Regulatory & Adverse Event Specialist

A medical device company in Mundelein, IL is looking for an Adverse Event Specialist. This role involves product complaint remediation and processing new complaints for regulatory reportability, ensuring compliance with FDA requirements. Candidates should have a Bachelor's degree, a year of relevant experience, and strong analytical skills. Familiarity with complaint management systems like SAP or TrackWise is beneficial. The position offers a pay rate of $28-31/hour for a 6-month contract. #J-18808-Ljbffr