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    • This permanent role will see you play a key part in assessing and improving Quality Management Systems for software-based medical devices.
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    • Working knowledge of ISO 13485 (medical device quality management) and IEC 62304 (medical device software lifecycle).
    • Ensure compliance with relevant medical device standards and regulatory requirements.
    • Knowledge of standards such as ISO 14971, IEC 62304, and related medical…
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    • Professional development in regulated medical device environments.
    • Domain: Class III medical device · validation and regulatory compliance.
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    • Domain: Class III medical device · system validation.
    • Professional development in medical device compliance and validation methodologies.
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    • Experience in the regulated medical device industry, ideally supporting product lifecycle and regulatory compliance activities.
    • The Production Engineer plays a key role in supporting the successful introduction and manufacture of Bedfont’s medical devices.
    • Well-being garden and room.
    • A background in regulated medical devices.
    • This role is for an engineer who enjoys the full journey of a product: designing the electronics, building and…
    • This is a specialist hands-on role where your technical expertise, judgement, and problem-solving skills will be central to delivering high-quality, bespoke…
    • Experience contributing to electrical and electronic hardware designs, from requirements through to integration and verification.
    • As a Design Assurance Engineer, you will play a pivotal role in enabling our transition from research-focused product delivery to medical-device grade design…
    • Working within the Engineering support Team and reporting to the Controls System Lead Engineer, the Software/Controls Engineer (SCE) is responsible for…
    • Knowledge of regulated or safety-critical sectors (automotive, medical devices, aerospace and defence, industrial and rail).
    • Benefits: Private medical, 2x pension contribution, lease car scheme, cycle to work scheme, 25 days holiday (plus public holidays) and more.
    • Electrical and electronic diagnostic skills.
    • Carry out maintenance and system breakdowns on medical and life science systems completing reports on time in…

Job Post Details

Medical Device Auditor
Computer Futures
·
3.8
London
£75,000 a year
Permanent
Apply on company site

Job details

£75,000 a year
Cycle to work scheme
Permanent
London

Full job description

Medical Device Auditor - London / Remote We are partnering with our client to help them appoint a Medical Device Auditor. This permanent role will see you play a key part in assessing and improving Quality Management Systems for software-based medical devices. Key Skills & Experience
  • Medical Device Industry Experience (4+ years)
  • ISO 13485 QMS Auditing/Management
  • EU MDR / UK MDR for QMS
  • Software & SaMD Expertise desirable
Offered:
  • Up to £90,000 per annum
  • Share options
  • EV and cycle to work scheme
Interested? If you are looking to apply your quality expertise in a high-impact role within our client's team, please apply to this with your CV and we'll be in touch! 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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