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System Validation Jobs in Madison, WI (NOW HIRING)

Sub-Zero, Inc.

Tooling Engineer

Madison, WI · On-site

... and system validation processes Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please ...

New

GENERAL BEVERAGE SALES CO

PURCHASING AGENT

Madison, WI · On-site

... systems Valid driver's license preferred, government issued id required Must pass a pre-employment drug screen Responsibilities Develop a strong knowledge of system inventory, customer orders ...

Abbott

Supervisor, Systems Verification

Madison, WI · On-site

$78K - $156K/yr

Write and execute system and software verification and validation tests. * Effectively record, reproduce, and communicate software and hardware bugs to development staff and contribute to their ...

Abbott

Supervisor, Systems Verification

Madison, WI · On-site

$78K - $156K/yr

Write and execute system and software verification and validation tests. * Effectively record, reproduce, and communicate software and hardware bugs to development staff and contribute to their ...

Johnson Controls

Security Service Technician

Madison, WI · On-site

$29.13 - $40.09/hr

Johnson Controls, a global leader in thermal management, mission-critical building systems, energy ... Valid driver's license with an excellent driving record. * High school diploma or GED (General ...

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System Validation information

See Madison, WI salary details

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How much do system validation jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for system validation in Madison, WI is $52.20, according to ZipRecruiter salary data. Most workers in this role earn between $39.23 and $64.90 per hour, depending on experience, location, and employer.

What is the difference between System Validation vs Quality Assurance Specialist?

AspectSystem ValidationQuality Assurance Specialist
CredentialsTypically requires engineering or technical degrees, certifications like ISTQB or ISO auditorRequires quality management certifications, such as ASQ CQE or Six Sigma
Work EnvironmentFocuses on testing and verifying systems, often in manufacturing, software, or medical device industriesInvolves process audits, documentation, and compliance across various industries
Employer & Industry UsageUsed in regulated industries like healthcare, aerospace, and software developmentCommon in manufacturing, software, and service industries for maintaining quality standards

System Validation and Quality Assurance Specialists both ensure product quality but differ in scope. System Validation primarily verifies that systems meet specifications, while Quality Assurance focuses on process improvement and compliance. Understanding these roles helps in choosing the right career path or hiring the right professional.

Is computer system validation a good field?

Computer system validation is a specialized field within quality assurance and regulatory compliance, primarily in industries like pharmaceuticals and biotech. It involves ensuring that computer systems meet regulatory standards through documentation, testing, and validation protocols, often requiring knowledge of GxP guidelines and validation tools. The field offers steady demand and opportunities for growth with relevant certifications and technical skills.

What is the job description of system validation?

System validation involves testing and verifying that a system or product meets specified requirements and functions correctly in its intended environment. It includes designing validation protocols, executing tests, analyzing results, and ensuring compliance with industry standards, often using tools like test management software. Professionals in this role need strong analytical skills and knowledge of quality assurance processes.
System Validation jobs near you
Infographic showing various System Validation job openings in Madison, WI as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, 2% Temporary, and 2% Contract. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $108,569 per year, or $52.2 per hour.

Engineer I, Quality Engineering (Analytical Method Validation)

Verona, WI • On-site

Arrowhead Pharmaceuticals
Pharmaceutical and Medicine Manufacturing • 201 - 500 employees
Learn more about Arrowhead Pharmaceuticalsexternal

$95K - $125K/yr

Full-time

Posted 25 days ago

Job description

Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.
The Position
This position within the Quality Assurance department will support ongoing programs for commercialization at Arrowhead. A key function of the position will involve providing leadership and guidance in principles of analytical method verification/validation in support of pre-clinical/clinical and commercialization activities at Arrowhead.
Generally, the position will support continued development and maintenance of quality systems supporting Good Manufacturing Practices (GMP) within the organization. Functions of this position will include serving as the Quality Assurance subject matter expert in method verification/validation, cross-functional interaction with internal departments to establish and/or update associated procedures/processes, review/approval of method validation documentation, performing validation assessment of changes and deviations for test methods used for GMP manufacturing.
Responsibilities
  • Serve as the Quality Assurance subject matter expert on method validation. This includes providing guidance, review, and/or approval of applicable validation strategy for analytical methods and supporting validation documentation. This position will also serve as a data reviewer, ensuring adherence to good documentation practices and data integrity.
  • Draft, review, and approve procedures in support of quality systems for qualification and validation.
  • Serve as a resource to mentor Quality Assurance members in Quality Engineering functions (e.g., department procedures, audits, method validation, validation assessments, etc.).
  • Work with cross-functional teams in the review and approval of internal and vendor-generated data/documentation in support of validation, qualification, and commissioning activities. Provide guidance on suitability of applicable equipment and assessment for use for validated method execution. Prepare documentation and provide support for internal and external audits.
  • Provide support for the issuance, review, tracking, and approval of internal deviations, change controls, and CAPAs as related to validation activities and assessments.
  • Support the development and implementation of periodic reviews for validated systems/processes including establishment of CPV procedures for commercial manufacturing.
  • Other duties, consistent with the position, as assigned.

Requirements
  • A bachelor's degree, or higher, in a science field.
  • Bachelor's degree with 8+ years of experience working within cGMP-regulated manufacturing, specifically in method validation-related roles in manufacturing and/or quality.
  • Working knowledge of GMP regulations (ICH Q2, ICH Q7, 21CFR Part 210/211, EU Annex 11/15, and 21CFR Part 11).
  • Excellent attention to detail and organizational skills.
  • Ability to multi-task and prioritize work tasks with minimal supervision.
  • Excellent interpersonal, verbal, and written communication skills
  • Competent knowledge and ability to use Microsoft Word and Excel.

Preferred
  • Prior experience with the use of an electronic document management system in a regulated environment is preferred.

Wisconsin pay range
$95,000-$125,000 USD
Arrowhead provides competitive salaries and an excellent benefit package.
Candidates must have current, valid authorization to work in the country where this role is located.
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