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Validation Jobs in Wisconsin (NOW HIRING)

CAI

Senior Validation Engineer

Madison, WI · On-site

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&Q activities in alignment with project ...

CAI

Senior Validation Engineer

Madison, WI

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&Q activities in alignment with project ...

Clarios

Senior Cell Validation Engineer

Milwaukee, WI · On-site

The Senior Cell Validation Engineer is responsible for planning, executing and maintaining validation activities at Clarios' Lithium Ion and Advanced Products Laboratory. The engineer will also ...

Deloitte

System Test and Validation Lead

Milwaukee, WI · On-site +1

Drive validation and compliance activities for complex GxP systems as a Senior Consultant, Regulatory, Risk, and Compliance. This role supports system validation strategy, audit readiness, CAPA ...

Deloitte

System Test and Validation Lead

Milwaukee, WI · On-site +1

Drive validation and compliance activities for complex GxP systems as a Senior Consultant, Regulatory, Risk, and Compliance. This role supports system validation strategy, audit readiness, CAPA ...

Deloitte

System Test and Validation Lead

Milwaukee, WI · On-site +1

Drive validation and compliance activities for complex GxP systems as a Senior Consultant, Regulatory, Risk, and Compliance. This role supports system validation strategy, audit readiness, CAPA ...

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Validation information

See Wisconsin salary details

$22

$52

$78

How much do validation jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for validation in Wisconsin is $52.48, according to ZipRecruiter salary data. Most workers in this role earn between $39.81 and $63.80 per hour, depending on experience, location, and employer.

What is the difference between Validation vs Quality Assurance?

AspectValidationQuality Assurance
PurposeEnsures products meet specifications and intended usePrevents defects through process improvements
FocusProduct-specific testing and verificationProcess and system quality control
ActivitiesDesign validation, process validation, equipment validationAudits, process reviews, standards compliance
TimingBefore product releaseThroughout production cycle

Validation focuses on confirming that a product or process meets specified requirements before release, while Quality Assurance emphasizes maintaining quality standards throughout the production process to prevent defects. Both roles are essential in industries like pharmaceuticals and manufacturing, but they serve different stages of quality management.

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

To thrive as a Validation Engineer, you need a solid background in engineering or life sciences, with expertise in quality assurance and regulatory compliance. Familiarity with validation protocols, statistical analysis tools, and industry standards such as GMP, FDA, or ISO guidelines is essential. Strong analytical thinking, attention to detail, and effective communication skills help you identify issues and collaborate across teams. These abilities ensure that products and processes meet strict safety and quality requirements, minimizing risks and ensuring regulatory approval.

What are some common challenges faced by professionals in validation roles, and how can they be overcome?

Professionals in validation roles often face challenges such as tight project timelines, evolving regulatory requirements, and the need for meticulous documentation. Balancing thoroughness with efficiency is crucial, as validation processes must be both comprehensive and timely to support product launches or regulatory submissions. Effective communication with cross-functional teams, proactive planning, and staying updated with industry standards can help overcome these challenges and ensure successful validation outcomes.

What is a validation job?

Validation jobs involve ensuring that products, processes, or systems meet specific requirements and function as intended. In industries like pharmaceuticals, biotechnology, and manufacturing, validation specialists test equipment, procedures, and software to guarantee quality and compliance with regulatory standards. These professionals document their findings and help identify areas for improvement, playing a key role in quality assurance. Validation jobs are essential for maintaining product safety, effectiveness, and meeting industry regulations.
What are the most commonly searched types of Validation jobs in Wisconsin? The most popular types of Validation jobs in Wisconsin are:
Validation jobs near you
Infographic showing various Validation job openings in Wisconsin as of August 2026, with employment types broken down into 61% Full Time, 11% Part Time, and 28% Contract. Highlights an 100% In-person job distribution, with an average salary of $109,164 per year, or $52.5 per hour.

Integration (Process Validation) Engineer

Vonco Products LLC

Trevor, WI • On-site

$70K - $85K/yr

Full-time

Re-posted 17 days ago

Job description

Description

Integration (Process Validation) Engineer

Medical Device Contract Manufacturer - Flexible Films & Packaging


Position Summary

The Integration (Process Validation) Engineer is responsible for leading and supporting process validation and manufacturing integration activities for medical device packaging, flexible film converting, and related manufacturing processes. This role ensures manufacturing processes are developed, validated, transferred, and maintained in compliance with FDA Quality System Regulation (21 CFR Part 820), ISO 13485, customer requirements, and internal quality standards.
 

The engineer will work cross-functionally with Operations, Quality, Design Engineering, and customers to support new product introductions, process improvements, equipment qualifications, and ongoing manufacturing validation activities.


Reporting Structure

Reports To: VP of Quality and Integration Engineering

Department: Integration Engineering


Essential Duties and Responsibilities

Develop and execute IQ, OQ, and PQ validation protocols and reports.

Lead validation activities for flexible film converting, RF welding, heat sealing, pouch manufacturing, printing, and labeling operations.

Perform process capability studies and statistical analysis to support validation activities.

Establish process windows, critical process parameters, and acceptance criteria.

Support new product introductions (NPI) from concept through commercial production.

Identify and implement process improvements focused on quality, efficiency, scrap reduction, and throughput.

Lead root cause investigations and corrective actions related to process performance.

Ensure compliance with FDA 21 CFR Part 820 / QMSR, ISO 13485, GMP requirements, and customer-specific quality requirements.

Support internal, customer, and regulatory audits.

Project Management & Customer Communication

Lead cross-functional project activities related to process validation, equipment implementation, and new product integration.

Develop and manage project timelines, deliverables, and validation schedules to support customer and internal milestones.

Coordinate activities between Engineering, Quality, Operations, Supply Chain, and customer teams to ensure successful project execution.

Serve as a primary technical point of contact for customers during new product introductions, validation activities, process transfers, and ongoing manufacturing support.

Communicate project status, technical risks, validation progress, and issue resolution plans to internal leadership and customers.

Facilitate customer meetings, technical reviews, and validation planning discussions.

Support quotation reviews and provide technical input related to manufacturability, process capability, and validation requirements.

Collaborate with customers to understand product requirements, critical-to-quality characteristics, and regulatory expectations.

Support customer visits, audits, factory acceptance activities, and production trials as needed.



Requirements

Required Qualifications

Bachelor's degree in Engineering or related technical field required.

3+ years of engineering experience in a regulated manufacturing environment.

Experience with process validation in regulated manufacturing.

Working knowledge of IQ/OQ/PQ methodologies, statistical analysis, root cause analysis tools, and risk management methodologies.

Knowledge of FDA 21 CFR Part 820 and ISO 13485 requirements.

Strong technical writing and documentation skills.

Preferred Qualifications

Experience in flexible films, medical packaging, or converting operations.

Experience with RF welding, heat sealing, extrusion, laminating, pouch manufacturing, or printing technologies.

Experience supporting customer audits and regulatory inspections.

Experience with EQMS systems.

Key Competencies

Strong analytical and problem-solving skills

Project management and organizational skills

Attention to detail and documentation accuracy

Effective communication and collaboration skills

Ability to manage multiple priorities in a fast-paced manufacturing environment

Customer-focused mindset

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