Location: Arden Hills, MN
Duration: 12+ months


You will work collaboratively with development teams to create customer-facing manuals and labels necessary to support the client’s worldwide regulatory, marketing, and sales objectives. By joining their Technical Communications team, your work will be a part of the life-saving products used around the world.


  • Plan, analyze, and create content using technical writing theories, methods, and tools
  • Assist with administrative authoring tasks, including routing documents for approvals, and reviewing documents for accuracy and conformance to standards
  • Interpret and apply corporate processes to ensure compliance with regulatory and standard-based requirements
  • Ensure document content quality by managing and organizing information for accuracy, consistency, and readability
  • Establish and manage content across different documents and product types in a manner that promotes consistency and efficiency
  • Identify, analyze, recommend, and implement innovative solutions to drive continuous improvement in technical writing processes and practices


  • Bachelor’s degree plus 2-5 years of related experience
  • Experience technical writing in the medical device or other regulated industry
  • Strong collaboration skills
  • Ability to work in a fast-paced environment
  • Demonstrated ability to handle multiple tasks and projects
  • Attention to detail
  • Ability to adapt and innovate in a changing environment


  • Experience with a content management system
  • Experience with InDesign and Adobe Creative Suite 6
  • Ability to operate within complex processes
  • Experience in technical writing used for translated documentation

Click to submit a resume or find additional support.