• Senior Director, Operations CIO - Manuf, Quality…

    Medtronic (Minneapolis, MN)
    …adoption and business impact. + Ensure compliance with all regulatory, audit, and FDA requirements in manufacturing and quality. + Drive accountability and ... We are seeking a dynamic and experienced Senior Director, Operations CIO - Manufacturing , Quality & R&D Enablement to lead IT services and solutions for our… more
    Medtronic (08/27/25)
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  • Senior Software Automation Engineer

    Medtronic (Fridley, MN)
    …in FDA -regulated industries such as medical device or pharmaceutical manufacturing . + Hands-on experience with machine vision systems (eg, Cognex VisionPro). + ... Automation Engineer to lead software and controls integration for automated manufacturing systems. This role requires hands-on experience with Allen-Bradley PLCs,… more
    Medtronic (08/23/25)
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  • Operations Supervisor

    Biomat USA, Inc. (Moorhead, MN)
    …all state and federal regulations, US Food and Drug Administration ( FDA )-approved Standard Operating Procedure Manual, Occupational Safety and Health Administration ... (OSHA), Clinical Laboratory Improvement Amendments (CLIA), Current Good Manufacturing Practice (cGMP) and internal company procedures. * Supervise donor selection,… more
    Biomat USA, Inc. (07/23/25)
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  • Senior Scientist, Particle Engineering

    Balchem (Faribault, MN)
    …in Montvale, New Jersey and we have a broad network of sales offices, manufacturing sites, and R&D centers, primarily located in the US and Europe. Founded in ... of the R&D Group based in Faribault, MN supporting manufacturing locations in Faribault and Albert Lea with occasional...the network. The position reports to the Agglomeration PD&A Manager and will participate in a wide variety of… more
    Balchem (07/23/25)
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  • Senior Import Analyst

    Medtronic (Fridley, MN)
    …with regulatory requirements for US and Canada imports (eg, Customs, FDA , Health Canada, and Participating Government Agencies). Collaborates with 3rd party ... or changes of requirements and analyze impacts related to distribution, manufacturing , or research & development shipments + Support team training including… more
    Medtronic (08/23/25)
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  • Regulatory Affairs Specialist -Cardiac Ablation…

    Medtronic (Mounds View, MN)
    …The Specialist also assists with the license maintenance including renewals, design/ manufacturing change notification, QMS audit, and Manufacturing site ... established procedures. Understands when to escalate matters and gain alignment with manager on work directions and regulatory strategies to determines and develop… more
    Medtronic (08/22/25)
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  • Associate Regulatory Affairs Specialist - CRM

    Medtronic (Mounds View, MN)
    …license renewals and change submissions. + Recommends changes for labeling, manufacturing , marketing, and clinical protocol for regulatory compliance. + Monitors and ... clinical trials applications. + Provide regulatory input for design and manufacturing , including review of specifications, protocols and reports, engineering change… more
    Medtronic (08/26/25)
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  • Senior Quality Engineer (Onsite)

    Olympus Corporation of the Americas (Brooklyn Park, MN)
    …+ Minimum of 5 years of experience in Quality Engineering within an FDA regulated medical device manufacturing environment. + Strong working knowledge of ... quality concepts, including cost of quality, data collection, & reporting. + Support Manufacturing Engineering in the creation of DMR, DHR, routes, and bills of… more
    Olympus Corporation of the Americas (08/22/25)
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  • Continuous Improvement Specialist

    Olympus Corporation of the Americas (Brooklyn Park, MN)
    …. **Job Description** The Continuous Improvement Specialist will support the Manager in driving process improvement initiatives across the organization. This role ... and reduce waste. + Support Continuous Improvement Projects: Work alongside the Manager to plan, execute, and monitor continuous improvement projects. Ensure that… more
    Olympus Corporation of the Americas (07/15/25)
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  • MFG Engineering Technician (On-site)

    GN Hearing (Bloomington, MN)
    …project. 0-1 weeks annually. **Other:** **Other Information** **Direct reports:** Manufacturing Engineering Manager **Indirect reports:** N/A **Working ... **Position Overview** The Manufacturing Engineering Technician is responsible for all production...in a regulated environment (ie ISO 9001, ISO 13485, FDA QSR) + Experience with data acquisition/analysis, and demonstrated… more
    GN Hearing (08/16/25)
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