QA Validation Engineer – GMP CQV (Ireland)

Cagents; Limerick; On-site; EUR 60,000 - 90,000; Full time

Benefits offered by this job

Competitive salary

Benefits package

Job summary

CAI is seeking a QA Validation Engineer to support qualification and validation activities for laboratory and process equipment across pharmaceutical facilities in Ireland. You will work on IQ/OQ/PQ for GMP systems and prepare lifecycle documentation while ensuring regulatory compliance.

Join a diverse team and contribute to audits, CAPA, and continuous improvement initiatives while collaborating with Quality, Engineering, Manufacturing, and Laboratory groups.

Qualifications

• Degree in Engineering, Science, Biotechnology, or related discipline.
• 3+ years' validation experience in pharma/biotech/life sciences environments.
• Experience qualifying laboratory and/or manufacturing equipment in GMP 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.
• 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

Communication skills

Stakeholder management

Technical writing

Problem solving

GMP & validation principles

Education

Bachelor's degree in Engineering/Science

Job description

CAI is seeking a QA Validation Engineer to support qualification and validation activities for laboratory and process equipment across pharmaceutical facilities in Ireland. You will work on IQ/OQ/PQ for GMP systems and prepare lifecycle documentation while ensuring regulatory compliance.

Join a diverse team and contribute to audits, CAPA, and continuous improvement initiatives while collaborating with Quality, Engineering, Manufacturing, and Laboratory groups.