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QA Validation Engineer

CagentsLimerick, IE

EngineeringFull time
Source-verified: read directly from this employer's own lever job board, not a repost.On-sitePosted (3 months ago)Last verified (today)

At a glance

Location
Limerick, IE
Workplace
On-site
Pay
Not published by the employer
Employment type
Full time
Experience
Not stated
Education
No degree requirement stated
Job family
Engineering
Seniority
Not stated
Posted by employer
23 July 2026
Last verified open
23 October 2026
Region and country
IE
Team
Europe Life Sciences
Listed via
Lever

What the employer wrote

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.

Where this record came from

Read from Cagents's own Lever job board on , and last confirmed still open on . The employer published it on 23 July 2026. Jobsearch.ing did not write, edit or rank this posting, and does not vet the employer. View the original posting.

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