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Contract Method Validation Jobs in Trevor, WI (NOW HIRING)

HTM Contract Manager

Burlington, WI · On-site

$47.50 - $71.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Monitors contracts change dates, initiates, and processes necessary amendments, obtain and validate rate increases, fee schedules, and reimbursement methodologies * Completes and coordinates the ...

HTM Contract Manager

Burlington, WI · Remote

$47.50 - $71.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Monitors contracts change dates, initiates, and processes necessary amendments, obtain and validate rate increases, fee schedules, and reimbursement methodologies * Completes and coordinates the ...

New

Job Title: Validation QA Analyst Job Duration: 6+ Months Contract role Address: Lake Forest Illinois USA 60045 Interview Method: Phone then In Person Must Haves: Additional Information All your ...

Quality Engineer - Validation

Buffalo Grove, IL · On-site

$73K - $95K/yr

... and contract manufacturing. Nemera's manufacturing sites are located in the US, France, Germany ... Identify and complete continuous improvement projects utilizing Six Sigma tools and methodologies.

... and contract manufacturing. Nemera's manufacturing sites are located in the US, France, Germany ... Identify and complete continuous improvement projects utilizing Six Sigma tools and methodologies.

MLT

Lake Geneva, WI · On-site

$55 - $60/hr

Contract Position Summary We are seeking a qualified and detail-oriented Medical Laboratory ... Participate in instrument evaluations, method validations, and implementation of new procedures ...

Audit CMOs, contract test laboratories and/or raw material suppliers. * Manage product complaints ... Experience with method development and method validations in a QC chemistry and microbiology cGMP ...

Audit CMOs, contract test laboratories and/or raw material suppliers. * Manage product complaints ... Experience with method development and method validations in a QC chemistry and microbiology cGMP ...

Audit CMOs, contract test laboratories and/or raw material suppliers. * Manage product complaints ... Experience with method development and method validations in a QC chemistry and microbiology cGMP ...

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Contract Method Validation information

See Trevor, WI salary details

$22

$51

$77

How much do contract method validation jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for contract method validation in Trevor, WI is $51.34, according to ZipRecruiter salary data. Most workers in this role earn between $38.94 and $62.40 per hour, depending on experience, location, and employer.

What is the difference between Contract Method Validation vs Analytical Method Validation?

AspectContract Method ValidationAnalytical Method Validation
PurposeValidates that a contracted method meets specific requirements for a particular project or clientEnsures an analytical method is accurate, reliable, and reproducible for testing purposes
ScopeTypically project-specific, focusing on methods used under contractual agreementsBroader, covering method development, validation, and routine testing
CredentialsOften requires validation expertise, GMP knowledge, and industry-specific certificationsRequires analytical chemistry knowledge, validation experience, and relevant certifications
Work EnvironmentPharmaceutical, biotech, or manufacturing settings with client-specific projectsLaboratories performing routine testing and method development in similar industries

Contract Method Validation focuses on validating methods for specific client projects, while Analytical Method Validation ensures the overall reliability of testing methods used routinely in laboratories. Both roles require similar credentials and work in related environments, but their scope and purpose differ.

Microbiology Validation Engineer

Tek Labs Inc

East Troy, WI • On-site

Other

Posted 6 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.