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Contract Cleaning Validation Engineer Jobs in Wisconsin

Compli

Senior Validation Engineer

Milwaukee, WI ยท On-site

Senior Validation Engineer Location : Milwaukee, WI. Lead Projects. Inspire Teams. Build What ... systems, cleaning processes, and manufacturing processes within regulated life sciences ...

New

Fujirebio Europe

WI ยท On-site

$70 - $90/hr

Als Process & Validation Engineer speel je een sleutelrol in het ontwikkelen en valideren van ... Je voert validatieactiviteiten uit (proces, product, cleaning, ...), stelt de nodige SOPs op en ...

Capgemini

WI ยท On-site

$79.93 - $125.60/hr

# Validation and Compliance Project Engineer | Life SciencesDiegemApply for this job* Permanent ... Experience with **aseptic processes, cleaning, disinfection, sterilisation**, or laboratory ...

Programmed Cleaning, Inc.

General Cleaner

Madison, WI

$14 - $16.75/hr

... a valid driver's license and reliable transportation are required. These locations are not ... From its origin as a local Milwaukee cleaning service, it has grown into a regional contract ...

Programmed Cleaning, Inc.

Lead Cleaner

Madison, WI ยท On-site

$19/hr

A valid driver's license is not required . * Employees will walk approximately half a block from ... From its origin as a local Milwaukee cleaning service, it has grown into a regional contract ...

Socket.dev

Senior Engineer, Quality Engineering

Verona, WI ยท On-site

$125 - $140/hr

... engineering, process design, risk assessments, and supporting validation documentation ... For cleaning and process validation, provide support in establishment of supporting documentation ...

New

Programmed Cleaning, Inc.

Project Worker

Madison, WI

$18.50/hr

Previous cleaning or floor-care experience is preferred. A valid driver's license is preferred but ... From its origin as a local Milwaukee cleaning service, it has grown into a regional contract ...

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Contract Cleaning Validation Engineer information

What is a contract cleaning validation engineer?

Contract Cleaning Validation Engineers are professionals who specialize in ensuring that cleaning procedures in manufacturing environments, especially in industries like pharmaceuticals and biotechnology, meet regulatory and quality standards. They are typically hired on a contract basis to validate and document that cleaning processes effectively remove contaminants and residues from equipment and facilities. Their work includes developing and executing cleaning validation protocols, analyzing test results, and preparing reports for regulatory compliance. These engineers play a crucial role in maintaining product safety and quality, and their expertise helps companies pass regulatory inspections. Contract Cleaning Validation Engineers often work with cross-functional teams and need strong knowledge of industry guidelines such as those from the FDA and EMA.

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

To thrive as a Contract Cleaning Validation Engineer, you need a strong background in chemical engineering, microbiology, or a related field, along with experience in cleaning validation within regulated industries. Familiarity with validation protocols, regulatory standards (such as FDA or EU GMP), and statistical analysis software is typically required. Attention to detail, problem-solving skills, and effective communication are crucial for documenting processes and collaborating with cross-functional teams. These skills ensure cleaning processes are compliant, reproducible, and safe, which is vital for product quality and regulatory approval.

What are some common challenges faced by a contract cleaning validation engineer during a project?

Contract Cleaning Validation Engineers often encounter challenges such as aligning cleaning protocols with both client requirements and regulatory standards, managing tight project timelines, and navigating complex equipment or facility layouts. Additionally, collaborating effectively with client teams and other contractors is crucial to ensure that validation documentation is accurate and comprehensive. Staying up-to-date with evolving industry regulations and best practices is also essential to delivering successful validation outcomes.

What is the difference between Contract Cleaning Validation Engineer vs Quality Assurance Specialist?

AspectContract Cleaning Validation EngineerQuality Assurance Specialist
CredentialsValidation certifications, engineering backgroundQA certifications, quality management training
Work EnvironmentPharmaceutical, biotech, or cleanroom facilitiesManufacturing, production, or laboratory settings
Employer & IndustryContract-based roles in regulated industriesIn-house or consulting roles in various industries
Search & Comparison IntentFocus on cleaning validation processesFocus on overall quality assurance practices

The Contract Cleaning Validation Engineer primarily specializes in validating cleaning processes within regulated environments like pharmaceuticals and biotech. In contrast, a Quality Assurance Specialist oversees broader quality systems, including audits and compliance. While both roles require understanding of industry standards, the validation engineer focuses on specific cleaning validation tasks, whereas the QA specialist manages overall quality assurance programs.

What are popular job titles related to Contract Cleaning Validation Engineer jobs in Wisconsin?

For Contract Cleaning Validation Engineer jobs in Wisconsin, the most frequently searched job titles are:

What job categories do people searching Contract Cleaning Validation Engineer jobs in Wisconsin look for?

The top searched job categories for Contract Cleaning Validation Engineer jobs in Wisconsin are:

What cities in Wisconsin are hiring for Contract Cleaning Validation Engineer jobs?

Cities in Wisconsin with the most Contract Cleaning Validation Engineer job openings:

Contract Cleaning Validation Engineer jobs near you
Infographic showing various Contract Cleaning Validation Engineer job openings in Wisconsin as of August 2026, with employment types broken down into 65% Full Time, 32% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution.

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.

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