• Senior Manager-Clinical Development

    Philips (Cambridge, MA)
    …10+ years' combined experience in Medical Device Clinical Research and Medical Device development within FDA regulated OEM product environments. + You have ... Hospital Patient Monitoring (HPM) Clinical Affairs team, the Senior Manager-Clinical Development is responsible for managing the day-to-day operations of Clinical… more
    Philips (11/05/25)
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  • Senior FW Development Engineer

    Oracle (Boston, MA)
    …bring-up, debugging, implementation and testing. Our product environment covers embedded device development (C/C++), systems management tools (Python, bash), and ... improve, and validate our firmware solutions. You'll contribute to design and development at all software stages-from concept to release-and gain exposure to… more
    Oracle (12/04/25)
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  • Sr. Manager, Human Factors and User Experience

    Takeda Pharmaceuticals (Lexington, MA)
    …labeling etc.) + Oversee or generate the HFE deliverables throughout medical device development (Examples: HFE Plan, Task Analysis, Use Specification, ... of applicable guidance, regulations, standards, and industry best practices to medical device and combination product design and development process. + Support… more
    Takeda Pharmaceuticals (11/14/25)
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  • Advanced Surgical Consultant - Daytona

    J&J Family of Companies (Danvers, MA)
    …Customer Centricity, Innovation, Market Expansion, Market Research, Medicines and Device Development and Regulation, Proactive Behavior, Problem Solving, ... Surgical Consultant. **Purpose:** Heart Recovery, a rapidly growing medical device company, is looking for a driven and results...Team" Specialist. We are growing both our focus and device line-up in order to support Cardiac Surgeons and… more
    J&J Family of Companies (11/19/25)
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  • Regulatory Affairs Associate Director, IVD

    GRAIL (Boston, MA)
    …knowledge of US and international regulatory frameworks and processes for medical device development and approvals. + Effective collaborator in dynamic, ... please visit grail.com . The role assists with regulatory strategy and the development of submissions in partnership with key internal and external stakeholders for… more
    GRAIL (12/03/25)
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  • Director of Human Factors

    Olympus Corporation of the Americas (Westborough, MA)
    …requirements, context of use, verification and validation stages of medical device development . + Experience writing human factors engineering protocols ... a mentor and hands-on multi-disciplinary technical leader with a strong medical device background and excellent communication skills. This position leads the US… more
    Olympus Corporation of the Americas (11/15/25)
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  • Senior Engineer: Mathematical Modeling…

    Amgen (Cambridge, MA)
    …automate model creation and post/processing. + Experience with combination products and device regulatory requirements, medical device development and design ... Product Operations Digital and Data Strategies group is a process development team that develops and deploys innovative advanced simulation technologies towards… more
    Amgen (12/13/25)
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  • Group Engineering Manager - Navigation Hardware

    Globus Medical, Inc. (Methuen, MA)
    …architecture, integration, and lifecycle management. + Proven track record in medical device development or other regulated industries. + Experience with ... engineering principles, ensuring robust hardware solutions and compliance with medical device standards while driving innovation in product development .… more
    Globus Medical, Inc. (12/03/25)
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  • Cdmo-CTO Management Strategy and Operations…

    Takeda Pharmaceuticals (Lexington, MA)
    …Innovation needs working closely with each PharmSci R&D function (Drug Product & Device Development , Analytical Development , Biologics Process Development ... model awareness and consistency + Work closely with PharmSci Leads, Analytical development , Device Development Leads, , and other internal business partners… more
    Takeda Pharmaceuticals (11/26/25)
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  • Medical Device Regulatory Affairs…

    Oracle (Boston, MA)
    …with SaMD in areas such as Regulatory Affairs, Quality Compliance, Product Development , etc. in medical device industry or equivalent. Experience authoring ... the healthcare and life sciences sector. As a Medical Device Regulatory Affairs Strategist, you will work in collaboration...you will work in collaboration with product engineering and development teams and subject matter experts on the total… more
    Oracle (11/25/25)
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