• Regulatory Affairs Associate II

    Teva Pharmaceuticals (Weston, FL)
    …and qualifications** + Bachelor's degree or foreign academic equivalent in Regulatory Affairs , Drug Regulatory Affairs , Pharmaceutical Sciences, or a ... job offered or 2 years in a related occupation including Regulatory Affairs Specialist or related pharmaceutical regulatory experience. **Must have experience… more
    Teva Pharmaceuticals (09/24/24)
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  • Associate Director, Regulatory Affairs

    Bausch Health (Bridgewater, NJ)
    …product advertising and promotion review experience. Broad knowledge of the pharmaceutical industry Regulatory Affairs discipline for prescription drugs. + ... Join a team! We are a global diversified pharmaceutical company enriching lives through our relentless drive...efficiencies and compliance. + Works closely with the Regulatory Affairs labeling group regarding package insert changes to assess… more
    Bausch Health (09/24/24)
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  • Director, GMSA Oncology Alliance Medical…

    Merck (Columbus, OH)
    …PharmD, DNP, DO, or MD + 3-5+ years of relevant experience working in the pharmaceutical industry and/or Medical Affairs + Experience working in oncology or in ... **Job Description** **Job Description:** The GMA Oncology Alliance Medical Affairs Director (Dir., AMA) is accountable for supporting Medical Affairs (MA)… more
    Merck (10/03/24)
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  • Associate Medical Director, Medical Affairs

    Regeneron Pharmaceuticals (Sleepy Hollow, NY)
    …vascular diseases required. Additionally, Minimum of 4-6 years' experience in the pharmaceutical industry and/or medical affairs is preferred. Experience and ... Medical Director to join our team! The Associate Medical Director of Medical Affairs is responsible for supporting the development of medical strategy, planning &… more
    Regeneron Pharmaceuticals (09/28/24)
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  • Staff Regulatory Specialist…

    Stryker (Cary, IL)
    …is available at www.stryker.com We are currently seeking a **Staff Regulatory Affairs ** **Specialist** **,** ( ** Pharmaceutical Products** ) to join our ... teams. **What you will do** As the **Staff Regulatory Affairs Specialist** , you will provide information used to...+ A minimum of 2-3 years in a Regulatory Affairs role required. + RAC certification or Advanced Degree… more
    Stryker (07/17/24)
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  • Vice President, US Medical Affairs

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …Years clinical/research/academic experience, preferred - 10 or More Years of pharmaceutical industry experience in Medical Affairs , strategically utilizing ... Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical… more
    Daiichi Sankyo Inc. (09/04/24)
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  • Director, State Government Affairs

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …- 10 or More Years Combined experience working in government, government affairs , trade association, or pharmaceutical company required - Experience working ... is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address...and immune disorders. **Summary** With the Head of Government Affairs & Public Policy, this position will help lead… more
    Daiichi Sankyo Inc. (08/12/24)
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  • Director, Federal Government Affairs

    Bristol Myers Squibb (Washington, DC)
    …Democrats, on company specific issues as well as issues of importance to the pharmaceutical industry. + Collaborate with Corporate Affairs and US Policy & ... more: careers.bms.com/working-with-us . Position Summary The Director of Federal Government Affairs is accountable for shaping health care policy to benefit patient… more
    Bristol Myers Squibb (09/25/24)
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  • Sr Manager Regulatory Affairs

    System One (Florham Park, NJ)
    …pharmacy, bioscience; advanced degree preferred. + 3+ years of experience in regulatory affairs within the pharmaceutical or biotech industry, with a focus on ... Senior Manager, Regulatory Affairs (BRANDED PRODUCTS) Must be local for Florham...contract (renewable) Overview The Contractor - Senior Manager, Regulatory Affairs - Quality of Life (QOL), plays a pivotal… more
    System One (09/05/24)
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  • Vice President, Quality Compliance

    Integra LifeSciences (Princeton, NJ)
    …Medical Device Regulations (CMDR), the EU Medical Device Regulation, Japanese Pharmaceutical Affairs Law, and other applicable regulatory agencies. **SUPERVISION ... regulations, ISO 13485, CMDR, Medical Device Directive Regulation (93/42EEC), Japanese Pharmaceutical Affairs Law, and other national and international… more
    Integra LifeSciences (09/30/24)
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  • Vice President, Quality Operations - Tissue…

    Integra LifeSciences (Princeton, NJ)
    …Medical Device Regulations (CMDR), the EU Medical Device Regulation, Japanese Pharmaceutical Affairs Law, and other applicable regulatory agencies. **ESSENTIAL ... regulations, ISO 13485, CMDR, Medical Device Directive Regulation (93/42EEC), Japanese Pharmaceutical Affairs Law, and other national and international… more
    Integra LifeSciences (09/30/24)
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  • Director, Service & Repair and Distribution…

