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Technical Writer II

Employer
Horizontal Talent
Location
Saint Paul
Salary
Competitive

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Purpose Statement

You will work collaboratively with development teams to create customer-facing manuals and labels necessary to support our clients worldwide regulatory, marketing, and sales objectives.

Key Responsibilities
  • 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 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

Quality System Responsibilities

In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.

Required Qualifications
  • Experience technical writing in the medical device or other regulated industry
  • Strong collaboration skills
  • Strong problem-solving 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
  • Bachelors degree plus 2-5 years of related experience


Preferred Qualifications
  • Experience with a content management system or labeling system
  • Experience with desktop publishing tools, preferably InDesign and other Adobe tools
  • Ability to operate within complex processes
  • Experience in technical writing used for translated documentation


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