Day-to-Day Responsibilities
Write validation master plans and protocols for equipment, utilities, processes and cleaning
Run IQ, OQ and PQ (installation, operational and performance qualification) and record the results
Review validation data and investigate failures, raising deviations and CAPA where needed
Check that batch-level process parameters stay within validated limits during commercial production
Prepare validation files and support audits by US FDA, EU, WHO and Indian regulators
Revise procedures and re-validate after equipment changes, new products or technology transfer
Coordinate with production, QA, engineering and maintenance teams to schedule validation runs


