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Cleaning Validation Jobs (NOW HIRING)

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 ...

kindeva

Validation Engineer II

Maryland Heights, MO · On-site

This role assists with equipment qualification, aseptic process validation, cleaning validation, computer systems validation, and inspection/packaging validation activities. The position delivers ...

kindeva

Validation Engineer II

Maryland Heights, MO · On-site

This role assists with equipment qualification, aseptic process validation, cleaning validation, computer systems validation, and inspection/packaging validation activities. The position delivers ...

kindeva

Validation Engineer II

Maryland Heights, MO · On-site

This role assists with equipment qualification, aseptic process validation, cleaning validation, computer systems validation, and inspection/packaging validation activities. The position delivers ...

Actalent

Validation Specialist

Boca Raton, FL · On-site

$36.06 - $45.67/hr

Execute process validations, media fills, cleaning validations, and requalification activities to ensure ongoing compliance and process robustness. * Conduct risk assessments related to validation ...

BioPhase Solutions

Validation Engineer

Los Angeles, CA

$115K/yr

Execute Process Validation and Cleaning Validation: Identify critical process parameters, establish validation protocols, and conduct cleaning validations to maintain product quality and regulatory ...

PCI Pharma Services

Director, Validation

Bedford, NH · On-site

Direct and manage all aseptic and non-aseptic validation activities, including process validation, cleaning validation, sterilization validation, and equipment qualification. * Maintain ownership and ...

Catalent, Inc.

Validation Engineer

Chelsea, MA · On-site

$89K - $110K/yr

Provide technical support to key site programs, including the cleaning program (cleaning validation ... cleaning chemistry, and master plan) and Continued/Continuous Process Verification (CPV) * Serve as ...

JobRx, Inc.

Director, Validation

Bedford, NH · On-site

$120 - $160/hr

Direct and manage all aseptic and non-aseptic validation activities, including process validation, cleaning validation, sterilization validation, and equipment qualification. * Maintain ownership and ...

Novartis

Validation Lead

Durham, NC

$126K - $234K/yr

Lead the site validation strategy across process, cleaning, packaging, and ongoing process and cleaning verification activities. * Own and maintain the Validation Master Plan, ensuring timely ...

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Cleaning Validation information

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$36

$39

$42

How much do cleaning validation jobs pay per hour?

As of Aug 14, 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.
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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.

Process & Cleaning Validation Specialist, Technical Services

Amneal Pharmaceuticals

Piscataway, NJ • On-site

$80K - $90K/yr

Full-time

Medical, Retirement

This job post has expired 1 day ago. Applications are no longer accepted.

Amneal Pharmaceuticals rating

6.7

Company rating: 6.7 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

74th of 86 rated pharmaceutical

Job description


Description:
Process Engineer reports to the Manager of Technical Services and plans, executes and functionally directs Process/Cleaning Validation/Study assignments and projects, which require sound pharmaceutical/engineering skills and independent judgment. Works as a team member, educates internal partners on the projects, monitors and executes. Maintains effective and cooperative relationships with all departments within and outside the organization. Managing the post approval projects.
Essential Functions:
  • Prepare validation protocols & reports for manufacturing process and cleaning process qualification, data analysisand prepare reports; execute the manufacturing process and cleaning process qualification/validation/study.
  • Managing the post approval projects. coordinating with cross functional Teams and ensuring the timely completion of projects.
  • Analyzes statistical data, products or functional specifications to determine conformance with standards andestablished quality requirements
  • Coordinate/oversee the development of new processes or troubleshoot existing ones
  • Assist in deviation/investigations to identify root causes and define corrective and/or preventative actions (CAPA) & assist in various audits

Additional Responsibilities:
  • Initiation of Change Controls and Planned Deviations when required

Qualifications
Education:
  • Bachelors Degree (BA/BS) Pharmaceutical/Biomedical Engineering - Required
  • Master Degree (MS/MA) Pharmaceutical/Biomedical Engineering - Preferred

Experience:
  • 2 years or more in Pharmaceutical/Manufacturing Industry

Skills:
  • Excellent verbal and written communication skills - Advanced
  • Proficiency in MS Word/Excel/ PowerPoint/MS project - Advanced

Specialized Knowledge:
  • Basic Analytical Knowledge desirable. In-depth knowledge of manufacturing equipment and processes for Solid Oral, Medical Device, Transdermal, Topical and Liquid Orals.

The base salary for this position ranges from $80,000 to $90,000 per year. Amneal ranges reflect the Company's good faith estimate of base salary that Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that helps you enjoy your career alongside life's many other commitments and opportunities.

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