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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 ... Cleaning Validation Specialist We are looking for a resource to support the development and ...

Gilead

Cleaning Validation Engineer II

La Verne, CA

$99K - $129K/yr

Lead and execute cleaning validation activities for a multiproduct facility , including parenteral ... Collaborate with cross-functional teams (Manufacturing, Quality, Engineering, etc.) to support ...

Validation & Engineering Group, Inc

PR · On-site

Experience supporting various manufacturing equipment and/or systems, as well as Cleaning Validation. * Among other related activities. At Validation & Engineering Group, people always come first. We ...

Intellectt INC

Validation Engineer II

Bothell, WA · On-site

My name is Vyshu, and I'm reaching out from Intellectt Inc. regarding an exciting contract ... Cleaning validation experience * Exposure to PPQ * Utilities/facility qualification experience

BioPhase Solutions

Validation Engineer

Los Angeles, CA · On-site

$115K/yr

... contract development and manufacturing organization. Salary: $100-115k+/year depending on ... Execute Process Validation and Cleaning Validation: Identify critical process parameters, establish ...

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 ...

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Contract Cleaning Validation Engineer information

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$51

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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.
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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 Engineer

Eliquent Life Sciences, Inc

Montrose, CA • On-site

Full-time

Posted 19 days ago

Job description

About Company:

Who Are We?

ELIQUENT Life Sciences is a leading global consulting group delivering regulatory affairs, pharmacovigilance, quality, and compliance solutions that support pharmaceutical, biotechnology, medical device, and combination product companies across therapeutic modalities, phase-based pathways, and major global markets.


Why explore your future at ELIQUENT?

ELIQUENT Life Sciences is a trusted global consulting firm helping life sciences companies navigate regulatory complexity and bring breakthrough therapies to market. Founded by former regulators and industry experts, we offer end-to-end support in regulatory affairs, pharmacovigilance, and quality compliance. Our team is driven by a shared mission to improve global health through innovation, collaboration, and integrity. At ELIQUENT, you will be part of a purpose-led organization where your expertise contributes to meaningful impact and your growth is supported every step of the way.


About the Role:

The Cleaning Validation Engineer plays a critical role in ensuring that pharmaceutical manufacturing equipment and processes meet stringent cleanliness standards to guarantee product safety and regulatory compliance. This position is responsible for designing, executing, and maintaining cleaning validation protocols that confirm the effective removal of contaminants and residues from manufacturing systems. The engineer collaborates closely with cross-functional teams including quality assurance, production, and engineering to develop scientifically sound validation strategies aligned with industry best practices and regulatory requirements. By analyzing data and continuously improving cleaning processes, the role helps to minimize risks of cross-contamination and supports the overall integrity of pharmaceutical products. Ultimately, the Cleaning Validation Engineer ensures that all cleaning activities are validated, documented, and compliant with FDA, EMA, and other relevant regulatory bodies, thereby safeguarding patient health and company reputation.

Minimum Qualifications:

  • Bachelor’s degree in Pharmaceutical Engineering, Chemical Engineering, or a related scientific discipline.
  • Demonstrated experience in cleaning validation within pharmaceutical manufacturing environments.
  • Strong knowledge of Sterilize-In-Place (SIP) systems and pharmaceutical manufacturing processes.
  • Familiarity with regulatory requirements such as FDA, EMA, and ICH guidelines related to cleaning validation.
  • Proficiency in developing and executing validation protocols and technical reports.

Preferred Qualifications:

  • Advanced degree (Master’s or higher) in Pharmaceutical Engineering or related field.
  • Experience with automation and control systems used in pharmaceutical manufacturing.
  • Certification in validation or quality assurance (e.g., ASQ Certified Quality Engineer).
  • Hands-on experience with analytical techniques such as HPLC, TOC, or ATP bioluminescence for cleaning verification.
  • Strong project management skills and experience leading cross-functional validation projects.

Responsibilities:

  • Develop, review, and execute cleaning validation protocols and reports in accordance with cGMP and regulatory guidelines.
  • Perform risk assessments and establish acceptance criteria for cleaning processes based on product and equipment characteristics.
  • Collaborate with manufacturing and quality teams to identify critical cleaning parameters and optimize cleaning procedures.
  • Conduct sampling, analytical testing, and data analysis to verify the effectiveness of cleaning processes.
  • Maintain comprehensive documentation and ensure all validation activities are audit-ready and compliant with regulatory standards.
  • Investigate and resolve deviations or non-conformances related to cleaning validation activities.
  • Stay current with industry trends, regulatory changes, and emerging technologies to continuously improve cleaning validation practices.

Skills:

The required skills such as expertise in SIP systems and pharmaceutical manufacturing processes are applied daily to design and optimize cleaning validation protocols that ensure equipment cleanliness and product safety. Pharmaceutical engineering knowledge enables the engineer to understand complex manufacturing systems and develop scientifically robust validation strategies. Analytical skills are essential for interpreting test results and making data-driven decisions to improve cleaning procedures. Preferred skills like familiarity with advanced analytical techniques and automation systems enhance the engineer’s ability to implement innovative solutions and increase validation efficiency. Effective communication and project management skills facilitate collaboration with multidisciplinary teams and ensure timely completion of validation projects in compliance with regulatory standards.