EssilorLuxottica is seeking a QA Specialist to join the Quality & Regulatory Affairs team. The role focuses on maintaining and continuously improving the Quality Management System to ensure compliance with ISO 13485 and MDR across the product lifecycle. You will collaborate with Production, R&D;, Regulatory Affairs, and suppliers to support audits, CAPAs, non-conformities, and documentation control, driving quality improvements in a dynamic environment. #J-18808-Ljbffr
📌 QA Specialist, Medical Devices | ISO 13485 (Emilia-Romagna)
🏢 EssilorLuxottica
📍 Emilia-Romagna
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