• Manager , CMC Development…

    Sanofi Group (Morristown, NJ)
    …with the M&S Hubs supporting the technical writing function. + Collaborate closely with Global Regulatory Affairs (GRA) CMC to align on dossier strategies. + ... **Job Title:** Manager , CMC Development and Dossiers **Location**...content generation for reports leading to the authoring of CMC dossier content for regulatory submissions and… more
    Sanofi Group (07/25/25)
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  • Senior Manager , Global Regulatory

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …with 5+ years' experience or Master's degree with 2 years' experience in regulatory affairs or related areas (eg, clinical development, project management, ... needed. - Works collaboratively with members of the global regulatory team (GRL, regional leads, CMC -RA, labeling,...the global regulatory team (GRL, regional leads, CMC -RA, labeling, medical writing, regulatory operations, etc.)… more
    Otsuka America Pharmaceutical Inc. (06/19/25)
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  • Associate Director, Regulatory

    Bausch Health (Bridgewater, NJ)
    …and values drive our collective progress and impact. The Associate Director, Regulatory Affairs handles regulatory development and post-approval/ ... assigned pharmaceutical products. + Coordinate/Liaise with BHC country-specific pharmaceutical Regulatory Affairs personnel for international submissions and… more
    Bausch Health (07/01/25)
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  • Sr. Manager , Supply Chain

    Mitsubishi Chemical Group (Jersey City, NJ)
    …by closely working with MTP internal colleagues in various functions (Quality Assurance, Regulatory Affairs , Marketing, Market Access, Medical Affairs , Drug ... effectively with colleagues in Supply Chain, Accounting, Market Access, Quality Assurance, Regulatory Affairs , Finance, etc. of Mitsubishi Tanabe Pharma Group,… more
    Mitsubishi Chemical Group (06/13/25)
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