One (1)- 2 years |
Purpose (Objective): The incumbent is responsible for the testing of samples using various microbiological analyses. The incumbent provides analytical support for the lab by ensuring that laboratory procedures are being performed within specified quality guidelines. This position serves as a technical resource and provides ongoing technical support related to method and process implementations. This position spends the majority of time or all of their time in diagnostics. | 9/15/2023 |
| 4061 | Merieux NutriSciences Crete, IL Chemist 1 Bachelors preferred. Exp: One - two years |
Purpose (Objective): The incumbent is responsible for performing chemical analysis on food/pharmaceutical samples. The incumbent analyzes the concentration of certain components in food samples. The incumbent must accurately prepare and process the samples to obtain the needed results. | 9/15/2023 |
| 4062 | Merieux NutriSciences Salt Lakre City, UT Chemist 1 Bachelors preferred. Exp: One - two years |
Analyses w/Extractions (Cholesterol, FAP, ICP, MOJO, FFA, etc.) Ensure that proper analysis methods are conducted on the appropriate samples. Maintain chemistry quality control records and procedures for each test. Extract desired components from samples with appropriate processes such as distillation, solvent extraction and acid digestion, so that concentrations can be determined. Calculate the concentration of components present in samples and post results. Wash glassware as needed and prepare samples as needed. Prepare standards or reagents that are needed for the analysis procedure. Maintain knowledge of Laboratory Information Management System (LIMS) required to complete job responsibilities. Maintain clean laboratory by washing countertops, sweeping floors, storing analysis materials, etc. | 9/15/2023 |
| 4063 | Meso Scale Discovery Rockville, MD Manufacturing Technician I Degree in Biology, Chemistry, Biotechnology, Engineering or related field is preferred. Exp: 1+ years |
Production role in consumables, kit or reagent manufacturing responsible for meeting production schedules in a fast-paced, high throughput industrial setting. This may include the production of coated plates, chemical buffers, and biological diluents/reagents and/or assembled kits for customer order fulfillment. Some degree of professional latitude, creativity and self-management is expected. | 9/15/2023 |
| 4064 | Moderna Therapeutics Norwood, MA Engineer II, Manufacturing Science & Technology MS Biochemical engineer, Chemical engineer, or Biochemistry background. Exp: 1 to 3 years’ |
This position is part of Moderna’s Manufacturing Science and Technology (MST) team responsible for ensuring the robust technology transfer and technical support of our mRNA platform in cGMP Manufacturing. The individual will work closely within MST, and with Process Development, Manufacturing, Regulatory, and Quality, to ensure all aspects of technology transfer and technical support are successfully executed. The individual may also provide engineering support like method writing for process equipment used at Moderna’s cGMP manufacturing operations in Norwood, MA. | 9/15/2023 |
| 4065 | Moderna Therapeutics Norwood, MA Research Associate, Drug Product Development Masters or Bachelor’s Degree in on one of the following fields: Chemical Engineering, Biochemical or Biomedical Engineering, Pharmaceutical Sciences, Exp: post Master’s Degree: 0 – 2 years; post Bachelor’s Degree: 0 – 4 years |
We are seeking a highly skilled and motivated Research Associate in Drug Product Development, to work in a team developing Moderna’s sterile drug product processes and products that enable clinical and future commercial supply. The primary role for this position will be to support product concept development including process development and scale-up work, container development and conditions of use studies. The incumbent will support the development of compositions, aseptic fill/finish unit operations through the development and use of scale-down models, process characterization studies etc. Applicants should have relevant pharmaceutical sciences related experience with various aspects of drug product development. The applicant should have exceptional ability to plan, execute and report, to communicate and collaborate, and requires strong attention to detail while working in a fast-paced, interdisciplinary environment. | 9/15/2023 |
| 4066 | Moderna Therapeutics Norwood, MA Engineer II, MS&T MS. Biochemical engineer, Chemical engineer, Biochemistry or Biology background. Exp: 1 to 3 years’ |
The Engineer II, MS&T will be part of Moderna’s Manufacturing Science and Technology team responsible for process implementation, technical support, and person-in-plant coverage to ensure the robust End-to-End production of our new mRNA Personalized Cancer Vaccine (PCV). The individual will work collaboratively with cross functional stakeholders such as Technical Development, Manufacturing, Regulatory, and Quality, to ensure all technical aspects of production are successfully executed. This will be a 2nd shift role and the individual will be working a Sunday through Wednesday schedule from 1:00pm until 11:00pm. | 9/15/2023 |
| 4067 | Moderna Therapeutics Norwood, MA Engineer II, Process Development Masters. Exp: 1-3 years |
The successful candidate must be able to work in a fast paced and highly dynamic environment, will have relevant academic and or industrial experience in drug delivery, process development or formulation development, and will be able to contribute to both process development and commercialization related activities. We seek applicants that are proactive, enthusiastic, and show a passion for their work. Applicants should have exceptional time management and communications skills with a strong attention to detail. Previous experience with chromatography, nanoparticle formulations, filtration technologies, mixing technologies, and/or tangential flow filtration is preferred. The position will support cross-functional teams across CMC, Research and Development, Pre-clinical and GMP Production, Quality, and Analytical Development. | 9/15/2023 |
| 4068 | Moderna Therapeutics Norwood, MA Engineer I, mRNA Process Development BS/MS degree in Bio/Chemical Engineering, Bio/Chemistry, Pharmaceutical Science, or related field Exp: 0-3 years |
Moderna is seeking an Engineer I to join the mRNA Process Development team to support development, scale up, transfer and commercialization of drug substances based on mRNA and lipid nanoparticle delivery technologies. Moderna is developing first-in-class mRNA-based vaccines and therapeutics. The mRNA is packaged into lipid nanoparticles for storage and delivery. The candidate will be focused on unit operations that are standard across the industry such as enzymatic reactions, normal and tangential flow filtration and chromatographic purification. The candidate will support commercial manufacturing processes and execute experiments to support deviation investigations and definition of appropriate process controls to increase process robustness. Applicants should enjoy working in a fast-paced, dynamic, and innovative environment. The successful candidate will possess strong skills in designing and executing high quality bioprocess experiments using quality by design (QbD) and Design of Experiment (DoE) methods, and will collaborate through cross-functional matrix teams. The person in this role will have the opportunity to develop on-line analytics, process modelling and process investigation support. Results will be presented to broader groups allowing great exposure to CMC Strategy, Regulatory, MS&T, and Quality. Prior experience of process development and process investigation accomplishments using scaled down models, QbD-principles and process characterization/modeling techniques are strong pluses. In this role, multi-day domestic and/or international travel (up to 20%) should be expected to support process investigations, support technology transfer and provide Person-in-Plant (PiP) support for commercial batches. The position will be based out of Moderna’s Norwood facility. | 9/15/2023 |
| 4069 | Moderna Therapeutics Norwood, MA Manufacturing Associate I, INT Drug Product, Nights STEM degree. Exp: 0-2 years’ |
A Manufacturing Associate I in the PCV Drug Product Operations group is responsible for vial filling, visual inspection, label and packaging (Fill Finish) of Moderna’s mRNA Drug Products. This position is located at Moderna’s GMP Manufacturing site in Norwood, MA. The shift in Fill Finish Drug Product Operations will be nights 12 hours 6:00PM-6:00AM on a 3 on/2 off/2 on/3 off/2 on/2 off schedule. The individual in this role will be part of a cohesive team responsible for supporting GMP mRNA-based medicines for evaluation in human clinical trials through execution of vial filling, visual inspection, and labeling and packaging activities. The successful candidate will be able to document all activities performed following cGMP guidelines and interact fluidly with peers and supervisors in Manufacturing, and cross-functionally with Manufacturing Sciences and Technology, Quality Control, Quality Assurance, Logistics and Process Development Technology Transfer counterparts. | 9/15/2023 |
| 4070 | Moderna Therapeutics Norwood, MA Research Associate, Analytical Technical Operations BS in Biochemistry, Molecular Biology, or a related field Exp: 1-3 years |
Moderna is seeking a molecular biologist to join Technical Development’s newly established Sequencing Center. In this laboratory-based position, the individual will routinely process sequencing samples, operate, and troubleshoot instruments including ABI 3730xl, Echo, Illumina MiSeq, NovaSeq, plate readers and liquid handlers. Experience with lab automation is a plus. The candidate must thrive in a fast pace high throughput environment, have a collaborative spirit, and be curious and willing to learn new techniques to push process development forward. | 9/15/2023 |
| 4071 | MP Biomedicals Solon, OH Production Chemist Bachelor of Science in Chemistry, Biochemistry, or Biology Exp: 0-3 years |
The production chemist will be trained on two different product lines. This position will rotate training through two manufacturing areas that include Immunology and Molecular Biology Liquids. Learn and be responsible for a wide variety of product formulation tasks. Follow and optimize production processes while following safety protocols. Produce quality research products in a timely fashion to meet customer demand. | 9/15/2023 |
| 4072 | DPT Laboratories St Albans, VT Chemist – 2nd Shift Bachelor's degree. Exp: 0-2 years |
Key responsibilities for this role include: Performs and documents the analysis of samples following approved test methods Calculate, check, and/or review data. Assist with method development, validation and transfer. Assist with instrument calibrations and maintenance. May work on analytical projects under direct supervision. Attend training classes and seminars as required. | 9/15/2023 |
| 4073 | DPT Laboratories Morgantown, WV Chemist I Bachelor's degree. Exp: 0-2 years |
Key responsibilities for this role include: Document laboratory activity in accordance with established procedures; including reagent preparation. Complete training as an Acquisition Controller on LC/MS systems. Demonstrate ability to understand and perform the major types of extraction methodologies employed within the lab Independently perform routine testing proficiently in accordance with all pertinent SOPs and lab practices Process and analyze data according to established procedures. Review data and associated documentation for compliance with Standard Operating Procedures. Operate analytical instrumentation including triple quadrupole HPLC-MS/MS systems and automated liquid handling workstations; including maintenance. Perform experiments in support of method development and validation with supervision. Prepare written responses to audit observations. The minimum qualifications for this role are: Must possess knowledge of Standard Operating Procedures, Guidelines, a basic understanding of chemistry, and OSHA regulations and procedures for the safe handling of chemicals. Must possess good communication and writing skills. Must possess the ability to multi-task and be accurate and precise. Must possess computer skills with working knowledge of Microsoft Office Suite, and instrumentation software. Position functions with supervision. Bachelor's degree (or equivalent) and 0-2 years of experience. However, a combination of experience and/or education will be taken into consideration. Ability to read and interpret complex business and/or technical documents. Ability to write comprehensive reports and detailed business correspondence. Ability to work with groups of people such as other departments and communicate known concepts. Ability to present to a group of departments. Proficiency in speaking, comprehending, reading and writing English are preferred. Ability to perform computations such as percentages, ratios, and rates. | 9/15/2023 |
| 4074 | Nanosyn Eagan, MN Microbiologist BS/BA in microbiology, biology or related field Exp: 1-2 years |
Element - Eagan is hiring a Microbiologist to work in a fast-paced environment directing laboratory-based studies evaluating antimicrobial products. The Microbiologist (a) performs and evaluates microbiological efficacy testing; (b) assists in data and report generation while maintaining a high level of scientific integrity; and (c) assists with and designs research and development (R&D) projects when implementing new methods or adapting current methods. | 9/15/2023 |
| 4075 | Nanosyn North Liberty, IA Microbiologist II Bachelor’s Degree in a laboratory science field from an accredited college or university. Certification by the American Society of Clinical Pathologis Exp: 1+ years |
Element has a current opening for a Microbiologist II at our North Liberty, IA location. Under general direction, the Microbiologist II performs moderate to highly complex laboratory testing and analysis on bacterial and fungal isolates to provide information to the SENTRY program, new drug development protocols and clinical trial protocols. Utilizes professional skill and judgement to perform a variety of microbiology procedures within the laboratory. | 9/15/2023 |
| 4076 | Natera San Carlos, CA Research Associate 2 B.S. degree in molecular biology, related field, or equivalent. Exp: 1-2 years |
The Research Associate 2 works under the guidance of a Sr Manager to execute verification and validation (V&V) studies, under design control, for next generation sequencing (NGS) assays. Works hands-on at the bench to carry out experiments, makes detailed observations, analyzes data and interprets results. | 9/15/2023 |
| 4077 | Natera San Carlos, CA Research Technician BS/BA in a biological science or equivalent required. Exp: 1-2 years |
The Research Technician performs routine laboratory research and development services. Works with a multidisciplinary team. Under nominal direction, performs a variety of basic and general laboratory research and sample management tasks determined by the field and scope of the research project. | 9/15/2023 |
| 4078 | Aliri Bioanalysis Salt Lake City , UT Analyst I Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1+ years |
Learns to analyze samples for various compounds and components in compliance with SOPs and regulatory agency guidelines. | 9/6/2023 |
| 4079 | Werfen Orangeburg, NY Scientist II Master's Degree Exp: 1 year |
Performs a broad range of laboratory work requiring application of professional judgment in the selection of specialized methods and techniques, and their application to specific tasks. | 9/18/2023 |
| 4080 | Inscripta Burlingame, CA Research Associate II/III, HTS BS/MS in Biology, Chemistry, Biochemistry or Chemical Engineering Exp: 1-2 years |
We are seeking a Research Associate II/III in our Burlingame location. The candidate will be a part of the high-throughput screening group, with primary responsibility for running screening operations for high-value products made by engineered strains of E. coli, S. cerevisiae, and other microbes. In addition, the candidate will contribute to the development and optimization of new high throughput and microfermentation assays, including automated sample preparation. They will work collaboratively with the rest of the team to optimize strain performance using our GenoScalerTM technology platform in rapid phenotyping of microorganisms. This hands-on position requires a desire and ability to work as a part of a multidisciplinary team, the ability to follow SOPs and run consistent operations, and an interest in continuously developing and improving our ability to characterize production strain through high throughput screening. | 9/6/2023 |
| 4081 | Integral Molecular Philadelphia, PA Research Associate I - (Job ID# 04182023) Bachelor’s degree in biology, bioengineering, or a related field? Exp: 1–2 years |
We are searching for a Research Associate I to join our dedicated group of scientists on the development and commercialization of biomedical technologies. We need someone who can effectively manage the challenges of performing high throughput assays, be self-reliant when executing tasks and contribute as a collaborative, supportive team member. A desirable candidate will have the skills to culture mammalian and/or bacterial cells, perform DNA mini-preps, and complete bacterial transformations and cell transfections. Familiarity with flow cytometry and liquid handling robots are a plus! | 9/6/2023 |
| 4082 | Ionis Pharmaceuticals Carlsbad, CA Research Associate, Cardiovascular Drug Discovery BS/MS in biology, molecular biology, biochemistry or related field. Exp: 1+ years |
The Cardiovascular, Renal & Metabolism (CVRM) Drug Discovery group seeks a Research Associate to join a multi-disciplinary team of energetic researchers who are working on validating new targets for cardiometabolic and renal diseases. The successful candidate will be responsible for the execution and analysis of studies utilizing rodent models of cardiometabolic disease as well as the evaluation of potential therapeutics for the treatment of heart failure. We are looking for a motivated individual with a strong attention to detail, capable of multi-tasking and who would succeed in a high paced atmosphere with minimal supervision. | 9/6/2023 |
| 4083 | Ionis Pharmaceuticals Carlsbad, CA Research Associate II/ Senior Research Associate, Core Antisense Research Master’s degree preferred in biochemistry, molecular biology or cell biology, or a B.S. Exp: MS: 0+ years; BS: >1-2 years |
We are seeking a highly qualified and motivated individual to perform basic research to increase our understand on how ASOs target RNA to modulate the expression of genes. The position offers the opportunity to do groundbreaking science and make discoveries that will create the next generation of ASO medicines. The selected candidate will become an integral part of an interdisciplinary and energetic team of scientists in the Ionis Core Research group. | 9/6/2023 |
| 4084 | Iovance Biotherapeutics Philadelphia, PA Aseptic Processing Tech - 2nd Shift [Contract to Hire] B.S. degree in biology, biochemistry, bioengineering, or related technical field. Exp: 0-2 years |
Iovance Biotherapeutics is seeking an Aseptic Processing Techician to join the team at 700 Spring Garden St, Philadelphia, PA.Co-located at the American Red Cross Penn Jersey Region, this Iovance facility produces a critical raw material used in the company’s TIL process. As an Aseptic Processing Technician, you will focus on the documentation for our processes. The ideal candidate will have a background in cell culture, aseptic gowning and qualification, and ISO class 5 cleanroom operations. This position works across different shifts. Depending on your assigned shift, you may be required to work overtime, weekends, and holidays to ensure the manufacturing process is completed. | 9/6/2023 |
| 4085 | Iovance Biotherapeutics Philadelphia, PA Aseptic Processing Technician [Contract to Hire] B.S. degree in biology, biochemistry, bioengineering, or related technical field. Exp: 0-2 years |
As an Aseptic Processing Technician, you will focus on the documentation for our processes. The ideal candidate will have a background in cell culture, aseptic gowning and qualification, and ISO class 5 cleanroom operations. This position works across different shifts. Depending on your assigned shift, you may be required to work overtime, weekends, and holidays to ensure the manufacturing process is completed. Iovance Biotherapeutics is seeking an Aseptic Processing Technician (contract-to-hire) to join the team at 700 Spring Garden St, Philadelphia, PA. Co-located at the American Red Cross Penn Jersey Region, this Iovance facility produces a critical raw material used in the company’s TIL process. The critical raw material is processed from leukapheresis units and frozen. Processing is performed in an ISO 7 cleanroom within an ISO 5 biological safety cabinet. | 9/6/2023 |
| 4086 | Iovance Biotherapeutics Philadelphia, PA Quality Control Analyst, Environmental Monitoring - 2nd Shift [Contract to Hire] Bachelor’s degree in a relevant discipline (biological sciences or equivalent). Exp: one (1) year |
Iovance Biotherapeutics is seeking a Quality Control Analyst to join the team at 700 Spring Garden St, Philadelphia, PA.Co-located at the American Red Cross Penn Jersey Region, this Iovance facility produces a critical raw material used in the company’s TIL process. The critical raw material is processed from leukapheresis units and frozen. The QC Analyst will support quality control environmental monitoring operations at Iovance’s. The quality control environmental monitoring programs include in-process and final drug product microbial testing such as bioburden, endotoxin, gram stain, environmental monitoring, compressed gas monitoring, and/or sterility techniques. | 9/6/2023 |
| 4087 | Cambridge Isotope Laboratories Xenia, OH Quality Assurance Associate Bachelor’s Degree in chemistry or related science preferred. Exp: 0-2 years |
Cambridge Isotope Separations (CIS) is searching for a GMP Quality Assurance (QA) Associate located in Xenia, Ohio. Cambridge Isotope Laboratories (CIL) and CIS are the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. Under general supervision, the primary responsibility of the QA Associate is to work as a team member to ensure and maintain the Company’s cGMP (Current Good Manufacturing Practices) compliance.Cambridge Isotope Separations (CIS) is searching for a GMP Quality Assurance (QA) Associate located in Xenia, Ohio. | 9/7/2023 |
| 4088 | Cambridge Isotope Laboratories Tewksbury, MA Quality Control Analyst I BS or MS degree in Chemistry or other relevant science degree. Exp: One or more years |
Cambridge Isotope Laboratories, Inc. has an outstanding opportunity to join our GMP Quality Control team as a Quality Control Analyst I based onsite in our Tewksbury, MA headquarters. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. The Quality Control Analyst I is responsible for conducting routine analysis of GMP/ISO materials including: Raw materials, in-process and finished products under general supervision and in accordance with standard operating procedures (SOPs). The analyst will compile data for documentation of test procedures and prepare reports. They also calibrate and maintain lab equipment and participate in general upkeep of the laboratory.Cambridge Isotope Laboratories, Inc. has an outstanding opportunity to join our GMP Quality Control team as a Quality Control Analyst I based onsite in our Tewksbury, MA headquarters. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. The Quality Control Analyst I is responsible for conducting routine analysis of GMP/ISO materials including: Raw materials, in-process and finished products under general supervision and in accordance with standard operating procedures (SOPs). The analyst will compile data for documentation of test procedures and prepare reports. They also calibrate and maintain lab equipment and participate in general upkeep of the laboratory. | 9/7/2023 |
| 4089 | Cambridge Isotope Laboratories Andover, MA Chemist MS in Chemistry Exp: 1-3 years |
Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Chemist based onsite in our Andover, MA location. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. Under the supervision of a group leader or supervisor, the Chemist will work alongside an experienced scientist executing syntheses of isotopically labeled (13C, 15N, 18O and D isotopes) targets utilizing highly detailed SOPs and procedures. | 9/7/2023 |
| 4090 | Fresenius Kabi Melrose Park & Chicago, IL Associate Scientist (Nights) BS/BA degree in Science or related field. Exp: 0+ years |
The Associate Scientist will be responsible for collection and testing of routine environmental monitoring samples within aseptic processing fill lines, Isolator fill line, compounding, sterility suite, and component preparation areas for aseptic lines (Building A) and clean rooms areas in new expansion Building B. Collect and test utility samples such as WFI, clean steam and compressed gases. Monitors environmental conditions in laboratory areas during test sessions. Reports testing results and documents in compliance with cGMP and GLP standards. Provides support to Scientist, Lead Scientist, and Supervisor. Prepares media, reagents, sanitizing solutions and equipment for use in testing. | 9/7/2023 |
| 4091 | Fresenius Kabi Melrose Park & Chicago, IL Scientist I B.S. degree in Chemistry or Biology, or equivalent physical science. Exp: 1 year |
Responsible for an intermediate level of expertise in analytical chemistry, chromatographic methods of analysis and instrumentation, including troubleshooting. Independently executes protocols, verifications, method transfers in support of senior level personnel. Directs and provides guidance to associate scientists. | 9/7/2023 |
| 4092 | Fresenius Kabi Melrose Park & Chicago, IL Associate Scientist (Nights) BS/BA degree in Science or related field. Exp: 0+ years |
The Associate Scientist will be responsible for collection and testing of routine environmental monitoring samples within aseptic processing fill lines, Isolator fill line, compounding, sterility suite, and component preparation areas for aseptic lines (Building A) and clean rooms areas in new expansion Building B. Collect and test utility samples such as WFI, clean steam and compressed gases. Monitors environmental conditions in laboratory areas during test sessions. Reports testing results and documents in compliance with cGMP and GLP standards. Provides support to Scientist, Lead Scientist, and Supervisor. Prepares media, reagents, sanitizing solutions and equipment for use in testing. | 9/7/2023 |
| 4093 | Fresenius Kabi Melrose Park & Chicago, IL Associate Scientist B.S. in Chemistry, Biology or related physical science. Exp: 1+ years |
The Associate Scientist is responsible for performing entry level chemical testing to support raw material, in-process, stability, and finished products as required for Quality Control. Effectively communicates work and results both orally and in writing. | 9/7/2023 |
| 4094 | Fresenius Kabi Grand Island , NY SCIENTIST (Chemistry) - 3rd Shift B.S. in Chemistry, Biology, or related physical science. Exp: 1-4 years |
A Scientist I in Quality Control is responsible for an intermediate level of expertise in analytical chemistry, chromatographic methods of analysis and instrumentation, including troubleshooting. Directs and provides guidance to associate scientists. | 9/7/2023 |
| 4095 | Fresenius Kabi Grand Island , NY ASSOCIATE SCIENTIST - 2nd Shift Chemistry B.S. in Chemistry, Biology, or related physical science. Exp: 0-2 years |
An Associate Scientist is responsible for performing entry level chemical testing to support raw material, in-process, stability, and finished products as required for Quality Control. Effectively communicates work and results both orally and in writing. | 9/7/2023 |
| 4096 | Fresenius Kabi Grand Island , NY ASSOCIATE SCIENTIST - 1st Shift Chemistry B.S. in Chemistry, Biology, or related physical science. Exp: 0-2 years |
An Associate Scientist is responsible for performing entry level chemical testing to support raw material, in-process, stability, and finished products as required for Quality Control. Effectively communicates work and results both orally and in writing. | 9/7/2023 |
| 4097 | Janssen Pharmaceuticals Brisbane, CA Associate Scientist, Oligonucleotide Biology - RNA, Gene Therapy and Delivery M.S. Exp: 1 year |
We are seeking an accomplished and curious Associate Scientist to join our Oligonucleotide Biology team in the discovery of targeted oligonucleotide therapeutics. At our San Francisco Bay Campus in Brisbane, the Associate Scientist will help develop and implement diverse in vivo and in vitro assays, while collaborating with highly motivated teams to optimize siRNA/mRNA therapeutics. A strong candidate will have expertise in in vivo and ex vivo techniques, cell-based assays, and excellent interpersonal talents. | 9/19/2023 |
| 4098 | Janssen Pharmaceuticals Spring House, PA PK Analyst - Associate Scientist I/II M.S. Exp: 1-3 years |
Janssen Research & Development, L.L.C., a division of Johnson & Johnson's Family of Companies is recruiting for a PK Analyst to join the team as an Associate Scientist I/II located in Spring House, PA. This is a scientific position within the nonclinical pharmacokinetic (PK) assay development and bioanalysis team within the Development PK group of the Bioanalytical Discovery and Development Sciences (BDDS) of Janssen R&D. Our team develops, validates, and conducts bioanalytical studies related to large molecule biotherapeutic drugs in a highly regulated environment (GLP and GCP regulations). We work across all therapeutic areas within Johnson & Johnson, spanning nonclinical studies to post-market clinical development | 9/19/2023 |
| 4099 | Janssen Pharmaceuticals Danvers, MA Product Development Engineer I, Surgery BS in Mechanical Engineering or directly related scientific discipline, MS Preferred. Exp: 1-3 years |
Abiomed, part of Johnson & Johnson MedTech, is recruiting for a Product Development Engineer located in Danvers, MA. The ideal Product Development candidate will be goal, data-driven, detail oriented; and experienced in the medical industry. The Product Development Engineer will lead complex technical tasks and engineering process improvements, collaborate with senior and junior staff, develop new products, and provide engineering support for existing products. | 9/19/2023 |
| 4100 | J-Star Cranbury, NJ Research Scientist Master’s degree in Chemistry, Chemical Engineering, or Materials Science and Engineering. Exp: one year |
Research Scientist wanted for J-Star Research Inc in Cranbury, New Jersey. Must have knowledge of FDA regulations, Polymorph characterization, crystallization, distillation, quantitative analysis, Thermo-Property test, HPLC, UPLC, IC, LC-MS, Methodology Development, and column chromatography. Job duties to be performed: Perform Active Pharmaceutical Ingredient (API) crystallization process in compliance with cGMP and FDA regulations, utilizing polymorph and physical properties analytical tools, including spectroscopy, microstructure monitoring, separation, and solvent selection. Conduct crystallization process development by conducting studies involving materials engineering and experimental design; Generate materials for pharmaceutical research. Participate in the scale-up development of enabling technology and experiments to facilitate the co-processing and development of API. Conduct routine stability, performance, and evaluation studies for solid state characterization and pre-formulation support using Polymorph characterization. Conduct early drug crystallization process development for high potency compounds and controlled substances. Purify pharmaceutical compounds using column chromatography, crystallization, trituration, extraction, and distillation. | 9/8/2023 |
| 4101 | J-Star Cranbury, NJ Senior Research Chemist Master’s degree in Chemistry. Exp: one year |
Senior Research Chemist wanted for J-Star Research Inc in Cranbury, New Jersey. Must have knowledge of synthetic organic chemistry, methodology development, reaction optimization, quantitative assays, HPLC, LC/MS, NMR, IR, purification techniques including column chromatography, crystallization, and distillation. Job duties to be performed: Plan and execute process chemistry R&D proposals for pharmaceutical and biotechnology projects in compliance with FDA regulations. Design synthetic routes for the preparation of small molecule pharmaceuticals with principles of synthetic organic chemistry. Develop and optimize chemical methodologies and processes to synthesize active pharmaceutical ingredients (API) and chemical intermediates utilizing reaction route scouting, and design of experiments (DoE). Scale up the manufacturing process in non-GMP and cGMP kilolabs with operation of the corresponding process equipment. Collaborate in a cross functional team with QA, QC and engineers to support the cGMP production. Purify pharmaceutical compounds using column chromatography, crystallization, and distillation.Senior Research Chemist wanted for J-Star Research Inc in Cranbury, New Jersey. Must have knowledge of synthetic organic chemistry, methodology development, reaction optimization, quantitative assays, HPLC, LC/MS, NMR, IR, purification techniques including column chromatography, crystallization, and distillation. Job duties to be performed: | 9/8/2023 |
| 4102 | Jubilant HollisterStier Spokane, WA Scientist I-II-III, QC Bachelor’s Degree in Chemistry, Biology, or related hard science required. Exp: Scientist I: 0 years; Scientist II: + 1 year |
The QC Scientist I/II/III performs the analysis on allergenic and client components, raw materials, intermediates, and finished products following written procedures, providing the data required to determine raw material/product disposition. Essential responsibilities include: Analyze raw materials, in-process, stability and final container products according to established procedures, and as directed by the supervisor. Record and review data in accordance with GxP to meet regulatory requirements and provide information relevant to product disposition. Perform studies to assess product or procedural problems under the direction of the supervisor. Assist in other forms of troubleshooting/investigations as directed. Prepare reports and assist with document revisions as directed by the Supervisor. | 9/19/2023 |
| 4103 | KBI Biopharma Durham - Hamlin Rd, NC Research Associate I/II BS degree in chemistry, biochemistry, or related area OR MS degree in chemistry, biochemistry or related area. Exp: BS: 0-2+ years'; MS: 0+ years’ |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. | 9/8/2023 |
| 4104 | KBI Biopharma Durham - National Way, NC Manufacturing Associate I/II-Upstream (Nights) Manufacturing Associate I: Bachelor’s degree in a related scientific or engineering discipline. Exp: MAI: 0-2 years’ |
This position is on a 2-2-3 schedule, with the hours 7p-7a. The Manufacturing Associate I/II – Upstream is responsible for the execution of production activities for early and late-phase Cell Culture programs within a GMP environment. The Manufacturing Associate I/II – Upstream must follow the instructions depicted in SR’s, EPR’s, BR’s, SOP’s and forms. Additionally, must ensure all work is conducted following Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and Good Laboratory Practices (GLP); including ‘Right the First Time’ (RFT). Upstream is responsible for the execution of production activities for early and late-phase Cell Culture programs within a GMP environment. The candidate will maintain a sense of ownership of the production processes, manufacturing environment and facility. They will be exposed to cell culture media preparation, shake flask operations, seed expansion, bioreactor setup and operations, cell culture harvest setup and operations, and aseptic technique; as well as to cell culture analytical tools and general biotechnology auxiliary equipment (pumps, sterile tubing welders and sealers, pH/Conductivity/osmolarity meters). Following task execution, the Manufacturing Associate I/II will review the executed production records (SR’s, ERP, and BR’s) to ensure GxP compliance. This position is on a 2-2-3 schedule, with the hours 7p-7a. The Manufacturing Associate I/II – Upstream is responsible for the execution of production activities for early and late-phase Cell Culture programs within a GMP environment. | 9/8/2023 |
| 4105 | KBI Biopharma Boulder, CO Manufacturing Associate I/II (Nights) Bachelor’s degree. Exp: 0-5 years |
This position will be on a 4-3 night shift schedule. The hours are 7:00 pm to 7:00 am. Coordinate and perform cGMP manufacturing operations for manufacturing biopharmaceutical products. Ensure the effective use of material, equipment, and personnel while making products at high-quality levels | 9/8/2023 |
| 4106 | KBI Biopharma Durham - Hamlin Rd, NC Manufacturing Associate I/II-Upstream\ Manufacturing Associate I: Bachelor’s degree in a related scientific or engineering discipline. Exp: 0-2 years’ |
This position is on a 2-2-3 shift, 7a-7p. The Manufacturing Associate I/II – Upstream is responsible for the execution of production activities for early and late-phase Cell Culture programs within a GMP environment. The Manufacturing Associate I/II – Upstream must follow the instructions depicted in SR’s, EPR’s, BR’s, SOP’s and forms. Additionally, must ensure all work is conducted following Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and Good Laboratory Practices (GLP); including ‘Right the First Time’ (RFT). Upstream is responsible for the execution of production activities for early and late-phase Cell Culture programs within a GMP environment. | 9/8/2023 |
| 4107 | KBI Biopharma Boulder, CO Manufacturing Associate I/II Bachelor’s degree. Exp: 0-5 years |
This position will be on a 4-3 day shift schedule. The hours are 7 am to 7 pm. Coordinate and perform cGMP manufacturing operations for manufacturing biopharmaceutical products. Ensure the effective use of material, equipment, and personnel while making products at high-quality levels | 9/8/2023 |
| 4108 | KBI Biopharma Durham - Hamlin Rd, NC Research Associate II MS degree in chemistry, biochemistry or related area. Exp: 0+ years’ |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. | 9/8/2023 |
| 4109 | KBI Biopharma Durham - Hamlin Rd, NC Manufacturing Associate I/II Upstream (Nights) Manufacturing Associate I- Bachelor’s degree in a related scientific or engineering discipline. Exp: 0-2 years’ |
This position operates on a 2-2-3 schedule with the hours of 7:00 pm - 7:30 am. The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Manufacturing Associate must follow written, approved procedures and forms to ensure all work is conducted “Right First Time” (RFT) following Good Manufacturing Practice (GMP), including good documentation practices, and/or Good Laboratory Practice (GLP). As needed, the Manufacturing Associate will work individually or on teams to author standard operating procedures (SOPs) or Master Batch Records (MBRs); write corrective and preventive actions (CAPAs); and specify, commission, and qualify new equipment. The Manufacturing Associate will be responsible for upstream unit operations (seed expansion, bioreactor operations, cell culture harvest). The Manufacturing Associate will have a working knowledge of upstream processing equipment (incubators, biosafety cabinets, bioreactors, cell counters, blood gas analyzers, metabolite testing equipment). Additionally, the manufacturing associate will have knowledge of general bioprocessing equipment such as filters, filter integrity testers, balances, pumps, pH/conductivity meters, and disposable technologies (disposable bags, sterile tubing welders, tubing sealers). Following task execution, the Manufacturing Associate will review the executed production records and logbooks to ensure GxP compliance. | 9/8/2023 |
| 4110 | Khloris Biosciences San Jose, CA Cell Therapy Manufacturing Technician B.S. degree in biology, biochemistry, bioengineering, or related technical field. Exp: 0-5 years |
Khloris Biosciences, Inc. is seeking innovative and highly motivated cell therapy manufacturing technician to join our team. The selected candidate will work closely with lead manufacturing technicians, scientists, participate in project and team meeting, and work in a multidisciplinary environment. The duties of this position will involve supporting a multidisciplinary manufacturing team in developing Khloris cell therapy platforms. The ideal candidate will have hands-on expertise and comprehensive understanding of cell therapy manufacturing processes. | 9/8/2023 |
| 4111 | Khloris Biosciences San Jose, CA Research Associate Positions - Cancer Vaccine B.S. required in appropriate discipline required (e.g., immunology, cell biology, molecular biology). Exp: 1+ years |
Khloris Biosciences, Inc. is seeking innovative and highly motivated research associates to join the cancer vaccine team. The successful candidate(s) will be responsible for supporting cancer vaccine projects on a preclinical level. Prior experience with rodent tumor models and/or in vitro immune assays is preferred. The selected candidate will work closely with other scientists, participate in project teams, and work in a multidisciplinary environment in order to advance projects. | 9/8/2023 |
| 4112 | Lannett Seymour, IN Raw Materials Chemist I BS Degree in Chemistry or related field. Exp: 0+ years |
This position is primarily responsible for the laboratory testing of raw materials and packaging materials or in-process, release and stability samples for commercial drug products. | 9/8/2023 |
| 4113 | Lannett Seymour, IN Raw Materials Chemist I BS Degree in Chemistry or related field. Exp: 0+ years |
This position is primarily responsible for the laboratory testing of raw materials and packaging materials or in-process, release and stability samples for commercial drug products. | 9/8/2023 |
| 4114 | Lannett Seymour, IN Product Chemist I BS Degree in Chemistry or related field. Exp: 0+ years |
This position is primarily responsible for the laboratory testing of in-process, release and stability samples for commercial drug products. | 9/8/2023 |
| 4115 | Lantheus Medical Imaging Billerica, MA Process Engineer 1 Bachelor’s Degree in Engineering or related science oriented discipline. Exp: 1 to 2 years |
An ideal candidate would have strong background in assessing and processing quality events inclusive of deviations, CAPA plans and actions, and investigations. Be able to use project management skills to organize and lead cross functional teams through data-based decision making for root cause investigations, technical transfers, or project improvements. Support larger projects collaborating across multiple teams. Strong partnership skills to build and maintain relationships. | 9/8/2023 |
| 4116 | Legend Biotech Raritan, NJ QC Analyst Bachelor’s Degree in Science, Engineering or equivalent technical discipline is required. Exp: 1 years |
The QC Analyst, CAR-T Manufacturing is an exempt level position with responsibilities for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment. | 9/19/2023 |
| 4117 | Legend Biotech Raritan, NJ QC Analyst (3rd shift) Bachelor’s Degree in Science, Engineering or equivalent technical discipline is required. Exp: 1 years |
The QC Analyst, CAR-T Manufacturing is an exempt level position with responsibilities for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment. | 9/19/2023 |
| 4118 | Galatea Surgical Sumter, SC Quality Engineer II (Onsite) MSc. Degree Exp: 1 years |
BD is seeking a Quality Engineer II to join the team at our medical device manufacturing site in Sumter, SC. As a Quality Engineer II, you'll play an integral role in maintaining compliance with ISO and FDA guidelines while collaborating with local, US-based and international resources. You'll be responsible for building and implementing strategic quality plans and regulatory compliant operating procedures that support routine validation, as well as expansion and upgrade projects. If you're passionate about quality and are looking for a challenging and rewarding career, we want to hear from you! | 8/29/2023 |
| 4119 | Global Blood Therapeutics Kalamazoo, MI QC Laboratory Analyst II (2nd Shift) Bachelor´s degree in Chemistry, Biochemistry or related science degree Exp: 0-1 years |
This position is for a testing analyst in the Kalamazoo QO DP Laboratory working on second shift (3:00PM-11:30PM). Opportunity for schedule flexibility exists as the Laboratory supports business and customer needs on weekends and holidays. Technologies employed in the Rapid Turn Laboratory include HPLC, GC, IC, Titrations, Karl Fisher, UV, FTIR, SG, RI, LOD, and general analytical procedures. | 8/29/2023 |
| 4120 | Global Blood Therapeutics Cambridge, MA Senior Associate Scientist- BMD Biotherapeutic Expression and Purification MS in Chemistry, Biochemistry, Biology, Biomedical Sciences, or a related discipline Exp: 0-2 years |
Pfizer's BioMedicine Design (BMD) is seeking a highly motivated Biochemist/Molecular Biologist to join the Biotherapeutic Expression and Purification group (BEP) in Cambridge, MA. The qualified candidate will play an essential role in a dynamic DNA production and protein expression research laboratory. This group provides non-GMP transient protein lead production support across Pfizer's diverse biotherapeutic discovery portfolio, meeting the in-vitro and in-vivo needs of Pfizer’s research units and their pre-clinical therapeutic programs. The BEP group is looking for a successful candidate who can provide DNA production support for protein expression and purification activities. The ideal candidate is expected to have a strong background in molecular biology techniques, as well as experience in nucleic acid production and analysis. The selected individual will cultivate bacterial cultures and perform large-scale DNA production activities, following standardized protocols. They will be a key contributor to the scientific team responsible for protein expression and purification. | 8/29/2023 |
| 4121 | Global Blood Therapeutics Andover, MA Production Engineer I Bachelor's degree Exp: 1-2 years |
Provide engineering and technical support related to the installation, startup/commissioning, testing, and qualification, sustained operation and maintenance of process and automated equipment and systems within a biopharmaceutical clinical manufacturing facility, as well as commercial/ clinical changeover and tech transfer activities. This may include startup of production equipment such as bioreactors, ultrafiltration skids, Clean – In – Place (CIP) skids, and other support equipment. | 8/29/2023 |
| 4122 | Global Blood Therapeutics Andover, MA Quality Engineer II Bachelor's degree Exp: 0+ years |
You will have knowledge of process equipment and systems and manufacturing operations with the primary responsibility to execute process and equipment operation activities during manufacturing operations. Due to your expertise in the manufacturing domain, you may participate in training for operational qualifications and assist the Team Lead or other team members as needed. You will conduct all activities in accordance with Company policies and standard operating procedures, Pfizer Values, and global regulatory guidelines, environmental guidelines etc. As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative team environment for your colleagues. It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe. | 8/29/2023 |
| 4123 | Global Blood Therapeutics Andover, MA QC Scientist II Bachelor's degree Exp: 0+ years |
You will be a member of Pfizer’s dedicated and highly effective Quality Control Microbiology team. You will be responsible for analyzing microbiological products to support our quality programs. Your contribution to the QC Micro team will help Pfizer provide safe drugs to patients. As a QC Scientist II, your experience in applying knowledge of principles, concepts, and practices of the discipline will make you a critical member of the team. Your skill and knowledge will help in making decisions that require choosing among limited options. Your being proactive in team discussions will help in creating an environment of collaboration. It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe. | 8/30/2023 |
| 4124 | Global Blood Therapeutics Andover, MA Tech Transfer Engineer I Bachelor's degree Exp: 0+ years |
Provide engineering support related to the evaluation, technology transfer, startup, and qualification of new and existing equipment, facilities, and utilities in support of existing product campaigns and new product introduction. Engineering support will include basic equipment and automation troubleshooting and project execution. This may include production equipment such as bioreactors, ultrafiltration skids, Clean – In – Place (CIP) skids, chromatography skids, and other support equipment. | 8/30/2023 |
| 4125 | Global Blood Therapeutics Andover, MA QA Specialist III Masters Exp: 1+ years |
As a QA Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate in explaining difficult issues and establishing consensus between teams. It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe. | 8/30/2023 |
| 4126 | Genentech Hillsboro, OR Manufacturing Engineer (Cell & Gene Therapy) Bachelor’s degree in cellular or molecular biology or engineering preferred. Exp: 1 year |
Genentech is offering an exciting opportunity for the right individual to join Genentech’s Hillsboro Individualized Therapies (HIT) team, working to bring new medical advancements from development stages to commercial manufacturing. This is an exciting opportunity to work closely with emerging technology including but not limited to individualized DNA/RNA therapies, Cell therapies, and Stem Cell therapies. This is the start-up headquarters for Genentech’s individualized and cell therapies division where we will establish the industry standard. As a member of the team you would be responsible for supporting multi-phase technology transfers and production. | 8/31/2023 |
| 4127 | Genentech Hillsboro, OR Manufacturing Asset Engineer I, HTO (Two Year Term) B.S or higher in Mechanical Engineering, Electrical, Chemical, Biochemical, or related discipline. Exp: 1-2 years’ |
The Asset Engineer is responsible for supporting the design, operation, control and optimization of manufacturing equipment at HTO. The position serves as the equipment owner and is engaged in development, qualification, data analysis, troubleshooting, and continuous improvement activities. The Asset Engineer plays a key role in day-to-day operations, as well as design and delivery of local and major capital projects, and interacts with a cross-functional team to deliver on business objectives. | 8/31/2023 |
| 4128 | Genentech Oceanside, CA Manufacturing Technical Specialist II/ Engineer I Bachelor's or Master's degree in Engineering or Life Sciences. Exp: 0-4 years |
Responsible for supporting operations in the Oceanside Pilot Plant and Process Engineering Purification/Analytical Lab. Deliverables include but are not limited to: HPLC-based analytics, rapid bioburden/endotoxin, lab scale and pilot scale chromatography, UFDF operations, buffer prep, column packing, equipment maintenance and preparation of technical reports. May commission new equipment, troubleshoot equipment and systems, develop new equipment requirements and operating parameters, and provide factory and site acceptance testing. Provide scientific and technical support to GMP Manufacturing Operations in a multi-product, large scale, automated biopharmaceutical facility. Support process validation through large and small-scale studies, protocol and report preparation, validation sampling, and sample shipments. | 8/31/2023 |
| 4129 | Genentech South San Francisco, CA Technical Development Scientist - Protein Analytical Chemistry BS or MS in biological or chemical sciences, or related disciplines. Exp: 0 to 2+ years |
We are seeking a highly motivated individual to join the department of Protein Analytical Chemistry (PAC) (within PTDU) as a Technical Development Scientist. A successful candidate will be expected to work hands-on in the laboratory to generate analytical data in support of the pipeline and technical development projects. This will include analytical characterization and testing as well as development and execution of analytical methods. The candidate may also collaborate with cross functional colleagues and contribute to manufacturing process development and clinical trial and commercialization-enabling regulatory filings (e.g. BLAs and INDs). This candidate is expected to be a good lab citizen, following all environmental health and safety guidelines and maintaining lab space and instruments in good working order. The individual will maintain excellent documentation of all work, including electronic laboratory notebooks, and will author technical reports. Additionally, the individual will be responsible for presenting experimental results to technical development teams, the PAC department, and other stakeholders on a regular basis. Candidates applying should be passionate about science, exceptionally productive, data-driven and should enjoy the challenges associated with complex problem-solving. Candidates must be highly self-motivated and willing to work independently or as a part of multi-disciplinary teams to ensure the delivery of Genentech’s protein pharmaceutical pipeline. | 8/31/2023 |
| 4130 | Genentech Oceanside, CA Bioprocess Manufacturing Technician (Contract) Preferred - Degree in Life Sciences/Engineering, Associate’s or Biotech certificate from approved program. Exp: 0+ years |
As a Bioprocess Manufacturing Technician, you will be responsible for producing medicine in a highly automated and controlled environment. Each product has a specific recipe; you will follow this recipe, along with the standard operating procedures, to operate the production equipment across various areas, including raw material dispensing/aliquoting, cell culture and purification. You will maintain records and follow all the steps necessary to comply with regulatory requirements within a current Good Manufacturing Practices (cGMP) environment. This is a contract role with the possibility of conversion to a permanent employee position | 8/31/2023 |
| 4131 | Genentech South San Francisco, CA Validation Engineer (Contractor) B.S. degree in Science or Engineering. Exp: 1-2 years |
Genentech's Device Development team is searching for a Validation Engineer to assist, lead, and execute validation activities (e.g., equipment qualification, computer system validation) and manage discrepancies and changes to Qualified/Validated systems. The candidate should have knowledge in Laboratory equipment qualification & validation process, data integrity (CFR Part 11 Compliance) implementation, cGMP documentation, Change Management, and operational maintenance of Laboratory equipment.Genentech's Device Development team is searching for a Validation Engineer to assist, lead, and execute validation activities (e.g., equipment qualification, computer system validation) and manage discrepancies and changes to Qualified/Validated systems. | 8/31/2023 |
| 4132 | GenWay Biotech San Diego, CA Research Associate I/II – Molecular Biology B.S. or M.S. in life science or related subject. Exp: 1+ year |
Aviva Systems Biology is a fast paced, mid stage life sciences research tools company located in San Diego, CA. We commercialize life science tools and reagents for research, drug discovery, and diagnostics. | 9/1/2023 |
| 4133 | GenWay Biotech San Diego, CA Manufacturing Associate I/II B.S. or M.S. in life science or related subject. Exp: 1+ year |
The Manufacturing Associate will assist in the production of recombinant proteins and other biological products under GMP guidelines. Manufacturing team members to develop products in support of the company’s growth strategy. This is a highly collaborative role where you will directly impact the company’s revenue growth. The Manufacturing Associate works as part of a multidisciplinary team performing standard molecular biology techniques, protein purification and analysis, and cell culture maintenance. Clear communication skills, careful execution with attention to details, and excellent record keeping are a must. The ideal candidate will thrive in a fast-paced, dynamic environment as a part of a highly focused team of motivated scientists. | 9/1/2023 |
| 4134 | GigaGen San Carlos, CA Senior Research Associate, Analytical/Assays Master’s degree in Chemistry, Life Sciences, or related discipline. Exp: 1 year |
GigaGen, a subsidiary of Grifols, seeks a talented, highly motivated Senior Research Associate to support the analytical and functional analysis of our diverse antibody therapeutics pipeline, including the development and implementation of analytical and functional assays for characterizing antibodies and antibody derivatives. This position will offer exposure to drug development, from early research through development/manufacturing, with ample opportunity to learn new methods, design experiments, and present your work. | 9/1/2023 |
| 4135 | GigaGen San Carlos, CA Research Associate Bachelor’s degree in Life Sciences or related discipline. Exp: 1 year |
GigaGen, a subsidiary of Grifols, seeks a talented, highly motivated Research Associate to support our diverse antibody therapeutics pipeline. This position will offer exposure to drug development, from early research through development/manufacturing, with ample opportunity to learn new methods, design experiments, and present your work. | 9/1/2023 |
| 4136 | Glaukos San Clemente, CA Microbiologist Bachelor's Degree in Microbiology, Biology, or Biochemistry. Exp: 1-2 years |
The Microbiologist/QA Engineer-Pharma and Medical Devices - position will be based in San Clemente, CA and will directly support the manufacture of innovative ocular medical devices and pharmaceuticals. This role includes ensuring proper execution of Environmental Monitoring tasks, reviewing routine and event-based environmental related project protocols, validations, reports, and data assessment. The candidate will assist with EM testing, bioburden testing, growth promotion and other microbiological testing within the lab. The candidate will coordinate and monitor EM related activities to ensure quality and on time completion of EM related tasks. The candidate is also expected to work collaboratively with internal cross-functional groups - R&D, Operations, Facilities - and with external contract vendors. | 9/1/2023 |
| 4137 | Glaukos San Clemente, CA Engineer I/II (Pharma Operations) Bachelor’s degree in Engineering or Science. Exp: 6 months - 2 years |
Responsible for manufacturing of development, pilot, clinical, verification/validation, stability study campaigns, and commercial production whether internal or at CMO (hands-on as needed). | 9/1/2023 |
| 4138 | Grand River Aseptic Manufacturing Grand Rapids , MI Aseptic Manufacturing Associate (Weekend Shift) Bachelor’s degree Exp: 0-1 year |
The Aseptic Manufacturing Associate (AMA) is responsible for performing various routine manufacturing tasks following established procedures and cGMP regulations under guidance of a production supervisor and/or management. Weekend shift hours are Friday, Saturday, Sunday, 12-hour shifts (either 6am-6pm, or 6pm-6am). Weekend shift differentials and paid breaks! | 9/1/2023 |
| 4139 | Grand River Aseptic Manufacturing Grand Rapids , MI Aseptic Manufacturing Associate (2nd and 3rd shifts) Bachelor’s degree Exp: 0-1 year |
The Aseptic Manufacturing Associate (AMA) is responsible for performing various routine manufacturing tasks following established procedures and cGMP regulations under guidance of a production supervisor and/or senior management. | 9/1/2023 |
| 4140 | Grand River Aseptic Manufacturing Grand Rapids , MI QC Chemist (3rd Shift) Bachelor’s degree in Chemistry and/or other related discipline (e.g. Biochemistry, Biotechnology). Exp: 1-3 years |
The Quality Control Chemist is responsible for supporting quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties will include, but are not limited to, providing general laboratory support for raw material, in-process, stability, and finished product testing. | 9/1/2023 |
| 4141 | Grifols Clayton, NC Assistant/Associate Biologist BS/BA degree in a life science field, medical technology, or related curriculum is required. Exp: 6 mos+ years |
The incumbent is responsible for performing complex laboratory analysis of plasma and plasma products in a GMP laboratory. Responsibilities include sample accessioning, sample preparation, reagent preparation, testing, result calculation, as well as quality control of assays and equipment. The incumbent will also support assay validation, method transfer, reagent and control qualification, and laboratory maintenance activities as assigned. Must be comfortable working with infectious material on a daily basis. Person must be able to work in a biological safety cabinet and comfortable working with a microscope for several hours at a time. Candidates for the position must be proficient with using micropipettes and serological pipettes while making dilutions and serial dilutions. Must be able to perform tasks by following SOP’s and oral instructions. Must have precise, legible, and organized documentation skills. Candidates must also be willing to perform their share of cleaning duties and housekeeping. This position is responsible for performing bioburden and endotoxin testing of in-process product samples and raw materials to support plasma production processes, including process and equipment activities. The Quality Control Sterility & Microbiology department must maintain adequate staffing to support all production operations 24 hours per day, 7 days a week. In addition to in-process product monitoring, this position may also assist with environmental monitoring of production and testing areas. This position is part of the budgeted staff necessary to complete this sampling and testing and to ensure that Clayton site production processes and production areas remain in a state of control. | 9/1/2023 |
| 4142 | Grifols Clayton, NC Assistant/Associate Biologist BS degree in biology, chemistry, or related field. Exp: 6-12 months |
This position is responsible for performing environmental monitoring of fill lines in B300 and SFF and also environmental monitoring of all classified production areas, including sampling of site utility systems. Environmental Assurance department must maintain adequate staffing to support all filling operations 24 hours per day, 7 days a week. In addition to routine environmental monitoring of the aseptic fill lines, this position is also responsible for executing the Quality Oversight program for the fill lines and also provides quality control approval of air flow visualizations conducted on site. This position is part of the budgeted staff necessary to complete this sampling and testing and to ensure that Clayton site environmental monitoring of the aseptic fill lines and other production areas and utility systems remain in a state of control. Must be able to perform tasks by following SOP’s and oral instructions. Must have precise, legible, and organized documentation skills. Candidates must also be willing to perform ones share of cleaning duties and housekeeping. In addition to routine environmental monitoring of the aseptic fill lines, this position is also responsible for executing the Quality Oversight program for the fill lines and also provides quality control approval of air flow visualizations conducted on site. This position is part of the budgeted staff necessary to complete this sampling and testing and to ensure that Clayton site environmental monitoring of the aseptic fill lines and other production areas and utility systems. remain in a state of control. Current production levels require that multiple filling activities can occur during any shift and require EM staff to be available to support these activities in order to avoid production delays. | 9/1/2023 |
| 4143 | Grifols Clayton, NC Assistant Biologist/Associate Biologist BS degree in biology, chemistry, or related field. Exp: 6-12 months |
This position is responsible for performing environmental monitoring of fill lines in B300 and SFF and also environmental monitoring of all classified production areas, including sampling of site utility systems. Environmental Assurance department must maintain adequate staffing to support all filling operations 24 hours per day, 7 days a week. In addition to routine environmental monitoring of the aseptic fill lines, this position is also responsible for executing the Quality Oversight program for the fill lines and also provides quality control approval of air flow visualizations conducted on site. This position is part of the budgeted staff necessary to complete this sampling and testing and to ensure that Clayton site environmental monitoring of the aseptic fill lines and other production areas and utility systems remain in a state of control. Must be able to perform tasks by following SOP’s and oral instructions. Must have precise, legible, and organized documentation skills. Candidates must also be willing to perform ones share of cleaning duties and housekeeping. In addition to routine environmental monitoring of the aseptic fill lines, this position is also responsible for executing the Quality Oversight program for the fill lines and also provides quality control approval of air flow visualizations conducted on site. This position is part of the budgeted staff necessary to complete this sampling and testing and to ensure that Clayton site environmental monitoring of the aseptic fill lines and other production areas and utility systems. remain in a state of control. Current production levels require that multiple filling activities can occur during any shift and require EM staff to be available to support these activities in order to avoid production delays | 9/1/2023 |
| 4144 | Grifols Boston, MA Field Service Engineer I Bachelors Degree, Engineering, Technical or related Scientific Discipline. Exp: Entry Level |
The Field Service Engineer will have the primary responsibility of providing the highest quality service and support to Grifols customers at the customer facility and by telephone. This position will be working at customer sites overseeing installations, preventative maintenance, repairs, software and hardware updates. This position will oversee New England, primarily Boston, MA. The ideal individual will have a mechanical or electrical background, have at least 2 years of industry experience working as a Field Service Technician, and previous experience in operating diagnostics equipment in a laboratory environment. | 9/1/2023 |
| 4145 | Grifols Montreal (Canada), CA Automation Engineer M.Sc in Engineering, Automation, Computer, Industrial, Manufacturing or related program. Exp: 1 year |
The Automation Engineer II is a junior level professional who is responsible for using technology to improve and streamline a manufacturing process through automation. Depending on their specific assignment, the incumbent provides automation support for projects or within a specific area, or provides validation support for automation projects. The Automation Engineer II will also integrate into supporting a large scale project. The incumbent is recognized as proficient in her/his field such as specific control systems, instrumentation, process, utilities, or qualification testing. He/she meets customer needs and business goals. In addition, he/she will collaborate with other automation engineers. | 9/1/2023 |
| 4146 | Grifols Clayton, NC Assistant Biologist/Associate Biologist BS degree in biology, chemistry, or related field. Exp: 6-12 months |
This position is responsible for performing environmental monitoring of fill lines in B300 and SFF and also environmental monitoring of all classified production areas, including sampling of site utility systems. Environmental Assurance department must maintain adequate staffing to support all filling operations 24 hours per day, 7 days a week. In addition to routine environmental monitoring of the aseptic fill lines, this position is also responsible for executing the Quality Oversight program for the fill lines and also provides quality control approval of air flow visualizations conducted on site. This position is part of the budgeted staff necessary to complete this sampling and testing and to ensure that Clayton site environmental monitoring of the aseptic fill lines and other production areas and utility systems remain in a state of control. Must be able to perform tasks by following SOP’s and oral instructions. Must have precise, legible, and organized documentation skills. Candidates must also be willing to perform ones share of cleaning duties and housekeeping. In addition to routine environmental monitoring of the aseptic fill lines, this position is also responsible for executing the Quality Oversight program for the fill lines and also provides quality control approval of air flow visualizations conducted on site. This position is part of the budgeted staff necessary to complete this sampling and testing and to ensure that Clayton site environmental monitoring of the aseptic fill lines and other production areas and utility systems. remain in a state of control. Current production levels require that multiple filling activities can occur during any shift and require EM staff to be available to support these activities in order to avoid production delays. | 9/1/2023 |
| 4147 | GlaxoSmithKline Marietta, PA Quality Control Technician B.S. in biology, microbiology, chemistry. Exp: six months |
As Quality Control Technician, you will be responsible for collecting environmental monitoring and utility samples, collecting PEMS data, and performing microbiology testing such as Bioburden and plate reading identification. You will also perform data review for Environmental Monitoring or Microbiology data, perform routine laboratory tasks such as safety shower and eyewash testing, BSC cleaning and stocking, level one audits, daily pH meter and balance calibration, etc, and perform tasks associated with ordering laboratory supplies and maintaining laboratory equipment. | 9/1/2023 |
| 4148 | GlaxoSmithKline Rockville, MD Associate QC Chemist BS Degree in Lifesciences field or Master’s degree in Biochemistry or related field. Exp: 1+ years |
GSK is currently looking for an Associate QC Chemist in Rockville, MD. The Associate QC Chemist performs quality control testing, and data review for biopharmaceutical medicine products. | 9/1/2023 |
| 4149 | GlaxoSmithKline Hamilton, MT QC Analyst 2 Bachelor's Degree in a scientific discipline. Exp: 1+ year(s) |
As a QC Analyst 2 you will perform routine QC laboratory activities to support the manufacture and release of products and incoming materials. Understand test equipment and scientific principles of methods within the scope of their responsibility. | 9/1/2023 |
| 4150 | GlaxoSmithKline Rockville, MD Associate Microbiologist BA/BS in Science field. Exp: 1 year |
GSK currently has an opening for an Associate Microbiologist in Rockville, MD. In this role, you’ll be providing routine QC Microbiology laboratory, with the purpose of meeting daily routine requirements as well as achieving goals established by the manager. | 9/1/2023 |
| 4151 | GlaxoSmithKline Cambridge, MA EHS Associate Bachelor’s degree. Exp: 1+ years |
GSK is currently looking for a EHS Associate to join our team in Cambridge, MA. As an Environment, Health, and Safety Specialist, you will be responsible for providing specialized support and expertise to Binney Street staff in office, laboratory, and manufacturing environments. You will develop, coordinate, and implement environmental, health, and safety training programs with policies and procedures to promote and ensure effective EHS operations in the organization. You will monitor environmental, safety, and health regulations to ensure compliance with federal and state regulations. | 9/1/2023 |
| 4152 | Hillrom Round Lake, IL Research Associate I Bachelors degree in a science-related field. Exp: 0-1 years |
The research we do and the products we develop improve outcomes for patients around the world. As a Research Associate I at Baxter, your work contributes directly to making a significant impact on others. We collaborate cross-functionally and lead by influence. Whether guiding a team through a project or leading teams directly, our research and development team is responsible for influencing others to achieve results! Our colleagues within our R&D organization desire to work on products that make a meaningful difference in others' lives. We are motivated by the power of teamwork and are natural leaders who are skilled at influencing others. When you join Baxter as a Research Associate I, you'll use your analytical approach to identify risks and opportunities for innovation quickly. Agile and willing to take action, you stay calm under pressure! | 9/1/2023 |
| 4153 | ICU Medical San Clemente, CA Engineer I, Product Design - (23300846) Bachelor of Science degree from an accredited college or university in Mechanical Engineering or a related field. Master's Degree preferred.? Exp: 0-2 years |
The Product Design Engineer will support the Business Development R&D department. The engineer is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. The key responsibility of this position is to design, develop, and improve ICU’s product portfolio to ensure their efficiency and reliability. The incumbent will be heavily involved with plastics, polymers, molding, medical disposables, plastics engineering, and solid modeling. The R&D Product Engineer will be expected to interface mainly with internal customers and external suppliers on the design and configuration of high-volume disposable medical devices. The position plays a key role in assisting in the development and compliance challenges involved with new medical devices. The position requires the ability to interact with multiple functional groups such as Marketing, Regulatory, Quality, Operations, etc. | 9/1/2023 |
| 4154 | ICU Medical San Clemente, CA Engineer I, Product Design - (23300845) Bachelor of Science degree from an accredited college or university in Mechanical Engineering or a related field. Master's Degree preferred.? Exp: 0-2 years |
The Product Design Engineer will support the Business Development R&D department. The engineer is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. The key responsibility of this position is to design, develop, and improve ICU’s product portfolio to ensure their efficiency and reliability. The incumbent will be heavily involved with plastics, polymers, molding, medical disposables, plastics engineering, and solid modeling. The R&D Product Engineer will be expected to interface mainly with internal customers and external suppliers on the design and configuration of high-volume disposable medical devices. The position plays a key role in assisting in the development and compliance challenges involved with new medical devices. The position requires the ability to interact with multiple functional groups such as Marketing, Regulatory, Quality, Operations, etc. | 9/1/2023 |
| 4155 | Integrated DNA Technologies SE Bothell, WA Manufacturing Laboratory Technician Bachelor' degree Exp: 0 years' |
The Manufacturing Laboratory Technician is responsible for supporting manufacturing of synthetic oligonucleotides under a cGMP environment for use in Cepheid in-vitro diagnostic products. The position is part of the Oligo Production team and is located in Bothell, WA. At Cepheid, our vision is to be the leading provider in seamlessly connected diagnostic solutions. | 9/1/2023 |
| 4156 | Integrated DNA Technologies SE Bothell, WA Oligonucleotide Manufacturing Chemist BS in Chemistry, Biochemistry preferred. Exp: 0-2 years |
The Oligonucleotide Manufacturing Chemist supports manufacturing of synthetic oligonucleotides under a cGMP environment for use in Cepheid in-vitro diagnostic products. The Chemist will use scientific knowledge and understanding to execute and document standard operating procedures to ensure successful manufacturing and on time delivery of Oligonucleotides. They will contribute to the successful transfer of new products from development to manufacturing ensuring robust manufacturing processes at commercialization and support processes to ensure performance within expected parameters. This position is part of the Oligonucleotide Manufacturing team and will be located onsite in Bothell, Washington facilities. | 9/1/2023 |
| 4157 | Illumina San Diego, CA Engineer 1 - Fluidics Systems B.S. or above in Mechanical Engineering, Bioengineering, Systems Engineering, Applied Physics or related field. Exp: 0 to 2 years |
The Engineer 1 role in Fluidic Systems is part of the Illumina product development team creating new industry-leading genetic analysis platforms for life sciences and clinical markets. You will work in a very interdisciplinary team environment to develop industry-leading genetic analysis instrumentation and device products. Primary responsibilities of this position include design and evaluation of fluidic and microfluidics devices and components in both instruments and consumables, functional spec characterization as it pertains to system-level performance and workflows, critical parameter studies to drive high reliability and robustness, and failure analysis to root cause, mitigation, and permanent correction. You will be responsible for supporting the design, test, and manufacturing transfer of fluidic components, consumables and sub-systems, with a hands-on approach to troubleshooting. This candidate should possess strong organizational and communication skills to facilitate successful product development across instrument, consumables, chemistry, and software teams. | 9/1/2023 |
| 4158 | Cytovance Biologics Oklahoma City, OK QC Stability Associate B.S. in Life Sciences/Chemistry Exp: 1+ Years |
The Stability Associate will participate in the QC Stability Study Program activities which includes designing and drafting stability study protocols according to ICH guidance for drug substance, drug product and reference standard, participate in range of quality control analytical activities such as analytical assay performance, and transfer of standard protein characterization methods. Duties will be carried out in accordance with quality standards and procedures set by the company and applicable government agencies | 8/21/2023 |
| 4159 | Day Zero Diagnostics Boston, MA Associate Bioinformatician Bachelor’s or master’s degree in Computer Science, Bioinformatics, Computational Biology, or a related quantitative field. Exp: Entry Level |
The Associate Bioinformatician will join our Computational Biology team and report directly to a Research Scientist. This person will provide bioinformatics support on R&D projects relating to microbial genomics. Potential projects may include developing bioinformatics pipelines for deployment in MicrohmDB®, our large-scale database of whole genome sequencing data and resistance profiles, or performing bioinformatics analyses that inform updates to Keynome® gAST, our machine learning algorithm used for genomic Antibiotic Susceptibility Testing. This person will have opportunities to work with a world-class database of pathogen genomes and to learn cutting-edge bioinformatics techniques. A strong candidate for this position will be both excited to contribute their knowledge and eager to broaden their skillset to new areas. | 8/21/2023 |
| 4160 | Day Zero Diagnostics Boston, MA Laboratory Research Associate, Sequencing Bachelor's Degree in molecular biology, biochemistry or microbiology. Exp: Entry Level |
PRIMARY RESPONSIBILITIES Perform and assist with sample processing toward diagnostic workflows Strictly follow all lab procedures for specimen handling, processing, and reporting Maintain meticulous documentation of experimental outcomes and observations Work closely with Research Scientists and Associates, and maintain close communication with direct supervisor Repetitive workflows are a frequent occurrence | 8/21/2023 |
| 4161 | DiaCarta Pleasanton, CA Research Associate Sc. degree in molecular biology or a related field. Exp: 0-1 years |
DiaCarta is seeking a highly motivated, independent, and interactive Research Associate to join the R&D function in the company. The new team member will participate in R&D activities with the goal of developing and launching new qPCR, NGS, and branched DNA tests for IVD cancer diagnostics applications. The successful candidate will have outstanding attention to detail, enjoy working in a fast-paced multidisciplinary team environment, and have exceptional hands-on laboratory skills. DiaCarta is a rapidly growing company, so the candidate must be highly motivated and committed to launching their career in an innovative area of molecular diagnostics. This is a full-time role in Richmond, and you will be reporting to the Senior Scientist. | 8/21/2023 |
| 4162 | DiCE Molecules South San Francisco, CA Research Associate/Sr. Research Associate Medicinal Chemistry BS or MS in organic chemistry. Exp: 0-6 years |
We seek an exceptional full-time lab-based synthetic chemistry Research Associate / Senior Research Associate to join our medicinal chemistry team. This individual will be a key contributor to the synthesis of intermediates and final compounds within the goals of developing treatments for inflammatory diseases. Must have legal right to work in US. | 8/21/2023 |
| 4163 | DiscGenics Salt Lake City, UT Manufacturing Associate Bachelor’s degree in related field. Exp: 1+ years |
As DiscGenics prepares to commercialize IDCT, the Manufacturing Associate will be a critical role to execute the daily functions of making IDCT from engineering through commercial production. This role interacts with all levels of the organization in a collaborative and positive way with colleagues to facilitate department and organizational initiatives for cultural cohesion aligned to the DiscGenics Values. | 8/22/2023 |
| 4164 | Distributed Bio Mattawan, MI Research Technician - Second Shift Operations *$1,000 sign on bonus *$20/hr starting wage 1 Bachelor’s/Master’s Exp: 0+ years |
We are seeking a Research Technician for our Second Shift Operations at our Safety Assessment site located Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. | 8/22/2023 |
| 4165 | Distributed Bio Durham, NC Research Technician I Bachelor’s degree (B.A./B.S.) or equivalent in animal science or related discipline. Exp: 1+ years |
We are seeking a Research Technician 1 for our Discovery site located Durham. | 8/22/2023 |
| 4166 | Distributed Bio Mattawan, MI Research Analyst I- Formulations Bachelor’s/Master’s degree in a relevant field. Exp: 0+ years |
We are seeking a Research Analyst I for our Test Material Control/Formulations Department site located Mattawan, MI. A Research Analyst I - Test Material Control (TMC)/Formulations is responsible for: preparing, sampling, and dispensing formulated test material according to applicable Standard Operating Procedures (SOPs) and GxP guidelines. The individual in this role: completes projects on time while maintaining quality and efficiency; communicates effectively with management, internal customers, and team members; assists others with their duties; and may assist with troubleshooting formulation issues. | 8/22/2023 |
| 4167 | Distributed Bio Durham, NC Research Technician I Bachelor’s degree (B.A./B.S.) or equivalent in animal science or related discipline. Exp: 1+ years |
We are seeking a Research Technician I for our Discovery site located Durham. | 8/22/2023 |
| 4168 | Distributed Bio Worcester, MA Research Technician I Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months |
We have an exciting opportunity for a Research Technician 1 at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. | 8/22/2023 |
| 4169 | Distributed Bio Worcester, MA Research Technician I Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months |
We have an exciting opportunity for a Research Technician 1 at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. | 8/22/2023 |
| 4170 | Distributed Bio Mattawan, MI Research Analyst 1 - Discovery Bioanalytical BS/BA in relevant field. Exp: 0-2 years |
We are seeking a Research Analyst 1 for our Discovery Bioanalytical Chemistry Team in Mattawan MI. Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP’s and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents. | 8/22/2023 |
| 4171 | Earli Redwood City, CA Temporary Research Associate or Senior Research Associate, Cell Biology BS or MS degree in Life Sciences or Cell Biology or Immunology. Exp: 1-2 years |
Earli, Inc. is currently seeking a dynamic Senior/Research Associate who is inspired to change the world by pushing the scientific envelope. | 8/22/2023 |
| 4172 | Earli Redwood City, CA Temporary Senior Research Associate - LNP Formulation Bachelors or Masters degree in biology, chemistry, or life sciences (STEM) Exp: 0 – 1 year |
Earli is seeking a highly motivated and ambitious Senior Research Associate interested in pursuing a career in biotech. The candidate will gain hands-on experience in lipid nanoparticle formulation and characterization, learn about LNP design, and be part of a supportive team. The main responsibility for this role is to provide small scale formulations for in vivo studies. The candidate should have basic hands-on experience working in a biology or chemistry lab and be a highly responsible and reliable individual. The candidate should be comfortable working in a fast-paced environment and excited to contribute to Earli’s mission. | 8/22/2023 |
| 4173 | Exponential Business & Technologies Eden Prairie, MN Nano Analytical and Testing Lab Technician BE or BS degree in Materials Science and Engineering, Mechanical Engineering, Physics, Chemistry or related disciplines. Exp: One to two years |
Ebatco is seeking an energetic, self-disciplined, customer service oriented technical person to join its Nano Analytical and Testing Laboratory (NAT Lab). As a technical member of the NAT Lab team, the technician performs contract lab services and instrument demonstrations with appropriate levels of support and supervision, operates advanced nano/micro scale scientific instruments, collects testing and measurement data, and writes technical report on experimental results and observations. | 8/22/2023 |
| 4174 | Editas Medicine Waltham, MA Cell Manufacturing Associate - 2259 Bachelor’s degree in Life Sciences/Engineering field. Exp: 0-2 years |
Key Responsibilities & Accountabilities: Perform duties as dictated by standard operating procedures (SOPs) for cellular product manufacturing and under GxP guidelines as directed. Work in a clean room environment while fully gowned following GMP guidelines and using aseptic technique. Work in a Biological Safety Cabinet for open processing operations. Operate instrumentation needed for cell manufacturing. Accurately complete batch record documentation, all appropriate equipment log entries, and GMP documentation. Maintain orderly lab space. Maintain sufficient inventory of supplies and reagents for performance of duties. Clean and maintain laboratory equipment in good working order. Prepare solutions and culture media as appropriate. Work in compliance with all appropriate laboratory regulatory and safety requirements. | 8/22/2023 |
| 4175 | EMD Serono Sheboygan Falls, WI Associate Production Scientist - 12 Hour Night Shift Bachelor’s Degree in Chemistry, Chemical Engineering, or other life science discipline. Exp: 0+ years |
$7k sign-on bonus for this position The Associate Production Scientist at MilliporeSigma will manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department.$7k sign-on bonus for this position The Associate Production Scientist at MilliporeSigma will manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. | 8/23/2023 |
| 4176 | EMD Serono St. Louis, MO Associate Production Scientist - 2nd Shift Bachelor’s Degree in Chemistry, Biochemistry, Chemical Engineering, Biology or STEM degree. Exp: 1 + years |
MilliporeSigma has an opening at the St. Louis - Broadway site as a 2nd Shift Associate Production Scientist! In this role you will lead the group and assist the Supervisor and other departments to meet the manufacturing department needs. 2nd shift hours are from 2:00pm to 10:30pm Monday-Friday. | 8/23/2023 |
| 4177 | EMD Serono Miamisburg, OH Associate Production Scientist Bachelor’s Degree in Chemistry Exp: 0+ years |
At MilliporeSigma the Associate Production Scientist will manufacture or evaluate products according to established protocols, provide technical support to others, and perform operations in support of the group and department. He/she will safely perform operations to meet quality expectations ensuring quality throughout the process. The Associate Production Scientist must also complete the volume of work required to achieve group/departmental goals and meet deadlines. Participation in quality audits will be required as needed. In compliance with change control procedures, he/she will also be responsible for improving processes through application of scientific knowledge, experience, and principles. | 8/23/2023 |
| 4178 | EMD Serono Sheboygan Falls, WI Associate Production Scientist - 12 Hour Night Shift Bachelor’s Degree in Chemistry, Chemical Engineering, or other life science discipline. Exp: 0+ years |
*$7,000 Sign-On Bonus for 12 hour Night Shifts* Paid after 90 days of employment Your Role: As an Associate Production Scientist at MilliporeSigma, you will manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department* | 8/23/2023 |
| 4179 | EMD Serono Rocklin, CA Production Lab Tech 1 Undergraduate Degree in Chemistry, Biochemistry, or other life science discipline Exp: 0+ years |
MilliporeSigma in Rocklin, CA is hiring a Production Lab Tech 1. The position is responsible for all tasks related to Production and Warehouse duties. This individual will work independently with a high level of attention to detail and in accordance with GMP regulations. | 8/23/2023 |
| 4180 | EMD Serono Sheboygan Falls, WI Associate Production Scientist - Night Shift Bachelor’s Degree in Chemistry, Chemical Engineering, Biochemistry or other life science discipline Exp: 0+ years |
*$7,000 Sign-On Bonus for this 12 hour Night Shift* Paid out after 90 days of employment Your Role: The Associate Production Scientist at MilliporeSigma in Sheboygan Falls, WI, will manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. | 8/23/2023 |
| 4181 | EMD Serono Sheboygan Falls, WI Associate Production Scientist - 3rd Shift Bachelor’s Degree in Chemistry, Chemical Engineering, Biochemistry, or other life science discipline Exp: 0+ years |
The Associate Production Scientist at MilliporeSigma in Sheboygan Falls, WI, will manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. | 8/23/2023 |
| 4182 | Endo Pharmaceuticals Rochester, MI Chemist II (Afternoon Shift) Master’s Degree in chemistry, chemical engineering or related field. Exp: 1+ years’ |
The Chemist II, under general supervision, performs QC laboratory chemical analyses of raw materials, in-process materials, stability & finished products, and testing to support process validation. Detects, participates and reports on OOS/OOT/NOE and other investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. May train less senior staff. | 8/23/2023 |
| 4183 | Endo Pharmaceuticals Rochester, MI Validation Engineer I Bachelor of Science in Engineering or Science discipline preferred Exp: Zero (0) to three (3) years |
The Validation Engineer I evaluates and performs specified validations leading to the accurate and reliable validation of products, processes, equipment, facilities, and systems; assists/performs development of studies/cycles for new processes; helps troubleshoot product problems related to validation; performs testing and documents results for review by site, corporate and government review. Further responsible for providing supporting protocol rationales/justifications for the chosen validation methodology/approach. Participates in programs to achieve departmental objectives. Records and reports results. Notes unusual results and notifies management for evaluation. Assists with writing validation documents. | 8/23/2023 |
| 4184 | Endo Pharmaceuticals Rochester, MI Quality Associate Specialist, Product Release - Midnight Shift BA/BS degree in a related discipline. Exp: 0-1 year |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. | 8/23/2023 |
| 4185 | Exosome Diagnostics Waltham, MA Medical Laboratory Technologist Bachelor of Science Degree in a chemical, physical or biological science. Exp: six months |
This position is responsible for performing high-complexity CLIA testing in day-to-day operations of the laboratory. | 8/24/2023 |
| 4186 | FORMA Therapeutics Lexington, MA Research Associate - Chemistry Bachelors or Masters in Chemistry or related field. Exp: 1-3 years |
Dicerna Pharmaceuticals is seeking a highly motivated Research Associate with a strong background in synthetic and medicinal chemistry to join the Chemistry Team. The candidate will be responsible for the synthesis of oligonucleotide conjugates, nucleoside analogues, small molecule ligands, and linkers. This position will contribute to the development of novel nucleic acid conjugate platforms and support therapeutic programs in multiple disease areas. The Dicerna research team will provide an exciting learning opportunity and a collaborative and fast-paced research environment. | 8/25/2023 |
| 4187 | FORMA Therapeutics Fremont, CA Engineer I Bachelor Degree within subject matter expertise preferred. Exp: 0- 1+ years’ |
The Engineer I will make significant contributions to the research of life changing medical devices at Novo Nordisk (NN). They leverage their strong background in engineering to perform their individual tasks as well as energetically engaging in collaborative work. The Engineer I will contribute to insert subject matter expertise. They ensure strong progress on research initiatives under the broad direction of more senior engineers and management. | 8/25/2023 |
| 4188 | FORMA Therapeutics West Lebanon, NH Cell Therapy Lab Technician Bachelor’s degree in Cell Biology, Molecular Biology, or a closely related field required. Exp: One (1) year |
This position has the responsibility of working with associates and scientists to execute laboratory scale process development or validation studies in support of manufacturing development, or process troubleshooting, or scale-up. This position is located in West Lebanon, New Hampshire and will require onsite work and collabortation. It is a full time (40 hours per week) position and the standard schedule is Monday-Friday (8am-5pm), with weekends based on business needs. | 8/25/2023 |
| 4189 | FORMA Therapeutics West Lebanon, NH Manufacturing Science and Analytical Technology Associate I Bachelor’s degree or equivalent in Biochemistry, Chemistry, Engineering or a closely related field. Exp: one year |
This position has the responsibility of working with senior level Scientists to execute laboratory scale process development or validation studies in support of process or assay development, or process troubleshooting or scale-up. The scientific knowledge in this position will range from familiarity with details of manufacturing process, process chemistries, development studies and relevant assay methods and instruments. This position will be one of the interfaces between Manufacturing Science and Analytical Technology (MSAT) and Manufacturing or Quality. | 8/25/2023 |
| 4190 | FORMA Therapeutics West Lebanon, NH Manufacturing Technician - Night Shift Bachelors’ Degree in a science discipline. Exp: zero (0) years’ |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. With the growth of our site, we are seeking night shift support. We offer the following shift schedules that include a 15% shift differential: 7:00pm-7:00am (everyother week has 8-hours built in overtime): Sunday-Tuesday and everyother Saturday Wednesday-Friday and everyother Saturday | 8/25/2023 |
| 4191 | FORMA Therapeutics West Lebanon, NH Manufacturing Technician Bachelors’ Degree in a science discipline. Exp: zero (0) years’ |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. We offer both day and night shifts positions (schedule below). With the growth of our site, we are seeking night shift support. Day Shift (7:00am-7:00pm) : Sun-Tuesday everyother Wedneday Thur-Saturday everyother Wednesday Night Shift (7:00pm-7:00am- includes 15% shift differential): Sunday-Tuesday everyother Saturday Wednesday-Friday everyother Saturday | 8/25/2023 |
| 4192 | FORMA Therapeutics Clayton, NC Quality Assurance Area Specialist I or II Bachelor’s Degree (or equivalent) required, a scientific discipline preferred. Exp: one (1) year |
This position will reviews manufacturing and support documentation and records to certify compliance with in-house specifications/standards and GMP for all NNUSBPI products. This position has QA signature authority on the review of individual batch records, supporting test records and other ancillary support records. Will assist in the internal audit program and be a QA presence on the manufacturing floor. | 8/25/2023 |
| 4193 | Fresenius Kabi Melrose Park & Chicago, IL Manufacturing Engineer Bachelor’s degree in Engineering (Electrical, Chemical, Controls, Computer, Mechanical, etc.). Exp: 1-3 years |
The Manufacturing Engineer will use technical expertise in support of daily operations in aseptic filling or formulation by defining, measuring, analyzing, coordinating, implementing and follow-up concerning projects and activities designed to increase or improve safety, quality, productivity, and/or capacity. Apply accepted engineering practices and project management techniques to assigned daily tasks and projects. Analyze situations, break them down into key components and milestones, conduct fact-finding missions, provide detailed plans of action, and implement plans as assigned. | 8/25/2023 |
| 4194 | Fresenius Kabi Melrose Park & Chicago, IL Associate Scientist (Nights) BS/BA degree in Science or related field. Exp: 0+ years |
The Associate Scientist will be responsible for collection and testing of routine environmental monitoring samples within aseptic processing fill lines, Isolator fill line, compounding, sterility suite, and component preparation areas for aseptic lines (Building A) and clean rooms areas in new expansion Building B. Collect and test utility samples such as WFI, clean steam and compressed gases. Monitors environmental conditions in laboratory areas during test sessions. Reports testing results and documents in compliance with cGMP and GLP standards. Provides support to Scientist, Lead Scientist, and Supervisor. Prepares media, reagents, sanitizing solutions and equipment for use in testing. | 8/25/2023 |
| 4195 | Fresenius Kabi Grand Island, NY SCIENTIST (Chemistry) - 3rd Shift B.S. in Chemistry, Biology, or related physical science. Exp: 1-4 years |
3rd Shift is 10 PM to 6:30 AM, Monday through Friday nights. This position starts between $28.46 - $34.00/hour. A Scientist I in Quality Control is responsible for an intermediate level of expertise in analytical chemistry, chromatographic methods of analysis and instrumentation, including troubleshooting. Directs and provides guidance to associate scientists. | 8/25/2023 |
| 4196 | Fresenius Kabi Grand Island, NY ASSOCIATE SCIENTIST - 2nd Shift Chemistry B.S. in Chemistry, Biology, or related physical science. Exp: 0-2 years |
This position pays between $22.76 - $23.76/hour. An Associate Scientist is responsible for performing entry level chemical testing to support raw material, in-process, stability, and finished products as required for Quality Control. Effectively communicates work and results both orally and in writing. | 8/25/2023 |
| 4197 | Fresenius Kabi Grand Island, NY ASSOCIATE SCIENTIST - 1st Shift Chemistry B.S. in Chemistry, Biology, or related physical science. Exp: 0-2 years |
An Associate Scientist is responsible for performing entry level chemical testing to support raw material, in-process, stability, and finished products as required for Quality Control. Effectively communicates work and results both orally and in writing. | 8/25/2023 |
| 4198 | Catalog Boston, MA Mechatronics Engineer BS in Mechatronics, Mechanical, Electrical, or a related engineering field. An advanced degree is a plus. Exp: Entry Level |
We are seeking a dynamic Mechatronics Engineer to join our multidisciplinary team. We are pushing the boundaries of science and technology, and you can help make the difference. This position, while guided by the Mechanical Engineering team, will work closely with Biology and Computer Science groups in our quest to develop next-generation DNA writing technology. We're looking for someone who can turn an idea from a brainstorming session into a proof-of-concept test system through background research, project plan development, custom test equipment design, experimental prototype building, code writing for test automation, and experimental data analysis. | 8/15/2023 |
| 4199 | Catalog Boston, MA Research Associate or Senior Research Associate, DNA Computing BS or MS in biology, molecular biology, biochemistry, or a related discipline. Exp: Entry Level |
We are actively seeking a Research Associate or Senior Research Associate with a solid grounding in molecular biology or chemistry. In this role, you'll be instrumental in helping to build CATALOG's innovative DNA-based data storage and computation platform. You'll collaborate with our dynamic team of computer scientists and biologists, developing novel storage and computing architectures and translating them into scalable chemical operations. Your work will contribute to the optimization of a molecular instruction set that underpins the world’s first DNA storage and computing platform. | 8/15/2023 |
| 4200 | Cenetron Diagnostics Indianapolis, IN Associate Technologist Laboratory- 4 x 10s, Sat-Tues 8pm to 630am, rotating holidays Bachelor's Degree from an accredited college or university in biology, chemistry, molecular biology, immunology, clinical laboratory science, medical Exp: 1+ years |
Under direct supervision by department leadership, performs CLIA regulated and clinical contract research testing. Interacts at a basic level with customers, providing a high level of customer service to resolve customer concerns about sample acceptability and results. Supports preparation of laboratory reagents and routine maintenance of laboratory equipment . | 8/15/2023 |
| 4201 | Cenetron Diagnostics Milwaukee, WI Technologist Laboratory- Hemostasis Bachelor's Degree from an accredited college or university in biology, chemistry, molecular biology, immunology, clinical laboratory science, medical Exp: 1-3 years |
Under supervision by department leadership, performs CLIA regulated and clinical contract research testing. Interacts with customers, providing a high level of customer service to resolve customer concerns about sample acceptability and results. Supports preparation of laboratory reagents and routine maintenance of laboratory equipment. Supports the training of junior and peer staff members. Performs higher level interpretation of testing results and test panels. | 8/15/2023 |
| 4202 | Cenetron Diagnostics Wauwatosa, WI Research Technologist - Dr. Dipa Lab Bachelor's Degree from an accredited college or university in biology, chemistry, scientific discipline or equivalent combination of education and exp Exp: 1-3 years |
Under the direction of the Principal Investigator, performs laboratory assays and complex experiments to elucidate novel research questions. | 8/15/2023 |
| 4203 | Cenetron Diagnostics Wauwatosa, WI Research Technologist II - Flow Cytometry Core Lab Bachelor's Degree from an accredited college or university in biology, chemistry or equivalent scientific discipline required. Master's Degree preferr Exp: 1-3 years |
Under the direction of the Director, Core Laboratories develops, improves, and implements laboratory techniques and performs complex experiments or tests to contribute to the timely and accurate completion of research project(s) that involve flow cytometry. Works with Senior Coordinator Flow Cytometry Laboratory to provide the expertise and resources needed to contribute significantly to research projects that require fluorescence activated cell sorting and/or analysis. Stays current with information relative to the field of flow cytometry and the research being performed in the VBRI Flow Cytometry Core Lab. The successful candidate will have 1 or more years of flow cytometry experience and have demonstrated ability in flow cytometry techniques | 8/15/2023 |
| 4204 | Cenetron Diagnostics Indianapolis, IN Associate Technologist Laboratory- to Wed-Sat 8PM to 430AM w/ rotating holidays Bachelor's Degree from an accredited college or university in biology, chemistry, molecular biology, immunology, clinical laboratory science, medical Exp: 1+ years |
Under direct supervision by department leadership, performs CLIA regulated and clinical contract research testing. Interacts at a basic level with customers, providing a high level of customer service to resolve customer concerns about sample acceptability and results. Supports preparation of laboratory reagents and routine maintenance of laboratory equipment . | 8/15/2023 |
| 4205 | Cenetron Diagnostics Wauwatosa, WI Research Technologist - Histology Bachelor's Degree from an accredited college or university in biology, chemistry or equivalent scientific discipline required. Master's Degree preferr Exp: 1-3 years |
Position requires a bachelor’s degree or equivalent and demonstrated experience in research histology. Completion of an accredited histotechnology program is desired but not required. This position will report to the Director of VBRI Core Laboratories. | 8/15/2023 |
| 4206 | Champions Oncology Rockville, MD Research Technician I, Surgical Services BS degree in animal science, biology, pharmacology, or related field. Exp: 1 year |
Job Overview Support in vivo oncology research studies in mice as a member of the Surgical Services Team. Duties and Responsibilities: Perform survival surgical procedures on mice, including handling, restraint, tumor volume measurement with calipers or imaging device, anesthesia, surgical heterotopic tumor fragment and tumor cell implantations, euthanasia, tissue collection, and tissue cryopreservation. Record study data within the laboratory information management system. Read, understand, and adhere to study protocols. Perform general study preparation and organizational activities, including sample tube labeling, supply organization and stocking, and laboratory organization. Work weekends and holidays on rotating basis | 8/16/2023 |
| 4207 | Cisbio Annapolis, MD Research Technician II - Cell Culture Bachelor of Science degree. Exp: 6 months |
Responsibilities: Serves as subject matter expert for the Cell Services Research Technicians Assists Research Tech Supervisor in delegation of daily tasks and management of the Inventory Specialist team Provide high quality laboratory support to the Cell Services team. Grow, maintain, and cryopreserve contamination-free mammalian cells (suspension & adherent). Preparation of cell pellets for histological processing. Provide daily, vials of tested, frozen cell lines to scientists. Isolate and cryopreserve primary PBMCs and further cell subsets from both whole blood and leukopaks. Isolate a variety of cell types from fresh blood daily in a timely manner. Isolate serum from whole blood. Maintain sterile technique while culturing isolated primary cells. | 8/16/2023 |
| 4208 | Cisbio Annapolis, MD CCFS Media Prep Technician Bachelor Degree in a chemistry, biology, or other relevant discipline. Exp: 0-1 year |
Responsibilities: Work with Cell Culture and Fermentation Suite scientists to prepare cell culture media, feed, stocks, buffers and reagents Primary duties will include preparing many types of biological cell culture basal media, nutrient feed and stock solutions for NS0, CHO and hybridoma cells Solutions will be tested for osmolarity, pH, and turbidity Using aseptic technique and a biological safety cabinet, filter or pump solution into sterile containers as requested by scientists and store all solutions properly Lab instrument maintenance for Nova, Cedex, BGA, pH meter and osmometer as schedule permits Monitor stock solution inventory and prepare as needed Label all solutions according to CCFS guidelines | 8/16/2023 |
| 4209 | Cisbio Annapolis, MD Research Technician - Cell Culture Bachelors Degree in science or chemistry. Exp: 6 months |
Responsibilities: Provide high quality laboratory support to the Cell Services team. Grow, maintain, and cryopreserve contamination-free mammalian cells (suspension & adherent). Preparation of cell pellets for histological processing. Provide daily, vials of tested, frozen cell lines to scientists. Isolate and cryopreserve primary PBMCs and further cell subsets from both whole blood and leukopaks. Isolate a variety of cell types from fresh blood daily in a timely manner. Isolate serum from whole blood. Maintain sterile technique while culturing isolated primary cells. Perform established flow cytometry QC protocols on a routine basis and analyze results. | 8/16/2023 |
| 4210 | Cisbio Annapolis, MD Research Technician - Cell Culture Bachelors Degree in science or chemistry. Exp: 6 months |
Responsibilities: Provide high quality laboratory support to the Cell Services team. Grow, maintain, and cryopreserve contamination-free mammalian cells (suspension & adherent). Preparation of cell pellets for histological processing. Provide daily, vials of tested, frozen cell lines to scientists. Isolate and cryopreserve primary PBMCs and further cell subsets from both whole blood and leukopaks. Isolate a variety of cell types from fresh blood daily in a timely manner. Isolate serum from whole blood. Maintain sterile technique while culturing isolated primary cells. Perform established flow cytometry QC protocols on a routine basis and analyze results. | 8/16/2023 |
| 4211 | Cisbio Annapolis, MD Research Technician - Cell Culture Bachelors Degree in science or chemistry. Exp: 6 months |
Responsibilities: Provide high quality laboratory support to the Cell Services team. Grow, maintain, and cryopreserve contamination-free mammalian cells (suspension & adherent). Preparation of cell pellets for histological processing. Provide daily, vials of tested, frozen cell lines to scientists. Isolate and cryopreserve primary PBMCs and further cell subsets from both whole blood and leukopaks. Isolate a variety of cell types from fresh blood daily in a timely manner. Isolate serum from whole blood. Maintain sterile technique while culturing isolated primary cells. Perform established flow cytometry QC protocols on a routine basis and analyze results. Generate and analyze data with the highest Data Integrity standards to include identifying and reporting unusual results/outcomes. Operate and maintain laboratory instrumentation including Mycoplasma onsite testing & clean-up as warranted. | 8/16/2023 |
| 4212 | Cognate Bioservices Mattawan, MI Research Technician - Second Shift Operations *$1,000 sign on bonus *$20/hr starting wage 1 Bachelor’s/Master’s Exp: 0 years |
We are seeking a Research Technician for our Second Shift Operations at our Safety Assessment site located Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives | 8/18/2023 |
| 4213 | Cognate Bioservices Mattawan, MI Research Analyst I- Formulations Bachelor’s/Master’s degree in a relevant field. Exp: 0 years |
We are seeking a Research Analyst I for our Test Material Control/Formulations Department site located Mattawan, MI. A Research Analyst I - Test Material Control (TMC)/Formulations is responsible for: preparing, sampling, and dispensing formulated test material according to applicable Standard Operating Procedures (SOPs) and GxP guidelines. The individual in this role: completes projects on time while maintaining quality and efficiency; communicates effectively with management, internal customers, and team members; assists others with their duties; and may assist with troubleshooting formulation issues. The pay range for this position is $23.50/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. The shift is for the weekend, Friday to Monday 6 AM-2:30 PM but will train for the first 12 weeks Monday-Friday 6 AM-2:30 PM. When you work Saturday or Sunday there will be a 10% shift differential. | 8/18/2023 |
| 4214 | Cognate Bioservices Durham, NC Research Technician I Bachelor’s degree (B.A./B.S.) or equivalent in animal science or related discipline. Exp: 1+ years |
We are seeking a Research Technician 1 for our Discovery site located Durham. The following are responsibilities related to the Research Technician 1: • Perform routine research activities as assigned, including in vivo-based screens. • Perform dosing of laboratory animals, animal husbandry. • Prepare & verify dosing solutions for administration. • Ensure that all individual study supplies are on-site & prepared in a timely manner. • Perform equipment maintenance. • Review protocol with manager to insure proper study execution. • Prepare & organize study data, study folders & data forms; perform data collection and entry. • Review study report, gives feedback on the accuracy of the materials & methods section; report data to more senior staff. The pay for this position is $24/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. | 8/18/2023 |
| 4215 | Cognate Bioservices Mattawan, MI Research Analyst I- Flow Cytometry Bachelor’s degree (BA/BS) Exp: 0 years |
We are seeking a Research Analyst I for our Flow Cytometry Team at our Safety Assessment site located in Mattawan, MI. Biomarkers (and Investigative Pathology) personnel are responsible for: The development, performance, and support of biomarkers and flow cytometry-based assays. Assisting in sample analysis for both the support of internal studies as well as external client-based studies in a GLP compliant environment. Including, but not limited to cytokine, hormone, renal, cardiovascular, osteo, complement, metabolic, and inflammatory markers. | 8/18/2023 |
| 4216 | Cognate Bioservices Mattawan, MI Research Analyst I - Immunochemistry Bachelor's degree (BA/BS) Exp: 0 years |
The Immunology and Immunochemistry disciplines support large molecule drug development using ligand binding assays (LBA), such as enzyme-linked immunosorbent assay (ELISA), to measure large molecules and their immune responses. The main types of assays include Pharmacokinetic (PK) assays to measure drug and Immunogenicity assay to measure anti-drug antibodies (ADA) and neutralizing antibodies (NAb). Other assay types also performed are branched DNA (bDNA) and cell-based assays. An array of platforms are used to support these assays that include spectrophotometer, Meso Scale Discovery (MSD), Luminex and Gyrolab. Utilizing these platforms/assays, the teams are responsible for the method development, validation and routine sample analysis in both the regulated and non-regulated space of non-clinical and clinical studies. | 8/18/2023 |
| 4217 | Cognate Bioservices Mattawan, MI Research Analyst II, Discovery Bioanalytical 1 BS/BA in relevant field Exp: 1 year |
Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP’s and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents. | 8/18/2023 |
| 4218 | Companion Medical Memphis, TN R-D Engineer I Bachelors Mechanical Engineering or Technically degree required. Exp: 0 years |
As a R&D Engineer I, you will design and develop life-saving medical device products. Key responsibilities include leading new product development, conducting product testing and creating models and prototypes. You will actively seek out Voice of the Customer (VOC) input and translate that into product requirements, design specifications, and mechanical concepts. You will work under general direction and may serve as key functional core team member and/or leadership role in an extended team. The product focus will be on spinal implants and instrumentation to treat degenerative, deformity, and tumor/trauma conditions. | 8/18/2023 |
| 4219 | Companion Medical Memphis, TN R-D Engineer II Advanced degree Mechanical Engineering Exp: 0 years |
As a R&D Engineer II, you will design and develop life-saving medical device products. Key responsibilities include leading new product development, conducting product testing and creating models and prototypes. You will actively seek out Voice of the Customer (VOC) input and translate that into product requirements, design specifications, and mechanical concepts. You will work under general direction and may serve as key functional core team member and/or leadership role in an extended team. The product focus will be on spinal implants and instrumentation to treat degenerative, deformity, and tumor/trauma conditions. | 8/18/2023 |
| 4220 | Cook Biotech Bloomington, IN Manufacturing Engineer Bachelor’s Degree in Engineering. A degree in Mechanical, Electrical, Production, or Manufacturing Engineering preferred. Exp: 1+ years |
The Manufacturing Engineer 1 plans, directs, and coordinates manufacturing processes for medical device products, and supports Operations in a way to assure a quality product is produced in a timely manner. The Production Engineer works with Operations, Quality Assurance and Regulatory Affairs to improve existing product designs and processes to increase throughput, decrease operational costs, or improve quality. | 8/18/2023 |
| 4221 | Cook Biotech Vandergrift, PA Manufacturing Engineer 1 Bachelor’s Degree in Mechanical, Electrical, Production, or Manufacturing Engineering, or related field. Exp: 1+ years |
The Manufacturing Engineer primarily plans, directs, and coordinates manufacturing processes for medical device products, and supports Operations in a way to assure aquality product is produced in a timely manner, in addition to performing sustaining activities for commercially available products The Manufacturing Engineer works with Operations, Quality Assurance and Regulatory Affairs to improve existing product designs and processes to increase throughput, decrease operational costs, and improve quality while ensuring products and processes meet regulatory compliance. | 8/18/2023 |
| 4222 | Cooper Surgical Portland, OR Laboratory Technician 1 Bachelor's degree in Science. Exp: one to two years |
Executes an array of SOPs to screen, process, and preserve semen samples for future clinical use. This position is part of a dynamic laboratory system that includes primarily lab bench work and cryogenic procedures. This position works with multiple cross functional teams to achieve the best possible outcomes for the populations we serve. | 8/18/2023 |
| 4223 | Cooper Surgical New York, NY Laboratory Technician 1 - Evening Shift Bachelor's degree in a science field i.e. Biology, General Science, chemistry, etc. Exp: one to two years |
Performs routine semen banking procedures by performing the following duties. | 8/18/2023 |
| 4224 | Cooper Surgical New York, NY Laboratory Technician 1 - Evening Shift Bachelor's degree in a science field i.e. Biology, General Science, chemistry, etc. Exp: one to two years |
Performs routine semen banking procedures by performing the following duties. | 8/18/2023 |
| 4225 | Cooper Surgical New York, NY Laboratory Technician 1 - Evening Shift Bachelor's degree in a science field i.e. Biology, General Science, chemistry, etc. Exp: one to two years |
Performs routine semen banking procedures by performing the following duties. | 8/18/2023 |
| 4226 | Cooper Surgical Los Angeles, CA Laboratory Technician 1 - Evening Shift Bachelor's degree in Science. Exp: one to two years |
Executes an array of SOPs to screen, process, and preserve semen samples for future clinical use. This position is part of a dynamic laboratory system that includes primarily lab bench work and cryogenic procedures. This position works with multiple cross functional teams to achieve the best possible outcomes for the populations we serve. | 8/18/2023 |
| 4227 | Cooper Surgical Los Angeles, CA Laboratory Technician 1 - Evening Shift Bachelor's degree in Science. Exp: one to two years |
Executes an array of SOPs to screen, process, and preserve semen samples for future clinical use. This position is part of a dynamic laboratory system that includes primarily lab bench work and cryogenic procedures. This position works with multiple cross functional teams to achieve the best possible outcomes for the populations we serve. | 8/18/2023 |
| 4228 | Cooper Surgical Los Angeles, CA Laboratory Technician 1 - Evening Shift Bachelor's degree in Science. Exp: one to two years |
Executes an array of SOPs to screen, process, and preserve semen samples for future clinical use. This position is part of a dynamic laboratory system that includes primarily lab bench work and cryogenic procedures. This position works with multiple cross functional teams to achieve the best possible outcomes for the populations we serve. | 8/18/2023 |
| 4229 | CordenPharma Boulder, CO Chemical Process Engineer BS in Chemical Engineering Exp: 1 year |
Performs research and development activities for the purpose of transferring and designing/improving a process or technology. Provides process engineering support for manufacturing processes in assigned group or plant through developing and implementing continuous improvements. And through troubleshooting methods and equipment used in the production of bulk pharmaceutical intermediates and active pharmaceutical ingredients. | 8/18/2023 |
| 4230 | CordenPharma Boulder, CO QC Analyst - Nights Bachelor's Degree (BA) from 4-year college or university. Exp: 0+ years |
Performs all technician tasks accurately and efficiently without supervision. Initiates expert technical advice to customers and completes all tasks in the Technician Training Manual. Maintains a high level of housekeeping and attention to detail. | 8/18/2023 |
| 4231 | CryoLife Kennesaw, GA Process Engineer I (onsite) Bachelor’s degree in Engineering (Mechanical, Chemical, Biomedical, Industrial or related field of engineering). Exp: 0-2 years |
Responsible for providing process engineering support for all product manufacturing departments. Supports manufacturing operations to ensure consistent adherence to the standard operating procedures and business continuity. Initiates process improvement initiatives to improve the efficiency of current manufacturing processes, as well as develop new processes to improve manufacturing efficiency. Supports new product launches by collaborating with other functional areas and providing process engineering expertise during the implementation of processes or equipment. | 8/18/2023 |
| 4232 | CryoLife Kennesaw, GA Lab Assurance Associate - Microbiology Record Review Bachelor’s Degree in the Life Sciences or an equivalent field of study preferred. Exp: 1+ years |
The Lab Assurance Associate will assist management in the review of Microbiology records to ensure they are compliant with required Standard Operating Procedures. Will ensure that all areas outlined under “Principal Responsibilities” are accomplished in an efficient, professional manner. | 8/18/2023 |
| 4233 | CSL Behring Waltham, MA Scientific Associate I (Protein Biochemistry) Bachelor or Master’s degree in Biochemistry or related biological sciences. Exp: BS: 1-3+ years; MS: 0-1+ years |
This position is responsible for the production and characterization of high quality purified recombinant protein of potential vaccine candidates. The ideal candidate would support development of cell cultures for expression of vaccine antigens and carries out protein purifications and characterizations. | 8/18/2023 |
| 4234 | Curi Bio Seattle, WA Laboratory Technician Bachelor’s degree in a scientific field is required. Exp: 1+ years |
Curi Bio is a rapidly growing startup company seeking a Laboratory Technician to join our team to perform cellular medium production, quality control and shipping/logistics. Prioritized candidates will have experience in aseptic cell culture, prior biotech experience, and experience with standard cell biology assays. Experience in quality control/assurance functions and/or logistics in a biotech atmosphere is highly desired. | 8/18/2023 |
| 4235 | Cyprotex Framingham, MA Research Associate BS/ MS in a relevant bio scientific discipline. Exp: 0-2 years |
The team is looking for a highly motivated Research Associate and/or Research Assistant that will be responsible for routine screening of compounds in various in vitro toxicology assays. | 8/18/2023 |
| 4236 | Cyprotex Rahway, NJ Research Associate B.S./M.S. in Molecular Biology, Synthetic Biology, Bioengineering, Biochemistry, or a related field. Exp: 1+ years |
There is an immediate opening for a motivated Research Associate to join the Reagents team in Evotec US. Evotec Reagents is a growing business unit delivering high quality materials to the pharmaceutical and agrochemical industry. Driven by business demand, our group was launched in Q1 2015 and is rapidly expanding, requiring suitable candidates to join this flagship operation. | 8/18/2023 |
| 4237 | Cyprotex Princeton, NJ Research Associate BS/BA in biology, biochemistry, engineering, or related scientific discipline Exp: 1-3 years |
The Assay Operations Group is seeking a talented and innovative Research Associate (full-time/permanent position) to join our growing team at Evotec’s US headquarters in Princeton, New Jersey. The successful candidate will join the Sample Management Group and provide assay automation support along with basic compound management support for the Assay Group. | 8/18/2023 |
| 4238 | Lonza Houston, TX Core Tech Viral Vector/Cell Therapy, BS or AA Life Sciences Exp: 0-1 year |
Responsible for aseptic processing of clinical grade product, participates in editing SOPs and batch records, maintains and stocks clean room environment with released inventory, monitors temperatures, expiration of materials and calibrated equipment; Supports cleanroom environment maintenance at below alert limits by following established cleaning practice; Packages kits, blood tubes and final product for shipment and monitors expiry of critical raw materials as needed; Complies with processes, procedures and instructions for all activities in which the team participates according to written guidelines and recognizes deviations from accepted practice; Responsible for carrying out production processes in a GMP facility, with tasks including cell culture | 08/15/23 |
| 4239 | Biodesix Boulder, CO Laboratory Technician II Bachelor’s degree in a chemical, physical, biological, or clinical laboratory science or medical technology • OR equivalent laboratory training and ex Exp: 1+ years |
Laboratory Technicians II assist with the setup and support of the daily activities of the laboratory. In addition, Laboratory Technicians II have the technical training and experience required to perform regulated clinical laboratory test realization (test specimen receipt through test result generation) using standard in-vitro laboratory techniques in Molecular Biology (PCR) and in Mass Spectrometry. Our focus areas of test development include oncology and virology. This experienced candidate is comfortable with SOPs and Work Instructions, working with data, standard laboratory chemicals, human blood specimens and is versed in standard molecular biology techniques (PCR, nucleic acid isolation/purification and sequencing). The position also works in a functional matrix organization, including Development, Customer Service, Accounting, Quality Operations management team, the Laboratory Directors, and other departments as needed. Ongoing training will be provided to supplement key skills required to perform the functions of this position as applicable. | 8/7/2023 |
| 4240 | Biodesix De Soto, KS Laboratory Technician I Bachelor’s degree in a chemical, physical, biological, or clinical laboratory science or medical technology; or equivalent laboratory training and exp Exp: 1+ years |
The Laboratory Technician I assists with the setup, support, and execution of the daily activities of the laboratory. In addition, a Laboratory Technician I will have the technical training and experience required to perform regulated clinical laboratory test realization (i.e., test specimen receipt through test result generation) using standard in-vitro laboratory techniques. Team members are also expected to operate a proprietary LIMS. The position also operates in a cross-functional matrix organization working across departments, including Development, Customer Service, Accounting, Quality, Operations, the Laboratory Directors, and other departments as needed. Ongoing training will be provided to supplement key skills required to perform the functions of this position as applicable. Required: must embrace a culture of transparency, willing and open to share data and technical knowledge, excellent communication skills, on time delivery of complete and quality results. Communicates issues promptly to manager with follow through to a resolution. Qualified Laboratory Technicians may act as responsible delegates according to the Biodesix Quality Matrix, including day to day responsibilities required for CAP/CLIA as well as all state-specific requirements in which Biodesix is an approved test facility. | 8/7/2023 |
| 4241 | Biogen Research Triangle Park, NC Manufacturing Associate (Recent Grad/Entry Level) – Upstream & Downstream Bachelor’s Degree (STEM preferred). Exp: Entry-Level |
Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; with two main areas/disciplines – Upstream (Cell Culture) and Downstream (Purification). MAs perform these critical steps within Current Good Manufacturing Practice (cGMP) biosafety cabinets and cleanroom suites. | 8/7/2023 |
| 4242 | Biogen Research Triangle Park, NC Manufacturing Associate II, Oral Solid Dose Bachelor’s Degree (STEM preferred). Exp: Entry-Level |
Manufacturing Associates perform processing steps and manufacturing support activities in our facilities in Research Triangle Park (RTP). These teams are the backbone of our operations – each person playing a critical role in delivering our therapies to the patients who need them. This position will be in our Oral Solid Dose area, and our teams operate across the following units: Dispensing, Blending, & Milling Compression Coating Encapsulation | 8/7/2023 |
| 4243 | Biogen Research Triangle Park, NC Manufacturing Associate III - Parenteral Filling Bachelor’s Degree (STEM preferred). Exp: 6 months |
Manufacturing Associates perform processing steps and manufacturing support activities in our facilities in Research Triangle Park (RTP). These teams are the backbone of our operations – each person playing a critical role in delivering our therapies to the patients who need them. This position will be in our Parenteral Filling area, and our teams operate across the following units: Component Preparation Compounding Parenteral Filling/Lyophilization Visual Inspection | 8/7/2023 |
| 4244 | BioLegend San Diego, CA QC Development Research Associate Bachelor’s degree in a scientific discipline (preferably biology) Exp: 0 – 2 years |
At BioLegend, we are dedicated to commercializing high quality reagents to support the life science community for legendary discoveries that lead to cure. This position will contribute to improved QC assay development for current and new GMP bioprocessing products. The main GMP bioprocessing products are biologically active recombinant proteins, antibodies and cell culture media. The main responsibilities include performing studies and experiments to develop, optimize and validate the QC assay for launching new specifications for existing and new GMP bioprocessing products. In addition, He/She will assist with troubleshooting and contribute ideas to support product testing, assay improvement and on critical projects. The position also requires working closely with Product Development, Manufacturing, routine QC and QA teams to establish or modify assay SOPs. Additional responsibilities include generating and presenting data summaries, providing ETAs, and helping train others on experimental protocols and assisting with data review. We are looking for a highly motivated person who loves science and wants to be part of a dynamic and fast paced team. | 8/7/2023 |
| 4245 | BioLegend San Diego, CA Research Associate I - Cell Analysis Bachelor's in a Life Science related area. Exp: 1+ years |
The Research Associate I - Cell Analysis will be involved in product and reagent development for cell separation related applications. This position will have the opportunity to independently drive research projects from conception to completion, and will interact with multi-disciplinary teams. | 8/7/2023 |
| 4246 | Bioqual Rockville, MD Research Associate II BS/ MS in Life Science or similar field. Exp: 1+ years |
Ability to work with the Lab Supervisor to generate study related documents, and perform procedures including drug material formulation, challenge inoculum, treatments/therapeutics. Organized and detail oriented, especially would maintain detailed records on experimentation and reagent/ sample inventories. Good communication skills and a team player. Ability to multi-task with high level attention to details. Perform other duties as assigned. | 8/7/2023 |
| 4247 | Bioqual Rockville, MD Research Associate I BS in a related field Exp: 0-5 years |
The Research Associate I, under specific direction, performs a variety of basic and general laboratory research and clerical tasks determined by the field and scope of the particular research study. May perform tasks related to the research project independently, but within specific guidelines and subject to review by supervisor or other research staff. The Research Associate I is responsible for conducting in vitro experiments in order to produce reliable and precise data to support scientific investigations. The Research Associate I should be familiar with the SOPs relating to the laboratory for which they take responsibility for carrying out routine tasks accurately and following strict methodologies to perform a variety of analyses. They must have experience in laboratory techniques that are supportive of the intended research provided in approved protocol. | 8/7/2023 |
| 4248 | BioReliance Sheboygan Falls, WI Associate Production Scientist - 12 Hour Night Shift Bachelor’s Degree in Chemistry, Chemical Engineering, or other life science discipline. Exp: 0+ years |
*$7,000 Sign-On Bonus for 12 hour Night Shifts* Paid after 90 days of employment Your Role: As an Associate Production Scientist at MilliporeSigma, you will manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department Perform operations to meet quality expectations throughout the process Perform routine assays, processes and/or unit operations Complete the volume of work required to achieve group/departmental goals and meet deadlines Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal) Communicate the status of operations and bring deviations to the attention of supervisor Provide complete and accurate records consistent with quality guidelines Ensure all applicable logbooks have been filled out completely as required by current procedures Interact with other departments as needed | 8/8/2023 |
| 4249 | BioReliance Rocklin, CA Production Lab Tech 1 Undergraduate Degree in Chemistry, Biochemistry, or other life science discipline Exp: 1+ years |
MilliporeSigma in Rocklin, CA is hiring a Production Lab Tech 1. The position is responsible for all tasks related to Production and Warehouse duties. This individual will work independently with a high level of attention to detail and in accordance with GMP regulations. | 8/8/2023 |
| 4250 | LGC Biosearch Technologies Petaluma, CA Quality Control Analyst I Bachelor’s degree in a relevant field such as Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or other directly related field. Exp: 1 years |
The Quality Control (QC) Analyst I focuses on the performance of analytical and functional testing activities within the QC chemistry lab. They are responsible for testing intermediate and finished chemical products, analysing the results of the QC testing and comparing results to established specification and customer requirements. In addition, they perform testing and/or review of incoming goods. This position reports to the Quality Control Supervisor or Quality Control Manger. This position requires a thorough understanding of basic laboratory etiquette, laboratory safety and chemical competency. This position will offer an in-depth understanding of the Quality Control process while additionally expanding knowledge of general analytical laboratory equipment such as the use of an HPLC, Spectrophotometer, and DNA synthesizers. | 8/8/2023 |
| 4251 | LGC Biosearch Technologies Petaluma, CA Oligonucleotide Production Technician I Bachelors Degree or Master's Degree preferred in Life Sciences. Exp: 0-2 years |
The Oligonucleotide Production Technician I will perform tasks associated with the production of modified oligonucleotides in a high throughput, fast paced, and time sensitive manufacturing environment. This position focuses within the Oligonucleotide Synthesis department. | 8/8/2023 |
| 4252 | Bio-techne Minneapolis, MN Quality Control Technician Position requires an MLT/MLS degree, Bachelor’s degree in Biology, or related field of study. Exp: 0-1 year |
This position will require setup, maintenance, troubleshooting, and operation of QC hematology analyzers. This position will require monitoring instrument performance throughout the QC process and troubleshooting the instrument when necessary. This position will test hematology products for homogeneity during the bottling process by following established methods. The expectation for this position is to setup and QC product on 50% of the laboratory instruments and troubleshoot as necessary. Other tasks include proofing labels and assay sheets. This position will adhere to safety regulations. Perform additional duties as assigned. | 8/8/2023 |
| 4253 | Bio-techne Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
This position is responsible for the developing and or formulation of standards, controls, calibrators, and intermediates in the production and development of Bio-Techne's Luminex, Q-kit, DuoSet, and Simple Plex product lines. Day to day responsibilities involve hands on work in a production laboratory running assays for ELISA and Luminex. You will draft and revise standard operating procedures, manage a production schedule, and analyze assay data to further the ongoing development of new and existing products within Bio-Techne’s evolving portfolio. | 8/8/2023 |
| 4254 | Bio-techne Minneapolis, MN Advanced Quality Assurance Specialist Master's degree in a biological or chemical scientific discipline. Exp: up to 2 years |
As an Advanced Quality Assurance (QA) Specialist you will support the quality functions of BioTechne through quality systems development and improvement, document and records review, auditing, and other quality functions. The Advanced QA Specialist will understand and follow appropriate quality procedures to meet compliance standards, including ISO 9001, ISO 13485, 21CFR11, and 21CFR820. This position will be responsible for supporting the Immunoassay Business Unit focusing on the Luminex product line. | 8/8/2023 |
| 4255 | Bio-techne Minneapolis, MN Research Associate, Antibody Applications B.S. degree in Biochemistry, Chemistry, Biology, or a related field. Exp: 0 - 2 years |
The Research Associate is responsible for routine quality control testing of antibodies using immunohistochemistry (IHC) and immunocytochemistery (ICC). The testing includes culturing and handling of stem cells, primary cells, and basic cell lines for the use in ICC. The handling of fixed tissues for use in IHC. The position requires routine documentation, data analysis and good communication of results. | 8/8/2023 |
| 4256 | Bio-techne Minneapolis, MN Research Associate, Analytical QC B.S. degree in Biochemistry, Chemistry, Biology, or a related field. Exp: 0 - 2 years |
As the Research Associate, Analytical Quality Control Analyst you will perform routine quality control testing of protein, peptide or antibody products using standard operating procedures to determine lot status, product release and product stability. Tests include concentration determination, SDS-PAGE with densitometry, endotoxin assay, PCR, HABA, conductivity, total organic carbon and other testing as assigned. Participation in the validation of new and existing laboratory methods is also expected. The position requires routine documentation, analysis, and communication of results within the department and across different groups. Other duties include instrument calibration and maintenance, record keeping, and lab support. Within this job function, the Research Associate must also pursue annual goals that aim to facilitate innovation, efficiency, productivity, and team building across the QC Department or the entire company. Perform additional duties as assigned. | 8/8/2023 |
| 4257 | Bio-techne Wallingford, CT Quality Technician Bachelor of Science degree in relevant field. Exp: 0-2 years’ |
The Quality Technician role is established to support the Simple Plex Consumables team in the Wallingford facility. Assists Quality Analysts and the QA team in our ISO compliant environment. Provides support for QC / QA activities including: hands-on evaluation of microfluidic cartridge products. $22.00 to $25.00 per hour based on experience and qualifications | 8/8/2023 |
| 4258 | Bio-techne Austin, TX Advanced Research Associate Master’s degree in biology, molecular biology, biochemistry, genetics, or similar fields . Exp: 0-2 years |
Advanced Research Associates in our Research Group develop innovative nucleic acid technologies. This role will support new product initiatives by combining novel, highly multiplexed PCR technologies with analysis platforms such as qPCR, digital PCR, and long-read sequencing, and by integrating reagents, instrumentation, analysis algorithms, and software. Diagnostic disease applications span neurogenetics, (such as myotonic dystrophy, fragile X and autism spectrum disorder), oncology (liquid and solid tumors), carrier screening and other reproductive health applications. You will work in a cross-functional team to develop products and technologies that realize the next generation of molecular diagnostic tests. | 8/8/2023 |
| 4259 | bluebird bio Somerville, MA Associate Scientist II, Vector Process Development (Contract) MS in Bioengineering, Chemical engineering, Biology, Virology, Cell or Vector Biology or related biological sciences. Exp: 1+ years |
You’ll help to bring more patients their bluebird days by: Executing viral vector production experiments to assess the impact of process improvements and/or new technologies. All aspects of upstream and downstream viral vector production including mammalian cell culture, media preparation, culture initiation, seed train maintenance, transfection, filtration, and chromatography. Performing complex technical analytical work related to viral vector production, including cell-based assays, ELISA, flow cytometry and RT-PCR. Developing experimental plans, interpreting scientific results, providing statistical analysis where appropriate, summarizing and presenting scientific data and report progress on behalf of the team under the guidance of the senior scientists. Performing general laboratory tasks, including maintenance of equipment and inventory. Generating, managing, evaluating, and maintaining critical data in a highly organized manner including lab notebook maintenance with good documentation practices. | 8/9/2023 |
| 4260 | Camber Spine King of Prussia, PA Associate Project Engineer Bachelor’s degree in Mechanical Engineering (preferred), Biomedical Engineering, or other relevant technical discipline. Exp: 0-3 years |
The Associate Project Engineer will be involved with legacy and new product projects, including project planning, execution, while adhering closely to project timeline and budget | 8/10/2023 |
| 4261 | Cambrex Longmont, CO Associate Analytical Scientist II/III (QC) Associate Analytical Scientist II (QC): BS/MS in chemistry, biochemistry, or similar science-related field. Exp: 1+ years |
We are looking for a quality control chemist capable of testing all common analytical methodologies. This individual will have the ability to execute analytical methods as needed and is able to organize routine work with minimal instruction from management and accurately evaluate and interpret generated data. This individual will demonstrate an understanding of compliance as related to the analytical laboratory. | 8/10/2023 |
| 4262 | Cambrex Agawam, MA Analytical Analyst I Bachelor’s Degree (or advanced degree) in Chemistry or related science field required. Exp: 1+ years |
Analytical Analysts are responsible for a variety of daily Analytical laboratory operations to meet established testing requirements and turnaround time commitments to our medical device, pharmaceutical and biotechnology customers. | 8/10/2023 |
| 4263 | Advanced Sterilization Products Spring House, PA Associate Scientist I, CAR Screening Master’s degree in Life Sciences (e.g. Biology, Biotechnology) or a related field. Exp: 1-2 years |
The Cell Therapy team at Janssen Therapeutics Discovery is seeking a highly motivated lab-based Associate Scientist to join our Chimeric Antigen Receptor (CAR) Screening and Discovery team. The Associate Scientist I will join a cross-functional group of experts building a high throughput CAR screening pipeline for autologous and iPSC-derived effector cell types. The ideal candidate is an organized, self-driven scientist that thrives in a collaborative team-based environment, is excited to learn and has experience setting up in vitro functional assays to measure T cell function using both representative cell lines and primary human cells. Key activities will include performing in-vitro functional assays for large scale screening of CAR candidates, immune cell phenotyping through multi-color flow cytometry & cell line maintenance. Any experience in immunology, cell therapy and/or immuno-oncology is a plus but not required. | 8/10/2023 |
| 4264 | Advanced Sterilization Products Spring House, PA Associate Scientist, Downstream Process Development (Cell and Gene Therapy) Master’s Degree in Chemical Engineering, Biomedical Engineering, Biological Science, or related field. Exp: 1 year |
The candidate for this position will take the role of leading the downstream process development for the viral/ vaccine process scale-up and tech transfer within the Cell and Gene Therapy group in Spring House, PA. The primary responsibilities will include assisting in planning and designing of downstream experiments, leading the team towards successful execution of the planned experiments, optimize the process steps to improve or enhance the quality attributes of the molecule. | 8/10/2023 |
| 4265 | Advanced Sterilization Products Danvers, MA Product Development Engineer Cardiology BS in Mechanical, Biomedical Engineering or directly related scientific discipline. Exp: 1+ years |
The Cardiology Platform (Impella CP and Impella RP) is focused on rapidly developing the next-generation of percutaneously implanted Impella cardiac pumps. We are a dynamic development team that drives innovative solutions to improve patient care. As a Product Development Engineer you will support and own technical efforts, design initiatives, and engineering activities for next generation Impella systems. You’ll have a tangible impact on our business and be rewarded by a positive impact to patients' lives. | 8/10/2023 |
| 4266 | Advanced Sterilization Products Raynham, MA Quality Engineer Bachelor’s or equivalent University degree is required, recent graduates will still be considered. Exp: 1 year |
The Quality Engineer I should excel in an environment that embraces teamwork, change, risk-based decision-making, and flexibility. This individual will work in a design team setting. This individual will support design control activities for new product development. They will also support quality deliverables and tasks for commercialized devices on an as required basis. | 8/10/2023 |
| 4267 | Caris Life Sciences Phoenix, AZ Clinical Engineering Technician, Molecular Operations - Solid Tumor (3rd Shift) Bachelors or Master’s degree in a science field. Exp: one year |
The Clinical Engineering Technician is responsible for the organization, installation, and maintenance of the equipment within the clinical molecular lab. | 8/10/2023 |
| 4268 | Caris Life Sciences Phoenix, AZ Quality Assurance Technologist, Molecular - Liquid Profiling (2nd Shift) Bachelor’s degree in a science field. Exp: 1+ year |
A Quality Assurance Technologist is responsible for a multitude of different tasks within the clinical molecular laboratory including the quality control testing of all molecular reagents prior to use on clinical samples, assisting the product development team with the validation of new assays and training current employees on new assays as well as new employees on established assays. This position is required to be well versed in various molecular techniques that include, formalin-fixed paraffin-embedded tissue macro-dissection, RNA/DNA extractions, PCR, RFLP, DNA methylation analysis, Next Generation sequencing and automated liquid handlers. Quality Assurance Technologists are expected to contribute technically and intellectually to enhance efficiency within the lab while ensuring that the quality of reagents and training program is maintained to the highest standard. This position works under the direction of the Director and follows standard laboratory procedures and policies. | 8/10/2023 |
| 4269 | Caris Life Sciences Phoenix, AZ Molecular Technologist - Liquid Profiling (3rd Shift) Bachelor’s degree in a science field is required. Exp: 1+ years |
The Molecular Technologist – Liquid Profiling is responsible for performing various molecular techniques that include, but are not limited to, blood processing and buffy coat extraction, RNA/DNA extractions, PCR, DNA methylation analysis, Next-Generation Sequencing, equipment maintenance, laboratory inventory, sample tracking and receiving packages. This position works under the direction of the supervisor and follows standard laboratory procedures and policies. | 8/10/2023 |
| 4270 | Caris Life Sciences Phoenix, AZ Molecular Technologist - Liquid Profiling (2nd Shift) Bachelor’s degree in a science field is required. Exp: 1+ years |
The Molecular Technologist – Liquid Profiling is responsible for performing various molecular techniques that include, but are not limited to, blood processing and buffy coat extraction, RNA/DNA extractions, PCR, DNA methylation analysis, Next-Generation Sequencing, equipment maintenance, laboratory inventory, sample tracking and receiving packages. This position works under the direction of the supervisor and follows standard laboratory procedures and policies. | 8/10/2023 |
| 4271 | Caris Life Sciences Phoenix, AZ Molecular Technologist, Solid Tumor (2nd Shift) Bachelor’s degree in a science related field. Exp: Less than 1 year |
The Molecular Technologist I is responsible for performing various molecular techniques that include, but are not limited to, formalin-fixed paraffin-embedded tissue macro-dissection, RNA/DNA extractions, PCR, DNA methylation analysis, equipment maintenance, laboratory inventory, sample tracking, ordering supplies and receiving packages. This position works under the direction of the supervisor and follows standard laboratory procedures and policies. | 8/10/2023 |
| 4272 | Caris Life Sciences Phoenix, AZ Reagent QC Specialist I - Molecular Bachelor’s degree in a scientific field is required. Exp: 1+ years’ |
The Reagent QC Specialist I – Molecular is responsible for maintaining compliance to all applicable regulatory requirements pertaining to the QC process for all incoming reagents which includes initial inspection upon receipt, performing applicable verification testing and assessment, and review of final QC paperwork before passing on to Process Quality for final reagent release into the laboratory. | 8/10/2023 |
| 4273 | Catalent Baltimore, MD Associate Scientist II, Cell Culture and Cell Line Development MS degree in a biological discipline (biochemistry, molecular biology, cell biology or equivalent). Exp: 1-3 years |
Reporting to a Senior Scientist for daily supervision, the Associate Scientist II – Cell-culture Innovation and Product development will work independently as well as collaboratively within our growing team in Biopark, MD. The individual should bring technical knowledge, initiative, strong scientific integrity, and an enthusiasm for learning to make measurable contributions within the group. | 8/10/2023 |
| 4274 | Catalent Greenville, NC Analytical Chemist I Bachelor’s degree a science-related discipline (e.g. Biology, Chemistry, Pharmaceutical Sciences). Exp: 0+ years |
Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. The Analytical Chemist I primarily performs routine analytical testing in support of pharmaceutical products following all applicable safety, quality, and regulation requirements. | 8/10/2023 |
| 4275 | Catalent Bloomington, IN Associate Scientist - QC Bachelor’s degree in science field OR Master’s degree in science field. Exp: BS: 0-3 years; MS: 0-2 years |
The Quality Control (QC) team is responsible for testing products, raw materials, and the manufacturing environment to ensure the safety, quality, identity, purity, and potency produced by the facility. The QC team is comprised of the following groups: microbiology, environmental monitoring, stability, release and in-process, method validation, sample management, raw materials, and other functions. This position requires a variety of skills necessary for biotech company operations. The position will perform routine testing of process samples, raw materials, finished products and stability samples, while adhering to SOPs and working in a cGMP compliant environment. The position will analyze and interpret results in written and oral format. Additionally, this position will support preventative maintenance and basic laboratory maintenance activities while maintaining a GMP quality system. Other duties will include data review/archiving, database entry/review, and contributions to process improvement initiatives. This is a permanent, full time position. It is a salaried role. The shift is Friday-Sunday 6:00am-6:30 pm. | 8/10/2023 |
| 4276 | Catalent Madison, WI Lab Associate, Upstream Process Development B.S/B.A. in Biotechnology, or related field. Exp: 1+ years |
The Upstream Process Development team is responsible for the development and implementation of upstream processing methodologies and analytical procedures that can be easily transferred to the cGMP Manufacturing Team. The Lab Associate, Upstream Process Development will perform a variety of laboratory procedures to support Upstream Process Development. The position will perform daily work assignments accurately and in a timely and safe manner. The Lab Associate, Upstream Process Development will perform routine scientific work, evaluating, selecting and applying standardized scientific procedures and techniques to assignments with clear, specific objectives; assignments require investigation of a limited number of variables and few complex features. Limited exercise of judgment is required on details of work and in making preliminary selections and adaptations of alternatives. This is a fulltime role working 8AM – 5PM Days; Monday – Friday | 8/10/2023 |
| 4277 | Catalent Madison, WI Assistant Scientist, Analytical Development B.S/B.A. in any STEM discipline. Exp: 0+ years |
The Analytical Development team is responsible for evaluating client analytical methods and/or optimizing/developing methods required to support cell line, upstream, and downstream development, and transferring them to the QC department for phase appropriate validation. The team is also responsible for characterizing primary and high order structures; confirming product comparability across scale and establishing product degradant profiles and specifications for reference standards of mRNA proteins/mAbs generated at Catalent’s, Madison site. The team executes on this by applying the concepts of analytical quality by design (AQbD) in compliance with FDA and other regulatory agency requirements and in conformance with the sites GMP quality systems. The team’s role is therefore central to the success of projects that enter cell line and process development and technology transfer workstreams and also ensures that analytical methods can be applied in establishing product critical quality attributes (CQA) and supporting IND-enabling studies and applications that are essential in providing high quality drug products for our clients and their patients. This is a full-time on-site hourly position, Monday - Friday 8:00am to 5:00pm CST. Please Note: This role may require some weekend shift work to support business need. | 8/10/2023 |
| 4278 | Catalent St Petersburg, FL Associate Scientist, QC BS or BA with college course work in related sciences. Exp: 1+ years |
The Associate Scientist II, QC will independently test, develop and implement assays useful for the identification and characterization of Raw Materials, pre-capsulation, Stability and Finished Products. Analyze data, document results, maintain laboratory notebook according to cGMP and Internal guidelines. The Associate Scientist II, QC communicate results in written and oral presentations. Help in writing Procedures, Specifications and Test Methods. Keep abreast of literature in field; help train colleagues; contribute to continuous improvement within the group. Comply with FDA, EPA and OSHA regulations, performing all work in a safe manner. Maintain proper records in accordance with all SOP's and policies. | 8/11/2023 |
| 4279 | Norwich Pharmaceuticals Norwich, NY Chemist I BS in Chemistry, Biochemistry, Microbiology or Biology or related discipline. Exp: 0-3 years |
The Quality Control Chemist I / Microbiologist I: Performs routine testing to assess the conformance of raw materials, finished products, and/or stability samples to predetermined product specifications. Performs routine testing in conformance with approved procedures, accurately and concisely documents data, and reports results. Demonstrates a basic knowledge of SOP’s and GMP regulations as related to the pharmaceutical quality control laboratory | 8/2/2023 |
| 4280 | AnaSpec Fremont, CA Synthesis Chemist I BS or above in Chemistry, Organic Chemistry, or related disciplines. Exp: 1-3 years |
The Synthesis Chemist I will perform peptide production and conduct in-process testing using Good Laboratory Practices (GLP). As a member of the Synthesis department, the Synthesis Chemist I will work closely with the Purification, QC, and Sales & Business Development departments. | 8/2/2023 |
| 4281 | ANI Pharmaceuticals Baudette, MN QC Chemist/Sr. QC Chemist Bachelors degree in chemistry, biochemistry, microbiology or closely related field/major. Exp: QC Chemist – 1-3 years |
The QC Chemist position is responsible for independently performing testing in a pharmaceutical Quality Control laboratory. All work will be conducted in accordance with standard operating procedures and test methods. This includes performing testing on raw material, in-process and finished product samples. Execute compendia method validations, method transfers and validation support of new product development. Set up and confirm suitable operation of equipment and instrumentation. Collect data and generate/report results in accordance with governing test methods and SOPs. | 8/3/2023 |
| 4282 | Applied Medical Rancho Santa Margarita, CA Electrical Engineer I Bachelor’s degree in Electrical Engineering, Biomedical Engineering, Computer Engineering with an emphasis in Electrical Engineering or equivalent. Exp: 1+ years |
As an Engineer I (Sustaining/Manufacturing Electrical Engineer) you will be responsible for working within the framework of a team to provide engineering support to medical device development projects from design through production phase. You will be expected to design, investigate, develop, and qualify new manufacturing processes, fixtures, and equipment. Along with writing test protocols and reports, conducting various testing, collecting, and analyzing data and trends. | 8/4/2023 |
| 4283 | Applied Medical Rancho Santa Margarita, CA Biocompatibility & Sterilization Reporting Analyst Bachelor's Degree?in physical or biological sciences. Exp: 1+ years |
The Biocompatibility & Sterilization Reporting Analyst will support activities relating to the Biological Sciences team and its associated laboratories. Responsibilities will include coordinating all testing activities for bioburden, sterility, biocompatibility or other testing programs requiring outside services from a third-party laboratory. Testing will include both routine audits as well as R&D projects. You must be capable of writing protocols and final test reports and ensuring compliance with relevant standards, regulations, and guidance documents. | 8/4/2023 |
| 4284 | Applied Medical Rancho Santa Margarita, CA Quality Systems Engineer I/II – Test Method Validation Bachelor's Degree or higher in Engineering or a scientific field. Exp: one years' |
As an Engineer I/II on the Quality Systems (QS) Team, you will be responsible for working within the framework of a team and performing the following activities: Enhance product quality by developing and validating test methods that check for product performance and effectiveness Work closely with the Product and Process Development teams to understand user needs, design and process requirements and test method acceptance criteria Develop clear and testable methods using technical standards and engineering principles Design and create required test equipment | 8/4/2023 |
| 4285 | Applied Medical Rancho Santa Margarita, CA Process Engineer II/III Bachelor’s degree in Mechanical, Biomedical, Industrial, or Manufacturing Engineering (or equivalent). Exp: 1-4 years |
As a Process Engineer, you will work within the Group Process Development team and use skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. The Process Engineer’s primary responsibilities are debugging, observing, and expediting shop orders. You will assist with developing and updating engineering documents and investigating new tooling, materials, manufacturing processes, and technologies. | 8/4/2023 |
| 4286 | Applied Medical Rancho Santa Margarita, CA Quality Engineer I Bachelor’s degree in an Engineering or Science, Technology, Engineering, and Mathematics (STEM) field or related education and experience. Exp: 1+ years |
As a Quality Engineer I, you will learn and develop skills to support medical device quality through design controls, process validations and documentation as part of a cross-functional team. | 8/4/2023 |
| 4287 | Applied Medical Rancho Santa Margarita, CA Plastics Process Engineer II Bachelor’s degree in Polymer, Materials, Plastics, or Manufacturing Engineering (or equivalent). Exp: 1-2 years |
As a Plastics Process Engineer II, you will use skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. | 8/4/2023 |
| 4288 | Applied Medical Rancho Santa Margarita, CA Mechanical Engineer, Automation 4-year degree in Mechanical Engineering or in a related field. Exp: 1 year |
As a Design Engineer, you will play a vital role in supporting the development of automated machines or automated processes for our in-house medical device manufacturing. Below are some of the common skills and qualities that are sought after for this role. | 8/4/2023 |
| 4289 | Aquinnah Pharmaceuticals Cambridge, MA Research Associate Master’s degree in neuroscience, cell biology or related discipline. Exp: 1+ years |
The successful candidate should be highly motivated, flexible and enjoy working in a team - based environment with a strong interest in contributing to the discovery of new therapies for the treatment of neurodegenerative disease. This position is laboratory-based and requires strong experimental skills with a background in cell biology, molecular biology, or biochemistry. Under supervision, the candidate will assist in duties including, but not limited to: cell culture maintenance, compound screening, biochemical assays, immunocytochemistry, and analysis using state of the art high-content imaging. Strong communication skills are required including the ability to analyze and report on the results. The candidate will be expected to function efficiently and cooperatively within a team and maintain accurate and clear project records. The ideal candidate will be creative, energetic and motivated. Candidates should have a Bachelor’s or Master’s degree in neuroscience, biology, or related field. Salary will be competitive and commensurate with experience. | 8/4/2023 |
| 4290 | Arraystar Rockville, MD Lab Assistant - Molecular Biology Bachelor’s degree in a relevant biological field. Exp: 1-2 years’ |
Responsibilities: Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. Assist with the generation and updating of laboratory SOPs. Perform basic lab maintenance tasks such as ordering lab supplies, and keeping detailed lab records. Communicate with clients to obtain/verify information of their projects, orders or requests. | 8/4/2023 |
| 4291 | Astute Medical Salt Lake City, UT Research Associate I Bachelor’s degree in a scientific discipline. Exp: six months’ |
The Research Associate I (RA I) works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g., nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to communicate and coordinate with peers and supervisor(s) effectively and respectfully. | 8/4/2023 |
| 4292 | Astute Medical Saint Louis, MO Associate Mechanical Engineer Bachelor's Degree in Mechanical Engineering or a related engineering discipline. Exp: 0 years’ |
This is a mechanical design engineering position with an emphasis on engineering design of complex medical instruments. This individual will collaborate with R&D engineering staff to design, document, prototype, and test complex medical instruments. | 8/4/2023 |
| 4293 | Astute Medical San Jose, CA V&V Microbiologist Bachelors Degree in microbiology or related science discipline. Exp: one year |
Specific is seeking a Verification and Validation (V&V) Microbiologist with experience in Research and Development. You will be a key contributor and critical to the success of the company. As part of the V&V team, you will be responsible for testing, documenting, and evaluating instruments and consumables to support the company’s product lines. You will be responsible for writing specifications, testing protocols, and processes that ensure that test materials/products are reliable and repeatable. As part of the Microbiology team, you will help build up toward commercial readiness of our products and will execute laboratory functions as listed below. | 8/4/2023 |
| 4294 | Astute Medical Salt Lake City, UT Template Control Laboratory Technologist I B.S. in chemistry, biology, or a related field. Exp: 6 months |
The Template Control Laboratory Technologist (LT) works with a team that formulates DNA and RNA template control components to support the company’s in vitro diagnostic products’ research and development, manufacturing, validations, and quality control efforts. The LT-I will use established methods and techniques to maintain the lab’s DNA and RNA template inventory, perform template manipulations and verification including diluting, aliquoting, mixing, quantitative PCR, quantitative RT-PCR, and FilmArray analysis, perform template and control mix formulations, and dispense template and control mixes to dependent departments in accordance with the company’s quality system. | 8/4/2023 |
| 4295 | Astute Medical Salt Lake City, UT Template Control Laboratory Technologist I B.S. in chemistry, biology, or a related field. Exp: 6 months |
The Template Control Laboratory Technologist (LT) works with a team that formulates DNA and RNA template control components to support the company’s in vitro diagnostic products’ research and development, manufacturing, validations, and quality control efforts. The LT-I will use established methods and techniques to maintain the lab’s DNA and RNA template inventory, perform template manipulations and verification including diluting, aliquoting, mixing, quantitative PCR, quantitative RT-PCR, and FilmArray analysis, perform template and control mix formulations, and dispense template and control mixes to dependent departments in accordance with the company’s quality system. | 8/4/2023 |
| 4296 | Astute Medical Salt Lake City, UT Research Associate I Bachelor's degree in a scientific discipline. Exp: six months’ |
The Research Associate I (RA I) works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g., nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to communicate and coordinate with peers and supervisor(s) effectively and respectfully. The position requires basic laboratory technical skills, organizational skills, attention to detail, critical thinking, troubleshooting and problem-solving, and a dedication to the mission and goals of the department and bioMérieux. A Research Associate I may receive general or detailed instruction and direct supervision on general work, new procedures, and assignments. | 8/4/2023 |
| 4297 | Astute Medical Salt Lake City, UT Research Associate I Bachelor’s degree in a scientific discipline. Exp: entry-level |
This is a full time non-exempt position. This position is part of a team working on a variety of laboratory procedures involving real-time PCR using established methods and techniques under general guidance. Performs general lab duties, designs and conducts experiments, collects and analysis data and keeps an accurate record of all work done in accordance with the quality system. Requires some problem solving skills. Normally receives general instructions on routine work, detailed instruction on new assignments. Reports to the System Validation Manager. | 8/4/2023 |
| 4298 | Atalanta Therapeutics Boston, MA Associate Scientist I/II, In Vitro Biology Master’s degree in biochemistry or relevant biological science. Exp: 0-2 years |
Atalanta is seeking a highly motivated individual to join our In Vitro Biology team to contribute to the preclinical development of RNAi-based therapeutics. The selected individual will design and execute biochemical assays for the quantification of therapeutic oligonucleotides and contribute towards their profiling of pharmacokinetic properties. The Associate Scientist will be responsible for supporting multiple drug development programs for neurodegenerative diseases. This is an ideal position for candidates who thrive in a team-oriented, fast-paced, and cross-disciplinary environment. | 8/4/2023 |
| 4299 | Atalanta Therapeutics Boston, MA Associate Scientist II/Senior Associate Scientist, siRNA Screening Master’s degree in biochemistry or relevant biological science. Exp: 0-2 plus years |
Atalanta Therapeutics is seeking an experienced and highly motivated Associate Scientist II or Senior Associate Scientist to be part of the dynamic and collaborative In Vitro Biology team. This individual will contribute to cell-based screening of therapeutic oligonucleotides under direction of the HTS lab head. The Associate Scientist II/Senior Associate Scientist will be responsible for routine cell line maintenance, optimization of medium to high-throughput cellular assays to quantitate mRNA or protein marker levels, and execution of siRNA efficacy screens to support preclinical drug development for multiple therapeutic targets. The ideal candidate will be flexible to changing priorities/timelines and have strong attention to detail, organization and communication skills. | 8/4/2023 |
| 4300 | ATUM Newark, CA Gene Synthesis Production Associate Bachelor’s degree in Biology Exp: entry-level |
ATUM is looking for a new member for our Gene Synthesis Production Group. ATUM is a leading bioengineering solutions provider, offering an integrated pipeline of solutions including gene design, gene synthesis, expression vectors, protein expression, protein engineering, cell line development, and master cell banking. Our products and services support breakthroughs across the life sciences. ATUM delivers DNA, proteins and cells that transform biology from a discovery science to an engineering discipline, improving the way people research, create, and live. This entry-level position is within our Gene Synthesis production group. The work includes following standard operating procedures, using automated liquid handling equipment, interfacing with our in-house database, providing support in various lab functions, and interacting with our bioinformatics department. | 8/4/2023 |
| 4301 | August Bioservices Nashville, TN Formulation & Component Prep 2nd Shift BS or BA or equivalent in a biological, chemical science, engineering, or degree in another discipline. Exp: One year |
August Bioservices is hiring Filling/Manufacturing Associates at various position levels to work in the new aseptic manufacturing facility located in Nashville, TN. The Manufacturing Technician II – Component Preparation and Formulation will operate a variety of processing and packaging equipment to prepare components for aseptic filling to include bulk formulation of aqueous and non-aqueous based products, order and receive components, dispense and formulate raw materials, manage sterilized components, operate various equipment used in the formulation process, and perform cleaning operations for process equipment and the GMP ISO 8 areas. | 8/4/2023 |
| 4302 | August Bioservices Nashville, TN Manufacturing Technician II – Filling, Lyophilization, & Terminal Sterilization 2nd Shift BS or BA or equivalent in a biological, chemical science, engineering, or degree in another discipline. Exp: One year or more |
August Bioservices is hiring Filling/Manufacturing Associates at various position levels to work in the new aseptic manufacturing facility located in Nashville, TN. The Manufacturing Technician II – Filling, Lyophilization, and Terminal Sterilization will use proper aseptic technique while performing tasks in aseptic manufacturing areas to include syringe and vial filling operations with an automated line in an RABS environment as well as routine and non-routine aseptic interventions through RABS glove ports. The technician II level will operate filling and auto loading equipment, and freeze dryers using automated control systems. The Technician II will be responsible for unloading of autoclaves, performing cleaning operations for process equipment and the GMP ISO 8 areas, management of sterilized components, and coordinating with maintenance as needed | 8/4/2023 |
| 4303 | August Bioservices Nashville, TN Microbiologist I B.A./ B.S in Biology (or related) Exp: 0–2 years |
August Bioservices is looking for a Quality Control team member that is passionate and driven professionally. August Bioservices desires a team member eager to work in an environment where people are motivated to do their best for the company and its clients. Reporting to the Manager, Microbiology, the Microbiologist I will be responsible for performing biological assays of raw materials, in-process samples, finished product, and environmental monitoring samples. He/she will work with microbiology personnel to assure test results, procedures, and methods are written, maintained, executed, and approved in accordance with approved SOPs and regulatory requirements. | 8/4/2023 |
| 4304 | Avalign Technologies Fort Wayne, IN Product Engineer Bachelor's Degree or equivalent experience required. Exp: 1+ years |
We are searching for a Product Engineer to join our team that will be responsible for the following: develop, establish and maintains engineering methods and systems to meet site specific, customer and regulatory requirements. Actively communicate initiatives to support departmental, plant and corporate operational goals. Serve as an engineering representative to provide support and guidance for new product transfers through volume production internally, at suppliers, and at customer locations. Drive new product introductions to meet customer specifications and delivery expectations. | 8/4/2023 |
| 4305 | Avantor Sciences Carpinteria, CA Process Engineer I Process Engineer I bachelor’s degree in chemical engineering Exp: 1-2 years |
Avantor is seeking an R&D Process Engineer who will be responsible for new product development of fabricated parts, process improvement projects, and capital projects ensuring the successful conclusion of all phases within an appropriate time and at appropriate cost. This role will be a full-time position based out of our Carpinteria, CA office. You will have the opportunity to implement process improvements to meet quality standards, perform feasibility studies, and solve problems. This position is involved in implementing step-change process improvements. | 8/4/2023 |
| 4306 | Avantor Sciences Bakersfield, CA R&D Chemist R&D Chemist Bachelor's degree in chemistry or biochemistry required. Exp: 1 to 3 years |
Avantor is seeking an Entry-mid level R&D Chemist to research product formulations and properties of raw materials. This person will also prepare and provide samples for laboratory and field testing for efficacy and safety and establish product specifications and procedures for R & D projects. This role will be a full-time position based out of our Bakersfield, CA office. You will have the opportunity to develop reports and documents detailing project processes, results and conclusions, and conduct research and field evaluations on new products! | 8/4/2023 |
| 4307 | Avantor Sciences Bakersfield, CA Quality Control Technician - Testing (3rd Shift) Quality Control Technician - Testing (3rd Shift) BA/BS in chemistry or science-related field preferred. Exp: 1-2 years |
Avantor is looking for a dedicated and experienced Quality Control Technician 3rd Shift. Working in partnership with under close supervision, responsible for completing product quality checks. Conducts routine testing and analysis of production work. Quality checks are typically reviewed for accuracy. Documents quality control issues as needed. This role will be a full-time position base out of Bakersfield, CA. 3rd Shift 10:00PM – 6:30AM | 8/4/2023 |
| 4308 | Avantor Sciences Irving, TX QC Lab Analyst QC Lab Analyst Bachelors of Science in Chemistry or related field. Exp: 1-2 years |
Avantor is looking for a dedicated and proactive QC Lab Analyst to optimize our NuSil team, delivering results against some of the most complex business and technology initiatives. This role will be a full-time position based out of our Irving, TX facility. You will have the opportunity to inspect and process raw materials before releasing finished products. If you have experience in quality control and are eager to grow your career - let's talk! | 8/4/2023 |
| 4309 | Avantor Sciences Saint Louis, MO Quality Control Laboratory Technician Quality Control Laboratory Technician Bachelor’s degree in a science discipline such as Chemistry, Biology, Microbiology Exp: 1+ years |
Avantor, a Global Fortune 500 company, is looking for a dedicated Quality Control Laboratory Technician to optimize our Quality Control organization. This on-site/ Saint Louis, MO role is full-time. If you have laboratory experience – let’s talk! | 8/4/2023 |
| 4310 | Aviva Systems Biology San Diego, CA Research Associate I/II – Molecular Biology B.S. or M.S. in life science or related subject. Exp: 1+ year |
Job Responsibilities Perform routine biochemistry and molecular biology techniques such as cloning, RNA/DNA isolation, cell culture, and protein purification Perform small-scale bacterial, fungal, and mammalian cell culture using aseptic techniques Operate incubator/shakers, centrifuges, and other laboratory equipment used in protein production Use electrophoresis and chromatography systems for biomolecule analysis or purification Prepare chemical solutions required for production processes Analyze Sanger sequence data for validation of expression constructs | 8/4/2023 |
| 4311 | Avomeen Ann Arbor, MI Chemist II Masters in Chemistry or Pharmacy Exp: 0-3 years |
Element has an opportunity for a Chemist II to join our growing team in Ann Arbor, MI. The Chemist II supports development of analytical methods, perform testing using a variety of technologies and draw conclusions based upon analytical data. Supports validation studies or complex sample analysis with guidance of senior staff members. Gains exposure to some of the complex tasks within the job function with moderate supervision. | 8/4/2023 |
| 4312 | AxoGen Dayton, OH Quality Analyst - 2nd Shift Bachelor’s Degree in an Engineering, Life Science discipline and/or in a related field. Exp: 0-2 years |
Axogen is hiring for a 2nd shift Quality Analyst in Dayton, OH! Job Summary of the Quality Analyst The Quality Analyst is responsible for providing quality on the floor oversight to first, second, or third shift. In this role, they will be responsible for printing batch record and other forms as needed, providing quality oversight and training to operators, performing on the floor review, performing quality control (QC) inspection and disposition of materials and products according to specifications, and performing final batch record review and product release activities. | 8/4/2023 |
| 4313 | Bausch & Lomb Rochester, NY Chemist I BS in Chemistry, or related field. Exp: 1-3 years |
The Scientist I - Chemistry is a member of a lab-based team in the Quality organization responsible for monitoring product quality by performing tests to support marketed and pre-marketed product formulations in accordance with SOPs and regulations. | 8/4/2023 |
| 4314 | BGI San Jose, CA LC/MS Research Associate – Small Molecule B.S. degree with biochemistry/chemistry major or related field. Exp: 0-2 years |
San Jose Mass Spec Lab of BGI Americas is seeking an exceptional and motivated research associate with competitive compensation. The main responsibility of this position includes, but not limited, to support the SJMS production team 1) to turn around routine customer and research projects, 2) to maintenance and operate LC-MS instrument, 3) to assist lab manager to build up metabolomics and lipidomics capability in SJMS lab, 4) to support other departments when needed. A candidate with metabolomics/lipidomics LC-MS experience is a plus; a candidate with small molecule sample prep experience is a plus. An ideal candidate will need to demonstrate that they are capable of consistently following Standard Operational Procedures (SOPs) to consistently perform sample preparation procedures for metabolomic or lipidomics analysis. A candidate with hands-on experience in HPLC, Orbitrap mass spec and working with biofluids is a plus. | 8/4/2023 |
| 4315 | BGI San Jose, CA LC/MS Research Associate – Proteomics B.S. degree with biochemistry/chemistry major or related field. Exp: 0-2 years |
BGI Americas San Jose Mass Spec (SJMS) center is seeking an exceptional and motivated research associate to join our Proteomics department at our San Jose facility. The main responsibility of this position includes, but not limited, to support the SJMS production team 1) to turn around routine customer and research projects, 2) to maintenance and operate LC-MS instrument, 3) to assist lab manager to build up additional proteomics capability in SJMS lab, 4) to support other departments when needed. An ideal candidate will need to demonstrate that they are capable of consistently following Standard Operational Procedures (SOPs) to consistently perform sample preparation procedures for proteomics and biologics characterization analysis. A candidate with hands-on experience in HPLC, Orbitrap mass spec and, working with biofluids is a plus. | 8/4/2023 |
| 4316 | Bioagilytix Durham, NC Analyst - ADA/PK - 1 Bachelor's degree in molecular biology, biochemistry, immunology, biotechnology, or related field. Exp: one (1) year |
Essential Responsibilities: Run assays independently Adhere to provided method/directive Prepare buffers Use LIMS system Participate in sample analysis Pipetting Adhere to safety requirements Keep accurate inventory of supplies for assays Responsible for accurate record keeping with regard to sponsor's samples, data, and reports (documentation according to GxP guidelines) | 8/4/2023 |
| 4317 | Bioagilytix Durham, NC Analyst - ADA/PK - 3 (JC) Bachelor's degree in molecular biology, biochemistry, immunology, biotechnology, or related field. Exp: one (1) year |
Essential Responsibilities: Run assays independently Adhere to provided method/directive Prepare buffers Use LIMS system Participate in sample analysis Pipetting Adhere to safety requirements Keep accurate inventory of supplies for assays Responsible for accurate record keeping with regard to sponsor's samples, data, and reports (documentation according to GxP guidelines) | 8/4/2023 |
| 4318 | Bioagilytix Boston, MA Analyst - ADA/PK -1 Bachelor's degree in molecular biology, biochemistry, immunology, biotechnology, or related field. Exp: one (1) year |
In this role, you will perform validation studies through the analysis of biological samples. Our clients trust us to deliver excellence in data and bioanalysis, and this role is a bedrock within our project lifecycle. You will work on a wide variety of sample validations, including biologics, protein, peptides, small molecules, and/or biomarkers with a team of expert scientists. This role is also exposed to a range of analytical instrumentation and each project looks different than the previous one. At BioAgilytix, we don’t limit you to only extracting samples - we train you to become a scientist. We are looking for candidates who have scientific lab experience in a deadline-driven setting. The best candidates are people who have hands-on experience in a lab environment (academic or professional) and are curious about applying different scientific methods, equipment and extraction processes. If you are a person who is energized by project variety and learning from top scientists in our industry, then you’ll be right at home here at BioAgilytix. | 8/4/2023 |
| 4319 | AbbVie South San Francisco, CA Associate Scientist, Conjugation Chemistry B.S. degree or M.S. degree with experience in Analytical chemistry, Biochemistry, Chemistry or other relevant discipline. Exp: 0-3+ years |
AbbVie has an opening for an Associate Scientist in Discovery Research to conduct pre-clinical research and development in the area of antibody drug conjugates (ADCs). Key Responsibilities Include: Synthesis, purification and characterization of ADCs on mg to gram scale under minimal supervision. Optimization and validation of conjugation protocols and formulation buffers. Optimization of automated techniques for ADC synthesis and purification. | 7/25/2023 |
| 4320 | AbbVie Irvine, CA Associate Scientist II/Scientist I, in vivo MS or equivalent education in pharmacology, immunology, neurobiology. Exp: 0-2+ years |
The AbbVie Ocular Discovery Research group is seeking an experienced in vivo scientist to make substantial contributions to glaucoma disease research and discovery efforts developing therapies for optic neuropathy. S/he/they will execute, develop, and communicate in vivo experiments for target identification/validation and discovery of novel therapeutics using a variety of ocular disease based in vivo rodent models. The successful candidate will leverage in vivo rodent model experience to find answers to scientific questions and move projects forward. They should be a highly motivated, hands-on scientist who is also capable of executing on scientific projects. Emphasis is on the ability to successfully perform hands-on work, demonstrate scientific skills and communicate results. Prior experience in the fields of neuroscience, ophthalmology, retinal degeneration, or vision research is preferred, but not required. In addition, the candidate should be able to manage multiple projects simultaneously and work successfully in a cross-functional and highly collaborative team environment. | 7/25/2023 |
| 4321 | AbbVie Cincinnati, OH Technician, Manufacturing II Bachelor's Degree in Engineering Exp: 0+ year |
Shipping finished materials. Maintaining inventory levels. Sampling of in process and raw materials. Running glass washer / autoclave. Buffer / media preparation. Equipment preparation (CIP / SIP). Cell culture (from vial thaw to production scale). Column chromatography. Tangential flow filtration. | 7/25/2023 |
| 4322 | AbbVie Worcester, MA Manufacturing Technician, Wed - Sat, 1st shift BS in science Exp: 1+ years |
Shipping finished materials. Maintaining inventory levels. Sampling of in process and raw materials. Running glass washer / autoclave. Buffer / media preparation. Equipment preparation (CIP / SIP). Cell culture (from vial thaw to production scale). Column chromatography. Tangential flow filtration. | 7/26/2023 |
| 4323 | AbbVie Worcester, MA Manufacturing Technician, Wed - Sat, 2nd shift Bachelor's Degree in Engineering Exp: 0+ year |
Shipping finished materials. Maintaining inventory levels. Sampling of in process and raw materials. Running glass washer / autoclave. Buffer / media preparation. Equipment preparation (CIP / SIP). Cell culture (from vial thaw to production scale). Column chromatography. Tangential flow filtration. | 7/26/2023 |
| 4324 | AbbVie Worcester, MA Manufacturing Technician, Sun - Wed, 2nd shift Bachelor's Degree in Engineering Exp: 0+ year |
Shipping finished materials. Maintaining inventory levels. Sampling of in process and raw materials. Running glass washer / autoclave. Buffer / media preparation. Equipment preparation (CIP / SIP). Cell culture (from vial thaw to production scale). Column chromatography. Tangential flow filtration. | 7/26/2023 |
| 4325 | AbbVie Worcester, MA Manufacturing Technician, Wed - Sat, 2nd shift Bachelor's Degree in Engineering Exp: 0+ year |
Shipping finished materials. Maintaining inventory levels. Sampling of in process and raw materials. Running glass washer / autoclave. Buffer / media preparation. Equipment preparation (CIP / SIP). Cell culture (from vial thaw to production scale). Column chromatography. Tangential flow filtration. | 7/26/2023 |
| 4326 | ABEC Bethlehem, PA Product Engineer - Process Sciences Bachelor's degree in Engineering, Life Sciences, or Sciences field (Biological, Chemical, Physics, or equivalent experience). Exp: 1 year |
The Process Sciences Engineer is responsible for collaborating, leading, and executing process sciences efforts, specifically focused on Computational Fluid Dynamics Modeling and Empirical Data Generation to support internal or/and external projects during the implementation new technology; knowledge generation or any ABEC key activity. This role involves create predictive models, conducting experiments, collecting, and analyzing data, protocol and report preparation, and customer interaction. For this role, a certain level of independency and initiative is needed. Additionally, the Process Sciences Engineer will contribute to activities such as marketing content generation, new product development support, and sales and services. | 7/26/2023 |
| 4327 | Analytical Biological Services Wilmington, DE QC Laboratory Associate BS or BA or higher in biological sciences or equivalent field. Exp: 1+ years |
The QC laboratory associate is responsible for performing quality control testing with rapid turnaround and accurate results, to ensure high quality of our cell culture products for our clients. The associate must understand the basics of molecular biology, cellular biology, and cell culture and will be responsible for job management following the completion of the production phase through the transition to shipment or storage. Successful job management will include performing tests in-house, preparing samples for outsourcing, accurate record keeping, and communication of results, knowledge, and product information to team members and clients. This position requires strong time management, attention to detail, organization, precise record keeping, and excellent communication skills. | 7/26/2023 |
| 4328 | Analytical Biological Services Wilmington, DE Cell Culture Scientist BS or BA or higher degree in biological sciences. Exp: 1+ years |
Cell Culture Scientist position is currently available in Wilmington, DE. ABS Inc. (www.absbio.com) is a successful bioscience company with over 29 years’ experience providing cell culture and other services for R&D to pharmaceutical and biotechnology clients worldwide. | 7/26/2023 |
| 4329 | Analytical Biological Services Wilmington, DE Biorepository Technologist I (In-Sourced) Bachelor’s Degree in a medical or biological science preferred. Exp: 1+ years |
Primary duties and responsibilities of the Biorepository Technologist I (In-Sourced) included but are not limited to: -Receive biospecimens including frozen, fixed, or fresh solid and liquid samples -Coordinate with shipping and receiving department to ensure all shipments are appropriately tracked -Coordinate with internal clinical study team to ensure sample and data accuracy -Communicates by written and verbal methods with related departments to assure samples arrive in the appropriate lab -Record sample quality concerns and provide feedback to collection site or central lab -Document sample information in laboratory database from source documents -Accession samples and appropriate data in the laboratories electronic data management system -Pull samples from inventory when requested by scientists for internal projects | 7/26/2023 |
| 4330 | Abveris Boston, MA Research Associate - Protein Analytics Bachelor’s or Master’s degree in a scientific discipline required (Biology, Biochemistry, Biochemical Engineering) Exp: 1-3 years |
We are seeking a motivated individual to join our team and expand our bioanalytical department. Using state-of-the art technologies and workflows, this Research Associate would work with the Protein Analytics team to ensure project-specific deliverables are met across a diverse panel of discovery campaigns. The role would involve wet lab experimental design, execution, and data analysis for multiple custom antibody development projects incorporating various biologics assay formats. | 7/26/2024 |
| 4331 | Abveris Boston, MA Research Associate - Molecular Biology Degree in Biology or other related discipline Exp: 1+ years |
We are seeking a motivated individual to join our Molecular Biology team and contribute to cloning, antibody sequencing, single B cell discovery and additional molecular biology workflows. The role will be lab-based and integral to expanding our molecular biology capabilities as our company continues its rapid growth trajectory and passion for integrating state-of-the-art technology and custom antibody discovery techniques. The ideal candidate will have previous hands-on experience with immune cell sample processing, PCR amplification and cloning techniques. Technical proficiency in a combination of the following is also desired: Next Generation Sequencing (NGS) workflows, antibody sequence analysis and high throughput downstream molecular biology techniques required for various cloning methods and subsequent recombinant expression. Meticulous attention to detail, proficient reasoning and problem-solving skills are cornerstones for a successful candidate. | 7/26/2023 |
| 4332 | Associates of Cape Cod East Falmouth, MA Quality Control Analyst I B.S. degree in a relevant scientific discipline Exp: 0-2+ years |
In this role you will perform chemical and/or biological assays of commercial product raw materials, production intermediate and bulk samples, finished product, environmental monitoring samples, process and cleaning validation samples. Assays are qualitative, quantitative and investigational in nature and are performed in compliance with cGMP, ACC SOPs, and FDA Analyst has working knowledge of relevant QC techniques, policies and procedures to perform QC tasks and document results. Analyst receives minimal supervision on routine assignments and detailed instructions on new assignments. | 7/26/2023 |
| 4333 | Acumed Addison, TX Quality Engineer 1 Bachelor’s degree in an engineering or science discipline. Exp: 0-3 years |
The Quality Engineer 1 is responsible for supporting all quality activities related to the production and inspection of sustaining products. The QE 1 drives Quality objectives in all sustaining activities, ensuring product and process conformance to global standards (including FDA AND ISO 13485). The purpose of this position is to serve as a Quality leader during manufacturing to ensure high product quality, reliability, and process capability and facilitate teams in identifying, documenting, assessing, correcting, and presenting quality issues using risk analysis and root cause analysis tools. | 7/26/2023 |
| 4334 | ADMA Biologics Boca Raton, FL Raw Material Specialist I B.S. or associate degree in Chemistry, Biochemistry, Biology or related science discipline. Exp: 0-3 years |
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Raw Material Specialist I! The Raw Material Specialist I will perform quality control raw material processing and testing. Following general instructions on routine work and detailed instructions on new assignments. | 7/26/2023 |
| 4335 | ADMA Biologics Boca Raton, FL Technician I Fill Finish Operations - Night Shift Bachelor’s degree or equivalent experience Exp: Entry-Level |
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Technician I Fill Finish Operations - Night Shift in Boca Raton, FL! The Technician I Fill Finish Operations - Night Shift position is responsible for the final finishing of plasma products. This includes aseptic filling, visual inspection, vial labeling, and final serialization and packaging. This position is under oversight of the Group Leader and reports to the Supervisor/ Sr. Manager Fill Finish Operations. | 7/28/2023 |
| 4336 | ADMA Biologics Boca Raton, FL Technician I Fill Finish Operations - Day Shift Bachelor’s degree or equivalent experience Exp: Entry-Level |
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Technician I Fill Finish Operations - Day Shift in Boca Raton, FL! The Technician I Fill Finish Operations - Day Shift position is responsible for the final finishing of plasma products. This includes aseptic filling, visual inspection, vial labeling, and final serialization and packaging. This position is under oversight of the Group Leader and reports to the Supervisor/ Sr. Manager Fill Finish Operations. | 7/28/2023 |
| 4337 | Admera Health South Plainfield, NJ Associate Scientist I/II Bachelor’s degree in Biological Sciences or M.S. in Biological Sciences. Exp: BS: 1-3 years; MS: 1 year |
Admera Health is looking for an Associate Scientist I/II to join our growing team! | 7/28/2023 |
| 4338 | Akoya Biosciences Marlborough, MA Research Associate II (Tuesday through Saturday shift) AS or BS Degree in Life Sciences. Exp: One (1) to five (5) years |
Please note: The position is a full-time, on-site role working in the Akoya Advanced Biopharma Solutions (ABS) laboratory located at Marlborough, MA and the work schedule is Tuesday through Saturday. Position Summary/Impact: We are seeking for a highly motivated Research Associate II to join the Akoya Advanced Biopharma Solutions (ABS) group located in Marlborough, MA. The successful candidate will work in a team-oriented environment providing clients with multiplexing immunofluorescence staining. The candidate will have worked in a clinical or preclinical pathology laboratory with experience in high-throughput histology with focus on immunohistochemistry. The candidate will work with lab personnel on reagent preparation, troubleshooting and running qualification studies. Knowledge of antibody validation methods, immunofluorescence (IF) and quantitative pathology approaches are a plus but not required. The successful candidate must have experience in basic image analysis and be part of a team that provides imaging for clients. They should also be familiar with LIMS systems and have experience working in a regulated laboratory setting such as a CAP/CLIA and GCLP. | 7/28/2023 |
| 4339 | Alcami Wilmington, NC Associate Scientist I/II Bachelor’s degree in Chemistry or related field. Exp: 0 – 4+ years |
The Associate Scientist I or II is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of active pharmaceutical ingredients development or pharmaceutical manufacturing. This position may also be required to work on method development/method validation projects. Typical types of testing include: assays (potencies, related substances, residual solvents, metals etc.), moisture content, identification, and various other wet chemistry based measurements. HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations, UV, DSC, TGA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client/vendor supplied or developed by Alcami). The Associate Scientist II must have the ability to efficiently organize the routine work with minimum supervision and to properly evaluate and interpret generated data is required. The Associate Scientist II will occasionally be called upon to support and mentor other Analytical Chemists within the lab. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 7/28/2023 |
| 4340 | Alcami Wilmington, NC Associate Scientist I/II -Microbiology Bachelor’s degree in Chemistry, Biology, Microbiology or a related field with course work in Microbiology. Exp: 0 – 4 + years |
The Associate Scientist I or II is accountable for driving results in a fast-paced environment by performing microbiological routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing and stability. Bacterial endotoxins, sterility, microbial examination and antimicrobial effectiveness based methodologies are commonly employed in the described testing. Other key methodologies applied include: liquid particulate matter and genetic identification testing. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client/vendor supplied or developed by The Company). The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 7/28/2023 |
| 4341 | Alcami Charleston, SC Associate Scientist I/II Microbiology 2nd Shift Bachelor’s degree in Chemistry, Biology, Microbiology or a related field with course work in Microbiology. Exp: Level I: 0 – 2 + years |
The Associate Scientist is accountable for driving results in a fast-paced environment. Level I is responsible for performing and documenting the monitoring of the pharmaceutical manufacturing environment and utilities in compliance with cGMP and internal SOPs. The incumbent will provide support to manufacturing and laboratory operations. Level II is responsible for performing complex microbial analysis and assisting with method development and validation. The position plays an important role in environmental monitoring through accurate sampling and leadership of junior employees. The Associate Scientist II may assist in GMP review, provide problem solving support and Laboratory Investigation Report ownership for the Microbiology Department. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 7/28/2023 |
| 4342 | Alcami Morrisville, NC Associate Scientist II - Raw Materials Bachelor's degree in Pharmaceutical Sciences or Chemistry or Master's degree. Exp: BS: 1 years; MS: 0 years |
The position is responsible for support of compendial testing group and manages priorities of this team to provide the timely, compliant and accurate testing of raw materials, critical utilities, in-process samples and finished product. This position will collaborate with cross-functional teams and will work side-by-side with other scientists and professionals to drive the scientific agenda. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 7/28/2023 |
| 4343 | Aldevron SE Bothell, WA Oligonucleotide Manufacturing Chemist BS in Chemistry, Biochemistry preferred. Exp: 0-2 years |
The Oligonucleotide Manufacturing Chemist supports manufacturing of synthetic oligonucleotides under a cGMP environment for use in Cepheid in-vitro diagnostic products. The Chemist will use scientific knowledge and understanding to execute and document standard operating procedures to ensure successful manufacturing and on time delivery of Oligonucleotides. They will contribute to the successful transfer of new products from development to manufacturing ensuring robust manufacturing processes at commercialization and support processes to ensure performance within expected parameters. This position is part of the Oligonucleotide Manufacturing team and will be located onsite in Bothell, Washington facilities. | 7/28/2023 |
| 4344 | Aldevron SE Bothell, WA Manufacturing Chemist Master’s degree in Chemistry, Biochemistry, Chemical Engineering or a related field. Exp: 0+ years |
The Manufacturing Chemist is responsible for performing tasks associated with the production of oligonucleotides in a dynamic fast paced GMP manufacturing environment. The position will also work closely with development and Quality teams to transfer and qualify new technology and processes from development into manufacturing. This position is part of the Oligonucleotide Manufacturing team and will be located onsite in Bothell, Washington facilities. At Cepheid, our vision is to be the leading provider of seamlessly connected diagnostic solutions. | 7/28/2023 |
| 4345 | Aldevron Miami, FL Manufacturing/Process Engineer II Master’s degree. Engineering degrees in mechanical, electrical, and industrial preferred. Exp: 0+ years |
The Manufacturing/Process Engineer II for Beckman Coulter Diagnostics is responsible for providing day to day technical support and driving complex root cause investigations, for the instrument manufacturing product lines, including the assembly and final test processes, to drive quality and on-time delivery for our customers. This position is part of the Manufacturing Operation located in Miami, Florida and will be on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Manufacturing Engineering Team and report to the Manufacturing Engineering Manager responsible for providing technical support to the manufacturing lines of Beckman Coulter’s premier Diagnostics products. | 7/28/2023 |
| 4346 | Aldevron Madison, WI Associate Scientist II, Upstream Biomanufacturing (Fermentation) B.S. degree Exp: 0-2 or more years’ |
The Associate Scientist II position is part of the Upstream Biomanufacturing department located in Madison, WI and will be onsite. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Upstream Biomanufacturing team and report to the Manager of Upstream Biomanufacturing and will be responsible for supporting the execution of 1-L to 1000-L scale microbial fermentations. This role works collaboratively with team members and as an individual contributor. This position requires excellent laboratory skills, attention to detail and excellent documentation practices. | 7/28/2023 |
| 4347 | Aldevron Boston, MA Lab Scientist, Spatial Biology BS is the minimum educational requirement (preferably in the biological sciences). MS in biological sciences is strongly preferred. Exp: 1+ years |
Come join the spatial biology team at Leica Microsystems. We are a rapidly growing group in an exciting scientific space, and we come to work every day knowing we can make a difference in human health. In your role as Lab Scientist, you will carry out projects based on multiplexed imaging, including tissue/cell prep, imaging and analysis. Be prepared to use your creativity and problem solving skills to help the team develop new solutions. Ensures laboratory environment and practices comply with guidelines set forth by company and regulatory agencies This role is hybrid and based out of our new Waltham, Massachusetts location . | 7/28/2023 |
| 4348 | Aldevron Madison, WI Associate Scientist II - Upstream PD Bachelor’s degree in biology, biotechnology, molecular biology, biochemistry, chemistry, or a closely related field. Exp: 0-2 years |
This position is part of the Upstream Process Development Team located in Madison and will be on-site. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Upstream Process Development Team and report to the Manager responsible for assisting on protein expression projects and media preparation. | 7/28/2023 |
| 4349 | Alliance Pharma Malvern, PA Assistant Scientist I BA/BS or higher; all experiences will be evaluated. Exp: 1+ years |
