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Associate Quality Engineer

Location: Dublin
Experience:1-2 Years
Job Type:Permanent
Salary:Not Disclosed
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Associate Quality Engineer

Our client a high potential startup medical device company is currently seeking an Associate Quality Engineer to join their team. Reporting to the Quality Assurance Manager the associate Quality Engineer should have a hands-on approach to projects with a motivated attitude and strong work ethic. An ability to work in a flexible and small entrepreneurial environment is essential. The candidate will work on maintaining the Quality Management System. This a great opportunity for someone with 1-2 years’ experience looking to take next step in their career. Would also consider strong graduate with a relevant work placement


  • Support the QA Manager in development of quality plans, programs and procedures, through all aspects of the product development process.
  • Ensure all work is carried out in compliance with Quality, Regulatory and company policies and systems.
  • Ensure that performance and product quality conforms to company, customer and regulatory requirements.
  • Assists in the review, analysis and reporting on quality discrepancies related to product design and manufacture.

  • Coordinates, implements, and maintains the company’s Document Control and Training System.
  • Coordinates labelling activities through change management interfacing with suppliers to meet quality standards and timelines.
  • Strictly follows established procedures and policies needed to meet the demands of document control in a regulated medical device company.
  • Assists in supporting external audits.
  • Maintains quality records per applicable SOPs.
  • Investigates and responds to corrective actions related to Document Control.
  • Responsible for coordinating document change notifications (DCN) approvals and release.
  • Supports incoming inspection activities.
  • Maintains records in clinical trial folders.


  • Bachelor’s degree in a relevant Engineering or Science field
  • 0-2 years’ experience in the medical device industry or other regulated industry

  • Strong verbal, written, organizational, time management and interpersonal skills
  • Strong computer skills, including working knowledge of MS Office and e-mail


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