CQV Engineer – HVAC

QCS Staffing; Singapore; On-site; SGD 90,000 - 130,000; Full time

Job summary

QCS Staffing is seeking a CQV Engineer to join a Singapore-based Life Sciences project for a 24-month contract. You will develop and document IQ, OQ, and PQ for HVAC and cleanroom systems in GMP facilities, ensuring regulatory compliance across AHUs, HEPA filtration, ductwork, and environmental controls.

You will conduct smoke studies, airflow testing, and mapping, and coordinate with QA, Engineering, Operations, and Contractors to drive successful commissioning and requalification activities.

Qualifications

• Bachelor's Degree in Mechanical Engineering, Chemical Engineering, Building Services or related technical discipline.
• Extensive HVAC/Cleanroom CQV experience in pharma/life sciences environments.
• Strong understanding of GMP/ISO standards and GDP.

Responsibilities

• Develop, execute, and document IQ, OQ, and PQ protocols for HVAC and cleanroom systems in GMP facilities.
• Qualify AHUs, HVAC systems, HEPA filtration, ductwork, environmental controls, and Grade C/D cleanrooms for regulatory compliance.
• Conduct smoke studies, airflow tests, velocity testing, air-change calculations, HEPA integrity checks, particle monitoring, and temperature/humidity mapping.
• Coordinate with QA, Engineering, Operations, and Contractors; support FAT, SAT, commissioning, requalification, deviation management, and change controls.

Skills

Technical writing

Stakeholder management

Problem-solving

Independent work

Education

Bachelor's degree in Mechanical Engineering, Chemical Engineering, Building Services

Job description

CQV Engineer – HVAC – Singapore – 24-Month Contract – Life Sciences

How would you like the opportunity to work with in one of the largest biopharmaceutical projects in the country? If yes, then this is the assignment for you!

How would you like the opportunity to work with in one of the largest biopharmaceutical projects in the country? If yes, then this is the assignment for you!

Our client is currently seeking the skills of a CQV Engineer to join their team. Our client develops and delivers life changing medicines to millions of people globally and as part of their growth. With their Drug Substance (DS) manufacturing network growing rapidly, they are committed to growing their portfolio of commercial biologics products supplied worldwide – and this is your opportunity to be involved!

What You’ll Deliver

• Develop, execute, and document IQ, OQ, and PQ protocols for HVAC and cleanroom systems in GMP-regulated facilities.
• Qualify AHUs, HVAC systems, HEPA filtration, ductwork, environmental controls, and Grade C/D cleanrooms to ensure compliance with regulatory requirements.
• Conduct and assess smoke studies, airflow and velocity testing, air change calculations, HEPA integrity testing, particle monitoring, pressurization checks, and temperature/humidity mapping.
• Participate in FAT, SAT, commissioning, requalification, deviation management, change controls, and coordinate with QA, Engineering, Operations, and Contractors to ensure successful project execution.

Experience required:

• Bachelor's Degree in Mechanical Engineering, Chemical Engineering, Building Services, or a related technical discipline.
• Extensive HVAC/Cleanroom CQV experience within pharmaceutical, biotechnology, or life sciences manufacturing environments.
• Strong understanding of EU GMP Annex 1, ISO 14644 Cleanroom Standards, ISPE Baseline Guides, and Good Documentation Practices (GDP).
• Excellent technical writing, problem-solving, stakeholder management, and the ability to work independently while maintaining a strong compliance and quality focus.