Medline

Medline in Mundelein, IL is seeking an Adverse Event Specialist to manage product complaint remediation and MDR reporting responsibilities. The role requires applying FDA 21 CFR 803 criteria and coordinating with cross-functional teams to ensure accurate reportability decisions. You will review historical and new complaints, determine regulatory obligations, and submit MDRs via the FDA eMDR portal while collaborating with international contacts as needed. #J-18808-Ljbffr

Medline Industries, LP seeks a qualified QC Supervisor to oversee the Quality Control functions at a designated distribution center. You will manage performance, attendance, and reviews for direct reports and coordinate with Branch Management. Responsibilities include training inspectors on QSR/FDA regulations, ensuring regulatory compliance, and guiding day‑to‑day activities. Ability to lift up to 50 pounds and travel state-to-state may be required. #J-18808-Ljbffr