Senior CQV Engineer - Facilities, Utilities & HVAC

EFOR (formerly Process Engineering Specialists)

Singapore

On-site

SGD 90,000 - 130,000

Full time

2 days ago
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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 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

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