6648 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 | CryoLife Kennesaw, GA DQA Analyst BS in Biological Sciences Exp: 0+ Years |
Responsibilities: Ensure that all donors accepted and processed at CryoLife are properly identified, controlled, and meet all required quality specifications and regulatory standards prior to release for distribution. Provide support to Account Managers and facilitate obtaining donor chart information to accurately complete donor chart reviews. Organize donor chart information and all charting follow-up to meet required chart review targets and workflow. Maintain accurate pending chart information lists and pending additional information. | 2/19/2021 |
| 2 | Cook Medical Bloomington, IN Change Specialist BS in Relevant Discipline Exp: 0+ Years |
Responsible for facilitating and monitoring the CMMS Document Management and Change Control process from change proposal through release of documentation. Responsible for facilitating training assignments for CMMS documentation and for serving as point of intake for Internal Customer Feedback. | 2/12/2021 |
| 3 | Cerba Research New Hyde Park, NY Associate Scientist - Flow Cytrometry MS in Biology or Related Exp: 1-2 Years |
The Associate Scientist is a key scientific position to support the flow cytometry division in data analysis and data reporting to the clients. The Associate Scientist is critical in identifying data abnormalities and troubleshooting with the help of flow cytometry scientists. The Associate Scientist will have a critical role in reporting quality data to clients. | 2/5/2021 |
| 4 | CogMedix West Boylston, MA Electrical Engineer I BS in Electrical Engineering Exp: 0-5 Years |
As a member of the engineering services team, the Electrical Engineer I will solve complex problems and participate in the specification, design, prototyping and testing of a diverse range of tooling, fixtures, design for manufacturability projects, and other customer product design needs. Under the direction of the Electrical Engineering Manager, the engineer in this role will be performing design tasks of a complex technical nature requiring investigation of new technologies, and applying engineering design principles and practices. | 2/5/2021 |
| 5 | Phillips San Diego , CA IVUS R&D Engineer BS in Biomedical, Mechanical, Plastics, or Electrical Engineering, or Materials Science Exp: 1+ Years |
Provides technical expertise to the design and development of new invasive and noninvasive 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 and verification studies of the design and design related processes/test methods to demonstrate intended function. 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. | 1/29/2021 |
| 6 | Phillips Monroeville, PA Mechanical Engineer - Oxygenation & Ventilation BS/MS in Mechanical, Biomedical, Plastics, or Related Engineering Exp: 0+ Years |
In this role, you have the opportunity to participate in the design, implementation, test, and documentation efforts necessary to support the development of mechanical components for use in Oxygenation and Ventilation medical devices. This role is for Research and pre-development. The candidate will work on tasks and assign tasks necessary to meet project goals for products being developed for Sleep and Respiratory Care. | 1/29/2021 |
| 7 | Phillips San Diego , CA Digital Electrical Engineer BS/MS in Electrical Engineering Exp: 0+ Years |
As an Electrical Engineer, you will be responsible contributing to the design and development of intravascular imaging and functional measurement devices. You will utilize your knowledge and expertise in circuit design and testing to create market-leading products. This position within IGT-D R&D collaborates closely with other R&D functions (mechanical, systems, etc.), Marketing, Clinical Affairs, Procurement, and Quality Regulatory. | 1/29/2021 |
| 8 | Novartis Millburn, NJ Production Technician BS in Engineering or Scientific Discipline Exp: 0+ Years |
The Production Technician plays an active role in daily production of Lutathera as well as setup and preparation of instruments and equipment. Due to the nature of the process (radioactive) this role requires basic proficiency, ownership of the process and understanding of radiation safety standards. | 1/22/2021 |
| 9 | Novartis Cambridge, MA Computational Biologist, Oncology Data Science MS in Computational Biology, Bioinformatics, Data Science, or Related Exp: 1+ Years |
Responsibilities: Working closely with interdisciplinary teams of wet lab and dry lab collaborators to analyze and interpret high-dimensional biological data (e.g., bulk RNAseq, single-cell RNAseq, CRISPR screens, proteomics) to inform critical project decisions. Implementing and developing state-of-the-art computational methods and data mining strategies to address key challenges in oncology drug discovery. Identifying novel drug targets on cancer cells, immune cells, and/or other cell types in the tumor microenvironment. Deepening our understanding of drug resistance and strategies to overcome it. Formulating testable biological hypotheses and collaborating in the design of rigorous preclinical experiments. Driving forward multi-disciplinary collaborations and projects, and establishing them as needed. | 1/22/2021 |
| 10 | Novartis Cambridge, MA Vivarium Operations Technician BS in Relevant Discipline Exp: 0+ Years |
Vivarium Operations (VO), as a function of Comparative Medicine (CM), provides high quality animal care to laboratory animals enrolled in studies within 14 disease area teams within NIBR. VO is looking for the ideal candidate to fill an entry level vivarium operations technical position responsible for maintaining the health and welfare of laboratory animals and supporting research by doing daily health and checks and husbandry, organizing facility data and records, and helping with all daily facility needs. This position will closely collaborate with the CM organization and NIBR disease area teams within our multi-building, multi-discipline, multi-species research program, focusing on the zebrafish with some rodent work as well. | 1/22/2021 |
| 11 | Novartis Carlsbad, CA Associate Scientist, High Dimensional Flow Cytometry MS in Scientific Discipline Exp: 0-4 Years |
As an Associate Scientist at Navigate, you will help to design, create, execute, and troubleshoot Flow cytometry based procedures and assays. You will be expected to exhibit moderate to high level of independence while working on multiple projects including contributing to the launch of new platforms/assays. Candidates must demonstrate critical thinking, initiative and effective stakeholder management in the execution of their projects. | 1/22/2021 |
| 12 | Novartis Cambridge, MA Research Scientist - Sickle Cell Disease, Hematology MS in Biology, Chemistry, or Pharmacology Exp: 0+ Years |
Responsibilities: Will assume a crucial role in the development of novel therapeutic concepts and will contribute at all stages of a project, from inception, early project validation, optimization, candidate selection and through to early clinical development of novel medicines for patients with sickle cell disease. Will work collaboratively with other specialists to develop project strategy, identify key drug discovery issues, propose and implement creative solutions, execute and guide teams to success and decision points. He/she will conduct early research to develop in vivo targeted gene delivery strategies for Sickle Cell Disease. | 1/22/2021 |
| 13 | Novartis Cambridge, MA Scientific Associate I, Veterinary Medicine BS in Scientific Discipline Exp: 0+ Years |
VM is looking for the ideal candidate to fill an entry level veterinary technical position responsible for maintaining the health and welfare of laboratory animals and supporting research by triaging emergencies, treating common clinical conditions in laboratory animals, and recognizing study-related clinical trends. This position will closely collaborate with the CM organization and NIBR disease area teams within our multi-building, multi-discipline, multi-species research program. | 1/22/2021 |
| 14 | Novartis Carlsbad, CA Associate Clinical Laboratory Scientist BS in Scientific Discipline Exp: 0+ Years |
Responsibilities: Works in a GMP/GCP/GLP/CLIA regulated environment and is responsible for following all applicable regulations. Assist in activities related to validation of new laboratory tests, new instrumentation, and new laboratory software. Perform all clinical specimen testing (pre-analytical/analytical procedures) as assigned under supervision. Use LIMS to perform sample management, testing worklists, enter test results and QC data. Adheres to established turn-around-times while maintaining highest quality of test results. | 1/22/2021 |
| 15 | Biogen Research Triangle Park, NC Engineer I, Process BS/MS in Relevant Scientific Discipline Exp: 0-2 Years |
The position provides responsible engineering support for GMP (Good Manufacturing Practice) equipment in a Cell Culture and/or Purification area including bioreactor, perfusion, chromatography, centrifugation, UF/DF, solution preparation and filtration operations. Designs, specifies, installs, and commissions new equipment and provides engineering technical support and troubleshooting for cell culture or purification processing equipment including associated automation. Engagement and support of process tech transfers is required to ensure manufacturing equipment meets process requirements. Investigates process or equipment failures and implements changes to avoid future occurrences. Provides support for new equipment evaluations and process improvement studies. Investigates equipment failures and implements changes to avoid future occurrences. Provides support for site and global regulatory inspections, as needed. | 1/13/2021 |
| 16 | Biogen Cambridge, MA Bioinformatics Engineer BS/MS in Computational Biology, Bioinformatics, Bioengineering, or Computer Science Exp: 1-3 Years |
This role will fall under the Genome Technology and Computational Sciences group which provides scientists with cutting-edge computational informatics and analytics tools and services in support of research and early development. The team has the technical depth, agility and great motivation to solve scientifically demanding problems. The Bioinformatics Engineer will be involved in the development of bioinformatics pipelines, R Shiny applications, and visualization tools. This position will also be responsible for developing bioinformatics tools and implementation of laboratory information systems. | 1/13/2021 |
| 17 | Biogen Cambridge, MA Associate Scientist II, Gene Therapy - Cell Line Technology BS in Biology Exp: 0-2 Years |
The candidate will capitalize on their skills in molecular biology to engineer stable cell lines and viral vectors to support development of gene therapy manufacturing platforms. A background in cell biology, bioengineering, or microbiology is highly valued. Experience with molecular cloning, viral vector engineering, and high-throughput mammalian cell culture is preferred. The successful candidate will work efficiently with team members and independently to plan, conduct, analyze, and document experiments to drive innovation in a cutting-edge modality. | 1/13/2021 |
| 18 | Biogen Cambridge, MA Associate Scientist III, Protein Drug Product Development MS in Chemical Engineering, Biochemical Engineering, Biotechnology, or Related Exp: 0-2 Years |
As a member in Biogen’s Protein Drug Product Development team, the candidate will be primarily responsible for supporting formulation, process, and container development of parenteral drug products. This includes an emphasis on process and formulation development along with associated analytics. The ability to work independently, collaboratively in an innovative, agile manner are key attributes for the successful candidate. The individual is expected to present findings and/or results internally within the department and to external stakeholders, and author study reports. The role will involve developing, assessing, and implementing new technologies along with developing platforms, aligned with the department’s long-range technology development plans | 1/13/2021 |
| 19 | Biogen Cambridge, MA Production Operation Specialist II, External Manufacturing BS in Quality, Engineering, Supply Chain, or Related Exp: 1-2 Years |
The Production Operations Specialist maintains day-to-day Oracle production activities and works closely with the CMO Virtual Plant Teams to maintain systems and production timelines. Responsibilities: Execute external production-related transactions in Oracle in a timely and accurate manner. Generate purchase orders and perform invoice reconciliation. Ensure production readiness (e.g. authorizations-to-manufacture). Create and update production batches in alignment with production planning (updated due dates, planned dates, and actual dates for production and release steps). Align proactively with CMO Virtual Plant Teams regarding ongoing production, priority batches and production challenges. Leads or supports continuous improvement projects, metrics reporting, process documentation and training. | 1/13/2021 |
| 20 | Biogen Cambridge, MA Engineer II, Device Design and Process Development MS in Engineering Exp: 0-2 Years |
Biogen is seeking a qualified candidate for the role of device design and process development Engineer II in the Medical Devices & Packaging Department. The position will lead the design and process development of patient-centric, safe, reliable, and innovative devices. Beginning with continuous research of cutting-edge technology to develop delivery systems integrated with the pipeline. Effectively and efficiently bring optimized products to market through rigorous science and engineering by leveraging external partnerships in collaboration with internal Human Factors, Packaging, Manufacturing Science, Engineering, Quality and Regulatory Affairs etc. | 1/13/2021 |
| 21 | Biogen Cambridge, MA Associate Scientist II, Cell Culture Development, Gene Therapy BS/MS in Bioengineering, Biochemical Engineering, Biochemistry, or Related Exp: 0-2 Years |
Biogen is presently looking to fill an Associate Scientist II position within its Gene Therapy Process Development department. Candidate must be motivated and innovative with exceptional analytical and communication skills. Responsibilities: Assist with experimental design and execute laboratory experiments with minimal guidance. Perform independent data recording and analysis. Troubleshoot in-lab activities. Work with small- and large-scale operations depending on need. Document development work in concise reports and provide project updates in written and oral presentations. Support maintenance tasks and new technology evaluations for laboratory instrumentation; interact with outside vendors/suppliers. | 1/13/2021 |
| 22 | BioRad Woodinville, WA Production Chemist I BS in Physical Sciences Exp: 0+ Years |
Manufacturing activities for BioPlex 2200 to support commercialization and development activities. Areas of responsibility could include bead coupling, conjugation, calibrator and control manufacturing, or other component manufacturing. | 1/13/2021 |
| 23 | August Bioservices Nashville, TN Lab Research Technician, Protein Science BS in Biology, Chemistry, Biochemistry, or Related Exp: 1-2 Years |
The Lab Research Technician will work within a team of highly motivated laboratory staff and scientists. This role will have a significant impact on the team’s progress through direct involvement in specific projects and support the daily operations in the Research Services lab. The chief role of this employee is to assist senior laboratory personnel with administrative lab duties and with protein expression and purification activities. The job involves performing sanitation and sterilization of labware, assisting with inventory management & equipment maintenance. The successful candidate should also understand and be able to apply basic molecular biology and protein chemistry techniques. | 12/29/2020 |
| 24 | August Bioservices Nashville, TN Microbiologist BS in Biology or Related Exp: 0-3 Years |
August Bioservices is seeking a Microbiologist to join their growing Analytical Development team. This is an entry-level role and recent grads are encouraged to apply. Reporting to the Manager, Analytical Development the Microbiologist will be responsible for performing environmental monitoring sampling of ISO class environments and assisting with preparation, characterization, and identification of environmental isolates. The Microbiologist will perform raw material and drug product method development and cGMP testing. | 12/29/2020 |
| 25 | Auris Robotics & Digital Solutions Santa Clara, CA Mechanical Engineer BS in Mechanical Engineering or Related Exp: 1+ Years |
Responsibilities: As a member of the Surgical Robotics Instruments and Accessories Integration Team, you will contribute to the development and support of robotic instrumentation for a surgical robotic platform. Progress development of novel instrumentation spanning from feasibility through to product launch. Solve and perform rout cause analysis of failures seen when instrumentation are used with the Robotics Platform. Build multi-functional relationships with a multitude of different department representatives. Design and create prototypes using in-house rapid prototyping capabilities. Provide hands-on, troubleshooting, process and manufacturing support as well as designing, implementing, integrating and testing solutions in a fast pace environment with a quick development cycle. Create design solutions utilizing engineering methods with good documentation processes, releasing design documentation through an ECO process in accordance with the company design control process. | 12/29/2020 |
| 26 | Avantor West Henrietta, NY Chemistry Technician BS in Biology, Earth Science, Environmental Science, or Related Exp: 0+ Years |
Receive, evaluate, and process living or non-living raw material into finished product. Perform quality control check on final product, adhering to departmental standards. Performance will be assessed based upon the quality of the finished product and the efficiency of its manufacture. Answer customer service questions and provide technical support. Tasks may include some warehousing, inventory control, and other indirect tasks. | 12/31/2020 |
| 27 | Avantor Eatontown , NJ QA Inspector BS in Relevant Discipline Exp: 0+ Years |
Ensures customer and regulatory requirements have been met by inspecting incoming raw materials and review of documentation. Ensures compliance with all applicable standards and regulations (e.g., ISO 9001, ISO 13485, 21 CFR 820, 21 CFR 11, Good Manufacturing Practices (cGMPs), and Good Documentation Practices (GDPs). | 12/31/2020 |
| 28 | Avantor Phillipsburg , NJ Chemical Technician BS in Science or Related Discipline Exp: 0+ Years |
The Chemical Technician completes procedures associated with manufacture of pilot scale batches of chemical according to established or developmental procedures. Handles raw materials (including 55 gal. drums) and process waste associated with this manufacturing. Operates various unit operations and pilot lab systems. This is a bargaining unit shift position. | 12/31/2020 |
| 29 | Avantor Paris, KY Technician QC Lab BS in Chemistry, Biology, or Microbiology Exp: 1-3 Years |
Responsibilities: Conducts routine and non-routine chemistry and microbiological analysis of raw materials, in-process formulations and final products to established specifications. Utilizes and operates laboratory equipment and instruments according to laboratory work instruction or laboratory procedures such as pH, conductivity, UV, KF, FTIR and titrations. Ability to understand and follow Quality Control test methods or compendia methods (USP, EP, BP, JP or ACS) and EXCIPACT standard. Calculates and generates data for compliance to specifications and reports results. Performs technical review of lab data forms such as water, environmental monitoring and direct measure analysis. Calibrates and maintains lab equipment. Enters final results and raw data for tested materials or products in LIMS (Laboratory Information Management System) as needed. | 12/31/2020 |
| 30 | Avantor Rensselear, NY Lab Support Specialist BS in Relevant Discipline Exp: 0+ Years |
Perform laboratory tests, experiments, and analyses. Closely follows standard procedures in laboratory testing, evaluating various routine assay, and in performing tasks related to stability studies, sterility testing, investigating product complaints, and evaluating new and existing product. Assists in operating manufacturing equipment and systems in a lab environment along with purification product-related operations. Follow blueprints, guidelines, and/or diagrams to ensure product specifications are met. Assist in the assembly or sub-assembly of life science products and devices. Adhere to Good Manufacturing Practices (GMPs) and Standard Operating Procedures (SOPs). | 12/31/2020 |
| 31 | AvoMeen Ann Arbor, MI Analytical Chamist/Scientist BS/MS in Chemistry Exp: 0-5+ Years |
Responsibilities: Learn techniques spanning across the entire spectrum of analytical chemistry from wet chemistry to HPLC, NMR, Mass Spectrometry, FTIR, GC and GC-MS. Perform testing using a variety of technologies including HPLC, LC-MS, GC, GC/MS, Microscopy, FTIR and UV. Execute projects in support of client needs including product deformulation and product development, failure analysis and problem solving, impurity identification, extractable and leachable studies, and structural characterization. Follow all safety requirements including wearing appropriate personal protective equipment. Generate supporting laboratory documentation. Ensure compliance with government rules and regulations (FDA, cGMP, DEA, ICH, OSHA, etc.). Implement new equipment and processes independently, capable of conducting appropriate qualification and validation activities. | 12/31/2020 |
| 32 | Bausch & Lomb Greenville, SC Sterilizer Operator BS in Relevant Discipline Exp: 0+ Years |
Load/unload totes and place dosimeters on product. Transfer pre-sterilized product into the APA. Unload trucks of non-sterile components from vendors and prepare them for processing while ensuring separation of sterile and non-sterile components. Place and read dosimeters using a digital micrometer and spectrophotometer. Operate Irradiator Console to set timer settings and clear faults/settings. PC Data entry to include dosimetry information and basic inventory receipt transactions in ERP Lx. Analyze and correct irradiator faults by interpreting program logic controller display indicators and repositioning switches, totes and sensors on the source pass as well as the entry and exit conveyors. Operate industrial irradiator and will load and unload components to ensure proper sterilization during irradiation operations. | 12/31/2020 |
| 33 | Bausch & Lomb Greenville, SC Sterile Prep Operator BS in Relevant Discipline Exp: 0+ Years |
Maintain the APA in accordance with SOPs and within environmental monitoring limits by cleaning and sanitizing all equipment and rooms inside and adjacent to the APA. Document all cleaning and sanitization processes according to SOPs. Perform CIP and SIP processes for Fill Room Equipment. Install and test filters as required. Maintain the APA in orderly conditions by removing culls, performing regular inspections of the equipment and environment and using Aseptic Technique. Prepare and stock process materials for use inside the APA. | 12/31/2020 |
| 34 | Bausch & Lomb Petaluma, CA Chemist III BS in Chemistry or Related, MS Preferred Exp: 0+ Years |
Directs and provides analytical support for research, development, and manufacturing activities. Provides high level troubleshooting and analytical method development and method validation per pharmaceutical guidelines. Ensures that laboratory work is in compliance with regulations. In-depth understanding of cGMPs, CFRs and ICH Guidances for pharmaceutical development. Prepares complex technical experimental designs and reports. Experienced in HPLC, wet chemistry analysis, and laboratory data systems. Safety minded in operation. | 12/31/2020 |
| 35 | Baxter Round Lake , IL Senior Engineer - Reliability MS in Engineering Exp: 1+ Years |
Support plant equipment reliability through the implementation of projects improving or optimizing the computerized maintenance management systems (CMMS) and reliability systems by increasing data quality, improving reporting methods / analysis tools, and developing related policies / processes. Lead and participate in Kaizen and Lean Maintenance events. Lead engineering projects such as equipment or process improvements through project conceptualization, project design, machine design, development of alternatives, project scheduling and control, and project installation and implementation. | 12/31/2020 |
| 36 | Baxter Bloomington, IN Process Engineer II BS in Engineering Exp: 1-3 Years |
An Engineer II is responsible for continuous improvement, floor support and troubleshooting as required on assigned filling lines and processes (both mechanical and electrical). An Engineer II will be responsible for development of requirements specifications, technical specifications, design specifications, validation protocols, and change control records. This position will work with Program Managers to facilitate new product introduction to the site (vendor relations, procurement, installation, and validation) and achieving both budget and timeline requirements. This position reports to the Manager of Engineering. | 12/31/2020 |
| 37 | Baxter Bloomington, IN Quality Lab Associate BS in Chemistry or Analytical Chemistry Exp: 0+ Years |
The Quality Lab Associate I (2nd Shift) performs entry-level laboratory testing (pH, density, volume, etc.) that requires a variety of chemical, biological, or physical analyses on products/systems in support of the company’s quality program. This role works as part of the quality unit. This position reports to a Quality Control Chemistry Supervisor. | 12/31/2020 |
| 38 | Baxter Opelika, AL Quality Lab Technician BS in Chemistry or Biological Sciences Exp: 0-2 Years |
This is a second shift position intended to perform Quality Control Testing to support the acceptance of raw materials and finished products. This position will cross-train to perform all laboratory tests to support dialyzer manufacturing. These tests will include microbiological, chemical, and performance tests. The technician may at the discretion of the QRM Manager have primary responsibility in either the Microbiology Laboratory or the Chemical Laboratory. | 12/31/2020 |
| 39 | Baxter Cleveland, MS Engineer I BS in Engineering Discipline Exp: 0-1 Year |
Responsibilities: Must perform process validation, process capability, and process control studies for assigned areas. Must drive quality/manufacturing projects utilizing Lean, problem solving, process control, and project management tools to achieve and sustain operational excellence. Must support Manufacturing, Engineering, and Quality Management departments with the development and implementation of new process/technology. Must assist in the identification and development of process improvement projects including automation and computerization. Must ensure computer systems and applications are in compliance with regulatory quality standards through validations activities. Responsible for ensuring FDA regulations are met for system upgrades/replacements. Responsible for ensuring the quality of facility systems (validation). Writing and executing protocols and test cases for validations. Coordinating testing and documentation of projects. | 12/31/2020 |
| 40 | Be Bio Cambridge, MA Research Associate - Cell Platform MS in Relevant Discipline Exp: 1+ Years |
Responsibilities: Help to establish protocols around differentiation of primary immune cells, including extensive tissue culture work (maintenance, expansion, and banking). Handling and analyzing workflows pertaining to cellular differentiation and profiling with downstream qRT-PCR, protein quantification, and other molecular readouts. Cloning of constructs to support cellular engineering efforts. Detailed record-keeping and protocol refinement as related to molecular and cellular assays. Facilitate efficient transfer of assays to CRO partners where applicable. | 12/31/2020 |
| 41 | Beckman Coulter Miami, FL Manufacturing Process Engineer BS in Engineering Exp: 0-3 Years |
Responsibilities: Facilitate Kaizen and DIVE teams to ensure accurate use of DBS tools. Identify cost-savings and quality improvement projects in assigned area(s) and move them from concept to implementation. Develops and writes SOP’s to support process changes, implementation of new processes and equipment, ensuring manufacturing documents are crafted, updated, and implemented. Provide mentorship for engineering technicians. Coordinates the launch of new product designs and enhancements to existing product designs to ensure smooth transition to full production. Confers with management, engineering, and other staff regarding manufacturing capabilities, production schedules, and other considerations to ensure smooth transition of new or enhanced product and/or processes to full production. | 12/31/2020 |
| 42 | Beckman Coulter Brea, CA Proposal Analyst II MS in Relevant Discipline Exp: 0+ Years |
You will be responsible for the development and management of error proof contract documents while maintaining high attention to detail. You will also be required to provide insight and business recommendations based on deal analysis. This role is responsible for identifying any discrepancy or potential gaps in the deal elements and focusing on continuously improving the process; recommending solutions and sharing best practices. Analyst II are responsible for reviewing redlines of contract terms and conditions in close partnership with legal, sales and direct customer interaction for timely turnaround time (TAT). The role will maintain close collaboration with other departments/stakeholders including sales, sales management, operations, marketing, legal and finance. You will need to know how to work independently as well as in a team environment. We are looking forward to partnering with you. | 12/31/2020 |
| 43 | Beckman Coulter Chaska, MN Supplier Quality Engineer II MS in Relevant Discipline Exp: 0-2 Years |
As the Supplier Quality Engineer II, you will work with cross-functional teams and ensure suppliers deliver quality product on an on-going basis, while developing supplier capabilities for future needs. This includes material specification development, supplier selection & approval, material qualification, material control and supplier development activities. You'll independently plan, coordinate, and report on material projects and supplier performance. Your sound technical ability and decision making will achieve the desired results. You'll represent Supplier Quality on new product development, manufacturing, and product improvement projects. | 12/31/2020 |
| 44 | Beckman Coulter Carlsbad, CA Senior Technician Quality Control BS in Chemistry, Biology, or Medical Terminology Exp: 1+ Years |
Responsibilities: Testing and inspecting assigned products including raw materials, bulks and final products for clinical chemistry assays, including general chemistry and specialized tests such as therapeutic drug monitoring and drugs of abuse. Weigh samples on analytical balances, prepare solutions, and process samples following defined SOPs. Use general laboratory equipment such as balances, pH meters, and spectrophotometers. Use Beckman Coulter clinical analyzers such as DxC and Immage systems. Investigate and troubleshoot problems when needed. Interface with R&D, manufacturing technical operations, quality assurance, and supply chain within the company. Perform microbiological and spectrophotometric test of clinical diagnostic reagents and finished products. Perform calibration, standardization, and maintenance of laboratory instruments and equipment. | 12/31/2020 |
| 45 | Beckman Coulter Carlsbad, CA Development Scientist II MS in Biology or Chemical Science Exp: 0-2 Years |
The Research and Development department is looking for a Development Scientist to support the manufacture of clinical chemistry reagents including design changes, failure investigations and Verification/Validation studies. In addition, this role will act as a liaison between Development and current production, facilitating the transfer process and assisting in troubleshooting activities. This individual will also work on future development project initiatives for the department as project priorities and manufacturing support allow. | 12/31/2020 |
| 46 | Beckman Coulter Minneapolis, MN Mechanical Engineer II MS in Mechanical Engineering Exp: 0-2 Years |
This position will have a focus on investigating, designing and improving mechanical systems including motion control, fluid handling, electro-mechanical system hardware, and packaging. Responsibilities: Lead reliability investigations, cost reduction efforts, and mechanical design improvements. Engage in new product concepting and development. Perform both empirical and theoretical analysis; interpret experimental data to formulate conclusions. Create and maintain detailed component level drawings that include material specifications, material coatings, tolerancing and GD&T. Develop test criteria and executing test plans. Develop project schedules, track and communicate project status, and provide leadership and ownership of project deliverables. | 12/31/2020 |
| 47 | Beckman Coulter Miami, FL Manufacturing/Process Engineer I BS in Engineering or Related Exp: 0-3 Years |
The Manufacturing Process Engineer for Beckman Coulter Diagnostics takes ownership of determining the optimal manufacturing methods and process. This includes driving continuous improvement to product cost, quality, and performance by using technical experience and judgment to tackle engineering problems. This position is part of the manufacturing engineer team and will be located in Miami, FL. Responsibilities: Facilitate Kaizen and DIVE teams to ensure accurate use of DBS tools. Identify cost-savings and quality improvement projects in assigned area(s) and move them from concept to implementation. Develops and writes SOP’s to support process changes, implementation of new processes and equipment, ensuring manufacturing documents are crafted, updated, and implemented. Provide mentorship for engineering technicians. | 12/31/2020 |
| 48 | BeiGene San Francisco, CA Document Specialist, Medical Writing BS/MS in Life Sciences Exp: 1+ Years |
The Document Specialist, Medical Writing will support/assist in the writing, editing, formatting and overall development of clinical regulatory documents that conform to domestic and/or international regulatory submission and internal document standards, while meeting project timelines. Clinical regulatory documents include, but are not limited to, study reports, clinical study protocols or amendments, investigator brochures, regulatory briefing documents, and clinical sections of INDs, NDAs, BLAs, MAAs and other regulatory submission documents. | 12/31/2020 |
| 49 | BeiGene San Mateo/Remote, CA Project Coordinator (Contract) BS in Project Management, Life Sciences or Related Exp: 0-2 Years |
The Project Coordinator will collaborate closely with program managers to provide support for a range of project planning/management activities. This role will work closely with various members of the project team to develop timelines, create schedules, and oversee progress to make sure goals are met on time. Responsibilities: Provide support and assistance to program managers in completion of all required tasks to meet departmental and project goals. Responsible for the maintenance of plans and timelines within MS Project, and communicating project status in designated platforms. Assist with developing program management dashboards, reports and presentations. Generate and publish weekly project and program reports; incorporate process improvements and innovation in developing new reports. Assist in coordinating project/program meetings; collecting agenda and action items and creating meeting minutes. Be an active participant in Project Management staff meetings. | 12/31/2020 |
| 50 | Berg Framingham, MA Research Associate I - Functional Lipidomics BS/MS in Analytical Chemistry, Biochemistry, or Related Exp: 0+ Years |
The Research Associate I will be responsible for biomarker discovery/validation in multiple disease areas, including neurodegenerative diseases, diabetes, obesity, and cancer, using state-of-the-art quantitative lipidomics platforms. Responsibilities: Familiarity with Mass Spectrometry. Hands-on experience with mass spec quantitative and qualitative data analysis including spectral interpretation is a plus. Excellent communication and interpersonal skills combined with a superior and proven track record of technical and organizational skills. Must be able to work in a team-oriented environment and demonstrate attention to detail and record-keeping. | 12/31/2020 |
| 51 | Berg Framingham, MA Data Research Associate II - Neurology Scientist BS/MS in Biology, Biochemistry, Neuroscience, or Related Exp: 1-2 Years |
The RA II will characterize novel therapeutic targets for neurodegenerative diseases and assists in the development of potency assays and phenotypic screens in vitro. Responsibilities: Assist in the characterization of novel diagnostic biomarkers and therapeutic targets for Alzheimer’s and Parkinson’s disease using standard molecular biology techniques. Identification, development, and implementation of cutting-edge methods for characterizing lead biomarker and therapeutic candidates. Contribution to assay development and small molecule screens. Maintain and differentiate several cell lines to support the research efforts of the Neurology department. Report research findings in an organized, clear and timely manner. | 12/31/2020 |
| 52 | Berkeley Lights New York City, NY Applications Development Engineer MS in Chemical, Mechanical, or Electrical Engineering, or Related Exp: 0-3 Years |
This research and development role resides at the interface of several teams within the organization, including the software and hardware engineering teams, the chip design and reagents team, and product marketing. In this position, you will have the opportunity to create new capabilities on the Berkeley Lights platform, taking products from early conception through product launch. Responsibilities: Work closely with collaborators and customers to design solutions leveraging Berkeley Lights’ platforms with a focus on Cell Therapy and T cell immunology applications. Contribute to shaping and guiding the design, development and productization of T cell functional assays uniquely enabled by Berkeley Lights’ platforms. End-to-end workflow development involving precious sample handling, microfluidic-based workflow development, and workflow automation. Validation and verification of complex life science instrumentation. | 12/31/2020 |
| 53 | Berkeley Lights Emeryville, CA Associate Development Engineer BS/MS in Chemical, Mechanical, or Electrical Engineering, or Related Exp: 0-3 Years |
This research and development role resides at the interface of several teams across Berkeley Lights, including the software and hardware engineering teams, the chip design and reagents team, and product marketing. In this position, you will have the opportunity to create new capabilities on the Berkeley Lights Platform, taking products from early conception through product launch. Responsibilities: End-to-end workflow development involving precious sample handling, microfluidic-based workflow development, and workflow automation. Validation and verification of complex life science instrumentation. Contribution to the invention of core intellectual property (from conception through validation), white papers, and external publications. This research and development role resides at the interface of several teams across Berkeley Lights, including the software and hardware engineering teams, the chip design and reagents team, and product marketing. In this position, you will have the opportunity to create new capabilities on the Berkeley Lights Platform, taking products from early conception through product launch. Responsibilities: End-to-end workflow development involving precious sample handling, microfluidic-based workflow development, and workflow automation. Validation and verification of complex life science instrumentation. Contribution to the invention of core intellectual property (from conception through validation), white papers, and external publications. | 12/31/2020 |
| 54 | Berkeley Lights Emeryville, CA Development Engineer MS in Chemical, Mechanical, or Electrical Engineering, or Related Exp: 0-3 Years |
This research and development role resides at the interface of several teams within the organization, including the Software and Hardware Engineering teams, the Chip Design and Reagents team, and Product Marketing. In this position, you will have the opportunity to create new capabilities on the Berkeley Lights Platform, taking products from early conception through product launch. Responsibilities: End-to-end workflow development involving precious sample handling, microfluidic-based workflow development, and workflow automation. Validation and verification of complex life science instrumentation. Contribution to the invention of core intellectual property (from conception through validation), white papers, and external publications. | 12/31/2020 |
| 55 | BioAssay Systems Hayward, CA Research Associate - Assay Development BS in Biochemistry, Chemistry, Biology, or Related Exp: 1-2 Years |
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. | 12/31/2020 |
| 56 | BioAssay Systems Hayward, CA Research Associate - Manufacturing BS in Biochemistry, Chemistry, Biology, or Related Exp: 1-2 Years |
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. | 12/31/2020 |
| 57 | Bioclinica Newark, CA Clinical Data Manager BS in Computer Science, Life Science, or Related Exp: 1+ Years |
Responsibilities: Understanding the requirements for study implementation and data collection. Collaborating with project team to develop study-specific edit check criteria. Defining, running, and reviewing edit checks and resolving discrepant data. Maintaining organized, complete, and up-to-date study documentation. Performing study setup, including TF design, database structure, specifications, and obtaining and providing approvals as needed. Coordinating and documenting the receipt and processing of electronic or ancillary data received from outside sources (e.g., data received from other central laboratories, CRO's, or Sponsors). Keeping supervisor informed of project status. | 1/3/2021 |
| 58 | Bioclinica Princeton, NJ Medical Writer BS in Life or Physical Sciences Exp: 1+ Years |
Responsibilities: Performing new award tasks such as entering new studies into the MedComm database, creating Medical Affairs and Medical Communications study-specific folders, organizing study documents, requesting signed Protocols, entering document costs in the new award spreadsheet, and notifying assigned Project Teams. Performing a concise and thorough review of study Protocols related to imaging requirements, schedules and windows. Creating, modifying and finalizing Site Manuals, associated fillable forms, and labels. Creating, modifying and finalizing Study Start-Up related Compliance Reports (CRs) such as Protocol Amendment Impact Forms (PAIFs), Notes to File (NTFs), Corrections, non-Quality Event Deviation Reports, and Transfers of Obligation (ToO) as required/applicable. Creating, modifying and finalizing paper Source Documents/eCRFs for reads performed outside a standard application (e.g., based on ToOs) on an as-needed basis. Creating, reviewing, modifying and finalizing MedComm Meeting Minutes. | 1/3/2021 |
| 59 | Bioclinica Princeton, NJ Imaging Research Associate BS in Biological or Computer Science Exp: 0+ Years |
Responsibilities: Assist in preparation and reproduction of study materials during study start-up phase of clinical trials. Follow up with outstanding documentations from clinical sites to complete site qualification. Schedule logistical and technical trainings with site personnel. Create test run requests for sites submitting digital data. Review, process, track and monitor all study related data received from sites. Assist in the monitoring and resolution of data discrepancies resulting from discrepancy listings generated from clinical data management. Manage site communications, generate site and patient reports and queries, and verify reports prior to distribution to clinical sites and sponsors. Investigate and complete logistical edit checks. | 1/3/2021 |
| 60 | Bioclinica Princeton, NJ Clinical Project Manager BS in Life Sciences, Pharmacy, Nursing, or Related Exp: 1-3 Years |
Responsibilities: Reviewing study requirements and response assessment criteria and collaborates with key stakeholders to develop study start-up activities and associated documents. Defining project plans (i.e. timelines, milestones and limitations for project staff). Establishing project reporting schedules. Providing project updates to BD Director, Global Services Managing Directors, Sponsor representative(s) on schedule. Communicating timely, appropriate project information to project teams, sites and company/sponsor representative(s). | 1/3/2021 |
| 61 | Biodesix De Soto, KS Laboratory Assistant BS in Chemistry, Biology, or Life Science Exp: 0+ Years |
Responsibilities: Pickup, receiving and storage of clinical specimens (i.e., blood); accessioning specimens for clinical testing, making labels, setting up tubes and supplies, logging into the computer-based laboratory information system; inventory management support and general lab assistant type work (e.g., maintaining eye wash station, fire extinguishers, shower, stockroom, etc.). | 1/3/2021 |
| 62 | Biodesix Boulder, CO Test Processing Specialist I BS in Relevant Discipline Exp: 1-3 Years |
Responsibilities: Data entry of test information. Confirmation of entered data, and confirmation that data provided meets the minimum requirements as indicated by the QMS. Timely and accurate delivery of reviewed test results. Participation in quality and accuracy programs. Other duties as assigned. | 1/3/2021 |
| 63 | Amunix San Francisco, CA Research Associate, Bioanalytical Sciences MS in Scientific Discipline Exp: 1+ Years |
The successful candidate will be responsible for developing and qualifying Ligand Binding Assays (e.g. ELISA, ECL), quantitative Westerns and/or Cell-Based Assays for pharmacological (PK, PD, and ADA) assessments to help advance research, pre-clinical, and clinical stage programs. The incumbent will analyze pre-clinical study samples using Ligand Binding Assays, cell-based assays, Luminex and/or quantitative Western. This list contains the major duties and requirements of the job and is not all-inclusive. Incumbent(s) may be expected to perform role-related duties other than those contained in this document. | 12/9/2020 |
| 64 | Analogic Peabody, MA EHS Specialist BS in Environmental, Occupational Health, Safety, Science, or Engineering Related Field Exp: 1-3 Years |
The EHS Specialist will report to the EHS Manager and be responsible for supporting and implementing effective safety and environmental guidelines, policies, and programs that will maintain a safe workplace and meet environmental objectives. The EHS Specialist will assist in maintaining corporate compliance with all appropriate EHS related governmental regulations. At the federal level, this includes OSHA, EPA, RCRA, CERCLA, and SARA. State regulations include Department of Labor and Industries (DLI), the Department of Public Health (DPH), the Department of Environmental Protection (DEP), and Workers Compensation under Department of Labor (DoL). Local community regulations include building and public safety ordinances. | 12/16/2020 |
| 65 | ANI Pharmaceuticals Baudette, MN Analytical Development Chemist BS in Chemistry, Biochemistry, Microbiology or Related Exp: 1-3 Years |
Responsibilities: Perform testing on raw material, in-process, and finished product samples. Execute compendial method verifications, method transfers and validation in support of new product development. Set-up and confirm suitable operation of equipment and instrumentation. Collect data and generate and report results in accordance with governing test methods and SOPs. Work with management in the vent of discrepancies. Perform review of data collected under approved test methods and investigational plans and protocols, in accordance with governing SOPs. Provide accurate assessment of data integrity, and document findings. Work with management and peers to correct deficiencies. Perform calibrations, preventive maintenance, and repairs as needed on instrumentation. Qualify new equipment as assigned. | 12/16/2020 |
| 66 | ANI Pharmaceuticals Baudette, MN QC Chemist BS in Chemistry, Biochemistry, Microbiology or Related 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. | 12/16/2020 |
| 67 | ANI Pharmaceuticals Baudette, MN Quality Assurance Specialist I BS in Relevant Discipline Exp: 1 Year |
This position is responsible for providing support to the Manufacturing and Packaging Operations to ensure relevant procedures are followed and meet GMP requirements. Other responsibilities: Perform Packaging Line inspection/audits and provide assurance that packaging operations are compliant with applicable SOPs and GMPs. 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 samples stored in the reserve sample room. Perform Complaint writing. Monitor GMP areas for compliance with general GMP requirements such as proper gowning and cleanliness. | 12/16/2020 |
| 68 | Applied Medical Rancho Santa Margarita, CA Quality Engineer BS in Engineering or STEM Field Exp: 1-2 Years |
As a Quality Engineer II, you will use your skills to support medical device quality through design controls, process validations and documentation as part of a cross-functional team. Responsibilities: Conduct experiments to prove hypotheses. Create and validate test methods for design verification and manufacturing inspection testing by using measurement system analysis, gauge R&R and other relevant techniques. Implement statistical techniques to determine sample sizes and levels of confidence. Implement statistical process controls to monitor validated processes. Design engineering test protocols and use a data-driven approach to collect, analyze and summarize data into engineering reports. Perform root cause investigations for design and manufacturing. Document Non-Conformance Investigations (NCIR). | 12/16/2020 |
| 69 | Applied Medical Rancho Santa Margarita, CA Electrical Engineer I 4 Year Degree in Computer Engineering, Electrical Engineering, or Related Exp: 0-3 Years |
As a Electrical Engineer you will be responsible for working within the framework of a team and performing the following activities: Schematic design of new and innovative projects. Analyze the hardware and firmware of embedded medical electrical systems with an emphasis on power management, digital and analog controls, and low frequency (500 kHz) high power (500 W) RF amplification. Participate in firmware creation for programmable logic devices such as DSPs, FPGAs, and CPLDs. Participate in hardware and firmware design reviews. Provide design know how for external vendors and supplier development. Support other groups during integration of hardware, firmware, and software. Test and troubleshoot boards and system level electrical systems. Develop, update, and peer-review engineering documents such as instructions, drawings, test procedures and reports. | 12/16/2020 |
| 70 | Applied Medical Rancho Santa Margarita, CA Process Engineer II BS in Mechanical, Biomedical, Industrial, or Manufacturing Engineering Exp: 1-2 Years |
As a Process Engineer II, you will use skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. Responsibilities: Develop and sustain manufacturing processes. Debug manufacturing processes and equipment via root cause analysis. Run, observe and expedite shop orders. Develop and update engineering documents such as process maps, process FMEA, Manufacturing / Quality Instructions, Test Methods, drawings, and Test Reports. Collaborate with production to identify capabilities and capacity/ Collaborate with engineering team for fixturing design and development, tolerancing, and design for manufacturing. | 12/16/2020 |
| 71 | Applied Medical Rancho Santa Margarita, CA R&D Engineer II BS in Mechanical, Biomedical, Industrial, or Manufacturing Engineering Exp: 1-2 Years |
As a R&D Engineer II, you will use skills related to design and development of medical device components and fixtures as part of a cross-functional team. Responsibilities: Create Solidworks models, drawings and assemblies. Build functional prototypes for device development. Perform engineering testing. Debug via root cause analysis. Investigate new tooling, materials, manufacturing processes and technologies. Research and qualify new suppliers and vendors. Complete documentation of design efforts for the Design History File. Develop, update, and peer-review engineering documents such as instructions, drawings, test procedures, and reports. Collaborate with tooling design teams (MIM, Stamping, Molding, etc.). | 12/16/2020 |
| 72 | Applied Medical Rancho Santa Margarita, CA Complaint Evaluation Engineer BS in Mechanical Engineering, Biomedical Engineering, Electrical Engineering, or Related Exp: 1+ Years |
As a Complaint Evaluation Engineer, you will be responsible for working within the framework of a team and performing the following activities: Evaluate the performance of products returned by the customer. Perform device analysis in accordance with model-specific procedures and protocols. Perform root cause analysis to investigate alleged product deficiencies. Propose corrective/preventive actions as required. Compose detailed reports describing results from investigations. Complete evaluations in a timely and accurate manner. | 12/16/2020 |
| 73 | Applied Medical Rancho Santa Margarita, CA CNC Machine Operations Engineer BS in Mechanical, Industrial, or Manufacturing Engineering Exp: 1-2 Years |
As a CNC Machine Operations Engineer, you will use skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. Responsibilities: Develop and sustain manufacturing processes. Debug manufacturing processes and equipment via root cause analysis. Run, observe and expedite shop orders. Develop and update engineering documents such as process maps, process FMEA, Manufacturing/Quality Instructions, test methods, drawings, and test reports. Collaborate with the Production team to identify capabilities and capacity. Collaborate with the Engineering team for fixturing design and development, tolerancing, and design for manufacturing. Collaborate with tooling design teams (MIM, Stamping, Molding, etc.). Investigate new tooling, materials, manufacturing processes, and technologies. Research and qualify new suppliers and vendors. | 12/16/2020 |
| 74 | Applied Molecular Transport San Francisco, CA Upstream Manufacturing Associate BS in Chemical Engineering, Microbiology, Biochemistry, or Related Exp: 0-2 Years |
AMT is looking for an Upstream Manufacturing Associate to work in our GMP manufacturing facility to produce biopharmaceutical proteins. The primary focus of the Manufacturing Associate role will be work as part of a team to conduct GMP upstream manufacturing production assignments and tasks with high quality and timely output. Responsibilities: Set-up and operation of single-use fermentation, cell processing, and separation equipment. Process monitoring and sampling, including performing routine sample analysis. Weigh out chemicals, prepare media, solutions, and buffers. Participation in daily operation and routine maintenance of process and analytical equipment. Maintaining a clean and organized lab environment. Chemicals and consumables stocking, etc. Maintaining strict adherence to batch records, SOP’s, and safety guidelines designate for the manufacturing process. | 12/16/2020 |
| 75 | Applied Molecular Transport San Francisco, CA Scientist/Sr. Scientist BS/MS in Chemistry, Biochemistry, Biological Sciences, Pharmaceutical Sciences, or Related Exp: 1-5 Years |
The Scientist/Sr. Scientist position is within AMT’s analytical development group that is based at Tower Place, South San Francisco. In this role, the scientist will perform method development, qualification, and technology transfer for the release and stability testing of drug substance and drug products. The position will report to Director of Analytical Development and collaborate with cross-functional teams at AMT. Responsibilities: Perform analytical method development for LC based assays such as SEC, IEX and reversed-phase HPLC, and other protein-based analysis (i.e. SDS-PAGE, CE-SDS, A280, etc.). Provide testing support for the in-house manufacture of drug substance and drug product. Execute stability studies to evaluate and characterize protein degradation during storage. Process data and present findings at regular team meetings. Document operating procedures for technology transfer and work to implement methods in a GMP environment. | 12/16/2020 |
| 76 | Arcus Biosciences Hayward, CA Research Associate/Sr. Research Associate, Immunology BS in Cell Biology, Immunology, or Related Exp: 1-2 Years |
The Biology group is seeking a motivated, energetic, and skilled individual who wishes to play a role in advancing novel immunotherapy drug candidates from the discovery phase into the clinic. The role will be responsible for executing a variety of experiments using in vivo models and in vitro assays in order to validate new targets and understand mechanism of action and pharmacodynamic properties of drug candidates. A successful candidate will contribute as part of a multidisciplinary team in a fast-paced environment to plan and execute experiments and subsequently collate, document, interpret, and present data internally. | 12/16/2020 |
| 77 | Arcus Biosciences Hayward, CA Sr. Clinical Data Analyst BS/MS in Statistics, Epidemiology, Bioinformatics, or Related Exp: 0-4 Years |
The Sr. Clinical Data Analyst will be responsible for creating fit-for-purpose analyses, visual data displays and dashboards from diverse data types to aid in internal data consumption and decision-making. This position will report into the Head of Statistical Programming and will interact regularly with diverse stakeholders across the organization. Demonstrated abilities to prioritize work; to understand internal business, data and decision-making needs; and to communicate and collaborate with key stakeholders both within Biometrics and beyond (research, translational science, clinical science, clinical operations, safety, medical affairs and commercial) are essential. | 12/16/2020 |
| 78 | Arcus Biosciences Hayward, CA RA - Lead Discovery and Optimization BS/MS in Biochemistry, Chemical Biology, Molecular Biology, or Related Exp: 0-3 Years |
Arcus is seeking self-motivated, collaborative and highly skilled individuals to work with them to discover novel anti-inflammatory and immunotherapeutic oncology drugs. The opening for an enthusiastic and motivated research associate requires the application of creative problem-solving approaches to the execution of biochemical and cell-based assays to provide insightful SAR (structure activity relationship). The successful candidate will be a rigorous, quantitative, detail-oriented experimentalist coupled with excellent practical laboratory skills and enthusiasm for automated laboratory assay techniques. Responsibilities: Executing micro-plate-based in vitro biochemical and cell-based enzymatic and ligand binding assays. Maintaining mammalian cell culture and conducting transient and stable mammalian cell protein expression. Utilizing liquid handling systems and laboratory robotics to implement in vitro. Performing practical laboratory work, managing day to day tasks and ensuring timely delivery of high-quality results. | 12/16/2020 |
| 79 | Arcus Biosciences Hayward, CA Research Associate BS/MS in Molecular Biology, Biochemistry, or Related Exp: 0-3 Years |
This position requires the application of creative problem-solving approaches to the execution of new biochemical and cell-based assays. The successful candidate will have excellent practical laboratory skills, coupled with aptitude and enthusiasm for automated laboratory assay techniques. Responsibilities: Performing routine assays to support chemistry efforts. Execution of new biochemical and cell-based assays. Practical laboratory work, managing day to day tasks and ensuring timely delivery of high-quality results. Utilizing liquid handling systems and laboratory robotics to implement in vitro. Contribute during lab meetings and assist in the analysis and reporting of experimental data to project teams. | 12/16/2020 |
| 80 | Arcus Biosciences Hayward, CA Research Associate: Lead Discovery and Optimization BS/MS in Molecular Biology, Biochemistry, or Related Exp: 0-3 Years |
The RA Lead Discovery and Optimization position requires the application of creative problem-solving approaches to the execution of new biochemical and cell-based assays. The successful candidate will have excellent practical laboratory skills, coupled with aptitude and enthusiasm for automated laboratory assay techniques. Responsibilities: Performing routing assays to support chemistry efforts. Execution of new biochemical and cell-based assays. Practical laboratory work, managing day to day tasks and ensuring timely delivery of high-quality results. Utilizing liquid handling systems and laboratory robotics to implement in vitro. Contribute during lab meetings and assist in the analysis and reporting of experimental data to project teams. | 12/16/2020 |
| 81 | Argonaut Manufacturing Services Carlsbad, CA Technical Transfer Operator, Drug Product Manufacturing BS in Life Science or Engineering Discipline Exp: 1-3 Years |
The purpose of this position is to transfer product and process knowledge from developmental clinical production to GMP product manufacturing in the drug product manufacturing division of Argonaut. Responsibilities: Facilitate transfer of new processes from client lab or concept to drug product manufacturing by collaborating with subject matter experts and operations management. Participate in client discussions via phone, video conference, and/or onsite visits. Create and revise client-specific batch records, raw material specifications, and any documentation related to Drug Product Manufacturing. Review executed batch records and other documentation, as needed. Track and trend documentation issues. | 12/16/2020 |
| 82 | Argon Medical Devices Athens, TX Manufacturing Engineer I BS or Higher in Mechanical or Industrial Engineering Exp: 1-2 Years |
The Manufacturing Engineer will work to gather and document customer requirements, translate them into measurable product requirements, and provide engineering support for the development and manufacture of Argon Medical Device products. The Manufacturing Engineer will recommend, develop, and implement manufacturing-related cost-saving initiatives (Value Improvement Projects) and be responsible for developing and implementing product qualification protocols. The Manufacturing Engineer will confer with vendors to determine product specifications and arrange for purchase of equipment, materials, or parts and evaluate products according to specifications and quality standards, including assisting in the estimation of production times, staffing requirements, and providing related costs information for management decisions. | 12/16/2020 |
| 83 | ARL Biopharma Oklahoma City, OK Laboratory Technician - Microbiology Lab BS in Microbiology or Related Exp: N/A |
This job operates in a laboratory environment. Attendance at the office is required. While performing the duties of the job the employee is frequently exposed to various microorganisms and may be exposed to toxic or hazardous chemicals. The employee will be required to wear all appropriate safety equipment including but not limited to eye protection, gloves, full face respirator and lab coat. This role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines. Responsibilities: Media preparation, glassware cleaning, inventory / ordering, lab cleaning and sanitization, and autoclaving various reagents and supplies. Assist laboratory personnel in daily activities to maintain high scientific quality and compliance with SOPs, protocols, and safety standards. | 12/16/2020 |
| 84 | ARL Biopharma Oklahoma City, OK Laboratory Technician - R&D Lab BS in Chemistry or Related Exp: N/A |
R&D Lab Tech performs general laboratory tasks under immediate supervision. The work involves preparation of chemical reagents/mobile phase, assistance with chemical tracking/disposal, and assistance with sample retrieval, preparation and storage. The position requires ability to use a personal computer, including familiarity with word processing, spreadsheet, email and database applications. Responsibilities: Prepare chemical reagents/mobile phase. Assists chemical tracking/disposal. Assists sample retrieval, preparation and storage. Order and organize general lab supply. Wash glassware and maintain lab cleanness. | 12/16/2020 |
| 85 | ARL Biopharma Oklahoma City, OK Laboratory Technician - Analytical Lab BS in Chemistry or Related Exp: N/A |
Responsibilities: Adhere to Quality Management System (QMS). Follow prescribed safety rules and regulations in performing all assigned duties. Follow written and oral instruction. Prepare reagents, solutions, and mobile phases required for testing. Perform timely peer review of laboratory notebooks. Sample management including retrieval, storage, and disposal. Work and think independently, yet share ideas and work towards team goals. Use a personal computer including word processing, spreadsheets, email and database applications. Express thoughts in a clear concise manner both orally and written. Work to establish the ability to effectively prioritize and plan multiple work activities with varying deadlines and complexities. Ability to wear, maintain, and properly use appropriate safety equipment, including, but not limited to eye protection, gloves, and lab coat. Adherence to all ARL Bio Pharma safety standards, policies, procedures, and protocols. | 12/16/2020 |
| 86 | Arraystar Inc Rockville, MD Lab Assistant - Molecular Biology BS in 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. | 12/16/2020 |
| 87 | Arthrex Naples, FL Associate Product Manager - Imaging BS/MS in Relevant Discipline Exp: 1 Year/0 Years |
The Associate Manager plans, organizes, and controls an assigned product line from conceptual stages through product life cycles to optimize profit and meet marketing, financial, and corporate growth objectives by performing the following duties. Responsibilities: Participates in overall marketing, product strategy, research and development requirements, development, and manufacturing coordination for new and emerging products. Works on technical product development, estimates of potential profits, and release to production. Assists in the management of day-to-day progress and maintenance of products. Provides technical expertise and training to other departments in support of product development. Works with Product Team to develop marketing analysis to determine product definitions. | 12/16/2020 |
| 88 | Arthrex Naples, FL Associate Product Manager - Fluid Management BS/MS in Relevant Discipline Exp: 1 Year/0 Years |
Responsibilities: Participates in overall marketing, product strategy, research and development requirements, development, and manufacturing coordination for new and emerging products. Works on technical product development, estimates of potential profits, and release to production. Assists in the management of day-to-day progress and maintenance of products. Provides technical expertise and training to other departments in support of product development. Collaborates with a wide variety of functional areas such as sales, engineering, marketing, manufacturing, and operations to develop and provide product definitions responsive to customer needs and market opportunities. Provides financial and technical justification for product selection and definition. Conducts market research and identifies and tracks market trends in company's industry. Produces competitive analysis materials comparing product with its key competitors. Participates in key sales situations for the product. Works with PM to define promotional activities, publicizing the product through the press, sales force, and alternate distribution channels. | 12/16/2020 |
| 89 | MeiraGTx New York City, NY Research Associate, Molecular and Protein Engineering BS in Life Science Discipline Exp: 0-2 Years |
MeiraGTx is seeking a motivated, enthusiastic, well-rounded individual with experience in molecular biology and biochemistry to be a part of an early pre-clinical stage Molecular and Protein Engineering group to develop better, smarter gene therapies. For this position, under the guidance of senior scientists, the successful candidate will be primarily responsible for the general laboratory upkeep of the research group and assisting in the construction of mammalian plasmids harboring engineered transgene cassettes, performing transient expressions of said plasmids in relevant mammalian cell lines, and subsequent testing of the expressed transgenes for improved functions using in vitro biochemical and/or cell-based assays. | 12/16/2020 |
| 90 | MeiraGTx New York City, NY Technician, Molecular and Protein Engineering BS in Life Science Discipline Exp: 0-2 Years |
MeiraGTx is seeking a motivated, enthusiastic, well-rounded individual with experience in molecular biology and biochemistry to be a part of an early pre-clinical stage Molecular and Protein Engineering group to develop better, smarter gene therapies. For this position, under the guidance of senior scientists, the successful candidate will be primarily responsible for assisting in the construction of mammalian plasmids harboring engineered transgene cassettes, performing transient expressions of said plasmids in relevant mammalian cell lines, and subsequent testing of the expressed transgenes for improved functions using in vitro biochemical and/or cell-based assays. | 12/16/2020 |
| 91 | MeiraGTx New York City, NY Technician, Molecular and Protein Engineering BS in Molecular Biology, Cellular Biology, or Related Exp: N/A |
MeiraGTx is seeking motivated and enthusiastic technicians to join their growing research and development team. The applicant should have experience using standard molecular and cellular biology techniques, will be required to present results and updates at project team meetings, maintain accurate and well-organized experiment records. The qualified candidate will work independently and as part of a team to closely collaborate with other team members. Responsibilities: Maintain cultures of mammalian cell lines. Plasmid DNA extraction and purification, quantification. Perform cell-based assays, high throughput screening. Analyze, interpret and present experimental results accurately, maintain clear and up-to-date experiment records. | 12/16/2020 |
| 92 | Aruna Bio Athens, GA Biomanufacturing Associate BS in Biological Science, Cell Biology, Biomedical Engineering, or Related Exp: 0-2 Years |
The Biomanufacturing Associate supports the the manufacturing efforts of ArunA Bio, and must work collegially and collaboratively as part of a larger team. The position requires the individual to carry out complex stem cell manufacturing with an advanced degree of detail, and in accordance with established SOPs, cGMPs, and safety regulations. The individual will work as a member of a team responsible for performing all bioprocessing workflows. | 12/16/2020 |
| 93 | Atara Bio Thousand Oaks, CA Manufacturing Associate BS in Scientific Discipline Exp: 0-2 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. Responsibilities: Support production in an aseptic environment. Executes on production batch records and work orders according to SOPs. Assist in all areas of cell culture and all related duties as required including (stocking, tracking inventory, material movement, maintaining metrics, filling out log sheets, and other special projects). Assists in manufacturing batch record review. Routine maintenance and cleaning of rooms and equipment. Identifies and implements continuous improvements. Perform tasks in a manner consistent with the safety policies, quality systems, and GMP requirements. Adhere to all safety protocols and procedures. | 12/16/2020 |
| 94 | Atara Bio Thousand Oaks, CA Research Associate - CAR-T Development BS in Cell Biology, Immunology, Molecular Biology or Related Exp: 1+ Years |
The Research Associate - CAR-T Development is an integral member of the Preclinical Immunotherapy Research group. This role will be responsible for the generation and characterization of novel CTL and Chimeric Antigen Receptor (CAR) T cell therapies. The successful candidate will perform experiments to support new product development and IND-enabling activities for Atara’s CAR T cell pipeline. Other responsibilities: Performs retroviral (gamma retrovirus and/or lentiviral) transductions of primary T cells and propagation. Evaluates allogeneic CAR T cell activity, efficacy, and alloreactivity. Performs primary immune cell isolation and multi-parameter immunophenotyping by flow cytometry. Designs and executes assays to evaluate target-specific T cell characteristics and function. | 12/16/2020 |
| 95 | Atara Bio Thousand Oaks, CA Research Associate Viral Vector Process Development BS in Relevant Discipline Exp: 1+ Years |
The Viral Vector Process Development Research Associate is an active member of a growing viral vector process development team supporting Atara’s T-cell therapy programs. The individual will contribute to the development, scale up and technology transfer of the viral vector production with focus on cell culture development and scale-up. These activities can include aseptic cell culture of viral vector suspension and/or adherent cell lines, scale-down model and qualification, scale-up development, process optimization, robustness studies, and process characterization. Experience with both suspension and adherent formats are desired. This position includes viral seed stock production, viral vector production and purification, virus process development and scale-up, and analytical testing of in-process controls. | 12/16/2020 |
| 96 | Atara Bio Thousand Oaks, CA Associate Scientist - Analytical Development MS in Biological Sciences Exp: 1-5 Years |
The Associate Scientist will work with the Analytical Development team to develop and execute analytical methods to characterize T cell therapy manufacturing processes and products across the Atara EBV T-cell platform, with an emphasis on flow cytometric methods for characterization and lot release. The candidate will design and execute experiments, organize, document, analyze and interpret results using sound scientific principles. The candidate will present data to cross-functional teams, and thus strong written and verbal communication is essential. | 12/16/2020 |
| 97 | Athenex Clarence, NY Quality Control Laboratory Technician BS in Chemistry or Related Exp: 6+ Months |
The technician will support the laboratory workflow in an efficient and effective manner and support the analytical group in maintaining the laboratory to make workflow more efficient. Responsibilities: Promoting and maintaining safe and healthy working conditions in his I her assigned work area; instructs and enforces compliance with established safe work practices and procedures. Properly disposes of solvent waste in appropriate containers and disposes of empty bottles in the recycling bins according to health, safety and environmental practices. Performs laboratory, office and maintenance on a routine basis. Performs and documents periodic checks of the eye wash stations located in the laboratory. | 12/16/2020 |
| 98 | Atreca San Francisco, CA Research Associate I/II, in vitro Pharmacology BS in Cell Biology, Immunology, or Related Exp: 1+ Years |
Atreca is seeking a Research Associate (RA) who will apply her/his skills in cell biology and flow cytometry to screen the growing library of Atreca antibodies for binding against tumor cells. The successful candidate will work in a fast-paced and team-based environment with opportunities to collaborate across different functional groups within the organization. Responsibilities: Harvest and stain cells for screening using flow cytometry in a high throughput format. Flow data analysis and quality control and assay optimization. Follow laboratory safety guidelines and practices. | 12/16/2020 |
| 99 | Atreca San Francisco, CA Research Associate - Molecular Biology BS/MS in Molecular Biology or Related Exp: 0-3 Years |
Atreca is seeking a highly skilled candidate to apply her/his skills to discover novel anti-cancer biologics by leveraging the cancer patient immune response. This will include using molecular biology skills to build and sequence patient antibody repertoires and perform interrogations using antibody display and selection techniques. The successful candidate will become a key member of the R&D team, deeply involved in experimental planning, troubleshooting, and execution. She/he will perform experiments, analyze data, and present her/his research findings to interdisciplinary teams. Strong analytical skills, excellent written and verbal communication skills, and attention to details are extremely important for this position. | 12/16/2020 |
| 100 | Atreca San Francisco, CA Senior Research Associate, Protein Engineering MS in Cell Biology, Immunology, Bioengineering or Related Exp: N/A |
The successful candidate will play a key role producing and characterizing antibodies and engineered bispecifics in support of pre-clinical studies. This position will have the opportunity to interact and collaborate with a multidisciplinary team and utilize a variety of biophysical techniques to characterize novel therapeutics. Responsibilities: Scout small-scale productions and develop new purification methods to support scale ups of novel therapeutics (antibodies and bispecifics). Produce and purify novel therapeutics at multi-Liter scale for use in pre-clinical studies. Develop and perform analytical methods, including SEC, IEX, HIC, MALS, BLI, SPR, Tm/Tagg and SLS/DLS. | 12/16/2020 |
| 101 | AtriCure Mason, OH Regulatory Affairs Specialist BS in Relevant Discipline Exp: N/A |
This position will originate appropriate documents to obtain and maintain marketing privileges consistent with applicable government requirements where AtriCure conducts business. This position will also maintain internal documentation of such approvals and handle requests for documentation from our international distributors and customers. This position is responsible for practicing Quality System Manual procedures and complying with its requirements, and carrying out responsibilities as outlined in safety, health and environmental policies. | 12/16/2020 |
| 102 | ATUM Newark, CA Cell-Line Development Associate BS/MS in Biology, Molecular Biology, Cell Biology, Biochemistry, or Related Exp: 1+ Years |
ATUM is in need of an experienced Cell-Line Development Technician to join their team and help lead the development of their growing Cell Line Development Division. You’ll be a key part of the production process and have the opportunity to work with multiple departments in a fun and collaborative work environment. The successful candidate should possess: Excellent hands-on tissue culture experience with HEK and CHO cell-lines. A proven track record in an industrial setting in the development of enhanced mammalian expression platforms through host cell line engineering strategies. Successful experience generating stable cell lines for protein expression. The ability to work collaboratively within and across departments. | 12/16/2020 |
| 103 | ADMA Biologics Boca Raton, FL QA Specialist II - Quality, Engineering, Validation BS in Relevant Discipline Exp: 1-5 Years |
The QA Specialist II-Quality, Engineering, Validation will Perform a wide variety of Quality Assurance activities to ensure compliance with related regulatory requirements. Primarily responsible for the efficacy and compliance of the change control management system, validation and qualification systems, Corrective and Preventive Action reports (CAPA) and Risk Management policies and procedures. Other responsibilities: Ensure cGMP and regulatory compliance as defined in government regulations such as 21 CFR Parts 11, 210, 211, and 600, as well as compliance with corporate policies and procedures. Perform QA review and approval of Change Control and Corrective Action Preventive Action (CAPA) Quality Systems. Independently assess required supporting documentation to support change and corrective/preventive actions. Assist in the Change Review Board (CRB) to ensure that changes are initiated, evaluated, properly classified, authorized and implemented in accordance with Regulatory and Corporate requirements. | 12/2/2020 |
| 104 | ADMA Biologics Boca Raton, FL Technician I, Manufacturing Purification BS in Chemistry or Life Science Exp: N/A |
This position is under direct supervision of the Group Leader. It is mainly responsible for the manufacturing of plasma products through protein precipitation/separation and other tasks involving plasma receipt, plasma pooling, and protein separation. The Protein Purification Manufacturing Technician will also clean and sanitize equipment before and after use, make and verify connections on flow panels, perform pH and conductivity measurements, performs chemical and buffer additions and may assist Group Leader in training other tech positions. | 12/2/2020 |
| 105 | Admera Health South Plainfield, NJ Associate Scientist I, Project Management BS/MS in Biological Sciences Exp: 1+ Years |
Responsibilities: Relay standard information on next generation sequencing applications to customers. Standard communication with prospective, current, and past customers. Co-coordinating multiple genomic projects with excellent documentation skills and communication to customers. Materials purchasing support for laboratory team. Collaborate within group to streamline incoming, ongoing, completed projects – minimally cross-departmental. Learn relevant next generation sequencing materials for RUO applications. Comply with all CLIA/CAP regulations. | 12/9/2020 |
| 106 | Admera Health South Plainfield, NJ Associate Scientist I/II - Lab BS/MS in Biological Sciences Exp: 1+ Years |
Responsibilities: Preparing solutions and reagents for performing assays on the bench. Perform Next Generation Sequencing-based genomic assays on different workflows: 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 record keeping of all laboratory procedures. Collaborate within the group and cross departmental to achieve goals. | 12/9/2020 |
| 107 | Akadeum Life Sciences Ann Arbor, MI Research and Development Scientist MS in Relevant Biological or Chemical Science Exp: 1 Year |
The ideal candidate will be comfortable working in a fast-paced, early stage company environment and will be flexible to accommodate shifting company priorities. The individual will independently design, execute, and analyze experiments to advance goals relative to specific projects as well as contribute to a variety of R&D responsibilities including routine lab maintenance, assay development and validation, quality control, and cross-departmental support. The ideal candidate is highly motivated and is willing to adapt to shifting priorities and switch between projects seamlessly. This position will fulfill a variety of roles instrumental to the successful development of Akadeum’s growing platform capabilities. | 12/9/2020 |
| 108 | Akoya Biosciences Marlborough, MA Associate Research Scientist MS in Cell Biology Exp: N/A |
As an Associate Reagent Scientist, 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. This position also includes working for the Quality team to provide technical support for new and on-market products QC. The desired skillset for laboratory work includes the ability to perform immunohistochemistry (IHC) procedures and analytical analysis for product development and product support. Your work will mainly involve manual laboratory work and the use of automated stainer systems for monoplex and multiplex fluorescence tissue staining. | 12/9/2020 |
| 109 | Alcami Wilmington, NC Assistant Scientist II BS in Pharmaceutical Sciences, Chemistry, or Equivalent Exp: 1-2 Years |
The Assistant 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 Analytical Assistant Scientist II may also assist with method development/method validation projects. Typical types of testing: assays (potencies, related substances, residual solvents, metals etc.), rate of release (dissolution), 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, 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. | 12/9/2020 |
| 110 | Alcami Durham, NC Assistant Scientist II BS in Pharmaceutical Sciences, Chemistry, or Equivalent Exp: 1-2 Years |
The Assistant 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 Analytical Assistant Scientist II may also assist with method development/method validation projects. Typical types of testing: assays (potencies, related substances, residual solvents, metals etc.), rate of release (dissolution), 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, 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. | 12/9/2020 |
| 111 | Alcami Wilmington, NC Associate Scientist MS In Pharmaceutical Sciences, Chemistry, or Equivalent Exp: N/A |
The Associate Scientist may be required to work on method development/method validation projects. For this position HPLC 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. | 12/9/2020 |
| 112 | Alcami St. Louis, MO Chemistry Quality Specialist II MS in Chemistry, Biology, or Related Exp: 1+ Years |
The Chemistry Quality Specialist II is accountable for activities which may include reviewing documents and data, conducting basic floor audits and processes 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 II 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. | 12/9/2020 |
| 113 | Aldevron Fargo, ND Associate Process Validation Specialist BS in Biology, Biochemistry, Engineering, or Related Exp: N/A |
The Associate Process Validation Scientist supports internal and external Process Validation and Robustness activities with projects focused on understanding and reducing process variability to improve product quality, cost, and process efficiency. This position also supports Cleaning Validation and Facility Environmental Monitoring Qualifications to ensure the production environment is compliant with regulatory requirements. Other responsibilities: Work collaboratively to design, conduct, and report findings on experiments characterizing new or changed manufacturing processes and new equipment or technology. Support continuous improvement projects addressing process variability, efficiency, product cost and data analysis. Compile, maintain and analyze critical data supporting R&D, engineering and validation work. Execute and/or coordinate execution of process, cleaning, shipping and continued process verification activities. | 12/9/2020 |
| 114 | Aldevron Fargo, ND Lab Technician III - GMP BS Preferred Exp: 1+ Years |
The Lab Technician will work daily within Aldevron’s labs performing tasks associated with Aldevron’s GMP-Source services. The Lab Technician is expected to become familiar with all Aldevron’s products and to be able to perform most tasks associated with the purification of plasmid DNA. Other responsibilities: Detailed, thorough cleaning, line clearance, and segregation of GMP-Source production areas and associated equipment while wearing appropriate gowning. Training of Lab Technician II personnel. Assist in completing component list compilation as needed. Initiation and completion of deviation forms and Corrective Action documents. Organization and planning of buffer preparation area. | 12/9/2020 |
| 115 | Aldevron Madison, WI Metrology Technician BS in Metrology or Medical Equipment Technology Preferred Exp: 1-3 Years |
The Metrology Technician will ensure that all equipment is installed, qualified, maintained and calibrated properly, on schedule and complying with any industry or site standards. This position is responsible for performing a wide variety of activities following site operational and safety procedures in a laboratory and manufacturing setting. Work will include mechanical service calls, inspections and in-house repairs and preventive maintenance throughout the facility. Other responsibilities: Perform a variety of installation, maintenance, troubleshooting and repair duties on the facility and lab equipment, as assigned. Perform routine calibration, preventive and scheduled maintenance to ensure compliance of the equipment/system for its intended use is maintained and that manufacturing operational requirements are met. Schedule outside venders to preform maintenance and calibration and ensure that tasks are completed on time. | 12/9/2020 |
| 116 | Aldevron Fargo, ND mRNA Biomanufacturing Operator BS in Life Sciences Exp: 6+ Months |
The mRNA Biomanufacturing Operator II will work daily within Aldevron’s manufacturing labs performing tasks associated with the production of mRNA. Initially this individual will perform manufacturing for research grade and GMP while learning the production of mRNA. This planning for production activities, performing upstream and/or downstream tasks, and documenting production activities. This role reports into R&D. Other responsibilities: Perform various manufacturing tasks in accordance with Aldevron Standard Operating Procedures. Review daily work instructions and organize individual daily workflows. Document manufacturing activities on the Aldevron Internal Database. Complete work independently under daily written direction from the Production Supervisor(s). | 12/9/2020 |
| 117 | Alira Health Framingham, MA Business Development Associate, Clinical BS/BA in Business or Science Exp: 1-2 Years |
The Associate, Clinical Development is an important member of the Alira Health Clinical team. The Associate will be responsible for facilitation and tracking of all client outreach and will attend client meetings (both in person and remotely). The Associate works closely with the Manager of Clinical Development and will provide administrative support in identifying target clients, potential markets, and tracking related information. As a junior member of the Clinical Development team, the Associate will take on additional tasks as needed, including creation of client-facing materials and presentations and may attend industry conferences as needed. This position includes some travel. Other responsibilities: Assist with the development new business for Alira Health’s regulatory, clinical, and market access practices. Demonstrate an understanding of Alira Health’s range of services, with a focus on regulatory clinical trial, and market access services. Schedule and participate in new client teleconferences and meetings, acting as a facilitator for the senior Clinical Development team members. Track current and past clients, including follow-up, deadlines, and metrics, utilizing Salesforce and other tools. | 12/9/2020 |
| 118 | Alira Health Framingham, MA In-House Clinical Research Associate BS/BA in Relevant Discipline Exp: 1-2 Years |
The In-house Clinical Research Associate (In-house CRA) is an important member of the Alira Health Clinical team. In-house CRAs manage and support clinical sites from site approval through close-out. In-house CRAs work closely with field CRAs and Project Managers without the need for frequent travel. Other responsibilities: Develops study documents and tools, including Informed Consent Form (ICF) templates (for both local and central IRBs), site binder contents, tip cards, etc. Supports sites in obtaining IRB approval, developing submission materials, and creating site-specific ICFs. Responds to sites’ regulatory board requests for protocol and ICF clarification as needed. Ensures all required site regulatory documents and approvals are in place prior to investigational product shipment. | 12/9/2020 |
| 119 | Allogene Therapeutics San Francisco, CA Associate Scientist, Process Development BS/MS in Chemical Engineering, Biochemistry, Molecular Biology, Cell Biology, Immunology, or Related Exp: 1+ Years |
Allogene is current seeking a highly motivated Associate Scientist to join an exciting team in the allogeneic cell therapy industry. This is a 6+ month contract opportunity in the Process and Product Development group. Responsibilities: Support formulation & drug product development activities for allogeneic CAR T cell therapy products. Actively contribute to drug product process development and characterization. | 12/9/2020 |
| 120 | Almac Durham, NC Project Coordinator, Distribution BS in Business or Science Exp: 6+ Months |
The Project Coordinator - Distribution supports the Project Manager - Distribution by providing a back-up resource, in addition to managing some accounts themselves. The main objective of the position is to interpret customer supplied information and transform it into instructional documentation for operational distribution staff to complete shipments. The principal function of the project services department is the day-to-day management of all customers across any Almac Clinical Services (ACS) site. Responsibilities: In charge of interpreting customer supplied information, defining requirements, and generating associated documentation to support operational distribution staff in the shipment of finished goods, components, and ancillary items. The Project Coordinator - Distribution will assist the Project Manager - Distribution with all tasks associated with the successful management of the distribution and return of clinical trial supplies. Generate instructions for return, accountability and destruction at Almac facilities and Almac contracted depots. | 12/9/2020 |
| 121 | Almac Audubon, PA QC Inspector BS in Scientific Discipline Exp: 1+ Years |
The Quality Control Inspector will provide support to the QC analysts and ensure that all QC tasks are completed on time and are within Good Laboratory Practice. They will also carry out sampling and testing of packaging materials and sampling of starting materials and products and complete the required documentation according to specified standard operating procedures. Responsibilities: Sample starting materials and pharmaceutical products in line with approved SOPs. Perform finished goods inspections and conduct physical tests. Review results of testing carried out by other QC Inspectors. | 12/9/2020 |
| 122 | Almac Souderton, PA QC Inspector Grade 1, Incoming Goods BS in Scientific Discipline Exp: 1+ Years |
The QC Inspector Grade 1 – Incoming Goods will Sample, inspect and release incoming goods ensuring compliance with approved material specifications, cGMPs, SOPs, and other written quality standards. Responsibilities: Perform incoming goods sampling, inspection, and approvals in compliance with approved material specification, cGMP and Almac Clinical Services SOPs. Complete calibration checks on balances and scales. Sample clinical materials upon customer request. | 12/9/2020 |
| 123 | Alstem Cell Advancements Richmond, CA Research Associate BS/MS in Biochemistry, Molecular Biology, or Related Exp: 1+ Years |
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. | 12/9/2020 |
| 124 | Amarex Germantown, MD Clinical Data Coordinator BS in Relevant Discipline Exp: 1+ Years |
Responsibilities: Review and validate clinical trial data. Review case report forms and clinical data sets for errors, discrepancies and protocol violations. Ensure timely completeness and accuracy of databases. Adhere to company procedures related to data handling & data base validation. Implement data entry conventions. Organize and maintain clinical study databases to support regulatory submissions. Design case report forms and related data entry applications. Maintain a thorough understanding of regulatory requirements for data processing operations. Organize and track CRFs, project documents, supplies and enrollments. Participate in project team meetings and recommend processes that lead to timely and successful completion of administrative tasks. | 12/9/2020 |
| 125 | Amarex Germantown, MD Data Administrator I BS in Statistics, Mathmatics, Physical Science, or Equivalent Exp: 0+ Years |
The Data Administrator I is responsible for maintaining and coordinating the production of datasets and acting as a point of contact for questions regarding the data. Other responsibilities: Prepare mapping specifications for interim datasets. Convert interim data to CDISC (SDTM & ADaM). Prepare Tables/Listing Templates for programming. Assists in the quality check of data listings/tables prior to transmission to other groups or inclusion in interim/final reports. Adhere to company procedures related to data handling & data base validation. Maintain a thorough understanding of regulatory requirements for data processing operations. Participate in project team meetings and recommend processes that lead to timely and successful completion of administrative tasks. | 12/9/2020 |
| 126 | Amarex Germantown, MD Proposal Development Associate BS in Scientific or Business Related Field Exp: 0+ Years |
The Proposal Development Associate works as part of the Business Development team by providing support in the development of project proposals, work orders, amendments, and vendor contracts, including budgets for all the preceding. The Associate may participate in sales presentations, client interactions, marketing efforts, and other business development functions. Responsibilities: Support the development of proposals, work orders, and amendments for projects in consultation with Business Development team. Support project budget preparation in consultation with supervisor. Negotiate contracts and budgets with sub-vendors as necessary. Support handoff of new projects to operating team. Maintain client and company experience databases. Provide support to sales and marketing groups as needed. Provide miscellaneous support to the Business Development team as needed. | 12/9/2020 |
| 127 | Amarex Germantown, MD Quality Assurance Assistant BS in Biotechnology Field Exp: 1+ Years |
The Quality Assurance (QA) Assistant provides support to the Quality Assurance department. Responsibilities: Tracking QA project timelines. Assisting with scheduling of internal and external meetings and audits. Preparing and distributing audit/meeting agendas and minutes. Maintenance of employee training files. Maintaining QA department files. Attending training sessions for all departments. Other general administrative support duties as assigned. | 12/9/2020 |
| 128 | Amarex Germantown, MD Safety Coordinator BS in Scientific or Health Related Field Exp: 0+ Years |
The Safety Coordinator will assist in data entry of adverse events, reviewing the data and communications such as query generations in Clinical Trials. Responsibilities: Enter incoming data into related tracking systems and databases. Handle incoming data from clinical trial sites. Follow the company and department SOPs and other regulatory guidelines, if required. Write data summary narratives and reports, as needed. Perform data reconciliation for ad hoc and annual reports. Organize, attend and take minutes of meetings. Provide administrative/logistical support. Other duties, as assigned e.g. assist with coding activities. | 12/9/2020 |
| 129 | Amarex Germantown, MD Safety Data Analyst Graduate Degree in Medical Sciences Exp: 0+ Years |
The Safety Data Analyst processes Adverse Event (AE) and Serious Adverse Event (SAE) cases promptly and with medical accuracy. The Safety Data Analyst will also assist the Supervisor with Medical Coding and Medical Monitoring activities and overseeing the overall conduct of pre- and post-marketing studies with regard to Safety of the subjects. Responsibilities: Develop Clinical Safety, Medical Coding and Medical Monitoring plans. Code medical data including medications (utilizing WhoDrug), adverse events and serious adverse events (utilizing MedDRA). Process, document, and report information on Adverse and Serious Adverse Events to the client and the FDA. Prepare safety narratives. Prepare safety case reports to the FDA and regional regulatory agencies using MedWatch and CIOMS-I forms, and annual/periodic safety reports. | 12/9/2020 |
| 130 | AmbioPharm Augusta, SC Quality Assurance Trainer BS in Biology, Chemistry, or Other Life Science Exp: 1+ Years |
Responsibilities: Provide training to new employees on cGMP concepts, SOPs, Batch Record execution, Batch record reviews, and Investigations. Basic understanding and knowledge of techniques, instrumentation, and lab functions to identify problems and support the completion of work assignments. Review proposed SOP revisions and provide feedback to management. Real-time audit of batch records in the production suites for completeness, documentation, calculation errors and conformance to critical process parameters. Perform room and equipment clearances per procedure following cleaning conducted by production. Data entry to support water, HVAC, and other utilities. Complete additional tasks as assigned by the supervisor. | 12/9/2020 |
| 131 | AmbioPharm Augusta, SC Quality Control Chemist I BS in Chemistry or Life Science Exp: 1-2 Years |
Responsibilities: 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. | 12/9/2020 |
| 132 | Ambry Genetics Aliso Viejo, CA CLS Extraction and Distribution BS in Chemical, Physical, Biological, or Clinical Laboratory Science Exp: 0-4 Years |
The Clinical Laboratory Scientist (CLS) is responsible for following all standard operating procedures of the laboratory and adhering to all quality regulations. Additionally, the technologist may be assigned duties by the Lab Manager, Lab Supervisor, and other Clinical Laboratory Operations Leadership for the advancement or maintenance of the laboratory. Other responsibilities: Follow all procedures and protocols pertaining to patient sample processing, pre-analytical, analytical, and post-analytical testing and general laboratory system that do not directly involve the manipulation of patient samples or products generated from patient samples of assigned assays (typically 1-2 methodologies). Adhere to all Quality regulations (CAP, CLIA & New York State) and ensure all training and competency forms are complete. Daily processing of patient samples within assigned workflow or assay. This includes generating work lists, plate maps, pulling and filing of primers and reagents daily, pulling and filing of patient samples daily and accurately processing of samples within assigned workflow or assay within specified TAT’s. Timely and accurate completion and update of sample processing paperwork and lists on a daily basis either manually or electronically making sure to note any abnormal issues. | 12/9/2020 |
| 133 | Ambry Genetics Aliso Viejo, CA CLS I - Clinical Validations BS in Chemical, Physical, Biological, or Clinical Laboratory Science Exp: 0-2 Years |
The Clinical Laboratory Scientist I (CLS I) is responsible for following all standard operating procedures of the laboratory and adhering to all quality regulations while leading the validation of new assays and process improvements to the clinical laboratory of one to two assigned methodology workflows. Additionally, the technologist may be assigned duties by the Clinical Validations Director Manager, Clinical Validations Supervisor, and Clinical Validations Lead. Other responsibilities: The CLS I, Clinical Validations may be assigned to a specific methodology workflow or no more than two workflows. Validate an existing or newly developed assay or technology per CAP, CLIA and New York (NY) guidelines. Evaluate new in-house and third-party software systems and validate the software. Ensure validation plans and summaries are written per CAP, CLIA and NY requirements alongside developing and /or updating the SOPs appropriately. | 12/9/2020 |
| 134 | Amicus Therapeutics Philadelphia, PA Associate Scientist, Bioanalytical Group MS in Chemistry, Biology, or Related Exp: 0-2 Years |
Amicus is seeking an Associate Scientist to join the Bioanalytical team and perform LC-MS/MS method development and study sample analysis to advance Amicus projects and programs. Responsibilities: Performing routine analysis for the quantification of small-molecule drugs, lipids, biomarkers and peptides in biological samples using defined LC-MS/MS methods. Processing and evaluating analytical data obtained from LC-MS/MS analysis of study samples using appropriate software. Reporting results of the study sample analysis, prepare study associated documentation, and maintain an electronic laboratory notebook. Developing novel LC-MS/MS methods for the quantification and/or characterization of proteins and biomarkers of disease. | 12/9/2020 |
| 135 | Amneal Pharmaceuticals Brookhaven, NY Scientist I, Quality Control BS in Chemistry or Related Exp: 1+ Years |
The Scientist I - QC 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. Other responsibilities: Performs physical and chemical analysis of 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 IR spectroscopy, UV-Vis spectroscopy, and chromatographic techniques adhering to company policies as identified in standard operating procedures (SOPs). Prepares samples for analysis involving thorough cleanliness and complex steps for analysis using chromatographic techniques and other analytical techniques as applicable. | 12/9/2020 |
| 136 | Amneal Pharmaceuticals Brookhaven, NY Scientist II, Quality Control MS in Chemistry or Related 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. Other responsibilities: Performs chemical analysis of 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 IR spectroscopy, UV-Vis spectroscopy, and chromatographic techniques, adhering to company policies as identified in standard operating procedures (SOPs). | 12/9/2020 |
| 137 | Amneal Pharmaceuticals Brookhaven, NY Production Engineer BS/MS in Engineering Discipline Exp: 0-1 Years |
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. Responsibilities: Keeps equipment operational by working with Management to coordinate maintenance and repair services; follows manufacturer's instructions and established procedures; requests special service. Reviews design documents related to procurement of new equipment; perform testing and operation of equipment. Prepare reports, charts, and tables based on established statistical methods to drive process enhancements such as tooling changes and in-process testing controls for management review. Evaluate, improve and validate current manufacturing practices or processes with an effort for continuous improvement towards productivity, quality, reliability and consistency. Assist in the development of manufacturing processes by studying product requirements; researching, designing, modifying, and testing manufacturing methods and equipment; conferring with equipment vendors. | 12/9/2020 |
| 138 | Amneal Pharmaceuticals Branchburg Township , NJ QA Systems (Caliber) Coordinator BS in Relevant Discipline Exp: 1+ Years |
The Quality Systems Coordinator leads and reports data generation, data analysis and data interpretation. Create summary findings to support investigations, Corrective and Preventive Action (CAPAs), complaints etc. Monitors short-term and long-term effectiveness checks and monitors quality assurance trends related to Quality Management System (QMS) processes. Responsibilities: The QA coordinator will work collaboratively with users of quality system software on the collecting and distribution of reports related with quality documents. This includes coordinating and facilitating all aspects of planning, evaluation and reporting, problem resolution and solution to any quality issue. Performs evaluation of Change Controls in accordance with established procedures and ensures close out of these documents. Provides Quality Assurance (QA) management with timely data analysis and insights for potential corrective actions and improvements; and works collaboratively with QMS process owners, QA management and stakeholders to support quality improvement and data collection and organization. | 12/9/2020 |
| 139 | Amneal Pharmaceuticals Brookhaven, NY Validation Engineer I BS in Pharmaceutical Manufacturing, Engineering, Science, or Relevant Field Exp: 1+ 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. Responsibilities: Assist in the preparation/ execution of Installation Qualification (IQ)/Operational Qualification (OQ)/ Performance Qualification (PQ) protocols for equipment, facility and utilities as well as related software. Help generate qualification report and help summarize the results which will be reviewed by the supervisor. Performs re-qualification of equipment, facility and utilities as required under supervision. Identify deviations encountered during IQ/OQ/PQ execution and work with supervisor to implement mitigation solution. Draft Standard Operating Procedure (SOP) for new operational equipment. | 12/9/2020 |
| 140 | Amneal Pharmaceuticals Piscataway, NJ Scientist II, AR&D MS in Chemistry or Related Exp: 1+ Years |
The Scientist-2 is a mid-level analytical scientist opportunity supporting the analytical development of pharmaceutical oral dosage form. The individual in this capacity performs analytical methods qualifications/validations, analyzes active pharmaceutical ingredients, excipients, and finished dosage forms using appropriate analytical methods and maintains/qualifies analytical equipment. Responsibilities: Performs analysis and release of active pharmaceutical ingredients, excipients, in-process materials, and finished drug products to support the formulation development team, maintaining full compliance with all applicable US FDA - cGMP regulations and internal SOPs. Develops and optimizes new and existing analytical methods for qualification and release testing of products. Develops stability indicating methods and performs methods validation. Provides timely responses to all internal and external inquiries. | 12/9/2020 |
| 141 | Amneal Pharmaceuticals Piscataway, NJ Scientist II, Metrology/Quality Control MS in Chemistry or Related 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. Responsibilities: Performs chemical analysis of 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 IR spectroscopy, UV-Vis spectroscopy, and chromatographic techniques, adhering to company policies as identified in standard operating procedures (SOPs). Prepares samples for analysis involving thorough cleanliness and complex steps for analysis using chromatographic techniques and analyzes. Creates and maintains laboratory record documentation (notebooks and computer-based), documents exact steps followed during analysis execution, calculates and reports results in a timely manner. | 12/9/2020 |
| 142 | Amunix San Francisco, CA Lab Technicnan BS in Chemistry, Biology, or Related Exp: 1-2 Years |
The Lab Tech is responsible for supporting routine operations of the Fermentation and Purification Labs and completing routine laboratory procedures under the direction of the BioProcess Development and Manufacturing Lead. Other responsibilities: Conduct routine lab procedures (preparation of media and solutions, calibration of and testing with pH and conductivity probes, endotoxin testing, and good record keeping throughout). Weigh and mix specified components in calculated amounts, recording throughout. Set up and operate necessary equipment to support the above. Collaborate with manager, team members, and other functional groups at Amunix to plan, prioritize, and meet delivery deadlines. | 12/9/2020 |
