Utilities Engineer – Life Sciences (cGMP) – Black Utilities

QCS Staffing

Roscommon

On-site

EUR 52,000 - 76,000

Full time

14 days+

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Job summary

QCS Staffing seeks a Utilities Engineer in Ireland, Roscommon, on an initial 12-month contract in the Life Sciences sector. The successful candidate will support delivery of the project, ensuring reliable operation and compliance of black utility systems within a cGMP environment.

You will lead CQV strategy and execution for black utilities (chilled water, LPHW, steam, compressed air), contribute to maintenance strategy handover, and work with regulated manufacturing facilities to meet GMP

Qualifications

  • Bachelor’s degree in Mechanical, Chemical, Electrical, or Process Engineering.
  • Extensive experience with industrial plant utilities in regulated environments (cGMP).
  • Experience supporting construction and commissioning on live sites.
  • Familiarity with GMP requirements in regulated manufacturing facilities.

Responsibilities

  • Ensure reliable operation, compliance and lifecycle management of black utility systems in a cGMP environment.
  • Monitor and improve system processes for efficiency, reliability and regulatory compliance.
  • Conduct risk assessments and develop mitigation strategies for utility systems.
  • Lead CQV strategy and execution for black utilities (chilled water, LPHW, steam, compressed air) and set handover requirements.

Skills

Regulatory compliance
Risk assessment
Process improvement

Education

Bachelor’s degree in Mechanical/Chemical/Electrical/Process Engineering

Tools

GMP awareness

Job description

QCS Staffing seeks a Utilities Engineer in Ireland, Roscommon, on an initial 12-month contract in the Life Sciences sector. The successful candidate will support delivery of the project, ensuring reliable operation and compliance of black utility systems within a cGMP environment.

You will lead CQV strategy and execution for black utilities (chilled water, LPHW, steam, compressed air), contribute to maintenance strategy handover, and work with regulated manufacturing facilities to meet GMP

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