Responsibilities: · Prepare reagents, standards, and control samples · Analyze samples using various techniques specific to department · Operate analytical equipment · Maintain analytical equipment · Ensure lab area is clean and inspection ready at all times · Remove lab waste · Record tasks in accordance with Good Documentation Practices (GDP) · Learn and apply regulatory requirements; GLP, GCP, 21CFR Part 11 · Follow applicable SOPs and procedural documents · Learn how to review and evaluate data results · Other tasks as assigned | 7/28/2023 |
| 4350 | Alliance Pharma Malvern, PA Assistant Scientist II - Immunoassay BA/BS or higher. Exp: 1-2 years |
Responsibilities: • Prepare reagents, standards, and control samples • Analyze samples using various techniques specific to department • Perform method validation or qualification • Operate analytical equipment • Maintain analytical equipment • Ensure lab area is clean and inspection ready at all times • Remove lab waste • Record tasks in accordance with Good Documentation Practices (GDP) • Understand and apply regulatory requirements; GLP, GCP, 21CFR Part 11 • Follow applicable SOPs and procedural documents • Review and evaluate data results • Other tasks as assigned | 7/28/2023 |
| 4351 | Alliance Pharma Malvern, PA Assistant Scientist II - LCMS BA/BS or higher. Exp: 1-2 years |
Responsibilities: • Prepare reagents, standards, and control samples • Analyze samples using various techniques specific to department • Perform method validation or qualification • Operate analytical equipment • Maintain analytical equipment • Ensure lab area is clean and inspection ready at all times • Remove lab waste • Record tasks in accordance with Good Documentation Practices (GDP) • Understand and apply regulatory requirements; GLP, GCP, 21CFR Part 11 • Follow applicable SOPs and procedural documents • Review and evaluate data results • Other tasks as assigned | 7/28/2023 |
| 4352 | Allogene Therapeutics Newark, CA Associate, Cell Therapy Manufacturing (Contract) Bachelors or Associates in relevant science or engineering discipline. Exp: 0-2 years |
We are seeking a highly motivated Associate, Cell Therapy Manufacturing to join our Manufacturing team. This is a 6+ month contract role that could be extended before a decision on the full-time role is made. This role will work within the Manufacturing team in supporting our efforts in an exciting new area of cancer immunotherapy. This position is based out of Newark, CA. The position will report to the Senior Manager, Manufacturing and will support the successful tech transfer and operational readiness process, using knowledge of cGMP regulations to ensure manufacturing readiness. Responsibilities of primary importance are: to ensure the successful, time-sensitive GMP manufacture and release of cell therapy products; to follow all processes and procedures related to operations in full compliance with cGMP, CFRs, site quality systems and company policies; and to promote a culture of quality and compliance. The successful candidate will have experience in a regulated biotech or pharmaceutical setting and will have proven competency and expertise in the GMP manufacture of cell-based therapies. | 7/28/2023 |
| 4353 | Allogene Therapeutics South San Francisco, CA Associate Scientist, Analytical Development (Contract) Masters, or bachelors. Exp: 1-2 years |
We are seeking a highly motivated Associate Scientist to join our Analytical Development group and contribute to the commercialization of allogenic CAR T therapies. (S)he will play a key role in CAR T cell therapy related analytical assay development and execution of drug product release and stability assay. The individual will work closely with peers in assay development, assay qualification, execution of the release and characterization assays, comprehensive risk assessments, and data synthesis that allows for the subsequent analytical assay tech transfer. This role will be based at the headquarters in South San Francisco, CA. | 7/28/2023 |
| 4354 | Allogene Therapeutics South San Francisco, CA Associate Scientist (Contract) BSc or Msc degree. Exp: 1+ year |
Allogene is seeking a highly determined, results-oriented, self-starter who demonstrates personal accountability for outcomes and is motivated by increasing levels of responsibility, to join a dynamic team responsible for successful development and characterization of clinical-scale manufacturing of Allogeneic Chimeric Antigen Receptor T-cell therapies (Allo CAR T™). The successful candidate will help to support appropriate flow cytometry-based analytical methods for the characterization, release and stability testing of CAR T products. This position will also contribute to the development of novel technologies and approaches to meet future CAR T analytical needs and work in close collaboration with key stakeholders, including the CAR T Research and Process Development groups. This is a 1-year contract position in South San Francisco, CA. | 7/28/2023 |
| 4355 | Alnylam Pharmaceuticals Cambridge, MA Associate Scientist II, RNAi Discovery BS Chemistry, Biochemistry or related discipline. Exp: 0-2 years |
The RNA Synthesis team is seeking a motivated individual to join our Annealing group as an Associate Scientist II. The Annealing group is responsible for the quality control of single stranded RNA using analytical techniques such as liquid chromatography and mass spectrometry. In addition the group is responsible for formulating high quality test articles (siRNA) to support research efforts across multiple therapeutic areas. This position is onsite and will be primarily located at our 675 W. Kendall St. location in Cambridge, MA. | 7/28/2023 |
| 4356 | ALPCO Diagnostics Salem, NH Research Associate BA/BS in the Sciences. Exp: 0-3 years |
Overview of position: A successful candidate in this position will be able to multi-task and thrive in a fast-paced work environment, participate in research and development activities, and utilize established mathematical and scientific techniques to compile and analyze data. He/She will have knowledge of commonly used laboratory concepts, practices, and procedures, while relying on instructions and pre-established guidelines to perform job functions. The position requires someone with a strong work ethic, who will operate with a constant sense of urgency and commercial purpose. He/She will write technical reports detailing procedures, outcomes, and observations, can communicate and collaborate with team members, and take on additional assignments as needed. Occasional travel to scientific congresses or training may be required. | 7/28/20234 |
| 4357 | Research Associate I Jupiter, FL Research Associate I Bachelor’s Degree or equivalent in Biology, Immunology, Biochemistry, Biotechnology preferred. Exp: 1 or more years |
Alphazyme, a Maravai LifeSciences company, is looking for a Research Associate I to join our growing team. The Research Associate I supports the Company’s enzyme development projects according to internal prioritization and undertakes a variety of laboratory procedures of technical nature. This position will timely and accurately prepare various reagents, such as media, bacterial plates, and competent cells, bacterial stock maintenance, support in any area regarding enzyme expression, as well as maintenance of clean and organized laboratory space and equipment. | 7/28/2023 |
| 4358 | Research Associate Richmond, CA Research Associate B.S. or M.S. degree in Biochemistry, Molecular Biology or related discipline. Exp: 1 year |
ALSTEM, INC is a growing research biotechnology company located in Richmond, CA. ALSTEM is a nimble provider of tools specializing in virus packaging, genome editing, cell engineering and stem cells for life science research. ALSTEM is looking for a highly organized and energetic Research Associate with a B.S or M.S. degree to join its scientific team. The candidate will be responsible to work as a team at all levels which will include but will not be limited to product testing and QC, and custom service projects following SOPs and protocols to support customer workflows. | 7/28/2023 |
| 4359 | Serotiny South San Francisco, CA Research Associate / Senior Research Associate – Cell Therapy Research Associate: BSc.; Sr. Research Associate: MSc. Exp: BSc.: 0-3 years; MSc. >2 years |
Serotiny is looking for a RA/SRA who is excited to work closely with a team of protein engineers and cell biologists to build out and deploy Serotiny's high-throughput methods to characterize and develop cutting edge therapies. The position will contribute towards the development of a novel platform to generate and characterize CAR immune cells for solid tumor indications. | 7/19/2023 |
| 4360 | SetPoint Medical Valencia, CA Quality Engineer - Temporary Position (3 - 6 months) BS in an engineering field Exp: 1+ years |
SetPoint Medical is seeking a temporary Quality Engineer to assist in the process of documenting Quality Management System (QMS) policies and procedures throughout the organization. The successful candidate must be an organized, self-motivated individual with the ability to adjust to workloads based upon the changing priorities that come with working in a fast-paced small company environment. The selected candidate will work under the Director, Quality Assurance. | 7/19/2023 |
| 4361 | Shockwave Medical Santa Clara, CA Manufacturing Engineer I Bachelor’s degree in Biomedical Engineering, Mechanical Engineering Exp: 0-3 years |
The Manufacturing Engineer I is responsible for providing engineering support to Production. The Manufacturing Engineer is also responsible for designing, developing, testing, and implementing processes, tooling, and fixtures for commercial product. In addition, the Manufacturing Engineer will work closely with the development teams developing and refining manufacturing process to ensure successful transfer into the company’s manufacturing operations. | 7/19/2023 |
| 4362 | Spark Therapeutics Philadelphia, PA Pre-Clinical Manufacturing Associate - Upstream BA/BS in biological sciences, engineering, biochemistry, or related discipline preferred Exp: 0 – 3 years |
We don’t follow footsteps. We create the path. This position is a key participant in the day-to-day operation and planning of upstream production for rAAV processes, where the production is performed with either adherent cell culture in roller bottles (up to 200 per sublot) or suspension cell culture in stirred tank bioreactors (from bench scale up to ≥ 200L). This includes production of both Research grade and GLP grade materials. Additionally, the individual will contribute to the implementation of documentation in order to support research and GLP rAAV vector manufacturing. This position requires knowledge and experience with upstream process development, including familiarity with both adherent and suspension cell culture production processes. Experience with benchtop bioreactors is a plus. Good written and verbal communication skills and ability to work effectively in a team environment are required. | 7/20/2023 |
| 4363 | Talis Biomedical Chicago, IL Senior Research Associate, Assay Development MS or equivalent in Molecular Biology, Biochemistry, Biomedical Engineering, Biochemical Engineering, Chemical Engineering, or a related field Exp: 1-5 years |
We are seeking a highly motivated, talented, and driven Senior Research Associate to join the Assay Development group in the R&D division at Talis Biomedical. This is a great opportunity to join a collaborative and dynamic team effort to enable the development of rapid point-of-care diagnostic tests. The successful candidate will work in product development, including verification and validation activities. You will author, review, and edit SOPs, study protocols, reports, and other documentation as needed. You will work collaboratively with others in Assay Development teams and other departments at Talis, including Assay Research, Operations, Quality, and Engineering. A strong understanding of nucleic acid biochemistry and experience working on cross-functional teams is highly desired. | 7/20/2023 |
| 4364 | Tevard Biosciences Cambridge, MA Research Associate, in vivo pharmacology BS/MS in Neuroscience, Physiology, Molecular/Cellular Biology, or a related Life Science discipline. Exp: 0-2 years’ |
We are looking for Research Associate (RA-I or RA-II) with an innovative mindset, great attention to detail and ability to work collaboratively to solve problems, to help advance therapeutic candidates to the clinic. The successful candidate will have an opportunity to positively impact patients with serious unmet medical needs while working closely with our world-class scientific team, including with company’s scientific co-founders. In this position, you will collaborate with the in vivo pharmacology team to study effects of therapeutic lead candidates. The RA will work with animal models for rare genetic diseases and will be responsible for executing experiments to quantify molecular, cellular, and physiological readouts, in addition to supporting in vivo dosing studies and related research activities within the in vivo pharmacology group. This is an exciting opportunity for a motivated scientist to further develop their skills in neuroscience, physiology and gene therapy while helping to make an impact on lives of patients suffering from rare diseases. | 7/20/2023 |
| 4365 | Tevard Biosciences Cambridge, MA Research Associate – tRNA and mRNA biology BS/MS in Neurobiology, Molecular/Cellular Biology, physiology, or a related discipline. Exp: 1+ years |
As an expert scientist in cellular neurobiology, you will be responsible for establishing cellular assays to demonstrate in vitro proof of concept for Tevard’s tRNA therapeutic leads and characterize the cellular activity and downstream disease-relevant biology to help prioritize candidates for in vivo studies. | 7/20/2023 |
| 4366 | Thrive Earlier Detection San Diego, CA Research Associate II Bachelor’s degree in Life Sciences, Medical Technology, Clinical Laboratory Science, Chemical/Physical/Biological Science, or related field. Exp: 1+ years |
The Research Associate II, with guidance from more experienced scientists, is responsible for the day to day experimentation and is responsible for the execution of bench experiments and analysis of data. Working in a team setting, the Research Associate II will primarily be involved in Research and Development projects assisting in translating research ideas and concepts into the product development pipeline towards development of diagnostic assay products. We are seeking a talented and highly motivated Research Associate II to join our Technology Assessment team in San Diego. The Technology Assessment group is responsible for the evaluation of novel methodologies and instrumentation to benefit Exact Sciences’ product portfolio spanning the cancer care continuum. The successful candidate will work with a small team in the evaluation of emerging technologies – including novel NGS platforms – in support of a wide variety of research and product development applications and collaborate with cross-functional teams to achieve key company objectives. This role is ideal for a driven individual with collaborative spirit and a strong background in NGS technologies and demonstrated capacity to learn quickly. | 7/21/2023 |
| 4367 | Thrive Earlier Detection Madison, WI Systems Test Engineer II/III Bachelor’s degree in engineering, computer science or related field. Exp: 1+ year |
The Systems Test Engineer II works with the Systems Development team to ensure that custom in vitro diagnostic systems meet design and customer requirements. The Systems Test Engineer II uses a technical background in software development and engineering, combined with an understanding of the system design, to analyze user needs, requirements and specifications to create testing strategies and plans for verification and validation of the system designs. | 7/21/2023 |
| 4368 | Thrive Earlier Detection Madison, WI Clinical Laboratory Science I - Contract Bachelor's degree in a chemical, physical, biological or clinical laboratory science or medical technology from an accredited institution. Exp: 1+ years |
The Clinical Laboratory Scientist I performs laboratory analysis on clinical specimens using established laboratory procedures. The Clinical Laboratory Scientist I duties will include but are not limited to; processing of specimens, performance of moderate, and highly complex analytical testing, establishing, performing and documenting quality assurance, quality control, equipment maintenance, and accurately documenting all work performed under the direction of the Laboratory Medical Director. As a Clinical Laboratory Scientist I, you will recognize and resolve problems using good laboratory practices. This role is a contract position ending in March 2024. | 7/21/2023 |
| 4369 | Thrive Earlier Detection San Diego, CA R&D Laboratory Technician I Bachelor’s or Associate degree in biotechnology or field as outlined in the essential duties. Exp: 1+ years |
The R&D Laboratory Technician I is an entry level position providing support for common R&D laboratory operations functions. The position entails following detailed instructions and established procedures with frequent supervision. Responsibilities include lab organization, general lab and equipment maintenance, consumables inventory and stocking, reagent generation, and miscellaneous initiatives to help the lab run efficiently. Additionally, this position assists with sample ordering and management of both non-infectious and potentially infectious materials. The R&D Laboratory Operations Technician I is expected to follow all laboratory and safety policies, procedures, and reporting practices. | 7/21/2023 |
| 4370 | Thrive Earlier Detection Marshfield, WI Clinical Laboratory Technician - Rare Disease Sequencing Laboratory Bachelor's degree in a chemical, physical, biological or clinical laboratory science or medical technology from an accredited institution. Exp: 1+ years |
The Clinical Laboratory Technician is responsible for performing standard laboratory procedures within the assigned department/laboratory. The Clinical Laboratory Technician will analyze data and may assist with research and development. This incumbent will be relied upon to follow laboratory protocols and maintain high quality levels. This role is located onsite in Marshfield, WI and works in our Sequencing Laboratory. The training for this role is 8 weeks Monday-Friday 8am-4:30pm. After training, the shift is a rotating 4-day/10-hour shift. Wednesday-Friday/Tuesday 7am-5:30pm with every 3rd weekend, 6:00am-4:30pm.The Clinical Laboratory Technician is responsible for performing standard laboratory procedures within the assigned department/laboratory. | 7/21/2023 |
| 4371 | Toxicon RTP, NC Technologist Trainee - Molecular Genetics B.A./B.S. in Biology, Chemistry, Medical Technology or relatable life science field. Exp: 0-1 year |
The Integrated Genetics Division is seeking a Molecular Technologist Trainee or Technologist to join their Molecular Genetics team in RTP, NC! The Molecular Genetics department at CMBP performs a wide array of testing for heritable disorders, including tests for cystic fibrosis, Tay-Sachs disease, Gaucher disease, fragile X syndrome, thalassemia, thrombophilia, and many more. Assays performed in the Molecular Genetics Department utilize a variety of scientific techniques, including PCR, fragment analysis, and gel electrophoresis. Participate in LabCorp’s in-house training program for the field of molecular genetics. Receive in-depth training to prepare for the ASCP-MB board exam and certification. Training program is a two year commitment, and requires signing a training reimbursement agreement. The schedule for this position will be: Tuesday – Saturday, 7am-3:30pm.The Integrated Genetics Division is seeking a Molecular Technologist Trainee or Technologist to join their Molecular Genetics team in RTP, NC! | 7/21/2023 |
| 4372 | Toxicon RTP, NC Technologist Trainee - Molecular Genetics B.A./B.S. in Biology, Chemistry, Medical Technology or relatable life science field. Exp: 0-1 year |
The Integrated Genetics Division is seeking a Molecular Technologist Trainee or Technologist to join their Molecular Genetics team in RTP, NC! The Molecular Genetics department at CMBP performs a wide array of testing for heritable disorders, including tests for cystic fibrosis, Tay-Sachs disease, Gaucher disease, fragile X syndrome, thalassemia, thrombophilia, and many more. Assays performed in the Molecular Genetics Department utilize a variety of scientific techniques, including PCR, fragment analysis, and gel electrophoresis. Participate in LabCorp’s in-house training program for the field of molecular genetics. Receive in-depth training to prepare for the ASCP-MB board exam and certification. Training program is a two year commitment, and requires signing a training reimbursement agreement. The schedule for this position will be: Sunday - Thursday, 7am-3:30pm | 7/21/2023 |
| 4373 | Toxicon RTP, NC Cytogenetics Technologist Trainee - 2nd Shift B.A./B.S. in Biology, Chemistry, Medical Technology or related life science. Exp: 0 year |
LabCorp and the Integrated Genetics Division is seeking a Cytogenetics Technologist Trainee to join their Cytogenetics team in Microarray, located in RTP, NC! Assays performed in the Cytogenetics Department utilize a variety of scientific techniques, including prenatal culturing, DNA extraction, real-time PCR, PCR, SNP microarray, and gel electrophoresis. Participate in LabCorp's in-house training program for the field of Cytogenetics. Receive in depth training and preparation for the ASCP board examination and ASCP-CG or ASCP-MB certification | 7/21/2023 |
| 4374 | Toxicon RTP, NC Cytogenetic Technologist Trainee - 2nd Shift Bachelors in Biology, Chemistry, or relatable life science field. Exp: 0+ years |
The Integrated Genetics Division is seeking a Cytogenetics Technologist Trainee to join their Cytogenetics team! Assays performed in the Cytogenetics Department utilize a variety of scientific techniques, including specimen culturing, slide preparation, and chromosome analysis. Participate in LabCorp's in-house training program for the field of Cytogenetics. Receive in depth training and preparation for the ASCP board examination and ASCP-CG certification. Training program is a two year commitment and requires signing a training reimbursement agreement. The schedule for this position will be Sunday - Thursday 1:00pm-9:30pm. | 7/21/2023 |
| 4375 | Toxicon Durham, NC Flow Cytometry Analyst Bachelors in Medical Technology or Bachelors in chemical, physical or biological science. Candidate must possess or be eligible for ASCP certification Exp: 0 - 6 months |
***** $5,000 Sign-On Bonus Offered for External Candidates ***** Integrated Oncology, a LabCorp Specialty Testing Group, provides reference anatomic pathology, hematopathology and molecular pathology testing services to hospitals, health systems and independent oncology practices. Integrated Oncology is focused on providing world class solutions to better the lives of patients living with cancer. We are offering exciting opportunities to join our team as a Flow Cytometry Analyst - Technologist in Research Triangle Park at the Center for Molecular Biology and Pathology, Durham, NC. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". This Analyst will work alongside a highly trained staff with the latest technology. Our services are performed with the utmost care, expertise, integrity and respect for the patient. The work schedule for this position will be Wednesday-Saturday 10:00am-8:30pm, 1st shift | 7/21/2023 |
| 4376 | Toxicon Burlington, NC Technologist Trainee Bachelor's degree in Biology, Chemistry, Medical Technology or a related science, as required by CLIA. Exp: 0+ years |
$1,000 Sign-On Bonus for External Candidates Only! Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist Trainee in Burlington, NC. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". The schedule for this position will be: 2nd shift, Tuesday-Friday, 2:00pm-12:30pm. Eligible for 10% shift differential due to 2nd shift hours | 7/21/2023 |
| 4377 | Toxicon Burlington, NC Technologist Trainee for Toxicology Bachelor's degree in Biology, Chemistry, Medical Technology or a related science. Exp: 0+ years |
$1,000 Sign-On Bonus for External Candidates Only! Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist Trainee in Burlington, NC. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". The schedule for this position will be: 1st shift, Monday-Friday, 8:00am-4:30pm. | 7/21/2023 |
| 4378 | Trevigen Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
This position is responsible for the developing and or formulation of standards, controls, calibrators, and intermediates in the production and development of Bio-Techne's Luminex, Q-kit, DuoSet, and Simple Plex product lines. Day to day responsibilities involve hands on work in a production laboratory running assays for ELISA and Luminex. You will draft and revise standard operating procedures, manage a production schedule, and analyze assay data to further the ongoing development of new and existing products within Bio-Techne’s evolving portfolio. | 7/21/2023 |
| 4379 | Trevigen Minneapolis, MN Research Associate, Antibody Applications B.S. degree in Biochemistry, Chemistry, Biology, or a related field. Exp: 0 - 2 years |
The Research Associate is responsible for routine quality control testing of antibodies using immunohistochemistry (IHC) and immunocytochemistery (ICC). The testing includes culturing and handling of stem cells, primary cells, and basic cell lines for the use in ICC. The handling of fixed tissues for use in IHC. The position requires routine documentation, data analysis and good communication of results. | 7/21/2023 |
| 4380 | Trevigen Minneapolis, MN Research Associate, Analytical QC B.S. degree in Biochemistry, Chemistry, Biology, or a related field. Exp: 0 - 2 years |
As the Research Associate, Analytical Quality Control Analyst you will perform routine quality control testing of protein, peptide or antibody products using standard operating procedures to determine lot status, product release and product stability. Tests include concentration determination, SDS-PAGE with densitometry, endotoxin assay, PCR, HABA, conductivity, total organic carbon and other testing as assigned. Participation in the validation of new and existing laboratory methods is also expected. The position requires routine documentation, analysis, and communication of results within the department and across different groups. Other duties include instrument calibration and maintenance, record keeping, and lab support. Within this job function, the Research Associate must also pursue annual goals that aim to facilitate innovation, efficiency, productivity, and team building across the QC Department or the entire company. Perform additional duties as assigned | 7/21/2023 |
| 4381 | Trevigen Wallingford, CT Quality Technician Bachelor of Science degree in relevant field. Exp: 0-2 years’ |
The Quality Technician role is established to support the Simple Plex Consumables team in the Wallingford facility. Assists Quality Analysts and the QA team in our ISO compliant environment. Provides support for QC / QA activities including: hands-on evaluation of microfluidic cartridge products. $22.00 to $25.00 per hour based on experience and qualifications | 7/21/2023 |
| 4382 | Trevigen Austin, TX Advanced Research Associate Master’s degree in biology, molecular biology, biochemistry, genetics, or similar fields. Exp: 0-2 years |
Advanced Research Associates in our Research Group develop innovative nucleic acid technologies. This role will support new product initiatives by combining novel, highly multiplexed PCR technologies with analysis platforms such as qPCR, digital PCR, and long-read sequencing, and by integrating reagents, instrumentation, analysis algorithms, and software. Diagnostic disease applications span neurogenetics, (such as myotonic dystrophy, fragile X and autism spectrum disorder), oncology (liquid and solid tumors), carrier screening and other reproductive health applications. You will work in a cross-functional team to develop products and technologies that realize the next generation of molecular diagnostic tests. | 7/21/2023 |
| 4383 | Trevigen Minneapolis, MN Advanced Research Associate, Stem Cell & Gene Therapy Master’s degree in a related field. Exp: up to 2 years |
The Stem Cell and Gene Therapy Advanced Research Associate will be part of a team responsible for the design and development of novel products used in cell and gene therapy workflows, including tools for expansion, identification, and differentiation of immune cells from pluripotent stem cells. Preference will be given to candidates with experience in immunology, particularly lymphocyte cell culture and/or pluripotent stem cell culture. Desirable skills and techniques include 2D and 3D cell culture and bioassays, cell separation, immunostaining, flow cytometry analysis, and molecular biology. | 7/21/2023 |
| 4384 | Trevigen Newark, CA QC Associate B.S./B.A. in molecular biology, biochemistry, cell biology or related field. Exp: 1+ years |
We seek a highly motivated and energetic Quality Control Associate to join our Operations team. This position will be working in the Quality Control team with a focus to conduct stability studies testing and support all product testing activities from raw material to finish good product. Seeking a professional associate with the ability to learn new techniques quickly and be able to adapt to shifting priorities in a fast-paced and growing environment, while adhering to established protocols and procedures. All activities will be in compliance to ISO 13485/GMP requirement. | 7/21/2023 |
| 4385 | Tyber Medical Bethlehem, PA Quality Engineer /Senior Quality Engineer Bachelor’s Degree in Engineering or Related Science field preferred Exp: 1+ years |
The Quality Engineer or Senior Quality Engineer supports Quality Management System elements across the organization, including but not limited to the following areas: Document Control, CAPA, Control of Nonconforming Material, Quality Events, Process Validation, and more. | 7/21/2023 |
| 4386 | Universal Cells Seattle, WA Research Associate II, Core Technologies, Cell Analytics MS Degree Exp: 0-2 years |
We are seeking a highly capable, self-motivated Research Associate II for our Core Technologies Department. This individual will contribute to the further molecular engineering for our gene edited Universal Donor Cells. They will work as a key member on a fast-paced team to develop molecular and cellular assays to characterize our proprietary Universal Donor Cells. | 7/21/2023 |
| 4387 | Universal Cells Seattle, WA Research Associate II, R&D MS Degree Exp: 0-2 years |
The primary purpose of this position is to conduct studies evaluating the phenotype and function of human immune cells. This will encompass both in vitro characterization of human T cells and antigen-presenting cells, as well as functional assay development to characterize pluripotent stem cell-derived immune cells. | 7/21/2023 |
| 4388 | Universal Cells Seattle, WA Research Associate II, Core Technologies MS degree in related scientific discipline Exp: 0-2 years |
We are seeking a highly capable, self-motivated Research Associate II for our Core Technologies Department. This individual will contribute to the further molecular engineering for our gene edited Universal Donor Cells. They will work as a key member on a fast-paced team to develop molecular and cellular assays to characterize our proprietary Universal Donor Cells. | 7/21/2023 |
| 4389 | Vivex Biologics Miami, FL Quality Assurance Inspector I Bachelor degree in Life Sciences or equivalent required. Exp: 1-2 years |
The Quality Assurance Inspector is responsible for executing on a comprehensive and effective internal auditing program compliant with Standard Operating Procedures in addition to FDA, AATB, and State regulations and standards. This role also performs routine checks and verifications of the different elements of the quality system to ensure the Operation is meeting the company’s quality standards. | 7/21/2023 |
| 4390 | Frontage Hayward, CA Research Assistant- Bioanalytical Services B.S. degree in related scientific discipline. Exp: 0-3 years |
1) Assist lab work and method development 2) Follow SOP and protocol to conduct method validation and sample analysis under supervision 3) Comply with GLP regulations in lab work and documentation 4) QC review data and reports 5) Perform instrument setup, maintenance, and basic trouble-shooting under supervision 6) Strictly follow SOPs and regulations to serve as sample coordinator. | 7/21/2023 |
| 4391 | Frontage Exton, PA Lab Technician Bachelor’s degree in molecular biology, Biology, Biochemistry, Chemical Engineering, Mechanical Engineering. Exp: 1-5 years |
We are looking for a qualified Lab Technician to join our team. The role will perform and support laboratory procedures and controls within Biologics, Gene, and Cell Therapy (BGC) Department to maintain efficiency and compliance for the laboratory. The ideal candidate needs to have an entrepreneurial spirit that enables her/him to wear multiple hats as we scale-up the laboratory business. The candidate will have experience in working in a laboratory environment, preferably within biologics/or GCT lab. The candidate will be well-trained to maintain safety conditions in the lab and expected to be passionate in working in a matrix organization environment. The goal is to optimize lab compliance and maintaining the smooth running of the lab. | 7/21/2023 |
| 4392 | Frontage Secaucus, NJ Lab Technician Associate or bachelor’s degree in a biomedical discipline or related scientific discipline, or equivalent experience, or completion and certification Exp: 1 year |
Responsible for working under the guidance of the Lab Manager, Investigators; Management, Study Coordinator and Supervisor, to perform study procedures required in clinical studies conducted on behalf of sponsors at the Frontage Clinical Services. | 7/21/2023 |
| 4393 | Frontage Hayward, CA Research Assistant-ADME BS in biology, biochemistry and other related fields Exp: 0-3 years |
We are looking for a highly-motivated Research Assistant to develop and conduct biochemical and cellular assays to evaluate potential therapeutics. Experience in cell line development, ELISA, PBMC biomarker, cell culture, cellular assays, gene expression is desirable. Prior experience in ADME assays including metabolite stability, drug transporter, CYP450, PPB and measurements of physicochemical properties is preferred. The candidate needs to be proficient in assay design, trouble-shooting, data analysis and working with 96-w & 384-w plate-based assays. The candidate needs to have a good understanding of drug discovery processes and experience in a discovery project is preferred. This position requires working with an interdisciplinary team of DMPK scientists, analytical chemists and pharmacologists. | 7/21/2023 |
| 4394 | Frontage Hayward, CA Research Associate-Bioanalytical M.S. degree in related scientific discipline or B.S degree Exp: 0-3 years |
1)Execute established protocols and methods to assay small molecule compounds, their metabolites, and impurities in various chemical and biological samples. 2)Perform data analysis on LC/MS and HPLC instruments, with the ability to identify and troubleshoot inconsistencies as needed. 3) Perform analytical, pharmacokinetic/pharmacodynamic, metabolism data analysis. 4) Conduct basic method development and validation studies. 5) Conduct trouble-shooting and instrument maintenance of LC/MS. 6) Present and discuss data internally and externally. 7) Write reports under supervision. | 7/21/2023 |
| 4395 | Frontage Hayward, CA Research Associate M.S. degree in related scientific discipline. Exp: 0-3 years |
1) Perform Watson design according to Study Protocols 2) Conduct basic method development and validation studies. 3) Ability to troubleshoot and solve basic technical and instrumental issues. 4) Conducts and documents work in a regulated environment. 5) Reviews the data package and notebooks for junior chemists 6)Writing up analytical methods, protocols, and reports under supervision 7) Perform project communication with client, study director, and project management team under supervision | 7/21/2023 |
| 4396 | Frontage Concord, OH Entry Level Lab Chemist B.S. in a chemistry or related field. Exp: entry level |
This position is for an entry level lab chemist. The ideal candidate will help support studies of preclinical drug development in a GLP environment. The duties and responsibilities include: Familiarity with a majority of laboratory equipment• Basic math and chemistry skills to perform routine calculations• Strong attention to details Perform routine lab operations in a neat and clean organized manner: prepare reagents, weigh reference standards, and extract samples Shipping, receiving, proper storing, organizing, and inventory maintenance including chain of custody documentation of new test articles. Method development and troubleshooting of formulations in conjunction with Study Directors, including conducting pH, solubility, homogeneity and stability tests Document results and accurately record observations in accordance with GLPs and SOPs Conducting pH, solubility, homogeneity and stability tests The candidate should have a good chemistry background. Excellent written and oral communication skills, and the ability to manage multiple projects in dynamic environment is highly desirable. Familiarity with regulatory guidelines (GLP or GMP) is a plus. | 7/21/2023 |
| 4397 | A2 Biotherapeutics Agoura Hills, CA Manufacturing Associate Bachelor’s Degree in Biology and/or Life Sciences. Exp: 1+ years |
A2 is seeking a highly motivated Manufacturing Associate to join the team reporting to the Manufacturing Senior Associate. In this role you will work in a dynamic production environment to manufacture T cell products for clinical and launch activities. We are looking for a strong team player who wants to help us create a high performing, collaborative work environment and deliver our innovative therapies to patients. If you are seeking an opportunity that fosters growth and challenge, apply now! This is an onsite position on a 4/10 schedule at our facility in Agoura Hills, California. | 7/21/2023 |
| 4398 | Abbott Columbus, OH Associate Scientist II - Columbus, OH Bachelor's Degree required. Exp: 1-3 years |
We currently have an Associate Scientist II position open in our Columbus, OH office. The Associate Scientist II is an individual contributor that works under limited supervision. Applies subject matter knowledge; requires capacity to understand specific needs or requirements to apply skills/knowledge. Carries out fundamental or applied research in the biological or physical sciences or in mathematics requiring appreciable originality and ingenuity. | 7/21/2023 |
| 4399 | Myriad-RBM Austin, TX Laboratory Associate - Automation Bachelor’s Degree in Chemistry or a related field. Exp: 1 year |
SHIFT - MONDAY - FRIDAY 1:30PM - 10:30PM (SHIFT DIFFERENTIALS APPLY) PURPOSE Responsible for routine sample preparation duties inclusive of automated liquid handling, troubleshooting routine experiments and the preparation of solutions. | 7/9/2023 |
| 4400 | Myriad-RBM Austin, TX Associate Scientist, Assay Development - R&D Bachelor's Degree Bachelor's degree in relevant scientific discipline (some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical Exp: 1 year |
The Associate Scientist for Assay Development is responsible for assisting with experimental execution in support of assay/method development programs. | 7/9/2023 |
| 4401 | NAMSA Northwood, OH Microbiology Technologist Bachelor degree Exp: 0 years |
May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. • Accurately collects and records raw data in logbooks and on worksheets. • May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. • May be required to perform personal gowning environmental testing, and submit organisms from gowning, environmental and sterility test positives for identification and inclusion in monthly trending data, as required for specific testing as applicable. | 7/9/2023 |
| 4402 | NAMSA Northwood, OH Analytical Services Lab Technologist Bachelor’s degree in scientific discipline required. Exp: 0 years |
For bio/analytical applications, performs a variety of laboratory techniques including sample weighing and recording, preparation of standard solutions, buffers, sample preparation requiring homogenization, liquid-liquid extraction, filtration, centrifugation and pipetting, etc. • Validates bio/analytical methods and protocols adhering to GLP guidelines. • May perform routine test article/product preparation according to work instructions. • Assure testing/test article preparation/product is performed within due dates. • May prepare and maintain reagents and/or test articles as required for testing. • Performs the extraction process on prepared samples as directed by study protocol for analytical data generation. | 7/9/2023 |
| 4403 | NAMSA Minneapolis, MN Laboratory Technician An Associate or Bachelor degree in related scientific field is required. Exp: 0 years |
• Conducts sample preparation for Sponsor materials as directed by study protocols for in vivo and in vitro biocompatibility assays and pharmacology, toxicology and analytical studies. • Performs the extraction process on prepared samples in accordance to ISO, USP and JMHLW regulations as directed by study protocols for biocompatibility assays. • Receives and logs Sponsor materials for testing. Completes chain of custody documentation for test article tracking. • Prepares and maintains sterile glassware for the sample preparation process. Processes glassware through washer, autoclave and depyrogenation oven as needed. • Operates, cleans and maintains incubators, autoclaves, hoods and other equipment routinely utilized.• | 7/9/2023 |
| 4404 | NAMSA Northwood, OH Chemist Master’s degree. Exp: 0 years |
• Operates and maintains a variety of chromatographic and spectroscopic systems such as LC, LC/MS/MS, and GCMS to analyze biological and chemical elements as directed by assays or study protocols. • May order and/or stock supplies subject to approval. Maintain ancillary records (logbooks, worksheets). • Conduct routine studies independently according to work instructions. May be requested to conduct more involved studies. Routes all excursions or unusual testing occurrences to management. • Participate in the improvement of documents, test systems, quality systems, and workflow. • Responsible for review of incoming test articles and paperwork for appropriateness and accuracy and taking all concerns to management as required. • Assure testing/test article preparation/product is performed within due dates. • For bio/analytical applications; performs a variety of laboratory techniques including sample weighing and recording, preparation of standard solutions, buffers, sample preparation requiring homogenization, liquid-liquid extraction, filtration, centrifugation and pipetting, etc | 7/11/2023 |
| 4405 | NJ Biopharmaceuticals Princeton, NJ R&D - Bioconjugation B.S. in Biochemistry, Protein Chemistry, or other related fields. Exp: 0-3 years’ |
Associate Scientist Job Responsibilities Under department supervision, plan, setup, monitor and purify bioconjugation reaction using aseptic techniques; characterize and identify bioconjugates using LC-MS, HPLC and/or Capillary Electrophoresis; maintain a detailed lab notebook; maintain equipment, and provide lab support; provide data in a detailed report; Plan and execute daily and weekly schedule; perform safe lab practices; comply with Site safety protocols and Site Standard Operating Procedures (SOPs). Perform additional duties as required. | 7/12/2023 |
| 4406 | NJ Biopharmaceuticals Princeton, NJ Associate Scientist, Process R&D, Chemistry B.S. in Chemistry. Exp: 0-5 years’ |
Job Responsibilities Support Senior and Principal Scientist – In hands-on scalable processes in kilo-lab for manufacturing pharmaceutical intermediates and Active Pharmaceutical Ingredients (APIs) and highly potent APIs (HPAPIs) after training with supervision For safely optimizing synthetic organic chemistry processes for scale up into large glassware, pilot plant tech transfers projects for APIs, and HPAPIs under supervision Running samples for characterization on NMR, MS, HPLC In pilot scale purifications using Teledyne ISCO purification and Torrent system Carry out literature searches and mine information for ongoing work from search Maintain equipment, chemical inventory, and provide lab support Execute daily and weekly tasks assigned Perform safe lab practices; comply with Site safety protocols and Site Standard Operating Procedures (SOPs) Maintain a detailed lab notebook Perform other duties as required | 7/12/2023 |
| 4407 | Oakwood Labs Oakwood Villiage, OH Chemist Bachelor’s degree in chemistry, biology, or related discipline. Exp: 0+ years |
Oakwood Laboratories is looking to add to their Analytical Chemistry Team! This is an excellent entry level opportunity for those interested in working at a technology-based pharmaceutical company. There will be on the job training rotations in the research and development lab and the quality control chemistry lab. You will gain hands-on experience analyzing and interpreting data for excipients, polymers, active ingredients, and finished pharmaceuticals utilizing advanced analytical instrumentation. You will work as part of small multi-disciplinary technical teams on both immediate and sustained release drug development projects in various stages of development including early proof of concept, supporting pharmacokinetic and clinical studies, technical transfer activities, and supporting commercial product manufacturing. You will have direct input on solving complex problems and contributing to project success. Become part of the Oakwood Labs team and advance your career with an industry leader in injectable pharmaceutical development.Oakwood Laboratories is looking to add to their Analytical Chemistry Team! This is an excellent entry level opportunity for those interested in working at a technology-based pharmaceutical company. There will be on the job training rotations in the research and development lab and the quality control chemistry lab. You will gain hands-on experience analyzing and interpreting data for excipients, polymers, active ingredients, and finished pharmaceuticals utilizing advanced analytical instrumentation. You will work as part of small multi-disciplinary technical teams on both immediate and sustained release drug development projects in various stages of development including early proof of concept, supporting pharmacokinetic and clinical studies, technical transfer activities, and supporting commercial product manufacturing. You will have direct input on solving complex problems and contributing to project success. Become part of the Oakwood Labs team and advance your career with an industry leader in injectable pharmaceutical development.Oakwood Laboratories is looking to add to their Analytical Chemistry Team! This is an excellent entry level opportunity for those interested in working at a technology-based pharmaceutical company. There will be on the job training rotations in the research and development lab and the quality control chemistry lab. You will gain hands-on experience analyzing and interpreting data for e | 7/13/2023 |
| 4408 | Oakwood Labs Oakwood Villiage, OH Chemical Engineer/ Biomedical Engineer Bachelor of Science, Masters, or PhD Degree in Biomedical or Chemical Engineering, or Chemistry or closely related science field with chemistry and ma Exp: one year |
This is an excellent entry-level opportunity for those interested in working at a technology-based pharmaceutical company. The successful incumbents will work in our product development function and: Perform pre-formulation laboratory experiments and studies Perform process scale-up from laboratory to pilot laboratory Perform process scale-up from pilot laboratory to manufacturing facility Work on technology transfer activities. | 7/13/2023 |
| 4409 | Patheon Lexington, MA Process Engineer I Bachelor’s degree in Mechanical, Chemical, Biochemical/Biomedical, Electrical, or Automation Engineering, or related field of study Exp: 1 year |
DUTIES: Support the manufacturing operations team to optimize overall equipment efficiency. Support the procurement of new systems, oversee FATs, SATs and Qualification of these new systems, layout configuration for new clients, and PFD development and equipment readiness for tech transfers. Execute process equipment improvement projects stemming from process changes/optimizations, CAPAs, and new capacity demands including compliance item. Drive continuous improvement and operational excellence culture through self-detecting and self-correcting processes and systems and instilling strong ownership and accountability. Ensure high levels of communication with team, support resources, and management regarding issues and resolutions. | 7/14/2023 |
| 4410 | Patheon Asheville, NC Engineer II, Mechanical Master’s degree in Mechanical Engineering, or related field of study. Exp: 1 year |
DUTIES: Develop specifications for system-level, subsystem and component performance based on customer needs and product requirements. Develop the optimal design through Computer Aided Engineering (CAE), Tradeoff Analysis, Technology Assessment, Failure Modes and Effects Analysis (FMEA). Develop and execute test plans to validate the performance of newly developed products by utilizing design for reliability tools and performance sensitivity analysis. Support manufacturing to evaluate and troubleshoot issues and recommend solutions to maintain production uptime. Work with Regulatory Affairs team members to design products that meet and acquire the required global product approvals and certifications such as, FDA, UL, CE, CSA, NSF, and Energy Star. Identify and implement design changes that improve user experience, quality, manufacturability, serviceability and sustainability of CTT products. | 7/14/2023 |
| 4411 | Patheon Lexington, MA QC Scientist I Bachelor’s degree in science required ; preferably Microbiology or Biology Exp: 1 year |
Location: Lexington, MA Shift: Days Wednesday-Saturday (10 hour shift) (Training will be conducted Monday -Friday between 8:00am-5:00pm) How you will make an Impact... The QC Microbiology Scientist I will be an integral member of the group in the cGMP compliant QC Microbiology Laboratory supporting manufacture of biological products. The key focuses will be to assist in the timely completion of in-process and release testing of clinical and commercial grade biopharmaceuticals, qualification/validation of analytical methods for support of viral vector cGMP compliant manufacturing and the transfer and validation of methods from clients. The incumbent will act as an analyst in the lab by performing and providing support for functional aspects of the facility such as environmental monitoring (EM), microbiological testing (bioburden, bacterial endotoxin testing, growth promotion, biological indicators, stock cultures), media fills, water testing and validation support. The incumbent will be expected to write and technically interpret controlled documents and reports, and review data produced by self and initiate investigations | 7/14/2023 |
| 4412 | Patheon San Francisco, CA Cell Therapy Specialist Bachelor’s or Associates degree in a technical field desired. Exp: 1+ years |
Apply all available resources to achieve the department goals. Take accountability for results and responsibility for the decisions made during all shifts. Hence, must ensure that the role is clear Execution of manufacturing batch records, work instructions and/or SOPs on a day-to-day basis and a focus on proactive ‘right the first time’ executions. Assist with batch record reconciliation and timely documentation. Performance of all manufacturing activities in clean room (ISO 7) environment with specialized sterile gowning. Execution of cell manufacturing and cell processing activities in closed systems and maintaining aseptic technique during processing to ensure highest integrity, viability and sterility of cellular product until release. Work as a part of the team to execute all necessary GMP runs for cell manufacturing in an accurate and timely manner Perform accurate and error-free calculations of cell concentrations, cell and media dilutions and cell viability throughout the entire cell manufacturing process workflow. Able to execute all Department functions, such as maintaining suite, supplies, equipment, logbooks and data in accordance with site SOPs and policies. Documentation of all activities to meet cGMP requirements. Execute document reviews and revisions. Daily record review, tasks, and databases. Actively provide feedback. Perform timely consumption of materials and completion of quality documentation in appropriate systems | 7/14/2023 |
| 4413 | PCI Pharma Services Bedford, NH Formulation Technician I (Wed to Sat 6 AM to 4:30 PM) BS degree in Chemical Engineering/ Bio Chemistry or other industry related discipline is preferred. Exp: 1-2 year’s |
This position will have the primary responsibility for daily formulation activities to ensure schedule activities are completed, formulation materials and equipment are maintained, as well as the responsibility for performing corrective and preventative actions. As a secondary function, provide troubleshooting expertise for manufacturing of products both internally and externally of the company. | 7/14/2023 |
| 4414 | PCI Pharma Services Bedford, NH Formulation Technician I (Sun-Wed, 6:00 AM-4:30 PM)-3 BS degree in Chemical Engineering/ Bio Chemistry or other industry related discipline is preferred. Exp: 1-2 year’s |
This position will have the primary responsibility for daily formulation activities to ensure schedule activities are completed, formulation materials and equipment are maintained, as well as the responsibility for performing corrective and preventative actions. As a secondary function, provide troubleshooting expertise for manufacturing of products both internally and externally of the company. | 7/14/2023 |
| 4415 | PCI Pharma Services Bedford, NH Plant Engineer l BS in Chemical, Mechanical, or other Engineering degree from an accredited university. Exp: 0-2 years’ |
The Plant Engineer I provides engineering support throughout the various manufacturing facilities in areas such as process equipment improvements, technological advancements, capital projects, existing manufacturing equipment, cost improvements, facility maintenance, safety and environmental regulation. Demonstrate good engineering, effective collaboration, partnering and teamwork skills when interacting with internal and external resources. | 7/14/2023 |
| 4416 | PCI Pharma Services Madison, WI Formulation Technician II BS degree in related field of study is preferred. Exp: 1 year |
This position will have the primary responsibility for daily formulation activities to ensure scheduled activities are completed, formulation materials and equipment are maintained, as well as the responsibility for performing corrective and preventative actions. As a secondary function, provide troubleshooting expertise for manufacturing of products both internally and externally of the company. | 7/14/2023 |
| 4417 | PCI Pharma Services Madison, WI Chemist I Bachelor of Science in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study Exp: 0-3 years |
This position will have responsibility to support various activities in the Quality Control Laboratory. This includes testing the following sample types R&D, in-process, finished product, stability, as well as raw materials. Job duties may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management. | 7/14/2023 |
| 4418 | PCI Pharma Services Philadelphia, PA Process Engineer Bachelor's Degree in Mechanical or Packaging Engineering or related field Exp: 1-5 years |
The Process Engineer is responsible for identifying and mitigating packaging issues for existing business through strong engineering and process improvement methods. Provide technical leadership for new product launches. Lead continuous improvement activities. Secondary tasks include specify, purchase, and commission new equipment and manage capital finances. Provide technical support for new business (Sales/Business Development Support). All activities are focused around technical and operational support to the production, maintenance, and support staffs in the areas of process improvement, equipment modification and optimization, safety, and quality improvement, and increasing throughput. This is achieved through individual effort and facilitation of teams, tracking and analysis metrics, strong understanding and utilization of good engineering practices, project management, and the use of Lean Six Sigma techniques. Additionally, the Process Engineer will be responsible determining staffing, equipment needed, equipment purchase, equipment installation, component layout and line layout | 7/14/2023 |
| 4419 | PCI Pharma Services Philadelphia, PA Process Engineer I-2nd Shft Bachelor's Degree in mechanical, packaging engineering, or in a related field of study. Exp: 1-5 years |
We are looking for a dedicated process engineer to identify and mitigate packaging issues for existing business through strong engineering and process improvement methods. As a process engineer, you will provide technical leadership for new product launches and lead continuous improvement activities. Secondary tasks include specify, purchase, and commission new equipment, manage capital finances, and provide technical support for new business (Sales/Business Development Support). All activities are focused around technical and operational support to the production, maintenance, and support staffs in the areas of process improvement, equipment modification, optimization, safety, quality improvement, and increasing throughput. This is achieved through individual effort, facilitation of teams, tracking analysis metrics, strong understanding and utilization of good engineering practices, project management, with the use of Lean Six Sigma techniques. The process engineer should also have excellent organizational and leadership skills to determine staffing projections, equipment needs, equipment purchase, equipment installation, component layout, and line layout | 7/14/2023 |
| 4420 | KARL STORZ Endoscopy-America Franklin, MA Project Engineer BS Degree in a Technical / Engineering discipline. Exp: 1+ years |
The purpose of this position is to develop processes to enable KARL STORZ to manufacture products with specific focus on injection molding and manual/semi-automated assembly techniques. This position will ensure the relevant infrastructure, equipment, tooling & fixturing is designed, implemented and qualified to help introduce new products and processes. | 7/14/2023 |
| 4421 | KARL STORZ Endoscopy-America Charlton, MA Test Engineer II MS degree in Electronics Technology/Engineering or related field. Exp: 0-3 years |
Under minimal supervision, provides design verification support for Karl Storz products to verify that they meet quality standards, including the design and execution of approved verification procedures, the execution of studies and troubleshooting in support of design engineering, and the training of other test engineers. | 7/14/2023 |
| 4422 | KARL STORZ Endoscopy-America Goleta, CA Test Engineer II-Contract Temporary MS degree in Electrical Engineering, Mechanical Engineering, Software Engineering, Computer Engineering, Biomedical Engineering, or related field. Exp: 0-3 years’ |
Design Verification Test Engineer II (temporary – 1 year) Shift: Mon - Thur, 10 hour Day. As a member of the Design Verification team in Goleta, CA, the Test Engineer II position holds key responsibilities for ensuring KARL STORZ’s line of video imaging systems continue to maintain their reputation among surgeons and medical staff for delivering world-class quality. Please note that this is a temporary position to support a large development project. | 7/14/2023 |
| 4423 | Agen Tus Therapeutics Lexington, MA Manufacturing Associate, Cell Therapy Bachelor’s Degree in Life Sciences or related Engineering field Exp: 1-3 years |
· Prepare equipment and materials including Clean-Out-of-Place and Sterilization. · Operate and monitor manufacturing equipment for production of biological products under minimal supervision. · Execute routine and complex production processes including, but not limited to, cell isolation, expansion, stimulation, harvest, and final fill operations. · Perform responsibilities according to procedure while maintaining compliance and safe operating practices. · Ability to troubleshoot and think innovatively to resolve process issues. · Receive and distribute supplies and maintain inventory in the Manufacturing area. · Provide feedback to supervisor on recommendations for procedural and process improvements. · Utilize process knowledge to influence positive change during the review and revision of Standard Operating Procedures (SOP’s) and Batch Records. · Maintain documentation according to current Good Manufacturing Practices (cGMP’s).· | 7/14/2023 |
| 4424 | Agen Tus Therapeutics Lexington, MA Senior Research Associate/Associate Scientist, Immuno-oncology MSc in fields such as biochemistry, molecular biology, immunology, cancer biology, or related discipline is required. Exp: 1+ years |
The successful candidate will have a strong background in cell biology, immunology, molecular biology, and/or oncology research. He/She will work closely with discovery scientists to advance research stage programs into early clinical development in the field of cancer cell therapy/immunotherapy, providing both scientific and technical expertise. | 7/14/2023 |
| 4425 | PolyPeptide Group Torrance, CA Production Chemist I BS in Chemistry, Biochemistry, Biology or related science field Exp: 1+ years |
Production Chemist is responsible for completing tasks & assignments in accordance with established processes & methodologies; synthesize peptides, intermediates, & processing from initial stage. | 7/14/2023 |
| 4426 | Prominex San Diego, CA Research Associate I/II Master’s degree in Science Exp: 0-2 years |
Prominex Inc. is a startup molecular diagnostic company with an experienced team of passionate and energetic scientists driven to create fast and affordable molecular diagnostic solutions across the globe. We are focused on infectious disease assays in point-of-care and home-based settings. We are looking for an enthusiastic and dedicated Research Associate to implement and execute analytical and scientific experiments to drive Product Development. Demonstrates high degree of organization and planning and the ability to apply scientific principles to plan out and execute experiments involving a variety of laboratory methods. This individual demonstrates technical proficiency, high degree of organization and planning and the ability to apply scientific principles. | 7/14/2023 |
| 4427 | Psomagen Cambridge, MA or Rockville, MD, MA CES Lab Technician (MD or MA) Bachelor’s degree required. Biology majors or relevant major are preferred. Exp: 1+ years |
Psomagen, Inc. is a fast-growing biotechnology company with a focus on DNA sequencing. We are currently searching for a motivated Lab Technician who is able to work full-time at our branch in Rockville (MD) or Cambridge (MA). It is the responsibility of the laboratory technician to perform routine tests using laboratory equipment. Paid training will be provided but the job requires knowledge of basic science to learn techniques/methods. It is important that the technician also understands the role of senior lab members and is able to accept constructive guidance. This role will be based in our lab in Rockville, Maryland or Cambridge, Massachusetts | 7/14/2023 |
| 4428 | Psomagen Cambridge, MA or Rockville, MD, MA Clinical Lab Scientist [MD or MA] Bachelor’s degree required. Biology majors or relevant major are preferred. Exp: 1+ years |
Psomagen, Inc. is a fast-growing biotechnology company with a focus on DNA sequencing. We are currently searching for a motivated Clinical Lab Scientist who is able to work full-time at our branch in Rockville (MD) or Cambridge (MA). It is the responsibility of the Clinical Lab Scientist to perform routine tests using laboratory equipment. Paid training will be provided but the job requires knowledge of basic science to learn techniques/methods. It is important that the Clinical Lab Scientist also understands the role of senior lab members and is able to accept constructive guidance. This role will be based in our lab in Rockville, Maryland or Cambridge, Massachusetts. | 7/14/2023 |
| 4429 | Psomagen Rockville, MD NGS Laboratory Technician/Scientist/Manager Bachelor’s degree required. Biology majors or relevant major are preferred. Exp: 1+ years |
We are looking for a meticulous clinical laboratory lab technician/associate/scientist to join our team at our NGS (next-generation sequencing) lab team. An ideal candidate will be able to perform laboratory tests, experimental procedures and effectively monitor lab inventory supplies as well as equipment. This position will be based in the Psomagen office in Rockville, Maryland (on-site). | 7/14/2023 |
| 4430 | RayzeBio Indianapolis, IN Quality Control Chemist MS in Chemistry, Science, or relevant field Exp: 1+ years |
Reporting to the Sr. Manager of Quality Control, the Quality Control Chemist will help support the establishment of a new Quality Control laboratory which supports RayzeBio’s Radiopharmaceutical manufacturing facility in Indianapolis. The Quality Control Chemist will be responsible and/or providing support for the installation, commissioning, qualification, and validation of analytical and radiochemical equipment for the QC lab. Upon establishment of the laboratory and program, this position will utilize a wide range of analytical and radiochemical analyses to support the advancement and release of novel targeted radiopharmaceuticals from the R&D phase through clinical development to GMP commercial radiopharmaceutical production. Specifically, the quality control chemist will support the release of manufactured radiopharmaceuticals to support RayzeBio’s clinical and commercial programs. | 7/14/2023 |
| 4431 | Resilience Alachua, FL Quality Control Analyst I Bachelor's Degree Exp: 1+ years |
Performs simple/compendial assays Supplies inventory and lab organization In-process and finished product samples to include bioburden, bacterial endotoxin, and sterility. Raw material testing for specific microbial requirements. Environmental Monitoring of cleanrooms and dynamic processes including viable air sampling, surface sampling, non-viable air sampling, and personnel monitoring. Sampling and analysis of purified water, Water for injection and clean steam. Sampling and analysis of compressed air and gases. Biological indicator receipt, issuance, and analysis. Media fill inspection Growth promotion of media and media fill units. Perform microbial identifications, evaluating and interpreting results to identify objectionable organisms from environmental monitoring and product testing. Demonstrate the ability to understand and interpret test results and use the results to make a decision with regard to acceptance of the associated criteria and requirements. | 7/14/2023 |
| 4432 | Resilience Waltham, MA Senior Research Associate, Upstream Process Development, Biologics Masters Degree Exp: 1+ years |
RESILIENCE is seeking a talented Sr. Research Associate in Upstream Process Development for the Biologics Franchise who will: Function as a key member of the Upstream Process Development group in Waltham, MA Focus in fed-batch and perfusion bioreactor operations Assist in building out and leading upstream operation of the Pilot lab to enable Tox Lot production Work collaboratively with other leaders throughout the network to advance objectives, priorities, and disruptive technologies Operate with the mission to transfer and develop robust, scalable, cost-effective therapeutic upstream bioprocesses for RESILIENCE Biologics partners and drive development and implementation of innovative internal technology platforms | 7/14/2023 |
| 4433 | Rocket Pharmaceuticals Cranbury, NJ Research Associate I, Nonclinical R&D B.S. in relevant Biological Sciences field Exp: 1-2 years |
Rocket is seeking an individual who will work within the R&D team supporting nonclinical studies to further understand and characterize viral vector constructs for potential therapeutic application in support of Rocket’s gene therapy pipeline. The ideal candidate will have a strong Molecular Biology background, will be highly collaborative, and will adhere to established processes, policies, and quality systems for conducting experiments and reporting data from basic research studies. This is an exciting opportunity to actively contribute to ongoing translational research efforts aimed at developing potential therapeutics for life-threatening diseases utilizing gene therapy. | 7/14/2023 |
| 4434 | Rocket Pharmaceuticals Cranbury, NJ Associate Scientist, Quality Control BS in Biology, molecular biology, virology, Life Sciences or equivalent Exp: 0 - 2 years |
We are seeking an Associate Scientist, Quality Control with the responsibility to support clinical manufacturing of a range of Gene Therapy products. Technical proficiency in analytical methodology for drug substances and drug products is required for gene-based products. | 7/14/2023 |
| 4435 | Sanaria Rockville, MD Research Associate, Cell Culture BS in biology, biotechnology, microbiology, or a related discipline Exp: 1-2 years |
We are currently seeking a Research Associate (BS) with cell culture experience to join our Gametocyte Production group. The Research Associate will be involved in many aspects of Sanaria’s PfSPZ vaccine research and cGMP manufacturing process. Ability to work on the maintenance of malaria parasite cultures and multiple simultaneous tasks is essential. The RA will participate in research projects targeted to efficiency and scaling up. The selected candidate must have weekend availability for some projects. | 7/14/2023 |
| 4436 | Sanaria Rockville, MD Research and Manufacturing Associate, Mosquito and in-Vitro Production Bachelor’s degree in biology, chemistry, biotechnology, entomology or a related field. Exp: 1+ years |
We currently have an opening for a Research Associate or Sr. Research Associate in our Mosquito and in-Vitro Production group. The Research and Manufacturing Associate will maintain cells in culture, use 3D culture, fluorescent staining methods and standard membrane feeding assays, etc. The Associate will also be required to perform key operations during PfSPZ Vaccine manufacture that will include microscopic assessments of sporozoite attenuation or enumeration, sporozoite hepatocyte invasion assays, and also mosquito production, mosquito dissection, or other component procedures. The Associate will conduct research towards malaria parasite’s sporogonic development in vitro and in mosquitoes, | 7/14/2023 |
| 4437 | SCA Pharma Windsor, CT Chemist I Bachelor’s degree in Chemistry, Biology, Chemical Engineering or Life Sciences (Preferred in Chemistry). Exp: 1+ years |
The Quality Control (QC) Chemist I is an entry level position for individuals who use their understanding of Analytical Chemistry to perform the basic and routine experiments including generation and analysis of data in a cGMP laboratory. | 7/14/2023 |
| 4438 | SCA Pharma Little Rock, AR Incoming Quality Assurance (IQA) Specialist Bachelor’s degree in life sciences, engineering, or related discipline preferred Exp: 1+ years |
The Incoming Quality Assurance Specialist will ensure that critical and key raw materials and supplies that are received meet raw material specifications set forth by SCA Pharmaceuticals and have appropriate certificates of analysis and certificates of conformance prior to releasing to inventory. These responsibilities will be performed at the production site as well as the warehouse site. In addition, the individual in this position will be responsible for maintaining and improving existing processes, as well as assisting in the design and development of new processes, in the areas of Incoming Quality Assurance release requirements, trending of received material specifications, assisting with recalls of raw materials, assisting with raw material specification creation, and coordinating raw material specification changes. | 7/14/2023 |
| 4439 | PerkinElmer Pennington Reserve at Upper Provide, PA Research Technician Bachelor’s Degree in a scientific field. Exp: 1+ years |
Job Responsibilities: Weekly liquid nitrogen filling of NMRs Perform morning startups of NMRs Perform equipment user-level upkeep, minor troubleshooting, general laboratory prep work, inventory checks, and scheduled equipment quality checks. Notifies supervisor and/or manager when deficiencies are noted. Participate in audits and inspections and provide input, as requested. Support general technical lab activities as needed (ex: replacing water in water baths / incubators, removing expired chemicals in the lab, ensuring that filters are changed on freezers, etc.) Maintain training and compliance in areas of health and safety, security, environmental and operational aspects of daily activities in the working environment | 7/3/2023 |
| 4440 | PerkinElmer Annapolis, MD Research Specialist Bachelors Degree in science or chemistry. Exp: 6 months |
Responsibilities: Provide high quality laboratory support to the Cell Services team. Grow, maintain, and cryopreserve contamination-free mammalian cells (suspension & adherent). Preparation of cell pellets for histological processing. Provide daily, vials of tested, frozen cell lines to scientists. Isolate and cryopreserve primary PBMCs and further cell subsets from both whole blood and leukopaks. Isolate a variety of cell types from fresh blood daily in a timely manner. Isolate serum from whole blood. Maintain sterile technique while culturing isolated primary cells. Perform established flow cytometry QC protocols on a routine basis and analyze results. Generate and analyze data with the highest Data Integrity standards to include identifying and reporting unusual results/outcomes. Operate and maintain laboratory instrumentation including Mycoplasma onsite testing & clean-up as warranted. | 7/3/2023 |
| 4441 | PerkinElmer Annapolis, MD Media Prep Specialist Bachelor’s Degree in a chemistry, biology, or other relevant discipline. Exp: 1+ years |
Responsibilities: Prepare high quality media, buffer, and reagents according to a regularly occurring schedule as well as special requests. Track & document shelf life of media mixes, and plan for re-occurring mix preparation Follow SOPs, protocols, and other guidelines as it relates to the preparation of reagents and buffers Quality control testing of these materials to ensure products are free of contaminations and are formulated appropriately Maintain relevant lab supplies and materials, manage stock solutioninventory and prepare as needed Write, maintain, and troubleshoot experimental protocols Analyze, synthesize, and communicate data to both technical and non-technical colleagues and collaborators Be able to interact with colleagues in other functions and department to solve technical problems Perform general laboratory tasks, which may includeupkeep of equipment, stocking of consumables, glass washing, and overall lab upkeep Proficient technical skills required upon completion of relevant training: balance usage, pH meters, liquid-transfer devices | 7/3/2023 |
| 4442 | Sanofi Waltham, MA mRNA -Senior Research Associate, Purification (Plasmid Production) - Vaccine MS in biochemistry, chemistry, chemical or biomedical engineering. Exp: 0-2 years |
We are seeking a highly motivated and scientifically rigorous individual to join the Plasmid Production Pilot team. You will focus on execution and scale-up of a robust pDNA production process focusing on bacterial cell lysis, supercoiled plasmid DNA linearization, and purification for preclinical linearized plasmid DNA production, with the ultimate goal of transferring at scale methods to either the internal or external manufacturing team for mRNA drug substance with applications towards vaccine development. Evaluate and implement purification technology and optimize existing techniques and workflows. Support the execution and optimization of plasmid DNA purification, problem solving. Design and execute decision-quality research; prepare/draft SOPs, technical reports, batch record, and presentations to management and other stakeholders. Work independently, pro-actively, and be an impactful contributor to project teams. Function in highly collaborative cross functional teams. Execute ~20 batches per year. | 7/4/2023 |
| 4443 | Sanofi Waltham, MA mRNA -Senior Research Associate, Plasmid Production (Upstream Fermentation) - Vaccine MS in cell or molecular biology, biochemistry, chemical or biomedical engineering, biotechnology Exp: 0-2 years |
We are seeking a highly motivated and scientifically rigorous individual to join the Plasmid Production Pilot team. You will focus on execution and scale-up of a robust pDNA production process through fermentation, cell lysis extraction, linearization, and purification for preclinical linearized plasmid DNA production, with the ultimate goal of transferring at-scale methods to either the internal or external manufacturing teams for mRNA drug substance manufacturing team with applications towards vaccine development. Evaluate, and implement new biology and purification technology and optimize existing techniques and workflows, including the execution and optimization of plasmid production, problem solving. Execute decision-quality research; prepare/draft SOPs, batch record, and presentation to Plasmid Production Pilot team. Work independently, pro-actively, and be an impactful contributor to project teams. Function in highly collaborative cross functional teams. Execute ~20 batches per year. This will be primarily a lab-based position. | 7/4/2023 |
| 4444 | Sanofi Cambridge, MA Senior Research Associate, Dupixent Research, Immunology and Inflammation Therapeutic Area Master’s Degree Exp: 1 year |
The Type 2 Inflammation and Dupixent Research cluster in the Immunology and Inflammation therapeutic area within Sanofi is seeking an experienced and highly motivated scientist to join their team. The candidate will help to expand our mechanistic understanding of Dupixent and maximize its value through execution of dedicated research studies. A successful candidate will have a background in immunology and an ability to integrate into multiple projects, contributing technical in vitro and in vivo skills. The candidate must be driven, resourceful, and able to work independently. Excellent organizational skills in management of data, reagents and equipment are essential. The candidate will participate in regular team meetings and present results, interpret data, and formulate conclusions. Teamwork, collaboration with colleagues across disciplines and excellent verbal and written communication skills are critical. | 7/4/2023 |
| 4445 | Sanofi Cambridge, MA Senior Research Associate Immunology - Vaccines - VIE Contract (W/M) Master’s Degree in Immunology, Virology, Biochemistry or Physical Science or applied science field Exp: 1 year |
We are looking for: Senior Research Associate Immunology - Vaccines - VIE Contract (W/M) Target start date: 01/09/2023 Responsibilities: Laboratory research/Assay development/Immunomodels development With limited oversight, collaborate on project design, planning and execution of studies With limited oversight, exercise creativity when devising new protocols and/or optimizing assays for stronger performance With manager oversight, design and perform experiments that comply with SOPs and maintain scientific norms (contains appropriate positive and negative controls, replicates, standards, etc.) to appropriately achieve goals set forth in study plans Exercise knowledge in selection, design, execution, and analysis of experiments that contribute to project goals Perform a wide variety of technical procedures and operate a wide variety of lab instrumentation/computer platforms related to Immunology Support the development and optimization of automation protocols for immune assays Participate in monitoring and maintaining facility related aspects of the lab and lab equipment as needed | 7/4/2023 |
| 4446 | Siemans Healthineers Newark, DE Laboratory Technician 2-Weekend Shift Bachelor’s degree or equivalent required on one or more of the following fields: Biochemistry, Biology or Chemistry Exp: 1 year |
This is a role well suited to an ambitious professional, looking for the next step in their career. As a Laboratory Technician, you will be responsible for: • Works within Specialty Reagents In-Vitro Production team to produce antibody raw material. • Responsibilities include preparation of nutrient supplements, equipment set up, autoclave operation, as well as operating equipment that is needed to harvest and purify antibody material. • Responsible for monitoring and controlling processes while maintaining accurate quality records. • Working understanding of Windows environment and related software • Work in a control environment and complete tasks aseptically to ensure no microbial contamination | 7/5/2023 |
| 4447 | Siemans Healthineers Walpole, MA Laboratory Technicians Bachelor degree with a concentration in science (Biochemistry, Biology, Chemistry, etc.) Exp: 0-1 years |
Do you want to join us in helping to fight the world’s most threatening diseases and enabling access to care for more people around the world? At Siemens Healthineers, we pioneer breakthroughs in healthcare. For everyone. Everywhere. We offer you a flexible and dynamic environment with opportunities to go beyond your comfort zone in order to grow personally and professionally. Sound interesting? Then come and join our Walpole Reagent Manufacturing team as a Laboratory Technician in: Reagent Manufacturing Technicians, QC Technicians, or QC Microbiology Technicians. | 7/5/2023 |
| 4448 | Siemans Healthineers Johnson City, TN Test Engineer, R&D - Level 1 Bachelor’s in Electrical Engineering, Computer Engineering, or Computer Science (listed in priority order) Exp: 0-3 years |
The Test Engineer participates in analyzing, developing, implementing processes, technologies, and systems for the testing of automation products. May work with hardware and software design to perform fault insertion tests or development tests of prototype products. The Test Engineer reports to the Engineering Manager / Project Leader working on Functional Safety projects and is an individual contributor working directly within the test team under the direction of the Technical Team Lead Engineer. | 7/5/2023 |
| 4449 | Siemans Healthineers Mishawaka, IN Scientist I Bachelor’s degree in a science related field, preferably chemistry or biology. Exp: 1-2 years |
This is a role well suited to an ambitious professional, looking for the next step in their career. As a Scientist 1, you will be responsible for: • Performs a wide variety of assignments according to established procedures, including but not limited routine and moderate tests/analyses, data review and analysis, as well as solution preparations • Completes preparation of product release reports • Reviews documentation generated by the lab prior to release to ensure accuracy and completeness • Provides inputs used for the purpose of control charting and trending of data collected through the release process • Ensures compliance of current procedures and processes and as needed reviews and updates documentation • Communicates issues encountered in the lab to initiate the investigation phase as well as aids in troubleshooting process with the lab supervisor | 7/5/2023 |
| 4450 | Siemans Healthineers Mishawaka, IN Scientist I Bachelor’s degree in a science related field, preferably chemistry or biology Exp: 1-2 years |
This is a role well suited to an ambitious professional, looking for the next step in their career. As a Scientist 1, you will be responsible for: • Performs a wide variety of assignments according to established procedures, including but not limited routine and moderate tests/analyses, data review and analysis, as well as solution preparations • Completes preparation of product release reports • Reviews documentation generated by the lab prior to release to ensure accuracy and completeness • Provides inputs used for the purpose of control charting and trending of data collected through the release process • Ensures compliance of current procedures and processes and as needed reviews and updates documentation • Communicates issues encountered in the lab to initiate the investigation phase as well as aids in troubleshooting process with the lab supervisor • Participation in validation activities for equipment qualifications and process implementations | 7/5/2023 |
| 4451 | Siemans Healthineers Lexington, MA Process Engineer I Bachelor’s degree in Mechanical, Chemical, Biochemical/Biomedical, Electrical, or Automation Engineering. Exp: 1 year |
Support the manufacturing operations team to optimize overall equipment efficiency. Support the procurement of new systems, oversee FATs, SATs and Qualification of these new systems, layout configuration for new clients, and PFD development and equipment readiness for tech transfers. Execute process equipment improvement projects stemming from process changes/optimizations, CAPAs, and new capacity demands including compliance item. Drive continuous improvement and operational excellence culture through self-detecting and self-correcting processes and systems and instilling strong ownership and accountability. Ensure high levels of communication with team, support resources, and management regarding issues and resolutions | 7/5/2023 |
| 4452 | Jordi Labs Mansfield, MA Chemist Master’s degree in chemistry or other closely related field. Exp: one year |
Job duties: 1) Prepare technical reports 2) Interpret gas chromatograph mass spectrometry (GCMS) and liquid chromatograph mass spectrometry (LCMS) results with a high level of proficiency 3) Interpret chromatographic data including high performance liquid chromatography (HPLC), gas chromatography (GC), and gel permeation chromatography (GPC) results 4) Combine results from multiple techniques to identify unknown chemical compounds 5) Quantify chemical components using HPLC and GC results 6) Work with a team of scientists to design and implement analytical strategies 7) Perform or oversee complex analytical strategies with an emphasis of MS and chromatography | 7/5/2023 |
| 4453 | Jordi Labs Mansfield, MA Analytical Laboratory Chemist Bachelor’s degree in Science preferred. Exp: One years |
Laboratory Tasks Sample Preparation Differential Scanning Calorimetry (DSC) Thermal Gravimetric Analysis (TGA) Gel Permeation Chromatography (GPC) Fourier Transform Infrared Spectroscopy (FTIR) Solid Phase Extraction (SPE) Preparation of Technical Reports | 7/5/2023 |
| 4454 | Kriya Therapeutics Morrisville, NC Analyst I, Quality Control Microbiology BS in Microbiology or other related field. Exp: 0 – 2+ years |
We are seeking a Quality Control (QC) Analyst I to join the QC Microbiology team at Kriya. This individual will play a critical role in the qualification of Kriya’s Manufacturing Facility, including Environmental and Compressed Gas Monitoring. In addition to, this individual will support sample control, raw material release, and microbiology laboratory testing. | 7/5/2023 |
| 4455 | Krystal Biotech Pittsburgh, PA Research Associate / Senior Research Associate, Platform Development Bachelor’s or Master’s in Biological Sciences or related scientific discipline. Exp: 1+ years |
The Platform Development group is seeking a highly motivated and innovative Research Associate or Senior Research Associate to join our multidisciplinary team. To be successful, the candidate should demonstrate basic knowledge in fundamental cloning and molecular biology techniques, tissue culture, and virology, show curiosity, initiative, and the ability to work well in a timeline-driven environment. | 7/5/2023 |
| 4456 | Krystal Biotech Pittsburgh, PA Research Associate, Analytical Development Bachelor’s degree (Biology, Biochemistry, Chemistry, or related science) Exp: 0-2+ years |
Krystal Biotech, Inc is seeking a highly motivated Research Associate to perform high quality analytical development to support research for gene therapy products. This position will be laboratory based. | 7/5/2023 |
| 4457 | Krystal Biotech Pittsburgh, PA Process Validation Associate / Engineer Bachelors’ Degree in Chemical Engineering, Biomedical Engineering Exp: Associate: 1+ yr |
Krystal Biotech is seeking a highly motivated Process Validation Associate (1+ years’ experience) or Engineer (3+ years’ experience) to support process validation planning, design, and execution. This person will be responsible for risk assessments, process improvements, investigations, and other projects. They will also play a pivotal role in technology transfer and ensuring processes transition properly from site to site. | 7/5/2023 |
| 4458 | Krystal Biotech Pittsburgh, PA Manufacturing Sciences & Technology (MSAT) Associate Bachelor’s degree. Exp: 1+ year |
Krystal Biotech, Inc is seeking a highly motivated Manufacturing Sciences and Technology (MSAT) Associate to support technical transfer and continuous improvement of product manufacturing at our growing GMP facility. The Associate will have a critical role and operate cross-functionally in the development of our products and processes across a range of manufacturing activities. | 7/5/2023 |
| 4459 | Krystal Biotech Pittsburgh, PA Quality Control Analyst I/II Bachelor’s degree in life science required Exp: 1+ years |
Krystal Biotech, Inc is seeking a highly motivated and detail-oriented Quality Control Analyst who will perform various assays and analytical testing for the release of drug products, for clinical and commercial use. A strong foundation in cell culture techniques will be essential to this role supporting the development, manufacturing, and release of gene therapy products. | 7/5/2023 |
| 4460 | Krystal Biotech Pittsburgh, PA Regulatory Affairs Associate Bachelor’s degree in a Scientific or related field. Exp: 1-3 years |
Krystal Biotech, Inc is seeking a highly motivated Regulatory Affairs Associate to support all regulatory activities from product development and pre-clinical through product approvals. They will play an active role in preparation of regulatory documents and ensuring submissions are quality in nature and on-time. The Associate will work onsite with the team, based in our Pittsburgh facility. | 7/5/2023 |
| 4461 | KSQ Therapeutics Lexington, MA Associate Scientist/Senior Associate Scientist, In Vivo Pharmacology BSc Exp: 1-2+ yrs |
KSQ Therapeutics is seeking an Associate Scientist/Senior Associate Scientist with an interest in discovering and advancing the next generation of cell therapies for the treatment of cancer to join the in vivo pharmacology team. Our ideal candidate thrives in a research environment that demands teamwork, scientific rigor and technical excellence. Previous hands-on in vivo experience is required. Interested people with experience in the discovery and development of NK/T cell adoptive cell therapies are strongly encouraged to apply. The ideal candidate would be able to learn additional in vivo and ex vivo activities as needed to support the progression of our immuno-oncology pipeline and engaging partnerships. They will work as part of a team to ensure delivery of key data sets as well as develop and deliver scientific presentations and reports. | 7/5/2023 |
| 4462 | LakePharma Rensselaer, NY Process Engineer I Bachelor’s degree in Biology, Chemical Engineering or related field Exp: 0-3 years’ |
The Process Engineer I will be responsible for facilitating the tech transfer of client processes and executing engineering functions including design, scale up document controls. | 7/6/2023 |
| 4463 | LakePharma Rensselaer, NY Production Technician Associates or Bachelor's degree preferred. Exp: 0+ years |
The Production Technician is an integral part of the team, contributing to our success by weighing out chemicals and preparing various types of solutions for use in process. | 7/6/2023 |
| 4464 | LakePharma Lebanon, NJ Microbiology Lab Analyst I BS in Microbiology or a related scientific discipline or MS in Microbiology or a related scientific discipline. Exp: BS: 0-2 years ; MS: 0 years |
The Microbiology Laboratory Analyst I is an integral part of the Curia team, contributing to our success by assisting in the execution and development of technical and business aspects of the Microbiology Laboratory. As the Microbiology Laboratory Analyst I you may be responsible for sample intake, performing sample analyses, and any other tasks as assigned by management. Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients’ lives with the pharmaceuticals we develop and manufacture. | 7/6/2023 |
| 4465 | LakePharma Albany, NY Research Scientist I; Medicinal Chemistry Bachelors or Masters Degree with major in chemistry. Exp: 0-5 years |
The Research Scientist I is an integral part of the Curia team, contributing to our success by the synthesis, purification and identification of intermediates and target compounds. The Research Scientist I is expected to demonstrate expertise in both the theoretical and practical aspects of organic chemistry. Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients’ lives with the pharmaceuticals we develop and manufacture. | 7/6/2023 |
| 4466 | Liquidia Morrisville, NC Manufacturing Technician B.S. degree Exp: 0-2 year’s |
We are looking for a hands-on and experienced Manufacturing Technician. In this role, you will perform routine running of manufacturing equipment to support production and R&D efforts. Furthermore, you will provide feedback to engineering and scientific staff on process performance and ideas for process improvement. | 7/7/2023 |
| 4467 | Liquidia Morrisville, NC Associate Scientist, Quality Control Lab B.S. degree in chemistry, pharmaceutical sciences, or a similar scientific field. Exp: 0-2 years’ |
We are looking for an Associate Scientist, Quality Control Lab, located at our headquarters office. In this “hands-on” role within the Quality Control Lab, the Associate Scientist will join a talented and collaborative team that welcomes input and suggestions to help continue Liquidia’s upward trajectory at the most exciting time in the Company’s history. Critical to success are a scientific laboratory background, ability to follow CGMP documentation requirements, and excellent communication skills. The Associate Scientist will conduct laboratory analysis of raw materials and intermediates in support of Liquidia’s lead product candidate, for PH. | 7/7/2023 |
| 4468 | Lyra Therapeutics Watertown, MA MSAT Engineer I/II Bachelor’s Degree (Engineering Preferred) Exp: 1+ years |
Our team is growing, and we are currently recruiting a Manufacturing Sciences and Technology (MSAT) Engineer I/II to support pharmaceutical operations at the Waltham and Watertown, MA sites. The focus of this position is to ensure manufacturing equipment and processes are operating as intended to meet the requirements for drug product manufacturing. This position will play a key role in delivering results in a fast paced, highly collaborative, and dynamic environment. The position will assist in the startup of a combination drug-device product from new product launch through commercial production. This involves process development, commercial process validations, technology transfers, as well as being accountable for commercial production. | 7/7/2023 |
| 4469 | Mammoth Biosciences Brisbane, CA Research Associate I/II, Tx Platform Development Bachelor’s degree in molecular and cell biology, immunology, biochemistry, or a related field. Exp: 1 year |
Mammoth is hiring a Research Associate I/II to contribute to R&D projects run within the Platform team. The Platform team develops next-generation CRISPR tools for therapeutic genome editing applications and is composed of technical staff with diverse strengths in bioinformatics, biochemistry, protein engineering and high-throughput screening. The successful candidate will work on CRISPR tool development projects during their early (proof-of-concept) and/or late (optimization) phases. This is a fantastic opportunity to impact human health by making CRISPR tools that cure genetic disease. | 7/7/2023 |
| 4470 | Mammoth Biosciences Brisbane, CA Research Associate I/II/Senior Research Associate- Screening and Assay Development Bachelor’s or Master's degree in molecular biology, genome sciences, biochemistry, or a related field. Exp: 1 year |
Mammoth is currently seeking a creative and detail-oriented Research Associate with interest in translating CRISPR research into the clinic. The ideal candidate will join the assay development team to work collaboratively to execute essential workflows that support efficacy validation for many preclinical programs. The ideal candidate will be part of the screening and assay development team, which is responsible for measuring DNA, RNA, and protein from tissues and cells. These activities include measuring CRISPR induced editing events in DNA, digital PCR to measure guide and mRNA stability and distribution, and western blots and ELISAs to measure protein quantity and stability. Additionally, supports high throughput screening of CRISPR systems for different cell model systems. | 7/7/2023 |
| 4471 | Masy BioServices St. Louis, MO Associate Scientist I, Chemistry Bachelor’s degree in Pharmaceutical Sciences, Chemistry or equivalent required. Exp: 1+ years |
The Associate Scientist I is accountable for driving results in a fast-paced environment by performing analytical routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. For this position, HPLC, dissolution and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company). The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 7/7/2023 |
| 4472 | Masy BioServices St. Louis, MO Associate Scientist I, Microbiology Bachelor’s degree Biology, Microbiology or related field. Exp: 0-2 years |
The Associate Scientist, Microbiology is accountable for driving results in a fast-paced environment by accurately and efficiently performing sample analysis, monitoring microbial cultures and identifying microbiological contaminants and pathogens using a variety of identification methods. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 7/7/2023 |
| 4473 | Masy BioServices Wilmington, NC Associate Scientist I/II Bachelor’s degree in Chemistry or related field. Exp: 0 – 4+ years |
The Associate Scientist I or II is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of active pharmaceutical ingredients development or pharmaceutical manufacturing. This position may also be required to work on method development/method validation projects. Typical types of testing include: assays (potencies, related substances, residual solvents, metals etc.), moisture content, identification, and various other wet chemistry based measurements. HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations, UV, DSC, TGA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client/vendor supplied or developed by Alcami). The Associate Scientist II must have the ability to efficiently organize the routine work with minimum supervision and to properly evaluate and interpret generated data is required. The Associate Scientist II will occasionally be called upon to support and mentor other Analytical Chemists within the lab. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 7/7/2023 |
| 4474 | Masy BioServices Wilmington, NC Associate Scientist III - QC Testing Master’s degree in Chemistry or a related field. Exp: 0-5 years |
The Associate Scientist III is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Associate Scientist may also assist with method development/method validation projects. For this position, HPLC, dissolution and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: CKF/KF, ICP-MS, Particle Size, CCIT, UV. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 7/7/2023 |
| 4475 | Masy BioServices Morrisville, NC Associate Scientist II - Raw Materials Bachelor's degree in Pharmaceutical Sciences or Chemistry or Master's degree. Exp: BS: 1 years; MS: 0 years |
The position is responsible for support of compendial testing group and manages priorities of this team to provide the timely, compliant and accurate testing of raw materials, critical utilities, in-process samples and finished product. This position will collaborate with cross-functional teams and will work side-by-side with other scientists and professionals to drive the scientific agenda. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 7/7/2023 |
| 4476 | Mekonos Berkeley, CA Research Associate, Microfluidics B.S or M.S in a relevant engineering or scientific discipline Exp: 0+ years |
We are looking for a Microfluidics Research Associate to join us and have an impact in the following ways: Design, build and test microfluidic parts Plan and execute research operations Demonstrate high scientific integrity and reporting standards Promote a positive and exciting work environment This is an in-person role, based in Alameda, CA. You are not expected to have experience with all listed requirements. If you feel passionately about our mission and values, please consider applying. | 7/7/2023 |
| 4477 | Myriad Genetics Salt Lake City, UT Lab Tech I (myRisk Post Lab, Nights Sun-Wed 8p-6:30a) Bachelor’s degree in a chemical, physical, biological or clinical laboratory/medical technology science. Exp: 1+ years |
Responsibilities Complying with the laboratory’s technical, administrative and safety policies and procedures. Participating in the laboratory’s quality assurance plan, adhering to quality control and preventive maintenance policies and appropriately documenting these activities. Working as part of a team to produce repeatable quality results. Maintaining a clean and organized laboratory space. Following Standard Operating Procedures (SOPs). Operating high performance liquid handling robots. Participating in continuing education according to accepted laboratory standards. Actively participating in successful and timely completion of training and competency assessment as outlined in the laboratory and departmental training programs. | 7/7/2023 |
| 4478 | Myriad Genetics Salt Lake City, UT Lab Tech I (myRisk Post PCR, Weekend Nights Thurs-Sat 6pm-6:30am) Bachelor’s degree in a chemical, physical, biological or clinical laboratory/medical technology science. Exp: 1+ years |
Myriad Genetics is looking for a Lab Tech to join our myRisk PCR Post Lab Team. MyRisk with RiskScore® is a powerful tool that evaluates 48 genes to help healthcare providers identify their patients’ risk of developing 11 different types of hereditary cancer. More than a test, MyRisk’s clear, actionable results are the foundation for personalized care plans that can be used to help patients make confident, informed decisions about their medical management. The is a full-time position and the schedule for this position is Thursday through Saturday 6:00pm-6:30am MST. | 7/7/2023 |
| 4479 | Indigo Biosciences State College, PA Associate Scientist Master’s Degree in a relevant field of the biological sciences. Exp: 0+ years |
INDIGO’s Associate Scientists are bench scientists that work within a Research Team. It is expected that they will be intellectually engaged in critically evaluating experimental data, trouble-shooting technical problems, brainstorming the application of new or alternative technologies/methods, and interacting with INDIGO’s Sales and Marketing Teams, as well as directly with our customers. | 6/27/2023 |
| 4480 | Instil Bio Tarzana, CA Technician, QC Analytical Bachelor Degree Exp: 0+ years |
Instil Bio is looking for a highly motivated and driven individual to join us as a technician in the Quality Control organization. Initially as part of the start-up activities, you will be responsible for establishment and set-up of the QC testing laboratories in Tarzana area. As the site transitions into operation, you will primarily be responsible for providing technical expertise, testing and release of product, package material, raw material used in the production of Instil Bio’s cell therapy product. | 6/27/2023 |
| 4481 | Pace Analytical Maplewood, MN Lab Analyst - Rheology B.S. in Chemistry, Physics, Materials Science, Engineering or related field. Exp: 0+ years |
Join us as a Lab Technician Rheology, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. A candidate for this position should be familiar with mechanical properties testing including dynamic mechanical analysis (DMA), tensile testing, lap shear, etc. A candidate would be expected to follow standard procedures to prepare samples, set up instrumentation and run experiments and process data. A candidate will report results using previously developed standard formats. | 6/27/2023 |
| 4482 | Pace Analytical Minneapolis, MN GC LC Chemist - Analytical Instrument Specialist BS degree in chemistry or related science. Exp: 0+ years |
Instrument Services Specialists are responsible for providing technical solutions and an advanced level of instrument support services to customers of TFS, including external clients, laboratory chemists within the Pace lab system, and departmental coworkers. They also provide our customers with a variety of support services associated with their analytical instrumentation. These services include routine maintenance, operational and performance testing, hardware and software troubleshooting, instrument repair, and personnel training. | 6/27/2023 |
| 4483 | Pace Analytical Brooklyn Park, MN Microbiologist Bachelor's degree in Microbiology, Biology or a related discipline required. Exp: 1 year - 4 years |
Join us as a Microbiologist, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. The main function of the QC Microbiologist is to perform supportive activities for general lab readiness, conducting critical biological tests, and following SOPs to perform methods using analytical skills and understanding of biological and chemistry techniques and principles. | 6/27/2023 |
| 4484 | Pace Analytical Greenfield, IN Microbiologist/Molecular Biologist Bachelor's degree in Biology, focus in Microbiology and Molecular Biology preferred. Exp: 1+ years |
Candidate will use their skills and knowledge in Microbiology, Molecular Biology and Bacteriology to support development of new products. | 6/27/2023 |
| 4485 | Pace Analytical Maplewood, MN Microbiologist- Food Safety BS degree in Biology, Microbiology, or related science. Exp: 0+ years |
Join us as a Microbiologist, where you’ll put your love of science to work in the Scientific Insourcing Solutions division. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. This position will actively support food safety and quality assurance through the use, and validation of, pathogen detection products. The analyst will prepare and evaluate samples using aseptic technique to ensure products meet specifications. The products being monitored are crucial to maintaining consumer safe food supply chains. Work is performed as part of a team in a collaborative environment. Position may require occasional weekend shifts. | 6/27/2023 |
| 4486 | Pace Analytical Sugar Land, TX Chemical Technician 1 - Entry Level Bachelor's degree in chemistry or biology preferred. Exp: 0-2 years |
Join us as an Entry Level Chemical Technician, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. The main function of a laboratory technician is to conduct chemical and physical laboratory tests to assist scientists in making qualitative and quantitative analyses of solids, liquids, and gaseous materials. The chemical technician will work in an experimental lab on research and development projects including hands on wet bench chemistry, chemicals handling, preparation of solutions/dilutions as well as routine analytical characterization and data analysis. Note: This position is expected to last 1 year. | 6/27/2023 |
| 4487 | Pace Analytical Eagen, MN Scientist (Chemists, Lab Technicians) Bachelor's degree in Biology, Chemistry, Physics, and other related science. Exp: 1+ years |
Join us at Pace, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. This is a lab based position. The candidate will be conducting various physical and chemical tests to assist scientists in making qualitative and quantitative analyses. Role may involve wet bench lab work, chemical handling, preparation of solutions/dilutions as well as routine analytical characterization and data analysis. Various shifts may be available. Several locations within the Minneapolis area and surrounding cities. These positions are contracted positions which may last up to 12 months. Note: This is an evergreen posting for future positions within our team. | 6/27/2023 |
| 4488 | Charles River Laboratories Watertown, MA Research Associate I 1 BS in the biological sciences or a relevant field is required. Exp: 0-3 years |
In the Research Associate role, you have the responsibility of performing a variety of animal procedures to support company and client research projects. This includes setting up study forms, preparing procedure rooms, and labeling and shipping samples. You will also perform various procedures, such as administering drugs through different routes (oral, SC, IP, IM, IV), collecting blood/tissue samples, and performing grafting techniques. In addition to these tasks, you will operate and maintain laboratory equipment (e.g., isoflurane machine). The Research Associate will be responsible for accurate data entry. To ensure the success of the research projects, it is critical that you maintain accurate study records and assist in maintaining lab and facility inventories. As part of your role, you will be expected to complete study reports and perform routine animal health-related tasks such as changing cages or supplying food as needed. Your attention to detail and ability to follow procedures carefully will be essential to ensure the accuracy and reliability of your research results. Lastly, you may need to perform health rounds and treatments on weekends, holidays, and occasional evenings.In the Research Associate role, you have the responsibility of performing a variety of animal procedures to support company and client research projects. This includes setting up study forms, preparing procedure rooms, and labeling and shipping samples. You will also perform various procedures, such as administering drugs through different routes (oral, SC, IP, IM, IV), collecting blood/tissue samples, and performing grafting techniques. In addition to these tasks, you will operate and maintain laboratory equipment (e.g., isoflurane machine). | 6/27/2023 |
| 4489 | Charles River Laboratories Northridge, CA Quality Control Associate AA or BS degree in Life sciences preferred. Exp: 0-2 years |
The QC Associate I supports the Quality Control Manager to maintain the Quality Control program at Cell Solutions Charles River Laboratory, Northridge. The QC Associate will be responsible for performing Quality Control testing of samples/materials generated during the manufacturing of all cryopreserved products, perform microbiological Environmental Monitoring of Cell Processing/Clinical Labs as well as activities covering the inspection, sampling and testing of incoming raw materials. | 6/27/2023 |
| 4490 | Charles River Laboratories Mattawan, MI Research Technician - Second Shift Operations *$1,000 sign on bonus *$20/hr starting wage Bachelor’s/Master’s Exp: 0 years |
We are seeking a Research Technician for our Second Shift Operations at our Safety Assessment site located Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. | 6/27/2023 |
| 4491 | Charles River Laboratories Worcester, MA Research Technician I Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months |
We have an exciting opportunity for a Research Technician 1 (Tuesday - Saturday hours) at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. | 6/27/2023 |
| 4492 | Charles River Laboratories Worcester, MA Research Technician I Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months |
We have an exciting opportunity for a Research Technician I at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. This is a Monday - Friday 2:30-11:00am position.We have an exciting opportunity for a Research Technician I at our Discovery site located in Worcester, MA. | 6/27/2023 |
| 4493 | Charles River Laboratories Mattawan, MI Research Technician I- Molecular Imaging Bachelor’s/Master’s Exp: 0 years |
*$1,000 new hire sign on bonus and $20/hr starting wage Job Summary We are seeking a Research Technician for our Molecular Imaging Team located in Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. | 6/27/2023 |
| 4494 | Charles River Laboratories Mattawan, MI Research Analyst II, Discovery Bioanalytical 1 BS/BA in relevant field. Exp: 1 year |
Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP’s and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents. | 6/27/2023 |
| 4495 | Genesis Therapeutics San Diego, CA (Sr.) DMPK Research associate A Bachelor’s, Master’s or Ph.D. in Chemistry, Biological Sciences, Pharmacology or related discipline. Exp: 1-2+ years |
Genesis Therapeutics is pioneering artificial intelligence guided rational drug design to address severe unmet medical needs for patients. Our lab in San Diego is looking for a motivated and versatile Drug Metabolism and Pharmacokinetics (DMPK) Scientist or Sr Scientist to join our team to help advance our compounds through preclinical and clinical development. The successful candidate will be involved in drug discovery and development through the conduct of DMPK assays. This is a full-time position in a fast-paced biotech environment with a collegial group of high-level colleagues working towards well-defined goals. Full medical and dental benefits, flexible work hours/vacation included in this opportunity to learn all aspects of biotech start-up. | 6/28/2023 |
| 4496 | Integra LifeSciences Mansfield, MA PROJECT ENGINEER, LCM OPERATIONS Master’s degree in mechanical, manufacturing, materials or biomedical engineering. Exp: 1-3 years |
ESSENTIAL DUTIES AND RESPONSIBILITIES: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Lead and Participate on cross-functional project teams including R&D, Quality Assurance, Supplier Quality, Planning, Purchasing, Regulatory, and Manufacturing to maintain and improve surgical products. Develop project plans for qualifications and ensure team resources identified, team members help accountable to deliverables, and milestones met. Provide engineering knowledge and oversight to resolve manufacturing- and quality-related problems with existing products. Support and lead manufacturing process improvements for CSS products in both internal manufacturing facilities and in partnership with external suppliers. Provide project leadership to improve existing products and associated manufacturing processes. | 6/29/2023 |
| 4497 | Integra LifeSciences Boston, MA ENGINEER II, QUALITY Master degree in Quality Assurance, Biological Sciences or discipline. Exp: 0-2 years |
The Quality Engineering team focuses on product compliance in support of Product Design and Manufacturing, including the critical quality system elements of CAPA, Complaint Investigations, Risk Management, Process/Test Method/Equipment Validations, Deviations, Control of Nonconforming Product, Product Holds, Microbiology and Equipment management. Works closely with Operations, Manufacturing Engineering, Design Engineering and Post-Market Surveillance groups to ensure a high level of product quality and effective and efficient investigations when needed. | 6/29/2023 |
| 4498 | Integra LifeSciences Boston, MA ENGINEER II, QUALITY VALIDATION Master degree in Engineering (Biomedical, mechanical, chemical, or electrical) or Science (Biology, Chemistry) Exp: 0-2 years |
Responsibilities associated with this position are directly associated with the introduction and launching of new or products and processes into a manufacturing facility. The candidate must utilize problem solving techniques to resolve issues and conflict in order to meet the high level goals set forth by the organization. The candidate must be well organized and technically sound in understanding scientific rationale and justifying criterion from a quantitative standpoint. The candidate must be familiar with process flow of a medical device organization, including the regulatory impact of change and the documentation path of a compliant process. The candidate must possess technical writing experience in protocol generation and procedure generation. Some experience is required in master plan generation and the change control life cycle. The candidate must be a team player who thrives in a team environment, but also has the capability to work on their own to research and investigate. Gown qualification is a plus, with an understanding of clean room practice and cGMP environments. The qualified candidate must understand the concepts of risk management and the ability to identify and classify critical parameters within a production setting. | 6/29/2023 |
| 4499 | IQVIA Austin, TX Laboratory Associate - Automation Bachelor’s Degree in Chemistry or a related field. Exp: 1 year |
Responsible for routine sample preparation duties inclusive of automated liquid handling, troubleshooting routine experiments and the preparation of solutions. | 6/29/2023 |
| 4500 | IQVIA Santa Fe, NM Research Associate Bachelor’s degree or higher in Biology, Biochemistry, Molecular Biology, or related life science fields Exp: 1+ years |
You will assist our scientific team in empowering Pharma companies to develop new antibody-based therapeutics. We expect you to be enthusiastic, curious, and to have a strong team player attitude. You will be hired as part of the Laboratory Operations Team, which provides support to the entire Specifica Scientific Team. | 6/29/2023 |
| 4501 | IQVIA Durham, NC Scientist, Assay Development Bachelor's Degree in relevant scientific discipline (Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technol Exp: 1 year |
The Scientist for Assay Development contributes to the design of and is responsible for experiment execution of assay/method development. | 6/29/2023 |
| 4502 | IQVIA Ithaca, NY Associate Scientist,Sample Prep (Sign on bonus offered) Bachelor's Degree in a Life Sciences discipline required. Exp: 6 months |
Responsible for routine sample preparation duties inclusive of troubleshooting routine experiments and the preparation of solutions and reagents. | 6/29/2023 |
| 4503 | IQVIA Valencia, CA Laboratory Associate- Microbiology Bachelor's Degree Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree required. Exp: 6 months |
Responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. | 6/29/2023 |
| 4504 | IQVIA Valencia, CA Laboratory Associate- Automated Chemistry Bachelor's Degree. Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree required. Exp: 6 months |
Responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. | 6/29/2023 |
| 4505 | IQVIA Atlanta, GA Laboratory Associate Bachelor's Degree Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree Required. Exp: 6 months |
Shift Tuesday-Saturday 3:00PM-11:00PM Responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. | 6/29/2023 |
| 4506 | MEDTOX Greenfield, IN Research Assistant BS/BA degree in science or related field. Exp: 1+ years |
Performs basic laboratory operations independently with detailed review of results by experienced personnel Incumbent has a basic understanding of the technical area of responsibility. | 6/29/2023 |
| 4507 | MEDTOX Somerset, NJ Research Analyst - BioAnalytics Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1+ years |
Labcorp Drug Development is the leading global Clinical Research Organization. We have an exciting career opportunity for an Research Analyst on our BioAnalytical team in Somerset, NJ. Are you interested in working in the research field? Do you have LCMS experience? Join an organization that truly believes in employees learning and growing a career. The Analyst is focused on the extraction of biological samples (Protein Preciptation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. This position is a day shift with a flexible start time between 6am and 9am. | 6/29/2023 |
| 4508 | MEDTOX Raritan, NJ Technologist Associate’s or Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requir Exp: 1 year |
New Grads Welcome – Full Training Provided Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Medical Technologist or Technician in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. Esoteric Dept. The work schedule for this position will be Mon-Fri 11:30PM - 8:00AM, Rotating weekends | 6/29/2023 |
| 4509 | MEDTOX Raritan, NJ Cytotechnologist Bachelor of Science degree from an accredited college/university. Successful competition of an accredited Cytology program. ASCP Cytotechnologist (CT) Exp: 1 year |
This position includes a $15,000 Sign-On Bonus! (External candidates only) Are you a certified Cytotechnologist? Are you in school pursuing a Cytotechnologist degree/certification? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a full-time Cytotechnologist in Raritan, NJ. This will be a fast paced, customer focused, and challenging environment. LabCorp has a comprehensive benefits package and competitive compensation. LabCorp offers opportunities with advancement potential in an influential and expanding company. Be a part of something where you can make an impact on improving health and improving lives. Schedule: Monday through Friday between the hours of 6:00am and 7:00pm, and every 3rd Saturday | 6/29/2023 |
| 4510 | MEDTOX Raritan, NJ Clinical Laboratory Technologist- Hematology Department Associate’s or Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requir Exp: 1 year |
New Grads Welcome – Full Training Provided Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Medical Technologist or Technician in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. The work schedule for this position will be Monday- Friday, 11:30 PM- 8:00 AM, Alternating Saturday | 6/29/2023 |
| 4511 | MEDTOX Raritan, NJ Clinical Laboratory Technologist - Immunology Associate’s or Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requir Exp: 1 year |
New Grads Welcome – Full Training Provided Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. The work schedule for this position will be 2.00pm to 10.30pm ; Tuesday to Saturday | 6/29/2023 |
| 4512 | MEDTOX Raritan, NJ Clinical Laboratory Technologist - Mass Spectrometry Associate’s or Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requir Exp: 1 year |
Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Medical Technologist or Technician in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. The work schedule for this position will be Tuesday- Saturday, 10:00pm - 6:30am. | 6/29/2023 |
| 4513 | Merck Durham, NC Associate Manufacturing Automation Specialist B.S., B.A., or greater preferably in Engineering, Science, or Information Technology Exp: 1+ years |
The Associate Manufacturing Automation Specialist position shall support the expansion of a GMP testing laboratory at a manufacturing facility for sterile vaccine products. Responsibilities include supporting computer system validation, implementing process control and data collection, and troubleshooting in compliance with SDLC, cGMP, safety, and environmental regulations. The Manufacturing Automation Associate Specialist must actively support, participate, and embrace an empowered team culture including significant interaction with manufacturing, quality, IT, and engineering groups. This role supports a large spectrum of sophisticated automated systems within Laboratory Operations; providing multiple opportunities to learn new automation technologies and make a positive impact. | 6/29/2023 |
| 4514 | Merck West Point, PA Engineering, Maintenance & Utilities 2nd Shift Associate Specialist B.S. Engineering, Science, or four-year Engineering Technology Degree Exp: 1+ years |
Under the supervision of a Senior Specialist or Associate Director, the EMU Associate Specialist is responsible to provide day-to-day equipment and facility engineering support for assigned area including vaccine bulk manufacturing, and/or associated facility/utilities mechanical support. Assigned tasks include support and monitoring of equipment performance and maintenance, propose and develop equipment and facility improvements and troubleshoot process equipment to ensure reliable, compliant and efficient operations. Actively ensures compliance to current Good Manufacturing Practices (GMP), Safety, and Environmental regulations while achieving operating cost goals. | 6/29/2023 |
| 4515 | Merck Rahway, NJ Scientist, Small Molecule Analytical Research & Development Master of Science degree in Chemistry, Pharmaceutical Sciences, or related fields. Exp: 0 years |
The Small Molecule Analytical Research and Development group has an opening for a Scientist based in Rahway, NJ. Join us and experience our culture first-hand - one of strong ethics & integrity, diversified experiences, exceptional science and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. In your role as Scientist, you will be part of a team of Analytical Chemists working on cross-functional scientific teams to enable novel small molecule, peptide, and oligonucleotide drug development through laboratory-based analytical characterization and statistical data analysis. | 6/29/2023 |
| 4516 | Merck Rahway, NJ Process and Data Engineer Bachelors or higher in Mathematics, Statistics, Economics, Business Information Systems, Computer Science/MIS, Finance/Accounting, Engineering, Scienc Exp: 1-4 years |
Our Quantitative Sciences team use big data to analyze the safety and efficacy claims of our potential medical breakthroughs. We review the quality and reliability of clinical studies using deep scientific knowledge, statistical analysis and high-quality data to support decision making in clinical trials. | 6/30/2023 |
| 4517 | Merck Kenilworth & Rahway, NJ Associate Scientist, Sterile & Specialty Products. This Job Is Available In 2 Locations. B.S. degree in Chemical / Biochemical / Biomedical Engineering, Materials Science, Pharmaceutics, Pharmaceutical Chemistry, Pharmaceutical Sciences, C Exp: 1+ years |
We are seeking a motivated engineer / scientist to work collaboratively in a team environment to help solve key challenges in formulation development and manufacturing of parenteral pharmaceutical products. The successful candidate will be a passionate scientist with strong academic fundamentals and a drive to develop new medicines to improve human health. In this role, the individual will be responsible for supporting the formulation development of new biological / chemical entities as part of a matrix team from initial first-in-human formulations to commercialization. The successful candidate must be able to collaborate in a fast-paced, integrated, multidisciplinary team environment. | 6/30/2023 |
| 4518 | Merck West Point, PA Shift Engineer - 3rd Shift, Monday - Friday BS in Engineering or comparable scientific background. Exp: 1 years |
Our Engineers support internal and external manufacturing operations remain operational, continuously improve and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation. Position Description: The function of this position is to provide technical support for vaccine purification facility while actively supporting, participating in, and embracing an empowered culture. This role is for Off-Shift Engineering Support (3rd Shift, Monday through Friday). 3rd shift (12am-9am) | 6/30/2023 |
| 4519 | Stryker Portage, MI Electrical Design Engineer(ENTRY LEVEL) Bachelor's degree in EE or related discipline. Exp: 0-2+ years |
We are currently looking for an Electrical Design Engineer to be responsible for a wide variety of engineering work in support of current production medical devices including design changes, process/quality improvements and compliance issues. You will also support and conduct root cause analysis, verification and validation testing, manufacturing transfer activities and component obsolescence management for existing products. | 6/20/2023 |
| 4520 | Stryker Salt Lake City, UT Manufacturing Engineer Bachelor’s degree in Engineering required. Exp: 1+ years |
Stryker’s Neurovascular Manufacturing division is seeking to hire a Manufacturing Engineer in Salt Lake City, Utah. | 6/20/2023 |
| 4521 | Stryker Portage, MI Mechanical Engineer, R&D – Sustainment Bachelor’s Degree in Mechanical Engineering Exp: 0+ years |
Stryker is seeking to hire a Mechanical Engineer, R&D to support Medical’s Acute Care Product Engineering team. This role is hybrid, in Portage, MI with the expectation to come into the office a minimum of 3 days a week. | 6/20/2023 |
| 4522 | Acrotech Biopharma East Windsor, NJ CHEMIST A BS/MS in a Scientific field. Exp: 1-3 years’ |
The Chemist will perform a variety of testing to assess the strength, identity and purity of finished product, which are mainly oral solids and/or raw materials. The Chemist will work as a member of a team to effectively plan and develop/validate new methods (for Assay, Dissolution, Residual solvents, and Related compounds tests) to execute analytical testing and/or test using established (official and/or in-house) test procedures. The Chemist may execute 90% - 100% of their work at the bench level. | 6/20/2023 |
| 4523 | Acrotech Biopharma East Windsor, NJ ASSOCIATE, AUTOMATION ENGINEER Masters in Industrial & Systems Engineering or Mechanical Engineering Exp: 1-2 Years |
The role of the Automation Engineer is to perform as-is study of current process and provide recommendation on Automating and de-skilling current manual process. Associate should be willing to learn and work on ERP, Warehouse Control System, PLC , HMI and has logical approach towards trouble shooting a problem The position works closely with Automation & Project Management team, on the new requirements and enhancements and takes up continuous improvement projects to drive the operational efficiencies across the Distribution Center | 6/20/2023 |
| 4524 | Meridian Bioscience Memphis, TN Lab Production Associate Bachelor’s or Master’s degree from an accredited institution with a relevant scientific discipline such as Chemistry, Biology, Biochemistry, Molecular Exp: 1+ years |
The Lab Production Associate position is responsible for performing assigned manufacturing and laboratory support activities according to company policies, SOPs, and quality regulations. The position will be responsible for performing upstream and downstream bioprocessing procedures to support the commercial manufacturing of native antigens, recombinant proteins, antibodies, and blockers. Upstream processes include tissue culture, cell bioreactors, fermentation, virus propagation, cell and virus bank production, and buffer/media preparation. Downstream unit operations include harvest, clarification, chromatography, centrifugation, TFF (UF/DF), filtration, formulation, and fill-finish. The candidate will be required to maintain an assigned lab area and perform equipment and lab cleaning procedures. The candidate must be able to execute assigned procedures in a fast-paced and results-oriented environment satisfying quality standards in accordance with customer satisfaction, cost, schedule, and ISO1345 regulations. | 6/20/2023 |
| 4525 | Repligen Waltham, MA ELISA Manufacturing Associate I - 2nd shift AS/BS in biotechnoloy related study. Exp: 0-2 years |
This position will function in Repligen’s ELISA group. The successful candidate will play a key role in ensuring that the ELISA department's production and quality goals are met. The individual must be able to follow oral and written instructions accurately and complete tasks in a timely manner. Experience working in a GMP/ISO/document-controlled environment would be beneficial. Attention to detail and the ability to work independently and in a team environment are essential. Candidates must be willing and able to learn new manufacturing processes as the company grows. This position will support the 2nd shift. | 6/20/2023 |
| 4526 | Cosette Pharmaceuticals South Plainfield, NJ Research Scientist I Master’s degree in chemistry or pharmacy. Exp: 1-2 years |
The Research Scientist I will be responsible for: • Analytical method Development and Validation • Development and Validation of In vitro methods for Complex generic dosage forms • Maintain full compliance with US FDA – cGMP regulations. • Resolve technical problems and participate in troubleshooting when required | 6/22/2023 |
| 4527 | Delfi Diagnostics Palo Alto, CA Clinical Laboratory Associate, Contractor (Tues-Sat) BS in Biomedical Laboratory Sciences, Clinical Science, or equivalent. Exp: 1+ years |
In this role, you will be responsible for the pre-analytical phase of testing (e.g., specimen receipt, accessioning, and plasma/buffy coat isolation) and assisting with general laboratory operations, such as equipment maintenance, labware cleaning, and reagent manufacturing. | 6/22/2023 |
| 4528 | DiabetOmics Hillsboro, OR Research Assistant/Associate in Product Development (2 positions available immediately) BA/BS in a relevant biological science. Exp: 1-2 years |
Applies knowledge of scientific principles and concepts to the design, development, and execution of Product Development experiments. Demonstrates technical proficiency, scientific creativity, collaboration with others and can work independently. Under guidance of senior personnel, designs and conducts research and/or product development, assay optimization and scale-up tasks and experiments based on the needs of the group. Ensures compliance with and helps to implement the requirements of working in a regulated environment to assure adherence to various requirements, including Design Control, Good Laboratory Practices (GLP), and Good Manufacturing Practices (GMP). Helps to coordinate general laboratory tasks such as reagent preparation, inventory and organization of work. | 6/22/2023 |
| 4529 | Dicerna Pharmaceuticals Lexington, MA Research Associate - Chemistry Bachelors or Masters in Chemistry or related field. Exp: 1-3 years |
Dicerna Pharmaceuticals is seeking a highly motivated Research Associate with a strong background in synthetic and medicinal chemistry to join the Chemistry Team. The candidate will be responsible for the synthesis of oligonucleotide conjugates, nucleoside analogues, small molecule ligands, and linkers. This position will contribute to the development of novel nucleic acid conjugate platforms and support therapeutic programs in multiple disease areas. The Dicerna research team will provide an exciting learning opportunity and a collaborative and fast-paced research environment. | 6/22/2023 |
| 4530 | DxTerity Rancho Dominguez, CA Laboratory Technician/Scientist Molecular Biology, Lab Operations S. or M.S. in chemical, biological or clinical laboratory science, or medical technology from an accredited institution. Exp: 1-3 years |
Testing biological specimens in molecular biology laboratory environment, including high throughput workflows, analyzing the results, and preparing them for reporting. | 6/22/2023 |
| 4531 | DxTerity Rancho Dominguez, CA Research Associate B.S. or M.S Degree in Biochemistry, Molecular Biology or a related field. Exp: 1-3 years |
DxTerity, a patient-centric genomics company located in Los Angeles, CA is looking to hire a Research Associate to join our Research and Product Development team. Responsibilities include: development of molecular diagnostic test kits, reagents and procedures in a team environment. Perform experiments independently after receiving general direction from supervisor. Make detailed observations, analyzes data and interpret results. Prepare technical reports, summaries, protocols and quantitative analyses. Maintain and develop skills in molecular biology and company technology through reading of internal reports and scientific literature. Support the achievement of project objectives and time schedules while meeting ISO and FDA regulatory and design control requirements. | 6/22/2023 |
| 4532 | Ensoma Boston, MA Associate Scientist, Genomics Master’s Degree in a biological science. Exp: one year |
We are seeking an energetic and highly motivated Associate Scientist to join our Platform team. In this role, you will execute standard molecular biology workflows and work collaboratively between groups across the company andperform various next generation sequencing (NGS) assays to characterize and assess therapeutic efficacy and safety. You will partner with top-notch scientists and have an opportunity for accelerated technical skill development and diverse growth and learning opportunities. Do you have a passion for pioneering therapeutics technology development utilizing a broad spectrum of gene editing and modification tools? Are you a great team player, enthusiastic and do you enjoy working in an innovative, collaborative, and fast-paced environment? Join us and be part of a company moving novel gene therapies into the clinic, revolutionizing the reach and access of the curative power of genomic medicines for patients with serious diseases. | 6/22/2023 |
| 4533 | Exagen Diagnostics Vista, CA Laboratory Technician Bachelor’s degree or college courses in Science. Exp: 1+ years |
Responsible for general laboratory task such as buffer preparation and operation of appropriate laboratory equipment. Take direction from and works in collaboration with Technologist in Flow cytometry department. | 6/22/2023 |
| 4534 | Flexion Therapeutics San Diego, CA QA Associate 1 BS/BA degree in scientific discipline from an accredited college or university. Exp: 1 year |
This person is to assist and support the organization with GMP compliance, monitoring conformance to established quality assurance processes and GMP standards for manufacturing. | 6/22/2023 |
| 4535 | Fluxergy Irvine, CA Process Engineer Engineering Degree Exp: 0-2 Years |
As the process engineer at Fluxergy, you will be directly involved in the company’s production activities, as well as deeply involved with the company’s long-term strategy. You will be responsible for process ownership while working with a small but passionate team. This position requires a deep, in-depth knowledge of manufacturing processes, stability and process control. | 6/23/2023 |
| 4536 | Foghorn Therapeutics Cambridge, MA Research Associate - Biochemistry & Biophysics BA/BS in Biochemistry, Biophysics, or related field. Exp: 1+ year |
Foghorn is seeking a highly motivated, enthusiastic, and collaborative Research Associate to join our Drug Discovery team in a lab-based role to support early discovery projects in oncology. As a member of our Drug Discovery team the candidate will have an opportunity to employ various biochemical and biophysical assay technologies in mechanism of action studies, screening and hit validation. This is an onsite and lab based role. | 6/23/2023 |
| 4537 | Frontida BioPharm Vandalia, OH QA Technician I or II (2nd Shift) Bachelor’s Degree required preferably in a related field (i.e., pharmaceutical sciences, chemistry, biology). Exp: 0 - 5 years' |
The QA Technician is responsible for providing quality support to the manufacturing floor, auditing batch production documentation, dispositioning intermediates, performing in process checks, identifying and logging incident reports, and ensuring adherence to cGMP. | 6/23/2023 |
| 4538 | Frontida BioPharm Vandalia, OH QC Chemist I (3rd Shift) Bachelor’s degree in Chemistry or closely related field. Exp: 0-2 years' |
The QC Chemist I is an essential part of the lab Quality team and will be expected to perform physical and chemical testing of intermediate and finished products according to written procedures. | 6/23/2023 |
| 4539 | Frontida BioPharm Vandalia, OH Formulation Technician Bachelor’s Degree in a scientific or engineering discipline preferred. Exp: 1+ years’ |
The Formulation Technician will report to the Associate Director of Formulations and will assist the R&D Formulations staff with product development activities from small scale to commercial batch production. The Formulation Technician should be someone with a keen interest in life sciences or drug manufacturing. This is a developmental role where training is provided, offering an opportunity to learn various techniques of drug manufacturing including dispensing, blending, granulation, compression and coating. | 6/23/2023 |
| 4540 | Fujifilm Diosynth College Station, TX Manufacturing - Associate Process Engineer Bachelor’s degree in Science, Engineering, or other related field. Exp: 1 year |
The Manufacturing Associate Process Engineer is an integral part of the Manufacturing Technical Operations department in College Station, Texas. This position will report directly to the Manager of Technical Operations. Works independently and with colleagues to provide expertise and assistance for the design, development, standardization, and maintenance of an operational biotechnology utilized to manufacture various proteins and other drug substances. This person would provide manufacturing technical support on core manufacturing and operational technologies for the manufacturing unit. Operational biotechnologies include 1. USP: Isolators and biosafety cabinets and their use in cell propagation, Cell Culture/Single Use Technology for adherent and suspension culture; 2. DSP: Dispensing and Mixing and Buffer Preparation, Chromatography, Tangential Flow Filtration, various filtration technologies, centrifugation, and Bulk Fill. This position will also create training programs and perform training for manufacturing technicians in the unit operation categories. | 6/23/2023 |
| 4541 | Fujifilm Diosynth College Station, TX Process Sciences - Associate Engineer Bachelor’s Degree Exp: 1 years |
The Process Sciences - Associate Scientist/Engineer, under general direction, functions within a team based organization to actively address cGMP manufacturing issues. The individual is responsible for analyzing process technologies to assist in the technical transfer of new processes into the manufacturing group. This individual must work in a collaborative manner to assist the transfer of biological drug processes from process development (internal or client) groups in a CDMO environment. | 6/23/2023 |
| 4542 | Fujifilm Diosynth College Station, TX Quality Control - Microbiology Analyst I Bachelor of Science or Associate of Science degree preferably in Biochemistry, Chemistry, Biology or related field. Exp: 0+ years |
The Microbiology Analyst I will be responsible for assisting the QC microbiological aspects of cGMP compliance and testing at the FujiFilm Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory. | 6/23/2023 |
| 4543 | Fujifilm Diosynth College Station, TX QA Analyst I Bachelor’s degree in a related science concentration. Exp: 1+ years |
The Quality Assurance (QA) Analyst I, under direct supervision, will be responsible for assisting with the review and/or approval of basic and technical documentation; Drafting and reviewing of internal Quality policies and procedures; Assisting with product related activities; Assisting with Quality audit functions; Identifying process and Quality System improvements; | 6/23/2023 |
| 4544 | Fujifilm Diosynth Holly Springs, NC Manufacturing Associate II/III *Multiple Positions* MA III: BA/BS Degree in Life Sciences or Engineering. Exp: 0+ years |
The Drug Substance Manufacturing Associate during the project phase is responsible for activities associated with factory acceptance testing (FAT), commissioning, qualification, and validation (CQV) of drug substance process equipment. During the project phase, and as CQV activities allow, create and/or review of manufacturing work instruction or procedures or other manufacturing operational readiness tasks will be required. Travel will be required. At project completion, the associate would transition into manufacturing operations as a manufacturing associate in Drug Substance Manufacturing (DSM) Cell Culture or Purification areas requiring shift work (nights and weekends). | 6/23/2023 |
| 4545 | Fujifilm Diosynth College Station, TX Manufacturing Technician III Bachelor’s degree in Biology, Microbiology, Chemistry, Biochemistry, Engineering, or other related field. Exp: one (1) year |
The Manufacturing Technician III will work directly with a range of technologies. Dependent upon assignment. | 6/23/2023 |
| 4546 | GenMark Diagnostics Seattle, WA Laboratory Assistant I Bachelor’s degree focused in Biology, Biotechnology, Biochemistry, Chemistry, Physics or Engineering field preferred. Exp: 1+ years |
We are seeking driven, self-motivated, and passionate individuals looking to start a career in a fast-paced lab. The position will play an integral role in day-to-day operations as we develop our novel DNA sequencing technology. This position will be based at Roche Diagnostics Seattle, formerly Stratos Genomics. A cover letter is required to be considered for this role. In the cover letter, please be sure to explain how you will meet the below requirements as well as address the following: the technology that Roche Diagnostics Seattle (formerly Stratos Genomics) is developing, why you want to work here, and how you would contribute. | 6/23/2023 |
| 4547 | GenMark Diagnostics Seattle, WA Laboratory Assistant I Bachelor’s degree focused in Biology, Biotechnology, Biochemistry, Chemistry, Physics or Engineering field preferred. Exp: 1+ years |
We are seeking driven, self-motivated, and passionate individuals looking to start a career in a fast-paced lab. The position will play an integral role in day-to-day operations as we develop our novel DNA sequencing technology. This position will be based at Roche Diagnostics Seattle, formerly Stratos Genomics. A cover letter is required to be considered for this role. In the cover letter, please be sure to explain how you will meet the below requirements as well as address the following: the technology that Roche Diagnostics Seattle (formerly Stratos Genomics) is developing, why you want to work here, and how you would contribute. | 6/23/2023 |
| 4548 | GenMark Diagnostics Seattle, WA Lab Assistant II - SBX Nanopore Technology Bachelor’s degree in Molecular biology, Protein Engineering, Bioengineering, Biochemistry or related field. Exp: 1 year |
Roche Diagnostics acquired Stratos Genomics (SBX Nanopore Sequencing) in 2020 for its novel Sequencing by eXpansion (SBX™) technology. SBX™ uses unique applications from chemistry, biochemistry, electrochemistry, and protein engineering to sequence DNA by nanopore in rapid time with high accuracy and low cost. The Sequencing team is devoted to developing our high throughput, low-cost DNA sequencing approach into an industry disrupting product that will facilitate the care that patients need. | 6/23/2023 |
| 4549 | Gritstone Oncology Pleasanton, CA RESEARCH ASSOCIATE I, PROCESS DEVELOPMENT (CONTRACT) Bachelor’s degree (or equivalent) in a scientific discipline or a health-related field. Exp: 0 to 2+ years |
We are looking for an enthusiastic and flexible team player who will thrive in a fast-paced, dynamic, and highly collaborative environment. This individual will work in Process Development Group and contribute to the development of novel adenovirus vaccines and their transfer to manufacturing. | 6/23/2023 |
| 4550 | Haemonetics Boston, MA Reagent Chemist In-Vitro Diagnostics MS in a relevant discipline such as Chemistry, Biochemistry, Biology, Biomedical Engineering, Chemical Engineering, or equivalent. Exp: 0+ years |
Reagent Chemist In-vitro Diagnostics Research & Development Hemostasis Management Hospital Division Boston, MA The Reagent Chemist works alongside a multidisciplinary development project team, responsible for ensuring that the in-vitro diagnostic system, under development, meets its intended goals. The person in this role will develop, optimize and validate reagents for an in-vitro diagnostic system. This role will have technical responsibility for performing testing of raw materials and in-process reagents to support development and transfer to the manufacturing process. | 6/23/2023 |
| 4551 | HistoTox Labs Rockville, MD Laboratory Technician I A Bachelor’s degree in a scientific discipline (i.e., biological sciences, Chemistry, etc.). Exp: 0+ years |
Seeking a Laboratory Technician for our Rockville, MD site. | 6/23/2023 |
| 4552 | HistoTox Labs Rockville, MD Associate Scientist Bachelor’s degree in a scientific discipline (i.e., Biology, Chemistry, Biochemistry, etc.). Exp: 1+ years |
Seeking an Associate Scientist I (In Vitro Cytogenetics). | 6/23/2023 |
| 4553 | HistoTox Labs Madison, WI Upstream Biomanufacturing Laboratory Support Technician Bachelor of Biological Sciences a plus. Exp: 1+ years |
The Laboratory Technician, Upstream Biomanufacturing and Quality Control Testing, will be a member of the lab service’s in vitro biomanufacturing team. The position involves culturing, customer provided, hybridoma cells that produce monoclonal antibodies. Once produced the antibodies are refined, quality control tested, and the finished product is delivered. The company is well established and growing, with a worldwide customer base. Your exciting new career will be cultivated in an environment of continuous improvement. | 6/23/2023 |
| 4554 | Ifyber Ithaca, NY Laboratory Technician BS degree Exp: 1 year + |
The Laboratory Technician will execute on experimental plans at the interface between chemistry, biology, and materials science and support a variety of programs that will require experience and/or the ability to follow detailed protocols, learn and execute bench skills, and adhere to applicable regulatory requirements. | 6/23/2023 |
| 4555 | IGM Biosciences Mountain View, CA Research Associate I / II, Downstream Process Development BS degree in chemical / biochemical engineering, biochemistry, or related field. Exp: RA I: BS with 0+ years; RA II: MS with 0+ years. |
As a Research Associate with experience in process development particularly in the context of antibody and antibody-like biologics. The ideal candidate will have a solid background in protein purification and bioanalytical techniques used to characterize biologics. This is a key position in Process Development and Manufacturing and will have the opportunity to collaborate across groups to contribute to multiple fast-moving drug discovery projects. You will report to a Senior Scientist. | 6/23/2023 |
| 4556 | Imperative Care Campbell, CA Process Development Engineer Bachelor/Master’s in Engineering or related discipline. Exp: less than 2 years |
The Process Development (PD) Engineer I will learn about and assist in product development projects defining, characterizing, optimizing, and validating stable, robust, and capable processes for neuro-interventional medical devices. They will assist in the improvement of internal equipment and processes. Responsibilities will include creative problem solving, critical thinking, application of engineering principles performing process characterization studies, collecting, and analyzing data, and documenting equipment/processes. | 6/23/2023 |
| 4557 | Imperative Care Campbell, CA Preclinical R&D Engineer, II Bachelor's degree in Engineering: mechanical, biomedical, or related discipline, or a Master's degree. Exp: BS: 1+ years ; MS: 0+ years |
What You’ll Do – in this role as a Preclinical R&D Engineer, II, you will have the unique opportunity to work in a small, dynamic team environment advancing the standard of care for stroke treatment through preclinical research and development, anatomical modeling and physician evaluations while working with new product development and commercial teams. This role will be responsible for designing and managing all aspects of physician evaluations, in-vitro bench and simulated use testing, and in-vivo studies, and will partner with Marketing representatives to create marketing collateral via bench and in-vitro testing. | 6/23/2023 |
| 4558 | InBios International Seattle, WA Manufacturing Associate I- ELISA Bachelor’s degree with emphasis on life science. Exp: 1-year |
We are searching for entry-level candidates to join our Biotech manufacturing team to support efforts in producing EUA-approved Covid-19 antigen tests and other InBios products. This position is ideal for someone who wants to start out working in a biotech laboratory/manufacturing environment, learn industry standard good manufacturing practices (GMP), is ready to learn new skills and procedures and is comfortable working with machines and with your hands. We would like to see your resume if you have general industrial or academic laboratory experience and a willingness to learn more lab skills. This position provides opportunity for working with a team and independently on a variety of tasks including preparing buffers, running semi-automated machines, and producing large-scale ELISA diagnostic test components in a BSL-2 laboratory. If you are seeking an entry-level, full-time, on-site position where you can gain experience and grow at the forefront of medical diagnostic biotechnology, this is a great opportunity for you. | 6/23/2023 |
| 4559 | BroadPharm San Diego, CA QC Chemist Bachelor or MS degree in Analytical Chemistry or Organic Chemistry is required. Exp: 1-4 years |
BroadPharm is a fast-growing biotech company which specializes in providing high purity PEG products and customer services worldwide. We are seeking a highly motivated QC Chemist to join our expanding team. The ideal candidate would already have 1+ year of working experience with HPLC, MS, and NMR. The position will work closely with the production team and regulatory manager in addition to the current QC staff. | 6/13/2023 |
| 4560 | Cabaletta Bio Philadelphia, PA Research Associate/Sr. Research Associate, Molecular Biology B.S degree in Life Sciences/Engineering or closely related discipline. Exp: 1-3 years |
Reporting to the Scientist, Molecular Biology we are seeking an experienced, motivated detail-oriented, and highly skilled Research Associate/ Sr. Research Associate within our Molecular Biology Team. Under scientific and technical supervision, the individual will primarily be responsible for manufacturing small and large scale LVV gene therapy vectors across various preclinical programs and disease areas. The candidate should be a highly motivated self-starter with well-established organizational skills who is excited to be a part of the biotechnology industry. The position offers potential growth into additional areas such as molecular biology, immunology, and cell therapy. | 6/14/2023 |
| 4561 | Cabaletta Bio Philadelphia, PA Research Associate/Senior Research Associate, Analytical Development Bachelor’s or master’s degree in biology or closely related discipline. Exp: 1-3 years |
Reporting to the Senior Scientist, Analytical Development, this experienced and motivated Research Associate / Senior Research Associate will support activities of routine analytical testing and method development/qualification to advance CARTA and CAART platforms for pre-clinical and clinical programs. | 6/14/2023 |
| 4562 | Capricor Therapeutics Los Angeles, CA Manufacturing Associate I/II Bachelor’s degree in Biomedical Engineering, Biological Sciences or related field. Exp: 1-3 years |
This position is immediately available to join our Manufacturing team to perform cGMP manufacturing to support Capricor’s clinical trials and exosome development. We are seeking an individual with a scientific background, mammalian cell culture and cGMP experience. | 6/14/2023 |
| 4563 | Capricor Therapeutics San Diego, CA Manufacturing Associate I/II Bachelor’s degree in Biomedical Engineering, Biological Sciences or related field. Exp: 1-3 years |
This position is immediately available to join our Manufacturing team to perform cGMP manufacturing to support Capricor’s clinical trials and exosome development. We are seeking an individual with a scientific background, mammalian cell culture and cGMP experience. | 6/14/2023 |
| 4564 | Abiomed Danvers, MA Equipment Design Engineer I Bachelor’s degree in a Engineering, such as Mechanical Engineering, Industrial Engineering, or Mechanical Design. Exp: 1+ years |
The Equipment Design Engineer I will support , design, develop, and improve, tooling and fixtures for new and existing production floor equipment. In this role, you will be required to meet with different teams to determine their design requirements, plan and execute the design of tools/equipment , develop and test prototypes, and work closely with the manufacturing teams to ensure that design specifications are met. This also includes supporting your peers in design and drafting, engineering change control and equipment qualification, validation, and installation activities. This role will also assist in designing and developing equipment with counterparts in our Aachen, Germany facility. | 6/15/2023 |
| 4565 | Abiomed Danvers, MA Supplier Development Engineer I Bachelor's Degree in Engineering, preferably in Mechanical, Plastics or Manufacturing Engineering Exp: 1+ years |
The Supplier Development Engineer I serves as ABIOMED’s primary technical contact with all US based suppliers, leads all product development team’s supplier initiatives, second source critical suppliers, and establishes “Quality at the Source” programs with key partners. This role is a key technical resource for the company’s continued growth, and is a great opportunity for someone to make a difference at one of the fastest-growing medical technology companies, focused on recovering hearts and saving lives. | 6/15/2023 |
| 4566 | Agilent Boulder, CO Research Associate, Analytical Services Bachelor's degree (B. S.) or equivalent in chemistry, related applied sciences field. Exp: 1+ years |
As a Research Associate in the Analytical Services team the candidate will be responsible for performing sample analysis and supporting analytical method validation. | 6/15/2023 |
| 4567 | Amgen Thousand Oaks, CA Associate - Protein Chemistry Bachelor’s degree in Biochemistry, Biophysics, Analytical Chemistry or related field. Exp: 1+ years |
Let’s do this. Let’s change the world. We are seeking a skilled biochemist to join the Protein Chemistry group within the Protein Engineering Division of Therapeutic Discovery. The Protein Chemistry group is primarily responsible for the optimization, production, assessment, and selection of novel and complex scaffold molecules, often antibody-based, that will be the next generation of large molecules therapeutics. In this vital role you will be a part of a multidisciplinary team with capabilities in protein purification and characterization of large molecule drug candidates. You should be able to interpret and report scientific results that support the generation of publications, patents, or regulatory submissions, and participate in internal and external scientific meetings. Good written and oral presentation skills are a must | 6/15/2023 |
| 4568 | AstraZeneca Gaithersburg, MD 80109216 Associate Scientist - Purification Process Sciences Bachelor's or Master's Degree in Biochemistry, Chemical Engineering, or related field. Exp: 0+ years |
In this role, the Associate Scientist will need to develop and characterize downstream processes for the manufacture of biopharmaceuticals (monoclonal antibodies and other proteins) in late stage clinical development through commercial launch. He / She will be responsible for a portion of a purification development project which will require the scientist to make observations, analyze data and interpret results. | 6/15/2023 |
| 4569 | Bristol-Myers Squibb Redwood City, CA Associate Scientist, In Vivo Pharmacology, Tumor Microenvironment Research Master’s Exp: 0-3+ years |
You will design, plan, and execute in vivo studies, analyze, and present data. You will gain and provide technical and scientific in vivo pharmacology expertise to advance drug discovery programs from target identification/validation to IND enabling activities. You will interact and collaborate effectively in a multi-functional dynamic team environment. | 6/15/2023 |
| 4570 | Bristol-Myers Squibb Devens, MA Associate Scientist/Engineer, MS&T MS in Chemical/Biochemical Engineering or related field. Exp: 0–4 years |
The Associate Scientist, Downstream position in Manufacturing Technology supports the commercial manufacturing of biopharmaceuticals in purification and primary recovery. This position offers the opportunity to provide highly visible technical leadership to resolve complex problems while meeting quality, schedule, and cost objectives. The successful candidate will be a key contributor in a dynamic and highly collaborative team environment. The candidate will set appropriate objectives and priorities, overcome obstacles; and deliver results within project timelines. Expertise and experience in the design, control, and operation of protein purification steps like - chromatography steps, ultrafiltration and diafiltration, micro- and nano- filtration unit operations are highly desired. Demonstrated skills in cross-functional partnerships, supporting cross-functional teams and knowledge of regulatory and cGMP requirements are required. | 6/16/2023 |
| 4571 | Bristol-Myers Squibb Devens, MA Production Engineer/Scientist 1 Bachelor’s degree in Engineering (Chemical, Mechanical, Industrial, Biomedical Engineering) or Life Sciences (Chemistry, Biochemistry, Microbiology) Exp: 0+ years’ |
Reporting to the Shift Manager, Production Engineer/Scientist 1 of the Single Use Facility is responsible for advancing the biologics pipeline according to established work instructions and in accordance with current Good Manufacturing Practices (cGMPs). The role is based in a state of the art facility utilizing single-use technology. The Production Engineer/Scientist 1 is responsible for mastering all routine manufacturing assignments/processes, providing daily technical oversight of execution of manufacturing processes, provide in depth training, maintaining a culture of compliance, and innovation within the downstream team. The Production Engineer/Scientist 1 is required to guide the shift personnel with technical knowledge to lead troubleshooting activities, provide investigation support, analyze process/equipment data, and identify and implement process improvements. | 6/16/2023 |
| 4572 | Bristol-Myers Squibb Warren, NJ Assistant Scientist, Clinical Quality Control- Cell Therapy Bachelor’s degree required, preferably in chemistry, microbiology, or related science. Exp: 0-3 years |
The Assistant Scientist, Clinical QC Sample Management position is responsible for the movement and control of Quality Control (QC) samples and materials in support of the QC laboratories at the CAR T manufacturing facility in Warren, NJ. This primarily includes, but is not limited to, sample collection and distribution, inventory control, chain of custody, sample tracking, documentation, and shipments within the cGMP operation for CTDO Developmental QC for CAR T. | 6/16/2023 |
| 4573 | Covance Greenfield, IN Research Assistant BS/BA degree in science or related field. Exp: 1+ years |
Performs basic laboratory operations independently with detailed review of results by experienced personnel Incumbent has a basic understanding of the technical area of responsibility. | 6/16/2023 |
| 4574 | Covance Herndon, VA Cytotechnologist Bachelors of Science degree in Biology, Chemistry, Medical Technology or Related Life Science. Successful competition of an accredited Cytology progra Exp: New grads welcome! |
$10,000 Sign-On Bonus for External Candidates Only! Are you a certified Cytotechnologist professional, looking for an exciting and challenging change? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a full-time Cytotechnologist in Herndon, VA! This will be a fast paced, customer focused, and challenging environment. LabCorp has a comprehensive benefits package and competitive compensation. LabCorp offers opportunities with advancement potential in an influential and expanding company. Be a part of something where you can make an impact on improving health and improving lives. The work schedule for this position will be: 1st shift, Monday - Friday, 8:00am-4:30pm (ability for flexible start times between 6:00am-9:00am). | 6/16/2023 |
| 4575 | Covance Fort Washington, MD Histotechnician Associate's or Bachelor's Degree in a Life Science and meet local regulatory (CLIA & State) requirements. Histology and/or ASCP certifications are pre Exp: 0+ years |
Process human tissue and body fluid specimens in preparation for microscopic exam Perform technical duties related to the production of histopathological slides of surgical specimens Section the embedded tissue, using a microtome and mount the section properly on a microscope slide Perform various immunohistochemical tests on formalin fixed paraffin embedded tissue sections Process mounted sections through routine and special staining procedures Properly orient and embed surgical tissue specimens Prepare the stains and reagents needed for special procedures Report accurate and timely test results in order to deliver quality patient care | 6/16/2023 |
| 4576 | Covance Baltimore, MD Clinical Laboratory Technologist Associate’s or Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requir Exp: 1+ years |
Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist/Clinical Lab Technician in Baltimore, MD. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. Schedule: 3rd Shift; Mon - Fri (11:30p - 7am); rotating weekends | 6/16/2023 |
| 4577 | Covance Richmond, VA Medical Lab Technologist Exp: |
$2,000 SIGN ON BONUS Are you an experienced Medical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Medical Laboratory Technician OR Technologist in Richmond, VA. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". The schedule for this position is Monday - Friday 7:30a-5:30p, with various start times. This position is a Float opportunity. You will be covering 6 different sites. As a Float Technician, you will be partially reimbursed for your Mileage and receive additional compensation. | 6/16/2023 |
| 4578 | Covance Raritan, NJ Technologist Associate’s or Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requir Exp: 1+ years |
New Grads Welcome – Full Training Provided Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Medical Technologist or Technician in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. The work schedule for this position will be Sun - Thurs - 8:00AM - 4:30PM - With rotating holidays Esoteric/Serology department | 6/16/2023 |
| 4579 | Covance Raritan, NJ Clinical Laboratory Technologist - Immunology Associate’s or Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requir Exp: 1 year |
New Grads Welcome – Full Training Provided Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. The work schedule for this position will be Thursday to Sunday (10.00pm to 8.00am rotating weekend as needed ) | 6/16/2023 |
| 4580 | Exact Sciences San Diego, CA Research Associate II Bachelor’s degree in Life Sciences, Medical Technology, Clinical Laboratory Science, Chemical/Physical/Biological Science, or related field. Exp: 1+ years |
The Research Associate II, with guidance from more experienced scientists, is responsible for the day to day experimentation and is responsible for the execution of bench experiments and analysis of data. Working in a team setting, the Research Associate II will primarily be involved in Research and Development projects assisting in translating research ideas and concepts into the product development pipeline towards development of diagnostic assay products. | 6/16/2023 |
| 4581 | Exact Sciences San Diego, CA Research Associate II Bachelor’s degree in Life Sciences, Medical Technology, Clinical Laboratory Science, Chemical/Physical/Biological Science, or related field. Exp: 1+ years |
The Research Associate II, with guidance from more experienced scientists, is responsible for the day to day experimentation and is responsible for the execution of bench experiments and analysis of data. Working in a team setting, the Research Associate II will primarily be involved in Research and Development projects assisting in translating research ideas and concepts into the product development pipeline towards development of diagnostic assay products. | 6/16/2023 |
| 4582 | Leidos Biomedical Research Groton, CT Chemistry Technician Bachelor's degree in Chemistry or related fields. Exp: 0-2+ years |
Recognized as a Top 10 Health IT provider, the Leidos Health Group draws on decades of success to deliver a range of solutions and services designed to meet the healthcare challenges of today. From the research bench to the patient bedside, we are a company of scientists, engineers, and technologists delivering a broad range of impactful, customizable, and scalable solutions to hospitals and health systems, biomedical organizations, and every U.S. federal agency focused on health. Leidos works with customers across the continuum of care to improve clinical, operational, and financial outcomes with innovative solutions that advance the next generation of care. Our mission is to contribute to creating a healthier world. | 6/16/2023 |
| 4583 | Eli Lilly Cambridge, MA Biologist - Neuroscience Research BSc or MSc in Neuroscience, biological sciences or related fields. Exp: 1+ years |
The Next Generation Therapeutics group is a newly formed team with a focus on using novel therapeutic modalities to deliver medicines for chronic pain and neurodegenerative disorders. The group, based at our Cambridge Innovation Center in Kendall Square, will work with internal and external partners to identify and deliver new novel therapies into patients at speed. The team is seeking experienced and inspiring scientists to join our fast-paced, interdisciplinary team as we leverage innovative RNA/oligonucleotide/gene and genomic based therapeutic modalities to enhance our portfolio. | 6/16/2023 |
| 4584 | Eli Lilly Indianapolis, IN Process Control Engineer Master's degree in Engineering or technology related degree. Exp: 1 year |
The Process Control Engineer provides automation support for manufacturing operations in accordance with appropriate GMP and safety guidelines. This support includes change control implementation, deviation investigation, routine automation computer system support activities, and off hours automation computer system support. The Process Control Engineer also leads non-routine automation computer system support activities, delivers engineering projects to the business, is able to utilize first principles in delivery of these solutions, and can recommend new control strategies for the various chemical processes utilized in manufacturing operations. | 6/16/2023 |
| 4585 | Organogenesis Canton, MA QC Analyst I/II -Microbiology AS or BS degree in a Biology, Chemistry. Exp: 1+ years |
The purpose of this position is the performance and reporting of microbiological testing for product release as well as environmental monitoring of all areas of the manufacturing facility, water sample collection and testing, compilation and entry of environmental monitoring data. The position ensures that the company goals for timely product testing are accomplished by being directly involved in the production of test results for product release and investigations. Other responsibilities or tasks as deemed necessary from time to time by the area’s supervisor. | 6/16/2023 |
| 4586 | Organogenesis Canton, MA Production Associate I - Apligraf Associates or Bachelor’s degree in biology or related science. Exp: 0 - 2 years |
This is an entry level position. The Associate will perform all activities involved in the aseptic processing of a living product (Apligraf), under the direct supervision of the Apligraf Team Leader/Apligraf Supervisor/Manager. The Apligraf Associate I will support the Apligraf Manufacturing department by performing the tasks that will assure the safe and timely processing of Apligraf, working in both a Class 100 and Class 10K cleanroom. | 6/16/2023 |
| 4587 | Meridian Medical Technologies Groton, CT Associate Scientist, Medicinal Chemistry Bachelor’s Degree in chemistry. Exp: 0 to 2 years |
At Pfizer we deliver breakthroughs that change patients’lives. In this job, you'll be joining a team which plays a vital role in this mission through the discovery of Pfizer’s small molecule and syntheticallyderived drugs. In your work, you will be joining a team comprised of experts in the major scientific disciplines involved in the discovery and preclinical development of small molecule drugsincludingmolecular design, synthesis, computational chemistry, pharmacology, chemical biology, structural biology, biophysics, DMPK and analytical chemistry. You will be assisting with the delivery of high-quality drug candidates into the clinic, establishing new drug design approaches and principles, and developing synthetic innovations that drive medicinal chemistry strategies. As an Associate scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. | 6/16/2023 |
| 4588 | Meridian Medical Technologies Pearl River, NY Associate Scientist - Robotics and Automation, Vaccines R&D Bachelor's Degree in?a relevant field of science (biomedical engineering, biology, immunology, microbiology, etc.). Exp: 0-2 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role to participate and operate robotic units in a regulated Good Laboratory Practices (GLP) setting to support Pfizer’s vaccine programs according to Standard Operating Procedures. You will support downstream analyst by doing sample preparation and starting the lifecycle of a sample. You will also spearhead new and innovative projects for process improvement and upkeep of the laboratory. In addition, you will also support throughput activities and provide testing support for clinical and non-clinical research programs. Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. | 6/16/2023 |
| 4589 | Meridian Medical Technologies Pearl River, NY Associate Scientist - Robotics & Automation, Vaccines Bachelor's Degree in a related Science field. Exp: 0-2 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role of executing robotic sample preparation in a regulated Good Laboratory Practices (GLP) setting to support Pfizer’s vaccine programs according to Standard Operating Procedures. In addition, you will also support throughput activities and provide testing support for clinical and non-clinical research programs. Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. | 6/16/2023 |
| 4590 | Meridian Medical Technologies Pearl River, NY Associate Scientist Bachelor's Degree in a related Science field. Exp: 0-2 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role of executing robotic sample preparation in a regulated Good Laboratory Practices (GLP) setting to support Pfizer’s vaccine programs according to Standard Operating Procedures. In addition, you will also support throughput activities and provide testing support for clinical and non-clinical research programs. Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. | 6/16/2023 |
| 4591 | Meridian Medical Technologies McPherson, KS Chemist I (AB2 shift/ 12 hour night shift) Bachelor's Degree in Chemistry or related science field. Exp: 0-1 years |
As part of the Technical Operations team, you are recognized as a subject matter expert with specialized knowledge and skills in procedures, techniques, tools, materials and equipment. You will be entrusted with adapting standard methods and procedures by applying your knowledge, prior work experience and requirements. Your business awareness of cross-organizational impact on project delivery will elevate the quality of project deliverables. You will arrive at decisions on which methods and procedures are the best fit for different work situations. You will train others and reinforce behaviors that will help us achieve our goal of providing the best healthcare to our patients. | 6/16/2023 |
| 4592 | Meridian Medical Technologies McPherson, KS Microbiologist BS/MS in Microbiology or related scientific field. Exp: 0-2 years |
The BQ Lab Analyst I, will perform basic analysis for raw materials, in process and/or finished products in a safe, compliant, and efficient manner. The Job responsibilities include performing microbiological and analytical testing to evaluate the quality of the incoming raw materials and analyze the finished product to demonstrate that the quality of our products meet the high standards of quality. | 6/16/2023 |
| 4593 | Meridian Medical Technologies Rocky Mount, NC Environmental Control Analyst II - Day Shift Bachelor’s Degree in Biology, Microbiology, Chemistry, or similar field. Exp: 0+ years |
You will be a team member who is relied to have a good understanding of procedures, techniques, tools, materials and equipment. Your decision making will help you prioritize workflows based on the available resources. You will follow standard procedures to complete tasks, some of which may vary in scope, sequence, complexity and timing. You will contribute to the team’s success by sharing your previously acquired knowledge. | 6/16/2023 |
| 4594 | Regeneron Tarrytown, NY Assoc. Scientist, Protein Development BS or MS Exp: 0-3+ years |
Regeneron's Protein Development group, a part of our Therapeutic Proteins organization, and located in Tarrytown, NY is seeking an Associate Scientist. In this role, you will drive biochemical characterization of protein reagents and antibodies in support of the company’s VelocImmune fully human antibody pipeline and Immune Oncology programs. | 6/16/2023 |
| 4595 | Regeneron Tarrytown, NY Associate Scientist, Protein Biochemistry BS or MS in Biophysics, Biochemistry, Chemical Engineering, or related field. Exp: 0-2 years |
Regeneron's Protein Biochemistry group, located in Tarrytown is seeking an Associate Scientist who will be responsible for providing in-depth characterization of therapeutic proteins to support research, and late-stage development of various programs. In this exciting role you will be encouraged to participate in method development and technology innovation efforts aimed to improve our understanding and characterization of biotherapeutic proteins. | 6/16/2023 |
| 4596 | Regeneron Tarrytown, NY Associate Scientist, Protein Expression Sciences (PES) M.S. in Molecular Biology, Cellular Biology, Biology or related field. Exp: 0-2 years |
Regeneron is looking for an Associate Scientist to join the Protein Expression Sciences team. | 6/16/2023 |
| 4597 | Regeneron Tarrytown, NY Associate Scientist, Immunology/In Vivo (VI Next) MS in molecular biology, immunology, or related fields. Exp: 0-5 years |
Our group develops and optimizes Regeneron’s mouse platform technologies producing human antibodies and other alternative antibody-based formats. We are seeking and experienced Associate Scientist to join our team to help with cloning projects as well as in vivo mouse immunization and B cell characterization work. | 6/16/2023 |
| 4598 | Regeneron Tarrytown, NY Assoc Scientist, Clinical Bioanalysis BS degree or MS degree in a scientific field. Exp: 0-3+ years |
Regeneron's Clinical Bioanalysis group, located in Tarrytown NY, is seeking an Associate Scientist. | 6/16/2023 |
| 4599 | Aptevo Therapeutics Seattle, WA Assistant Scientist I / II - Immunobiology BS/BA or Master’s degree. AALAS ALAT certification or comparable experience equivalent desired or willing to achieve certification within 6 months of Exp: 1+ years |
The Immunobiology group is seeking an experienced Assistant Scientist to support therapeutic product development by characterizing the biologic activity of bispecific protein therapeutics in pre-clinical research using in vitro and in vivo experimental approaches. She/he will develop and conduct in vitro and ex vivo cellular assays to screen and characterize candidates. Will participate in the planning, execution, analysis, and documentation of experiments. Will work in a collaborative group to provide animal husbandry and maintenance support. Work carefully with in vivo oversight to ensure high quality and compliance. This position will work collaboratively with colleagues across functional groups to provide basic support to pre-clinical research programs. Perform assigned experiments under close or general supervision. Plan and organize details of experiments and keep accurate records. Collaborate with supervisor to develop routine methods. May independently draft basic experimental plans for review with supervisor. Work impacts tasks or initiatives within own group. Provide progress updates to supervisor. | 6/7/2023 |
| 4600 | Arbor Biotechnologies Cambridge, MA Research Associate, Genomic Editing Characterization BS Degree Exp: 0-2 years |
The Arbor Biotechnologies preclinical team is looking to hire a motivated Research Associateto characterize the effectiveness and safety of our novel and proprietary CRISPR-based gene editors.This candidate will help plan, execute, and interpretexperiments that will be used to build Arbor’s portfolio of genetic medicines.He/she/they will have the opportunity to work on multiple lead programs targeting liver and CNS indications. | 6/7/2023 |
| 4601 | Arbor Biosciences Ann Arbor, MI Technical Specialist, Genomics Required: Bachelor’s degree in related field and job experience in life sciences / biotechnology. Preferred: Master’s degree in related field and / or Exp: 1-year |
The Technical Specialist, Genomics is responsible for technical conferrals and support for the Daicel Arbor Biosciences genomics tools and services portfolio, currently including next-generation sequencing kits (myBaits) and laboratory/bioinformatics services (myReads) and cytogenetic probes (myTags). This individual is a core team member supporting Daicel Arbor Biosciences’ essential genomics custom products/services business. This detail-oriented individual should enjoy working with researchers around the world to successfully and efficiently advance their project goals with Daicel Arbor Biosciences products/services. In this role, they serve as a key liaison between clients, account representatives, and internal technical specialty teams. They are knowledgeable about technical applications and scientific usage of Daicel Arbor Biosciences’ NGS and cytogenetics products/services and are able to apply and communicate this knowledge productively to internal and external stakeholders. As needed, they serve as primary technical point of contact for genomics orders that involve technical discussion and/or customization. | 6/7/2023 |
| 4602 | Arrowhead Pharmaceuticals San Diego, CA Research Associate/Associate Scientist, Histology Bachelor in Cell Biology, Molecular Biology, Biochemistry or a related discipline or HT license. Exp: 1-2 years |
The Research Associate/Sr. Research Associate is a member of the Histotechnology team in the Toxicology Department. The Histotechnology team supports the Company’s preclinical drug development efforts by designing studies, collecting, preparing and analyzing samples generated by the Company’s animal studies. The candidate works under the direction of the team lead and employs a wide range routine and non-routine histological methods and analyses. | 6/8/2023 |
| 4603 | Arrowhead Pharmaceuticals Madison, WI Associate Chemist, CMC Process Development BS/BA in Chemistry or related field. Exp: 1 year |
Arrowhead Pharmaceuticals is seeking a highly motivated individual to become a part of its scientific team. We have an immediate opening for an Associate Chemist to work as a Chemist in the Chemistry, Manufacturing, and Controls Group focusing on small molecule process development. This is an ideal position for an individual with an organic chemistry background who has an interest in projects related to novel technology in the synthesis and purification of small molecules and bioconjugates. | 6/8/2023 |
| 4604 | Arrowhead Pharmaceuticals Madison, WI Associate Production Chemist (1st shift) Bachelor’s degree in a scientific field. Exp: Entry level to 5 years |
Arrowhead Pharmaceuticals is seeking a highly motivated individual to become a part of its scientific team. We have an immediate opening for a 1st Shift Associate Production Chemist in the Chemistry, Manufacturing, and Controls Group. | 6/8/2023 |
| 4605 | Arrowhead Pharmaceuticals Madison, WI Associate Production Chemist (2nd shift) Bachelor’s degree in a scientific field. Exp: Entry level to 5 years |
Arrowhead Pharmaceuticals is seeking a highly motivated individual to become a part of its scientific team. We have an immediate opening for a 2nd Shift Associate Production Chemist in the Chemistry, Manufacturing, and Controls Group. 2nd shift work hours are 1 pm – 11:30 pm and include a 12% shift differential. | 6/8/2023 |
| 4606 | Ascent Pharmaceuticals Central Islip, NY Analytical Chemist Bachelor’s degree or foreign equivalent in Pharmacy/Chemistry or related field required. Exp: 1-2 years |
Ascent Pharmaceuticals, Inc. seeks Analytical Chemists for our Central Islip, NY location to develop, validate and conduct inter laboratory transfer of analytical methods for active pharmaceutical ingredients (API) and dosage forms; validate analytical methods and perform quality control activities; research & develop efficient and selective analytical procedures and draft/review laboratory SOPs; design, evaluate and monitor stability programs for drug products; work with advanced analytical equipment; supervise and train chemists and laboratory personnel; test drug substances, intermediates and raw materials while conducting impurity profiles for drug substances and intermediates; prepare ANDAs for FDA submissions etc. | 6/8/2023 |
| 4607 | Ascent Pharmaceuticals Central Islip, NY Manufacturing Chemist Bachelor’s degree or foreign equivalent in Pharmacy/Chemistry or related field required. Exp: 1-2 years |
Ascent Pharmaceuticals, Inc. seeks Manufacturing Chemist for our Central Islip, NY location to plan & coordinate activities related to manufacturing of various dosage forms; develop pharmaceutical dosage forms using advanced scientific techniques; develop new process concepts for product optimization and yield improvement; implement monthly production plans & generate monthly reports; perform IQ, OP & PQ of production equipment; work with product development team to execute bio-batches & validation batches; develop SOPs; draft submissions to regulatory agencies etc. | 6/8/2023 |
| 4608 | Ascent Pharmaceuticals Central Islip, NY Quality Control Chemist Bachelor’s degree or foreign equivalent in Pharmacy/ Chemistry or related field required. Exp: 1-2 years |
Ascent Pharmaceuticals, Inc. seeks Quality Control Chemists in our Central Islip, NY location to perform pharmaceutical laboratory quality control/development activities; develop and validate analytical methods; analyze raw materials and in-process/finished product samples using modern QC techniques; develop/implement & maintain QC systems & activities using advanced analytical lab equipment/ instrumentation; validate & analyze results as per USP, BP, EP, ICH and USFDA guidelines; perform in-process inspections; prepare/implement SOPs; analyze scientific data and prepare detailed QC reports; research, draft and prepare submissions & responses to FDA; update pharma lab equipment/ instrumentation inspection procedures & checklists as necessary etc. | 6/8/2023 |
| 4609 | Ascent Pharmaceuticals Central Islip, NY Quality Assurance Chemist Bachelor’s degree or foreign equivalent in Science/Chemistry or related field required. Exp: 1-2 years |
Ascent Pharmaceuticals, Inc. seeks Quality Control Chemists in our Central Islip, NY location to collaborate with multiple departments including Manufacturing, Facilities, Engineering, Quality Control, Validation, Quality Assurance, and Regulatory to facilitate agreement on equipment, initiation and execution of Product development projects (ANDA Projects), process operational parameters, test requirements and acceptance criteria; Execute Change Controls to allow for the ongoing maintenance and optimization of validated systems and report KPI’s to higher management; Review and approve of a variety of validation lifecycle documents, project plans, user requirement specifications, SOPs, maintenance documentation, investigation reports, deviation resolution, CAPA closeout, etc.; Conduct internal & vendor audits in a group setting & under guidance from senior chemists/scientist for compliance with SOP, CGMP & FDA requirements. Research new regulatory guidance and cGMP and prepare reports for senior scientists and department heads to review and assist in drafting SOP’s; Critically evaluate current processes and continually identify ways to save time and money without sacrificing product quality; Investigate product, and process deviations, identify root cause, and develop corrective and preventative actions; Participate in audits by customers and regulatory agencies and respond to customer complaints in timely manner, review and close out market enquiries & investigations; Assist in APQR, Deviation & Investigation, Risk Assessment, CAPA Management, Change control management, Root Cause Investigation with SPC tools, Market Complaint Handling, Adverse event investigations; Review and Report Process Characterization Protocols, Equipment Qualifications, and review Process Validations of various ANDA drug projects; Conduct internal audits for compliance with SOP, cGMP & FDA requirements. | 6/8/2023 |
| 4610 | Asha Pharma San Diego, CA SR./RESEARCH ASSOCIATE (SAN DIEGO, CA) BS/MS degree in Chemical Engineering, Materials Science, Chemistry, Pharmaceutical Science or related field. Exp: 0-2 years’ |
This position involves working in a laboratory that evaluates novel chemical compounds (typically pharmaceuticals) and discovers novel crystalline structures of the same as part of drug development. The Sr./Research Associate will independently work on projects related to crystallization R&D (e.g. polymorph, salt, cocrystal screening and crystallization process development for pharmaceutical and other molecules) under the guidance of a senior team member. The Sr./Research Associate will also help with Business Development Activities, providing a unique opportunity for well-rounded career development. This position involves working in a laboratory that evaluates novel chemical compounds (typically pharmaceuticals) and discovers novel crystalline structures of the same as part of drug development. | 6/8/2023 |
| 4611 | Astellas South San Francisco, CA Analyst I, QC Microbiology Bachelor’s Degree in chemistry, biology, or microbiology. Exp: 0-3+ years’ |
The primary purpose of the Analyst I position is to Support Quality Control Microbiological testing of drug substances, raw materials, and process intermediates in support of clinical development and commercial programs under cGMP and GLP guidelines. | 6/8/2023 |
| 4612 | Astellas Sanford, NC QC Biochemical Analyst I BS. degree in Biological Sciences. Exp: 0-2+ years |
Analyst I, QC Biochemical, will be responsible for implementing and executing analytical testing in support of clinical and commercial viral vector products in compliance with GMP requirements. Will also support testing for stability studies, methods validation studies and equipment validation. | 6/8/2023 |
| 4613 | Astellas Sanford, NC Analyst I, QC Microbiology BS. degree in Microbiology or other science related degree. Exp: 0-2+ years |
Analyst I QC Microbiology will be responsible for implementing and executing microbiological testing in support of clinical and commercial products in compliance with GMP requirements. This role will also support testing for stability studies, methods validation studies and equipment validation. | 6/8/2023 |
| 4614 | Astellas Seattle, WA Research Associate II, Clinical Gene Editing MS Exp: 0-2 years |
The primary purpose of the Research Associate II for Clinical Gene Editing is to support the generation of clinical-grade, gene-edited Universal Donor Cells in a controlled manufacturing environment. This Research Associate II role will work as part of a team planning and executing all aspects of gene-editing and engineering of pluripotent stem cells. Will assist with complex laboratory operations, keep appropriate documentation including lab notebooks, batch documentation and experimental summaries. Will be able to execute protocols with minimal guidance and will have the ability to summarize results independently. May assist in generating content and preparing controlled documents and data summaries. This position will acquire further versatility in routine procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. | 6/8/2023 |
| 4615 | Astellas Seattle, WA Research Associate II, Clinical Gene Editing MS Exp: 0-2 years |
The primary purpose of the Research Associate II for Clinical Gene Editing is to support the generation of clinical-grade, gene-edited Universal Donor Cells in a controlled manufacturing environment. This Research Associate II role will work as part of a team planning and executing all aspects of gene-editing and engineering of pluripotent stem cells. Will assist with complex laboratory operations, keep appropriate documentation including lab notebooks, batch documentation and experimental summaries. Will be able to execute protocols with minimal guidance and will have the ability to summarize results independently. May assist in generating content and preparing controlled documents and data summaries. This position will acquire further versatility in routine procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. | 6/8/2023 |
| 4616 | Astellas South San Francisco, CA Research Associate II, Discovery Biosciences Master’s Degree in Molecular Biology, Biology, Life Sciences, or a related discipline Exp: 1+ years |
The Research Associate will support the Discovery Bioscience team and assist in developing and executing screening assays for the evaluation of AAV vector products. The Research Associate will be located in our South San Francisco R&D laboratories. | 6/8/2023 |
| 4617 | Astellas South San Francisco, CA Research Associate II, Vector Biosciences Master’s Degree in Molecular Biology, Cell Biology, Life Sciences or a related discipline. Exp: 1+ years |
The Research Associate II will support activities within the Discovery Biology Department. This position involves application of several techniques to produce, purify and characterize AAV viral vectors. The Research Associate will be located in our South San Francisco R&D laboratories. | 6/8/2023 |
| 4618 | Aurora Biolabs San Diego, CA Research Associate I Bachelors or Masters Exp: 0-1 year |
Aurora Biolabs, LLC is seeking a motivated research associate I in cell and molecular biology, biochemistry or related field in San Diego, CA. The individual will be a critical part of our products development team, development a new line of recombinant protein products for drug discovery and commercial use. This position requires extensive hands-on experience with a broad range of techniques including protein expression and purification, molecular cloning, PCR, mammalian cell, insect cells and bacterial culture, ELISA, as well as in vitro cell-based/immuno-based assays. You will work in an atmosphere that is stimulating, innovative, and customer focused. | 6/8/2023 |
| 4619 | Axial Therapeutics Woburn, MA Research Associate/Senior Research Associate - Biosciences Bachelor’s degree in biology, biochemistry, or a related field preferred. Exp: 1-3 years |
In this role the Research Associate will support biology as a member of a highly matrixed drug discovery team and will be responsible for the execution and troubleshooting of various cell-based and biochemical assays and experiments. The Research Associate will contribute to drug screening and mechanism-of-action studies for projects in immuno-oncology and neurological diseases and disorders and have opportunities to contribute to new target discovery and validation. This proactive researcher will collaborate with team members, identify opportunities to improve efficiency, share ideas and expertise and contribute to Axial’s creative, dynamic, and collaborative culture. | 6/8/2023 |
| 4620 | Axis Clinicals USA Dilworth, MN Analytical Chemist I Bachelors degree in Biology, Chemistry, or equivalent. Exp: 1 year |
The Analytical Chemist I, Bioanalytical Operations carries out various Bioanalytical functions of the organization. The Analytical Chemist is responsible for executing Bioanalytical methods within AXIS Clinicals. | 6/8/2023 |
| 4621 | Berkshire Sterile Manufacturing Lee, MA Manufacturing Process Engineer Bachelors’ of Science in Chemical Engineering, Chemistry, Biology or Pharmaceutical Science required or Masters’ in Chemical Engineering, Chemistry, B Exp: Six plus (6+) months |
The Manufacturing Process Engineer will collaborate Process Engineering with tech transfer projects from client or small scale to manufacturing/large scale in a manner that meets safety, quality, and operational performance expectations. The key function of this role is to deliver effective, safe and optimized manufacturing processes for parenteral drug products. | 6/8/2023 |
| 4622 | Berkshire Sterile Manufacturing Lee, MA Process Engineer Process Engineer: Bachelor’s degree in Chemical Engineering, Chemistry, Biology, or Pharmaceutical Science. Exp: One (1) to three (3) years |
The Process Engineer will lead tech transfer projects from client or small scale to manufacturing/large scale in a manner that meets safety, quality, and operational performance expectations. The key function of this role will be to deliver effective, safe and efficient manufacturing processes for parenteral drug products. | 6/8/2023 |
| 4623 | Biocare Medical Pacheco, CA Associate I, Polymer Qualification Bachelor of Science Degree in Biology or a related field. Exp: zero to five (0-5) years’ |
The Associate I, Polymer Qualification functions with minimal supervision and guidance within the research and development (R&D) laboratory. Associate I, Polymer Qualification performs R&D activities on new and existing products involving Immunohistochemistry (IHC) and Protein Chemistry Quality Control (QC) procedures within well-defined guidelines. Associate I, Polymer Qualification keeps abreast of current methodologies and developments within defined areas of research. Antibody Qualification Associate participates in collaborative projects, and at times, assist other laboratory members on research-related activities. | 6/9/2023 |
| 4624 | Biological Dynamics San Diego, CA Research Associate I Bachelor's degree in a scientific discipline. Exp: Entry Level |
The Research Associate is a hands‐on role tasked with experimental work, data acquisition, and basic analysis supporting development of the Company’s proprietary technology programs focused on cancer, neurological, and infectious disease detection. As part of the Research Team, the Research Associate performs studies, supporting the research and development of novel biomarker assays. The Research Associate contributes to the planning, execution, and data analysis of studies under the guidance of senior scientists, supporting growth of IVD products through feasibility to development stages. This hands-on position provides the opportunity to contribute to the development of RUO/LDT products based on an innovative diagnostic platform as part of our growing company. | 6/9/2023 |
| 4625 | Biological Dynamics San Diego, CA Research Associate II Master's degree in Biochemistry, Bioengineering or a related field. Exp: Mid Level |
The Research Associate II is a hands‐on role tasked with experimental work, data acquisition, and basic analysis supporting development of the Company’s proprietary technology programs focused on cancer, neurological, and infectious disease detection. The Research Associate II performs studies supporting the research and development of novel biomarker assays. This position contributes to the planning, execution, and data analysis of studies under the guidance of senior scientists, supporting growth of IVD products through feasibility to development stages. This hands-on position also contributes to the development of RUO/LDT products based on an innovative diagnostic platform as part of our growing company. | 6/9/2023 |
| 4626 | Biomerics Salt Lake City, UT Process Engineer Engineering Degree needed. Exp: 1-3 years |
The Process Engineer will be responsible for supporting and improving the manufacturing of class II medical and surgical devices in a dynamic, customer-focused organization. You will be expected to work with customers to understand product and process specifications, develop manufacturing processes, and build and test devices to those specifications. All activities will be expected to be documented according to design control requirements in a design history file (DHF). The Process Engineer may function as an individual contributor in a small cross-functional team comprised of engineering, operations, and quality members to provide process and manufacturability input to designs throughout the product development process. You will support verification, validation, and regulatory submissions of these devices, then lead the transfer of the products to production and ensure a smooth transition to the production engineering team. | 6/9/2023 |
| 4627 | Novozymes Salem, VA Research Assistant I - Salem, VA Requires a Bachelor's Degree in a scientific discipline. Exp: 1+ years |
Join us as our new Research Assistant Are you ready for a challenging role that lets you use both your scientific grounding and communication skills? Do you have a passion for science and enjoy solving problems that lead to the launch of new products? If so, you could be the Research Assistant we’ve been looking for who can work within the internal process development group, as well as with outside units, to develop advanced and scalable fermentation, recovery, and formulation processes for both existing and novel microbe-based products (i.e., bacteria, fungi, and yeast). This individual will use their in-depth understanding of the scientific principles of microbial fermentation, recovery, formulation, and process development to pioneer research and transform it into value-added products. | 6/9/2023 |
| 4628 | Shape Therapeutics Seattle, WA Research Associate/Sr. Research Associate BS/MS degree in Neuroscience, Molecular/Cellular Biology or related discipline. Exp: 1-3 years |
ShapeTX is looking for a highly motivated and scientifically curious individual to join the Pipeline Research team as a Research Associate / Senior Research Associate. In this role, the successful candidate will primarily conduct in vitro cell-based assays to evaluate novel candidate therapeutics from the ShapeTX RNAfixTM and RNAswapTM technology platform. An ideal candidate will have general cellular and molecular biology experience, a teachable and collaborative spirit, and a desire to work in a fast-paced start-up environment. Neuroscience experience is a plus. This is an excellent opportunity to join the Pipeline Research team and advance the next generation of transformative gene therapies towards the clinic. | 6/9/2023 |
| 4629 | Boston Analytical Salem, NH QC Microbiologist BA or BS degree in Microbiology or related science discipline. Exp: 0-2 years |
The QC Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 6/9/2023 |
| 4630 | Boston Analytical Salem, NH Raw Materials Analytical Chemist I Bachelor’s degree in Chemistry or a related discipline is required. Exp: 0-2 years |
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties include performing analysis of Raw Materials using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development according to USP/EP methods. | 6/9/2023 |
| 4631 | Boston Analytical Salem, NH Microbiologist - Environmental Monitoring BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The EM Microbiologist conducts quantitative and qualitative analysis of pharmaceutical industries Environment according to FDA, ISO, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include Sampling of pharmaceutical industries through ISO standards and client specific test protocols. | 6/9/2023 |
| 4632 | Boston Analytical Salem, NH CHEMIST I Bachelor’s degree in Chemistry or a related science discipline is required. Exp: 0-2 years |
The Analytical Chemist I conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. | 6/9/2023 |
| 4633 | Boston Analytical Framingham, MA Microbiologist EM FTE BA or BS degree in Microbiology or related science discipline. Exp: 0-2 years |
The Environmental Monitoring Microbiologist conducts cleanroom monitoring activities to ensure the air, surfaces, and critical utilities utilized for pharmaceutical product manufacturing meet cGMP requirements. These samples are collected according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. | 6/9/2023 |
| 4634 | Boston Institute of Biotechnology Southborough, MA Research Associate Downstream Process Development BS degrees in biology, biochemistry, biomedical/biochemical engineering, or related fields. Exp: ≤1 year |
A Research Associate I is an entry level position for Bachelor’s degree with no prior experience and reports to a scientist level or above on relevant projects. The individual is responsible for routinely setting up, operating, and maintaining the downstream lab equipment under direct supervision. | 6/9/2023 |
| 4635 | Boston Institute of Biotechnology Southborough, MA Upstream Process Development Research Associate BS degree in Biochemical Engineering or related field of study. Exp: 0-2 years |
Responsibilities 1. Set up, execute, and monitor microbial and mammalian cell culture production in fermenters and bioreactors. 2. Collect, record, and report experimental data. 3. Provide updates to a team lead on a regular basis. 4. Maintain all notebooks and documentation according to department standards. 5. Write SOPs, and batch records. 6. Ability to work well in a team environment and independently as required. 7. Ensure and promote safe environmental and laboratory practices. 8. Order supplies as needed. 9. Prepare solutions and buffers. 10. Maintain lab space and equipment. | 6/9/2023 |
| 4636 | Boston Institute of Biotechnology Southborough, MA Research Associate Analytical Development Bachelor’s or Master’s degree in Biology, Chemistry, Pharmaceutical Sciences, or a related/relevant discipline or demonstrated coursework in such area Exp: Entry Level |
The Research Associate role within Analytical Development is an entry level position for individuals with a Bachelor’s or Master’s degree. Responsibilities include developing analytical methods for biologics characterization, characterizing samples from process development, and supporting subsequent clinical and/or commercial GMP manufacturing. | 6/9/2023 |
| 4637 | BostonGene Waltham, MA Research Associate, Molecular Biology & Next Generation Sequencing Bachelor’s (B.S.) degree in biology, clinical laboratory science, medical technology, or related discipline. Exp: 0-2 years |
ostonGene is seeking a highly motivated Research Associate to join our R&D team in our laboratory located in Waltham, MA. This candidate will support BostonGene’s state-of-the-art primary next-generation sequencing (NGS), adjunct analytical platforms, and automated analysis pipelines. The candidate will be expected to develop proficiencies in NGS support protocols, such as RNA and DNA isolation from tissue, cell-free DNA isolation from plasma, Whole Exome and RNA-Seq library preparation, qPCR, Molecular Biology techniques, and other sample QC techniques. | 6/9/2023 |
| 4638 | BPS Bioscience San Diego, CA Research Scientist I - Cell Biology M.S. Exp: 1+ years |
Perform basic molecular biology, lentivirus production, and stable cell line generation conduct cell-based reporter assays with luciferase and fluorescence as the readout contribute to the development of new lentivirus and cell line products and cell-based assays. | 6/9/2023 |
| 4639 | Alexza Pharmaceuticals Fremont, CA QC Analyst II Master’s degree in science or related field. Exp: 1 year |
Provide timely analyses to support manufacturing and stability. Primary responsibilities include but not limited to physical testing of components and raw materials, in process and release of commercial product or clinical supplies Independently perform assays under GMP, maintaining data integrity and ensuring compliance with company SOPs and specifications Provide accurate, written documentation of all work, including detailed observations and conclusions. Under general guidance, participate in laboratory investigations Independently operate, maintain and troubleshoot laboratory instrumentation and equipment in a safe working environment | 5/31/2023 |
| 4640 | Aptitude Medical Systems Santa Barbara, CA Research Associate Bachelor’s degree or Master’s degree in a relevant discipline. Exp: Entry-Level |
