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Medical Device Technical Writer

Actalent

Littleton (CO)

Remote

USD 70,000 - 100,000

Full time

Yesterday
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Job summary

A leading company is seeking a Medical Device Technical Writer to create and modify technical content while ensuring compliance with regulatory standards. This remote role requires extensive experience in medical writing and technical documentation in the medical device sector.

Benefits

401(k) Matching Contribution
Comprehensive Medical, Dental, and Vision Plans
Wellness Programs
Paid Vacation and Sick Time
Life Insurance and Disability Coverage

Qualifications

  • 7+ years of experience in medical technical writing.
  • Strong command of XML-based content management systems.
  • Proven ability to write for global audiences.

Responsibilities

  • Produce technical content by writing new material and editing existing content.
  • Manage all phases of content development projects, including needs assessment and deliverables.
  • Stay current with regulations and standards applicable to assigned products.

Skills

Technical Writing
Medical Devices
XML-based CMS

Job description

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Job Title: Medical Device Technical Writer

Job Description

As a Technical Writer, you will collaborate with internal customers and subject matter experts to produce technical content of moderate to high complexity, supporting assigned product lines. You will create and modify content, manage it within a content management system, and ensure it adheres to design control documents and regulatory standards.

Responsibilities

  • Produce technical content by writing new material, editing existing content, and gathering correct information from the content management system.
  • Apply metadata to content and verify it against lower-level requirements and product acceptance criteria.
  • Complete design control documents and verify content prior to release.
  • Manage all phases of content development projects, including needs assessment, deliverables, timelines, content management, review schedules, and release activities.
  • Report on project status, anticipate potential difficulties, and alert managers and internal customers.
  • Maintain art, photo, electronic, and printed document files to meet departmental and regulatory requirements.
  • Stay current with regulations and standards applicable to assigned products.
  • Conduct gap assessments of content to ensure compliance with FDA standards and regulations.

Essential Skills

  • 7+ years of experience in medical technical writing.
  • Strong command of XML-based content management systems.
  • Proven ability to write for global audiences.
  • Expertise in technical writing, regulatory standards, and medical devices.

Additional Skills & Qualifications

  • Experience with SOP and engineering documentation.
  • Familiarity with CMS platforms.
  • HML experience preferred.

Pay and Benefits

The pay range for this position is $70000.00 - $100000.00/yr.

Target Bonus on Base: 7.0%

At Terumo Blood and Cell Technologies, we provide competitive total reward offerings that consist of compensation, benefits, recognition, along with a wealth of other well-being, work-life and recognition programs which support in unlocking the potential for you and your family. Included in our expansive list of benefits offerings are multiple group medical, dental and vision plans, a robust wellness program, life insurance and disability coverages, also a variety of voluntary programs such as group accident, hospital indemnity, critical illness, pet insurance and much more. To help you save for retirement, we offer a 401(k) plan with a matching contribution and for work-life balance we have vacation and sick time programs for associates. For us, it’s about protecting the personal welfare of our associates and their families, helping to achieve personal goals and offering those extra touches for convenience, security and overall peace of mind.

Workplace Type

This is a fully remote position.

Application Deadline

This position is anticipated to close on Jul 10, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Seniority level
  • Seniority level
    Mid-Senior level
Employment type
  • Employment type
    Full-time
Job function
  • Job function
    Marketing, Public Relations, and Writing/Editing
  • Industries
    Entertainment, Design, and Fine Art

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