• Prin Product Security Engineer - Neuro

    Medtronic (Minneapolis, MN)
    …the following tasks: + Product Security - Implement security requirements across the medical device development lifecycle by collaborating with teams to uphold ... strong key management and the use of Hardware Security Modules (HSMs) for medical device protection. + Use of advanced methods like LLMs, Deep learning to… more
    Medtronic (08/20/25)
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  • Sr. Advanced Sourcing Manager

    Olympus Corporation of the Americas (Brooklyn Park, MN)
    …(Supply Chain Management, Engineering, Finance or equivalent) + Supply Chain and/or Medical Device quality certifications or training is desired. + Minimum ... Development support, Vendor negotiations, Purchasing and/or Quality functions, preferably in medical device or other regulated industry. + Minimum of 5 years of… more
    Olympus Corporation of the Americas (08/20/25)
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  • Biomedical Electronics Tech

    UnityPoint Health (Rock Island, IL)
    …for recording in the Clinical Engineering CMMS software database any assigned medical device service or maintenance event performed. All recordings are ... accurate and timely in manner to assure integrity of all CMMS archived medical device and staff work performance history. + Adheres to assigned on-call rotations… more
    UnityPoint Health (08/08/25)
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  • Biomedical Electronics Tech

    UnityPoint Health (Waterloo, IA)
    …for recording in the Clinical Engineering CMMS software database any assigned medical device service or maintenance event performed. All recordings are ... accurate and timely in manner to assure integrity of all CMMS archived medical device and staff work performance history. + Adheres to assigned on-call rotations… more
    UnityPoint Health (08/01/25)
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  • Senior Manager, Project Leadership

    Abbott (Alameda, CA)
    …and work experience + Minimum 10 years of related work experience with medical device product development + Has successfully led several high complexity ... Qualifications:** + Experience designing and implementing design control tools within medical device industry. + Require strong technical experience in… more
    Abbott (07/29/25)
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  • Principal Regulatory Affairs Specialist - US New…

    Abbott (Alameda, CA)
    …US Biologics regulations, US Drug regulations or with EU and other international medical device regulations and submissions. + Familiar with relevant regulatory ... of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000...you dream of. + Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO… more
    Abbott (06/28/25)
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  • Regulatory Affairs Manager - Heart Failure…

    Abbott (Pleasanton, CA)
    …and US device regulations and/or experience with EU and other international medical device regulations and submissions. + Ability to work in a highly ... for US, EU (EU MDR), and other international geographies. + Experience with medical device software requirements and software regulations. + Ability to identify… more
    Abbott (09/15/25)
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  • Field Service Engineer

    IQVIA (Orlando, FL)
    _IQVIA has an opportunity with one of the largest medical device manufacturers in the US. We welcome you to apply if interested! You will be asked to create an ... experience by collaborating with healthcare professionals and leading technical initiatives in medical device technology. You will be responsible for leading a… more
    IQVIA (09/13/25)
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  • Supplier Development Quality Engineer Lead

    Abbott (Pleasanton, CA)
    …This position works out of our Pleasanton, CA location in under the Medical Device , Heart Failure Division. As the Supplier Development Quality Engineer ... such as Quality, Compliance, Engineering, within a regulated environment, such as medical device , diagnostics or pharmaceutical industries, to develop the… more
    Abbott (09/13/25)
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  • Quality Engineer

    Actalent (St. Paul, MN)
    …support for medical devices. + Experience with FDA regulations and other medical device quality standards. + Proficiency in quality tools and methodologies ... production. The position requires 2-5 years of experience, ideally from the medical device industry, but other industries will be considered. You will work… more
    Actalent (09/09/25)
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