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 valuable 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