• Associate Director, Logistics…

    Merck (Wilson, NC)
    …Reporting into the Director, Logistics and Distribution Technology the Associate Director, Logistics and Distribution Technology will be responsible and ... subject matter expert technical support for distribution and logistics of human health Drug Substance, Drug Product and Finished Goods globally. The Packaging… more
    Merck (08/14/25)
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  • Sr Quality Associate I / II - QA Release

    Grifols Shared Services North America, Inc (Clayton, NC)
    …110 countries and regions. **Hours:** First Shift **Summary:** The Senior Quality Associate I, Quality Assurance may be assigned duties and responsibilities within ... will depend on the assignment and may include; review of manufacturing or testing records, preparation or review of failure investigations, sampling/testing/data… more
    Grifols Shared Services North America, Inc (08/29/25)
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  • Senior Associate Quality Control Support…

    Amgen (Holly Springs, NC)
    …while transforming your career. Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleX Batch facility ... Batch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry...plan to be a carbon-neutral company by 2027. **Senior Associate Quality Control Support -Stability** **What you will do**… more
    Amgen (08/08/25)
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  • Associate Process Engineer, Sterilization

    West Pharmaceutical Services (Kinston, NC)
    Associate Process Engineer, Sterilization Requisition ID: 68159 Date: Aug 16, 2025 Location: Kinston, North Carolina, US Department: Operations Description: At West, ... experience required + 1-3+ year experience in a similar position within the manufacturing industry + Good knowledge of LEAN and 6 sigma manufacturing more
    West Pharmaceutical Services (06/23/25)
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  • Quality Assistant/ Associate Materials…

    Grifols Shared Services North America, Inc (Clayton, NC)
    …and services in more than 110 countries and regions. Quality Assistant/ Associate Materials Evaluation Coordinator Hours: 7:00a - 3:30p **Position Summary:** The ... Quality Operations (QO) Assistant/ Associate Materials Evaluation Coordinator evaluates critical quality attributes (visual, dimensional, functioncoordinates required… more
    Grifols Shared Services North America, Inc (08/28/25)
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  • Lab Associate , Product Development

    Catalent Pharma Solutions (Morrisville, NC)
    **Lab Associate , Product Development** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose ... time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing , Catalent supports the acceleration of development programs and… more
    Catalent Pharma Solutions (08/16/25)
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  • Associate Director, Clean Validation

    Fujifilm (Holly Springs, NC)
    …of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and ... **Position Overview** The Associate Director, Cleaning Validation is responsible for leading...implements, and oversees comprehensive cleaning validation program for multi-product manufacturing suites including Drug Substance, Drug more
    Fujifilm (08/22/25)
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  • Packaging Associate

    Pactiv Evergreen (Mooresville, NC)
    **Overview** **Do you have experience in a manufacturing or warehouse environment packing, packaging, inspecting and enjoy working in a fast paced environment? We ... join our great team.** **Immediately** **Hiring** **Packers! Entry level, Some Manufacturing experience preferred!** All Packaging Associates work on a rotating… more
    Pactiv Evergreen (08/08/25)
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  • Commercial Development Associate - Advanced…

    Fujifilm (Raleigh, NC)
    …in Advanced Therapies, Cell Therapies or Cell and Gene Therapy drug development and/or contract manufacturing /testing organization or a service/product ... **Position Overview** As the Commercial Development Associate , you will lead the identification of new...you. From our Bioprocess Innovation Center to our cGMP-compliant manufacturing site, we thrive on collaboration, creativity, and purpose.… more
    Fujifilm (08/29/25)
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  • Engineering Validation Associate

    Pfizer (Sanford, NC)
    …Excellent attention to detail and a solid understanding of Food and Drug Administration Regulations/Guidance and Good Manufacturing Practices + Strong ... and preventative actions. + Adhere to all company and Good Manufacturing Practices (cGMP) procedures, safety regulations, and participate in the development… more
    Pfizer (08/29/25)
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