| 143 | A2 Biotherapeutics Los Angeles, CA Research Associate MS in Scientific Discipline Exp: 1+ Years |
The Therapeutic Technology team is seeking a highly motivated individual with experience in biochemistry, cell and molecular biology and assay development. The successful candidate will join us at our research facility in Agoura Hills, CA and work on cutting edge science in a dynamic, fast-paced and team-oriented environment. Responsibilities: The design, execution, documentation and presentation of biochemical and cell-based experiments. Development and implementation of novel assay protocol. Work with other scientists to design and perform cutting-edge immuno-oncology related experiments that integrate molecular biology, cell culture and assay techniques to develop treatments for multiple types of solid tumors. Collaborate with team members to select, profile and advance clinical candidates in a scientifically rigorous manner. Work under supervisor’s guidance both independently and collaboratively to implement novel laboratory processes and solve technical problems. | 12/1/2020 |
| 144 | Abbott Irving, TX PCB Layout Engineer Preferred BS in Electrical or Mechanical Engineering, Material Science, or Related Exp: 6+ Months |
The PCB Layout Engineer will be working within a team environment to design and draft complex electronic PCB’s layouts and drawings. The qualified individual must be able to work in a fast-paced team environment and be responsible for schedules and deadlines. Responsibilities: Create footprints per supplier datasheets and IPC standards. Maintain and support Abbott eCAD Library. Layout of complex mixed-signal, mixed technology, high-density PCB designs. Provide full documentation for fabrication and assembly. Understanding pin mapping assignments in complex part symbols. Layout for placement and circuitry routing of PCBs for optimal electrical, EMI, thermal, and structural performance. Understanding of design rules constraint management and parasitic analysis. Use 3rd party tools to perform Design Rule Checks and insertion of test probes. Interface with Vendors and Suppliers to import and export data for fabrication of bare boards and installation of electronic and mechanical components. | 12/1/2020 |
| 145 | Abbott Des Plaines, IL Scientist - Spectroscopy Lead (AMD) MS in Biophysics, Biochemistry, Physics or Biomedical Engineering ` Exp: N/A |
Abbott Molecular has an opening in its Des Plaines, IL site for a Scientist- Spectroscopy Lead who would conduct research for on-market product utilizing multiple experimental techniques. Responsibilities: Investigates and develops new procedures under the guidance of a research lead. Interacts with other groups and shares information; participates in team activities. Summarizes data and analyzes results, independently formulates conclusions, and determines future experiments. Actively participates in routine maintenance, lab safety; may assume roles of responsibility, such as training or document control. Prepares and delivers presentations of project results to others; presents data to larger and more diverse audiences. Teaches processes and problem-solving techniques. May lead others in project teams. | 12/1/2020 |
| 146 | Abbott Abbott Park, IL Research Scientist BS in Chemistry, Biochemistry, Chemical Engineering, Biology, or Medical Technology Exp: 1+ Years |
Abbott Diagnostics has an opening for a Research Scientist. This qualified and motivated scientist will join a dynamic R&D team developing novel methodologies and assays for next generation diagnostic applications. These activities may also support the development of next generation instrumentation. This individual will help conceive, plan, design, and conduct advanced studies. The Research Scientist will investigate and develop new procedures. He or she will act as an independent contributor and will interact/coordinate with other groups and functions on project development and improvement. The successful candidate must have strong analytical and quantitative skills, as well as excellent oral and written communication skills. | 12/1/2020 |
| 147 | Abbott Irving, TX Systems Engineer - Predictive Analytics BS in Electrical, Mechanical, Computer Science, or Systems Engineering or Related Exp: 1+ Years |
The Systems Engineer is responsible for understanding the integrated set of standards, sub-standards, and assemblies needed to design and manage systems over their life cycles. 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. This includes a multitude of systems requirements that range from design, development, test methodologies, validations, risk analysis, documentation, and process improvements. | 12/1/2020 |
| 148 | Abbott Abbott Park, IL Sr. Process Scientist - Fermentation MS in Chemical Engineering, Chemistry, Biology, or Biochemistry Exp: 1-5 Years |
The scientist will lead and consult on multiple complex projects defined for process investigations; design changes; resolving production issues and improving product availability and profitability. Leads a cross functional team with the required product/process knowledge to assess impact and develop plan. Focus will be in protein purification with one or more of fermentation, cell culture or recombinant protein experience. Other responsibilities: Demonstrate an understanding of the application of the Quality Policy through daily activities. Maintain vigilance to ensure adherence to the Quality Policy and system procedures by promptly reporting noncompliance issues to management. Develop and apply operations and process knowledge to area of support. Use sound judgment; appropriate scientific methods and thorough data analysis. Conceive; plan; design; execute; and document projects/activities efficiently and in conformance with applicable OPs. | 12/1/2020 |
| 149 | Abbott Columbus, OH Analytical Assistant Chemist BS in Chemistry, Biology, or Closely Related Technical Field Exp: N/A |
Responsibilities: Conduct raw ingredient analyses which consist of simple titrations, moisture testing, organoleptic testing, sediment testing, etc. Conduct in-process and finished product testing including: determination for vitamins using various lab methods, protein and mineral analysis; fat by Mojonnier extraction technique, total solids determination, Iodide, chloride testing, and fatty acid profiles by Gas Chromatography per approved Laboratory Methods. Complete appropriate documentation and calculations needed for Standardization tests including: KOH, vitamin additions, final water calculations and physical tests such as pH, viscosity, grain color, and sensory evaluation. Complete housekeeping responsibilities such as washing glassware, waste disposal, general laboratory sanitation, etc. | 12/1/2020 |
| 150 | Abbott Tampa, Fl Clinical Specialist I - CPT BS in Scientific/Technical Field Exp: 1-2 Years |
As a member of the clinical support team, you'll be responsible for providing technical clinical expertise and support of the sales process to colleagues, current customers and/or potential customers. Other responsibilities: Works under general direction with clinical and sales teammates to identify and capitalize on sales opportunities by creating competency, comfort and expertise with all Abbott Chronic Pain Therapies among physicians, support staff and customers within assigned geography. Performs work that involves a high degree of independence. Exercises independent judgment in planning, organizing, and performing work. Seeks to continually improve territory efficiency. Will begin to conduct PCP work and educational in services, as directed. Provides medical professionals with sales support, information, and training on the use of Company products and with staff education, in-services and technical troubleshooting. | 12/1/2020 |
| 151 | AbbVie San Francisco, CA Associate Scientist II, In-Vivo Pharmacology MS in Relevant Field Exp: 0+ Years |
AbbVie is looking for an Associate Scientist II/Scientist I with experience in in vivo pharmacology study execution in various mouse models of cancer. The main role will involve conducting in vivo research studies from start to finish including tumor implantation, data collection, and data analyses. Additional opportunities to learn new skills and to work on ex vivo lab experiments will be provided as smaller roles, and based on project need and candidate’s interest. Above all, they are looking for a highly motivated and collaborative individual with a passion for oncology research, who enjoys working in a fast-paced and highly dynamic working environment. | 12/1/2020 |
| 152 | AbbVie Branchburg, NJ Quality Control Technician II BS in Relevant Field Exp: 1-2 Years |
The Quality Control Technician II will be responsible for, but not limited to, performing inspections following procedures, specifications and applicable standards and regulations. Providing technical support to cross-functional teams as needed, identifies potential discrepancies and nonconformance and alert management. Performing porcine and human tissue receipt, and inspection, in-process inspections i.e. e-beam), and performing product discard as per procedures in an electronic data system. Ensuring proper equipment functionality and appropriate levels of supplies. Supporting and partnering with cross-functional teams to resolve any issues or non-conformance encountered. Assisting in documentation updates and related change controls activities as needed. Perform ing applicable actions for Nonconformance Reports (NCRs), Supplier Issues (SIs), Engineering Change Orders (ECOs), etc. | 12/1/2020 |
| 153 | AbbVie Lake County, IL Associate Scientist II/Scientist I, Process Chemistry MS in Chemistry Exp: 0-2 Years |
AbbVie Process R&D is seeking a Chemist with strong synthetic skills. This individual will work under the mentorship of a supervisor to discover, develop, and execute routes to compounds that treat a variety of diseases. The candidate will be a member of an integrated Process Research & Development project team consisting of chemists (synthetic, structural, analytical) and engineers with the goal of identifying and developing novel and practical routes to newly discovered therapeutic targets. The ideal candidate will be enthusiastic and productive, with excellent communication skills and strong functional expertise in synthetic organic chemistry, compound synthesis, and characterization. Responsibilities: Independently design and conduct critical experiments that further project goals. Implement and may innovate new experimental protocols/techniques. Understand the goal and maintain a high proficiency in his/her projects as well as the overall program. Interpret results and draw conclusions from own multistage experiments, note significant deviations, then suggest, design, and pursue relevant experiments. | 12/1/2020 |
| 154 | AbbVie Irvine, CA Scientific Associate BS in Chemistry, Biology, or Related Exp: 1-3 Years |
The candidate will have a critical role in supporting the overall Aesthetics Biological Research Program by managing inventory, administration of personnel training, and management of personnel security access. He/she will be the team Subject Matter Expert regarding a custom inventory database as well as policies and procedures for registration, use, shipment, and receipt of inventory. The candidate will coordinate and oversee inventory audits and will represent the team in interactions with EH&S and both internal and external auditing agencies. The candidate will identify and recommend changes in policies, procedures, and software design. He/She will coordinate shipment and receipt of samples, including entry of inventory into the electronic inventory system. Responsibilities will also include management of a freezer monitoring system. The candidate will also utilize a learning management system to administer and track personnel training on required SOPs. He/She will complete, submit, and manage security access requests for secured lab areas. In addition to the Biologic inventory responsibilities, the candidate will also support the team with protein quantification, SDS-PAGE, Western blot, and additional protein and DNA analysis, including documentation of results. Candidate will also partner with Departmental Lab Operations staff to escort vendors and service technicians during on-site visits into research labs. | 12/1/2020 |
| 155 | AbbVie Lake County, IL Associate Scientist II/Scientist I, Toxicology Study MS in Scientific Discipline Exp: 0-2 Years |
This position sits within the Preclinical Safety group at AbbVie and reports to a senior manager in Toxicology. The Associate Scientist II / Scientist I, Toxicology Study Coordinator aides in the planning, conduct and reporting of non-GLP and GLP toxicology studies, acting to support the Study Director and regulatory infrastructure. Responsibilities: Draft study plans, amendments, and report components. Assist in the technical conduct of nonclinical studies including account set-up in electronic data capture system and scheduling of study events. Perform data review periodically through study conduct and at study completion. Facilitate communications among study personnel. Coordinate the archival of study data and specimens. Support GLP infrastructure through quality control responsibilities and active participation in process improvement activities. | 12/1/2020 |
| 156 | AbbVie Lake County, IL Senior Safety Data Scientist MS in Health Sciences Field Exp: 1-2 Years |
This position partners with cross functional stakeholders in support of the product safety profile and benefit risk throughout product lifecycle through signal detection, signal evaluation, and preparation of written and verbal summaries of signal management activities and risks to patient safety to present to senior management and regulatory authorities globally. Responsibilities: Collaborates with safety and clinical teams to develop strategies and approaches for signal assessments and regulatory requests by analyzing data from multiple sources. Analyzes data to support signal assessment and contributes to ad hoc regulatory safety requests using data from multiple sources with supervision. Utilizes medical judgment to determine the impact of identified safety issues on the compound/ product’s benefit-risk profile. Communicates findings of surveillance activities and safety assessments to product teams and leadership to inform on necessary risk minimization activities, including label changes. Responsible for standard surveillance activities for a product’s life cycle (one or more assigned compounds and products) through review of safety data from clinical trials, safety databases, and the literature. | 12/1/2020 |
| 157 | AbbVie Lake County, IL Combination Product Test Engineer MS or ME Exp: 0-5 Years |
Responsibilities: Execute test procedures and protocols supporting engineering testing and verification testing, analyze data, document in lab notebooks, and present results to cross-functional teams. Experience using Zwick and flow measurement equipment is preferred. Familiarity with 3D printing, CT Scanners, Viscometers, Climate Chambers, etc. is a plus. Define, develop, and validate test methods. Create verification plans, protocols, records, and reports. Support investigations and issue resolutions. Familiarity with DHR tools such as LinkUS, or Cockpit is desired. Experience with Solidworks, Minitab, Engineering Lab Notebook (ELN) is a plus. Expected to recommend improvements in design, processes, execution of a project or task as well as the maintenance of a program. Work in an independent manner under the guidance of a supervisor or technical lead. Assignments have clear and specified objectives. Complies with applicable policies and procedures, regulatory and safety requirements. | 12/1/2020 |
| 158 | Abeona Therapeutics Cleveland, OH Associate, Process Development MS in Scientific Discipline Exp: 1-2 Years |
Abeona is looking for an Upstream Process Development Associate to join their team in Cleveland, OH. The successful candidate will be responsible for to support upstream process development initiatives and will be an integral part of a fast-paced group responsible for developing production processes for the manufacture of clinical AAV gene therapies. Responsibilities will include executing experiments across multiple scales from small shake flask cultures up to 200 L bioreactors. The ideal candidate will have some experience in production of biologics in either a research or development setting. Conducting research involving biochemical assays, effectively communicating results through high quality technical reports and oral presentations, and collaboration with your team is an integral part of this position. | 12/2/2020 |
| 159 | AbSci Vancouver, WA Research Associate I/II Analytical Development and Purification BS in Analytical Chemistry, Biochemistry, Molecular Biology, Bioengineering or Related Exp: 1-2 Years |
The Research Associate I/II will play a significant role in analytical method development and characterization of therapeutic proteins expressed using SoluPro™, AbSci’s proprietary E. coli expression platform. Assays include, but are not limited to, protein concentration by A280, SDS-PAGE, Western blot, LC (e.g. LC-UV, SEC, IEX, etc.), CE-SDS, and/or LC-MS (e.g. intact mass, peptide mapping). Responsibilities: Independently perform laboratory tasks for the analysis of complex therapeutic proteins in lysates by a variety of different techniques, including SDS-PAGE, Western Blot, tip-based immunoassays, LC-UV, automated liquid handlers, MS, protein concentration, etc. Operation of sophisticated chromatography instrumentation, (e.g. automated liquid handlers, AKTAs, and HPLCs). Preparation of buffers, reagents, and other sample preparation techniques to support sample analyses. Operation of sophisticated chromatography instrumentation, (e.g. HPLC, MS, CE, etc.). | 12/2/2020 |
| 160 | AbSci Vancouver, WA Research Associate , High-throughput Screening BS in Microbiology, Biochemistry, or Related Exp: 1-2 Years |
The Research Associate will be primarily occupied with executing a variety of high throughput assays. These include flow cytometry and cell sorting, ELISA, and plate based micro-fermentations. This position will be responsible for independently preparing media and buffers, processing samples, and preliminary analysis of results. Work will be done on a variety of automated hardware platforms including flow cytometers and liquid handlers. Candidate is enthusiastic about laboratory bench work, exhibits meticulous attention to detail, an eagerness to learn new techniques, and is comfortable working in a highly dynamic and rapidly scaling company. Responsibilities: Prepare needed buffers, stock solutions, and media. Independently execute strain screening experiments. Compile and enter data into the company’s LIMS system. Preliminary analysis of data to ensure operational integrity before handoffs to downstream groups. | 12/2/2020 |
| 161 | AbSci Vancouver, WA Research Associate/Sr. Research Associate - Cloning MS in Molecular Biology, Biochemistry, Microbiology, or Related Exp: 1-2 Years |
The Research Associate/Sr. Research Associate, under direction of the Molecular Sciences team, will support innovative experimental research that advances AbSci’s proprietary E. coli SoluPro® expression platform. Primary responsibilities include providing core support to ongoing DNA construction, strain engineering, and NGS sequencing activities. The ideal candidate will demonstrate rapid mastery of assigned tasks and the capacity to take on additional technical responsibilities within an expanding team. | 12/2/2020 |
| 162 | Absorption Systems Exton, PA Associate Scientist - Analytical Chemistry BS in Chemistry, Biochemistry, or Equivalent Exp: 0-2 Years |
As an Associate Scientist in the Analytical Chemistry Screening Department, you will work in a fast-paced environment with a team dedicated to helping our Sponsors select drug candidates to move forward in their pipelines. You will run various in-vitro screening assays related to helping understand how potential drugs overcome the biological barriers involved in getting to their ultimate target. You will work hands on with the latest technology in LC and MS systems to rapidly and efficiently analyze samples from these assays and provide our Sponsors the results they need in the time they need them. You will also prepare study protocols, analyze the data resulting from our various experiments, and prepare study reports to communicate those results to our Sponsors. | 12/2/2020 |
| 163 | Absorption Systems Exton, PA Associate Scientist/Scientist - Molecular Biology (PCR and Cell Biology) BS or Higher in Molecular Biology Exp: 0-2 Years |
Skills: Knowledge and experience conducting experiments in some or all of the following areas (priority for more experience in PCR and cell biology): Cells culture and transduction/transfection in cells, extraction of DNA/RNA from cells and tissues, assays of transfection/transduction efficiency, and RT-qPCR and qPCR. Responsibilities: Preparation of assay protocol, planning and conducting of experiments under the direction of a senior scientist. Designing new PCR methods. Conducting molecular biology assays, such as RTqPCR and qPCR. Preparing and maintaining cell cultures and reagents. Transfection and transduction in cells. Documenting all results in laboratory notebooks. Writing reports for the study project under the direction of supervisor. | 12/2/2020 |
| 164 | Absorption Systems Medford, MA QC Associate Minimum of BS in Biology, Chemistry, Pharmacology or Related Exp: 1-3 Years |
The QC Associate will work in a cGxP compliant Laboratory to support quality control of Bioanalytical and Bioassay Assay Validation and Sample Analysis. Responsibilities: Sample management including receipt, accessioning, logging, and storage. Critical reagent and supply management including receipt, inspection, and release for use. Review of Standard Operating Procedures (SOPs), Validation and Sample Analysis Reports, and individual data to assure the highest quality. Developing Word and Excel templates to improve and expedite data analysis and report writing. Reviewing logbooks for completeness and accuracy. Preparing data for archiving. Interacting with Principal Investigators, Scientists, QAU, and Management. | 12/2/2020 |
| 165 | Absorption Systems San Diego, CA Research Associate BS in Pharmaceutical Sciences, Life Sciences, or Pharmacology Exp: 1-3 Years |
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. Prior experience working with other in vivo models may be considered even if there is no direct experience working with medical devices, stem cells or ophthalmology. Responsibilities: Participate in study design and preparation of preclinical studies. Fully support execution of preclinical studies. Help in the preparation of study protocols and reports. May be required to serve on the Institutional Animal Care and Use Committee (IACUC). Interface with different teams including in vivo scientists, QC/QA, Account Managers/Sales. Maintain accurate records in various internal databases. | 12/2/2020 |
| 166 | Absorption Systems San Diego, CA Research Associate, Formulations BS in Relevant Field Exp: 1-3 Years |
Responsibilities: Perform preparation of test article/substance dosage solution/suspension(s), ensure preparation procedures and calculations are standardized, performed consistently and recorded correctly by the technical personnel. Receive all incoming test articles/substances and reagents. Ensure that the documentation for the use of all test articles/substances and vehicles/reagents to ensure consistency and correctness. Sampling and the shipment of formulation samples. Maintaining cleanliness and general appearance of the Formulations Laboratory. Ensure that test article/substance(s) from completed studies are returned to the sponsor as needed. Responds to Quality Assurance audits of preparation procedures and calculations. Maintaining an up to date inventory of reagents, test article/substance, vehicles and samples. Review chemistry data for submission at completion of study. Prepare accurate packing list for the shipment of test article/substances and samples to the sponsor and/or analytical laboratory. Notify appropriate personnel of shipments. | 12/2/2020 |
| 167 | Absorption Systems Exton, PA Scientific Account Manager - Drug Development MS in Pharmaceutical Sciences, Life Sciences, or Pharmacology Exp: 0-1 Year |
Absorption Systems, a preclinical Contract Research Organization located in Exton, Pennsylvania, is seeking a candidate for a Scientific Account Manager position. Scientific Account Managers (SAMs) are key members of the Absorption Systems Sales Team and function as liaisons between sponsors, internal research scientists, study directors, and business development team members. AMs use their knowledge of preclinical drug testing to design and manage studies for a wide range of sponsor requests ranging from lead optimization through regulatory submissions. Responsibilities: Design studies that meet sponsors' needs in a scientifically sound and cost effective manner. Address customer requests for information promptly and accurately. Follow internal processes for accurate record keeping of study designs, proposals, and pricing logic. Rapidly increase knowledge of preclinical drug testing to enable peer-interactions with clients. | 12/2/2020 |
| 168 | Absorption Systems Exton, PA Scientist/Sr. Scientist - Molecular Biology MS in Molecular Biology, Biochemistry, Microbiology, or Related Exp: 0-2 Years |
Responsibilities: Preparation for protocol of assay, planning and conducting experiments under the direction of a senior scientist. New PCR design. Conducting studies on molecular biology assays, such as RT-qPCR and qPCR. Preparing and maintaining cell cultures and reagents. Transfection and transduction in cells. Documenting all results in laboratory notebooks and presenting research data in group and other meetings. Project study report writing under the direction of supervisor. Cell culture and transduction/transfection in cells. Extract DNA/RNA from cells and tissues. Perform assays of transfection / transduction efficiency. RT-qPCR and qPCR. | 12/2/2020 |
| 169 | Associates of Cape Cod Falmouth, MA Quality Control Analyst I BS in 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. | 12/2/2020 |
| 170 | AccuraGen Menlo Park, CA Research Associate/Senior Research Associate BS/MS in Biology or Related Exp: 1+ Years |
AccuraGen is looking for a highly motivated research associate to join their Assay Development team. The assay development team is developing a library preparation platform that will provide the most diverse analysis of multiple analytes in plasma. It will deliver unparalleled accuracy of cancer detection from a minimal amount of patient blood samples. Responsibilities: Plan, execute and interpret experiments. Analyze data, evaluate results, form conclusions, and recommend future experiments. Ensure accurate and consistent recording of experiment methods, materials and results; keep a high-quality laboratory notebook. Communicate and work efficiently with other groups within R&D team. Adjust work schedule to meet time-sensitive project milestones. | 12/2/2020 |
| 171 | AccuraGen Menlo Park, CA Scientist I, Research and Development MS in Molecular Biology Exp: 1+ Years |
AccuraGen is developing systems that will provide the most sensitive, accurate, and robust NGS-based ctDNA mutation detection. It will deliver unparalleled accuracy from a minimal amount of patient blood samples. They are looking for an outstanding individual to join their R&D team to drive technology innovation, product development and commercialization. Responsibilities: Plan, design and execute assay research and development experiments. Analyze data, evaluate results, form conclusions, and provide and/or implement improvements. Communicate results with colleagues and R&D management. Ensure product performance by utilizing proven development practices and/or developing novel procedures to overcome obstacles. Optimize and document SOPs to achieve commercial levels of stability, robustness and performance. | 12/2/2020 |
| 172 | Acellapharma Alpharetta, GA Customer Complaint Quality Coordinator BS in Scientific Discipline Exp: 1-3 Years |
The customer complaint quality coordinator will be the first point of quality contact for Acella and Avion complaints and ensure that complaints are managed in accordance with site SOP and regulatory guidance. Responsibilities: Record and monitor consumer complaints in a validated document management system. Triage and initiate investigation requests with both internal team and external suppliers. Provide a written response to the consumer/customer stating the outcome of the investigation along with the pharmacovigilance guidance as needed. Work and assist medical advisors as needed. Generate a MedWatch report as a result of a serious adverse event. Respond to technical queries related to the products. Assist the Drug Safety management or delegates as required. Work with pharmacovigilance service providers as required. | 12/2/2020 |
| 173 | PharmaSeek LLC Cary, NC or Madison, WI, Clinical Research Analyst BS/MS in Scientific or Mathmatic Discipline Exp: N/A |
The Clinical Research Analyst is responsible for assisting research institutions with budget development and negotiation, coverage analysis, and clinical trial management system services. The Clinical Research Analyst will complete these critical functions in a manner designed to expedite the conclusion of the start-up process for our clients while maintaining a high level of quality. They are in need of critical thinkers to help interpret Medicare/Medicaid guidelines, analyze clinical research protocols, and work directly with our clients to develop and negotiate clinical trial budgets. Responsibilities: Interpret Medicare/Medicaid coverage decisions and national guidelines to determine what procedures are billed to the sponsor and which are billed to Medicare/private insurance. Identify appropriate research modifiers to be placed on claims. Develop and negotiate clinical trial budgets based on client’s preferred pricing methodologies. Build studies within client’s clinical trial management system (CTMS). Work with Senior Clinical Research Analysts and Manager to review and alter deliverables as needed. | 12/2/2020 |
| 174 | KMR Group INC Chicago, IL Data Analyst BS in Engineering, Mathmatics, or Sciences Exp: 1-3 Years |
The Data Analyst plays a critical role and is responsible for turning data into information, information into insight, and insight into business decisions. The primary responsibilities include data analysis, data management, data operations, and application validation. Other responsibilities: Manage raw data, query, and create databases using Excel. Construct data frameworks for analyzing data; analyze data using standard methods as well as statistical methods, interpret results, and present clear summaries. Visualize data using Excel and Visio. Interpret data analysis and write reports. Assist in the development and delivery of data analysis packages for client data services. | 12/2/2020 |
| 175 | Acumed Hillsboro, OR Product Engineer 1, Sustaining (Medical Device) BS in Mechanical or Bio-Mechanical Engineering, or Equivalent Exp: N/A |
The Product Engineer, Sustaining is responsible for products after development is completed and when they are released for commercialization. This includes supporting manufacturing, quality improvements, product analysis on field complaints, document Remediation, biocompatibility of raw materials and final products, additional testing required by regulatory bodies for follow on regions and supporting product training to surgeons as needed. When needed, the Product Sustaining Engineer also participates on new product development teams and/or product update and extension projects. All of these efforts involve research, planning, idea creation and realization, concept development, specification generation, testing and validation protocols, as well as effective communication with team members, management, and customers. | 12/2/2020 |
| 176 | Adaptimmune Philadelphia, PA Quality Control Associate BS in Relevant Field Exp: 1-3 Years |
The Quality Control Associate will be responsible for conducting in-process and finished product testing associated with Adaptimmune clinical trial material. In addition, the role will be working with other departments for deviations and method transfers. Responsibilities: In-process, finished product and stability testing of clinical trial material. Maintenance of Quality Control Protocols, SOP’s and Test Methods. Deviations, change controls, CAPAs. Method / Technology Transfer of existing methods into the Adaptimmune QC Lab | 12/2/2020 |
| 177 | Adaptive Biotechnologies San Francisco, CA Research Associate II MS in Cell Biology, Immunology, Genetics, Biochemistry, Bioengineering, or Molecular Biology Exp: N/A |
Adaptive Biotechnologies is currently recruiting a Research Associate II to join their TCR Discovery team. The successful candidate will work as a part of a team using cellular assays to screen, characterize and develop T cell receptors as potential therapeutic agents. Responsibilities: Isolate and culture human primary immune cells and cell lines. Transfect mammalian cells, as well as optimize and troubleshoot transfection protocols. Use flow cytometric assays to characterize the specificity and potency of T cell receptors, and assess their potential utility as anti-tumor (or alternative disease) therapies. Take initiative in improving current assays to streamline processes. Assist with pre-clinical studies, using GLP techniques and documentation. Assist in the design and development of new cell based assays as the need arises. | 12/2/2020 |
| 178 | Adaptive Biotechnologies Seattle, WA Accessioning Specialist II BS in Biology or Related Exp: 1+ Years |
The Accessioning Specialist II position will join the Biological Sample Management (BSM) group at Adaptive Biotechnology’s Seattle laboratory. The primary function of this role is to support sample management and chain of custody for Adaptive’s immunosequencing services that includes research, clinical projects, and diagnostic testing. Responsibilities: Enter, upload and ensure accuracy and completeness of information pertaining to samples and related projects through multiple systems. Ensure there is a record of every system transaction relating to each managed sample in order to evidence sample Chain of Custody (COC). Ensure appropriate inventory management (freezer management) of each physical sample through the entire sample management lifecycle. | 12/2/2020 |
| 179 | Adaptive Biotechnologies Seattle, WA Clinical Laboratory Technologist I - PCR BS/MS in Chemical, Physical, or Biological Science Exp: 1+ Years |
The Clinical Laboratory Technologist 1 position will be responsible for processing medically relevant biological samples through extraction or high throughput DNA sequencing assays. This role will work within a team of Laboratorians in a fast-paced, high production setting to process research and clinical diagnostic samples to provide a test result to patients, oncologists and other medical practitioners and researchers. As such, high attention to detail and clinical mindedness are crucial to success in this role. Responsibilities: Assignment to one of two labs performing either DNA extractions from human biological samples, or PCR amplification and high-throughput sequencing assays on DNA libraries. Demonstrate good clinical judgment and integrity. Perform DNA extractions, PCR amplification or high-throughput sequencing assays on DNA libraries. Perform protocols under compliance with regulatory agencies; model appropriate clinical, regulatory and safety practices. | 12/2/2020 |
| 180 | Adaptive Biotechnologies Seattle, WA Principal Quality and Regulatory Affairs Engineer BS/MS in Relevant Scientific Discipline Exp: 1+ Years |
This position is responsible for developing software processes to ensure that software development practices comply with applicable regulatory requirements, as well as supporting day to day quality operations and processes supporting software engineering efforts at Adaptive. This position is accountable for ensuring that the Adaptive SDLC is both efficient as well as compliant with applicable international (IVDD/IVDR), Federal (21CFR), and other applicable regulations. In addition, this position is responsible for maintaining quality processes such as assisting in Nonconformance and CA/PA investigations and actions. The position requires the ability to manage priorities from multiple projects and tasks utilizing effective written and oral communication skills. Will apply quality and regulatory systems knowledge, problem solving and judgment skills to ensure the appropriate balance of quality, compliance and business needs. | 12/2/2020 |
| 181 | ADIMAB Lebanon, NH Research Associate - Antibody Sciences BS/MS in Molecular Biology, Biological Engineering, Cellular Biology, or Related Exp: 1+ Years |
The Research Associate will work in a small team to isolate and characterize antiviral antibodies from primary human B cells for research studies and therapeutic development. The Research Associate will also work on technology development projects to improve Adimab’s antibody discovery pipeline. Responsibilities: Basic handling and culture of yeast and mammalian cells. Primary B cell isolation using fluorescence activated cell sorting (FACS). Single-cell RT-PCR. Quantification of antibody responses via ELISA. Construction and selection of yeast antibody libraries. Mammalian cell based characterization assays. Collection, organization, analysis, and presentation of data. Tracking and upkeep of lab reagents and stocks. Facilitate collaborations with internal and external colleagues. | 12/2/2020 |
| 182 | ADMA Biologics Boca Raton, FL QA Specialist I - Product Release BS in Relevant Field Exp: 1-2 Years |
Responsibilities: Understand the cGMPs and processes such as Quality Systems (e.g., Deviations, Corrective and Preventive Action reports {CAPAs}, Change Controls, and Out of Specifications {OOSs}). Ensure cGMP and regulatory compliance as defined in government regulations such as 21 CFR Parts 11, 210, 211, and 600, as well as compliance with corporate policies and procedures. Review and release manufacturing batch records, and any additional supporting documents including but not limited to logs, charts, specifications, and environmental and WFI data. Perform usage decisions for batch release in SAP. Work with IgG Manufacturing floor personnel and other technical operation departments to resolve documentation and compliance issues. Perform period follow-up of ongoing deviations to assure timely closure of documentation and batch release. Review and approve Certificates of Analysis for batch release in LIMS. Review SOPs and documents from other departments and provide feedback as necessary. Perform review and release of Plasma pools when required. | 12/2/2020 |
| 183 | Trevigen Minneapolis, MN Advanced Quality Technician Minimum of Associates Degree Exp: 1-3 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, equipment operation, inventory, participation in complaint investigations and calibrating equipment. This position will participate in the continuous improvement of our products and customer-centered culture. The technician will also: conduct inspections of raw materials, intermediates and finished goods to ensure specifications and quality standards are met with minimal instruction and supervision, conduct inspection of product literature and labels to ensure accuracy, pay much attention to detail, reconcile documents, compile, analyze and report on data of moderate complexity, and consistently advocate for Quality Ideals by demonstrating commitment to meeting quality requirements in daily work | 11/18/2020 |
| 184 | Trevigen Minneapolis, MN Advanced Research Associate Masters Degree Exp: Up to 2 Years |
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. Participate in troubleshooting as needed. Responsibilities: perform routine bioassays following the instructions for quality control on proteins, antibodies, and related products, perform more complex bioassays following the instructions for quality control on proteins, antibodies, and related products, analyze and report data with the consideration of intra and inter-assay variations and other factors which may affect the assay results, keep accurate records of all experiments performed, follow GMP guidelines, documentation, and workflow, maintain cell lines; isolate primary cells from human/animal blood and animal tissue for use in bioassays, freeze cell stock for future applications. | 11/18/2020 |
| 185 | Trevigen Devens, MA Manufacturing Technician - Filling (INTERNSHIP) Bachelors Degree Exp: 0+ Years |
The Manufacturing Technician is responsible to operate manufacturing equipment and complete all documentation according to cGMP/ISO standards. Provide written documentation of required data throughout the manufacturing operations in accordance to established SOPs, Work Instructions and cGMPs/ISO standards. Provide hands on assistance as needed on equipment lines and manual pack lines. They will also need to understand and follow appropriate standard operating procedures and work instructions such as the regulatory awareness of chemical handling and hazards, labeling, safety procedures, department specific SOP’s, and proper use and basic equipment maintenance. | 11/18/2020 |
| 186 | Trevigen Newark, CA Research Associate, R&D BS in Molecular Bio, Biochem, Cell Bio, or Related Exp: 1+ Years |
The research associate will work within a highly dynamic group and be responsible for developing new products and applications for RNAscope technology. Responsibilities: Execute RNAscope/BaseScope-based assays to support new product development and assay optimization, including but not limited to BaseScope manual assay testing, R&D collaboration projects and RUO raw material improvement projects. Support manufacturing QC for commercial product testing, release and troubleshooting when needed. Facilitate SOP/SPK/SPJ drafting/assay QC procedure transfer from R&D to QC team. Participate in R&D/QC communication and hands-on training. Responsible for experimental design, assay running, data collection and interpretation. | 11/18/2020 |
| 187 | Trevigen Wallingford, CT Bioinformatics Scientist MS in Bioinformatics, Computer Science, Engineering, or Related Exp: 1-3 Years |
They are currently looking for a Bioinformatics Scientist in a multi-role as data analyst, developer, and bioinformatics scientist to support the Simple Plex BU. Experience or coursework with biological sourced data analyzed using various techniques including statistical analysis, machine learning, and data visualization are required. They are looking for a motivated, cross-disciplinary individual to implement novel approaches in data analytics for the purposes of delivering actionable intelligence for assay development, manufacturing, QC, product support, and engineering. Responsibilities: Assist with exploratory analysis of Simple Plex assay data from QC, product support, and R&D projects. Work with biologists, engineering, and product support, to create visualizations and analysis. Drive informed decision making for product development, QC, operations. Establish code and data control process to enable multi-user collaboration across functional areas | 11/18/2020 |
| 188 | Trevigen Cambridge, MA Research Associate (Protein Purification) BS in Related Field Exp: Up to 3 Years |
They are seeking a protein biochemist who will contribute to the ongoing research and development of products including complex assay systems, post-translationally modified proteins and peptides, and recombinant enzymes. The candidate will have previously purified proteins from bacterial, insect, and/or mammalian expression systems, and will have theoretical knowledge or hands-on experience with isolation of proteins from prokaryotic and eukaryotic organisms. Responsibilities: carry out troubleshooting activities under supervision, collaborate with other departments/labs as needed, follow guidelines and comply with all company safety, quality, and training procedures and regulations. | 11/18/2020 |
| 189 | Trevigen San Marcos, CA QC Specialist BS in Biological Science, Chemistry, or Related Exp: 1-5 Years |
Responsibilities: 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. Coordinate, perform and maintain QC testing and scheduling for Stability program. Assist in establishing QC specifications. Assist in the validation testing of equipment and processes. Assist in the review and creation of ISO/QSR documentation. Perform QC assay testing for release of final product. Perform assay testing for Value Assignment, complaints and date extensions. | 11/18/2020 |
| 190 | Trevigen Newark, CA Research Associate, R&D BS in Molecular Bio, Biochem, Cell Bio, or Related Exp: 1+ Years |
They seek a highly motivated and creative Research Associate to join the R&D team. You will work within a highly dynamic group and be responsible for developing new applications for RNAscope technology and support our assay services business. Responsibilities: Execute Custom Assay Services (CAD)/PAS projects, including but not limited to ISH-IHC, pre-project proof of concept/probe validation, troubleshooting and others. Focus will be ISH-IHC and new application development to support ISH business expansion and accumulate more in-house experience for new technology development. Responsible for experimental design, assay running, data collection and interpretation. | 11/18/2020 |
| 191 | Trevigen Minneapolis, MN Advanced Research Associate Masters Degree Exp: Up to 2 Years |
The major responsibilities of this position are to primarily develop plate-based ELISA products related to Bio-Techne's existing product lines, including literature review, data analysis, reagent evaluation, feasibility, assay optimization, stability studies and product transfer. Additional work on protein chemistry, antibody evaluation and collaboration with other internal development teams may be needed. Other responsibilities: Develop new immunoassay products. Under general supervision, independently schedule, plan, perform and report experiments for the feasibility, optimization, transfer and validation of immunoassay kits. Evaluate critical raw materials. Optimize formulations and procedures to meet all assay specifications. Understand biological attributes of assay targets by reading literature and defining design goals. | 11/18/2020 |
| 192 | Trevigen Devens, MA Advanced Quality Technician Science or Quality Related BS Exp: 1+ Years |
Advanced Quality Technician reports to the Quality Control Manager and is responsible for in-process and final QC testing of Bionostics products. In addition, Advanced Quality Technician participates in instrument validations, performs lab maintenance activities, initiates collaborations, monitors laboratory and process inventories, conducts device history record review, and creates certificates of analysis for commercial products. Responsibilities: Understands and adheres to all quality technician job requirements. Follows work instructions carefully and demonstrates good documentation practices. Documents results, processes testing, and refers to past batch records when needed. Compiles, analyzes and reports on data conformity | 11/18/2020 |
| 193 | Trevigen Minneapolis, MN Advanced Research Associate - Molecular Biology MS in Molecular Bio, Cell Bio, or Equivalent Exp: 0-2 Years |
The responsibilities of this position are to assist the protein product development team in recombinant protein expression. This includes the preparation of eukaryotic expression vectors, cell culture, and screening procedures. The position involves various techniques such recombinant DNA cloning, DNA preparation, mammalian and insect cell culture, transfections, Western blotting, ELISA, and flow cytometry. | 11/18/2020 |
| 194 | Ultivue Cambridge, MA Laboratory Technician (Assay Development) Minimum of BS in Chemical, Physical, Biological, Clinical Lab Science or Related Exp: 0-1 Years |
The laboratory technologist will support contract research offerings as part of Ultivue’s Assay Development and Services Laboratory. Laboratory work utilizes Ultivue’s InSituPlex™ technology for fluorescence multiplex IHC (mIHC). The lab technician will support routine testing and QC procedures. Technician may take part in basic assay optimization and multiplex panel development activities to support services and U-VUE kits offerings. Responsibilities: Follow laboratory protocols and safety regulations in accordance to a quality management system (QMS). Edit SOPs in continued effort towards regulatory compliance. Perform routine logging of specimens and documentation of sample testing into Ultivue’s laboratory management information system (LIMS). Perform related laboratory maintenance, such as ordering supplies, managing inventory, managing and maintaining equipment, and documenting laboratory conditions. Perform routine and testing of InSituPlex™ assay utilizing specific standard operating procedures (SOPs). Assist pathologist and Ultivue scientific staff in imaging and test support. | 11/25/2020 |
| 195 | Ultivue Cambridge, MA Document Control Specialist BS in Biology or Related Life Science Exp: 1+ Years |
The Document Control Specialist will support the Quality Management System (QMS) by assuring that all controlled documentation for products are in compliance with current Good Manufacturing Practices (FDA), ISO 13485, EU and Health Canada regulatory requirements, as required and will report into the Senior Director of Quality & Regulatory. Responsibilities: Under the direction of the Head of Quality, the Document Control Specialist is responsible for supporting all documentation and training needs. Lead Ultivue’s training program for all employees by monitoring, scheduling, and documenting training. Train new Quality Assurance staff as needed. Provide documentation and training coordination services including numbering, version control, formatting, processing, and filing of documents. Create training profiles, update training profiles on paper and in electronic system, create training reports, maintain training records, etc. | 11/25/2020 |
| 196 | Getinge Wayne, NJ Complaints Analyst I BS in Related Science or Technology Field Exp: 0+ Years |
Responsibilities: Work in a team environment with members of the SSU and QA-Product Surveillance groups on receiving complaints in the complaint system. Work in a team environment with members of the Engineering and Medical teams on completion of Decision Tree (DT) and completion / submission of Initial MDRs. Work independently and with different parts of the organization/departments to perform Good Faith Effort (GFE) to obtain required / additional event information and request sample return. Ensure complaints are handled in compliance with applicable regulations and regulatory standards. Accountable for compliance with all Food & Drug Administration (FDA) and European Union Medical Device Directives (MDD) regulations governing adverse event reports such as Medical Device Reports (MDR) and Medical Device Vigilance (MDV) and reportability requirements for various countries. | 11/25/2020 |
| 197 | Vaxart San Francisco, CA Quality Control Analyst I BS in Scientific Discipline Exp: 0-1 Years |
QC Analyst I is responsible for performing drug substance and drug product in-process, release, and stability testing activities in support of CGMP manufacturing of clinical trial materials. This candidate will also be responsible for providing support to R&D for analytical development and other activities as assigned by supervisor. Other responsibilities: Provides QC support to development and manufacturing in the form of CGMP assay support involving release and stability testing. Performs product characterization activities, including: potency assays, drug product physical characterization, and stability assessment. Performs work necessary to implement procedures appropriate for analysis of drug substance and drug product clinical trial and development materials. Maintains the QC laboratory. | 11/25/2020 |
| 198 | Vaxcyte Foster City, CA Associate Scientist/Engineer, Polysaccharide Process Development BS/MS in Bioprocess Engineering, Chemical Engineering, Microbiology, or Related Exp: 1+ Years/0+ Years |
Vaxcyte is looking for an energetic and talented associate scientist/engineer to contribute to the Polysaccharide development and manufacturing group within the CMC team. Vaxcyte is developing a multi-valent polysaccharide-based conjugate vaccine, based on a novel carrier protein produced using the Xpress CF platform. Polysaccharides are a critical component in conjugate vaccines. The successful candidate will have some practical laboratory experience developing processes related to fermentation, microbiology, biopharmaceuticals, or vaccine industries. The candidate will be eager to utilize and learn new laboratory skills as this person will be responsible for collaboration on experimental design and execution of experiments to further the polysaccharide development program. This position will require >60% time in the lab and this person will be able to independently detail experimental procedures/results to colleagues. The successful candidate will work within the polysaccharide development team to design and execute experiments, summarize pertinent data and present experimental results internally. | 11/25/2020 |
| 199 | VGXI Woodlands, TX Process Technician BS in Life Sciences Exp: n/a |
Responsible for the implementation of cGMP in the pilot plant. Write and review SOPs and production batch records. Implement production processes for the manufacture of plasmid DNA. Conduct cGMP production of plasmid products on an ongoing basis. Other responsibilities: Manufacture plasmid DNA conforming to GMP guidelines. Assist in scaling-up processes to meet growing demands. Write standard operating procedures. Execute validation protocols. Prepare solutions and materials required for the process. Follow batch records or SOPs to conduct cell banking, fermentation and purification processes for plasmid DNA manufacture at research or GLP scale. Conduct miniprep, concentration and gel analysis to in-process samples of research and cGMP productions. | 11/25/2020 |
| 200 | ViaCyte San Diego, CA Manufacturing Associate I BS/MS in Biological or Engineering Science Exp: 1+ Years |
The incumbent will perform a broad range of tasks in the cGMP manufacture of cells and combination cell therapy/device products for use in clinical and developmental studies. This position includes hands-on participation, including materials logistics, assisting in manufacturing operations, and may include non-routine development activities. This is a full-time position. Requirements: Assist in manufacturing operations to produce GMP grade PEC-01 and Combination Product to meet corporate goals. Assist in ensuring that there are sufficient materials available for all production runs or campaigns, including media, small molecules, and growth factors. Provide hands-on support for scale-up and development activities as needed based on a demand plan. Understand and review applicable GMP documentation, including batch records, SOP’s, deviations, change requests, CAPA’s, IOQ’s, technical reports, and other documents. Maintain current training status for all applicable activities. Assist in maintaining GMP areas in a constant state of inspection readiness related to equipment and area preventive maintenance, calibration, and certification. Throughout the course of all job activities, maintain accurate records and documentation required to support regulatory submissions, and comply with regulatory requirements. | 11/25/2020 |
| 201 | Vivex Biologics Miami, FL Process Engineer I BS in Biomedical 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 equipment qualifications and process validations. 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. Other responsibilities: Generate and execute protocols to perform equipment qualifications and process validations. Use LEAN Manufacturing principles to analyze processes and make recommendations for improvements. Lead efforts to solve problems using formal problem resolution techniques and root cause analysis. Create and communicate project plans with detailed tasks and timelines necessary for project completion. | 11/25/2020 |
| 202 | Vivex Biologics Miami, FL Tissue Processing Technician I College Degree in Related Field Preferred Exp: 1+ Years |
The Tissue Processing Technician I supports the Tissue Processing Supervisor in the cleaning, cutting, shaping, inspecting, and packaging of tissues for transplantation. The Tissue Processing Technician I is also responsible for complying with the quality assurance requirements and quality system goals of the bank as mandated by federal, state, and trade regulations. Other responsibilities: Preparation of clean room and clean room procedures as specifically described in SOPs. Preparation of aseptic processing, environmental set-up including all equipment supplies and monitoring of sterile rooms. Processing of all allografts for clinical such as bone, soft tissues, skin, autografts and other tissues as instructed by Processing Supervisor or designee. Preparation and preservation of all types of bone for cutting and shaping into allografts. | 11/25/2020 |
| 203 | Vivex Biologics Miami, FL Donor Development Coordinator BA/BS in Medical Field Exp: 1-3 Years |
The Donor Development Coordinator acts as a donation specialist facilitating the potion of tissue and eye donation. Works as a liaison between the Donor Referral Center and Medical Examiners Offices, law enforcement agencies, and hospitals to ensure quality tissue is recovered. Responsibilities: Works directly with the Donor Services representatives & Donor Management Coordinators on a scheduled or emergency basis and evaluates potential donors by contacting hospital staff and collecting and reviewing all relevant medical records to properly screen a donor and to determine suitability. Approaches NOK of potential donor to request tissue donation. Completes Authorizations and conducts/documents DRAI Interviews with the NOK/designated historian according to FDA Regulations, AATB Standards, and UMTB Donor Services Foundation protocols and policies. Completes all required case paperwork and documents and insures delivery of said paperwork to appropriate departments and triage donor per protocol and per the wishes of the donor and/or donor's family. | 11/25/2020 |
| 204 | Vivex Biologics Miami, FL Product Service Specialist BS in Related Healthcare Field Exp: 1+ Years |
Responsible for the delivery of superior customer service through the use of effective communication and coordination in the receipt, processing, and placement of allograft tissue orders from customers and/or distributors of the tissue bank. Handling allograft orders demands a great deal of attention, detail orientation, and management of time to ensure that allografts reach the desired destination. Builds and maintains business relationships with clients by providing prompt and accurate service to promote customer loyalty to Vivex Biologics, Inc. Other responsibilities: Serves as the first point of contact for general inquiries such as pricing, product availability, and allograft-related technical questions. Ability to identify customer needs and offer product substitutions based on surgical procedures or historical data. Responsible for initiating calls to existing and potential customers to generate revenue for direct distribution. Coordinates the demands and needs of international distribution commitments of the tissue bank to include, tissue allocation, request for tissue production, shipping/customs documentation, and certificate of conformance (if applicable). | 11/25/2020 |
| 205 | Wave Life Sciences Cambridge, MA Associate Scientist, Medicinal/Organic Chemistry MS in Chemistry or Related Field Exp: 0-3 Years |
WAVE Life Sciences is seeking a highly motivated synthetic organic chemist to join its medicinal chemistry team in Cambridge, Massachusetts. This is an ideal position for an individual who is interested in learning cutting edge technologies and who thrives in a team-oriented, fast-paced, and cross-disciplinary biotech environment. The candidate will be responsible for planning, designing and executing multi-step synthesis including purification and compound characterization. Collaboration with colleagues across disciplines, participation in project team meetings, and contribution toward creative problem solving are all encouraged. Other responsibilities: Under general supervision, perform multi-step organic synthesis, operates scientific equipment and instruments, analyze data and prepares related reports. Familiar with the operations involving large scale synthesis. Maintain detailed records of experimental protocols and data in accordance with company policy. Presentation of results in both written and oral format and delivery of completed reports within a multidisciplinary team. | 11/25/2020 |
| 206 | CROWN Johnson City, TN QA Specialist BS in Scientific or Related Discipline Exp: n/a |
The QA Specialist is responsible for performing Quality compliance activities on the plant floor and ensuring that all activities are in compliance with company and regulatory guidelines and procedures. In addition, the QA Specialist is also responsible for assisting in activities directly related to batch release, and batch record and procedure review, revision and approval. The QA Specialist is required to consult with the Quality Management on all serious issues that may impact the company or product. | 11/25/2020 |
| 207 | CROWN Johnson City, TN QC Analyst/Chemist BS in Chemistry Exp: 0-3 Years |
The QC Analyst is responsible for performing testing of raw materials and components, finished products, and stability samples as well as in process tests. In addition, the Analyst is also responsible for assisting in the maintenance and calibration of analytical instruments, preparation of standard and sample solutions and maintenance of associated records. Other responsibilities: Position requires familiarity with HPLC, GC, UV-Vis, IT, and titration as well as standard wet chemistry including, but not limited to, viscosity, pH, etc. Position will also perform peer review of other chemists work and take part in the training program as requested. Position will also be responsible for helping to create and update procedures and documentation for performance lab related activities. Perform investigations as required in accordance with company and regulatory guidelines. | 11/25/2020 |
| 208 | CROWN Dallas, TX Medical Affairs Specialist BS in Medical Related Field or Life Science, Graduate Degree Preferred Exp: 1+ Years |
The Medical Affairs Specialist collaborates with members of cross-functional teams to prepare high-quality correspondence, study protocols, investigator brochures, synopses, regulatory documents, medical and clinical publications, and related medical and clinical documents within agreed-upon timelines. Responsibilities: Prepares, edits, and finalizes protocols, medical affairs scientific presentations, abstracts, manuscripts, and correspondence. Participates in scientific communication planning, including development of strategic medical communication plans, publications in Medical and Scientific Journals, online webinar content creation. Supports the writing, review, and edit of Marketing and Medical Affairs/Clinical Development materials. Partners with the study biostatistician to engage early with the study team including participation in the review of mock and/or blinded tables, figures, and listings (TFLs), and narrative planning for relevant documents. Works closely with the study team to ensure that results and messages in clinical documents accurately reflect the data in TFLs and other information sources. | 11/25/2020 |
| 209 | UBC Blue Bell, PA Safety Data Associate BS in Science or Health Related Field, Pharmacy or Nursing Exp: n/a |
This position is primarily responsible for supporting all operational functions within the Global Pharmacovigilance department. Other responsibilities: Is responsible for the monitoring on a daily basis of the PV mailboxes, fax machines sharepoints/portals and acknowledging receipt of safety case reports. Is responsible for Book-in, duplicate check and accurate full Data Entry of safety case reports into safety database in a timely manner. Generates draft case narrative as assigned by UBC PV Management. Produces assigned work at high quality and according to timelines. Assists in the timely distribution of safety reports to Health Authorities, clients and client partners, in the appropriate format. | 11/25/2020 |
| 210 | 10X Genomics Plesanton, CA Research Associate 2 - Molecular Biology/Product Development MS in Molecular Bio, Biochemistry, Genetics, Microbiology, Analytical Chemistry or Related Exp: 1+ Years |
This is a unique cross-disciplinary position that will work closely with a variety of groups including Molecular Biology, Chemistry, Microfluidics, QC, and Manufacturing, to develop and validate novel reagents for the rapid expansion of 10x product lines. Candidates must have a broad working knowledge of molecular biology and be able to apply that knowledge creatively and independently in a fast-paced work environment. The successful applicant will have exceptional attention to detail and the ability to meticulously execute and analyze highly complex experiments. Previous industry experience is essential. | 11/25/2020 |
| 211 | 10X Genomics Plesanton, CA Process Engineer - MES MS in Statistics, Process Chemistry, Chemical or Manufacturing Engineering or Related Exp: 1-3 Years |
10x is looking for an outstanding Process Engineer to join the Process Development team. This is a key position for the commercialization of consumable products associated with Next Generation Sequencing chemistries. This person will be responsible for developing and integrating process control and yield optimization solutions for complex reagent manufacturing workflows and identifying process to function relationships. The ideal candidate will have a strong background in statistics and data analysis. Knowledge and hands on experience with trend analysis, yield enhancement methods, correlation and ANOVA analysis, quality systems databases, developing statistical process control for reagent manufacturing and previous experience in manufacturing SPC are required. | 11/25/2020 |
| 212 | 1910 Genetics Cambridge, MA Research Associate - Biology BS/MS in Biology, Cell Biology, Molecular Biology, Biochemistry, Pharmacology, or Equivalent Exp: 0-3 Years |
Responsibilities: Executing high throughput screening (HTS) assays in strict accordance with the NIH NCATS Assay Guidance Manual. Developing and validating HTS biochemical assays for characterizing the activity and selectivity of potential drug candidates. Developing and validating HTS cell-based assays for characterizing the activity, selectivity, and cellular permeability of potential drug candidates. Performing a wide variety of experiments across molecular biology, cell biology, biochemistry, in vitro pharmacology, and in vivo pharmacology. Rigorously documenting all experimental procedures, data, results, manuals, etc. in an electronic laboratory notebook (eLN). Leveraging internal and external personnel to troubleshoot experiments. Effectively communicating research results both verbally and orally. Managing all external CRO relationships and cross-checking externally generated results with internal references and/or expectations. Managing all aspects of lab operations such as ordering, organizing, and restocking reagents, equipment, and other supplies. | 11/25/2020 |
| 213 | Sinclair Research Auxvasse, MO Histology Technician BS with focus on lab processing Exp: n/a |
In this role, you will prepare histologic samples for evaluation in a pre-clinical research setting. It will be your job to not only prepare slides but monitor instrumentation and maintain laboratory supplies and cleanliness according to regulations. Throughout the day, you may check-in histology samples, trim tissues and prepare slides, or perform staining and microtomy. You will also assist in developing and implementing new processes while training research staff proper collection procedures. Strong leadership, organizational and analytical reasoning skills are a necessity. ASCP HT or HTL Certification is strongly preferred. | 11/17/2020 |
| 214 | Sinclair Research Auxvasse, MO Study Coordinator BS in related field Exp: n/a |
The ideal candidate will have experience in animal handling and basic research techniques such as sample collection and data recording. As a Study Coordinator, you will help in all these areas, as well as overseeing the daily data collection and study conduct of our animal technicians and junior veterinary staff. It will be your responsibility to ensure they have a clear understanding of study protocol and activities. You will assist in planning out the study timeline, ordering supplies, developing forms, and managing pre-study meetings under the direction of a Study Director. You will be in a strategic role helping not only oversee studies for senior research staff, but communicating with our clients, other departments, and helping teach our animal technicians proper procedure and study conduct. | 11/17/2020 |
| 215 | Singota Solutions Bloomington , IN Production Operator BS Engineering or Science Exp: n/a |
Production operators actively participate in all the manufacturing operations for the company including sampling/dispensing, drug product formulation, aseptic filling, finished dose labeling/kitting/packaging, and packaging component inspection (PCI). Responsibilities: Installing machine change parts and load recipes on fill machine. Staging/loading of components and preparation of fill path. Performing cleaning and VPHP decontamination of isolators. Assisting with environmental monitoring. Assist in process investigations, writing of deviations, and implementation of CAPAs to continuously improve operations. Comply with quality and safety management systems including requirements for documentation, training, system use, SOPs, processes and procedures. | 11/17/2020 |
| 216 | MicroVention Terumo Aliso Viejo, CA Engineer I/II (EIT) BS in Mechanical, Biomedical, Electrical, or Industrial Engineering, or Chemistry or Related Discipline Exp: 0-2 Years |
The Engineer I/II (EIT) supports development of medical device products with work including writing or verifying specifications, designing new products, fixtures, test processes, equipment and specifying raw materials to ensure the concepts and/or prototypes meet their requirements. Typical job duties might include developing new product concepts and products, engineering design and process development, generating intellectual property and writing invention disclosures, supervising assemblers, technicians, and specialists, and largely self-directed, capable of meeting project goals with moderate supervision. This 24-month rotational program is designed to train new Engineers on various aspects of MicroVention - Terumo technology, procedures, and processes. | 11/17/2020 |
| 217 | Akorn Pharmaceuticals Somerset, NJ Aseptic Core Monitor Scientific degree preferred, microbiology Exp: 1 year |
Under the general supervision of the Supervisor, Aseptic Core Monitoring, the Aseptic Core Monitor oversees all activities in the aseptic environment to ensure continual compliance with cGMP and provides mentoring on aseptic technique for all aseptic personnel. This position requires expertise in all aspects of product manufacturing, 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 aseptic manufacturing environment. Responsibilities: Complete daily visual audits of Aseptic Behavior inside the core during setup, formulation, fills, and sanitization processes. Navigate, Manage, and Mitigate Aseptic Risk. Partner with all cross functional groups to make recommendations for enhancements to aseptic process. Complete regular inspections of the physical conditions of the aseptic core including but not limited to floors, ceilings, doors, and walls. | 11/17/2020 |
| 218 | Sorrento Therapeutics San Diego, CA Manufacturing Associate I (Upstream) BS in Life Sciences, Chemistry, or Chemical Engineering Exp: 1-3 Years |
Sorrento is currently seeking a Manufacturing Associate who will be responsible for performing Upstream manufacturing tasks including tracking and control of raw material inventory; maintenance and operation of equipment in cGMP facilities; preparation of buffer and media; and assistance in operation of single use bioreactors for production of clinical and commercial products. Responsibilities: control and track raw material inventory, maintain and clean cleanroom facility and equipment, perform daily monitoring of equipment and assist Facilities and Engineering personnel as necessary on equipment maintenance and calibration, prepare media and buffer solutions, maintain cell culture flasks using good aseptic technique, assist in the operation of Single-Use Bioreactors, including the Wave Cellbag bioreactors and HyPerforma 100L, 500L, and 2000L systems. | 11/17/2020 |
| 219 | Sorrento Therapeutics San Diego, CA Manufacturing Associate II (Downstream) BS in Life Sciences, Chemistry, or Chemical Engineering Exp: 1-3 Years |
Sorrento is currently seeking a Manufacturing Associate II responsible for performing downstream manufacturing tasks including tracking and control of raw material inventory, maintenance and operation of equipment in cGMP facilities, buffer preparation, assisting in setup and operation of purification equipment for production of clinical and commercial products. Responsibilities: assist in setup and operation of the filtration systems (depth filtration, sterile filtration, viral filtration, and UF/DF) including aseptic technique, review and revise cGMP Batch Production Records, SOP’s, protocols, and reports, provide support to cross-functional teams to meet production or timeline demands, demonstrate understanding in technical operations, safety, and Good Manufacturing Practices, and ensure the completeness and accuracy of manufacturing documentation per approved procedures. | 11/17/2020 |
| 220 | Sorrento Therapeutics San Diego, CA QA Specialist AA/BS in Life Sciences, Chemistry, Biology, or Microbiology Preferred Exp: 1-2 Years |
The QA Specialist’s responsibilities are divided into three primary functional areas: Raw Material Inspection and Release, Label Generation, and Document Control. Raw Material Inspection: Associate is responsible for inspecting in-coming raw materials, releasing raw materials, obtaining and submitting test samples to the appropriate contract laboratory, and coordination of receipt of test results. Label Generation: Associate is responsible for ordering label and ribbon stock, generating Master Label templates from approved label specifications, producing labels for specific product lots, ensuring labels are verified as correct and are released in time to meeting the manufacturing schedule. Document Control: Associate is responsible for document control system, including but not limited to change control, word processing, training and equipment database, and maintenance of documents and document site; in addition, the associate shall assist with investigations as directed by QA Management; assist in the execution of validations, or other duties assigned by the head of QA. | 11/17/2020 |
| 221 | Sorrento Therapeutics San Diego, CA Quality Control Microbiology Associate BS in Microbiology Exp: 1-2 Years |
This individual will contribute to providing microbiological support and testing of cGMP environments, as well as contribute to in-process, drug substance, and drug release testing. Responsibilities: Environmental monitoring of cGMP cleanrooms per FDA and USP guidelines, sampling of utilities (i.e. water, clean compressed air), input and manage environmental data, conduct QC testing of raw materials and utility samples; QC tests include, but not limited to bioburden, endotoxin, total organic carbon, conductivity, osmolality, and pH, initiate and participate in environmental excursions and OOS investigations and assess potential impact on product, maintain the QC Microbiology laboratory including ordering materials, inventory control and general lab housekeeping while sustaining safety standards, assist in qualification of test methods, equipment, and processes. | 11/17/2020 |
| 222 | Sorrento Therapeutics San Diego, CA Research Associate BS/MS in Biology, Biochemistry, Chemical Biology, or Related Exp: Seniors/Recent Graduates will be considered |
Responsibilities: execution of cell-based assays to support characterization and development of lead candidates, aid in mechanistic and target validation studies using ELISA, SDS-PAGE, Western Blot, and flow cytometry, maintaining various cell lines for cell-based assays, assist in mAb/conjugate purification and buffer exchange, partake in instruments’ maintenance and calibration, lab cleanliness and orderliness, as well as ordering and replenishing stocks, analyze data and interpret results, keep clear and accurate records for both laboratory notebook and reports. | 11/17/2020 |
| 223 | Sorrento Therapeutics San Diego, CA Research Associate I/II BS in Life Sciences Exp: 1+ Years |
The Oncolytic Immunotherapy group is seeking a highly motivated Research Associate to support the scientific goals of the research group by providing molecular biology, cell biology and virology support for oncolytic virus research and production. The candidate will also assist in the organizational aspects of the research group, such as spreadsheet and database maintenance. Responsibilities: assist in the cloning and screening of plasmid expression constructs for oncolytic virus development, assist in the molecular characterization of oncolytic virus candidates, including DNA and protein purification, PCR, sequencing analysis, and various protein expression analyses, perform maintenance of mammalian cell lines for virus production and characterization, perform standard virology procedures, including infections, plaque assays, and virus purification. | 11/17/2020 |
| 224 | Sorrento Therapeutics San Diego, CA Upstream Process Development and Manufacturing Associate BS in Life Sciences, Chemistry, or Chemical Engineering Exp: 1-3 Years |
The Upstream Antibody Process Development & Manufacturing team is currently seeking an Upstream Associate who will be responsible for performing Upstream process development and manufacturing tasks including cell culture, cell banking, media preparation, benchtop bioreactor operation, and assistance in single use bioreactors operation for production of clinical and commercial products. Responsibilities: assist in the operation of Single-Use Bioreactors, including the Wave Cellbag bioreactors and HyPerforma 100L, 500L, and 2000L systems, review and revise current Good Manufacturing Practice (cGMP), Batch Production Records, SOPs, protocols, and reports, provide support to cross-functional teams to meet production or timeline demands, demonstrate understanding in technical operations, safety, and cGMP, ensure the completeness and accuracy of manufacturing documentation per approved procedures. | 11/17/2020 |
| 225 | Solarea Bio Cambridge, MA Discovery Lab Research Associate BS/MS in Life Sciences related discipline Exp: 0-2 Years |
Solera Bio is seeking a Research Associate with experience working with bacteria and/or fungi with proficiency in aseptic technique, media and buffer preparation, culture inoculation and culture maintenance. The position will be a supporting role for the Discovery Lab with a large focus on culturing of microbes and the identification and quality control of bacterial and fungal strains. Responsibilities: perform culturing of bacterial and fungal strains as well as analytics such as quantifying cell numbers via cell counter, OD600, CFUs, propagate new cultures from parent stocks and perform quality control measures on new stocks/cultures via light microscopy, purity streaking, PCR, DNA extraction and Sanger Sequencing, assist in the manufacturing of microbial biomass for pre-clinical studies, assist in maintenance of routine lab operations through washing of glassware, autoclaving of media, glassware, and lab consumables, ordering and restocking of laboratory supplies, etc., write detailed electronic lab notebook (ELN) entries, analyze and present data in cross-functional team meetings. | 11/17/2020 |
| 226 | Spark Therapeutics Philadelphia, PA Sample Management Associate BS Exp: 0-2 Years |
The Sample/Reagent Technician will perform a variety of sample management tasks including receiving, labeling, transferring, tracking, location management, distribution, archival activities, shipping and disposal of biological samples and reagents. These activities include samples of both clinical and non-clinical origin. These activities will be managed using Laboratory Information Management System (LIMS). Reporting to the Sample Management Lead, this position is accountable for the timely maintenance of an accurate biological and reagent inventory required to support activities for all Research, Clinical and Process Development groups. These activities include working with lab personnel to review sample paperwork against samples to ensure accuracy; communication of discrepancies to appropriate personnel and assistance with problem solving; strict adherence to all procedural SOPs effecting sample handling, storage and documentation; communication of confirmed sample receipts to appropriate internal and external parties; entry and accuracy of all sample information within the LIMS sample tracking systems; distribution of biological samples, sample information and paperwork to scientific staff. | 11/17/2020 |
| 227 | Spark Therapeutics Philadelphia, PA Process Engineer BS/MS Chemical or Biochemical Engineering or related Exp: 1+ Years |
Responsibilities: Provide direction on the Facility and Process Requirements (Both Upstream and Downstream) for new and existing facilities. Be the key point of contact between engineering design firms and internal Spark Manufacturing and MS&T resources. Evaluate conceptual aspects of technical process designs to ensure sound decisions and investments are made in accordance with business strategy and internal policy/governance and assess new innovative technologies. Develop relationships with Roche Engineering resources and leverage existing facility and process designs, requirements documentation, and equipment vendor relationships and other design documentation from Roche. Ensure plans are created and updated in a timely manner, communicated to relevant stakeholders, assess risks, and manage deliverables. Meet scheduled milestones to ensure project/program objectives are met in a timely manner. Use rapid design principles in accordance to Corporate Standards. | 11/17/2020 |
| 228 | Spark Therapeutics Philadelphia, PA Manufacturing Science and Technology Downstream Process Scientist/Engineer BS in Biochemistry or Engineering Field Exp: 0-2 Years |
The Manufacturing Science and Technology (MST) Downstream Process Scientist/Engineer is an entry-level position within the MST Lab team, which is responsible for carrying out laboratory experiments to support clinical and commercial manufacturing of gene therapy products and late-stage process development activities. To support manufacturing, the incumbent will develop an understanding of Spark manufacturing processes in order to assist in the evaluation of raw materials and equipment, investigation of process deviations and development of process improvements. Late-stage process development activities, such as process characterization, will require the incumbent to build an understanding of new processes in the clinical pipeline delivered from the Process Development organization, with whom the incumbent will interact with regularly. The incumbent’s major responsibility in the activities described above is hands-on execution of bioprocessing laboratory experiments for downstream unit operations, such as tangential flow filtration, preparative chromatography and dead-end filtration. The experimental scope spans experimental design, in-lab execution, documentation of results using Good Documentation Practices and data analysis. | 11/17/2020 |
| 229 | Spark Therapeutics Philadelphia, PA Manufacturing Science and Technology Upstream Process Scientist/Engineer BS in Biochemistry or Engineering Field Exp: 0-2 Years |
The Manufacturing Science and Technology (MST) Upstream Process Scientist/Engineer is an entry-level position within the MST Lab team, which is responsible for carrying out laboratory experiments to support clinical and commercial manufacturing of gene therapy products and late-stage process development activities. To support manufacturing, the incumbent will develop an understanding of Spark manufacturing processes in order to assist in the evaluation of raw materials and equipment, investigation of process deviations and development of process improvements. Late-stage process development activities, such as process characterization, will require the incumbent to build an understanding of new processes in the clinical pipeline delivered from the Process Development organization, with whom the incumbent will interact with regularly. The incumbent’s major responsibility in the activities described above is hands-on execution of laboratory experiments for upstream bioprocessing, such as cell culture in flasks and bioreactors. The experimental scope spans experimental design, in-lab execution, documentation of results using Good Documentation Practices and data analysis. The incumbent will also take part in the tech transfer of production processes into clinical and commercial manufacturing suites through interaction with the Process Development organization and both internal and external manufacturing partners. | 11/17/2020 |
| 230 | Spark Therapeutics Philadelphia, PA Quality Assurance Specialist/GCP BS/MS in Life Sciences related discipline Exp: 1+ Years |
This is an entry level role that will be responsible for supporting administrative and operational GCP and GVP audit and compliance activities under guidance and supervision of the Clinical Quality Assurance GCP Lead (and/or designee). This role is meant to prepare/ train an individual to take on a CQA auditor role. Responsibilities: Work with CQA Management to develop CQA business reports, as applicable, support CQA auditors, as needed (i.e. preparation, conduct, follow-up), support CAPA activities, support the development, maintenance, and/or continuous improvement of Global CQA Quality System (SOPs, work instructions, tools, templates, etc.), support applicable Clinical Development, Pharmacovigilance and non-clinical SOP development, training and administration, support the development and tracking of compliance metrics. | 11/17/2020 |
| 231 | SQZ Biotech Watertown, MA Research Associate, Immunology BS/MS in Relevant Field Exp: 0-2 Years/0-1 Years |
This role supports the execution and analysis of experiments and data through technical execution and by supporting experiment planning and organization. This role meticulously documents experiments and their outcomes which helps support potential regulatory filings. Responsibilities: Meticulously execute bench work, analyze data, troubleshoot, and communicate findings; perform in vitro assays using multi-color flow cytometry, ELISA/ELISPOT, and cellular biology methods as well as in vivo studies using murine disease models; optimization of new assays with minimal oversight and analysis of data; gather and critically analyze and experimental data to shape decisions around the direction of studies; deliver biomolecules to cells using the SQZ device; support quality control and review of Investigational New Drug (IND) filings and packages; manage large data sets and compiling data for analysis; contribute to experimental design and project direction in support of team goals. | 11/17/2020 |
| 232 | SQZ Biotech Watertown, MA Research Associate, Immunology (Tolerance) BS/MS in Relevant Field Exp: 0-2 Years/0-1 Years |
SQZ Biotechnologies is looking for a highly motivated, collaborative, and dynamic Senior Research Associate for our Immune Tolerance team within the Exploratory Department. This role is an opportunity to focus on developing novel antigen-specific tolerance therapies for autoimmune diseases and gene therapies. The scope of this work will encompass planning and execution of in vivo and in vitro experiments for various research projects. This position requires effective collaboration within the Tolerance team and regular presentation of scientific results. Responsibilities: perform in vivo studies using murine disease models; deliver biomolecules to cells using the SQZ device; perform in vitro assays using multi-color flow cytometry, ELISA/ELISPOT, and cellular biology methods; execute bench work, analyze data, troubleshoot, and communicate findings; procure, organize, and maintain inventory of materials needed for experiments; contribute to the collective success of the Tolerance team. | 11/17/2020 |
| 233 | SQZ Biotech Watertown, MA Senior Research Associate, Immunology MS in Relevant Field Exp: 1+ Years |
This position works closely with a scientist to design and execute experiments aimed at pre-clinical validation of new cancer treatments. Responsibilities: perform in vivo studies using murine disease models; bench work, analyze data, troubleshoot, and communicate findings; perform in vitro assays using multi-color flow cytometry, ELISA/ELISPOT, and cellular biology methods; optimization of new assays; manage large data sets and help with data visualization; work split between solo and team work, executing on multiple projects simultaneously; possess excellent organizational skills and “can-do” attitude and ability to shift focus based on multiple priorities and deadlines. | 11/17/2020 |
| 234 | SQZ Biotech Watertown, MA Senior Research Associate, Infectious Diseases MS in Relevant Field Exp: 1+ Years |
The Research Associate supports the execution and analysis of experiments and data through technical execution and by supporting experiment planning and organization for multiple projects. Responsibilities: perform in vitro assays using multi-color flow cytometry, ELISA/ELISPOT, and cellular biology methods; gather and critically analyze and experimental data to shape decisions around the direction of studies; procure, organize, and maintain inventory of materials needed for experiments; design, execute and troubleshoot experiments with minimal supervision; contribute to experimental design and project direction in support of team goals; maintain a lab notebook and contribute to supporting documentation when necessary; work with skilled teams in a fast-paced, collaborative, and technical research environment; work independently and execute on multiple projects simultaneously, considering cross-functional projects. | 11/17/2020 |
| 235 | SQZ Biotech Watertown, MA Associate Engineer, Process Development BS in Chemical Engineering, Bioengineering, or related Exp: 0-6 Months |
The candidate will support process development efforts for our clinical and pipeline cell therapy products. Responsibilities: Perform hands-on laboratory work using SQZ proprietary equipment and data analysis; maintain electronic lab notebook, study plans, and experiment reports; support across different functional teams to ensure successful completion of necessary studies; support troubleshooting and identification of corrective actions during the execution of laboratory experiments; adhere to safe laboratory practices; prepare experimental summary presentations to process development team and management; perform data analysis and statistical trending on in-house lab experiments. | 11/17/2020 |
| 236 | SQZ Biotech Watertown, MA Engineer, Process Development BS/MS in Chemical Engineering, Bioengineering, or related Exp: 1+ Years/0-1+ Years |
SQZ Biotech is seeking a highly-motivated Engineer to join their Process Development team. The successful candidate will support process development efforts for our clinical and pipeline cell therapy products. This role will have high cross-functional visibility across the organization. Responsibilities: perform hands-on laboratory work using SQZ proprietary equipment and data analysis; maintain electronic lab notebook, study plans, and experiment reports; collaborate across different functional teams to ensure successful completion of necessary studies; support troubleshooting and identification of corrective actions during the execution of laboratory experiments; participate as person in plant (PIP) for clinical manufacturing; adhere to safe laboratory practices; prepare experimental summary presentations to process development team and management; perform data analysis and statistical trending on in-house lab experiments. | 11/17/2020 |
| 237 | Sunrise Pharma Rahway, NJ Regulatory Affairs Associate MS Pharmaceutical Manufacturing, Pharmacy, Regulatory Affairs, or related Exp: 6+ Months |
Responsibilities include creating & implementing labels for OTC & ANDA submissions, assisting in ANDA submissions using eCTD submission software, preparing & maintaining annual reports, SOP, deviations & OOS reports, and reviewing product complaints & queries & support in developing regulatory strategies & launch OTC products. | 11/17/2020 |
| 238 | Sunrise Pharma Rahway, NJ Production Supervisor BS in related field Exp: n/a |
Responsibilities include production planning, reviewing batch records, maintaining appropriate records/reports, providing training to production/packaging personnel; overseeing production technicians and providing technical assistance when needed, such as maintenance and programming of production machinery; writing validation protocol and equipment performance qualification protocols and writing standard operating procedures for production and manufacturing areas. | 11/17/2020 |
| 239 | Synthorx La Jolla, CA Research Associate II MS in Biomedical Sciences or related field Exp: n/a |
Responsibilities: Performs protein titer determination of fermentation pellets and in-process samples using HPLC and mass spectrometry. Executes SEC, IEX and RP-purity assays following SOPs for product characterization. Performs protein and peptide detection assays using qualitative and quantitative techniques including UV/Vis, SDS-PAGE, and western blot. Assists in troubleshooting and maintaining modern analytical instrumentation. Executes experiments, conducts analysis and reports results. Maintains Standard Operation Protocols (SOPs) and reference materials. Manage and maintain required reagents, laboratory environment, and equipment needed to carry out assignments. Assists research team in protein and peptide purification and prepares samples for mass spectrometry analysis. Prepares research reports and presentations for team meetings. Works closely with team leaders to complete highest priority work to reach goals and milestones. | 11/17/2020 |
| 240 | Talaris Therapeutics Louisville, KY Cell Processing Associate I, Manufacturing Operations BS in related field Exp: 6+ Months |
A Cell Processing Associate I, to be based in Louisville, KY is a production professional responsible for the day-to-day operations related to clinical cell therapy manufacturing in a GMP and GTP compliant ISO 7 classified cleanroom facility. The primary responsibilities of this role focus on cell processing; strong aseptic techniques; adherence to SOPs and cGMP regulations and accurate competition of documentation associated with clinical manufacturing, ability to work in a cleanroom environment (ISO 8, 7, 5); and ability to use manufacturing and cryopreservation equipment, including routine cleaning and maintenance. Secondary responsibilities include development and programmatic organization activities. | 11/17/2020 |
| 241 | T-Cure Bioscience Sherman Oaks, CA Senior Research Associate MS in Life Sciences, Preferred emphasis in Cellular Molecular Biology Exp: n/a |
The Research Associate will assist Senior Scientist with DNA and RNA preparation, molecular cloning, transfection and transduction of human cell lines and retrovirus/lentivirus production. T-Cure provides a competitive salary and excellent benefits and exposure and experience in the growing field of immune-oncology. Responsibilities: effectively communicate with the leadership team, Senior Scientists and fellow researchers for collaborative projects and laboratory duties; participate in laboratory meetings and Journal Clubs and present data displaying the progression of projects and future directions; work with both limited supervision and as a team member; learn new techniques and assays to drive project progression; maintain a laboratory notebook with working knowledge of Good Laboratory Practices (GLPs). | 11/17/2020 |
| 242 | TherapyX Advanced Protein Therapeutics Louisville, KY Project Manager/Executive Assistant MS in Biological Sciences, Biostatistics, or related Exp: 1+ Years |
The candidate will support senior management in enabling all facets of drug and vaccine development, including data management and analysis, as well as the creation of documentation supporting regulatory submissions, applications and final reports. The candidate will also possess the ability to work within a fast-paced multidisciplinary environment to drive the development, implementation and maintenance of software and hardware tools to support and track multiple projects simultaneously. Responsibilities: Work with research and development scientists, in-house, as well as with representatives of diverse CROs and other service providers in multifaceted support of drug and vaccine development; this will include quality control and analysis of internal and external data sets, generation of reports, regulatory documents, etc., as well as the creation and operation of related software and hardware tools. Work closely with in-house and outsourced expertise to add statistical rigor and quality control to analyses and provide concise summaries of key experiments. Bring strong attention to detail to the team along with skills / aptitudes in developing data processing, analysis and communication tools. | 11/17/2020 |
| 243 | Turning Point Therapeutics San Diego, CA Clinical Trial Associate BS or equivalent in scientific or health care field Exp: 1-3 Years |
Turning Point Therapeutics is seeking a highly motivated individual to join the company as a Clinical Trial Associate (CTA) within the Clinical Operations Team, reporting into the Director of Clinical Operations. The Clinical Trial Associate is responsible for the oversight and management of clinical operations activities or projects. The CTA will interact with Clinical Operations teams and collaborate effectively with CROs, vendors and clinical trial sites. The CTA supports the timely conduct of clinical studies according to protocols, Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and all applicable regulations governing the conduct of clinical trials. Responsibilities: Support all aspects of Turning Point Therapeutics’ clinical trials from initiation, planning, execution, maintenance and close-out. Collaborate/Interact with CROs, vendors and clinical study sites. Support patient enrollment and data collection are completed in accordance with study timelines and objectives. Review and assess study documents required for site activation and investigational product release. Review Site selection/Visit reports: Qualification Visits, Initiation Visit Reports and Interim Monitoring Visit Reports on an ongoing basis. | 11/18/2020 |
| 244 | Translate Bio Lexington , MA Research Associate I/II, Formulation Stability BS/MS in Chemistry, Physical Chemistry, Chemical Engineering or Biochemistry Exp: 0-2 Years |
Translate Bio is seeking a highly motivated and scientifically rigorous individual to join the Delivery and Formulation Development team as a Research Associate. The position will focus on stability evaluation of frozen and lyophilized drug products. Responsibilities: Conduct experiments for advancing understanding of stability of lipid nanoparticles (LNP) drug products and provide storage and shipping conditions aligned with success administration of drug product for preclinical and clinical studies. Perform experiments to establish stability parameters, improving physical and chemical stability and integrity of drug product upon long term storage. Support drafting new and revising existing stability protocols for long term stability of drug product. Contribute in writing/reviewing analytical method protocols/stability protocols. Prepare technical reports and presentations for clear communication of scientific findings across interdisciplinary teams. | 11/18/2020 |
| 245 | Translate Bio Lexington , MA Research Associate I/II, Delivery Formulations BS/MS in Chemistry, Physical Chemistry, Chemical Engineering or Biochemistry Exp: 0-4 Years |
Translate Bio is seeking a highly motivated and scientifically rigorous individual to join the Delivery Formulations team as Research Associate I/II. The position will focus on developing novel lipid nanoparticle (LNP) formulations for mRNA delivery for the development of vaccines. Responsibilities: Prepare formulations and perform characterization assays /data analysis with focus on in vivo studies, drug carrier design/development, assay development etc. Support formulation development activities related to increasing stability and formulation optimization. Contribute in writing/reviewing analytical method protocols & stability protocols. Prepare technical reports and presentations for clear communication of scientific findings across interdisciplinary teams. | 11/18/2020 |
| 246 | Translate Bio Lexington , MA Associate Scientist/Senior Research Associate, Plasmid Engineering MS in Chemistry, Physical Chemistry, Chemical Engineering or Biochemistry Exp: 1-3 Years |
Translate Bio is seeking a highly motivated and scientifically rigorous candidate to lead from the bench as an Associate Scientist/Senior Research Associate in the RNA Sciences Team. The position will focus on plasmid synthesis, DNA characterization and supporting the Translate Bio programs and collaborations. The position will be highly collaborative and give the successful candidate a broad range of experience across functions within the organization. Responsibilities: Synthesis, purification, and characterization of plasmid DNA. Support high throughput plasmid synthesis and purification efforts. Support platform projects by performing assays including capillary & gel electrophoresis. Independently design and execute decision-quality research. Prepare technical reports, presentations, and recommendations to management and other stakeholders. | 11/18/2020 |
| 247 | Translate Bio Lexington , MA Associate Engineer, Process Development BS/MS in Chemical Engineering/Biochemistry or a related field Exp: 1-2 Years |
Translate Bio is looking for a highly motivated and scientifically rigorous individual to join the Process Development team as an Associate Engineer. The position will focus on optimization and scale-up of Lipid Nanoparticle (LNP) formulations in support of all vaccine related programs at Translate Bio. Responsibilities: Assist with optimization and scale-up of Bulk Drug Product (BDP) formulation and Final Drug Product (FDP) processes encompassing a wide range of different drug substances and multi-component LNPs. Assist with design and implementation of stability studies focused on identification of formulation conditions resulting in long term stability at multiple storage temperatures. Perform routine and complex analytical methods for characterization of LNP drug products with minimal supervision. Keep detailed records and present study results to R&D and CMC teams as needed. Critical thinking and analysis of data will be central to all aspects of this position. Assist with preparation of technical reports and presentations to clearly communicate scientific findings as needed. | 11/18/2020 |
| 248 | Translate Bio Lexington , MA Associate Engineer, GMP Process Development BS/MS in Chemical Engineering or related field, MS preferred Exp: 1-2 Years |
The Associate Engineer reports to the Senior Engineer and is an integral part of CPD&P team. This position offers opportunities to focus on drug substance and drug product process development, manufacturing, regulatory and analytical support, validation, and data review for drug substances and drug products. The Associate Engineer is responsible for assisting in the development and execution of scalable and robust processes for drug substance and drug product. This position will assist the CPD&P Subject Matter Expert (SME) for process knowledge transfer for drug substance and drug product to support cGMP manufacturing. | 11/18/2020 |
| 249 | Translate Bio Lexington , MA Associate Scientist, Analytical CMC MS in Analytical Chemistry or Biochemistry Exp: 0-2 Years |
The Associate Scientist, Analytical CMC contributes to the analytical development function within CMC and overall CMC strategy of drug development at Translate Bio. The scientist supports the development, validation and transfer of analytical methodologies for incoming raw materials, starting materials, drug substance, and stability testing. The scientist has expertise in biologics, biochemistry, synthetic intermediates, and analytical chemistry. Responsibilities: Help manage analytical chemistry activities both internally and at external contract laboratories for critical raw materials and starting materials. Guide CRO to design and perform phase-appropriate method development, testing, and validation. Manage product stability study programs, trending data. Demonstrate extensive knowledge in state-of-the-art analytical technologies. Authorize/review analytical method development reports, validation protocols/reports, instructions/SOP’s for relevant analytical functions. | 11/18/2020 |
| 250 | Trevigen Wallingford , CT Quality Technician BS in Scientific 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. Responsibilities: Adherence to safety procedures and compliance with department specific SOP’s. Understanding of quality body of knowledge, standard laboratory procedures, and record keeping guidelines. | 11/18/2020 |
| 251 | Trevigen Minneapolis, MN Integration Process Engineer BS Science Related Degree Exp: 0+ Years |
This position is a >75% computer-based position that will focus on the integration of our existing and new product lines into our manufacturing systems (primarily AX). This position will involve taking existing manufacturing documents and processes and enabling them to be integrated and managed in AX, ICA, etc. Projects will be diverse, with primary focus being on established existing product lines, but will also include product lines currently managed outside of AX, ICA or involve the integration of newly acquired product lines from the growing family of Bio-techne brands. Integration of these processes will enable better planning, resource management, reproducibility, reduce back-order times, improve documentation and will facilitate inter-departmental transfers and new product release. This position will also be responsible for assisting the rest of the Process Engineering team as an AX expert and resource during investigation of post-launch manufacturing, QC, marketing, and customer issues. This position will also enable optimization of processes to enhance or improve robust manufacturing of products manufactured at the Minneapolis site. | 11/18/2020 |
| 252 | Trevigen Woburn, , MA Research Associate BS in Biology, Biochemistry, Molecular Biology, Immunology, or related Exp: 0-2 Years |
This hands-on position will support development and troubleshooting of novel polymeric reagents for cell activation, cell separation and other CGT applications. As part of the R&D team, this role will support product development by formulating reagents and testing them in a variety of analytical and cell-based assays. The role will work closely with product teams to develop new products and troubleshoot production of existing products for research and clinical applications. Responsibilities: Characterize hydrogel microparticles via ELISA, microscopy and flow cytometry based assays using established protocols in support of product development and manufacturing efforts. Generate test batches of proprietary hydrogel microparticles using laboratory equipment and functionalize product prototypes with proteins using bioconjugation protocols. Conduct cell-based experiments to evaluate functionality of product prototypes on immune cells. With supervision design, execute and interpret experiments to meet R&D objectives. Collaborate with a diverse team of biologist, chemists and engineers to develop new products for cell and gene therapy applications. | 11/18/2020 |
| 253 | PAR Pharmaceutical Rochester, MI Process Engineer I MS in chemical or other engineering Exp: 1+ year(s) |
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. Process Engineering duties within a single location. Make decisions within guidelines and policies. Follow established procedures to perform assignments, with general instructions on the process and desired outcome. Work is reviewed for soundness of technical judgment and accuracy. etc. | 11/9/2020 |
| 254 | PAR Pharmaceutical Chestnut Ridge, NY Manufacturing Operator l HS diploma or equivalent Exp: 0-2 years |
The Manufacturing Operator I performs functions relating to the processing of drug products, ensuring product compliance to established current Good Manufacturing Practices (cGMPs), customer requirements and in conjunction with all Standard Operating Procedures (SOPs). Follows standard procedures to complete tasks, some of which may vary in scope, sequence, complexity and timing. Learns to apply skills and knowledge to recognize issues and to increase efficiency, throughput and quality. Learns, understands and runs processes to meet the assigned standards/routers and fulfills the assigned schedule; when these are not achieved, may participate in the debrief to understand the reasons why and what needs to be corrected moving forward. Assists in troubleshooting process issues. Responsible for the safe and efficient execution of job duties. etc. | 11/9/2020 |
| 255 | Paragon Genomics Hayward, CA Quality Assurance Specialist BS in molecular biology, chemistry, or other life science Exp: 1+ year(s) |
Paragon Genomics is a fast-growing life sciences company developing advanced reagents and assay kits for next-generation sequencing (NGS). We are seeking a Quality Assurance (QA) Specialist that can help us transition our Quality Management System (QMS) from ISO 9001 to ISO 13485 certification. The QA Specialist ensures compliance with policies and procedures, serves as the main point of contact for customer quality audits and provides quality system performance reports to management. This position will be expected to take a hands-on approach to activities in production and other processes, in order to identify and recommend opportunities for improvement. The QA Specialist will report to the CEO. etc. | 11/9/2020 |
| 256 | Paragon Genomics Hayward, CA Research Associate-R&D BS in biology, molecular biology, chemistry, or related Exp: 0-1+ year(s) |
We are seeking a Research Associate in Molecular Biology to play an important role in the development of novel NGS target enrichment assay technologies and support current operations. This is a laboratory-based position with great career potential for a junior scientist or prospective scientist who already has or wishes to gain hands-on molecular biology experience in the next-generation sequencing space. The candidate should have good interpersonal and problem-solving skills. He/she should be driven to learn and motivated to develop great products. The ideal candidate thrives in a fast-paced and multi-disciplinary environment. This position will report to the Molecular Biology Scientist. etc. | 11/9/2020 |
