• Account Executive, ES (Western PA/Western VA…

    Fujifilm (St. Paul, MN)
    …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... achieving a 10% annual increase of market share. **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're on a mission to innovate for a healthier… more
    Fujifilm (08/15/25)
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  • ENDOSCOPY Clinical Specialist, ESD (Des…

    Fujifilm (St. Paul, MN)
    …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... resource for the Company and its sales team. **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're on a mission to innovate for a healthier world,… more
    Fujifilm (08/09/25)
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  • Account Executive, Surgery Ultrasound - New…

    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 existing customers in their assigned territory. **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're on a mission to innovate for a healthier… more
    Fujifilm (08/01/25)
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  • Specialist, Clinical Apps - MRI

    Fujifilm (St. Paul, MN)
    …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... operation of Fujifilm Magnetic Resonance Imaging Products. **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're on a mission to innovate for a… more
    Fujifilm (07/02/25)
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  • On-Site Centralized Non-Retail Pharmacist (FT)…

    Walgreens (Roseville, MN)
    …analyzing results; and implementing changes. Helps ensure area Pharmacies adhere to regulatory compliance, standard operating procedures and FDA regulations. + ... a remote position.** **Job Summary** Responsible for the implementation of healthcare strategies and driving patient health outcomes. Executes patient intervention… more
    Walgreens (06/06/25)
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  • Technician, Installation (Mechanical)

    Fujifilm (St. Paul, MN)
    …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... new/existing super-conductive MRI systems at customer sites. **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're on a mission to innovate for a… more
    Fujifilm (06/01/25)
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  • Engineer Sr., Manufacturing

    Abbott (Plymouth, MN)
    … requirements. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, operating procedures, ... Abbott is a global healthcare leader that helps people live more fully...Our portfolio of life-changing technologies spans the spectrum of healthcare , with leading businesses and products in diagnostics, medical… more
    Abbott (07/08/25)
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  • Regional Field Director, RNS Program Management

    United Therapeutics (St. Paul, MN)
    …their daughter's pulmonary arterial hypertension (PAH). Today, we have six FDA -approved therapies that treat PAH, pulmonary hypertension associated with interstitial ... products, pumps and disease states, ensuring that physicians, nurses and other healthcare professionals are well versed on PAH disease state, disease progression,… more
    United Therapeutics (08/10/25)
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  • Associate Medical Director, Pharmacovigilance…

    Sumitomo Pharma (St. Paul, MN)
    …and manages Safety Charters + Handles Health Hazard Evaluations and Ad-Hoc Regulatory safety inquiries. + Represents PVRM on post-marketing product specific and/or ... and risk management regulations and guidelines, including pre- and post-marketing US FDA and/or EU ICH safety requirements** + Expertise in medical review of… more
    Sumitomo Pharma (08/15/25)
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  • Manager, Biostatistics

    Sumitomo Pharma (St. Paul, MN)
    …(ISE) strategy for NDA/BLA submissions, ensuring compliance with regulatory expectations. + Collaborate closely with cross-functional teams-including clinical ... writing-to maintain the statistical integrity of study conduct. + Support regulatory submissions by preparing responses to agency inquiries and contributing to… more
    Sumitomo Pharma (08/02/25)
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