Responsibilities: management of the GMP documents and records; such as distributing; returning, replacing or revoking, copying, archiving and canceling; the writing, applying, sampling, sample-sealing, sample-sending of lot release summary and the obtaining and distribution of lot release reports; investigation, evaluation, grade, and treatment of offsets, changes, CAPA, form related measures and trace them; organize company self-inspection, monitor the self inspection of departments and achive related materials, participate in outer auditing; collect information about retrospective quality review and write annual retrospective quality review; products-recall and related work; monitor the training of the company; other work arranged by mangers. 

Qualification: pharmacy-related major, college degree or above; those people with more than 1 year of drug-producing or quality management experience is preferred; Serious and careful working attitude, be active and hardworking during working period, have a sense of safety, obey the arragement of leaders; be proficient in office software, good ability of communication and excellent execution. 

Welfare: social insurance and housing bonus; perfect attendance bonus; 8-hour work; holiday welfare; free working meal; physical examination.