Human Factors Engineer
Location: Cambridge, UK
Reports to: Human Factors Team
About the Role
A Human Factors Engineer position is available within a leading Drug Delivery Devices Centre of Excellence based in Cambridge, UK. This team supports the design and development of innovative drug delivery systems, working across multiple therapy areas to ensure that devices are safe, effective, and intuitive to use.
The role focuses on the execution of human factors engineering (HFE) activities, from early design input through to regulatory documentation, helping ensure products meet both user needs and regulatory expectations.
Key Responsibilities
Collaborate with internal project teams, external design partners, and human factors vendors to plan and deliver HFE activities.
Manage the supply, assembly, and testing of materials for use in human factors studies.
Provide usability and design feedback, incorporating study outcomes into design improvements.
Identify, assess, and document use-related risks for assigned projects.
Support the development and control of Instructions for Use (IFU) and related documentation.
Contribute to the preparation of human factors reports for regulatory submissions.
Offer expert guidance on human factors processes and best practices.
Essential Skills and Experience
Minimum 3 years’ experience in Human Factors Engineering, ideally in medical devices or combination products.
Proven experience conducting usability studies and managing use-related risk assessments.
Excellent written communication skills, with the ability to produce clear, concise technical documentation.
Strong attention to detail and ability to work under pressure to meet deadlines.
Effective project and time management abilities.
Proficient in Microsoft Office applications (Word, PowerPoint, Excel, Outlook).
Capable of working independently or collaboratively within multidisciplinary teams.
Desirable Qualifications
Advanced qualification in Human Factors, Usability Engineering, or a related discipline.
Understanding of regulatory requirements for medical devices and combination products.
Background in a medical, scientific, or engineering field.