Belmont, MA · On-site
$50 - $75/hr
Custom Learning Designs has partnered with Hueman to find a Technical Writer - Freelance, remote ... Pharmaceutical, biotech, medical device sales training experience a plus * At Custom Learning ...
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Belmont, MA · On-site
$50 - $75/hr
Custom Learning Designs has partnered with Hueman to find a Technical Writer - Freelance, remote ... Pharmaceutical, biotech, medical device sales training experience a plus * At Custom Learning ...
New
Swiftwater, PA · On-site
Pharmaceutical / Biotech Manufacturing Position Overview We are seeking a Technical Writer to support the implementation of a new digital platform by developing, updating, and converting technical ...
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Swiftwater, PA · On-site
Pharmaceutical / Biotech Manufacturing Position Overview We are seeking a Technical Writer to support the implementation of a new digital platform by developing, updating, and converting technical ...
New
Prior experience in biotechnology area/ cell therapy area preferred good oral and written ... With Regards, Shiva Kapoor Technical Recruiter Direct: 732-429-1929
Prior experience in biotechnology area/ cell therapy area preferred good oral and written ... With Regards, Shiva Kapoor Technical Recruiter Direct: 732-429-1929
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 ...
I want a senior level persons who can self Manage and motivate and some biology, life science, pharma, biotech or cro experience. Sr Technical Writer/Lead to assist with writing requirements, FS ...
I want a senior level persons who can self Manage and motivate and some biology, life science, pharma, biotech or cro experience. Sr Technical Writer/Lead to assist with writing requirements, FS ...
Barceloneta, PR · On-site
Position Overview We are seeking experienced Technical Writers / Manufacturing SOP Specialists to support a major initiative within a Biotech Drug Substance Manufacturing Operation in Barceloneta ...
Barceloneta, PR · On-site
Position Overview We are seeking experienced Technical Writers / Manufacturing SOP Specialists to support a major initiative within a Biotech Drug Substance Manufacturing Operation in Barceloneta ...
Andover, MA · On-site
... biotech production or R&D experience, and/or pharmaceutical regulatory submission writing ... Authoring of technical protocols, reports, memorandum, records, and related correspondence Retrieve ...
Andover, MA · On-site
... biotech production or R&D experience, and/or pharmaceutical regulatory submission writing ... Authoring of technical protocols, reports, memorandum, records, and related correspondence Retrieve ...
We are looking for a freelance/contractor Technical Writer to produce high-quality documentation. Responsibilities: Work with internal teams to obtain an in-depth understanding of the product and the ...
We are looking for a freelance/contractor Technical Writer to produce high-quality documentation. Responsibilities: Work with internal teams to obtain an in-depth understanding of the product and the ...
Support documentation activities related to fill/finish manufacturing processes Qualifications: * 5-8 years of Technical Writing experience within the pharmaceutical or biotech industry * Strong ...
Support documentation activities related to fill/finish manufacturing processes Qualifications: * 5-8 years of Technical Writing experience within the pharmaceutical or biotech industry * Strong ...
... or biotech environments (e.g., Veeva) preferred Proficiency in PowerPoint with the ability to ... technical writer is responsible for supporting on-time implementation of OneLIMS EM global system ...
New
... or biotech environments (e.g., Veeva) preferred Proficiency in PowerPoint with the ability to ... technical writer is responsible for supporting on-time implementation of OneLIMS EM global system ...
New
The Technical Document Writer will be responsible for producing high-quality cGMP documentation ... Prior experience working in a biotech/pharmaceutical company. Exceptional written/verbal ...
The Technical Document Writer will be responsible for producing high-quality cGMP documentation ... Prior experience working in a biotech/pharmaceutical company. Exceptional written/verbal ...
