Hyderabad

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Key Responsibilities
- Lead the IPQA team and oversee in-process quality assurance activities across production (OSD / Injectable / Sterile / Packaging as applicable).
- Ensure line clearance is performed and documented before and after manufacturing and packaging operations.
- Monitor critical process parameters and in-process controls to ensure compliance with approved BMR/BPR and SOPs.
- Review and approve batch manufacturing and packing records, logbooks, and related GMP documentation.
- Ensure compliance with cGMP, GDP, ALCOA+ principles, and regulatory requirements (USFDA, EU GMP, WHO, MHRA).
- Coordinate with Production, QC, Engineering, Warehouse, and Validation teams for smooth manufacturing operations.
- Lead deviation investigations, root cause analysis, and CAPA implementation related to IPQA observations.




- Ensure timely escalation of critical quality issues and recommend appropriate corrective actions.
- Conduct GMP audits, floor walkthroughs, and ensure audit readiness of manufacturing areas.
- Review change controls, validation protocols, and qualification activities impacting production quality.
- Ensure data integrity compliance across production and quality systems.
- Train and mentor IPQA executives and officers on GMP compliance and quality standards.
- Participate in regulatory inspections, customer audits, and internal quality audits.
- Drive continuous improvement initiatives in quality systems and manufacturing compliance.
- Prepare and review quality metrics, trend analysis, and management review reports.
- Location Hyderabad
- Website [email protected]
- Salary Best in Industry
- EXPERIENCE NEED

📌 (QA) IPQA-Manager (Hyderabad)
🏢 KeyBiz Dashboards
📍 Hyderabad