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Online Biotech Technical Writer Jobs in Indiana (NOW HIRING)

GMP Technical Writer

Indianapolis, IN · Hybrid

$70K - $100K/hr

Previous technical writing experience in a GMP-regulated pharmaceutical, biotechnology, or biopharmaceutical environment . * Strong experience developing and revising SOPs, work instructions ...

For this Technical Writer position, you will be responsible for producing, proof-reading, editing, and formatting technical documentation to include design specifications, manuals, on-line help ...

... biotechnology industries. Additional Preferences: Proficient in writing clear, concise, and accurate technical documentation. Strong understanding of GMP manufacturing processes and regulatory ...

Develops print and/or online publications or public presentations of results from research by ... Technical Writing Click here to learn more about Indiana University's Job Framework. Posting ...

Minimum of 3 years of technical writing experience, preferably within a regulated GMP environment, and ideally in pharmaceutical, biopharmaceutical, or biotechnology industries. Additional ...

... in technical writing, preferably in a GMP environment or pharmaceutical/biotechnology industry * Strong writing skills with ability to create clear, concise, and accurate technical documentation

About the Job The Varsity Tutors Live Learning Platform has thousands of students looking for online Technical Writing tutors nationally. As a tutor on the Varsity Tutors Platform, you'll have the ...

About the Job The Varsity Tutors Live Learning Platform has thousands of students looking for online Technical Writing tutors nationally. As a tutor on the Varsity Tutors Platform, you'll have the ...

About the Job The Varsity Tutors Live Learning Platform has thousands of students looking for online Technical Writing tutors nationally. As a tutor on the Varsity Tutors Platform, you'll have the ...

About the Job The Varsity Tutors Live Learning Platform has thousands of students looking for online Technical Writing tutors nationally. As a tutor on the Varsity Tutors Platform, you'll have the ...

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Online Biotech Technical Writer information

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

The most popular types of Biotech Technical Writer jobs in Indiana are:

What cities in Indiana are hiring for Online Biotech Technical Writer jobs?

Cities in Indiana with the most Online Biotech Technical Writer job openings:

GMP Technical Writer

Genovice

Indianapolis, IN • Hybrid

$70K - $100K/hr

Full-time

Posted 6 days ago


Job description

This is a remote position.

GMP Technical Writer – Engineering

Location: Indianapolis, IN / Remote Hybrid
Type: Contract
Travel/On-Site: Initial 1 week on-site in Indianapolis, followed by approximately 2–3 on-site days per month. Remaining work may be performed remotely.

Position Overview

Our client, a growing biopharmaceutical manufacturing organization, is seeking an experienced GMP Technical Writer to support the development, revision, and maintenance of GMP documentation. This role will primarily support the Engineering organization (approximately 75%), with additional support across other GMP functions as needed.

Responsibilities

  • Write, revise, and update GMP-controlled documentation.
  • Develop and maintain SOPs, work instructions, protocols, forms, and equipment/engineering documents.
  • Work with Engineering and other SMEs to translate technical processes into clear, compliant documentation.
  • Ensure documents align with GMP requirements and site documentation standards.
  • Support document remediation and updates as site needs evolve.
  • Approximately 25% of support may extend to other GMP functional groups.

Qualifications

  • Previous technical writing experience in a GMP-regulated pharmaceutical, biotechnology, or biopharmaceutical environment.
  • Strong experience developing and revising SOPs, work instructions, protocols, and other controlled documents.
  • Experience supporting Engineering, Facilities, Maintenance, Calibration, Equipment, or Validation documentation strongly preferred.
  • Strong understanding of GMP documentation practices and Good Documentation Practices (GDP).
  • Ability to work independently and collaborate effectively with technical SMEs.
  • Must be able to travel to Indianapolis for an initial one-week onboarding period and approximately 2–3 days per month thereafter.