• Scientist I, Cell Culture, MSAT

    AbbVie (Worcester, MA)
    …+ A strong understanding and practical experience working in a cGMP -regulated biopharmaceutical environment + Proven experience working aseptically in cell culture ... processes. + Proven experience working at bench-top bioreactor scale. + Highly self-motivated with the ability to thrive in a fast-paced, collaborative team environment. Qualifications + Bachelor's Degree or equivalent education with typically 5 years of… more
    AbbVie (10/14/25)
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  • Quality Control Analyst I

    LGC Group (Milford, MA)
    …Procedures, as well as, regulatory agencies and customer requirements. + Comply with cGMP and ISO standards at all times to support LGC's commitment to Quality. ... + Assist with the implementation of corrective actions in response to internal and external audits. + Maintain the appearance of the QC lab on a daily basis for audit readiness. + Follow Operational Excellence principles, eg removal and disposal of expired… more
    LGC Group (10/13/25)
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  • Manufacturing Technician-2nd Shift

    Actalent (Milford, MA)
    …delivery systems (process skids). + Two plus years of experience in a cGMP manufacturing environment. Work Environment You will work in a GMP-based environment with ... an easygoing team that values camaraderie and teamwork. We balance having fun with getting the work done, creating an intimate setting where each employee can make a significant impact. Our innovative business serves numerous clients, offering exciting and… more
    Actalent (10/11/25)
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  • Manufacturing Technician

    Bio-Techne (Devens, MA)
    …to read and comprehend the English language. + Experience working in a cGMP /ISO facility a plus **Minimum Physical Requirements:** + Remain seated in a normal ... position for extended periods of time up to 8 hours + Walk, stand, and move for prolonged periods in a workday + Reach up and out with hands and arms + Talk and hear, verbally express information + Keyboard, 10 keys, + Repetitive motion; hands, arms + Lift up… more
    Bio-Techne (10/10/25)
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  • Chromatography Principal Scientist

    Sanofi Group (Cambridge, MA)
    …and trouble shoots + Knowledge of QbD concepts, specification setting, and cGMP , with experience in contributing to regulatory submission + Communicates effectively ... in individual and group settings and collaborate effectively in a multi-disciplinary team setting + Demonstrated project management skills + Consistent record of collaboration with scientists and other stakeholders at external enterprises + Advanced scientific… more
    Sanofi Group (10/10/25)
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  • Analytical Development Scientist

    Sanofi Group (Cambridge, MA)
    …and trouble shoots + Knowledge of QbD concepts, specification setting and cGMP + Communicates effectively in individual and group settings and collaborate ... effectively in a multi-disciplinary team environment + Record of collaboration with scientists and other stakeholders at external enterprises + Record of patents and publications + Record of adhering to and promoting lab safety practices **Why Choose Us?** +… more
    Sanofi Group (10/10/25)
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  • Project Manager

    Catalent Pharma Solutions (Chelsea, MA)
    …GEA Niro SD1, SD4 and SD7, the latter being the largest Good Manufacturing Practice ( cGMP ) unit of its kind for DPI in North America. Catalent Pharma Solutions is ... hiring Project Manager. The Project Management function is responsible for managing the non-technical aspects of projects at Catalent Boston which include customer projects for the development and manufacturing of inhalation products and oral spray dried… more
    Catalent Pharma Solutions (10/10/25)
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  • Analytical Principal Scientist (Analytical team…

    Sanofi Group (Cambridge, MA)
    …+ Ability to operate independently and to prioritize + Familiarity with cGMP and regulatory requirements on analytical methods + Prior CMC project management ... experience + Excellent communications skills **Preferred Qualifications** + Ability to propose course of action and to provide strong advocacy in CMC team meetings + Having a record of success in CMC project management + Having working knowledge of synthetic… more
    Sanofi Group (10/10/25)
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  • Manager, Quality Operations - Vaccine

    Sanofi Group (Waltham, MA)
    …quality related decision making. + Help establish and maintain phase-appropriate cGMP compliance for product manufacturing, testing and stability; leading the team ... to ensure appropriate review and approval of master production records (internal/external) executed production records (internal), in-process and release testing, specifications, reference materials, test results, etc. + Serve as Quality Assurance for all… more
    Sanofi Group (10/08/25)
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  • Sample Processing Technican - Training Provided!

    BioLife Plasma Services (West Springfield, MA)
    …must also maintain complete and accurate records, in accordance with cGMP . ACCOUNTABILITIES Provide exceptional customer service to internal and external customers ... (5%) Perform all required duties in the area of Sample Processing (including, but not limited to): (95%) Prepare units for frozen storage. Collect and store samples from plasma units for testing. Perform routine maintenance on the freezer including monitoring… more
    BioLife Plasma Services (10/05/25)
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