• Director, Pharmaceutical Sciences Program…

    Takeda Pharmaceuticals (Boston, MA)
    …technical expertise but across Takeda competencies. + Independently leads development of strategy and plans for multiple, complex programs + Regularly leads and ... influences functional/divisional strategy , operations and innovation + Functional thought leader and...Acumen** **:** + Provides scientific leadership and innovation in pharmaceutical research and development. Builds teams across functions and… more
    Takeda Pharmaceuticals (11/06/24)
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  • Medication and Pharmaceutical Policy…

    American Institutes for Research (Rockville, MD)
    …is seeking a confident, self-motivated, and creative **Medication and Pharmaceutical Policy Analyst** to join ourHealth (https://www.air.org/our-work/health) team to ... quality initiatives. Ideally, the candidate will have experience with pharmaceutical care in a clinical or retail setting. The...beyond legal compliance to its full integration in our strategy , operations, and work environment. At AIR, we define… more
    American Institutes for Research (11/16/24)
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  • Director Pharmaceutical Quality Systems

    Fujifilm (Thousand Oaks, CA)
    …our company, our community, and the world at large. The Director, Pharmaceutical Quality Systemswill lead the Quality Systems, Validation, Compliance and Supplier ... system processes. **External US** **Summary of Position:** The Director, Pharmaceutical Quality Systemswill lead the Quality Systems, Validation, Compliance and… more
    Fujifilm (10/10/24)
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  • Director, US Regulatory Affairs…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …thereby accomplishing corporate goals. **Responsibilities:** + Develop and implement US regulatory strategy for assigned project(s). Strategize and plan for ... is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address...with FDA. This role will create and implement effective regulatory strategies to deliver on efficient and robust development… more
    Daiichi Sankyo Inc. (09/02/24)
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  • Post Doctoral Regulatory Affairs Fellow…

    Boehringer Ingelheim (Ridgefield, CT)
    …& Responsibilities** Regulatory Expertise: The Fellow will develop basic regulatory strategy expertise/knowledge in one or more therapeutic areas. Interact ... and RA sub-team, provide leadership in the development and implementation of US regulatory strategy within a global development context. + Assess US strategic… more
    Boehringer Ingelheim (08/31/24)
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  • Senior Quality Operations Manager…

    Procter & Gamble (Greensboro, NC)
    …to lead a team responsible for end-to-end quality assurance in our pharmaceutical & dietary supplement manufacturing facility in Greensboro, NC. This manufacturing ... and initiative delivery at P&G dietary supplement and OTC pharmaceutical manufacturing site. + Own one product form (liquid,...Ideal Candidate + Has a passion for leading quality strategy and teams in a fast-paced environment + Is… more
    Procter & Gamble (11/07/24)
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  • Senior Manager Regulatory Strategy

    Lundbeck (Deerfield, IL)
    Senior Manager Regulatory Strategy - Remote Opportunity Requisition ID: 5804 Location: Deerfield, IL, US Do you want to join a team where the mission is ... Preferably East Coast or Midwest.** **SUMMARY:** The Senior Manager, Regulatory Strategy (US RA): supports the creation...+ Accredited Bachelor's Degree + 7+ years within the pharmaceutical and/or biotech industry or for a consulting company… more
    Lundbeck (10/18/24)
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  • Senior Director Global Regulatory Affairs…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …+ Lead a multidisciplinary Global Regulatory Team (GRT) to develop global regulatory strategy and plans for assigned global projects. Gain endorsement from ... is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address... risks, and opportunities in the development of global regulatory strategy and plans, considering therapeutic area… more
    Daiichi Sankyo Inc. (10/01/24)
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  • Associate Director, US Regulatory Affairs…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …growth, thereby accomplishing corporate goals. **Responsibilities** + Develop and implement US regulatory strategy for assigned project(s). + Strategize and plan ... is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address...with FDA. This role will create and implement effective regulatory strategies to deliver on efficient and robust development… more
    Daiichi Sankyo Inc. (09/18/24)
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  • Future Opportunities - Join Our Talent Pipeline…

