• Novo Nordisk Inc. (Plainsboro, NJ)
    …This individual works cross-functionally with internal and external departments on Regulatory Affairs labeling related issues. Relationships Reports to labeling ... rapport and working relationships with company stakeholders. Effective collaboration with Regulatory Affairs , CMR, Supply Chain, and HQ colleagues regarding… more
    HireLifeScience (11/08/24)
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  • Aequor (Swiftwater, MN)
    …Writes and approves CMC regulatory documents/dossiers to be dispatched to regulatory affairs functions for submissions Coordinates CMC writing performed by ... Overview of the Position The Regulatory CMC Specialist will work closely...Experience Bachelor's degree in Biological Sciences with 2&plus years Regulatory Affairs experience OR Master's degree in… more
    HireLifeScience (11/02/24)
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  • Merck & Co. (North Wales, PA)
    …operates under the guidance of the Associate Director who supports the Global Regulatory Affairs & Clinical Safety (GRACS) and Quality Assurance (QA) ... Job Description Position Description: Senior Specialist , Financial Planning & Analysis Our company's mission...analytical support to our Research & Development Division, Global Regulatory Affairs & Clinical Safety (GRACS), and… more
    HireLifeScience (11/07/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …Operations, Market Shaping, Diabetes and Bio Pharm Marketing, Sales, Medical Affairs , Legal, Compliance and other cross-functional stakeholders to plan and manage ... They will regularly interface with their direct report, the Peer-to-Peer Relations Specialist . This role will regularly collaborate with various parts of the… more
    HireLifeScience (10/17/24)
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  • Sr. Specialist , Regulatory

    MicroVention, Inc. (Aliso Viejo, CA)
    …7. Ability to comprehend technical documents and concepts. **External-Facing Title:** Senior Specialist Regulatory Affairs **Posting Country:** US - United ... **12271BR** **Title:** Sr. Specialist , Regulatory Affairs **Job Description:** Responsible for preparing strategy for worldwide product approval timeline,… more
    MicroVention, Inc. (11/11/24)
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  • Sr Specialist , Regulatory

    Fujifilm (Holly Springs, NC)
    …Springs, North Carolina, United States. **External US** **About This Role** The Sr. Specialist , Regulatory Affairs , provides critical insights on FDA and ... expansion project teams, guiding efforts to maintain manufacturing flexibility with minimal regulatory impact. Sr. Specialist establishes and maintains the site… more
    Fujifilm (11/08/24)
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  • Specialist I, Regulatory

    MicroVention, Inc. (Aliso Viejo, CA)
    **11917BR** **Title:** Specialist I, Regulatory Affairs **Job Description:** This position is responsible for assisting in obtaining regulatory approvals ... and concepts. 7. Proficient computer skills (eg, MS Office). **External-Facing Title:** Specialist , Regulatory Affairs **Posting Country:** US - United… more
    MicroVention, Inc. (11/11/24)
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  • Senior Specialist , Regulatory

    BD (Becton, Dickinson and Company) (San Diego, CA)
    **Job Description Summary** As Sr. Specialist of Regulatory Affairs you will be responsible for supporting MMS Dispensing products consisting of Medical ... with associated Software and Accessories on a global basis from a Regulatory Affairs standpoint. Support will consist of new product development, sustaining, and… more
    BD (Becton, Dickinson and Company) (10/04/24)
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  • Specialist , Regulatory

    Integra LifeSciences (Braintree, MA)
    …us are challenging what's possible and making headway to help improve outcomes. The Regulatory Affairs Specialist is an intermediate level role responsible ... current and upcoming regulations in the US, EU, Canada and globally. The Regulatory Affairs Specialist is responsible for providing regulatory input for… more
    Integra LifeSciences (10/15/24)
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  • Principal Specialist Regulatory

    Cordis (Irvine, CA)
    …open to remote. MedAlliance (Cordis) are seeking a highly skilled and motivated Principal Regulatory Affairs Specialist to join our dynamic team. This role ... possess strong clinical experience and a proven track record in regulatory affairs within the medical device industry. **Responsibilities** + Lead regulatory more
    Cordis (11/12/24)
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