• CNC Machinist

    Astrix Technology (Lino Lakes, MN)
    …at the forefront of advanced machining, we specialize in Design for Manufacturability and Development services for the medical device industry and are hiring ... + Ensure compliance with quality standards in a regulated, precision-driven environment ( medical device preferred) **Experience & Qualifications:** + High school… more
    Astrix Technology (07/24/25)
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  • Principal Engineer

    Abbott (St. Paul, MN)
    …of FDA, IEC 60601, GMP, ISO 13485, and ISO 14971 + Prior medical device experience preferred. Apply Now (https://www.jobs.abbott/us/en) **Learn more about our ... medical electrical systems. You will be a key contributor to the design, development and testing activities for complex medical devices. **Who we want:** +… more
    Abbott (07/08/25)
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  • Quality & Commissioning Manager

    NTT America, Inc. (St. Paul, MN)
    …quality and commissioning activities occur at the appropriate times in the construction process . + Works with GDCA Supply Chain to develop Requests for Proposals ... requirements, industry best practices, IEEE, NFPA, ASHRAE Guideline 0 (The Commissioning Process ), and other appropriate guidelines. + Works with GDCA Supply Chain… more
    NTT America, Inc. (07/16/25)
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  • Service Desk Agent

    Cayuse Holdings (St. Paul, MN)
    …and log all customer interactions for escalated matters + Mobile telephony and device support + Video Conference Unit Troubleshooting + IP Telephony setup and ... Creation of end user accounts and setting permissions + Provide end user device management and support, including desktops, laptops, and PDAs + Navigate using remote… more
    Cayuse Holdings (07/31/25)
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  • Senior Engineer

    Abbott (Plymouth, MN)
    …of FDA, IEC 60601, GMP, ISO 13485, and ISO 14971 + Prior medical device experience preferred. Apply Now (https://www.jobs.abbott/us/en) **Learn more about our ... focus in the disposable catheter. You will be a key contributor to the design, development and testing activities for complex medical devices. **Who we want:** +… more
    Abbott (07/03/25)
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  • Product Manager - Laser Processed Components

    TE Connectivity (Plymouth, MN)
    …our customers. With a commitment to progress and an extensive product range, we enable medical device OEMs, large and small, to transform ideas into reality. As ... and more connected world.** ​ **Job Overview** **At TE Medical , our vision is to be your partner of...execution of the product roadmaps. **Market Sensing & Strategy Development ** + Understand and articulate market and industry trends,… more
    TE Connectivity (07/19/25)
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  • Principal R&D Engineer, Brooklyn Center (North)

    Medtronic (Brooklyn Center, MN)
    …to Have (** **Desired & Preferred Qualifications):** + Experience in medical device manufacturing or manufacturing in highly regulated industry/environment ... solve problems, make progress, and deliver meaningful innovations. The Process Engineer will lead the development of...innovations. The Process Engineer will lead the development of manufacturing processes for new components at the… more
    Medtronic (08/16/25)
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  • Staff Software Engineer

    Southern Glazer's Wine and Spirits (Minneapolis, MN)
    …from a wide-ranging menu of our Top Shelf Benefits, including comprehensive medical and prescription drug coverage, dental and vision plans, tax-saving Flexible ... for issues, review technical design specifications, and ensure quality in development practices. Additionally, the Staff Software Engineer guides other engineers in… more
    Southern Glazer's Wine and Spirits (07/12/25)
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  • Value Stream Manager

    Abbott (Minnetonka, MN)
    …+ Minimum 2 years In a high-volume, multi-product manufacturing environment, preferably in the medical device industry + Ability to learn, train, and follow good ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
    Abbott (06/12/25)
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  • Sr. Manager- Software Design Assurance

    Philips (Plymouth, MN)
    …You have a minimum of 8+ years' experience in FDA regulated, IEC 62304 medical device software environments (SiMD/SaMD), with a focus on Software Design ... stand-alone software projects (SaMD) as well as software-related aspects of complex medical systems (SiMD). Manages the development , oversight and execution of… more
    Philips (07/29/25)
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