QA Specialist, Medical Devices | ISO 13485 & MDR

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/8ljrdx

pEssilorLuxottica 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. /ppYou will collaborate with Production, RD, Regulatory Affairs, and suppliers to support audits, CAPAs, non-conformities, and documentation control, driving quality improvements in a dynamic environment. /p #J-18808-Ljbffr

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/8ljrdx