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Method Validation Jobs in Wisconsin (NOW HIRING)

Method Development Scientist - III (Madison, Wisconsin) Work schedule : Monday - Friday (Day Shift ... Supports troubleshooting across development, validation, and sample analysis. * Maintains complete ...

... Assist with method validation, process improvements, and implementation of new technologies or procedures. · Maintain laboratory equipment and coordinate calibration, maintenance, and ...

Data Reviewer

Verona, WI · On-site

$35 - $43/hr

Review method validation data for accuracy, integrity, and regulatory compliance. * Work with chemists to resolve deficiencies or questions about data and results. * Write reports in accordance with ...

... method validation, process improvements, and implementation of new technologies or procedures. • Maintain laboratory equipment and coordinate calibration, maintenance, and troubleshooting ...

The Quality Control Analyst conducts time-sensitive qPCR assays, handles raw material and finished product samples, supports method validation and development, and contributes to environmental and ...

... method validation, process improvements, and implementation of new technologies or procedures. • Maintain laboratory equipment and coordinate calibration, maintenance, and troubleshooting ...

Periodic analysis of known standards and/or samples relative to various areas of testing are employed both as a means of method validation and analytical proficiency. The results of the analyses are ...

Showing results 41-60

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.

Method Development Scientist III

Labcorp

Madison, WI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 days ago


Labcorp rating

6.6

Company rating: 6.6 out of 10

Based on 1,144 frontline employees who took The Breakroom Quiz

97th of 120 rated laboratories


Job description


Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world's most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you'll have the opportunity to do meaningful work, grow your career and make a real impact on people's health around the world. Together, we're improving health and improving lives.


Method Development Scientist - III (Madison, Wisconsin)

Work schedule: Monday - Friday (Day Shift)

Method Development Scientist - III

Job Responsibilities:

In this role, you will support the development, transfer, troubleshooting, and documentation of sensitive and reliable LC-MS/MS bioanalytical methods for the analysis of pharmaceuticals and related compounds in biological matrices. You will apply scientific principles, regulatory awareness, and hands-on laboratoryexpertiseto generate high-quality data and support internal and external communications while contributing to process improvements.

No significant remote work or travel and does include direct client interaction.

Essential Duties

  • Individual contributor role in a regulated lab environment.
  • Develops routine and complex analytical methods for quantitation of pharmaceuticals from biological matrices, applying troubleshooting and documentation practices.
  • Supports method development and method transfer activities, including method writing and associated laboratory work.
  • Supports troubleshooting across development, validation, and sample analysis.
  • Maintains complete,accurate, andtimelydocumentationin accordance withSOPs, GLP, and regulatory requirements.
  • Supports data-driven decision-making by communicating method performance, risks, and resource needs.
  • Serves as a technical resource within the group,assistingwith troubleshooting and training asappropriate.
  • Participates in client interactions and internal cross-functional collaborations.
  • Contributes to evaluation of departmental procedures and local process improvements.
  • Promotes a cohesive and collaborative team environment.

Minimum Requirements

  • Bachelor's degree (Chemistry, Biochemistry, etc.)

  • 5 years or more of analytical laboratory experience

  • 5 years or more of LC-MS/MS experience

  • GLP/GMP/GCP/SOP experience

  • 3 years or more Method Development experience

Preferred Requirements

  • Doctoral degree (Chemistry, Biochemistry, etc.)

  • With any lab experience

  • Bioanalytical experience

Additional Requirements

  • Demonstrated communication skills (external publications and presentations)

  • Client management experience

  • Proven ability to prioritize and manage time

  • Excellent attention to detail

Application Window: 8/6 thru 8/10/2026

Benefits:Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan.For more detailed information, pleaseclick here.


Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.


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