Cpl are currently looking for a Human Factors Engineer to join a global leader in pharmaceutical innovation, supporting within their Drug Delivery Device team.
This is a 12m contract position (PAYE) based in Cambridge, hybrid working with an average of 2.5 days per week on site.
Key Responsibilities
- Lead and support Human Factors Engineering activities for drug delivery system projects.
- Coordinate with internal teams, external design partners, and human factors vendors to ensure timely execution of deliverables.
- Oversee project management related to the supply, assembly, and testing of materials for use in human factors studies.
- Provide usability input into device design and incorporate feedback into study findings and mitigation strategies.
- Manage and document use-related risk for assigned projects.
- Support the creation and maintenance of Instructions for Use (IFU) documentation.
- Assist in compiling human factors documentation for regulatory submissions.
- Offer guidance and expertise on human factors across internal teams.
Skills & Experience Required
- Experience in Human Factors Engineering, ideally within medical devices or combination products.
- Strong written English skills and the ability to write clearly for regulatory audiences.
- Excellent attention to detail and ability to prioritise tasks under pressure.
- Proficient in Microsoft Office (particularly PowerPoint); PC literate.
- Ability to work independently and collaboratively across multidisciplinary teams