Minimum 2 years of experience in technical writing for Regulatory CMC documentation within the pharmaceutical or biotechnology industry. * Familiarity with eCTD structure for regulatory submissions.
Minimum 2 years of experience in technical writing for Regulatory CMC documentation within the pharmaceutical or biotechnology industry. * Familiarity with eCTD structure for regulatory submissions.
Minimum 2 years of experience in technical writing for Regulatory CMC documentation within the pharmaceutical or biotechnology industry. * Familiarity with eCTD structure for regulatory submissions.
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Minimum 2 years of experience in technical writing for Regulatory CMC documentation within the pharmaceutical or biotechnology industry. * Familiarity with eCTD structure for regulatory submissions.
Job ID: 21-12907 Skills: -Ability to write technical documents, and tenacious attention to detail ... in the biotech or pharmaceutical manufacturing industry is beneficial. -Proficiency in a broad ...
Job ID: 21-12907 Skills: -Ability to write technical documents, and tenacious attention to detail ... in the biotech or pharmaceutical manufacturing industry is beneficial. -Proficiency in a broad ...
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 ...
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 ...
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 ...
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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 ...
Working knowledge of GMP / Biotechnology manufacturing background referred, some experience in QA and/or Documentation creation preferred. Ability to manage multiple priorities. * Technical writing ...
Working knowledge of GMP / Biotechnology manufacturing background referred, some experience in QA and/or Documentation creation preferred. Ability to manage multiple priorities. * Technical writing ...
Working knowledge of GMP / Biotechnology manufacturing background referred, some experience in QA and/or Documentation creation preferred. Ability to manage multiple priorities. * Technical writing ...
New
Working knowledge of GMP / Biotechnology manufacturing background referred, some experience in QA and/or Documentation creation preferred. Ability to manage multiple priorities. * Technical writing ...
New
Technical Writer II
Swiftwater, PA · On-site
Job Summary : eTeam is seeking a Technical Writer II to support the implementation of the OneLIMS ... biotech environments (e.g., Veeva) preferred • Proficiency in PowerPoint with the ability to ...
Technical Writer II
Swiftwater, PA · On-site
Job Summary : eTeam is seeking a Technical Writer II to support the implementation of the OneLIMS ... biotech environments (e.g., Veeva) preferred • Proficiency in PowerPoint with the ability to ...
Near New Brunswick, NJ Join a leading Contract Development and Manufacturing Organization (CDMO) supporting the pharmaceutical and biotechnology industries! Position Summary As a Technical Writer ...
Near New Brunswick, NJ Join a leading Contract Development and Manufacturing Organization (CDMO) supporting the pharmaceutical and biotechnology industries! Position Summary As a Technical Writer ...
Required : • 3+ years of technical writing experience in a GxP-regulated pharmaceutical, biotech, or medical device environment • Proven experience authoring IQ/OQ/PQ protocols, SOPs, and RTMs in ...
New
Required : • 3+ years of technical writing experience in a GxP-regulated pharmaceutical, biotech, or medical device environment • Proven experience authoring IQ/OQ/PQ protocols, SOPs, and RTMs in ...
New
This freelance opportunity is remote and hours are flexible, so you can work whenever is best for ... Professional writing experience (copywriter, journalist, technical writer, editor, etc.
This freelance opportunity is remote and hours are flexible, so you can work whenever is best for ... Professional writing experience (copywriter, journalist, technical writer, editor, etc.
Technical Writer- LabVantage
Indianapolis, IN · On-site +1
Generate AI-accelerated draft documentation and testing outputs Required Qualifications: * 5+ years of technical writing experience in GMP-regulated pharma or biotech environments * Hands-on ...
Technical Writer- LabVantage
Indianapolis, IN · On-site +1
Generate AI-accelerated draft documentation and testing outputs Required Qualifications: * 5+ years of technical writing experience in GMP-regulated pharma or biotech environments * Hands-on ...
... biotech environments (e.g., Veeva, GMP) Description The OneLIMS EM project technical writer is responsible for supporting on-time implementation of OneLIMS EM global system for the Swiftwater, PA ...
New
... biotech environments (e.g., Veeva, GMP) Description The OneLIMS EM project technical writer is responsible for supporting on-time implementation of OneLIMS EM global system for the Swiftwater, PA ...
New
... biotech acceptable). * 3+ years of people leadership experience, including managing writers ... Prior leadership of technical writing teams within a medical device organization. * Extensive ...
