• Quality Specialist of Document Management

    embecta (Parsippany, NJ)
    …to enhance efficiency and compliance. + Collaborate with Quality, Manufacturing, Marketing, Medical Affairs , R&D, and Regulatory Affairs teams to ensure ... position is responsible for overseeing document control systems, maintaining regulatory compliance, and driving process improvements across embecta's global… more
    embecta (10/15/25)
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  • Senior Director, Compound Development Team Leader,…

    J&J Family of Companies (Titusville, NJ)
    …via matrix interactions includes individuals from TA strategy, GCSO, global regulatory affairs , project management, finance, legal, quality assurance, quality ... Leadership, Medicines and Device Development and Regulation, Program Management, Regulatory Affairs Management, Relationship Building, Safety-Oriented, Scientific… more
    J&J Family of Companies (11/05/25)
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  • Global Medical Affairs Director - Oncology

    Sanofi Group (Morristown, NJ)
    …scientific exchange and engagement. We serve as key strategic partners for commercial, regulatory , R&D, market access and external affairs to develop and launch ... **Job Title:** Global Medical Affairs Director - Oncology **Location:** Cambridge, MA /...+ Broad drug development experience with robust knowledge of regulatory , market access and reimbursement. + Demonstrated experience in… more
    Sanofi Group (10/02/25)
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  • Director, Materials and Biophysical…

    Merck (Rahway, NJ)
    …with cross-functional teams, including research, development, quality control, and regulatory affairs , to ensure comprehensive biophysical characterization of ... Biology, Process Analytical Technology (PAT), Professional Networking, Quality Control Management, Regulatory Affairs Compliance, Regulatory Compliance, … more
    Merck (11/26/25)
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  • Senior Principal Scientist, Clinical Research,…

    Merck (Rahway, NJ)
    …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... Neuropathic Pain, Neuroscience, Neuroscience Research, Pain Management, Pharmaceutical Development, Regulatory Affairs Compliance, Regulatory Compliance,… more
    Merck (11/19/25)
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  • Clinical Lead, Early Clinical and Experimental…

    Sanofi Group (Morristown, NJ)
    …Clinical Operations (EDCO, including Clinical Trial Managers and Data Managers), Regulatory Affairs , Patients Safety & Pharmacovigilance, Therapeutic Area ... Clinical Operations (EDCO, including Clinical Trial Managers and Data Managers), Regulatory Affairs , Patients Safety & Pharmacovigilance, Therapeutic Area… more
    Sanofi Group (10/07/25)
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  • Assoc Director, Medical Affairs

    Gilead Sciences, Inc. (Parsippany, NJ)
    …experience inOncologyMedicalAffairs + Industry experience with knowledge of all applicable regulatory and legal requirements for Medical Affairs activities + ... visit Gilead.com. We have an exciting opportunity within the US Medical Affairs (USMA) organization for an Associate Director within Oncology Medical Strategy.… more
    Gilead Sciences, Inc. (11/15/25)
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  • Director, NERC Compliance

    NRG Energy, Inc. (Princeton, NJ)
    …or internal NRG data, create reports for internal distribution and collaborate with the Regulatory Affairs and Government Affairs teams to help formulate ... and X. **Job Summary:** As a member of the Regulatory Compliance NERC Team, the Director NERC Compliance provides...experience. + Proven ability to stay current with evolving regulatory changes, NERC O&P standards, and guidelines. + Demonstrated… more
    NRG Energy, Inc. (11/11/25)
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  • Associate Director, Global Regulator Strategy,…

    Bristol Myers Squibb (Madison, NJ)
    …(Masters, PhD, PharmD, BSN, etc.) with at least 3+ years of Regulatory Affairs experience in the pharmaceutical industry. **Key Competency Requirements** ... personal lives. Read more: careers.bms.com/working-with-us . **Associate Director, Global Regulatory Strategy, Neuroscience** **Position Summary:** The selected candidate will… more
    Bristol Myers Squibb (11/26/25)
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  • Senior Director, Global Clinical Development…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …including INDs, IBs, clinical study reports, and NDAs/BLAs. + Collaborate with regulatory affairs on interactions with global health authorities. + Provides ... to post commercialization, with emphasis on the large global clinical trials and regulatory filing activities. The Senior Director, GCD is responsible for all the… more
    Otsuka America Pharmaceutical Inc. (11/18/25)
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