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Full Time Biotech Technical Writer Jobs (NOW HIRING)

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Technical Writer

Springfield, NJ

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 ...

ASI Systems Engineering

GMP Technical Writer

Kenosha, WI · On-site

$60 - $75/hr

... biotech, or medical device manufacturing • Demonstrated experience authoring Deviation reports, CAPA records, and Change Control packages • Proficiency with electronic quality management systems ...

Linchpin Solutions Inc

Technical Writer

Quantico, VA · On-site

Fulltime, On-site, Quantico, VA; limited travel as required ( Role Overview: The Technical Writer supports the MOCTT Documentation Support Services mission at the Marine Corps Tactics and Operations ...

Linchpin Solutions Inc

Technical Writer

Quantico, VA · On-site

Fulltime, On-site, Quantico, VA; limited travel as required ( Role Overview: The Technical Writer supports the MOCTT Documentation Support Services mission at the Marine Corps Tactics and Operations ...

Pivotal Point LLC

Technical Writer

Falls Church, VA · On-site +1

Job Type Full-time Description Job Title: Technical Writer - Customer Experience Support (Platform One) Location: Remote Clearance Level: Secret Required Employment Type: Full Time Start Date:

Aquila Technology

Technical Writer

Lexington, MA

Technical Writer Clearance Level: Must be a US Citizen and eligible to obtain an Secret Clearance ... Full-time employment Tuition & Training Reimbursement - 5K annually for pre-approved, Eligible ...

NuAxis Innovations

Technical Writer

Arlington, VA · On-site

We are currently seeking a talented and motivated Technical Writer for a Full-Time position. Essential Functions: Responsible for designing/creating/maintaining technical and knowledge-based ...

ENTEK International

Technical Writer

Henderson, NV · On-site

$30 - $33/hr

Job Type Full-time Description Join ENTEK in Henderson, Nevada ENTEK is excited to welcome a Technical Writer to our team in Henderson, Nevada. If you're passionate about creating clear, engaging ...

Amatriot Group, LLC

Technical Writer

Crane, IN · On-site

$100K - $120K/yr

Crane, IN Job Type: Full-Time Target Salary Range*: $100,000 - $120,000. *This represents the ... For this Technical Writer position, you will be responsible for producing, proof-reading, editing ...

Gromelski & Associates

Technical Writer

Manassas, VA · On-site

$90K - $120K/yr

Technical Writer Gromelski and Associates, Inc. (GAI) partners with prime contractors to provide ... Job: Full Time Employee, 40 hours/week, onsite Start Date: Immediate Salary Range: $90,000 - $120 ...

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Full Time Biotech Technical Writer information

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$66

How much do full time biotech technical writer jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for full time 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 Full Time Biotech Technical Writer vs Full Time Medical Writer?

AspectFull Time Biotech Technical WriterFull Time Medical Writer
CredentialsBachelor's degree in life sciences, writing experienceAdvanced degree (MD, PhD), medical/scientific background
Work EnvironmentBiotech companies, research labs, CROsPharmaceutical companies, medical communications firms
Industry UsageDevelops technical documentation for biotech productsCreates clinical, regulatory, and medical education content

Full Time Biotech Technical Writers focus on creating technical documents related to biotech products, often with a background in life sciences. Full Time Medical Writers typically have advanced medical or scientific degrees and produce clinical and regulatory content for the medical and pharmaceutical industries. While both roles require strong writing skills, their focus areas and required credentials differ significantly.

What cities are hiring for Full Time Biotech Technical Writer jobs? Cities with the most Full Time 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 Full Time Biotech Technical Writer jobs? States with the most job openings for Full Time Biotech Technical Writer jobs include:
Full Time Biotech Technical Writer jobs near you
Technical Writer

Technical Writer

Indotronix International Corporation

High Point, NC • On-site

$20 - $27/hr

Full-time

Posted 19 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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