We are seeking to hire multiple capable and driven entry-level Research Associates to join our tight-knit research and development team. In this position, you will be working closely with a cross-functional team of mission-driven scientists and engineers to drive the invention and development of novel diagnostic products. | 5/31/2023 |
| 4641 | Avidity Biosciences San Diego, CA Research Associate, Chemistry BS or MS in chemistry, biochemistry, chemical engineering, or related discipline Exp: 1+ years |
We are seeking a Research Associate to join our team in La Jolla. This is a hands-on position with responsibility for the design, synthesis, and analysis of antibody oligonucleotide conjugates. The ideal candidate will have biotech/pharma experience in aspects of medicinal chemistry, bioconjugation and nucleic acid therapeutics. The candidate is expected to be a strong team player, who enjoys scientific discovery and can communicate and collaborate in an interdisciplinary environment. | 5/31/2023 |
| 4642 | Bio-Concept Laboratories Indianapolis, IN Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 6/1/2023 |
| 4643 | Bio-Concept Laboratories Huntington Beach, CA Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 6/1/2023 |
| 4644 | Bio-Concept Laboratories Redding, CA Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 6/1/2023 |
| 4645 | Bio-Concept Laboratories Woburn, MA Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 6/1/2023 |
| 4646 | Bio-Concept Laboratories Baton Rouge, LA Scientist 1 Associate's degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 6/1/2023 |
| 4647 | Bio-Concept Laboratories Pittsburgh, PA Microbiologist - Scientist Bachelor’s degree in Microbiology, Biology, Chemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the microbiology department of our environmental testing laboratory. | 6/1/2023 |
| 4648 | Bio-Concept Laboratories Springfield, MO Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 6/1/2023 |
| 4649 | BioRestorative Therapies Melville, NY cGMP Bio -Manufacturing Engineer MSc degree in cell biology or similar discipline. Exp: 1 to 6 years |
BioRestorative Therapies, Melville, NY is recruiting for a cGMP bio-manufacturing engineer. This role provides outstanding opportunities for talented self-motivated individuals, ideally with experience in (stem) cell biology, immunology, and/or molecular biology, who can contribute to our ongoing efforts to generate clinical grade cell-based therapeutics. We are most interested in connecting with qualified individuals who aspire to support the development of therapeutics and/or life science products and tools to support research endeavors. | 6/1/2023 |
| 4650 | ChemPacific Baltimore, MD Chemist Master’s degree in Chemistry or Organic Chemistry Exp: one year |
Perform multi-step organic synthesis in solution and/or solid support: Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps such as extraction, recrystallization, silica gel column chromatography and LC/MS purification; perform cGMP synthesis of pharmaceutical ingredients; and perform process development and scale-up for kilogram quantities; and clearly record and communicate results and challenges to coworkers/supervisor. Equipments and tolls used included NMR, UV, MS and IR, Reactor (from 50ml to 221 to 10000l), vacuum pump, water aspirator, condenser, rotavap, voltage transformer, chromatography columns, TLC monitor, lyophilizer, separation funnel and addition funnel. | 6/1/2023 |
| 4651 | CRISPR Therapeutics Boston, MA Research Associate II MS degree in Chemistry, Chemical Engineering, Biochemistry, Bioengineering, Pharmaceutical Sciences or related field. Exp: 0+ years |
We are seeking an experienced Research Associate II to support our analytical biochemistry team. The successful candidate will leverage their technical expertise in analytical chromatography and mass spectrometry to advance our gene editing platform by providing key insights into the synthesis, impurity profile, purification, and structure-activity relationships of oligonucleotides, including gRNA. | 6/1/2023 |
| 4652 | CRISPR Therapeutics Boston, MA Research Associate II, Oligonucleotide Synthesis MS degree in Chemistry, Chemical Engineering, Biochemistry, Bioengineering, Pharmaceutical Sciences or related field. Exp: 0+ years |
CRISPR Therapeutics is seeking a highly motivated Research Associate to join our In Vivo Technical Operations department in Boston, Massachusetts. The incumbent will be responsible for the oligonucleotide synthesis, purification, desalting, and analysis to support the process development of guide RNA production in various scales. This position will also support therapeutic programs in multiple disease areas in R&D department. Prior experience in oligonucleotide synthesis, purification, and characterization is desired. | 6/1/2023 |
| 4653 | CRISPR Therapeutics Framingham, MA Manufacturing Associate Bachelor's degree in biological sciences or related fields. Exp: 1-5 years |
Reporting to the Manufacturing Supervisor, the Manufacturing Associate will perform manufacturing activities associated with immuno-oncology GMP manufacturing within a state-of-the-art manufacturing facility at 33 New York Ave in Framingham, MA. A successful candidate will be responsible for the manufacture of allogenic gene edited cell therapies for clinical studies and as a commercial product. This role requires clear communication across multiple departments for the execution of daily activities. The ideal candidate will have experience successfully performing aseptic cell culture within a GMP environment. | 6/1/2023 |
| 4654 | CRISPR Therapeutics San Francisco, MA Research Associate II, CRISPR-X MS in biology or related disciple. Exp: 0-2 years |
We are seeking a Research Associate II to join the CRISPR X group at CRISPR Therapeutics, the leading gene editing company. The successful candidate will be an integral part of a team whose aim is to advance next generation gene editing. The position requires enthusiasm, passion, attention to detail and a desire to assist in developing the next generation of gene editing. | 6/1/2023 |
| 4655 | Invivotek Hamilton Township, NJ Research Associate (In Vivo/Animal Science) Bachelor of Science degree in Life Science required, Master Degree (Preferred) Exp: 1 to 2 years |
We are seeking a highly motivated and talented individual to join our preclinical in vivo oncology and disease associates’ team. The individual will perform in vivo bioassays on mice and rats in a fast-paced, team-oriented collaborative environment. The candidate should have exceptional skills in basic rodent procedures. Rodent surgery skills are a plus. Experience with biochemical and tissue culture techniques is a plus. Should have a strong foundation in in vivo oncology & disease models. Excellent communication and computer skills. Attention to detail with organizational and record keeping skills. Motivation to learn new assays are essential. Ability to work in a highly interactive and multidisciplinary team environment. Must maintain a professional demeanor and be able to take necessary initiative to meet project timelines and deliverables. | 6/1/2023 |
| 4656 | Invivotek Hamilton Township, NJ Research Associate B.S or M.S. in Molecular Biology, Biochemistry, or a related field. Exp: 1+ years |
Ingenio Diagnostics, a GD3 company, is seeking a motivated Research Associate to support client-driven molecular biology services in Hamilton, NJ. | 6/1/2023 |
| 4657 | Invivotek San Francisco & Sunnyvale, CA Research Associate BS degree in a scientific field. Exp: 1+ years |
Comparative Biosciences, Inc(CBI) a part of Genesis Biotechnology Group is in need of a Research Associate that will assist and execute scientific studies performed at CBI. This will include performing clinical observations of animals and the essential duties and responsibilities required by the facility. | 6/1/2023 |
| 4658 | Invivotek Sunnyvale, CA Research Associate I BS degree in a scientific field. Exp: 1+ years |
Comparative Biosciences, Inc, a member of Genesis Biotechnology Group is looking to grow our team in the Sunnyvale, CA area. We are currently looking for a full time Research Associate I. The ideal candidates for the Research Associate l will assist and execute scientific studies performed at CBI. This will include performing clinical observations of animals and the essential duties and responsibilities required by the facility. | 6/1/2023 |
| 4659 | Invivotek Sunnyvale, CA Research Associate II BS degree in a scientific field. Exp: 1+ years |
Research Associate will assist and execute scientific studies performed at CBI. This will include performing clinical observations of animals and the essential duties and responsibilities required by the facility. | 6/1/2023 |
| 4660 | Invivotek Hamilton , NJ Research Associate I Bachelor of Science degree in Life Sciences. Exp: 1 to 2 years |
We are seeking a motivated and talented Research Associate to develop and perform in vivo and in vitro bioassays on mice and rats. The Research Associate should have excellent skills in basic rodent procedures. Rodent surgery skills are a plus. Experience with biochemical and tissue culture techniques is a plus. Excellent communication and computer skills and motivation to learn new assays are essential. Ability to work in a highly interactive and multidisciplinary team environment. | 6/1/2023 |
| 4661 | Nano Precision Medical Emeryville, CA Analytical Chemist Master’s Degree in chemistry, analytical chemistry, or equivalent discipline. Exp: 1+ years |
This role requires an experienced hands-on analytical chemist who flourishes in a fast-paced start-up environment with shifting priorities and evolving requirements. The AC team provides ongoing analytical services to the R&D and Manufacturing teams, and also develops and transfers new analytical methods and performs one-off special investigations and projects. You’ll be part of a close-knit team of people who are focused, driven, and willing to do whatever it takes to keep the department running. The role requires strong team orientation, flexibility, excellent communication skills, attention to detail, and creative problem solving. | 6/2/2023 |
| 4662 | PL Developments Miami, FL Analytical Scientist I BS or MS in Chemistry Exp: 1-3 years |
Performs testing on raw material, in-process & finished product samples Executes method transfer, verification and validation protocols Documents all data in corresponding laboratory notebook and files documentation according to approved SOP and data integrity guidelines Evaluate and interpret the test results and other related technical documentation Writes methods and reports | 6/2/2023 |
| 4663 | Tanvex BioPharma San Diego, CA Research Associate, Cell Culture Process Development - #1358 BS or advanced degree in chemical/biochemical engineering, cell biology, biochemistry, or related scientific discipline. Exp: 0-3 years |
The Research Associate, Cell Culture Development is responsible for executing individual experiments related to all aspects of cell culture process development of biopharmaceuticals, including media preparation, bioreactor setup, cleaning, sterility and operation, maintaining instruments and equipment, examining data and preparing experiment reports. Applies basic engineering and scientific principles to perform trouble-shooting of processes, instrumentation, and equipment. | 6/2/2023 |
| 4664 | Acceleron Pharma Kenilworth, NJ Scientist, Biologics Analytical Research and Development M.S. in analytical chemistry/biochemistry or related field. Exp: 1+ years |
The Biologics Analytical Research & Development department of our Research & Development Division is seeking applicants for a Scientist position available at its Kenilworth, New Jersey research facility. The Scientist is a laboratory-based scientific role tasked with solving complex analytical problems at the interface of biology, chemistry, and lab informatics disciplines to enable development of Biologics drug substances and drug products. The successful candidate should function well and be able to collaborate in a fast-paced, integrated, multidisciplinary team environment. The qualified candidate will be responsible for development, qualification, implementation, troubleshooting and transfer of analytical methods for monoclonal proteins or other complex therapeutic proteins. Applicants should have effective organizational, multi-tasking, oral/written communications skills, show scientific leadership, and a desire to conduct research and publish. Evidence of strong cross-functional collaboration in an academic or industrial setting is also preferred. | 6/2/2023 |
| 4665 | Acceleron Pharma West Point (PA); Rahway (NJ), PA Scientist - Fermentation, Novel Expression Systems MS with relevant academic or thesis experience in biological engineering, biotechnology, biological science, microbiology, or related field. Exp: 1+ years |
As a member of the Fermentation team in Novel Expression System group, the applicant will serve as an individual scientific contributor as part of a team responsible for bioprocess development and optimization of various expression systems for enzymes, vaccines, and other bioproducts. The candidate is also expected to carry out collaborative research supporting the implementation of these methodologies which involves conceiving, designing, and executing process development experiments. A successful candidate should also have excellent interpersonal, communication and collaboration skills and maintain a focused attention on laboratory safety for everyone on the team. | 6/2/2023 |
| 4666 | Acceleron Pharma West Point , PA SCIENTIST/ENGINEER – UPSTREAM VACCINE PROCESS DEVELOPMENT M.S. in Engineering: Chemical Engineering, Bioengineering, Biomedical Engineering; M.S. in Science and Technology: Cell Biology, Biological Sciences, Exp: one (1) year |
Applications are sought for an opportunity in the Vaccine Process Development (VPD) department, which is part of Our Company's Research Labs division. The individual will support our company's discovery & development efforts for Vaccine programs at West Point, PA. The successful candidate is expected to work with other upstream scientists and engineers, typically focusing on one to two vaccine programs at a time. The candidate will have the ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude. The candidate will have the ability to learn new techniques, to balance multiple projects, to keep accurate records, to follow instructions, and to comply with company policies. The successful candidate will possess proven ability to work in a hands-on laboratory setting and excellent organization, interpersonal, verbal, and written communication skills. | 6/2/2023 |
| 4667 | Acceleron Pharma West Point, PA Associate Specialist, Engineering B.S. or B.A. in Mechanical or Chemical Engineering degree or other science degree Exp: Six plus months |
The Associate Vaccine Manufacturing Technical Support Specialist will provide engineering technical support to the manufacture of liquid vaccines. The role is focused on technical services support with primary focus in the areas of customer complaints, and deviation investigations. The role also encompasses technical services support with primary focus in the areas of deviation management, validation and product franchise support. Specific assignments maybe focused in one area or span across multiple areas of focus. | 6/2/2023 |
| 4668 | Acceleron Pharma Elkhorn, NE Associate Scientist Biology-Discovery Bachelor's degree in biology, microbiology, virology, immunology, or related field. Exp: 1-2 years |
This is primarily a site-based role, under the direction of a supervisor, to conduct laboratory and animal studies for the development of new or improved veterinary or biological products. | 6/2/2023 |
| 4669 | Acceleron Pharma Kenilworth (NJ); Rahway (NJ), NJ Senior Technician Bachelors degree in a related discipline. Exp: 0+ years |
In this role you are expected to work in a team atmosphere in close collaboration with BioProcess development scientists, facility engineering, lab automation and safety groups. We will provide you the necessary on the job training needed to perform laboratory activities. Throughout your career, we will offer you continued development through training classes, workshops, meetings, etc., to improve job skills and product-related procedures. | 6/2/2023 |
| 4670 | Acceleron Pharma Elkton, VA Vaccine Manufacturing Laboratory Technician Bachelor degree. Exp: 1+ years |
The Vaccine Manufacturing Laboratory Technician will work in Technical Operations in support of various Bioprocesses, Fermentation, Biologics Manufacturing, Vaccines Manufacturing, and Wastewater Analysis. | 6/2/2023 |
| 4671 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate, Stem Cell & Gene Therapy Master’s degree in a related field. Exp: up to 2 years |
The Stem Cell and Gene Therapy Advanced Research Associate will be part of a team responsible for the design and development of novel products used in cell and gene therapy workflows, including tools for expansion, identification, and differentiation of immune cells from pluripotent stem cells. Preference will be given to candidates with experience in immunology, particularly lymphocyte cell culture and/or pluripotent stem cell culture. Desirable skills and techniques include 2D and 3D cell culture and bioassays, cell separation, immunostaining, flow cytometry analysis, and molecular biology. | 6/2/2023 |
| 4672 | Advanced Cell Diagnostics Minneapolis, MN Research Associate, Molecular Biology Bachelor’s degree in a science related field. Exp: 0-3 years |
The responsibilities of this position are to assist the Protein Product Development team in the area of recombinant protein expression. This involves the preparation of expression vectors, cell culture, and screening procedures. The position involves various techniques such recombinant DNA cloning, DNA preparation, high-throughput screening, and DNA sequence analysis. It will also include developing new data processing and analysis tools to further enhance our capabilities and platforms. This is an exciting time to join the Protein Development team at Bio-Techne. This position offers a unique opportunity to work hands on in developing cutting-edge technologies and instrumentation. | 6/2/2023 |
| 4673 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate, Molecular Biology Master’s degree in a related field. Exp: up to 2 years |
The responsibilities of this position are to assist the Protein Product Development team in the area of recombinant protein expression. This involves the preparation of expression vectors, cell culture, and screening procedures. The position involves various techniques such recombinant DNA cloning, DNA preparation, high-throughput screening, and DNA sequence analysis. It will also include developing new data processing and analysis tools to further enhance our capabilities and platforms. This is an exciting time to join the Protein Development team at Bio-Techne. This position offers a unique opportunity to work hands on in developing cutting-edge technologies and instrumentation. | 6/2/2023 |
| 4674 | Aerie Pharmaceuticals Fort Worth , TX Associate Scientist Bachelor’s Degree Exp: 1+ years |
We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As an Associate Scientist you will be trusted to assist with key studies supporting Research & Development for Alcon's surgical, vision care, and pharmaceutical divisions. | 6/2/2023 |
| 4675 | Ajinomoto Bio-Pharma Services San Diego, CA QC Chemistry Associate I Bachelor’s degree in a Life Sciences discipline or equivalent preferred. Exp: zero to two years |
We are currently seeking a QC Chemistry Associate I, an entry level position, individual contributor responsible for conducting routine analysis of raw materials, proteins, peptides and small molecules under general supervision for in-process, release and stability testing. May focus in a specialized area and provide routine analysis and testing according to standard operating procedures in any of the following areas: in process and finished formulations. | 6/2/2023 |
| 4676 | Akouos Boston, MA Associate Scientist, Early Preclinical Development BS in life/health sciences required. Exp: 1 to 3 years |
The Early Preclinical Development team is seeking a highly motivated Associate Scientist to assist in and/or conduct in vivo experiments supporting the development of product candidates from early discovery through IND-enabling stages. The successful candidate has in-depth experience in handling mice, including IP administration of medications, and can follow good documentation practices. The successful candidate will be a reliable, flexible team player who enjoys working in a fast-paced environment and is able to multi-task. | 6/2/2023 |
| 4677 | American Regent Columbus, OH QC Chemist I B.S. in Chemistry, Pharmaceutical Science or related field required. Exp: 1+ years |
As part of a team of Analytical Chemists, this position is responsible for performing the analytical activities necessary to support finished product and raw material groups. | 6/2/2023 |
| 4678 | American Regent Columbus, OH QC Chemist I B.S. in Chemistry, Pharmaceutical Science or related field required. Exp: 1+ years |
As part of a team of Analytical Chemists, this position is responsible for performing the analytical activities necessary to support finished product and raw material groups. | 6/2/2023 |
| 4679 | SteriPharma Syracuse, NY Microbiology Analyst (QA/QC), 3rd Shift, Pharma Bachelor’s degree from a regionally accredited institution in science or related field. Exp: 1-3 years’ |
This position performs environmental monitoring and quality control of aseptic process area, to include testing of finished products, raw materials, and components according to established procedures. Position reviews records for accuracy. Position applies standard concepts, practices, and procedures within the laboratory. Position performs a variety of tasks related to both Quality Assurance and Quality Control. | 5/22/2023 |
| 4680 | Strand Therapeutics Boston, MA Associate Scientist, In Vivo Pharmacology - Immuno-Oncology B.S. or M.S. in Biological Sciences, Bioengineering or related discipline. Exp: 1-3 years |
We are looking for an Associate Scientist to join the Translational Biology group to conduct proof-of-concept, validation, and downstream pharmacology studies to support multiple pre-clinical programs. You will be passionate about scientific discovery, undeterred by bold challenges, and enjoy working as a team to develop the next generation of mRNA medicines. You should be highly organized, a critical thinker, adaptable to changing priorities, and possess a strong ability to collaborate effectively with teams of diverse backgrounds. | 5/22/2023 |
| 4681 | Taconic Biosciences Rensselaer, NY Associate Scientist Molecular Analysis Bachelor's degree in the biological field from a four-year college. Exp: 1-year |
The Associate Scientist Molecular Analysis is responsible for providing support of our genotyping operation, preparing next generation sequencing libraries, and developing new techniques. This person will primarily be responsible for genetic characterization of new rodent models. They are responsible for coordinating between departments to ensure project timelines are met and the appropriate tests are conducted. The role also participates in the development of new assays or techniques when additional analysis is needed. Problem solving is a core part of every day, essential for analyzing new results, and to integrate processes within a high throughput testing lab. | 5/23/2023 |
| 4682 | Taconic Biosciences Rensselaer, NY Senior Laboratory Specialist Molecular Analysis - 2nd Shift Bachelor’s Degree from a four-year college or university. Exp: 1-3 years’ |
The Senior Laboratory Specialist performs a variety of molecular assays on animal samples and must be able to generate high-quality results in a timely manner. This individual should be comfortable working in a high-throughput environment and be able to use proper judgement to make technical decisions on assay performance issues. | 5/23/2023 |
| 4683 | Tenaya Therapeutics South San Francisco, CA Research Associate I/II or Senior Research Associate I B.S. or M.S. in pharmacology, biology, physiology, bioengineering or related discipline. Exp: > 1 year |
Tenaya has an immediate need for a Research Associate I to Senior Research Associate I to support the Pharmacology team. The ideal candidate is a self-starter and problem-solver who will work closely with the team to drive the company’s future success. Ideally, you thrive in a fast-paced environment where every day is unique. You are confident, poised and cool-headed, no matter how much is changing around you. You strive for excellence in every facet of your work, and you understand the excitement and commitment of pharmacology roles. Finally, you love being part of a team aligned around a compelling mission. | 5/24/2023 |
| 4684 | Tessera Therapeutics Somerville, MA Research Associate I/II, LNP Formulation (Contractor) BS/MS in Chemistry, Chemical Engineering, Biomedical Engineering, Material Science, or closely related field. Exp: 0-3 years |
This is a contract position with a July target start date, running through the end of the year (with potential to extend or convert). The Research Associate I/II will be responsible for developing LNP formulations and processes to support the company's in vitro and in vivo pre-clinical studies. We are searching for a driven, enthusiastic, and self-motivated individual who is comfortable multitasking and working independently on various aspects of the platform. This individual will join a dynamic, rapidly growing, and highly collaborative team. | 5/26/2023 |
| 4685 | Tessera Therapeutics Somerville, MA Analyst I/II, Quality Control (Contractor) BS/BA degree in biology, chemistry or related field; or MS degree. Exp: BS: 0-2+ years; MS: up to 2 years |
The Quality Control Analyst I/II will be responsible for documentation required for GMP method performance of molecular, plate-based and automated assays. We are searching for a driven, enthusiastic and self-motivated individual who is comfortable multitasking and working independently on various aspects of the platform. This individual will join a dynamic, rapidly growing, and highly collaborative team. The successful candidate will work both independently and as part of a collaborative team to ensure readiness of QC in-process, release and stability test methods used for Tessera drug substances and drug products. This position is a 6-12 month contract role with the possibility of extension/conversion and may leveled up based on years of experience | 5/26/2023 |
| 4686 | Tessera Therapeutics Somerville, MA Research Associate I/II, RNA Production (Contractor) Bachelor's degree or Master's degree in Biochemistry, Molecular Biology, Chemistry, Analytical Chemistry, or related discipline. Understanding of in Exp: BS: 0-4 years ; MS: 0-2 years |
This is a contract position through the end of the year, with a start date of July 11th, 2023 at the earliest. Tessera Therapeutics is seeking a Research Associate I/II for our high-throughput RNA production process. You will support process development for in-vitro transcription, modification, and purification of RNAs to support Tessera's pre-clinical efforts. We seek researchers that are proactive, enthusiastic, and show a passion for process development. The successful candidate should have strong communication and collaboration skills. Strong attention to detail and excellent organizational and documentation skills are highly desirable. | 5/26/2023 |
| 4687 | Tessera Therapeutics Somerville, MA Research Associate/Senior Research Associate, RNA Rewriting Bachelor’s or Master’s degree in biology, cell biology, immunology or a related field. Exp: BS/MS: 0-5 years |
The Research Associate/Senior Research Associate will be responsible for building a next generation screening platform, executing screening workflows, and supporting the team with a focus on molecular and cellular biology in the broader context of applying genome engineering technologies. We are searching for a driven, enthusiastic and self-motivated individual who is comfortable multitasking and working independently on various aspects of the platform. This individual will join a dynamic, rapidly growing, and highly collaborative team. | 5/26/2023 |
| 4688 | TetraGenetics Vancouver, British Columbia, Canada, Ca Research Technician - Sequencing BSc or MSc in Molecular Biology or another relevant field Exp: 1-2 years |
AbCellera is a young, energetic, and rapidly growing tech company with an amazing team that searches, decodes, and analyzes natural immune systems to find antibodies that its partners can develop into drugs to prevent and treat diseases. We are seeking a Research Technician to join our dynamic and multidisciplinary sequencing team. This role is intended for a highly motivated team-player who thrives in a fast-paced work environment with multiple competing priorities, and above all, someone who can learn and grow with us. This is an exciting opportunity to join one of Canada’s most innovative biotech companies and to contribute to our cutting-edge research on antibody engineering, advanced mammalian cell systems, and molecular research supporting the discovery of novel monoclonal antibodies for therapeutic use. | 5/26/2023 |
| 4689 | NeoLight Scottsdale, AZ Biomedical Engineer Bachelor's Degree in Electrical Engineering (Required) from an accredited university or college. Master's degree is preferred. Exp: entry-level |
We seek a full-time entry-level Biomedical Engineer focusing on Electrical Engineering. In this role, you will provide strong, independent technical support to teams that contribute to resolving significant electrical and embedded system issues for the next generation and on-market products. A successful candidate will be a productive individual contributor who works independently with general supervision on larger, moderately complex projects/assignments. In addition, the candidate sets objectives for their job area to meet the objectives of projects and assignments. | 5/26/2023 |
| 4690 | TransMedics Andover, MA Temp-to-Perm Production Test Technician (SECOND SHIFT) BS in Electrical Engineering or equivalent combination of education and experience. Exp: 1+ years |
Responsible for performing testing activities associated with TransMedics’ Organ Care System Hardware and Perfusion Modules. Maintain efforts to ensure all production test related activities are executed in a timely manner to satisfy Company’s Production schedule and quality standards. Assist with maintainance and calibration of equipment used in the testing of electrical components, printed circuit board assemblies and assembled devices per engineering documents and drawings or instructions.Conduct test related activities to support production including but not limited to PCB testing, final system testing, functional testing and burn-in activities. Provide training in testing and inspection methods as required. Maintain individual work area / equipment in a neat orderly manner according to standards including proper disposal of packaging waste, proper storage and use of equipment and parts and management of documentation needed to perform duties. Assist Engineering staff in completion of quality and regulatory activities related to product development, maintenance and/or repair. Assist Test Engineering in the development of new test equipment and protocols. Support Engineering team and Production team efforts to identify opportunities to streamline production through process, test and product design changes. Work with Quality Assurance to maintain an approved internal quality system that meets the requirements of cGMP’s, QSR and ISO requirements. Comply with all work safety rules and regulations. Perform other TransMedics tasks and duties as required. | 5/26/2023 |
| 4691 | Tris Pharma Monmouth Junction, NJ Associate QC Analytical Chemist Bachelors in Chemistry or related scientific field. Exp: 0-3 years |
We have an immediate opening in our Monmouth Junction, NJ QC Lab for an (Associate) QC Analytical Chemist. This is an entry level scientific position and we will train qualified candidates who meet listed requirements. Recent college graduates are welcome to apply. The (Associate) Quality Control (QC) Analytical Chemist performs analytical testing of raw materials, packaging components, in-process (IP), finished product (FP), and/or stability samples (ST). She/he is also responsible for following Analytical Methods, current Good Manufacturing Practices (cGMPs), Protocols, Standard Operating Procedures (SOPs) and company policies. • Carries out responsibilities in accordance with the organization’s policies, SOPs, and state, federal and local laws • Performs testing of raw materials, IP, FP and/or ST samples including dissolution, assay, content/blend uniformity, particle size distribution, and other tests according to the analytical methods, United States Pharmacopeia (USP) procedures in a regulated laboratory environment • Analyzes and interprets test results • Operates general analytical instruments during raw material, IP and FP testing such as High-Pressure Liquid Chromatography (HPLC), Ultra Violet visible spectroscopy (UV/Vis), Automatic Titration, Infra-Red Spectroscopy (IR), Atomic Absorption (AA), Thin Layer Chromatography (TLC) and Dissolution apparatus (distek) • Assists with the identification and troubleshooting of problems with instrumentation and analytical preparations • Meets project deadlines and performance standards as assigned | 5/26/2023 |
| 4692 | TScan Therapeutics Waltham, MA Research Associate/Senior Research Associate, In Vivo Pharmacology (RA07-7 For RA level: BS ; For Sr. RA level: MS Exp: RA: 0-3+ years; Sr. RA level:0-2+ years |
TScan Therapeutics is a startup biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for a motivated researcher to join our In Vivo Pharmacology team as a Research Associate/Senior Research Associate, supporting the preclinical development of our lead therapeutic TCRs. The ideal candidate should have relevant experience in in vivo pharmacology, mechanism of action and anti-tumor efficacy studies, and enjoy fast-paced, collaborative, and vibrant startup culture. A team player with a sense of urgency will thrive in this role. | 5/26/2023 |
| 4693 | Turn Biotechnologies Mountain View, CA Research Associate / Sr. Research Associate - Biology BS/MS in biology, biochemistry, molecular biology, or related discipline. Exp: one year |
Turn Biotechnologies is currently seeking a qualified, highly motivated individual for the position of Sr. Research Associate - Biology. This person will be a highly motivated and responsible individual whose primary purpose is to perform and assist with experiments, analyze data, maintain records, manage projects, maintain lab operations, and other duties as required to meet company goals | 5/26/2023 |
| 4694 | Twist Bioscience Wilsonville, OR Manufacturing Associate Associates or Bachelors degree in Biology, chemistry or related field is desirable. Exp: 1+ years |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations team in Wilsonville, OR. The Manufacturing Associate will produce various DNA and plasmid products, focusing on molecular and cellular biology, as well as running analytic techniques in the high-throughput/highly-automated lab according to established SOPs, along with working with sensitive equipment and following good manufacturing practices. Candidates must also be a team player, neat and highly organized, able to work in a cleanroom environment and foster safe work practices. | 5/26/2023 |
| 4695 | Twist Bioscience Wilsonville, OR Manufacturing Associate - Gene Production Associates or Bachelors degree in Biology, chemistry or related field is desirable. Exp: 1+ years |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations team in Wilsonville, OR. The Manufacturing Associate, Gene Production, will produce various DNA and plasmid products, focusing on molecular and cellular biology, as well as running analytic techniques in the high-throughput/highly-automated lab according to established SOPs, along with working with sensitive equipment and following good manufacturing practices. Candidates must also be a team player, neat and highly organized, able to work in a cleanroom environment and foster safe work practices. | 5/26/2023 |
| 4696 | Twist Bioscience Wilsonville, OR Manufacturing Associate - IgG Production Associates or Bachelors degree in Biology, chemistry or related field is desirable. Exp: 1+ years |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations team in Wilsonville, OR. The Manufacturing Associate, Gene Production, will produce various DNA and plasmid products, focusing on molecular and cellular biology, as well as running analytic techniques in the high-throughput/highly-automated lab according to established SOPs, along with working with sensitive equipment and following good manufacturing practices. Candidates must also be a team player, neat and highly organized, able to work in a cleanroom environment and foster safe work practices. | 5/26/2023 |
| 4697 | Twist Bioscience Wilsonville, OR Manufacturing Associate - Reagents Bachelors/ Associates degree in biology, or relevant field is desirable. Exp: 1+ years |
We are looking for motivated and enthusiastic individuals to join our Twist Bioscience Operations Team in Wilsonville, near Portland, Oregon. The ideal candidate will be driven and will do what it takes to keep synthetic biology manufacturing on track in a fast-paced start-up environment. The Manufacturing Associate for the Reagents group will perform reagent handling, basic chemistry and molecular biology protocols in a high-throughput environment. | 5/26/2023 |
| 4698 | Twist Bioscience South San Francisco, CA Research Associate, Biopharma Libraries Bachelor’s or Master’s degree in Molecular Biology, Biochemistry, Chemistry or closely-related field. Exp: 1-3 years |
We are looking for an outstanding Research Associate (RA) to join our CVL team. The Research Associate will support R&D efforts in developing custom DNA-based applications and assays for combinatorial variant library products. The ideal candidate will be driven and willing to learn new techniques. This position will support projects including high-throughput combinatorial library generation, high-throughput cloning processes, custom molecular biology, NGS-based QC, etc. The ideal candidate will be eager to learn, be very organized, have excellent molecular biology/biochemistry knowledge and skills, and communicate effectively with peers/management. | 5/26/2023 |
| 4699 | Twist Bioscience South San Francisco, CA Research Associate, Process Development B.S. in Molecular Biology, Biochemistry, Bioengineering, or a closely-related field. Exp: 1-2 years |
We are looking for an outstanding Research Associate to join our Process Development Team in South San Francisco. If you thrive in a multidisciplinary team environment where every day is different, excel at executing a variety of processes from the lab bench, and are a creative problem solver with a passion for automation and delivering high quality results, we want you to apply! This position supports development of current and future processes for our synthetic Biology product portfolio which will be transferred to manufacturing teams at Twist. | 5/26/2023 |
| 4700 | United Therapeutics Blacksburg, VA Research Associate I/II - Transplant Research Research Associate I/II - Transplant Research Bachelor’s Degree in Arts/Sciences (BA/BS) in Biology, Cell or Molecular Biology, or Biomedical Sciences Exp: RA I: 1+ years |
The Research Associate I/II will record, collect, and analyze experimental data that is obtained during the testing of various artificial organ constructs. The experiments will include bench-top experiments as well as surgical organ transplantations in large animal models. The Research Associate will interact with several collaboration teams and be trained and educated in how to set up and analyze the required experiments. This position will help to efficiently provide analyses and experimental results that will allow to further improve the function and performance of our artificial organs. | 5/26/2023 |
| 4701 | United Therapeutics RTP, NC Research Associate I/II - Cell Isolation Bachelor’s Degree in Arts/Sciences (BA/BS) in biology, cellular and molecular biology, biomedical sciences, biomedical engineering, or biomanufacturin Exp: RA I: 1+ years |
Conduct and assist in research efforts to develop novel cell and cell-based products for treating pulmonary hypertension and other lung diseases. | 5/26/2023 |
| 4702 | United Therapeutics Manchester, NH Associate Process Engineer/ Process Engineer, Biomaterials Associate Process Engineer: Bachelor’s Degree in Arts/Sciences (BA/BS) in materials science, chemistry, chemical, mechanical or biomedical engineering Exp: APE: 1+ years |
The Associate Process Engineer, Biomaterials (OMG) will be responsible for scaling up and experimenting with large batches of ink to support process and product feasibility goals. This position will also be responsible for periodic quality control (QC) testing. | 5/26/2023 |
| 4703 | Vor Biopharma Cambridge, MA Associate Scientist/Senior Associate Scientist, Discovery & Molecular Engineering Bachelor’s or Master’s degree in molecular biology, biochemistry, genetics, or a related discipline is required. Exp: BS: 0-2+ years’; MS: 1+ years |
Vor Bio is seeking an Associate/Senior Associate Scientist, in the Discovery & Molecular Engineering team. The candidate will contribute towards advancing Vor’s next-generation of genome-engineered hematopoietic stem cells as well as immuno-oncology products using gene editing approaches such as base editing and HDR. The candidate will work in a team environment to execute experimental plans for early discovery research as well as contribute to cell engineering platform development within the Discovery & Molecular Engineering team at Vor. | 5/26/2023 |
| 4704 | Walden Biosciences Cambridge, MA Associate/Research Associate, Cell Systems MS in molecular or cellular biology, or related field. Exp: 0+ years |
As an integral member of our Cell Systems team, the Associate/Research Associate will carry out laboratory research, working collaboratively with the Head of Cell Systems and other members of the Walden Team. This role will contribute to building out the group’s technical capabilities while concurrently undertaking experiments that further our drug discovery programs in vitro and in vivo translational models. | 5/26/2023 |
| 4705 | Zimmer Biomet Warsaw, IN Technician (741378) College/University courses in Microbiology, Biology, Chemistry, Engineering Mechanics, Medical Technology or other related field preferred. Exp: 0 – 3 years |
Responsible for supporting the daily operations of the laboratory at all Zimmer Biomet Warsaw facilities and for operating and maintaining laboratory equipment for the necessary assigned tasks per area work instructions. May also be responsible for ensuring that equipment calibration and maintenance (preventive and/or corrective) is performed. | 5/26/2023 |
| 4706 | Accelerate Diagnostics Tucson, AZ Research Associate, Core Lab Bachelor of Science degree in Microbiology, Molecular Biology, or related life sciences. Exp: 1 year |
The Research Associate is responsible for the routine execution of experiments supporting assay development, technical operations, and core lab. This position can be in different teams including assay development, core lab and technical operations depending upon business needs. | 5/26/2023 |
| 4707 | Accelerate Diagnostics Tucson, AZ Research Associate, Quality Control Bachelor of Science degree in Microbiology, Biochemistry, Molecular Biology, Chemistry, or related life sciences. Exp: 1 year |
The Research Associate for Quality Control is a key member of the Operations Team under the direction of the Team Lead for Consumable Quality Control. This individual will be responsible for testing of incoming product both analytically and biologically in support of manufacturing. This will include, but not limited to, operation of pH/conductivity meter, refractometer and in-house biotechnology systems. This person will be part of a team that executes these tasks on a daily basis. The ideal candidate will be a team player, demonstrate excellent communication skills, be flexible, and excel in a fast-paced environment. | 5/26/2023 |
| 4708 | Ambrix La Jolla, CA Research Associate II, Technology MS degree Exp: 0-4 years |
Ambrx is seeking a highly motivated Research Associate to join the Discovery Group. The primary responsibility is to support multiple oncology and immune-oncology projects from discovery to the preclinical phase. The candidate will work in a multidisciplinary and dynamic team environment to help with discovery and develop precision engineered biological drugs that change patients’ lives. | 5/26/2023 |
| 4709 | Genesis Drug Discovery & Development Hamilton Township, NJ Research Associate (In Vivo/Animal Science) Bachelor of Science degree in Life Science required, Master Degree (Preferred) Exp: 1 to 2 years |
We are seeking a highly motivated and talented individual to join our preclinical in vivo oncology and disease associates’ team. The individual will perform in vivo bioassays on mice and rats in a fast-paced, team-oriented collaborative environment. The candidate should have exceptional skills in basic rodent procedures. Rodent surgery skills are a plus. Experience with biochemical and tissue culture techniques is a plus. Should have a strong foundation in in vivo oncology & disease models. Excellent communication and computer skills. Attention to detail with organizational and record keeping skills. Motivation to learn new assays are essential. Ability to work in a highly interactive and multidisciplinary team environment. Must maintain a professional demeanor and be able to take necessary initiative to meet project timelines and deliverables.We are seeking a highly motivated and talented individual to join our preclinical in vivo oncology and disease associates’ team. The individual will perform in vivo bioassays on mice and rats in a fast-paced, team-oriented collaborative environment. The candidate should have exceptional skills in basic rodent procedures. Rodent surgery skills are a plus. Experience with biochemical and tissue culture techniques is a plus. Should have a strong foundation in in vivo oncology & disease models. Excellent communication and computer skills. Attention to detail with organizational and record keeping skills. Motivation to learn new assays are essential. Ability to work in a highly interactive and multidisciplinary team environment. Must maintain a professional demeanor and be able to take necessary initiative to meet project timelines and deliverables. | 5/26/2023 |
| 4710 | Genesis Drug Discovery & Development Hamilton; Hamilton Township, NJ Research Associate B.S or M.S. in Molecular Biology, Biochemistry, or a related field. Exp: 1+ years |
Genesis Drug Discovery and Development (GD3), an affiliate of the Genesis Biotechnology Group, is a fully integrated contract research organization providing services to support preclinical drug discovery programs from early discovery through preclinical development. Ingenio Diagnostics, a GD3 company, is seeking a motivated Research Associate to support client-driven molecular biology services in Hamilton, NJ | 5/26/2023 |
| 4711 | Genesis Drug Discovery & Development Hamilton, NJ Research Associate M.S. in Organic or Medicinal Chemistry Exp: 1 year |
VENENUM BIODESIGN LLC is member of Genesis Biotechnology Group located in Hamilton, NJ. We are involved in the discovery of novel small molecule therapeutics for a number of diseases. Venenum has openings for Research Associate Chemists to join our Team. As a member of a multi-disciplinary team you will conduct organic syntheses for one or more research projects, focusing on hit to lead and lead optimization. Additionally, you may be involved in library synthesis, or a collaborative project with a partner company. | 5/26/2023 |
| 4712 | Genesis Drug Discovery & Development Hamilton, NJ Research Associate I Bachelor of Science degree in Life Sciences. Exp: 1 to 2 years |
Invivotek LLC, a member of the Genesis Biotechnology Group, is a Contract Research Organization focusing on phenotypic characterization of genetically modified mice and rats and in vivo pharmacology studies, with the emphasis on immunology, oncology, metabolic and neurodegenerative disease. We are seeking a motivated and talented Research Associate to develop and perform in vivo and in vitro bioassays on mice and rats. The Research Associate should have excellent skills in basic rodent procedures. Rodent surgery skills are a plus. Experience with biochemical and tissue culture techniques is a plus. Excellent communication and computer skills and motivation to learn new assays are essential. Ability to work in a highly interactive and multidisciplinary team environment. | 5/26/2023 |
| 4713 | Katalyst Health Cares and Life Sciences South Plainfield, NJ Quality Analyst Master’s degree in pharmacy, biotechnology, chemistry, biochemistry, chemical engineering, mechanical engineering, industrial engineering, biomedical Exp: 6 months |
Responsibilities : Involve in the design, development, implementation, testing, documentation & support of cGxP systems as per 21 CFR Part 11 & US FDA. Responsible for qualification & validation (IQ/OQ/PQ), master plans, protocols, changes requests, gap & root cause analysis, risk management plans, traceability matrix, summary reports for facilities, equipment, systems & processes. Preparation, review, authorize & submission of documentation for quality compliance & regulatory authorities. | 5/26/2023 |
| 4714 | Paraza Pharma Saint - Laurent, QC, Canada, Ca Associate Scientist – Chemical Sciences MSc in Organic, Bioorganic or Medicinal Chemistry Exp: 1+ years |
The Medicinal Chemistry and Chemical Development groups at Paraza are seeking energetic, results-oriented individuals with proven track records of success to join our dynamic teams. The successful candidate is expected to have experience in modern organic synthesis with good laboratory skills and high productivity. The candidate will be expected to work independently within a team structure, design and execute synthetic routes and troubleshoot when needed. | 5/26/2023 |
| 4715 | Sciecure Pharma Monmouth Junction, NJ QC & ARD Chemist Bachelor’s degree from four-year college or university in any of the following disciplines: Chemistry, Biology, Microbiology, or related sciences (as Exp: 1 year |
The Analytical R&D laboratory supports, development and validation of methods analytical test methods, evaluation and testing of raw materials, and testing of non-commercial materials to support product development. All activities are performed in accordance with specifications, standard operating procedures, approved test methods and/or protocols, regulatory requirements. | 5/26/2023 |
| 4716 | Spriaso Salt Lake City, UT Research Chemists Bachelor's degree in chemistry, chemical engineering, biochemistry, or other related degree concentration. Exp: one year |
These positions entails doing product, process, and analytical functions in support of product and technology development under direction of product development and/or analytical leader. The ideal candidate would possess: • Strong computer, scientific, and organizational skills • Excellent communication (oral and written) and attention to detail • Ability to work independently and as part of a team with internal and external clients, self motivation, adaptability, and a positive attitude • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies | 5/26/2023 |
| 4717 | Vaxess Technologies Cambridge, MA Research Associate / Senior Research Associate, Formulation and Analytical Development Master’s degree in one of the Life Sciences, Chemistry, Pharmaceutical Sciences, Chemical Engineering or Biomedical Engineering. Exp: 0-2+ years |
Research & development at Vaxess is cross-disciplinary, integrating biology, chemistry, immunology, materials science, and engineering to address important unmet medical needs in vaccines and therapeutics. We are seeking a talented, collaborative, and highly motivated individual with expertise in formulation and analytical development to join our core team of scientists and engineers. This is a unique opportunity to be part of an emerging early phase clinical company bringing innovative technology to the global market. | 5/26/2023 |
| 4718 | Vaxess Technologies Cambridge, MA Research Associate, Preclinical Studies Master’s degree in one of the Life Sciences. Exp: 0-2+ years |
Research & development at Vaxess is cross-disciplinary, integrating biology, chemistry, immunology, materials science, and engineering to address important unmet medical needs in vaccines and therapeutics. We are seeking a talented, collaborative, and highly motivated individual with expertise in translational animal models and wet lab analytical techniques to join our core team of preclinical scientists and engineers. This is a unique opportunity to be part of an emerging early phase clinical company bringing innovative technology to the global market. | 5/26/2023 |
| 4719 | PsychoGenics Paramus , NJ Research Associate - EEG Bachelors degree in the Biological Sciences or related field. Exp: 1-3 years |
We are looking for a highly motivated Researcher for our EEG group. The successful candidate will work in a team of scientists and researchers supporting preclinical studies using rodent models. The candidate must be capable of working both across teams and independently. | 5/16/2023 |
| 4720 | PsychoGenics Paramus , NJ Research Associate 1 – Surgery/Neuroscience Bachelors degree in life sciences, neuroscience, or psychology. Exp: 1+ years |
We are looking for a highly motivated Research Associate in surgery. The successful candidate will work in a team of scientists and researchers supporting the preclinical studies using rodent models and tests. The primary responsibilities of the candidate will include but are not limited to conducting preclinical research using various surgical procedures primarily in the area of pain, animal disease model, and other drug discovery assays as needed. The candidate will be responsible for surgeries, tissue collection and drug administration, proper execution of experiments, and preliminary data analysis. The candidate must be capable of working across teams and independently. | 5/16/2023 |
| 4721 | PsychoGenics Paramus , NJ Research Associate - Neuropharmacology Bachelors or Masters Degree in the biological sciences, neuroscience, or related field. Exp: 1-3 years |
We are looking for a highly motivated Research Associate in neurodegenerative disorders. The successful candidate will work in a team of scientists and researchers supporting preclinical studies using rodent models. The primary responsibilities of the candidate will include, but are not limited to, dosing animals, conducting behavioral assessments for neurodegenerative disorders, and dissection and tissue collection. The candidate will be responsible for coordinating studies and the proper execution of experiments. The candidate must be capable of working both across teams and independently. | 5/16/2023 |
| 4722 | Proteintech Rosemont, IL Scientist I, Bioconjugation Bachelor’s degree in an appropriate area of specialization (Molecular Biology, Cell Biology, Biochemistry, or related life sciences). Exp: 1+ years |
New grads with lab experience are encouraged to apply. The successful candidate will support the development and optimization of processes in bioconjugation of antibodies for use in various applications like Flow Cytometry and IHC. | 5/16/2023 |
| 4723 | Quansys Biosciences West Logan, UT Formulation Specialist I-II Bachelor’s degree in Biology, Chemistry, Biotechnology, or related field is required. Exp: 1-3 years |
A Formulation Specialist I-II is responsible for meeting production schedules in a fast-paced, high throughput laboratory setting. This is not a production line job. Duties may include the production of immunoassay components, chemical buffers, biological diluents/reagents, coated plates, and/or assembled kits, for customer order fulfillment.They will be responsible, under minimal supervision, to follow established SOPs in order to support the goals of the department. They will be expected to assist in troubleshooting problems and keeping SOPs up to date. Some degree of professional latitude, creativity, and self-management is expected. This position may manage very specific aspects of the manufacturing process within the department. Typically, they will be expected to master at least two aspects of the production process. | 5/17/2023 |
| 4724 | Quansys Biosciences West Logan, UT Quality Control Associate I Bachelor’s degree in Biochemistry, Microbiology, or Chemistry or related field is required. Exp: 0-1 years |
A Quality Control Associate I is responsible for maintaining a high level of quality and customer satisfaction while meeting production schedules in a fast-paced, high throughput industrial setting. Associate will be responsible for the quality control of many product types including chemical buffers, biological diluents/reagents, coated plates, and/or assembled kits, for customer order fulfillment. They will be responsible, under minimal supervision, to follow established SOPs to support the goals of the department. They will be expected to assist in troubleshooting problems and keeping SOPs up to date. Some degree of professional latitude, creativity, and self-management is expected. This position may manage very specific aspects of the QC process within the department. | 5/17/2023 |
| 4725 | Quanterix Billerica, MA Research Associate BS in Chemistry, Biochemistry, Engineering, or Life Science Exp: 0+ years |
We are seeking a well-rounded and highly motivated Research Associate who thrives in a problem-solving oriented position to join our Assay Technical Support team. Key responsibilities will include (1) problem solving escalated issues from manufacturing and quality control, (2) making process improvements identified during investigations, and (3) work as part of the ATS team to drive continuous improvement of the customer experience with Quanterix assays. | 5/17/2023 |
| 4726 | Quanterix Billerica, MA Associate Process Engineer Bachelor’s Degree in Chemistry/Biochemistry/Biology/related field; or Scientific Associate Degree with additional years of relevant experience. Exp: 1+ years |
We are looking for an experienced and motivated Associate Process Engineer in Billerica, MA to join our Pilot Plant team. This position will be responsible for a variety of activities including production of small scale reagents, continuous improvement of existing processes, and establishing manufacturing procedures/work instructions in support of new product in accordance with cGMP. | 5/17/2023 |
| 4727 | Quanterix Billerica, MA Associate Process Engineer Bachelor’s Degree in Chemistry/Biochemistry/Biology/related field; or Scientific Associate Degree with additional years of relevant experience. Exp: 1+ years |
We are looking for an experienced and motivated Associate Process Engineer in Billerica, MA to join our Product Transfer team. This individual will be responsible for a variety of activities including production of small scale reagents, continuous improvement of existing processes, and establishing manufacturing procedures/work instructions in support of new product in accordance with cGMP. | 5/17/2023 |
| 4728 | Quanterix Billerica, MA Research Associate, Product Validation B.S. degree in biological or physical sciences required Exp: 1-3 years |
We are looking for a motivated candidate to join our System Development team. This individual will report to the Associate Director of System Development to provide technical support in Validation testing across Quanterix biomarker systems. This position requires the candidate to collaborate cross-functionally to understand user requirements and implementation details of system changes to support the execution of immunoassay-based test methods that demonstrate continuity of assay performance on the system. The individual will be responsible for reviewing test plans, executing those plans, and documenting test results. To support this, this role will require the candidate to assist in the detailed analysis of assay and equipment performance for both new systems and upgrades to existing systems, inclusive of both hardware and software changes. | 5/17/2023 |
| 4729 | Quidel Carlsbad, CA Associate Process Group Chemist B.S./B.A. Life/Applied Sciences or equivalent experience. Exp: 6 months |
As we continue to grow as QuidelOrtho, we are seeking an Associate Process Group Chemist, in accordance with forecasted requirements, participates in the manufacture of products within QSR and ISO regulations. This position reviews and reconciles documents and work orders, supports assigned projects with supervision, participates in product transfers, supports departmental troubleshooting and process improvement teams, and displays an improving working knowledge of business processes as they relate to manufacturing. This role is located in Carlsbad, CA onsite. | 5/17/2023 |
| 4730 | Quidel Athens, OH Clinical Repository Associate BA/BS in life sciences, similar field or equivalent. Exp: 1+ years |
As we continue to grow as QuidelOrtho, we are seeking a Clinical Biorepository Associate to oversee a system to maintain and coordinate the inventory and processing of biorepository samples and research materials to support clinical operations and new product development. The Clinical Biorepository Associate will receive samples and maintain physical biospecimen freezer inventories. They will work collaboratively with Clinical Operations management and interface with external biorepositories and 3rd party bio-specimen brokers for specimen procurement, as well as clinical collection sites. This is an onsite position in Athens, OH. | 5/17/2023 |
| 4731 | Quidel San Diego, CA Assay Verification and Validation Technician Bachelor’s degree in Biology, Chemistry, Molecular Biology, Biochemistry, or related discipline. Exp: 1-2 years |
As we continue to grow as QuidelOrtho, we are seeking an Assay Verification and Validation (V&V) Technician to be responsible for verification and validation testing of new products and changes to released products. The Assay V&V Technician contributes to verification and validation activities for multiple systems comprised of assays, reagents, consumables, instruments, and software. The role requires a strong detail-focused skill set to execute tests of products exiting development and to further support and improve products within manufacturing. This is an onsite position in San Diego, CA. | 5/17/2023 |
| 4732 | Quidel San Diego, CA Production Chemist Master’s degree in Chemistry, Biological Sciences, or equivalent. Exp: 0-2 years |
As we continue to grow as QuidelOrtho, we are seeking a Production Chemist. Under minimal ongoing supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP under the direction of senior staff including manufacturing products within QSR and ISO regulations. This position will be located onsite in San Diego, CA | 5/18/2023 |
| 4733 | Quidel San Diego, CA Production Chemist Master’s degree in Chemistry, Biological Sciences, or equivalent. Exp: 0-2 years |
As we continue to grow as QuidelOrtho, we are seeking a Production Chemist. Under minimal ongoing supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP under the direction of senior staff including manufacturing products within QSR and ISO regulations. This position will be located onsite in San Diego, CA | 5/18/2023 |
| 4734 | Quidel San Diego, CA Production Chemist Master’s degree in Chemistry, Biological Sciences, or equivalent. Exp: 0-2 years |
As we continue to grow as QuidelOrtho, we are seeking a Production Chemist. Under minimal ongoing supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP under the direction of senior staff including manufacturing products within QSR and ISO regulations. This position will be located onsite in San Diego, CA | 5/18/2023 |
| 4735 | Rani Therapeutics San Jose, CA MECHANICAL ENGINEER Bachelor’s Degree in Mechanical Engineering; or Master’s degree in Mechanical Engineering or equivalent. Exp: BS: 1-3 years |
We are seeking an exceptional Mechanical Engineer to design and develop semi or fully automated equipment that are used for high volume, disposable devices. Your role is to find creative and sound engineering solutions to challenging problems with strong focus on quality, reliability and execution. This is a hands-on position that requires interaction and collaboration with a cross-functional team including Engineering, Manufacturing, Biology, Quality, Facilities and Sustaining. | 5/18/2023 |
| 4736 | Reaction Biology Malvern, PA Research Associate - Biochemical Assays Bachelor’s or master’s degree in biochemistry or related discipline. Exp: 0-2 years |
We are currently seeking a Research Associate for our Malvern, PA facility. We are looking for a reliable and motivated individual with a strong science background to work in our lab. The position is an onsite entry-level bench position with the primary duty of executing a variety of enzymatic assays. | 5/18/2023 |
| 4737 | Recursion Pharmaceuticals Salt Lake City, UT Research Associate, In Vitro (iPSC) Bachelor's or Master's degree in cell biology or related field Exp: 1+ years |
Reporting to our Director, In Vitro, you'll join our newly formed team focused on the utilization of human pluripotent stem cells (hPSCs) to model neurodegenerative diseases. You will be joining a fast-paced team of multi-disciplinary scientists who are focused on bringing new therapeutics to patients at an accelerated pace. This team helps Recursion develop, refine, and characterize state-of-the-art differentiation technology and advanced disease models at a large scale for one of the world’s leading companies in AI-guided drug discovery. This high performing team is bold, creative, and has a team-first mindset alongside a deep passion for exploring the unknowns in neuroscience. | 5/18/2023 |
| 4738 | Minaris Regenerative Medicine Allendale, NJ QA Associate II BS or higher education degree in a scientifically related field. Exp: 1 -3 years |
The Quality Assurance Associate is responsible for performing Quality Assurance activities under direct supervision of daily tasks in support of Quality Systems and/or client procedures including but not limited to document management, review of QC data, material releases and final product releases as well as assisting Quality management with department needs. | 5/19/2023 |
| 4739 | Minaris Regenerative Medicine Allendale, NJ QC Microbiology Analyst I Bachelor's degree in a science or relevant field required. Exp: 0-2 years |
This position will report into the Supervisor of QC Microbiology. The Quality Control Microbiology Analyst I serves as a support role to clinical and/or commercial production. The QC Microbiology Analyst will perform environmental monitoring activities including, but not limited to, non-viable particulate testing, active air viable, passive air viable, surface viable, and personnel monitoring. | 5/19/2023 |
| 4740 | R & D Systems Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
This position is responsible for the developing and or formulation of standards, controls, calibrators, and intermediates in the production and development of Bio-Techne's Luminex, Q-kit, DuoSet, and Simple Plex product lines. Day to day responsibilities involve hands on work in a production laboratory running assays for ELISA and Luminex. You will draft and revise standard operating procedures, manage a production schedule, and analyze assay data to further the ongoing development of new and existing products within Bio-Techne’s evolving portfolio. | 5/19/2023 |
| 4741 | R & D Systems Minneapolis, MN Research Associate, Molecular Biology Bachelor’s degree in a science related field Exp: 0-3 years |
The responsibilities of this position are to assist the Protein Product Development team in the area of recombinant protein expression. This involves the preparation of expression vectors, cell culture, and screening procedures. The position involves various techniques such recombinant DNA cloning, DNA preparation, high-throughput screening, and DNA sequence analysis. It will also include developing new data processing and analysis tools to further enhance our capabilities and platforms. This is an exciting time to join the Protein Development team at Bio-Techne. This position offers a unique opportunity to work hands on in developing cutting-edge technologies and instrumentation. | 5/19/2023 |
| 4742 | R & D Systems Minneapolis, MN Advanced Research Associate, Molecular Biology Master’s degree in a related field Exp: up to 2 years |
The responsibilities of this position are to assist the Protein Product Development team in the area of recombinant protein expression. This involves the preparation of expression vectors, cell culture, and screening procedures. The position involves various techniques such recombinant DNA cloning, DNA preparation, high-throughput screening, and DNA sequence analysis. It will also include developing new data processing and analysis tools to further enhance our capabilities and platforms. This is an exciting time to join the Protein Development team at Bio-Techne. This position offers a unique opportunity to work hands on in developing cutting-edge technologies and instrumentation. | 5/19/2023 |
| 4743 | R & D Systems Minneapolis, MN Advanced Research Associate, Antibody Development Master’s degree in a science related field Exp: 1-2 years |
As an Advanced Research Associate within the Antibody Development Business Unit, you’ll work with and support the mouse hybridoma group at the Minneapolis site which is a critical resource used by various business units - Antibody Development, Protein Development, Immunoassays, QC and Stem cell groups. | 5/19/2023 |
| 4744 | R & D Systems Minneapolis, MN Research Associate, Antibody Development Bachelor’s degree in a scientific discipline or equivalent Exp: 0-2 years |
Key Responsibilities: Mammalian cell culture, including antibody-producing hybridoma cultures. Responsible for rodent immunization and hybridoma fusion Large-scale antibody screening assays. Protein analysis using SDS-PAGE, Western Blot, and ELISA Written and electronic record-keeping of experimentation Follows company policies and practices as outlined in the Handbook and follows guidelines regarding safety as outlined in the AWAIR, Chemical Hygiene and Exposure Control manuals in accordance with the job. Performs additional duties as assigned. | 5/19/2023 |
| 4745 | Roche Carlsbad, CA Research Associate I/II - Assay Development Research Associate I: B.S. in Biochemistry, Molecular Biology, Analytical Chemistry or a related field; Exp: RAI: 0 - 3 years |
Please consider the location of this job will be La Jolla / Torrey Pines. The Research Associate I/II will execute a range of molecular biology and bioanalytical procedures, reagent preparation, and laboratory duties under supervision. You will investigate, adapt or modify experimental methods and technologies for project advancement. This is a unique opportunity to leverage your background and skills in molecular diagnostics to enhance and build your career by working cross-functionally. An exciting career opportunity where your contributions will impact business opportunities through successful completion of projects. | 5/19/2023 |
| 4746 | SAMDI Tech Chicago, IL Research Assistant B.S in biology, biochemistry, chemistry, or related field Exp: 0-3 years |
The Research Assistant will be an active member of our dynamic Research Team. The Research Team leads target/enzyme-based projects for biotech and pharma clients to develop biochemical assays for high-throughput screening and characterization of drug candidates and reaction mechanisms. | 5/19/2023 |
| 4747 | Sarepta Therapeutics Andover, MA Gene Therapy Potency Associate B.S. degree in molecular biology or cell biology Exp: 0 – 2 years |
This individual will support quality control laboratory activities conducted at the Sarepta Andover facility in the field of AAV therapeutic release and stability. The individual will assist in conducting GMP QC release and stability testing using state of art In vitro Potency Assay. The candidate should have hands-on experience in SDS-PAGE, Western blotting, enzyme activity measurements, protein extraction, and quantification methods. The position requires a background in cell culture, tissue lysate sample preparation, protein analysis, and performing assays in a BSL-2 environment. The individual may work under the direction of a subject matter expert conducting experiments and supporting analytical method validation and qualification activities. All aspects of this position involve working in a GMP-compliant manner. This position requires occasional coverage late evening and a few hours on weekends. | 5/19/2023 |
| 4748 | Scanogen Baltimore, MD CHEMICAL AND BIOMOLECULAR ENGINEER Chemical Engineering degree Exp: 1+ years |
Scanogen is looking for a motivated and skilled engineer to join our R&D team. We are a rapidly-growing start-up company developing a nucleic acid detection platform that will change how diseases are diagnosed. We need highly driven and inventive individuals. The main focus is to optimize and automate biomolecule detection assays. | 5/19/2023 |
| 4749 | ScienCell Research Laboratories Carlsbad, CA Associate Molecular Biologist Bachelor’s or Master’s degree in life science. Exp: one-year |
We are searching for an energetic and self-motivated candidate with a positive attitude and strong work ethic to fill our associate molecular biologist position in our R&D department. Responsibilities include, but are not limited to, working on cell-derived DNA, RNA, and proteins purification, gene expression analysis, performing PCR/RT-PCT/qPCR, SDS PAGE and UV spectrum for quantitation. Candidates should be familiar with electrophoresis, spectrophotometer, centrifugation and other basic laboratory techniques. General lab logistical skills such as record keeping, ordering supplies and ensuring general laboratory safety and cleanliness are also required. | 5/19/2023 |
| 4750 | SeaGen Bothell, WA Research Associate B.S. in Chemistry, Biochemistry, or related discipline. Exp: 0-2 years |
Seagen is seeking a Research Associate to participate in the development of drug programs. Responsibilities: Conduct experiments, analyze data and report results to relevant parties to support manufacturing process development. Requirements: BS or MS in chemistry, biochemistry, biological sciences, or a related discipline. Fundamental knowledge of protein chemistry and knowledge related to the detection of protein posttranslational modifications and chemical degradations using bioanalytical techniques. Hands-on analytical experience with liquid chromatography, electrophoretic and other analytical methods (e.g., SEC, RP, CEX, CE-SDS, cIEF). Strong organization and time management skills with attention to detail. Strong desire to achieve team and individual goals in a collaborative team environment. | 5/19/2023 |
| 4751 | SeaGen Bothell, WA Research Associate I Degree in chemistry, biochemistry, chemical engineering or related field, B.S. Exp: 0-2 years' |
The Conjugation Process Development group is seeking a Research Associate I to assist in the development of conjugation processes for antibody-drug conjugates (ADCs). The Research Associate I executes experiments under the direction of others or independently handles those that are routine in nature with minimal variation in design and execution. They compile data in electronic laboratory notebooks and create informative tables and graphs. They occasionally present at group or department meetings. | 5/19/2023 |
| 4752 | SeaGen Bothell, WA Research Associate II M.S. Exp: 0-2 years |
The Research Associate II independently performs standardized experiments with minimal variation in design and execution. They plan and execute more complex experiments under the direction of others. They compile data in electronic laboratory notebooks, create summaries, and analyze data. They occasionally present at group or department meetings. They collaborate cross-functionally and use scientific literature to support experimental work. | 5/19/2023 |
| 4753 | SeaGen Bothell, WA Research Associate II - Pharmacokinetics M.S. Degree in relevant scientific discipline such as: Molecular Biology, Cell Biology, or Biochemistry. Exp: 0-2 years |
The Translational ADME and PKPD (TAPP) group at Seagen is committed to the development of safe and effective therapeutics by characterizing the absorption, distribution, metabolism, elimination and pharmacokinetic-pharmacodynamic relationships of drug candidates in nonclinical species. TAPP collaborates with colleagues across Seagen (early discovery, toxicology, clinical pharmacology, regulatory, etc.) to inform lead selection, conduct nonclinical development studies, and contribute to regulatory filings. The TAPP group is seeking a highly motivated Research Associate to support nonclinical development of large molecule drug candidates. The responsibilities of this role include management of samples, reagents, and mammalian cell cultures as well as execution of cell-based assays. | 5/19/2023 |
| 4754 | SeaGen Bothell, WA Research Associate II, Potency Assays M.S. in Biological Sciences or a related discipline. Exp: 0-2 years |
We are seeking a highly organized and motivated research associate II to join our Potency Assay Development team. The potency team is responsible for the development, qualification, and implementation of cell-based assays, binding assays, and other methods to support lot release and stability testing and the biological characterization of therapeutics in the Seagen pipeline. The ideal candidate for this RAII position should be proficient in cell-based assay development experience, ELISA assay development, cell culture, and cell bank generation. Working experience in potency assays, cytotoxicity assays, live-cell imaging, and flow cytometry is highly desirable. | 5/19/2023 |
| 4755 | SeaGen Bothell, WA Research Associate II, Pharmaceutical Sciences M.S. Degree in Pharmaceutical Sciences, Biochemistry, Biological Sciences, Chemical Engineering, or related discipline. Exp: 0-2 years' |
The Research Associate II independently performs experiments that are routine in nature with minimal variation in design and execution. This role will plan and execute more complex experiments under the direction of others. The Research Associate II compiles data in electronic laboratory notebooks, creates summaries, and analyzes data. This role will occasionally present at group or department meetings. This position collaborates cross functionally and uses scientific literature to support experimental work. | 5/19/2023 |
| 4756 | Seran Bioscience Bend, OR Engineer I Bachelor or Master’s degree in chemical engineering, pharmaceutics, chemistry, bioengineering, mechanical engineering, materials science, physics, or Exp: entry-level |
Serán seeks to hire an entry-level Engineer to contribute in an interdisciplinary team to develop and scale-up pharmaceutical manufacturing processes. The role requires strong hands-on laboratory skills and the ability to apply fundamental scientific principles to solve problems. Strengths in data collection, analysis, proactive communication, and continuous learning by textbooks, journals, and training will enable the successful candidate to thrive. Candidates should possess a bachelor’s or master’s degree in chemistry, chemical engineering, biology, biological engineering, mechanical engineering, materials science and engineering, or physics. Demonstrated research experience is desirable. Candidates with additional relevant experience are also invited to apply. | 5/19/2023 |
| 4757 | Sestina Bio Pleasanton, CA Research Assistant/Research Associate I, Synbio Bachelor’s degree in a scientific discipline or associate degree from a laboratory science or biotechnology program will be considered. Exp: 1+ year |
The Research Assistant/Research Associate I will primarily assist in lab management services such as media preparation, inventory, and shipping & receiving activities. They will report directly to the Laboratory Manager but will have opportunities to cross train and support other groups such as Screening, Analytic Chemistry, and Strain Banking. The successful candidate will be a team player who works within the group to meet department goals, objectives, and tasks to achieve desired results. They can respond to new requests with appropriate urgency and an organized approach and hold themselves accountable to fulfill assigned tasks and achieve results within assigned timelines. | 5/19/2023 |
| 4758 | Smithers Wareham, MA Associate Chemist I - Chemistry - Smithers B.S. degree in chemistry or related field. Exp: 6 months |
Smithers Environmental Risk Sciences division is seeking an Associate Chemist in the Chemistry Department at our Wareham, MA location. Position is expected to perform varied and often complex and difficult procedures somewhat independently. Individual is expected to detect and report problems in standardized procedures due to instrumental, sample, or test system failures. Operates and may maintain, under supervision, test equipment and apparatus of moderate complexity. May provide information for initial data interpretation and test system conformance to expectations. Records, compiles and reduces laboratory data in real time in a complete and thorough manner for individual assignments. May produce reports. | 5/19/2023 |
| 4759 | Pacira Biosciences San Diego, CA QA Associate 1 BS/BA degree in scientific discipline. Exp: 1 year |
This person is to assist and support the organization with GMP compliance, monitoring conformance to established quality assurance processes and GMP standards for manufacturing. | 5/8/2023 |
| 4760 | Pacira Biosciences San Diego, CA QC Analyst 1 BS degree in Chemistry. Exp: 1 year |
The purpose of this position is to carry out assigned laboratory duties which may include sampling, testing, and evaluating analytical data on samples such as raw materials, in-process and final products. | 5/8/2023 |
| 4761 | Pall Danvers, MA Research Associate BSc or BA in a Scientific discipline. Exp: 1 to 4 Years |
Research Associates are responsible for the undertaking of research and development activities to support contracted pharma projects to develop companion diagnostics IVDs. The Research Associate will be responsible for performing required laboratory studies, including making observations, reporting data and providing results to support key decisions within the Pharma Partnerships business unit. A shown ability to communicate (verbal and written) and work with all levels of staff is fundamental to this role. Ensure all work is conducted in accordance with applicable protocols and work instructions and that all work is appropriately documented per procedure. | 5/8/2023 |
| 4762 | Par Pharmaceutical Rochester, MI Quality Associate Specialist, Product Release (Day Shift) BA/BS degree in a related discipline. Exp: 0-1 year |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. All incumbents are responsible for following applicable Division & Company policies and procedures. | 5/8/2023 |
| 4763 | Par Pharmaceutical Rochester, MI Chemist I (Afternoon Shift) Bachelor of Science Degree in chemistry, chemical engineering or related field with analytical chemistry coursework required. Exp: 1+ years |
The Chemist I, under direct supervision, learns and performs QC laboratory chemical analyses of raw materials, in-process materials, stability and finished products, and testing to support process validation. May participate in investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. | 5/8/2023 |
| 4764 | Par Pharmaceutical Rochester, MI Quality Associate Specialist, Product Release - Midnight Shift BA/BS degree in a related discipline. Exp: 0-1 year |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. All incumbents are responsible for following applicable Division & Company policies and procedures. | 5/8/2023 |
| 4765 | Par Pharmaceutical Horsham, PA QC Analyst II – Microbiology M.S. in a Biological Science or related field. Exp: 1-3 years’ |
The QC Analyst II – Microbiology will perform microbiological testing, release of in-process, intermediates and finished products, and testing for validation purposes. This role is responsible for authoring new SOPs and/or revising of existing documentation. Additionally, this role is responsible for writing Deviation Investigations, Laboratory Assessments, and Investigation Reports. | 5/8/2023 |
| 4766 | PreProTech Middleton, WI Associate Scientist Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1+ years |
Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 5/10/2023 |
| 4767 | PreProTech Middleton, WI Associate Scientist Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1+ years |
Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 5/10/2023 |
| 4768 | PreProTech Middleton, WI Associate Scientist Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1+ years |
Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 5/10/2023 |
| 4769 | PreProTech North Chicago, IL Associate Scientist - Sample Management Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1+ years |
Possesses a thorough understanding of sample management processes and works closely with scientists and project managers to ensure samples are received and transferred in accordance with SOPs and study protocols. Develops independence in performing routine work and ability to organize, manage and set priorities for multiple tasks. Demonstrate the ability to document according to ALCOA documentation practices, communicate observations and escalate issues effectively. | 5/10/2023 |
| 4770 | PreProTech Boston, MA Associate Scientist - Analytical Development Bachelor's degree degree in Chemistry, Biochemistry, Chemical Engineering or Pharmaceutical Chemistry. Exp: 0-2 years |
As an Associate Scientist, you will use state-of-the-art technologies to perform traditional and innovative analytical techniques and Quality-by-Design principles to develop and validate the analytical tools used to ensure the safety, efficacy, and quality of the customer pharmaceutical products. As a member of the Analytical Development team, you will provide project support to the drug development programs at the customer site through laboratory techniques commonly used in the analysis of pharmaceuticals such as HPLC,UPLC and Dissolution | 5/10/2023 |
| 4771 | PreProTech Cambridge, MA Associate II, Manufacturing (nights) Bachelor's Degree in STEM or Biotech related Certificate Exp: 1-2 years |
The Formulation Technician II is an associate with a moderate to advanced level of technical expertise and experience. They may independently perform routine operations commensurate with their experience and training. | 5/10/2023 |
| 4772 | Personalis Menlo Park, CA Clinical Lab Associate 1 - Temp (6 months) BA/BS in a biological discipline. Exp: 0-2+ years |
This position is currently in Menlo Park and will be moving to Fremont, You will participate in the daily activities of the laboratory in order to effectively maximize turnaround time, equipment, and material utilization within budgetary constraints while adhering to quality technical standards. | 5/10/2023 |
| 4773 | Personalis Fremont, CA Senior Research Associate, Process Development M.S. Exp: 1-3 years |
The Senior Research Associate within the Process/Product Development group will support the assay development and documentation for new or existing NGS-based products in a regulated environment (FDA-QSR, CLIA, CAP, ISO regulations). This role requires a broad knowledge of molecular biology and assay development techniques. | 5/10/2023 |
| 4774 | Pharmaron Exton, PA Associate Scientist - Permeability Bachelor of Science. Exp: 0-2-year |
Pharmaron (Exton) Lab Services LLC is seeking a candidate to join the Drug Transporter & Cell Manufacturing team to prepare assay solutions, perform cell-based permeability assays, conduct studies, and perform other lab duties. | 5/10/2023 |
| 4775 | Pharmaron Exton, PA Associate Scientist - Permeability Bachelor of Science. Exp: 0-2-year |
Pharmaron Lab Services LLC is seeking a candidate to join the Drug Transporter & Cell Manufacturing team to prepare assay solutions, perform cell-based permeability assays, conduct studies and perform other lab duties. | 5/10/2023 |
| 4776 | Pharmaron Germantown, MD Laboratory Technician Bachelor's degree in related field Exp: 6 months to 1 year |
Come Join Our Growing Team! We are looking for motivated individuals to join our laboratory in Germantown, MD. This is an opportunity for recent graduates to make a real impact in a highly scientific and regulated environment, demonstrate leadership, ambition and the desire to grow with the department. | 5/10/2023 |
| 4777 | Phitonex Middleton, WI Entry Level Scientist Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 5/10/2023 |
| 4778 | Phitonex Richmond, VA Assistant/Associate Scientist Bachelor's degree in Chemistry, Biochemistry, or equivalent and relevant formal academic / vocational qualification. Exp: Assistant Scientist: 0 to 1 year; Associate Scientist: 1+ years. |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 5/10/2023 |
| 4779 | Phitonex Worcester, MA Associate Scientist - Separations and Automation Technologies Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0-2 years |
In this position as an Associate Scientist, you should possess a thorough understanding of laboratory procedures. You will perform a variety of complex sample preparation and analysis procedures to quantitatively measure biopharmaceutical compounds in a variety of biological matrices. Instrumentation is primarily HPLC, CE, and LC/MS. Hamilton Liquid Handlers Protein Maker affinity purification is used as well. Requires following analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against acceptance criteria, methodology, protocol and product specifications. Enters data into databases and reports. | 5/10/2023 |
| 4780 | Phitonex St Louis, MO Cell Culture Technician II (Day Shift) Bachelor’s degree in Biology, Biochemistry or Chemistry seen as a plus. Exp: 1-3 years |
The candidate will be responsible for the performance of operations in support of the manufacture of Commercial and Clinical Biologics. They will be responsible for following Current Good Manufacturing Practices (cGMPs) and carrying out a variety of functions related to Upstream (cell culture) and Downstream (purification) biopharmaceutical manufacturing. These functions may include but are not limited to activities such as propagation of mammalian cell culture, conducting aseptic cell culture operations, execution of large scare production bioreactors (50L - 2000L), conducting large scale chromatography, viral inactivation, viral filtration, ultrafiltration and diafiltration, as well as aseptic filling of bulk drug substance. | 5/10/2023 |
| 4781 | Phitonex Florence, SC Analytical R&D Scientist I Bachelor’s degree in chemistry or related field required. Exp: 1-2 years |
The Scientist I conducts laboratory work as necessary to assure that products are tested per operating procedures. Ensure that work is carried out in an efficient and safe manner. Utilizes judgment in making adaptation and modifications on all assignments. Provides routine analyses in an analytical chemistry laboratory following standard practices. Performs analytical methods as assigned for testing on raw materials, samples, stability, production intermediates, and active pharmaceutical ingredients, including method development and qualification activities. Supports internal development and/or manufacturing operations. Makes detailed observations and reviews, documents, and communicates test results | 5/10/2023 |
| 4782 | Plex Pharma San Diego, CA Research Associate, Biology & Protein Chemistry BS or MS in molecular and biology, protein chemistry or related field. Exp: 1-3 years |
Plex Pharmaceuticals (www.plexpharma.com), a biotechnology company with a focus on developing novel drugs targeting misfolded and aggregated proteins, has an immediate opening for a Research Associate. The successful candidate will contribute to drug discovery efforts by performing cloning, expression and purification of protein drug targets, as well as assisting in assay development and characterization of compounds. | 5/11/2023 |
| 4783 | PPD Cranbury, NJ Scientist I - Protein Production Minimum Bachelor of Science (B.S.) in chemistry or related field Exp: 1+ years |
The Research Scientist I role is responsible for helping to develop recombinant cytokine products for the life-science research market. This role will report to our Director, Lab Operations. Day-shift Opportunity. | 5/11/2023 |
| 4784 | PPD High Point, NC R&D/Manufacturing Scientist II Bachelor’s degree in Pharmaceutical Science, Nanoscience, Chemistry, or related field of study. Exp: 1 year |
Lead technical/scientific project activities applying expertise and experience in the development of appropriate execution strategies and technical solutions to meet client expectations. Lead or participate in technical discussions with client. Engage in the management of clients, processes and equipment design for clinical, scale up and registration batches including tech transfer of projects to and from clients. Lead the design and evaluation of formulations and manufacturing processes and support problem solving as necessary. Manage resources in the function to achieve project and team objectives and coach people in their work group in areas such as the drug development process and DDMT systems. Liaise with Project Management, Facility/Equipment Schedulers, Materials Management, Analytical Development and other functional areas to meet project and team objectives. | 5/11/2023 |
| 4785 | PPD Plainville, MA Scientist I, Upstream Process Development (Viral Vector Services) Bachelor’s Degree in biology, chemistry, biochemistry, (bio)chemical engineering, biomedical engineering, or a related field. Exp: 1+ years’ |
As a member of the Upstream Process Development team, you will have the opportunity to learn to operate cutting-edge instruments and perform activities spanning the full cell line and cell culture production process. This is a hands-on bench scientist position. The ideal candidate shall have excellent lab skills, strong documentation skills, demonstrated ability to analyze and interpret data to draw conclusions and make recommendations, and strong collaboration and teamwork skills. As a member of the Process Development team, you will work with project leads to support the successful execution of experiments and technical transfer activities. This will include supporting the technical transfer process assessments, Pilot Plant activities and transfer into cGMP manufacturing. This will also include late-phase process characterization of viral vector manufacturing processes. | 5/11/2023 |
| 4786 | PPD Lexington, MA Process Engineer I Bachelor’s degree in Mechanical, Chemical, Biochemical/Biomedical, Electrical, or Automation Engineering, or related field of study. Exp: 1 year |
Support the manufacturing operations team to optimize overall equipment efficiency. Support the procurement of new systems, oversee FATs, SATs and Qualification of these new systems, layout configuration for new clients, and PFD development and equipment readiness for tech transfers. Execute process equipment improvement projects stemming from process changes/optimizations, CAPAs, and new capacity demands including compliance item. Drive continuous improvement and operational excellence culture through self-detecting and self-correcting processes and systems and instilling strong ownership and accountability. Ensure high levels of communication with team, support resources, and management regarding issues and resolutions. | 5/12/2023 |
| 4787 | ProteinSimple Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
This position is responsible for the developing and or formulation of standards, controls, calibrators, and intermediates in the production and development of Bio-Techne's Luminex, Q-kit, DuoSet, and Simple Plex product lines. Day to day responsibilities involve hands on work in a production laboratory running assays for ELISA and Luminex. You will draft and revise standard operating procedures, manage a production schedule, and analyze assay data to further the ongoing development of new and existing products within Bio-Techne’s evolving portfolio. | 5/12/2023 |
| 4788 | ProteinSimple San Marcos, CA Chemistry Associate Bachelor’s degree in a related field. Exp: up to 3 years |
This position is responsible for the developing and or formulation of controls, calibrators, working solutions, and intermediates in the production and development of Bio-Techne's various product lines. You will follow standard operating procedures to manufacture these products and will contribute to the ongoing development of new and existing products to help advance Bio-Techne's evolving portfolio. | 5/12/2023 |
| 4789 | ProteinSimple San Marcos, CA Chemistry Associate Bachelor’s degree in a related field. Exp: up to 3 years |
This position is responsible for the developing and or formulation of controls, calibrators, working solutions, and intermediates in the production and development of Bio-Techne's various product lines. You will follow standard operating procedures to manufacture these products and will contribute to the ongoing development of new and existing products to help advance Bio-Techne's evolving portfolio. | 5/12/2023 |
| 4790 | ProteinSimple Minneapolis, MN Quality Technician Position requires an MLT/MLS degree, Bachelor’s degree in Biology, or related field of study. Exp: 0-1 year |
This position will require setup, maintenance, troubleshooting, and operation of QC hematology analyzers. This position will require monitoring instrument performance throughout the QC process and troubleshooting the instrument when necessary. This position will test hematology products for homogeneity during the bottling process by following established methods. The expectation for this position is to setup and QC product on 50% of the laboratory instruments and troubleshoot as necessary. Other tasks include proofing labels and assay sheets. This position will adhere to safety regulations. Perform additional duties as assigned. | 5/12/2023 |
| 4791 | ProteinSimple Minneapolis, MN Advanced Research Associate, Antibody Development Master’s degree in a science related field. Exp: 1-2 years |
As an Advanced Research Associate within the Antibody Development Business Unit, you’ll work with and support the mouse hybridoma group at the Minneapolis site which is a critical resource used by various business units - Antibody Development, Protein Development, Immunoassays, QC and Stem cell groups. | 5/12/2023 |
| 4792 | ProteinSimple Minneapolis, MN Research Associate, Antibody Development Bachelor’s degree in a scientific discipline. Exp: 0-2 years |
Mammalian cell culture, including antibody-producing hybridoma cultures. Responsible for rodent immunization and hybridoma fusion Large-scale antibody screening assays. Protein analysis using SDS-PAGE, Western Blot, and ELISA Written and electronic record-keeping of experimentation Follows company policies and practices as outlined in the Handbook and follows guidelines regarding safety as outlined in the AWAIR, Chemical Hygiene and Exposure Control manuals in accordance with the job. Performs additional duties as assigned. | 5/12/2023 |
| 4793 | Protomer Technologies San Diego, CA Sr. Protein Chemist Master’s Degree in biochemical sciences. Exp: 0-3 years |
We are seeking a highly motivated senior associate scientist with experience in protein purification and characterization to join the Protein Biosciences Group. The successful candidate will have in depth understanding and hands-on experiences in protein purification, and broad knowledge and experience in related fields such as protein expression, analytical and biophysical characterization of proteins. | 5/12/2023 |
| 4794 | Protomer Technologies Pasadena, CA Chemist / Biochemist Undergraduate degree in chemistry, biochemistry, chemical engineering with working knowledge of standard biochemistry or chemistry lab techniques. Exp: 0-3 years |
The ideal candidate will have a bachelor’s or master’s degree in chemistry, chemical engineering, biochemistry, biology, or a related field, as well as in-depth understanding of basic biochemistry and chemistry techniques and experience with development, validation, and implementation of experiments in a biomedical research setting. The applicant must be a fast-learning, task-oriented, and self-motivated person who can perform detailed work with minimal supervision. A requirement of this role is to work well as a team player in a fast-paced research setting. The applicant will be responsible for assisting Protomer’s senior chemists with synthesis, bioconjugation, purification, and characterization of compounds of interest. The successful candidate will actively participate and present in team meetings and is expected to contribute to the team’s progress and success. | 5/12/2023 |
| 4795 | Protomer Technologies San Diego, CA Biologist - In Vitro B.S. in biology, molecular and cellular immunology or a related biological area; Or M.S. in biology, molecular and cellular immunology or a related bi Exp: B.S.: 1-3 years; M.S.: 0-2 years |
The successful biologist will report to a PhD senior scientist in the group located at Lilly in San Diego, CA. You will work in a highly team-oriented and collaborative setting. Working independently to design, develop and validate immunology cell-based functional assays with the goal to deliver preclinical data to support novel therapeutics for future clinical testing will be expected. As a biologist, you will also investigate the mechanism of action of biological and small molecule therapeutics. | 5/12/2023 |
| 4796 | Protomer Technologies San Diego, CA Biologist B.S or M.S in Biological Sciences (Molecular Biology, Protein Biochemistry, Cell Biology) Exp: 0 - 5 Years |
We are looking for a research associate to join our Biotherapeutic Discovery and Research team, with a goal to further our efforts in the discovery and optimization of novel antibodies for therapeutic applications. The successful candidate should possess solid molecular biology, microbiology and laboratory skills and apply theoretical, technical and - if possible - hands-on expertise in protein display/discovery and engineering technologies to help evaluate, optimize and identify lead antibody molecules for clinical development. | 5/12/2023 |
| 4797 | Protomer Technologies San Diego, CA Biologist - Antibody Discovery B.Sc. in Biological Sciences (Biochemistry, Molecular/Cell Biology, Biotechnology or related field) Exp: 1+ years |
We are looking for a highly motivated Biologist with a diversified background in both in vitro biology and biochemical assay development to join our Antibody Discovery group in Biotechnology Discovery Research. The successful candidate will have a strong research background in biochemical and cell-based assays, or other relevant evaluation methods. The successful candidate will join a highly interactive, collaborative, and innovative scientific team to discover and advance large molecule drugs to combat diseases in the diabetes, pain, neurodegenerative and auto-immune areas. The candidate will collaborate with a multidisciplinary team to support the development of therapeutic antibodies and advance technology. | 5/12/2023 |
| 4798 | Protomer Technologies Indianapolis, IN In Vivo Biologist Undergraduate degree in biology/animal science/veterinary technology or a closely related field. Exp: 1-2 years |
The Lilly Diabetes Obesity and Complications Therapeutic Area (DOCTA) is focused on discovery and development of new therapeutics for the treatment of medical complications arising from type 2 diabetes. The cardiorenal team is seeking a highly skilled and motivated biologist to join the discovery research team. This role will craft experiments using animal models of cardiorenal and cardiometabolic diseases. We need a task-oriented and self-motivated biologist who can perform detailed research studies with minimal direction. This will be an opportunity to work cross-functionally within Lilly Research Laboratories and with external collaborators. If you have actively participated in heart failure drug hunting teams and served as a scientific and technical advisor to project teams, we would love for you to apply? Join the Lilly team today! | 5/12/2023 |
| 4799 | Molecular Devices Danvers, MA Research Associate BSc or BA in a Scientific discipline. Exp: 1 to 4 Years |
Research Associates are responsible for the undertaking of research and development activities to support contracted pharma projects to develop companion diagnostics IVDs. The Research Associate will be responsible for performing required laboratory studies, including making observations, reporting data and providing results to support key decisions within the Pharma Partnerships business unit. A shown ability to communicate (verbal and written) and work with all levels of staff is fundamental to this role. Ensure all work is conducted in accordance with applicable protocols and work instructions and that all work is appropriately documented per procedure | 5/3/2023 |
| 4800 | Molecular Devices Coralville, IA Research Scientist II-Enzyme Development Master’s degree (in Biology, Genetics, Chemistry or a related life sciences field). Exp: one or more years |
The Research Scientist II, under minimal direction, conducts bench scientific experimentation that advances the basic science of nucleic acids and nucleic acid biochemistry and assists with the development and characterization of new IDT protein products in the CRISPR, qPCR, and NGS domains. This position is responsible for planning and executing experiments, analyzing data, and reporting/presenting findings as well as supporting IDT customers. A background in bacterial genetics and/or protein engineering is highly preferred. This position is equivalent to a Research Assistant II position at an academic institution. | 5/3/2023 |
| 4801 | Molecular Devices Bellevue, WA Electrical Engineer - Sea-Bird Scientific (Hybrid) Entry-Level: MS Exp: 1 years |
We need an engaged, talented Electrical Engineer to join our Product Development Team! Sea-Bird Scientific develops and manufactures high-accuracy instrumentation for the measurement of ocean parameters. Together we will drive innovation of new products and support the continued evolution of our established instrumentation. The core purpose of this role is to apply your electrical engineering knowledge, with some supervision or guidance, to the design, test, modeling and use of our products, subassemblies, complex systems, and platforms. The successful candidate will report directly to the Electrical Engineering Manager, based at the Bellevue, WA facility. Culture fit, shared values and a belief in our mission are as important to us as your technical ability. Salary will be commensurate with experience, within strictly define ranges.We need an engaged, talented Electrical Engineer to join our Product Development Team! Sea-Bird Scientific develops and manufactures high-accuracy instrumentation for the measurement of ocean parameters. Together we will drive innovation of new products and support the continued evolution of our established instrumentation. The core purpose of this role is to apply your electrical engineering knowledge, with some supervision or guidance, to the design, test, modeling and use of our products, subassemblies, complex systems, and platforms. The successful candidate will report directly to the Electrical Engineering Manager, based at the Bellevue, WA facility. Culture fit, shared values and a belief in our mission are as important to us as your technical ability. Salary will be commensurate with experience, within strictly define ranges. | 5/3/2023 |
| 4802 | Molecular Devices Westborough, MA Scientist I Bachelor’s Degree in biological science, chemical engineering, bioengineering, or relevant field. Master’s Degree preferred. Exp: 1+ years |
Pall has a range of single use bioreactors that is constantly being refined and updated to meet our customer needs. A position has become available for a Scientist I role in Pall’s Biotech R&D Bioprocessing team at the company’s New England Centre of Excellence in Westborough, MA. The team is responsible for process research support for new product developments within Pall. This individual will work closely with Pall colleagues, including R&D, product management, sales, and manufacturing to ensure Pall technologies continue to serve the evolving needs of our customers in the bioprocess industry. | 5/3/2023 |
| 4803 | Molecular Devices Marlborough, Boston, Cambridge, Shr, MA Bioprocess Engineer - Consumables Designer BS in Mechanical / biochemical / chemical engineering or a related engineering/life Science discipline. Exp: 1 year |
** This is a hybrid role with a 1 -4 days in the office a week** We are looking for a Bioprocess Engineer - Consumables Designer to work with our Enterprise Solutions Process and System Design (P&SD) team. Do you have a passion for Consumables Design? Then we would love to hear from you. | 5/3/2023 |
| 4804 | MP Biomedicals Solon, OH Production Chemist Bachelor of Science in Chemistry, Biochemistry, or Biology Exp: 0-3 years |
The production chemist will be trained on two different product lines. This position will rotate training through two manufacturing areas that include Immunology and Molecular Biology Liquids. Learn and be responsible for a wide variety of product formulation tasks. Follow and optimize production processes while following safety protocols. Produce quality research products in a timely fashion to meet customer demand. | 5/5/2023 |
| 4805 | DPT Laboratories Morgantown, WV Chemist I Bachelor's degree (or equivalent). Exp: 0-2 years |
Key responsibilities for this role include: Document laboratory activity in accordance with established procedures; including reagent preparation. Complete training as an Acquisition Controller on LC/MS systems. Demonstrate ability to understand and perform the major types of extraction methodologies employed within the lab Independently perform routine testing proficiently in accordance with all pertinent SOPs and lab practices Process and analyze data according to established procedures. Review data and associated documentation for compliance with Standard Operating Procedures. Operate analytical instrumentation including triple quadrupole HPLC-MS/MS systems and automated liquid handling workstations; including maintenance. | 5/5/2023 |
| 4806 | Nanostring Bothell, WA Manufacturing Research Associate I BS in Molecular Biology, Biochemistry, or related life science. Exp: 0-2 years |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to operate equipment, perform SOPs, navigate Document Control systems, ERP systems, etc. This position is Non-Exempt. | 5/5/2023 |
| 4807 | Nanostring Bothell, WA Manufacturing Research Associate I BS in Molecular Biology, Biochemistry, or related life science. Exp: 0-2 years |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to operate equipment, perform SOPs, navigate Document Control systems, ERP systems, etc. This position is Non-Exempt. | 5/5/2023 |
| 4808 | Nanosyn Santa Clara, CA Associate Research Scientist B.S. in Chemistry, Biochemistry or other relevant discipline. Exp: 0-2 years |
Develop new methods for the synthesis of organic molecules and prepare intermediates for the synthesis of these molecules. Apply modern techniques of organic synthesis including a variety of organic reactions at several scales, inert atmosphere techniques, thin-layer chromatography, NMR, LC-MS, HPLC, MS, flash chromatography, recrystallization, distillation, etc. | 5/5/2023 |
| 4809 | Nanosyn Santa Clara, CA Research Associate / Screening and Compound Profiling BS in Biology, Biochemistry or other relevant discipline. Exp: 0-2 years |
We are currently seeking a highly motivated screening and compound profiling research associate to join our biology department in Santa Clara, CA. The candidate will play a key role in the organization by being responsible for the planning and timely execution of in vitro biochemical and cell-based assays for Nanosyn’s screening and profiling services. He/She will be responsible for consistently generating high quality data and meeting agreed upon timelines. Applicants must have a strong focus on quality and attention to detail, have the ability to work on multiple projects simultaneously, and be productive both independently and as part of a team. The ideal candidate should have good organizational skills, possess good problem solving, communication and interpersonal skills and to adapt rapidly to new challenges. | 5/5/2023 |
| 4810 | NorthEast BioLab Hamden, CT Associate Scientist, Central Laboratory Services B.S. in Physiological Science, Epidemiology, Microbiology, Immunology, Genetics, Biology, Molecular Biology, Cell Biology, Biotechnology, Biochemistry Exp: 1+ years |
Gain an overall understanding of drug development and maintenance of the full chain of sample custody for regulatory compliance Support implementation of Laboratory Information management System (Watson LIMS) for sample management and storage Sample management and reconciliation, kit preparation and verification, and document preparation related to biological sample collection, storage, and shipment for clinical trials Streamline inventory management, consumable ordering, and other documentation requests for Quality Assurance Unit Help maintain ultra-low temperature (ULT) freezers and refrigerators and associated electronic logs and records Learn bioanalytical techniques for the analysis of drug and biomarkers in biological matrices Follow appropriate safety and study requirements by reading, understanding, and following Standard Operating Procedures (SOP), Good Laboratory Practices (GLP) requirements, and Sponsor Study protocols Support business development and marketing activities, foster client relationships, and help onboard new sponsors | 5/5/2023 |
| 4811 | Nephron Pharmaceuticals West Columbia, SC FORMULATION TECHNICIAN I Associate or Bachelor’s Degree preferred Exp: 1+ years |
Position Summary: Dispense and formulate raw materials and operate compounding equipment used in the formulation of a final sterile pharmaceutical product Assist with additional work duties or responsibilities as evident or required | 5/5/2023 |
| 4812 | Nephron Pharmaceuticals West Columbia, SC Microbiology Quality Specialist Bachelor’s degree. Exp: 1 year |
Position Summary: Responsible for timely review of laboratory data, Standard Operating Procedures (SOPs), Equipment Validations, studies, and other documents related to the Microbiology department, as needed. Creates and executes project review plans; ensures timely completion of studies or assigned special projects to meet changing needs, requirements, and deadlines of the Microbiology department. Assists with additional work duties or responsibilities as evident or required. | 5/5/2023 |
| 4813 | Nexcelom Bioscience San Diego, CA Research Associate - Exploratory R&D B. S. or M.S. in Biology, Immunology or another related field. Exp: 1 year |
The Research Assistant will be involved in product development and optimization of cell culture process and new product development. In particular, he/she will be involved in determining the feasibility of new products and new cell culture processes for in-house and custom projects. This role will also be involved in troubleshooting issues associated with cell culture. This role requires mammalian cell culture experience. Knowledge of process development for antibody production, particularly hybridoma, on a small and large scale is a plus. He/she must have excellent organizational skills, attention to detail, and accuracy. Be able to maintain good documentation practices and generate reports. Must be proficient in computer software use (Excel, Word, and PowerPoint). Must be self-motivated and able to multi-task. Must be collaborative and have good communication skills. | 5/5/2023 |
| 4814 | Nexcelom Bioscience Pennington Reserve at Upper Provide, PA Research Specialist BS in Biology, Biochemistry or Chemistry. Exp: 1+ years |
We are looking for a highly motivated candidate to provide critical lab research support at a customer site in Upper Providence, PA. The Research Technician provides support to scientists by managing routine in-laboratory tasks according to Scope of Work (SOW) and specifications agreed on between R&D and PerkinElmer. The Research Technician could cover all or some of the following, and work in either GxP or non-GxP laboratory environments. The Research Technicians SOW will depend on demonstrated skills and experience. A successful candidate should have great attention to detail, outstanding organizational skills, and the ability to communicate effectively and be able to work independently. | 5/5/2023 |
| 4815 | Nexcelom Bioscience San Diego, CA Research Associate I - Diagnostics Bachelor’s degree in a Life Sciences-related field Exp: 1 years |
***Research Associate I and Research Associate II candidates will be considered** BioLegend is seeking a highly motivated Product Development Research Associate to join our Diagnostic Product Development Team. This position will actively participate in the development of flow cytometry reagents for diagnostic use. The responsibilities include: perform experiments, analyze and report results, troubleshoot, manage and maintain documentation. After three months in this role, you should be able to work independently to perform flow cytometry experiments, analyze data and document report. | 5/5/2023 |
| 4816 | Nexcelom Bioscience San Diego, CA Research Associate - Antibody Development Bachelor of Science with a discipline in cell biology, immunology, and biochemistry preferred. Exp: 1-2 yrs |
This person would be responsible for developing phosphosite specific monoclonal antibodies in BioLegend derived from immunized animals by performing antigen preparation, host immunization, bleed analysis, and cell lysate preparation. Techniques involved in this job include antigen formulation, animal immunization and tissue harvesting, cell culture and antibody analysis using ELISA and Western blot techniques. | 5/5/2023 |
| 4817 | Nexcelom Bioscience San Diego, CA Research Associate II- Cell Analysis Bachelor’s Degree in life sciences. Exp: 1+ years |
At BioLegend we develop novel, cutting edge products and offer custom services to help with scientific innovation and discovery. We are currently looking for a talented, detail oriented person to join our growing Product Development team. The potential candidate will assist with development of new products for cell analysis such as antibodies, multi-color panels, and reagents for analysis of cell metabolism and cell imaging. The successful candidate must be a self-motivated, team player, able to communicate effectively with a multi-disciplinary team and must possess excellent organization skills. | 5/5/2023 |
| 4818 | Nexcelom Bioscience San Diego, CA Research Associate - Exploratory R&D B. S. or M.S. in Biology, Immunology or another related field. Exp: 1 year |
The Research Assistant will be involved in product development and optimization of cell culture process and new product development. In particular, he/she will be involved in determining the feasibility of new products and new cell culture processes for in-house and custom projects. This role will also be involved in troubleshooting issues associated with cell culture. This role requires mammalian cell culture experience. Knowledge of process development for antibody production, particularly hybridoma, on a small and large scale is a plus. He/she must have excellent organizational skills, attention to detail, and accuracy. Be able to maintain good documentation practices and generate reports. Must be proficient in computer software use (Excel, Word, and PowerPoint). Must be self-motivated and able to multi-task. Must be collaborative and have good communication skills. | 5/5/2023 |
| 4819 | Novartis Cambridge, MA Research Scientist, Cell and Gene Therapy B.S in in Molecular/Cell Biology, Biochemistry or related field. Exp: 1+ years |
We are seeking a highly motivated scientist to join the Biotherapeutic Engineering and Gene Therapy (BEGT) group within NBC in Cambridge, Massachusetts. The BEGT group drives a diverse portfolio of modalities including therapeutic proteins, multi-specific antibodies, CAR-T, RNA therapeutics and AAV. Through innovative and rational protein design as well as cell and viral engineering, the BEGT group works collaboratively within NIBR to broaden the use of biologics into therapeutic applications where conventional antibodies have limitations. | 5/5/2023 |
| 4820 | Novartis San Diego, CA Research Scientist - In Vivo Pharmacology Bachelor's degree in biomedical research, neuroscience, animal behavior or animal sciences. Exp: 1+ years |
The Neuroscience Disease Area at Novartis is looking for a Research Scientist to perform tissue-based analysis in support of discovery and validation of disease relevant targets and pathways at the San Diego campus primarily focusing on gene therapies. | 5/5/2023 |
| 4821 | Novartis Cambridge, MA Research Scientist, Discovery & Translational Pharmacology BS or MS (or equivalent) in Life Sciences Exp: 1-2 years |
Your responsibilities include, but are not limited to: * Perform animal handling, dosing techniques & tissue collection * Implement ex-vivo bio-analysis on generated samples * Work independently to design, execute and analyze in vivo studies in line with project needs and timelines * Support the development of new in vivo models for chronic kidney diseases and systemic fibrosis * Work in a highly team-orientated and matrix environment * Clearly present results and data to teams within Disease Area X and across NIBR * Work in compliance with the Novartis Code of Conduct and in accordance with Novartis guidelines on health and safety and data recording | 5/5/2023 |
| 4822 | Novartis Cambridge, MA Research Scientist, Biochemistry - CVM MS degree in biochemistry, molecular or cell biology, biophysics, biomedical engineering or a related field; BS degree. Exp: MS: 0 years; BS: 1 year |
We are seeking a highly motivated in vitro Research Scientist to join our Biochemistry team. Here you will advance our understanding of disease biology and the discovery of new drugs, by contributing to target validation, assay development and drug screening efforts throughout the disease area and in collaboration with the larger research organization. | 5/5/2023 |
| 4823 | Novartis Emeryville, CA Research Scientist I, NITD Pharmacology Bachelor’s degree (B.A./B.S.) in biomedical or life sciences field preferred. Exp: 0-2 years |
The NITD Pharmacology group provides high quality in vivo research work and support to enable drug discovery research and development. We are looking for a Research Scientist I to coordinate and run in vivo research studies and projects to support the diverse and exciting project portfolio at NITD. The candidate should be action-oriented, skilled in experimental animal work, and possess a strong scientific background in order to plan, design, coordinate and perform in vivo experiments with high technical and ethical standards. The role will require an ability to work independently as well as in close collaboration with other research scientists. | 5/5/2023 |
| 4824 | Novo Nordisk Fremont, CA Engineer - R&D - CELL THERAPY Bachelor preferred. Degree within biomedical engineering, bioengineering, chemical engineering, or life sciences related area preferred. Exp: 0-1+ years’ |
The Cell Therapy R&D Engineer will help develop advanced cell therapeutics by driving product development activities for medical device and biologic/device combination products. The role is responsible for identifying, investigating, and assessing interactions between components of Novo Nordisk’s cellular products including cells, formulations, and medical devices. The Cell Therapy R&D Engineer works closely with product development teams to evaluate device robustness, assists with specifications and product development, and performs testing. This individual will be the subject matter expert for multiple cell and device evaluation equipment systems chosen by Novo Nordisk for product development. | 5/5/2023 |
| 4825 | Novo Nordisk West Lebanon, NH Cell Therapy Associate Master’s in Cell Biology, Molecular Biology or a closely related field. Exp: one (1) year |
This position has the responsibility of working with senior level Scientists and manufacturing associates to execute process development, scale-up, tech transfers, and validation studies in support of manufacturing or analytics. Additionally, the role will necessitate experimental troubleshooting, GMP documentation and laboratory investigations. The position will require understanding the underlying science of the process and manufacturing equipment, or assay methods and instruments. This position is located in West Lebanon, New Hampshire and will require onsite work. It is a full time (40 hours per week) position and the standard schedule is Monday-Friday 8am to 5pm. | 5/5/2023 |
| 4826 | Novo Nordisk West Lebanon, NH Quality Control Microbiologist Bachelors in a scientific discipline. Exp: 1 year |
This position has primary responsibility to support QC operations in the microbiology or analytical area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. This position carries out routine QC testing and may support sampling, investigations, validations, projects and other related support activities for the manufacturing facility and process. This individual works with supervision on routine tasks and detailed instruction on new tasks. This position is located in West Lebanon, New Hampshire and will require onsite work. It is a full time (40 hours per week) position and the standard schedule is Tuesday-Saturday 8am to 5pm. | 5/5/2023 |
| 4827 | Novo Nordisk West Lebanon, NH Manufacturing Science and Analytical Technology Associate I Bachelor’s degree or equivalent in Biochemistry, Chemistry, Engineering or a closely related field. Exp: one year |
This position has the responsibility of working with senior level Scientists to execute laboratory scale process development or validation studies in support of process or assay development, or process troubleshooting or scale-up. The scientific knowledge in this position will range from familiarity with details of manufacturing process, process chemistries, development studies and relevant assay methods and instruments. This position will be one of the interfaces between MSAT and Manufacturing or Quality. | 5/5/2023 |
| 4828 | Novo Nordisk Clayton, NC Manufacturing Engineer BS in Engineering/related field. Exp: 0-2+ years |
Learning the core processes & methods to improve system & equipment reliability to meet all customer, business & regulatory requirements through the following activities: People Focus, Process Focus, Equipment Focus & Standards “Gatekeeper”. | 5/5/2023 |
| 4829 | Noxilizer Hanover, MD Research and Development Laboratory Scientist Bachelor’s degree in Biology, Biotechnology, Biomedical Engineer, Material Science or related field preferred. Exp: 1 year |
The R&D Lab Scientist is responsible for performing, documenting and reporting microbiological sterilization studies for Noxilizer’s customers. Noxilizer’s customers range from Fortune 500 pharmaceutical, biotech and medical device companies to start-ups that are in the US, Europe and Asia. These studies are the first critical step in the customer’s evaluation of nitrogen dioxide sterilization and their product, as well as an important revenue-generating area for the company. The R&D Laboratory Scientist will join a high-performing team of experts to solve sterilization challenges while they grow their skills for future career opportunities. | 5/5/2023 |
| 4830 | Ocean Ridge Biosciences Concord, OH Lab Technician/Associate Scientist - Genetic Toxicology Bachelor’s degree in biology, microbiology, chemistry or other related field. Exp: 1+ years |
This position will provide technical support for performing standard genetic toxicology assays to include, but not limited to cell-based assays, bacterial reverse mutation assay, rodent (rat and mice) bone marrow and blood based micronucleus assay, as well as other in vitro-related activities. | 5/5/2023 |
| 4831 | Ocean Ridge Biosciences Concord, OH General Lab Technician Required qualifications are a B.S. in a chemistry or related field. Exp: 1+ years |
The ideal candidate will perform general lab functions in support of preclinical drug development/ agrochemical studies in a GLP environment. | 5/5/2023 |
| 4832 | Ocean Ridge Biosciences Exton, PA Lab Technician, BGC Bachelor’s degree in molecular biology, Biology, Biochemistry, Chemical Engineering, Mechanical Engineering, or equivalent. Exp: 1-5 years |
We are looking for a qualified Lab Technician to join our team. The role will perform and support laboratory procedures and controls within Biologics, Gene, and Cell Therapy (BGC) Department to maintain efficiency and compliance for the laboratory. The ideal candidate needs to have an entrepreneurial spirit that enables her/him to wear multiple hats as we scale-up the laboratory business. The candidate will have experience in working in a laboratory environment, preferably within biologics/or GCT lab. The candidate will be well-trained to maintain safety conditions in the lab and expected to be passionate in working in a matrix organization environment. The goal is to optimize lab compliance and maintaining the smooth running of the lab. | 5/5/2023 |
| 4833 | Ocean Ridge Biosciences Concord, OH Entry Level Lab Chemist Required qualifications are a B.S. in a chemistry or related field. Exp: 1+ years |
This position is for an entry level lab chemist. The ideal candidate will help support studies of preclinical drug development in a GLP environment. | 5/5/2023 |
| 4834 | Ocean Ridge Biosciences Hayward, CA Research Assistant-ADME BS in biology, biochemistry and other related fields. Exp: 0-3 years |
We are looking for a highly-motivated Research Assistant to develop and conduct biochemical and cellular assays to evaluate potential therapeutics. Experience in cell line development, ELISA, PBMC biomarker, cell culture, cellular assays, gene expression is desirable. Prior experience in ADME assays including metabolite stability, drug transporter, CYP450, PPB and measurements of physicochemical properties is preferred. The candidate needs to be proficient in assay design, trouble-shooting, data analysis and working with 96-w & 384-w plate-based assays. The candidate needs to have a good understanding of drug discovery processes and experience in a discovery project is preferred. This position requires working with an interdisciplinary team of DMPK scientists, analytical chemists and pharmacologists. | 5/5/2023 |
| 4835 | Ocean Ridge Biosciences Hayward, CA Research Associate-Bioanalytical M.S. degree in related scientific discipline or B.S degree. Exp: 0-3 years |
1)Execute established protocols and methods to assay small molecule compounds, their metabolites, and impurities in various chemical and biological samples. 2)Perform data analysis on LC/MS and HPLC instruments, with the ability to identify and troubleshoot inconsistencies as needed. 3) Perform analytical, pharmacokinetic/pharmacodynamic, metabolism data analysis. 4) Conduct basic method development and validation studies. 5) Conduct trouble-shooting and instrument maintenance of LC/MS. 6) Present and discuss data internally and externally. 7) Write reports under supervision. | 5/5/2023 |
| 4836 | Ology Bioservices Alachua, FL Specialist II, Biomanufacturing (Relocation) B.S. (Science or Engineering) Exp: one year |
Responsibilities and Authority: This position will perform production related activities in the cGMP Manufacturing Core according to established procedures at the Manufacturing Facilities in Alachua (Florida). Perform upstream related activities including cell culture at small and large scale, cell transfection, media and buffer preparation, and bioreactor and fermenter-based production. Perform downstream related activities including chromatography purification, centrifugation and ultracentrifugation, ultrafiltration/diafiltration, and viral clearance. Draft Standard Operation Procedures, Change Controls, and Deviations. Properly disinfect and stage materials into production rooms before the production campaigns. Perform with ordering equipment, installation, qualification, and routine maintenance. Draft and review Production batch records and review executed records. | 5/5/2023 |
| 4837 | Pacific Edge Hummelstown, PA Laboratory Technician Bachelor's degree in medical technology, chemical, physical, or biological sciences. Exp: 1 year |
Pacific Edge Diagnostics USA, an innovative cancer detection testing company is a talented Clinical Laboratory Technician to join this rapidly growing company. The Clinical Laboratory Technician's primary responsibility will be to perform molecular clinical testing (from specimen receipt through reporting patient results), as well as general lab maintenance. | 5/5/2023 |
| 4838 | Pacira Biosciences San Diego, CA Microbiologist 1 BS degree in Microbiology or other life science. Exp: 0 years |
The purpose of the position is to provide technical expertise in the area of pharmaceutical microbiology. The position functions in a cooperative effort to provide quality control and assurance to the operational departments involved in the manufacture of pharmaceutical products. | 5/5/2023 |
| 4839 | Key Tech Baltimore, MD Electrical Engineer (Full-Time & Intern Positions) BS or MS Electrical Engineering degree from leading university/college Exp: Up to five years |
We’re actively hiring for full-time engineers as well as spring, summer and fall interns (electrical, computer, and mechanical) with competitive well paid salaries and benefits. Our interns work on real engineering challenges from day one. Everyone who starts at Key Tech jumps right into interesting, creative high tech work. With a blend of challenging work, smart coworkers, and the best company culture, Key Tech is the right company for you. | 4/24/2023 |
| 4840 | Khloris Biosciences Mountain View, CA Cell Therapy Manufacturing Technician B.S. degree in biology, biochemistry, bioengineering, or related technical field, or equivalent industry experience. Exp: 0-5 years |
Khloris Biosciences, Inc. is seeking innovative and highly motivated cell therapy manufacturing technician to join our team. The selected candidate will work closely with lead manufacturing technicians, scientists, participate in project and team meeting, and work in a multidisciplinary environment. The duties of this position will involve supporting a multidisciplinary manufacturing team in developing Khloris cell therapy platforms. The ideal candidate will have hands-on expertise and comprehensive understanding of cell therapy manufacturing processes. | 4/24/2023 |
| 4841 | Lantheus Medical Imaging Billerica, MA Research Scientist I MS in Chemistry, Pharmaceutics, Engineering or equivalent. Exp: 1-2 years |
Radiochemist/Chemist to conduct radiolabeling studies to support R&D portfolio of new and existing products. Requirements include technical expertise in optimization and troubleshooting of synthesis processes, interaction with and transfer of radiolabeling methodology to contract manufacturing sites, and competency in use of HPLC, UV, radio-detection, LCMS and iTLC methodology. Handling of positron and gamma radionuclides for small scale radiolabeling experiments and analytical analysis of both research and commercial products is required. Communication with contract research organizations required for external studies using R&D test compounds. Data interpretation, issue resolution as needed and final report writing is also required. | 4/24/2023 |
| 4842 | Locus Biosciences Research Triangle Park, NC Preclinical Research Technican BS in biology, chemistry, microbiology, microbial genetics, synthetic biology, genetic engineering or similar fields. Exp: 1-5 years |
Locus Biosciences is seeking a highly motivated and entrepreneurial applicant to join our research and development team as a full-time Research Technician within the Preclinical Animal Models team. This position is well-suited for highly motivated technicians that have a desire to push product development forward into critical preclinical in vitro and in vivo testing across a variety of therapeutic indications. This individual will work directly with scientists in the R&D Department to develop and execute in vivo animal models and analyze tissue samples using various molecular and biochemical assays. The ideal candidate will be well organized and have a scientific background as well as experience with microbiology techniques and in running animal models. Candidates must have the ability to manage multiple concurrent projects, but be flexible, adjusting plans as the data dictates. The individual must be able to communicate effectively and be able to work across interdisciplinary teams. | 4/25/2023 |
| 4843 | Lucigen Petaluma, CA Oligonucleotide Production Technician I - Synthesis -Swing Shift (49908) Bachelors Degree or Master's Degree preferred in Life Sciences. Exp: 0-2 years |
An Oligonucleotide Production Technician I – Synthesis will perform tasks associated with the production of modified oligonucleotides in a high throughput, fast paced, and time sensitive manufacturing environment. This position focuses within the Oligonucleotide Synthesis department. Swing Shift T-F 10a.m. 4/10 hour shifts | 4/26/2023 |
| 4844 | Lucigen Petaluma, CA Oligonucleotide Production Technician I - Pilot Synthesis - Day Shift (4... Bachelors Degree or Master's Degree preferred in Life Sciences. Exp: 0-2 years |
An Oligonucleotide Production Technician I – Synthesis will perform tasks associated with the production of modified oligonucleotides in a high throughput, fast paced, and time sensitive manufacturing environment. This position focuses within the Oligonucleotide Synthesis department. Day Shift M-F 7-3:30p.m. 8 hour shifts | 4/26/2023 |
| 4845 | Lucigen Petaluma, CA Oligonucleotide Production Technician I - Purification- Day Shift (49910) Bachelors Degree or Master's Degree preferred in Life Sciences. Exp: 0-2 years |
An Oligonucleotide Production Technician I – Purification will perform tasks associated with the production of modified oligonucleotides in a high throughput, fast paced, and time sensitive manufacturing environment. This position focuses within the Oligonucleotide Purification department. Day Shift - 7a.m. to 5:30p.m. Tuesday through Friday 4/10's | 4/26/2023 |
| 4846 | Lucigen Petaluma, CA Oligonucleotide Production Technician I - Purification- Swing Shift (49911) Bachelors Degree or Master's Degree preferred in Life Sciences. Exp: 0-2 years |
An Oligonucleotide Production Technician I – Purification will perform tasks associated with the production of modified oligonucleotides in a high throughput, fast paced, and time sensitive manufacturing environment. This position focuses within the Oligonucleotide Purification department. Swing Shift Tuesday - Friday 10a.m. to 8:30p.m. 4/10's | 4/26/2023 |
| 4847 | Lucigen Petaluma, CA Oligonucleotide Production Technician I - Liquid Handling- Day Shift (49... Bachelors Degree or Master's Degree preferred in Life Sciences. Exp: 0-2 years |
An Oligonucleotide Production Technician I – Liquid Handling will perform tasks associated with the production of modified oligonucleotides in a high throughput, fast paced, and time sensitive manufacturing environment. This position focuses within the Oligonucleotide Liquid Handling department. Day Shift M-F 8 hour shifts | 4/26/2023 |
| 4848 | Lucigen Petaluma, CA MSAT Chemist (49589) Bachelors in Science required / Masters in Science preferred in Chemistry, Chemical Engineering or related discipline. Exp: 1 year |
We are looking for a highly motivated chemist, biochemist and/or chemical engineer to join in our newly commissioned state-of-art therapeutic oligonucleotide GMP manufacturing facility in Petaluma, CA. This individual will work in a Process Development lab to support therapeutic oligonucleotide manufacturing process development, transfer, and trouble-shooting production issues. | 4/26/2023 |
| 4849 | Lung Biotechnology Silver Spring, MD Associate I, API Production/Synthetic Chemistry Bachelor’s Degree in Arts/Sciences (BA/BS) in physical or biological sciences. Exp: 1+ years |
Responsible for the production of active pharmaceutical ingredients (API) for three of United Therapeutics' commercial drugs, and other drugs that are in the development phase. This role will perform the production in a kilo lab setting using specific procedures and batch records following US and International guidelines for good manufacturing practices (cGMP) to ensure high-quality production. | 4/26/2023 |
| 4850 | Lykan Bioscience Hopkinton, MA QC Analyst, Microbiology Certificate in Biotechnology or Bachelor's degree in scientific discipline preferred. Exp: 0-7+ years' |
The Quality Control Analyst will be responsible for collection of environmental and raw material samples, sample management activities, and testing of cell therapy in-process, release and stability product samples. He/she will be responsible for reporting of data and writing/revising standard operating procedures (SOPs). He/she may support equipment onboarding and qualification as well as test method qualification in compliance with all applicable quality systems and current cGMPs. | 4/27/2023 |
| 4851 | Lykan Bioscience Hopkinton, MA Cell Processing Associate Bachelor's degree in biology or related scientific discipline. Exp: 0-2 years |
Reporting to the Manufacturing Supervisor, this position's core responsibilities are focused on manufacturing processes related to cell therapies. Activities include aseptic sampling of product in a Biosafety Cabinet (BSC) in an ISO V environment, operation of incubators in an ISO VII environment, as well operating automated, single-use systems for the targeting, expansion and harvesting of cells. The Cell Processing Associate will also collaborate as needed with peers within Manufacturing Sciences and Technology (MST), Quality and Facilities. | 4/27/2023 |
| 4852 | Lyophilization Services of New England Bedford, NH QC Chemist I Bachelor of Science in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study. Exp: 0-3 years |
This position will have responsibility to support various activities in the Quality Control Laboratory. This includes testing the following sample types R&D, in-process, finished product, stability, as well as raw materials. Job duties may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management. | 4/27/2023 |
| 4853 | Marker Therapeutics Houston, TX Cell Therapy Manufacturing Technician BS, MS in Biology or a related science. Exp: 1-5+ years |
Marker Therapeutics is seeking a cell therapy technician for its manufacturing group to support its ongoing efforts to develop immunotherapies for the benefit of patients with cancer. This position will work under the guidance of the Senior Director of CMC and perform assigned responsibilities to support the company’s product manufacturing process and process improvement initiatives. Depending on previous experience and qualifications, this individual will be expected to either lead or support the manufacturing process and process characterization of scale-up/scale-down cell manufacturing processes, including optimizing process parameters, cell concentrations and therapeutic product fill and finish technologies to advance our therapeutic programs. The successful candidate must be a team player with strong expertise in GMP manufacturing and must have the ability to communicate and collaborate within an interdisciplinary environment. | 4/27/2023 |
| 4854 | MatTek Ashland, MA Production Associate I Bachelor’s degree in Biology or equivalent Exp: no previous |
Description: Participates in duties associated with manufacturing of MatTek tissue models according to SOPs where applicable. May also perform duties assigned under Laboratory Assistant as needed. Reporting structure: Works under the direction of more senior Associates and the Laboratory Supervisor/Manager. Reports directly to the Laboratory Supervisor/Manager or Scientist/Senior Scientist. | 4/27/2023 |
| 4855 | Maverick Therapeutics Boston, MA Cell Processing Technician/Specialist Bachelor's degree in biotechnology, biology, engineering or related pharmaceutical science. Exp: 0+ years |
As a Cell Processing Technician/Specialist, working on the Cell Therapy Manufacturing team, you will be empowered to support the manufacturing of Takeda's Cell Therapy products and work with peers to support clean room activities. The main focus of your role will be cGMP cell therapy manufacturing at Takeda's new cell processing facility in Cambridge, Massachusetts. You will directly contribute to the delivery of novel cell products to support human clinical trials. This is an On-Site role.\ | 4/27/2023 |
| 4856 | Maverick Therapeutics San Diego, CA Research Associate II, Global Biologics MS in Molecular Biology, Biochemistry, or related life science. Exp: 0+ years |
At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible to bring life-changing therapies to patients worldwide. Join Takeda as a Research Associate II where you will perform research assignments and be responsible for high-throughput antibody production. You will also work on the discovery and engineering of therapeutic biologics including antibodies, antibody fragments, and fusion proteins. As part of the Biotherapeutic Engineering team, you will report to Scientist II, Biotherapeutic Engineering, where you will interpret and communicate results within the team and with cross-functional project team members. | 4/27/2023 |
| 4857 | Maverick Therapeutics Boston, MA Research Associate II Invitro/Exvivo VD1 Biology MS in a scientific discipline. Exp: 1-2 yrs+ |
The Cell Engager Team of the Oncology Drug Discovery Unit is looking for an enthusiastic lab-based research associate to support the characterisation of antibodies and immune engagers within the Cell Engager portfolio to deliver work packages related to various projects. The work will include the development and running of biological assays to characterise the antibodies, and other biologic entities, the preparation and maintenance of primary and cell line cultures and contribution to the smooth running of the laboratory. The role is laboratory-based within a dynamic cross-functional R&D team. The selected candidate will be expected to conduct routine lab assignmens and protocols; contributes to design of and implementation of improvements for routine procedures | 4/27/2023 |
| 4858 | Merieux NutriSciences Minnetonka, MN Laboratory Technician Bachelor's degree required. Exp: 0+ years |
The incumbent prepares sample for processing and maintains documentation of process to facilitate analysis procedures. | 4/27/2023 |
| 4859 | Merieux NutriSciences Crete, IL Chemist 1 Bachelors preferred. Exp: One - two years |
Analyses w/Extractions (Cholesterol, FAP, ICP, MOJO, FFA, etc.) Ensure that proper analysis methods are conducted on the appropriate samples. Maintain chemistry quality control records and procedures for each test. Extract desired components from samples with appropriate processes such as distillation, solvent extraction and acid digestion, so that concentrations can be determined. Calculate the concentration of components present in samples and post results. Wash glassware as needed and prepare samples as needed. Prepare standards or reagents that are needed for the analysis procedure. Maintain knowledge of Laboratory Information Management System (LIMS) required to complete job responsibilities. Maintain clean laboratory by washing countertops, sweeping floors, storing analysis materials, etc. Initiate and investigate customer complaint and non conformances Determine root cause and corrective action | 4/28/2023 |
| 4860 | Merieux NutriSciences Salt Lake City, UT Chemist 1 Bachelors preferred. Exp: One - two years |
Analyses w/Extractions (Cholesterol, FAP, ICP, MOJO, FFA, etc.) Ensure that proper analysis methods are conducted on the appropriate samples. Maintain chemistry quality control records and procedures for each test. Extract desired components from samples with appropriate processes such as distillation, solvent extraction and acid digestion, so that concentrations can be determined. Calculate the concentration of components present in samples and post results. Wash glassware as needed and prepare samples as needed. Prepare standards or reagents that are needed for the analysis procedure. Maintain knowledge of Laboratory Information Management System (LIMS) required to complete job responsibilities. Maintain clean laboratory by washing countertops, sweeping floors, storing analysis materials, etc. Initiate and investigate customer complaint and non conformances Determine root cause and corrective action | 4/28/2023 |
| 4861 | Merieux NutriSciences Crete, IL Chemist III Masters degree. Exp: 1-2 years |
The incumbent is responsible for performing chemical analysis on food, pharmaceutical, and other sample. The incumbent analyzes the concentration of certain components in food samples. The incumbent must accurately prepare and process the sample to obtain the required results. The incumbent observes daily activities of departmental personnel ranging from receiving to reporting of results and ensures that analysis is performed correctly. The incumbent is responsible for performing chemical analysis on food, pharmaceutical, and other sample. The incumbent analyzes the concentration of certain components in food samples. The incumbent must accurately prepare and process the sample to obtain the required results. The incumbent observes daily activities of departmental personnel ranging from receiving to reporting of results and ensures that analysis is performed correctly. | 4/28/2023 |
| 4862 | Mesa Biotech Florence, SC Analytical R&D Scientist I Bachelor’s degree in chemistry or related field required. Exp: 1-2 years |
The Scientist I conducts laboratory work as necessary to assure that products are tested per operating procedures. Ensure that work is carried out in an efficient and safe manner. Utilizes judgment in making adaptation and modifications on all assignments. Provides routine analyses in an analytical chemistry laboratory following standard practices. Performs analytical methods as assigned for testing on raw materials, samples, stability, production intermediates, and active pharmaceutical ingredients, including method development and qualification activities. Supports internal development and/or manufacturing operations. Makes detailed observations and reviews, documents, and communicates test results | 4/28/2023 |
| 4863 | Mesa Biotech San Francisco, CA Cell Therapy Specialist Bachelor’s or Associates degree in a technical field desired. Exp: 1+ years |
Thermo Fisher Scientific is making a significant investment in the dynamic and rapidly growing Cell Therapy space. Our Cell Therapy organization within the Pharma Services Group, is one of the fastest growing areas of Thermo Fisher Scientific. We focus on providing development and clinical scale services for gene and non-gene modified cell processing for a variety of unmet medical needs. | 4/28/2023 |
| 4864 | Mesa Biotech Middleton, WI Associate Chemist - 2nd Shift Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1+ years |
2nd shift position (2-10pm) Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 4/28/2023 |
| 4865 | Mesa Biotech Middleton, WI Associate Scientist - Bioanalytical Lab Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1+ years |
Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 4/28/2023 |
| 4866 | Mesa Biotech Boston, MA Associate Scientist / Scientist – HPLC , CE Bachelor's degree in Biology, Analytical Chemistry, Biochemistry, Cell & Molecular Biology, Chemical Engineering, or equivalent and relevant formal ac Exp: Associate Scientist: 0-2+ years |
Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. | 4/28/2023 |
| 4867 | Meso Scale Discovery Gaithersburg, MD Research Associate Bachelor’s degree in life sciences, or related area is required. Master’s degree a plus.Bachelor’s degree in life sciences, or related area is require Exp: 1+ years |
This position is responsible for executing experiments and analyzing the resulting data in support of reagent and assay development projects with close supervision. This is a laboratory-based position responsible for advancing research and/or development objectives focused on leading-edge biomarker measurements and technology. · Executes experiments and implements plans under close guidance utilizing established protocols. · Assists in data analysis and the preparation of experimental reports and/or presentations. · Participates in general lab maintenance initiatives including but not limited to maintaining laboratory supplies and equipment, maintaining electronic inventory list database, physical inventory, processing/aliquotting/vialing/labeling materials, and preparing and maintaining reagent inventories. | 4/28/2023 |
| 4868 | Meso Scale Discovery Gaithersburg, MD Research Associate Bachelor’s degree in life sciences, or related area is required. Master’s degree a plus.Bachelor’s degree in life sciences, or related area is require Exp: 1+ years |
This position is responsible for executing experiments and analyzing the resulting data in support of reagent and assay development projects with close supervision. This is a laboratory-based position responsible for advancing research and/or development objectives focused on leading-edge biomarker measurements and technology. · Executes experiments and implements plans under close guidance utilizing established protocols. · Assists in data analysis and the preparation of experimental reports and/or presentations. · Participates in general lab maintenance initiatives including but not limited to maintaining laboratory supplies and equipment, maintaining electronic inventory list database, physical inventory, processing/aliquotting/vialing/labeling materials, and preparing and maintaining reagent inventories. | 4/28/2023 |
| 4869 | Meso Scale Discovery Rockville, MD Engineer I, Process Bachelor’s degree in chemical/biochemical engineering or related field. Exp: one year |
Responsible for developing, characterizing and validating manufacturing processes to produce biochemical assay plates and related consumables. | 4/28/2023 |
| 4870 | Meso Scale Discovery Gaithersburg, MD Cell Culture Specialist I Bachelor's degree in Biology, Chemistry, Biotechnology, Engineering or a related field. Exp: six months |
This position is responsible for the production of cell-based products including but not limited to hybridoma antibodies and recombinant antibodies. | 4/28/2023 |
| 4871 | Meso Scale Discovery Gaithersburg, MD Research Associate Bachelor’s degree in life sciences, or related area is required. Master’s degree a plus. Exp: 1+ years |
This position is responsible for executing experiments and analyzing the resulting data in support of reagent and assay development projects with close supervision. This is a laboratory-based position responsible for advancing research and/or development objectives focused on leading-edge biomarker measurements and technology. · | 4/28/2023 |
| 4872 | Metabolon Morrisville, NC Medical Lab Scientist 1 BS degree in a life science. Exp: 0-2 years |
Due to our rapidly growing services business, Metabolon is seeking a Medical Laboratory Scientist to work within the Platform Analysis group as an integral member of our Global Metabolomics Services team. The team member in this position will be responsible for all aspects of routine laboratory testing using our liquid chromatography–mass spectrometry (LC-MS) based instrumentation. The ideal candidate will have experience in LC-MS and will be expected to contribute to continuous improvement initiatives as required. In addition, the candidate will have a successful laboratory performance track record contributing as a team player in high throughput clinical laboratory testing environment. | 4/28/2023 |
| 4873 | Microbiologics Saint Cloud, MN Production Innovation Lab Technician, Saint Cloud Four (4) year degree in relevant field (e.g., biology, microbiology, virology, cell biology, molecular biology, food science). Exp: 1-year |
We are currently looking to add a Production Innovation Lab Technician to our team in St. Cloud, MN. In this role you will Assist with supervised experiments using microbiology techniques as well as other applicable methodologies leading to new products or process improvements. Generally required to apply education and work experience to conduct focused research thoughtfully, collaboratively, and efficiently with high integrity. | 4/28/2023 |
| 4874 | Microbiologics Saint Cloud, MN Quality Control Lab Technician, Saint Cloud Four-year microbiology or related degree required. Exp: 1+ years |
We are currently looking to add a Quality Control Lab Technician to our St. Cloud, MN team. In this role, you will perform Quality Control Testing, Shelf-Life Testing, and Packaging Event Evaluations on Microbiologics products in accordance with the appropriate Company Device Master Record (DMR), policies and procedures with the objective to release only production products that meet all of Microbiologics acceptance criteria. | 4/28/2023 |
| 4875 | Mirus Bio Madison, WI Laboratory Technician - Temporary College courses related to Biology and Chemistry preferred. Exp: 1+ years’ |
We are seeking a full time Laboratory Technician with an interest in biotechnology to perform general laboratory support duties, equipment maintenance, dispensing reagents, and labeling vials/bottles. This position will report to the Production Supervisor, and work closely with Quality, Shipping and R&D departments. | 4/28/2023 |
| 4876 | Moderna Therapeutics Norwood, MA Engineer I, Process Development BS or MS in chemical engineering, biological engineering, chemistry, biochemistry, or closely related field. Exp: 0-2 years |
This role will support the development of manufacturing processes for Moderna’s mRNA-based medicines to enable clinical and commercial supply, with a focus on process understanding and process control strategy definition, and the optimization, transfer, and characterization of manufacturing processes. The role will additionally interface with and support cross-functional teams across CMC, Research and Development, Pre-clinical and Clinical Manufacturing, Quality, and Analytical Development. Applicants must have demonstrated experience in designing, executing, and analyzing scientific experiments. Relevant academic and/or industrial experience in drug substance or drug formulation/delivery development is ideal. Previous experience with chromatography, nanoparticle formulations, filtration technologies, mixing technologies, and/or statistical design of experiments is preferred. | 4/28/2023 |
| 4877 | Moderna Therapeutics Norwood, MA Manufacturing Associate I Requires BA/BS in a relevant science or engineering discipline. Exp: 1+ years |
Moderna is seeking a highly driven individual for a Manufacturing Associate I position within High Throughput Operations (HTOps), at the Moderna manufacturing site in Norwood, MA. The HTOps team is responsible for high throughput production of mRNA and LNP in support of Moderna’s research portfolio. This position is Monday-Friday 7am-3pm shift. The individual hired into this role will independently execute DNA, RNA, and/or LNP unit operations following standard operating procedures. This individual is expected to be detail oriented and adhere to good laboratory practices, with a goal of manufacturing high quality DNA, RNA and LNP. In addition to daily production, the Manufacturing Associate I will be responsible for escalating issues experienced while processing. They are expected to take the initiative to learn the science behind the process that is being run, to fundamentally understand the process steps. The Manufacturing Associate I is expected to have a team mentality and respects the common work areas. They help to maintain the cleanliness, and 5S initiatives put into place in the lab in common areas as well as unit assigned areas. Commitment and active participation in the safety culture is required. In addition to a focus on manufacturing and maintaining the lab, it is strongly desired that the individual actively participates in the department’s continuous improvement and optimization initiatives. The successful candidate must demonstrate the ability to quickly master new processes and have the drive to be part of a dynamic, fast paced, and highly engaged and motivated team. | 4/28/2023 |
| 4878 | Moderna Therapeutics Norwood, MA Research Associate, Nucleic Acid, Process Development BS or MS in Chemical or Biochemical Engineering, Biology, Biochemistry, or closely related field. Exp: up to 3 years |
Moderna is working to develop first-in-class messenger RNA (mRNA) based medicines. DNA Process Development, a team residing in Moderna’s Technical Development organization, has been tasked with development and implementation of processes to produce DNA and enzymes utilized in the production of RNA. Our efforts in this area are growing, and Moderna is seeking a new team member to join the DNA Process Development team for a position based at the Norwood, MA site. In this role, you will have the opportunity to help develop new processes to facilitate rapid DNA and mRNA production at Moderna, with a focus on applying state of the art molecular biology and automation technologies. The incumbent will collaborate closely with the nucleic acid process development and process automation teams to develop new technologies for application in plasmid DNA manufacturing. Our goal is to enable clinical studies and to support commercial manufacturing, so you will work closely with multiple functions spanning development, technical operations and manufacturing. | 4/28/2023 |
| 4879 | Fresenius Kabi Melrose Park, IL Scientist I Bachelor of Science in Chemistry, Biology or related physical science. Exp: 1+ years |
A Scientist I in Quality Control is responsible for an intermediate level of expertise in analytical chemistry, chromatographic methods of analysis and instrumentation, including troubleshooting. Directs and provides guidance to associate scientists. | 4/18/2023 |
| 4880 | Fresenius Kabi Melrose Park, IL Scientist I Bachelor of Science in Chemistry, Biology or related physical science. Exp: 1+ years |
A Scientist I in Quality Control is responsible for an intermediate level of expertise in analytical chemistry, chromatographic methods of analysis and instrumentation, including troubleshooting. Directs and provides guidance to associate scientists. | 4/18/2023 |
| 4881 | Fresenius Kabi Grand Island, NY ASSOCIATE SCIENTIST - 2nd Shift Chemistry Possess a B.S. in Chemistry, Biology, or related physical science. Exp: 0-2 years |
An Associate Scientist is responsible for performing entry level chemical testing to support raw material, in-process, stability, and finished products as required for Quality Control. Effectively communicates work and results both orally and in writing. | 4/18/2023 |
| 4882 | Fresenius Kabi Melrose Park, IL Manufacturing Engineer Bachelor’s degree in Engineering (Electrical, Chemical, Controls, Computer, Mechanical, etc.). Exp: 1-3 years |
Responsibilities include using technical expertise in support of daily operations in aseptic filling or formulation by defining, measuring, analyzing, coordinating, implementing and follow-up concerning projects and activities designed to increase or improve safety, quality, productivity, and/or capacity. Apply accepted engineering practices and project management techniques to assigned daily tasks and projects. Analyze situations, break them down into key components and milestones, conduct fact-finding missions, provide detailed plans of action, and implement plans as assigned. | 4/18/2023 |
| 4883 | Fresenius Kabi Grand Island, NY ASSOCIATE SCIENTIST - 1st Shift Chemistry Possess a B.S. in Chemistry, Biology, or related physical science. Exp: 0-2 years |
An Associate Scientist is responsible for performing entry level chemical testing to support raw material, in-process, stability, and finished products as required for Quality Control. Effectively communicates work and results both orally and in writing. | 4/18/2023 |
| 4884 | Fresenius Kabi Wilson, NC MQA SPECIALIST II (NIGHTS) Bachelor of Science degree Exp: 1-3 years |
Performs routine audits of manufacturing areas to ensure product quality and SOP/GMP compliance at the Wilson Manufacturing Facility. Assists in troubleshooting manufacturing problems and inspection defects. Provides plant support for collection of data where needed, while assembling required metrics for review by facility management. Updates controlled documents, including SOPs, policies and batch records to maintain compliance in the production areas. | 4/18/2023 |
| 4885 | Galatea Surgical Research Triangle Park, NC Senior Scientist (Onsite - Durham, NC Research Triangle Park) Graduate degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, Materials Science & Engineering, Polymer Science, Textiles or related fie Exp: 0-5 years |
The incumbent will carry out experimental studies relating to drug/device combination technology within the Interventional Innovation R&D team at BD Technologies and Innovation (BDTI) with an initial focus on BD’s Interventional business segment. Specifically, the candidate will guide in drug formulation and delivery technologies, soft materials characterization, and drug-biomaterials-tissue interactions. They will work with project team members to plan and implement technical assessments of coatings for medical devices and drug delivery technologies/products. Additional areas for technical assessment may be included as well, for example, biocompatible implants and materials for use in surgical procedures. They will be responsible for the execution of technical work and communication of results to various collaborators. Additional responsibilities include investigating and resolving technical problems and managing different workstreams to meet program objectives and timelines. The candidate will author/review SOPs, test/project reports, and other documents as required to implement studies in the laboratory. The incumbent is expected to work closely with other R&D project team members and support functions within BDTI and BD business units, contribute intellectual property, create experimental designs/test methods, and analyze experimental data. They will work with project team leadership to help ensure a smooth transition of projects from the Innovation phase to product development. | 4/18/2023 |
| 4886 | DVC LLC Atlanta, GA Scientist - Laboratory and Specimen Management MS in Microbiology or Biology Exp: 0-2 years |
GDIT is currently seeking a Scientist with microbiology background supporting research, diagnostics, and surveillance activities for a team focused on influenza pandemic preparedness for the CDC in Atlanta GA.This role may be required to perform preparation, culture, and characterization of viral or bacterial strains or mammalian cell lines using a wide range of techniques and approaches. You will assist in maintenance of laboratory supplies and reagents including ordering, receiving, stock preparation and validation of reagents, solutions, and standards prior to use. The desired candidate will be able to work well with a diverse workforce within the Immunology and Pathogenesis Branch (IPB) as well as other branches in Influenza Division.This position is located on the Roybal Campus in Atlanta, Georgia. | 4/18/2023 |
| 4887 | GenScript Pisctaway, NJ Research Scientist – Automated Process Development MS in Biology/ Biochemistry/ Molecular Biology/ Biomedical Instrumentation/ Bioengineering Discipline or related subjects. Exp: 1 year |
We are looking for a Research Scientist – Automated Process Development to support the key high throughput molecular biology reagent production needs in the US Molecular Biology/ Reagent services business unit. | 4/18/2023 |
| 4888 | Glaukos San Clemente, CA MANUFACTURING TECHNICIAN II - PHARMA OPERATIONS bachelor’s degree in science or engineering Exp: 0 – 2 years’ |
The Manufacturing Technician II, based in San Clemente, CA, will perform all activities with good documentation practices (GDP) in accordance with current good manufacturing practices (cGMPs) and quality system regulation (QSR) medical device good manufacturing practices (GMP) requirements. | 4/18/2023 |
| 4889 | Grand River Aseptic Manufacturing Grand Rapids, MI QC Microbiology Technician (2nd or 3rd shift) Bachelor’s degree in microbiology or a related field Exp: 0-2 years’ |
The Microbiology Technician supports quality control and assurance by assisting the microbiology department with environmental monitoring, water testing, and client specific testing. | 4/19/2023 |
| 4890 | Grand River Aseptic Manufacturing Grand Rapids, MI QC Chemist - 3rd Shift Bachelor’s degree in Chemistry and/or other related discipline (e.g. Biochemistry, Biotechnology). Exp: 1 years |
The QC Chemist supports quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties include, but are not limited to, providing general laboratory support for raw material, in-process, stability, and finished product testing. | 4/19/2023 |
| 4891 | Greenlight Biosciences Lexington, MA Biomanufacturing Associate BS/BA in Biotechnology, Microbiology, Cell Biology, Chemical Engineering, Biochemistry or equivalent Exp: 0+ years |
We are seeking a Biomanufacturing Associate for a manufacturing role to start-up and run day to day operation of GreenLight’s cGMP manufacturing operations in Lexington, MA. This individual will initially assist in the installation and qualification of biomanufacturing equipment leading into the production GMP materials in support of GreenLight’s portfolio. They will be tasked with being part of a dynamic manufacturing team scaling up and producing RNA material under GMP conditions in support of Clinical operation. The position offers growth potential for a very experienced manufacturing associate or someone just starting off their Biotech career with a growing biomanufacturing team within a growing company. | 4/19/2023 |
| 4892 | GRO Biosciences Cambridge, MA RA/Senior RA, Application Sciences MS degree or BS/BA degree in biology, microbiology, biochemistry, biotechnology, synthetic biology, systems biology, biological engineering, or relate Exp: BS: 1 year |
GRO Biosciences (GRObio) is hiring a Research Associate (RA) or Senior RA to develop novel protein therapies produced from the company’s recoded organism platform. Recoded organisms bear an expanded genetic code and enable GRObio to generate revolutionary products of unprecedented structural and chemical diversity. With the tools at GRObio, you’ll be able to propose, develop, and implement completely differentiated solutions to longstanding, critical problems. GRObio is seeking a motivated team-player and problem-solver to contribute to preclinical product development within Application Sciences. Ideal candidates thrive in new areas, can “wear many hats”, and will enjoy an outsized impact on the growth of an early-stage company. Regular activities will include planning and carrying out experiments throughout our pipeline, including strain development, biomass generation, protein purification, protein characterization, and bioassays. This position will interface heavily with team members from other groups, including collaborations with automated R&D divisions to realize rich datasets. There is substantial growth opportunity within the company for the capable candidate. | 4/20/2023 |
| 4893 | HelixBind Boxborough, MA Formulation Technologist Certificate, Associate’s or Bachelor’s degree in a science or engineering discipline. Exp: 0-5 years’ |
We are seeking a talented and motivated individual to join our R&D Team as a Formulation Technologist. This is a great time to join our team. The position offers the exciting opportunity to grow along with the Company as we take our initial product through FDA clearance and market launch while, in parallel, build out our pipeline of impactful syndromic diagnostic assays. | 4/20/2023 |
| 4894 | Heska Des Moines, IA Technician I, II or III, Bacterins Bachelor’s Degree in a science or bio-technology field. Exp: Technician I: 1 year |
The Bacterins Technician I position will work under the close supervision of the Bacterins supervisor to foster the growth of bacterial cultures through fermentation and cell media preparation while maintaining a sterile environment. This position requires the ability to multi-task and follow standard operating procedures. Technican level will be based on revelant experience. | 4/21/2023 |
| 4895 | i2O Therapeutics Cambridge, MA Research Associate (in vivo) AA/AS/BA/BS in a science field Exp: 1 year |
i2o Therapeutics is a biotech startup developing a drug delivery platform to convert injectable therapies into oral modalities. This full-time, hourly position includes conducting and assisting with in vivo studies to support a variety of projects within a small, multi-functional team | 4/21/2023 |
| 4896 | Integrated DNA Technologies Coralville, IA Research Scientist II-Enzyme Development Master’s degree (in Biology, Genetics, Chemistry or a related life sciences field). Exp: one or more years |
The Research Scientist II, under minimal direction, conducts bench scientific experimentation that advances the basic science of nucleic acids and nucleic acid biochemistry and assists with the development and characterization of new IDT protein products in the CRISPR, qPCR, and NGS domains. This position is responsible for planning and executing experiments, analyzing data, and reporting/presenting findings as well as supporting IDT customers. A background in bacterial genetics and/or protein engineering is highly preferred. This position is equivalent to a Research Assistant II position at an academic institution. | 4/21/2023 |
| 4897 | Integrated DNA Technologies Danvers, MA Research Associate BSc or BA in a Scientific discipline Exp: 1 to 4 Years |
Research Associates are responsible for the undertaking of research and development activities to support contracted pharma projects to develop companion diagnostics IVDs. The Research Associate will be responsible for performing required laboratory studies, including making observations, reporting data and providing results to support key decisions within the Pharma Partnerships business unit. A shown ability to communicate (verbal and written) and work with all levels of staff is fundamental to this role. Ensure all work is conducted in accordance with applicable protocols and work instructions and that all work is appropriately documented per procedure. | 4/21/2023 |
| 4898 | Inova Diagnostics Orangeburg, NY BioReagent Technologist I BS in a Science field or related technical discipline Exp: up to two years |
Responsible for the isolation and purification of proteins from recombinant and natural sources. | 4/21/2023 |
| 4899 | Inova Diagnostics Orangeburg, NY BioReagent Technologist I BS in a Science field or related technical discipline Exp: up to two years |
Responsible for the isolation and purification of proteins from recombinant and natural sources. | 4/21/2023 |
| 4900 | Inova Diagnostics San Diego, CA Chemist IFA Slides - AID Bachelor's degree (B.A.) or (B.S.) in the biological, chemical or related sciences Exp: 0-1 years |
The IFA Slides department is looking for a candidate to be apart of a fast-paced, supportive manufacturing team to assist with preparation of autoimmune diagnostic Immunofluorescence Assays (IFA) cell culture slide products. Opportunites for advancement and career growth while performing, mammalian cell culture, immunofluorescence cell suspension and slide preparation activities. | 4/21/2023 |
| 4901 | Inscripta Pleasanton, CA Research Assistant/Research Associate I, Synbio Bachelor’s degree in a scientific discipline or associate degree from a laboratory science or biotechnology program will be considered. Exp: 1+ year |
The Research Assistant/Research Associate I will primarily assist in lab management services such as media preparation, inventory, and shipping & receiving activities. They will report directly to the Laboratory Manager but will have opportunities to cross train and support other groups such as Screening, Analytic Chemistry, and Strain Banking. The successful candidate will be a team player who works within the group to meet department goals, objectives, and tasks to achieve desired results. They can respond to new requests with appropriate urgency and an organized approach and hold themselves accountable to fulfill assigned tasks and achieve results within assigned timelines. | 4/21/2023 |
| 4902 | Integral Molecular Philadelphia, PA Research Associate - (Job ID# 04182023) Bachelor’s degree in biology, bioengineering, or a related field Exp: 1–2 years |
Our close-knit, medium-sized company is composed of smart, curious, diverse scientists who take an active interest in the scientific and technical development of our team members. We seek a Research Associate I to join our dedicated group of scientists. A desirable candidate will have the skills to culture mammalian and/or bacterial cells, perform DNA mini-preps, and complete bacterial transformations and cell transfections. Familiarity with flow cytometry is an added bonus! | 4/21/2023 |
| 4903 | Iovance Biotherapeutics Philadelphia, PA Quality Control Analyst I, Lab Support [Contract to Hire] Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Exp: 1 year |
Iovance Biotherapeutics is a growing, late-stage company focused on the development and commercialization of novel cancer immunotherapies. Iovance is seeking a Quality Control (QC) Laboratory Support Analyst I who will assist the Laboratory Manager with the day-to-day upkeep of the QC laboratories including but not limited to collecting data for trending, maintaining positive control inventories for various QC assays, and uploading assay records to the document management system. The ideal candidate will have experience working in a GMP-regulated laboratory with pipetting knowledge but is not required. The position will report to the Lab Support Manager, Quality Control. | 4/21/2023 |
| 4904 | Iovance Biotherapeutics Philadelphia, PA Quality Control Analyst, Microbiology (Weekend shift) [Contract to Hire] Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Exp: one (1) year |
The Quality Control Analyst will support quality control testing operations at Iovance’s Cell Therapy Center (iCTC). The quality control testing programs include in-process and final drug product microbial testing such as bioburden, endotoxin, gram stain, environmental monitoring, and sterility techniques. This position will work a weekend shift (10 hr shifts Wed-Sat) to support manufacturing weekend activities. | 4/21/2023 |
| 4905 | iRhythm Technologies Cypress, CA Manufacturing Engineer II Bachelor’s Degree in Engineering or a related field required Exp: 1-3 years |
iRhythm Technologies has an opening for a full-time technical expert in manufacturing engineering. The Senior Manufacturing Engineer will provide manufacturing support for existing products and processes as well as new products, product changes, line extensions and enhancements including all associated equipment validation. In this dynamic environment you will have the opportunity to develop your technical skills and leadership competencies in the MedTech and wearable device industry while advancing your career. Our work environment is fast paced, with a collaborative atmosphere. Most of all, we are passionate about delivering innovations that improve the quality of health care and the patient experience. We are looking for like-minded individuals to join our team today! | 4/21/2023 |
| 4906 | Cambridge Isotope Laboratories Xenia, OH Quality Assurance Associate Bachelor’s Degree in chemistry or related science preferred Exp: 0-2 years |
Cambridge Isotope Separations (CIS) is searching for a GMP Quality Assurance (QA) Associate located in Xenia, Ohio. CIS is the world leader in the separation of stable isotopes and related chemistry. CIS and its parent, Cambridge Isotope Laboratories (CIL) in Massachusetts, are subsidiaries of the Otsuka Pharmaceutical Group. CIL separates both 13C and 18O at its Xenia, Ohio, facility and operates the only large capacity nongovernmental Deuterium Oxide enrichment columns in the world. We globally support a broad range of customers across many high-tech industries including pharmaceutical, semiconductor, medical diagnostic, display, and basic research. We are rapidly expanding, and the Ohio facility is an integral part of our growth for the future. Under general supervision, the primary responsibility of the QA Associate is to work as a team member to ensure and maintain the Company’s cGMP (Current Good Manufacturing Practices) compliance. | 4/21/2023 |
| 4907 | Cambridge Isotope Laboratories Andover, MA Quality Control Analyst I BS or MS degree in Chemistry, Chemistry Informatics or other relevant science degree, or relevant experience that will substitute for a formal degree Exp: One or more years |
Cambridge Isotope Laboratories, Inc. (CIL) is seeking a Quality Control Analyst I to join our team based onsite in our Andover, MA location. As the leading company in a niche scientific market, CIL works with cutting edge researchers in clinical diagnostics, metabolic research, proteomics, environmental testing, protein discovery, drug development, metabolomics, and industrial research. CIL's growing customer base spans academia, pharmaceutical and industry, enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. The Quality Control (QC) Analyst I is responsible for conducting routine analysis of materials under general supervision and in accordance with standard operating procedures (SOPs). The analyst will compile data for documentation of test procedures and prepare reports. They will also calibrate and maintain lab equipment. Some travel may be required to our Tewksbury, MA facility. | 4/21/2023 |
| 4908 | Janssen Pharmaceuticals San Diego, CA Neuropsychiatry Research Associate master’s degree in a relevant field Exp: 1 year |
Janssen R&D La Jolla, a member of Johnson & Johnson's Family of Companies, is recruiting a Research Associate in Neuroscience drug discovery, located in San Diego, CA. | 4/21/2023 |
| 4909 | Jnana Therapeutics Boston, MA Research Associate/Senior Research Associate, Chemical Biology BS or MS in Biology or other relevant area. Exp: 1-2 years |
Jnana Therapeutics is seeking an enthusiastic and highly motivated Research Associate/Senior Research Associate to work in our multidisciplinary Chemical Biology group. Using our novel hit generation platform and a range of cell-based assays, our research aims to unlock difficult to drug targets and ultimately small molecules that modulate these proteins. Prior experience in drug discovery is preferred. Strong commitment and good work ethic are essential. | 4/21/2023 |
| 4910 | JRF Global Audubon, PA Scientist I / Entry Level Chemist Bachelor of Science or advanced degree from an accredited college or university in chemistry or other science-related field. Exp: 1-3 years |
Set up experiments under the guidance of a Scientist II and/or Team Lead Operate equipment, observe and log the progress of experiments Promptly submit experimental data / findings to the supervisor Promptly inform the supervisor of any problems encountered during the experiments. Assist in data entry in various formats and verify accuracy of data entry Assist in writing drafts of Protocols and Reports Provide a daily update on the progress, findings and results for each experiment. Compile the data as directed by the supervisor Check the quality and accuracy of the data before submission to the supervisor | 4/21/2023 |
| 4911 | J-Star Cranbury, NJ Research Chemist Master’s Degree in Chemistry or Chemical Engineering Exp: one year |
Develop analytical methods to separate, detect, and analyze Active Pharmaceutical Ingredient (API), intermediates, impurities, starting material and excipients from drug substances and drug products. Analyze organic and inorganic compounds to determine chemical or physical properties, composition, structure, relationships, reactions, using chromatography, spectroscopy, spectrophotometry techniques including HPLC, UPLC, IC, GC, MS, UV, PXRD, DSC, TGA, NMR, and KF. Design and perform method verification and validation. Determine the specificity, linearity, accuracy, precision, forced degradation, robustness of the methods. | 4/21/2023 |
| 4912 | J-Star Cranbury, NJ Analytical Research Scientist II/III (DPD) MS in Chemistry, Pharmaceutical Science or related field. Exp: 1 -3 years |
The primary responsibility in this role is to perform analytical testing of drug substance, intermediates, drug product in support of J-Star’s drug product development projects. The incumbent should provide the expertise in characterization of drug product formulation using HPLC, GC, DSC, TGA, XRPD, dissolution apparatus, particle size analyzer, Karl Fischer titrator. Specifically, the incumbent will be responsible for analysis of formulations from preclinical through clinical formulation development, of oral solids, liquids, injectables and semi-solid dosage forms for new drug candidates. | 4/21/2023 |
| 4913 | J-Star Cranbury, NJ Research Chemist MS degree in Chemistry, Chemical Engineering or related field. Exp: 6 months |
Must have knowledge of API processing, Crystallization, Chromatography, Distillation. perform API crystallization process in compliance with cGMP and FDA regulations, utilizing analytical tools including chromatography, separation, and solvent selection; support crystallization process development by conducting studies involving compound properties and experimental conditions; participate in the scale-up development of enabling technology and experiments to facilitate the co-processing and development of API; conduct routine stability, performance, and evaluation studies for solid state characterization and pre-formulation support; support early drug crystallization process development for high potency compounds and controlled substance; purify pharmaceutical compounds using column chromatography, crystallization, trituration, extraction, and distillation; utilize experimental and simulation/modeling approaches to perform solvent selection and solve process challenges arisen from scale-up crystallization process; collect, analyze and maintain data integrity under Good Documentation Practice; write/review developmental chemistry, process optimization and process scale-up reports to support FDA requirements for CMC (Chemistry, Manufacturing and Control) sections of INDs/NDAs. | 4/21/2023 |
| 4914 | KBI Biopharma Durham, NC Upstream Process Development Associate I/II Bachelor’s in Chemical Engineering, Biotechnology or related area. Exp: 1-3+ years’ |
KBI Biopharma seeks to fill a role for Upstream Cell Culture Process Development Associate. This person will lead and assist in cell culture and harvest projects for mammalian cell lines (mainly CHO variants) in support of process development, scale-up, and technology transfer to cGMP manufacturing. | 4/21/2023 |
| 4915 | KBI Biopharma Boulder, CO Manufacturing Associate I/II (Nights) Bachelor’s degree Exp: 0-5 years |
This position will be on a 4-3 night shift schedule. The hours are 7:00 pm to 7:00 am. Coordinate and perform cGMP manufacturing operations for manufacturing biopharmaceutical products. Ensure the effective use of material, equipment, and personnel while making products at high-quality levels | 4/21/2023 |
| 4916 | KBI Biopharma Boulder, CO Manufacturing Associate I/II (Nights) Bachelor’s degree Exp: 0-5 years |
This position will be on a 2-2-3 night shift schedule. The hours are 7:00 pm to 7:00 am. Coordinate and perform cGMP manufacturing operations for manufacturing biopharmaceutical products. Ensure the effective use of material, equipment, and personnel while making products at high-quality levels | 4/21/2023 |
| 4917 | KBI Biopharma Durham, NC Downstream Process Development Associate I/II or Senior For PD Associate I: B.S. degree in biotechnology or related area; For PD Associate II: M.S. degree (industrial experience a plus). Exp: B.S.: 0-2+ years’; M.S.: 0-2+years’ |
Responsible for supporting process development activities for downstream production processes, instruments, and equipment. | 4/21/2023 |
| 4918 | KBI Biopharma Durham, NC Research Associate I/II For RA I: Bachelor’s degree in chemistry, biochemistry or related area; For RA II: Master’s degree in chemistry, biochemistry or related area. Exp: RA I: 0+ years’; RA II: 0+ years’ |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. | 4/21/2023 |
| 4919 | Dropworks Hercules, CA Production Chemist I - Temporary - $1,500 Hiring Bonus Bachelor’s degree in a life science or related field. Exp: 1-3 years |
Contribute to our mission of improving the quality of life for millions by contributing to the production of life science products our customers use to advance healthcare. Help build high quality products following detailed processes and procedures to ensure the integrity of our products. | 4/9/2023 |
| 4920 | Dr. Reddy's Laboratories Middleburgh, NY Associate Quality Bachelor’s Degree in Chemistry or Biochemistry is normally required. Exp: 0-3 year's |
We seek a dynamic Quality Associate to join our fast-paced environment at our Manufacturing site in Middleburgh, NY | 4/9/2023 |
| 4921 | EAG Laboratories Minneapolis, MN Laboratory Technologist l Bachelor’s degree in a chemical, physical, biological or clinical laboratory science, or medical technology from an accredited institution. Exp: 1-3 years |
Technologist I responsibilities include, but are not limited to, the following: Following prescribed procedureswhile performing serology testing on donor plasma and serum including EIA, PCR, and ABO blood typing. Calculating the results of the tests performed as necessary Operating, calibrating, conducting performance checks, and maintaining laboratory analyzers and equipment Recognizing and correcting basic analyzer malfunctions. Notifying management personnel when appropriate Preparing reagents or media from a prescribed procedure Evaluating media, reagents, and calibrators according to established criteria Conducting established quality control procedures on analytical tests, equipment, reagents, media, and products Evaluating results of quality control and implementing corrective action when indicated Determining performance specifications for new methods Confirming and verifying results through knowledge of techniques, principles, and analyzers Monitoring quality assurance/continuous improvement programs | 4/9/2023 |
| 4922 | EAG Laboratories Minneapolis, MN Technologist l (3rd Shift) Bachelor’s degree in a chemical, physical, biological or clinical laboratory science, or medical technology from an accredited institution. Exp: 1-3 years |
Technologist I responsibilities include, but are not limited to, the following: Following prescribed procedures while performing serology testing on donor plasma and serum including EIA, PCR, and ABO blood typing. Calculating the results of the tests performed as necessary Operating, calibrating, conducting performance checks, and maintaining laboratory analyzers and equipment Recognizing and correcting basic analyzer malfunctions. Notifying management personnel when appropriate Preparing reagents or media from a prescribed procedure Evaluating media, reagents, and calibrators according to established criteria Conducting established quality control procedures on analytical tests, equipment, reagents, media, and products Evaluating results of quality control and implementing corrective action when indicated Determining performance specifications for new methods | 4/9/2023 |
| 4923 | EAG Laboratories St. Louis, MO Laboratory Technician (Analytical Chemistry) - EAG Laboratories - St. Louis, MO BS degree in Chemistry. Exp: 1-3 years |
EAG is actively seeking a Lab Technician to support Analyst and Scientist in the formulation of industrial and consumer products. In this position, you will be responsible for: Performing sample preparation. Assist with recording test data providing some basic analysis and interpretations. Maintaining specified records of scientific data. Protecting confidential information and proprietary processes. Handling customer materials and company equipment in a responsible and efficient manner. | 4/9/2023 |
| 4924 | EAG Laboratories St. Louis, MO Analyst, Analytical Chemistry - EAG Laboratories MS degree in Chemistry. Exp: 0-2 years |
EAG is actively seeking a chemist to assist in the formulation of industrial and consumer products. In this position, you will be responsible for: Applying standard and non-standard techniques, procedures and criteria to carry out a sequence of related tasks to determine the composition, properties and/or structure of materials. Performing sample preparation. Recording test data providing some basic analysis and interpretations. Maintaining specified records of scientific data. Preparing reports on analytical results for customers. Protecting confidential information and proprietary processes. Handling customer materials and company equipment in a responsible and efficient manner. | 4/9/2023 |
| 4925 | EAG Laboratories Phoenix, AZ Bacteriology / Biochemistry Analyst - Eurofins EmLabs Bachelor’s degree in microbiology, molecular biology, biochemistry or a closely related science. REQUIRED Exp: 1-2 years |
The Analyst performs bacteriological and molecular/biochemical analysis on samples including but not limited to aerobiological, environmental and drinking water. The Analyst prepares and analyzes environmental samples according to scientific methodology in compliance with company Quality Assurance programs and SOP’s, and must be knowledgeable of both job-specific routine and complex analyses. The analyst validates and reviews data for accuracy, and uploads laboratory data into the LIMS that ultimately generates required reports to clients. Schedules sample workload according to due dates and sample hold times, and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation. | 4/10/2023 |
| 4926 | EAG Laboratories Phoenix, AZ Analyst I - Eurofins Built Environment - Phoenix, AZ BS or BA in a closely related science. Exp: 1-2 years |
Eurofins Built Environment Testing is searching for a Fungal Analyst in Phoenix, AZ. The Analyst prepares and analyzes environmental samples according to scientific methodology in compliance with company Quality Assurance programs and SOP’s, and must be knowledgeable of both job-specific routine and complex analyses. The analyst validates and reviews data for accuracy, and uploads laboratory data into the LIMS that ultimately generates required reports to clients. Schedules sample workload according to due dates and sample hold times, and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation | 4/10/2023 |
| 4927 | Exponential Business & Technologies Eden Prarie, MN Nano Analytical and Testing Lab Technician BE or BS degree in Materials Science and Engineering, Mechanical Engineering, Physics, Chemistry or related disciplines. Exp: One to two years |
Ebatco is seeking an energetic, self-disciplined, customer service oriented technical person to join its Nano Analytical and Testing Laboratory (NAT Lab). As a technical member of the NAT Lab team, the technician performs contract lab services and instrument demonstrations with appropriate levels of support and supervision, operates advanced nano/micro scale scientific instruments, collects testing and measurement data, and writes technical report on experimental results and observations. | 4/10/2023 |
| 4928 | Elektrofi Boston, MA Analytical Development - Associate Scientist Bachelor's or Master's degree in Microbiology or a related field. Exp: 0-2 years |
Elektrofi is seeking a highly motivated and detail-oriented Associate Scientist who will be responsible for developing, qualifying and performing microbiological and sterility assays for release testing our drug products. This individual will join a multidisciplinary team of scientists and engineers and contribute to a variety of CMC activities in a highly collaborative environment. | 4/10/2023 |
| 4929 | Elektrofi Boston, MA Formulation Development - Associate Scientist BS in Pharmaceutical Sciences, Chemical Engineering, Chemistry, Biology, Bioengineering, or a related field. Exp: 0-2 years |
Elektrofi is looking for an Associate Scientist to support a team responsible for the development of platform formulations for Elektrofi’s proprietary microparticle production process. The candidate will support ongoing activities towards the development of Elektrofi’s biologics formulation platform. This individual will join an early-stage, multidisciplinary team of scientists and contribute to a variety of formulations activities in a highly collaborative environment. | 4/10/2023 |
| 4930 | Elektrofi Boston, MA Internal Manufacturing - Engineer I/II B.S. in Mechanical, Chemical, Biomedical, or Materials Engineering, Chemistry, Physics, or a related engineering discipline. Exp: up to 2 years’ |
Elektrofi is looking for an Engineer I/II to support manufacturing, process development, or drug product development in the manufacturing and analysis of biologically active microparticle suspensions and their interactions with delivery devices. This individual will join a growing, multidisciplinary team of scientists and engineers and contribute to a variety of manufacturing and process development activities in a highly collaborative environment. | 4/10/2023 |
| 4931 | Elektrofi Boston, MA Analytical Development - Associate Scientist Bachelor's or Master's degree in Microbiology or a related field. Exp: 0-2 years |
Elektrofi is seeking a highly motivated and detail-oriented Associate Scientist who will be responsible for developing, qualifying and performing microbiological and sterility assays for release testing our drug products. This individual will join a multidisciplinary team of scientists and engineers and contribute to a variety of CMC activities in a highly collaborative environment. | 4/10/2023 |
| 4932 | Elektrofi FLOOR 2, MA Drug Product Innovation - Associate Scientist/Engineer BS Degree in Chemical, Biomedical, Materials, or Pharmaceutical Engineering, or Colloid Science or relevant discipline. Preference for MS in relevant Exp: 0-3 years’ |
Elektrofi is looking for an Associate Scientist or Engineer I to support the Drug Product Innovation team and investigate Elektrofi’ s microparticle suspensions. This work includes phase appropriate container selection, determination of microparticle and suspension critical quality attributes (CQAs), optimization of resuspendability and injectability, fill-finish development, as well as the development of new embodiments of the product across a range of applications. An exciting opportunity to join a multidisciplinary team of scientists and engineers and contribute to a variety of research and development activities in a highly collaborative environment. | 4/10/2023 |
| 4933 | EMD Serono Rockville, MD Associate Scientist 2 - 2nd Shift Bachelor’s Degree in a scientific discipline (e.g., Biology, Chemistry, Microbiology, etc. ). Exp: 1+ years |
At MilliporeSigma, as an Associate Scientist 2 – 2nd Shift , you will perform assays and safety testing required to manufacture clinical and commercial products. You will make scientific observations, maintain detailed workbooks/documentation, and ensure all documentation fulfills generally accepted professional/industry standards. | 4/10/2023 |
| 4934 | EMD Serono Carlsbad, CA Mechanical Engineer Bachelor’s Degree in Mechanical Engineering, Chemical Engineering, or any engineering discipline. Exp: 1+ years |
The Mechanical Engineer develops new processes for ultra-high purity (UHP) applications in the technologically advanced semiconductor industry (SEMI). You will be part of a small team of engineers and technicians working to develop new products that will package ultra-high purity chemicals meeting rigorous quality and performance requirements. The position will be focused on developing new processes to improve the quality of the products and performing root cause analysis of problems. While the broader company is strongly focused on chemistry, this role is focused on the relevant mechanical aspects. | 4/10/2023 |
| 4935 | EMD Serono Carlsbad, CA Quality Analyst I - Microbiology Bachelor’s Degree in science, Chemistry, Biology, or a similar life science discipline Exp: 1+ years |
As a Quality Analyst I in the Quality Control Environmental Monitoring group, you will support the site by testing the quality of the cleanroom manufacturing environment and ensuring that SAFC Carlsbad adheres to strict regulatory and ISO requirements. Monitoring activities include but are not limited to, collecting surface, air, water, and personnel samples, monitoring manufacturing processes, enumerating microbial plates, data entry, trend analysis, reporting deviations and nonconformances, and investigation support. The role will entail operating in a fast-paced, highly dynamic environment in collaboration with other departments as well as external stakeholders. This role will support the daily operations of the Environmental Monitoring Group, collect samples, process samples, complete documentation, enter data, and review data for Environmental monitoring. | 4/10/2023 |
| 4936 | EMD Serono Carlsbad, CA Specialist II, Analytical Development Master’s Science Degree in chemistry, biochemistry, biology, or other life science studies. Exp: 6 months |
MilliporeSigma is seeking a motivated Specialist II to join its dynamic and collaborative Process and Analytical Development team at the Carlsbad viral vector CDMO facility. The successful candidate will contribute to the development and execution of analytical assays for innovative viral vector therapeutics. | 4/10/2023 |
| 4937 | EMD Serono Sheboygan Falls, WI Quality Assurance Associate Bachelor's Degree in Chemistry, Biology, Healthcare, or other Life Science discipline. Exp: 1+ years |
The Quality Assurance Associate at MilliporeSigma in Sheboygan Falls, WI, will support quality systems, and ensure their alignment with business goals, premier customer expectations and requirements, as well as global business unit best practices. The Associate will establish strong collaborative relationships with all departments within the organization and will deliver on quality and regulatory commitments, working autonomously to effectively manage delivery of results within targeted deadlines. | 4/10/2023 |
| 4938 | EMD Serono Sheboygan Falls, WI Associate Quality Control Chemist (Laboratory) B.S. or B.A. Degree in chemistry, biochemistry,?chemical engineering or other life science discipline. Exp: 1+ years |
Evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. Hours: 4:30 PM - 2:30 AM, Wed – Sa | 4/10/2023 |
| 4939 | Millipore Rockville, MD Associate Scientist 1 Bachelor’s Degree in a scientific field (i.e., Biology, Chemistry, etc.) Exp: 1+ years |
At MilliporeSigma, as an Associate Scientist 1, your activities will support assay development through commercial application of new and innovative service offerings within the biosafety testing space. You are responsible for the scientific integrity of technical work performed in the laboratory, and will make scientific observations, maintain detailed workbooks/documentation, and ensure all documentation fulfills generally accepted professional/industry standards. Hours Monday-Friday 12:00pm-8:00pm | 4/11/2023 |
| 4940 | Millipore Kankakee, IL Quality Control Scientist Bachelor’s degree in Biology, Chemistry, or another related life science discipline. Exp: 1+ years |
At MilliporeSigma, the Quality Control Scientist is responsible for performing multi-discipline analytical test methods for a variety of product lines to help achieve overall business objectives. This role is also responsible for maintaining the Product Stability, Product Retention, and Reverse Osmosis Water Quality Programs in accordance with the current regulatory guidelines. Additionally, this role supports Special Projects and Process Engineering analytical requirements to maintain existing, and future, business development. | 4/11/2023 |
| 4941 | Millipore Carlsbad, CA Quality Analyst II, Microbiology Bachelor’s Degree in science, Chemistry, Biology or similar life science discipline. Exp: 1+ years |
As a Quality Analyst II in the Quality Control Microbiology group, you will support the site by performing environmental monitoring of the cleanroom manufacturing environment as well as microbiological testing of pharmaceutical grade water systems, raw materials, and production samples. Environmental Monitoring responsibilities include, but are not limited to, collecting surface, air, water, and personnel samples, monitoring manufacturing processes, enumerating microbial plates, data entry, trend analysis, reporting deviations and nonconformances, and investigation support. Laboratory Testing responsibilities include, but are not limited to, bioburden testing, endotoxin testing, media fill testing, growth promotion testing, and biological indicator testing. The Carlsbad Viral Vector Manufacturing Facilities are a CDTMO focused on viral vectors and gene therapies. The role will entail operating in a fast-paced, highly dynamic environment in collaboration with other departments as well as external stakeholders. A role in Quality Control offers the opportunity to work with and learn about all the different aspects of the organization, from Facilities to Validation to Manufacturing and Quality Assurance. | 4/11/2023 |
| 4942 | Millipore Jaffrey, NH QC Supervisor, Physical Test Lab Master’s Degree or higher-level education in Chemistry, Chemical Engineering, Biochemistry, or Biology Exp: 1+ years |
As a Quality Supervisor at MilliporeSigma in Jaffrey NH, you will be supervising and supporting a laboratory group of personnel and resources for QC Labs. A Shift: Monday - Friday 8 AM - 5 PM | 4/11/2023 |
| 4943 | Millipore St. Louis, MO GMP Engineering And Maintenance Compliance Associate Bachelor’s degree in Engineering Exp: 1+ years |
MilliporeSigma has an exciting opening at their Cherokee/St. Louis site. The Engineering and Maintenance Compliance Specialist's primary role is to provide support to the cGMP operations. This position will be responsible for assisting Engineering, Manufacturing, Technical Operations, and QA with quality support as it relates to change control, equipment non-conformances, process deviations, routine equipment system maintenance and Building Management System support. Additional responsibilities may include on the floor oversight during manufacturing, incident investigations and resolution, monitoring of the building management system. | 4/11/2023 |
| 4944 | Millipore St. Louis, MO Research And Development Scientist Master’s degree in a scientific discipline Exp: 1+ year |
Your Role: Design and implement experimental plans and procedures. Responsible for the scientific integrity of technical work performed in the laboratory and maintain detailed workbooks and documentation. The purpose of this position is to support R&D efforts for designing new products and/or platform technologies. Incumbent will assist in development and commercialization of new product offerings by developing and executing a broad range of protocols. This position is located at the Laclede Avenue location. | 4/11/2023 |
| 4945 | Endo Pharmaceuticals Rochester, MI Quality Associate Specialist, Product Release - Afternoon Shift BA/BS degree in a related discipline. Exp: 0-1 year |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. | 4/11/2023 |
| 4946 | Endo Pharmaceuticals Rochester, MI Quality Associate Specialist, Product Release - Midnight Shift BA/BS degree in a related discipline. Exp: 0-1 year |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. | 4/11/2023 |
| 4947 | Entrada Therapeutics Boston, MA Research Associate, Process Chemistry CONTRACT Bachelors and/or masters in biochemistry, chemistry, chemical, or biological engineering, or a related discipline. Exp: 0‑2 years |
