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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.
    • The role ensures that controlled documents, quality records and agreed quality-system workflows are maintained accurately, progressed in a timely manner and…
    • Experience defining performance and quality indicators, analyzing monitoring trends, and translating insights into recommendations for senior leadership.
    • Strong knowledge of quality management systems and applicable regulatory expectations.
    • Experience working with digital tools for quality management, analytics…
    • A broad quality role offering the opportunity to develop further experience across QMS, auditing, CAPA, complaints and regulatory compliance within a medical…
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    • Experience in the regulated medical device industry, ideally supporting product lifecycle and regulatory compliance activities.
    • This role is a UK based role and any hybrid/remote work must also be within the UK.
    • This is a hands-on, field-based role where no two days are the same.
    • Support the Site Quality Manager with budgeting, monitoring and controlling medical QC expenditure.
    • Manage shift analysts, the analytical support chemists and…
    • Significant QA leadership in clinical quality, PV quality or both, including leading global teams in a complex matrix; experience across both GCP and GVP is…
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    • Access to professional development in medical device regulation and compliance standards.
    • Regulatory Specialists play a central role in ensuring that medical…
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    • Proven experience in medical device sales, ideally within surgical or theatre-based environments.
    • Deliver high-quality product demonstrations, clinical support…
    • Previous experience working within a quality-driven environment, ideally within the medical device, pharmaceutical, healthcare or other regulated industry.
    • Experience within a manufacturing, medical devices or similar operational environment.
    • Identifying and delivering process improvements that enhance efficiency…
    • Experience within pharmaceutical, medical device or another regulated manufacturing environment would be advantageous.
    • Night Shift - (4 on, 4 off).
    • The Production Engineer plays a key role in supporting the successful introduction and manufacture of Bedfont’s medical devices.
    • Well-being garden and room.

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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