Engineering - Technical Writer

Artech LLC

Minneapolis, MN

JOB DETAILS
SALARY
$45–$50 Per Hour
SKILLS
Change Control, Communication Skills, Corrective and Preventative Action (CAPA) Systems, Cross-Functional, Documentation, FDA (Food and Drug Administration), Implants, Maintain Compliance, Medical Equipment, Medical Terminology, Multitasking, Problem Solving Skills, Product Development, Product Lifecycle Management, Product Support, Project/Program Management, Prototyping, Quality Metrics, Regulations, Regulatory Compliance, Research & Development (R&D), Team Player, Technical Writing, Time Management, Traceability, User Documentation, Writing Skills
LOCATION
Minneapolis, MN
POSTED
30+ days ago

Job Title: Engineering - Technical Writer
Job ID: 24973
Location: Minneapolis Minnesota 55432
Duration:12 Months
Payrate: $45.00- $50.00 /HR. on W2


Key Requirements

  • Bachelor’s degree
  • 2–7 years of technical writing experience
  • Strong communication & collaboration skills

Top Skills (Must Have)

  • Technical Writing (user guides, IFUs, manuals)
  • Cross-functional collaboration
  • Quality & regulatory compliance (QMS)

Core Responsibilities

  • Develop and maintain labeling documentation (IFUs, user guides, implant manuals)
  • Write, edit, format, and prototype technical documents
  • Manage reviews, approvals, and change control
  • Ensure compliance with FDA, EU MDR, and quality standards
  • Collaborate with R&D, Quality, and cross-functional teams
  • Handle multiple projects and deadlines
  • Support labeling investigations and issue resolution

Nice to Have

  • Experience in:
    • Medical devices / regulated environment (FDA)
    • EU MDR regulations
    • CAPA / Quality processes
    • PLM tools
    • Medical terminology / neuromodulation

Work Scope

  • Create documentation for clinicians and patients
  • Support new product development and sustaining projects
  • Maintain traceability and compliance documentation

Top 3 Hiring Priorities

  1. Strong technical writing experience
  2. Experience with regulated documentation (FDA/EU MDR)
  3. Ability to manage multiple projects and collaborate cross-functionally

About the Company

A

Artech LLC