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Biotech Technical Writer Jobs in Chicago, IL (NOW HIRING)

Frontage Laboratories

Report Writer

Chicago, IL · On-site

$21.63 - $25.97/hr

Technical Report Supervisor Full-time Frontage Laboratories Inc. is an award winning, full-service ... biotechnology products. Position/Job Summary: This position supports toxicologists in their ...

New

Capstone Search Partners

Patent Agent

Des Plaines, IL

$110K - $210K/yr

S. and international patent applications in the life sciences sector, including biotechnology ... Excellent technical writing and analytical skills with a keen attention to detail. * Ability to ...

Pioneer GMP Consulting

CQV Engineer (Chicago)

Chicago, IL · On-site

$110 - $150/hr

... biotech manufacturing environments in the Chicago area. As part of our consulting team, you'll ... Strong technical writing skills , including protocol execution, report generation, deviations, and ...

New

IMA Automation USA Inc

Service Controls Engineer

Elgin, IL · On-site

$83K - $107K/yr

Technical understanding of pharmaceutical / biotechnology unit operations a plus. * Fundamental ... Strong technical writing, communication and interpersonal skills required. * Ability to travel 75 ...

IMA Automation USA Inc

Service Controls Engineer

Elgin, IL · On-site

$83K - $107K/yr

Technical understanding of pharmaceutical / biotechnology unit operations a plus. * Fundamental ... Strong technical writing, communication and interpersonal skills required. * Ability to travel 75 ...

IMA Automation USA Inc

Service Controls Engineer

Elgin, IL · On-site

$35 - $40/hr

Technical understanding of pharmaceutical / biotechnology unit operations a plus. * Fundamental ... Strong technical writing, communication and interpersonal skills required. * Ability to travel 25 ...

Clayco (LJC)

Project Architect - Life Sciences

Chicago, IL · On-site

$85K - $114K/yr

This role is responsible for the technical leadership, coordination, and execution of architectural ... Strong written and verbal communication skills, including participation in client-facing ...

Clayco

Project Architect - Life Sciences

Chicago, IL · On-site

$85K - $114K/yr

This role is responsible for the technical leadership, coordination, and execution of architectural ... Strong written and verbal communication skills, including participation in client-facing ...

Clayco (LJC)

Project Architect - Life Sciences

Chicago, IL · On-site

$85K - $114K/yr

This role is responsible for the technical leadership, coordination, and execution of architectural ... Strong written and verbal communication skills, including participation in client-facing ...

Clayco (LJC)

Project Architect - Life Sciences

Chicago, IL · On-site

$85K - $114K/yr

This role is responsible for the technical leadership, coordination, and execution of architectural ... Strong written and verbal communication skills, including participation in client-facing ...

Clayco (LJC)

Project Architect - Life Sciences

Chicago, IL

$85K - $114K/yr

This role is responsible for the technical leadership, coordination, and execution of architectural ... Strong written and verbal communication skills, including participation in client-facing ...

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Biotech Technical Writer information

See Chicago, IL salary details

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How much do biotech technical writer jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for biotech technical writer in Chicago, IL is $40.12, according to ZipRecruiter salary data. Most workers in this role earn between $29.71 and $48.56 per hour, depending on experience, location, and employer.

What is a biotech technical writer?

A Biotech Technical Writer creates clear, accurate, and concise documentation related to biotechnology, such as research reports, regulatory submissions, standard operating procedures (SOPs), and product manuals. They translate complex scientific concepts into understandable content for various audiences, including researchers, regulators, and the general public. This role requires strong writing skills, attention to detail, and knowledge of biotech terminology and industry regulations. Biotech Technical Writers often collaborate with scientists, engineers, and regulatory professionals to ensure documentation meets industry standards.

What are the key skills and qualifications needed to thrive as a biotech technical writer?

To thrive as a Biotech Technical Writer, you need a solid understanding of scientific concepts, excellent written communication skills, and often a degree in life sciences, biotechnology, or a related field. Familiarity with document management systems, scientific publishing software, and regulatory compliance guidelines such as Good Laboratory Practices (GLP) or FDA requirements is typically required. Strong attention to detail, adaptability, and the ability to collaborate with cross-functional teams are essential soft skills in this position. These competencies are crucial for effectively translating complex scientific content into clear, accurate documentation that supports research, product development, and regulatory submissions.

What are the common challenges faced by biotech technical writers in their daily work?

