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Contract Cleaning Validation Engineer Jobs (NOW HIRING)

Intellectt INC

Validation Engineer

San Diego, CA · On-site

Validation Engineer Location: San Diego, CA Duration: Longterm Job Summary: A Validation Engineer ... Execute validation protocols for equipment qualification, process validation, cleaning validation ...

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 ...

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 ...

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 ...

Catalent, Inc.

Validation Engineer

Chelsea, MA · On-site

$89K - $110K/yr

The Validation Engineer is responsible for executing validation activities within a GMP ... Provide technical support to key site programs, including the cleaning program (cleaning validation ...

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 ...

Catalent Pharma Solutions

Validation Engineer

Chelsea, MA · On-site

$89K - $110K/yr

The Validation Engineer is responsible for executing validation activities within a GMP ... Provide technical support to key site programs, including the cleaning program (cleaning validation ...

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 ...

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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 13, 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 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.
Validation Engineer II

Validation Engineer II

Quality Agents, LLC

Rockville, MD • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago

Job description

Quality Agents, LLC is a service company offering validation and quality expertise to the pharmaceutical and biotechnology industries. Our Validation Engineers will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The Validation Engineer will evaluate the equipment/utility/system/procedures used in development, production, and holding of pharmaceutical products and determine a validation approach. The individual should have experience with current US and international regulations, guidance, industry best practice in one of the following areas of validation: facilities, utilities, and equipment qualifications, process validation, analytical method validation, or 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.
Responsibilities include:
  • Interact with clients and works closely with site manufacturing, engineering, and QA to develop validation documents.
  • Travel to various client sites and work independently to complete tasks.
  • Provide qualification and validation services for cGMP manufacturing equipment, systems, and utilities at client sites.
  • Exposure to validation aspects of facility start-up, redesign/retrofit, and expansion.
  • Writes and executes qualification protocols for a variety of biopharmaceutical equipment and support utilities in accordance with SOPs, master plans, regulatory expectations, and industry standards.
  • Conducts temperature mapping studies, including the operation of Kaye dataloggers, or equivalent.
  • Review and approve documented test results and maintain records for later analysis.
  • Assist with non-conformances, investigations, and troubleshooting of equipment, utilities, and systems.
  • Able to read P&IDs, isometric drawings, and As-built drawings.

Skill Level and Requirements:
  • Ability to problem solve and troubleshoot.
  • Technical writing ability and use of Microsoft Word, Excel, Power point, and Project
  • Experience with validation equipment such as the Kaye validator, wireless data loggers, or other monitoring devices is strongly desired.
  • Experience using statistical tools is a plus to analyze data captured during validation studies.

Minimum Requirements:
  • BS in a technical discipline (Engineering, chemistry, microbiology, biology)
  • 2 - 5 years of experience in at least one of the following areas: equipment/utility qualifications, process validation, analytical method validation, or cleaning validation.
  • Current driver's license and auto insurance

Quality Agents offers a full suite of benefits for full-time employees including:
  • Health, dental and vision insurance
  • Life, AD&D and disability Insurance
  • Health savings account for participants in our health plan
  • 401k retirement plan
  • Paid time off
  • Paid holidays

Quality Agents accepts applications on an on-going basis in order to build a talent pool of potential candidates. These applications remain open for consideration, as positions become available, for one (1) year from the date of application. After that time, or if your application information changes, please submit your application again.

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