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Validation Scientist Jobs in Wisconsin (NOW HIRING)

Experience Required Academic Experience Required Bachelor's Degree in Engineering, Chemistry, Microbiology, or related field or equivalent work experience in a validation scientist role Operational ...

Experience Required Academic Experience Required Bachelor's Degree in Engineering, Chemistry, Microbiology, or related field or equivalent work experience in a validation scientist role. Operational ...

Validation Engineer

Hartland, WI · On-site

$73K - $110K/yr

REQUIRED EXPERIENCE Education Bachelor of Science Degree in Biology, Chemistry, or Engineering. Work Experience At least 2 years of validation experience in a cGMP Device or Drug environment.

Validation Engineer

Hartland, WI · On-site

$73K - $110K/yr

Bachelor of Science Degree in Biology, Chemistry, or Engineering. Work Experience * At least 2 years of validation experience in a cGMP Device or Drug environment. * Experience with validations of ...

Bachelor of Science Degree in Biology, Chemistry, or Engineering. Work Experience * At least 2 years of validation experience in a cGMP Device or Drug environment. * Experience with validations of ...

Validation Engineer

Hartland, WI · On-site

$73K - $110K/yr

Bachelor of Science Degree in Biology, Chemistry, or Engineering. Work Experience * At least 2 years of validation experience in a cGMP Device or Drug environment. * Experience with validations of ...

Validation Engineer

Hartland, WI · On-site

$73K - $110K/yr

Bachelor of Science Degree in Biology, Chemistry, or Engineering. Work Experience * At least 2 years of validation experience in a cGMP Device or Drug environment. * Experience with validations of ...

WI · On-site

$73 - $110/hr

Bachelor of Science Degree in Biology, Chemistry, or Engineering.**Work Experience*** At least 2 years of validation experience in a cGMP Device or Drug environment.* Experience with validations of ...

Senior Validation Engineer Location : Milwaukee, WI. Lead Projects. Inspire Teams. Build What ... Ability to converse about scientific matters * Ability to work independently or in collaboration ...

New

WI · On-site

$79.93 - $125.60/hr

# Validation and Compliance Project Engineer | Life SciencesDiegemApply for this job* Permanent ... scientists, and architects to help the world's most innovative companies unleash their potential.

Validation Engineer II

Sturgeon Bay, WI · On-site

$83K - $105K/yr

Bachelor's in Engineering, Life Sciences, or related field. * 3+ years' experience in validation or quality in a regulated industry. * Knowledge of FDA, ISO 13485, 21 CFR Part 820 standards.

... in a science or engineering field (or equivalent experience) - 2-4 years' experience in commissioning and qualification in a regulated industry - Familiarity with ISPE Baseline Guide 5 (Second ...

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Validation Scientist information

See Wisconsin salary details

$22

$52

$78

How much do validation scientist jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for validation scientist 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 validation scientist?

Validation Scientists are professionals responsible for ensuring that processes, equipment, and systems in industries like pharmaceuticals, biotechnology, and manufacturing meet regulatory and quality standards. They design and execute validation protocols to confirm that products are consistently produced and controlled according to set specifications. Their work is critical for maintaining product safety, efficacy, and compliance with industry regulations. Validation Scientists often collaborate with quality assurance, engineering, and production teams to troubleshoot issues and implement improvements.

What are the key skills and qualifications needed to thrive as a validation scientist?

To thrive as a Validation Scientist, you need a strong background in life sciences or engineering, with knowledge of regulatory standards like GMP and experience in method or process validation. Familiarity with validation software, data analysis tools, and documentation systems is typically required, along with certifications such as Six Sigma or ASQ CQA being advantageous. Attention to detail, problem-solving abilities, and effective communication are standout soft skills in this role. These competencies are crucial for ensuring compliance, product quality, and successful audits in highly regulated environments.

What are some common challenges faced by validation scientists when working on new product launches?

Validation Scientists often encounter challenges such as tight project timelines, evolving regulatory requirements, and the need to coordinate with multiple departments including R&D, Quality Assurance, and Manufacturing. Managing documentation and ensuring all validation protocols and reports meet industry standards can also be demanding, especially in highly regulated environments like pharmaceuticals or biotechnology. Successful Validation Scientists develop strong project management and communication skills to navigate these complexities and ensure smooth product launches.

