Validation engineer

Job Title

Key Responsibilities

• Execute Facilities CQV activities, including EMPO, Vessel IOV, and IOPQ (mixing and temperature mapping).
• Support commissioning and qualification of process equipment such as centrifuges, filter presses, and processing tanks.
• Perform installation qualification (IQ) and operational qualification (OQ) of equipment and systems.
• Conduct job walks at the construction site with engineering teams to monitor progress and compliance.
• Collaborate with cross-functional teams to ensure project timelines and quality standards are met.
• Generate, review, and maintain technical documentation for CQV deliverables.
• Provide additional support for systems such as Utilities (WFI, Alcohol, N, Compressed Air), CIP, Filter Press, Centrifuge, and Cleaning Validation as needed.
• Maintain high safety standards while performing daily activities in a regulated environment.

Qualifications

• Bachelor's degree in Engineering or a related field.
• 3-10 years of experience in Validation or CQV within the pharmaceutical industry.
• Strong knowledge of facilities and process equipment validation.
• Cleanroom qualification experience is a plus.
• Excellent technical writing and documentation skills.
• Strong communication, organization, and multitasking abilities.
• Experience supporting capital projects and conducting job walks.
• Must be flexible to support other shifts on short notice as required.
• Local candidates preferred.