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Medical Technical Writer Jobs (NOW HIRING)

Marotta Controls, Inc.

Technical Writer

Parsippany, NJ

$75K - $100K/yr

Technical Writer, Configuration Management Overview We are seeking a Technical Writer to develop ... medical, prescription, dental, vision, life and disability income insurance programs, 401k ...

GXM Technologies LLC

Technical Writer

Colorado Springs, CO · Hybrid

$95K - $135K/yr

Description GXM is seeking a Technical Writer to support the development, maintenance, and delivery ... eligibility + medical/dental/vision/STD/LTD/Life + 401(k) + PTO Equal Employment Opportunity ...

Marotta Controls, Inc.

Technical Writer

Parsippany, NJ

$75K - $100K/yr

The Technical Writer will create and maintain technical documentation to support new product ... These include medical, prescription, dental, vision, life, and disability insurance, a 401(k) plan ...

Guidehouse

Technical Writer

Huntsville, AL · On-site

The Technical writer will have a background in areas of design, engineering, and construction ... Medical, Rx, Dental & Vision Insurance * Personal and Family Sick Time & Company Paid Holidays

Guidehouse

Technical Writer

Huntsville, AL

The Technical writer will have a background in areas of design, engineering, and construction ... Medical, Rx, Dental & Vision Insurance * Personal and Family Sick Time & Company Paid Holidays

Ridge Corporation

Technical Writer

Frazeysburg, OH

$19/hr

Technical Writer Location: Frazeysburg, OH Schedule: Monday-Friday 6am-2:30pm Pay: $19.00/hr ... 30 days (medical, dental, vision, disability, etc.) 4. 401(k) with company match + immediate ...

SAS

Technical Writer

Cary, NC · On-site

Technical Writer- Hybrid in Cary, North Carolina or Remote in NC We're a leader in data and AI ... Medical plan options include: * PPO with low annual deductible and copays. * HDHP combined with a ...

New

OptiTrack

Technical Writer

Seattle, WA · On-site

Job Summary: The Technical Writer is responsible for creating, maintaining, and improving ... Benefits All benefits start on first day of employment! * 75% employer-paid medical for employee.

OptiTrack

Technical Writer

Los Angeles, CA

Job Summary: The Technical Writer is responsible for creating, maintaining, and improving ... Benefits All benefits start on first day of employment! * 75% employer-paid medical for employee.

OptiTrack

Technical Writer

Corvallis, OR · On-site

Job Summary: The Technical Writer is responsible for creating, maintaining, and improving ... Benefits All benefits start on first day of employment! * 75% employer-paid medical for employee.

Medtronic

Technical Writer

Moundsview, MN · On-site

In this exciting role as a Technical Writer , you will produce customer-facing product ... Plan, research, develop, and write medical device labeling, and manage labeling deliverables as ...

OptiTrack

Technical Writer

Corvallis, OR · On-site

Job Summary: The Technical Writer is responsible for creating, maintaining, and improving ... Benefits All benefits start on first day of employment! * 75% employer-paid medical for employee.

OptiTrack

Technical Writer

Denver, CO · On-site

Job Summary: The Technical Writer is responsible for creating, maintaining, and improving ... Benefits All benefits start on first day of employment! * 75% employer-paid medical for employee.

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Medical Technical Writer information

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How much do medical technical writer jobs pay per hour?

As of Jun 29, 2026, the average hourly pay for medical 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 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.

How to get into medical technical writing?

Medical technical writers create clear, accurate documentation for healthcare and medical products, often requiring a background in life sciences or healthcare. Gaining skills in scientific writing, understanding medical terminology, and familiarity with tools like Microsoft Word and document management systems are essential; certifications such as the Certified Medical Publication Professional (CMPP) can also enhance job prospects.

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.

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.

Is there a demand for medical writers?

Medical technical writers are in high demand due to the need for clear, accurate communication of complex medical information in pharmaceuticals, healthcare, and regulatory documentation. The field offers opportunities across pharmaceutical companies, biotech firms, and healthcare organizations, often requiring knowledge of medical terminology and proficiency with tools like document management systems.

What is a medical technical writer?

A medical technical writer creates clear, accurate documentation such as clinical trial reports, regulatory submissions, and medical device instructions. They combine knowledge of medicine, science, and technical writing skills, often using tools like Microsoft Word and Adobe Acrobat, and may require familiarity with regulatory standards like FDA or ISO guidelines.

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.

Do medical writers make a lot of money?

Medical technical writers typically earn competitive salaries that vary based on experience, education, and location. Entry-level positions may start around $60,000 annually, while experienced writers with specialized knowledge can earn over $100,000. Skills in scientific writing, regulatory knowledge, and familiarity with tools like document management software can influence earning potential.
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Medical Technical Writer jobs near you

Technical Writer

Stark Pharma Solutions Inc

Swiftwater, PA • On-site

Contractor

Posted 20 days ago

Key responsibilities

  • Develop, revise, and maintain technical documentation, training materials, and process-related content.

  • Review, edit, and update quality documents including Standard Operating Procedures, Work Instructions, Guidelines, Validation Master Plans, and Quality System Documentation.

  • Collaborate with cross-functional teams to gather information and create compliant documentation and training materials for digital platform implementation.

Job description

Hi,

My name is Karthik Mutyala, and I am a Recruitment Manager with Stark Pharma Solutions, specializing in opportunities across the Pharmaceutical, Biotechnology, Medical Device, and Life Sciences industries.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

You can also follow Stark Pharma Solutions on LinkedIn for the latest job updates:

https://www.linkedin.com/company/99455976/

Role: Technical Writer

Location: Swiftwater, PA

Duration: 6-Month Contract

Industry: Pharmaceutical / Biotech Manufacturing

Position Overview

We are seeking a Technical Writer to support the implementation of a new digital platform by developing, updating, and converting technical and quality-related content into user-friendly training materials and documentation. This role will work closely with cross-functional teams to create compliant documentation, training content, and process materials within a GMP-regulated environment.

The ideal candidate will have experience in technical writing, quality systems documentation, and digital system deployments within pharmaceutical, biotechnology, laboratory, or manufacturing environments.

Key Responsibilities

  • Develop, revise, and maintain technical documentation, training materials, and process-related content.
  • Convert technical and operational information into engaging training presentations, user guides, and instructional materials.
  • Review, edit, and update quality documents including:
  • Standard Operating Procedures (SOPs)
  • Work Instructions
  • Guidelines
  • Validation Master Plans
  • Quality System Documentation
  • Ensure all documentation complies with GMP, regulatory, and internal quality requirements.
  • Collaborate with Quality, IT, Laboratory, and Operations teams to gather information and create accurate documentation.
  • Support digital transformation initiatives by developing training materials for new system implementations.
  • Assist with document control activities and quality documentation updates.
  • Create visual content, process flows, diagrams, and presentations using PowerPoint and Visio.
  • Participate in training development and delivery activities as needed.

Required Qualifications

  • Bachelor's degree required; advanced degrees (Master's or PhD) are welcome.
  • Minimum 2+ years of experience in Technical Writing, Documentation Management, or a related role.
  • Experience working within GMP-regulated pharmaceutical, biotech, laboratory, or life sciences environments.

Hands-on experience with quality systems and applications such as:

  • Veeva
  • LIMS
  • LabWare (preferred)

Proficiency with:

  • Microsoft Word
  • Excel
  • PowerPoint
  • Visio
  • Outlook
  • Strong technical writing, editing, and document management skills.
  • Excellent verbal and written communication abilities.
  • Strong interpersonal skills with the ability to work effectively in cross-functional teams.