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Manufacturing Technical Writer Jobs in Kansas (NOW HIRING)

Eurofins

Technical Writer

Lenexa, KS · On-site

... Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and ... The BioPharma Technical Writer is responsible for developing, reviewing, and maintaining controlled ...

Eurofins Scientific

Technical Writer

Lenexa, KS

... Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and ... The BioPharma Technical Writer is responsible for developing, reviewing, and maintaining controlled ...

Sunbelt Solomon

Lead

Solomon, KS · On-site

$25 - $26/hr

Previous experience working in a manufacturing/technical environment. * Ability to obtain a hoist and Forklift license. * Ability to write simple correspondence. * Ability to effectively present ...

Sunbelt Solomon

Lead

Solomon, KS · On-site

Previous experience working in a manufacturing/technical environment. * Ability to obtain a hoist and Forklift license. * Ability to write simple correspondence. * Ability to effectively present ...

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Manufacturing Technical Writer information

What are the key skills and qualifications needed to thrive in the manufacturing technical writer position, and why are they important?

A Manufacturing Technical Writer should possess strong writing, editing, and document management skills, often supported by a degree in technical communication, engineering, or a related field. Familiarity with authoring tools such as Adobe FrameMaker, MadCap Flare, and knowledge of Document Control Systems (DCS) or Product Lifecycle Management (PLM) are commonly required, along with certifications like CPTC. Excellent communication, attention to detail, and the ability to quickly grasp complex manufacturing processes make candidates stand out. These competencies ensure technical documentation is accurate, clear, and effectively supports safe and efficient manufacturing operations.

What are the typical daily responsibilities of a manufacturing technical writer?

As a Manufacturing Technical Writer, your daily responsibilities typically include researching complex machinery or production processes, creating and updating instruction manuals, standard operating procedures, and safety documentation. You will frequently collaborate with engineers, production managers, and quality assurance teams to gather accurate information and ensure documentation reflects current practices. Reviewing and testing documents for clarity and usability, maintaining version control, and complying with industry or regulatory standards are also central to the role. This position requires a proactive approach to communication and a commitment to continuous improvement in documentation practices.

What is a manufacturing technical writer?

A Manufacturing Technical Writer creates clear and concise documentation for manufacturing processes, equipment, and standards. They develop user manuals, work instructions, and technical guides to ensure accurate production and compliance. Their role involves collaborating with engineers, operators, and quality teams to translate complex technical details into understandable content. Strong writing, technical expertise, and attention to detail are essential for success in this role.

Are manufacturing technical writers still in demand?

Manufacturing technical writers are still in demand as companies require clear documentation for complex machinery, processes, and safety procedures. They often work closely with engineers and use tools like Adobe FrameMaker or MadCap Flare, with demand driven by manufacturing industry growth and technological advancements.

What is technical writing in manufacturing?

Technical writing in manufacturing involves creating clear, detailed documentation such as user manuals, standard operating procedures, and technical reports to communicate complex processes and equipment instructions. It requires strong writing skills, understanding of manufacturing processes, and often the use of tools like CAD or documentation software. This role helps ensure safety, compliance, and efficient operation within manufacturing environments.

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

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

What job categories do people searching Manufacturing Technical Writer jobs in Kansas look for?

The top searched job categories for Manufacturing Technical Writer jobs in Kansas are:

Manufacturing Technical Writer jobs near you
Infographic showing various Manufacturing 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.

Technical Writer

Eurofins

Lenexa, KS • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 23 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.

What Eurofins employees say

Pay

Benefits

Hours and flexibility

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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

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