• Project Director : Pharmaceutical

    The US Pharmacopeial Convention (USP) (Rockville, MD)
    …Public Health, or related field. + 10+ years of experience in pharmaceutical stability, regulatory compliance, and product lifecycle management. + Proven ... and providing reasonable accommodation to individuals with disabilities. **Brief Project Director Overview** The Project Director will lead the implementation… more
    The US Pharmacopeial Convention (USP) (12/16/25)
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  • Director , Global Pharmaceutical

    Merck (Upper Gwynedd, PA)
    **Job Description** The role of Director , Global Pharmaceutical Communications - New Products is a unique opportunity to join our Company, one of the world's ... for this role will work under the guidance of the Executive Director , Global Pharmaceutical Communications, in a fast-paced and ever-changing environment.… more
    Merck (01/08/26)
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  • Director , R&D DD&T Business Partner…

    Takeda Pharmaceuticals (Boston, MA)
    …we do begins with our commitment to putting patients first. As the Director , Technology Business Partner for Pharmaceutical Sciences R&D Data Digital and ... including Tetrascience, QbDVision, PAS-X, SAP or Databricks + Understanding of regulatory standards in pharmaceutical industry **Behavioral Competencies:** +… more
    Takeda Pharmaceuticals (01/09/26)
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  • Director , Pharmaceutical Sciences…

    Takeda Pharmaceuticals (Boston, MA)
    …**Technical Acumen** **:** + Provides scientific leadership and innovation in pharmaceutical research and development. Builds teams across functions and geographies ... their abilities to lead and advance their individual skills of pharmaceutical product development. Demonstrates humility and approachability in encouraging others to… more
    Takeda Pharmaceuticals (01/14/26)
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  • Senior Director , Design & Delivery,…

    Takeda Pharmaceuticals (Boston, MA)
    …PharmSci will lead the global digital product strategy across Takeda's Pharmaceutical Sciences Digital Data & Technology (DDT) portfolio driving innovation and ... leadership in strategic governance forums, investment planning committees, and external regulatory or industry working groups as needed. + Ensures alignment of… more
    Takeda Pharmaceuticals (01/09/26)
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  • Director , Regulatory Affairs CMC

    Taiho Oncology (Princeton, NJ)
    …Value Proposition: Join our dynamic and expanding mid-size company in the role of Director for Regulatory CMC directly reporting to Executive Director , ... requirements and submission processes. + In depth knowledge of global regulatory requirements for pharmaceutical development and manufacturing. + Strong working… more
    Taiho Oncology (12/09/25)
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  • Director , Regulatory Affairs…

    Stryker (Trenton, NJ)
    …disposition and release in addition to Quality Assurance responsibilities.Viewed as pharmaceutical regulatory expert within business. + Leads communication with ... **Position Summary:** The ** Director , Regulatory Affairs - Pharmaceuticals** provides...in external agency audits/inspections. + Stays abreast of external pharmaceutical regulatory requirements and expectations. **Education &… more
    Stryker (01/13/26)
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  • Associate Director , Regulatory

    Sumitomo Pharma (Honolulu, HI)
    …a dynamic, highly motivated, and experienced individual for the position of **Associate Director , Regulatory Affairs (Oncology).** The Associate Director is ... Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in...the US. He/She will primarily function as a regional regulatory leader (RRL) and/or Global Regulatory Leader… more
    Sumitomo Pharma (01/10/26)
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  • Associate Director , Regulatory

    University of Pennsylvania (Philadelphia, PA)
    …and wellness programs and resources, and much more. Posted Job Title Associate Director , Regulatory Job Profile Title Associate Director , Clinical Research ... Job Description Summary With the oversight of the Director , the Associate Director for Regulatory...oversight groups; as well as for external entities including pharmaceutical companies, contract research organizations (CROs), the FDA, and… more
    University of Pennsylvania (01/07/26)
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  • Manager | Associate Director

    Boehringer Ingelheim (St. Joseph, MO)
    …as governance review, project team meetings, planning activities and FDA communications. Associate Director Act as Regulatory Affairs (RA) core or subteam member ... in relevant discipline) with minimum two (2) years related experience in Regulatory Affairs or equivalent/relevant experience in the pharmaceutical industry OR… more
    Boehringer Ingelheim (10/29/25)
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