Global Adverse Event & Field Action Manager

A global medical device company in Lakewood, Colorado seeks an experienced Manager for Quality in Adverse Event Reporting and Field Action. You will lead initiatives to identify and report adverse events, coordinate cross-functional teams, and oversee regulatory compliance. Candidates should have at least 7 years of experience in medical device vigilance, strong technical writing skills, and the ability to interact with regulatory authorities. The role offers competitive compensation and benefits, with potential for hybrid work arrangements. #J-18808-Ljbffr