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Cleaning Validation Engineer Jobs (NOW HIRING)

The Senior Validation Engineer is responsible for understanding and implementing validation ... This includes, but is not limited to, clean utilities, autoclave, washer, filler, laboratory ...

Senior Validation Engineer

Plymouth, MN · On-site

$94K - $130K/yr

Process & Cleaning Validation (PQ/PPQ) On average, this will represent about 45% of your time. In ... Mentor junior validation engineers and provide technical guidance on protocol authorship, execution ...

Senior Validation Engineer

Petersburg, VA · On-site

$120K - $150K/yr

The Senior Validation Engineer will support commissioning, qualification, process validation, cleaning validation, and validation lifecycle activities at the Phlow Petersburg Campus. This role ...

Senior Validation Engineer

Petersburg, VA · On-site

$120K - $150K/yr

The Senior Validation Engineer will support commissioning, qualification, process validation, cleaning validation, and validation lifecycle activities at the Phlow Petersburg Campus. This role ...

Validation Engineer Mativ is a global leader in specialty materials headquartered in Alpharetta ... Experience with validation of cleaning, software, automated systems, packaging and laboratory ...

Process & Cleaning Validation (PQ/PPQ) On average, this will represent about 45% of your time. In ... Mentor junior validation engineers and provide technical guidance on protocol authorship, execution ...

Description The Senior Validation Engineer will support commissioning, qualification, process ... Cleaning Validation Develop cleaning validation strategies, protocols, sampling plans, risk ...

$94K - $130K/yr

Process & Cleaning Validation (PQ/PPQ) On average, this will represent about 45% of your time. In ... Mentor junior validation engineers and provide technical guidance on protocol authorship, execution ...

Validation

Boca Raton, FL · On-site

$75K - $95K/yr

The Validation Specialist / Validation Engineer is responsible for planning, executing, documenting ... Clean Steam * Compressed Air * Nitrogen * Environmental Monitoring systems * Execute and/or support ...

Validation Engineer FLSA: Salary Exempt Location: Dallas, Texas Description: The Validation ... Experience with validation of cleaning, software, automated systems, packaging and laboratory ...

Showing results 41-60

Cleaning Validation Engineer information

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How much do cleaning validation engineer jobs pay per hour?

As of Sep 14, 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 is a cleaning validation engineer?

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.

What are the key skills and qualifications needed to thrive as a cleaning validation engineer, 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.

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Infographic showing various Cleaning Validation Engineer job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 62% Full Time, 34% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Senior Validation Engineer

Fishers, IN

INCOG
Public Administration • 51 - 200 employees

Full-time

Re-posted 8 days ago


Job description

INCOG BioPharma is seeking a highly motivated Senior Validation Engineer with validation expertise to join our team. The Senior Validation Engineer is a key individual contributor role within the INCOG BioPharma Validation Department. The Senior Validation Engineer is responsible for understanding and implementing validation requirements for a sterile injectables manufacturing facility. The ideal candidate has subject matter expertise and practical experience in qualification and validation.
The Senior Validation Engineer will partner with internal customers to meet the needs of client projects, facility upgrades, capital expansion projects, and laboratory systems. They will possess a demonstrated ability to influence positive outcome without direct reporting authority.Additionally, they must thoroughly understand and be able to adapt to the changing needs of a manufacturing environment.


Essential Job Functions:

  • Perform Qualification activities on utilities, equipment and laboratory systems. This includes, but is not limited to, clean utilities, autoclave, washer, filler, laboratory instruments, controlled temperature units, etc.
  • Interact with clients to provide validation support including but not limited to, customer product launches, new equipment qualifications.
  • Support and provide validation oversight for capital expansion projects/build outs
  • Take ownership in the development and modification of Standard Operating Procedures (SOPs), Work Instructions (WIs) and guidelines for equipment validation policies, standards, procedures, and templates
  • Review facility changes and provide input on re-validation and re-qualification of equipment
  • Assess risks involved in processing steps related to equipment, developing and/or reviewing validation requirements and design deliverables
  • Engage in a cross functional team and work closely with other supporting groups including Engineering and Operations to support and monitor validation and process improvement efforts
  • Conduct validation qualifications in accordance with all applicable protocols and identify associated protocol excursions.
  • Identify industry trends in validation and expectations of regulatory agencies and propose program modifications as appropriate to align with current requirements.

Special Job Requirements:

  • Bachelor's degree or higher in STEM discipline
  • 5-8 years of experience in Validation or related discipline
  • 4+ years GMP experience required or other regulated industry
  • Physically capable of working onsite

Additional Preferences:

  • Master's degree or higher preferred
  • Computer System Validation experiencepreferred
  • Cleaning Validation experience preferred
  • VHP & Steam Sterilization experience preferred


INCOG is hiring for both Validation Engineer and Senior Validation Engineer opportunities. The final level will be determined based on the candidate's qualifications, relevant industry experience, technical expertise, and demonstrated independence. Candidates may be considered for the Validation Engineer or Senior Validation Engineer level as appropriate.

Additional info about INCOG BioPharma Services:

At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.


If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.


INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.


Qualified applicants must be authorized to work in the United States on a full-time basis. INCOG will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.


By submitting your resume and details, you are declaring that the information is correct and accurate.

Employment Type: Full-Time

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About INCOG

Sourced by ZipRecruiter

Industry

Public administration

Company size

51 - 200 Employees

Headquarters location

Tulsa, OK, US

Year founded

1967