| 257 | ThermoFisher Scientific Princeton, NJ Scientist II, Process Development MS in biology, chemistry, chemical engineering, or related Exp: Not necessary for MS candidates |
Acts as a key scientist in the upstream process development group within the BioProcess Sciences division of the Pharma Services Group. This position will be responsible for the execution of and hands on support of projects such as the development and characterization of mammalian cell lines for the clinical/ commercial manufacture of recombinant protein products. Participates in the execution of projects developing mammalian cell culture processes to support the production and manufacturing of recombinant proteins (including mAbs) with activities including: Clone and media/feed screening using AMBR technology. Bioreactor culture development including fed-batch (2 to 250L scale) with both glass and single use cell culture technologies. etc. | 11/9/2020 |
| 258 | ThermoFisher Scientific Cincinnati, OH Operator II, Manufacturing HS diploma or equivalent Exp: 1-2 year(s) |
Operators in this position utilize equipment, procedures, and Line Packaging Records (LPR’s) to package batches of product on one or more packaging lines. The Packaging Operator can operate equipment, recognize and remedy quality problems, and perform changeovers and cleanups as required. Perform packaging line operation, including operating/monitoring equipment, inspection, hand cartoning or packing, labeling, palletizing, cleanup, hopper filling, and other duties as required. Assist in Line Clearances between batches, follow cleanup sheet directions, follow verbal orders or requests from group leader/supervisor, and perform other duties as required. Good manual dexterity and fine motor skills needed to carry out the physical aspects of the job. Job requires lifting of materials weighing up to 35 pounds for periods of time. etc. | 11/9/2020 |
| 259 | ThermoFisher Scientific Alachua, FL Associate I, MFG Upstream AS/BS in a related science or engineering field Exp: 1-3 year(s) |
This position entails routine hands-on bioprocess manufacturing within a cGMP cleanroom commensurate with the individual’s level of technical expertise, training, and qualification strictly following defined procedures. What will you do? Perform upstream bioprocess manufacturing in a GMP cleanroom involving adherent and suspension cell culturing while following detailed protocols, PBRs and SOPs. Conduct routine suite cleans, preparation and/or request necessary components and raw materials, labels, etc. to successfully execute production batch records. Adhere to all cGMP procedures and safety/quality standards. Maintain a culture of safety and compliance to all environmental health and safety protocols. etc. | 11/9/2020 |
| 260 | ThermoFisher Scientific San Diego, CA Clinical Research Associate II, In vitro diagnostics BS in a scientific discipline Exp: 0-1 year(s) |
The primary role of this position is targeted toward clinical studies support and study site management. In this role the primary responsibilities include: Coordinating and conducting activities involved in initiating, monitoring, and completing clinical research studies for in vitro diagnostics. Ensuring studies are conducted and documented in accordance with the study protocol, standard operating procedures, good clinical practices and other applicable regulatory requirements. Collect all clinical study essential documents. Participate in lab assessment visits. Ensure that CRO activities and timelines are in coordination with project requirements. Coordinate internal and external clinical studies preparation and planning. Implement and document communication with CRO and laboratories to ensure project progress. etc. | 11/9/2020 |
| 261 | ThermoFisher Scientific Pleasanton, CA Material Handler HS diploma or equivalent Exp: 1 year |
Essential Functions: Receive materials and/or finished goods on a daily basis. Verify the quality, type and amount of materials received are correct and that the appropriate documentation is present (e.g. packing list). Examine, sort, arrange, count, store, pick, and pack items for storage and/or shipment in accordance with established procedures and customer requirements. Prepare routine documentation. Operate material handling equipment (e.g. hand truck, pallet jack, dock lever, etc.). Follow warehouse safety standards and use of proper PPE (Personal Protective Equipment). Prepare and ship materials and/or finished goods in a timely manner according to customer requirements. etc. | 11/9/2020 |
| 262 | ThermoFisher Scientific St. Louis, MO Biopharmaceutical Technician I - Days AS/BS in biology, biochemistry, or chemistry Exp: 0-3 years |
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. etc. | 11/9/2020 |
| 263 | ThermoFisher Scientific Logan, UT BioCenter Assembly Specialist 1 - Second Shift HS diploma or equivalent Exp: 1-2 year(s) |
Responsible for the manufacturing, assembly, and/or packaging of BioProcess Containers in a clean room environment. Technicians carry out the production process by closely following the SOP (Standard Operating Procedures), WID (Work Instruction Documents) and blueprints or drawings as they relate to assembly, materials handling, equipment operation, and finished goods packaging. This position requires following cGMP (Current Good Manufacturing Practices) and working in a fast paced team environment. Key Responsibilities: (Include but are not limited to the following) Follow all safety requirements and cGMP (Current Good Manufacturing Practices) requirements. Follow work instruction document, standard operating procedures and standard works. Assembling product using specific written instructions, blueprints and drawings. etc. | 11/9/2020 |
| 264 | PBL Assay Science Piscataway, NJ Assay Services Scientist I/II/III BS in the life sciences Exp: 1+ year(s) |
The Assay Services Scientist I / II / III works primarily with cell culture-based bioassays, executing antiviral bioassays, ELISAs and other highly sensitive immunoassays for characterizing proteins and reagents; analyzing data and drafting client reports; and developing new and custom assays to support the growth of the Assay Services Group. ESSENTIAL DUTIES AND RESPONSIBILITIES: Execute immunoassays on ELISA, and other highly sensitive platforms like Electrochemiluminescence (MSD), Single Molecule Array (Simoa), and Single Molecule Counting (Erenna). Execute antiviral and antiproliferative cell-based bioassays. Analyze data and write client reports. etc. | 11/9/2020 |
| 265 | PBL Assay Science Piscataway, NJ Quality Control Scientist I BS in the biological sciences Exp: 1-2 year(s) |
To ensure the quality of PBL reagents the Quality Control (QC) Scientist I will perform release and stability testing of interferons, antibodies, and manufactured ELISA kits. In addition, the QC Scientist I will perform bioassays or immunoassays to troubleshoot relevant customer issues and design and initiate experiments and projects to improve the quality of PBL products. The QC Scientist I may also serve as back up to the Product Development, Assay Services, or Manufacturing departments as needed: such additional duties may include designing and performing ELISA testing protocols, custom bioassays, and solution preparation. This individual will be involved with document control, SOP writing, and recordkeeping. etc. | 11/9/2020 |
| 266 | PBL Assay Science Piscataway, NJ R&D Scientist I MS Exp: 0-2+ years |
The R&D Scientist is responsible for the hands-on development of immunoassays, such as ELISAs and cell-based assays, for commercial production. This individual plans and executes design, development, and Manufacturing transfer of bioanalytical assays for product commercialization. The R&D Scientist is also responsible for development of custom assays and reagents for clients. ESSENTIAL DUTIES AND RESPONSIBILITIES: Develops immunoassays and cell-based assays for commercial markets. Executes assay performance verification in multiple biological matrices from normal and diseased organisms. Ensures robustness and ruggedness of assay performance to facilitate ease of large-scale manufacture. etc. | 11/9/2020 |
| 267 | PBL Assay Science Piscataway, NJ Senior Protein Scientist BS/MS in the biological sciences Exp: 1-4+ year(s) |
The Senior Scientist develops and executes purification schemes for new product candidates, develops analytical methods for protein characterization, and enhances current purification procedures with the goal of increasing yield, purity and activity. The Senior Scientist is also responsible for development of custom reagents and assays for clients. ESSENTIAL DUTIES AND RESPONSIBILITIES: Expression, purification, and characterization of recombinant proteins from mammalian and bacterial cell sources. Develops new reagents, such as antibodies or purified proteins, for immunoassay use. Develops and implements new assay methods and technologies for protein characterization. Facilitates the transfer and troubleshooting of new products to the Manufacturing department. etc. | 11/9/2020 |
| 268 | Perrigo Georgia, VT Chemistry Analyst (Tues-Sat 4 PM-12:30 AM) BS in chemistry or related Exp: 1-2 year(s) |
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). etc. | 11/9/2020 |
| 269 | Perrigo Grand Rapids, MI Laboratory Technician (Part-Time) - Oral Care Business Unit [Ranir] BS in chemistry, biology, engineering, or related Exp: 1+ year(s) |
Perrigo Company is dedicated to making lives better by bringing high quality and affordable self-care products that consumers trust everywhere they are sold. Help us do it. RESPONSIBILITIES: Coordinate with internal team to conduct general laboratory work, including liquid formulation batching, wet chemistry and instrumental analysis using specialized lab equipment. Maintain accurate and complete records of testing results and report results to manufacturing and engineering teams. Prioritize workload and departmental needs to a test schedule to meet individual and company deadlines. Maintain all laboratory equipment according to GMP, GLP, and 5S standard; ensure lab meets organization needs for accurate and sustainable test practices. etc. | 11/9/2020 |
| 270 | Perrigo Covington, OH QC Chemist - 1st Shift, 2/2/3 Schedule BS in chemistry, food science, or biology Exp: 1-2 year(s) |
We are currently looking for a highly motivated QC Chemist who will work 1st shift on a rotating 2/2/3 schedule. Description: Collect samples including raw material, finished product, process equipment and environmental. Test purchased materials and/or Perrigo manufactured products per cGMP requirements and participate in laboratory investigations. Operate laboratory equipment. Participate in internal and external quality audits. Maintain personal laboratory work area and assist with general laboratory cleaning. etc. | 11/9/2020 |
| 271 | FCX Performance Carleton, MI Valve Technician HS diploma/AS/AA Exp: 1-3 year(s) |
Essential Functions & Responsibilities: Repair relief valves, control valves, on/off valves and pneumatic actuators in FCX actuation facility or customer plant locations. Mechanically and electrically troubleshoot, inspect, and test valves at specified job worksites. Primary worksites include FCX valve repair centers with occasional customer in-field work sites. Perform pre-testing, disassembly, cleaning, in process inspection, machining, lapping, painting, assembly, testing, and final inspection on various types of valves and actuation. Perform testing on certified test equipment, and complete all documentation by working under a QA / QC / National Board VR program. Complete field service worksheets and submit to job coordinator upon completion of work. Understanding of pneumatic and digital controls. Ability and knowledge to reference appropriate valve manuals for repair requirements. etc. | 11/10/2020 |
| 272 | FCX Performance Lexington, MA Pipette Calibration Technician - FCX/PCI BS in a life science, engineering, electronics, or related Exp: Not necessary for BS candidates |
Pipette Technicians are expected to take a proactive role in supporting the Pipette Services Team and in providing client pipette support. The Pipette Technician is expected to build a high level of trust with internal and client personnel. This trust is developed through consistently upholding PCI Values and demonstrating Honesty, Integrity, Pride, Accountability, Teamwork, and Commitment. Responsibilities/ Assignments: Pipette Calibration Technician I. Works with basic laboratory instrumentation, as well as operates computer-based applications utilized in a laboratory environment. Further develops technical skill whenever possible through internal or external training programs. Completes calibrations, qualifications, PMs and changes with GxP documentation in an accurate and timely manner and in accordance with PCI and Client Standard Operating Procedures (SOPs). etc. | 11/10/2020 |
| 273 | FCX Performance San Francisco, CA Calibration Technician I - FCX/PCI BS in a life science, engineering, electronics, or related Exp: Not necessary for BS candidates |
Completes calibrations and qualifications in a safe, timely, and accurate manner, following PCI and client specific policies and proposals. Responsible for proper handling and maintenance of PCI and client equipment, including testing and standards equipment. Identifies project supply and equipment needs and conveys to the appropriate resource to ensure availability. Works to understand client needs and requirements through effective communication and develops client relationships through excellent customer service. Ensures client requests are conveyed to the appropriate PCI management resource and met in accordance with management direction. etc. | 11/10/2020 |
| 274 | FCX Performance Appleton, WI Valve Technician HS diploma or equivalent Exp: 1-3 year(s) |
FCX Performance is an Applied Industrial Technologies Company and a leading process flow control company. As a Valve Technician you will be responsible for assembling control valves, on/off valves and pneumatic actuators in our FCX actuation facility. Essential Functions & Responsibilities: Mechanically and electrically troubleshoot, inspect, and test valve assemblies. Understanding of pneumatic and digital controls. Ability and knowledge to reference appropriate valve manuals. Exhibit an ability to effectively communicate with plant personnel regarding valve and instrumentation equipment and customer requirements. Obtain all site specific and safety related training. Assist others as required. Job duties are subject to change as directed by management. etc. | 11/10/2020 |
| 275 | FCX Performance Boulder, CO Calibration Technician I - FCX/PCI BS in a life science, engineering, electronics, or related Exp: Not necessary for BS candidates |
Completes calibrations and qualifications in a safe, timely, and accurate manner, following PCI and client specific policies and proposals. Responsible for proper handling and maintenance of PCI and client equipment, including testing and standards equipment. Identifies project supply and equipment needs and conveys to the appropriate resource to ensure availability. Works to understand client needs and requirements through effective communication and develops client relationships through excellent customer service. Ensures client requests are conveyed to the appropriate PCI management resource and met in accordance with management direction. etc. | 11/10/2020 |
| 276 | FCX Performance Waltham, MA Calibration Technician I - FCX/PCI BS in a life science, engineering, electronics, or related Exp: Not necessary for BS candidates |
Completes calibrations and qualifications in a safe, timely, and accurate manner, following PCI and client specific policies and proposals. Responsible for proper handling and maintenance of PCI and client equipment, including testing and standards equipment. Identifies project supply and equipment needs and conveys to the appropriate resource to ensure availability. Works to understand client needs and requirements through effective communication and develops client relationships through excellent customer service. Ensures client requests are conveyed to the appropriate PCI management resource and met in accordance with management direction. etc. | 11/10/2020 |
| 277 | FCX Performance Raleigh, NC Pipette Technician - FCX/PCI BS in a life science, engineering, electronics, or related Exp: Not necessary for BS candidates |
Pipette Technicians are expected to take a proactive role in supporting the Pipette Services Team and in providing client pipette support. The Pipette Technician is expected to build a high level of trust with internal and client personnel. This trust is developed through consistently upholding PCI Values and demonstrating Honesty, Integrity, Pride, Accountability, Teamwork, and Commitment. Responsibilities/ Assignments: Works with basic laboratory instrumentation, as well as operates computer-based applications utilized in a laboratory environment. Further develops technical skill whenever possible through internal or external training programs. Completes calibrations, qualifications, PMs and changes with GxP documentation in an accurate and timely manner and in accordance with PCI and Client Standard Operating Procedures (SOPs). Always considers safety when executing tasks and projects. Ensures that PCI work areas are safe, neatly organized and professional on-site and in office. etc. | 11/10/2020 |
| 278 | Pharmaron Germantown, MD Associate Bioanalytical Scientist, Accelerator Mass Spectrometry BS/MS Exp: 0-1+ year(s) |
This position is responsible for carrying out sample analysis and data processing within stated timeframes and in accordance with Standard Operating Procedures (SOPs) and Company policies. Contributes to the laboratory and equipment maintenance to ensure efficient operations. Essential Functions: Participate in day-to-day operation of the Laboratory, the analysis of samples and associated duties. Responsible for handling and processing of biological samples including competent handling and pipetting technique. Prepare/review data tables and reports within Laboratory Information Management System (LIMS). Ensure adequate levels of reference materials, control matrix, and project-specific consumables and resources are available to meet the objectives of the study. Prepare/review forms and SOPs. Assist in training personnel in the operation and maintenance of laboratory equipment. Assist in data processing, QC checking and data compilation. etc. | 11/10/2020 |
| 279 | Pharmaron Germantown, MD Laboratory Technician, Accelerator Mass Spectrometry (Germantown, MD) BS/BA Exp: 6-12 months |
We are looking for a Laboratory Technician to work on a full-time basis in our Germantown, MD facility. This position is responsible for carrying out sample analysis and data processing within stated timeframes and in accordance with Standard Operating Procedures (SOPs) and Company Policies. Contributes to the laboratory and equipment maintenance to ensure efficient operations. Essential Functions: To work to the Company’s quality procedures in accordance with GLP and GCP regulations and be involved in working to and generating a culture of continuous improvement. To comply with the Company’s Health and Safety, MOSH and ionizing radiation procedures. To participate in the day‐to‐day operation of the Laboratory, the analysis of samples and associated duties. To prepare, with other staff, Standard Operating Procedures (SOPs) and other generic documents (eg worksheets and spreadsheets) as required. To purchase chemicals and other laboratory supplies, gaining financial approval as appropriate. etc. | 11/10/2020 |
| 280 | Phibro Animal Health Corporation Sarasota, FL Fermentation Technician - Tech II HS diploma or equivalent Exp: 1-3 year(s) |
Osprey Biotechnics is a worldwide leader in the development of bioproducts for a large range of bioremediation and bioaugmentation applications including wastewater, soil/ground water, industrial and consumer products, poultry, and agriculture. We are seeking enthusiastic, team-oriented individuals to join our fermentation group in this full-time position. This position is 1st shift, Monday through Friday from 5:00am - 1:30pm, with some weekend work and OT potential. Key Responsibilities: Understand and perform sterilizing and aseptic technique. Assembly and disassembly of valves, equipment, and fermentation tanks. Ability to assemble and inoculate a tank. etc. | 11/10/2020 |
| 281 | Phibro Animal Health Corporation Sarasota, FL Spray Dry Technician I HS diploma or equivalent Exp: 1-3 year(s) |
Osprey Biotechnics is a worldwide leader in the development of bioproducts for a large range of bioremediation and bioaugmentation applications including wastewater, soil/ground water, industrial and consumer products, poultry, and agriculture. We are seeking enthusiastic, team-oriented individuals to join our down-stream processing group in this full-time, entry-level position. This position is 2nd shift, Monday through Friday from 12pm - 8:30pm, with some weekend work and OT potential. Key Responsibilities: Retrieving materials to spray dry. Operating spray drier and monitoring its automated operation. Recording temperature readings throughout the operation and verifying the chart recording. etc. | 11/10/2020 |
| 282 | Phibro Animal Health Corporation Sarasota, FL Fermentation Technician - Tech I HS diploma or equivalent Exp: 1-3 year(s) |
Osprey Biotechnics is a worldwide leader in the development of bioproducts for a large range of bioremediation and bioaugmentation applications including wastewater, soil/ground water, industrial and consumer products, poultry, and agriculture. We are seeking enthusiastic, team-oriented individuals to join our fermentation group in this full-time, entry-level position. This position is 1st shift, Monday through Friday from 5:00am - 1:30pm, with some weekend work and OT potential. Operation, care and routine maintenance of production scale fermentation and culture processing equipment. Assembly and disassembly of valves, equipment, and fermentation tanks. Cleaning and sanitization of valves, equipment, and fermentation tanks. etc. | 11/10/2020 |
| 283 | Phibro Animal Health Corporation Sarasota, FL Blending Technician HS diploma or equivalent Exp: 1-3 year(s) |
Osprey Biotechnics is a worldwide leader in the development of bioproducts for a large range of bioremediation and bioaugmentation applications including wastewater, soil/ground water, industrial and consumer products, poultry, and agriculture. We are seeking enthusiastic, team-oriented individuals to join our blending department in this full-time, entry-level position. This position is 1st shift, Monday through Friday from 7:00am - 3:30pm, with occasional weekend work and OT potential. Key Responsibilities: Able to perform repetitive blending and line bottling operations. Stand for long periods of time. Basic arithmetic skills such as adding, subtracting, and measuring volume/weight. etc. | 11/10/2020 |
| 284 | Poseida Therapeutics San Diego, CA Research Associate - Immuno-Oncology MS in immunology, molecular biology, or related Exp: 0+ 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 a senior lab member and/or lab director. Responsibilities: These may include but are not limited to: Support preclinical development of CAR-T cellular therapies. Studies may include work with molecular cloning, tissue culture, cell isolation from blood products, virus production, and cell separation. etc. | 11/10/2020 |
| 285 | Precision BioSciences Durham, NC Research Associate I/II, CMC Analytical BS in the biological sciences Exp: 1+ year(s) |
The Research Associate I or II, CMC-Analytical – Cell Biology, will work in the Cell Therapy Bioassay/Immunoassay/Flow Cytometry group of Precision BioSciences. This individual will provide biologic analytical support for Product Sciences and Cell Therapy Process Development projects. The position will contribute to development efforts for CART-cell projects by providing sample preparation and analysis in a timely manner. This position is lab-based and will share facilities and resources with the Cell Therapy teams. Primary responsibilities will include: Design, development, characterization and documentation of analytical methods for the phenotypic characterization of genome-edited cell therapy products. etc. | 11/11/2020 |
| 286 | Precision Medicine Group Norton, MA Biorepository Technician BS in biology, chemistry, or other life science Exp: 0-2 years |
Our Biorepository Technicians assist in shipment and receipt, the retrieval preservation of biological samples that arrive daily or are stored in the repository. Essential duties include but are not limited to: Unpack specimens and record all pertinent information in Incoming Shipment Batch and Incoming folder. Distribute confirmation of shipment receipt form if required by project. Check information on sample vial against information provided by the study site or data coordinating center. Scan samples into data management system, BSI. Ensure paperwork is accurate and inform Supervisor/Manager of any discrepancies. etc. | 11/11/2020 |
| 287 | Precision Medicine Group Chicago, IL Business Intelligence Analyst I - Pharma Analytics BS/BA Exp: 1-3 year(s) |
Business Intelligence Analysts (BIA I & II) play a meaningful role in achieving our team’s goal of exceeding customers’ expectations with leading edge data management and data-driven insights and applications. A Glimpse of What Your Day-to-day will look like: Design, develop and administer a system for self and others to evaluate appropriateness of data for analytic hypotheses and applications. Develop and direct a process to clean and integrate complex healthcare datasets in order to create the data foundation for further analytics, client applications, and the development of key client insights. Contribute client team meetings for client engagements and strategic projects requiring complex data management support. etc. | 11/11/2020 |
| 288 | Precision Medicine Group Norton, MA Clinical Operations Assistant HS diploma or equivalent Exp: 0-1 year(s) |
The Intern/Clinical Operations Assistant will be assigned tasks to assist in the daily operations of the Clinical Affairs department. This position will aid in ensuring a functional, clean work environment and will be responsible for supporting ongoing projects. Essential functions of the job include but are not limited to: Complete directed tasks as specified by Clinical Project Managers. Complete directed tasks as specified by the Data Management team. Appropriate handling of whole blood. Observe PBMC isolation and cryopreservation. Maintain a clean workspace. etc. | 11/11/2020 |
| 289 | Precision Medicine Group Frederick, MD Kit Production Technician HS diploma or equivalent Exp: 1-2 year(s) |
Prepare and ship the important materials used in sample collection to meet our client’s specifications. Essential duties include but are not limited to: Kit Manufacturing: Prepare Sample Collection Kits per Standard Operating Procedures and Project Operating Procedures. Assemble and label Kit Components; including collection tubes, vials, documentation, and boxes per specific Assembly Instructions. Aliquot reagents using Aseptic Technique. Complete Batch Records and supporting documentation. etc. | 11/11/2020 |
| 290 | Precision Medicine Group Frederick, MD Processing Technician AS/BS in biology, chemistry, or other life science Exp: 1-2 year(s) |
This role is responsible for receiving, accessioning, and processing patient samples. In addition to processing blood and leukopaks for our Accucell line of cryopreserved cells. Essential duties include but are not limited to: Process and cryo-preserve fresh biological samples: Receive and inventory all incoming fresh biological samples into electronic LIMS database. Perform cell isolations and/or separate whole blood and body fluids into various components. Perform cryopreservation of all isolated cells. Prepare all reagents used in lab. etc. | 11/11/2020 |
| 291 | Precision Medicine Group Philadelphia, PA Remote - Statistical Programmer I - Clinical Trial Services BS in statistics, mathematics, computer science, or related Exp: Entry level |
What to expect day to day: Create specifications for derived/analysis datasets. Program analysis datasets, tables, figures, and listings to support the analysis of clinical trials data using SAS. Generate SDTM domains, ADaM datasets, and Define.xml files. Provide programming support to supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requests. Perform quality control for SAS programs and other study documents (e.g., presentations and reports). Document the quality control review process. Review output across programs to ensure consistency. etc. | 11/11/2020 |
| 292 | Precision Medicine Group Redwood City, CA Research Assistant - Fresh Biological Samples BS in biology, chemistry, or other life science Exp: 1-2 year(s) |
In this role: You will process fresh patient specimens and nonclinical samples. You will perform PMBC or cell subset isolations, plasma fractionations, serum separations, cell thawing, cell counting and generating whole blood aliquots. You will receive and process nonclinical samples such as whole blood units and/or leukopaks. etc. | 11/11/2020 |
| 293 | Poseida Therapeutics San Diego, CA Research Associate - Immuno-Oncology BS/MS in Immunology, Oncolocy, or Related Exp: 0-3 Years |
Poseida is seeking an outstanding candidate to join the 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 a senior lab member and/or lab director. Responsibilities: Support preclinical development of CAR-T cellular therapies. Studies may include work with molecular cloning, tissue culture, cell isolation from blood products, virus production, and cell separation. Plan and execute flow cytometry based assays for characterization of cellular products and analysis of tissue samples from animal studies. Plan and execute in vitro cell based immunoassays to functionally characterize CAR-T product. | 11/5/2020 |
| 294 | Poseida Therapeutics San Diego, CA Manufacturing Associate BS in Chemistry or Engineering Exp: 0+ Years |
The Manufacturing Associate is part of the Poseida internal manufacturing team in support of Poseida’s clinical production of cell therapies. This position will support front line non-viral cell therapy GMP production activities, process transfers, and technology improvements towards the successful delivery of released product to meet the needs of Poseida’s clinical trials. Responsibilities: Perform critical GMP aseptic operations in ISO 5 and ISO 7 production environments, following paper-based and/or electronic batch records, standard operating procedures (SOPs), policies, and work instructions to ensure safe and compliant operations. Assist with startup activities of a new cGMP facility by collaborating with PD, MSAT, Facilities, and Quality departments. | 11/5/2020 |
| 295 | Poseida Therapeutics San Diego, CA Lab Technician BS Exp: 6+ Months |
Poseida is seeking an outstanding candidate to join the Research Operations team. The Lab Technician is responsible for providing broad support for research personnel by maintaining lab facilities, carrying out basic lab equipment maintenance, washing and autoclaving glassware, coordinate collection of biohazard/chemical waste, and replenishing lab supplies. Responsibilities: Set up and carry out daily operational maintenance of lab equipment. Coordinate routine equipment maintenance and preventative maintenance with various vendors. Provide immediate support and troubleshoot issues that arise in the labs (freezer leaks, centrifuge malfunction, incubator contamination, etc.). Conduct daily lab inspections to look for equipment issues (alarms, leaking freezers, etc.), help create a safe lab work environment, and communicate safety violations or issues encountered to Research Operations team. | 11/5/2020 |
| 296 | PRA Health Sciences Salt Lake City, UT Quality Control Associate HS Diploma Exp: 1-2 Years |
The Quality Control Associate will support the preparation and conduct of studies by monitoring and reviewing study data, by a review of data entry and/or by QC of completed source documents. Responsibilities: May assist in the identification of data entry errors through data entry reconciliation. QC completed source documents. Fully document all completed QC on appropriate forms. Participates in internal team meetings when requested. Ensures all identified errors are resolved in a timely manner. May identify trends in documentation errors by item or staff member. May assist with developing new work methods for data entry and QC of study documentation. Review and QC source documents with the eCRF or draft database as requested | 11/5/2020 |
| 297 | PRA Health Sciences Blue Bell, PA Clinical Trial Assistant BS Highly Preferred Exp: 0-2 Years |
You will be responsible for setting up, tracking and maintaining Clinical Site related documents. You will help manage and review regulatory documents as well as maintain the Local Study File. Assist with coordinating the distribution, retrieval and review of regulatory documents required for the initiation of the Clinical Study, through maintenance, and close-out. Performs the role of Clinical Trial Assistant (CTA) supporting the Local Trial Manager and Site Manager to ensure optimal management of all documents with logistical and administrative tasks related to trial start-up, execution and closing of clinical trials. Performs regulatory document review and approval, including site specific Informed Consents. Ensures trial related activities are in compliance with GCO SOPs, policies and local regulatory requirements. May contribute to process improvement, training and mentoring of other CTA’s. | 11/5/2020 |
| 298 | PRA Health Sciences Boston, MA Clinical Trial Coordinator - Training BS or Higher Exp: 1-4 Years |
The CTC is a detail oriented profession, who supports the Clinical Quality Management department in areas of process, training and compliance, SUSAR distribution, and ensuring that studies are inspection ready. Responsibilities: Distributes SUSAR reports to investigators. Runs and distributes compliance reports. Assists in vendor oversight. Performs QC of documents and participates in revisions. Routes documentation for appropriate signage. Collects, organizes and prepares regulatory documentation for transfer to Trial Master File and assists with tracking of document under guidance. Helps to develop and maintain tracking tools for event investigation, training, SUSAR distribution and inspection readiness. Coordinates meetings, prepares agendas and takes minutes. Responsible for ongoing maintenance of the GCO component of learning portals. Produces metric reports for event investigations | 11/5/2020 |
| 299 | Precision Biosciences Durham, NC Research Associate I/II CMC Analytical BS/BA Exp: 1+ Years |
The Research Associate I or II, CMC-Analytical – Cell Biology, will work in the Cell Therapy Bioassay/Immunoassay/Flow Cytometry group of Precision BioSciences. This individual will provide biologic analytical support for Product Sciences and Cell Therapy Process Development projects. The position will contribute to development efforts for CART-cell projects by providing sample preparation and analysis in a timely manner. This position is lab-based and will share facilities and resources with the Cell Therapy teams. Primary responsibilities: Design, development, characterization and documentation of analytical methods for the phenotypic characterization of genome-edited cell therapy products using multi-color flow cytometry, immunoassay and bioassay. | 11/5/2020 |
| 300 | MacroGenics Rockville, MD QA Document Control Specialist I HS Diploma or Equivalent Exp: 1+ Years |
The QA Document Control Specialist I/II is responsible for executing key document control-related activities that support various departments at MacroGenics. This position is responsible for scanning and performing quality checks of GMP documents. The individual will also provide coverage in the document archive room and assist with organizing, retrieving, and filing GxP documents. The individual must possess the ability to handle multiple priorities, be able to interface and communicate effectively with individuals from various departments daily and be able to work as part of a team. Responsibilities: Scanning batch records, test data, protocols, reports, and placing them into their respective electronic folders daily. Routing, reviewing, and overall management of GxP documents in MasterControl, including SOPs, forms, specifications, and protocols. Conducting quality control reviews of scanned documents for accuracy and completeness daily. | 11/5/2020 |
| 301 | MacroGenics Rockville, MD Bioprocess Associate II MS Biochem/Chem/Life Sciences Exp: 0+ Years |
The Bioprocess Associate II is responsible for all aspects of cell culture process development and validation as well as technology transfer, including process optimization, scale-up, characterization and validation studies, toxicology material production, process transfer to manufacturing, and production support. This individual will also be responsible for analyzing and summarizing the data in technical reports and presentations and troubleshooting as needed. Responsibilities: Design and execute experiments, including shake flasks, production bioreactors, and harvest operations, to support the development of biologics products. Complete documentation to support testing procedures including data capture, forms, logbooks, and inventory batch records. Analyze experimental data for process understanding and further improvements, draw conclusions and interpret results using statistical tools, including media and process development, process characterization and validation. Contribute to authoring of protocols, operating procedures and technical reports ensuring timely and accurate completion. | 11/5/2020 |
| 302 | RedShiftBio Burlington, MA Mechanical Engineer BS/MS Mechanical Engineering Exp: 0+ Years |
RedShift BioAnalytics is seeking a Mechanical Engineer to support the development of analytical instrumentation for the characterization of biologic drugs. The position is both exciting and challenging, with exposure to automation, microfluidics, thermal management, and opto-mechanics in addition to instrumentation design. | 11/5/2020 |
| 303 | Refuge Biotechnologies Menlo Park, CA Senior Reseaarch Associate BS/MS Immunology/Cell Biology Exp: 1-2 Years |
In this role, you will contribute to the company’s efforts to develop next-generation cell therapies in solid tumor malignancies. Specifically, you will be part of a preclinical development team focused on engineering approaches to enhance CAR T anti-tumor activity. The successful candidate will have a strong immunology background and will be expected to work in a collaborative cross-functional team environment, perform experiments, organize and analyze results, communicate effectively and present findings in team meetings. Responsibilities: Employ viral-based strategies for the genetic modification of T cells with chimeric antigen receptors (CARs). Culture and characterize CAR T cells. Plan and execute in vitro functional assays with human T cells according to project timelines and goals. Assist with design of murine models/experiments to evaluate CAR T cell function in vivo. | 11/5/2020 |
| 304 | REGENEXBIO Rockville, MD Validation Engineer BS/MS Engineering or Related Exp: 1+ Years |
You will be responsible for all aspects of qualifying GxP systems including, but not limited to, GxP analytical equipment, controlled temperature units, GMP manufacturing equipment, and GxP computer systems. In addition, you will maintain up-to-date knowledge of validation requirements, practices, and procedures and coordinate with others participating in validation activities. Responsibilities: Develop, collaborate on, and review validation deliverables for equipment and computer systems used in GxP laboratories and manufacturing. Interact with other departments and vendors to facilitate validation deliverable preparation and execution. Write and execute validation protocols in accordance with SOPs and industry standards. Assist with troubleshooting and investigations of validated systems. Conduct periodic reviews and requalifications of systems to ensure they are maintained in a validated state. | 11/5/2020 |
| 305 | REGENEXBIO Rockville, MD Associate Scientist, Bioanalytical Sciences BS/MS Exp: 1-2 Years |
As the Associate Scientist/Senior Associate Scientist of the Bioanalytical Sciences team, you will be responsible for developing and validating bioanalytical methods to support our gene therapy products pipeline. You will have the opportunity to collaborate with many different groups across the organization, including Research and Early Development, Quality, and Clinical Development and may oversee Contract Research Organizations to ensure that all applicable bioanalytical test methods are appropriate for the stage of non-clinical and/or clinical development. Responsibilities: Develop, qualify and/or validate robust bioanalytical methods (ligand binding and/or cell-based assays) to support the Company pipeline. Troubleshoot and resolve analytical method and instrument issues to successful resolution. Keep detailed, accurate testing records and assure that laboratory equipment is calibrated, standardized, and monitored, as appropriate. Author technical documents (analytical method qualification/validation/transfer documents, technical reports, SOPs, etc.). | 11/5/2020 |
| 306 | REGENEXBIO Rockville, MD In-House CRA / Clinical Trial Associate BA/BS Exp: 1-2 Years |
As the In-house CRA you will support and coordinate the logistical aspects of clinical trial management, site management, data review and cleaning according to FDA regulations, Good Clinical Practice (GCP) and relevant SOPs and acts as a pivotal point of contact for the clinical trial team. Under general supervision, you will assist with the coordination of activities associated with the start-up, conduct, and close-out of clinical trials and other duties as assigned. Responsibilities: Assists in the development and editing of study-related materials (e.g. consent forms, study binders, site study aids). Assists with preparation of training workshops, Investigator/Advisory Board meeting materials. Assists with all phases of clinical trial activities (e.g. start-up, conduct, and close-out). Develops study tracking tools (e.g. site lists, enrollment tracking, vendor spreadsheets) | 11/5/2020 |
| 307 | Sanaria Rockville, MD Quality Control Associate BS Exp: 1-2 Years |
This position is responsible for performing routine release and stability testing of final product following cGMP regulations and Sanaria SOP. This position also requires performance of in vitro assay, Viability assay and other QC tests. Responsibilities: Processing and conducting immuno-assays on preclinical and clinical product. Generating and maintaining documentation as per Sanaria documentation procedure. Writing and executing new SOP and protocols. Using technical proficiency and independent thought to collaborate with others to implement new assays. Adhering to industry and government standards regarding aseptic technique and tissue culture practices. Maintaining lab materials inventory and equipment’s. | 11/5/2020 |
| 308 | SCA Pharma Windsor, CT Lab Analyst - Microbiology BS Exp: 0-2 Years |
The Microbiology Laboratory Analyst is responsible for performing laboratory oversight of GMP compounding activities at SCA Pharmaceuticals. The Laboratory Analyst performs Lab investigations, OOL/OOS, executes CAPA's as they pertain to the Microbiology department and supports validation and technical change control activities. This position requires advanced understanding of site processes in order to write technical documents including engineering studies and standard operating procedures. The individual occupying it is expected to be capable of working with minimal supervision. The Laboratory Analyst is expected to communicate well with fellow employees as well as Compounding Operations and Quality Assurance departments. Responsibilities: Perform daily Bacterial Endotoxin testing on all batches/lots of product as part of release testing, and assist with Endotoxin product validation activities as necessary. Write technical documents for Microbiology Lab including standard operating procedures (SOP's), investigations, corrective and preventative action plans. | 11/5/2020 |
| 309 | Scholar Rock Cambridge, MA Associate Scientist, Antibody Characterization BS/MS Molecular Biology/Biochem/Related Exp: 1-3 Years |
The Antibody Discovery & Engineering group at Scholar Rock is developing best-in-class antibody therapeutics to help patients with unmet medical needs. We are seeking an outstanding individual to support the discovery and characterization of antibodies to enable the lead selection for multiple therapeutic programs. The successful candidate will work with the phage display and hybridoma teams to establish and execute biophysical and bioanalytical assays for comprehensive characterization of antibodies. The person in this role will have the opportunity to learn various aspects of biotherapeutic drug development in a fast-paced matrixed environment. Responsibilities: Characterize the binding properties of antibodies by ELISA, flow cytometry, and kinetics tools. Perform stability and pre-formulation studies on antibodies to assess their “drug-like” qualities. Maintain detailed records of experimental protocols and data in laboratory notebooks in accordance with company policy. | 11/5/2020 |
| 310 | Sebela Pharmaceuticals Holbrook, MA Analytical Services Scientist BS, MS Preferred Exp: 1-4 Years |
This is a Laboratory Bench Position for routine/non-routine testing and development/validation of new product testing. Responsibilities: Develop/Optimize/Validate analytical test methods and write protocols/technical reports/test methods in a cGMP environment to support R&D product pipeline requirements. Evaluation of contract laboratory test method validation reports for completeness and adherence to cGMP/USP standards. Perform non-routine evaluation and testing related to investigations and technology. Perform routine laboratory testing. Review analytical data for completeness, accuracy, and compliance. Provide training regarding test methods, equipment, and compliance. Other laboratory duties as assigned. | 11/13/2020 |
| 311 | Sebela Pharmaceuticals Holbrook, MA QC Chemist BS in Chemistry or Related Discipline Exp: 0-2 Years |
This is a Laboratory Bench Position that performs routine release testing for raw materials, intermediates, and final products within a cGMP environment. Responsibilities: Perform testing of raw materials and products. Perform instrument qualification and maintenance. Perform test method validation/verification. Review analytical data for completeness, accuracy, and compliance. Perform training on procedures, equipment, or quality systems. Other duties as assigned. Individual contributor, but may be assigned as a project lead or trainer commensurate with experience or expertise | 11/13/2020 |
| 312 | Seer Bio Redwood City, CA Formulations Research Associate BS/MS Chemistry or Materials Science Exp: 1 Year |
Seer’s new Formulations Research Associate will be responsible for fundamental laboratory organization activities, including inventory, stocking, and the cleaning of laboratory glassware. Responsibilities: Laboratory organization – stocking, inventory and cleaning of laboratory glassware. Support our characterization efforts and execute standard characterization protocols (DLS, XPS, TEM). Assist with materials synthesis, helping to set up reactions and purify synthesized materials. Implementing standard operating procedures for current materials. Effectively present data internally to other Seer scientists and technologists. Enable the efficient operation of our fast-paced laboratory. Execute standard SOPs reliably. Proficiency in sample prep methods for materials characterization. Work with the broader Formulations team in the development of cutting-edge materials. | 11/13/2020 |
| 313 | Seer Bio Redwood City, CA Process Development Engineer BS/MS Chemical Engineering, Chemistry, Materials Science or Related Exp: 1Year |
Reporting to the Associate Director of Process Development, we are seeking an exceptional Engineer to join our team based in our Redwood City office. Experience synthesizing nanoparticles and scaling such complex processes is highly desired. The role requires skills including particle synthesis, surface modification, and incorporates both organic and inorganic chemistry. Seer’s new Engineer will be empowered to assist in the scale-up and manufacture of critical components of our platform. Responsibilities: Support lab activities for synthesizing and scaling nanoparticles and other biosensor samples. Maintain and operate laboratory equipment including balances, reactors, filtration equipment, and particle sizers. Support the company’s interactions with contract development and manufacturing organizations (CDMOs) to source and characterize nanoparticles. Organize, evaluate, and communicate data in an effective and scientific manner. | 11/13/2020 |
| 314 | Nordson Brooklyn Park, MN Production Operator I HS diploma or equivalent Exp: No experience required |
Position Summary: Position consists of assembling and inspecting medical devices in a clean room environment while under general supervision in accordance with specific work instructions and SOPs. Assembly and inspection sometimes done under a microscope. This position requires the ability to work with small tools and assemble small components using a high degree of dexterity and accuracy. This position requires direct contact with an implantable medical device. Essential Job Duties and Responsibilities: Must be able to work under direct supervision and take work instruction from Supervisor and Leads, work cooperatively and productively within a team environment. Ability to do repetitive tasks, Detail-Oriented and adherence to Nordson’s Safety Policy. Read, Understand and follow Standard Operating Procedures without deviating from the outlined process after training has been completed. Ability to work on Development Department process steps with significant Technician oversight. etc. | 10/31/2020 |
| 315 | Nordson Austintown, OH Material Handler HS diploma or equivalent Exp: 1-3 year(s) |
A material handler is responsible for sequencing all WIP, driven by dispatch scheduling, at each relevant machining center to enable work center efficiency and elevate execution of OTD to 90% or greater. Essential Job Duties and Responsibilities: Offloads incoming bar stock. Moves bar stock from storage area into the manufacturing process as required. Reviews machining center daily dispatch reports for machining centers and sequences bar stock in order at the relevant machining center. Transfers bar stock from machining center to machining center to assist operator efficiency. Removes clutter from the process line areas. Removes and disposes of dunnage properly. Empties machining chip hoppers as necessary. etc. | 10/31/2020 |
| 316 | Nordson Brooklyn Park, MN Product Development Technician Supervisor - Nordson MEDICAL AS/AA/BS/BA Exp: 1-3 year(s) |
The Product Development Technician Supervisor is responsible for planning and directing daily activities, in coordination with the Development team, of personnel focused on Development assembly. The supervisor supports goals and objectives according to GMP’s, SOP’s and established policies, practices, procedures, quality, and cost standards. The role focuses on continuously improving efficiencies and working cross functionally to achieve overall company objectives. Essential Job Duties and Responsibilities: Participate in Development project planning to understand upcoming Development needs, changes in schedules, current challenges, and space/equipment allocation to help establish strategies to meet team goals. Act as a cross functional liaison for Development and Operations personnel resource communication and alignment. Manage personnel problems/concerns effectively and act as the primary point of contact for personnel feedback. etc. | 10/31/2020 |
| 317 | Nordson East Providence, RI Machine Technician - 2nd shift HS diploma or equivalent Exp: 1-3 year(s) |
Machine Technician I is responsible for setting up and operating specialized automated production assembly equipment as well as setting up manual jigs and fixtures for secondary operations. Additionally, responsible for detailed record keeping for equipment and production related activities. Essential Job Duties and Responsibilities: Setup and operate automated production equipment. Setup manual jigs and fixtures for production operators. Provide training and instruction to operators on proper equipment operation. Prepare all materials in advance of setup. Record all materials used for each production order for lot number traceability. Monitor production and make adjustments to ensure quality at all times. Keep detailed records of adjustments made during production. etc. | 10/31/2020 |
| 318 | Nordson Loveland, CO Assembly Technician HS diploma or equivalent Exp: 1 year |
Assemble finished goods according to work instructions while maintaining outlined quality procedures. Essential Job Duties and Responsibilities: Assemble finished goods according to work instructions. Sort defective parts as directed by quality control. Able to work in a clean room environment. De-gate parts as required. etc. | 10/31/2020 |
| 319 | Nordson Salem, NH Pre Form Technician Second Shift Temp to Hire HS diploma or equivalent Exp: 1+ year(s) |
To utilize a wide range of equipment, fixtures, gages and hand tools to support the manufacturing of medical device products. To maintain all logs, forms and resulting paperwork. Essential Job Duties and Responsibilities: Understand the need to deliver quality product and demonstrate a commitment to quality. Contribute to continuous improvement and Lean initiatives. Follow clean room protocols for hygiene and gowning. Maintain regular attendance. Must be able to work flexible hours. Trained to all manual preform procedures. Trained to all machine preform procedures. Able to follow written and oral instructions well. etc. | 10/31/2020 |
| 320 | Nordson Loveland, CO Product Equipment Technician HS diploma or equivalent Exp: 1-3 year(s) |
This position is primarily responsible for the set up, troubleshooting, and up-time of various automated and manual packaging equipment. The Product Equipment Technician (PET) works to develop and enhance the programs and setup on these machines to increase accuracy, efficiency, and throughput. The PET will also set up and program automated de-gating equipment used at the press during plastic injection molding operations, and will be instrumental in the development and refinement of programs and processes used by these robotic devices. The PET works daily in the company’s ERP system (IFS) to verify and enter data while ensuring the timely completion of all assignments. This position will ensure proper line clearance of all equipment prior to the start of any new Shop Order while ensuring all packaging equipment is properly set up to accurately and repeatedly produce the required bag sizes, labeling, and part count while validating that the bag appearance and its contents meet the quality expectations of Value Plastics, Inc. Furthermore, this position will serve as a back-up for other responsibilities such as visual AQL inspection and part cleaning operations. etc. | 10/31/2020 |
| 321 | Alvogen Norwich, NY Process Engineer I BS/MS Exp: 0-3 years |
The Process Engineer I reports to the Director of Process Engineering and Technical Services (PETS). RESPONSIBILITIES: Support the development, transfer, and validation of manufacturing processes. Define transfer plan for internally and externally developed products. Utilize a risk based approach to define experimental/feasibility studies. Identify critical process parameters and their impact on product quality. Create and present technical presentations at project milestones. Perform process optimization. Develop and execute process validations. Provide technical support were needed. Administrative duties: Document preparation (plans, risk assessments, DOE, Batch records, protocols, summary reports, investigations, etc.…). Use statistical methods for data analysis. etc. | 10/31/2020 |
| 322 | Nostrum Laboratories Kansas City, MO Packaging Technician HS diploma or equivalent Exp: 1 year |
The Packaging Technician performs routine packaging operations for the production of pharmaceutical products; operates packaging line equipment according to established SOPs and department procedures. Duties and Responsibilities: Prepares and cleans room, equipment, facility and documents for manufacturing and packaging process. Verifies calculations, process steps and yield. Ensures that processes, tools, products and materials meet established quality standards and requirements. Notifies management when inventory fails below certain levels. Assists in the assembly and disassembly of process equipment as necessary. Examines sample of finished product per batch record instructions for conformance with specifications. Notifies supervisor of manufacturing / packaging deviations and assists with proper resolution/documentation. etc. | 10/31/2020 |
| 323 | Nova Biomedical Billerica, MA Manufacturing Engineer – Mechanical BS In mechanical, industrial, manufacturing, or electrical engineering Exp: 1-3 year(s) |
START YOUR APPLICATION: Sanvita Medical Corporation, an exciting new medical device company in diabetes healthcare operating within one of Nova Biomedical’s facilities, is hiring a Manufacturing Engineer to provide technical support for a new line of medical devices. Working in a small and highly driven team, you will have an opportunity to learn and grow, while contributing to a wide range of projects and assignments, including: Update and create all forms of manufacturing documentation conform to Quality System Regulations (QSR’s) and ISO Standards. Write and/or execute Installation Qualifications (IQ), Operational Qualifications (OQ), Performance Qualifications (PQ), Validations, Design of Experiment (DOE), Process Failure Mode Effects Analysis (PFMEA), Process Master Validation Plans and Continuous Improvement studies/evaluations. Provide day to day technical floor support by investigation and resolution of issues that arise during the manufacturing process. etc. | 10/31/2020 |
| 324 | Nova Biomedical Waltham, MA Reagent Test Assistant Unspecified Exp: 0-2 years |
The Reagent Test Assistant will perform testing of various calibrators, controls, and additional reagents required to support company produced and OEM analyzers, by means of verbal and/or written instruction under the supervision of the Group Leader/Supervisor. Train in the setting up, qualification, operation and troubleshooting of various analyzers and lab equipment. Record and report results as to whether the reagent/control has met specification to the Group Leader/Supervisor of Test lab. Train in performing titrations, pH measurements, flame photometry, microbial culture test and viscosity. Assist in cleaning of Test Lab to ensure work area is neat and safe. Read, write and able to follow instructions in English. etc. | 10/31/2020 |
| 325 | Nova Biomedical Waltham, MA Formulation Operator - Second Shift HS diploma or equivalent Exp: 0-2 years |
The Formulation Operator will work on our Second Shift and perform batch processing of various calibrators, controls, and additional reagents required to support company produced and OEM analyzers. Essential Responsibilities: formulation of various solutions including staging of tanks, weighing and mixing of chemicals per assembly procedures (AP's) and final batch adjustment and transfer of solutions. Perform incoming inspection of raw chemicals upon receipt, maintenance of formulation equipment and cleaning as needed. Ability to accurately document and complete records of batch formulations. etc. | 10/31/2020 |
| 326 | Nova Biomedical Waltham, MA Formulation Operator - First Shift HS diploma or equivalent Exp: 0-2 years |
The Formulation Operator will work on our First Shift and perform batch processing of various calibrators, controls, and additional reagents required to support company produced and OEM analyzers. Essential Responsibilities: formulation of various solutions including staging of tanks, weighing and mixing of chemicals per assembly procedures (AP's) and final batch adjustment and transfer of solutions. Perform incoming inspection of raw chemicals upon receipt, maintenance of formulation equipment and cleaning as needed. Ability to accurately document and complete records of batch formulations. etc. | 10/31/2020 |
| 327 | Nova Biomedical Waltham, MA Reagent Packager I - First Shift HS diploma or equivalent Exp: 1+ year(s) |
The Packager, under general supervision, will follow established procedures in packaging reagent kits. This individual is responsible for working on an assembly line to assemble the various kits within the established quality and time standards. The individual will work with various packaging equipment such as: automated/manual tape machines, manual pallet trucks, conveyors, flow racks and other packaging devices. | 10/31/2020 |
| 328 | Nova Biomedical Waltham, MA Replenishment Associate, Receiving HS diploma or equivalent Exp: 1+ year(s) |
The Receiving Replenishment Associate's is responsible for maintaining raw inventory within the raw material warehouse area. As part of the Receiving Team, the Replenishment Associate will be responsible for (1) the moving of raw material from the Receiving dock to the warehouse, (2) the consolidating of raw material in the warehouse, and (3) the picking and delivering of raw materials to the manufacturing floor. The Replenishment Associate will use documented procedures and good judgement to ensure inventory is stocked in an optimum manner, controlled, and ready for picking. Essential Responsibilities: Essential Responsibilities are to ensure the accurate movement (stocking, replenishing, consolidating, blocking, fulfilling) of materials and products within the Distribution Department and report any /all batch number or quantity discrepancies related to Distribution materials. etc. | 10/31/2020 |
| 329 | Novo Nordisk Clayton, NC Manufacturing Process Technician I HS diploma/AS/AA Exp: 1+ year(s) |
Operate manufacturing equipment to achieve production goals. Accountabilities: Work in a safe and environmentally responsible manner. Setup, operate, monitor and control equipment, systems and processes. Execution of production schedule to achieve production goals. Maintaining aseptic areas and performing sanitizations environmental monitoring. Actively participate in and support event response. Reviewing and authoring Standard Operating Procedures (SOP’s) and other documents as required. Assist during equipment maintenance including restoration of lost function, predictive and preventative maintenance. etc. | 11/3/2020 |
| 330 | Novo Nordisk West Lebanon, NH Quality Control Technician AS/AA Exp: 1 year |
Testing and laboratory operational support for Quality Control (QC) Good Manufacturing Practice (GMP) functions. Role focuses on support activities such as routine testing, sample and buffer preparation, laboratory inventory, waste management, material inspection, and general laboratory support. This position will be a Sunday - Thursday 8-5 p.m. schedule. Main Job Tasks: Sample receipt/login/inspection. Routine testing support as needed. Utility and cleaning sample testing via Total Organic Carbon (TOC) analyser. etc. | 11/3/2020 |
| 331 | Novo Nordisk Clayton, NC Quality Control Technician I AS/AA Exp: 1+ year(s) |
Perform & review analysis of in-process, release & stability samples of Active Pharmaceutical Ingredient (API) and/or filled product in accordance with Current Good Manufacturing Practice (cGMP), site & corporate policies & procedures. Accountabilities: Accuracy & Scientific Soundness of Lab Data. Environmental Compliance. GMP Compliance of Laboratory. Maintain testing proficiency for methods. Timeliness of Lab Results & Investigations. Operational support of the QC Laboratory. etc. | 11/3/2020 |
| 332 | Novo Nordisk Clayton, NC Filling Technician I - Day Shift HS diploma/AS/AA Exp: 1+ year(s) |
Filling of insulin and media preparations under aseptic conditions and operation of inspection equipment to achieve production goals. Accountabilities: Work in a safe and environmentally responsible manner. Operating, monitoring and controlling equipment, systems and processes associated with the Vial/Cartridge filling and inspection lines. Achieving production goals. Maintaining aseptic areas and performing sanitizations and environmental monitoring. Actively participate in and support event response. Reviewing and authoring Standard Operating Procedures (SOP’s) and other documents as required. etc. | 11/3/2020 |
| 333 | Novo Nordisk West Lebanon, NH Manufacturing Technician Nights BS Exp: Not required for BS candidates |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to Current Good Manufacturing Practices (cGMPs), established manufacturing practices and procedures, and compliance with quality regulations and guidelines. Main Job Tasks: Product manufacturing and product manufacturing support activities. Completion of routine documentation associated with the manufacture of product. Support in-process activities and product development when instructed by supervisor. etc. | 11/3/2020 |
| 334 | Novozymes Franklinton, NC Downstream Research Engineer, Global Optimization MS in chemical engineering Exp: Not necessary for MS candidates |
We’re seeking an energetic and self-directed person to join our Global Optimization Downstream team in the US. Your primary purpose is to have a focused effort on optimization of the downstream production processes to liberate capacity, reduce the variable cost, and improve product quality and robustness. You will contribute to Novozymes build-up in scientific and technical knowledge within downstream processing. In this role you’ll make an impact by: Testing improvement hypothesis at small scale and upscaling ones that prove successful. Leading projects to improve economies and capacities. Working together with Process Engineering and Operations to realize gains. etc. | 10/31/2020 |
| 335 | NuVasive Memphis, TN Associate Material Handler - Distribution 1st Shift HS diploma or equivalent Exp: 1+ year(s) |
The Distribution Coordinator initiates, maintains, and compiles records associated with ordering, receiving, storing, issuing, and shipping materials, supplies, and equipment by performing the following duties. Compares nomenclature, stock numbers, and other listed information on packing slips to verify accuracy of purchase orders and shipping orders. Compiles data from sources such as contracts, purchase orders, invoices, requisitions, and accounting reports and writes, types, or enters information into computer to maintain inventory, purchasing, shipping, and other records. Verifies inventory computations against physical count of stock and adjusts errors and reports documenting reasons for discrepancies with proposed corrective action. Compiles and maintains manual or computerized records such as material inventory, in process production reports, and status of material locations. etc. | 10/31/2020 |
| 336 | NuVasive Memphis, TN Loaner Processing Technician - Surgical Device Sets HS diploma or equivalent Exp: <1 year |
Performs the physical or administrative tasks involved in the shipping, receiving, storing, distributing and order fulfillment of merchandise, products, materials, parts, supplies and equipment. Checks goods received and for distribution against purchase orders or invoices, maintains records of goods and rejects unsatisfactory items. Packages and prepares products and merchandise for final shipment and posts weights and shipping charges. Lifts heavy items and may operate a forklift. Prepares and maintains records of merchandise shipped. Reviews customer orders, examines, stocks and distributes merchandise, products and materials in inventory warehouses, distribution centers or manufacturing lines. Initiates, maintains, and compiles records associated with ordering, receiving, storing, issuing, and shipping materials, supplies, and equipment by performing the following duties: Compares nomenclature, stock numbers, and other listed information on packing slips to verify accuracy of purchase orders and shipping orders. etc. | 10/31/2020 |
| 337 | NuVasive Portland, OR Distributor, Sales Associate (Portland/Bend) BS/BA Exp: 1+ year(s) |
The Sales Associate is responsible for providing a wide variety of field sales support within an assigned geography while developing to become a sales specialist. Essential Responsibilities: Develop the required technical, clinical and sales competencies through the completion of the sales associate development program in order to qualify and meet the expectations of becoming a Sales Specialist within 18-24 months. Provide coordination and logistic support in properly ordering, transporting, setting up and reassembling surgical instrument sets inside sterile processing departments at hospitals and surgery centers. Act as a product support consultant to surgeons and operating room staff during surgical procedures in the safe and proper use of NuVasive® products and related surgical techniques. Support and contribute to the growth of revenues in assigned Sales Specialists territories through delegated business development activities with surgeons, hospitals and related staff. etc. | 10/31/2020 |
| 338 | NuVasive Chicago, IL Sales Associate (Chicago, IL) BS/BA Exp: 1+ year(s) |
The Sales Associate is responsible for providing a wide variety of field sales support within an assigned geography while developing to become a sales specialist. Essential Responsibilities: Develop the required technical, clinical and sales competencies through the completion of the sales associate development program in order to qualify and meet the expectations of becoming a Sales Specialist within 18-24 months. Provide coordination and logistic support in properly ordering, transporting, setting up and reassembling surgical instrument sets inside sterile processing departments at hospitals and surgery centers. Act as a product support consultant to surgeons and operating room staff during surgical procedures in the safe and proper use of NuVasive® products and related surgical techniques. Support and contribute to the growth of revenues in assigned Sales Specialists territories through delegated business development activities with surgeons, hospitals and related staff. etc. | 10/31/2020 |
| 339 | NuVasive Philadelphia, PA Sales Associate (Philadelphia, PA) BS/BA Exp: 1+ year(s) |
The Sales Associate is responsible for providing a wide variety of field sales support within an assigned geography while developing to become a sales specialist. Essential Responsibilities: Develop the required technical, clinical and sales competencies through the completion of the sales associate development program in order to qualify and meet the expectations of becoming a Sales Specialist within 18-24 months. Provide coordination and logistic support in properly ordering, transporting, setting up and reassembling surgical instrument sets inside sterile processing departments at hospitals and surgery centers. Act as a product support consultant to surgeons and operating room staff during surgical procedures in the safe and proper use of NuVasive® products and related surgical techniques. Support and contribute to the growth of revenues in assigned Sales Specialists territories through delegated business development activities with surgeons, hospitals and related staff. etc. | 10/31/2020 |
| 340 | NuVasive Memphis, TN Assoc. Loaner Processing Technician HS diploma or equivalent Exp: 1+ year(s) |
Initiates, maintains, and compiles records associated with ordering, receiving, storing, issuing, and shipping materials, supplies, and equipment by performing the following duties. Compares nomenclature, stock numbers, and other listed information on packing slips to verify the accuracy of purchase orders and shipping orders. Compiles data from sources such as contracts, purchase orders, invoices, requisitions, and accounting reports and writes, types, or enters information into computer to maintain inventory, purchasing, shipping, and other records. Verifies inventory computations against physical count of stock and adjusts errors and reports documenting reasons for discrepancies with proposed corrective action. Compiles and maintains manual or computerized records such as material inventory, in-process production reports, and status of material locations. Compiles information on receipt of disbursement of material, equipment, merchandise, or supplies, and computes inventory balance, price, and cost. etc. | 10/31/2020 |
| 341 | NuVasive Memphis, TN Associate Assembler - 1st Shift HS diploma or equivalent Exp: 1+ year(s) |
The Associate Distribution Coordinator initiates, maintains, and compiles records associated with ordering, receiving, storing, issuing, and shipping materials, supplies, and equipment by performing the following duties: Compares nomenclature, stock numbers, and other listed information on packing slips to verify the accuracy of purchase orders and shipping orders. Compiles data from sources such as contracts, purchase orders, invoices, requisitions, and accounting reports and writes, types, or enters information into computer to maintain inventory, purchasing, shipping, and other records. Verifies inventory computations against physical count of stock and adjusts errors and reports documenting reasons for discrepancies with proposed corrective action. Compiles and maintains manual or computerized records such as material inventory, in-process production reports, and status of material locations. Compiles information on receipt of, disbursement of material, equipment, merchandise, or supplies, and computes inventory balance, price, and cost. etc. | 10/31/2020 |
| 342 | Omeros Seattle, WA Research Associate I, Biochemistry BS Exp: 0-2 years |
As the Research Associate I, Biochemistry, your responsibilities include: Perform a variety of routine and non-routine research assignments as supervised by a PhD scientist. Conduct routine molecular biology bench work (e.g. recombinant DNA techniques, construct generation and testing). Perform routine eukaryotic cell culture (e.g. cell passaging, viability determination and transfection). Purify recombinant protein samples from cells, using standard lysis and chromatographic techniques and characterization (e.g. SDS-PAGE, Western blotting and thermal shift assays). Keep detailed records of samples, experimental results in lab notebook and digital systems. Analyze and summarize data, present at internal meetings, and communicate regularly with managers and coworkers on experiment progress. etc. | 10/31/2020 |
| 343 | On Target Laboratories West Lafayette, IN Lab Animal Technician BS Exp: 1+ year(s) |
On Target Laboratories, Inc. discovers and develops targeted intra-operative imaging agents which illuminate malignant lesions and other diseased tissue. These imaging agents can be used by surgeons to help identify additional cancerous lesions and more precisely guide surgical oncologic procedures across a broad range of cancer types, thereby improving cancer surgery by helping to reduce the risk of recurrence and surgical complications for patients. Responsibilities: Accepts designated, business-focus projects to research, propose ideas and solutions, and present project during the weekly meetings. Conduct tumor implantations in mice. Image tumors with optical imaging agents using IVIS or Ami HT Image stations. Proficiently conduct ex vivo tissue biodistribution studies, PK studies, drug toxicity studies. etc. | 10/31/2020 |
| 344 | Ora Andover, MA Regulatory Operations Specialist I BS/BA in the applied or life sciences or communications Exp: 1 year |
The Regulatory Operations Specialist is responsible for assisting the Regulatory team in QC, document management, and submissions. This is a team and individual contributor role, reporting to the Manager of Regulatory. This position will work collaboratively with regulatory team. This position requires a strong technical background, a high degree of enthusiasm, enjoyment of working in a fast-paced environment, being self-motivated, and being able to use critical reasoning to solve problems and make decisions. etc. | 11/3/2020 |
| 345 | Ora Andover, MA Vivarium Technician BS in a life science or related Exp: 1 year |
Ora’s Vivarium Technician work in our pre-clinical in vivo labs and follow the standard operating procedures for animal care and husbandry in accordance to our IACUC protocols. The Vivarium Technician is responsible for providing enrichment, cleaning/washing housing, and feed study animals and assisting with ophthalmic animal research to support laboratory tasks for preclinical pharmacology studies, in collaboration with research associates. This work primarily includes but is not limited to animal dosing and assisting staff members with clinical observations, ophthalmic exams, ordering/receiving animal supplies, and preparing study binders. At Ora, the Vivarium Technician also supports dosing, animal handling, and data collection for study reports for the Veterinarian staff and research staff. etc. | 11/3/2020 |
| 346 | OraSure Technologies Bethlehem, PA Scientist I BS in chemistry or biology Exp: Not necessary for BS candidates |
Individual has the responsibility to work in the laboratory to help carry out specific R&D projects. Individual will work with a Sr. Scientist or a Scientist II to carry out the required lab work, help prepare reports on results, maintain laboratory notebooks according to GLPs and help prepare necessary documents for product transfer to manufacturing. This is primarily a hands-on laboratory position. Some of the work will be somewhat repetitive. Responsibilities: Doing laboratory experiments, under the direction of a Scientist II or Sr. Scientist, to develop new and improved products. Occasionally help plan experiments. etc. | 11/3/2020 |
| 347 | OraSure Technologies Bethlehem, PA Warehouse Associate I HS diploma or equivalent Exp: 1-2 year(s) |
Working under general supervision receives inbound freight and delivers materials and supplies to operating departments; prepares outbound shipments. Routinely performs additional tasks as may be required or assigned. Responsibilities: Pick, pack, and ship domestic and international orders according to quality and shipping procedures. Loads and unloads material from trucks or within a warehouse or storage facility. Receives freight and checks for damaged or defective goods. Delivers materials, supplies, and equipment to operating departments. Fill material requirements from manufacturing. etc. | 11/3/2020 |
| 348 | OraSure Technologies Bethlehem, PA Quality Control Specialist I AS in chemistry, biology, medical technology, or related Exp: 1 year |
Quality Control Specialist I personnel perform procedures that include evaluation of raw materials, in-process components, finished products, stability testing, equipment quality control, and equipment maintenance in compliance with guidelines established by Orasure Technologies and regulatory agencies. This position is on a 2nd shift M-F 2:30-11pm with training on 1st shift M-F 6:30am-3pm. Responsibilities: Perform all procedures accurately and according to written Work Instructions and SOPS as indicated in the Quality Control procedures and other applicable facility procedures. Perform testing at all levels of production including raw materials, in-process components, finished products and stability testing. Perform visual finished product inspections. etc. | 11/3/2020 |
| 349 | Pacira BioSciences San Diego, CA Microbiologist 1 BS 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. Responsibilities: Conduct routine environmental and systems monitoring of manufacturing and laboratory areas. Conduct general laboratory experimentation in compliance with the instructions provided in approved SOP’s to determine appropriate action. Follow policies and assists in the development of new procedures and/or documents. Maintain records of experiments performed and results obtained including appropriate calculations. Assist in the interpretation of data as require and conduct accurate and precise experimentation and complete. etc. | 11/3/2020 |
| 350 | Pall Pensacola, FL Operator II HS diploma or equivalent Exp: 1-2 year(s) |
A Production Operator II is proficient in the independent set-up, start-up, continuous operation and shutdown of your assigned area process or processes as detailed by your Value Stream (VS). Essential Job Duties: Set-up, start-up, continuous operation and shutdown of manufacturing equipment and processes, using adherence to Standard Work Instructions (SWIs), Good Manufacturing Practices (GMP) and current Good Documentation Practices (cGDP). Monitor Critical-to-Quality (CTQs) media metrics, e.g. Delta-P, KL, Thickness, Basis Weight, etc. through Statistical Process Control (SPC) – where applicable – to ensure the highest quality media possible. When appropriate, perform adjustments to the process using formally detailed and approved Corrective Methods (CMs). Advance any manufacturing process issues in a timely manner to minimize scrap and downtime. etc. | 11/3/2020 |
| 351 | Pall Putnam, CT Night Shift Production Operator II HS diploma or equivalent Exp: 1-2 year(s) |
An Operator II supporting our Night Shift is proficient in the set-up, start-up, continuous operation and shutdown of the assigned Value Stream manufacturing equipment and processes using adherence to Standard Work Instructions, Good Manufacturing Practices and current Good Documentation Practices. Essential Job Duties: Work overnight shift 4 days/week (includes a shift differential). Follow all practices and procedures regarding safety and quality compliance including OSHA, cGMP, ISO 9001 & ISO 14000 requirements. Find and suggest opportunities to improve when possible. Follow a weekly schedule and showcase strong attendance reliability. Read, Follow and support the training of other associates on Standard Operating Procedures. Develop proficiency of requisite manufacturing processes and most equipment through on-the-job training and be able to assist in training other associates in Value Stream. etc. | 11/3/2020 |
| 352 | Pall Pensacola, FL Production Operator II HS diploma or equivalent Exp: 1-2 year(s) |
A Production Operator II is proficient in the independent set-up, start-up, continuous operation and shutdown of your assigned area process or processes as detailed by your Value Stream (VS). Essential Job Duties: Set-up, start-up, continuous operation and shutdown of manufacturing equipment and processes, using adherence to Standard Work Instructions (SWIs), Good Manufacturing Practices (GMP) and current Good Documentation Practices (cGDP). Monitor Critical-to-Quality (CTQs) media metrics, e.g. Delta-P, KL, Thickness, Basis Weight, etc. through Statistical Process Control (SPC) – where applicable – to ensure the highest quality media possible. When appropriate, perform adjustments to the process using formally detailed and approved Corrective Methods (CMs). Advance any manufacturing process issues in a timely manner to minimize scrap and downtime. etc. | 11/3/2020 |
| 353 | Par Pharmaceutical Rochester, MI Process Engineer I MS in chemical or other engineering Exp: 1+ year(s) |
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. Process Engineering duties within a single location. Make decisions within guidelines and policies. Follow established procedures to perform assignments, with general instructions on the process and desired outcome. Work is reviewed for soundness of technical judgment and accuracy. etc. | 11/3/2020 |
| 354 | Myriad Austin, TX Research Associate I BS Exp: 0-5 years |
Plan, perform, evaluate the process of manufacturing reagents. Principal Responsibilities: Manufacture reagents required for the testing of samples, including but not limited to coupling of antibody to beads, biotinylation of antibody for detection, testing of minipool and simplex reagents, batching and qualification of new lots of batched reagents, and troubleshooting problematic reagents. Conduct assigned experiments and assists in their designs. Follow directions and laboratory procedures as assigned by supervisor. Analyze, interpret, and report results. Help to complete projects on time and within budget. Support transition of methods and reagents to customers. Serve as expert in area of specialization in relations with other scientific personnel. etc. | 10/25/2020 |
| 355 | Myriad Salt Lake City, UT Intake Associate (Remote) HS diploma or equivalent Exp: 6-12 months |
Responsibilities: Translate critical healthcare information and test orders from test request forms into database accurately and timely. Review received orders for required elements and effectively communicate missing elements. Ensure a high level of quality throughput. Complies with applicable CLIA and HIPAA regulations. etc. | 10/25/2020 |
| 356 | NAMSA Northwood, OH Animal Care Technician HS diploma or equivalent Exp: 0-2 years |
Principal Duties and Responsibilities: Primarily involved in the welfare and husbandry activities of animals, including sanitation of equipment and the vivarium. Receives, identifies, and acclimates laboratory animals. May euthanize animals. May administer medications under the direction of a Veterinarian. Follows the Quality Manual, all NAMSA SOPs, and Process documents. Documents all required tasks. May administer treatments as directed by staff veterinarian. May conduct training on husbandry tasks for other Associates and update training records. etc. | 10/25/2020 |
| 357 | NAMSA Irvine, CA Microbiology Technologist BS/BA Exp: No experience required |
Principal Duties and Responsibilities: 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. etc. | 10/25/2020 |
| 358 | NAMSA Northwood, OH Lab Technologist - In Vivo BS/BA Exp: Not necesary for BS/BA candidates |
Principal Duties and Responsibilities: May prepare all testing/test article and animals according to written instructions and protocols. May execute routine testing per NAMSA SOPs, with appropriate data analysis. May communicate test schedule updates to NAMSA management as needed. May prepare and maintain reagents and/or test articles as required for testing. Maintain ancillary records (log books, worksheets). Maintain relevant supplies and equipment used in routine testing. Routes all positive results or unusual testing occurrences to management. May be required to conduct daily health observations. May be required to administer the test article or extract according to written instructions. etc. | 10/25/2020 |
| 359 | NAMSA Northwood, OH Chemist MS/MA Exp: Not necesary for MS/MA candidates |
Principal Duties and Responsibilities: Independently conduct testing according to written instructions. May be requested to conduct more involved studies. May perform USP and EP monograph testing activities using wet chemical and analytical instrumentation. May conduct routine testing per NAMSA SOPs as well feasibility, protocol driven methodology, and/or method verifications on at least one of the following instrument types: HPLC, GC, or ICP, etc. Works with management to ensure large studies are completed on or before the due date. Prepare and maintain the reagents required for testing. May mentors and train staff in general laboratory testing as well as offering more complex instrumentation training. etc. | 10/25/2020 |
| 360 | NAMSA Irvine, CA Microbiology Technologist - Sterility Assurance BS/BA Exp: Not necesary for BS/BA candidates |
Principal Duties and Responsibilities: 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. etc. | 10/25/2020 |
| 361 | Nanomix Emeryville, CA Research Associate BS in chemistry, chemical engineering, biology, bioengineering, or related Exp: 3 months |
Design and develop new cartridge prototypes, working with biosensors, filters, conjugate pads, microfluidics, device programming, etc. to enable specific biological assays on the eLab platform. Design processes required to manufacture product components by developing fixtures (CAD, Laser Printer, 3D Printer, Solidworks etc.), installing necessary components on machinery (Vacuum, Pressure Gauge, Pressure Regulator etc.), scripting robotic liquid handlers, drafting qualification requirements, and writing quality documentations. Design and execute biological wet lab experiments using ELISA, enzymatic assays, chromogenic assays, fluorescence/chemiluminescence. Work with electrochemical (CV, chronocoulommetry) and analytical (FTIR, Raman) tools to characterize biosensors and their performance. Develop quality control methods and implement them in the quality system. etc. | 10/25/2020 |
| 362 | Nanostring Bothell, WA Kitting Associate I Unspecified Exp: 0-2 years |
The Kitting Associate I is responsible for kitting customer orders. Essential Duties: Accept receipt of products and ensure that materials are in good condition. Unpack and check goods received against purchase orders or invoices. Operate effectively in our ERP system for goods receipts and to create and process production orders and shipments. Maintain all records related to incoming goods. Reject unsatisfactory items as required, and assess the need to file claims with carrier. Participate in weekly cycle counts, and assist with reconciliation of item variance. Kitting raw materials into finished goods using Standard Operating Procedures. Process customer orders through the NAV ERP system. Verify inventory locations and availability for shipment against requirements specified in purchase orders. etc. | 10/25/2020 |
| 363 | Nanostring Seattle, WA Process Engineer II MS Exp: Not necessary for MS candidates |
Summary: The Process Engineer II is responsible for developing, implementing, and troubleshooting new methods used in manufacturing in support of the release of new products. This individual will assist in design, development, and scale-up of processes, instruments, and equipment from the laboratory through the pilot plant and manufacturing process. This individual may establish operating equipment specifications and improve manufacturing techniques. In addition, this individual is involved in new product development, process improvement, and design transfer activities, and may serve as a Process Development lead on project teams. Essential Responsibilities: Develop methods for the manufacturing and use of NanoString products. Develop and draft SOPs, Batch Records, Specifications, and other documentation associated with process transfer to a Manufacturing environment. Assist with performing and documenting Risk Assessments. Assist with design, document and summarize Verification and Validation studies. Draft protocols, experimental summary reports, quality documents and other scientific literature associated with projects. etc. | 10/25/2020 |
| 364 | Nanostring Bothell, WA Instrumentation/Calibration Tech I BS Exp: 1+ year(s) |
Summary: The Instrumentation/Calibration Tech I is responsible for the maintenance, testing, troubleshooting, calibration, and repair of a variety of circuits, components, analytical equipment, and instrumentation for laboratory and manufacturing equipment Requirements: Minimum 1 year of experience in the biotech or life sciences field Bachelor of Science degree in a relevant science or engineering related field or commensurate experience Basic computer skills (Excel, Word) and good communication skills Ability to work both as part of a team and independently Ability to lift a minimum of 50 lbs Valid Washington driver’s license. etc. | 10/25/2020 |
| 365 | Natera San Carlos, CA QC Reagent Associate I BS in biology, chemisry, or related Exp: 0-1 year(s) |
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. etc. | 10/25/2020 |
| 366 | Natera Austin , TX IQC-Reagents Associate 1 HS diploma or equivalent Exp: 1+ year(s) |
Support the activities for reagents used in the Operations Department’s Clinical Laboratories, which includes but is not limited to incoming material inspections to assure product safety and compliance to specifications, GMP’s, and ISO requirements. PRIMARY RESPONSIBILITIES: Coordinate labeling and prep for reagents following standard operating procedures with little to no errors. Receive, verify, label, store reagents according to department procedures. Responsible for ensuring reagents are stored in appropriate conditions. Ensures all dispenses are qualified and accounted for. Verify that data is properly entered into laboratory inventory system. etc. | 10/25/2020 |
| 367 | Natera San Carlos, CA Equipment Lab Technician BS/BA Exp: 0 years |
The Equipment Laboratory Technician will join the QC Equipment team in the Operations department to support the equipment used in the clinical laboratories. Responsibilities will include activities related to the maintenance of accessory equipment used in the Operations lab. PRIMARY RESPONSIBILITIES: Receive and label new equipment according to department procedures. Update and upkeep equipment inventory. Coordinate calibration schedule for all accessory equipment with appropriate in-house personnel or outside vendors. Execute and document maintenance performed on accessory equipment based on recommended intervals. Maintain calibration and maintenance records. etc. | 10/25/2020 |
| 368 | Natera Austin , TX QC Equipment Specialist I BS/BA Exp: 0-2 years |
Supports equipment and instrumentation utilized in the Operations laboratory. The QC Equipment Specialist is the primary point of contact for production lab personnel when equipment and instruments are not operating or not meeting operational specifications. PRIMARY RESPONSIBILITIES: Provide support for general lab equipment failures in the clinical lab to minimize downtime. Assist with diagnosis, service, and preventative maintenance on instrumentation. Coordinate scheduled and unscheduled maintenance activities, including calibration/preventive maintenance, with approved service provider. Act as point of contact and responsible party for scheduled and unscheduled equipment maintenance. Perform calibration checks on general laboratory equipment based on recommended intervals. Develop and execute procedures for the cleaning and maintenance of laboratory equipment. Execute qualification for new and/or returning laboratory equipment. etc. | 10/25/2020 |
| 369 | Natera San Carlos, CA Clinical Sample Associate I BS/BA Exp: 1 year |
At Natera we are pushing the limits creating exciting products and changing lives. We are seeking a highly motivated and team oriented individual to join the Scientific Operations team as a Clinical Sample Associate 1 to be a part of this exciting team! The ideal candidate must be detail-oriented and have an outstanding ability to perform routine laboratory research and development services. The Clinical Sample Associate 1 will work with a multidisciplinary team in a high-performance environment. PRIMARY RESPONSIBILITIES: You will work primarily with the R&D Scientific Operations team maintaining commercial sample operations for research use. Manage commercial samples transfer into R&D biobank. Verify eligibility for research use based on retention policies, patient opt-outs, and legal requirements. etc. | 10/25/2020 |
| 370 | Natera Austin, TX Clinical Laboratory Operator I BS/BA Exp: 0-2 years |
Assists in analyzing specimens and maintains equipment in good operating condition. PRIMARY RESPONSIBILITIES: Assist in testing of patient samples according to standard operating procedure. Meet expected performance metrics within role as applicable. Responsible for maintaining updated understanding and knowledge of methods performed in the lab. Provide guidance for new team members. Follows GLP (good laboratory practice): maintain clean and organized workspace. Completes training and other deadlines on time. Recognizes, escalates, and troubleshoot equipment malfunctions and common processing errors according to the laboratory’s standard operating procedures. Recognizes, documents, and escalates protocol deviations in lab to lead/supervisor. Communicates with team and other departments on various platforms (including via e-mail). etc. | 10/25/2020 |
| 371 | Natera San Carlos, CA Clinical Laboratory Associate I (Temporary) BS/BA Exp: 0-2 years |
Natera is currently seeking a Clinical Laboratory Associate I (Temporary) to analyze laboratory specimens following the standard methods and procedures while maintaining equipment and instruments in good operating condition by troubleshooting malfunctions as needed. PRIMARY RESPONSIBILITIES: Assists in testing of patient samples according to standard operating procedure in an efficient manner with little to no errors. Responsible for maintaining updated understanding and knowledge of methods performed in the lab. Follows GLP (good laboratory practice): maintain cleans and organized work space. Completes training and other deadlines on time. Recognizes and escalates equipment malfunctions; troubleshoots common errors on the lab floor. Recognizes, documents, and escalates protocol deviations in lab to lead/supervisor. Communicates with team and other departments (including via e-mail). Provides feedback on day-to-day schedule and tasks to lead/supervisor. etc. | 10/25/2020 |
| 372 | Natus Medical Middleton, WI Product Technician II AS/AA Exp: 1-2+ year(s) |
Primary Responsibilities for Production Technician II: Perform repetitive production work including configuring computers and hardware systems, loading, configuring and licensing of software. Perform standard production test routines using computerized and functional test equipment. Perform troubleshooting to identify the source of failures and resolve problems. Capture data, verify conformance to specifications and document results. Assist with other production assembly and stockroom work as required. Assist with engineering lab projects from time-to-time. Stay up-to-date and follow all Quality System procedures related to this job, which can affect the quality of products or services provided to our customers. etc. | 10/27/2020 |
| 373 | Natus Medical Middleton, WI Assembly Associate II HS diploma or equivalent Exp: 3-6 months |
Primary Responsibilities: Perform a variety of tasks including repetitive and non-repetitive production which may include assembly of components, kitting of parts and configuring assemblies. Conduct quality inspections on in-process materials. Complete documentation and other paperwork as part of the production process. Assist with stockroom and shipping work as required. Stay up to date and follow all Quality System procedures related to this job, which can affect the quality of products or services provided to our customers. etc. | 10/27/2020 |
| 374 | Nemera Buffalo Grove, IL Operator Technician HS diploma or equivalent Exp: 6+ months |
As a result of large organizational growth as well as the recent COVID-19 pandemic, Nemera is committed to helping our patients during this time of need. Be a part of the solution from the beginning and join our team as a Machine Operator in Buffalo Grove, IL! Open 24 hours and running on two-12 hour shifts from either 6pm-6am OR 6am-6pm on a 2-2-3 rotating schedule, both shifts are currently available. As a Machine Operator with Nemera, you'll operate assembly or injection molding equipment, solve equipment issues, and package the molded components or assembled products based on company and customer specifications. etc. | 10/27/2020 |
| 375 | NeoGenomics Ft. Myers, FL Clinical Laboratory Technologist - Flow Cytometry BS in medical technology or other chemical, physical, or biological science Exp: 1+ year(s) |
As a Clinical Laboratory Technologist - Flow Cytometry 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. Documents all corrective actions taken when test systems deviate from the laboratory’s established performance specifications. Demonstrates initiative in making suggestions to improve efficiency and productivity and provides consistent feedback. etc. | 10/27/2020 |
| 376 | NeoGenomics Carlsbad, CA Clinical Laboratory Technologist - Temporary, Covid Department BS in medical technology or other chemical, physical, or biological science Exp: 1+ year(s) |
As a Clinical Laboratory Technologist you will work under general supervision. You will be responsible for performing highly complex laboratory testing procedures involving Covid-19 patient samples. 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. Documents all corrective actions taken when test systems deviate from the laboratory’s established performance specifications. Demonstrates initiative in making suggestions to improve efficiency and productivity and provides consistent feedback. etc. | 10/27/2020 |
| 377 | NeoGenomics Ft. Myers, FL Clinical Laboratory Technologist, FISH - Friday - Monday, 10hr Shifts BS in cytogenetics or other chemical, physical, or biological science Exp: 1+ year(s) |
As a Clinical Laboratory Technologist – FISH 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. The shift for this position will be Friday - Monday days, days, 10hr Shifts. Documents all corrective actions taken when test systems deviate from the laboratory’s established performance specifications. Demonstrates initiative in making suggestions to improve efficiency and productivity and provides consistent feedback. etc. | 10/27/2020 |
| 378 | NeoGenomics Ft. Myers, FL Clinical Laboratory Technologist, FISH, Sun-Thur 8:00 am - 4:30 pm BS in cytogenetics or other chemical, physical, or biological science Exp: 1+ year(s) |
As a Clinical Laboratory Technologist – FISH 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. The shift for this position will be Sunday-Thursday 8:00 am - 4:30 pm: Documents all corrective actions taken when test systems deviate from the laboratory’s established performance specifications. Demonstrates initiative in making suggestions to improve efficiency and productivity and provides consistent feedback. etc. | 10/27/2020 |
| 379 | NeoGenomics Ft. Myers, FL Clinical Laboratory Technologist, Flow Cytometry, Mon - Fri 11:00pm - 7:30am BS in a chemical, physical, or biological science Exp: 1+ year(s) |
As a Clinical Laboratory Technologist Flow Cytometry 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. The shift for this position will be Monday - Friday 11:00pm - 7:30am. Documents all corrective actions taken when test systems deviate from the laboratory’s established performance specifications. Demonstrates initiative in making suggestions to improve efficiency and productivity and provides consistent feedback. etc. | 10/27/2020 |
| 380 | NeoGenomics Aliso Viejo, CA Histotechnologist I, Tues-Sat 9am-5:30pm AS/BS in histopathology Exp: Not necessary for AS/BS candidates |
As a Histotechnologist you will work under general direction to precisely and accurately conduct a variety of routine and specialized histology procedures. You will research, troubleshoot, and resolve histology related inquiries and problems within the laboratory. This position requires you to produce the highest quality of embedding, microtomy, tissue grossing, tissue processing, and H&E staining, special staining and equipment maintenance. etc. | 10/27/2020 |
| 381 | NeoGenomics Aliso Viejo, CA Histotechnologist, Tues-Sat 9pm-5:30am AS/BS in histopathology Exp: 1+ year(s) |
As a Histotechnologist you will work under general direction to precisely and accurately performing a variety of routine and specialized histology techniques and procedures. In this role, you will receive specimens, prepare them for testing and analysis, and perform filing to finish the case. You will research, troubleshoot, and resolve histology related inquiries and problems within the laboratory. This position requires you to produce the highest quality of embedding, microtomy, tissue grossing, tissue processing, and H&E staining, special staining and equipment maintenance. Receive specimens of tissue and ensure proper accessioning and labeling of all tissue samples. Process paperwork associated with accessioning and reporting. Prepare tissue specimens with chemicals, slicing, and mounting on glass slides for microscopic examination and analysis. etc. | 10/27/2020 |
| 382 | Nephron Pharmaceuticals West Columbia, SC Instrument Specialist/Chemistry Lab BS/BA Exp: Not necessary for BS/BA candidates |
Oversees all aspects of the laboratory instrumentation in the chemistry laboratory. Assists with additional work duties or responsibilities as evident or required. Performs other duties as assigned or apparent. Relies on experience and judgment to plan and accomplish goals. Performs a variety of complicated tasks under general supervision for which creativity is expected and latitude is given. Primary Accountabilities: NOTE: The Primary Accountabilities below are intended to describe the general content of and requirements of this position and are not intended to be an exhaustive statement of duties. Incumbents may perform all or most of the primary accountabilities listed below. Specific tasks or responsibilities will be documented in the incumbents' performance objectives as outlined by the incumbents' immediate supervisor or manager. Plans, organizes, and manages preventative maintenance of laboratory equipment. Creates or modifies SOPТs, forms, logbooks, etc. as necessary to facilitate the instrumentation program. Ensures that supplies are on hand to perform routine instrument maintenance and that supplies for non-routine maintenance or troubleshooting are ordered promptly as needed. etc. | 10/27/2020 |
| 383 | Nexcelom Bioscience Lawrence, MA Sales Development Representative BS/BA in the life sciences, business, or related Exp: 1+ year(s) |
Nexcelom has an immediate opening for a Sales Development Representative [SDR] in our Lawrence, Massachusetts Headquarters. The SDR will partner with marketing and sales to grow revenue and drive in-house lead generation, appointment setting, lead qualification, remote demos and sales support to the Field Sales team. This position requires heavy outbound phone calling, qualification, consultative selling skills and tight collaboration with the Field Sales team to generate new clients and maintain the existing customer base. The SDR will be expected to manage a pipeline and report on qualification and call activity. etc. | 10/27/2020 |
| 384 | NexImmune Gaithersburg, MD Research Associate/ Senior Research Associate in Cell Biology/Immunotherapy BS/MS in immunology, biology, biochemistry, or other life science Exp: 1-3 year(s) |
The Research Associate/ Senior Research Associate in Cell Biology/Immunotherapy will act as a scientific contributor for the Preclinical Immunotherapy Department developing and optimizing a new clinical approach to adoptive T cell therapy, based upon NexImmune’s proprietary artificial Antigen Presenting Cell (aAPC) technologies. The candidate will assist in the generation and phenotypical and functional characterization of antigen-specific T cells. Laboratory skills, notebook recording/maintenance, and writing of reports in acceptable scientific format(s) are important. etc. | 10/27/2020 |
| 385 | Nitto Milford, MA Quality Control Environmental Analyst I BS in chemistry, biology, or related Exp: 0-2 years |
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. Key Job Responsibilities: Perform water sampling as required per current procedures. Perform Environmental Monitoring as required per current procedures. Initiate Alert and Action documents as required. Coordinate with contract labs as appropriate for sample pickup and material drop off. Data reporting, and maintaining water trending and environmental monitoring data charts and tables. etc. | 10/27/2020 |
| 386 | Nitto Milford, MA Quality Control Analyst I/II/III BS/MS in chemistry, biology, or related Exp: 0-7 years |
The position involves the performing of routine and non-routine analyses of raw materials, in-process materials and finished products in accordance with cGMP guidelines. The appropriately trained individual may provide training and guidance to other QC Analysts. The individual troubleshoots problems associated with methods and instruments resolving them where possible or seeking guidance/authorization where required. Key Responsibilities: Test and analyze samples in a timely manner in support of project plans in accordance to cGMP guidelines. Review analytical data for compliance with specifications and cGMP guidelines. Assist in development of experimental procedures and protocols. Develop/revise documentation such as SOP, testing procedures and material specifications. etc. | 10/27/2020 |
| 387 | Nitto Milford, MA 1st shift-Temp to Hire Manufacturing Chemist I/II HS diploma or equivalent Exp: Entry level |
Purpose of Position: Responsible for the implementation of assigned production procedures working within defined production schedules. Responsible for performing all work within company and cGMP regulatory compliance. Maintaining a safe work environment and following all site safety procedure. Participation as a member of a safety team. Performs routine, generally highly structure work. Responsible for staying current with the prescribed training curriculum specified for the job title. etc. | 10/27/2020 |
| 388 | Nkarta South San Francisco, CA Cell Therapy Associate AS/BS in a relevant science or engineering Exp: 1-3 year(s) |
Working with other members of the manufacturing team, this role supports the successful tech transfer and operational readiness processes including the GMP manufacture and release of cell therapy products. Key Responsibilities: Supports the successful tech transfer and operational readiness processes using knowledge of cGMP regulations to ensure manufacturing readiness. Supports the GMP manufacture and release of cell therapy products; follows all processes and procedures related to operations in full compliance with cGMP, CFRs, site quality systems and company policies; and promotes a culture of quality and compliance. Performs process unit and support operations described in standard operating procedures (SOPs) and batch records including: media and solution preparation, cell drug substance preparation; and drug product fill operations. Performs all tasks associated with the manufacture of commercial product following batch records and SOPs. Works as part of a small team to execute GMP runs in close collaboration with process development and quality. etc. | 10/27/2020 |
| 389 | Nordson East Providence, RI Machine Technician - 2nd shift HS diploma or equivalent Exp: 1-3 year(s) |
Machine Technician I is responsible for setting up and operating specialized automated production assembly equipment as well as setting up manual jigs and fixtures for secondary operations. Additionally, responsible for detailed record keeping for equipment and production related activities. Essential Job Duties and Responsibilities: Setup and operate automated production equipment. Setup manual jigs and fixtures for production operators. Provide training and instruction to operators on proper equipment operation. Prepare all materials in advance of setup. etc. | 10/27/2020 |
| 390 | Nordson Brooklyn Park, MN Product Development Technician Supervisor - Nordson MEDICAL AS/AA Exp: 1-3 year(s) |
The Product Development Technician Supervisor is responsible for planning and directing daily activities, in coordination with the Development team, of personnel focused on Development assembly. The supervisor supports goals and objectives according to GMP’s, SOP’s and established policies, practices, procedures, quality, and cost standards. The role focuses on continuously improving efficiencies and working cross functionally to achieve overall company objectives. Essential Job Duties and Responsibilities: Participate in Development project planning to understand upcoming Development needs, changes in schedules, current challenges, and space/equipment allocation to help establish strategies to meet team goals. etc. | 10/27/2020 |
