Document Controller – Medical Devices – with experience in a QA function in an FDA or ISO 13485 regulated environment required for permanent role with medical devices multinational in Offaly. The successful candiate will manage documentation associated with medical devices & new product transfers. 


  • Documentation management, including processing, distribution and filing of all documents
  • Initiation of change requests for new and amended documents
  • Routing of controlled documents through the approval and implementation process
  • Issue and maintenance of controlled documentation
  • Reporting on document control metrics as required



  • 2+ years experience within a QA function in an FDA or ISO 13485 regulated industry
  • Understanding of data accuracy, document control and the importance of attention to detail.
  • Ability to communicate effectively with management and fellow peers.
  • Experience with Oracle; Agile and Access advantageous.
  • Must be authorised to work in Ireland.

Please contact Emer Moore to discuss in confidence

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