Catering subsidies Regular medical examination Professional training Five insurances and one housing fund Employee travel Year-end bonus Performance bonus

　　Job information

　　1. Organize the formulation of quality management system, post SOP and other documents, organize personnel in the department to prepare various business work plans, be responsible for holding business meetings within the department, and check the implementation of relevant work plans.

　　2. Be responsible for the quality audit of suppliers, and have the right to determine the quality of raw materials, intermediates and finished products.

　　3. Responsible for the review and handling of returned drugs and unqualified drugs.

　　4. Responsible for the quality supervision of the whole process of drug production.

　　5. Responsible for the review and approval of various inspection reports.

　　6. Responsible for the review of batch production records, and write criticisms for batch production records.

　　7. Responsible for organizing the regular quality upgrading plan of the workshop and participating in the drug quality analysis.

　　8. Responsible for reviewing the verification schemes of plant, equipment, process, water production, etc., and supervising the implementation.

　　9. Other matters arranged by the leader.

　　10. Experience in working as a QA supervisor in a pharmaceutical factory is preferred.