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Contract Cleaning Validation Engineer Jobs (NOW HIRING)

Valspec

Validation Engineer - Kentucky

Lexington, KY · On-site

Validation Engineer Job Type: [Full-time/Contract] Valspec is seeking a highly motivated and detail-oriented Cleaning Validation Engineer to join our dynamic team. The successful candidate will play ...

Gilead

Cleaning Validation Engineer II

La Verne, CA · On-site

$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 ...

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 ...

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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 Jun 9, 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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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 May 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.
Cleaning Validation Engineer

Cleaning Validation Engineer

Sterling Engineering Inc.

Crystal Lake, IL • On-site

$95K - $105K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 18 days ago

Job description

Job Title: Cleaning Validation Engineer
Location: Crystal Lake
Hire Type: Direct Hire
Compensation: $95,000–$105,000/year
Benefits: PTO, paid holidays, medical/dental/vision, retirement plan
Position Summary:
We are seeking a Cleaning Validation Engineer to support cleaning validation activities within a GMP-regulated pharmaceutical manufacturing environment. This role is responsible for developing, executing, and maintaining cleaning validation programs to ensure manufacturing equipment and processes meet regulatory and quality standards.
The ideal candidate will have experience with cleaning validation protocols, technical documentation, GMP compliance, and cross-functional collaboration within pharmaceutical manufacturing.
Key Responsibilities:
  • Lead cleaning validation activities for new equipment, process changes, and continuous improvement projects
  • Develop and execute cleaning validation protocols, sampling plans, and final reports
  • Evaluate validation data to ensure cleaning effectiveness, repeatability, and compliance
  • Support change controls, deviations, investigations, and CAPAs related to cleaning validation
  • Partner with Manufacturing, Engineering, QA, QC, and Regulatory teams on validation initiatives
  • Assist with residue limits, recovery studies, and acceptance criteria development
  • Maintain validation documentation, SOPs, and quality standards
  • Support internal and external regulatory inspections as a cleaning validation SME
  • Review and approve controlled documents within area of expertise
  • Support training and mentoring of validation personnel as needed
Qualifications:
  • Bachelor’s degree in Engineering, Chemistry, Biology, or related scientific discipline preferred
  • 3+ years of validation experience in pharmaceutical manufacturing
  • Direct cleaning validation experience strongly preferred
  • Strong understanding of cGMPs, validation principles, and regulated manufacturing environments
  • Experience writing and executing validation protocols and reports
  • Excellent technical writing, analytical, and problem-solving skills
  • Ability to manage multiple priorities in a fast-paced environment
  • Strong communication and cross-functional collaboration skills


Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.