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

25 ott - Funo
EssilorLuxottica

pEssilorLuxottica 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. /ppThe role involves cross-functional collaboration with Production, RD, Regulatory Affairs and suppliers, handling CAPAs, non-conformities, audits, and quality records to drive compliance and excellence. /p #J-18808-Ljbffr

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