    Integra LifeSciences (Cincinnati, OH)
    …Medical Device Regulations (CMDR), the EU Medical Device Regulation, Japanese Pharmaceutical Affairs Law, and other applicable regulatory agencies. Additionally, ... regulations, ISO 13485, CMDR, Medical Device Directive Regulation (93/42EEC), Japanese Pharmaceutical Affairs Law, and other national and international… more
    Integra LifeSciences (09/30/24)
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  • Sr. AD, Medical Affairs Strategy Team…

    Boehringer Ingelheim (Ridgefield, CT)
    …healthcare, or equivalent industry with minimum 3+ years' experience in + Medical Affairs roles in the pharmaceutical industry. + Demonstrated experience with ... high regard for our employees. The Sr. AD Medical Affairs Strategy [TA] serves as the subject matter expert...insights into medical tactical plans for effective launches of pharmaceutical products in the US, integrated evidence generation plans,… more
    Boehringer Ingelheim (08/17/24)
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  • Senior Associate Director, Medical Affairs

    Boehringer Ingelheim (Ridgefield, CT)
    …healthcare or equivalent industry with minimum 3 years' experience in Medical Affairs roles in the pharmaceutical industry + Demonstrated experience with ... **Description** The Sr. AD Medical Affairs Strategy Dermatology serves as the subject matter...insights into medical tactical plans for effective launches of pharmaceutical products in the US integrated evidence generation plans… more
    Boehringer Ingelheim (07/27/24)
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  • Director /SAD, Medical Affairs Strategy…

    Boehringer Ingelheim (Ridgefield, CT)
    …healthcare, or equivalent industry with minimum 3+ years' experience in Medical Affairs roles in the pharmaceutical industry + **(Director Level)** Minimum ... equivalent industry with minimum 5+ years' experience in Medical Affairs roles in the pharmaceutical industry +...experience in Medical Affairs roles in the pharmaceutical industry + Education Requirements: + Bachelor's degree required,… more
    Boehringer Ingelheim (10/02/24)
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  • Director/Senior Associate Director, Medical…

    Boehringer Ingelheim (Ridgefield, CT)
    …healthcare, or equivalent industry with minimum 3+ years' experience in Medical Affairs roles in the pharmaceutical industry + **(Director Level)** Minimum ... equivalent industry with minimum 5+ years' experience in Medical Affairs roles in the pharmaceutical industry +...experience in Medical Affairs roles in the pharmaceutical industry + Education Requirements: + Bachelor's degree required,… more
    Boehringer Ingelheim (08/30/24)
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  • Senior /Global Medical Advisor - CNS (Remote)

    Boehringer Ingelheim (Ridgefield, CT)
    …therapeutic area background with a minimum of ten (10) years in the Pharmaceutical Industry (Medical Affairs and/or Clinical Development roles, roles in ... Global Medical Advisor (SR GMA) designs the global Medical affairs strategy for the compounds and leads global strategic...two to five (2-5) years of experience in the Pharmaceutical Industry (Medical Department). + Successful track record in… more
    Boehringer Ingelheim (10/01/24)
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  • Medical Director/Scientific Director, Medical…

    AbbVie (Florham Park, NJ)
    …fellowship is preferred. + Minimum of 2 years of clinical trial or medical affairs experience in the pharmaceutical industry or academia or equivalent. 3+ years ... medical and scientific strategic and operational input into core medical affairs activities such as: health-care professional and provider interactions; generation… more
    AbbVie (09/26/24)
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  • Medical/Scientific Director, Medical…

    AbbVie (Florham Park, NJ)
    …fellowship is preferred. + Minimum of 2 years of clinical trial or medical affairs experience in the pharmaceutical industry or academia or equivalent. 3+ years ... and scientific strategic and operational input into core medical affairs activities such as: healthcare professional/provider interactions (HCPs, Patients and… more
    AbbVie (09/20/24)
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  • Scientific Director OR Medical Director, Medical…

    AbbVie (Mettawa, IL)
    …Medical Doctorate (MD) or equivalent (DO). + Minimum of 2 years of Medical Affairs experience in the pharmaceutical industry. + Knowledge of clinical trial ... on qualifications listed below. The Scientific Director for Medical Affairs in GI Care for exocrine pancreatic insufficiency (EPI)...reports. + Typically, 10+ years of experience in the pharmaceutical industry or equivalent. + Minimum of 4 years… more
    AbbVie (09/21/24)
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