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Quality Technician II - Evenings

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Quality Technician II – Evenings

Are you passionate about ensuring top-notch quality in the medical device industry? We are seeking a dedicated Quality Technician to join our clients team. In this role, you will make crucial product dispositions, update documentation, and conduct thorough inspections throughout the production process. Your responsibilities will include managing Engineering Change Orders, performing First Article Inspections, resolving Non-Conformance Reports, and participating in continuous improvement initiatives like Kaizen events.


  • Make product dispositions as and when required.  Update documentation such as specifications and visual standards to better define the quality characteristic being dispositioned.  
  • Prepare and update documentation such as Work Instructions, Product Routings (CHR’s), Visual Standards etc. as required.
  • Prepare Engineering Change Orders (ECO’s). Obtain the necessary approvals and where necessary implement on the document control system.
  • Perform inspections on product (incoming, in-process and final) as required.  This may arise due to product quality investigations, incoming inspection capacity etc.
  • Prepare process data such as yield, output rates, No. of NCR’s etc.
  • Perform First Article Inspections as required.
  • Raise Non-Conformance Reports and ensure associated product is segregated, oversee that NCR’s are closed out in a timely manner.
  • Oversee the execution of validation activity as required. 
  • Carry out scheduled audits (Internal, Standard Work, out of the box etc.)
  • Participate in improvement activities, including Kaizen events.
  • Adhere to Plant Safety requirements and Health & Safety requirements relating to your work, assuming responsibility for those aspects of the OH&S System over which you have control to ensure the health and safety of yourself and others.
  • Be aware of the potential environmental impacts associated with your work and the implications of non-conformance.
  • Contribute to enhanced energy performance by conservation of energy where possible (Lighting, Equipment, Air Conditioning etc).
  • Contribute to the continual improvement activities of the OH&S, Environmental and Energy Management systems through participation, providing feedback/ suggestions for improvement and by reporting accidents, dangerous occurrence, near miss/ illness, good catch and environmental incidents in a timely manner.
  • To take on other duties which the Company may assign you from time to time. These ‘other duties’ will be agreed with Management prior to any assignment.


  • Diploma qualification Quality or a related discipline Or significant relevant experience in a quality assurance role within the Medical Device Industry. 
  • A minimum of 3 years’ experience in a similar Quality related role in the Medical Device / Components industry.


For further information on this role in Shannon, Clare please contact Katie Kilbane on +353 86 1283368 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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