ZipRecruiter

Log In

1

Computer System Validation Jobs in Madison, WI (NOW HIRING)

Abbott

Validation Associate III

Madison, WI · On-site

Author validation plans, validation protocols, and validation summary reports for computer system, processes, equipment, test methods, and cleaning processes. * Execute validation or qualification ...

Abbott Laboratories

Validation Associate III

Madison, WI · On-site

$80 - $100/hr

Author validation plans, validation protocols, and validation summary reports for computer system, processes, equipment, test methods, and cleaning processes. * Execute validation or qualification ...

Abbott

Validation Associate III

Madison, WI · On-site

Author validation plans, validation protocols, and validation summary reports for computer system, processes, equipment, test methods, and cleaning processes. * Execute validation or qualification ...

RXinsider LTD.

Validation Associate III

Madison, WI · On-site

$80 - $100/hr

Author validation plans, validation protocols, and validation summary reports for computer system, processes, equipment, test methods, and cleaning processes. * Execute validation or qualification ...

Azad Technology Partners

System Administrator

Oregon, WI · On-site

$60 - $80/hr

Bachelor's degree in computer science or a directly related technical discipline is preferred. * 3 ... Valid U.S. Driver's License is required. Preferred Skills * Ability to analyze technical issues and ...

CAI

Validation Engineer

Madison, WI

$72K - $80K/yr

Are You Ready? CAI is a professional services company established in 1996 that has grown to nearly 800 people worldwide. For mission-critical and regulated industries needing to deliver essential ...

CAI

Validation Engineer

Madison, WI · On-site

$72K - $80K/yr

Are You Ready? CAI is a professional services company established in 1996 that has grown to nearly 800 people worldwide. For mission-critical and regulated industries needing to deliver essential ...

next page

Showing results 1-20

All JobsComputer System Validation JobsComputer System Validation Jobs in Madison, WI

Computer System Validation information

See Madison, WI salary details

$10

$54

$86

How much do computer system validation jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for computer system validation in Madison, WI is $54.73, according to ZipRecruiter salary data. Most workers in this role earn between $42.16 and $64.90 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 that computer systems meet quality and compliance standards. It offers opportunities for professionals with skills in validation protocols, regulatory requirements, and tools like GxP and 21 CFR Part 11. The field provides steady employment, career growth, and the chance to work on critical quality assurance processes.

What are popular job titles related to Computer System Validation jobs in Madison, WI?

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

What job categories do people searching Computer System Validation jobs in Madison, WI look for?

The top searched job categories for Computer System Validation jobs in Madison, WI are:

Computer System Validation jobs near you
Infographic showing various Computer System Validation job openings in Madison, WI as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, and 4% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $113,861 per year, or $54.7 per hour.

GxP Laboratory Systems Administrator

Madison, WI • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

$100 - $125/hr

Other

Posted 8 days ago

Job description

Responsibilities
Business:

  • Support and system administration for identified applications

  • Investigate and resolve technical and business process issues

  • Communicate issues/resolutions with users and department managers

  • Escalate issues to application vendors as necessary

  • Troubleshoot and collaborate with end users and departmental managers

  • Maintain functional subject matter knowledge for assigned applications

  • Perform other duties as assigned


Regulatory:

  • Perform periodic application review and manage user access

  • Represent application documentation in client and regulatory audits

  • Contribute to audit finding responses

  • Contribute to CSV/CSA/computer system validation and software assurance projects, including application change control as required by GxP, policies, and SDLC

  • Draft CSV/CSA documentation (validation plans, design specs, traceability matrices, user requirements, test scripts, deviations, summary reports)


Information Systems/Informatics:

  • Coordinate communication between business and IS/Informatics

  • Triage escalation of technical issues

  • Update global systems inventory for applications

  • Coordinate releases into Development, Testing, and Production environments

  • Develop business scenarios to test applications

  • Verify installation and operation

  • Document analysis/testing for infrastructure changes (e.g., OS patches, major network changes)


Requirements

  • Bachelor’s in CS or life sciences (or related field) or equivalent experience

  • 4+ years administering/operating/maintaining LIMS, chromatography data systems, spectrophotometry systems, and related lab systems in a GxP environment

  • Advanced knowledge of computer programs (e.g., MS Word/Excel, data acquisition systems)

  • Ability to multi-task across projects and initiatives

  • Ability to deliver high-quality results under strict deadlines

  • Ability to work independently and with others


Preferred

  • Experience validating/supporting Agilent systems (Openlab, Chemstation, Cary UV)

  • Knowledge of GxP/CSV-CSA/21 CFR Part 11/EU Annex 11/SDLC

  • Experience with regulated asset management and environment monitor applications

  • Computer System Validation and GxP (21 CFR Part 11, Annex 11)

  • Pharmaceutical or CRO experience

  • Project Management certification


Benefits (if part of description)

  • Competitive salaries and an excellent benefit package

#J-18808-Ljbffr

Apply