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    Analyst, Product Surveillance - Minneapolis, United States - ICONMA

    ICONMA background
    Description
    ·

    May perform multiple functions within the post market surveillance department.
    ·


    Major responsibilities would include determining classification, review, and disposition of adverse events and medically related complaints for on-market products, including decisions on seriousness, reportability, and potential causality.

    ·

    Complete FDA MDR and other outside competent authority regulatory reports.
    ·


    Four-year degree, preferably in the healthcare or science fields; or 2-year degree and relevant experience supporting complaint handling investigations, medical device reporting, or product analysis.

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