- Bristol Myers Squibb (Princeton, NJ)
- …more: careers.bms.com/working-with-us . **Director, US Franchise and Customer Strategy, Cell Therapy Medical Affairs ** **Location: NJ Based** Join us as we ... expand our cutting-edge Cell Therapy Medical organization. We have an opening for a Director,...**Key Responsibilities** + Contribute to the overall strategy and lead the coordination and execution of the thought leader… more
- Teva Pharmaceuticals (Parsippany, NJ)
- Manager, Regulatory Affairs Date: May 30, 2025 Location: Parsippany, United States, New Jersey, 07054 Company: Teva Pharmaceuticals Job Id: 61105 **Who we are** ... a difference with. **How you'll spend your day** The Manager, Regulatory Affairs will: + Prepare, review and approve regulatory submissions (ie ANDAs, amendments,… more
- Bausch Health (Bridgewater, NJ)
- …of products, primarily in gastroenterology, hepatology, neurology, dermatology, medical aesthetic devices, international pharmaceuticals. Our 7,000 employees share ... our collective progress and impact. The Associate Director, Regulatory Affairs handles regulatory development and post-approval/regulatory compliance for assigned… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …Join Gilead and help create possible, together. **Job Description** The Director of Medical Affairs Research (MAR) is responsible for developing, revising, and ... MAR in compliance related issues. **Essential Duties and Job Functions:** + Lead development and revision of all MA Research procedural documents ensuring the… more
- Bausch Health (Bridgewater, NJ)
- …of products, primarily in gastroenterology, hepatology, neurology, dermatology, medical aesthetic devices, international pharmaceuticals. Our 7,000 employees share ... and direction for the graphics process and systems. Key responsibilities: + Lead preparation, review, and update of content for the development and maintenance… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …activities for all assigned projects in alignment with the Global Regulatory Lead . Translates complex pertinent global requirements and provides an assessment of the ... and manages lifecycle regulatory activities in alignment with the Global Regulatory Lead (GRL). - Identifies the need and obtains regulatory intelligence, researches… more
- Veterans Affairs, Veterans Health Administration (East Orange, NJ)
- …for primary care services, but must also provide indirect oversight for all medical , surgical, and ancillary services provided at NJ VAHCS facilities and its 9 ... Primary Care Physician program and be able to perform, lead , and teach all of the services required in...significant and active role in the selection of applicants. Medical significance, interpretation, and correlation of patient testing data.… more
- Bristol Myers Squibb (Princeton, NJ)
- …for Cell Therapy in Lupus is a core member and leader within the WW Medical Matrix Team. This individual will lead development and implementation of the WW ... an emphasis on CD19 CAR-T and the BMS NEX-T platform. This individual will lead scientific engagement with international lupus experts and represent WW Medical … more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... on timelines or resources, may assist another Global Labeling Lead by managing labeling development or approval for either...required + 4 or More Years of direct regulatory affairs experience, including US labeling experience required + Experience… more
- Bristol Myers Squibb (Princeton, NJ)
- …with 5 years in the industry with at least 4+ years of US Medical Device Regulatory Affairs experience **Key Competencies** + Experience in successfully leading ... landscape, assessing regulatory risk, and developing global filing strategies. + Co- lead marketing application submission teams for indications that are at… more
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