• Endo International (Horsham, PA)
    …helping everyone we serve live their best life. **Job Description Summary** The Associate Director , Manufacturing Operations will provide leadership and ... manufacturing including Upstream Processing, Downstream Processing, and Manufacturing Support. The Associate Director is a member of the site leadership… more
    DirectEmployers Association (10/21/25)
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  • Insmed Incorporated (NJ)
    …other, and for the future of science, we're in. Are you?About the Role:The Associate Director , Regulatory Affairs, CMC will be responsible for reviewing the CMC ... CMC content requirements based on internal technical documents provided by Technical Operations or from CMOs to support development program and life cycle… more
    HireLifeScience (09/08/25)
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  • Associate Director - Automation…

    Lilly (Lebanon, IN)
    …process control engineers and consultants that support the daily operations of the Biologics facility. The Associate Director is also responsible for the ... make life better for people around the world. The Associate Director -Automation Engineering is responsible for the...necessary systems and business processes required to support GMP operations , and build the site culture. This will require… more
    Lilly (09/27/25)
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  • Associate Director , Materials…

    Lilly (Lebanon, IN)
    …for clinical trial medicines, while also reducing costs and environmental impact. The Associate Director of Materials will lead the planning and procurement of ... direct materials supporting clinical supply manufacturing across small molecule, biologics , and peptides at the Lilly Medicine Foundry. This role ensures on-time… more
    Lilly (09/12/25)
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  • Associate Director Production…

    Charles River Laboratories (Rockville, MD)
    …Compliance is designed into, and maintained, across all strategic initiatives, Operations , functional support organizations, and execution of GMP activities at the ... inspections. This position is responsible for overseeing all quality operations functions, including execution of environmental monitoring, sterility assurance,… more
    Charles River Laboratories (09/11/25)
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  • Associate Director , Strategic…

    Alloy Therapeutics (Waltham, MA)
    …Alloy and our affiliated venture studio, 82VS. The Role The Associate Director , Strategic Initiatives and Business Operations is a versatile and strategic ... capabilities that are foundational for discovering and developing therapeutic biologics . The company facilitates affordable, non-exclusive access to the entire… more
    Alloy Therapeutics (09/23/25)
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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 ... biologics manufacturing facility in compliance with regulatory requirements, including...mitigate risks associated with the therapeutic product lifecycle. The Associate Director collaborates with cross-functional teams to… more
    Fujifilm (08/22/25)
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  • Associate Director , MSAT,…

    Otsuka America Pharmaceutical Inc. (Frankfort, KY)
    **Job Summary** **​** The Associate Director , MSAT - Downstream provides specialized technical leadership and oversight for all downstream manufacturing ... processes for the company's biologics portfolio executed at CDMOs. This role is responsible for ensuring the robustness, scalability, and compliance of downstream … more
    Otsuka America Pharmaceutical Inc. (10/17/25)
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  • cGMP Associate Director , Process…

    University of Southern California (Los Angeles, CA)
    cGMP Associate Director , Process DevelopmentApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/cGMP- ... cell and gene therapies and other biological products for internal/external users. The Associate Director of Process Development (cGMP) is responsible for all… more
    University of Southern California (09/08/25)
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  • Associate Director , CMC Dossier…

    AbbVie (North Chicago, IL)
    …Waltham, MA Leads global regulatory dossier preparation activities for novel biologics by coordinating cross-functional teams of subject matter experts, from ... submission documentation for all phases of clinical development of biologics , with emphasis on later phase programs and marketing...various groups outside of DPD such as Process R&D Operations S&T, preclinical safety, PK, and QA. + Interface… more
    AbbVie (09/13/25)
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