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 ***** 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.
📌 Qa Specialist, Medical Devices | Iso 13485 & Mdr (Argelato)
🏢 EssilorLuxottica
📍 Argelato
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