Medical Device Technical Writer — IFU & Documentation

SNT Medtronic Navigation, Inc.

United States

On-site

USD 68,000 - 102,000

Full time

3 days ago
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Benefits offered by this job

Health, Dental and vision insurance
Life insurance
401(k) plan with employer match
Tuition assistance

Job summary

Medtronic CST in Lafayette, Colorado is seeking a technical writer to develop and maintain Instructions for Use and related product documentation for regulated medical devices throughout the product lifecycle. The role partners with Product Development, Marketing, and Regulatory Affairs to ensure accuracy, compliance, and global accessibility.

You will use Adobe FrameMaker and structured authoring tools, manage version control, coordinate translations, and mentor junior writers.

Qualifications

  • Bachelor's degree in a technical field or writing discipline with 2+ years of technical writing experience.
  • Experience creating documentation for regulated medical devices.
  • Advanced proficiency with Adobe FrameMaker.
  • Experience with Structured Authoring, XML, and CMS.

Responsibilities

  • Develop, update, and maintain IFU, manuals, and other product documentation.
  • Collaborate with cross-functional teams to gather content.
  • Create documentation using FrameMaker and structured authoring tools.
  • Manage version control and document release in PLM systems.
  • Coordinate multilingual translation projects.
  • Review, edit, and ensure clarity and compliance.
  • Support process improvements in documentation workflows.
  • Provide guidance and mentor junior writers.

Skills

Technical writing
FrameMaker
XML
Content management systems
Adobe Acrobat
Adobe Photoshop
HTML
Vector graphics

Education

Bachelor's degree in Technical Science / English / Journalism or related writing discipline

Tools

Vasont CMS
Structured authoring tools

Job description

Medtronic CST in Lafayette, Colorado is seeking a technical writer to develop and maintain Instructions for Use and related product documentation for regulated medical devices throughout the product lifecycle. The role partners with Product Development, Marketing, and Regulatory Affairs to ensure accuracy, compliance, and global accessibility.

You will use Adobe FrameMaker and structured authoring tools, manage version control, coordinate translations, and mentor junior writers.

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