Regulatory Compliance Specialist
Medline Industries
Medline Industries, LP in Mundelein, IL is seeking an Adverse Event Specialist responsible for product complaint remediation and MDR reporting in compliance with FDA requirements. You will review and triage complaints, determine reportability under 21 CFR 803, and prepare submissions via eMDR, while coordinating with Quality, Regulatory Affairs, and R&D to gather needed information. The role requires a Bachelor’s degree with 1+ year of relevant experience and offers a path within a global #J-18808-Ljbffr
Vacancy posted more than 2 months ago
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