1、Responsible for the audit and communication in the process of signing quality assurance agreements for each project.

2、Responsible for the communication in the process of customer audit of each project, the development of rectification plan and the issuance of rectification report.

3、Responsible for the handling of deviations, changes, CAPA, etc. during the project operation, as well as the communication with customers on related contents.

4、Participate in project meetings and answer questions on quality system.

5、According to the project requirements, organize and provide the corresponding information.

1、Bachelor degree or above in pharmacy, biology or related majors.

2、Understanding of pharmaceutical production, testing and quality management, familiar with GMP regulations.

3、3 years and above relevant work experience in QA quality system of pharmaceutical companies.

4、Strong communication and coordination skills and writing ability.

5、Good English ability.