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Computer System Validation Jobs in Wichita, KS (NOW HIRING)

CAMP Systems

EHM Analyst

Wichita, KS · On-site

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 ...

Camp Systems International

EHM Analyst

Wichita, KS · On-site

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 ...

Camp

EHM Analyst

Wichita, KS · On-site

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 ...

BHC

Sr. CAD Survey Technician

Wichita, KS · On-site

Understands advanced CAD principles and techniques regarding scaling, geographic coordinate systems ... CST) * A valid drivers license must be maintained and insurable * Survey operations and survey ...

BHC

Lead CAD Survey Technician - Wichita

Wichita, KS · On-site

Understands advanced CAD principles and techniques regarding scaling, geographic coordinate systems ... CST) * A valid drivers license must be maintained and insurable * Survey operations and survey ...

ANCHOR FABRICATION KANSAS

RECEIVING ASSOCIATE

Wichita, KS · On-site

$15.25 - $18.25/hr

Matches purchase orders with packing slips, validates accuracy, prepares tags for labeling ... Receives purchase orders into the computer system * Undertakes other duties appropriate to the role ...

ANCHOR FABRICATION KANSAS

RECEIVING ASSOCIATE

Wichita, KS · On-site

$15.25 - $18.25/hr

Matches purchase orders with packing slips, validates accuracy, prepares tags for labeling ... Receives purchase orders into the computer system * Undertakes other duties appropriate to the role ...

Papa John's

Assistant Manager

Wichita, KS

$15/hr

Must have valid driver's license and good driving record. Essential Physical Requirements: (Some ... computer system and POS register system Ability to communicate with associates and guests Ability ...

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Computer System Validation information

See Wichita, KS salary details

$10

$53

$84

How much do computer system validation jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for computer system validation in Wichita, KS is $53.62, according to ZipRecruiter salary data. Most workers in this role earn between $41.30 and $63.61 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 popular job titles related to Computer System Validation jobs in Wichita, KS?

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

What job categories do people searching Computer System Validation jobs in Wichita, KS look for?

The top searched job categories for Computer System Validation jobs in Wichita, KS are:

Computer System Validation jobs near you
Infographic showing various Computer System Validation job openings in Wichita, KS as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, 1% Temporary, and 2% Contract. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $111,526 per year, or $53.6 per hour.

Validation (CSA/CSV) Consultant

Arc Technologies Group

Wichita, KS • On-site

Full-time

Medical, Dental, Vision, Retirement

Re-posted 4 days ago

Job description

Job Title: Validation (CSA/CSV) Consultant
Location: Wichita, KS
Job Type: Full-Time
Experience Level: 1-8+ Years
Job Summary: We are seeking an experienced, motivated, and detail-oriented Validation Consultant to join our on-site team in Wichita. The Validation Consultant is responsible for planning, executing, and documenting validation and qualification activities for computerized systems, laboratory systems, manufacturing systems, infrastructure, and regulated processes within life sciences environments. This role works closely with Quality, IT, Engineering, Manufacturing, and business stakeholders to ensure systems are implemented and maintained in compliance with applicable regulatory requirements, including FDA 21 CFR Part 11, GxP, GAMP 5, and other global regulatory standards. The Validation Consultant provides technical and compliance expertise throughout the system lifecycle, from requirements gathering and risk assessment through testing, deployment, and ongoing change management.

If you consider yourself a motivated and ambitious individual, this will be the job for you.

Arc Technologies Group serves companies from growth startups to the Fortune 50 within Life Sciences and Healthcare.
Key Responsibilities:
  • Work on-site at ATG offices or Client offices or facilities on a daily basis
    • ​This may involve a commute of up to 70 miles for extended periods of time
  • Lead validation and qualification activities for computerized systems, applications, equipment, and infrastructure supporting regulated operations.
  • Develop and execute validation lifecycle deliverables including Validation Plans, User Requirements Specifications (URS), Functional Specifications, Risk Assessments, IQ/OQ/PQ protocols, Traceability Matrices, and Validation Summary Reports.
  • Apply risk-based validation methodologies consistent with GAMP 5, FDA Computer Software Assurance (CSA), and industry best practices.
  • Facilitate requirements gathering sessions with business, quality, engineering, laboratory, and IT stakeholders.
  • Review system design documentation to ensure compliance, data integrity, and validation requirements are appropriately addressed.
  • Author, review, and execute validation test protocols and document test results, deviations, investigations, and corrective actions.
  • Support implementation and validation of enterprise and manufacturing technologies, including MES, LIMS, ELN, ERP, SCADA, historian, automation, and laboratory systems.
  • Assess and document system impacts related to change controls, software updates, infrastructure modifications, and periodic reviews.
  • Support regulatory inspections, internal audits, client audits, and quality assurance reviews by providing validation documentation and compliance evidence.
  • Collaborate with project teams to develop validation strategies, schedules, and resource plans.
  • Ensure compliance with applicable regulations and standards including FDA, EU GMP Annex 11, GAMP 5, WHO, MHRA, and other relevant guidance. Ensure software and computer systems meet quality, safety, and regulatory standards.
  • Identify validation risks and develop mitigation strategies to support successful project delivery.
  • Participate in client-facing meetings, workshops, assessments, and strategic consulting engagements.
  • Understand and develop (SDLC) system/software development lifecycle and technical validation documentation. Execute validation testing where appropriate for IT and OT systems.
  • Produce or maintain accurate and up-to-date documentation for all IT and OT systems, including user manuals, standard operating procedures, work instructions, and validation protocols.
  • Provide advice/consultation on validation documentation and system/user requirements to achieve the best possible testing outcomes.
  • Think critically on test structures/design and ensure all client requirements are verified during validation.
  • Have attention to detail and apply patience when producing or reviewing documentation to identify and fix errors.
  • Put complex information into clear, concise, and accessible content/format for the intended audience. Ability to review, edit and proofread content for accuracy, clarity, and consistency.
  • Research and gather information on systems/projects to fully understand operational function and use case. Includes working with SMEs and other teams to research and collect information needed for accurate documentation.
  • Determine and analyze the needs of end users to ensure that all documentation and requirements are clear and tailored to the system.
  • Learn and understand complex systems and topics quickly.
  • Perform risk assessments on various systems
Above amp; Beyond Responsibilities:
  • Understand client requirements, business objectives amp; processes, in addition to their technology and systems
  • Leverage your sales mindset to deepen customer relationships, help transform services into comprehensive solutions, and collaborate with the sales team to align goals with outcomes
  • Identify expansion opportunities to drive growth and ensure customer satisfaction through innovative IT/OT, validation, engineering, and quality strategies
  • Support new technology implementation and provide assistance with technical issues, strategic direction, and financial analysis of projects/initiatives
  • Perform critical analysis of existing “People, Process, and Technology” state of clients
  • Work collaboratively with cross-functional teams, including R amp;D, quality assurance, and manufacturing, to deliver IT/OT solutions that meet business needs

