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Research & Development Engineer II

ID
14382
Location
Limerick, Ireland
Role Type
Permanent
Contact
Johanne Kennedy
Email
choices@hero.ie
Phone
+353 86 440 3725
LinkedIn
click here
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  • 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/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.
  • Compliance with Quality, Regulatory and company policies and systems.
  • Communications: o Regular communication to cross-functional teams, senior management and business unit leaders. o Project status communications and reporting.
  • Bachelor’s degree in Engineering or a related field is required.
  • Minimum of 3 years’ relevant experience is required
  • Demonstrated project planning skills ans execution of project in a timely effective manner.
  • 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.
  • Willingness and availability to travel on company business.

Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval.

For further information on this please contact Johanne Kennedy on 0864403725 / choices@hero.ie Check out all our open jobs on our HERO Recruitment website – https://www.hero.ie/

Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval Data can only be transferred outside of the EEA on the basis of standards contractual clauses, to a country for whom an adequacy decision has been given by the European Commission or where the express permission of the data subject has been given. You have supplied us with your personal data in the process of applying for a position. Our client company may have personnel outside of the EEA who will review your data. We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.

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