CQV Engineer

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

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.
• Experience Required
• Previous CQV experience within pharmaceutical, biotech, or life sciences manufacturing environments.
• Strong understanding of commissioning and qualification methodologies.
• Experience supporting regulated manufacturing facilities and associated utility systems.
• Exposure to complex process equipment and containment-focused manufacturing operations is highly desirable.
• Familiarity with GMP documentation, protocol execution, and project lifecycle delivery.
• Preferred Experience
• Candidates with experience in one or more of the following areas are particularly encouraged to apply:
• High containment or high potency manufacturing environments
• Process equipment qualification
• Manufacturing support systems and clean utilities
• HVAC and facility qualification
• Packaging, processing, or solid dosage manufacturing operations
• Safety critical or hazardous processing environments
• Other Requirements
• This is a site-based role
• Eligible to work in the EU without the need for visa sponsorship, now or in the future.