Quality Engineer I: Impact, Compliance & Innovation

Medtronic plc; Galway; Hybrid; EUR 42,000 - 62,000; Full time

Benefits offered by this job

Flexible Benefits Package

Job summary

Medtronic plc in Ireland seeks a Quality Engineer to support manufacturing quality standards, collaborating with Engineering, Manufacturing and Quality teams to ensure regulatory compliance and patient safety. You will analyze quality data, participate in CAPAs, NCMRs, validations, and drive continuous improvement across the product value stream.

The role offers a competitive salary and flexible benefits in a dynamic medical device environment.

Qualifications

• Bachelor's degree in Engineering, Science or technical field.
• Analytical and problem-solving skills with risk-based approach.
• Ability to work in cross-functional teams; develop technical and quality knowledge.

Responsibilities

• Supports development, modification, application, and maintenance of quality standards and procedures for manufacturing processes and finished products.
• Collaborates with Engineering, Manufacturing and Quality teams to ensure compliance with quality systems.
• Participates in investigations, NCMRs, CAPAs, and validation activities under guidance.
• Assists in implementing and maintaining product control measures for quality and patient safety.
• Reviews quality data, identifies trends, and supports problem-solving.
• Supports inspection and testing activities and analyzes product/process performance.
• Ensures quality records are completed accurately and maintained per regulatory requirements.
• Contributes to continuous improvement initiatives to enhance quality and performance.

Skills

Analytical skills

Problem-solving

Cross-functional teamwork

Communication skills

Time management

English fluency

Education

Bachelor's degree in Engineering, Science or technical field

Tools

SAP

SAP ME

Job description

Medtronic plc in Ireland seeks a Quality Engineer to support manufacturing quality standards, collaborating with Engineering, Manufacturing and Quality teams to ensure regulatory compliance and patient safety. You will analyze quality data, participate in CAPAs, NCMRs, validations, and drive continuous improvement across the product value stream.

The role offers a competitive salary and flexible benefits in a dynamic medical device environment.