Regulated QA Engineer – Medical Devices (ISO13485/GMP)

Corin Group is seeking a proactive QA Quality Engineer to bolster the Quality Assurance function. You will ensure products and processes meet ISO13485 and GMP standards while supporting cross‑functional teams in investigations, documentation and continuous improvement.

You will review SOPs and specs, assist with audits, and help manage CAPA/NCR activities. A GMP environment background and strong analytical skills are essential.

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