Medical Device Quality Engineer – ISO & CAPA Expert (6mo)

SRG is seeking an experienced Quality Engineer to join a growing medical device business on an initial 6 month contract. You will help maintain and improve QMS in line with ISO 13485 and regulatory requirements, supporting product development and manufacturing worldwide.

Joining a cross‑functional team, you will drive CAPA investigations, root cause analysis, risk management, and continuous improvement across manufacturing and supply chain to ensure compliant, high‑quality medical technologies.

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