Job information

　　1. Responsible for the management of the company's R&D quality system documents.

　　2. Responsible for the management of MAH related quality documents.

　　3. Responsible for the establishment and management of supplier files.

　　4. Responsible for the distribution and archiving of experimental books and auxiliary records.

　　5. Responsible for the review and archiving of the company's R&D project data.

　　6. Responsible for the review of drug quality standards and operating procedures.

　　7. Assist the superior to complete the review and archiving of the entrusted product batch records.

　　8. Responsible for the preparation of documents for the Food and Drug Administration, customer audit or registration verification.

　　9. Responsible for the regular review of the company's documents to ensure that the documents used meet the current requirements.

　　10. Responsible for the archiving of verification, confirmation, deviation, change, batch records, registration and other materials.

　　11. Coordinate relevant personnel in various departments to complete the drafting and revision of quality system documents.

　　12. Responsible for formulating the company's annual and quarterly training plans, assisting the office in organizing company training,

　　13. Responsible for formulating annual and quarterly training plans for the Quality Management Department, and organizing relevant training for the Quality Management Department according to the plan.

　　14. Responsible for the recovery and archiving of training records, and update personal training files on a quarterly basis

　　15. Responsible for formulating the annual quality review of commissioned products.

　　16. Assist superiors in quality system construction and continuous improvement.

　　17. Complete other tasks assigned by superiors.

　　Age requirement: 25-45 years old