The Opportunity Routinely support operation of large-scale solid-phase reactors Learn the workflows of technical teams by shadowing lab scientists Identify and/or optimize operations to improve process robustness, throughput, and cost while maintaining product quality Assist with data management and assay analysis Works towards future scalability Provide mentorship to peers work toward an efficiently cross trained team | 4/12/2023 |
| 4948 | Federation Bio South San Francisco, CA Research Associate I Bachelor of Science degree in a Life Sciences discipline. Exp: (1) year |
We are seeking an individual to play a key role in our team in supporting critical research and IND-enabling animal studies. A successful candidate is required to have prior animal husbandry experience and proficiency in rodent biomethods. This role will be responsible for day-to-day maintenance of the animal vivarium where germ-free, gnotobiotic, and specific-pathogen free mice are maintained. The ideal candidate will need to demonstrate aptitudes in foresight, planning and ability to organize and schedule the many tasks associated with running an animal facility. The candidate should be flexible, excited to wear the many hats to meet the dynamic needs of a start-up environment, proactive and positive. This person should also have the desire to contribute to a vibrant and dynamic culture. Some ability to build and assemble equipment is desired. Understanding the principles of sterilization is an integral component of this position. Must have the ability to lift 50 pounds and stand for extended periods of time. Some work on weekends may be required. This position will report to Federation Bio’s head of in vivo sciences. This is an in-person position and located in South San Francisco, CA. | 4/13/2023 |
| 4949 | Forge Biologics Columbus, OH Associate Scientist/Senior Associate Scientist, Process Development - Upstream Master’s degree in Biology, Chemistry, or relevant area. Exp: 0+ years |
We are currently seeking an Associate Scientist/Senior Associate Scientist, Process Development - Upstream to join the Forge Biologics team. This is an exciting opportunity to assist in the execution of laboratory experiments and protocols for upstream process development efforts. The candidate will assist in process development protocols/studies to optimize procedures for unique viral vector platform process and to assist in the transfer of client programs. The Associate Scientist/Senior Associate Scientist will work to meet production goals, notify management of any potential delays in the schedule, and make recommendations to resolve the issues. This position reports to the Scientist II, Process Development - Upstream and is responsible for laboratory stocking, inventory management, and assisting in laboratory activities. This includes preparing growth media, chemical buffers, solutions or other reagents that involve the mixing of subcomponents and preparing raw materials for use in production steps. Work activities may also include performing laboratory techniques (cell culture, vector purification) in support of production of viral vectors. It is expected that this individual will work as a member of the development team while accomplishing the timely completion of assignments and reporting of unexpected technical issues. | 4/13/2023 |
| 4950 | FORMA Therapeutics West Lebanon, NH Cell Therapy Associate Master’s Degree in Cell Biology, Molecular Biology or a closely related field. Exp: one (1) year |
This position has the responsibility of working with senior level Scientists and manufacturing associates to execute process development, scale-up, tech transfers, and validation studies in support of manufacturing or analytics. Additionally, the role will necessitate experimental troubleshooting, GMP documentation and laboratory investigations. The position will require understanding the underlying science of the process and manufacturing equipment, or assay methods and instruments. | 4/13/2023 |
| 4951 | FORMA Therapeutics Clayton, NC Quality Control Analyst I or II BA/BS in a science or related field of study Exp: one (1) year |
Perform & review analysis of in-process, release & stability samples of API &/or filled product in accordance with cGMP, site & corporate procedures & policies. Transfer of technology & processes in accordance with relevant project plans & timelines. This is a Quality Control chemistry laboratory group focusing on incoming raw materials. | 4/13/2023 |
| 4952 | FORMA Therapeutics Clayton, NC Quality Control Analyst I or II BA/BS in a science or related field of study Exp: one (1) year |
Perform & review analysis of in-process, release & stability samples of API &/or filled product in accordance with cGMP, site & corporate procedures & policies. Transfer of technology & processes in accordance with relevant project plans & timelines. | 4/13/2023 |
| 4953 | FORMA Therapeutics West Lebanon, NH Quality Control Microbiologist (Sr. Level Experience Preferred) Bachelor’s degree in a scientific discipline or equivalent. Exp: zero (0) to two (2) years |
This position carries out routine microbiological testing to support the manufacturing facility. All work is carried out in a QC GMP environment where the highest level of compliance and attention to detail is necessary. Role focuses on routine activities such as utility and facility monitoring, data reporting, general laboratory support and activity coordination. This individual works with supervision/instruction on routine work and detailed instruction for new activities. This position schedule is Tuesday-Saturday from 8:00am-5:00pm. | 4/13/2023 |
| 4954 | FORMA Therapeutics West Lebanon, NH Manufacturing Science and Analytical Technology Associate I Bachelor’s degree or equivalent in Biochemistry, Chemistry, Engineering or a closely related field. Exp: one year |
This position has the responsibility of working with senior level Scientists to execute laboratory scale process development or validation studies in support of process or assay development, or process troubleshooting or scale-up. The scientific knowledge in this position will range from familiarity with details of manufacturing process, process chemistries, development studies and relevant assay methods and instruments. This position will be one of the interfaces between MSAT and Manufacturing or Quality. | 4/13/2023 |
| 4955 | FORMA Therapeutics West Lebanon, NH Manufacturing Technician (Levels I-IV) Bachelors’ Degree in a science discipline. Exp: zero (0) years’ |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. Our Manufacturing Technicians work 12-hour shifts and we offer the following schedules: Day Shift (7am-7pm) Sunday-Tuesday and everyother Wednesday Thursday-Saturday and everyother Wednesday Night Shift (7pm-7am): Sunday-Tuesday and everyother Saturday Wednesday-Friday and everyother Saturday | 4/13/2023 |
| 4956 | Frenova Renal Research Lawrence, MA Mechanical Engineer I Bachelor's Degree in related Engineering or scientific discipline required Exp: 0 - 2 years' |
The entry level Engineer will participate in designing, executing, and championing research and development activities of Fresenius' products. As a member of a tech team, the Engineer I environment is mentored - with oversight from higher level Engineers to complete pre-defined work. The Engineer I may be involved in quality planning, internal audits, data collection and analysis, specification development and review and design review and qualification. The Engineer I will work with cross-functional teams to develop, commercialize, and maintain high quality. | 4/14/2023 |
| 4957 | Frenova Renal Research Ogden, UT R & D Engineer I - Dialyzers Bachelor's Degree in related Engineering or scientific discipline required Exp: 0 - 2 years' |
The entry level Engineer will participate in designing, executing, and championing research and development activities of Fresenius' products. As a member of a tech team, the Engineer I environment is mentored - with oversight from higher level Engineers to complete pre-defined work. The Engineer I may be involved in quality planning, internal audits, data collection and analysis, specification development and review and design review and qualification. The Engineer I will work with cross-functional teams to develop, commercialize, and maintain high quality. | 4/14/2023 |
| 4958 | Frenova Renal Research Southhaven, MS Medical Lab Scientist - Trace Bachelor’s Degree in Medical Laboratory Sciences or Biological Sciences required. Exp: 0 – 3 years’ |
Now offering a $2,000 sign on bonus PURPOSE AND SCOPE: Performs a wide variety of moderately and highly complex tasks and analysis of human fluids and tissues, using manual procedures as well as operating various laboratory equipment and automated analyzer systems. Responsible for acceptable quality control accurate testing, and release of accurate patient results in collaboration with the Lead, Supervisor or Manager. | 4/14/2023 |
| 4959 | Catalent Greenville, NC Analytical Chemist I Bachelor’s degree a science-related discipline (e.g. Biology, Chemistry, Pharmaceutical Sciences). Exp: 0+ years |
Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. The Analytical Chemist I primarily performs routine analytical testing in support of pharmaceutical products following all applicable safety, quality, and regulation requirements. | 4/5/2023 |
| 4960 | Catalent Morrisville, NC Associate Scientist Master’s degree Exp: 0 years |
Catalent Pharma Solutions is Morrisville, NC is hiring an Associate Scientist for the Laboratory Group. The laboratory groups at Catalent RTP are responsible for the support of pharmaceutical product development in a range of dosage forms both directly with customers and in collaboration with other Catalent facilities. This includes formulation development, structural chemistry, analytical support, and clinical trials material manufacturing. | 4/5/2023 |
| 4961 | Catalent St. Petersburg, FL Associate Scientist II, Quality Control Requires BS or BA with college course work in related sciences, analytical laboratory experience preferred but not required. Exp: 0 years |
The Associate Scientist II, Quality Control will Independently test, develop and implement assays useful for the identification and characterization of Raw Materials, pre-capsulation, Stability and Finished Products. Analyze data, document results, maintain laboratory notebook according to cGMP and Internal guidelines. Communicate results in written and oral presentations. Help in writing Procedures, Specifications and Test Methods. Keep abreast of literature in field; help train colleagues; contribute to continuous improvement within the group. Comply with FDA, EPA and OSHA regulations, performing all work in a safe manner. Maintain proper records in accordance with all SOP's and policies. | 4/5/2023 |
| 4962 | Catalent St. Petersburg, FL Associate Scientist II Requires BS with college course work in related sciences. Analytical laboratory experience preferred not required. Exp: 0 years |
The Associate Scientist II, Quality Control will Independently test, develop and implement assays useful for the identification and characterization of Raw Materials, pre-capsulation, Stability and Finished Products. Analyze data, document results, maintain laboratory notebook according to cGMP and Internal guidelines. Communicate results in written and oral presentations. Help in writing Procedures, Specifications and Test Methods. Keep abreast of literature in field; help train colleagues; contribute to continuous improvement within the group. Comply with FDA, EPA and OSHA regulations, performing all work in a safe manner. Maintain proper records in accordance with all SOP's and policies. | 4/5/2023 |
| 4963 | Catalent Kansas City, MO Quality Control Associate Scientist II Bachelor's degree in related life science or physical science field. Exp: 0+ years |
Catalent Pharma Solutions in Kansas City, MO is hiring a Quality Control Associate Scientist II. The Quality Control Associate Scientist II under close supervision and guidance, performs tasks from detailed instructions and established procedures. Comply with site SXPs, corporate policies, and Environmental Health and Safety requirements. Has basic knowledge of the principles and concepts of discipline (e.g. Biology, Chemistry). Applies technical skills to complete assigned work within own group/project team. A self-motivated, detail-oriented person who is able to make decisions and solve problems is essential. Able to work independently with little to no supervision, and flexible to also assist team members as needed. | 4/5/2023 |
| 4964 | Catalent Kansas City, MO Pharmaceutical Development Associate Scientist II Bachelor's degree in related life science or physical science field is required. Exp: 0+ years |
Catalent Pharma Solutions in Kansas City, MO is hiring a Pharmaceutical Development Associate Scientist II. The Kansas City Pharmaceutical Development Associate Scientist II supports formulation/process design and development of oral solid dosage forms. Participates/leads in clinical trial manufacturing endeavors and ensures that all work is carried out in compliance with regulatory requirements, good manufacturing practices (cGMP) and standard operating procedures (SOPs) | 4/5/2023 |
| 4965 | Catalog Charlestown, MA Associate Process Engineer- DNA Synthesis A BS in mechanical or biochemical engineering. Exp: 1-2 years |
CATALOG is a rapidly expanding, Boston-based start-up on a mission to enable new paradigms for data preservation and computation. We are looking for a motivated entry-level engineer eager to work with an interdisciplinary team of biologists, engineers, and computer scientists. You will be responsible for routine operation and maintenance of our proprietary high throughput DNA writing system, used to build vast sets of information-encoding synthetic DNA molecules. As part of our rapidly expanding group, you will help to build, optimize, and evaluate molecular datasets at a scale enabling novel applications for the world’s first DNA storage and computing platform. | 4/5/2023 |
| 4966 | Catalog Charlestown, MA Research Associate, Molecular Biology MS in biochemistry, molecular/synthetic biology or a related field. Exp: 0 years |
CATALOG is a well-funded, rapidly expanding, Boston-based start -up on a mission to preserve and compute on the world’s most valuable data. We are growing our team to build CATALOG’s DNA-based data storage and computation platform. We are looking for a motivated Scientist with a background in synthetic biology to join our interdisciplinary team of biologists, engineers, and computer scientists to design novel storage and computing architectures and translate them into scalable read/write operations. As part of the newly established Future Technologies group, you will help to build and evaluate novel synthetic biology strategies that help realize the world’s first DNA storage and computing platform. | 4/5/2023 |
| 4967 | Cayman Chemical Ann Arbor, MI Associate Scientist - NMR Specialist Master’s degree in chemistry or related field. Exp: none (with Master’s degree) |
Responsibilities and Duties: Apply knowledge of NMR spectroscopy to support structure elucidation of Cayman’s research chemicals Operate and maintain NMR and MS instrumentation Process and interpret NMR spectra for entry into a spectral database Collaborate with quality control to perform and evaluate NMR testing on catalog products Perform routine NMR maintenance including cryogen fills, shim optimization, and pulse width calibration Work with supervisor and manager to align priorities to Analytical Chemistry Division goals Substantively contribute to regular group, project team, and departmental meetings Assist with general upkeep of the NMR lab | 4/5/2023 |
| 4968 | Cisbio San Diego, CA Research Associate - Antibody Development Bachelor of Science with a discipline in cell biology, immunology, and biochemistry preferred. Exp: 1-2 yrs |
This person would be responsible for developing phosphosite specific monoclonal antibodies in BioLegend derived from immunized animals by performing antigen preparation, host immunization, bleed analysis, and cell lysate preparation. Techniques involved in this job include antigen formulation, animal immunization and tissue harvesting, cell culture and antibody analysis using ELISA and Western blot techniques. | 4/5/2023 |
| 4969 | Cisbio San Diego, CA Research Associate - Exploratory R&D B. S. or M.S. in Biology, Immunology or another related field. Exp: 1 year |
The Research Assistant will be involved in product development and optimization of cell culture process and new product development. In particular, he/she will be involved in determining the feasibility of new products and new cell culture processes for in-house and custom projects. This role will also be involved in troubleshooting issues associated with cell culture. This role requires mammalian cell culture experience. Knowledge of process development for antibody production, particularly hybridoma, on a small and large scale is a plus. He/she must have excellent organizational skills, attention to detail, and accuracy. Be able to maintain good documentation practices and generate reports. Must be proficient in computer software use (Excel, Word, and PowerPoint). Must be self-motivated and able to multi-task. Must be collaborative and have good communication skills. | 4/5/2023 |
| 4970 | Cisbio San Diego, CA Research Associate - Recombinant Protein & Molecular Cloning BS in biological sciences. Exp: 1 year |
This position is responsible for developing cutting edge recombinant protein research products in Molecular Cellular Biology group. The research associate will be involved on developing a new line of recombinant protein products by supporting other team members. The duties include preparing buffer solutions and cell culture media, performing PCR and DNA purification according to standard operating procedures, performing bacterial and mammalian cells cultures, and purifying recombinant proteins with affinity tag. This position offers a significant opportunity for learning molecular biology techniques and career growth in the biotechnology industry. | 4/5/2023 |
| 4971 | Cisbio Pittsburgh, PA Molecular Laboratory Technologist Bachelor's degree in biology or related scientific discipline. Exp: 0-2+ years |
Performs clinical genetic laboratory tests, procedures and analysis to provide data for diagnosis, treatment, and prevention of disease in adults, children, and newborns. | 4/5/2023 |
| 4972 | Cognate Biosciences Rockville, MD Biomanufacturing Associate I Bachelors degree in biology/life sciences, bioengineering, or related discipline. Exp: 0-1 year |
The Biomanufacturing Associate I will play an integral role within CRL’s gene therapy manufacturing function by understanding and applying biological, bioprocess, manufacturing, and mechanical principles, processes, procedures, inputs, and outputs, for designated production processes and handovers, within a cGMP and GLP environment. This will ensure the timely production and release of quality products, based on client specifications. This role will perform a range of routine and semi-routine tasks, some of which are moderately difficult, requiring judgment in resolving issues or making recommendations, with guidance as needed, in order to proficiently execute manufacturing protocols in a regulated environment. | 4/5/2023 |
| 4973 | Cognate Biosciences Cleveland, OH Research Analyst I Bioanalytical Chemistry Bachelor’s degree (BA/BS) or equivalent experience. Exp: 0 year |
We are seeking a Reseach Analyst 1- Bioanalytical Chemistry for our Safety Assessment CRL Site located in Cleveland, OH. | 4/5/2023 |
| 4974 | Cognate Biosciences Spencerville, OH Research Technician I BA/BS in a life science field preferred. Exp: 0-6 months |
We are seeking an experienced Research Technician Assistant for our Toxicology Team located in Spencerville, OH. Do you have experience working with animals? 4H? FFA? Vet Assistant? Farm/AG? Or a medical background working in hospitals/STNA/EMT? This could be a great fit for you. A Research Technician Assistant is responsible for: collecting and recording data in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Hourly Rates $18-$19/hr. $1000 Sign on Bonus. 3 weeks vacation and additional sick time. | 4/5/2023 |
| 4975 | Cognate Biosciences Shrewsbury, MA Research Technician I Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months to 1 year |
Charles River Laboratories is seeking an Research Technician I for our InVivo (InLife) Team within our Safety Assessment site located in Shrewsbury, MA. The Research Technician 1 will collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods. | 4/5/2023 |
| 4976 | Cognate Biosciences Rockville, MD Bioprocess Engineer I B.S. in Chemical Engineering, Bioengineering, Chemistry, Biochemistry, or related subject area. Exp: 1 – 4 years |
The Bioprocess Engineer I is responsible for the accurate and timely scale up of process development data to large scale manufacturing. This responsibility includes scale up, document authorship, process data tracking, deviation investigation, and data analysis to ensure right-first-time clinical and commercial manufacturing and continuous improvement. This position interacts with Process Development, Manufacturing, Facilities, Quality Control, Quality Assurance, and Supply Chain to ensure project success. | 4/5/2023 |
| 4977 | Cognate Biosciences Newark, DE Research Associate Bachelor's degree (B.A./B.S.) or equivalent in Microbiology or Molecular biology or related scientific field. Exp: 1 to 2 years |
The Microbial Solutions team located in Newark, DE is seeking a Research Associate. This role will be responsible for assisting with experimental design, performing experiments and analyzing data to support new product and service development and associated support functions related to Research and Development within Microbial Solutions. | 4/5/2023 |
| 4978 | CooperSurgical Tucson, AZ Technician I - Quality Control Bachelor’s degree in one of the biological, chemical, or physical sciences. Exp: 0 - 1 year |
Cord Blood Registry (Cbr) Technician I - Quality Control is responsible for analyzing and documenting test results from our cord blood and cord tissue processed samples, releasing raw materials, supporting the analytical and processing equipment maintenance program, conducting environmental monitoring, and providing a wide range of critical functions that support the cryogenic storage of our client’s final product. This position is also responsible for providing our internal customers with technical expertise while maintaining the highest quality services possible | 4/6/2023 |
| 4979 | CordenPharma Boulder, CO QC Analyst - Nights Bachelor's Degree (BA) from 4-year college or university. Exp: 0-1 year |
Performs all technician tasks accurately and efficiently without supervision. Initiates expert technical advice to customers and completes all tasks in the Technician Training Manual. Maintains a high level of housekeeping and attention to detail. | 4/7/2023 |
| 4980 | CordenPharma Boulder, CO Night - Standards and Stability Analytical Chemist Bachelor's degree (BA) from a 4-year college or university. Exp: 0-1 year |
This is the intermediate level technical professional within the R&D Team. Performs analytical tasks accurately and efficiently without supervision, to qualify standards, support the Stability Program, and support on-going development projects. | 4/7/2023 |
| 4981 | Contract Pharmacal Hauppauge, NY Chemist (Quality Control) Bachelor’s degree in Chemistry or related science required. Exp: 1-9 years |
The Chemist, QC position is responsible for and has experience in performing chemical testing and completion of real-time documentation per cGMPs and current SOPs. | 4/7/2023 |
| 4982 | Culture Biosciences South San Francisco, CA Bioprocess Associate, Cell Culture Bachelor’s degree in Biology, Microbiology, Chemical Engineering, Biotechnology or a science related background. Exp: 1-2 years |
We are looking for a Bioprocess Associate, with experience in bioreactors and mammalian cell culture, to join our bioreactor operations team. Your work will contribute to getting novel biotechnology products to market faster and more efficiently. Your job will be to work as part of a team of bioprocess associates, engineers and project leads to execute customer projects and build an efficient operations department. In particular, you will learn mammalian cell culture techniques and work with in-house custom built software and equipment designed for bioreactor operations. | 4/7/2023 |
| 4983 | Cytovance Biologics Oklahoma City, OK QC Stability Associate QC Stability Associate B.S. in Life Sciences/Chemistry Exp: 1-3 years |
The Stability Associate will participate in the QC Stability Study Program activities which includes designing and drafting stability study protocols according to ICH guidance for drug substance, drug product and reference standard, participate in range of quality control analytical activities such as analytical assay performance, and transfer of standard protein characterization methods. Duties will be carried out in accordance with quality standards and procedures set by the company and applicable government agencies | 4/7/2023 |
| 4984 | Cytrellis Biosystems Woburn, MA Mechanical Engineer Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or equivalent job experience. Exp: 0 – 3 years |
The Mechanical Engineer is responsible for the mechanical design and development of our future product platforms in a highly collaborative environment. The Mechanical Engineer develops a thorough understanding of the product technology, leads the mechanical development of next generation devices, and demonstrates technical feasibility through analysis and testing. The position may be required to perform all, or a combination of the following essential responsibilities as determined by necessity. This role is located at the Company’s Woburn, MA office. | 4/7/2023 |
| 4985 | Day Zero Diagnostics Boston, MA Lab Research Associate II / Senior Research Associate Bachelor's Degree in molecular biology, biochemistry or microbiology from a four-year college/university. Exp: 1-2 years |
The Lab Research Associate II/ Senior RA will work closely with an interdisciplinary team of scientists, RAs, and engineers to test and optimize our diagnostic workflows to support DZD’s efforts to develop a commercial diagnostic device. | 4/7/2023 |
| 4986 | Dendreon Seal Beach, CA TEMP-HIRE Manufacturing Operations Associate BA/BS degree in Science. Exp: 0 years |
Aseptic manufacturing and assembly of clinical and commercial human blood derived components in a clean-room environment (Class 10,000/ISO7, and Class 100,000/ISO8). | 4/7/2023 |
| 4987 | DiaCarta Pleasanton, CA Clinical Laboratory Assistant BS/BA in life science is a plus. Exp: 0-1 year |
A CLA performs laboratory duties under the supervision of a licensed CLS. This position is for assisting the CLS and for sample processing, equipment operation and maintenance, and documents. | 4/7/2023 |
| 4988 | DiaCarta Pleasanton, CA Research Associate S. degree in molecular biology or a related field Exp: 0-2 years |
DiaCarta is seeking a highly motivated, independent, and interactive Research Associate to join the R&D function in the company. The new team member will participate in R&D activities with the goal of developing and launching new qPCR, NGS, and branched DNA tests for IVD cancer diagnostics applications. The successful candidate will have outstanding attention to detail, enjoy working in a fast-paced multidisciplinary team environment, and have exceptional hands-on laboratory skills. DiaCarta is a rapidly growing company, so the candidate must be highly motivated and committed to launching their career in an innovative area of molecular diagnostics. This is a full-time role in Richmond, and you will be reporting to the Senior Scientist. | 4/7/2023 |
| 4989 | DiaCarta Pleasanton, CA Manufacture Technician S. degree in Molecular Biology, Cell Biology, Biotechnology or related field Exp: 1-year |
This position is a member of a fast-paced production team and will be responsible for the following tasks. Purchase raw materials from a vendor Receive incoming materials and perform inspection and inventory recording Production of DiaCarta IVD products to meet sales demands Labeling of raw materials and finished goods Perform calibration or preventative maintenance of the instrument Participate in process improvement projects Compliance with corporate quality systems Other on-the-job assignments indicated by management | 4/7/2023 |
| 4990 | Dice Therapeutics South San Francisco, CA Research Associate / Senior Research Associate in Medicinal Chemistry BS or MS in organic chemistry. Exp: 0-6 years |
We seek an exceptional full-time lab-based synthetic chemistry Research Associate / Senior Research Associate to join our medicinal chemistry team. This individual will be a key contributor to the synthesis of intermediates and final compounds within the goals of developing treatments for inflammatory diseases. Must have legal right to work in US. | 4/7/2023 |
| 4991 | DiscGenics Salt Lake City , UT QA/QC Analyst I Bachelor’s degree in the Biological Sciences, or related field. Exp: 1 year |
This is a hybrid role with responsibilities for QA and QC, depending on the needs of DiscGenics as we grow. The Analyst I, QA/QC is responsible for supporting functional leaders and managers to establish and grow Quality related documentation and processes reporting directly to the Manager, Quality Assurance. The Analyst I, QA/QC Provides guidance on quality assurance initiatives to ensure that operations remain in a state of compliance with applicable regulations for biologics including cell therapies. This role interacts with all levels of the organization. Delivers collaborative and positive leadership to facilitate department and organizational initiatives for cultural cohesion aligned to the DiscGenics Values. | 4/7/2023 |
| 4992 | Distributed Bio Mattawan, MI Research Analyst I- Formulations Bachelor’s/Master’s degree in a relevant field. Exp: 0 year |
We are seeking a Research Analyst I for our Test Material Control/Formulations Department site located Mattawan, MI. A Research Analyst I - Test Material Control (TMC)/Formulations is responsible for: preparing, sampling, and dispensing formulated test material according to applicable Standard Operating Procedures (SOPs) and GxP guidelines. The individual in this role: completes projects on time while maintaining quality and efficiency; communicates effectively with management, internal customers, and team members; assists others with their duties; and may assist with troubleshooting formulation issues. The pay range for this position is $23/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. The shift is for the weekend, Friday to Monday 6 AM-2:30 PM but will train for the first 12 weeks Monday-Friday 6 AM-2:30 PM. When you work Saturday or Sunday there will be a 10% shift differential. | 4/7/2023 |
| 4993 | Distributed Bio South San Francisco, CA Research Study Technician I Bachelor's (B.A./B.S.) Degree preferred. Exp: 6-12 months |
We are looking for a Research Study Technician to join our Insourcing Solutions team, located in South San Francisco, Ca. | 4/7/2023 |
| 4994 | Distributed Bio Mattawan, MI Research Analyst I - Pharmacy Bachelor's/Master's degree in a relevant field. Exp: 0 years |
We are seeking an experienced Research Analyst 1 for our Pharmacy Team in Mattawan MI. | 4/7/2023 |
| 4995 | Distributed Bio Newark, DE Research Associate I Bachelor’s degree (B.A./B.S.) or equivalent in a scientific discipline. Exp: 0-2 years |
We are seeking an experienced Research Associate for our Microbial Databases and Technology Transfer group located in Newark, DE. . This role will be Responsible for performing routine experiments and analyzing data to support new product and service development and associated support functions related to daily operations of Microbial Databases and Technology Transfer group. | 4/7/2023 |
| 4996 | Distributed Bio Reno, NV Research Analyst I - Bio/Immunology 1 Bachelor’s degree (B.A. / B.S.) in biological science or related discipline required. Exp: 6 Months |
We are seeking a Research Analyst Ifor our Safety Assessment site located in Reno, NV. This position will be responsible for handling and processing samples, and performing accurate data collection and reporting. Basic methods will be used to perform laboratory tasks with minimal supervision in the performance of studies. | 4/7/2023 |
| 4997 | Distributed Bio Bethesda, MD Bacteriology Technician - Floater ($1K Sign-on Bonus) Bachelor’s degree in Biological Sciences or related discipline is required. Exp: 0-2 years |
In the Bacteriology Technician Floater role, you will use existing SOPs and quality assurance standards to perform routine gross necropsy and parasitology exams of lab animals, as well as prepare and examine collected tissue for further evolution, and prepare blood samples for shipment. You will also be asked to gather and prepare lab materials; assist with receipt, stocking, and ordering of supplies; and assist with other duties in the main lab. In this role, you will also access, set up, and run incoming samples; as well as update appropriate databases and written logs for every sample; access and plate environmental submissions; and plate incubated broths onto appropriate media. The Bacteriology Technician Floater will also work interactively with various staff and customers to resolve concerns and offer technical assistance, including preparing and submitting written reports, charts, logs, and inventories. You will need to ensure accurate records of data, and you may be tasked with creating worksheets or spreadsheets to help the lab run more efficiently. You should expect to update records for instrument maintenance and performance, and you may be asked to make mechanical repairs, when possible. Other duties may include operating required equipment and general housekeeping, when required. | 4/7/2023 |
| 4998 | Diversigen Minneapolis, MN Laboratory Technician B.Sc. or M.S. degree in Biology, Biochemistry, Molecular Biology Exp: 0 - 1+ year |
As a Lab Technician I you will be expected to work collaboratively as part of a team. In this role, the Lab Technician I will be responsible for managing timelines, performing hands-on lab work, maintaining processing records and working in compliance with our accreditations and quality standards. | 4/7/2023 |
| 4999 | Bardy Diagnostics Round Lake, IL Research Associate II Master’s degree in chemistry such as analytical or organic chemistry. Exp: 0-2 years |
We currently have an opening for a Research Associate II who can effectively contribute to laboratory operations, laboratory analysts, and facilitate operational excellence in the Medication Delivery R&D Extractables and Leachables laboratories in Round Lake, Illinois. | 3/20/2023 |
| 5000 | Bardy Diagnostics Skaneateles Falls, NY Test Engineer Bachelor’s degree (Mechanical, Electrical, Software, Biomedical Engineering, or comparable technical discipline). Exp: 1 year |
As a member of the Baxter research & development team, you will assist in the world class development of new medical products.This role is responsible for Test Engineering as a member of the new product development team. In this position you will understand and define verification and reliability test protocols, contribute to customer needs, technical risks, product functionality and performance requirements. You will collaborate with other team members to determine what verification is required, including the amount of data required and the methodology for collecting and analyzing the data. Lastly, you will provide objective evidence that a product design meets its specified requirements and meets the identified user’s needs and intended uses. | 3/21/2023 |
| 5001 | Bardy Diagnostics Bellevue, WA Electrical Engineer (Hybrid) Bachelor's degree in electrical engineering or other technical or science field. Exp: 0 -1+ years |
Your talent is needed across a wide variety of industries. As an Electrical Engineer, you have a wide array of career choices, but are motivated by the opportunity to work in a company that supports innovation, professional development, and a purposeful mission. | 3/21/2023 |
| 5002 | Bardy Diagnostics Skaneateles Falls, NY Mechanical Engineer (Hybrid) Masters Degree in Mechanical Engineering, Mechanical Engineering Technology or equivalent. Exp: 1+ years |
A successful candidate in this role will engage in mechanical engineering activities as part of a broader team to develop new medical products. This role will ensure effective resolution to design related issues, develop new products to grow the business, and ensure compliance with product related standards. | 3/21/2023 |
| 5003 | Bardy Diagnostics Marion, NC Associate I, Quality Lab - Endotoxin B.S. degree in Microbiology, Biology, or related science Exp: 0-2 years |
Conduct microbiological analysis on raw materials, solution, and water samples following approved Standard Operating Procedures in an accurate and timely manner. | 3/21/2023 |
| 5004 | Bardy Diagnostics Cleveland, MS Quality Associate I - Cleaning and Sanitization (3rd shift) Bachelor’s degree in the sciences or in engineering required. Exp: 1 year or more |
Responsible for quality assurance operation in the Solution Focus Factory (Plastic Pour Bottle/Glass/Vials Cleaning and Sanitization). Identify and assess regulatory and quality risks in activities and processes according to regulatory agency rules and guidelines and Baxter quality practices. Provide incoming, in-process and finished goods testing support. Involved in the development and revision of new standard procedures and training of employees. Assist department managers in audits or assessments and closures. Analyze and complete customer complaints. Perform department equipment and process validations. Serve as technical liaison among QM functional groups as well as other departments in the plant. | 3/21/2023 |
| 5005 | BASi Research Products Raleigh, NC Formulation Scientist I B.S. degree in chemistry or related field. Exp: 1 - 3 years |
Responsibilities of the Formulations Scientist include (but are not limited to): prepare formulations for GLP-compliant and non-GLP studies; coordinate with Study Directors, Project Managers, and the formulation manager to ensure timely preparation and delivery of formulations for in-house studies; set up paperwork, perform calculations, and prepare formulations to support toxicology studies; coordinate and maintain ILS chemical repository inventory as needed; archive test chemical samples for studies, as needed; coordinate with Study Directors and outside analytical laboratories as needed for preparation and shipment of formulation samples; assist with company-wide collection and disposal of hazardous waste and equipment calibrations; perform laboratory maintenance tasks (e.g. equipment monitoring/maintenance, disposal of expired chemicals, laboratory clean-up, etc.); maintain supply inventories and prepare purchase orders as needed; maintain accurate study forms/records; handle data (e.g. organize data, prepare data tables); assist in the preparation of protocols, reports, SOPs, presentations as needed; work independently with detailed instruction and minor oversight; work in a team environment with a professional and positive attitude. Other duties as needed. | 3/21/2023 |
| 5006 | BASi Research Products Gaithersburg, MD Sample Management Technician I B.S., B.A., or A.A.S with strong emphasis in life sciences. Exp: 6 months |
Essential Position Responsibilities: Reviews study protocol and ensure study tasks and data for pre-clinical research studies are conducted in accordance with established protocols, SOPs, GLPs, and other pertinent regulatory requirements. Independently generates study forms and worksheets. Prepares sample labels using automated and manual systems and labels cups and tubes for studies. Ensures adequate inventory/supplies are stocked for sample collection. Reviews sample labels and specimens to assure accuracy and quality standards. Prepares blood smears. Operates centrifuge for collected samples in accordance with SOP and protocol requirements and places resulting serum/plasma into appropriate storage tubes Assures proper storage conditions for sample types. Accessions specimens using automated and manual systems. Independently and accurately processes specimens within established metrics. Maintains equipment and instrumentation. Notifies Study Director of sample quality issues and documents appropriately. Manages multiple studies. Learns to perform protocol review in preparation for and attends PI meetings. | 3/21/2023 |
| 5007 | BASi Research Products Boulder, CO Lead Animal Technician B.S./B.A. in science (biology or equivalent). Exp: 1-year |
Assist Study Coordinators to ensure study protocol, schedules, formulations, and sample collections are correct and properly communicated to the research team. Assists Study Coordinators with the creation or verification of cage cards, sample collection prep labels, and data files. Assists in disease induction procedures. Administer doses of compounds to rats and mice via common dosing routes, including but not limited to oral, intravenous, subcutaneous, and intraperitoneal. Perform data collections, including weighing, clinical observations, health assessments, post operative monitoring, and disease progression scoring. Perform blood collections from rats and mice via tail vein, retro-orbital, and terminal blood draws. Processing whole blood collection via centrifugation for plasma and/or serum. Perform behavioral testing (Gait analysis, Von Frey, and Dynamic Weight Bearing testing, etc.) Assist in formulating experimental compounds for administration. Assist in rodent surgeries, including hemostasis, and suturing. Supports and participates in other duties and company initiatives as directed by management. Keep laboratory clean and stocked with supplies. Various software applications sustained by a Windows platform. (Excel, Word, PowerPoint, etc.) | 3/21/2023 |
| 5008 | BASi Research Products West Lafayette, IN Bio Analyst I B.S. in chemistry or biology. Exp: one year |
Conducts sample analysis with data interpretation and basic troubleshooting. Conducts method development and method validation experiments. Assists with general housekeeping and assist other departmental personnel as necessary. | 3/21/2023 |
| 5009 | Bausch & Lomb Greenville, SC Process Engineer I Bachelor’s degree in Chemical, Mechanical, Electrical or Manufacturing Engineering Exp: 1-2 years |
The Process Equipment Engineer will provide value added engineering and leadership to a variety of engineering projects for Lens Care Solutions manufacturing to increase performance, reduce cost, improve quality, and address critical obsolescence issues. Position will also support day-to-day uptime needs of process equipment across the manufacturing site. | 3/22/2023 |
| 5010 | Beckton Dickinson Salt Lake City, UT R&D Engineer I- MDR Remediation B.S. or MS degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering, or other related engineering field. Biomedical Engineering Exp: 1-2 years |
This position will lead the planning, testing, and documentation for EU (European Union) product launches. This position reviews the DHF for released products with regard to compliance to EU MDR, determine gaps, and develops mitigation plans and completes mitigation. The candidate will perform hands-on testing in optimization of a device; conduct process development activities to understand process inputs and outputs; assist/write technical documents, validation protocols and reports; prepare work instructions and standard operating procedures; assist in conducting design and process qualification and validation; support equipment development; support other activities from R&D, Quality, Operations, and Regulatory Affairs. | 3/22/2023 |
| 5011 | Be Biopharma Kendall Square, MA Contract - Sr. Research Associate, Bioassay Development BS or MS in Chemical Engineering, Biology, Analytical Chemistry, Biochemistry, Cell & Molecular Biology, or related discipline. Exp: 1-2 years |
This laboratory-based position is responsible for qualification, and execution of sample analysis using bioanalytical assays, primarily ELISA and MSD based assays, to support Be Bio’s R&D and research pipeline programs. This position will also have the scope of training on other assay types such as FACS and cell culture, to support other cross functional teams within the Be Bio organization. The successful candidate will utilize their knowledge of ELISA to apply these methods to execute assays, perform data analysis and present data to the internal teams. Prior experience in generating and maintaining test methods, assay worksheets, SOPs and R&D processes to GLP standards is desirable. This position has tremendous room for growth and opportunities across multiple areas of the R&D organization. | 3/22/2023 |
| 5012 | BGI San Jose, CA LC/MS Research Associate – Small Molecule B.S. degree with biochemistry/chemistry major or related field. Exp: 0-2 years |
San Jose Mass Spec Lab of BGI Americas is seeking an exceptional and motivated research associate with competitive compensation. The main responsibility of this position includes, but not limited, to support the SJMS production team 1) to turn around routine customer and research projects, 2) to maintenance and operate LC-MS instrument, 3) to assist lab manager to build up metabolomics and lipidomics capability in SJMS lab, 4) to support other departments when needed. A candidate with metabolomics/lipidomics LC-MS experience is a plus; a candidate with small molecule sample prep experience is a plus. An ideal candidate will need to demonstrate that they are capable of consistently following Standard Operational Procedures (SOPs) to consistently perform sample preparation procedures for metabolomic or lipidomics analysis. A candidate with hands-on experience in HPLC, Orbitrap mass spec and working with biofluids is a plus. | 3/22/2023 |
| 5013 | BGI San Jose, CA LC/MS Research Associate – Proteomics B.S. degree with biochemistry/chemistry major or related field. Exp: 0-2 years |
BGI Americas San Jose Mass Spec (SJMS) center is seeking an exceptional and motivated research associate to join our Proteomics department at our San Jose facility. The main responsibility of this position includes, but not limited, to support the SJMS production team 1) to turn around routine customer and research projects, 2) to maintenance and operate LC-MS instrument, 3) to assist lab manager to build up additional proteomics capability in SJMS lab, 4) to support other departments when needed. An ideal candidate will need to demonstrate that they are capable of consistently following Standard Operational Procedures (SOPs) to consistently perform sample preparation procedures for proteomics and biologics characterization analysis. A candidate with hands-on experience in HPLC, Orbitrap mass spec and, working with biofluids is a plus. | 3/22/2023 |
| 5014 | BigHat Biosciences San Mateo, CA Research Associate (Purification) BS or MS in biochemistry/chemistry/biology or related science field. Exp: 1-3 years |
BigHat Biosciences is looking for a motivated and energetic Research Associate with a strong background in protein purification to further advance BigHat’s platform for ML-driven antibody discovery and engineering. | 3/22/2023 |
| 5015 | BioFire Diagnostics Salt Lake City, UT Research Associate I or II B.S. in molecular biology, biology, biomedical sciences, or a related field is desired. Exp: One to two years |
The Molecular Systems Research Associate I or II (RA I/II) position is a full-time, non-exempt position. This position is part of a team working on various laboratory procedures involving nucleic acid isolation methods and PCR under general guidance. This person will work closely with other research associates or scientists in the research lab. | 3/23/2023 |
| 5016 | BioFire Diagnostics Salt Lake City, UT Research Associate I/II Bachelor’s degree in a scientific discipline. Exp: RA I No experienceRA I No experience |
The Research Associate I is a technical hourly position with laboratory responsibilities. The RA I works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of FDA and other regulatory submissions. Tasks will focus on molecular and microbiological experiments and procedures (e.g. nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to communicate and coordinate with peers and supervisor(s) effectively and respectfully. The RA I position requires basic laboratory technical and organizational skills, attention to detail, critical thinking, troubleshooting and problem-solving, and a dedication to the mission and goals of the department and BioFire. A Research Associate I may receive general or detailed instruction and supervision on routine work, and detailed instruction and supervision on new procedures and assignments | 3/23/2023 |
| 5017 | BioFire Diagnostics Salt Lake City, UT Software Engineer I/II/III - Data Engineer B.S. in a quantitative discipline: Computer Science, Software Engineering, Computer Engineering, Information Systems, Statistics, Mathematics, Engine Exp: 0+ years |
bioMérieux is a fast growing and profitable biotech company with a great opportunity for a Software Engineer that is interest in data engineering and software development. This engineer will be joining a team of Software Engineers to support the research and development at bioMérieux. | 3/23/2023 |
| 5018 | BioLegend San Diego, CA Research Associate - Antibody Development Bachelor of Science with a discipline in cell biology, immunology, and biochemistry preferred. Exp: 1-2 yrs |
This person would be responsible for developing phosphosite specific monoclonal antibodies in BioLegend derived from immunized animals by performing antigen preparation, host immunization, bleed analysis, and cell lysate preparation. Techniques involved in this job include antigen formulation, animal immunization and tissue harvesting, cell culture and antibody analysis using ELISA and Western blot techniques. | 3/23/2023 |
| 5019 | BioLegend San Diego, CA Biochemist I - Custom Solutions PURE Bachelor’s degree in Biochemistry, Chemistry, or other related area. Exp: 1 year |
BioLegend has an opening for a self-motivated individual with manufacturing experience in a fast moving and dynamic environment to join our Custom Solutions Team! The Biochemist I will be an integral member of a team, that manufactures and provides purified antibodies to enable studies for novel applications in precision medicine, oncology, immunology, neuroscience, and stem cell research. This position will report to a team lead and will ensure the highest quality of our finalized antibody products. This is a great opportunity to work in a fast-paced and dynamic environment for you to enhance your knowledge in the biotechnology industry! In this position you will manufacture custom purified antibodies under ISO13485 standards, troubleshoot problematic errors, continue to improve methodologies for efficiency, follow Standard Operating Procedures (SOP)s, and cross train on a variety of other supporting tasks. | 3/23/2023 |
| 5020 | BioLegend San Diego, CA Research Associate - Recombinant Protein & Molecular Cloning BS in biological sciences. Exp: 1-3 years |
This position is responsible for developing cutting edge recombinant protein research products in Molecular Cellular Biology group. The research associate will be involved on developing a new line of recombinant protein products by supporting other team members. The duties include preparing buffer solutions and cell culture media, performing PCR and DNA purification according to standard operating procedures, performing bacterial and mammalian cells cultures, and purifying recombinant proteins with affinity tag. This position offers a significant opportunity for learning molecular biology techniques and career growth in the biotechnology industry. | 3/23/2023 |
| 5021 | Bio-Rad Woodinville, WA Production Chemist I Bachelor’s degree in a life science or related field. Science knowledge to include Chemistry and Biology, Exp: 1-3 years |
Bio-Rad is looking for a Production Chemist to support our Woodinville Manufacturing Plant working in an FDA/ISO regulated manufacturing lab making reagents to support Bio-Rad’s product lines. In this role, you will be trained on following Material Batch Records for creating an array of buffers, diluents, conjugates, positive controls and negative controls. You will work with a small team to meet Bio-Rad’s production needs and assist in lab upkeep. | 3/23/2023 |
| 5022 | Bio-Rad Woodinville, WA Production Chemist I BS/BA Degree in the life science or related field. Exp: 1-3 years |
As a BioPlex Production Chemist, you will be part of a Team that supports Bio-Rad’s commitment to quality and safety. You will apply your science knowledge – and build on it - by formulating the various reagents for the BioPlex2200 Kits. This is accomplished according to FDA/ISO regulated manufacturing and per document methods employing Good Laboratory & Manufacturing Practices. This role is critical in maintaining the overall quality of Bio-Rad’s products and services. | 3/23/2023 |
| 5023 | Bio-Rad Woodinville, WA Quality Control Spec I BS/BA degree in the physical sciences. Exp: 1-3 years |
Bio-Rad is looking for a Quality Control Specialist to support Bio-Rad’s commitment to quality and safety by testing raw material and in-process commercial Quality Control testing. As a part of our Quality Control team, you’ll apply your science knowledge in testing BioPlex for assay component raw materials, bulks, fills and finished kits tested according to FDA/ISO regulated manufacturing employing Good Laboratory & Manufacturing Practices. This role is critical in maintaining the overall quality of Bio-Rad’s products and services. | 3/23/2023 |
| 5024 | Bio-Rad Irvine, CA Quality Control Spec I Bachelor's degree, or equivalent, in a life science or related field. Exp: 0-2 years |
Job requires Raw Material/Intermediate inspection & testing. Perform sampling and physical testing of raw materials as described in the documented procedures. Ensure documentation is accurate and revise as needed. Recognize and investigate out of specification results, out of trend results and report to supervisor. Assist with method correlation and other job-related tasks as required. Enter results into SAP & Laboratory Information Management System (LIMS) as required. Follow good laboratory practices & procedures. Work in a team environment & interface with other departments as required. | 3/23/2023 |
| 5025 | BioReference Laboratories Elmwood Park, NJ Medical Technologist (FT, 40 Hours) Bachelor of Science Degree in Medical Technology, Chemistry, Biology, or Related life Science. One or more years of CLIA experience. Required for tech Exp: One or more years |
The Medical Tech performs all laboratory procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. | 3/23/2023 |
| 5026 | BioReference Laboratories Melbourne, FL Medical Laboratory Technologist (FT, 40 Hours) Bachelor of Science Degree in Medical Technology, Chemistry, Biology, or Related life Science. One or more years of CLIA experience. Required for tech Exp: One or more years |
The Medical Tech performs all laboratory procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. | 3/23/2023 |
| 5027 | BioReliance Rockville, MD Associate Scientist 2 - 2nd Shift Bachelor’s Degree in a scientific discipline (e.g., Biology, Chemistry, Microbiology, etc. ) Exp: 1+ years |
At MilliporeSigma, as an Associate Scientist 2 – 2nd Shift , you will perform assays and safety testing required to manufacture clinical and commercial products. You will make scientific observations, maintain detailed workbooks/documentation, and ensure all documentation fulfills generally accepted professional/industry standards. | 3/23/2023 |
| 5028 | BioReliance Temecula, CA Scientist I - Organoid Culture And Characterization Master’s Degree in Chemical Engineering, Biochemical Engineering, Cell Biology, Biochemistry, or other life science discipline. Exp: 1+ years |
Help identify, evaluate, and design new protocols for human organoid development Culture and Passage organoids under sterile conditions Characterize organoids using techniques like QPCR, RNA Seq, Confocal microscopy etc. Follow product development plan to create commercial products from PDOs and SCOs Develop key biological assays using PDOs and SCOs Train other lab members in new/ advanced techniques Lead technology transfer and training of manufacturing personnel Prepare technical data packets for commercial use Help develop relevant reagents for PDOs or other organoids Engage with internal/ external collaborators and customers as technical champion for PDOs Leverage specialized knowledge and analytical skills to solve complex problems Summarize and present experimental results in written and oral reports Present the company at international conferences/ webinars to promote our brand awarenes | 3/23/2023 |
| 5029 | BioReliance Indianapolis, IN QC Analyst I Bachelor’s Degree in Chemistry, Biochemistry, Organic Chemistry, or other scientific discipline. Exp: 1+ years’ |
The QC Analyst I is a technical entry-level position responsible for analytical testing of finished product, raw materials, stability and special test requests. This position also requires analytical testing in support of protocols related to method transfers, method validations, laboratory investigations, and instrument qualifications. | 3/23/2023 |
| 5030 | BioReliance Milwaukee, WI Scientist Production Associate - 2nd Shift Bachelor’s Degree in Chemistry or Chemical Engineering Exp: 1+ years |
An Associate Production Scientist will assemble, operate, clean, and disassemble complete flow chemistry equipment according to established procedures and following safety protocols. You will annotate completed steps and processes in batch records in accordance with good documentation practices. You will test in-process samples using GC, Karl-Fisher titration, HPLC, 1H NMR spectroscopy, and FTIR spectroscopy. You will lead innovation projects designed to improve processes and reduce costs. You will have a passion for producing quality products that meet our customers’ needs and expectations. This is a 2nd shift position, Monday - Friday 2pm - 10:30pm. | 3/23/2023 |
| 5031 | BioReliance St. Louis, MO CGMP Associate Production Scientist Bachelor’s Degree in Chemistry, Biochemistry, Chemical Engineering, or other life science discipline Exp: 1+ year |
The Associate Production Scientist at MilliporeSigma is responsible for the manufacturing of active biopharmaceutical ingredients (APIs) Chemicals and bulk pharmaceuticals regulated by the Food and Drug Administration (FDA). The Associate Scientist is responsible for following manufacturing protocols, consistent with and established according to current Good Manufacturing Practices (cGMP) and ensuring the accuracy of documentation. 12-hour overnight shift (6pm-630am) Two-week rotation: Week 1 (Monday/Tuesday/Friday/Saturday) Week 2 (Sunday/Wednesday/Thursday) | 3/23/2023 |
| 5032 | BioReliance Indianapolis, IN Process Engineer Bachelor’s Degree in Chemical Engineering or Biochemical Engineering Exp: 1+ years’ |
As Process Engineer, you will be responsible for providing key engineering support and project coordination to all phases of plant operations. The Process Engineer is also responsible for interfacing with internal and external clients in support of product technology transfers and manufacture, as well as providing technical support for processes and product investigations. | 3/23/2023 |
| 5033 | Bio-techne San Jose, CA Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
Salary Range: $71,400 – 107,000 depending on experience and qualifications Are you awesome? Come join an awesome team, doing amazing science! Bio-Techne develops, manufactures, and sells innovative tools and high-quality reagent solutions for life science research, therapeutic manufacturing, and clinical diagnostics. Among the Bio-Techne brands is ProteinSimple, a company based in San Jose, CA, that manufactures innovative analytical instrumentation. ProteinSimple is home to the Applications Science Team, a team generating amazing new applications and content, leading impactful and often game-changing collaborations with key customers, key customer support, and fee-for-service custom method development. The Applications Science team is seeking a highly motivated Advanced Research Associate to join our ranks! In this position, you will work daily with innovative analytical platforms on cutting edge research areas alongside our scientists to contribute exciting data for scientific collateral and custom projects. | 3/23/2023 |
| 5034 | Bioventus Memphis, TN Quality Engineer I Bachelor’s degree in Engineering or Science discipline or equivalent technical field. Exp: Up to 2 years’ |
The Quality Engineer I provides Quality Engineering support to Manufacturing, Engineering, QC/QA, and Process Development and IT teams to ensure that products are manufactured with a high level of quality, while being in compliance with regulations governing medical device manufacturing. | 3/23/2023 |
| 5035 | BioVision Waltham, MA Senior Research Associate, Cell Engineering Master Degree in Life Science Exp: 0+ years |
We are seeking a Senior Research Associate to join our Waltham, MA team to provide cell culture support for both the high throughput workflow for KO cell line generation and the preparation and replenishment of these KO cell banks for internal and external customers. This is predominately a benchwork lab-based role and your daily activities will contribute directly to Abcam’s goals and values. | 3/24/2023 |
| 5036 | Blueprint Medicines Cambridge, MA Senior Research Associate, Biology BS in in cell/molecular biology, cancer biology, genetics or related field Exp: 1-3 years |
We are seeking a highly self-motivated research associate to join a team of scientists working towards the discovery of novel anti-cancer drugs for the treatment of targeted patient populations. | 3/24/2023 |
| 5037 | Cambrex Agawam, MA Clean Room Analyst - Microbiological Environmental Monitoring Bachelor’s degree or higher in Microbiology or related field. Exp: 12 months |
As a Cleanroom Services Analyst you will perform environmental monitoring and cleanroom qualifications using within controlled environments. You will travel to regional client sites to provide your expertise with equipment, procedures, policies and regulations to ensure that their cleanrooms meet the requirements for safe manufacturing of medical devices, pharmaceuticals and other patient products. | 3/24/2023 |
| 5038 | Cambrex Marlborough, MA Clean Room Analyst - Microbiological Environmental Monitoring Bachelor’s degree or higher in Microbiology or related field. Exp: 12 months |
As a Cleanroom Services Analyst you will perform environmental monitoring and cleanroom qualifications using within controlled environments. You will travel to regional client sites to provide your expertise with equipment, procedures, policies and regulations to ensure that their cleanrooms meet the requirements for safe manufacturing of medical devices, pharmaceuticals and other patient products. | 3/24/2023 |
| 5039 | Aimmune Therapeutics Leonia, NJ Laboratory Tech - 1st Shift Bachelor of Science degree preferred. Exp: 0 - 3 years |
Under the direction of the QC Laboratory Supervisor, the Lab Technician is responsible for performing routine laboratory support functions, cleaning of glassware and general housekeeping. Non-routine duties are performed in a learning capacity under direct supervision. Responsibilities are focused on less complex testing and support functions. | 3/14/2023 |
| 5040 | Aimmune Therapeutics Leonia, NJ Technical Services Scientist Bachelor’s Degree in Chemistry, Chemical Engineering, Pharmaceutical Science or other related discipline is preferred. Exp: 1-3 years' |
Under the direction of the Tech Services Manager, the CTAG Specialist - Solid Dose will work closely with multifunctional teams to help improve current products, address manufacturing issues, evaluate new technologies and/or ingredients, seek cost savings and maintain networks of external partners. Adherence to Standard Operating Procedures (SOP’s) and current Good Manufacturing Practices (cGMP’s) is required. | 3/14/2023 |
| 5041 | Aimmune Therapeutics Bohemia, NY Associate Chemist (Junior) Bachelor's degree in chemistry, biology, or a related science field Exp: 1 – 2 years |
The Associate Chemist applies knowledge and skills to perform diverse and complex laboratory procedures and /or specialized technical, administrative services requiring application of equivalent technical knowledge in a quality control laboratory. Also, responsible for adhering to the Standard Operating Procedures (SOPs) and Good Manufacturing Practices (cGMPs) that are in effect assuring the quality and quantity of product produced. | 3/14/2023 |
| 5042 | Aimmune Therapeutics Bohemia, NY Associate Chemist (Junior) Bachelor's degree in chemistry, biology, or a related science field Exp: 1 – 2 years |
The Associate Chemist applies knowledge and skills to perform diverse and complex laboratory procedures and /or specialized technical, administrative services requiring application of equivalent technical knowledge in a quality control laboratory. Also, responsible for adhering to the Standard Operating Procedures (SOPs) and Good Manufacturing Practices (cGMPs) that are in effect assuring the quality and quantity of product produced. | 3/14/2023 |
| 5043 | Akadeum Life Sciences Ann Arbor, MI Production Support Chemist Bachelor’s degree in the life sciences Exp: 1 - 3 years |
Akadeum is seeking a Production Support Chemist with an early-stage mindset who will help manufacture kits and materials to support customers and partnerships, following standard operations procedures under a quality system. In your role, you will also help with shipping and support R&D material requests as needed. The role may include other duties as required to support company growth and operations. You will bring outstanding communication skills, a very high level of attention to detail, and an enjoyment of processes. You enjoy following established procedures, along with taking pride in delivering high quality products to researchers. Being highly motivated to produce disruptive technology under timelines and comfortable working in a fast-paced setting both as part of a team and independently is also important. | 3/15/2023 |
| 5044 | Akoya Biosciences Marlborough, MA Quality Engineer Bachelor’s Degree in Engineering or technical discipline Exp: 1-3 years |
Akoya Biosciences is looking for a Quality Engineer to join our Quality team. Reporting to the Supplier Quality Engineering Manager, this individual will manage a variety of quality system functions of Akoya Biosciences’ growing Quality Management System (QMS), working with Quality Management, product development, manufacturing, supply chain, and other groups, to ensure compliance to ISO 13485 and medical device quality requirements. The individual must be able to work independently and resolve or escalate quality issues in a creative, collaborative, and timely manner. Core values must include commitment to customer and operations excellence with demonstrated ethics and integrity. The Quality Engineer will manage day-to-day QMS processes such as monitoring & measuring supplier performance, auditing, validation planning, change control, CAPA, complaint & nonconformance investigations, and design quality. The individual will also help to develop new processes as the QMS grows and will have opportunities to grow within the Quality group. | 3/15/2023 |
| 5045 | Akron Biotechnology Sarasota, FL Technician, Quality Control BS in Biology, Chemistry or related science discipline. Exp: 1 or more years |
Akron Biotech is continuing to transform and further its rapidly growing capabilities and is now seeking highly motivated professionals to join our expanding team. This is an exciting opportunity to play a critical role within our organization that is driving advanced therapy development and commercialization with high quality industrial scale solutions. We manufacture and distribute components and raw materials for cell therapy discovery, development, and commercialization to meet industry needs worldwide. We offer an array of highly competitive benefits and perks to our valued associates. | 3/15/2023 |
| 5046 | Allakos San Carlos, CA Research Associate/Senior Research Associate, Protein Biochemistry B.S. or M.S. in Biological Sciences or related discipline Exp: 1-3 years |
Allakos is a clinical stage company focused on developing therapeutic antibodies against inhibitory receptors expressed on key immune cells involved in allergic, inflammatory, and proliferative diseases. We are seeking a highly motivated Research Associate/Senior Research Associate with a strong background in protein biochemistry to join our R&D team. The selected candidate will be responsible for generating different types of proteins to support our lead and pre-clinical antibody programs. This position will provide the candidate an opportunity to perform a wide range of activities and expand/learn new techniques across the Protein Sciences Team. | 3/15/2023 |
| 5047 | AllCells Alameda, CA Laboratory Associate - CGT Bachelor’s degree in Life Sciences. Exp: 1 year |
The Laboratory Associate is responsible for processing and isolating human primary cells and conducting quality control analysis. | 3/15/2023 |
| 5048 | AllCells Woburn, MA Laboratory Technician- Woburn, Mass. Bachelor of Science degree with a focus in Biology, Chemistry, (or related field) Exp: 1+ years |
Discovery Life Sciences is a trusted provider of bioanalytic and biospecimen services to hundreds of customers across the U.S. and around the world. The Laboratory Technician/Scientist in this manufacturing environment, produces materials and enzymes that feed the manufacture of hepatocyte-related products. This Technician works with animal and human tissue and manufactures enzyme based products. This position will work on-site in Woburn, Massachusetts. | 3/15/2023 |
| 5049 | AllCells Newtown, PA Histology Technologist Master's degree in a laboratory science (i.e. biology, chemistry, or other lab science) Exp: We provide training |
Discovery Life Sciences is a specialty laboratory services provider at the forefront of using IHC as a biomarker platform for personalized medicine. With our expertise in IHC services focused on oncology, inflammatory diseases, as well as other disease states, we are developing novel cancer tests to improve cancer patient outcomes. The Histology Technologist contributes to our mission by supporting the Study Director throughout the duration of a project including sponsor and study director updates, developing study design, assisting with proposal writing, and presenting to clients. | 3/15/2023 |
| 5050 | AllCells Huntsville, AL Associate Scientist - Flow Cytometry BS in Biology, Chemistry, Biochemistry, Immunology, or related discipline. Exp: 1-2 years |
Discovery Life Sciences is a globally recognized contract services laboratory that leverages the most current technologies to comprehensively support discovery, translational, and clinical research for the Pharmaceutical, Biotechnology and Diagnostic industry as well as Academic and Research Institutes. The successful candidate will help build testing pipeline, support validation efforts, and execute clinical flow cytometry testing in clinical trials studies. This role will be important in the continued growth of Flow Cytometry within the company with an opportunity to work and grow in a fast-paced environment and make an impactful contribution to the growth of Discovery Life Sciences. | 3/15/2023 |
| 5051 | AllCells Huntsville, AL Histology Technician Bachelor's Degree Required Exp: one year |
Previous knowledge of Histology or Pathology and a scientific background is a plus. The Histology Technician will coordinate and support the work of our growing Pathology Team through our Whole Slide Imaging digital platform. These duties require the ability to communicate clearly with internal or external contacts, either verbally or in writing. The DLS FFPE laboratory is a fast-paced environment that requires a focus and a commitment to always do the job correctly because the work we do impacts research worldwide. Discovery’s quality samples offer our clients the greatest opportunity to develop new treatments and diagnostics for patients suffering from a variety of diseases. We work every day because these patients are waiting. | 3/15/2023 |
| 5052 | Alliance Pharma Malvern, PA Assistant Scientist II BA/BS or higher Exp: 1-2 years |
Performs routine lab work, sample analysis, and validation under limited supervision. | 3/16/2023 |
| 5053 | ALPCO Diagnostics Salem, NH Reagent Chemistry Associate Bachelor’s degree in the Sciences (preferably in Chemistry or Biology). Exp: 1 - 3 years |
The Reagent Chemistry Associate works under general supervision and is expected to follow established procedures in the manufacture of ELISA kits and components; can perform standard manufacturing procedures and has knowledge of commonly used laboratory concepts and practices; relies on instructions and established guidelines or protocols to perform job functions; self stater who can work under minimal supervision. | 3/16/2023 |
| 5054 | Alstem Richmond, CA Research Associate B.S. or M.S. degree in Biochemistry, Molecular Biology or related discipline. Exp: 1 year |
ALSTEM, INC is a growing research biotechnology company located in Richmond, CA. ALSTEM is a nimble provider of tools specializing in virus packaging, genome editing, cell engineering and stem cells for life science research. ALSTEM is looking for a highly organized and energetic Research Associate with a B.S or M.S. degree to join its scientific team. The candidate will be responsible to work as a team at all levels which will include but will not be limited to product testing and QC, and custom service projects following SOPs and protocols to support customer workflows. | 3/16/2023 |
| 5055 | Norwich Pharmaceuticals Norwich, NY Quality Systems Specialist I Bachelor of Science in Chemistry, Life Science, Engineering Exp: 1 - 3 years |
The Quality Systems Specialist provides system administration and support of daily quality activities to ensure compliance with global regulatory requirements and guidelines (FDA, ICH, EU, WHO, etc.). | 3/16/2023 |
| 5056 | Amarex Clinical Research Ann Arbor, MI Technician II - Extractions Lab 2 year degree – Science Degree Exp: 1-5 years |
NSF International is currently has an opening for a Technician II – Extractions Lab to support the extractions staff. This lab is crucial in prepping samples from NSF's Prep Labs before sending the samples off to NSF's analytical laboratories. In this position, a candidate would use high attention to detail to perform extractions of water samples. | 3/16/2023 |
| 5057 | Amarex Clinical Research Ypsilanti, MI Engineering Lab Technician Bachelor or Associate degree in an Engineering or Scientific discipline Exp: One year |
As a Technician II for Engineering/Plastics, you will be responsible for conducting basic testing on plastics, pipes, fittings and other related plumbing products to specific standards and procedures. | 3/16/2023 |
| 5058 | AmbioPharm North Augusta, SC Microbiologist BS in Microbiology or life sciences. Exp: 1-5 years |
Perform procurement and testing of: city and pharmaceutical grade water per USP guidelines and SOP; product for bioburden, endotoxin per USP guidelines and SOP; stability samples per SOP; environmental monitoring sample (viable and non-viable) per USP guidelines and SOP, as scheduled (daily, weekly, monthly, quarterly) Support production in qualification of clean rooms and water systems. Data entry for trending reports Perform QC testing and release of microbiological media, reagents, and stock cultures Maintenance of stock cultures Use of aseptic technique for sampling and testing of all samples collected for microbiological analysis Documentation of all activities per current good documentation practices as described in SOP Use basic understanding of and knowledge of techniques, instrumentation and lab functions to identify problems, initiate investigations and support completion of work assignments Maintain inventory and ordering of supplies, media, reagents and stock cultures used in routine testing Support test method development and qualification/validation studies | 3/16/2023 |
| 5059 | AmbioPharm North Augusta, SC QC Chemist II Masters Degree in Chemistry or life sciences Exp: 1-2 years |
Use basic understanding and knowledge of techniques, instrumentation, and lab functions to identify problems and support the completion of work assignments. Hands on experience with HPLC, GC, IC, KF and other routine analytical equipment such as pH meter and balance. Perform quality control routine testing for raw material/ Intermediate/ Release / Stability testing Perform Method development and method validation execution, including writing protocols and reports. Must be proficient. Responsible for reviewing analytical laboratory raw data and electronic records. Participate in out of specification (OOS) investigations, as well as other deviations and writing investigation reports. Perform and review QC stability and release testing. Maintain the QC lab by ordering supplies routinely used for testing. Assist the QC/QA group with writing and editing of SOPs and STPs. Other duties as assigned. | 3/16/2023 |
| 5060 | AmbioPharm North Augusta, SC Purification Chemist I Bachelor of Science in Chemistry or equivalent Exp: 1-3 years |
Work in a cGMP environment to perform the peptide purification processes through chromatography as well as other various purification techniques. Use analytical skills to prevent and solve possible process complications and problems. Work as part of a team to complete specific projects in a timely manner. Follow approved cGMP manufacturing directions such as production batch records, standard operation procedures and standard test procedures. Help the team to install, test, operate and maintain equipment for manufacturing and in-process testing. Help the team to investigate any process deviation. Write deviation reports and initiate document change requests. Monitor compliance of maintenance and cleaning procedures of equipment and instruments used in GMP processes by periodically reviewing and signing off on maintenance and cleaning logs for each equipment. Help QC and QA departments to maintain the equipment calibration program. Must be willing to work rotating shifts and weekends. | 3/16/2023 |
| 5061 | AnaSpec Fremont, CA Synthesis Chemist I BS or above in Chemistry, Organic Chemistry, or related disciplines Exp: 1-3 years |
The Synthesis Chemist I will perform peptide production and conduct in-process testing using Good Laboratory Practices (GLP). As a member of the Synthesis department, the Synthesis Chemist I will work closely with the Purification, QC, and Sales & Business Development departments. | 3/16/2023 |
| 5062 | Anika Therapeutics Bedford, MA QA Compliance Specialist I Bachelor’s Degree or relevant experience in the life sciences. Exp: 1-2 years |
The Quality Assurance (QA) Compliance Specialist I performs compliance activities in support of production, engineering ensuring all activities are performed according to internal Quality System requirements, cGMP, FDA and ISO 13485 standards. Areas of responsibilities include receipt and review of documents such as charts, logs, batch records and approval of incoming materials for release. The position will provide floor support to production departments to include line clearances, in-process checks and assistance with investigations. The QA Compliance Specialist I performs quarterly audits support internal audits and participates in customer and regulatory audits as part of the Audit Team. | 3/16/2023 |
| 5063 | ANI Pharmaceuticals Baudette, MN QC Chemist/Sr. QC Chemist Bachelors degree in chemistry, biochemistry, microbiology or closely related field/major. Exp: QC Chemist – 1-3 years |
The QC Chemist position is responsible for independently performing testing in a pharmaceutical Quality Control laboratory. All work will be conducted in accordance with standard operating procedures and test methods. This includes performing testing on raw material, in-process and finished product samples. Execute compendia method validations, method transfers and validation support of new product development. Set up and confirm suitable operation of equipment and instrumentation. Collect data and generate/report results in accordance with governing test methods and SOPs. | 3/16/2023 |
| 5064 | Applied StemCell Milpitas, CA R&D Research Associate Master’s degree in Biochemistry, Cell Biology, or a closely related field. Exp: 18 months |
Support in vitro and in vivo gene editing applications, including molecular biology and cell work, for research and proprietary therapeutic technologies. Maintain the FACS (Flow Cytometry) equipment on a regular basis, perform daily quality control measurements, and initiate corrective actions in case of instrument failures. As directed, perform protein assay techniques, molecular cloning experiments, genotyping experiments, and ad nucleic acid isolation. Set up, operate, and maintain laboratory instruments and equipment, monitor experiments, collect data and samples, make observations, and calculate and record results. Analyze organic substances. Conduct research, and assist in the research, including the collection of information and samples, such as blood and animal tissues. Use computers, computer-interfaced equipment, robotics, and high-technology industrial applications to perform experiments and examinations. Monitor and observe experiments, recording production and test data for evaluation by research personnel. Analyze experimental data and interpret results to write reports and summaries of findings. Provide technical support and services for scientists and engineers working on employer’s proprietary genome editing and stem cell technologies. | 3/16/2023 |
| 5065 | Aquinnah Pharmaceuticals Cambridge, MA Research Associate Master’s degree in neuroscience, cell biology or related discipline Exp: 1+ years |
This position is laboratory-based and requires strong experimental skills with a background in cell biology, molecular biology, or biochemistry. Under supervision, the candidate will assist in duties including, but not limited to: cell culture maintenance, compound screening, biochemical assays, immunocytochemistry, and analysis using state of the art high-content imaging. Strong communication skills are required including the ability to analyze and report on the results. The candidate will be expected to function efficiently and cooperatively within a team and maintain accurate and clear project records. The ideal candidate will be creative, energetic and motivated. | 3/17/2023 |
| 5066 | Arraystar Rockville, MD Lab Assistant - Molecular Biology Bachelor’s degree in a relevant biological field. Exp: 1-2 years’ |
Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. Assist with the generation and updating of laboratory SOPs. | 3/17/2023 |
| 5067 | Arvinas New Haven, CT Research Associate, Formulation R&D Bachelors of Science degree in a physical science. Exp: 1-2 years |
In the role as a Research Associate, you will prepare pharmaceutical formulations used in animal pharmacology and pharmacokinetic studies, and will work closely with compound management and in-life colleagues to make sure that dosing materials are available as needed. When issues related to formulation arise, you will serve as a primary problem-solving Formulation R&D contact for those in other disciplines. You will be responsible for ordering necessary excipients so that the animal studies will start on time and be comfortable dealing with last-minute scheduling changes. This position reports to the Research Scientist, Technical Operations and will be located at our headquarters in New Haven, CT. | 3/17/2023 |
| 5068 | Astute Medical Salt Lake City, UT Research Associate I Bachelor’s degree with an emphasis in science. Exp: entry-level |
The Molecular Biology Research and Development Department is seeking a research associate to work with department scientists and staff on the design, development, verification, and technical support of molecular in vitro diagnostic products for infectious diseases. The Research Associate I is a technical, hourly position with laboratory responsibilities. The RA I works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g. nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to effectively and respectfully communicate and coordinate with peers and supervisor(s). The position requires basic proficiency in laboratory technical and organizational skills, attention to detail, critical thinking, troubleshooting and problem-solving, data analysis, sequence analysis, and a dedication to the mission and goals of the department and bioMerieux. A Research Associate I will work collaboratively with other Research Associates, self-direct on routine work with no or minimal instruction and supervision, and will operate with general or detailed instruction and supervision on new procedures and assignments. | 3/17/2023 |
| 5069 | Astute Medical Salt Lake City, UT Research Associate I or II B.S. in molecular biology, biology, biomedical sciences, or a related field. Exp: One to two years |
The Molecular Systems Research Associate I or II (RA I/II) position is a full-time, non-exempt position. This position is part of a team working on various laboratory procedures involving nucleic acid isolation methods and PCR under general guidance. This person will work closely with other research associates or scientists in the research lab. | 3/17/2023 |
| 5070 | Astute Medical Salt Lake City, UT Research Associate I Bachelor’s degree in a scientific discipline or equivalent. Exp: 0-2 years |
This is a full-time non-exempt position. This position is part of a team working on a variety of laboratory procedures involving real-time PCR using established methods and techniques under general guidance. This person works closely with other research associates in the department. Performs general lab duties, designs and conducts experiments, collects and analyzes data, and keeps an accurate record of all work done in accordance with the quality system. Requires some problem-solving skills. Normally receives general instructions on routine work and detailed instructions on new assignments. Reports to the Senior Research Associate or Scientist. | 3/17/2023 |
| 5071 | Astute Medical Salt Lake City, UT Research Associate I Bachelor’s degree in a scientific discipline or equivalent. Exp: No experience |
This position is part of a team working on a variety of laboratory procedures involving real-time PCR using established methods and techniques under general guidance. Performs general lab duties, conducts experiments under the supervision of their manager, collects and analyzes data and keeps an accurate record of all work done in accordance with the quality system. Requires some problem solving skills. Normally receives general instructions on routine work, detailed instruction on new assignments. Reports to the Lab Supervisor or a Scientist. This is a full time non-exempt position. | 3/17/2023 |
| 5072 | Astute Medical Salt Lake City, UT Research Associate I Bachelor’s degree in a scientific discipline. Exp: 0-2 years |
The Research Associate I is a technical hourly position with laboratory responsibilities. The RA I works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of FDA and other regulatory submissions. Tasks will focus on molecular and microbiological experiments and procedures (e.g. nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to communicate and coordinate with peers and supervisor(s) effectively and respectfully. The RA I position requires basic laboratory technical and organizational skills, attention to detail, critical thinking, troubleshooting and problem-solving, and a dedication to the mission and goals of the department and BioFire. A Research Associate I may receive general or detailed instruction and supervision on routine work, and detailed instruction and supervision on new procedures and assignments. | 3/17/2023 |
| 5073 | Atreca San Carlos, CA RESEARCH ASSOCIATE/SENIOR RESEARCH ASSOCIATE, HISTOLOGY BS or MS, preferably in biology or related field. Exp: 1-3 years |
In this position, the successful candidate will apply her/his basic science laboratory skills and expertise regarding histological tissue preparation and execution of tissue staining protocols (i.e.immunohistochemistry, immunofluorescence and simple stains) to contribute to Atreca’s antibody-target characterization research. The position reports to the Associate Director of Histopathology. The candidate’s expertise with immunohistochemistry, other histological methods will help us to discover and characterize novel tumor antigens and develop anti-tumor drugs. | 3/17/2023 |
| 5074 | Atreca San Carlos, CA TEMPORARY RESEARCH ASSOCIATE I, ANTIBODY INVENTORY Pursuing or completed Bachelor’s in Life Sciences or Engineering Exp: 1-3 years |
We are seeking an enthusiastic and motivated Research Associate to grow our Antibody Inventory efforts as part of the Protein Engineering group. The successful candidate will help manage and maintain Atreca’s antibody inventory and ensure suitability for downstream assays. This very central position will involve interacting with multiple research teams dedicated to the discovery of novel, antibody-based cancer therapies. | 3/17/2023 |
| 5075 | August Bioservices Nashville, TN Microbiologist I B.A./ B.S in Biology (or related) Exp: 0–2 years |
August Bioservices is looking for a Quality Control team member that is passionate and driven professionally. August Bioservices desires a team member eager to work in an environment where people are motivated to do their best for the company and its clients. Reporting to the Manager, Microbiology, the Microbiologist I will be responsible for performing biological assays of raw materials, in-process samples, finished product, and environmental monitoring samples. He/she will work with microbiology personnel to assure test results, procedures, and methods are written, maintained, executed, and approved in accordance with approved SOPs and regulatory requirements. | 3/17/2023 |
| 5076 | Avalign Technologies Fort Wayne, IN Quality Engineer BS in an engineering science. Exp: 0--3 years |
The Quality Engineer is responsible for supporting the organization to ensure quality and production goals are met. The Quality Engineer will utilize an engineering approach to improve manufacturing efficiencies and ensure quality standards of all products are met. | 3/17/2023 |
| 5077 | Avalign Technologies Greenwood, IN Quality Engineer BS in an engineering science. Exp: 0-3 years |
The Quality Engineer is responsible for supporting the organization to ensure quality and production goals are met. The Quality Engineer will utilize an engineering approach to improve manufacturing efficiencies and ensure quality standards of all products are met. | 3/17/2023 |
| 5078 | Avomeen Boulder, CO Research Technician BS Degree preferred but not required. Exp: 1-3 years |
Element is currently hiring for a Research Technician for our Boulder, CO location. The main responsibility of the Research Technician is to assist the Clinical Study Coordinator in facilitating the Study in each Laboratory in order to meet customer turn time and requests; to help ensure the Studies are performed to protocol(s) requirements; to ensure that the Studies meet requirements of the Quality System. The pay range for this role is between $25/hr.-$40/hr., depending on level of relevant experience. | 3/17/2023 |
| 5079 | Vapotherm Exeter, NH Quality Engineer I B.S. in Engineering or Science, or equivalent technical field. Exp: 0-2 years |
The Quality Engineer will be responsible for representing quality on projects and overall quality support to the organization including implementation of Vapotherm’s Quality Management System. While this role will be primarily focused on new product development, this role will support general sustaining activities as well as maintaining the effectiveness of the overall QMS. | 3/6/2023 |
| 5080 | VaxCyte San Carlos, CA Associate Scientist I, Protein Process Development & Manufacturing BS in Chemical Engineering, Biochemistry, or a related discipline Exp: 0-2 years |
Vaxcyte is looking for a motivated and collaborative individual to join the protein process development team. This is an entry level position, that can lead to a highly impactful career within Vaxcyte. By managing general lab work, generating needed materials for development use, and running assays that generate highly valuable data on process performance, this person can make a significant impact on the development of life-saving vaccines. As a member of the protein development team, this individual will have the opportunity to learn cutting edge technology using cell-free protein expression and Nobel Prize-winning click chemistry. | 3/6/2023 |
| 5081 | Vertical Pharmaceuticals Marietta, GA Analytical Chemist- Osmotica Bachelor's degree in Chemistry, Biochemistry, Biology or related field Exp: 0-2 years |
Description The Analytical Chemist I is responsible for testing of raw materials, in-process materials, and finished products to support release and stability programs. Essential Responsibilities: Perform laboratory tests such as sample extractions, set up and execution of chromatographic methods (HPLC and GC), and dissolution testing. Develops and executes UV, IR and PSD measurements and wet techniques as applied in the Pharmaceutical Analysis/Testing of products and excipients. Executes complex study designs. Executes components of method validation and method transfer projects. Assists with sample handling tasks. Documents laboratory work using laboratory notebooks in a detailed and accurate manner that meets cGMP requirements. Performs other duties as assigned or requested | 3/6/2023 |
| 5082 | VGXI The Woodlands, TX VALIDATION SPECIALIST Bachelor’s Degree or equivalent Exp: one to three years |
Support process and product quality programs including process, testing, and software validation, equipment calibration programs, and process monitoring activities by writing simple verification/validation documents, executing qualification tests, compiling data, drafting summary reports, and reviewing validation documentation to ensure products are manufactured in accordance with applicable regulatory guidelines, manufacturer’s specifications, client’s specifications, and VGXI’s requirements. Review, update and work with various departments to develop SOPs for existing and new equipment / tests / processes. | 3/6/2023 |
| 5083 | VGXI The Woodlands, TX QUALITY ASSURANCE SPECIALIST Bachelor's degree from four-year college or university Exp: 1-3 years |
This position will primarily be responsible for quality assurance and compliance activities related to ensuring that production, testing, and associated documentation meets applicable regulatory and client Requirements. | 3/6/2023 |
| 5084 | VGXI The Woodlands, TX DOWNSTREAM PROCESS TECHNICIAN Bachelor’s or Associate's degree or equivalent from college or technical school Exp: 1-3 years |
Responsible for manufacturing revolutionary clinical and commercial nucleic acid based pharmaceuticals by interfacing with manual and automated production systems and controls in cGMP manufacturing environment while maintaining areas in a state of compliance with internal quality systems. Follows standard operating procedures to operate production equipment for downstream operations. Maintains records, process and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for proficiency in assigned functional area: Downstream Manufacturing. Understands and applies biological, chemical and mechanical principles and techniques. | 3/6/2023 |
| 5085 | VGXI The Woodlands, TX UPSTREAM PROCESS TECHNICIAN Bachelor’s or Associate's degree or equivalent from college or technical school Exp: 1-3 years |
Responsible for manufacturing revolutionary clinical and commercial nucleic acid based pharmaceuticals by interfacing with manual and automated production systems and controls in cGMP manufacturing environment while maintaining areas in a state of compliance with internal quality systems. Follows standard operating procedures to operate production equipment for upstream operations. Maintains records, process and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for proficiency in assigned functional area: Upstream Manufacturing. Understands and applies biological, chemical and mechanical principles and techniques. | 3/6/2023 |
| 5086 | VGXI The Woodlands, TX MICROPROCESS TECHNICIAN Bachelor’s or Associate's degree or equivalent from college or technical school Exp: 1-3 years |
Responsible for manufacturing revolutionary clinical and commercial nucleic acid based pharmaceuticals by interfacing with manual and automated production systems and controls in cGMP manufacturing environment while maintaining areas in a state of compliance with internal quality systems. Follows standard operating procedures to operate production equipment for plasmid manufacturing operations. Maintains records, process and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for proficiency in assigned functional area: Microprocess Manufacturing. Understands and applies biological, chemical and mechanical principles and techniques. | 3/6/2023 |
| 5087 | WaVe Life Sciences Lexington, MA Research Associate, Analytical Characterization/Development, Process Development, Oligonucleotide Chemistry B.S./MS in Analytical Chemistry/Organic Chemistry or related discipline Exp: 1-5 years |
Wave Life Sciences is seeking a highly motivated Analytical Chemist to join its oligonucleotide chemistry team in Lexington, Massachusetts. This is an ideal opportunity for an individual who is interested in cutting edge technologies and who thrives in a team-oriented, fast-paced, cross-disciplinary biotech environment. The candidate will take an active role in the analytical characterization of stereodefined oligonucleotides for discovery and development-related activities. | 3/7/2023 |
| 5088 | Frontage Chicago, IL QA Auditor, GLP BS/BA degree in basic or applied science (biology, chemistry, etc.) Exp: 1-2 years |
Position/Job Summary: The individual in this position supports studies of the safety and/or toxicity of various materials (e.g., pharmaceuticals, chemicals, etc.). The QA Auditor monitors study activities, facilities, equipment, personnel, procedures, and pertinent records to ensure that they satisfy appropriate domestic and international Good Laboratory Practice regulations, customer specifications and the company’s standard operating procedures. | 3/7/2023 |
| 5089 | Frontage Secaucus, NJ Lab Technician Associate or bachelor’s degree in a biomedical discipline or related scientific discipline Exp: 1 year |
Duties: Responsible for working under the guidance of the Lab Manager, Investigators; Management, Study Coordinator and Supervisor, to perform study procedures required in clinical studies conducted on behalf of sponsors at the Frontage Clinical Services. | 3/7/2023 |
| 5090 | Frontage Concord, OH Entry Level Lab Chemist B.S. in a chemistry or related field. Exp: entry level |
This position is for an entry level lab chemist. The ideal candidate will help support studies of preclinical drug development in a GLP environment. | 3/7/2023 |
| 5091 | Frontage Concord, OH Technician (Bioanalytical Scientist) B.S. in Biology, Biochemistry, Chemistry, Pharmacology, or related scientific discipline. Exp: 1-3 years |
Under general supervision, this position is responsible or conducting sample preparation for biological samples in an analytical chemistry laboratory and recording study results and observations. | 3/7/2023 |
| 5092 | Uptake Medical Johnson City, TN ERP Support Analyst - Johnson City, TN (On-Site) Bachelor’s degree in Systems Engineering, Computer Science, Information Technology, or Equivalent Exp: one years’ |
The ERP Support Analyst is the primary point of contact for technical support requests related to business-critical information systems serving as a liaison between functional and technical resources. This position is responsible for testing, troubleshooting, training, and documenting the complete order lifecycle including purchasing, EDI connections, order processing, manufacturing, and order fulfillment through warehouse distribution centers and related ERP tasks on an ongoing basis. Additional responsibilities include systems analysis, project tasks, workflow analysis, and technical communication and problem solving to ensure the systems’ performance meets company leadership and user satisfaction requirements. | 3/7/2023 |
| 5093 | Abbott Westford, MA Quality Engineer Master's degree Exp: 0-2 years |
Abbott Vascular provides innovative, minimally invasive and cost-effective products for treatment of vascular disease. Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents Our location in Westford, MA , currently has an opportunity for a Quality Engineer. | 3/7/2023 |
| 5094 | Abbott Columbus, OH Position Assistant Microbiologist-Microbiology-Columbus Plant- 3rd shift Science related Bachelor’s Degree Exp: 1-3 years |
Our Columbus, OH location is Abbott’s oldest nutrition manufacturing plant in the world. Working here, you’ll feel part of a family – a family of 400 that works together to help nourish the world. | 3/7/2023 |
| 5095 | Abbott San Diego, CA Production Chemist I BA or BS in Chemistry or Biological Sciences Exp: Zero to two years’ |
The position of Production Chemist I is within our Toxicology Business Unit located in San Diego, California. Under close supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP, under the direction of senior staff. This job description will be reviewed periodically and is subject to change by management. | 3/7/2023 |
| 5096 | Abbott San Diego, CA Production Chemist I BA or BS in Chemistry or Biological Sciences Exp: Zero to two years’ |
The position of Production Chemist I is within our Toxicology Business Unit located in San Diego, California. Under close supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP, under the direction of senior staff. This job description will be reviewed periodically and is subject to change by management. | 3/7/2023 |
| 5097 | Abbott San Diego, CA Production Chemist I BA or BS in Chemistry or Biological Sciences Exp: Zero to two years’ |
The position of Production Chemist I is within our Toxicology Business Unit located in San Diego, California. Under close supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP, under the direction of senior staff. This job description will be reviewed periodically and is subject to change by management. | 3/7/2023 |
| 5098 | Abbott San Diego, CA Production Chemist I BA or BS in Chemistry or Biological Sciences Exp: Zero to two years’ |
The position of Production Chemist I is within our Toxicology Business Unit located in San Diego, California. Under close supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP, under the direction of senior staff. This job description will be reviewed periodically and is subject to change by management. | 3/7/2023 |
| 5099 | AbbVie Lake County, IL Associate Scientist II - Physical Analytical Chemistry - Microscopy Master’s Degree or equivalent education Exp: no additional experience. |
Perform routine tasks competently and independently, and generate reliable and consistent results. Analyze and critique results, noting significant deviations. Troubleshoot experiments and instrumentation. Learn and understand new experimental techniques. Demonstrate skill in multiple techniques and appropriately modify protocols, as required, to suit the changing needs of research or development sciences. Place data in proper scientific context by consulting and citing relevant literature. Demonstrate technical proficiency in his/her field. Impact projects predominantly through lab and/or pilot plant based activities. Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable. | 3/7/2023 |
| 5100 | AbbVie North Chicago, IL Associate Scientist II/ Scientist I, Protein Biochemistry MS in molecular biology, biochemistry, biotechnology, or other relevant biological sciences. Exp: 0+ years |
Seeking an experienced research scientist to join our Protein Sciences group at AbbVie's headquarters in the Chicago area. The successful candidate will work in a highly dynamic group to provide protein purification support for a variety of small molecule programs across different therapeutic areas in Discovery Research. The candidate should have protein purification experience and be proficient in all standard bioprocess and AKTA purifier. | 3/7/2023 |
| 5101 | AbbVie North Chicago, IL Associate Scientist II / Scientist I, Genome Biology - Genomics Research Center Associate II requires an MS in Cell, Molecular, or Developmental Biology, Biochemistry, Bioengineering, Immunology or a related life sciences field. Exp: Associate II: no experience |
The group is currently seeking a highly motivated Associate Scientist II / Scientist I to assist in the implementation of new ‘omic’ methodologies (epigenomics, transcriptomics, etc) to address gene function and role of causal variants (coding/ non-coding) supporting our Ophthalmology collaboration. | 3/7/2023 |
| 5102 | AbbVie North Chicago, IL Associate Scientist II / Scientist I, Cell Biology & Imaging Master’s Degree in Cell, Molecular, or Developmental Biology, or a related life sciences field. Exp: Associate II: MS and no experience |
We are seeking a talented and enthusiastic Associate Scientist II / Scientist I with experience in human cell culture and microscopy or high content imaging to support GRC’s growing collaboration with AbbVie’s Ophthalmology therapeutic area. This position will be primarily laboratory-focused and will support high content imaging assay and cellular model development, CRISPR-mediated phenotypic screening, and implementation of cutting-edge technologies to assess gene function and drug mechanism of action. Applicants should have broad laboratory research experience using cell and molecular biology techniques. Open communication and curiosity are essential. The candidate is expected to operate in a fast-paced, multi-disciplinary setting and must be able to execute multiple research projects in parallel.We are seeking a talented and enthusiastic Associate Scientist II / Scientist I with experience in human cell culture and microscopy or high content imaging to support GRC’s growing collaboration with AbbVie’s Ophthalmology therapeutic area. This position will be primarily laboratory-focused and will support high content imaging assay and cellular model development, CRISPR-mediated phenotypic screening, and implementation of cutting-edge technologies to assess gene function and drug mechanism of action. | 3/7/2023 |
| 5103 | AbbVie Worcester, MA Associate Scientist, Discovery Biologics BS or MS in Biology or related field Exp: BS: 0-5+ years; MS: 0-2+ years |
Biologics Discovery Sciences at AbbVie is seeking a highly motivated research scientist to join a dynamic team supporting biologics drug discovery. This position will impact projects through purification and characterization of biopharmaceutical products such as monoclonal antibodies in high throughput. The ideal candidate should have direct experience with mammalian tissue culture, protein purification, proficiency in standard chromatography techniques, protein characterization (e.g., MS, SEC), and binding assays (e.g., ELISA and flow cytometry). The applicant should be able to analyze, document, and report data. They should possess excellent communication skills and be comfortable presenting in group settings. | 3/7/2023 |
| 5104 | AbbVie Wyandotte, MI Associate Scientist, Chemistry I Bachelor’s Degree, or equivalent education. Exp: 0+ years |
Generate and analyze precise, reliable, and reproducible data in a timely manner, under the direction of a more senior scientific leader. Demonstrate experimental precision and should possess general understanding of core discipline. | 3/7/2023 |
| 5105 | Allergan Irvine, CA Associate Scientist II - In Vivo Master’s Degree or equivalent education Exp: no additional experience. |
Allergan Aesthetics Biological Research is seeking a highly motivated and innovative candidate who will contribute to multi-disciplinary research in a highly collaborative environment. The successful candidate will support projects aimed at pharmacological characterization of protein-based therapeutics. Under supervision by senior personnel, he/she will carry out a variety of in vivo pharmacological and behavioral assays to characterize and evaluate molecules of interest in rodent models. The candidate will participate in the design of research studies and independently generate precise, reliable, and reproducible data in a timely manner. He/she will demonstrate experimental precision, strong data analysis and interpretation skills, and excellent verbal and written communication ability. | 3/7/2023 |
| 5106 | Abeona Therapeutics Cleveland, OH Associate, Quality Control BS in biochemistry, biology, microbiology, molecular biology or other relevant discipline Exp: 0 to 4 years |
The Quality Control Associate performs routine laboratory activities in support of GMP testing for Quality Control. Testing includes raw material, packaging components, environmental monitoring, in-process and finished product. Interacts with employees internal and external to Quality Control. | 3/8/2023 |
| 5107 | Abveris Quincy, MA Research Associate: Protein Analytics Bachelor’s or Master’s degree in a scientific discipline required (Biology, Biochemistry, Biochemical Engineering) Exp: 1-3 years |
We are seeking a motivated individual to join our team and expand our bioanalytical department. Using state-of-the art technologies and workflows, this Research Associate would work with the Protein Analytics team to ensure project-specific deliverables are met across a diverse panel of discovery campaigns. The role would involve wet lab experimental design, execution, and data analysis for multiple custom antibody development projects incorporating various biologics assay formats. | 3/8/2023 |
| 5108 | Acell Irvine, CA ENGINEER II, PRODUCT DEVELOPMENT M.S. in engineering or scientific discipline Exp: 0-2 years |
The Engineer II, Product Development will participate in projects of varying scope and complexity across Integra with a focus on neurological access and therapeutic devices. The Engineer II, Product Development will be responsible for the mechanical design and assembly of a project, assisting and leading cross-functional teams through some or all phases of the product development process under the guidance of senior engineering and leadership. | 3/8/2023 |
| 5109 | Adaptimmune Therapeutics Philadelphia, PA Manufacturing Cell Therapy Specialist (1st and 2nd shift) Bachelor degree in a cell biology, bioengineering or medical technology related field. Exp: 1+ years’ |
This role will provide support for the manufacturing of gene modified autologous T-cell product at our manufacturing site in the Philadelphia Navy Yard. The Specialist will perform cell processing activities, media formulation, product sampling, and other manufacturing needs as necessary, commensurate with the level of training and experience of employee. Work is primarily in Grade B and Grade C aseptic manufacturing environment, but may also include support of process development runs in the Manufacturing Science and Technology laboratory. | 3/8/2023 |
| 5110 | Adare Pharmaceuticals Vandalia, OH QC Chemist I Bachelor’s degree in Chemistry or closely related field Exp: 0-2 years' |
The QC Analyst is an essential part of the lab Quality team and will be expected to perform physical and chemical testing of intermediate and finished products according to written procedures. | 3/8/2023 |
| 5111 | Adicet Bio Redwood City, CA Manufacturing Associate II / III - Cell Therapy Bachelor’s degree in a biological science, engineering or related science discipline Exp: 1-3 years |
We are seeking a highly motivated and experienced individual with a strong background in cell process development/manufacturing. The Manufacturing Associate 2 will report to the Director of Manufacturing. In this role you will support the daily manufacturing operations of allogeneic CAR T cell therapies, assist with troubleshooting complex and non-routine equipment events, initiate and support deviations, and author SOPs. You will implement Good Manufacturing Practices and best practices to streamline manufacturing operations. You will demonstrate expertise and breadth of knowledge in executing processes across a variety of production activities such as cell processing, aseptic behavior, monitoring equipment and processes, product sampling, and conducting routine sanitization tasks to maintain facility and equipment. You will read and follow defined SOPs and policies, work independently on basic manufacturing tasks, identify, and communicate non-routine events, and review more complex decisions with your direct supervisor. | 3/8/2023 |
| 5112 | Adicet Bio Redwood City, CA Research Associate, RESEARCH: T CELL IMMUNOLOGY, CAR T CELL BS or MS/MSc in biological sciences or a related field. Exp: 1 to 3 years |
We are seeking a highly motivated candidate with a background in immunology to join the Adicet Research Team. The ideal candidate will have in-depth knowledge of T cell immunology and CAR-T cell development. The candidate will work as a part of a multidisciplinary team, utilizing the latest technologies for cell engineering and contributing to the generation of novel cell-based therapeutics for the treatment of cancer. | 3/9/2023 |
| 5113 | Adicet Bio Redwood City, CA Research Associate / Senior Research Associate, Upstream Viral Vector Group Master’s degree Exp: 1 year |
We are currently seeking a highly motivated Research Associate / Senior Research Associate with previous cell culture experience to assist in executing upstream operations for production of viral vectors. The successful candidate will join Upstream Viral Vector Team and contribute to the advancement of Adicet’s vector production platforms by set-up and maintenance of various cell cultures in adherent and suspension systems. The position also provides the opportunity to learn downstream processing procedures through interactions within the Viral Vector Development Team. The ideal candidate will work in collaboration with other Viral Vector scientists, as well as other cross-functional teams, to support the development of Upstream culture processes, help facilitate tech transfer to internal and external groups, and contribute to development of a best-in-class vector manufacturing process. This person will also work with other internal and external functional groups to help meet developmental timelines and continuity of manufacturing operations. This person would be a contributor to the Vector Team’s objectives in meeting project timelines, achievement of cooperate goals, and delivery of a consistent and robust viral vector product. | 3/9/2023 |
| 5114 | Adimab Lebanon, NH Research Associate - Sequencing B.S. in molecular biology, biochemistry, or a related field Exp: Entry Level |
We are seeking a skilled molecular biologist to join our team. This position will support Adimab's novel antibody discovery, maturation, and production platform by contributing to the sequencing core, performing core laboratory services, and taking on other responsibilities that may arise at a growing biotech company. | 3/9/2023 |
| 5115 | ADMA Biologics Boca Raton, FL Chemist I B.S. in Chemistry, Biochemistry, Molecular Biology or related science discipline. Exp: 0-3 years |
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Chemist I! The Chemist I will Perform quality control testing of raw materials, in-process and final products; following general instructions on routine work and detailed instructions on new assignments. | 3/9/2023 |
| 5116 | ADMA Biologics Boca Raton, FL QC Microbiologist I, Product Testing B.S. in Biological Science or related science discipline. Exp: 0-3 years |
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a QC Microbiologist, Product Testing. The QC Microbiologist, Product Testing will Perform quality control testing of raw materials, in-process samples and final products | 3/9/2023 |
| 5117 | ADMA Biologics Boca Raton, FL Raw Material Specialist I B.S. or associate degree in Chemistry, Biochemistry, Biology or related science discipline. Exp: 0-3 years |
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Raw Material Specialist I! The Raw Material Specialist I will perform quality control raw material processing and testing. Following general instructions on routine work and detailed instructions on new assignments. | 3/9/2023 |
| 5118 | Admera Health South Plainfield, NJ Associate Scientist I/II Bachelor’s degree in Biological Sciences or M.S. in Biological Sciences Exp: BS: 1-3 years; MS: 1 year |
Responsibilities: • Preparing solutions and reagents for performing assays on the bench. • Perform Next Generation Sequencing-based genomic assays on different workflows (few listed below): o RNAseq o Whole Genome Sequencing o Whole Exome Sequencing • Carry out genomic assays under Biosafety Level II Policies and in regulatory compliance. • Perform Operational Qualification and Performance Qualification on Next Generation Sequencers. • Strictly follow standard operating procedures set forth for processing biological specimens while complying with laboratory safety protocols. • Strict recordkeeping of all laboratory procedures. • Continue acquiring next generation sequencing knowledge to support molecular biology techniques. • Collaborate within the group and cross departmental to achieve goals. | 3/9/2023 |
| 5119 | Patheon St Louis, MO QC Scientist I (Bioassay) Bachelor’s Degree in a Biological Science or related field Exp: 1 year |
The QC Analytical Scientist’s primary responsibility is to perform routine to sophisticated QC testing pertaining ELISA testing and Cell Based Assays in accordance with cGMP regulations and Thermo Fisher standards to meet departmental and interpersonal goals. This position entails testing for GMP release and stability along with support for the validation and qualification of ELISA and Cell Based Assays. Additional responsibilities include supporting the department to establish robust work processes and assess for continuous improvement opportunities. The QC Analytical Scientist will report directly to the QC Analytical Bioassay Supervisor. | 2/28/2023 |
| 5120 | Patheon San Francisco, CA Cell Therapy Specialist Bachelor’s or Associates degree in a technical field desired. Exp: 1+ years |
Thermo Fisher Scientific is making a significant investment in the dynamic and rapidly growing Cell Therapy space. Our Cell Therapy organization within the Pharma Services Group, is one of the fastest growing areas of Thermo Fisher Scientific. We focus on providing development and clinical scale services for gene and non-gene modified cell processing for a variety of unmet medical needs. | 2/28/2023 |
| 5121 | Patheon San Francisco, CA Scientist I, Process Sciences BS or MS in biological science or engineering field preferred Exp: BS: 1+ years; MS: 0-1 years |
The Scientist I, with mentorship, will apply technical skills to conduct experiments and studies to support our clients cell therapy needs and to assist in meeting the goals of the Cell Therapy group. These functions may include but are not limited to activities such as cell isolation and separation, genetic modification (vector transduction and genomic editing), expansion methods (small, intermediate, and large scale), cryopreservation, technology transfer and design of technical documents. | 2/28/2023 |
| 5122 | Patheon Florence, SC Analytical R&D Scientist I Bachelor’s degree in chemistry or related field required. Exp: 1-2 years |
The Scientist I conducts laboratory work as necessary to assure that products are tested per operating procedures. Ensure that work is carried out in an efficient and safe manner. Utilizes judgment in making adaptation and modifications on all assignments. Provides routine analyses in an analytical chemistry laboratory following standard practices. Performs analytical methods as assigned for testing on raw materials, samples, stability, production intermediates, and active pharmaceutical ingredients, including method development and qualification activities. Supports internal development and/or manufacturing operations. Makes detailed observations and reviews, documents, and communicates test results | 2/28/2023 |
| 5123 | Patheon Cranbury, NJ Research Scientist I Bachelor of Science (B.S.) in chemistry or related field Exp: 1+ years |
The Research Scientist I role is responsible for helping to develop recombinant cytokine products for the life-science research market. This role will report to our Director, Lab Operations. Day-shift Opportunity | 2/28/2023 |
| 5124 | Patheon Frederick, MD Scientist I, Formulation Bachelor’s degree in scientific field required. Exp: 1-3 years |
The Advanced Cell Systems Production team at Thermo Fisher Scientific is responsible for manufacturing various Primary tissue derived products including cells, RNA and subcellular fractions along with reagents and for a variety of biological applications. Our team is dynamic and fast paced, relying on teamwork, multitasking and communication within the team and the larger organization. We are seeking an energetic individual with strong communication, technical and operational skills to join our team. The candidate will follow SOPs and work in compliance with EH&S, GLP, and any other required manufacturing or company systems (e.g. E1, Agile, Trackwise, etc.). This position will be responsible for supporting the team in achieving daily production schedules and product quality goals. | 2/28/2023 |
| 5125 | PCI Pharma Services Bedford, NH QC Chemist I (Wed - Sat 6:30 AM - 5:00 PM) Bachelor of Science in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study Exp: 0-3 years |
This position will have responsibility to support various activities in the Quality Control Laboratory. This includes testing the following sample types R&D, in-process, finished product, stability, as well as raw materials. Job duties may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management | 2/28/2023 |
| 5126 | PCI Pharma Services Philadelphia, PA Process Engineer Bachelor's Degree in Mechanical or Packaging Engineering or related field Exp: 1-5 years |
The Process Engineer is responsible for identifying and mitigating packaging issues for existing business through strong engineering and process improvement methods. Provide technical leadership for new product launches. Lead continuous improvement activities. Secondary tasks include specify, purchase, and commission new equipment and manage capital finances. Provide technical support for new business (Sales/Business Development Support). All activities are focused around technical and operational support to the production, maintenance, and support staffs in the areas of process improvement, equipment modification and optimization, safety, and quality improvement, and increasing throughput. This is achieved through individual effort and facilitation of teams, tracking and analysis metrics, strong understanding and utilization of good engineering practices, project management, and the use of Lean Six Sigma techniques. Additionally, the Process Engineer will be responsible determining staffing, equipment needed, equipment purchase, equipment installation, component layout and line layout. | 2/28/2023 |
| 5127 | PCI Pharma Services Bedford, NH QC Chemist I Bachelor of Science in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study Exp: 0-3 years |
This position will have responsibility to support various activities in the Quality Control Laboratory. This includes testing the following sample types R&D, in-process, finished product, stability, as well as raw materials. Job duties may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management. | 2/28/2023 |
| 5128 | PCI Pharma Services Rockford, IL Laboratory QA Specialist 1 Bachelor's Degree in a related field Exp: 1-5 years |
The primary function of the Laboratory QA Specialist I is the timely and efficient review ensuring accuracy, completeness and compliance to in–house, customer and regulatory requirement, including data integrity, are met following the testing of pharmaceutical starting materials, components and finished products using techniques such as manual/automated titrations, UV, FTIR, LOD, Karl Fisher, Water activity and Pharmacopoeial testing i.e. LOD, RI, ID, Limit tests, Training of personnel in data review in area of expertise. Author OOS investigations, determination of root cause and develop and implementation of corrective and preventative actions. Author investigations into deviations from defined procedures. Review of regulatory bodies for changes applicable to the laboratory and ensuring that any changes are implemented. Maintain metrics with respect to area of responsibility. | 2/28/2023 |
| 5129 | PCI Pharma Services San Diego, CA Engineer, Sterile Fill & Finish Bachelor's Degree in a related field Exp: 1-3 years |
This role is responsible for engineering and technical oversight of the equipment and facilities of the Sterile Fill & Finish (SFF) implementation project(s) in San Diego. This person will become the technical Subject Matter Expert (SME) for the Cytiva isolator filling technology implemented in San Diego as well as the associated processing equipment related to formulation and sterile filling. This position will define relevant operational/technical standards and practices for the San Diego SFF operation and identify and drive the implementation of improvements to maximize throughput and capacity utilization. The role will interface with other PCI functions as well as external clients to implement new sterile filling projects and technologies into PCI GMP manufacturing. Responsible for the generation and execution of validation protocols, assistance in audits, determination of validation needs, and training of SFF staff. | 2/28/2023 |
| 5130 | Complete Genomics San Jose, CA Research Associate, Reagent Development Bachelor’s degree or Master's degree in Molecular and Cellular Biology, Chemistry, Biochemistry, or related field. Exp: 1-3 years |
This position is for a self-motivated and detail-oriented Research Associate with hands-on wet-lab experience to support our NGS service and lab. The candidate should be able to execute experiments independently, communicate with team players effectively, and interpret and document results in a timely fashion. | 2/28/2023 |
| 5131 | Poseida Therapeutics San Diego, CA Quality Control Analyst Bachelor’s or Master’s degree in life sciences or a related field Exp: 0-1 years |
Poseida is seeking an outstanding candidate to join our Quality team. The Quality Control Analyst is a member of a dynamic team that ensures the safety of our products at various points during the manufacturing process and confirms they meet predefined criteria. Working cross-functionally and collaborating with individuals and functions both within Poseida and at third parties, they will support the Quality department goals, participate in and promote Quality culture. | 2/28/2023 |
| 5132 | ProMed Molding Plymouth, MN Analytical Scientist Bachelor’s degree Exp: 0-3 years |
The Analytical Scientist performs a wide variety of analytical test method development, method validation, and routine testing activities for formulation and product releases. Including quality control related to testing of incoming materials, commercial, research and development pharmaceutical dosage forms and medical device combination products to support formulation and product release activities. The Analytical Scientist ensures ProMed’s brand, philosophy, systems, policies, and procedures are properly implemented and observed. | 2/28/2023 |
| 5133 | Prominex San Diego, CA Research Associate I/II Master’s degree in Science Exp: 0-2 years |
Prominex Inc. is a startup molecular diagnostic company with an experienced team of passionate and energetic scientists driven to create fast and affordable molecular diagnostic solutions across the globe. We are focused on infectious disease assays in point-of-care and home-based settings. We are looking for an enthusiastic and dedicated Research Associate to implement and execute analytical and scientific experiments to drive Product Development. Demonstrates high degree of organization and planning and the ability to apply scientific principles to plan out and execute experiments involving a variety of laboratory methods. This individual demonstrates technical proficiency, high degree of organization and planning and the ability to apply scientific principles. | 3/1/2023 |
| 5134 | Resilience Alachua, FL Specialist, Biomanufacturing B.S. (Biology, Microbiology, Chemistry or equivalent) Exp: 0-2 years |
This position will assist in production related activities in the cGMP Manufacturing Core according to established procedures at the Medical Counter Measures (MCMs) Advanced Development and Manufacturing Facility in Alachua (Florida). | 3/1/2023 |
| 5135 | Rocket Pharmaceuticals Cranbury, NJ Entry Level - Clinical Manufacturing Associate I - Upstream B.A./B.S. in Life Science, Biotechnology, ChemE, or similar relevant field Exp: 0 to 2 years’ |
As a Clinical Manufacturing Associate I, you will be part of a team responsible for the start-up of a cleanroom facility and the cGMP manufacture of viral vector therapies for use in clinical trials. Additional responsibilities include set-up, operation, and cleaning of equipment, equipment, and process monitoring and troubleshooting, receiving materials and supplies from the warehouse, maintaining supply inventories, creating technical documents, and maintaining cleanrooms and equipment in an inspection-ready state. The ideal candidate will also have a strong passion and curiosity for science and gene therapy with the desire to contribute individually and collectively in a dynamic, fast-paced environment. | 3/1/2023 |
| 5136 | Rocket Pharmaceuticals Cranbury, NJ Associate Scientist, Quality Control BS in Biology, molecular biology, virology, Life Sciences or equivalent Exp: 0 - 2 years |
We are seeking an Associate Scientist, Quality Control with the responsibility to support clinical manufacturing of a range of Gene Therapy products. Technical proficiency in analytical methodology for drug substances and drug products is required for gene-based products. | 3/2/2023 |
| 5137 | Tectonic Therapeutic Watertown, MA Research Associate/Senior Research Associate – Protein Sciences (Protein Biophysics) Bachelor’s or Master’s degree in analytical or biophysical chemistry or related discipline Exp: 1-3 Years |
The (Senior) Research Associate for Tectonic will be a highly collaborative team player who has experience characterizing proteins using a wide array of analytical and biophysical techniques. Hands-on experience with standard biophysical techniques is required and experience with assay development is a plus. The successful candidate will contribute to our core research capabilities and the development of our anti-GPCR antibody discovery platform. The candidate would conduct established biophysical assays and perform continuous development and improvement over time. This position represents a unique opportunity for the successful applicant to join an innovative start-up at the heart of the Boston biotech ecosystem and to contribute to its long-term Success. | 3/3/2023 |
| 5138 | Tevard Biosciences Cambridge, MA Research Associate, in vivo pharmacology BS/MS in Neuroscience, Physiology, Molecular/Cellular Biology, or a related Life Science discipline Exp: 0-2 years’ |
We are looking for Research Associate (RA-I or RA-II) with an innovative mindset, great attention to detail and ability to work collaboratively to solve problems, to help advance therapeutic candidates to the clinic. The successful candidate will have an opportunity to positively impact patients with serious unmet medical needs while working closely with our world-class scientific team, including with company’s scientific co-founders. In this position, you will collaborate with the in vivo pharmacology team to study effects of therapeutic lead candidates. The RA will work with animal models for rare genetic diseases and will be responsible for executing experiments to quantify molecular, cellular, and physiological readouts, in addition to supporting in vivo dosing studies and related research activities within the in vivo pharmacology group. This is an exciting opportunity for a motivated scientist to further develop their skills in neuroscience, physiology and gene therapy while helping to make an impact on lives of patients suffering from rare diseases. | 3/3/2023 |
| 5139 | Thrive Earlier Detection Cambridge, MA Research Associate I - Molecular Biology (Temporary) Bachelor’s degree in Life Sciences, Medical Technology, Clinical Laboratory Science, Chemical/Physical/Biological Science, or related field. Exp: 1+ years |
The Research Associate I, with guidance from more experienced scientists, assists in the day to day experimental work that includes execution of bench experiments, and gathering and assembling of data. Working in a team setting, the Research Associate I will primarily be involved in Research and Development projects assisting in translating research ideas and concepts into the product development pipeline towards development of diagnostic assay products. | 3/3/2023 |
| 5140 | Amniox Medical Miami, FL R&D Validation Engineer Bachelor of Science in Engineering (preferred), Biology, Chemistry, Biochemistry, or other technical discipline is required. Exp: 1 year |
The incumbent will be responsible performing basic to moderate level engineering tasks to support the development of new and existing HCT/Ps, medical devices, cosmetics, and biologics as well as to support compliance of the Research and Development laboratory to FDA and ISO standards. Primary responsibilities will include coordinating and supporting activities for product development; to include design verifications, process validations, and stability studies; as well as to support the validation/qualification of laboratory computer systems (including analysis spreadsheets, instrument software systems, laboratory information management system (LIMS), electronic laboratory notebook (ELN) systems, inventory management, and other specialized software). Additional responsibilities include supporting the manufacturing of developmental products in a Good Manufacturing Practice (GMP) facility and to support clinical and laboratory tasks and other duties for the Product Development department following Good Clinical Practice (GCP) and Good Laboratory Practice (GLP), where applicable. | 3/3/2023 |
| 5141 | Amniox Medical Miami, FL Associate I, Manufacturing P/T & F/T Bachelors or associates in biological sciences, or a related field preferred. Exp: 1-3 years |
The incumbent will be responsible processing human birth tissue in an FDA regulated environment and following all cGMP requirements. | 3/3/2023 |
| 5142 | Toxicon Somerset, NJ Research Analyst I - BioAnalytics Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1-3 years |
Labcorp Drug Development is the leading global Clinical Research Organization. We have an exciting career opportunity for an Research Analyst on our BioAnalytical team in Somerset, NJ. Are you interested in working in the research field? MUST have LCMS experience! The Analyst is focused on the extraction of biological samples (Protein Preciptation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. This position is a day shift with a flexible start time between 6am and 9am. Labcorp Drug Development is the leading global Clinical Research Organization. We have an exciting career opportunity for an Research Analyst on our BioAnalytical team in Somerset, NJ. Are you interested in working in the research field? MUST have LCMS experience! The Analyst is focused on the extraction of biological samples (Protein Preciptation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. This position is a day shift with a flexible start time between 6am and 9am. | 3/3/2023 |
| 5143 | Toxicon Bedford, MA Research Assistant · B.S. with a Biology background Exp: 1-3 years |
We are currently seeking a highly motivated, quality and detail oriented individual to join our In-Vitro Genetox team. The successful candidate will work closely with our study directors and quality assurance to ensure all study aspects are conducted per scientific and regulatory standards. This position is an integral component of a fast-paced environment. You will be joining a rapidly growing team and will be selected based on both experience/aptitude and a dynamic personality. The work is focused on in-vitro testing of medical devices and pharmaceutical products using Good Laboratory Practices (GLP). The main assays performed are AMES, MLA and Chromosomal Aberration testing. Studies are conducted under OECD and ISO guidelines, protocols, and Standard Operating Procedures.We are currently seeking a highly motivated, quality and detail oriented individual to join our In-Vitro Genetox team. The successful candidate will work closely with our study directors and quality assurance to ensure all study aspects are conducted per scientific and regulatory standards. This position is an integral component of a fast-paced environment. You will be joining a rapidly growing team and will be selected based on both experience/aptitude and a dynamic personality. The work is focused on in-vitro testing of medical devices and pharmaceutical products using Good Laboratory Practices (GLP). The main assays performed are AMES, MLA and Chromosomal Aberration testing. Studies are conducted under OECD and ISO guidelines, protocols, and Standard Operating Procedures. | 3/3/2023 |
| 5144 | Toxicon Somerset, NJ Veterinary Technician- Research Bachelor degree in Life Sciences, Associate degree in Laboratory Animal Technology or Veterinary Technology highly preferred. Exp: BS: No experience |
Explore research careers and be a part of something bigger as a Vet Technician-Animal Operations in Somerset, NJ. Do you have animal experience and a love for Science and Research? Labcorp Drug Development helps to develop new drugs, medical devices and diagnostics. Your role is vital to improving the health of family, friends and animals. Be a Part of the Bigger Picture of bringing medical advances to the forefront as quickly as possible!! Starting at $23.00 per hour with Career Growth potential as you master skills! $4,000.00 Sign On Bonus for New Hires! Explore research careers and be a part of something bigger! | 3/3/2023 |
| 5145 | Toxicon Somerset, NJ Habituation Study Technician Bachelor degree in Life Sciences Exp: BS: No experience |
Explore research careers and be a part of something bigger as a Study Technician-Animal Operations in Somerset, NJ. Do you have animal experience and a love for Science and Research? Labcorp Drug Development helps to develop new drugs, medical devices and diagnostics. Your role is vital to improving the health of family, friends and animals. Be a Part of the Bigger Picture of bringing medical advances to the forefront as quickly as possible!! Join the Somerset, New Jersey Team as a Habituation Study Technician! Implementation of animal habituation programs using positive reinforcement training and behavior scoring. | 3/3/2023 |
| 5146 | Toxicon Madison; Somerset; Greenfield, WI Study Technician- Anatomical Pathology Bachelor’s Degree in Life Sciences, or Associate Degree in Life Sciences, Histology, Laboratory Animal Technology or Veterinary Technology Exp: Graduating Seniors |
We have an exciting opportunity for December 2022 or May 2023 grads to join our Anatomical Pathology team in Madison, WI, Greenfield, IN or Somerset, NJ! Company Overview: At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions—because we know that knowledge has the potential to make life better for all. Here, you can apply your scientific curiosity in Biology, Animal Science, Zoology, Animal Behavior, Veterinary Technology, Dairy Science, Equine Science or similar majors to pursue advances in animal welfare and research the effectiveness, safety and toxicity of drugs in early development animal research studies. Your work will help medical, biotech, and pharmaceutical companies create life-saving vaccines and medicines that make a real impact on people’s lives. | 3/3/2023 |
| 5147 | Toxicon Bedford, MA Research Assistant - Chemistry Lab Operations Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1-3 years |
Explore research careers and be a part of something bigger as a Research Assistant for the Analytical Lab Operations in Bedford, MA! Labcorp Drug Development helps to develop new drugs, medical devices and diagnostics. Your role is vital to improving the health of family, friends and animals. As a Research Assistant I you will be responsible for providing technical expertise in supporting preclinical studies conducted under GLP, ISO 17025, and various other regulatory agencies. Research Assistants must work closely with study directors, analytical services staff, and quality assurance to ensure all study aspects are conducted in per scientific and regulatory requirements. Excellent communication skills needed as this position works closely with other research associates and scientists. Individual must be highly organized to handle multiple projects on an ongoing basis. | 3/3/2023 |
| 5148 | Trevigen San Marcos, CA Quality Control Specialist Bachelor’s degree in Biological Science, Chemistry, or related field. Exp: 1- 5 years’ |
Responsible for performing QC testing for Value Assignment assays, QC release assays, stability, physical/visual inspections, any related QC function. Assists in the flow of product in the QC department. | 3/3/2023 |
| 5149 | Trevigen Minneapolis, MN Research Associate, Microbiology QC Bachelor’s degree in Microbiology or a related scientific field or equivalent Exp: up to 3 years |
The responsibilities of this position are to participate in the Microbiology QC testing and reporting procedures: set up, read, and report the microbial QC bioburden and sterility testing of various sample types using culture methods that include direct plating, broth inoculation, and membrane filtration. Performance of environmental monitoring for viable microbes, particle counts, and WFI/deionized water testing, reading, and reporting. Assist with efficacy and validation testing, new procedure development, new equipment IQ/OQ and calibrations. Perform general lab duties, assist with sanitization of clean rooms, and additional duties as assigned. | 3/3/2023 |
| 5150 | Trevigen Minneapolis, MN Advanced Research Associate, Analytical QC Master’s degree in Biochemistry, Chemistry, Biology, or a related field Exp: 0 – 2 years |
The Advanced Research Associate, Analytical QC position will perform routine quality control testing of protein, peptide or antibody products using standard operating procedures to determine lot status, product release and product stability. Tests include: concentration determination, SDS-PAGE with densitometry, endotoxin assay, TOC, conductivity, pH, and other testing as assigned. Participation in the validation of new and existing laboratory methods is also expected. The position requires routine documentation, analysis, and communication of results within the department and across different groups. Other duties include instrument calibration and maintenance, record keeping, and lab support. Within this job function, the Research Associate must also pursue annual goals that aim to facilitate innovation, efficiency, productivity, and team building across the QC Department or the entire company. Perform additional duties as assigned. | 3/3/2023 |
| 5151 | Trevigen Minneapolis, MN Research Associate, QC Bioassay Bachelor’s degree in the biological sciences or equivalent Exp: 0 to 2 years |
Perform routine QC testing of antibodies and proteins using standard operating procedures (SOP) to determine the status of the product. Conduct stability testing on proteins and antibodies to predict shelf life. Perform a variety of tests including: Direct ELISA, Functional ELISA, Western Blot, Array, ELISpot experiments, and Impurity ELISA (mycoplasma, host cell protein, host cell DNA). Participate in investigations, internal requests, and custom projects. Actively take part in group projects as needed. Assist with improving lab protocols. Perform additional duties as assigned. | 3/3/2023 |
| 5152 | Triangle Insights Group Durham, NC Life Science Research Associate Bachelor’s degree in relevant field Exp: 0-3 years |
The Research Associate role is an entry-level position on a small team supporting the strategic recommendations Triangle Insights Group, a strategy consulting firm, provides to its diverse portfolio of clients in the life sciences industry. The focus of this position is to collect and analyze data from secondary sources, as needed by consulting teams, in the pursuit of answering the complex business problems facing clients. The perfect candidate has a strong track record of academic achievement and an interest in the life science and pharmaceutical industries. | 3/3/2023 |
| 5153 | Triclinic Labs Lafayette, IN Analytical Scientist BS in chemistry or related field. Exp: 1-3 years |
Job Description: Triclinic Labs is seeking a scientist to: • Carry out instrumental analyses. • Aid in maintenance and repair of analytical instruments. • Process analytical data for inclusion in reports. • Participate in instrument software validation as necessary. • Be involved in multiple projects concurrently and exhibit flexibility to meet changing priorities. • Provide high-quality work output and accurate record keeping • Comply with all regulatory and laboratory requirements and policies. | 3/3/2023 |
| 5154 | Universal Cells Seattle, WA Research Associate II, Clinical Gene Editing in Seattle, Washington An MS Exp: 0-2 years |
The primary purpose of the Research Associate II for Clinical Gene Editing is to support the generation of clinical-grade, gene-edited Universal Donor Cells in a controlled manufacturing environment. This Research Associate II role will work as part of a team planning and executing all aspects of gene-editing and engineering of pluripotent stem cells. Will assist with complex laboratory operations, keep appropriate documentation including lab notebooks, batch documentation and experimental summaries. Will be able to execute protocols with minimal guidance and will have the ability to summarize results independently. May assist in generating content and preparing controlled documents and data summaries. This position will acquire further versatility in routine procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. | 3/3/2023 |
| 5155 | Universal Cells Seattle, WA Research Associate II, Molecular Analytics in Seattle, Washington MS Degree Exp: 0-2 years |
We are seeking a highly capable, self-motivated Research Associate II for our Core Technologies Department. This individual will contribute to the molecular engineering for our gene edited Universal Donor Cells with activities focused on performing custom TaqMan based PCR assays. They will work as a key member on a fast-paced team to run molecular assays to characterize our proprietary Universal Donor Cells. | 3/3/2023 |
| 5156 | Universal Cells Westborough, MA Research Associate II, Analytical Development in Westborough, Massachusetts MS Degree Exp: 0-2 years |
The Research Associate will support assay development and qualification activities by performing cell culture and wet lab experiments, analyzing data, and drafting protocols, SOPs, and reports. This individual will be expected to execute protocols with some guidance and have the ability to summarize results independently. They will collaborate closely within the team and across functional groups to advance pipeline programs. | 3/3/2023 |
| 5157 | Universal Cells South San Francisco, CA Associate Engineer in South San Francisco, California BS in Chemical/Mechanical/Biological Engineering or Life Sciences; MS in Chemical/Mechanical/Biological Engineering or Life Sciences. Exp: BS: 1-3+ years; MS: 1-2+ years. |
As part of the Astellas Gene Therapy Center of Excellence (GTCOE) Engineering & Facilities enterprise team, the Associate Engineer will support day-to-day operations in our brand-new South San Francisco based Pilot Plant. The Pilot Plant affords a flexible, dynamic environment to execute small scale bioprocess operations for non-clinical material supply and to test innovative new processes and equipment to enable the next generation of manufacturing processes at Audentes. Responsibilities will include execution of test article production, engineering runs, and new process equipment evaluation. The role will include close collaboration with Process Development, Lab Management, Project Engineering, MSAT, and external vendors. This position is located in South San Francisco, CA. | 3/3/2023 |
| 5158 | Universal Cells South San Francisco, CA Pilot Plant Associate I in South San Francisco, California BS in Science or Engineering or equivalent experience Exp: Associate I: 1+ years |
Reporting to the Pilot Plant Manager, the Pilot Plant Associate will participate in upstream and downstream areas of AAV development in the Pilot Plant for new gene therapy programs and processes. This position will be located in South San Francisco, CA. | 3/3/2023 |
| 5159 | JGB BioPharma Consulting San Francisco Bay Area, CA Entry Level Organic Chemistry Contractor 2015 B.S. or M.S. in Organic Chemistry or Similar Exp: 1 year |
Join a mid-sized pharmaceutical company as they move their proven platform into a new therapeutic area Be involved in experimental design, applying findings to drive further research Organize results and present them in meetings with the broader team Continue to remain abreast on new developments in the field, apply this to your work in the lab Support overall laboratory efforts, including lab maintenance and supply preparation as needed. 2015 | 2/21/2023 |
| 5160 | Align Technology San Jose, CA Lab Technician Chemistry- Contractor Bachelor’s degree Exp: 0-2 years |
Align is looking for a Lab Technician Chemistry- Contractor for our San Jose California location. You will be responsible for supporting the new product development. The ideal candidate should have good understanding of working with chemicals and polymers. | 2/21/2023 |
| 5161 | Charles River Laboratories Cambridge, MA Research Study Technician I Associate degree (A.A./A.S.) in animal or laboratory science or related discipline. Bachelor's (B.A./B.S.) Degree preferred. Exp: six to twelve (6-12) months |
We are seeking a Research Study Technician 1 for our Insourcing Solutions Department located in Cambridge, MA. Observe, monitor, and document the health and physical environment within the Charles River Accelerator & Development Labs (CRADL) animal facility. Conduct in vivo experiments in rodents for multiple clients to support research programs. Collaborate with the veterinary staff to ensure that the health and welfare of laboratory animals are maintained in compliance with local, state, federal and institutional guidelines, and regulations. | 2/21/2023 |
| 5162 | Charles River Laboratories Cambridge, MA Research Study Technician I Associate degree (A.A./A.S.) in animal or laboratory science or related discipline. Bachelor's (B.A./B.S.) Degree preferred. Exp: six to twelve (6-12) months |
We are seeking a Research Study Technician 1 for our Insourcing Solutions Department located in Cambridge, MA. Observe, monitor, and document the health and physical environment within the Charles River Accelerator & Development Labs (CRADL) animal facility. Conduct in vivo experiments in rodents for multiple clients to support research programs. Collaborate with the veterinary staff to ensure that the health and welfare of laboratory animals are maintained in compliance with local, state, federal and institutional guidelines, and regulations. | 2/21/2023 |
| 5163 | Charles River Laboratories Cambridge, MA Research Study Technician I Associate degree (A.A./A.S.) in animal or laboratory science or related discipline. Bachelor's (B.A./B.S.) Degree preferred. Exp: six to twelve (6-12) months |
We are seeking a Research Study Technician 1 for our Insourcing Solutions Department located in Cambridge, MA. Observe, monitor, and document the health and physical environment within the Charles River Accelerator & Development Labs (CRADL) animal facility. Conduct in vivo experiments in rodents for multiple clients to support research programs. Collaborate with the veterinary staff to ensure that the health and welfare of laboratory animals are maintained in compliance with local, state, federal and institutional guidelines, and regulations. | 2/21/2023 |
| 5164 | Charles River Laboratories Boston, MA Research Associate I Requires a BS in the biological sciences or relevant area Exp: 0-3 years |
Explora Biolabs a Charles River Company, is seeking a Research Associate to join its team in Boston, MA. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed in Essiential Duties and Responsibilities are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. | 2/21/2023 |
| 5165 | Charles River Laboratories S. San Francisco , CA Research Study Technician I Associate degree (A.A./A.S.) in animal or laboratory science or related discipline. Bachelor's (B.A./B.S.) Degree preferred. Exp: six to twelve (6-12) months |
We are seeking an experienced Research Study Technician I for our Insourcing Solutions site located in South San Francisco, CA. | 2/21/2023 |
| 5166 | Charles River Laboratories S. San Francisco , CA Research Study Technician I Associate degree (A.A./A.S.) in animal or laboratory science or related discipline. Bachelor's (B.A./B.S.) Degree preferred. Exp: six to twelve (6-12) months |
We are seeking an experienced Research Study Technician I for our Insourcing Solutions site located in South San Francisco, CA. | 2/21/2023 |
| 5167 | Charles River Laboratories Worcester, MA Research Technician I High school diploma or General Equivalent Degree (G.E.D.). Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: |
We have an exciting opportunity for a Research Technician 1 at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. We have an exciting opportunity for a Research Technician 1 at our Discovery site located in Worcester, MA. | 2/21/2023 |
| 5168 | Leica Biosystems Fargo, ND Process Validation Engineer I B.A. or B.S. in Biology, Biochemistry, Engineering or related science Exp: 0-3 years' |
The role of the Engineer I- Process Validation will be to support internal and external Cleaning Validation activities with projects focused on understanding and optimizing cleaning processes to improve product quality, cost, and process efficiency. Additional responsibilities include supporting Process Validation and Facility Environmental Monitoring Qualifications to ensure the production environment is compliant with regulatory requirements. This role has a large focus on documentation generation and some lab work both within the GMP manufacturing space and R&D environment. | 2/21/2023 |
| 5169 | Leica Biosystems Logan, UT Manufacturing Engineer Bachelor's Degree in a related engineering/technical degree Exp: 1 – 6 years |
Actively engage and support engineering priorities in response to manufacturing and plant priorities related to safety, quality, production, and cost/efficiency. Develop, lead or participate in various process improvement projects. Drive continuous improvement (LEAN) initiatives through application of sound engineering/reliability program elements and a data driven approach. Design, install, validate, and qualify new equipment to address key gaps in manufacturing Ensure that engineering support is performed in compliance with cGMP Regulations and Company Policies/Procedures. | 2/21/2023 |
| 5170 | Leica Biosystems Vancouver, British Columbia, CA Research Associate - Product Development Bachelors or Masters degree in a relevant scientific discipline (e.g. chemistry, biochemistry, pharmaceutical sciences, nanotechnology, materials scie Exp: 1 year |
Precision NanoSystems has an opening for a Research Associate, Product Development to join our growing team in Vancouver, BC. The successful RA will become an expert in the formulation and characterization of nucleic acid lipid nanoparticles (LNPs). They will design and perform experiments to support a variety of new product development projects, contributing to the development of novel technologies such as GenVoy-ILM delivery reagents for genetic medicine applications. The successful candidate will have a diverse set of laboratory skills and be technically excellent, with attention to detail and a track record of successful research contributions. | 2/22/2023 |
| 5171 | Leica Biosystems Ashland, VA Analytical Laboratory Technician-Coupons Associates or Bachelor’s Degree in Chemistry or related science degree Exp: 0-2 years’ |
The Analytical Lab Technician performs defined analytical procedures on various samples under the guidance of senior associates, provides basic support, inventory management and upkeep of equipment | 2/22/2023 |
| 5172 | IQVIA Indianapolis, IN Associate Scientist, Biotransformation Bachelor's Degree in chemistry, biochemistry, biology or related field required. Exp: 1 year |
Analyze and report in vitro and in vivo biotransformation studies, with focus on analytical method development, metabolite profiling, and reporting. Collaborate with senior staff regarding study execution as it relates to timelines, data quality, and interpretation of results. | 2/22/2023 |
| 5173 | MEDTOX South San Francisco, CA Lab Technician - Entry level, will train! BS/BA degree in Biology, Chemistry, or similar biological scientific discipline Exp: Entry-Level |
This is a great entry-level opportunity to join an innovative laboratory and receive targeted one-on-one training that will help the individual grow in a career in the biotechnology field! The schedule for this position will be Monday – Friday, 6am-2:30pm, with rotating weekends (one month on, one month off working weekends).This is a great entry-level opportunity to join an innovative laboratory and receive targeted one-on-one training that will help the individual grow in a career in the biotechnology field | 2/22/2023 |
| 5174 | PerkinElmer San Diego, CA Research Associate - Bioassay Bachelor’s Degree in Science (Biology, Immunology, or other related discipline) Exp: 0-2 years |
This position will contribute to the release of new GMP products by performing bioassay to test recombinant proteins and neutralizing antibodies. The main responsibilities include performing bioassay testing, troubleshooting bioassay, preparing documents following good documentation practice. Additional responsibilities include culturing mammalian cell lines, isolating primary cells, and maintaining laboratory equipment and supplies. The position requires careful documentation skills. | 2/22/2023 |
| 5175 | PerkinElmer San Diego, CA Biochemist I - Recombinant Purification Bachelor of Science in biological sciences Exp: 1 year or more |
This position is responsible for manufacturing cutting-edge recombinant protein research products in the Recombinant Manufacturing group. The biochemist will be involved in different stages of production of various recombinant protein products, with a focus on recombinant protein purification. Another part of the job responsibility includes preparing product/project-related documentation, and maintaining the record for recombinant protein products. | 2/22/2023 |
| 5176 | PerkinElmer Lafayette, CO Scientist 1 Bachelor’s Degree in Biology or similar life sciences degree Exp: 1-3 years |
Horizon has an exciting opportunity for an enthusiastic Scientist I for molecular biology/viral production. The Scientist I position will perform primary tasks in an ISO 9001:2015 biology manufacturing laboratory in Lafayette, CO. Key responsibilities for this position include a wide array of duties related to the processing and preparation RNAi and Gene Editing products including molecular biology bench work, cloning, viral production, nucleic acid purification, collection replication, inventory control, and order packaging. The position will require the ability to learn and to troubleshoot various aspects of molecular biology including cloning and mammalian tissue culture. | 2/22/2023 |
| 5177 | PerkinElmer San Diego, CA Research Associate - Antibody Development Bachelor of Science or equivalent degree with a course works in cell biology, immunology, and biochemistry Exp: 1+ years |
This position is responsible for producing monoclonal antibodies derived from various materials such as hybridoma cultures. Basic tissue culture and/or purification responsibilities include performing cell culture work, antibody purification and associated quality control steps including purity analysis, isotype testing, mycoplasma detection, Ig quantitation, and specificity measurement by assigned methods. Detailed performance documentation, database entry and report preparation are also required. In addition, efforts for technical troubleshooting, inventory and laboratory maintenance will be expected to support team. | 2/22/2023 |
| 5178 | PerkinElmer San Diego, CA Quality Control Associate I (PM Shift) Bachelor’s Degree in Science with previous experience in a laboratory setting Exp: 1+ year |
QC Flow Associates focused on cell & tissue culture are highly motivated team members that will primarily be responsible for the preparation of primary cells and the culture of various cell lines, as well as the set up of cell stimulations needed for flow cytometry testing of BioLegend products such as antibodies, protein reagents, buffers for immunology and related research fields. In addition, the employee may perform surface, intracellular, and multicolor testing and analysis. Primary responsibilities include performing experiments (e.g. cell culture, cell preparation and flow cytometry testing); production and analysis of reliable, reportable data; maintaining accurate documentation, utilization of internal company databases for product filing and retrieval; following company SOPs and ISO requirements. | 2/22/2023 |
| 5179 | PerkinElmer San Diego, CA Biochemist I - Custom Solutions PURE Bachelor’s degree in Biochemistry, Chemistry, or other related area Exp: 1 year |
BioLegend has an opening for a self-motivated individual with manufacturing experience in a fast moving and dynamic environment to join our Custom Solutions Team! The Biochemist I will be an integral member of a team, that manufactures and provides purified antibodies to enable studies for novel applications in precision medicine, oncology, immunology, neuroscience, and stem cell research. This position will report to a team lead and will ensure the highest quality of our finalized antibody products. This is a great opportunity to work in a fast-paced and dynamic environment for you to enhance your knowledge in the biotechnology industry! In this position you will manufacture custom purified antibodies under ISO13485 standards, troubleshoot problematic errors, continue to improve methodologies for efficiency, follow Standard Operating Procedures (SOP)s, and cross train on a variety of other supporting tasks. | 2/22/2023 |
| 5180 | Sanofi Framingham, MA QC Microbiology Analyst 1 (Wed-Sat 2nd shift) Bachelor’s Degree Exp: 0-2 Years |
This position is responsible for performing routine and complex testing of in-process samples and final products in accordance with SOPs and relevant procedures for method development, qualification, validation, method transfer, product release, stability, and process validation and investigations. | 2/22/2023 |
| 5181 | Invitrogen South San Francisco, CA Associate Scientist - Organic Chemistry Bachelor's degree or master's degree in Chemistry, Process Chemistry, or Organic Chemistry. Preference to master’s degree. Exp: 1+ year |
As an Associate Scientist (Research Associate), you will use state-of-the-art technologies to perform high-quality research for key pharmaceutical clients across the industry. Your problem-solving skills are an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. You will join the Small Molecule team while working onsite at the client location to support various GMP/GLP campaigns. | 2/22/2023 |
| 5182 | Invitrogen Rockville, MD Associate Scientist - mRNA Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0-2 years |
To perform the following activities for Drug Product support. This list is not all-inclusive and is subject to the needs of the project, but they will be responsible for planning and executing experimental studies in the area of mRNA lipid nanoparticle production and process optimization. | 2/22/2023 |
| 5183 | Invitrogen Cranbury, NJ Research Scientist I Minimum Bachelor of Science (B.S.) in chemistry or related field Exp: 1+ years |
The Research Scientist I role is responsible for helping to develop recombinant cytokine products for the life-science research market. This role will report to our Director, Lab Operations. Day-shift Opportunity | 2/22/2023 |
| 5184 | Krystal Biotech Pittsburgh, PA Laboratory Specialist/Associate Bachelor’s degree (Information Technology, Life Sciences or Engineering) Exp: 1+ years |
Krystal Biotech, Inc is seeking a highly motivated Laboratory Specialist/Associate who will work under the direction of the Quality Systems Manager. This role will support the development of Laboratory & Quality Systems (LIMS, QMS, and DMS), as well as assisting lab personnel with troubleshooting and software issues. | 2/22/2023 |
| 5185 | Krystal Biotech Pittsburgh, PA QC Microbiologist (Cleanroom) Bachelor’s Degree (Biology or related Life Science) Exp: 1+ years |
Krystal Biotech, Inc is seeking a highly motivated Quality Control Microbiologist to drive and sustain a comprehensive Cleanroom Environmental Monitoring Program that ensures regulatory compliance and promotes a strong culture of environmental cleanliness. This role will support the growing EM Department in sample collection and laboratory analysis. | 2/23/2023 |
| 5186 | Krystal Biotech Pittsburgh, PA Research Associate, Analytical Sciences and Clinical Testing Services Minimum of a Bachelor’s degree (Biology, Biochemistry, Chemistry, or related science) Exp: 0-2+ years |
Krystal Biotech, Inc is seeking a highly motivated a Research Associate, Analytical Sciences and Clinical Testing Services to perform high quality analytical testing in support of Krystal’s process development and product development efforts. This position will be laboratory based. | 2/23/2023 |
| 5187 | LakePharma Lebanon, NJ Analytical Chemist I- (Quality Control) Bachelor’s degree in Chemistry or related field Exp: 0-1 years’ |
The Analytical Chemist I I is responsible for performing routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished formulations, stability samples and for special projects, method development/transfers and cleaning study qualifications. | 2/23/2023 |
| 5188 | LakePharma Rensselaer, NY Research Scientist I; Medicinal Chemistry Bachelors or Masters Degree with major in chemistry Exp: 0-5 years |
The Research Scientist I is an integral part of the Curia team, contributing to our success by the synthesis, purification and identification of intermediates and target compounds. The Research Scientist I is expected to demonstrate expertise in both the theoretical and practical aspects of organic chemistry. Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients’ lives with the pharmaceuticals we develop and manufacture. | 2/23/2023 |
| 5189 | LakePharma Springfield, MO Quality Assurance Specialist I Bachelor’s degree in Life Science or related field Exp: 0-3 years’ |
Essential job duties • Maintain Quality databases including Archival and scanning of cGMP documents and records, Departures, media fill programs, and training files • Represent Curia Quality Assurance when managing issues that require immediate corrective action. Ensure such action taken is appropriate and correctly documented • Solicit feedback from various departments for operational improvement • Author, review, and/or approve Quality Management System documents, including, but not limited to, change controls, SOPs, deviations, CAPAs, etc. | 2/23/2023 |
| 5190 | LakePharma Hopkinton, MA Quality Control Lab Technician I AS required or BS preferred in life sciences including biology, immunology, biochemistry, process engineering or a similar biological science Exp: 0-3 years |
We are rapidly growing and seeking a talented individual to join our Quality Control Team as a QC Microbiology Technician. The role will report directly to the Supervisor of QC Microbiology and will be based in our Hopkinton, MA facility. The ideal candidate will support cGMP validation and routine release testing for raw materials, in-process, drug substance and finished product testing for products produced at the Hopkinton GMP manufacturing facility. | 2/23/2023 |
| 5191 | Larimar Therapeutics Bala Cynwyd, PA Associate Scientist/Scientist, Bioanalytical M.S. in Biology, Biochemistry, Chemistry, or related field Exp: 1 year’ |
Larimar Therapeutics is a clinical-stage biotechnology company focused on the treatment of mitochondrial related and other rare diseases. The company is recruiting a motivated Associate Scientist/Scientist, Bioanalytical. The incumbent will monitor bioanalytical activities at external partners in support of program development. This would be a good opportunity for people who would like to transit from bench work to project management. | 2/23/2023 |
| 5192 | Lygos Berkeley, CA Fermentation Process Engineer I-II B.S. in chemical engineering or related fields Exp: 1-2 years |
Lygos is seeking a process engineer candidate to maintain, set up, run, troubleshoot and clean pilot scale bioreactors. The successful candidates will have experience with instrumentation and hands-on experience working on pilot scale bioreactors. The candidate will report to the Director of Fermentation. | 2/23/2023 |
| 5193 | Lygos Berkeley, CA Fermentation Research Associate Bachelor’s degree in Chemical Engineering or a related field Exp: 0-3+ years |
Lygos is seeking a Fermentation Research Associate to maintain, set up, run and clean bench-top level bioreactors (0.25L-150L). The successful candidate will have experience with general lab procedures, sterile techniques, data interpreting/reporting and will be comfortable working in a fast paced, multitasking environment. This person will have ample opportunity to participate in other aspects of Lygos’ technical efforts, including media optimization, batch work in flasks and 96 well plates, downstream processing development, lab build-out and other aspects of technology development, deployment, and commercialization. The Lygos team works closely with all employees to support career development and facilitate the learning of new skills! | 2/23/2023 |
| 5194 | Mammoth Biosciences Brisbane, CA Research Associate II, CRISPR Platform (High-throughput Mammalian Screening) Bachelor’s degree in molecular and cell biology, immunology, biochemistry, or a related field Exp: 1+ year |
Mammoth is currently seeking a creative and detail-oriented Research Associate II with experience in molecular biology, next-generation sequencing, and/or mammalian cell culture to join our CRISPR Platform team. The successful candidate will work collaboratively with colleagues to develop and execute high-throughput experiments in mammalian cell lines to support the development of novel Cas nucleases for therapeutic genome editing. They will have the opportunity to contribute broadly across multiple technical areas, including automation, software tool development, synthetic biology, and high-throughput screening. This position requires adaptability, strong organizational and communication skills, and the ability to work both independently and collaboratively in a dynamic team-oriented environment. | 2/23/2023 |
| 5195 | Masy BioServices Wilmington, NC Associate Scientist I/II Bachelor’s degree in Chemistry or a related field. Exp: 0 – 4+ years |
The Associate Scientist I or II is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Associate Scientist may also assist with method development/method validation projects. For this position, HPLC, dissolution and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: CKF/KF, ICP-MS, Particle Size, CCIT, UV. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 2/23/2023 |
| 5196 | Masy BioServices Wilmington, NC Associate Scientist I/II Bachelor’s degree in Chemistry or related field Exp: 0 – 4+ years |
The Associate Scientist I or II is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of active pharmaceutical ingredients development or pharmaceutical manufacturing. This position may also be required to work on method development/method validation projects. Typical types of testing include: assays (potencies, related substances, residual solvents, metals etc.), moisture content, identification, and various other wet chemistry based measurements. HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations, UV, DSC, TGA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client/vendor supplied or developed by Alcami). The Associate Scientist II must have the ability to efficiently organize the routine work with minimum supervision and to properly evaluate and interpret generated data is required. The Associate Scientist II will occasionally be called upon to support and mentor other Analytical Chemists within the lab. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 2/23/2023 |
| 5197 | Med Institute West Lafayette, IN Chemist I Bachelor degree in Chemistry or Chemistry related field Exp: 0-2 years |
The Chemist 1 positions will perform release testing on raw materials and finished products using United States Pharmacopoeia (“USP”) compendial methods, client methods, and methods developed in house. Assist in the development and validation of analytical methods for drug products, placebo, and raw materials in the Cook Biotech Analytical Laboratory. | 2/23/2023 |
| 5198 | Meridian Life Science Memphis, TN Senior Research Associate Masters’ degree from an accredited institution in a relevant scientific discipline such as Biology, Chemistry, Biochemistry, Molecular Biology etc. Exp: 1+ years |
The Senior Research Associate will be responsible for conducting research and providing technical assistance, within our Technical Operations and Development department, to drive the improvement and growth of our immunological reagent offerings including recombinant proteins, native antigens, antibodies, blockers, and custom manufacturing. The position is responsible for conducting research and performing upstream bioprocessing, downstream bioprocessing, and analytical analysis of biomolecules. The candidate will assist with the optimization and scale up of processes, troubleshooting manufacturing issues, improving product quality, and reducing manufacturing costs. The candidate will be responsible for performing routine laboratory maintenance and lab management duties including maintaining sufficient supply of reagents, cleaning and disinfecting of laboratory equipment, cleaning lab area, environmental monitoring, and filling out proper paperwork. The candidate must be able to execute assigned procedures in a fast-paced and results-oriented environment satisfying quality standards in accordance with customer satisfaction, cost, schedule, and ISO13485 regulations. | 2/23/2023 |
| 5199 | Lonza Portsmouth, NH Quality Control Microbiology Analyst Nights BS, AA in Microbiology, Biochemistry or Related Science Exp: 0 yrs |
The QC Analyst will act as a team member of the Quality Control department to support production of in-process and final product drug lots for customers. Also being able to participate in quality testing for ongoing customer stability studies. The QC Microbiology Analyst should be able to provide on-time, high quality results to meet Manufacturing demands. *This position is a night shift role that reports to work Mon-Fri 10PM-6AM*Training will be conducted during the day shift for a few weeks. While working 3rd shift, the employee will receive a 20% shift differential. While working on any Saturday or Sunday, this employee will receive an additional 5% shift differential. | 02/15/23 |
| 5200 | DiabetOmics Hillsboro, OR Research Assistant/Associate in Product Development (2 positions available immediately) BA/BS in a relevant biological science Exp: 1-2 years |
Diabetomics R&D group is currently seeking a Research Assistant/Associate to join our established team. Essential Functions: Supports the Diagnostic Product Development team. This is a hands-on, bench-level laboratory position. Tasks will include, but are not limited to: assay feasibility, assay development, optimization, reagent formulation, verification and validation studies. | 2/13/2023 |
| 5201 | DxTerity Rancho Dominguez, CA Laboratory Technician/Scientist Molecular Biology, Lab Operations S. or M.S. in chemical, biological or clinical laboratory science, or medical technology from an accredited institution. Exp: 1-3 years |
Testing biological specimens in molecular biology laboratory environment, including high throughput workflows, analyzing the results, and preparing them for reporting. | 2/15/2023 |
| 5202 | Fluxergy Irvine, CA Process Engineer Engineering degree Exp: 0-2 Years |
As the process engineer at Fluxergy, you will be directly involved in the company’s production activities, as well as deeply involved with the company’s long-term strategy. You will be responsible for process ownership while working with a small but passionate team. This position requires a deep, in-depth knowledge of manufacturing processes, stability and process control. | 2/16/2023 |
| 5203 | Fluxergy Irvine, CA Industrial Engineer Undergraduate or Masters degree in Industrial Engineering Exp: 1-2 years |
As the Industrial Engineer at Fluxergy, you will be directly involved in the company’s Production activities, as well as deeply involved with the company’s long-term strategy. You will be responsible for process improvement, scale up and capacity planning while working with a small but passionate team. This position requires a deep, in-depth knowledge of lean manufacturing and six sigma methodologies. | 2/16/2023 |
| 5204 | Frontida BioPharm Vandalia, OH QC Analyst Bachelor’s degree in chemistry or related field Exp: 0 to 3 years’ |
The essential job function is to perform physical and chemical testing of intermediate and finished products according to written procedures. | 2/16/2023 |
| 5205 | Frontida BioPharm Vandalia, OH Raw Materials Chemist Bachelor or Master’s degree in Chemistry or related field Exp: Chemist I: 0-2 years’ |
The Raw Materials Chemist will report to the Manager of Raw Materials QC, and will perform chemical and physical testing on pharmaceutical raw materials (APIs, Excipients and Packaging components). | 2/16/2023 |
| 5206 | Frontier Medicines South San Francisco, CA Research Associate, Protein Sciences BS or MS in Biochemistry, Biological Sciences, or a related field Exp: 0-2 years |
We are seeking highly motivated research associates to join our group in South San Francisco, CA. This is an exciting opportunity for experienced and passionate associates or recent graduates to apply and expand their skills in protein sciences and contribute to the discovery of innovative therapies. The successful applicants will carry out experiments in protein expression, purification, and characterization to support biochemical assays and structure determination. Working closely with an experienced team of interdisciplinary scientists, the candidates will have regular opportunities to present findings to the Protein Sciences team. The ideal associates should have a strong desire to learn new techniques and incorporate new methodologies into their work, as well as be detail-oriented, self-motivated, well organized, and enjoy working and learning in a dynamic team environment. | 2/16/2023 |
| 5207 | Fujufilm Diosynth Research Triangle Park, NC Production Technician (Weigh & Dispense) BS/BA Exp: 1+ years |
Write and review standard operating procedures, buffer formulation records. Assist senior staff in implementing project safety and quality assurance programs in accordance with SOPs. Maintain the confidentiality of proprietary company information. Document and maintain activity records according to cGMP regulations and ensure junior team members are trained. Operate general production equipment such as Autoclaves, Analytical Scales, pH/conductivity meters, etc. Lead/Perform daily cleaning and sanitization of the weight and dispense area and manufacturing SAP transactions i.e. goods issue, goods receipt, goods transfer. Receipt & lot numbering of incoming materials. Issue of materials to process orders and cost centers. | 2/16/2023 |
| 5208 | Fujufilm Diosynth Thousand Oaks, CA Manufacturing Associate Bachelor of Science (B.Sc.) Exp: 0-3 years |
The Manufacturing Associate works as part of the manufacturing team to deliver high quality cell therapy materials during process transfers, routine production, and technology improvements. This position contributes to the successful delivery of released product in support of clinical trials and commercial production. | 2/16/2023 |
| 5209 | Fujufilm Diosynth Thousand Oaks, CA Associate Scientist, Process Sciences Master of Science (M.Sc.) Exp: 1+ years |
The Associate Scientist, Process Sciences, is a critical position responsible for development activities associated with cell therapy process development and design at Fujifilm Diosynth Biotechnologies, California (FDBC). This position provides hands-on support for all aspects of process development experimental design and execution, will be responsible for experimental process monitoring (data capturing), and process troubleshooting. This position will work closely with and/or under the direction of a Senior or Principal Process Development Scientist. | 2/16/2023 |
| 5210 | Fujufilm Diosynth College Station, TX Process Sciences - Engineer I Master’s Degree preferably in Chemistry, Biology, Life Sciences or related field Exp: 0-3 years |
The Engineer I functions within a team based organization to actively address complex cGMP manufacturing issues. The individual is responsible for analyzing process technologies in support of new project proposals and assist in the technical transfer into the manufacturing group. This individual must work in a collaborative manner coordinating the transfer of biological drug processes from process development (internal or client) groups in a CMO environment. | 2/16/2023 |
| 5211 | Fujufilm Diosynth College Station, TX Quality Control - Microbiology Analyst I Bachelor of Science or Associate of Science degree preferably in Biochemistry, Chemistry, Biology or related field Exp: 0-1+ year |
The Microbiology Analyst I will be responsible for assisting the QC microbiological aspects of cGMP compliance and testing at the FujiFilm Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory. | 2/16/2023 |
| 5212 | Generation Bio Cambridge, MA Associate / Senior Associate Scientist, Preclinical Research S. or M.S. Exp: 1 year |
Generation Bio is seeking an energetic and adaptable (Sr.) Associate Scientist to join our Preclinical Research Team, focusing on the liver platforms. This lab-based position will include both in-vitro and ex-vivo assay work, both routine and development. The ideal candidate will have a background with plate-based assays, assay development, mammalian cell culture and in-vitro studies. This role will be responsible for implementing cell-based and ex-vivo assays to characterize gene therapy candidates for a range of implications. | 2/16/2023 |
| 5213 | Gritstone Technology Cambridge, MA MOLECULAR TECHNOLOGY ASSOCIATE I/II Bachelor’s degree (or equivalent) in scientific discipline or a health-related field Exp: 0-2+ years |
The primary role of the Molecular Technology Associate I/II is to perform patient processing using established histology, and next-generation sequencing assays in the GMP Next Generation Sequencing (NGS) laboratory. This team is responsible for the GMP compliant processing of cancer patient samples through nucleic acid extraction and next generation sequencing. The ideal candidate will have patient-centric approach and experience in a regulated environment (CLIA/CAP, cGMP) and will be expected to maintain batch record reports, consumable inventory, equipment maintenance and calibration to maintain quality control and compliance. Individuals with experience as a Clinical Lab Technologist or Molecular Technologist are encouraged to apply. | 2/16/2023 |
| 5214 | Gritstone Technology Cambridge, MA RESEARCH ASSOCIATE I/II, NGS PROCESS DEVELOPMENT (Contractor) Bachelor’s degree (or equivalent) in scientific discipline or a health-related field Exp: 1+ years |
We are seeking a highly motivated, collaborative Research Associate I/II (Contractor) to support our NGS Process Development and Automation team in Cambridge, MA. The ideal candidate will have experience in a high throughput NGS laboratory setting and/or familiarity working in a regulated environment (CLIA/CAP, cGMP). Individuals with experience in cell culture, or as a Clinical Lab Technologist/Molecular Technologist are encouraged to apply. | 2/16/2023 |
| 5215 | Gritstone Technology Emeryville, CA RESEARCH ASSOCIATE I/II, VACCINE TECHNOLOGY Bachelor’s degree (or equivalent) in a scientific discipline or a health-related field Exp: RA I: 1+ year |
We are looking for an enthusiastic and flexible team player who will thrive in a fast-paced, dynamic, and highly collaborative environment. This individual will work in the molecular biology and vaccine technologies group and contribute to the development of novel viral and nucleic acid-based vaccines to meet unmet infectious disease and oncology needs. | 2/16/2023 |
| 5216 | Haemonetics Boston, MA Engineer, Disposables R&D Bachelor's Degree required in Engineering. Exp: 0-2 years |
Applies state of the art techniques in the area of expertise to sustain and/or develop new or improved products and processes. May lead small projects with moderately complex features under manager supervision. Plans, schedules and leads cross-functional team in detailed phases of the engineering work on a project. Must have experience or training and demonstrate proficiency in engineering disciplines (e.g. computer aided design, total quality management (6Sigma), statistical methods, materials science, design of experiments, design controls) and metrology. Must possess knowledge of related disciplines. | 2/16/2023 |
| 5217 | HemoSonics Raleigh-Durham-Chapel Hill, NC Manufacturing Technician Bachelor’s degree in Engineering technical field Exp: 1+ years |
The Manufacturing Technician will be responsible for building Instruments and the associated subassemblies by following the appropriate Work Instructions and Standard Operating Procedures within Instrument Manufacturing. This position will work with a team of Manufacturing Technicians and Engineers to provide input and support for device diagnostics and improvements as required. | 2/16/2023 |
| 5218 | HemoSonics Raleigh-Durham-Chapel Hill, NC Manufacturing Technician Bachelor’s degree in Engineering technical field Exp: 1+ years |
The Manufacturing Technician will be responsible for building Instruments and the associated subassemblies by following the appropriate Work Instructions and Standard Operating Procedures within Instrument Manufacturing. This position will work with a team of Manufacturing Technicians and Engineers to provide input and support for device diagnostics and improvements as required. | 2/17/2023 |
| 5219 | HighRes Biosolutions Beverly, MA Manufacturing Engineer I Bachelor's degree in engineering Exp: 0-3 years |
The Manufacturing Engineer I will develop and maintain methods, processes, and equipment necessary to achieve manufacturing and quality objectives. They will work with engineering to specify, build, test, and challenge new and existing product designs to improve efficiency, reliability, serviceability, manufacturability, and cost. The ideal candidate will be a self-starter who is comfortable working in a dynamic, team-based environment to reach common objectives with aggressive schedules. This role reports to our Manufacturing Engineering Manager. | 2/17/2023 |
| 5220 | HighRes Biosolutions Beverly, MA Associate System Design Engineer BS in Mechanical Engineering. Exp: 0-2 years |
As a Systems Design Engineer at HighRes Biosolutions, you will be heavily involved with all elements of our custom systems product life cycle. Youll work closely with the sales and applications team to turn a customers needs into an automated solution. Additionally, youll work closely with the operations team to turn your designs into fully functional systems. The systems you design will be used by top pharmaceutical and biotech companies around the world to help improve human health. The qualified candidate will have strong design capabilities with SolidWorks. A product development background for lab, medical or consumer products is beneficial. | 2/17/2023 |
| 5221 | HistoTox Labs Evansville, IN Histology Technician I Associate or bachelor’s degree in science related field Exp: 1+ years |
Perform diversified laboratory procedures and operations in the area assigned. | 2/17/2023 |
| 5222 | HistoTox Labs Westminister, CO Laboratory Animal Care Technician I College courses and or Associates or Bachelor’s degree in Animal Science or Husbandry are highly desirable. Exp: 0-3 years |
The ACT I is responsible for providing exceptional animal care to the research animals at Inotiv. This includes performing daily husbandry and care and of laboratory animals in a research environment as well as sanitization and preparation of animal housing equipment, including operation of a large bulk rack washer. The ACT I may be responsible for performing animal technical procedures and providing animal study support with supervision. The ACT I will work as part of a team conducting routine procedures required for vivarium operation. Individuals must demonstrate strong communication skills and be able to work efficiently in individual and team settings. | 2/17/2023 |
| 5223 | HistoTox Labs Rockville, MD Associate Scientist II BSc or MSc in Immunology, molecular biology, bioanalytical chemistry, drug metabolism, pharmacokinetics, or related science. Exp: 1-3 years |
The associate scientists should have knowledge and experience in ligand binding assay techniques, e.g., ELISA, MSD, Luminex, cell-based assays for PK and Immunogenicity determinations, or knowledge of PCR, DNA, RNA analysis, as well as flow cytometry. Due to the different techniques involved, some associate scientists would need essential experience in PCR, DNA, RNA, and flow cytometry analysis with a working knowledge of ligand binding assay techniques, e.g., ELISA (HELISA, etc.), MSD, Luminex, cell-based assays for PK and Immunogenicity determinations and LC-MS/MS. Depending on their experience and capabilities they will be placed in the different sections. | 2/17/2023 |
| 5224 | Ifyber Ithaca, NY Laboratory Technician BS degree Exp: 1 year (more preferred) |
The Laboratory Technician will execute on experimental plans at the interface between chemistry, biology, and materials science and support a variety of programs that will require experience and/or the ability to follow detailed protocols, learn and execute bench skills, and adhere to applicable regulatory requirements. The Laboratory Technician will execute on experimental plans at the interface between chemistry, biology, and materials science and support a variety of programs that will require experience and/or the ability to follow detailed protocols, learn and execute bench skills, and adhere to applicable regulatory requirements. | 2/17/2023 |
| 5225 | Immuneering San Diego, CA Research Associate/Senior Research Associate M.S. in a scientific discipline. Exp: 1+ years |
We have two immediate openings for a full-time Research Associate/Senior Research Associate. The ideal candidate is quality and process-oriented, flexible and must enjoy the challenges of working in a fast-paced, biotechnology company with diverse people and drug programs. The Senior Research Associate is responsible for performing and collaboratively designing research and development experiments for projects and products within discovery/translational research teams. Regularly exercises technical discretion in the design, execution and interpretation of experiments that contribute to project goals. Contributes to project process within scientific discipline through innovative research. | 2/17/2023 |
| 5226 | Imperative Care Campbell, CA Quality Engineer II Bachelor’s degree in Engineering or related discipline Master’s degree. Exp: BS: 1+ years ; MS: 0+ years |
This position provides Quality Engineering support in the development, manufacture, and distribution of Imperative Care’s medical device products consistent with the Company’s Quality Policy and Quality Objectives. | 2/17/2023 |
| 5227 | Indigo Biosciences State College, PA Associate Scientist Master’s Degree in a relevant field of the biological sciences Exp: 0+ years |
The execution of experiments aimed at developing, optimizing, and validating new mammalian cell-based assays for INDIGO’s products and services portfolios. The large-scale manufacturing of mammalian reporter cells and assay kit components Performing routine quality QA testing of inventory stocks and executing inventory control policies to ensure the availability and integrity of INDIGO products. Assist Senior Scientists in the execution of contract service studies for INDIGO’s various biopharma, biotech, academic, and governmental clients. Execute ‘Inventory Control’ policies to ensure the availability and integrity of INDIGO Products. Routine Quality Assurance (QA) testing of Inventory stocks, and remanufacturing materials as needed to maintain appropriate levels of Inventory materials. Maintain and generate DNA stocks, as needed (plasmid purifications and gel analyses) Maintain an up-to-date, neat, orderly notebook according to the policies of the company. Contribute to weekly lab meetings. Associate Scientists are expected to present and interpret their own data for the Team, as well as to propose ‘next steps’ to advance their project. Further, Associate Scientists are expected to be fully intellectually engaged in critical evaluating other’s experimental data, as well as in the group processes of trouble-shoot technical problems, ‘brain storming’ the application of new or alternative technologies, and formulating and prioritizing sound experimental strategies to benefit individual & Team objectives. | 2/17/2023 |
| 5228 | IntelliSyn R&D Waltham, MA Research Associate BS or MS in Chemistry or related subject Exp: 6 months-2 years |
X-Chem is seeking a candidate for the position of Research Associate, Library Synthesis in its Discovery Chemistry group. X-Chem is a drug discovery company that uses DNA-encoded library (DEL) technology to discover leads for therapeutic targets. As a world leader in DEL technology, X-Chem collaborates with numerous pharmaceutical and biotechnology companies, resulting in over 70 licensed programs to date. | 2/17/2023 |
| 5229 | Pace Analytical Greenfield, IN Biologist Bachelor's degree in Biology Exp: 0+ years |
Candidate will use their skills and knowledge in Biology/Microbiology to support development of new products. | 2/17/2023 |
| 5230 | Pace Analytical Minneapolis, MN GC LC Chemist - Analytical Instrument Specialist BS degree in chemistry or related science Exp: 6 months - 2 years |
Working in our Technical Field Services (TFS) division allows chemists to perform hands-on work and interact directly with our clients. We specialize in servicing instrumentation such as GC, GC/MS, LC, LC/MS, IC, and Dissolution. While the instrumentation is complex, TFS has an extensive training program for new employees, as well as ongoing training to maintain the capabilities of our service staff. Our TFS Specialists have multifaceted skill sets including: strong technical aptitude, customer service, and problem resolution techniques. Additionally, we have been providing service to customers for eighteen years, achieving steady growth on an annual basis, which allows multiple advancement opportunities in MN, IL, IN, TX, and CA. Instrument Services Specialists are responsible for providing technical solutions and an advanced level of instrument support services to customers of TFS, including external clients, laboratory chemists within the Pace lab system, and departmental coworkers. They also provide our customers with a variety of support services associated with their analytical instrumentation. These services include routine maintenance, operational and performance testing, hardware and software troubleshooting, instrument repair, and personnel training.Working in our Technical Field Services (TFS) division allows chemists to perform hands-on work and interact directly with our clients. We specialize in servicing instrumentation such as GC, GC/MS, LC, LC/MS, IC, and Dissolution. While the instrumentation is complex, TFS has an extensive training program for new employees, as well as ongoing training to maintain the capabilities of our service staff. Our TFS Specialists have multifaceted skill sets including: strong technical aptitude, customer service, and problem resolution techniques. Additionally, we have been providing service to customers for eighteen years, achieving steady growth on an annual basis, which allows multiple advancement opportunities in MN, IL, IN, TX, and CA. | 2/17/2023 |
| 5231 | Pace Analytical Naperville, IL Scientist (Chemist, Lab Technician, Biologist) Bachelor's degree in Biology, Chemistry, Physics, and other related science. Exp: 6 months - 2 years |
Join us at Pace, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. This is a lab based position. The candidate will be conducting various physical and chemical tests to assist scientists in making qualitative and quantitative analyses. Role may involve wet bench lab work, chemical handling, preparation of solutions/dilutions as well as routine analytical characterization and data analysis. Various shifts may be available. These positions are contracted positions which may last up to 12 months. | 2/17/2023 |
| 5232 | Pace Analytical Eagan, MN Scientist (Chemists, Lab Technicians) Bachelor's degree in Biology, Chemistry, Physics, and other related science. Exp: 6 months - 2 years |
Join us at Pace, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. This is a lab based position. The candidate will be conducting various physical and chemical tests to assist scientists in making qualitative and quantitative analyses. Role may involve wet bench lab work, chemical handling, preparation of solutions/dilutions as well as routine analytical characterization and data analysis. Various shifts may be available. Several locations within the Minneapolis area and surrounding cities. These positions are contracted positions which may last up to 12 months. | 2/17/2023 |
| 5233 | Pace Analytical Chicago, IL Laboratory Technician Bachelors Degree in a science; Chemistry is preferred Exp: 1-2 years |
Join us as a Laboratory Technician, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace® The laboratory technician will primarily help out a busy lab doing data entry. 70% of the role is expceted to be data entry. Note: This position is expected to last 6 months. | 2/17/2023 |
| 5234 | Invicro New Haven, CT Associate Scientist - Radiochemistry Bachelor’s level degree in analytical chemistry Exp: 0-3 years |
We are seeking a motivated and dynamic Analytical Chemist who can adapt to the fast speed and highly competitive environment. The candidate must have strong analytical chemistry experience to perform all the quality testing for radiopharmaceuticals produced at Invicro. Invicro does contract research focusing on the development of short half liferadiotracers for PET and SPECT imaging. The Analytical Chemist's primary purpose is to conduct the quality control testing of the radiotracers to ensure that all release criteria for human use are met. A strong background in HPLC and GC are required. Knowledge in aseptic techniques and cGMP is preferred. | 2/17/2023 |
| 5235 | Invicro Needham, MA Laboratory Assistant, Advanced Pathology Services Bachelor’s degree in a relevant biological science. Exp: 1-2 years’ |
Make an impact at a dynamic and growing company! Invicro seeks a Laboratory Assistant for Advanced Pathology Services to support for all routine Histology and IHC work pertaining to delivery of CAP/CLIA and GLP-like oriented lab services offered to external partners, including BioPharma, Academia, and Oncology Research Centers. Our laboratory performs high complexity immunohistochemistry and other advanced tissue analysis approaches unique to Invicro. This individual should enjoy challenging and analytical work and be motivated by the idea that together we can accomplish great things and make a positive contribution to society through our mission. | 2/17/2023 |
| 5236 | Vigene Biosciences Memphis, TN Manufacturing Associate - Cell Therapy 1 AS or BS in a scientific field strongly preferred. Exp: Zero to 1 year |
We are seeking a Manufacturing Associate for our Cell Therapy Manufacturing Facility located in Memphis, TN. Work Schedule: Sunday-Wednesday Work Hours: 7:30 a.m-6:00 p.m. (CST) The Manufacturing Associate I is responsible for performing various manufacturing activities related to the start- up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to work night, weekends, and holidays. Must be able to meet physical requirements established in this job description. | 2/17/2023 |
| 5237 | Vigene Biosciences Memphis, TN Process Engineer I BS / MS / PhD in engineering or life sciences Exp: 1 year |
We are seeking a Process Engineer I for our Cell Therapy Manufacturing Facility located Memphis, TN. The Process Engineer I will provide equipment and facility technical support for incoming technology transfers of client manufacturing processes for advanced cell therapies. This role will participate in the transfer process and ensuring that the knowledge transfer to the manufacturing and supporting groups is efficient and effective. Additionally, this role will lead process equipment improvements, assessments, investigations, and implementations as governed by the site procedures and/or client requirements. | 2/17/2023 |
| 5238 | Vigene Biosciences Memphis, TN Quality Control Analyst I - Microbiology (EG) Bachelor's degree in Biology or relevant scientific discipline required. Exp: 0-2 years |
The Quality Control Analyst I for the QC Microbiology Department will be responsible for performing processing of routine environmental monitoring samples, product-release testing, and raw material testing. The position requires the utmost attention to detail, good organizational skills, computer proficiency, and a basic understanding of microbiology and laboratory instrumentation. In addition, effective communication skills and the ability to function in a fast-paced, highly technical environment with minimal supervision are essential for success. | 2/17/2023 |
| 5239 | Vigene Biosciences Memphis, TN Biomanufacturing Technician-Shift A (Sunday-Wed/7:30 a.m.-6:00 p.m.) EG AS or BS in a scientific field strongly preferred. Exp: Zero to 1 year |
We are seeking a Manufacturing Associate for our Cell Therapy Manufacturing Facility located in Memphis, TN. Work Schedule: Sunday-Wednesday Work Hours: 7:30 a.m-6:00 p.m. (CST) The Manufacturing Associate I is responsible for performing various manufacturing activities related to the start- up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to work night, weekends, and holidays. Must be able to meet physical requirements established in this job description. | 2/17/2023 |
| 5240 | Organogenesis Canton, MA Production Associate I/II- Apligraf (Sunday-Thursday) Associates or Bachelor’s degree in biology or related science Exp: 0 - 2 years |
This is an entry level position. The Associate will perform all activities involved in the aseptic processing of a living product (Apligraf), under the direct supervision of the Apligraf Team Leader/Apligraf Supervisor/Manager. The Apligraf Associate I will support the Apligraf Manufacturing department by performing the tasks that will assure the safe and timely processing of Apligraf, working in both a Class 100 and Class 10K cleanroom. | 2/7/2023 |
| 5241 | Organogenesis Canton, MA Quality Control Analyst I/II-Microbiology AS or BS degree in a Biology, Chemistry or equivalent QC related Exp: One (1) or more years |
The purpose of this position is the performance and reporting of microbiological testing for product release as well as environmental monitoring of all areas of the manufacturing facility, water sample collection and testing, compilation and entry of environmental monitoring data. The position ensures that the company goals for timely product testing are accomplished by being directly involved in the production of test results for product release and investigations. Other responsibilities or tasks as deemed necessary from time to time by the area’s supervisor. Some holiday work required. | 2/7/2023 |
| 5242 | Organogenesis Canton, MA Production Associate I/II- Apligraf (Sunday-Thursday) Associates or Bachelor’s degree in biology or related science Exp: 0 - 2 years |
This is an entry level position. The Associate will perform all activities involved in the aseptic processing of a living product (Apligraf), under the direct supervision of the Apligraf Team Leader/Apligraf Supervisor/Manager. The Apligraf Associate I will support the Apligraf Manufacturing department by performing the tasks that will assure the safe and timely processing of Apligraf, working in both a Class 100 and Class 10K cleanroom. | 2/7/2023 |
| 5243 | Meridian Medical Technologies Kalamazoo, MI Associate, Process Engineer Vaccine Injectable Manufacturing bachelor's degree Exp: 0-2+ years |
The Associate Process Engineer Vaccine Inj Manufacturing position will support projects and day to day operation of Sterile Vaccine Manufacturing Operations. This may include product transfer projects, cost improvement projects, capital equipment installations, Right First-Time initiatives, and safety and compliance driven initiatives for Drug Product Operations. | 2/7/2023 |
| 5244 | Meridian Medical Technologies Sanford, NC QA Associate - 2nd Shift Bachelor's degree n Biology, Chemistry, Engineering or related Technical Physical Science. Exp: 0-2 years |
You will be a member of Pfizer’s dedicated and highly effective Manufacturing Quality Assurance operations team. You will evaluate and review manufacturing activities in support of clinical and commercial batch production. Your expertise will help in identifying deviations from established standards, in the manufacturing of clinical and commercial batches. You will make sure that product and process documents match the specifications based on established sampling and statistical process control procedures. As a QA Associate, your focus on the job will contribute to achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues. | 2/7/2023 |
| 5245 | Meridian Medical Technologies Pearl River, NY Associate Scientist, Immunology Master’s degree Exp: 1 year |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role to generate high-quality immunoassay data in a regulated Good Laboratory Practices (GLP) setting to support Pfizer’s vaccine programs according to Standard Operating Procedures. You will support the technology transfer and integration of new laboratory immunoassays into the cGLP space, support assay validation projects and monitor immunoassay lifecycle. In addition, you will also support throughput activities and provide testing support for clinical and non-clinical research programs. Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. | 2/7/2023 |
| 5246 | Meridian Medical Technologies Pearl River, NY Associate Scientist NGS BS Degree in Molecular biology, Virology, Immunology, or related scientific field Exp: 1-3 years |
