CQV Engineers-Facilities & Utilities/Process Equipment/HVAC(Multiple Roles)

EFOR (formerly Process Engineering Specialists); Singapore; On-site; SGD 90,000 - 130,000; Full time

Job summary

PES is an international services company delivering CQV services to pharmaceutical, nutritional, and related sectors. With offices across Europe, Asia and the US, we focus on delivering high-quality outcomes for multinational clients.

We are currently looking for Leads/Seniors/Engineers to join us permanently and deliver CQV projects in the Life Sciences Industry. This role involves leading CQV activities across facilities, process equipment, and HVAC domains, with emphasis on IQ/OQ/PQ and GMP

Qualifications

• Develop and review CQV lifecycle documents (URS, IQ/OQ/PQ protocols).
• Author validation protocols and reports per site procedures and regulatory expectations.
• Maintain document formatting, version control, and traceability.
• Collaborate with CQV engineers, QA and project stakeholders on inputs.
• Support revisions, approvals and close-out to meet timelines.
• Ensure documentation aligns with GMP, Annex 15 and site quality systems.

Responsibilities

• Develop and review CQV lifecycle documents, including URS, DQ summaries (as applicable), IQ, OQ, and PQ protocols and reports
• Author validation protocols and reports in accordance with site procedures and regulatory expectations
• Ensure proper document formatting, version control, and traceability throughout the document lifecycle
• Coordinate with CQV engineers, QA, and project stakeholders to gather and verify technical inputs
• Support document revisions, approvals, and close-out activities to meet project timelines
• Ensure documentation aligns with GMP (EU/FDA), Annex 15, ASTM E2500, and site-specific quality systems
• Maintain audit-ready documentation by ensuring completeness, accuracy, and compliance
• Track documentation status and support timely delivery of validation deliverables
• Assist in risk assessments, traceability matrices (RTM), and change control documentation
• Collaborate with cross-functional teams including Engineering, QA, Automation, and external vendors

Skills

CQV Engineering

Life Sciences

Document control

Regulatory compliance

IQ/OQ/PQ

Job description

PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.

With offices across Europe, Asia and US, our core focus is on consistently delivering high quality outcomes for our multinational clients.

This focus and our people's experience in delivering consistent quality results for our clients over the past 20 years have been key to our success to date.

We are currently looking for CQV engineers to join us permanently to help us deliver various projects in the Life Sciences Industry.

We are looking for the following Leads/Seniors/Engineer:

• Facilities & Utilities
• Process Equipment
• Clean Air Devices / HVAC

Key Responsibilities:

• Develop and review CQV lifecycle documents, including URS, DQ summaries (as applicable), IQ, OQ, and PQ protocols and reports
• Author validation protocols and reports in accordance with site procedures and regulatory expectations
• Ensure proper document formatting, version control, and traceability throughout the document lifecycle
• Coordinate with CQV engineers, QA, and project stakeholders to gather and verify technical inputs
• Support document revisions, approvals, and close-out activities to meet project timelines
• Ensure documentation aligns with GMP (EU/FDA), Annex 15, ASTM E2500, and site-specific quality systems
• Maintain audit-ready documentation by ensuring completeness, accuracy, and compliance
• Track documentation status and support timely delivery of validation deliverables
• Assist in risk assessments, traceability matrices (RTM), and change control documentation
• Collaborate with cross-functional teams including Engineering, QA, Automation, and external vendors

PES International operates as an equal opportunity employer. No terminology in this advert is intended to discriminate on the grounds of age, race, religion, sexual orientation or any other factors with no bearing to employment skills and we confirm that we are happy to accept applications from persons of any background for this role.