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Weekday Biotech Technical Writer Jobs (NOW HIRING)

CEDENT

Technical Writer

Springfield, NJ

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 ...

ASI Systems Engineering

GMP Technical Writer

Kenosha, WI · On-site

$60 - $75/hr

... biotech, or medical device manufacturing • Demonstrated experience authoring Deviation reports, CAPA records, and Change Control packages • Proficiency with electronic quality management systems ...

Intuitive

Technical Writer

Sunnyvale, CA

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 ...

Intuitive Surgical

Technical Writer

Sunnyvale, CA

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 ...

Intuitive

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 ...

Lancesoft

CMC Technical Writer

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 ...

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Weekday Biotech Technical Writer information

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$66

How much do weekday biotech technical writer jobs pay per hour?

As of Jun 22, 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 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 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 is the difference between Weekday Biotech Technical Writer vs Biotech Scientific Writer?

AspectWeekday Biotech Technical WriterBiotech Scientific Writer
Required CredentialsBachelor's in Life Sciences, Technical Writing experienceBachelor's or higher in Life Sciences, Scientific Writing experience
Work EnvironmentCorporate biotech settings, office-basedResearch labs, biotech companies, office-based
Employer & Industry UsageBiotech firms, pharmaceutical companiesResearch institutions, biotech firms
Common Search & ComparisonYesYes

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.

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.
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:
Weekday Biotech Technical Writer jobs near you
Infographic showing various Weekday Biotech Technical Writer job openings in the United States as of June 2026, with employment types broken down into 5% Locum Tenens, 47% Full Time, 32% Contract, and 16% Nights. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $81,001 per year, or $38.9 per hour.

Technical Writer

Stark Pharma Solutions Inc

Swiftwater, PA • On-site

Contractor

Posted 13 days ago

Job description

Hi,

My name is Karthik Mutyala, and I am a Recruitment Manager with Stark Pharma Solutions, specializing in opportunities across the Pharmaceutical, Biotechnology, Medical Device, and Life Sciences industries.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

You can also follow Stark Pharma Solutions on LinkedIn for the latest job updates:

https://www.linkedin.com/company/99455976/

Role: Technical Writer

Location: Swiftwater, PA

Duration: 6-Month Contract

Industry: 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 and quality-related content into user-friendly training materials and documentation. This role will work closely with cross-functional teams to create compliant documentation, training content, and process materials within a GMP-regulated environment.

The ideal candidate will have experience in technical writing, quality systems documentation, and digital system deployments within pharmaceutical, biotechnology, laboratory, or manufacturing environments.

Key Responsibilities

  • Develop, revise, and maintain technical documentation, training materials, and process-related content.
  • Convert technical and operational information into engaging training presentations, user guides, and instructional materials.
  • Review, edit, and update quality documents including:
  • Standard Operating Procedures (SOPs)
  • Work Instructions
  • Guidelines
  • Validation Master Plans
  • Quality System Documentation
  • Ensure all documentation complies with GMP, regulatory, and internal quality requirements.
  • Collaborate with Quality, IT, Laboratory, and Operations teams to gather information and create accurate documentation.
  • Support digital transformation initiatives by developing training materials for new system implementations.
  • Assist with document control activities and quality documentation updates.
  • Create visual content, process flows, diagrams, and presentations using PowerPoint and Visio.
  • Participate in training development and delivery activities as needed.

Required Qualifications

  • Bachelor's degree required; advanced degrees (Master's or PhD) are welcome.
  • Minimum 2+ years of experience in Technical Writing, Documentation Management, or a related role.
  • Experience working within GMP-regulated pharmaceutical, biotech, laboratory, or life sciences environments.

Hands-on experience with quality systems and applications such as:

  • Veeva
  • LIMS
  • LabWare (preferred)

Proficiency with:

  • Microsoft Word
  • Excel
  • PowerPoint
  • Visio
  • Outlook
  • Strong technical writing, editing, and document management skills.
  • Excellent verbal and written communication abilities.
  • Strong interpersonal skills with the ability to work effectively in cross-functional teams.