Associate R&D Engineer- Medical Device Start-up
Permanent
Galway
€30000 - €38000 per annum

Job Title: Associate R&D Engineer
Location: Galway
Job Type: Full-time | On-site
Industry: Medical Devices
About the Company
Our client is an innovative medical device start-up focused on developing next-generation solutions to address unmet clinical needs. Backed by strong technical leadership and a clear commercial vision, they are entering an exciting phase of product development and are looking to grow their R&D team.
Role Overview
We are seeking a motivated and high-achieving Associate R&D Engineer to join the team and contribute to the design, development, and testing of novel medical devices. This is a hands-on role ideally suited for a recent graduate with strong technical fundamentals, creativity, and a desire to grow within a fast-paced start-up environment.
Key Responsibilities
- Assist in the design and prototyping of medical devices using 3D CAD and rapid prototyping tools.
- Support the execution of feasibility and verification testing in accordance with design control procedures.
- Participate in the development of test methods, protocols, and reports.
- Maintain detailed documentation to support regulatory submissions and IP generation.
- Work closely with cross-functional teams including Quality, Regulatory, and Manufacturing to support product development milestones.
- Contribute to continuous improvement initiatives and provide input on materials, processes, and device performance.
Requirements
- A 1st Class Honours Degree in Biomedical Engineering, Mechanical Engineering, or a closely related discipline.
- Strong problem-solving skills and the ability to apply engineering fundamentals to complex challenges.
- Experience with SolidWorks or similar CAD software.
- Excellent communication skills, both written and verbal.
- A proactive, self-motivated attitude with the flexibility to adapt to the evolving needs of a start-up environment.
Desirable (but not essential)
- Internship or academic project experience in medical device design or testing.
- Familiarity with ISO 13485, FDA design controls, or cleanroom practices.
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This position was pPosted on 01 Jul 2025
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