• Global Regulatory Affairs

    Sanofi Group (Morristown, NJ)
    **Job Title:** Global Regulatory Affairs CMC lead **Location:** Framingham, MA, Morristown, NJ **About the Job** Are you ready to shape the future of ... through strategic negotiations with health authorities worldwide. Within Sanofi's Global Regulatory Affairs (GRA) CMC organization, the CMC Lead role… more
    Sanofi Group (10/15/25)
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  • Global Regulatory Affairs

    Sanofi Group (Morristown, NJ)
    **Job title** : Global Regulatory Affairs Device Lead...of products. The team is part of the GRA CMC & GRA Device Department within Global R&D. ... Your skills could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team supporting… more
    Sanofi Group (10/23/25)
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  • Regulatory Strategist

    Sanofi Group (Morristown, NJ)
    …you'll drive breakthroughs that could turn the impossible into possible for millions. Our Global Regulatory Team is involved in developing regulatory product ... of drug products. As a key member of the Global Regulatory Team (GRT), and strategic partner...industry experience, including at least 3 years of relevant Regulatory Affairs experience or Advanced degree (PharmD,… more
    Sanofi Group (11/07/25)
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  • Global Project Head, Rare

    Sanofi Group (Morristown, NJ)
    …with all key stakeholder in GPT and Global Brand Team (GBT) + Defines global project plans and regulatory strategy together with the GPT members; leads the ... R&D components of the brand optimization strategy in close collaboration with Market Access, Global Commercial and Medical Affairs , as Active member of GPT. +… more
    Sanofi Group (10/29/25)
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  • Assoc Prin Scientist, Regulatory Liaison

    Merck (Rahway, NJ)
    **Job Description** Associate Principal Scientist Regulatory Affairs - Oncology At our company, we aspire to be the premier research-intensive biopharmaceutical ... and attending Agency meetings as needed to assist the global regulatory lead. + Participating as an...colleagues in Regulatory Operations, Clinical Safety, Labeling, Regulatory CMC , and other functional areas. +… more
    Merck (11/11/25)
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  • Regulatory Strategist

    Sanofi Group (Morristown, NJ)
    …of relevant pharmaceutical/biotechnology experience, including at least 4 years of relevant Regulatory Affairs experience (regional and global ), in early ... teams accelerate progress. As a key member of the Global Regulatory Team (GRT), and strategic partner...and late stage, development of multiple modalities; experience within regulatory CMC not directly applicable. + Demonstrated… more
    Sanofi Group (09/24/25)
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  • Executive Director, Global Program Lead…

    Bristol Myers Squibb (Princeton, NJ)
    …and in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** Global Program Leads within the ICV Global Program Leadership ... late-stage challenges (eg, trends in disease area therapeutic advances, and evolving regulatory , patient advocacy and market access environments) to create a vision… more
    Bristol Myers Squibb (10/18/25)
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  • GRA Device Lead (Associate Director)

    Sanofi Group (Morristown, NJ)
    …their families. Your skills could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse ... of products. The team is part of the GRA CMC & GRA Device Department within Global ...team creates and maintains strong collaborative working relationships with Global Regulatory Affairs (GRA), Regional… more
    Sanofi Group (09/23/25)
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  • GRA Device Associate

    Sanofi Group (Morristown, NJ)
    …their families. Your skills could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse ... of products. The team is part of the GRA CMC & GRA Device Department within Global ...team creates and maintains strong collaborative working relationships with Global Regulatory Affairs (GRA), Regional… more
    Sanofi Group (09/20/25)
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  • Associate Director, Submission Program Management…

    J&J Family of Companies (Raritan, NJ)
    …operational submission strategy. The SPML will be a key partner to the Global Regulatory Leader (GRL), Compound Development Team Leader (CDTL) and Project ... submission "North Star" based on target label and overall global regulatory strategy. + Driving development of...degree is required, preferably in Life Sciences, Business Management, Regulatory Affairs or a related field. An… more
    J&J Family of Companies (11/07/25)
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