Validation Engineer – Pharmaceutical Equipment

Responsibilities

• Plan and execute IQ, OQ, and PQ validation protocols for pharmaceutical equipment.
• Validate CIP/SIP systems, autoclaves, and fill-finish equipment.
• Prepare validation master plans, protocols, and summary reports.
• Support computer system validation (CSV) activities per GAMP 5 guidelines.
• Manage change controls and revalidation activities.

Requirements

• Degree in Engineering, Pharmaceutical Sciences, or related technical field.
• 3-5 years of validation experience in pharmaceutical manufacturing.
• Knowledge of EU GMP Annex 15, FDA process validation guidance, and ISPE guidelines.
• Experience with GAMP 5 and computerized system validation.
• Strong documentation skills and attention to regulatory detail.