QA Specialist – Medical Devices (ISO 13485) | Impact & Growth
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.
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.