Quality Validation Engineer
Abbott · Kilkenny, Ireland
QualityFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Abbott seeks a Quality Validation Engineer for its Kilkenny diabetes care manufacturing facility. The role involves developing and maintaining validation documentation for equipment, processes, and systems while ensuring compliance with regulatory standards and quality procedures.
What they're looking for
- Bachelor's degree in Engineering, Science, Manufacturing, Quality, or related discipline
- Minimum 4 years experience in Engineering, Manufacturing, Scientific, or Quality environment
- 5+ years experience in validation (process, equipment, facilities, utility, software)
- Experience in regulated industries such as Medical Devices, Pharmaceuticals, or Biotechnology
- Strong knowledge of FDA 21 CFR Part 820 and ISO 13485 requirements
- Experience authoring and reviewing validation lifecycle documentation
- Understanding of risk management principles and validation best practices
What you'll be doing
- Develop, review, execute, and maintain validation documentation including protocols, reports, and plans
- Support development and continuous improvement of the site validation program
- Collaborate with Quality, Engineering, Manufacturing, and Operations teams on validation objectives
- Monitor compliance status of validation and quality records, tracking metrics and trends
- Support internal, customer, and regulatory audits as required
Privacy & handoff
This role links to Abbott's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.