• Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …as well as other research areas centered around rare diseases and immune disorders. Summary CMC Lead is responsible for supporting the overall CMC strategies ... 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
    HireLifeScience (04/21/24)
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  • 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
    HireLifeScience (04/21/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …in the treatment of multiple myeloma. Legend Biotech is seeking Associate Director , Global Strategy & Investigations Owner/ Lead as part of the Technical ... This individual will be responsible for a global operational strategy and investigations lead / owner for a best-in-class high volume marketed CAR-T product as part… more
    HireLifeScience (04/27/24)
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  • 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 , GMP Quality…

    Sumitomo Pharma (Trenton, NJ)
    …and management of the global contract testing laboratories in partnership with the Company's CMC Team. The Associate Director also participates in drafting ... ** Associate Director , GMP Quality Control** Sumitomo...analyses, reports, and recommend product expiry extensions/reductions, as applicable. Lead and/or present at the Stability and Specification Review… more
    Sumitomo Pharma (04/19/24)
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  • Senior Associate Director

    Boehringer Ingelheim (North Brunswick, NJ)
    …Ingelheim has a career opportunity developing pharmaceutical products as a Senior Associate Director , Analytical Development. We are looking for an individual ... in development. You will represent the Analytical Development function in the CMC -Technical Development Team whenever needed and pro-actively help the team to… more
    Boehringer Ingelheim (02/09/24)
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  • Regulatory Strategist - Associate

    Sanofi Group (Bridgewater, NJ)
    …Global Regulatory Team (GRT), and strategic partner to the Global Regulatory Lead (GRL), the Regulatory Strategist leverages their regulatory expertise to contribute ... business planning, governance, and committees. May be requested to lead Global Regulatory Team meetings + May represent GRT...strategy in collaboration with non-US - non-EU regions / GRA- CMC / GRA-Devices. Attends HA meetings and collaborates with… more
    Sanofi Group (04/09/24)
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  • Associate Director , Business…

    Mitsubishi Chemical Group (Jersey City, NJ)
    …on real-world evidence, and creating hope for all facing illness. The Associate Director , Business Development will seek out potential business opportunities ... efficiently communicating with excellent facilitation. The incumbent will also lead initial partnership, licensing and/or acquisition negotiations with sufficient… more
    Mitsubishi Chemical Group (03/08/24)
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  • Associate Director , Supplier…

    Bristol Myers Squibb (Summit, NJ)
    …their personal lives. Read more: careers.bms.com/working-with-us . Position Summary: The Associate Director Supplier Relationship Manager (SRM) is accountable ... BMS vision. The SRM acts as a manufacturing site lead and is accountable for the performance of the...alignment of objectives and priorities with GO Teams and CMC teams, representing the virtual matrix team and CMOs… more
    Bristol Myers Squibb (04/05/24)
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  • Senior Manager, Global Regulatory Strategy, US…

    AbbVie (Madison, NJ)
    …with multiple driver indications within a Therapeutic Area and support the Manager, Global Regulatory Lead (GRL), Associate Director , or Director , in the ... timely response to Health Authorities during application review. . Support CMC sections of major, complex regulatory submissions, including Investigation New Drugs… more
    AbbVie (03/26/24)
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