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 ...
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 ...
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 ...
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 ...
Technical Writer
Portola, CA · On-site
Coordinates with Manager, Technical Publications to support team objectives. * Provides input for ... TRAVEL REQUIREMENTS Ability to travel up to 5% of the time, including overnight and weekend travel.
Technical Writer
Portola, CA · On-site
Coordinates with Manager, Technical Publications to support team objectives. * Provides input for ... TRAVEL REQUIREMENTS Ability to travel up to 5% of the time, including overnight and weekend travel.
Technical Writer - Operations
$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 ...
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Technical Writer - Operations
$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 ...
GMP Technical Writer / SQA Specialist
Tampa, FL · On-site
$60 - $70/hr
Support inspection-readiness anddocumentation-remediation initiatives Requirements Requirements Required Qualifications * 3-6+ years of GMP technical writing experience inpharmaceutical, biotech, or ...
GMP Technical Writer / SQA Specialist
Tampa, FL · On-site
$60 - $70/hr
Support inspection-readiness anddocumentation-remediation initiatives Requirements Requirements Required Qualifications * 3-6+ years of GMP technical writing experience inpharmaceutical, biotech, or ...
Minimum of 3 years of experience in technical writing within a regulated GMP environment, preferably in the pharmaceutical, biopharmaceutical, or biotechnology industries. Additional Preferences:
Minimum of 3 years of experience in technical writing within a regulated GMP environment, preferably in the pharmaceutical, biopharmaceutical, or biotechnology industries. Additional Preferences:
... or biotechnology industries. Additional Preferences: · Proficient in writing clear, concise, and accurate technical documentation. · Strong understanding of GMP manufacturing processes and ...
... or biotechnology industries. Additional Preferences: · Proficient in writing clear, concise, and accurate technical documentation. · Strong understanding of GMP manufacturing processes and ...
Engineering Technical Writer
Fishers, IN · On-site
... biotechnology industries. Additional Preferences: • Proficient in writing clear, concise, and accurate technical documentation. • Strong understanding of GMP manufacturing processes and ...
Engineering Technical Writer
Fishers, IN · On-site
... biotechnology industries. Additional Preferences: • Proficient in writing clear, concise, and accurate technical documentation. • Strong understanding of GMP manufacturing processes and ...
... or biotechnology industries. Additional Preferences: · Proficient in writing clear, concise, and accurate technical documentation. · Strong understanding of GMP manufacturing processes and ...
Quick apply
... or biotechnology industries. Additional Preferences: · Proficient in writing clear, concise, and accurate technical documentation. · Strong understanding of GMP manufacturing processes and ...
Description We are seeking a Technical Writer to support GMP documentation activities in a biotech environment. This role will focus on creating, editing, and maintaining compliant documentation ...
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Description We are seeking a Technical Writer to support GMP documentation activities in a biotech environment. This role will focus on creating, editing, and maintaining compliant documentation ...
Contract Technical Writer
$40 - $47/hr
... biotech, medical device, or similar manufacturing environment. * Experience authoring and revising SOPs, batch records, work instructions, and laboratory documentation. * Working knowledge of CAPA ...
New
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Contract Technical Writer
$40 - $47/hr
... biotech, medical device, or similar manufacturing environment. * Experience authoring and revising SOPs, batch records, work instructions, and laboratory documentation. * Working knowledge of CAPA ...
New
Contract Technical Writer
$40 - $47/hr
... biotech, medical device, or similar manufacturing environment. * Experience authoring and revising SOPs, batch records, work instructions, and laboratory documentation. * Working knowledge of CAPA ...
New
Contract Technical Writer
$40 - $47/hr
... biotech, medical device, or similar manufacturing environment. * Experience authoring and revising SOPs, batch records, work instructions, and laboratory documentation. * Working knowledge of CAPA ...
New
... Technical Writer to join our team. If you want an exciting career where you use your previous ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
... Technical Writer to join our team. If you want an exciting career where you use your previous ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
... Technical Writer to join our team. If you want an exciting career where you use your previous ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
... Technical Writer to join our team. If you want an exciting career where you use your previous ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
The Technical Writer will work closely with the MSAT engineers and other cross-functional teams to ... Biotechnology, Engineering). A bachelor's degree is preferred. • Minimum of 0 - 3 years of ...
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The Technical Writer will work closely with the MSAT engineers and other cross-functional teams to ... Biotechnology, Engineering). A bachelor's degree is preferred. • Minimum of 0 - 3 years of ...
The Technical Writer will work closely with the MSAT engineers and other cross-functional teams to ... Biotechnology, Engineering). A bachelor's degree is preferred. • Minimum of 0 - 3 years of ...
The Technical Writer will work closely with the MSAT engineers and other cross-functional teams to ... Biotechnology, Engineering). A bachelor's degree is preferred. • Minimum of 0 - 3 years of ...
Minimum of 0 - 3 years of experience in technical writing within a GMP environment, preferably in the pharmaceutical, biopharmaceutical, or biotechnology industries. Additional Preferences:
Minimum of 0 - 3 years of experience in technical writing within a GMP environment, preferably in the pharmaceutical, biopharmaceutical, or biotechnology industries. Additional Preferences:
Technical Writer in Mountain View, CA 94043
Mountain View, CA · On-site
$60 - $65/hr
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 audience.
