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Freelance Biotech Technical Writer Jobs (NOW HIRING)

Kinetic Personnel Group

Be Seen First

Technical Writer (ONSITE CONTRACT)

Tustin, CA · On-site

$45 - $60/hr

  • Medical

  • Dental

  • Vision

Experience in a biopharmaceutical, pharmaceutical, medical device, biotechnology, or other regulated manufacturing environment preferred. * Strong technical writing, editing, proofreading, and ...

New

Experic LLC

Technical Writer - Operations

Cranbury, NJ

$80K - $110K/yr

Bachelor's degree preferred in Life Sciences, Engineering, Technical Writing, or related field; equivalent experience may be considered. * 3+ years of experience in a pharmaceutical, biotechnology ...

24 Seven Talent

Technical Content Writer

Bayport, MN · On-site

$25 - $35/hr

Write and edit digital content for web, blog, and related channels. * Translate technical ... Experience through internships, freelance work, coursework, or student publications is a plus.

Kelly Services

Contract Technical Writer

Raleigh, NC

$40 - $47/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... biotech, medical device, or similar manufacturing environment. * Experience authoring and revising SOPs, batch records, work instructions, and laboratory documentation. * Working knowledge of CAPA ...

Aequor

Experience working in GMP pharma and/or biotechnology industry. Experience in a Good Manufacturing Practices (GMP) environment and demonstrated background in technical writing. Experience with device ...

New

Medpace, Inc.

Scientific Technical Writer

Cincinnati, OH · On-site +1

  • Medical

  • Retirement

  • PTO

... Technical Writer to join our team. If you want an exciting career where you use your previous ... biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the ...

Valnet Inc.

Freelance Tech Writer (Smart Home)

Nashville, TN · On-site +1

$20.50 - $26.25/hr

We're looking for Freelance Tech Writers to contribute feature content to our Smart Home category ... Explain technical concepts clearly for non-technical audiences * Test devices, platforms, or ...

System One

Technical Investigation Writer

Lincolnton, NC · On-site

$40/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Technical Investigation Writer Location: Lincolnton, NC Type: Contract Compensation: up to $40.00 ... Minimum 3-5 years of experience in Pharmaceutical, Biotechnology, Medical Device, or other ...

System One

Technical Investigation Writer

Lincolnton, NC · On-site

$40/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Technical Investigation Writer Location: Lincolnton, NC Type: Contract Compensation: up to $40.00 ... Minimum 3-5 years of experience in Pharmaceutical, Biotechnology, Medical Device, or other ...

System One

Technical Investigation Writer

Lincolnton, NC · On-site

$40/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Technical Investigation Writer Location: Lincolnton, NC Type: Contract Compensation: up to $40.00 ... Minimum 3-5 years of experience in Pharmaceutical, Biotechnology, Medical Device, or other ...

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Freelance Biotech Technical Writer information

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

As of Aug 13, 2026, the average hourly pay for freelance biotech technical writer in the United States is $23.27, according to ZipRecruiter salary data. Most workers in this role earn between $20.43 and $26.20 per hour, depending on experience, location, and employer.

What is the difference between Freelance Biotech Technical Writer vs Freelance Medical Writer?

AspectFreelance Biotech Technical WriterFreelance Medical Writer
CredentialsScientific background, life sciences degreeMedical or health sciences degree, clinical knowledge
Work EnvironmentBiotech companies, research labs, contract agenciesPharmaceutical firms, healthcare organizations, clinical research
Industry UsageBiotech, research, and development sectorsPharmaceuticals, clinical trials, healthcare communication
Common Search/ComparisonYesYes

Freelance Biotech Technical Writers focus on scientific and technical content related to biotechnology, while Freelance Medical Writers specialize in medical and clinical content. Both roles require scientific credentials and often work in similar environments, but their industry focus and target audiences differ.

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What states have the most Freelance Biotech Technical Writer jobs?

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Freelance Biotech Technical Writer jobs near you
Infographic showing various Freelance Biotech Technical Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 6% Part Time, 4% Contract, and 1% Nights. Highlights an 89% Physical, 4% Hybrid, and 7% Remote job distribution, with an average salary of $48,412 per year, or $23.3 per hour.

Technical Writer (Springfield, NJ)

Cedent

Springfield, NJ • On-site

Full-time

Re-posted 18 days ago

Job description

Summary: Reporting to the appropriate department based on area of expertise (Quality Assurance, Quality Control, or Manufacturing). We are seeking a detail-oriented and highly skilled GMP Pharmaceutical Technical Writer to join our team. The ideal candidate will be responsible for creating, revising, and maintaining various controlled documentation that complies with Good Manufacturing Practices (GMP) regulations and industry standards. This role will work closely with internal and client cross-functional teams, including quality assurance, regulatory, production, and project management, to ensure timely delivery, accuracy, and clarity of all technical documents essential for the manufacturing and regulatory processes in a pharmaceutical industry.
Responsibilities:
  • Technical Documentation: Author, edit, and maintain a wide range of documents, including Standard Operating Procedures (SOPs), batch records, validation protocols, technical reports, change control documents, and regulatory submissions in accordance with GMP guidelines.
  • Compliance: Ensure all written materials meet regulatory and GMP requirements, and align with the company's quality standards, procedures, and policies.
  • Collaboration: Work closely with both Client stakeholders and client stakeholders to establish alignment on deliverables and ensure project timelines are maintained.
  • Document Management: Assist in the management of controlled documents in document control systems (e.g., electronic document management systems), ensuring traceability, version control, and appropriate distribution of approved documents.
  • Process Improvement: Participate in process improvement initiatives related to document control, writing standards, and compliance, ensuring continuous enhancement of documentation practices.
  • Audits & Inspections: Support internal and external audits by preparing relevant documentation and ensuring that all technical writing adheres to current regulatory standards.
  • Change Control: Document and track changes in manufacturing processes, equipment, and methodologies, ensuring updates to procedures and records are properly reflected.
Essential Education and Qualifications:
  • Education: Bachelor's degree in Life Sciences, Chemistry, Pharmaceutical Sciences, Engineering, or a related field. Advanced degree or certification in technical writing is a plus.
  • 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 documentation, including SOPs, validation protocols, and reports.
  • Knowledge:
  • Solid understanding of GMP regulations (FDA, EMA, ISO, ICH, etc.) and regulatory requirements for pharmaceutical manufacturing.
  • Proficiency with document management systems and Microsoft Office Suite (Word, Excel, PowerPoint).
  • Skills:
  • Exceptional written and verbal communication skills, with a strong ability to translate complex technical concepts into clear, concise documentation.
  • Detail-oriented with strong organizational and project management skills.
  • Ability to work independently, manage multiple projects simultaneously, and meet deadlines in a fast-paced environment.
  • Strong analytical and problem-solving skills, with the ability to work cross-functionally across departments.
Cedent logo

About Cedent

Sourced by ZipRecruiter

CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008

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