MedTech QA Manager: MDR/ISO 13485 Lead, On-Site Eindhoven

A growing MedTech firm is looking for a hands-on Quality Assurance Manager in Eindhoven. You'll be responsible for managing and maturing the Quality Management System (QMS) and ensuring compliance with ISO 13485, MDR, and FDA requirements. Join an international team where you'll play a pivotal role in shaping the QA function and making a real impact in patient care. Competitive salary based on experience plus benefits like stock appreciation rights, a good pension scheme, and 25 holidays are offered. #J-18808-Ljbffr