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Quality Engineer

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Mark Wilson
+353 86 0449473
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Recruitment Consultant

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Quality Engineer

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Quality Engineer

HERO Recruitment are proud to be partnered with an Irish owned leading medical device company in Limerick who are a key partner of the world’s largest orthopedic manufacturers.

Our Client provides manufacturing solutions and design services while leveraging the latest technologies and equipment to create the highest quality of devices. This is an exciting opportunity for an experienced Quality Technician or a Quality Engineer who wants a role in a company where there work has a positive impact on patient’s live globally.

Key Responsibilities:

  • Investigate manufacturing product quality and compliance issues (e.g., CAPA, non-conformances, audit observations) for all production processes prior to final product release based on engineering principles; analyze results, make recommendations and develop reports.
  • Collaborate with operations manager to develop and implement controls and improvements.
  • May develop, update, and maintain technical content of risk management files.
  • Develop training and documentation materials for production (e.g., work instructions) to enable the seamless knowledge transfer of project and manufacturing processes.
  • Assign support tasks; gives instruction to technicians on supporting projects; trains technicians and provides feedback; and may coordinate technician work.
  • Investigates any Customer Complaints.
  • Participates in internal audit and supplier audit programs for relevant ISO’s such as ISO 13485 and ISO14001.
  • Lead defect resolution, root cause investigation, and continuous improvement activities.
  • Support FMEA and Inspection development to ensure that all failure modes in process have been identified and addressed.
  • Coordinate quality data and reporting of KPIs to drive continuous improvement and feed into management review.
  • Project activities as required from NPI projects.
  • Lead site change control activities.
  • Other incidental duties assigned by management.
  • Lead and develop quality administrator.

Key Requirements:

  • Minimum degree in a science, quality, engineering or related discipline.
  • Minimum 2 years industry experience.
  • Strong written and oral communication skills.
  • Experience working with medical device regulations.

For further information on this role in please contact Mark Wilson on 0860449473 or email

Check out all our open jobs on our HERO Recruitment website –

Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval.

Data can only be transferred outside of the EEA on the basis of standards contractual clauses, to a country for whom an adequacy decision has been given by the European Commission or where the express permission of the data subject has been given. You have supplied us with your personal data in the process of applying for a position. Our client company may have personnel outside of the EEA who will review you data. We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.



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