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About the Role
Develop and execute validation protocols for equipment, processes, and systems
Review and approve validation documentation and reports
Ensure compliance with WHO-GMP, FDA, and MHRA guidelines
Conduct validation of manufacturing equipment, utilities, and computer systems
Coordinate with cross-functional teams for validation activities
Requirements
Bachelor's degree in Pharmacy, Chemistry, or Life Sciences
Minimum 3-4 years experience in QA/Validation in pharmaceutical industry
Knowledge of validation protocols (IQ, OQ, PQ) and regulatory requirements
Experience with equipment, process, cleaning, and computer system validation
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