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Freelance Biotech Technical Writer Jobs (NOW HIRING)

GMP Technical Writer

Madison, WI · On-site

$50 - $70/hr

Requirements Required Qualifications & Experience * 4+ years of GMP technical writing experiencewithin pharmaceutical, biotechnology, medical device, or other regulatedmanufacturing environments.

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 ...

Minimum of 3 years of technical writing experience, preferably within a regulated GMP environment, and ideally in pharmaceutical, biopharmaceutical, or biotechnology industries. Additional ...

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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 Sep 14, 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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Infographic showing various Freelance Biotech Technical Writer job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 86% Full Time, 9% Part Time, 2% Contract, and 1% Nights. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $48,412 per year, or $23.3 per hour.
Edwards Lifesciences Corporation
Medical Equipment and Supplies Manufacturing • 10K+ employees

$68K - $96K/yr

Full-time

Re-posted 13 days ago


Edwards Lifesciences rating

8.2

Company rating: 8.2 out of 10

Based on 31 frontline employees who took The Breakroom Quiz


Job description

Many structural heart patients suffer from heart failure with limited options. Our Implantable Heart Failure Management (IHFM) team, part of the AI, Product and Platforms organization, is at the forefront of addressing these unmet patient needs through pioneering technology that enables early, targeted therapeutic intervention. Our innovative solutions are not just transforming patient care but also creating a unique and exciting environment for our team members. It is our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.

At Edwards Lifesciences, the IHFM AI, Product and Platforms organization designs and builds the software and data products that clinicians and patients depend on. As a Technical Writer, you own well-scoped controlled documentation that keeps our regulated software traceable and audit ready. You produce and maintain design control artifacts and user-facing documentation with limited guidance, partnering with engineering, quality, and product.

Based in Irvine, CA, you'll join a high-impact medtech innovation hub in the heart of Orange County, collaborating in person with cross-functional teams to shape patient-focused technology.

How You'll Make an Impact
  • Create and maintain moderately complex Good Manufacturing Practices (GMP) protocols, reports, technical summaries, and test procedures.

  • Develop well-scoped controlled documentation that supports regulated software traceability and audit readiness.

  • Maintain documentation in a standard format and follow established guidelines for content quality, organization, and consistency.

  • Partner with production employees, technicians, engineers, project teams, regulatory partners, and management to understand product, component, or device changes.

  • Review documents for style, clarity, grammar, punctuation, and overall usability.

  • Identify and resolve inconsistencies in content, structure, or document development, and work with authors to recommend appropriate updates.

  • Respond to requests for clarification or explanation of reference materials and technical documentation.

  • Support additional documentation-related needs as assigned by leadership.

What you'll need (Required):
  • Bachelor's degree in a related field and 3 years of technical writing experience, or equivalent work experience based on Edwards criteria.

  • This is an onsite role based in Irvine, CA. Relocation assistance is not provided, and candidates must reside within a 50-mile radius of Irvine to be considered.

What else we look for (Preferred):
  • Biotechnology, medical device, or regulated industry experience, or equivalent work experience based on Edwards criteria.

  • Experience creating or maintaining documentation types such as procedures, routers, process sheets, technical summaries, protocols, and test reports.

  • Solid understanding of policies, procedures, and guidelines relevant to technical documentation development.

  • Strong editing, proofreading, and technical writing skills, with careful attention to style, clarity, grammar, and punctuation.

  • Proficiency with Microsoft Office Suite, including Word, Excel, PowerPoint, and Publisher; Adobe and Photoshop experience preferred.

  • Good written and verbal communication skills in English, with strong interpersonal skills.

  • Good problem-solving, critical thinking, organization, and prioritization skills in a fast-paced environment.

  • Ability to work independently on more complex projects or lines of work, with work reviewed for accuracy and soundness.

  • Ability to collaborate across interdepartmental teams, build productive internal and external working relationships, and represent the organization on specific projects.

  • Strict attention to detail and commitment to following all company rules and requirements, including Environmental Health & Safety expectations and applicable protocols.

Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California (CA), the base pay range for this position is $68,000 to $96,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.


Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.


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About Edwards Lifesciences

Sourced by ZipRecruiter

Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide. For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Irvine, CA, US

Year founded

1958