Manufacturing Engineer – Galway

If you have experience working in a regulated medical device environment with a focus on meeting quality service and cost objectives then this is the job for you!


  • Support key business metrics.
  • Reporting on yield, OEE metrics and product failure investigation.
  • Introduction of new products and process technology through process development and validation.
  • Use lean methodologies to drive continuous improvement.
  • Ensure that continuous improvement projects are completed.
  • Preparation and maintenance of manufacturing specifications for specific projects.
  • Ensure effective closure on quality system documents (Audit Actions, NC’s, CAPA’s, etc).
  • Ensure all production equipment, processes and work areas meet Health & Safety requirements.
  • Support all customer, FDA and NSAI audits.
  • Performing other tasks as required.


  • 4+ years’ experience in a medical device manufacturing environment.
  • BSc. in an engineering or technological discipline.
  • Ability to manage multiple assignments or projects.
  • Excellent analytical, troubleshooting and problem solving skills.
  • Knowledge of equipment and process validation.
  • Understanding of ISO 13485 and FDA design and development processes.
  • Work as part of a multi-disciplinary team.
  • Excellent planning and coordination skills and capable of initiating and leading change.
  • Must be authorised to work in Ireland.

Please contact Emer Moore to discuss in confidence


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