Contract Human Factors Engineer - Medical Devices Usability

SoCode Limited

Stockholms kommun

Hybrid

SEK 585,000 - 975,000

Full time

3 days ago
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Job summary

SoCode Limited is seeking an experienced Contract Human Factors Engineer in Cambridge on a hybrid basis for a 3-month assignment. The role focuses on usability studies for advanced medical devices, including moderation, observation, data analysis, and reporting.

You’ll work with an established team following FDA-aligned quality procedures, with fieldwork required and eligibility to work in the UK. Up to £400 per day on a contract basis.

Qualifications

  • Proven, hands-on human factors experience on medical devices.
  • Experience running usability study sessions as moderator or observer.
  • Strong data analysis skills to turn session feedback into clear findings and practical recommendations.
  • Experience planning studies and writing protocols and reports to a high, regulation-ready standard.
  • Good working knowledge of FDA expectations for human factors work.
  • Excellent communication and attention to detail, with the confidence to join an established team quickly.
  • Availability for a full week or more of fieldwork, including preparation and dry runs.
  • Eligibility to work in the UK.

Responsibilities

  • Involved in the full study cycle, from planning and running sessions as moderator or observer, through analysing data and writing actionable reports.
  • Out in the field with real users for formative study, with recruitment/venues managed by others.
  • Work closely with a colleague on the study, following established quality procedures aligned with FDA guidance.

Skills

Human factors engineering
Usability studies
Data analysis
Study planning
FDA expectations

Job description

SoCode Limited is seeking an experienced Contract Human Factors Engineer in Cambridge on a hybrid basis for a 3-month assignment. The role focuses on usability studies for advanced medical devices, including moderation, observation, data analysis, and reporting.

You’ll work with an established team following FDA-aligned quality procedures, with fieldwork required and eligibility to work in the UK. Up to £400 per day on a contract basis.

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