Pharma Validation Officer

Prepare and execute validation protocols, procedures, and reports.

Perform process validation for pharmaceutical manufacturing operations.

Conduct equipment qualification, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).

Support cleaning validation to prevent cross-contamination.

Validate manufacturing equipment, utilities, and computerized systems as required.

Ensure compliance with GMP, SOPs, and applicable regulatory guidelines.

Review validation data and maintain accurate documentation.

Investigate deviations, discrepancies, and out-of-specification results related to validation activities.

Coordinate with Quality Assurance, Quality Control, Production, and Engineering departments.

Participate in audits, inspections, and regulatory compliance activities.

Monitor change controls and assess their impact on validated processes.

Maintain validation records and support periodic review and revalidation activities.