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Seasonal Medical Device Technical Writer Jobs (NOW HIRING)

Superbeo

Technical Writer

New York, NY · On-site

Technical Writer Job location: New York City, New York Job Duration: 3 Months, Contract to Hire ... Writing experience in the medical device industry or any relevant industry * Experience in writing ...

Actalent

Technical Writer

Irvine, CA · On-site

$35 - $40/hr

Technical Writer This role focuses on designing, writing, and publishing high-quality technical ... Experience supporting new product development projects in the medical device industry. * Exposure ...

Medtronic

Technical Writer

Moundsview, MN · On-site

In this exciting role as a Technical Writer , you will produce customer-facing product ... Plan, research, develop, and write medical device labeling, and manage labeling deliverables as ...

New

Philips

Lead Technical Writer

New Kensington, PA

$117K - $186K/yr

Job TitleLead Technical Writer Lead Technical Writer (New Kensington, PA) The Lead Technical Writer ... You've acquired 8+ years of experience in medical device labeling. * Your skills include attention ...

Philips

Lead Technical Writer

New Kensington, PA · On-site

$117K - $186K/yr

Job Title Lead Technical Writer Lead Technical Writer (New Kensington, PA) The Lead Technical ... You've acquired 8+ years of experience in medical device labeling. * Your skills include attention ...

ASI Systems Engineering

GMP Technical Writer

Tampa, FL · On-site

$60 - $70/hr

GMP Technical Writer Contract: 5 months duration with potential for extension Location: Tampa, FL ... or medical-device manufacturing * Demonstrated experience authoring SOPs, WorkInstructions ...

Robert Half

Technical Writer

Broomfield, CO · On-site

$47.50 - $55/hr

Background supporting documentation within engineering, manufacturing, laboratory, software, medical device, aerospace, semiconductor, or similar technical environments. * Strong writing, editing ...

The Contingent Plan

Technical Writer II

San Diego, CA · On-site

Pharmaceutical and/or medical device experience preferred. * Understanding of cGMP, ISO13485, and regulatory requirements * Three years of experience working as a technical writer. * Project ...

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Seasonal Medical Device Technical Writer information

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How much do seasonal medical device technical writer jobs pay per hour?

As of Aug 2, 2026, the average hourly pay for seasonal medical device technical writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.
What cities are hiring for Seasonal Medical Device Technical Writer jobs? Cities with the most Seasonal Medical Device Technical Writer job openings:
What are the most commonly searched types of Medical Device Technical Writer jobs? The most popular types of Medical Device Technical Writer jobs are:
What states have the most Seasonal Medical Device Technical Writer jobs? States with the most job openings for Seasonal Medical Device Technical Writer jobs include:
Seasonal Medical Device Technical Writer jobs near you

Technical Writer (Medical Devices)

LS Solutions, Inc.

Lafayette, CO • On-site

Other

Posted 18 days ago

Job description

Position Overview

We are seeking an experienced Technical Writer to support the CST Technical Communications team in creating and maintaining high-quality documentation for regulated medical devices. The primary focus of this role is authoring and revising Instructions for Use (IFUs) and electronic IFUs (eIFUs) using structured authoring tools and content management systems.

The ideal candidate will have experience with structured XML authoring, medical device documentation, and quality system processes while collaborating with cross-functional teams to deliver documentation that meets regulatory and project requirements.

Key Responsibilities
  • Author, update, and maintain Instructions for Use (IFUs) and electronic IFUs (eIFUs) using structured XML (DITA-like) authoring.
  • Create and manage technical documentation using Structured FrameMaker and Content Management Systems (CMS).
  • Perform change impact/effect analysis for documentation updates.
  • Support translation and localization review processes.
  • Manage documentation through CMS and quality system publishing workflows.
  • Collaborate with Engineering, Regulatory Affairs, Quality Assurance, Software, and Packaging teams to ensure accurate and compliant documentation.
  • Research technical information and translate complex concepts into clear, user-friendly documentation.
  • Develop and maintain operational manuals, instructional guides, maintenance procedures, and technical publications.
  • Ensure all documentation complies with company quality standards and regulatory requirements.
  • Support documentation activities throughout the medical device product lifecycle.
Required Qualifications
  • Bachelor''''''''s Degree.
  • 5+ years of Technical Writing experience.
Required Technical Skills
  • Structured content authoring (HTML, XML, DITA, or similar)
  • Structured FrameMaker
  • Adobe FrameMaker
  • Professional publishing tools
  • Content Management Systems (CMS)
  • IFU (Instructions for Use) development
  • Medical device technical documentation
  • Quality system documentation processes
  • Change effect/impact analysis
  • Requirements traceability
  • Translation and localization workflows
Preferred Skills
  • Adobe Illustrator
  • Adobe InDesign
  • Adobe Photoshop
  • Vasont Content Management System (CMS)
  • Experience within the medical device industry or another regulated industry

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