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Quality Specialist II

Role Type
Mark Wilson
+353 86 0449473
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Quality Specialist II
County Clare

The Quality Specialist for Immunoassay/Blood Virus is responsible for the generation, investigation and implementation of actions arising from Non-conformances, complaints and deviations within the department, as well as the maintenance of operator training records.  The Quality Specialist also reviews batch history records and completes change controls and supports continuous improvement efforts.

You will be a part of the IA/BV Production Operations team reporting to the Production Supervisor and will be responsible for quality investigations, procedural updates, BHR compliance as well as support of audit preparations and continuous improvements. If you thrive in a multifunctional, fast paced, supporting role and want to work to build a world-class production organization.

In this role, you will have the opportunity to:

  • Investigate and close non conformances, deviations, change controls, and other quality system controls
  • Support department in audit proceedings and preparations
  • Final Batch History Record review for compliance
  • Training of production operators on procedural and documentation updates
  • Maintenance of training records for department
  • Support and Implement continuous improvements
  • Support coordinators in Line Clearance

Education & Experience

  • Bachelor’s Degree in Science or Engineering with 2+ years’ experience or Master’s degree in relevant field
  • Experience in Quality Systems
  • Valid work permit or right to work in Ireland

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

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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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