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Cleaning Validation Jobs (NOW HIRING)

Moriah Engineering

PR · On-site

The Cleaning Validation Specialist will be responsible for developing, executing, and managing cleaning validation activities to ensure compliance with regulatory requirements and internal quality ...

MedPharm

Cleaning Validation Engineer

Durham, NC · On-site

Position Summary - The Cleaning Validation Engineer oversees the development, maintenance, and governance of MedPharm's site-wide cleaning validation program across the full product lifecycle, from ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

The ideal candidate will have strong experience in cleaning validation, including disinfectant and sanitization validation for Microbiology QC Laboratories and manufacturing areas, ensuring ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

The ideal candidate will have strong experience in cleaning validation, including disinfectant and sanitization validation for Microbiology QC Laboratories and manufacturing areas, ensuring ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

The ideal candidate will have strong experience in cleaning validation, including disinfectant and sanitization validation for Microbiology QC Laboratories and manufacturing areas, ensuring ...

PSC Biotech

Cleaning Validation Engineer

Minneapolis, MN · On-site

$90K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Your Role The Cleaning Validation Engineer is responsible for the development, modification, execution, and reporting of cleaning validation activities supporting biopharmaceutical manufacturing ...

PSC Biotech

Cleaning Validation Engineer

Minneapolis, MN

$90K - $105K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Your Role The Cleaning Validation Engineer is responsible for the development, modification, execution, and reporting of cleaning validation activities supporting biopharmaceutical manufacturing ...

PSC Biotech

Cleaning Validation Engineer

Minneapolis, MN

$90K - $105K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Your Role The Cleaning Validation Engineer is responsible for the development, modification, execution, and reporting of cleaning validation activities supporting biopharmaceutical manufacturing ...

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Cleaning Validation information

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How much do cleaning validation jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for cleaning validation in the United States is $39.42, according to ZipRecruiter salary data. Most workers in this role earn between $37.98 and $40.87 per hour, depending on experience, location, and employer.

What is the job description of cleaning validation?

Cleaning validation is a process used in pharmaceutical and manufacturing industries to ensure that cleaning procedures effectively remove contaminants from equipment and surfaces. The job involves developing, executing, and documenting validation protocols, performing residue testing, and ensuring compliance with regulatory standards. Skills in analytical testing, attention to detail, and knowledge of Good Manufacturing Practices (GMP) are essential for this role.

What is the difference between Cleaning Validation vs Microbiologist?

AspectCleaning ValidationMicrobiologist
Required credentialsGMP, GMP-related certifications, technical trainingBiology, microbiology degrees, certifications
Work environmentPharmaceutical, biotech manufacturing facilitiesLaboratories, research facilities, healthcare settings
Employer and industry usagePharmaceutical, biotech, food industriesHealthcare, research, environmental testing

Cleaning Validation focuses on ensuring that cleaning processes effectively remove contaminants from equipment, primarily in manufacturing settings. Microbiologists study microorganisms, their behaviors, and control methods, often working in labs. While both roles require scientific knowledge and certifications, Cleaning Validation specialists concentrate on process validation in production environments, whereas Microbiologists focus on microbial analysis and research.

How do you become a cleaning validation consultant?

To become a cleaning validation consultant, professionals typically need a background in pharmaceutical or biotech manufacturing, quality assurance, or related fields, along with knowledge of validation processes and regulatory requirements such as FDA or EMA guidelines. Gaining experience through roles in validation, quality control, or manufacturing, and obtaining certifications like ASQ Certified Quality Auditor or specific validation training, can enhance credibility. Strong analytical skills, attention to detail, and familiarity with cleaning procedures and documentation are essential for success in this role.

What does cleaning validation do?

Cleaning validation is a process used in quality assurance roles to ensure that cleaning procedures effectively remove contaminants from equipment, preventing cross-contamination and ensuring product safety. It involves testing and documenting cleaning processes, often requiring knowledge of regulatory standards and analytical methods. Proper cleaning validation helps maintain compliance and product quality in regulated industries.
More about Cleaning Validation jobs
What cities are hiring for Cleaning Validation jobs? Cities with the most Cleaning Validation job openings:
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Cleaning Validation jobs near you
Infographic showing various Cleaning Validation job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 66% Full Time, 30% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 100% Physical job distribution, with an average salary of $82,000 per year, or $39.4 per hour.

Cleaning Validation Specialist

Moriah Engineering

PR • On-site

Contractor

Re-posted 27 days ago

Job description

Salary:

Job Summary:


The Cleaning Validation Specialist will be responsible for developing, executing, and managing cleaning validation activities to ensure compliance with regulatory requirements and internal quality standards. The role focuses on ensuring the effectiveness and consistency of cleaning processes, particularly for manufacturing equipment and related systems, including utilities and compressed air systems. The ideal candidate will bring expertise in cleaning validation, utilities qualification, and a strong understanding of GMP regulations.


Responsibilities:

Develop and implement cleaning validation protocols and reports, ensuring compliance with GMP, FDA, and other regulatory standards.
Plan and execute cleaning validation activities for manufacturing equipment and utilities, including compressed air systems.
Conduct risk assessments and identify critical control points for cleaning validation.
Perform sampling and testing of cleaned equipment and utilities to ensure compliance with predetermined acceptance criteria.
Collaborate with cross-functional teams, including Quality Assurance, Manufacturing, and Engineering, to define cleaning validation requirements and processes.
Develop and implement protocols for utilities qualification and monitoring, with a focus on compressed air systems.
Analyze data to identify trends and recommend process improvements to enhance cleaning and utilities validation performance.
Manage deviations and non-conformances related to cleaning validation activities, ensuring timely investigation and resolution.
Maintain detailed and accurate documentation of cleaning validation and utilities qualification activities.
Ensure the consistent implementation of cleaning validation processes across manufacturing operations.
Support audits and inspections by regulatory authorities, providing expertise in cleaning validation and utilities processes.
Stay current with industry trends and regulatory updates, ensuring continuous compliance and the adoption of best practices.

Qualifications:


Bachelors Degree in Engineering, Chemistry, Microbiology, or a related field.
2+ years of experience in cleaning validation within a regulated manufacturing environment.
Experience in utilities qualification, particularly compressed air systems.
Strong knowledge of regulatory requirements, including GMP, FDA, and ICH guidelines.
Proficiency in developing and executing cleaning validation protocols and reports.
Demonstrated experience in risk assessment and data analysis for cleaning validation.
Excellent problem-solving and analytical skills.
Strong communication and interpersonal skills to collaborate with cross-functional teams and external auditors.
Proficiency in software tools such as MS Excel, Word, PowerPoint, and project management tools.
Physical/Mental Requirements:

Ability to work in a manufacturing environment, including cleanrooms and production areas.
Able to stand for extended periods and climb ladders/steps as needed.
Ability to lift and move items up to 25 lbs.


About the Company:
We consider all applicants for all positions regardless of race, color, religion, gender, sexual orientation, gender identity, national origin, age, protected veteran status, or any other characteristic protected by law. We value diversity and promote an inclusive environment where all employees can thrive.