工作地点：中国上海外高桥保税区

Key accountabilities:
1.	Assist project PI in lab related activities, which include coordinating with sample manager, bioanalyst, instrument scheduling, report writer, QC/QA, etc. and filling out study documents.
2.	Plan and execute bioanalytical method development, method validation and perform analysis on samples from preclinical PK/TK studies and clinical trials.
3.	Troubleshoot technical and compliance issues occurred during method development or in-study phase.
4.	Process analytical data in Watson LIMS for acceptability of calibration curve, control values, test samples, and chromatograms.
5.	Write and review formal method of analysis, study report, and summaries relating to bioanalytical works.
6.	Function as QC to review the protocols, plans, sample treatment, data generation and reports relating to bioanalytical work.
7.	Assist the PI to ensure that projects are conducted within timeline and in accordance with applicable regulatory compliance. Keep project coordinator and PI informed on any study progress and issues. Monitor, track and provide resolution to all managed projects.
8.	Have an engaging and dynamic attitude towards rapid issue resolution and communication.

Requirements:
1.	BS, MS, PhD degree in a science discipline with experience or training in analytical chemistry, or equivalent experience.
2.	Execute and follow the policies and SOPs of BAS department and company. All work will be conducted in compliance with FDA Good Laboratory Practice regulation and OECD GLP guidelines.
3.	Be expected to perform the job independently with limited supervision form management. Must be customer-oriented and able to show flexibility and quick responsiveness in moving from one project to another. Qualified individuals will assist in other job functions on an as-needed basis.
4.	Be expected to accomplish their work assignments by interacting closely with fellow method development scientists and by developing cooperative working relationships with other personnel inside the company. 
5.	Be expected to be a supervisor and train junior employees.
6.	Open exchange of information and project teamwork will be required in order to meet performance. There must be strong recognition of high performance standards and of meeting assignment target dates at the individual job level as well as for the benefit of coworkers on project teams.
7.	Desired to have been trained in or have experience with the requirements of FDA GLP regulation and OECD GLP guidelines.
8.	Must be experienced with standard analytical techniques, particularly HPLC and LC-MS.
9.	Strong communication skills, both written and verbal, and outstanding interpersonal skill are essential job requirement.
10.	Must be able to openly share information and work in a team-oriented manner in order to accomplish performance objectives.
11.	Have passed proficiency test for bioanalyst.