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Technical Writer

Full-Time England, United Kingdom
Health & Biotech
Health & Biotech
19 August 2025
Description
  • Drives creation and updates of technical documentation and label generation using defined processes.
  • Responsible for the upload and maintenance of documents on the eIFU platform in conjunction with the Product Management team
  • Work collaboratively with stakeholders to ensure inputs and outputs align and where necessary, actively participate in VPM, attend project core teams and provide accurate, timely updates on status and escalating actions to drive to resolution.

The essential requirements of the job include:

  • Demonstrates problem solving; analyses possible solutions using standard process and use knowledges and experience to drive a resolution.
  • Sound judgement with ability to balance business and customer needs, with a sense of urgency.
  • Strong Project Management skills, effectively manages several document/label updates simultaneously without support and provides accurate and clear updates on work and timeframes. Capable of managing and adjusting to changing priorities and competing deadlines.
  • Explains complex information to others in straightforward situations.
Qualifications
  • Degree or equivalent experience, desirable
  • Content Management System experience, desirable
  • Experience within the Medical Device industry or other regulated industries.

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