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Sr Validation Engineer Jobs in Wisconsin (NOW HIRING)

Senior Validation Engineer Location : Milwaukee, WI. Lead Projects. Inspire Teams. Build What Matters. We serve pharmaceutical companies across the United States, offering a vast array of services ...

New

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

Senior Validation Engineer

Madison, WI ยท On-site

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

WI ยท On-site

$110 - $140/hr

Position Summary We are seeking an experienced Senior Computer System Validation (CSV) Engineer to support validation activities for GMP-regulated manufacturing and automation systems at client. The ...

WI ยท On-site

$70 - $90/hr

Als Process & Validation Engineer speel je een sleutelrol in het ontwikkelen en valideren van ... of Senior Project Engineer, i.g.v. equipment / uitilities. * Je documenteert alle relevante ...

Work you'll do As a Senior Consultant, Regulatory, Risk, and Compliance on the Regulatory, Risk ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...

Work you'll do As a Senior Consultant, Regulatory, Risk, and Compliance on the Regulatory, Risk ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...

Work you'll do As a Senior Consultant, Regulatory, Risk, and Compliance on the Regulatory, Risk ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...

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Sr Validation Engineer information

See Wisconsin salary details

$35

$65

$99

How much do sr validation engineer jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for sr validation engineer in Wisconsin is $65.38, according to ZipRecruiter salary data. Most workers in this role earn between $52.16 and $74.23 per hour, depending on experience, location, and employer.

What is a Sr validation engineer?

Sr Validation Engineers are experienced professionals responsible for ensuring that products, systems, or processes meet regulatory standards and function as intended. They lead validation projects, develop protocols, oversee testing, and document results to confirm compliance with industry regulations, such as those from the FDA or ISO. Their work is essential in industries like pharmaceuticals, biotechnology, and manufacturing, where product quality and safety are critical. Senior validation engineers also mentor junior staff and help improve validation processes within their organizations.

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

To thrive as a Sr Validation Engineer, you need a solid background in engineering or life sciences, extensive experience with validation protocols, and a strong understanding of regulatory standards such as FDA, GMP, or ISO. Expertise in using validation software, risk assessment tools, and familiarity with documentation management systems is typically required, along with certifications like Six Sigma or ASQ CQE being advantageous. Exceptional problem-solving abilities, attention to detail, and effective communication skills help you lead teams and interact with cross-functional departments. These competencies are crucial for ensuring products and processes meet compliance standards, maintain quality, and support organizational success.

What are some common challenges a Sr validation engineer faces when managing multiple validation projects simultaneously?

A Sr Validation Engineer often manages several validation projects at once, which can present challenges such as coordinating timelines, ensuring compliance with regulatory standards, and balancing cross-functional communication. Keeping detailed documentation and staying organized are essential, as unexpected equipment issues or shifting project priorities may arise. Successful engineers proactively communicate with quality, manufacturing, and R&D teams to mitigate risks, maintain project momentum, and deliver results within required deadlines.

What is the difference between Sr Validation Engineer vs Validation Engineer?

AspectSr Validation EngineerValidation Engineer
Required CredentialsBachelor's/Master's in Engineering, certifications like CQE or ASQ, experience in validation processesBachelor's in Engineering or related field, some certifications preferred, less experience required
Work EnvironmentPharmaceutical, biotech, or manufacturing industries; leading validation projectsSupporting validation tasks under supervision, often in similar industries
Employer & Industry UsageUsed by companies requiring compliance with FDA, ISO, or GMP standardsCommonly used in manufacturing and quality assurance roles

The main difference between a Sr Validation Engineer and a Validation Engineer lies in experience, responsibility, and expertise. The Sr Validation Engineer typically leads validation projects, has more advanced certifications, and plays a strategic role in compliance. Validation Engineers support validation activities and often work under supervision. Both roles are essential in regulated industries like pharmaceuticals and manufacturing, but the senior role involves greater leadership and technical oversight.

What cities in Wisconsin are hiring for Sr Validation Engineer jobs?

Cities in Wisconsin with the most Sr Validation Engineer job openings:

Infographic showing various Sr Validation Engineer job openings in Wisconsin as of August 2026, with employment types broken down into 93% Full Time, 4% Part Time, and 3% Contract. Highlights an 85% Physical, 6% Hybrid, and 9% Remote job distribution, with an average salary of $135,986 per year, or $65.4 per hour.

Senior Validation Engineer

Gahagan & Bryant Associates, Inc.

