• Central Services Technician III (Lead Cagewash)

    Charles River Laboratories (Cambridge, MA)
    …as AAALAC International accreditation. + Perform animal husbandry duties to maintain quality and health of research animals, to include: perform daily water bottle ... operational and cost efficiencies through the strategic insourcing of GMP , GLP and non-GLP research services from discovery through...we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science… more
    Charles River Laboratories (07/23/25)
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  • Animal Care Technician I

    Charles River Laboratories (Cambridge, MA)
    …In the Animal Care Technician 1 role, you will use existing SOPs and quality assurance standards to monitor, observe, and record animal health and welfare daily, as ... operational and cost efficiencies through the strategic insourcing of GMP , GLP and non-GLP research services from discovery through...we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science… more
    Charles River Laboratories (06/19/25)
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  • Facilities Manager

    Medtronic (Billerica, MA)
    …Experience in a medical device, biotech, or pharmaceutical setting. + Familiarity with GMP , ISO, or FDA -regulated environments. + Working knowledge of building ... services. + Manage facility-related vendors and service contracts, ensuring high- quality performance and cost-effectiveness. + Collaborate with EHS, quality more
    Medtronic (08/08/25)
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  • Change Analyst

    Kelly Services (Raynham, MA)
    …CO process. + Accountable for compliance with the Food and Drug Administration s FDA Quality System Regulation QSR as it pertains to Documentation and ... information as requested. + Administer the Periodic Review process for controlled Quality documents + Manage Designated Alternate Signature forms + Proactively seek… more
    Kelly Services (08/08/25)
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  • Production Technician

    Globus Medical, Inc. (Methuen, MA)
    …we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team is inspired by the ... is responsible for assembling electro-mechanical medical devices in compliance with applicable FDA , state, OSHA, and ISO regulations and standards, for ensuring that… more
    Globus Medical, Inc. (08/08/25)
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  • Senior Commissioning/Validation Specialist

    Stantec (Burlington, MA)
    …us create buildings that matter to our world. Together, we are enhancing the quality of life globally through design. Join us and design your place with Stantec. ... related to bio-pharmaceutical dosage forms, nutraceutical facilities and other regulated FDA or similar facilities where drug products are manufactured, stored in… more
    Stantec (08/07/25)
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  • Manufacturing Associate II, Cell Therapy

    Bristol Myers Squibb (Devens, MA)
    …records. + Performing tasks in a manner consistent with the safety policies, quality systems, and GMP requirements. + Completing training assignments to ensure ... flexible, and able to work efficiently with safety and quality in mind, with a good understanding of good...**Knowledge and Skills:** + Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing… more
    Bristol Myers Squibb (08/02/25)
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  • Specialist, Lead Manufacturing Associate, Cell…

    Bristol Myers Squibb (Devens, MA)
    …solutions. + Performs tasks in a manner consistent with the safety policies, quality systems, and GMP requirements. Completing training assignments to ensure the ... flexible, and able to work efficiently with safety and quality in mind. We are searching for enthusiastic, and...**Knowledge and Skills:** + Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing.… more
    Bristol Myers Squibb (07/29/25)
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  • Senior Validation Specialist- Computer System…

    Regeneron Pharmaceuticals (Cambridge, MA)
    …will be responsible for planning, executing, and documenting validation activities to meet FDA and potentially other global regulatory standards such as 21 CFR Part ... might include:** + Planning and driving all CSV activities required to maintain quality compliance as per existing Policies and Procedures for RCM. + Generating,… more
    Regeneron Pharmaceuticals (07/26/25)
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  • Manager Trainee - Operations (Travel Program;…

    BioLife Plasma Services (Boston, MA)
    …tasks require prolonged glove wear **PREFERRED QUALIFICATIONS:** + Experience working with SOPs, GDP, GMP , CLIA, and the FDA + Experience working in a highly ... your skills by contributing to financial, marketing, administrative, regulatory, quality , people, and facilities management. + **Contribute to Creating Life-Changing… more
    BioLife Plasma Services (07/22/25)
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