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.