• Associate Director

    Sumitomo Pharma (Lincoln, NE)
    …currently seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Director , Regulatory Affairs (Oncology).** The ... Associate Director is part of the Global Regulatory Affairs (GRA) team based in the US. He/She will primarily function as a regional regulatory leader… more
    Sumitomo Pharma (10/11/25)
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  • Associate Director Regulatory

    BD (Becton, Dickinson and Company) (San Diego, CA)
    …become your best self. Become a **maker of possible** with us. **The Associate Director of Regulatory Affairs ** will provide regulatory support for ... regulatory strategies for new product submissions, project management for regulatory affairs submissions, handling existing product registrations including… more
    BD (Becton, Dickinson and Company) (11/21/25)
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  • Manager | Associate Director

    Boehringer Ingelheim (St. Joseph, MO)
    …governance review, project team meetings, planning activities and FDA communications. Associate Director Act as Regulatory Affairs (RA) core or subteam ... **Description** Manager The Manager, Regulatory Affairs (RA) Pharma Safety &...as defined. + Supports specific infrastructural projects as assigned. Associate Director + Responsibility for the safety… more
    Boehringer Ingelheim (10/29/25)
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  • Associate Director , Global…

    Takeda Pharmaceuticals (Cambridge, MA)
    …in order to bring life-changing therapies to patients worldwide. The Associate Director , Global Regulatory Affairs Advertising and Promotion (GRA A&P) ... medicine promotion. **How you will contribute:** + As our Associate Director , Global Regulatory Affairs Advertising and Promotion lead you will act as… more
    Takeda Pharmaceuticals (10/29/25)
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  • Associate Director , US Commercial…

    Bristol Myers Squibb (Madison, NJ)
    …and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director Commercial Regulatory Affairs ** **Description** : The role ... of Associate Director of US Commercial Regulatory Affairs requires the ability to apply complex scientific and expert regulatory advice and risk… more
    Bristol Myers Squibb (12/28/25)
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  • Associate Director

    Kemin Industries (Des Moines, IA)
    Overview Kemin Health is hiring an Associate Director of Regulatory /Scientific Affairs and Quality! In this role, you will be responsible for leading the ... business units' regulatory affairs (RA) and quality assurance (QA) teams by proactively identifying and managing regulatory /quality risks and opportunities… more
    Kemin Industries (12/12/25)
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  • Associate Director / Director

    AbbVie (Mettawa, IL)
    …and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director / Director , International Regulatory Affairs Advertising & ... products and practices to adhere to the highest quality and regulatory standards. The Associate Director / Director will design and deliver optimized… more
    AbbVie (11/25/25)
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  • Associate Director , Global…

    Takeda Pharmaceuticals (Boston, MA)
    … strategies in collaboration with their regional counterparts. **Accountabilities:** + The Associate Director will be responsible for complex or highly complex ... area of regulatory strategy such as understanding broad concepts within regulatory affairs and implications across the organization and globally; proactively… more
    Takeda Pharmaceuticals (11/11/25)
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  • Associate Director

    University of Pennsylvania (Philadelphia, PA)
    …Description Summary With the oversight of the Director , the Associate Director for Regulatory Affairs will oversee the portfolio of clinical research ... undertaken within the department/division. The Associate Director for Regulatory Affairs assists the Director in providing direction and strategic… more
    University of Pennsylvania (10/09/25)
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  • Regulatory Affairs Associate

    GRAIL (Albany, NY)
    …products with the FDA and/or global health authorities. + Support the US Regulatory Affairs team in preparing submissions such as PMAs, 510(k)s, post-approval ... and review of Standard Operating Procedures and policy guidelines within the regulatory affairs department. + Perform other duties as assigned. **Required… more
    GRAIL (12/03/25)
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