Milwaukee, WI โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted yesterday

New


Job description

Job: Senior Validation Engineer
Location: Milwaukee, WI.
Lead Projects. Inspire Teams. Build What Matters.
We serve pharmaceutical companies across the United States, offering a vast array of services that assist companies with exceeding their goals and objectives. In today's world, it's never been more important to understand regulations and quality assurance activities as they relate to operations, vendors, engineering, construction and contractors. In 2020, Compli, LLC became a wholly owned subsidiary of George Butler Associates, Inc. This acquisition allowed Compli, LLC to become part of an integrated network of services where clients have more options to engage an impressive suite of in-house services.
Compli is a full service engineering contracting and consulting services company with a life sciences division specializing in pharma, biotech, API, Medical Device and laboratory facilities. Compli differentiates itself through an integrated approach to engineering, construction commissioning and validation.
Compli is a full service engineering contracting and consulting services company with a life sciences division specializing in pharma, biotech, API, Medical Device and laboratory facilities. We are seeking an experienced Senior/Project Lead Validation Engineer to join our growing team. Compli differentiates itself through an integrated approach to engineering, construction commissioning and validation.
Summary:
The Senior Validation Engineer is responsible for providing technical leadership and engineering expertise in the commissioning, qualification, and validation of facilities, utilities, equipment, systems, cleaning processes, and manufacturing processes within regulated life sciences environments.
What You'll Do:
  • Lead and support commissioning, qualification, and validation activities for facilities, utilities, equipment, systems, cleaning, and manufacturing processes.
  • Develop and execute commissioning and validation lifecycle documentation, including validation plans, protocols, test scripts, reports, and supporting documentation.
  • Develop project-specific commissioning, qualification, and validation strategies based on system requirements, risk, intended use, and regulatory expectations.
  • Provide technical leadership throughout all phases of projects, including greenfield construction, facility renovations, equipment installation, new product development, product launch, and process or system upgrades.
  • Lead and perform system, equipment, and process risk assessments and technical analyses.
  • Review engineering and system documentation to ensure alignment with validation requirements and regulatory expectations.
  • Develop, review, and execute applicable system lifecycle deliverables, including URS, SRS, FRS, DDS, RTM, FAT, SAT, IQ, OQ, PQ, and Final Validation Summary Reports.
  • Author and review validation and qualification protocols, technical reports, operating procedures, and other controlled documentation.
  • Investigate and resolve validation discrepancies, deviations, and technical issues using sound engineering judgment and practical problem-solving approaches.
  • Schedule and coordinate protocol execution with manufacturing, facilities, engineering, quality, project management, contractors, and other project stakeholders.
  • Manage multiple validation projects and priorities while meeting established project milestones and deadlines.
  • Provide technical guidance and mentorship to validation specialists, engineers, and other project team members as appropriate.
  • Serve as a technical resource and Subject Matter Expert (SME) in one or more areas of validation, qualification, or regulatory compliance.
  • Interface confidently and professionally with clients, contractors, management, regulatory and quality personnel, and project teams.
  • Support continuous improvement of validation practices, standards, templates, and execution strategies.
  • Other duties as assigned.
What You'll Bring:
  • Bachelor's degree in a related life sciences or requisite industry training and experience
  • 5 ๏ฟฝ 10 years GMP experience
  • Ability to converse about scientific matters
  • Ability to work independently or in collaboration with others
  • In depth understanding and application of validation principles, concepts, practices and standards
  • Considered a Subject Matter Expert (SME) in one area of validation
  • Proficient in current Good Manufacturing Practices and other applicable regulations
  • Experienced with all pertinent industry best practices (e.g., ISPE) including development and execution of all applicable system life cycle deliverables (e.g., URS, SRS, FRS, DDS, RTM, Unit, Integration, User Acceptance testing, FAT, SAT, Validation Planning, IQ, OQ, PQ, Final Validation Summary Report
  • Demonstrated expertise in at least one aspect of system qualification and regulatory compliance (e.g., EMEA, GCP, GLP, GMP, QSR) and internal requirements employing regulatory guidance and industry standards
  • Excellent written communication skills with emphasis in technical writing
  • Proficient in Microsoft Word, Excel, Power Point and Project
Physical Requirements & Work Environment
  • Ability to work on a computer for extended periods.
  • Ability to sit, stand, and walk project sites for prolonged periods.
  • Must be able to travel to job sites occasionally (minimum once per month).
Why You'll Love Working Here
At Compli, you'll work alongside talented professionals who share your passion for building great things. We offer a people-first culture and a comprehensive benefits package designed to support you personally and professionally, including:
  • Medical, dental, and vision insurance
  • Life, accident, and disability coverage
  • 401(k) with company match
  • Employee Assistance Program (EAP) and wellness initiatives
  • Paid company holidays, floating holidays, and flexible time off
  • Professional development and career advancement opportunities
Join Our Team
If you're ready to work on complex projects and build a career with impact, we'd love to hear from you.
Apply today and grow your future with Compli.
At GBA, we are an Equal Employment Opportunity Employer promoting diversity in our workforce by including all individuals regardless of age, race, religion, color, sex, national origin, marital status, genetic information, sexual orientation, gender identity, gender expression, disability, veteran status, pregnancy status, or any other status protected by law.