Validation Engineer

Job Description

Job Description

We are seeking a CQV Engineer to support and lead qualification efforts for facilities, utilities, and equipment in a regulated manufacturing environment. The successful candidate will focus on ensuring systems are commissioned, qualified, and validated in compliance with cGMP standards and regulatory requirements.

Responsibilities :

• Lead qualification activities for cleanrooms, HVAC systems, and utilities such as purified water, compressed air, and gas systems.
• Conduct system walk-downs, verify P&IDs, and address deficiencies or deviations identified during qualification.
• Author and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols for manufacturing and laboratory equipment, including autoclaves, cryogenic freezers, and biosafety cabinets.
• Oversee validation testing to ensure compliance with regulatory standards and operational requirements.
• Prepare comprehensive qualification protocols, validation summary reports, and traceability matrices in adherence to Good Documentation Practices (GDP).
• Maintain organized and timely records to meet both internal and external audit requirements.
• Execute system testing using tools such as thermocouples, pressure sensors, and data loggers.
• Identify and resolve issues during commissioning and qualification phases.
• Work closely with project teams, including Quality Assurance, Operations, and Engineering, to ensure alignment on validation objectives.
• Support cross-functional teams during audits and regulatory inspections as a subject matter expert (SME) for CQV processes.

Requirements

Qualifications

Benefits