1. Be responsible for the registration management of active medical devices;

2. Be responsible for technical regulation support of active device product registration.

1. Bachelor degree or above, major in clinical medicine, biology, biopharmaceutics, materials science, etc;

2. Skillfully use various office software and office equipment;

3. Proficient in medical device product registration process, able to independently organize the review of medical device related registration materials, and complete the registration work;

4. Familiar with national policies and regulations on medical device registration; Understand ISO9000, ISO13485, GMP and other quality management systems and production knowledge;

5. Good team cooperation and execution ability, coordination ability, analysis and response ability, communication ability, interpersonal skills.