• Insmed Incorporated (San Diego, CA)
    …for each other, and for the future of science, we're in. Are you?About the Role:The Director , Regulatory Affairs will serve as the regulatory leader on ... teamsWith oversight from the VP of Regulatory Affairs , lead the development and implementation of global... Affairs , lead the development and implementation of global regulatory strategy plans to facilitate efficient… more
    HireLifeScience (08/13/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …research areas centered around rare diseases and immune disorders. Summary The Associate Director , Global Oncology Medical Affairs , Medical Analytics will be ... Affairs Impact and Omnichannel strategy. This is a global role which will work across regions, functions and...of related experience working in data analytics in commercial, regulatory , market access or medical affairs function… more
    HireLifeScience (10/12/25)
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  • Formation Bio (New York, NY)
    …bring new treatments to patients faster and more efficiently.About the PositionThe Senior Director , Regulatory Affairs lead is responsible for developing and ... science or healthcare preferred or equivalent relevant experience. Has 10-20 years of Regulatory Affairs experience as well as additional experience in the… more
    HireLifeScience (10/10/25)
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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 ... understanding of US, EU, and Japanese regulations for human drugs/biologics.Knowledge of global regulatory guidance documents and regulations with emphasis on… more
    HireLifeScience (09/08/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …for continuous quality improvement.Deputize for the Sr. Director , Medical Affairs QA as needed. Cross-functional and Global Team Participation:Drive quality ... and immune disorders. Job Summary: Reporting to the Sr. Director , Medical Affairs QA, the Director...or clinical development. requiredMust possess a solid understanding of global health authority regulatory requirements particularly in… more
    HireLifeScience (09/03/25)
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  • Insmed Incorporated (NJ)
    regulatory documents for agency meetings.Provide interpretation of applicable FDA/EMA/ICH/WHO global regulations to ensure CMC compliance within regulatory ... agency interactions and product development meetings.Understanding of scientific principles and regulatory CMC requirements relevant to global drug development… more
    HireLifeScience (08/08/25)
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  • Insmed Incorporated (NJ)
    …and for the future of science, we're in. Are you?About the Role:The Medical Director , Medical Affairs - Dermatology role will be responsible for supporting the ... so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of...vision. This position will report directly to the Executive Director of Medical Affairs . Together with the… more
    HireLifeScience (10/11/25)
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  • BeOne Medicines (San Mateo, CA)
    **General** **Description:** The Director , Regulatory Affairs , Dx/CDx and Medical Devices will be responsible for leading a small team for developing and ... is preferred and remote working possible **Location: Remote** **Reports To:** Executive Director , Global Regulatory Strategy, Dx/CDx and Medical Devices.… more
    DirectEmployers Association (10/11/25)
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  • BeOne Medicines (San Mateo, CA)
    **General Description:** The Director , Regulatory Affairs will be responsible for developing, implementing, and advising on North America (NA) regulatory ... line with business objectives, and in coordination with the global regulatory leader and key internal stakeholders....candidates will have experience working as a lead in Regulatory Affairs with the FDA and prior… more
    DirectEmployers Association (09/06/25)
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  • GRAIL (Menlo Park, CA)
    …with the FDA and/or global health authorities. + Support the US Regulatory Affairs team in preparing submissions such as PMAs, 510(k)s, post-approval ... and review of Standard Operating Procedures and policy guidelines within the regulatory affairs department. + Perform other duties as assigned. **Preferred… more
    DirectEmployers Association (08/16/25)
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