| 391 | Nordson Brooklyn Park, MN Production Operator I HS diploma or equivalent Exp: No experience required |
Position consists of assembling and inspecting medical devices in a clean room environment while under general supervision in accordance with specific work instructions and SOPs. Assembly and inspection sometimes done under a microscope. This position requires the ability to work with small tools and assemble small components using a high degree of dexterity and accuracy. This position requires direct contact with an implantable medical device. Essential Job Duties and Responsibilities: Must be able to work under direct supervision and take work instruction from Supervisor and Leads, work cooperatively and productively within a team environment. etc. | 10/27/2020 |
| 392 | Nordson Austintown, OH Material Handler HS diploma or equivalent Exp: 1-3 month(s) |
A material handler is responsible for sequencing all WIP, driven by dispatch scheduling, at each relevant machining center to enable work center efficiency and elevate execution of OTD to 90% or greater. Essential Job Duties and Responsibilities: Offloads incoming bar stock. Moves bar stock from storage area into the manufacturing process as required. Reviews machining center daily dispatch reports for machining centers and sequences bar stock in order at the relevant machining center. Transfers bar stock from machining center to machining center to assist operator efficiency. Removes clutter from the process line areas. Removes and disposes of dunnage properly. Empties machining chip hoppers as necessary. etc. | 10/27/2020 |
| 393 | Meridian Bioscience Cincinnati, OH Senior Research Associate MS Exp: 1 year |
The immunoassay function within R&D is responsible for developing the next generation diagnostic kits for Meridian. The Senior Research Associate will support the development of a new diagnostic device as part of an assay team. Responsible for designing and executing experiments, acquiring data, drawing conclusions for discussion and recommendations. Key Duties: Supports the technical work of a project – execute experiments. Participates in brainstorming discussions and sharing ideas with the team. Presentations – present data during team meetings. Data analysis – review the data generated by a given study and draw conclusions. Documentation ownership – write protocols, reports and any other documentation needed for the support of the project. etc. | 10/20/2020 |
| 394 | Merieux NutriSciences Allentown, PA Microbiology Technician AS/AA/BS/BA Exp: 1+ year(s) (AS/AA); 0 years (BS/BA) |
Your mission will be to: Job Duties: 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. etc. | 10/20/2020 |
| 395 | Merieux NutriSciences Salida, CA Chem Tech AS/AA/BS/BA Exp: 1+ year(s) (AS/AA); 0 years (BS/BA) |
Your mission will be to: Job Duties: 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. etc. | 10/20/2020 |
| 396 | Merieux NutriSciences Crete, IL Chemist I Unspecified Exp: 1-2 year(s) |
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. This position reports to the Supervisor of Chemistry. Job Responsibilities: 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. etc. | 10/20/2020 |
| 397 | Merieux NutriSciences Crete, IL Chemist III MS Exp: 1-2 year(s) |
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. Performs high end analyses with instrumentation (GCMS, LCMS, HS-LCMS, etc.) autonomously. Utilize various instruments such as LCMS, GCMS, HPLC, ICP, ICPMS, and GC to determine concentration of desired balances in the food sample. This position has the responsibilities and authority to identify departures from the quality system or test procedures and document such observation accordance with the prescribed complaint system. etc. | 10/20/2020 |
| 398 | Merieux NutriSciences Stone Mountain, GA Microbiology Technician AS/AA/BS/BA Exp: 1+ year(s) (AS/AA); 0 years (BS/BA) |
Your mission will be to: Job Duties: 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. etc. | 10/20/2020 |
| 399 | Merieux NutriSciences Cypress, CA Microbiology Technician AS/AA/BS/BA Exp: 1+ year(s) (AS/AA); 0 years (BS/BA) |
Your mission will be to: Job Duties: 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. etc. | 10/20/2020 |
| 400 | Merieux NutriSciences Gainesville, FL Chemist AS/AA/BS/BA Exp: 1-2 year(s) |
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. Job Duties: 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. etc. | 10/20/2020 |
| 401 | Merit Medical South Jordan, UT Technician III BS/BA Exp: 1 year |
Performs non-routine technical assignments of substantial variety and complexity. ESSENTIAL FUNCTIONS PERFORMED: 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. etc. | 10/20/2020 |
| 402 | Merit Medical South Jordan, UT Molding Operator II HS diploma or equivalent Exp: 1+ year(s) |
This position is responsible for cosmetic part quality, dimensional charting, paperwork completion, and submission of molded component lots to Quality Assurance for final audit approval. ESSENTIAL FUNCTIONS PERFORMED: Performs start-up dimensions, as required. Packages and weighs the product and makes labels. Inspects parts visually and uses measuring tools; documents results and ensures compliance to drawings and specifications; performs testing of products, as required. etc. | 10/20/2020 |
| 403 | Merit Medical South Jordan, UT Production Operator IV HS diploma or equivalent Exp: 6 months |
Performs a variety of complex medical assembly and processing tasks as a production team member, including performing various technical assembly tasks. ESSENTIAL FUNCTIONS PERFORMED: Perform all processes within quality specifications while visually monitoring the machines/equipment used to ensure proper function. Ability to rotate through the assembly line, performing all production assembly operations. Performs on-line and in-process visual inspection of products to ensure it meets specifications per work order and procedure instructions. etc. | 10/20/2020 |
| 404 | Merit Medical Pearland, TX Production Operator II-Carton Assembly 2nd Shift HS diploma or equivalent Exp: 3-6 months |
Performs any of a variety of medical assembly and processing tasks as a production team member. ESSENTIAL FUNCTIONS PERFORMED: Assembles medical products on an assembly operation, performing a variety of tasks on a rotating basis. Ability to rotate through the assembly line. Performs on-line and in-process visual inspection of products to ensure specifications per work order and procedure are followed. Assists Team Leader and Technicians with product and/or machine change-overs. Ensures product assembled meets quality standards. etc. | 10/20/2020 |
| 405 | Merit Medical South Jordan, UT Production Operator III HS diploma or equivalent Exp: 3 months |
Performs a variety of medical assembly and processing tasks as a production team member, including performing various technical assembly tasks. ESSENTIAL FUNCTIONS PERFORMED: May include but not limited to performing one or more processes within quality specifications while visually monitoring the machines/equipment used to ensure proper function. Ability to rotate through the assembly line, performing all production assembly operations. Performs on-line and in-process visual inspection of products to ensure it meets specifications per work order and procedure instructions. etc. | 10/20/2020 |
| 406 | Merit Medical South Jordan, UT Production Operator III (Catheter Line) HS diploma or equivalent Exp: 3 months |
Performs a variety of medical assembly and processing tasks as a production team member, including performing various technical assembly tasks. ESSENTIAL FUNCTIONS PERFORMED: May include but not limited to performing one or more processes within quality specifications while visually monitoring the machines/equipment used to ensure proper function. Ability to rotate through the assembly line, performing all production assembly operations. Performs on-line and in-process visual inspection of products to ensure it meets specifications per work order and procedure instructions. etc. | 10/20/2020 |
| 407 | Merit Medical South Jordan, UT Production Operator IV HS diploma or equivalent Exp: 6 months |
Performs a variety of complex medical assembly and processing tasks as a production team member, including performing various technical assembly tasks. ESSENTIAL FUNCTIONS PERFORMED: Perform all processes within quality specifications while visually monitoring the machines/equipment used to ensure proper function. Ability to rotate through the assembly line, performing all production assembly operations. Performs on-line and in-process visual inspection of products to ensure it meets specifications per work order and procedure instructions. etc. | 10/20/2020 |
| 408 | MSD Rockville, MD Engineer I, Process BS in chemical or biochemical engineering Exp: 1+ year(s) |
Responsible for developing, characterizing and validating manufacturing processes to produce biochemical assay plates and related consumables. DUTIES AND RESPONSIBILITIES: Review existing manufacturing processes to determine if changes are needed to improve quality and quantity of products, reduce any variations between lots produced and expand product portfolio. Make recommendations to manager to improve/enhance processes as needed. Design and conduct process experiments on manufacturing and pilot scale equipment to determine if/how changes affect product(s) properties. In accordance with standard operating procedures, provide documentation of all experimental results and present findings to manager and other appropriate staff. etc. | 10/20/2020 |
| 409 | MSD Gaithersburg, MD Research Associate I BS in cellular and molecular biology, protein sciences, or related life science Exp: 1+ year(s) |
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. DUTIES AND RESPONSIBILITIES: Analyze and prepare reagent and product documentation, organize and procure reagents, perform experiments, analyze data and document results. etc. | 10/20/2020 |
| 410 | Microbiologics St. Cloud, MN Quality Control Lab Assistant BS/BA in microbiology or related Exp: None necessary |
Responsible for assisting Quality Control (QC) department with daily, weekly, and monthly tasks while also assisting other departments. Additional duties performed as outlined below. Responsible for labware: Preparation of labware to be autoclaved. Sterility testing. Residue checking of washed labware. Wash labware when necessary. Daily, weekly, and monthly maintenance of the laboratory equipment. Setting up QC organisms. Taking inventory and ordering of supplies. Cleaning and maintaining lab equipment, i.e. staining station, pH meter, VITEK. etc. | 10/20/2020 |
| 411 | MRI Global Gaithersburg, MD Chemist MS in chemistry, forensic science, or equivalent Exp: Not necessary for MS candidates |
MRIGlobal is seeking a highly motivated chemist to join our chemistry program in the Physical Sciences Group. The position will involve providing analytical and logistic support for US Government clients requiring characterization of unknown samples. The position will require the use of a variety of techniques for the identification of unknown materials and impurities/degradants (e.g., GC-MS, LC-MS, DART-MS, Raman, FTIR, XRF, etc.). The chemist may also be responsible for instrument calibration and maintenance, data processing and review, and assisting with drafting monthly or final reports. etc. | 10/20/2020 |
| 412 | MRI Global Kansas City, MO Microbiologist MS in biology, microbiology, molecular biology, or equivalent Exp: Not necessary for MS candidates |
MRIGlobal currently has an exciting opportunity for an Associate Scientist with emphasis in Microbiology and Molecular Biology for our Life Sciences Center in Kansas City, Missouri. With minimal supervision, this position will perform technically-based tasks and laboratory experimentation related to microbiology and molecular biology applications according to established protocols and SOPs. The individual will execute research project procedures, perform data analysis, and write summary reports. Typical methods include bacterial and viral culturing, nucleic acid extraction and PCR techniques. The individual will be responsible for proficiency in the use of all equipment and procedures for the assigned area with strict adherence to quality control and quality assurance assessments. etc. | 10/20/2020 |
| 413 | Millipore Sigma Milwaukee, WI Distribution Associate 2 HS diploma or equivalent Exp: 1+ year(s) |
The Distribution Associate role plays a critical role in the fulfillment of customer orders through the activities of receiving, picking, packing, and shipping of life science materials. Standing for long periods of time, operating powered industrial equipment and lifting up to 50lbs frequently. etc. | 10/20/2020 |
| 414 | Millipore Sigma St. Louis, MO Associate Scientist - QC Enzymes BS/AS in chemistry, biology, chemical engineering, or related life science Exp: 1+ year(s) (AS); 0 years (BS) |
At MilliporeSigma the Associate Scientist will evaluate products according to established protocols, provide technical support to others, and perform operations in support of the group and department. Safely perform operations, ensuring quality expectations are met 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. etc. | 10/20/2020 |
| 415 | Miltenyi Biotec San Jose, CA Manufacturing Associate BS in a biological science Exp: 1-3 year(s) |
As a member of the Miltenyi Biotec Manufacturing team, you will have the exciting opportunity to participate in both the manufacture and process development of T-cells and multiple other cell therapy products within a GMP environment. The unique duties of this position will primarily consist of manufacturing primary human cells including activities that involve graft engineering for cellular therapies as well as supporting the development of scalable cell culture processes. Furthermore, you will be responsible for completing successful qualifications and ongoing support procedures for clean room operations and assisting in the development, writing, and review of SOPs, material specifications, standard manufacturing procedures, batch records and other GMP documentation. Overall, your keen ability to carry out key cell processing and manufacturing procedures will champion the continued development of Miltenyi Biotec products and growing success. etc. | 10/20/2020 |
| 416 | Miltenyi Biotec Waltham, MA Molecular Biology Research Associate - Next Generation Sequencing BS in chemistry, molecular biology, biochemistry, or related Exp: 1 year |
As a member of the Miltenyi Biotec Next Generation Sequencing (NGS) team, you will be responsible for preparing sequencing chemistry reagents for the NGS team and help with instrument set up and runs. Additionally, you will work collaboratively with the leads of the amplification, nucleotide and chemistry teams, preparing sequencing chemistry reagents for experiments in the Waltham lab, organize reagent shipments to internal teams, and set-up and run sequencing instruments. As a result of your close collaboration and expertise in preparing sequencing chemistry agents, you will support the continued success of Miltenyi Biotec as a whole. etc. | 10/20/2020 |
| 417 | Minnetronix Medical St. Paul, MN Software Engineer I BS in computer science, software engineering, or similar Exp: 0-3 years |
As a Software Engineer I at Minnetronix, you’ll design, implement and test real-time embedded medical device software and supporting applications and prototypes. Working under close engineering supervision on a cross-functional team, you’ll help bring medical devices from concept through development and into production . We have a broad client base so project assignments will span an array of products, be broad in nature, and require creativity and ingenuity. Essential Duties and Responsibilities: Assist in definition, analysis and allocation of requirements. Implement source code that meets product requirements in compliance with applicable coding standards. Contribute to analysis, review and evaluation of design alternatives and failure mode analyses. Assist in the creation and document ation of module-level software architecture and all aspects of software design. Unit test source code using IDE’s, debuggers, emulators, communication analyzers, scopes, and logic analyzers. Install, qualify, and configure development tools and utilities. etc. | 10/20/2020 |
| 418 | Minnetronix Medical St. Paul, MN Software Technician I AS/AA Exp: 1-4 year(s) |
As a Software Technician I at Minnetronix, you’ll assist in the development or manufacture of products, fixtures, or prototypes while supporting the creation of new Class II/III medical devices. Working with project leaders, engineers, and other technicians, you’ll provide software engineering support. This may comprise building, testing, and qualifying tools, fixtures and prototype assemblies that include software and hardware and performing other tasks as needed. You will be expected to contribute to the team while enhancing your own technical expertise and increasing your responsibilities. We have a broad client base so project assignments will span an array of products of moderate complexity, be broad in nature, and require creativity and innovation towards self-determined, self-directed solutions. Job Duties and Responsibilities: Work in compliance with the Minnetronix Quality Management System. Embedded design support. Software tool creation, qualification, maintenance, use, and support potentially including, but not limited to: Work with software engineers to determine SW tool needs. Create and/or assimilate tools as needed. etc. | 10/20/2020 |
| 419 | Miromatix Eden Prairie, MN R&D Operations Technician -Temporary Position HS diploma or equivalent Exp: 1-2 year(s) |
Miromatrix has an immediate opening for a highly motivated R&D Operations Technician at our Eden Prairie, MN facility. The term of the position is 6 months based upon a critical business need, with the potential to advance to a full-time role based upon performance during the term of employment. Primary duties include: Performs various support functions using proper procedures to meet cGMP cleaning requirements. Maintains and cleans equipment and the facility; maintains and restocks supplies; strong attention to detail is essential while dealing with multiple tasks. Additional cleaning (i.e., emergency cleanups, construction cleanups, and room set-ups) will need to be performed on an as needed basis. Major responsibilities are preparing, maintaining, and sterilizing supplies and equipment for use in the laboratory. etc. | 10/20/2020 |
| 420 | Moderna Bloomington, IN Specialist / Engineer II, External Manufacturing, US MS Exp: 0-2 year(s) |
Reporting to the Senior Manager of US External Manufacturing, the Specialist/ Engineer II will be part of a team responsible for Moderna’s manufacturing activities at 3rd-party contract manufacturing organizations (CMO). Here’s What You’ll Do: Ensure operational and technology transfer activities are performed completely and compliantly at CMOs to deliver a quality product and meet Moderna requirements. Ensure externally manufactured drug products are produced and stored according to the appropriate documentation in order to obtain the required quality. Review instructions relating to external production operations and ensure their strict implementation by the CMOs. Ensure in collaboration with quality that the appropriate qualification, maintenance, trainings and validations are performed to meet the appropriate Moderna’s requirements. etc. | 10/20/2020 |
| 421 | Moderna Norwood, MA (Contract) Manufacturing Associate I, 1st Shift BS in biology, chemistry, chemical engineering, or related Exp: Not necessary for BS candidates |
The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based medicines for evaluation in human clinical trials. He/she will apply existing and new knowledge of bioprocess unit operations and cGMPs to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations. The successful candidate will be able to document and communicate their technical and operational observations clearly and efficiently. They will be able to operate pilot-scale bioprocessing equipment and interact fluidly with peers and supervisors in Manufacturing, and cross-functionally with Quality Control, Quality Assurance, Logistical and Process Development Technology Transfer counterparts. The anticipated time frame for this assignment is six months. etc. | 10/20/2020 |
| 422 | Moderna Norwood, MA (Contract) Manufacturing Associate I, DNA Plasmid BA/BS/AA/AS Exp: Not required |
The individual in this role will be part of a cohesive team responsible for supporting GMP DNA-based medicines for evaluation in human clinical trials focusing primarily in DNA Plasmid manufacturing. He/she will apply existing and new knowledge of bioprocess unit operations and cGMPs to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations. The successful candidate will be able to document and communicate their technical and operational observations clearly and efficiently. They will be able to operate pilot-scale bioprocessing equipment and interact fluidly with peers and supervisors in Manufacturing, and cross-functionally with Quality Control, Quality Assurance, Logistical and Process Development Technology Transfer counterparts. The anticipated time frame for this assignment is six months. etc. | 10/20/2020 |
| 423 | Moderna Norwood, MA Research Associate/Sr. Research Associate, Process Development BS in chemical engineering, chemistry, biochemistry, or related Exp: 0-3 years |
The incumbent will collaborate closely with Moderna’s process development, analytical development, and process automation teams. 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, and will be able to contribute to both process development and automation related activities. Previous experience with enzymatic reactions, chromatography, and/or tangential flow filtration is preferred. We seek applicants that are proactive, enthusiastic, and show a passion for process development. Applicants should have exceptional time management and communications skills with a strong attention to detail. etc. | 10/20/2020 |
| 424 | Moderna Norwood, MA Technician I (Material Handler) Manufacturing, 3rd Shift HS diploma or equivalent Exp: 1+ year(s) |
The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based medicines for evaluation in human clinical trials. He/she will support the handling and processing of materials within manufacturing operations at the Moderna Norward facility in accordance with established processes and procedures. The successful candidate will be able to document and communicate their operational observations clearly and efficiently. They will be curious to learn and able to demonstrate a high degree of working flexibly. Here’s What You’ll Do: Safely transport product, equipment and materials (buffers, drug substance) from the warehouse to designated areas in accordance with Standard Operating Procedures (SOP) and EH&S requirements in support of the manufacture of mRNA medicines. etc. | 10/20/2020 |
| 425 | Moderna Norwood, MA Technician I (Material Handler) Manufacturing, 2nd Shift HS diploma or equivalent Exp: 1+ year(s) |
The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based medicines for evaluation in human clinical trials. He/she will support the handling and processing of materials within manufacturing operations at the Moderna Norward facility in accordance with established processes and procedures. The successful candidate will be able to document and communicate their operational observations clearly and efficiently. They will be curious to learn and able to demonstrate a high degree of working flexibly. Here’s What You’ll Do: Safely transport product, equipment and materials (buffers, drug substance) from the warehouse to designated areas in accordance with Standard Operating Procedures (SOP) and EH&S requirements in support of the manufacture of mRNA medicines. etc. | 10/20/2020 |
| 426 | Moderna Norwood, MA Technician I (Material Handler) Manufacturing, 1st shift HS diploma or equivalent Exp: 1+ year(s) |
The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based medicines for evaluation in human clinical trials. He/she will support the handling and processing of materials within manufacturing operations at the Moderna Norward facility in accordance with established processes and procedures. The successful candidate will be able to document and communicate their operational observations clearly and efficiently. They will be curious to learn and able to demonstrate a high degree of working flexibly. Here’s What You’ll Do: Safely transport product, equipment and materials (buffers, drug substance) from the warehouse to designated areas in accordance with Standard Operating Procedures (SOP) and EH&S requirements in support of the manufacture of mRNA medicines. etc. | 10/20/2020 |
| 427 | Minnesota Valley Testing Laboratories New Ulm, MN Inorganic Laboratory Technician AS in chemistry Exp: Not required for AS candidates |
The primary responsibilities include performing basic routine analysis in our Inorganic laboratory. Position is responsible for preparing reagents and solutions, setting up laboratory equipment and performing a variety of routine wet chemistry analysis. | 10/20/2020 |
| 428 | Minnesota Valley Testing Laboratories New Ulm, MN Microbiology Laboratory Technician BS/BA in food science, biology, or chemistry Exp: Not required for BS/BA candidates |
Responsible for sample transfers and preparation in the Micro lab as well as completing analysis by setting-up laboratory samples and performing routine tests to determine microbial characteristics of Salmonella, E.coli, and Listeria. Performs samples for plating and operates dilutor. | 10/20/2020 |
| 429 | Minnesota Valley Testing Laboratories New Ulm, MN Environmental Organic Laboratory Technician BS/BA in chemistry or biology Exp: Not required for BS/BA candidates |
The primary responsibilities include sample and reagent preparation, data processing and calculations through use of LIMS. Follows method and SOPs. Performs extractions on Wisconsin DRO/EPA DRO soils and waters, 608 and 8081/8082 pesticides, 8270 base/neutral acids and TCLP samples. Performs dilutions and prepares standards. Uses accelerated solvent extractor to extract appropriate soil samples. Performs maintenance on instruments. | 10/20/2020 |
| 430 | Mylan Morgantown, WV Senior Associate, Customer Relations BS/BA Exp: 0-1 year(s) |
At Mylan, each person has the ability to make a difference. From the providers who sell and market our products, to the producers who develop and manufacture them and finally to our business partners who support the providers and producers, we all have a mission critical role. Here's how this role will help: Identify and meet U.S. customer, consumer, and HCPs needs via phone, email, or fax by clarifying issues, researching and exploring answers or alternate solutions to all inquiries within set timelines for all business units. Maintaining the CRM database by logging call details accurately in accordance with department guidelines to report various trends to senior leadership. Maintaining current thorough knowledge of all business units and product portfolios, marketing campaigns, pricing, website information, PAP programs, FAQs, and other relevant programs and information to ensure One Mylan is accurately represented as a shared service. etc. | 10/20/2020 |
| 431 | Mylan Louisville, KY Professional Sales Representative, Respiratory BS/BA Exp: 1+ year(s) |
At Mylan, each person has the ability to make a difference. From the providers who sell and market our products, to the producers who develop and manufacture them and finally to our business partners who support the providers and producers, we all have a mission critical role. Here's how this role will help: Develops business plan for assigned territory that is consistent with Mylan’s sales plans, strategies and objectives. Conducts quality sales presentations to all targeted customers. Achieve quarterly sales goals within territory while adhering to all ethical sales practices and required regulations. Understands and demonstrates targeting principles. Develops pre-call planning strategy for key targets. etc. | 10/20/2020 |
| 432 | Mylan Chattanooga, TN Professional Sales Representative, Respiratory BS/BA Exp: 1+ year(s) |
At Mylan, each person has the ability to make a difference. From the providers who sell and market our products, to the producers who develop and manufacture them and finally to our business partners who support the providers and producers, we all have a mission critical role. Here's how this role will help: Develops business plan for assigned territory that is consistent with Mylan’s sales plans, strategies and objectives. Conducts quality sales presentations to all targeted customers. Achieve quarterly sales goals within territory while adhering to all ethical sales practices and required regulations. Understands and demonstrates targeting principles. Develops pre-call planning strategy for key targets. etc. | 10/20/2020 |
| 433 | Locus Biosciences Research Triangle Park, NC Research Associate BS/MS in microbiology, synthetic biology, genetic engineering, or related Exp: 6+ months |
Locus Biosciences is seeking a highly motivated and entrepreneurial applicant to join our research and development team as a full-time Research Associate. This position is well suited for those that can accomplish defined work, as well as assist in approaching and solving complex scientific problems. This individual will be responsible for assisting in the generation, production and characterization of novel antimicrobial products. The ideal candidate will be able to independently conduct general microbiological and molecular biology research, and assist in the development of our broader research goals. This individual must be able to communicate effectively in formal and informal settings and be able to work well within a team. Candidates should have prior laboratory experience and be competent at basic molecular biology techniques. etc. | 10/13/2020 |
| 434 | Locus Biosciences Research Triangle Park, NC Data Analyst BS/MS in bioinformatics, computational biology, data science, or related Exp: 6+ months |
Locus Biosciences is seeking a highly motivated and entrepreneurial applicant to join our research and development team as a full-time Data Analyst. This individual will be responsible for assisting in the generation, production and characterization of novel antimicrobial products. Primary responsibilities include maintaining and leveraging data acquired from automated and high-throughput instruments. The ideal candidate will be able to drive the automation of data acquisition from lab instruments, maintain a data warehouse, and derive meaningful insights from large datasets. This individual must be able to communicate effectively in formal and informal settings and be able to work well within a team. Candidates should have a passion for data-driven decision making and bringing life-saving therapeutics to patients. etc. | 10/13/2020 |
| 435 | Locus Biosciences Research Triangle Park, NC Translational Medicine Research Technician BS/BA Exp: 1-5 year(s) |
Locus Biosciences is seeking highly motivated applicants to join our research and development team as a full-time Research Technician within the Translational Medicine group. 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 both Development Translational Medicine as well as the Discovery group 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 dictate. The individual must be able to communicate effectively and be able to work across interdisciplinary teams. etc. | 10/13/2020 |
| 436 | LogicBio Therapeutics Lexington, MA Research Associate/Senior Research Associate, Vector Development and Operations BS in engineering, biotechnology, biology, or related science Exp: 1-3 year(s) |
LogicBio is seeking a highly motivated and scientifically rigorous individual to join our Vector Development and Operations group at either the Research Associate or Senior Research Associate level. This position will focus on developing research vector production methods, vector analytical methods and producing pre-clinical material. Primary Responsibilities: Manufactures research grade rAAV vectors utilizing suspension cell culture in shaker flasks. Executes processes for purification of rAAV utilizing various techniques such as depth filtration, centrifugation, column chromatography and TFF. Performs occasionally analytical tests such as qPCR/ddPCR, SDS-PAGE, infectivity assays. Fills out batch records, and accurately completes documentation associated with preclinical manufacturing. etc. | 10/13/2020 |
| 437 | LGC Petaluma, CA Quality Control Technician I, Swing Shift BS in chemistry, chemical engineering, pharmaceutical sciences, or related Exp: 1+ year(s) |
The Quality Control Technician I focuses 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. Areas of Responsibility: Completing analytical Quality Control activities for chemical products in accordance with established procedures. Ensuring products tested adhere to established specifications and customer requirements for product release. etc. | 10/13/2020 |
| 438 | LGC Novato, CA GMP Manufacturing Technician I - Formulation BS/BA Exp: Not necessary for BS/BA candidates |
The GMP Manufacturing Technician I position is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements as directed by the departmental supervisor, manager or director. Areas of Responsibility: To perform this job successfully, an individual must be able to perform each essential function satisfactorily. Essential Functions: Perform manufacturing activities according to written protocols, as directed by the departmental supervisor, manager or director. Maintain batch records, equipment logs and other production records as directed per company procedures. Maintain a clean an orderly laboratory environment. etc. | 10/13/2020 |
| 439 | Lumenis Salt Lake City, UT Test Technician AS/AA in laser/electro optics Exp: 1-2 year(s) |
We are seeking a highly motivated, positive and bright Technician to join our small company atmosphere with opportunities to learn and grow. This would be a rewarding, challenging and fun opportunity for the right person. Primary Function: Responsible for performing the set-up, calibration, testing, troubleshooting of circuits, components, instruments, optical and mechanical assemblies. Determines and may develop test specifications, methods and procedures from blueprints, drawings and diagrams. Tests and troubleshoots assemblies and Laser systems. etc. | 10/13/2020 |
| 440 | Luminex Austin, TX Assembly Associate I, Consumables - Limited Assignment (2nd Shift) - US AS/AA in technical electronics or a mechanical field Exp: 1+ year(s) |
The Assembly Associate I, Consumables will be responsible for: Building of cassettes for use by Engineering, Development, Clinical Studies, and product sales. Following approved cGMP manufacturing instructions and personnel are required to complete a history record of the lot built per company Quality System. Providing feedback on the processes to assure continuous improvement by noting differences in parts, assemblies, tools, fixtures, or process steps. What you will do: Coordinate with other assembly associates daily in support of integration testing, manual instruction development and production process development. All to support a quality process. Hands-on assembly, test and troubleshooting of system builds and re-work. etc. | 10/13/2020 |
| 441 | Luminex Madison, WI Manufacturing Associate I, Reagents - US AS in chemistry, life sciences, biotechnology, medical technology or related Exp: 1+ year(s) |
Delivering manufacturing requirements against production schedule within a focused manufacturing operation and/or product segment. Work schedule may include alternate shifts. Participating in manufacturing processes to support new product design transfer, stability program, process development, equipment validations, process validations and investigations and resolution of product/process issues. Performing maintenance and calibration of Manufacturing measuring and monitoring devices as well as maintaining the integrity of work areas. What you will do: Deliver manufacturing requirements and attainment of production schedule for standard inventory, build-to-order, and contract manufacture market products. Deliver manufacturing requirements for qualification/processing of incoming materials, production intermediates, and stability samples. Deliver timely and accurate completion of manufacturing sections of process documentation and related business system transactions. etc. | 10/13/2020 |
| 442 | Luminex Austin, TX Assembly Associate I, Consumables - Limited Assignment US (3rd Shift) AS/AA in technical electronics or a mechanical field Exp: 1+ year(s) |
The Assembly Associate I, Consumables will be responsible for: Building of cassettes for use by Engineering, Development, Clinical Studies, and product sales. Following approved cGMP manufacturing instructions and personnel are required to complete a history record of the lot built per company Quality System. Providing feedback on the processes to assure continuous improvement by noting differences in parts, assemblies, tools, fixtures, or process steps. What you will do: Coordinate with other assembly associates daily in support of integration testing, manual instruction development and production process development. All to support a quality process. Hands-on assembly, test and troubleshooting of system builds and re-work. etc. | 10/13/2020 |
| 443 | Luminex Austin, TX Assembly Associate I, Consumables - Limited Assignment - US (1st Shift) AS/AA in technical electronics or a mechanical field Exp: 1+ year(s) |
The Assembly Associate I, Consumables will be responsible for: Building of cassettes for use by Engineering, Development, Clinical Studies, and product sales. Following approved cGMP manufacturing instructions and personnel are required to complete a history record of the lot built per company Quality System. Providing feedback on the processes to assure continuous improvement by noting differences in parts, assemblies, tools, fixtures, or process steps. What you will do: Coordinate with other assembly associates daily in support of integration testing, manual instruction development and production process development. All to support a quality process. Hands-on assembly, test and troubleshooting of system builds and re-work. etc. | 10/13/2020 |
| 444 | Lundbeck Bothell, WA Quality Control Associate BS/BA Exp: 0-2 years |
Lundbeck is seeking a Quality Control Associate to support QC testing activities for projects in both the early and late stage of clinical and commercial development. The ideal candidate is detail oriented, organized and will have some experience in a Quality Control or other scientific laboratory or setting. ESSENTIAL FUNCTIONS: QC Sample Shipping and Sample Management. Coordinate and track sample shipments between various departments at Lundbeck and multiple CMOs/contract testing labs including international shipments. Lead a weekly multi-departmental sample shipping working group meeting. Proactively communicate shipping timelines from contract testing labs to other QC personnel and other Lundbeck contacts, as required. etc. | 10/13/2020 |
| 445 | Lygos Berkeley, CA Down Stream Processing: Lab Technician/Research Associate BS Exp: 0-3 years |
Lygos is seeking a Lab Technician/Research Associate candidate to set up, run, clean, and support downstream processing experiments. The successful candidate will have experience with general lab procedures, data interpretation and reporting in a fast paced and dynamic work environment. The candidate will work under the supervision of the Production Specialist. The candidate will be expected to work collaboratively with other team members within DSP (Down Stream Processing) and other departments including molecular biology, downstream processing, and analytical. The Lygos team works closely with all employees to support career development and facilitate the learning of new skill sets. etc. | 10/13/2020 |
| 446 | LSNE Bedford, NH QA Associate I - Document Control BS/BA Exp: 1 year |
Manage, coordinate, and maintain CGMP documentation, procedures, and records to ensure only controlled copies are reviewed, approved, issued, distributed, and archived. JOB DUTIES: Maintain Document Change Request/Quality System event databases and Master Documents/List. Maintain Designated Satellite Areas for controlled paper based record management system. Facilitate Client Batch Record Creation/Modifications/Approvals. Issue, maintain and archive Controlled Documentation/Batch Records/Testing Data Sheets/Equipment Log Books/Quality System event documents and Logs. Track and facilitate Periodic SOP reviews. Manage Record/Document Filing system. Proof and edit document changes, as necessary. Assist in client audit preparation and reconciliation. Other duties as assigned. etc. | 10/13/2020 |
| 447 | MabPlex San Diego, CA Process Development Engineer/Associate MS Exp: 1+ year(s) |
This is an intermediate experienced engineer/associate position that will play an important role in developing stable cell lines and robust cell culture processes to be used in clinical manufacturing. Experience will dictate the exact title. The position will report to the Manager of Cell Line Development. Essential Job Responsibilities: Develop stable cell lines: Host cell transfection with target plasmid. Minipool screening and single-cell cloning. Shake flask fed-batch studies to support stability studies and top clone selection. etc. | 10/13/2020 |
| 448 | Mallinckrodt Pharmaceuticals St. Louis, MO Chemistry Technician III BS in chemistry, biology, or related Exp: 1-3 year(s) |
Job Description Summary: Develop and produce pharmaceutical products via multiple methodologies, follow standard operating procedures, maintain compliance with Good Manufacturing Practices. ESSENTIAL FUNCTIONS: cGMP Active Pharmaceutical Ingredient (API) manufacturing. Conduct lab and pilot scale chemistry methods to synthesize and produce pharmaceuticals. Maintain strict FDA and cGMP compliance. Routinely and effectively maintain laboratory and supplies. Be able to troubleshoot and resolve technical issues along with comprehensive knowledge of hand tools. Follow Six Sigma and Lean manufacturing methods for stream lining and quality production. etc. | 10/13/2020 |
| 449 | Mallinckrodt Pharmaceuticals Hobart, NY Packaging Operator I HS diploma or equivalent Exp: 3-6 months |
Packaging Line Operator is responsible for tending machines and conveyors at various stages of the packaging line to maintain efficient, continuous packaging of the product for shipment. Essential Functions: Components are in Place and Filled. Sets up assigned station(s) on the line including assembly of basic equipment and preparing materials needed (e.g. bottles, caps, cotton, etc.). Tends/operates station(s) during production run to insure proper operation and keep station filled with supplies or product. Weighs product at various stages of the packaging process. Performs checks/tests required for applicable station(s). Adjusts containers/materials for proper placement and remove defective pieces. Starts and stops equipment when required. Performs hand-packaging and material-handling functions. etc. | 10/13/2020 |
| 450 | Mallinckrodt Pharmaceuticals Hobart, NY Blending Technician I - 4on/4off C Shift 6pm-6am HS diploma or equivalent Exp: 3-6 months |
Blend defined quantities of designated raw materials (per specific manufacturing instructions) into final dosage blend stage. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Blending Technician is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. Maintains accurate and compliant documentation on all activities. etc. | 10/13/2020 |
| 451 | Mallinckrodt Pharmaceuticals Hobart, NY Blending Technician I - 4on/4off D Shift 6pm-6am HS diploma or equivalent Exp: 3-6 months |
Blend defined quantities of designated raw materials (per specific manufacturing instructions) into final dosage blend stage. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Blending Technician is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. Maintains accurate and compliant documentation on all activities. etc. | 10/13/2020 |
| 452 | Mallinckrodt Pharmaceuticals Hobart, NY Blending Technician I - 4on/4off A Shift 6am-6pm HS diploma or equivalent Exp: 3-6 months |
Blend defined quantities of designated raw materials (per specific manufacturing instructions) into final dosage blend stage. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Blending Technician is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. Maintains accurate and compliant documentation on all activities. etc. | 10/13/2020 |
| 453 | Mallinckrodt Pharmaceuticals Raleigh, NC Quality Tech II BS in a physical science or related Exp: 1-3 year(s) |
The Quality Tech II analyzes process samples as received and performs non-routine analysis as requested. She/he will analyze finished goods and raw materials by chemical, physical, and instrumental means to ensure quality as needed. Must be able to work a 12 hour shift schedule of (7pm-7am) rotating shift with potential of night shift. In addition to occasional overtime as needed. ESSENTIAL FUNCTIONS: Performs in process testing for internal customers. Performs finished goods, returned goods, and stability testing for external customers as needed. Performs specified analysis on all process controls samples and reports in a timely manner by telephone or computer entry using approved written procedures and proper laboratory techniques. etc. | 10/13/2020 |
| 454 | Mallinckrodt Pharmaceuticals Hobart, NY Manufacturing Assoc I - 1st Shift HS diploma or equivalent Exp: 3-6 months |
Processes active compound materials into final tablet form performing quality control checks to maintain consistency of product according to manufacturing specifications. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Manufacturing Associate is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. Maintains accurate and compliant documentation on all activities. etc. | 10/13/2020 |
| 455 | Marker Therapeutics Houston, TX Quality Control Specialist MS in a biological science, biotechnology, or related Exp: 1 year |
The Quality Control Specialist will join a newly formed Quality Control team and report directly to Quality Control Manager. This position would give you the opportunity to be part of the brand-new Quality Control (QC) Cell Therapy Laboratory and be a key figure in day-to-day operations. The specialist will assist and collaborate with R&D on a successful transfer of analytical methods to QC. In addition to that, the QC Specialist will be performing assays in support of production, product release and stability studies on Marker’s GMP products and drug components, in accordance to the Quality Control Standard Operating Procedure and in compliance to FDA regulations. etc. | 10/13/2020 |
| 456 | Masy Bioservices Pepperell, MA Biorepository Operations Technician I HS diploma or equivalent Exp: 1-2 year(s) |
This position is responsible for storage of customer products requiring specific environmental conditions. Duties involve cleaning, couriering, shipping, receiving and inventorying. Abide by area work instructions to ensure customer product is stored appropriately and moves to/from customer and to/from Masy with appropriate controls. Accuracy, attention to detail and GMP compliance are key requirements. Duties/Responsibilities: Store product appropriately and enter information electronically into applicable system. Maintain and monitor temperature in chambers during addition and removal of product. Understand temperature and time as they relate to customer storage needs. Clean and maintain the Biorepository facility and chambers. etc. | 10/13/2020 |
| 457 | Maze Therapeutics South San Francisco, CA Research Associate II / Senior Research Associate, Stem Cell Biology (Contract) MS Exp: Not necessary for MS candidates |
We are seeking a talented and highly motivated researcher with experience in molecular and cellular biology to contribute to projects developing stem cell models for drug discovery for a variety of therapeutic areas. The successful candidate will have a thorough understanding of molecular biology with familiarity in human pluripotent stem cells (hiPSCs/hESCs). Additional experience with CRISPR gene editing, assay development, and high throughput screening is preferred. As a member of the stem cell group, you will work alongside stem cell scientists to support the growth of new differentiations, assays, and screens. This is an exciting interdisciplinary role in a dynamic cross-functional team that will contribute directly to the identification of new targets and the design and validation of novel disease-modifying therapeutics. etc. | 10/13/2020 |
| 458 | Medicomp Washington, DC Entry Level Cardiac Medical Device Sales Position - DC, VA and WV BS/BA Exp: 1-3 year(s) |
Medicomp is looking for a hard-working, charismatic, road warrior (we’ll call you an Associate Sales Manager) who is excited about playing an integral part in getting our life-saving products into the hands of the patients that need them. This might be your opportunity to break into the very desired medical device sales field. It is no secret that these jobs are hard to get and you typically need a TON of previous experience to be considered for any opportunity. Well, today is your lucky day, because we want fresh talent. We don’t want the cast-offs from other companies who are simply looking to coast and a collect bare bones paycheck. We want money motivated candidates who are system and process oriented. We want those who have a tremendous desire to rise to the top of the rankings amongst their peers. We want rock stars only! etc. | 10/13/2020 |
| 459 | Medicomp Seattle, WA Entry Level Medical Device Sales Person -Seattle BS/BA Exp: 1-3 year(s) |
Medicomp is looking for a hard-working, charismatic, road warrior (we’ll call you an Associate Sales Manager) who is excited about playing an integral part in getting our life-saving products into the hands of the patients that need them. This might be your opportunity to break into the very desired medical device sales field. It is no secret that these jobs are hard to get and you typically need a TON of previous experience to be considered for any opportunity. Well, today is your lucky day, because we want fresh talent. We don’t want the cast-offs from other companies who are simply looking to coast and a collect bare bones paycheck. We want money motivated candidates who are system and process oriented. We want those who have a tremendous desire to rise to the top of the rankings amongst their peers. We want rock stars only! etc. | 10/13/2020 |
| 460 | Medicomp San Francisco, CA Entry Level Medical Device Sales Person - NorCal BS/BA Exp: 1-3 year(s) |
Medicomp is looking for a hard-working, charismatic, road warrior (we’ll call you an Associate Sales Manager) who is excited about playing an integral part in getting our life-saving products into the hands of the patients that need them. This might be your opportunity to break into the very desired medical device sales field. It is no secret that these jobs are hard to get and you typically need a TON of previous experience to be considered for any opportunity. Well, today is your lucky day, because we want fresh talent. We don’t want the cast-offs from other companies who are simply looking to coast and a collect bare bones paycheck. We want money motivated candidates who are system and process oriented. We want those who have a tremendous desire to rise to the top of the rankings amongst their peers. We want rock stars only! etc. | 10/13/2020 |
| 461 | Medicomp New York, NY Entry Level Cardiac Medical Device Sales Position - New York BS/BA Exp: 1-3 year(s) |
Medicomp is looking for a hard-working, charismatic, road warrior (we’ll call you an Associate Sales Manager) who is excited about playing an integral part in getting our life-saving products into the hands of the patients that need them. This might be your opportunity to break into the very desired medical device sales field. It is no secret that these jobs are hard to get and you typically need a TON of previous experience to be considered for any opportunity. Well, today is your lucky day, because we want fresh talent. We don’t want the cast-offs from other companies who are simply looking to coast and a collect bare bones paycheck. We want money motivated candidates who are system and process oriented. We want those who have a tremendous desire to rise to the top of the rankings amongst their peers. We want rock stars only! etc. | 10/13/2020 |
| 462 | Medicomp Fort Lauderdale, FL Entry Level Cardiac Medical Device Sales Person - South Florida BS/BA Exp: 1-3 year(s) |
Medicomp is looking for a hard-working, charismatic, road warrior (we’ll call you an Associate Sales Manager) who is excited about playing an integral part in getting our life-saving products into the hands of the patients that need them. This might be your opportunity to break into the very desired medical device sales field. It is no secret that these jobs are hard to get and you typically need a TON of previous experience to be considered for any opportunity. Well, today is your lucky day, because we want fresh talent. We don’t want the cast-offs from other companies who are simply looking to coast and a collect bare bones paycheck. We want money motivated candidates who are system and process oriented. We want those who have a tremendous desire to rise to the top of the rankings amongst their peers. We want rock stars only! etc. | 10/13/2020 |
| 463 | Medicomp Cleveland, OH Entry Level Cardiac Medical Device Sales Position - Michigan and Ohio BS/BA Exp: 1-3 year(s) |
Medicomp is looking for a hard-working, charismatic, road warrior (we’ll call you an Associate Sales Manager) who is excited about playing an integral part in getting our life-saving products into the hands of the patients that need them. This might be your opportunity to break into the very desired medical device sales field. It is no secret that these jobs are hard to get and you typically need a TON of previous experience to be considered for any opportunity. Well, today is your lucky day, because we want fresh talent. We don’t want the cast-offs from other companies who are simply looking to coast and a collect bare bones paycheck. We want money motivated candidates who are system and process oriented. We want those who have a tremendous desire to rise to the top of the rankings amongst their peers. We want rock stars only! etc. | 10/13/2020 |
| 464 | Medicomp Melbourne, FL Digital Marketing Associate BS/BA in business, marketing, communications, or related Exp: 0-2 years |
The role of Digital Marketing Associate will be to manage Medicomp’s presence in the digital universe. This will include Facebook, LinkedIn, PPC advertising, drip campaigns, and CRM management. As the Digital Marketing Associate, you will have the opportunity to hone your SEO and advertising skills alongside a talented team of internal professionals and external consultants who live and breathe marketing. You should have a passion for digital marketing and excel at both technical- and analytical-related tasks, in addition to bringing creativity to the role. You will have a direct impact on driving lead acquisition and management efforts for our sales team by helping to execute both on our marketing plan and advertising campaigns. etc. | 10/13/2020 |
| 465 | Cantel Medical Rochester, NY Distribution Specialist - 1st Shift AS/AA Exp: 1 year |
The Specialist, Distribution is a functional role that includes distribution order picking, stocking, packaging, and other material handling and inventory control tasks to ensure timely and accurate shipments are made to our customers using various indicators or signals. To assure team continuity across all warehouse operations, this position may also be required to learn, perform, and or be certified to assist within other areas of Warehouse Operations including material & inventory, traffic, or others as assigned. The role works collaboratively with key business partners to ensure timeliness of execution, appropriate safeguards to protect during transit, and or other. Interacting with Customer Service, Purchasing, Planning, Operations and Material Control to identify and meet business requirements. etc. | 10/13/2020 |
| 466 | Cantel Medical Rochester, NY Manufacturing Support Operator HS diploma or equivalent Exp: 1-5 year(s) |
This position exists as a support to the manufacturing department. This position labels and delivers all packaging with the correct lot information and ensure that each production team member has the materials that they need to ensure maximum productivity and uptime. What you will do: Label all inner packaging with correct lot information for each machine in operation on a given shift. Apply labels to outer and intermediate packaging for all products on a given shift. Deliver materials as required to each machine in operation on a given shift. Empty the trash and scrap generated from the production cell over the course of a given shift. Assist the team lead with material movement inside the department, including raw materials, finished goods, and WIP materials. etc. | 10/13/2020 |
| 467 | Cantel Medical Rochester, NY Manufacturing Support Operator - 3rd Shift HS diploma or equivalent Exp: 1-5 year(s) |
This position exists as a support to the manufacturing department. This position labels and delivers all packaging with the correct lot information and ensure that each production team member has the materials that they need to ensure maximum productivity and uptime. What you will do: Label all inner packaging with correct lot information for each machine in operation on a given shift. Apply labels to outer and intermediate packaging for all products on a given shift. Deliver materials as required to each machine in operation on a given shift. Empty the trash and scrap generated from the production cell over the course of a given shift. Assist the team lead with material movement inside the department, including raw materials, finished goods, and WIP materials. etc. | 10/13/2020 |
| 468 | Cantel Medical Rochester, NY Manufacturing Support Operator - 2nd Shift HS diploma or equivalent Exp: 1-5 year(s) |
This position exists as a support to the manufacturing department. This position labels and delivers all packaging with the correct lot information and ensure that each production team member has the materials that they need to ensure maximum productivity and uptime. What you will do: Label all inner packaging with correct lot information for each machine in operation on a given shift. Apply labels to outer and intermediate packaging for all products on a given shift. Deliver materials as required to each machine in operation on a given shift. Empty the trash and scrap generated from the production cell over the course of a given shift. Assist the team lead with material movement inside the department, including raw materials, finished goods, and WIP materials. etc. | 10/13/2020 |
| 469 | Medpace Denver, CO Entry PC- Imaging Services BS in a health science or engineering Exp: Entry level |
Our imaging services are growing rapidly, and we are currently seeking a full-time, office-based Imaging Project Coordinator to join our team. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities: Compile and maintain project-specific status reports and project timelines associated with imaging studies; Maintain inventory of imaging supplies for study sites; and Interact with study sites and internal associates. etc. | 10/13/2020 |
| 470 | Merck Durham, NC Associate Specialist, Environmental Monitoring BS Exp: 1+ year(s) |
At least 1 year of relevant post-degree work experience in Environmental Monitoring, Aseptic Manufacturing or Microbiological Laboratory Operations. Evidence of good oral and written communication skills ( i.e., effective presentation of concepts and ideas, as well as interpersonal and conflict resolution skills). Attention to detail, flexibility and an awareness of production and attendant quality control problems. Basic understanding of GMPs and of regulatory requirements as they apply to the vaccine, sterile pharmaceutical or related fields. Ability to sit, stand and move within work-space for extended periods, ability to perform repetitive tasks including frequent hand to finger manipulations, grasping pushing and pulling; ability to lift up to 50 pounds. etc. | 10/13/2020 |
| 471 | Merck San Francisco, CA Entry Level Field Sales Representative - Women's Health (San Francisco, CA South) BA/BS Exp: Entry level |
The Women’s Health Customer Representative supports customers by providing clinical information on our Company's products, as well as education, clinical training programs, and resources. They do this to support customer needs in an effort to help the provider or system meet the goals of their patients. The Women’s Health Customer Representative is the primary point of contact for a variety of customers within their assigned geography. These customers may include: health care providers such as physicians, nurses, pharmacists as well as quality directors, LARC initiative personnel and office managers. Within their geography there are a diverse set of health care locations that they will call upon in order to execute their role including: clinics, health departments, integrated delivery systems, and hospitals. etc. | 10/13/2020 |
| 472 | Meridian Bioscience Cincinnati, OH Senior Research Associate MS Exp: 1 year |
The immunoassay function within R&D is responsible for developing the next generation diagnostic kits for Meridian. The Senior Research Associate will support the development of a new diagnostic device as part of an assay team. Responsible for designing and executing experiments, acquiring data, drawing conclusions for discussion and recommendations. Key Duties: Supports the technical work of a project – execute experiments. Participates in brainstorming discussions and sharing ideas with the team. Presentations – present data during team meetings. etc. | 10/13/2020 |
| 473 | Columbia University Irvington, NY Technician B BS Chem, Bio, Physics, related Exp: 0 yrs |
The Center for Radiological Research is seeking a technician to work with scientists studying the health hazards and antimicrobial efficacy of ultraviolet light. They will gain experience in immunohistochemistry, animal handling and husbandry, and ultraviolet exposure techniques. The primary work location will be at the Radiological Research Accelerator Facility at the Columbia University Nevis Laboratories in Irvington, NY. Occasional work at the Columbia University Irving Medical Center may be required. | 10/02/20 |
| 474 | KBI Biopharma The Woodlands, TX Manufacturing Support Associate I HS diploma/AS/AA Exp: 0+ year(s) |
The Manufacturing Support Associate I is designed as an introduction to the environment of GMP manufacturing. This position performs all routine / non routine cleanings of the GMP facilities, Process Waste, and continuously supports the manufacturing operations. This position requires a shift schedule. Aseptic and Gowning qualifications are required for this position. Must be able to document and maintain records to comply with regulatory requirements, cGMP’s, Policy Documents and SOP’s. Maintain Manufacturing facility with routine and non routine cleaning. Clean, Operate and Maintain Process Waste Area. Prepare, build and complete processing assemblies (PAR) for production. Completes Facilities response forms and ensures communication to inform other departments requiring EM sampling if required. etc. | 10/4/2020 |
| 475 | KBI Biopharma Durham, NC Research Associate BS/MS in chemistry, biochemistry, or related Exp: 0+ year(s) |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. Job Description: Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals. Makes detailed observations and carries out elementary data analysis. Understands experiments and conducts troubleshooting analysis. Maintains and updates knowledge of instrumentation. Notebook upkeep and writing skills. Maintains familiarity with current scientific literature; maintains professional expertise through familiarity with scientific literature. Assures proper labeling, handling, and storage of all chemicals used in the area; assures proper labeling and disposition of hazardous waste in satellite areas; adheres to all safety requirements and follows safe procedures, and attends all required safety and health training, including handling hazardous waste. etc. | 10/4/2020 |
| 476 | KBI Biopharma Durham, NC Research Associate I/II - Analytical Development BS/MS in chemistry, biochemistry, or related Exp: 0+ year(s) |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. Job Description: Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals. Makes detailed observations and carries out elementary data analysis. Understands experiments and conducts troubleshooting analysis. Maintains and updates knowledge of instrumentation. Notebook upkeep and writing skills. Maintains familiarity with current scientific literature; maintains professional expertise through familiarity with scientific literature. Assures proper labeling, handling, and storage of all chemicals used in the area; assures proper labeling and disposition of hazardous waste in satellite areas; adheres to all safety requirements and follows safe procedures, and attends all required safety and health training, including handling hazardous waste. etc. | 10/4/2020 |
| 477 | KBI Biopharma Durham, NC Manufacturing Associate I/II, Downstream (Days) BS/BA Exp: 0+ year(s) |
Job Summary: Coordinate and perform cGMP manufacturing operations for manufactured biopharmaceutical products. Ensure the effective use of material, equipment and personnel while making products at high quality levels. Job Description: Assist in execution of procedures for cell culture manufacturing, purification, or support area of manufacturing using SOP's and batch records. Use equipment and techniques related to support, mammalian cell culture and/or harvest and purification. Responsible for completing paperwork for each task, cleaning procedures, aseptic processing techniques, Good Manufacturing Practices (GMP) and laboratory safety practices and procedures. etc. | 10/4/2020 |
| 478 | KBI Biopharma Durham, NC Manufacturing Associate/Sr. Manufacturing Associate-Downstream (day shift) BS/BA Exp: 0+ year(s) |
Job Summary: Coordinate and perform cGMP manufacturing operations for manufactured biopharmaceutical products. Ensure the effective use of material, equipment and personnel while making products at high quality levels. Job Description: Assist in execution of procedures for cell culture manufacturing, purification, or support area of manufacturing using SOP's and batch records. Use equipment and techniques related to support, mammalian cell culture and/or harvest and purification. Responsible for completing paperwork for each task, cleaning procedures, aseptic processing techniques, Good Manufacturing Practices (GMP) and laboratory safety practices and procedures. etc. | 10/4/2020 |
| 479 | KBI Biopharma Durham, NC Manufacturing Associate/Sr. Manufacturing Associate-Upstream (night Shift) BS/BA Exp: 0+ year(s) |
Responsible for a wide variety of cell-related functions, including producing cells, intermediate product, and manufacturing final product for commercial distribution. Follow SOPs, perform daily tasks in a clean-room, retain records and write reports. May also be responsible for troubleshooting. Job Description: Assist in execution of procedures for cell culture manufacturing, purification, or support area of manufacturing using SOP’s and batch records. Responsible for various duties that are required to produce product including but not limited to cell expansion; cell feeding, harvesting, counting and freezing; product seeding; growth system maintenance; labeling, packaging and freezing of product; and culture media preparation. Follow specific techniques and operations while demonstrating an understanding of cGMPs and how they apply to specific responsibilities. Use equipment and techniques related to support, mammalian cell culture and/or harvest and purification. Responsible for completing paperwork for each task, cleaning procedures, aseptic processing techniques, Good Manufacturing Practices (GMP) and laboratory safety practices and procedures. etc. | 10/4/2020 |
| 480 | KBI Biopharma Durham, NC Research Associate/Sr. Research Associate BS/BA Exp: 0+ year(s) |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. Job Description: Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals. Makes detailed observations and carries out elementary data analysis. Understands experiments and conducts troubleshooting analysis. Maintains and updates knowledge of instrumentation. Notebook upkeep and writing skills. Maintains familiarity with current scientific literature; maintains professional expertise through familiarity with scientific literature. Assures proper labeling, handling, and storage of all chemicals used in the area; assures proper labeling and disposition of hazardous waste in satellite areas; adheres to all safety requirements and follows safe procedures, and attends all required safety and health training, including handling hazardous waste. etc. | 10/4/2020 |
| 481 | KCAS Bioanalytical & Biomarker Services Shawnee, KS Analyst I, Pharma Services BS/BA in chemistry, biochemistry, or related Exp: 1+ year(s) |
The Analyst I is responsible for preparation of reagents and solutions as well as sample processing under required regulatory documentation. Analyzes data, interprets results, and contributes to troubleshooting activities, such inventory of chemicals, washing glassware, waste disposal and/or general cleanup. May provide basic training for other laboratory personnel. Process and/or analyze samples. Prepare and label laboratory solutions. Perform and/or verify calculations related to reagent preparation and/or sample analysis. Conduct sample inventory and verify sample identities. Review information and documentation for accuracy. Prepare study records for archive. Independently create basic experiment plans. etc. | 10/4/2020 |
| 482 | KCAS Bioanalytical & Biomarker Services Shawnee, KS Laboratory Maintenance Technician BS/BA Exp: 1 year |
The Lab Maintenance Technician I performs maintenance, testing, troubleshooting, calibration and repair on support and laboratory systems. May also analyze data, interpret results or contribute to troubleshooting activities. Works on assignments that are moderately complex in nature in which judgment is required in resolving problems and making routine recommendations. ESSENTIAL FUNCTIONS: Process new and/or retired equipment. Perform calibration, repair, and preventive maintenance on support systems and laboratory equipment. Perform and/or verify calculations related to calibration and/or maintenance events. Review information and documentation for accuracy. Support the recertification of support systems and laboratory equipment. Supports activities of the Operations Department, as assigned. etc. | 10/4/2020 |
| 483 | KCAS Bioanalytical & Biomarker Services Shawnee, KS Analyst II, Pharma Services BS/BA in chemistry, biochemistry, or related Exp: 1+ year(s) |
The Analyst II is responsible for preparation of reagents and solutions as well as sample processing under required regulatory documentation. Analyzes data, interprets results, and contributes to troubleshooting activities, such inventory of chemicals, washing glassware, waste disposal and/or general cleanup. May provide basic training for other laboratory personnel. Process and/or analyze samples. Prepare and label laboratory solutions. Perform and/or verify calculations related to reagent preparation and/or sample analysis. Conduct sample inventory and verify sample identities. Review information and documentation for accuracy. Prepare study records for archive. Independently create basic experiment plans. Process and summarize data using applicable software. etc. | 10/4/2020 |
| 484 | KCAS Bioanalytical & Biomarker Services Shawnee, KS Analyst II, Pharma Dose Formulation Analysis BS in chemistry, biochemistry, biology or related Exp: 1-2 year(s) |
Responsible for preparation of reagents and solutions as well as sample processing under required regulatory documentation. Analyzes data, interprets results, and contributes to troubleshooting activities, such inventory of chemicals, washing glassware, waste disposal and/or general cleanup. May provide basic training for other laboratory personnel. Key Job Responsibilities: Typical responsibilities of the Analyst II may include, but are not limited to, the following: Process and/or analyze samples. Prepare and label laboratory solutions. Perform and/or verify calculations related to reagent preparation and/or sample analysis. Conduct sample inventory and verify sample identities. etc. | 10/4/2020 |
| 485 | KCAS Bioanalytical & Biomarker Services Shawnee, KS Report Analyst I HS diploma or equivalent Exp: Entry level |
Provide administrative support related to writing reports, test procedures, filing, and preparation of studies for archival. Works on assignments that are complex in nature in which considerable judgment and initiative are required in resolving problems and making recommendations. ESSENTIAL FUNCTIONS: Works in conjunction with Management/PSI and Quality to ensure report writing process is accurate and completed in a timely manner. Provides support for creation of reports, tables, and transmittals to be published by Management/PSI. Prepares studies for archival based on scientific department requirements. etc. | 10/4/2020 |
| 486 | KCAS Bioanalytical & Biomarker Services Shawnee, KS Analyst I, Pharma Discovery BS/AS in chemistry, biochemistry, or related Exp: Entry level |
Depending on prior experience, the Analyst I will be responsible for sample preparation/extraction, preparation of reagents and solutions under required regulatory documentation, analysis of data, interpretation of results, contributing to troubleshooting activities, performing chemical inventory, and general laboratory activities such as washing glassware, waste disposal and/or general cleanup. Once fully trained, the Analyst may provide basic training for other laboratory personnel. With demonstrated progress and initiative, the candidate will also have opportunities for learning value added skills. Key Job Responsibilities: Typical responsibilities may include, but are not limited to, the following: Process and/or analyze samples of various biological matrices. Prepare and label laboratory solutions or buffers. etc. | 10/4/2020 |
| 487 | KCAS Bioanalytical & Biomarker Services Shawnee, KS Analyst II, Pharma LC-MS/MS (2nd Shift) BS/BA in chemistry, biochemistry, or related Exp: Not necessary for BS/BA candidates |
The Analyst II will be responsible to help extend our active hours by working a 2nd shift. Primary duties are preparation of reagents and solutions under required regulatory documentation, initiating and finishing sample analysis, monitoring results, contributing to troubleshooting activities. Other duties may include performing chemical inventory, and general laboratory activities such as washing glassware, waste disposal and/or general cleanup. With demonstrated progress and initiative, the candidate will also have opportunities for learning other value-added skills. Key Job Responsibilities: Typical responsibilities may include, but are not limited to, the following: Prepare and label laboratory solutions or buffers. Perform and/or verify calculations related to reagent preparation and/or sample analysis. etc. | 10/4/2020 |
| 488 | Kite Santa Monica, CA Process Engineer, Process Technology and Materials Development MS/MA Exp: 0+ year(s) |
As a Process Engineer I, you will be responsible for designing and executing engineering activities and lab studies in support of process automation, technology development, technology evaluation, equipment qualification, process validation, and GMP manufacturing. Additional responsibilities include analyzing and presenting experimental results, drafting / reviewing protocols, production procedures, and technical reports including documentation for regulatory filings. You will work within the process technology and materials development team to design and scale-out cell therapy processes, evaluate new materials, implement innovative solutions, and support or improve existing technologies to advance Kite’s product portfolio. You will work closely with analytical, process design, validation, manufacturing sciences, operations, business strategy, and external collaborators as needed to achieve the above objectives. etc. | 10/4/2020 |
| 489 | Kite Emeryville, CA Senior Research Associate – In Vivo Unspecified Exp: 1-5 year(s) |
The in vivo pharmacology group is seeking an experienced and motivated Research Associate to join the growing team in Kite Emeryville. The candidate will join an established group, playing a key role in generating in vivo data in support of multiple programs utilizing engineered human T cells with chimeric antigen receptors (CARs). Responsibilities will include, but are not limited to: Perform in vivo studies to evaluate the efficacy of engineered T cells in mouse tumor models. Establish tumor models through SQ or IV inoculation, administer T cells IV, and dose mice with multiple agents IP or PO. Monitor in-life study measurements (tumor volume/burden, body weight), and enter data in associated software programs. etc. | 10/4/2020 |
| 490 | Kite Santa Monica, CA Research Associate, Process Design BS in biochemical engineering, chemical engineering, or related Exp: 1+ year(s) |
As a Research Associate in Process Design, you will provide process development support for New INDs, technology transfers, process validations and GMP manufacturing for Kite’s engineered autologous T cell therapy products. Additionally, you will draft and review protocols, production procedures, and process development reports. You will work with the Process Development team to design and scale-out cell therapy processes, manage equipment qualification and support process validation, as well as draft documentation for regulatory filings to advance Kite’s product portfolio. Key responsibilities: Hands on execute and collaborate on process design laboratory studies to support process development, optimization and characterization and essential process improvements. Perform hands on work in a cell culture lab and process training for GMP clinical production. etc. | 10/4/2020 |
| 491 | Krystal Biotech Pittsburgh, PA GMP Manufacturing Associate BS/BA Exp: 1+ year(s) |
Krystal Biotech, Inc is seeking a highly motivated and dynamic GMP Manufacturing Associate to support launch of and manufacturing at our Pittsburgh GMP facility. The ideal candidate will have foundation experience in upstream and/or downstream biologics or gene therapy manufacturing. Responsibilities will include, but are not limited to, the following: Develop and execute SOPs. Execute and report IQ/OQ for equipment. Operate and maintain manufacturing equipment. Perform process for manufacturing drug product for clinical trials. Clean and maintain GMP facility. Engage with process development team for tech transfer of improvements/scale up. etc. | 10/4/2020 |
| 492 | KSQ Therapeutics Cambridge, MA Scientist/Sr Scientist, Pharmacology MS Exp: 1-3+ year(s) |
KSQ Therapeutics, Inc. is seeking an exceptional and highly motivated Senior Associate Scientist/Scientist to join the Pharmacology group. The successful applicant will contribute to in vivo pharmacology efforts to support the advancement of our pre-clinical Oncology and Immuno-Oncology small and large molecule pipeline. This is a unique opportunity to learn and develop in a highly dynamic and interdisciplinary environment. Responsibilities: Independently execute on a wide variety of in vivo techniques across multiple projects with delivery of high quality data. Work collaboratively within department and across departments to effectively achieve project goals and timelines. Work enthusiastically as part of an interdisciplinary team. etc. | 10/4/2020 |
| 493 | KVK Tech Newtown, PA Packaging Supervisor AS/BS Exp: 1-3 year(s) |
Lead, train, and direct the daily activities of the Packaging/Manufacturing Departments by following all applicable Standard Operating Procedures/cGMP’s as well as maintain a safe work environment. Key Duties & Responsibilities: Supervise day to day operations of Manufacturing/Packaging. Assist with daily planning and scheduling to ensure proper workflow. Monitor, organize, and execute all functions associated with packaging of pharmaceutical commercial products and assuring compliance with cGMP, SOP, FDA, DEA, and OSHA rules and regulations. Work directly with management and group leaders to ensure appropriate follow through of the weekly planning schedule. etc. | 10/4/2020 |
| 494 | KVK Tech Newtown, PA Sample Management Associate AS/BS in a laboratory science Exp: None needed |
Sample Management Associate provides support to Sample Coordinator and performs administrative tasks in the Sample Management Department. Follows SOPs, and fulfills laboratory requests with minimum direct supervision. JOB RESPONSIBILITIES: Performs duties and training to acquire the skills required for sample and standard handling in support of the laboratory. Handling of samples received in Quality Control Laboratory. Follows SOPs, and fulfills laboratory requests with minimum direct supervision. Quality Control related tasks like receiving, documenting, distributing and reconciliation of all samples received in the laboratory. etc. | 10/4/2020 |
| 495 | KVK Tech Newtown, PA Manufacturing Operator HS diploma or equivalent Exp: 1-3 year(s) |
Operators are responsible for operating special purpose machines or industrial equipment to specifications on production basis in typical oral solid dose pharmaceutical manufacturing. Processes include dispensing and weighing of materials, using automatic and semi-automatic equipment for tablet manufacturing, combining materials to make blends and solutions, and packaging of finished product. JOB RESPONSIBILITIES: Ensure the proper set-up and operation of standard pharmaceutical process equipment such as Granulators, Blenders, Mills, Tablet Presses, Tablet Coaters and Packaging. etc. | 10/4/2020 |
| 496 | KVK Tech Langhorne, PA Quality Control Microbiologist BS in microbiology or related Exp: 1 year |
Executes the activities of QC Microbiology Laboratory by following approved microbiological and chemical test procedures and ensure their delivery in an accurate and timely manner following proper safety precautions. Also provide QC microbiology support to the Aseptic Manufacturing and validation process. DUTIES & RESPONSIBILITIES: Familiar with Drug Regulations, Pharmacopeia’s and Regulatory requirements. Authoring SOP’s and Test Methods when required. Assurance of cGMP and GLP compliance in the QC Microbiology Laboratory. Responsible for laboratory cleanliness and biohazard removal. etc. | 10/4/2020 |
| 497 | KVK Tech Newtown, PA QC Document Reviewer BS in chemistry or related Exp: 1+ year(s) |
The QC Data Review Specialist 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. JOB RESPONSIBILITIES: Daily activities include review of documentation generated during method development, method validation, stability testing, routine testing and other analyses. The individual will interface with their supervisor, the analytical groups and QA on a daily basis. etc. | 10/4/2020 |
| 498 | KVK Tech Newtown, PA Analytical Chemist BS/MS Exp: 1-4+ year(s) |
Perform analytical testing of raw materials, in-process materials, stability samples, finished products and product development products using different analytical techniques. JOB RESPONSIBILITIES: Operation, Calibration, Qualification, Preventive maintenance and routine trouble shooting of analytical instruments like UPLC, HPLC, GC, AAS, UV spectrophotometer, Dissolution apparatus, Laser Diffraction Particle Size analyzer, etc. Evaluate existing, develop and validate new analytical methods of drug products and drug substance as per FDA, USP and ICH guidelines by different analytical techniques. Document all performed analysis as per cGMP, USFDA and 21CFR211.194 guidelines. Follow cGMP (current Good Manufacturing Practices), GLP (Good Laboratory Practices), 21CFR211.22, 21CFR211.28 and 21CFR211.170. etc. | 10/4/2020 |
| 499 | KVK Tech Newtown, PA Topical Formulation Associate MS in chemistry, biochemistry, or pharmaceutical sciences Exp: 1-3 year(s) |
Person exhibits aptitude in assisting in the development of topical product pharmaceutical formulations, as well as meeting timelines for the department. JOB RESPONSIBILITIES: Assist in the development of broad range of topical product pharmaceutical formulations including gels, creams, solutions and ointments. Develop pharmaceutical formulations utilizing Quality by Design (QbD) and risk assessment concepts. Contribute and support the analytical efforts and interpretation of data generated from experimental batches. Write technical documents to support regulatory submissions and technical transfers. Interact cross departmentally and provide technical guidance to achieve company objectives. etc. | 10/4/2020 |
| 500 | Lab Connect Johnson City, TN Jr. Project Analyst BS/BA in accounting, finance, economics, business administration, or related Exp: 0-3 year(s) |
To provide financial support to the Senior Analyst and Project Manager as assigned. The mission of the position is to support the accurate reporting of the financial position of each project internally. Essential Functions (including but not limited to): Responsible for project set-up in an ERP system, client billing support, and other financial aspects of assigned projects. Assist in financial support to ensure the operational effectiveness of the project. Maintain all project data in the ERP system and on Sharepoint. Prepare reporting and financial analysis for the Finance team and issue findings and variances to plan. Identify and highlight potential issues related to project financial risks that impact company profitability. etc. | 10/5/2020 |
| 501 | Lab Connect Johnson City, TN Proposal Associate - Remote Opportunity BS/BA in science, business, or marketing Exp: 1-5 year(s) |
The following duties are normal for this position; however, they are not to be construed as exclusive or all-inclusive. Other duties may be required and assigned. Essential Duties and Other Responsibilities: Prepare quotations for protocols, bid requests, study revisions, and additions’ using the company’s pricing tools. Complete budget to actual reconciliations at predetermined time points over the course of awarded studies. Assist in making recommendations on desirable proposals based on established financial and operational criteria, as required. etc. | 10/5/2020 |
| 502 | Lampire Biological Laboratories Ottsville, PA Large Animal Technician Animal science degree Exp: Not necessary for degree candidates |
Care of animals including feeding, cleaning, treatment and preventive medicine. Daily production and maintaining the animal areas of the facility. Responsibilities Include (but are not limited to): Animal care AM/PM daily. Complete daily production which may include injections, bleeding, milking etc. Maintain animal living areas. Document findings and job completions in the required logs. etc. | 10/5/2020 |
| 503 | Lampire Biological Laboratories Everett, PA Small Animal Technician HS diploma/BS in a life science Exp: 1 year |
The primary responsibility of this individual is to maintain the overall health and well-being of the rabbits including cage and facility maintenance. This would include the feeding and watering of rabbits, administering treatments, as well as swapping, cleaning, disinfecting, and sanitizing all animal housing units and animal facilities. Responsibilities Include (but are not limited to): Feeding, watering, and administering treatments, including observing and reporting any signs of disease/illness and help to treat minor cases of such findings. Scraping, chipping, and dusting, animal caging units. Swapping/rotating animal. Caging units. Disassembling/assembling, cleaning, disinfecting, and sanitizing all animal caging units including feeders, water bottles, and enrichment items. etc. | 10/5/2020 |
| 504 | Lampire Biological Laboratories Everett, PA Purification Technician BS Exp: Not necessary for BS candidates |
This position will be responsible for the purification of antibodies at the Everett facility. Responsibilities Include (but are not limited to): Routine buffer preparation for all processes being performed in the department. Protein A and Protein G purification of Normal igGs and other antibodies. Write and revise Standard Operating Procedures (SOP’s) and Batch Records (BR) as needed. Assist in filing, labeling and finished product good inspection. Operate basic Laboratory and Analytical equipment. Compliance with all Standard Operating Procedures (SOP’s) in relation to Protein Purification. etc. | 10/5/2020 |
| 505 | Lannett Seymour, IN Drug Product and Stability Chemist I - 1st Shift BS in chemistry or related Exp: Not necessary for BS candidates |
This position is primarily responsible for the laboratory testing of in-process, release and stability samples for commercial drug products. Work on a team of 6 or more analysts. No direct reports. No purchase approval or budget responsibilities. Responsibilities: Perform accurate and timely analysis of in-process, release and stability samples for drug products according to current analytical procedures, SOPs, laboratory guidelines and safety requirements. Testing performed to include basic lab equipment and procedures, such as pH, Assay by HPLC, and Dissolution. Document all laboratory testing and maintain accurate and legible notebooks and records. Peer review of data, reports and notebooks. etc. | 10/5/2020 |
| 506 | Latham Biopharm Group Elkridge, MD Associate / Senior Associate / Consultant, Quality Assurance BS/BA Exp: 1-2 year(s) |
The ideal candidate must be able to work independently and have excellent interpersonal relationship skills with flexibility to adapt to fast pace environment with changing priorities. Job Duties: Provide consulting services for LBG client including, but not limited to: Evaluation and disposition of materials with the assurance that the materials were produced in conformance to all applicable policies/procedures of the Company's compliance with all governing regulations. Coordinate and/or support the preparation of procedures, processes and quality improvements. Assists in the coordination of significant quality events including fact-finding, investigation support, coordination of clinical quarantine and recovery actions. Collaboration with clients and vendors to ensure robust processing and continuous improvement. etc. | 10/5/2020 |
| 507 | LeMaitre Vascular Burlington, MA Quality Inspector - Non Exempt (Hourly) Position HS diploma Exp: 1-3 year(s) |
Complete in-process, final inspection of medical devices and review DHR and record QC Chemistry and Microbiology results. Responsibilities: Read work instructions to complete in-process and final inspections. Use a wide assortment of QC inspection instruments to assure components and devices are manufactured and are functioning in accordance to specifications. Use simple test equipment and record data and interpret its pass/fail status. etc. | 10/5/2020 |
| 508 | LeMaitre Vascular Burlington, MA Manufacturing Technician - Non Exempt (Hourly) Position HS diploma Exp: 1-3 year(s) |
The Manufacturing Technician is responsible for carefully following manufacturing instructions and adhering to applicable company quality standards and requirements to ensure the proper manufacturing of our collagen vascular graft. Responsibilities: Manufacture vascular graft products as required to support all customer, internal, clinical, and other demand. Package vascular grafts as required as per current process specifications. Maintain timely and accurate documentation of all manufacturing activities, including but not limited to device history records and inventory counts. Complete scheduled production runs in an efficient, timely manner to meet schedules. Participate in Continuous Improvement projects or events as requested. Assist with inventory counting activities as required. etc. | 10/5/2020 |
| 509 | Lifecore Chaska, MN Machine Operator I HS diploma or equivalent Exp: 6+ months |
The Machine Operator I is responsible for the setup and operation of standard packaging machinery in the packaging department. This includes working with and monitoring other packaging personnel to complete equipment set up and operation required by the department schedule. Machine Operators must comply with regulatory requirements, Good Manufacturing Practices (GMP), Standard Operating Procedures (SOP), and Manufacturing Process Records (MPR). They will perform all processes as required to fill, label, print, tray seal, pouch, final package, and inspect any Lifecore product; document completed work during packaging of final product; continually practice proper precautions and procedures when working with equipment and handling chemicals; participate in the review of batch records, procedures, and practices to help ensure the safety of all Lifecore products as well as personnel; identify and communicate quality issues to supervisor; acquire and maintain cleanroom and gowning qualification as required. etc. | 10/5/2020 |
| 510 | LifeSensors Malvern, PA Entry Level Scientist BS/MS in the biological sciences or related Exp: 0-2 year(s) |
We are seeking individuals who are passionate about research, bring out of the box thinking and take bold steps to develop innovative technologies with applications in the ubiquitin research field. Successful candidates will have basic knowledge of biochemistry and molecular biology techniques, in particular experience with protein expression and purification and cloning. Knowledge of the ubiquitin proteasome pathway is desired. etc. | 10/5/2020 |
| 511 | Ligand Durham, NC Associate Scientist - Molecular Biology BS/MS in cellular or molecular biology or related Exp: 0-2 year(s) |
Icagen’s facility in Durham, North Carolina currently has an opening for a talented scientist to join our Molecular Biology team. This is a full-time, laboratory-based position offering an opportunity to play key roles in identifying novel drug candidates and advancing drug development projects. The ideal candidate will have experience in a broad set of cellular and molecular biology techniques with a fundamental understanding of molecular biology. The successful candidate will be capable of managing multiple projects simultaneously while working as part of a core team. The work will be fast-paced and process-oriented in a dynamic environment which is predicated upon continuous improvement where everyone is encouraged to contribute to improving laboratory efficiency. etc. | 10/5/2020 |
| 512 | Lipocine Salt Lake City, UT Associate Scientist BS/MS in a life science, chemical engineering, or related Exp: 1-3 year(s) |
Associate scientist needed in the area of pharmaceutical drug delivery research. Responsibilities include conducting laboratory experiments in support of formulation and process development. Qualified candidates will possess a BS/MS in life Science, chemical engineering or related field or 1-3 years experience in a pharmaceutical or chemistry laboratory. Knowledge of laboratory practices and demonstrated skills in analytical instrumental techniques (e.g. HPLC) are preferred. Excellent communication skills needed for preparing and following standard test methods and reporting experimental results. | 10/5/2020 |
| 513 | Liquidia Morrisville, NC Contract - Associate Engineer or Senior Associate Engineer MS in engineering or technical discipline Exp: 0-1 year(s) |
The Associate Engineer / Senior Associate Engineer works within cross-functional teams to develop processes for the manufacturing of novel particles for engineered drug delivery. Specific Duties, Activities, and Responsibilities: Work with team of engineers and technicians to manufacture materials to support preclinical and clinical R&D projects. Serve as manufacturing representative for one or more R&D project teams to assist in process development activities to ensure adequate material supplies to meet project objectives. Support R&D project teams through the use of process engineering tool such process mapping, Cause and Effect Diagrams, pFMEA and basic Six Sigma tools. Assist project teams in the transition for lab scale to commercial scale manufacturing. etc. | 10/5/2020 |
| 514 | Hologic San Diego, CA Scientist 1 R&D MS in molecular biology, chemistry, biochemistry, or related Exp: 1-3 year(s) |
Hologic is seeking a Scientist 1 responsible for initiating, directing and executing scientific research and/or development strategies. Essential 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. Responsible for a sub-project within the overall project goals. Understands the sub-project goals within the context of the overall project. Independently designs and performs complex experiments, analyzes data and prepares reports for the sub-project in support of the overall project. May be asked to supervise daily work of junior level employees as preparation for a management role at the next level. Demonstrated competence in one or more of the following areas: Core Services – e.g. Microbiology skills, bioinformatics, sequencing, cloning, analytical chemistry, oligo synthesis and/or purification. etc. | 9/27/2020 |
| 515 | Hovione , NJ Process Engineer BS in chemical or other engineering or chemistry or other science Exp: 1-3 year(s) |
At Hovione, a Process Engineer's job mission is to ensure the best process engineering knowledge is applied in scaling up chemical and spray drying projects to maximize customer satisfaction ad Hovione's interests and in compliance with all Federal, State, Local and internal policies. It also includes the development of process engineering technical skills to increase the knowledge and offering on the best and state of the art technologies used in the industry. You will be responsible for: Plan and design manufacturing processes based on chemical procedures to run safely and effectively in a pilot plant/kilo lab in accordance with best known practices ensuring cGMP compliance. Contribute to the Process Hazard Analysis (PHA) of all processes under his/her responsibility and assure that all identified hazards are addressed prior to performing any activities within operations. Plan and design methods to improve efficiency in production. etc. | 9/27/2020 |
| 516 | Humacyte Research Triangle Park, NC Process Engineer I (MSAT) BS in engineering or related Exp: 0-2 years |
Position will support the development and execution of product lifecycle management and process analytics activities. This role will work closely with personnel in Process Development, Manufacturing, Engineering, Quality Assurance, and Quality Control. Primary Responsibilities: Support execution and development of the manufacturing control strategy and Process Analytics program. Acquire, analyze, and report data trends using graphical and statistical methods. Support technology transfer and process validation of products into commercial manufacturing. Author standard operating procedures, reports, and protocols. etc. | 9/27/2020 |
| 517 | Humacyte Research Triangle Park, NC Cell R&D Associate MS in cell biology, biochemistry, chemical engineering, mechanical engineering, or related Exp: 1-2 year(s) |
KEY RESPONSIBILITIES: Responsible for culture of primary human cells for purposes of cell expansion, characterization, and tissue engineering. Perform qRT-PCR to screen donor cells. Aseptic compounding and aliquoting media and buffers. Construct, launch and maintain bioreactors that are used to grow engineered vascular tissues. Perform cell-based assays. Verify process data, protocols, and manage supporting documents. Additional duties will include support of routine lab activities, equipment management, lab maintenance, preparation of experimental materials and protocols, and ensuring good documentation practices for all activities performed. Schedule flexibility required for some occasional cell culture activities needed outside of standard weekday business hours (e.g. weekend cell culture maintenance activities). etc. | 9/27/2020 |
| 518 | ICU Medical Salt Lake City, UT Equipment Operator I HS diploma or equivalent Exp: 0-1 year(s) |
A Equipment Operator I is responsible for the safe and efficient operation of simple automated assembly machines. This individual will ensure the continued operation of assembly machines through interpretation of and appropriate response to machine faults and through infrequent alignment of stations and fixtures. This individual will perform simple, repetitive tasks associated with machine operation and will operate machines that require a low level of attentiveness. The operator is also responsible for ensuring that medical devices are assembled with the highest quality possible. Essential Duties & Responsibilities: Keep work area and equipment clean. Able to read and understand procedures. Responsible for safe operation of equipment in accordance with Company standards and procedures. etc. | 9/27/2020 |
| 519 | ICU Medical Salt Lake City, UT Technician, Setup HS diploma or equivalent Exp: 1+ year(s) |
The Setup Technician supports the Production operation by setting tools and turn over to production ready for startup. The Setup Technician is required to participate in daily meetings to ensure job accuracy and priorities. Essential Duties & Responsibilities: Train with the Senior Process Technician. Train on Robotics and End of Arm Setup. Assure GMP’s, safety standards and procedures are followed per company policies. Responsible for reviewing crossover priorities and schedule with supervisor each morning. Working from molding crossover, obtain all required elements for priority job including documentation. Verify full last shot and samples of any cavities that were blocked from tool work order packet are collected, verify this represents all cavities and then have Process Tech shut down press. etc. | 9/27/2020 |
| 520 | ICU Medical Salt Lake City, UT Associate Maintenance Technician, Molding HS diploma or equivalent Exp: 0-2 years |
The Associate Molding Maintenance Technician is required to assist in the diagnose and repair of Molding Presses and all ancillary equipment. In addition, they must be able to communicate effectively with their customer, Production, and all support groups. Finally, they are required to accurately document the work performed which is crucial and required in achieving World Class Maintenance. Essential Duties & Responsibilities: Support preventive maintenance and daily repair of injection molding presses, and auxiliary equipment. Participate with set up reduction improvements of specific injection molding presses, molds and auxiliary equipment (conveyors, dryers, thermolators, etc.) through Kaizen improvement activities. Troubleshoot pneumatic, mechanical, hydraulic and electronic and/or combined systems on Injection Molding Machines and support equipment. etc. | 9/27/2020 |
| 521 | ICU Medical Salt Lake City, UT Service and Repair Technician AS/AA Exp: 0-2 years |
The Service Hub Technician is responsible for triaging devices where critical decisions are made on the PCI, repair, updating of service record, tracking labor and material as well as updating and printing of a Service Report that is returned with the repaired device. This person must interpret and edit the repair results into device tracking system (Oracle) so that the complaint is addressed, results are technically accurate and include all required elements ensuring that the customer understands the analysis/repair activity. Communicates with other Repair Technicians as required to clarify repair results. Essential Duties & Responsibilities: Will perform routine and complex work related to the repair and refurbished of medical devices. Troubleshoot and analyze customer device returns to problem solve root cause issues. May perform troubleshooting and repair of devices onsite at customer location. etc. | 9/27/2020 |
| 522 | ICU Medical Salt Lake City, UT Quality Inspector I AS/AA Exp: 6 months |
Independently performs inspections on parts, materials, and supplies received from vendors, perform in-process production inspections, and ensure products comply with quality standards prior to shipment. Issues acceptance or rejection tags based on outcome of inspections, checking with supervisor on more difficult determinations. Familiar with manufacturing environment, inspecting, testing, sampling, and sorting of products / goods being manufactured. Essential Duties & Responsibilities: Audit and monitor quality requirements in accordance with company quality assurances policies and customer specifications. Conduct inspections at First Article, in-process, in-coming and completes the final inspections. Perform accurate mechanical, physical and visual inspections of raw materials, components, and sub-assemblies as per inspection plans and specification requirements. etc. | 9/27/2020 |
| 523 | Idexx Elmhurst, IL Histology Laboratory Tech AS/BS/MS Exp: 1+ year(s) |
Histologists at IDEXX perform dissection, grossing, embedding, microtomy, special staining, and complex tissue diagnostics on veterinary samples from dogs, cats, birds, reptiles, and all other pets big and small. Are you looking to make a difference in the lives of pets? The pet owner counts on it! Who should reach out? If you have specific experience in dissection, embedding, cutting, grossing or special stains. Complex Tissue a PLUS. If you desire a role as a coordinator, lab tech, leader or trainer - you will be a contributor to a team focused on operational excellence and the sharing of best practices, our team of laboratory professionals are dedicated, driven and results-oriented. This is a laboratory, so there is potential exposure to biohazards, agents known to cause zoonotic diseases, and hazardous chemicals. etc. | 9/27/2020 |
| 524 | Idexx Memphis, TN Histology Laboratory Technician - Days AS/BS/MS Exp: 1+ year(s) |
Histologists at IDEXX perform dissection, grossing, embedding, microtomy, special staining, and complex tissue diagnostics on veterinary samples from dogs, cats, birds, reptiles, and all other pets big and small. Are you looking to make a difference in the lives of pets? The pet owner counts on it! Who should reach out? If you have specific experience in dissection, embedding, cutting, grossing or special stains. Complex Tissue a PLUS. If you desire a role as a coordinator, lab tech, leader or trainer - you will be a contributor to a team focused on operational excellence and the sharing of best practices, our team of laboratory professionals are dedicated, driven and results-oriented. This is a laboratory, so there is potential exposure to biohazards, agents known to cause zoonotic diseases, and hazardous chemicals. etc. | 9/27/2020 |
| 525 | iFyber Ithaca, NY Research Technician BS in the biological sciences Exp: 1 year |
iFyber is seeking a research technician to assist with R&D projects at the interface between chemistry, biology, and material science. iFyber serves clients in the regenerative medicine, medical device, diagnostics, and antimicrobial industries. The person in this position will support a variety of programs that will require experience and/or the ability to pick up bench skills related to microbiology and chemistry. Duties and Responsibilities: Conduct experimental tasks both independently. Follow established protocols and work with senior staff to adapt or design new protocols. Document information in laboratory notebooks and MS Word, Excel, and PowerPoint. Report results via verbal, written, and graphical communication. etc. | 9/27/2020 |
| 526 | Immucor Nocross, GA Production Support Technician HS diploma or equivalent Exp: 1-3 month(s) |
We are seeking a Production Support Technician I to provide day-to-day operations support for all manufacturing areas. Our ideal candidate must be able to adapt to changes in the daily/weekly schedule to ensure customer demands are met. This position's schedule is Tuesday – Friday from 10am – 8:30pm (shift may vary to meet business needs). Additional responsibilities include: Perform washroom activities, staging and set up bottles for production use and maintain inventory. Assemble bottle preparation, manifold assembly and other components for manufacturing use. Responsible for training on all procedures assigned, and has the ability to be cross trained to assist in other production areas or departments as needed. etc. | 9/27/2020 |
| 527 | Integer Plymouth, MN Associate Prototype Technician AS/BS Exp: 0-3 years |
The primary purpose of this role is to perform assembly and inspection operations over a range of new products and/or processes. Will support non-cyclical work which may include prototypes and pre-production lots in preparation for validation, clinical trials or transfers. Will also support multiple builds within the facility including lab and cleanroom environments. With guidance from Engineering on projects and using work procedures, this role provides support to the Engineering teams to meet various deadlines. May provide support to other team members or provide input to the Engineers on assembly, processes, and build/quality documentation. etc. | 9/27/2020 |
| 528 | Integer Brooklyn Park, MN Manufacturing Team Member HS diploma or equivalent Exp: 1+ year(s) |
The primary purpose of this position is to develop competency in and performance basic assembly and/or inspection operations at Integer. The incumbent is expected to follow written procedures to meet production and quality requirements. Adheres to Integer's Values, Behavioral Based Safety process and Integer Associate Quality Policy. Sets up equipment needed for assembly/inspection as per Manufacturing Process Instructions (MPI's) and Quality Work Instructions (QWI's). Understands own tasks and how they relate to others on their team. Works under close Supervision where duties are clearly defined. Will follow Standard Work where applicable. etc. | 9/27/2020 |
| 529 | Integrated DNA Technologies Coralville, IA Lab Technician II (Scientific Manuf.) BS in a science-related field Exp: Not necessary for BS candidates |
Integrated DNA Technologies, Inc. (IDT) is in the business of moving science forward. We are scientists working for scientists. Our innovative tools and solutions for genomics applications are breaking down barriers and inspiring others to dream big and achieve breakthroughs. Every lab has its own responsibilities and plays a crucial part in IDT’s success. Our entry-level scientific lab-based positions are split between three sub-titles, Synthesis, Purification, and Formulation. More detailed descriptions of each can be found below: The Technician II (Synthesis) synthesizes custom oligonucleotides according to the customer’s order. This generally includes synthesis, cleavage, deprotection and QC sampling of the products being made. The Technician II (Purification) purifies custom oligonucleotides according to the customer’s order. This generally includes the sorting, purification, and QC sampling of the products being made. The Technician II (Formulation) formulates custom oligonucleotides according to the customer’s specifications. This generally includes quantification, final packaging, and QC sampling of the products being made. etc. | 9/27/2020 |
