1、Responsible for the operation and management of quality systems such as deviations and CAPA, establishing ledgers and tracking the progress of each of the above until closure.

2、To guide other department personnel in the above related quality matters and be able to evaluate and audit the results efficiently.

3、Be responsible for annual reviews of the operation of systems such as deviations, CAPA, etc.

4、Participate in official and/or third party audit activities of the company and cooperate in providing metrology related documents and records during audits and provide answers when necessary.

5、Complete other tasks assigned by the supervisor.

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

2、2 years of relevant work experience in pharmaceutical companies. Preferably with quality work experience in biopharmaceutical companies

3、Familiar with the operation of word, excel and other common office software.

4、Have basic English reading and writing skills.

5、Strong risk awareness and problem analysis and judgment, communication and coordination skills and writing skills, including data analysis, investigation and research and report writing

6、Ability to use quality management tools proficiently.