QA Specialist: Medical Devices, ISO 13485
EssilorLuxottica is seeking a QA Specialist to join the Quality & Regulatory Affairs team. The role focuses on maintaining the Quality Management System and ensuring compliance with medical device requirements throughout the product lifecycle.
You will collaborate with Production, R&D;, Regulatory Affairs, and external suppliers to support audits, non-conformities, CAPAs, and supplier quality activities. Strong English and documentation skills are essential.
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You will collaborate with Production, R&D;, Regulatory Affairs, and external suppliers to support audits, non-conformities, CAPAs, and supplier quality activities. Strong English and documentation skills are essential.
#J-18808-Ljbffr