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Senior Validation Engineer Jobs in Kansas (NOW HIRING)

SUMMARY The Senior Technical Recruiter at Axius Group is a senior level individual contributor ... Evaluates and validates engineering and information technology technical capability at an advanced ...

Valid driver's license and favorable driving record required * PTOE certification preferred Senior Traffic Engineer Salary Range: $97,594 to $138,219 * Bachelor's degree in civil engineering or a ...

Sr. Electrical Engineer

Kansas City, KS · On-site

$101K - $132K/yr

Position Summary The Senior Electrical Engineer will work within the engineering team to design, analyze, and validate electrical systems and components for OrangeEV's product lines. This role ...

Sr. Electrical Engineer

Kansas City, KS · On-site

$101K - $132K/yr

Position Summary The Senior Electrical Engineer will work within the engineering team to design, analyze, and validate electrical systems and components for OrangeEV's product lines. This role ...

Senior Plant Engineer

Shawnee, KS · On-site

$86K - $117K/yr

Argenta is currently looking to fill the role of Senior Plant Engineer at our Shawnee, KS location ... Reviews and approves standard operating procedures describing validation principles and activities.

Senior Plant Engineer

Shawnee, KS · On-site

$86K - $117K/yr

Argenta is currently looking to fill the role of Senior Plant Engineer at our Shawnee, KS location ... Reviews and approves standard operating procedures describing validation principles and activities.

Senior Software Engineer

Overland Park, KS · On-site

$121K - $159K/yr

As an Senior Software Engineer, Technical Lead, on the New Annuity Products teamyou are the ... to validate integration points. * Tech Debt Strategy. Identify, prioritize, and drive down ...

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Showing results 21-40

Senior Validation Engineer information

See Kansas salary details

$31

$57

$88

How much do senior validation engineer jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for senior validation engineer in Kansas is $57.77, according to ZipRecruiter salary data. Most workers in this role earn between $46.11 and $65.62 per hour, depending on experience, location, and employer.

What does a senior validation engineer do?

A Senior Validation Engineer is responsible for ensuring that products, systems, or processes meet regulatory standards and function as intended. They develop and execute validation protocols, analyze test data, and document results to confirm compliance with industry and company standards. Senior Validation Engineers often lead validation projects, collaborate with cross-functional teams, and mentor junior staff. Their work is critical in industries like pharmaceuticals, biotechnology, and manufacturing, where product safety and efficacy are essential.

What are the key skills and qualifications needed to thrive as a senior validation engineer, and why are they important?

To thrive as a Senior Validation Engineer, you need a solid background in engineering, quality assurance, and regulatory compliance, typically supported by a relevant degree and experience in validation within regulated industries. Familiarity with validation protocols (IQ, OQ, PQ), statistical analysis tools, and systems like FDA 21 CFR Part 11 is crucial. Strong problem-solving, attention to detail, and effective communication skills help ensure successful project outcomes and cross-functional collaboration. These skills and qualifications are essential to maintain product quality, meet regulatory standards, and drive continuous improvement.

What are some typical challenges faced by senior validation engineers when leading validation projects?

Senior Validation Engineers often encounter challenges such as managing tight project timelines, ensuring compliance with evolving regulatory standards, and coordinating cross-functional teams. Balancing the needs of production, quality assurance, and regulatory affairs requires strong communication and project management skills. Additionally, troubleshooting unexpected validation failures and documenting results thoroughly are key aspects that demand both technical expertise and attention to detail.

What is the difference between Senior Validation Engineer vs Validation Specialist?

AspectSenior Validation EngineerValidation Specialist
CredentialsBachelor's or Master's in Engineering, Life Sciences, or related fields; often with certifications like GxP or CSVSimilar educational background; certifications like GxP or CSV are common
Work EnvironmentDesigns and oversees validation protocols in manufacturing, biotech, or pharmaceutical settingsExecutes validation tasks, tests, and documentation in similar environments
Employer & IndustryPharmaceutical, biotech, medical device companiesSame industries, often working under validation teams
Search & ComparisonOften compared for experience level and responsibilitiesCommonly searched together for validation roles

The main difference is that a Senior Validation Engineer typically leads validation projects, designs protocols, and oversees validation activities, while a Validation Specialist focuses on executing validation tests and documentation. Both roles require similar credentials and work in comparable environments, but the Senior Validation Engineer has more responsibility for planning and oversight.