| 530 | Intellia Therapeutics Cambridge, MA Process Engineer, AAV Process Development MS in biochemical engineering, molecular biology, or virology Exp: 1-2 year(s) |
Intellia is seeking a skilled and motivated Process Engineer to support AAV process development in the Technical Operations group. The ideal applicant will be experienced and capable in HEK suspension culture and transfection optimization for AAV production. The position requires development, optimization and scale up of AAV production in bioreactors as well as a good understanding of viral production analytics and purification technologies. Experience with documentation and technical transfer to GMP manufacturing is a plus. Responsibilities: AAV upstream process development and transfection optimization. Develop and perform pre-clinical scale up production processes based on QbD. Collaborative integration within Tech Ops and with R&D and Automation groups. etc. | 9/27/2020 |
| 531 | Invenra Madison, WI (Senior) Research Associate - Innovation BS/MS in the biological sciences Exp: 1+ year(s) |
Invenra is seeking an enthusiastic and creative Research Associate or Senior Research Associate with a strong background in molecular biology and protein engineering techniques. This individual will have the freedom to explore new technologies and innovations that can revolutionize Invenra’s current platforms. As part of the Innovation group, the successful applicant will work as part of a team that seeks to improve the efficiency or quality of immune-oncology drug discovery. Details of the job include cutting-edge library construction, recombinant protein expression, developing and optimizing various display strategies, and protein binding experiments. The position requires excellent scientific and problem-solving skills, creative thinking, the ability to try new things, and an enthusiasm for science. etc. | 9/27/2020 |
| 532 | Invenra Madison, WI Research Associate - Cell Biology BS in molecular and cell biology, immunology, or other biological science Exp: 1+ year(s) |
Invenra is seeking a highly motivated Research Associate with a strong background in cellular biology. This individual will support the Invenra antibody discovery platform. Aspects of the job entail mammalian cell culture and assays, analytical flow cytometry, ELISAs, and immunofluorescence/luminescence assays. In addition, the position will involve general ordering and stocking of lab supplies as well as upkeep of standard cell biology equipment (i.e. incubators, biosafety cabinets, etc.). The position requires strong communication and organizational skills as well as attention to detail. etc. | 9/27/2020 |
| 533 | Invitae San Francisco, CA Lab Automation Support Engineer BS/BA in a laboratory discipline Exp: 1+ year(s) |
At Invitae, we have highly automated labs that process samples 7 days a week. To sustain volume growth and maintain high caliber instrument reliability, we are hiring an Automation Support Engineer to join the operations team. The key responsibility of the Automation Support Engineer is to provide support to the clinical lab automation and processes. The work requires excellent attention to detail, effective written and verbal communication skills, the ability to multiple tasks, and prioritize time sensitive tasks. What you will do: Provide prompt troubleshooting support to laboratory operations and escalate situations as needed to subject matter experts in, computing, automation, and laboratory processing. Support laboratory processes by troubleshooting errors related, but not limited to laboratory robotics and LIMS communication. etc. | 9/27/2020 |
| 534 | Invitae San Francisco, CA DNA Extraction Technician BS in clinical laboratory studies or related Exp: 1+ year(s) |
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. etc. | 9/27/2020 |
| 535 | Invitae San Francisco, CA Data Analyst, Lab Operations Background in life sciences Exp: 1+ year(s) |
We are seeking a data analyst to join our team. Responsibilities will include monitoring our product pipeline using custom software tools with the goal of assuring samples move through smoothly. Candidates should have experience with UNIX. They are expected to take initiative to automate tasks and troubleshoot the production process through detail-oriented analysis. An important part of this job is to be able to clearly communicate technical findings to non-technical teammates. etc. | 9/27/2020 |
| 536 | Stryker Saginaw, MI Trauma Sales Associate BS/BA Exp: 1+ year(s) |
What you will do: You will get exposure to the proven winning Stryker Trauma culture that delivers Industry leading results in all market segments. You will receive best-in-class formal Trauma training on product portfolio and selling skills which includes on-the-job training in the operating room. You’ll become an expert on surgical procedures by observing well-over 300 cases in your first year. You will develop well-rounded field exposure to prepare you in all aspects of the selling/ servicing process when a territory opportunity arises. You will develop a high level of competency in Orthopaedic surgical needs and procedures becoming a valuable member of the surgical team and positively impacting surgical outcomes. etc. | 9/27/2020 |
| 537 | Stryker Tucson, AZ Trauma Sales Associate BS/BA Exp: 1+ year(s) |
What you will do: You will get exposure to the proven winning Stryker Trauma culture that delivers Industry leading results in all market segments. You will receive best-in-class formal Trauma training on product portfolio and selling skills which includes on-the-job training in the operating room. You’ll become an expert on surgical procedures by observing well-over 300 cases in your first year. You will develop well-rounded field exposure to prepare you in all aspects of the selling/ servicing process when a territory opportunity arises. You will develop a high level of competency in Orthopaedic surgical needs and procedures becoming a valuable member of the surgical team and positively impacting surgical outcomes. etc. | 9/27/2020 |
| 538 | Stryker San Antonio, TX CMF Associate Sales Representative BS/BA Exp: 1+ year(s) |
At Stryker’s Craniomaxillofacial (CMF) division: You’ll work closely with experienced Sales Representatives and Managers to build your knowledge, skill and comfort with clinical and product knowledge as well as selling styles and techniques. They will serve as your coaches and mentors to share lessons learned for how to build and grow a successful business. You’ll receive training and be expected to study and prepare independently to perform at the highest levels in the operating room, working amongst surgeons and healthcare professionals. The expectations are challenging, yet rewarding. You’ll represent Stryker as a leader in our industry and the marketplace. You’ll have the opportunity to identify and promote solutions and sell products that change our patient’s lives. etc. | 9/27/2020 |
| 539 | Ionis Carlsbad, CA Scientist, Manufacturing BS/MS in chemical engineering Exp: New graduates |
We are seeking a motivated and versatile individual to join our Manufacturing group in an individual contributor, bench Scientist position. The successful candidate will work closely with other scientists in an interdisciplinary team environment to help optimize our solid-phase oligonucleotide manufacturing process, to make improvements to the synthesis of small molecules that make up our supply chain, and to aid in analytical investigations. The candidate should possess a strong work ethic, excellent communication skills, and a demonstrated record of success in a chemical laboratory setting. RESPONSIBILITIES: Optimize manufacturing and purification processes for the solid-phase synthesis of oligonucleotides and oligonucleotide conjugates. Investigate raw material and process-related impurities. etc. | 9/27/2020 |
| 540 | Janssen Research Development San Diego, CA Associate Scientist, Discovery Chemistry MS in synthetic organic or mechanical chemistry Exp: 1+ year(s) |
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. She/he will maintain close interactions with computer assisted design scientists and biologists. Strong people 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. etc. | 9/27/2020 |
| 541 | Just - Evoted Biologics Redmond, WA Associate Scientist, High Throughput Analytical BS in biochemistry, molecular biology, chemical engineering, chemistry or related Exp: 0-5 years |
Just is seeking a motivated and creative Associate Scientist, who desires a significant opportunity to improve worldwide access to biotherapeutics. We are looking for a motivated scientist to join a fast-paced, collaborative, and multidisciplinary team. As a member of the High Throughput Analytical group, you will support process development through application of H/UPLC and CE methodologies. Additional experience with other analytical techniques as well liquid handling robotics is a plus. The ideal candidate has strong written and verbal communications skills and works well independently and in teams. etc. | 9/28/2020 |
| 542 | Just - Evoted Biologics Seattle , WA Associate Scientist, Process Development BS in biochemistry, molecular biology, chemical engineering, chemistry or related Exp: 0-3 years |
Just.Bio is seeking motivated and creative Associate Scientists, who desire a significant opportunity to improve worldwide access to biotherapeutics. We are looking for team members to join a fast-paced, collaborative, and multidisciplinary group to support process development for low-cost biotherapeutic manufacturing. The successful candidates will have some experience in one or more of the following areas including chromatography, filtration, electrophoresis, analytical chemistry, cell culture and/or bioreactor operations. Experience with high throughput, robotic techniques for analytical testing, chromatography, and/or protein expression, as well as statistical design of experiments and/or process modeling, is a plus. The ideal candidate has strong written and verbal communications skills and works well independently and in teams. etc. | 9/28/2020 |
| 543 | Just - Evoted Biologics Redmond, WA Commissioning, Qualification & Validation Engineer I/II – Manufacturing Technical Operations BS in engineering science or related Exp: 1+ year(s) |
Just is seeking a highly motivated Commissioning, Qualification & Validation Engineer that desires a significant opportunity to improve worldwide access to biotherapeutics. The primary focus of this job is to lead the process equipment and utilities commissioning, qualification and validation activities required for late-stage clinical and commercial biologics manufacturing. This comprises all phases of implementation, including ownership of key deliverables such as risk assessments, user requirements specifications, functional and design specifications. The selected candidate will also be responsible for commissioning and qualification protocol generation and execution as well as validation summary reports. Additional job responsibilities will include periodic review and requalification of validated equipment and systems to verify compliance with appropriate regulations and maintaining required change control procedures and impact assessments. etc. | 9/28/2020 |
| 544 | Just - Evoted Biologics Redmond, WA Manufacturing Associate – Cell Culture AS/BS in science or engineering Exp: 1+ year(s) |
Just-Evotec Biologics is seeking a highly motivated Cell Culture Manufacturing Associate that desires a significant opportunity to improve worldwide access to biotherapeutics. This team member will be responsible for the manufacture of mammalian cell-based biotherapeutics for clinical use under cGMP conditions. Manufacturing Associates are initially expected to execute commissioning and validation activities in addition to other start-up support activities. Post start-up activities, the associates are expected to execute process recipes, monitor equipment and processes, perform basic tasks, including sampling, and routine maintenance of lab equipment. The staff member is expected to comply and follow written procedures for safety requirements, cGMP Practices, Standard Operating Procedures and manufacturing documentation. etc. | 9/28/2020 |
| 545 | Just - Evoted Biologics Seattle , WA Process Engineer I – Purification BS in a biological or engineering science Exp: 0-3 years |
Just is seeking a highly motivated entry-level manufacturing Process Engineer that desires a significant opportunity to improve worldwide access to biotherapeutics. This team member will be responsible for the manufacture of mammalian cell-based biotherapeutics for clinical use under cGMP conditions. Under direct/moderate supervision, job responsibilities include set-up, operation, and maintenance of disposable-based manufacturing equipment; execution of manufacturing process operations; and assisting in general lab operations. The staff member is expected to comply and follow written procedures for safety requirements, cGMP Practices, Standard Operating Procedures, and manufacturing documentation. etc. | 9/28/2020 |
| 546 | Just - Evoted Biologics Redmond, WA Process Engineer I/II, Downstream – Manufacturing Technical Operations BS in engineering science or related Exp: 1-3 year(s) |
Just is seeking a highly motivated Process Engineer in the Manufacturing Technical Operations group that desires a significant opportunity to improve worldwide access to biotherapeutics. The primary focus of this job is to support the startup of a first-of-its-kind flexible and reconfigurable cGMP manufacturing facility. The selected candidate will be responsible for supporting the procurement, commissioning, and testing of the process equipment for the new facility, including developing commissioning documentation and standard operating procedures. In addition, the candidate will be responsible for supporting process engineering activities for the new manufacturing plant, including process transfer / tech transfer for clinical and commercial biologics manufacturing, writing technical documentation within cGMP compliant systems, troubleshooting equipment, and introducing new manufacturing technologies such as continuous processing. etc. | 9/28/2020 |
| 547 | Just - Evoted Biologics Redmond, WA Process Engineer I/II, Modeling – Manufacturing Technical Operations BS/MS in chemical or biochemical engineering Exp: 0-2 years |
Just is seeking a highly motivated process engineer in the Manufacturing Technical Operations group that desires a significant opportunity to improve worldwide access to biotherapeutics. The primary focus of this job is to develop mathematical modeling and simulation tools for clinical and commercial biologics manufacturing, data analysis and visualization, empirical and numerical algorithm development, and conveyance of modeling insights through written reports and presentations. The selected candidate will also be responsible for performing bioprocess modeling, writing and revising computer programs, and generating technical reports or documentation. In addition, this team member will gain an understanding of new manufacturing technologies and equipment, including disposable-based systems and continuous processing technologies for a first-of-its-kind flexible and reconfigurable cGMP manufacturing facility. etc. | 9/28/2020 |
| 548 | Karius Redwood City, CA Research Associate BS/MS in biology, molecular biology, genetics, or related Exp: 1-3 year(s) |
As a Research Associate you will work alongside scientific leaders in NGS-based infectious disease diagnostics providing meaningful contributions to making an impact in the lives of patients while contributing to the company’s growth and development . You will be responsible for maintaining process excellence for a state-of-the art NGS infectious disease diagnostic assay by assisting in an established in-house manufacturing process. You will be also involved with several exciting research projects and be at the forefront of non-invasive diagnostics working alongside our scientists to deliver new products. The ideal candidate should have experience with nucleic acids, NGS, or other molecular biology assays to conduct laboratory experiments on research projects under the direction of senior lab personnel. etc. | 9/28/2020 |
| 549 | KBI Biopharma Durham, NC Research Associate BS/MS in chemistry, biochemistry, or related Exp: 0+ year(s) |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. Job Description: Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals. Makes detailed observations and carries out elementary data analysis. Understands experiments and conducts troubleshooting analysis. Maintains and updates knowledge of instrumentation. Notebook upkeep and writing skills. Maintains familiarity with current scientific literature; maintains professional expertise through familiarity with scientific literature. etc. | 9/28/2020 |
| 550 | KBI Biopharma Durham, NC In-Process Support Associate BS in a scientific discipline 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. Job Description: Execute activities according to cGMP regulations and company SOPs. Provide STAT assay coverage including 2nd shift and weekends as required by the manufacturing schedule. Assays include A280 and RP titer. Log samples or verify sample log in outside of standard business hours. etc. | 9/28/2020 |
| 551 | KBI Biopharma Louisville, CO Research Associate - Rapid Analytics Job BS Exp: 0-2 years |
Open position available in 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. Job Requirements: Familiarity with biophysical and protein characterization techniques, such as: SV-AUC, CD, DSC, FTIR, HPLC, UV-Vis. Design and execution of experiments. Routine statistical analysis on generated data sets using JMP or equivalent statistical software. Attention to detail in documentation of experiments in electronic laboratory notebooks. etc. | 9/28/2020 |
| 552 | KBI Biopharma Research Triangle Park, NC Research Associate I/II - Analytical Development BS/MS in chemistry, biochemistry, or related Exp: 0+ year(s) |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. Job Description: Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals. Makes detailed observations and carries out elementary data analysis. Understands experiments and conducts troubleshooting analysis. Maintains and updates knowledge of instrumentation. Notebook upkeep and writing skills. Maintains familiarity with current scientific literature; maintains professional expertise through familiarity with scientific literature. Assures proper labeling, handling, and storage of all chemicals used in the area; assures proper labeling and disposition of hazardous waste in satellite areas; adheres to all safety requirements and follows safe procedures, and attends all required safety and health training, including handling hazardous waste. etc. | 9/28/2020 |
| 553 | KBI Biopharma Durham, NC Manufacturing Associate I/II, Downstream (Nights) BS Exp: 0+ year(s) |
Job Summary: Coordinate and perform cGMP manufacturing operations for manufactured biopharmaceutical products. Ensure the effective use of material, equipment and personnel while making products at high quality levels. Job Description: Assist in execution of procedures for cell culture manufacturing, purification, or support area of manufacturing using SOP's and batch records. Use equipment and techniques related to support, mammalian cell culture and/or harvest and purification. Responsible for completing paperwork for each task, cleaning procedures, aseptic processing techniques, Good Manufacturing Practices (GMP) and laboratory safety practices and procedures. etc. | 9/28/2020 |
| 554 | Fujifilm Diosynth Research Triangle Park, NC Associate Scientist, Cell Culture BS Exp: 1+ year(s) |
The Upstream Process Development group is seeking an Associate Scientist with experience in mammalian or insect cell culture technologies. An Associate Scientist assists in conducting experiments for programs and works with the team to maintain the lab and equipment. The individual monitors on going experiments and can identify unusual occurrences. An Associate Scientist understands and applies knowledge within area of expertise and can take an active role in non-routine process development activities. MAJOR ACTIVITIES AND RESPONSIBILITIES: Conducts routine laboratory experiments using established procedures and protocols. Maintains lab equipment, supplies and work area. Quality of work is complete and technically sound to ensure integrity of research. etc. | 9/21/2020 |
| 555 | Fujifilm Diosynth Research Triangle Park, NC Process Scientist/Engineer I BS Exp: Not necessary for BS candidates |
The Process Scientist/Engineer I represents the technical operations department before FDBU customers, regulatory agencies and management. This individual will manage the new client process and ensure project objectives are completed. The Process Scientist/Engineer will also contribute to the technology transfer of multiple projects at various project life-cycle stages (clinical material to commercial supply). Additionally, this individual must possess strong process understanding to implement and execute process risk review and process/cleaning qualification and validation activities. etc. | 9/21/2020 |
| 556 | Fujifilm Diosynth Research Triangle Park, NC Process Scientist/Engineer II MS Exp: Not necessary for MS candidates |
Responsibilities: May support technical transfer of client project in and to manufacturing as applicable. Summarizes and report data. Interacts with supervisor and reports results and interpretation of experiments, project deliverables, and process readiness. Supports capital projects by providing technical expertise. Supports new project site-fit assessments as needed. Assists in developing SOPs and engineering documents. Familiar with relevant literature. etc. | 9/21/2020 |
| 557 | Fujifilm Diosynth Research Triangle Park, NC Scientist I, Analytical Methods Transfer MS Exp: 1+ year(s) |
The successful candidate requires the following knowledge, skills and abilities: One to three years of applicable hands on experience in Plate Based methods. Additional experience in one or more of the following fields: HPLC/UPLC, capillary electrophoresis, spectroscopy or biophysical characterization methods. Good interpersonal skills, the ability to work individually or as part of a team, and problem solving capabilities of standard laboratory techniques. Have strong oral communication skills. In addition, the successful candidate must be comfortable multi-tasking in a fast-paced environment with defined deliverables and deadlines. GMP experience a plus. etc. | 9/21/2020 |
| 558 | Fujifilm Diosynth Research Triangle Park, NC Downstream Production Technician HS diploma/BS/BA Exp: 1+ year(s) |
Fujifilm Diosynth Biotechnologies, U.S.A., Inc. is seeking Downstream Production Technicians (all levels) to work in our Downstream Manufacturing group. The successful candidate will execute Development and Production processes as well as the accompanying documentation. This position could either be a day shift position (7:00 am – 7:00 pm) or a night shift position (7:00 pm – 7:00 am). The candidate hired will be working on day shift for the first six months for training, and then transition to the night shift. Main areas of responsibilities include: Executing development and production processes as well as process documentation. Understanding processing principles and scientific theory behind operations steps. etc. | 9/21/2020 |
| 559 | Fujifilm Diosynth College Station, TX Assistant Scientist- AD BS in chemistry, biology, or related life science Exp: Not necessary for BS candidates |
Essential Functions: Assist in the transfer, development, and optimization of customer programs. Independent operation of instrumentation in the PD laboratories. Assist in conducting, data plotting and reporting the results of laboratory experiments. Monitor ongoing experiments for any unusual occurrences. Maintenance of lab equipment, supplies and records. Execution of basic experimental protocols. Maintaining detailed laboratory notebooks following FDBT procedures. Perform all other duties as assigned. etc. | 9/21/2020 |
| 560 | Fujifilm Diosynth College Station, TX Associate Scientist – Analytical Method Transfer BS/MS in chemistry, biology, or related life science Exp: 1 year |
Essential Functions: Execute method transfers/qualifications/validations based on regulatory guidelines and industry best practices. Perform assays to evaluate the accuracy, precision, specificity, linearity, robustness, and detection/quantitation limits of analytical methods. Maintain laboratory instrumentation and assist with vendor qualifications. Develop expertise on a subset of analytical methods and participate in method troubleshooting activities. Maintain awareness of project timelines and milestones and openly communicate scheduling challenges. Assist in the preparation of technical documents including protocols and reports. Finalize analytical test methods; route documents for approval within Master Control. Interface with other groups to drive project success, including Analytical Development, Project Management, Quality Control, and Quality Assurance. etc. | 9/21/2020 |
| 561 | GeneDX Gaithersburg, MD Primary Analyst I (FT, 40 Hours) MS in medical technology or related life science Exp: Not necessary for MS candidates |
Responsibilities include: Case Analysis -- Efficiently analyzes all data (ABI, NG, Exome, Exon Array, MLPA, qPCR, Genome Array, etc.) and completes all primary analysis related steps according to standard procedures. Performs at a consistent level of analysis by completing a reasonable number of analysis steps with minimal errors. Reliably identifies variants meeting confirmation criteria and sends them for confirmation using appropriate methods, as applicable. Aims to identify novel situations and seek prompt and appropriate advice on how to proceed. Makes sure all relevant aspects of a case are complete and either sends them to review or logs them out, as appropriate. etc. | 9/21/2020 |
| 562 | GeneDX Gaithersburg, MD Lab Technician, Microarray (FT, 40 Hours) BS in medical technology or related Exp: 0-1 year(s) |
Responsibilities include: Learns and follows the established standard operating procedures for specimen handling and processing, test analysis, reporting of results to team leads, supervisors and test managers, and record-keeping. Adheres to quality control policies; documents all quality control activities, instrument and procedural calibrations, reagent preparation and testing, and instrument maintenance performed. Identifies problems that may adversely affect test performance, take authorized corrective action, and notifies key individuals. Detects when test performance is not within acceptable levels, and documents all corrective action. etc. | 9/21/2020 |
| 563 | GeneDX Gaithersburg, MD DNA Extraction Technician (FT, 40 Hours) BS in medical technology or related Exp: 0-1 year(s) |
Responsibilities include: Learns and follows the established standard operating procedures for specimen handling and processing, test analysis, reporting of results to team leads, supervisors and test managers, and record-keeping. Adheres to quality control policies; documents all quality control activities, instrument and procedural calibrations, reagent preparation and testing, and instrument maintenance performed. Identifies problems that may adversely affect test performance, take authorized corrective action, and notifies key individuals. Detects when test performance is not within acceptable levels, and documents all corrective action. etc. | 9/21/2020 |
| 564 | GeneDX Gaithersburg, MD DNA Sequencing Lab Technician I BS in medical technology or related Exp: 0-1 year(s) |
Responsibilities include: Learns and follows the established standard operating procedures for specimen handling and processing, test analysis, reporting of results to team leads, supervisors and test managers, and record-keeping. Adheres to quality control policies; documents all quality control activities, instrument and procedural calibrations, reagent preparation and testing, and instrument maintenance performed. Identifies problems that may adversely affect test performance, take authorized corrective action, and notifies key individuals. Detects when test performance is not within acceptable levels, and documents all corrective action. etc. | 9/21/2020 |
| 565 | GeneDX Gaithersburg, MD NGS Lab Tech BS in medical technology or related Exp: 0-1 year(s) |
Responsibilities include: Learns and follows the established standard operating procedures for specimen handling and processing, test analysis, reporting of results to team leads, supervisors and test managers, and record-keeping. Adheres to quality control policies; documents all quality control activities, instrument and procedural calibrations, reagent preparation and testing, and instrument maintenance performed. Identifies problems that may adversely affect test performance, take authorized corrective action, and notifies key individuals. Detects when test performance is not within acceptable levels, and documents all corrective action. etc. | 9/21/2020 |
| 566 | GeneDX Gaithersburg, MD Lab Technician, Microarray BS in medical technology or related Exp: 1 year |
Responsibilities include: Implements the standard operating procedures for specimen handling and processing, test analysis, reporting of results to team leads, supervisors and test managers, and record-keeping. Adheres to quality control policies; documents all quality control activities, instrument and procedural calibrations, reagent preparation and testing, and instrument maintenance performed. Identifies problems that may adversely affect test performance, takes authorized corrective action, and notifies key individuals. Detects when test performance is not within acceptable levels, and documents all corrective action. etc. | 9/21/2020 |
| 567 | Gilead Oceanside, CA Sr. Research Associate I, Process Development (Protein Purification) MS Exp: 0+ years |
Gilead Sciences is seeking a Sr. Research Associate I with experience in protein purification process development to support operations at our biologic’s development and manufacturing site in Oceanside California. Specific Responsibilities and skills for Position: The successful candidate will have a working understanding of downstream process development including centrifugation, normal and tangential flow filtration, chromatography operations, and virus clearance. The ability to demonstrate hands on experience in several of these areas is expected. Experience with multiple modalities (monoclonal antibodies, antibody drug conjugates, virus particles) produced in microbial and mammalian expression systems is a plus. The candidate is expected to work effectively within the purification team to help design and execute experiments supporting process definition, optimization, and characterization with an increasing level of independence. etc. | 9/21/2020 |
| 568 | Gilead Oceanside, CA Research Associate, Biologics Analytical Operations (Analytical Development) BA/BS in chemistry, biochemistry, or related Exp: 0-2 year(s) |
Job Responsibilities: Under general supervision, performs analytical testing for biologics GMP and process development activities. Follows and incorporates GMP, GDP, and GLP during daily activities within an analytical biochemistry lab setting. Plans and organizes details of experiments for protein analysis. Operates scientific equipment and instruments. Experience and understanding of wet chemistry techniques, chromatography and/or capillary electrophoresis preferred. Uses data, reports, and previous results to identify inappropriate variances and concerns. Participates in group meetings. Presents data or prepares information for others to present. Works with immediate supervisor and teammates on problems of moderate complexity. etc. | 9/21/2020 |
| 569 | Ginkgo Bioworks Boston, MA QA/QC Engineer BS in chemistry, chemical engineering, or related Exp: 1-6 year(s) |
To realize our dream of building a next-generation organism company, we must ensure that quality is maintained during all stages of our projects, through to the successful deployment of our organisms and processes. Therefore, we’re seeking a QA/QC Engineer with chemical laboratory experience to help define product specification and maintain a Quality Management System. Plus, you’ll ensure that Ginkgo, our customers, and our contract manufacturers have the necessary methods and processes in place, so that we maintain compliance across any required regulatory standard and consistently meet the defined product and process specifications. Responsibilities: Develop, validate, and execute analytical methods, focusing primarily on accurate and precise quantitation. Perform QA/QC data collection, data integration, and data archiving, with the use of Ginkgo’s proprietary LIMS (laboratory information management system). etc. | 9/21/2020 |
| 570 | Ginkgo Bioworks Boston, MA Downstream Process Engineer BS in chemical engineering, biotechnology, or related Exp: 1-6 year(s) |
To realize our dream of building a next-generation organism company, each of our organisms needs to be successfully deployed. Ensuring that the deployed product reproducibly meets customer and market specification in an economically viable process is critical to Ginkgo’s success. Therefore, we’re seeking a Downstream Process Engineer to help tackle this ambitious challenge. With your passion for process development, and a particular interest in downstream product recovery and purification, you’ll be responsible for designing, developing, and deploying product recovery and purification processes for a variety of products across several scales and sites. Responsibilities: Design and execute laboratory and pilot scale experiments, leading to the definition of commercially viable processes that leverage Ginkgo's engineered organisms. Perform bench scale assays and proof-of-concept experiments. etc. | 9/21/2020 |
| 571 | Ginkgo Bioworks Boston, MA Medical Technologist (Night Shift) BS/MS in a chemical, physical, or biological science Exp: 1+ year(s) |
We’re seeking highly motivated Medical Technologists to perform routine testing in our high-complexity CLIA laboratory. With a strong focus on quality, accuracy, and efficiency, you’ll be responsible for accessioning received samples, and completing quality control, calibration, maintenance, and proficiency testing in accordance with current laboratory procedures. As a member of Ginkgo’s Clinical Laboratory Operations Team, our Medical Technologists will have a key role in ensuring the success of this important initiative. Please note: this is a fixed-term contractor role for the night shift in our rotation. Anticipated hours are 8:00pm - 8:00am on a "4 days on / 4 days off" shift schedule (which will require some weekend hours). etc. | 9/21/2020 |
| 572 | Ginkgo Bioworks Boston, MA Medical Technologist (Day Shift) BS/MS in a chemical, physical, or biological science Exp: 1+ year(s) |
We’re seeking highly motivated Medical Technologists to perform routine testing in our high-complexity CLIA laboratory. With a strong focus on quality, accuracy, and efficiency, you’ll be responsible for accessioning received samples, and completing quality control, calibration, maintenance, and proficiency testing in accordance with current laboratory procedures. As a member of Ginkgo’s Clinical Laboratory Operations Team, our Medical Technologists will have a key role in ensuring the success of this important initiative. Please note: this is a fixed-term contractor role for the day shift in our rotation. Anticipated hours are 8:00am - 8:00pm on a "4 days on / 4 days off" shift schedule (which will require some weekend hours). etc. | 9/21/2020 |
| 573 | Global Pharma Tek Edison, NJ Clinical Project Assistant BS/BA in pharmacy, pharmaceutical science, healthcare informatics or related Exp: 1-2 year(s) |
Job Duties: Responsible for strategic and operational activities of clinical research studies in blood cancer metabolism to ensure adherence to intended timelines and achievements of study goals, while ensuring quality by FDA, EMEA, ICH and GCP guidelines. Facilitating interdisciplinary activities, participating in the clinical trial working group (CTWG), Site Management Team (SMT), and internal team meetings to meet the goals and established timelines. Providing oversight in clinical research Organization (CRO), Central labs and other external vendors to ensure deliverables are met and methods of communication are developed to facilitate an efficient workflow. Providing oversight of activities related to safety reporting compliance. Provide study tracking support (CTMS tracking, start-up tracking, milestone tracking, close-out tracking) and study updates, as requested. Provide coordination and tracking of clinical supply shipments, equipment, and study-specific laboratory samples. etc. | 9/21/2020 |
| 574 | Global Pharma Tek Edison, NJ Sr. Validation Engineer BS in biochemistry, chemistry, pharmaceutical sciences, or related Exp: 1-2 year(s) |
Job Duties: Writing of Validation documents per Food and Drug Administration (FDA)/Company Guidelines. Utilizing the information from User Manuals, Equipment Operation/Use/Maintenance etc. information and drafting of specification documents and validation protocols for GMP Liquid Dose Manufacturing (LDM) clinical Drug Product (DP) that impact manufacturing facility (processes, equipment (like autoclave, lyophilizers, depyrogenation tunnels). Creation/modification of change control requests, project validation plans and maintaining project within timelines. If any changes were deemed necessary in the equipment (Changes may be like changes in parts or operation of the equipment or changes in procedure or changes in Training of personnel or On-boarding/retiring equipment etc.) I will create a change request in global Quality Tracking System (gQTS), a Trackwise application and thereby monitoring these changes by performing required assignments throughout the project to completion (closing change request) for the current filling and sterilization equipment and install/qualify the new equipment. etc. | 9/21/2020 |
| 575 | Global Pharma Tek Edison, NJ Submission Specialist – Regulatory Affairs BS/BA in regulatory affairs, healthcare administration, or related Exp: 1-2 year(s) |
Job Duties: Providing direct support to submission project teams, internal RA stakeholders and all functional disciplines responsible for developing and delivering components for submissions. Performing hands-on daily submission compilation and publishing activities associated with preparation of various dossier types and safety reports, for both new product marketing applications and/or marketed product maintenance packages. Performing overall quality of the assigned documents and dossiers which must comply with all internal Bayer best practices, meet global regulatory requirements, and facilitate the review and timely approval by appropriate regulatory authorities. Reviewing the eCTD compliance of dossier-relevant R&D documents/reports from technical perspective. Supporting the compilation of global dossiers and to deliver technically compliant submission documents/reports, which contribute to the development of submissions that meet the technical requirements and standards set by relevant health authorities. etc. | 9/21/2020 |
| 576 | Global Pharma Tek Edison, NJ Regulatory Affairs Compliance Specialist BS/BA in pharmaceutical science, regulatory affairs, or related Exp: 1-2 year(s) |
Job Duties: The Regulatory Affairs (RA) Compliance Specialist will be responsible for RA Labeling compliance associated with labeling artwork development and revisions for products which may include Rx, OTC/Nutritionals, Cosmetics, and Devices. Specialist will verify the changes in accordance to regulatory requirements to identify impact to product labels. As a key team member, contributes to the labeling processes and procedures to enhance existing practices. Provide Regulatory compliance support in the development, revision, review, and approval of labeling content for regulatory submission, as well as any post marketing labeling changes. Review new and revised labeling for accuracy and for appropriate regulatory requirements. etc. | 9/21/2020 |
| 577 | Global Pharma Tek Edison, NJ Equipment Validation Engineer BS in mechanical or industrial engineering or related Exp: 1-2 year(s) |
Job Duties: Provide technical support in developing, authoring, and executing the Commissioning, Installation and Qualification protocols for the chromatography skids and other supporting equipment that are used in the production of drug. Develop, Implement and Install filter integrity testing methods to available automated Filter Integrity Testers (FITs) available on site to verify the integral of the vent filters that will used in the process for WFI Tanks, Autoclaves, supply clean compressed air and as required. Prepare protocols and reports for Validation Project Plan, Validation Master Plan, IQ, OQ, OQ, Traceability Matrix, Engineering test Plans, and Commissioning test strategies following the site Good Data and Documentation Practices (GDP) during protocol execution for qualifying the system or facility. etc. | 9/21/2020 |
| 578 | Global Pharma Tek Edison, NJ Laboratory Equipment/Instrument Qualification Engineer BS in pharmacy, chemistry, or related Exp: 1-2 year(s) |
Job duties: Execute Validation and Qualification protocols which include installing, operating and maintaining of GMP Lab Equipment and Instruments (HPLC, UV-Vis Spectrometers, FTIR, GC, pH meters, Conductivity meters, Analyzers etc.) and manufacturing equipment like sterilizers and autoclaves to confirm if the instrument is compatible and compliant with Manufacturing, analysis, Company and FDA regulations. Author, review and approve validation and qualification documents for Lab Equipment/Instruments and manufacturing equipment in compliance with Pharma and FDA guidelines through Document Management system tool. Perform validation and qualification documents include User requirement specifications, functional requirement specifications, Installation Qualifications (IQ), Operational Qualifications (OQ), Performance Qualifications (PQ), Validation summary reports, Change Control etc. for various lab instruments utilized by Quality control and Quality assurance teams. etc. | 9/21/2020 |
| 579 | Global Pharma Tek Edison, NJ Associate Operations Specialist BS in pharmacy, pharmacology, or related Exp: 1-2 year(s) |
Job duties: Review, assess and process Lifecycle Safety data and information, across all service lines received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members. Receive, triage, review and process data from various sources on time, within budget and meet quality standards. Perform data entry for tracking and safety database, coding relevant medical terminology, writing, descript narratives, generating queries pertinent to the case, performing quality control, assisting with reconciliation, driving case closure, coordinating translations and ensuring reports are sent to the customer within assigned deadlines. etc. | 9/21/2020 |
| 580 | GRAIL Menlo Park, CA Laboratory Technician I/II BS in a relevant scientific field Exp: 1-5 year(s) |
GRAIL is seeking a Laboratory Technician I/II for the R&D Laboratory Management team, who will be primarily responsible for ensuring the efficient operation of GRAIL Research and Development activities. The ideal candidate is a detail-oriented, dynamic team player with experience in both automated and manual molecular biology workflows combined with strong interest in NGS methodologies. The candidate will be expected to partner with many functions of our organization - Automation, Product Development, LIMS, Supply Chain, Biosample Operations, and Clinical Lab - to ensure the successful completion of R&D projects and general Operational support. etc. | 9/21/2020 |
| 581 | GRAIL Menlo Park, CA Equipment Engineering Technician BS in an engineering or scientific discipline Exp: 0-2 years |
As an Equipment Engineering Technician, you are responsible for supporting laboratory equipment management procedures, in alignment to our internal Quality Management System, to ensure superior performance within Laboratory Operations. This will include global laboratory equipment support, sustainment, and operations activities across Production/Clinical, Product Development, Research and Development laboratories, in accordance with CLIA, cGMP and/or GLP guidelines. You Will: Support global laboratory equipment documentation by maintaining internal equipment records into our database/repository. Assist with internal laboratory equipment inventory processes and procedures. etc. | 9/21/2020 |
| 582 | Grand River Aseptic Manufacturing Grand Rapids, MI Validation Engineer I BS in engineering or related Exp: 0-3 years |
Support validation of cGMP equipment, facilities and processes. These duties will include, but are not limited to: and validation of laboratory systems, production equipment, manufacturing processes and utilities. ESSENTIAL DUTIES & RESPONSIBILITIES: Assist with maintaining and revising validation procedures. Establish and maintain good practices with regards to processes and/or internal conditions leading to an aseptic environment. Establish and execute programs covering equipment, processes, cleaning, process and computer system validation. Assure that all validation is performed to conform to GRAM’s and cGMP requirements. Provide validation support to internal customers such as Technical Services, Quality Control, Manufacturing and other users of validation services. etc. | 9/21/2020 |
| 583 | Gritstone Oncology Cambridge, MA Research Associate - GMP NGS BS Exp: 1+ year(s) |
The primary role of the Research Associate is to be responsible for the execution of 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. etc. | 9/21/2020 |
| 584 | Harpoon Therapeutics South San Francisco, CA Research Associate, Protein Purification BS/MS in biochemistry, biotechnology, molecular biology, or related Exp: 1-5 year(s) |
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 our functional group, this individual will work closely with other team members within Protein Science and partner with other functional areas including Biology, New Technologies, and Translational Medicine. The ideal candidate will have strong technical aptitude for lab work and a problem-solving mindset that is diligent and flexible. Our Research organization is comprised of a small but diverse group of scientists with a wide range of experience and backgrounds. etc. | 9/21/2020 |
| 585 | Harpoon Therapeutics South San Francisco, CA Research Associate, Biology BS/MS in cell biology, biochemistry, or related Exp: 1+ year(s) |
The Research Biology group at Harpoon Therapeutics seeks a Research Associate to join our team. Responsibilities include testing of samples in support of both preclinical development and clinical programs, assay development and optimization, and collection of data in support of regulatory filings. Applicants should be capable of working flexibly and expeditiously in a collaborative, innovative and inspiring environment. The ideal candidate will have experience with mammalian cell culture, stable cell line generation, luciferase assays, flow cytometry, and bioassay automation. Good communication skills, good planning, and an ability to meet deadlines are essential. etc. | 9/21/2020 |
| 586 | Helix San Diego, CA Research Assistant, Research & Development BS/MS in a biological science or related Exp: 1 year |
We are searching for a highly motivated and team-oriented Research Assistant (RA) to support a wide variety of molecular biology, biochemical, and extraction techniques to support projects focused on viral infection. As an RA at Helix, you will work in a dynamic and fast-paced environment to perform robust, scalable COVID-19 testing, where you will perform testing with the overall goal of providing results that will be used for the assay development, diagnosis and management of COVID-19. As a Research Assistant, Research & Development you will: Assist in running molecular assays and processes for Next Generation Sequencing (NGS) for use in a high throughput clinical laboratory. Perform routine tasks for the group. Execute experiments related to NGS assay. etc. | 9/21/2020 |
| 587 | Helmer Scientific Noblesville, IN Assembler Level II HS diploma or equivalent Exp: 1-3 year(s) |
The Assembler II performs repetitive assembly tasks using basic hand tools to build temperature controlled storage units, refrigerators/freezers and thawing systems or under counter temperature controlled storage units. Cross-trained to perform specialty functions in the following areas: brazing, final testing, charging or wiring. Promotes Helmer values as demonstrated in personal productivity and quality of work, management of internal/external relationships, actively seeking out and participating in Continuous Improvement practices, and willingness to engage and support team initiatives. Comply with workplace safety procedures. Regular and reliable attendance, which includes punctuality and working scheduled overtime, is necessary to meet our commitment to provide quality products and service to our customer. etc. | 9/21/2020 |
| 588 | Helmer Scientific Noblesville, IN General Fabricator 2nd Shift HS diploma or equivalent Exp: 1-3 year(s) |
The General Fabricator: Operates painting and other operations in the fabrication department. Promotes Helmer values as demonstrated in personal productivity and quality of work, management of internal/external relationships, actively seeking out and participating in Continuous Improvement practices, and willingness to engage and support team initiatives. Comply with workplace safety procedures. Regular and reliable attendance, which includes punctuality and working scheduled overtime, is necessary to meet our commitment to provide quality products and service to our customer. etc. | 9/21/2020 |
| 589 | Helmer Scientific Noblesville, IN Fabrication Technician HS diploma or equivalent Exp: 1-3 year(s) |
The Fabrication Technician: Operates and maintains the laser, Turret Punch, CNC press brakes or panel bender. Will be cross-trained to perform responsibilities on any of these machines. etc. | 9/21/2020 |
| 590 | Helmer Scientific Noblesville, IN Assembler Level I 2nd Shift HS diploma or equivalent Exp: 1-3 year(s) |
The Assembler I: Performs repetitive assembly tasks using basic hand tools to build temperature controlled storage units, refrigerators/freezers and thawing systems or under counter temperature controlled storage units. May clean and pack units. Promotes Helmer values as demonstrated in personal productivity and quality of work, management of internal/external relationships, actively seeking out and participating in Continuous Improvement practices, and willingness to engage and support team initiatives. Comply with workplace safety procedures. Regular and reliable attendance, which includes punctuality and working scheduled overtime, is necessary to meet our commitment to provide quality products and service to our customer. etc. | 9/21/2020 |
| 591 | Helmer Scientific Noblesville, IN Assembler I - Clean & Pack HS diploma or equivalent Exp: 1-3 year(s) |
The Assembler I - Clean & Pack: Performs repetitive assembly tasks using basic hand tools to build temperature controlled storage units, refrigerators/freezers and thawing systems or under counter temperature controlled storage units. May clean and pack units. etc. | 9/21/2020 |
| 592 | Helmer Scientific Noblesville, IN Assembler Level I HS diploma or equivalent Exp: 1-3 year(s) |
The Assembler I: Performs repetitive assembly tasks using basic hand tools to build temperature controlled storage units, refrigerators/freezers and thawing systems or under counter temperature controlled storage units. May clean and pack units. Promotes Helmer values as demonstrated in personal productivity and quality of work, management of internal/external relationships, actively seeking out and participating in Continuous Improvement practices, and willingness to engage and support team initiatives. Comply with workplace safety procedures. Regular and reliable attendance, which includes punctuality and working scheduled overtime, is necessary to meet our commitment to provide quality products and service to our customer. etc. | 9/21/2020 |
| 593 | Helmer Scientific Noblesville, IN Sustaining Mechanical Product Support Engineer 1 BS in mechanical or related engineering Exp: 0-3 years |
The Sustaining Mechanical Product Support Engineer 1: Provides product support to Manufacturing and Sustaining Engineering departments through the development, documentation and production support for Helmer product portfolio. Support projects, specification updates and engineering requirements based on product and stakeholder requirements. Enhance part and product design, quality, manufacturability, and serviceability through sustainment and continued improvement of mechanical designs including assembly/component design and testing, tolerance stack, non-conforming product evaluation and value engineering. etc. | 9/21/2020 |
| 594 | Exelixis Alameda, CA Temporary Purchasing Assistant AA/BA Exp: Not necessary for AA/BA candidates |
Responsible for supporting the daily tasks, functions, and responsibilities of the Procurement Department and the Indirect Buyers which will focus on, but is not limited to, entering Vendor Master data into SAP for new vendors and vendor changes including following security procedures to confirm and document change requests, placing routine orders as assigned, and, follow-up on orders. Additional projects as assigned by manager. Position Requirements: ESSENTIAL DUTIES AND RESPONSIBILITIES: Responsible for supporting the day-to-day purchasing for the company by: Managing vendor data entry and vendor changes in the ERP system. Expediting and PO follow-up. Filing and clerical support duties. etc. | 9/14/2020 |
| 595 | Exelixis Alameda, CA Assistant Research Scientist I (Pharmacokinetics/Pharmacodynamics) BA/BS Exp: 0-2 years |
The successful and highly motivated candidate will support the in vivo pharmacology research program and contribute to the multidisciplinary research team by designing and executing in vivo studies to determine pharmacokinetics and pharmacodynamics relationships and efficacy of optimized leads. Position Requirements: ESSENTIAL DUTIES AND RESPONSIBILITIES: Conduct in vivo studies in mouse and/or rat models to assess pharmacological characteristics of preclinical drug candidates. Daily dosing (po, iv, ip) of preclinical drug candidates to mice or rats, followed by blood and tissue collection for pharmacokinetic or pharmacodynamic analyses. Tumor implantation and measurement for long-term efficacy and pharmacodynamic studies. Use of aseptic techniques to grow and scale up tumor cells for implantation in mouse models. etc. | 9/14/2020 |
| 596 | Exonbio San Diego, CA Research Associate MS in biology Exp: 1 year |
We are looking for a RESEARCH ASSOCIATE to join our antibody development team. Requirements: One year experience in Cell culture and banking, PCR, Protein purification with AKTA. | 9/14/2020 |
| 597 | Bio-Techne San Marcos, CA Packaging Technician HS diploma or equivalent Exp: 1-2 year(s) |
As a packaging technician you will perform filling, kitting, and labeling functions. Key Responsibilities: Assist in the setup and running of automated liquid filling, labeling and packaging equipment. Assist in the setup and running of manual liquid and powder portable filling equipment. Perform daily filling, labeling, kitting duties according to the production schedule. Comply with Good Manufacturing Practices (GMP’s) and Quality Systems Regulations (QSR). General organization of filling, labeling and packaging tasks. Inspect all materials being issued to and returning from shop orders. Accurately count and return all materials. Maintain supplies for the CER, and packaging areas. etc. | 9/14/2020 |
| 598 | Bio-Techne Minneapolis, MN Research Associate BS/BA Exp: 0-3 years |
This position is responsible for filtering, aliquoting, and storing finished proteins products using aseptic techniques in a GMP Lab, following GMP guidelines. Run lyophilizer and perform fill finish (vialing, stoppering, crimping, and labeling of products). Documents batch records following GMP guidelines. Manufacture and bag ProDots. Buffer manufacture for fill finish. (80%) Documentation: SOPs, and for validation/maintenance/cleaning of equipment and facilities. (20%) Key Responsibilities: Filter, aliquot, and bottling of product using aseptic techniques. Run lyophilizer and perform fill finish (vialing, stoppering, crimping, and labeling of products). Manufacture and bag ProDots. etc. | 9/14/2020 |
| 599 | Bio-Techne Devens, MA Advanced Quality Technician BS Exp: 1+ year(s) |
Advanced Quality Technician reports to the Quality Control Manager and is responsible for in-process and final QC testing of Bionostics products. In addition, Advanced Quality Technician participates in instrument validations, performs lab maintenance activities, initiates collaborations, monitors laboratory and process inventories, conducts device history record review, and creates certificates of analysis for commercial products. Key Responsibilities: Understands and adheres to all quality technician job requirements. Follows work instructions carefully and demonstrates good documentation practices. Documents results, processes testing, and refers to past batch records when needed. etc. | 9/14/2020 |
| 600 | Bio-Techne Wallingford, CT QC Technician AS/AA Exp: 0-3 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 (see https://www.proteinsimple.com/ella.html). Key Responsibilities: Understand and follow appropriate quality protocols: Quality Manual; Record Keeping Guidelines; General understanding of Quality body of knowledge (Inspection plans, sampling, etc.); Safety procedures; Department specific SOP’s. etc. | 9/14/2020 |
| 601 | Bio-Techne San Jose, CA Manufacturing Technician (Kitting) Unspecified Exp: 0-1 year |
The technician will work as part of the kitting team under the planning group to complete all tasks related to subassemblies and top-level product kits, packaging and labeling to prepare products for warehousing and/or shipments to customers. Key Responsibilities: Follow SOPs, work instructions and/or drawings to ensure product specifications are met. Assemble, label, and package a wide variety of kits: product components, sub kits and top-level kits. Prepare a collection of product components, sub kits and top-level kits for shipping (Pick to Order, PTO). Prepare demo kits as needed. Stage material for kitting operation. Inspect collection of kit components for expiration dates. Submit daily kitting numbers and associated types (sub kits / top-level kits) to manager at end of shift. etc. | 9/14/2020 |
| 602 | Bio-Techne Minneapolis, MN Advanced Research Associate MS in biology, cell biology, immunology, or related scientific discipline Exp: 0-2 years |
The responsibilities of this position are to develop bioassays on proteins and antibodies to ensure quality products. Maintain cell lines and isolate primary cells for use in the assays. Key Responsibilities: Develop cell-based and functional ELISA binding bioassays for new protein products and improve existing bioassays. Review literature and discuss the new products and experiments with the supervisor. Implement new bioassays under the direction of the supervisor. Write SOPs for new developed bioassays and perform stability testing on new products. Perform product bioassays following the SOPs and assist at all stages of protein expression and purification. Maintain cell lines and isolate primary cells from human or animal blood or tissues for use in bioassays. Freeze stock of cells for future use. etc. | 9/14/2020 |
| 603 | Bio-Techne San Marcos, CA Chemist I - R&D (Temporary) BS/BA Exp: 0-3 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. Key Responsibilities: Assist with preparation and/or development of new products using approved procedures and keep detailed and accurate records. Set up and conduct experiments that help further new product development. Follow standard operating procedures. Perform in process analysis and determine adjustments to bring analytes into specification. etc. | 9/14/2020 |
| 604 | Exsurco Wakeman, OH Assembly Technician HS diploma Exp: 3 months |
Primary role is to perform all forms assembly activities including equipment setup and tear down where required as well as in-process verifications. In addition, this position includes several cross-functional responsibilities comprising Shipping, Receiving, Job Picking, Warehousing and Plant Cleaning and some Maintenance activities. This position also has responsibilities associated with Servicing returned products (disassembly and reassembly, diagnosis and report writing). RESPONSIBILITIES: The duties & responsibilities of the Assembly Technician include, but are not necessarily limited to the following: Perform bench-type processes to complete mechanical and electrical assemblies and sub-assemblies, using hand tools, and electronic and pneumatic tooling. Assemble Exsurco product and equipment as required. etc. | 9/14/2020 |
| 605 | Fate Therapeutics San Diego, CA Research Associate III / II, Genomics Unspecified Exp: 1-3 year(s) |
Fate Therapeutics is currently seeking a talented and highly motivated Research Associate with a background in nucleic acid purification and next generation sequencing (NGS) library processing to join a multidisciplinary team dedicated to the discovery and characterization of novel induced pluripotent stem cell (iPSC)-derived cellular therapeutics. The candidate will play a key role in Fate’s Genomics group, executing-based assays in support of Fate’s efforts to generate and characterize best-in-class iPSC-derived cellular therapies. The ideal candidate will be highly collaborative and communicative and have extensive hands-on experience in extracting and purifying DNA and RNA from cells and tissues for use in NGS. This position will require adherence to tight deadlines, strong independent and collaborative research abilities, a high level of organization, and the ability to communicate effectively across multidisciplinary teams. etc. | 9/14/2020 |
| 606 | Fate Therapeutics San Diego, CA Clinical Manufacturing Associate BS/BA in a biological science Exp: 1-2 year(s) |
Fate is currently seeking a motivated associate to join our Clinical Manufacturing team. The successful candidate will execute CMC studies and produce cell stocks in support of Fate's clinical development programs. The position will be responsible for ordering and maintaining lab equipment and supplies, performing experiments to qualify process improvements for manufacture of Fate's products in clinical development, and performing analysis of data. The position will provide technical support for Fate manufacturing and process development activities. The successful candidate will have excellent organizational and communication skills, a keen attention to detail and thrive in a team environment. etc. | 9/14/2020 |
| 607 | FHC Bowdoin, ME Shipping & Receiving Technician AS/BS Exp: Not necessary for AS/BS candidates |
The Shipping & Receiving Technician is responsible for all of FHC, Inc.’s incoming and outgoing shipments. The position requires a basic knowledge of FHC products and an extensive knowledge of shipping requirements. Interfacing with multiple departments to ensure the best delivery dates and methods are used to meet customers’ requirements and to assure a unique and satisfying experience for both internal and external customers. ESSENTIAL DUTIES AND RESPONSIBILITIES: Other duties may be assigned. Responsible for processing Return Material Authorizations RMAs Inbound and Outbound. etc. | 9/14/2020 |
| 608 | Finch Somerville, MA Process Development Associate BS in chemical or biomedical engineering, chemistry, or biochemistry Exp: 0-2 years |
Duties / Responsibilities: Assist in planning, executing, and documenting studies related to design of novel drug products. Support scale-up and technical transfer of production processes to GMP Manufacturing. Assist with troubleshooting, root cause analysis, and identification of corrective actions to support Pharmaceutical Development or GMP Manufacturing equipment and process issues. Work cross-functionally across Quality, Research, Clinical, and Manufacturing teams to achieve company goals. Source and maintain relationships with vendors and Contract Manufacturing Organizations. etc. | 9/14/2020 |
| 609 | Foundation Medicine Cambridge, MA Molecular Technologist I BS in a science Exp: 1+ year(s) |
The Molecular Technologist I performs procedures in a complex patient sample testing process with limited supervision. Most prominently, the position is responsible for solution and reagent preparation, equipment maintenance, and the handling and testing of patient specimens. The incumbent works one of three established shifts and may be assigned to work any day that the lab is operational. Key Responsibilities: Prepare the Next Generation Sequencing (NGS) library. Under limited supervision of senior lab personnel and in adherence to established Standard Operating Procedures (SOPs): Extract and isolate nucleic acids. Complete hybridization capture, and genetic sequencing methods. Operate automated 8-span and 96-head liquid handling platforms. etc. | 9/14/2020 |
| 610 | Foundation Medicine Cambridge, MA Histotechnician (Contract) AS/AA Exp: 1+ year(s) |
The Histotechnician performs routine testing in FMI’s high complexity clinical diagnostic laboratory and is responsible for receipt of patient samples as well as the preparation of samples for microscopic examination and analysis by Pathology. This role focuses on cutting, mounting, staining, and batching slides. Key Responsibilities: Operate a microtome to produce slides or curls from paraffin blocks. Prepare and initiate samples for nucleic acid extraction. Manage sample movement through lab facilities. Ensure and maintain molecular safe integrity and quality of the specimens. etc. | 9/14/2020 |
| 611 | Foundation Medicine Cambridge, MA Bioinformatics Scientist I MS in biochemistry, bioinformatics, computer science, or related Exp: 1+ year(s) |
The Scientist I, Bioinformatics develops novel methods for detecting, reporting and analyzing alterations in tumor DNA and RNA, while optimizing existing methods. The incumbent provides scientific and technical contributions for a designated project on an interdisciplinary team. The Scientist I, Bioinformatics is also responsible for supporting novel biomarker and companion diagnostics development by mining and analyzing various types of data generated during the product development and validation process. etc. | 9/14/2020 |
| 612 | Foundation Medicine Morrisville, NC Accessioning Technician II BS/BA Exp: 0-1+ year(s) |
The Accessioning Technician II performs critical sample receipt and data entry functions in FMI’s CLIA-certified clinical laboratory. Specifically, the Accessioning Technician II receives incoming samples and ensures that necessary information has been received to move forward with processing. The Accessioning Technician II is assigned to one of three shifts and may be assigned to work any day that the lab is operational. This is a regulated position and additional information may be available from FMI Quality Assurance regarding regulatory guidelines. etc. | 9/14/2020 |
| 613 | Fresenius Kabi Melrose Park, IL Associate Chemist (1st Shift) BS in chemistry Exp: 0-3 years |
Responsible for the chemical analysis of raw material, in-process, stability and finished products as required for QC. Effectively communicates work and results both orally and in writing. PRINCIPAL ACTIVITIES PERFORMED BY THE INCUMBENT: Performs accurate routine chemical testing, such as wet analysis, assays, water testing and physical testing in full compliance with company directed SOP’s. Reviews SOP’s for applicability and notifies supervisor for necessary changes when needed. Maintains accurate records of all work performed with respect to a given project. Meets facility audit as well as cGMP or GLP requirements. etc. | 9/14/2020 |
| 614 | Fresenius Kabi Melrose Park, IL Validation Engineer BS/BA in science or engineering Exp: 1-3 year(s) |
We currently have an opportunity for a Validation Engineer in our Melrose Park Pharmaceutical Manufacturing facility who will provide technical support to operations with equipment/system/process initial validation and equipment/system/process requalifications. This is a first shift position. Weekends and off-shift hours are periodically required. Responsibilities: Schedules and executes equipment requalifications per Standard Operating Procedures (SOPs). Coordinates and communicates all testing with affected functional groups and evaluates test results. Assembles and composes the final report and circulates for approval. Executes validation studies (utility, equipment, cleaning, process, computer, and new products) to include protocol preparation, scheduling, protocol execution, and final report preparation. etc. | 9/14/2020 |
| 615 | Fresenius Kabi Wilson, NC Project Engineer BS in engineering Exp: 1-3 year(s) |
This position is responsible for procurement, design and integration of equipment, process systems and corresponding utilities. Leads the project from initial design studies to final validation, and maintains project schedule and budget while communicating results to all stakeholders. PRINCIPAL ACTIVITIES PERFORMED BY THE INCUMBENT: Conducts accurate Engineering Studies to develop design space, used for manufacturing construction, process development, equipment procurement and validation master plan. Develops and manages site projects by employing past experience, research, design and concept sketches, layouts, drawings, vendor interaction, preparation of specifications, discussions with appropriate management and site personnel. etc. | 9/14/2020 |
| 616 | Fresenius Kabi Melrose Park, IL Associate Scientist (Night Shift) BS in a biological science Exp: 1-2 year(s) |
Responsible for performing routine testing of in-process and finished product samples. Monitors environmental conditions in the production and lab areas. Summarizes environmental monitoring and product test results. Provides project support to Scientist and Lead Scientist. Prepares media and reagents and equipment. Responsibilities: Generates new standard operating procedures for microbiology test procedures. Keeps others current as assigned. Performs environmental monitoring for Skan isolators and routine testing of in-process and finished products. Assists Scientist / Lead Scientist with test method validations and special projects. Carries out special projects independently as required and assigned by supervision. Assists with plant equipment requalifications as directed. etc. | 9/14/2020 |
| 617 | Fresenius Kabi Melrose Park, IL Aseptic Filling Operator I (Day Shift) HS diploma or equivalent Exp: 1-2 year(s) |
Responsible for setting up, operating and monitoring fill equipment per Standard Operating Procedures and current Good Manufacturing Practices. Must be knowledgeable of and practice good aseptic technique to minimize potential for product contamination. Principal Activities Performed By The Incumbent: Practices aseptic technique at all times while working in aseptic areas. Complies with current SOP’s and cGMPs. Maintains aseptic gowning requirements. etc. | 9/14/2020 |
| 618 | Fresenius Kabi Melrose Park, IL Quality Inspector I (Day Shift) HS diploma or equivalent Exp: 1-3 year(s) |
Responsible for visually inspecting filled product off the filling line following Standard Operating Procedures (SOP) and current Good Manufacturing Processes (cGMP). The production inspector will work in the Capping Department and on the off-line inspection area and therefore must be knowledgeable of procedures and equipment in each area. Responsibilities: Principal Activities Performed By The Incumbent: Visually inspects products for various defects. Documents work accurately and timely. Complies with current SOP’s and cGMP’s. Sets-up, adjusts, and operates equipment such as inspection machines, cappers, etc. | 9/14/2020 |
| 619 | Fresenius Kabi Melrose Park, IL Quality Inspector I (Night Shift) HS diploma or equivalent Exp: 1-3 year(s) |
Responsible for visually inspecting filled product off the filling line following Standard Operating Procedures (SOP) and current Good Manufacturing Processes (cGMP). The production inspector will work in the Capping Department and on the off-line inspection area and therefore must be knowledgeable of procedures and equipment in each area. Responsibilities: Principal Activities Performed By The Incumbent: Visually inspects products for various defects. Documents work accurately and timely. Complies with current SOP’s and cGMP’s. Sets-up, adjusts, and operates equipment such as inspection machines, cappers, etc. | 9/14/2020 |
| 620 | Freudenberg Baldwin Park, CA Quality Specialist - Process Monitoring and Material Release BS Exp: Not necessary for BS candidates |
Your tasks: Complete all incoming/raw material and component inspections, to include verifying all documentation, and properly identify/release those materials in ERP. Perform inspection and verification of incoming materials, to include subcomponents and molded parts that have undergone off-site processing such as laser etch coatings, etc. Supports in the review and disposition of raw material, in-process and finished goods to include (NCMR/sNCMR/Material Hold Quality Notifications), departmental training/cross-training, Coordinates and monitors calibration requirements of test, measurement, and diagnostic equipment (TMDE). Administers assignment of new TMDE asset numbers, calibration requirements, calibration frequencies, and their control. Generates and investigates non-conformance reports (OOT’s – Out of Tolerance Reports) when TMDE is found to be out of calibration or missing calibration interval. etc. | 9/14/2020 |
| 621 | Freudenberg Baldwin Park, CA Maintenance Technician - 1st Shift HS diploma or equivalent Exp: 1-3 year(s) |
Your tasks: Maintaining and repairing the physical structure of the building, grounds, injection molding machines and auxiliary equipment. Painting and performing structural repairs to masonry, woodwork, and furnishings of buildings. General cleaning and up keep of buildings, including buffing, dusting, sweeping, mopping, vacuuming, and washing windows. Assist other departments as requested, including moving furniture, unloading, and storing supplies. Perform preventative and corrective maintenance on assigned equipment. Diagnose and repair electrical, hydraulic, and pneumatic control system problems on production machinery, auxiliary equipment and fixtures. Plan, layout and install electrical, hydraulic, and pneumatic systems in support of the fabrication and installation of new equipment and fixtures. etc. | 9/14/2020 |
| 622 | Frontage Exton, PA Associate Scientist, Analytical Services-CMC BS in chemistry Exp: 1-2 year(s) |
Responsibilities: 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 studies. etc. | 9/14/2020 |
| 623 | Frontage Exton, PA Scientist MS in biology, biotechnology, or related Exp: 6 months |
For a contract research organization (Frontage Laboratories, Inc. – Exton, PA): design/develop method transfer, method development, validations, quantitation and structure elucidation; perform high-volume bio-analytical sample analysis; perform data analysis, data quality control (QC) and data interpretation for bio-analytical, PK, PD and ADME studies in regulated environment; utilize and maintain analytical instruments, including Liquid Chromatography Tenderm Mass Spectrometry (LC-MS/MS) and Nuclear Magnetic Resonance (NMR); perform technical work related to the care and use of research animals. etc. | 9/14/2020 |
| 624 | Frontage Exton, PA Associate Scientist-Product Development- CMC MS in pharmaceutical sciences, polymer chemistry, microbiology, or chemical engineering Exp: 0-4 years |
Responsibilities: Perform assigned tasks per procedures compliant with cGMPs and participate in the clinical manufacturing of parenteral, ophthalmic, and other sterile dosage forms. Participate in media fills for aseptic fill projects. Assist in the equipment set up, operation, maintenance, cleaning as required for the project. Perform Environmental Monitoring (EM) of manufacturing areas per applicable SOPs and maintain records. Assist with manufacturing area maintenance such as area monitoring and qualification, purchase of gowning supplies, purchase of equipment and room cleaning supplies, microbiological monitoring supplies. Maintain records for personnel gowning qualification. etc. | 9/14/2020 |
| 625 | Frontage Exton, PA Scientist-002 MS in biology, biomedical science, or related Exp: 1 year |
Job Duties: Conduct in vitro and in vivo metabolism studies using radiolabeled and non-radiolabeled compounds. Conduct bioanalytical assays using HPLC and LC/MS/MS. Use LSC and sample oxidizers to generate data for radioactive mass balance studies. Develop sample analysis method and perform metabolites identification. Isolate and identify radioactive and non-radioactive metabolites from in vivo and in vitro. Provide routine animal care and perform technical work related to the care and use of research animals. Maintain mammalian and primary cell lines for preclinical experiments. Perform work in regulated environment. etc. | 9/14/2020 |
| 626 | Frontage Exton, PA Scientist- Bioanalytical Services-ICP-MS MS in analytical chemistry, biochemistry, pharmacology, or related Exp: 1+ year(s) |
Scientist / Bioanalytical Services Essential Functions Run sensitive, reliable and efficient LC-MS/MS bioanalytical assays for TK/PK assessment. Candidates with experience in ICP-MS and/or ICP-MS/MS for bioanalytical or other applications are preferred. Duties: Perform high-volume sample analysis and/or data analysis, data QC, and data interpretation. Maintain schedule of projects and timelines. Coordinate study activities with Principle Investigator to ensure efficiency and quality. Aid in the preparation of study summaries and/or reports. etc. | 9/14/2020 |
| 627 | Frontage Spring House, PA Scientist-STE Assay Development MS in biology, chemistry, biochemistry, or related Exp: 1-2 year(s) |
This laboratory-based position is in the Soluble Target Engagement (sTE) Assay Development group within the Bioanalytical Sciences department. Develop assays to quantify biopharmaceutical drug targets in various sample matrices from non-clinical and clinical studies; Perform and interpret complex in vitro, ex vivo and in vivo experiments with some independence; Analyze and present data in professional format; Demonstrate clear and professional verbal and written communication; Conduct, analysis and reporting of data in accordance with requirements set forth by the department; Ensure maintenance of detailed documentation of assay development and qualification; Record experimental data and accurate and highly organized laboratory notebooks; Follow appropriate SOPs and all internal documentation requirements. etc. | 9/14/2020 |
| 628 | Frontage Exton, PA Scientist-PK/ADA BS/MS in a biology related field Exp: 1-2 year(s) |
Performs biologics method transfer, method development and validation according to FDA guidance, Frontage SOP and industry practices. Performs sample analysis following SOPs and methods, prepare, review the data package and reports. Provide training and technical guidance to the junior scientists. Provide assistance to project management to ensure meeting the requirements of project quality, and timelines. Provide assistance to the PI/RS to ensure the compliance. etc. | 9/14/2020 |
| 629 | Fujifilm Diosynth College Station, TX Manufacturing Technician I/II AS in biology, microbiology, chemistry, engineering, or related Exp: 0-1+ year(s) |
Essential Functions Include: 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. etc. | 9/14/2020 |
| 630 | Fujifilm Diosynth College Station, TX Manufacturing – Associate Process Engineer BS in science, engineering, or related Exp: 1 year |
Develop and maintain equipment and unit operation standards and procedures utilizing 4M (Man, Materials, Machinery and Methods) approach including: Support new equipment purchasing, URS creation and or revision, equipment qualification and procedure creation and or revision. Creation and or revision of recipe or methods for various platforms. Review and/or Approve equipment qualification limits. Review Calibration Tolerances and Approve Out of Tolerance Investigations. Develop and approve procedures for new equipment being introduced into the plant. Support new product transfer by creation or revision of the Process Consumable List. etc. | 9/14/2020 |
| 631 | Fujifilm Diosynth College Station, TX Maintenance Technician I – Night Shift AS/AA in engineering, maintenance, bioengineering, or related Exp: 1 year |
Essential Functions: Provide maintenance and operational support for clean utility equipment such as clean gases, steam generated Water for Injection (USP), clean steam systems, and RODI water systems. Provide maintenance and operational support for plant utility equipment, including utilities such as air compressors, air dryers, steam boilers, chillers, heating hot water boilers, HVAC systems and waste disposal systems. Provide maintenance and operational support for facilities, building maintenance and grounds. Technician will assist senior technician on critical environment controls, maintenance on critical laboratory equipment within GMP clean rooms and environmental controlled areas. Able to work with operators and technicians in helping to perform troubleshooting tasks on temperature controlled process equipment, such as bioreactors, centrifuges, micro-filtration skids, and autoclaves. etc. | 9/14/2020 |
| 632 | Fujifilm Diosynth College Station, TX Facilities Engineer I BS in electrical, chemical, mechanical, or biomedical engineering Exp: 1 year |
Essential Functions: Responsible for providing engineering, operational and troubleshooting support to facilities, utilities and process equipment as needed. Responsible for monitoring complex equipment and maintaining the equipment with a minimum of downtime. Responsible for developing, writing, editing and/or reviewing SOPs, JHAs, HECPs, P&IDs and operations/maintenance procedures for facilities, utilities and process equipment. Responsible for the implementation of process improvements and corrective actions as well as the development of maintenance strategies and equipment life cycle. Responsible to support equipment IQ/OQ/PQ or any other validation startup activity as required. Responsible to support Reliability Centered Maintenance (RCM) activities including condition monitoring and predictive technologies as applicable. etc. | 9/14/2020 |
| 633 | Fujifilm Diosynth College Station, TX Drug Product Operations – Technician III MS in biology, microbiology, chemistry, engineering, or related Exp: 1 year |
Essential Functions: Responsible for the operation of Vanrx SA25 Vial Filling Isolator. Responsible for assisting in the formulation of the bulk drug product in accordance to procedures. Responsible for visual inspection and labeling of filled bulk drug product vials in accordance to procedures. Assist in writing, reviewing, and/or updating Standard Operating Procedures (SOPs) and Batch Production Records (BPRs). Document and maintain activity records according to cGMP regulations and ensure junior team members are trained. Help implement project safety and quality assurance programs in collaboration with senior staff and EH&S. etc. | 9/14/2020 |
| 634 | Immunomic Therapeutics Rockville, MD Process Development Associate I-II MS in sciences Exp: 0-1 years |
Reporting to the Sr. Manager, Process Development, this position will be responsible for the upstream processes used in nucleic acid vaccine production including bacterial transformation and fermentation. Incumbent will become proficient in other areas including plasmid purification, transient transfection, and Western blotting in support of the Process Development (PD) laboratory at ITI. | 8/29/2020 |
| 635 | Immy Norman, OK Quality Assurance Technician I Associates in science or engineering Exp: 0-2 years |
Under moderate supervision, the Quality Assurance Technician I is responsible for performing all monthly, quarterly, and yearly calibrations of laboratory equipment, maintaining equipment lists, performing quality inspections on incoming items, and manufacturing materials needed to support the Quality Management System. | 8/29/2020 |
| 636 | Immy Norman, OK Medical Records Technician Associates in sciences or Med Lab technician certification Exp: 1-2 years in lab |
The purpose of this position is to support IMMYLabs in clerical duties in a manner that is consistent with medical, administrative, legal, and regulatory requirements. This position will process, maintain, compile, and report information in a standard manner consistent with all reporting agreements. | 8/29/2020 |
| 637 | Immy Norman, OK Upstream Technician BS/BA in biological sciences Exp: 0-2 years in lab |
The Upstream Technician is responsible for the manufacture of immunoassays. This includes buffer manufacturing, testing, and manipulation for all products lines (LFA, EIA, Complement Fixation, Latex Agglutination, and Immunodiffusion). This person will perform various types of conjugations, quantifications, purifications, and antigen/antibody pairing and must have a high attention to detail. Upstream Technicians will be trained to excel in one product line before training in another. | 8/29/2020 |
| 638 | Immy Norman, OK Systems Analyst Degree or pursuing a degree in IT related field Exp: 0-1 years |
The systems analyst helps support, validate, maintain, and test software and other technology systems. This position participates in design and testing activities with other staff members. | 8/29/2020 |
| 639 | Immy Norman, OK PCR Specimen Processing Technician HS Diploma/GED, AA or BS/BA, or MT/MLT certification Exp: 1-2 years in lab |
The primary responsibility of this position is to handle incoming samples for accessioning, organizing, storing, and processing. Processing of samples will include DNA isolation of various sample types, prep for PCR and running PCR testing. | 8/29/2020 |
| 640 | Impulse Dynamics Pearl River, NY Regulatory Affairs Specialist BS/BA or MS in regulatory affairs Exp: 0-3 years |
Participate in preparation and submission of regulatory submissions to obtain approval to conduct domestic and international clinical investigations and to seek regulatory approval to commercialize the new and existing devices and their accessories. (IDE supplements, PMA, Annual reports, change notice etc) | 8/29/2020 |
| 641 | InBios Seattle, WA Manufacturing Associate I - ELISA BS/BA in life sciences or Associates in applied sciences Exp: BS/BA: 0 years, Associates: 1 year |
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. | 8/29/2020 |
| 642 | Incyte Wilmington, DE Research Scientist, Biologics Analytical Sciences BS/BA or MS in sciences/engineering Exp: 1-3 years for analytical development for biologics |
Reporting to the analytical chemistry lead this position will be responsible for designing and conducting experiments to develop new analytical methods to support release testing, stability, and characterization of a growing biologics pipeline. This role requires scientific knowledge of a variety of analytical methods, experience in biologics development from early stage to late stage, and familiarity with ICH guidance. Strong interpersonal and communication skills are required. | 8/29/2020 |
| 643 | Indivior Houston, TX Specialty Pharmaceutical Sales Rep/Clinical Specialist (Houston - North) BS/BA Exp: 1+ years in pharma/medical/healthcare |
The Clinical Specialist must provide the healthcare professional with the most current information pertaining to Indivior products and their approved indications in a manner which will ensure the appropriate use of these products and achieve the business potential of the territory. | 8/29/2020 |
| 644 | InGeneron Houston, TX Quality Assurance Specialist BS/BA in biological sciences or engineering Exp: 0-3 years |
The Quality Assurance Specialist is responsible for providing Quality Assurance, Quality Control, and Preventative activity support for InGeneron’s Quality Management System. The Quality Assurance Specialist supports operations and other business functions with a focus on compliance to FDA and global quality system regulations and standards. | 8/29/2020 |
| 645 | Innogenix Amityville, NY Quality Control Chemist MS in chemistry or related Exp: 1 year in QC |
Perform quality control/development activities. Develop, validate and test analytical methods. Analyze raw materials, in-process and finished product samples using modern QC techniques and advanced analytical equipment. Assist Scientists in developing/implementing quality systems and activities. | 8/29/2020 |
| 646 | Inova Diagnostics San Diego, CA Research Associate I BS/Ba in biological sciences Exp: 1-2 years in research |
This position assists in the development of current and future Inova Diagnostic product lines by performing laboratory activities to assist in the development of new assays and/or the identification of potential new biomarkers. This position works under the supervision of the R&D management team and 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. | 8/29/2020 |
| 647 | Inova Diagnostics San Diego, CA Chemist I - Elisa Plates BS/BA in biological or chemical sciences Exp: 0-2 years in lab |
Assists with preparation of ELISA and Luminex™ plates according to established procedures. Major duties include assistance with reagent formulation, filtration and ELISA Plate Manufacturing activities. Assists with preparation of antigen solutions and buffers for ELISA plates according to written manufacturing documents. | 8/29/2020 |
| 648 | Inova Diagnostics San Diego, CA Customer Service Representative I HS Diploma/GED Exp: 0-1 years |
Assists with answering phones and the processing of orders. Assists in answering the telephone. Assists Quality Assurance (QS) and Marketing with various projects. Assists in the processing, double checking and obtaining confirmation of sales orders. Assists in the preparation of paper work for the shipment of sales orders domestic and foreign | 8/29/2020 |
| 649 | INOVIO San Diego, CA Associate, Quality Assurance (Laboratory) Associates or BS/BA Exp: 1-2 years in quality |
The Quality Assurance (QA) Associate (Laboratory) has the primary responsibility for supporting QA activities along with supporting Quality Systems and compliance as needed. The QA Associate performs a wide variety of duties, including supporting the daily QA Bioanalytics (laboratory) departmental operations, aiding with study protocol and report oversight, performing audits (internal/external) and performing various types of documentation reviews for applicable programs involving Inovio studies. | 8/29/2020 |
| 650 | INOVIO San Diego, CA Research Associate I (Temporary/Contractor) BS/BA in biological sciences Exp: 0-1 years in lab |
The Research Associate I (RAI) works under general and specific direction in performing a spectrum of techniques in both cell culture and immunology. The RAI works collaboratively and independently in the lab, solves problems, completes required documentation, and performs general lab duties. | 8/29/2020 |
| 651 | ConforMIS Wilmington, MA CNC Machinist, 1st Shift HS diploma or equivalent Exp: 1-3 year(s) |
The CNC Machinist I will be responsible for operation of CNC machining centers and polishing of medical implants in a high-volume manufacturing environment. Essential Duties and Responsibilities: Develop and maintain strong internal working relationships across Conformis. Understand the objectives, responsibilities, and mission of the operations department and work towards those goals. Prioritize and plan work activities; adapt for changing conditions. Operation and light maintenance of CNC machining centers and associated tooling. Perform hand de-burring of metal medical implants after machining. Perform in-process inspection of CNC machined parts. Perform timely and accurate transactions of workflow in ERP system. Maintain CNC machine spare parts and consumable tooling. etc. | 9/7/2020 |
| 652 | Contract Pharmacal Corp Hauppauge, NY QA Manufacturing Coordinator AS/AA/BS/BA Exp: 1 year |
The QA Manufacturing Coordinator has primary responsibility for handling all front office operations as outlined below. Responsibilities: Including but not limited to: Track Change Controls and Deviations that affect manufacturing particularly those that affect MMR(s) and batch records. Change control assignee within Master Control all CC throughout all departments. Coordinate the bulk label process including creation, customer approval and maintenance. Liaison between Coating and QC, reporting batches completed through compression. Perform check of all issued batches to Manufacturing. Review issued commercial batches for coating material needs/maintain Coating Batch Log. Review of various Manufacturing systems (e.g. pest control, purified water). etc. | 9/7/2020 |
| 653 | Cook Group West Lafayette, IN Research Engineer BS in engineering Exp: 1-5 year(s) |
The Research Engineer at Cook Research Incorporated is responsible for completing project deliverables and tasks to support the evaluation of novel design concepts for new medical products and providing support to projects in development at Cook Group companies. The successful candidate will support research and development of novel medical devices supporting the MedSurg Division for Cook. This candidate will also be expected to work with a project team to identify clinical needs, formulate new concepts, produce prototypes, conduct feasibility assessments and produce documentation for designs. Familiarity with a variety of medical device materials would be advantageous. etc. | 9/7/2020 |
| 654 | Cook Group Poway, CA Machine Operator HS diploma or equivalent Exp: 6 months |
The Machine Operator at K-Tube Technologies will be skilled in operating machinery in one or more departments of Weld, Plug, Sink, Straightening, Cutting, Chop Cut, and CG. Knowledgeable in performing set ups in accordance with established procedures. Trained in the proper use of tooling for small, medium or large gauge sizes. Will also be responsible for the maintenance of all tooling used in manufacturing. Instructed in sampling procedure and inspection techniques on measuring the OD, using OD gauge and pin gauge for measuring ID. Must be certified to operate a machine and sign off on production. Performs process checklist and sampling procedure. etc. | 9/7/2020 |
| 655 | Cook Group Pittsburgh, PA Equipment Associate HS diploma or equivalent Exp: 1-3 year(s) |
The Equipment Associate at Cook MyoSite assists in supporting company operations by monitoring and controlling laboratory equipment and production related utilities, as well as assisting with facility related aspects of equipment and the quality system. Responsibilities: Perform the proper receiving, tracking and storing of purchased equipment. Organize and maintain a calibration schedule for equipment. Ensure that all measuring and test equipment used is registered, assigned and marked with a unique internal equipment number for identification. Organize files and maintain all laboratory equipment and facility records. Maintain a calibration schedule utilizing calibration database software. etc. | 9/7/2020 |
| 656 | CRISPR Therapeutics Cambridge, MA Research Associate, Genomics BS in biology or related Exp: 1+ year(s) |
We are seeking a Research Associate to join our next generation sequencing (NGS) wet lab. The successful candidate will be responsible for performing quality control experiments and generating NGS data to support the development of novel genetic therapies for a serious diseases. This position requires enthusiasm, attention to detail, and a desire to create new medicines for patients. This position reports directly to the head of the NGS wet lab. General Responsibilities: Perform routine quality control experiments on sequencing libraries (fluorescent quantification, capillary electrophoresis, and qPCR) and prepare samples for sequencing. Load and operate Illumina sequencers. Apply operational knowledge of instruments used in the genomics space (e.g. TapeStation, Bioanalyzer, optical plate reader, robotic liquid handling, and Illumina sequencers). etc. | 9/7/2020 |
| 657 | CSL Dallas, TX Plasma Lab Technician HS diploma or equivalent Exp: 3+ months |
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors. In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. Ensures accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. May ensure samples and units are packed and shipped in accordance with SOPs and center procedures. Prepares shipping and unit disposal documentation. etc. | 9/7/2020 |
| 658 | CSL New Hope, MN Customer Service - Donor Support Technician HS diploma or equivalent Exp: 3+ months |
Responsible for preparing the donor, donor area and equipment for the pheresis process. Job Description: Main Responsibilities: Prepares the autopheresis machine for the pheresis process. Monitors the donor and the pheresis process, responds to specific alarms or signals that may occur during the process. Disconnects the donor when the process is complete. Maintains alertness and awareness to any reaction donor may have during or after the pheresis process and notifies appropriate staff. Uses Personal Digital Assistant (PDA) to record incidents that occur during the pheresis process, such as machine alerts and alarms, volume variances and donor adverse events. etc. | 9/7/2020 |
| 659 | CSL Burlington, NC Medical Screener - Reception Technician (Customer Service) HS diploma or equivalent Exp: 3+ months |
Responsible for greeting donors at the plasma collection center and conducting a series of registration procedures to verify donor suitability for the plasma pheresis process. In compliance with Standard Operating Procedures (SOPs), assists qualified donors in completing the screening process. The screening procedures includes but are not limited to: assessing the self-administered health history, answering basic medical questions associated with the donation process, referring donors to medical staff when appropriate and performing health screening procedures such as blood pressure, pulse, weight, temperature. Performs finger stick to obtain sample to obtain donor’s hematocrit and total protein levels. etc. | 9/7/2020 |
| 660 | CSL Madison, TN Medical Screener - Reception Technician (Customer Service) (Bilingual – English/Spanish) HS diploma or equivalent Exp: 3+ months |
Responsible for greeting donors at the plasma collection center and conducting a series of registration procedures to verify donor suitability for the plasma pheresis process. In compliance with Standard Operating Procedures (SOPs), assists qualified donors in completing the screening process. The screening procedures includes but are not limited to: assessing the self-administered health history, answering basic medical questions associated with the donation process, referring donors to medical staff when appropriate and performing health screening procedures such as blood pressure, pulse, weight, temperature. Performs finger stick to obtain sample to obtain donor’s hematocrit and total protein levels. etc. | 9/7/2020 |
| 661 | CSL Manhattan, KS Customer Service - Donor Support Technician HS diploma or equivalent Exp: 3+ months |
Responsible for preparing the donor, donor area and equipment for the pheresis process. Job Description: Main Responsibilities: Prepares the autopheresis machine for the pheresis process. Monitors the donor and the pheresis process, responds to specific alarms or signals that may occur during the process. Disconnects the donor when the process is complete. Maintains alertness and awareness to any reaction donor may have during or after the pheresis process and notifies appropriate staff. Uses Personal Digital Assistant (PDA) to record incidents that occur during the pheresis process, such as machine alerts and alarms, volume variances and donor adverse events. etc. | 9/7/2020 |
| 662 | CSL Evansville, IN Medical Screener - Reception Technician (Customer Service) HS diploma or equivalent Exp: 3+ months |
Responsible for greeting donors at the plasma collection center and conducting a series of registration procedures to verify donor suitability for the plasma pheresis process. In compliance with Standard Operating Procedures (SOPs), assists qualified donors in completing the screening process. The screening procedures includes but are not limited to: assessing the self-administered health history, answering basic medical questions associated with the donation process, referring donors to medical staff when appropriate and performing health screening procedures such as blood pressure, pulse, weight, temperature. Performs finger stick to obtain sample to obtain donor’s hematocrit and total protein levels. etc. | 9/7/2020 |
| 663 | CSL Hamilton, NJ Sr Plasma Processing Technician HS diploma or equivalent Exp: 3+ months |
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors. Main Responsibilities: In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. Ensures plasma units are properly stored according to SOPs, which could include unsuitable plasma units and samples. May ensure accuracy of unit labeling by verifying the pre-printed label matches the dynamic label. etc. | 9/7/2020 |
| 664 | Cutis Pharma Woburn, MA Quality Control Chemist--Entry Level BS/BA Exp: 0-1 year(s) |
The QC Chemist will be responsible to perform assigned tasks accurately, following approved documents, Azurity Pharmaceuticals procedures and policies, Good Documentation Practices, and Good Analytical Laboratory Practices. PRINCIPAL DUTIES AND RESPONSIBILITIES: Perform analytical testing of API and finished products. Instrumental analysis and wet chemistry. Demonstrate familiarity with standard QC lab equipment. Independently collect, analyze, and interpret data and recognize aberrant results. Maintain good housekeeping in QC Lab. etc. | 9/7/2020 |
| 665 | Cutis Pharma Wilmington, MA Quality Line Inspector BS/BA in chemistry or a life science Exp: 1-3 year(s) |
DUTIES & RESPONSIBILITIES: Inspect all incoming component shipments to ensure that all applicable specifications are met. Inspect product shipments coming from contract manufacturers/repackagers to ensure that all necessary components meet quality standards. Help trouble-shoot packaging concerns and communicate with contract manufacturers/ repackagers and vendors. Verifies and inspects incoming materials and works accordingly with Quality Assurance to handle any possible discrepancies. Participates in other quality audits when required. Complete and maintain documentation of all items inspected and findings/conclusion of findings. Provide oversight on production line; assist Production Technicians with questions/inquiries about products. etc. | 9/7/2020 |
| 666 | Cytek Biosciences Fremont, CA Research Scientist I BS/MS in a life science Exp: 1-2 year(s) |
We are seeking a motivated candidate who can assist in new reagent, assay, and system development and testing. The candidate should be able to execute experiments and testing independently following protocols or instructions. In addition, the candidate should have good communication, documentation and problem-solving skills. Primary Responsibilities: Follow instructions to carry out flow cytometry experiments using biological samples. Follow SOPs and protocols to carry out reagent, assay panel, and instrument testing. Perform data analysis and summarize data for review. Design experiment to trouble shoot if necessary. etc. | 9/7/2020 |
| 667 | Cytek Biosciences Columbus, OH Flow Cytometry Field Service Engineer BS in a life science or engineering Exp: Not required |
DUTIES AND RESPONSIBILITIES: Install, troubleshoot and repair flow cytometers and Cytek Upgrade products with proficiency in a timely manner. Work professionally and courteously as an individual with Cytek’s customers in continuous support of Cytek’s reputation of service excellence. Identify customer needs and contribute to improvements in Cytek products. Manage the daily schedule to ensure appropriate priority is placed upon urgent customer needs while setting customer expectations for issues of less urgency. Customer Management through telephone technical support, service visit scheduling, product problem information gathering, fault isolation, corrective action, and site visit closure with high quality and efficiency. etc. | 9/7/2020 |
| 668 | Cytek Biosciences Seattle, WA Flow Cytometry Field Service Engineer BS in a life science or engineering Exp: Not required |
DUTIES AND RESPONSIBILITIES: Install, troubleshoot and repair flow cytometers and Cytek Upgrade products with proficiency in a timely manner. Work professionally and courteously as an individual with Cytek’s customers in continuous support of Cytek’s reputation of service excellence. Identify customer needs and contribute to improvements in Cytek products. Manage the daily schedule to ensure appropriate priority is placed upon urgent customer needs while setting customer expectations for issues of less urgency. Customer Management through telephone technical support, service visit scheduling, product problem information gathering, fault isolation, corrective action, and site visit closure with high quality and efficiency. etc. | 9/7/2020 |
| 669 | Cytovance Biologics Oklahoma City, OK SOLUTION PREP ASSOCIATE AS/AA in a life science Exp: 1-2 year(s) |
This position is accountable for producing and delivering large and small-scale media and buffers to support Upstream and Downstream Manufacturing Operations. ESSENTIAL DUTIES AND RESPONSIBILITIES: Batching and delivering both large and small-scale media and buffer batches. Assisting in the review & creation of operation documents by providing input to technical composition of documents. Effectively demonstrate understanding of GMPs & how it applies to specific responsibilities. Following accurate oral & written procedures in operating production equipment & performing processing steps. Maintain orderliness of process area. etc. | 9/7/2020 |
| 670 | Cytovance Biologics Oklahoma City, OK MANUFACTURING ASSOCIATE - UPSTREAM - NIGHT SHIFT AS in science or biotechnology Exp: 1-2 year(s) |
Executes upstream manufacturing of clinical and commercial products. Executes pre and post processing activities such as: clean of production equipment, including the operation of automated bioreactor, harvest and media prep skids. This position is accountable for executing the manufacturing processes in Contract Manufacturing Facility and/or Master Cell Banking Facility. ESSENTIAL DUTIES AND RESPONSIBILITIES: Ability to work with bioreactor operation and cell culture including aseptic technique. Execute and monitor critical processes supporting mammalian, microbial, and fill finish production facilities. Solid experience with the following: large-scale centrifuges, washers, autoclaves. etc. | 9/7/2020 |
| 671 | Cytovance Biologics Oklahoma City, OK MANUFACTURING ASSOCIATE - DOWNSTREAM AS in science or engineering Exp: Not necessary for AS candidates |
This position is accountable for the execution of procedures for purification manufacturing and support area of manufacturing using SOP’s and batch records. Operating production equipment for purification that may include process monitoring, purification and formulation. ESSENTIAL DUTIES AND RESPONSIBILITIES: Perform in-process testing where applicable. Interface with Quality Control department to submit in-process samples and coordinate environmental monitoring during key process steps. Provide support to cross-functional teams to meet production or timeline demands. Demonstrate understanding in scientific concepts, technical operations, safety, and Good Manufacturing Practice. Provide suggestions for process optimization and efficiency, where applicable. etc. | 9/7/2020 |
| 672 | Day Zero Diagnostics Boston, MA Laboratory Research Associate BS in molecular biology, biochemistry, or microbiology Exp: 1 year |
Job Duties: Perform and assist with sample processing toward diagnostic workflows. Ensure quality control of equipment, reagents, and clinical samples. 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. etc. | 9/7/2020 |
| 673 | Demetrix Berkeley, CA Associate Scientist/Sr. Associate Scientist - Analytical Chemistry BS in chemistry, biochemistry, chemical engineering, or related Exp: 1 year |
You will be part of an interdisciplinary team of fermentation scientists and engineers, automation engineers, software engineers, analytical chemists, and molecular biologists to rapidly develop microbial strains to produce high value natural product medicines. The Analytical Chemistry group is an integral part of the Demetrix team, providing the rest of the company with high quality data while maintaining and balancing accuracy, precision, and throughput. As part of the Analytical Chemistry group, you will help us with operations, instrument maintenance and troubleshooting, and development of new methods while fostering an atmosphere of continued improvement and innovation. etc. | 9/7/2020 |
| 674 | Dexcom San Diego, CA Engineering Technician 1 HS diploma or equivalent Exp: 0-2 years |
As a member of the R&D Advanced Technology team this Technician will support efforts to understand current and future needs of our manufacturing and automation processes, explore and evaluate new technologies and concepts for meeting those needs, and assist in rapidly demonstrating feasibility of such technologies through rigorous modeling, analysis, prototyping, experimentation, and other risk identification and mitigation activities. Functional Description: Supports engineering activities such as design, test, check-out, modification, fabrication and assembly of prototype electro mechanical systems, experimental design circuitry, laser/light transmission devices or specialized test equipment. Applications may include electronic circuits, photonics and logic systems. etc. | 9/7/2020 |
| 675 | Dyne Therapeutics Waltham, MA Research Associate/Senior Research Associate - Biology BS/MS in a biological discipline Exp: 1-2 year(s) |
Dyne is seeking a talented and highly motivated Research Associate/Senior Research Associate to join our drug discovery team. This member will work closely with other researchers to develop biomarker assays using a variety of innovative technologies. The successful candidate will be ambitious, motivated, an energetic self-starter who enjoys working in a fast-paced environment. We offer a competitive salary with benefits and an opportunity for learning and advancement in an exciting innovative environment. Primary Responsibilities Include: Execute research plans for in vitro/in vivo studies. Analyze data and communicate findings to team members and management. etc. | 9/7/2020 |
| 676 | Holologic San Diego, CA Research Associate 2 BA/BS in molecular biology, chemistry, or biochemistry Exp: 0-2 years |
Hologic is seeking a Research Associate 1 or 2 responsible for designing and performing experiments while collaborating and communicating effectively. Essential 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 minimally complex experiments with input from supervisor. Understands experimental goal and may provide input to the experimental design. Analyzes data from individual experiment with input from supervisor and documents work in laboratory notebook or report. Able to summarize a group of experiments. Effectively communicates with peers and supervisor. May present data in group meetings. etc. | 9/7/2020 |
