CQV Execution Lead Engineer Biopharma Facility

Fluor Corp

Singapore

On-site

AUD 171,000 - 256,000

Full time

9 days ago

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Job summary

Fluor Corp is seeking an Execution Lead Engineer for a major pharmaceutical CQV project in Singapore. You will lead commissioning, qualification and validation activities across complex process and utility systems, coordinating EPCM contractors and vendors to deliver on safety, quality and schedule.

The role requires 10+ years in CQV, a Chemical/Mechanical/Process Engineering degree, and hands-on experience in GMP pharma/biotech environments.

Qualifications

  • 10+ years of experience in commissioning, qualification and validation (CQV) environments.
  • Experience with large-scale pharma/biotech manufacturing projects.
  • Hands-on CQV execution across complex process and utility systems.
  • Experience with Upstream/Downstream Processing Systems, CIP/SIP and GMP requirements.

Responsibilities

  • Lead commissioning and qualification execution from Mechanical Completion through system handover.
  • Execute CQV activities per approved execution plans and GMP requirements.
  • Support FAT preparation, witnessing and package readiness for equipment sourced globally.
  • Coordinate commissioning teams, vendors and calibration resources.
  • Prepare and support commissioning documentation including RAMS, PSSR, permits and method statements.
  • Lead system start-up, energisation and performance testing.

Skills

CQV execution
Commissioning engineering
Validation
GMP awareness
Stakeholder management

Education

Bachelor's degree in Chemical/Mechanical/Process Engineering

Tools

DCS
PLC

Job description

Fluor Corp is seeking an Execution Lead Engineer for a major pharmaceutical CQV project in Singapore. You will lead commissioning, qualification and validation activities across complex process and utility systems, coordinating EPCM contractors and vendors to deliver on safety, quality and schedule.

The role requires 10+ years in CQV, a Chemical/Mechanical/Process Engineering degree, and hands-on experience in GMP pharma/biotech environments.

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