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Principal Research & Development Engineer

ID
14634
Location
Galway, Ireland
Role Type
Permanent
Contact
Johanne Kennedy
Email
choices@hero.ie
Phone
+353 86 440 3725
LinkedIn
click here

Principal Research & Development Engineer

Similar Jobs
Principal R&D Engineer – Clinical Engineering Group
Location: Galway, Ireland

Our client, a global leader in medical devices, is seeking a Principal R&D Engineer to join their Clinical Engineering Group, working on the innovative ACURATE Transcatheter Aortic Valve device. This exciting opportunity is based at their state-of-the-art facility in Galway. The successful candidate will leverage their technical expertise and leadership skills to drive impactful projects, collaborate with leading physicians, and support cutting-edge innovations that make a real difference in patients' lives.

About Galway, Ireland: Located on the stunning west coast of Ireland, Galway offers a vibrant community, a rich cultural heritage, and a high quality of life, making it an ideal place to live, work, and thrive.

Key Responsibilities:

  • Physician-Facing Research: Lead and manage physician-facing research projects on ACURATE PRIME, partnering directly with physicians and field teams across the US and EMEA.
  • Technical Project Leadership: Drive technical projects and complex case support, including CT segmentation and 3D printing, to deliver breakthrough solutions.
  • Innovation & Engineering Excellence: Perform pioneering engineering work as part of major programmes, defining strategic technology impacts that align with long-term site goals.
  • Subject Matter Expertise: Act as a recognised expert in your field, influencing site-wide technology planning and innovation.
  • Mentorship & Team Development: Mentor and coach technical staff, providing structured training to enhance skills and productivity.
  • Product Performance Insight: Demonstrate a thorough understanding of how manufacturing impacts product performance, delivering value to customers.
  • Environmental Impact Assessment: Collaborate with EHS teams to evaluate new equipment, processes, and chemicals, ensuring minimal environmental impact.

Quality System Commitment:

  • Demonstrate a commitment to patient safety and product quality by adhering to the company’s Quality Policy and procedures.
  • Ensure resources are in place to maintain compliance with the Quality System and uphold the organisation’s high standards.
  • Foster a work environment that supports the Quality Policy and drives continuous improvement.

Education & Experience:

  • Degree: Level 8 Bachelor’s Degree (240 credits) in Engineering or Science, preferably Mechanical, Materials, or Biomedical Engineering.
  • Experience: Minimum of 5+ years in a design, manufacturing, or healthcare environment, with hands- on R&D/technical experience in the medical device sector highly desirable.
  • Technical Skills: Proven experience in design, fixture development, and customer-facing roles.
  • Interpersonal Skills: Strong communication, analytical, and problem-solving abilities.
  • Travel: Willingness to travel up to 25%.

 

Join an innovative team making a global impact and be part of a company that values your expertise and commitment to excellence. Apply now to take the next step in your career with a world-leading medical device company in Galway, Ireland.

For more information on this role in please contact Johanne Kennedy on +353 86 440 3725 / 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 you data. We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.








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