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Online Biotech Technical Writer Jobs (NOW HIRING)

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Technical Writer

Springfield, NJ · On-site

Experience: * Minimum of 2 years of experience in technical writing within a GMP-regulated environment in the pharmaceutical, biotech, or related industry. * Experience writing technical ...

Trax USA Corp.

Technical Writer

Coral Gables, FL

Technical Writers are responsible for providing effective information for end users and must be ... various Online Help libraries. These libraries include operational process flows and end user ...

Trax USA Corp

Technical Writer

Coral Gables, FL · On-site

Technical Writers are responsible for providing effective information for end users and must be ... various Online Help libraries. These libraries include operational process flows and end user ...

Integrated Resources INC

Technical Writer

Irving, TX

Writes, organizes, enters and compiles online help files to support end users. Creates, compiles ... Technical Recruiter Integrated Resources, Inc. IT Life Sciences Allied Healthcare CRO Certified MBE ...

Sidram Technologies

Technical Writer

Santa Clara, CA · On-site

Technical Writer Location: Santa Clara, CA Customer: J&J JD: Key Responsibilities * Bachelor ... Write and update user guides, manuals, and online help documents * Review content for clarity ...

Trax

Technical Writer

Coral Gables, FL · On-site

Technical Writers are responsible for providing effective information for end users and must be ... various Online Help libraries. These libraries include operational process flows and end user ...

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All JobsOnline Biotech Technical Writer Jobs

Online Biotech Technical Writer information

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$13

$38

$66

How much do online biotech technical writer jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for online biotech technical writer in the United States is $38.94, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $47.12 per hour, depending on experience, location, and employer.

What is the difference between Online Biotech Technical Writer vs Laboratory Scientist?

AspectOnline Biotech Technical WriterLaboratory Scientist
Required CredentialsBachelor's degree in life sciences, strong writing skillsBachelor's or higher in biology, chemistry, or related field
Work EnvironmentRemote, office-based, or hybridLaboratory setting, research facilities
Employer & Industry UsageBiotech companies, pharma, research organizationsResearch labs, biotech firms, academic institutions

The Online Biotech Technical Writer primarily creates scientific documentation and communicates complex biotech concepts in written form, often remotely. In contrast, Laboratory Scientists conduct experiments and research directly in lab settings. While both roles require a background in life sciences, their work environments and daily tasks differ significantly, with technical writers focusing on documentation and communication, and scientists on experimental work.

What cities are hiring for Online Biotech Technical Writer jobs?

Cities with the most Online Biotech Technical Writer job openings:

What are the most commonly searched types of Biotech Technical Writer jobs?

The most popular types of Biotech Technical Writer jobs are:

What states have the most Online Biotech Technical Writer jobs?

States with the most job openings for Online Biotech Technical Writer jobs include:

Online Biotech Technical Writer jobs near you

Technical Writer

Stark Pharma Solutions Inc

Swiftwater, PA • On-site

Contractor

Re-posted 8 days ago

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.