• Director , Clinical Operations

    Bausch + Lomb (St. Paul, MN)
    …areas to provide input on study-related documents and issues (DMP, SAP, drug/ device supplies, CSR, etc.). + Provides clinical operations input in the identification, ... global team members, other B&L departments (eg, R&D/Project Management, Clinical/ Medical Affairs, Biometrics, Regulatory Affairs, Quality Assurance, Pharmacovigilance/GPSS and… more
    Bausch + Lomb (06/07/25)
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  • Sr. Marketing Director , Renal Denervation

    Medtronic (Minneapolis, MN)
    …relevant experience, minimum 10 years of managerial experience) + Experience in the pharma &/or medical device industry + Ability to travel up to 35% of the time ... work together to engineer the extraordinary. The **Senior Global Marketing Director , Market Development** for the **Coronary and Renal Denervation (CRDN)** Operating… more
    Medtronic (07/31/25)
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  • R&D Program Director (CTL) - Mounds View,…

    Medtronic (Mounds View, MN)
    …Have:** + Advanced degree in business, engineering, or a related field + Medical Device industry experience- knowledge of new product development, DRM, clinical ... at Medtronic. At CAS, we are developing next generation medical technologies that treat patients with abnormal heart rhythms....innovation. The key job responsibilities of the R&D Program Director (CTL) are as follows: Business Leadership: * Cast… more
    Medtronic (08/08/25)
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  • Director , Regulatory Affairs

    Philips (Plymouth, MN)
    …experience working in Regulatory Affairs and Quality/Quality Operations within the FDA regulated Medical Device industry, including 3+ years of experience and a ... The Director , Regulatory Affairs will lead the Philips RespirTech...Quality teams. + You have extensive experience/knowledge of global medical device regulations, requirements, and standards (ISO… more
    Philips (07/09/25)
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  • Director of Regulatory, Software…

    Philips (Plymouth, MN)
    …You've acquired 10+ years of experience working in Regulatory Affairs within the medical device industry; Experience with software-enabled medical devices, ... ** Director , Regulatory Affairs- Software and Artificial Intelligence (Ultrasound)**...and all key stakeholders including R&D, Product Management, Quality, Medical & Clinical Affairs, and other functions at all… more
    Philips (08/01/25)
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  • Sr Director , Qrcms IT Solutions

    Medtronic (Mounds View, MN)
    …IT delivery or a related role within a large organization. Experience in the medical device or healthcare industry is a plus. **Skills:** + Deep business ... role will be: * Mounds View, Minnesota **CAREERS THAT CHANGE LIVES** Sr. IT Director for Quality, Regulatory, Clinical, & Medical Sciences (QRCMS) IT Solutions… more
    Medtronic (08/08/25)
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  • Director - KOL Management (Strategic…

    Medtronic (MN)
    …and/or Sales Operations) + 6+ years of experience in the pharmaceutical, biotech, medical device , and/or healthcare industries + Minimum 5+ yrs experience in ... on brand goals and objectives + Partner with Clinical Marketing, Medical Affairs to provide commercial perspective on publications, scientific communications, and… more
    Medtronic (08/09/25)
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  • Director , Biostatistics

    Edwards Lifesciences (Minneapolis, MN)
    …assigned studies + Contributing to additional initiatives that shape the future of medical device development **What you'll need (Required):** + Ph.D. or ... patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will… more
    Edwards Lifesciences (08/08/25)
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  • Sr Director Global Distribution & Logistics…

    Medtronic (Minneapolis, MN)
    …Products: Word, Excel, PowerPoint, Outlook + Knowledge/Experience in Healthcare and/or Medical Device Industry + Knowledgeable in Diabetes Management **Travel:** ... insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/ reimbursement , and Simple Steps (global well-being program). The following… more
    Medtronic (07/30/25)
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  • Sales Specialist, Diagnostic Oncology (West Coast)

    Fujifilm (St. Paul, MN)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... with Key Accounts and Opinion Leaders within the Liver/Hepatology Medical Oncology community. Manage specific assigned geographic areas and successfully… more
    Fujifilm (08/03/25)
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