×
Register Here to Apply for Jobs or Post Jobs. X

Senior Technical Writer - Engineering

Job in Minneapolis, Hennepin County, Minnesota, 55400, USA
Listing for: Redbock - an NES Fircroft company
Contract position
Listed on 2026-07-08
Job specializations:
  • Engineering
    Research Scientist, Biomedical Engineer, Medical Device Industry
Salary/Wage Range or Industry Benchmark: 70000 - 90000 USD Yearly USD 70000.00 90000.00 YEAR
Job Description & How to Apply Below

Engineering
- Sr. Technical Writer (12 month contract // Minneapolis, MN):
Top 3

Skills:

  • Experience authoring IFUs, manuals and user guides
  • Experience with marketing and medical literature writing is preferred
  • Candidate will need to have strong communication and capability to function highly independently with limited guidance
Description:

As a Senior Technical Writer, you will support the development of customer-facing product labeling for an ablation product line. The labeling may include: instructions for use (IFU), manuals, user guides, device labels, and package labels. You may also work on marketing materials and medical literature. In addition to the labeling itself, you will be accountable for labeling supporting documentation, which may include design plans, requirements documents, review reports, and verification reports.

You will directly support R&D projects for both new product development and released product maintenance. We are seeking a highly independent, self-driven, and accountable technical writer with prior experience with medical device labeling and the regulatory process, who requires minimal supervision.

Key responsibilities include the following:
  • Set the strategy and develop plans for projects impacting the labeling for this product line.
  • Collaborate with departmental and cross-functional stakeholders and subject matter experts to develop the labeling content and resolve issues as they arise during the development process.
  • Ensure compliance of labeling with all applicable regulatory (e.g., FDA, EU MDR, ISO standards, etc.) and quality requirements.
  • Write and produce documentation that conforms to quality management system requirements.
  • Produce and/or edit graphics, illustrations, and charts that are included within the labeling materials.
  • Communicate project status and risks to program, functional, and business leaders.
  • Provide input to project schedule development.
  • Effectively manage multiple projects, changes in project scope, and shifting priorities to maintain project requirements and ensure deadlines are met.
Must Have:
  • Project Management
  • Self-driven, independent, and accountable
#J-18808-Ljbffr
Position Requirements
10+ Years work experience
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary