1, to assist the department head to carry out internal and external quality audit, do a good job of laboratory preparation before external quality audit;

2. Responsible for laboratory compliance inspection, notification and rectification tracking;

3, responsible for R & D related inspection and acceptance review;

4, responsible for laboratory measurement calibration management;

5, responsible for improving the computerized management of the laboratory, the three-level authority of instruments and equipment and the supervision and implementation of data backup;

6. Responsible for the management of self-made antigens and antibodies for research and development purposes;

7, responsible for the daily sampling of experimental records, turnover verification, special sampling management;

8. Other work related to verification and audit。

1. Master degree or above in biotechnology, bioengineering, biopharmaceutical or pharmacy related field。

2, familiar with drug related policies and regulations (GMP or GLP, etc.) requirements;More than 1 year on-site audit, self-audit (internal audit) related work experience, have passed the drug regulatory department audit is preferred。

3, have a certain ability of text editing, work organized, careful, patient。Good team spirit and rigorous work attitude。