1、Experience in HCP residue, Protein A residue, DNA residue, binding activity and cellular activity and other related assays.
2、Can draft instrumentation SOP, test method SOP, validation program and validation report and other documents.
3、Familiarity with assay instruments such as enzyme markers and qPCR instruments.
4、Ensure that daily behavior and operation can be fully in accordance with the requirements of GMP.
5、Responsible for the cleaning, maintenance and upkeep of relevant instruments in the laboratory, and assist QA to complete the calibration of instruments.
6、The deviations, AD/OOS/OOT problems that occur during the testing process can be reported to the superior leadership in a timely manner, and complete the relevant investigations.
7、Complete the tasks explained by the superior leadership.

1、College degree or above, majoring in medicine or biology related majors, with relevant workers preferred.

2、Preferably with GMP related experience and knowledge background.

3、Have good behavioral habits, strong anti-stress ability and good communication skills.