Biotech Technical Writers often encounter the challenge of translating highly technical and complex scientific data into clear, concise documents for diverse audiences, including regulatory agencies and non-specialist stakeholders. They must stay up-to-date with evolving regulations and industry best practices, which can be demanding in a rapidly changing biotech landscape. Additionally, working closely with subject matter experts from research, development, and regulatory teams requires strong collaboration and communication skills to ensure accuracy and consistency. Overcoming these challenges not only sharpens your abilities but also makes you an invaluable asset within interdisciplinary biotech environments.

What are the most commonly searched types of Biotech Technical Writer jobs in Chicago, IL?

The most popular types of Biotech Technical Writer jobs in Chicago, IL are:

What are popular job titles related to Biotech Technical Writer jobs in Chicago, IL?

For Biotech Technical Writer jobs in Chicago, IL, the most frequently searched job titles are:

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Biotech Technical Writer jobs near you
Infographic showing various Biotech Technical Writer job openings in Chicago, IL as of August 2026, with employment types broken down into 72% Full Time, and 28% Contract. Highlights an 65% In-person, 12% Hybrid, and 23% Remote job distribution, with an average salary of $83,443 per year, or $40.1 per hour.

Report Writer

Frontage Laboratories

Chicago, IL • On-site

$21.63 - $25.97/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 2 days ago

New

Job description

Report Writer

 

Title: Report Writer

Location: Chicago, IL, onsite

Reports to: Technical Report Supervisor

 

Full-time

 

Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.


Our Chicago, IL site provides toxicology testing and research laboratory services and specialized pre-clinical studies in support of pharmaceutical and biotechnology products.


Position/Job Summary: 

This position supports toxicologists in their preparation and presentation of reports, protocols or other documents associated with the evaluation of the safety and/or toxicity of various materials (e.g., pharmaceuticals, chemicals, etc.). The Report Writer prepares documents from information provided by personnel and/or subcontractors to be submitted to Study Sponsors. In addition to preparation of text, this position requires tabulation and summarization of data as well as some interpretation of results. Writers receive assignments from Study Directors and Management and are supervised by the Technical Writing Supervisor.


Roles & Responsibilities:


  • Generating, formatting, and, reviewing pre-clinical main study reports and sub-reports.
  • Coordinating and facilitating the compilation of report information from the Frontage study team (e.g., Study Directors, Study Supervisors, Management, and Quality Assurance personnel), Principal Investigators, and Contributing Scientists. 
  • Maintain consistent formatting across all Sponsor-facing documents by adhering to current style guidelines. 
  • Set up and troubleshoot table template generation for data outputs as well as quality check outputs for formatting/data errors.
  • Compile, organize, and present collected study data in a logical manner within summary and appendix sections of reports/sub-reports, as well as appropriately creating/linking in-text references to appended data.
  • Maintaining technical information in both electronic and paper formats. 
  • Generating new documents from pre-established template files following pre-established guidelines in their implementation and maintenance, or creating/maintaining new templates as needed. 
  • Tracking the preparation of report or other documents (e.g., protocols, study specific procedures) as well as the progress of study data as it is prepared for reports.
  • Maintaining open lines of communication within the reporting writing team, Study Directors, Quality Assurance, and Management regarding the status of reports/documents and data processing. 
  • Identifying and resolving problems related to the production of reports and other documents. 
  • Maintaining an understanding of pertinent governmental regulations (e.g., FDA, EPA, OECD, ICH, etc.), data handling best practices, and Sponsor guidelines.
  • Delivering assignments on time and adjusting regular business hours to accommodate deadlines. 


Education, Experience & Skills Required:

 

  • Must have a minimum of a BS/BA degree in a science/related discipline or prior experience that contributes directly and significantly to the individual’s technical writing competence. 
  • Experience with electronic document management; proficiency in Microsoft Word (general operation/document formatting) and Excel required.
  • Familiarity with Adobe Acrobat and Photoshop, or equivalent, for report compilation and finalization processes preferred.
  • Must possess strong organizational, grammatical, editorial/proofreading, reading comprehension, and critical thinking skills.
  • Must be able self-start independent work, cooperatively interact with study team members toward common goals, and to work on multiple projects concurrently. 
  • Must possess excellent communication skills to effectively interact with other personnel.
  • Familiarity with adherence to protocol/SOP-specified parameters preferred.


Salary: $21.63-$25.97/hour


Benefits:

  • 401k Employer Match with immediate vesting
  • Vision Insurance 
  • Medical and Dental Insurance with multiple coverage options
  • FSA (Medical, Dependent Care, and Commuter)
  • Short Term Disability
  • Long Term Disability 
  • Life Insurance
  • Generous Paid Holidays and PTO 

 

Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.