We are seeking a highly motivated associate scientist with exceptional molecular biology knowledge to join Viral Vaccines department in Pearl River, NY. The ideal candidate will have some Next Generation Sequencing lab experience or have strong interests learning the technology and apply the technology to mRNA-based vaccine research and development. This role is wet laboratory based. The successful candidate will interface with a diverse set of colleagues to support the application of NGS technologies. You will be required to perform assigned lab experiments and record experiments details with E-notebook in a timely manner. You also be required to place and track reagents inventory, lab equipment operation and maintenance. In order to maintain compliance of regulated environment, you also will be responsible for the preparation and maintenance of associated documents and reports. Meticulous attention to detail, proficient reasoning and problem-solving skills and critical thinking are required. In addition to follow the established laboratory procedures, the individual should possess the curiosity and enthusiasm about the developmental work knowledge. The successful candidate should have solid background in DNA/RNA characteristics, qPCR assay development, genetics, and principles of genomic alterations. | 2/7/2023 |
| 5247 | Meridian Medical Technologies Pearl River, NY Associate Scientist, Molecular Testing Bachelor’s degree in a relevant field of science (E.g., immunology, bacteriology, or microbiology) Exp: 0 – 2 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role of generating high-quality molecular diagnostic data to support vaccine clinical development in a high‑throughput setting. The responsibilities include but are not limited to, performing manual and/or robotic molecular diagnostic testing, such as polymerase chain reaction (PCR). Other laboratory support activities include preparation of buffers and media, qualification of assay reagents, qualification and validation of assays, and other duties assigned as necessary. The incumbent will work in a team setting and will share roles and responsibilities as assigned by the Team Leader/Manager. Strong oral and written communication skills are essential. The position requires keeping current on documentation related to sample testing and assay development activities. As an integral member of this dynamic team, the incumbent must have a strong work ethic and be highly collaborative with other group members. The incumbent must be satisfied with repetitive and routine tasks, as this is a lab-based role. In addition, the incumbent must use good documentation practices, follow established safety policies and procedures, and perform all work in a compliant manner according to relevant SOP guidelines and GCLP and/or GMP guidelines, as required. | 2/7/2023 |
| 5248 | Meridian Medical Technologies Pearl River, NY Associate Scientist Bachelor’s degree in a relevant field of science (E.g., immunology, bacteriology, or microbiology) Exp: 0 – 2 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role of generating high-quality molecular diagnostic data to support vaccine clinical development in a high‑throughput setting. The responsibilities include but are not limited to, performing manual and/or robotic molecular diagnostic testing, such as polymerase chain reaction (PCR). Other laboratory support activities include preparation of buffers and media, qualification of assay reagents, qualification and validation of assays, and other duties assigned as necessary. The incumbent will work in a team setting and will share roles and responsibilities as assigned by the Team Leader/Manager. Strong oral and written communication skills are essential. The position requires keeping current on documentation related to sample testing and assay development activities. As an integral member of this dynamic team, the incumbent must have a strong work ethic and be highly collaborative with other group members. The incumbent must be satisfied with repetitive and routine tasks, as this is a lab-based role. In addition, the incumbent must use good documentation practices, follow established safety policies and procedures, and perform all work in a compliant manner according to relevant SOP guidelines and GCLP and/or GMP guidelines, as required. | 2/7/2023 |
| 5249 | Meridian Medical Technologies Pearl River, NY Associate Scientist Molecular Testing Bachelor’s degree in a relevant field of science (E.g., immunology, bacteriology, or microbiology) Exp: 0 – 2 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role of generating high-quality molecular diagnostic data to support vaccine clinical development in a high‑throughput setting. The responsibilities include but are not limited to, performing manual and/or robotic molecular diagnostic testing, such as polymerase chain reaction (PCR). Other laboratory support activities include preparation of buffers and media, qualification of assay reagents, qualification and validation of assays, and other duties assigned as necessary. The incumbent will work in a team setting and will share roles and responsibilities as assigned by the Team Leader/Manager. Strong oral and written communication skills are essential. The position requires keeping current on documentation related to sample testing and assay development activities. As an integral member of this dynamic team, the incumbent must have a strong work ethic and be highly collaborative with other group members. The incumbent must be satisfied with repetitive and routine tasks, as this is a lab-based role. In addition, the incumbent must use good documentation practices, follow established safety policies and procedures, and perform all work in a compliant manner according to relevant SOP guidelines and GCLP and/or GMP guidelines, as required. | 2/7/2023 |
| 5250 | Regeneron Tarrytown, NY Temp - Research Pharmacokinetics BS degree in biology or a related field Exp: 1-3 years |
Regeneron's Research Pharmacokinetics team within our Therapeutic Proteins organization is looking for an energetic Temporary Associate to join the team. In this exciting role, you will be expected to provide sample analysis assistance of timeline driven experiments. | 2/9/2023 |
| 5251 | Regeneron Tarrytown, NY Associate Scientist, Protein Expression Sciences BS or MS in a scientific field Exp: 0-3 years |
We are seeking a Associate Scientist to join the Protein Expression Sciences team. In this role, you will be responsible for generating manufacturing grade clinical cell lines for production of therapeutic antibodies to support the Regeneron pipeline. | 2/9/2023 |
| 5252 | Regeneron Tarrytown, NY Associate Scientist, Immunology MS Exp: 1+ years’ |
VelocImmune (VI) Next is a technology development group at Regeneron that invents and develops state-of-the-art tools for biologic drug discovery. We are seeking a motivated, highly organized scientist to support our investigations of new antibody and cell-based therapies. This is an opportunity for a researcher with strong molecular & immunology skills to contribute to the development of industry-leading technologies and medicines. | 2/9/2023 |
| 5253 | Regeneron Tarrytown, NY Associate Scientist, Immunology (In-Vivo) BS/MS Exp: 1-3 years |
We are seeking a motivated Associate Scientist to join a highly interactive immunology team. You will work on a team that develops and performs in vivo models for different asthma/allergy/autoimmunity diseases. This work will support to screen antibody candidates in mouse models, provide cytokine profiles after antibody treatment. | 2/9/2023 |
| 5254 | Regeneron Tarrytown, NY Associate Scientist, Clinical Bioanalysis BS degree or MS degree in a scientific field Exp: 0-3+ years |
Regeneron's Clinical Bioanalysis group, located in Tarrytown NY, is seeking a Associate Scientist. | 2/9/2023 |
| 5255 | Regeneron Tarrytown, NY Associate Scientist (Cell Culture for Therapeutic Antibody Discovery) BS degree or MS degree in a scientific field Exp: 0-3+ years |
Regeneron's Protein Expression Sciences (PES) group, located in Tarrytown, NY, is seeking a motivated Associate Scientist to join our human antibody isolation team, which contributed to the development of Regeneron’s Sars-Cov2 antibody cocktail (REGEN-COV). You will play an integral part in the identification of antibodies to treat diseases with unmet medical needs. The primary functions of this position are the isolation of monoclonal antibodies from human donors against diverse disease targets (eg. infections, immune disorders, etc) and the development of new antibody isolation technologies. Some experiments will require mice work such as organ harvesting and dissection. | 2/9/2023 |
| 5256 | Steris St Louis, MO Associate Scientist I- Microbiology Bachelor degree in Biology, Microbiology, Molecular Biology is preferred. Exp: 0-5 years |
Position Description Under close direction of supervising scientist or manager, completes assigned laboratory studies/tasks which include: - Accurate and thorough recording of raw data. - Mathematical analysis and data compilation. - Discussion of results. | 2/9/2023 |
| 5257 | West Pharma Exton, PA Associate Scientist, 2nd Shift, Lab BS in Chemistry or related technical degree Exp: 0 - 3 Years |
In this role, you will be responsible for performing testing for both internal and external customers in a cGMP environment, while integrating into a diverse technical team. | 2/9/2023 |
| 5258 | West Pharma Exton, PA Associate Scientist, Raw Materials Lab BS in Chemistry or related technical degree. Exp: 0-3 years |
In this role, you will be responsible for performing testing for both internal and external customers in a cGMP environment. | 2/9/2023 |
| 5259 | West Pharma Exton, PA Associate Scientist Lab Release BS in Chemistry or related technical degree. Exp: 0-3 years |
In this role, you will be responsible for performing testing for both internal and external customers in a cGMP environment. | 2/9/2023 |
| 5260 | West Pharma Kinston, NC Lab Associate, Kinston Bachelor’s degree in Microbiology or Science related discipline. Exp: 1-3 years |
In this role you will perform all required routine testing (Bioburden Silicone, Particle, Endotoxin) to support product release, including water testing, environmental monitoring. Support other laboratory functions as needed | 2/9/2023 |
| 5261 | West Pharma Exton, PA Associate Scientist Lab Release BS in Chemistry or related technical degree. Exp: 0-3 years |
In this role, you will be responsible for performing testing for both internal and external customers in a cGMP environment. | 2/9/2023 |
| 5262 | Acrotech Biopharma East Windsor, NJ MICROBIOLOGIST Master of Science Exp: Up to 3 years |
Microbiologist will perform a variety of Microbiology testing to assess the strength, identity and purity of test samples and/or materials. The Microbiologist will work as a member of team to effectively plan and Microbiology testing using established (official in USP and/or in-house) test procedures. The Microbiology may execute 90% - 100% of their work at the bench level. | 2/9/2023 |
| 5263 | Cell Signaling Technology Beverly, MA Senior Research Associate Masters degree in Biological Sciences or related degree Exp: 1-2 years |
The Multiplex Assays Development team is growing, and we are looking for a highly motivated Senior Research Associate who is passionate about collaborating with a team of scientists to develop and commercialize complex novel technologies for visualizing biology. A successful candidate will have the opportunity to independently prepare and maintain an inventory of reagents and buffers in order to perform multiplex immunofluorescence experiments, analyze data, and communicate results to the team. This cross-functional, team-oriented position requires strong organizational skills, exceptional attention to detail, and robust scientific communication skills. | 2/9/2023 |
| 5264 | Cell Signaling Technology Beverly, MA Senior Research Associate Masters degree in Biological Sciences or related degree Exp: 1-2 years |
The Multiplex Assays Development team is growing, and we are looking for a highly motivated Senior Research Associate who is passionate about collaborating with a team of scientists to develop and commercialize complex novel technologies for visualizing biology. A successful candidate will have the opportunity to independently prepare and maintain an inventory of reagents and buffers in order to perform multiplex immunofluorescence experiments, analyze data, and communicate results to the team. This cross-functional, team-oriented position requires strong organizational skills, exceptional attention to detail, and robust scientific communication skills. | 2/9/2023 |
| 5265 | Cell Signaling Technology Danvers, MA Research Associate I Bachelors in Biological Sciences (Biochemistry, Biotechnology or related discipline). Exp: 1 year |
The Custom Conjugation team is growing, and we are looking for a highly motivated Research Associate. The main responsibility of this position is the conjugation of antibodies to fluorescent dyes, oligonucleotides, beads, HRP, biotin, PE, PE tandem dyes and utilization of the following techniques: protein purification and determination, western blotting and immunoprecipitation. | 2/9/2023 |
| 5266 | Cell Signaling Technology Beverly, MA Lab Technician II BS/BA Degree in Chemistry or related science Exp: 0-2 years |
The Lab Technician II Buffer Prep is primarily responsible for following standard operating procedures, with increasingly limited supervision and as part of a team, to provide high quality chemical solutions, highly responsive service and to perform a wide variety of basic laboratory tasks in support of CSTs Production, Development, and Research laboratories. | 2/9/2023 |
| 5267 | Civetta Therapeutics Cambridge, MA Cell Biology Research Associate BS in Biology, Molecular Biology, Biochemistry, or related Life Science discipline Exp: 1-3 years |
We are seeking a highly-motivated Research Scientist to help support our chemical biology efforts at Civetta. This candidate will help us discover small molecule modulators of beta-propeller proteins, support validation of new targets, and help propel our ongoing drug discovery programs. This is an excellent opportunity for individuals looking to work in a fast-paced, dynamic biotech environment. | 2/9/2023 |
| 5268 | WuXi Apptec Plainsboro, NJ Associate Scientist I Bachelor’s degree in chemistry, biology, or a related discipline Exp: 0-2 years |
The Associate Scientist I will be primarily responsible for the bioanalysis of samples at WuXi AppTec and will follow validated or experimental bioanalytical procedures, to perform assays and support pharmaceutical product development, testing and evaluation in a GLP regulatory laboratory environment. The employee will use state-of-the-art technologies/techniques to perform top-quality sample analysis and testing for key pharmaceutical and biotech clients across the industry. | 2/9/2023 |
| 5269 | WuXi Apptec San Diego, CA Research Associate II - In Vivo Pharmacology Master degree in Molecular and Cell Biology or Bachelor degree Exp: 1 -2 year |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly skilled and motivated Research Associate II to support our in vivo pharmacology team for various projects. | 2/9/2023 |
| 5270 | WuXi Apptec Cranbury, NJ Associate Scientist I - PKPD Bachelor’s degree in animal science, biology, or a related discipline. Exp: 0-3 years |
Plans and carries out in vivo experiments and associated research assignments in rodents. Maintains the vivarium, labs, and program to AAALAC standards. | 2/9/2023 |
| 5271 | Catamaran Bio Boston, MA Research Associate / Senior Research Associate, Cell Culture BS or certificate in biology, biotechnology, or equivalent/related disciplines. Exp: 1-5 years |
Catamaran is seeking an experienced, hands-on Research Associate / Senior Research Associate to support Catamaran’s development of an allogeneic NK cell drug product. The successful candidate will be responsible for generating and maintaining stocks of cell lines used for in vitro and in vivo assays, including feeder cells, tumor cell lines, NK cells and genetically modified cells. This work involves cell isolation, expansion, engineering, harvest and cryopreservation. This role will require collaborating extensively with Research and CMC teams. The ideal candidate has relevant experience in cell culture of primary human cells and cell lines, and is excited to join a small, fast-paced team with a “can-do” attitude to drive forward our new cell therapy platform. | 2/9/2023 |
| 5272 | Catamaran Bio Boston, MA Research Associate/Senior Research Associate, Cell Process Bachelors or master’s degree in chemical engineering, immunology, biology, synthetic biology, chemical biology, biochemistry, pharmaceutical sciences, Exp: 0-2 years’ |
The Cell Process Team is seeking a talented, diligent, and collaborative research associate to execute and design cell expansion process activities for the advancement of our best-in-class CAR-NK Cell Therapies for Oncology and other diseases. Cell Process works to ingeniously solve the challenges associated with the allogeneic manufacture of CAR-NK cell therapies including cell isolation/enrichment; cell engineering and gene editing; and cell expansion. They will be responsible for the operation of a clinical-scale bioreactor process design for the expansion of clinical CAR-NK candidates, execution of cell-based assays for in-process characterization, and technical process transfer to internal and external manufacturing sites in support of Phase 1 clinical activities. The ideal candidate is a self-motivated and technically competent process development scientist or engineer with an interest in bioreactor design and control, who is excited to join a small, fast-paced team with a “can-do” attitude to drive forward our new cell therapy platform. This is a unique opportunity to realize the promise of allogeneic cell therapy manufacturing paradigms and bring the TAILWIND platform to life at a clinical scale. | 2/9/2023 |
| 5273 | Cellics Therapeutics San Diego, CA Research Associate, Quality Control (Biologics)– San Diego BS/BA in chemistry, biology, or a related field is required, advanced degrees a plus. Exp: 1-3 years |
Cellics Therapeutics is seeking a Research Associate of Quality Control, reporting to the Director of Analytical Development and QC, to conduct quality control testing of incoming raw materials, in-process, release and stability samples for biologics drug intermediates, drug substances, and drug products. The candidate also performs the environmental monitoring for manufacturing facilities | 2/9/2023 |
| 5274 | Charter Medical Winston-Salem, NC Quality Engineer Bachelor of Science degree in technical field (life science, physical science, engineering or related field) required. Exp: 1-3 years |
Conducts investigations and Root Cause Analysis derived from Customer Complaints, CAPAs, Trending, Out of Specifications, Nonconformances, etc. Interfaces with customers to provide reports, data and/or technical support for Products, Complaints, Change Control and Customer Notifications. Develops and monitors implementation of Protocols for product evaluation as required. Creates, edits and/or revises Test Method Validations, SOPs, WIs, Product Specifications as required. Performs Supplier Quality Audits, SCARs (Supplier Corrective Actions) as well as Notifications issuance. Assists with Corrective Action system, including but not limited to, administrative duties for database maintenance, serve as CAPA team member or CAPA team leader, facilitate root cause analysis with CAPA teams, ensure CAPA documentation is complete and accurate, perform follow-up evaluation of CAPA effectiveness, and provide trending reports. Addresses Customer Complaints, derived investigations, corrective actions implementation, and reporting. Assists with hosting, preparing and coordinating external audits and/or Technical Visits as requested. | 2/9/2023 |
| 5275 | Cogent Professionals Indianapolis, IN Experienced Pharmaceutical Analytical Chemist MS - Chemistry Exp: 1-3 years |
We currently have a role available for an Experienced Pharmaceutical Analytical Chemist. Job duties include, but are not limited to: Purification using one or more of the following: Normal phase purification using Teledyne ISCO Combiflash and/or Torrent systems Normal phase method development using TLC Reversed phase purification using Teledyne ISCO Combiflash, ACCQ Prep, and EZ Prep flash/HPLC systems Reversed phase purification using Agilent 1100/1200/1260/1290 series Chiral purification using LC and SFC systems Familiarity with ChemStation. Perform instrument maintenance and troubleshooting as needed. | 2/9/2023 |
| 5276 | Debut Technology San Diego, CA Fermentation Technician College-level coursework in general biology, microbiology, and chemistry is preferred Exp: 1-4 years |
The Fermentation Technician will be a critical contributor to our research and production teams by performing various lab support duties. The role requires multiple hands-on tasks, including cleaning and autoclaving glassware and small equipment. | 2/10/2023 |
| 5277 | Decipher Biosciences San Diego, CA Clinical Lab Technician Bachelor’s degree required Exp: 1 years’ |
The Clinical Lab Technician’s primary responsibility is to provide front-line support in the procurement of record of loan (ROL) material and manage chain-of-custody of samples received. This individual must support the Decipher internal and external customers in the routine functions to ensure client satisfaction and appropriate records and materials management are consistently maintained. This individual must work with staff to employ a team approach. Manages patient orders with or without samples and oversees special projects assigned by their supervisor. | 2/10/2023 |
| 5278 | Decipher Biosciences San Diego, CA Research Associate I, Assay Development B.Sci. in biological sciences (or related field) Exp: 1-2 years |
The Research Associate I will support the Assay Development team at Decipher Biosciences; assisting in research, development, and optimization of genomic assays, and supporting general laboratory maintenance and document control. Other responsibilities might be applied as needed. | 2/10/2023 |
| 5279 | Deepcell Menlo Park, CA Research Associate/Senior Research Associate, System Integration Bachelor’s or Master’s degree in Bioengineering, Biomedical Engineering, or similar subject is required, Exp: one year |
Operate and maintain lab instruments, including Deepcell R&D systems; Troubleshoot and optimize components related to Deepcell’s proprietary platform; Perform cell culture protocols. Improve and develop SOPs with consistency and clarity; Execute standard molecular biology techniques; Perform routine laboratory maintenance activities | 2/10/2023 |
| 5280 | Astellas Seattle, WA Research Associate II, Process Development in Seattle, Washington MS Exp: 0-2 years |
The primary purpose of the Research Associate II for Process Development is to execute experiments to improve clinical-grade, gene-editing processes of Universal Donor Cells and to provide data for CMC documents. This Research Associate II role will work as part of a team evaluating processes, and planning/executing experiments to evaluate all aspects of culturing, gene-editing, and processing of pluripotent stem cells. This position will be provided training to perform all required fundamental skills. Will assist with complex laboratory operations, keep appropriate documentation including lab notebooks, batch documentation and experimental summaries. Will be able to execute protocols with minimal guidance and will have the ability to summarize results independently. May assist in generating content and preparing controlled documents and data summaries. This position will acquire further versatility in routine procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. | 1/30/2023 |
| 5281 | Astellas Seattle, WA Research Associate II, Cell Analytics in Seattle, Washington MS Degree Exp: 0-2 years |
We are seeking a highly capable, self-motivated Research Associate II for our Core Technologies Department. This individual will contribute to the molecular engineering and characterization for our gene edited Universal Donor Cells, by utilizing various cell culture techniques. They will work as a key member on a fast paced team to culture pluripotent stem cells as well as run cellular assays to characterize our proprietary Universal Donor Cells. | 1/30/2023 |
| 5282 | Astellas Westborough, MA Research Associate II, Analytical Development in Westborough, Massachusetts MS Exp: 0-2 years |
The Research Associate will support assay development and qualification activities by performing cell culture and wet lab experiments, analyzing data, and drafting protocols, SOPs, and reports. This individual will be expected to execute protocols with some guidance and have the ability to summarize results independently. They will collaborate closely within the team and across functional groups to advance pipeline programs. | 1/30/2023 |
| 5283 | Astellas South San Francisco, CA Research Associate II, Vector Biosciences in South San Francisco, California Master's Degree in Molecular Biology, Cell Biology, Life Sciences Exp: 1+ years |
We are looking for a highly motivated Research Associate to join the Vector Biosciences Group in our South San Francisco R&D labs. This position involves application of multidisciplinary experiments including molecular cloning, cell culture, AAV packaging and purification and other in vitro experiments. | 1/30/2023 |
| 5284 | Astellas South San Francisco, CA Research Associate I/II, Vector Biosciences in South San Francisco, California Master's Degree in Molecular Biology, Biology, Life Sciences or a related discipline Exp: 1+ years |
The Research Associate will support the Vector Biosciences team and assist with the development of novel AAV gene therapy vectors using molecular biology techniques. The Research Associate will be located in our South San Francisco R&D laboratories. | 1/30/2023 |
| 5285 | Astellas Seattle, WA Research Associate II, Clinical Gene Editing in Seattle, Washington MS Exp: 0-2 years |
The primary purpose of the Research Associate II for Clinical Gene Editing is to support the generation of clinical-grade, gene-edited Universal Donor Cells in a controlled manufacturing environment. This Research Associate II role will work as part of a team planning and executing all aspects of gene-editing and engineering of pluripotent stem cells. Will assist with complex laboratory operations, keep appropriate documentation including lab notebooks, batch documentation and experimental summaries. Will be able to execute protocols with minimal guidance and will have the ability to summarize results independently. May assist in generating content and preparing controlled documents and data summaries. This position will acquire further versatility in routine procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. | 1/30/2023 |
| 5286 | Atsena Therapeutics Durham, NC Laboratory Operations Assistant Bachelor’s degree Exp: 1 year |
We are seeking an enthusiastic, highly motivated Lab Operations Assistant to support our company’s growth. The successful candidate will bring experience, knowledge, and best practices and serve as primary backup to the Laboratory Operations Manager to oversee inventory, shipping/receiving, vendor & equipment service calls and general facility oversite. Additionally, this person will provide basic laboratory support to the science teams. We recently moved into a state-of-the-art facility, and this is a great opportunity for building up the function from the ground level. | 1/30/2023 |
| 5287 | Aurora Biolabs San Diego, CA Research Associate I Bachelors or Masters Exp: Entry Level for level I, |
The individual will be a critical part of our products development team, development a new line of recombinant protein products for drug discovery and commercial use. This position requires extensive hands-on experience with a broad range of techniques including protein expression and purification, molecular cloning, PCR, mammalian cell, insect cells and bacterial culture, ELISA, as well as in vitro cell-based/immuno-based assays. | 1/30/2023 |
| 5288 | Avid Bioservices Tustin, CA Biomanufacturing Associate Downstream Purification (Flex Team) Bachelor's degree in a life science field such as Biology or Biotechnology (REQUIRED) Exp: 1+ years |
As a Biotech Manufacturing Associate, you play an integral role in ensuring the on-time delivery of quality biopharmaceutical products. You get to participate in a variety of tasks including purification of biologics, keeping up-to-date GMP documentation, writing reports, ordering materials, and scheduling equipment services. You are conscientious about maintaining strict compliance with GMP manufacturing practices as you adhere to our standard operating procedures. | 1/30/2023 |
| 5289 | Axial Therapeutics Woburn, MA RESEARCH ASSOCIATE/SENIOR RESEARCH ASSOCIATE - BIOSCIENCES Bachelor’s degree in biology, biochemistry, or a related field preferred Exp: 1-3 years |
In this role the Research Associate will support biology as a member of a highly matrixed drug discovery team and will be responsible for the execution and troubleshooting of various cell-based and biochemical assays and experiments. The Research Associate will contribute to drug screening and mechanism-of-action studies for projects in immuno-oncology and neurological diseases and disorders and have opportunities to contribute to new target discovery and validation. This proactive researcher will collaborate with team members, identify opportunities to improve efficiency, share ideas and expertise and contribute to Axial’s creative, dynamic, and collaborative culture. | 1/31/2023 |
| 5290 | Azzur Devens, MA Microbiologist Bachelors of Science or Bachelors of Arts in the field of the life sciences. Masters of Science preferred. Exp: 1-2 years |
Azzur Lab is looking for Microbiologist, who will perform laboratory testing and interacts with clients to interpret their results. The Senior Microbiologist has the responsibility to ensure that laboratory testing is completed in accordance with established methods and protocols. | 1/31/2023 |
| 5291 | Beam Therapeutics RTP, NC Manufacturing Associate (multiple openings) BS, MS a plus, in Life Sciences or Engineering Exp: 0-5 years |
Beam is expanding our geographical footprint to RTP, NC with the recent announcement of a 100,000 square foot manufacturing facility in addition to our laboratory-based facilities located in Cambridge, MA. We are looking for highly energetic Manufacturing Associates to support start-up and scaling of cGMP manufacturing at our new RTP site. Reporting to the Manager of Manufacturing, the successful candidates will provide manufacturing, operational & technical experience around commissioning, training, qualification, and start-up. The ideal candidates will have experience in cell or gene therapy, along with demonstrated ability in a GMP environment. They will also possess the ability to successfully interface with multidisciplinary teams and build strong cross-functional relationships in a team environment. | 1/31/2023 |
| 5292 | Berkshire Sterile Manufacturing Lee, MA Process Engineering Associate Bachelor’s degree in Chemical Engineering, Chemistry, Biology, or Pharmaceutical Science Exp: one (1) year |
The Process Engineer will lead tech transfer projects from client or small scale to manufacturing/large scale in a manner that meets safety, quality, and operational performance expectations. The key function of this role will be to deliver effective, safe and efficient manufacturing processes for parenteral drug products. | 1/31/2023 |
| 5293 | Biocoat Horsham, PA Chemistry Production Technician Bachelor’s degree in Chemistry or similar science-related field is preferred. Exp: 1 year |
Biocoat is a global leader in manufacturing, applying, and developing hydrophilic coatings for medical devices. Our team needs a Chemistry Production Technician! The technician will perform manufacturing operations for medical device coating products according to Good Manufacturing Practices, ISO requirements, and appropriate regulatory agencies. | 1/31/2023 |
| 5294 | Biomere Richmond, CA Research Associate (Small & Large Animal) AS or BS Degree in Science (or equivalent degree) preferred. Exp: RA I: 1 or 2 years |
Research Associate works under the direct guidance of the Site Head and the general guidance of the senior staff. Research Associate is proficient in animal procedures/animal husbandry, grant, internal, and/or contract research studies according to the study protocols and to the company guidelines and standard operating procedures (SOPs). | 1/31/2023 |
| 5295 | Boston Analytical Salem, NH Analytical Chemist II Bachelor’s degree in Chemistry or a related discipline is required Exp: 1+ years |
The Analytical Chemist II conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. | 2/1/2023 |
| 5296 | Boston Analytical Salem, NH Analytical Chemist I - Nitrosamines Bachelor’s degree in Chemistry or a related science discipline Exp: 0-2 years |
The Analytical Chemist in the nitrosamines laboratory conducts routine screenings of samples for a range of nitrosamine compounds according to FDA, USP, cGMP, and Boston Analytical Inc. Standard Operating Procedures. Duties will include preparation and nitrosamines screening analysis of drug products, APIs, and raw materials using GC-MS and LC-MS. | 2/1/2023 |
| 5297 | Boston Analytical Framingham, MA Microbiologist EM FTE BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The Environmental Monitoring Microbiologist conducts cleanroom monitoring activities to ensure the air, surfaces, and critical utilities utilized for pharmaceutical product manufacturing meet cGMP requirements. These samples are collected according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. | 2/1/2023 |
| 5298 | Boston Analytical Salem, NH Microbiologist - Environmental Monitoring BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The EM Microbiologist conducts quantitative and qualitative analysis of pharmaceutical industries Environment according to FDA, ISO, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include Sampling of pharmaceutical industries through ISO standards and client specific test protocols. | 2/1/2023 |
| 5299 | Boston Institute of Biotechnology Southborough, MA Research Associate / Scientist / Sr. Scientist – Downstream Process Development Bachelor’s degree in Biology or Chemistry related field; MS degree in Biochemistry or Chemical Engineering. Exp: BS: 0-10 years; MS: 0-5 years |
Essential requirements for this position include in-depth understanding and hands-on experience with recombinant protein purification from different expression hosts (including E. coli, Yeast, CHO and HEK) and an aptitude for careful, detail-oriented experimentation. The level of the position will be commensurate with the candidate’s experiences. | 2/1/2023 |
| 5300 | BroadPharm San Diego, CA QC Chemist Bachelor or MS degree in Analytical Chemistry or Organic Chemistry is required Exp: 1-4 years |
BroadPharm is a fast-growing biotech company which specializes in providing high purity PEG products and customer services worldwide. We are seeking a highly motivated QC Chemist to join our expanding team. The ideal candidate would already have 1+ year of working experience with HPLC, MS, and NMR. The position will work closely with the production team and regulatory manager in addition to the current QC staff. | 2/2/2023 |
| 5301 | Cabaletta Bio Philadelphia, PA Associate Scientist/Scientist, MSAT M.S. Exp: 1 + years’ |
The MSAT/Process Development group is seeking a motivated Associate Scientist/Scientist, MSAT who will be responsible for directing cell therapy product candidates through cGMP process development. This position will interact with internal and external partners and require up to 10% domestic travel, as well as occasional weekend and overtime work. | 2/2/2023 |
| 5302 | Bristol-Myers Squibb Redwood City, CA Associate Scientist, In Vivo Pharmacology, Tumor Microenvironment Research Master’s Exp: 0-3+ years |
You will execute in vivo studies, analyze, and present data. You will gain and provide technical and scientific in vivo pharmacology expertise to advance drug discovery programs from target identification/validation to IND enabling activities. You will interact and collaborate effectively in a multi-functional dynamic team environment. | 2/2/2023 |
| 5303 | Bristol-Myers Squibb Devens, MA Associate, QC Microbiology, Cell Therapy Bachelor’s degree required, preferably in the life sciences. Exp: 0-2+ years |
Bristol Myers Squibb is seeking a QC Associate to join our QC Microbiology team at the Cell Therapy Facility (CTF) in Devens, MA. The QC Associate is responsible for supporting Quality Control microbiological in-process, release, and stability testing of clinical and commercial cell therapy drug product. Additionally, the QC Associate will support clean utilities systems testing, environmental monitoring within the manufacturing environment, and may assist with investigations and continuous improvement efforts. The QC Associate role is stationed in Devens, MA and reports to the Manager, QC Microbiology for the Devens CTF. | 2/2/2023 |
| 5304 | Bristol-Myers Squibb Devens, MA QC Associate Microbiology, Cell Therapy Bachelor’s degree required, preferably in the life sciences. Exp: 0-2+ years |
This position offers a $3,500 sign on bonus (external candidates only) The Integrated Genetics Division of LabCorp is seeking a Molecular Technologist to join their Molecular Diagnostics team in Westborough, MA! The Molecular Technologist will be responsible for performing complex molecular testing and results analysis according to established standard operating procedures. The Integrated Genetics-Westborough site processes extracted DNA from peripheral blood and prenatal samples (amniotic fluid and chorionic villi) for genetic testing. A variety of molecular genetics techniques are used to include Next Generation Sequencing, real time PCR, Sanger Sequencing and Southern Blot analysis to test for specific genetic diseases such as cystic fibrosis, spinal muscular atrophy and Fragile X syndrome to name just a few. The schedule for this position will be: Sunday – Thursday (7:00am – 3:30pm) | 2/2/2023 |
| 5305 | Covance Westborough, MA Molecular Laboratory Technologist Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology Exp: 1 year |
LabCorp is seeking a Data Analyst for our Genomics department to join our team of clinical laboratory professionals in Westborough, Massachusetts! The Data Analyst team is responsible for analyzing data generated from clinical molecular laboratories in Research Triangle Park, NC and in Westborough, MA. The team has primary expertise in analyzing sequencing data from next-generation, exome, and Sanger assays, and additional expertise in analyzing copy number data from MLPA and microarray. The team works closely with the laboratory and the clinical directors to ensure high quality results are provided to patients. The schedule for this position is Monday – Friday, 8:30 a.m. – 5:00 p.m. | 2/2/2023 |
| 5306 | Covance Westborough, MA Laboratory Data Analyst (Molecular Genetics) Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology Exp: 1 year |
The successful candidate will work together with our study directors, veterinarians, and quality assurance department to ensure all study aspects are conducted per scientific and regulatory standards. The hands-on experience we offer in the lab has great possibilities for growth with exposure to all aspects of studies including sample preparation, dosing techniques, and surgery, in many different animal models. Highly motivated individuals will have an advancement track through the department. This position is an integral component of a fast-paced environment. The successful candidate will be selected based on aptitude, experience, and a dynamic personality to join our In-Vivo team. | 2/2/2023 |
| 5307 | Covance Bedford, MA Research Assistant Bachelors in a Life Sciences (i.e. biology, pharmacy, veterinary sciences) Exp: 1 year |
We are currently seeking a highly motivated, quality and detail oriented individual to join our In-Vitro Genetox team. The successful candidate will work closely with our study directors and quality assurance to ensure all study aspects are conducted per scientific and regulatory standards. This position is an integral component of a fast-paced environment. You will be joining a rapidly growing team and will be selected based on both experience/aptitude and a dynamic personality. The work is focused on in-vitro testing of medical devices and pharmaceutical products using Good Laboratory Practices (GLP). The main assays performed are AMES, MLA and Chromosomal Aberration testing. Studies are conducted under OECD and ISO guidelines, protocols, and Standard Operating Procedures. | 2/2/2023 |
| 5308 | Covance Saint Paul, MN 2nd Shift, Afternoons- Clinical Technologist Drug Testing Extractions - Wet Chemistry Bachelor's degree from a four?year college or university in chemical, biological or clinical laboratory science or medical technology Exp: 1 year |
The Clinical Toxicology Extraction Technologist Trainee or Technologist receives on‑the‑job training for the pre‑analytical wet chemistry prep of patient samples in the Clinical Toxicology Laboratory. This laboratory is fast‑paced and performs a variety of high complexity testing including therapeutic drug testing, designer panel drug testing, comprehensive oral fluid drug testing, occupational drug testing, autopsy testing, unknown analysis testing, pharmaceutical testing, and drug confirmation testing on blood, serum, urine, and meconium sample types. This testing uses a variety of wet chemistry extraction techniques including liquid-liquid, solid phase, and dilute-n-shoot methods. These extractions utilize both tubes and 96-well plates via manual or semi-automated pipetting systems which are then analyzed on a variety of instrument and software processing platforms. | 2/2/2023 |
| 5309 | Covance Greenfield, IN Research Assistant I Molecular BioA BS, BA, or AS degree in Chemistry, Biology, Biotech, Microbiology, Cellular Biology or related field. Exp: 0-2 years |
Based on continued growth and planned expansion for the CMC (Chemistry Manufacturing & Controls) team, we have multiple openings for Research Assistant I Molecular BioA. This is an entry level position for candidates with 0-2 years of experience, such as recent or upcoming graduates, who are looking to apply their knowledge in a regulatory laboratory environment. Read more about our CMC area https://drugdevelopment.labcorp.com/services/manufacturing-support.htmlBased on continued growth and planned expansion for the CMC (Chemistry Manufacturing & Controls) team, we have multiple openings for Research Assistant I Molecular BioA. This is an entry level position for candidates with 0-2 years of experience, such as recent or upcoming graduates, who are looking to apply their knowledge in a regulatory laboratory environment. Read more about our CMC area https://drugdevelopment.labcorp.com/services/manufacturing-support.html | 2/3/2023 |
| 5310 | Covance Indianapolis, IN Research Assistant I - BioAnalytical Lab Operations Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1- 2 years |
In this position you will be part of a cohesive team and conduct routine analysis on biological and chemical samples in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines for multiple studies. | 2/3/2023 |
| 5311 | Leidos Biomedical Research San Antonio, TX Research Associate I Bachelor’s degree in biology, microbiology or related field Exp: 1+ years |
The Defense Health Operation of Leidos is currently looking for a Research Associate to join the Expeditionary and Trauma Medicine Department supporting biomedical research at the Naval Medical Research Unit, San Antonio (NAMRU-SA) in San Antonio, TX. NAMRU-SA serves as one of the leading research and development laboratories for the U.S. Navy and conducts gap driven combat casualty care, craniofacial, and directed energy research to improve survival, operational readiness, and safety of Department of Defense (DoD) personnel engaged in routine and expeditionary operations. Members of the Expeditionary and Trauma Medicine Department conduct research focused on the protection, resuscitation, and stabilization of combat casualties at front-line points of care in the combat theater. This includes primary and pre-clinical research for the development and optimization of drug products, advanced therapies for the treatment of hemorrhagic shock and identifying and mitigating stressors through the evaluation of products and agents. | 2/3/2023 |
| 5312 | Leidos Biomedical Research Groton, CT Research Assistant - Psychology / Neuroscience / Biomedical Bachelors in psychology, neuroscience, biomedical engineering, or closely related field Exp: 1+ years |
Leidos is currently accepting applications for a full-time, benefits-eligible Research Assistant position, to assist with research studies, research administration, and laboratory management on the Human System Interaction (HSI) Research Team at the Naval Submarine Medical Research Laboratory (NSMRL) onboard Naval Submarine Base New London, located in Groton, CT. The laboratory delivers research solutions promoting the health, welfare, and performance of undersea warfighters. The position is ideal for an individual seeking to deepen their research experience in preparation for graduate study. | 2/3/2023 |
| 5313 | Leidos Biomedical Research Fort Detrick, MD Research Assistant Bachelor of Science in a related discipline. Exp: 1-2 years |
The Defense Health Operation of Leidos is currently looking for a Research Assistant to support biological research at the Biological Defense Research Directorate (BDRD) within the Naval Medical Research Center (NMRC) in Frederick, MD. The BDRD within NMRC facilitates biological research for the rapid detection of infectious diseases of global importance and the enhancement of global disease surveillance for early pathogen detection and response. | 2/3/2023 |
| 5314 | Eli Lilly Indianapolis, IN Biologist - Diabetes, Islet Biology & New Platforms Bachelor’s Degree in biology, molecular biology, biochemistry or related field Exp: 1 year |
The Diabetes, Islet Biology & New Platforms Group is searching for a hardworking scientist at the Associate level with experience in biochemistry and cellular and molecular biology. The successful candidate will work in a multidisciplinary environment and contribute to the discovery and development of novel therapies for Diabetes. The focus of the work will be to identify and validate novel molecular targets for diabetes treatment, and to develop and implement biochemical and cell based in vitro assays supporting drug discovery efforts. The candidate is expected to have a good knowledge base of pharmacology and cell biology and demonstrate willingness to learn new skills. | 2/3/2023 |
| 5315 | Eli Lilly Branchburg, NJ Quality Assurance Associate - Manufacturing Compliance Bachelors degree or higher in the sciences, engineering, or related field Exp: 1-3 years |
The Quality representative provides support to manufacturing and ensures quality systems and GMP compliance. The QA representative provides assistance and guidance in deviation investigations, change control proposals, procedure and master production batch record revisions, validations, and batch dispositions. The QA representative’s position is essential for maintaining quality systems, ensuring GMP compliance and ensuring an inspection readiness state. | 2/3/2023 |
| 5316 | Eli Lilly Branchburg, NJ Research Associate-Quality Control (QC) Bioassay MS in a science related field (e.g. Biology, Biochemistry, etc.). Exp: 1 year |
Conduct routine and non-routine analyses of in-process materials, finished goods and stability samples by appropriate biochemical methods as assigned by supervisor. Perform routine QC responsibilities as needed. Apply acceptable cGMP practices during execution of all work tasks. Work independently with moderate supervisory guidance. | 2/3/2023 |
| 5317 | Eli Lilly Branchburg, NJ Engineer-Reliability BS in Engineering Exp: 1-5 years |
Reliability Engineer is accountable for the equipment reliability and maintenance strategy of the equipment. This is achieved by the continuous monitoring of equipment operational performance and identifying/implementing action needed for improvement. These improvement actions will be a combination of installation set-up, utilization, and maintenance servicing including spare parts, JP/PM, work standardization, etc. Deep understanding of the manufacturing equipment, its processes, and the impact of the processes on the instrumentation/equipment are key to the success of this position. The incumbent will establish many key working relationships to coordinate critical Facilities activities with Quality Control, Quality Assurance, Utility Room, Engineering, and Manufacturing Supervision. Other duties may be assigned at the discretion of the Senior Reliability Engineer. | 2/3/2023 |
| 5318 | Eli Lilly Indianapolis, IN QC Associate - Medical Device Bachelor's degree in STEM discipline Exp: 1 year |
The QC Associate is primarily responsible for assessing, establishing, and supporting quality systems within the Indianapolis Device Manufacturing (IDM) QC organization per applicable Lilly Quality Standards (LQS) and Global Quality Standards (GQS). This role provides daily quality control support, and guidance for the IDM QC Laboratory involving laboratory operations, testing practices, analytical equipment, and test method development impacting the Device Quality Control Laboratory. | 2/3/2023 |
| 5319 | Eli Lilly Indianapolis, IN Engineer - Human Factors MS in Human Factors / Usability Engineering or a related field (e.g., Cognitive Psychology, HCI, Biomedical Engineering, Industrial Engineering, Mecha Exp: 1+ years |
We are seeking an experienced Senior / Principal Human Factors Engineer with an advanced understanding of perceptual, cognitive, and ergonomic theories and principles, and the ability to apply this knowledge to the conceptualization, design, and evaluation of medical devices and digital health systems. The role requires effective collaboration with multidisciplinary team leadership; to work with colleagues from design, engineering, medical, marketing, quality, manufacturing and regulatory to apply human-centered design methods through implementation of usability processes, determination of desired user profiles and environments, development of user documentation, and creation of usability files. | 2/3/2023 |
| 5320 | Alexza Pharmaceuticals Mountain View, CA QC Analyst I/II/III (Temp) Bachelor’s Degree in science or related field Exp: Level I: 0-2 years |
Provide timely analyses to support manufacturing and stability. Primary responsibilities include but not limited to physical testing of components and raw materials, in process and release of commercial product or clinical supplies Independently perform assays under GMP, maintaining data integrity and ensuring compliance with company SOPs and specifications. Provide accurate, written documentation of all work, including detailed observations and conclusions. Under general guidance, participate in laboratory investigations Independently operate, maintain and troubleshoot laboratory instrumentation and equipment in a safe working environment | 1/23/2023 |
| 5321 | Nitto Denko Avecia Cincinnati, OH Quality Assurance Specialist BS/BA in science Exp: 1-3 years |
Acts as departmental resource for cGMP programs, Writes SOP’s compliance documents for cGMP program. Reviews and authorizes batch production records and quality control documentation. Performs compliance audits of suppliers, contract labs and vendors then writes audit reports. Performs internal audits and ensures observations are corrected. Sets-up and tracks material flow and material-labeling process to ensure compliance with cGMP program. Trains staff in area of cGMP and maintains training records. | 1/23/2023 |
| 5322 | Avidity Biosciences San Diego, CA RESEARCH ASSOCIATE B.S./B.A./M.S degree in biological sciences Exp: 1-4 years |
As Avidity advances programs into the clinic, an effective quality control strategy will be critical to ensuring reproducibility of our drug substance. We are seeking a Research Associate to join the Analytics group with experience in mammalian cell biology and/or molecular biology to assist with the development of mammalian cell-based potency assays for late phase drug product release. | 1/23/2023 |
| 5323 | Avidity Biosciences La Jolla, CA RESEARCH ASSOCIATE, IN VIVO PHARMACOLOGY B.S./M.S. in Molecular Biology, Physiology, Pharmacology, or related disciplines Exp: 1-2 years |
We are seeking a highly motivated Research Associate I/II to join our biology team responsible for the preclinical development of drug compounds. Successful candidates will bring hands-on experience in rodent disease models, PD, and PK studies. This is a lab-based position primarily performing, hands-on, in vivo studies in rodents, in vitro work, analyzing data, meeting with key stakeholders to present results, and serving as a team representative. The ideal candidate will be proficient in biological and physiological techniques (in vitro and in vivo), precise documentation, demonstrate clear and professional verbal and written communication, and be a strong team player. | 1/23/2023 |
| 5324 | Avidity Biosciences San Diego, CA SR. RESEARCH ASSOCIATE/ASSOCIATE SCIENTIST B.S./B.A./M.S degree in biological sciences Exp: 1-4 years |
Avidity is seeking an enthusiastic and dedicated Sr. Research Associate/Associate Scientist to join our Discovery Biology team who can assist with ongoing studies that aim to expand our AOC platform. This is a hands-on research position, and a successful candidate will have a proven record of producing exceptional results in a laboratory setting. | 1/23/2023 |
| 5325 | BioRestorative Therapies Melville, NY cGMP Bio -Manufacturing Engineer MSc in cell biology or similar discipline. Exp: 1 to 6 years |
BioRestorative Therapies, Melville, NY is recruiting for a cGMP bio-manufacturing engineer. This role provides outstanding opportunities for talented self-motivated individuals, ideally with experience in (stem) cell biology, immunology, and/or molecular biology, who can contribute to our ongoing efforts to generate clinical grade cell-based therapeutics. We are most interested in connecting with qualified individuals who aspire to support the development of therapeutics and/or life science products and tools to support research endeavors. | 1/23/2023 |
| 5326 | ChemPacific Baltimore, MD Chemist Master’s degree in Chemistry or Organic Chemistry Exp: one year |
Perform multi-step organic synthesis in solution and/or solid support: Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps such as extraction, recrystallization, silica gel column chromatography and LC/MS purification; perform cGMP synthesis of pharmaceutical ingredients; and perform process development and scale-up for kilogram quantities; and clearly record and communicate results and challenges to coworkers/supervisor. Equipments and tolls used included NMR, UV, MS and IR, Reactor (from 50ml to 221 to 10000l), vacuum pump, water aspirator, condenser, rotavap, voltage transformer, chromatography columns, TLC monitor, lyophilizer, separation funnel and addition funnel. Please send your resume to xtan@chempacific.com | 1/24/2023 |
| 5327 | CRISPR Therapeutics Boston, MA Research Associate II, mRNA in vivo MS degree in Chemistry, Chemical Engineering, Analytical Chemistry, Biochemistry, Bioengineering, Pharmaceutical Sciences or related field Exp: 0-3 years |
CRISPR Therapeutics is seeking a highly motivated Research Associate to join our In Vivo Technical Operations department in Boston, Massachusetts. The incumbent will be responsible for the mRNA synthesis and purification optimization to establish process for large-scale mRNA manufacturing. This position will also support therapeutic programs in multiple disease areas in R&D department as well. Prior experience in mRNA synthesis, purification and characterization is desired. | 1/24/2023 |
| 5328 | CRISPR Therapeutics Boston, MA Research Associate II/Senior Research Associate, Toxicology RA II: MS in biology or related disciple Exp: 0‒2 years |
We are seeking a Research Associate II/Senior Research Associate to build our capabilities within our In Vivo Pharmacology team. The successful candidate will be responsible for implementation of in vivo studies involving mice and rats. The candidate should be proficient handling, administering test article, and sample collection from both species. The candidate will work on all aspects of implementing in vivo studies: design, administration, in-life observations, postmortem analysis, report generation, and data presentation. The In Vivo Pharmacology team interacts with most of the research groups within CRISPR, offering the candidate exposure to a variety of different programs and platforms. | 1/25/2023 |
| 5329 | NorTech Life Sciences Blue Earth, MN Project Engineer Bachelor's degree (BS) from four-year college or university Exp: 0+ years |
Introduce new products into manufacturing and service. Determines engineering and design requirements; resolves engineering problems; verifies and maintains project time lines; meets cost standards; evaluates manufacturing systems applications; confirms systems and components capabilities; develops manufacturing processes and standards; assures product quality; prepares technical product reports. May develops manufacturing methods, systems and processes to produce a high-quality product at optimal cost for new product introduction. | 1/25/2023 |
| 5330 | Physical Sciences Boston, MA CHEMICAL ENGINEER BS or MS degree in Chemical Engineering, Chemistry or Materials Science Exp: 0 to 2 years’ |
Physical Sciences Inc., located just north of Boston, in Andover, is seeking a Chemical Engineer with a strong background in reaction kinetics, heat and mass transfer, and separations. We are seeking an applicant who can assist with developing and scaling-up materials production from laboratory/batch processes to pilot-scale/continuous processes. The applicant we seek would ideally have materials synthesis, purification and characterization experience. We are looking for a strong worker, who can safely and effectively execute on their ideas as a member of a team and sometimes as an individual contributor. This individual will play a key role in growing a diverse portfolio of technologies funded by the DoD, DoE, and NASA, in areas such as firefighter decontamination, atmospheric water harvesting and microreactor technology development. | 1/25/2023 |
| 5331 | Physical Sciences Boston, MA CHEMICAL ENGINEER/CHEMIST Bachelors or Masters in Chemistry, Chemical Engineering, Physics, Applied Physics, Material Science or related field is required. Exp: Entry-level |
Physical Sciences Inc., located just north of Boston in Andover, seeks well-qualified candidates for positions on our research and manufacturing team. This position is intended for an individual who is interested in supporting and leading programs devoted to the development and manufacturing of products that employ active photonic materials. An ideal candidate should be interested in a career devoted to applied research and product development with strong experimental, hardware, and leadership skills, and should be interested in maturing technologies and manufacturing processes from concept to prototype. | 1/25/2023 |
| 5332 | Tanvex BioPharma San Diego, CA QC Associate, Lab Control & Raw Material - #1346 Bachelor’s degree or advanced degree in chemistry, biology, biochemistry or related life sciences discipline. Exp: 0-3 years’ |
The Quality Control Associate, Lab Control & Raw Materials is responsible for conducting routine and non-routine analyses of raw material and GMP product as assigned using appropriate analytical methods. This position will coordinate sampling, shipping, and testing of raw materials at outside contract laboratory and in-house to ensure data integrity and compliance, and will work with internal departments to ensure timely testing of raw materials for Manufacturing. | 1/26/2023 |
| 5333 | Tanvex BioPharma San Diego, CA Research Associate, Cell Culture Process Development - #1358 BS or advanced degree in chemical/biochemical engineering, cell biology, biochemistry, or related scientific discipline. Exp: 0-3 years |
The Research Associate, Cell Culture Development is responsible for executing individual experiments related to all aspects of cell culture process development of biopharmaceuticals, including media preparation, bioreactor setup, cleaning, sterility and operation, maintaining instruments and equipment, examining data and preparing experiment reports. Applies basic engineering and scientific principles to perform trouble-shooting of processes, instrumentation, and equipment. | 1/26/2023 |
| 5334 | Tanvex BioPharma San Diego, CA Research Associate, Bioassay Development - #1438 BS or advanced degree in cell and/or molecular biology, or related scientific discipline. Exp: 0-3 years |
The Research Associate, Bioassay Development is responsible for biological characterization of Biologics drug candidates including method development, method qualifications, method transfer and training, and routine non-GMP sample testing. Designs, executes and documents a set of experiments that contribute to project objectives. | 1/26/2023 |
| 5335 | Tanvex BioPharma San Diego, CA Manufacturing Associate, Downstream Bachelor's or advanced degree in life sciences or related discipline Exp: 0-3 years |
Under general supervision, the Manufacturing Associate, Downstream, will perform routine manufacturing activities in GMP manufacturing areas including purification and the associated sub-processes/ preparation. Operations will be performed according to Standard Operating Procedures (SOPs) and batch records. Perform manufacturing steps, execute routine batch records, and revise documents such as batch records and SOPs as needed. Flexible shift schedules and overtime may be required. | 1/26/2023 |
| 5336 | Tanvex BioPharma San Diego, CA Research Associate, Analytical Chemistry Development BS or advanced degree in chemical/biochemical engineering, biochemistry, or related scientific discipline. Exp: 0-3 years |
The Research Associate, Analytical Chemistry Development is responsible for providing analytical chemistry support to research, process development, product development and manufacturing of biological therapeutics. Participate in analytical method development, characterization, qualification, validation as well as method transfer. Perform various analysis for characterization of biological therapeutics. | 1/26/2023 |
| 5337 | UniQure Lexington, MA QA Specialist I Bachelor’s degree in Life Sciences or Engineering Exp: 1-3 years |
The Quality Assurance Specialist I supports the day-to-day quality operations via Manufacturing Clean Room presence, Material/Inventory QA Release, oversight of all elements of the Quality Management System (QMS), including but not limited to deviations, Corrective and Preventive Actions (CAPAs), investigations, change control, batch review, data integrity, and training in support of biologics manufacturing production. | 1/26/2023 |
| 5338 | UniQure Lexington, MA QC Analyst BA or BS in Chemistry/Biology or other related science Exp: 1-6 years |
The QC Analyst will be responsible for GMP routine/nonroutine QC testing of our AAV-based products and the raw materials/starting materials used according to SOPs. This position supports the second shift at uniQure’s state of the art facility in Lexington, MA. | 1/26/2023 |
| 5339 | Advanced BioScience Labs Rockville, MD QC Microbiology I - (00325_COMPANY_1.5) Bachelor’s degree Exp: 1-2 years’ |
The Quality Control Microbiologist will have several responsibilities in the Quality Control Group. The Analyst will perform environmental monitoring (EM) for particulates and viable samples in support of cGMP manufacturing. This includes several production suites of EU Grade A to D in a GMP facility that produce biopharmaceuticals (vaccines, biologics, viral vaccines, monoclonal antibodies, etc.) In addition, monitoring of purified water, and compressed gases systems is required. Additional responsibilities may include EM data review and compilation and verification of data, report writing and trending of data, gowning training and annual gowning qualification. | 1/26/2023 |
| 5340 | Abenza Bristol, PA Associate II – Quality Control Sample Coordinator Bachelor’s degree in Scientific discipline Exp: 1+ years |
The QC Sample Coordinator Associate II performs incoming and outgoing sample management for in process, release and stability studies. This role is also responsible for reference standard inventory and reconciliation to support all laboratory testing. Complies with policies and procedures in order to maintain compliance with legal regulations, health and safety, and regulatory requirements. Ensure samples are delivered in line with organizational standards, protocol specific requirements and client expectations. Travel between Abzena sites (Bristol PA, San Diego CA and Sanford NC) as needed. | 1/26/2023 |
| 5341 | Advanced Cell Diagnostics Austin, TX Research Associate Bachelor’s degree in biology, chemistry, biomedical engineering, or related field is required. Exp: 1-3 years |
Asuragen is seeking an outstanding BSc-level scientist to join our Research group. This is a full time position focused on developing innovative nucleic acid or protein-based technologies. This role will support new product initiatives to enable novel, multiplexed-PCR technologies that can resolve multiple classes of DNA/RNA markers or proteomics through integration of reagents, instrumentation, analysis algorithms and software. Platforms used in our laboratory include quantitative real-time PCR, digital PCR, capillary electrophoresis, next-generation and long-range sequencing. | 1/27/2023 |
| 5342 | Adesis Wilmington, DE Purification Chemist Bachelor of Science in Chemistry or other relevant field Exp: 1-2 year |
Responsible for assisting chemists in performing various purifications of target compounds in a fast-paced research environment. Purification techniques include, but are not limited to preparative high performance liquid chromatography (prep HPLC), normal phase and reverse phase chromatography, and recrystallization. | 1/27/2023 |
| 5343 | Agenus Lexington, MA Associate Scientist/Scientist I, Analytical Sciences, Mass Spectrometry Master in analytical chemistry Exp: 1-3 years |
An enthusiastic Associate Scientist / Scientist I, ideally with large/complex and small biomolecule analytics expertise in Mass Spectrometry, to join our Mass Spectrometry team as a potential subject matter expert with the goal to oversee and support the characterizations of Agenus therapeutic protein pipeline at various stages. | 1/27/2023 |
| 5344 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Manufacturing Associate I Bachelors in a science or engineering discipline preferred. Exp: zero to two (2) years |
We are currently seeking a Drug Manufacturing Associate I who is responsible for executing GMP production of injectable pharmaceuticals by following all applicable SOP's. Manufacturing associates are responsible for preparing equipment and materials for GMP aseptic production and operating equipment such from glasswashers, autoclaves, depyrogenation ovens and automated filling machines. | 1/27/2023 |
| 5345 | Ajinomoto Bio-Pharma Services San Diego, CA Lab Systems Analyst Bachelor’s degree preferred in a Life Sciences discipline, IT, or equivalent preferred. Exp: 0-2 years |
We are currently seeking a Lab System Analyst to support lab systems for Analytical Technologies and Quality Control at Ajinomoto Bio-Pharma Services. This includes supporting one or more of the following: Benchtop lab equipment and computers, LIMS, ELN, MODA, CPMS, chromatography data system (CDS), equipment life cycle management, and data integrity. The Lab Systems Analyst may also perform routine maintenance and repair of the quality lab systems according to standard operating procedures. | 1/27/2023 |
| 5346 | Ajinomoto Bio-Pharma Services San Diego, CA Manufacturing Associate I Formulations 2nd Shift Bachelor’s degree in a Life Sciences discipline or equivalent preferred. Exp: Zero to two (0-2) years |
We are currently seeking a Drug Product Formulations Manufacturing Associate I who is responsible for execution of routine production and manufacturing procedures to support processes and ensure compliance with regulatory requirements. The Manufacturing Associate I will work with the Drug Product team to ensure the successful completion of various cGMP activities. The Manufacturing Associate I will learn and demonstrate proficiency in both the technical aspects as well as the quality systems which govern cGMP manufacturing. | 1/27/2023 |
| 5347 | Ajinomoto Bio-Pharma Services San Diego, CA Microbiology Technician - 1st Shift Bachelors degree preferred in a Life Sciences discipline or equivalent. Exp: Zero to two (0-2) years |
We are currently seeking an Microbiology Technician to support Ajinomoto Bio-Pharma Services manufacturing. This is a vital role within our Quality Control group and is responsible for supporting manufacturing through collection and testing of water, surface and utility samples during various manufacturing and lab processes. As an Environmental Monitoring Assistant you will acquire an understanding of aseptic technique, continuously exhibit proper clean room behavior, and adhere to cGMPs. | 1/27/2023 |
| 5348 | Ajinomoto Bio-Pharma Services San Diego, CA Microbiology Technician - 2nd Shift Bachelor’s degree preferred in a Life Sciences discipline or equivalent. Exp: Zero to two (0-2) years |
Microbiology Technician – 2nd shift will support Ajinomoto Bio-Pharma Services manufacturing. This is a vital role within our Quality Control group and is responsible for supporting manufacturing through collection and testing of water, surface and utility samples during various manufacturing and lab processes. You will acquire an understanding of aseptic technique, continuously exhibit proper clean room behavior, and adhere to cGMPs. | 1/27/2023 |
| 5349 | American Regent New Albany, NY R&D Associate Scientist 1- Formulation Development B.S. in Pharmaceutical Science, Chemistry, Chemical Engineering or equivalent required. Exp: B.S.: 0-3 years; M.S.: 0-1 year |
Responsible for formulation and process development activities associated with parenteral drug product development. Participates in scale-up of manufacturing process. | 1/27/2023 |
| 5350 | Ampac Analytical Rancho Cordova, CA Process Engineer Bachelor's of Science Degree in Chemical Engineering required. Exp: One to three years |
We are looking for enthusiastic Chemical Engineers to join our Process Engineering Team! We have several opportunities at our Rancho Cordova, CA location (Greater Sacramento Area). We will pay for your relocation!! | 1/27/2023 |
| 5351 | Ampac Analytical Rancho Cordova, CA Technical Operations Lead I bachelor's degree Exp: 0-1 years |
The position provides continuous technical support and guidance for plant operations. This role provides rapid technical response to issues employing manufacturing techniques to solve problems. This position must have a good understanding of production priorities and will direct production activities accordingly to maximize labor efficiency. This role is responsible for daily activities of production area to ensure that volume, cost, and quality standards are achieved. Work is moderately supervised. Follows specific, detailed instructions. | 1/27/2023 |
| 5352 | Ampac Analytical Rancho Cordova, CA Quality Chemist I Bachelor’s degree in Chemistry or an appropriate science required. Exp: One (1) to two (2) years |
We are looking for enthusiastic Chemists to join our QC Team in Rancho Cordova (Greater Sacramento area)! | 1/27/2023 |
| 5353 | Ansa Biotechnologies Emeryville, CA Manufacturing Associate, Protein Downstream Process Bachelor’s/Master’s Exp: 0-2 years |
Implementing a robust protein production pipeline will be instrumental in providing the key reagents needed to implement the fastest, cleanest, and most accurate DNA synthesis system in the world. As a Manufacturing Associate in the Protein Production team, you will have the exciting opportunity to transition our protein production from research to pilot scale and beyond. You’ll have the exciting opportunity to learn the ins and outs of research and pilot scale recombinant protein purification. | 1/27/2023 |
| 5354 | Arbor Biotechnologies Cambridge, MA Research Associate, CRISPR Early Discovery Bachelor’s degree in biology, biochemistry, molecular biology, or a related field Exp: 1-3 years |
Arbor Biotechnologies is seeking a Research Associate to join our CRISPR Early Discovery team to aid in the earliest stages of discovery and characterization of new gene editing systems. The ideal candidate will have an appetite for learning a wide variety of topics, is self-motivated, and thinks critically about experimental design. | 1/27/2023 |
| 5355 | Arbor Biotechnologies Cambridge, MA Research Associate/Senior Research Associate, Non-Viral Gene Therapy BS/MS or equivalent in Chemical/Biomedical/Biochemical Engineering, Bioengineering, Chemistry, Biochemistry, Pharmaceutical Sciences or a related fiel Exp: 1-3 years |
The Senior Research Associate/Research Associate will support our LNP formulation pipelines and in vitro/in vivo preclinical requirements through the design and execution of experiments to help screen and produce various non-viral formulations enabling the encapsulation of various RNA entities. This candidate will also support various biophysical characterization assays commonly used in nanomedicine. The ideal candidate for this position will be a motivated and proactive individual with a passion for LNP and other nanoparticle formulations and processes. The applicant should have strong wet laboratory, communication and collaboration skills preferably with a background in the appropriate formulation deliverables. This role will have no supervisory responsibilities and will report to the Principal Scientist, Non-Viral Gene Therapy. | 1/27/2023 |
| 5356 | Arbor Biosciences Ann Arbor, MI Lab Technician, NGS team Bachelor’s degree involving molecular biology laboratory work and /or relevant work experience Exp: 6+ months |
This is a role for a talented molecular biologist with experience working with DNA and RNA to perform laboratory experiments as part of our client service offerings. The Laboratory Technician will have project management responsibilities and will be adept at molecular biological bench work. Routine activities will involve standard NGS techniques. Research & development activities using the same skills are possible. Fundamental understanding of the concepts and methods of PCR, ligation and other enzymatic reactions, strong laboratory skills, organizational skills, note-taking diligence and attention to detail are key. | 1/27/2023 |
| 5357 | Arcturus Therapeutics San Diego, CA Research Associate, Analytical Development Bachelor’s degree in Chemistry, Biochemistry, Molecular Biology, Pharmaceutical, Life Science or equivalent. Exp: Zero to two (0-2) years |
The Research Associate, Analytical Development will be responsible for conducting routine analytical characterization of RNA drug substances, intermediates and formulated drug products to support an emerging research pipeline focused on treating rare diseases. The candidate will also assist with optimization, development and implementation of new analytical procedures as needed. | 1/27/2023 |
| 5358 | Arcturus Therapeutics San Diego, CA Research Associate / Senior Research Associate, Frontier Science Bachelor’s or Master’s Degree in Cellular Biology, Molecular Biology, Biochemistry, or a related field. Exp: 0-3 years |
The Research Associate I/I, Frontier Science will conduct hands-on experiments in the Frontier Science department with a wide variety of cellular biology, molecular biology, and biochemistry techniques. This person will be expected to complete scientific and technical tasks on aggressive timelines and to work as part of a team on varied projects with changing priorities. This position requires excellent communication skills, an outstanding ability to troubleshoot technical issues, a superior ability to plan and carry out experiments independently, and to work with complex instrumentation and software. Exact title and responsibilities will be commensurate with experience. | 1/27/2023 |
| 5359 | Ascendis Pharma Redwood City, CA Research Associate, Analytical Development - CONTRACT Bachelors/Masters degree in chemistry, chemical engineering, biochemistry, or a related field Exp: 0-4 yrs |
The Research Associate will be responsible for conducting laboratory-based analytical development activities to support Ascendis Pharma’s growing pipeline of pre-clinical and clinical programs. Working closely with a team of scientists and engineers in our brand new Redwood Shores laboratory, the Associate Scientist will characterize complex small molecule-based compounds to support process, formulation, and analytical development activities. This position offers great potential for growth of scientific and drug development experience while working on exciting, complex, and impactful products. | 1/27/2023 |
| 5360 | United Therapeutics RTP, NC Research Associate I/II - Analytical Development Bachelor’s degree in arts/sciences (BA/BS) in biology, cell or molecular biology or biomedical sciences Exp: RA I: 1+ years |
Conduct and assist in analytical efforts to evaluate tissue, cell, and cell-secreted products for treating lung disease. | 1/16/2023 |
| 5361 | United Therapeutics Manchester, NH Research Associate I/Research Associate II, Analytical Development, Cell Production Bachelor’s Degree in Arts/Sciences (BA/BS) in cellular biology, developmental biology, biomedical engineering or related field Exp: RA I: 1+ years |
The Research Associate II – Analytical Development will develop and execute analytical methods to support the production of iPS-derived cells and cellularized 3D scaffolds for the development of autologous 3D printed tissue engineered organs. | 1/16/2023 |
| 5362 | United Therapeutics Manchester, NH Associate Process Engineer/ Process Engineer, Biomaterials Bachelor’s Degree in Arts/Sciences (BA/BS) in materials science, chemistry, chemical, mechanical or biomedical engineering (or equivalent) Exp: 1+ years |
The Associate Process Engineer, Biomaterials (OMG) will be responsible for scaling up and experimenting with large batches of ink to support process and product feasibility goals. This position will also be responsible for periodic quality control (QC) testing. | 1/16/2023 |
| 5363 | United Therapeutics RTP, NC Bioprocess Associate I/II - Cell Biology, Bioprocess Development Bachelor’s Degree in Arts/Sciences (BA/BS) in biology, cell and molecular biology, biomedical sciences, biomedical engineering, biomanufacturing, or a Exp: Bioprocess Associate I: 1+ years |
Conduct and assist in research efforts to develop tissue-based regenerative medicine products for the treatment of pulmonary hypertension and other lung diseases. | 1/16/2023 |
| 5364 | United Therapeutics Manchester, NH Research Associate I – Cellularization Bachelor’s Degree in Arts/Sciences (BA/BS) in Cellular Biology, Developmental Biology, or Biomedical Engineering or related field Exp: 1+ years |
The Research Associate I - Cellularization (OMG) will support the development and characterization of bioinks for 3D printing scaffolds for lung tissue engineering. They will design and print 3D diagnostic models to test bionks for compatibility with different lung cell types. | 1/16/2023 |
| 5365 | UPM Pharmaceuticals Bristol, TN Microbiologist 1 Bachelor’s Degree in Microbiology or related science field Exp: 0-2 years |
Learns to and performs routine microbiological quality control testing of pharmaceutical products and related materials in accordance with site policies, departmental procedures, compendial methods and cGMP regulations. Participates in programs to achieve departmental objectives; records and reports results; notes unusual results and notifies supervision for evaluation. | 1/16/2023 |
| 5366 | Upsher-Smith Maple Grove, MN Analyst - QC Bachelor's Degree in Chemistry or related science field Exp: 0 years |
Provides analytical and technical support for analysis of raw materials (drug substances, excipients, in-process samples, and packaging components) stability samples, and drug products. Completes testing in a timely manner according to cGMPs, test methods, and SOPs. Works with dissolution, ion chromatography, pH meters, karl fisher titrations, balances, and various other auxiliary laboratory equipment. | 1/18/2023 |
| 5367 | Vericel Cambridge, MA Technician, Cell Therapy Manufacturing Biotechnology certificate or equivalent Exp: 0-2 years |
Responsible for the execution of process steps to manufacture commercial cell therapy products meeting internal and regulatory requirements. | 1/18/2023 |
| 5368 | Veracyte San Diego, CA Clinical Lab Technician Bachelor’s degree Exp: 1 years |
The Clinical Lab Technician’s primary responsibility is to provide front-line support in the procurement of record of loan (ROL) material and manage chain-of-custody of samples received. This individual must support the Decipher internal and external customers in the routine functions to ensure client satisfaction and appropriate records and materials management are consistently maintained. This individual must work with staff to employ a team approach. Manages patient orders with or without samples and oversees special projects assigned by their supervisor. The schedule for this role will be Tuesday - Saturday. | 1/18/2023 |
| 5369 | Verge Genomics South San Francisco, CA In Vitro Senior Research Associate I/II MS in biochemistry, biology or related field Exp: 0-2 years |
Screen compounds in model systems, including successful replication of results in duplicate and triplicate studies Independently plan and perform in-vitro assay and techiques in support of high throughput and medium throughput projects. Directly screen compounds in various in-vitro models including biochemical/ biophysical and mammailan cell culture assays. Review and write SOPs and project research plans | 1/18/2023 |
| 5370 | Vor Biopharma Cambridge, MA Associate Scientist/Senior Associate Scientist, Discovery & Molecular Engineering Bachelor’s or master’s degree in molecular biology, biochemistry, genetics, or a related discipline is required Exp: BS: 0-2+ years’; MS:1+ years |
Vor Bio is seeking an Associate/Senior Associate Scientist, in the Discovery & Molecular Engineering department/team. The candidate will contribute to advancing next-generation editing, including base editing, and characterization approaches towards developing Vor’s genome-engineered hematopoietic stem cell as well as immuno-oncology products. The candidate will work within a team environment to execute experimental plans in cell engineering development within the Discovery & Molecular Engineering team at Vor. | 1/18/2023 |
| 5371 | Voyager Therapeutics Cambridge, MA Research Associate/Sr. Research Associate, Histology For RA, MS Exp: 1+ years |
Reporting to the Senior Scientist, the Research Associate OR Senior Research Associate will contribute to Voyager’s research team at its facility in Cambridge, Massachusetts. This is a hands-on position for a person committed to helping the broader team conduct innovative drug discovery research in a collaborative environment. We are seeking a person who is enthusiastic about biomedical research and can work in close partnership with other scientists and team members. This is an ideal position for an individual with extensive experience in immunohistochemistry (IHC), immunofluorescence (IF), and in-situ hybridization (ISH) assay development. The ideal candidate will demonstrate thorough knowledge of experimental design and independent thinking to support multiple programs. The RA or S. RA must be a highly motivated individual with the ability to oversee project timelines and deliverables and interpret and communicate results. | 1/19/2023 |
| 5372 | ZeptoMetrix North Charleston, SC Chemist, QC I Bachelor's degree in Chemistry or related field. Exp: 1 year |
The Quality Control (QC) Chemist is primarily responsible for the quality control of starting materials, in-process materials and the finished goods. The incumbent must be a dynamic individual who can work in a diversified group and able to handle multi-tasks within QC operations. The candidate must possess a good working knowledge of Analytical Chemistry. This position requires hands on chemistry lab work and troubleshoot instruments and solve complex spectroscopic problems. | 1/19/2023 |
| 5373 | ZeptoMetrix North Charleston, SC Chemist I Bachelor’s degree in Chemistry, Engineering or related field Exp: Up to 2 years |
The Chemist I will involve all manufacturing tasks related to the production of the company’s inorganic products. Responsibilities include manufacturing, handling and packaging of concentrates and single/multi-element reference solutions as per standard operating procedures. The incumbent must be a dynamic individual who can multi-task and perform various activities associated with manufacturing operations while adhering to all safety policies and high quality Standard Operating Procedures. This position requires hands on chemistry lab work and will report to the Inorganic Production Manager. | 1/19/2023 |
| 5374 | Zimmer Biomet Warsaw, IN Technician (718246) College/University courses in Microbiology, Biology, Chemistry, Engineering Mechanics, Medical Technology or other related field preferred. Exp: 0 – 3 years |
Responsible for supporting the daily operations of the laboratory at all Zimmer Biomet Warsaw facilities and for operating and maintaining laboratory equipment for the necessary assigned tasks per area work instructions. May also be responsible for ensuring that equipment calibration and maintenance (preventive and/or corrective) is performed. | 1/19/2023 |
| 5375 | Zimmer Biomet Warsaw, IN Manufacturing Engineer (723066) S. in engineering Exp: 0-3 years |
The manufacturing engineer is responsible for providing manufacturing engineering services to support efficient manufacturing processes. Engineering services may include cell management, process development, project management, process validation, tool design, and trouble shooting. | 1/20/2023 |
| 5376 | Zimmer Biomet Olive Branch, MS Quality Engineer (722350) B.S. in engineering or an alternative Bachelor’s degree program with certification as a quality engineer (e.g. CQE). Exp: 0-3 years |
Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. Interacts with many different functional departments, suppliers, and experts outside Zimmer Biomet to implement Zimmer Biomet Quality goals. | 1/20/2023 |
| 5377 | Zogenix Cambridge, MA Research Associate I/II - Translational Biology BA/BS or MS Degree in biology, cellular biology, bioengineering or related field Exp: 0-2 years |
We are seeking a Research Associate I/II to join the translational biology group and contribute to translational biology drug discovery efforts. The candidate will be responsible for characterizing and deploying stem cell/3D models and other cellular/biochemical assays to be utilized in early drug discovery for multiple therapeutic programs. He/She will also collaborate in a matrixed team of scientists responsible for identification and knowledge building across pathobiological pathways and patient populations including those in neurology, neuromuscular disease and diseases caused by nucleotide repeat expansions. | 1/20/2023 |
| 5378 | Zogenix Cambridge, MA Senior Research Associate / Biology Protein Sciences BA/BS or MS Degree in biology, biochemistry, chemical biology, protein engineering or related field Exp: RA: 0-2 years |
As a (Senior) Research Associate you will contribute to drug discovery efforts for multiple therapeutic areas including neurology and immunology. You will divide your time between our groups to conduct recombinant protein expression and macrocycle screening for therapeutic programs. This is an exciting opportunity to gain experience in multiple technical areas. | 1/20/2023 |
| 5379 | Accelerate Diagnostics Tucson, AZ Research Associate, Quality Control Bachelor of Science degree in Microbiology, Biochemistry, Molecular Biology, Chemistry, or related life sciences. Exp: 1 year |
The Research Associate for Quality Control is a key member of the Operations Team under the direction of the Team Lead for Consumable Quality Control. This individual will be responsible for testing of incoming product both analytically and biologically in support of manufacturing. This will include, but not limited to, operation of pH/conductivity meter, refractometer and in-house biotechnology systems. This person will be part of a team that executes these tasks on a daily basis. The ideal candidate will be a team player, demonstrate excellent communication skills, be flexible, and excel in a fast-paced environment. | 1/20/2023 |
| 5380 | Accurus Biosciences Richmond, CA Research Associate Bachelor’s or Master’s degree in Biology Exp: 0-3 years |
The successful candidate will perform a range of duty critical to our research service business. The primary responsibility of this position is general molecular biology which includes DNA cloning, site directed gene mutagenesis, plasmid DNA preparation and DNA restriction analysis. Additional responsibilities for this position may include mammalian cell culture, protein transient production, stable cell line generation and general lab maintenance. | 1/20/2023 |
| 5381 | Affinivax Cambridge, MA USP Associate Scientist, Carrier Unit BS/MS in related fields such as Chemical Engineering, Bioengineering, Biochemistry, or Biology Exp: 0-2 years |
Within the Carrier Unit group, you will integrate with a multidisciplinary team in charge of fermentation and purification of recombinant proteins and polysaccharides. You will be in close contact with experts in upstream, downstream and various analytical technologies. Your mission will be focused on the development and execution of upstream processes in different research and development contexts (early development, processability, process development, process understanding, troubleshooting, Life cycle…)The successful candidate will report to the manager of Carrier Unit, which is part of the Microbial Drug Substance organization in Technical R&D (TRD). | 1/20/2023 |
| 5382 | Affinivax Rockville; Boston, MD Associate Scientist Bachelor's degree (biotechnology, molecular biology, biochemistry, molecular, bacteriology, molecular, microbiology). Exp: One or more years |
As Associate Scientist within the Molecular Analytics platform, you will be in charge of implementing, designing and developing methods for the detection and quantification of nucleic acids based on up-todate nucleic acid technologies (NAT) and, in particular, methods aiming at characterizing plasmids (topology, conformation, sequence, quantity, etc.), mRNA Drug Substances (content, integrity, identity) and mRNA-LNP Drug products (monovalent and multivalent), used for production of mRNA vaccines. The use of direct nucleic acid quantification methods (e.g. CRISPR-based assays, digital counting through optical barcodes, branched DNA assays, etc.) will part of the activities of the hired Scientist. | 1/20/2023 |
| 5383 | Affinivax Cambridge, MA Associate Scientist, MAPS Analytical GMP Testing Bachelor/Master of Science in Biology, Molecular Biology, Biochemistry, Chemistry, Analytical Chemistry Exp: 1+ years |
Leveraging our highly innovative Multiple Antigen Presenting System (MAPS) platform technology, we are pioneering the development of a novel class of vaccine. To support this, we have a number of newly created opportunities for Associate Scientists to join our Quality Control Team to support and contribute to our development efforts and ongoing clinical trial. | 1/20/2023 |
| 5384 | Aytu BioScience Grand Prairie, TX Chemist I Bachelor's degree in a science-related field or equivalent experience Exp: 1 year |
The QC Chemist I position plays a key role in the operation of the QC Laboratory. This chemist will be responsible for the timely analysis of a wide variety of samples. The QC Chemist I provide services for other departments (Production, R&D, QA, Engineering), all while operating in a state of compliance with current Good Manufacturing Practices (cGMPs). | 1/20/2023 |
| 5385 | Carmot Therapeutics Berkeley, CA Research Associate I/II, Biology BS or MS in cellular biology, biochemistry, molecular biology or related field Exp: 1-4 years |
As a Research Associate in the Biology group, you will contribute to discovery efforts to identify new drug candidates by generating high-quality screening data using a variety of plate-based cellular and biochemical assays. Additionally, you will help develop new methods to interrogate compound mechanism of action, effect on cell signaling and physiology. This position requires working closely with scientists in biology, pharmacology, and chemistry as part of a multidisciplinary team in a fast-paced environment. At Carmot we value diverse perspectives and encourage our employees to contribute at multiple levels within the company, including strategic development. | 1/20/2023 |
| 5386 | EpiVax Providence, RI Research Associate I Bachelor of Science in Immunology, Biomedical Engineering or Biotechnology is required. Exp: 1-3 years |
The Research Associate I will be responsible for executing scientific research in the laboratory specifically related to the development of vaccines and therapeutic proteins, in addition to maintenance of general laboratory functions. The Research Associate I will be responsible for executing scientific research in the laboratory specifically related to the development of vaccines and therapeutic proteins, in addition to maintenance of general laboratory functions. | 1/20/2023 |
| 5387 | Sciecure Pharma Monmouth Junction, NJ QC & ARD Chemist Bachelor’s degree from four-year college or university in any of the following disciplines: Chemistry, Biology, Microbiology, or related sciences (as Exp: 1 year |
The Analytical R&D laboratory supports, development and validation of methods analytical test methods, evaluation and testing of raw materials, and testing of non-commercial materials to support product development. All activities are performed in accordance with specifications, standard operating procedures, approved test methods and/or protocols, regulatory requirements. | 1/20/2023 |
| 5388 | SparX Therapeutics Mount Prospect, IL Associate Scientist MS degree in biochemistry, molecular biology, or related discipline. Exp: 0-2 years |
SparX is seeking a highly motivated and enthusiastic Associate Scientist in protein expression, purification and characterization. The role will involve cell culture, plasmid preparation, protein expression and purification using a variety of cell culture systems, protein characterization, and evaluation. | 1/20/2023 |
| 5389 | SparX Therapeutics Mount Prospect, IL Associate Scientist Phage Display MS degree in biochemistry, molecular biology, or related discipline. Exp: 0-2 years |
SparX is seeking a highly motivated and enthusiastic Associate Scientist in antibody engineering through high-throughput screening. Experience in phage display is strongly recommended. The role will involve basic molecular cloning, antibody library construction and screening. Knowledge in antibody humanization and affinity maturation is a plus. | 1/20/2023 |
| 5390 | SparX Therapeutics Mount Prospect, IL Research Associate, In Vitro Pharmacology Master’s degree in cell biology, oncology, immunology or related field. Exp: 1+ years |
Position Summary: SparX is looking for a highly motivated, interactive and creative Research Scientist with a strong cell biology background to join the pharmacology team. The primary responsibilities of the Research Associate will be to develop and perform in vitro cellular and/or biochemical assays for antibody drug candidates screening, biological function evaluation in immuno-oncology and oncology drug discovery program. | 1/20/2023 |
| 5391 | SparX Therapeutics Mount Prospect, IL Associate Scientist Cell Culture MS degree in cell biology or related discipline. Exp: 0-2 years |
SparX is seeking a highly motivated and enthusiastic Associate Scientist in Cell Culture. Experience in mammalian cell culture is required. | 1/20/2023 |
| 5392 | Spriaso Salt Lake City, UT Research Chemists Bachelor's degree in chemistry, chemical engineering, biochemistry, or other related degree concentration. Exp: one year |
These positions entails doing product, process, and analytical functions in support of product and technology development under direction of product development and/or analytical leader. | 1/20/2023 |
| 5393 | Aesculap Irvine, CA Microbiologist I Bachelor's degree required. Exp: 0-02 years |
Plans, coordinates and organizes the overall activities of the Microbiological Laboratory according to internal and external standards in a most cost effective way. Directly responsible for the supervision test operation at all time for Sterility Testing, Bacterial Endotoxin Test, Microbiological Identification Sections and handling of laboratory OOS result. Ensures that the necessary microbiological tests are done according to the test specification, test method and working instruction and to ensure release on time for pharmaceutical products and medical devices. | 1/20/2023 |
| 5394 | Aesculap Irvine, CA QC Microbiology Associate II (Micro Product Testing Lab) Bachelor's degree in a Science related field preferred. Exp: 01-02 years |
Performs routine functions and analysis (dependent upon experience) as required by the specific laboratory requirement in compliance with B. Braun and cGMP specifications. | 1/20/2023 |
| 5395 | Aesculap Irvine, CA QC Microbiology Associate II (Sterility Media) Bachelor's degree in a Science related field preferred. Exp: 01-02 years |
Performs routine functions and analysis (dependent upon experience) as required by the specific laboratory requirement in compliance with B. Braun and cGMP specifications. | 1/20/2023 |
| 5396 | Aesculap Irvine, CA QC Microbiology Associate II Bachelor's degree in a Science related field preferred. Exp: 01-02 years |
Performs routine functions and analysis (dependent upon experience) as required by the specific laboratory requirement in compliance with B. Braun and cGMP specifications. | 1/20/2023 |
| 5397 | Aesculap Irvine, CA Microbiologist (QC Micro Duplex) Bachelor's degree required. Exp: 0-02 years |
The individual will be part of microbiological method validations for the site. This individual will work specifically in Aseptic Fills and Isolators Independently execute existing lab equipment re-qualification and new equipment qualification for the Duplex Facility. Perform variety of routine and non routine tasks including non-conformance and OOS investigation for laboratory and manufacturing operations, writing investigation reports, protocols and updating procedures and other documents. Support other projects assigned as required by the department. | 1/20/2023 |
| 5398 | Aesculap Irvine, CA QC Chemistry Associate II (QC Chem Duplex) Bachelor's degree in a Science related field preferred. Exp: 01-02 years |
Perform routine laboratory analysis of In-Process, finished product, raw material, stability samples and environmental monitoring according to established specifications and procedures using wet chemistry techniques or various laboratory apparatus and instruments (e.g. HPLC, UV/Visible Spectrophotometer, FTIR, TOC, pH meter etc.) in compliance with B. Braun, cGMP, GLPs, SOPs, USP and FDA guidelines. | 1/20/2023 |
| 5399 | AGC Biologics Seattle, WA Process Technology Associate - Analytical Bachelor’s Degree or higher in engineering or other science-related field Exp: 0-3+years |
We have an exciting opportunity for a Process Technology Associate to join the Research and Development Center (RD Center) team at AGC Biologics. This is an opportunity to develop next-generation high-throughput analytical techniques through collaboration with the global AGC Biologics RD network. Additionally, this position is responsible for analyzing process samples for cell line development, upstream and downstream development groups within the RD Center. Support activities for the transfer of new technologies into current PD operations may be required. | 1/20/2023 |
| 5400 | Scanogen Baltimore, MD CHEMICAL AND BIOMOLECULAR ENGINEER Chemical Engineering degree Exp: 1+ years |
The main focus is to optimize and automate biomolecule detection assays. | 1/9/2023 |
| 5401 | ScienCell Research Laboratories Carlsbad, CA Associate Molecular Biologist Bachelor’s or Master’s degree in life science Exp: one-year |
Responsibilities include, but are not limited to, working on cell-derived DNA, RNA, and proteins purification, gene expression analysis, performing PCR/RT-PCT/qPCR, SDS PAGE and UV spectrum for quantitation. Candidates should be familiar with electrophoresis, spectrophotometer, centrifugation and other basic laboratory techniques. General lab logistical skills such as record keeping, ordering supplies and ensuring general laboratory safety and cleanliness are also required. | 1/9/2023 |
| 5402 | SeaGen Bothell, WA Manufacturing Support Associate I Bachelor’s degree preferably in Life Sciences or Engineering. Exp: 0-2 year |
The North Creek Manufacturing Facility at Seagen is seeking a Manufacturing Associate I to participate in cGMP activities in upstream production. The Associate will use their training and knowledge of biopharmaceutical manufacturing to execute operations in a cGMP facility. | 1/9/2023 |
| 5403 | Seran Bioscience Bend, OR Laboratory Technician I Bachelor’s degree or coursework in chemical engineering, chemistry, materials science, or related field preferred. Exp: 0-2 year |
Serán BioScience is looking for a laboratory technician to support and contribute to the development of custom formulations and process development for a variety of pharmaceutical clients. This role requires strong attention to detail and focus within a fast-paced work environment. Successful candidates will demonstrate strengths in teamwork, self-discipline, and proactive communication to ensure collective goals are achieved. Those with limited lab experience are still encouraged to apply. | 1/9/2023 |
| 5404 | Seran Bioscience Bend, OR Scientist/Engineer I, Formulation Sciences B.S. in Science or Engineering discipline. Exp: 0-3 years |
Serán is searching for an entry level scientist or engineer to join our Formulation Sciences team! With mentorship from senior team members, the formulation scientist will investigate the properties of novel pharmaceutical compounds, design formulation strategies to improve drug delivery, and characterize the performance of the enhanced formulations. The ideal candidate has strong communication and collaboration skills to excel in a fast-paced, interdisciplinary team environment. Experience with benchtop laboratory techniques is desired, but scientific curiosity and independent thinking are required for success. | 1/9/2023 |
| 5405 | Seran Bioscience Bend, OR Scientist/Engineer I B.S. or M.S. in Science or Engineering discipline. Exp: 0-3 years |
Serán seeks to hire an entry-level Scientist or Engineer to contribute to pharmaceutical R&D projects in the general area of drug delivery formulation and manufacturing processes. Candidates should possess a bachelor’s or master’s degree in chemistry, chemical engineering, biology, biological engineering, mechanical engineering, materials science and engineering, or physics. Demonstrated research experience is desirable. Candidates with additional relevant experience are also invited to apply. | 1/10/2023 |
| 5406 | Seres Therapeutics Cambridge, MA Research Associate / Senior Research Associate, Microbiology & Functional Screening (100% ON SITE) Bachelors or Masters in Microbiology, Immunology or related scientific field. Exp: BS: +1 year; MS: +0 year |
Seres Therapeutics is seeking experienced and highly-motivated Research Associate to join our Microbiology and Functional Screening team to develop and implement high throughput functional screens that advance the company’s Ecobiotic® therapeutics discovery programs in oncology, infectious and inflammatory diseases. As a member of the Microbiology and Functional Screening team, you will work intimately with research teams across the organization to translate critical insights in the field of the human microbiome into therapeutic leads. The successful candidate will be innovative, thrive in an intense and dynamic environment, and use his/her creative and imaginative problem solving skills to help bring new products to patients. | 1/10/2023 |
| 5407 | Smithers Wareham, MA Associate Chemist I - Environmental Fate and Metabolism B.S. degree in chemistry or related field Exp: 6 months |
Position is expected to perform a variety of routine tasks and often complex and difficult procedures independently and under supervision, in support of the conduct of normal laboratory operations. Individual is expected to detect and report problems in standardized procedures due to instrumental, sample, or test system failures. Performs a variety of routine, laboratory-based procedures. Responsible for understanding and routinely performing applicable Standard Operating Procedures, study specific protocol procedures and other laboratory assignments. This often includes recording instrument and apparatus readings on standard forms, preparation of test systems and recording and compiling laboratory data in real time in a complete and thorough manner for individual assignments. Responsible for maintaining cleanliness of the labs, storage and chamber areas as well as executing regular maintenance/calibration of equipment used on a regular basis. Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations as well as company policies. Duties are performed with minimal supervision. | 1/10/2023 |
| 5408 | Smithers Wareham, MA Associate Chemist I - Chemistry Bachelors or better in Chemistry or related field. Exp: 6 months |
Position is expected to perform varied and often complex and difficult procedures somewhat independently. Individual is expected to detect and report problems in standardized procedures due to instrumental, sample, or test system failures. Operates and may maintain, under supervision, test equipment and apparatus of moderate complexity. May provide information for initial data interpretation and test system conformance to expectations. Records, compiles and reduces laboratory data in real time in a complete and thorough manner for individual assignments. May produce reports. | 1/10/2023 |
| 5409 | Smithers Wareham, MA Assistant Biologist - Ecotoxicology Bachelors or better in Biology or related field. Exp: 6 months |
Often, duties include recording instrument and apparatus readings, making observations of various biological effects in exposures and compiling study data books. Incumbent will be introduced to mathematical and statistical procedures used to reduce and analyze study data. Responsible for maintaining cleanliness of the labs, storage and culture areas including maintenance and calibration of equipment used in any of these settings. May require routine involvement in seawater and/or sediment collection. Assignments are completed with minimal supervision. Assists with organization, direction and training of technicians. Assists in coordinating internal requirements for testing (i.e. chemistry support, Quality Assurance, reporting). Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations and company policies. | 1/10/2023 |
| 5410 | Smithers Wareham, MA Smithers Cannabis Testing Services Division, MA - Associate Chemist I BS. degree in chemistry or related field. Exp: 6 months |
Essential Functions: Cannabis sample processing of flower, concentrates, extracts, and infused products. Cannabis sample extraction & dilutions. Routine maintenance of laboratory equipment and instrument calibration. Wash glassware used by the laboratory. Accurate entry of sample data into LIMS. Production of laboratory reagents and stocks. | 1/10/2023 |
| 5411 | Smith and Nephew Fort Worth, TX QC Microbiologist 1 Bachelor of Science in Microbiology or related scientific discipline required Exp: 1 - 3 years |
This position will perform in a GMP environment following FDA and ICH guidelines. Duties include product release testing per USP Microbial Limits testing, product stability testing, environmental sampling of controlled ISO 5-8 classified areas and controlled unclassified areas, preparation of media and cultures, growth promotion, purified water sampling, preparation and sterilization of equipment. | 1/10/2023 |
| 5412 | Smith and Nephew Fort Worth, TX QC Microbiologist 1 Bachelor of Science in Microbiology or related scientific discipline required Exp: 1 - 3 years |
This position will perform in a GMP environment following FDA and ICH guidelines. Duties include product release testing per USP Microbial Limits testing, product stability testing, environmental sampling of controlled ISO 5-8 classified areas and controlled unclassified areas, preparation of media and cultures, growth promotion, purified water sampling, preparation and sterilization of equipment. | 1/10/2023 |
| 5413 | Smiths Medical Austin, TX Chemistry Analyst I - Nights - (22301793) Bachelor’s Degree is required: Chemistry, Chemical Engineering, or Chemical Science Exp: 0-2 year |
The Chemistry Analyst I will work under direct supervision or be partnered with an experienced analyst to perform wet chemistry analyses, preparation of reagents, standardization of solutions, and instrumentation testing and documentation in a cGMP environment. May be cross-trained to work in other laboratory areas as dictated by the needs of the department. | 1/10/2023 |
| 5414 | Sofregen Medical Framingham, MA Quality Engineer Bachelor’s degree in scientific discipline. Exp: 0-2 years |
Sofregen Medical is seeking a Quality Engineer to join our Manufacturing team and support the production of Sofregen’s commercial silk-based medical device platform. The Quality Engineer plays a vital role in the maintenance of the Quality Management System as well as the daily operation of the laboratory. Duties will include maintaining a system to track equipment calibration & maintenance, environmental monitoring, inventory management, receiving and incoming inspection, and authoring routine Quality Control documentation (e.g. deviations, standard operating procedures (SOPs), batch records, etc.). The Quality Engineer will further collaborate with Manufacturing members to provide general support to critical processes. | 1/10/2023 |
| 5415 | Sonosite Mesa, AZ PROCESS ENGINEER - CMP BS in Chemical Engineering Exp: Zero to two years |
The CMP Process Engineer provides engineering and technical support to the CMP Manufacturing team to assure that all products manufactured meet the quality and cost requirements of the CMP business, and the quality, volume, and availability requirements of our customers. The CMP Process Engineer also assures that all ongoing operations and any proposed expansion of operations fully meet the EH&S targets and objectives for the Mesa site. | 1/10/2023 |
| 5416 | Spotlight Therapeutics Hayward, CA Research Associate (RA) - Protein Engineering BS/MS in Biochemistry, Molecular Biology, Genetics, or related field Exp: 1-2 years |
Primary responsibilities will include several aspects of protein engineering, such as plasmid construct design, protein expression, and purification. In addition, biochemical assays would be carried out to assess purity, concentration, stability, integrity, and enzymatic activity of RNPs. This position requires a minimum of 1-2 years of laboratory experience, with demonstrated expertise in biochemistry and molecular biology. Ideally, the candidate will have experience with molecular cloning, the production of recombinant proteins, and the design and execution of biochemical assays. | 1/10/2023 |
| 5417 | Spotlight Therapeutics Hayward, CA Research Associate (RA) - Monogenic Diseases BS/MS in molecular biology, cellular biology, or related field Exp: 1-2 years |
We are looking for an enthusiastic research associate to join our biology team. This candidate will help develop various primary cell models, be responsible for testing engineered RNPs, and evaluate downstream editing. The candidate will also help in identifying disease targets and will screen guides for different disease indications. This individual will work across different teams to advance numerous projects. The candidate will have opportunities for professional growth and development in a fast-growing biotechnology start-up. | 1/10/2023 |
| 5418 | Stability Biologics San Antonio, TX QA Specialist - San Antonio, TX BS degree in a scientific discipline (Chemistry, Biology, Physics, Bio-Medical Engineering/Chemical Engineering, etc.) Exp: 1 year |
The Quality Assurance Specialist (QAS) will be a member of the Stability Biologics Quality Dept. to perform quality record reviews, batch release, record retention, data entry, auditing, investigations and document control activities. The QAS will be responsible for quality assurance metrics, CAPA/NCMR and maintaining all quality records/batch records in a secure and controlled manner. The QA Specialist will also be responsible for ensuring all policies and procedures are in compliance with appropriate FDA, AATB, states, and Stability Biologics standard operating procedure. | 1/10/2023 |
| 5419 | Stellartech Research Milpitas, CA Quality Engineer II BS degree or equivalent. Exp: 1-3 years |
Stellartech is looking for a Quality Engineer to join our Team. | 1/11/2023 |
| 5420 | Strand Therapeutics Boston, MA Associate Scientist, LNP Discovery B.S. or M.S. in Pharmaceutical Sciences, Biomedical Engineering, Chemical Engineering or other relevant scientific disciple. Exp: 1-3+ years |
We are looking for a highly motivated and innovative candidate for the role of Associate Scientist, LNP Discovery. The expectation is that the candidate will have experience in the formulation and characterization of LNPs. The candidate will be expected to work in an innovative, fast-paced, cross-collaborative biotech environment and contribute in multi-disciplinary team activities to advance our platform. This role will have the opportunity to collaborate with functions outside of LNP Discovery such as Translational biology, LNP Process Development, and Analytical Development. | 1/11/2023 |
| 5421 | Strand Therapeutics Boston, MA Associate Scientist/Sr Associate Scientist, RNA Discovery Biology M.S. Exp: 1 year |
We are looking for an Associate Scientist/Sr Associate Scientist to support our molecular and cell biology needs to enable the drug discovery efforts within the RNA Discovery Biology team at Strand Therapeutics. The ideal candidate will have experience in mammalian cell culture including primary cell isolation and handling. The candidate will be expected to work in an innovative, fast-paced, cross-collaborative biotech environment and contribute in multi-disciplinary team activities to advance our platform. | 1/11/2023 |
| 5422 | Strand Therapeutics Boston, MA Associate Scientist, In Vivo Pharmacology B.S. or M.S. in Biological Sciences, Bioengineering or related discipline. Exp: 1-3+ years |
We are looking for an Associate Scientist to join the In Vivo Pharmacology group to conduct proof-of-concept, validation, and pharmacology studies to support multiple pre-clinical programs. You will be passionate about scientific discovery, undeterred by bold challenges, and enjoy working as a team to develop the next generation of mRNA medicines. You should be highly organized, a critical thinker, adaptable to changing priorities, and possess a strong ability to collaborate effectively with teams of diverse backgrounds. | 1/11/2023 |
| 5423 | Surgalign San Diego, CA Quality Engineer Bachelor’s Degree in Engineering, or related field required Exp: 1-3 years |
The Quality Engineer works on a cross-functional team including Research & Development, Marketing, Regulatory, Supply Chain, and others to support new product development, specifically with review of design control documentation such as design and development plans, inputs, outputs, and verification and validation activities. Additional activities include drafting project quality plans, standard operating procedures, risk management, and test protocols/reports. | 1/11/2023 |
| 5424 | Taconic Biosciences Rensselaer, NY Senior Laboratory Specialist Molecular Analysis Bachelor’s Degree from a four-year college or university. Exp: 1 year |
The Senior Laboratory Specialist performs a variety of molecular assays on animal samples and must be able to generate high-quality results in a timely manner. This individual should be comfortable working in a high-throughput environment and be able to use proper judgement to make technical decisions on assay performance issues. | 1/11/2023 |
| 5425 | Tessera Therapeutics Somerville, MA Research Associate/Senior Research Associate, Cell Therapy Discovery BS/MS degree in biological sciences Exp: 1+ years |
We are looking for a Research Associate to join the Cell Therapy Discovery team to advance early-stage cell-based research with Tessera’s novel Gene Writing and Gene Rewriting technology for ex vivo and in vivo cell therapy applications. The Senior Research Associate will work closely with scientists in the Cell Therapy team to translate novel gene writing technologies to develop innovative therapeutics for Oncology disorders. We are searching for a driven, enthusiastic and self-motivated individual who is comfortable multitasking and working independently on various aspects of the platform. This individual will join a dynamic, rapidly growing, and highly collaborative team. | 1/11/2023 |
| 5426 | Tessera Therapeutics Somerville, MA Research Associate I/II, High Throughput Synthesis BS/MS degree. Exp: 0-3+ years |
The Research Associate I/II will be responsible in designing, synthesizing and purifying oligonucleotides for research studies and high throughput format. We are searching for a driven, enthusiastic, and self-motivated individual who is comfortable multitasking and working independently on various aspects of the platform. This individual will join a dynamic, rapidly growing, and highly collaborative team. | 1/11/2023 |
| 5427 | Tessera Therapeutics Somerville, MA Research Associate/Senior Research Associate, Stem Cell Biology BS/MS degree in biological sciences Exp: 1+ years |
We are looking for a Research Associate to join the In Vivo Rewriting Candidate Development team to advance translational research with Tessera’s novel Gene Writing and Gene Rewriting technology for in vivo gene therapy applications. The Research Associate will work closely with scientists to translate novel gene writing technologies to develop innovative therapeutics. We are searching for a driven, enthusiastic, and self-motivated individual who is comfortable multi-tasking and working independently on various aspects of the platform. This individual will join a dynamic, rapidly growing, and highly collaborative team. | 1/11/2023 |
| 5428 | Tri-Pac South Bend, IN Associate Engineer Bachelor’s degree in Engineering or equivalent. Exp: 0-2 years |
The Associate Engineer is a team player who can work independently or in a team setting with minimal supervision. He/she must possess good communication skills which will be used to contribute to ongoing initiatives, is detail oriented and task driven towards learning various systems and device functions. The Associate Engineer is actively involved with validation and quality activities required to support the Production Department. | 1/11/2023 |
| 5429 | Tris Pharma Monmouth Junction, NJ Associate QC Analytical Chemist Bachelors in Chemistry or related scientific field. Exp: 0-3 years |
We have an immediate opening in our Monmouth Junction, NJ QC Lab for an (Associate) QC Analytical Chemist. This is an entry level scientific position and we will train qualified candidates who meet listed requirements. Recent college graduates are welcome to apply. The (Associate) Quality Control (QC) Analytical Chemist performs analytical testing of raw materials, packaging components, in-process (IP), finished product (FP), and/or stability samples (ST). She/he is also responsible for following Analytical Methods, current Good Manufacturing Practices (cGMPs), Protocols, Standard Operating Procedures (SOPs) and company policies. | 1/11/2023 |
| 5430 | TScan Therapeutics Waltham, MA Research Associate/Senior Research Associate, In Vivo Pharmacology (RA07-7) For RA level: BS; For Sr. RA level:MS Exp: RA: 0-3+ years ; Sr. RA: 0-2+ years |
TScan Therapeutics is a startup biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for a motivated researcher to join our In Vivo Pharmacology team as a Research Associate/Senior Research Associate, supporting the preclinical development of our lead therapeutic TCRs. The ideal candidate should have relevant experience in in vivo pharmacology, mechanism of action and anti-tumor efficacy studies, and enjoy fast-paced, collaborative, and vibrant startup culture. A team player with a sense of urgency will thrive in this role. | 1/12/2023 |
| 5431 | TScan Therapeutics Waltham, MA Research Associate/Senior Research Associate, TCR Discovery (RA05-9) B.S. or M.S. Exp: B.S: 0-5 years; MS: 0-2 years |
TScan Therapeutics is a startup biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for an experienced researcher to join our team as Research Associate or Senior Research Associate, supporting our novel TCR discovery workflow in house. The ideal candidate should have relevant experience in T cell immunology, cancer cell culture and flow cytometry, and enjoy fast-paced, collaborative, and vibrant startup culture. A team player with a willingness to learn will thrive in this role. | 1/12/2023 |
| 5432 | Turn Biotechnologies Mountain View, CA Research Associate / Sr. Research Associate - Biology BS/MS in biology, biochemistry, molecular biology, or related discipline. Exp: one year |
Turn Biotechnologies is currently seeking a qualified, highly motivated individual for the position of Sr. Research Associate – Biology. This person will be a highly motivated and responsible individual whose primary purpose is to perform and assist with experiments, analyze data, maintain records, manage projects, maintain lab operations, and other duties as required to meet company goals. | 1/12/2023 |
| 5433 | Twist Bioscience South San Francisco, CA Research Associate B.S. or M.S. in Molecular Biology, Biochemistry, Chemistry or a closely-related field Exp: 0-2 years |
In this position, you will have the opportunity to work on leading-edge products for genomics, diagnostics, and personalized medicine. First and foremost, we are looking for someone with a scientist’s mindset. Creativity, critical thinking, careful experimental execution, and a desire to learn deep technical details are a must. This position is geared towards working with the DNA and RNA product lines. The candidate must be capable of maintaining current products, troubleshooting control fragment assembly issues, and analyzing data related to current and future controls. Up-and-coming scientists that demonstrate self-motivation and enthusiasm for scientific bench work are strongly encouraged. Your work will be mainly at the bench; however, you will have the opportunity to use high-throughput robotic instruments as well as coding and bioinformatics tools to expand your expertise. You will work alongside and learn from some of the best scientists and bioinformaticians in the business. | 1/12/2023 |
| 5434 | Twist Bioscience South San Francisco, CA Research Associate, Antibody Engineering BS Exp: 1-year |
We are seeking an outstanding, innovative, and creative Research associate to join our antibody discovery effort. This research associate will play multiple roles within the Biopharma group and will work within a team responsible for antibody discovery utilizing a number of in vitro display technologies, e.g. phage display, ribosome display, and yeast display. | 1/12/2023 |
| 5435 | Twist Bioscience South San Francisco, CA Research Associate, Flow Cytometry Bachelor’s degree in Biology, Biotechnology, or a related scientific discipline Exp: 0-3 years |
We are seeking a motivated individual to join our expanding flow cytometry team. Using state-of-the-art technology, the candidate would help accelerate our antibody discovery process through careful cell culture maintenance and flow cytometry screening. Highly qualified candidates will have experience with a variety of mammalian-based cell culture methods and techniques. Prior flow cytometry experience is desired. | 1/12/2023 |
| 5436 | Twist Bioscience South San Francisco, CA Research Associate, NGS Bachelors/ Associates degree in biology, chemistry, biochemistry Exp: 1-3 years |
Twist is seeking a highly motivated individual to help support customers and their Next Generation Sequencing needs. This individual will work closely with R&D and Customer Support teams to help develop custom solutions for various sequencing applications. The candidate will be detail oriented who is compatible with fast paced environments. | 1/12/2023 |
| 5437 | Twist Bioscience South San Francisco, CA Research Associate, NGS Viral Controls B.S. or M.S. in Molecular Biology, Biochemistry, Chemistry or a closely-related field. Exp: 0-2 years |
This position is geared towards working with the DNA and RNA controls product lines. The candidate must be capable of maintaining current products, troubleshooting control fragment assembly issues, and analyzing data related to current and future controls. Up-and-coming scientists that demonstrate self-motivation and enthusiasm for scientific bench work are strongly encouraged. Your work will be mainly at the bench; however, you will have the opportunity to use high-throughput robotic instruments as well as coding and bioinformatics tools to expand your expertise. You will work alongside and learn from some of the best scientists and bioinformaticians in the business. | 1/12/2023 |
| 5438 | Twist Bioscience South San Francisco, CA Research Associate, Process Development B.S. Molecular Biology, Biochemistry, Chemistry, or a closely-related field. Exp: 1-4 years |
We are looking for an outstanding Research Associate to join our Specialty Production Team in South San Francisco. The Research Associate will support the production team’s custom DNA-based applications and assays for synthetic biology including high-throughput gene synthesis, high-throughput cloning processes, and NGS-based QC. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast-paced startup environment. The ideal candidate will work independently, be very organized, have excellent molecular biology knowledge and skills, and communicate effectively with peers/management. The Candidate must be comfortable working in a LEAN manufacturing/ controlled laboratory environment. | 1/12/2023 |
| 5439 | Ultragenyx Pharmaceutical Cambridge, MA Senior Research Associate, Vector Core - Gene Therapy MSc in Biology, Molecular Biology, Biochemistry, Virology or cognate discipline. Exp: 1-3 years |
Reporting to the Senior Director of Vector Platform Research, the Senior Research Associate will support and execute the production and purification of rAAV from HEK and HeLa Producer Cell Line systems, as well as iterative improvement of these processes by performing hypothesis-driven research. This role will place specific emphasis on the downstream purification of rAAV including chromatography (primarily with AKTA FPLC systems), filtration processes, and final formulation of research grade material. | 1/12/2023 |
| 5440 | Proteintech Rosemont, IL Scientist I, Bioconjugation Bachelor’s degree in an appropriate area of specialization (Molecular Biology, Cell Biology, Biochemistry, or related life sciences). Exp: New grads |
New grads with lab experience are encouraged to apply. The successful candidate will support the development and optimization of processes in bioconjugation of antibodies for use in various applications like Flow Cytometry and IHC. | 1/2/2023 |
| 5441 | Pyxant Labs Salt Lake City, UT QC Reviewer II Bachelor of Science/Arts (BS/BA) degree. Exp: One year |
Reviews data for accuracy and compliance to applicable Standard Operating Procedures (SOPs) and regulations. Maintains and expands knowledge of regulatory requirements, SOP requirements, and client requirements. Performs follow up actions to reduce departmental citations from QA as needed. Maintains error tracking data in support of departmental improvement efforts. | 1/2/2023 |
| 5442 | Quanterix Billerica, MA Manufacturing Associate I, Downstream BS in Chemistry, Biology or related Life Sciences Exp: 0+ years |
We are looking for an experienced and motivated candidate to join our Manufacturing team. This individual will work with a team of individuals to prepare solutions, conjugate beads, reconstitute antigens and perform filling activities to support a diverse assay menu. | 1/2/2023 |
| 5443 | Quanterix Billerica, MA Manufacturing Associate I Upstream BS in Chemistry, Biology or related Life Sciences required. Exp: 1+ years |
We are looking for an experienced and motivated candidate to join our Manufacturing team. This individual will work with a team of individuals to prepare solutions, conjugate beads, reconstitute antigens and perform filling activities to support a diverse assay menu. | 1/2/2023 |
| 5444 | Quidel San Diego, CA Bioengineer Master’s degree in biochemistry, chemistry, physics, bioengineering, related field, or equivalent. Exp: 1 year |
Quidel is looking for a Bioengineer to join our team in the Mira Mesa area of San Diego. The Bioengineer provides technical expertise to the design and development of new and novel medical device product(s). Designs and implements new methodologies, materials, machines, processes, or products. Develops new concepts from initial design to market release. Conducts feasibility, development, verification and validation studies of the design to determine the product’s ability to function as intended. Maintains detailed documentation throughout all phases of research and development. Coordinates activities with outside suppliers and consultants to ensure the delivery of supplies or services needed to meet scheduled timelines. | 1/2/2023 |
| 5445 | Quidel San Diego, CA Development Associate II (Assay Development) MA/MS in life sciences. Exp: 0-2 years’ |
Responsibilities include activities to support research and new product development. Perform self-directed experiments or as directed by Scientist or Manager. | 1/3/2023 |
| 5446 | Quotient Sciences Garnet Valley, PA Associate Formulator B.S. Degree in Chemical Engineering, Pharmacy/Pharmaceutical Sciences or other related field. Exp: 0-2 years’ |
To conduct formulation development and manufacturing related activities. To comply & adhere to Good Manufacturing Practice (GMP) standards. | 1/3/2023 |
| 5447 | QuVA Pharma Bloomsbury, NJ Sterility Assurance Specialist 2nd shift Bachelors or better in Microbiology or related field. Exp: 1-2 years |
Schedule & Proctor Media Fills Performs reading of media aseptic process simulations and Environmental/Personnel Monitoring (EM/PM) plates and accounting of all units Performs EM/PM sampling Maintains EM/PM records Periodically reviews Environmental/Personnel monitoring data to identify any potential trends Providing training support for personnel on appropriate aseptic techniques and gowning techniques including execution of Compounder Competency Assessments | 1/3/2023 |
| 5448 | QuVA Pharma Bloomsbury, NJ Sterility Assurance Specialist 1st shift Bachelors or better in Microbiology or related field. Exp: 1-2 years |
Schedule & Proctor Media Fills Performs reading of media aseptic process simulations and Environmental/Personnel Monitoring (EM/PM) plates and accounting of all units Performs EM/PM sampling Maintains EM/PM records Periodically reviews Environmental/Personnel monitoring data to identify any potential trends Providing training support for personnel on appropriate aseptic techniques and gowning techniques including execution of Compounder Competency Assessments | 1/3/2023 |
| 5449 | QuVA Pharma Bloomsbury, NJ Chemist 1st shift B.S. or M.S. degree in chemistry, biology or related field. Exp: 0- 2 years |
Reads and understands SOPs and follow policy, procedure and applicable government regulations, such as current Good Manufacturing Practices (cGMP), DEA compliance, quality standards and safety requirements Provide analytical data in a timely manner. This includes understanding of Supervisor or Manager’s expectations Provide input to R&D SOPs to enhance the efficiency of the laboratory Keep accurate notebook records in accordance with SOPs, cGMP and current Good Documentation Practices (cGDP) requirements Communicate as needed any testing issues to either a Supervisor or Manager or to a cross-functional group such as Metrology | 1/3/2023 |
| 5450 | QuVA Pharma Bloomsbury, NJ Chemist 2nd shift B.S. or M.S. degree in chemistry, biology or related field. Exp: 0- 2 years |
Reads and understands SOPs and follow policy, procedure and applicable government regulations, such as current Good Manufacturing Practices (cGMP), DEA compliance, quality standards and safety requirements Provide analytical data in a timely manner. This includes understanding of Supervisor or Manager’s expectations Provide input to R&D SOPs to enhance the efficiency of the laboratory Keep accurate notebook records in accordance with SOPs, cGMP and current Good Documentation Practices (cGDP) requirements Communicate as needed any testing issues to either a Supervisor or Manager or to a cross-functional group such as Metrology | 1/3/2023 |
| 5451 | Rani Therapeutics San Jose, CA MECHANICAL ENGINEER Bachelor’s Degree in Mechanical Engineering Exp: 1-3 years |
We are seeking an exceptional Mechanical Engineer to design and develop semi or fully automated equipment that are used for high volume, disposable devices. Your role is to find creative and sound engineering solutions to challenging problems with strong focus on quality, reliability and execution. This is a hands-on position that requires interaction and collaboration with a cross-functional team including Engineering, Manufacturing, Biology, Quality, Facilities and Sustaining. | 1/3/2023 |
| 5452 | Rapid Micro Biosystems Lowell, MA Research Associate I Bachelor’s degree in Microbiology, or Biological sciences. Exp: 0-2 years’ |
We are seeking Research Associate I for the R&D Microbiology group based in Lowell, MA emphasizing teamwork, creativity, and intellectual achievement. The candidate will have the opportunity to work closely with our highly skilled scientists and engineers on a variety of cross-functional projects in developing new applications, technologies, and products for rapid microbial enumeration assays. You should be an energetic self-starter with documented productivity and integrity; strong organizational, interpersonal, and communication skills required. | 1/3/2023 |
| 5453 | Reaction Biology Malvern, PA Research Associate I – Biochemical Assays Bachelor’s Degree or equivalent in biochemistry or related discipline Exp: 0-3 years |
Reaction Biology (RB) is a private pharmaceutical research company. We provide contract research services to over 1500 clients worldwide through our labs in Malvern, PA and Freiburg, Germany. We are currently seeking a Research Associate I for our Malvern, PA facility. We are looking for a reliable and motivated individual with a strong science background to work in our lab. The position is a bench position with the primary duty of executing a variety of enzymatic assays. | 1/4/2023 |
| 5454 | Reata Pharmaceuticals Irving, TX Research Associate, Molecular and Cell Biology BSc in biological sciences Exp: 1 - 3 years |
We are looking for a Research Associate with basic knowledge of cell biology and biochemistry to join our dynamic team of researchers. With guidance, the successful candidate will be expected to execute routine experiments in support of our drug discovery and development programs. Demonstrated technical proficiency and capacity for problem-solving are a plus. Ability to work in a fast-paced environment with rapidly changing priorities is desired. | 1/4/2023 |
| 5455 | Replimmune Framingham, MA Validation Associate Bachelor’s degree in science, Technology, Engineering, and/or Math (STEM) field is preferred. Exp: one-year |
The Validation Associate is responsible for the maintenance and execution of validation protocols for qualification and requalification of equipment at the Framingham, MA, manufacturing facility in accordance with appropriate regulatory guidance. The individual will work with equipment vendors and external contractors to coordinate scheduling, execution and review of qualification protocols / reports. The Validation Associate’s primary responsibility is to perform field executions for various protocols necessary for GMP equipment and systems. The individual will contribute to maintaining the validated status of the facility and equipment through calibration, performance monitoring, data integrity assessments, and requalification activities. | 1/4/2023 |
| 5456 | R & D Systems Austin, TX Research Associate Bachelor’s degree in biology, chemistry, biomedical engineering, or related field is required. Exp: 1-3 years |
Asuragen is seeking an outstanding BSc-level scientist to join our Research group. This is a full time position focused on developing innovative nucleic acid or protein-based technologies. This role will support new product initiatives to enable novel, multiplexed-PCR technologies that can resolve multiple classes of DNA/RNA markers or proteomics through integration of reagents, instrumentation, analysis algorithms and software. Platforms used in our laboratory include quantitative real-time PCR, digital PCR, capillary electrophoresis, next-generation and long-range sequencing. | 1/5/2023 |
| 5457 | R & D Systems Minneapolis, MN Research Associate, Mammalian Cell Culture Bachelor’s degree in a biological science. Exp: 0 to 2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for recombinant protein production, media and supplement preparation, and additional duties as assigned. This position requires a Tuesday through Saturday workweek. | 1/5/2023 |
| 5458 | R & D Systems Minneapolis, MN Quality Technician MLT/MLS degree, Bachelor’s degree in Biology, or related field of study. Exp: 0-1 year |
This position will require setup, maintenance, troubleshooting, and operation of QC hematology analyzers. This position will require monitoring instrument performance throughout the QC process and troubleshooting the instrument when necessary. This position will test hematology products for homogeneity during the bottling process by following established methods. The expectation for this position is to setup and QC product on 50% of the laboratory instruments and troubleshoot as necessary. You will assist the QC Laboratory Manager/Supervisor with releasing products to bottle and ship, proofing labels and assay sheets. You will serve as a member of the Technical Service team by rotating through our Technical Service Department and responding to customer inquiries and complaints with the assistance of senior members of the department. This position will adhere to safety regulations. Perform additional duties as assigned. | 1/5/2023 |
| 5459 | R & D Systems San Marcos, CA Research Associate - Advanced Bachelor’s degree in Chemistry, Biochemistry, Biological Science, or related field preferred. Exp: 1-5 years |
Responsible for developing controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for developing quality products on schedule. General knowledge and basic application of concepts, theories, terminology and practices that apply to research in a laboratory environment. | 1/5/2023 |
| 5460 | Roche Carlsbad, CA Research Associate II Assay Development M.S. in Bioengineering, Biochemistry, Molecular Biology, Analytical Chemistry or a related field. Exp: 0+ years |
The Research Associate II will execute a range of molecular biology and bioanalytical procedures, reagent preparation, and laboratory duties under supervision. You will investigate, adapt or modify experimental methods and technologies for project advancement. This is a unique opportunity to leverage your background and skills in molecular diagnostics to enhance and build your career by working cross-functionally. An exciting career opportunity where your contributions will impact business opportunities through successful completion of projects. | 1/5/2023 |
| 5461 | Roivant Sciences Boston, MA Research Associate, Automation and Assay Operations (Covant Therapeutics) Sc. or M.Sc. degree in biology, biochemistry, organic, analytical chemistry or related discipline. Exp: 1+ years |
The successful candidate will have a background in laboratory automation techniques and ideally have a track record of accomplishments in academia or in the life sciences/pharmaceutical/biotechnology industry. Our group is committed to the professional and scientific growth of our team members. As a result, s/he must have a strong desire to learn. The successful candidate will have the opportunity to acquire novel analytical and scientific skills and will be exposed to cross-functional and collaborative drug discovery in a biotechnology environment. | 1/5/2023 |
| 5462 | SAMDI Tech Chicago, IL Research Assistant B.S. in biology, biochemistry, chemistry, or related field. Exp: 0-3 years |
The Research Assistant will be an active member of our dynamic Research Team. The Research Team leads target/enzyme-based projects for biotech and pharma clients to develop biochemical assays for high-throughput screening and characterization of drug candidates and reaction mechanisms. | 1/5/2023 |
| 5463 | Sanofi Pasteur Waltham, MA BioProcess Analytics Research Associate BS in biological sciences or related field. Exp: 0 – 2 years |
The BioProcess Analytics support group located in Waltham, MA is responsible for execution of analytical methods to support manufacturing and development activities, building process understanding, and supporting life cycle management from early to late stage clinical entry. The Research Associate (Analytical Technician) is responsible for executing test methods under control of established procedures. We are looking for a candidate that has experience in an analytical setting that can independently manage and execute their testing schedule supportive of genomic medicines process development. In addition, they should possess the skills to interpret and communicate their data with the appropriate development teams. | 1/5/2023 |
| 5464 | Sanofi Pasteur Waltham, MA mRNA, Research Associate, Gene Synthesis - Vaccine M.S. in a related field (e.g., Chemical Engineering, Biochemical Engineering, Biochemistry, Biotechnology). Exp: 1-3 years |
As an experienced Plasmid DNA Research Associate, you will be responsible for supporting the efforts to establish a high throughput gene synthesis workflow initiating with design and ending in analytical methodologies. | 1/5/2023 |
| 5465 | Sanofi Pasteur Framingham, MA Senior Research Associate Master's degree in Biochemistry, Pharmaceutical Sciences, Chemical Engineering, Biological Engineering. Exp: 0+ years |
We are seeking a highly motivated and talented Senior Research Associate (SRA) to join our Formulation and Process Development (FPD) group. FPD is part of the global Biologics Drug Product Development & Manufacturing group, a critical R&D function enabling the manufacturing of stable and deliverable dosage forms along the complete development timeline from molecule selection to commercial tech transfer. The selected candidate will be responsible primarily for formulation and process development for protein and monoclonal antibody therapeutics for liquid and lyophilized dosages. Key expectations and training will include solid understanding in protein structure, chemistry, and characterizations. You will be part of a team with global responsibility for formulation and process development for Protein therapeutics and Gene Therapy. The candidate will have the opportunity to work on different facets of drug product formulation and process development for different modalities such as monoclonal antibodies (mAb), multi-specific antibodies, therapeutic enzymes, fusion proteins, viral capsids (recombinant AAV and Lentiviral vectors), Lipid Nanoparticles and Cell Therapies | 1/5/2023 |
| 5466 | Sanofi Pasteur Framingham, MA Research Associate Cell Culture Development Bachelor's degree in Chemical Engineering, Biochemical Engineering, Biochemistry or related discipline. Exp: 0+ years |
We are looking for candidates for a position at the level of Research Engineer. This individual will join a dynamic and motivated team to develop cell culture processes in support of early and late stage drug development programs, as well as tech transfer of the developed process into the clinical manufacturing team or Industrial Affairs organization. She/he will evaluate new technologies and develop platform technologies suitable for incorporation into our upstream process. He/she will ensure that the highest standards of safety and environmental compliance are maintained in the workplace and operate under the regulatory requirements for biologics product development and manufacturing. | 1/5/2023 |
| 5467 | Sanofi Pasteur Cambridge, MA Research Associate - Biomarkers and Clinical Bioanalyses Bachelor’s degree or Master’s degree in the field of immunology, biochemistry, biology, or other life-science field. Exp: BS: 1-3 years’; MS: 0-2 years |
We are seeking a Research Associate to join the Bioanalysis group within Biomarkers & Clinical Bioanalysis (BCB), a global department within the Translational Medicine and Early Development unit of Sanofi. This position will work in a team setting to develop and validate assays, as well as support sample analysis in a regulated environment. The primary laboratory responsibilities of this position require the candidate to be on-site 5 days a week. | 1/5/2023 |
| 5468 | Sanofi Pasteur Framingham, MA Senior Research Associate Purification Process Development Master's degree in Chemical Engineering, Biochemical Engineering, biochemistry or related discipline. Exp: 0+ years |
We are looking for candidates for the position of Senior Research Associate. This individual will join a dynamic and motivated team to develop downstream purification processes in support of early and late-stage drug development programs. In addition, the Senior Research Associate will support the tech transfer of the developed process into the clinical manufacturing team or Industrial Affairs organization, while ensuring the highest standards of safety, environmental, and regulatory compliance are maintained in the workplace. | 1/5/2023 |
| 5469 | Sanofi Genzyme Waltham, MA Senior Research Associate Drug Product Master’s degree in biochemistry, pharmaceutical science, chemical engineering, or a related discipline. Exp: 0+ years |
The Senior Research Associate will be a part of the Global Drug Product Development & Manufacturing group. The candidate will primarily support Biopharmaceutical Drug Product development projects for Gene Therapy (in support of the Genomic Medicine Unit) and Protein therapeutic programs. The candidate will have the opportunity to work on different facets of drug product development for different modalities such as Lipid Nanoparticles, gene therapy capsids (recombinant AAV capsids), Cell Therapy and Protein/Enzyme therapeutics | 1/5/2023 |
| 5470 | Sanofi Genzyme Swiftwater, PA Senior Production Technician - Vaccines Bachelors Exp: 1 + years |
This role is for a non-exempt employee working in the Filling Department. Their Bi-weekly pay is based on previous experience and education time. | 1/5/2023 |
| 5471 | Sanofi Genzyme Swiftwater, PA Fill LL-2 - Vaccines Associate or Bachelors' degree in Life Sciences or other relevant fields of study. Exp: no experience |
The production technician is the “heartbeat” of the vaccine manufacturing and is primarily responsible for the high quality and efficient production of our vaccines in accordance with current good manufacturing practices (cGMP) for all relevant regulatory agencies (e.g., FDA). | 1/5/2023 |
| 5472 | Sanofi Genzyme Waltham, MA mRNA, Research Associate, Gene Synthesis - Vaccine M.S. in a related field (e.g., Chemical Engineering, Biochemical Engineering, Biochemistry, Biotechnology). Exp: 1-3 years |
As an experienced Plasmid DNA Research Associate, you will be responsible for supporting the efforts to establish a high throughput gene synthesis workflow initiating with design and ending in analytical methodologies. | 1/5/2023 |
| 5473 | Sanofi Genzyme Waltham, MA mRNA - Senior Research Associate, Plasmid Production M.S. in a related field (e.g., Chemical Engineering, Biochemical Engineering, Biochemistry, Biotechnology). Exp: 1-3 years |
As an experienced molecular biologist, you will be supporting thedesign, development and implementation of a robust plasmid growth, extraction, and purification process for preclinical supercoiled and linearized plasmid production. | 1/5/2023 |
| 5474 | Sanofi Genzyme Waltham, MA Senior Research Associate Purification Process Development Master’s degree in chemical or biochemical engineering or related disciplines. Exp: 0+ years |
We are looking for a candidate with experience in AAV purification development, scale-up, and pilot manufacturing, and technology transfer. | 1/5/2023 |
| 5475 | Sarepta Therapeutics Durham, NC Contract Research Associate I B.S. degree in Molecular Biology, Biochemistry, Immunology, Cell Biology, Bioengineering, or related field. Exp: 1 year |
The Research Associate I provides laboratory support, performs experiments, and collects data on in vitro, ex vivo, and/or in vivo studies to investigate the effects of CRISPR-based gene editing on gene and protein expression, tissue pathology, and disease phenotype in animal models of neuromuscular and/or neurodegenerative disorders. This role provides laboratory support of day-to-day GCLP analyses and develops cutting-edge CRISPR-based technology platforms for research and therapeutic applications. | 1/5/2023 |
| 5476 | Sarepta Therapeutics Andover, MA QC Associate I BS in Chemistry or related science field. Exp: 0-2 years’ |
This individual will support quality control activities conducted both internally and at the Contract Test Laboratories (CTLs). The individual will be responsible for reviewing release and stability data, writing technical reports, supporting analytical method validation and qualification activities conducted at the CTLs. This individual will assist in transferring assays to and from domestic and overseas vendors and monitoring, compiling and reviewing data. The individual will also assist in managing quality events, data trending, review of quality documents originated at the testing laboratories as well as internally at Sarepta. All aspects of this position would involve working in a GMP compliant manner. | 1/5/2023 |
| 5477 | Sarepta Therapeutics Andover, MA Contract Laboratory Operations Assistant B.S degree in Biology, Chemistry, or related field. Exp: 2 years |
The Research Operations team at Sarepta Therapeutics is seeking a motivated laboratory operations associate to assist with routine laboratory operations and help implement compliance in a clinical laboratory setting. This includes day-to-day laboratory operations, sample and equipment management, and implementing new processes within the lab for laboratory compliance. | 1/5/2023 |
| 5478 | Sarepta Therapeutics Durham, NC Contract Research Associate I B.S. degree in Molecular Biology, Biochemistry, Immunology, Cell Biology, Bioengineering, or related field. Exp: 1 year |
The Research Associate I provides laboratory support, performs experiments, and collects data on in vitro, ex vivo, and/or in vivo studies to investigate the effects of CRISPR-based gene editing on gene and protein expression, tissue pathology, and disease phenotype in animal models of neuromuscular and/or neurodegenerative disorders. This role provides laboratory support of day-to-day GCLP analyses and develops cutting-edge CRISPR-based technology platforms for research and therapeutic applications. | 1/5/2023 |
| 5479 | Sarepta Therapeutics Andover, MA Contract Lab Operations Assistant Associate or B.S degree in Biology, Chemistry, or related field. Exp: 1 year |
This individual will support laboratory operations at Sarepta Andover, MA site. This individual will support the day-to-day laboratory operations including but not limited to reagent ordering, receiving and inventory, and sample and equipment management. All aspects of this position involve working in a GMP-compliant manner. | 1/5/2023 |
| 5480 | Olaris Therapeutics Framingham, MA RESEARCH ASSOCIATE B.S. or MS Degree in Biology, Biochemistry, Chemistry, or related field Exp: 1 - 3+ years |
The successful candidate will be responsible for a broad range of activities including metabolite extraction from patient biofluids, NMR and MS sample preparation and analysis, sample organization and handling. You will be responsible for maintaining a proper lab notebook. You will be expected to maintain a clean lab space and follow all safety guidelines. This position includes the opportunity to learn advanced NMR and MS techniques. | 12/26/2022 |
| 5481 | Ology Bioservices East Norriton, PA Research Associate I, Cell Therapy Process Development Bachelor’s or Master’s degree in immunology, cell biology, bioengineering or a related field. Exp: 0 - 2 years |
Resilience is seeking a talented Research Associate I to expand our cell therapy process development team. With the guidance of process development senior staff, this researcher will develop and optimize manufacturing processes for gene-modified cell products to advance Resilience’s biomanufacturing platforms and the clinical programs of Resilience’s partners. | 12/26/2022 |
| 5482 | Ology Bioservices East Norriton, PA Bioprocess Technician I Associates/Bachelor’s (science preferred) degree. Exp: 0-2 years |
The Technician I, Cell Therapy Manufacturing position is responsible for the hands-on clinical manufacturing of cell therapy product according to current Good Manufacturing Practices (cGMPs) and procedures. The position will work directly with a team of manufacturing technicians, specialists and scientists in Cell Therapy Manufacturing and Process Development and report to the Bioprocess and Cell Therapy Supervisor. | 12/26/2022 |
| 5483 | Ology Bioservices East Norriton, PA Bioprocess Technician II Associates/Bachelor’s (science preferred) degree. Exp: 1-3 years |
The Technician II, Cell Therapy Manufacturing position is responsible for the hands-on clinical manufacturing of cell therapy product according to current Good Manufacturing Practices (cGMPs) and procedures. The position will work directly with a team of manufacturing technicians, specialists and scientists in Cell Therapy Manufacturing and Process Development and report to the Bioprocess and Cell Therapy Supervisor. | 12/26/2022 |
| 5484 | Omniome Menlo Park, CA Quality Control Research Associate Bachelor’s degree in Biological/Life Sciences, Chemistry, Biochemistry, or related field. Exp: 1+ years |
Pacific Biosciences is seeking a talented Quality Control Research Associate to join our Chip NPI Systems Team. This position reports to the Manager, Senior Manufacturing Engineer, Mfg Systems. | 12/26/2022 |
| 5485 | OraSure New Brighton, MN Laboratory Technician B.Sc. or M.S. degree in Biology, Biochemistry, Molecular Biology Exp: 1+ year |
Lab Technician I will be expected to work collaboratively as part of a team. In this role, the Lab Technician I will be responsible for managing timelines, performing hands-on lab work, maintaining processing records and working in compliance with our accreditations and quality standards. | 12/26/2022 |
| 5486 | Orna Therapeutics Cambridge, MA Research Associate/Senior Research Associate, Production, Analytics B.S. in biology, biochemistry or a related discipline is required. Exp: 1+ years |
We are seeking an exceptional researcher to join our Production team as a Research Associate/Senior Research Associate. This candidate will work closely with their manager to build our internal analytical capabilities to support the advancement of our oRNA™ platform. The ideal candidate is detailed-oriented and has experience with cell-based assays and molecular biology techniques. Ownership of strong written and oral communication skills are important to be able to effectively perform within this highly cross-functional team. | 12/27/2022 |
| 5487 | Orna Therapeutics Cambridge, MA Research Associate/Senior Research Associate, RNA Production B.S. in biology, biochemistry or a related discipline required. Exp: one year |
We are seeking an exceptional Research Associate/Senior Research Associate, RNA Production to help build and maintain our proprietary RNA production process. The ideal candidate has at least a bachelor’s degree in a biological/biochemical related field with RNA handling and process development experience. They will be able to quickly learn, troubleshoot, and integrate new protocols into existing workflows; possess strong oral and written communication capabilities; demonstrate excellent collaboration & interpersonal skills; and be adept at problem solving in a fast-paced environment. | 12/27/2022 |
| 5488 | Pacira Biosciences San Diego, CA R&D Design Engineer 2 BS in Biomechanical, Mechanical, Chemical Engineering or related engineering field Exp: 1-3 years |
Primarily responsible for the development of new products and/or the enhancement of existing products. Involved in creating concepts and modeling and drafting designs utilizing 3D CAD software. Other responsibilities include drafting of design control and design history file documents, development of test plans to assess designs, and assist in the development processes. | 12/27/2022 |
| 5489 | Pacira Biosciences San Diego, CA Microbiologist 1 BS degree in Microbiology or other life science. Exp: 0 years |
The purpose of the position is to provide technical expertise in the area of pharmaceutical microbiology. The position functions in a cooperative effort to provide quality control and assurance to the operational departments involved in the manufacture of pharmaceutical products | 12/27/2022 |
| 5490 | Pacira Biosciences San Diego, CA Microbiologist 1 BS degree in Microbiology or other life science. Exp: 0 years |
The purpose of the position is to provide technical expertise in the area of pharmaceutical microbiology. The position functions in a cooperative effort to provide quality control and assurance to the operational departments involved in the manufacture of pharmaceutical products | 12/27/2022 |
| 5491 | Par Pharmaceutical Rochester, MI Chemist I (Afternoon Shift) Bachelor of Science Degree in chemistry, chemical engineering or related field with analytical chemistry coursework required. Exp: 1+ years |
The Chemist I, under direct supervision, learns and performs QC laboratory chemical analyses of raw materials, in-process materials, stability & finished products, and testing to support process validation. May participate in investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. | 12/28/2022 |
| 5492 | Parse Biosciences Seattle, WA Lab Automation Engineer Bachelor’s degree in engineering or science; preferably biology, chemistry, or related field. Exp: 1+ years |
The Lab Automation Engineer will directly contribute to the growth and success of Parse by focusing on designing and implementing creative automated solutions. As part of a growing start-up, top candidates will have the ability to design and build fully walk-a-way automation solutions that are robust and scalable. The ideal candidate can quickly identify system limitations and leverage existing technologies to engineer solutions for risk mitigations. | 12/28/2022 |
| 5493 | Fulgent Genetics Temple City , CA Lab Technician I Bachelor’s Degree in molecular biology, genetics, or related field. Exp: 1 to 4 years |
The Lab Technician I is responsible for performing clinical laboratory test procedures following standard operating (SOP) and quality assurance (QA) procedures under general supervision. The successful candidate will be a key contributor to a team committed to clinical sequencing and diagnostic test services. | 12/28/2022 |
| 5494 | Pharmaceutics International Hunt Valley, MD QA Associate Bachelor’s degree in Microbiology or Chemistry. Exp: one (1) to three (3) years |
Witness and verify the QA functions related to manufacturing of sterile product while adhering to the cGMP ICH and USP/EP/Health Canada guidelines as written -- to ensure that the day-to-day tasks of the Quality Assurance Unit supports the overall business plan while maintaining the highest quality products and ensuring the safety, identity, strength, purity, and quality that the drug is purported to possess. Perform “Line Clearance” and “Cleaning Verification” for manufacturing and packaging operations per established Standard Operating Procedures (SOPs) and Batch/Packaging and Labeling Records’ requirements. | 12/28/2022 |
| 5495 | Plex Pharma San Diego, CA RA/SRA, Biology and Protein Chemistry BS or MS in molecular and biology, protein chemistry or related field. Exp: 1-3 years |
The successful candidate will contribute to drug discovery efforts by performing cloning, expression and purification of protein drug targets, as well as assisting in assay development and characterization of compounds. | 12/28/2022 |
| 5496 | PPD Rockville, MD Associate Scientist - mRNA Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0-2 years |
To perform the following activities for Drug Product support. This list is not all-inclusive and is subject to the needs of the project, but they will be responsible for planning and executing experimental studies in the area of mRNA lipid nanoparticle production and process optimization. | 12/28/2022 |
| 5497 | PPD Boston, MA Scientist - HPLC, GC, KF Master's degree in physical sciences (Chemistry, Analytical chemistry, Organic chemistry) or engineering. Exp: 1+ year |
As a Scientist, you will use state-of-the-art technologies to perform traditional and innovative analytical techniques and Quality-by-Design principles to develop and validate the analytical tools used to ensure the safety, efficacy and quality of the customer pharmaceutical products. As a member of the Analytical Development team, you will provide project support to the drug development programs at the customer site through laboratory techniques commonly used in the analysis of pharmaceuticals such as HPLC, GC, and KF. | 12/28/2022 |
| 5498 | PPD South San Francisco, CA Associate Scientist - Organic Chemistry Bachelor's degree or master's degree in Chemistry, Process Chemistry, or Organic Chemistry. Exp: 1+ year |
As an Associate Scientist (Research Associate), you will use state-of-the-art technologies to perform high-quality research for key pharmaceutical clients across the industry. Your problem-solving skills are an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. You will join the Small Molecule team while working onsite at the client location to support various GMP/GLP campaigns. | 12/28/2022 |
| 5499 | PPD Fremont, CA Engineer/Scientist I, QC BS/BA in Chemistry, Biochemistry, or Bioscience required. Exp: 1+ years |
Using standard operating procedures (SOP) and good manufacturing practices (GMP), the Engineer/Scientist I will perform intermediate and final release testing of filled components and finished goods kits. The Engineer/Scientist I will be responsible for all aspects of laboratory testing, such as sample receipt, data generation, product verification, data analysis and summarization, instrument operation, and all other QC lab supporting activities. | 12/29/2022 |
| 5500 | PPD Florence, SC Analytical R&D Scientist I Bachelor’s degree in chemistry or related field required. Exp: 1-2 years |
The Scientist I conducts laboratory work as necessary to assure that products are tested per operating procedures. Ensure that work is carried out in an efficient and safe manner. Utilizes judgment in making adaptation and modifications on all assignments. Provides routine analyses in an analytical chemistry laboratory following standard practices. Performs analytical methods as assigned for testing on raw materials, samples, stability, production intermediates, and active pharmaceutical ingredients, including method development and qualification activities. Supports internal development and/or manufacturing operations. Makes detailed observations and reviews, documents, and communicates test results | 12/29/2022 |
| 5501 | Principia Biopharma Framingham, MA Manufacturing Associate - 2nd Shift Bachelor’s Degree in Biology, Chemistry, Biochemistry, or Chemical Engineering. Exp: 1-3 years |
As part of the Sanofi Genomic Medicine Unit organization in Framingham, the Cell Therapy Manufacturing Suite (CTMS) is responsible to support manufacturing of cutting-edge biologic drug substance material to support clinical candidate programs. The CTMS group operates in clean-room production suites under cGMP conditions to produce cell therapy products suitable for use in First in Human stage clinical trials. CTMS also interacts closely with the Quality Assurance (QA), Bioprocess Engineering, Validation, and other groups to ensure cGMPs and manufacturing schedules are maintained. Operations’ main functions are the execution of manufacturing campaigns, leading deviation investigations and managing CAPA implementation, partnering with direct manufacturing staff for enhancing and improving the manufacturing instruction set, overseeing and supporting manufacturing’s training program, and identifying and managing continuous improvement initiatives. This role is second shift: Sunday to Wednesday 3:30PM-2AM or Wednesday to Saturday 3:30PM-2AM | 12/29/2022 |
| 5502 | Principia Biopharma Swiftwater, PA Production Technician - Vaccines Associate or Bachelors' degree in Life Sciences or other relevant fields of study. Exp: no experience |
Performs production in accordance with volume fluctuation, business need, and effective procedures. Must be flexible to ensure staffing for changing business volume and needs. Works with Senior Technicians, leads, and managers to ensure operational area is running as intended to meet all operational goals. Must attend shift change daily to ensure preparedness for workday. Completes Real Time SAP transactions on all aspects of Inventory Management. Obtains and Maintains access to necessary systems as needed (SAP, RT Reports, Gibralter, HMI, SCADA access, Virtual Standards, etc.) | 12/29/2022 |
| 5503 | Principia Biopharma Swiftwater, PA Production Technician, Swiftwater, Pennsylvania - Vaccines Associate or Bachelors' degree in Life Sciences or other relevant fields of study. Exp: no experience |
You are a detail-oriented person who thrives in a fast-paced team environment. The production technician is the “heartbeat” of the vaccine manufacturing and is primarily responsible for the high quality and efficient production of our vaccines in accordance to current good manufacturing practices (cGMP) for all relevant regulatory agencies (e.g. FDA). Like all production positions at the Company, this position may require to be moved or temporarily flexed to another department/location within the Swiftwater site due to business needs. This is a 40-hour work week. | 12/29/2022 |
| 5504 | Principia Biopharma Swiftwater, PA Fill LL-2 - Vaccines Associate or Bachelors' degree in Life Sciences or other relevant fields of study. Exp: no experience |
You are a detail-oriented person who thrives in a fast-paced team environment. The production technician is the “heartbeat” of the vaccine manufacturing and is primarily responsible for the high quality and efficient production of our vaccines in accordance with current good manufacturing practices (cGMP) for all relevant regulatory agencies (e.g., FDA). Like all production positions at the Company, this position may require to be moved or temporarily flexed to another department/location within the Swiftwater site due to business needs. This is a 40-hour work week. | 12/30/2022 |
| 5505 | Principia Biopharma Swiftwater, PA Fill LL-3 - Vaccines Bachelor’s degree Exp: 1+ years |
Responsible for working inside the fill area. Performs production in accordance with volume fluctuation, business need, and effective procedures. | 12/30/2022 |
| 5506 | Principia Biopharma Swiftwater, PA Associate Scientist Manufacturing Technology Bachelor in Basic Sciences, Pharmacy, Chemical Engineering or Mechanical Engineering Exp: 1-3 years |
This position of Industrial Affairs Associate Engineer I Scientist, within the Manufacturing Technology (MTech) function of Industrial Affairs, performs activities supporting the development, validation and continuous improvement of visual inspection processes for Drug Products. The mission of the MTech function is to deliver robust and efficient processes & testing with associated knowledge to transfer to Manufacturing & QC. The Mtech function also provides daily support to manufacturing and QC toward industrial performance excellence. | 12/30/2022 |
| 5507 | ProteinSimple Austin, TX Research Associate Bachelor’s degree in biology, chemistry, biomedical engineering, or related field is required. Exp: 1-3 years |
Asuragen is seeking an outstanding BSc-level scientist to join our Research group. This is a full time position focused on developing innovative nucleic acid or protein-based technologies. This role will support new product initiatives to enable novel, multiplexed-PCR technologies that can resolve multiple classes of DNA/RNA markers or proteomics through integration of reagents, instrumentation, analysis algorithms and software. Platforms used in our laboratory include quantitative real-time PCR, digital PCR, capillary electrophoresis, next-generation and long-range sequencing. | 12/30/2022 |
| 5508 | ProteinSimple Minneapolis, MN Research Associate, Mammalian Cell Culture Bachelor’s degree in a biological science. Exp: 0 to 2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for recombinant protein production, media and supplement preparation, and additional duties as assigned. This position requires a Tuesday through Saturday workweek. | 12/30/2022 |
| 5509 | ProteinSimple Minneapolis, MN Research Associate, Array Manufacturing Bachelor’s degree in chemistry, biological sciences or equivalent. Exp: 0 to 2 years |
We are seeking a Research Associate for Bio-Techne’s Proteome Array Manufacturing department at our Minneapolis Headquarters. Our group supports manufacturing proteome array panels and cell isolation kits used in academic research, pharmaceutical research, and all facets of biological science including oncology, neurodegenerative diseases, stem cell research, developmental biology, etc. This individual will be trained on and work with array printing robot for microarray and perform benchtop in-process QC testing for array components. This individual will also have opportunities to collaborate with many different departments including Planning, QC, & Conjugation to support the manufacturing processes of our products. This position provides a potential for growth and career advancement within the company. | 12/30/2022 |
| 5510 | ProteinSimple Minneapolis, MN Quality Technician MLT/MLS degree, Bachelor’s degree in Biology, or related field of study. Exp: 0-1 year |
This position will require setup, maintenance, troubleshooting, and operation of QC hematology analyzers. This position will require monitoring instrument performance throughout the QC process and troubleshooting the instrument when necessary. This position will test hematology products for homogeneity during the bottling process by following established methods. The expectation for this position is to setup and QC product on 50% of the laboratory instruments and troubleshoot as necessary. You will assist the QC Laboratory Manager/Supervisor with releasing products to bottle and ship, proofing labels and assay sheets. You will serve as a member of the Technical Service team by rotating through our Technical Service Department and responding to customer inquiries and complaints with the assistance of senior members of the department. This position will adhere to safety regulations. Perform additional duties as assigned. | 12/30/2022 |
| 5511 | ProteinSimple Minneapolis, MN Research Associate, Microbiology QC Bachelor’s degree in Microbiology or a related scientific field or equivalent. Exp: up to 3 years |
The responsibilities of this position are to participate in the Microbiology QC testing and reporting procedures: set up, read, and report the microbial QC bioburden and sterility testing of various sample types using culture methods that include direct plating, broth inoculation, and membrane filtration. Performance of environmental monitoring for viable microbes, particle counts, and WFI/deionized water testing, reading, and reporting. Assist with efficacy and validation testing, new procedure development, new equipment IQ/OQ and calibrations. Perform general lab duties, assist with sanitization of clean rooms, and additional duties as assigned. | 12/30/2022 |
| 5512 | Protomer Technologies Pasadena, CA Chemist / Biochemist Undergraduate degree in chemistry, biochemistry, chemical engineering with working knowledge of standard biochemistry or chemistry lab techniques. Exp: 1+ years |
The ideal candidate will have a bachelor’s or master’s degree in chemistry, chemical engineering, biochemistry, biology, or a related field, as well as in-depth understanding of basic biochemistry and chemistry techniques and experience with development, validation, and implementation of experiments in a biomedical research setting. The applicant must be a fast-learning, task-oriented, and self-motivated person who can perform detailed work with minimal supervision. A requirement of this role is to work well as a team player in a fast-paced research setting. The applicant will be responsible for assisting Protomer’s senior chemists with synthesis, bioconjugation, purification, and characterization of compounds of interest. The successful candidate will actively participate and present in team meetings and is expected to contribute to the team’s progress and success. | 12/30/2022 |
| 5513 | Protomer Technologies Branchburg, NJ Research Associate-Quality Control (QC) Bioassay Master's Degree in a science related field (e.g. Biology, Biochemistry, etc.). Exp: 1 year |
Conduct routine and non-routine analyses of in-process materials, finished goods and stability samples by appropriate biochemical methods as assigned by supervisor. Perform routine QC responsibilities as needed. Apply acceptable cGMP practices during execution of all work tasks. Work independently with moderate supervisory guidance. | 12/30/2022 |
| 5514 | PsychoGenics Paramus, NJ Research Associate 1 – Surgery/Neuroscience Bachelor's degree in life sciences, neuroscience, or psychology. Exp: 1+ years |
We are looking for a highly motivated Research Associate in surgery. The successful candidate will work in a team of scientists and researchers supporting the preclinical studies using rodent models and tests. The primary responsibilities of the candidate will include but are not limited to conducting preclinical research using various surgical procedures primarily in the area of pain, animal disease model, and other drug discovery assays as needed. The candidate will be responsible for surgeries, tissue collection and drug administration, proper execution of experiments, and preliminary data analysis. The candidate must be capable of working across teams and independently. | 12/30/2022 |
| 5515 | PsychoGenics Paramus, NJ Research Associate - Neuropharmacology Bachelors or Masters degree in the biological sciences, neuroscience, or related field. Exp: 1-3 years |
We are looking for a highly motivated Research Associate in neurodegenerative disorders. The successful candidate will work in a team of scientists and researchers supporting preclinical studies using rodent models. The primary responsibilities of the candidate will include, but are not limited to, dosing animals, conducting behavioral assessments for neurodegenerative disorders, and dissection and tissue collection. The candidate will be responsible for coordinating studies and the proper execution of experiments. The candidate must be capable of working both across teams and independently. | 12/30/2022 |
| 5516 | PTC Therapeutics Pennington, NJ Associate Scientist I, Analytical Development (Biological Assays) - Gene Therapy Master’s degree in biology, molecular biology, virology, biochemistry or related discipline. Exp: 0 to 3 years |
The Associate Scientist I, Analytical Development - Gene Therapy is responsible for the execution and analysis of well-established, routine assays (including, but not limited to, qPCR, cell-based and immunoassays) supporting the gene therapy analytical development organization. S/He is also responsible for communicating assay results to his/her supervisor. | 12/30/2022 |
| 5517 | PTC Therapeutics Bridgewater, NJ Associate Scientist I, Pharmacology Master’s degree in a scientific discipline. Exp: 0- 2 years |
The Associate Scientist I, Pharmacology is responsible for performing scientific experiments that contribute to research and drug discovery activities at PTC in PK/PD, inflammation, oncology and/or neurological diseases area. The incumbent, Pharmacology is also responsible for communicating experimental results to his/her supervisor and the project team. | 12/30/2022 |
| 5518 | PTC Therapeutics Mountain View, CA Research Associate II, Biology Master's Degree in a scientific discipline. Exp: 0- 2 years |
The Research Associate II, Biology is responsible for performing scientific experiments that contribute to research and drug discovery activities at PTC. This position assists in the conduct of early-stage research, the goal of which is the identification of New Chemical Entities (NCEs), as well as the advancement of research programs from the identification of screening hits to advanced lead optimization. The incumbent is also responsible for communicating experimental results to his/her supervisor and the project team. | 12/30/2022 |
| 5519 | PTC Therapeutics Bridgewater, NJ Associate Scientist I, Biology ( Neuroscience) Master’s degree in a biology scientific discipline. Exp: 0-2 years |
The Associate Scientist I, Biology (Neuroscience) is responsible for performing scientific experiments that contribute to research and drug discovery in the area of neuroscience. This position assists in conducting preclinical research collecting data from brain tissue of in-vivo rodent models with a concentration on the central nervous system. The candidate is responsible for generating, interpreting, and reporting data in support of novel therapeutic discovery. | 12/30/2022 |
| 5520 | DPT Laboratories San Antonio, TX Associate Scientist QC Method Validations BS in Chemistry, Biology or Biochemistry (with solid chemistry knowledge) from a four-year college or university is required. Exp: 0 – 3 years |
Perform analytical method development / validation and sample analysis. Typically, the development and/or validation will be conducted according to instructions in a protocol. The associate scientist will work with supervision from the Group Leader and/or Senior Scientist. Review the data generated during the development / validation and determine if the acceptance criteria in the protocol is being met. The associate scientist will report any failures to the Group Leader. Write standard methods of analysis. Write technical reports for method development / validation work. Write and review analytical test methods, and reports. | 12/22/2022 |
| 5521 | DPT Laboratories Morgantown, WV Chemist II Bachelor's degree (or equivalent) Exp: 0-2 years |
Perform pharmaceutical testing including, but not limited to, HPLC, GC, TLC, UV, dissolution, and IR spectroscopy. Develop and validate analytical test methods for pharmaceutical products. Critically evaluate and audit data. Write technical analytical reports and procedures. | 12/22/2022 |
| 5522 | NanoString Bothell, WA Quality Assurance Associate I Bachelor's degree in engineering, science, business, or liberal arts Exp: 0-3 years |
As a Quality Assurance Associate I, you will have a strong desire to be part of our Quality Team and assist in the administration of the Document Control and Quality Management System (QMS). As well as perform Quality Assurance (QA) product release. You will possess strong attention to detail and have a collaborative and team-oriented disposition. | 12/22/2022 |
| 5523 | Nanosyn Santa Clara, CA Associate Research Scientist B.S. in Chemistry, Biochemistry or other relevant discipline Exp: 0-2 years |
Develop new methods for the synthesis of organic molecules and prepare intermediates for the synthesis of these molecules. Apply modern techniques of organic synthesis including a variety of organic reactions at several scales, inert atmosphere techniques, thin-layer chromatography, NMR, LC-MS, HPLC, MS, flash chromatography, recrystallization, distillation, etc. | 12/22/2022 |
| 5524 | Nanosyn Santa Clara, CA Research Associate / Screening and Compound Profiling BS in Biology, Biochemistry or other relevant discipline Exp: 0-2 years |
We are currently seeking a highly motivated screening and compound profiling research associate to join our biology department in Santa Clara, CA. The candidate will play a key role in the organization by being responsible for the planning and timely execution of in vitro biochemical and cell-based assays for Nanosyn’s screening and profiling services. He/She will be responsible for consistently generating high quality data and meeting agreed upon timelines. Applicants must have a strong focus on quality and attention to detail, have the ability to work on multiple projects simultaneously, and be productive both independently and as part of a team. The ideal candidate should have good organizational skills, possess good problem solving, communication and interpersonal skills and to adapt rapidly to new challenges. | 12/22/2022 |
| 5525 | Natera San Carlos, CA Laboratory Associate: New College Graduate (2022 - 2023) BS/BA in a biological science or a related field Exp: new graduates |
Assists in analyzing specimens and maintains equipment in good operating condition. | 12/22/2022 |
| 5526 | Natera Austin, TX Laboratory Associate: New College Graduate (2022 - 2023) BS/BA in a biological science or a related field Exp: new graduates |
Assists in analyzing specimens and maintains equipment in good operating condition. | 12/22/2022 |
| 5527 | Natera Austin, TX Research Technician BS/BA in a biological science or equivalent required Exp: 1-2 years |
The Research Technician performs routine laboratory research and development services. Works with a multidisciplinary team. Under nominal direction, performs a variety of basic and general laboratory research and sample management tasks determined by the field and scope of the research project. | 12/22/2022 |
| 5528 | Natera Austin, TX Medical Laboratory Scientist BS/BA degree in Medical Technology, Biological Sciences, or a related field Exp: 0-9 yrs |
Natera is currently seeking a licensed Medical Laboratory Scientist to analyze specimens and maintains equipment in good operating condition. | 12/22/2022 |
| 5529 | Natera Austin, TX Medical Laboratory Scientist ( Recent Grads) BS/BA degree in Medical Technology, Biological Sciences, or a related field Exp: 0-9 yrs |
Natera is currently seeking a licensed Medical Laboratory Scientist to analyze specimens and maintains equipment in good operating condition. | 12/22/2022 |
| 5530 | Natera Austin, TX Instrument Support Engineer BS/BA in a biological science/biomedical engineering, similar field of study. Exp: 1 years |
The Instrument Support Engineer is responsible for the service and support of laboratory equipment and instrumentation utilized in the Operations laboratory. The scope of support includes installation, calibration, maintenance, and repair of both simple (e.g., plate sealers) and complex (e.g., liquid handling robotics) instrumentation in the laboratory. The Instrument Service Engineer will be the primary point of contact for production lab personnel when equipment and instruments are not operating or not meeting operational specifications. | 12/22/2022 |
| 5531 | NorthEast BioLab Hamden, CT Associate Scientist, Central Laboratory Services B.S. in Physiological Science, Epidemiology, Microbiology, Immunology, Genetics, Biology, Molecular Biology, Cell Biology, Biotechnology, Biochemistry Exp: Entry Level |
Gain an overall understanding of drug development and maintenance of the full chain of sample custody for regulatory compliance Support implementation of Laboratory Information management System (Watson LIMS) for sample management and storage Sample management and reconciliation, kit preparation and verification, and document preparation related to biological sample collection, storage, and shipment for clinical trials Streamline inventory management, consumable ordering, and other documentation requests for Quality Assurance Unit Help maintain ultra-low temperature (ULT) freezers and refrigerators and associated electronic logs and records Learn bioanalytical techniques for the analysis of drug and biomarkers in biological matrices | 12/22/2022 |
| 5532 | Nektar Therapeutics Huntsville, AL Process Technician I / II (Pharmaceutical Manufacturing) For Process technician I: BS Degree in Chemistry, Biochemistry, Chemical Engineering preferred, or other science related proferred. Exp: 0-2 years |
Nektar has an exciting opportunity for a Process Technician I / II to join the Manufacturing team in our Huntsville, AL office. Day Shift: M-Th 6am - 6pm, F 6am to early afternoon. | 12/22/2022 |
| 5533 | Neos Therapeutics Grand Prairie, TX Chemist I Bachelor's degree in a science-related field or equivalent experience Exp: 1 year |
The QC Chemist I position plays a key role in the operation of the QC Laboratory. This chemist will be responsible for the timely analysis of a wide variety of samples. The QC Chemist I provide services for other departments (Production, R&D, QA, Engineering), all while operating in a state of compliance with current Good Manufacturing Practices (cGMPs). | 12/22/2022 |
| 5534 | Nephron Pharmaceuticals West Columbia, SC Microbiology Lead Environmental Monitoring Technician Bachelor’s degree preferred. Exp: 1 – 2 years |
Provides oversight and support of the environmental monitoring (EM) program during production operations. Assists Microbiology department management with environmental excursion investigations and non-conformance reports. Performs environmental monitoring activities as necessary. Assists with additional work duties or responsibilities as evident or required. | 12/22/2022 |
| 5535 | Nephron Pharmaceuticals West Columbia, SC QC Microbiology Laboratory Technician Master’s degree in Biology, Microbiology, or Life Sciences preferred. Exp: 1 year |
· Perform microbiology department related tests according to USP methods and established procedures that follow cGMP guidelines and demonstrate outstanding aseptic techniques. Microbiology test methods include the following: bioburden, bacterial endotoxins, sterility, particulate matter, microbial identification, growth promotion, and vacuum decay container closure tests. · Assists in the receipt, storage, organization, and disposal of laboratory samples while ensuring compliance with FDA and DEA regulations. · Additional work duties or responsibilities as evident or required.· Perform microbiology department related tests according to USP methods and established procedures that follow cGMP guidelines and demonstrate outstanding aseptic techniques. | 12/22/2022 |
| 5536 | Nephron Pharmaceuticals West Columbia, SC Microbiology R&D Analyst I Master’s Degree in Microbiology or other science-related field Exp: 1 - 3 years |
Performs research and develops projects for both established and new products, including, but not limited to, microbiological test method validation/transfer/verification, procedures, investigations, and other non-specified projects or initiatives. Plans, organizes, and manages resources on method validation projects to assure technical quality and schedule adherence. Performs other duties as assigned or apparent. Works with different microbiological techniques and equipment, including but not limited to gram stain, turbidimetric endotoxin testing, liquid particle counter, isolator, bioburden, filtration analysis, sterility testing, aseptic process simulation, and MALDI-TOF. Performs different microbiological tests for R&D Microbiology and QC Microbiology, as needed; also understands and performs routine investigations related to Environmental Monitoring and laboratory testing. Works in a GMP environment and responsible for generating cGMP data. | 12/22/2022 |
| 5537 | Nephron Pharmaceuticals West Columbia, SC Quality Systems Scientific Specialist Tier I Bachelor’s degree preferred. Exp: 1-2 years |
Responsible for ensuring compliance with all State and Federal regulatory bodies as it pertains to the completion of Annual Product Review (APR) for all Nephron Pharmaceuticals Corporation (NPC) and Nephron 503B Outsourcing Facility (503B) drug products. Performs reviews of Standard Operating Procedures (SOP) and other formal, controlled documents for approval of any updates needed. Performs other duties as assigned or apparent. | 12/22/2022 |
| 5538 | Nephron Pharmaceuticals West Columbia, SC Analytical Chemist I - Second Shift (Sun. - Thurs. - 2:00pm to 11:00pm) BS or MS in Chemistry, Biochemistry or a related field required. Exp: 0-3 years |
• Support quality control testing and research and development activities as needed. • Assists with additional work duties or responsibilities as evident or required. • Performs other duties as assigned or apparent. • Relies on instructions and pre-established guidelines to perform job functions. • Works under immediate supervision. | 12/22/2022 |
| 5539 | Nephron Pharmaceuticals West Columbia, SC Analytical Chemist I - First Shift (Mon. - Fri. - 8:00am to 5:00pm) BS or MS in Chemistry, Biochemistry or a related field required. Exp: 0-3 years |
• Support quality control testing and research and development activities as needed. • Assists with additional work duties or responsibilities as evident or required. • Performs other duties as assigned or apparent. • Relies on instructions and pre-established guidelines to perform job functions. | 12/22/2022 |
| 5540 | Nostrum Laboratories Bryan, OH Chemist I Bachelor’s Degree. Exp: 0 - 4 years’ |
Responsible for development and validation of analytical methods in support of product development and IND/NDA/ANDA filings. Perform routine wet chemical and instrumental analysis on raw materials, in-process, finished and stability products. Accurately compiles and reports data. Gather, compile and compose documents needed for regulatory submissions. | 12/22/2022 |
| 5541 | Novartis Cambridge, MA BS/MS Research Scientist, Oncology Drug Discovery - Biotherapeutics MS Exp: 0-4 years |
We are seeking a highly passionate and motivated research scientist to join our team at Novartis Oncology Biotherapeutics in Cambridge, MA. This position is ideal for someone who is creative, highly collaborative, result-oriented and wishes to combine their curiosity about oncology, cancer immunology and drug discovery to save patients’ lives. In this role, you will have the opportunities to contribute to exploratory and innovative biotherapeutic drug discovery for cancer using a variety of different assays to independently support research in this area. The successful candidate will become a crucial part of a dynamic and multidisciplinary group to interact with other functional groups and to understand the process of preclinical drug discovery, that will eventually transform the lives of cancer patients. | 12/22/2022 |
| 5542 | Novartis Cambridge, MA Research Scientist, Protein Engineering MS in biochemistry, molecular biology or related field. Exp: 0+ years |
We are looking for a passionate Research Scientist to join the team in Cambridge, MA. In this role, you will help to advance our diverse programs in NBC biologics pipeline and accelerate the discovery process. You will mainly work in lab to support all projects cross the portfolio in the protein engineering function by contributing to protein expression, purification, and characterization. | 12/22/2022 |
| 5543 | Novartis San Francisco, CA Research Scientist I, NITD Pharmacology Bachelor’s degree (B.A./B.S.) in biomedical or life sciences field preferred. Exp: 0-2 years |
The NITD Pharmacology group provides high quality in vivo research work and support to enable drug discovery research and development. We are looking for a Research Scientist I to coordinate and run in vivo research studies and projects to support the diverse and exciting project portfolio at NITD. The candidate should be action-oriented, skilled in experimental animal work, and possess a strong scientific background in order to plan, design, coordinate and perform in vivo experiments with high technical and ethical standards. The role will require an ability to work independently as well as in close collaboration with other research scientists. | 12/22/2022 |
| 5544 | Novartis Cambridge, MA Research Scientist, AAV Cell & Gene Therapy B.S in in Molecular/Cell Biology, Biochemistry or related field. Exp: 1+ years |
We are seeking a highly motivated scientist to join the Biotherapeutic Engineering and Gene Therapy (BEGT) group within NBC in Cambridge, Massachusetts. The BEGT group drives a diverse portfolio of modalities including therapeutic proteins, multi-specific antibodies, CAR-T, RNA therapeutics and AAV. Through innovative and rational protein design as well as cell and viral engineering, the BEGT group works collaboratively within NIBR to broaden the use of biologics into therapeutic applications where conventional antibodies have limitations. | 12/23/2022 |
| 5545 | Novartis Morris Plains, NJ QC Associate Scientist (PM Shift) Bachelor’s degree in chemistry, biochemistry, microbiology or other related science. MS preferred. Exp: 1 year |
Under general direction, the QC Associate Scientist will perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay and raw materials, as appropriate). | 12/23/2022 |
| 5546 | Novavax Gaithersburg, MD Laboratory Technician, Formulation - NanoFlu (Contractor) bachelor diploma Exp: 0 – 2 years’ |
We are seeking a Lab Technician to join our Formulation Department – NanoFlu, who can fulfill the job requirements listed below. This position is lab-based and will support formulation scientists in day-to-day laboratory activities, including analytical testing of samples and buffer preparation and testing. The Lab Technician is also responsible for maintaining laboratory inventory and upkeep. This position is lab-based and will be located at our Gaithersburg, MD facility. | 12/23/2022 |
| 5547 | Novavax Gaithersburg, MD Specialist I, QA/Batch Release Project Coordinator BS Exp: No experience |
We are seeking a Quality Specialist I to join our Quality Assurance as batch release and project coordinator in Gaithersburg, MD. The specialist will be responsible for support of GMP compliance with a focus on project coordination between the various QA/QC groups. The candidate will provide project coordination support, ensure organizational alignment of the QA/QC teams, and ensure all documents and the data is accurate, provide status update on all on going projects and programs. This position will require periodic weekend/evening work and travel. | 12/23/2022 |
| 5548 | Novavax Gaithersburg, MD Associate II - Analytical Development, Physicochemical, Early-Stage (Contractor) Master’s degree Exp: 1 year |
We are currently seeking an Associate II - Analytical Development (Physicochemical, Early-Stage). This contractor role is responsible for contributing to the method development, qualification, and technology transfer for analytical methods to support Early-Stage programs, including Influenza, RSV, and others. The qualified individual will bring experience in relevant analytical technologies, such as SDS-PAGE, UV-Vis, DLS, RP-HPLC, and IEX-HPLC. The position will perform in-process testing, as needed, in order to support the Process Development, Formulation Development, and Manufacturing teams, in addition to method development and qualification. This position will be located at our Gaithersburg, MD facility | 12/23/2022 |
| 5549 | NovoBiotic Pharmaceuticals Cambridge, MA Associate Scientist - Microbiologist B.S. or M.S. in Biology/Microbiology Exp: 0 to 5 years |
We are currently seeking to hire microbiologists with 0 to 5 years of experience. The successful applicant will perform microbiology lab work and data analysis to discover previously unculturable microorganisms from soil and marine environments and their identification by molecular taxonomy methods. Additional tasks will include detection of antibiotic production from these organisms and in vitro characterization of their properties, such as spectrum of activity, mechanism of action, resistance development and cytotoxicity | 12/23/2022 |
| 5550 | Novo Nordisk West Lebanon, NH Cell Therapy Associate Master’s Degree in Cell Biology, Molecular Biology or a closely related field preferred. Exp: one (1) year |
This position has the responsibility of working with senior level Scientists and manufacturing associates to execute process development, scale-up, tech transfers, and validation studies in support of manufacturing or analytics. Additionally, the role will necessitate experimental troubleshooting, GMP documentation and laboratory investigations. The position will require understanding the underlying science of the process and manufacturing equipment, or assay methods and instruments. | 12/23/2022 |
| 5551 | Noxilizer Hanover, MD Research and Development Laboratory Scientist Bachelor’s degree in Biology, Biotechnology, Biomedical Engineer, Material Science or related field preferred. Exp: 1 year |
The R&D Lab Scientist is responsible for performing, documenting and reporting microbiological sterilization studies for Noxilizer’s customers. Noxilizer’s customers range from Fortune 500 pharmaceutical, biotech and medical device companies to start-ups that are in the US, Europe and Asia. These studies are the first critical step in the customer’s evaluation of nitrogen dioxide sterilization and their product, as well as an important revenue-generating area for the company. The R&D Laboratory Scientist will join a high-performing team of experts to solve sterilization challenges while they grow their skills for future career opportunities. | 12/23/2022 |
| 5552 | NuProbe Houston, TX Technician I/II (BD/Services) BA/BS, MA/MS in Biology, Biochemistry, or related field Exp: 1 – 3 years |
The Technician I/II will execute most of the Research & Development protocol activity which is vital to the success of the company. This position handles sensitive data and comes with a high degree of trust. | 12/23/2022 |
| 5553 | NuProbe Houston, TX Technician I (Innovation) BA/BS or higher in Biology, Biochemistry, Biotechnology, or a related field Exp: 0 – 3 years |
The Research Technician I – Innovation Department executes most of the research & development protocol activity which is vital to the success of the company. This position handles sensitive data and comes with a high degree of trust. | 12/23/2022 |
| 5554 | Ocean Ridge Biosciences Exton, PA QA Specialist-GLP/BIO B.S. degree in related scientific discipline Exp: >1 years |
Implement, maintain and enhance quality procedures and systems to ensure compliance with US FDA, OECD, and ICH regulatory requirements including 21 CFR Part 58, 21 CFR Part 11, 21 CFR Part 320, and other relevant guidances and publications. One of our groups also works to 40 CFR part 160. Conduct QA audits of BIO laboratories and functions including but not limited to: ongoing process, data review audits, technical report, and study independent facility / process. Provide input to method, equipment, computer validation programs. | 12/23/2022 |
| 5555 | Ocean Ridge Biosciences Exton, PA Associate Scientist, Pharmaceutical Analysis-Microbiology B.S. in Biology or related discipline Exp: 1-2 years |
Performs routine microbiology sample analysis (Bioburden, Endotoxin, Environmental Monitoring, Sterility, etc.) and a variety of tasks to support product development, ensuring agreed timelines | 12/23/2022 |
| 5556 | Ocean Ridge Biosciences Hayward, CA Research Assistant-ADME BS in biology, biochemistry and other related fields. Exp: 0-3 years |
We are looking for a highly-motivated Research Assistant to develop and conduct biochemical and cellular assays to evaluate potential therapeutics. Experience in cell line development, ELISA, PBMC biomarker, cell culture, cellular assays, gene expression is desirable. Prior experience in ADME assays including metabolite stability, drug transporter, CYP450, PPB and measurements of physicochemical properties is preferred. The candidate needs to be proficient in assay design, trouble-shooting, data analysis and working with 96-w & 384-w plate-based assays. The candidate needs to have a good understanding of drug discovery processes and experience in a discovery project is preferred. This position requires working with an interdisciplinary team of DMPK scientists, analytical chemists and pharmacologists. | 12/23/2022 |
| 5557 | Ocean Ridge Biosciences Concord, OH Entry Level Lab Chemist B.S. in a chemistry or related field. Exp: Entry Level |
This position is for an entry level lab chemist. The ideal candidate will help support studies of preclinical drug development in a GLP environment. | 12/23/2022 |
| 5558 | Ocean Ridge Biosciences Exton, PA Associate QC Specialist Bachelor Degree or Master Degree in Chemistry, Biochemistry or other scientific field Exp: 0-2 years |
Review of Biomarker bioanalytical data (notebook documentation, raw data, and LIMS data) for accuracy, consistency, and completeness to ensure compliance with SOPs and GLP. Review method development/qualification/validation reports and sample analysis reports including text and data for accuracy and consistency. Preparation of bioanalytical test result data tables for clinical testing reports. Review of client data transfer specifications. Prepare and transmit client data transfer tables. | 12/23/2022 |
| 5559 | Ocean Ridge Biosciences Hayward, CA Research Associate M.S. degree in related scientific discipline Exp: 0-3 years |
1) Perform Watson design according to Study Protocols 2) Conduct basic method development and validation studies. 3) Ability to troubleshoot and solve basic technical and instrumental issues. 4) Conducts and documents work in a regulated environment. 5) Reviews the data package and notebooks for junior chemists 6)Writing up analytical methods, protocols, and reports under supervision 7) Perform project communication with client, study director, and project management team under supervision | 12/23/2022 |
| 5560 | Lucigen Gaithersburg, MD Research Associate I – Manufacturing (47370) Bachelor’s degree in Biochemistry or Molecular Biology or a related field Exp: one year |
The Research Associate I position will advance LGC Clinical Diagnostics Division purpose of understanding disease by supporting the manufacture of precision diagnostic products. Support includes independently performing routine and non-routine applications of cellular/molecular genetic technology to quantitate and manipulate genetic material all under GLP/GMP. | 12/12/2022 |
| 5561 | Lucigen Cumberland, ME Manufacturing Chemist I (47324) Bachelors degree in life science field or other related science or medical curriculum Exp: no experience |
The Manufacturing Chemist I fulfils the essential role of preparing reagents, buffers, stocks, and other solutions using established procedures within the operations laboratory. They will use general laboratory equipment and techniques to perform these tasks under both direct and indirect supervision. They are expected to perform routine analysis and interpretation of test results against established acceptance criteria with limited judgment. | 12/12/2022 |
| 5562 | Lucigen Petaluma, CA Therapeutic Production Chemist I - Day Shift (46932) Bachelors of Science in a relevant STEM field Exp: 1 or more years’ |
The Therapeutic Production Chemist I perform routine oligonucleotide manufacturing processes in the LGC Axolabs Petaluma Therapeutic GMP suite. Processes include: synthesis, cleavage and deprotection, purification, desalting, and lyophlization of oligonucleotides, | 12/12/2022 |
| 5563 | Lucigen Charleston, SC QC Chemist (42600) Bachelor of Science in chemistry degree or equivalent is preferred Exp: one-year |
This is an entry QC chemist position where one is responsible to make check standards, routine instrument maintenance and operation of GC/MS, GC/FID, HPLC, and UHPLC/MS, validating manufactured products in a timely manner. Attention to detail, teamwork, the ability to thrive in a fast-paced work environment and organizational skills are necessary to excel in this position. | 12/12/2022 |
| 5564 | Lucigen Petaluma, CA Therapeutic Production Technician I - Entry Level- Day Shift (47172) Bachelors degree preferred with a Science background Exp: 1+ years' |
The Therapeutic Production Technician will support oligonucleotide manufacturing processes in the LGC Axolabs Petaluma Therapeutic GMP suite. Activities include: daily calibration of instruments, stocking materials, cleaning and maintaining labware. | 12/12/2022 |
| 5565 | Lucigen Petaluma, CA Therapeutic Production Chemist - Night Shift (47170) Bachelor of Science in a relevant STEM field is required. Exp: 1+ years' |
The Therapeutic Production Chemist will perform routine oligonucleotide manufacturing processes in the LGC Axolabs Petaluma Therapeutic GMP suite. Processes include: synthesis, cleavage and deprotection, purification, desalting, and lyophilization of oligonucleotides. | 12/12/2022 |
| 5566 | Lung Biotechnology Research Triangle Park, NC Bioprocess Associate I/II - Cell Biology, Bioprocess Development Bachelor’s Degree in Arts/Sciences (BA/BS) in biology, cell and molecular biology, biomedical sciences, biomedical engineering, biomanufacturing, or a Exp: Bioprocess Associate I: 1+ years |
Conduct and assist in research efforts to develop tissue-based regenerative medicine products for the treatment of pulmonary hypertension and other lung diseases. | 12/12/2022 |
| 5567 | Lung Biotechnology Manchester, NH Research Associate I – Cellularization Bachelor’s Degree in Arts/Sciences (BA/BS) in Cellular Biology, Developmental Biology, or Biomedical Engineering or related field Exp: 1+ years |
The Research Associate I - Cellularization (OMG) will support the development and characterization of bioinks for 3D printing scaffolds for lung tissue engineering. They will design and print 3D diagnostic models to test bionks for compatibility with different lung cell types. | 12/12/2022 |
| 5568 | Lung Biotechnology Manchester, NH Associate Process Engineer/ Process Engineer, Biomaterials Bachelor’s Degree in Arts/Sciences (BA/BS) in materials science, chemistry, chemical, mechanical or biomedical engineering (or equivalent) Exp: 1+ years |
The Associate Process Engineer, Biomaterials (OMG) will be responsible for scaling up and experimenting with large batches of ink to support process and product feasibility goals. This position will also be responsible for periodic quality control (QC) testing. | 12/12/2022 |
| 5569 | Lykan Bioscience Hopkinton, MA QC Analyst, Microbiology Certificate in Biotechnology or Bachelor's degree in scientific discipline preferred Exp: 0-7+ years' |
The Quality Control Analyst environmental monitoring will be responsible for collection of environmental samples in clean room areas to support manufacturing operations, sample management activities, and testing of cell therapy in-process, release and stability product samples. He/she will be responsible for reporting of data and writing/revising standard operating procedures (SOPs). He/she may support equipment onboarding and qualification as well as test method qualification in compliance with all applicable quality systems and current cGMPs. | 12/12/2022 |
| 5570 | Machaon Diagnostics Berkeley, CA Clinical Laboratory Assistant B.A./B.S with coursework in chemistry, biochemistry, immunology, molecular biology, statistics and related subjects required. Exp: 6 months or more |
