CQV Engineer (GMP, Pharma) — EU Site

CAI; Dublin; On-site; EUR 65,000 - 90,000; Full time

Job summary

CAI seeks experienced CQV Engineers to support a large-scale pharmaceutical manufacturing project in the Netherlands. The role delivers commissioning, qualification, and validation activities for processes, utilities, and facilities within a GMP environment.

You will develop and execute qualification documentation, coordinate with engineering, quality, operations, and project teams, and support turnover, startup, and operational readiness.

Qualifications

• Previous CQV experience within pharmaceutical, biotech, or life sciences manufacturing environments.
• Strong understanding of commissioning and qualification methodologies.
• Experience supporting regulated manufacturing facilities and utility systems.
• Familiarity with GMP documentation, protocol execution, and project lifecycle delivery.

Responsibilities

• Execute commissioning and qualification activities for process, utility, and facility systems.
• Develop, review, and execute qualification documentation in line with project and regulatory requirements.
• Support system turnover, startup, and operational readiness activities.
• Liaise with engineering, quality, operations, and project stakeholders to ensure successful project delivery.
• Participate in walkdowns, punch-list resolution, and troubleshooting activities.
• Ensure compliance with site quality, safety, and GMP procedures.

Skills

CQV experience

Pharma industry

GMP documentation

Job description

CAI seeks experienced CQV Engineers to support a large-scale pharmaceutical manufacturing project in the Netherlands. The role delivers commissioning, qualification, and validation activities for processes, utilities, and facilities within a GMP environment.

You will develop and execute qualification documentation, coordinate with engineering, quality, operations, and project teams, and support turnover, startup, and operational readiness.