- Prepare and review QC documents, test reports, specifications, and SOPs.
- Ensure accurate and timely documentation of laboratory activities and test results.
- Maintain COA, logbooks, analytical records, and raw data as per GMP requirements.
- Review batch-wise analytical documents for completeness and compliance.
- Support OOS, deviation, change control, and CAPA documentation.
- Ensure proper data integrity and Good Documentation Practices (GDP).
- Maintain and archive QC records for traceability and regulatory requirements.
- Coordinate with QA, QC, Production, and other departments for document-related activities.
Preferred candidate profile
- B.Pharm/M.Pharm/M.Sc./B.Sc. in relevant discipline.
- 25 years of experience in pharmaceutical QC documentation preferred.
- Knowledge of GMP, GLP, GDP, SOPs, and data integrity.
- Experience in QC records, COA, logbooks, analytical reports, and documentation.
- Valuable MS Office/Excel and ERP skills.
- Strong attention to detail, accuracy, and document control.
- Good communication, coordination, and organizational skills.