A Global leading Medical Device Manufacturer based in Ireland is looking for a Human Factors Validation Engineer to join their dynamic team to support an ongoing product development project. This is a multi-year project which offers the opportunity to work on a life-saving device used for cancer treatments. This project offers vast professional development opportunities as you will be collaborating with teams of experienced engineers from different disciplines.
This is an exciting opportunity with candidates to start as soon as possible!
The Human Factors Validation Engineer must have a minimum of 3-5 years Human Factors and medical device experience as we need an individual who can work independently as well as part of a team. Day-to-day responsibilities include:

Design validation of the company’s medical device products, ensuring that these products meet user needs.
Leading (or participating in) human factors and design validation activities on complex medical devices over their complete lifecycle.

Experience Required:

Medical device system verification experience.
Experience on medical system design validation.
In-depth understanding of ISO13485, ISO62366, ISO14971, and FDA guidance on human factors and risk management.
Demonstrated expertise in one or more of the following validation specialties: clinical evaluation, end user validation, usability studies, or clinical trials.

If you are interested, please apply!
Job Title: Human Factors Engineer
Location: Blanchardstown, Ireland
Job Type: Contract
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