Quality Engineer

Job description

Quality Engineer

The Quality Engineer will work as part of the Quality and Regulatory Affairs teams and be responsible for tasks supporting the Companys’ Operations function.  


  • Develop and implement inspection procedures for incoming components, in process assemblies and final product and manage and co-ordinate all inspection activities.
  • Manage and implement procedures for non-conforming product.
  • maintain PFMEA and provide direction in the development of validation protocols and reports.
  • Review DHR records and prepare product release documentation.
  • Support the continuous improvement of quality system processes and the business generally.
  • Complete tasks as designated by your supervisor to support the needs of the business


  • Bachelor’s degree in Science or Engineering is a pre-requisite for this role.  
  • A minimum of 2 years’ experience in a quality engineering or regulatory role ideally in a regulated environment. Medical device industry experience is an advantage.
  • A self-starter who can see and deliver the work required to advance the company goals with a minimal amount of direction.
  • Excellent written, interpersonal communication and presentation skills.
  • Holds him/herself and others accountable to meet commitments by following through, acting with a clear sense of ownership, and taking personal responsibility for decisions, actions and failures.


To apply for this position please contact Keeva O’Shea at Sigmar Recruitment T: +353 91 749264 E:

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