1.Responsible for the testing and report writing of our pre-clinical biological samples.
2.Responsible for the routine testing of toxic species products.
3.Responsible for the routine testing of CMC products for small trials.
4.Responsible for the daily management of testing reagents, consumables and instruments.
5.Participate in the formal validation of bioanalytical assays.
6.Participate in the development and continuous optimization of bioanalytical assays.
7.Participate in the validation program and validation report writing, review and implementation.
8.Participate in the management and reassessment of all internal standards and key reagents in the department.
9.Participate in the writing of SOPs, reports, ROA, etc., and archiving of experimental reports and other documents in the department.
10.Complete other work as assigned by the supervisor.
1.Bachelor's degree or above, majoring in biology/virology/pharmacology/basic medicine/etc., with bioanalytical-related internship experience is preferred.
2.Familiar with relevant experimental skills such as ELISA, qPCR, cell culture, etc., and familiar with the operation of relevant graphing and analysis software such as Excel, Graphpad, etc.
3.Strong analytical and problem-solving skills. Strong logical thinking, keen insight, and strong learning ability. Communication and coordination skills and team spirit.
4.Have some English reading and writing skills.