| 677 | Holologic San Diego, CA Research Associate 1 or 2 BA/BS in molecular biology, chemistry, or biochemistry Exp: 0-2 years |
Hologic is seeking a Research Associate 1 or 2 responsible for designing and performing experiments while collaborating and communicating effectively. Essential 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 minimally complex experiments with input from supervisor. Understands experimental goal and may provide input to the experimental design. Analyzes data from individual experiment with input from supervisor and documents work in laboratory notebook or report. Able to summarize a group of experiments. Effectively communicates with peers and supervisor. May present data in group meetings. etc. | 9/7/2020 |
| 678 | Editas Medicine Cambridge, MA Clinical Trial Assistant BA/BS Exp: 1-3 year(s) |
The Clinical Trial Assistant is an individual contributor providing clinical trial coordination support, along with implementing the clinical operational plans in accordance with regulatory guidelines and ICH/GCP standards. The Clinical Trial Assistant will be responsible for providing Clinical Operations support of study specific reports and site and vendor management activities. throughout the full lifecycle from study start-up through database archive. This includes collaboration with CROs and cross-functional teams. The position reports to the VP Clinical Science Operations and Clinical Quality. These responsibilities include: Supports the clinical team in the overall management of studies, including planning, execution and closeout of one or more clinical trials. etc. | 9/8/2020 |
| 679 | Elpis Biopharmaceuticals Lexington, MA Research Associate, Biology & Functional Assays BS/MS in biology, biochemistry, molecular biology, immunology, or related Exp: 1-3 year(s) |
We are looking for a research associate to joint the biology and functional assay group. This group will analyze and screen newly discovered therapeutic molecules for biochemical, cellular and immunological function. The candidate will be responsible for efficiently delivering high-quality research results for decision making. The candidate will also help explore and develop innovative technologies to advance biologic projects. The candidate will analyze scientific results, provide oral and written reports, and remain current to literature reports and technological developments. etc. | 9/8/2020 |
| 680 | Emergent Biosolutions Baltimore, MD Manufacturing Associate BS in biological sciences or HS diploma Exp: 1+ year(s) |
The Manufacturing Associate II position reports to Manager Manufacturing at Emergent Manufacturing Operations Baltimore (EMOB). Prior experience in GMP manufacturing and operation of GMP process equipment are prerequisites. Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions. Operates manufacturing equipment such as: incubators, single-use bioreactors, depth filtration skids, TFF skids, chromatography skids, single-use mixers and in process testing equipment. Demonstrates, understands and adheres to Emergent policies, GMP standards and safety procedures. Informs Manager on progress of projects, transfer of data, process details, etc. | 9/8/2020 |
| 681 | Emergent Biosolutions Baltimore, MD Manufacturing Associate (Upstream) BS in biological sciences or HS diploma Exp: 1+ year(s) |
The Manufacturing Associate II position reports to Manager Manufacturing at Emergent Manufacturing Operations Baltimore (EMOB). Prior experience in GMP manufacturing and operation of GMP process equipment are prerequisites. ESSENTIAL FUNCTIONS: Operates manufacturing equipment such as: incubators, single-use bioreactors, depth filtration skids, TFF skids, chromatography skids, single-use mixers and in process testing equipment. Demonstrates, understands and adheres to Emergent policies, GMP standards and safety procedures. Informs Manager on progress of projects, transfer of data, process details, etc. Executes batch records according to GMP and site quality standards. etc. | 9/8/2020 |
| 682 | Emergent Biosolutions Lansing, MI Analyst I, QC Environmental Monitoring BS in an applied science Exp: 0-2 years |
This is a laboratory testing position with the major responsibilities being daily routine testing and laboratory maintenance tasks. Additional responsibilities involve quality systems support. ESSENTIAL FUNCTIONS: Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions. Environmental Monitoring Responsibilities: Perform general laboratory duties including, but not limited to: Clean laboratory areas/glassware. Biosafety Cabinet Monthly Cleaning. Safety equipment upkeep including eyewash stations. Transfer and dispose of biohazard waste and chemicals. etc. | 9/8/2020 |
| 683 | Emergent Biosolutions Baltimore, MD Analyst II, QA Raw Materials BS/MS in chemistry or biology Exp: 1-3 year(s) |
The QA Analyst II is responsible for performing duties related to raw materials review and release for the CGMP operation of Emergent BioSolutions Emergent BioSolutions at 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. ESSENTIAL FUNCTIONS: Raw Materials: Perform critical reviews of Incoming material documentation submitted for QA disposition. Perform activities associated with the Active Pharmaceutical Ingredient (e.g. receipt, inspection and document review). etc. | 9/8/2020 |
| 684 | Encoded Therapeutics South San Francisco, CA Research Associate I/II, In Vivo Research MS in biosciences Exp: 0-2 years |
We are recruiting a highly motivated researcher to join our team. This is a unique opportunity to work at the intersection of genomics and therapeutics and participate in the development of a diverse therapeutic pipeline driven by a transformative core technology. The successful candidate will work well across multiple projects in a fast-paced and dynamic environment. Requirements: Conduct in vivo procedures to evaluate efficacy of AAV gene therapy candidates in rodent models, primarily mice. Perform standard mouse procedures including plasma/serum collection, IV injections, necropsies, and tissue collection in compliance with established protocols. Conduct in life safety assessments: monitor body weight, clinical observations, and survival of mice. etc. | 9/8/2020 |
| 685 | EntroGen Woodland Hills, CA Quality Control/Quality Assurance Associate BS/MS in molecular biology, biology, biochemistry, or related Exp: 1+ year(s) |
EntroGen is seeking a Quality Control/Quality Assurance Associate who will be responsible for routine quality control procedures under general supervision. The main responsibilities of this position include performing routine testing of raw materials, in-process samples, controls, and finished product, writing protocols and reports, compiling data into comprehensive packages, packaging and inspecting products, reviewing batch records for accuracy, assuring cGMP compliance, and writing/revising SOPs. This position will also provide support to manufacturing and production as needed. etc. | 9/8/2020 |
| 686 | Envigo Alice, TX Animal Care Technician Unspecified Exp: 6-12 months |
To assist with daily primate husbandry in accordance with SOPs and assist with maintenance of work area. How you will contribute to make a difference: Perform daily rounds to observe primates for signs of illness. Perform routine weighing of primates. Capture and restrain primates as needed. Maintain and sanitize animal enclosures. Assist with administration of medications. Perform blood collections. Perform documentation as required by operating procedures. Conduct general animal husbandry procedures. Assist in preparing and crating primates for incoming or outgoing shipments. Outside maintenance, grounds keeping. etc. | 9/8/2020 |
| 687 | Erytech Princeton, NJ Technician - Manufacturing BS in a biological science Exp: 1-2 year(s) |
Scope: Be able to manufacture human blood derived oncology drugs per Standard Operating Procedures in a controlled cleanroom environment. Ensures all manufacturing activities are performed under cGMP guide lines. Communicates production deviations/incidents to the supervisor/Manager as soon as it is discovered. Responsibilities: Ensures all training requirements are completed according to Erytech training guidelines. Perform all manufacturing activities according to cGMP guide lines. Record all manufacturing activities in the batch record and Erycaps machine according to the SOP.ng. etc. | 9/8/2020 |
| 688 | Eurofins Denver, CO Mold/Asbestos Analyst BS in microbiology, biology, geology, or related Exp: 1+ year(s) |
The Analyst primarily performs analysis of bulk samples using PLM for asbestos, and analysis of non-culturable surface and air samples for fungi. 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. etc. | 9/8/2020 |
| 689 | Eurofins West Point, PA Downstream Process Development Scientist BS in biology, chemistry, or related Exp: 0-2 years |
Employee Responsibilities: Perform lab-scale downstream processing of vaccine products and process intermediates. Perform assays on vaccine products, process intermediates, and related experimental samples using biochemical/analytical tests. Prepare solutions/reagents. Set-up process equipment for lab-scale experiments. Maintain records and experimental results following good manufacturing practices (GMP). etc. | 9/8/2020 |
| 690 | Exelixis Alameda, CA Assistant Research Scientist I BS/MS in a biological science Exp: 0-2 year(s) |
The successful and highly motivated candidate will support the clinical pharmacology and nonclinical development in PK data review and documentation in addition to contributing to the multidisciplinary development teams by designing and executing pharmacokinetics data transfer between Exelixis and external vendors. ESSENTIAL DUTIES AND RESPONSIBILITIES: Assist in the planning, design and implementation PK data transfer plans from external vendors to Exelixis and from Exelixis to external vendors. Perform quality check of preclinical and clinical PK/TK data and reports and PK sections of regulatory documents (IND, IB, and NDA). Work with PK scientists and multiple functions to perform PK data cleaning and reconciliation for clinical studies. Support archiving of the final preclinical DMPK and clinical PK data and reports. Perform literature search to support PK data analysis. etc. | 9/8/2020 |
| 691 | Cayman Chemical Company Ann Arbor, MI Associate Scientist (Analytical Chemistry) MS in chemistry or related Exp: Not necessary for MS candidates |
We are currently seeking candidates for an Associate Scientist with the key duties and skills listed below: Duties and Responsibilities: Consistent compliance with and promotion of all Cayman values, policies, SOPs, and regulations including, but not limited to: Lab Notebook Policy. Safety and regulatory policies. Confidentiality policies. Timely, accurate data entry (AX, SharePoint, P-drive folders, Excel spreadsheets ). Perform assigned tasks with increasing independence: Operate and maintain HPLC, MS, GC, and optical rotation instrumentation. Perform analytical support services for internal chemists and external clients. | 9/1/2020 |
| 692 | Celerion Tempe, AZ Clinical Research Coordinator BA/BS Exp: 1-2 year(s) |
We have an exciting opportunity for Clinical Research Coordinator to join our Tempe, AZ clinical team! As a you work closely with our clinic operations team to ensure the success of our phase one clinical trials, Research Coordinators interpret study protocols to generate needed source documents, they add time and event codes into our systems to account for the needed tasks in a trial, they coordinate needed supplies for a given study and ensure we are ready to deliver. A background in clinical research or health care is a plus, but it is not required. We are seeking someone with well honed critical thinking skills, an ability to manage multiple projects at once, and well-developed time management skills. | 9/1/2020 |
| 693 | Celerion Tempe, AZ Entry-Level Project Coordinator (Clinical Research) BA/BS Exp: 1-2 year(s) |
We have an exciting opportunity for beginning project manager to join our Tempe, AZ clinical team! As a Clinical Project Coordinator you work closely with our clinic operations team to ensure the success of our phase one clinical trials. Project Managers interpret study protocols to generate needed source documents, they add time and event codes into our systems to account for the needed tasks in a trial, they coordinate needed supplies for a given study and ensure we are ready to deliver. A background in clinical research or health care is a plus, but it is not required. We are seeking someone with well honed critical thinking skills, an ability to manage multiple projects at once, and well-developed time management skills. | 9/1/2020 |
| 694 | Celerion Tempe, AZ Research Laboratory Assistant -- FT -- 6AM-2PM Shift AS/BS in a laboratory life science Exp: 1+ year(s) |
Research Laboratory Assistants handle human biological samples (primary blood and urine) and prepare them for routine testing and analysis. Additionally, they record raw data, transfer prepped samples to the onsite clinical laboratory, and barcode samples. This position is not involved in sample collection (i.e. phlebotomy). We are specifically seeking candidates with laboratory sample preparation and/or biological sample processing experience. This is a full time position scheduled for 40 hours per week with weekend availability expected. This position is slated to start on September 14, 2020. | 9/1/2020 |
| 695 | Celerion Tempe, AZ Fulltime Entry-level Lab Assistant BS in a laboratory science Exp: 1+ year(s) |
Research Lab Assistants handle human biological samples (primary blood and urine) and prepare them for routine testing and analysis. Additionally, they record raw data, transfer prepped samples to the onsite clinical laboratory, and barcode samples. This position is not involved in sample collection (i.e. phlebotomy). If you have recently graduated with a laboratory-based science degree (i.e. Biology, Microbiology, Chemistry) and are looking to begin fulltime work at a clinical site, we'd love to speak with you! | 9/1/2020 |
| 696 | Celerion Tempe, AZ Research Laboratory Assistant -- FT --2PM-10PM Shift AS/BS in a laboratory life science Exp: 1+ year(s) |
Research Laboratory Assistants handle human biological samples (primary blood and urine) and prepare them for routine testing and analysis. Additionally, they record raw data, transfer prepped samples to the onsite clinical laboratory, and barcode samples. This position is not involved in sample collection (i.e. phlebotomy). We are specifically seeking candidates with laboratory sample preparation and/or biological sample processing experience. This is a full time position scheduled for 40 hours per week with weekend availability expected. This position is slated to start on September 14, 2020. | 9/1/2020 |
| 697 | Celerion Tempe, AZ Research Laboratory Assistant -- FT --10PM-6AM Shift AS/BS in a laboratory life science Exp: 1+ year(s) |
Research Laboratory Assistants handle human biological samples (primary blood and urine) and prepare them for routine testing and analysis. Additionally, they record raw data, transfer prepped samples to the onsite clinical laboratory, and barcode samples. This position is not involved in sample collection (i.e. phlebotomy). We are specifically seeking candidates with laboratory sample preparation and/or biological sample processing experience. This is a full time position scheduled for 40 hours per week with weekend availability expected. This position is slated to start on September 14, 2020. | 9/1/2020 |
| 698 | Celerion Tempe, AZ Entry Level Clinical Data Assistant (FT) AS/AA/BS/BA Exp: 1-2 year(s) |
We seek an eager data entry master to join our data management team at our Tempe, AZ Phase 1 Research Clinic. This is a great entry-level opportunity to begin a career in clinical data management. This is a fulltime position, working 40 hours per week with shifts occurring onsite between 9AM-5PM, Monday-Friday. Essential Functions: Perform accurate data entry and verification for study specific External Studies, Celerion Standard, Spondor Provided EDC, and Sponsor Provided Paper CRFs (if applicable). Work with Clinical Data Manager for External Studies to create a working copy of the completed paper CRFs to ensure accurate and consistent data entry. Collate source data and signed disposition pages into final CRFs. | 9/1/2020 |
| 699 | Cell Signaling Technology Danvers, MA Research Associate - VSC BS in a biological science Exp: 1+ year(s) |
We are seeking a Research Associate to join our Validation Systems Core (VSC) team within our Product Development organization. The VSC serves as a centralized resource for innovation in the culture, treatment, lysis, and storage of cell lines. The Research Associate is responsible for providing well-characterized, high quality cells and lysates to the organization to support Product Development efforts focused primarily on affinity research reagents such as primary antibodies, in addition to other product types such as assay kits, conjugates, and ELISA pairs. This position is a dynamic role in a fun, fast paced environment. The VSC places emphasis on teamwork so candidates are expected to collaborate and work well with fellow group members. | 9/1/2020 |
| 700 | Cell Signaling Technology Beverly, MA Filling & Assembly Specialist I - 6-Month Contract HS diploma or equivalent Exp: 1+ year(s) |
The Filling & Assembly Specialist I functions as a member of our Global Supply Chain team to support the discrete manufacturing of our products. Specifically, the Packaging team is responsible for filling and assembly of final products to ensure finished goods inventory is ready and available for customers. This is a temporary 6-month assignment, with hours from 8 AM – 4 PM, Monday – Friday, 37.5 hours per week. Responsibilities: Precision aliquoting and filling of antibody products utilizing liquid handling techniques with strict adherence to SOPs to ensure product quality. Labeling of vials and preparation of packaging for component assembly, adhering to strict quality control guidelines to ensure labeling and packaging meets compliance requirements and standards. Inspecting and packaging product components with manual and/or automated systems to create final products for order fulfillment. Set-up, change-over and operation of labeling, pumping and packaging equipment. Data entry and updating to enable accurate inventory records. | 9/1/2020 |
| 701 | Cell Signaling Technology Danvers, MA Research Associate - Purification BS in cell biology, biochemistry, or chemistry Exp: 1-2 year(s) |
We are seeking a Research Associate to join our Purification team. S/he will assist with the purification of antibodies using Protein A and peptide affinity chromatography. The successful candidate should have basic knowledge of laboratory experience, good communication skills and be highly collaborative. Responsibilities: Benchtop purification as well as purifications performed robotically. Responsibilities for this position will also include inventory management, data entry and solution preparation. Researches and identifies opportunities for process and protocol improvements. Effectively follows SOPs and produces consistent results and throughput metrics. Stays current with scientific research and demonstrates a willingness to learn new skills and techniques. Mentor and guides others in scientific and technical matters. Can direct the efforts of others (e.g. summer interns) on small projects with assistance. | 9/1/2020 |
| 702 | Cellular Dynamics Madison, WI Laboratory Technician AS/AA in a relevant science discipline Exp: Not necessary for AS/AA candidates |
FUJIFILM Cellular Dynamics, Inc is recruiting for a laboratory technician to work in our cell manufacturing and research facility in Madison, WI. This role provides an outstanding opportunity for a dedicated and responsible individual to contribute to maintaining and improving the operations in our facility. Ideal candidates can demonstrate a track record of self-motivation, strong organizational skills, and dedication to their work. Essential Job Functions: Provide lab support for scientific personnel and overall operations. Place orders, maintain inventory, and stock laboratory supplies. Work with laboratory staff to maintain and mature organizational structure. Organize and put away daily shipments consistent with inventory management, housekeeping and safety standards. Perform maintenance on equipment as specified, including minor repairs and cleaning. | 9/1/2020 |
| 703 | Celsius Therapeutics Cambridge, MA Research Associate II, Immuno-Oncology, Target ID and Validation MS Exp: 1-3 year(s) |
We seek a passionate and committed bench scientist to join our team with a focus on oncology and immuno-oncology target validation. The successful candidate will have a sound understanding of cell biology and extensive experience with in vitro assay development. We’re looking for candidates excited by the opportunity to interrogate targets identified through single-cell genomics and functional genomics efforts. RESPONSIBILITIES: Develop in vitro assay systems involving primary mouse and human immune cells to execute on target validation plans. Evaluate mechanistic role of candidate targets using a variety of perturbation approaches, such as CRISPR, RNAi, and pharmacological tools. Flexibly deploy different analysis techniques to address experimental goals (e.g. FACS, qPCR, ELISA, ). | 9/1/2020 |
| 704 | Celsius Therapeutics Cambridge, MA Research Associate II, Autoimmune biology, Target ID and Validation MS Exp: 1-3 year(s) |
We seek a highly motivated bench scientist to focus on autoimmune target ID and validation. The successful candidate will have good prior experience in immune biology, with experience in assay development using immune cell types, including primary cell assays. Using this expertise, the successful candidate will gain experience learning how to apply large single cell and other datasets, as well as functional genomics approaches, towards the identification and validation of new targets. RESPONSIBILITIES: Develop and execute in vitro immune cell assays to functionally validate novel targets. Participate in the interrogation of single cell datasets towards the identification of novel autoimmune targets (prior experience with single cell RNA sequencing is not required). | 9/1/2020 |
| 705 | Centrillion Technologies Palo Alto, CA Mechanical Engineer - Instrumentation BS/MS in mechanical engineering Exp: 1-2 year(s) |
Centrillion is seeking a Mechanical Engineer to assist in the development of innovative genomic research instrumentation for performing various biochemical reactions and signal detection/analysis. Responsibilities: Work as part of a team driving products through their lifecycle including concept generation, prototyping, component and device assembly, extensive testing. Help generate creative solutions to design problems and demonstrate their feasibility by considering factors such as risk, reliability, manufacturability. Assist the Project Lead and other members of the Engineering Team in transitioning concepts into products using solid modeling tools, defining requirements, selecting materials and processes. Assist in request for quoting duties, interacting with suppliers and manufacturers, and documenting the development process. | 9/1/2020 |
| 706 | Centrillion Technologies Palo Alto, CA Laboratory Technician BA/BS in molecular biology, chemistry, genetics, or related Exp: 1-2 year(s) |
Centrillion is seeking Laboratory Technicians for their research and development teams. These positions are in a fast-paced, start-up environment, interacting with R&D scientists from a variety of backgrounds, with a heavy focus on molecular biology and biochemistry. Lab technicians will divide their time between hands-on laboratory work, data analysis, and lab organization and maintenance. The selected individuals will be working in a support role toward the development of new genomics technologies. The candidate will work with multiple scientists to assist with a broad range of duties including making buffers, following protocols, developing or adapting new protocols for new needs. | 9/1/2020 |
| 707 | Danaher Lodi, CA Manufacturing Engineering Technician II AA/AS Exp: 1-2 year(s) |
PRIMARY RESPONSIBLILITIES: Follows company specific Safety procedures/guidelines and Work Instructions. Support in the build, installations, setups and qualifying Robot, Robot End of Arm Tooling (EOAT), Sorting Station, Conveyors and manufacturing related equipment as assigned. Support in any design improvements and changes to Injection Molding system in manufacturing. Support in develop and maintain documentation, initiate and implement assigned change orders. Complete assigned tasks and provide information that supports qualification, such as design, documentation, implementation and validation execution of new/changed equipment or process. Ability to learn to utilize/interpret precision measurements tools. | 9/1/2020 |
| 708 | Danaher Sunnyvale, CA Regulatory Affairs Specialist II MS in a life science or related Exp: 0-2 years |
ESSENTIAL JOB RESPONSIBILITIES: Responsible for regulatory project timelines and management of global regulatory submissions. Coordinate and prepare regulatory submissions to ensure compliance with international regulations and guidelines. Establish and review Regulatory Affairs priorities as they relate to department and company goals and objectives. Interact with global regulatory leaders and peers to expedite approval of pending registrations. Support internal and external departments to generate protocols and reports for registration purposes. Maintain a "focused urgency" as required by specific events. Recognize potential problems by actively reviewing and analyzing internal and external factors. Assess potential impact and/or applicability to other related areas. | 9/1/2020 |
| 709 | Danaher Lodi, CA Injection Molding Technician AA/AS Exp: 1-2 year(s) |
The position will work with all phases of the Injection Molding on production floor, (Prefer Nessie and Yushin experience) from start- up of molds, troubleshooting, set up of molds, and assist in monitoring quality. Responsible for setting and adjusting machine controls according to established window parameters while troubleshooting “Quality Issues” during production runs. Help Identified and diagnose technical issues for a quick resolution and immediate response to avoid press down time. Ensure to follow SOP and WI procedure and log in all data require for process on each lot running; as well as following all safety precautions to perform all tasks on a safe environment. | 9/1/2020 |
| 710 | Ceva Verona, WI Maintenance Technician II - Verona AA/AS Exp: 1 year |
The Maintenance Technician II is responsible for assisting the Facilities and Engineering Manager with the maintenance, quality, and upkeep of the manufacturing, testing, and animal holding facilities, and the equipment and utilities at each location, in support of the manufacture of biological products consistent with the corporate objectives and external, international, and federal regulatory requirements. Responsibilities and Key Duties: Perform preventive maintenance on HVAC, electrical, structural and other non-critical equipment. Assist in the execution of PMs on critical equipment. Perform non-scheduled maintenance, on all non-critical equipment, in a timely manner as requested via the MWO system. Review and document all repairs, alarms and PM activities according to applicable Standard Operating Procedures. | 9/1/2020 |
| 711 | Charles River South San Francisco, CA Research Associate BS in neuroscience, pharmacology, biology, or related Exp: 1+ year(s) |
We are seeking an experienced Research Associate (biotechnical) for our Discovery site located in South San Francisco, CA. ESSENTIAL DUTIES AND RESPONSIBILITIES: Rodent surgeries. Microdialysis and the development and running of rodent behavioral tests in support of CRO activities. Involvement in the design of experimental protocols and procedures, running experiments, and analyzing data. | 9/1/2020 |
| 712 | Charles River Wilmington, MA Technologist - IVB AA/AS in a biological science or related Exp: 1 year |
Job Summary: The following are responsibilities related to the Technologist - IVB in Wilmington, MA: Perform daily test article/substance administration, observation and recording of physical signs of species for contracted laboratory studies. Prepare cage tags and individual animal number tags; prepare and autoclave cages. Prepare data forms for routine study procedures. Assist with preparation of data forms for specialized study procedures. Record study parameters as required by protocol. Ensure adequate supply of dosage equipment during the course of study. Assist in ensuring adequate supply of additional study specified materials such as blood collection tubes. Assist in preparation of test agents. | 9/1/2020 |
| 713 | Charles River Mattawan, MI Animal Research Technician - Animal Services BS/MS Exp: None necessary |
We are seeking an Animal Research Technician for our Animal Services Team located in Mattawan, MI. An Animal Research Technician is responsible for: performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality, administering substances to animals; 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. The following are minimum requirements related to the Animal Research Technician position. | 9/1/2020 |
| 714 | Charles River Malvern, PA Technician 1 Microbiology BS in biology or related Exp: 1+ year(s) |
We are seeking a Technician 1 Microbiology for our Biologics Testing Solutions site located in Malvern, PA. The responsibilities of this role will be specific to the Sterile Services division of the Microbiology department. The following are the responsibilities of the Technician 1 Microbiology: Performance of direct inoculation and membrane filtration sterility testing. Performance of direct inoculation and membrane filtration bacteriostasis and fungistasis testing. Growth promotion testing of sterility and other microbiological testing media. | 9/1/2020 |
| 715 | Charles River Wayne, PA Technician 1 Virology BA/BS in biology or related Exp: 0-1 year(s) |
Under direct supervision, the laboratory technician will be responsible for performing basic daily laboratory tasks as they relate to the operations performed within the Virology Department. The following are responsibilities related to the Technician 1 Virology: Perform routine laboratory tasks related to Virology testing. Practice proper aseptic and sterile processes during cell culture. Perform calibration, monitoring and cleaning of laboratory and lab equipment. Maintain inventory of necessary supplies by ordering and / or preparing reagents, media and solutions. | 9/1/2020 |
| 716 | Charles River Durham, NC Electron Microscopy Technician 1 AS/BS in biology or related Exp: 0-1 year(s) |
Perform basic Electron Microscopy sample preparation with minimal supervision. Participate in the documentation of all activities as required. May also assist with setting up study files, inventories, and sending reports and study materials. We are seeking an Electron Microscopy Technician I for our Safety Assessment site located Durham, NC. The following are responsibilities related to the Electron Microscopy Technician I: Log in samples and set up study files for each protocol. Trim tissue, process/embed both viral and tissue specimens with supervision. Prepare solutions/reagents, cut thick/thin sections on the ultramicrotome, and stain slides/grids. Copy and send reports, prepare delivery slips, and return materials to the client. Understand and conduct all processes in compliance with Good Laboratory Practice (GLP) regulations, corporate Standard Operating Procedures (SOP), and the protocol. | 9/1/2020 |
| 717 | Charles River Charleston, SC Quality Control Associate BA/BS Exp: 1 year |
We are seeking a Quality Control Associate for our Microbial Solutions site in Charleston, SC. This role will, ensure the quality and integrity of product by testing incoming materials, excipients and final product. The Quality Control Associate will be responsible for the following: Ensuring the quality and integrity of product by testing PTS cartridges, Limulus Amebocyte Lysate (LAL), incoming materials, and excipients. Perform Crude Lysate recovery procedures during the Horseshoe Crab Bleeding Season (Summer Months). Long-Term Stability monitoring of samples. Using technical writing to perform investigations and complete exception records. Attention to detail in all aspects of work is essential. | 9/1/2020 |
| 718 | ChemGenes Wilmington, MA Junior Chemist BS in chemistry Exp: Not necessary for BS candidates |
The job duties: Manufacture of DNA & RNA compounds. Assist Senior Chemists. Prepare test solutions, reagents and ability to carry out reactions, to produce specialized ultra pure DNA/RNA synthesis products. Operate rotary evaporators, chillers, Preform column chromatography: small scale (on the bench) & large scale. Follow SOPs of standard products; report any deviations to Senior Chemists. Communicate with QC & QA department to update/create certificates of analysis. Maintain timely documentation of work. Evaluate data & prepare technical reports. General lab maintenance as necessary. | 9/1/2020 |
| 719 | CheminPharma Woodbridge, CT Associate Scientist, Medicinal/Synthetic chemistry BS/MS in synthetic chemistry Exp: 0-5 years |
The successful candidate will be an experienced chemist with state of the art knowledge of synthetic organic chemistry and will be a motivated, creative, hands-on laboratory scientist with the ability to interact effectively with team members and external customers. Major responsibilities will involve design, synthesis, purification, and characterization of novel chemical entities and the management of general chemistry lab operations under the direction of senior scientific staff. The qualified individual is expected to contribute to process development and scale-up of key intermediates. | 9/1/2020 |
| 720 | ChemPacific Baltimore, MD Chemist MS 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. | 9/1/2020 |
| 721 | ChemPacific Baltimore, MD Budget Analyst MS in finance Exp: Not necessary for MS candidates |
Duties: Work under the Chief Financial Officer to coordinate accounting and financial operations of the company to project and plan future earnings and expenditures. Apply principles of business finance to analyze financial records and financial operations in order to determine accuracy of financial records, efficiency of operations and effectiveness of budget control and to estimate future revenues and expenditures. Provide strategic analysis and advice to senior management for strategic decision making for entering into joint venture projects with businesses both in China and the United States to set up new production facilities in China, and new warehousing facilities and wholesale outlets in the United States; and Prepare budget reports, as well as long term budget plans with cost analysis and fiscal allocation, and maintain budgeting systems with the company to provide control of expenditures for product development and new business acquisitions and ventures. | 9/1/2020 |
| 722 | Clinlogix Lower Gwynedd, PA Clinical Project Assistant I AS/BS in business administration, a life science, or related Exp: 1 year |
The Clinical Project Assistant I role is an entry level position to the clinical research industry. This role requires organizational skills with a high attention for detail. The ability to work in a team environment, meet deadlines, and prioritize and balance work from multiple projects is necessary. Excellent verbal and written communication skills are essential. This position will support the Clinical Project Assistants II/Senior Clinical Project Assistants, Clinical Project Managers, Clinical Research Associates and other Study Team Members as a supporting role for ongoing clinical studies. The Clinical Project Assistant I position is an integral member of the clinical project team providing support and troubleshooting on various aspects of project. | 9/1/2020 |
| 723 | Coda Therapeutics South San Francisco, CA Research Associate/Sr. Research Associate Ion Channel Assay Development BS/MS in cell biology Exp: 1-2 year(s) |
This position will manage a wide range of administrative and executive support related tasks and will be able to work independently with little or no supervision. Primary Responsibilities: Assay Development: Design and validate cell-based fluorescence and automated electrophysiology assays to support receptor lead selection. Compound Screening: Execute medium throughout compound screening and follow-up pharmacological evaluation of small molecules on lead chemogenetic receptors. Organization and Communication of Data: Analyze and communicate data in written and oral modalities in both informal and formal settings. Generate and manage meticulous method protocols, data, and analysis reports in a clear and highly organized fashion. | 9/1/2020 |
| 724 | Codexis Redwood City, CA Research Assistant/Associate, Biotherapeutics Lead Discovery BS/MS in biochemistry, structural biology, bioengineering, or related Exp: 0-6 years |
Codexis seeks a highly motivated researcher to join the Biotherapeutics Lead Discovery group to support our efforts to engineer novel biotherapeutic proteins. We are looking for a scientific researcher proficient in protein biochemistry and analytical methods development. Successful candidates will be part of an interdisciplinary, dynamic and enthusiastic biotherapeutics discovery team responsible for implementing Codexis’ core technologies and delivering candidate biologics. Responsibilities include: In collaboration with cross-functional project team members, perform high-throughput (HTP) screening campaigns to support directed evolution of next-generation biotherapeutics. Express recombinant protein variants in E. coli or mammalian cells for in vitro profiling. Execute and troubleshoot assay protocols for protein characterization (e.g., biochemical, enzyme activity, and cell-based assays). Adapt assays for HTP screening. | 9/1/2020 |
| 725 | Codiak Lexington, MA Manufacturing Associate, Internal Drug Product Manufacturing AS/BS in biology, chemistry, mechanical engineering, or related Exp: 1-3 year(s) |
The Manufacturing Associate, Internal Drug Product Manufacturing is a production position focused on the activities associated with a closed-RABS isolator drug product filling operation. The position will be heavily manufacturing floor-based during preparation and execution of drug product filling, inspection and labeling activities. This position will report to the Supervisor of Internal Drug Product Manufacturing and is expected to interact with Quality Assurance and Control, Facilities Operations and Materials Management groups. The position is based in Codiak’s new clinical manufacturing facility “CMF” in Lexington, MA. | 9/1/2020 |
| 726 | Cognate Bioservices Memphis, TN QC Analyst I - BioAssay BS in a biological science Exp: 0-3 years |
ESSENTIAL DUTIES AND QUALIFICATIONS: Adheres to Standard Operating Procedures (SOPs) and good documentation practices to ensure data integrity and traceability. Perform cell based immunological in vitro methods (e.g., cytotoxicity, HLA-restriction, cell proliferation, ). Perform release testing utilizing a variety of techniques ranging from compendia assays like pH and osmolality to more complex assays like, but not limited to, proliferation and cytotoxicity. Be able to quickly learn various methods and participate in the troubleshooting of assays. Enters observations and results into the appropriate trending databases for periodic analysis and trending. | 9/1/2020 |
| 727 | Compass Therapeutics Cambridge, MA Entry Research Associate - Immunology and IO BS/MS in immunology, molecular biology, biochemistry, or related Exp: 1-3 year(s) |
We are a clinical stage Biotech company located in Cambridge that has been steadily growing. We are looking for a self-driven Senior or Junior Research Associate to play a critical role in supporting the research and development of the Immunology Program. This position will assume a key role in developing and implementing novel immunological assays in support of our proprietary therapeutics through an innovative antibody engineering platform. The position will be developing immunological assays in both cell lines and primary cells for identification and prioritization of therapeutic targets for clinical development. | 9/1/2020 |
| 728 | Compass Therapeutics Cambridge, MA Research Associate, Immunology BS/MS in immunology, molecular biology, biochemistry, or related Exp: 1-5 year(s) |
Our Immunology team is seeking a hands-on scientist at our Cambridge, MA site. This role will play a critical role in supporting the research and development of the Immunology Program. This position will assume a key role in developing and implementing novel immunological assays in support of our proprietary therapeutics through an innovative antibody engineering platform. The position will be developing immunological assays in both cell lines and primary cells for identification and prioritization of therapeutic targets for clinical development. The ideal candidate will have a proven track-record of developing creative and novel immunology-based assays for solving complex biological problems, as well as a broad understanding of therapeutic drug discovery and its applications, | 9/1/2020 |
| 729 | Compass Therapeutics Cambridge, MA Research Associate, In Vivo Immunopharmacology BS/MS in immunology, cell biology, or related Exp: 1+ year(s) |
Our in vivo Immunopharmacology team is seeking a hands-on scientist at our Cambridge, MA site. This individual will perform animal studies and in vitro assays to evaluate the anti-tumor activity of novel protein biologics and drive their advancement into the clinic. Experience with immunological assays and in vivo work experience are required. Candidates with work experience using immuno-oncology mouse models are encouraged to apply. Practical knowledge of ex-vivo primary cell manipulations, tissue culture and immunoassays highly preferred. The Research Associate Scientist position is an entry-level position that leverages existing knowledge and technical expertise to conduct preclinical studies under supervision. | 9/1/2020 |
| 730 | ConforMIS Wilmington, MA Manufacturing Engineer I BS/MS in engineering Exp: 1-3 year(s) |
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. Essential Duties and Responsibilities: Develop and maintain strong, internal working relationships across ConforMIS. Understand the objectives, responsibilities, and mission of the Operations department and works towards those goals. Prioritize and plan work activities; adapt for changing conditions. Initiation, execution, and documentation of IQ, OQ, & PQ activities. Optimization of manufacturing processes (5S) for Lean Manufacturing. | 9/1/2020 |
| 731 | Bristol Myers Squibb New Brunswick, NJ Associate Scientist GQAST Pharma & Forensics BS/BA Exp: 1-3 year(s) |
The Associate Scientist will be involved in hands on laboratory testing of foreign matter samples associated with manufacturing investigations, product quality complaint samples, and suspect product samples using spectroscopic techniques (NIR, Raman and mid-IR), microscopy, and wet chemistry methods. This work will cover the entirety of the BMS commercial portfolio, including both biologics and small molecule assets. They will provide analytical support to Global Quality, Corporate Security, External Manufacturing, and Manufacturing Operations, and to both internal and external sites as required. Duties: Support manufacturing investigations through characterization and identification of extraneous/foreign matter samples using relevant analytical techniques (mid-IR, Raman, SEM/EDS, microscopy). | 8/26/2020 |
| 732 | Bristol Myers Squibb Seattle, WA Senior Research Associate, Cell Therapy Process Technologies MS in biology, chemical engineering, or related Exp: 1+ year(s) |
DUTIES AND RESPONSIBILITIES: Develop automated scale down model platform for cell therapy process development. Develop automated unit operations for adoptive T-cell therapy manufacturing. Evaluation of cell therapy manufacturing prototype devices. Design and execute small and large-scale cell therapy process development experiments. Analyze data from flow cytometry, cell functionality, or chemical assays. Write technical documents including development reports, batch records, and Standard Operating Procedures. Train operators or other engineers and scientists. | 8/26/2020 |
| 733 | Bristol Myers Squibb Manati, PR Microbiology Analyst BS in biology, biotechnology, medical technology, or microbiology Exp: 1 year |
Performs laboratory analysis or tasks following established procedures and in full compliance with current governmental regulations, official compendia and any other policy / regulation to generate reliable and timely results, to comply with releases due date, reducing cycle time, and providing internal / external customer satisfaction. Responsibilities: The analysis are: bacterial endotoxin, sterility test, bioburden / microbial limit, growth promotion, particulate matter to parenteral products, microbial identification, pH test , ,osmolality, ,density, protein concentration and other analysis related to the release of the products being manufactured. In addition do microbial analyses of: manufacturing utilities (i.e. water, clean condensate, compress air, nitrogen, ). | 8/26/2020 |
| 734 | Bristol Myers Squibb Devens, MA Associate / Assistant Scientist BS/MS in chemical engineering, bioengineering, biology or chemistry Exp: 0-6 years |
The Associate/Assistant Scientist within the Biologics Development - Upstream group will participate in the development and optimization of upstream processes for production of biologics at different clinical stages. The successful candidate will participate in the execution of bench-scale experiments using high-throughput, shake flask, or bioreactor cell culture systems to improve cell culture processes. Under general direction, the position requires participation in the design and execution of experiments, interfacing mainly with other upstream and occasionally with downstream and analytical personnel to achieve process development objectives. A successful candidate will work effectively in a cross-functional process development team and also be able to work independently to accomplish overall project goals. | 8/26/2020 |
| 735 | Bristol Myers Squibb New Brunswick, NJ Associate Scientist MS in biotechnology, immunology, cell biology, molecular biology or related Exp: Not necessary for MS candidates |
Responsible for assay development, validation and Good Manufacturing Practice (GMP) testing for early and late stage biopharmaceutical drug development programs by utilizing knowledge of GxP (Good x = Manufacturing/ Laboratory /Clinical Practices) and specialized equipment such as optical density plate readers, luminometers, cell counters, time-resolved fluorescence plate readers, imaging microscopy, and fluorescence-activated cell sorting, and experience with laboratory technique such as ELISA, mammalian cell culture, bioassay applications, and cell signaling pathways. Carry out assigned laboratory work and other functional duties. Maintain research and GxP notebooks documenting all laboratory work consistently and accurately. | 8/26/2020 |
| 736 | Brooks South Plainfield, NJ Part-time Night Shift Laboratory Technician HS diploma/AS Exp: 1+ year(s) |
Our Lab Techs are: Quality driven processers. When our customers send us samples for sequencing, they help to prepare and process these samples as quickly and as awesomely as possible, while maintaining the highest quality standards in the industry. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. etc. | 8/25/2020 |
| 737 | Brooks South Plainfield, NJ Associate Bioinformatics Scientist BS/MS in bioinformatics Exp: 0-3 years |
Responsibilities: Perform data analysis and generate reports for customer projects. Develop novel algorithms and build customized pipelines for clinical service projects. Build LIMS workflows for operation service lines. Evaluate and identify optimal NGS data analysis solutions. Conduct literature search for various genomics research areas etc. | 8/25/2020 |
| 738 | Brooks South Plainfield, NJ Lab Assistant HS diploma Exp: 1+ year(s) |
We are seeking a Lab Assistant to join our Next Generation Sequencing team. Responsibilities: Check inventory and replenish consumable sequencing supplies. Assist in sample sorting and properly distribute them. Maintain laboratory cleanliness. Document and track daily work flow. Help with logistics as needed. Prepare supplies and assist Associate Scientists. etc. | 8/25/2020 |
| 739 | Brooks South Plainfield, NJ Associate Scientist I BS in a biological science Exp: 1+ year(s) |
The Associate Scientist position in our Next Generation Sequencing department is a great entry-level role with room for growth and advancement. If you have the desire to work in a casual yet results-driven environment that embraces innovation- then you’re just what we’re looking for! Responsibilities: Prepare amplified template libraries for high-throughput sequencing. Carry out DNA sequencing on next-generation DNA analyzers. Perform routine maintenance of DNA analyzers and related equipment. etc. | 8/25/2020 |
| 740 | Essity South Glens Falls, NY RST Process Engineer Converting BS in paper science, chemical, mechanical, electrical or industrial engineering Exp: 1+ year(s) |
This role serves as the day-to-day owner of the machine processes and process control systems for the plant. Owns and manages the development of troubleshooting skills of the manufacturing professionals. Acts as a subject matter expert for the machine processes. Participates and/or leads in Continuous Improvement projects. Helps to identify and support projects that will improve productivity, waste, quality and safety performance on a long term basis. We’re looking for people who embody our values, aren’t afraid to challenge, innovate, experiment, and move at a fast pace. We’re always looking for ways to improve our products and ourselves. If this is you, we’d love to talk. etc. | 8/25/2020 |
| 741 | BD Mannford, OK Assembler 2, General HS diploma or equivalent Exp: 1-3 year(s) |
Job Description: Commitment to Safety, by following site safety procedures and utilizing safety equipment as required for daily tasks. Uses batch record instructions, job aids, standard operating procedures, and product specifications to execute production activities. Maintains accurate documentation, records and logs in accordance with FDA (Food and Drug Administration), GMPs (Good Manufacturing Practices) and ISO9000 (International Organization for Standardization). Ability to perform minor troubleshooting and problem solving in areas of set-up of equipment and processes. Ability to perform rework and re-packaging of materials as needed. Ability to work in teams to achieve operational goals while being engaged in the process. Communicating issues and concerns to lead or designee. Performs assembly by following released procedures. etc. | 8/25/2020 |
| 742 | BD Columbus, OH Manufacturing Team Manager, Night Shift BS/BA Exp: Not required for BS/BA candidate |
Under the direct supervision of the Unit Manger and Product Line Leaders. Directs and manages shift activities for assigned operations to ensure compliance to cost, quality, safety, human resource and regulatory plans and requirements. Establish and implement programs designed to assure control of processes and products that meet or exceed established standards and specifications. Informs management of quality problems and solutions relative to FDA and ISO compliance. RESPONSIBILITIES: Manages shift activities to achieve an overall objective of continuous improvement in productivity, quality, cost, budget compliance and attainment of strategic objectives. As required monitor and coordinate all plant shift operations - - timely communicate issues to unit manager. etc. | 8/25/2020 |
| 743 | BD Baltimore, MD Machine Operator 2 AS/AA Exp: 0 years |
Performs routine set up, operation, minor routine maintenance, preventative maintenance (PM) and troubleshooting of moderately complex/automated manufacturing equipment. Controls and adjusts machine settings. Inspects in-process parts to ensure consistent quality and removes defective product, packaging, and component material. Assists with root-cause analysis activities for process or product exceptions. Checks work using prescribed gauges, jigs and fixtures to measure close tolerances. May monitor quality in accordance with statistical process or other control procedures. Ensures accurate documentation of all relevant quality, safety, and maintenance documents. Identifies, troubleshoots, and resolves basic issues associated with the machine performance and/or product quality. etc. | 8/25/2020 |
| 744 | BD Glens Falls, NY Manufacturing Team Member I Crosser 1st Shift HS diploma or equivalent Exp: Not required |
Performs any combination of tasks involved in the manufacture and assembly of medical devices. Job Description: Responsible for following safety policies and procedures. Responsible for following all required GMP’s and applicable manufacturing procedures. Perform a variety of duties to assemble all types and sizes of product, components, and sub-assemblies using a variety of standard and specialty assembly machines or hand operations. May be required to press, bond, solder, flare, strip, clamp, sand, weld, mount/takedown or inspect for appearance, gauging of parts by “no-go” or “go” gauges and set fixtures. etc. | 8/25/2020 |
| 745 | BD Baltimore, MD Quality Engineer II (Operations) MS in engineering, a biological science, chemistry, or computer science Exp: 1 year |
DUTIES: Maintain International Organization for Standardization (ISO) and regional regulatory requirements. Key elements focus on multiple aspects of quality for product design, manufacturing (assembly and test), inspections and customer complaints throughout the product life cycle. Develop Device History Files and maintain in a manner consistent with regulatory requirements. Generate process/product quality information in the form of CTQ (Critical to Quality) indices, recommendations and solutions to emerging issues, to share with project team/operations/suppliers. Supports the coordinated integration of new products into Manufacturing / Operations. Ensures BD Diagnostic Systems divisional, departmental policies, procedures, practices and facilities are in compliance with all applicable regulatory policies. Understanding and coaching others on Quality Systems and procedures. etc. | 8/25/2020 |
| 746 | BD El Paso, TX Quality Assurance Technician I AS/AA in quality, life sciences, or engineering Exp: 1 year for AS/AA candidates |
This position is critical to the accurate evaluation of incoming materials, component, subassembly and finished product quality. Responsibilities include inspection, analysis of results, determining final disposition of some product and detecting nonconforming conditions. The Quality Assurance Tech I is also responsible for working within an established framework of compliance and developing and/or implementing improvements to product quality and the quality system. Principal Accountabilities: Inspect incoming and in-process materials, for compliance with established quality specifications. Work with production, receiving, and materials personnel to accurately complete required testing and documentation, determine correct disposition, and apply correct status labeling. Update material disposition status in SAP. etc. | 8/25/2020 |
| 747 | BD Sandy, UT Molding Machine Operator HS diploma or equivalent Exp: 1-2 year(s) |
Molding operator/technician is responsible for molding production in assigned area and minor maintenance activities on assigned presses. Job Responsibilities: Operate injection molding presses to supply downstream equipment with molded components including inspection of components and requesting technical support to maintain part quality. Conduct minor maintenance activities on assigned presses. Work with other molding team members to keep equipment running during breaks and call-outs. Operate multi cavity injection molding machines and auxiliary equipment to manufacture product which conforms to quality specifications, at the rated output. etc. | 8/25/2020 |
| 748 | Cabaletta Bio Philadelphia, PA Cellular Immunology Senior Research Associate/Associate Scientist MS in biology Exp: Not necessary for MS candidates |
Reporting to a Senior Scientist, Cellular Immunology, we are seeking an experienced, motivated, and highly skilled Cell Biology Associate Scientist. Under scientific and technical supervision, the candidate will perform various cell-based assays and maintain cell lines to contribute to the discovery and development of novel therapeutics at Cabaletta. The position offers growth into additional areas such as translational research and molecular biology, immunology and cell therapy. The position involves both technical and operational responsibilities. etc. | 8/25/2020 |
| 749 | Cabaletta Bio Philadelphia, PA Molecular Biology Senior Research Associate/Associate Scientist MS in biology Exp: Not necessary for MS candidates |
Reporting to the Senior Scientist, Protein Production and Molecular Cloning group, we are seeking an experienced and motivated Molecular Biology Associate. Under scientific and technical supervision, the candidate will design and produce molecular constructs to be utilized for vector development and protein production. The candidate will also engage in characterizing peptides and proteins, perform ELISAs (Luminex™), and other assays as needed. 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. etc. | 8/25/2020 |
| 750 | Cambrex Longmont, CO Formulations Scientist BS Exp: 0-3 years |
We are seeking an Associate Scientist to support formulation design and development activities within the Formulation team. This role will be responsible for executing oral solid dosage formulation experiments for drug product process development and analytical testing to primarily support early stages of the CDMO projects. Responsibilities: Assists on formulation and drug product process development projects, with an emphasis on early stages of development. Conducts physicochemical characterization and pre-formulation activities. etc. | 8/25/2020 |
| 751 | Cardiovascular Systems Pearland, TX Assembly Technician HS diploma or equivalent Exp: 1 year |
The Assembly Technician I will be expected to perform basic functions to complete day-to-day production activity. The position requires a highly motivated, positive individual that can work both independently and in a “team” environment. Assembly Technician I level employees will be expected to perform all job duties in the areas they are assigned under basic supervision. They will stay on task and complete quality work with accurate documentation. He/she will be a valuable and trustworthy asset to their work area through quality work of trained processes. This individual must be dedicated to the success of CSI and its quest to continually improve its operations, as well as perform duties to manufacture CSI products, meeting FDA, OSHA, GMP/MDD and ISO compliance requirements. etc. | 8/25/2020 |
| 752 | Cardiovascular Systems ST. Paul, MN Assembly Technician HS diploma or equivalent Exp: 1 year |
The Assembly Technician I will be expected to perform basic functions to complete day-to-day production activity. The position requires a highly motivated, positive individual that can work both independently and in a “team” environment. Assembly Technician I level employees will be expected to perform all job duties in the areas they are assigned under basic supervision. They will stay on task and complete quality work with accurate documentation. He/she will be a valuable and trustworthy asset to their work area through quality work of trained processes. This individual must be dedicated to the success of CSI and its quest to continually improve its operations, as well as perform duties to manufacture CSI products, meeting FDA, OSHA, GMP/MDD and ISO compliance requirements. etc. | 8/25/2020 |
| 753 | Zoll Remote, IL Field Technician AS/AA Exp: Not necessary for AS/AA |
Responsible for providing onsite product support to specific customer accounts typically by contract. Product support consists of logistics, deployments, on-site trouble-shooting of product, preventative maintenance (PM) and software upgrades. Essential Responsibilities: Product support on-site and via telephone. Assist customer with application of equipment. Escalates customer related issues to Service Manager and CQA Regional Manager. Performs trouble-shooting on-site and corresponds with ZOLL Tech support staff to document the details related to the service and support activity. Performs on-site PM’s for service agreement devices / accounts. Potential for deployments or PM’s to other customers in region at the direction of the Manager. Able to maintain customer specific information related to service activity. etc. | 8/26/2020 |
| 754 | Zoll Cheswick, PA Assembler I HS diploma or equivalent Exp: 0-3 years |
The Assembler I’s primary function will be to perform light mechanical assembly and electronic assembly tasks as assigned. This includes the repair, assembly or disassembly of various devices. Essential Duties and Responsibilities: Works under direct supervision. Applies basic skills in procedures, techniques, tools, materials and equipment. Performs routine assembly, modification and repair of electronic and electrical assemblies. Working from noncomplex wiring and assembly drawings, operation sheets, engineering specifications, sketches and running sheets, performs initial and basic wiring and assembly operations to complete prototype and production units. Completes wiring connections from one terminal point to another and solders each terminal, working to close tolerances. Uses judgment in reworking or rewiring any unit to bring it within quality control specifications. etc. | 8/26/2020 |
| 755 | Zoll Cheswick, PA Material Handler I HS diploma or equivalent Exp: 0-1 year(s) |
Performs manual and clerical duties related to shipping, receiving, inspecting, storing, issuing and delivering a variety of materials, equipment and supplies. Essential Duties and Responsibilities: Customer oriented. Perform Cycle Count daily. Process incoming Purchase Order receipts. Issue components to all types of work orders. Fill stock requests. Enter WIP receipts. Perform T-Transaction for quick turn items. Perform work order traceability. Locate raw material in bin location. Perform daily shipping activities. etc. | 8/26/2020 |
| 756 | Zoll Pawtucket, RI QA Engineer BS/BA Exp: 1-3 year(s) |
The primary purpose of the position will be ensuring that complaints are properly investigated and documented as well as verifying that outgoing units comply with stated guidelines. In addition, the position supports the resolution of customer issues in order to determine the cause of the problem and to initiate the appropriate corrective action. In some cases, formal reports to customer will be required to explain the problem and what was done to correct it. Moreover, the Quality Assurance Engineer will be required to conduct analysis and trending of information and perform inspections on incoming finished goods. etc. | 8/26/2020 |
| 757 | Zoll Chelmsford, MA Quality Assurance Engineer BS/BA Exp: 1-3 year(s) |
The primary purpose of the position will be ensuring that complaints are properly investigated and documented as well as verifying that outgoing units comply with stated guidelines. In addition, the position supports the resolution of customer issues in order to determine the cause of the problem and to initiate the appropriate corrective action. In some cases, formal reports to customer will be required to explain the problem and what was done to correct it. Moreover, the Quality Assurance Engineer will be required to conduct analysis and trending of information and perform inspections on incoming finished goods. etc. | 8/26/2020 |
| 758 | Zoll East Providence, RI R&D Technician II AS/AA Exp: 0 years |
Perform R&D lab technician duties that include testing equipment, building prototype assemblies, building test equipment, and performing associated administrative duties such as lab cleanup and maintenance. Requires only moderate oversight in completing tasks. Essential Functions: Builds R&D test fixtures per specifications provided, providing design assistance and feedback. With minimal supervision, executes test protocols to completion, which includes coordinating the manufacturing and testing of the samples, reviewing the test procedures and data for accuracy and completeness, summarizing and analyzing the data or reviewing summaries for completeness, and informing the appropriate project leader of any questions or unexpected results that arise during testing. etc. | 8/26/2020 |
| 759 | Solique Warsaw, IN Field Service Technician I AS/BS in electronics or industrial mechanics Exp: Not necessary for AS/BS candidates |
We are seeking a Field Service Technician to learn, develop and execute the basic necessary skills required to perform the job of a ZEISS Service Technician. Service Technicians install, troubleshoot and repair ZEISS Industrial Quality Solutions equipment onsite at our Customers Locations. We are looking for people who are keen to try something new: Demonstrate customer service skills and knowledge with a high level of passion and dedication. Demonstrate strong and efficient ability to learn a skill on entry class Coordinate Measuring Machines utilizing mechanical and electronic aptitude. etc. | 8/26/2020 |
| 760 | Solique St. Cloud, MN Optical Lab Operator (Freeform, 1st Shift) HS diploma or equivalent Exp: 0-2 years |
Performs routine production duties associated with various aspects of lens production paying close attention to quality, quantity and efficiency. This position focuses on our Freeform Surfacing area washing lenses, inspecting and taping lenses, matching tools, polishing, running generators, inspecting and coating (backside). Qualifies and inspects product to ensure compliance with CZV specifications and standards. Complies with all safety regulations as well as maintains a clean and safe work environment. etc. | 8/26/2020 |
| 761 | Solique St. Cloud, MN Optical Lab Operator (Distribution, 3rd Shift | 20% Shift Differential) HS diploma or equivalent Exp: 0-2 years |
Performs routine production duties associated with various aspects of lens production paying close attention to quality, quantity and efficiency. This position focuses on our Freeform Surfacing area washing lenses, inspecting and taping lenses, matching tools, polishing, running generators, inspecting and coating (backside). Qualifies and inspects product to ensure compliance with CZV specifications and standards. Complies with all safety regulations as well as maintains a clean and safe work environment. etc. | 8/26/2020 |
| 762 | Solique St. Cloud, MN Optical Lab Operator (Presurfacing, 3rd Shift | 20% Shift Differential) HS diploma or equivalent Exp: 0-2 years |
Performs routine production duties associated with various aspects of lens production paying close attention to quality, quantity and efficiency. This position focuses on our Presurfacing area pulling lenses, training orders, tracing frames and pairing frames with orders. Qualifies and inspects product to ensure compliance with CZV specifications and standards. Complies with all safety regulations as well as maintains a clean and safe work environment. etc. | 8/26/2020 |
| 763 | Solique Minneapolis, MN Field Service Technician I AS/BS in electronics or industrial mechanics Exp: Not necessary for AS/BS candidates |
Demonstrate customer service skills and knowledge with a high level of passion and dedication. Demonstrate strong and efficient ability to learn a skill on entry class Coordinate Measuring Machines utilizing mechanical and electronic aptitude. Perform necessary administrative paperwork in complete and accurate manner. Solutions oriented with ability to work independently in a high pressure, fast paced and innovative environment. Travel requirement is 80-100% including international as needed. etc. | 8/26/2020 |
| 764 | CRISPR Therapeutics Cambridge, MA Research Associate (Toxicology) BA/BS Exp: 0-2 years |
CRISPR Therapeutics is seeking a motivated individual to join our in vivo pharmacology team. The candidate will be responsible for implementation of in vivo studies involving mice and rats and should be comfortable handling and administering test articles to both species. The team interacts with most of the research groups within CRISPR, offering the candidate exposure to a variety of different programs and platforms. The candidate will work with team members on all aspects of the in vivo study: design, administration, in-life observations, post mortem analysis, report generation, and data presentation. Familiarity with downstream analysis (necropsy, tissue collection, fixation, IF, IHC, ELISA, PCR) as well as cell culture is beneficial but not necessary. etc. | 8/26/2020 |
| 765 | CRISPR Therapeutics Cambridge, MA Research Associate II/Sr. Research Associate, Analytical Development MS Exp: 1+ year(s) |
We are seeking a Research Associate to join an exciting, fast-growing and well-financed company to develop novel gene editing therapies for serious diseases. The successful candidate will join the Technical Operations (Tech Ops) group at CRISPR Therapeutics, focusing on development of analytical methods for ex vivo genetically modified cells to support the development of gene editing programs. The individual will develop quantitative assays measuring gene editing in target and non-target cells, cell-based assays measuring the expression and the biological functions of specific genes. The successful candidate will independently design, perform, and analyze experiments for multiple preclinical and clinical programs, and will work independently to support process development, product characterization, and technical transfer to CMOs and GMP test labs. etc. | 8/26/2020 |
| 766 | CRISPR Therapeutics Cambridge, MA Research Associate II/Senior Research Associate, Analytical Development (PCR/Genomics) MS Exp: 1+ year(s) |
We are seeking a Senior/Principal Research Associate to join an exciting, fast growing and well financed company to develop novel gene editing therapies for serious diseases. The successful candidate will join the Technical Operations (Tech Ops) group at CRISPR Therapeutics, focusing on development of analytical methods for ex vivo genetically modified cells to support the development of gene editing programs. The individual will develop and qualify PCR-based assays (qPCR and ddPCR) to measure gene editing in target and non-target cells, characterizing genome changes, as well as assays to measure viral genome titer. He or she will independently design, perform, and analyze experiments for multiple preclinical and clinical programs, and support process development and product characterization under guidance. etc. | 8/26/2020 |
| 767 | CRISPR Therapeutics Cambridge, MA Research Associate II/Senior Research Associate (Cell Based Assays) MS Exp: 1+ year(s) |
We are seeking a Research Associate II/Senior Research Associate to join an exciting, fast-growing, and well-financed company to develop novel gene editing therapies for serious diseases. The successful candidate will join the Technical Operations (Tech Ops) group at CRISPR Therapeutics, focusing on development of analytical methods for ex vivo genetically modified cells to support the development of gene editing programs. The individual will develop quantitative assays measuring gene editing in target and non-target cells, cell-based assays measuring the expression and the biological functions of specific genes. He or she will independently design, perform, and analyze experiments for multiple preclinical and clinical programs, and will work independently to support process development, product characterization, and technical transfer to CMOs and GMP test labs. | 8/26/2020 |
| 768 | CRISPR Therapeutics Cambridge, MA Research Associate II, Analytical Development MS Exp: 1+ year(s) |
We are seeking a highly organized Research Associate II to join an exciting, fast-growing and well-financed company to develop novel gene editing therapies for serious diseases. The successful candidate will join the Technical Operations (Tech Ops) group at CRISPR Therapeutics, with a multi-functional skill set, such as developing and managing primary cell banks, execution of assays, as well as building a sample management system. The sample management aspect will be concentrated on the use of databases, such as Microsoft Access, Excel, and SharePoint and aid in organizing and keeping track of samples and internal distributions, where there is opportunity for movement. The cell banking aspect will focus on generating cell banks by isolating and characterizing primary cells from donor samples, complete donor screening, and work independently to support process development and product characterization. etc. | 8/26/2020 |
| 769 | CRISPR Therapeutics Cambridge, MA Research Associate II, Analytical Development MS in a biological science Exp: 1+ year(s) |
We are seeking a Research Associate II to join an exciting, fast-growing, and well-financed company to develop novel gene editing therapies for serious diseases. The successful candidate will join the Technical Operations (Tech Ops) group at CRISPR Therapeutics, focusing on development of analytical methods for ex vivo genetically modified cells to support the development of gene editing programs. The individual will develop quantitative assays measuring gene editing in target and non-target cells, cell-based assays measuring the expression and the biological functions of specific genes. The successful candidate will design, perform, and analyze experiments for multiple preclinical and clinical programs, and will work to support process development, product characterization, and technical transfer to CMOs and GMP test labs. etc. | 8/26/2020 |
| 770 | Casma Therapeutics Cambridge, MA Research Associate, Biology MS in biology or related Exp: 1-3 year(s) |
We are seeking a highly motivated, Research Associate to participate in drug discovery programs that lead to the identification of new targets and drug candidates for clinical development. The individual should possess strong core competencies in cell biology, molecular biology, assay development. We are seeking a qualified candidate who will share our excitement about the science, contribute to our culture, and honor our commitment to patients. Responsibilities: Cell culture and cell line development using retro- and lenti-virus, CRISPR and downstream analysis of autophagy and signaling. Perform western blotting, FACS and imaging analysis to analyze autophagy and specific target activity in primary cells and cell lines. etc. | 8/26/2020 |
| 771 | BioLegend San Diego, CA Manufacturing Associate - Recombinant Protein Purification BS in a life science Exp: 1+ year(s) |
This position is responsible for manufacturing cutting edge recombinant protein research products in Molecular Cellular Immunology (MCI) manufacturing group. The Recombinant Manufacturing Associate will focus on recombinant protein purification. The duties include preparing buffer solutions, and purifying recombinant proteins to standard operating procedures. Another part of the job responsibility includes transferring the products to other groups, preparing product/project related documentation, and maintaining the production record for recombinant protein products. etc. | 8/18/2020 |
| 772 | BioLegend San Diego, CA Bottling Technician - Formulation Group (1st shift 8:00am - 4:30pm) HS diploma or equivalent Exp: 6-12 months |
BioLegend is looking for a Bottling Process Technician for our Formulation Group. This role will be responsible for processing product formulations, filling, capping, labeling, and completing batch records, and putting away Finished Good Inventory (FGI). This is a highly team oriented group which involves working closely with other core teams within the Bottling Department as well as other departments such as Planning, Receiving, Inventory Control, Custom Solution Team (CST), Packaging and Quality Control groups. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Assist in performing various bottling related tasks to include dispensing antibody solutions and capping and labeling of vials, tubes or bottles. etc. | 8/18/2020 |
| 773 | BioLegend San Diego, CA Packaging Technician HS diploma Exp: 6 months |
BioLegend is looking for an energetic Packaging Technician to work in our dynamic, fast paced warehouse environment. This position will entail picking a high volume of products based on orders processed and preparing them for shipment. This role involves a high degree of repetitive tasks with a focus on quality. Essential Functions: Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Picking vials for orders processed according to the pick ticket for each order, triple-checking the order for accuracy, preparing for shipping. Ensuring correct products are picked and processed. etc. | 8/18/2020 |
| 774 | BioLegend San Diego, CA Research Associate - Cell Analysis & Flow Cytometry BS/MS in a life science Exp: 1+ year(s) |
As a Research Associate, you will report to a Senior Scientist or Manager, where you will be able to conduct extensive analysis on new or existing products and consistently report key findings on product research initiatives. Under general supervision and with on-going review, this position researches, designs, develops and/or supports experiments for product development, process optimization applications, analytical methods, and validation activities ensuring a successful transition into a GMP manufacturing environment. The work requires routinely handling small animals and biological samples from animals and human donors. Prior experience in tissue culture, flow cytometry, immunoassays (eg ELISA, immunefluorescent/immune-histochemical staining, Western Blotting,), molecular biology techniques (eg PCR, cloning, etc.), data analysis, and project management are preferred. etc. | 8/18/2020 |
| 775 | BioLegend San Diego, CA Manufacturing Associate - Conjugation (2nd Shift 4:00pm - 12:30am) AS in biochemistry, chemistry, or related Exp: 1 year |
The Manufacturing Associate will be an integral member of a team that ensures the highest quality of our finalized antibody products. This position offers the opportunity to gain experience with different types of conjugation chemistries and different chromatography methods to purify antibodies and offers the opportunity to work in small scale to large scale product projects and to learn to utilize the (Enterprise Resource Planning) ERP database to track production schedules and deadlines and to enter production results. This position will also perform scale ups and perform troubleshooting of problematic products, including continuous improvement methodologies for efficiency. etc. | 8/18/2020 |
| 776 | BioLegend San Diego, CA Manufacturing Associate I - Purification (2nd Shift) BS in biology, biochemistry, chemistry, or other science Exp: 1+ year(s) |
The Manufacturing Associate position will function as an important member of the team that manufactures and provides antibodies and reagents to a diverse set of research areas including Immunology, Neuroscience, Cancer, Stem cells, and Cell Biology. This is a great opportunity for you to enhance your knowledge in the biotechnology industry. Essential tasks for this position include: following Standard Operating Procedures (SOP)s, creating and updating batch records, performing limited buffer preparation, cleaning glassware and restocking lab supplies. Additional responsibilities may also include processing troubleshooting and aliquoting bulk antibodies for finished goods inventory. etc. | 8/18/2020 |
| 777 | BioLegend San Diego, CA Manufacturing Associate I - Conjugation (Brilliant Violet Group) AS in biochemistry, chemistry, or related Exp: 1 year |
The Manufacturing Associate position for BioLegend’s Brilliant Violet (BV) Conjugation Group will be responsible for performing all essential functions related to antibody conjugation, including following SOPs and batch records and maintaining and analyzing lot histories. This individual will be an integral member of specialized team that ensures the highest quality of our highly successful BV antibody products, and will offer the opportunity to gain experience with different types of conjugation chemistries. Due to the light sensitive nature of these products, Associates will work in facilities with red lighting to ensure product quality. Associates will also learn different chromatography methods to purify antibodies, and have the opportunity to work in small scale to large scale product projects while learning to utilize the Enterprise Resource Planning (ERP) database to track production schedules and deadlines and to enter production results. etc. | 8/18/2020 |
| 778 | bioMerieux Lombard, IL Filling Operator I - Lombard, IL 1 HS diploma or equivalent Exp: 1 year |
As a Filing Operator 1, you will ensure goals are met through the understanding of objectives, communication with co-workers and supervisors, working safely, executing procedures, and ensuring the quality product is being manufactured. Employees are expected to stand for prolonged periods, perform basic mathematical equations, adhere to all verbal and posted guidelines, and be able lift up to 33lbs. Main Accountabilities: Perform packaging activities including but not limited to: label generation, visual inspection, heat sealing, and utilizing packaging equipment. Perform Filling activities in non-controlled areas: tube and bottle manufacturing. Perform routine cleaning tasks in relation to the manufacturing areas. Routinely checking inventory supplies and ensuring all levels are adequate. etc. | 8/18/2020 |
| 779 | bioMerieux Murray, UT Software Test Engineer I AS/BS in engineering, computer science, or equivalent Exp: 0-3 years |
The software test engineer works aside the software team to assist in producing quality software. This position is responsible for the design, implementation and execution of tests to verify that software and firmware operate correctly and meet design specifications. This individual should work creatively to automate testing where feasible. This individual should have knowledge of one or more programming languages. This engineer is expected to work and communicate well with other members, team leadership as well as company management in order to meet the goals of the project. Principal Job Duties and Responsibilities: Perform all work in compliance with company policy and within the guidelines of the bioMérieux Quality System. If in a leadership role – is responsible for leading and managing the portions of the project to which he/she is assigned as a leader to accomplish the goals of the project. etc. | 8/18/2020 |
| 780 | Bio-Rad Irvine, CA Tech Sup Rep I BS/AS Exp: 1-2 year(s) |
Responsible for providing technical support via phone and e-mail to external and internal customers, product support, R&D, marketing and sales group, selling units, distributors and other manufacturers for all QSD products. Includes familiarity with all QSD products, manage and analyze data, work with Customer Contact Report database, Unity/QCNet, and all other supporting programs. etc. | 8/18/2020 |
| 781 | Bio-Rad Irvine, CA R&D Technical Associate HS diploma or equivalent Exp: 0-2 year(s) |
Bio-Rad is looking for a Technical Associate to work in the R&D Development group. The position requires a limited working knowledge of laboratory experimentation, general chemistry, and clinical chemistry. This position will assist and support the development of clinical chemistry controls. The ideal candidate will also possess abilities in data entry/input, and is comfortable working with blood, serum, urine and/or their various components. Responsibilities: Support product development activities through execution of simple routine laboratory tasks. etc. | 8/18/2020 |
| 782 | Bio-Rad Irvine, CA Field Service Engineer AS/BS in electronics or related Exp: 0-2 year(s) |
Bio-Rad is seeking a Field Service Engineer who will perform repairs, upgrades, and preventive maintenance on our instruments for clinical diagnostics, life science, and biopharma customers based in the Washington DC area traveling 50 – 75%. Responsibilities: Provide customer site service on all CDG/LSG products including emergency service. Maximizes system uptime through proactive preventive maintenance. Act as customer advocate to ensure satisfaction and repeat business. Maintains company assets including parts inventory and leased vehicle. etc. | 8/18/2020 |
| 783 | BioReference Laboratories Elmwood Park, NJ Medical Lab Technician or Technologist, Hepatitis BS in medical technology, chemistry, biology or related Exp: 1 year |
The Medical Laboratory Technician will perform all necessary laboratory testing in the detection, diagnosis, and prognosis of disease. The Medical Laboratory Technician 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. Duties may include but are not necessarily limited to the following: Follows written lab procedures for the correct handling and processing of specimens. Performs lab procedures of moderate and high complexity in accordance with standards set forth in sectional laboratory procedures. etc. | 8/18/2020 |
| 784 | BioReference Laboratories Columbus, OH TEMP Medical Lab Technician or Technologist BS in medical technology, chemistry, biology or related Exp: 1 year |
The Medical Laboratory Technician will perform all necessary laboratory testing in the detection, diagnosis, and prognosis of disease. The Medical Laboratory Technician 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. Duties may include but are not necessarily limited to the following: Follows written lab procedures for the correct handling and processing of specimens. Performs lab procedures of moderate and high complexity in accordance with standards set forth in sectional laboratory procedures. etc. | 8/18/2020 |
| 785 | BioReference Laboratories Elmwood Park, NJ Medical Lab Technician or Technologist, Microbiology (FT, 40 Hours) BS in medical technology, chemistry, biology or related Exp: 1+ year(s) |
The Medical Tech performs all laboratory procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. Duties may include but are not necessarily limited to the following: Maintain standards in routine & STAT testing. Complete work in a timely manner. Write legibly when documenting QC, problems or information. etc. | 8/18/2020 |
| 786 | BioReference Laboratories Elmwood Park, NJ Medical Lab Technician or Technologist, Overnight (FT, 40hrs per week) BS in medical technology, chemistry, biology or related Exp: 1+ year(s) |
The Medical Tech performs all laboratory procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. Duties may include but are not necessarily limited to the following: Maintain standards in routine & STAT testing. Complete work in a timely manner. Write legibly when documenting QC, problems or information. etc. | 8/18/2020 |
| 787 | LGC Novato, CA GMP Manufacturing Tech 1- Weekend 3x12 Fri-Sun BS/BA Exp: Not necessary for bachelor's candidates |
The GMP Manufacturing Technician I position is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements as directed by the departmental supervisor, manager or director. To perform this job successfully, an individual must be able to perform each essential function satisfactorily. Essential Functions: Perform manufacturing activities according to written protocols, as directed by the departmental supervisor, manager or director. Maintain batch records, equipment logs and other production records as directed per company procedures. Maintain a clean an orderly laboratory environment. etc. | 8/18/2020 |
| 788 | LGC Novato, CA GMP Manufacturing Technician I BS/BA Exp: Not necessary for bachelor's candidates |
The GMP Manufacturing Technician I performs tasks associated with the production of modified oligonucleotides in a high throughput time sensitive manufacturing environment. A GMP Manufacturing Technician I may be called upon to work in any production shift in the GMP Manufacturing Department. Areas of Responsibility: Performs all assigned job functions per documented procedures as directed by Supervisor. Performs daily equipment and lab maintenance tasks. Able to follow all documented procedures. Other duties as assigned. etc. | 8/18/2020 |
| 789 | LGC Petaluma, CA Production Technician I, Oligo Liquid Handling BS in chemistry or life science Exp: 0-1+ year(s) |
A Production Technician I, Oligo Liquid Handling is responsible for performing day to day production activities in the custom oligonucleotide (oligo) Liquid Handling lab. Production activities will be performed in a timely fashion and in compliance with company procedures. The Liquid Handling team is responsible for ensuring oligos meet all customer specifications, and final processing prior to delivery to the customer. Areas of Responsibility: Performs all assigned job functions per documented procedures as directed by supervisor. Processes oligo samples in a high throughput production environment using automated Tecan liquid handlers. etc. | 8/18/2020 |
| 790 | Bioserv San Diego, CA Manufacturing Technician I/II HS diploma or equivalent Exp: 1-2 year(s) |
The Manufacturing Technician is responsible for supporting and performing routine procedures associated with the manufacture of the customer’s product with minimal direction from Supervisor. Manufacturing Technicians responsibilities include performing environmental monitoring, cleaning and sterilizing of glassware, cleaning of clean-room suites, manufacturing preparatory activities and clean-up, assist in formulation, visual inspections, labeling and packaging. They may be aseptically qualified to perform aseptic manufacturing set-up, filtration, filling and closure of product. With sufficient Bioserv training, they may be a primary operator of complex equipment and processes, and additional tasks that are assigned by Management in compliance with QSR’s, SOP’s, and written procedures with direction from the Project Coordinator and/or Supervisor. etc. | 8/18/2020 |
| 791 | Bioserv San Diego, CA Manufacturing Technician I HS diploma or equivalent Exp: 1-2 year(s) |
Under direct supervision, the Manufacturing Technician I will be responsible for supporting and performing routine procedures associated with the manufacture of the customer’s product. This individual will work independently once they are trained and experienced with technician tasks. Essential Duties & Responsibilities: Perform environmental monitoring and complete documents associated with the activity. Clean and sterilize glassware and other materials. Perform cleaning of cleanroom suites. etc. | 8/18/2020 |
| 792 | Bioventus Tampa, FL Associate Sales Rep - Biomedical - Tampa, FL BS/BA in sports medicine, life science or a commercial discipline Exp: 0-2+ year(s) |
The Associate Sales Representative (ASR) is an entry level sales role at Bioventus. The ASR is primarily responsible for consulting with and providing clinical and technical information to healthcare professionals and their staff to achieve the sales objectives. Associate Sales Representatives will operate within company policies and procedures and demonstrate a high degree of compliant and ethical behaviors. Successful candidates should be open to relocation, at least to bordering states. Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. etc. | 8/18/2020 |
| 793 | Bioventus Stamford, CT Associate Sales Rep - Biomedical - Stamford, CT BS/BA in sports medicine, life science or a commercial discipline Exp: 0-2+ year(s) |
The Associate Sales Representative (ASR) is an entry level sales role at Bioventus. The ASR is primarily responsible for consulting with and providing clinical and technical information to healthcare professionals and their staff to achieve the sales objectives. Associate Sales Representatives will operate within company policies and procedures and demonstrate a high degree of compliant and ethical behaviors. Successful candidates should be open to relocation, at least to bordering states. Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. etc. | 8/18/2020 |
| 794 | Blueprint Genetics Seattle, WA Medical Technologist BS in a biological, chemical, or physical science Exp: 1 year |
The Medical Technologist performs tests requiring the exercise of independent judgment and responsibility in those specialties in which the Technologist is qualified by education, training and experience. In addition, the Medical Technologist is responsible for assuring that a given test system is operated in accordance with the laboratory's procedure manual and that the applicable quality control requirements are met. The incumbent actively supports and complies with all company and departmental policies and procedures. etc. | 8/18/2020 |
| 795 | BlueRock Therapeutics Cambridge, MA Research Associate I/II, Genome Sciences BA Exp: 0-5 years |
We are seeking a research associate to join our newly formed Genome Sciences team in Cambridge. Reporting to the Scientist, she or he will play a central role in the development, production, and evaluation of CRISPR gene editing components for use in pluripotent stem cells. The qualified candidate will have solid experience in expression and purification of recombinant proteins from bacterial cell culture and have some proficiency with mammalian cell culture using aseptic technique. He or she will also be curious, innovative, persistent, and be able to work independently in the laboratory with minimal supervision. etc. | 8/18/2020 |
| 796 | Boston Analytical Framingham, MA Environmental Monitoring Technician HS diploma/AA/AS Exp: None required |
The 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. Primary Duties and Responsibilities: Collects routine daily, weekly and monthly EM samples in pharmaceutical cleanrooms. Sample types include air viable, surface viable, and air nonviable monitoring. Collects compressed gas samples to ensure they are free of microbial and chemical contamination. Samples purified water system at both generation and point of use for subsequent analysis for Bioburden, TOC, Conductivity, and Endotoxin. etc. | 8/18/2020 |
| 797 | Boston Analytical Salem, NH QA Specialist – All Levels BS in a scientific discipline Exp: 0-3 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. Primary Duties and Responsibilities: Auditing chemists’ routine project folders for conformance to company and customer requirements. Write, review and edit Standard Operating Procedures (SOP’s, Forms and Methods) and familiarity with internal SOPs. Alternate contact person for QA questions relating to laboratory operations and client correspondences. Work with area management on the writing, issuance and tracking of deviations and investigations for closure. Perform and assist with GMP audits. etc. | 8/18/2020 |
| 798 | Boston Analytical Salem, NH Scientist II – Method Development and Validation MS in chemistry or related Exp: 1+ year(s) |
The Scientist II conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. The position includes development of analytical methods and attendant procedures, as well as validation of analytical methods, including writing validation protocols and reports. Techniques will include analysis of pharmaceutical products using chromatographic techniques, spectrographic techniques, thermal analysis, and wet chemical analysis. Primary Duties and Responsibilities: Develops methods based on client requirements. Specific techniques include, but are not limited to HPLC, GC, AA, FTIR, and dissolution. Conducts research on manufactured products to develop, improve and validate test procedures. Validates methods compliant with regulatory requirements. etc. | 8/18/2020 |
| 799 | Boston Analytical Salem, NH Microbiologist II BS in microbiology or related Exp: 1-5 year(s) |
The QC 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. Primary Duties and Responsibilities: Prepares and analyzes samples to determine microbiological quality through the following analyses: Microbial enumeration methods, absence of specified microorganisms, endotoxin, and water quality analysis (bioburden, TOC, Conductivity). Performs genetic analysis of microbial growth to determine Genus/Species of unknown isolates. Collects Environmental Monitoring Samples onsite and offsite at client manufacturing sites. Documents work in a clear and organized manner. etc. | 8/18/2020 |
| 800 | Boston Scientific Quincy, MA Inspector II - Incoming Inspection 1st shift Job HS diploma or equivalent Exp: 1-2 year(s) |
To perform inspection activities on products and to release products to Finished Goods or other release locations; control of products through such activities as inspection of new product lines to Finished Goods, processing shipping holds, processing/controlling pre-release product lines, processing scrap, processing quality records, processing Returns product inspection. Your responsibilities include: Perform inspection activities on products, in such categories as sterility inspection, incoming inspection, in process inspection and returns inspection. Complete data forms with the results of inspection activities, including non-conforming material reports, when required. SAP & WM transactions related to inspection activities. Insure completion of nonconforming reports and update the MRB system. etc. | 8/18/2020 |
| 801 | Boston Scientific Arden Hills, MN Process Technician III Job AA/AS Exp: 1+ year(s) |
This position works independently to assist R&D and process engineers, scientists, and/or teams in the development and analysis of products, materials, processes, or equipment. Your Responsibilities Will Include: Participate in the operation and maintenance of process equipment. Develop concepts and accordingly construct prototypes/products from concepts. Explore and propose creative solutions based on solid rationales and contribute to design and process concepts. Organize, coordinate, and execute building and testing of prototypes/products per engineering instructions. etc. | 8/18/2020 |
| 802 | Boston Scientific Maple Grove, MN Machine Operator I - 1st Shift - Maple Grove, MN--Extrusion Job AS/AA Exp: 1 year |
Primary focus is to build quality product by following processes to meet all production goals. Your Responsibilities Include: Understands and adheres to safety policies and practices. Responsible for quality and adheres to manufacturing process requirements, the Boston Scientific Corporation Quality Policy and the Strategic Quality Process (SQP). Builds product by following all processes in which certified (in their most current revision), and completes other assigned work, while meeting manufacturing goals a8nd metrics. Gains basic understanding of Lean Manufacturing and related principles. Willing to flex and rotate as necessary and work well with all group members, both within the team and cross-functionally. etc. | 8/18/2020 |
| 803 | Boston Scientific Maple Grove, MN Manufacturing Technician II (2nd Shift) Job AA/AS Exp: 0-3 years |
With general supervisory direction, assist in the daily support of products, processes, materials, and equipment in order to achieve production goals (i.e., quality, delivery, cost, productivity, and safety). Maintenance activities for automated PC and PLC controlled manufacturing equipment. Identify and troubleshoot process, material or equipment problems to minimize down time and improve process yields. Identify, design, and implement process equipment changes to improve reliability of the process. Modify existing and develop new tooling and fixtures. Revise existing documents, processes, and/or methods to correct or improve processes/product. Work with vendors/suppliers to procure and install tooling, fixtures, and/or equipment. etc. | 8/18/2020 |
| 804 | Boston Scientific Maple Grove, MN Manufacturing Technician II (3rd Shift) Job AA/AS Exp: 0-3 years |
With general supervisory direction, assist in the daily support of products, processes, materials, and equipment in order to achieve production goals (i.e., quality, delivery, cost, productivity, and safety). Your Responsibilities Will Include: Maintenance activities for automated PC and PLC controlled manufacturing equipment. Identify and troubleshoot process, material or equipment problems to minimize down time and improve process yields. Identify, design, and implement process equipment changes to improve reliability of the process. Modify existing and develop new tooling and fixtures. Revise existing documents, processes, and/or methods to correct or improve processes/product. etc. | 8/18/2020 |
| 805 | Boston Scientific Maple Grove, MN Manufacturing Engineer I Job BS in engineering Exp: 0-2 year(s) |
Your Responsibilities Will Include: Provides daily support of production, processes, materials and equipment in order to achieve NSM department goals (i.e. safety, quality, delivery, and cost). Works cooperatively with R&D, Process Development, Quality, Production, Regulatory, Equipment Engineering, Supply Chain, and Marketing to ensure project success. Successfully contributes to both new product development teams and product support, typically including the following activities: process capability studies, process development, Six Sigma and Value Improvement projects, report preparation and process/test documentation. Designs and coordinates standard engineering tests and experiments. Designs, procures, and fabricates equipment tooling and fixtures. etc. | 8/18/2020 |
| 806 | Boston Scientific Quincy, MA Industrial Engineer I - Defined Term Job BS in industrial, mechanical, or manufacturing engineering Exp: 6+ months |
The Industrial Engineer is responsible for working with key business partners to drive value improvement guided by lean principles to support business strategy and priorities. The Industrial Engineer will also develop/implement continuous process improvement to ensure efficient and cost effective workflows/practices in a light manufacturing and distribution environment. Your responsibilities include: Assess process capabilities, prioritize process improvement opportunities, and innovate and implement process improvements on multiple and moderately complex processes. Coordinate and lead facility layout and design projects within business units. Coordinate and champion value improvement projects throughout the business. Conduct Lean training programs for employees at all leves and departments. Actively deploy and coach the organization on Lean and LBP Essentials. etc. | 8/18/2020 |
| 807 | Bristol Myers Squibb Phoenix, AZ Operator I, Aseptic HS diploma or equivalent Exp: 1 year |
The Operator I is responsible for executing production activities required to successfully manufacture sterile injectable products. This is accomplished by ensuring equipment, materials, and other resources are in place to meet production demands. The Operator I demonstrates and assures production activities within manufacturing operations are executed following all GMP’s. In addition, work will be performed in complete accordance with all SOPs, Specifications, Batch Records, regulatory expectations, and company policies. This position will require overtime, shift work, and flexibility in scheduling of “set” shift hours at times, based on production demands or extraordinary circumstances. etc. | 8/18/2020 |
| 808 | Bristol Myers Squibb Syracuse, NY Assistant Scientist BS in a biological science Exp: 0-3 years |
Duties/Responsibilities: Perform laboratory analysis of samples, using aseptic technique, following established procedures and in full compliance with official compendial, health authority regulations, and established BMS policies. Conduct qualification of methods and/or other laboratory studies, according to scientific protocols. Maintains accurate records of work performed and documents results, according to Good Documentation Practices and established procedures as well as perform data entry into LIMS, MODA and LES. Assist with review of worksheets and laboratory data as assigned. Assists in the investigation of OOS results in areas of assigned responsibility. Operates and maintains laboratory instruments, while ensuring the reliability of instrumentation through proper maintenance, with ability to troubleshoot minor issues. Must analyze, evaluate, and interpret data, notifying clients of results, and assisting to resolve issues, if applicable. etc. | 8/18/2020 |
| 809 | Bristol Myers Squibb Syracuse, NY Dispensary Warehouse Technician I BS/BA Exp: 1+ year(s) |
The primary role of the Dispensary Warehouse Technician is to perform functions relevant to Warehouse, Dispensary, and staging activities in the manufacturing facility. Core functions include Receiving materials, Material Transfers, SAP functions for inventory control, dispensing, material returns, and raw material sampling. Related activities include supply upkeep, cleaning, and bulk chemical transfers. All operations are to be performed in a safe and compliant manner. Duties/Responsibilities: Accurate receipt and unpacking of all process related direct inventory materials, indirect supplies, miscellaneous equipment, and material transfers. Including wipe down processes, SAP transactions, and proper storage adherence. Material transfers and movements from location to location. etc. | 8/18/2020 |
| 810 | Bristol Myers Squibb Summit, NJ Manufacturing Associate, CAR-T BS/BA Exp: Not necessary for bachelor's candidates |
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. Duties and Responsibilities: Production of blood component lots through selection, activation, transduction, cell culture, harvest, and cryopreservation. Aseptic technique is required for most activities: tube welding, connections, and transfers, at minimum. Weighs and measures in-process materials to ensure proper quantities are added/removed. Adheres to the production schedule ensuring on-time, internal production logistics. etc. | 8/18/2020 |
| 811 | Icon Raleigh, NC Associate Project Manager Translations BS/BA in languages/translations Exp: 1-3 years in translation |
As Translation Associate Project Manager you are responsible for the coordination, execution, control and completion of single service projects ensuring consistency with ICON SOPs, service-line best practices, project contracts and budgets. Lead the planning and implementation of single service projects. Define project tasks and resource requirements based on project plans | 8/16/2020 |
| 812 | Icon Knoxville, TN CRA I BS/Ba Exp: 12 months as an independent monitor |
As a Clinical Research Associate I at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - III, ensuring adherence to applicable regulations and principles of ICH-GCP. | 8/16/2020 |
| 813 | Icon Raleigh, NC Proposals Development Assoc II BS/BA in sciences or business Exp: 1-3 years within CRO, Pharma or Healthcare |
This particular role would support our Laboratory Services Division. As a Senior Proposals Development Associate you will support Business Development in the winning of new business for ICON Laboratory Services through delivery of high quality customer-focused proposals and budgets for the conduct of clinical trials in response to Requests for Proposals (RFPs). | 8/16/2020 |
| 814 | Icon Wilmington, NC CRC Assistant BS/BA in sciences/healthcare Exp: 1-3 years |
Performs study start-up duties including the production of a recruitment tool, and progress notes, as well as phone screening patients and identifying participants for trials on site. Proactively develops and executes recruitment plans that meet and exceed enrollment goals. Completes training on Clinical Trial Management System and maintains proper skills to update database, complete participant reimbursement, capture referral source of participants, and create calls lists to promote recruitment. | 8/16/2020 |
| 815 | Icon Raleigh, NC Clinical Research Associate II BS/BA in healthcare/sciences Exp: 12-18 months as independent monitor as CRA |
As a Clinical Research Associate at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP. | 8/16/2020 |
| 816 | ICU Medical Salt Lake City, UT Repair Technician - temp/entry level HS Diploma/GED or AS in technical discipline Exp: 0-2 years |
The Service Hub Technician is responsible for triaging devices where critical decisions are made on the PCI, repair, updating of service record, tracking labor and material as well as updating and printing of a Service Report that is returned with the repaired device. | 8/16/2020 |
| 817 | ICU Medical Salt Lake City, UT Material Handler M-F 6-2:30 HS Diploma/GED Exp: 1 year in warehouse/material handling |
The Material Handler supports Production by moving, transferring and pulling orders needed to support Production. The Material Handler performs inventory transactions in Oracle and delivers products to production to complete work orders. Operate Forklift, Walkie Rider, Order selector or pallet jack as needed to provide materials to Production areas | 8/16/2020 |
| 818 | ICU Medical Austin, TX Instrumentation & Calibration Technician Associates in sciences/technology/engineering Exp: 0-3 years in instrumentation/calibration |
Calibrate instruments and devices in the calibration and preventive maintenance program. Resolve complex repetitive instrument problems. Assist Calibration supervisor in determining preventive maintenance and calibration programs/maintenance procedures are followed. Trouble-shoot and repair instruments and systems. | 8/16/2020 |
| 819 | IGM Biosciences Mountain View, CA Research Associate / Senior Research Associate, Biomarkers MS in relevant Exp: 1+ years in industry/academia |
Our Preclinical Sciences group is looking for a Research Associate with a background in Immunology, Cell Biology or a related scientific discipline to join our growing and friendly team during this exciting time in our expansion. Duties include: Human and mouse cell culture and primary cell maintenance and isolation. Design, develop and execute in vitro cell-based immunoassays. | 8/16/2020 |
| 820 | iHear San Leandro, CA Audiologists/Hearing Care Professionals, Hearing Aid Startup Degree in audiology Exp: 1 year in hearing aid dispensing |
Working with research & development, sales, and customer support with issues related to product, inquiries, orders, fulfillment and post sales support. Help establish systems and procedures for professional support. Provide audiology or dispensing knowledge to the organization. Provide customers with support regarding product selection, programming of our proprietary hearing devices, web-applications, software installations, etc. | 8/16/2020 |
| 821 | Illumina Foster City, CA Research Associate I Fluidic Systems BS or MS in chemical/bio engineering Exp: 1-2 years in R&D |
Conduct focused research and development under general direction of supervisor to plan, conduct, analyze, interpret, and report recommendations based on experimental results in routine setting. Develop new sequencing applications, assay workflows and assay automation methods. Plan controlled experiments to characterize key components and finished reagents | 8/16/2020 |
| 822 | Illumina Foster City, CA Equipment Engineer I-II (1st Shift) Bs or MS in engineering/sciences Exp: 1-5 years in CxP lab |
The Equipment Engineer I-II will be responsible for integration, implementation, service and maintenance of laboratory equipment. This will include automation and instrumentation in support of a Clinical, Research and various GxP Laboratories.This includes installation, configuration and repair of equipment, integrating equipment with information systems and validation and verification of the equipment in accordance with CLIA, cGMP and/or GLP guidelines. | 8/16/2020 |
