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Computer System Validation Jobs in Kansas (NOW HIRING)

Execute re-qualification (RQ) studies and periodic reviews to ensure equipment, systems, and processes remain in a validated state. * Support and participate in change control processes for qualified ...

Recommend system improvements and validate new features. * Provide support to develop new product ... Excellent computer skills * Some travel may be required. Why Work at CAMP? Join a culture where ...

Recommend system improvements and validate new features. * Provide support to develop new product ... Excellent computer skills * Some travel may be required. Why Work at CAMP? Join a culture where ...

Recommend system improvements and validate new features. * Provide support to develop new product ... Excellent computer skills * Some travel may be required. Why Work at CAMP? Join a culture where ...

Audit reports, data, internal processes, computer system validations, facility, and procedures to support management to improve data integrity, reduce error rates, efficiency, and maintain compliance

Audit reports, data, internal processes, computer system validations, facility, and procedures to support management to improve data integrity, reduce error rates, efficiency, and maintain compliance

Senior Controls Engineer - Mission Critical

Lenexa, KS

$90K - $119K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Conduct system testing, validation, and troubleshooting during commissioning and operational phases ... Bachelor's degree in Electrical Engineering, Computer Engineering, Mechanical Engineering, or a ...

Senior Controls Engineer - Mission Critical

Lenexa, KS · On-site

$90K - $119K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Conduct system testing, validation, and troubleshooting during commissioning and operational phases ... Bachelor's degree in Electrical Engineering, Computer Engineering, Mechanical Engineering, or a ...

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Computer System Validation information

See Kansas salary details

$9

$48

$76

How much do computer system validation jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for computer system validation in Kansas is $48.44, according to ZipRecruiter salary data. Most workers in this role earn between $37.31 and $57.45 per hour, depending on experience, location, and employer.

What is a computer system validation?

A Computer System Validation (CSV) job involves ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, meet compliance and regulatory requirements. CSV professionals develop and execute validation protocols to confirm that software, hardware, and processes function as intended and maintain data integrity. They work with quality assurance, IT, and regulatory teams to document compliance with standards like FDA 21 CFR Part 11 and GxP. This role is critical in maintaining system reliability, product quality, and patient safety.

What are the key skills and qualifications needed to thrive in computer system validation, and why are they important?

To excel in Computer System Validation, candidates typically need a background in computer science, engineering, or life sciences, with expertise in validating software and systems in regulated environments such as pharmaceuticals or medical devices. Familiarity with tools like validation documentation software, GAMP 5 guidelines, FDA 21 CFR Part 11 regulations, and potentially certifications like CSV Professional or Six Sigma is highly valued. Strong attention to detail, analytical thinking, and effective communication skills help professionals work collaboratively and document findings precisely. These abilities ensure compliance, data integrity, and the reliability of computerized systems critical to safety and quality.

What are some typical challenges faced in computer system validation roles?

Professionals in Computer System Validation often encounter challenges such as keeping up with evolving regulatory requirements, ensuring complete and accurate documentation, and coordinating with cross-functional teams to implement validation protocols. Balancing thoroughness with project deadlines can also be demanding, as every validation step must stand up to external audits. However, these challenges provide valuable experience, strengthen project management abilities, and emphasize teamwork—key attributes that support career advancement into validation leadership or quality assurance roles.

Is computer system validation a good field?

Computer System Validation (CSV) is a vital part of regulated industries like pharmaceuticals and biotech, ensuring software and systems meet compliance standards such as GxP. It involves documentation, testing, and validation of computer systems, often requiring knowledge of regulatory requirements and validation tools. The field offers stable employment opportunities and career growth for professionals with technical skills and certifications like GAMP or 21 CFR Part 11 compliance.

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

The most popular types of Computer System Validation jobs in Kansas are:

What are popular job titles related to Computer System Validation jobs in Kansas?

For Computer System Validation jobs in Kansas, the most frequently searched job titles are:

What job categories do people searching Computer System Validation jobs in Kansas look for?

The top searched job categories for Computer System Validation jobs in Kansas are:

What cities in Kansas are hiring for Computer System Validation jobs?

Cities in Kansas with the most Computer System Validation job openings:

Infographic showing various Computer System Validation job openings in Kansas as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 12% Part Time, and 4% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $100,763 per year, or $48.4 per hour.

Validation Engineer

Pioneer Data Systems

Valley Falls, KS • On-site

Contractor

Re-posted 10 days ago


Job description

Job Description

Job Description:    POSITION SUMMARY
Validation engineer with experience in equipment, HVAC, utility and process qualification within a pharmaceutical industry. Previous plant experience is recommended. Background in aseptic processing, microbiology, environmental monitoring, chemistry, and production is recommended. The additional resources are requested for a total of fourteen (14) weeks starting in December 2017 and ending March 2018 to support Winter Shutdown changes. Hours can involve weekend or night shifts. Validation activities including writing system impact assessments, oversight of engineering during shutdown activities, execution of installation qualification, operational qualification, performance qualification, and summarizing qualification results/drafting qualification report summaries. The support staff must act in accordance with plant safety requirements, training and procedures.
POSITION RESPONSIBILITIES
Schedules and executes validations/qualifications per Standard Operating Procedures (SOPs) and regulatory guidelines.
Coordinates and communicates all testing with affected functional groups and evaluates test results.
Executes equipment, facility, utility and computer system, Automated Process Control validation studies to include protocol preparation, scheduling, protocol execution, analyze data and compose a final report.
Oversee and assist Engineers and/or Technicians with their assigned projects.
Provide technical expertise to define approaches and execution of system validation activities in accordance with cGMP, cGXP, CFR 21 Parts, 11, 210 and 211, EU Annex 11, ICH Q7, Q8 and Q9, and other applicable regulations, procedures and industry guidance.
Thorough understanding of risk based validation, industry standards and best practices for validation.
ORGANIZATIONAL RELATIONSHIPS
Will interact with Shutdown stakeholders: Engineering, Operations, Quality, Safety, Planning, Contractors, etc.
Weekly/daily meeting attendance as required.
Will participate in team led by Pfizer group leaders.
EDUCATION AND EXPERIENCE
Education: BS/BA degree in science, engineering, manufacturing technology or closely related field or combination of education and work experience
Experience: Recommended minimum of 4 years pharmaceutical validation experience
TECHNICAL SKILLS REQUIREMENTS
Knowledge of ICH and other regulatory guidelines; demonstrated ability to interpret and apply these guidelines to document writing
PHYSICAL POSITION REQUIREMENTS
Logistics: Requires contractor to be on-site weekly with travel home every other weekend
Must be able and willing to work beyond office hours which may include weekends.
Requires routine sitting, standing, walking, listening and talking
Acute mental and visual attention at all times
Handle multiple projects while managing frequent interruptions
Requires moderate lifting or moving up to 25 pounds (lbs

Additional Information

Anuj Mehta

732-947-3452