Senior Medical Device Technical Writer

Equiliem; Saint Paul (MN); On-site; USD 69,000 - 77,000; Full time

Benefits offered by this job

Medical Insurance

Vision & Dental Insurance

Life Insurance

Matching 401(k)

Commuter Benefits

Employee Discounts & Rewards

Payroll Payment Options

Job summary

Equiliem seeks a Technical Writer IV to develop, edit, and maintain medical device documentation, including IFUs and external clinician/patient materials. The role collaborates with engineering, regulatory, marketing, and clinical teams to ensure accuracy and regulatory compliance.

Candidates should have 2–6+ years in medical device documentation, experience with document control systems, and familiarity with Windchill.

Qualifications

• 2–6+ years in technical writing within medical device/pharma/biotech.
• Experience writing external end-user documentation for patients or clinicians.
• Experience releasing controlled documentation via a document control system.
• Familiarity with Windchill or other PLM systems.
• Understanding of medical device labeling and regulatory practices.

Responsibilities

• Research, write, edit, and maintain technical documentation for new and sustaining product development projects.
• Develop instructions for use, patient manuals, clinician manuals, and other external end-user documentation.
• Collaborate with engineering, marketing, regulatory affairs, clinical teams, and other stakeholders to gather information and validate content.
• Ensure documentation meets regulatory labeling requirements and internal quality procedures.
• Create, revise, review, and release controlled documentation using document control and content management systems.
• Use content management tools (AIT or Vasont) and PLM systems (Windchill) as applicable.
• Manage multiple documentation projects with deadlines and quality expectations.
• Follow internal processes and documentation standards.
• Learn and apply new tools and workflows as required.
• Maintain high accuracy, consistency, and attention to detail throughout the lifecycle.

Skills

Technical writing

Editing

Research

Documentation management

Cross-functional collaboration

Attention to detail

Education

Bachelor's degree

Tools

AIT

Vasont

Windchill

Job description

Equiliem seeks a Technical Writer IV to develop, edit, and maintain medical device documentation, including IFUs and external clinician/patient materials. The role collaborates with engineering, regulatory, marketing, and clinical teams to ensure accuracy and regulatory compliance.

Candidates should have 2–6+ years in medical device documentation, experience with document control systems, and familiarity with Windchill.