Demonstrate proficiency and understanding of standard clinical laboratory practices. Review requisitions, orders tests and processes specimens in preparation for laboratory procedures. Perform general laboratory maintenance tasks including preparing reagents, re-stocking consumables and washing glassware. Assist with quality control and quality assurance paperwork. Assist with clinical trials including completion of Institutional Review Board documentation, subject recruitment, screening, and management, and performance of research related testing. Design and revise forms and protocols. Adhere to Machaon policies and procedures as directed by the supervisor, manager or medical director. Interact with patients, subjects, visitors, physicians, and coworkers in a professional and courteous manner. | 12/13/2022 |
| 5571 | Marker Therapeutics Houston, TX Cell Therapy Manufacturing Technician BS, MS in Biology or a related science Exp: 1-5+ years |
Marker Therapeutics is seeking a cell therapy technician for its manufacturing group to support its ongoing efforts to develop immunotherapies for the benefit of patients with cancer. This position will work under the guidance of the Senior Director of CMC and perform assigned responsibilities to support the company’s product manufacturing process and process improvement initiatives. | 12/14/2022 |
| 5572 | Matica Biotechnology College Station, TX Manufacturing Associate AS/BS in Biotechnology, Biology, Chemistry, or equivalent. Exp: 0-2 years |
The successful candidate for manufacturing associate will execute the daily manufacturing schedule communicated by the Manufacturing Supervisor to include but not limited to cell expansion, bioreactor operations and purification techniques (TFF and Chromatography) for viral vector manufacturing processes. | 12/14/2022 |
| 5573 | Medtronic Bedford, MA Quality Engineer II Master's Degree in Engineering or Technically Related discipline. Exp: 0 years |
Medtronic Cardiac Ablation Solutions Group (CAS) is searching for a Quality Engineer II to join our growing Quality Operations team in Bedford, MA. In this role, you will be responsible for various programs within our Quality Management System and for driving day-to-day compliance in the development and manufacturing of leading-edge medical devices. We are looking for bright, hands-on individuals who are interested in making a difference in a dynamic and exciting entrepreneurial environment. The ideal candidate will be a motivated individual looking to grow professionally in a fast-paced environment. Strong analytical skills, excellent knowledge of theoretical and practical fundamentals, and a solid ability to work on multiple projects simultaneously are required. | 12/15/2022 |
| 5574 | Medtronic Santa Ana, CA Microbiologist II Master's Degree in Microbiology or Related discipline Exp: 0 years |
In this exciting role as a Microbiologist-Sterilization II you will have responsibility for supporting on market product sterilization validations. You will have responsibility for sustaining sterilization work and to support of changes to existing products and introduction of new products. These validations include product sterilization validations, along with product and process validations. The position provides technical solution to achieve validated sterilization processes for new and existing products. Updates to routine sterilization procedures and related specifications. Supports and leads team with assessments of new products or changes to existing products. | 12/15/2022 |
| 5575 | Medtronic Irvine, CA Microbiologist-Sterilization II - Irvine, CA Advanced degree in science or technical field Exp: 0+ years |
In this exciting role as a Microbiologist-Sterilization II you will have responsibility for supporting on market product sterilization validations. You will have responsibility for sustaining sterilization work and to support of changes to existing products and introduction of new products. These validations include product sterilization validations, along with product and process validations. The position provides technical solution to achieve validated sterilization processes for new and existing products. Updates to routine sterilization procedures and related specifications. Supports and leads team with assessments of new products or changes to existing products. | 12/15/2022 |
| 5576 | Medtronic North Haven, CT Chemist II Master's Degree in Chemistry, Biology, Material Science, or related technical discipline Exp: 0 years |
The chemist will be primarily responsible for performing Extractable and Leachable Extractions and Inductively Coupled Plasma- Mass Spectrometry (ICP-MS) data analysis and testing support in an analytical chemistry lab. The position has responsibility for project-based sample preparation, operation of ICP-MS instrumentation, data processing, and quantitation for chemical characterization in accordance to ISO10993. The role functions as part of an analytical chemistry team that works under ISO 13485 and ISO 17025 Quality Management Systems. | 12/15/2022 |
| 5577 | Medtronic Santa Rosa, CA R&D Engineer II - Transcatheter Heart Valve Therapies Advanced degree in Engineering. Exp: 0+ years |
This is an exciting opportunity to join Medtronic's Structural Heart business unit to work with a dedicated team focused on the development and expansion of our new transcatheter heart valve replacement system. In this role, the Engineer II will be working on the delivery system team to develop, qualify, and commercialize the device. | 12/15/2022 |
| 5578 | Medtronic Boston, MA Systems Engineer II - Surgical Robotic Master's Degree in Engineering or Technically Related discipline. Exp: 0 years |
This position is in the Boston, MA office, reporting to the Integration Site Lead in the Systems Integration Center of Excellence. The System Engineer II is a technical individual contributor role within the R&D engineering team that is developing Medtronic’s Robotic Assisted Surgical Device (RAS). This candidate shall have an engineering mindset and contribute to logistics that support enabling development teams to utilize the capital equipment on a variety of project variants. This role will include aspects of fleet repairs, inventory management, planning, tracking, allocation of hardware and documentation related to the robotic system and its components. | 12/15/2022 |
| 5579 | Merieux NutriSciences Salt Lake City, UT Microbiologist Bachelors preferred Exp: One (1)- 2 years |
We are looking for a Microbiologist in 1945 Fremont Drive, Salt Lake City, UT 84104 USA. Your mission will be to: Follow appropriate methods and SOPS on all tasks. Maintain quality control records Read, calculate, record data in Laboratory Information Management System Perform rapid test methods Perform confirmation tests on suspect samples to identify the strain of bacteria Read, enter and evaluate process control samples Maintain knowledge of Laboratory Information Management System (LIMS) that is required to complete job responsibilities Support root cause analysis investigations and suggest appropriate corrective actions Weigh appropriate amount of sample and pour correct agar to begin analysis procedures. Write identification onto plates so that client and sample number can be tracked | 12/15/2022 |
| 5580 | Merieux NutriSciences Cypress, CA Microbiology Technician Bachelor’s degree required. Exp: no experience |
No previous laboratory experience is required - we will provide full training. ▪Read plates and tubes, as required, to determine the number of organisms in the sample ▪Record findings on worksheet for verification ▪Write identification onto plates so that client and sample number can be tracked ▪Pipette sample solution into tubes or plates according to the analysis process being performed ▪Pour the agar into plates or tubes to begin the growth process ▪Prepare sample for analysis by recording, weighing, and blending ▪Collect plates and place them in the incubator for the specified amount of time and temperature ▪Prepare media and broth for use in pathogen testing as required ▪Sterilize materials needed for analysis. Autoclave plates before discarding ▪Perform food poisoning, pH and other analysis tests on sample when requested by the client ▪Ensure that media and materials are prepared for the next testing sequence ▪Maintain knowledge of Laboratory Information Management System (LIMS) that is required to complete job responsibilities ▪Set up equipment and materials needed for analysis | 12/16/2022 |
| 5581 | Merieux NutriSciences Crete, IL Microbiologist Bachelors preferred. Exp: One (1)- 2 years |
▪Follow appropriate methods and SOPS on all tasks.Maintain quality control records ▪Read, calculate, record data inLaboratory Information Management System ▪Perform rapid test methods ▪Perform confirmation tests on suspect samples to identify the strain of bacteria ▪Read, enter and evaluate process control samples ▪Maintain knowledge of Laboratory Information Management System (LIMS) that is required to complete job responsibilities ▪Support root cause analysis investigations and suggest appropriate corrective actions ▪Weigh appropriate amount of sample and pour correct agar to begin analysis procedures.Write identification onto plates so that client and sample number can be tracked▪Follow appropriate methods and SOPS on all tasks.Maintain quality control records ▪Read, calculate, record data inLaboratory Information Management System ▪Perform rapid test methods ▪Perform confirmation tests on suspect samples to identify the strain of bacteria ▪Read, enter and evaluate process control samples ▪Maintain knowledge of Laboratory Information Management System (LIMS) that is required to complete job responsibilities ▪Support root cause analysis investigations and suggest appropriate corrective actions ▪Weigh appropriate amount of sample and pour correct agar to begin analysis procedures.Write identification onto plates so that client and sample number can be tracked | 12/16/2022 |
| 5582 | Merieux NutriSciences Crete, IL Chemist I Bachelors preferred. Exp: One - two years |
Analyses w/Extractions (Cholesterol, FAP, ICP, MOJO, FFA, etc.) Ensure that proper analysis methods are conducted on the appropriate samples. Maintain chemistry quality control records and procedures for each test. Extract desired components from samples with appropriate processes such as distillation, solvent extraction and acid digestion, so that concentrations can be determined. Calculate the concentration of components present in samples and post results. Wash glassware as needed and prepare samples as needed. Prepare standards or reagents that are needed for the analysis procedure. Maintain knowledge of Laboratory Information Management System (LIMS) required to complete job responsibilities. Maintain clean laboratory by washing countertops, sweeping floors, storing analysis materials, etc. | 12/16/2022 |
| 5583 | Merieux NutriSciences Crete, IL Chemist III Masters degree. Exp: 1-2 years |
Purpose (Objective): The incumbent is responsible for performing chemical analysis on food, pharmaceutical, and other sample. The incumbent analyzes the concentration of certain components in food samples. The incumbent must accurately prepare and process the sample to obtain the required results. The incumbent observes daily activities of departmental personnel ranging from receiving to reporting of results and ensures that analysis is performed correctly. | 12/16/2022 |
| 5584 | Meso Scale Discovery Rockville, MD Chemist BS in Chemistry, Biochemistry or related field. Exp: 1 year |
Chemist needed to: perform organic syntheses to manufacture compounds for use in company products; monitor reactions in-process using HPLC and TLC to determine progress; purify reactions using size-exclusion chromatography and recrystallization to measure process yields; analyze purified products by HPLC and TLC to determine levels of purity; interpret NMR and MS spectra to determine identity of synthesized compounds; operate lyophilizers and automated crimping and labeling equipment to produce lyophilized vials. | 12/16/2022 |
| 5585 | Meso Scale Discovery Gaithersburg, MD Research Associate Bachelor’s degree in life sciences, or related area is required. Master’s degree a plus. Exp: 1 - 3 years |
This position is responsible for executing experiments and analyzing the resulting data in support of reagent and assay development projects with close supervision. This is a laboratory-based position responsible for advancing research and/or development objectives focused on leading-edge biomarker measurements and technology. | 12/16/2022 |
| 5586 | Meso Scale Discovery Gaithersburg, MD Research Associate, Recombinant Antibodies Bachelor’s degree in life sciences, or related area is required. Master’s degree a plus. Exp: 1 - 3 years |
This position is responsible for executing experiments and analyzing the resulting data in support of reagent and assay development projects with close supervision. This is a laboratory position to apply various molecular biological tools and techniques to develop new recombinant antibodies and other proteins. | 12/16/2022 |
| 5587 | Meso Scale Discovery Gaithersburg, MD Research Associate Bachelor’s degree in life sciences, or related area is required. Master’s degree a plus. Exp: 1 - 3 years |
This position is responsible for executing experiments and analyzing the resulting data in support of reagent and assay development projects with close supervision. This is a laboratory-based position responsible for advancing research and/or development objectives focused on leading-edge biomarker measurements and technology. | 12/16/2022 |
| 5588 | Meso Scale Discovery Gaithersburg, MD Research Associate Bachelor’s degree in life sciences, or related area is required. Master’s degree a plus. Exp: 1 - 3 years |
This position is responsible for executing experiments and analyzing the resulting data in support of reagent and assay development projects with close supervision. This is a laboratory-based position responsible for advancing research and/or development objectives focused on leading-edge biomarker measurements and technology. | 12/16/2022 |
| 5589 | Meso Scale Discovery Gaithersburg, MD Cell Culture Specialist I Cell Culture Specialist I Bachelor's degree in Biology, Chemistry, Biotechnology, Engineering or a related field . Exp: six months |
This position is responsible for the production of cell-based products including but not limited to hybridoma antibodies and recombinant antibodies. | 12/16/2022 |
| 5590 | Mevion Medical Systems Littleton, MA Electrical Manufacturing Engineer, Entry/Mid level Bachelor of Science degree in Electrical Engineering, Robotics Engineering, or equivalent. An advanced degree is desirable. Exp: 1+ years |
The Electrical Manufacturing Engineer will Provide manufacturing engineering support in the design, manufacture, installation, and acceptance testing of a medical proton particle accelerator and its support systems. | 12/16/2022 |
| 5591 | Microbiologics Saint Cloud, MN Senior Research and Development Associate, Saint Cloud Master’s degree in related field Exp: 0-2 years |
Microbiologics, a leader in providing external controls for molecular diagnostic assays is seeking to expand its Product Development Team with the addition of an experienced Senior R&D Associate trained in molecular biology and assay diagnostics. The Senior Associate will design, lead, perform and report on experiments using microbiology and molecular techniques leading to new products or process improvements in an FDA-QSR and ISO13485 compliant organization. The ideal candidate will have experience in product commercialization, expert knowledge of concepts (such as nucleic acid extraction, real time PCR and Digital PCR), and a high level of scientific creativity and technical proficiency. | 12/16/2022 |
| 5592 | Miromatrix Medical Eden Prairie, MN Per Diem Technician - Part Time Cell Isolation Team Associates degree or working on BS in one of the Life Sciences disciplines including Biology, Cell Biology, or Microbiology Exp: 0+ - 2 years |
Assists with tissue/sample production according to established plans and maintains records in compliance with Miromatrix policy and GMP. Assists in testing and quality control of cell or tissue samples. Works directly with supervisor, team lead, and other team members during production and independently for most testing and quality control once fully trained. | 12/16/2022 |
| 5593 | Moderna Therapeutics Cambridge, MA Research Associate, Infectious Disease Research Master’s degree in Biochemistry, Cell biology or related discipline. Exp: 0-1 years |
Moderna is seeking a talented and experienced Research Associate to work on protein production, purification and characterization to help discover and develop new mRNA vaccine antigens to prevent and treat infectious diseases (ID). The candidate will work with collaboratively internal teams to help advance the infectious disease mRNA vaccine portfolio. Research will involve antigen discovery, characterization and evaluation for in vitro and in vivo analyses, including production of antigens for clinical biomarker readout. The candidate will work in a matrixed working environment, interact and facilitate collaborations with internal and external research partners. Applicants should be outstanding at lab-based research, a collaborative team member and an excellent communicator. | 12/16/2022 |
| 5594 | Moderna Therapeutics Norwood, MA Research Associate in LNP Process Science BS or MS in Bio/Chemical Engineering, Chemistry, or closely related field Exp: 0-2 years |
Moderna is seeking a highly skilled and motivated process development scientist to develop lipid nanoparticles (LNPs) within the Technical Development organization. This role will develop, scale-up, and transfer new and improved production processes for Moderna’s first-in-class messenger RNA (mRNA) based medicines to enable our clinical supply and late-stage development. | 12/16/2022 |
| 5595 | Moderna Therapeutics Norwood, MA Research Associate, Process Development Bachelors in biochemistry, chemistry, molecular biology, chemical engineering, biological engineering or a related discipline. Exp: 0‑2 years |
Moderna is working to develop first-in-class messenger RNA (mRNA) based medicines. We’re seeking a highly skilled and motivated Research Associate to reside in Moderna’s Technical Development organization in Norwood, MA. This is a lab-based role that will support the early phase process development of Moderna’s mRNA-based medicines to enable our clinical supply and pipeline. The applicant should have strong communication and collaboration skills. | 12/16/2022 |
| 5596 | Moderna Therapeutics Norwood, MA Engineer I, Process Development BS/MS in Chemical Engineering, Chemistry, Biochemical Engineering, Biochemistry or closely related field. Exp: 0-3 years |
Moderna is working to develop first-in-class messenger RNA (mRNA) based medicines. We are seeking a Bioprocess scientist or engineer to reside in Moderna’s Technical Development organization in Norwood, MA. Our team’s goal is to envision, pilot, scale, characterize, transfer, and validate robust commercial GMP manufacturing processes. We seek applicants who are proactive, enthusiastic, and show a passion for process development. | 12/16/2022 |
| 5597 | Moderna Therapeutics Norwood, MA Associate Specialist, Manufacturing Bachelor's Degree in Engineering or Life Sciences is preferred. Exp: 1-3 years |
This Associate Specialist will be part of a cohesive team responsible for producing high quality mRNA-based medicines for commercial production and evaluation in human clinical trials. The Associate Specialist uses expert knowledge of cGMP regulations and biopharmaceutical production processes to support day to day operational support through deviation and CAPA writing with a focus on but not limited to Commercial Lipid Nanoparticle Manufacturing. | 12/16/2022 |
| 5598 | Moderna Therapeutics Norwood, MA Associate Specialist, Manufacturing (Batch Specialist) Bachelor's Degree in Engineering or Life Sciences is preferred. Exp: 1-3 years |
The individual in this role will be part of a cohesive team responsible for producing messenger RNA for commercial production or for evaluation in human clinical trials. This position will specifically focus on batch readiness and batch close out activities. The Manufacturing Associate Specialist uses knowledge of manufacturing biopharmaceutical unit operations, quality systems and digital infrastructure to as act as a batch readiness and close out lead for the team. The Specialist will be a key team member maintaining the production schedule, managing batch record close out and Manufacturing owned actions supporting product disposition. They will leverage knowledge of cGMP regulations to support some investigations and improvement initiatives within manufacturing operations. Additional functions include acting as a responsible liaison between the Manufacturing group and other partner groups (Facilities, Supply Chain, QA, etc.) This role will also work cross-functionally to assist in planning manufacturing activities, maintenance and calibration of equipment and instruments and provide oversight of batch close out work such as batch record review and completion. The Specialist must be technically capable with a good theoretical comprehension of general biopharmaceutical manufacturing equipment, principles and processes. The successful candidate must have a good understanding of current GMP and safety standards and be able to apply this knowledge in a GMP environment. | 12/16/2022 |
| 5599 | Genomatica San Diego, CA Research Scientist I Bachelor’s, Masters, or Doctorate in Chemistry, Biochemistry, Biology or related fields Exp: 0-2 years |
Genomatica is seeking a scientist with experience in analytical chemistry or a related field to work as a member of the Analytical Sciences team. The team is responsible for quantitative analysis of fermentation, and DSP impurity/purity profiles using HPLC, GC and IC analytical systems. Furthermore, the scientist would be responsible for identifying unknowns in these materials and for developing quantitative and qualitative methods for analysis thereof. The results generated will provide valuable data and insights for our internal project development and bioprocess development and optimization as well. You will perform lab duties under the supervision and mentorship of senior analytical personnel. You will contribute to multiple projects daily and ultimately to the long-term success of the company. You will utilize a variety of analytical chemistry techniques to support and help advance Genomatica strain engineering and process technology platforms. | 12/6/2022 |
| 5600 | GenScript Piscataway, NJ Research Scientist – Automated Process Development Ph.D., MS Biology/ Biochemistry/ Molecular Biology/ Biomedical Instrumentation/ Bioengineering Discipline or related subjects Exp: 1 year (for MS candidates) |
We are looking for a Research Scientist – Automated Process Development to support the key high throughput molecular biology reagent production needs in the US Molecular Biology/ Reagent services business unit. | 12/6/2022 |
| 5601 | Glaukos San Clemente, CA MANUFACTURING TECH I/II, 2ND SHIFT Bachelor's degree in science or engineering Exp: 0-2 years' |
Prepare components and build assemblies Prepare bulk drug formulations | 12/7/2022 |
| 5602 | Glaukos San Clemente, CA ENGINEER I/II Master’s degree in Mechanical, Biomedical, Chemical Engineering or equivalent; Bachelors’ degree in Mechanical, Biomedical, Chemical Engineering or e Exp: MS: 0-2+; BS: 1-3 years |
Developing manufacturing processes, production scale-up, and sustaining support Developing creative solutions to manufacturing problems Development and execution of process, equipment, and product validations/qualifications Ensuring engineering deliverables are accurately generated, via 3D CAD models and 2D CAD drawings for assembly tools, fixtures, and clinical supplies Leading manufacturing related project teams (i.e. engineers, technicians, and manufacturing staff) with a focus on meeting manufacturing requirements while taking a high quality/cost effective approach. | 12/7/2022 |
| 5603 | Global Pharma Tek San Diego, CA Scientist 1, Analytical Chemistry Development B.S. Degree in Chemistry, Engineering, or Life Science Exp: 1 to 3 years |
The Quality Control Chemist I conducts various analytical testing of raw materials, semi-finished intermediates, finished products, and new compounds/products in various stages of design and development to characterize and determine quality. | 12/7/2022 |
| 5604 | Global Pharma Tek Charles City, IA Scientist BA/BS in Science related Field Exp: 0 - 1 year |
Daily testing of samples received from production. Timely completion of tests to meet the established testing time. Following GMP documentation guidelines. The colleague should have ability to follow detailed instructions and have basic problem solving skills and ability to trouble shoot issues that may arise when testing. Colleague must be willing to contribute to the teams productivity and overall goals. | 12/7/2022 |
| 5605 | Grand River Aseptic Manufacturing Grand Rapids, MI QC Microbiology Technician (2nd and 3rd Shift) Bachelor’s degree in microbiology or a related field Exp: 0-2 years’ |
The Microbiology Technician supports quality control and assurance by assisting the microbiology department with environmental monitoring, water testing, and client specific testing. | 12/7/2022 |
| 5606 | Grifols Research Triangle Park, NC Assoc. Research Scientist II/Sr. Assoc. Research Scientist I Senior Associate Research Scientist I: Degree must be within a relevant field: (Biology, Biochemistry, Chemistry, or Toxicology) Masters; Associate Re Exp: SARSI: + 1 year ; ARSII: MS 0 years; BS 1-2 years. |
The selected candidate provides analytical testing support for process characterization, developmental stability studies, and release of preclinical or clinical batches for internal research projects. The individual selected for this position will conduct testing of non-routine sample types in support of process development, characterization, and/or validation and compile data for the generation of multi-user interactive analytical databases. The analyst may participate in development, implementation and validation of new analytical techniques. | 12/7/2022 |
| 5607 | GRO Biosciences Cambridge, MA Research Associate/Sr RA, Chemistry Expansion MS degree or BS/BA degree in biology, microbiology, biotechnology, biological engineering, or related field Exp: MS: 0 year; BS: 1 year |
The selected candidate for this position will work within the Chemistry Expansion division, enabling the scalable incorporation of new amino acids into proteins. Major job responsibilities include development and screening of translation machinery for new amino acids, and general engineering of ribosomal translation. Day-to-day activities include design and execution of experiments in conjunction with other team members. Diligence, transparent communication, and record keeping will be critical skills to enable success in this position. Your creativity and ingenuity will be crucial to driving GRObio’s research priorities optimizing strain performance and expanding the amino acid alphabet to create differentiated products. | 12/7/2022 |
| 5608 | GlaxoSmithKline King of Prussia, PA Associate Scientist- Bio Pharm Drug Substance Process Development Master's degree (Chemical Engineering, Biochemistry, Chemistry or Biology) Exp: 0 - 1 year |
As an Associate Scientist in Downstream Process Development, you will be a member of a highly skilled team of scientists and engineers responsible for the evaluation and optimization of purification processes. You will be involved in all aspects of the development of purification processes including initial process screening, optimization and characterization, scale-up and tech transfer to clinical manufacturing and/or commercial manufacturing partners for therapeutic proteins including monoclonal antibodies, and antibody-drug conjugates. Your primary focus will be on the bench-scale laboratory development of purification unit operations such as column chromatography (affinity, ion exchange, HIC, mixed mode, etc.), ultrafiltration, depth filtration and continuous centrifugation. Although predominantly lab-based, the role also involves verbal and written communication and requires good organization. Both individual and team working are required and therefore the role will suit a scientist with good interpersonal skills, self-motivation and an open mindset. | 12/7/2022 |
| 5609 | GlaxoSmithKline Rockville, MD Associate Scientist Bachelor's degree (biotechnology, molecular biology, biochemistry, molecular, bacteriology, molecular, microbiology). Exp: One or more years |
As Associate Scientist within the Molecular Analytics platform, you will be in charge of implementing, designing and developing methods for the detection and quantification of nucleic acids based on up-todate nucleic acid technologies (NAT) and, in particular, methods aiming at characterizing plasmids (topology, conformation, sequence, quantity, etc.), mRNA Drug Substances (content, integrity, identity) and mRNA-LNP Drug products (monovalent and multivalent), used for production of mRNA vaccines. The use of direct nucleic acid quantification methods (e.g. CRISPR-based assays, digital counting through optical barcodes, branched DNA assays, etc.) will part of the activities of the hired Scientist. | 12/7/2022 |
| 5610 | GlaxoSmithKline Hamilton, MT QC Systems Support Specialist Bachelor's Degree in a scientific discipline Exp: 1+ years |
As a QC Systems Support Specialist, you will manage non-testing laboratory support systems and processes for QC, including: Maintaining SAP Modules, Master Data/Monograph Creation, Compendial Review, Equipment Qualification/Lifecycle, and Method Validation/Transfer. In this role, you will serve as a Lead Investigator for select QC Unplanned Events, as well as change coordinator for selected QC Change Controls. In addition, you will author QC Technical Documents, such as validation and trend reports and provide data for annual PQR. | 12/7/2022 |
| 5611 | GlaxoSmithKline Rockville, MD Associate Scientist, Physical & Chemical Analytics Bachelors/Masters in Sciences/Engineering discipline Exp: BS: 1-4 years ; MS: 0-2years |
In this role you will be the Strategic Insight Business Partner to the Global RSV Adult Vaccine Commercialization Leader (VCL). This role will provide YOU the opportunity to deliver key activities to progress YOUR career.In this role you will be the Strategic Insight Business Partner to the Global RSV Adult Vaccine Commercialization Leader (VCL). | 12/7/2022 |
| 5612 | HelixBind Boxborough, MA Formulation Technologist Certificate, Associate’s or Bachelor’s degree in a science or engineering discipline Exp: 0-5 years’ |
We are seeking a talented and motivated individual to join our R&D Team as a Formulation Technologist. This is a great time to join our team. The position offers the exciting opportunity to grow along with the Company as we take our initial product through FDA clearance and market launch while, in parallel, build out our pipeline of impactful syndromic diagnostic assays. | 12/8/2022 |
| 5613 | Heron Therapeutics San Diego, CA Senior Research Associate I-III M.S. in chemistry or related subject. Exp: 1+ years |
The qualified candidate will join the Pharmaceutical Sciences team to develop, qualify, and implement characterization and quantitative analysis of Heron products, including polymers, oligomers, and small molecules. Desirable skills include mass spectrometry, HPLC, GC, and other physico-chemical methods. | 12/8/2022 |
| 5614 | Hexagon Bio Menlo Park, CA Research Associate/Senior Research Associate, Chemical Biology BSc or MSc in chemistry, biochemistry, chemical biology, microbiology, molecular biology, or a related discipline Exp: 1+ years |
We are searching for a high-caliber Research Associate who has experience with modern molecular biology, genetic engineering, and chemical analysis. The ideal candidate is excited to solve scientific questions, interested in discovering new therapeutics, and energized by working with a dynamic, data-driven team. We would like team members to be thoughtful, meticulous, well-organized, team-oriented, and fully engaged in the execution of the workflow. | 12/8/2022 |
| 5615 | Hexagon Bio Menlo Park, CA Research Associate/Senior Research Associate, Fungal Microbiologist B.S. or M.S. in microbiology, plant pathology, microbial ecology or other related field Exp: 1+ years |
We are searching for a highly motivated Research Associate on the Sequence the Earth team. You’ll play a critical role in Hexagon Bio’s efforts to unlock the biosynthetic potential of the kingdom Fungi. Your primary contributions will include: culturing, documenting, and maintaining a diverse collection of fungi. You’ll contribute to both manual, and robotics-aided high-throughput culturing and genomic DNA/RNA extraction workflows, manage strain-frozen stocks and activation and enhance the efficiency and quality of these processes. You’ll work closely with our Fungal Genetics team, Automation Engineers, and Software Engineers to develop methods vital to these tasks. Applicants with a strong handle on microbiology and the diversity of phenotypes and growth habits of filamentous fungi are encouraged to apply. This is an ideal position for someone with experience in an academic or industrial microbiology laboratory setting culturing diverse fungi from existing collections and/or nucleic acid extractions from filamentous fungi. | 12/8/2022 |
| 5616 | ICU Medical Austin, TX Analyst I, Chemistry - (22301793) Bachelor’s Degree is required: Chemistry, Chemical Engineering, or Chemical Science Exp: 0-2 year |
The Chemistry Analyst I will work under direct supervision or be partnered with an experienced analyst to perform wet chemistry analyses, preparation of reagents, standardization of solutions, and instrumentation testing and documentation in a cGMP environment. May be cross-trained to work in other laboratory areas as dictated by the needs of the department. | 12/8/2022 |
| 5617 | Invitae San Francisco, CA DNA Extraction Technician Bachelor’s degree in clinical laboratory studies or equivalent science related studies Exp: 1+ years |
Thur-Mon, 3:00pm-11:30pm We're looking for passionate laboratory technicians who will support high complexity laboratory testing on patient specimens across various assays and platforms. This role will be performing quality control and quality assurance procedures while complying with all applicable local, state and federal laboratory requirements. The work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask and be flexible with tasks and schedules, and the ability to work independently in a team environment. This role requires on-site work at our San Francisco location as well as ability to work overtime and off-schedule days as needed. | 12/8/2022 |
| 5618 | Invitae San Francisco, CA Lab Technician Bachelor's degree in clinical laboratory studies or equivalent science related studies, Exp: 1+ years |
Sunday - Thursday, 3:00pm - 11:30pm We're looking for passionate laboratory technicians who will support high complexity laboratory testing on patient specimens across various assays and platforms. This role will be performing quality control and quality assurance procedures while aligning with all applicable local, state and federal laboratory requirements. The work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask and be flexible with tasks and schedules, and the ability to work independently in a team environment. The team's culture is one in which direct and consistent feedback can be given and taken; we encourage honest and open communication and constructive feedback. We rely on team members to work with a sense of urgency and with a goal of putting the team above the individual. We prioritize transparency and continuous process improvement to contribute towards the highest level of patient care. | 12/9/2022 |
| 5619 | Ionis Pharmaceuticals Carlsbad, CA Research Associate / Senior Research Associate, Neurology Research M.S Exp: >1-3 years |
onis Pharmaceuticals is seeking a highly qualified individual to join our Neurology research group. Our Neurology research group is currently applying Ionis’ antisense oligonucleotide (ASO) technology to develop treatments for various neurodegenerative diseases. The ideal candidate is self-motivated, excellent communicator, strongly committed to the scientific process, and capable of working independently as well as collaboratively in a fast-paced environment with strict deadlines. Key responsibilities include execution of in vivo and in vitro studies, performing assays, analyzing and presentation of data to support drug discovery efforts. This is an individual contributor position with most of the work being performed in a laboratory setting. | 12/9/2022 |
| 5620 | Ivenix Grand Island, NY ASSOCIATE SCIENTIST - 1st Shift (Chemistry) B.S. in Chemistry, Biology, or related physical science. Exp: 0-2 years |
An Associate Scientist is responsible for performing entry level chemical testing to support raw material, in-process, stability, and finished products as required for Quality Control. Effectively communicates work and results both orally and in writing. | 12/9/2022 |
| 5621 | Ivenix Grand Island, NY ASSOCIATE SCIENTIST - 1st Shift B.S. in Chemistry, Biology, or related physical science. Exp: 0-2 years |
An Associate Scientist is responsible for performing entry level chemical testing to support raw material, in-process, stability, and finished products as required for Quality Control. Effectively communicates work and results both orally and in writing. | 12/9/2022 |
| 5622 | JOINN Biologics Richmond, CA Analyst I, II or Sr Analyst - QC Analytical MS Exp: 0-2 years |
We are searching for a highly motivated Quality Control Analyst who preferably has a minimum of 2 years of experience working in cGMP quality control laboratory environment with expertise in wet and protein chemistry to join our team. The candidate will be responsible for the qualification and execution of analytical laboratory tests and evaluations of product performance and processes in the Quality Control Department, in accordance with approved methodologies, policies, and associated regulations. | 12/9/2022 |
| 5623 | JOINN Biologics Richmond, CA Associate I - QA Bachelor’s degree in a scientific and/or technical discipline related to biology, biotechnology, chemistry or pharmaceutics. Exp: • 1+ years |
The QA Associate will be responsible for the overall strategy and oversight of JOINN Biologics Quality and Compliance for API and final product. This candidate will be writing protocols and must have strong communication, technical writing, and statistical analysis skills. | 12/9/2022 |
| 5624 | KBI Biopharma Louisville, CO Research Associate I/II B.S. Exp: 0-2 years |
Open position available in the biophysical characterization core of the rapid analytics testing group. Responsible for analytical testing of client samples. Testing may include using client-based methods or some method development. Ideal candidate is able to quickly and accurately generate results. Technical writing skills are a plus. | 12/9/2022 |
| 5625 | KBI Biopharma Durham, NC Manufacturing Specialist - Downstream Master’s degree in a related scientific or engineering discipline preferred Exp: 0+ year’s |
The manufacturing specialists on the operations team will support the startup and ongoing manufacturing operations at a new biopharmaceutical manufacturing facility. The individual will report to the associate director of manufacturing in support of upstream, downstream, or manufacturing support. The individual will be responsible for supporting equipment and operations for the upstream, downstream, and/or manufacturing support teams. The ideal candidate will have experience supporting the startup and ongoing operations for a commercial GMP mammalian cell culture facility. Expertise using single-use bioprocessing equipment and materials is highly desired. Experience with cell culture, chromatography, filtration, and/or solution preparation operations is required for Specialist I and higher levels. | 12/9/2022 |
| 5626 | KBI Biopharma Boulder, CO Research Associate I/II Bachelor of Science Degree in Biochemistry, Molecular Biology, Biopharmaceutical Development or related disciplines Exp: 1-3 years |
Perform contract testing services, including in-process and GMP release testing, GMP stability testing, method transfer activities, and qualification/validation activities for monoclonal antibodies, recombinant proteins, and peptides. | 12/9/2022 |
| 5627 | KBI Biopharma Durham, NC Microbiology Associate I/II Bachelor’s/Master’s degree in Microbiology, Biology or related technological field of science. Exp: BS: 1-2 years; MS: 0-1 years |
Sunday, Monday, Tuesday, Wednesday (Sun-Wed) Position. Second shift 1pm-11:30pm. This position is eligible for a shift differential. The Microbiology Associate will be part of the Microbiology Department responsible for the testing and support for the Microbiology Laboratory in support of a Contract Manufacturing biotechnology facility and Process Development. Responsibilities includes laboratory support, program testing, reporting of results, execution of protocols. | 12/9/2022 |
| 5628 | KBI Biopharma Durham, NC Manufacturing Associate I/II-Upstream (Nights) Manufacturing Associate I: Bachelor’s degree in a related scientific or engineering discipline. Exp: 0-2 years’ |
This position is on a 2-2-3 schedule, with the hours 7p-7a. The Manufacturing Associate I/II – Upstream is responsible for the execution of production activities for early and late-phase Cell Culture programs within a GMP environment. The Manufacturing Associate I/II – Upstream must follow the instructions depicted in SR’s, EPR’s, BR’s, SOP’s and forms. Additionally, must ensure all work is conducted following Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and Good Laboratory Practices (GLP); including ‘Right the First Time’ (RFT). Upstream is responsible for the execution of production activities for early and late-phase Cell Culture programs within a GMP environment. | 12/9/2022 |
| 5629 | KBI Biopharma Durham, NC In Process Research Associate BS in scientific discipline or equivalent Exp: 0-2 years’ |
KBI Biopharma, Inc. is a contract services organization committed to reducing process development time, decreasing production cost and increasing speed of development for biopharmaceuticals. We are seeking an In-Process Support Associate with strong protein chemistry background to perform cGMP in-process analytical support. These services include in-process and release testing for drug substances manufactured internally. | 12/9/2022 |
| 5630 | Key Tech Baltimore, MD Electrical Engineer (Full-Time & Intern Positions) BS or MS Electrical Engineering degree from leading university/college Exp: Up to five years |
We’re actively hiring for full-time engineers as well as spring, summer and fall interns (electrical, computer, and mechanical) with competitive well paid salaries and benefits. Our interns work on real engineering challenges from day one. Everyone who starts at Key Tech jumps right into interesting, creative high tech work. With a blend of challenging work, smart coworkers, and the best company culture, Key Tech is the right company for you. | 12/9/2022 |
| 5631 | Key Tech Baltimore, MD Computer Engineer - Firmware/Software (Full-Time & Intern Positions) Computer Engineering or Computer Science degree Exp: up to 5 years |
Key Tech is hiring computer engineers who crave doing fun and challenging custom embedded systems design. As a computer engineer at Key Tech, you'll create firmware and software that interacts with the real world. Develop embedded algorithms that drive motors, move mechanisms, measure optical signals and communicate with PC software. Help pick processors and design embedded architectures that will be in the next generation of medical devices. Test your code on custom Key Tech designed boards - see your software in action. Interested in designing a complex code base to control microfluidic flow? Want to be challenged with designing a thermal control system which simultaneously measures optical signals? Intrigued by creating code that controls a pneumatic system for DNA analysis? | 12/9/2022 |
| 5632 | Khloris Biosciences Mountain View, CA Cell Therapy Manufacturing Technician B.S. degree in biology, biochemistry, bioengineering, or related technical field, or equivalent industry experience. Exp: 0-5 years |
Khloris Biosciences, Inc. is seeking innovative and highly motivated cell therapy manufacturing technician to join our team. The selected candidate will work closely with lead manufacturing technicians, scientists, participate in project and team meeting, and work in a multidisciplinary environment. The duties of this position will involve supporting a multidisciplinary manufacturing team in developing Khloris cell therapy platforms. The ideal candidate will have hands-on expertise and comprehensive understanding of cell therapy manufacturing processes | 12/9/2022 |
| 5633 | Lannett Seymour, IN Product Chemist I BS Degree in Chemistry or related field Exp: 0+ years |
This position is primarily responsible for the laboratory testing of in-process, release and stability samples for commercial drug products. | 12/9/2022 |
| 5634 | Lantheus Medical Imaging Billerica, MA Research Scientist I BS/BA/MS in Chemistry, Pharmaceutics, Engineering or equivalent. Exp: MS: 1-2 years |
Radiochemist/Chemist to conduct radiolabeling studies to support R&D portfolio of new and existing products. Requirements include technical expertise in optimization and troubleshooting of synthesis processes, interaction with and transfer of radiolabeling methodology to contract manufacturing sites, and competency in use of HPLC, UV, radio-detection, LCMS and iTLC methodology. Handling of positron and gamma radionuclides for small scale radiolabeling experiments and analytical analysis of both research and commercial products is required. Communication with contract research organizations required for external studies using R&D test compounds. Data interpretation, issue resolution as needed and final report writing is also required. | 12/9/2022 |
| 5635 | Loop Genomics San Diego, CA Research Associate, System Integration BS degree in chemistry, physics, molecular biology, bioengineering or similar field Exp: 1+ years |
The ideal candidate is a generalist at-heart and be comfortable learning and working in diverse disciplines including hardware, software, molecular biology and biochemistry. Your efforts will significantly contribute to a suite of products and improvements that will help shape the future of biology and change how we evaluate and measure both health and disease. | 12/9/2022 |
| 5636 | Loop Genomics San Diego, CA Research Associate I, Biochemistry, Enzymes & Reagents B.S. degree in biology, molecular or cell biology, biochemistry, biological physics, bioengineering, chemical engineering, or equivalent field of stud Exp: 0-2+ years |
The Reagent Development group is seeking a Research Associate to assist with ongoing preparation of product for market and R&D of new sequencing biochemistry. In this position, candidates will carry out assays to assist in better understanding our reagents to improve the data quality and customer experience. Candidates are expected to be familiar with common laboratory techniques and be eager to learn under the direction of scientists. With mentoring, candidates will be able to develop and optimize methods and techniques for the testing and evaluation of cutting-edge sequencing reagents. | 12/9/2022 |
| 5637 | Loxo Oncology Louisville, CO Research Associate/Associate Scientist, Biophysics BS or MS Exp: 0-3+ years |
The ideal candidate is self-motivated, responsible, and a productive scientist who enjoys collaborating with biologists, chemists, and assay scientists. In this role, he/she will utilize a variety of assay technologies including mass spectrometry, fluorescence spectroscopy, surface plasmon resonance, and isothermal titration calorimetry to evaluate protein/ligand interactions. Experience in protein purification and characterization is a plus. This position requires excellent people skills, a positive can-do attitude, passion for lab work, attention to detail, and the ability to thrive in a highly interactive, fast-paced, team environment. | 12/9/2022 |
| 5638 | Loxo Oncology South San Francisco, CA Research Associate, Proteomics BA/BS, MS in Chemistry, Biology, Biochemistry, or related field Exp: 0-3+ years |
This position is an opportunity to learn and grow within a dynamic discovery biology team dedicated to creating specific targeted therapeutics for genetically defined oncology targets. The ideal candidate is someone who enjoys technical challenges, has the protein handling and cell culture skills needed to drive basic oncology research forward, and will excel in a collaborative environment. Experience with cell culture and biochemical techniques will be critical. Direct experience with sample preparation and method development for mass spectrometry are desirable. The ideal candidate will be enthusiastic about cancer research and is not afraid to get their hands dirty by helping with core lab functions including cell culture, protein characterization, mass spectrometry, and laboratory automation. The qualified candidate will have experience with basic chemistry/biology laboratory practices and is passionate to learn additional techniques working in a growing and dynamic group focused on discovery research. The candidate will work as part of a collaborative team of scientists with expertise in protein characterization, cell culture, chemistry, biochemistry, structure, and biophysics, supporting hit-to-lead and lead-ID phases of our oncology drug programs. The candidate will have opportunities to learn cutting edge techniques and to learn and develop technical expertise in proteomics. | 12/9/2022 |
| 5639 | Lonza Portsmouth, NH Quality Control Analyst, Microbiology BS, AA in Microbiology, Biochemistry or Related Science Exp: 0 yrs |
The QC Analyst will act as a team member of the Quality Control department to support production of in-process and final product drug lots for customers. The QC Microbiology Analyst should be able to provide on-time, high quality results to meet Manufacturing demands. *Shift : Weds-Sat 8PM-6:30AM* *Training will be conducted during the day shift for a few weeks *While working 3rd shift, the employee will receive a 20% shift differential *While working on any Saturday or Sunday, this employee will receive an additional 5% shift differential | 11/28/2022 |
| 5640 | Lonza Portsmouth, NH Quality Control Analyst, Environmental Monitoring Nights BS, AA in Microbiology, Biochemistry or Related Science Exp: 0 yrs |
As our QC Environmental Monitoring Analyst, you will support routine environmental monitoring of air, surface and clean utilities for manufacturing of in process and final product drug lots for customers. This position has a rotating 2-3-2 NIGHTS schedule (on 2 days, off 2 days, on 3 days) 7PM-7AM; While working this shift, the employee will receive a 20% shift differential; While working on any Saturday or Sunday, this employee will receive an additional 5% shift differential | 11/28/2022 |
| 5641 | Culture Biosciences South San Francisco, CA Bioprocessing Associate, Cell Culture Bachelor’s degree in Biology, Microbiology, Chemical Engineering, Biotechnology or a science related background. Exp: 1-2 years |
We are looking for a Bioprocess Associate with a cell culture background to help run our cloud biomanufacturing facility. Your work will contribute to getting novel biotechnology products to market faster and more efficiently. Your job will be to work as part of a team of bioprocess associates, engineers and project leads to execute key customer projects. In particular, you will learn mammalian cell culture techniques and work with state-of-the-art robotics, software, and automation equipment. | 11/28/2022 |
| 5642 | Cyprotex Watertown, MA Research Assistant BS/ MS in a relevant bio scientific discipline Exp: 0-2 years |
The team is looking for a highly motivated Research Associate and/or Research Assistant that will be responsible for routine screening of compounds in various in vitro toxicology assays | 11/28/2022 |
| 5643 | Cytovance Biologics Oklahoma City, OK QA Operations Associate I Bachelor’s Degree with emphasis on physical or life sciences Exp: 0 to 2 years |
QA Operations Associate I is responsible for maintaining quality oversight of operational areas by working closely with Operation’s personnel and performing various checks during manufacturing processes to ensure that current Good Manufacturing Practices (cGMP’s) are followed. The QA Operations Associate I also assess regulatory and quality risks in activities and processes according to GMP and Cytovance Standard Operating Procedures. | 11/28/2022 |
| 5644 | Day Zero Diagnostics Boston, MA Laboratory Technician Bachelor's degree in a chemical, physical, biological, or clinical laboratory science from an accredited institution, or a medical or biotechnology d Exp: 1 year |
Perform and assist with sample processing toward diagnostic workflows Execute repetitive workflows and strictly follow lab SOPs for specimen handling, processing, and reporting Ensure quality control of clinical samples and able to identify problems that may adversely affect test performance or test result reporting and notifying the appropriate supervisor Maintain meticulous documentation on sample processing and tracking, QC checkpoints, and any corrective actions taken when tests deviate from the laboratory’s established specifications | 11/28/2022 |
| 5645 | Exponential Business & Technologies Eden Prairie, MN Nano Analytical and Testing Lab Technician BE or BS degree in Materials Science and Engineering, Mechanical Engineering, Physics, Chemistry or related disciplines Exp: One to two years |
Ebatco is seeking an energetic, self-disciplined, customer service oriented technical person to join its Nano Analytical and Testing Laboratory (NAT Lab). As a technical member of the NAT Lab team, the technician performs contract lab services and instrument demonstrations with appropriate levels of support and supervision, operates advanced nano/micro scale scientific instruments, collects testing and measurement data, and writes technical report on experimental results and observations. | 11/28/2022 |
| 5646 | Editas Medicine Cambridge, MA Research Associate, In Vivo Pharmacology & Toxicology - 2168 BS/MS biology or related field Exp: 0-2 or 2+ years |
The In Vivo Gene Editing Department at Editas Medicine is looking to add a talented Research Associate to the Pharmacology & Toxicology group. This person will support routine in vivo research studies. The ideal candidate will have the ability to design and execute in vivo experiments using molecular based assays and have experience with various analytical testing methods (ddPCR, qPCR, ELISA, etc.). This individual will get to play a key role in advancing the next generation of pipeline programs at Editas. | 11/28/2022 |
| 5647 | Elektrofi Boston, MA Associate Scientist BS in Pharmaceutical Sciences, Chemical Engineering, Chemistry, Biology, Bioengineering, or a related field Exp: 0-2 years |
Elektrofi is looking for an Associate Scientist to support a team responsible for the development of platform formulations for Elektrofi’s proprietary microparticle production process. The candidate will support ongoing activities towards the development of Elektrofi’s biologics formulation platform. This individual will join an early-stage, multidisciplinary team of scientists and contribute to a variety of formulations activities in a highly collaborative environment. | 11/28/2022 |
| 5648 | Elektrofi Boston, MA Engineer I/II B.S. in Mechanical, Chemical, Biomedical, or Materials Engineering, Chemistry, Physics, or a related engineering discipline Exp: up to 2 years’ |
Elektrofi is looking for an Engineer I/II to support manufacturing, process development, or drug product development in the manufacturing and analysis of biologically active microparticle suspensions and their interactions with delivery devices. This individual will join a growing, multidisciplinary team of scientists and engineers and contribute to a variety of manufacturing and process development activities in a highly collaborative environment. | 11/28/2022 |
| 5649 | Elektrofi Boston, MA QC Analyst B.S. in Chemistry, Pharmaceutical Sci. or other relevant discipline Exp: entry-level |
Elektrofi is looking for an QC Analyst to join a team responsible for the qualification, validation and execution of method standard operating procedures (SOPs) to analyze biologically active microparticles. The successful candidate will perform routine testing panels for materials, intermediates, and test articles to support pre-clinical studies. This individual will join an early-stage, multidisciplinary team of scientists and engineers and contribute to a variety of CMC activities in a highly collaborative environment. | 11/28/2022 |
| 5650 | Element Biosciences San Diego, CA Research Associate, System Integration BS degree in chemistry, physics, molecular biology, bioengineering or similar field Exp: 1+ years |
This role will be responsible for key integration activities including running experiments cross-functionally, designing and executing component- and system-level tests and simplifying product workflows. While supported by teams of experts, the ideal candidate is a generalist at-heart and be comfortable learning and working in diverse disciplines including hardware, software, molecular biology and biochemistry. Your efforts will significantly contribute to a suite of products and improvements that will help shape the future of biology and change how we evaluate and measure both health and disease. | 11/28/2022 |
| 5651 | Element Biosciences San Diego, CA Research Associate I, Biochemistry, Enzymes & Reagents B.S. degree in biology, molecular or cell biology, biochemistry, biological physics, bioengineering, chemical engineering, or equivalent field of stud Exp: 0-2+ years |
The Reagent Development group is seeking a Research Associate to assist with ongoing preparation of product for market and R&D of new sequencing biochemistry. In this position, candidates will carry out assays to assist in better understanding our reagents to improve the data quality and customer experience. Candidates are expected to be familiar with common laboratory techniques and be eager to learn under the direction of scientists. With mentoring, candidates will be able to develop and optimize methods and techniques for the testing and evaluation of cutting-edge sequencing reagents. | 11/28/2022 |
| 5652 | EMD Serono St Louis, MO Associate Scientist - Quality Control Bachelor’s Degree in Chemistry, Biochemistry, Biology, Chemical Engineering, or other Life Science discipline Exp: 0+ years |
The Associate Scientist will evaluate assay products according to established protocols and contribute to the support functions to maintain group and department operations. The primary focus of this role is delivery of final assay results. | 11/29/2022 |
| 5653 | EMD Serono Carlsbad, CA Manufacturing Technician II- Cleanroom Bachelor’s Degree in Chemistry, Biochemistry, Biology, or other life science field Exp: 1+ years |
We are offering a $5,000 sign-on bonus for those that qualify. The Manufacturing Technician II position will work in a cleanroom environment and will follow cGMP batch records and SOPs to manufacture viral vector products (including cGMP biopharmaceutical cell culture, buffer and medium preparation, membrane clarification, membrane concentration, and buffer exchange, column purification, terminal filtration, Fill and Finish, stocking supplies and raw materials, and cleaning process equipment). Employees will support projects in conjunction with other GMP Manufacturing personnel (Leads, Supervisors, Managers). Employees will prepare suites for manufacturing, to document deviations, and to operate in a safe and compliant manner. The employee will be self-motivated, work well in a group, and communicate well with all levels of the operations team. | 11/29/2022 |
| 5654 | EMD Serono St Louis, MO Quality Assurance Associate Bachelor’s degree in Chemistry, Biology, or other Life Science field Exp: 0+ years |
At MilliporeSigma, the Quality Assurance Associate provides compliance oversight across the MilliporeSigma Quality Management System (QMS) in collaboration with site personnel. As a QA Specialist you are responsible for the implementation and maintenance of Quality Systems and processes to ensure internal and external compliance and the promotion of quality practices that meet or exceed required guidelines and regulatory requirements. Responsibilities include maintenance and continuous improvement of the overall Quality Program. | 11/29/2022 |
| 5655 | EMD Serono Tamaqua, PA CHE Engineer - ELDP Bachelor’s degree in Chemical Engineering Exp: 1+ years |
The Engineering Leadership Development Program (ELDP) provides a unique opportunity for highly talented and motivated recent graduates to gain valuable experience and training in the multifaceted disciplines of Semiconductor Materials operations. You may work in a production facility developing next generation CMP slurries, ultra-thin dielectric and metal film precursors, or formulated cleans and etching products to serve the semiconductor industry. During the program, members will experience three, 12-month rotational assignments, while receiving exposure to the company's core businesses, processes, technologies, and leaders. The rotations will take place in diverse functions such as Production, Supply Chain, Quality, and Engineering. | 11/29/2022 |
| 5656 | EMD Serono Tamaqua, PA ELE Engineer - ELDP Bachelor’s degree in Electrical Engineering Exp: 1+ years |
The Engineering Leadership Development Program (ELDP) provides a unique opportunity for highly talented and motivated recent graduates to gain valuable experience and training in the multifaceted disciplines of Semiconductor Materials operations. You may work in a production facility developing next generation CMP slurries, ultra-thin dielectric and metal film precursors, or formulated cleans and etching products to serve the semiconductor industry. During the program, members will experience three, 12-month rotational assignments, while receiving exposure to the company's core businesses, processes, technologies, and leaders. The rotations will take place in diverse functions such as Production, Supply Chain, Quality, and Engineering. | 11/29/2022 |
| 5657 | EMD Serono Tempe, AZ Analytical Chemist Master’s degree in Chemistry, Biochemistry, or other Scientific discipline Exp: 1+ years’ |
EMD Electronics in Tempe, AZ is seeking an Analytical Chemist to perform laboratory operations including chemical and physical analysis. | 11/29/2022 |
| 5658 | Millipore Tamaqua, PA MeE Engineer ELDP Bachelor’s degree in Mechanical Engineering Exp: 1+ years |
The Engineering Leadership Development Program (ELDP) provides a unique opportunity for highly talented and motivated recent graduates to gain valuable experience and training in the multifaceted disciplines of Semiconductor Materials operations. You may work in a production facility developing next generation CMP slurries, ultra-thin dielectric and metal film precursors, or formulated cleans and etching products to serve the semiconductor industry. During the program, members will experience three, 12-month rotational assignments, while receiving exposure to the company's core businesses, processes, technologies, and leaders. The rotations will take place in diverse functions such as Production, Supply Chain, Quality, and Engineering. | 11/29/2022 |
| 5659 | Millipore St Louis, MO Scientist, Molecular Biology And Microbiology Bachelor's degree in a Life Science Exp: 1+ year(s) |
The role is responsible for supporting the Technical Leader, as an extended project team member, supporting product development and improvement projects, customer applications, as well as R&D and Marketing activities. | 11/29/2022 |
| 5660 | Millipore Carlsbad, CA Specialist II, Analytical Development Master’s Degree in chemistry, Biochemistry, Biology, or similar life science discipline Exp: 1+ years |
MilliporeSigma is seeking a motivated Specialist II- Analytical Development to join its dynamic and collaborative process development team at the Carlsbad viral vector CDMO facility. The successful candidate will play a key role in developing analytical methods to support viral vector process development activities, including method qualification and validation activities. The candidate will also act as a driver for continuous advancement in viral vector analytical science and operational excellence across functions. | 11/29/2022 |
| 5661 | Millipore Rocklin, CA Histology Lab Manufacturing Technician Bachelors’ Degree in Chemistry, Biology, or other Biological Science discipline. Experience using a microtome. Exp: 1+ years’ |
At MilliporeSigma, the Histology Lab Manufacturing Technician is responsible for performing Histology related functions. This includes microtomy, staining of tissue by immunohistochemistry (IHC), tissue processing and embedding. The ideal candidate has experience using a microtome and is eager to work as a team to meet departmental goals and deadlines. This position reports to the Manufacturing Supervisor as part of the Operations team located at the Rocklin Site, where we manufacture products for use in in vitro diagnostic (IVD) IHC. | 11/29/2022 |
| 5662 | Millipore Allentown, PA Process Engineer MS degree in Chemical Engineering Exp: 0-3 years |
At EMD Electronics, a Process Engineer in the Integrated Supply Chain (ISC) Process Engineering group, you will collaborate with project management and EPC contractors as the responsible engineer for all process design questions. You will also interact very closely with site operations, process safety, and the process development group in the execution of the responsibilities of this position. | 11/29/2022 |
| 5663 | Millipore Milwaukee, WI Associate Production Scientist Bachelors Degree in Chemistry, Biochemistry, Biology, Chemical Engineering, or other Life Science field Exp: 1+ year |
Manufacture, package, and evaluate products according to established protocols, provide technical support to others, lead safety initiatives & projects, and perform operations in support of the group and department. This is a 3rd shift position with regular scheduled work hours of 10:00pm-6:30am Sunday – Friday but may occasionally differ depending on business needs. | 11/29/2022 |
| 5664 | Endo Pharmaceuticals Rochester, MI Process Engineer I BS degree in Engineering or Chemical Engineering OR MS Exp: BS: 0-3+ years’ ; MS: 0-1+ year |
The Process Engineer I, with guidance, performs various duties related to optimization and analysis of production processes, new products, processes and technology transfers. Prepare and execute engineering study protocols, manufacturing and packaging experimental / feasibility study / validation batch records and protocols and complete interim and / or final summary reports for marketed and new products. Perform or assist on-site and site-change technical transfer, scale-up or scale-down factor evaluation, manufacturing / packaging process and equipment troubleshooting, and SOP preparation and review. | 11/30/2022 |
| 5665 | Endo Pharmaceuticals Rochester, MI Associate Process Engineer, Set-up Specialist - Afternoon Shift Bachelor’s Degree or higher in Engineering or Science related equivalent, preferred. Exp: 1-3 years’ |
The Associate Process Engineer, Set-up Specialist, works in a hands-on capacity in a fast-paced, cGMP environment and production support areas to process sterile and aseptic products. The specialist works in collaboration with Operations, Maintenance, Engineering and Validation for successful repeatable day-to-day manufacturing operations. The role operates and supports one or more of these manufacturing departments: Formulation, Filling, Inspection, Packaging. | 11/30/2022 |
| 5666 | Endo Pharmaceuticals Rochester, MI Chemist II (Afternoon Shift) Master’s Degree in chemistry, chemical engineering or related field Exp: 1+ years’ |
The Chemist II, under general supervision, performs QC laboratory chemical analyses of raw materials, in-process materials, stability and finished products, and testing to support process validation. Detects, participates and reports on OOS/OOT/NOE and other investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. May train less senior staff. | 11/30/2022 |
| 5667 | Enzo Life Sciences Farmingdale, NY Technologist (Chemistry) Bachelors Degree in Clinical Laboratory Science, Medical Technology or related degree, preferred Exp: one (1) year |
The technologist will perform qualitiative and quantitative tests and examinations using various analyzers and/or manual methods. Assist in performing established quality assurance procedures (quality control testing, instrument function checks and calibrations). Maintains appropriate documentation and reports irregularities. Shift: 10:00PM - 6:30AM (Flexible Hours and receive a sign-on bonus) | 11/30/2022 |
| 5668 | Enzo Life Sciences Farmingdale, NY Technologist (Molecular) Bachelors Degree in Clinical Laboratory Science, Medical Technology or related degree, preferred Exp: one (1) year |
The technologist will perform qualitative and quantitative tests and examinations using various analyzers and/or manual methods. Assist in performing established quality assurance procedures (quality control testing, instrument function checks and calibrations). Maintains appropriate documentation and reports irregularities. Evening Shift: Tues-Sat 3:00pm-11:30pm and alt weekends as needed | 11/30/2022 |
| 5669 | Enzo Life Sciences Farmingdale, NY Associate Scientist Bachelor’s or Master’s Degree in Chemistry or other scientific field. Exp: 1+ years |
Working under the direct supervision of the Director of Chemistry, this position is responsible for the synthesis, purification, and quality control of small molecule compounds and other chemistry products. | 11/30/2022 |
| 5670 | Exelixis Alameda, CA Scientist II - Tumor Biology MS/MA degree in related discipline Exp: one year |
We are looking for a Scientist to join our Tumor Biology group. The successful candidate will have prior experience to evaluate the activity of small molecules in cell-based assays for oncology drug discovery. The successful candidate will also have prior experience with isolation and culture of cancer-associated fibroblasts (CAF) and tumor/stromal cell in vitro co-culture system for modeling the in vivo stromal compartment in the tumor microenvironment. Comfortable in a dynamic and energetic team-based environment, the ideal candidate will reliably execute experiments, interpret and analyze results. Good lab practicing and multitasking are required. This job will require the candidate to have good organization, communication and teamwork skills as well as flexibility and versatility to meet tight deadlines in a dynamic, fast-moving environment. | 11/30/2022 |
| 5671 | Exelixis Alameda, CA Scientist III MS/MA degree in related discipline Exp: one year |
We are looking for a Scientist to join our Tumor Biology group. The successful candidate will have prior experience to evaluate the activity of small molecules in cell-based assays for oncology drug discovery. The successful candidate will also have prior experience with isolation and culture of cancer-associated fibroblasts (CAF) and tumor/stromal cell in vitro co-culture system for modeling the in vivo stromal compartment in the tumor microenvironment. Comfortable in a dynamic and energetic team-based environment, the ideal candidate will reliably execute experiments, interpret and analyze results. Good lab practicing and multitasking are required. This job will require the candidate to have good organization, communication and teamwork skills as well as flexibility and versatility to meet tight deadlines in a dynamic, fast-moving environment. | 11/30/2022 |
| 5672 | Exelixis Alameda, CA Assoc Scientist Bachelor’s degree in chemistry, biochemistry, pharmaceutical sciences or related field Exp: one year |
The lab operations supervisor will assist the CMC team by managing the daily activities in the lab. The successful candidate will be highly motivated, have strong communication skills, be resourceful and well organized. | 11/30/2022 |
| 5673 | Exelixis Alameda, CA Scientist I (Pharmacology) MS degree in related discipline Exp: zero to two years |
The hands-on Scientist I (Pharmacology) will support the in vivo pharmacology research program and contribute to the multidisciplinary research team by designing and executing in vivo studies for pharmacokinetics and toxicology. The successful candidate will be a highly creative scientist with a strong desire to succeed at the highest level. | 12/1/2022 |
| 5674 | Fresenius Kabi Melrose Park, IL Manufacturing Engineer - Packaging (Fri, Sat, Sun Nights) Bachelor’s degree in Engineering (Electrical, Mechanical, Automation, Controls, Computer, etc.). Exp: 1-3 years |
Manufacturing Engineer - Packaging is responsible for using technical expertise in support of daily operations in packaging operations by defining, measuring, analyzing, coordinating, implementing and follow-up concerning projects and activities designed to increase or improve safety, quality, productivity, and/or capacity. Apply accepted engineering practices and project management techniques to assigned daily tasks and projects. Analyze situations, break them down into key components and milestones, conduct fact-finding missions, provide detailed plans of action, and implement plans as assigned. | 12/1/2022 |
| 5675 | DVC LLC Silver Spring, MD Research Assistant BS in Biology, Microbiology, Medical Technology or related field Exp: 1+ years |
This position would provide support to the NMRC IDD Wound Infections Department by carrying out laboratory research procedures for working with multidrug resistant bacteria causing traumatic wound infections. | 12/1/2022 |
| 5676 | Genentech Seattle, WA Research Associate Doctorate, Master’s or Bachelor’s degree in Molecular biology, Protein Engineering, Bioengineering, Biochemistry or related field Exp: 1 year |
After training on our current work processes and established SOPs, execute defined sequencing experiments that advance research and development efforts on our multifaceted nanopore-based sequencing platform. • Use technical and theoretical understanding to explain experimental findings while keeping experimental protocols and data well organized and documented. • Communicate actively, effectively, and promptly with manager on project status, data analysis findings, experimental observations, and process deviations. • Support management decisions and goals in a positive, professional manner. Embrace priorities and responsibilities set forth by management. • Analyze and interpret experimental data using various data analysis software (e.g., Excel, Python) and/or applying quantitative methods. • Prepare clear data summaries that include conclusions and follow-up steps to review with manager. When needed, effectively present findings to team members. | 12/1/2022 |
| 5677 | Genentech Indianapolis, IN QUALITY CONTROL TECHNICIAN - DIABETES CARE (2ND SHIFT, CONTRACT) Bachelor’s degree in technical or scientific field or equivalent experience Exp: 1+ years’ |
Perform analyses finished product from other sections of manufacturing or performs investigations according to established procedures to determine conformance to acceptance specifications for a particular chemical or physical property. Prepares instruments and apparatus according to established procedures to support the testing activities of the unit. May monitor and verify quality in accordance with statistical process or other control procedures. | 12/1/2022 |
| 5678 | Genentech Hillsboro, OR QUALITY CONTROL TECHNICIAN (CONTRACTOR) B.A. or B.S. degree (preferably in Life Science) Exp: 1-3 years |
Responsibilities include performing and reviewing a variety assays in the Quality Control organization in support of In-Process intermediates, drug substance, drug product and stability sample testing in a cGMP environment. The QC Technician must be able to interpret data troubleshoot assay failures and equipment issues while adhering to strict guidelines on cGMP documentation. In addition, the individual will support cycle development, performance qualifications, method transfers, discrepancy/out of specification investigations and collaborate with external groups to identify improvement opportunities in technology and business process. Shift: Sunday to Wednesday or Wednesday to Saturday, 4x10’s Day: 6:30am to 5:00pm Swing 11:30am to 10:00pm Contract duration: 12 months with possible extension up to 3 years | 12/1/2022 |
| 5679 | Genentech South San Francisco, CA SCIENTIST 2/3, PROCESS DEVELOPMENT AND OPTIMIZATION, SMALL MOLECULE PROCESS CHEMISTRY MS in Chemical Engineering or Chemistry. Exp: 1+ years |
Genentech, a leader in bio-pharmaceutical sciences, is seeking a highly-motivated and talented researcher with a proven track record of laboratory achievements to join our growing Department of Small Molecule Process Chemistry. | 12/1/2022 |
| 5680 | Genentech Hillsboro, OR ENGINEER II/SENIOR ENGINEER, MAINTENANCE B.S or higher in Chemical, Biochemical, Electrical or Mechanical Engineering or related discipline Exp: 1-5+ years |
Collaborate with management to establish priorities, milestones and targets. Represent the department functionally, cross functionally and cross site for various activities and initiatives applying discretion to independently address issues or resolve problems. Facilitate and/or participate in various activities such as gap analysis and root cause analysis. Provide technical support for instrumentation and maintenance related activities associated with manufacturing equipment / systems, Tank Management, and Critical GMP utility systems located at the Genentech Hillsboro Technical Operations fill finish facility. Provide technical writing assistance for Instrumentation and maintenance support documentation and changes. | 12/1/2022 |
| 5681 | BioVision Fremont, CA Research Associate/Sr. Research Associate BS Degree in biochemistry, pathology, cell and molecular biology, immunology or other Life Sciences. Exp: 0-3 years |
Focus on the development and validation of qualified antibodies for IVD immunohistochemistry (IHC) applications under FDA and MDSAP/ISO13485 (2016) quality standards. | 11/21/2022 |
| 5682 | Blueprint Medicines Cambridge, MA Associate Scientist, Biology MS in oncology, cellular biology, molecular biology, or related discipline Exp: 1-3 years |
This position offers the opportunity to impact a growing portfolio of targeted therapies in a fast-paced and innovative research environment. We are searching for a dynamic Associate Biology Scientist with experience interrogating cellular and molecular mechanisms as they relate to kinase target pathway modulation, off-target liabilities, and resistance. | 11/21/2022 |
| 5683 | Cambrex Charles City, IA Chemical Development Scientist I M.S. in Chemistry or related field Exp: no experience |
Position is directed toward optimization of existing chemical routes and development of alternate chemistry toward key synthetic intermediates and APIs. Carries out multistep chemical synthesis and product isolation/purification operations in the laboratory, independently or as part of an integrated team. Chemist utilizes modern analytical tools to determine identity and purity of products made during projects. Communication with clients in regular team meetings; prepares R&D reports at the conclusion of projects. | 11/23/2022 |
| 5684 | Cambrex Agawam, MA QA Specialist I Related BA/BS degree Exp: 0-2+ years |
The QA Specialist I supports the Quality Management System (QMS) and the Document Management System (DMS) in a GMP regulated environment according to established operating procedures. The QMS and DMS functional areas include but are not limited to: Document Control, Training, Deviations, Out of Specification Investigations, Corrective and Preventive Actions (CAPA), Change Control, Complaints, Quality review of analytical and microbiological data and batch production records, Internal Audits, Supplier/Subcontractor Management, Validation, and Calibration & Maintenance. | 11/23/2022 |
| 5685 | Advanced Sterilization Products Skillman, NJ Scientist I, Skin Health R&D PPI Body Master’s degree in Chemistry, Chemical Engineering, Industrial Pharmacy, material science or other science or engineering discipline is preferred. Exp: 0-1 years |
The Scientist will support the product development of regional and global projects for new Body Moisturizers and Cleansers. He or she will work closely with their manger and team to understand how to improve and build on our Body pipeline initiatives. They will also partner closely with all functions responsible for launching a product to help assess risk, understand, and proactively solve for potential hurdles to ensure successful new product launches. Responsibilities and primary duties include formulation prototype development and batching, including stability and consumer evaluation, attending project update meetings and project related documentation. Excellent communication skills together with the ability to manage complexity are must-have prerequisites. | 11/24/2022 |
| 5686 | Advanced Sterilization Products Brisbane, CA Associate Scientist, in Vitro Assays Gene Therapy Discovery M.S. Exp: 1 year |
We are seeking a highly motivated and independent Associate Scientist to join a group that is developing in vitro assays to characterize the functional activity and potency of therapeutic proteins delivered via adeno-associated virus (AAV) or other viral vectors to HEK293 cells and disease cell models. The qualified scientist should have experience working in the field of gene therapy and technical expertise with in vitro functional assays and mammalian cell culture, AAV transduction, and in vitro functional assays. The scientist will plan and execute experiments, follow protocols, interpret data, troubleshoot problems, document data, and communicate results, while working in a collaborative environment that values innovation, leadership, scientific excellence, and personal accountability. | 11/24/2022 |
| 5687 | Advanced Sterilization Products Skillman, NJ Assistant Scientist, Skin Health & Beauty Bachelor’s degree Exp: 1-3 years |
The R&D Skin Health and Beauty Assistant Scientist will lead new product launches and life cycle management for Skin Health and Beauty products, with a focus on the Facial Moisture category. This person will be expected to develop and demonstrate expertise in product and process development. Working cross-functionally, they will be a key member working end-to-end to launch a product and maintain it through its life cycle. Responsibilities and primary duties include formulation prototype development, product robustness and consumer evaluation, attending project meetings, and creation of supporting documentation. Excellent interpersonal skills together with the ability to handle complexity are must-have prerequisites. | 11/24/2022 |
| 5688 | Catalent Baltimore, MD Associate Scientist III M.S. in Chemical Engineering, Chemistry, Biochemistry, Life Sciences Exp: 1-3 years |
The Associate Scientist III functions independently and is actively engaged in process and product development within a dynamic project team with supervision. Displays strong technical knowledge, initiative and scientific commitment, and makes significant scientific and technical contributions to downstream process development within the Pre-Clinical Downstream Development Group. Work Schedule: 9am-5pm or 10am-6pm | 11/24/2022 |
| 5689 | Catalent Chelsea, MA Quality Control Analyst - Microbiology Bachelor’s?Degree?in life sciences or a related field?required.? Exp: 1 year |
Catalent Pharma Solutions is Chelsea, MA is hiring a Quality Control Analyst, Microbiology who is responsible for Environmental Monitoring sampling, analyzing, and microbiological testing to support GMP manufacturing. They will conduct routine and non-routine environmental and utilities monitoring and perform microbial testing of samples according to standard operating procedures. The Quality Control Analyst compiles data for documentation of test procedures, participates in the preparation of investigations, summaries and reports, and reviews data obtained for compliance to specifications and reports out-of-trend and/or out-of-specification results. | 11/24/2022 |
| 5690 | Catalent Morrisville, NC Associate Scientist - CONVERSION Bachelor’s Degree in chemistry or closely related physical science Exp: 1-3 years |
Execute laboratory work plan/schedule developed with input from supervisor or senior team member May draft technical documents such as methods or certificates of analysis Performs parallel review of laboratory documentation and may become qualified to perform technical review of documents for accuracy, thoroughness and regulatory compliance Trains others on laboratory techniques Assists in the execution of efficiency improvement project with guidance | 11/24/2022 |
| 5691 | Catalent Morrisville, NC Scientist Master’s degree Exp: 1-2 years |
Execute laboratory workplan/schedule developed with input from supervisor or senior team member May draft technical documents such as methods or certificates of analysis Performs parallel review of laboratory documentation and may become qualified to perform technical review of documents for accuracy, thoroughness, and regulatory compliance Trains others on procedures and laboratory techniques Executes efficiency improvement project with guidance | 11/24/2022 |
| 5692 | Catalent Baltimore, MD Associate Scientist III M.S. in Molecular Biology, Chemistry, Biology, Life Sciences, or related field Exp: 1-3 years |
Catalent Cell and Gene Therapy is looking to recruit an Associate Scientist III to join our growing team in Baltimore, MD. The Associate Scientist III functions independently and productively as an Analytical Scientist and is actively engaged in the process and product development within a dynamic project team. Displays strong technical knowledge, initiative, and scientific commitment, and makes significant scientific and technical contributions within the Process Development Group. Serves as a technical lead and interacts with clients and Supervisors to ensure project goals are met. | 11/24/2022 |
| 5693 | Catalent Kansas City, MO Associate Scientist II - Bio Separations Bachelor's degree in life sciences such as chemistry, biochemistry, biology or closely related physical science required Exp: 0-3+ years |
Catalent Pharma Solutions in Kansas City, MO is hiring an Associate Scientist II for our Biologics II Team. The main activities will be to provide and report data, as required by project contracts within the Biologics Department. The data may be used for submission in Regulatory packages, release and stability testing of clinical and animal trial dose forms and in support of development projects. This is a full-time role position: Monday – Friday, days.\ | 11/24/2022 |
| 5694 | Cayman Chemical Ann Arbor, MI Associate Scientist I - ELISA R&D Master's degree in Life Sciences or Chemistry preferred Exp: 1-year |
Assist in development of new ELISA’s, including but not limited to: immunogen and tracer development, antibody/antisera characterizations, formulation and stability testing, sample analysis, and validations Help prepare and maintain Laboratory SOPs and product inserts General upkeep of the lab and maintenance of laboratory equipment and raw materials inventory Keep complete, current, and accurate records of all experiments, techniques, procedures, and results in a laboratory notebook Reads scientific literature with accuracy and understanding; keywords articles as needed Utilize resources including but not limited to EndNote, PubMed, and journal articles Reports status of work to supervisor regularly, i.e. weekly updates, monthly report, etc. Present project updates at group and departmental meetings | 11/24/2022 |
| 5695 | Celldex Therapeutics Hampton, NJ Assistant Scientist BS/BA degree or Associates Degree with experience in related field. Exp: 0-2+ years |
The Assistant Scientist provides daily care of research animals for experimental purposes, including performing basic husbandry duties. Responsible for maintenance of the Animal Facility including regular facility sanitation. Performs in vivo research support duties such as sample collection, data collection, treatment dosing, and can develop new skills as required based on research needs. In addition, the Assistant Scientist will be responsible for planning their schedule to assist with in vitro assays and cell culture. | 11/24/2022 |
| 5696 | Cerus Concord, CA Engineer I or II (hybrid) Master’s degree in chemical, mechanical, or biomedical engineering Exp: 0-2+ years |
Provide laboratory and engineering support for the Class III INTERCEPT Blood System for Platelets and Plasma. Focused primarily on new product development, manufacturing product and quality improvements, supply chain assurance, and margin expansion projects. Includes laboratory testing of and for single-use INTERCEPT Processing Sets and components thereof. | 11/25/2022 |
| 5697 | Champion Oncology Rockville, MD Research Technician II, Study Services BS/MS degree in biology, pharmacology, or related field Exp: 1 year |
As a Research Technician in Study Services, you will support in vivo oncology studies in mice. Additional duties and responsibilities include: Perform in-life technical procedures, handle, restrain, and provide care for all animals; Observe animals for general health and overall well-being Administer therapeutic agents by various routes; Provide animal welfare assessments, including body weight and tumor volume measurement Allocate animals to study and non-study groups; Provide preoperative animal care; Euthanize animals as directed in study protocols and directives; Read study protocols and extract pertinent information; Perform study preparation activities including collection tube labeling and room/BSC set-up Record data using laboratory information management systems; Work weekends and holidays on rotating basis | 11/25/2022 |
| 5698 | ChemGenes Wilmington, MA Senior Research Support Associate B.S. degree in Biochemistry, Biology or related field Exp: 0–2 years |
Manufacture of synthetic DNA & RNA compounds. Assist with experiments supporting research in the synthesis of single-cell-barcoded beads, quality control of the synthesized beads, and performing experiments that include basic molecular biology techniques to sequencing experiments to validate and troubleshoot synthesis of DNA oligos to beads. Provide comprehensive technical support for scientists in the company; executing and optimizing ongoing experiments, analyzing results and designing follow-up experiments based on the results, and presenting findings and insights at group meetings. Evaluating research methods, procedures and techniques based on established objectives, conceiving and designing basic experimental protocols to ensure project completion in a timely fashion; recording and organizing data generated from the experiments in clear, concise, and assessable format; perform basic coding and statistical analyses; processing of in-vitro and in-vivo RNA for preparation of RNA-seq libraries for sequencing in Illumina platforms (Mi-Seq including Hi-seq and Next-seq). Experienced in techniques including but not limited to: running agarose gel, polyacrylamide gel electrophoresis, reverse transcription, quantitative PCR, fluorescent microscopy, flow cytometry; maintaining inventories of lab stocks. | 11/25/2022 |
| 5699 | Cognate BioServices S. San Francisco, CA Research Associate I BS in the biological sciences or relevant area required. Exp: 0-3 years |
Explora BioLabs, an entity of Charles River, is seeking a Research Associate I located in San Francisco, CA. In this role, the incumbent will perform a variety of animal procedures to support company and client research projects (e.g., set up the study forms, set up the procedure rooms, label and ship samples, etc.). To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions | 11/25/2022 |
| 5700 | Cognate BioServices Mattawan, MI Research Analyst I - Formulations Bachelor’s/Master’s degree in a relevant field Exp: no experience |
We are seeking a Research Analyst I for our Test Material Control/Formulations Department site located Mattawan, MI. A Research Analyst I - Test Material Control (TMC)/Formulations is responsible for: preparing, sampling, and dispensing formulated test material according to applicable Standard Operating Procedures (SOPs) and GxP guidelines. The individual in this role: completes projects on time while maintaining quality and efficiency; communicates effectively with management, internal customers, and team members; assists others with their duties; and may assist with troubleshooting formulation issues. *Training will be performed Mon - Friday 6:00 AM - 2:30 PM. Following the completion of training standard working hours will be Friday - Monday beginning at 6:00 AM. Depending on assigned shift, additional hours could be required or requested during nights, weekdays, weekends and/or holidays. | 11/25/2022 |
| 5701 | Cognate BioServices Mattawan, MI Research Technician - Surgery and Efficacy - Surgery OR HS/GED/Bachelor's degree (preferred, not required) Exp: no experience |
Job Summary **$1,000 Sign-On Bonus*** **1st Shift Mon-Fri 700am-330pm** We are seeking an experienced Research Technician for our Surgery (OR) Team at our Safety Assessment site located in Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives.Job Summary | 11/25/2022 |
| 5702 | Cognate BioServices Boston, MA Surgical/Research Veterinary Technician - Position includes a $2,000 sign on bonus Bachelor’s degree (B.A./B.S.) or equivalent in animal science preferred. Exp: (6) months |
Help us contribute to beating pediatric cancers! Boston Children's Hospital is focusing research on finding cures for pediatric cancer and Charles River is looking for talented, caring and committed surgical veterinary technician to contribute to these life-saving efforts. | 11/25/2022 |
| 5703 | Cognate BioServices Mattawan, MI Research Analyst I - Formulations Bachelor’s/Master’s degree in a relevant field Exp: no experience |
We are seeking a Research Analyst I for our Test Material Control/Formulations Department site located Mattawan, MI. A Research Analyst I - Test Material Control (TMC)/Formulations is responsible for: preparing, sampling, and dispensing formulated test material according to applicable Standard Operating Procedures (SOPs) and GxP guidelines. The individual in this role: completes projects on time while maintaining quality and efficiency; communicates effectively with management, internal customers, and team members; assists others with their duties; and may assist with troubleshooting formulation issues. *Training will be performed Mon - Friday 6:00 AM - 2:30 PM. Following the completion of training standard working hours will be Friday - Monday beginning at 6:00 AM. Depending on assigned shift, additional hours could be required or requested during nights, weekdays, weekends and/or holidays. | 11/25/2022 |
| 5704 | Cognate BioServices Reno, NV Research Analyst I -Bio/Immunology 1 Bachelor’s degree (B.A. / B.S.) in biological science or related discipline preferred. Exp: 6 Months |
We are seeking a Research Assistant 1 for our Safety Assessment site located in Reno, NV. This position will be responsible for handling and processing samples, and performing accurate data collection and reporting. Basic methods will be used to perform laboratory tasks with minimal supervision in the performance of studies. | 11/25/2022 |
| 5705 | Companion Medical North Haven, CT Chemist I Bachelor’s degree in chemistry, biology, material science, or related technical discipline Exp: 0 years |
The chemist will be responsible for performing Non-volatile Residue (NVR) analysis, extractions and sample preparations in an analytical chemistry lab. The position has responsibility for executing chemical characterization test methods and protocols, including sample preparation, extraction studies and instrumentation setup. The role functions as part of an analytical chemistry team that works under ISO17025 and ISO 13485 requirements in the medical device field. | 11/25/2022 |
| 5706 | Companion Medical Santa Ana, CA Microbiologist-Sterilization I - Santa Ana, CA Bachelor's degree in science or a technical discipline Exp: 0 years |
In this exciting role as a Microbiologist-Sterilization I you will have responsibility for supporting on market product sterilization validations. You will have responsibility for sustaining sterilization work and to support of changes to existing products and introduction of new products. These validations include product sterilization validations, along with product and process validations. The position provides technical solution to achieve validated sterilization processes for new and existing products. Updates to routine sterilization procedures and related specifications. Supports and leads team with assessments of new products or changes to existing products. | 11/25/2022 |
| 5707 | Companion Medical Santa Rosa, CA Microbiologist-Steriliz I Bachelors degree required Exp: 0 years |
Responsibilities may include the following and other duties may be assigned. Analyzes chemical, biological or microbiological products, raw materials, in-process materials, release test samples or stability samples in support of the company's quality program. Prepares, cleans, disinfects, and/or sterilizes instruments, materials, products, and/or supplies. Follows protocols and regulations in order to clean, store, and/or deliver products, supplies, and/or instruments. Interprets and evaluates the analyses in terms of accuracy and precision compared against established specifications and recommends and implements corrective action where necessary. | 11/25/2022 |
| 5708 | Companion Medical Santa Ana, CA Microbiologist II Master's degree (Advanced) Exp: 0 years |
In this exciting role as a Microbiologist-Sterilization II you will have responsibility for supporting on market product sterilization validations. You will have responsibility for sustaining sterilization work and to support of changes to existing products and introduction of new products. These validations include product sterilization validations, along with product and process validations. The position provides technical solution to achieve validated sterilization processes for new and existing products. Updates to routine sterilization procedures and related specifications. Supports and leads team with assessments of new products or changes to existing products. | 11/25/2022 |
| 5709 | Companion Medical Rice Creek, MN Chemist II Advanced Degree in Chemistry or a related technical discipline Exp: 0+ years |
As a Chemist II, you will focus on supporting the Analytical Development initiatives to support new and existing technologies. This role requires effective collaboration, time management and prioritization of multiple concurrent tasks in a team focused environment. | 11/25/2022 |
| 5710 | Companion Medical Irvine, CA Microbiologist-Sterilization II - Irvine, CA Advanced degree in science or technical field Exp: 0+ years |
In this exciting role as a Microbiologist-Sterilization II you will have responsibility for supporting on market product sterilization validations. You will have responsibility for sustaining sterilization work and to support of changes to existing products and introduction of new products. These validations include product sterilization validations, along with product and process validations. The position provides technical solution to achieve validated sterilization processes for new and existing products. Updates to routine sterilization procedures and related specifications. Supports and leads team with assessments of new products or changes to existing products. | 11/25/2022 |
| 5711 | CooperSurgical Palo Alto/Los Altos, CA Laboratory Technician Bachelor's degree in Science preferred Exp: One to two years |
Position Summary: Performs routine semen banking procedures | 11/25/2022 |
| 5712 | CooperSurgical Livingston, NJ Laboratory Technician I Bachelor’s or Master’s Degree in Biology or other related science Exp: 1 year |
Position Summary: Performs complex molecular-based procedures on clinical samples. Analyzes clinical results and provides diagnoses. Performs clinical tasks associated with clinical cases | 11/25/2022 |
| 5713 | CooperSurgical Livingston, NJ Lab Technician I Bachelor's degree in the sciences OR a Master's degree in Biology or related science Exp: one year |
Position Summary: Performs complex molecular-based procedures on clinical samples. Analyzes clinical results and provides diagnoses. Performs clinical tasks associated with clinical cases. | 11/25/2022 |
| 5714 | CooperSurgical Livingston, NJ PGT-M Labratory Technologist Bachelor’s or master’s degree in Biology or other related science Exp: 1 year |
The PGT-M Laboratory Technologist performs complex molecular-based procedures on clinical samples. Analyzes clinical results and provides diagnoses. Performs clinical tasks associated with clinical cases. | 11/25/2022 |
| 5715 | CooperSurgical Los Angeles, CA Laboratory Technician I Bachelor's degree in Science preferred Exp: one to two years |
Position Summary: Performs routine semen banking procedures | 11/25/2022 |
| 5716 | CooperSurgical Cambridge, MA Laboratory Technician I Bachelor's degree in Science preferred Exp: one to two years |
Position Summary: Performs routine semen banking procedures | 11/25/2022 |
| 5717 | Contract Pharmacal Hauppauge, NY Chemist (Quality Control) Bachelor’s degree in Chemistry or related science required Exp: 1 to 9 years |
The Chemist, QC position is responsible for and has experience in performing chemical testing and completion of real-time documentation per cGMPs and current SOPs. | 11/25/2022 |
| 5718 | Crown Bioscience San Diego, CA Research Associate I - Biomarker & Diagnostic Tech Bachelor of Science degree or above in biotechnology, cell biology, immunology, oncology or other related disciplines Exp: one year |
The purpose of the Research Associate I position is to provide support on biomarker discovery studies to meet company's goals, objectives and quality standards. | 11/25/2022 |
| 5719 | Crown Bioscience San Diego, CA Research Associate I - Inflammation & Immunology Associate's degree or Bachelor's degree in Biology, Biotechnology or other relevant area of scientific discipline. Master's degree in biology in Biol Exp: 1-2 year(s) |
The purpose of the Inflammation and Immunology Research Associate I position is to perform primarily in vivo animal studies within the Inflammation and Immunology group in support of the Company's goals and objectives. | 11/25/2022 |
| 5720 | Crown Bioscience San Diego, CA Research Associate I, In Vivo Oncology Bachelor’s Degree in a scientific discipline Exp: One year |
In Vivo Research Associate I position is to provide support on In Vivo studies within the In Vivo Pharmacology group meeting Company's goals, objectives and quality standards. | 11/25/2022 |
| 5721 | Avantor Sciences Bridgewater, NJ Associate Scientist - Downstream MS degree in biochemistry, molecular biology, chemistry, cell biology, chemical engineering, or bioengineering Exp: 6 + months |
The Associate Scientist - Downstream will be responsible for the hands-on execution of laboratory experiments for the protein purification process and contribute to the development and optimization of processes. The primary responsibilities will include: • Executing and supporting downstream purification (e.g., monoclonal antibodies, fusion proteins, etc.) on a bench-scale jointly with other scientists or independently. • Conducting pilot-scale material generations with the team. • Preparing and executing experimental protocols and analytical test methods under general guidance. • Accurately documenting all procedures and observations • Maintaining laboratory area, utilizes safe practices while working in the laboratory environment as per EHS guidelines and policy. | 11/14/2022 |
| 5722 | Bardy Diagnostics Cleveland, MS Process Engineer I Bachelor Degree in Engineering Required (Mechanical, Industrial, Electrical, or Computer degrees are preferred) Exp: 1 or more years |
This position is a key role in the Injection Molding and Devices. Primary focus will be on implementing continuous improvement, new business, and capacity expansion projects. Additional focus will also be on manufacturing equipment reliability and process support work within the Injection Molding and Device Operations. Cross-functional project management will be involved in this role as well. | 11/14/2022 |
| 5723 | Bardy Diagnostics Skaneateles Falls, NY Electrical Engineer I Bachelor of Science degree in engineering. Exp: 1+ years |
You are a problem solver. Complex projects or unexpected challenges are just opportunities to bring your considerable abilities to use. Whether working independently or with a trusted team, you are always ready to tackle a project and work hard to find solutions. The Electrical Engineer, Sustaining will be responsible for the design, design verification, and design documentation for our Front Line Care business unit. | 11/14/2022 |
| 5724 | BASi Research Products Rockville, MD Associate Scientist I (In Vitro Cytogenetics) Bachelor’s degree in a scientific discipline (i.e., Biology, Chemistry, Biochemistry, etc.) Exp: 1+ years |
Position Responsibilities: Perform a wide variety of in vitro assays or tests required to characterize product or material safety Maintain sterile and good cell/tissue culture techniques Prepare study reagents in accordance with SOPs and study instructions Use and maintain scientific equipment, instrumentation and computer systems Conduct pre-designed assays using basic laboratory techniques and skills Make scientific observations, maintain detailed data books/documentation and ensure all documentation fulfills generally accepted professional/industry standards and GLP regulations | 11/14/2022 |
| 5725 | BASi Research Products Raleigh, NC Research Associate I B.S. degree Exp: > 0-1 year |
Join us in embracing research and science to impact the health and well-being of people all over the world. Inotiv is expanding our In Vivo Toxicology team. We are a contract research organization performing regulated toxicology studies in laboratory rodents for commercial and governmental clients. J | 11/14/2022 |
| 5726 | BASi Research Products Rockville, MD Associate Scientist II (Secondary Assays) Master’s degree in a scientific discipline (i.e., Biology, Chemistry, Biochemistry, etc.) Exp: 0+ years |
Position Responsibilities: Perform a wide variety of in vitro or in vivo Comet assays or tests required to characterize a product or material safety Maintain sterile and good cell/tissue culture techniques Prepare study reagents in accordance with SOPs and study instructions Use and maintain scientific equipment, instrumentation and computer Conduct pre-designed or custom assays using laboratory techniques and skills Perform in vivo Comet tasks such as: necropsy, tissue collection, tissue processing slide preparation and electrophoresis Make scientific observations, maintain detailed data books/documentation, and ensure all documentation fulfills generally accepted professional/industry standards and GLP regulations Analyze data and interpret results with input from senior staff, as needed Ensure all testing guidelines are followed for assays performed | 11/14/2022 |
| 5727 | BASi Research Products West Lafayette, IN Bio Analyst I B.S. in chemistry or biology Exp: one year |
Position Summary Conducts sample analysis with data interpretation and basic troubleshooting. Conducts method development and method validation experiments. Assists with general housekeeping and assist other departmental personnel as necessary. | 11/14/2022 |
| 5728 | BASi Research Products Raleigh, NC Research Assistant A.S. or B.S. in biology or related field Exp: 0-3 years |
The Genetic Toxicology Group conducts standard and custom genetic toxicology testing and applied research supporting preclinical studies for both federal and commercial clients. | 11/14/2022 |
| 5729 | Bausch & Lomb Wilmington, MA Quality Engineer I Bachelor of Science, preferably in Engineering, Science (Chemistry, Biology, Physics, etc) or Math (Statistics). Exp: 1-2 years |
Responsible for providing quality engineering and quality management systems support to the Wilmington manufacturing site. | 11/14/2022 |
| 5730 | Bausch & Lomb Rochester, NY Scientist I - Formulations B.S. in chemistry or related biological science discipline will be considered. Exp: 0 to 4 years |
Scientist I position supporting the research, design, and development of lens care products to drive future technologies. A laboratory based position within the R&D Formulation team at the Rochester, NY site. This position will focus on the preparation and characterization of new solution prototypes and marketed product support. | 11/14/2022 |
| 5731 | Bausch Health Bothell, WA Quality Assurance Specialist I (WA) Quality Assurance Specialist I (WA) Quality Assurance Specialist I (WA) 4 years bachelor level degree in Science, engineering or other similar discipline. Exp: 1-3 years |
The Quality Assurance Specialist I will perform complaint investigation activities for product complaints and Adverse Events with cross functional team members and provide complaint investigation reports in compliance with Solta procedures, Food and Drug Administration (FDA), International Standards Organization (ISO), Quality System requirements, and other regulatory guidelines. | 11/14/2022 |
| 5732 | Beckton Dickinson Glens Falls, NY Manufacturing Quality Engineer (onsite) Bachelor’s Degree in Engineering or Technical Sciences. Exp: 1 years |
The Quality Engineer will be responsible for engineering support and direction of QC/QA activities to support design to manufacturing and manufacturing to manufacturing transfers at the GFO site. | 11/14/2022 |
| 5733 | Be Biopharma Kendall Square, MA Process Engineer, B Cell Core BS or MS in Chemical Engineering, Biology, Analytical Chemistry, Biochemistry, Cell & Molecular Biology, or related discipline Exp: 0-2 years |
Be Biopharma is seeking a candidate to help build the B Cell Core Team. Team members will work on early-stage process development and production of novel autologous and allogeneic B cells. There are three major responsibilities within B Cell core- optimize methods for B cell manufacture; deliver B cells for in vivo and developmental studies; and lead documentation for internal and external tech transfer. Roles and responsibilities will be given based on experience and knowledge in the cell therapy field. This is an excellent opportunity for career growth as you would interact with various programs teams and would be involved in regulatory document preparation. | 11/14/2022 |
| 5734 | Be Biopharma Kendall Square, MA Sr./Research Associate, Analytical Development BS or MS in Chemical Engineering, Biology, Analytical Chemistry, Biochemistry, Cell & Molecular Biology, or related discipline Exp: 0-2 years |
Role: Be Biopharma is seeking a Sr. / Research Associate candidate to join the growing Analytical Development (AD) department. AD is responsible for establishing molecular, cell-based, and impurities methods used to characterize B cell drug products as well starting materials (ie AAV vector). The Sr. / Research Associate will be tasked with leading / supporting the different stages of assay development, feasibility, robustness, and prequalification. This is an excellent opportunity for career growth as you would interact with various programs teams and be involved in regulatory document preparation. | 11/15/2022 |
| 5735 | Be Biopharma Kendall Square, MA Sr. Research Associate/Associate Scientist, Cell Engineering BS/MS in Cell and Molecular Biology, Bioengineering, Immunology, Pharmacology or a related field Exp: 1+ years |
Be Biopharma is looking to hire a Senior Research Associate / Associate Scientist to join our Cell Engineering Team and support the genomic safety assessment for our B cell medicines. We are looking for highly motivated, experienced, and innovative thinkers to join our growing team of passionate researchers to leverage B cells as a novel class of cellular medicine. This is an exciting opportunity to be part of a foundational team and help build Be Bio! | 11/15/2022 |
| 5736 | Berkeley Lights Emeryville, CA Electrical Engineer BSEE/MSEE degree or equivalent Exp: 0-3 years |
Berkeley Lights is looking for a dynamic and energetic person to fill the role of Electrical Development Engineer. As a member of our Hardware Engineering team, you will be responsible for contributing to the hardware development of our commercial product offerings. This person must be able to work with a talented team to engineer robust solutions to our toughest problems. This person must be passionate about engineering, a quick learner, and love working at a dynamic startup company that will change the world! | 11/15/2022 |
| 5737 | BGI San Jose, CA LC/MS Research Associate – Small Molecule B.S. degree with biochemistry/chemistry major or related field Exp: 0-2 years |
San Jose Mass Spec Lab of BGI Americas is seeking an exceptional and motivated research associate with competitive compensation. The main responsibility of this position includes, but not limited, to support the SJMS production team 1) to turn around routine customer and research projects, 2) to maintenance and operate LC-MS instrument, 3) to assist lab manager to build up metabolomics and lipidomics capability in SJMS lab, 4) to support other departments when needed. A candidate with metabolomics/lipidomics LC-MS experience is a plus; a candidate with small molecule sample prep experience is a plus. An ideal candidate will need to demonstrate that they are capable of consistently following Standard Operational Procedures (SOPs) to consistently perform sample preparation procedures for metabolomic or lipidomics analysis. A candidate with hands-on experience in HPLC, Orbitrap mass spec and working with biofluids is a plus. | 11/15/2022 |
| 5738 | BGI San Jose, CA LC/MS Research Associate – Proteomics B.S. degree with biochemistry/chemistry major or related field Exp: 0-2 years |
BGI Americas San Jose Mass Spec (SJMS) center is seeking an exceptional and motivated research associate to join our Proteomics department at our San Jose facility. The main responsibility of this position includes, but not limited, to support the SJMS production team 1) to turn around routine customer and research projects, 2) to maintenance and operate LC-MS instrument, 3) to assist lab manager to build up additional proteomics capability in SJMS lab, 4) to support other departments when needed. An ideal candidate will need to demonstrate that they are capable of consistently following Standard Operational Procedures (SOPs) to consistently perform sample preparation procedures for proteomics and biologics characterization analysis. A candidate with hands-on experience in HPLC, Orbitrap mass spec and, working with biofluids is a plus. | 11/15/2022 |
| 5739 | BigHat Biosciences San Mateo, CA Research Associate (Production) BS in Biology or Chemistry Exp: 1+ year(s) |
BigHat Biosciences is seeking a self-motivated individual for a Research Associate, Production role to execute key experiments and optimize protocols to fuel BigHat’s high-throughput, automated platform for producing and characterizing antibodies. | 11/15/2022 |
| 5740 | BioAssay Systems Hayward, CA Research Associate - Assay Development A bachelors degree in biochemistry, chemistry, biology, or related field Exp: 1-2 years |
We currently have an exciting opportunity for an enthusiastic research associate to join our growing R&D team. This position will play an important role in increasing our already extensive catalog of biochemical colorimetric, fluorescent, and luminescent 96-well and 384-well plate assay kits. In addition, this role will assist our analytical services department in establishing additional techniques to expand our service capabilities. This candidate may also be involved in providing technical support to customers. This is a fantastic opportunity for a motivated recent graduate to be part of a successful and expanding team while learning a number of laboratory skills in a supportive environment. In addition, working on service projects will expose the candidate to multiple other companies and research areas. Moreover, as a small company we offer ample opportunities for professional growth and faster than average promotions. | 11/15/2022 |
| 5741 | BioAssay Systems Hayward, CA Research Associate - Manufacturing college degree in chemistry, biochemistry or biology Exp: 1-2 years |
We are currently looking for an enthusiastic research associate to join our manufacturing team. This position will entail preparing reagents for our assay kits, QCing, and packaging the finished products. This candidate may also join part time in our R&D team. | 11/15/2022 |
| 5742 | BioFire Diagnostics Salt Lake City, UT Research Associate I/II B.S. in molecular biology, biology, biomedical sciences, or a related field is desired Exp: 0-2 years |
The Molecular Systems Research Associate I or II (RA I/II) position is a full-time, non-exempt position. This position is part of a team working on various laboratory procedures involving nucleic acid isolation methods and PCR under general guidance. This person will work closely with other research associates or scientists in the research lab. | 11/16/2022 |
| 5743 | BioFire Diagnostics Salt Lake City, UT Research Associate I/II Bachelor’s degree with emphasis in science. Exp: RAI: 0-2 years |
The Research Associate I/II is a technical hourly position with laboratory responsibilities. The RA II works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of FDA and other regulatory submissions. Tasks will focus on molecular and microbiological experiments and procedures (e.g. nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to effectively and respectfully communicate and coordinate with peers and supervisor(s). | 11/16/2022 |
| 5744 | BioFire Diagnostics Salt Lake City, UT Research Associate I bachelor’s degree with an emphasis in science is preferred. Exp: entry-level |
The Research Associate I is a technical, hourly position with laboratory responsibilities. The RA I works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g. nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to effectively and respectfully communicate and coordinate with peers and supervisor(s). | 11/16/2022 |
| 5745 | BioFire Diagnostics Salt Lake City, UT Research Associate I Bachelor’s degree in a scientific discipline Exp: 0-2 years |
This is a full-time non-exempt position. This position is part of a team working on a variety of laboratory procedures involving real-time PCR using established methods and techniques under general guidance. This person works closely with other research associates in the department. Performs general lab duties, designs and conducts experiments, collects and analyzes data, and keeps an accurate record of all work done in accordance with the quality system. Requires some problem-solving skills. Normally receives general instructions on routine work and detailed instructions on new assignments. Reports to the Senior Research Associate or Scientist. | 11/16/2022 |
| 5746 | BioFire Diagnostics Salt Lake City, UT Research Associate I/II B.S. in biology, biomedical sciences, chemistry, or a related field Exp: 0-2 years |
The Molecular Systems Research Associate I or II (RA I/II) position is a full-time, non-exempt position. This position is part of a team working on various laboratory procedures involving nucleic acid isolation methods and PCR under general guidance. This person will work closely with other research associates or scientists in the research lab. | 11/16/2022 |
| 5747 | BioFire Diagnostics Salt Lake City, UT Research Associate I/II Bachelor’s degree in a scientific discipline Exp: 0-2 years’ |
This is a full time non-exempt position. This position is part of a team working on a variety of laboratory procedures involving real-time PCR using established methods and techniques under general guidance. This person works closely with research associates in the research lab. Performs general lab duties, designs and conducts experiments, collects and analyzes data and keeps an accurate record of all work done in accordance with the quality system. Requires some problem solving skills. Normally receives general instructions on routine work, detailed instruction on new assignments. Reports to a senior research associate (RA IV or above) or a Scientist. | 11/16/2022 |
| 5748 | BioLegend San Diego, CA Research Associate I - Immunoassay BS in a Biology, Chemistry or other related field Exp: 1 year |
This position is responsible for supporting immunoassay products development and manufacturing in the Biomarker Immunoassay group. The Research Associate will be involved in all aspects of the product development processes including designing, initiating, testing, troubleshooting, testing materials manufacturing, technical instruction transferring, and product launching. More specifically, he or she will be working with an experienced scientist on testing new hybridoma clones, qualifying the raw materials used for immunoassay products manufacturing and new immunoassay product development and launching. These immunoassay products may allow simultaneously detection of up to 13 important biomarkers for inflammatory diseases, stem cells, cancer, cardiovascular disease or neuron degenerative diseases, and will be very useful tools for the biomedical research community. This position is a great opportunity for gaining working experiences in growing business in a fast-pace biotech industrial environment. He or she will be able to manage the assigned function and tasks with great communication skills in a timely manner with independence after appropriate training. | 11/16/2022 |
| 5749 | bioMerieux Durham, NC Analytical Chemist (LC-MS/MS) Degree in Chemistry or applicable Life Sciences with B.S Exp: 1-3 years |
Participate and assist in planning and conducting activities to develop new products or methods/techniques within BioMerieux Clinical Microbiology product portfolio in full compliance with current quality and safety standards Provide technical assistance for activities to improve or support existing products, methods or techniques | 11/16/2022 |
| 5750 | BioReliance St Louis, MO cGMP Associate Production Scientist Bachelor’s Degree in Chemistry, Biochemistry, Chemical Engineering, or other life science discipline Exp: 1+ year |
The Associate Production Scientist at MilliporeSigma is responsible for the manufacturing of active biopharmaceutical ingredients (APIs) Chemicals and bulk pharmaceuticals regulated by the Food and Drug Administration (FDA). The Associate Scientist is responsible for following manufacturing protocols, consistent with and established according to current Good Manufacturing Practices (cGMP) and ensuring the accuracy of documentation. | 11/16/2022 |
| 5751 | BioReliance St Louis, MO cGMP Associate Production Scientist Bachelor’s Degree in Chemistry, Biochemistry, Chemical Engineering, or other life science discipline Exp: 1+ year |
The Associate Production Scientist at MilliporeSigma is responsible for the manufacturing of active biopharmaceutical ingredients (APIs) Chemicals and bulk pharmaceuticals regulated by the Food and Drug Administration (FDA). The Associate Scientist is responsible for following manufacturing protocols, consistent with and established according to current Good Manufacturing Practices (cGMP) and ensuring the accuracy of documentation. | 11/17/2022 |
| 5752 | BioReliance Branchburg, NJ Process Excellence Engineer Bachelor’s Degree or Master’s Degree in Chemistry, Chemical Engineering, Materials Science, or other scientific or technical discipline Exp: 1+ years |
We are seeking an engineer who is capable of effectively leveraging their knowledge and experience in product development and quality systems to deliver products (photoresists, coatings, ancillaries) to customers in the semiconductor industry. | 11/17/2022 |
| 5753 | BioReliance Rocklin, CA Histology Lab Manufacturing Technician Bachelors’ Degree in Chemistry, Biology, or other Biological Science discipline Exp: 1+ years’ |
At MilliporeSigma, the Histology Lab Manufacturing Technician is responsible for performing Histology related functions. This includes microtomy, staining of tissue by immunohistochemistry (IHC), tissue processing and embedding. The ideal candidate has experience using a microtome and is eager to work as a team to meet departmental goals and deadlines. This position reports to the Manufacturing Supervisor as part of the Operations team located at the Rocklin Site, where we manufacture products for use in in vitro diagnostic (IVD) IHC. | 11/17/2022 |
| 5754 | BioReliance Miamisburg, OH Associate Production Scientist Bachelor’s Degree in Chemistry, Biochemistry, or other Science discipline Exp: <1 year |
As an Associate Production Scientist in Miamisburg, OH, you will manufacture or evaluate products according to established protocols, provide technical support to others, and perform operations in support of the group and department. | 11/17/2022 |
| 5755 | BioReliance Sheboygan Falls, WI Associate Quality Control Chemist (Laboratory) Bachelor’s Degree in Chemistry, Biochemistry,?Chemical Engineering, or other Life Science discipline Exp: <1 year |
The Associate Quality Control Chemist (Lab) will evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. | 11/17/2022 |
| 5756 | LGC Biosearch Technologies Cumberland, ME Manufacturing Chemist I (47324) Bachelors degree in life science field or other related science or medical curriculum Exp: no formal experience |
The Manufacturing Chemist I fulfils the essential role of preparing reagents, buffers, stocks, and other solutions using established procedures within the operations laboratory. They will use general laboratory equipment and techniques to perform these tasks under both direct and indirect supervision. They are expected to perform routine analysis and interpretation of test results against established acceptance criteria with limited judgment. | 11/17/2022 |
| 5757 | LGC Biosearch Technologies Petaluma, CA Therapeutic Production Technician I - Entry Level- Day Shift (47172) Bachelors degree preferred with a Science background Exp: 1 or more years’ |
The Therapeutic Production Technician will support oligonucleotide manufacturing processes in the LGC Biosearch Technologies’ Petaluma Therapeutic GMP suite. Activities include: daily calibration of instruments, stocking materials, cleaning and maintaining labware. | 11/17/2022 |
| 5758 | LGC Biosearch Technologies Petaluma, CA Quality Control Analyst - Chem Lab (47184) Bachelor’s degree in relevant field such as chemistry, biochemistry, chemical engineering, pharmaceutical sciences Exp: 1 years |
The Quality Control Analyst focus on the performance of analytical testing activities within the QC Chemistry lab. They are responsible for testing intermediate and finished chemical products, analysing the results of Quality Control testing, and comparing results to established specification and customer requirements. In addition, they perform testing and/or review of incoming goods. This position reports to the Quality Control Supervisor/Quality Control Manager. | 11/17/2022 |
| 5759 | LGC Biosearch Technologies Manchester, NH Assistant Chemist 1 (47120) Bachelor of Science degree, chemistry is preferred Exp: 0-2 years |
Prepare aqueous and/or metallo-organic stock and custom samples per QSPs Follows standard operating procedures Operates basic laboratory equipment including lab balances and analytical instrumentation as trained Follows, as well as possesses, strong written and verbal instructions Follows complex procedures and operations Demonstrates consistent, reliable performance Works effectively as part of a team as well as independently with minimal supervision Exhibits organizational skills and attention to detail Demonstrates math and computer skills Meets production goals Learn quickly and is easily trainable Maintains the ability to problem solve and apply retained knowledge Exemplify the LGC core values on a day-to-day basis Perform other duties as assigned Ability to learn chemical nomenclature, properties and proper handling of chemicals | 11/17/2022 |
| 5760 | Bio-techne Minneapolis, MN Advanced Research Associate Master’s degree in a related field Exp: up to 2 years |
This position is responsible for participating in the development of Bio-Techne's various product lines. You will maintain knowledge of multiple products and procedures as well as draft and revise standard operating procedures in order to further the ongoing development of new and existing products to help advance Bio-Techne's evolving portfolio. | 11/17/2022 |
| 5761 | Aldevron Danvers, MA Research Associate IHC BSc or BA in a Scientific discipline Exp: 1 to 4 Years |
Research Associates are responsible for the undertaking of research and development activities to support contracted pharma projects to develop companion diagnostics IVDs. The Research Associate will be responsible for performing required laboratory studies, including making observations, reporting data and providing results to support key decisions within the Pharma Partnerships business unit. A shown ability to communicate (verbal and written) and work with all levels of staff is fundamental to this role. Ensure all work is conducted in accordance with applicable protocols and work instructions and that all work is appropriately documented per procedure | 11/7/2022 |
| 5762 | Aldevron Coralville/ Des Moines, IA Research Scientist II - Verification and Validation Master’s degree (in Biology, Genetics, Chemistry or a related life sciences field) Exp: one or more years |
Purpose Statement: The Research Scientist II, under minimal supervision, conducts bench scientific experimentation that advances the basic science of nucleic acids and nucleic acid biochemistry and assists with the development and characterization of new IDT genomics products in NGS, qPCR and functional genomics. This position is responsible for planning and executing experiments, analyzing data and reporting/presenting findings as well as supporting IDT customers. This individual will aid in the development and characterization of new genomics products in NGS and qPCR to help create cutting edge, robust new products, and assays for basic research, agricultural, and clinical applications. The preferred candidate will have previous bench level experience in a research or industry setting and strong knowledge in basic laboratory and molecular biology techniques. Background in next-generation sequencing and/or qPCR are a plus. | 11/7/2022 |
| 5763 | Aldevron Sunnyvale, CA Scientist II Master’s degree in Molecular biology/Bioinformatics or related field Exp: 1+ years |
The Scientist II is responsible for planning, executing, and discussing experiments that drive product development. As a Scientist II, the employee has opportunities to learn Cepheid integrated platforms and technology with the goal of developing infectious disease tests to meet existing and emerging customer needs. This position is part of Cepheid’s Infectious Disease R&D and will be located in Sunnyvale, CA. The Infectious Disease R&D Business Unit is comprised of research and development scientists driving New Production Introduction (NPI) that aligns with Cepheid’s strategic plan to fortify our leadership position in the Molecular Diagnostic market. | 11/7/2022 |
| 5764 | AllCells Huntsville, AL Laboratory Technician I - CP Bachelor of Science degree in biology (or related field) or 2 yr MLT degree with ASCP certification Exp: 1-3 years |
Position Summary: The Laboratory Technician I- Cell Processing, contributes to our mission by processing biospecimen samples for cryopreservation or further characterization based on standard operating procedures. Hours are approximately 9am-6pm, but can fluctuate based on business needs. Includes a Saturday rotation. | 11/7/2022 |
| 5765 | AllCells Huntsville, AL QC Specialist I - Cell & Gene Therapy Bachelors of Science in Biology, Microbiology, or other life sciences related field Exp: 0-2 years’ |
The Quality Control Specialist I is responsible for testing, inspection and release of materials and finished products, will execute routine in-process and final product analysis, in accordance with specific procedures and specifications. | 11/7/2022 |
| 5766 | AllCells Huntsville, AL Laboratory Technician I - CGT Bachelor of Science degree in biology or related field or 2 year MLT degree with ASCP certification Exp: 1-3 years |
Position Summary: The Laboratory Technician I- Cell and Gene Therapy, contributes to our mission by processing blood samples collected through leukapheresis for cryopreservation or further characterization based on standard operating procedures. Hours are approximately 10am-7pm, but can fluctuate based on business needs. | 11/7/2022 |
| 5767 | AllCells Newtown, PA Histology Technologist Master's degree in a laboratory science (i.e. biology, chemistry, or other lab science) Exp: |
The Histology Technologist contributes to our mission by supporting the Study Director throughout the duration of a project including sponsor and study director updates, developing study design, assisting with proposal writing, and presenting to clients. | 11/7/2022 |
| 5768 | Allogene Therapeutics South San Francisco, CA Associate Scientist, In Vivo Pharmacology Master of Science degree Exp: 1+ years |
We are seeking a hard-working, enthusiastic Associate Scientist/Senior Associate Scientist to contribute to developing next-generation AlloCAR T cells for the treatment of hematologic malignancies and solid tumors. You will be working closely with researchers to support preclinical in vivo studies utilizing tumor xenograft models. The successful candidate will have extensive experience working with mice and will have the opportunity to learn new in vitro skills, developing experience in flow cytometry for CAR T cell pharmacokinetics. The ideal candidate will show the ability to conduct in vivo studies with minimum supervision and to generate high-quality data to support Allogene’s pipeline. | 11/7/2022 |
| 5769 | Allogene Therapeutics South San Francisco, CA Associate Scientist/Scientist, Protein Science/Antibody Engineer BS. or MS. degree in life science or related field required (or relevant experience) Exp: 1+ years |
Allogene Therapeutics is seeking a highly motivated Associate Scientist/ Scientist in the Protein Science group to support the antibody/protein engineering, production, conjugation, and characterization needs across all our research and development programs. The position will report to the Sr Principal Scientist, Protein Engineering and be responsible for continuing our development and implementation of these core capabilities in support of our pipeline of allogeneic CAR T cells. The ideal candidate is an individual who is interested in working in a fast-paced, dynamic, and highly collaborative biotech environment with a willingness and ability to successfully take on new challenges. | 11/7/2022 |
| 5770 | Alnylam Pharmaceuticals Cambridge, MA Associate Scientist II, Translational Research B.S/M.S. degree in a biological discipline such as Molecular Biology, Cell Biology or Biochemistry Exp: 0-3 years |
We are seeking a talented and enthusiastic candidate to fill an Associate Scientist II position within Alnylam’s Discovery and Translational Research team based in Kendall Square, Cambridge MA. This position is an opportunity to potentially see one’s work progress from the bench to the clinic and positively impact patients’ lives. This position involves performing exploratory work and preclinical target validation as part of a multidisciplinary team involved in the discovery of RNAi compounds for a variety of novel indications and support their entry into the clinic. The successful candidate will have a passion for science, attention to detail and desire to learn about new disease areas and lab techniques. Experience or willingness to learn in vivo rodent techniques is required. | 11/7/2022 |
| 5771 | Alpine Immune Services Seattle, WA Research Associate/Senior Research Associate, Biomarkers Bachelors or Masters Exp: 1+ years |
Alpine Immune Sciences is seeking an enthusiastic and highly motivated Research Associate|Senior Research Associate to join the Clinical Biomarker group. This individual will be primarily responsible for supporting flow cytometry and other biomarker analysis of clinical samples to support our protein-based immunotherapeutics platform. The successful candidate must have hands-on experience with design and analysis of multicolor flow cytometry panels. Excellent written and oral communication skills, effective team contribution, and strong organizational skills are essential. | 11/7/2022 |
| 5772 | Alstem Richmond, CA Research Associate B.S. or M.S. degree in Biochemistry, Molecular Biology or related discipline. Exp: 1 year |
ALSTEM is looking for a highly organized and energetic Research Associate with a B.S or M.S. degree to join its scientific team. The candidate will be responsible to work as a team at all levels which will include but will not be limited to product testing and QC, and custom service projects following SOPs and protocols to support customer workflows. | 11/7/2022 |
| 5773 | Amarex Clinical Research Ypsilanti, MI Technician II - Engineering Lab Technician Bachelor or Associate degree in an Engineering or Scientific discipline Exp: One year |
As a Technician II for the Engineering/Plastics Lab, you will be responsible for conducting basic testing on plastics, pipes, fittings and other related plumbing products to specific standards and procedures. | 11/7/2022 |
| 5774 | AmbioPharm North Augusta, SC QC Chemist III Masters Degree in Chemistry or life sciences Exp: 1-2 years |
Use basic understanding and knowledge of techniques, instrumentation and lab functions to identify problems and support the completion of work assignments. Hands on experience with HPLC/UPLC, GC, GC-MS, IC, KF and other routine analytical equipment such as pH meter and balance. Perform quality control routine critical testing for raw material/ Intermediate/ Release / Stability testing and evaluate stability trends. Ensure completion of all the testing release , stability and validation work in timely manner. Perform Method development and method validation execution, including writing protocols and reports. Must be proficient. Responsible for reviewing analytical laboratory raw data and electronic records. Assist the QC group with writing and editing of deviations, CAPA, OOS and OOT. Maintain the QC lab by ordering supplies routinely used for testing. Assist the QC/QA group with writing and editing of SOPs and STPs. Assist in equipment qualification and troubleshooting Train and assist junior chemist to ensure completion of testing Other duties as assigned | 11/7/2022 |
| 5775 | AmbioPharm North Augusta, SC QC Chemist I Bachelor’s Degree in Chemistry or life sciences Exp: 1-2 years |
Use basic understanding and knowledge of techniques, instrumentation and lab functions to identify problems and support the completion of work assignments. Perform and review QC release testing. Support routine analytical testing using GC, KF, and HPLC. Assist the QC/QA group with writing and editing of SOPs and STPs Support analytical method development. Perform method transfer and validation activities. Perform OQ/PQ for the Quality Control Equipment. Other duties as assigned | 11/7/2022 |
| 5776 | AmbioPharm North Augusta, SC QC Chemist II Master’s Degree in Chemistry or life sciences Exp: 1-2 years |
Use basic understanding and knowledge of techniques, instrumentation and lab functions to identify problems and support the completion of work assignments. Perform and review QC release testing. Support routine analytical testing using GC, KF, and HPLC. Assist the QC/QA group with writing and editing of SOPs and STPs Support analytical method development. Perform method transfer and validation activities. Perform OQ/PQ for the Quality Control Equipment. Other duties as assigned. | 11/8/2022 |
| 5777 | AmbioPharm North Augusta, SC QA Analytical Associate II Bachelors Science Degree is required. (Chemistry, Biology, or other Life Science degree) Exp: 0+ years |
Quality Assurance review and approval of analytical data for release of CGMP manufacturing batches (UPLC, HPLC, IC, etc) Review of instrument audit trails for compliance Quality Assurance review and approval of analytical method protocols, validations and reports (UPLC, HPLC, IC, etc) Creation of CoAs for analytical testing Review and approval of analytical change controls and deviations and CAPAs Perform internal facility and quality system audits. Assist with SOP revisions and writing new SOPs. Other duties as requested by the Quality Management. | 11/8/2022 |
| 5778 | AmbioPharm North Augusta, SC Microbiologist BS in Microbiology or life sciences. Exp: 1-5 years |
Perform procurement and testing of: city and pharmaceutical grade water per USP guidelines and SOP; product for bioburden, endotoxin per USP guidelines and SOP; stability samples per SOP; environmental monitoring sample (viable and non-viable) per USP guidelines and SOP, as scheduled (daily, weekly, monthly, quarterly) Support production in qualification of clean rooms and water systems. Data entry for trending reports Perform QC testing and release of microbiological media, reagents, and stock cultures Maintenance of stock cultures Use of aseptic technique for sampling and testing of all samples collected for microbiological analysis Documentation of all activities per current good documentation practices as described in SOP Use basic understanding of and knowledge of techniques, instrumentation and lab functions to identify problems, initiate investigations and support completion of work assignments | 11/8/2022 |
| 5779 | AmbioPharm North Augusta, SC Research & Development Chemist I BS/BA in chemistry or related field Exp: 1 year |
Assist in performing peptide synthesis using commercial peptide synthesizers. Monitor upstream process progress via HPLC, UPLC, LC/MS, and other qualitative methods. Support routine analytical testing and analytical method development activities using HPLC/UPLC. Assist in preparative scale chromatography for peptide purification development or non-GMP activities. Responsible for recording and reporting Research and Development results in a suitable proposal format as deemed appropriate in support of new and existing products. Assist with the coordination and execution of equipment qualification activities in accordance with regulatory requirements. As needed, work in a GMP environment to assist in the transfer of peptide manufacturing process and analytical development strategies. As needed, follow approved instructions such as Batch Records, Standard Operation Procedures, Standard Test Procedures, etc. operate and maintain equipment for Research and Development, manufacturing and in-process testing as needed. | 11/8/2022 |
| 5780 | Ambys Medicines South San Francisco, CA Research Associate / Senior Research Associate, Pharmacology Bachelor’s degree Exp: 1+ years |
We are seeking a collaborative and detail-oriented Research Associate to join our Pharmacology group. You will contribute as part of a multidisciplinary team to develop novel therapies to treat liver diseases using cell therapy strategies. In this position, you will report to our In Vivo Manager and will work in a team environment performing a variety of tasks and experiments in support of our in vivo pharmacology studies. | 11/8/2022 |
| 5781 | Ambys Medicines South San Francisco, CA Associate/Senior Associate, Quality Control, Cell Therapy BS or MS degree in a biological science discipline Exp: 1-5 years |
Our Technical Operations team is growing, and we have an exciting opportunity for a talented and motivated Quality Control Associate I/II to support our cell and gene therapy manufacturing activities. You will contribute as part of a multidisciplinary team to develop novel cell therapies to treat liver diseases using cell and gene therapy strategies. In this position, you will be critical to the overall strategy and growth of the CMC organization at Ambys as we build out a new cGMP facility. You will report to our Manager, Quality Control Method Transfer, and Validation. You will be responsible for helping develop and execute cGMP-compliant testing of manufactured hepatocytes for supporting process development, IND-enabling studies, and clinical studies. | 11/8/2022 |
| 5782 | Ambys Medicines South San Francisco, CA Microbiology Analyst, Quality Control Bachelor’s degree in microbiology, biology, or chemistry. Exp: 0-3 years |
Our Technical Operations team is growing, and we have an exciting opportunity for a talented and motivated Microbiology Analyst for Quality Control to support our cell therapy manufacturing activities. You will contribute as part of a multidisciplinary team to develop novel cell therapies to treat liver diseases using cell therapy strategies. In this role, you will provide support to Quality Control Department projects as needed activities for the new cGMP facility. | 11/8/2022 |
| 5783 | AnaSpec Fremont, CA Research Associate-Assay Kits BS in Biochemistry, Chemistry, Cell Biology or related discipline Exp: 0-3 years |
Perform assay kit production and QC tests: enzyme activity assays, protein labelling and conjugation, protein expression/purification Manage routine activities, including meticulous record keeping Order laboratory supplies and reagents, maintain inventory Participation in R&D projects expected Ensure implementation, compliance, and continuous improvement of QMS through SOP documentation. | 11/8/2022 |
| 5784 | AnaSpec Fremont, CA Research Associate-Antibodies BS in Biochemistry, Chemistry, Cell Biology or related discipline Exp: 0-3 years |
Perform antibody purification and characterization, protein expression/purification; protein/peptide labeling and conjugation Manage routine activities, including meticulous record keeping Order laboratory supplies and reagents, maintain inventory Participation in R&D projects expected Ensure implementation, compliance, and continuous improvement of QMS through SOP documentation Other duties as assigned by Management | 11/8/2022 |
| 5785 | AnaSpec Fremont, CA Synthesis Chemist I BS or above in Chemistry, Organic Chemistry, or related disciplines Exp: 1-3 years |
The Synthesis Chemist I will perform peptide production and conduct in-process testing using Good Laboratory Practices (GLP). As a member of the Synthesis department, the Synthesis Chemist I will work closely with the Purification, QC, and Sales & Business Development departments. | 11/8/2022 |
| 5786 | ANI Pharmaceuticals Baudette, MN QC Chemist/Sr. QC Chemist Bachelors degree in chemistry, biochemistry, microbiology or closely related field/major. Exp: QC Chemist – 1-3 years |
The QC Chemist position is responsible for independently performing testing in a pharmaceutical Quality Control laboratory. All work will be conducted in accordance with standard operating procedures and test methods. This includes performing testing on raw material, in-process and finished product samples. Execute compendia method validations, method transfers and validation support of new product development. Set up and confirm suitable operation of equipment and instrumentation. Collect data and generate/report results in accordance with governing test methods and SOPs. | 11/8/2022 |
| 5787 | Ansh Labs Webster, TX Scientist (R&D) Master’s degree in Biological/Chemical Sciences/Biotechnology or related area Exp: 1 year |
As a key member of the R&D Department, this individual will provide critical scientific skills to assist in the development and scale-up of immunodiagnostic products on various platforms (microtiter based ELISA, magnetic particle based immunoassays, Lateral Flow assays and micro fludics based immunoassays). | 11/8/2022 |
| 5788 | Aquinnah Pharmaceuticals Cambridge, MA RESEARCH ASSOCIATE Master’s degree in neuroscience, cell biology or related discipline Exp: 1+ years |
This position is laboratory-based and requires strong experimental skills with a background in cell biology, molecular biology, or biochemistry. Under supervision, the candidate will assist in duties including, but not limited to: cell culture maintenance, compound screening, biochemical assays, immunocytochemistry, and analysis using state of the art high-content imaging. Strong communication skills are required including the ability to analyze and report on the results. The candidate will be expected to function efficiently and cooperatively within a team and maintain accurate and clear project records. The ideal candidate will be creative, energetic and motivated. Candidates should have a Bachelor’s or Master’s degree in neuroscience, biology, or related field. Salary will be competitive and commensurate with experience. | 11/9/2022 |
| 5789 | Arraystar Rockville, MD Lab Assistant - Molecular Biology Bachelor’s degree in a relevant biological field. Exp: 1-2 years’ |
Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. Assist with the generation and updating of laboratory SOPs. Perform basic lab maintenance tasks such as ordering lab supplies, and keeping detailed lab records. Communicate with clients to obtain/verify information of their projects, orders or requests. | 11/9/2022 |
| 5790 | ArunA Biomedical Athens, GA Process Development Associate II MS degree in relevant field Exp: 0-2 years' |
• Set up and execute experiments related to process development • Set up and execute experiments associated with scale-up production processes • Troubleshoot experiment errors and assist in root-cause analyses to determine the source of error • Perform data analysis, identify trends, and incorporate findings into development and control strategies. • Manage multiple projects simultaneously with minimal supervision • Troubleshoot software or equipment malfunction to determine the source of error. • Ability to use a variety of equipment such as pipettors, balances, laminar flow hoods, incubators, autoclaves, microscopes, centrifuges, plate readers, and particle analyzer. • Maintain detailed records that are legible, accurate and readily understood. • Complete documentation needed to support development procedures including data capture forms, equipment logbooks, or inventory forms. • Compile laboratory test data and perform appropriate analyses. | 11/9/2022 |
| 5791 | ArunA Biomedical Athens, GA Analytical Development and Quality Control Associate II MS degree in relevant field Exp: 0-2 years' |
• Conduct routine analyses of in-process materials, drug substance, drug product and stability samples following written procedures. • Expand skill set of analytical technologies and test methods and assist in the development of test methods. • Participate as an analyst in qualification/validation of various biological and chemical QC assays. • Ability to perform aseptic technique and mammalian cell culture. • Perform data analysis, identify trends, and incorporate findings into development and control strategies. • Manage multiple projects simultaneously with minimal supervision • Troubleshoot software or equipment malfunction to determine the source of error. • Ability to use a variety of equipment such as pipettors, balances, laminar flow hoods, incubators, autoclaves, microscopes, centrifuges, plate readers, and particle analyzer. • Maintain detailed records that are legible, accurate and readily understood. • Complete documentation needed to support testing procedures including data capture forms, equipment logbooks, or inventory forms. • Compile laboratory test data and perform appropriate analyses. • Report questionable test results and participate in OOS and failure investigations. • Excellent communication skills and professional/technically proficient • Must take the initiative as problems and/or opportunities arise | 11/9/2022 |
| 5792 | Arvinas New Haven, CT Associate Scientist, Platform Biology B.S./M.S. in Biology or related field Exp: 1-4 years |
We are looking for a motivated individual to join our Platform Biology team as an Associate Scientist. This position will be dedicated to conducting experiments and executing assays involving cultured cells or isolated proteins and using multiple methodologies to develop protein degrader small molecules. This is a committed bench scientist position located at our headquarters in New Haven, CT and reports to the Senior Research Investigator in our Platform Biology group. | 11/9/2022 |
| 5793 | Arvinas New Haven, CT Research Associate, Platform Biology B.S./M.S. in Biology or related field Exp: 0.5-2 years |
We are looking for a motivated individual to join our Platform Biology team as a Research Associate. This position will be dedicated to conducting experiments and executing assays involving cultured cells or isolated proteins and using multiple methodologies to develop PROTAC protein degrader small molecules. This is a committed bench scientist position located at our headquarters in New Haven, CT, and reports to a Senior Research Scientist in our Platform Biology group. NOTE: This position is a temporary role to cover an individual while out on maternity leave. This is a terrific opportunity to demonstrate technical capabilities and establish a network within Arvinas for potential future opportunities! | 11/9/2022 |
| 5794 | Atalanta Therapeutics Boston, MA Associate Scientist I/II, In Vitro Biology, Platform Development Bachelor’s degree in a relevant biological science; OR a Master’s degree in biochemistry or relevant biological science Exp: BS: 1 year; MS: 0-2 plus |
Atalanta is seeking a highly motivated individual to join our In Vitro Biology team to contribute to the preclinical development of RNAi-based therapeutics. The selected individual is expected to design and execute biochemical assays for the quantification of therapeutic oligonucleotides, transcriptional profiling while supporting the development of our internal RNAi platform. This role requires a highly collaborative and entrepreneurial mindset that will interact with multiple areas across Atalanta’s research. | 11/9/2022 |
| 5795 | Atalanta Therapeutics Boston, MA Associate Scientist II/Senior Associate Scientist, In Vitro Biology Master’s degree in biochemistry or relevant biological science Exp: 0-2 plus |
Atalanta is seeking a highly motivated Associate Scientist II/Senior Associate Scientist to join our In Vitro Biology team to contribute to the preclinical development of RNAi-based therapeutics. This individual is expected to design and execute assays for the identification of therapeutic oligonucleotides, to assess the knockdown of target mRNAs and proteins and to assess additional molecular biomarkers of therapeutic efficacy. | 11/9/2022 |
| 5796 | Atalanta Therapeutics Boston, MA Associate Scientist II/Senior Associate Scientist, In Vivo Pharmacology Master’s degree Exp: 0-2 plus years |
Atalanta is seeking a highly skilled and motivated Associate/Senior Associate Scientist to join the in vivo pharmacology group to support Atalanta’s drug discovery programs. This individual will extensive hands-on experience in performing survival surgeries (stereotaxic or direct intraparenchymal injection preferred), pharmacological administration, brain and tissue collection, and in processing CNS tissue and molecular analysis to assess target gene and protein expression. We are seeking candidates who thrive in a team-oriented, fast-paced, and cross-disciplinary small biotech environment. The Associate/Senior Associate Scientist will be responsible for assay development and execution of experiments to determine the biodistribution, pharmacodynamic properties and efficacy of oligonucleotides in research and preclinical studies supporting multiple drug discovery programs and platform discovery research. | 11/9/2022 |
| 5797 | Atalanta Therapeutics Boston, MA Associate Scientist/Senior Associate Scientist, Oligonucleotide Chemistry Bachelor’s degree in Chemistry or related scientific discipline Bachelor’s degree in Chemistry or related scientific discipline; -OR- a Master’s degre Exp: BS: 1 year; MS: 0-2 years |
The candidate will join a dynamic team responsible for the design and synthesis of oligonucleotides for Atalanta’s drug discovery programs. Successful candidates will have experience with modern laboratory equipment, and spectroscopic analysis, preferably in relation to oligonucleotides, as well as demonstrated ability to work as part of an integrated team on multiple parallel projects. This individual will be responsible for the independent operation and maintenance of instruments to synthesize, purify, and analyze chemically modified oligonucleotides as well as prepare samples for in vitro and in vivo studies. The ideal candidate is personable, organized, and thrives in a fast-paced environment. This role provides the right candidate with the opportunity to take on increasing responsibility over time within Atalanta’s Chemistry function. | 11/9/2022 |
| 5798 | Atara Biotherapeutics Thousand Oaks, CA Sr. Research Associate / Associate Scientist - Analytical Development Research Associate: BS in Immunology, or biological sciences Exp: 1 year |
The Research Associate or Sr. Research Associate under supervision will be required directly to participating and performing in laboratory activities to support the design, development, and qualification/Validation of bioanalytical methods and cell-based assays for characterization, in-process and lot release testing of engineered T cell drug products and their impurities. This role will be involved in assay optimization and standardization and assay transfer to QC team. Will be expected to perform assay development experiments, document methods and materials, write technical reports and communicate findings. This role is expected in cross-functional collaboration with other departments as needed. | 11/9/2022 |
| 5799 | Atreca San Carlos, CA RESEARCH ASSOCIATE II/SR. RESEARCH ASSOCIATE, IN VIVO PHARMACOLOGY MS Exp: 1+ years |
Atreca is a dynamic biotechnology company whose Immune Repertoire Capture™ technology enables the discovery and development of novel cancer immunotherapeutics. Atreca is looking for a talented and self-motivated SRA/Associate Scientist to join its In Vivo Pharmacology team. The RAII/SRA will apply his/her expertise to Atreca's oncology preclinical research program. The successful candidate will have the opportunity to interact and collaborate with a multidisciplinary team in a dynamic and fast paced scientific environment. In this role, the RAII/SRA will perform multiple efficacy studies testing various therapeutic agents and combination regimens in mouse tumor models. Job title/compensation commensurate with experience and qualifications. | 11/10/2022 |
| 5800 | Avance Biosciences Houston, TX Laboratory Associate II Bachelor’s degree in biological sciences Exp: 1 year |
Carry out Molecular Biology, Microbiology, Protein experiments following established SOPs and/or guidance of laboratory management. Perform DNA/RNA extraction, quantification, and gel QC. Perform PCR setup for qualitative and quantitative analysis Report experimental results to project managers in a timely manner. Follow established quality management policies and GLP and GMP practices. | 11/10/2022 |
| 5801 | Sorrento Therapeutics San Diego, CA QC Microbiology Associate Bachelor’s degree in Microbiology (or equivalent education/experience) Exp: 1-2 years |
Provide microbiological support and testing of cGMP environments as well as contributing to WFI testing, bioburden and sterility testing. | 10/30/2022 |
| 5802 | Sorrento Therapeutics San Diego, CA Research Associate Bachelor's Degree in Life Sciences or a related field. Exp: 0-2 years |
Sorrento Therapeutics (“Sorrento”) is seeking a Research Associate who, under close supervision assists in conducting laboratory experiments, maintain laboratory environment, organizing data, and analyzing results. Major tasks include: antibody discovery by phage display, antibody expression and purification, antibody characterization, cell culture and cell based assay | 10/30/2022 |
| 5803 | Sorrento Therapeutics San Diego, CA Research Associate - Process Development & Manufacturing Bachelor’s Degree in Molecular Biology or related disciplines Exp: 0-2 years |
Sorrento Therapeutics (“Sorrento”) is seeking a Process Development and MFG Research Associate position to help with protein production and DNA plasmid cGMP production in microbial system including process development and manufacturing. Major tasks include: Buffer preparation, bacteria culture including fermentation in bioreactor and harvest, bacteria lysis and protein and plasmid DNA purification. | 10/30/2022 |
| 5804 | Swift Biosciences Danvers, MA Research Associate IHC BSc or BA in a Scientific discipline Exp: 1 to 4 Years |
Research Associates are responsible for the undertaking of research and development activities to support contracted pharma projects to develop companion diagnostics IVDs. The Research Associate will be responsible for performing required laboratory studies, including making observations, reporting data and providing results to support key decisions within the Pharma Partnerships business unit. A shown ability to communicate (verbal and written) and work with all levels of staff is fundamental to this role. Ensure all work is conducted in accordance with applicable protocols and work instructions and that all work is appropriately documented per procedure | 10/31/2022 |
| 5805 | Swift Biosciences Carlsbad, CA Development Scientist I Bachelor of Science degree in Biology, Microbiology, Chemistry, Biochemistry or related science Exp: 0+ years |
The Development Scientist I for Beckman Coulter Diagnostics is responsible for helping to Develops methods for the production and testing of new products. Develops new product designs, processes, new product scale-up, design/product optimization, technology transfer and process/product validation activities. Develops production procedures and process/product specifications. This individual will perform experimental studies, collect and evaluate the data, and communicate the results towards this goal. In addition, this individual will support both continuous improvement activities and current market products. This position is part of Research & Development located in Carlsbad, CA and will be On-Site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. | 10/31/2022 |
| 5806 | Tara Biosystems Lexington, MA Associate Scientist, High-throughput Medicinal Chemistry BS or MS in Chemistry, or related subject Exp: 0 – 2 years |
We are looking for a highly motivated chemist to join our High Throughput Medicinal Chemistry teams. This individual will be responsible for the synthesis of small molecules (singletons & libraries) in support of our Medicinal Chemistry programs. | 10/31/2022 |
| 5807 | Tectonic Therapeutic Watertown, MA Research Associate/Senior Research Associate – Protein Sciences (Protein Biophysics) Bachelor’s or Master’s degree in analytical or biophysical chemistry or related discipline Exp: 1-3 years 1-3 years 1-3 years |
The (Senior) Research Associate for Tectonic will be a highly collaborative team player who has experience characterizing proteins using a wide array of analytical and biophysical techniques. Hands-on experience with standard biophysical techniques is required and experience with assay development is a plus. The successful candidate will contribute to our core research capabilities and the development of our anti-GPCR antibody discovery platform. The candidate would conduct established biophysical assays and perform continuous development and improvement over time. This position represents a unique opportunity for the successful applicant to join an innovative start-up at the heart of the Boston biotech ecosystem and to contribute to its long-term Success. | 10/31/2022 |
| 5808 | Thrive Earlier Detection Madison, WI Research Associate I, Advanced Research and Technology Bachelor’s degree in Life Sciences, Medical Technology, Clinical Laboratory Science, Chemical/Physical/Biological Science, or related field. Exp: 1+ years |
The Research Associate I, with guidance from more experienced scientists, assists in the day to day experimental work that includes execution of bench experiments, and gathering and assembling of data. Working in a team setting, the Research Associate I will primarily be involved in Research and Development projects assisting in translating research ideas and concepts into the product development pipeline towards development of diagnostic assay products. | 11/1/2022 |
| 5809 | Thrive Earlier Detection Cambridge, MA Research Associate I Research Associate I Research Associate I Bachelor’s degree in Life Sciences, Medical Technology, Clinical Laboratory Science, Chemical/Physical/Biological Science, or related field. Exp: 1+ years |
The Research Associate I, with guidance from more experienced scientists, assists in the day to day experimental work that includes execution of bench experiments, and gathering and assembling of data. Working in a team setting, the Research Associate I will primarily be involved in Research and Development projects assisting in translating research ideas and concepts into the product development pipeline towards development of diagnostic assay products. | 11/1/2022 |
| 5810 | Trevigen San Marcos, CA Research Associate - Advanced Bachelor’s degree in Chemistry, Biochemistry, Biological Science, or related field preferred Exp: 1-5 years |
Responsible for developing controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for developing quality products on schedule. General knowledge and basic application of concepts, theories, terminology and practices that apply to research in a laboratory environment. | 11/1/2022 |
| 5811 | Trevigen Minneapolis, MN Research Associate, Microbiology QC Bachelor’s degree in Microbiology or a related scientific field or equivalent Exp: up to 3 years |
The responsibilities of this position are to participate in the Microbiology QC testing and reporting procedures: set up, read, and report the microbial QC bioburden and sterility testing of various sample types using culture methods that include direct plating, broth inoculation, and membrane filtration. Performance of environmental monitoring for viable microbes, particle counts, and WFI/deionized water testing, reading, and reporting. Assist with efficacy and validation testing, new procedure development, new equipment IQ/OQ and calibrations. Perform general lab duties, assist with sanitization of clean rooms, and additional duties as assigned. | 11/1/2022 |
| 5812 | Universal Cells Seattle, WA Research Associate II, Process Development MS Exp: 0-2 years |
The primary purpose of the Research Associate II for Process Development is to execute experiments to improve clinical-grade, gene-editing processes of Universal Donor Cells and to provide data for CMC documents. This Research Associate II role will work as part of a team evaluating processes, and planning/executing experiments to evaluate all aspects of culturing, gene-editing, and processing of pluripotent stem cells. This position will be provided training to perform all required fundamental skills. Will assist with complex laboratory operations, keep appropriate documentation including lab notebooks, batch documentation and experimental summaries. Will be able to execute protocols with minimal guidance and will have the ability to summarize results independently. May assist in generating content and preparing controlled documents and data summaries. This position will acquire further versatility in routine procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. | 11/1/2022 |
| 5813 | VaxCyte San Carlos, CA Associate Scientist I/II, Analytical Development for Characterization MS in Chemistry, Analytical Chemistry preferred, Organic / Biochemistry considered. Exp: 1-3 years |
Vaxcyte is looking for an energetic and talented individual to join our Analytical Development team. Primary responsibility for the incumbent will be to support the developmental activities currently on going in the laboratory as assigned. | 11/1/2022 |
| 5814 | VGXI The Woodlands, TX DOWNSTREAM PROCESS TECHNICIAN Bachelor’s or Associate's degree or equivalent from college or technical school. Exp: 0-3 years |
Responsible for manufacturing revolutionary clinical and commercial nucleic acid based pharmaceuticals by interfacing with manual and automated production systems and controls in cGMP manufacturing environment while maintaining areas in a state of compliance with internal quality systems. Follows standard operating procedures to operate production equipment for downstream operations. Maintains records, process and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for proficiency in assigned functional area: Downstream Manufacturing. Understands and applies biological, chemical and mechanical principles and techniques. | 11/2/2022 |
| 5815 | VGXI The Woodlands, TX UPSTREAM PROCESS TECHNICIAN Bachelor’s or Associate's degree or equivalent from college or technical school. Exp: 1-3 years |
Responsible for manufacturing revolutionary clinical and commercial nucleic acid based pharmaceuticals by interfacing with manual and automated production systems and controls in cGMP manufacturing environment while maintaining areas in a state of compliance with internal quality systems. Follows standard operating procedures to operate production equipment for upstream operations. Maintains records, process and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for proficiency in assigned functional area: Upstream Manufacturing. Understands and applies biological, chemical and mechanical principles and techniques. | 11/2/2022 |
| 5816 | VGXI The Woodlands, TX MICROPROCESS TECHNICIAN Bachelor’s or Associate's degree or equivalent from college or technical school. Exp: 1-3 years |
Responsible for manufacturing revolutionary clinical and commercial nucleic acid based pharmaceuticals by interfacing with manual and automated production systems and controls in cGMP manufacturing environment while maintaining areas in a state of compliance with internal quality systems. Follows standard operating procedures to operate production equipment for plasmid manufacturing operations. Maintains records, process and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for proficiency in assigned functional area: Microprocess Manufacturing. Understands and applies biological, chemical and mechanical principles and techniques. | 11/2/2022 |
| 5817 | WaVe Life Sciences Cambridge, MA Research Associate/Scientist, Biology BS or MS degree in biology, biochemistry, cellular/molecular biology or related discipline Exp: |
Wave seeks a highly motivated biologist to join its research team in Cambridge, Massachusetts to support a rapidly expanding RNA-editing platform. This is an ideal position for an individual who is interested in working with cutting edge technologies and who thrives in a team-oriented, fast-paced, and cross-disciplinary biotech environment. The candidate should have strong technical skills, and will be responsible for designing, executing, and analyzing experiments as a member of team focused on advancing therapeutic programs and discovery research platforms. | 11/2/2022 |
| 5818 | Frontage Hayward, CA Research Associate-Bioanalytical M.S. degree in related scientific discipline or B.S degree Exp: 0-3 years |
1)Execute established protocols and methods to assay small molecule compounds, their metabolites, and impurities in various chemical and biological samples. 2)Perform data analysis on LC/MS and HPLC instruments, with the ability to identify and troubleshoot inconsistencies as needed. 3) Perform analytical, pharmacokinetic/pharmacodynamic, metabolism data analysis. 4) Conduct basic method development and validation studies. 5) Conduct trouble-shooting and instrument maintenance of LC/MS. 6) Present and discuss data internally and externally. 7) Write reports under supervision. | 11/2/2022 |
| 5819 | Frontage Hayward, CA Research Associate-Biologics MS / MA in biochemistry, biology, chemistry, pharmaceutics or related scientific discipline Exp: 0-2 years |
Conduct study design, lab-testing, data analysis and PI review. Author and/or review methods, protocols and other related documents. Assist PIs in maintaining project quality, meeting compliance requirements and timelines. Prepare notebooks, study binders, data packets, data summaries, methods, and qualification/validation protocols under the supervision of lab management / PIs Monitor reagent and consumable inventories and timely submit the orders for the support of both project and non-project based programs After receiving sufficient training, perform as PI and manage the overall planning, execution, and quality of assigned MD/MV and sample analysis projects under the supervision of lab management Participate TC and communicate with sponsors to solve technical issues and update projects, provide weekly summary to the sponsorsConduct study design, lab-testing, data analysis and PI review. Author and/or review methods, protocols and other related documents. Assist PIs in maintaining project quality, meeting compliance requirements and timelines. Prepare notebooks, study binders, data packets, data summaries, methods, and qualification/validation protocols under the supervision of lab management / PIs Monitor reagent and consumable inventories and timely submit the orders for the support of both project and non-project based programs After receiving sufficient training, perform as PI and manage the overall planning, execution, and quality of assigned MD/MV and sample analysis projects under the supervision of lab management Participate TC and communicate with sponsors to solve technical issues and update projects, provide weekly summary to the sponsors | 11/2/2022 |
| 5820 | Frontage Hayward, CA Research Assistant-ADME BS in biology, biochemistry and other related fields Exp: 0-3 years |
We are looking for a highly-motivated Research Assistant to develop and conduct biochemical and cellular assays to evaluate potential therapeutics. Experience in cell line development, ELISA, PBMC biomarker, cell culture, cellular assays, gene expression is desirable. Prior experience in ADME assays including metabolite stability, drug transporter, CYP450, PPB and measurements of physicochemical properties is preferred. The candidate needs to be proficient in assay design, trouble-shooting, data analysis and working with 96-w & 384-w plate-based assays. The candidate needs to have a good understanding of drug discovery processes and experience in a discovery project is preferred. This position requires working with an interdisciplinary team of DMPK scientists, analytical chemists and pharmacologists. | 11/2/2022 |
| 5821 | Frontage Hayward, CA Research Associate M.S. degree in related scientific discipline. Exp: 0-3 years |
1) Perform Watson design according to Study Protocols 2) Conduct basic method development and validation studies. 3) Ability to troubleshoot and solve basic technical and instrumental issues. 4) Conducts and documents work in a regulated environment. 5) Reviews the data package and notebooks for junior chemists 6)Writing up analytical methods, protocols, and reports under supervision 7) Perform project communication with client, study director, and project management team under supervision | 11/2/2022 |
| 5822 | Frontage Exton, PA Associate Scientist, Pharmaceutical Analysis, Small Molecule B.S. in Chemistry or related discipline Exp: 1-2 years |
Performs routine sample analysis and a variety of tasks to support product development, ensuring agreed timelines Assists method development Performs method validation under supervision Reports and resolves any unexpected issues under supervision Complies with all relevant cGMP and/or GLP regulatory requirements while carrying out assigned studiesPerforms routine sample analysis and a variety of tasks to support product development, ensuring agreed timelines Assists method development Performs method validation under supervision Reports and resolves any unexpected issues under supervision Complies with all relevant cGMP and/or GLP regulatory requirements while carrying out assigned studies | 11/2/2022 |
| 5823 | Frontage Exton, PA Associate Scientist/scientist Associate Scientist/scientist M.S. or a B.S./B.A. Exp: 1-5 years |
This is a technical scientific position within the Biologics Service Team. The Biologics Service Team is responsible for conducting bioanalytical methods related to large molecule biotherapeutic drug development across all therapeutic areas, spanning nonclinical studies to post-market clinical development. | 11/2/2022 |
| 5824 | Frontage Exton, PA Scientist/Associate Scientist- Cell Culture B.S. or M.S. in molecular biology, biochemistry, biophysics, immunology, or a related field Exp: 1 year |
This is a bench scientific position for a competent and hardworking scientist with experience in protein purification and/or labeling of protein reagents. The person will be responsible labeling of reagents (protein and antibodies), purification and characterization including concentration estimation, SDS-PAGE, SE-HPLC, endotoxin estimations etc. He/she will be responsible for the quality of final product, record keeping and interacting with end user. The position will require excellent communication skills, and basic computer skills. | 11/2/2022 |
| 5825 | Inotiv Rockville, MD Associate Scientist I (In Vitro Cytogenetics) Bachelor’s degree in a scientific discipline (i.e., Biology, Chemistry, Biochemistry, etc.) Exp: 1+ years |
Perform a wide variety of in vitro assays or tests required to characterize product or material safety Maintain sterile and good cell/tissue culture techniques Prepare study reagents in accordance with SOPs and study instructions Use and maintain scientific equipment, instrumentation and computer systems Conduct pre-designed assays using basic laboratory techniques and skills Make scientific observations, maintain detailed data books/documentation and ensure all documentation fulfills generally accepted professional/industry standards and GLP regulations Perform peer review of data and lab support records Keep the next level manager and Study Director informed of study status, technical problems and other issues which impact the lab/study Address quality audit findings and generate deviations using the quality system, as needed Receive instructions on new assignments from the laboratory manager or designee and study directors Attend pre-planning, or operational team meetings, as needed Perform other job duties, as assigned | 11/2/2022 |
| 5826 | Inotiv West Lafayette, IN Bio Analyst I B.S. in chemistry or biology Exp: one year |
Conducts sample analysis with data interpretation and basic troubleshooting. Conducts method development and method validation experiments. Assists with general housekeeping and assist other departmental personnel as necessary. | 11/02/2022 |
| 5827 | Inotiv Raleigh, NC Research Assistant A.S. or B.S. in biology or related field Exp: 0-3 years |
The Genetic Toxicology Group conducts standard and custom genetic toxicology testing and applied research supporting preclinical studies for both federal and commercial clients. | 11/02/2022 |
| 5828 | A2 Biotherapeutics Los Angeles, CA Research Associate, Drug Discovery Master’s or Bachelor’s degree in science including biology, immunology, biotechnology, or a related discipline Exp: 1-2 years |
The Drug Discovery team is seeking a highly motivated individual with experience in biochemistry, cell and molecular biology, and assay development. This is a rare opportunity to directly contribute to enabling gene therapies in broader and more challenging indications. The successful candidate will work at our research facility in Agoura Hills, CA and collaborate across multiple projects. You will join a fast-paced, dynamic and team-oriented environment and will benefit from cutting-edge scientific training, career growth, and publishing opportunities. | 11/02/2022 |
| 5829 | Abbott Scarborough, ME Reagents Scientist I Reagents Scientist I Bachelor's degree (BA or BS) in biology, immunology, or chemistry or equivalent combination of education and experience. Exp: 1-year |
The position of Reagent Scientist I is within our Abbott Rapid Diagnostics business located in Scarborough, Maine. This role will include producing antibodies for use in immunology-based chromatography and enzyme tests. The primary responsibility of the individual is the production and maintenance of the Technical Manufacturing Critical Reagent supply using Standard Operating Procedures (SOPs). | 11/3/2022 |
| 5830 | Abbott Scottsdale, AZ Electrical Engineer I Electrical Engineer I Bachelors Degree (± 16 years) Electrical/electronic engineering or related engineering field OR an equivalent combination of education and work experi Exp: six months |
Electrical Engineer I Performs entry-level activities to design and develop the layout, construction, and evaluation of a variety of prototype Printed Circuit Boards, fixtures, and tools. Identifies and routinely uses the most effective and cost-efficient business practices to execute processes. Promotes the process of continuous quality improvement and risk management and coordinates solutions for technical and project issues. Applies engineering and scientific principles to the evaluation and solution of technical problems. Exercises independent judgment in planning and organizing work; monitors performance and reports status. Identifies and routinely uses the most effective, cost efficient and best practices to execute processes; continually evaluates their effectiveness and appropriateness. | 11/3/2022 |
| 5831 | Abbott Plymouth, MN R&D Engineer I R&D Engineer I Bachelor’s degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, biological sciences, medical/clinical science or equivale Exp: 1+ years’ |
As R&D Engineer I, at our Plymouth, MN or St. Paul, MN location, you will be part of our Electrophysiology (EP) product development team focused on delivering the future in diagnostic, imaging, and ablation therapy catheters and EP capital equipment. This role will involve a range of responsibilities including but not limited to requirement development, testing and data analysis, and test method development and validation. | 11/3/2022 |
| 5832 | AbbVie Worcester, MA Associate Scientist I/II - Pipeline (New Grads) Bachelor’s Degree or Master’s degree. Exp: Recent Graduate |
We welcome recent graduates to apply for the Associate Scientist position, where you will generate and analyze precise, reliable, and reproducible data in a timely manner, under the direction of a more senior scientific leader. Demonstrate experimental precision and should possess general understanding of core discipline. | 11/3/2022 |
| 5833 | Associates of Cape Cod East Falmouth, MA Quality Control Analyst I B.S. degree in a relevant scientific discipline Exp: 0-2+ years |
In this role you will perform chemical and/or biological assays of commercial product raw materials, production intermediate and bulk samples, finished product, environmental monitoring samples, process and cleaning validation samples. Assays are qualitative, quantitative and investigational in nature and are performed in compliance with cGMP, ACC SOPs, and FDA Analyst has working knowledge of relevant QC techniques, policies and procedures to perform QC tasks and document results. Analyst receives minimal supervision on routine assignments and detailed instructions on new assignments. | 11/3/2022 |
| 5834 | Adaptimmune Therapeutics Philadelphia, PA Manufacturing Cell Therapy Specialist Bachelor degree in a cell biology, bioengineering or medical technology related field, or equivalent experience is required. Exp: 1+ years’ |
This role will provide support for the manufacturing of gene modified autologous T-cell product at our manufacturing site in the Philadelphia Navy Yard. The Specialist will perform cell processing activities, media formulation, product sampling, and other manufacturing needs as necessary, commensurate with the level of training and experience of employee. Work is primarily in Grade B and Grade C aseptic manufacturing environment, but may also include support of process development runs in the Manufacturing Science and Technology laboratory. | 11/3/2022 |
| 5835 | Adare Pharmaceuticals Vandalia, OH QC Analyst Bachelor degree in Chemistry or related field Exp: 0 to 3 years |
The essential job function is to perform physical and chemical testing of intermediate and finished products according to written procedures. | 11/3/2022 |
| 5836 | Adare Pharmaceuticals Vandalia, OH QC Analyst (Night Shift) Bachelor degree in Chemistry or related field Exp: 0 to 3 years |
The essential job function is to perform physical and chemical testing of intermediate and finished products according to written procedures. | 11/3/2022 |
| 5837 | Admera Health South Plainfield, NJ Associate Scientist I/II Bachelor’s degree or M.S. in Biological Sciences Exp: 1-3 years |
• Preparing solutions and reagents for performing assays on the bench. • Perform Next Generation Sequencing-based genomic assays on different workflows (few listed below): o RNAseq o Whole Genome Sequencing o Whole Exome Sequencing • Carry out genomic assays under Biosafety Level II Policies and in regulatory compliance. • Perform Operational Qualification and Performance Qualification on Next Generation Sequencers. | 11/3/2022 |
| 5838 | Akoya Biosciences Marlborough, MA Quality Engineer, Reagents Bachelor’s Degree in Chemistry, Biology, Engineering, or a related field Exp: 1-4 years |
Akoya Biosciences is looking for a Quality Engineer to join our Quality team. The individual will manage a variety of quality system functions of Akoya Biosciences’ growing Quality Management System (QMS), working with Quality Management, product development, manufacturing, operations, and other groups, to ensure compliance to ISO 13485 and medical device quality requirements. The individual must be able to work independently and resolve or escalate quality issues in a creative, collaborative, and timely manner. Core values must include commitment to customer and operations excellence with demonstrated ethics and integrity. The Quality Engineer will manage day-to-day QMS processes such as Document Control, Change Control, Training, Supplier monitoring, CAPA, Nonconformances, and generating metrics. The individual will also help develop new processes as the QMS grows and participate in implementing a new electronic QMS system. The Quality Engineer will also participate in design quality, auditing, and will have opportunities to grow within the Quality group. This includes learning about and supporting the laboratory testing quality activities as needed. | 11/4/2022 |
| 5839 | Akron Biotechnology Sarasota, FL Manufacturing Associates (I, II, III) BA/BS or AA/AS in Biology, Chemistry, Bioengineering or a related field. Exp: 1-2 years’ |
Akron Biotech is continuing to transform and further its rapidly growing capabilities and is now seeking highly motivated professionals to join our expanding team. This is an exciting opportunity to play a critical role within our organization that is driving advanced therapy development and commercialization with high quality industrial scale solutions. We manufacture and distribute components and raw materials for cell therapy discovery, development, and commercialization to meet industry needs worldwide. We offer an array of highly competitive benefits and perks to our valued associates. Candidates will be placed as I, II and III according to the degree of knowledge and experience they possess to support, perform, and/or supervise CGMP operations. A MFG Associate III is a person with sufficient and demonstrated skills, knowledge, and experience at process Unit of Operations in a CGMP environment, while the MFG Associate I requires just the proven and correct background education. | 11/4/2022 |
| 5840 | Alcami Morrisville, NC Associate Scientist I, Micro/Environmental Monitoring Bachelor’s degree in Microbiology or similar field Exp: no related experience required |
The Associate Scientist I is accountable for driving results in a fast-paced environment by performing complex microbial analysis and assisting with method development and validation. The Associate Scientist I may assist in GMP review, provide problem solving support and Laboratory Investigation Report ownership for the Microbiology Department. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 11/4/2022 |
| 5841 | NantKwest Culver City, CA Research Associate Research Associate Research Associate B.S. in biochemistry or in related scientific disciplines Exp: up to 2 years |
ImmunityBio Inc. is seeking a highly motivated, full-time research associate to join the Protein Science group to support the discovery, research and development of immunotherapies across multiple therapeutic areas, including, but not limited to cancer and infectious diseases. The ideal candidate should have a bachelor’s degree with 1-2 years of wet-lab experiences, ability to manage multiple tasks in a timely manner, good written/verbal communication skills and have a willingness to work as part of the team. | 10/25/2022 |
| 5842 | NJ Biopharmaceuticals Princeton, NJ Associate Scientist B.S. in Chemistry Exp: 0-5 years’ |
Under department supervision, plan, setup, monitor and workup chemical reactions and isolate product; optimize reaction conditions for improved yields and outputs; purify compounds by different methods; characterize and identify compounds using MS and NMR; maintain a detailed lab notebook; carry out literature searches and mine information for ongoing work from search engines; maintain equipment, chemical inventory, and provide lab support; run multiple reactions daily and provide data in a detailed report; Plan and execute daily and weekly schedule; perform safe lab practices; comply with Site safety protocols and Site Standard Operating Procedures (SOPs). Perform duties as required | 10/25/2022 |
| 5843 | NJ Biopharmaceuticals Princeton, NJ Associate Scientist/Senior Associate Scientist B.S. in Biochemistry, Protein Chemistry, or other related fields Exp: 0-5 years’ |
Under department supervision, plan, setup, monitor and purify bioconjugation reaction using aseptic techniques; characterize and identify bioconjugates using LC-MS, HPLC and/or Capillary Electrophoresis; maintain a detailed lab notebook; maintain equipment, and provide lab support; provide data in a detailed report; Plan and execute daily and weekly schedule; perform safe lab practices; comply with Site safety protocols and Site Standard Operating Procedures (SOPs). Perform additional duties as required. | 10/25/2022 |
| 5844 | NJ Biopharmaceuticals Princeton, NJ QC Scientist (I, II, III, IV, Senior, Principal) BS, MS, or PhD degree in chemistry, biology, biochemistry, or related discipline. Exp: 0-10 years |
Perform all work in a safe and compliant manner in accordance with EHS best practices and cGMP guidelines. Work with management and vendors to acquire, install, and qualify new equipment. Maintain, clean, calibrate, troubleshoot, and repair analytical instruments and equipment. Develop and execute analytical methods for small molecules, proteins, and antibody drug conjugates. Analysis of raw materials, in-process samples, finished products and stability samples by various analytical instruments and document the results under GMP settings. Prepare standard operating procedures (SOPs), analytical test methods, protocols, reports, etc. as needed. Conduct OOS, risk assessment, and root cause investigations and/or assist management with these investigations. Write deviations, change controls, and CAPAs, and/or assist management with these documents. Document work in laboratory notebooks and logbooks according to organizational GDP policies. Write, review, and execute of analytical protocols & reports for method transfers, qualification, and validations in GMP setting. Manage work outsourced to third-party analytical and metrology service providers. | 10/25/2022 |
| 5845 | Oakwood Labs Oakwood Villiage, OH Chemist Bachelor’s degree in chemistry, biology, or related discipline Exp: entry level |
This is an excellent entry level opportunity for those interested in working at a technology-based pharmaceutical company. There will be on the job training rotations in the research and development lab and the quality control chemistry lab. You will gain hands-on experience analyzing and interpreting data for excipients, polymers, active ingredients, and finished pharmaceuticals utilizing advanced analytical instrumentation. You will work as part of small multi-disciplinary technical teams on both immediate and sustained release drug development projects in various stages of development including early proof of concept, supporting pharmacokinetic and clinical studies, technical transfer activities, and supporting commercial product manufacturing. You will have direct input on solving complex problems and contributing to project success. Become part of the Oakwood Labs team and advance your career with an industry leader in injectable pharmaceutical development. | 10/26/2022 |
| 5846 | Oakwood Labs Oakwood Villiage, OH Chemical Engineer/ Biomedical Engineer Bachelor of Science, Masters, or PhD Degree in Biomedical or Chemical Engineering, or Chemistry or closely related science field with chemistry and ma Exp: entry-level |
This is an excellent entry-level opportunity for those interested in working at a technology-based pharmaceutical company. | 10/26/2022 |
| 5847 | Ocugen Malvern, PA Associate Research Scientist, Drug Substance Development Masters in Pharmaceutical Sciences, Molecular Biology, Chemistry, Biochemical engineering or in a related life-sciences field or related disciplines Exp: + 1 year |
Key responsibilities for this role include supporting the cell therapy manufacturing process, production of recombinant protein, and AAV expression in mammalian host systems. You will support the Upstream process (USP) and downstream process (DSP) scale-up to support early and late-stage projects. You will support Process Development of the pipeline projects for pre-clinical and clinical applications, allowing for Tech transfer and scale-up at CDMO partners. Ocugen’s pipeline consists of biological and gene therapy products of varying modalities which include Adenovirus assets for Vaccines, AAV for gene therapies and regenerative medicine asset for knee cartilage repair | 10/26/2022 |
| 5848 | Ortho Dermatologics Bothell, WA Quality Assurance Specialist I (WA) Quality Assurance Specialist I (WA) Quality Assurance Specialist I (WA) 4 years bachelor level degree in Science, engineering or other similar discipline. Exp: 1-3 years |
The Quality Assurance Specialist I will perform complaint investigation activities for product complaints and Adverse Events with cross functional team members and provide complaint investigation reports in compliance with Solta procedures, Food and Drug Administration (FDA), International Standards Organization (ISO), Quality System requirements, and other regulatory guidelines. | 10/26/2022 |
| 5849 | Pacific BioLabs Hercules, CA Microbiology Laboratory Analyst I/II An undergraduate or AA degree in a science-related field (e.g., Microbiology, Biological Sciences). Exp: 0-3 years |
PBL has immediate openings for full or part time Microbiology Laboratory Analysts in the Microbiology Services Department. The Microbiology Laboratory Analyst will report to Microbiology Management and will contribute to general laboratory testing, sample management, and laboratory maintenance. The Microbiology Laboratory Analyst is expected to participate with the team to meet Microbiology Services Department goals and perform routine laboratory duties as directed. | 10/26/2022 |
| 5850 | Patheon Florence, SC Scientist I - Process R&D BS/BA degree in chemistry or BS in science Exp: 0-3 years |
This is an entry-level opportunity to support the Process R&D efforts at the Florence, SC facility. | 10/27/2022 |
| 5851 | Patheon Florence, SC QC Scientist I Bachelor's degree in physical science, preferably in a life science discipline Chemistry or Biology. Exp: 0-2 years |
Provides analyses in an analytical chemistry environment within defined procedures and practices. Performs analytical methods for moderately sophisticated testing on raw materials, in-process samples, stability, and final release for APIs. Supports internal development and/or manufacturing operations. Makes detailed observations and reviews, documents, and communicates test results; recommends solutions. | 10/27/2022 |
| 5852 | Patheon Cambridge, MA QC Scientist I Bachelors degree B.S. in Chemical Engineering, Biochemistry, Biology or related field Exp: 1-2 years |
Position is Sunday-Wednesday 7:30 AM to 6:00 PM. The QC Scientist I will perform routine environmental monitoring, critical utility testing, and microbiological assays. Completes method suitability testing and writes final reports. The incumbent will act as a leader in the lab helping management to interview and train junior employees, schedule testing, troubleshoot assays and equipment, and act as a SME during internal and external audits. | 10/27/2022 |
| 5853 | Patheon Cambridge, MA QC Scientist I Bachelor’s degree B.S. in Chem Eng, Biochemistry, Biology, or related field Exp: 1-2 years |
Position is Wednesday-Saturday 9:00 pm-8:30 am. The QC Scientist I will perform routine environmental monitoring, critical utility testing, and microbiological assays. Completes method suitability testing and writes final reports. The incumbent will act as a leader in the lab helping management to interview and train junior employees, schedule testing, troubleshoot assays and equipment, and act as a SME during internal and external audits. | 10/27/2022 |
| 5854 | Patheon Cambridge, MA QC Scientist I Bachelors degree B.S. in Chem Eng, Biochemistry, Biology or related field Exp: 1-2 years |
Position is Sunday-Wednesday 9:30 PM-8:00 AM. The QC Scientist I will perform routine environmental monitoring, critical utility testing, and microbiological assays. Completes method suitability testing and writes final reports. The incumbent will act as a leader in the lab helping management to interview and train junior employees, schedule testing, troubleshoot assays and equipment, and act as a SME during internal and external audits. | 10/27/2022 |
| 5855 | Patheon San Diego, CA Scientist I, Manufacturing Sciences Bachelor’s degree, in Molecular Biology, Biology, Biochemistry, Chemistry or Material Science Exp: 1+ years |
The Scientist I will support within the Technical Operations Organization in the in vitro medical diagnostics device manufacturing setting. The ideal candidate will execute experiments to support in-process assay development, process improvement with the goal of increasing product quality, consistency, and yield. Typically, this team is focused on experimental, QC, and field data for analysis, trending, and translation into root cause analysis. | 10/27/2022 |
| 5856 | Eurofins Lancaster Laboratories New Berlin, WI Chemist I Bachelor's degree in chemistry or related field Exp: 1-2 years |
Eurofins is searching for a Chemist I in New Berlin, WI. The Chemist I receives sufficient authority from, and is accountable to, the Environmental Lab Supervisor or Monograph Team Lead, or appointed designate, for the successful completion of assigned duties and responsibilities and has the authority to take action necessary to carry out the duties and responsibilities of this position and to identify the occurrence of departures from the quality system or from the procedures for performing tests and/or calibrations, so long as such action does not deviate from established company guidelines, is consistent with sound technical and business judgment, and follows the practices of the laboratory. | 10/27/2022 |
| 5857 | Pliant Therapeutics South San Francisco, CA Research Associate/ Sr. Research Associate, DMPK Research Associate/ Sr. Research Associate, DMPK BS/MS degree in biochemistry, pharmaceutical science, or related scientific discipline Exp: 1-4 years |
Pliant Therapeutics seeks a highly motivated, team-oriented, and importantly, scientifically curious individual for the position of Senior Research Associated in the department of Drug Metabolism and Pharmacokinetics. The successful candidate will be responsible for conducting routine and custom in vitro ADME assays, with emphasis on permeability and transporter related assays, leveraging a solid experience in LC-MS/MS bioanalytical techniques to support drug discovery and development programs. | 10/27/2022 |
| 5858 | Pliant Therapeutics South San Francisco, CA Research Associate Scientist II, Biochemistry and High Throughput Screening BS or MS, in Biochemistry, Cellular Biology or related field Exp: One to three years’ |
Immediate opening available for Biologist/High Throughput Screening Research Associate Scientist. This individual will join a dynamic and growing multidisciplinary team focused on discovery and advancement of new drug candidates and disease biomarkers. The successful candidate will work under the direct supervision of a Senior Scientist or Scientist. | 10/27/2022 |
| 5859 | PolyPeptide Group San Diego, CA Production Chemist I BS in Chemistry, Biochemistry, Biology or related field Exp: 1+ years |
Checks reactor system for proper operation in accordance with SOP and/or operation manual. Under general supervision and direction, measures and mixes ingredients according to the BPR (Batch Production Record). Dispensing of raw materials from Pharmastore for Synthesis. During processing, monitors chemical reactions (color and completeness of chemical reactions) and under general direction of supervision and/or senior Production Chemist personnel responds with appropriate actions to ensure proper processing. Using established procedures (safety and process) and under general supervision, performs intermediate chemical processing steps. | 10/27/2022 |
| 5860 | Poseida Therapeutics San Diego, CA Research Associate, Immuno-Oncology Master's or Bachelor's degree in a Scientific discipline Exp: up to 2 years |
Poseida is seeking an outstanding candidate to join our immuno-oncology team. The Research Associate will support the development of chimeric antigen receptor (CAR-T) cellular therapies against cancer and will be involved in bench work, laboratory studies, and the coordination of research projects with the assistance of their manager or a senior lab member. | 10/27/2022 |
| 5861 | Poseida Therapeutics San Diego, CA Research Associate - Immuno-Oncology (CAR-T) BS in in the field of immunology, molecular biology, or related field Exp: 0-plus years |
Poseida is seeking an outstanding candidate to join our Immuno-Oncology team. The Research Associate will support the development chimeric antigen receptors (CAR-T) cellular therapies against cancer, and possibly other disease areas. Primary responsibilities will involve isolation of primary lymphocytes for pre-clinical research and coordination of blood product, and other raw material, inventory, characterization, and testing. Additional responsibilities may include designing and performing experiments, organizing and sharing data, and the coordination of research projects in a highly collaborative team setting, with the assistance of your manager | 10/27/2022 |
| 5862 | Poseida Therapeutics San Diego, CA Research Associate/Senior Research Associate, Gene-edited T Cell Therapies Research Associate I: Master's or Bachelor's degree in a Scientific discipline Exp: 0-2 years |
Poseida is seeking an exceptional Research Associate or Senior Research Associate to join our Immuno-Oncology team. The position will utilize NGS and other molecular biology techniques for rigorous molecular characterization of allogeneic CAR-T cells generated using Poseida’s proprietary and highly specific Cas-CLOVER gene-editing system. This position will support the Immuno-Oncology CAR-T cell therapy pipeline as well as other gene-editing platform improvement efforts. Primary responsibilities will include designing and performing experiments, organizing and sharing data, and coordinating research projects in a highly collaborative team setting. The ideal candidate will be highly motivated, detail oriented, and possess a high level of scientific rigor.\ | 10/27/2022 |
| 5863 | Poseida Therapeutics San Diego, CA Research Associate/Research Associate II, In Vivo Gene Therapy BS/MS in the field of biochemistry, molecular biology, biology or related field Exp: 6 months plus years |
Poseida Therapeutics is seeking a talented and self-motivated research associate to join our In Vivo Gene Therapy team. This position offers an excellent opportunity for a team-oriented, independent individual to assist in the pre-clinical development of novel in vivo gene therapies. | 10/27/2022 |
| 5864 | Prominex San Diego, CA Research Associate I/II Master’s degree in Science Exp: 0-2 years |
Prominex Inc. is a startup molecular diagnostic company with an experienced team of passionate and energetic scientists driven to create fast and affordable molecular diagnostic solutions across the globe. We are focused on infectious disease assays in point-of-care and home-based settings. We are looking for an enthusiastic and dedicated Research Associate to implement and execute analytical and scientific experiments to drive Product Development. Demonstrates high degree of organization and planning and the ability to apply scientific principles to plan out and execute experiments involving a variety of laboratory methods. This individual demonstrates technical proficiency, high degree of organization and planning and the ability to apply scientific principles. | 10/27/2022 |
| 5865 | Rakuten Medical San Diego, CA Research Associate I, Upstream BS/MS Exp: >1 years |
Rakuten Medical is currently looking for a highly motivated individual to support cell line and upstream process development activities. This candidate will join Rakuten Medical ’s CMC team focusing on various aspects of preclinical antibody development including transfection and single cell cloning, cell culture process development, late-stage characterization, technology transfer and research material generation. | 10/28/2022 |
| 5866 | Metrics Contract Services Toronto, ON, CA Design Engineer Bachelor’s Degree in Engineering Exp: 1-2 years |
As a Design Engineer on our Product Development Team, you'll collaborate with other engineers and work cross-functionally with our Marketing, Regulatory, Manufacturing, and Quality teams to create and modify designs for surgical instruments for spinal and cranial navigation. This is a great way for you to leverage your engineering degree to gain experience in design feasibility, testing, engineering analysis, design control documentation, and design for manufacturing. You’ll have the opportunity to tackle projects where you can provide solutions to a variety of technical problems related to complex spine products that ultimately impact patients’ lives. | 10/28/2022 |
| 5867 | Metrics Contract Services Carlsbad, CA Quality Engineer Quality Engineer Bachelor’s Degree in Engineering, Science, or related field Exp: 1 year |
The position is responsible for overseeing Quality Engineering activities related to product development and existing product support. The sustaining Quality Engineer approves Quality System documentation, provides technical support to the QC department, participates in improvement projects and CAPAs, and assists in managing external audits. | 10/28/2022 |
| 5868 | Resilience Alachua, FL Specialist, Biomanufacturing (Recent Grad) B.S. (Biology, Microbiology, Chemistry or equivalent) Exp: 0 - 2 years |
This position will assist in production related activities in the cGMP Manufacturing Core according to established procedures at the Medical Counter Measures (MCMs) Advanced Development and Manufacturing Facility in Alachua (Florida). | 10/28/2022 |
| 5869 | Resilience Alameda, CA Research Associate II, Bioanalytical Research Associate II, Bioanalytical BA/BS or MS in Biological Sciences Exp: 1-2 year |
The Research Associate II, Bioanalytical will be responsible for assisting in the development and validation of Ligand-Binding Assays (LBA) for pharmacokinetic (PK), toxicokinetic (TK), biomarkers (PD) and anti-drug antibodies (ADA) and to support sample testing for nonclinical GLP and clinical studies. | 10/28/2022 |
