Technical Writer
CMR Surgical
Cambridge, UK
1d ago

We’re looking for a keen, curious and extremely detail-orientated technical writer to support the production of high-quality design documentation.

Working within the Technology Division, you will utilise your attention to detail and ability to assimilate technical information to help develop and maintain design and hazard analysis documentation.


You’ll be part of a multi-skilled dynamic team, and your main responsibilities will be :

  • Creating and editing documents for internal and external audiences
  • Collaborating with the design teams to maintain up-to-date documentation in line with standards for medical device development including the risk analysis
  • Researching, digesting, clarifying and presenting technical information, in text and diagrams
  • Supporting the development of summative protocols and reports
  • Supporting senior engineers in developing the necessary paperwork to support regulatory filings
  • Reviewing external documents for consistency, accuracy, and adherence to internal requirements
  • We’re a high growth company and as such roles change and evolve.We’d expect you to be willing to turn your hand to anything within the Technology Division remit that helps it to deliver its objectives.

    About You

    Naturally you’ll be enthusiastic about writing and making documents clear, functional and accurate. You will have a 2 : 1 (or equivalent) in a relevant technical degree.

    You’ll enjoy finding things out by talking to colleagues from different disciplines, and you will be curious, energetic and proactive, and a great team player.

    You will ideally have some or all of the following :

  • Excellent verbal and written presentation skills
  • An analytical approach and a quick grasp of functions and relationships of parts across a complex system
  • Attention to detail and consistency across a large number of documents
  • An ability to portray information effectively using graphics and photos
  • Experience with Microsoft Word, ideally editing macros, templates and styles
  • A track record of creating high quality technical content, perhaps in writing up research projects
  • Experience within a technical medical device environment
  • Experience of using Requirement Management Tools
  • An understanding of risk documentation (FMEA)
  • An ability to understand and cross-reference regulatory standards documents
  • The Package

    We offer a competitive salary and a great benefits package. In addition, you’ll be joining a company with a fabulous culture of ambition, creativity and teamwork, and where fun is just as valued as our commitment to make surgery better for millions of people.

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