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Salary
≈ $48k – $103k per year (Estimated)
Location
In office (Limerick)
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 25, 2026. First seen by Alion on Jul 20, 2026. CAI scores C 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

Are you an experienced CQV Engineer looking to join a dynamic project team delivering complex pharmaceutical or life sciences projects?

We are seeking a driven and collaborative CQV professional to support commissioning, qualification and validation activities across a range of GMP regulated systems, facilities and equipment. This is an excellent opportunity to work on high impact projects in a fast paced and technically challenging environment.

Key Responsibilities

  • Execute Commissioning, Qualification and Validation (CQV) activities in line with project schedules and GMP requirements.
  • Support commissioning, startup and qualification of equipment, utilities and process systems.
  • Prepare, review and execute validation documentation including protocols, reports, and traceability matrices.
  • Lead or participate in design reviews, FATs, SATs, commissioning, IQ, OQ and PQ activities.
  • Manage qualification documentation through the full CQV lifecycle.
  • Coordinate activities with engineering, operations, quality, contractors and equipment vendors.
  • Track progress, identify risks and support timely project delivery.
  • Assist with change controls, deviations, punch lists and documentation management.
  • Ensure all activities are performed to the highest safety and compliance standards.
  • Provide technical support during project execution and system handover

What We're Looking For

  • Experience within Pharmaceutical, Biotechnology, Medical Device or Life Sciences industries.
  • Background in Commissioning, Qualification, Validation, Engineering or Technical Operations.
  • Understanding of GMP and regulated manufacturing environments.
  • Experience working with equipment, process systems, clean utilities, facilities or automation systems.
  • Strong documentation, problem-solving and stakeholder engagement skills.

    Ability to work effectively as part of a multidisciplinary project team.

Why Apply?

  • Opportunity to work on industry-leading projects
  • Exposure to cutting-edge manufacturing technologies
  • Collaborative and supportive team environment
  • Competitive salary or contract rates available
  • Potential for long-term career progression

Interested in learning more? Apply today!

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