• Summer Intern - Regulatory Affairs

    Stryker (Bloomington, MN)
    …out Stryker's mission to make healthcare better. **Opportunities Available** ​ ​ As a Regulatory Affairs Intern, you will gain exposure to regulatory and ... legal frameworks, requirements, and processes that guide medical device development and compliance. In this role, you will support activities such as gathering and… more
    Stryker (09/03/25)
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  • Clinical Affairs Manager, Interventional…

    Teleflex (Minneapolis, MN)
    …with Teleflex IPPs. * Coordinate efforts between cross-functional partners, including Medical Affairs , Global Research & Scientific Services, marketing, and R&D. ... clinical exposure in the medical field in the Cardiology environment. * Medical Device industry supporting Clinical and Medical Affairs , strongly preferred. *… more
    Teleflex (09/13/25)
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  • Senior Manager, Clinical Science, Medical…

    Edwards Lifesciences (Minneapolis, MN)
    …Experience with FDA PMA applications. + Strong knowledge of scientific research methodology, device development process, GCP, ICH guidelines and Global (US FDA, ... Edwards Lifesciences is the leading global structural heart innovation company, driven by a...impact:** + As a key member of the Medical Affairs Clinical Science team, the Senior Manager (formal internal… more
    Edwards Lifesciences (10/17/25)
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  • Project Manager, Med Device , R&D PMO,…

    Eliassen Group (St. Paul, MN)
    …risk management, and communication across all stakeholders. * Coordinate with Regulatory Affairs to ensure documentation and submission readiness for ... **Project Manager, Med Device , R&D PMO, Design Changes** **Anywhere** **Type:** Contract...modifications and component exchange programs while navigating a complex, global matrix organization. The project has completed feasibility and… more
    Eliassen Group (10/25/25)
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  • Regulatory Operations Compliance Project…

    Abbott (Maple Grove, MN)
    …out of our Maple Grove, or St. Paul, MN locations. This Compliance Manager, Global Regulatory Operations would be structured under Global Regulatory ... a regulatory submission. **Preferred** **Qualifications** + Familiarity with Regulatory Affairs departmental responsibilities and processes + Familiarity of… more
    Abbott (09/19/25)
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  • Associate Director, Regulatory Intelligence

    Otsuka America Pharmaceutical Inc. (St. Paul, MN)
    …business development programs. + Build professional network with key stakeholders outside of Global Regulatory Affairs to identify regulatory ... Description** + Oversee the capture, review, and dissemination of global regulatory news, public commenting opportunities, new...technical discipline preferred. + Minimum of 5 years of regulatory affairs experience. + Minimum 2-3 years'… more
    Otsuka America Pharmaceutical Inc. (11/13/25)
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  • Principal Clinical Research Scientist

    Abbott (Plymouth, MN)
    …Operations, Risk Management, Reimbursement, Medical Affairs , Quality, and Regulatory Affairs . You will also interact with global regulatory agencies ... Program Management, Reimbursement, Medical Affairs , Risk Management, Quality and Regulatory Affairs , and investigational sites. + Oversee study Steering… more
    Abbott (10/25/25)
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  • Senior Medical Writer, Clinical Evaluation…

    Abbott (Maple Grove, MN)
    …+ Effectively communicates and collaborates with Sales and Marketing, R&D, Regulatory Affairs , Library Services, Product Performance Group (PPG), Quality ... Abbott is a global healthcare leader that helps people live more...mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more… more
    Abbott (11/07/25)
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  • Medical Writer/Clinical Evaluation Reporting (CER)…

    Abbott (St. Paul, MN)
    …related deliverable as assigned. + Effectively communicates and collaborates with Regulatory Affairs , Marketing Library Services, Product Performance Group ... Abbott is a global healthcare leader that helps people live more...mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more… more
    Abbott (11/01/25)
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  • Sr. Software Quality Engineer

    Medtronic (Mounds View, MN)
    …live case learning opportunities. + Collaborate with cross-functional teams, including R&D, regulatory affairs , and clinical teams, to ensure alignment on ... improving patient outcomes, you'll have the opportunity to impact global healthcare as the usage of Affera grows rapidly...a relevant field. + Certification in quality systems or regulatory affairs (eg, Six Sigma, ASQ, or… more
    Medtronic (11/08/25)
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