| 5870 | Resilience Alachua, FL Research Associate I-II Research Associate I-II BS degree in microbiology, biology, molecular biology, biochemistry, chemistry. M.S. in same areas. Exp: 0-3 years |
The research associate reports to the Associate Director or Senior Manager of Biologics and performs method development, product and process development, scale up/scale down processing, and performing a wide variety of activities including but not limited to the following responsibilities. | 10/28/2022 |
| 5871 | Resilience Alachua, FL Research Associate I-II Research Associate I-II Research Associate I BS degree in microbiology, biology, molecular biology, biochemistry, chemistry, or related field. M.S. in same areas. Exp: 0-3 years |
The research associate reports to a Senior Scientist of Vaccines and Gene Therapy and performs method development, product and process development, scale up/scale down processing, and performing a wide variety of activities including but not limited to the following responsibilities. | 10/28/2022 |
| 5872 | Resilience East Norriton, PA Manufacturing Technician II Associates/Bachelor’s (science preferred) degree Exp: 1-3 years |
The Technician II, Cell Therapy Manufacturing position is responsible for the hands-on clinical manufacturing of cell therapy product according to current Good Manufacturing Practices (cGMPs) and procedures. The position will work directly with a team of manufacturing technicians, specialists and scientists in Cell Therapy Manufacturing and Process Development and report to the Bioprocess and Cell Therapy Supervisor. | 10/28/2022 |
| 5873 | Resilience East Norriton, PA Manufacturing Technician I Associates/Bachelor’s (science preferred) degree Exp: 0-2 years |
The Technician I, Cell Therapy Manufacturing position is responsible for the hands-on clinical manufacturing of cell therapy product according to current Good Manufacturing Practices (cGMPs) and procedures. The position will work directly with a team of manufacturing technicians, specialists and scientists in Cell Therapy Manufacturing and Process Development and report to the Bioprocess and Cell Therapy Supervisor. | 10/28/2022 |
| 5874 | Rocket Pharmaceuticals Cranbury, NJ Entry Level - Clinical Manufacturing Associate I - Upstream B.A./B.S. in Life Science, Biotechnology, ChemE, or similar relevant field Exp: 0 to 2 years’ |
As a Clinical Manufacturing Associate I, you will be part of a team responsible for the start-up of a cleanroom facility and the cGMP manufacture of viral vector therapies for use in clinical trials. Additional responsibilities include set-up, operation, and cleaning of equipment, equipment, and process monitoring and troubleshooting, receiving materials and supplies from the warehouse, maintaining supply inventories, creating technical documents, and maintaining cleanrooms and equipment in an inspection-ready state. The ideal candidate will also have a strong passion and curiosity for science and gene therapy with the desire to contribute individually and collectively in a dynamic, fast-paced environment. | 10/28/2022 |
| 5875 | Rockland Immunochemicals Pottstown, PA Scientist I - Recombinant Antibodies Bachelor's or Master’s Degree in Molecular Biology, Immunology, Biological sciences or other related degree Exp: 0– 2 Years |
Rockland Immunochemicals is seeking to hire a highly motivated scientist to join our R&D team. This position of Associate Scientist or Scientist I is to participate in all aspects of recombinant antibody discovery including but not limited to primers design, antibody library construction, antibody sequence analysis, cloning, expression and purification, screening. ALL candidates with background in life sciences or related field are encouraged to apply. Training will be provided accordingly. | 10/28/2022 |
| 5876 | SCA Pharma Windsor, CT Microbiology Analyst I -2nd Shift 4 year college degree or equivalent laboratory experience Exp: 0-2 years |
At SCA Pharma, we prepare intravenous medications to be given to patients in hospitals and other healthcare facilities. Our Microbiology lab plays a key role in ensuring the sterily of our facilities and our products, to ensure that only the safest medications leave our facility. As a Microbiology Analyst I, you will be responsible for supporting the Microbiology Department with data processing/entry, Environmental Microbiological testing and Filtration Testing, in addition to daily housekeeping of the laboratory. | 10/28/2022 |
| 5877 | Serotiny South San Francisco, CA Research Associate/Senior Research Associate Degree in molecular biology, cell biology, immunology, biotechnology or related area Exp: Research Associate: BSc. with 0-3 years |
Serotiny is looking for a RA/SRA who is excited to work closely with a team of protein engineers and cell biologists to build out and deploy Serotiny's high-throughput methods to characterize and develop cutting edge therapies. We are looking for a candidate eager to contribute towards the development of a novel platform to generate and characterize CAR T cells for solid tumor indications. | 10/28/2022 |
| 5878 | Sherlock Biosciences Watertown, MA Research Associate BS in Biology, Biochemistry, Bioengineering, or related discipline. Exp: 0-2+ years |
The Research Associate will work closely with our Scientists to develop, conduct, and analyze biochemical and molecular biology experiments to support our CRISPR and Synthetic Biology-based platforms for molecular diagnostics. | 10/28/2022 |
| 5879 | SmartPharm Therapeutics San Diego, CA Research Associate/Senior Research Associate-CAR-T/CAR-NK Bachelor’s degree with relevant experience in Immunology, Molecular Biology or related disciplines. Master’s degree a plus. Exp: 1+ Years |
Sorrento Therapeutics (“Sorrento”) is seeking an experienced Research Associate or Senior Research Associate that has knowledge and hands on experience in gene editing, cell culture, Flow Cytometry and cell-based assays. This position will be responsible for the development and implementation of in vitro studies to support pre-clinical validation of CAR-T/CAR-NK cellular therapies against human cancers. | 10/28/2022 |
| 5880 | SmartPharm Therapeutics San Diego, CA Research Associate Bachelor's Degree in Life Sciences or a related field. Exp: 0-2 years |
Sorrento Therapeutics (“Sorrento”) is seeking a Research Associate who, under close supervision assists in conducting laboratory experiments, maintain laboratory environment, organizing data, and analyzing results. Major tasks include: antibody discovery by phage display, antibody expression and purification, antibody characterization, cell culture and cell based assay | 10/28/2022 |
| 5881 | IQVIA Ithaca, NY Lab Associate Bachelor's Degree Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree required Exp: 6 months |
Responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. | 10/18/2022 |
| 5882 | IQVIA Austin, TX Lab Associate Bachelor's Degree Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree Required Exp: 6 months |
Responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. | 10/18/2022 |
| 5883 | IQVIA Atlanta, GA Lab Associate Bachelor's Degree Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree Exp: 6 months |
Responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. | 10/18/2022 |
| 5884 | IQVIA Durham, NC Associate Scientist, Lab Ops Bachelor's Degree Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree Required Exp: 6 months |
Responsible for performing routine analysis and laboratory testing procedures to obtain data for use in drug development and clinical trials research. | 10/18/2022 |
| 5885 | IQVIA Ithaca, NY Scientist, Lab Operations Bachelor’s Degree, Chemistry and/or Biology preferred Exp: 1 year’s |
The Scientist Core LC/MS (Liquid Chromatography/Mass Spectrometry) employs liquid chromatographic separation techniques and mass spectrometric analysis for data collection. In addition to instrument operation, the Scientist LC/MS is responsible for some associated instrument maintenance, documentation in accordance with SOPs and regulations, and data processing in a manner which meets company quality best practices, objectives, and timelines. | 10/18/2022 |
| 5886 | IQVIA Indianapolis, IN Associate Scientist, ADME Sciences Bachelor’s degree in relevant scientific discipline Exp: 6 months |
Responsible for performing routine analysis and laboratory testing procedures to obtain data from pre-clinical and/or clinical specimens. Provides routine documentation and review of work performed in a timely manner. | 10/18/2022 |
| 5887 | Perrigo Covington, OH QC Chemist II Bachelor of Science degree in a scientific discipline (Chemistry or Food Science preferred, Biology) required Exp: 1-2 years' |
We are currently looking for a highly motivated QC Chemist who will work 3rd shift on a rotating 2/2/3 schedule. This position pays a 10% shift premium. | 10/18/2022 |
| 5888 | Perrigo Georgia, VT Instrument Lab Analyst (2nd Shift) 4-year college degree in Chemistry or a related science is required. Exp: 1-2 years |
Perrigo Nutritionals, located in Georgia, VT, is looking for an Instrument Lab Analyst to join their team. This is a 2nd shift position running Tuesday-Saturday, 4PM-12:30AM. | 10/18/2022 |
| 5889 | Perrigo Allegan, MI Assistant/Associate/Scientist AR&D Bachelor’s OR Master's Degree in Chemistry or Pharmaceutical Sciences Exp: BS: 0-4 years; MS: 0-2 years |
Our focus is on the development of analytical methods for small molecules in support of research and characterization of new and reformulated drug products. Chief techniques include HPLC/UPLC-UV stability-indicating methods with various separation chemistries. Alternate detection methods such as ELSD and RI may also be employed along with introduction of various new analytical technologies as needed. The individual will be responsible for development of assay, impurities, dissolution, water content, and physical characterization methods for liquid and solid oral drug products. There is an expectation of both direct hands-on laboratory work as well as, depending on level of experience, mentoring/training of colleagues. | 10/18/2022 |
| 5890 | MEDTOX Baltimore, MD Research Associate Bachelor’s Degree Exp: 0-2 year |
We are currently seeking an extraordinary, highly motivated individual to join our Research and Development team, with a focus on development and evaluation of emerging technologies for tissue and cell-free DNA liquid biopsy approaches. The successful candidate will assess and optimize laboratory-based diagnostic analyses for research and clinical use following guidelines of regulatory agencies for academic, biotechnology, and pharmaceutical clients. | 10/18/2022 |
| 5891 | Merck Kenilworth, NJ Associate Scientist B.S. or M.S. degree in Chemical/ Biochemical/ Biomedical Engineering, Pharmaceutics, Pharmaceutical Chemistry, Pharmaceutical Sciences, Chemistry, Bio Exp: 0-2 years |
The successful candidate will be a passionate scientist with strong academic fundamentals and a drive to develop new medicines to improve human health. In this role, the individual will be responsible for supporting the formulation development of new biological/ chemical entities as part of a matrix team from initial first in human formulations to commercialization. | 10/18/2022 |
| 5892 | PerkinElmer San Diego, CA Quality Control Associate - Tissue Culture Bachelor’s Degree in Science Exp: 1+ year |
QC Flow Associates focused on cell & tissue culture are highly motivated team members that will primarily be responsible for the preparation of primary cells and the culture of various cell lines, as well as the set up of cell stimulations needed for flow cytometry testing of BioLegend products such as antibodies, protein reagents, buffers for immunology and related research fields. In addition, the employee may perform surface, intracellular, and multicolor testing and analysis. Primary responsibilities include performing experiments (e.g. cell culture, cell preparation and flow cytometry testing); production and analysis of reliable, reportable data; maintaining accurate documentation, utilization of internal company databases for product filing and retrieval; following company SOPs and ISO requirements. | 10/18/2022 |
| 5893 | PerkinElmer San Diego, CA Biochemist - Immunoassay - ELISA BS/BA in Biology, Chemistry, or other life science-related field. Exp: 1 year or more |
BioLegend is seeking a highly motivated Manufacturing Associate to join the Biomarker Immunoassay team in San Diego. The Manufacturing Associate will work closely with team members to ensure the timely manufacturing of high quality immunoassay products under ISO13485 standards. The Manufacturing Associate will be working closely with others in the team to ensure timely manufacturing of high-quality immunoassay products under ISO13485 standards. This role will be responsible for all aspects of product manufacturing including planning/scheduling, making and testing immunoassay components and kits, troubleshooting issues associated with product quality, and documenting and reviewing production batch records to ensure accuracy and completeness. Additional responsibilities include working with the Product Development team to ensure proper transfer of new products from Product Development to Manufacturing, filling daily immunoassay kit orders from inventoried components, and making and testing custom products in a timely manner. | 10/19/2022 |
| 5894 | PerkinElmer San Diego, CA Biochemist - Immunoassay - ELISA BS/BA in Biology, Chemistry, or other life science-related field. Exp: 1 year or more |
BioLegend is seeking a highly motivated Manufacturing Associate to join the Biomarker Immunoassay team in San Diego. The Manufacturing Associate will work closely with team members to ensure the timely manufacturing of high quality immunoassay products under ISO13485 standards. The Manufacturing Associate will be working closely with others in the team to ensure timely manufacturing of high-quality immunoassay products under ISO13485 standards. This role will be responsible for all aspects of product manufacturing including planning/scheduling, making and testing immunoassay components and kits, troubleshooting issues associated with product quality, and documenting and reviewing production batch records to ensure accuracy and completeness. Additional responsibilities include working with the Product Development team to ensure proper transfer of new products from Product Development to Manufacturing, filling daily immunoassay kit orders from inventoried components, and making and testing custom products in a timely manner. | 10/19/2022 |
| 5895 | PerkinElmer San Diego, CA Biochemist - Biomarker and Immunoassay Group (LEGENDplex™) Biochemist - Biomarker and Immunoassay Group (LEGENDplex™) Biochemist - Biomarker and Immun Bachelor’s Degree in a Biology, Chemistry, or other related field Exp: 0-2 years |
The Manufacturing Associate for the LEGENDplex™ Group will be responsible for all aspects of product manufacturing, including planning, making and testing immunoassay components and kits, trouble-shooting issues associated with product quality, and documenting and reviewing production batch records to ensure accuracy and completeness. Additional responsibilities include working with the Product Development team to ensure proper transfer of new products from the Product Development Group to Manufacturing. | 10/19/2022 |
| 5896 | PerkinElmer San Diego, CA Biochemist - GMP Bachelor’s degree Exp: 1-year |
This position is responsible for different stages of manufacturing of various BioLegend’s regulated product produced in our US FDA registered cGMP manufacturing facility. The candidate will be responsible for formulating, filling, capping, labeling, completing batch records, putting away finished good inventory (FGI), data entry, equipment maintenance and supply inspections & storage. Other responsibilities include purification of monoclonal antibodies derived from tissue culture material through an AKTA system. As well as the conjugation of purified antibody through the AKTA system. Buffer preparation and inspection of incoming buffers into the GMP suite will also be performed. Another part of the job responsibility includes preparing product/project related documentation and maintaining the device history records for all the regulated products. Working closely with product development on new products in order to establish a smooth transition into manufacturing will also be required. The desired candidate must be a team-player who is organized and has strong verbal and written communication skills and is able to work in a very fast paced environment. Great attention to detail is also a skill that will allow the candidate to be successful. The candidate must also be able to work independently and meet deadlines. | 10/19/2022 |
| 5897 | Sanofi Framingham, MA Quality Control Analyst I Bachelor’s Degree Exp: 0-2 Years |
Shift Schedule: Sunday-Wednesday shift, 12:00 pm - 10:30 pm. This position is responsible for performing routine and complex testing of in-process samples and final products in accordance with SOPs and relevant procedures for method development, qualification, validation, method transfer, product release, stability, and process validation and investigations. | 10/20/2022 |
| 5898 | Sanofi Chattanooga, TN Quality Control Lab Chemist I Bachelor’s degree in Chemistry or related field. Exp: Zero to three years |
Perform testing of ingredients as required to support production requirements. Assure that testing is properly documented and that the ingredient is dispositioned in accordance with the results of the test and the appropriate standard operating procedures. Perform routine laboratory testing for bulk and finished product to support production or shipping requirements. Assure that testing is properly documented and that the bulk or finished product is dispositioned in accordance with the results of the test and the appropriate standard operating procedures. Perform stability testing in support of the room temperature stability program. Assure that stability testing is completed in a timely manner and within the designated time frame. Complete stability testing documentation as appropriate. Knowledge of and ability to use lab instruments including but not limited to: UV-VIS, HPLC, GC, ICP, AA, and FTIR. | 10/20/2022 |
| 5899 | Sanofi Framingham, MA Manufacturing Technician Bachelor’s degree Exp: 1-2 years |
**12 hour rotating SHIFT** This position is responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMPs. | 10/20/2022 |
| 5900 | Sanofi Framingham, MA Senior Manufacturing Technician Bachelor’s degree Exp: no prior experience |
**12-hour rotating day shift position including rotating holidays and weekends and overtime as per business needs** **Great promotion opportunity to build leadership skills** **Cell Experience preferred** Position in a cGMP biologics facility which includes small scale and large scale upstream operations. Initial job responsibilities will include performing a diverse range of manufacturing related activities. The Manufacturing Associate will be responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMPs. | 10/20/2022 |
| 5901 | Sanofi Swiftwater, PA Production Technician - Vaccine Bachelors degree in Life Sciences or other relevant field of study. Exp: no prior manufacturing experience necessary |
This a third shift position. Must be able to work weekends and holidays as needed. Performs production in accordance with volume fluctuation, business need and effective procedures. Responsible for Manufacturing activities in assigned area. Identifies all production issues and relays them to the leadership team. Works to prepare assigned areas for the oncoming shifts. Completes tasks and corresponding documentation as required by cGMP. Position includes responsibilities to hand pack, operate machinery, change over duties, and clean-up functions, to assure a smooth transition between product lines. Works with Senior Technicians and Managers to ensure a smooth operation. Works to become trained in all assigned training modules. Trains and orients new team members (at any level) as assigned. Follows all procedures put into effect to ensure your safety as well as the safety of others. | 10/20/2022 |
| 5902 | Sanofi Swiftwater, PA Production Technician LL2 - Vaccine Bachelors Exp: 0+ yrs |
Performs production in accordance with volume fluctuation, business need, and effective procedures. Responsible for Manufacturing activities in assigned area. Identifies all production issues and relays them to the leadership team. Works to prepare assigned areas for the oncoming shifts. Completes tasks and corresponding documentation as required by cGMP. Position includes responsibilities to hand pack, operate machinery, change over duties, and clean-up functions, to assure a smooth transition between product lines. Works with Senior Technicians and Managers to ensure a smooth operation. Works to become trained in all assigned training modules. | 10/20/2022 |
| 5903 | Invitrogen Carlsbad, CA Antibodies QC Scientist I Bachelor of Science degree in Biology, Cell Biology, or life science related field Exp: 0-3 years |
As Manufacturing Scientist I, this individual will assure that work is performed in accordance with production schedules, perform hands-on manufacturing tasks and work in a fast-paced manufacturing environment, conduct multiple production runs at one time, and be well organized. | 10/20/2022 |
| 5904 | Invitrogen Rockville, MD Lab Technician I BS in a Biological Science Exp: 1 yr. |
The Laboratory Technician will assist in manual and automated laboratory processing of biological materials, including aliquoting and sample preparation. Tuesday-Saturday shift. | 10/20/2022 |
| 5905 | Invitrogen West Hills, CA Scientist I, Technical Operations Bachelor’s degree in Biology, Chemistry, or other similar Life Science field required Exp: 0-2 years |
The Scientist I position requires the ability to write equipment validation protocols, execute validations, and write reports for equipment. Assessing new materials requires the capability to perform risk-based comparisons of new materials to material specification documents. | 10/20/2022 |
| 5906 | Invitrogen West Hills, CA Scientist I, Manufacturing Sciences Bachelor’s degree in Biological Sciences, Biochemistry, Chemistry, Molecular Biology or related field. Exp: 0+ years |
The Scientist I, Manufacturing Sciences is responsible to lead, perform, and prioritize assigned projects related to development, improvement, production, and QC of antibody detection reagents with supervision. | 10/20/2022 |
| 5907 | Invitrogen St. Louis, MO Scientist I, QC Microbiology Bachelor’s degree required in a scientific field, preferably a Microbiology or Biology. Exp: 0 - 2 |
Provide routine analyses in microbiology by following standard practices. Perform microbiological testing of in-process samples, raw materials, buffers, media, etc. per compendial methods. Support internal development and/or manufacturing operations. Make detailed observations and reviews, documents, and communicate test results. | 10/20/2022 |
| 5908 | Invitrogen Carlsbad, CA Scientist I, Process Development Bachelors in Life Sciences, Engineering, Biochemistry, Biology or related field Exp: 1+ years |
In this role you will work alongside clients to design, develop and optimize processes that produce Plasmids for CGT and/or mRNA vaccines These Plasmids are used to treat or cure patients of life threating diseases. | 10/20/2022 |
| 5909 | Jordi Labs Mansfield, MA Chemist Master’s degree in chemistry or other closely related field. Exp: one year |
Job duties: 1) Prepare technical reports 2) Interpret gas chromatograph mass spectrometry (GCMS) and liquid chromatograph mass spectrometry (LCMS) results with a high level of proficiency 3) Interpret chromatographic data including high performance liquid chromatography (HPLC), gas chromatography (GC), and gel permeation chromatography (GPC) results 4) Combine results from multiple techniques to identify unknown chemical compounds 5) Quantify chemical components using HPLC and GC results 6) Work with a team of scientists to design and implement analytical strategies 7) Perform or oversee complex analytical strategies with an emphasis of MS and chromatography 8) Review technical reports written by other scientists | 10/20/2022 |
| 5910 | Krystal Biotech Pittsburgh, PA Research Associate, Analytical Sciences and Clinical Testing Services Bachelor’s degree (Biology, Biochemistry, Chemistry, or related science) Exp: 1-3+ years |
Krystal Biotech, Inc is seeking a highly motivated a Research Associate, Analytical Sciences and Clinical Testing Services to perform high quality analytical testing in support of Krystal’s process development and product development efforts. This position will be laboratory based. | 10/20/2022 |
| 5911 | Manifold Bio Boston, MA Research Associate / Senior Research Associate, In Vivo PharmacologyResearch Associate / Senior Research Associate, In Vivo Pharmacology Bachelors or Masters Exp: 1-2+ years |
We are seeking a highly-motivated In Vivo Pharmacology Research Associate / Senior Research Associate who thrives in a fast-paced and creative environment to push the capabilities of our multiplexed in vivo drug discovery platform. Together with senior researchers, you will play a critical role in executing in vivo studies to support internal research projects. This is a hands-on role and you should have extensive experience in multiple aspects of in vivo pharmacology including dosing, pharmacokinetic sampling, and necropsy, among others. The ideal candidate must be able to work effectively both in a collaborative setting and Independently. | 10/20/2022 |
| 5912 | Masy Bioservices St. Louis, MO Associate Scientist I, Microbiology Bachelor’s degree Biology, Microbiology or related field. Exp: 0-2 years |
The Associate Scientist, Microbiology is accountable for driving results in a fast-paced environment by accurately and efficiently performing sample analysis, monitoring microbial cultures and identifying microbiological contaminants and pathogens using a variety of identification methods. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 10/20/2022 |
| 5913 | Masy Bioservices Charleston, SC Associate Scientist I, Microbiology - 3rd Shift Bachelor’s degree in Chemistry, Biology, Microbiology or a related field. Exp: 0 – 2 + years |
The Associate Scientist I is accountable for driving results in a fast-paced environment. The position is responsible for performing monitoring of the pharmaceutical manufacturing environment and utilites in complaince with cGMP and internal SOPs. The incumbent will provide support to manufacturing and laboratory operations. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. | 10/20/2022 |
| 5914 | Med Institute Pittsburgh, PA Quality Control Associate I Undergraduate degree any Life Sciences, Engineering field, Microbiology, or Molecular Biology Exp: 1-3 years' |
The Quality Control Associate I at Cook MyoSite will aid in the development and maintenance of methods for sampling, testing, evaluating, and approving testing results for products and materials. | 10/20/2022 |
| 5915 | Mekonos Berkeley, CA Research Associate, Chemistry B.S or M.S in Chemistry, Chemical Engineering, Material Science, Biochemistry or a related discipline Exp: 1-3 years |
Further the development of our patented delivery chemistry Plan and execute research operations Assist with lab management tasks (procurement, inventory, equipment maintenance, etc.) Demonstrate high scientific integrity and reporting standards Promote a positive and exciting work environment | 10/20/2022 |
| 5916 | Minnetronix Medical St. Paul, MN Design Quality Engineer Bachelor’s Degree/Technical Degree in Engineering or equivalent experience Exp: 0-5 years’ |
Design Quality Assurance Engineers work with design teams to ensure that electronic and software subsystems incorporated into medical devices are designed in accordance with product requirements and the devices meet their intended use. They develop and perform verification and validation activities on medical devices and medical device systems. Verification testing may involve GUI testing, black-box system testing, environmental testing, requirements based functional testing and low-level hardware testing and fault simulation. Design QA Engineers drive quality in all project deliverables and ensure that development teams follow processes that are effective and compliant to Standard Operating Procedures. They work with both the customer and internal team members to drive successful outcomes and long-term value for both the customer and Minnetronix. Design QA Engineers may work under the direction/supervision of more senior Design QA staff members to ensure resolution of technical issues and knowledge transfer. | 10/21/2022 |
| 5917 | Minnetronix Medical St. Paul, MN Manufacturing Engineer I Bachelor’s degree in an engineering, technical or scientific disciple. Exp: 0-3 Yrs |
Manufacturing Engineer I will work cross functionally to manage the production build of complex electro-mechanical medical devices. A Manufacturing Engineer I can be responsible for the production build of multiple product lines. Their responsibilities include: production documentation, issue tracking and resolution, and continuous improvement. | 10/21/2022 |
| 5918 | Myriad-RBM Austin, TX Lab Associate Bachelor's Degree Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree Required Exp: 6 months |
Responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. | 10/21/2022 |
| 5919 | NAMSA Irvine, CA Associate Microbiologist Bachelor degree Exp: one year |
Independently perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs, and according to applicable work instructions. • Prepare or participate in the preparation of test specifications in conjunction with the requirements of the applicable standards and/or client instructions. • May have direct client contact as needed. | 10/21/2022 |
| 5920 | NAMSA Northwood, OH Microbiology Technologist Bachelor degree Exp: no experience |
May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. • Accurately collects and records raw data in logbooks and on worksheets. • May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. • May be required to perform personal gowning environmental testing, and submit organisms from gowning, environmental and sterility test positives for identification and inclusion in monthly trending data, as required for specific testing as applicable. • May be required to operate autoclave, depyrogenation oven or other specified laboratory equipment. • May perform Kinetic-Chromogenic LAL testing. • May perform Environmental Monitoring, clean and disinfect cleanroom suites. • Other duties as assigned | 10/21/2022 |
| 5921 | Frontida BioPharm Philadelphia, PA ASSOCIATE ANALYTICAL SCIENTIST Master’s Degree Exp: 1+ years |
The Analytical Scientist II reports to the Associate Director of Analytical Research and Development and is based at our Philadelphia location. This is a laboratory-based position and the Scientist will be responsible to support formulation development by performing method development, validation, writing protocols and reports, conducting chemical and physical testing activities for both ANDA and NDA projects. | 10/11/2022 |
| 5922 | Frontida BioPharm Vandalia, OH QC ANALYST Bachelor degree in Chemistry or related field Exp: 0 to 3 years |
The essential job function is to perform physical and chemical testing of intermediate and finished products according to written procedures. | 10/11/2022 |
| 5923 | Frontida BioPharm Vandalia, OH QC ANALYST (NIGHT SHIFT) Bachelor degree in Chemistry or related field Exp: 0 to 3 years |
The essential job function is to perform physical and chemical testing of intermediate and finished products according to written procedures. | 10/11/2022 |
| 5924 | Frontier Medicine South San Francisco, CA Compound and Sample Associate I B.S. or M.S. in Chemistry, Chemical Engineering, Biology or related discipline required Exp: 0-1 year |
Frontier Medicines is seeking a highly motivated individual for a newly created Compound and Sample Associate I. The successful candidate will be accountable for the storage, retrieval, and distribution of compounds for biological assays as well as chemical building blocks for compound synthesis and QC. The position is located in South San Francisco, CA. | 10/11/2022 |
| 5925 | Frontier Medicine South San Francisco, CA Research Associate, Protein Sciences BS or MS in Biochemistry, Biological Sciences, or a related field Exp: 0-2 years |
We are seeking highly motivated research associates to join our group in South San Francisco, CA. This is an exciting opportunity for experienced and passionate associates or recent graduates to apply and expand their skills in protein sciences and contribute to the discovery of innovative therapies. The successful applicants will carry out experiments in protein expression, purification, and characterization to support biochemical assays and structure determination. Working closely with an experienced team of interdisciplinary scientists, the candidates will have regular opportunities to present findings to the Protein Sciences team. The ideal associates should have a strong desire to learn new techniques and incorporate new methodologies into their work, as well as be detail-oriented, self-motivated, well organized, and enjoy working and learning in a dynamic team environment. | 10/11/2022 |
| 5926 | Fujifilm Diosynth Mesa, AZ Process Technology Engineer BS Degree Engineering (Chemical, Mechanical or Materials Science preferred). Exp: 0 to 2 years |
The Process Technology Engineer will work with the Process Technology Group (PTG) to operate process scaling equipment, collect ultra-high purity samples from both pilot and full scale operating equipment to issue summary reports as directed by PTG’s senior engineering staff. | 10/11/2022 |
| 5927 | Fujifilm Diosynth College Station, TX Process Sciences - Associate Engineer - Material Transfer Bachelor’s/ Master’s Degree Degree in a science related field Exp: 1 year |
The Material Transfer Associate is responsible for compiling, organizing and reviewing documents that summarize safety testing results and/or describe safety characteristics of select incoming materials. They are also responsible for performing the material entry evaluation, identify gaps and perform risk analysis when needed to complete the material induction process. In addition, the Material Transfer Associate will be working with internal and external stakeholders to complete the transfer of materials from the client(s) to FDB (Fujifilm Diosynth Biotechnologies) for supporting process development work and cGMP manufacturing activities by monitoring inventory and tracking incoming materials, especially biological materials. | 10/11/2022 |
| 5928 | Fujifilm Diosynth College Station, TX QC Cell Biology Analyst II Master’s degree preferably in Biology or Biochemistry Exp: one (1) year |
The Cell Biology Analyst II will be responsible for participating in the Technology Transfer of established methods into the FujiFilm Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory. | 10/11/2022 |
| 5929 | Glypmse Cambridge, MA Research Associate/Sr. Research Associate, Chemistry high throughput screening BS or MS equivalent degree in chemistry, biochemistry, biology or relevant discipline Exp: 1-3 years |
Our Screening and Automation group is seeking a motivated Research Associate who will contribute to the development of novel diagnostics in our Chemistry platform. This person will perform work at the intersection of Chemistry, Biology and Computational Science, participating in experimental design and execution, generating data, and collaborating on analyses. The individual we hire will have the opportunity to lead screening campaigns, execute on established workflows, optimize and develop new assays, and help build out new tools and functionalities. | 10/11/2022 |
| 5930 | HemoSonics Raleigh/Durham/Chapel Hill, NC Associate Quality Engineer BA/BS degree in science, engineering or related technical field Exp: 1 - 4 years’ |
HemoSonics, LLC is seeking an Associate Quality Engineer for our Quality Assurance team. This position is responsible for providing quality engineering support to the management and maintenance of all Quality Systems elements to meet the company’s business needs, developing company best practices, standards, continuous improvement and ensuring compliance with regulatory requirements and standards. The Associate Quality Engineer works cross functionally with Operations, Supply Chain Management, R&D and internal quality groups to provide guidance on GMP and best practices. | 10/12/2022 |
| 5931 | HistoTox Labs Gaithersburg, MD Animal Study Technician I B.S. or B.A. degree in Biology, Life sciences, Chemistry or Science field Exp: 0+ years |
Learns how to review study protocol and ensure study tasks and data for pre-clinical research studies are conducted in accordance with established protocols, SOPs, GLPs, and other pertinent regulatory requirements. Learns how to generate study forms and worksheets. Receives extensive training in various technical procedures including dose administration, sample collection, handling and restraint of multiple species. Learns to perform and document observations on study animals. Learns to record observations and collect other relevant data via data capture systems and/or hand-generated forms in accordance with GLPs, SOPs, and protocol. | 10/13/2022 |
| 5932 | HistoTox Labs Rockville, MD Associate Scientist - Biotherapeutics BSc or MSc in Immunology, molecular biology, bioanalytical chemistry, drug metabolism, pharmacokinetics, or related science Exp: 1-3 years |
The associate scientists should have knowledge and experience in ligand binding assay techniques, e.g., ELISA, MSD, Luminex, cell-based assays for PK and Immunogenicity determinations, or knowledge of PCR, DNA, RNA analysis, as well as flow cytometry. Due to the different techniques involved, some associate scientists would need essential experience in PCR, DNA, RNA, and flow cytometry analysis with a working knowledge of ligand binding assay techniques, e.g., ELISA (HELISA, etc.), MSD, Luminex, cell-based assays for PK and Immunogenicity determinations and LC-MS/MS. Depending on their experience and capabilities they will be placed in the different sections. The associate scientists of the Biotherapeutics laboratory will perform analysis of samples generated in the GLP/GCLP laboratory for preclinical samples according to the applicable FDA/EMA Guidelines. The associate scientists will thrive in a collaborative and welcoming environment that values a culture of empowerment, transparency, innovation, agility, professional growth, and credibility providing them the opportunity for promotion to scientists. | 10/13/2022 |
| 5933 | HistoTox Labs Rockville, MD Associate Scientist I (In Vitro Cytogenetics) Bachelor’s degree in a scientific discipline (i.e., Biology, Chemistry, Biochemistry, etc.) Exp: 1+ years |
Perform a wide variety of in vitro assays or tests required to characterize product or material safety Maintain sterile and good cell/tissue culture techniques Prepare study reagents in accordance with SOPs and study instructions Use and maintain scientific equipment, instrumentation and computer systems Conduct pre-designed assays using basic laboratory techniques and skills Make scientific observations, maintain detailed data books/documentation and ensure all documentation fulfills generally accepted professional/industry standards and GLP regulations Perform peer review of data and lab support records | 10/13/2022 |
| 5934 | HistoTox Labs Raleigh, NC Research Assistant A.S. or B.S. in biology or related field Exp: 0-3 years |
We are expanding in our Genetic Toxicology team in our Research Triangle Park location. Our group is performing regulated toxicology studies in laboratory rodents for commercial and governmental clients. Responsibilities The Genetic Toxicology Group conducts standard and custom genetic toxicology testing and applied research supporting preclinical studies for both federal and commercial clients. | 10/13/2022 |
| 5935 | HistoTox Labs West Lafayette, IN Bio Analyst I B.S. in chemistry or biology Exp: one year |
Conducts sample analysis with data interpretation and basic troubleshooting. Conducts method development and method validation experiments. Assists with general housekeeping and assist other departmental personnel as necessary. | 10/13/2022 |
| 5936 | IFyber Ithaca, NY Laboratory Technician a BS degree Exp: 1 year (more preferred) |
The Laboratory Technician will execute on experimental plans at the interface between chemistry, biology, and materials science and support a variety of programs that will require experience and/or the ability to follow detailed protocols, learn and execute bench skills, and adhere to applicable regulatory requirements. | 10/13/2022 |
| 5937 | IGM Biosciences Doylestown, PA Research Associate II / Research Associate III MS or equivalent in Biology, Immunology, or another related science degree Exp: RAII: MS with 0-2 years |
We are looking for a Research Associate II/III with a background in in vitro immunology assays and the development of biologics to join our growing and friendly team during this exciting time in our expansion. The successful candidate will play an integral role in developing novel autoimmune and inflammation therapeutics pre-clinical development. You will perform in vitro studies, standard immuno-assays, problem solve and constantly improve work practices and work productively as part of a team contributing to advancing innovative applications of the IgM platform for autoimmune and inflammatory disease. | 10/13/2022 |
| 5938 | IGM Biosciences Doylestown, PA Research Associate / Senior Research Associate, Drug Product Degree in Biochemistry, Chemistry, Biology, or related background. Exp: MS with 0 - 2 years |
We are hiring a Research Associate to join our rapidly growing Drug Product team in support of IGM program development. In this position you will be responsible for executing scientific research and development projects in collaboration with colleagues across business units and programs to support end-to-end Research & Development and Company goals. You will execute studies to develop frozen, liquid, dried, and novel Drug Product and develop devices to enable pre-IND and post-IND clinical requirements. You will engage with all partner groups including upstream pre-clinical discovery and Drug Substance purification through downstream manufacturing, clinical supply, operations, analytical, and regulatory colleagues internally. | 10/13/2022 |
| 5939 | IGM Biosciences Mountain View, CA Research Associate II / III, Cell Line Development BS or MS in Cell Biology, Biochemistry, or related scientific discipline. Exp: 1 – 3 years |
IGM Biosciences is hiring a Research Associate in our Cell Line Development group to join our rapidly growing team. In this position you will support the development of novel antibody products by helping to create cell lines producing these therapeutic antibodies. You will work on cell pool generation, single cell cloning, maintain and expand cells, cell banking, cell line characterization, and execute antibody production runs. | 10/13/2022 |
| 5940 | InBios International Seattle, WA Manufacturing Associate I- ELISA Bachelor’s degree with emphasis on life science Exp: 1-year |
We would like to see your resume if you have received a degree with an emphasis on life sciences. If you have work experience in a GMP/ISO 13485 manufacturing facility and/or you have experience with PCR test-kit manufacturing please be sure to include that information on your resume or in a cover letter. If you would like to be part of a team responsible for the production of large-scale ELISA diagnostic test components in a BSL-2 laboratory, and you enjoy a busy workday under general supervision with daily goals working alongside a dedicated team that consistently meets deadlines and delivers products that meet high quality standards, then we encourage you to apply for this position. | 10/13/2022 |
| 5941 | InBios International Seattle, WA Manufacturing Associate I- Rapid Spray Bachelor’s degree in life sciences or a similar field Exp: 1 year |
We are searching for entry-level candidates to join our Biotech manufacturing team to support efforts in producing EUA-approved Covid-19 antigen tests and other Inbios products. This position is ideal for someone who wants to start out working in a biotech laboratory/manufacturing environment, learn industry standard good manufacturing practices (GMP), is ready to learn new skills and procedures and is comfortable working with machines and with your hands. We would like to see your resume if you have general industrial or academic laboratory experience and a willingness to learn more lab skills. This position provides opportunity for working with a team and independently on a variety of tasks including preparing buffers, running semi-automated machines, and producing large-scale lateral flow diagnostic test components. If you are seeking an entry-level position with short-term and long-term opportunities for experience and growth at the forefront of medical diagnostic biotechnology this is a great opportunity for you. | 10/13/2022 |
| 5942 | InBios International Seattle, WA Quality Assurance Associate II MS Exp: 1+ years |
We are seeking a mindful and diligent individual with a warm and welcoming attitude who has excellent organizational and communication skills and a keen eye for detail. If you enjoy analytical work, leading and collaborating on projects, a variety of responsibilities, and being part of a reliable and dedicated Quality Assurance team, then we encourage you to apply for this position. | 10/13/2022 |
| 5943 | InBios International Seattle, WA Quality Control Assistant - Biotech BS in Chemistry, Biology, Bioengineering, or other relevant discipline. Exp: 0 – 1 year |
You have a degree in chemistry, biology, bioengineering or related life science field of study and are looking for an entry level QC position and an opportunity to learn and grow your skills and career. You thrive in a busy and structured work environment working with a team of Quality Control Associates under the supervision of the Quality Control Manager. You are thorough and able to see and report details and variances as well as able to follow and adhere to established procedures and protocols. You are a reliable worker who is comfortable working and contributing to team demands and goals. | 10/13/2022 |
| 5944 | InBios International Seattle, WA Quality Control Associate I BS or MS in Bioengineering, Chemistry, Biology or other relevant discipline. Exp: 1 year |
You are looking for a new job working with a dedicated and reliable team of quality control professionals. You are a meticulous individual who thrives in an environment with demanding attention to detail; and you take pride in meeting deadlines, using your critical thinking skills, and working with your team and other teams to ensure top quality products are delivered. You have a warm and welcoming attitude and outlook as you approach each workday. If this describes you and the kind of team and work environment you are seeking, we encourage you to apply. | 10/13/2022 |
| 5945 | Instil Bio Thousand Oaks, CA Research Associate, Cell Biology MS Degree Exp: 1+ years |
We are seeking a highly motivated individual to join the research team to participate in Instil Bio’s late-stage efforts and play a pivotal role in advancing key TIL engineering programs to clinical stage. The successful candidate will be part of a research team focused on advancing current programs to IND. In this role, the candidate will initially be directly reporting to Director of Late-stage Research. | 10/13/2022 |
| 5946 | IntelliSyn R&D Waltham, MA Research Associate BS or MS in Chemistry or related subject Exp: 6 months-2 years |
X-Chem is seeking a candidate for the position of Research Associate, Library Synthesis in its Discovery Chemistry group. X-Chem is a drug discovery company that uses DNA-encoded library (DEL) technology to discover leads for therapeutic targets. As a world leader in DEL technology, X-Chem collaborates with numerous pharmaceutical and biotechnology companies, resulting in over 70 licensed programs to date. | 10/13/2022 |
| 5947 | Pace Analytical Maplewood, MN Lab Analyst - Microbiology BS degree in Biological science or related field Exp: 1-3 years |
This position will actively support food safety and quality assurance through the use, and validation of, pathogen detection products. The analyst will prepare and evaluate samples using aseptic technique to ensure products meet specifications. The products being monitored are crucial to maintaining consumer safe food supply chains. Work is performed as part of a team in a collaborative environment. | 10/13/2022 |
| 5948 | Invicro San Diego, CA Associate Scientist, Radiochemistry M.S. or B.S. Exp: 1-3 years’ |
Invicro is seeking a full-time Associate Scientist to focus on Radiochemistry. All levels of chemistry trained individuals are encouraged to apply. This role will be focused on radioisotope labeling of various small and large molecules, along with using analytical techniques to evaluate the labeled products. The radiolabeled molecules will be provided to imaging lab teammates who will carry out PET and SPECT imaging studies on rodents. Radiochemistry experience is desirable, but not required, and complete training will be provided by an experienced radiochemist. Though the radiochemistry experience is not mandatory, the ideal candidate should have knowledge in organic synthesis, product purification, and analytical chemistry. The candidate should have a strong desire to learn radiochemistry and operation of analytical equipment (full training will be provided). The candidate should be able to work independently with remote support where necessary. The role requires radiation safety training before learning radiochemistry and managing the labeling chemistry for PET and SPECT imaging projects. | 10/13/2022 |
| 5949 | Invicro Aliso Viejo, CA Laboratory Assistant, Pathology Bachelor’s degree in a relevant biological science. Exp: 1-2 years’ |
Make an impact at a dynamic and growing company! Invicro seeks a Laboratory Assistant for Advanced Pathology Services to support for all routine Histology and IHC work pertaining to delivery of CAP/CLIA and GLP-like oriented lab services offered to external partners, including BioPharma, Academia, and Oncology Research Centers. Our laboratory performs high complexity immunohistochemistry and other advanced tissue analysis approaches unique to Invicro. This individual should enjoy challenging and analytical work and be motivated by the idea that together we can accomplish great things and make a positive contribution to society through our mission. | 10/13/2022 |
| 5950 | Invicro San Diego, CA Associate Scientist, In vivo Imaging and Pharmacology BS in bioengineering, biomedical engineering, medical physics, radiologic sciences, biology, pharmacology, or other engineering degree Exp: 1-3 years |
Invicro is currently looking for an Associate Scientist to join its San Diego based lab. The candidate will execute in vivo, small animal medical imaging studies and related in vivo pharmacology procedures, including nuclear medicine (PET/SPECT), computed tomography (CT), and magnetic resonance imaging (MRI). The candidate will join a team in our multi-modal imaging laboratory and aid in the development of novel therapeutics and diagnostics. This position will provide an opportunity for rapid technical growth and exposure to cutting-edge pharmaceutical industry research projects. The successful candidate will join a close, dynamic, expanding, diverse and highly performing team. | 10/13/2022 |
| 5951 | InVivoScribe San Diego, CA Manufacturing Associate I B.S. Degree in a scientific discipline, preferred. Exp: 1+ years |
We are looking to add a Manufacturing Associate I to our team for all aspects of production, including the production of master mixes and controls. You will contribute to the drafting and review of new documents, including SOPs, Batch Records and Purchasing Specifications. | 10/13/2022 |
| 5952 | Vigene Biosciences Northridge, CA Research Associate I Bachelor’s degree in Biological Sciences required. Exp: 1 year |
This position is responsible for the evaluation of human blood products for manual or automated cell isolations, product manufacturer, and cell culture. Perform QC testing and create a certificate of analysis (COA) for products manufactured. Record isolation details on a processing worksheet using good documentation practices. Operate flow cytometer and basic lab equipment. | 10/13/2022 |
| 5953 | Vigene Biosciences Memphis, TN QC Flow Analyst 1 BS or higher degree in the biological sciences or related field Exp: 1-2 years |
Charles River Laboratory Biologics is currently seeking an Analyst 1 to perform flow cytometry for our Quality Control Department. The successful candidate will be responsible for performing routine quality control product and raw material release testing utilizing multi-color flow cytometry as well as various biochemistry, molecular biology, and general laboratory techniques according to GMP. Additionally, the analyst will assist QC Scientists with technology transfer of new client assays by Co-authoring SOPs or other required documentation. The position requires the utmost attention to detail, very strong organizational skills, computer proficiency, and a basic understanding of laboratory instrumentation. In addition, effective communication skills and the ability to function in a fast-paced, highly technical environment with minimal supervision are essential for success. | 10/13/2022 |
| 5954 | Vigene Biosciences Memphis, TN Manufacturing Associate I (EG) - 4 - 10 Hour Shifts Available AS or BS in a scientific field strongly preferred. Exp: Zero to 1 year |
We are seeking a Manufacturing Associate for our Cell Therapy Manufacturing Facility located in Memphis, TN. The Manufacturing Associate I is responsible for performing various manufacturing activities related to the start- up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to work night, weekends, and holidays. Must be able to meet physical requirements established in this job description. | 10/13/2022 |
| 5955 | Vigene Biosciences Memphis, TN Quality Ops Specialist I bachelor’s degree in scientific field. Exp: Zero (0) to one (1) year |
We are seeking a Quality Ops Specialist I for our Cell Therapy Manufacturing Facility located in Memphis, TN. | 10/13/2022 |
| 5956 | Vigene Biosciences Memphis, TN Quality Control - Analyst Raw Materials A.A. or B.S. degree in Chemistry, Biochemistry, Biology or related discipline is required. Exp: 0-2 years |
Charles River Biologics in Memphis is seeking applicants for the QC Raw Material Analyst I position. As a key member of our Quality Control department, the Analyst is responsible for the day to day activities covering the inspection, sampling and testing of incoming raw materials. The analyst will report into the Manager and/or Supervisor of the QC Raw Material Department. | 10/13/2022 |
| 5957 | Align Technology San Jose, CA Associate Scientist Bachelors in Chemistry or polymer chemistry or related fiele Exp: 0-2 years |
We are looking for an innovative candidate to be a key contributor as a Associate Scientist in our San Jose, CA location. As a key member of the R&D Materials Engineering team, you will be responsible for supporting on the new product development as well as improving Align's existing products. The ideal candidate will have a background in chemistry and 3D printing resin development. | 10/13/2022 |
| 5958 | Charles River Laboratories Spencerville, OH Research Technician Assistant (Entry Level) Associates or BA/BS in a life science field preferred. Exp: 0-6 months |
A Research Technician Assistant is responsible for: collecting and recording data in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Hourly Rates $18-$19/hr. $1000 Sign on Bonus. 3 weeks vacation and additional sick time. | 10/14/2022 |
| 5959 | Charles River Laboratories Spencerville, OH Research Technician Assistant (entry level) Associates or BA/BS in a life science field preferred. Exp: 0-6 months |
A Research Technician Assistant is responsible for: collecting and recording data in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Hourly Rates $18-$19/hr. $1000 Sign on Bonus. 3 weeks vacation and additional sick time. | 10/14/2022 |
| 5960 | Charles River Laboratories S. San Francisco, CA Research Associate I BS in the biological sciences or relevant area required. Exp: 0-3 years |
Explora BioLabs, an entity of Charles River, is seeking a Research Associate I located in San Francisco, CA. In this role, the incumbent will perform a variety of animal procedures to support company and client research projects (e.g., set up the study forms, set up the procedure rooms, label and ship samples, etc.). To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. | 10/14/2022 |
| 5961 | Stryker Portage, MI (ENTRY LEVEL)Design Engineer, Electrical Bachelor's degree in EE or related discipline Exp: 0+ years |
Work cooperatively with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success and contribute to the project as a team member Learn procedures, policies, processes, systems, and technology required\ Work on problems in limited scope; purposefully learn while gaining experience Demonstrate ownership and integrity of work Build stable relationships | 10/4/2022 |
| 5962 | Acrotech Biotech East Windsor, NJ LABORATORY TECHNICIAN Bachelor Degree in related scientific field Exp: 1-3 years |
Microbiologist will perform a variety of Microbiology testing to assess the strength, identity and purity of test samples and/or materials. The Microbiologist will work as a member of team to effectively plan and Microbiology testing using established (official in USP and/or in-house) test procedures. The Microbiology may execute 90% - 100% of their work at the bench level. | 10/4/2022 |
| 5963 | Acrotech Biotech East Windsor, NJ MICROBIOLOGIST I Bachelor Degree in related scientific field Exp: 1-3 years |
Microbiologist will perform a variety of Microbiology testing to assess the strength, identity and purity of test samples and/or materials. The Microbiologist will work as a member of team to effectively plan and Microbiology testing using established (official in USP and/or in-house) test procedures. The Microbiology may execute 90% - 100% of their work at the bench level. | 10/4/2022 |
| 5964 | Acrotech Biotech East Windsor, NJ ASSOCIATE CHEMIST II BS with Chemistry Exp: 1-3 years |
Chemist will perform a variety of QC testing to assess the strength, identity and purity of test samples and/or materials. The Chemist will work as a member of team to effectively plan and QC analytical testing using established (official and/or in-house) test procedures. The Chemist may execute 90% - 100% of their work at the bench level. | 10/4/2022 |
| 5965 | Acrotech Biotech Dayton, NJ ASSOCIATE CHEMIST II (TEMP) BS with Chemistry Exp: 1-3 years |
Chemist will perform a variety of QC testing to assess the strength, identity and purity of test samples and/or materials. The Chemist will work as a member of team to effectively plan and QC analytical testing using established (official and/or in-house) test procedures. The Chemist may execute 90% - 100% of their work at the bench level. | 10/4/2022 |
| 5966 | Cell Signaling Technology Danvers, MA Research Associate (Monoclonal Development) Bachelors degree in cell biology or immunology preferred Exp: 1+ years |
The Research Associate is a member of the Monoclonal Development team which is a core function for antibody development at CST. This individual will be responsible for screening XMT and mouse fusions to provide monoclonal antibody clones with the best utilities possible to be developed into final products. This position will focus on an early step in our product development process and will enable broad exposure to the full monoclonal antibody development process. | 10/5/2022 |
| 5967 | Civetta Therapeutics Cambridge, MA Cell Biology Research Associate BS in Biology, Molecular Biology, Biochemistry, or related Life Science discipline Exp: 1-3 years |
We are seeking a highly-motivated Research Scientist to help support our chemical biology efforts at Civetta. This candidate will help us discover small molecule modulators of beta-propeller proteins, support validation of new targets, and help propel our ongoing drug discovery programs. This is an excellent opportunity for individuals looking to work in a fast-paced, dynamic biotech environment. | 10/5/2022 |
| 5968 | Repligen Hopkinton, MA Process Engineer Engineering degree or equivalent required Exp: 0-3 years |
We are seeking motivated and experienced process engineer who will focus on multiproduct manufacturing support, project execution, validation, and tech transfer. The position is based in Massachusetts and will be focused on Process support & development for multiple product lines within the field of bioprocessing. This individual will work closely with Manufacturing and R&D to improve current and new products. The successful candidate will play a key role in ensuring that the department's production and quality goals are met. The applicant will be the key interface between manufacturing, quality and R&D. Hands-on mechanical aptitude and an exceptional problem-solving ability are important. | 10/5/2022 |
| 5969 | Rho Durham, NC Research Associate, Federal Research Bachelor’s degree in a scientific field or a related area of study with research emphasis Exp: entry-level |
The Research Associate will assist project managers in day-to-day operations of either federally-funded or commercial studies. This is an entry-level position. This is not a laboratory research position. | 10/5/2022 |
| 5970 | WuXi Apptec San Diego, CA Research Associate II Bachelors in Life Sciences or related field. Exp: 1 to 2 years |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its IO in vitro Division. We are seeking a highly skilled and motivated Research Associates to help advance HD Biosciences’ immuno-oncology team to complete client-based projects and experiments. | 10/5/2022 |
| 5971 | WuXi Apptec Cranbury, NJ Associate Scientist I Bachelor's degree in chemistry or closely related physical science Exp: 0 - 3 years |
The Associate Scientist I is responsible to conduct and/or provide support for various types of in vitro ADME assays in support of discovery and development programs in the DMPK department. | 10/5/2022 |
| 5972 | WuXi Apptec Cranbury, NJ Associate Scientist II Master’s degree in animal science, biology, or a related scientific discipline. Exp: 0 -1 years |
Plans and carries out in vivo experiments and associated research assignments in rodents. Maintains the vivarium, labs, and program to AAALAC and other standards. Operates lab equipment including oxidizers, centrifuges, LS counters, cage/tunnel washers, infusion pumps, etc. | 10/5/2022 |
| 5973 | WuXi Apptec San Diego, CA Research Associate I Bachelors preferred Exp: 0-1 years’ |
We are growing and seeking a motivated Research Associate I to support our in vivo pharmacology team for various projects. | 10/5/2022 |
| 5974 | WuXi Apptec San Diego, CA Research Associate I - In Vivo Pharmacology Master degree in Molecular and Cell Biology or Bachelor degree Exp: 1 -2 year |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly skilled and motivated Research Associate I to support our in vivo pharmacology team for various projects. | 10/5/2022 |
| 5975 | WuXi Apptec San Diego, CA Research Associate II - In Vivo Pharmacology Master degree in Molecular and Cell Biology or Bachelor degree Exp: 1 -2 year |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly skilled and motivated Research Associate II to support our in vivo pharmacology team for various projects. | 10/5/2022 |
| 5976 | Catamaran Bio Boston, MA Research Associate / Senior Research Associate, Cell Culture BS or certificate in biology, biotechnology, or equivalent/related disciplines. Exp: 1-5 years |
Catamaran is seeking an experienced, hands-on Research Associate / Senior Research Associate to support Catamaran’s development of an allogeneic NK cell drug product. The successful candidate will be responsible for generating and maintaining stocks of cell lines used for in vitro and in vivo assays, including feeder cells, tumor cell lines, NK cells and genetically modified cells. This work involves cell isolation, expansion, engineering, harvest and cryopreservation. This role will require collaborating extensively with Research and CMC teams. The ideal candidate has relevant experience in cell culture of primary human cells and cell lines, and is excited to join a small, fast-paced team with a “can-do” attitude to drive forward our new cell therapy platform. | 10/5/2022 |
| 5977 | Catamaran Bio Boston, MA Research Associate/Senior Research Associate, Cell Process Bachelors or master’s degree in chemical engineering, immunology, biology, synthetic biology, chemical biology, biochemistry, pharmaceutical sciences, Exp: 0-2 years’ |
The Cell Process Team is seeking a talented, diligent, and collaborative research associate to execute and design cell expansion process activities for the advancement of our best-in-class CAR-NK Cell Therapies for Oncology and other diseases. Cell Process works to ingeniously solve the challenges associated with the allogeneic manufacture of CAR-NK cell therapies including cell isolation/enrichment; cell engineering and gene editing; and cell expansion. They will be responsible for the operation of a clinical-scale bioreactor process design for the expansion of clinical CAR-NK candidates, execution of cell-based assays for in-process characterization, and technical process transfer to internal and external manufacturing sites in support of Phase 1 clinical activities. The ideal candidate is a self-motivated and technically competent process development scientist or engineer with an interest in bioreactor design and control, who is excited to join a small, fast-paced team with a “can-do” attitude to drive forward our new cell therapy platform. This is a unique opportunity to realize the promise of allogeneic cell therapy manufacturing paradigms and bring the TAILWIND platform to life at a clinical scale. | 10/5/2022 |
| 5978 | Cel-Sci Baltimore & Elkridge, MD Validation Engineer B.S. in a related discipline Exp: 1 to 5+ year |
The Validation Engineer is responsible for the regulation and support of equipment and systems. Assists in equipment selection, specification, and negotiating fees. Maintains all records related to qualification and validation. Works on projects where data analysis requires evaluation of defined factors to broad concepts. Utilizes independent judgment within broad parameters to determine an appropriate solution. Prepares validation reports, suggests and assists in determining specifications, and makes recommendations for modifications as necessary. The Validation Engineer reports to the Validation Supervisor. | 10/6/2022 |
| 5979 | Circle Pharma South San Francisco, CA Research Associate/Sr. Research Associate, Analytical Chemistry M.S. degree in Chemistry, Biology or a related scientific discipline Exp: 0+ years |
We are looking to add a Research Associate or Senior Research Associate to our growing Chemistry team. Reporting to our Director of Analytical Chemistry, this RA will be responsible for the purification and analysis of target molecules, as well as routine instrument maintenance. Our ideal candidate will have experience in small molecule/peptide purification and analysis. Our ideal candidate will also have a proven track-record of productivity and project ownership, coupled with a solid understanding of small molecule/peptide purification and analysis techniques. | 10/6/2022 |
| 5980 | Concuir Consulting Los Angeles (Hybrid), CA ASSOCIATE CONSULTANT – ENGINEER I/II Bachelors or higher in Engineering or Science Exp: 0-2+ years’ |
As a full-time employee of Concuir, Inc, you will provide consulting services to pharmaceutical, biotech and/or medical device clients. In this role, you will quickly learn client typical practices and be in a position to recommend and implement improvements to reach project goals. This is based on your experience as well as from Concuir’s portfolio of project management and cGxP best practices. Typical projects range from design through qualification of production equipment and/or utilities to modification or implementation of new facilities and process scale ups. | 10/6/2022 |
| 5981 | CorneaGen Seattle , WA Laboratory Assistant/Transporter (On-Site) B.S. degree in a life science field education is a bonus. Exp: Entry-Level |
The Laboratory Assistant/Transporter plays a vital role by ensuring packages are delivered and received on time. As a Laboratory Assistant/Transporter, you will be responsible for delivering corneal tissue to local destinations via company vehicle and retrieving packages from the airport and local hospitals. Additionally, this role supports the laboratory in our Seattle office by ordering and stocking supplies, ensuring the lab is clean, and assist with packing tissue in accordance with department protocols. On a daily basis, this position helps ensure that our customers - surgeons all across the world - are able to get what they need when they need it so that they can successfully complete their corneal transplant surgeries for their patients and help them regain their eyesight. If you're the type of individual who enjoys driving and prides yourself on driving safely, this is an opportunity to apply your skills and experience and truly make a difference in people's lives! | 10/6/2022 |
| 5982 | Cytokinetics South San Francisco, CA Research Associate, Medicinal Chemistry BS/MS in Chemistry Exp: 0-3 years |
We are currently seeking a Research Associate for our Medicinal Chemistry department. As a Research Associate, you will thrive as a highly motivated and creative scientist! This is an exciting opportunity to be part of a growing, dynamic, and highly collaborative R&D team involving novel target approaches to find medicine for unmet medical needs! Our Research Associates collaborate with scientific mentors in a one-on-one reporting structure to design and efficiently synthesize target molecules for evaluation as potential drug candidates. You will collaborate with a broad group of highly experienced scientists and focus on advancing drug discovery research programs to the stage of clinical development. | 10/6/2022 |
| 5983 | CytomX Therapeutics South San Francisco, CA TEMP Research Associate, Protein Purification, Protein Sciences MS in Biochemistry Exp: 1 year |
We seek a highly motivated individual to support the protein production, purification and analytical method development needs for all the discovery programs at CytomX. The successful candidate will work as a TEMP Research Associate in the Protein Sciences Department up to 12 months and contribute to the lead selection process for all discovery pipeline programs including Probodies, Bispecifics and cytokines. | 10/6/2022 |
| 5984 | Debut Biotechnology San Diego, CA Research Associate: Protein Expression and Purification Master’s degree in Biology, Chemistry, Biochemistry, or other related disciplines Exp: 1+ years |
Debut Biotechnology is hiring a full-time research associate in protein expression and purification focused on cell-free biotherapeutic production. The successful candidate will work in a fast-paced team to create and test new enzymes for biotherapeutic creation and modification. Candidates must demonstrate a sense of urgency, contagious optimism, and a can-do attitude. They must lead by example and hold themselves and others accountable while maintaining productive and professional relationships within the team. We are looking for candidates with a sense of urgency, contagious optimism, and a can-do attitude. They must lead by example and hold themselves and others accountable while maintaining productive and professional relationships within the team. | 10/6/2022 |
| 5985 | Decipher Biosciences San Diego, CA Clinical Lab Technician Bachelor’s degree required Exp: 1 years’ |
The Clinical Lab Technician’s primary responsibility is to provide front-line support in the procurement of record of loan (ROL) material and manage chain-of-custody of samples received. This individual must support the Decipher internal and external customers in the routine functions to ensure client satisfaction and appropriate records and materials management are consistently maintained. This individual must work with staff to employ a team approach. Manages patient orders with or without samples and oversees special projects assigned by their supervisor. | 10/6/2022 |
| 5986 | Decipher Biosciences San Diego, CA Research Associate I, Assay Development B.Sci. in biological sciences (or related field) Exp: 1-2 years |
The Research Associate I will support the Assay Development team at Decipher Biosciences; assisting in research, development, and optimization of genomic assays, and supporting general laboratory maintenance and document control. Other responsibilities might be applied as needed. | 10/6/2022 |
| 5987 | Deepcell Menlo Park, CA Research Associate/Senior Research Associate, System Integration Bachelor’s or Master’s degree in Bioengineering, Biomedical Engineering, or similar subject is required Exp: one year |
Come join Deepcell and make a difference! We're a small team of passionate innovators in biomedical engineering, artificial intelligence, molecular biology, and genomics. Our technology has won multiple prestigious awards and is backed by top-tier venture capitalists in Silicon Valley. | 10/6/2022 |
| 5988 | DiabetOmics Hillsboro, OR Research Assistant/Associate in Product Development (2 positions available immediately) BA/BS in a relevant biological science Exp: 1-2 years |
Diabetomics, Inc., is a leading medical diagnostics company serving the needs of personalized health and diabetes risk assessment and management. Diabetomics R&D group is currently seeking a Research Assistant/Associate to join our established team. Essential Functions: Supports the Diagnostic Product Development team. This is a hands-on, bench-level laboratory position. Tasks will include, but are not limited to: assay feasibility, assay development, optimization, reagent formulation, verification and validation studies. | 10/7/2022 |
| 5989 | DxTerity Rancho Dominguez, CA Laboratory Technician/Scientist Molecular Biology, Lab Operations S. or M.S. in chemical, biological or clinical laboratory science, or medical technology from an accredited institution. Exp: 1-3 years |
Testing biological specimens in molecular biology laboratory environment, including high throughput workflows, analyzing the results, and preparing them for reporting. | 10/7/2022 |
| 5990 | Eclipse Bioinnovations San Diego, CA Bioinformatics Associate B.S. or M.S. in Bioinformatics, Computational Biology, Computer Science, Biology, or related discipline Exp: entry level |
This is an entry level position with opportunity for growth for candidates who are looking to work in the RNA field and develop their bioinformatics skills. Candidates should be highly motivated, eager to learn, and capable of communicating effectively. The primary role of a bioinformatics associate is to assist project leads with both customer and R&D analyses. | 10/7/2022 |
| 5991 | Ensoma Boston, MA Analytical Development Associate Scientist BS or MS Degree in Biology, Cell Biology, Molecular Biology or Biochemistry. Exp: 1+ years |
We are seeking a highly motivated Analytical Development Associate Scientist to join our CMC team. In this Associate Scientist role, your main responsibilities will include supporting analytical assay development and sample evaluation to enable vector production and process development teams to make informed decisions to drive drug substance and drug product development. This position will support the CMC team by performing cell culture and wet lab experiments, analyzing data, drafting protocols, procedures, and reports. A successful candidate will be responsible for planning experiments, executing protocols and will be able to summarize results independently. Should the need arise, troubleshooting experimental protocols and in collaboration with his/her supervisor and effectively implementing changes to the protocol. In this position, collaborations both within analytical development and in cross-functional groups are key to advancing novel gene therapies into the clinic.A successful candidate will be responsible for planning experiments, executing protocols and will be able to summarize results independently. Should the need arise, troubleshooting experimental protocols and in collaboration with his/her supervisor and effectively implementing changes to the protocol. In this position, collaborations both within analytical development and in cross-functional groups are key to advancing novel gene therapies into the clinic.We are seeking a highly motivated Analytical Development Associate Scientist to join our CMC team. In this Associate Scientist role, your main responsibilities will include supporting analytical assay development and sample evaluation to enable vector production and process development teams to make informed decisions to drive drug substance and drug product development. This position will support the CMC team by performing cell culture and wet lab experiments, analyzing data, drafting protocols, procedures, and reports. | 10/7/2022 |
| 5992 | Etubics Culver City, CA Research Associate B.S. in biochemistry or in related scientific disciplines Exp: 1-2 years |
ImmunityBio Inc. is seeking a highly motivated, full-time research associate to join the Protein Science group to support the discovery, research and development of immunotherapies across multiple therapeutic areas, including, but not limited to cancer and infectious diseases. The ideal candidate should have a bachelor’s degree with 1-2 years of wet-lab experiences, ability to manage multiple tasks in a timely manner, good written/verbal communication skills and have a willingness to work as part of the team. | 10/7/2022 |
| 5993 | Etubics Culver City, CA Research Associate II B.S. in biochemistry or in related scientific disciplines Exp: 1-3 years |
ImmunityBio Inc. is seeking a highly motivated, full-time research associate to join the Protein Science group to support the discovery, research and development of immunotherapies across multiple therapeutic areas, including, but not limited to cancer and infectious diseases. The ideal candidate should have a bachelor’s degree with 1-3 years of wet-lab experiences or a master’s degree with 1+ year of wet-lab experience, ability to manage multiple tasks in a timely manner, good written/verbal communication skills and have a willingness to work as part of the team. | 10/7/2022 |
| 5994 | Evelo Biosciences Cambridge, MA Formulation Research Associate B.S. or M.S in Pharmaceutical Sciences, or Chemical Engineering preferred Exp: 1-5 years’ |
Evelo Biosciences is seeking a Formulation Research Associate to support our dynamic and growing organization. Evelo Biosciences, Inc. (Nasdaq: EVLO) a biotechnology company developing a new modality of orally delivered, systemically acting biologics that could disrupt the industry is looking for a highly motivated individual who is energized by the prospect of working in a clinical stage company, has a strong desire to learn, and wishes to be an integral member of an interdisciplinary team. This critical role will be responsible for providing essential scientific support to the Formulation Team in a fast-paced, dynamic and intellectually challenging environment. The successful candidate should have basic knowledge of chemistry and be proficient in standard laboratory operations such as weighing, mixing, characterizing powders, conducting experiments, performing data analysis, draft reports, present results, and possess the ability to multi-task within scope in a timely manner. | 10/7/2022 |
| 5995 | Flexion Therapeutics San Diego, CA QA Associate 2 - Raw Materials BS/BA degree in scientific discipline from an accredited college or university or equivalent experience. Exp: 1-3 years |
This person is to assist and support the organization with GMP compliance; monitoring of conformance to established quality assurance processes and GMP standards in release of raw materials. | 10/7/2022 |
| 5996 | Fluxenergy Irvine , CA Research Associate - Microfluidics, Irvine Bachelor of Science degree or Master's degree in Life Science or Engineering disciplines or related fields Exp: 0-2 years |
As a Research Assistant at Fluxergy, you will be directly iinvolved in the company's Card R&D activities, as well as deeply involved with the company's long-term strategy. You will be repsonsible for helping develop the next generation of Fluxergy Test Card, a microfluidic consumable aiming at transforming point-of-care diagnostic systems. You will be expected to conduct, analyze, and report on experiments to develop new Test Card from feasibility through validation for the Fluxergy platform. You will work closely with a cross discipline team of R&D and Production Engineers and Technicians to develop new products. This position requires a highly motivated, independent worker who has a strong desire to bring products to the market. | 10/7/2022 |
| 5997 | Fluxenergy Irvine , CA Industrial Engineer, Irvine Bachelor’s degree or Masters' degree in Industrial Engineering Exp: 1-3 years |
As the Industrial Engineer at Fluxergy, you will be directly involved in the company’s Production activities, as well as deeply involved with the company’s long-term strategy. You will be responsible for process improvement, scale up and capacity planning while working with a small but passionate team. This position requires a deep, in-depth knowledge of lean manufacturing and six sigma methodologies. | 10/7/2022 |
| 5998 | Fluxenergy Irvine , CA Process Engineer, Irvine Bachelor's Degree or Master's Degree in an engineering field Exp: 0-2 Years |
As the process engineer at Fluxergy, you will be directly involved in the company’s production activities, as well as deeply involved with the company’s long-term strategy. You will be responsible for process ownership while working with a small but passionate team. This position requires a deep, in-depth knowledge of manufacturing processes, stability and process control. | 10/7/2022 |
| 5999 | Foghorn Therapeutics Cambridge, MA NEW Research Associate - Biochemistry Biophysics BA/BS or MS degree in Biochemistry or Biophysics, or life sciences or biotechnology Exp: 1-3yrs+ years |
Foghorn is seeking a highly motivated, enthusiastic, and collaborative Research Associate to join our Drug Discovery team in a lab-based role to support early discovery projects in oncology. As a member of our Drug Discovery team the candidate will have an opportunity to employ various biochemical and biophysical assay technologies in mechanism of action studies, screening, and hit validation. Training is provided. This job is onsite and located in Cambridge, MA. | 10/7/2022 |
| 6000 | Foghorn Therapeutics Cambridge, MA Senior Research Associate - Translational Biomarkers Master of Science Exp: 1 year or more |
Conduct exploratory research to help identify new tumor- and peripheral-based biomarker assays for emerging clinical programs utilizing in vitro/ex vivo/in vivo model system Work with Biology and Pharmacology groups to acquire, process, and analyze samples to generate internal datasets necessary for assay development and pre-clinical proof of concept for clinical biomarkers (e.g. qPCR, FACS, ELISAs, etc.) Test new technologies in house and develop exploratory assay systems to answer key questions relevant to Translational Biomarker Plans for Clinical Programs | 10/7/2022 |
| 6001 | Capricor Therapeutics Los Angeles, CA Manufacturing Associate I/II Bachelor’s degree in Biomedical Engineering, Biological Sciences or related field Exp: 1-3 years |
This position is immediately available to join our Manufacturing team to perform cGMP manufacturing to support Capricor’s clinical trials and exosome development. Capricor is developing its exosome technology as a next-generation therapeutic platform. The Company’s current focus is on developing exosomes capable of delivering nucleic acids, including mRNA as well as proteins, to treat or prevent a variety of diseases. We are seeking an individual with a scientific background, mammalian cell culture and cGMP experience. | 9/27/2022 |
| 6002 | Capricor Therapeutics San Diego, CA Manufacturing Associate I/II Bachelor’s degree in Biomedical Engineering, Biological Sciences or related field Exp: 1-3 years |
This position is immediately available to join our Manufacturing team to perform cGMP manufacturing to support Capricor’s clinical trials and exosome development. Capricor is developing its exosome technology as a next-generation therapeutic platform. The Company’s current focus is on developing exosomes capable of delivering nucleic acids, including mRNA as well as proteins, to treat or prevent a variety of diseases. We are seeking an individual with a scientific background, mammalian cell culture and cGMP experience. | 9/27/2022 |
| 6003 | CareDx Brisbane, CA Clinical Lab Assistant | Job # 1111 BS/BA in a biology-related science is preferred Exp: 1-3 years |
Clinical Laboratory Assistant (Tuesday-Saturday) The Clinical Laboratory Assistant (CLA) performs a variety of laboratory and administrative tasks to support the clinical laboratory staff in the CLIA-certified CareDx laboratory. A CLA performs laboratory duties under direct and constant supervision of a licensed CLS or the Clinical Laboratory Manager (CLM) and/or designee, who provides specific instruction regarding how tasks are to be completed and defines the steps to be employed | 9/27/2022 |
| 6004 | CareDx Brisbane, CA Clinical Lab Assistant | Job # 1455 BS/BA in a biology-related science is preferred Exp: 1-3 years |
Clinical Laboratory Assistant (Tuesday-Saturday, 2PM - 10:30PM) The Clinical Laboratory Assistant (CLA) performs a variety of laboratory and administrative tasks to support the clinical laboratory staff in the CLIA-certified CareDx laboratory. A CLA performs laboratory duties under direct and constant supervision of a licensed CLS or the Clinical Laboratory Manager (CLM) and/or designee, who provides specific instruction regarding how tasks are to be completed and defines the steps to be employed. | 9/27/2022 |
| 6005 | Abcam Fremont, CA Research Associate/Sr. Research Associate BS Degree in biochemistry, pathology, cell and molecular biology, immunology or other Life Sciences. Exp: 0-3 years |
Focus on the development and validation of qualified antibodies for IVD immunohistochemistry (IHC) applications under FDA and MDSAP/ISO13485 (2016) quality standards. | 9/27/2022 |
| 6006 | Abcam Eugene, OR Research Associate B.S. in Biology, or closely related discipline Exp: 1 year |
We are seeking a Research Associate to assist in the development of novel immunoassays in our Eugene, OR facility. The core responsibility will be to provide support to the SimpleStep immunoassay development team through the use of antibody-based laboratory techniques such as sandwich ELISA, Western blot, immunocytochemistry, and flow cytometry as well as the generation of biological materials for analysis. | 9/27/2022 |
| 6007 | Bachem Torrance, CA Production Chemist BS degree in Chemistry or related field Exp: 1-5 years’ |
The Chemist function is to develop the peptide manufacture process, manufacture GMP material and perform related activities at Bachem. | 9/28/2022 |
| 6008 | Bachem Vista, CA Production Chemist BS degree in Chemistry or related field Exp: 1-5 years’ |
The Chemist function is to develop the peptide manufacture process, manufacture GMP material and perform related activities at Bachem. | 9/28/2022 |
| 6009 | BioMarin Pharmaceutical Novato, CA Research Associate I Bachelor’s Degree in Chemistry, Biochemistry, Analytical Chemistry, or a related field Exp: 0 - 2+ years |
The selected candidate will work in the Analytical Sciences group to assist in the advancement of BioMarin’s therapeutics for clinical evaluation and potential commercialization. The candidate will be responsible assay development, assay qualification, and characterization testing using routine and semi-routine analytical methods under limited supervision. The selected candidate should possess excellent analytical, organizational and communication skills and be a self-starter willing to work efficiently and collaboratively in a dynamic environment. | 9/28/2022 |
| 6010 | Bristol-Myers Squibb Devens, MA QC Microbiology Associate BS/BA in biological sciences, or its equivalent in experience. Exp: 0 to 2 years |
This position is Wednesday through Saturday 1st shift position. 7am-5pm | 9/28/2022 |
| 6011 | Bristol-Myers Squibb Seattle, WA Research Associate- Cell Core B.S. in Biology, Chemical Engineering, Bioengineering or relevant scientific discipline Exp: 0-2 years |
Cell Core is responsible for supplying cellular products to support internal development organizations. This role will be responsible for fielding requests for cellular products and managing communications related to coordination and fulfillment of requests in support of Quality and Analytical Development functions. These communications will occur within and between varied company levels and internal organizations. The role will therefore require a high degree of approachability and interpersonal savvy, with a proven ability to work in cross-functional teams. Effective organizational skills will also be necessary as the candidate will be responsible for operating within the request fulfillment schedule, documenting operating activities, and organizing large quantities of data. Experience culturing mammalian cells is strongly preferred. | 9/28/2022 |
| 6012 | Bristol-Myers Squibb New Brunswick, NJ BACTERIOLOGIST Bachelors' degree with a major in biology, or an allied science and coursework in microbiology from an accredited college or university. Exp: 1 year |
Performs microbiological testing to ensure that the proper standards of quality are maintained. Performs microbiological, bacterial endotoxin, total organic carbon and conductivity analyses of water system samples. Performs environmental monitoring and water sampling in support of the routine operations and manufacturing. Demonstrates the use of aseptic technique. Analyzes, develops and recommends new methods for the improvement of various standard assays and tests. Carries out analytical tests and inspections in connection with the investigation of product and environmental monitoring excursions. Evaluates results and submits documentation for approval. Performs routine maintenance and calibration procedures on laboratory instrumentation. Troubleshoots equipment and methods for investigational purposes. Performs laboratory support activities such as stock culture maintenance and laboratory inspections, as assigned. Responsibilities include maintaining laboratory documentation, samples, and equipment under strict compliance with safety, GMP, federal, state and local regulations. Maintains laboratory notebook (paper or electronic), record/capture records raw data, calculates results and submit results to laboratory supervisor and/or computer database following Good Documentation Practices. | 9/28/2022 |
| 6013 | Bristol-Myers Squibb Phoenix, AZ Analyst I Bachelor’s Degree, particularly in Microbiology or Science related field, preferred. Exp: 1 year |
The Analyst I, QC Microbiology, is responsible for routine and non-routine microbiological testing and environmental monitoring in support of sterile product manufacturing. The Analyst I is also responsible for peer review, training, supporting document management, projects, CAPAs and investigations in accordance with the organization’s policies, procedures, and state, federal and local laws and ensure compliance with current Good Manufacturing Practices (cGMP), USP, EP, JP and other regulatory requirements at all times. | 9/29/2022 |
| 6014 | Bristol-Myers Squibb Seattle, WA Associate/Senior Associate Scientist, Analytical Operations- Cell Therapy Associate scientist requires BS in a scientific discipline; Sr Associate scientist requires MS in a scientific discipline. Exp: BS: 1+ year ; MS: 1+ years |
Cell Therapy Product and Analytical Development (P&AD) is seeking an enthusiastic, self-driven Associate/Senior Associate Scientist to join its Analytical Operation team that values data quality, high productivity and team‐work . In this individual contributor, lab-based role, the Associate/Senior Associate Scientist will work in a collaborative environment to perform various analytics testing for process development and product characterization to support BMS cell therapy programs. This position will report to the supervisor of Analytical Operation. The successful candidate must have hands on experience with various bioanalytical techniques including ELISA, qPCR, ddPCR and flow cytometry and the ability to interface with multiple groups, the ability to independently perform tasks, interpret results, and troubleshoot. | 9/29/2022 |
| 6015 | Bristol-Myers Squibb Summit, NJ Assistant / Associate / Sr. Associate Scientist, Biologics Manufacturing – Downstream Operations Biology, Biochemistry, Bioengineering, Biochemical, Chemical Engineering or related discipline. Assistant Scientist - BA/BS ; Associate Scientist – MA Exp: BA/BS: 0-2 yrs; MA/MS: 0-2 years |
We are currently looking for an Assistant Scientist, Associate Scientist OR Senior Associate Scientist to join our Biologics Manufacturing Team within the BMS’s Biologics Development & Manufacturing group in Summit, New Jersey. As a member of the Biologics Development & Manufacturing group, the Assistant / Associate / Sr. Associate Scientist will provide technical and operational expertise and oversight to early stage clinical manufacturing campaigns. The focus of this position will be on downstream operations and support of upstream operations in single-use manufacturing environment. | 9/29/2022 |
| 6016 | Covance Somerset, NJ Study Technician - Animal Operations Bachelor Degree Exp: No experience is required |
In this animal-based role, you’ll collect, document and manage data that includes animal observations, test material administration and clinical samples. This is a hands on, physically demanding role working directly with animals daily. | 9/29/2022 |
| 6017 | Covance Madison; Somerset; Greenfield, WI Study Technician- Animal Operations (3 locations) Bachelor degree in Life Sciences Exp: current student |
**Applicants for this role must be a current student with intentions to graduate between December 2022 and May 2023** In this animal-based role, you’ll collect, document and manage data that includes animal observations, test material administration and clinical samples. This is a hands on, physically demanding role working directly with animals daily. | 9/29/2022 |
| 6018 | Covance Madison; Somerset; Greenfield, WI Study Technician- Anatomical Pathology (3 locations) Bachelor’s Degree in Life Sciences, or Associate Degree in Life Sciences, Histology, Laboratory Animal Technology or Veterinary Technology; experience Exp: current student |
**Applicants for this role must be a current student with intentions to graduate between December 2022 and May 2023** In this animal-based role, you’ll collect, document and manage data that includes animal observations, test material administration and clinical samples. This is a hands on, physically demanding role working directly with animals daily. | 9/29/2022 |
| 6019 | Covance Raritan, NJ Medical Technologist/Clinical Laboratory Scientist - Molecular Associate’s or Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requir Exp: 1 year |
Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. The work schedule for this position will be Tuesday - Saturday (3:00pm – 11:30pm) | 9/29/2022 |
| 6020 | Covance Raritan, NJ Medical Technologist/Clinical Laboratory Technician – Immunology Associate’s or Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requir Exp: 1 year |
New Grads Welcome – Full Training Provided Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. The work schedule for this position will be: Tuesday - Saturday 2.00 pm to 10.30 pm – Rotating Sundays | 9/29/2022 |
| 6021 | Covance Raritan, NJ Medical Technologist/Clinical Laboratory Technician – Hematology Associate’s or Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requir Exp: 1 year |
Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. The work schedule for this position will be Monday-Friday 11:00 PM- 7:30 AM & alternating SaturdayAre you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. The work schedule for this position will be Monday-Friday 11:00 PM- 7:30 AM & alternating Saturday | 9/29/2022 |
| 6022 | Exact Sciences Phoenix, AZ Molecular Technologist I Molecular Technologist I Bachelor's Degree in Biology, Chemistry, Biochemistry, Life Sciences, or field as outlined in the essential duties. Exp: 1+ years |
The Molecular Technologist I will isolate and quantify nucleic acids, perform polymerase chain reaction (PCR) tests and next generation sequencing (NGS), library construction, and other NGS-associated procedures. | 9/29/2022 |
| 6023 | Exact Sciences Madison, WI Laboratory Service Engineer I - Tuesday-Friday, 2:00pm-1:00am Bachelor’s degree in Engineering, Technology, Molecular Biology, Electronics, or related field Exp: 1+ years |
The Laboratory Service Engineer I (LSE I) is responsible for the Instrument and Automation Services of laboratory equipment and instrumentation, including installation, calibration, maintenance, and repair. This includes both simple (e.g., orbital shakers) and complex (e.g., liquid handling robotics.) instrumentation in the various laboratory environments. These environments may include clinical laboratories, R&D laboratories, and manufacturing and quality control laboratories. The individual in this role will continuously work with other Lab Service Engineers (LSE) and the laboratory teams to ensure proper instrument function and to troubleshoot any system concerns. The LSE I may work continuously with other LSEs and the laboratory teams to ensure proper instrument function and to troubleshoot any system concerns. | 9/29/2022 |
| 6024 | Exact Sciences Cambridge, MA Laboratory Service Engineer I - $10,000 Sign-on Bonus! Bachelor’s degree in Engineering, Technology, Molecular Biology, Electronics, or related field Exp: 1+ years |
The Laboratory Service Engineer I (LSE I) is responsible for the Instrument and Automation Services of laboratory equipment and instrumentation, including installation, calibration, maintenance, and repair. This includes both simple (e.g., orbital shakers) and complex (e.g., liquid handling robotics.) instrumentation in the various laboratory environments. These environments may include clinical laboratories, R&D laboratories, and manufacturing and quality control laboratories. The individual in this role will continuously work with other Lab Service Engineers (LSE) and the laboratory teams to ensure proper instrument function and to troubleshoot any system concerns. The LSE I may work continuously with other LSEs and the laboratory teams to ensure proper instrument function and to troubleshoot any system concerns. We are offering a $10,000 sign-on bonus to external candidates. | 9/29/2022 |
| 6025 | Exact Sciences Redwood City, CA Laboratory Service Engineer I Laboratory Service Engineer I Bachelor’s degree in Engineering, Technology, Molecular Biology, Electronics, or related field Exp: 1+ years |
The Laboratory Service Engineer I (LSE I) is responsible for the service and support of laboratory equipment and instrumentation, including installation, calibration, maintenance, and repair. This includes both simple (e.g., orbital shakers) and complex (e.g., liquid handling robotics.) instrumentation in the various laboratory environments. These environments may include clinical laboratories, R&D laboratories, and manufacturing and quality control laboratories. The individual in this role will continuously work with other Lab Service Engineers (LSE) and the laboratory teams to ensure proper instrument function and to troubleshoot any system concerns. The LSE I may work continuously with other LSEs and the laboratory teams to ensure proper instrument function and to troubleshoot any system concerns. | 9/30/2022 |
| 6026 | Eli Lily Cambridge, MA Biologist-Obesity Research Master’s degree in biology or a closely related field Exp: research experience |
The Diabetes, Obesity and Complications Therapeutic Area (DOCTA) of Eli Lilly and Company, is focused on the discovery of biologic, small molecule and genetic therapeutics for the treatment of diabetes, obesity and associated complications. We are seeking an individual with training in molecular biology, cell culture and biochemistry, as well as broad experience in metabolic disease programs, who can succeed in a highly collaborative team environment. The successful candidate will play a meaningful role in supporting discovery efforts and established pipeline projects with an emphasis on anti-obesity therapeutics. You will be responsible for setting up critical capabilities in the laboratory setting and working with other scientists within and across departments to achieve project goals. We are a growing group passionate about our research and how it impacts Lilly's mission of improving lives. | 9/30/2022 |
| 6027 | Eli Lily Indianapolis, IN Chemist - SMDD MS degree in synthetic organic chemistry or related field Exp: |
Lilly’s Synthetic Molecule Design and Development (SMDD) organization engages in design and development activities for small molecules, peptides and oligonucleotides from pre-clinical phases through commercialization for drug substances and drug products. Our scientists develop solutions using their deep technical expertise to enable testing of clinical hypotheses and accelerate drug development. SMDD excels in these areas by placing innovation at the heart of what we do. Our innovation engine is driven by an array of diverse talents and cultures brought together in state of the art laboratory and open concept facilities which foster collaboration and teamwork. Our team is looking for creative candidates to contribute to our synthetic molecule route design and development portfolio | 9/30/2022 |
| 6028 | AI Therapeutics Madison, WI Associate Analytical Chemist 1st Shift - $3,000 Sign On Bonus Bachelor’s Degree in relevant field (laboratory experience may be substituted for a degree) Exp: Entry-Level |
We test of a variety of instrumentation including UPLC, HPLC, GC, and LCMS technologies. We offer an innovative and collaborative team environment, and the opportunity to develop expertise on a wide variety of analytical instruments! If you are looking for an opportunity to work for an exciting growth oriented company, we look forward to talking with you! | 9/30/2022 |
| 6029 | AI Therapeutics Cambridge, MA Research Associate (Separations + Biophysical) Bachelor’s Degree/ Master's Degree in related science Exp: BS: 0-2+ years; 0+ years |
Provide timely internal non-GMP testing support for various teams Support automation of analytical workflows and qualification of automated assays Document lab work and results in ELN and/or LIMS Coordinate, store, and properly handle samples and retains Manage and track supply of controls, reference standards, and critical reagents Train other analysts as necessary Ensure Instruments and lab are properly maintained Work with many other groups to support client's mission | 9/30/2022 |
| 6030 | AI Therapeutics Cambridge, MA Research Associate Degree in Cell and Molecular Biology, Biochemistry, Pharmaceutical, or other biological/analytical discipline Exp: BS: 0-2+ years; 0+ years |
Supports viral vector process development by providing analytical testing on DNA, ELISA, cell based platform within agreed upon turn-around Demonstrate good understanding of ongoing programs and data generated in relation to the program Troubleshoots issues as needed with supervision Monitors assay performance to ensure GLP compliance Maintains equipment and critical reagent inventory Provides testing support to aid viral vector development to support cell therapies in a fast paced and dynamic team environment. | 9/30/2022 |
| 6031 | AI Therapeutics Foster City, CA HPLC Research Associate Bachelor's/Master's Degree Exp: BS: 0 - 3 years; MS: 1+ year |
Plans and executes assigned experiments that support non-routine development activities and project goals Conduct analytical methods including UPLC/HPLC, Dissolution, GC, Thermogravimetric DSC/TGA, and KF titration Perform data analysis and troubleshoot methods and instrumentation Recommends alternatives, researches new methods and techniques and may proactively seek out senior personnel to discuss potential solutions to problems. Prepare data for presentation and assist in generating technical reports, and interact with other groups within the department Perform review and peer review of analytical data Initiate and perform investigations and development, as needed Ensure project deliverables are scientifically accurate and meet timeline expectations | 9/30/2022 |
| 6032 | AI Therapeutics Cambridge, MA Research Chemist (HPLC and CE) Bachelor’s Degree in related science; Master’s Degree in related science Exp: BS: 1-2+ years; MS: 0+ years |
Provide timely internal non-GMP testing support for various teams Support automation of analytical workflows and qualification of automated assays Document lab work and results in ELN and/or LIMS Coordinate, store, and properly handle samples and retains Manage and track supply of controls, reference standards, and critical reagents Train other analysts as necessary Ensure Instruments and lab are properly maintained Work with many other groups to support client's mission | 9/30/2022 |
| 6033 | AI Therapeutics San Diego, CA Research Associate I in vivo Bachelor’s degree in life sciences or related discipline required. Exp: 0-2 years |
The successful candidate for the Research Associate I position will join the Beacon Discovery team with a multifaceted approach for providing high value services based on the Beacon Discovery platform and other proprietary technologies. The position provides an outstanding opportunity to learn new techniques and develop skills within a dynamic in vivo pharmacology research team. We work with multiple animal models, from anxiety to metabolism and beyond. If you are interested in working in a fast paced, challenging environment where you will have an opportunity to learn and succeed this may be the place for you. Laboratory experience with animal handling and pharmacology studies would be advantageous but is not necessary. Extensive training will be provided. | 9/30/2022 |
| 6034 | Cellular Dynamics Madison, WI Facility Management Specialist/Facilities Engineer - (#398) Bachelor’s degree in engineering or construction related field, or equivalent experience Exp: One year |
We are recruiting for a Facility Management Specialist (AKA Facilities Engineer) to support our investment in and on-going operation of our cGMP, research and development, and production facilities in Madison, WI. You'll be part of the technical operations group along with other highly talented professionals at FUJIFILM Cellular Dynamics, Inc., the leader in induced Pluripotent Stem Cells (iPSC’s) technology. In this role you'll oversee all aspects of facility operation and maintenance including commissioning, qualification, maintenance, and calibration of facility, equipment, systems and utilities for all FCDI facilities. This is an excellent opportunity for qualified individuals looking to apply their technical skills and to expand their professional horizons. | 9/30/2022 |
| 6035 | Cellular Dynamics Madison, WI cGMP Biomanufacturing Specialist - (#341) Bachelor’s degree in cell biology, molecular biology, biochemistry or related technical field Exp: BS Degree |
FUJIFILM Cellular Dynamics, Inc in Madison, WI is recruiting for a cGMP bio-manufacturing specialist This role provide outstanding opportunities for talented self-motivated individuals, ideally with experience in (stem) cell biology, immunology, and/or molecular biology, who can contribute to our ongoing efforts to generate differentiated cell types from human induced pluripotent stem cells. We are most interested in connecting with qualified individuals who aspire to support the development of therapeutics and/or life science products and tools to support research endeavors. In return we provide development and support to enhance your career using cutting edge iPSC technology. | 9/30/2022 |
| 6036 | Cellular Dynamics Madison, WI Undergraduate Research Assistant - (#376) High school diploma, with relevant coursework progressing to a bachelor’s degree in biologic sciences, or related field Exp: Undergraduate |
FUJIFILM Cellular Dynamics, Inc is recruiting for undergraduate research assistants to work in our research and development, and bioinformatics facility in Madison, WI. This role provides an outstanding opportunity for a dedicated and responsible individual to learn, develop, and contribute to maintaining and improving lab operations, along with supporting research and development projects. And, as required, participate in cellular and molecular projects. Ideal candidates will demonstrate a track record of self-motivation, strong organizational skills, and dedication to their work. The role requires at least 10 hours per week of commitment with flexible scheduling, and with the ability to also work on weekends as required. | 9/30/2022 |
| 6037 | Steris Plymouth, MN Software Engineer Bachelor's Degree. Exp: 0-3 years |
The Software Engineer is responsible for the design, development and deployment of complex SQL database software intended for use as standalone databases or for use in MEDIVATORS, Cantel Medical, and STERIS medical devices. | 9/30/2022 |
| 6038 | Steris Sharon, PA Quality Engineer Bachelor's Degree in Engineering General Exp: 1-5 years |
The Quality Engineer is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. This role supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 9/30/2022 |
| 6039 | Steris Rush, NY Quality Engineer Bachelor's Degree Exp: 1-5 years |
The Quality Engineer is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. This role supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 9/30/2022 |
| 6040 | Steris Mentor, OH Cybersecurity Software Development Engineer Bachelor in Computer Engineering, Computer Science, Software Engineering, Electrical Engineering, or Cybersecurity required. (A degree in another En Exp: 1+ years |
Join an organization and a team where you can have an impact on creating a healthier and safer world. As a Software Engineer within the Infection Prevention Technology (IPT) Team you will work within a software development team to achieve and maintain the security of medical equipment connected to local hospital networks and remote applications in the cloud. You will be an active participant in the corporate cybersecurity working group to share best practices, software tools, vendor selection, and other cybersecurity related activities. The Software Engineer will also support multiple product development and product sustaining teams in security related product requirements, design specifications, risk analysis, and verification, as well as develop work instructions for the maintenance and verification of security for product software. *This role allows for hybrid work options | 9/30/2022 |
| 6041 | Ascendis Pharma Redwood City, CA Research Associate, Development Chemistry Masters Degree in organic, polymer or bio-chemistry or related field. Exp: 0-3 yrs |
The successful candidate will be responsible for conducting laboratory-based process chemistry activities to support Ascendis Pharma’s growing pipeline of pre-clinical and clinical programs. Working closely with a team of scientists and engineers in Ascendis Pharma’s Redwood City laboratory, the successful candidate will be responsible for process chemistry research and development such as process optimization and scale-up. This position offers great potential for scientific growth and gain of CMC knowledge while working on developing exciting, complex, and impactful drugs for patients. | 9/18/2022 |
| 6042 | Ascendis Pharma Redwood City, CA Research Associate, Process Development Bachelor’s degree in chemistry, biochemistry, biotechnology, or a related field or MS graduate - new grads are welcome to apply! Exp: New Grads |
In this position you will be responsible for conducting laboratory experiments related to the development, characterization, scale up of a manufacturing process for our localized delivery technology platform. Working closely with a team of scientists/engineers in our new Redwood Shores facility, the Associate Scientist will characterize and investigate novel and existing processing steps used to manufacture products in our growing portfolio. This position offers great potential for growth of scientific and drug development experience while working on exciting, complex, and impactful products | 9/18/2022 |
| 6043 | Ascendis Pharma Redwood City, CA Research Associate Bachelor’s degree in chemistry, biochemistry, biotechnology, or a related field or MS graduate - new grads are welcome to apply! Exp: New Grads |
In this position you will be responsible for conducting laboratory experiments related to the development, characterization, scale up of a manufacturing process for our localized delivery technology platform. Working closely with a team of scientists/engineers in our new Redwood Shores facility, the Associate Scientist will characterize and investigate novel and existing processing steps used to manufacture products in our growing portfolio. This position offers great potential for growth of scientific and drug development experience while working on exciting, complex, and impactful products | 9/18/2022 |
| 6044 | Astellas South San Francisco, CA Research Associate II, Cell Biology in South San Francisco, California MS Degree Exp: 0-2 years |
The primary purpose of the Research Associate II is to support all lentiviral production and immune cell manufacturing needs as well as cell biology and assay development in support of research activities. This position will work primarily in a laboratory setting with Scientist and research and discovery teams. | 9/18/2022 |
| 6045 | Astellas Westborough, MA Research Associate II, Stem Cell Research in Westborough, Massachusetts MS Degree Exp: 0-2 years' |
Performs experiments and progress research and/or development in collaboration with others. Makes detailed observations, analyzes data and interprets results. Investigates, creates and develops new methods and technologies for project advancement. | 9/18/2022 |
| 6046 | Astellas Westborough, MA Research Associate II, Cell Based Therapies in Westborough, Massachusetts MS Degree Exp: 0-2 years |
We are seeking a highly motivated and energetic Research Associate to join the Research and Development team. This candidate will assist and troubleshoot exploratory research projects by performing mammalian cell culture, cell, and molecular biology, and maintain accurate records for potential clinical applications. This position is highly collaborative, with on-the-job training to support the driven candidate's development and success. | 9/18/2022 |
| 6047 | Astellas Seattle, WA Research Associate II, Clinical Gene Editing in Seattle, Washington MS Degree Exp: 0-2 years |
The primary purpose of the Research Associate II for Clinical Gene Editing is to support the generation of clinical-grade, gene-edited Universal Donor Cells in a controlled manufacturing environment. This Research Associate II role will work as part of a team planning and executing all aspects of gene-editing and engineering of pluripotent stem cells. Will assist with complex laboratory operations, keep appropriate documentation including lab notebooks, batch documentation and experimental summaries. Will be able to execute protocols with minimal guidance and will have the ability to summarize results independently. May assist in generating content and preparing controlled documents and data summaries. This position will acquire further versatility in routine procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. | 9/19/2022 |
| 6048 | Astellas Seattle, WA Research Associate II, Process Development in Seattle, Washington MS Degree Exp: 0-2 years |
The primary purpose of the Research Associate II for Process Development is to execute experiments to improve clinical-grade, gene-editing processes of Universal Donor Cells and to provide data for CMC documents. This Research Associate II role will work as part of a team evaluating processes, and planning/executing experiments to evaluate all aspects of culturing, gene-editing, and processing of pluripotent stem cells. This position will be provided training to perform all required fundamental skills. Will assist with complex laboratory operations, keep appropriate documentation including lab notebooks, batch documentation and experimental summaries. Will be able to execute protocols with minimal guidance and will have the ability to summarize results independently. May assist in generating content and preparing controlled documents and data summaries. This position will acquire further versatility in routine procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. | 9/19/2022 |
| 6049 | Astellas Seattle, WA Research Associate II, Cell Analytics in Seattle, Washington MS Degree Exp: 0-2 years |
We are seeking a highly capable, self-motivated Research Associate II for our Core Technologies Department. This individual will contribute to the molecular engineering and characterization for our gene edited Universal Donor Cells, by utilizing various cell culture techniques. They will work as a key member on a fast paced team to culture pluripotent stem cells as well as run cellular assays to characterize our proprietary Universal Donor Cells. | 9/19/2022 |
| 6050 | Aurora Biolabs San Diego, CA Research Associate I Bachelors or Masters Exp: 0-1 years |
Aurora Biolabs, LLC is seeking a motivated research associate I in cell and molecular biology, biochemistry or related field in San Diego, CA. The individual will be a critical part of our products development team, development a new line of recombinant protein products for drug discovery and commercial use. This position requires extensive hands-on experience with a broad range of techniques including protein expression and purification, molecular cloning, PCR, mammalian cell, insect cells and bacterial culture, ELISA, as well as in vitro cell-based/immuno-based assays. You will work in an atmosphere that is stimulating, innovative, and customer focused. | 9/19/2022 |
| 6051 | Avedro San Clemente, CA MANUFACTURING TECHNICIAN III, PHARMACEUTICAL bachelor’s degree in science or engineering. Exp: 0+ years’ |
Follow, execute, and adhere to documentation in accordance with cGMP, QSR, and GDP requirements: protocols, specifications, work instructions (WIs), standard operating procedures (SOPs), BRs, and DHRs. | 9/19/2022 |
| 6052 | Avitide Lebanon, NH Manufacturing Technician Bachelor degree in Biotechnology or Biology (or related field) Exp: 1-2 years’ |
This qualified candidate will join the growing manufacturing team responsible to produce Avitide AVIPure® biopharmaceutical affinity chromatography products. The individual will be involved in all aspects of product manufacturing including buffer preparation, reactor set-up, production, product packaging and cleaning. Work will be performed in accordance with established manufacturing practices and procedures in compliance with our ISO 9001 quality regulations and guidelines. Avitide seeks candidates who are highly self-motivated and can work in a collaborative fashion with other interdisciplinary team members in a fast-paced and exciting work environment. | 9/20/2022 |
| 6053 | Axial Therapeutics Woburn, MA Research Associate/Senior Research Associate - Biosciences Bachelor’s degree in biology, biochemistry, or a related field preferred. Exp: 1-3 years |
In this role the Research Associate will support biology as a member of a highly matrixed drug discovery team and will be responsible for the execution and troubleshooting of various cell-based and biochemical assays and experiments. The Research Associate will contribute to drug screening and mechanism-of-action studies for projects in immuno-oncology and neurological diseases and disorders and have opportunities to contribute to new target discovery and validation. This proactive researcher will collaborate with team members, identify opportunities to improve efficiency, share ideas and expertise and contribute to Axial’s creative, dynamic, and collaborative culture. | 9/20/2022 |
| 6054 | Azzur Totowa, NJ Chemist of Research and Development (1-3 years experience) M.Sc. or BS in Chemistry or Chemical Engineering is required. Exp: 1-2 + years |
• Develop new chemical methods for analysis and equipment for implementation purposes. • Develop analytical methods for process solutions used in metal deposition and other areas of semiconductor manufacturing. • Interface with engineering group to design commercial analyzers. • Plan and conduct experiments then write technical report findings. • Participate in documenting, testing and supporting equipment. • Validate analytical methods developed in R&D department, update documentation and prepare reports. • Prepare scientific publications and present work at conferences. | 9/20/2022 |
| 6055 | Berkshire Sterile Manufacturing Lee, MA Process Engineering Associate Process Engineer: Bachelor’s degree in Chemical Engineering, Chemistry, Biology, or Pharmaceutical Science Exp: (1) year |
The Process Engineer will lead tech transfer projects from client or small scale to manufacturing/large scale in a manner that meets safety, quality, and operational performance expectations. The key function of this role will be to deliver effective, safe and efficient manufacturing processes for parenteral drug products. | 9/20/2022 |
| 6056 | Biocare Medical Pacheco, CA Associate I, Protein Chemistry Bachelor’s degree in a scientific field Exp: one plus (1+) years’ |
The Protein Chemistry Associate I will take an active role in material processing, reagent formulation, technical manufacturing, and in-process and/or final quality control of reagents for use as components of in-vitro diagnostic (IVD) products. Specifically, he/she is involved in bioconjugation, protein purification, and analytical characterization of complex bioconjugates as they relate to the development of tissue diagnostic products for cancer and infectious disease. This position requires the person to adhere to all current industry standard regulations. | 9/20/2022 |
| 6057 | Biocoat Horsham, PA Coating Development Engineer Bachelor of Science in Chemical Engineering, Biomedical Engineering, Mechanical Engineering, or other related engineering field. Exp: 1 year |
Biocoat is a global leader in developing, manufacturing, and applying hydrophilic coatings to medical devices. The team needs an Engineer who would be responsible for developing coating processes and formulations for customer’s devices as well as optimize coating parameters. | 9/20/2022 |
| 6058 | Biocoat Horsham, PA Research and Development Technician B.S. in Chemistry, Biochemistry, or similar focus. Exp: 1-3 years |
Biocoat is the global leader in developing, manufacturing, and applying coatings on medical devices. We are looking for a dynamic and dedicated full-time Research and Development Technician! | 9/20/2022 |
| 6059 | Biomere Richmond, CA Research Associate (Small & Large Animal) BS Degree in Science (or equivalent degree) preferred. Exp: Research Associate I: 1 or 2 years |
Research Associate works under the direct guidance of the Site Head and the general guidance of the senior staff. Research Associate is proficient in animal procedures/animal husbandry, grant, internal, and/or contract research studies according to the study protocols and to the company guidelines and standard operating procedures (SOPs). | 9/20/2022 |
| 6060 | PSC Biotech Durham, NC Junior CSV Engineer Degree or Certification in Engineering Exp: 1-3 years |
We are hiring junior-level CSV Engineers to support Rockwell Automation and Process Control systems. The CSV Engineer is responsible for performing Computer Systems Validation of a PLC Rockwell for a GMP manufacturing process including qualification protocol development (IOQ) and execution. | 9/21/2022 |
| 6061 | PSC Biotech Philadelphia, PA Junior CSV Engineer Degree or Certification in Engineering Exp: 1-3 years |
We are hiring junior-level CSV Engineers to support Rockwell Automation and Process Control systems. The CSV Engineer is responsible for performing Computer Systems Validation of a PLC Rockwell for a GMP manufacturing process including qualification protocol development (IOQ) and execution. | 9/21/2022 |
| 6062 | PSC Biotech Newark, NJ Junior CSV Engineer Degree or Certification in Engineering Exp: 1-3 years |
We are hiring junior-level CSV Engineers to support Rockwell Automation and Process Control systems. The CSV Engineer is responsible for performing Computer Systems Validation of a PLC Rockwell for a GMP manufacturing process including qualification protocol development (IOQ) and execution. | 9/21/2022 |
| 6063 | PSC Biotech Thousand Oaks, CA Mechanical/Project Engineer Bachelor Degree in Engineering Exp: 1-3 years |
We are hiring a Mechanical/Project Engineer to assist the assessment of pressure safety devices. This position is full-time and on-site in Thousand Oaks. | 9/21/2022 |
| 6064 | Blue Rock Therapeutics Toronto, ON Research Associate, Formulation Development Masters degree in Biomedical, Chemical, Material, Biological or Pharmaceutical Sciences or Engineering Exp: 0-3 years |
We are seeking individuals who are collaborative, thrive in a fun and dynamic culture, and are steadfast in the commitment to advance cutting-edge cellular therapies to impact patients’ lives. As part of BlueRock Therapeutics’ vision to change the future of medicine by enabling ground-breaking cell therapies, the candidate will be a key technical contributor of a dynamic and innovative team developing formulations for cellular medicines. The successful candidate will support development of cellular drug product formulations at BlueRock by identifying, designing and testing formulations to optimize cellular drug product in-use stability, cell dose delivery, and cell persistence after transplantation. The ideal candidate will be a highly motivated individual who has demonstrated strong bench skills, excellent documentation skills, attention to detail and enjoys working in a highly cross-functional environment. | 9/21/2022 |
| 6065 | Blue Rock Therapeutics New York City, NY Research Associate I-II, PSC Biology and Differentiation Bachelor’s degree or MSc. preferred field of study includes, but not limited to, biomedical sciences, stem cell biology, bioengineering, biochemistry. Exp: BS: 0-5 years; MSc.: 0-3 years |
We are seeking individuals who are collaborative, thrive in a fun and dynamic culture, and are steadfast in the commitment to advance cutting-edge cellular therapies to impact patients’ lives. The New York, USA site is seeking an RA I-II PSC Biology and differentiation. The ideal candidate will join a team that spearheads our technological and innovative advancement of pluripotent stem cell (PSC) biology, characterization, and production. The individual will plan and execute experiments, keep meticulous records of experimental details, analyze, and interpret datasets. The ideal candidate will enjoy a unique career development environment by interacting with several teams across R&D and manufacturing. The candidate will work closely with scientists from platform and cell biology teams and develop scientific skillsets. | 9/21/2022 |
| 6066 | Blue Rock Therapeutics New York City, NY Research Associate I/II, Genome Engineering B.Sc. or M.Sc. in cell biology, molecular biology, genetics or related discipline Exp: BS: 0-5 years; MSc.: 0-3 years |
We are seeking individuals who are collaborative, thrive in a fun and dynamic culture, and are steadfast in the commitment to advance cutting-edge cellular therapies to impact patients’ lives. The New York, USA site is seeking a Research Associate I or II for the Genome Engineering pipeline that will be reporting to the team lead. The incumbent will be a technical contributor in a dynamic and progressive team pioneering the generation of genome-modified therapeutic cells from human pluripotent stem cells (hPSCs). The individual will participate in the execution of a variety of genetic modifications that enhance cellular properties by employing various gene editing technologies including homologous recombination and CRISPR/Cas to establish cell lines for BlueRock’s research pipeline. The individual will also perform directed differentiation of engineered hPSC lines to determine whether these genome alterations provide BlueRock authentic cell types with novel morphology or function for the replacement of cells that have been damaged or lost to disease. | 9/21/2022 |
| 6067 | Blue Rock Therapeutics New York City, NY Research Associate I, Translational Neuroscience B.S. in Cell Biology, Molecular Biology, Neuroscience, or related discipline Exp: 0-2 years |
BlueRock Therapeutics is seeking a Research Associate I, Translational Neuroscience, based at our New York City location, reporting to the team lead and working closely with colleagues on the team. The incumbent will be a technical contributor on a team responsible for the generation and characterization of pluripotent stem cell derivatives. They will participate in efforts to maintain and characterize pluripotent stem cell (hPSC) cultures, as well as to leverage PSCs for diverse studies of directed differentiation and maturation of specified cell types. Hands-on experience in mammalian cell culture is essential. Experience with human pluripotent stem cells, directed differentiation, cell-based assays, primary cell culture, and/or neurobiology is a plus. The incumbent will work closely with several collaborating teams. This is an outstanding opportunity for a talented individual to contribute to bringing a new class of medicines to patients and gain valuable career experience in the cell therapy space. Collaboration with a highly motivated, world-class team of scientists and engineers promises an exciting and engaging work environment for motivated candidates. | 9/21/2022 |
| 6068 | Blue Rock Therapeutics Toronto, ON Research Associate I, Process Development Bachelors Exp: 0 to 2+ years |
BlueRock Therapeutics is seeking a Research Associate I, Process Development in Toronto, ON. As part of BlueRock's vision to change the future of medicine by enabling ground-breaking cell therapies, the successful candidate will be a key technical contributor to a dynamic and progressive team focused on developing novel therapeutics. The Research Associate II will be involved in hands-on work in developing and scaling cell and gene therapy manufacturing processes | 9/21/2022 |
| 6069 | Boston Analytical Salem, NH Analytical Chemist Bachelor’s degree in Chemistry or a related science discipline is required Exp: 0-2 years |
The Analytical Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. | 9/21/2022 |
| 6070 | Boston Analytical Salem, NH E&L Chemist I Bachelor’s degree in Chemistry or a related science discipline is required Exp: 0-2 years |
The Analytical Chemist conducts routine quantitative and qualitative analyses for Extractables & Leachables studies according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of extracts and pharmaceutical product samples using LC-MS, GC-MS, and/or ICP-MS. | 9/21/2022 |
| 6071 | Boston Analytical Salem, NH Microbiologist - QC BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The QC Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. The schedule for this position is 1:00pm-11:30pm, Monday through Thursday. | 9/21/2022 |
| 6072 | Boston Analytical Salem, NH Microbiologist - Environmental Monitoring BA or BS degree in Microbiology or related science discipline Exp: 0-2 years |
The EM Microbiologist conducts quantitative and qualitative analysis of pharmaceutical industries Environment according to FDA, ISO, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include Sampling of pharmaceutical industries through ISO standards and client specific test protocols. The schedule for this position is 1st shift, Wednesday through Saturday. | 09/21/2022 |
| 6073 | Boston Institute of Biotechnology Southborough, MA Research Associate / Scientist / Sr. Scientist – Downstream Process Development Bachelor’s degree in Biology or Chemistry related field; or MS degree in Biochemistry or Chemical Engineering Exp: BS: 0-10 years; MS: 0-5 years |
Essential requirements for this position include in-depth understanding and hands-on experience with recombinant protein purification from different expression hosts (including E. coli, Yeast, CHO and HEK) and an aptitude for careful, detail-oriented experimentation. The level of the position will be commensurate with the candidate’s experiences. | 09/21/2022 |
| 6074 | Boston Institute of Biotechnology Southborough, MA Upstream Process Development Research Associate BS degree in Biochemical Engineering or related field of study Exp: 0-2 years |
1. Set up, execute, and monitor microbial and mammalian cell culture production in fermenters and bioreactors. 2. Collect, record, and report experimental data. 3. Provide updates to a team lead on a regular basis. 4. Maintain all notebooks and documentation according to department standards. 5. Write SOPs, and batch records. 6. Ability to work well in a team environment and independently as required. | 09/21/2022 |
| 6075 | BostonGene Waltham, MA Research Associate, Molecular Biology and Next Generation Sequencing Bachelor’s (B.S.) degree in biology, clinical laboratory science, medical technology or related discipline Exp: 0-2 years |
BostonGene is seeking a highly motivated Junior Research Associate to join our R&D team in our laboratory located in Waltham, MA. This candidate will support BostonGene’s state-of-the-art primary next generation sequencing (NGS), adjunct analytical platforms, and automated analysis pipelines. The candidate will be expected to develop proficiencies in NGS support protocols, such as RNA and DNA isolation from tissue, cell free DNA isolation from plasma, Whole Exome Sequencing library preparation, RNA-Seq library preparation, qPCR, Molecular Biology techniques, and other sample QC techniques. | 09/21/2022 |
| 6076 | Boston Heart Diagnostics San Diego, CA Research Associate I in vivo Bachelor’s degree in life sciences or related discipline required. Exp: 0-2 years |
The successful candidate for the Research Associate I position will join the Beacon Discovery team with a multifaceted approach for providing high value services based on the Beacon Discovery platform and other proprietary technologies. The position provides an outstanding opportunity to learn new techniques and develop skills within a dynamic in vivo pharmacology research team. We work with multiple animal models, from anxiety to metabolism and beyond. If you are interested in working in a fast paced, challenging environment where you will have an opportunity to learn and succeed this may be the place for you. Laboratory experience with animal handling and pharmacology studies would be advantageous but is not necessary. Extensive training will be provided. | 09/21/2022 |
| 6077 | Boston Heart Diagnostics Foster City, CA HPLC Research Associate Bachelor's/Master’s degree Exp: BS: 0 - 3 years ; MS: 1+ year |
Eurofins Lancaster Laboratories, a nationally recognized laboratory, is searching for HPLC Research Associates to support our Professional Scientific Services group in Foster City, CA. | 09/21/2022 |
| 6078 | Boston Heart Diagnostics San Diego, CA MSAT Research Associate B.S. degree in biological sciences, chemistry, biomedical engineering, immunology, or other related fields Exp: 1-2 years |
This individual will be responsible for performing release, in-process, stability, and process characterization testing for our PSS client’s Cell and Gene Therapy clinical development and commercial programs in a cGMP compliant manner working in the MSAT (Manufacturing Science and Technology) group. This position will perform all activities according to approved written procedures or protocols. Additional responsibilities may include revision to SOPs, method validations, method transfers, and comparability assessments or bridging activities with new analytical methods required for INDa and BLA. | 09/21/2022 |
| 6079 | Boston Heart Diagnostics Cambridge, MA Research Associate, Analytical Development Bachelor’s Degree/ Master’s Degree in related science. Exp: BS: 0-2+ years; MS: 0+ years |
Seeking an energetic and dependable analyst to perform routine testing to support process development and help progress programs through the pipeline. This individual will focus on molecular biology assays with a development opportunity to cross-train and support cell-based, potency, flow cytometry, separations and biophysical methods as well. This analyst will interface with many departments and projects necessary to complete tasks in a timely manner. | 09/21/2022 |
| 6080 | Boston Heart Diagnostics Cambridge, MA Research Associate (Separations + Biophysical) Bachelor’s Degree/ Master’s Degree in related science. Exp: BS: 0-2+ years; MS: 0+ years |
Provide timely internal non-GMP testing support for various teams; Support automation of analytical workflows and qualification of automated assays; Document lab work and results in ELN and/or LIMS; Coordinate, store, and properly handle samples and retains; Manage and track supply of controls, reference standards, and critical reagents; Train other analysts as necessary; Ensure Instruments and lab are properly maintained; Work with many other groups to support client's mission | 09/21/2022 |
| 6081 | PL Developments Copiague, NY Chemist I Chemist I Chemist I Bachelor’s degree in chemistry or related science from an accredited college or university Exp: up to 1 year |
Carry out responsibilities in accordance with the organization’s policies, procedures, and state, federal and local laws. Complies with all current Good Laboratory Practices (cGLP), current Good Manufacturing Practices (cGMP), and safety requirements and laboratory Standard Operating Practices (SOPs). Conduct scheduled preventive maintenance and calibration of laboratory instrumentation (i.e., pH meter, HPLC, dissolution equipment, etc.). Prepare standard and sample solutions as required by the test methods. Operate general analytical instruments for all routine testing (i.e., HPLC, GC, UV, automatic titrator, and IR). Perform wet chemistry tests (i.e., LOD, pH, titration, etc.). | 9/13/2022 |
| 6082 | The Ritedose Corporation Columbia, SC Microbiologist I BS degree in Microbiology or related field Exp: 0 - 2 years |
The Microbiologist I is responsible for all duties related to performing environmental monitoring, personnel monitoring, microbial enumeration, microbial identification, media growth promotion, maintenance of microbial cultures, and sampling of utilities. The Microbiologist I is also responsible for performing all the microbiological testing related to raw materials, utilities, and in-process product testing. Other responsibilities include data entry, data review, ensuring calibration of equipment, maintaining inventory of laboratory supplies, and maintaining the Microbiology laboratory by ensuring its cleanliness and order. | 9/13/2022 |
| 6083 | Tanvex BioPharma San Diego, CA Research Associate, Cell Culture PPD - #1358 BS or advanced degree in chemical/biochemical engineering, cell biology, biochemistry, or related scientific discipline. Exp: 0-3 years |
The Research Associate, Cell Culture Development is responsible for executing individual experiments related to all aspects of cell culture process development of biopharmaceuticals, including media preparation, bioreactor setup, cleaning, sterility and operation, maintaining instruments and equipment, examining data and preparing experiment reports. Applies basic engineering and scientific principles to perform trouble-shooting of processes, instrumentation, and equipment. | 9/14/2022 |
| 6084 | Tanvex BioPharma San Diego, CA Research Associate, Analytical Characterization - #1390 BS or advanced degree in analytical chemistry, chemical/biochemical engineering, biochemistry, or related disciplines. Exp: 0-3 years |
The Research Associate is a key member of the Analytical Characterization team and will be involved in supporting Tanvex’s CMC activities. The ideal candidate will have shown proficiency in hands-on analytical work and strong working knowledge in various physicochemical analyses for detailed characterization of recombinant protein therapeutics. Under the guidance of his/her supervisor, the candidate will help to develop and qualify analytical methods, and conduct characterization analysis to support regulatory filings, as well as provide analytical support for process development and method transfer activities. The candidate is also expected to be involved in drafting characterization study reports, Standard Operating Procedures, method development reports, method qualification protocols and reports, as well as to collaborate with other functional groups on significant technical matters. | 9/14/2022 |
| 6085 | Tanvex BioPharma San Diego, CA Research Associate, Analytical Chemistry Development - #1414 BS or advanced degree in chemical/biochemical engineering, biochemistry, or related scientific discipline. Exp: 0-3 years |
The Research Associate, Analytical Chemistry Development is responsible for providing analytical chemistry support to research, process development, product development and manufacturing of biological therapeutics. Participate in analytical method development, characterization, qualification, validation as well as method transfer. Perform various analysis for characterization of biological therapeutics. | 9/15/2022 |
| 6086 | Tanvex BioPharma San Diego, CA QC Associate, Lab Control & Raw Material - #1346 Bachelor’s degree or advanced degree in chemistry, biology, biochemistry or related life sciences discipline Exp: 0-3 years’ |
The Quality Control Associate, Lab Control & Raw Materials is responsible for conducting routine and non-routine analyses of raw material and GMP product as assigned using appropriate analytical methods. This position will coordinate sampling, shipping, and testing of raw materials at outside contract laboratory and in-house to ensure data integrity and compliance, and will work with internal departments to ensure timely testing of raw materials for Manufacturing. The QC Associate will also perform assay transfers, validation of analytical methods, and testing product GMP samples as assigned, compile data for documentation of test procedures and preparation of reports, and ensure raw materials program is in compliance per internal SOP and CFRs. Knowledge of Laboratory Information Management System (LIMS) is a must. | 9/15/2022 |
| 6087 | Tanvex BioPharma San Diego, CA QC Associate, Validation and Tech Support - #1422 BS or advanced degree in chemistry, biology, biochemistry or related life sciences discipline. Exp: 0-3 years |
The Quality Control Associate, Validation and Tech Support is responsible for supporting the scheduling and maintenance of instruments and equipment in Quality Control. Additional responsibilities include assisting with transferring analytical test methods from development into the QC laboratory, performing feasibility studies, and executing method validations as well as conducting routine and non-routine analyses of GMP products as assigned by the manager. | 9/15/2022 |
| 6088 | Tanvex BioPharma San Diego, CA QC Associate, Lab Control and Raw Materials - #1355 BS or advanced degree in chemistry, biology, biochemistry or related life sciences discipline. Exp: 0-3 years’ |
The Quality Control Associate, Lab Control & Raw Materials is responsible for coordinating sampling, shipping, and testing of raw materials and products at outside contract laboratories and in-house. Additional responsibilities include updating compendial testing requirements (e.g. USP) of raw materials. Work with outside contract labs to ensure data integrity and compliance. Work with internal customers (e.g. Material Management) to ensure timely testing of raw materials for Manufacturing. Knowledge of Laboratory Information Management System (LIMS) is a must. | 9/15/2022 |
| 6089 | Advanced BioScience Labs Rockville, MD QC Microbiology I - (00325_COMPANY_1.4) B.A. or B.S. degree in microbiology, biology, or related scientific field Exp: 1-2 years |
The QC Microbiologist I will have several responsibilities in the QC group. The analyst will perform environmental monitoring (EM) for particulates and viables in support of cGMP manufacturing which includes several production suites of ISO class 5, 7, and 8 as well as EU Grade A to D in a GMP facility that produces biopharmaceuticals (vaccines, biologics, viral vaccines, monoclonal antibodies, etc.). In addition, monitoring of purified water, and compressed gases systems is required. Additional responsibilities may include EM data review and compilation of data, report writing, and trending of data; investigations, gowning training, and annual gowning qualification. | 9/15/2022 |
| 6090 | Advanced Cell Diagnostics Minneapolis, MN Research Associate, Microbiology QC Bachelor’s degree in Microbiology or a related scientific field or equivalent Exp: up to 3 years |
The responsibilities of this position are to participate in the Microbiology QC testing and reporting procedures: set up, read, and report the microbial QC bioburden and sterility testing of various sample types using culture methods that include direct plating, broth inoculation, and membrane filtration. Performance of environmental monitoring for viable microbes, particle counts, and WFI/deionized water testing, reading, and reporting. Assist with efficacy and validation testing, new procedure development, new equipment IQ/OQ and calibrations. Perform general lab duties, assist with sanitization of clean rooms, and additional duties as assigned. | 9/15/2022 |
| 6091 | Advanced Cell Diagnostics Minneapolis, MN Research Associate, Protein Development, Bioassay Bachelor’s degree in a related field Exp: up to 5 years |
We seek a highly motivated and creative individual to join our bioassay development team. This position is responsible for performing and developing bioassays using cytokines and antibodies to evaluate biological activity and to ensure quality products. The position requires maintenance of cell lines and isolation of primary cells for use in the assays. Participate in other projects and troubleshooting as needed. Perform additional duties as assigned. | 9/15/2022 |
| 6092 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate, QC Analyst Masters in Biochemistry, Chemistry, Biology, or a related field. Exp: 0 – 2 years |
Perform routine quality control testing of protein, peptide or antibody products using standard operating procedures to determine lot status, product release and product stability. Tests include: concentration determination, SDS-PAGE with densitometry, SEC/HPLC, endotoxin assay, TOC, conductivity, pH, and other testing as assigned. Participation in the validation of new and existing laboratory methods is also expected. The position requires routine documentation, analysis and communication of results within the department and across different groups. Other duties include instrument calibration and maintenance, record keeping, and lab support. Within this job function, the Research Associate must also pursue annual goals that aim to facilitate innovation, efficiency, productivity, and team building across the QC Department or the entire company. Perform additional duties as assigned. | 9/15/2022 |
| 6093 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate Master’s degree in a related field Exp: up to 2 years |
This position is responsible for participating in the development of Bio-Techne's various product lines. You will maintain knowledge of multiple products and procedures as well as draft and revise standard operating procedures in order to further the ongoing development of new and existing products to help advance Bio-Techne's evolving portfolio. | 9/15/2022 |
| 6094 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate, Bioassay Protein Development Master’s degree in a related field Exp: up to 2 years |
We seek a highly motivated and creative individual to join our bioassay development team. This position is responsible for performing and developing bioassays using cytokines and antibodies to evaluate biological activity and to ensure quality products. The position requires maintenance of cell lines and isolation of primary cells for use in the assays. Participate in other projects and troubleshooting as needed. Perform additional duties as assigned. | 9/15/2022 |
| 6095 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate, Molecular Biology Master’s degree in a related field Exp: up to 2 years |
The responsibilities of this position are to assist the protein product development team in the area of recombinant protein expression. This involves the preparation of expression vectors, cell culture, and screening procedures. The position involves various techniques such recombinant DNA cloning, DNA preparation, high-throughput screening, and DNA sequence analysis. It will also include developing new data processing and analysis tools to further enhance our capabilities and platforms. This is an exciting time to join the Protein Development team at Bio-Techne. This position offers a unique opportunity to work hands on in developing cutting-edge technologies and instrumentation. | 9/15/2022 |
| 6096 | Acessa Health San Diego, CA Research Associate 2 M.S. Molecular Biology, Chemistry, Biochemistry or related field. Exp: 1 year |
Hologic is seeking a Research Associate 2 responsible for automated synthesis of oligonucleotides, purification of oligonucleotides by chromatographic and gel electrophoretic techniques, and characterization of oligonucleotides by a variety of physicochemical techniques. The Research Associate will also participate in basic research projects exploiting novel properties of oligonucleotides in diagnostic assays. This position will also be expected to maintain accurate records of oligonucleotide synthesis and to design and interpret experiments related to the use of novel oligonucleotides in diagnostic assays. | 9/15/2022 |
| 6097 | Agena Bioscience San Diego, CA Research Associate II - Assays by Agena Bachelor’s degree in biology, chemistry or related Exp: 1-3 years’ |
The Research Associate II position is a laboratory-based role. It is part of the Assays by Agena (AbA) team, and under the direct supervision of a Scientist. In this role, you will work on custom assay development for multiplexed panels for detection on Agena Bioscience’s MassARRAY® platform. | 9/15/2022 |
| 6098 | Agenus Berkeley, CA Process Development Research Associate Bachelor’s degree or native equivalent in Biochemistry, Biology, Biotechnology, Cell Biology, Chemistry, Chemical Engineering or a related field Exp: 0-2+ years |
This position will primarily focus on conducting CHO cell culture evaluation and process development in shake flasks and bench scale bioreactors. The successful candidate will be involved in upstream process development of our pipeline programs, including clone evaluation, process parameter optimization, and generation of material to support downstream and analytical development. Strong aseptic techniques and laboratory skills and experience in mammalian cell culture procedures is preferred. Will require some weekend/off-shift work, as needed. | 9/15/2022 |
| 6099 | Agenus Lexington, MA Research Associate - Research & Discovery BS or MS degree in immunology, molecular and cell biology, or related discipline Exp: 1+ years |
Agenus (Lexington, MA) is looking for a talented and highly motivated Research Associate to join our Biomarkers group. The successful candidate is expected to contribute to the discovery, research, and development of novel immunotherapeutic agents to address unmet medical needs of cancer patients. She/he will have opportunities to grow their career through acquisition of new skills, experiences, and professional relationships in a fast-paced and resource-rich environment. Our collaborative and interdisciplinary research team has a track-record of applying state-of-the-art technologies and innovative methodologies to advance cutting-edge immune-oncology (IO) medicines into the clinic. | 9/15/2022 |
| 6100 | Ajinomoto Bio-Pharma Services San Diego, CA Microbiology Technician - 1st Shift Bachelors degree preferred in a Life Sciences discipline or equivalent. Exp: Zero to two (0-2) years |
We are currently seeking an Microbiology Technician to support Ajinomoto Bio-Pharma Services manufacturing. This is a vital role within our Quality Control group and is responsible for supporting manufacturing through collection and testing of water, surface and utility samples during various manufacturing and lab processes. As an Environmental Monitoring Assistant you will acquire an understanding of aseptic technique, continuously exhibit proper clean room behavior, and adhere to cGMPs. | 9/15/2022 |
| 6101 | Ajinomoto Bio-Pharma Services San Diego, CA Microbiology Technician - 2nd Shift Bachelors degree preferred in a Life Sciences discipline or equivalent. Exp: Zero to two (0-2) years |
We are currently seeking an Microbiology Technician to support Ajinomoto Bio-Pharma Services manufacturing. This is a vital role within our Quality Control group and is responsible for supporting manufacturing through collection and testing of water, surface and utility samples during various manufacturing and lab processes. As an Environmental Monitoring Assistant you will acquire an understanding of aseptic technique, continuously exhibit proper clean room behavior, and adhere to cGMPs. | 9/15/2022 |
| 6102 | Alexion Pharmaceuticals New Haven, CT Engineer I, Device Development Bachelor’s degree in Engineering (Biomedical, Chemical, Mechanical, or Electrical Engineering) Exp: 1 to 3 year |
This position will serve the role of Engineer I for device development of Alexion products including continuous product improvement within the Development function of Alexion. The candidate will support technical design and development activities for device and combination products and assist the technology transfer. | 9/15/2022 |
| 6103 | Alexion Pharmaceuticals New Haven, CT Associate Scientist II, Injectable Drug Product Development MS in Pharmaceutical Sciences, Chemistry, Biochemistry, Biophysics, Chemical engineering, or relevant field. Exp: 0 to 1 years |
The position is required to join Injectable Drug Product Development group of Alexion-AstraZeneca Rare Disease pharmaceuticals’ Pharmaceutical Development and Clinical Supply (PDCS) department. The job entails experimental work on various aspects of drug product characterization, including formulation development, in use compatibility studies for intravenous and subcutaneous administration, process development to support drug product manufacturing support, and particulates testing. The position entails execution of the studies and data processing and compiling to generate and support development reports as well as other required documentation. Solid understanding of assay development and bioprocess is highly preferred. Hands-on experience with biotherapeutics development, including detailed understanding product lifecycle, and current regulations for product administration, is highly desirable. In addition, this position is expected to interact regularly with scientific staff within the department and in some cases with colleagues in other departments (e.g., Analytical Sciences, Device development, Biologics Drug Substance Process Development) The ability to accurately and independently generate procedures, protocols, reports, and CMC section content for regulatory filings pertaining to drug product is a requirement of this position. | 9/15/2022 |
| 6104 | Alexion Pharmaceuticals New Haven, CT Associate Scientist II, Small Molecule DMPK Master or equivalent degree in chemistry, biochemistry, biology or any other disciplines related to pharmaceutical sciences Exp: 0-2 years |
The Small Molecule Drug Metabolism and Pharmacokinetics (DMPK) team of Alexion, AstraZenica Rare Desease, is seeking an associate scientist to support drug metabolism studies in discovery and early development. | 9/15/2022 |
| 6105 | Alexion Pharmaceuticals New Haven, CT Associate Scientist II, IVIVP MS Exp: 0-2 years |
We are seeking a highly motivated in vivo pharmacologist to work in a dynamic preclinical environment focused on delivering clinically translatable solutions to advancing drug development. The full-time role will focus on the design, development, and evaluation of lead therapeutics in nonclinical pharmacology studies and ex vivo biochemical and bioanalytical assays support. The successful candidate will contribute to development and characterization of in vivo mouse models, as well as support ex vivo protein and cellular analysis. | 9/15/2022 |
| 6106 | American Regent New Albany, OH R&D Analytical Chemist R&D Analytical Chemist B.S. in Chemistry or equivalent education required. Exp: 1 year |
This R&D position will be responsible for testing of raw materials, finished products, and stability samples using existing analytical methods and wet chemistry. | 9/16/2022 |
| 6107 | American Regent New Albany, OH Validation Engineer I Validation Engineer I Bachelor’s Degree in Life Sciences, Engineering or equivalent required. Exp: 1 year |
The Validation Engineer I will develop and execute validation protocols and reports that support the business needs of the company. The position will support the qualification and validation of the pharmaceutical manufacturing processes and ensure that the facility, systems and processes perform according to internal specifications, comply with current GMPs and are maintained in a validated state. | 9/16/2022 |
| 6108 | Ampac Analytical Rancho Cordova, CA Quality Chemist I Bachelor’s degree in Chemistry or an appropriate science required. Bachelor’s degree in Chemistry or an appropriate science required. Exp: One (1) to two (2) years |
Must use independent judgment to analyze and make determinations as to the quality of a product, using analytical equipment pertinent to the appropriate application of skills. Use various laboratory procedures related to analysis of bulk and pharmaceutical chemicals. Perform analysis of samples using various laboratory equipment and techniques such as FT-IR, Loss On Drying, Non-volatile Residue, Titrations, moisture analysis by Karl Fischer, in addition to other methods. Operate LC and GC systems in order to complete analyses of various types of samples. Maintain a thorough and neat laboratory notebook. Troubleshoot fixes for various instruments in the laboratory. May perform peer review of various commercial product laboratory data. | 9/16/2022 |
| 6109 | Ampac Analytical Rancho Cordova, CA Process Engineer Bachelor's of Science Degree in Chemical Engineering required. Exp: One to three years |
We are looking for enthusiastic Chemical Engineers to join our Process Engineering Team! We have several opportunities at our Rancho Cordova, CA location (Greater Sacramento Area). We will pay for your relocation!! | 9/16/2022 |
| 6110 | Ansa Biotechnologies Emeryville, CA Research Associate / Senior Research Associate, Downstream Process Development Bachelor’s/Master’s Exp: 0-4 years |
Execute downstream processing workflow for recombinant protein production: E. coli harvest, lysis, clarification, purification, and buffer production Keep detailed notes of experimental procedures and observations using an electronic lab notebook Collaborating in a team environment: At Ansa, communication between teams is critical–our technology is built on enzymes, chemistry, and automation. Additionally, we believe that kind-natured honesty and openness are an instrumental part of the scientific endeavor. | 9/16/2022 |
| 6111 | Arbor Biotechnologies Cambridge, MA RA/SRA, Protein Engineering Bachelor’s degree in molecular biology, biochemistry, or a related field Exp: 1-3 years |
The Protein Engineering Team is looking for a RA/SRA to join our cross-functional team and contribute to the discovery and development of novel gene editing systems. This role affords the opportunity to hone molecular biology techniques and help develop new assays and methods in a fast-paced environment all while making a broad impact on Arbor’s productivity and portfolio. The ideal candidate will have hands-on experience in the wet laboratory, an appetite for learning a wide variety of topics, excellent organizational skills, attention to details, and the ability and self-motivation to work independently. | 9/16/2022 |
| 6112 | Arbor Biotechnologies Cambridge, MA Research Associate/Senior Research Associate, Non-Viral Gene Therapy BS/MS or equivalent in Chemical/Biomedical/Biochemical Engineering, Bioengineering, Chemistry, Biochemistry, Pharmaceutical Sciences or a related fiel Exp: 1-3 years |
The Senior Research Associate/Research Associate will support our LNP formulation pipelines and in vitro/in vivo preclinical requirements through the design and execution of experiments to help screen and produce various non-viral formulations enabling the encapsulation of various RNA entities. This candidate will also help support various characterization assays for the various formulations as needed. The ideal candidate for this position will be a motivated and proactive individual with a passion for nanomedicinal/LNP formulations and processes. The applicant should have strong wet laboratory, communication and collaboration skills preferably with a background in the appropriate formulation deliverables. This role will have no supervisory responsibilities and will report to the Principal Scientist, Non-Viral Gene Therapy. | 9/16/2022 |
| 6113 | ArcherDx San Francisco, CA Clinical Laboratory Technician - Tissue Culture BS in Cell Biology, Molecular Biology, Biochemistry, or equivalent Exp: 1+ years |
We are looking for a versatile, detail oriented Tissue Culture Technologist to join our San Francisco laboratory who can, with minimum supervision, perform cell culturing and microscopic analysis. | 9/16/2022 |
| 6114 | ArcherDx San Francisco, CA DNA Extraction Technician Bachelor’s degree in clinical laboratory studies or equivalent science related studies Exp: 1+ years |
We're looking for passionate laboratory technicians who will support high complexity laboratory testing on patient specimens across various assays and platforms. This role will be performing quality control and quality assurance procedures while complying with all applicable local, state and federal laboratory requirements. The work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask and be flexible with tasks and schedules, and the ability to work independently in a team environment. This role requires on-site work at our San Francisco location as well as ability to work overtime and off-schedule days as needed. | 9/16/2022 |
| 6115 | ArcherDx San Francisco, CA Engineering Technician Bachelor degree in an engineering or science field preferred Exp: 1 – 2 years |
We are looking for a passionate and driven Engineering Technician to join our Equipment Engineering Team who can come in and own the day to day equipment tasks which maintain regulatory compliance, equipment states and a high functioning lab environment. This individual will be able to seamlessly interface with production and engineering teams to drive forward task completion. | 9/16/2022 |
| 6116 | ArcherDx Iselin, NJ Extraction Technician Bachelor’s or Master's degree in Medical Technology, Biology, Chemistry, Biochemistry or related life science Exp: 1 years |
Our Iselin (Metropark), NJ operations team is looking for a passionate and focused Extraction Laboratory Technician I to join invitae and support high-complexity laboratory testing on patient specimens across various assays and platforms. The extraction team member will partner with the Extractions Lead to continuously improve daily extraction operations at our Metropark Laboratory. | 9/16/2022 |
| 6117 | ArcherDx San Francisco, CA Clinical Laboratory Scientists - I, II, III, or IV Bachelor's degree in clinical laboratory studies or equivalent science related studies. Possess an active, valid license (Generalist or CGMBS) issued Exp: 1+ years |
We are looking for a motivated and self-driven Clinical Laboratory Scientist to join our team. This role will be responsible for performing high complexity diagnostic testing on patient specimens across various molecular assays and platforms (Including NGS, NIPS, aCGH, MLPA, ddPCR, Genotyping, Sanger and Long Range Sequencing). This role envelopes all steps from specimen processing to data analysis; performing quality control and assurance procedures, while complying with all applicable local, state and federal laboratory requirements. The work requires excellent attention to detail, strong written and verbal communication skills, and the ability to multitask as well as work independently within a team environment. | 9/16/2022 |
| 6118 | Arcturus Therapeutics San Diego, CA Research Associate I/II MS/BS degree in biochemistry, biological sciences, pharmaceutical sciences, chemistry, chemical engineering, molecular biology, or other relevant disc Exp: 1 to 5 years |
Arcturus is seeking a Research Associate to join our RNA team. This individual will work with a team of highly-motivated scientists to advance development projects within RNA production, RNA process development, RNA formulations, and analytical sciences. | 9/16/2022 |
| 6119 | Arcturus Therapeutics San Diego, CA Research Assistant/Research Associate I, Analytical Development Bachelor’s degree in Chemistry, Biochemistry, Molecular Biology, Pharmaceutical, Life Science or equivalent. Exp: Zero to two (0-2) years |
The Research Associate, Analytical Development will be responsible for conducting routine analytical characterization of RNA drug substances, intermediates and formulated drug products to support an emerging research pipeline focused on treating rare diseases. The candidate will also assist with optimization, development and implementation of new analytical procedures as needed. | 9/16/2022 |
| 6120 | Arrowhead Pharmaceuticals San Diego, CA Research Associate, Biology (In Vitro) BS in Biology, Physiology, Pharmacology, or relevant area Exp: 0-2 years |
Arrowhead is seeking a Research Associate to join our growing Biology Department at San Diego site. This is an excellent opportunity to utilize, contribute and advance the ideal candidate’s laboratory skills in a progressive, state-of-the-art and diverse facility. | 9/16/2022 |
| 6121 | Xencor Monrovia, CA Research Associate 1 Research Associate 1 Research Associate 1 Bachelor’s degree in biological sciences, cell biology, immunology or a related field is preferred. Exp: 1 years |
Responsible for contributing to daily laboratory operations in support of the identification of therapeutic antibody candidates using specialized methods specific to the assigned group, function or department. | 9/6/2022 |
| 6122 | Xencor Monrovia, CA Research Associate 1 BS in cell biology, immunology or related field; MS is highly preferred. Exp: 1 year |
We currently have an excellent opportunity for a talented Research Associate 1 to join our team! Job Duties Include: Grow and maintain mammalian cell lines Mammalian protein expression and plasmid DNA purification Performs primary mammalian tissue culture Maintains tissue cultures including mammalian primary cells and cell lines Coordinate and collaborate tasks across multiple groups, aligning with molecular biology and protein purification Documents experimental protocols, designs, and results in a laboratory notebook Employs computer programs to collect and analyze data Performs other duties as required | 9/6/2022 |
| 6123 | Zymo Research Irvine, CA Bioinformatics Associate Master or bachelor's degree in Biology, Bioinformatics, Computer Science, Mathematics, Statistics, or a related discipline. Exp: 1 to 3 or more years |
Zymo Research is seeking a Bioinformatics Associate to join our Bioinformatics team. The qualified individual will play a key role in building, maintaining, and executing data-analysis pipelines for Next-Generation Sequencing methods to support Zymo Research’s global product strategy. If you are passionate about helping people in advancing science and working with awesome teams in a fast-growing company, we want you | 9/7/2022 |
| 6124 | Zymo Research Irvine, CA Research Associate – Protein Engineering Group MS degree or a BS Exp: one-year |
Zymo Research is seeking highly motivated individuals to join our R&D team as Research Associate. The qualified individual will lead and execute R&D projects for product development, optimization, and quality control. You will be working closely with some of the most talented people in the life sciences field, developing recombinant proteins and peptides production methods. If you are passionate about helping people in advancing science and working with awesome teams in a fast-growing company, we want you! | 9/7/2022 |
| 6125 | Zymo Research Irvine, CA Research Associate MS degree or a BS Exp: one-year |
Zymo Research is seeking highly motivated individuals to join our R&D team as Research Associate. The qualified individual will lead and execute R&D projects for product development, optimization, and quality control. You will be working closely with some of the most talented people in the life sciences field, developing recombinant proteins and peptides production methods. If you are passionate about helping people in advancing science and working with awesome teams in a fast-growing company, we want you! | 9/7/2022 |
| 6126 | Zymo Research Irvine, CA Research Associate – Assay Development MS degree or a BS Exp: one-year |
Zymo Research is seeking highly motivated individuals to join our R&D team as Research Associate. The qualified individual will lead and execute R&D projects for product development, optimization, and quality control. You will be working closely with some of the most talented people in the life sciences field. If you are passionate about helping people in advancing science and working with awesome teams in a fast-growing company, we want you! | 9/7/2022 |
| 6127 | Zymo Research Irvine, CA Research Associate (RNA Seq team) MS degree or a BS Exp: one-year |
Zymo Research is seeking highly motivated individuals to join our R&D team as Research Associate. The qualified individual will lead and execute R&D projects for product development, optimization, and quality control. You will be working closely with some of the most talented people in the life sciences field specifically in the cutting-edge technologies of next-generation sequencing (NGS) and nucleic acids handling. If you are passionate about helping people in advancing science and working with awesome teams in a fast-growing company, we want you! | 9/7/2022 |
| 6128 | Zymo Research Tustin, CA Laboratory Technician/QC Associate BS degree in Biochemistry, Microbiology, Genetics, Immunology, Virology, Molecular Biology or related field. Exp: 1-2 years |
Assist in the manufacturing of various chemicals, buffers, and other product-related components to ensure consistent product performance. Responsible for conducting quality control tests on various chemicals, buffers, and other product-related components. | 9/7/2022 |
| 6129 | Accelerate Diagnostics Tucson, AZ Research Associate, Core Lab (2nd Shift) Bachelor of Science degree in Microbiology, Molecular Biology, or related life sciences. Exp: 1 year |
The shift for this position is Monday - Friday, 2:00pm – 11:00pm. The Research Associate is responsible for the routine execution of experiments supporting assay development, technical operations, and core lab. This position can be in different teams including assay development, core lab and technical operations depending upon business needs. | 9/7/2022 |
| 6130 | Affinivax Cambridge, MA QC Analyst 1 - Vaccine Development Bachelor/Master of Science in Biology, Molecular Biology, Biochemistry, Chemistry, Analytical Chemistry Exp: 1+ years |
Affinivax is currently seeking a motivated QC Analyst to join our Quality Control Team to support and contribute to our development efforts and ongoing clinical trial. | 9/8/2022 |
| 6131 | Sciecure Pharma Monmouth Junction, NJ QC & ARD Chemist Bachelor’s degree from four-year college or university in any of the following disciplines: Chemistry, Biology, Microbiology, or related sciences (as Exp: 1 year |
The Analytical R&D laboratory supports, development and validation of methods analytical test methods, evaluation and testing of raw materials, and testing of non-commercial materials to support product development. All activities are performed in accordance with specifications, standard operating procedures, approved test methods and/or protocols, regulatory requirements. | 9/8/2022 |
| 6132 | Sciecure Pharma Monmouth Junction, NJ Project Coordinator Bachelor’s degree in Life Science (Biology, Chemistry, Chemical Engineering, Etc.). Exp: 1 – 3 years |
Sciecure Pharma Inc. specializes in the research and development of pharmaceutical finished products from conception to commercial. Our growing company is seeking to hire a project coordinator who will be in charge of assisting in organizing our ongoing projects. This task involves monitoring project plans, schedules, organizing and participating in stakeholder meetings, and ensuring that project deadlines are met in a timely manner. To be successful as a project coordinator, you will need to be able to work on tight deadlines, be competent in using Microsoft Office applications such as Word and Excel, and have exceptional verbal, written, and presentation skills. A bachelor’s degree in life science is required for consideration. | 9/8/2022 |
| 6133 | Spriaso Salt Lake City, UT Research Chemists Bachelor's degree in chemistry, chemical engineering, biochemistry, or other related degree concentration Exp: one year |
These positions entails doing product, process, and analytical functions in support of product and technology development under direction of product development and/or analytical leader. | 9/9/2022 |
| 6134 | Tanabe Research San Diego, CA Research Associate I/II – Oncology BS in a biology-related field such as Cell Biology, Molecular Biology, Immunology, Biochemistry, etc. Exp: 0-2 years |
An entry level Research Associate for our Oncology department to conduct biological studies using standard to advanced cell biology and immunological techniques. | 9/9/2022 |
| 6135 | Vaxess Technologies Cambridge, MA Research Associate, Bioassays Bachelor’s or Master’s degree in Life Sciences Exp: 1-2 years |
Research & development at Vaxess is cross-disciplinary, integrating biology, chemistry, immunology, materials sciences, and engineering to address important unmet medical needs in vaccines and therapeutics. We are seeking a talented, collaborative, and highly motivated individual with expertise in bioassays to join our core team of scientists and engineers. This is a unique opportunity to be part of an emerging early phase clinical company bringing innovative technology to the global market. | 9/9/2022 |
| 6136 | Vaxess Technologies Cambridge, MA Research Associate / Senior Research Associate, Formulation and Analytical DevelopmentResearch Associate / Senior Research Associate, Formulation and Master’s degree in one of the Life Sciences, Chemistry, Pharmaceutical Sciences, Chemical Engineering or Biomedical Engineering Master’s degree in one Exp: 0-2+ years |
Research & development at Vaxess is cross-disciplinary, integrating biology, chemistry, immunology, materials sciences, and engineering to address important unmet medical needs in vaccines and therapeutics. We are seeking a talented, collaborative, and highly motivated individual with expertise in formulation and analytical development to join our core team of scientists and engineers. This is a unique opportunity to be part of an emerging early phase clinical company bringing innovative technology to the global market. | 9/9/2022 |
| 6137 | Aesculap Irvine, CA QC Chemistry Associate II (Chemical Chromatography) Bachelor's degree in a Science related field preferred. Exp: 01-02 years |
Perform routine laboratory analysis of In-Process, finished product, raw material, stability samples and environmental monitoring according to established specifications and procedures using wet chemistry techniques or various laboratory apparatus and instruments (e.g. HPLC, UV/Visible Spectrophotometer, FTIR, TOC, pH meter etc.) in compliance with B. Braun, cGMP, GLPs, SOPs, USP and FDA guidelines. | 9/9/2022 |
| 6138 | Aesculap Irvine, CA QC Chemistry Associate II (In Process Chemistry) Bachelor's degree in a Science related field preferred. Exp: 01-02 years |
Perform routine laboratory analysis of In-Process, finished product, raw material, stability samples and environmental monitoring according to established specifications and procedures using wet chemistry techniques or various laboratory apparatus and instruments (e.g. HPLC, UV/Visible Spectrophotometer, FTIR, TOC, pH meter etc.) in compliance with B. Braun, cGMP, GLPs, SOPs, USP and FDA guidelines. | 9/9/2022 |
| 6139 | Aesculap Irvine, CA Quality Operations Associate II Bachelor's degree in a Science related field preferred. Exp: 01 – 02 years |
The Quality Operations Associate II under a moderate degree of supervision is responsible for performing incoming and in-process inspection (visual, functional and dimensional) using qualified instruments. This position will also be responsible for reviewing data, certificate of compliance and performing materials release as required. | 9/9/2022 |
| 6140 | AGC Biologics Longmont, CO QC Associate I/II, Microbiology Degree in Microbiology, biology or other scientific discipline Exp: 0-2+ years |
The Microbiology Associate I/II will be part of the Longmont Quality Control Microbiology Department. This individual will be responsible for the testing and support of the Microbiology Laboratory in support of a cell and gene therapy Contract Manufacturing facility. Responsibilities include routine Quality Control laboratory activities in support of GMP testing, and execution of laboratory maintenance activities. | 9/9/2022 |
| 6141 | AGC Biologics Boulder, CO Manufacturing Associate I-III BS in Chemistry, Biology or other relevant discipline. Exp: 1-7 years |
The Manufacturing Associate I-III performs GMP manufacturing operations safely, reliably and in compliance with stated processes. We offer a dynamic environment, innovation, operational excellence, and career growth. | 9/9/2022 |
| 6142 | Amphastar Pharmaceuticals Inland Empire, CA Microbiologist Bachelor's degree from four-year college or university in biology or related field Exp: one to two years |
A Pharmaceutical Manufacturing company is looking for the talents of a Microbiologist to perform a variety of tests which directly or indirectly affect product release, and test for the sterile quality of products manufactured by performing the following duties. | 9/9/2022 |
| 6143 | Amphastar Pharmaceuticals Rancho Cucamonga, CA In Vitro Bioassay Analyst Bachelor's degree in biochemistry, biology, molecular biology or other related degree concentration (required). MS in biochemistry, biology, molecular Exp: one year |
The in vitro bioassay analyst is an entry level role and will be responsible for assisting in the development and qualification of cell-based potency and ELISA/immunology-based drug products. They will also be responsible for the on-time release and stability of raw materials, in-process, finished pharmaceutical drug substances and drug product and non-routine testing of drug product in a cGMP environment. | 9/9/2022 |
| 6144 | Amphastar Pharmaceuticals Rancho Cucamonga, CA Process Technology Development Engineer Bachelor's degree (Bachelor of Science) from a four-year College or University in Chemical Engineering or other relevant scientific field. Exp: One to two years |
The Process Technology Development Engineer researches and evaluates new technology and design related to new equipment, process scale up and process improvement. Identify critical to quality attributes of the process and perform experiments to study the process control with the aim of optimizing the process at various stages in its product life cycle. Achieves the corporate target and ensure smooth process development and transfer for the commercial scale production. . | 9/9/2022 |
| 6145 | Amphastar Pharmaceuticals Rancho Cucamonga, CA Maintenance Engineer Bachelor's degree (B.S.) from four-year college or university in Mechanical or Electrical engineering or other relevant scientific field. Exp: 6 months |
Perform setup, maintenance and operation of aseptic and non-aseptic production equipment along with general facility repair and maintenance. | 9/9/2022 |
| 6146 | Nitto Denka Avecia Cincinnati , OH Quality Assurance Specialist Quality Assurance Specialist BS/BA in science Exp: 1-3 years |
Acts as departmental resource for cGMP programs Writes SOP’s compliance documents for cGMP program. Reviews and authorizes batch production records and quality control documentation. Performs compliance audits of suppliers, contract labs and vendors then writes audit reports. Performs internal audits and ensures observations are corrected. Sets-up and tracks material flow and material-labeling process to ensure compliance with cGMP program Trains staff in area of cGMP and maintains training records | 9/9/2022 |
| 6147 | Nitto Denka Avecia Milford, MA Quality Control Environmental Analyst I Quality Control Environmental Analyst I BS in chemistry, biology or related discipline or equivalent combination of education and experience Exp: 0-2 years |
Purpose of Position: The QC Environmental Analyst I supports manufacturing operations by performing environmental monitoring of the cleanrooms, and sampling and testing of the water system, as well as perform additional microbial sampling and testing as required. The position works within the QC lab on assigned tasks following written procedures and protocols. The position also assists in the maintenance of overall laboratory systems. | 9/9/2022 |
| 6148 | Nitto Denka Avecia Milford, MA Quality Control Analyst I (2nd Shift) BS in chemistry, biology or related discipline or equivalent combination of education and experience Exp: 0-2 years |
Purpose of Position: The QC Analyst I is responsible for conducting routing analysis of raw materials, in-process samples and finished products in a strict GMP setting. The position involves working in the QC laboratory and in the manufacturing space on assigned tasks following written procedures and verbal instructions. | 9/9/2022 |
| 6149 | Nitto Denka Avecia Milford, MA Research Chemist Research Chemist BA/BS/MS Exp: BA/BS: 1+ yrs.; MS : 0+ yrs. |
The Research Chemist is responsible for meeting the analytical testing requirements to support research and development projects primarily focused on oligonucleotides | 9/9/2022 |
| 6150 | Avidity Biosciences San Diego, CA RESEARCH ASSOCIATE, BIOANALYTICAL BS or MS in Biology, Biochemistry, or related discipline Exp: 1 year |
We are seeking a Research Associate focused on bioanalysis to join the Bioanalysis team at Avidity Biosciences in La Jolla, CA. This position will require hands-on lab work with responsibility for processing and analyzing animal blood and tissues. The ideal candidate will be able to assist in the development of novel methods for quantifying antibodies and oligonucleotides in complex biological matrices. The ideal candidate is expected to be a strong team player who enjoys scientific discovery and can communicate and collaborate in a fast-paced interdisciplinary environment. Title and compensation will be commensurate with the candidate’s experiences. | 9/9/2022 |
| 6151 | Avidity Biosciences La Jolla, CA RESEARCH ASSOCIATE, IMMUNOLOGY B.S./B.A. degree in the biological sciences Exp: 1-2 years |
Avidity is seeking an enthusiastic and dedicated Research Associate to join our Discovery Biology team who can assist with ongoing studies that aim to expand our AOC platform. This is a hands-on research position, and a successful candidate will have a proven record of producing exceptional results in a laboratory setting. | 9/9/2022 |
| 6152 | Bio-Concept Laboratories Boston, MA Associate Scientist I - Boston, MA (Entry Level) Recent Bachelor’s degree in chemistry, biochemistry or related field. Exp: Entry Level |
We are seeking a talented and self-motivated scientist (recent graduate or upcoming graduate) who is eager to be part of our success, and who embraces our core values: Integrity, Excellence, and Teamwork. This role requires scientific curiosity, willingness and eagerness to learn and support drug development efforts. If you have a passion for hands-on problem solving to develop cutting-edge pharmaceuticals, this is the job for you! Working in a dynamic, fast-paced, team-oriented and collaborative environment at Pace Analytical Life Sciences! | 9/9/2022 |
| 6153 | Biomarker Strategies Rockville, MD Technician or Research Assistant (Part-time positions considered) Academic qualifications not listed. Exp: 1+ years |
BioMarker Strategies seeks highly motivated laboratory personnel who will assist in the development of a commercialization-focused cancer diagnostic system. Candidates will be responsible for performing research and development experiments, and to be able to summarize experiments and results. This position is a wet lab position and candidate will predominately perform work at the bench. | 9/9/2022 |
| 6154 | ChemPacific Baltimore, MD Chemist Master’s degree in Chemistry or Organic Chemistry Exp: one year |
Perform multi-step organic synthesis in solution and/or solid support: Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps such as extraction, recrystallization, silica gel column chromatography and LC/MS purification; perform cGMP synthesis of pharmaceutical ingredients; and perform process development and scale-up for kilogram quantities; and clearly record and communicate results and challenges to coworkers/supervisor. Equipments and tolls used included NMR, UV, MS and IR, Reactor (from 50ml to 221 to 10000l), vacuum pump, water aspirator, condenser, rotavap, voltage transformer, chromatography columns, TLC monitor, lyophilizer, separation funnel and addition funnel. Please send your resume to xtan@chempacific.com | 9/9/2022 |
| 6155 | CRISPR Therapeutics San Francisco, CA Research Associate I/II, CRISPRx BS in biology or related discipline Exp: 0-3 years |
We are seeking a Research Associate I/II to join the CRISPRx group at CRISPR Therapeutics, the leading gene editing company. The successful candidate will be an integral part of a team whose aim is to advance next generation gene editing. The position requires enthusiasm, passion, attention to detail and a desire to assist in developing the next generation of gene editing. | 9/9/2022 |
| 6156 | Ferndale Pharma Group Ferndale , MI Microbiologist Bachelor’s degree in Microbiology or a closely related field, or an equivalent combination of education and experience. Exp: One year or more |
Carries out routine day-to-day microbiological testing of Water, Raw Materials, Bulk and Finished Products and Stability samples in the Microbiology Laboratory. Performs routine microbiology testing, such as pour plate methods, membrane filtration, Preservative Effective Testing, and isolation and identification of organisms. | 9/9/2022 |
| 6157 | Ferndale Pharma Group Ferndale , MI Chemist Bachelor of Science in Chemistry or a closely related field or an equivalent combination of education and experience. Exp: one to two years |
Carry out routine day-to-day quality control testing of Water, Raw Materials, Bulk, Finished Products and Stability samples in the Quality Control Laboratory. Perform routine chemical testing by such means as HPLC, GC, FTIR, UV Spectrophotometry, Titrations and other physical and chemical techniques. Review note books and generate test data reports. Write and revise SOPs. Prepare protocols, perform testing for special investigations and write scientific reports. | 9/9/2022 |
| 6158 | Cellular Technology Limited Cleveland, OH Laboratory Assistant Bachelor of Science degree. Exp: one year |
We are seeking a highly motivated Laboratory Assistant for our Contract Research Laboratory who will perform immunology testing of client specimens collected from both pre-clinical and clinical studies using the following test methods: ELISPOT, ELISA, flow cytometry, etc. All work is performed according to general laboratory safety standards, internal standard operating procedures (SOPs), client protocols, and applicable international, federal and state regulations. | 9/9/2022 |
| 6159 | Lampire Biological Labs Pipersville, PA CELL CULTURE TECHNICIAN Bachelor's Degree in a scientific field preferred. Exp: 0-2years |
Scope of Responsibility: To perform cell culture and cell banking activities such as Hybridoma development and growing of monoclonal cells in culture and to document activities accurately at Lampire with the goal of providing consistent, high-quality products and services to our customers with complete, accurate documentation. | 9/9/2022 |
| 6160 | Lampire Biological Labs Pipersville, PA LABORATORY ANIMAL TECHNICIAN Bachelor’s Degree in a scientific field preferred Exp: 0-2years |
Job Description: The project related functions for the small lab animals, including but not limited to mice, rats, guinea pigs, and hamsters. This person will be responsible for preparing and administering injections, performing bleeds, processing bleeds and updating records as needed. To perform animal procedures as the project dictates on small laboratory animals and input data at Lampire with the goal of providing consistent, high quality products and services to our customers with complete, accurate documentation. | 9/9/2022 |
| 6161 | Sofregen Medical Framingham, MA Quality Engineer Bachelor’s degree in scientific discipline Exp: 0-2 years |
Sofregen Medical is seeking a Quality Engineer to join our Manufacturing team and support the production of Sofregen’s commercial silk-based medical device platform. The Quality Engineer plays a vital role in the maintenance of the Quality Management System as well as the daily operation of the laboratory. Duties will include maintaining a system to track equipment calibration & maintenance, environmental monitoring, inventory management, receiving and incoming inspection, and authoring routine Quality Control documentation (e.g. deviations, standard operating procedures (SOPs), batch records, etc.). The Quality Engineer will further collaborate with Manufacturing members to provide general support to critical processes. | 8/29/2022 |
| 6162 | Sound Biologics Bothell, WA ASSOCIATE SCIENTIST/SR. ASSOC. SCIENTIST BS or MS degree in analytical chemistry, biochemistry, chemical engineering, or a similar discipline Exp: 1+ years |
Sound Biologics is seeking analytical development and characterization scientist to participate in the R&D activities from preclinical studies, process development, through GMP production and IND filings. This is a unique opportunity for a motivated scientist to contribute experimentally, as well as intellectually, in advancing our mission in a supportive, but fast-paced team setting. | 8/29/2022 |
| 6163 | Spherotech Lake Forest, IL Quality Control Associate Bachelor's degree in Chemistry or related field Exp: 1 year |
Spherotech, Inc. seeks a college graduate for a Quality Control Associate opening. Duties include final product inspection, documentation, Quality Control testing etc. | 8/29/2022 |
| 6164 | Spotlight Therapeutics Hayward, CA Research Associate (RA) - Protein Engineering BS/MS in Biochemistry, Molecular Biology, Genetics, or related field Exp: 1-2 years |
We are seeking a biochemist/molecular biologist to join our Platform Technology group. Our group is building a new class of biologics from a toolbox of CRISPR/Cas systems, affinity domains, and cytosolic delivery technologies. In this role, the candidate would design novel RNPs and optimize therapeutic properties such as stability and editing efficiency, using both protein and RNA engineering. This position is an outstanding opportunity to contribute directly to our core protein engineering and production capabilities, as well as work directly with our cell biologists, immunologists, and gene editing experts. Primary responsibilities will include several aspects of protein engineering, such as plasmid construct design, protein expression, and purification. In addition, biochemical assays would be carried out to assess purity, concentration, stability, integrity, and enzymatic activity of RNPs. | 8/29/2022 |
| 6165 | Stability Biologics San Antonio, TX QA Specialist - San Antonio, TX BS degree in a scientific discipline (Chemistry, Biology, Physics, Bio-Medical Engineering/Chemical Engineering, etc.) Exp: 1 year |
The Quality Assurance Specialist (QAS) will be a member of the Stability Biologics Quality Dept. to perform quality record reviews, batch release, record retention, data entry, auditing, investigations and document control activities. The QAS will be responsible for quality assurance metrics, CAPA/NCMR and maintaining all quality records/batch records in a secure and controlled manner. The QA Specialist will also be responsible for ensuring all policies and procedures are in compliance with appropriate FDA, AATB, states, and Stability Biologics standard operating procedure. | 8/29/2022 |
| 6166 | StageBio Marlboro, MA Laboratory Imaging Specialist (Preclinical CRO) College degree preferred (in a technical major like electrical, imaging, computer, biomedical engineering) Exp: 1-2 years’ |
StageBio is seeking a full-time Imaging Specialist to join our Marlborough, MA facility. | 8/29/2022 |
| 6167 | StellarTech Research Milpitas, CA Quality Engineer II BS degree or equivalent. Exp: 1-3 years |
Stellartech is looking for a Quality Engineer to join our Team. | 8/29/2022 |
| 6168 | SteriPharma Syracuse, NY Microbiology Analyst, 2nd Shift, Pharma Bachelor’s degree from a regionally accredited institution in science or related field. Exp: 1-3 years’ |
This position performs environmental monitoring and quality control of aseptic process area, to include testing of finished products, raw materials, and components according to established procedures. Position reviews records for accuracy. Position applies standard concepts, practices, and procedures within the laboratory. | 8/29/2022 |
| 6169 | Strand Therapeutics Boston, MA Associate Scientist/Sr Associate Scientist, Bioanalytical M.S. in Biology, Immunology, Biochemistry, Pharmacology, or a related field. Exp: 1-3 years |
Strand’s Bioanalytical Sciences team is looking for a Boston-based Associate Scientist/Sr Associate Scientist with hands-on experience in bioassay development. The individual in this role will support discovery & development programs through the development and execution of bioanalytical assays and by interfacing with internal & external stakeholders. The individual will work with scientists within the Bioanalytical Sciences team, broader Nonclinical group, and other functional groups to ensure that only the highest quality data is generated by our team. The successful candidate must have experience in assay development and specifically hands-on experience executing ELISA (& MSD), Luminex, qPCR/RT-qPCR, flow cytometry and other bioanalytical assays. The candidate must have integrity, be respectful and courteous, have a collaborative spirit, and come ready to make an immediate impact. | 8/30/2022 |
| 6170 | Strand Therapeutics Boston, MA Associate Scientist, mRNA Process Development BS in Biochemistry, Chemical Engineering, Molecular Biology, Bioengineering, Molecular Medicine, Genetics or related field preferred. Exp: 1-2+ years |
We are looking for a highly motivated and innovative candidate for the role of Associate Scientist, mRNA Process Development. The expectation is that the Associate Scientist will have experience independently executing mRNA process development experiments and production efforts. Reporting to Scientist, Process Development, the right candidate will be a strategic thinker that brings a leadership presence and enthusiasm for Strand along with a desire to conquer new challenges. | 8/30/2022 |
| 6171 | Strand Therapeutics Boston, MA Research Technician B.S. Exp: 0.5-1 years |
We are looking for a highly motivated and innovative candidate for the role of Research Technician. Reporting to the Sr Scientist of Vector Engineering, this individual will provide support to various R&D teams to help streamline daily research operations. The ideal candidate will have experience with mammalian cell culture, media preparation, cell line maintenance and reagent/inventory management of lab essentials. The candidate will be expected to work in an innovative, fast-paced, cross-collaborative biotech environment and contribute to multi-disciplinary team activities to advance our platform. | 8/30/2022 |
| 6172 | Sutro Biopharma San Carlos, CA Associate Engineer / Engineer, MSAT (San Carlos, CA) BS or MS in Chemical/Biochemical Engineering, or Biological Sciences, or relevant field. Exp: Associate Engineer: 0 – 3 years |
Sutro Biopharma, Inc. is looking for an energetic and talented professional to join its MSAT Group. MSAT Group responsible for technology transfers, manufacturing support (investigations, change controls, CAPAs, process capability/monitoring/capacity/efficiency/quality improvements) and process validation. We are dedicated to making a difference in the lives of patients, both as individuals and as part of a team. The position will be based in Sutro’s, San Carlos, CA Manufacturing site. | 8/30/2022 |
| 6173 | Sword Diagnostics Chicago, IL Research Associate I BS or BA in biology, biochemistry or related field Exp: one to three (1 - 3) years |
Job Responsibilities: • Plan experiments with guidance from supervisor • Perform complex and critical laboratory experiments (primarily ELISA) with accuracy and precision • Analyze experiment results and recommend potential follow-on experiments • Follow all established company processes and procedures • Prepare buffers and other chemical solutions as needed • Other duties and responsibilities as assigned | 8/30/2022 |
| 6174 | TechLab Blacksburg, VA Research Technician B.A. or B.S. in a life science Exp: 1 year |
Job Summary The job of the Research Technician is to aid the Research Associate, Research Scientists, and Senior Research Scientists with experiments and research. The Research Technician can be expected to perform protein purification using chromatography, write Standard Operating Procedures and Master Batch Records, and assist with assay development and optimization. The Research Technician will report to a Senior Research Scientist. | 8/30/2022 |
| 6175 | Tenaya Therapeutics South San Francisco, CA Molecular Biology RAII SRAI or SRAII Upstream Process Development BS/MS in a biological science Exp: RA II: 1-3 Years |
Seeking a Qualified Candidate for a RAII/SRAI/SRAII within the Process Development Team. You will design, assemble, propagate and characterize constructs to support development projects and pipeline operations. This role will also have the opportunity to lead development of novel constructs and characterization. An ideal candidate strives to complete project milestones within departmental/corporate timelines and strategically executes protocols to troubleshoot complex operations and assays as needed. | 8/30/2022 |
| 6176 | Tessera Therapeutics Somerville, MA Research Associate/Senior Research Associate , RNA Analytics - HPLC BS. / M.S. or equivalent in a relevant discipline Exp: 1 - 2 years |
Tessera is seeking a Research Associate (RA) to join the analytical team to characterize synthetic oligonucleotides and mRNA using HPLC. The position will require creativity, resourcefulness, and adaptability. We are searching for experienced, enthusiastic, innovative, and highly motivated individuals who are comfortable working in a fast-paced entrepreneurial environment. | 8/30/2022 |
| 6177 | Tessera Therapeutics Somerville, MA Research Associate/Senior Research Associate, Cell Therapy Discovery BS/MS degree in biological sciences Exp: 1+ years |
We are looking for a Research Associate to join the Cell Therapy Discovery team to advance early-stage cell-based research with Tessera’s novel Gene Writing and Gene Rewriting technology for ex vivo and in vivo cell therapy applications. The Senior Research Associate will work closely with scientists in the Cell Therapy team to translate novel gene writing technologies to develop innovative therapeutics for Oncology disorders. We are searching for a driven, enthusiastic and self-motivated individual who is comfortable multitasking and working independently on various aspects of the platform. This individual will join a dynamic, rapidly growing, and highly collaborative team. | 8/30/2022 |
| 6178 | Tessera Therapeutics Somerville, MA Research Associate I/II, High-throughput mRNA Manufacturing (Contract) BS/MS degree in either Chemical Engineering, Bioengineering, or Biological Sciences. Exp: 1+ years |
Tessera Therapeutics is seeking a motivated and creative Research Associate I (or Research Associate II) to join a team of scientists and engineers focused on process development of mRNA. This is a contract position through the end of the year. This will include, but not limited to, high-throughput production process development and automation, mRNA manufacturing, process execution to make material for preclinical studies. This individual will join a dynamic, rapidly growing, and highly collaborative team that is driving RNA process development for a novel platform of Gene Writing. | 8/30/2022 |
| 6179 | Tri-Pac South Bend, IN Assistant Engineer Bachelor's Degree in Engineering or Science discipline Exp: 0-2 years |
The Assistant Engineer will demonstrate his/her knowledge of biologics manufacturing processes, including fermentation, purification, and bulk filling processes and work independently in a team environment, influencing team decisions, and exercising sound judgement in determining compliant and robust validation approaches. He/she will have the ability to multi-task with a demonstrated track record in meeting deliverable timelines and must demonstrate the ability to think critically and analytically with acumen for troubleshooting and problem solving and is a strong team player aligned with company corporate values. This individual will have good interpersonal, verbal, and written communication skills and can function effectively and independently in a fast-paced and dynamic environment. He/she is self-motivated and willing to tackle assignments and development opportunities outside of job scope as needed. Demonstrates hands on experience with facility/equipment/utility qualification, cleaning validation, process validation, and sterilization validation experience in GMP environment and with CIP/SIP cycle development. | 8/30/2022 |
| 6180 | Tri-Pac South Bend, IN Laboratory Technician Associates or Bachelor’s degree in a scientific field preferred Exp: 1-2 years’ |
The Lab Technician performs chemical analysis and testing on chemical raw materials and in-process/finished batches according to methods and specifications as defined by the customer. He/she assists with compiling, analyzing and interpretation of results as well as maintaining the flow of samples and paperwork through the laboratory. The Lab Technician maintains laboratory equipment and instrumentation to ensure ideal usage and has a strong attention to detail. The Lab Technician is able to effectively correspond with internal customers, has excellent organizational skills, able to perform physically demanding work such as moving and lifting equipment and capable of standing for long periods of time. | 8/30/2022 |
| 6181 | Tris-Pharma Monmouth Junction, NJ Associate QC Analytical Chemist Bachelors in Chemistry or related scientific field Exp: 0-3 years |
We have an immediate opening in our Monmouth Junction, NJ QC Lab for an (Associate) QC Analytical Chemist. This is an entry level scientific position and we will train qualified candidates who meet listed requirements. Recent college graduates are welcome to apply. The (Associate) Quality Control (QC) Analytical Chemist performs analytical testing of raw materials, packaging components, in-process (IP), finished product (FP), and/or stability samples (ST). She/he is also responsible for following Analytical Methods, current Good Manufacturing Practices (cGMPs), Protocols, Standard Operating Procedures (SOPs) and company policies. | 9/1/2022 |
| 6182 | Tris-Pharma Monmouth Junction, NJ AR&D Scientist - ALL LEVELS Bachelors degree in Chemistry or related scientific field Exp: 1 year |
To support expectations of continued growth Tris is expanding the Laboratories at our Monmouth Junction, NJ facility and has openings for all levels of Analytical Research and Development (AR&D) Scientists. | 9/1/2022 |
| 6183 | TScan Therapeutics Waltham, MA Research Associate/Sr. Research Associate, Translational Research (RA30-1) BS/MS Exp: BS: 0-5+ years; MS: 0-2+ years |
TScan Therapeutics is a clinical-stage biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for a highly motivated researcher to join our Translational team as Research Associate/Senior Research Associate, supporting both pre-clinical and clinical-stage programs. The ideal candidate should have relevant experience in primary T cell culture, immunoassays, flow cytometry, and cancer biology, and enjoy exciting, collaborative, and vibrant startup culture. A team player with a sense of urgency will thrive in this role. | 9/1/2022 |
| 6184 | TScan Therapeutics Waltham, MA Research Associate/Senior Research Associate, In Vivo Pharmacology (RA07-7) BS/MS Exp: For RA level: BS and 0-3+ years; For Sr. RA level: MS and 0-2+ years |
TScan Therapeutics is a startup biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for a motivated researcher to join our In Vivo Pharmacology team as a Research Associate/Senior Research Associate, supporting the preclinical development of our lead therapeutic TCRs. The ideal candidate should have relevant experience in in vivo pharmacology, mechanism of action and anti-tumor efficacy studies, and enjoy fast-paced, collaborative, and vibrant startup culture. A team player with a sense of urgency will thrive in this role. | 9/1/2022 |
| 6185 | TScan Therapeutics Waltham, MA Computational Research Associate/Senior Research Associate (RA02-8) Master’s degree Exp: 1+ years |
TScan Therapeutics is a startup biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for a motivated bioinformatician/computational biologist to join our team as Computational Research Associate, supporting our novel target identification and validation workflow in house, with focus on Next Generation Sequencing and genomic data analyses. The ideal candidate should have relevant experience in genomics, computer science and bioinformatics, and enjoy fast-paced, collaborative and vibrant startup culture. A team player with a sense of urgency will thrive in this role. | 9/1/2022 |
| 6186 | Twist Bioscience South San Francisco, CA Research Associate B.S. or M.S. in Molecular Biology, Biochemistry, Chemistry or a closely-related field Exp: 0-2 years |
This position is geared towards working with the DNA and RNA product lines. The candidate must be capable of maintaining current products, troubleshooting control fragment assembly issues, and analyzing data related to current and future controls. Up-and-coming scientists that demonstrate self-motivation and enthusiasm for scientific bench work are strongly encouraged. Your work will be mainly at the bench; however, you will have the opportunity to use high-throughput robotic instruments as well as coding and bioinformatics tools to expand your expertise. You will work alongside and learn from some of the best scientists and bioinformaticians in the business. | 9/1/2022 |
| 6187 | Twist Bioscience South San Francisco, CA Research Associate, Antibody Engineering BS Exp: 1-year |
