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 jobs@forcerecruitment.com
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