ZipRecruiter

Log In

1

Assistant Cleaning Validation Engineer Jobs (NOW HIRING)

Validation & Engineering Group, Inc

PR

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Cleaning Validation Specialist We are looking for a resource to support the development and ...

Validation & Engineering Group, Inc

PR

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 ...

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

Author and execute validation protocols and reports * Assist in process validation (PPQ ... Cleaning validation experience * Exposure to PPQ * Utilities/facility qualification experience

Intellectt INC

"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 ...

Intellectt INC

Validation Engineer

San Diego, CA · On-site

Validation Engineer Location: San Diego, CA Duration: Longterm Job Summary: A Validation Engineer ... Execute validation protocols for equipment qualification, process validation, cleaning validation ...

next page

Showing results 1-20

All JobsCleaning Validation Engineer JobsAssistant Cleaning Validation Engineer Jobs

Assistant Cleaning Validation Engineer information

See salary details

$33K

$88.8K

$134.5K

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

As of Jul 15, 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.

How much does a validation engineer make at Pfizer?

A validation engineer at Pfizer typically earns between $70,000 and $100,000 annually, depending on experience, location, and certifications. The role involves ensuring compliance with industry standards and often requires knowledge of validation protocols and regulatory requirements.

Are validation engineers in demand?

Validation engineers, including those specializing in cleaning validation, are in demand across industries such as pharmaceuticals and biotechnology due to strict regulatory requirements. Their expertise in validation protocols, compliance standards, and quality assurance makes them valuable, especially as companies prioritize product safety and regulatory adherence.

What does a cleaning validation engineer do?

A cleaning validation engineer is responsible for developing, executing, and documenting cleaning procedures to ensure pharmaceutical or manufacturing equipment is free of contaminants. They verify that cleaning processes meet regulatory standards, often using analytical tools and validation protocols, to maintain product safety and quality. This role requires attention to detail, knowledge of GMP regulations, and often involves working with cross-functional teams during audits and inspections.

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.

What is the hourly rate for product validation expert?

The hourly rate for a product validation expert, including assistant cleaning validation engineers, typically ranges from $30 to $60 depending on experience, location, and industry. Certified professionals with specialized skills may command higher rates, especially in regulated environments like pharmaceuticals or biotech. Rates can vary based on project complexity and whether the work is freelance or employed full-time.
More about Assistant Cleaning Validation Engineer jobs
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:
What states have the most Assistant Cleaning Validation Engineer jobs? States with the most job openings for Assistant Cleaning Validation Engineer jobs include:
What job categories do people searching Assistant Cleaning Validation Engineer jobs look for? The top searched job categories for Assistant Cleaning Validation Engineer jobs are:
Assistant Cleaning Validation Engineer jobs near you
Infographic showing various Assistant Cleaning Validation Engineer job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 75% Full Time, 21% Part Time, 1% Temporary, and 2% Contract. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $88,754 per year, or $42.7 per hour.

Cleaning Validation Engineer

Eliquent Life Sciences, Inc

Montrose, CA • On-site

Full-time

Posted 21 days ago

Job description

About Company:

Who Are We?

ELIQUENT Life Sciences is a leading global consulting group delivering regulatory affairs, pharmacovigilance, quality, and compliance solutions that support pharmaceutical, biotechnology, medical device, and combination product companies across therapeutic modalities, phase-based pathways, and major global markets.


Why explore your future at ELIQUENT?

ELIQUENT Life Sciences is a trusted global consulting firm helping life sciences companies navigate regulatory complexity and bring breakthrough therapies to market. Founded by former regulators and industry experts, we offer end-to-end support in regulatory affairs, pharmacovigilance, and quality compliance. Our team is driven by a shared mission to improve global health through innovation, collaboration, and integrity. At ELIQUENT, you will be part of a purpose-led organization where your expertise contributes to meaningful impact and your growth is supported every step of the way.


About the Role:

The Cleaning Validation Engineer plays a critical role in ensuring that pharmaceutical manufacturing equipment and processes meet stringent cleanliness standards to guarantee product safety and regulatory compliance. This position is responsible for designing, executing, and maintaining cleaning validation protocols that confirm the effective removal of contaminants and residues from manufacturing systems. The engineer collaborates closely with cross-functional teams including quality assurance, production, and engineering to develop scientifically sound validation strategies aligned with industry best practices and regulatory requirements. By analyzing data and continuously improving cleaning processes, the role helps to minimize risks of cross-contamination and supports the overall integrity of pharmaceutical products. Ultimately, the Cleaning Validation Engineer ensures that all cleaning activities are validated, documented, and compliant with FDA, EMA, and other relevant regulatory bodies, thereby safeguarding patient health and company reputation.

Minimum Qualifications:

  • Bachelor’s degree in Pharmaceutical Engineering, Chemical Engineering, or a related scientific discipline.
  • Demonstrated experience in cleaning validation within pharmaceutical manufacturing environments.
  • Strong knowledge of Sterilize-In-Place (SIP) systems and pharmaceutical manufacturing processes.
  • Familiarity with regulatory requirements such as FDA, EMA, and ICH guidelines related to cleaning validation.
  • Proficiency in developing and executing validation protocols and technical reports.

Preferred Qualifications:

  • Advanced degree (Master’s or higher) in Pharmaceutical Engineering or related field.
  • Experience with automation and control systems used in pharmaceutical manufacturing.
  • Certification in validation or quality assurance (e.g., ASQ Certified Quality Engineer).
  • Hands-on experience with analytical techniques such as HPLC, TOC, or ATP bioluminescence for cleaning verification.
  • Strong project management skills and experience leading cross-functional validation projects.

Responsibilities:

  • Develop, review, and execute cleaning validation protocols and reports in accordance with cGMP and regulatory guidelines.
  • Perform risk assessments and establish acceptance criteria for cleaning processes based on product and equipment characteristics.
  • Collaborate with manufacturing and quality teams to identify critical cleaning parameters and optimize cleaning procedures.
  • Conduct sampling, analytical testing, and data analysis to verify the effectiveness of cleaning processes.
  • Maintain comprehensive documentation and ensure all validation activities are audit-ready and compliant with regulatory standards.
  • Investigate and resolve deviations or non-conformances related to cleaning validation activities.
  • Stay current with industry trends, regulatory changes, and emerging technologies to continuously improve cleaning validation practices.

Skills:

The required skills such as expertise in SIP systems and pharmaceutical manufacturing processes are applied daily to design and optimize cleaning validation protocols that ensure equipment cleanliness and product safety. Pharmaceutical engineering knowledge enables the engineer to understand complex manufacturing systems and develop scientifically robust validation strategies. Analytical skills are essential for interpreting test results and making data-driven decisions to improve cleaning procedures. Preferred skills like familiarity with advanced analytical techniques and automation systems enhance the engineer’s ability to implement innovative solutions and increase validation efficiency. Effective communication and project management skills facilitate collaboration with multidisciplinary teams and ensure timely completion of validation projects in compliance with regulatory standards.