Job Responsibilities:
1. Responsible for quality monitoring and release approval of raw materials and intermediate products;
2. Responsible for inspecting the implementation of production process discipline in each workshop and reviewing batch production records;
3. Verify that the quality of raw and auxiliary materials, intermediate products, and finished products complies with process requirements; for any nonconforming raw and auxiliary materials or intermediate products, you have the authority to prevent their transfer to the next production stage.
4. Promptly notify workshop management of any abnormalities occurring on the production floor, collaborate with the workshop to investigate the root causes of deviations, and closely monitor the implementation of corrective actions for all types of deviations.
5. Supervise that finished goods are received into inventory in accordance with requirements and monitor the destruction of nonconforming products;
6. Supervise and inspect the implementation of process change and equipment change procedures;
7. Participate in the quality assessment of key material suppliers, track and provide feedback on the quality of materials used in the production process, and conduct GMP self-inspections at the production site, as well as supervise and inspect the implementation of corrective actions and improvements.
Job Requirements:
1. Bachelor’s degree or higher in Pharmacy or a related field;
2. Strong organizational and execution skills, with a solid team-player mindset and excellent communication abilities; highly responsible.
3. Candidates who have received training in GMP and pharmaceutical regulatory laws and regulations, and who have work experience in production operations, quality management, or validation, will be given priority.
