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
Aberdeen Proving Ground, MD · On-site
$51K - $82K/yr
Perform high quality technical writing, editing, and formatting of deliverables/documents, to ... Occasional overnight travel #PLABS26 Qualifications * Active Secret clearance and ability to obtain ...
Technical Writer
Aberdeen Proving Ground, MD · On-site
$51K - $82K/yr
Perform high quality technical writing, editing, and formatting of deliverables/documents, to ... Occasional overnight travel #PLABS26 Qualifications * Active Secret clearance and ability to obtain ...
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 ...
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 ...
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 ...
New
Technical Writer
Fenton, MI · On-site
Ability to read technical journals, abstracts, manuals and specifications in a timely manner with ... Training may involve daily travel to the customer facility or depending on location, overnight stay ...
Technical Writer
Fenton, MI · On-site
Ability to read technical journals, abstracts, manuals and specifications in a timely manner with ... Training may involve daily travel to the customer facility or depending on location, overnight stay ...
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
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 ...
Significant working experience (>6 years) in pharmaceutical/biotech CMC and analytical development ... Strong organization and technical writing skills * High attention to detail and scientific rigor
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Significant working experience (>6 years) in pharmaceutical/biotech CMC and analytical development ... Strong organization and technical writing skills * High attention to detail and scientific rigor
... 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 ...
Technical Writer - Freelance
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
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Technical Writer - Freelance
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
... 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 ...
Minimum of two (2) years of experience in Pharmaceutical, Medical Device or Biotech environment ... Independently write complex technical reports, describing investigation results and complete ...
Minimum of two (2) years of experience in Pharmaceutical, Medical Device or Biotech environment ... Independently write complex technical reports, describing investigation results and complete ...
... 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 ...
Minimum of two (2) years of experience in Pharmaceutical, Medical Device or Biotech environment ... Independently write complex technical reports, describing investigation results and complete ...
Minimum of two (2) years of experience in Pharmaceutical, Medical Device or Biotech environment ... Independently write complex technical reports, describing investigation results and complete ...
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 Jun 10, 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:
Job description
Summary: Reporting to the appropriate department based on area of expertise (Quality Assurance, Quality Control, or Manufacturing). We are seeking a detail-oriented and highly skilled GMP Pharmaceutical Technical Writer to join our team. The ideal candidate will be responsible for creating, revising, and maintaining various controlled documentation that complies with Good Manufacturing Practices (GMP) regulations and industry standards.
This role will work closely with internal and client cross-functional teams, including quality assurance, regulatory, production, and project management, to ensure timely delivery, accuracy, and clarity of all technical documents essential for the manufacturing and regulatory processes in a pharmaceutical industry. Responsibilities: Technical Documentation: Author, edit, and maintain a wide range of documents, including Standard Operating Procedures (SOPs), batch records, validation protocols, technical reports, change control documents, and regulatory submissions in accordance with GMP guidelines. Compliance: Ensure all written materials meet regulatory and GMP requirements, and align with the company's quality standards, procedures, and policies.
Collaboration: Work closely with both Client stakeholders and client stakeholders to establish alignment on deliverables and ensure project timelines are maintained. Document Management: Assist in the management of controlled documents in document control systems (e.g., electronic document management systems), ensuring traceability, version control, and appropriate distribution of approved documents. Process Improvement: Participate in process improvement initiatives related to document control, writing standards, and compliance, ensuring continuous enhancement of documentation practices
Audits & Inspections: Support internal and external audits by preparing relevant documentation and ensuring that all technical writing adheres to current regulatory standards. Change Control: Document and track changes in manufacturing processes, equipment, and methodologies, ensuring updates to procedures and records are properly reflected. Essential Education and Qualifications: Education: Bachelor's degree in Life Sciences, Chemistry, Pharmaceutical Sciences, Engineering, or a related field.
Advanced degree or certification in technical writing is a plus. 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 documentation, including SOPs, validation protocols, and reports.
Knowledge: Solid understanding of GMP regulations (FDA, EMA, ISO, ICH, etc.) and regulatory requirements for pharmaceutical manufacturing. Proficiency with document management systems and Microsoft Office Suite (Word, Excel, PowerPoint). Skills: Exceptional written and verbal communication skills, with a strong ability to translate complex technical concepts into clear, concise documentation
Detail-oriented with strong organizational and project management skills. Ability to work independently, manage multiple projects simultaneously, and meet deadlines in a fast-paced environment. Strong analytical and problem-solving skills, with the ability to work cross-functionally across departments.
About Cedent
Sourced by ZipRecruiter
CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.
Industry
It services
Company size
11 - 50 Employees
Headquarters location
Plano, TX, US
Year founded
2008