Quality Engineer - FDA/ISO 13485 Focus CAPA & QA

Gi Group has a client in Athlone seeking a Quality Engineer to join a highly regulated manufacturing environment. The role focuses on maintaining and improving the Quality Management System and collaborating with cross functional teams across Manufacturing, Engineering and Regulatory.

The ideal candidate will have 3-4 years of experience in QA/Quality Engineering in FDA-regulated settings, with strong knowledge of ISO 13485, CAPA, NCRs and risk management.