- Manage cleaning validation, equipment qualification, and validation documentation.
- Handle CAPA, change control, deviation management, and quality risk assessment.
- Conduct mock recall and mock audit activities as per approved SOPs.
- Manage dossier documentation and support regulatory submissions.
- Review calibration records and ensure timely calibration of instruments and equipment.
- Review raw material documentation, specifications, COA, and supplier-related records.
- Maintain and control GMP documentation, SOPs, protocols, reports, and quality records.
- Review stability data, stability protocols, and reports for API products.
- Ensure compliance with cGMP, data integrity, and positive documentation practices.
- Coordinate with Production, QC, Engineering, Warehouse, and Regulatory Affairs for QA activities.
- Support internal audits, customer audits, and regulatory inspections.

Pay: ₹250,000.00 - ₹350,000.00 per year

Work Location: In person

📌 QA Officer (Vadodara)
🏢 Livmore Life Sciences
📍 Vadodara