Job Responsibilities:
1. Coordinate the construction of software system for GMP certification of existing workshops and new pharmaceutical factories in the future, organize the preparation of software system data for GMP certification, and standardize the operation and management of the company according to GMP certification standards;
2. Responsible for the company's implementation and enforcement of drug production laws and regulations, responsible for the establishment of quality assurance management system and the organization of implementation;
3. Establish deviation treatment management system and review deviation treatment records. Responsible for organizing quality system evaluation of major material suppliers. Responsible for supervising the stability inspection of materials, products and intermediate products;
4. Responsible for implementing supervision and urging the completion of product quality review analysis report, and rectification of defects suggested by product quality review summary;
5. Responsible for personnel and organization training, personnel health management, plant and facilities, equipment, materials, public systems, production workshop, warehouse, quality control and other management.
Job Requirements:
1, Pharmacy or related major, bachelor degree or above;
2. Rich experience.