• Supply Chain Specialist

    Aston Carter (Burnsville, MN)
    About the Role: Join a dynamic Operations Team supporting a fast-growing medical device company. As a Buyer/Planner, you'll play a critical role in scaling ... or related field + 5+ years in supply chain, preferably in complex medical device manufacturing + Strong back ground in purchasing, planning, and scheduling +… more
    Aston Carter (09/10/25)
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  • Principal Cyber Information Assurance Analyst…

    Medtronic (Lafayette, CO)
    …+ Maintain up-to-date knowledge of cybersecurity regulations and standards specific to the medical device industry (FDA, HIPAA, IEC 62443, NIST, NIS 2, etc.). ... GRC (Governance, Risk, & Compliance), or external/internal audit, preferably within the medical device or healthcare industry. + Strong understanding of… more
    Medtronic (09/09/25)
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  • Cleanroom Production Operator

    Aerotek (Carlsbad, CA)
    **_NOW HIRING CLEANROOM OPERATORS FOR A MEDICAL DEVICE COMPANY!_** **Location -** Carlsbad, CA **Shift -** 1st, 2nd, and 3rd Shifts Available **Pay Rate -** $18 ... processes. + Understanding of SOPs and GMP guidelines. + Experience with medical device manufacturing. + Open to training. **_If you are interested and… more
    Aerotek (09/09/25)
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  • Lead Sales Trainer (United States)

    Cordis (Miami Lakes, FL)
    …tailored to advanced sales methodologies and for application in the cardiovascular medical device space + Continuously enhance training frameworks to address ... Experiences** + 8+ years of experience in sales learning & development, medical device sales, or relevant clinical background with a bachelor's degree in… more
    Cordis (09/09/25)
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  • Principal Regulatory Affairs Specialist -CRDN

    Medtronic (Santa Rosa, CA)
    …discipline + Minimum of 7 years of direct Regulatory Affairs experience within the medical device or other regulated industry, + Or advanced degree with a ... minimum of 5 years of Regulatory Affairs experience. + Medical device industry experience with Class I/II/III/IV software products. **Nice To Have:** + Direct… more
    Medtronic (09/09/25)
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  • R&D Engineer Co-Op Spring

    J&J Family of Companies (West Chester, PA)
    …independently on one or multiple projects under general direction + Interest in medical device /orthopedic fields + "Hands-on" engineering student with ability to ... + Technical competencies such as experience with Creo, mechanical testing, and medical device documentation. + Knowledge and experience with Microsoft Office… more
    J&J Family of Companies (09/09/25)
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  • Senior Regulatory Affairs Specialist

    Medtronic (Santa Rosa, CA)
    …applicant profile_ + Bachelor's degree in a technical discipline + Minimum 4 years of medical device regulatory experience + Or minimum 2 years of medical ... Degree + In depth experience with FDA requirements, guidance documents, Medical Device Regulation, ISO 14971, ISO 13485, and other global regulatory requirements… more
    Medtronic (09/09/25)
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  • Director Of Operations

    Actalent (Minneapolis, MN)
    …We're looking for a leader who has successfully scaled operations in a medical device environment-someone who understands what it takes to grow from ... poised for global impact. Skills Continuous improvement, Operations management, medical device , Manufacturing engineering, Lean manufacturing, Process… more
    Actalent (09/09/25)
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  • Director of Manufacturing Quality

    DEKA Research & Development (Manchester, NH)
    …to lead our quality organization and drive excellence across all aspects of our medical device manufacturing operations. This is a unique opportunity for a ... + Minimum 10+ years of progressive quality management direct experience in medical device manufacturing, including responsibility for the quality of shipping… more
    DEKA Research & Development (09/07/25)
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  • Document Control Manager

    Fujifilm (Santa Ana, CA)
    …**A minimum of five (5) years of Quality Assurance and or Document Control in a medical device manufacturer or equivalent.** + **A minimum of four (4) years of ... IVDR 2017/746, ISO 14971, Brazilian GMPs, Health Canada MDR, Australian Medical Device regulations and regulatory requirements for product registrations… more
    Fujifilm (09/06/25)
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