Senior Q&C Specialist - Medical Devices (EMEA)

<p>Johnson & Johnson MedTech is seeking a Senior Quality and Compliance Specialist to support the EMEA EP organization from the European HQ in Diegem, Belgium. You will lead CAPA/NCR activities, act as Field Action Coordinator, and support audit readiness and regulatory requests. </p><p>The role requires 4–5 years in a regulated medical device environment, knowledge of EU MDR, ERP/QMS experience, and strong English skills. Hybrid work: 3 onsite days, 2 remote days; 12-month contract. </p> #J-18808-Ljbffr