Technical Writer
$68K - $96K/yr
As a Technical Writer, you own well-scoped controlled documentation that keeps our regulated ... Biotechnology, medical device, or regulated industry experience, or equivalent work experience ...
$68K - $96K/yr
As a Technical Writer, you own well-scoped controlled documentation that keeps our regulated ... Biotechnology, medical device, or regulated industry experience, or equivalent work experience ...
$68K - $96K/yr
As a Technical Writer, you own well-scoped controlled documentation that keeps our regulated ... Biotechnology, medical device, or regulated industry experience, or equivalent work experience ...
Irvine, CA · On-site
$68K - $96K/yr
As a Technical Writer, you own well-scoped controlled documentation that keeps our regulated ... Biotechnology, medical device, or regulated industry experience, or equivalent work experience ...
Irvine, CA · On-site
$68K - $96K/yr
As a Technical Writer, you own well-scoped controlled documentation that keeps our regulated ... Biotechnology, medical device, or regulated industry experience, or equivalent work experience ...
Technical Writer Location: Santa Clara CA 95054 Duration: 06+ months (Possibilities of extension ... Freelance, Power Point, Visio), and or other equivalent tools. Experience in SDLC, analysis, design ...
Technical Writer Location: Santa Clara CA 95054 Duration: 06+ months (Possibilities of extension ... Freelance, Power Point, Visio), and or other equivalent tools. Experience in SDLC, analysis, design ...
San Dimas, CA · On-site
Demonstrates strong verbal, written, and interpersonal communication skills. Demonstrates ... Previous experience in Pharmaceutical or Biotechnology industry, preferably in Quality Control.
San Dimas, CA · On-site
Demonstrates strong verbal, written, and interpersonal communication skills. Demonstrates ... Previous experience in Pharmaceutical or Biotechnology industry, preferably in Quality Control.
Prior experience as a Technical Writer in pharma, biotech, medical device, or another regulated industry. * Strong understanding of GMP/GxP documentation practices. * Excellent writing, editing, and ...
Prior experience as a Technical Writer in pharma, biotech, medical device, or another regulated industry. * Strong understanding of GMP/GxP documentation practices. * Excellent writing, editing, and ...
... the biotech or pharmaceutical manufacturing industry is beneficial. • Proficiency in a broad range of technical skills, including expert-level use of Google Software, MS Excel, Word, PowerPoint ...
... the biotech or pharmaceutical manufacturing industry is beneficial. • Proficiency in a broad range of technical skills, including expert-level use of Google Software, MS Excel, Word, PowerPoint ...
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.
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.
Senior level 8-15 years of experience in technical writing within the Pharma, Medical Device, or BioTech industries is desired. Desired Aptitude and Skill Set: * Resourceful * Extremely detail ...
Senior level 8-15 years of experience in technical writing within the Pharma, Medical Device, or BioTech industries is desired. Desired Aptitude and Skill Set: * Resourceful * Extremely detail ...
Senior level 8-15 years of experience in technical writing within the Pharma, Medical Device, or BioTech industries is desired. Desired Aptitude and Skill Set: * Resourceful * Extremely detail ...
Senior level 8-15 years of experience in technical writing within the Pharma, Medical Device, or BioTech industries is desired. Desired Aptitude and Skill Set: * Resourceful * Extremely detail ...
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 ...
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 ...
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 ...
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 ...
Fishers, IN · On-site
Minimum of 3 years of technical writing experience, preferably within a regulated GMP environment, and ideally in pharmaceutical, biopharmaceutical, or biotechnology industries. Additional ...
Fishers, IN · On-site
Minimum of 3 years of technical writing experience, preferably within a regulated GMP environment, and ideally in pharmaceutical, biopharmaceutical, or biotechnology industries. Additional ...
Hands-on technical writing experience in a pharmaceutical, biotech, or regulated GMP manufacturing environment. * Direct experience authoring validation and qualification documentation. * Experience ...
Quick apply
Hands-on technical writing experience in a pharmaceutical, biotech, or regulated GMP manufacturing environment. * Direct experience authoring validation and qualification documentation. * Experience ...
Cranbury, NJ · On-site
$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 ...
