• Senior Scientific Director…

    AbbVie (Irvine, CA)
    …required by program needs, in partnership with Discovery, Translational, and CMC colleagues contribute to design and implement translational strategies. May ... strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and emerging issues.… more
    AbbVie (08/08/25)
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  • Associate Director , CAR-T Analytical…

    J&J Family of Companies (Malvern, PA)
    …single submission. **We are searching for the best talent for an Associate Director , CAR-T Analytical Scientific Integrator - Advanced Therapies to be located in ... Malvern, PA or Leiden, Netherlands.** **Purpose:** The Associate Director , CAR-T Analytical Scientific Integrator will provide analytical, technical and strategic… more
    J&J Family of Companies (07/21/25)
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  • Senior Director Antibody-Drug…

    Lilly (Indianapolis, IN)
    …analytical chemists, bioconjugation scientists, biologics development team, engineers, CMC project management, Lilly manufacturing partners, and regulatory ... portfolio of ADCs that require thorough drug-linker process development and regulatory submission strategies, often with compressed timelines. + Collaborate with… more
    Lilly (07/09/25)
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  • Associate Director - Supply Chain

    Lilly (Philadelphia, PA)
    …to make life better for people around the world. **Position Overview:** The Associate Director , Supply Chain will lead and grow a supply chain team responsible for ... of approved suppliers, products, and components + Review technical and regulatory documentation to ensure accuracy, consistency, and currency of all critical… more
    Lilly (08/08/25)
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  • Head, Analytical Controls (Sr. Director )

    Takeda Pharmaceuticals (Lexington, MA)
    …their teams in the field of analytical controls and compliance + Global CMC program oversight of Pharmaceutical Sciences (PS) with management and oversight of all ... Contribute to overall functional direction globally and represent function within CMC /Pharmaceutical Science and across the global Takeda organization. + Implement… more
    Takeda Pharmaceuticals (06/06/25)
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  • Director , Viral Vector Process Design

    Gilead Sciences, Inc. (Santa Monica, CA)
    …development workflows, and ensure viral safety strategies are aligned with global regulatory expectations. The Director will operate strategically in a highly ... collaborative environment, partnering closely with Research, Analytics, CMC , Regulatory , Commercial Manufacturing, Quality, and external partners. In addition,… more
    Gilead Sciences, Inc. (06/08/25)
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  • Sr. Director Process Translation…

    Lilly (Indianapolis, IN)
    …clinical trial medicines, while also reducing costs and environmental impact. The Senior Director , Process Translation and Execution is directly responsible for ... hybrid and biologics operations as well as onsite lab capabilities. The Senior Director Process Translation will be responsible for providing technical,… more
    Lilly (08/04/25)
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  • Associate Director , Technical PDS&T

    AbbVie (North Chicago, IL)
    …Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Purpose The Associate Director , Technical position within the Product, Development, Sciences and ... direction and management of the PDS&T teams. The Associate Director will provide technical expertise for development of new...products and can represent the company in discussions with regulatory agencies. Due to nature of the projects and… more
    AbbVie (08/03/25)
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  • Exec Director , Program Strategy Leader

    Gilead Sciences, Inc. (Foster City, CA)
    …in some aspects of pharmaceutical manufacturing, or supply chain, or quality, or CMC regulatory , or process development, or as part of a cross-functional ... 35 countries worldwide, with headquarters in Foster City, California. **Executive Director , PDM Product Strategy Leader** **KEY RESPONSIBILITIES** Reporting to the… more
    Gilead Sciences, Inc. (07/15/25)
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  • Associate Director , Clinical Research,…

    Takeda Pharmaceuticals (Lexington, MA)
    …in leading cross-functional clinical programs within Medical Affairs, Clinical Research, Regulatory , CMC or other drug development related function. Clinical ... with significant experience within related functions (eg, Medical Affairs, Clinical Operations, Regulatory , CMC , Marketing). + Minimum of 5 years' experience as… more
    Takeda Pharmaceuticals (08/02/25)
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