• Principal Manufacturing Chemist

    Cambrex High Point (Longmont, CO)
    …responsible for overseeing and participating in the technical transfer and execution of GMP and non- GMP manufacturing of intermediate and drug substance API. ... DSDM Manager or Director. Responsibilities Key Job Responsibilities: + Draft non- GMP and GMP batch records from process description using template, as needed.… more
    Cambrex High Point (08/08/25)
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  • Senior Coordinator, Materials Management

    WuXi AppTec (San Diego, CA)
    **Overview** Provides support for shipping and receiving activities, R&D and GMP inventory control, and general warehouse operations. Assists with inventory stocking ... starting materials, active pharmaceutical ingredients (APIs), intermediates, reagents, labels, GMP supplies, and packaging materials. + Supports the maintenance of… more
    WuXi AppTec (08/02/25)
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  • Senior Analyst, QC Cell and Molecular Biology

    Allogene (Newark, CA)
    …Flow cytometry, PCR, and other related testing and will support GMP QC laboratory maintenance by managing and/or monitoring facilities, and laboratory ... and reagents. The incumbent will perform all activities in a GMP environment by accurately following procedures, maintaining accurate and contemporaneous… more
    Allogene (07/23/25)
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  • Manufacturing Technician II

    Cambrex High Point (Longmont, CO)
    …by applying today! Job Overview The Manufacturing Technician II will maintain GMP suites for manufacturing activities by properly setting up, breaking down, ... operating, and cleaning production equipment for both GMP and non- GMP drug substance manufacturing operations. The applicant should have relevant experience with… more
    Cambrex High Point (07/23/25)
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  • Senior Process Development Engineer- Packaging…

    Amgen (New Albany, OH)
    …of diverse and advanced engineering and scientific principles in support of commercial GMP Final Drug Product (FDP) operations in the Amgen Ohio facility. The ... leading the **Commissioning, Qualification and Validation** of process and GMP equipment. They will own the site master validation...They will own the site master validation plan for GMP equipment and will be responsible to the maintenance… more
    Amgen (07/20/25)
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  • Housekeeping Associate

    Abbott (Abbott Park, IL)
    …Lake County. Requires adherence to quality and regulatory requirements (as referenced in GMP 's, SOP's, DEA, OSHA, DEP and Abbott standards). You will also perform ... research laboratories, and common support areas. + Required to complete GMP documentation attestation logs, work orders, training documents. + Required to… more
    Abbott (08/02/25)
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  • Specialist, Quality Assurance

    Merck (De Soto, KS)
    …and oversee compliance and quality-related processes in accordance with applicable GMP requirements and our company's Animal Health Quality Systems. The position ... include:** + Knowledge and experience in assessing quality impact and GMP requirements applicable to qualification and validation of highly complex engineering… more
    Merck (07/31/25)
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  • Maintenance technician- Vaccines

    Sanofi Group (Swiftwater, PA)
    …of all site wide equipment in order to maintain a quality Class A environment in GMP and non GMP facilities at the Swiftwater site. This position reports to and ... Maintenance Technician is a member of a maintenance team that supports GMP and/or non GMP areas at the Swiftwater site. The equipment and systems include both… more
    Sanofi Group (07/22/25)
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  • Facilities & Engineering Manager

    Fortive Corporation (Irvine, CA)
    …engineering, automation systems, and process improvements** in a ** GMP -regulated manufacturing environment** . This role ensures **compliance, efficiency, ... **Facilities & Engineering Management** + Oversee the team responsible for ** GMP facility operations, including cleanrooms, HVAC, utilities, and infrastructure** . +… more
    Fortive Corporation (07/22/25)
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  • Supervisor, Manufacturing Fill Finish

    Catalent Pharma Solutions (Harmans, MD)
    …warehousing. The **Supervisor Fill/Finish** is responsible for supporting the overall GMP Fill Finish manufacturing processes, through the application of broad ... finished drug product biologics for Phase I/II & commercial GMP manufacturing. The Supervisor is critical to our patients....quality compliant operations of the manufacturing process. + Facilitates GMP and Safety training of GMP staff,… more
    Catalent Pharma Solutions (07/15/25)
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