2

Full Time Biotech Technical Writer Jobs in Indiana

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 ...

Technical Writer

Michigan City, IN · On-site

$77K - $85K/yr

Salary Full-Time Function: Marketing Pay Range: $77,065.30 - $85,093.29 Target Bonus: 10% ​ About ... Position Summary The Technical Writer is responsible for creating, revising, and maintaining high ...

Technical Writer

Michigan City, IN · On-site

$77K - $85K/yr

Salary Full-Time Function: Marketing Pay Range: $77,065.30 - $85,093.29 Target Bonus: 10% About us ... Position Summary The Technical Writer is responsible for creating, revising, and maintaining high ...

About the Position Clinical Architecture is seeking a Technical Writer in the Indianapolis, IN area ... Paid Volunteer Time, Paid Holidays & PTO, including our own winter break week for full-time team ...

About the Position Clinical Architecture is seeking a Technical Writer in the Indianapolis, IN area ... Paid Volunteer Time, Paid Holidays & PTO, including our own winter break week for full-time team ...

... 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 ...

Indianapolis Job Type: Full-time Classification: N-4 Salary Range: $18.00-$22.00 per hour Reports ... technical support during lab classes. * Train and supervise student assistants or interns in ...

next page

Showing results 1-20

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 July 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 100% In-person job distribution.

$100K - $120K/yr

Full-time

Re-posted 22 days ago


Job description

Security Clearance: Secret

Location: Crane, IN

Job Type: Full-Time

Target Salary Range*: $100,000 - $120,000.

*This represents the potential salary range for this position depending on education level, years of experience and/or certifications in addition to other position specific requirements which may impact salary

Position Overview:

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, procedures, plans, and proposals.

Key Responsibilities:

  • Edit and format information for consumption through various media channels to include printed materials, scripted voice content, email, websites, and other electronic access points.
  • Write technical [prototype] manuals, training manuals, and standard operating procedures for prototypes undergoing CONOP development.
  • Ensure that Technical Data Packages (TDPs) are prepared and delivered for assigned projects that reach the prototype or low-rate production stages of development. Assist in the development of the TDP.
  • Create and maintain basic briefs for various prototype devices and coordinate test event support and participate in planning meetings.
  • Prepare and deliver Test Plans and Test Results for both functional and operational tests for assigned projects.
  • Travel as needed to support test events. The contractor shall operate test units, monitoring devices, and associated equipment.
  • Interact with and coordinate prototype and low-rate production with external parties tasked with producing units for assigned projects.
  • Provide routine status updates and communicate urgent matters involving production issues to management and other stakeholders in a timely manner via phone, email, or other normal communication methods.
  • Manage inventory documentation for ordering and incoming material, and general organization of lab inventory.
  • Write lab SOPs for equipment, including Hazard Analysis of procedures. These are standard Crane SOPs and written to that standard.
  • Obtain and maintain certification in Hazard Analysis and Non-Ordnance SOP Writing via NSWC Crane offered training.
  • Demonstrate competent writing and oral communication skills.
  • Be a self-starter, capable of working with minimal oversight and have excellent written and verbal communication skills. Familiarity with technical concepts and terminology.
  • Focus on end-user’s needs and ensure the documentation is intuitive and easy to follow. Conduct usability testing and gather user feedback for continuous documentation improvement.
  • Manage documentation lifecycle and maintain documentation product updates/changes. Archive outdated documents and ensure the latest versions are readily available.
  • Utilize documentation tools and software to create and manage documents. Incorporate multimedia elements (videos, images, diagrams) to enhance understanding if/when applicable.

Qualifications:

  • A-BET accredited Bachelor’s Degree in STEM / technical / engineering discipline
  • Minimum 3 years of experience in a position requiring STEM / technical / engineering expertise
  • Eligibility for a SECRET clearance.
  • Experience prepping TDPs
  • Experience with Hazard Analysis
  • Excellent technical writing and data presentation skills
  • Track record of complex problem-solving aptitude
  • Ability to think analytically and independently
  • Team orientated
  • Excellent problem-solving skills
  • Ability to communicate clearly both orally and in written form
  • Willingness to learn new skills
  • Ability to work on multiple projects concurrently

Preferred Qualifications:

  • 5-10 years technical writing experience or other related technical field
  • Existing experience producing technical documentation for projects on IAC MAC task orders
  • Experience in a technical writing position working with IAC MAC customers
  • Experience in DoD customer relations and technical writing
  • Certified Professional Technical Communicator (CPTC)
  • Active minimum Secret clearance