    AbbVie (North Chicago, IL)
    …Affairs Strategy roles (US and Canada) are: 1. Responsible for providing regulatory strategy & support for global development. 2. Responsible for supporting ... Area Head with the development & execution of the regulatory strategy . 7. Serve as HA liaison...R&D, or Industry-related experience is required. 2-3 years in pharmaceutical regulatory activities is preferred. + Demonstrates… more
    AbbVie (09/20/24)
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  • Director, US Regulatory Affairs…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …or More Years in the pharmaceutical industry + 4 or More Years in regulatory affairs, NDA, sNDA, BLA filing to FDA **Travel** Ability to travel up to 30% ... is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address...FDA; direct, coordinate and implement the preparation of all regulatory submissions and provide regulatory support across… more
    Daiichi Sankyo Inc. (11/09/24)
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  • Future Opportunities - Join Our Talent Pipeline…

    AbbVie (Irvine, CA)
    …and considered for future opportunities. The Director Regulatory Affairs Global Regulatory Lead, Global Regulatory Strategy , is responsible for ... regulatory dossiers. + May lead the Labeling Regulatory Strategy Team (LRST), and serve as...management skills. + Preferred Experience: 7-10+ years' experience in pharmaceutical regulatory activities, with experience as lead… more
    AbbVie (09/20/24)
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  • Director, Regulatory Affairs…

    Regeneron Pharmaceuticals (Tarrytown, NY)
    The Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical ... Regulatory filings and provide regulatory leadership on...you bring good understanding of US FDA and international pharmaceutical guidance, regulations, drug development process, and industry standard… more
    Regeneron Pharmaceuticals (11/09/24)
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  • Executive Director, Regulatory

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …team advancing Regeneron's vibrant pipeline in the area of general medicine within the Regulatory Strategy group in Regulatory Affairs. The incumbent will ... to interact with senior managers in the company on regulatory strategies for product development. This management position in...or MD. + A minimum of 15 years of pharmaceutical industry or related experience, at least 5 of… more
    Regeneron Pharmaceuticals (11/20/24)
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  • Global Regulatory Strategy

    AbbVie (North Chicago, IL)
    …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Global Regulatory Strategy Infrastructure Intern Overview Envision spending your ... in one of the most dynamic organizations in the pharmaceutical industry. This is a reality for AbbVie's Experiential...is a reality for AbbVie's Experiential Interns. The Global Regulatory Strategy Infrastructure Intern will support the… more
    AbbVie (10/26/24)
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  • Associate Director, Regulatory Affairs

    Sumitomo Pharma (Columbus, OH)
    Regulatory Leader (RRL) and is responsible for ensuring the execution of regional regulatory strategy in line with the global registration strategy of a ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations...to contribute to the development and writing of a regulatory strategy document in coordination with clinical… more
    Sumitomo Pharma (11/21/24)
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  • Director, Global Regulatory Affairs CMC

    Takeda Pharmaceuticals (Lexington, MA)
    …executes and manages regulatory submissions per the GRA CMC Product Team technical regulatory strategy + Guide the team to define and drive strategy ... in a GRA CMC Product Team lead role, prepares and maintains relevant regulatory documentation (eg, technical regulatory strategy documents, storyboards, risk… more
    Takeda Pharmaceuticals (11/10/24)
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  • Regulatory Affairs Senior Manager…

    Amgen (Washington, DC)
    … activities to ensure effective FDA interactions consistent with the Global Regulatory strategy -includes contingency regulatory planning/risk assessment + ... regulatory documents and meetings in accordance with GRT strategy (eg, responses to regulatory agency questions)...Qualifications:** Doctorate degree and 2 years of experience in regulatory or pharmaceutical drug development Or Master's… more
    Amgen (11/24/24)
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  • Head, Global Regulatory Operations

    Takeda Pharmaceuticals (Boston, MA)
    …Operations at Takeda will be responsible for formulating and implementing the Global Regulatory Affairs Operations (GRA-Ops) vision and strategy to achieve a ... and complexity of technical knowledge) + Comprehensive understanding of the pharmaceutical industry, R&D, and regulatory affairs + Experience managing… more
    Takeda Pharmaceuticals (10/24/24)
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  • Regulatory Affairs Director

    Kelly Services (Ballwin, MO)
    …Benefits (Health/Dental/Vision insurance, performance-based bonus, etc.) **Key Responsibilities:** + ** Regulatory Strategy Development:** Develop and implement ... all regulatory activities, especially CMC aspects of new API and pharmaceutical product development. **Title** : Regulatory Affairs Director **Location** :… more
    Kelly Services (11/23/24)
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