Cache of job #13898844

Job Title

R&D Engineer

Employer

Brightwater

Location

Limerick

Description

Are you a design focused engineer with experience of Medical Device R&D? An opportunity has arisen to join a high performing team at a leading employer in Limerick and work on a diverse range of projects. Responsibilities. Perform Duties of Research & Development Engineer: 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. Work with Process Development Engineering to introduce/develope 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. Compliance with Quality, Regulatory and company policies and systems. Educating oneself in the medical area for which the new devices are being developed in order to have an appreciation for what needs to be achieved with these products. Qualifications. Third level degree in Mechanical, Biomedical, Design, Chemical Engineering or similar discipline. 2 Years design experience medical device roles. Project planning skills. 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. For more on the role call Nigel on 021 4221000 or send your CV for consideration. This job originally appeared on RecruitIreland.com.

Date Added

2138 days ago

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