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On Call Medical Technical Writer Jobs (NOW HIRING)

Marotta Controls, Inc.

Technical Writer

Parsippany, NJ · On-site

$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 ...

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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On Call Medical Technical Writer information

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How much do on call medical technical writer jobs pay per hour?

As of Jun 30, 2026, the average hourly pay for on call 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 are the most commonly searched types of Medical Technical Writer jobs? The most popular types of Medical Technical Writer jobs are:
On Call 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.