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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 ...

Astrix Inc

Technical Writer I

Houston, TX · On-site

The largest device company in the world - with complementary businesses in Surgical and Vision Care Technical Writer I Location: Houston, TX Benefits: Medical, Dental, Holiday, PTO 401K matching ...

Actalent

Technical Writer

Irvine, CA

$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 ...

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 ...

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 ...

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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Medical Device Technical Writer information

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

As of Jul 28, 2026, the average hourly pay for 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 are the key skills and qualifications needed to thrive in the Medical Device Technical Writer position, and why are they important?

To thrive as a Medical Device Technical Writer, you need a deep understanding of medical terminology, regulatory standards, and technical writing best practices, typically supported by a degree in science, engineering, or technical communication. Familiarity with document management systems, authoring tools (such as Adobe FrameMaker or MadCap Flare), and knowledge of FDA or ISO documentation requirements are often essential. Exceptional attention to detail, strong organizational skills, and clear communication help writers collaborate effectively with engineers, clinicians, and regulatory teams. These skills and attributes ensure that complex medical device information is accurately documented, compliant with regulations, and accessible to diverse stakeholders.

What are the typical day-to-day responsibilities of a Medical Device Technical Writer?

As a Medical Device Technical Writer, your daily responsibilities usually include creating and revising user manuals, product instructions, and regulatory documentation for medical devices. You'll often collaborate closely with subject matter experts such as engineers, product managers, and quality assurance teams to gather technical details and ensure accuracy. You may also be involved in reviewing documents for compliance with industry regulations and standards, as well as participating in document audits or updates. The role requires balancing multiple projects and deadlines while ensuring all materials are clear, concise, and suitable for their intended audience.

What is a Medical Device Technical Writer job?

A Medical Device Technical Writer creates clear, accurate documentation for medical devices, including user manuals, regulatory submissions, and technical reports. They translate complex technical information into understandable content for various audiences, such as healthcare professionals, regulatory agencies, and end-users. This role requires knowledge of medical device regulations, engineering concepts, and technical writing standards. Strong attention to detail and collaboration with engineers, regulatory specialists, and subject matter experts are essential.

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What cities are hiring for Medical Device Technical Writer jobs? Cities with the most Medical Device Technical Writer job openings:
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Medical Device Technical Writer jobs near you
Infographic showing various Medical Device Technical Writer job openings in the United States as of July 2026, with employment types broken down into 77% Full Time, 14% Part Time, and 9% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.
Technical Writer (Medical Devices)

Technical Writer (Medical Devices)

LS Solutions, Inc.

Lafayette, CO • On-site

Other

Posted 13 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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