**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** Familiar with SOPs, bioanalytical related regulations. Review the study related files, including plan, amendment, addendum, method and RQH, etc. Review the all the experiment records including study notebook, benchsheets, raw data, data processing and reports according to the SOPs and study plan. Periodically review all the laboratory instrument logbooks and maintenance documentations. Other assignments if needed. **Qualifications:** + Bachelor’s degree in a relevant scientific discipline (e.g., Biology, Chemistry, Biochemistry) or equivalent experience. + Familiar with Good Laboratory Practices (GLP) and regulatory requirements. + Ability to work independently and as part of a team. + Proficiency in data analysis and interpretation. + Good at English reading and writing. + Good at working with Microsoft software, eg. Excel, Word, ect. + 1-2 years bioanalytical experience, vaccine related experience better. Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.