HVAC & Grey Utilities CQV Engineer

CareerWise Recruitment; Limerick; On-site; EUR 60,000 - 90,000; Full time

Job summary

CareerWise Recruitment is seeking a CQV Engineer for grey utilities in Limerick, Ireland, to execute commissioning, qualification, and validation activities focusing on HVAC and related utilities.

The role requires 5+ years in CQV within a regulated pharmaceutical environment, with strong knowledge of GEP, cGMP, FDA, EMA and ISPE guidelines. Collaboration with project engineering, automation, production and quality teams is essential for success.

Qualifications

• Bachelor’s degree in Engineering or related technical field.
• Minimum 5 years’ CQV experience focusing on grey utilities in regulated pharma.
• Familiar with grey utility systems and ISPE/guidance.
• Experience preparing and executing CQV documentation and reports.

Responsibilities

• Plan, coordinate, and execute CQV activities for grey utilities.
• Prepare, review, and execute CQV protocols and reports (URS, FAT, SAT, IQ, OQ).
• Review design and installation documentation (P&IDs, datasheets, equipment lists).
• Interface with project engineering, automation, production, and quality teams.
• Support utility system start-up, troubleshooting, and post-commissioning optimization.
• Ensure compliance with cGMP, FDA, EMA, ISPE guidance.
• Coordinate with vendors and contractors for CQV execution.
• Participate in risk assessments (HAZOP, FMEA).
• Address deviations, CAPAs, and change controls as required.
• Maintain clear records of qualification activities and findings.
• Provide progress updates and participate in project meetings.
• Support training of operations and maintenance teams regarding qualified utilities.

Skills

CQV experience

Regulatory knowledge

Cross-functional collaboration

Documentation

Education

Bachelor’s degree in Engineering

Job description

CareerWise Recruitment is seeking a CQV Engineer for grey utilities in Limerick, Ireland, to execute commissioning, qualification, and validation activities focusing on HVAC and related utilities.

The role requires 5+ years in CQV within a regulated pharmaceutical environment, with strong knowledge of GEP, cGMP, FDA, EMA and ISPE guidelines. Collaboration with project engineering, automation, production and quality teams is essential for success.