- Prepare and maintain QC documents and records.
- Review SOPs, STPs, specifications, and analytical reports.
- Handle document issuance, control, and archival.
- Maintain laboratory logbooks and raw data records.
- Prepare Certificate of Analysis (COA).
- Ensure compliance with GMP and GLP guidelines.
- Review laboratory documentation for accuracy and completeness.
- Maintain calibration and instrument usage records.
- Support internal and external audits.
- Handle deviation, OOS, CAPA, and change control documentation.
- Coordinate with QA and QC departments for document updates.
- Ensure proper data integrity and confidentiality.
- Maintain documentation tracking registers.
- Organize and file quality-related records systematically.
- Ensure timely retrieval of documents when required.
- Monitor document revision and version control.
- Maintain electronic and manual documentation systems.
- Assist in preparation of regulatory documents.
- Follow company quality policies and procedures.
- Ensure all records are signed and completed properly.
Pay: ₹10,000.00 - ₹16,000.00 per month
Work Location: In person