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Technical Writer in Mountain View, CA 94043
Mountain View, CA · On-site
$60 - $65/hr
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 audience.
Overnight Biotech Technical Writer information
See salary details
$13.70 - $18.47
2% of jobs
$18.47 - $23.23
7% of jobs
$23.23 - $27.99
12% of jobs
$29.11 is the 25th percentile. Wages below this are outliers.
$27.99 - $32.76
16% of jobs
The median wage is $36.33 / hr.
$32.76 - $37.52
17% of jobs
$37.52 - $42.29
14% of jobs
$45.38 is the 75th percentile. Wages above this are outliers.
$42.29 - $47.05
11% of jobs
$47.05 - $51.81
10% of jobs
$51.81 - $56.58
5% of jobs
$56.58 - $61.34
3% of jobs
$61.34 - $66.11
3% of jobs
$13
$38
$66
How much do overnight biotech technical writer jobs pay per hour?
As of Jul 25, 2026, the average hourly pay for overnight 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 Overnight Biotech Technical Writer vs Biotech Scientific Writer?
| Aspect | Overnight Biotech Technical Writer | Biotech Scientific Writer |
|---|---|---|
| Credentials | Bachelor's degree in life sciences or related field; technical writing experience | Master's or PhD in life sciences; scientific research background |
| Work Environment | Fast-paced biotech companies, often overnight shifts for global teams | Research labs, academic institutions, or biotech firms, typically daytime hours |
| Employer & Industry Usage | Common in biotech firms requiring 24/7 documentation support | Used in research-focused roles, less common in overnight settings |
Overnight Biotech Technical Writers focus on creating clear documentation for biotech products during overnight shifts, often requiring quick turnaround and technical expertise. Biotech Scientific Writers generally work on research papers and scientific content during regular hours, with a stronger emphasis on research background. The roles overlap in industry but differ mainly in work hours and specific focus areas.
What cities are hiring for Overnight Biotech Technical Writer jobs? Cities with the most Overnight 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 Overnight Biotech Technical Writer jobs? States with the most job openings for Overnight Biotech Technical Writer jobs include:
Full-time
Posted 21 days ago
Job description
Job ID: 21-12907
Skills:
-Ability to write technical documents, and tenacious attention to detail and consistency, especially with respect to style, format, and layout for visual design simplicity is a must.
-Previous experience with documents in a regulatory environment is preferred and knowledge or experience in 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, Visio is required and knowledge of document management systems (e.g. Condor and Veeva), quality systems (Veeva) and document collaboration systems (e.g. SmartSheets) are beneficial.
-An aptitude for teamwork and the ability to collaborate effectively with leaders, engineers and subject matter experts is needed.
-Strong organizational and time-management skills; the ability to deliver under pressure; and the ability to work flexibly to support changing assignments and priorities in an independent and reliable manner.
-Exceptional written and oral communication skills.
-Proven ability to create strong working relationships with respect to cultural diversity and working styles.
-Demonstrated ability to organize and execute on a variety of assignments and action plans.
-Ability to translate complex concepts into written and visual documentation.
Education:
Minimum BA or BS (or equivalent) in English, biology, chemistry, pharmacy, or a related field, or previous experience working in the pharmaceutical field
Skills:
-Ability to write technical documents, and tenacious attention to detail and consistency, especially with respect to style, format, and layout for visual design simplicity is a must.
-Previous experience with documents in a regulatory environment is preferred and knowledge or experience in 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, Visio is required and knowledge of document management systems (e.g. Condor and Veeva), quality systems (Veeva) and document collaboration systems (e.g. SmartSheets) are beneficial.
-An aptitude for teamwork and the ability to collaborate effectively with leaders, engineers and subject matter experts is needed.
-Strong organizational and time-management skills; the ability to deliver under pressure; and the ability to work flexibly to support changing assignments and priorities in an independent and reliable manner.
-Exceptional written and oral communication skills.
-Proven ability to create strong working relationships with respect to cultural diversity and working styles.
-Demonstrated ability to organize and execute on a variety of assignments and action plans.
-Ability to translate complex concepts into written and visual documentation.
Education:
Minimum BA or BS (or equivalent) in English, biology, chemistry, pharmacy, or a related field, or previous experience working in the pharmaceutical field
About Intelliswift
Sourced by ZipRecruiter
Intelliswift is consumed with the love for the new. Once a leading staffing company, Intelliswift now possesses the expertise to build data-rich modern platforms, and to create sophisticated systems for data management and analytics for thinking and connected enterprises. We are a global leader in delivering Digital Product Engineering, Data Management & Analytics, Cloud, Digital Enterprise and MSP/VMS staffing solutions. Led by a team of highly passionate and techno-centric innovators, we consciously embed the spirit of loving and embracing everything new in what we do. We ardently believe that companies that Love the New are at an advantage of being ahead of the curve in this age of digital.
Industry
It services
Company size
1,001 - 5,000 Employees
Headquarters location
Newark, CA, US
Year founded
2001