Senior Regulatory Specialist with experience in the medical devices sector required for permanent role with medical devices multinational in Offaly.


  • Third level qualification in an engineering or science discipline.
  • 5+ years’ experience in a Regulaory affairs role within the medical devices sector
  • Knowledge of EU Medical Device Directive, 21CFR820, 803 and 807, and ISO 13485 requirements.
  • Experience in internal auditing for compliance to Medical Device QSRs is an advantage.
  • Good planning and organizational abilities.
  • Ability to communicate effectively with management and peers.
  • Ability to work under own initiative, and strong team player.
  • Wiliness to travel to other sites.
  • Must be authorised to work in Ireland.

Please contact Emer Moore to discuss in confidence


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