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Method Validation Jobs in Wisconsin (NOW HIRING)

Foxconn WI

Quality Engineer

Mount Pleasant, WI · On-site

$69K - $90K/yr

Lead process and test method validation activities Monitor supplier quality performance and coordinate corrective actions for supplier-related issues * Develop and maintain quality metrics dashboards ...

Foxconn WI

Quality Engineer

Mount Pleasant, WI

$60K - $65K/yr

Lead process and test method validation activities Monitor supplier quality performance and coordinate corrective actions for supplier-related issues * Develop and maintain quality metrics dashboards ...

Foxconn WI

Sr. Quality Engineer

Mount Pleasant, WI · On-site

$85K - $116K/yr

Lead process and test method validation activities Monitor supplier quality performance and coordinate corrective actions for supplier-related issues * Develop and maintain quality metrics dashboards ...

Foxconn WI

Quality Engineer

Mount Pleasant, WI · On-site

$69K - $90K/yr

Lead process and test method validation activities Monitor supplier quality performance and coordinate corrective actions for supplier-related issues * Develop and maintain quality metrics dashboards ...

Foxconn WI

Quality Engineer

Mount Pleasant, WI · On-site

Lead process and test method validation activities Monitor supplier quality performance and coordinate corrective actions for supplier-related issues * Develop and maintain quality metrics dashboards ...

Foxconn WI

Sr. Quality Engineer

Mount Pleasant, WI · On-site

$90 - $125/hr

Lead process and test method validation activities Monitor supplier quality performance and coordinate corrective actions for supplier-related issues * Develop and maintain quality metrics dashboards ...

Foxconn WI

Sr. Quality Engineer

Mount Pleasant, WI

$60K - $65K/yr

Lead process and test method validation activities Monitor supplier quality performance and coordinate corrective actions for supplier-related issues * Develop and maintain quality metrics dashboards ...

Hologic, Inc.

WI · On-site

$98 - $153/hr

Test method validation, root cause failure analysis, statistical methods, and design of experiments. Skills The role requires the ability to drive action according to Deming Cycle / PDCA principles.

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Method Validation information

See Wisconsin salary details

$22

$52

$78

How much do method validation jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for method 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 a method validation?

A Method Validation job involves assessing and verifying analytical methods to ensure they produce reliable, accurate, and reproducible results. Professionals in this role typically work in pharmaceutical, biotechnology, or chemical industries, following regulatory guidelines such as ICH, USP, or FDA requirements. Their responsibilities include designing validation protocols, performing experiments, analyzing data, and documenting results. Method validation ensures compliance with industry standards and guarantees product quality and safety.

What does a method validation do?

As a Method Validation professional, you will design, conduct, and document experiments to confirm that laboratory methods produce accurate and reproducible results under specified conditions. Typical daily tasks include preparing protocols, running validation samples, analyzing data, and preparing comprehensive validation reports for internal or regulatory review. You’ll work closely with scientists, quality assurance teams, and regulatory specialists to ensure compliance with industry standards. This collaborative environment provides opportunities to contribute to critical product development stages and to build expertise that supports career progression into quality management, regulatory affairs, or advanced analytical roles.

What are the key skills and qualifications needed for method validation?

To excel in Method Validation, a strong background in analytical chemistry, laboratory techniques, and scientific data analysis is typically required, often supported by a degree in chemistry, biochemistry, or a related field. Familiarity with validation protocols, industry regulations (such as GLP, GMP, or ISO standards), and analytical instrumentation (e.g., HPLC, GC, MS) is essential. Strong attention to detail, problem-solving skills, and effective collaboration and documentation abilities help professionals thrive in this position. These skills are vital to ensure that laboratory methods are reliable, regulatory-compliant, and suitable for their intended purposes.

What are the most commonly searched types of Method Validation jobs in Wisconsin?

The most popular types of Method Validation jobs in Wisconsin are:

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

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

What job categories do people searching Method Validation jobs in Wisconsin look for?

The top searched job categories for Method Validation jobs in Wisconsin are:

Method Validation jobs near you
Infographic showing various Method Validation job openings in Wisconsin as of August 2026, with employment types broken down into 92% Full Time, 5% Part Time, and 3% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote 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 16 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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