Job Responsibilities:

1. Participate in the compilation of new product development requirements and assist the R&D team in conducting new product development;

2. Responsible for writing technical documents for medical device products, including product technical requirements, design and development documents, risk management reports, etc;

3. Responsible for the liaison work of engineering changes and the editing of related materials;

4. Daily communication and collaboration with regulatory registration department, business department, testing center and other departments;

5. Participate in responding to internal and external audits, and follow up on the technical department's rectification of non compliant projects.

Job Requirements:

1. Bachelor's degree or above, majoring in materials science, medicine, pharmacy, mechanical engineering or related fields;

2. Good English listening, speaking, and writing skills;

3. Have good skills in writing technical documents and registration materials;

4. Good internal and external communication and coordination skills, able to timely coordinate and solve various problems in registration;

5. Priority will be given to those with experience in R&D and registration of three types of medical devices.