CQV Engineer — GMP Pharma Validation & Commissioning

CAI; Netherlands; On-site; EUR 65,000 - 95,000; Full time

Job summary

CAI is seeking experienced Commissioning, Qualification & Validation (CQV) Engineers to support a large scale pharmaceutical manufacturing project. This role offers the opportunity to work within a multidisciplinary team delivering critical process, utility, and facility qualification activities in a GMP regulated environment.

Execute CQV activities, develop qualification documentation, support system turnover, and coordinate with engineering, quality, operations and project stakeholders to

Qualifications

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

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

GMP knowledge

Pharma manufacturing

Cross-functional teamwork

Education

Bachelor's degree in Engineering

CQV certification

Tools

Qualification documentation

Job description

CAI is seeking experienced Commissioning, Qualification & Validation (CQV) Engineers to support a large scale pharmaceutical manufacturing project. This role offers the opportunity to work within a multidisciplinary team delivering critical process, utility, and facility qualification activities in a GMP regulated environment.

Execute CQV activities, develop qualification documentation, support system turnover, and coordinate with engineering, quality, operations and project stakeholders to