• Associate Director , MSAT,…

    Otsuka America Pharmaceutical Inc. (Raleigh, NC)
    **Job Summary** **​** The Associate Director , MSAT - Downstream provides specialized technical leadership and oversight for all downstream manufacturing ... business days. **Company benefits:** Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death &… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
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  • 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 ... technical support for distribution and logistics of human health Drug Substance , Drug Product and...technical capabilities lead a global, cross-modality technical team. The Associate Director will lead a team of… more
    Merck (08/14/25)
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  • Associate Director , Small Molecule…

    Otsuka America Pharmaceutical Inc. (Raleigh, NC)
    ** Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance ... at CDMOs + Design and lead method validation and implementation activities for drug substance and drug product ensuring compliance with relevant ICH and… more
    Otsuka America Pharmaceutical Inc. (08/27/25)
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  • Associate Director , Clean…

    Fujifilm (Holly Springs, NC)
    **Position Overview** The Associate Director , Cleaning Validation is responsible for leading and executing Cleaning Validation (CV) activities for a large-scale ... and to mitigate risks associated with the therapeutic product lifecycle. The Associate Director collaborates with cross-functional teams to drive continuous… more
    Fujifilm (08/22/25)
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  • Associate Director QA for Materials,…

    Fujifilm (Holly Springs, NC)
    **Position Overview** The Associate Director , QA for Materials, Supply Chain and QC will be responsible for the supervision of the Quality teams supporting ... open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one… more
    Fujifilm (08/20/25)
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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...Associate QC Stability will report directly to the Director of Quality Control. This individual will act as… more
    Amgen (08/08/25)
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  • Supervisor-Analytical Science

    Cambrex High Point (Durham, NC)
    …analytical development and method onboarding workflows for drug substance and drug product. Reporting to the (Manager, Associate Director , or ... a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug more
    Cambrex High Point (06/24/25)
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  • Area Chief of Staff

    Banfield Pet Hospital (Wilmington, NC)
    …function of the Area Chief of Staff is to lead, develop and manage associate veterinarians in their hospitals to ensure Banfield can attract, develop, engage and ... or local law. Responsible for the ownership and management of the controlled substance inventory for relief doctors. + Own doctor engagement and retention by… more
    Banfield Pet Hospital (08/24/25)
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  • Senior Manager Automation Engineering…

    Amgen (Holly Springs, NC)
    …Automation Engineers accountable for administrating and maintaining automation systems for Drug Substance manufacturing at Amgen North Carolina (ANC). ... (F&E) group, the Senior Manager will work with the Director of Engineering at Amgen North Carolina. This role...and deliver the automation and process control strategy within Drug substance manufacturing. + Serve as an… more
    Amgen (07/25/25)
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  • Senior Scientist Regulatory Compliance

    Cambrex High Point (High Point, NC)
    …is a leading global contract development and manufacturing organization (CDMO) that provides drug substance , drug product, and analytical services across the ... CAPA plans, Change Requests, and Deviations in coordination with the Associate Director , Quality Assurance + Author and Revise Quality Documents where… more
    Cambrex High Point (07/17/25)
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