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Trainee Medical Device Technical Writer Jobs (NOW HIRING)

Scalence L.L.C.

Sr Technical Writer

Minneapolis, MN · On-site

C. is seeking an experienced Senior Technical Writer to develop and manage medical device labeling documentation for an ablation product line. The role involves creating and maintaining product ...

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 ...

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 ...

Sterling Engineering, Inc.

Be Seen First

Medical Device Sales Representative

San Francisco, CA · Remote

$80K/yr

Strong communication, negotiation, and proposal-writing skills * Self-motivated, coachable, and ... Prior medical device, technical product, or travel sales experience a plus. * Experience building ...

ASI Systems Engineering

GMP Technical Writer

Kenosha, WI · On-site

$60 - $75/hr

GMP Technical Writer Contract: 12 - 18 months duration Location: Kenosha County, WI. - onsite Role ... or medical device manufacturing • Demonstrated experience authoring Deviation reports, CAPA ...

Robert Half

Technical Writer

Broomfield, CO · On-site

$47.50 - $55/hr

... software, medical device, aerospace, semiconductor, or similar technical environments. • Strong writing, editing, proofreading, and verbal communication skills with the ability to present ...

Actalent

Medical Device Engineer

San Diego, CA · On-site

$50/hr

Technical writing experience supporting engineering or quality documentation. * Ability to perform ... Medical device industry experience preferred. * Experience with electrochemical test systems is ...

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

As of Jul 23, 2026, the average hourly pay for trainee 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 Trainee Medical Device Technical Writer jobs? Cities with the most Trainee 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 Trainee Medical Device Technical Writer jobs? States with the most job openings for Trainee Medical Device Technical Writer jobs include:
Trainee Medical Device Technical Writer jobs near you
Technical Writer (Medical Devices)

Technical Writer (Medical Devices)

LS Solutions, Inc.

Lafayette, CO • On-site

Other

Posted 8 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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