Job Description:
1. Comply with GLP regulations and cooperate with the project leader to participate in in in vivo drug analysis and pharmacokinetic studies of small molecule chemical drugs;
2. Develop and validate drug LC-MS analysis methods in a GLP environment; Complete biological sample analysis and data QC work, assist the project leader in writing the initial report draft.
3. After the emergence of new technologies, regulations or guidelines related to safety evaluation, timely update the technical system of our department and provide training for implementation personnel;
Application channel:
Click on "I want to apply" on the right to fill in personal information or send your application materials to hr@xinbo.cn
Major in drug analysis, pharmacokinetics, pharmacy, etc., with a research focus on the development of drug fractionation analysis methods, proficient in using liquid chromatography-mass spectrometry;