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Contract Cleaning Validation Engineer Jobs (NOW HIRING)

kindeva

Validation Engineer II

Saint Louis, MO · On-site

This role assists with equipment qualification, aseptic process validation, cleaning validation ... Bachelor's degree in Engineering, Chemistry, Biochemistry, Microbiology, Pharmacy or related ...

kindeva

Validation Engineer II

Saint Louis, MO · On-site

This role assists with equipment qualification, aseptic process validation, cleaning validation ... Bachelor's degree in Engineering, Chemistry, Biochemistry, Microbiology, Pharmacy or related ...

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

Collaborate with cross-functional teams, including Quality Assurance, Manufacturing, and Engineering, to define cleaning validation requirements and processes. Develop and implement protocols for ...

Validation & Engineering Group, Inc

PR

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... This role ensures that cleaning and sterilization systems are installed, tested, and qualified in ...

Validation & Engineering Group, Inc

PR

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... This role ensures that cleaning and sterilization systems are installed, tested, and qualified in ...

Validation & Engineering Group, Inc

PR

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... This role ensures that cleaning and sterilization systems are installed, tested, and qualified in ...

Validation & Engineering Group, Inc

PR

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... This role ensures that cleaning and sterilization systems are installed, tested, and qualified in ...

Validation & Engineering Group, Inc

PR

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... This role ensures that cleaning and sterilization systems are installed, tested, and qualified in ...

Validation & Engineering Group, Inc

PR

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... This role ensures that cleaning and sterilization systems are installed, tested, and qualified in ...

Validation & Engineering Group, Inc

PR

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... This role ensures that cleaning and sterilization systems are installed, tested, and qualified in ...

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All JobsContract Cleaning Validation Engineer Jobs

Contract Cleaning Validation Engineer information

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$22

$51

$78

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

As of Jun 14, 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 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 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 are Contract Cleaning Validation Engineers?

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, and why are they important?

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.
More about Contract Cleaning Validation Engineer jobs
What cities are hiring for Contract Cleaning Validation Engineer jobs? Cities with the most Contract Cleaning Validation Engineer job openings:
What are the most commonly searched types of Cleaning Validation Engineer jobs? The most popular types of Cleaning Validation Engineer jobs are:
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What job categories do people searching Contract Cleaning Validation Engineer jobs look for? The top searched job categories for Contract Cleaning Validation Engineer jobs are:
Contract Cleaning Validation Engineer jobs near you
Infographic showing various Contract Cleaning Validation Engineer job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $108,152 per year, or $52 per hour.

Validation Engineer II

kindeva

Saint Louis, MO • On-site

Other

Posted 10 days ago

Kindeva rating

6.8

Company rating: 6.8 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

Job description

Our Work Matters

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

The Impact You Will Make

The Floater Validation Engineer II provides validation engineering support across two pharmaceutical aseptic manufacturing facilities and one inspection and packaging site. This role assists with equipment qualification, aseptic process validation, cleaning validation, computer systems validation, and inspection/packaging validation activities. The position delivers flexible, cross-site validation coverage while executing protocols, performing testing, and authoring validation documentation under the direction of the Validation Manager.

Responsibilities

• Provide validation support across multiple sites based on business priorities.

• Assist in equipment qualification (IQ/OQ/PQ), cleaning validation, process validation, and CSV.

• Execute and author validation protocols and reports.

• Support aseptic manufacturing and inspection/packaging validation activities.

• Issue validation data, protocols, reports, and technical memos.

• Support site change management programs and maintain validated states.

• Assist with Validation Master Plans and Continuous Process Verification activities.

• Review vendor turnover packages and User Requirement Specifications.

Qualifications

  • Bachelor’s degree in Engineering, Chemistry, Biochemistry, Microbiology, Pharmacy or related discipline
  • 5+ years of relevant validation or pharmaceutical manufacturing experience, or equivalent combination of education and experience.
  • Knowledge of cGMP and regulatory guidance.
  • Experience in aseptic manufacturing and inspection/packaging operations.
  • Ability to interpret technical documentation and identify deviations.

• Proficiency with Microsoft Office applications.

  • Regular travel between sites required; ability to adapt to multiple GMP environments.

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