• Associate Director - CMC

    Lilly (Philadelphia, PA)
    …to make life better for people around the world. **Position Overview:** The Associate Director - CMC Regulatory is responsible for leading global CMC ... diagnostic radiopharmaceutical products. This includes the delivery of all relevant CMC regulatory submissions in addition to assessing country-specific … more
    Lilly (08/24/24)
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  • Associate Director , Analytical…

    Gilead Sciences, Inc. (Foster City, CA)
    …aspirations. Join Gilead and help create possible, together. **Job Description** The Associate Director , Analytical Regulatory Science, collaborates with ... be accountable for the interpretation and implementation of new and existing CMC regulatory guidelines and regulations to ensure approvability globally.… more
    Gilead Sciences, Inc. (08/28/24)
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  • Director , CMC Industry…

    Regeneron Pharmaceuticals (Troy, NY)
    The Director of CMC Industry and Regulatory Intelligence is responsible for enabling chemistry manufacturing and controls ( CMC ) quality and compliance ... all CMC operations across Regeneron. As a Director of CMC Industry and Regulatory...health, environment or politics or related degree and: + Associate Director : 15+ years of related experience… more
    Regeneron Pharmaceuticals (09/12/24)
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  • Associate Director / Director

    AbbVie (North Chicago, IL)
    …strong negotiating, influencing, and leadership skills. + Manages completion of CMC regulatory submission documentation for multiple projects of moderate ... the primary Drug Product Development (DPD) representative to interface with the CMC Regulatory group. Develop standard processes and lead CMC project teams… more
    AbbVie (09/20/24)
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  • Senior Scientist / Associate

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …with 8-10 years pharmaceutical industry experience with 4+ years direct or related CMC regulatory experience or + PhD. with 6-8 years pharmaceutical industry ... experience and 4+ years direct or related CMC regulatory experience + Successful track record in preparation, management of review and approval of NDA/MAA/BLA… more
    Daiichi Sankyo Inc. (08/22/24)
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  • Associate Director , CMC Lead

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …project development preferred - 1 or More Years Extensive knowledge of global CMC regulatory requirement and preferably NDA or BLA/MAA submission experiences for ... areas centered around rare diseases and immune disorders. **Summary** CMC Lead is responsible for supporting the overall ...CMC Lead is responsible for supporting the overall CMC strategies within projects, and manage project teams. The… more
    Daiichi Sankyo Inc. (07/01/24)
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  • Associate Director , Statistics…

    AbbVie (Florham Park, NJ)
    …@abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Purpose: The Associate Director in CMC Statistics is responsible for providing ... + Participate in the planning/design, conduct, analysis, and interpretation of CMC studies and regulatory submissions. Participate in establishing departmental… more
    AbbVie (09/20/24)
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  • Sr. Scientist, CMC Development

    Frontier Medicines (South San Francisco, CA)
    Join Frontier Medicines on an exciting journey as our newest Senior Manager/ Associate Director in CMC Development, located at either our Boston or South San ... of our team, reporting directly to the Head of CMC , you'll play an integral role in advancing our...thorough understanding of ICH guidelines, GLP/GMP manufacturing, and related regulatory requirements is required + Ability to travel domestically… more
    Frontier Medicines (08/21/24)
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  • Associate Director

    Ascendis Pharma (Palo Alto, CA)
    …offer a dynamic workplace for employees to grow and develop their skills. The Associate Director , Regulatory Affairs will be responsible for developing and ... implementing global regulatory strategies encompassing clinical, non-clinical and CMC ...team (specifically from: Talent Acquisition Partner or Human Resources Director ) is not allowed. If this occurs your ownership… more
    Ascendis Pharma (07/04/24)
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  • Senior Scientist/ Associate Director

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    Associate Director , RACMC Portfolio Products, will be responsible for regulatory CMC (Chemistry, Manufacturing, and Controls) activities of the portfolio ... be responsible for working on cross-functional teams, developing and executing post-approval Regulatory CMC strategies, reviewing CMC information and data,… more
    Daiichi Sankyo Inc. (07/12/24)
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