EU MDR Submissions Regulatory Affairs Associate

A medical device company in Portland, Oregon is seeking a Regulatory Affairs Associate to oversee EU MDR submissions. The role involves managing document preparation, ensuring compliance with regulations, and collaborating with various teams for technical documentation. Candidates should have a minimum of two years of experience in regulatory affairs and a strong understanding of EU MDR requirements. This position offers extensive benefits including medical, dental, vision, and 401(k) plans. #J-18808-Ljbffr