Associate R&D Engineer- Medical Device Start-Up

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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