| 823 | Illumina Foster City, CA Engineer 1 - Fluidic Systems MS in mechanical engineering, bioengineering, or physics Exp: 1-2 years in lab environment |
As an Engineer 1 in the Research and Technology Development department, you will support the development of novel microfluidic-based sequencing platforms. You will be part of a multidisciplinary team solving complex problems, investigating new research areas and working on integration challenges. | 8/16/2020 |
| 824 | Illumina San Diego, CA Manufacturing Specialist 1 BS/BA in related Exp: 0-1 years |
Able to formulate All Scale reagents under detailed direction of Work Instruction and ensure production order meets QC functional testing requirements and acceptance criteria. Quality review and release of Manufacturing DHRs for Reagents and Consumables in CamStar; Facilitate and help the manufacturing team resolve batch record data discrepancies | 8/16/2020 |
| 825 | Illumina San Diego, CA Research Associate 2 BS in engineering or sciences Exp: 1-2 years in wet lab experience |
As a Research Associate 2 at Illumina in Systems Integration, you will work in a dynamic, team-oriented environment and help create genomic analysis tools used in the leading edge of research to advance human health by unlocking the power of the genome. Hands-on testing and integration of systems - hardware, software, chemistry, and application components | 8/16/2020 |
| 826 | Illumina Madison, WI Quality Ops Analyst BS/BA in sciences Exp: 0-3 years in FDA/ISO regulated industry |
This position is responsible for performing Quality Assurance activities and is accountable for ensuring compliance with established procedures and requirements. This individual is authorized and designated by Illumina to conduct quality inspections of product and associated documentation to ensure compliance with established procedures and requirements | 8/16/2020 |
| 827 | Imarc Minnetonka, MN Clinical Research Associate BS/BA in science, engineering or RN Exp: 18 months in clinical research |
The primary focus of this position is on routine monitoring and management of the research-related activities at a clinical site. Once fully trained, a Clinical Research Associate will be expected to perform site initiation, periodic, and close-out visits. Additionally, the Clinical Research Associate will be expected to serve as a resource and research liaison between assigned sites and the Sponsoring companies or CROs. | 8/16/2020 |
| 828 | Imarc Strongsville, OH Clinical Research Associate BS/BA in science, engineering or RN Exp: 18 months in clinical research |
The primary focus of this position is on routine monitoring and management of the research-related activities at a clinical site. Once fully trained, a Clinical Research Associate will be expected to perform site initiation, periodic, and close-out visits. Additionally, the Clinical Research Associate will be expected to serve as a resource and research liaison between assigned sites and the Sponsoring companies or CROs. | 8/16/2020 |
| 829 | Immucor Norcross, GA Medical Laboratory Technologist Associates or BS/BA Exp: 6-12 months related experience |
As a Medical Technologist, you will perform all assigned tasks following applicable laboratory SOPs, OSHA regulations and cGMP regulations (i.e. blood borne pathogens and chemical hazards). You will assist the department supervisor and/or manager with investigations, root cause analyses, and reports of out-of-specification results and deviations. You will also be responsible for maintaining and compiling Device History Records. | 8/16/2020 |
| 830 | Immucor Warren, NJ Manufacturing Associate Assocites Exp: 1 year in cGMP manufacturing |
As the Manufacturing Associate, you will perform setup, operation, re-supply, documentation, cleaning, minor equipment adjustments and minor preventative maintenance tasks to meet standards for safety, quality and efficiency. Formulating custom bulk reagents - involves working with pipettes and balances | 8/16/2020 |
| 831 | Immucor Norcross, GA Production Technician HS Diploma/GED or AS in technical discipline Exp: 0-2 years in clean room environment |
As a Production Technician, you will perform tasks and administrative aspects regarding packaging operations according to department procedures, specifications or work instructions. This includes starting up/breaking down operations, clearing operations areas, calculating component usage, verifying counts of products in and out of operations, and visual inspections of products for defects. | 8/16/2020 |
| 832 | Immucor Norcross, GA Supply Chain Analyst BS/BA in engineering Exp: 1-3 years in related |
As a Supply Chain Analyst, you will use analytical and quantitative methods to understand, predict, and enhance supply chain processes by assembling data, analyzing performance, identifying problems, and developing recommendations to support SCM planning and manufacturing operations. | 8/16/2020 |
| 833 | Immucor Warren, NJ Manufacturing Associate Associates degree Exp: 1 year in cGMP manufacturing |
As the Manufacturing Associate, you will perform setup, operation, re-supply, documentation, cleaning, minor equipment adjustments and minor preventative maintenance tasks to meet standards for safety, quality and efficiency. Formulating custom bulk reagents - involves working with pipettes and balances | 8/16/2020 |
| 834 | Immucor Norcross, GA Production Technician HS Diploma/GED or AS in technical discipline Exp: 0-2 years in clean room environment |
As a Production Technician, you will perform tasks and administrative aspects regarding packaging operations according to department procedures, specifications or work instructions. This includes starting up/breaking down operations, clearing operations areas, calculating component usage, verifying counts of products in and out of operations, and visual inspections of products for defects. | 8/16/2020 |
| 835 | Immucor Waukesha, WI Production Chemist BS/BA in chemistry/life sciences Exp: 0-2 years working with automated filling equipment a plus |
As Production Chemist, you will be responsible for subassembly formulation, raw material preparation and/or processing, QC testing reagent or component formulation, and some in-process testing. You will manage the development, planning, and implementation of manufacturing methods, processes, and operations for new or existing products or technologies. | 8/16/2020 |
| 836 | Immune technology Corp New York, NY Sales Associate BS/BA in life sceinces Exp: 1 year in sales/marketing |
Full/part time position, responsible for ensuring customer retention through account management and increasing revenue through marketing activities and generation of sales leads. Establishing and retaining customer relationships primarily through phone, e-mail and personal visit. Delivering requested documents, literature, and information to customers | 8/16/2020 |
| 837 | Bayer Creve Coeur, MO Production Associate BS/BA Exp: 1+ year(s) |
The primary responsibilities of this role, Production Associate, are to: Embrace and demonstrate a safety-first culture at all times; Perform daily operations as directed by site leadership; Be accountable for safe and timely delivery of quality supply based on production schedules while maintaining an efficient operation; Perform duties in a manner that support overall site Key Metrics including Safety, Quality, TIP (total individual volume performance), TOP (total overall volume performance) and cost efficiency; etc. | 8/11/2020 |
| 838 | Bayer Berkeley, CA Production Specialist III CCTC MS Exp: Not necessary for MS candidates |
The primary responsibilities of this role, Production Specialist III of Cell Culture Technology Center (CCTC), are to: Be responsible for all aspects of clinical manufacturing in the following areas such as Cell Expansion, Cell Culture, Purification, Solution Preparation and Weigh/Dispense and work seamlessly across all areas and will be an SME for NLT one area; Participate in new products introductions (NPIs) into CCTC with support from BD and MSAT; Ensure all activities are performed to schedule; Act as delegate to Senior Production specialist; Collaborate with BD and MSAT to ensure cross functional alignment with platform process, equipment, raw materials and/or automation for NLT one area; etc. | 8/11/2020 |
| 839 | Bayer Jerseyville, IL Agronomic Research Specialist MS/MA Exp: 0-2 years |
The primary responsibilities of this role, Agronomic Research Specialist II, are to: Be responsible for the implementation of unique and innovative technology solutions designed to improve research design and operations success through the use of new tools and methodologies to improve overall plant breeding phenotyping such as the pilot and use of geospatial systems, agronomic planting and harvesting tools, harvesting shelling systems and data capture applications; Collaborate with project team members to deliver detailed experimental protocols that enable advancement decisions by our scientists and placement decisions to our customers; etc. | 8/11/2020 |
| 840 | Bayer Kansas City, MO R&D Specialist II-Product Support MS in chemistry, biology, engineering or related Exp: Not necessary for MS candidates |
The primary responsibilities of this role, R&D Specialist II, are to: Provide development expertise for new formulations by providing Pilot Scale knowledge and advise and Startup assistance for production plants; Assist Product Supply and Supply chain by performing studies related to product quality and assurance of supply; Prioritize and can coordinate work within a large team; Provide training to third party reports; Maintain detailed record keeping and required documentation; Be accountable for cross-functional work within platform and/or across process areas; etc. | 8/11/2020 |
| 841 | Bayer Saxonburg, PA Assembler I Day Shift 6am-6pm HS diploma or equivalent Exp: 1+ year(s) |
The primary responsibilities of this role, Assembler I, are to: Assemble various products; Package various products; Perform rework and inspection on the product; Back up higher-level positions; Have awareness of quality standards and ability to identify defects in products; Record data related to product quality and traceability; Clean of work areas as required; etc. | 8/11/2020 |
| 842 | Bayer Kearney, NE Production Associate BS/BA Exp: 1+ year(s) |
The primary responsibilities of this role, Production Associate, are to: Embrace and demonstrate a safety-first culture at all times; Perform daily operations as directed by site leadership; Be accountable for safe and timely delivery of quality supply based on production schedules while maintaining an efficient operation; Perform duties in a manner that support overall site Key Metrics to include: Safety; Quality, TIP (total individual volume performance), TOP (total overall volume performance), and cost efficiency; Embrace an environment that promotes the building of good working relationships within the site; Participate in the execution of HSE, Quality Management System (QMS) and One PSS programs and elements; participates in associated networks; Contribute in plant operations such as conditioning, packaging, lab operations, warehouse / inventory management / distribution, carryover, etc., as assigned by the site leadership team; etc. | 8/11/2020 |
| 843 | Bayer , OH Field Sales Rep I BS/BA Exp: 1+ year(s) |
As a Field Sales representative for Channel, you will be responsible for growing the market share of Seed & Trait business within Northwest Ohio covering the counties of Darke, Mercer, Van Wert, Paulding, Defiance, Henry Putnam, Allen, Auglaize, Shelby, Logan, Hardin, and Union. In this position, you will create demand for Bayer seed growth and Seed & Trait chemistry products through retailers, dealers, and top growers. The primary responsibilities of this role, Field Sales Representative I, are to: Develop and implement dealer business plans, manage forecasting, inventory management and product line demand issues, set the business direction, and coordinate follow-ups with dealers; Serve as the key business consultant to retailers and dealer and effectively sell the value of Bayer crop science products; etc. | 8/11/2020 |
| 844 | Beckman Coulter Diagnostics Chaska, MN Scientist I Production Operations BS in biology, microbiology, or related Exp: 0-2 years |
Key Responsibilities: Read, comprehend and follow established work instructions and procedures with emphasis on quality. Execute the daily production plan to due date conformance and quality standards. Train to Standard Operating Procedures (SOPs). Follow engineering drawings, work order information, SOPs, and other written and verbal specifications in the manufacturing process while maintaining FDA requirements. Handle a variety of cell lines with a strict attention to detail while working aseptically. Independently execute work regarding maintenance of cell cultures, processing cellular material and releasing builds according to schedule. Apply basic analytical skills, critical thinking and scientific methods to perform daily tasks. Perform the set-up, calibration, testing and troubleshooting of instruments, such as large-scale bioreactor systems. Assure compliance with FDA Quality System Regulations (QSR), Good Manufacturing Practices (GMP), and ISO regulatory requirements. etc. | 8/11/2020 |
| 845 | Beckman Coulter Diagnostics Chicago, IL Field Service Engineer - Laboratory Instrumentation and Automation: Chicago AS/BS Exp: 1-3+ year(s) |
Beckman Coulter Diagnostics Field Service Engineers provide excellent customer service to clients while installing and maintaining diagnostic instrumentation and systems in hospital and stand-alone laboratory environments. As a Field Service Engineer (FSE) you will be the face of Beckman Coulter to customers and support them, directly impacting patient health and overall well-being. Would you like to be part of a team providing front line support to hospital laboratories? Are you ambitious and seeking to drive healthcare forward? The Field Service Engineer in this position will: Under minimal supervision, serve as lead to assigned customers; complete troubleshooting, installation, validation, maintenance, and service repair needs on designated equipment. May assist and/or train newer Field Engineers. Provide excellent and efficient service to Beckman Coulter’s customers, along with technical training on products. Repair, maintain, and install product line(s). etc. | 8/11/2020 |
| 846 | Beckman Coulter Diagnostics Miami, FL Biomedical Customer Technical Support AS/BS in biology, biomedical engineering, electrical engineering, chemistry, or related Exp: 1-2 year(s) |
1st, 2nd or 3rd shift positions. Will require rotating weekends, holidays and to backfill vacation requests for other team members. Provide general technical consulting to customers and company staff distinguishing among hardware, reagent and software issues in order to resolve or dispatch the appropriate resource at minimum company expense. Associate will work in the Miami, Florida campus. Primary Duties and Responsibilities: Fielding Customer Calls to Facilitate 24/7 Support Function. Through telephone and electronic (i.e. email) technology provide resolutions on Hardware, Software, Assay and Training related calls from existing customer base. Measured on ability to work efficiently and resolve customer issues using the most cost effective solution. etc. | 8/11/2020 |
| 847 | Beckman Coulter Diagnostics Louisville, KY Field Service Engineer-Louisville, KY AS/BS Exp: 1-3+ year(s) |
Beckman Coulter Diagnostics Field Service Engineers provide excellent customer service to clients while installing and maintaining diagnostic instrumentation and systems in hospital and stand-alone laboratory environments. As a Field Service Engineer (FSE) you will be the face of Beckman Coulter to customers and support them, directly impacting patient health and overall well-being. Would you like to be part of a team providing front line support to hospital laboratories? Are you ambitious and seeking to drive healthcare forward? The Field Service Engineer in this position will: Under minimal supervision, serve as lead to assigned customers; complete troubleshooting, installation, validation, maintenance, and service repair needs on designated equipment. May assist and/or train newer Field Engineers. Provide excellent and efficient service to Beckman Coulter’s customers, along with technical training on products. Repair, maintain, and install product line(s). etc. | 8/11/2020 |
| 848 | Beckman Coulter Diagnostics Brea, CA Systems Engineer II MS in electrical, mechanical, biomedical, or related engineering Exp: 0-2 years |
We are looking for an engineer to be part of our Clinical Diagnostics Chemistry and Immunoassay Instrument R&D group in Brea, CA. This is an exciting product development opportunity where the primary responsibility will be to perform the following Systems Engineering functions. In this role, you will have the responsibility to: Collect appropriate data to define, identify, analyze, correct and prevent potential system failures. Develop test plans and conduct bench and system level testing that cover the expected customer use environment and operation conditions. Analyze and develop system and sub-system requirements and relationships with component specifications. Analyze, summarize, present, and interpret experimental data to formulate conclusions and make recommendations. etc. | 8/11/2020 |
| 849 | Beckman Coulter Diagnostics West Sacramento, CA Customer Technical Specialist - Microbiology AS in microbiology or related Exp: 1-3 year(s) |
Primary Duties and Responsibilities: We are looking for an energetic, dynamic individual to join our team! The ideal candidate will thrive in a fast-paced, high-volume call center environment and whose passion includes the delivery of exceptional, results oriented experiences for our customers and the patients they serve. Handling Customer Calls to facilitate a 7-day Call Center Support Function. You will be expected to rotate holidays and assist in back filling vacation request for your peers. Provide technical resolutions on Hardware, Software, Consumables and LIS related calls from existing customer base through telephone and electronic (i.e. email, fax, remote diagnostics) technology. Possess excellent phone soft skills and communication skills, both verbal and written. Assign calls to field service when unable to resolve over the phone. etc. | 8/11/2020 |
| 850 | Berg Health Framingham, MA Laboratory Operations Specialist I AS/BS Exp: 0-2 years |
Laboratory Operations Specialist I is a dynamic position that supports all lab operations within the OMICS and Bioanalytical Lab teams ensuring a safe work environment, by maintaining a clean, organized lab and facilitating training as necessary. The successful Lab Support Specialist prioritizes duties for continuous and measurable improvement in the lab. Laboratory Operations Specialist will work primarily in our labs and support instrument calibration, PM tracking, scheduling, and consumables inventory. etc. | 8/11/2020 |
| 851 | BGI Montreal, QC Lab Technician BS in microbiology or related Exp: 1-2 year(s) |
The successful candidate will be responsible for developing and executing standard work procedures on a wide range of molecular biology techniques related to Next Generation Sequencing. Major Responsibilities: Execute on and assist in the development of process instructions that ensure accuracy, throughput, and quality. Operate and monitor laboratory automation and instrumentation. Communicate issues and failures as necessary to the appropriate parties. Apply knowledge and experience in specialized areas, with an understanding of the underlying biochemistry. Use that knowledge and understanding to address problems and situations ordinarily encountered in laboratory manufacturing processes. etc. | 8/11/2020 |
| 852 | Bicycle Therapeutics Lexington, MA Research Associate– Immuno-oncology BS/MS Exp: 1-5 year(s) |
The Research Associate, Immuno-oncology will be primarily responsible for the development and execution of essential in vitro and ex vivo assays of systemic and tumor-targeted immune cell agonists to enhance progress of Bicycle’s oncology pipeline. In this role, he or she will be a key player in implementing the in vitro characterization of our immune modulators. ey Responsibilities: The applicant will have a strong scientific background and hands-on laboratory skills in immunology, immuno-oncology and/or translational oncology with experience in immunological assay development and in vitro pharmacology. The successful candidate will work as part of a team and will be responsible for running and interpreting immunological and cell-based assays to characterize Bicycle® immune modulators. etc. | 8/11/2020 |
| 853 | BillionToOne West Menlo Park, CA Laboratory Technician BS in biology or related Exp: 6+ months |
The CLA I is responsible for assisting with the day-to-day operations and equipment maintenance in the Clinical Laboratory. The CLA I will also be responsible for the pre-analytical phase of testing (e.g., specimen receipt, accessioning, and plasma/buffy coat isolation), performing quality assurance procedures, and complying with all local, state, and federal laboratory requirements. Responsibilities: Perform sample accessioning and isolation procedures according to the laboratory’s standard operating procedures; Clean labware, equipment, and benches; Prepare documents for equipment and personnel records; etc. | 8/11/2020 |
| 854 | BillionToOne West Menlo Park, CA Research Associate BS/MS in microbiology, bioengineering, bioinformatics, physics or related Exp: 1-2 year(s) |
Key Responsibilities: Develop sophisticated and robust next-generation sequencing analysis pipelines under the guidance of a Senior Scientist. Work closely with Process Engineers to design process improvement experiments and analyze the resulting data. Perform analysis of clinical bioinformatics data. Assemble and analyze quality metrics from the clinical laboratory. Collaborate with Senior / Principal Scientists and support new scientific insights. etc. | 8/11/2020 |
| 855 | BioAgilytix Durham, NC Business Development Assistant (temporary) BS in biological science, business administration or related Exp: 1+ year(s) |
Essential Responsibilities: Schedules initial teleconferences with relevant prospects for the Business Development team through cold calling and personalized email messaging; uses established contact lists, email templates, and call scripts to send 300+ emails and make 200+ calls per week. Tracks all activities and ensures meetings scheduled are properly inputted into CRM system (Salesforce). Performs administrative support work specific to sales and marketing departments. Other duties as needed. etc. | 8/11/2020 |
| 856 | BioAgilytix Durham, NC Analyst, Business Development BS/BA in business administration, finance, marketing or related Exp: 0-2 years |
The Business Development Analyst will identify, analyze, and interpret trends in complex data sets and complete internal reporting on key sales metrics. He or she will present insights and recommendations in a consultative manner to internal stakeholders. Essential Responsibilities: Maintains schedules and completes routine internal reporting on key sales metrics. Prepares and provides supporting analysis for month-end, quarter-end, and year-end reporting and metrics. Generates sales performance dashboards and reports using SalesForce. etc. | 8/11/2020 |
| 857 | BioAgilytix Boston, MA Analyst BS/MS in molecular biology, biochemistry, immunology or related Exp: 1 year |
Essential Responsibilities: Prepare worksheets with minimal supervision. Prepare plate maps. Serve as lead analyst on sample analysis projects. Troubleshoot assays. Compile/process data (make power export). Prepare summary tables. Peer review raw data. Order reagents. Participate in assay development and validation. Run assays independently. Adhere to provided method/directive. Prepare buffers. Use LIMS system. Participate in sample analysis. Pipetting. etc. | 8/11/2020 |
| 858 | BioAgilytix Durham, NC Analyst BS/MS in molecular biology, biochemistry, immunology or related Exp: 1 year |
Essential Responsibilities: Prepare worksheets with minimal supervision. Prepare plate maps. Serve as lead analyst on sample analysis projects. Troubleshoot assays. Compile/process data (make power export). Prepare summary tables. Peer review raw data. Order reagents. Participate in assay development and validation. Run assays independently. Adhere to provided method/directive. Prepare buffers. Use LIMS system. Participate in sample analysis. Pipetting. etc. | 8/11/2020 |
| 859 | BioAssay Systems Hayward, CA Research Associate - Manufacturing BS in chemistry, biochemistry or biology Exp: 1-2 year(s) |
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. etc. | 8/11/2020 |
| 860 | BioAssay Systems Hayward, CA Research Associate - Assay Development BS in chemistry, biochemistry or biology Exp: 1-2 year(s) |
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. etc. | 8/11/2020 |
| 861 | Biocare Medical Pacheco, CA Associate I, Product Development BS in biology or related Exp: 0-3 years |
The Associate I, Product Development functions with minimal supervision and guidance within the Reagent Research and Development Laboratory. The Associate I conducts product development activities on new and existing products involving Immunohistochemistry (IHC) and in situ hybridization (ISH) procedures within well-defined guidelines. The Associate I keeps abreast of current methodologies and developments within defined areas of research. The Associate I will at times assist other laboratory members or technical staff on research-related activities. etc. | 8/11/2020 |
| 862 | Biocare Medical Pacheco, CA Associate I, Optimization Experience BS/AS in biology or related Exp: 0-5 years |
The Optimization Experience Associate functions with minimal supervision and guidance within the research and development (R&D) laboratory. The Optimization Experience Associate will conduct various R&D activities on new and existing products involving immunohistochemistry (IHC) procedures including, but not limited to, new product designs and optimizations. The Optimization Experience Associate will assist with troubleshooting of reagents and IHC staining, optimization of client menus and any pre-installation tasks needed to ensure client satisfaction. The Optimization Experience Associate is responsible for collecting and organizing relevant data to be used in the distribution to the applicable teams. etc. | 8/11/2020 |
| 863 | Biocare Medical Pacheco, CA Associate Scientist I, Product Development MS Exp: 1-3 year(s) |
The Associate Scientist I, Product Development functions with minimal supervision and guidance within the Reagent Research and Development Laboratory. The Associate Scientist I conducts R&D activities on new and existing products involving Histology and Immunohistochemistry (IHC) procedures within well-defined guidelines. The Associate Scientist I keeps abreast of current methodologies and developments within defined areas of research. The Associate Scientist I participates in research or clinical collaborative projects. The Associate Scientist I will at times assist other laboratory members or technical staff on research-related activities. etc. | 8/11/2020 |
| 864 | Biocare Medical Pacheco, CA Associate I, Product Design BS Exp: 0-3 years |
Assists the activities associated with IVD reagent development under Design Controls. Supports documentation of new product development and sustainability of existing products to ensure accurate and complete Design records. Contributes to the overall Quality Systems compliance of the Reagent R&D group. Essential Duties and Responsibilities: 1. Product Development/Design Control: a. Facilitates product development projects. b. Drafts Design Outputs for review by Manager, Product Design. etc. | 8/11/2020 |
| 865 | Biocare Medical Pacheco, CA Laboratory Assistant BS in a scientific or engineering field Exp: 0-2 years |
Assist with product development testing tasks and manage assigned lab duties. Essential Duties and Responsibilities: Perform general laboratory related job duties as required. Maintain laboratory equipment logs, stocks solutions and lab supplies. Review and execute test protocols for integration test plan of new and sustaining engineering projects. Enter and update defects in defect management database. Assist with assigned testing and documenting results. Follow all company policies and procedures to ensure product integrity and quality control. Maintains good communication within the team and with other groups involved in the project. etc. | 8/11/2020 |
| 866 | Bioclinica Princeton, NJ Auditor I, Medical Imaging AS in a life science, trial or quality maintenance, or computer science Exp: 0-3 years |
Supports all aspects of audits / audit conduct. Plans, conducts, and reports audits according to Bioclinica’s standard operating procedures (SOPs) and electronic document management system (EDMS) processes. Tracks and/or trends audit issues and/or CAPAs until closure. Provides root cause guidance to CAPA owners and/or conducts root cause analysis when assigned. Champions timely management of quality event reports, audit findings, and CAPAs. Follows-up and verifies effectiveness checks. Ability to work with all levels of Bioclinica personnel and external personnel in a professional and organized manner. Identifies and implements process improvements, with a focus on the audit program. Supports all audit/inspection types (e.g. internal, external, vendor, regulatory inspections, registrar {ISO, SOC etc.}) etc. | 8/11/2020 |
| 867 | Bioclinica Princeton, NJ Associate Medical Writer BS in a life or physical science Exp: 1-2+ year(s) |
Performs study start up responsibilities by: Performing new award tasks such as entering new studies into the MedComm database, creating Medical Affairs and Medical Communications study-specific folders, organizing study documents, requesting signed Protocols, entering document costs in the new award spreadsheet, and notifying assigned Project Teams. Performing a concise and thorough review of study Protocols related to imaging requirements, schedules and windows. Creating, modifying and finalizing Site Manuals, associated fillable forms, and labels. Creating, modifying and finalizing Study Start-Up related Compliance Reports (CRs) such as Protocol Amendment Impact Forms (PAIFs), Notes to File (NTFs), Corrections, non-Quality Event Deviation Reports, and Transfers of Obligation (ToO) as required/applicable. etc. | 8/11/2020 |
| 868 | Bioclinica Princeton, NJ Inside Sales Associate BS/BA Exp: 1-3 year(s) |
Support business development efforts. Contact clients directly at an early stage of the sales lifecycle to initiate meetings and support the development of the RFP pipeline for the Sales Directors. Responsible for developing relationships with clients to expand portfolio with new and existing clients in partnership with the Sales Directors. Supports and operationalizes the Sales team by: Reviewing each sales territory with the designated Sales Manager to identify new and existing targets where penetration and contact is required, enabling the expansion of eHealth solutions. Supporting each defined territory in the priority defined with the Sales Directors to prepare and initiate call plans, support email targeting campaigns and deliver thought leadership pieces which help drive new meetings and enable RFP inclusion. etc. | 8/11/2020 |
| 869 | PTC Therapeutics South Plainfield, NJ Research Associate II, Pharmacology MS in biology Exp: 1+ year(s) |
The Research Associate II, Pharmacology is responsible for conducting scientific experiments that contribute to research and drug discovery activities at PTC. This position assists in maintaining multiple mouse colonies, genotyping process, breeding, and conducting behavioral studies The incumbent is also responsible for communicating experimental results to his/her supervisor and the project team. The Research Associate II, Pharmacology supports adherence to all regulatory requirements and company Standard Operating Procedures (SOPs) including as appropriate. Primary duties/responsibilities: Under general guidance, executes experiments and communicates results as part of multi-disciplinary team(s). Applies relevant scientific principles and techniques to research problems. Maintains detailed laboratory notebooks. Maintains knowledge of state-of-the-art principles and techniques. etc. | 8/11/2020 |
| 870 | Biogen Cambridge, MA Associate Scientist II, Technical Development MS in biology, molecular biology, biochemistry or related Exp: 0-3 years |
We are seeking a highly motivated individual with mammalian cell culture experience, a background in molecular or cellular biology, and a strong interest in automation to join our Cell Line Development Team. Our group is focused on generating industry-leading cell lines for clinical and commercial programs. The candidate’s goals will be to engineer highly productive cell lines that enable fast-tracked program timelines that rely upon plasmid construction, transfection, cloning, high-throughput cell culture platforms, and ambr bioreactors. Additionally, the individual will be empowered to explore technology improvements geared toward advancing efficiency, with special consideration given to candidates with experience or passion for working with automation for custom needs as we push to expand throughput, implement novel production cell lines, develop continuous screening and integrate multi-level omics understanding. etc. | 8/11/2020 |
| 871 | Biogen Research Triangle Park, NC Patient Services Coordinator BS/BA Exp: 1-2 year(s) |
The primary role of the Patient Service Coordinator is to facilitate the customer lifecycle by assisting patients, healthcare providers and others with activities related to starting and staying on therapy. Patient base includes both newly diagnosed and existing Alzheimer patients. Daily interactions involve contact via phone not only with patients but also health care providers, Biogen field force representatives, business service partners, nursing services and other internal work groups. The competitive candidates will have an ability to utilize strong interpersonal skills that will allow for the support and education of patients in their disease state, understanding of medical benefits, Biogen product education and the offering of service option explanations. etc. | 8/11/2020 |
| 872 | Biogen Cambridge, MA Engineer I, Pilot Upstream, Gene Therapy BS/MS in bioengineering, biochemical engineering, biochemistry or related Exp: 0-2 years |
The successful candidate will join a team of scientists responsible for the development of scalable cell culture and purification processes used for the clinical and commercial manufacturing of adeno-associated virus (AAV) gene therapy vectors. Success in this position will require the candidate to independently plan and execute projects and experiments across multiple viral vector and precursor production platforms to support pilot-scale material generation runs and to effectively collaborate with different groups within Gene Therapy and Process Development. Candidates must be motivated and innovative with exceptional analytical and communication skills. etc. | 8/11/2020 |
| 873 | Biogen Cambridge, MA Associate Scientist III, Gene Therapy - Formulation and Drug Product Development MS Exp: 0-2 years |
As a member of Biogen’s Gene Therapy Drug Product development team, the candidate will be responsible for providing analytical, formulation and process development support for drug product development programs. Conducting laboratory studies, both in-house and through external contract laboratories is a requirement of the position. Candidate is expected to work collaboratively in a matrix environment with other members of the gene therapy development team. Essential Responsibilities: Execution of formulation and process development study protocols, stability and product characterization studies with adeno-associated viral vectors. Performing analytical characterization of study samples using various biochemical or biophysical methods. etc. | 8/11/2020 |
| 874 | Biogen Cambridge, MA Associate Scientist II/III – Fluid Biomarker Assay Development MS Exp: 1+ year(s) |
The Fluid Biomarkers group (Section of Clinical Sciences) is seeking a creative and collaborative lab-based scientist engaged in targeted proteomics for the detection of proteins and metabolites in different biological matrices (including plasma, serum, CSF, urine, tissues. This role is required to develop and implement clinically robust LC-MS assays to support clinical programs across the Neurology portfolio. The successful candidate will be capable of multitasking and effective planning to consistently meet deadlines. Responsibilities: Targeted protein biomarker assay development using state of the art liquid-chromatography-mass spectrometry (LC-MS) platforms including nano-LC, orbitrap (Q-Exactive, Q-Exactive +, Q-Exactive HF/HFX, Fusion) and UPLC-QQQ MS (AB Sciex). Sample preparation (tissues and cell lysates) for protein quantification. Biotinylation and various bead-antibody conjugation techniques. etc. | 8/11/2020 |
| 875 | Biogen Cambridge, MA Associate Scientist II, Gene Therapy - Cell Line Technology BS in biology Exp: 1 year |
The successful candidate will work efficiently with team members and independently to plan, conduct, analyze, and document experiments to drive innovation in a cutting-edge modality. Qualifications: Team player with ability to execute tasks independently. Skilled molecular biologist (cloning, PCR, plasmid generation). Experience with mammalian cell culture (aseptic technique, proficiency with suspension cell culture, and experience with high-throughput cell culture desired). Proven track record of successfully planning, executing, and troubleshooting projects and experiments. Demonstration of strong organizational skills. Excellent written and verbal communication skills. etc. | 8/11/2020 |
| 876 | Biogen Research Triangle Park, NC Mechanic II, Maintenance (Drug Product Facility) BS/BA Exp: 1 year |
Major Responsibilities Include: Collaborate with Responsible Engineers and Manufacturing personnel to troubleshoot equipment problems. Provide customer-oriented service and support in a fast-paced manufacturing environment. Sterile Filling equipment Isolators, Cartoner, labeling, Ink Jet Printers Automatic Vial Inspection equipment. Suggest practical changes or improvements to equipment and department work practices. Complete all assigned corrective work orders and Preventative Maintenance work with attention to detail and maintaining required GMP documentation. Follow Standard Operating Procedures in performance of assigned duties. Support manufacturing operations 12/7. etc. | 8/11/2020 |
| 877 | Gyroscope King of Prussia, PA IT Technical Support Engineer BS/BA Exp: Epxerience in Windows 10/MAC oerations |
Help with triaging and setting up hardware (Laptops, printers, Lab systems) and supporting software including Office365, Okta and other platforms we use. We’ll need you to be the lead person to work with third party service providers to ensure end to end support is maintained for our office and remote stall working from home. | 8/9/2020 |
| 878 | Halozyme San Diego, CA Staff Accountant 1, Accounts Payable Bs/BA in accounting or finance Exp: 1 year in accounts payable |
The Staff Accountant 1, Accounts Payable responsibilities include processing a full cycle accounts payable, processing travel and expense reimbursements, month end accruals and reconciling designated general ledger accounts. He/She will interface with multiple departments and personnel from within the organization. | 8/9/2020 |
| 879 | Harpoon Therapeutics South San Francisco, CA Clinical Research Associate BS/BA in sciences or health care discipline Exp: 1-2 years in oncology/orphan drug development |
Maintain and/or accelerate timelines for achieving clinical operational milestones. Serve as the primary liaison with research sites; monitor the day-to-day conduct of the study, and resolve problems associated with the study; provide administrative and logistical support as needed. Ensure that documentation from investigators and investigational sites meets FDA/GCP/ICH requirements | 8/9/2020 |
| 880 | Harvard Bioscience Holliston, MA Manufacturing Engineer BS/BA Exp: 0-2 years in electro-mechanical assemblies |
The qualified candidate will work within a multi-disciplinary team of engineers on DFM, cost reduction, and transfer to production activities. Work closely with assemblers and production leaders to improve manufacturability. Investigate quality issues for engineering improvements. Work closely with operations on design improvement and continuous improvement initiatives. | 8/9/2020 |
| 881 | Helix San Diego, CA Clinical Laboratory Technician - 3rd Shift (CLT) (Temporary) Bs/BA in biological or health sciences Exp: |
We are searching for a highly motivated and team-oriented Clinical Laboratory Technician (CLT) to support a wide variety of molecular biology, biochemical, and extraction techniques to support projects focused on viral infection. Perform specimen processing and accessioning. Perform Automated RNA extraction. Perform PCR-based genetic testing in accordance with standard operating procedures. | 8/9/2020 |
| 882 | Helix San Diego, CA Automations Engineer (Temporary) BS/BA in biological sciences or engineering Exp: 0-2 years |
Support production team by providing on site and immediate diagnostics of liquid handler issues/errors. Provide support for calibration, maintenance, and repair of liquid handling systems. Provide documentation of service, repair or maintenance of liquid handling systems | 8/9/2020 |
| 883 | Helix Bind Boxborough, MA AssEMBLY TECHNICIAN HS Diploma/GED Exp: 0-2 years |
Prior experience not required, however, candidates with familiarity with any industrial assembly and/or machine shop equipment such as saws, drills, electronics soldering, and working with small/miniature machined components, will be given preference. Capable of reading and understanding technical specifications of a mechanical capacity. | 8/9/2020 |
| 884 | Helix Bind Boxborough, MA Mechanical / Biomedical / Instrumentation ENGINEER BS/BA in engineering Exp: 0-5 years |
Identify and analyze design problems to achieve optimal solutions that satisfy cost and technical requirements using both internal and external technical resources. Assemble and test mechanical components for improving instrument functionality. Design test fixtures based on R&D, manufacturing, and quality requirements. | 8/9/2020 |
| 885 | Helix Bind Boxborough, MA Engineering/Service Technician BS/BA, Associates, or Trade certification Exp: 0-2 years in electrical, mechanical installation |
The Engineering Technician will work to maintain, troubleshoot and repair medical diagnostic instruments, commission new equipment, through quality service and professionalism. We are seeking hard working, motivated, and well-organized individuals with a focus on continuous product improvement to exceed expectations. | 8/9/2020 |
| 886 | Helomics Pittsburgh, PA Medical Laboratory Technologist BS in biological sciences Exp: 1+ years in lab |
The technologist is required to maintain and demonstrate cross-functional skills across all areas of the clinical lab. The technologist will be expected to successfully interface cross-departmentally with the Clinical Information Management, Client Services and LIMS groups to ensure the execution of the correct testing for all patients. These interactions will require a thorough knowledge of laboratory/scientific techniques and regulatory requirements including accreditation and governmental regulations. | 8/9/2020 |
| 887 | Hemacare Northridge, MA Research Production AssociateI BS/BA in biological sciences Exp: 1 year in general lab experience |
This position isresponsible for the evaluationof humanblood products for manual orautomated cell isolations, product manufacturer,andcell culture.Perform QC testing and create a certificateof analysis(COA)for products manufactured. Record isolation details on a processing worksheet usinggood documentation practices. Operate flow cytometer and basic lab equipment. | 8/9/2020 |
| 888 | Heska Loveland, CO Accounts Receivable Clerk I HS Diploma/GED Exp: 6 months |
Under the direct supervision of the AR Supervisor, the Accounts Receivable Clerk I will answer and responds to incoming customer calls and email requests. This position will regularly assist with making outbound calls to past due accounts as well as invoice processing, filing and sorting monthly statements, as needed. | 8/9/2020 |
| 889 | Hexagon Bio Menlo Park, CA Research Associate, Molecular Biology BS in molecular biology Exp: 1+ year in industry |
As a Research Associate you’ll operate Hexagon's fungal genome discovery and molecular building block synthesis workflows, core parts of Hexagon’s pipeline which allow us to mine environmental samples for novel fungal genomes and retrieve individual biosynthetic genes to study further. You’ll apply and develop your skills running molecular and microbiological production protocols to operate and refine these pipelines using Hexagon’s suite of specialized robotic and software tools. | 8/9/2020 |
| 890 | High Point Clinical Trials Center High Point, NC Research Nurse LPN/RN or diploma in nursing Exp: 1 year in practical nursing |
Assist in conduct of clinical studies. Provides licensed nursing coverage for studies and performs procedures as allowed by training and delegation. Assist in the conduct of clinical studies while providing licensed coverage. Performs all job responsibilities in accordance with standards of Good Clinical Practice (GCP), clinic standard operating procedures (SOP’s), and OSHA guidelines. | 8/9/2020 |
| 891 | High Point Clinical Trials Center High Point, NC Lab Supervisor BS/BA preferred Exp: 1 year in lab |
Applicants should have demonstrated team management skills as well as working knowledge of IATA sample shipment processes, CLIA-waivered laboratory processes, and ability to fully manage external vendors for our clinical trial testing needs. This position ensures the full reconciliation of all specimens submitted to outside client and vendors in a manner fully compliant to Good Clinical Practice under FDA guidelines. | 8/9/2020 |
| 892 | HighRes Biosolutions Beverly, MA Field Service Engineer BS in mechanical/electrical engineering Exp: 1-2 years |
As a Field Service Engineer, you are responsible for commissioning and calibrating laboratory automation devices to meet internal and customer specifications. As a qualified candidate, you will have mechanical debugging skills, knowledge of machine components, and a basic understanding of liquid handling software. Experience servicing and performing QC on automated liquid handlers is required. You’ll work closely with software and electrical engineers to commission, perform QC and trouble shoot instrumentation in the field. This position will involve travel to customer sites when needed. | 8/9/2020 |
| 893 | Hitachi Chemical Advanced Allendale, NJ QC Microbiology Associate I BS/BA in sciences Exp: 0-1 years in environmental monitoring |
The Quality Control Microbiology Associate I serves as a support role to clinical and commercial production The QC Microbiology Associate will assist environmental monitoring activities to ensure that quality standards are upheld for all products produced at the facility. | 8/9/2020 |
| 894 | Homology Medicines Bedford, MA Research Associate - Molecular Analytical Development (6 Month Contract) MS in biological sciences Exp: 0-4 years |
The individual in this role will be a talented and motivated technician who will focus on the analysis of research/development-grade vector samples using multiple AAV-specific analytical methods. This is a largely laboratory-based position with a focus on providing analytical support for characterizing research-grade vectors. | 8/9/2020 |
| 895 | Homology Medicines Bedford, MA Research Associate, Upstream Development - Pilot Plant Bs or MS in biological/chemical engineering or sciences Exp: 0-3 years |
The individual in this role will be highly motivated, enthusiastic and brings rigor and a desire to deliver on tasks with focus on the development and scale up of cell-based methods for producing AAV vectors. We seek candidates with proven ability to work independently after initial training and collaboratively to achieve optimized project plans, with the goal to deliver products that transform the lives of patients. | 8/9/2020 |
| 896 | HotSpot Monmouth Junction, NJ Associate Biologist, DNA-Encoded Library Group BS or MS in biochemistry or related Exp: 0-4 years |
Characterize protein stability and function. Quantitate and characterize DNA. Perform DEL selections. Evaluate DEL hits. Use SOPs, protocols, and other documentation | 8/9/2020 |
| 897 | Hovone Hovione, NJ Process Engineer BS in chemical science or engineering Exp: 1-3 years in industrial operations |
At Hovione, a Process Engineer's job mission is to ensure the best process engineering knowledge is applied in scaling up chemical and spray drying projects to maximize customer satisfaction ad Hovione's interests and in compliance with all Federal, State, Local and internal policies. It also includes the development of process engineering technical skills to increase the knowledge and offering on the best and state of the art technologies used in the industry. | 8/9/2020 |
| 898 | HTG Tucson, AZ Helpdesk Technican Working towards degree in comp sci or IT Exp: 1+ years |
The Helpdesk Technician’s primary responsibility is to manage all daily operations of the Helpdesk, including but not limited to troubleshooting and resolving inbound tickets, collecting additional information, documenting steps taken, and escalating to other Information Technology team members. The Helpdesk Technician will be challenged to research new issues and increase working knowledge of IT systems through on the job training and mentorship. | 8/9/2020 |
| 899 | Hemosconics Durham, NC Cartridge Automation Technician BS/BA Exp: 1 year in regulated manufacturing environment |
Setup and Shutdown of all equipment associated with the automation line per applicable Work Instruction. Operation of automation equipment in a controlled manufacturing environment. Completion of batch-related documentation in a timely manner and in accordance with regulatory requirements. | 8/9/2020 |
| 900 | Harpoon Therapeutics South San Francisco, CA Clinical Trial Assistant BS/BA in biological sciences Exp: 1 year in clinical research |
Maintain and/or accelerate timelines for achieving clinical operational milestones. File, track and maintain study activity. Manage and ensure the paper and electronic Trial Master File (eTMF) meets FDA/ICH/GCP requirements. Coordinate execution of Non-Disclosure and Confidentiality Agreements (NDAs and CDAs) with study sit | 8/9/2020 |
| 901 | Harpoon Therapeutics South San Francisco, CA Research Associate, Protein Expression BS/BA or MS in biological sciences Exp: BS: 1-5 years, MS: 1-3 years |
Stable and transient transfections of mammalian cell lines. Cryopreservation of cell lines and clarification of conditioned medium. SDS-PAGE, Octet BLI, and Western blot analysis of purified proteins. Materials management and inventory database maintenance. Maintenance of electronic lab notebook and databases, preparation of reports, and regular presentations to summarize results and update management | 8/9/2020 |
| 902 | Bachem Torrance, CA Analytical Scientist - Method Development & Validation MS in analytical chemistry or related Exp: 1+ year(s) |
The Analytical Scientist will fulfill a critical role in GMP operations. This individual helps with the execution of feasibility evaluation of analytical methods, method development and validations, writing of validation protocols, reports and other technical quality documents; conducts validation related investigations and contributes to improvements in laboratory operations. Your Tasks: Independently plan and execute validation studies for test methods. Implement and perform analytical method transfer to Quality Control Department. Write validation protocols and final reports, test methods, standard operating procedures, and technical reports. Under minimal supervision, conduct and document investigations related to validation activities. etc. | 8/5/2020 |
| 903 | Bachem Torrance, CA QA Specialist I (Document Control) BS in science or related Exp: 1+ year(s) |
The Quality Assurance Specialist I (Document Control) fulfills a critical role for Quality Assurance. The primary function of this individual will support all activities related to the Document Control function, including the review and release of SOPs, Forms, Specifications, Batch Records, Plans, Protocols, Reports, etc. through Master Control. This individual will support record management ensuring that the site stays in compliance with FDA and international regulatory requirements. Your Tasks: Review and process all submitted documents through Master Control System in a timely manner, meeting monthly, quarterly and annually department goals. Issue logbooks, active and retired documents as required to meet department goals. etc. | 8/5/2020 |
| 904 | Bachem Vista, CA Chemist I BS in chemistry or related Exp: 1-3 year(s) |
The Chemist (Chem1) function is to develop the peptide manufacture process, manufacture GMP material and perform related activities at Bachem. Your Tasks: Perform synthesis process including solution phase and solid phase peptide synthesis, peptide resin cleavage, resin cleavage with HF or other chemical cocktails. Perform purification process by chromatography, crystallization and other techniques, and in-process test method. Follow approved GMP manufacture directions such as Master Batch Records, Standard Operation Procedures, Standard Test Procedures and other procedures to manufacture GMP materials, perform in-process test, package the product including other related activities. etc. | 8/5/2020 |
| 905 | Bachem Torrance, CA Production Chemist I BS in chemistry or related Exp: 1-3 year(s) |
The Chemist (Chem1) function is to develop the peptide manufacture process, manufacture GMP material and perform related activities at Bachem. Your Tasks: Perform synthesis process including solution phase and solid phase peptide synthesis, peptide resin cleavage, resin cleavage with HF or other chemical cocktails. Perform purification process by chromatography, crystallization and other techniques, and in-process test method. Follow approved GMP manufacture directions such as Master Batch Records, Standard Operation Procedures, Standard Test Procedures and other procedures to manufacture GMP materials, perform in-process test, package the product including other related activities. etc. | 8/5/2020 |
| 906 | Bachem Torrance, CA Production Technician AS in chemistry or related science Exp: 0-2 years |
The Production Technician I performs an integral role as part of the Production team at Bachem. This role is responsible for contributing to the safe and economic manufacture of active pharmaceutical ingredient (API) products, such as peptide or related bioorganic compounds, as a member of a production team. As a Production Technician I, you will be producing APIs from gram to multiple kg scale. The majority of responsibilities will include routine synthetic organic synthesis, the operation of manufacturing equipment and keeping track of batch documentation according to cGMP regulations. etc. | 8/5/2020 |
| 907 | BardyDx New Jersey, NJ Holter Analysis Technician HS diploma/AS/AA Exp: 1-3 year(s) |
Currently, we are looking for Holter Analysis Technicians to join our Clinical Services Team who are passionate about cardiac rhythms and helping cardiac patients through our innovative remote patient monitoring body sensor technologies. The right individuals will join a dynamic and fast-paced start-up environment. Ideal candidates will have CCT or CRAT certification or specialize in cardiac rhythm recognition and interpretation skills. Experience with cardiology or electrophysiology can be advantageous. This position requires PC proficiency, excellent written and verbal communication skills, and meticulous attention to detail. etc. | 8/5/2020 |
| 908 | Baxter Opelika, AL Quality Lab Tech I BS in chemistry or biological sciences Exp: 0-2 years |
Performs required tests in the performance, microbiological, and chemical labs on finished dialyzers and raw materials to support product acceptance. This includes performing analyses, calibrations and maintenance on multiple lab equipment/instruments and entering results in MES. May assist with environmental and process media monitoring by taking samples and testing as required by defined procedure. Maintains cleanliness of labs and lab instruments. Analyze issues on out of specification (OOS) conditions and unusual trends and immediately initiate NCR or deviation and notify Lab Supervisor/Quality Engineer and/or QRM Manager. Orders and maintains lab supply stock (reagents, chemicals, standards etc.) to maximize efficiency. etc. | 8/5/2020 |
| 909 | Baxter Round Lake, IL Research Associate I BS Exp: 1-3 year(s) |
Essential Duties and Responsibilities: Perform microbiology testing in support of medical device and pharmaceutical projects. Record data and assist in the preparation of documentation using Good Documentation Practices (GDP). Support the maintenance of microbiological laboratories and equipment. Understand and apply applicable corporate and divisional Standard Operating Procedures (SOP). Under direction, conduct routine research and/or developmental activities. Plan details of assigned tasks within specific parameters. etc. | 8/5/2020 |
| 910 | Baxter Alliston, ON Associate I, Quality Operations BS in microbiology, chemistry, biological sciences, or engineering Exp: 1-3 year(s) |
Responsible for maintaining Quality and Compliance by ensuring product and manufacturing operations conform to Specification, Standard Operating Procedures and Regulatory Standards (Health Canada & FDA). ESSENTIAL DUTIES AND RESPONSIBILITIES: Provide front line day to day support on product quality issues to ensure GMP, regulatory and procedural compliance to maintain high standards of quality. Support the day shift, with requirement to support plant overtime and planned shutdowns when applicable. Provide technical support on product quality issues. Partner with Quality and Production personnel to ensure mitigating actions are identified and implemented. Support timely follow-up on quality exceptions and their preventative/corrective actions. etc. | 8/5/2020 |
| 911 | Baxter Alliston, ON Associate I, Quality Operations - Nights BS in microbiology, chemistry, biological sciences, or engineering Exp: 1-3 year(s) |
Responsible for maintaining Quality and Compliance by ensuring product and manufacturing operations conform to Specification, Standard Operating Procedures and Regulatory Standards (Health Canada & FDA). ESSENTIAL DUTIES AND RESPONSIBILITIES: Provide front line day to day support on product quality issues to ensure GMP, regulatory and procedural compliance to maintain high standards of quality. Support the day shift, with requirement to support plant overtime and planned shutdowns when applicable. Provide technical support on product quality issues. Partner with Quality and Production personnel to ensure mitigating actions are identified and implemented. Support timely follow-up on quality exceptions and their preventative/corrective actions. etc. | 8/5/2020 |
| 912 | Baxter Alliston, ON Associate I, Quality Operations - Weekend Days BS in microbiology, chemistry, biological sciences, or engineering Exp: 1-3 year(s) |
Responsible for maintaining Quality and Compliance by ensuring product and manufacturing operations conform to Specification, Standard Operating Procedures and Regulatory Standards (Health Canada & FDA). ESSENTIAL DUTIES AND RESPONSIBILITIES: Provide front line day to day support on product quality issues to ensure GMP, regulatory and procedural compliance to maintain high standards of quality. Support the day shift, with requirement to support plant overtime and planned shutdowns when applicable. Provide technical support on product quality issues. Partner with Quality and Production personnel to ensure mitigating actions are identified and implemented. Support timely follow-up on quality exceptions and their preventative/corrective actions. etc. | 8/5/2020 |
| 913 | Baxter Alliston, ON Associate I, Quality Operations - Weekend Night BS in microbiology, chemistry, biological sciences, or engineering Exp: 1-3 year(s) |
Responsible for maintaining Quality and Compliance by ensuring product and manufacturing operations conform to Specification, Standard Operating Procedures and Regulatory Standards (Health Canada & FDA). ESSENTIAL DUTIES AND RESPONSIBILITIES: Provide front line day to day support on product quality issues to ensure GMP, regulatory and procedural compliance to maintain high standards of quality. Support the day shift, with requirement to support plant overtime and planned shutdowns when applicable. Provide technical support on product quality issues. Partner with Quality and Production personnel to ensure mitigating actions are identified and implemented. Support timely follow-up on quality exceptions and their preventative/corrective actions. etc. | 8/5/2020 |
| 914 | Arthrex Naples, FL Engineering Tech - Sutures AS/BS Exp: Not necessary for AS/BS candidates |
Responsible for supporting the Engineering department by assisting engineers with the lifecycle development of medical devices, including new product development and maintenance of released products. Essential Duties and Responsibilities: Generate and maintain mechanical models and drawings utilizing computer aided design (CAD) program, according to specifications determined by the engineer. Assist in the testing of design prototypes and support R&D testing activities of assigned products as assigned. Support design changes to develop and improve products as well as facilitate manufacturing operations. Support QA, Manufacturing, Regulatory, Marketing, Suppliers, and Product Management as assigned. Assist with various aspects of the engineering product development process as assigned. etc. | 8/4/2020 |
| 915 | Arthrex Ave Maria, FL Clean Room Assembler HS diploma or equivalent Exp: 6+ months |
Main Objective: To assemble, label and package medical devices. Essential Duties and Responsibilities: Performs manual and fixture assisted device assembly and packaging on medical device components, kits, convenience packs and / or any clean room specific device assembly as assigned. Performs placement of components onto the blister trays and die cut restraints. Performs label application onto packaging constructs. Performs supplemental label application, blister loading, pouch and blister sealing and visual seal inspection. Load and orient unit devices into unit packages and / or automated equipment. etc. | 8/4/2020 |
| 916 | Arthrex Sandy Springs, SC QC Inspector II - Night Shift HS diploma or equivalent Exp: 1 year |
Performs a variety of quality control test and inspection functions on materials, components and finished goods at various stages of the production process and compiles and evaluates statistical data to determine and maintain quality and reliability of products. Essential Duties and Responsibilities: Performs and documents dimensional inspections on inventory parts using engineering prints, Inspection procedures or work instructions. Selects products for tests at specified stages in production process, and tests products for variety of qualities, such as dimensions, performance, and mechanical, electrical, or chemical characteristics. Records test data, applying statistical quality control procedures. May perform, as needed, nondestructive tests on materials, parts, or products to measure performance, life, or material characteristics. etc. | 8/4/2020 |
| 917 | Ascent Pharmaceuticals Central Islip, NY Quality Control Chemist MS in pharmacy or chemistry Exp: 1 year |
Ascent seeks Quality Control Chemist in Central Islip, NY to scientifically analyze and test raw materials, in-process and finished product samples using modern quality control techniques; develop, validate and test analytical methods for analytical pharmaceutical ingredients (API) and dosage forms; perform quality control/development activities using Chromatography, Spectroscopy, HPLC, GC, TLC, Dissolution etc.; work with advanced analytical equipment like HPLC, GC, DSC and IR and apply knowledge of broad variety of quality control and analytical techniques; validate and analyze results as per regulatory standards such as USP, BP, EP, ICH and USFDA; develop, implement and maintain QC systems and activities; perform in-process inspection, document results and perform a wide variety of inspections, checks, tests and sampling procedures for the manufacturing process; etc. | 8/4/2020 |
| 918 | Assembly Bio Groton, CT Research Associate I / II, Drug Substance Process Development (Microbiome) BS/MS in a life science Exp: 0-2+ years |
The Research Associate I / II, Drug Substance Process Development (Microbiome) will serve as a key team member in the development and qualification of robust processes for production of human commensal bacteria suitable for use as therapeutic agents. The individual will participate in the design, independent execution of experiments and perform data analysis relating to cell banking, fermentation, harvest, and freeze-drying processes. Execution of analytical testing to support rapid data generation would be desirable. It is expected that the individual will work closely with Research, Drug Product Development, Manufacturing, Analytical Development, Quality Control, and Quality Assurance to ensure timely delivery against team and corporate objectives. (S)he will play an important role in the transfer of formulations and processes as well as facilitating phase-appropriate scale-up operations. etc. | 8/4/2020 |
| 919 | Astella South San Francisco, CA Research Associate II, Cell Biology MS Exp: 0-2 years |
The primary purpose of the Research Associate II is to support all cell biology and assay development needs. This position will work primarily in a laboratory setting with Scientist and R&D teams. Essential Job Responsibilities: Culturing of both established cell lines and primary (e.g. human T cells) cell cultures. Generation and quality control assessment of lentivirus to support R&D work. DNA purification to support lentiviral production; additional molecular biology experience (e.g. PCRs, molecular cloning) a plus. etc. | 8/4/2020 |
| 920 | Astella South San Francisco, CA Research Associate II, Protein Purification MS Exp: 0-2 years |
The primary purpose of this role is to support all protein production, purification, and quality control assay needs. This position will work primarily in a laboratory setting with Scientist and R&D teams. If candidate skillset is extended to operational sufficiency with Akta chromatography and Octet kinetic analysis systems then would qualify for Sr. Research Associate role. Essential Job Responsibilities: Culturing and maintenance of established cell lines; transfection of DNA into cell lines for target protein expression. Demonstrated competency with standard protein purification strategies (e.g. protein A, Ni-NTA purification, on-column protease cleavage strategies). etc. | 8/4/2020 |
| 921 | Astella Seattle, WA Research Associate II, Analytics MS Exp: 0-2 years |
The primary purpose of Research Associates working in Analytics (RA II and Senior RA) for our Core Technologies Department is to support the molecular engineering of 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. Essential Job Responsibilities: Developing and routinely executing standard analytical assays including genotyping PCR/qPCR and flow cytometry. Performing standard molecular biology techniques including primer design, molecular cloning, and Sanger sequencing. etc. | 8/4/2020 |
| 922 | Astella Seattle, WA Research Associate II, Cell Editing MS Exp: 0-2 years |
Essential Job Responsibilities: Designs and executes AAV-mediated gene-editing of pluripotent stem cells in a controlled manufacturing environment. Performs data collection, analysis and interpretation for stem cell culture and gene-editing processes. Participates in group meetings and regularly presents at cross-functional team meetings. Prepares and reviews the work of others, including but not limited to, technical slide decks, reports, Standard Operating Procedures (SOPs) and production batch records. May serve as a technical resource for preparation of regulatory filings. Supports Process Development to transfer manufacturing processes. etc. | 8/4/2020 |
| 923 | Astella Seattle, WA Research Associate I, Process Development BS Exp: 0-3 years |
Universal Cells carries out clinical-grade AAV-mediated gene-editing of pluripotent stem cells. The Research Associate I Process Development 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. The Research Associate will be formally trained and will perform all fundamental skills including record keeping, general lab skills, equipment use and maintenance, aseptic technique/cell culture, and basic troubleshooting. They will assist with projects and lead day-to-day activities based on abilities. They will keep appropriate documentation, including lab notebooks, batch documentation and experimental summaries. etc. | 8/4/2020 |
| 924 | Astella Seattle, WA Research Associate II, Core Technologies MS Exp: 0-2 years |
The primary purpose of Research Associates working (RA II and Senior RA) for our Core Technologies Department is to support the molecular engineering of our gene edited Universal Donor Cells. They will work as a key team member on a fast-paced team to assist with Adeno-Associated Virus production and the development and execution of molecular assays to characterize our proprietary gene edited cells. Essential Job Responsibilities: Performing plasmid DNA isolation and producing Adeno-Associate Virus under controlled conditions following SOPs and with detailed real-time documentation. Routinely performing standard molecular biology techniques including primer design, molecular cloning, gDNA isolation, PCR, and Sanger sequence analysis. etc. | 8/4/2020 |
| 925 | AstraZeneca Gaithersburg, MD R&D Associate I/II - Purification Process Sciences BS/MS in biochemistry or chemical engineering or related Exp: 0-2+ years |
The successful candidate will: Develop and characterize downstream processes for the manufacture of biopharmaceuticals (monoclonal antibodies and other proteins) in late stage clinical development through commercial launch. Be responsible for a portion of a purification development project. Make observations, analyze data and interpret results. Maintain accurate records of experimental results, review, analysis, and interpretation of experimental data. Make periodic presentations in group meetings, project team meetings, and in one-on-one situations. Prepare/review development reports, tech transfer and process validation documents, regulatory submissions. etc. | 8/4/2020 |
| 926 | Atreca South San Francisco, CA Research Associate or Senior Research Associate, Protein Engineering MS in cell biology, molecular biology, immunology or bioengineering Exp: Not necessary for MS candidates |
We are seeking a motivated and enthusiastic Research Associate or Sr Research Associate to join our Protein Engineering group. The successful candidate will play a key role in further developing our yeast display platform and applying it to engineer antibodies and bispecifics. Duties & Responsibilities: Culture yeast and perform flow cytometry assays. Sort libraries by FACS and help with NGS sample preparations (plasmid prep and PCR). Help develop methods for selecting yeast-displayed antibodies bound to cancer cells. Follow laboratory safety guidelines and practices. etc. | 8/4/2020 |
| 927 | Atum Newak, CA Mammalian Tissue Culture Associate BS in cell biology Exp: 1+ year(s) |
This an entry-level position within our protein group. The ideal candidate will be responsible for maintenance of mammalian cell culture stocks, transfection of cell cultures expressing a variety of protein types including therapeutic proteins, antigens and assay reagents. They will not be satisfied with just doing their part but being part of a collaborative team that aims to continually improve. Responsibilities of the position: Tissue Culture: Maintain various mammalian cell lines using sterile techniques; transiently transfect cell cultures for the generation of recombinant proteins; determine cell counts and cell viability using microscope and automated cell counting devices. Monitor metabolites and macromolecular products and take endpoint measurements that could include western blotting an titer measurement using ForteBio Octet. etc. | 8/4/2020 |
| 928 | Atum Newak, CA Protein Purification Associate (Mammalian) BS in biology or related Exp: 1-3 year(s) |
This an entry-level position within our mammalian protein purification group. The ideal candidate will be responsible for purification and characterization of a variety of protein types including therapeutic proteins, antigens and assay reagents expressed in mammalian cells. They will not be satisfied with just doing their part, but will thrive on being part of a collaborative team that aims to continually improve. Proteins will be purified at various scales ranging from high throughput robotic purification to many grams. Additionally, the incumbent will have opportunities to learn cell culture, bacterial and yeast fermentation in addition to bioanalytical techniques. etc. | 8/4/2020 |
| 929 | Boston Scientific Arden Hills, MN Quality Engineer I BS Exp: 0-2 years |
The Quality Engineer I will provide Quality/Process Engineering support to the Cardiac Rhythm Management and Neuromodulation and potentially other businesses to ensure delivery of the highest quality product to the customer. They will partner with manufacturing and operations to provide quality engineering support and the highest quality of our products. This position may also provide quality engineering support to additional manufacturing lines as necessary. Your Responsibilities Will Include: Reduces and controls process defects (scrap, nonconforming material, customer complaints) by leading efforts and cross-functional teams focused on identifying the primary root causes and implementing corrective and preventative actions. May be responsible for implementing product stops & documenting release criteria. Develops and implements product quality plans, documents and systems by creating product specifications, quality specifications, quality plans, risk analysis, FMEAs in conjunction with other product development team members. May be responsible for risk analyses and FMEAs. etc. | 8/4/2020 |
| 930 | Boston Scientific Arden Hills, MN Manufacturing Technician III (1st Shift) AA Exp: 1-3 year(s) |
With general supervisory direction, you will be responsible for performing support functions for manufacturing operations, including troubleshooting equipment and process issues, and performing and documenting machine maintenance procedures. Additionally, it is expected that you will partner with engineering in developing methods and procedures to control or modify manufacturing processes. Your Responsibilities Will Include: Identify and troubleshoot process, material or equipment problems to minimize down time. Perform preventative maintenance and calibration procedures, as well as author equipment maintenance and calibration procedures. Modify existing and develop new tooling and fixtures. Revise existing documents, processes, and/or methods to correct or improve processes/product. etc. | 8/4/2020 |
| 931 | Boston Scientific Maple Grove, MN Machine Operator I - 3rd Shift - Maple Grove--Grinding HS diploma/AS/AA Exp: 1 year |
Your Responsibilities Include: Understands and adheres to safety policies and practices. Responsible for quality and adheres to manufacturing process requirements, the Boston Scientific Corporation Quality Policy and the Strategic Quality Process (SQP). Builds product by following all processes in which certified (in their most current revision), and completes other assigned work, while meeting manufacturing goals a8nd metrics. Gains basic understanding of Lean Manufacturing and related principles. Willing to flex and rotate as necessary and work well with all group members, both within the team and cross-functionally. Under the direction of other maintains accurate records such as Manufacturing Execution System (MES), Shop Floor Paperwork (SFP), training Records System (TRS), Product Data Management (PDM), Systems Application & Products (SAP) and Process Equipment Optimization (PEO). etc. | 8/4/2020 |
| 932 | Boston Scientific Maple Grove, MN Machine Operator I - 1st Shift - Maple Grove--Grinding HS diploma/AS/AA Exp: 1 year |
Your Responsibilities Include: Understands and adheres to safety policies and practices. Responsible for quality and adheres to manufacturing process requirements, the Boston Scientific Corporation Quality Policy and the Strategic Quality Process (SQP). Builds product by following all processes in which certified (in their most current revision), and completes other assigned work, while meeting manufacturing goals a8nd metrics. Gains basic understanding of Lean Manufacturing and related principles. Willing to flex and rotate as necessary and work well with all group members, both within the team and cross-functionally. Under the direction of other maintains accurate records such as Manufacturing Execution System (MES), Shop Floor Paperwork (SFP), training Records System (TRS), Product Data Management (PDM), Systems Application & Products (SAP) and Process Equipment Optimization (PEO). etc. | 8/4/2020 |
| 933 | Boston Scientific Maple Grove, MN Manufacturing Technician I (3rd Shift) AA Exp: 0-1 year(s) |
With general supervisory direction, you will be responsible for performing support functions for manufacturing operations, including troubleshooting equipment and process issues, and performing and documenting machine maintenance procedures. Additionally, it is expected that you will partner with engineering in developing methods and procedures to control or modify manufacturing processes. Your Responsibilities Will Include: Identify and troubleshoot process, material or equipment problems to minimize down time. Execute validation plans and compile data. Collect data and perform basic statistical analysis for process characterization and scrap reduction goals. etc. | 8/4/2020 |
| 934 | Boston Scientific Arden Hills, MN Manufacturing Technician I (3rd Shift) AA Exp: 0-1 year(s) |
With general supervisory direction, you will be responsible for performing support functions for manufacturing operations, including troubleshooting equipment and process issues, and performing and documenting machine maintenance procedures. Additionally, it is expected that you will partner with engineering in developing methods and procedures to control or modify manufacturing processes. Your Responsibilities Will Include: Identify and troubleshoot process, material or equipment problems to minimize down time. Execute validation plans and compile data. Collect data and perform basic statistical analysis for process characterization and scrap reduction goals. etc. | 8/4/2020 |
| 935 | Boston Scientific Maple Grove, MN Machine Operator I - 2nd Shift - Maple Grove--Grinding Job HS diploma/AS/AA Exp: 1 year |
Your Responsibilities Include: Understands and adheres to safety policies and practices. Responsible for quality and adheres to manufacturing process requirements, the Boston Scientific Corporation Quality Policy and the Strategic Quality Process (SQP). Builds product by following all processes in which certified (in their most current revision), and completes other assigned work, while meeting manufacturing goals a8nd metrics. Gains basic understanding of Lean Manufacturing and related principles. Willing to flex and rotate as necessary and work well with all group members, both within the team and cross-functionally. Under the direction of other maintains accurate records such as Manufacturing Execution System (MES), Shop Floor Paperwork (SFP), training Records System (TRS), Product Data Management (PDM), Systems Application & Products (SAP) and Process Equipment Optimization (PEO). etc. | 8/4/2020 |
| 936 | Avion Pharmaceuticals Wichita Falls, TX Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Rheumatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 8/4/2020 |
| 937 | Avion Pharmaceuticals Tallahassee, FL Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Rheumatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 8/4/2020 |
| 938 | Avion Pharmaceuticals Lynchburg, VA Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Rheumatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 8/4/2020 |
| 939 | Avion Pharmaceuticals Cherry Hill, NJ Pharmaceutical Sales Representative BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Rheumatology, and related specialties. The primary call point will be OB-GYN’ & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 8/4/2020 |
| 940 | Avion Pharmaceuticals Alphretta, GA Inside Sales Representative AS/AA/BS/BA Exp: 1 year |
The Inside Sales Representative/ Customer Service Associate will assist the Sales & Marketing function by building a rapport and strong relationships that are necessary to increase sales and product placement for Avion's product portfolio. We are looking for a positive and motivated individual who would be passionate about our company and product portfolio. The ideal candidate will also have excellent customer service, communication, and organizational skills. ESSENTIAL DUTIES AND RESPONSIBILITIES: Initiate introductory calls with the objective of developing a long-term business relationship with customer accounts (70% doctors and 30% pharmacies). Build, sustain & maximize customer relationships through timely routine contact with new and existing customers. etc. | 8/4/2020 |
| 941 | Assembly Bio Groton, CT Contract Lab Technician I/II (Microbiome) AS/AA Exp: 0-2 years |
The Laboratory Technician I or II, Drug Substance Process Development (Microbiome) will provide support functions in the development and qualification of robust processes for production of human commensal bacteria suitable for use as therapeutic agents. The individual will assist laboratory operations by preparing media, equipment, and executing housekeeping duties such as autoclaving, according to written procedures. Documentation of these duties in laboratory notebook systems is expected. Key Responsibilities include: Follow written procedures for consistent and reliable preparation of complex media recipes. Documentation in laboratory notebook systems. etc. | 8/4/2020 |
| 942 | Greenlight Biosciences Research Triangle Park, NC Research Associate – Plant Biology (Contract Position) BS in biology Exp: 1-2 years |
Collaboratively design and conduct plant phenotyping assays to determine treatment efficacy. Conduct molecular analyses of gene expression using PCR and RT-qPCR. Sow and maintain plants under a variety of conditions in chamber and greenhouse settings | 8/2/2020 |
| 943 | Greenlight Biosciences Medford, MA Research Associate / Sr. Research Associate – Molecular Biology BS or MS in chemical/biological engineering or sciences Exp: 1-2 years in biotech/pharma |
he successful candidate will support ongoing high-throughput platform production and optimization in the context of several milestone-driven projects. Plan & perform routine molecular biology techniques such as PCR, DNA subcloning, in vitro transcription, cell transformation, cell culture, protein expression & purification, nucleic acid isolation as well as more advanced methods in support of research projects | 8/2/2020 |
| 944 | Greenlight Biosciences Medford, MA Research Associate / Sr. Research Associate – Molecular Biology BS or MS in engineering or biological sciences Exp: 1-2 years in biotech/pharma |
Plan & perform routine molecular biology techniques such as PCR, DNA subcloning, in vitro transcription, cell transformation, cell culture, protein expression & purification, nucleic acid isolation as well as more advanced methods in support of research projects. Execute experiments and associated analytics (such as enzyme assays) at different scales (ranging from 10s of µLs to 10s of Ls) for debottlenecking & optimization and | 8/2/2020 |
| 945 | Grifols Hattiesburg, MS Biomedical Technician HS Diploma/GED Exp: 6-12 montsh as medical assistant or phlebotomy training |
Identify and screen donors by reviewing medical records and logs and evaluate the donor as to suitability. Screening includes asking health related questions and referring to medical staff when necessary; taking vital signs (blood pressure, pulse and temperature), performing fingerstick (HCT & Total Protein), and reviewing results using the applicable donor management system Maintain donor confidentiality at all times in all areas. | 8/2/2020 |
| 946 | Grifols Memphis, TN Laboratory Quality Assurance Coordinators - 2nd Shift BS/BA in biological or chemical sciences Exp: 0-2 years |
This position is responsible for performing quality assurance functions in the laboratory, including the review of test records, reviewing records, monitoring employee practices, assessing activities for compliance to procedures, and keeping management informed of any quality concerns related to the laboratory operator. | 8/2/2020 |
| 947 | Grifols Memphis, TN Laboratory Quality Assurance Coordinators - 1st Shift BS/BA in biological or chemical sciences Exp: 0-2 years |
This position is responsible for performing quality assurance functions in the laboratory, including the review of test records, reviewing records, monitoring employee practices, assessing activities for compliance to procedures, and keeping management informed of any quality concerns related to the laboratory operator. | 8/2/2020 |
| 948 | Grifols Kingsport, TN Biomedical Technician HS Diploma/GED Exp: 6-12 montsh as medical assistant or phlebotomy training |
Provide a positive customer experience by providing health information as per standard operating procedure (SOPs) or as directed by the center Medical staff , explaining fees schedules and bonus programs, instruct donors regarding the importance of plasma donation and explains the uses of the products made from donated plasma. | 8/2/2020 |
| 949 | Grifols Asheville, NC Donor Processor HS Diploma/GED, medical technologist degree preferred Exp: 0-2 years |
This position is responsible for processing a potential plasma donor from their initial registration at the Source Plasma Center through various procedures and tests that are part of the screening to determine if the donor is suitable for plasmapheresis. | 8/2/2020 |
| 950 | Grifols Houston, TN Donor Center Technician HS Diploma/GED Exp: 0-2 yearss, elgible for licensures |
Our ideal Donor Center Technician is a stand out colleague who is patient, can handle multiple tasks, and adapt to a dynamic work environment. Conducts pre-donation medical screening in accordance with established guidelines. You determine Hematocrit (HCT) and Protein via finger stick and use of the hematastat and refractometer. | 8/2/2020 |
| 951 | Grifols Dothan, AL Biomedical Technician HS Diploma/GED Exp: 6-12 montsh as medical assistant or phlebotomy training |
Provide a positive customer experience by providing health information as per standard operating procedure (SOPs) or as directed by the center Medical staff , explaining fees schedules and bonus programs, instruct donors regarding the importance of plasma donation and explains the uses of the products made from donated plasma. | 8/2/2020 |
| 952 | Guardant Redwood City, CA Clinical Research Associate BS in biological sciences or medical speciality Exp: 1-2 years in clinical research |
The Clinical Research Associate l (CRA) is responsible for monitoring activities that will lead to successful execution of IVD clinical studies. They will proactively identify and resolve clinical project issues and participate in process improvement initiatives as applicable. The CRA engages with internal and external stakeholders as a member of the Clinical Trial Operations team. | 8/2/2020 |
| 953 | Guardant Redwood City, CA Clinical Trials Assistant BS in biological related field Exp: 1 year in clinical research or GCP |
The Clinical Trial Assistant (CTA) is primarily responsible for the coordination of activities associated with the setup and management of clinical studies under the direction of, or as delegated by a member of the Clinical Trial team. Responsibilities will range from clinical study coordination to data entry projects and general office work. | 8/2/2020 |
| 954 | Guardant Spring, TX Client Services Associate BS/BA Exp: 1 year in client experience |
CSA is responsible for receiving and responding to all types of communication: phone, email and web inquiries from customers (physician offices, laboratories, and hospitals), sales representatives and patients. Adhering to Standard Operating Procedures (SOP’s) pertaining to data entry and data verification requirements | 8/2/2020 |
| 955 | Gritstone Oncology Cambridge, MA BIOREPOSITORY TECHNICIAN CONTRACTOR (Specimen Management) AS/AA or BS/BA in sciences or healthcare Exp: 1-2 years in lab setting |
The Biorepository Technician Contractor is directly responsible for supporting the manufacturing and research labs under the direction of the Translational Medicine Operations function at Gritstone. The Contractor performs a variety of tasks associated with the tracking, receipt, storage, maintenance and retrieval of biospecimens collected as part of Gritstone’s research programs. | 8/2/2020 |
| 956 | GSK King of Prussia, PA Lead Automation Engineer - Facilities BS/BA in engineering, life sciences, biology Exp: 0-8 years |
Provide technical leadership in support of building & utility control systems and network infrastructure. Critical systems include Emerson DeltaV, Siemens BAS, and Rockwell PLCs. Collaborate with building stakeholders and vendors throughout the automation lifecycle: gather system/end user requirements; complete design, implementation, and testing/validation of changes; maintain documentation; maintain and monitor various site automation systems. | 8/1/2020 |
| 957 | GSK St. Louis , MO Manufacturing Material Handler HS Diploma/GED Exp: 1-5 years in production |
Ensure quality and compliance in accordance with established procedures and standards of the Quality System. Locate finished tablets bins and correctly stage and issue bins as needed to support packaging department. Locate and transport raw materials to floors as needed. Collect, transport, and cleanout empty bins. Support the removal of trash and waste on an as needed basis. Fill blending dump stations as required. Fill preweigh intermediate bulk containers as required. | 8/1/2020 |
| 958 | GSK St. Louis , MO Manufacturing Operator HS Diploma/GED Exp: 1-5 years in production |
Operate and troubleshoot a variety of machinery. Operate the worksaver and standup/sitdown lifts as needed. Utilize manlifts. Perform line changeovers, which include cleaning, disassembly, re-assembly of line equipment and lubrication. Comply with and support the GSK Environmental, Health and Safety policies and procedures. | 8/1/2020 |
| 959 | GSK Lincoln, NE HVAC Technician (2nd Shift) Associates in HVAC technology Exp: 0-3 years |
As a GMP system owner, the HVAC Technician is responsible to maintain a compliant state, troubleshoot, inspect, repair and document work on core facilities equipment or systems that support the manufacture and packaging of over the counter, dietary supplement and medical device products. | 8/1/2020 |
| 960 | GSK Richmond, VA Analytical Associate Scientist BS in chemistry Exp: 0-2 years |
As an Operational QA Staff, you will manage/lead/be responsible for working on the shop floor addressing quality issues during production shift operating hours. Additional responsibilities include supporting incident and deviation investigations, participation in internal auditing activities and batch record review. | 8/1/2020 |
| 961 | Gliknik Baltimore, MD Laboratory Research Associate BS/BA in life sciences Exp: Entry Level |
Responsibilities include: reagent preperation, molecular biology work, experiments with aseptic cell cultures and protein pruification. Other responsibilities include completing appropriate documentation of experiments including laboratory notebooks, equipment logbooks and inventory forms, preparation of technical reports, summaries, protocols and quantitative analyses with minimal supervision. | 8/1/2020 |
| 962 | GBT South San Francisco, CA CONTRACT – RESEARCH ASSOCIATE, PHARMACOLOGY BS in life sciences/engineering Exp: 0-2 years lab experience |
Perform in vivo pharmacology studies with hematological disease models and conduct in vivo drug efficacy studies to support early drug discovery projects. Develop and troubleshoot novel in vivo disease models for mechanism of action studies. Plan, execute, analyze, and document experiments | 8/1/2020 |
| 963 | Globus Medical San Antonio, TX Manufacturing Technician HS Diploma/GED Exp: 1 year in manufacturing |
The Manufacturing Technician is responsible for performing human tissue processing activities in accordance with FDA regulations, AATB Standards and SOPs. Preparing sections of human tissue for surgical implantation. Utilizing special techniques, instrumentation, and equipment to evaluate, cut, shape, grind and package tissue to exacting specifications and protocols | 8/1/2020 |
| 964 | Globus Medical San Antonio, TX Manufacturing Technician HS Diploma/GED Exp: 1 year in manufacturing |
The Manufacturing Technician is responsible for performing human tissue processing activities in accordance with FDA regulations, AATB Standards and SOPs. Preparing sections of human tissue for surgical implantation. Utilizing special techniques, instrumentation, and equipment to evaluate, cut, shape, grind and package tissue to exacting specifications and protocols | 8/1/2020 |
| 965 | Gore Flagstaff, AZ Quality Control Unit Associate College degree Exp: 1 year minimum in manufacturing |
Ensuring appropriate cGMP documentation is generated, revised, approved and maintained. Reviewing associated documentation and labeling for accuracy and completeness. Verifying lot acceptance results for adherence to specification, limits or other acceptance criteria. Approving these results, as required | 8/1/2020 |
| 966 | Grail Menlo Park, CA Research Associate 1/2 BS/BA in biological or chemical sciences Exp: 1-2 years in BSL2 labs |
As a Research Associate in GRAIL’s R&D Group, you will play an integral role in the development of technology and workflows for genomics-based clinical assays. The ideal candidate should be detail-oriented and have experience with blood processing, nucleic acid extraction, and strong molecular biology skills. | 8/1/2020 |
| 967 | Grail Menlo Park, CA Process Engineer 1/2 (Equipment Qualification) BS or MS in biological sciences or engineering Exp: 1-4 years in process engineering/R&D in med/pharma |
Design and characterize new laboratory equipment qualification processes within an NGS setting. Participate in the development of product plans, evaluation of processes and process risk, and development of project timelines. Develop and execute qualification studies for new and existing equipment in accordance with ISO standards. | 8/1/2020 |
| 968 | Grail Menlo Park, CA Core Services Research Associate 1/2 BS in relevant Exp: 1+ years in NGS |
Execute on forecasted R&D experiments ranging from reagent evaluation and qualification to general data generation activities. Execute on automated and manual sample preparation and NGS assays. Be responsible for accurately recording work performed per GLP, including results and methodology. | 8/1/2020 |
| 969 | Grand River Grand Rapids, MI ASEPTIC MANUFACTURING ASSOCIATE 2ND SHIFT HS Diploma/GED Exp: 0-1 years in manufacturing |
Responsible for performing various routine manufacturing tasks following established procedures and cGMP regulations under guidance of a production supervisor and/or senior management. Follow production and manufacturing procedures. Perform equipment preparation, bulk drug formulation, and aseptic filling duties as needed. | 8/1/2020 |
| 970 | Grand River Grand Rapids, MI QC Biochemist I BS/BA in chemistry Exp: 0-3 years in pharma |
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. Perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients, excipients and finished pharmaceutical products. | 8/1/2020 |
| 971 | Grand River Grand Rapids, MI Microbiology Technician BS/Ba in microbiology Exp: 0-2 years |
Supports quality control and assurance by assisting the microbiology department with environmental monitoring, water testing, and client specific testing. Performs sampling of water pure steam to support manufacturing activities. Performs Environmental Monitoring of aseptic filling rooms and supporting areas. | 8/1/2020 |
| 972 | Grand River Grand Rapids, MI Mechanical Engineer BS/BA in engineering or sciences Exp: 1+ years in FDA regulated environment |
Assist the Grand River Aseptic Manufacturing Facilities & Engineering and Operations departments by specializing in facility and utility optimization and providing subject matter expertise on mechanical systems. Run projects and oversee construction activities. Demonstrate, build, and enforce the best practices for all engineering projects and functions within the facilities. | 8/1/2020 |
| 973 | Grand River Grand Rapids, MI ASEPTIC MANUFACTURING ASSOCIATE - 3RD SHIFT HS Diploma/GED Exp: 0-1 years in manufacturing or lab environment |
Responsible for performing various routine manufacturing tasks following established procedures and cGMP regulations under guidance of a production supervisor and/or senior management. Follow production and manufacturing procedures. Perform equipment preparation, bulk drug formulation, and aseptic filling duties as needed. | 8/1/2020 |
| 974 | Globus Medical Audubon, PA Regulatory Associate BS/BA in health or sciences, engineering is a plus Exp: 0-2 years in med devices |
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. | 8/1/2020 |
| 975 | Abbvie Lake County, IL Pharmacy Technician HS diploma/AS/AA Exp: 1+ year(s) |
The Pharmacy Technician position exists to support the pharmacist(s) in completing the duties associated with entering and managing drug therapy orders, fulfilling, and dispensing prescriptions, maintaining pharmacy records and other professional activities. This position is responsible for collaborating with and supporting Pharmacy Leads and Supervisors in day to day activities, issue resolution, and completion of project tasks. Responsibilities: Assist the pharmacist with practice of pharmacy in accordance with federal, state and local regulations, HIPAA guidelines, corporate and departmental policies and procedures. Assist pharmacists in the picking, labeling, packing and shipping of orders; by accurately interpreting healthcare provider’s prescription orders and entering it into the core pharmacy system; etc. | 7/28/2020 |
| 976 | ImmunityBio Louisville, CO Associate, Manufacturing Operations MS Exp: 1-3 year(s) |
The candidate is responsible for supporting manufacturing. All functions and roles of the manufacturing process are required to be performed with adherence to cGMP to ensure successful, quality operations. The candidate will also participate in cross-functional projects with Product Development (PD) and Process Engineering (PE) to develop, scale-up, and transfer new products. DUTIES AND RESPONSIBILITIES: Performs manufacturing activities according to cGMP guidelines, including batch record execution, product and equipment changeover, manufacturing equipment troubleshooting, issue resolution. etc. | 7/28/2020 |
| 977 | ImmunityBio Louisville, CO Associate, Quality Control - Microbiology BS/BA in microbiology Exp: 1-3 year(s) |
The Associate, QC - Microbiology role will perform environmental monitoring, various testing, equipment troubleshooting/maintenance, and may assist with the drafting of SOPs, protocols, and reports to support manufacturing operations. Organizes daily workload and relevant resource requirements in an efficient manner. Important aspects of this role include excellent organization skills, flexibility, and the ability to thrive in a fast-paced, highly interactive, goal-oriented team environment with minimal supervision. etc. | 7/28/2020 |
| 978 | Amarin Chicago, IL Sales Professional- CHICAGO LOOP, IL BS/BA Exp: 1 year |
The company’s U.S. entity, Amarin Pharma Inc., is seeking a Sales Professional for the CHICAGO LOOP, IL territory. The Sales Professional meets established sales goals in promoting Vascepa to general practitioners, specialists and other healthcare professionals in compliance with internal policy and applicable laws/regulations. The Sales Professional will be supported in this initiative with tools and promotional resources designed to have high local impact. The successful professional will achieve sales goals and demonstrate the ability to target and manage their territory strategically while operating within an assigned budget (and adhering to all compliance and administrative duties). etc. | 7/28/2020 |
| 979 | Amarin Tulsa, OK Sales Professional- TULSA, OK BS/BA Exp: 1 year |
The company’s U.S. entity, Amarin Pharma Inc., is seeking a Sales Professional for the TULSA, OK territory. The Sales Professional meets established sales goals in promoting Vascepa to general practitioners, specialists and other healthcare professionals in compliance with internal policy and applicable laws/regulations. The Sales Professional will be supported in this initiative with tools and promotional resources designed to have high local impact. The successful professional will achieve sales goals and demonstrate the ability to target and manage their territory strategically while operating within an assigned budget (and adhering to all compliance and administrative duties). etc. | 7/28/2020 |
| 980 | Amarin Lee Summit, MO Sales Professional- KANSAS CITY E, MO BS/BA Exp: 1 year |
The company’s U.S. entity, Amarin Pharma Inc., is seeking a Sales Professional for the KANSAS CITY E, MO territory. The Sales Professional meets established sales goals in promoting Vascepa to general practitioners, specialists and other healthcare professionals in compliance with internal policy and applicable laws/regulations. The Sales Professional will be supported in this initiative with tools and promotional resources designed to have high local impact. The successful professional will achieve sales goals and demonstrate the ability to target and manage their territory strategically while operating within an assigned budget (and adhering to all compliance and administrative duties). etc. | 7/28/2020 |
| 981 | Amarin Boise, ID Sales Professional- BOISE, ID BS/BA Exp: 1 year |
The company’s U.S. entity, Amarin Pharma Inc., is seeking a Sales Professional for the BOISE, ID territory. The Sales Professional meets established sales goals in promoting Vascepa to general practitioners, specialists and other healthcare professionals in compliance with internal policy and applicable laws/regulations. The Sales Professional will be supported in this initiative with tools and promotional resources designed to have high local impact. The successful professional will achieve sales goals and demonstrate the ability to target and manage their territory strategically while operating within an assigned budget (and adhering to all compliance and administrative duties). etc. | 7/28/2020 |
| 982 | Amarin Tacoma, WA Sales Professional - TACOMA, WA BS/BA Exp: 1 year |
The company’s U.S. entity, Amarin Pharma Inc., is seeking a Sales Professional for the TACOMA, WA territory. The Sales Professional meets established sales goals in promoting Vascepa to general practitioners, specialists and other healthcare professionals in compliance with internal policy and applicable laws/regulations. The Sales Professional will be supported in this initiative with tools and promotional resources designed to have high local impact. The successful professional will achieve sales goals and demonstrate the ability to target and manage their territory strategically while operating within an assigned budget (and adhering to all compliance and administrative duties). etc. | 7/28/2020 |
| 983 | Amarin Sarasota, FL Sales Professional- SARASOTA, FL BS/BA Exp: 1 year |
The company’s U.S. entity, Amarin Pharma Inc., is seeking a Sales Professional for the Sarasota, FL territory. The Sales Professional meets established sales goals in promoting Vascepa to general practitioners, specialists and other healthcare professionals in compliance with internal policy and applicable laws/regulations. The Sales Professional will be supported in this initiative with tools and promotional resources designed to have high local impact. The successful professional will achieve sales goals and demonstrate the ability to target and manage their territory strategically while operating within an assigned budget (and adhering to all compliance and administrative duties). etc. | 7/28/2020 |
| 984 | Amarin Lima, OH Sales Professional-Lima, OH BS/BA Exp: 1 year |
The company’s U.S. entity, Amarin Pharma Inc., is seeking a Sales Professional for the Lima, OH territory. The Sales Professional meets established sales goals in promoting Vascepa to general practitioners, specialists and other healthcare professionals in compliance with internal policy and applicable laws/regulations. The Sales Professional will be supported in this initiative with tools and promotional resources designed to have high local impact. The successful professional will achieve sales goals and demonstrate the ability to target and manage their territory strategically while operating within an assigned budget (and adhering to all compliance and administrative duties). etc. | 7/28/2020 |
| 985 | APi North Augusta, SC Quality Assurance Trainer BS/BA in biology, chemistry or other life science Exp: 1+ year(s) |
Major Responsibilities: Provide training to new employees on cGMP concepts, SOPs, Batch Record execution, Batch record reviews, and Investigations. Basic understanding and knowledge of techniques, instrumentation, and lab functions to identify problems and support the completion of work assignments. Review proposed SOP revisions and provide feedback to management. Real-time audit of batch records in the production suites for completeness, documentation, calculation errors and conformance to critical process parameters. etc. | 7/28/2020 |
| 986 | APi North Augusta, SC Purification Chemist BS in chemistry or related Exp: Entry level |
Primary Responsibilities: 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. etc. | 7/28/2020 |
| 987 | APi North Augusta, SC MFG - Laboratory Technician HS diploma or equivalent Exp: Entry level |
Primary Responsibilities: Must manage and organize the glass cleaning operation according to approved standard operating procedures. Must manage time well. Must be able to perform daily tasks in a timely manner – improving productivity while minimizing idle time. Follow approved GMP manufacturing directions such as standard operating procedures and other instructions in support of production. Responsible for documenting all production operations in logbooks and/or batch records. Perform the scheduled clean room cleaning activities as described by the standard operating procedure. etc. | 7/28/2020 |
| 988 | APi North Augusta, SC QC Associate Microbiologist I or II BS in microbiology or other life sciences Exp: 1-5 year(s) |
Primary Responsibilities: Sampling and testing of city and pharmaceutical grade water per USP guidelines, SOP and Test method for bioburden, TOC, conductivity and endotoxin. Testing of product for release and stability for bioburden and endotoxin per USP guidelines, Test Method and SOP; endotoxin testing includes gel clot, chromogenic and turbidimetic. Bioburden testing includes method verification per USP <61>. Environmental monitoring sampling (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. etc. | 7/28/2020 |
| 989 | APi North Augusta, SC MFG Cleaning Technician HS diploma or equivalent Exp: Entry level |
Perform scheduled cleaning of all water rooms. Perform scheduled cleaning of all Lyophilizer mechanical area. Help perform daily POU Flushes and twice a week POU Sanitizations. Perform any non-GMP cleaning as assigned. Must have good time management skills. Must be able to perform daily tasks in a timely manner – improving productivity while minimizing idle time. Follow approved GMP manufacture directions such as standard operating procedures and other instructions for in support of production. Responsible for documenting all production operations and cleaning activities in logbooks and/or batch records. etc. | 7/28/2020 |
| 990 | AmbryGenetics Aliso Viejo, CA QA Engineer I BS/BA in an engineering or computer related discipline Exp: 1+ year(s) |
The Quality Assurance (QA) Engineer for Bioinformatics is responsible to create and execute software test plans from the bioinformatics pipeline requirements, specifications and test strategies. The QA Engineer works with the bioinformatics team to define attainable testing goals and relay any issues from testing back to the team. Duties and Responsibilities: Create and execute software test plans for bioinformatics pipeline/software development process. Write test reports and communicate with technical and non-technical people. Identify, isolate, and track bugs throughout testing cycles and perform automated and manual testing and identify existing and potential issues. etc. | 7/28/2020 |
| 991 | American Regent New Albany, OH Maintenance Technician - 2nd Shift HS diploma or equivalent Exp: 1+ year(s) |
A technical position involving equipment repairs and maintenance activities intended to keep the facility equipment (i.e. process, utility, and general equipment) within compliance of cGMPs. Essential Duties and Responsibilities: Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time. Perform Preventative Maintenance Tasks: Follow written PM procedures. Accurately complete PM paperwork, including work orders and logbooks in accordance with existing company policies, procedures, and Current Good Manufacturing Practices, health and safety requirements. Perform PM of all types of plant equipment including coordinating access to equipment working around customer’s needs. etc. | 7/28/2020 |
| 992 | Ampac Fine Chemicals Rancho Cordova, CA Operations Technician 1 HS diploma or equivalent Exp: 1-4 year(s) |
Operations Technician I will perform multiple duties related to the production of chemicals using a series if chemical processes in a batch type or continuous process chemical plant. These duties require careful observation and recording of data during all steps of the process. Little or no supervision required. Must have good technical and interpersonal skills to lead, direct, and instruct other employees. Some independent decision making will be required. May also be required to perform other duties in support of the plant activities not covered in another classification, including team participation. Assists in assigning tasks to other technicians, monitors performance of personnel, ensures that personnel follow all departmental and AFC policies and procedures, interacts with other personnel of other disciplines, participates in training fellow employees, conveys and logs status of processes, facilities, and personnel to the Crew Chief. etc. | 7/28/2020 |
| 993 | Ampac Fine Chemicals Rancho Cordova, CA Quality Chemist I BS in chemistry or related Exp: 1-3 year(s) |
Duties: Perform analytical chemistry analyses in accordance with company SOPs and protocols following cGMP guidelines. Log-in samples. Work with potent chemical reagents and standards. Summarize data into reports. Ability to multi-task. Performs special projects as assigned. Test and analyze samples within the specified turn-a-round time. etc. | 7/28/2020 |
