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Contract Cleaning Validation Engineer Jobs (NOW HIRING)

Validation & Engineering Group, Inc

PR · On-site

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 · On-site

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 · On-site

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 · On-site

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 · On-site

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 · On-site

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 · On-site

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 · On-site

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 · On-site

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 ...

Sebela Pharma

CQV/Validation Engineer

Holbrook, MA · On-site

$33 - $43/hr

Braintree Laboratories, Inc., a part of Sebela Pharmaceuticals, has its contract development and ... Support equipment, utility, facility, process, cleaning, and computerized system validation ...

INCOG

Senior Validation Engineer

Fishers, IN · On-site

The Senior Validation Engineer is responsible for understanding and implementing validation ... This includes, but is not limited to, clean utilities, autoclave, washer, filler, laboratory ...

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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 Jul 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.
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What cities are hiring for Contract Cleaning Validation Engineer jobs? Cities with the most Contract Cleaning Validation Engineer job openings:
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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 July 2026, with employment types broken down into 61% Full Time, 38% Part Time, and 1% Temporary. Highlights an 100% Physical job distribution, with an average salary of $108,152 per year, or $52 per hour.

Cleaning Validation Specialist

Technical and Engineering Consulting

Carolina, PR

Other

Re-posted 25 days ago

Job description

Position Overview

We are seeking a Cleaning Validation Specialist to support critical manufacturing operations at the solid dosage manufacturing site. This role will play a key part in cleaning validation program execution and digital transformation initiatives, including the implementation of enhanced data integrity practices and migration of cleaning documentation into a new digital platform.

The ideal candidate will bring strong technical expertise in cleaning validation, combined with the ability to collaborate across multidisciplinary teams to improve processes, ensure compliance, and drive operational excellence.

Key Responsibilities

  • Actively participate in Cleaning Validation team meetings, providing updates on timelines, risks, and project status.

  • Evaluate and understand manufacturing equipment cleaning processes and identify opportunities for improvement.

  • Develop and execute cleaning validation protocols, reports, and executable instructions.

  • Support digital transformation efforts by transferring paper-based cleaning documentation into a new digital platform.

  • Assess and enhance data integrity controls within cleaning validation processes and documentation.

  • Serve as Subject Matter Expert (SME) for cleaning validation activities and compliance requirements.

  • Review and approve key documentation, including:

    • Cleaning Validation Master Plans

    • Risk Assessments

    • Protocols and Reports

    • SOPs and Work Instructions

  • Lead and/or support change control activities, including:

    • Impact assessments

    • Change control generation

    • Presentation to Change Control Board

  • Participate in triage and risk assessment activities related to process or documentation changes.

  • Review and optimize equipment cleaning instructions during digital platform migration.

  • Support data integrity assessments and remediation actions for the cleaning program.

  • Provide training to manufacturing personnel on cleaning processes and compliance requirements.

  • Support on-call rotation for cleaning execution activities as required.

  • Ensure compliance with training systems (e.g., Darwin, TrackWise, Veeva Quality Docs).

  • Perform additional duties as assigned by leadership.

Qualifications

  • Bachelor's Degree in Engineering, Chemistry, Microbiology, or related Science field.

  • 3-7+ years of experience in cleaning validation within pharmaceutical or regulated manufacturing environments.

  • Strong knowledge of:

    • cGMP / FDA regulations

    • Cleaning validation lifecycle and strategies

    • Data integrity principles (ALCOA+)

  • Experience with:

    • Protocol and report generation (IQ/OQ/PQ / CV)

    • Risk assessments and limit calculations

    • Change control systems (e.g., TrackWise)

    • Document management systems (e.g., Veeva)

  • Experience supporting digital platforms or paperless validation systems is highly preferred.

  • Strong technical writing, analytical, and problem-solving skills.

  • Fully bilingual (English / Spanish) with excellent communication skills.

  • Ability to work independently with limited supervision and in cross-functional teams.

Preferred Qualifications

  • Experience in oral solid dosage (OSD) or similar manufacturing environments.

  • Exposure to data integrity remediation projects.

  • Previous experience leading training sessions or acting as SME.

Why Join This Opportunity?

  • Be part of a high-impact digital transformation initiative within a leading pharmaceutical environment.

  • Work alongside a multidisciplinary team driving compliance and innovation.

  • Opportunity to contribute to process improvements and regulatory excellence.

Apply