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Director Biotech Technical Writer Jobs (NOW HIRING)

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Associates degree in Technical Writing, Journalism, Education, Communications, Engineering ... Clear Communication Company Description We are a growing biotechnology company in Athens, Georgia.

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Associates degree in Technical Writing, Journalism, Education, Communications, Engineering ... Clear Communication Company Description We are a growing biotechnology company in Athens, Georgia.

New

Urgent

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 ...

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 ...

Experience supporting pharmaceutical, biotechnology, medical device, food manufacturing, or similar ... Requests for accommodation related to our application process can be directed to the Kelly Human ...

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

As of Aug 23, 2026, the average hourly pay for director 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.

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Technical Writer

Stark Pharma Solutions Inc

Swiftwater, PA • On-site

Contractor

Re-posted 15 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.