EU MDR Regulatory Submissions Specialist

A medical device company in Portland, Oregon is seeking a Regulatory Affairs Associate to manage EU MDR submissions. The role involves collaboration with various teams to ensure compliance and timely submissions. Ideal candidates will have at least 2 years of experience in EU Regulatory Affairs and possess a customer-centric attitude. Benefits include medical, dental, vision insurance, a 401(k) with company match, and paid time off. #J-18808-Ljbffr