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Medical Technical Writer Jobs in Tennessee (NOW HIRING)

RbM Services, LLC

Technical Writer

Oak Ridge, TN · On-site

With over 100 years of combined experience in the medical device industry, our management staff has ... The Technical Writer/Protocol Development Specialist works with the engineering staff to document ...

iFixit

Junior Technical Writer

Chattanooga, TN · On-site

iFixit is currently seeking a Junior Technical Writer to create unparalleled repair documentation ... Employer-subsidized health insurance through Anthem Blue Cross including medical, dental, vision ...

iFixit

Junior Technical Writer

Chattanooga, TN · On-site

iFixit is currently seeking a Junior Technical Writer to create unparalleled repair documentation ... Employer-subsidized health insurance through Anthem Blue Cross including medical, dental, vision ...

iFixit

Junior Technical Writer

Chattanooga, TN · On-site

iFixit is currently seeking a Junior Technical Writer to create unparalleled repair documentation ... Employer-subsidized health insurance through Anthem Blue Cross including medical, dental, vision ...

LabConnect

Medical Writer

Johnson City, TN · On-site +1

The Medical Writer is responsible for authoring clinical trial and regulatory documents, through ... This role requires strategic thinking with exceptional scientific and technical writing skills ...

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All JobsMedical Technical Writer JobsMedical Technical Writer Jobs in Tennessee

Medical Technical Writer information

See Tennessee salary details

$12

$35

$52

How much do medical technical writer jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for medical technical writer in Tennessee is $35.07, according to ZipRecruiter salary data. Most workers in this role earn between $23.80 and $44.28 per hour, depending on experience, location, and employer.

What does a medical technical writer do?

As a medical technical writer, your job is to help create scientific documents that explain various aspects of health care and related technology to other people. In this role, you may define terminology, write an article based on guidelines set out by the buyer, or produce marketing or educational material. Medical technical writers often write for varying audiences, ranging from new medical students to highly-educated professionals. Therefore, the ability to understand the material and convince audiences you are an expert on the material is essential to this role. Some medical technical writers publish in professional medical journals instead of more broadly-available avenues.

What does a medical technical writer do?

A Medical Technical Writer creates clear, accurate, and concise documentation related to medical, scientific, or healthcare topics. Their work includes preparing regulatory submissions, clinical study reports, user manuals for medical devices, and educational materials for healthcare professionals or patients. They collaborate with scientists, researchers, and regulatory experts to ensure complex information is communicated effectively and complies with industry standards. Strong writing skills and an understanding of medical terminology are essential for this role.

What are the key skills and qualifications needed to thrive as a medical technical writer, and why are they important?

To thrive as a Medical Technical Writer, you need a solid background in life sciences or medicine, excellent written communication skills, and attention to detail, often supported by a degree in a relevant field. Familiarity with regulatory guidelines (such as FDA or EMA), reference management tools, and document management systems is typically required. Strong organizational skills, the ability to convey complex information clearly, and adaptability to fast-changing requirements distinguish outstanding professionals in this role. These skills ensure the production of accurate, compliant, and understandable medical documents essential for regulatory approval and effective communication within the healthcare industry.

What are some common challenges faced by medical technical writers when working with subject matter experts (SMEs)?

Medical Technical Writers often collaborate closely with subject matter experts such as physicians, researchers, and regulatory professionals. A common challenge is translating complex scientific or clinical information into clear, accurate, and regulatory-compliant documents while maintaining the intended meaning. Writers may also encounter tight deadlines or limited access to busy SMEs, requiring effective communication and project management skills. Building strong relationships and preparing well-structured questions can help streamline the review process and ensure high-quality deliverables.

What is the difference between Medical Technical Writer vs Medical Writer?

AspectMedical Technical WriterMedical Writer
CredentialsOften requires scientific or medical degrees, certifications like RAC or CCRTypically holds degrees in life sciences, journalism, or communications
Work EnvironmentPharmaceutical, biotech, or medical device companies, regulatory agenciesHealthcare publications, pharmaceutical marketing, academic journals
Employer & IndustryRegulatory, clinical research, medical device firmsMedical publishing, marketing, research organizations

Medical Technical Writers focus on creating regulatory documents, clinical trial reports, and technical materials, often requiring specialized scientific knowledge. Medical Writers produce a broader range of content, including marketing materials, journal articles, and patient education, with less emphasis on regulatory documentation. Both roles require strong writing skills and medical knowledge but differ mainly in their specific focus and work environment.

Are medical technical writers still in demand?

Medical technical writers are in steady demand due to the ongoing need for clear, accurate documentation in healthcare, pharmaceuticals, and medical device industries. They often require knowledge of medical terminology and proficiency with tools like Adobe FrameMaker or MS Word, and employment opportunities are available in both full-time and freelance roles.

Is there a demand for medical technical writers?

Medical technical writers are in demand due to the growing need for clear, accurate documentation in healthcare, pharmaceuticals, and medical device industries. They often require knowledge of medical terminology and proficiency with tools like Microsoft Word and Adobe FrameMaker, with opportunities available in both full-time and freelance roles.
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Medical Technical Writer jobs near you
Infographic showing various Medical Technical Writer job openings in Tennessee as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 12% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $72,939 per year, or $35.1 per hour.

Technical Writer

RbM Services, LLC

Oak Ridge, TN • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 5 days ago

Job description

About Us
Founded in 2000, locally owned and operated, RbM Services is a growing turn-key design, manufacture, and service solution provider for medical devices in Tennessee’s Technology Corridor. With over 100 years of combined experience in the medical device industry, our management staff has extensive experience in intellectual property development, contract design, product development, field service support, and product support of medical devices and laboratory instrumentation. Our team is passionate and even obsessed with providing solutions that deliver cutting-edge technology that improves patient experiences and outcomes. Our passion lies in the pursuit of perfection. We value our employee family and foster opportunities for us to engage in meaningful connections, and we reward employees who exceed expectations.
Job Description
The Technical Writer/Protocol Development Specialist works with the engineering staff to document design verification activities, engineering technical reports, and manufacturing/service procedures. This position will focus on creating comprehensive technical documentation and support record-keeping activities necessary in the world of medical device compliance.
Job Duties:
  • Document Engineering Design Activities
    1. Working with engineering staff to document project plans, inputs (requirements/specifications), design reviews, outputs, and verification and validation protocols and results
  • Development of Verification and Validation Protocols
    1. Working with engineering staff to plan how a set of requirements will be verified and validated.
    2. Outline the general approach to test each specific requirement.
    3. Develop the specific individual test steps for each specific requirement.
  • Release Engineering Technical Reports
    1. Incorporate engineering information into a standardized technical report format
  • Development and Maintenance of Engineering Library
    1. Develop and maintain a library of example images to use in manufacturing and servicing procedures.
Benefits
As a full-time team employee, you are eligible for all RbM Services benefits including medical, dental, vision, long-term, short-term disability, 401k, PTO, 10 paid holidays, etc.
All your information will be kept confidential according to the EEO guidelines.

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