• Sr. Regulatory Compliance Specialist

    Hologic (Marlborough, MA)
    …a global impact in the medical device industry? Hologic is seeking a ** Senior Regulatory Compliance Specialist** to lead the charge in ensuring our corporate ... business needs. **Experience** + A minimum of 5 years of experience in Medical Device Regulatory Affairs , with a proven track record in domestic and… more
    Hologic (05/23/25)
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  • Director, Global Regulatory Labeling…

    Takeda Pharmaceuticals (Boston, MA)
    …represented at the Labeling cross functional teams, including clinical, safety, medical affairs , and commercial, to ensure unparalleled communication ... bring life-changing therapies to patients worldwide. Join Takeda as Director, Global Regulatory Labeling Strategy where you will be responsible for the development… more
    Takeda Pharmaceuticals (06/04/25)
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  • Director, RA Global Regulatory Lead

    AbbVie (Waltham, MA)
    …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Director Regulatory Affairs Global Regulatory Lead, Global Regulatory ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...product(s) in the assigned therapeutic area. Leads the Global Regulatory Product Team (GRPT). Continually expands TA knowledge, and… more
    AbbVie (04/04/25)
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  • Senior Medical Director

    Astrix Technology (Boston, MA)
    ** Senior Medical Director** Clinical Boston, MA, MA, US Pay Rate Low: 220000 | Pay Rate High: 250000 + Added - 28/05/2025 Apply for Job We are partnered with a ... cutting edge biotech organization in a search for a Senior Medical Director focused in clinical development, who will lead the clinical development execution for… more
    Astrix Technology (05/29/25)
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  • Senior Clinical Research Director,…

    Sanofi Group (Cambridge, MA)
    …Development Plan (in close cooperation with other members of the team, particularly Regulatory Affairs and Health Economics); adjusts and updates the strategy ... The role of the Senior CRD is to: + Provide ophthalmology focused medical and scientific expertise to the cross functional project team to conduct the clinical… more
    Sanofi Group (04/22/25)
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  • Senior Manager, Clinical Supply Chain

    Sumitomo Pharma (Boston, MA)
    …supplies on multiple clinical programs. In addition, working closely with CMC, Regulatory Affairs , Quality Assurance, Clinical Operations, and /or SMPA external ... highly motivated, and experienced individual for the position of ** Senior Manager, Clinical Supply Chain** . The Senior...local regulations. + Collaborate closely with Clinical Operations, CMC, Regulatory Affairs , QA, and PDM to ensure… more
    Sumitomo Pharma (05/20/25)
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  • Senior Counsel

    Fujifilm (Boston, MA)
    **Position Overview** We are hiring a Senior Counsel to provide strategic legal counsel for FUJIFILM Holdings America Corporation (HLUS) and its ink and chemicals ... Reporting to the Division General Counsel, Electronics, M&A & Assistant Secretary, the Senior Counsel, will be responsible for handling all legal affairs more
    Fujifilm (05/14/25)
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  • Senior Quality Engineer I - Design…

    Integra LifeSciences (Boston, MA)
    …testing activities. The role works closely with Product Development, Project Management, Regulatory , Marketing and Medical Affairs . **ESSENTIAL DUTIES AND ... in close collaboration with Product Development, Project Management, RA, Marketing and Medical Affairs . Support Design Reviews, Technical Reviews, and Gate… more
    Integra LifeSciences (05/09/25)
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  • Senior Director, Clinical Research,…

    Merck (Boston, MA)
    …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior more
    Merck (05/24/25)
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  • Senior Engineer, Design Transfer Specialist

    Amgen (Cambridge, MA)
    …closely with cross-functional teams, including R&D, manufacturing, quality assurance, and regulatory affairs , to ensure alignment and successful design transfer. ... various global manufacturing sites. This role requires a deep understanding of medical device design, manufacturing processes, and regulatory requirements. Key… more
    Amgen (05/09/25)
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