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Computer System Validation Jobs in Wisconsin (NOW HIRING)

WI · On-site

$110 - $140/hr

Position Summary We are seeking an experienced Senior Computer System Validation (CSV) Engineer to support validation activities for GMP-regulated manufacturing and automation systems at client. The ...

WI · On-site

$80 - $120/hr

As the Computer System Validation (CSV) Expert you will report directly to the local CSV manager and be the domain expert responsible for implementing Computer System Validations at our site in ...

New

Bachelor's degree in business, information systems, computer science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment ...

Bachelor's degree in business, information systems, computer science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment ...

Bachelor's degree in business, information systems, computer science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment ...

Oversee all Computer System Validation protocol approvals and executions. Scope of the Role * Quality Guardianship: Ensure that routine validation work and project design and commissioning integrate ...

New

Oversee all Computer System Validation protocol approvals and executions. Scope of the Role * Quality Guardianship: Ensure that routine validation work and project design and commissioning integrate ...

CSV Engineer

Mount Horeb, WI · On-site

$120K - $135K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Computer system validation methodologies * Strong technical writing skills with attention to detail. * Direct experience with Evolve System preferred. BENEFITS: What We Offer: Competitive ...

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Computer System Validation information

See Wisconsin salary details

$10

$54

$86

How much do computer system validation jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for computer system validation in Wisconsin is $54.83, according to ZipRecruiter salary data. Most workers in this role earn between $42.21 and $65.05 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 the most commonly searched types of Computer System Validation jobs in Wisconsin?

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

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

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

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

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

Infographic showing various Computer System Validation job openings in Wisconsin as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, and 3% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $114,039 per year, or $54.8 per hour.

Senior Computer System Validation (CSV) Engineer - Consultant

Inteldot

WI • On-site

$110 - $140/hr

Other

Posted 9 days ago


Job description

Position Summary

We are seeking an experienced Senior Computer System Validation (CSV) Engineer to support validation activities for GMP-regulated manufacturing and automation systems at client. The ideal candidate will have extensive experience validating computerized systems within the pharmaceutical or biotechnology industry and hands-on experience with Emerson DeltaV automation systems. The successful candidate will work closely with Engineering, Automation, Manufacturing, Quality Assurance, and IT teams to ensure computerized systems are validated and maintained in compliance with FDA regulations, GAMP 5, and 21 CFR Part 11 requirements.

Location: Texas (Onsite)

Administrative shiftResponsibilities
  • Lead Computer System Validation (CSV) activities for GMP computerized systems.
  • Develop, review, and execute validation documentation, including Validation Plans, Risk Assessments, IQ/OQ/PQ protocols, Traceability Matrices, and Summary Reports.
  • Validate automation systems, including Emerson DeltaV DCS, SCADA, and supporting infrastructure.
  • Support commissioning and qualification activities for new and existing manufacturing systems.
  • Perform impact assessments, change control evaluations, and periodic reviews.
  • Ensure compliance with FDA, cGMP, GAMP 5, ALCOA+, and 21 CFR Part 11 requirements.
  • Collaborate with Automation, Engineering, IT, Manufacturing, and Quality teams during project execution.
  • Support audits and regulatory inspections by providing validation documentation and technical expertise.
  • Review system lifecycle documentation and maintain validated system status.
Required Qualifications
  • Bachelor’s degree in engineering, Computer Science, Information Systems, or related technical discipline.
  • 5+ years of Computer System Validation experience in the pharmaceutical, biotechnology, or medical device industry.
  • Hands-on experience validating Emerson DeltaV systems is required.
  • Strong understanding of GAMP 5, FDA regulations, cGMP, and 21 CFR Part 11.
  • Experience developing and executing IQ, OQ, and PQ protocols.
  • Experience with change control, deviation investigations, CAPA, and risk assessments.
  • Excellent technical writing and documentation skills.
  • Strong communication and cross-functional collaboration skills.
Preferred Qualifications
  • Experience with Manufacturing Execution Systems (MES), SCADA, PLCs, or process automation systems.
  • Knowledge of electronic batch records (EBR) and manufacturing systems integration.
  • Experience supporting commissioning, qualification, and validation (CQV) projects in biologics or sterile manufacturing environments.
Technical Skills
  • Emerson DeltaV (Required)
  • Computer System Validation (CSV)
  • GAMP 5
  • 21 CFR Part 11
  • cGMP/FDA Compliance
  • IQ/OQ/PQ Protocols
  • Risk Assessments
  • Change Control
  • CAPA
  • Commissioning & Qualification (CQV)
  • Automation Systems Validation
  • Technical Documentation
Preferred Industry Experience
  • Biotechnology
  • Pharmaceutical Manufacturing
  • GMP-Regulated Facilities
  • Cell & Gene Therapy or Biologics Manufacturing (preferred)
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