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Manager Biotech Technical Writer Jobs (NOW HIRING)

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Technical Writer

Springfield, NJ

Document Management: Assist in the management of controlled documents in document control systems ... biotech, or related industry. * Experience writing technical documentation, including SOPs ...

RWDC Industries

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Technical Writer

Athens, GA · On-site

Certification or training in technical writing or quality management (e.g., ISO 9001, AS9100). Core ... Clear Communication Company Description We are a growing biotechnology company in Athens, Georgia.

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RWDC Industries

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Technical Writer

Athens, GA · On-site

Certification or training in technical writing or quality management (e.g., ISO 9001, AS9100). Core ... Clear Communication Company Description We are a growing biotechnology company in Athens, Georgia.

Urgent

Integrated Resources INC

Technical Writer

Cambridge, MA · On-site

Excellent communication skills including: technical writing, interpersonal and collaborative skills ... Biotech/Pharma industry, knowledge about FDA regulations is required Some document management ...

Genovice

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 ...

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Manager Biotech Technical Writer information

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

As of Aug 27, 2026, the average hourly pay for manager 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 Manager Biotech Technical Writer vs Biotech Technical Writer?

AspectManager Biotech Technical WriterBiotech Technical Writer
ResponsibilitiesOversees writing teams, manages project timelines, ensures regulatory complianceCreates and edits scientific documents, manuals, and reports
Required SkillsLeadership, project management, advanced scientific writingStrong scientific writing, research skills, attention to detail
ExperienceTypically 5+ years, leadership experience preferred2+ years in biotech or scientific writing
Work EnvironmentTeam management, cross-department collaborationIndividual contributor, primarily office-based

The main difference is that the Manager Biotech Technical Writer leads teams and manages projects, while the Biotech Technical Writer focuses on creating scientific content. The manager role involves leadership and oversight, whereas the technical writer role emphasizes writing and research skills.

What cities are hiring for Manager Biotech Technical Writer jobs?

Cities with the most Manager 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 Manager Biotech Technical Writer jobs?

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

Manager Biotech Technical Writer jobs near you

Technical Writer

Swiftwater, PA • On-site

Stark Pharma Solutions Inc
See more jobs at Stark Pharma Solutions Incexternal

Contractor

Re-posted 18 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.