Global Senior Regulatory Affairs Lead – Medical Devices

A leading medical device company is seeking a Senior Regulatory Affairs Specialist in Illinois. You will plan and execute complex global regulatory projects, ensuring compliance with FDA regulations and managing product submissions. The ideal candidate will have at least 4 years of experience in regulatory affairs and a degree in a life science field. This role is eligible for bonuses and offers a competitive benefits package. Join a company dedicated to diversity and career growth. #J-18808-Ljbffr