- +2
- +2
- Switzerland
About
We are seeking an experienced, detail-oriented, and hands-on QA Engineer/Manager to support the development, regulatory compliance, and lifecycle management of Class III medical device catheters. The ideal candidate will have a strong understanding of ISO, EU MDR, international regulatory requirements, and associated guidance documents. This role requires cross-functional collaboration to ensure compliance in product development, verification and validation requirements, risk management, and post-market activities, while also supporting e.g. biocompatibility, usability, and product safety initiatives.
jid5051f28a jit1042a jiy25aNice-to-have skills
- Risk Management
- Usability Testing
Work experience
- QA Test Automation
- QA Manual Test
Languages
- English