Description
Job SummaryYou will be responsible for the development and design aspects in the Design Control and Technical Documentation. You might be in the position to lead Projects of small groups.
For my client in the North-Central part of Switzerland I am searching a DHF Consultant / Development Engineer. The project is planned for 2 month, min. 40 hours a week.
Duties and responsibilities
- Design Control of complete Project assignments
- Implementation of technical standards and coordination with other departments
- Participates in root cause analysis for problem solving
- Prepare protocols for product testing and analysing
- Preparation of existing (modification) and new product specification's
- Design assurance documentation for the product
Requirements
- Bachelor in Mechanical Engineering or Biomedical Engineering or similar
- 3 + years of experience in Medical Devices / Experience with the ISO 13485
- Working Experience in following areas: Medical Devices, design control, FDA QS-regulations, product development
- Solution orientated by using modern technology
- Knowledge/ Understanding of Standards acc ISO 13485 and the Implementation
- Professional communication skills
- English business fluent spoken and written
For more information on this or other opportunities contact Marco Heumann, at Real Staffing Group, Zürich