• Associate Director , CMC

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …well as other research areas centered around rare diseases and immune disorders. **Summary** CMC Lead is responsible for supporting the overall CMC ... based on the project needs and the respective development stage of the project. The CMC Lead will support the Sr. CMC Lead on complex and/or late-stage… more
    Daiichi Sankyo Inc. (04/02/24)
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  • Associate Director , Tech Management…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …The Technology Management (mAb, Drug Substance, Drug Product, or New Modality) Lead is responsible for the management of technology transfer of the manufacturing ... (mAb, Drug Substance, Drug Product, or New Modality) manufacturing, evaluates CMC risks for appropriate escalation, recommends transition milestones and ensures a… more
    Daiichi Sankyo Inc. (06/11/24)
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  • Associate Director , RACMC

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …around rare diseases and immune disorders. **Summary** The Associate Director , RACMC, is responsible for the regulatory CMC (Chemistry, Manufacturing ... serve as G-RACMC lead or regional submission lead . Provide regulatory guidance and strategy to CMC sub-team and G-RA teams along with other functional teams… more
    Daiichi Sankyo Inc. (06/08/24)
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  • Device Regulatory Lead ( Associate

    Sanofi Group (Bridgewater, NJ)
    **Job title: Device Regulatory Lead ( Associate Director )** + Location: Bridgewater, NJ or Swiftwater, PA or Cambridge, MA **About the job** The Global ... team is part of the Global Regulatory Affairs, Regulatory CMC and Device Department within Global R&D. This critical...get started? **Main responsibilities** + Serve as Device Regulatory Lead on assigned project teams (early phase, late stage… more
    Sanofi Group (06/06/24)
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  • Associate Director , Regulatory…

    Merck (Rahway, NJ)
    **Job Description** **Position Description:** ** Associate Director , Regulatory Affairs Liaison- Vaccines and Infectious Disease** The Regulatory Affairs ... Headquarters Associate Principal Scientist supports products in the Vaccine and...reports. The individual may also assist or take the lead in tracking, authoring, shepherding and/or review of responses… more
    Merck (06/06/24)
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  • Associate Director , System Support,…

    Bristol Myers Squibb (New Brunswick, NJ)
    …or more areas (ie, research, analytical, quality, engineering, manufacturing, regulatory CMC , or IT). + Proven ability to understand complex processes/problems and ... through various formats (eg presentations, written proposals, reports, correspondence, lead meetings, face-to-face dialogue, etc.) + Proficiency in data analytics… more
    Bristol Myers Squibb (06/12/24)
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  • Regulatory Operations Specialists - II…

    ManpowerGroup (Rahway, NJ)
    …and providing CVM/FDA support for labeling and chemistry, manufacturing, and controls ( CMC ) submissions. + The specialist position also works as part of a ... compendium; obtains US Free Sales Certificates. + The specialist may lead /support teams on various regulatory topics; optimize procedures, processes, and… more
    ManpowerGroup (06/12/24)
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  • Sr Mgr, Clinical Drug Supply & Logistics

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    …as staff from quality, clinical compliance, regulatory, formulations, and IOPS ( CMC , external manufacturing, stability). **A typical day might include the ... following:** + Serves as lead drug supply manager of a program and/or individual...and delivery to investigator sites. Works with Clinical Logistics Associate to complete this activity and/or handles any/all aspects… more
    Regeneron Pharmaceuticals (05/14/24)
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