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Cleaning Validation Jobs (NOW HIRING)

Intellectt INC

"cleaning validation"

Holly Springs, NC · On-site

Role:CQV Engineer - Cleaning Validation Location: Holly Springs, NC Key Responsibilities: * Execute and document cleaning validation protocols per FDA/ICH guidelines (ALCOA principles). * Apply ...

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 ...

Cencora

Cleaning Validation Specialist

Juncos, PR

Coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning development and validation. Perform investigation of deviations / discrepancies. Responsibilities:

Cencora

Cleaning Validation Specialist

Carolina, PR

Coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning development and validation. Perform investigation of deviations / discrepancies. Responsibilities:

Cencora

Cleaning Validation Specialist

Juncos, PR · On-site

Coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning development and validation. Perform investigation of deviations / discrepancies. Responsibilities:

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Cleaning Validation information

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$36

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$42

How much do cleaning validation jobs pay per hour?

As of Jun 24, 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.

How to become a cleaning validation consultant?

To become a cleaning validation consultant, professionals typically need a background in pharmaceutical or biotech manufacturing, with knowledge of validation processes and regulatory standards such as FDA or EMA guidelines. Gaining experience in cleaning procedures, validation protocols, and quality assurance is essential, often complemented by certifications like ASQ or ISPE training. Strong analytical skills and familiarity with validation tools and documentation are also important for success in 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 to become a validation specialist?

To become a validation specialist, typically one needs a background in life sciences, engineering, or a related field, along with experience in quality assurance or manufacturing. Certification in validation processes, such as those from ISPE or PDA, can enhance prospects, and familiarity with regulatory standards like GMP is essential. Strong attention to detail and knowledge of validation tools and documentation are also important.

Do validation engineers make good money?

Validation engineers, including those in cleaning validation, typically earn competitive salaries that vary by industry, experience, and location. They often require knowledge of regulatory standards and validation processes, which can lead to higher compensation as they gain expertise. Overall, validation engineering is considered a well-paying field within quality assurance roles.

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 manufacturing environments.
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Cleaning Validation jobs near you
"cleaning validation"

"cleaning validation"

Intellectt INC

Holly Springs, NC • On-site

Contractor

Posted 11 days ago

Job description

Role:CQV Engineer – Cleaning Validation 
Location: Holly Springs, NC 
Key Responsibilities:

  • Execute and document cleaning validation protocols per FDA/ICH guidelines (ALCOA principles).

  • Apply expertise with bioreactors, autoclaves, parts washers, and filling machines.

  • Perform MACO calculations to support cleaning limit determinations.

  • Use Kneat for electronic validation documentation and tracking.

  • Work on fill-finish processes and equipment validation.

  • Coordinate with cross-functional teams including manufacturing, QC, QA, and engineering.

  • Review and contribute to analytical method development related to cleaning and residue testing.

Required Skills & Experience:

  • 5–8+ years in CQV/Validation within biologics/pharmaceutical manufacturing.

  • Strong understanding of FDA cGMP, ALCOA, and data integrity principles.

  • Experience with Kneat or other electronic validation tools.

  • Familiarity with MACO, analytical methods, and technical documentation.

  • Must have experience with fill-finish processes, bioreactors, and cleaning equipment.