Job Description：

1. Develop GMP certification work plans, inspection plans, and guide implementation;

2. Organize the preparation of GMP documents and be responsible for leading revisions or reviews;

3. Organize and coordinate the implementation of GMP preparation work and follow up on work plans;

4. Hosting the company's GMP certification training and specialized GMP certification meetings;

5. Regularly report GMP certification work to the company's GMP leadership group;

6. Organize the company's GMP certification self inspection work and write self inspection reports;

7. Responsible for regularly communicating with the National Medical Products Administration, the Certification Center, the Provincial Medical Products Administration, and GMP experts to effectively promote the company's GMP certification work;

8. Develop an annual verification work plan and participate in writing verification plans;

9. Assist superiors in establishing and improving the quality management document system, and supervise and inspect the implementation of the document system.

Job requirements：

1. Bachelor's degree or above in biomedical, pharmaceutical, or other related fields;

2. More than three years of work experience in this position, with experience in ophthalmology, surgical collagen, and cosmetics being preferred;

3. Familiar with medical device laws and regulations, ISO13485 standards, and GMP standards.