Interim MedTech QA Specialist — ISO 13485 & MDR

A MedTech consulting firm is seeking an experienced Interim QA Specialist for a 12-month engagement in Haarlem. In this hybrid role, you will enhance the ISO 13485-compliant QMS, integrate quality management across the product lifecycle, and collaborate with R&D and Operations. A relevant academic background and a strong track record in medical device QA are essential, along with familiarity with regulatory standards. The assignment offers a competitive hourly rate and significant influence on product quality and market readiness. #J-18808-Ljbffr