Responsibilities：
1. Development and validation of quantitative LC-MS/MS method for analysis of drugs，metabolites, biomarkers in biological matrices.
2. Conducting routine sample analysis for pre-clinical and clinical studies in compliance with GLP.
3. Record-keeping in compliance with GLP.
4. Preparation of study protocols, analytical procedures and reports.
Requirements:
1. Chemistry, analysis, bioanalysis, or pharmacology background.
2. Hands-on experience on LC-MS/MS implementation, validation, and sample analysi.
3. GLP work experience is a plus.
4. Ability to read, write and speak English.
5. Must be able to work in a dynamic working environment.
6. Good communication skill.