On behalf of our client, a leading international MedTech company, we are currently looking for an experienced Manufacturing Quality Engineer for a long-term project in Zurich.
General Information:
- Start date: August 2026
- Expected end date: December 2027
- Contract: temporary contract via Randstad (employment)
- Location: Zurich
- Home office: 1 day/week
- Workload: 100%
Objective:
In this role, you will support the reduction of the current NCMR and SCN workload, including investigation, documentation, coordination, and closure activities in line with applicable QMS and regulatory expectations.
Your profile:
- Bachelor’s or Master’s degree in Electrical, Mechanical, Industrial, Biomedical Engineering or similar
- 5–8+ years of relevant experience in the MedTech industry
- Knowledge of ISO 13485, FDA 21 CFR 820, ISO 14971, IEC 60601-1, MDSAP, GMP and GDP
- EU MDR experience
- Supplier management experience, including occasional supplier visits
- FMEA / risk analysis experience
- Strong cross-functional coordination skills
- English level: B2–C1
- Accurate documentation style and strong analytical problem-solving skills
- Proficient in PowerPoint, Word, Excel and Visio
Nice to Have:
- SAP
- Windchill
- Epiq or equivalent CAPA / SCN / NCMR system
- Power BI
- TMV/IMV, IQ/OQ/PQ
- Minitab or similar statistical tools
Sounds interesting? Apply now! We are looking forward to receiving your applications.
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