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Assistant Cleaning Validation Engineer Jobs (NOW HIRING)

Moriah Engineering

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 ...

BioPhase Solutions

Validation Engineer

Los Angeles, CA

$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 ...

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 ...

Stark Pharma Solutions Inc

IL · On-site

Maintain validation lifecycle documentation and ensure all records are audit-ready. * Assist with ... Familiarity with computerized systems validation (CSV), cleaning validation, or utility ...

Actalent

Validation Engineer

Paramus, NJ

Validation Engineer This role focuses on developing and executing validation, cleaning, and environmental control strategies within regulated cleanroom manufacturing operations. The Validation ...

Actalent

Validation Engineer

Paramus, NJ

Validation Engineer This role focuses on developing and executing validation, cleaning, and environmental control strategies within regulated cleanroom manufacturing operations. The Validation ...

Pharma Bioserv

Be Seen First

Cleaning Validation Consultant

Juncos, PR · On-site

... engineering companies within the regulated industry for over 30 years. Since our inception, our ... Currently, we are seeking for Cleaning Validation Consultant (SME) available for Puerto Rico or ...

Automated Systems, Inc.

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Equipment Validation Engineer

Tampa, FL · On-site

$45 - $65/hr

... and cleaning validation studies in accordance with site procedures and industry standards. · ... Engineering, Pharmacy, Science, or a related technical discipline. · Two or more years of ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Perform risk assessments to support cleaning validation strategies ... Collaborate with Quality, Manufacturing, Engineering, Validation, and Microbiology teams. * Analyze ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Perform risk assessments to support cleaning validation strategies ... Collaborate with Quality, Manufacturing, Engineering, Validation, and Microbiology teams. * Analyze ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Perform risk assessments to support cleaning validation strategies ... Collaborate with Quality, Manufacturing, Engineering, Validation, and Microbiology teams. * Analyze ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Perform risk assessments to support cleaning validation strategies ... Collaborate with Quality, Manufacturing, Engineering, Validation, and Microbiology teams. * Analyze ...

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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 Aug 6, 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.

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, 76% Full Time, 20% Part Time, 1% Temporary, and 2% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $88,754 per year, or $42.7 per hour.

Validation Engineer IV

Quality Agents, LLC

Rockville, MD • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 25 days ago

Job description

Quality Agents, LLC is a service company offering validation and quality expertise to the pharmaceutical and biotechnology industries. Our Validation Engineers will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The Validation Engineer will evaluate the equipment/utility/system/procedures used in development, production, and holding of pharmaceutical products and determine a validation approach. The individual should have experience with current US and international regulations, guidance, industry best practice in one of the following areas of validation: facilities, utilities, and equipment qualifications, process validation, analytical method validation, or 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.
Responsibilities include:
  • Interact with clients and works closely with site manufacturing, engineering, and QA to develop validation documents.
  • Travel to various client sites and work independently to complete tasks.
  • Provide qualification and validation services for cGMP manufacturing equipment, systems, and utilities at client sites.
  • Exposure to validation aspects of facility start-up, redesign/retrofit, and expansion.
  • Writes and executes qualification protocols for a variety of biopharmaceutical equipment and support utilities in accordance with SOPs, master plans, regulatory expectations, and industry standards.
  • Conducts temperature mapping studies, including the operation of Kaye dataloggers, or equivalent.
  • Review and approve documented test results and maintain records for later analysis.
  • Assist with non-conformances, investigations, and troubleshooting of equipment, utilities, and systems.
  • Able to read P&IDs, isometric drawings, and As-built drawings.

Skill Level and Requirements:
  • Ability to problem solve and troubleshoot.
  • Technical writing ability and use of Microsoft Word, Excel, Power point, and Project
  • Experience with validation equipment such as the Kaye validator, wireless data loggers, or other monitoring devices is strongly desired.
  • Experience using statistical tools is a plus to analyze data captured during validation studies.

Minimum Requirements:
  • BS in a technical discipline (Engineering, chemistry, microbiology, biology)
  • 7+ years of experience in at least one of the following areas: equipment/utility qualifications, process validation, analytical method validation, or cleaning validation.
  • Current driver's license and auto insurance

Quality Agents offers a full suite of benefits for full-time employees including:
  • Health, dental and vision insurance
  • Life, AD&D and disability Insurance
  • Health savings account for participants in our health plan
  • 401k retirement plan
  • Paid time off
  • Paid holidays

Quality Agents accepts applications on an on-going basis in order to build a talent pool of potential candidates. These applications remain open for consideration, as positions become available, for one (1) year from the date of application. After that time, or if your application information changes, please submit your application again.

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