Pharma CQV Engineer — GMP, Onsite in Europe

Cagents

Amsterdam

On-site

EUR 70,000 - 110,000

Full time

7 days ago
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Job summary

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

Join a dynamic project team and contribute to successful turnover, startup, and operational readiness in a regulated setting with exposure to

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 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.

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.

Job description

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

Join a dynamic project team and contribute to successful turnover, startup, and operational readiness in a regulated setting with exposure to

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