• Manufacturing Associate III, Upstream Processing

    Endo International (Horsham, PA)
    …III, Upstream Processing works in a hands-on capacity in the cGMP fermentation and production support areas to manufacture collagenase clostridium histolyticum ... work as needed. This role performs and supports fermentation process scale-up, cGMP manufacture and validation efforts, and assists in the authoring and… more
    Endo International (08/08/25)
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  • Equipment Specialist - Vaccines

    Sanofi Group (Swiftwater, PA)
    …and resolves production issues. + Completes tasks and corresponding documentation as required by cGMP . + Works with Lead Technicians as well as Managers to ensure a ... products. + Has a thorough working knowledge of the cGMP 's and works to help others understand. + Identifies...School or equivalent diploma with 3 years' experience in cGMP or Pharmaceutical or manufacturing industry. + Associates with… more
    Sanofi Group (08/08/25)
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  • Production Technician - Vaccine

    Sanofi Group (Swiftwater, PA)
    …aseptic gowning. + Completes tasks and corresponding documentation as required by cGMP to ensure document completion (BFRs, logbooks, forms, etc). Works to prepare ... Physical dexterity. . + Completes tasks and corresponding documentation as required by cGMP to ensure document completion (BFRs, logbooks, forms, etc). + Works to… more
    Sanofi Group (08/02/25)
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  • QA Specialist

    Sanofi Group (Swiftwater, PA)
    …- eye testing a prerequisite) of all products within functional areas. + Perform cGMP audits within functional areas by conducting a thorough review of processes and ... documentation. Identify and communicate cGMP compliance deficiencies to upper management, recommend appropriate corrective...included in the Change Control, so proper assessments of cGMP areas can be evaluated, and risk mitigated. +… more
    Sanofi Group (08/08/25)
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  • Manufacturing Associate I, Manufacturing Support…

    Endo International (Horsham, PA)
    …I, Manufacturing Support Services works in a hands-on capacity in the cGMP production support areas (buffer preparation, equipment cleaning, etc.) to support ... + Performs daily weigh/dispense, buffer preparation, and other process support operations for cGMP manufacture of CCH BDS. + Works in a hands-on capacity to prepare… more
    Endo International (07/30/25)
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  • Associate Director - Supply Chain

    Lilly (Philadelphia, PA)
    …and clinical radiopharmaceutical drug products across a worldwide network of cGMP manufacturing sites. Key focus areas include optimizing the global supply ... and industry standards for pharmaceutical manufacturing + Experience within a CMC/ cGMP role in the radiopharmaceutical industry + Familiarity with collaborative… more
    Lilly (08/08/25)
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  • Production Technician- Vaccines

    Sanofi Group (Swiftwater, PA)
    …patients' quality of life. Our teams follow current Good Manufacturing Practices ( cGMP ) and procedures while working in a fast-paced team environment. **Work ... our injectables in accordance with current good manufacturing practices ( cGMP ) for all relevant regulatory agencies (eg FDA). Positions...+ Completes tasks and corresponding documentation as required by cGMP + Ability to lift between 1 to 50… more
    Sanofi Group (08/08/25)
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  • Production Coordinator - 3rd Shift

    Woodstream (Lititz, PA)
    …and customer policies, safety rules, SOPs, current Good Manufacturing Practices ( cGMP ), and other regulatory requirements (as applicable), including the Union ... management. + Keep all work areas neat, clean, and orderly in compliance with cGMP standards. + Understand the overall workflow for each area of responsibility. +… more
    Woodstream (08/02/25)
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  • Biopharm Manufacturing Associate

    ManpowerGroup (King Of Prussia, PA)
    …and processing issues effectively. **What's Needed?** + BS/BA degree, with cGMP manufacturing experience OR an Associate's degree in Biotechnology or related ... technical field with cGMP manufacturing experience OR High School degree, 1+ years of cGMP manufacturing experience + Strong desire for a background in science… more
    ManpowerGroup (07/31/25)
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  • Director-Analytical Development and QC

    Lilly (Philadelphia, PA)
    …a strong technical background in analytical methods and compliance with CGMP regulations, ensuring the integrity of products from preclinical through ... day-to-day operations of AD/QC labs and AD/QC team and ensure compliance with cGMP regulations, SOPs and HSE procedures. Ensure readiness of AD/QC labs for… more
    Lilly (07/26/25)
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