• Medical Device Cybersecurity Analyst

    Compass Group, North America (New Lenox, IL)
    …best practices and risk management of inventoried connected medical devices *Assures compliance with all regulatory standards including patient safety ... Intelas **Position Title:** ** Medical Device Cybersecurity Analyst- New Lenox,...to system-integrated outpatient clinics. With more than 1.15 million medical devices managed, we provide the clarity… more
    Compass Group, North America (09/30/25)
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  • Clinical Product Manager - Medical

    Oracle (Carson City, NV)
    …is standing up a specialized clinical product management team focused on medical device -aligned products. This team bridges clinical practice, product strategy, ... patient safety, usability, and compliance across our next-generation EHR and AI-enabled medical device platforms. As a Clinical Product Manager ( Medical more
    Oracle (11/25/25)
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  • Clinical Product Manager - Medical

    Oracle (Helena, MT)
    …is standing up a specialized clinical product management team focused on medical device -aligned products. This team bridges clinical practice, product strategy, ... patient safety, usability, and compliance across our next-generation EHR and AI-enabled medical device platforms. As a Clinical Product Manager ( Medical more
    Oracle (11/25/25)
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  • Staff Device Engineer

    Takeda Pharmaceuticals (Lexington, MA)
    …product. The Staff Device Engineer has extensive experience in medical devices for drug delivery including combination products, solid understanding ... all the technical aspects of life cycle management of commercialized Combination Products, Medical Devices and pre-filled syringe among others. This role works… more
    Takeda Pharmaceuticals (12/05/25)
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  • Senior Principal Scientist - Device

    Merck (West Point, PA)
    Device Design Control, Medical Device Management, Medical Device Regulations, Medical Devices , Medical Devices Design, Medical ... development including regulatory submission and approval processes. Including development drug- device combination product or a medical device component… more
    Merck (11/18/25)
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  • Principal Scientist, Drug/ Device

    Merck (Rahway, NJ)
    …to foster a culture of operational excellence + Ensure processes align with regulatory requirements for medical device and drug combination products ... related to device -drug integration. + Partner with Quality and Regulatory teams to ensure compliance...devices + Knowledge of US and global combination product/ medical device and healthcare regulations, including FDA… more
    Merck (12/05/25)
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  • Principal Design Quality Engineer…

    Kelly Services (Peachtree Corners, GA)
    …or related scientific field. **Experience:** + Minimum 7 years of experience ( medical device industry preferred). **Skills & Capabilities:** + Strong ... role, you will guide design and development teams to ensure adherence to regulatory and quality requirements. You will lead risk management activities, oversee… more
    Kelly Services (11/25/25)
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  • Principal Engineer Aesthetic Medical

    Bausch Health (Bothell, WA)
    …/ participate in Design and Code reviews Demonstrated experience with Medical Device System/SW verification for Windows CE based devices and Embedded Linux ... aspects of component and systems level verification testing of medical devices . This person will develop and...with other departments to ensure projects conform to all regulatory and quality regulations. Stay up-to-date and… more
    Bausch Health (10/28/25)
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  • (Senior) Manager, Combination Products…

    Takeda Pharmaceuticals (Boston, MA)
    …of commercial products and lifecycle management activities. + Work closely with R&D, Quality , Regulatory , Procurement, and external suppliers to ensure seamless ... and device manufacturing. + Active engagement with Product Operations Lead, Quality , Regulatory , and External CMO Operations & Supply groups to maintain… more
    Takeda Pharmaceuticals (11/05/25)
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  • GRA Device Associate

    Sanofi Group (Cambridge, MA)
    …strategic partner within Sanofi's regulatory framework, providing expert guidance on medical device regulatory requirements across the product lifecycle. ... You'll collaborate across R&D, Device , Manufacturing, and Quality teams while preparing high- quality regulatory...teams. + Contribute to and execute innovative and sustainable medical device regulatory strategies covering… more
    Sanofi Group (09/20/25)
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