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Assoc MDR/Vigilance Specialist

Job description

Assoc MDR/Vigilance Specialist

Responsibilities:

  • Part of a team responsible for the management of all incoming product events from a range of sources and geographies
  • Responsible for the data entry of field complaints reported for medical devices into complaint database, including documentation review and complaint assessment
  • Support Vigilance and Medical Device Report (MDR) regulatory reporting by ensuring timely assessment of incoming complaint events
  • Support complaint trend analysis and issuance of key reports to relevant departments
  • Contribute to continuous improvement activities to support efficiency and productivity gains opportunities within the department
  • Build product knowledge and technical expertise of the product group you support
  • Adherence to procedures at all times to ensure compliance
  • Ensure highest quality of product event data entry for accuracy of reporting to regulatory agencies. Ensures complete and accurate maintenance and reporting of Medical Device, 0 years of experience required.

To apply for this position please contact Chloe Walsh at Sigmar Recruitment T: +353 91 455305 E:   chloe.walsh@sigmar.ie  

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