CQV Engineer / Pharma / West / SGD 6,300!

Integrity Partners; Singapore; On-site; SGD 70,000 - 100,000; Full time

Job summary

Integrity Partners is seeking a CQV Engineer to plan, execute, and document CQV activities (IQ, OQ, PQ) for pharmaceutical facilities, utilities, and equipment. The role involves ensuring compliance with GMP, GAMP 5, and related guidelines, and supporting FAT/SAT, risk assessments, and troubleshooting during readiness stages.

You will collaborate with engineering, project, and quality teams to resolve validation issues on time and maintain rigorous documentation throughout the commissioning and

Qualifications

• CQV experience in pharmaceutical or biotech manufacturing settings.
• Familiarity with cGMP, GAMP 5 and validation lifecycle protocols.
• Hands-on exposure to validating clean utilities (WFI, clean steam, HVAC), cleanrooms, or process equipment.

Responsibilities

• Plan, execute, and document CQV activities (IQ, OQ, PQ) for facilities, utilities, and equipment.
• Ensure documentation adheres to GMP, GAMP 5, ISPE Baseline Guides, FDA/EMA/PIC/S guidelines.
• Support FAT, SAT, risk assessments, and technical troubleshooting during equipment setup and readiness stages.
• Collaborate with engineering, project, and quality teams to drive execution and resolve validation issues on time.

Skills

CQV Experience

GAMP 5

cGMP

Validation Lifecycle

Education

Engineering or Life Sciences degree

Job description

My client is looking out for a CQV Engineer that has the following attributes:

Key Responsibilities

• CQV Protocol Execution: Plan, execute, and document CQV activities (IQ, OQ, PQ) for pharmaceutical manufacturing facilities, utilities, and process equipment.

• Compliance & Standards: Ensure all documentation and activities strictly adhere to GMP, GAMP 5, ISPE Baseline Guides, and FDA/EMA/PIC/S guidelines.

• Testing & Troubleshooting: Support FAT, SAT, risk assessments, and technical troubleshooting during equipment setup and operational readiness stages.

• Cross-Functional Collaboration: Partner with engineering, project, and quality teams to drive execution and resolve validation issues on time.

Requirements

• Degree in Engineering, Life Sciences, or a related discipline.

• 2–5 years of CQV experience within the pharmaceutical or biotech manufacturing sector.

• Practical knowledge of cGMP, GAMP 5, and validation lifecycle protocols.

• Hands-on experience validating clean utilities (WFI, clean steam, HVAC), cleanrooms, or process equipment.