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Assoc MDR Vigilance Specialist | Hybrid

  • Sector: Engineering
  • Contact Email:
  • Job Ref: 20553

Our client a major multinational here in Galway are looking to hire an Associate MDR & Vigilance Specialist on an initial 23 month contract.


  • Monitors the company's drug or medical devices surveillance program including the intake, protocol development, evaluation, processing, and follow-up on adverse reports, participation in the resolution of any legal liability and in complying with government regulations.
  • Ensures complete and accurate maintenance and reporting of Medical Device Reports (MDRs), Adverse Drug Experience (ADE) data or adverse reaction data as required by regulatory agencies.
  • Review and analyze clinical databases for the extraction of ADE data and integrates the data to ensure the creation of a unified database consistent with the aims and purposes of ADE standardization and internalization as well as to ensure the accuracy and quality of safety summaries.
  • Acts as a liaison internally and with external collaborators to develop programs and processes to meet regulatory reporting requirements.


  • Qualified person to Bachelor’s degree (Level 8 NFQ) in Engineering/Science or related discipline.
  • 2 years relevant experience 
  • Dynamic team player, attention to detail, goal-orientated, good communicator and problem solving skill-sets.
  • Medical device experience desirable
  • 100% desk based

For more information or a confidential discussion about this role please contact Michelle Mc Inerney

091 706 717