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 ...
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 ...
Validation Engineer II
Bothell, WA · On-site
Validation Engineer II (Onsite) Location: Bothell, WA Overview: We are looking for a CQV ... Cleaning validation experience * Exposure to PPQ * Utilities/facility qualification experience
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Validation Engineer II
Bothell, WA · On-site
Validation Engineer II (Onsite) Location: Bothell, WA Overview: We are looking for a CQV ... Cleaning validation experience * Exposure to PPQ * Utilities/facility qualification experience
"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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"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 ...
Validation Engineer IV
Rockville, MD · On-site
... 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.
Validation Engineer IV
Rockville, MD · On-site
... 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.
Validation Engineer II
Rockville, MD · On-site
... 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.
Validation Engineer II
Rockville, MD · On-site
... 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.
Validation Engineer
Los Angeles, CA · On-site
$115K/yr
Execute Process Validation and Cleaning Validation: Identify critical process parameters, establish ... Bachelors in engineering, chemistry, or related field * Certifications related to GMP compliance ...
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Validation Engineer
Los Angeles, CA · On-site
$115K/yr
Execute Process Validation and Cleaning Validation: Identify critical process parameters, establish ... Bachelors in engineering, chemistry, or related field * Certifications related to GMP compliance ...
Senior Validation Engineer / Manager Location: Seattle, WA (100% On-site) Duration: 6 Months (High ... Cleaning Validation * Utilities Validation (PW, WFI, HVAC, Compressed Air) * Equipment ...
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Senior Validation Engineer / Manager Location: Seattle, WA (100% On-site) Duration: 6 Months (High ... Cleaning Validation * Utilities Validation (PW, WFI, HVAC, Compressed Air) * Equipment ...
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 ...
Quick apply
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 ...
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 ...
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 ...
Cleaning Validation Specialist
Jayuya, 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 ...
Cleaning Validation Specialist
Jayuya, 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 ...
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 ...
Quick apply
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 ...
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 ...
Quick apply
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 ...
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 ...
Quick apply
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 ...
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 ...
Quick apply
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 ...
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 ...
Quick apply
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 ...
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 ...
Quick apply
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 ...
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 ...
Quick apply
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 ...
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 ...
Quick apply
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 ...
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 ...
Quick apply
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 ...
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 ...
Quick apply
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 ...
Cleaning Validation Engineer information
See salary details
$22.60 - $27.64
2% of jobs
$27.64 - $32.69
6% of jobs
$32.69 - $37.74
13% of jobs
$39.32 is the 25th percentile. Wages below this are outliers.
$37.74 - $42.79
13% of jobs
$42.79 - $47.84
11% of jobs
The median wage is $50.36 / hr.
$47.84 - $52.88
12% of jobs
$52.88 - $57.93
9% of jobs
$61.82 is the 75th percentile. Wages above this are outliers.
$57.93 - $62.98
13% of jobs
$62.98 - $68.03
13% of jobs
$68.03 - $73.08
6% of jobs
$73.08 - $78.13
3% of jobs
$22
$51
$78
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.
More about Cleaning Validation Engineer jobs
What cities are hiring for Cleaning Validation Engineer jobs? Cities with the most 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:
What states have the most Cleaning Validation Engineer jobs? States with the most job openings for Cleaning Validation Engineer jobs include:
What job categories do people searching Cleaning Validation Engineer jobs look for? The top searched job categories for Cleaning Validation Engineer jobs are:
Other
Posted 3 days ago
Kindeva rating
6.8
Based on 6 frontline employees who took The Breakroom Quiz
Job description
Our Work Matters
At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.
The Impact You Will Make
The Floater Validation Engineer II provides validation engineering support across two pharmaceutical aseptic manufacturing facilities and one inspection and packaging site. This role assists with equipment qualification, aseptic process validation, cleaning validation, computer systems validation, and inspection/packaging validation activities. The position delivers flexible, cross-site validation coverage while executing protocols, performing testing, and authoring validation documentation under the direction of the Validation Manager.
Responsibilities
• Provide validation support across multiple sites based on business priorities.
• Assist in equipment qualification (IQ/OQ/PQ), cleaning validation, process validation, and CSV.
• Execute and author validation protocols and reports.
• Support aseptic manufacturing and inspection/packaging validation activities.
• Issue validation data, protocols, reports, and technical memos.
• Support site change management programs and maintain validated states.
• Assist with Validation Master Plans and Continuous Process Verification activities.
• Review vendor turnover packages and User Requirement Specifications.
Qualifications
- Bachelor’s degree in Engineering, Chemistry, Biochemistry, Microbiology, Pharmacy or related discipline
- 5+ years of relevant validation or pharmaceutical manufacturing experience, or equivalent combination of education and experience.
- Knowledge of cGMP and regulatory guidance.
- Experience in aseptic manufacturing and inspection/packaging operations.
- Ability to interpret technical documentation and identify deviations.
• Proficiency with Microsoft Office applications.
- Regular travel between sites required; ability to adapt to multiple GMP environments.
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About Kindeva
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