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.