Quality Engineer – Galway

Quality Projects Engineer required to join a growing Medical Device multinational based in Galway.

Key Responsibilities:

  • Support teams to achieve business objectives & performance in line goals and KPI’s.
  • Overall responsibility for production GMP standards and compliance.
  • Establishing inspection standards, plans, frequencies and test methods.
  • Preparing and updating operations procedures and associated documentation while maintaining compliance.
  • Maintain relevant documentation to comply with quality standards and customer requirements.
  • Development and executing Validation documentation which aligns with the receiving sites Quality system.
  • Develop strong links with customer and other project stakeholders.
  • Performing an active role in further development and continuous improvement of the quality management system.



  • BSc. in Quality or Science / Engineering.
  • 5+yrs industry experience in a medical device-manufacturing or pharmaceutical environment.
  • Experience within a similar role as quality engineer.
  • Working knowledge of FDA and ISO Quality systems.
  • New product introduction and manufacturing process transfer experience advantageous.
  • Experience in developing and executing Equipment and Process Validations.
  • Quality experience in component and device manufacturing advantageous.
  • Must be authorised to work in Ireland.

Please contact Emer Moore to discuss in confidence

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