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 ...
Technical Writer / Manufacturing SOP Specialist (Biotech Drug Substance Operations)
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 ...
Technical Writer / Manufacturing SOP Specialist (Biotech Drug Substance Operations)
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 ...
Scientist-Technical Writer
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 ...
Scientist-Technical Writer
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 ...
Technical Writer
Cambridge, MA · On-site
... biotechnology or pharmaceutical industry Direct experience in GXP-compliant quality systems is ... Excellent communication skills including: technical writing, interpersonal and collaborative skills;
Technical Writer
Cambridge, MA · On-site
... biotechnology or pharmaceutical industry Direct experience in GXP-compliant quality systems is ... Excellent communication skills including: technical writing, interpersonal and collaborative skills;
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 ...
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 ...
Technical Writer
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 Writer
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 ...
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.
MSAT Process Technical Writer
Portsmouth, NH · On-site
Working experience of pharma/biotech (or equivalent) preferred. * Technical writing in the biotech industry preferred. * Project management skills a plus. * Strong MS Word experience preferred.
MSAT Process Technical Writer
Portsmouth, NH · On-site
Working experience of pharma/biotech (or equivalent) preferred. * Technical writing in the biotech industry preferred. * Project management skills a plus. * Strong MS Word experience 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.
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.
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.
Quick apply
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.
Technical Writer IV
South San Francisco, CA · On-site
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 IV
South San Francisco, CA · On-site
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 ...
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 ...
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 ...
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 ...
Weekday 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 weekday biotech technical writer jobs pay per hour?
As of Jun 1, 2026, the average hourly pay for weekday 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 are the key skills and qualifications needed to thrive as a Weekday Biotech Technical Writer, and why are they important?
To thrive as a Weekday Biotech Technical Writer, you need a solid background in biological sciences, strong writing skills, and familiarity with scientific documentation standards, usually supported by a relevant degree. Proficiency with document management systems, reference management tools, and regulatory submission platforms is commonly required. Attention to detail, excellent communication, and the ability to translate complex concepts into clear language are standout soft skills. These competencies ensure accurate, compliant, and accessible documentation critical for research, regulatory approval, and effective knowledge sharing in the biotech industry.
What are the primary challenges a Weekday Biotech Technical Writer faces when translating complex scientific information for diverse audiences?
A key challenge for Weekday Biotech Technical Writers is simplifying highly technical or scientific content while maintaining accuracy and compliance with regulatory standards. These writers often collaborate with scientists, engineers, and regulatory teams to ensure documentation is both understandable and comprehensive for different audiences, such as regulatory authorities or end-users. Balancing technical precision with readability, managing tight deadlines, and staying updated on evolving biotech terminology are common aspects of the role. Strong communication skills and adaptability are essential to bridge gaps between subject matter experts and non-technical stakeholders.
What does a Weekday Biotech Technical Writer do?
A Weekday Biotech Technical Writer is responsible for creating, editing, and maintaining technical documents related to biotechnology, such as protocols, standard operating procedures, research summaries, and regulatory submissions. They collaborate with scientists, engineers, and regulatory specialists to ensure accuracy and clarity in all written materials. Typically, this role is performed during standard business days (Monday through Friday), supporting the communication needs of biotech companies or research organizations.
What is the difference between Weekday Biotech Technical Writer vs Biotech Scientific Writer?
| Aspect | Weekday Biotech Technical Writer | Biotech Scientific Writer |
|---|---|---|
| Required Credentials | Bachelor's in Life Sciences, Technical Writing experience | Bachelor's or higher in Life Sciences, Scientific Writing experience |
| Work Environment | Corporate biotech settings, office-based | Research labs, biotech companies, office-based |
| Employer & Industry Usage | Biotech firms, pharmaceutical companies | Research institutions, biotech firms |
| Common Search & Comparison | Yes | Yes |
The Weekday Biotech Technical Writer primarily focuses on creating clear, concise technical documentation for biotech products and processes within corporate settings. In contrast, the Biotech Scientific Writer often emphasizes scientific research papers, publications, and detailed scientific content. Both roles require similar educational backgrounds and industry experience, but their main outputs and work environments differ slightly, with technical writers more involved in documentation for product development and scientific writers more engaged in research dissemination.
More about Weekday Biotech Technical Writer jobs
What cities are hiring for Weekday Biotech Technical Writer jobs? Cities with the most Weekday 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 Weekday Biotech Technical Writer jobs? States with the most job openings for Weekday Biotech Technical Writer jobs include:
What job categories do people searching Weekday Biotech Technical Writer jobs look for? The top searched job categories for Weekday Biotech Technical Writer jobs are:
Job description
Company Description
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Job Description
Looking for someone to provide technical writing support to a process development technical team - drafting documents, editing, working with scientists to enter figures etc. Prior experience in biotechnology area/ cell therapy area preferred good oral and written communication skills.
Qualifications
Bachelor's degree (Science or writing area )
Additional Information
Feel free to forward my email to your friends/colleagues who might be available. We do offer a referral bonus!!
Thank you for your time and for consideration. I look forward to hearing from you
Thanks!!
With Regards,
Shiva Kapoor
Technical Recruiter
Direct: 732-429-1929
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About Integrated Resources
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996