Title: Adverse Event Specialist Location: Mundelein, IL Work Type: Hybrid (Tue-Thurs onsite) Duration: 3 to 6 months Pay: $28-$30/hr Must Have: 5+ years of experience in complaint handling, adverse event reporting, MDR evaluation, post-market surveillance, or regulatory affairs within the medical device or pharmaceutical industry. Strong working knowledge of FDA Medical Device Reporting regulations (21 CFR 803) and complaint handling requirements (21 CFR 820.198) Experience preparing and submi