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Contract Cleaning Validation Engineer Jobs (NOW HIRING)

Quality Agents

Validation Engineer II

Rockville, MD · On-site

... cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the Validation Engineer must be approved by the client.

Quality Agents

Validation Engineer IV

Rockville, MD · On-site

... cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the Validation Engineer must be approved by the client.

Stryker Corporation

$85 - $125/hr

The ideal candidate will have hands-on experience in equipment, process, cleaning, and computerized ... Engineering, and Regulatory teams to ensure compliance with validation requirements. * Ensure ...

New

Stark Pharma Solutions Inc

IL · On-site

Manufacturing Validation Engineer Location: Lake County, IL Duration: Long Term Position Overview ... Familiarity with computerized systems validation (CSV), cleaning validation, or utility ...

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How much do contract cleaning validation engineer jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for contract cleaning validation engineer in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

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.

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Contract Cleaning Validation Engineer jobs near you
Infographic showing various Contract Cleaning Validation Engineer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 64% Full Time, 32% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Engineer, Cleaning Validation Specialist

3 Key Consulting

Holly Springs, NC • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Engineer, Cleaning Validation Specialist3 Key Consulting is hiring an Engineer, Cleaning Validation Specialist for a consulting engagement with our direct client, a leading global biopharmaceutical company.Job Description:Our ideal candidate: 5+ YOE with a B.S. in Science, Engineering, and Pharmacy areas.This is a Cleaning Validation Specialist position. Candidate will coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning development and validation. Perform investigation of deviations / discrepancies.Support authoring and executing CV/CHT/SHT protocols, progress package work and wrap up executed studiesSupports non-traditional work schedule based on project and business needsFamiliar with Drug substance process equipment, autoclaves, parts washers, CIP skids to support CV programDemonstrated proficiency in utilizing PI for run trending analysis and facilitating the successful completion of support packages.Leads and performs on floor CV execution and sampling. Provide technical support and sample management to cleaning activities associated with the manufacturing process.Proficient with KNEAT executionDesign and develop cleaning procedures for new products and manufacturing equipment.Investigates and conducts troubleshooting/root cause analysis of cleaning related incidents, deviations and cleaning out of specification results for non-validated or under development cleaning procedures.Supports the periodic review of cleaning validation studies.Performs successful and on time resolution of incidents and deviations related to cleaning validation exercises.Collaborate with cross-functional teams, including Quality Assurance, Manufacturing, and Engineering, to ensure cleaning validation activities are integrated into the overall project plan.Trains manufacturing and QC/QA personnel on cleaning validation documentation.Why is the Position Open?Planned ProjectTop Must Have Skills:Proficient with KNEAT or similar programs.Strong understanding of GMPs and global regulatory expectations.Ability to interpret equipment design, P&IDs, and process flow diagrams.Excellent technical writing and documentation skills.Strong analytical and problem solving abilities.Effective communication and cross-functional collaboration.Ability to work independently and manage multiple priorities.Day to Day Responsibilities:Expectation is that the candidate will support execution and management of the CV lifecycle.Support authoring and executing CV/CHT/SHT protocols, progress package work and wrap up executed studiesSupports non-traditional work schedule based on project and business needsFamiliar with Drug substance process equipment, autoclaves, parts washers, CIP skids to support CV programDemonstrated proficiency in utilizing PI for run trending analysis and facilitating the successful completion of support packages.Leads and performs on floor CV execution and sampling. Provide technical support and sample management to cleaning activities associated with the manufacturing process.Proficient with KNEAT executionDesign and develop cleaning procedures for new products and manufacturing equipment.Investigates and conducts troubleshooting/root cause analysis of cleaning related incidents, deviations and cleaning out of specification results for non-validated or under development cleaning procedures.Supports the periodic review of cleaning validation studies.Performs successful and on time resolution of incidents and deviations related to cleaning validation exercises.Collaborate with cross-functional teams, including Quality Assurance, Manufacturing, and Engineering, to ensure cleaning validation activities are integrated into the overall project plan.Trains manufacturing and QC/QA personnel on cleaning validation documentation.Basic Qualifications:Master degree or Bachelor degree and 2 years of experience or Associate degree and 6 years of experience or high school diploma / GED and 8 years of experiencePreferred Qualifications:Project Management experience.Red Flags:Lack of experience on the floor or supporting field execution Inability to support non-traditional work scheduleInterview process:First round virtual screening 2nd round panel onsite.

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