Quality Assurance Engineer (Intermediate) — Medical Devices

Abbott

Ireland

On-site

EUR 45,000 - 65,000

Full time

4 days ago
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Benefits offered by this job

Health benefits

Job summary

Abbott in Ireland is seeking a Process/Quality Engineer to support manufacturing and ensure the delivery of high-quality products. Based in Clonmel, you will contribute to quality plans, risk analyses and CAPA, working within a regulated quality environment to enable continuous improvement across the Vascular division.

You will apply quality tools, mentor junior staff, and participate in validation and discrepancy investigations to sustain Abbott's standards and patient safety.

Qualifications

  • NFQ Level 7 qualification (or equivalent).
  • 2+ years relevant experience in quality engineering.
  • Experience in a regulated quality environment (GMP/ISO).

Responsibilities

  • Identify manufacturing process defects and perform root cause analysis.
  • Support development of product quality plans, specifications, risk analyses and FMEA.
  • Use process monitoring systems to identify critical steps and reduce variation.
  • Assist product/process improvement efforts using quality metrics and analysis.
  • Apply and develop proficiency in quality tools and training materials.
  • Participate in validation activities (protocol/report writing, execution).
  • Support corrective and preventive actions (CAPA).
  • Participate in Field Discrepancy Notification (FDN) investigations.

Skills

Quality systems
Regulatory knowledge
Process improvement
Root cause analysis
Project coordination
Team mentoring

Education

NFQ Level 7

Tools

CAPA
FMEA

Job description

Abbott in Ireland is seeking a Process/Quality Engineer to support manufacturing and ensure the delivery of high-quality products. Based in Clonmel, you will contribute to quality plans, risk analyses and CAPA, working within a regulated quality environment to enable continuous improvement across the Vascular division.

You will apply quality tools, mentor junior staff, and participate in validation and discrepancy investigations to sustain Abbott's standards and patient safety.

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