Job Responsibilities:

1. Carry out product registration and system certification, and apply for the replacement and replacement of certificates that have been obtained;

2. Follow up the collation and internal review of registration application materials throughout the process, submit application materials, and complete the relevant work of registration application and supplementary application;

3. Communicate with the government and relevant industry departments on registration matters, coordinate and deal with problems arising in the registration process, and ensure that registration approvals are obtained on time;

4. Review the declaration work;

5. Filing and sorting of registration materials and original records;

6. Assist in other matters arranged by the department.

Request:

1. Bachelor degree or above in medicine, nursing, foreign language and other majors;

2. Have certain experience in medical device product registration;

3. Able to withstand certain working pressure;

4. Strong English listening, speaking, reading and writing skills.