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Cleaning Validation Jobs (NOW HIRING)

3B Staffing LLC

Validation Engineer

Mount Prospect, IL · On-site

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

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Cleaning Validation information

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How much do cleaning validation jobs pay per hour?

As of Sep 4, 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 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.

What are the guidelines for cleaning validation?

Cleaning validation for a Cleaning Validation specialist involves establishing written procedures, verifying that cleaning processes effectively remove residues, and documenting validation activities. It typically includes setting acceptance criteria, performing residue testing, and conducting repeated validations to ensure consistent cleaning performance, often using analytical methods like HPLC. Compliance with regulatory standards such as GMP is essential, and validation protocols should be reviewed and approved before implementation.

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.
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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, 31% Part Time, 1% Temporary, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $82,000 per year, or $39.4 per hour.

CQV / CLEANING VALIDATION ENGINEER

Weil Group, Inc.

Juncos, PR • On-site

Full-time

Posted 4 days ago

Job description

Position Summary
The CQV/Cleaning Validation Engineer will develop and execute Cleaning Characterization and Cleaning Verification documentation and field activities for manufacturing equipment and process systems.
Key Responsibilities
•Prepare Cleaning Characterization protocols and final reports.
•Review applicable manufacturing procedures, batch records, equipment drawings, P&IDs, isometrics, and process recipes.
•Review equipment sequence of operations and cleaning cycles.
•Evaluate CIP/SIP circuits as applicable.
•Perform product contact surface area calculations.
•Perform field verification of equipment dimensions and product contact surfaces when information is not available or needs to be confirmed.
•Prepare sampling plans for TOC and microbiological surface sampling.
•Perform or support swab sampling and other sample collection activities required by the protocol.
•Coordinate sample labeling, custody, and delivery to the QC laboratory.
•Participate in Engineering Runs, Pre-PPQ, PPQ, changeover, and Release for Use activities, as required.
•Review process data and results against established acceptance criteria.
•Generate and review PI Historian trends, as applicable.
•Document discrepancies and support related investigation activities.
•Prepare final reports within the established project timelines.
•Perform peer review of calculations, data, and execution results when required.
•Provide execution support during off-shifts, weekends, or extended hours based on project needs.
Minimum Recommended Qualifications
•Bachelor's degree in Engineering, Chemistry, Microbiology, Biotechnology, Life Sciences, or related discipline.
•Minimum 5 years of pharmaceutical/biotechnology CQV or validation experience.
•Minimum 3 years of Cleaning Validation or Cleaning Verification experience.
•Knowledge of CIP systems, cleaning cycles, sampling strategies, TOC, and microbiological testing.
*Weil Group is proud to be an Equal Employment Opportunity Employer.*

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