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Cleaning Validation Engineer Jobs (NOW HIRING)

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 ...

Valspec

Validation Engineer - Kentucky

Lexington, KY · On-site

Validation Engineer Job Type: [Full-time/Contract] Valspec is seeking a highly motivated and detail ... Develop, execute, and oversee cleaning validation strategies and protocols for solid dose ...

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

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

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

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How much do cleaning validation engineer jobs pay per hour?

As of Jun 7, 2026, the average hourly pay for 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 are the key skills and qualifications needed to thrive in the Cleaning Validation Engineer position, and why are they important?

To thrive as a Cleaning Validation Engineer, you need a strong background in chemical engineering, microbiology, or a related field, often complemented by experience in GMP-regulated industries. Familiarity with validation protocols, analytical testing methods, and documentation tools (such as LIMS or QMS software) is essential, and certifications like Six Sigma or ASQ may be advantageous. Strong attention to detail, analytical thinking, and effective communication are key soft skills for success in the role. These capabilities are crucial to ensure regulatory compliance, product safety, and effective cross-functional collaboration in pharmaceutical or biotech manufacturing environments.

What is a Cleaning Validation Engineer job?

A Cleaning Validation Engineer ensures that manufacturing equipment and processes meet regulatory standards for cleanliness in industries like pharmaceuticals, biotech, and medical devices. They develop validation protocols, conduct tests, analyze data, and document results to confirm that cleaning procedures effectively remove contaminants. This role involves collaborating with quality assurance, production, and regulatory teams to maintain compliance with FDA, GMP, and other industry regulations.

What are the main challenges faced by Cleaning Validation Engineers in the pharmaceutical industry?

Cleaning Validation Engineers in the pharmaceutical industry often face challenges such as staying up-to-date with evolving regulatory requirements, troubleshooting complex cleaning failures, and thoroughly documenting all validation activities. Balancing the needs for robust contamination control with operational efficiency requires analytical thinking and strong problem-solving abilities. Collaboration with manufacturing, quality assurance, and laboratory teams is frequent, as cleaning validation projects require input and support from multiple departments. Successfully managing these challenges ensures product safety, regulatory compliance, and continuous process improvement within manufacturing operations.

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What cities are hiring for Cleaning Validation Engineer jobs? Cities with the most Cleaning Validation Engineer job openings:
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Cleaning Validation Engineer jobs near you
Infographic showing various Cleaning Validation Engineer job openings in the United States as of May 2026, with employment types broken down into 96% Full Time, 1% Part Time, and 3% Contract. Highlights an 99% Physical, and 1% Remote 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

$95K - $105K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 16 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.