| 994 | Amri Albany, NY Research Scientist I - Small Scale Manufacturing BS in organic chemistry Exp: Entry level |
Research Scientist I (Small Scale Manufacturing) in Albany, New York AMRI provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The Research Scientist I (Small Scale Manufacturing) is an integral part of the AMRI team, contributing to our success by being part of a multi-disciplinary team, committed to the safe manufacture of active pharmaceutical ingredients (APIs) for use in human clinical trials. Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. etc. | 7/28/2020 |
| 995 | Amri Albany, NY Laboratory Technician - Analytical Development AS/BS in a science Exp: 1-2 year(s) |
In this role, you will: Conduct laboratory operations in a safe manner. Maintain familiarity with the Chemical Hygiene Plan. Exhibit safety awareness and safe work practices. Follow responsible actions regarding chemical disposal. Maintain compliance with all regulations at the federal, state, and local levels, as well as all appropriate SOP’s. Develop and maintain working knowledge of commonly used spectroscopic and physiochemical procedures. Analyze samples with the standard procedures effectively and under minimal supervision. Analyze experimental data for validity before reporting results. Keep contemporary, accurate, legible, and complete experimental records in accordance with GMP and GLP practices. etc. | 7/28/2020 |
| 996 | Amri Springfield, MO Trainee, Chemical Operator HS diploma or equivalent Exp: Entry level |
In this role, you will: Safely manufacture fine chemicals. Intermediates and API manufacturing. Handle the various unit operations (reactions, filtration, distillation, drying, milling, etc.) that are performed on raw materials and various stages of chemical processing according to written manufacturing procedures and SOP’s. Follow and document per batch sheet instructions to produce product according to all cGMP guidelines. Ability to set-up equipment (vessels, tanks, centrifuges, dryers, etc.) for proper processing, Clean and verify equipment and vessels. Record observations of operating conditions. etc. | 7/28/2020 |
| 997 | Amri Lebanon, NJ Quality Control Analyst I BS in engineering or related Exp: Not necessary for BS candidates |
In this role, you will; Assist with developing and validating test methods based on relevant ISO, ASTM standards and or client requirements. Independently perform tests per ISO, ASTM, and/or client requirements. Perform testing within the specified test plan and/or SOP for each test. Monitor projects for conformance with applicable SOPs and test specifications. Prepare test specimens for package/material/device testing. Manage multiple projects/tests at any one time ensuring all commitments are met. Collaborate with and train other laboratory staff on a project basis as appropriate. Document results and review data. etc. | 7/28/2020 |
| 998 | Amri Springfield, MO Trainee, Chemical Operator HS diploma or equivalent Exp: Entry level |
In this role, you will: Safely manufacture fine chemicals intermediates and API manufacturing. Handle the various unit operations (reactions, filtration, distillation, drying, milling, etc.) that are performed on raw materials and various stages of chemical processing according to written manufacturing procedures and SOP’s. Follow and document per batch sheet instructions to produce product according to all cGMP guidelines. Ability to set-up equipment (vessels, tanks, centrifuges, dryers, etc.) for proper processing, Clean and verify equipment and vessels. Record observations of operating conditions. etc. | 7/28/2020 |
| 999 | Amri Buffalo, NY Research Scientist I - Medicinal Chemistry BS/MS in chemistry or related Exp: 0-5 years |
Research Scientist I in Albany, NY AMRI provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The Research Scientist I is an integral part of the AMRI 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. In this role, you will: Synthesize compounds efficiently using literature or in-house notebook procedures. Purify synthesized chemicals to an appropriate degree. The scientist will be able to use the full range of chromatographic, crystallization, and distillation techniques. etc. | 7/28/2020 |
| 1000 | Amri Albuquerque, NM Microbiologist I BS in a life science or related Exp: 0-2 years |
Albany Molecular Research Inc. provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. Summary: Prepare, collect, and test plant purified water, manufacturing raw materials, product in-process, and finished product, and perform environmental monitoring. With limited supervision, learn and perform critical laboratory techniques and complete original work. Author problem reports and participate in investigations. This description is inclusive of EM and testing duties: actual percentages of time spent on each duty may vary based on business needs. etc. | 7/28/2020 |
| 1001 | ARL BioPharma Oklahoma City, OK Sample Administrator I - Part Time HS diploma or equivalent Exp: 0-2 years |
Occupations that fit well with this position are pharmacy technician and medical office administrative assistant. The job is performed in an office environment. This position is to perform all data entry processes needed or required to facilitate the accurate reporting of all samples submitted for testing. The Accessioner maintains sample integrity to ensure accurate and timely testing and reporting by the appropriate lab. Additionally, the Accessioner may perform other duties requested by the Accessioning Supervisor. Minimal to moderate supervision is required. etc. | 7/28/2020 |
| 1002 | AngioDynamics Queensbury, NY Associate IT Service Desk Technician HS diploma or equivalent Exp: 0+ years |
Triage and resolve incidents, problems, and requests efficiently using our ITSM tool. Configure, install, and troubleshoot software, laptops, desktops, IP phones, mobile devices, printers, and other computer peripherals. Provide timely support onsite, remotely, and over the phone as part of our global IT call center. Perform after-hours work as needed on a rotating schedule. Procure standardized hardware and software from vendors, escalating non-standard requests to leadership. Follow change procedures for employee events (new hires, terminations, transfers, promotions, etc.). Assign roles and permissions to network resources such as SharePoint sites, file shares, and ERP systems. etc. | 7/28/2020 |
| 1003 | AMT Brecksville, OH Essential Detailed Device Assembly- 1st Shift HS diploma or equivalent Exp: 0-2 years |
Assembly of Percutaneous Endoscopic Gastrostomy (PEG) devices or products using like materials/components/assembly procedures. Duties and Responsibilities: This list is not comprehensive but meant to represent the most common or important duties of the position. Other duties are required and/or assigned. Hand assembly and gluing of components. Use of manual and semiautomatic fixtures. Inspection of assembled components. Maintain quality and efficiency standards. Complete paperwork accurately and legibly. Cross-functional training required. etc. | 7/28/2020 |
| 1004 | AMT Brecksville, OH Essential Detailed Device Assembly- 2nd shift HS diploma or equivalent Exp: 0-2 years |
Assembly of Percutaneous Endoscopic Gastrostomy (PEG) devices or products using like materials/components/assembly procedures. Duties and Responsibilities: This list is not comprehensive but meant to represent the most common or important duties of the position. Other duties are required and/or assigned. Hand assembly and gluing of components. Use of manual and semiautomatic fixtures. Inspection of assembled components. Maintain quality and efficiency standards. Complete paperwork accurately and legibly. Cross-functional training required. etc. | 7/28/2020 |
| 1005 | AMT Brecksville, OH Essential Entry Level Injection Molding Machine Operator-1st Shift HS diploma or equivalent Exp: Entry level |
Operates injection molding machines according to specific schedules and procedures. Prepares mold inserts and reviews molded component integrity. Duties and Responsibilities: This list is not comprehensive but meant to represent the most common or important duties of the position. Other duties are required and/or assigned. Remove molded components from the mold once the machine has finished its cycle. Prepare cores and mold for next cycle. When applicable test parts during machine cycle to predetermined specifications. Inspect parts for overall integrity while machine is cycling. Maintain quality and efficiency standards. Use of manual and semiautomatic fixtures. Complete paperwork accurately and legibly. etc. | 7/28/2020 |
| 1006 | AMT Brecksville, OH Essential Entry Level Injection Molding Machine Operator-2nd Shift HS diploma or equivalent Exp: Entry level |
Operates injection molding machines according to specific schedules and procedures. Prepares mold inserts and reviews molded component integrity. Duties and Responsibilities: This list is not comprehensive but meant to represent the most common or important duties of the position. Other duties are required and/or assigned. Remove molded components from the mold once the machine has finished its cycle. Prepare cores and mold for next cycle. When applicable test parts during machine cycle to predetermined specifications. Inspect parts for overall integrity while machine is cycling. Maintain quality and efficiency standards. Use of manual and semiautomatic fixtures. Complete paperwork accurately and legibly. etc. | 7/28/2020 |
| 1007 | AMT Brecksville, OH Essential Light Assembly Associate - 1st Shift HS diploma or equivalent Exp: Entry level |
Assembly of feeding sets and other basic assemblies or products using like materials/components/assembly procedures. Duties and Responsibilities: This list is not comprehensive but meant to represent the most common or important duties of the position. Other duties are required and/or assigned. Visual inspection of devices, labels, and packaging. Use of manual and semiautomatic fixtures. Inspection of assembled components. Maintain quality and efficiency standards. Complete paperwork accurately and legibly. Cross-functional training required. etc. | 7/28/2020 |
| 1008 | AMT Brecksville, OH Essential Light Assembly Associate- 2nd Shift HS diploma or equivalent Exp: Entry level |
Assembly of feeding sets and other basic assemblies or products using like materials/components/assembly procedures. Duties and Responsibilities: This list is not comprehensive but meant to represent the most common or important duties of the position. Other duties are required and/or assigned. Visual inspection of devices, labels, and packaging. Use of manual and semiautomatic fixtures. Inspection of assembled components. Maintain quality and efficiency standards. Complete paperwork accurately and legibly. Cross-functional training required. etc. | 7/28/2020 |
| 1009 | AMT Brecksville, OH Essential Molding Machine Operator- 3rd Shift HS diploma or equivalent Exp: Entry level |
Operates injection molding machines according to specific schedules and procedures. Prepares mold inserts and reviews molded component integrity. Duties and Responsibilities: This list is not comprehensive but meant to represent the most common or important duties of the position. Other duties are required and/or assigned. Remove molded components from the mold once the machine has finished its cycle. Prepare cores and mold for next cycle. When applicable test parts during machine cycle to predetermined specifications. etc. | 7/28/2020 |
| 1010 | Archer Boulder, CO Quality Control Associate BS Exp: 1-3 year(s) |
Job performance will involve a variety of activities including: Execution of work instructions for testing raw materials, in-process materials/sub-assemblies, and top-level IVD materials to determine compliance to specifications. Critical analysis of data ensuring compliance with standards and specifications. Generation of data reports. Adherence to safety and quality laboratory standards. Upkeep of personal training and associated records. Maintenance of laboratory material stocks and initiation of re-orders. Execution of method validation and stability testing protocols. Identification of non-conforming material and subsequent report initiation and generation (OOS/OOT investigation). etc. | 7/28/2020 |
| 1011 | Argon Medical Devices Athens, TX Manufacturing Engineer I BS in mechanical or industrial engineering Exp: 1-2 year(s) |
The Manufacturing Engineer will be responsible for leading and participating in creating, finding, and evaluating better and more efficient ways to manufacture products and provide ongoing production support for Argon Medical products and manufacturing sites. The Manufacturing Engineer will work to manage and communicate progress towards project goals to management effectively. The Manufacturing Engineer will work to gather and document customer requirements, translate them into measurable product requirements, and provide engineering support for the development and manufacture of Argon Medical Device products. etc. | 7/28/2020 |
| 1012 | Argonaut Manufacturing Services Carlsbad, CA Technical Transfer Operator, Drug Product Manufacturing BS in a life science or engineering Exp: 1-3 year(s) |
The purpose of this position is to transfer product and process knowledge from developmental clinical production to GMP product manufacturing in the drug product manufacturing division of Argonaut. Responsibilities: Facilitate transfer of new processes from client lab or concept to drug product manufacturing by collaborating with subject matter experts and operations management. Participate in client discussions via phone, video conference, and/or onsite visits. Create and revise client-specific batch records, raw material specifications, and any documentation related to Drug Product Manufacturing. Review executed batch records and other documentation, as needed. etc. | 7/28/2020 |
| 1013 | Arthrex Ave Maria, FL Laser Machine Operator I- Second Shift HS diploma or equivalent Exp: 6+ months |
Main Objective: To produce superior products following Arthrex Manufacturing Inc. machining processes and procedures. This position is eligible for a sign-on bonus. If you are hired, you will be eligible for a $750.00 sign-on bonus (minus appropriate tax withholdings) paid after you complete your first 90 days and are an employee in good standing. Essential Duties and Responsibilities: Operation of Assembly, Laser Mark, Laser Weld, and EDM equipment in accordance to work instructions. Inspect machined work piece to specifications, based on correct AQL. Verify inspection tools issued to job are available and correct. Receives and verifies work order and verifies that the components are correct. Notifies Supervisor or Lead if equipment is not operating properly. etc. | 7/28/2020 |
| 1014 | Arthrex Ave Maria, FL Textile Technician - 2nd Shift HS diploma or equivalent Exp: 1 year |
Arthrex Manufacturing is hiring additional team members to the Textile department on second shift. The Textile Technician is responsible for setting and operating machines that produce the materials for the Sutures department. The second shift hours are 4:00 pm to 12:30 am, Monday through Friday. Training will be on first shift for approximately 8 weeks. The job location will be at the Arthrex manufacturing facility in Ave Maria, FL. Essential Duties and Responsibilities: Set-up and operate a variety of hand tools and light duty textile machines to manufacture product specified on work order using engineering prints, standard work instructions and Inspection procedures. Manufacture the finished product to specifications with the use of measuring equipment, specialized hand tools and microscopes, making decisions in equipment setup parameters within established guidelines to achieve the required specifications. etc. | 7/28/2020 |
| 1015 | Accelerate Diagnostics Tucson, AZ Research Associate, Quality Control BS in chemistry, microbiology, biochemistry, molecular biology, or related Exp: 1+ year(s) |
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, HPLC-MS, 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. etc. | 7/22/2020 |
| 1016 | Accuray Madison, WI Microwave Technician/CNC Welder AS in production, manufacturing or general engineering Exp: Not necessary for AS candidates |
The Technician is responsible for the re-manufacture and repair activities of linear accelerators (linacs) that allow Accuray to provide products that meet customer needs and do so in accordance with regulatory requirements. ESSENTIAL DUTIES AND RESPONSIBILITIES: Performs CNC machining operations in the Linac Repair Center. Performs precision Tungsten Inert Gas (TIG) welding of copper, Kovar, and stainless steel. Investigates field returns to decide what the failure was and what actions need to be taken for repair. Assembles and disassembles linear accelerators in accordance with schedule and in accordance with quality system requirements, procedures, and work instructions. Uses Rf equipment for tuning of linear accelerators. etc. | 7/22/2020 |
| 1017 | Acell Columbia, MD Biotechnician HS diploma or equivalent Exp: Entry level |
This is an entry level position for a Biotechnician. Employee will carry out manufacturing practices in a cGMP biotechnical facility. The job involves the manual processing of porcine urinary bladders, which includes all aspects from collection of raw materials to packaging of the final product. Following training, work will be expected to be performed independently to a high degree of standard in biomaterial handling. Principal Responsibilities: Collection of raw materials. Rinse and initial cleaning of raw materials upon receipt. Separation and removal of unwanted tissues. Disinfection. Preparation of storage and cleaning solutions. etc. | 7/22/2020 |
| 1018 | Acell Lafayette, IN Biotechnician - Second Shift HS diploma or equivalent Exp: Entry level |
This is an entry level position for a Biotechnician. Employee will carry out manufacturing practices in a cGMP biotechnical facility. The job involves the manual processing of porcine urinary bladders, which includes all aspects from collection of raw materials to packaging of the final product. Following training, work will be expected to be performed independently to a high degree of standard in biomaterial handling. Principal Responsibilities: Collection of raw materials. Rinse and initial cleaning of raw materials upon receipt. Separation and removal of unwanted tissues. Disinfection. Preparation of storage and cleaning solutions. etc. | 7/22/2020 |
| 1019 | Acella Pharmaceuticals Dallas, TX Pharmaceutical Sales Representative (NP) BS/BA Exp: 1 year |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN & Rheumatology offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. Responsible for providing healthcare providers with all relevant information that promotes quality healthcare decisions. Employ effective selling techniques, including pre-call planning, effective opening, presentation focus, productive questions, issues identification and effective close. etc. | 7/22/2020 |
| 1020 | Acumed Wichita, KS Sales Associate, Wichita, Kansas - Future Opportunities BS/BA in a business or medical discipline Exp: 0-3 years |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. Continuously assesses the customer base to identify new business opportunities and develops a targeted sales strategy for each identified opportunity proactively ensuring all leads are followed up on appropriately. etc. | 7/22/2020 |
| 1021 | Acumed Hillsboro, OR Quality Engineer I BS in engineering or a science Exp: 1-3 year(s) |
The Quality Engineer is responsible for providing Quality Assurance support to product development and manufacturing to increase product quality, reliability, and process capability. Responsible for identifying, documenting, assessing, correcting and presenting quality issues using risk and root cause analysis tools. Supports quality of new products being released to the market through participation in the product development process to ensure product and process conformance to global standards (including FDA and ISO 13485). Serves as a quality representative to design control, verification and validation, design transfer, and risk management on assigned product development teams ensuring compliance with Acumed policies and global regulations, including FDA Quality System Regulation and ISO 13485. etc. | 7/22/2020 |
| 1022 | Acumed Kansas City, KS Associate Sales Representative - Kansas City, KS BS in engineering or a science Exp: 0-2 years |
The Associate Sales Representative (ASR) exceeds sales quota within an assigned territory by delivering Acumed product on time and providing high quality technical assistance in the OR. The ASR assists in the assessment of the customer base to identify new business opportunities and executes a targeted sales strategy for each identified opportunity proactively ensuring all leads are followed up on appropriately. Duties/Responsibilities: Execute business plans to identify and close new business. Identifies the needs of new prospects and develops/delivers appropriate responses to meet or exceed needs (written, telephone and face-to-face). etc. | 7/22/2020 |
| 1023 | Adaptive Biotechnologies Seattle, WA Clinical Laboratory Technologist I - PCR/Sequencing (Sun-Wed PM) BS/MS in a chemical, physical, or biological science Exp: 1+ year(s) |
The Clinical Laboratory Technologist 1 position will be responsible for processing medically relevant biological samples through extraction or high throughput DNA sequencing assays. This role will work within a team of Laboratorians in a fast-paced, high production setting to process research and clinical diagnostic samples to provide a test result to patients, oncologists and other medical practitioners and researchers. As such, high attention to detail and clinical mindedness are crucial to success in this role. Responsibilities: Assignment to one of two labs performing either DNA extractions from human biological samples, or PCR amplification and high-throughput sequencing assays on DNA libraries. Demonstrate good clinical judgment and integrity. Perform DNA extractions, PCR amplification or high-throughput sequencing assays on DNA libraries. etc. | 7/22/2020 |
| 1024 | Adaptive Biotechnologies Seattle, WA Clinical Laboratory Technologist I - PCR/Sequencing (Sun-Wed AM) BS/MS in a chemical, physical, or biological science Exp: 1+ year(s) |
The Clinical Laboratory Technologist 1 position will be responsible for processing medically relevant biological samples through extraction or high throughput DNA sequencing assays. This role will work within a team of Laboratorians in a fast-paced, high production setting to process research and clinical diagnostic samples to provide a test result to patients, oncologists and other medical practitioners and researchers. As such, high attention to detail and clinical mindedness are crucial to success in this role. Responsibilities: Assignment to one of two labs performing either DNA extractions from human biological samples, or PCR amplification and high-throughput sequencing assays on DNA libraries. Demonstrate good clinical judgment and integrity. Perform DNA extractions, PCR amplification or high-throughput sequencing assays on DNA libraries. etc. | 7/22/2020 |
| 1025 | Adaptive Biotechnologies Seattle, WA Clinical Laboratory Technologist I - Extraction (Thurs-Sat PM) BS/MS in a chemical, physical, or biological science Exp: 1+ year(s) |
The Clinical Laboratory Technologist 1 position will be responsible for processing medically relevant biological samples through extraction or high throughput DNA sequencing assays. This role will work within a team of Laboratorians in a fast-paced, high production setting to process research and clinical diagnostic samples to provide a test result to patients, oncologists and other medical practitioners and researchers. As such, high attention to detail and clinical mindedness are crucial to success in this role. Responsibilities: Assignment to one of two labs performing either DNA extractions from human biological samples, or PCR amplification and high-throughput sequencing assays on DNA libraries. Demonstrate good clinical judgment and integrity. Perform DNA extractions, PCR amplification or high-throughput sequencing assays on DNA libraries. etc. | 7/22/2020 |
| 1026 | Adare Pharmaceuticals Vandalia, OH Document Control Specialist I BS/BA Exp: Not necessary for BS/BA candidates |
Responsible for conducting day to day quality documentation processing for cGMP documents, and provide support to internal end users on document management processes. ESSENTIAL DUTIES AND RESPONSIBILITIES: The primary duties and responsibilities of this position include the following. Other duties may be assigned. Formats, tracks and issues controlled cGMP documents. Assist in review of cGMP controlled documents as necessary. Issuance of batch production records, tracking of master batch records, and tracking of all batch production records. Supports quality audits (internal and external), troubleshooting efforts, and other Quality System processes. Evaluates issues received from end users and makes decision on appropriate follow-up steps. Scan, image, organize and maintain documents, adhering to the company's document lifecycle procedures, and they archive inactive records in accordance with the records retention schedule. Maintains filing of all master documents. Maintains an efficient and easily retrievable documentation system for all the documents. etc. | 7/22/2020 |
| 1027 | Adare Pharmaceuticals Vandalia, OH Analytical Scientist I BS/MS in chemistry or the physical sciences Exp: Entry level |
The essential job function is to 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. ESSENTIAL DUTIES AND RESPONSIBILITIES: The primary duties and responsibilities of this position include the following. Other duties may be assigned. With supervision and direction the analyst is required to: Provide support for the development and validation of pharmaceutical analytical methods for potency, dissolution, impurities/degradation products, residual solvents…using appropriate laboratory instrumentation e.g. HPLC, UHPLC, LC-MS, Dissolution Apparatus, GC… etc. | 7/22/2020 |
| 1028 | Admera Health South Plainfield, NJ Associate Scientist I/II-Lab BS/MS in biological sciences Exp: 1-3 year(s) |
Responsibilities: Preparing solutions and reagents for performing assays on the bench. Perform Next Generation Sequencing-based genomic assays on different workflows (few listed below): 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 record keeping of all laboratory procedures. etc. | 7/22/2020 |
| 1029 | ABL Rockville, MD QC Microbiologist I BA/BS in microbiology, biology, or related Exp: 1-2 year(s) |
The QC Analyst Microbiology 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. etc. | 7/22/2020 |
| 1030 | Advanced Vision Sciences Goleta, CA Bookkeeper AS/AA Exp: Not necessary for AS/AA candidates |
This position is responsible for the timely and accurate processing of payroll and maintaining payroll records; timely and accurate processing and payment of Accounts Payable and maintaining AP records; timely and accurate processing of General Ledger journal entries and Balance Sheet account reconciliations; Assist in month end close process. MAJOR DUTIES OF POSITION: Process biweekly payroll and maintain all payroll records. Prepare periodic reports of earnings, taxes and deductions. Keep record of leave pay (sick, vacations, disability). Prepare and transmits 401K spreadsheets. Prepare and uploads 125K spreadsheets. etc. | 7/22/2020 |
| 1031 | B. Braun Allentown, PA IV Tech I HS diploma or equivalent Exp: 1+ year(s) |
Prepares compounded sterile products and performs related activities under the direction of a pharmacist. Responsibilities: Essential Duties: Prepares compounded sterile products using aseptic technique. Assists in the set up of the compounding room, equipment, and supplies for preparation of compounded sterile solutions, using aseptic technique. Performs general cleaning and maintenance duties as directed. Participates in cleanroom product introduction activities. Prepares records and monitors results for pharmaceutical quality assurance testing. etc. | 7/22/2020 |
| 1032 | B. Braun Phoenix, AZ Pharmacy IV Technician HS diploma or equivalent Exp: 1+ year(s) |
Prepares compounded sterile products and performs related activities under the direction of a pharmacist. Responsibilities: Essential Duties: Prepares compounded sterile products using aseptic technique. Assists in the set up of the compounding room, equipment, and supplies for preparation of compounded sterile solutions, using aseptic technique. Performs general cleaning and maintenance duties as directed. Participates in cleanroom product introduction activities. Prepares records and monitors results for pharmaceutical quality assurance testing. etc. | 7/22/2020 |
| 1033 | B. Braun Irvine, CA PMO Analyst I BS/BA Exp: 0-2 years |
Responsibilities: Essential Duties: Under the direction of the PMO Manager, supports the Project Management Office (PMO) related activities to ensure the success of the PMO and its objectives. Works collaboratively in a team environment (Corporate, Manufacturing, Quality, Operations, Supply Chain, Procurement, Engineering, etc.) in support of PMO activities. Collaborates with Project Leaders to update and manage the project portfolio data and capital spend and forecast data via spreadsheet and the project portfolio management system (PPMS). Supports the creation and maintenance of key project portfolio metrics using Excel, Powerpoint, and other tools to provide visibility to management. etc. | 7/22/2020 |
| 1034 | B. Braun Irvine, CA Product Handler (Excel Filling Pooling) HS diploma or equivalent Exp: 0-4 years |
Responsibilities: Essential Duties: Assists supervisor to ensure that production operators have sufficient stock of materials. Collects, checks and keeps records of materials flow to and from production area. Etc. | 7/22/2020 |
| 1035 | Ajinomoto Bio-Pharma Services San Diego, CA Temporary Drug Product Support Technician HS diploma Exp: 0-1 year(s) |
We are currently seeking multiple Temporary Drug Product Support Technicians to join the team. In this role you will be responsible for packing and labeling and offload activities for our various drug products. Responsibilities: Operates filled drug product offloading equipment. Accurate receipt and counting of filled units from Fill Finish manufacturing. Responsible for product transfers to Materials Management. Responsible for assisting with pre and post Line Clearance, and Good Documentation Practices (GDP). H24Perform Bulk Packaging and Labeling of Vials or Syringes. Follow all proper gowning procedures. etc. | 7/22/2020 |
| 1036 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Manufacturing Assistant HS diploma/BS in a life science Exp: 0-2 years |
We are looking for multiple Drug Product Manufacturing Assistants for 1st Shift! The Drug Product Manufacturing Assistant is responsible for implementation of routine production and manufacturing procedures to optimize processes and regulatory requirements. Responsibilities: Performs various routine manufacturing tasks under the guidelines of established SOP’s and cGMP regulations. Implements production and manufacturing procedures. Performs visual inspection. Prepares components, media, buffers, and other solutions as needed. Accurately documents data and completes batch records as needed. May cross train and/or focus in various manufacturing tasks including fill/finish, formulation, fermentation, preparation. Operates production equipment and may prepare buffers and media, inspect, label, or box. etc. | 7/22/2020 |
| 1037 | Agilent Santa Clara, CA Business Process Associate BS/BA/MS/MA Exp: 1+ year(s) |
The Business Process Associate role reports into the Global Sales Enablement (GSE) team, which supports LSS Global Sales and Marketing functions. This team collaborates cross-functionally with sales, marketing, service, SUs and other supporting organizations, to effectively execute strategic LSS and Corporate programs across the world. We're looking for a talented and motivated professional to join the team. Responsibilities include: Responsible for analysis and evaluation of user business problems and development of business system or process recommendations to meet requirements, including problem definition, evaluation of requirements, and implementation of systems/processes. etc. | 7/22/2020 |
| 1038 | Akorn Amityville, NY Metrologist AS/AA in instrumentation engineering Exp: Not necessary for AS/AA candidates |
The Calibration Technician is responsible for the following activities: Ability to perform all Calibration Technician I functions. Ability to work independently installing, troubleshooting, and calibrating all types of instruments or control systems in any Akorn environment. Maintain calibration records and enter calibration data using software such as Calibration Manager. Daily review and update the calibration validation data. Fluently use software such as MS Excel, Word, and other maintenance manager software such as AMMS to purchase items and complete validation documentation. Develop SOPs for new or existing equipment as required. Coordinate equipment calibrations for equipment to be calibrated. etc. | 7/22/2020 |
| 1039 | Akorn Somerset, NJ Production Line Operator (3 pm - 11:30 pm) HS diploma or equivalent Exp: 1 year |
All Production Line Operators are responsible for all activities associated with the manufacturing and filling operations, required to produce sterile drug products under aseptic conditions. ESSENTIAL FUNCTIONS: Include the following. Other duties may be assigned. Compliance with associated SOPs and training requirements. Basic understanding of personnel, equipment flow and controlled environments. Prepare for aseptic gowning qualifications. NOTE: Must have flexibility, discipline and not fall out of established limits. Basic understanding of aseptic procedures and cleanroom behavior in controlled environments. Transport sterile components and supplies from a controlled 10000 classification environment to a 1,000 classification environment and from 1,000 classification environment to 100 classification environment. Observation and processing of fills/rooms in #1 and #2 areas. etc. | 7/22/2020 |
| 1040 | Akorn Decatur, IL 2nd shift Production Technician – Lead HS diploma or equivalent Exp: Not necessary |
Direct oversight of assigned production fill room, equipment preparation or glassware preparation employees. Carries out leadership responsibilities in accordance with the organization’s policies and applicable laws. Responsibilities include training employees; planning, assigning, and directing work; appraising performance; addressing complaints and resolving problems. Must be able to communicate effectively with all levels of employees. Must be able to perform simple math calculations. Must be able to solve problems, handle conflict, and make effective decisions under pressure. ESSENTIAL LEAD TECHNICIAN DUTIES AND RESPONSIBILITIES: Include the following. Other duties may be assigned. Provide oversight of the Key Process Steps; i.e., equipment set up and alignment, defined line speed, hold times, machine prime, etc. In addition: Media fill completed in strict adherence to the Batch Record and Media SOP requirements. etc. | 7/22/2020 |
| 1041 | Akorn Somerset, NJ Production Line Operator (2nd Shift - 6 pm - 2:30 am) HS diploma or equivalent Exp: 1 year |
All Production Line Operators are responsible for all activities associated with the manufacturing and filling operations, required to produce sterile drug products under aseptic conditions. ESSENTIAL FUNCTIONS: Include the following. Other duties may be assigned. Compliance with associated SOPs and training requirements. Basic understanding of personnel, equipment flow and controlled environments. Prepare for aseptic gowning qualifications. NOTE: Must have flexibility, discipline and not fall out of established limits. Basic understanding of aseptic procedures and cleanroom behavior in controlled environments. Transport sterile components and supplies from a controlled 10000 classification environment to a 1,000 classification environment and from 1,000 classification environment to 100 classification environment. Observation and processing of fills/rooms in #1 and #2 areas. etc. | 7/22/2020 |
| 1042 | Akorn Decatur, IL 2nd shift Environmental Monitoring Technician HS diploma or equivalent Exp: 1 year |
The Environmental Monitoring Technician I will perform all environmental monitoring tests required to monitor the manufacturing controlled areas at Akorn’s Grand Avenue facility. ESSENTIAL FUNCTIONS: Include the following. Other duties may be assigned. Must be able to demonstrate and apply good aseptic technique and cleanroom behavior. Must be able to demonstrate and apply good gowning technique during certification, re-certification, and routine monitoring. Must be able to understand the operation and application of all monitoring devices that are automated or manual operation in the department. Must be able to demonstrate the ability to monitor and document all environmental parameters, such as viable sampling, personnel sampling, temperatures, humidity, and differential pressures under static and dynamic conditions. Fill out cleanroom information sheets. etc. | 7/22/2020 |
| 1043 | Alcami Charleston, SC Environmental Monitoring Tech I- 3rd Shift BS/BA Exp: 0-2 years |
The Environmental Monitoring Technician I is accountable 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-negotiables, as well as the functional competencies of this profile. Essential Functions: Performs routine daily, weekly and monthly sampling of Water for Injection, compressed gas and the environment to detect microbial, non-viable and chemical contamination. Supports manufacturing operations by continuous environmental monitoring viable and non-viable particles. etc. | 7/22/2020 |
| 1044 | Alcami Germantown, WI Regulatory Affairs Specialist I BS/MS in science or engineering Exp: 1+ year(s) |
The Regulatory Affairs Specialist is accountable for driving results in a fast-paced environment by performing activities to ensure that regulatory submissions support active pharmaceutical ingredient (API) business needs and that the business remains compliant with regulatory filings. Activities include preparation and submission of regulatory filings, written and verbal communication with regulatory agencies and clients, and providing regulatory affairs information and counsel to other site functions. 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. Essential Functions: Remain informed about regulations and regulatory trends concerning US FDA and other countries’ regulatory agencies. etc. | 7/22/2020 |
| 1045 | Alcami Charleston, SC Manufacturing Tech- 3rd Shift HS diploma/AS/AA Exp: 0-2 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. etc. | 7/22/2020 |
| 1046 | Alcami Morrisville, NC Manufacturing Tech I HS diploma/AS/AA Exp: 0-2 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. etc. | 7/22/2020 |
| 1047 | Alcami Charleston, SC Manufacturing Tech- Weekend Shift HS diploma/AS/AA Exp: 0-2 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. etc. | 7/22/2020 |
| 1048 | Alcami Charleston, SC Material Control Tech I HS diploma/AS/AA Exp: 0-2 years |
The Materials Control Technician I is accountable for results in a fast-paced environment by following applicable SOPs and cGMPs to perform tasks for the receipt, storage, inventory and distribution of raw materials, intermediate or finished drugs or drug products and components. The Materials Control Technician I uses the electronic inventory system to track, document and control all inventory. 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. etc. | 7/22/2020 |
| 1049 | Alkermes Wilmington, OH Training Technology Specialist I BS in information technology Exp: 1-3 year(s) |
This position supports the Operations Training Group in use of technology software, hardware, applications, video, etc.… for training development and delivery. Supports the development of content for the departmental training materials for Good Manufacturing Practices (GMP) training. Provides basic information technology training classes and training resources to departmental areas of responsibility. Provides training information technology guidance to area trainers and maintains/updates the departmental Sharepoint site. This position supports a comprehensive operations training strategy that aligns to the departmental talent strategies and supports the overall organizational strategy. etc. | 7/22/2020 |
| 1050 | Alkermes Wilmington, OH QC Analyst II - Micro BS in biology, microbiology, biotechnology, biochemistry Exp: 1 year |
QC Analyst Il must have broad knowledge of all the 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, data entry and occasional review of data for finished product, in-process samples, stability samples, clinical materials and raw material release in a cGMP regulated environment. Major Responsibilities: Execution of microbiological tests including but not limited to bioburden, LAL, growth promotion, sterility, particulate profiling and microbial identification of bulk, raw materials, in-process material, components, clinical materials and finished product. If required, must be able to perform cGMP biological testing (bioassays, flow cytometry, qPCR, and ELISA). Review and data entry for testing results following GMP regulations into the electronic data management systems. etc. | 7/22/2020 |
| 1051 | Alkermes Wilmington, OH QA Associate I/II BS Exp: 1-2 year(s) |
This function is responsible for supporting the daily on the floor activities related the manufacturing operations and quality systems. Functions include on the floor batch record review, discrepancy identification, logbook review, status tagging, room/utility checklists, document control and product shipping. This function thresholds events to Senior Associate when they are outside of the area of responsibility. The position will perform general QA work, using their ability as a skilled contributor in completing tasks where judgement is required in resolving problems and making recommendations. Works on problems of a diverse scope where analysis and problem solving is required. Receives general oversight and guidance on approaches to complete project related tasks. Applies job related skills and understanding of policies and standards in completing tasks. etc. | 7/22/2020 |
| 1052 | B. Braun Irvine, CA Machine Attd (Titan Filling) HS diploma or equivalent Exp: 1-5 year(s) |
Responsibilities: Essential Duties: Follows established procedures and guidelines to manufacture the organization's products according to production specifications and schedules, volume, cost, and wastage targets or quality standards. Operates machines and production equipment safely and in accordance with instructions. Monitors the quality of output to identify, discard or remanufacture faulty products. Maintains accurate daily production records so that manufacturing performance can be analyzed. Troubleshoots and resolves technical problems from the product line/process to minimize reject levels.-For more senior position, might act as a team leader to ensure that the work meets agreed targets by directly overseeing team members. etc. | 7/22/2020 |
| 1053 | B. Braun unspecified, US Sales Associate BS/BA Exp: 0-4 years |
The Sales Associate Program is a full time, entry-level development program designed to serve as an entry point to a career in Sales at B. Braun Medical Inc. We will provide rigorous, comprehensive, hands on training for up to 24 months. At the conclusion of the program, participants will have the opportunity to be placed in a Sales role in a dedicated geography. Program participants will have exposure to the many different elements of Sales, while learning B. Braun's processes to achieve success. There are endless opportunities to build networks, develop strong relationships, and gain credible work experience. This program enables growth and development across the Sales organization, with structured mentoring from senior account managers. etc. | 7/22/2020 |
| 1054 | B. Braun Hazelwood, MO Technician, Endoscopic HS diploma Exp: 6 months |
Summary: Responsible for repairing, refurbishing and cleaning of basic precision Endoscopic/Laparoscopic surgical instruments under supervision of lead. Principal Duties Responsibilities: Buffs, Polishes, grinds, and performs minor repairs on basic surgical instruments. Instruments include but are not limited to Aesculap Endoscopic/Laparoscopic instruments. Surface treatment. Red-wheeling and bead blasting as needed. Repair, replace, realign to complete full refurbishment of basic instrumentation. etc. | 7/22/2020 |
| 1055 | FYR Diagnostics Missoula, MT Lab Technician BS or MS in biological sciences Exp: 0-2 years in lab |
Learn laboratory-based skills and work with an interdisciplinary team investigating novel isothermal PCR-based technology. Work with other researchers and technicians to execute, analyze and interpret PCR-focused experiments and miscellaneous in vitro experiments. Preparation of reagents and samples for experiments | 7/18/2020 |
| 1056 | Fzata Halethrope, MD Administrative Assistant BS/BA Exp: 1 y ear as admin assistant |
Prepare documents, reports for managers. Schedule and coordinate meetings, travel arrangement. Data processing, input and verification. Monitor and track expenses | 7/18/2020 |
| 1057 | Cosette Pharmaceuticals Lincolnton, NC QC Auditor I (TEMP) BS or BA in chemistry Exp: 1 year in labaa auditing documentation |
The purpose of this position is to review QA/QC documentation, to assess data compliance/validity with regulatory guidelines in the Quality Control Department and ensure that all the work is performed and documented accurately, timely and in compliance with internal procedures and regulatory agencies. Provide technical support for the release of raw materials, finished products, and stability data. | 7/18/2020 |
| 1058 | Cosette Pharmaceuticals South Plainfield, NJ MANUFACTURING OPERATOR 1 HS Diploma or GED Exp: 1-2 years in cGMP |
Perform work within the manufacturing department to clean equipment/rooms, dispense, and operate equipment for product studies, development, and commercial production. | 7/18/2020 |
| 1059 | GenapSys Redwood City, CA Research Associate, Systems Integration MS in biological sciences or engineering Exp: 0-2 years in lab |
Participate in development and optimization of NGS Platform workflow steps, in order to improve the existing performance of our NGS platform. Participate in short-term and long-term exploratory studies of assay development on Genapsys platforms. Plan and execute experiments, perform in-depth data analysis and present results and conclusions for internal review, and evaluate the research of peers. | 7/18/2020 |
| 1060 | GeneDx Gaithersburg, MD Medical Lab Technologist BS in med technology, biology, or chemistry Exp: 1 year in CLIA lab |
The Medical Lab Technologist performs all laboratory procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. Maintain standards in routine & STAT testing. Complete work in a timely manner. Write legibly when documenting QC, problems or information. | 7/18/2020 |
| 1061 | GeneDx Gaithersburg, MD DNA Extraction Technician BS in medical technology or life sciences Exp: 0-1 years |
Learns and follows the established standard operating procedures for specimen handling and processing, test analysis, reporting of results to team leads, supervisors and test managers, and record-keeping. Adheres to quality control policies; documents all quality control activities, instrument and procedural calibrations, reagent preparation and testing, and instrument maintenance performed | 7/18/2020 |
| 1062 | GeneDx Gaithersburg, MD Lab Technician, Microarray BS in medical technology or life sciences Exp: 1 year in technologies |
The Laboratory Technician performs an entry level role in the testing of clinical DNA specimens for the purpose of diagnosing genetic disease, using manual and automated methods in a team environment, and following established policies and procedures in a professional manner.Implements the standard operating procedures for specimen handling and processing, test analysis, reporting of results to team leads, supervisors and test managers, and record-keeping. | 7/18/2020 |
| 1063 | Generation Bio Cambridge, MA Associate Scientist InVivo Care and Resources HS Diploma/GED or BS Exp: 1-3 years in lab animal husbandry |
Perform daily husbandry of rats and mice under modified barrier conditions and document accordingly. Monitor and document animal facility conditions including temperature and humidity daily. Perform twice daily health monitoring of animals, document and report abnormal conditions to the supervisor. Perform general upkeep and cleaning of facility including daily sweeping and mopping and quarterly cleaning | 7/18/2020 |
| 1064 | Generation Bio Cambridge, MA Associate Scientist / Senior Associate Scientist, Drug Product Formulation-CMC MS in pharmacuetics, chemical sciences/engineering Exp: 0-2 years |
Execute on development work for the manufacturing processes for Drug Product formulation using both DNA vectors and Lipid Nanoparticles (LNPs). Ensures all appropriate materials, equipment, protocols and documentation are available and completed for multiple Drug Product formulations targeted for research and pre-clinical programs. | 7/18/2020 |
| 1065 | Genewiz South Plainfield, NJ Associate Scientist I BS/BA in biological sciences Exp: 1+ year in biological laab |
Prepare amplified template libraries for high-throughput sequencing. Carry out DNA sequencing on next-generation DNA analyzers. Perform routine maintenance of DNA analyzers and related equipment. Check inventory and replenish consumable sequencing supplies. Communicate with customers by phone and e-mail in a friendly and professional manner | 7/18/2020 |
| 1066 | Neo Genomics Carlsbad, CA Logistics Technician HS Diploma/GED Exp: 1 year as accessioning technician |
The Logistics Technician will ensure proper handling of all specimens received and prepare specimens for laboratory testing. This position includes such functions as matching patient information, data entry, and scanning documents. This is entry level in the Logistics job category, and employees perform the full range of specimen processing procedures. | 7/18/2020 |
| 1067 | Neo Genomics Aliso Viejo, CA Clinical Laboratory Technologist, Molecular BS/BA in biological/chemical sciences Exp: 1+ years in clinical lab work |
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.Maintains laboratory in a clean, functional state, as well as cleaning, performing or scheduling equipment and instrument maintenance/calibration/certification, as required | 7/18/2020 |
| 1068 | Ginkgo Bioworks Boston, MA Production Operations Engineer Assocites in computer science, engineering or related Exp: 1 year in network/production support |
Provide front-end support for our high-complexity CLIA laboratory. Establish root causes of application errors, escalating serious concerns to engineering team members and ensuring issue resolution. Actively participate in post mortem discussions. Manage detailed records of configuration changes | 7/18/2020 |
| 1069 | Ginkgo Bioworks Boston, MA High-Throughput Screening Research Associate BS or MS in biological/chemical sciences or engineering Exp: 1-3 years research experience |
We’re looking for highly talented and motivated research associates to join our high-throughput screening (HTS) team and help carry out these critical functions. High-throughput culturing of microbial strains using a variety of automated solutions for use in high-throughput screens. Creation of strain libraries through the execution of a HTP transformation and colony picking workflows. | 7/18/2020 |
| 1070 | Ginkgo Bioworks Boston, MA Foundry Operations Engineer - Fermentation BS/BA Exp: 1+ year industry experience |
Execute fermentation processes across multiple Ginkgo organisms, with a focus on filamentous fungi, bacteria, and yeast as directed by senior engineers. Maintain responsibility for setup and breakdown of fermentation equipment. Aid in the preparation of media and other required reagents. Collect and process samples | 7/18/2020 |
| 1071 | Ginkgo Bioworks Boston, MA Build Engineer / Research Associate BS or MS in microbiology or genetics Exp: 1+ year in lab |
We are seeking inquisitive research associates to join our Build team to help us run and improve several high-throughput molecular biological processes. A demonstrated ability to evolve a process in response to changing technology and demands is essential. Experience in a mixed team of software developers, process engineers, and biologists is important. | 7/18/2020 |
| 1072 | GenapSys Redwood City, CA Research Associate, Development MS in molecular biology Exp: 1+ year in industry |
Help to define technical requirements for consumable products and generate data to support the specifications that are established and used for incoming QC. Participate on both short-term and long-term stability studies to establish high risk reagents, work flow and storage issues. Help to develop orthogonal analytical methods that can correlate with performance on our sequencing platform. | 7/18/2020 |
| 1073 | Genewiz Cambridge, MA Laboratory Technician I HS Diploma/GED Exp: 1+ year in lab |
Our Lab Techs strictly adhere to laboratory SOPs to ensure quality and safety and often communicate with our customers via email. They understand our customer needs with empathy and know that everything they do is making a difference. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. | 7/18/2020 |
| 1074 | Genewiz South Plainfield, NJ Associate Scientist I BS in biological sciences Exp: 1+ year in biological laab |
Prepare amplified template libraries for high-throughput sequencing. Carry out DNA sequencing on next-generation DNA analyzers. Perform routine maintenance of DNA analyzers and related equipment. Check inventory and replenish consumable sequencing supplies. Communicate with customers by phone and e-mail in a friendly and professional manner | 7/18/2020 |
| 1075 | Genewiz La Jolla, CA Laboratory Technician I HS Diploma/GED Exp: 1+ year in lab |
Our Lab Techs strictly adhere to laboratory SOPs to ensure quality and safety and often communicate with our customers via email. They understand our customer needs with empathy and know that everything they do is making a difference. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. | 7/18/2020 |
| 1076 | Neo Genomics Carlsbad, CA Laboratory Technician - Covid-19 Unit BS/BA in life sciences or engineering Exp: 0-2 years |
As a Laboratory Technician you will work under the direct supervision of licensed personnel to prepair Covid-19 samples for processing. You will assist with responsibilities associated with processing specimens for clinical testing and will provide general support for the laboratory following established policies and procedures. | 7/18/2020 |
| 1077 | Neo Genomics Ft. Myers, FL Clinical Laboratory Technologist I - Molecular- Tuesday -Saturday; Day Shift BS/BA in biological/chemical sciences Exp: 1+ year in clinical lab |
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. | 7/18/2020 |
| 1078 | Neo Genomics Carlsbad, CA Clinical Laboratory Technologist -Covid-19 Testing Unit BS/BA in biological/chemical sciences Exp: 1+ year in clinical lab |
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. | 7/18/2020 |
| 1079 | Neo Genomics Carlsbad, CA Clinical Laboratory Technologist - Covid-19 Unit BS/BA in biological/chemical sciences Exp: 1+ year in clinical lab |
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. Documents all corrective actions taken when test systems deviate from the laboratory’s established performance specifications | 7/18/2020 |
| 1080 | Ginkgo Bioworks Boston, MA Research Associate, Protein Engineering BS or MS in biological sciences or engineering Exp: 1+ years in industry working with enzymes |
The protein engineering team works to address the complex challenges of enzyme discovery, characterization, and engineering. We utilize state-of-the-art computational software developed at Ginkgo to discover novel enzymes and employ cutting-edge software like Rosetta for rationally designing improvements. We want a person who is eager to learn and has a desire to utilize automation to work more efficiently | 7/18/2020 |
| 1081 | Genentech Hillsoboro, OR QC Lab Technician (Contract) AA degree in sciences Exp: 1 year in related |
Perform routine and semi-routine work that supports QC operations. Sampling and testing of utility systems (Color, Appearance, Odor, TOC, Conductivity, Bioburden, Endotoxin, Particulates and Moisture), facility monitoring (viable monitoring plates and non-viable particulate). Share maintenance responsibilities with other laboratory personnel such as reagent preparation, media growth promotion, and cleaning of incubators and biosafety cabinets. | 7/18/2020 |
| 1082 | Genentech Vacaville, CA Manufacturing Technician - BioProcess BS/BA in life sciences or engineering Exp: 0-2 years |
The Manufacturing Technician is responsible for producing innovative bio-therapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment. The individual will be required to work in and maintain a clean room environment. Area of work must remain in a high state of inspection readiness at all times. | 7/18/2020 |
| 1083 | Genentech South San Francisco, CA PV Clinical Associate Health Care degree Exp: 0-2 years clinical experience |
Completes drug safety monitoring and tracking in a timely, thorough and accurate manner in accordance with pharmacovigilance (PV) and related standards, regulations and Genentech/Roche Standard Operating Procedures (SOPs). Reviews, evaluates and verifies potential AE information during Preliminary Assessment (PA) to determine required action per internal policies and procedures and perform data entry of adverse event by timely completion of the case via Roche global safety database. Performs seriousness / validity / causality and conducts quality review of all cases (as applicable) based on their medical assessment | 7/18/2020 |
| 1084 | Zynex Medical Champaign, IL Medical Device Sales - Addressing the Opioid Crisis BS/BA Exp: 1-3 year(s) |
Zynex is seeking college graduates or individuals with 1-3 years of outside sales experience in either B2B or medical device sales. Must be a self-starter, resourceful, assertive, and organized with a proven track record of documented sales success. This is an opportunity to build your own prescription-based business. Call points include: Pain Management doctors, Orthopedic groups and Physical Therapy clinics for our NexWave and other DME devices that offer an alternative to opioid pain medication. This is an autonomous sales position that requires you to be independent and dedicated to becoming a top medical device sales representative. You must be able to build trusting relationships quickly and possess the drive to accomplish goals on a weekly basis. etc. | 7/15/2020 |
| 1085 | Zynex Medical Carbondale, IL Medical Device Sales - Addressing the Opioid Crisis BS/BA Exp: 1-3 year(s) |
Zynex is seeking college graduates or individuals with 1-3 years of outside sales experience in either B2B or medical device sales. Must be a self-starter, resourceful, assertive, and organized with a proven track record of documented sales success. This is an opportunity to build your own prescription-based business. Call points include: Pain Management doctors, Orthopedic groups and Physical Therapy clinics for our NexWave and other DME devices that offer an alternative to opioid pain medication. This is an autonomous sales position that requires you to be independent and dedicated to becoming a top medical device sales representative. You must be able to build trusting relationships quickly and possess the drive to accomplish goals on a weekly basis. etc. | 7/15/2020 |
| 1086 | Zynex Medical Olney, IL Medical Device Sales - Addressing the Opioid Crisis BS/BA Exp: 1-3 year(s) |
Zynex is seeking college graduates or individuals with 1-3 years of outside sales experience in either B2B or medical device sales. Must be a self-starter, resourceful, assertive, and organized with a proven track record of documented sales success. This is an opportunity to build your own prescription-based business. Call points include: Pain Management doctors, Orthopedic groups and Physical Therapy clinics for our NexWave and other DME devices that offer an alternative to opioid pain medication. This is an autonomous sales position that requires you to be independent and dedicated to becoming a top medical device sales representative. You must be able to build trusting relationships quickly and possess the drive to accomplish goals on a weekly basis. etc. | 7/15/2020 |
| 1087 | Zynex Medical Bismarck, ND Medical Device Sales - Addressing the Opioid Crisis BS/BA Exp: 1-3 year(s) |
Zynex is seeking college graduates or individuals with 1-3 years of outside sales experience in either B2B or medical device sales. Must be a self-starter, resourceful, assertive, and organized with a proven track record of documented sales success. This is an opportunity to build your own prescription-based business. Call points include: Pain Management doctors, Orthopedic groups and Physical Therapy clinics for our NexWave and other DME devices that offer an alternative to opioid pain medication. This is an autonomous sales position that requires you to be independent and dedicated to becoming a top medical device sales representative. You must be able to build trusting relationships quickly and possess the drive to accomplish goals on a weekly basis. etc. | 7/15/2020 |
| 1088 | Zynex Medical Burlington, VT Medical Device Sales - Addressing the Opioid Crisis BS/BA Exp: 1-3 year(s) |
Zynex is seeking college graduates or individuals with 1-3 years of outside sales experience in either B2B or medical device sales. Must be a self-starter, resourceful, assertive, and organized with a proven track record of documented sales success. This is an opportunity to build your own prescription-based business. Call points include: Pain Management doctors, Orthopedic groups and Physical Therapy clinics for our NexWave and other DME devices that offer an alternative to opioid pain medication. This is an autonomous sales position that requires you to be independent and dedicated to becoming a top medical device sales representative. You must be able to build trusting relationships quickly and possess the drive to accomplish goals on a weekly basis. etc. | 7/15/2020 |
| 1089 | Zynex Medical Jonesboro, AR Medical Device Sales - Addressing the Opioid Crisis BS/BA Exp: 1-3 year(s) |
Zynex is seeking college graduates or individuals with 1-3 years of outside sales experience in either B2B or medical device sales. Must be a self-starter, resourceful, assertive, and organized with a proven track record of documented sales success. This is an opportunity to build your own prescription-based business. Call points include: Pain Management doctors, Orthopedic groups and Physical Therapy clinics for our NexWave and other DME devices that offer an alternative to opioid pain medication. This is an autonomous sales position that requires you to be independent and dedicated to becoming a top medical device sales representative. You must be able to build trusting relationships quickly and possess the drive to accomplish goals on a weekly basis. etc. | 7/15/2020 |
| 1090 | Zynex Medical Dallas, TX Medical Device Sales - Addressing the Opioid Crisis BS/BA Exp: 1-3 year(s) |
Zynex is seeking college graduates or individuals with 1-3 years of outside sales experience in either B2B or medical device sales. Must be a self-starter, resourceful, assertive, and organized with a proven track record of documented sales success. This is an opportunity to build your own prescription-based business. Call points include: Pain Management doctors, Orthopedic groups and Physical Therapy clinics for our NexWave and other DME devices that offer an alternative to opioid pain medication. This is an autonomous sales position that requires you to be independent and dedicated to becoming a top medical device sales representative. You must be able to build trusting relationships quickly and possess the drive to accomplish goals on a weekly basis. etc. | 7/15/2020 |
| 1091 | 10x Genomics Pleasanton, CA Research Associate 2-Molecular Biology/Product Development MS in molecular biology, biochemistry, genetics or related Exp: 1+ year(s) |
We are seeking an outstanding Research Associate to join the Product Development group to support the development and commercial launch of new products. This is a unique cross-disciplinary position that will work closely with a variety of groups including Molecular Biology, Chemistry, Microfluidics, QC, and Manufacturing, to develop and validate novel reagents for the rapid expansion of 10x product lines. Candidates must have a broad working knowledge of molecular biology and be able to apply that knowledge creatively and independently in a fast-paced work environment. The successful applicant will have exceptional attention to detail and the ability to meticulously execute and analyze highly complex experiments. Previous industry experience is essential. etc. | 7/15/2020 |
| 1092 | 3T Biosciences South San Francisco, CA Research Associate, Protein Engineering MS Exp: 0-2+ year(s) |
Your Typical Responsibilities: Protein engineering to support TCR-T cell programs, and identify compounds with optimal therapeutic index. TCR engineering for improved efficacy, and specificity. Performing cell-based assays to test prospective optimized leads. Discovery of TCR mimetic (mTCR) compounds that bind selectively to pMHC targets identified at 3T. Improvement of existing yeast display platforms and development of next-generation pMHC libraries. etc. | 7/15/2020 |
| 1093 | Abbot Menlo Park, CA Assembler I - SECOND SHIFT HS diploma or equivalent Exp: 0-3 years |
Position Summary: Performs a wide variety of electronic, mechanical, or electro-mechanical assembly operations on assemblies or sub-assemblies. Sets up and operates automatic or semi-automatic machines. May perform other tasks including, but not limited to; placing labels on packages, and putting data sheets with product. Main Responsibilities: Assembles, repairs, inspect and/or test products following written instructions. Ability to read and comprehend basic instructions and other work related documents, written in English. Sets up and operates a variety of manufacturing machines or equipment following written instructions in the English language. etc. | 7/15/2020 |
| 1094 | Abbot Sylmar, CA Mechanical Development Quality Engineer I BS/MS in mechanical, system, or industrial engineering or related Exp: 0-2 years |
Analyze quality standards for components, materials or services. Apply measures, sampling methods, testing methodology and other procedures that ensure that quality standards are met. We are seeking an experienced, high caliber Mechanical Development Quality Engineer to assure new or modified products conform to quality standards and establish 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. Employees act on their strong desire to make a difference, partner with others and put ideas into action. Employees are engaged by a work culture that is team-oriented, fast paced and progressive. etc. | 7/15/2020 |
| 1095 | Abbot Plymouth, MN Analyst II, Product Surveillance BS in a healthcare, science or technical field Exp: Not necessary for BS candidates |
Postmarket Surveillance Analyst may perform two different functions within complaint handling. One role is that of complaint investigation management which includes all activities pertaining to receiving and investigating reports of worldwide complaints/events on a variety of products; entering information into the complaint database; independently determining and filing appropriate medical devices reports with various regulatory agencies; participating on cross-functional teams; and providing information on product complaints to various teams (e.g. Regulatory, Quality Engineering). The other role of the Postmarket Surveillance Analyst is performing evaluations on various types of returned complaint products (e.g. disposable and implantable products, electronic and electro-mechanical medical devices and systems) such as performing non-destructive and destructive testing; reviewing of Device History Records; etc. | 7/15/2020 |
| 1096 | Abbot Scarborough, ME Production Specialist II HS diploma or equivalent Exp: 1+ year(s) |
We have an exciting opportunity for a Production Specialist II within our Abbott Rapid Diagnostics business located at Scarborough, Maine. In this role, you will perform the work required for the assembly of components, devices, and/or the final product depending on the trade assigned. Abbott Rapid Diagnostics (formerly Alere) is part of Abbott’s Diagnostics family of businesses, bringing together exceptional teams of experts and industry-leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions. RESPONSIBILITIES: Performs work required for the assembly of components, devices and/or the final product. Performs routine work in all production areas with limited supervision. etc. | 7/15/2020 |
| 1097 | Abbvie Cambridge, MA Associate Scientist II/Scientist I, In Vivo Pharmacology MS in biology or related Exp: 0+ years |
AbbVie is seeking an experienced, hands-on in-vivo scientist to join the In Vivo Pharmacology team at the Cambridge Research Center in Cambridge, MA. This individual will be responsible for designing and executing in vivo studies to support Parkinson’s Disease drug discovery projects. Key Responsibilities: Working closely with team members to design and execute in vivo experiments to support drug discovery efforts including target identification, target validation and efficacy of novel molecules. Developing new technologies and methods to understand disease pathophysiology and target biology. Responsible for implementation of in vivo studies and data collection as well as interpretation/analysis and presentation of results as needed. etc. | 7/15/2020 |
| 1098 | Abcam Eugene, OR Research Associate, Quality Control BS in biology or related Exp: 1+ year(s) |
We are seeking a Research Associate for our Quality Control team to test a wide variety of antibody-based products in our Eugene, OR facility. The core responsibility will be to provide support to the quality control team by testing our catalog of products after they have completed the manufacturing process. These products include quantity ELISA kits, activity ELISA kits, Western blot antibodies, immunocytochemistry antibodies, and flow cytometry kits. Primary Responsibilities: Perform documented methods required for finished product quality testing. Review manufacturing documentation for process deviations. Communicate analyzed results in detailed written reports. etc. | 7/15/2020 |
| 1099 | Abcam Burlingame, CA Manufacturing Associate Unspecified Exp: Entry level |
The successful candidate will undertake training in all procedures and work in compliance with Good Manufacturing Practices (GMP) defined under our Quality System Regulations and ISO13485 accreditations. In summary, the successful candidate will; Dilute and test antibody reagents for performance in immunohistochemical staining of tissues, according to approved procedures. Aliquot and package finished goods. Document test procedures, organize data and maintain accurate records of work performed according to GMP, QSR and ISO13485. Complete and review batch production records to provide cGMP documentation. Undertake stock-taking. etc. | 7/15/2020 |
| 1100 | Abzena Bristol, PA Bioconjugation Scientist MS in biochemistry, chemistry, protein chemistry or related Exp: 1-5+ year(s) |
Responsible for contributing to the optimization and development of bioconjugation techniques and related processes, including but not limited to the areas of Antibody Drug Conjugates (ADCs), protein drug conjugates, conjugated vaccine, Fluorescent-Probe Bioconjugation and Protein-Protein cross-linking. Typical Duties Include: Planning of synthetic routes/strategies, the execution and delivery of bioconjugation projects for Abzena’s clients. Preparation, purification and characterization of all materials including the protein and the drug molecules. Maintaining clear and current records of their work within a laboratory notebook and performing all applicable analytical work. etc. | 7/15/2020 |
| 1101 | Absorption Systems Exton, PA Associate Scientist / Scientist – Molecular or Immunology BS/MS Exp: 1-3 year(s) |
Absorption Systems, provides analytical support for gene and cell therapy products through every stage of development, is seeking a candidate for either an Associate Scientist position in molecular biology and gene expression at the headquarter location in Exton, Pennsylvania. Absorption Systems also provides non-clinical testing services to pharmaceutical and biotech companies to support research and development of drugs, biologics, and medical devices. Primary Responsibilities: Preparation for protocol of assay, planning and conducting experiments under the direction of a senior scientist. Conducting studies on molecular biology assays, such as purification of DNA/RNA/Protein from samples, qPCR, protein assays. etc. | 7/15/2020 |
| 1102 | Wuxi AppTec King of Prussia, PA Associate Scientist Downstream Process Development MS in biology, biochemistry, immunology, bioengineering or related Exp: 0-2 years |
The successful candidate will be responsible for conducting experiments to support client-based processes with a focus on vaccine Downstream cell culture processes. This position will work with a team of scientists and technical specialists responsible for process development and technology transfer to ensure the application of well-designed unit operations for inclusion in routine manufacturing operations supplying clinical and commercial materials. Contributes to operations of development team, and may support tech transfer activities as necessary. Responsibilities: Work according to defined protocols on defined biopharmaceutical projects for development and/or characterization of vaccine downstream manufacturing processes. Execute lab-scale experiment in supporting downstream process development, verification, characterization. etc. | 7/14/2020 |
| 1103 | Wuxi AppTec Philadelphia, PA Manufacturing Associate I AS/BS 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). Responsibilities: Understands aseptic technique concepts. Thorough understanding of Good Laboratory Practices and Good Manufacturing Practices. Able to operate and maintain equipment. Performs solution and material preparation. Possesses basic technical knowledge and background. etc. | 7/14/2020 |
| 1104 | Wuxi AppTec San Diego, CA Research Associate I BS in biology Exp: 0-1 year(s) |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology Division. We’re seeking a highly motivated Research Associate I to join the team. Responsibilities: Assist with in vivo pharmacology experiments for preclinical contract research. Perform in vivo studies to evaluate anti-cancer efficacy of test agents in tumor mouse models with supervision. Monitor mouse groups enrolled in drug efficacy, mechanism of action, PKPD and proof-of-concept studies. Perform drug dosing by various routes of administration. Perform in-life blood sampling through various routes. etc. | 7/14/2020 |
| 1105 | Wuxi AppTec San Diego, CA Research Associate II AS/BS in biology Exp: 1-3 year(s) |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology Division. We’re seeking highly skilled and motivated Research Associate to join the team. Responsibilities: Conducting in vivo pharmacology experiments for preclinical contract research with minimal supervision. 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. | 7/14/2020 |
| 1106 | X-Chem Pharmaceuticals Waltham, MA Research Associate / Senior Research Associate BS/MS in biochemistry, chemistry, or related Exp: 1-3 year(s) |
X-Chem Pharmaceuticals is seeking candidates for the position of Research Associate / Senior Research Associate, Lead Discovery. 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. Key Responsibilities: Determine suitability of constructs for affinity-mediated discovery processes. Use X-Chem’s DNA-Encoded Chemical Library technology to support a range of external projects. Assist in the interpretation of selection output data. Communicate observations, interpretations and conclusions internally and externally. etc. | 7/14/2020 |
| 1107 | Xellia Pharmaceuticals Cleveland, OH Aseptic Operator, IV Bag Manufacturing I HS diploma or equivalent Exp: 0-1 year(s) |
The contents contained in this job description are the minimum requirements required to be met for the aforementioned position. Under the direction of area management or designee, the Aseptic Operator I is responsible for performing all necessary tasks both in and outside of the classified manufacturing suites in support of manufacture of safe and effective sterile (injectable) pharmaceutical products at the Xellia Cleveland plant. Key Responsibilities: Perform job functions with in compliance of 21CFR part 210 and 211, FDA, OSHA and other regulatory agencies. Ensure that the current requirements for Environmental, Health, Safety (EHS) issues are met within the production operations. Ensure training compliance for assigned curriculum prior to performing any work task. Set-up, Operation, and troubleshooting of key manufacturing equipment: including (but not limited to) lyophilizer, autoclave, parts washers, filler, capper, CIP/SIP skid, etc. | 7/14/2020 |
| 1108 | Xellia Pharmaceuticals Cleveland, OH Inside Sales Representative - Southwest Territory (Remote) BS/BA Exp: 1-3 year(s) |
As a part of Xellia’s growing, energetic, and innovative pharmacy injectables sales seam, the Digital Sales Representative is responsible for driving sales to new customers while meeting established individual and organizational sales objectives. You will build and maintain valuable sales skills, cross-functionally learn about all facets of the business and help develop a pathway for growth opportunities and career advancement. Key Responsibilities: Manage, prospect, and build relationships within an assigned territory to drive new business, increase revenue growth and ensure customer satisfaction. Manage a sales pipeline, sales activity, and monthly business forecasting through customer interfacing activities and sales data analysis. Present regular updates to the Management team. etc. As a part of Xellia’s growing, energetic, and innovative pharmacy injectables sales seam, the Digital Sales Representative is responsible for driving sales to new customers while meeting established individual and organizational sales objectives. You will build and maintain valuable sales skills, cross-functionally learn about all facets of the business and help develop a pathway for growth opportunities and career advancement. Key Responsibilities: Manage, prospect, and build relationships within an assigned territory to drive new business, increase revenue growth and ensure customer satisfaction. Manage a sales pipeline, sales activity, and monthly business forecasting through customer interfacing activities and sales data analysis. Present regular updates to the Management team. etc. | 7/14/2020 |
| 1109 | Xellia Pharmaceuticals Cleveland, OH Aseptic Operator II - 12 Hour Shift HS diploma or equivalent Exp: 1-2 year(s) |
The contents contained in this job description are the minimum requirements required to be met for the aforementioned position. Under the direction of area management or designee, the Aseptic Operator II is responsible for performing all necessary tasks both in and outside of the classified manufacturing suites in support of manufacture of safe and effective sterile (injectable) pharmaceutical products at the Xellia Cleveland plant. Key Responsibilities: Perform job functions with in compliance of 21CFR part 210 and 211, FDA, OSHA and other regulatory agencies. Ensure that the current requirements for Environmental, Health, Safety (EHS) issues are met within the production operations. Ensure training compliance for assigned curriculum prior to performing any work task. Set-up, Operation, and troubleshooting of key manufacturing equipment: including (but not limited to) lyophilizer, autoclave, parts washers, filler, capper, CIP/SIP skid, etc. Documentation of perform tasks as per established Good Documentation Practices, and review of executed documentation (batch records, logbooks, etc.) in a timely manner. etc. | 7/14/2020 |
| 1110 | Xellia Pharmaceuticals Cleveland, OH Inside Sales Representative - Midwest Territory (Remote) BS/BA Exp: 1-3 year(s) |
As a part of Xellia’s growing, energetic, and innovative pharmacy injectables sales seam, the Digital Sales Representative is responsible for driving sales to new customers while meeting established individual and organizational sales objectives. You will build and maintain valuable sales skills, cross-functionally learn about all facets of the business and help develop a pathway for growth opportunities and career advancement. Key Responsibilities: Manage, prospect, and build relationships within an assigned territory to drive new business, increase revenue growth and ensure customer satisfaction. Manage a sales pipeline, sales activity, and monthly business forecasting through customer interfacing activities and sales data analysis. Present regular updates to the Management team. etc. | 7/14/2020 |
| 1111 | Xencor Monrovia, CA Laboratory Assistant BS/BA Exp: Entry level |
The Lab Assistant, Cell Biology is a temporary role in our Research facilities. Ours is a collaborative, agile environment requiring a sense of urgency, excellent work ethic and the ability to work efficiently and accurately. Responsibilities: Tissues culture with sterile technique. Experience with primary tissues and cell lines. Work with Peripheral Blood Mononuclear Cell (PBMC) is a plus. Maintain lab supplies. | 7/14/2020 |
| 1112 | Xeris Pharmaceutical Chicago, IL Desktop Support Technician (Temp to Hire) AS/AA in information technology or related Exp: 1-2 year(s) |
The Desktop Support Technician is responsible for supporting the organization’s end users via phone, email, and in person, in a dynamic, fast-paced environment. Strong customer service skills are a key component of this position which requires excellent communication and interpersonal skills, as well as the ability to resolve problems. Support may include but is not limited to hardware troubleshooting, software installations and/or configuration, imaging and deploying laptops/desktops, break/fix troubleshooting and end user education. This position will also require the ability to recognize root cause issues and document, resolve or escalate the root cause problem as necessary for resolution. The position will also require various other assigned tasks and responsibilities to be carried out as new projects and changes in the infrastructure occur. etc. | 7/14/2020 |
| 1113 | Yokogawa West Valley City, UT Service Project Engineer BS in computers and electronics, instrumentation technology, or related Exp: 1-3 year(s) |
Yokogawa is seeking to hire a Service Project Engineer. PRIMARY TASKS: Successfully execute multiple, small to moderate projects to the defined scope, within budget, on schedule, and to the satisfaction of the customer (internal and external). Conducts systems operational test. Installs system hardware/software upgrades as required. Manage and review the drawing package ACAD documentation. Review vendor submittals, prepare factory and other purchase orders, track orders, and receive materials per the project schedule and scope. Troubleshoot existing systems on-line and support network / subsystem testing. Provide regular updates on work in progress, immediate notification of issues related to quality, cost, or schedule, and propose solutions as problems arise. etc. | 7/14/2020 |
| 1114 | Yokogawa Newman, GA Assembler II HS diploma or equivalent Exp: 1-5 year(s) |
Description: Produce units based on an hourly production. Determine type of unit, parts necessary and production procedures to be followed for the required unit model by reading shop orders, Tokochu and work tags. Assemble instrument per established production procedures by using a variety of electric tools, gauges and hand tools. Accurately completes the needed data on all check sheets or any other required information. Maintain high quality level by using proper assembly and testing techniques. Carry out duties under NYPS system making suggestions and learning all process. Maintain a clean work area by continuous monitoring of assigned station. Must have high level of dexterity to perform with accuracy in producing required quantities of product, with emphasis in quality. etc. | 7/14/2020 |
| 1115 | Zoetis Eagle Grove, IA Production Operator HS diploma or equivalent Exp: 6+ months |
This position is responsible for operating process equipment and following all site operating, Quality, cGMP, and safety procedures associated with manufacturing of bulk medicated feed additives (MFA) from raw material to finished product. Incumbent must be able to clearly and frequently communicate with various functions within the site, including production, maintenance, quality operations, fermentation development, and administration. This is a 3rd shift position for the hours of 10:00 pm – 6:00 am. POSITION RESPONSIBILITIES: Selects and weighs components in accordance with established manufacturing directions (batch records). Selects and moves components to weighing area or dumping station. Examines finished products to determine consistency and blend characteristics. Samples products according to Quality Control procedures. Selects and records lot number and weights of all materials, reconciles weights and yields on batch formulation sheet. etc. | 7/14/2020 |
| 1116 | Zoetis Charles City, IA Refrigeration Specialist AS/AA in refrigeration, electricity, climate control or electronics Exp: 0-3 years |
Maintains, repairs and troubleshoots business operations objects which include and not limited to: Freeze dryers, Coolers, Freezers, Ultra low freezers, Chillers, HVAC units, Utilities equipment, Electrical systems, etc. Refrigeration Technician – Incumbents with refrigeration experience, use of tools and equipment and a wide variety of practices and procedures. As experience and competence is gained, assignments become more varied and are performed with greater independence. This class is flexibly-staffed with Refrigeration Technicians and incumbents may advance to the higher level after gaining the multi skills and experience which meet the qualifications for and demonstrating the ability to perform the work of the higher level class. etc. | 7/14/2020 |
| 1117 | Zoetis Charles City, IA Technical Process Specialist MS in microbiology, biological systems engineering, mechanical engineering or related Exp: 0-2 years |
Provide technical guidance on issues/projects within Manufacturing or Quality. Coordinate the engagement of the Global Manufacturing Technology (GMT) organization as needed. Identify and drive continuous process improvements. Lead large scale investigations for the site. Identify and implement cost savings initiatives for the site. Conducts all activities and makes decisions that are in accordance with Company policies & SOPs, Zoetis Values, & global regulatory guidelines (including cGMP/cGLP/cGCP), environmental guidelines, as appropriate, etc. Position Responsibilities: Take the manufacturing/quality lead in the introduction of new processes or modifications to existing processes as supported by Global Manufacturing Technology (GMT). Assist in performing technical evaluations and implementation of GMT initiatives to ensure robust process improvements and transfers. etc. | 7/14/2020 |
| 1118 | Zoetis Lincoln, NE Animal Laboratory Technologist HS diploma or equivalent Exp: 0-4+ years |
This position will support manufacturing in vivo potency and safety testing for product release, manufacturing investigations, and clinical research. The incumbent’s responsibility includes performing in vivo testing procedures, data collection, data audits, data entry/verification, some general care and husbandry of laboratory animals, performing test method investigations and assisting with research studies. Position Responsibilities: Perform routine laboratory testing. Test set-up / data audit/ data validation. Proficient with all injections [vaccinations / inoculations (IM, SQ, IP, ICr, IV), treatments (IM, SQ, orally, IV, topically)] and blood collections by all routes, as directed. Proficient with challenge techniques and post-challenge observations. Maintain required documentation for laboratory animal procedures (i.e. ACUPs, LIMS, SOPs). Assist with/perform laboratory animal testing associated with projects. Assist with trouble shooting and problem solving for assays and processes. etc. | 7/14/2020 |
| 1119 | Zoetis Lincoln, NE Packaging Technician – 2nd Shift HS diploma or equivalent Exp: 1-2 year(s) |
Work as part of a team operating pharmaceutical packaging lines. Operate packaging equipment and other related tasks. Maintain accurate and concurrent documentation of all tasks completed. Maintain a positive attitude and be able to work well with others in a team environment. Demonstrate good attendance. Position Responsibilities: Record Keeping and Documentation: Maintain and complete accurate records (time cards, batch records, log books, etc.). Equipment: Operate assigned equipment, i.e. . PLC controlled packaging line, vision system, etc. Clean production equipment and facilities. Set-up/ disassemble production equipment. Operate specific in-process devices associated with the equipment, i.e. moisture analyzers, pH meters, etc. | 7/14/2020 |
| 1120 | Zoetis Lincoln, NE Packaging Technician HS diploma or equivalent Exp: 6 months |
Position Responsibilities: Working with a coach and / or trainer complete the Packaging Operations On the Job Training Program which includes, but is not limited to the following: Complete Training Modules (Packaging Orientation, Packaging Safety, Packaging Safety Program, Packaging Colleague Expectations, and the department specific module for the packaging area assigned). Complete job specific training check lists for 5 packaging lines. Learn to use Packaging related Standard Operating Procedures, Batch Records, Log Books and Job Aides. Learn the operation of Motorized Materials Handling Equipment as assigned. Learn to identify packaging component and finished goods quality expectations. Learn to complete product specific packaging documents and log book entries. Learn the support of manufacturing departments through the movement of product, raw materials, and supplies in and out of the manufacturing areas. etc. | 7/14/2020 |
| 1121 | Zoetis Kalamazoo, MI Formulation Scientist MS in pharmacy, pharmaceutics, chemical engineering or related Exp: 0-5 years |
We are seeking formulation scientist to support development of new veterinary drug products and reformulation of existing products. The formulation scientist will be responsible for characterization of candidate molecules for the development of appropriate dosage forms for clinical and commercial needs. This is an exciting opportunity where scientist will have full ownership on formulation research in early stages as well as often late stage development. The scientist will be expected to support interdisciplinary teams of colleagues from Discovery, clinical development, safety, regulatory, marketing and global manufacturing, with technical expertise. On occasion, the scientist will be expected to lead PharSci team and bring forward the drug product, analytical methods and drug supplies for drug candidates from early discovery stage to commercialization. Working on veterinary medicine, the scientist will have opportunity to work on the development of oral, topical, parenteral and other delivery routes. etc. | 7/14/2020 |
| 1122 | Zymergen San Francisco, CA Chemistry Associate, Consumer Care MS in chemistry, chemical engineering, material science or related Exp: 1-2 year(s) |
Zymergen is looking for a Chemistry Associate with training and experience in Personal Care. The candidate will be a key contributor to the formulation efforts. The candidate will work closely with the project scientists to help drive the overall program progress on a technical level. Job Description: Experience in preparing lab batches and optimizing Home and Personal Care formulations under the scientist’s guidance. Experience in using rheometer to measure shear viscosity and tribology for understanding sensory attributes. If no experience in rheometer, passionate about learning how to use a rheometer. Carry out material characterisation such as pH, playtime, hydration, surface roughness and color change by X-rite, SPF, and viscometry. Document data entry of materials characterisation, pricing, formulations and SOPs. etc. | 7/14/2020 |
| 1123 | Wuxi AppTec San Diego, CA Research Associate I AS/BS in biology Exp: 0-1 year(s) |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology Division. We’re seeking a highly motivated Research Associate I to join the team. Responsibilities: Assist with in vivo pharmacology experiments for preclinical contract research. Perform in vivo studies to evaluate anti-cancer efficacy of test agents in tumor mouse models with supervision. Monitor mouse groups enrolled in drug efficacy, mechanism of action, PKPD and proof-of-concept studies. Perform drug dosing by various routes of administration. Perform in-life blood sampling through various routes. etc. | 7/14/2020 |
| 1124 | Fresenius Kabi Wilson, NC QC TECHNICIAN II BS/BA in chemistry Exp: 1-2 years lab experience |
Responsibilities include routine testing to support product release, raw material release, and cleaning verification. The technician will rely on experience and judgment in order to plan and accomplish goals. Routine testing of samples supporting incoming raw materials, in-process production, finished product, and validation. Utilize LIMS for data entry and test recording | 7/12/2020 |
| 1125 | Fresenius Kabi Lake Zurich, IL ASSOCIATE ELECTRONIC SUBMISSIONS SPECIALIST BS/BA Exp: 0-2 years in pharma |
Responsible for the electronic compilation and publishing of the company’s submissions to global drug, biological, and device regulatory authorities. Reporting to a Manager in Regulatory Affairs (RA), the position is responsible for the compilation and publishing of submissions to regulatory agencies. The position works with Plant and Corporate RA Specialists to obtain required documents. | 7/12/2020 |
| 1126 | Fresenius Kabi Grand Island, NY QC TECHNICIAN II - 1st Shift F,S,S,M Associates or BS/BA Exp: AS: 1-2 years, BS: 0 years |
This individual holding the position of QC Technician II shall be responsible for performing routine testing of in-process and finished product samples, raw material, stability, and utilities. They shall be responsible for monitoring the environmental conditions in the laboratory and in manufacturing areas. They shall support validation projects. This position must be available to work overtime as assigned. | 7/12/2020 |
| 1127 | Fresenius Kabi Canton, MA MANUFACTURING TECHNICIAN I (2nd shift) HS Diploma/GED Exp: 0-2 years industry experience |
Key Accountabilities include: Execution of routine production operations, labeling, quality control, inventory management, continuous improvement, maintenance of clean room equipment, carry out work in a safe manner while notifying management of safety issues and risks, assumes other duties and responsibilities as directed by supervisor. | 7/12/2020 |
| 1128 | Fresenius Kabi Grand Island, NY ASSOCIATE SCIENTIST - 1st Shift BS/BA or higher Exp: 1 or more years related experience |
Performs Method Transfers/method verifications/Co-Validations of testing procedures utilized within the Quality Control Laboratory. Prepares testing documentation or progress reports on projects and recommends course of future action. Acts as liaison between the Product Development, Stability, and the QC Chemistry Laboratories for the transfer and implementation of new procedures. | 7/12/2020 |
| 1129 | Fresenius Kabi Wilson, NC MANUFACTURING OPERATOR HS Diploma/GED Exp: 0-2 years |
Responsible for the daily coordination and sterilization of product. Performs Preventative Maintenance tasks on the terminal sterilizers. Responsible for sterilizer cycle review, troubleshooting of sterilizer problems, documentation of problems, and retrieval and delivery of product samples. Coordination with Maintenance personnel for repair of sterilizers. | 7/12/2020 |
| 1130 | Fresenius Kabi Grand Island, NY ASSOCIATE VALIDATION SCIENTIST BS/BA in sciences or engineering Exp: |
Responsible for providing technical support to operations in terms of equipment/system requalifications/ qualifications. Will perform studies as part of equipment improvement teams charged with enhancing the compliance and performance of plant systems, while considering the regulatory requirements for change control. Individual must also perform HEPA filter integrity/velocity testing and participates as hands-on work in critical area (class 100) airflow pattern testing. | 7/12/2020 |
| 1131 | Freudenberg Baldwin Park, CA Project Engineer I – Injection Molding BS/BA in engineering Exp: 1-2 years is engineering |
Work closely with project managers to gather/prepare all documentation relevant to a particular project. Responsible for Drafting and issuing validation protocols and production documents using information provided by customers and project managers. Responsible for gathering customer and technical information as required to make changes to documents or procedures at the customers request. | 7/12/2020 |
| 1132 | Freudenberg Carpinteria, CA Manufacturing Quality Engineer I BS in engineering or life sciences Exp: 1-3 years in regulated industry |
Responsible to provide Customer and Engineering feedback in regards to MSA, Critical to Quality Characteristics (CTQ’s) and Acceptance Activities. Lead Measurement System Analysis activities including Gage RnR, Test Method Validations, Test Procedures, etc. as part of the Design Transfer process. Provides all planning necessary to ensure effective product acceptance. This includes, but is not limited to, inspection instructions, equipment and gage requirements, and sampling plans. | 7/12/2020 |
| 1133 | Freudenberg Jeffersonville, IN Manufacturing Associate - 2nd Shift HS Diploma/GED Exp: 0 years |
Hand assemble manufactured medical components. Complete required documentation for work performed. Quality inspect work performed. Follow defined work procedures. Provide your suggestions and ideas of continuous improvements | 7/12/2020 |
| 1134 | Frontage Secaucus, NJ Lab Technician Medical Assistant certification Exp: 1-3 years in clinical research |
Develop a high level of familiarity and knowledge of the study protocol and flow chart of study procedures. Develop a strategy for implementing study procedures in compliance with study protocols. Performs laboratory procedures (g., preparation for admission testing, safety labs, and processing of biological specimen samples, shipment of samples and documentation of sample processing steps, etc.) as required by study protocol under the supervision of the Clinical Research Coordinator, Principal Investigator, and Sub-Investigators. | 7/12/2020 |
| 1135 | FujiFilm Diosynth Research Triangle park, NC Process Sciences Engineer II MS in biological or chemical sciences/engineering Exp: 0-4 years |
May support technical transfer of client project in and to manufacturing as applicable. Summarizes and report data. Interacts with supervisor and reports results and interpretation of experiments, project deliverables, and process readiness. Supports capital projects by providing technical expertise. Supports new project site-fit assessments as needed | 7/12/2020 |
| 1136 | FujiFilm Diosynth College Station, TX Validation Engineer I BS in engineering Exp: 0-2 years in validation |
Prepares and executes validation protocols. Prepares validation final report packages. Perform other duties as assigned | 7/12/2020 |
| 1137 | FujiFilm Diosynth College Station, TX Quality Control Analyst I Associates in chemistry or biochemistry Exp: 1-2 years in data review |
Review of QC analytical testing for GMP in-process, release and stability testing as needed: pH, Osmolality, Conductivity & qPCR, RP-HPLC, SEC, Agarose Gel Electrophoresis, UPLC, CE, IEF, Protein Purity Assays, Peptide Mapping, DNA Sequencing and/or UV/Vis Spectrometry preferred. Review technical transfer, qualification and validation protocols as needed. | 7/12/2020 |
| 1138 | FujiFilm Diosynth College Station, TX Microbiology Analyst I BS/BA or Associates in biology/chemistry Exp: 0-2 years |
Assist with QC microbiological aspects of cGMP compliance and testing. Assist manufacturing personnel in the identification of microbiological root cause analysis and provide technical advice as needed. Participate in the investigation and review of alert and action limit investigations as needed. Participate in cleaning and process validation activities involving microbiology. | 7/12/2020 |
| 1139 | FujiFilm Diosynth College Station, TX Downstream Manufacturing Technician I HS Diploma or Associates in biological sciences Exp: 0-1 years |
The Downstream Manufacturing Technician I will work directly with viral purification (either whole particle or split particle), continuous flow centrifuge operation, and sucrose gradient separation, techniques for filtration and chromatographic separation (i.e. column chromatography and HPLC) and viral inactivation. | 7/12/2020 |
| 1140 | FujiFilm Diosynth College Station, TX Cell Biology Analyst I BS in biology Exp: 0-2 years |
Assist with quality control analytical testing of samples provided to the QC laboratory. Assist with executing test qualification and validation of QC test methods. Writes and revises Standard Operating Procedures (SOPs) and other related Good Laboratory Practices (GLP)/Good Manufacturing Practices (GMP) documentation | 7/12/2020 |
| 1141 | FujiFilm Diosynth College Station, TX Automation Engineer BS in electrical/mechanical/chemical engineering Exp: 1 year |
Provide support on a daily basis to process control system, building management systems and data historian systems. Perform system software updates, security updates and upgrades to newer version. Support and enforce the data integrity program. Support and maintenance of computerized systems. Maintain Functional Specifications, Database Design Specifications and Hardware Design Specifications for automation systems. | 7/12/2020 |
| 1142 | Frontage Concord, OH Maintenance Technician HS Diploma/GED Exp: 1 year in facility services |
Assist in keeping building systems operational by completing assigned preventive maintenance requirements; following manufacturer’s instructions; troubleshooting malfunctions with oversight from supervisor and facilities staff. Assist in the maintenance and repair of various building equipment and systems including, but not limited to plumbing and piping systems, HVAC, electrical distribution, and boilers. | 7/12/2020 |
| 1143 | Eyevance Pharmaceuticals Fort Worth, TX Ophthalmic Territory Ranger BS/BA or equivalaent experience in sales/sciences Exp: 0-2 years |
Inside sales to white space and vacant territory business planning/support. Develop and maintain strong working relationships with target HCPs (via telephone, video conference and in person). Deliver approved, education-focused messages, as well as the assigned therapeutic area disease-state information to target HCPs (via telephone, video conference and in person). | 7/11/2020 |
| 1144 | Facet Medical Technologies Atlanta, GA Quality Engineer BS/BA in engineering or sciences Exp: 1-2 years in quality engineering |
The Quality Engineer plans and directs activities concerned with development, application, and maintenance of quality processes, materials, and products. Additionally, responsible for investigation manufacturing and customer nonconformance’s, determining root causes and corrective actions, reviewing and approving protocols and final reports and developing product specifications and sampling plans. | 7/11/2020 |
| 1145 | FHC Bowdoin, ME Product Development Engineer BS or better in biomedical, electrical or mechanical engineering Exp: 0-3 years |
The Product Development Engineer will contribute to all phases of product design, development and support. Technical competencies in the areas of biomedical engineering, electrical engineering and mechanical engineering are required. Maintain familiarity with relevant portions of the FHC Quality System and perform all duties within its guidelines, specifically those pertaining to design control, software development, EC’s and CAPA | 7/11/2020 |
| 1146 | FHC Bowdoin, ME Associate Manufacturing Engineer BS in engineering Exp: 0-2 years in process improvement |
The Associate Manufacturing Engineer works closely with Production, Quality, Materials and Engineering to help define and continually improve all manufacturing processes. This position will assist in resolving existing production issues, reviewing the existing process for improvement opportunities with regard to fixturing or other electrical/mechanical solutions, revising the process to ensure efficiency, and ensuring the process is accurately documented. | 7/11/2020 |
| 1147 | FHC Greenville, PA Production Technician HS Diploma/GED or Associates Exp: 0-2 years general experience |
The Production Technician assists FHC Greenville. This position involves some production duties, a variety of ERP System activities, and other general business office activities. Assemble product following work and print instructions as specified on manufacturing job orders generated from FHC’s ERP system. Relieve inventory physically and/or electronically through FHC’s ERP system if needed and follow the procedures to account for all items. | 7/11/2020 |
| 1148 | FHC Greenville, PA Manufacturing Support Specialist HS Diploma/GED or Associates Exp: 0-2 years general experience |
The Manufacturing Support Specialist assists GNS Production. This position involves some production duties, a variety of general accounting activities, and other general business office activities. Assists in performing secretarial, data entry and/or other general administrative tasks as required. Prepare and process Job order, Sales Orders. | 7/11/2020 |
| 1149 | Finch Cambridge, MA Clinical Assistant Certified medical assistant Exp: 1-2 years in health care |
A Clinical Assistant is responsible for a wide variety of clinical and clerical duties to support the Stool Donation program. The Clinical Assistant works under the general supervision of the Nursing and Supervising clinical staff is responsible for following Standard Operating Procedures to ensure the safety of stool donations. The Clinical Assistant will work collaboratively with donor operations staff and other departments to ensure strict adherence to standard operating procedures and maintain constant communication with clinical staff. | 7/11/2020 |
| 1150 | First Light Diagnostics Chelmsford, MA Research Technician Certification or AS in life sciences Exp: 1-2 years in life sciences research |
The Research Technician will work collaboratively with the research associates and scientists to support the development, verification, and validation of high performance immuno- and direct cell detection-based assays in preparation for FDA submission. S/he will manage laboratory inventory, ensure proper maintenance and calibration of laboratory equipment, and prepare common reagents used by the team. | 7/11/2020 |
| 1151 | Forma Therapeutics Watertown, MA Research Associate, Translational Science BS or MS in biology or realted Exp: 1-2 years in drug discovery/sciences |
Develop, optimize and perform assays using molecular biology procedures and technologies including qPCR, quantitative western blots, ELISA. In vitro culture of cancer cell lines and primary cells as well as DNA/RNA isolation from blood/tissue is required. Assist in the management of preclinical and clinical samples internally and with third party providers. | 7/11/2020 |
| 1152 | Foundation Medicine Cambridge, MA Bioinformatics Scientist I MS in biological/chemical/computer sciences Exp: 1+ years in industry or academic center |
The Scientist I, Bioinformatics develops novel methods for detecting, reporting and analyzing alterations in tumor DNA and RNA, while optimizing existing methods. The incumbent provides scientific and technical contributions for a designated project on an interdisciplinary team. The Scientist I, Bioinformatics is also responsible for supporting novel biomarker and companion diagnostics development by mining and analyzing various types of data generated during the product development and validation process. | 7/11/2020 |
| 1153 | Foundation Medicine Cambridge, MA Accessioning Technician II BS/BA in life sciences Exp: 0-1 years in CLIA lab |
The Accessioning Technician II performs critical sample receipt and data entry functions in FMI’s CLIA-certified clinical laboratory. Specifically, the Accessioning Technician II receives incoming samples and ensures that necessary information has been received to move forward with processing. The Accessioning Technician II is assigned to one of three shifts and may be assigned to work any day that the lab is operational. | 7/11/2020 |
| 1154 | Foxx Life Sciences Salem, NH WarehouseAssociate HS Diploma/GED or Associates Exp: 0-2 years, Entry Level |
Foxx Life Sciences is facing overwhelming demand for our products and is seeking entry-level, full-time, hourly WarehouseAssociates to assist with specific, daily functions within general manufacturing and assembly. There will be future possibilities for promotions as the company grows. All training is provided,and prior experience is not required for consideration. | 7/11/2020 |
| 1155 | Freenome South San Francisco, CA Clinical Laboratory Associate BS/BA in life sciences Exp: 1-2 years, knowledge of lab regulations |
Freenome’s Clinical Laboratory Associate will support the company’s Pre-Analytical Laboratory with the receiving, accessioning, plasma sample processing, and storage. Important to our mission is providing quality samples to process downstream for quality analysis and results.Verifies all aspects of incoming specimens and assess acceptability for testing | 7/11/2020 |
| 1156 | FreeThink Technologies Branford, CT Laboratory Scientist, Analytical Sciences BS or MS in chemistry or chemical engineering Exp: 1-2 years in pharma preferred |
Analyze products to determine chemical and physical properties following Company, client and Pharmacopeial methodologies with minimal supervision. Ensure all work performed is in compliance with standard operating procedures, good laboratory practices and good manufacturing practices. Document laboratory work concurrently in a clear, detailed and organized manner | 7/11/2020 |
| 1157 | Foundation Medicine Cambridge, MA CAPA Coordinator BS in related field Exp: 1-2 years in QA or medical/pharma |
The CAPA Coordinator assists with the CAPA System at FMI and supports with day to day administration of the CAPA process, documentation, and retention of the quality records. The Coordinator is responsible for expediting and coordinating a multitude of interrelated project activities pertaining to different daily tasks with changing priorities to ensure the successful completion of CAPA work stream. This position interacts with all departments within FMI. | 7/11/2020 |
| 1158 | Fate Therapeutics San Diego, CA Process Development Engineer, MSAT MS in biological or chemical sciences/engineering Exp: 1 year in biopharma |
The candidate will assist seniormembers of the MSAT teamin |