Qa Specialist, Medical Devices | Iso 13485 & Mdr
EssilorLuxottica 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.
You will collaborate with Production, R&D;, Regulatory Affairs, and suppliers to support audits, CAPAs, non-conformities, and documentation control, driving quality improvements in a dynamic environment.
#J-*****-Ljbffr
You will collaborate with Production, R&D;, Regulatory Affairs, and suppliers to support audits, CAPAs, non-conformities, and documentation control, driving quality improvements in a dynamic environment.
#J-*****-Ljbffr