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Validation Manager Jobs in Wisconsin (NOW HIRING)

Medline

Validation Engineer

Hartland, WI

$73K - $110K/yr

Responsible for managing and or performing revalidation, engineering studies to evaluate new ... Validate new and revalidate as appropriate existing equipment used in OTC/Cosmetic and medical ...

Medline

Validation Engineer

Hartland, WI · On-site

$73K - $110K/yr

Responsible for managing and or performing revalidation, engineering studies to evaluate new ... Validate new and revalidate as appropriate existing equipment used in OTC/Cosmetic and medical ...

Medline

Validation Engineer

Hartland, WI

$73K - $110K/yr

Responsible for managing and or performing revalidation, engineering studies to evaluate new ... Validate new and revalidate as appropriate existing equipment used in OTC/Cosmetic and medical ...

Centraprise Corp

BMS Validation Engineer

Glendale, WI · On-site

BMS Validation Engineer Job Location: Glendale, WI - Onsite Job Type: Fulltime Must Have Technical ... Experience in Battery Management System (BMS) ECU development. * Experience with Tools - Embedded ...

CAI

Validation Engineer

Kenosha, WI · On-site

... Team Management - Plan and coordinate work - Direct small teams in document development and/or execution Qualifications and Experience - Bachelor's degree in a science or engineering field (or ...

CAI

Validation Engineer

Kenosha, WI · On-site

$72K - $80K/yr

... Team Management - Plan and coordinate work - Direct small teams in document development and/or execution Qualifications and Experience - Bachelor's degree in a science or engineering field (or ...

CAI

Senior Validation Engineer

Kenosha, WI · On-site

... Management - Support execution of design reviews, equipment shakedown, commissioning, FATs, IQ, OQ, and PQ activities - Coordinate with project contractors and equipment vendors to execute required ...

CAI

Senior Validation Engineer

Kenosha, WI · On-site

$87K - $94K/yr

... Management - Support execution of design reviews, equipment shakedown, commissioning, FATs, IQ, OQ, and PQ activities - Coordinate with project contractors and equipment vendors to execute required ...

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All JobsValidation Manager JobsValidation Manager Jobs in Wisconsin

Validation Manager information

See Wisconsin salary details

$47.9K

$106.4K

$162K

How much do validation manager jobs pay per year?

As of Jun 27, 2026, the average yearly pay for validation manager in Wisconsin is $106,401.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,200.00 and $133,200.00 per year, depending on experience, location, and employer.

How does a Validation Manager typically collaborate with other departments during project execution?

Validation Managers frequently work cross-functionally with quality assurance, manufacturing, engineering, and regulatory teams to ensure all systems and processes meet required standards. Effective collaboration involves coordinating validation protocols, sharing critical documentation, and communicating status updates to keep projects on track. A Validation Manager often leads meetings to align stakeholders, addresses compliance concerns, and resolves issues swiftly to prevent delays. Building strong relationships across departments is essential for smooth validation processes and successful project outcomes.

What is the role of a validation manager?

A validation manager oversees the process of ensuring that products, processes, or systems meet specified requirements and quality standards. They develop validation protocols, coordinate testing activities, and ensure compliance with industry regulations, often working with quality assurance teams and utilizing validation tools. Their role is critical in industries like pharmaceuticals, manufacturing, and healthcare to ensure safety and efficacy.

What job makes $10,000 a month without a degree?

A Validation Manager typically earns a salary that can reach or exceed $10,000 per month, especially with experience and industry expertise. This role involves overseeing validation processes in industries like pharmaceuticals or manufacturing, often requiring strong technical skills and certifications but not necessarily a college degree.

What jobs in the US pay 300,000 a year?

Validation Managers in industries such as pharmaceuticals, biotechnology, and manufacturing can earn salaries approaching or exceeding $300,000 annually, especially with extensive experience, advanced certifications, and leadership responsibilities. High-level roles in finance, law, and executive management also frequently reach or surpass this salary level. Compensation varies based on location, company size, and individual expertise.

What Is a Validation Manager?

A validation manager works in a manufacturing plant and oversees the proper operation of machinery and equipment. Your job duties include developing operational plans for the entire facility, identifying areas of process improvement, and scheduling periodic auditing reviews of the facility. The qualifications needed for a career as a validation manager include a bachelor’s degree in business, organizational theory, quality control, or a related field. You also need strong communication and computer skills and experience in a management position.

What are the key skills and qualifications needed to thrive as a Validation Manager, and why are they important?

To thrive as a Validation Manager, you need a strong background in quality assurance, regulatory compliance (such as FDA or EMA guidelines), and validation principles, usually supported by a degree in life sciences or engineering. Familiarity with validation protocols, risk management tools, and systems like GMP documentation platforms is essential. Leadership, attention to detail, and effective communication are crucial soft skills for managing teams and coordinating cross-functional projects. These skills and qualities ensure that products and processes consistently meet regulatory standards, reducing risks and ensuring compliance.

What jobs pay 500,000 a year in the US?

Validation Managers typically do not earn $500,000 annually; such high salaries are more common in executive roles like CEOs, CFOs, or specialized high-level professionals in finance, law, or technology. Senior executives and certain specialized roles with significant responsibilities and experience can reach or exceed this income level, often including bonuses and stock options. Compensation varies widely based on industry, company size, and geographic location.

