Quality Assurance Engineer

Abbott Ireland Vascular Division

On-sitePosted 4 августа 2026 г.

About the role

Quality Assurance Engineer

Abbott Ireland Vascular Division

On-sitePosted 4 августа 2026 г.

About the role

Abbott Ireland Vascular Division is seeking a Quality Assurance Engineer, Intermediate, based in Clonmel, Ireland. Abbott Vascular focuses on advancing vascular disease treatment through device innovations, pharmaceutical products, and ongoing R&D and training. This role sits at the intersection of manufacturing, quality, and product development and is designed for someone who helps ensure high-quality, compliant products while driving continuous improvement across manufacturing operations.

Responsibilities

Drive Quality & Compliance: identify and resolve manufacturing issues (scrap, non-conformances, and customer complaints) using structured root cause analysis; implement robust CAPA.
CAPA & Audit Activity: lead CAPA processes, prepare and respond to audits, and maintain inspection readiness.
Regulatory & ISO Compliance: review processes and documentation to ensure alignment with ISO and regulatory standards; embed compliance in daily activities.
New Product Introductions (NPI): collaborate with cross-functional teams on launches to ensure quality from development to commercialization.
Major Projects: participate in compliance initiatives, process optimization, and project rollouts.
Continuous Improvement: lead or contribute to CIP initiatives using data-driven approaches, Lean principles, and Six Sigma to reduce variation and improve performance.
Data-Driven Process Optimization: use monitoring systems to identify critical control points and enhance process capability.
Product & Process Development: contribute to quality plans, risk assessments, and FMEA

Responsibilities

Drive Quality & Compliance: identify and resolve manufacturing issues (scrap, non-conformances, and customer complaints) using structured root cause analysis; implement robust CAPA.
CAPA & Audit Activity: lead CAPA processes, prepare and respond to audits, and maintain inspection readiness.
Regulatory & ISO Compliance: review processes and documentation to ensure alignment with ISO and regulatory standards; embed compliance in daily activities.
New Product Introductions (NPI): collaborate with cross-functional teams on launches to ensure quality from development to commercialization.
Major Projects: participate in compliance initiatives, process optimization, and project rollouts.
Continuous Improvement: lead or contribute to CIP initiatives using data-driven approaches, Lean principles, and Six Sigma to reduce variation and improve performance.
Data-Driven Process Optimization: use monitoring systems to identify critical control points and enhance process capability.
Product & Process Development: contribute to quality plans, risk assessments, and FMEA

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