Job Description:
Responsible for on-site QA supervision, including material, production, QC laboratory, drug registration and development, and other on-site quality management. Participate in auditing suppliers. Assist in investigating changes, deviations, OOS, and complaints caused by quality issues, supervise the implementation of CAPA, and investigate and analyze any adverse trends found in the production quality management process. Assist in organizing internal/external audits, receive certification department audits and inspections, and implement corrective actions for non conformities. Organize inspections of company quality management issues and participate in the preparation of various product quality reports.
Job requirements:
Under 35 years old. Graduated from a major in chemistry, pharmacy, or related fields, with a bachelor's degree or above.
Work location: Shanghai Songjiang, Anhui Chizhou Dongzhi Economic Development Park