Validation Engineer (MNC/pharmaceutical)

About this role

Key Responsibilities Execute CQV activities for GMP-regulated pharmaceutical and biopharmaceutical facilities. Prepare and review validation documents, including plans, IQ/OQ/PQ protocols, test scripts, and reports. Support validation of equipment, utilities, facilities, and computerized systems in

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• Building and Construction
• FDA standards
• CAPA
• cGMP
• Environmental & Utilities

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