Global Safety
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Medline Industries, LP in Northfield, Illinois, is seeking a senior professional to lead medical device vigilance, drug safety, and consumer-product safety activities. You will oversee adverse-event case management, reporting, coding, and global pharmacovigilance, working across functions to ensure compliance and timely submissions. The role requires a scientific degree, 5+ years in device/pharma QA, and experience with FDA postmarket reporting. #J-18808-Ljbffr