Raju Nagavath
Drug Inspector @Central Drugs Standard Control Organization
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WORK HISTORY
Drug Inspector @Central Drugs Standard Control Organization
Supported 15+ GMP inspections of sterile manufacturing sites, identifying early compliance gaps and enabling timely corrective actions to prevent regulatory escalation and supply disruption.Reviewed 60+ CAPA cases, strengthening batch release governance, investigation quality, and overall inspection readiness.Coordinated 12+ Special Expert Committee (SEC) meetings, enabling faster, risk-based regulatory decisions aligned with patient safety and product quality.Assessed data integrity, cleaning and sterilization validation, and contamination investigations, escalating significant quality risks to senior leadership for appropriate action.
EDUCATION
JNTUH College of Engineering Hyderabad
Bachelor's degree, Pharmacy
ABOUT RAJU NAGAVATH
Senior regulatory and quality professional with 12+ years of experience in aseptic pharmaceutical manufacturing, GMP compliance, and regulatory oversight across pharmaceuticals, biologics, and medical devices.Currently working within a national regulatory authority, responsible for scientific review, compliance assessment, and inspection readiness of high-risk products and manufacturing facilities, ensuring alignment with EU and WHO GMP standards.Brings strong hands-on experience in sterile injectable manufacturing, including aseptic filling, media fills, environmental monitoring, contamination investigations, process validation, and CAPA management. Combines industry execution with regulatory evaluation to identify compliance risks early and implement sustainable, science-based quality solutions.Successfully qualified the highly competitive UPSC Drugs Inspector examination and all-India interview, reflecting strong expertise in regulatory science, pharmaceutical law, GMP, and public health protection.Committed to patient safety, data-driven decision-making, and inspection-ready quality systems.
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