Job responsibilities:

1. Be responsible for the planning and preparation of the company's product registration materials and the registration and certification work;

2. Responsible for the collection and internal training of relevant regulations and standards of the medical device industry;

3. Participate in the establishment, improvement and operation of the company's medical device quality management system;

4. Keep effective communication with relevant testing institutions and review centers;

5. Complete other tasks assigned by leaders.

Job requirements:

1. Bachelor degree or above;

2. Materials and engineering, biomedicine, medical devices and other related majors;

3. More than 3 years of medical device registration experience, familiar with medical device regulations and quality management system;

4. Those with three types of passive implant medical device product registration experience are preferred;

5. Good written expression ability, communication and coordination ability, and excellent team spirit.