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Human Factors Engineer - 35368-1

SRG
Posted 2 days ago, valid for 15 days
Location

Cambridge, Cambridgeshire CB21NT, England

Salary

£22.39 - £23.39 per hour

Contract type

Full Time

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Sonic Summary

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  • The position is for a Human Factors Engineer on a 12-month contract based in Cambridge.
  • The role offers a pay rate of £23.39 per hour (PAYE) or £26.21 per hour (Umbrella).
  • Candidates must have a minimum of 3 years of experience in Human Factors Engineering, specifically within the medical device or combination product sector.
  • Key responsibilities include leading usability studies, managing risk documentation, and advising on regulatory expectations.
  • The role supports hybrid working and requires strong written communication skills and proficiency in Microsoft Office tools.

Title: Human Factors Engineer
Length: 12-month contract
Rate: 23.39 per hour (PAYE) | 26.21 per hour (Umbrella)
Location: Cambridge

Our client is seeking a Contract Human Factors Engineer to support the development of drug delivery systems across multiple therapeutic areas. This full-time role offers a hybrid working arrangement and involves collaboration with internal teams, external design partners, and human factors vendors.
Key Responsibilities:

  • Lead and coordinate human factors engineering activities, including planning and executing usability studies and managing associated materials.
  • Provide expert input into device design processes, usability risk assessments, and mitigation strategies.
  • Develop and maintain use-related risk documentation and contribute to regulatory submissions.
  • Support the creation and revision of Instructions for Use (IFUs) for combination products.
  • Advise cross-functional teams on human factors best practices and regulatory expectations.

Essential Skills & Experience:

  • Minimum 3 years of experience in Human Factors Engineering; must have experience within the medical device/combination product space.
  • Strong written communication skills, particularly in drafting documentation for regulatory authorities.
  • Proven ability to manage multiple projects and meet deadlines under pressure.
  • Proficiency in Microsoft Office tools, especially PowerPoint.
  • Ability to work independently and collaboratively across teams.

Desirable Qualifications:

  • Advanced degree in Human Factors, Usability Engineering, or a related discipline.
  • Familiarity with regulatory frameworks for medical devices and combination products.
  • Background in healthcare, life sciences, or biomedical engineering.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

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