Clinical Product Safety & MDR Specialist
Medline
Medline in Mundelein, IL is seeking a Clinical Product Surveillance Specialist to assess complaints, submit MDRs to the FDA, and support post-market surveillance. The role requires a Bachelor’s degree in medical science or healthcare and 2+ years of risk management experience; hybrid work arrangement and competitive benefits. The candidate will analyze patient safety data, coordinate with QA and product teams, and ensure regulatory compliance across multiple jurisdictions. #J-18808-Ljbffr Medline
Vacancy posted 4 days ago
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