ZipRecruiter

Log In

1

Cleaning Validation Jobs (NOW HIRING)

Alliance Biotech Solutions LLC

Validation Engineer

Raleigh, NC · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Cleaning Validation Engineer will work cross-functionally with Manufacturing, Quality, Quality Control and Engineering teams to support the cleaning validation, including cycle development, hold ...

3B Staffing LLC

Validation Engineer

Mount Prospect, IL · On-site

Validation Engineer Coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning development and validation. Perform investigation of deviations / discrepancies.

3B Staffing LLC

Validation Engineer

Mount Prospect, IL · On-site

Validation Engineer Coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning development and validation. Perform investigation of deviations / discrepancies.

Bachem

Validation Engineer

Vista, CA · On-site

$103K - $142K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Perform, coordinate, execute and analyze cleaning recovery studies. * Lead cross-functional project teams to address issues and ensure on-time completion of all qualification / validation ...

Agilent

Validation Engineer

Boulder, CO · On-site

This position will be focused on the field of cleaning validation, specifically supporting laboratory studies including method verification, cleanability studies, and surface recovery to aid in MACO ...

Agilent

Validation Engineer

Frederick, CO · On-site

This position will be focused on the field of cleaning validation, specifically supporting laboratory studies including method verification, cleanability studies, and surface recovery to aid in MACO ...

previous pagenext page

Showing results 21-40

All JobsCleaning Validation Jobs

Cleaning Validation information

See salary details

$36

$39

$42

How much do cleaning validation jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for cleaning validation in the United States is $39.42, according to ZipRecruiter salary data. Most workers in this role earn between $37.98 and $40.87 per hour, depending on experience, location, and employer.

What is the job description of cleaning validation?

Cleaning validation is a process used in pharmaceutical and manufacturing industries to ensure that cleaning procedures effectively remove contaminants from equipment and surfaces. The job involves developing, executing, and documenting validation protocols, performing residue testing, and ensuring compliance with regulatory standards. Skills in analytical testing, attention to detail, and knowledge of Good Manufacturing Practices (GMP) are essential for this role.

What is the difference between Cleaning Validation vs Microbiologist?

AspectCleaning ValidationMicrobiologist
Required credentialsGMP, GMP-related certifications, technical trainingBiology, microbiology degrees, certifications
Work environmentPharmaceutical, biotech manufacturing facilitiesLaboratories, research facilities, healthcare settings
Employer and industry usagePharmaceutical, biotech, food industriesHealthcare, research, environmental testing

Cleaning Validation focuses on ensuring that cleaning processes effectively remove contaminants from equipment, primarily in manufacturing settings. Microbiologists study microorganisms, their behaviors, and control methods, often working in labs. While both roles require scientific knowledge and certifications, Cleaning Validation specialists concentrate on process validation in production environments, whereas Microbiologists focus on microbial analysis and research.

How do you become a cleaning validation consultant?

To become a cleaning validation consultant, professionals typically need a background in pharmaceutical or biotech manufacturing, quality assurance, or related fields, along with knowledge of validation processes and regulatory requirements such as FDA or EMA guidelines. Gaining experience through roles in validation, quality control, or manufacturing, and obtaining certifications like ASQ Certified Quality Auditor or specific validation training, can enhance credibility. Strong analytical skills, attention to detail, and familiarity with cleaning procedures and documentation are essential for success in this role.

What does cleaning validation do?

Cleaning validation is a process used in quality assurance roles to ensure that cleaning procedures effectively remove contaminants from equipment, preventing cross-contamination and ensuring product safety. It involves testing and documenting cleaning processes, often requiring knowledge of regulatory standards and analytical methods. Proper cleaning validation helps maintain compliance and product quality in regulated industries.
More about Cleaning Validation jobs
What cities are hiring for Cleaning Validation jobs? Cities with the most Cleaning Validation job openings:
What states have the most Cleaning Validation jobs? States with the most job openings for Cleaning Validation jobs include:
What job categories do people searching Cleaning Validation jobs look for? The top searched job categories for Cleaning Validation jobs are:
Cleaning Validation jobs near you
Infographic showing various Cleaning Validation job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 66% Full Time, 30% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 100% Physical job distribution, with an average salary of $82,000 per year, or $39.4 per hour.

Validation Specialist (Cleaning-In-Place)

Validation & Engineering Group Inc.

Juana Diaz, PR • On-site

Full-time

Re-posted 24 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:

  • Bachelors degree in Chemical, Mechanical, or Biochemical Engineering (or equivalent).
  • Minimum 710 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.

Apply