Quality Engineer – Galway

An excellent opportunity to join a leading medical device organisation based in Galway.

Key Responsibilities:

  • Partner with R&D and Process Engineers to ensure that the transition of products.
  • Promotes compliance and excellence within the company.
  • Participates in new product/technology development.
  • Executes the project design plans, protocols and generates reports for new product development projects. 
  • Defines and implements Quality standards and specifications.
  • Develops and executes required validations in line with regulatory standards.
  • Conducts root cause analysis and implements corrective action.
  • Conducts audits, including closing out audit findings.
  • Creates and maintains company quality documentation.



  • BSc. in Engineering or Quality Assurance Degree.
  • 3+ years experience as a Quality Assurance Engineer within a Medical Device or regulated environment.
  • Demonstrable detailed working knowledge of the medical device industry.
  • A good team player, who works well in a small team environment.
  • A good communicator who can easily convey ideas.
  • Capacity to make sound judgements while learning from mistakes.
  • Detailed knowledge of the regulatory environment in which the business operates.
  • Attention to detail while maintaining awareness of longer-term objectives.
  • Capacity to maintain the highest levels of confidentiality internally and externally.
  • Ability to stay connected to multiple projects simultaneously.
  • Must be authorised to work in Ireland.


Please contact Emer Moore to discuss in confidence

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