• Piper Companies (Minneapolis, MN)
    Piper Companies is seeking an Associate Director , Regulatory Affairs to join a top biotechnology company in Minneapolis, MN. Responsibilities of the ... Associate Director , Regulatory Affairs : Lead regulatory documentation and submissions for product development, ensuring compliance with industry… more
    Upward (07/17/25)
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  • Abbott (Alameda, CA)
    …to work for diversity, working mothers, female executives, and scientists. The Opportunity This Associate Director Regulatory Affairs - APAC will work ... CA, location in the Diabetes Division. As a manager, the function of an Associate Director Regulatory Affairs , APAC (Asia Pacific) is to combine… more
    Upward (06/29/25)
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  • EPM Scientific (Bridgewater, MA)
    A leading global pharmaceutical company is seeking an Associate Director of Regulatory Affairs to support regulatory development and post-approval ... focused on delivering better health outcomes through innovation, collaboration, and regulatory excellence. The Associate Director main responsibilities… more
    Upward (07/13/25)
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  • Merck & Co. (Upper Gwynedd, PA)
    regulatory issues to GRACS CMC management, as neededDemonstrate an understanding of regulatory affairs and apply this understanding to the benefit of the ... Job DescriptionGRACS CMC - Associate Principal Scientist, CMC, R4 - Pharm Pre-approval...Regulatory Compliance, Microbiology, Molecular Microbiology, Pharmaceutical Process Development, Regulatory Affairs Compliance, Regulatory more
    HireLifeScience (07/19/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …including working with contract manufacturing organizations CMO. This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub ... applications/supplements & variations (eg, NDA, BLA, MAA). This position authors regulatory documents where necessary with supervision. This position conducts … more
    HireLifeScience (05/15/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …centered around rare diseases and immune disorders. Summary: Responsibility for regulatory strategy to support the development of biomarkers, companion diagnostic ... products.Responsibilities: CDx development : Provide critical strategic and tactical regulatory guidance for CDx/IVD development and CDx submission plan for… more
    HireLifeScience (05/29/25)
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  • Eisai, Inc (Nutley, NJ)
    …a difference. If this is your profile, we want to hear from you. The Associate Director (AD), Global Medical Affairs Training and Education is responsible ... & International). Eisai Salary Transparency Language:The base salary range for the Associate Director , Global Medical Affairs Training and Education… more
    HireLifeScience (06/28/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …research areas centered around rare diseases and immune disorders. JOB SUMMARYThe Senior Director , Head Medical affairs Quality Assurance in Global RD/PV QA is ... strategy and quality plan closely aligned with the Global Oncology Medical Affairs (GOMA), Oncology Business Unit (OBU) and Specialty Business Unit (SBU) Medical… more
    HireLifeScience (04/25/25)
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  • Eisai, Inc (Nutley, NJ)
    …make a difference. If this is your profile, we want to hear from you. Associate Director , Medical Education - Oncology, is responsible for the strategic planning ... & ManagementEisai Salary Transparency Language:The base salary range for the Associate Director , Medical Education - Oncology is from :162,600-213,400Under… more
    HireLifeScience (06/28/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionRole SummaryUnder the guidance of a senior leader, an Associate Principal Scientist/ Associate Director , has primary responsibility for ... is expected to work cross-functionally with clinical development, medical affairs , biostatistics, market access, commercial and country affiliates. The incumbent… more
    HireLifeScience (07/23/25)
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