• Katalyst HealthCares and Life Sciences (Minneapolis, MN)
    …or equivalent) or a related field. 5-10 years of experience in Supplier Quality Engineering , preferably in the Medical Device Industry. Language Proficiency. ... objectives and goals, providing guidance and support as needed. Requirements: Bachelor's degree in engineering B. Tech / BE preferred (Eg, Mechanical Engineering more
    Upward (07/03/25)
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  • Actalent (Minneapolis, MN)
    …3-5 years of experience in technical writing or technical communications within the medical device industry. Proficiency in Adobe InDesign and Microsoft Office ... Technical Labeling Specialist $45-50/hr Onsite/Hybrid in Minneapolis metro Full-time Job...systems is a plus. Knowledge of regulatory affairs and medical device labeling. Graphic design and editing… more
    Upward (07/24/25)
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  • Engineering Change Specialist

    Abbott (St. Paul, MN)
    …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... in documentation control or technical writing in a regulated industry ( medical device , pharmaceutical, or biotech preferred). Apply Now… more
    Abbott (07/22/25)
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  • Talent Acquisition Specialist

    Medtronic (Minneapolis, MN)
    …Human Resources, Business Administration, or a related field. + Experience recruiting for engineering roles in the medical device , healthcare, or technology ... Day in the Life** Medtronic is seeking a dynamic and experienced Talent Acquisition Specialist to join our team onsite in Minneapolis. This role is responsible for… more
    Medtronic (07/25/25)
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  • Principal Software and Security Compliance Audit…

    Medtronic (Minneapolis, MN)
    …threat modeling, vulnerability scanning tools, and common attack routes is essential. + Medical device engineering experience. + Strong technical and ... Compliance Audit Specialist focus will be primarily medical device software, product security, and risk...devices . + Experience in Quality/Compliance and/or Audit with medical device requirements (eg, MDSAP, EU MDR,… more
    Medtronic (07/29/25)
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  • Regulatory Affairs Specialist II - Ventures…

    Abbott (St. Paul, MN)
    …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... to various international affiliates. + Maintains pertinent domestic and international medical device regulations to ensure submission requirements world-wide are… more
    Abbott (05/17/25)
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  • Sr. Regulatory Affairs Specialist

    Medtronic (Minneapolis, MN)
    …requirements and quality standards + Experience with Class III medical devices (PMA) + History of successful device submissions + Strong negotiation ... EU Notified Body), and working with cross-functional project teams. + 4+ years medical device industry experience + In depth experience with FDA requirements,… more
    Medtronic (07/29/25)
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  • Principal Regulatory Affairs Specialist

    Medtronic (Minneapolis, MN)
    …profile._ + Bachelor's degree in a technical discipline + Minimum 7 Years of medical device regulatory experience with Bachelor's degree + Or minimum 5 Years ... Life** Our Cardiac Rhythm Management Integrated Operating Unit offers devices and therapies that treat patients with abnormal heart...of medical device regulatory experience with an advanced… more
    Medtronic (07/17/25)
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  • Principal Training and Education Specialist

    Medtronic (Plymouth, MN)
    …experience in a clinical lab setting, clinical training, field sales/support in medical device , healthcare industry or equivalent experience. 3 years PAD ... experience in a clinical lab setting, clinical training, field sales/support in medical device , healthcare industry or equivalent experience. 2 years PAD… more
    Medtronic (07/14/25)
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  • Principal Regulatory Affairs Specialist

    Philips (Plymouth, MN)
    Device /HealthTech product environments. Experience with Software as Medical Device (SaMD) and Ultrasound Imaging Devices highly desired. + You have ... preparation and submission of Technical Documentation, 510(k), De Novo, PMA, and registrations of medical devices globally. + You're able to work in a large,… more
    Philips (07/23/25)
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  • Regulatory Affairs Specialist II…

    Abbott (Plymouth, MN)
    …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... to various international affiliates. + Maintains pertinent domestic and international medical device regulations to ensure submission requirements world-wide are… more
    Abbott (06/28/25)
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  • Senior Product Stewardship Specialist

    Abbott (St. Paul, MN)
    …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... Stewardship + Experience in restricted substance management (eg, REACH, RoHS) + Medical device manufacturing experience preferred + Must possess critical… more
    Abbott (07/09/25)
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  • Sr. Clinical Engineer - EP Mapping…

    Abbott (St. Paul, MN)
    …including Clinical Medicine, Engineering , Marketing and Regulatory Affairs required. Medical device industry experience preferred. Training and experience in ... of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines....or, Design Validation and GLP study experience in the medical device industry. + Demonstrated ability to… more
    Abbott (06/13/25)
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  • Technical Communications Specialist

    Actalent (Minneapolis, MN)
    …3-5 years of experience in technical writing or technical communications within the medical device industry. + Proficiency in Adobe InDesign and Microsoft Office ... Technical Labeling Specialist $45-50/hr Onsite/Hybrid in Minneapolis metro Full-time Job...is a plus. + Knowledge of regulatory affairs and medical device labeling. + Graphic design and… more
    Actalent (07/22/25)
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  • Sr. Regulatory Affairs Specialist - ACM

    Medtronic (Mounds View, MN)
    …individuals with a broad background covering the total regulatory life cycle of medical devices and strong working knowledge and experience with reviewing ... **A Day in the Life** The Senior Regulatory Affairs Specialist (Sr. RAS) is responsible for collaborating, planning and...advertising and promotional materials for medical devices . The initial project scope for… more
    Medtronic (07/01/25)
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  • Medical Science Clinical Research…

    Medtronic (Mounds View, MN)
    …advancing the cardiac rhythm management (CRM) operating unit (OU) via critical medical science initiatives, inclusive of external research. Ideal role for a ... in the intersection of strategic and operational aspects, as this involves reviewing medical science work in a visible position, while maintaining sight of various… more
    Medtronic (07/29/25)
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  • BIM/VDC Specialist I

    Kraus-Anderson (Minneapolis, MN)
    …by the Engelsma family for more than 70 years, KA is consistently ranked by Engineering News Record among the top 50 general contractors in the United States. Our ... is broken; providing cost analyses, scheduling information, and value engineering services to ensure that our client can make...highest quality and the best value. **Summary** The BIM/VDC Specialist I supports the BIM/VDC team by assisting with… more
    Kraus-Anderson (07/28/25)
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  • Product Development Specialist

    3M (Maplewood, MN)
    …, product engineering , product development, and/or research laboratory supporting medical devices or chemistry-based product lines. + Three (3) years ... **Job Description:** Product Development Specialist **Collaborate with Innovative 3Mers Around the World**...+ Bachelor's degree or higher in a science or engineering discipline (completed and verified prior to start) +… more
    3M (07/16/25)
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  • Clinical Specialist

    Abbott (Minneapolis, MN)
    …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... to CRM Sales Representatives. **Required Qualifications** + Bachelor's degree in Bio- Medical Engineering , related field or equivalent healthcare experience. +… more
    Abbott (07/29/25)
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  • Sr. Quality Assurance Specialist

    Philips (Plymouth, MN)
    …Bachelor's OR 3+ years of experience with Master's in areas such as Medical Device , Quality Assurance, Quality Control, Quality Audit, Compliance Coordination or ... **Sr. Quality Assurance Specialist for Service Enablement** **In this role you**.../ Master's Degree in Quality Management, Supply Chain Management, Engineering , Science or equivalent. + 5+ years of experience… more
    Philips (07/26/25)
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