The role
Keep a 200-person ISO 13485 site audit-ready while improving yield on a new surgical instrument line.
What you’ll do
- Lead CAPA, non-conformance, and root-cause investigations
- Support supplier audits and incoming inspection
- Write and maintain validation protocols (IQ/OQ/PQ)
- Work with production to reduce scrap on Line 3
What you’ll bring
- Degree in engineering or a related science
- 3+ years in a regulated manufacturing environment
- Working knowledge of ISO 13485 or ISO 9001
- Six Sigma Green Belt desirable
What’s on offer
- Early finish on Fridays
- Fully funded Black Belt training
- 8% pension contribution