• Senior Manager, US Regulatory

    Coty (Morris Plains, NJ)
    …part of the global ingredient policy development and defense. This position reports to the Director , NA Regulatory Affairs and R&D Material Management and is ... Senior Manager, US Regulatory Affairs and Ingredient Support **SENIOR...retailers. + Provide guidance to Product Development regarding OTC labeling and claims. Including working with the global artwork… more
    Coty (08/11/25)
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  • Associate Director , Global TA…

    Gilead Sciences, Inc. (Parsippany, NJ)
    …for regulatory authorities. You will oversee preparation and maintenance of regulatory submissions, regulatory labeling and packaging for assigned ... ad hoc or special projects that continuously improve or otherwise advance Regulatory Affairs capabilities. **EXAMPLE RESPONSIBILITIES:** + As needed, represents… more
    Gilead Sciences, Inc. (08/02/25)
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  • Director , Regulatory Advertising…

    Sumitomo Pharma (Trenton, NJ)
    Regulatory Advertising & Promotion** . The Director is part of the Global Regulatory Affairs (GRA) team based in the US. He/she will primarily function as ... position of ** Director , ...optimize the commercial success of products for clinical trials, labeling , etc. + Develop and maintain productive working relationships… more
    Sumitomo Pharma (07/08/25)
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  • Medical Director , Project Physician,…

    J&J Family of Companies (Titusville, NJ)
    …assurance, quality monitoring & compliance, clinical supplies unit, TA strategy, regulatory affairs , data management, medical writing, biostatistics, global ... adverse events (pre and post-marketing) for relationship to treatment + Assists Regulatory Affairs in determining requirements for any corrective actions or… more
    J&J Family of Companies (07/22/25)
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  • Executive Director , Head…

    Bristol Myers Squibb (Princeton, NJ)
    …and optimize product benefit-risk profiles. The ED works cross-functionally with clinical, regulatory , medical affairs , quality, and commercial teams to support ... submissions + Cross-Functional Leadership and Stakeholder Engagement + Partner with clinical, regulatory , and medical affairs teams to integrate safety insights… more
    Bristol Myers Squibb (07/08/25)
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  • Director , Patient Reported Outcomes

    J&J Family of Companies (Raritan, NJ)
    …America, Raritan, New Jersey, United States of America **Job Description:** ** Director , Patient Reported Outcomes** **About Innovative Medicine** Our expertise in ... at https://www.jnj.com/innovative-medicine **We are searching for the best talent for** **a Director , Patient Reported Outcomes (PRO) to be located in Raritan, NJ,… more
    J&J Family of Companies (08/22/25)
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  • Senior Director Global Commercial Strategy,…

    J&J Family of Companies (Raritan, NJ)
    …to improve patient outcomes. + Collaborate closely with cross-functional partners (eg regulatory , medical affairs , market access, R&D, etc.) to facilitate ... Johnson & Johnson Innovative Medicine is recruiting for a Senior Director Global Commercial Strategy, Neuropsychiatry Marketing **,** located in Raritan, NJ.… more
    J&J Family of Companies (08/23/25)
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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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  • Dist Sci Clin Dev Res MD

    J&J Family of Companies (Titusville, NJ)
    …assurance, quality monitoring & compliance, clinical supplies unit, TA strategy, regulatory affairs , data management, medical writing, biostatistics, global ... adverse events (pre and post-marketing) for relationship to treatment** **Assists Regulatory Affairs in determining requirements for any corrective actions… more
    J&J Family of Companies (08/20/25)
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  • Program Safety Lead, GPS Medical Science

    Ascendis Pharma (Princeton, NJ)
    …all applicable laws and regulations and as appropriate, local and foreign regulatory reporting requirements and for signal detection, evaluation and risk management. ... from any source are reviewed according to ICH-GCP guidelines, regulatory requirements and company SOPs and procedures. . Liaises...Assists in the preparation and revision of company product labeling as appropriate. . Assists in the preparation and… more
    Ascendis Pharma (07/17/25)
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