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Full Time Biotech Technical Writer Jobs in Indiana

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 ...

The Lead Technical Writer will coordinate the efforts of the Technical Writing team, provide QA/QC ... Job Type: Regular Full Time Benefits: * Medical, Dental, and Vision Insurance * Health Savings ...

New

Technical Writer

Crane, IN · On-site

$100K - $120K/yr

Crane, IN Job Type: Full-Time Target Salary Range*: $100,000 - $120,000. *This represents the ... For this Technical Writer position, you will be responsible for producing, proof-reading, editing ...

... Full time Description & Requirements Shape the future of defense with MANTECH! Join a team ... MANTECH seeks a motivated, career and customer-oriented Technical Writer II to join our team in ...

Communications Schedule: Full-Time Shift: Day Job Travel: Yes - 10% of the time Minimum Clearance ... ORA_ON_SITE Description The Senior Technical Writer will support Naval Air Systems Command (NAVAIR ...

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Full Time Biotech Technical Writer information

What is the difference between Full Time Biotech Technical Writer vs Full Time Medical Writer?

AspectFull Time Biotech Technical WriterFull Time Medical Writer
CredentialsBachelor's degree in life sciences, writing experienceAdvanced degree (MD, PhD), medical/scientific background
Work EnvironmentBiotech companies, research labs, CROsPharmaceutical companies, medical communications firms
Industry UsageDevelops technical documentation for biotech productsCreates clinical, regulatory, and medical education content

Full Time Biotech Technical Writers focus on creating technical documents related to biotech products, often with a background in life sciences. Full Time Medical Writers typically have advanced medical or scientific degrees and produce clinical and regulatory content for the medical and pharmaceutical industries. While both roles require strong writing skills, their focus areas and required credentials differ significantly.

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 Full Time Biotech Technical Writer jobs?

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

Infographic showing various Full Time Biotech Technical Writer job openings in Indiana as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

GMP Technical Writer

Genovice

Indianapolis, IN • Hybrid

$70K - $100K/hr

Full-time

Posted 16 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.