Quick apply
Cranbury, NJ · On-site
$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 ...
Technical Writer SwiftWater, PA - Onsite 9+ Months Role will work with a team on a new digital ... or biotech environment) * Must possess sound interpersonal and information gathering skills, be ...
Quick apply
Technical Writer SwiftWater, PA - Onsite 9+ Months Role will work with a team on a new digital ... or biotech environment) * Must possess sound interpersonal and information gathering skills, be ...
Fishers, IN · On-site
Minimum of 3 years of technical writing experience, preferably within a regulated GMP environment, and ideally in pharmaceutical, biopharmaceutical, or biotechnology industries. Additional ...
Fishers, IN · On-site
Minimum of 3 years of technical writing experience, preferably within a regulated GMP environment, and ideally in pharmaceutical, biopharmaceutical, or biotechnology industries. Additional ...
Minimum of 3 years of technical writing experience, preferably within a regulated GMP environment, and ideally in pharmaceutical, biopharmaceutical, or biotechnology industries. Additional ...
Minimum of 3 years of technical writing experience, preferably within a regulated GMP environment, and ideally in pharmaceutical, biopharmaceutical, or biotechnology industries. Additional ...
Fishers, IN · On-site
Minimum of 3 years of technical writing experience, preferably within a regulated GMP environment, and ideally in pharmaceutical, biopharmaceutical, or biotechnology industries. Additional ...
Quick apply
Fishers, IN · On-site
Minimum of 3 years of technical writing experience, preferably within a regulated GMP environment, and ideally in pharmaceutical, biopharmaceutical, or biotechnology industries. Additional ...
Fishers, IN · On-site
Minimum of 3 years of technical writing experience, preferably within a regulated GMP environment, and ideally in pharmaceutical, biopharmaceutical, or biotechnology industries. Additional ...
Fishers, IN · On-site
Minimum of 3 years of technical writing experience, preferably within a regulated GMP environment, and ideally in pharmaceutical, biopharmaceutical, or biotechnology industries. Additional ...
... biotechnology industries. Additional Preferences: Proficient in writing clear, concise, and accurate technical documentation. Strong understanding of GMP manufacturing processes and regulatory ...
... biotechnology industries. Additional Preferences: Proficient in writing clear, concise, and accurate technical documentation. Strong understanding of GMP manufacturing processes and regulatory ...
$7.45 - $9.77
5% of jobs
$9.77 - $12.08
0% of jobs
$12.08 - $14.40
1% of jobs
$14.40 - $16.72
2% of jobs
$16.72 - $19.03
3% of jobs
$20.35 is the 25th percentile. Wages below this are outliers.
$19.03 - $21.35
23% of jobs
The median wage is $22.51 / hr.
$21.35 - $23.67
30% of jobs
$25.24 is the 75th percentile. Wages above this are outliers.
$23.67 - $25.98
15% of jobs
$25.98 - $28.30
6% of jobs
$28.30 - $30.62
6% of jobs
$30.62 - $32.93
7% of jobs
$7
$23
$32
| Aspect | Freelance Biotech Technical Writer | Freelance Medical Writer |
|---|---|---|
| Credentials | Scientific background, life sciences degree | Medical or health sciences degree, clinical knowledge |
| Work Environment | Biotech companies, research labs, contract agencies | Pharmaceutical firms, healthcare organizations, clinical research |
| Industry Usage | Biotech, research, and development sectors | Pharmaceuticals, clinical trials, healthcare communication |
| Common Search/Comparison | Yes | Yes |
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.
Cities with the most Freelance Biotech Technical Writer job openings:
The most popular types of Biotech Technical Writer jobs are:
States with the most job openings for Freelance Biotech Technical Writer jobs include:
For Freelance Biotech Technical Writer jobs, the most frequently searched job titles are:

Irvine, CA
$68K - $96K/yr
Full-time
Re-posted 13 days ago
8.2
Based on 31 frontline employees who took The Breakroom Quiz
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 ImpactCreate 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.
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.
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.
Get the full story on Breakroom
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.
Medical equipment and supplies manufacturing
10,000+ Employees
Irvine, CA, US
1958