Quality Validation Engineer - Medical Devices, Global Impact

Abbott; Kilkenny; On-site; EUR 70,000 - 95,000; Full time

Benefits offered by this job

Family health insurance

Excellent pension scheme

Life assurance

Career Development

New facility

Job summary

Abbott is seeking a Quality Validation Engineer at its Kilkenny site to create and maintain validation documentation for equipment, processes, facilities and systems used in manufacturing, control and storage of products. You will ensure compliance with Abbott Quality System and regulatory standards, and work with global teams across Europe and the United States.

Ideal candidates will have 5+ years in validation and a strong background in regulated industries such as Medical Devices or

Qualifications

• Bachelor's Degree in Engineering, Science, Manufacturing, Quality or related discipline.
• 4+ years in engineering, manufacturing, scientific or quality environments.

Responsibilities

• Develop, review, execute, and maintain validation documentation (protocols, reports, risk assessments, validation plans).
• Support site validation program development, implementation and continuous improvement.
• Ensure validation activities comply with divisional procedures, regulatory requirements and best practices.
• Develop and maintain Quality System procedures, work instructions and training materials.
• Monitor and maintain compliance status of validation and quality records.
• Collaborate with Quality, Engineering, Manufacturing and Operations to meet validation objectives.
• Support internal, customer and regulatory audits as required.
• Track validation metrics and risks, driving continuous improvement.

Skills

Problem-solving

Communication

Stakeholder management

Independent working

Education

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

Job description

Abbott is seeking a Quality Validation Engineer at its Kilkenny site to create and maintain validation documentation for equipment, processes, facilities and systems used in manufacturing, control and storage of products. You will ensure compliance with Abbott Quality System and regulatory standards, and work with global teams across Europe and the United States.

Ideal candidates will have 5+ years in validation and a strong background in regulated industries such as Medical Devices or