CQV Commissioning Engineer Utilities

1 week ago

Galway, Galway, Ireland Steripack Full time

CQV Equipment Engineer – Utilities (Sterile Drug Product Facility)
Location:Dublin
Sector: Biopharmaceutical | Commissioning & Qualification
Type: Contract| On-Site

We are currently seeking a CQV Equipment Engineer – Utilities to join a high-performing team at a leading pharmaceutical facility in Dublin. This role focuses on the commissioning and qualification of utility systems within a state-of-the-art Sterile Drug Product (SDP) facility.

Key Responsibilities:

  • Prepare and execute CQV protocols for black utilities (e.g., compressed air, plant steam, chilled water, process waste)

  • Ensure all utilities are tested in compliance with GMP, EU/FDA regulations, and internal procedures

  • Support FATs/SATs, field inspections, and system walkdowns

  • Manage deviations and implement risk-based CQV strategies

  • Collaborate closely with vendors, site stakeholders, and contractors

  • Deliver documentation and training in line with project timelines and quality standards

What We're Looking For:

  • Degree in Engineering, Science, or a related technical field

  • 5+ years' experience in pharmaceutical CQV with a focus on utility systems

  • Proven experience across the full CQV lifecycle, from design through handover

  • Strong understanding of integrated automation in sterile manufacturing environments

  • Excellent communication, planning, and documentation skills

This is an excellent opportunity to work on cutting-edge projects in a global pharmaceutical environment, contributing directly to the launch-readiness of key manufacturing systems. To apply, please send your CV to

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