QA Specialist, Medical Devices | ISO 13485 & MDR

23 ott - Argelato
EssilorLuxottica

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 13485 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-18808-Ljbffr

Responsabile Tesoreria

24 ott - Catania
EYE Sport

Operations Improvement Specialist – RTW/Woven

24 ott - Trieste
Gruppo Florence

Ricevi nuove offerte di lavoro

Crea una Job Alert gratuita per qa specialist, medical devices | iso 13485 & mdr / argelato

RESPONSABILE DI PRODUZIONE

24 ott - Mantova
Andrea Poletti & Associati

Technical Project Manager

24 ott - Monza
Experis Italia