C
C AgentsQA Validation Engineer
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Before you apply
LocationLimerick
Work modeon-site
Typefull-time
SeniorityMid
Experience3+ yrs
DepartmentEurope Life Sciences, North Europe
Company size501–1,000 people
PostedJul 23, 2026 · 3mo ago
Verified live1d ago
May no longer be actively hiring
Posted by the company on Jul 23, 202677% of this company's open roles have been listed for 90+ days
At a glanceSummarised by Seekless from the posting.
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
Skills
CAPA
change control
deviation management
GMP
GDP
IQ
OQ
PQ
About the role
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
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Execute IQ, OQ, and PQ activities for GMP equipment and systems.
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Prepare and review validation protocols, reports, and lifecycle documentation.
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Support commissioning, qualification, and validation projects from planning through execution.
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Perform risk assessments and support deviation, CAPA, and change control activities.
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Ensure compliance with GMP, GDP, and regulatory requirements.
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Collaborate with Quality, Engineering, Manufacturing, and Laboratory teams.
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Participate in audits and inspection readiness activities.
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Support equipment lifecycle management and continuous improvement initiatives.
Requirements
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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?
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Work with leading pharmaceutical and biotechnology companies across Ireland.
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Exposure to a wide range of validation and CQV projects.
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Career development within a growing global organisation.
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Collaborative and supportive team environment.
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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.