- Overall Quality Assurance
- Support day-to-day QA operations across Production, Quality Control, Warehouse, Packing and other departments.
- Ensure compliance with cGMP, SOPs and applicable regulatory requirements.
- Coordinate with departments to ensure adherence to established quality systems.
- Assist in identifying and resolving quality-related issues.
- Documentation & Quality Management Systems
- Review and maintain BMRs, BPRs, SOPs, logbooks and other GMP documentation.
- Assist in handling deviations, change controls, CAPA and other QMS activities.
- Support document control, issuance, review and archival activities.
- Assist in internal audits, regulatory inspections and compliance follow-ups.
- In-Process Quality Assurance (IPQA)
- Perform IPQA activities in manufacturing and packing areas as required.
- Conduct line clearance, in-process checks and verification of manufacturing activities.
- Monitor compliance with approved manufacturing procedures and documentation practices.
- Coordinate with Production and QC teams on in-process quality requirements.
- Cross-Functional Coordination
- Work with Production, QC, Stores, Packing and other departments on quality matters.
- Follow up on pending QA observations, documentation and compliance requirements.
- Assist with routine monitoring, reporting and continuous improvement initiatives.
- Undertake additional QA responsibilities assigned by the department head.
Qualification & Experience
- B.Pharm / M.Pharm / B.Sc. / M.Sc. in a relevant discipline.
- 2–5 years of Quality Assurance experience in pharmaceutical manufacturing.
- Working knowledge of GMP, pharmaceutical documentation and quality management systems.
- Exposure to manufacturing, packing and IPQA activities preferred.