EssilorLuxottica in Italy is seeking a QA Specialist to join the Quality & Regulatory Affairs team and support the upkeep and continuous improvement of the QMS, ensuring compliance with ISO 13485 and MDR requirements across the product lifecycle.
The role involves cross-functional collaboration with Production, R&D;, Regulatory Affairs and suppliers, handling CAPAs, non-conformities, audits, and quality records to drive compliance and excellence.
📌 QA Specialist – Medical Devices (Casette di Funo)
🏢 EssilorLuxottica
📍 Casette di Funo
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