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