Human Factors Engineer

Position Summary

Join us as a Human Factors Engineer where you will help design easy-to-use and safe healthcare solutions. You will work closely with cross-functional teams to understand user needs and bring these insights into the design process. Our team values curiosity, empathy, and collaboration.

Responsibilities

• Lead human-centred design activities throughout all stages of device development to ensure products meet user needs.
• Plan and execute user studies, including early handling tests and design validation, to gather meaningful feedback.
• Conduct user-related risk assessments and integrate findings into design decisions to improve safety and usability.
• Work closely with engineers, regulatory, clinical, and quality teams to solve design and regulatory challenges.
• Manage relationships and communications with external vendors and internal stakeholders to support project goals.
• Contribute to regulatory documentation by preparing clear, accurate sections related to human factors and usability.

Basic Qualifications

• Degree in Mechanical Engineering, Biomedical Engineering, Human Factors, or a related field.
• Proven experience applying human factors engineering principles in medical device or combination product development.
• Understanding of human factors regulatory guidelines such as IEC 62366 and FDA usability requirements.
• Experience planning and conducting human factors studies, including usability testing and risk assessments.
• Knowledge of integrating user needs and risk information into design and validation activities.
• Strong communication skills to work effectively within cross-functional teams and with external partners.

Preferred Qualifications

• Experience with global regulatory submissions and authoring sections of human factors files.
• Ability to analyse user data and translate insights into clear design improvements.
• Familiarity with design for manufacture principles.
• Strong organisational skills with the ability to manage multiple projects and deadlines.
• Evidence of being a proactive team player who adapts well to changing priorities.
• High attention to detail and commitment to quality.

Working Arrangement

This role is based at GSK's Research & Development site in Ware, Hertfordshire, United Kingdom. We offer a flexible hybrid working arrangement with an expectation for regular on-site presence. Occasional travel may be required.