We are working with a medical devices R&D company, based in Limerick, that is seeking a R&D/Design Engineer with 3–5 years’ experience in medical device development. This role will focus on supporting new product design activities, ensuring high‑quality documentation, and enabling compliance with regulatory standards.Key ResponsibilitiesSupport new medical device design and development activities in line with regulatory and quality requirementsGenerate, review, and approve Design History File (DHF) documentation.Participate in design reviews and cross‑functional collaboration with R&D, Quality, and Manufacturing teams.Ensure compliance with ISO 13485, FDA, and EU MDR requirements for design control.Requirements2–5+ years’ experience in medical device designStrong knowledge of medical device development processes and quality systems.Experience with SEMS (Self-Expanding Metal Stents) is preferred; however, other delivery systems will be accepted.Degree in Biomedical or Mechanical Engineering.This is an initial 12-month contract role, with a view to an extension or potential to become permanent.€45-58/hour DOE3 days onsite per week is required.If you are interested, please apply using the links provided. Please note that sponsorship is not provided for this position.
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