... biotechnology or pharmaceutical industry Direct experience in GXP-compliant quality systems is ... Excellent communication skills including: technical writing, interpersonal and collaborative skills;
... biotechnology or pharmaceutical industry Direct experience in GXP-compliant quality systems is ... Excellent communication skills including: technical writing, interpersonal and collaborative skills;
Kenosha, WI · On-site
... biotech, or medical device manufacturing • Demonstrated experience authoring Deviation reports, CAPA records, and Change Control packages • Proficiency with electronic quality management systems ...
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Kenosha, WI · On-site
... biotech, or medical device manufacturing • Demonstrated experience authoring Deviation reports, CAPA records, and Change Control packages • Proficiency with electronic quality management systems ...
New
Qualifications Required Skills and Experience * 5 to 8 years technical writing experience in a hardware, software, biotechnology, or medical environment, including documentation for a highly ...
Qualifications Required Skills and Experience * 5 to 8 years technical writing experience in a hardware, software, biotechnology, or medical environment, including documentation for a highly ...
Qualifications Required Skills and Experience * 5 to 8 years technical writing experience in a hardware, software, biotechnology, or medical environment, including documentation for a highly ...
Qualifications Required Skills and Experience * 5 to 8 years technical writing experience in a hardware, software, biotechnology, or medical environment, including documentation for a highly ...
Sunnyvale, CA · On-site
Qualifications Required Skills and Experience * 5 to 8 years technical writing experience in a hardware, software, biotechnology, or medical environment, including documentation for a highly ...
Sunnyvale, CA · On-site
Qualifications Required Skills and Experience * 5 to 8 years technical writing experience in a hardware, software, biotechnology, or medical environment, including documentation for a highly ...
Technical Writing ... Pharmaceutical/Biotech Industry Experience * Quality Systems (eQMS, EDMS) * Cross-Functional ...
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Technical Writing ... Pharmaceutical/Biotech Industry Experience * Quality Systems (eQMS, EDMS) * Cross-Functional ...
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Demonstrates strong verbal, written, and interpersonal communication skills. Demonstrates ... Previous experience in Pharmaceutical or Biotechnology industry, preferably in Quality Control.
Demonstrates strong verbal, written, and interpersonal communication skills. Demonstrates ... Previous experience in Pharmaceutical or Biotechnology industry, preferably in Quality Control.
Ridgefield, CT · On-site
$54 - $55.70/hr
Required • Significant working experience (>6 years) in pharmaceutical/biotech CMC and analytical ... technical writing skills • High attention to detail and scientific rigor • Effective ...
Ridgefield, CT · On-site
$54 - $55.70/hr
Required • Significant working experience (>6 years) in pharmaceutical/biotech CMC and analytical ... technical writing skills • High attention to detail and scientific rigor • Effective ...
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.
$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.
$50 - $75/hr
Contractor
Posted 2 days ago
Custom Learning Designs has partnered with Hueman to find a Technical Writer - Freelance, remote.
Custom Learning Designs (CLD) is a leading provider of custom training solutions for pharmaceutical and life sciences companies. At CLD, we support our customers in developing customized training for their commercial sales teams, medical teams (MSLs), patients, and physicians.
Freelance Medical Writer
We are seeking an experienced Freelance Medical Writer to join our team and develop high-quality, scientifically accurate content across a range of medical and pharmaceutical communications. The ideal candidate is a strong writer with a solid foundation in the life sciences who can translate complex clinical and scientific information into clear, compelling, and accessible prose for a variety of audiences. This role requires the ability to independently research primary literature, apply sound analytical judgment, and synthesize findings into well-organized, detail-oriented deliverables under tight deadlines. The successful candidate will bring both precision and creativity to their work, along with the ability to quickly understand new medical topics in depth and communicate them effectively.
Requirements
Qualifications
At Custom Learning Designs, you'll work with top pharma companies, contribute to impactful training solutions, and grow in a collaborative and innovative environment. Apply now to be part of a mission-driven team shaping the future of pharma training.
Hueman is proud to partner with Custom Learning Designs as the exclusive recruitment partner for this role. If you are interested in learning more about a career with CLD as a Freelance Writer apply today!
