Medical Device QC Specialist
Kerr is seeking a Quality Assurance professional in Italy to support regulatory compliance and product quality for medical devices. The role involves reviewing SOPs, performing inspections, and driving CAPA and NCR processes to ensure patient safety.
You will collaborate with Production, R&D;, and Suppliers, using ISO 13485 and MDR 2017/745 knowledge, and communicate findings in English. A 1–3 year background in a regulated QA environment is preferred.
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You will collaborate with Production, R&D;, and Suppliers, using ISO 13485 and MDR 2017/745 knowledge, and communicate findings in English. A 1–3 year background in a regulated QA environment is preferred.
#J-18808-Ljbffr