What are the most commonly searched types of Validation Engineer jobs in Kansas?

The most popular types of Validation Engineer jobs in Kansas are:

What are popular job titles related to Senior Validation Engineer jobs in Kansas?

For Senior Validation Engineer jobs in Kansas, the most frequently searched job titles are:

What job categories do people searching Senior Validation Engineer jobs in Kansas look for?

The top searched job categories for Senior Validation Engineer jobs in Kansas are:

What cities in Kansas are hiring for Senior Validation Engineer jobs?

Cities in Kansas with the most Senior Validation Engineer job openings:

Infographic showing various Senior Validation Engineer job openings in Kansas as of August 2026, with employment types broken down into 85% Full Time, and 15% Contract. Highlights an 95% In-person, and 5% Remote job distribution, with an average salary of $120,156 per year, or $57.8 per hour.

Sr. Associate, Quality Assurance Validation

Elanco Animal Health Incorporated

Elwood, KS • On-site

Full-time

Retirement

Re-posted 24 days ago


Elanco rating

7.8

Company rating: 7.8 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

50th of 86 rated pharmaceutical


Job description

At Elanco (NYSE: ELAN) - it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose - all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals' lives better makes life better - join our team today!
Your Role: Sr. Associate, Quality Assurance Validation
The Sr. Associate, Quality Assurance Validation serves as a key Quality representative supporting capital projects, commissioning, qualification, and computer system validation (CSV) activities at the Elwood, Kansas monoclonal antibody (mAb) manufacturing facility. This role partners closely with engineering, validation, and cross-functional teams to ensure facilities, utilities, equipment, and systems are designed, qualified, and maintained in compliance with regulatory requirements. The position plays a critical role in ensuring data integrity, regulatory readiness, and adherence to cGMP standards while supporting the full lifecycle of capital and validation projects.
Your Responsibilities:
  • Provide Quality oversight for capital projects by actively participating as the QA representative throughout the project lifecycle, from design through qualification and validation. Support the design, engineering, commissioning, and qualification of facilities, utilities, equipment, and computerized systems used in mAb manufacturing.
  • Review and approve validation lifecycle documentation, including User Requirements, Design Qualifications, FAT/SAT, IQ/OQ/PQ protocols, reports, procedures, and periodic reviews. Provide guidance on qualification and validation strategies to engineering and quality teams to ensure compliance and consistency.
  • Support and oversee computer system validation (CSV) activities and contribute to maintaining and improving data integrity processes across the site. Drive continuous improvement and standardization of equipment and system lifecycle documentation aligned with Elanco operational standards.
  • Ensure compliance with cGMP and regulatory requirements by performing Quality review and oversight of site documentation. Support internal audits and regulatory inspections as needed, and promote a "Safety First and Quality Always" culture across all activities.

What You Need to Succeed (minimum qualifications):
  • Education: Bachelor's degree in a science or engineering discipline.
  • Experience: 5+ years of experience in quality, engineering, or validation roles within the biologics or pharmaceutical industry. Experience in equipment lifecycle management and computer system validation (CSV).
  • Top 2 Skills: Strong organizational and communication skills with high attention to detail; ability to collaborate effectively across cross-functional teams and multiple organizational levels. Proficiency with Microsoft Office (Word, Excel, PowerPoint, Outlook).

What will give you a competitive edge (preferred qualifications):
  • Experience in materials management within USDA, FDA, or EMA regulated environments. Demonstrated success leading cross-functional teams or projects. Experience with SAP, JMP, and Veeva Vault systems. Working knowledge of VICH, USDA, and/or EU GMP regulations for veterinary biologics.

Additional Information:
  • Location: Elwood, Kansas (Onsite).
  • Day shift position. Weekend or evening work may occasionally be required to support operations.
  • Minimal travel required (<5%).
  • Full-time, permanent, salaried position.

Don't meet every single requirement?
Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco, we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:
  • Multiple relocation packages for eligible roles
  • 8-week parental leave
  • 9 Employee Resource Groups
  • Annual bonus offering
  • Up to 6% 401K matching

Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job-related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.

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