... biotech acceptable). * 3+ years of people leadership experience, including managing writers ... Prior leadership of technical writing teams within a medical device organization. * Extensive ...
... biotech acceptable). * 3+ years of people leadership experience, including managing writers ... Prior leadership of technical writing teams within a medical device organization. * Extensive ...
... biotech acceptable). * 3+ years of people leadership experience, including managing writers ... Prior leadership of technical writing teams within a medical device organization. * Extensive ...
... biotech acceptable). * 3+ years of people leadership experience, including managing writers ... Prior leadership of technical writing teams within a medical device organization. * Extensive ...
... biotech acceptable). * 3+ years of people leadership experience, including managing writers ... Prior leadership of technical writing teams within a medical device organization. * Extensive ...
... biotech acceptable). * 3+ years of people leadership experience, including managing writers ... Prior leadership of technical writing teams within a medical device organization. * Extensive ...
... biotech acceptable). * 3+ years of people leadership experience, including managing writers ... Prior leadership of technical writing teams within a medical device organization. * Extensive ...
The Technical Writer will interact with individuals at multiple levels within all functional ... Biotechnology, Pharmaceuticals or another Regulated Industry.Experience in Quality Assurance ...
The Technical Writer will interact with individuals at multiple levels within all functional ... Biotechnology, Pharmaceuticals or another Regulated Industry.Experience in Quality Assurance ...
Freelance Biotech Technical Writer information
See salary details
$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
How much do freelance biotech technical writer jobs pay per hour?
As of Jun 12, 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?
| 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.
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Contractor
Medical, Retirement
Posted 15 hours ago
Job description
SOKOL GxP Services seeking a Technical Writer and Document Specialist to support CMC documentation for a late-stage clinical cell therapy program. This role will sit within the Cell Therapy Development Project and Portfolio Management Office and will support regulatory submission activities, dossier preparation, and cross-functional document coordination.
The Technical Writer will author and co-author scientific content for CTD Quality sections aligned with regulatory strategy for clinical and life-cycle CMC submissions. This includes supporting Module 2.3 and Module 3 content, coordinating source documentation, managing submission timelines, reviewing and adjudicating comments, facilitating data verification, and helping ensure consistency and clarity across the dossier.
This position requires close collaboration with Process Development, Analytical Development, Cell Therapy Technical Operations, Quality, Regulatory Sciences, CMC matrix team leaders, project management, document management, and external suppliers as needed. The ideal candidate will be detail-oriented, organized, deadline-driven, and comfortable working in a fast-paced regulatory submission environment.
This is a 12-month hybrid contract position based in New Brunswick, NJ, with 50% onsite presence required and occasional travel to other local New Jersey sites for larger team meetings.
Requirements
Required Qualifications:
- Bachelor's degree required; Biology or related discipline preferred.
- Minimum 2 years of experience in technical writing for Regulatory CMC documentation within the pharmaceutical or biotechnology industry.
- Familiarity with eCTD structure for regulatory submissions.
- Experience supporting CMC regulatory documentation, dossier creation, and submission timelines.
- Cell therapy CMC experience required.
- Familiarity with CTD Quality sections, including Module 2.3 and Module 3.
- Understanding of source documentation requirements for regulatory submissions and how source documents connect to the authoring process.
- Strong verbal and written communication skills.
- Strong attention to detail, planning, organizational, and negotiating skills.
- Demonstrated ability to deliver high-quality documentation within filing deadlines.
- Proficiency with Microsoft Office applications, including Word, Excel, SharePoint, and PowerPoint.
- Ability to work independently under supervision and collaborate cross-functionally with scientific, regulatory, project management, and document management teams.
- Ability to work in a fast-paced, changing team environment and prioritize multiple tasks.
Preferred Qualifications:
- BLA regulatory submission experience strongly preferred.
- Experience with computer-assisted document preparation tools preferred.
- Proficiency in compliance-ready standards for final publication preferred.
- Experience in biotech/pharma end-to-end product development preferred.
- Experience training others on procedures, systems access, and document management best practices preferred.
Benefits
Competitive hourly rate, $: 33.03 - 41.95 (W-2, no C2C option)
Working hours: Monday to Friday, regular business hours
Hybrid position: 50% onsite required
Location: New Brunswick, NJ
12-month contract with possibility of extension
Occasional travel to other local New Jersey sites for larger team meetings, approximately 2-3 times per year
Health insurance, holiday pay, 401(k), referral bonus program