R&D Engineer

• Contract Role
• Hybrid
• Limerick
• Medical Device
  
  The R&D Engineer position in Limerick involves working under the Senior R&D Engineer or R&D Manager. The role entails design development, prototyping, testing, evaluation, risk management, and collaboration with cross-functional teams. The engineer will lead assigned R&D projects, ensuring timely completion of milestones, and contribute to innovation through patent filings. Regular communication with cross-functional teams, senior management, and business unit leaders is essential.

Qualifications / Requirements:

• A third level degree in a related discipline 4 years of medical device design experience
• Experience in DHF documentation for medical devices (DFMEAs, protocols, reports, DIVTs)
• Class III medical device design experience (stent & delivery systems, thrombectomy or atherectomy devices)
• Design documentation skills
• Project planning skills CAD knowledge (Solidworks and/or Pro Engineer)
• Strong problem-solving abilities
• Good communication and interpersonal skills
• Ability to work in a fast-paced environment
• Willingness and availability to travel on company business
• Knowledge of medical device quality & regulatory systems and medical device directives (ISO13485 and FDA CFR 820), EU Medical Device Regulation 2017/745.

Additional information: It's important to find a company that aligns with your career aspirations and values. Take the time to find the right opportunity for you.

For further information on this role in Limerick please contact Emma Griffin on quality@hero.ie or 086 0334325

Check out all our open jobs on our HERO Recruitment website – https://www.hero.ie/

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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 you data. We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.