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QA Validation Engineer

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Onsite

QA Validation Engineer

CAI

QA Validation Engineer

Skills

Testing & QACompliance

2 months ago

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Important information


Contract type:

Permanent

Location:

Limerick, Ireland

Work mode:

Onsite

Published on:

2 September 2026

What they need


Are you a Validation Engineer looking to work on cutting-edge pharmaceutical and biotech projects in Ireland?

CAI is seeking a QA Validation Engineer to support qualification and validation activities for laboratory and process equipment across leading pharmaceutical and biotechnology facilities. This role offers the opportunity to work with a diverse range of analytical, manufacturing, and GMP-regulated systems while contributing to some of Ireland's most advanced life sciences operations.

Key Responsibilities

  • Execute IQ, OQ, and PQ activities for GMP equipment and systems.
  • Prepare and review validation protocols, reports, and lifecycle documentation.
  • Support commissioning, qualification, and validation projects from planning through execution.
  • Perform risk assessments and support deviation, CAPA, and change control activities.
  • Ensure compliance with GMP, GDP, and regulatory requirements.
  • Collaborate with Quality, Engineering, Manufacturing, and Laboratory teams.
  • Participate in audits and inspection readiness activities.
  • Support equipment lifecycle management and continuous improvement initiatives.

Requirements

  • Degree in Engineering, Science, Biotechnology, or a related discipline.
  • 3+ years' validation experience within pharmaceutical, biotechnology, medical device, or life sciences environments.
  • Experience qualifying laboratory and/or manufacturing equipment in GMP-regulated facilities.
  • Strong understanding of GMP and validation principles.
  • Experience authoring and executing validation documentation.
  • Knowledge of deviation management, change control, and CAPA processes.
  • Excellent communication and stakeholder management skills.
  • Strong technical writing and problem-solving abilities.
  • Eligible to work in Ireland.

Why Join CAI?

  • Work with leading pharmaceutical and biotechnology companies across Ireland.
  • Exposure to a wide range of validation and CQV projects.
  • Career development within a growing global organisation.
  • Collaborative and supportive team environment.
  • Competitive salary and benefits package.

About CAI CAI is a global leader in commissioning, qualification, validation, and operational readiness services for the pharmaceutical, biotechnology, and life sciences industries. We partner with leading manufacturers to deliver compliant, efficient, and innovative solutions that ensure quality and regulatory excellence.

Interested? Apply today and become part of a team delivering quality and compliance excellence across Ireland's world-leading life sciences industry.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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