- Review HPLC analytical data, chromatograms and results.
- Review analytical worksheets, calculations and raw data.
- Ensure analysis is performed as per approved SOPs and specifications.
- Review and verify analytical documentation for accuracy and completeness.
- Coordinate with QC analysts for any discrepancies or corrections.
- Handle OOS/OOT and analytical investigations as required.
- Ensure compliance with GMP, GLP and data integrity requirements.
- Support internal, customer and regulatory audits.
Qualification M.Sc /B.Sc or relevant qualification.
Requirements
- 3–6 years of relevant experience in Formulation QC.
- Robust experience in HPLC analysis and data review.
- Good knowledge of GMP, GLP and data integrity.
- Pharmaceutical formulation experience preferred.