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Technical Writer Editor
Technical Writer EditorRose International • Newton, MA, USA
Technical Writer Editor

Technical Writer Editor

Rose International • Newton, MA, USA
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We are seeking a Technical Writer to join our Endovascular Robotics business within Advanced Therapies. This role involves translating complex technical engineering processes and details into clear, accurate, and compliant documentation for a cutting-edge medical robotics system. We are a global technology leader in robotic-assisted vascular interventions. We believe the combination of endovascular robotics, image guidance, and dedicated devices will change the way neurovascular procedures are done in the future, enabling better outcomes and enabling our customers to provide better access to care.

Required Education :

  • Bachelor’s degree in engineering, Technical Communication, Life Sciences, or related field

Required Experience / Skills :

  • 5+ years of experience in technical writing, preferably in medical devices or regulated industries
  • Strong attention to detail, organization, and ability to manage multiple projects
  • Excellent written and verbal communication skills

    • As a Technical Writer, you will be responsible for :

  • Author and revise IFUs, operator manuals, installation manuals, service manuals, and quick reference guides in accordance with FDA, MDR, and ISO standards
  • Translate complex engineering concepts into clear, concise, and accessible documentation for clinical and technical audiences
  • Collaborate with cross-functional teams (engineering, regulatory, human factors, QA) to gather source material and verify / validate content
  • Maintain version control and traceability of documentation
  • Support risk management and design history file (DHF) documentation as needed
  • Assist in developing templates, style guides, and documentation standards
  • This position may suit you best if you are familiar with what is below, and would like to develop your career with the client :
  • Familiarity with usability testing, risk management, and regulatory documentation (FDA 21 CFR Part 820, ISO 13485)
  • Experience with authoring tools (e.g., Adobe FrameMaker, MadCap Flare, Microsoft Word) and content management systems
  • Experience authoring IFU / operator manuals for highly complex medical devices
  • Only those lawfully authorized to work in the designated country associated with the position will be considered.
  • Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.
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    Technical Writer • Newton, MA, USA

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