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Method Validation Jobs in Wisconsin (NOW HIRING)

Lead the validation of rapid microbiological methods, including the NeoGen system, to ensure reliability and regulatory compliance. * Perform method suitability testing across multiple product ...

Validation Engineer

Hartland, WI · On-site

$73K - $110K/yr

... test method validations of applicable products. * Validate new and revalidate as appropriate ... existing equipment used in OTC/Cosmetic and medical device manufacturing. * Perform engineering ...

Validation Engineer

Hartland, WI · On-site

$73K - $110K/yr

... test method validations of applicable products. * Validate new and revalidate as appropriate ... existing equipment used in OTC/Cosmetic and medical device manufacturing. * Perform engineering ...

Validation Engineer

Hartland, WI · On-site

$73K - $110K/yr

... method validations of applicable products. Validate new and revalidate as appropriate existing ... equipment used in OTC/Cosmetic and medical device manufacturing. Perform engineering studies to ...

Validation Engineer

Hartland, WI · On-site

$73K - $110K/yr

... test method validations of applicable products. * Validate new and revalidate as appropriate ... existing equipment used in OTC/Cosmetic and medical device manufacturing. * Perform engineering ...

... test method validations of applicable products. * Validate new and revalidate as appropriate ... existing equipment used in OTC/Cosmetic and medical device manufacturing. * Perform engineering ...

Senior Validation Quality Engineer

Sturtevant, WI · On-site

$85K - $116K/yr

Oversee the operation of the Quality System process related to product, process, and/or test method Validation and Re-Validation. Oversee the Installation, Operational and Performance Qualification ...

Senior Validation Quality Engineer

Sturtevant, WI · On-site

$85K - $116K/yr

Oversee the operation of the Quality System process related to product, process, and/or test method Validation and Re-Validation. Oversee the Installation, Operational and Performance Qualification ...

Lead the validation of rapid microbiological methods, including the NeoGen system, to ensure reliability and regulatory compliance. * Perform method suitability testing across multiple product ...

You will also be involved in new method development and Validation. You will also support the training of fellow team members on instrumentation and test methods. Your impact will be as a key team ...

The Performance Validation Engineer is responsible for developing, implementing, maintaining, and ... This role applies Lean Manufacturing principles, methodologies, and tools to drive operational ...

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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 Aug 16, 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 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 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 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:

Infographic showing various Method Validation job openings in Wisconsin as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 7% Part Time, 1% Temporary, and 6% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $109,164 per year, or $52.5 per hour.

Microbiology Validation Engineer

Tek Labs Inc

East Troy, WI • On-site

Other

Posted 5 days ago


Job description

Title: Microbiology Validation Engineer
Location: East Troy, WI (Onsite)
Duration: 6-Month Contract (Opportunity to Renew)

Key Requirements:

  • Bachelor’s degree in Microbiology, Biology, Chemistry, or related scientific field with 3–7+ years of pharmaceutical or biotechnology validation experience.
  • Strong hands-on experience with microbiological method validation, including protocol development, execution, documentation, and comparative testing in a cGMP-regulated environment.
  • Experience with USP microbiological methods, rapid microbiological systems, method suitability studies, risk assessments, deviation investigations, and validation reporting.
  • Working knowledge of 21 CFR Parts 210/211, Data Integrity, process validation, IQ/OQ activities, and pharmaceutical laboratory compliance requirements.