Hybrid MDR Adverse Event Specialist
Medline
Medline is seeking an Adverse Event Specialist in Mundelein, IL. The role focuses on reviewing and processing product complaints to determine MDR reportability under FDA regulations (21 CFR 803) and ensuring compliant submissions via the FDA eMDR portal. The position requires a Bachelor’s degree in a relevant field and 1+ year of experience in complaint handling or regulatory affairs. It is a hybrid role with salary range $67,000.00 - $101,000.00 annually and bonus eligibility. #J-18808-Ljbffr Medline
Vacancy posted 1 day ago
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