We are seeking an outstanding, innovative, and creative Research associate to join our antibody discovery effort. This research associate will play multiple roles within the Biopharma group and will work within a team responsible for antibody discovery utilizing a number of in vitro display technologies, e.g. phage display, ribosome display, and yeast display. | 9/1/2022 |
| 6188 | Twist Bioscience South San Francisco, CA Research Associate, NGS Bachelors/ Associates degree in biology, chemistry, biochemistry Exp: 1-3 years |
Twist is seeking a highly motivated individual to help support customers and their Next Generation Sequencing needs. This individual will work closely with R&D and Customer Support teams to help develop custom solutions for various sequencing applications. The candidate will be detail oriented who is compatible with fast paced environments. | 9/1/2022 |
| 6189 | Twist Bioscience South San Francisco, CA Research Associate, NGS Viral Controls B.S. or M.S. in Molecular Biology, Biochemistry, Chemistry or a closely-related field Exp: 0-2 years |
This position is geared towards working with the DNA and RNA controls product lines. The candidate must be capable of maintaining current products, troubleshooting control fragment assembly issues, and analyzing data related to current and future controls. Up-and-coming scientists that demonstrate self-motivation and enthusiasm for scientific bench work are strongly encouraged. Your work will be mainly at the bench; however, you will have the opportunity to use high-throughput robotic instruments as well as coding and bioinformatics tools to expand your expertise. You will work alongside and learn from some of the best scientists and bioinformaticians in the business. | 9/1/2022 |
| 6190 | Twist Bioscience South San Francisco, CA Research Associate, Process Development B.S. Molecular Biology, Biochemistry, Chemistry, or a closely-related field. Exp: 1-4 years |
We are looking for an outstanding Research Associate to join our Specialty Production Team in South San Francisco. The Research Associate will support the production team’s custom DNA-based applications and assays for synthetic biology including high-throughput gene synthesis, high-throughput cloning processes, and NGS-based QC. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast-paced startup environment. The ideal candidate will work independently, be very organized, have excellent molecular biology knowledge and skills, and communicate effectively with peers/management. The Candidate must be comfortable working in a LEAN manufacturing/ controlled laboratory environment. | 9/1/2022 |
| 6191 | Twist Bioscience South San Francisco, CA Research Associate, Specialty Production B.S. Molecular Biology, Biochemistry, Chemistry, or a closely-related field. Exp: 1-4 years |
We are looking for an outstanding Research Associate to join our Specialty Production Team in South San Francisco. The Research Associate will support the production team’s custom DNA-based applications and assays for synthetic biology including high-throughput gene synthesis, high-throughput cloning processes, and NGS-based QC. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast-paced startup environment. The ideal candidate will work independently, be very organized, have excellent molecular biology knowledge and skills, and communicate effectively with peers/management. The Candidate must be comfortable working in a LEAN manufacturing/ controlled laboratory environment. | 9/1/2022 |
| 6192 | Ultragenyx Pharmaceutical Woburn, MA Research Associate, Analytical Development - Gene Therapy BS in Biology, Biological Science, Genetics or a related discipline Exp: 0-2 years |
Working in close collaboration with other Analytical Development team members, the Research Associate will perform analytical testing for AAV gene therapy vectors and be involved in method development and optimization. This researcher will be highly involved in analysis of AAV therapeutic materials with molecular and genomic analytical methods to support process development, product characterizations, and QC release testing. We are looking for an individual with proven ability to work collaboratively with other researchers to finish projects within timelines and to work creatively under supervision. | 9/1/2022 |
| 6193 | Ultragenyx Pharmaceutical Cambridge, MA Contract Research Associate I, Non-Clinical (Temporary) B.S. or equivalent degree in biology, molecular biology, biochemistry, virology or related discipline Exp: 1 year |
The candidate will support advancement of innovative AAV-based therapeutics by using a variety of research methods including mammalian histology, molecular and biochemical techniques, as well as cell-based assays | 9/1/2022 |
| 6194 | Ultragenyx Pharmaceutical Cambridge, MA Research Associate, Vector Core - Gene Therapy BSc in Biology, Molecular Biology, Biochemistry, Virology or cognate discipline Exp: 1-2 years |
Reporting to the Senior Director of Vector Platform Research, the Research Associate will support and execute the production and purification of rAAV from HEK and HeLa Producer Cell Line systems, as well as iterative improvement of these processes by performing hypothesis-driven research. Core Lab & Ops: This role typically requires that the majority of the work be conducted on-site and thus will be subject to certain on-site safety protocols during the pandemic. | 9/1/2022 |
| 6195 | Variantyx Framingham, MA NGS Laboratory Technician BSc, MSc in life sciences/Biology/Molecular Biology/Biochemistry or related field. Exp: 1 year |
The NGS Laboratory Technician performs high complexity laboratory testing on patient specimens across various assays and platforms. This role will be performing quality control and quality assurance procedures while complying with all applicable local, state and federal laboratory requirements. Including CAP/CLIA and NY State Requirements. The Laboratory Technician is an on-site position in Framingham, MA; Full time 2nd shift, 3rd shift or weekend shift. | 9/1/2022 |
| 6196 | Verve Therapeutics Cambridge, MA Research Associate/Sr. Research Associate, gRNA Technology M.S. or B.S. in biological sciences, chemistry, or biomedical/chemical engineering Exp: 0-4 years |
We are seeking a Research Associate to join a team focused on developing gRNA technology, including chemical modification, sequence design, and early-stage process development of gRNA for Verve’s novel CRISPR gene editing therapies. The ideal candidate will have interest in nucleic acid technology, biochemistry, and analytics, and a desire to apply creative problem-solving skills to develop RNA constructs and evaluate production processes. In this highly cross-functional role, you will perform a wide range of experiments to support projects across different functional areas throughout Verve R&D and Tech Ops. | 9/1/2022 |
| 6197 | Vesigen Therapeutics Cambridge, MA Research Associate I-II, Tissue Culture Core Master’s degree Exp: 1-3 years |
Vesigen is seeking a creative and highly motivated Research Associate to join our team and help advance the development of the company’s exciting ARMMs technology. The candidate will be an integral member of the R&D team, with opportunities to learn and contribute and develop numerous preclinical programs across several therapeutic areas. | 9/1/2022 |
| 6198 | Vir Biotechnology San Francisco, CA Research Associate II MA/MS Exp: 1 years |
Vir Biotechnology is seeking a motivated and collaborative Research Associate to help drive new efforts in the discovery and development of novel therapies for the treatment of infectious disease. You will work within a highly collaborative group environment with other passionate scientists. The successful candidate, under guidance, will participate in discovery and translational research efforts aimed at identifying and characterizing novel therapeutic targets, investigating mechanism of action of therapeutics and defining optimal drug combinations through evaluation in the appropriate in vitro models. | 9/1/2022 |
| 6199 | Voyager Therapeutics Cambridge, MA Research Associate II, In Vivo Biology B.S. or M.S. in Biology or related discipline Exp: 1 to 3 years |
We are seeking an experienced and highly motivated biologist to contribute to our biochemical and in vivo research team at our facility in Cambridge, Massachusetts. This is an ideal position for an individual with a background in vivo biology and biochemical methods, who thrives in a team-oriented, fast-paced, and cross-disciplinary small biotech environment. The individual will work at the bench on multiple projects and be responsible for experimental execution and data analysis for research studies supporting therapeutic programs and platform discovery research. We are looking for prior hands-on experience with protein purification, ELISA, western blot, mouse handling, perfusion and tissue collection. | 9/1/2022 |
| 6200 | Voyager Therapeutics Cambridge, MA Research Associate/Senior Research Associate, Assay Development Bachelor’s degree in Molecular/Cellular Biology, Biochemistry, Pharmacology or a similar field Exp: 1-5 years |
We are seeking an experienced and highly motivated Research Associate or Senior Research Associate to contribute to our Translational Research team at our facility in Cambridge, Massachusetts. This is an ideal position for an individual with a strong background in molecular and biochemical assays and methods development, who thrives in a team-oriented, fast-paced, and cross-disciplinary small biotech environment. The successful candidate will participate in the development, implementation, and execution of assays to assess vector biodistribution, transgene expression, and pharmacodynamic effects in ex vivo tissues from preclinical gene therapy program studies and novel capsid discovery platform studies. | 9/1/2022 |
| 6201 | Promega San Luis Obispo, CA Manufacturing Associate B.S./BSE degree Exp: 1-3 years |
This position is responsible for performing a variety of basic operations, under direct supervision, to manufacture bioluminescent and fluorescent chemical products which are used as tools to study gene functions, enzymes, drug interactions, metabolism and more. This is an interesting and challenging role on a highly energetic and talented team. This position is full-time, 40 hours per week. | 8/22/2022 |
| 6202 | Protomer Technologies Indianapolis, IN Associate Oligonucleotide Chemist BS and/or MS in Chemistry, Biochemistry, or related field Exp: 1-2+ years |
In the RNA Therapeutics Team, both basic and applied sciences are vital. We are looking for creative and energetic problem solvers to join a multidisciplinary team at the front edge of innovation. Key facets of the role are solid-phase synthesis of custom nucleic acid oligomers and conjugation of ligands for specific cellular and tissue delivery to progress an innovative preclinical portfolio. We are building state-of-the art expertise in major oligonucleotide-based modalities and delivery approaches, with an emphasis on innovative approaches with potential for breakthrough efficacy. You will join our fast-paced, interdisciplinary team as we utilize novel RNA/oligonucleotide based therapeutic modalities to enhance the Lilly portfolio. The successful applicant will utilize their knowledge and technical expertise to complement and enable core capabilities and help drive the revelation and development of RNA-based clinical candidates. Do you have an aptitude for innovative approaches and modalities in discovery and development focused on identifying impactful therapies for the patient? We want you on our team! | 8/23/2022 |
| 6203 | Protomer Technologies New York, NY Research Associate, Analytical Development BS and/or MS Exp: 1+ years |
The Analytical Development (AD) team is a group of energetic, brilliant, fun, and motivated individuals. We independently work on different AAV-based gene therapy programs while continuously working as a team to achieve our goals. We are a small but quickly growing family. This groupAD is responsible for developing robust and innovative analytical methods to support internal and external manufacturing processes. While much of the day-to-day operations required wet-lab work, our team focuses on not only building everyone’s technical expertise but also fostering an environment for career growth as scientists in the biopharmaceutical industry. The Research Associate will be responsible for the development and establishment of novel analytical methods for characterization of AAV-based products. | 8/23/2022 |
| 6204 | Protomer Technologies Indianapolis, IN Chemist - Oligonucleotide Synthesis BS and/or MS in Chemistry, Biochemistry, or related field Exp: 1-2+ years |
The Lilly Genetic Medicines Team is looking for collaborative creative and energetic problem solvers to join a multidisciplinary team at the front edge of innovation. You will join our fast-paced, interdisciplinary team as we utilize novel RNA/oligonucleotide based therapeutic modalities to enhance the Lilly portfolio. The successful applicant will utilize their knowledge and technical expertise to accelerate the core capabilities and development of internal RNAi-based clinical candidates. Do you have an aptitude for large scale oligonucleotide synthesis and have a desire to learn about RNAi modalities in discovery and development that focus on identifying impactful therapies for the patient? We want you on our team! | 8/23/2022 |
| 6205 | Protomer Technologies San Diego, CA Associate - Protein Mass Spectrometry Masters in chemistry, biochemistry or a similar field Exp: 0 years |
The Protein Biosciences group at the Lilly Biotechnology Center San Diego seeks a BS or MS level scientist with experience in protein mass spectrometry to join a team responsible for the expression, purification, and characterization of protein therapeutics. The primary focus of this position will be the characterization of proteins. | 8/24/2022 |
| 6206 | Protomer Technologies Branchburg Township, NJ Quality Control Lab Systems Analyst Bachelor’s Degree in a scientific field related to the lab (e.g., Chemistry, Microbiology or Biology) Exp: 1 year |
This position will provide in depth support to the QC laboratories for new and existing computerized laboratory systems and databases. Assist in the selection, implementation, maintenance, and continuous improvement of computerized systems within the QC laboratories. Serve as a technical lead on system implementation and validation projects and serve as a technical representative on project teams. Provides technical support in the diagnosis and resolution of QC computerized system issues. Identify compliance and data integrity issues related to QC computerized systems and implement effective resolutions. | 8/24/2022 |
| 6207 | PTC Therapeutics South Plainfield, NJ BS/MS Biologist ( Nucleotide Repeat Disorders) BS/MS Biologist ( Nucleotide Repeat Disorders) BS/MS Biologist ( Nucleotide Repeat Disorders) Master’s degree in a scientific discipline, preferably Biology or Biochemistry or Neuroscience Exp: 0- 2 years |
The BS/MS Biologist is responsible for performing scientific experiments that contribute to research and drug discovery activities at PTC. This position assists in the conduct of early-stage research, the goal of which is the identification of New Chemical Entities (NCEs), as well as the advancement of research programs from the identification of screening hits to advanced lead optimization. The incumbent is also responsible for communicating experimental results to his/her supervisor and the project team. | 8/24/2022 |
| 6208 | Purdue Pharma Wilson, NC Chemist BA or BS degree in Chemistry or closely related science. Exp: six months - two years |
The Quality Specialist I, Chemist is responsible for supporting the operations and manufacturing process by performing routine and non-routine analytical testing and GMP review in support of the analysis of raw materials, packaging components, ancillary solutions, in-process samples, finished product method development and/or transfers, cleaning/process validations, and stability samples. Will follow standard procedures in accordance with cGMP, GLP, DEA and company policies and procedures. | 8/24/2022 |
| 6209 | Purigen Biosystems Pleasanton, CA Research Associate - I/II B.S. in Molecular Biology, Biology, Biochemistry or similar life sciences discipline Exp: 1-3 years |
Purigen Biosystems, Inc., a Venture-backed, life science tools start-up company in the San Francisco bay area, is seeking an experienced Research Associate to join our Operations team. The Research Associate will be responsible for growing and maintaining various cell lines for quality control and product validation testing and performing a variety of tests on our unique Sample Preparation Instrument. This is a hands-on position for the highly qualified, self-motivated candidate who wants to enable cutting-edge life sciences technologies in a fast-paced, start-up environment. | 8/24/2022 |
| 6210 | Qiagen Germantown, MD Associate Scientist, Assay Development MS degree Exp: 1+ years |
Contribute to a team working on the design, development and improvement of immunodiagnostic assays based on ELISA and/or lateral flow technology. Coordinating with other team members to enable the planning and execution of studies accurately and timely. Execute feasibility and verification studies as required. Recording and analyzing experimental data and results, verifying data integrity and accuracy, and reporting on findings to the team. Maintaining accurate laboratory notebooks in a timely fashion and provides input to technical reports covering data Propose novel strategies and technologies and independently apply basic scientific principles to solve problems. Perform literature searches and have a broad knowledge and deep understanding of literature in Immunoassay and infectious disease fields. Review method development data, verification/validation reports, and bioanalytical reports. Thoroughly analyze results and methods, solve analytical problems, and troubleshoot assays. | 8/24/2022 |
| 6211 | Qiagen Beverly, MA Lab Technician I Bachelor’s degree from four year college or university Exp: 0-2 years |
The Lab Technician I performs assigned manufacturing support duties in a ISO 13485 environment. Job performance will involve a variety of activities including: - Ensure the cleanliness and availability of glassware and labware for production use. - Operate autoclave and ensure sterility of equipment and associated labware - Operate Lancer glasswasher and ensure the cleanliness of labware. - Ensure the Sanitization area is appropriately stocked. - Prepare buffers and solutions. - Communicate as a team member with other functional groups, via face to face, email and written reports. | 8/24/2022 |
| 6212 | Qiagen Beverly, MA Protein Purification Technician I Bachelor’s degree from four year college or university Exp: 1-2 years |
The Protein Purification Technician I performs assigned manufacturing and process development duties in a ISO 13485 environment. Job performance will involve a variety of activities including: - Execute development and production scale purification protocols as directed. - Work with standard scientific equipment as described in relevant procedures; AKTA Purifier and AKTA Pilot, UV spectrophotometer, balances, chromatography columns, SDS-PAGE, autoclaves, pH meter, refrigerators, freezers, biohazard safety cabinets. - Record results in laboratory notebooks; required to have meticulous organization and record keeping skills. - Prepare buffers and solutions. - Communicate as a team member with other functional groups, via face to face, email and written reports. Position Requirements | 8/24/2022 |
| 6213 | Qiagen Beverly, MA Protein Purification Technician II Bachelor’s degree from a four year college or university Exp: 1 – 3 years |
Responsibilities of the Protein Purification Technician II will primarily include activities directly related to the purification of proteins (enzymes and antibodies). Execute development and production scale protein purification procsses as specified. Perform standard operations as described in relevant procedures. This includes the following: Column chromatography via AKTA Purifier and Pilot system Upstream process separation techniques such as homogenization, cell lysis, and centrifugation Sample analysis via chromatogram, UV Spectroscopy and SDS PAGE Packing and evaluation of a variety of different columns Buffer and solution preparation Small scale bacterial fermentations Perform all activities in an ISO 13485 environment | 8/24/2022 |
| 6214 | Quidel San Diego, CA Development Associate II (Assay Development) MA/MS in life sciences Exp: 0-2 years’ |
Responsibilities include activities to support research and new product development. Perform self-directed experiments or as directed by Scientist or Manager · Resolve product performance issues · Summarize experimental data, draw conclusions and make recommendations · Conduct research, process development, validations, creation and implementation of documentation and training of personnel · Maintain project documentation and laboratory notebooks in accordance with internal Quidel and external regulatory requirements as part of the design control process · Maintain a safe working environment | 8/24/2022 |
| 6215 | QuVA Pharma Bloomsbury, NJ Chemist B.S. or M.S. degree in chemistry, biology or related field Exp: 0- 2 years |
The individual will be required to perform either validation studies for analytical methods, conduct stability analyses on drug product, or test of Raw Materials. This individual will execute testing per current test methods and follow all applicable SOPs and cGMP guidelines. This individual will conduct analytical testing of finished sterile products, and raw materials, following all written procedures and cGMP, and providing documentation of analyses. This individual will report any issues to the Supervisor upon discovery. This individual will work with the Supervisor to understand overall expectations and execute them independently based on the prioritization of projects. This individual will work with the Supervisor or Manager to understand overall expectations and provide data to meet project milestones. | 8/24/2022 |
| 6216 | QuVA Pharma Bloomsbury, NJ Microbiologist B.S. degree in related field (preferably Microbiology) Exp: 0-2 years |
Performs individual hands-on work in the sterility testing program. The Microbiologist provides scientific guidance and interpretation of environmental monitoring and microbiology results to production management. | 8/24/2022 |
| 6217 | Reaction Biology Malvern, PA QC Specialist – Biochemical Assays Master’s degree in a related field Exp: 1+ years |
We are currently seeking a QC Specialist for our Malvern, PA facility. We are looking for a reliable and motivated individual with a strong science background to work in our lab. The successful candidate will provide quality control review of laboratory records, reports, and other documentation for accuracy, appropriateness, and timeliness. | 8/24/2022 |
| 6218 | Reaction Biology Malvern, PA Research Associate I – Biochemical Assays Research Associate I – Biochemical Assays Bachelor’s Degree or equivalent in biochemistry or related discipline Exp: 0-3 years |
We are currently seeking a Research Associate I for our Malvern, PA facility. We are looking for a reliable and motivated individual with a strong science background to work in our lab. The position is a bench position with the primary duty of executing a variety of enzymatic assays. | 8/24/2022 |
| 6219 | Resursion Pharmaceuticals Salt Lake City, UT Research Associate, In Vitro Pharmacology Masters degree in cell biology or related field Exp: 1+ years |
You’ll join a team focused on developing and screening in vitro assays for the world’s leading company in AI-guided drug discovery. You will help develop the technology and build the assays used to discover potential therapeutics and determine how and where they interact with human biology. With treatments for hundreds of diseases in our sights, you will work on a diverse array of programs side-by-side with automation engineers, biologists, chemists, data scientists, software engineers, and many others. Together, we generate the data, systems, tools, and methods to accelerate the discovery of treatments for pathologies that affect the lives of countless individuals. | 8/24/2022 |
| 6220 | Minaris Regenerative Medicine Mountain View, CA QC Analytical Associate I BA/BS in a science or relevant field required Exp: 0-2 years |
The Quality Control Analytical Associate serves as a support role to clinical and commercial production. The QC Analytical Associate will assist with process check point, stability, and release analytical testing to ensure that quality standards are upheld for all products produced at the facility. | 8/24/2022 |
| 6221 | Minaris Regenerative Medicine Allendale, NJ QA Associate II BS or higher education degree in a scientifically related field Exp: 1 -3 years |
The Quality Assurance Associate II is responsible for performing Quality Assurance activities under direct supervision of daily tasks in support of Quality Systems and/or client procedures including but not limited to document management, review of QC data, material releases and final product releases as well as assisting Quality management with department needs. | 8/24/2022 |
| 6222 | SAMDI Tech Chicago, IL Research Assistant B.S. in biology, biochemistry, chemistry, or related field Exp: 0-3 years |
The Research Assistant will be an active member of our dynamic Research Team. The Research Team leads target/enzyme-based projects for biotech and pharma clients to develop biochemical assays for high-throughput screening and characterization of drug candidates and reaction mechanisms. | 8/25/2022 |
| 6223 | Sanofi Pasteur Chattanooga, TN Quality Control Lab Chemist I Bachelor’s degree in Chemistry or related field. Exp: Zero to three years |
Role Responsibilities Perform testing of ingredients as required to support production requirements. Assure that testing is properly documented and that the ingredient is dispositioned in accordance with the results of the test and the appropriate standard operating procedures. Perform routine laboratory testing for bulk and finished product to support production or shipping requirements. Assure that testing is properly documented and that the bulk or finished product is dispositioned in accordance with the results of the test and the appropriate standard operating procedures. Perform stability testing in support of the room temperature stability program. Assure that stability testing is completed in a timely manner and within the designated time frame. Complete stability testing documentation as appropriate. Knowledge of and ability to use lab instruments including but not limited to: UV-VIS, HPLC, GC, ICP, AA, and FTIR. Secure and file the MSDS sheet for all laboratory chemicals and reagents. Maintain a log of laboratory chemicals and reagents. Assure that chemicals and reagents are within their respective expiration date or shelf life. Discard any expired or obsolete chemicals or reagents as appropriate. Oversee the proper disposal of laboratory waste in conformance to the established procedure. | 8/25/2022 |
| 6224 | Sanofi Pasteur Swiftwater, PA Quality Control Technician - Vaccine Bachelor Degree or Mater Degree in Microbiology or Biological Sciences Exp: 0-5 years’ |
KEY RESPONSIBILITIES: This position supports execution of routine testing in the Quality Control Microbiology laboratory while strictly adhering to site work instructions, Federal Regulations, cGMP, and Sanofi Pasteur policies and procedures. This position requires the individual to perform route testing as scheduled to support production, method validation as well as the stability program and completing required documentation. Knowledge of general Microbiological techniques including aseptic processing and culturing of both bacterial and viral isolates. Demonstrated knowledge and proficiency of functions within the following systems is required: SAP, Trackwise, LIMS, MASTER and eDoc. Activities include: Assist with maintaining safety and compliance of the laboratory work area; Perform cleaning of laboratories, equipment, and ancillary areas as required; Attend/Contribute to scheduled team meetings, department and safety meetings. This position requires proficiency and understanding of the theory related to processes, assays, and equipment as well as the ability to identify issues/trends. Participates in training activities including their individual professional development, creation/revision of training modules as well as provide training to others on processes, procedures, assays, and equipment with which they are proficient. Demonstrate proficiency in use and knowledge of change controls, CAPAs, and the QA deviation system. Perform initial deviation investigations through analyst interview. Develop a working knowledge of appropriate compendia and/or regulatory guidance. This position will be filled as off-shift which includes second shift or weekends. | 8/25/2022 |
| 6225 | Sanofi Pasteur Ridgefield, NJ Validation Specialist I Bachelor's degree in Engineering or Science discipline Exp: 1 years |
Summary of Responsibilities: Perform a variety of moderately complex to complex tasks with minimal supervision in accordance with current cGMP, company, and departmental standards in a given protocol. This may include calibrating test instrument, qualifying equipment, and validating simple processes. Perform hands on qualification / validation execution work, e.g. Autoclave sterilization, Steam-In-Place, Clean Validation, VHP Decontamination, Temperature Mapping and Environmental Smoke studies. Generate qualification / validation protocols and reports, from a set template, for repetitive systems or assist in protocol development of new equipment or system. This position is needed to work with minimal supervision or independently with direction, and the work will be reviewed for soundness of judgment and overall adequacy / accuracy. This position will also consistently require to make independent decision and to exercise independent judgment. In addition, the duties of this position require advanced knowledge in specialized field of learning, e.g. Moist Heat Sterilization, Isolator with VHP Decontamination, Stability Chamber / Temperature Control Unit, simple equipment and Laboratory Instrument, simple PLC control system…etc. This position will also contribute to the completion of milestones associated with specific projects or routine technical tasks. Failures to achieve results or erroneous decisions or recommendation may cause delay in program schedule and may results in the allocation of additional resources. The position will be the primarily internal company contacts or infrequent inter organizational / outside customer contacts. | 8/25/2022 |
| 6226 | Sanofi Pasteur Framingham, MA Quality Control Analyst I Bachelor’s Degree Exp: 0-2 Years |
Shift Schedule: Sunday-Wednesday shift, 12:00 pm - 10:30 pm Quality Control Microbiology (QCM) is responsible for testing intermediate production samples, final product samples, and environmental samples to demonstrate that all products meet the standard requirements for CGMP operations. Additional functions include raw material testing, stability testing, assay transfers, and qualification of instrumentation. Quality Control is also responsible for assisting in site wide studies and projects. | 8/25/2022 |
| 6227 | Sanofi Genzyme Lexington, MA mRNA, Research Associate, Pre-Clinical Plasmid Production M.S. in a related field (e.g., Chemical Engineering, Biochemical Engineering, Biochemistry, Biotechnology) Exp: 1-3 years |
As an experienced molecular biologist, you will be supporting the design, development and implementation of a robust plasmid growth, extraction, and purification process for preclinical supercoiled and linearized plasmid production. | 8/25/2022 |
| 6228 | Sanofi Genzyme Waltham, MA Research Associate, Genomic Medicine Unit CMC Cell Culture Process Development Bachelor’s degree in biological science or engineering discipline Exp: 0-1 years |
The cell culture process development group is responsible for viral vector production optimization and development of next generation production platforms to support high dose therapeutic products. The group is seeking a motivated Research Associate to join the team. | 8/25/2022 |
| 6229 | Sanofi Genzyme Framingham, MA Upstream Manufacturing Associate Upstream Manufacturing Associate Bachelor’s degree Exp: 1-3 years |
The Upstream Manufacturing Department performs small and large-scale cell culture operations, harvest filtration, and initial capture chromatography steps in a new manufacturing facility. The 24/7 large-scale therapeutic protein manufacturing facility uses single-use technology. The Upstream Department is responsible for all setup, operation, and breakdown of equipment associated with cell culture and capture column operations. This position is responsible for performing a variety of complex tasks under the general guidance and in accordance with the manufacturing instruction set and current GMPs. | 8/25/2022 |
| 6230 | Sarepta Therapeutics Columbus, OH Research Associate I/II, Gene Therapy R&D Research Associate I/II, Gene Therapy R&D B.A. or B.S. degree in biological sciences or related field Exp: 1-3 years |
Sarepta Therapeutics is seeking a motivated individual to provide laboratory support, perform experiments, collect and analyze data on in vitro and in vivo studies to investigate gene therapies for rare genetic diseases. Activities will include assessment of protein expression, tissue pathology, and disease phenotype in animal models of neuromuscular disorders. The RA participates in development, GCP/GLP qualification, and validation of biomarker assays to support preclinical development, clinical trials and clinical development decision-making. | 8/25/2022 |
| 6231 | Sarepta Therapeutics Andover, MA Associate I ELISA Associate I ELISA Bachelor’s degree in molecular or cell biology Exp: 0 - 2 years |
This individual will join a dynamic and vibrant team to support quality control laboratory activities for the development of AAV therapeutics conducted at Sarepta Andover facility. The individual will assist in conducting ELISA assays to support QC release and method validation. The individual may work under the direction of a subject matter expert conducting experiments and support analytical method validation and qualification activities. All aspects of this position involve working in a GMP compliant manner. | 8/25/2022 |
| 6232 | Sarepta Therapeutics Andover, MA Associate II - rcAAV B.S. or M.S. degree in molecular biology or cell biology Exp: QC Associate I/II: 0 – 2 years |
This individual will support quality control activities conducted at Sarepta Andover facility in the field of AAV therapeutic release and stability. The individual will perform Replication Competent Adeno-associated virus (rcAAV) Detection assay using Quantitative Polymerase Chain Reaction, qPCR as endpoint readout of release and stability samples for early/late phase clinical and commercial AAV therapeutic products. This individual may assist in troubleshooting rcAAV assays being conducted in Andover, MA and at contract testing laboratories. All aspects of this position involve working in a GMP compliant manner. The individual will lead a team engaged in conducting rcAAV assays in support of release and stability of commercial AAV therapeutic products. This individual will also be responsible for supervising and training 1-3 junior QC associates as well management of their performance. | 8/25/2022 |
| 6233 | Sarepta Therapeutics Andover, MA Gene Therapy Potency Associate B.S. degree in molecular biology or cell biology Exp: QC Associate I/II: 0 – 2 years |
This individual will support quality control laboratory activities conducted at Sarepta Andover facility in the field of AAV therapeutic release and stability. The individual will assist in conducting GMP QC release and stability testing using state of art In vitro Potency Assay. The candidate should have hands on experience of SDS-PAGE, Western blotting, enzyme activity measurements, protein extraction and quantification methods. The position requires a background in cell culture, tissue lysate sample preparation, protein analysis and performing assays in a BSL-2 environment. The individual will work under the direction of a subject matter expert conducting experiments and support analytical method validation and qualification activities. All aspects of this position involve working in a GMP compliant manner. | 8/25/2022 |
| 6234 | ScienCell Research Laboratories Carlsbad, CA Associate Molecular Biologist Bachelor’s or Master’s degree in life science Exp: one-year |
We are searching for an energetic and self-motivated candidate with a positive attitude and strong work ethic to fill our associate molecular biologist position in our R&D department. Responsibilities include, but are not limited to, working on cell-derived DNA, RNA, and proteins purification, gene expression analysis, performing PCR/RT-PCT/qPCR, SDS PAGE and UV spectrum for quantitation. Candidates should be familiar with electrophoresis, spectrophotometer, centrifugation and other basic laboratory techniques. General lab logistical skills such as record keeping, ordering supplies and ensuring general laboratory safety and cleanliness are also required. | 8/25/2022 |
| 6235 | SDIX Newark, DE Biotechnician I BS/BA degree in biology, chemistry, or related field such as veterinarian studies Exp: 0 to 3 years |
Maintain laboratory in proper working order through organization and procurement of supplies, routine maintenance of laboratory equipment, organization and maintenance of reagents, and general laboratory hygiene. Verify and ensure that proper processes and procedures are followed in accordance with SOPs. Support manufacturing aspects of SDIX’s products by executing protocols, utilizing basic knowledge of biology, chemistry, laboratory equipment and computer software. | 8/25/2022 |
| 6236 | SDIX Windham, ME Biotechnician I BA/BS in biology, chemistry or related field such as veterinary studies. Exp: Up to 3 years |
This position supports manufacturing of SDIX’s products by executing protocols using basic knowledge of biology, chemistry, laboratory equipment and computer software. The Biotechnician I is responsible for conducting operations using various laboratory techniques, organizing and procuring supplies, and maintaining a clean and safe work environment. | 8/26/2022 |
| 6237 | Septodont Cambridge (Ontario Canada), CA Chemist I Bachelor's Degree in Chemistry or related discipline. Exp: One to two years |
The Chemist I is an entry-level position and is accountable to the Manager – Stability and Analytical Services. This person will be responsible for chemistry testing and review in the support of the Analytical testing and Tech Transfer for customer (CDMO) and R&D projects. | 8/26/2022 |
| 6238 | Sigmapharm Laboratories Bensalem, PA Associate Scientist AD BS in Chemistry or Pharmaceutical sciences Exp: 1-3 years |
Perform physical and chemical testing of raw material, packaging material, in-process, release, and stability samples. Record experimental data, analyze results, and maintain accurate and up-to-date notebooks. Support ANDA/NDA projects form development to approval with guidance. Support method development and method validation work. Assist in maintaining the laboratory in compliance with SOPs, CGMPs, FDA and OSHA. Use and maintain instruments, such as HPLC, GC, Dissolution, UV-VIS, IR, Titrator, etc. Troubleshoot and perform minor maintenance and repair of lab instrumentation. Support investigation and troubleshooting of analytical issues. | 8/26/2022 |
| 6239 | Smithers West Trenton, NJ Associate Research Scientist (Molecular and Cell Biology) MS in relevant field Exp: 1-2 years |
Smithers PDS LLC (Pharmaceutical Development Services) assists in the development of new medicines by providing bioanalytical services for all phases of drug development from discovery through approval and post market surveillance. PDS works with customers to develop new methods, validate existing methods, and perform the assays necessary to analyze samples from patients on more than 100 clinical trials. PDS is seeking an Associate Research Scientist with experience in Molecular and Cell Biology to join our team. The successful candidate is able to apply prior experience and knowledge to successfully perform in a laboratory environment under regulated conditions. | 8/26/2022 |
| 6240 | Smithers Wareham, MA Associate Chemist I - Environmental Fate and Metabolism B.S. degree in chemistry or related field Exp: 6 months |
Position is expected to perform a variety of routine tasks and often complex and difficult procedures independently and under supervision, in support of the conduct of normal laboratory operations. Individual is expected to detect and report problems in standardized procedures due to instrumental, sample, or test system failures. Performs a variety of routine, laboratory-based procedures. Responsible for understanding and routinely performing applicable Standard Operating Procedures, study specific protocol procedures and other laboratory assignments. This often includes recording instrument and apparatus readings on standard forms, preparation of test systems and recording and compiling laboratory data in real time in a complete and thorough manner for individual assignments. Responsible for maintaining cleanliness of the labs, storage and chamber areas as well as executing regular maintenance/calibration of equipment used on a regular basis. Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations as well as company policies. Duties are performed with minimal supervision. | 8/26/2022 |
| 6241 | NuProbe Houston, TX Technician I/II BA/BS or higher in Biology, Bioinformatics, or a related field Exp: 0 – 3 years |
The Technician I/II executes Research & Development activities which is vital to the success of the company. This position utilizes wet lab skills for executing qPCR and NGS experiments. Experience with analyzing NGS data using terminal/open-source tools and/or writing scripts in at least one language (python, R, Perl, Matlab etc.) is preferred. | 8/15/2022 |
| 6242 | NuProbe Houston, TX Technician I (Innovation) BA/BS or higher in Biology, Biochemistry, Biotechnology, or a related field Exp: 0 – 3 years |
The Research Technician I – Innovation Department executes most of the research & development protocol activity which is vital to the success of the company. This position handles sensitive data and comes with a high degree of trust. | 8/15/2022 |
| 6243 | NuVasive San Diego, CA Test Engineer, Verification Advanced degree in Biomedical, Electrical or Mechanical Engineering, or related technical discipline Advanced degree in Biomedical, Electrical or Mech Exp: 0+ years |
NuVasive is seeking an Electrical, Mechanical, or Biomedical Engineer with test development experience for our Surgical Intelligence System Test Engineering Team. Our team is part of a larger development group that focuses on integrating technology into products and systems designed for spine surgical use in the operating room. As our Human Factors Engineer, you will be working with a team to produce medical devices that are safe and effective for use by integrating the user experience into the design and development process. Your responsibility is to advocate for intended users and patient safety by minimizing potential use errors. In addition, you will participate in Design Validation and Usability studies by contributing to test plan development, developing test protocols, and helping prepare technical documentation for test reports. This is a hands-on role; outside of planning and documentation generation, you will be supporting formative and summative usability testing with end users and cadaver validation labs – a confident, passionate, and easy-going personality is a must for this role to work with multiple cross-functional teams and to interface with end-users (i.e., surgeons). | 8/15/2022 |
| 6244 | Ocean Ridge Biosciences Exton, PA Associate Quality Control Specialist-Biomarker Bachelor Degree or Master Degree in Chemistry, Biochemistry or other scientific field Exp: 0-2 years |
Review of Biomarker bioanalytical data (notebook documentation, raw data, and LIMS data) for accuracy, consistency, and completeness to ensure compliance with SOPs and GLP. Review method development/qualification/validation reports and sample analysis reports including text and data for accuracy and consistency. Preparation of bioanalytical test result data tables for clinical testing reports. Review of client data transfer specifications. Prepare and transmit client data transfer tables. Review Data Transfer Specification Other duties as assigned.Review of Biomarker bioanalytical data (notebook documentation, raw data, and LIMS data) for accuracy, consistency, and completeness to ensure compliance with SOPs and GLP. | 8/15/2022 |
| 6245 | Ocean Ridge Biosciences Hayward, CA Research Assistant-ADME BS in biology, biochemistry and other related fields Exp: 0-3 years |
We are looking for a highly-motivated Research Assistant to develop and conduct biochemical and cellular assays to evaluate potential therapeutics. Experience in cell line development, ELISA, PBMC biomarker, cell culture, cellular assays, gene expression is desirable. Prior experience in ADME assays including metabolite stability, drug transporter, CYP450, PPB and measurements of physicochemical properties is preferred. The candidate needs to be proficient in assay design, trouble-shooting, data analysis and working with 96-w & 384-w plate-based assays. The candidate needs to have a good understanding of drug discovery processes and experience in a discovery project is preferred. This position requires working with an interdisciplinary team of DMPK scientists, analytical chemists and pharmacologists. | 8/15/2022 |
| 6246 | Ocean Ridge Biosciences Hayward, CA Research Associate M.S. degree in related scientific discipline Exp: 0-3 years |
1) Perform Watson design according to Study Protocols 2) Conduct basic method development and validation studies. 3) Ability to troubleshoot and solve basic technical and instrumental issues. 4) Conducts and documents work in a regulated environment. 5) Reviews the data package and notebooks for junior chemists 6)Writing up analytical methods, protocols, and reports under supervision 7) Perform project communication with client, study director, and project management team under supervision | 8/15/2022 |
| 6247 | Ocean Ridge Biosciences Chicago, IL Analytical Chemist B.S. degree in chemistry Exp: 0-3 years |
Duties include methods transfer/development and validation, determination of analytes in dose formulations and accurate preparation of formulations (e.g., solutions, suspensions, etc.) to be used in toxicology studies. Knowledge of performing these duties with strict adherence to Good Laboratory Practice Regulations (FDA, EPA and OECD) is a plus. Other responsibilities as assigned. | 8/15/2022 |
| 6248 | Ocean Ridge Biosciences Hayward, CA Research Associate-Bioanalytical M.S. degree in related scientific discipline or B.S degree Exp: 1-3 years |
1)Execute established protocols and methods to assay small molecule compounds, their metabolites, and impurities in various chemical and biological samples. 2)Perform data analysis on LC/MS and HPLC instruments, with the ability to identify and troubleshoot inconsistencies as needed. 3) Perform analytical, pharmacokinetic/pharmacodynamic, metabolism data analysis. 4) Conduct basic method development and validation studies. 5) Conduct trouble-shooting and instrument maintenance of LC/MS. 6) Present and discuss data internally and externally. 7) Write reports under supervision. | 8/15/2022 |
| 6249 | Ocean Ridge Biosciences Hayward, CA Research Associate-Biologics MS / MA in biochemistry, biology, chemistry, pharmaceutics or related scientific discipline Exp: 0-2 years |
Conduct study design, lab-testing, data analysis and PI review. Author and/or review methods, protocols and other related documents. Assist PIs in maintaining project quality, meeting compliance requirements and timelines. Prepare notebooks, study binders, data packets, data summaries, methods, and qualification/validation protocols under the supervision of lab management / PIs Monitor reagent and consumable inventories and timely submit the orders for the support of both project and non-project based programs After receiving sufficient training, perform as PI and manage the overall planning, execution, and quality of assigned MD/MV and sample analysis projects under the supervision of lab management Participate TC and communicate with sponsors to solve technical issues and update projects, provide weekly summary to the sponsors | 8/15/2022 |
| 6250 | Ocular Therapeutix Bedford, MA Process Development Engineer I Bachelor’s degree in Chemistry, Biology, Biomedical or Chemical Engineering or related discipline. Exp: 0-2 years |
We are seeking an experienced engineer/scientist to execute drug product/process development project activities for hydrogel-based candidates. The role includes but is not limited to product design and evaluation, manufacturing process development, line layout and equipment procurement, and GMP manufacturing of clinical trial material. This individual will execute assigned project activities and work with project team members to develop and manufacture the drug products. They may oversee the execution of project tasks and monitor the activities and deliverables of project aspects in a leadership role. | 8/16/2022 |
| 6251 | Ology Bioservices East Norriton, PA Research Associate II, Process Development, Cell Therapy Bachelor’s or Master’s degree in immunology, cell biology, bioengineering or a related field. Exp: 1-3 years |
Resilience is seeking a talented Research Associate 2 to expand our cell therapy process development team. With the guidance of process development senior staff, this researcher will develop and optimize manufacturing processes for gene-modified cell products to advance Resilience’s biomanufacturing platforms and the clinical programs of Resilience’s partners. | 8/16/2022 |
| 6252 | Ology Bioservices Allston, MA Research Associate, Analytical Development Research Associate, Analytical Development Research Associate, Analytical Development Bachelor’s degree (B.S) or equivalent in Chemistry, Biochemistry or related field Exp: 0-2 years’ |
As a research associate in the nucleic acid franchise analytical development team the candidate will be responsible for executing analytical techniques in support of method development, qualification and routine testing support on client based and internal platform programs · Collaborate, assist, and design in method development of new assays and execution of lab procedures in support of nucleic acid process characterization and release methods for drug substance and drug product. · Methodologies include: molecular/PCR-based methods, nucleic acid sequencing, immunodetection, and fingerprinting approaches, aqueous and reversed phase chromatography, liquid-solid separation methods, and capillary and other gel electrophoresis methodologies. | 8/16/2022 |
| 6253 | Ology Bioservices Waltham, MA Research Associate II, Process Development, Stem Cells and Regenerative Medicine Bachelor’s or Master’s degree in cell Biology, immunology or a related discipline Exp: 1+ years |
Resilience is seeking a talented Research Associate II to join us as a valued member of the Cyto Innovation Process Development team. This researcher will focus on hands-on execution of protocols involving induced pluripotent stem cells (iPSCs) for Resilience’s developing Regenerative Medicine Modality. The successful candidate will support the development of Resilience’s best-in-class hypoimmune iPSC generation platform and will collaborate broadly with colleagues in platform R&D, analytical development, and other teams across the Resilience biomanufacturing network. | 8/16/2022 |
| 6254 | OpGen Rockville, MD Laboratory Technician BS degree Exp: 1+ years’ |
The Laboratory Technician will perform, implement, and improve laboratory workflows for NGS based detection of antimicrobial resistance. The Laboratory Technician will be responsible for delivering high quality lab results to our global partners, clinicians and microbiologists to derive actionable insights. | 8/16/2022 |
| 6255 | OpGen Rockville, MD Junior Scientist BS degree Exp: 1+ years’ |
The Junior Scientist will perform, implement, and improve laboratory workflows for NGS based detection of antimicrobial resistance. The Junior Scientist will be responsible for delivering high quality lab results to our global partners, clinicians and microbiologists to derive actionable insights. | 8/16/2022 |
| 6256 | OraSure New Brighton, MN Lab Technician I B.Sc. or M.S. degree in Biology, Biochemistry, Molecular Biology Exp: 1+ year |
Lab Technician I will be expected to work collaboratively as part of a team. In this role, the Lab Technician I will be responsible for managing timelines, performing hands-on lab work, maintaining processing records and working in compliance with our accreditations and quality standards. | 8/16/2022 |
| 6257 | Orna Therapeutics Cambridge, MA Research Associate/Senior Research Associate – RNA Production B.S. in biology, biochemistry or a related discipline required. Exp: one year |
We are seeking an exceptional researcher to join our team as a Research Associate/Sr. Research Associate to help build and maintain our proprietary RNA production process. The ideal candidate has at least a bachelor’s degree in a biological/biochemical related field with RNA handling and process development experience. They will be able to quickly learn, troubleshoot, and integrate new protocols into existing workflows; possess strong oral and written communication capabilities; demonstrate excellent collaboration & interpersonal skills; and be adept at problem solving in a fast-paced environment. | 8/16/2022 |
| 6258 | Pacira Biosciences San Diego, CA Microbiologist 1 BS degree in Microbiology or other life science Exp: 0 years |
The purpose of the position is to provide technical expertise in the area of pharmaceutical microbiology. The position functions in a cooperative effort to provide quality control and assurance to the operational departments involved in the manufacture of pharmaceutical products | 8/16/2022 |
| 6259 | Pall West Sacramento, CA Manufacturing Scientist -1 Bachelor’s degree or higher in a Science field Exp: 0-2 years’ |
The Manufacturing Scientist -1 for Beckman Coulter Diagnostics is responsible for the success and routine operations of a custom product, by supporting various elements of routine manufacturing, QC testing, equipment maintenance, troubleshooting, and inventory management of the product line. This position is part of the Technical Operations team located in West Sacramento, CA and will be on-site full-time. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. | 8/16/2022 |
| 6260 | Pall Cortland, NY Associate Scientist Bachelor’s degree Chemistry, Chemical Engineering, Materials Science Exp: 1-3 years |
The Associate Scientist or Engineer provides performance data to R&D, Marketing, Sales and Quality that enable their ability to serve our customers in the Microelectronics industry. They are part of a dynamic team that develops and standardizes new test methods that allows us to characterize our materials and products in ways that as closely as possible mimics their end-use. | 8/16/2022 |
| 6261 | Pall Madison, WI Associate Scientist I, Analytical Method Validation Bachelor’s degree in Microbiology, Biochemistry, Biotechnology, or related field Exp: 0-2 years |
The Associate Scientist I, Analytical Method Validation (AMV) in R&D is responsible for validating bioanalytical methods that are transferred either from clients or from the Analytical Method Development (AMD) group. This role will mostly focus on performing experiments to generate data to support validation of these methods. Duties include, but are not limited to, performing experiments, interpreting results, communicating results, and drafting documentation. The Associate Scientist I must interact closely with the AMD team to ensure that methods are transferred correctly. With guidance from the Senior Scientist, the Associate Scientist I executes validation protocols. The Associate Scientist I relies on education and experience to troubleshoot experiments, with technical oversight provided by the Senior Scientist, when necessary. The Associate Scientist I will also be qualified to train others on the methods they have validated. | 8/16/2022 |
| 6262 | Pall Westborough and Boston, MA Laboratory Operations Assistant Bachelor’s Degree Exp: one year |
The Accelerator Process Development group at Pall specializes in designing, optimizing, and transferring scalable processes from pre-clinical to validated cGMP ready manufacturing. The team is seeking a highly motivated Laboratory Operations Assistant to coordinate the day-to-day lab operations, ensuring that client projects are progressing, and systems are set-up and maintained according to quality standards and SOPs. This includes, but not limited to, ordering laboratory supplies, calibration of laboratory equipment, maintenance of inventory database, and supporting both scientists and project managers. | 8/16/2022 |
| 6263 | Fulgent Genetics Temple City, CA Lab Technician I Bachelor’s Degree in molecular biology, genetics, or related field. Exp: 1 to 4 years |
The Lab Technician I is responsible for performing clinical laboratory test procedures following standard operating (SOP) and quality assurance (QA) procedures under general supervision. The successful candidate will be a key contributor to a team committed to clinical sequencing and diagnostic test services. | 8/17/2022 |
| 6264 | Personalis Menlo Park, CA Clinical Lab Assistant 1 Bachelor of Science in Biotechnology or related field Exp: 0-1 years |
We are looking for a Clinical Lab Assistant to join our operations team who enjoys troubleshooting and problem solving in a dynamic, team-oriented environment. In this role, you will have the opportunity to participate in the daily activities of the laboratory in order to effectively maximize turnaround time, equipment, and material utilization while adhering to quality technical standards. *Please note, this is a temp to hire opportunity with a typical duration of 3 months working as a temporary worker prior to conversion to employee status. Shift available: Tues to Sat PM (1-9:30 PM) – Training schedule may be different | 8/17/2022 |
| 6265 | Personalis Menlo Park, CA Clinical Lab Associate 1, Extractions BA/BS in a biological discipline Exp: 0-2 years |
This is a 3 month temp to hire position. We have openings for Sun-Thurs (AM or PM).As a team member of our small and growing biotech company, you’ll be integral to our shared mission of enabling precision medicine for cancer treatment. In support of our Clinical Lab Ops, your primary responsibilities will be performing DNA & RNA extractions, related QC, data analysis and other tasks in support of the next generation sequencing services. | 8/17/2022 |
| 6266 | Personalis Menlo Park, CA Clinical Lab Associate 1, Sequencing BA/BS in a biological discipline. Exp: 0-2 years |
As a team member of our small and growing biotech company, you’ll be integral to our shared mission of enabling precision medicine for cancer treatment. In support of our Clinical Lab Ops, your primary responsibilities will be performing next generation sequencing, related QC, data analysis and other tasks in support of the next generation sequencing services. | 8/17/2022 |
| 6267 | Personalis Menlo Park, CA Clinical Lab Associate I BA/BS in a biological discipline. Exp: 0-2+ years |
This is a 3 months temp to hire position. We have Multiple openings on the below teams for swing and day shifts (Tues - Sat or Sun - Thurs). You will participate in the daily activities of the laboratory in order to effectively maximize turnaround time, equipment, and material utilization within budgetary constraints while adhering to quality technical standards. | 8/17/2022 |
| 6268 | Personalis Menlo Park, CA Clinical Lab Associate I, WGS BA/BS in a biological discipline Exp: 0-2 years |
This is a 3 months temp to hire position. We have openings for Swing (Sun - Thurs). Located in Menlo Park, CA, we are seeking a talented and highly motivated Clinical Laboratory Associate to join our Operations Team. Under the direction of the Laboratory Manager, the successful candidate will help grow the Whole Genome and cell free DNA (cfDNA) Operations Sequencing Services Team. You will participate in the daily activities of the laboratory in order to effectively maximize turnaround time, equipment, and material utilization within budgetary constraints while adhering to quality technical standards. Primary responsibilities will be performing and assisting in laboratory tests, processes and analyses according to the laboratory’s standard operating procedures. Candidates for this position should be highly motivated, a team player, and able to thrive in a high-throughput operations environment. | 8/17/2022 |
| 6269 | Pharmaron Germantown, MD Laboratory Technician, Sample Management Bachelor’s degree in related field Exp: 6 months to 1 year |
e are looking for motivated individuals to join our laboratory in Germantown, MD. This is an opportunity for recent graduates to make a real impact in a highly scientific and regulated environment, demonstrate leadership, ambition and the desire to grow with the department. | 8/17/2022 |
| 6270 | Pharmaceutics International Hunt Valley, MD QA Associate Bachelor’s degree in Microbiology or Chemistry. Bachelor’s degree in Microbiology or Chemistry. Exp: one (1) to three (3) years |
Witness and verify the QA functions related to manufacturing of sterile product while adhering to the cGMP ICH and USP/EP/Health Canada guidelines as written -- to ensure that the day-to-day tasks of the Quality Assurance Unit supports the overall business plan while maintaining the highest quality products and ensuring the safety, identity, strength, purity, and quality that the drug is purported to possess. Perform “Line Clearance” and “Cleaning Verification” for manufacturing and packaging operations per established Standard Operating Procedures (SOPs) and Batch/Packaging and Labeling Records’ requirements. Perform in-process sampling, inspections, testing, and batch record reviews during manufacturing and packaging operations as per established SOPs and Batch/Packaging and Labeling Records’ requirements. Perform Acceptable Quality Level (AQL) sampling for in-process and finished product. | 8/17/2022 |
| 6271 | Phitonex Carlsbad, CA Scientist I, Cell Biology Bachelor's degree preferred or equivalent certification/experience in a life science field is required. Exp: 0-2 years |
As part of the Cell Biology R&D team, the Scientist will develop new products that empower our customers to discover and gain a deeper understanding of how cells work and enable research in cell biology, immunology, oncology, and infectious disease. If you can picture yourself in a dynamic and empowering environment where your contributions will have a direct impact on life science research and where you will have the opportunity to learn and develop your career, we encourage you to apply to join our team! | 8/17/2022 |
| 6272 | Phitonex Rockford, IL Production Scientist 1, Biochemistry Bachelor of Science degree in a Biochemistry, Chemistry, Biological Sciences, or other Life Science emphasis. Exp: Entry-Level |
As a new hire in this role you are eligible for a $1,000 Sign-On Bonus! The Production Scientist I, Biochemistry is an introductory manufacturing laboratory position. All work is conducted with an emphasis on safety and within the guidelines and requirements of ISO-regulated/lean manufacturing environment. This position requires working efficiently and effectively to achieve goals relative to safety, quality, delivery, and cost. The Production Scientist I, Biochemistry position will work under the guidance of more senior personnel. | 8/17/2022 |
| 6273 | Phitonex Frederick, MD Scientist I, Cell Biology R&D Bachelor’s degree in Biology, Bioengineering, Biochemistry, or a related subject area Exp: 1-3 years |
You will work as a part of Advanced Cell Models R&D to support ongoing projects within the Thermo Fisher product commercialization process under the Gibco™ brand. You must have experience with cell culture, either immortalized cell lines or primary cells. The candidate should also have familiarity with downstream analyses, including the evaluation of cells via microscopy, Western blot, flow cytometry, or similar techniques. An innovative and curious mentality, attention to detail, and ability to multitask while maintaining a focus on critical projects are essential. | 8/17/2022 |
| 6274 | Phitonex Florence, SC Scientist I - Process R&D BS/BA degree in chemistry or BS in science Exp: 0-3 years |
This is an entry-level opportunity to support the Process R&D efforts at the Florence, SC facility. You will join a team of synthetic organic chemists to support manufacturing of pharmaceutical ingredients at the Florence, SC east site. Many of our products are already in the market serving patients. We work on a variety of projects for existing and new clients with a good combination of routine and challenging work. At this position, you will perform hands-on experimentation and learn skills to run reactions, analyze samples and interpret results. We have a dynamic and fast-paced working environment while keeping a good work-and-life balance. We encourage employees to participate technical discussions and expand their skill sets. | 8/17/2022 |
| 6275 | Phitonex Greenville, NC QC Scientist I (Environmental Monitoring): 12-hour Nights Bachelor’s degree in related discipline preferred, associate degree in a science related field, preferably Biology, minimally required. Exp: Up to 2 years |
Provides routine analyses in a microbiology environment by following standard practices. Follows standard operation procedures as assigned for monitoring in classified environments. Supports internal development and/or manufacturing operations. Makes detailed observations and reviews, documents, and communicates test results. Documenting, reporting and analyzing data in a laboratory setting. Typical shift hours are 6p-6a on a 2-2-3 rotating schedule. | 8/17/2022 |
| 6276 | Phitonex San Diego, CA Scientist I, Chemistry Bachelor of Science or Bachelor of Arts degree, preferably in Biology or Chemistry or equivalent, is required. Exp: 1+ year |
Manufacture in a lab setting following standard operating procedures (SOP). Will apply basic laboratory techniques, calculations, materials measurement, operation of laboratory equipment and record keeping vital to manufacture products in a GMP environment. Wet chemistry formulation, dispense, and lyophilization. Responsible for Batch Data Records, notebooks (if required) and work order documents. Maintain equipment, product inventories and related records as assigned. | 8/18/2022 |
| 6277 | Plex Pharma San Diego, CA Research Associate, Biology & Protein Chemistry BS or MS in molecular and biology, protein chemistry or related field Exp: 1-3 years |
The successful candidate will contribute to drug discovery efforts by performing cloning, expression and purification of protein drug targets, as well as assisting in assay development and characterization of compounds. | 8/18/2022 |
| 6278 | Principia Biopharma Framingham, MA Laboratory Technician, Cell Culture Development Associate’s degree Exp: 1 year |
Join a team dedicated to supporting cell culture process development and other activities within Upstream Mammalian Platform CMC organization located in Framingham, MA. We are looking for an individual that is familiar with sterile technique, cell culture lab equipment and has good laboratory and documentation practices. | 8/18/2022 |
| 6279 | Principia Biopharma Framingham, MA Senior Research Associate, Cell Therapy Flow Cytometry Master’s degree in Biology/Biochemistry or related discipline Exp: 1 – 3 years |
The Senior Research Associate is responsible for executing test methods under control of established procedures. Specifically, performing in-process and release testing of cellular therapies out of our 45 NYA manufacturing facility. Additional functions will include interpretation of data, preparation of test documentation, and management of analytical databases. We are looking for a candidate that is capable of learning quickly with the goal of executing analytical methods and managing assigned test schedules, with excellent communication skills. | 8/18/2022 |
| 6280 | Principia Biopharma Cambridge, MA Associate Scientist, Nanoparticle Development BS in Chemical Engineering, Biomedical Engineering, Chemistry, Material Science, or closely related field Exp: 1+ years |
This position provides a unique opportunity to partake in nanoparticle formulation, process development, and characterization activities with a focus on process scale-up. Additionally, working with an inter-disciplinary team of chemists, biologists and engineers provides an understanding of the drug discovery, pre-clinical research and development paradigm. As such, we are interested in candidates with diverse backgrounds and interests. As part of a nimble, fast-growing team, the individual will have the opportunity to make significant contributions to the company’s mission on a daily basis. | 8/18/2022 |
| 6281 | Khloris Biosciences Mountain View, CA Cell Therapy Manufacturing Technician B.S. degree in biology, biochemistry, bioengineering, or related technical field Exp: 0-5 years |
Khloris Biosciences, Inc. is seeking innovative and highly motivated cell therapy manufacturing technician to join our team. The selected candidate will work closely with lead manufacturing technicians, scientists, participate in project and team meeting, and work in a multidisciplinary environment. The duties of this position will involve supporting a multidisciplinary manufacturing team in developing Khloris cell therapy platforms. The ideal candidate will have hands-on expertise and comprehensive understanding of cell therapy manufacturing processes. | 8/8/2022 |
| 6282 | Lantheus Medical Imaging N. Billerica, MA Manufacturing Technician 4 - 2nd Shift Bachelor Degree in a science related field Exp: 1 – 2 years |
The objective of this position is to perform manufacturing operations required to produce pharmaceutical products in a timely manner compliant with cGMP, OSHA, and other regulatory requirements. Under the direction and on-the-floor guidance of the 2nd Shift Manufacturing Supervisor, the Manufacturing Technician IV will become qualified and independently capable of performing all aspects of internal cold manufacturing operations. Such operations include, but are not limited to, receipt and transfer of materials and components into the manufacturing unit operation, component and equipment cleaning and preparation, operation of automated manufacturing equipment with good aseptic technique, completion of production transactions within the ERP system, completion of paper-based production records and forms in accordance with GDP. | 8/9/2022 |
| 6283 | Lonza Houston, TX Research Associate, Bioassay Services Bachelor’s Degree or Master’s Degree in Biological Sciences Exp: entry level years |
Research Associate, Bioassay Services, performs analytical support, assay development and optimization, and assay qualification. This position is also responsible for writing Method SOPs and Forms. Responsible for writing protocols and reports for Assay Qualification and Assay Validation. Oversees training of QC Analysts on new assays and transferring these assays to QC. Interacts with clients in meetings specifically about Assay Tech Transfer, Qualification and Validation | 8/9/2022 |
| 6284 | Lonza Houston, TX Research Associate Bachelor’s Degree or Master’s Degree in Biological Sciences Exp: entry level years |
Research Associate will support our Process Development and Bioassay Services group. This individual will provide technical support to Scientists and other Research Associates including conducting scientific experiments as well as the tools to conduct and collect data. This individual will also support the Lab Manager and perform common laboratory duties including supply of material, equipment maintenance, and general lab duties. | 8/9/2022 |
| 6285 | Lonza Tampa, FL Lab Technician Bachelor’s Degree in Science Exp: 1 year |
Lonza Tampa is hiring a Lab Technician for our R&D laboratory. The incumbent will carries out the practical work in the laboratory like equipment cleaning, change overs, process execution, or physical testing of materials. Takes over responsibility for lab organization and upkeep with minimal assistance. Uses judgement based on practice and precedence. | 8/9/2022 |
| 6286 | Lonza Houston, TX Lab Assistant Bachelor’s degree in Life Science, Biotechnology, or Bioengineering Exp: 1 year |
Lonza is seeking a highly motivated research associate to support analytical activities, assay development and optimization in the Viral Vector Research and Development team (R&D). This role in entry level and we will train individual to execute assays for characterizing viral vectors and support in assay development activities while supporting team in the lab current projects, while completing daily lab maintenance. | 8/9/2022 |
| 6287 | Lonza Houston, TX Research Associate, Bioassay Services Bachelor’s Degree or Master’s Degree in Biological Sciences Exp: entry level years |
Research Associate, Bioassay Services, performs analytical support, assay development and optimization, and assay qualification. This position is also responsible for writing Method SOPs and Forms. Responsible for writing protocols and reports for Assay Qualification and Assay Validation. Oversees training of QC Analysts on new assays and transferring these assays to QC. Interacts with clients in meetings specifically about Assay Tech Transfer, Qualification and Validation | 8/9/2022 |
| 6288 | Loop Genomics San Jose, CA Service Research Associate B.Sc or M.ScB.Sc or M.ScB.Sc or M.Sc Exp: 1-2 years |
We are looking for an outstanding team player to join our NGS sample prep team and report to the Director of Molecular Biology. The individual will provide next generation sequencing service to our customers that incorporates Loop Genomics's long read technology with Illumina's short read sequencing platforms. This includes applying the standard operating procedure during NGS library preparation, as well as custom solutions tailored to the specific sequencing projects. The individual will also assist in testing and improving the robustness of Loop Genomics’s library preparation kits. This role requires excellent laboratory liquid handling skills and consistent performance of various wet lab operations. The ideal candidate is a dedicated and detail-oriented individual who thrives in a fast-paced work environment, has a solid background in molecular biology techniques, and shares our passion in bringing technology to change the current paradigm of DNA sequencing. | 8/9/2022 |
| 6289 | Loxo Oncology Louisville, CO Research Associate/Associate Scientist, Biophysics BS or MS Exp: 0-3+ years |
Loxo@Lilly's newly formed Drug Discovery group in Louisville, Colorado has an immediate opening for a researcher in Biophysics. The Loxo Drug Discovery group’s mission is to invent life-changing targeted therapies for cancer patient populations that are poorly treated by existing therapies. To that end, we are building a multi-disciplinary team of dedicated drug discovery scientists who are passionate about driving the science forward to create highly selective drugs for known oncogenic drivers. The ideal candidate is self-motivated, responsible, and a productive scientist who enjoys collaborating with biologists, chemists, and assay scientists. In this role, he/she will utilize a variety of assay technologies including mass spectrometry, fluorescence spectroscopy, surface plasmon resonance, and isothermal titration calorimetry to evaluate protein/ligand interactions. Experience in protein purification and characterization is a plus. This position requires excellent people skills, a positive can-do attitude, passion for lab work, attention to detail, and the ability to thrive in a highly interactive, fast-paced, team environment. | 8/9/2022 |
| 6290 | Lubrizol Life Science Health Bethlehelm, PA Associate Scientist Bachelor of Science in a related discipline Exp: 0 – 3 years |
Operating under the general guidance of the Director of DEDD, the Associate Scientist leads formulation efforts in the development of drug eluting devices withing the Bethlehem facility. The Associate Scientist has responsibility for executing product development, from inception to manufacturing of internal and client-based products. | 8/9/2022 |
| 6291 | Lubrizol Life Science Health Midland, MI Chemist B.A. or B.S. in Chemistry preferred Exp: 0-5 years |
The Lab Technician is responsible for all facets of testing, from sample preparation to reporting of results. The majority of the workday is spent in a laboratory setting working with new and used oils, solvents, chemicals and equipment utilized to complete testing. This person is responsible for ensuring safety and good housekeeping practices during daily operations, as well as, operating and maintaining the equipment. | 8/9/2022 |
| 6292 | Lung Biotechnology Manchester, NH Associate Process Engineer, Biomaterials Associate Process Engineer, Biomaterials Associate Process Engineer, Biomaterials Bachelor’s Degree in Arts/Sciences (BA/BS) in materials science, chemistry, chemical, mechanical or biomedical engineering (or equivalent) Exp: 1+ years |
The Associate Process Engineer, Biomaterials (OMG) will be responsible for scaling up and experimenting with large batches of ink to support process and product feasibility goals. This position will also be responsible for periodic quality control (QC) testing. | 8/10/2022 |
| 6293 | Lung Biotechnology RTP, NC Research Associate I/II - Bioscaffolds Research Associate I/II - Bioscaffolds Research Associate I/II - Bioscaffolds Bachelor’s degree in arts/sciences (BA/BS) in life science, engineering, biomedical science Exp: RA I: 1+ years |
Conduct and assist in product development and research efforts for tissue-based regenerative medicine products for treatment of pulmonary hypertension and other lung diseases. More specifically, support decellularization process development and focus on material and functional characterization of lung scaffold and RegenLung construct. | 8/10/2022 |
| 6294 | Lung Biotechnology Manchester, NH Associate Biomedical Engineer / Biomedical Engineer Associate Biomedical Engineer / Biomedical Engineer Associate Biomedical Engineer / Biomedical Eng Bachelor’s Degree in Arts/Sciences (BA/BS) in biomedical, chemical engineering, mechanical engineering, bioengineering or similar/related discipline Exp: 1+ years |
The Biomedical Engineer - Lung Function (OMG) will work on the preclincal team and will support and lead the functional evaluation of 3D printed scaffolds (both cellularized and un-cellularized) and will standardize methods for assessment of performance. This position will work closely with both the cellularization and print process teams of OMG. | 8/10/2022 |
| 6295 | Merieux NutriSciences Gainesville, FL Microbiologist 1 Bachelors preferred Exp: One (1)- 2 years |
The incumbent is responsible for the testing of samples using various microbiological analyses. The incumbent provides analytical support for the lab by ensuring that laboratory procedures are being performed within specified quality guidelines. This position serves as a technical resource and provides ongoing technical support related to method and process implementations. This position spends the majority of time or all of their time in diagnostics. | 8/12/2022 |
| 6296 | Meso Scale Discovery Gaithersburg, MD Bioanalytical Associate I Bachelor’s degree in life sciences, protein sciences, cellular/molecular biology, chemistry, biochemistry, biotechnology, or other related area is req Exp: 1+ years |
The Bioanalytical Associate I is responsible for handling biological samples, reagents, and materials in support of sample testing and assay service projects. This is a laboratory based position whose primary function will be sample management and handling, under direct supervision and direction. The incumbent may also perform protein-based immunoassays on a routine basis with relatively high throughput (2-8 plates per day). The incumbent is expected to adhere to all standard operating procedures and policies established for execution of Bioanalytical studies and sample testing projects under applicable regulatory compliance requirements. | 8/12/2022 |
| 6297 | Moderna Therapeutics Cambridge, MA Research Associate, Nucleic Acid Technology BS or MS in Molecular Biology, Biochemistry, Biology, Chemical Engineering, or closely related field Exp: 1-5 years |
Moderna is seeking a curious, detail-oriented research associate for our Nucleic Acid Technology team. In this laboratory-based position, the individual will participate in the synthesis and analysis of research scale material using novel processes in support of Moderna’s mRNA platform. Implementation of novel processes will require the individual to experiment and optimize to establish new protocols. Laboratory experience with nucleic acids and detailed recordkeeping is essential for this role. Experience with HPLC and mass spectrometry is a plus. The candidate should have a background in biology, chemistry, or chemical engineering. The candidate should enjoy working in a dynamic and innovative environment and be flexible in working both individually and within cross-functional teams to enable cutting-edge nucleic acid research. | 8/12/2022 |
| 6298 | Moderna Therapeutics Norwood, MA Research Associate, Clinical Biomarker Laboratory, Virus Neutralization Assays & Bio-Analytics Bachelor or MSc in vaccine, virology, or related field. Exp: Fresh graduates are encouraged to apply |
Moderna is seeking an agile and motivated Research Associate to join the Clinical Immuno-Assay group to serve as analyst for the virus neutralization assay development, qualification/ validation, and sample analysis to support programs across multiple therapeutic areas. The candidate will need to perform analytical work and maintain clinical testing continuity. The ability to effectively communicate within a project team is expected. Preferably, the candidate has some prior experience in running assay validation and conducting data acquisition on clinical specimen. The candidate should be a collaborative team member and an excellent communicator to support Moderna’s portfolio needs. The individual will work closely with project team members to develop analytical methods and characterization tools in support of our clinical phase studies. The position will report to the group lead of Virus Neutralization Assay. | 8/12/2022 |
| 6299 | Moderna Therapeutics Norwood, MA Research Associate, Analytical Technical Operations BS in Analytical Biochemistry, Chemistry, Organic Chemistry, Chemical Engineering, or a related field Exp: 0-2 years |
We seek a motivated individual with experience in analytical chemistry to support Technical Development. Candidates should have experience with various analytical techniques such as LC, molecular biology, and biophysical characterization. In this laboratory-based position, the individual will oversee operation and troubleshooting of analytical equipment, including LC’s, plate readers and liquid handlers. Experience with lab automation is a plus. The candidate must thrive in a fast pace environment, have a collaborative spirit, and be curious and willing to learn new techniques to push process development forward. | 8/12/2022 |
| 6300 | Moderna Therapeutics Norwood, MA Engineer I, Process Development BS/MS in Chemical Engineering, Chemistry, Biochemical Engineering, Biochemistry or closely related field Exp: 0-3 years |
Moderna is working to develop first-in-class messenger RNA (mRNA) based medicines. We are seeking a Bioprocess scientist or engineer to reside in Moderna’s Technical Development organization in Norwood, MA. Our team’s goal is to envision, pilot, scale, characterize, transfer, and validate robust commercial GMP manufacturing processes. We seek applicants who are proactive, enthusiastic, and show a passion for process development. The successful candidate must be able to work in a fast paced and highly dynamic environment, will have relevant academic and or industrial experience in large molecule bioprocessing (e.g. reactions, mixing, chromatography, tangential flow and/or normal filtration), and will be able to contribute to both process development and commercialization related activities. This role requires close working relationships with Analytical, Manufacturing, Supply Chain, Quality, Regulatory and Program Management functions. | 8/12/2022 |
| 6301 | MP Biomedicals Solon, OH Production Chemist Bachelor of Science in Chemistry, Biochemistry, or Biology Exp: 0-3 years |
The production chemist will be trained in two different product lines: Immunology and Molecular Biology Liquids and will learn and be responsible for a wide variety of product formulation tasks. Such as, following and optimizing production processes while following safety protocols to produce quality research products in a timely fashion to meet customer demand. | 8/12/2022 |
| 6302 | MP Biomedicals Irvine, CA R&D Scientist I Bachelor’s or Master's degree Exp: 0-3 years |
The R&D Scientist I will support the R&D department through Cell Biology associated product development. We are seeking a highly motivated, creative R&D Scientist I with experience in life sciences cell, molecular, and immunology laboratories. This candidate will be expected to lead some projects independently and to work with other scientists in a highly collaborative team environment. Projects may include, but are not limited to, cellular functional assays, cell engineering, protein characterization, sample preparation through homogenizer, DNA and RNA extraction, preparation, and analysis (NGS). | 8/12/0202 |
| 6303 | DPT Laboratories Morgantown, WV Chemist II Bachelor's degree (or equivalent) Exp: 0-2 years |
Key responsibilities for this role include: Perform pharmaceutical testing including, but not limited to, HPLC, GC, TLC, UV, dissolution, and IR spectroscopy. Develop and validate analytical test methods for pharmaceutical products. Critically evaluate and audit data. Write technical analytical reports and procedures. | 8/12/2022 |
| 6304 | Nanosyn Santa Clara, CA Research Associate / Screening and Compound Profiling BS in Biology, Biochemistry or other relevant discipline Exp: 0-2 years |
We are currently seeking a highly motivated screening and compound profiling research associate to join our biology department in Santa Clara, CA. The candidate will play a key role in the organization by being responsible for the planning and timely execution of in vitro biochemical and cell-based assays for Nanosyn’s screening and profiling services. He/She will be responsible for consistently generating high quality data and meeting agreed upon timelines. Applicants must have a strong focus on quality and attention to detail, have the ability to work on multiple projects simultaneously, and be productive both independently and as part of a team. The ideal candidate should have good organizational skills, possess good problem solving, communication and interpersonal skills and to adapt rapidly to new challenges. | 8/12/2022 |
| 6305 | Natera San Carlos, CA Research Associate B.S. degree in molecular biology, related field, or equivalent. Exp: 1 year |
The Research Associate 1 performs research and/or development tasks in collaboration with others. Makes detailed observations, analyzes data, and interprets results. Investigates, creates and develops new methods and technologies for project advancement. Maintains high level of professional expertise through familiarity with scientific literature. | 8/12/2022 |
| 6306 | Nautilus Biotechnology San Carlos, CA Research Associate II Bachelor’s degree in a Life Science field Exp: 1 year |
We are hiring for a Research Associate II to join our growing team. The R&D probe characterization Research Associate II will support the research staff in characterizing affinity reagents using DNA and protein assays. The role will require the candidate to perform affinity measurements, assess data quality and understand why discrepancies may exist between affinity measurement techniques. As the candidate gains understanding of the differences between the assays, they will help nominate which candidate molecules to move forward in the pipeline, providing an opportunity for the candidate’s growth and development into new areas of the organization. | 8/12/2022 |
| 6307 | Nephron Pharmaceuticals West Columbia, SC Analytical Chemist I - Weekend Shift (Fri.-Sun. - 7:00am to 7:00pm & Mon. - 8:00am to 12:00pm) BS or MS in Chemistry, Biochemistry or a related field required Exp: 0-3 years |
Position Summary: Support quality control testing and research and development activities as needed; Assists with additional work duties or responsibilities as evident or required; Performs other duties as assigned or apparent; Relies on instructions and pre-established guidelines to perform job functions; Works under immediate supervision. | 8/12/2022 |
| 6308 | Nephron Pharmaceuticals West Columbia, SC Analytical Chemist I - Second Shift (Sun. - Thurs. - 2:00pm to 11:00pm) BS or MS in Chemistry, Biochemistry or a related field required Exp: 0-3 years |
Position Summary: Support quality control testing and research and development activities as needed; Assists with additional work duties or responsibilities as evident or required; Performs other duties as assigned or apparent; Relies on instructions and pre-established guidelines to perform job functions; Works under immediate supervision. | 8/12/2022 |
| 6309 | Nephron Pharmaceuticals West Columbia, SC Microbiology R&D Analyst I Master’s Degree in Microbiology or other science-related field Exp: 1 - 3 years |
Performs research and develops projects for both established and new products, including, but not limited to, microbiological test method validation/transfer/verification, procedures, investigations, and other non-specified projects or initiatives. Plans, organizes, and manages resources on method validation projects to assure technical quality and schedule adherence. Performs other duties as assigned or apparent. Works with different microbiological techniques and equipment, including but not limited to gram stain, turbidimetric endotoxin testing, liquid particle counter, isolator, bioburden, filtration analysis, sterility testing, aseptic process simulation, and MALDI-TOF. Performs different microbiological tests for R&D Microbiology and QC Microbiology, as needed; also understands and performs routine investigations related to Environmental Monitoring and laboratory testing. | 8/12/2022 |
| 6310 | NGM Biopharmaceuticals South San Francisco, CA Research Associate II / Sr. Research Associate, Antibody Engineering Bachelor/Master's degree in biochemistry, chemistry, or related field Exp: 0-2 years |
We are seeking a highly motivated Research Associate II/Sr. Research Associate to join our Antibody Engineering and Discovery group and contribute to the early drug discovery efforts. The successful candidate will play a critical role in characterization of antibody hits and identification of lead therapeutic candidates using various biophysical platforms | 8/12/2022 |
| 6311 | North Star Medical Technologies Beloit, WI Process Chemist Bachelor’s degree in Chemistry, Chemical Engineering or related physical science/engineering Exp: up to 2 years |
The Process Chemist is responsible for developing and scaling up chemical processes and recommending equipment for the commercial production of NorthStar products. They will work in laboratories and production facilities to develop and test chemical production processes. Processes will include having to work with radioactive materials. Testing may include the development of test methods and working with analytical instruments as required. | 8/12/2022 |
| 6312 | Novartis Carlsbad, CA Clinical Lab Associate Bachelor's degree in technology science or health-related field Exp: Entry-level |
Entry-level laboratory position providing support to clinical testing activities. Responsibilities may include initial intake and registration of patient specimens; handling and pre-analytical processing of patient specimens; data entry and quality check of patient information and pre-analytical data entered into the laboratory information system; slide preparation; and sample management/storage. | 8/12/2022 |
| 6313 | Novartis Cambridge, MA BS/MS Research Scientist, Oncology Drug Discovery - Biotherapeutics MS with basic knowledge in immuno-oncology, immunology or cell and molecular biology Exp: 0-4 years |
We are seeking a highly passionate and motivated research scientist to join our team at Novartis Oncology Biotherapeutics in Cambridge, MA. This position is ideal for someone who is creative, highly collaborative, result-oriented and wishes to combine their curiosity about oncology, cancer immunology and drug discovery to save patients’ lives. In this role, you will have the opportunities to contribute to exploratory and innovative biotherapeutic drug discovery for cancer using a variety of different assays to independently support research in this area. The successful candidate will become a crucial part of a dynamic and multidisciplinary group to interact with other functional groups and to understand the process of preclinical drug discovery, that will eventually transform the lives of cancer patients. | 8/12/2022 |
| 6314 | Norvartis Carlsbad, CA Laboratory Assistant (Digital Pathology Solutions) BS/BA with scientific emphasis preferred Exp: no experience required |
As a Laboratory Assistant at Navigate, you will perform and assist with laboratory operations under GCP/GLP/CLIA regulations to support clinical trial sample testing. | 8/12/2022 |
| 6315 | Novartis Cambridge, MA Synthetic Chemistry Research Scientist (BS or MS) BS or MS degree in synthetic organic chemistry Exp: 0 to 5+ years |
We would like to welcome a highly motivated, scientifically curious, and innovative synthetic chemist to our Synthesis Technologies Team within Global Discovery Chemistry (Cambridge, MA). You will join an energizing and collaborative research environment working alongside colleagues who are committed to improving human health through the discovery of transformative medicines. | 8/12/2022 |
| 6316 | Novavax Gaithersburg, MD Research Associate I (Contract to Hire) Bachelor’s degree in biological science, molecular biology, immunology Exp: RA II: 1-3 years |
We are seeking Research Associate II to join our Clinical Immunology department in Gaithersburg, MD. This role is a contract to hire position. This individual will play an important role in clinical testing activities related clinical samples including assay development and qualification. In addition, individual will be expected to generate accurate high throughput clinical data following qualified assays using high throughput clinical testing. | 8/12/2022 |
| 6317 | Novavax Gaithersburg, MD Lab Technician, Upstream Process Development (Contractor) – NanoFlu BS in chemical engineering, biochemistry, molecular biology, microbiology or related area Exp: 0-2 years' |
Collaborate and coordinate with colleagues in buffer preparation, broth clarification, and upstream material hand-off to downstream process development for additional purification steps Performs washing and decontamination of glassware and distributing to appropriate locations within the laboratories. Maintains glass washing facility, including picking up and cleaning of glassware May sterilize glassware and other items using an autoclave or depyrogenation oven Maintains laboratory equipment, inventory levels, and organization of laboratory supplies Maintains record keeping for duties performed Assist in shipping and receiving of supplies Performs other related duties as required Setup, monitor, and harvest bioreactor runs up to the 20L scale to support upstream and downstream process development efforts | 8/12/2022 |
| 6318 | NovoBiotic Pharmaceuticals Cambridge, MA Associate Scientist - Microbiologist B.S. or M.S. in Biology/Microbiology Exp: 0 to 5 years |
We are currently seeking to hire microbiologists with 0 to 5 years of experience. The successful applicant will perform microbiology lab work and data analysis to discover previously unculturable microorganisms from soil and marine environments and their identification by molecular taxonomy methods. Additional tasks will include detection of antibiotic production from these organisms and in vitro characterization of their properties, such as spectrum of activity, mechanism of action, resistance development and cytotoxicity | 8/12/2022 |
| 6319 | Noxilizer Hanover, MD Research and Development Laboratory Scientist Bachelor’s degree in Biology, Biotechnology, Biomedical Engineer, Material Science or related field Exp: 1 year |
The R&D Lab Scientist is responsible for performing, documenting and reporting microbiological sterilization studies for Noxilizer’s customers. Noxilizer’s customers range from Fortune 500 pharmaceutical, biotech and medical device companies to start-ups that are in the US, Europe and Asia. These studies are the first critical step in the customer’s evaluation of nitrogen dioxide sterilization and their product, as well as an important revenue-generating area for the company. The R&D Laboratory Scientist will join a high-performing team of experts to solve sterilization challenges while they grow their skills for future career opportunities. | 8/12/2022 |
| 6320 | Nucelis San Diego, CA Senior Research Associate/Research Specialist, Strain Development MS degree Exp: 0-5 years |
We are looking for a highly motivated individual who will be part of the Strain Development team to create a robust high throughput strain engineering and testing platform in oleaginous yeast. You will work with molecular biologists, fermentation scientists, process engineers and analytical chemists to create and identify microbial strains with the highest potential to produce sustainable microbial products. | 8/12/2022 |
| 6321 | Hikma Cherry Hill, NJ Quality Lab Associate I, Micro - * 1500 sign on bonus * BS/BA Degree in Microbiology or Biology Exp: 0-2 years |
Perform functions within the Microbiology Laboratory and/or conduct critical microbiological analysis on test articles from all stages of the manufacturing process from incoming raw materials to finished goods. The duties also include equipment maintenance and LIMS management | 8/1/2022 |
| 6322 | Hikma Cherry Hill, NJ Quality Lab Associate I, Micro - * 1500 sign on bonus * BS/BA Degree in Microbiology or Biology Exp: 0-2 years |
Perform functions within the Microbiology Laboratory and/or conduct critical microbiological analysis on test articles from all stages of the manufacturing process from incoming raw materials to finished goods. The duties also include equipment maintenance and LIMS management | 8/1/2022 |
| 6323 | Hikma Columbus, OH Scientist I, QC Microbiology 1st Shift - 1946 B. S. in scientific field required Exp: One to three years |
To ensure that all products, raw materials and the environment for production are microbiologically acceptable while ensuring regulatory compliance standards and release times are met. | 8/1/2022 |
| 6324 | Hillrom Marion, NC Quality Engineer 1 B.S. in technical area (mechanical, electrical, chemical, biological, etc.) Exp: 0 - 2 year |
Ability to perform standalone repeat and/or routine validations with little or no guidance. Ability to provide requirements for change control based on procedural requirements Be able to assist, present, defend and communicate with external auditors and others validations or projects in which you lead or participated. Assist or lead process improvement projects (scrap reduction, defect reduction, etc.) with little or no guidance. Can work with other support groups (production, quality, laboratory, etc.) in a collaborative manner. Display a solid technical understanding of engineering principles and procedures (e.g. CAD and its application or scheduling a series of technical tasks utilizing software-based tools and/or specialties such and chemical, industrial or biological). Assists in the preparation and participation in technical reviews and responsible for organizing data and preparing appropriate documentation for assigned projects. Provide assistance to management or other engineers during design, installation, qualification and/or process monitoring. Provide technical reports and/or data driven analysis after training.Ability to perform standalone repeat and/or routine validations with little or no guidance. | 8/1/2022 |
| 6325 | Hillrom Round Lake, IL Quality Lab Associate I Bachelors degree in Chemistry or Science related degree Exp: 6 months or more |
The Quality Lab Associate I will be located at the Drug Delivery Chemistry Laboratories, Round Lake, IL. The Position encompasses the biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs. This is a first shift position but will be required to work on weekends to support training of analysts and to support projects and/or production, as required. A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials. | 8/1/2022 |
| 6326 | i2O Therapeutics Boston, MA Wet Lab Associate BS in biochemistry, chemistry, chemical engineering or a related science field Exp: 1 year |
The Associate will primarily assist in and conduct, as appropriate, synthesis and analysis of compounds, preparation of samples for analysis, assays of chemical and biological samples, preparation of samples for shipping, and general upkeep of the lab and supplies. Primary responsibilities include supporting scientists in setting up, monitoring and analyzing samples from a variety of studies including drug solubility, stability and permeability. Other activities include ordering and receiving supplies, preparing ionic liquids and conducting standard assays on the synthesized ILs. They will also be trained in performing ELISA or other assays and HPLC or LCMS sample preparation and operation. The technician will assist in new investigative projects as needed for platform development. The position will work under modest supervision and in compliance with Lab Central regulations and company SOPs and guidance. | 8/2/2022 |
| 6327 | IDEAYA Biosciences South San Francisco, CA Research Associate, ex vivo Pharmacology BA/BS or MS (Research Associate) Exp: 1+ years’ |
IDEAYA is seeking a South San Francisco based Senior Research Associate for our Pharmacology and Toxicology group. This individual will play a key role in the development and execution of preclinical models to understand the efficacy and PK/PD relationships of our small molecule agents under development for the treatment of cancer. The ideal candidate will enjoy working with multi-disciplinary teams in a fast-paced environment and will have the passion to contribute to the discovery and development of novel therapeutic agents for cancer patients. | 8/2/2022 |
| 6328 | IDEAYA Biosciences South San Francisco, CA Research Associate/Senior Research Associate, Translational Sciences BS or MS degree in cell/molecular biology or Oncology Exp: 1 year |
We are seeking a highly-motivated, well-organized and laboratory-focused Research or Senior Research Associate (RA/SRA) that will play a key role in supporting project needs for Translational Research in an oncology small molecule development team. The successful candidate will work in a multidisciplinary team and contribute to the generation of novel therapeutics for the treatment of cancer. Position level will commensurate with experience. | 8/2/2022 |
| 6329 | Illumina San Diego, CA Research Associate - Material Science Research Associate - Material Science Research Associate - Material Science BS or MS degree in Chemistry (Physical Chemistry, Material Science, Analytical Chemistry). Exp: 0+ years |
We are seeking a motivated individual for a Research Associate position in the Research and Technology Development group based at our San Diego headquarters. As part of the Materials and Applied Surface Science group, you will play an integral role in developing new sequencing and array technologies and related applications. You will be part of multidisciplinary teams solving complex problems and investigating new research areas. With the rapidly evolving nature of our research work, the candidate should be able to adapt to a wide range of techniques and methods used in life sciences. | 8/2/2022 |
| 6330 | Illumina San Diego, CA Research Associate 1 - Material Science Research Associate 1 - Material Science Research Associate 1 - Material Science BS or MS degree in Chemistry (Physical Chemistry, Material Science, Analytical Chemistry). Exp: 0+ years |
As part of the Materials and Applied Surface Science group, you will play an integral role in developing new sequencing and array technologies and related applications. As the company moves fast, so does the technology we use, and the candidate will have to be adaptable to a wide range of techniques and methods used in life-sciences. | 8/2/2022 |
| 6331 | Illumina San Diego, CA Integration Research Associate 2 Integration Research Associate 2 Integration Research Associate 2 B.S./M.S. in Bioengineering, Chemical Engineering, Biochemistry, Analytical Chemistry, Biology, or equivalent B.S./M.S. in Bioengineering, Chemical En Exp: 0 - 2 years |
The Integration Research Associate 2 will work in a dynamic, team-oriented environment and help create genomic analysis tools used in the leading edge of research. This position will participate in the development of high quality, robust products through the integration of hardware, software, and chemistry components. They will execute test plans in order to optimize product performance. | 8/2/2022 |
| 6332 | Illumina San Diego, CA Research Associate, Assay Development Research Associate, Assay Development Research Associate, Assay Development Bachelor’s or Master's degree in biochemistry, molecular biology, genetics, genomics or related field. Exp: 0 - 5 years’ |
As a Research Associate within Illumina’s Assay Development team, you will work as part of multi-disciplinary Research & Development group to support sample preparation in the generation of sequencing based assays for clinical oncology applications. In this role you will primarily be responsible for preparing and testing samples to support assay development and optimization. | 8/2/2022 |
| 6333 | IMMY Norman, OK Antigen Technician I Bachelor’s degree in Microbiology, Biology, Biochemistry, or a related field Exp: 0-1 years |
The role of the Antigen Technician I is to produce high quality fungal and bacterial antigens to manufacture IMMY diagnostics. This technician will succeed in this role by gaining knowledge and understanding the history, processes, and goals of the BSL3 laboratory and cultures, including optimizing antigen reactivity, and increasing a more robust raw material inventory. This person must have high attention to detail, good aseptic technique, and lab skills. Under moderate supervision, they will perform various tasks such as media preparation, various fungal and bacterial species cultivation, harvesting and filtration of antigens, and post-quantitative and qualitive testing while keeping accurate and complete records using our ERP system. The Antigen Technician I may assist in various process validations and is encouraged to generate ideas to improve processes or product quality. | 8/2/2022 |
| 6334 | IMMY Norman, OK Antibody Technician I Bachelor’s degree in Microbiology, Biology, Biochemistry, or a related field Exp: 0-1 years |
The role of the Antibody Technician I is to produce high quality monoclonal and polyclonal antibodies to manufacture IMMY diagnostics. This technician will succeed in this role by gaining knowledge and understanding the history, processes, and goals of the Cell Culture Lab, including optimizing goat serum reactivity, and increasing a more robust antibody inventory. This person must have high attention to detail, good aseptic technique, and lab skills. Under moderate supervision, they will perform various tasks such as media preparation, hybridoma cultivation, harvesting and purification monoclonal antibodies, polyclonal goat antibody maintenance, and post-quantitative and qualitive testing while keeping accurate and complete records using our ERP system. The Antibody Technician I may assist in various process validations and is encouraged to generate ideas to improve processes or product quality. | 8/2/2022 |
| 6335 | Inova Diagnostics San Diego, CA Research Associate I Bachelor’s degree; Bachelor of Science degree in Biology, Microbiology, Cellular Biology, Biochemistry, or similar field of study. Exp: 1-2 years |
This position assists in developing current and future Inova Diagnostic product lines by performing laboratory activities to assist in developing new assays and/or identifying potential new biomarkers. This position works under the supervision of the R&D management team. It performs lab activities of limited scope, following good laboratory documentation practices and in accordance with Standard Operating Procedures and other Research and Quality System requirements. | 8/2/2022 |
| 6336 | Inova Diagnostics San Diego, CA Chemist I- Bioflash Manufacturing Bachelor's degree B.A. or B.S. or equivalent in the biological or related sciences Exp: 1-2 years |
Participates in the preparation of autoimmune diagnostic products, utilizing the Bioflash technology platform, following established procedures. Major duties include Bioflash bead and reagent preparation activities and the preparation of controls and conjugates for the Bioflash product lines. | 8/2/2022 |
| 6337 | Inova Diagnostics San Diego, CA Research Associate I Bachelor’s degree; Bachelor of Science degree in Biology, Microbiology, Cellular Biology, Biochemistry, or similar field of study. Exp: 1-2 years |
This position assists in developing current and future Inova Diagnostic product lines by performing laboratory activities to assist in developing new assays and/or identifying potential new biomarkers. This position works under the supervision of the R&D management team. It performs lab activities of limited scope, following good laboratory documentation practices and in accordance with Standard Operating Procedures and other Research and Quality System requirements. | 8/2/2022 |
| 6338 | Inova Diagnostics San Diego, CA Research Associate I Bachelor’s degree; Bachelor of Science degree in Biology, Microbiology, Cellular Biology, Biochemistry, or similar field of study. Exp: 1-2 years |
This position assists in developing current and future Inova Diagnostic product lines by performing laboratory activities to assist in developing new assays and/or identifying potential new biomarkers. This position works under the supervision of the R&D management team. It performs lab activities of limited scope, following good laboratory documentation practices and in accordance with Standard Operating Procedures and other Research and Quality System requirements. | 8/2/2022 |
| 6339 | Integral Molecular Philadelphia, PA Research Associate – Job ID# 05052022 (Fulltime with weekend coverage) bachelor’s degree in biology, bioengineering, or a related field is required Exp: 1–2 years |
To support our growth, we seek a Research Associate I, who will work with a dedicated group of scientists on the production and characterization of antibody therapeutics. This position will involve training Monday through Friday for approximately three months, and then will transition to a position (approximately 9am to 5pm) that will require you to work at least one weekend day (Tue-Sat or Thurs-Mon). | 8/2/2022 |
| 6340 | Integral Molecular Philadelphia, PA Research Associate (Job ID# 090306) bachelor’s degree in biology, bioengineering, or a related field is required Exp: 1–2 years |
To support our growth, we seek a Research Associate I, who will work with a dedicated group of scientists on the development and commercialization of biomedical technologies. | 8/2/2022 |
| 6341 | Integral Molecular Philadelphia, PA Research Technician (Job ID# 062319) Associate or Bachelor’s degree in Biology, Chemistry, medical technology or related field Exp: 6 months – 2 years |
To support our growth, we seek a Research Technician to join our Membrane Proteome Array research team. | 8/2/2022 |
| 6342 | Intellia Therapeutics Cambridge, MA Senior Research Associate Genomic Innovation and Screening MS in Molecular Biology, Biotechnology, or related field Exp: 0-2 or more years |
As a Senior Research Associate in the Genomic Innovation and Screening team, you will be primarily responsible for planning and executing cell-based screening assays to characterize and quantify gene editing events under the guidance of a scientist. If you are a strong, independent problem-solver, detail-oriented with a strong technical background in mammalian cell cultures, and enjoy working in cross-functional teams, this is the role for you. | 8/2/2022 |
| 6343 | Invitae San Francisco, CA DNA Extraction Laboratory Trainer Bachelor’s degree in clinical laboratory studies or equivalent science related studies Exp: 1+ years |
We're looking for a passionate individual that enjoys developing training and competency programs, instructing and guiding others with varying levels of experience, and driving quality and continuous improvement. As a part of our Technical Team and in partnership with the Extraction Operations Lead, you will ensure successful expansion and execution of our lab processes through the facilitation of training, competency and validation programs, coaching team members to be tomorrow’s technical leaders, and challenging yourself to delve into opportunities for professional development. This role requires on-site work at our San Francisco location as well as opportunity to work overtime and off-schedule days as needed to accommodate training schedules. | 8/2/2022 |
| 6344 | Invitae San Francisco, CA DNA Extraction Technician Bachelor’s degree in clinical laboratory studies or equivalent science related studies Exp: 1+ years |
SCHEDULE: Thur-Mon, 7:00 am - 3:30 pm Thur-Mon, 3:00 pm-11:30 pm We're looking for passionate laboratory technicians who will support high complexity laboratory testing on patient specimens across various assays and platforms. This role will be performing quality control and quality assurance procedures while complying with all applicable local, state and federal laboratory requirements. The work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask and be flexible with tasks and schedules, and the ability to work independently in a team environment. This role requires on-site work at our San Francisco location as well as ability to work overtime and off-schedule days as needed. | 8/2/2022 |
| 6345 | Invitae San Francisco, CA Engineering Technician Bachelor degree in an engineering or science field preferred Exp: 1 – 2 years |
SCHEDULE: Sun - Thurs (Hrs TBD but possible differential pay!) We are looking for a passionate and driven Engineering Technician to join our Equipment Engineering Team who can come in and own the day to day equipment tasks which maintain regulatory compliance, equipment states and a high functioning lab environment. This individual will be able to seamlessly interface with production and engineering teams to drive forward task completion. | 8/2/2022 |
| 6346 | Invitae San Francisco, CA Engineering Technician Bachelor degree in an engineering or science field preferred Exp: 1 – 2 years |
SCHEDULE: Sun - Thurs 10:30am - 7:00pm + differential pay! We are looking for a passionate and driven Engineering Technician to join our Equipment Engineering Team who can come in and own the day to day equipment tasks which maintain regulatory compliance, equipment states and a high functioning lab environment. This individual will be able to seamlessly interface with production and engineering teams to drive forward task completion. | 8/2/2022 |
| 6347 | Invitae Iselin, NJ Extraction Technician Bachelor’s or Master's degree in Medical Technology, Biology, Chemistry, Biochemistry or related life science Exp: 1 years |
SCHEDULE: Monday - Friday, 8:30 AM - 4:30 PM EST hours Our Iselin (Metropark), NJ operations team is looking for a passionate and focused Extraction Laboratory Technician I to join invitae and support high-complexity laboratory testing on patient specimens across various assays and platforms. The extraction team member will partner with the Extractions Lead to continuously improve daily extraction operations at our Metropark Laboratory. | 8/2/2022 |
| 6348 | Invitae San Francisco, CA Reagent Manufacturing Technician Bachelor's degree in Biochemistry, Chemistry, or a related science discipline Exp: 1+ years |
Multiple Openings! Schedule: Tues – Sat 3:00 pm-11:30 pm OR Sun - Thurs 3:00 pm-11:30 pm We're looking for a passionate Reagent Manufacturing Technician to join our Clinical Laboratory Operations team in San Francisco. You will work with complex laboratory testing (next-generation DNA sequencing) on patient specimens including all steps from specimen processing to data analysis, performing quality control and quality assurance procedures, and complying with all applicable local, state and federal laboratory requirements. The work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask and be flexible with tasks and schedules, and the ability to work independently in a team environment. | 8/3/2022 |
| 6349 | Iovance Biotherapeutics Philadelphia, PA Aseptic Manufacturing Technician (4 x10 hour work week) Minimum B.S. degree in biology, biochemistry, bioengineering, or related technical field, or equivalent industry experience. Exp: 0-5 years |
As this person will be a key member of the autologous cell therapy manufacturing program, a background in cell culture, aseptic gowning and qualification, and ISO class 5 cleanroom operations is required. | 8/3/2022 |
| 6350 | Cambridge Isotope Laboratories Andover, MA Chemist I MS in Chemistry Exp: 0-3 years |
Cambridge Isotope Laboratories, Inc. (CIL) is seeking a Chemist I to join our production team based onsite in our Andover, MA location. As the leading company in a niche scientific market, CIL works with cutting edge researchers in clinical diagnostics, metabolic research, proteomics, environmental testing, protein discovery, drug development, metabolomics, and industrial research. CIL's growing customer base spans academia, pharmaceutical and industry, enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. Under the supervision of a group leader or supervisor, the Chemist I will work alongside an experienced scientist executing syntheses of isotopically labeled (13C, 15N, 18O and D isotopes) targets utilizing highly detailed SOPs and procedures. | 8/3/2022 |
| 6351 | Cambridge Isotope Laboratories Tewksbury, MA QA Associate I BA/BS within a Science or Quality concentration preferred Exp: 0-2 years |
The Quality Assurance Associate I is responsible for the quality of several new and existing active pharmaceutical ingredients (APIs) and medical device components in a GMP/ISO Environment. | 8/3/2022 |
| 6352 | Janssen Pharmaceuticals Cambridge, MA Associate Scientist M.S. Exp: 1-2 years |
We are seeking an Associate Scientist to join the TS team within the Immunology therapeutic area. This candidate will assist in designing and conducting biomarker assay strategies for the advancement of clinical development programs across the Immunology portfolio, with a focus on inflammatory and autoimmune diseases. The successful candidate will possess strong organization and communication skills and demonstrate the ability to design, shape, implement novel experiments and interpretation of data. | 8/3/2022 |
| 6353 | Janssen Pharmaceuticals San Diego, CA Associate Scientist I Master's Degree in Pharmacology, Neuroscience, or Biology Exp: 1 to 3 years |
We are seeking a highly motivated Associate Scientist with in-vitro neuropharmacology experience to join our Neuroimmunology Discovery research team in La Jolla, CA. The candidate will be passionate about the discovery and development of novel therapeutics for CNS disorders. Experimental work will be the core job function and as such the ideal candidate will spend close to full time at the bench generating data. It is critical that the successful candidate enjoys bench science, is scientifically curious, is self-motivated, and can demonstrate a high level of operational efficiency. Strong interpersonal skills, the ability to interact well with peers and collaborators, and strong written and oral communication skills are vital to success in this role. | 8/4/2022 |
| 6354 | Janssen Pharmaceuticals San Diego, CA Associate Scientist I, Neuroimmunology Master's Degree in Pharmacology, Neuroscience, or Biology Exp: 1 to 3 years |
We are seeking a highly motivated Associate Scientist with in-vivo neuropharmacology experience to join our Neuroimmunology Discovery research team. The candidate should be passionate about the discovery and development of novel therapeutics for CNS disorders. Experimental work will be the core job function and as such the ideal candidate will spend close to full time at the bench generating data. It is critical that the successful candidate enjoys bench science, is scientifically curious, is self-motivated, but also a strong standout colleague, and can demonstrate a high level of efficiency. Strong interpersonal skills, the ability to interact well with peers and collaborators, and strong written and oral communication skills are vital to success in this role. To be successful in the position, the candidate must be organized, and practice good laboratory principles including detailed notebook entry of experiments. | 8/4/2022 |
| 6355 | Janssen Pharmaceuticals Malvern, PA Associate Scientist, Biotherapeutics Drug Product Development (1 of 2) BS in Chemical, Bioengineering or related field Exp: 0-2 years |
The Associate Scientist in Drug Product Development (DPD) will work independently and in conjunction with appropriate teams to support program/project needs. The candidate will also help design and perform process development and engineering studies in support of DP fill-finish activities for biotherapeutics (e.g. mAbs, fusion proteins, multispecifics, etc). | 8/4/2022 |
| 6356 | Janssen Pharmaceuticals Malvern, PA Associate Scientist, Large Molecule Drug Product Development M.S. degree in Engineering (Biomedical, Bioengineering, Chemical, Electrical or Mechanical) Exp: 1 year |
The Associate Scientist in Large Molecule (LM) Drug Product Development (DPD) will work independently and in conjunction with development teams to support program/project needs. The candidate will also independently be accountable to lead, design, perform, and analyze studies in the development and engineering space in support of process and fill-finish activities for large molecules (e.g. monoclonal antibodies, fusion proteins, bi-specifics, gene therapies, cell therapies etc). | 8/4/2022 |
| 6357 | Janssen Pharmaceuticals Spring House, PA Associate Scientist II, Immunology Discovery Master’s degree in Immunology/Cell Biology or equivalent Exp: 1 year |
Janssen Research & Development, L.L.C., a Johnson & Johnson Company, is hiring a full-time Associate Scientist II position in the Immunology – Discovery group and will be located in Spring House, PA. | 8/4/2022 |
| 6358 | JRF Global Audubon, PA Scientist I/ Entry Level Chemist Bachelor of Science or advanced degree from an accredited college or university in chemistry or other science-related field Exp: 1-3 years |
Set up experiments under the guidance of a Scientist II and/or Team Lead Operate equipment, observe and log the progress of experiments Promptly submit experimental data / findings to the supervisor Promptly inform the supervisor of any problems encountered during the experiments. Assist in data entry in various formats and verify accuracy of data entry Assist in writing drafts of Protocols and Reports Provide a daily update on the progress, findings and results for each experiment. Compile the data as directed by the supervisor Check the quality and accuracy of the data before submission to the supervisor | 8/4/2022 |
| 6359 | KBI Biopharma Louisville, CO Research Associate I/II B.S. degree Exp: 0-2 years |
Open position available in the biophysical characterization core of the rapid analytics testing group. Responsible for analytical testing of client samples. Testing may include using client-based methods or some method development. Ideal candidate is able to quickly and accurately generate results. Technical writing skills are a plus. | 8/4/2022 |
| 6360 | KBI Biopharma Durham, NC Research Associate II B.S. in a related field Exp: 1-4 years |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. | 8/4/2022 |
| 6361 | Enzo Life Sciences Farmingdale, NY Associate Scientist BA/BS in Chemistry or related field Exp: 1+ years |
This position will be assisting the Manufacturing Team specifically with chemistry products and the in process testing required for regular small molecules. | 7/25/2022 |
| 6362 | Eurofins Viracor BioPharma Services Cambridge, MA Research Associate (In - Vivo) Bachelors degree or Associates Degree Exp: 1-2 years |
Under general supervision, performs a wide range of assigned research experiments with efficiency, accuracy and attention to detail. Performs in-life experiments including injections by conventional routes (IV, SC, IP, PO, IM) necropsy and tissue collection, blood sampling (submandibular and cardiac puncture) and general health evaluations. Comply with IACUC and AALAS guidelines on the care of use of experimental animals in research. Analyze biological samples using a variety of techniques, including ELISA activity assays and other kit based assays. Maintain meticulous records of experimental data and observations in laboratory notebooks in strict accordance with corporate guidelines.Under general supervision, performs a wide range of assigned research experiments with efficiency, accuracy and attention to detail. | 7/25/2022 |
| 6363 | Eurofins Viracor BioPharma Services San Diego, CA Research Associate I Research Associate I Research Associate I Bachelor’s degree in life sciences or related discipline Exp: 1+ years |
Become your most extraordinary self! Our team is intensely proud to be a major provider of services and products to the drug discovery research industry. Join Eurofins Beacon Discovery part of the Eurofins Discovery ™ group of companies serving global clients in the Pharma and Biotech industries. Work alongside industry experts and collaborate with team members to directly and positively impact human health worldwide! We have a philosophy to support work life balance, career progression opportunities and offer many benefits such as formal mentoring programs, tuition reimbursement, extensive career training programs, competitive health benefits, paid time off and 10 annual paid holidays*. Become your most extraordinary self! Our team is intensely proud to be a major provider of services and products to the drug discovery research industry. | 7/25/2022 |
| 6364 | Eurofins Viracor BioPharma Services South San Francisco, CA Research Associate, Molecular Biology Bachelor's degree in a science related discipline Exp: 0 to 3 years |
This is a technical position within a Gene Therapy group in South San Francisco to perform viral vector production in support of novel discovery programs. This job will involve assisting in all stages of Adeno-associated virus (AAV) production and purification. Key responsibilities will be establishing and maintaining relevant protocols, cell culture expansion and maintenance, transfections, sample filtration and purification, and data recording and entry. The candidate will be able to contribute to new technology development and concept generation. The ideal candidate will have a background in production and/or purification of proteins or other biomolecules (especially viral vectors) and some experience in an industry setting (especially CRO work). | 7/25/2022 |
| 6365 | Eurofins Viracor BioPharma Services Cambridge, MA Research Associate Candidate must have a degree in Cell and Molecular Biology, Biochemistry, Pharmaceutical, or other biological/analytical discipline Exp: 0-2 years |
Supports viral vector process development by providing analytical testing on DNA, ELISA, cell based platform within agreed upon turn-around; Demonstrate good understanding of ongoing programs and data generated in relation to the program; Troubleshoots issues as needed with supervision; Monitors assay performance to ensure GLP compliance | 7/25/2022 |
| 6366 | Eurofins Viracor BioPharma Services Fremont, CA Research Associate - Molecular Biology Bachelor’s degree Exp: 1-3 years |
Become your most extraordinary self! Our team is intensely proud to be a major provider of services and products to the drug discovery research industry. Join Eurofins DiscoverX Products, LLC part of the Eurofins Discovery ™ group of companies serving global clients in the Pharma and Biotech industries. Work alongside industry experts and collaborate with team members to directly and positively impact human health worldwide! | 7/25/2022 |
| 6367 | Eurofins Viracor BioPharma Services Cambridge, MA Research Associate, Analytical Development Bachelor’s Degree in related science Exp: 0-2+ years |
Seeking an energetic and dependable analyst to perform routine testing to support process development and help progress programs through the pipeline. This individual will focus on molecular biology assays with a development opportunity to cross-train and support cell-based, potency, flow cytometry, separations and biophysical methods as well. This analyst will interface with many departments and projects necessary to complete tasks in a timely manner. | 7/25/2022 |
| 6368 | Exelixis Alameda, CA Scientist I, Compound Repository Scientist I, Compound Repository Scientist I, Compound Repository BS in related discipline Exp: one year |
The Scientist I, HTS is responsible for assisting in the development and completing the assay execution of both high throughput screening (HTS) campaigns in 1536-well plate format and weekly screening campaigns in 384-well plate format using the appropriate automation. | 7/25/2022 |
| 6369 | Exelixis Alameda, CA Scientist I (Pharmacology, Formulation) Master’s degree in a related chemistry, pharmaceutical sciences, biochemistry, biology discipline Exp: zero or more years |
The successful and highly motivated candidate will support the in vivo pharmacology research program to perform pre-formulation work, develop formulation study, execute analytical test methods, organize the data and summarize related reports. | 7/25/2022 |
| 6370 | Exelixis Alameda, CA Scientist I (Lead Discovery) Scientist I (Lead Discovery) Scientist I (Lead Discovery) BS in related discipline Exp: one year |
The Scientist I, HTS is responsible for assisting in the development and completing the assay execution of both high throughput screening (HTS) campaigns in 1536-well plate format and weekly screening campaigns in 384-well plate format using the appropriate automation. | 7/25/2022 |
| 6371 | Exelixis Alameda, CA Scientist II (Tumor Biology) Scientist II (Tumor Biology) Scientist II (Tumor Biology) BS/BA degree in related discipline Exp: one year |
We are looking for a Scientist for our Tumor Biology Department. The successful and highly motivated candidate will evaluate the activity of small molecule inhibitors in cell-based assays for oncology drug discovery. Comfortable in a dynamic and energetic team-based environment, the ideal candidate will reliably execute experiments, interpret and analyze results. Good lab practicing and multitasking are required. This job will require the candidate to have good organization, communication and teamwork skills as well as flexibility and versatility to meet tight deadlines in a dynamic, fast-moving environment. | 7/25/2022 |
| 6372 | Exelixis Alameda, CA Scientist II (ADC Biology) Scientist II (ADC Biology) Scientist II (ADC Biology) Bachelor’s degree in pharmacology or cancer biology or closely related discipline Exp: one (1) year |
Discovery Biotherapeutics is seeking an experienced, self-motivated Scientist II to provide in vitro pharmacology support for the advancement of the biologics portfolio at Exelixis. The successful candidate must have strong pharmacology background in cancer as he/she will support preclinical activities of ongoing and new biologics projects in antibody drug conjugates and bispecific antibodies. | 7/25/2022 |
| 6373 | Exelixis Alameda, CA Scientist II (Oncology Discovery) Scientist II (Oncology Discovery) Scientist II (Oncology Discovery) BS/BA degree in related discipline Exp: one year |
We are looking for a Scientist for our Tumor Biology Department. The successful and highly motivated candidate will evaluate the activity of small molecule inhibitors in cell-based assays for oncology drug discovery. Comfortable in a dynamic and energetic team-based environment, the ideal candidate will reliably execute experiments, interpret and analyze results. Good lab practicing and multitasking are required. This job will require the candidate to have good organization, communication and teamwork skills as well as flexibility and versatility to meet tight deadlines in a dynamic, fast-moving environment. | 7/25/2022 |
| 6374 | FloDesign Sonics Jaffrey, NH Process Engineer Bachelor’s Degree in Engineering (e.g., Manufacturing, Industrial, Mechanical, Design) Exp: 1+ years |
At Millipore Sigma the Process Engineer will work in a dynamic environment supporting the manufacture and testing of high purity filters with a focus on quality, process control/improvements, electro-mechanical assembly, and material handling. The successful candidate will be an enthusiastic team player with high energy and strong engineering skills. | 7/25/2022 |
| 6375 | FloDesign Sonics Danvers, MA Quality Engineer I Bachelor’s Degree in Engineering, Biology, Chemistry, or related field Exp: 1+ years |
As a Quality Engineer at MilliporeSigma in our Danvers, MA, production site, you play a key role in the success of the Quality and Manufacturing organizations. | 7/25/2022 |
| 6376 | FloDesign Sonics Tempe, AZ Analytical Chemist Master’s degree in Physics, Chemistry, or other Science discipline Exp: 1+ years’ |
EMD Electronics in Tempe, AZ is seeking a Chemist to join our Analytical Technology group. This group performs analysis and characterization of trace metals and nanoparticles used in CMP slurries for the semiconductor fabrication industry. | 7/25/2022 |
| 6377 | FloDesign Sonics St Louis, MO Associate Scientist Master’s Degree in Biology or Chemistry or Life Science field Exp: 1+ years |
At MilliporeSigma, as an Associate Scientist you will conduct immunoassays and Research & Development related activities within the Life Science business. This individual could be responsible for several roles focusing on new product development, product validation, troubleshooting, and Operations support for key biological reagents. This is an excellent opportunity to gain experience in groundbreaking, high sensitivity assay technologies and new product development processes in the biotechnology industry and will report to the R&D Manager. | 7/25/2022 |
| 6378 | FloDesign Sonics Rockville, MD Associate Scientist 2 Bachelor’s degree in scientific field (i.e., Biology, Chemistry, etc.) Exp: 1+ years |
In this role, you will perform a wide variety of routine tasks to support the virus production team in the growth of regulatory compliant virus banks, under the oversight of the Scientist. You will be responsible for performing cell culture activities, virus growths, virus titration assays and virus decontamination procedures. The ability to maintain effective working relationships with support services, scientists and all laboratory personnel are critical for success in the role. | 7/25/2022 |
| 6379 | Flagship Biosciences Broomfield , CO Analyst I Bachelor’s degree in a scientific field and Exp: 0‐2 years |
The Analyst I, with team support, is the first line scientific resource responsible for delivery of analytical services, to include: generation of images, performance of image analysis related tasks, contribution to new analytical techniques and procedures, dispersal of project components to appropriate cross departmental resources, and providing feedback to drive project goals. The Analyst I must be eager to learn from and interact with colleagues at all levels of our organization, have a positive attitude and look for ways to continuously improve. The right fit for this position views collaboration and frequent communication as invaluable tools for building relationships and successfully accomplishing the goals. The Analyst I must be consistently flexible and be willing to adapt to rapidly changing priorities. | 7/27/2022 |
| 6380 | Galatea Surgical San Diego, CA Research Associate II Bachelor’s or Masters degree, in Biology or related scientific discipline. Exp: One to two years' |
The Research Associate II performs routine and complex laboratory tasks and procedures relevant to custom products and services in the Custom Technology Team. The Associate will perform a variety of routine experimental protocols and procedures to fulfill custom manufacturing requirements that include, but are not limited to formulations, experimental design, product testing/analysis, and results reporting. The Associate will work independently within generally defined procedures and practices in selecting methods and techniques for obtaining results. The Associate will observe and comply with safety standards and procedures and assist in general laboratory maintenance. Direction is both verbal and written. | 7/27/2022 |
| 6381 | Galatea Surgical San Diego, CA R&D Reagent Research Associate BS or BA degree in Molecular Biology, Chemistry, Biochemistry, or related subject area. Master’s degree preferred. Exp: 1 year |
BD is seeking a Reagent Research Associate to work within a team that develops new point-of-care assays for human in vitro diagnostic use. The Reagent Research Associate supports various R&D assay development teams and is principally responsible for the formulation, organization, and quality control of assay raw materials, amplification master mixes, buffers, and consumables. The associate applies good laboratory practice and analytical skills to manage the overall reagent inventory, and material output and works with other team members to resolve technical challenges. Works under the direction of Senior Reagent Scientists or above. | 7/27/2022 |
| 6382 | Genentech Carlsbad, CA RESEARCH ASSOCIATE I B.S. in Biochemistry, Molecular Biology, Analytical Chemistry or a related field Exp: 0 - 3 years |
You will execute a range of molecular biology and bioanalytical procedures, reagent preparation, and laboratory duties under supervision. You will investigate, adapt or modify experimental methods and technologies for project advancement. A unique opportunity to leverage your background and skills in molecular diagnostics to enhance and build your career by working cross-functionally. An exciting career opportunity where your contributions will impact business opportunities through successful completion of projects. | 7/27/2022 |
| 6383 | GenScript Piscataway, NJ Associate Research Scientist, Sequencing Team Master degree in molecular biology related field Exp: 1 year |
We are looking for an associate research scientist for the Sequencing lab. This position will be focusing on high throughput DNA sequencing workflow during the gene synthesis process. | 7/28/2022 |
| 6384 | GenScript Redmond, WA Research Associate Bachelor's degree in molecular biology, chemistry, biochemistry, pharmaceutical science, chemical engineering or related field, Master is preferred Exp: 0-5 years |
GenScript is looking for a highly motivated and scientifically rigorous individual to join our RNA team for RNA delivery formulation and new RNA product research and development as Research Associate. This position will focus on developing novel lipid nanoparticle formulations for RNA delivery. | 7/28/2022 |
| 6385 | GenScript Piscataway, NJ Associate Research Scientist in Automated Gene Synthesis Team Master degree in molecular biology related field Exp: 1 year |
We are looking for an automation power user for the automated gene synthesis team. This position will be focusing on high throughput automated liquid handling and colony picking/ culturing during the gene synthesis process | 7/28/2022 |
| 6386 | Ginkgo Bioworks Boston, MA Cell Culture Associate (Cambridge Location) Bachelor’s degree Exp: 1+ year |
Coordinate with program teams to fulfill cell requests with a dedication to delivering quality work; Execute all aspects of mammalian cell culture for both suspension and adherent cells, including media preparation, culture initiation, propagation, and cryopreservation; Perform assays such as cell count, viability, doubling time, light microscopy, and expression of cell lineage markers by flow cytometry; Independently troubleshoot problems and propose solutions related to cell culture, diagnostic/QC assay design, and execution; Coordinate with teammates for material and task handoffs in order to deliver high-quality, trusted work; Maintain accurate experiment and inventory records in various internal databases; Establish and maintain a clean cell culture laboratory by practicing aseptic technique, adhering to equipment cleaning guidelines, and routinely testing and monitoring equipment and culture sterility; Execute internal development projects to increase capacity and onboard new capabilities for the Mammalian Operations team | 7/28/2022 |
| 6387 | Ginkgo Bioworks Boston, MA Cell Culture Associate (Seaport Location) Bachelor’s degree Exp: 1+ year |
Coordinate with program teams to fulfill cell requests with a dedication to delivering quality work; Execute all aspects of mammalian cell culture for both suspension and adherent cells, including media preparation, culture initiation, propagation, and cryopreservation; Perform assays such as cell count, viability, doubling time, light microscopy, and expression of cell lineage markers by flow cytometry; Independently troubleshoot problems and propose solutions related to cell culture, diagnostic/QC assay design, and execution; Coordinate with teammates for material and task handoffs in order to deliver high-quality, trusted work; Maintain accurate experiment and inventory records in various internal databases; Establish and maintain a clean cell culture laboratory by practicing aseptic technique, adhering to equipment cleaning guidelines, and routinely testing and monitoring equipment and culture sterility; Execute internal development projects to increase capacity and onboard new capabilities for the Mammalian Operations team | 7/28/2022 |
| 6388 | Ginkgo Bioworks Boston, MA Research Associate – Assay Development BS or MS in biology, biochemistry, bioengineering, pharmacology, or equivalent Exp: 1-2 years |
If you have interest in learning how to use cutting edge automation and software to understand, engineer and operationalize biology, perhaps a role as an HTS assay developer would be a good fit for your career. Ideally, you have experience in the development & optimization of biochemical assays and microbial plate culture. As an assay developer, you will design and execute laboratory experiments, generate & interpret data supporting the development of new processes and assays, and execute high-throughput screens. Other responsibilities will include learning about and applying new technical and scientific advances to your work, troubleshooting, data analysis, and reporting. Assay developers interact with and learn from many other teams at Ginkgo, so if you enjoy interdisciplinary work, assay development could be a great fit for you! | 7/28/2022 |
| 6389 | Ginkgo Bioworks Boston, MA Research Associate II, Molecular Biology BS or MS in biology, microbiology, genetics, or equivalent Exp: 1+ years |
We are seeking an inquisitive Research Associate II to join the Build team to help us run and improve our yeast genome engineering service. You will be responsible for amplifying, purifying and transforming DNA to create new strains for our program team. You are the ideal Build operator if you love working closely with a team in a fast paced environment to deliver high quality processes. We need your enthusiasm for accuracy and yeast biology, to help us meet our mission of making biology easier to engineer. Please consider applying even if you don\'t have all of the qualifications. | 7/28/2022 |
| 6390 | Global Pharma Tek Houston, TX Research Assistant II Bachelor’s Degree or Master’s Degree in Biological Sciences Exp: entry level years |
Client is seeking a highly motivated research associate to perform analytical support and assay qualification in the viral vector Research and Development team (R&D). The successful candidate will be proficient in viral vector characterization assays; perform assays transfer to process development team (PD); be able to analyze bioprocessing data, responsible for writing reports for Assay Qualification and Assay Validation. | 7/28/2022 |
| 6391 | Global Pharma Tek Salt Lake City, UT Scientist 1, Analytical Chemistry Development Associates degree or higher in a STEM major (Examples: Chemistry, biology, microbiology, biotechnology, biomedical engineering). Exp: 1-5 years |
Provide technical skill, analytical testing, and engineering support for design and development activities for various medical device products. Support current products in roles of quality, research & development, pilot-scale manufacturing, supply continuity, and cost improvement. Focus will be on in vitro testing using biological materials. An understanding / training in biology is a plus. Execute technical and cross-functional project | 7/28/2022 |
| 6392 | Gossamer Bio San Diego, CA Contract Research Associate, Biology B.Sc. in cell and molecular biology or related field Exp: 1-2 years |
This is for a contract role through end of 2022. We are seeking a highly motivated scientist/research associate to join the Biology Team to cover for leave of absence. This position will require excellent attention to detail and follow-through on the execution of established protocols as well as the opportunity to participate in the assay development process. The successful candidate will demonstrate a strong commitment to the rigor of scientific research within an industry setting as well as creativity in the form of critical thinking required for the interpretation of experimental data. | 7/28/2022 |
| 6393 | GRO Biosciences Cambridge, MA Research Associate/Sr RA, Chemistry Expansion MS degree (or BS/BA degree in biology, microbiology, biotechnology, biological engineering, or related field Exp: 1 year |
GRO Biosciences (GRObio) is hiring an RA/Sr RA with bench experience in molecular biology to advance the company’s recoded organism technology. Recoded organisms enable GRObio to generate revolutionary products of unprecedented structural and chemical diversity. With the tools at GRObio, you’ll be able to propose, develop, and implement completely differentiated solutions to longstanding, critical problems. The selected candidate for this position will work within the Chemistry Expansion division, enabling the scalable incorporation of new amino acids into proteins. Major job responsibilities include development and screening of translation machinery for new amino acids, and general engineering of ribosomal translation. Day-to-day activities include design and execution of experiments in conjunction with other team members. Diligence, transparent communication, and record keeping will be critical skills to enable success in this position. Your creativity and ingenuity will be crucial to driving GRObio’s research priorities optimizing strain performance and expanding the amino acid alphabet to create differentiated products. | 7/28/2022 |
| 6394 | GlaxoSmithKline Collegeville, PA Associate Analytical Scientist Bachelor’s degree Exp: 1-3 years |
As an Associate Analytical Scientist, you will progress analytical aspects of projects, utilizing your technical expertise as part of a product development and wider matrix teams. The candidate may engage with project teams and other stakeholders for various projects under different stages of development. The candidate may interact with other labs, internal and external to GSK, to support the training and transfer of analytical methods. | 7/28/2022 |
| 6395 | GlaxoSmithKline Collegeville, PA Associate Scientist BS degree in Pharmaceutics, Biology, Biochemistry, Chemistry, Chemical Engineering, or related scientific discipline Exp: 1 year |
As an Associate Scientist, you will join the Technology Advancement and Portfolio/Platform Support team within the Process Engineering and Analytics department of the Drug Product Development organization within the GSK R&D. You will primarily support drug product manufacturing process development using the small-scale capabilities, platform initiatives, combination product development, support technology transfers, and new technology implementation for new products in the pipeline. | 7/28/2022 |
| 6396 | GlaxoSmithKline King of Prussia, PA Biopharm Manufacturing Associate II BS/BA in life sciences/engineering or computer science/information systems. Exp: no previous experience |
As a Biopharm Manufacturing Associate II, you will perform production operations including fermentation or cell culture operations, preparation of solutions, chromatographic separation, filtration and concentration operations, autoclave and parts washing of process assemblies, and area cleaning/upkeep. Will be responsible for completing daily manufacturing tasks, and increasing competency in different production areas over time. Will participate in safety and compliance initiatives, as well as investigations. Will engage in the GSK Production System to continuously improve safety, quality, and schedule/cost performance. | 7/28/2022 |
| 6397 | GlaxoSmithKline Collegeville, PA Associate Scientist - Analytical BS or MS in Chemistry Exp: 1+ year |
As an Associate Analytical Scientist, you will progress analytical aspects of projects, utilizing your technical expertise as part of a product development team working with many partner groups. This role will provide YOU the opportunity to contribute to analytical development and to progress YOUR career. | 7/28/2022 |
| 6398 | GlaxoSmithKline Collegeville, PA Associate Scientist, Biology (Upper Providence, PA) Bachelor’s Degree in Biological Sciences (such as Cell Biology, Immunology, Oncology or Molecular Pharmacology) Exp: one year |
As an Associate Scientist, you will develop assays in primary cells and cell lines for immunology and oncology programs for use in high-throughput screening and mechanistic studies. This is an exciting, lab-based role that will allow the individual to contribute to early drug discovery programs through validation of novel targets and new chemical entities. The successful candidate is expected to be effective in designing and executing experiments at the highest possible scientific standard, be highly flexible and productive, and possess positive communication skills. | 7/28/2022 |
| 6399 | Harpoon Therapeutics South San Francisco, CA RESEARCH ASSOCIATE, PROTEIN PURIFICATION Bachelors Exp: 1-5 years |
We are seeking a highly motivated individual who enjoys detail-oriented technical work, can manage diverse responsibilities in the lab, and thrives in a fast-paced work environment. As an integral member of the Protein Science group, this individual will work closely with other team members within Protein Science and partner with other functional areas in the organization. The ideal candidate will have strong technical aptitude for lab and instrumentation work, and a flexible problem-solving mindset | 7/29/2022 |
| 6400 | Heska Des Moines, IA Technician I, II or III, Bacterins Bachelor’s Degree in a science or bio-technology field. Exp: 1 year |
The Bacterins Technician I, II or III will work under the close supervision of the Bacterins supervisor to foster the growth of bacterial cultures through fermentation and cell media preparation while maintaining a sterile environment. This position requires the ability to multi-task and follow standard operating procedures. Position level will be based on experience. | 7/29/2022 |
| 6401 | Champions Oncology Rockville, MD Research Technician I, Surgical Services Research Technician I, Surgical Services Research Technician I, Surgical Services BS degree in biology, pharmacology, or related field Exp: 1 year |
Support in vivo oncology studies in mice as a member of the Surgical Services team. Duties and responsibilities are: Handle, restrain, and provide care for all animals; Observe animals for general health and overall well-being; Receive, characterize and orthotopically or heterotopically surgically implant tissue samples; Provide perioperative and intraoperative animal care; Conduct tumor volume measurements and sample collection for in vitro characterization; Perform preparation activities, including collection tube labeling and room set-up; Perform blood collection, processing and sample storage; Perform various subcutaneous injections; Collect, document, and maintain tissue samples within database as well as the tumor bank; Conduct and record data in compliance with Standard Operating Procedures (SOPs); Record data using laboratory information management systems; Work weekend and holidays as needed | 7/18/2022 |
| 6402 | Champions Oncology Rockville, MD Research Technician I, Study Services BS/MS degree in biology, pharmacology, or related field Exp: 1 year |
As a Research Technician in Study Services, you will support in vivo oncology studies in mice. Additional duties and responsibilities include: Perform in-life technical procedures, handle, restrain, and provide care for all animals; Observe animals for general health and overall well-being; Administer therapeutic agents by various routes; Provide animal welfare assessments, including body weight and tumor volume measurement; Allocate animals to study and non-study groups; Provide preoperative animal care; Euthanize animals as directed in study protocols and directives; Read study protocols and extract pertinent information; Perform study preparation activities including collection tube labeling and room/BSC set-up; Record data using laboratory information management systems; Work weekends and holidays on rotating basis | 7/18/2022 |
| 6403 | Champions Oncology Rockville, MD Research Technician, Necropsy BS degree in biology, pharmacology, or related field Exp: 1 year |
Primary objective: to support the in vivo oncology studies in mice as well as properly euthanize animals in accordance to the company standards and regulations. | 7/18/2022 |
| 6404 | Companion Medical Memphis, TN Microbiologist-Sterilization I Bachelor's degree in Science or technical field Exp: 0+ years |
In this exciting role as a Microbiologist-Sterilization I you will have responsibility to work on assignments that are complex in nature where judgment and initiative are required in resolving problems and making recommendations. Provides input to Supervisor of Microbiology regarding sterilization, testing and technical issues. Works with the contract sterilizers to maintain sterilization cycles using either Gamma Sterilization or Ethylene Oxide Sterilization in accordance with all industry, Federal and international guidance documents/regulations. Interacts with the Regulatory, Quality, Packaging and R&D Engineering in Memphis to maintain the microbiological specifications and test plans necessary to ensure compliance with the overall Quality Requirements. Assists with microbiological and sterilization issues affecting manufacturing. Serves as consultant for laboratory on technical issues. Develops procedures for laboratory testing. Moderate supervision | 7/18/2022 |
| 6405 | Companion Medical Brooklyn Park, MN Microbiologist-Sterilization I Bachelor's degree in Science or technical field Exp: 0 years |
In this exciting role as a Microbiologist/Sterilization I you will have responsibility to support and improve the sterility assurance program for Medtronic's Extra Corporeal Therapies device portfolio. You will focus on the sterilization process, cleanroom technology, and general microbiology for products produced at the Brooklyn Park, Minnesota site. In this position, you will be responsible for monitoring the sterility assurance program and driving timeliness of critical compliance imperatives such as requalifications and product lifecycle change management tasks. This role will also collaborate with other Medtronic global sterility assurance partners to harmonize best practices for cleanroom, microbiology, and sterilization methodologies. | 7/18/2022 |
| 6406 | Companion Medical Fridley, MN Analytical Instrument Specialist Bachelor's in Chemistry, Biology, Engineering or other Science or technical field. Exp: 0+ years |
In this exciting role as an Analytical Instrument Specialist you will have the responsibility for performing routine instrument qualification and maintenance for the Chemistry and Microbiology Laboratories. The candidate will be required to perform planned preventative maintenance and requalification activities. In addition, they will also be expected to perform non-routine instrumentation troubleshooting activities and revise Instrument Operating Procedures (IOPs) to ensure that all maintenance, calibration, and training activities are properly documented and governed. This individual will work in conformance with company policies and current Good Manufacturing Practices, Good Lab Practices (GLP), regulatory requirements and standards to meet quality and accuracy requirements. | 7/18/2022 |
| 6407 | Companion Medical Mounds View, MN Materials Engineer I Bachelor's Degree in materials, chemical, biomedical or mechanical engineering Exp: 0+ years |
This position will support product and materials development for new and released product, ensuring product safety and reliability through the direction and execution of characterization testing. This will include providing problem solving, materials laboratory testing and data analysis in support of new and existing implantable biomedical devices and systems. Biocompatibility and biostability testing, as well as documenting product equivalence through appropriate characterization testing will also be included. | 7/18/2022 |
| 6408 | Companion Medical Mounds View, MN Software Engineer I Bachelor’s degree in Software Engineering, Computer Science, or related technical field. Exp: 1+ years |
As a Software Engineer I in the Cardiac Rhythm Management (CRM) R&D Software Organization, the individual will operate in all phases and contribute to all activities of the software development and verification process. The CRM Medtronic Application Services (MAS) team leverage various software technologies to create, enhance, and maintain Web/Mobile based Patient Management Software System used by our clinicians and patients. The CRM MAS team is looking for a proactive, self-starting, strong software development engineer. | 7/19/2022 |
| 6409 | Companion Medical Mounds View, MN Reliability Engineer I Bachelors degree in Engineering, Science or technical field Exp: 0 years |
The Reliability Engineer will work in a fast-paced environment, partnering closely with Design/R&D, manufacturing, and Regulatory Affairs. This role serves as a technical representative for the Reliability function, ensuring full compliance of the final product. | 7/19/2022 |
| 6410 | Cook Biotech West Lafayette, IN Biocompatibility Scientist Master's degree in Toxicology, Biology, Biomedical Engineering, Material Science, or related field required Exp: 1 year |
The Biocompatibility Scientist at Cook is responsible for assessing the safety of devices and related materials, assisting with writing risk assessments of medical devices, and ensuring the Cook device testing program is compliant to national and international regulatory guidelines. | 7/19/2022 |
| 6411 | CooperSurgical Tucson, AZ Blood/Tissue Sample Processing Technician I - Tucson, AZ Bachelor’s degree in one of the biological, chemical, or physical sciences OR Bachelor’s degree in a different science Exp: 1 year |
Position Summary: The Blood/Tissue Sample Processing Technician I (Hematology) is responsible for analyzing and documenting test results from our cord blood and cord tissue processed samples using standard hematology techniques as dictated by our quality management system while maintaining the highest quality services possible. This position is also responsible for releasing raw materials, supporting the analytical and processing equipment maintenance program, and providing our internal customers with technical expertise while maintaining the highest quality services possible. | 7/19/2022 |
| 6412 | Covaris Woburn, MA Research Associate – Applications Development Master’s Degree in biology, chemistry, biomedical engineering, or biochemistry Exp: 0-2 years |
This hands-on position offers an exciting opportunity in the life sciences to discover, develop, and evaluate new product ideas, enhancements to existing products, or strategic product extensions, and translate research into usable and marketable products. This position involves collaboration in a multi-disciplinary team composed of biologists, chemists, and mechanical and electrical engineers. This position will function as a member of the Applications Team reporting to a Senior Applications Scientist. | 7/19/2022 |
| 6413 | Crown Bioscience San Diego, CA Research Associate I, In Vivo Oncology Research Associate I, In Vivo Oncology Research Associate I, In Vivo Oncology Bachelor’s Degree in a scientific discipline Exp: One year |
In Vivo Research Associate I position is to provide support on In Vivo studies within the In Vivo Pharmacology group meeting Company's goals, objectives and quality standards. | 7/19/2022 |
| 6414 | Crown Bioscience San Diego, CA Research Associate I, In Vivo Oncology Research Associate I, In Vivo Oncology Research Associate I, In Vivo Oncology Bachelor’s Degree in a scientific discipline Exp: One year |
The In Vivo Research Associate I position is to provide support on In Vivo studies within the In Vivo Pharmacology group meeting Company's goals, objectives and quality standards. | 7/19/2022 |
| 6415 | Crown Bioscience San Diego, CA Research Associate I, Autoimmune & Inflammatory Diseases, Pre-Clinical Associate's degree or Bachelor's or Master's degree in Biology, Biotechnology or other relevant area of scientific discipline Exp: 1-2 year(s) |
The purpose of the Inflammation and Immunology Research Associate I position is to perform primarily in vivo animal studies within the Inflammation and Immunology group in support of the Company's goals and objectives. | 7/19/2022 |
| 6416 | Crown Bioscience San Diego, CA Research Associate I, Cancer Biology & Immunology Bachelor's degree in Biology, Biotechnology or other relevant area of scientific discipline. Exp: 1‐ 2 years |
The purpose of the Cancer Biology & Immunology Research Associate I is to provide support with in vitro client studies and help with in vivo studies aligned with Company's goals, objectives and quality standards. | 7/19/2022 |
| 6417 | Crown Bioscience San Diego, CA Research Associate I, Cell Support Research Associate I, Cell Support Bachelor's degree in Biology, Biochemistry or related area. Exp: 1-2 years |
The purpose of the Research Associate I is to provide support with in vitro client studies and help with in vivo studies aligned with Company's goals, objectives and quality standards. | 7/19/2022 |
| 6418 | CryoLife Kennesaw, GA R&D Engineer I BS Degree in Biomedical or Mechanical Engineering Exp: 0 - 2 years |
Advance the development of novel medical devices from initial concept through in vivo characterizations. The position will focus on the prototyping, characterization, testing, and refinement of subcomponents of medical devices. | 7/19/2022 |
| 6419 | CryoLife Kennesaw, GA Process Engineer Bachelor’s degree in Engineering (Mechanical, Chemical, Biomedical, Industrial or related field of engineering) Exp: 0-2 years |
Responsible for providing process engineering support for all product manufacturing departments. Supports manufacturing operations to ensure consistent adherence to the standard operating procedures and business continuity. Initiates process improvement initiatives to improve the efficiency of current manufacturing processes, as well as develop new processes to improve manufacturing efficiency. Supports new product launches by collaborating with other functional areas and providing process engineering expertise during the implementation of processes or equipment. | 7/19/2022 |
| 6420 | Culture Biosciences South San Francisco, CA Lab Technician Associates/Bachelors Exp: 0 year |
Culture Biosciences is hiring for multiple Lab Technicians to support our lab operations, prepare media and run assay testing on client samples. This is an excellent opportunity to learn more about the inner workings of our cloud lab environment, gain valuable experience with operations, media prep, and wet lab skills. We’re motivated to hire those who are eager to learn and excited by the technology we have developed. | 7/20/2022 |
| 6421 | Cyprotex Watertown, MA Research Associate and/or Research Assistant - Toxicology BS/ MS in a relevant bio scientific discipline Exp: 0-2 years |
The team is looking for a highly motivated Research Associate and/or Research Assistant that will be responsible for routine screening of compounds in various in vitro toxicology assays | 7/20/2022 |
| 6422 | Cytovance Oklahoma City, OK ANALYTICAL DEVELOPMENT ASSOCIATE BS/MS in a life science field Exp: BS: 1+ years; MS: 0+ years |
The AD Associate position develops, optimizes, and qualifies analytical methods for biopharmaceutical products. The associate also supports drug development departments, such as Purification Department and Cell Culture Department, by performing analytical testing. | 7/20/2022 |
| 6423 | Cytovance Oklahoma City, OK PD ASSOCIATE - UPSTREAM - MICROBIAL Bachelor’s degree in a life science field Exp: 0-3 years |
The Process Development Associate I conducts laboratory experiments as part of development and/or demonstration of processes related to cell expansion (mammalian or microbial) of biopharmaceutical products. The Associate also participates in activities related to the maintenance and upkeep of the Process Development Lab. | 7/20/2022 |
| 6424 | Demetrix Berkeley, CA Associate Scientist – Plate Model Development Bachelor of Science degree in biological system engineering, biochemistry, microbiology, or related field Exp: 0 to 2 yr |
You will be part of the High Throughput & Process Engineering team and play a key role in the development of novel microbial strains. You will be part of an interdisciplinary team of fermentation/DSP scientists and engineers, automation engineers, software engineers, analytical chemists, and molecular biologists working to rapidly develop microbial strains to produce natural product medicines . In this role, you will work in a highly collaborative fashion with strain and fermentation engineers to screen novel microbial strains and processes in a high throughput manner. This includes designing and executing experiments, analyzing results, troubleshooting deviations, maintaining a high standard of data integrity, and clearly communicating findings cross-functionally. | 7/20/2022 |
| 6425 | DiaCarta Richmond, CA Research Associate S. degree in molecular biology or a related field Exp: 0-2 |
DiaCarta is seeking a highly motivated, independent, and interactive Research Associate to join the R&D function in the company. The new team member will participate in R&D activities with the goal of developing and launching new qPCR, NGS, and branched DNA tests for IVD cancer diagnostics applications. The successful candidate will have outstanding attention to detail, enjoy working in a fast-paced multidisciplinary team environment, and have exceptional hands-on laboratory skills. DiaCarta is a rapidly growing company, so the candidate must be highly motivated and committed to launching their career in an innovative area of molecular diagnostics. This is a full-time role in Richmond, and you will be reporting to the Senior Scientist. | 7/20/2022 |
| 6426 | DiCE Molecules South San Francisco, CA Research Associate/Sr. Research Associate, In Vitro Pharmacology B.S. degree in biochemistry, biology, or a related field Exp: 1-4 years |
The successful candidate will be responsible for planning and independently performing experiments using a wide range of in vitro assays and technologies. These will include biochemical/biophysical and mammalian cell culture assays, and will expand over time. This person will support cutting-edge small molecule discovery through their data and analysis within a growing multidisciplinary team. | 7/20/2022 |
| 6427 | Distributed Bio S. San Francisco, CA Research Associate 1 - In Vivo PK Bachelor’s Degree (B.S./B.A) or equivalent in a scientific related discipline. Exp: Zero to three years |
The individual in this position will be involved in all aspects of studies supporting the biotechnical services group. This position is hands-on with responsibilities including, but not limited to animal husbandry, animal handling and restraint, administration via various routes, clinical observations, sample collection and processing, and accurate data collection. | 7/20/2022 |
| 6428 | Distributed Bio S. San Francisco, CA Research Associate I - In Vivo, CNS 1 1 1 1 Bachelor’s Degree (B.S./B.A) or equivalent in a scientific related discipline. Exp: Zero to three years |
The individual in this position will be involved in all aspects of studies supporting the biotechnical services group. This position is hands-on with responsibilities including, but not limited to animal husbandry, animal handling and restraint, administration via various routes, clinical observations, sample collection and processing, and accurate data collection. | 7/20/2022 |
| 6429 | Distributed Bio Ashland, OH Research Assistant 1 (Bioanalytical Chemistry) Bachelor’s degree (B.A. / B.S) or equivalent in laboratory science or related discipline Exp: Zero to two years |
We are seeking a Research Assistant I for our Safety Assessment Group site located in Ashland, Ohio. Generate and record data with minimal supervision in the performance of studies. Responsible for handling and processing samples, and performing accurate data collection and reporting. Perform laboratory tasks by various basic methods | 7/21/2022 |
| 6430 | Distributed Bio Mattawan, MI Research Analyst 2 - Bioanalytical Bachelor’s degree (BA/BS) or equivalent experience. Exp: 1 year |
We are seeking an Research Analyst 2 for our Bioanalytical Chemistry team at the site located in Mattawan, MI. Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP’s and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents. | 7/21/2022 |
| 6431 | Distributed Bio Spencerville, OH Research Technician Assistant (Entry Level) Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months to 1 year |
Performs technical tasks in the conduct of in vivo research studies or support services in accordance with good animal welfare practices. Prepares, collects and records research data and specimens in compliance with applicable regulations and SOPs. We are seeking an experienced Research Technician I for our InVivo (InLife) Team within our Safety Assessment site located in Spencerville, OH. The following are responsibilities related to the Research Technician 1: The Research Technician 1 will collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods. We are looking for 1st and 2nd shift. 2nd shift does include 10% pay differential M-F 2:30pm-11pm. 1st shift 7am-330pm w/ rotating weekend/month & rotating holidays. | 7/21/2022 |
| 6432 | Distributed Bio S. San Francisco, CA Research Associate I - In Vivo, CNS 1 1 1 Bachelor’s Degree (B.S./B.A) or equivalent in a scientific related discipline. Exp: Zero to three years |
The individual in this position will be involved in all aspects of studies supporting the biotechnical services group. This position is hands-on with responsibilities including, but not limited to animal husbandry, animal handling and restraint, administration via various routes, clinical observations, sample collection and processing, and accurate data collection. | 7/21/2022 |
| 6433 | EAG Laboratories San Diego, CA Cell Biology Associate Bachelor’s degree in biology, biochemistry, molecular biology or similar discipline Exp: 1 or more years |
Eurofins Lancaster Laboratories PSS is searching for a Cell Biology Associate Associate to work in San Diego, CA. Our client is looking to expand its capabilities in biochemical and immunological assays applied to immunology/immunogenicity. We are looking for a highly motivated and agile biochemist. Your contributions may include independently design and perform experiments with the goal of understanding and assessing immunogenicity of biological drugs, and ultimately to generate datasets to inform predictive models of antigen-specific immune response. | 7/21/2022 |
| 6434 | EAG Laboratories San Diego, CA Molecular Biology Associate B.S. in Biological sciences (Molecular Biology, Biotechnology, Immunology, Biochemistry, or similar field) Exp: 1-3 years |
Eurofins Lancaster Laboratories PSS is searching for a Molecular Biology Associate to work in San Diego, CA. | 7/21/2022 |
| 6435 | EAG Laboratories San Diego, CA MSAT Engineer Bachelor's degree in chemistry, microbiology, biology, engineering, computer science, or other related degree concentration Exp: One year |
Applies GMP/GLP in all areas of responsibility, as appropriate; Demonstrates and promotes the company vision; Regular attendance and punctuality; Compliance - Stay current with client, regulatory, validation, IT, and e-record compliance regulations, and requirements. Ensure projects are completed in compliance with existing quality systems. Provide support to implement new quality systems and programs; Research - Assist with research of instrumentation with information obtained from vendors, manuals, and other resources to introduce duplicate/similar instruments and software. Assist with integration of instrumentation into existing data center environments and workflows; Technical Writing - Author validation deliverables in accordance with established validation program. Assist with developing/enhancing instrumentation procedures. Training - Provide guidance and coaching within a team environment. Provide training to technical groups; Validation Support - Accurately update validation program components and maintain LIMS instrument database entries. Perform periodic review for chambers and compile and assist with periodic review of computerized systems. Generate monitoring, trending, and departmental reports. Perform routine project close out activities. | 7/21/2022 |
| 6436 | EAG Laboratories San Diego, CA Research Associate I Bachelor’s degree in life sciences or related discipline Exp: 1+ years |
Our team is intensely proud to be a major provider of services and products to the drug discovery research industry. Join Eurofins Beacon Discovery part of the Eurofins Discovery ™ group of companies serving global clients in the Pharma and Biotech industries. Work alongside industry experts and collaborate with team members to directly and positively impact human health worldwide! We have a philosophy to support work life balance, career progression opportunities and offer many benefits such as formal mentoring programs, tuition reimbursement, extensive career training programs, competitive health benefits, paid time off and 10 annual paid holidays*. | 7/21/2022 |
| 6437 | EAG Laboratories San Diego, CA Protein Purification Associate Bachelor's degree Exp: 1-3 years |
Eurofins Lancaster Laboratories, a nationally recognized laboratory, is searching for a Protein Purification Associate to support our Professional Scientific Services group in San Diego, CA. | 7/21/2022 |
| 6438 | Elektrofi Boston, MA Research Associate/Intern BS (Associate) or Junior/Senior (Intern) in Pharmaceutical Sciences, Chemical Engineering, Chemistry, Biology, Bioengineering, or a related field Exp: |
Elektrofi is looking for a Research Associate to join a team responsible for the development of platform formulations for Elektrofi’s proprietary microparticle production process. The Research Associate will play a key role in supporting the development of its biologics formulation platform. This individual will join an earlystage, multidisciplinary team of scientists and contribute to a variety of formulations activities in a highly collaborative environment | 7/21/2022 |
| 6439 | EMD Serono Jaffrey, NH Process Engineer Bachelor’s Degree in Engineering (e.g., Manufacturing, Industrial, Mechanical, Design) Exp: 1+ years |
At Millipore Sigma the Process Engineer will work in a dynamic environment supporting the manufacture and testing of high purity filters with a focus on quality, process control/improvements, electro-mechanical assembly, and material handling. The successful candidate will be an enthusiastic team player with high energy and strong engineering skills. | 7/21/2022 |
| 6440 | Millipore St. Louis, MO Associate Scientist Master’s Degree in Biology or Chemistry or Life Science field Exp: 1+ years |
At MilliporeSigma, as an Associate Scientist you will conduct immunoassays and Research & Development related activities within the Life Science business. This individual could be responsible for several roles focusing on new product development, product validation, troubleshooting, and Operations support for key biological reagents. This is an excellent opportunity to gain experience in groundbreaking, high sensitivity assay technologies and new product development processes in the biotechnology industry and will report to the R&D Manager. | 7/21/2022 |
| 6441 | BioReference Laboratories Elmwood Park, NJ Medical Lab Technologist (FT, 40 Hours) Bachelor of Science Degree in Medical Technology, Chemistry, Biology, or Related life Science. Exp: One or more years |
The Medical Tech performs all laboratory procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. | 7/11/2022 |
| 6442 | BioReference Laboratories Newark, NJ Medical Technician/Technologist (FT, 40 Hours) Bachelor of Science Degree in Medical Technology, Chemistry, Biology, or Related life Science. Exp: One or more years |
The Medical Tech performs all laboratory procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. | 7/11/2022 |
| 6443 | BioReference Laboratories Elmwood Park, NJ Medical Lab Technologist (FISH) Sign-On Bonus Bachelor of Science Degree in Medical Technology, Chemistry, Biology, or Related life Science. Exp: One or more years |
The Medical Tech performs all laboratory procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. | 7/11/2022 |
| 6444 | BioReference Laboratories Houston, TX Lead, Medical Technologist (FT, 40 Hours) Bachelor degree in medical technology, chemistry, biology, or related life science Exp: 1 year |
The Molecular STI Laboratory Lead Technologist will perform complex chemical, biological, testing in the detection, diagnosis, prognosis, and treatment of disease. The Lead Medical Laboratory Technologist will work collaboratively with the laboratory team to provide testing services to the clients. Additional tasks can be assigned at the discretion of the Supervisor/Manager/Director. | 7/11/2022 |
| 6445 | BioReliance [Merck KGaA] St Louis, MO Associate Scientist Master’s Degree in Biology or Chemistry or Life Science field Exp: 1+ years |
At MilliporeSigma, as an Associate Scientist you will conduct immunoassays and Research & Development related activities within the Life Science business. This individual could be responsible for several roles focusing on new product development, product validation, troubleshooting, and Operations support for key biological reagents. This is an excellent opportunity to gain experience in groundbreaking, high sensitivity assay technologies and new product development processes in the biotechnology industry and will report to the R&D Manager. | 7/11/2022 |
| 6446 | BioReliance [Merck KGaA] Rockville, MD Associate Scientist 2 Bachelor’s degree in scientific field (i.e., Biology, Chemistry, etc.) Exp: 1+ years |
We have an exciting opportunity for an Associate Scientist 2 to join our global virus production team based in Rockville, Maryland. In this role, you will perform a wide variety of routine tasks to support the virus production team in the growth of regulatory compliant virus banks, under the oversight of the Scientist. You will be responsible for performing cell culture activities, virus growths, virus titration assays and virus decontamination procedures. The ability to maintain effective working relationships with support services, scientists and all laboratory personnel are critical for success in the role. | 7/11/2022 |
| 6447 | BioReliance [Merck KGaA] Rockville, MD Associate Scientist 1 Bachelor’s Degree in scientific discipline (ie. Biology, Chemistry etc.) Exp: 0-1 years |
As an Associate Scientist 1 your activities will support assay development through commercial application of new and innovative service offerings within the biosafety testing space. You are responsible for the scientific integrity of technical work performed in the laboratory, and are required to make scientific observations, maintain detailed workbooks/documentation and ensure all documentation fulfills generally accepted professional/industry standards. Requirements also include maintaining a thorough understanding of company testing services, technical principles and applications as they apply to your position. | 7/11/2022 |
| 6448 | BioReliance [Merck KGaA] Tempe, AZ Chemist I Bachelor’s Degree in Chemistry, or similar Scientific field Exp: 1+ years |
We are currently seeking a Laboratory Technician at MilliporeSigma for the Process and Technology Group within MilliporeSigma Operations. As a part of this organization, the successful candidate will be a team member and perform laboratory tasks independently. This position will be based at the Bedford, MA campus. | 7/11/2022 |
| 6449 | BioReliance [Merck KGaA] Bedford, MA Lab Technician II Bachelor's degree in Biology, Chemistry, Biochemistry or other Science Exp: 1 year |
As an Associate Scientist/Molecular Biologist within our Next Generation Sequencing (NGS) group in our Rockville, Maryland facility, your activities will support commercial biosafety testing within the organization, specifically using NGS platforms. You are responsible for the scientific integrity of technical work performed in the laboratory, and are required to make scientific observations, maintain detailed workbooks/ documentation and ensure all documentation fulfills generally accepted professional/ industry standards. Requirements also include maintaining a thorough understanding of company testing services, technical principles and applications as they apply to your position. Your primary responsibilities will be to provide support for the day to day operation of the facility and to contribute to the timely execution of NGS service offerings for our customers. You will liaise closely with laboratory management, bioinformatics and support staff to ensure internal and external expectations are met or exceeded. You will be responsible for performing custom and routine NGS testing in accordance with all SOPs and regulations (cGMP and GLP). You will be expected to lead by example and work collaboratively to advance the application of NGS in the field of biosafety testing. | 7/11/2022 |
| 6450 | BioReliance [Merck KGaA] Rockville, MD Associate Scientist 2 Bachelor’s degree in scientific field (i.e. Biology, Chemistry, etc.) Exp: 1+ years |
As an Associate Scientist/Molecular Biologist within our Next Generation Sequencing (NGS) group in our Rockville, Maryland facility, your activities will support commercial biosafety testing within the organization, specifically using NGS platforms. You are responsible for the scientific integrity of technical work performed in the laboratory, and are required to make scientific observations, maintain detailed workbooks/ documentation and ensure all documentation fulfills generally accepted professional/ industry standards. Requirements also include maintaining a thorough understanding of company testing services, technical principles and applications as they apply to your position. Your primary responsibilities will be to provide support for the day to day operation of the facility and to contribute to the timely execution of NGS service offerings for our customers. You will liaise closely with laboratory management, bioinformatics and support staff to ensure internal and external expectations are met or exceeded. You will be responsible for performing custom and routine NGS testing in accordance with all SOPs and regulations (cGMP and GLP). You will be expected to lead by example and work collaboratively to advance the application of NGS in the field of biosafety testing. | 7/11/2022 |
| 6451 | LGC Biosearch Technologies Charleston, SC Production Chemist (40820) Bachelor of Science degree, chemistry preferred Exp: 0-2 years |
The production chemist is responsible for the manufacturing of reference standard solutions by following routine procedures and operations of laboratory equipment. This is a highly collaborative position and requires a great sense of teamwork and productivity. We are looking for individuals that can thrive in a fast-paced laboratory setting and demonstrate ability to prioritize and organize work with guidance from team leads and supervisor. Our site manufactures both catalog and custom solutions for customers requiring focused bench work, detailed record keeping and flexibility in daily tasks. | 7/11/2022 |
| 6452 | LGC Biosearch Technologies Petaluma, CA Therapeutic Production Chemist I - Night Shift (42683) Bachelor of Science in a relevant STEM field Exp: 1 or more years’ |
The Therapeutic Production Chemist I perform routine oligonucleotide manufacturing processes in the LGC Biosearch Technologies’ Petaluma Therapeutic GMP suite. Processes include: synthesis, cleavage and deprotection, purification, desalting, and lyophlization of oligonucleotides. | 7/12/2022 |
| 6453 | LGC Biosearch Technologies Petaluma, CA Therapeutic Production Chemist I - Weekend Shift (42684) BS. in a relevant STEM field Exp: 1 or more years’ |
The Therapeutic Production Chemist I perform routine oligonucleotide manufacturing processes in the LGC Biosearch Technologies’ Petaluma Therapeutic GMP suite. Processes include: synthesis, cleavage and deprotection, purification, desalting, and lyophlization of oligonucleotides. | 7/12/2022 |
| 6454 | Bio-techne Minneapolis, MN Research Associate - Quantikine Assay Development Bachelor’s degree in Chemistry, Biology or related field required Exp: up to 3 years |
The major responsibilities of this position are to develop plate-based ELISA products related to Bio-Techne's existing product lines by identifying and optimizing components to meet product performance benchmarks. Primary activities will center on assay feasibility and optimization, reagent evaluation, data analysis, literature review, stability studies and product transfer. | 7/12/2022 |
| 6455 | Bio-techne Minneapolis, MN Advanced Research Associate Master’s degree in a related field Exp: up to 2 years |
This position is responsible for participating in the development of Bio-Techne's various product lines. You will maintain knowledge of multiple products and procedures as well as draft and revise standard operating procedures in order to further the ongoing development of new and existing products to help advance Bio-Techne's evolving portfolio. | 7/12/2022 |
| 6456 | Bio-techne Newark, CA Research Associate, R&D BS in molecular biology, biochemistry, cell biology or related field Exp: 1 year |
We seek a highly motivated and creative research associate to join our R&D team. You will work within a highly dynamic group and be responsible for improving current products and developing new products based on RNAscope technology. | 7/12/2022 |
| 6457 | bioTheranostics [Hologic] San Diego, CA Entry Level Investigation Specialist B.S. in Molecular Biology, Microbiology, Chemistry, Biochemistry or Bioengineering/Biomedical Engineering Exp: 0-2 years |
Duties and Responsibilities: The incumbent may be asked to perform other function-related activities in addition to the below-mentioned responsibilities as reasonably required by business needs. Performs amplification based diagnostic assays Performs applicable internal analytical and performance testing methods used in Customer Product Support Assists with troubleshooting experimentation required for projects/investigations Trains new laboratory personnel on basic laboratory tasks. Operates basic laboratory equipment with safety mindset. General laboratory maintenance.. Assists in writing and executing protocols and reports for experimentation and qualifications as appropriate. Performs/assists with, simple to moderate investigations and prepares investigation reports/risk assessment statements as appropriate. Perform simple data analysis as required. Uses appropriate root cause analysis and lab investigation tools/process when performing investigations.Duties and Responsibilities: | 7/12/2022 |
| 6458 | Calico South San Francisco, CA Research Associate/Senior Research Associate, Proteomics BS Exp: 0-5 years |
Calico is seeking an experienced Research Associate/Senior Research Associate to join the mass spectrometry proteomics group. To succeed, you will need to be an enthusiastic team player, detail-oriented, organized and comfortable working on complex problems. We are looking for someone with detailed knowledge of proteomics and biochemistry techniques, and with demonstrated hands-on application. This is a hands-on bench position, focused on sample preparation, method development, instrument maintenance, troubleshooting and data analysis. The successful candidate will work with a large number of samples for collaborative projects, optimize and develop methods, as well as be responsible for smaller research projects. | 7/13/2022 |
| 6459 | Cambrex Durham, NC Associate Scientist II (Biopharma) Masters degree in Chemistry, Biochemistry, Molecular Biology or similar Exp: 1+ years |
As an Associate Scientist II in the biopharmaceutical team, you will work with a dynamic group of scientists supporting analytical method development, phase-appropriate validation, and testing services for viral/cellular based therapies and large molecules. | 7/13/2022 |
| 6460 | Cambrex Durham, NC Associate Scientist II (QC) MS life sciences degree Exp: 0- 1+ years |
As an Associate Scientist II in the Cambrex Quality Control team, you will be responsible for routine and non-routine cGMP testing of starting materials, drug substance, drug product, and reference standards for small molecule programs in late-phase clinical development and commercial. | 7/13/2022 |
| 6461 | Advanced Sterilization Products [Johnson&Johnson] San Diego, CA Associate Scientist I, Neuroimmunology Master's Degree in Pharmacology, Neuroscience, or Biology Exp: 1 to 3 years |
We are seeking a highly motivated Associate Scientist with in-vivo neuropharmacology experience to join our Neuroimmunology Discovery research team. The candidate should be passionate about the discovery and development of novel therapeutics for CNS disorders. Experimental work will be the core job function and as such the ideal candidate will spend close to full time at the bench generating data. It is critical that the successful candidate enjoys bench science, is scientifically curious, is self-motivated, but also a strong standout colleague, and can demonstrate a high level of efficiency. Strong interpersonal skills, the ability to interact well with peers and collaborators, and strong written and oral communication skills are vital to success in this role. To be successful in the position, the candidate must be organized, and practice good laboratory principles including detailed notebook entry of experiments.We are seeking a highly motivated Associate Scientist with in-vivo neuropharmacology experience to join our Neuroimmunology Discovery research team. The candidate should be passionate about the discovery and development of novel therapeutics for CNS disorders. | 7/13/2022 |
| 6462 | Advanced Sterilization Products [Johnson&Johnson] Spring House, PA Associate Scientist, Bioconjugates, RNA & Targeted Therapeutics M.S. degree in Chemistry, Biochemistry, Chemical/Biomedical Engineering or other related field Exp: 1 year |
In this position, the Associate Scientist will contribute to the development of various targeted therapeutics such as nucleic acid conjugates (siRNA, antisense, etc.), peptide/small molecule conjugates, or antibody conjugates. This scientist will work closely with team members to assist in the design of novel bioconjugates. S/he will primarily be responsible for the conjugation, purification, and analytical characterization of these molecules. S/he will also be responsible for routinely analyzing, interpreting, summarizing, and communicating experimental data. Additional responsibilities may include laboratory duties such as instrument and inventory maintenance. | 7/13/2022 |
| 6463 | Advanced Sterilization Products [Johnson&Johnson] Malvern, PA Associate Scientist, Large Molecule Drug Product Development M.S. degree in Engineering (Biomedical, Bioengineering, Chemical, Electrical or Mechanical) or related field Exp: 1 year |
The Associate Scientist in Large Molecule (LM) Drug Product Development (DPD) will work independently and in conjunction with development teams to support program/project needs. The candidate will also independently be accountable to lead, design, perform, and analyze studies in the development and engineering space in support of process and fill-finish activities for large molecules (e.g. monoclonal antibodies, fusion proteins, bi-specifics, gene therapies, cell therapies etc). | 7/13/2022 |
| 6464 | Advanced Sterilization Products [Johnson&Johnson] San Diego, CA Associate Scientist II MS degree in Biology, Immunology, Pharmacology, Immune-oncology or related discipline is required. Exp: 1-3 years |
The Associate Scientist will be a member of the Immunology Discovery group/Innate Immunity and function in a fast paced, highly matrixed and interactive environment. This group is focused on discovering novel therapeutics to treat various diseases including inflammatory and autoimmune diseases. | 7/13/2022 |
| 6465 | Advanced Sterilization Products [Johnson&Johnson] La Jolla, CA Associate Scientist, Discovery Chemistry (Multiple Openings) - La Jolla, CA Master’s Degree in synthetic organic or medicinal chemistry, or to be completed within 6 months, is required Exp: 1+ years |
We are seeking an experienced Bachelor’s- or Master’s-level medicinal chemist with excellent organic synthesis expertise to advance small molecule drug discovery programs toward the clinic. In this laboratory-based position, the successful candidate will partner with both internal and external medicinal chemistry teams to generate innovative solutions to synthetic and medicinal chemistry challenges within the context of small molecule drug discovery projects. They will maintain close interactions with computer assisted design scientists and biologists. Strong communication skills and the ability to thrive in a team and goal-driven environment are key attributes. This individual must also excel in communication and have strong interpersonal skills necessary to influence in a collaborative multidisciplinary environment.We are seeking an experienced Bachelor’s- or Master’s-level medicinal chemist with excellent organic synthesis expertise to advance small molecule drug discovery programs toward the clinic. In this laboratory-based position, the successful candidate will partner with both internal and external medicinal chemistry teams to generate innovative solutions to synthetic and medicinal chemistry challenges within the context of small molecule drug discovery projects. They will maintain close interactions with computer assisted design scientists and biologists. Strong communication skills and the ability to thrive in a team and goal-driven environment are key attributes. | 7/13/2022 |
| 6466 | Caris Life Sciences Tempe, AZ Research Associate - IV Research Associate - IV Bachelor’s or Master’s degree in a science field required. Exp: BS: 0-6 years; MS: 0-4 years |
Research Associates (RAs) are responsible for performing lab experiments utilizing various techniques that include, but are not limited to, Tissue (Cell) Culture, Cell Growth and Viability Assays, Immunohistochemistry (IHC), Immunocytochemistry (ICC), Cytotoxicity Assays, Gel Electrophoresis, SDS-PAGE, Western Blot, ELISA, Protein Extraction and Purification, in vivo and in vitro protein-protein crosslinking, Bioconjugation, Protein Enzymatic Digestion, Sample Preparation for HPLC and Mass Spectrometry. Furthermore, RAs are responsible for equipment maintenance, laboratory inventory, sample tracking, ordering supplies, receiving packages, and training other Research Associates. This position works under the direction of an associate research scientist, research scientist, senior research scientist, director of R&D or VP of R&D and follows standard laboratory procedures and policies. | 7/13/2022 |
| 6467 | Caris Life Sciences Phoenix, AZ Research Associate I Research Associate I Bachelor’s or Master’s degree in a science field required. Exp: 1 year |
Research Associate (RA) is responsible for performing blood processing as a member of the Biorepository. Furthermore, RAs are responsible for equipment maintenance, laboratory inventory, sample tracking, ordering supplies, receiving packages, and training other Research Associates. This position works under the direction of the Biorepository Manager and follows standard laboratory procedures and policies. | 7/13/2022 |
| 6468 | Caris Life Sciences Tempe, AZ Research Associate IV Bachelor’s or Master’s degree in a science related field is required. Exp: 0-6 years |
The successful candidate will be responsible for performing various techniques in the R&D lab. | 7/13/2022 |
| 6469 | Catalent Rockville/Gaithersburg, MD Associate Scientist I - Process Development Degree in Biology, Life Science or Chemical Engineering field Exp: B.S. with < 1 year of experience |
Catalent Cell & Gene Therapy is looking to recruit a Associate Scientist I, PD to join our growing team in Rockville/Gaithersburg, MD. The Associate Scientist I, PD is actively engaged in downstream and midstream process and product development within a dynamic project team. Displays technical knowledge, initiative and scientific commitment, and makes scientific and technical contributions within the plasmid and AAV downstream purification groups. Participate in the development and implementation of purification processes for multiple projects entering the Catalent Cell and Gene Therapy pipeline. Knowledge/expertise should be practical and focused on lab-related activities. | 7/13/2022 |
| 6470 | Catalent Morrisville, NC Associate Scientist Master’s degree Exp: 0 years |
Under general supervision, performs work that is varied and that may be somewhat difficult in character, but usually involves limited responsibility. Some evaluation, originality or ingenuity is required. Follows established protocols and work plans. May be assisted by laboratory technicians / assistants. | 7/13/2022 |
| 6471 | Catalent Bloomington, IN Associate Scientist Quality Control - Monday to Friday - 11:00P - 7:30A Bachelor’s degree OR Master’s degree in science field Exp: BS: 0-3 years; MS: 0-2 years |
Catalent is seeking an Associate Quality Control Scientist to join our growing team in Bloomington, Indiana. As an Associate Quality Control Scientist, your primary duty will be to provide quality control environmental monitoring, critical utility systems, in-process, finished products, stability, cleaning process, and analytical method validation testing according to SOPs, cGMPs and regulatory guidelines. This is a full time salaried position. The position is Mon-Fri 11:00pm to 7:30am. Catalent is seeking an Associate Quality Control Scientist to join our growing team in Bloomington, Indiana. | 7/13/2022 |
| 6472 | Catalent Bloomington, IN Associate Scientist - QC-M-F 8-5 Bachelor’s degree OR Master’s degree in science field Exp: BS: 0-3 years; MS: 0-2 years |
A quality control (QC) scientist’s primary duty is to provide quality control, in-process, finished products, stability, cleaning process, and analytical method validation testing according to SOPs, cGMPs and regulatory guidelines. Responsibilities include performing and reviewing testing during phases of production, providing technical peer review of testing data, writing/revising technical documents including laboratory procedures, protocols and technical reports, independently utilizing microbiological or analytical instrumentation such as HPLC, GC, UV, ICP-MS, FTIR, TOC, CE, ICE, Karl Fisher, , Plate Reader, performing testing using methodologies such as SDS-PAGE, , IEF, ELISA, PCR, and recognizing atypical/out of specification (OOS) results and perform investigation to determine root cause and implement corrective and preventive actions. | 7/13/2022 |
| 6473 | Catalent Madison, WI Associate Scientist - Process Development, Downstream Bachelor's degree in a STEM discipline Exp: 1-3 years |
The Downstream Process Development team is responsible for the development and implementation of downstream processing methodologies and analytical procedures that can be easily transferred to the cGMP Manufacturing Team. The process characterization function within the Downstream Process Development group will be responsible for the characterization of previously developed or transferred processes heading towards commercial manufacturing. This is a permanent, full time position. It is an hourly role. The shift is Monday-Friday 8a-5p. | 7/13/2022 |
| 6474 | Catalent Madison, WI Associate Scientist, Cell Line Development Bachelors in STEM discipline Exp: 1-3 years |
Monday – Friday, 8:00am – 5:00pm ( weekend work on a rotating basis when needed). The Cell Line Development team is responsible for using the patented GPEx® suite of technologies to create high performance stable cell lines using a non-replicative retrovector system and transfection technologies. This system can be used with any mammalian cell line and many eukaryotic cell lines. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee. The Associate Scientist, Cell Line Development, will accurately, timely, and safely perform a variety of laboratory procedures and experimental methods in Cell Line Development that support external client projects and internal technology development work. The Associate Scientist, Cell Line Development will involve performing scientific work involving the creation of cell lines, the creation, production, and purification of retroviruses, and the creation of cell banks, cell culture expansion and production, and cell culture analytical methods | 7/13/2022 |
| 6475 | Cellares South San Francisco, CA Research Associate, Analytical Development (I,II,III) MS/BS in Biological science or related scientific discipline Exp: 0-4 years |
We are seeking an innovative and highly motivated Research Associate in Analytical Development who will contribute significantly to the development of our advanced cell therapy manufacturing platform. The primary focus of this position will be contributing to method development, optimization, and qualification of various analytical methods and providing analytical service support. This is a multidisciplinary role & this individual will interface across many parts of the company (with scientists, researchers, and engineers) to develop the best solutions possible. The successful candidate will be well versed in analytical development. | 7/14/2022 |
| 6476 | Cellectis New York, NY Research Associate I, Gene Editing BS/MS or higher in life science or related discipline. Exp: 1+ years |
We are seeking a highly creative and motivated individual to join us in developing the next generation of cell therapies. The successful applicant will be part of the New York site Innovation team. The candidate will, as part of the team, develop next generation gene and cell engineering approaches using genome editing molecular tools. As part of the Innovation team, the candidate will contribute to the ongoing efforts toward the development of differentiated therapeutic approaches using our gene editing technologies. Candidates should be highly self-motivated with the ability to excel in a fast-moving, goal-oriented environment. | 7/14/2022 |
| 6477 | Cenetron Diagnostics [Versiti] Wauwatosa, WI Research Technologist - Kastrup Bachelors degree from an accredited college or university in biology, chemistry, scientific discipline Exp: One to three years |
Under the direction of the Principal Investigator, performs laboratory assays and complex experiments to elucidate novel research questions. | 7/14/2022 |
| 6478 | Cenetron Diagnostics [Versiti] Milwaukee, WI Laboratory Technologist - Research Bachelor’s degree from an accredited college or university in biology, chemistry, molecular biology, immunology, clinical laboratory science, medical Exp: one year |
Under supervision by department leadership, this position will support the Hemolysin Assay for organ transplants: Building a donor specific antibody (DSA) model from blood group antigen array data (recognition of RBC glycoproteins) The primary objective is to compare the HLA and blood typing of individuals with their glycan profile using glycan related measures to predict risk. Using glycan-related measures including DNA/RNA analyses, microarrays and antibody testing, a glycan profile can be established and compared to HLA and blood typing results. Small study already conducted, but looking to expand sample size. | 7/14/2022 |
| 6479 | Cenetron Diagnostics [Versiti] Wauwatosa, WI Research Technologist I - Branchford Bachelors degree from an accredited college or university in biology, chemistry, scientific discipline Exp: One to three years |
Under the direction of the Principal Investigator, performs laboratory assays and complex experiments to elucidate novel research questions. | 7/14/2022 |
| 6480 | Cenetron Diagnostics [Versiti] Milwaukee, WI Associate Laboratory Technologist - PNIL Lab- SIGN ON $3500 Bachelor’s degree from an accredited college or university in biology, chemistry, molecular biology, immunology, clinical laboratory science, medical Exp: Entry-Level |
Under direct supervision by department leadership, performs CLIA regulated and clinical contract research testing. Interacts at a basic level with customers, providing a high level of customer service to resolve customer concerns about sample acceptability and results. Supports preparation of laboratory reagents and routine maintenance of laboratory equipment . | 7/14/2022 |
| 6481 | ANI Pharmaceuticals Baudette, MN Analytical Development Chemist Analytical Development Chemist Analytical Development Chemist Bachelors degree in chemistry, biochemistry, microbiology or closely related field or major. Exp: 1-3 years |
This position is responsible for independently performing testing in a pharmaceutical analytical development laboratory. All work will be conducted in accordance with standard operating procedures and test methods. This is a professional position that requires 2-5 years previous experience working in a laboratory performing chormatographic analysis and dissolution testing. | 7/4/2022 |
| 6482 | Ansh Labs Webster, TX SCIENTIST (Monoclonal Lab) Master’s degree in Biology or related area Exp: one or more years |
As a key member of the monoclonal antibody department, this individual will provide critical cell culture, protein engineering, and molecular biology expertise enabling the discovery, design and production of monoclonal antibodies and antigens. | 7/4/2022 |
| 6483 | Ansh Labs Webster, TX SCIENTIST (R&D) Master’s degree in Biological/Chemical Sciences/Biotechnology or related area Exp: 1 year |
As a key member of the R&D department, this individual will provide critical scientific skills to assists in the development and scale up of immunodiagnostic product on various platforms (microtiter based ELISA, magnetic particle based immunoassays, lateral flow assays and micro fludics based immunoassays. | 7/4/2022 |