Senior Q&C Specialist
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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.
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.
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