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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 ... * Assist in managing deviations, non-conformances, and change controls related to CIP/SIP systems.

Catalent, Inc.

Validation Engineer

Chelsea, MA · On-site

$89K - $110K/yr

The Validation Engineer is responsible for executing validation activities within a GMP ... Provide technical support to key site programs, including the cleaning program (cleaning validation ...

Catalent Pharma Solutions

Validation Engineer

Chelsea, MA · On-site

$89K - $110K/yr

The Validation Engineer is responsible for executing validation activities within a GMP ... Provide technical support to key site programs, including the cleaning program (cleaning validation ...

Sebela Pharma

CQV/Validation Engineer

Holbrook, MA · On-site

$33 - $43/hr

The CQV/Validation Engineer is responsible for supporting the activities required to implement the ... cleaning, and computerized system validation activities, as assigned. * Document and assist in ...

INCOG

Senior Validation Engineer

Fishers, IN

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

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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 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.
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What cities are hiring for Assistant Cleaning Validation Engineer jobs? Cities with the most Assistant Cleaning Validation Engineer job openings:
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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 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.

Validation Specialist (Cleaning-In-Place)

Validation & Engineering Group, Inc

PR

Full-time

Re-posted 26 days ago

Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • Validation Specialist - CIP

Summary:
The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and Sterilization-In-Place (SIP) systems within a biotech manufacturing environment. This role ensures that cleaning and sterilization systems are installed, tested, and qualified in compliance with GMP, FDA, EMA, and ASTM E2500 standards, supporting readiness for process validation and commercial manufacturing.

Key Responsibilities:
Commissioning & Qualification Execution:

  • Review and approve vendor FAT/SAT protocols for CIP/SIP equipment.
  • Execute IOQ and PQ protocols for CIP/SIP systems, including cleaning recipe verification, steam sterilization cycle qualification, and temperature mapping.
  • Oversee the qualification of utilities supporting CIP/SIP systems (Clean Steam, WFI, Process Air).
  • Collaborate closely with Automation, Process, and QA Validation for recipe verification and data integrity.


Documentation & Compliance:

  • Generate and review URS, FAT/SAT, IOQ, and PQ documentation in compliance with ASTM E2500 and GAMP 5.
  • Ensure traceability from design specifications through executed testing.
  • Assist in managing deviations, non-conformances, and change controls related to CIP/SIP systems.
  • Prepare summary reports for Quality Assurance approval.


Cross-functional Collaboration:

  • Collaborate with Process Engineers, Automation, QA, and Manufacturing to ensure successful integration of CIP/SIP operations with process equipment.
  • Support operations during process validation batches and cleaning validation campaigns.
  • Provide training and technical guidance to CQV engineers and contractors executing test protocols.


Qualifications:

  • Bachelor’s degree in Chemical, Mechanical, or Biochemical Engineering (or equivalent).
  • Minimum 7–10 years of experience in CQV within biotech or pharmaceutical manufacturing environments.
  • Experience in generating and executing documentation for CQV activities.
  • Strong knowledge of cleaning validation, sterilization principles, and automation integration.
  • Familiarity with DeltaV, SCADA, or PLC systems for CIP/SIP recipe management.
  • Expertise in ASTM E2500, ISPE Baseline Guides, GAMP 5, and FDA/EMA guidelines.
  • Proficiency in reviewing P&IDs, piping isometrics, and functional design specifications.
  • Experience executing or overseeing FAT/SAT, IOQ, PQ activities.
  • Knowledge of data integrity, 21 CFR Part 11, and electronic validation systems (e.g., Kneat, ValGenesis).
  • Must be fully bilingual (English / Spanish) with excellent oral skills.
  • Available to work extended hours, possibility of weekends and holidays.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.