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Validation Engineer EU Not Disclosed
Quality Engineer EU Not Disclosed
Senior Regulatory Affairs Specialist EU Not Disclosed
Senior Regulatory Affairs Specialist EU Not Disclosed
Senior Regulatory Affairs Specialist EU Not Disclosed
QA Engineer EU Not Disclosed
Quality Technician EU Not Disclosed
Quality Technician EU Not Disclosed
Senior Regulatory Affairs Specialist EU Not Disclosed
Senior Quality Engineer Galway Not Disclosed
Senior Quality Engineer Dublin Not Disclosed
Quality Manager EU Not Disclosed
Senior Quality Engineer EU Not Disclosed
Quality Systems Manager EU Not Disclosed
Senior Quality Engineer EU Not Disclosed
Senior Regulatory Affairs Specialist Dublin Not Disclosed

QA RA Engineer Career Profile


QA / RA Specialist

A role combining Quality Assurance and Regulatory Affairs, more often found in the Medical Device sector
Main Responsibilities
  • Apply technical solutions to problem solving
  • Apply technical solutions to quality improvement projects
  • Use technical writing skills to clearly describe technical information
  • Analyze customer complaints, identify trends and execute corrective actions
  • Understand standards and their application to medical devices
  • Planning, protocol generation, testing and report generation for medical devices
  • Generation and maintenance of technical files for medical devices
  • Review and update technical files in line with EU medical devices regulatory requirements
  • The use of harmonised standards when compiling a technical file in compliance with the MDD
  • Ensuring that records are filed in accordance with site procedures
  • Supporting R&D

Skills / Experience
  • Engineering / Science qualification
  • 3/4 years experience within R&D / QA/ RA/ Compliance or Validation function in a Medical Device Environment
  • Excellent technical writing experience within a medical device environment
  • 2/3 years experience in Risk, Clinical and Biocompatibility an advantage
  • Fluency in English

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