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Weekday Biotech Technical Writer Jobs (NOW HIRING)

Perrigo

Technical Writer-LMS Administrator

Bronx, NY

$75K - $80K/yr

The Technical Writer will partner with Quality department, other cross functional managers ... Possesses basic technical knowledge and background in the pharmaceutical and biotechnology industry

ESI Total Fuel Management

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Instructional Designer / Technical Writer

Reston, VA · On-site

$90K - $110K/yr

Strong written and verbal communication skills * Experience creating technical and instructional ... Birthday off when it falls on a weekday * Paid volunteer service time * Company donation matching ...

ESI Total Fuel Management

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Instructional Designer / Technical Writer

Ashburn, VA · On-site

$90K - $110K/yr

Strong written and verbal communication skills * Experience creating technical and instructional ... Birthday off when it falls on a weekday * Paid volunteer service time * Company donation matching ...

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Weekday Biotech Technical Writer information

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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?

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.

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 May 2026, with employment types broken down into 99% Full Time, and 1% Part Time. Highlights an 10% Physical, and 90% Remote job distribution, with an average salary of $81,001 per year, or $38.9 per hour.

Technical Writer-LMS Administrator

Perrigo Company plc

Bronx, NY • On-site

$75K - $80K/yr

Full-time

Posted 25 days ago

Perrigo rating

8.4

Company rating: 8.4 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

20th of 71 rated pharmaceutical

Job description

Description Overview
The Technical Writer is responsible for the development, creation, and revision of controlled documentation using the OpenText System in accordance with Perrigo policies and procedures and current GMP practices. The Technical Writer will partner with Quality department, other cross functional managers/supervisors, and engineers to ensure that controlled documents being revised contain the correct information. Additionally, the role will provide support for maintaining the Learning Management System (LMS).
The salary range for this role is between $75,000 to $80,000
Scope of the Role
  • Support/Train functional departments and subject matter experts in the creation and revision of the following cGMP documentation to optimize processing and ensure alignment with current practices utilizing the OpenText system:
    • Standard Operating Procedures
    • Standard Work Instructions
    • Training Completion Statements,
    • Job Aids
    • Controlled Forms
  • Execute tasks associated with LMS administration, including but not limited to the creation and maintenance of:
    • Creates and maintains GMP curricula, courses, and items.
    • Enter training records in the LMS system or using the ATA system
    • Generate and track the audit of each curriculum working with department heads or curriculum owner
    • Provides training reports , training material and metrics as requested for compliance to support FDA audit, internal/external audit and miscellaneous requests.
    • Recognizes and resolves training discrepancies, reaches out to Global training and communicates corrective action to affected personnel.
  • Review cGMP documentation for standardized formatting, technical accuracy, clarity, grammar, and spelling.
  • Select and edit images/videos (photographs, diagrams, technical drawings) to enhance training materials.
  • Files all training documentation (hard copy) and provides general administrative support for the department as required.
  • Excellent understanding and working knowledge of PC and Microsoft applications (Microsoft Office) and presentation tools (PowerPoint).
  • Details oriented with the ability to multi-task and meet deadlines as well as strong interpersonal and team building skills.
  • Strong organizational skills, flexibility, and ability to work independently.
  • Administration duties:
    • Member of the site committees
    • Ordering supplies/decorations, lunches, catering
    • Utilizing the RedZone system to post communication, recognition and site event
    • Oversee the Company store, working with Operations, Manufacturing and Warehouse with scheduling of employees

Experience Required
  • Bachelor's degree.
  • 2 or more years of relevant systems experience required in a regulated industry, preferably in Life Sciences.
  • Learning Management System (LMS).
  • Understands the application of GMP concepts and understands 'why' behind the regulations.
  • Possesses basic technical knowledge and background in the pharmaceutical and biotechnology industry
  • Comprehensive working knowledge of OpenText, Microsoft suite, including Outlook, Teams, Word, Excel, PowerPoint, SharePoint

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