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    • Drive software safety activities throughout the product lifecycle.
    • Strong understanding of software risk management and functional safety principles.
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    • Contributing to the development and maintenance of software solutions.
    • Supporting software integration, release, and maintenance activities.
    • Integrating embedded software with hardware systems ensuring seamless system performance.
    • Have strong expertise in embedded software (C/C++), system integration…
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    • Ensure all solutions adhere to Nuffield Health’s enterprise architecture and software engineering standards, with clear end‑to‑end design across platforms.
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    • You will be a key part in a community of world-class software engineers who will continuously improve, collaborate and innovate with other engineers to create…
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    • Validation Engineers in this space work to ensure Class III medical devices meet rigorous quality standards and regulatory requirements.
    • Carefully maintaining software design and code quality, enabling easier software updates and feature upgrades as the range becomes established.
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    • Working knowledge of ISO 13485 (medical device quality management) and IEC 62304 (medical device software lifecycle).
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    • System Validation Engineers in medical device settings could play a critical role in ensuring that Class III devices meet rigorous regulatory standards before…
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    • Conducting functional, performance and safety testing across hardware, software and integrated systems.
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    • Minimum of 3 years’ experience in testing hardware or electromechanical products (software testing experience is a plus, not essential).
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Medical Software Safety Engineer
Computer Futures
·
3.8
London
£75,000 a year
Permanent
Apply on company site

Job details

Here’s how the job details align with your profile.

Pay

£75,000 a year

Job type

Permanent

Full job description

We're partnering with an innovative medical technology consultancy looking for a Software Safety Engineer to support high-quality software-based medical devices. Key Responsibilities
  • Drive software safety activities throughout the product lifecycle.
  • Conduct hazard analysis, risk assessments, and safety documentation.
  • Collaborate with cross-functional teams including Software, Quality, Regulatory, and Product Development.
  • Ensure compliance with relevant medical device standards and regulatory requirements.
  • Support verification, validation, and software risk management activities.
Requirements
  • 4 years of experience within the medical device and/or Software as a Medical Device (SaMD) sector.
  • Strong understanding of software risk management and functional safety principles.
  • Knowledge of standards such as ISO 14971, IEC 62304, and related medical device regulations.
What's on Offer
  • Up to £85,000
  • Share option scheme
  • Potential hybrid flexibility
To find out more about Computer Futures please visit www.computerfutures.com Computer Futures, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC387148 England and Wales
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