QA Specialist, Medical Devices | ISO 13485
EssilorLuxottica is seeking a QA Specialist to join the Quality & Regulatory Affairs team.
Le informazioni riportate di seguito illustrano i requisiti del ruolo, l'esperienza richiesta ai candidati e le qualifiche associate.
The role focuses on maintaining and continuously improving the Quality Management System to ensure compliance with ISO 13485 and MDR across the product lifecycle. xivgfpx
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.
Le informazioni riportate di seguito illustrano i requisiti del ruolo, l'esperienza richiesta ai candidati e le qualifiche associate.
The role focuses on maintaining and continuously improving the Quality Management System to ensure compliance with ISO 13485 and MDR across the product lifecycle. xivgfpx
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.