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Assistant Cleaning Validation Engineer Jobs (NOW HIRING)

Gilead

Cleaning Validation Engineer II

La Verne, CA · On-site

$99.71K - $129.03K/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 ...

3B Staffing LLC

Validation Engineer

Mount Prospect, IL · On-site

Validation Engineer Coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning development and validation. Perform investigation of deviations / discrepancies.

kindeva

Validation Engineer II

Saint Louis, MO · On-site

... priorities. • Assist in equipment qualification (IQ/OQ/PQ), cleaning validation, process ... Bachelor's degree in Engineering, Chemistry, Biochemistry, Microbiology, Pharmacy or related ...

kindeva

Validation Engineer II

Saint Louis, MO · On-site

... priorities. • Assist in equipment qualification (IQ/OQ/PQ), cleaning validation, process ... Bachelor's degree in Engineering, Chemistry, Biochemistry, Microbiology, Pharmacy or related ...

kindeva

Validation Engineer II

Saint Louis, MO · On-site

... priorities. • Assist in equipment qualification (IQ/OQ/PQ), cleaning validation, process ... Bachelor's degree in Engineering, Chemistry, Biochemistry, Microbiology, Pharmacy or related ...

kindeva

Validation Engineer II

Saint Louis, MO

... priorities. • Assist in equipment qualification (IQ/OQ/PQ), cleaning validation, process ... Bachelor's degree in Engineering, Chemistry, Biochemistry, Microbiology, Pharmacy or related ...

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Assistant Cleaning Validation Engineer information

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$33K

$88.8K

$134.5K

How much do assistant cleaning validation engineer jobs pay per year?

As of May 28, 2026, the average yearly pay for assistant cleaning validation engineer in the United States is $88,754.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,500.00 and $104,500.00 per year, depending on experience, location, and employer.

What is the difference between Assistant Cleaning Validation Engineer vs Cleaning Validation Engineer?

AspectAssistant Cleaning Validation EngineerCleaning Validation Engineer
CredentialsTypically requires a bachelor's degree in life sciences or engineering; certifications like ASQ or GMP training are commonRequires similar qualifications; often more experience or advanced certifications
Work EnvironmentSupports validation activities in pharmaceutical or biotech manufacturing facilitiesLeads validation projects, performs complex testing, and reviews validation protocols
Employer & IndustryPharmaceutical, biotech, or medical device companiesSame industries, with more senior responsibilities

The Assistant Cleaning Validation Engineer typically supports validation tasks under supervision, focusing on executing protocols and data collection. In contrast, the Cleaning Validation Engineer oversees validation processes, reviews results, and ensures compliance. Both roles are essential in maintaining product quality and regulatory standards in pharmaceutical manufacturing.

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What cities are hiring for Assistant Cleaning Validation Engineer jobs? Cities with the most Assistant 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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Assistant Cleaning Validation Engineer jobs near you
Infographic showing various Assistant Cleaning Validation Engineer job openings in the United States as of May 2026, with employment types broken down into 76% Full Time, and 24% Part Time. Highlights an 73% Physical, and 27% Remote job distribution, with an average salary of $88,754 per year, or $42.7 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 6 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.