Job Responsibilities:

1. Implement effective quality control over the entire process of all activities related to drug production such as warehouses, production workshops, and engineering;

2. Supervise and inspect the cleanliness of the production site;

3. Check the standardization and timeliness of various status signs;

4. Batch production records and various auxiliary records are issued, retracted, reviewed, and archived, and the timeliness, authenticity, and completeness of records are reviewed;

5. Responsible for the clearance inspection of each production site, and issue the clearance certificate;

6. Participate in the investigation, evaluation and treatment of deviations in the production process, and track the implementation of corrections and preventive measures;

7. Participate in the handling of changes and CAPA, track the implementation of corrections and preventive measures;

8. Statistical analysis of the quality data of each product, collection and trend analysis of annual review data of product quality;

9. Investigation and analysis of unqualified products, and follow-up implementation;

10. Accompanied by official or customer certification inspections, rectification and follow-up implementation

11. Responsible for the daily inspection of the company's quality system and organizing GMP self-inspection according to regulations;

12. Coordinate and cooperate with production, workshop, warehouse, engineering and other related quality conditions to ensure efficient and reasonable operation of the system;

13. Other tasks assigned by superiors;

job requirements:

1. Major in pharmacy, pharmaceutical engineering, chemistry, chemical engineering, college degree or above;

2. Two years and above QA work experience;