Global Post-Market Quality Director: Lead Compliance

A leading medical device company is seeking a Director of Post Market Quality Assurance to ensure compliance and effectiveness in post market processes. Responsibilities include leading global QA teams, enhancing regulatory compliance, and managing quality assurance budgets. Ideal candidates will have over 12 years of experience in a regulated industry and strong leadership abilities. This role emphasizes driving quality culture and maintaining stakeholder engagement across the organization. The position is based in Bloomington, IN, and requires global travel. #J-18808-Ljbffr