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Contract Technical Writer Jobs in Kansas (NOW HIRING)

... Contract Research Organization services. It is one of the market leaders in certain testing and ... The BioPharma Technical Writer is responsible for developing, reviewing, and maintaining controlled ...

... Contract Research Organization services. It is one of the market leaders in certain testing and ... The BioPharma Technical Writer is responsible for developing, reviewing, and maintaining controlled ...

The Writer ensures information environment activities are doctrinally correct, comply with Rules ... Job Type: Part-Time On-Call, Exempt Contract Length: More than 1 year Core Government Services is ...

Collaborates with the Blue Orders writers to ensure multi domain operations and effects are ... Job Type: Part-Time On-Call, Exempt Contract Length: More than 1 year Core Government Services is ...

What We Look For In a Technical Writing Tutor * Advanced Subject Mastery: Deep knowledge of ... Varsity Tutors does not contract in: Alaska, California, Colorado, Delaware, Hawaii, Maine, New ...

What We Look For In a Technical Writing Tutor * Advanced Subject Mastery: Deep knowledge of ... Varsity Tutors does not contract in: Alaska, California, Colorado, Delaware, Hawaii, Maine, New ...

Strong technical writing, storyboarding, and database management skills. * Excellent communication ... Job Type: Part-Time On-Call, Exempt Contract Length: More than 1 year Core Government Services is ...

Technical Acumen * Enter individual contract review matters into legal department tracking system ... Prepare written consents and other corporate governance documentation as directed. Collaboration

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Contract Technical Writer information

See Kansas salary details

$88.7K

$98.1K

$105.7K

How much do contract technical writer jobs pay per year?

As of Aug 15, 2026, the average yearly pay for contract technical writer in Kansas is $98,103.00, according to ZipRecruiter salary data. Most workers in this role earn between $93,600.00 and $102,600.00 per year, depending on experience, location, and employer.

What are some common challenges faced by contract technical writers, and how can they be managed?

Contract technical writers often encounter challenges such as quickly adapting to new industries or technologies, working with limited project background, and managing communication with multiple stakeholders. To navigate these, it's important to ask targeted questions early, establish clear project expectations, and utilize available documentation and subject matter experts efficiently. Strong organizational skills and proactive communication are essential to delivering high-quality work within tight deadlines commonly found in contract roles.

What is a contract technical writer?

Contract technical writers are professionals hired on a temporary or project basis to create, edit, and manage technical documentation for organizations. They often work independently or through staffing agencies, producing materials such as user manuals, guides, software documentation, and standard operating procedures. Unlike full-time employees, contract technical writers typically work for a set period or until the completion of specific projects, offering flexibility for both the writer and the employer. Their expertise helps businesses clearly communicate complex information to users, clients, or internal teams.

What is the difference between Contract Technical Writer vs Technical Writer?

AspectContract Technical WriterTechnical Writer
CredentialsTypically requires a degree in English, Communications, or related field; certifications like STC are a plusSame as Contract Technical Writer, often with similar certifications
Work EnvironmentProject-based, often remote or on-site for specific clientsFull-time employment, may be remote or in-office
Employer & IndustryFreelance or consulting firms, tech companies, manufacturingCorporations, publishers, tech firms, government agencies
Search & Comparison IntentOften searched for project-based or freelance rolesTypically sought as full-time positions

The main difference between a Contract Technical Writer and a Technical Writer lies in employment type and work setup. Contract Technical Writers work on a project basis, often freelance or temporary, while Technical Writers are usually full-time employees. Both roles require similar skills, credentials, and industry experience, but their work arrangements differ significantly.

What are the key skills and qualifications needed to thrive as a contract technical writer, and why are they important?

To thrive as a Contract Technical Writer, you need strong writing, editing, and research skills, usually supported by a relevant degree or experience in technical communication. Familiarity with documentation tools like Microsoft Word, Adobe FrameMaker, MadCap Flare, and content management systems is typically required. Excellent attention to detail, time management, and the ability to communicate complex information clearly are vital soft skills for this role. These abilities ensure the creation of accurate, user-friendly documentation that meets project deadlines and client expectations.

What does a contract technical writer do?

Contract technical writers compose journal articles, instruction manuals, textbooks, and other documents with complex, technical information that needs to be explained in an easy-to-understand way. Unlike staff writers, contract technical writers are freelancers that work on a short- or long-term contract basis. In this role, you determine the scope of each writing project from your client, then collaborate with product designers and developers to understand what you are writing about. Once you gather the required information, you write and organize the document based on your target audience, adding photographs, drawings, charts, and diagrams as needed. Your documents are proofread and edited before they are published.

How much does a freelance technical writer make?

Freelance technical writers typically earn between $30 and $100 per hour, depending on experience, specialization, and project complexity. Many also charge per project or word, with rates varying based on industry and technical expertise. Experienced writers with specialized skills in tools like Markdown or DITA can command higher rates.

Are contract technical writers still in demand?

Contract technical writers are still in demand as companies seek skilled professionals to create clear documentation for products and services. Demand is driven by technology growth, regulatory requirements, and the need for updated user manuals, often requiring proficiency with tools like Markdown or XML. Opportunities are available across various industries, including software, manufacturing, and healthcare, with remote work options increasing flexibility for contract roles.

Is a contract technical writer a high paying job?

