Responsibilities:
1. Be involved in the project initiation, market demand analysis, design input and other work in the pre product period;2. Responsible for the structure design and development of new products, and complete the drawing, production assembly, test validation and product optimization;
3. Complete the design output (technical requirements, drawings, process flows, test methods, etc.) according to the design and development process of medical devices;
4. Responsible for risk management activities related to product design (hazard analysis, DFMEA, etc.);
5. Participating in a series of product verification activities, including design verification, animal experiment, and type inspection;
6. Responsible for the design improvement of tooling, equipment, fixture and so on in the production activities of products.
7.Complete the other work arranged by the leader.