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Senior R&D Engineer

Job Posted: 21 hours ago

  • Salary: £ Competitive

    Job Type: Permanent

  • Location: Limerick, Limerick County

Expire in: a month

Job Description

Senior Research & Development Engineer (Vascular) An opening for a Senior R&D Engineer has arisen within a leading Munster based Medical Device multinational. This is an excellent opportunity to develop your career within a dynamic and progressive 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 and effective manner. * Product and project risk analysis and risk management. * Develop prototypes which are consistent with the clinical and design requirements of the project. * Research new therapies and design solutions to develop and complement the existing product portfolio. * Introduce 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 team/s including technical and project management leadership responsibly. * Mentoring, coaching and development of direct reports if required. * Regular communication to cross-functional teams, senior management and business unit leaders. Qualifications and Experience * Third level degree in Mechanical, Biomedical, Science, Design or similar discipline, Masters or Ph.D. level preferred but not essential. * 5+ years’ experience is ideal. * Proven Project Leadership abilities. * Good Project Management methodology and skills. * Proven track record in delivering quality results in a timely effective manner. * Knowledge of anatomy and physiology. * Good mechanical design and understanding of engineering fundamentals with extensive medical device materials knowledge. * Innovative/Creative Engineer. * Good manufacturing design and process understanding. * Good working knowledge of Solidworks and/or Pro Engineer CAD. * Good presentation skills (working knowledge of MS PowerPoint). * Strong technical writer. * Attention to detail and Quality focus. * Good working knowledge of medical device quality & regulatory systems and medical device directives (ISO13485 and FDA CFR 820). * Experience of medical device development from concept through to commercialisation. * Ability to effectively translate needs of clinicians and SBU into project inputs. * Willingness and availability to travel on company business

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