Minimum Qualifications:
  • Bachelor's degree in Engineering, Computer Science, Information Technology, Life Sciences, or a related technical discipline.
  • Minimum of 2 years of experience in computerized systems validation (CSV), computer software assurance (CSA), commissioning and qualification (C amp;Q), or a related validation discipline within the pharmaceutical, biotechnology, medical device, or regulated healthcare industry.
  • Strong understanding of FDA 21 CFR Part 11, GxP regulations, data integrity principles, and GAMP 5 guidance.
  • Experience developing and executing validation lifecycle documentation including URS, risk assessments, IQ/OQ/PQ protocols, traceability matrices, and validation reports.
  • Experience supporting validation of GxP systems such as LIMS, MES, ERP, QMS, laboratory instruments, manufacturing execution systems, automation platforms, or cloud-based applications.
  • Knowledge of software development lifecycle (SDLC), change management, configuration management, and quality management processes.
  • Demonstrated ability to interpret regulatory requirements and translate them into practical validation strategies.
  • Strong technical writing, documentation, analytical, and problem-solving skills.
  • Excellent verbal and written communication skills with the ability to interact effectively with technical, quality, and business stakeholders.
  • Ability to manage multiple projects and priorities in a fast-paced consulting environment
  • Strong analytical and problem-solving skills, excellent communication and interpersonal skills, and the ability to work effectively in a team environment
  • Employees will be expected to commute up to 70 miles each way per day to various client sites if working at a long-term client facility. This is not a remote position
  • Employees must provide their own means of reliable transportation
  • BYOD is expected, employees will be required to use a cell phone for work purposes including the installation of work communication tools such as MS Teams or Outlook
  • Must be authorized to work in the United States.
  • Candidates must be authorized to be employed in the U.S. by any employer.
    • U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.
  • Must be available to work on-site in Wichita, KS during standard business hours (roughly 8am-5pm, Monday-Friday)
    • This position is not remote; reliable daily transportation to our Wichita office and/or customer sites is required.
  • Requires routine sitting, standing, walking, listening and talking
  • Acute mental and visual attention at all times
  • Ability to handle multiple projects while managing frequent interruptions
  • Requires moderate lifting or moving up to 100 pounds (lbs)
Experience with the follow items/areas are a plus but not required:
  • Experience with FDA Computer Software Assurance (CSA) methodology.
    Knowledge of manufacturing automation platforms, OT systems, and industrial control systems.
    Familiarity with cloud-hosted GxP systems and SaaS validation.
    Previous consulting experience supporting multiple clients and projects.
    Certifications such as ASQ Certified Quality Auditor (CQA), Certified Software Quality Engineer (CSQE), PMP, or relevant validation certifications.
    Experience supporting regulatory inspections and remediation initiatives.
  • Understand or have previous knowledge/experience in using document management systems and/or electronic execution systems with workflow and versioning capabilities.
  • Operational Technology foundational knowledge, including but not limited to experience with IIoT, PLCs, HMIs, SCADAs, etc.
  • Familiarity with enterprise IT and OT cybersecurity architecture and/or frameworks
  • Have the ability to troubleshoot hardware, software, and network problems amp; to think critically to analyze and remediate root causes
  • ITIL Framework
Who we are:
Arc Technologies Group is a boutique professional services firm focused exclusively on life sciences; including pharmaceutical manufacturing, biotech, CDMO, medical devices, and animal health. We deliver technology that actually works for organizations operating in highly regulated environments. Our team brings deep experience in IT/OT convergence, cybersecurity, digital transformation, and compliance-driven technology solutions across the entire life sciences technology space. We are proud to be an approved supplier in client's contingent workforce program and are committed to matching qualified professionals with meaningful contract opportunities at one of the world's leading pharmaceutical companies.
Benefits:
  • 401K
  • Short-term/Long-term disability
  • Medical/Dental/Vision may be available
  • Opportunities for professional development and career advancement
  • Collaborative amp; high-performance work environment
Arc Technologies Group employees are paid on an hourly basis; this is not a salaried position.
EEO amp; Employment Eligibility:
Arc Technologies Group, LLC is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability, or veteran status. ATG also complies with all applicable national, state, and local laws governing nondiscrimination in employment, as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.
ATG is an E-Verify employer. This position requires work authorization in the United States.

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