QA Validation Engineer

CAI; Dublin; On-site; EUR 70,000 - 90,000; Full time

Job summary

CAI is seeking a QA Validation Engineer in Ireland to support qualification and validation activities for laboratory and process equipment across GMP facilities. You will execute IQ, OQ, and PQ, prepare validation protocols and reports, and contribute to lifecycle documentation while collaborating with Quality, Engineering, Manufacturing, and Laboratory teams.

The role offers exposure to analytical, manufacturing systems and CQV projects, with emphasis on risk assessments, deviation handling,

Qualifications

• Degree in Engineering, Science, Biotechnology, or a related discipline.
• 3+ years' validation experience within pharmaceutical/biotech/Life sciences.
• Experience qualifying laboratory and/or manufacturing equipment in GMP facilities.
• Strong understanding of GMP and validation principles.
• Experience authoring and executing validation documents.
• Knowledge of deviation management, change control, and CAPA processes.
• Excellent communication and stakeholder management skills.
• Eligible to work in Ireland.

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.

Skills

QA validation

GMP understanding

Communication

Technical writing

Stakeholder management

Problem-solving

Education

Engineering/Science/Biotechnology degree

Job description

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.

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.