Quality Engineer I (Medtech)

TL;DR

Quality Engineer I (Medtech): Supporting new product development teams by maintaining quality standards and protocols with an accent on regulatory compliance and process precision. Focus on conducting non-conformance investigations, implementing testing procedures, and ensuring documentation meets reliability standards within a medical device manufacturing environment.

Location: Hybrid role based in Galway, Ireland

Salary: €41,600 – €62,400

Company

A global leader in healthcare technology dedicated to alleviating pain, restoring health, and extending life through innovative engineering solutions.

What you will do

• Develop and maintain quality standards and protocols for new products during development phases.
• Collaborate with R&D, engineering, and manufacturing teams to ensure quality compliance.
• Devise methods for inspecting, testing, and evaluating product precision and accuracy.
• Perform non-conformance investigations and implement corrective measures.
• Support internal and external audit preparation and documentation maintenance.
• Contribute to continuous improvement activities to support business performance goals.

Requirements

• Bachelor’s degree (Level 7 NFQ) in Engineering, Science, or a related discipline.
• Minimum of 1 year of relevant experience in a medical device environment.
• Practical knowledge of statistical data analysis and quality improvement tools.
• Strong technical writing and organizational skills.
• Ability to multi-task and take initiative in a fast-paced environment.

Culture & Benefits

• Competitive salary and flexible benefits package.
• Eligibility for the hirify.global Incentive Plan (MIP).
• Opportunity to work on life-saving medical technology.
• Commitment to diversity, equity, and inclusion.
• Supportive environment focused on career growth and professional development.