Key Responsibilities: • Plan, execute, and document validation activities for QC laboratory equipment, methods, and systems (IQ/OQ/PQ). • Perform routine calibration, verification, and preventive maintenance of analytical instruments. • Review and approve validation protocols, reports, and SOPs in compliance with GMP standards. • Conduct troubleshooting and root cause analysis for equipment and method deviations. • Support method transfer, technology implementation, and regulatory inspections. • Collaborate with cross-functional teams (QC, QA, Production) to ensure data integrity and process reliability. • Maintain accurate and compliant records in line with company and regulatory requirements.