Quality Control Data Reviewer

Full-time Pharmaceutical Manufacturing

Responsibilities:

1. Capable of operating chromatographic software such as Waters Empower 3，Agilent CDS 2.
2. Familiar with Analytical Lab procedures, capable of identifying various errors in the analytical records.
3. Conduct the review of analysis methods, testing plans, experimental record calculations and data integrity strictly in accordance with relevant SOPs.
4. Timely report the identified errors in reviewing to ensure GMP compliance.
5. Follow the requirements of Lab events, OOX, Deviation and involve the investigation if necessary.
6. Involve in the procedure update and ensure procedure execution.
7. Assist the Lab management, ensure good Lab condition, ensure 5S compliance, sure Lab safety and the safety of Lab staff.
8. Proactively study regulatory documents from various countries, such as BP, USP, JP, and EP, and refer to these documents when updating internal procedures.
9. Assist th...