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Medical Device Technical Writer Jobs (NOW HIRING)

Three Point Solutions

Technical Writer

Northridge, CA · On-site

$20 - $22/hr

Medical Device Manufacturing Company Duration: 6 Months (Possible Extension) Location: Northridge, CA / Remote Shift: 1st Shift Responsibilities: * Create, edit, and maintain technical documents ...

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 ...

Core4ce

Technical Systems Analyst/Writer

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Work closely with network engineers, clinical engineers, medical device security teams, software ... Technical Writing: Exceptional written communication skills with the ability to translate complex ...

Core4ce Careers

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Work closely with network engineers, clinical engineers, medical device security teams, software ... Technical Writing: Exceptional written communication skills with the ability to translate complex ...

Orion Group

$33 - $38/hr

Senior Technical Writer - Quality Documentation & Change Control Location: 100% Onsite- Branchburg ... Pharmaceutical / Medical Device / Biotechnology Contract through the end of 2026 with potential ...

Actalent

Technical Writer II

San Diego, CA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Job Title: Technical Writer II The Technical Writer II supports manufacturing operations by ... regulated medical device organization. This role works closely with Manufacturing, Process ...

Actalent

Technical Writer II

San Diego, CA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Job Title: Technical Writer II The Technical Writer II supports manufacturing operations by ... regulated medical device organization. This role works closely with Manufacturing, Process ...

Automated Systems, Inc.

Be Seen First

GMP Technical Writer

Kenosha, WI · On-site

$60 - $75/hr

  • Medical

  • Dental

  • PTO

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

The Contingent Plan

Technical Writer II

San Diego, CA · On-site

  • Medical

  • Dental

  • Vision

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 Aug 19, 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 is a medical device technical writer?

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.

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 are the key skills and qualifications needed to thrive as a medical device technical writer?

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.

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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 August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.

Technical Writer

Three Point Solutions

Northridge, CA • On-site

$20 - $22/hr

Contractor

Posted 15 days ago

Job description

Job Title:         Technical Writer

Client:              Medical Device Manufacturing Company
Duration:         6 Months (Possible Extension)
Location:         Northridge, CA / Remote
Shift:                1st Shift

Responsibilities:

  • Create, edit, and maintain technical documents, manuals, work instructions, and procedures.
  • Review and update documentation to reflect product and process changes.
  • Collaborate with Engineering, Quality, Regulatory, and Manufacturing teams.
  • Organize technical information into clear, user-friendly documentation.
  • Ensure documents comply with company standards and regulatory requirements.
  • Support document control, version management, and revision activities.
  • Proofread documents for grammar, formatting, consistency, and technical accuracy.
  • Prepare patient-facing and medical device documentation when required.
  • Maintain accurate documentation and support continuous process improvements.

Required Qualifications:

  • Bachelor's degree required.
  • Experience writing technical or patient-facing documentation.
  • Strong written and verbal communication skills.
  • Excellent attention to detail and organizational skills.
  • Proficiency in Microsoft Word, Excel, Outlook, and PowerPoint.

Preferred Qualifications:

  • Experience in the medical device or regulated industry.
  • Knowledge of document control and quality management systems.
  • Ability to work independently and collaborate with cross-functional teams.
  • Strong editing, proofreading, and technical writing skills.

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