Job Responsibilities：
1. Write the technical requirements of medical device products, follow the registration inspection and obtain the registration inspection report;
2. Written, organize medical equipment registration application materials;
3. Medical equipment products are registered, followed by coordination and forensics.
4. Register the relevant documents to organize and archive;
5. Maintain good links with relevant departments of the Food and Drug Administration, closely follow the registration process and regulations;
6. Solve the problem proposed by the registration review process;
7. Other work assigned by the leadership;
Job requirements:
1. More than 2 years of medical equipment registration experience, active and passive medical equipment experience can be;
2. Technical and engineering professional background, medical, biological, electronics and other majors; 3. Proficiency in the common office software;
4. Level 4 or above, English literature reading, writing abilities, oral communication skills;
5. Good communication skills, agile thinking, clear mouthkeep, have a summary habit.
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