ZipRecruiter

Log In

1

Technical Contract Manager Jobs in Kansas (NOW HIRING)

Eurofins

Technical Writer

Lenexa, KS · On-site

... Contract Research Organization services. It is one of the market leaders in certain testing and ... The Technical Writer collaborates with cross-functional subject matter experts to manage documents ...

Eurofins Scientific

Technical Writer

Lenexa, KS

... Contract Research Organization services. It is one of the market leaders in certain testing and ... The Technical Writer collaborates with cross-functional subject matter experts to manage documents ...

previous pagenext page

Showing results 21-40

All JobsTechnical Contract JobsTechnical Contract Manager JobsTechnical Contract Manager Jobs in Kansas

Technical Contract Manager information

Are technical contract managers in demand?

Technical contract managers are in demand due to the need for specialized skills in managing complex technology contracts, ensuring compliance, and coordinating between technical teams and clients. The role is often found in industries such as IT, engineering, and construction, with demand driven by ongoing project growth and regulatory requirements.

Is a technical contract manager a stressful job?

A technical contract manager often faces stress due to managing complex contracts, deadlines, and stakeholder expectations. The role requires strong organizational skills, attention to detail, and the ability to handle multiple priorities, which can contribute to a high-pressure environment.

What are the key skills and qualifications needed to thrive as a technical contract manager?

To thrive as a Technical Contract Manager, you need a solid background in contract law, negotiation, and project management, often supported by a degree in business, law, or engineering. Familiarity with contract management software, ERP systems, and relevant industry certifications such as CIPS or IACCM is typically required. Exceptional attention to detail, strong communication, and problem-solving skills set top performers apart in this role. These abilities are crucial for minimizing risk, ensuring compliance, and facilitating successful project outcomes in complex technical environments.

What are some common challenges technical contract managers face when coordinating between technical teams and legal departments?

Technical Contract Managers often encounter challenges in bridging the gap between technical teams and legal departments, as each group has its own language and priorities. Translating technical requirements into contract terms that are both legally sound and technically feasible can be complex. Successful managers develop strong communication skills and a keen attention to detail to ensure all stakeholders are aligned, minimizing misunderstandings and project delays. Building relationships across departments and staying updated on both technical trends and contract law are key to overcoming these challenges.

What is a technical contract manager?

A Technical Contract Manager is responsible for overseeing and managing contracts that involve technical products, services, or projects. They ensure that all contractual obligations are met, coordinate between technical teams and clients, and handle contract negotiations, renewals, and compliance issues. This role requires strong technical knowledge, attention to detail, and excellent communication skills to bridge the gap between legal, procurement, and engineering departments.

Is a technical contract manager a good career?

A technical contract manager is a valuable role that involves overseeing contractual agreements in technical industries, requiring skills in negotiation, legal understanding, and project management. It offers opportunities for career growth, especially in engineering, IT, and construction sectors, often with competitive salaries and certifications like CPCM or CFCM. Success in this career depends on experience, industry demand, and the ability to manage complex projects effectively.

What is the difference between Technical Contract Manager vs Contract Specialist?

AspectTechnical Contract ManagerContract Specialist
CredentialsTypically requires a bachelor's degree in engineering, business, or related field; certifications like CPCM or NCMA are commonUsually holds a bachelor's degree in business, law, or related field; certifications like CPCM or NCMA are also common
Work EnvironmentWorks closely with technical teams, legal, and procurement in industries like engineering, construction, or ITFocuses on contract administration, review, and compliance within various industries, often in government or corporate settings
Employer & Industry UsageUsed by engineering firms, government agencies, and large corporations managing technical projectsCommon in government contracting, corporate procurement, and legal departments

The Technical Contract Manager and Contract Specialist roles share similar credentials and often work within the same industries. However, the Technical Contract Manager typically handles more complex technical negotiations and project oversight, while the Contract Specialist focuses on contract administration and compliance. Both roles are essential in managing contractual relationships in technical and procurement environments.

What job categories do people searching Technical Contract Manager jobs in Kansas look for? The top searched job categories for Technical Contract Manager jobs in Kansas are:
What cities in Kansas are hiring for Technical Contract Manager jobs? Cities in Kansas with the most Technical Contract Manager job openings:
Technical Contract Manager jobs near you

Technical Writer

Eurofins

Lenexa, KS • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 15 days ago

Eurofins rating

7.4

Company rating: 7.4 out of 10

Based on 180 frontline employees who took The Breakroom Quiz

69th 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

Workplace

Get the full story on Breakroom

Eurofins logo

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

View All Eurofins Jobs

Apply