Clean Utilities CQV Engineer

Black Diamond Networks; Limerick; On-site; EUR 60,000 - 90,000; Full time

Job summary

Black Diamond Networks is seeking an experienced Clean/Grey Utilities CQV Engineer to support commissioning, qualification, and validation activities at its site. The role involves planning and executing CQV protocols and reports for clean and grey utility systems, ensuring GMP, GEP, regulatory and site quality requirements are met.

The candidate will review engineering documentation, support FAT/SAT, manage deviations and punch-list items, coordinate with engineering, construction, quality and

Qualifications

• Experience in pharmaceutical or biotechnology CQV.
• Strong understanding of utility systems and validation principles.
• Excellent communication and documentation skills.

Responsibilities

• Plan and execute CQV protocols and reports for clean and grey utility systems.
• Review engineering documentation and specifications.
• Support FAT/SAT and commissioning activities.
• Manage deviations and punch-list items.
• Coordinate with engineering, construction, quality and operations teams.
• Maintain project records through to handover.

Skills

CQV

Commissioning

Validation

Documentation

Regulatory compliance

GMP

GEP

Job description

Job Description: The client is seeking an experienced Clean/Grey Utilities CQV Engineer to support commissioning, qualification, and validation activities at its site. The successful candidate will be responsible for planning and executing CQV protocols and reports for clean and grey utility systems, including purified water, clean steam, compressed gases, HVAC, process gases, wastewater, and associated plant utilities, while ensuring compliance with GMP, GEP, regulatory, and site quality requirements. The role will involve reviewing engineering documentation and specifications, supporting FAT/SAT and commissioning activities, managing deviations and punch-list items, coordinating with engineering, construction, quality, and operations teams, and maintaining accurate project records through to handover.

Requirements: Candidates should have strong experience in pharmaceutical or biotechnology CQV, a solid understanding of utility systems and validation principles, and excellent communication and documentation skills.