Research and Development Engineer

Limerick
5 months ago
Applications closed

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Research & Development Engineer (Vascular)

We are actively seeking to recruit a Research and Development Engineer to become a key member of the R&D Team within a leading Limerick based Medical Device multinational.

This is an excellent opportunity to advance your career within a fast paced dynamic environment.

Responsibilities:

  • Design development, prototyping, test method design, design evaluation, design reviews, design specifications, design verification and validation, design protocols and reports, transfer to production activities in a timely effective manner.

  • Product testing and evaluation, completion of test reports to support design selection.

  • Preparation and presentation of design reviews.

  • Product and project risk analysis and risk management.

  • Development of the Design History File

  • Work with Process Development Engineering to introduce/develop new equipment and production processes as required for any new manufacturing techniques.

  • Source new materials components and equipment.

  • Development of component specifications, inspection methods, bills of materials and manufacturing processes.

  • Introduction of new equipment, materials and technologies.

  • Work closely with Key Opinion Leaders (KOL’s), physicians and product managers to develop innovative medical devices to improve patient care.

  • Project lead for assigned research & development projects including technical and project management responsibly.

    Qualifications and Experience:

  • Third level degree in Mechanical, Biomedical, Science, Design or similar discipline.

  • 3+ years’ design experience in medical device roles.

  • Third level degree in Mechanical, Biomedical, Science, Design or similar discipline.

  • Project planning skills.

  • Execution of project in a timely effective manner.

  • Knowledge of anatomy and physiology.

  • Good mechanical design and understanding of engineering fundamentals with extensive medical device materials knowledge.

  • Manufacturing design and process understanding.

  • Good working knowledge of Solidworks and/or Pro Engineer CAD.

  • Strong technical writer.

  • Knowledge of medical device quality & regulatory systems and medical device directives (ISO13485 and FDA CFR 820), EU Medical Device Regulation 2017/745.

  • Team Player with ability to develop strong working relationships.

  • Strong communication and inter-personal skills.

  • Good problem solving skills.

  • Highly motivated individual, self-starter with a passion for excellence.

  • Must be able to work in a fast paced environment.

  • Willingness and availability to travel on company business.

    For more information please forward your CV in the strictest confidence to (email address removed)

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