Contract technical writers can earn competitive pay, often based on their experience, technical skills, and the complexity of the documentation. Rates for contract work typically range from hourly to project-based fees and can be higher than salaried positions, especially for specialized industries or advanced tools like DITA or FrameMaker.

What are the most commonly searched types of Technical Writer jobs in Kansas?

The most popular types of Technical Writer jobs in Kansas are:

What are popular job titles related to Contract Technical Writer jobs in Kansas?

For Contract Technical Writer jobs in Kansas, the most frequently searched job titles are:

What cities in Kansas are hiring for Contract Technical Writer jobs?

Cities in Kansas with the most Contract Technical Writer job openings:

What are popular job titles related to Contract Technical Writer jobs in KS?

For Contract Technical Writer jobs in KS, the most frequently searched job titles are:

Infographic showing various Contract Technical Writer job openings in Kansas as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 7% Part Time, 5% Contract, and 1% Nights. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $98,103 per year, or $47.2 per hour.

Technical Writer

Eurofins

Lenexa, KS • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 21 days ago


Eurofins rating

7.4

Company rating: 7.4 out of 10

Based on 180 frontline employees who took The Breakroom Quiz

68th of 120 rated laboratories


Job description

Company Description
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description
The BioPharma Technical Writer is responsible for developing, reviewing, and maintaining controlled documentation that supports validation and laboratory operation activities. This role ensures that standard operating procedures (SOPs), forms, protocols, and other technical documents are accurate, clear, and compliant. The Technical Writer collaborates with cross-functional subject matter experts to manage documents, support quality initiatives, and promote consistency and continuous improvement.
Technical Writer Duties Include but are not Limited to the Following:
BioPharma Technical Writer I
  • Write and edit forms, protocols, reports, and procedures from existing templates under supervision.
  • Analyze documents to maintain continuity of style and content.
  • Perform updates and revisions to technical documents as instructed.
  • Work with Scientists, Regulatory Affairs, and Research and Development in a collaborative manner.
  • Other duties as assigned

BioPharma Technical Writer II
As above, plus:
  • Mentor/train new associates.
  • Write documents from templates with minimal assistance.
  • Create/modify document templates as needed.
  • Participate in additional training (specific technical/scientific writing, regulatory affairs, clinical trials, statistics specific scientific topics, etc.).
  • Participate in additional projects such as process improvement initiatives, presenting at a departmental meeting, etc.
  • Other duties as assigned

Qualifications
Basic Minimum Education Qualifications:
  • Bachelor's degree in medical laboratory sciences, biology, chemistry, or another relevant scientific discipline required.
  • Additional education, training, or professional experience in technical, scientific, medical, or regulatory writing is preferred.

Basic Minimum Work Requirements:
BioPharma Technical Writer I
  • Minimum of two (2) years of scientific or technical writing experience strongly preferred.
    • In lieu of technical writing experience, a minimum of four (4) years of experience in a regulated clinical laboratory environment or four (4) years of experience in regulatory affairs and/or quality assurance may be considered.
  • Knowledge of Good Documentation Practices (GDP) and regulated environments, including CLIA, CAP, and GLP preferred.
  • Experience authoring, revising, and maintaining controlled documents such as SOPs, test records, validation reports, validation protocols, and summary reports preferred.
  • Authorization to work in the United States indefinitely without restriction or sponsorship.

BioPharma Technical Writer II
  • Minimum of 6 years of experience in a dedicated Technical Writing role.
    • In lieu of specific technical writing experience, a minimum of 3 years working in a regulated clinical laboratory and 3 years of technical writing experience may be accepted.
  • Authorization to work in the United States indefinitely without restriction or sponsorship.

The Ideal Candidate Possesses the Following:
  • Demonstrated excellence in technical writing, grammar, editing, and document review.
  • Strong organizational skills, with the capacity to manage multiple priorities simultaneously while maintaining accuracy and consistently meeting client deadlines.
  • Strong attention to detail, critical thinking, and analytical skills, with a commitment to producing high-quality, error-free work.
  • Ability to collaborate effectively with cross-functional teams, including subject matter experts, laboratory operations, project management, quality personnel, and external clients, to develop, revise, and maintain compliant documentation.
  • Ability to work efficiently and independently with little or no supervision

Physical Requirements:
  • Physical dexterity sufficient to use hands, arms, and shoulders repetitively to operate a keyboard and other office equipment, use a telephone, access file cabinets and other items stored at various levels, including overhead
  • Ability to speak and hear well enough to communicate clearly and understandably with sufficient volume to ensure an accurate exchange of information in normal conversational distance, over the telephone, and in a group setting
  • Ability to continuously operate a personal computer for extended periods of time (4 or more hours)
  • Mental acuity sufficient to collect and interpret data, evaluate, reason, define problems, establish facts, draw valid conclusions, make valid judgments and decisions

The essential physical and mental requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Additional Information
Position is full-time working Monday - Friday, 8:00am - 5:00pm, additional hours as needed. Candidates currently living within a commutable distance of Lenexa, KS are encouraged to apply.
  • Excellent full-time benefits including comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays

Eurofins USA Clinical Trial Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

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About Eurofins

Sourced by ZipRecruiter

Industry

Scientific research and development services, biotechnology research and development and environmental consulting services

Company size

10,000+ Employees

Headquarters location

Leacock, PA, US