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Assistant Cleaning Validation Engineer Jobs (NOW HIRING)

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 ...

Performance Validation, Inc

Validation Engineer

Raleigh, NC · On-site

$80K - $83K/yr

About the job Performance Validation is seeking a full-time Level 2 Validation Engineer/Specialist ... Cleaning, Sterlization, and Decontamination Validation experienced preferred * Device Assembly and ...

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 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.

Senior Validation Manager/SME

Intellectt INC

Seattle, WA • On-site

Contractor

Re-posted 13 days ago

Job description

Job Title: Senior Validation Engineer / Validation Manager

Location: Near Seattle, WA (100% Onsite)
Duration: 6 Months Contract (High likelihood of extension or full-time conversion)

Job Summary:

We are seeking an experienced Senior Validation Engineer / Manager to serve as the Site Validation Subject Matter Expert (SME). This is a hands-on leadership role requiring both strategic oversight and execution across multiple validation disciplines. The ideal candidate will be capable of independently driving validation activities, ensuring regulatory compliance, and leading a small team in a fast-paced environment.

Key Responsibilities:

  • Act as the primary Validation SME across all site validation activities
  • Author, review, and approve validation documentation including VMPs, protocols, and reports
  • Ensure compliance with FDA, EU GMP, and ICH regulatory standards
  • Lead, mentor, and manage a team of validation engineers (~3 members)
  • Oversee and coordinate work of external validation contractors
  • Own and manage validation schedules, priorities, and deliverables
  • Identify validation risks and compliance gaps; proactively escalate issues
  • Collaborate cross-functionally with QA, Manufacturing, Engineering, and Regulatory teams
  • Support internal/external audits and regulatory inspections

Required Qualifications:

  • 15+ years of validation experience in Pharma, Biotech, or Medical Device industries
  • Strong expertise in:
    • Cleaning Validation
    • Utilities Validation (PW, WFI, HVAC, Compressed Air)
    • Equipment Qualification (IQ/OQ/PQ)
    • Computer System Validation (CSV – GAMP 5, 21 CFR Part 11)
    • Shipping / Distribution Validation
  • Proven leadership and team management experience
  • Deep understanding of FDA 21 CFR, EU GMP, and ICH guidelines
  • Strong technical writing and documentation skills
  • Experience supporting regulatory inspections and audit readiness
  • Bachelor’s degree required (Advanced degree preferred)