Responsibilities
- Analyze and investigate product complaints from the field
- Open and follow up on life-cycle issues
- Review design specification documents for accuracy, completeness and compliance
- Create test protocols and test reports following execution
- Be involved in the technical design reviews
- Report to the Design QA team leader
Requirements
- B.Sc in Bio Medical Engineering or other relevant degree
- Practical experience of 5-10 years of design quality assurance in medical devices
- Proven skills to perform tasks accurately
- Read, understand and interpret documents such as design specifications, safety rules and technical procedure manuals
- English proficiency at a very high level
- Strong troubleshooting skills to assist with defining problems, collection of data, establishment of facts, and drawing valid conclusions
