• Staff Product Security Engineer

    J&J Family of Companies (Cincinnati, OH)
    …per design control processes and conform to Industry Standards for Medical Device Software (IEC 62304) **Qualifications / Requirements:** **Education:** ... impact health for humanity. Learn more at https://www.jnj.com **Job Function:** R&D Product Development **Job Sub** **Function:** R&D Software/Systems… more
    J&J Family of Companies (11/22/25)
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  • Director, Quality

    Globus Medical, Inc. (Audubon, PA)
    …advantage but not essential + Minimum of 5 years of experience is needed within Medical Device Quality Assurance/ Quality Systems with experience in FDA and CE ... At Globus Medical , we move with a sense of urgency...The Director will collaborate cross-functionally with Manufacturing, Supply Chain, R&D , and Regulatory teams to maintain a culture of… more
    Globus Medical, Inc. (12/10/25)
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  • Quality Assurance Engineer, 2nd Shift

    ZOLL Medical Corporation (Pawtucket, RI)
    …related discipline * 3+ years related experience in a regulated environment, preferably medical device * Proficient at problem solving* Excellent verbal & ... innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and… more
    ZOLL Medical Corporation (12/06/25)
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  • Principal Electrical Engineer

    Actalent (Newton, MA)
    …and establish best practices for electrical engineering development within a regulated medical device environment. Responsibilities + Lead and resolve complex ... Job Title: Principal Electrical EngineerJob Description Join our innovative R&D organization as a Principal Electronics Engineer, where you will play a pivotal role… more
    Actalent (12/13/25)
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  • Lead Design Assurance Engineer

    Hologic (Marlborough, MA)
    …Management), and EU MDR (Regulation 2017/745). + Advanced understanding of medical device standards, including usability, reliability, electrical safety, and ... As a subject matter expert, you will partner with R&D , Regulatory Affairs, and Manufacturing Engineering teams to embed...Assurance, Quality Engineering, or related technical roles within the medical device industry with a Bachelor's degree… more
    Hologic (10/30/25)
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  • Staff Engineer

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …820, ISO 13485) & risk management (ISO 14971). + Working experience in medical device regulations and submission processes. + Excellent communication of ... of possible** BD is one of the largest global medical technology companies in the world. Advancing the world...associate will bring engineering skills. The associate will support/lead R&D activities. These activities include but not limited to… more
    BD (Becton, Dickinson and Company) (10/07/25)
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  • Principal Firmware Engineer, Motor Control,…

    J&J Family of Companies (Danvers, MA)
    …Experience with BLDC Motor Controls, (FOC, DTC, PAM) + 5+ years of Medical Device development experience **Preferred:** + Hands-on prototype work and functional ... code control (Git), issue tracking (Jira), requirements management (JAMA) + Experience with medical device standards including IEC 62304, 60601, ISO 14971, 13485… more
    J&J Family of Companies (12/09/25)
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  • District Service Manager, CRM

    Medtronic (Milwaukee, WI)
    …years of successful healthcare experience (such as in a hospital, clinic or medical device company NICE TO HAVE - DESIRED/PREFERRED QUALIFICATIONS: * Medtronic ... training, healthcare, technical services or related areas in the medical device industry * Training and experience...to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference… more
    Medtronic (12/09/25)
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  • Senior Firmware Engineer, Abiomed

    J&J Family of Companies (Danvers, MA)
    …+ Strong troubleshooting, problem-solving, and documentation skills. + 2+ years of Medical Device development experience **Preferred:** + Hands-on prototype work ... code control (Git), issue tracking (Jira), requirements management (JAMA) + Experience with medical device standards including IEC 62304, 60601, ISO 14971, 13485… more
    J&J Family of Companies (12/09/25)
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  • Senior Specialist, Regulatory Affairs (bilingual…

    BD (Becton, Dickinson and Company) (Irvine, CA)
    …and speak). + Minimum of 5 years of experience in Regulatory Affairs within the medical device industry, specifically for Class II and/or Class III electronic or ... and Skills required:** + Strong understanding of China, Hong Kong and Taiwan medical device regulations. + Demonstrated experience in preparing and submitting… more
    BD (Becton, Dickinson and Company) (12/03/25)
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