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Salary
$95k – $106k per year
Location
In office (Amsterdam, Dublin)
Visa
No sponsorship (stated in the posting)
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 12, 2026. First seen by Alion on Sep 7, 2026. CAI scores D on the Alion truth index.

Overview
Company
Impact
Profile match

CAI

CAI is a professional services firm headquartered in Indianapolis, Indiana, providing commissioning, qualification and validation, operational readiness and staff augmentation services to the life sciences and mission critical industries, including pharmaceutical plants and data centers. Established in 1996, it has grown to nearly 800 people working on client projects in North America, Europe, Asia and Australia. It hires commissioning project managers and engineers for data centers, CQV and computer system validation engineers, automation and sterility assurance engineers, quality and regulatory specialists and global finance directors.
Backed by JLL Partners

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.

Why CAI?

At CAI, our people are at the heart of everything we do. We partner with the world's leading life sciences companies to deliver innovative projects that ultimately improve patient lives. You'll work alongside industry leading experts in a collaborative environment that supports professional growth and technical excellence.

If you're a CQV professional looking to contribute to a challenging pharmaceutical project while developing your career with a global consultancy, we'd love to hear from you.

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