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

AspectValidation ManagerQuality Assurance Specialist
CertificationsGxP, ISO, or industry-specific validation certificationsISO, Six Sigma, or QA-related certifications
Work EnvironmentRegulated industries like pharmaceuticals, biotech, or medical devicesManufacturing, software, or service industries
Primary FocusEnsuring validation processes for equipment, systems, and processes meet standardsMonitoring and improving overall quality processes and compliance

The Validation Manager primarily oversees validation activities to ensure compliance with industry standards, focusing on equipment and process validation. In contrast, the Quality Assurance Specialist concentrates on maintaining overall quality standards across products and services. Both roles are essential for compliance but differ in scope and responsibilities.

What are Validation Managers?

Validation Managers are professionals responsible for overseeing and managing the validation processes within an organization, particularly in industries like pharmaceuticals, biotechnology, and manufacturing. Their main role is to ensure that products, equipment, and processes meet regulatory standards and operate consistently as intended. They coordinate validation activities, develop protocols, lead teams, and ensure compliance with quality and safety regulations. Validation Managers play a critical role in maintaining product quality, reducing risks, and ensuring that all procedures meet industry and governmental standards.
More about Validation Manager jobs
What are the most commonly searched types of Validation jobs in Wisconsin? The most popular types of Validation jobs in Wisconsin are:
What are popular job titles related to Validation Manager jobs in Wisconsin? For Validation Manager jobs in Wisconsin, the most frequently searched job titles are:
What job categories do people searching Validation Manager jobs in Wisconsin look for? The top searched job categories for Validation Manager jobs in Wisconsin are:
What cities in Wisconsin are hiring for Validation Manager jobs? Cities in Wisconsin with the most Validation Manager job openings:
Validation Manager jobs near you
Infographic showing various Validation Manager job openings in Wisconsin as of June 2026, with employment types broken down into 4% As Needed, 68% Full Time, 11% Part Time, 4% Temporary, 11% Contract, and 2% Nights. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $106,401 per year, or $51.2 per hour.
Manager, Computer Systems Assurance and Validation

Manager, Computer Systems Assurance and Validation

Arrowhead Pharmaceuticals

Madison, WI

Full-time

Posted 12 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

The Manager, Computer Systems Assurance and Validation is a subject matter expert (SME) and project owner responsible for leading and executing computer system validation and assurance activities across the organization. The role drives a risk-based approach to validation through CSA principles and frameworks such as GAMP 5 to ensure GxP systems meet intended use while driving efficiency and compliance with applicable regulatory requirements (e.g., FDA 21 CFR Part 11, EU Annex 11). Acting as a key cross-functional contributor, this individual partners with Quality, IS, Manufacturing, Regulatory, Clinical, and other stakeholders to influence compliance strategy, lead validation initiatives, and actively contribute to the maturation of the company's quality system and validation frameworks. The Manager serves in both an execution and oversight capacity depending on project scope, including signatory responsibilities on validation deliverables, and serves as a key technical voice in shaping how the organization approaches validation in a regulated GxP environment.

This role is based onsite 5x a week in Pasadena, CA or Verona, WI.

Responsibilities

Compliance Strategy & SME Leadership

  • Collaborate with Quality Assurance and IS leaders to support the development and implementation of risk-based CSA/CSV strategies and frameworks (CSA, GAMP 5) ensuring alignment with global regulatory requirements and industry best practices.
  • Drive the adoption of CSA principles for validation projects, facilitating the shift from traditional CSV approaches toward risk-based methodologies that reduce unnecessary documentation while maintaining compliance.
  • Serve as subject matter expert (SME) on validation and compliance topics, advising internal stakeholders on best practices for software validation and assurance.
  • Maintain awareness of evolving regulatory expectations and support updates to company policies and procedures accordingly.
  • Partner with Quality and cross-functional teams to develop, refine, and mature validation processes, quality systems, and frameworks, ensuring they are scalable, audit-ready, and aligned with current and emerging regulatory expectations.

Validation & Assurance Activities

  • Partner with System Owners to own and execute the full validation lifecycle for GxP systems, including planning, risk assessment, testing, reporting, and periodic review, applying a risk-based approach throughout.
  • Execute and/or oversee validation activities depending on project scope and complexity, including serving as a signatory on validation deliverables where appropriate.
  • Author validation deliverables (e.g., system requirements, validation plans, URS, test scripts, traceability matrices, validation reports) in accordance with regulatory expectations and internal standards.
  • Apply risk-based testing strategies to optimize validation efforts and focus resources on areas of greatest compliance impact.
  • Lead ongoing system assurance activities including periodic reviews, change management, and system decommissioning.

Requirements

  • Bachelor's degree in Computer Science, Information Systems, Life Sciences, Engineering, or a related field.
  • 8+ years of experience in CSV/CSA within the pharmaceutical, biotechnology, or medical device industry.
  • Solid understanding of regulatory requirements (e.g., FDA 21 CFR Part 11, EU Annex 11, GAMP 5, ICH guidelines).
  • Demonstrated experience applying a risk-based approach to validation, including CSA principles and GAMP 5 frameworks.
  • Proven ability to lead validation projects and serve as a cross-functional SME and collaborative partner.
  • Strong communication, influence, and problem-solving skills; operates with a high degree of independence and a proactive, ownership-oriented mindset.

Preferred

  • Advanced degree in a relevant field.
  • Experience with validation of both pure software systems (e.g., SaaS, cloud-based applications) and equipment with embedded or integrated software components (e.g., lab instruments, manufacturing equipment).
  • Experience contributing to the development or improvement of quality processes, quality systems, SOPs, or validation frameworks in a regulated environment.
  • Experience working with Quality Management Systems (QMS) and electronic validation tools.
  • Experience supporting regulatory inspections and audits.
Wisconsin pay range
$110,000—$135,000 USD
California pay range
$130,000—$150,000 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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