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BSI

Global standards and business improvement partner

Technical Specialist - Active Medical Devices

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-time£58.5k - £78k /yr

About the Job

Requirements

  • Four years of professional experience in healthcare products or related activities, such as manufacturing, auditing, or research, including two years in the design, manufacture, testing, or use of the device or technology to be assessed, or related scientific aspects.
  • A bachelor’s degree or higher in a discipline relevant to the medical device industry, which may include electronic/electrical, electro-mechanical, or biomedical engineering, or medical physics.
  • Familiarity with the Medical Devices Regulation (EU) 2017/745 and/or Medical Devices Directive 96/42/EEC is an advantage.
  • At minimum, awareness of the requirements of the IEC 60601 family of standards and ISO 14971 risk management standard.
  • Understanding of design control and risk management principles.
  • Strong interpersonal communication skills.
  • Ability to prioritize and execute an individual workload.
  • Professional experience gained in accredited testing laboratories and broad exposure to a range of active medical devices are noted as successful-role backgrounds.

Responsibilities

  • Review and evaluate medical device technical and clinical documentation in areas of competence to assess compliance with MDD 93/42/EEC, MDR 2017/745, and UK MDR 2012 schemes.
  • Manage certification activities for a portfolio of medical device manufacturers, including determining auditing requirements and making recommendations for issuing and maintaining CE certifications.
  • Provide specialist regulatory, operational, and strategic support to medical device scheme managers, product specialists, and the business in delivering CE medical device marking schemes.
  • Provide medical device expertise, leadership, and mentoring in areas of competence to medical device personnel.

Desired Qualifications

  • Familiarity with the Medical Devices Regulation (EU) 2017/745 and/or Medical Devices Directive 96/42/EEC.
  • Professional experience gained in accredited testing laboratories and broad exposure to a range of active medical devices.

About the Company

BSI

Global standards and business improvement partner

BSI is a global standards and business-improvement partner that helps organizations grow by addressing society’s critical issues, from climate change to trustworthy AI. It works by developing and applying standards, certifications, training, assessment, and assurance services that enable clients to manage risk, improve governance, and demonstrate compliance. Its products operate through a worldwide network of experts, industry groups, and governments, delivering audits, certifications, and advisory guidance to help clients meet specified requirements and improve performance. What sets BSI apart is its scale and breadth: a 100-year history, a global community of 15,000 experts and 77,500+ clients across many sectors, and a collaborative approach with regulators, industry bodies, and stakeholders to implement standards in real-world operations. The company’s goal is to help clients fulfil theirs by creating trust and accelerating progress toward a fair society and a sustainable world.

Company size
5,001-10,000
Company stage
Not listed
Total funding
Not listed
Headquarters
London, United Kingdom
Founded
1901

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