Qa Specialist, Medical Devices | Iso 13485 & Mdr

25 ott - Argelato
EssilorLuxottica

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 ***** 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-*****-Ljbffr

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