Job Summary:
This role is ideal for an experienced Human Factors Engineer looking to contribute to the design and delivery of innovative medical devices.
* Lead human factors processes for novel medical device design, ensuring compliance with EU and FDA regulations
* Coordinate user studies and develop project plans to meet performance, time, and cost targets
* Develop and deliver design and risk management documentation for human factors
* Act as voice of the customer in product and user experience design
* Support preparation of compliance package for product evaluation/certification
* Lead clinical studies involving developed products
* Ensure full compliance with quality, regulatory, health, and safety legislation
* Maintain design development traceability and control changes
Requirements:
* Strong background in human factors engineering and medical device design
* Proven experience in leading human factors processes and coordinating user studies
* Excellent communication and project management skills
* Ability to work effectively in a team environment