Quality Validation Engineer – Global Travel & Impact

Abbott Laboratories; Ireland; Remote; EUR 70,000 - 100,000; Full time

Benefits offered by this job

Family health insurance

Excellent pension scheme

Life assurance

Career Development

Fantastic new facility

Growing business

Job summary

Abbott Laboratories in Ireland, Kilkenny, is seeking a Quality Validation Engineer to create and maintain validation documentation for equipment, processes, and systems used in manufacture, control, and storage of products, ensuring compliance with Abbott Quality System requirements.

You will work with Quality, Engineering, Manufacturing and Operations to develop protocols, reviews, and validation plans, and support audits while driving risk assessments and validation activities across the site.

Qualifications

• Bachelor's Degree in Engineering, Science, Manufacturing, Quality, or a related discipline.
• 4+ years' experience in Engineering, Manufacturing, Scientific, or Quality environment.
• 5+ years' experience in validation including process, equipment, facilities, utility, and/or software validation.

Responsibilities

• Develop, review, execute, and maintain validation documentation (protocols, reports, risk assessments, validation plans).
• Ensure validation activities comply with procedures, regulatory requirements, and industry best practices.
• Support internal, customer, and regulatory audits as required.
• Track and communicate validation metrics and risks; drive continuous improvement.

Skills

Validation expertise

Quality systems

Regulatory compliance

Cross-functional collaboration

Documentation skills

Problem solving

Communication skills

Education

Bachelor's Degree in Engineering/Science/Manufacturing/Quality

Job description

Abbott Laboratories in Ireland, Kilkenny, is seeking a Quality Validation Engineer to create and maintain validation documentation for equipment, processes, and systems used in manufacture, control, and storage of products, ensuring compliance with Abbott Quality System requirements.

You will work with Quality, Engineering, Manufacturing and Operations to develop protocols, reviews, and validation plans, and support audits while driving risk assessments and validation activities across the site.