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Freelance Biotech Technical Writer Jobs (NOW HIRING)

FreeUp

Remote Blog Writer

Saint Petersburg, FL · On-site +1

$20 - $30/hr

FreeUp is a freelance marketplace dedicated to connecting business owners with talented freelancers ... more technical accessible to our readers. Please have at least 3 samples of writing you've done ...

FreeUp

Remote Blog Writer

Saint Petersburg, FL · On-site +1

$20 - $30/hr

FreeUp is a freelance marketplace dedicated to connecting business owners with talented freelancers ... more technical accessible to our readers. Please have at least 3 samples of writing you've done ...

INCOG

Tech Writer - Tech Services

Fishers, IN · On-site

... in technical writing, preferably in a GMP environment or pharmaceutical/biotechnology industry * Strong writing skills with ability to create clear, concise, and accurate technical documentation

Solomon Page

Freelance Technical Designer

Manhattan, NY · On-site

$41/hr

We are hiring a Freelance Technical Designer for a top fashion/retail company in NYC! * Pay: $41/Hr ... Maintain fit standards, written reports, records and samples. * Create and maintain tracking ...

PSG Global Solutions

Medical Writer

Chesterfield, MO · On-site

... biotechnology and medical companies. As specialists in recognising talent we pride ourselves on not ... Create drafts of new technical or regulatory documents using existing examples, templates or ...

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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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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 Investigation Writer

System One

Lincolnton, NC • On-site

$40/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Posted 19 days ago

Job description

Job Title: Technical Investigation Writer Location: Lincolnton, NC Type: Contract Compensation: up to $40.00 per hour Work Model: ONSITE Hours: 40 hours M-F

Responsibilities

  • Investigate the quality deviations observed during raw material dispensing / manufacturing / packaging operations.
  • Review GMP documents such as SOPs, Batch records, Logbooks to identify the root cause for the reported deviation using Kepner-Tregoe, Ishikawa, Fish bone, 5 Why methods.
  • Partner with Technical Services, Engineering and Manufacturing team members to determine the scope, impact and risk associated with the deviations/non-conformances observed in Manufacturing and Packaging department.
  • Work with QA Compliance team members to finalize investigation reports and identify necessary CAPA for the reported deviation/non-conformance in timely manner.
  • Ensure timely implementation of CAPA resulting from deviations, customer complaints, Internal Audits.
  • Monitor and ensure closure of all open deviations/non-conformances and CAPAs within defined timeframes.
  • Review deviation trend to determine and propose appropriate actions needed to prevent reoccurrence of similar events.
  • Review and revise GMP documents (SOPs/Work Instructions/Productions Records, etc.)

Requirements

  • Bachelor's degree in Pharmacy, Chemistry, Biochemistry, Chemical Engineering, Life Sciences, or a related scientific discipline.
  • Minimum 3-5 years of experience in Pharmaceutical, Biotechnology, Medical Device, or other regulated GMP manufacturing environments.
  • Proven experience conducting and documenting deviation, non-conformance, and quality investigations.
  • Experience authoring and reviewing investigation reports, CAPAs, SOPs, batch records, and other GMP documentation.
  • Experience working in Manufacturing, Packaging, Quality Assurance, Quality Systems, or Technical Services functions.
  • Strong understanding of current Good Manufacturing Practices (cGMP), FDA regulations, and applicable industry standards.
  • Working knowledge of manufacturing, packaging, and raw material dispensing operations.
  • Understanding of Quality Management Systems (QMS), including deviations, investigations, change controls, CAPAs, and audit management.
  • Familiarity with risk assessment methodologies and quality compliance requirements.
  • Demonstrated expertise in conducting thorough investigations of manufacturing and packaging deviations.

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

#M3 Ref: #558-Scientific