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Technical Writer Biology Jobs (NOW HIRING)

Caresoft

Technical Writer

Rochester, NY · On-site

A minimum of an associate's degree in Technical Writing, Communications, Medical Technology, Biology or Engineering with technical writing experience or equivalent is required. A minimum of 3 years ...

Adecco

Technical Writer

High Point, NC · On-site

$20/hr

Biology * Biochemistry * Pharmaceutical Sciences * Or another related scientific discipline ... Strong scientific writing and technical documentation skills. Preferred Qualifications Experience ...

Lancesoft

Technical Writer

High Point, NC · On-site

$27/hr

Qualifications Education Bachelor's degree in Chemistry, Microbiology, Biology, Biochemistry ... Knowledge, Skills, and Abilities Advanced technical writing and documentation skills. Strong ...

Maxonic

Be Seen First

Technical Writer

Rockville, MD · On-site

$31/hr

Technical Writer Job Type: Contract Job Location: Rockville, MD Work Schedule: On-site Pay Rate ... Experience within cell/gene therapies, biologics, and/or cGMP regulated environment preferred

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How much do technical writer biology jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for technical writer biology 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 are some typical responsibilities of a Technical Writer Biology on a daily or weekly basis?

Technical Writers specializing in biology are often responsible for creating and editing scientific documents such as research articles, manuals, protocols, product documentation, and grant applications. In their daily work, they collaborate closely with scientists, researchers, and subject matter experts to gather accurate information and ensure content is clear, concise, and in compliance with industry standards. Weekly tasks may include revising drafts based on feedback, managing multiple documents simultaneously, and staying current with scientific advancements relevant to their projects. This role offers a dynamic blend of independent writing and teamwork in research labs, biotech companies, or academic settings.

What is a Technical Writer Biology job?

A Technical Writer in Biology creates clear, accurate, and well-structured documents related to biological sciences. They develop research papers, regulatory documents, user manuals, and instructional content for scientific audiences or the general public. This role requires strong writing skills, attention to detail, and an understanding of biological concepts. Technical Writers often collaborate with scientists, researchers, and regulatory professionals to ensure accuracy and compliance.

What are the key skills and qualifications needed to thrive in the Technical Writer Biology position, and why are they important?

To thrive as a Technical Writer Biology, you need a solid background in biology or life sciences combined with exceptional writing, research, and communication skills, often supported by a relevant degree. Familiarity with scientific publishing standards, referencing software, and tools like Microsoft Office, LaTeX, or content management systems is typically required. Attention to detail, the ability to translate complex scientific concepts into clear language, and strong organizational skills are invaluable soft skills in this role. These competencies ensure that technical and scientific information is both accurate and accessible for diverse audiences, meeting the needs of researchers, regulatory bodies, and the broader scientific community.

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Technical Writer Biology jobs near you
Infographic showing various Technical Writer Biology job openings in the United States as of July 2026, with employment types broken down into 76% Full Time, 21% Part Time, 1% Temporary, and 2% Contract. Highlights an 81% Physical, 1% Hybrid, and 18% Remote job distribution, with an average salary of $81,001 per year, or $38.9 per hour.
Technical Writer

Technical Writer

Indotronix International Corporation

High Point, NC • On-site

$20 - $27/hr

Full-time

Posted 18 days ago

Job description

Technical Writer | High Point, North Carolina, United States Technical Writer - Quality Control Investigation Writer (GMP, Pharma) Location: High Point, NC 27265 | Contract | 2-5 Years Experience About the Role Join a dynamic pharmaceutical Quality Control team as a QC Investigation Writer, where your technical writing expertise will drive compliance and contribute directly to patient safety. You'll be at the forefront of laboratory investigations, collaborating cross-functionally to ensure data integrity and regulatory excellence in a fast-paced, growth-oriented environment. Responsibilities - Lead, author, and coordinate complex laboratory investigations (OOS, OOT, EM, deviations) to support GMP manufacturing operations. - Analyze laboratory data, test methods, instrument records, and documentation to determine root causes and product impact. - Facilitate investigation meetings with QC analysts, Microbiology, QA, and Manufacturing to gather facts and reach scientifically sound conclusions. - Prepare clear, concise, and comprehensive investigation reports aligned with FDA and cGMP standards. - Develop and document corrective/preventive actions (CAPAs), change controls, and impact assessments. - Review quality records for accuracy, completeness, and timely completion, supporting internal/external audits and regulatory inspections. - Identify and recommend process improvements to enhance laboratory compliance and reduce repeat events. Required Skills and Experience - Bachelor's in Chemistry, Microbiology, Biology, Biochemistry, Pharmaceutical Sciences, or related discipline. - 2+ years' experience in GMP-regulated pharmaceutical, biotech, or biologics environment. - 1+ year direct experience authoring and leading QC laboratory investigations. - Advanced technical writing and documentation skills. - Strong knowledge of FDA regulations, cGMP requirements, and laboratory investigation best practices. - Demonstrated expertise in root cause analysis, analytical problem solving, and scientific evaluation of laboratory data. Preferred Skills - Experience with electronic Quality Management Systems (e.g., TrackWise). - Familiarity with FDA OOS Guidance and current Good Manufacturing Practice regulations. - Experience reviewing analytical chemistry and/or microbiological testing data. Benefits - Exposure to high-impact, cross-functional projects in a leading GMP environment. - Opportunity to work alongside industry experts and further develop technical writing and investigation leadership skills. - Gain hands-on experience supporting regulatory inspections and audits. - Supportive culture focused on continuous improvement and professional growth. How to Apply Take the next step in your quality and compliance career! Submit your resume detailing relevant technical writing and QC investigation experience.
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About Indotronix

Sourced by ZipRecruiter

In 1986, Indotronix established itself in the staffing space. 22 years later, Avani entered the scene, offering consulting and technology development. Finally, in 2016, the two joined forces to begin delivering talent across all areas, from Staffing to Consulting to unique platform development.

Industry

Recruiting and staffing services

Company size

1,001 - 5,000 Employees

Headquarters location

Rochester, NY, US

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