Overview
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
1. Lead and support Human Factors Engineering activities for drug delivery system projects.
2. Coordinate with internal teams, external design partners, and human factors vendors to ensure timely execution of deliverables.
3. Oversee project management related to the supply, assembly, and testing of materials for use in human factors studies.
4. Provide usability input into device design and incorporate feedback into study findings and mitigation strategies.
5. Manage and document use-related risk for assigned projects.
6. Support the creation and maintenance of Instructions for Use (IFU) documentation.
7. Assist in compiling human factors documentation for regulatory submissions.
8. Offer guidance and expertise on human factors across internal teams.
Skills & Experience Required
9. Experience in Human Factors Engineering, ideally within medical devices or combination products.
10. Strong written English skills and the ability to write clearly for regulatory audiences.
11. Excellent attention to detail and ability to prioritise tasks under pressure.
12. Proficient in Microsoft Office (particularly PowerPoint); PC literate.
13. Ability to work independently and collaboratively across multidisciplinary teams
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