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R&D Engineer II

ID
15107
Location
Limerick
Role Type
Contract
Contact
Emma Griffin
Email
quality@hero.ie
Phone
+353 860334325
LinkedIn
click here

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R&D Engineer II

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Research And Development Engineer

Job Title: R&D Engineer – Aortic Vascular Innovation Program

Location: Limerick (Hybrid)

Type: Contract

Department: Research & Development

About the Role

We are seeking a highly motivated and driven R&D Engineer to join our dynamic team supporting a pioneering R&D project within the Aortic Vascular program. This is a unique opportunity to play a key role in the design and development of an innovative endovascular repair device aimed at treating complex aortic aneurysms and dissections.

You will contribute to the full lifecycle of a cutting-edge medical device—from initial concept and feasibility through to design, verification, validation, and eventual commercialisation. Your work will help bring forward a novel solution to address significant unmet patient needs in the treatment of life-threatening aortic conditions.

Key Responsibilities

  • Contribute to the design, development, and refinement of a next-generation aortic endovascular repair system.
  • Support feasibility studies, prototype development, and functional testing.
  • Assist in defining and executing verification and validation plans, ensuring compliance with regulatory requirements (e.g., ISO 13485, FDA 21 CFR Part 820).
  • Collaborate closely with cross-functional teams including clinical, regulatory, quality, and manufacturing.
  • Participate in risk management activities, including FMEA and design hazard analysis.
  • Document design controls in line with internal and external standards.
  • Engage in iterative design processes using input from clinical experts, pre-clinical testing, and simulation data.
  • Contribute to the preparation of technical documentation for regulatory submissions and design reviews.
  • Stay abreast of emerging trends in endovascular technologies and aortic repair therapies.

Qualifications and Skills

  • Bachelor’s or Master’s degree in Biomedical Engineering, Mechanical Engineering, or a related field.
  • 1–5 years of experience in medical device design and development (preferably within cardiovascular or endovascular domains).
  • Hands-on experience with CAD tools (e.g., SolidWorks) and rapid prototyping techniques.
  • Understanding of anatomy and physiology relevant to vascular/aortic systems is a strong plus.
  • Strong analytical and problem-solving skills with a creative, innovation-driven mindset.
  • Excellent communication and teamwork abilities.
  • Experience working in a regulated environment (e.g., ISO, FDA) desirable.
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