Offer summary
Qualifications:
Degree in Computer Science or Medical Engineering, Knowledge of regulatory requirements for medical devices, Experience in software development projects in medtech, Familiarity with software quality standards, Experience in risk management for MDR.Key responsabilities:
- Support quality management for software and firmware
- Analyze market feedback and assist in post-market surveillance
- Coordinate communication among development, risk management and regulatory affairs
- Conduct software product verification and assist in design transfer
- Support validation of computer systems for software applications