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

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

Infographic showing various Validation Scientist job openings in Wisconsin as of August 2026, with employment types broken down into 1% As Needed, 90% Full Time, 5% Part Time, and 4% Contract. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution, with an average salary of $109,164 per year, or $52.5 per hour.

Associate Validation Scientist

Perrigo Company plc

Eau Claire, WI • On-site

Full-time

Re-posted 5 days ago


Perrigo rating

8.5

Company rating: 8.5 out of 10

Based on 56 frontline employees who took The Breakroom Quiz

18th of 86 rated pharmaceutical


Job description

At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill, Compeed, Solpadeine, NiQuitin, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.

Join us on our One Perrigo journey as we evolve to win in self-care.

Description Overview

Prepare and maintain validation protocols and validation standard operating procedures for Perrigo Infant Formula operations.  Duties include development, execution, documentation, and monitoring manufacturing validation projects.   Investigate the manufacturing and production processes and prepare corrective actions and/or revalidation studies.  Coordinate with personnel from the other departments, such as Quality Assurance, Production, Technical, and Engineering to successfully execute and document the results of the validation projects or routine programs.  Perform/manage annual CCP and OPRP testing as well as the annual cleaning verifications.  Oversee all Computer System Validation protocol approvals and executions.

Scope of the Role
  • Quality Guardianship:   Ensure that routine validation work and project design and commissioning integrate the relevant Perrigo standards and relevant regulatory standards.  Prepare validation studies and protocols final reports, on a timely basis. Validation scope includes, but is not necessarily limited to: process vessels, cleaning/sanitization, product and process line sterilization, automated/electronic control systems, manufacturing processes.  Plan and execute multiple assigned validation activities simultaneously, which may include use of PCs monitoring, laboratory work environment as well as significant projects for new lines, new products process/facility/equipment modifications or process improvements. Support HACCP study, process flow and QMS reviews.  Assist in the HACCP study completion on a timely basis.  
     
  • Quality Control Activities:   Supports projects as Validation/Food Safety/Quality representative.  Supports HACCP for the implementation and management of relevant food safety control measures. Prepare and maintain QA/Validation standard operating procedures. Develop and maintain compliance with Validation Master Plans.  Follow Good Manufacturing Practices; report food safety and quality issues immediately.
     
  • People and Know-How:  For validation programs, develop the required training material, train and coach on the required elements to ensure that production will take place achieving the objectives defined for food safety and quality. Drive the development of competence of operators and promote quality awareness and commitment.
     
  • Quality Auditing and Verification:  Perform annual verification activities, including CIP and CCP/OPRP verifications.  Support readiness for internal and external audits.  Support Management of Change (MOC) as needed.  Maintain compliance with regulations and refer to the Quality Management System on all related procedures and programs. Understand the food safety and quality aspects of the position. 
     
  • Quality Mastership:   Support Continuous Improvement initiatives in the quest for zero defect.  Support activities to achieve compliance with the Quality Management System requirements and other applicable instructions and standards.  Identify non-conformance issues and coordinate Quality/Food Safety risk analysis. 
     
  • Performs other duties as assigned.
Experience Required

Academic Experience Required
Bachelor's Degree in Engineering, Chemistry, Microbiology, or related field or equivalent work experience in a validation scientist role

Operational Experience 

  • Experience with validation responsibilities in food, pharmaceutical, or medical device field
  • Minimum of 3-5 years of related Quality experience
  • Experience in regulated food manufacturing environment with exposure to 21 CFR 117, lean manufacturing, FSSC22000/SQF regulations and preferred experience with 21 CFR 106/107 and 21 CFR 113.

SKILLS:

  • Leadership and people development skills
  • Local language and English language written and spoken
  • Excellent written and oral communication skills, including report writing
  • Ability to work independently and handle multiple priorities 
  • Proficiency with PCs and software such as Access; Excel; Word; PowerPoint; 
  • Technical writing ability in an FDA regulated industry and ability to translate technical / quality / compliance theory into practical application
  • Demonstrated ability to lead projects and teams 
  • Working knowledge of production processes and equipment
  • Analytical and problem solving skills
  • Working knowledge of instrumentation and data collection

Benefits
We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.

Find out more about Total Rewards at Perrigo.

We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here

Applicants please note: To apply to this position please click the APPLY button at the bottom of the application.  (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.

We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.  #weareperrigo


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