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Cleaning Validation Consultant Jobs (NOW HIRING)

Inc. (Vti)

Cleaning Validation Engineers

Glendale, CA · On-site

$80 - $110/hr

... consulting with some of the biggest companies in the Life Sciences industry. We are currently ... Job Title Cleaning Validation Engineer Industry Biotechnology Level of Experience 4+ years Location ...

Penn Life Sciences

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Manager, Facilities & Engineering (Validation)

Langhorne, PA · On-site

$130K - $150K/yr

Support process validation, cleaning validation, sterilization validation, aseptic process ... Experience managing capital projects, engineering contractors, validation consultants, budgets ...

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How much do cleaning validation consultant jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for cleaning validation consultant 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 a cleaning validation consultant?

Cleaning Validation Consultants are specialized professionals who help organizations in regulated industries, such as pharmaceuticals and biotechnology, ensure their cleaning processes meet regulatory standards. They design, implement, and review cleaning validation protocols to confirm that manufacturing equipment is free from contaminants, residues, and cross-contamination risks. These consultants provide expertise in compliance, documentation, risk assessment, and troubleshooting to help companies pass regulatory inspections. Their work is essential for maintaining product quality and patient safety.

What does a cleaning validation consultant do?

Your job duties as a cleaning validation consultant revolve around helping pharmaceutical companies clean equipment and remove residue from surfaces after production runs for pharmaceutical products. Your responsibilities include inspecting equipment and assisting manufacturers to prevent cross-contamination. You provide advice on how to improve their purification process in a way that does not interfere with the chemical makeup of their medicines. You may help companies establish clean-in-place (CIP) or sterilization-in-place (SIP) procedures. You test these procedures and approve, alter, or enhance them based on your findings.

What are the key skills and qualifications needed to thrive as a cleaning validation consultant, and why are they important?

To thrive as a Cleaning Validation Consultant, you need a strong background in pharmaceutical manufacturing processes, regulatory compliance (such as FDA or EMA guidelines), and a relevant science or engineering degree. Familiarity with validation protocols, analytical testing instruments (like HPLC or TOC analyzers), and documentation systems is essential. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These skills ensure cleaning processes meet regulatory standards, minimize contamination risks, and support efficient audits and inspections.

What are the common challenges faced by cleaning validation consultants when working with multiple manufacturing sites?

Cleaning Validation Consultants often navigate varying equipment, protocols, and regulatory interpretations across multiple manufacturing sites. Adapting cleaning strategies to diverse product mixes and legacy systems can be complex, requiring strong analytical and communication skills. Consultants must also harmonize documentation and ensure alignment with global regulatory standards while collaborating closely with site teams, making adaptability and attention to detail essential in this role.
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Cleaning Validation Consultant jobs near you
Infographic showing various Cleaning Validation Consultant job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 64% Full Time, 32% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $82,000 per year, or $39.4 per hour.

Cleaning Validation Subject Matter Expert

cGMP Consulting

North Chicago, IL • On-site

$120 - $160/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 5 days ago

Job description

About Us

At cGMP Consulting, we specialize in providing expert validation, qualification, and compliance services to the life sciences industry. Our team works with clients to ensure their facilities, equipment, and processes meet regulatory standards, enabling the safe and efficient production of pharmaceuticals.
cGMP Consulting is based in Lake Forest, IL. Our main client locations are Melrose Park, IL, North Chicago, IL, Waukegan, IL and Pleasant Prairie, WI.

Position Summary

cGMP Consulting is seeking an experienced and driven individual to lead and manage cleaning validation activities, prepare and execute protocols, and act as SME regarding cleaning development and validation. This senior-level role offers significant autonomy, leadership responsibility, and the opportunity to influence operations in a fast-paced, GMP-compliant manufacturing environment.

The ideal candidate will have a proven ability to lead cross-functional initiatives, navigate complex troubleshooting challenges, drive change management efforts, and ensure timely and thorough completion of protocols. This candidate has deep experience in current Good Manufacturing Practices (cGMP), along with a solid understanding of FDA regulations, and international compliance standards.

Responsibilities

The essential functions include, but are not limited to the following:

  • Design and develop cleaning procedures for new product and manufacturing equipment.
  • Provide technical support to cleaning activities associated with the manufacturing process.
  • Lead the cleaning validation program and activities.
  • Knowledge of cleaning agents and establishment of sound cleaning practices within new or refurbished manufacturing rooms and sampling suite areas.
  • Design and support implementation of cleaning strategies for product transfer projects and product development projects.
  • Investigate and conduct troubleshooting or root cause analysis of cleaning related incidents, deviations and cleaning out of specificationresults for non validated or under developed cleaning procedures.
  • Lead enhancement of cleaning practices and review and approve work instructions.
  • Support the periodic review of cleaning validation studies.
  • Perform successful resolution of incidents and deviations related to cleaning activities.
  • Issue change controls required for implementation of cleaning procedure changes.
Requirements
  • Minimum Bachelors’ degree in Engineering, Science, or a related field of study.
  • 4+ years’ experience in a GMP manufacturing environment, including cleaning validation. Must be familiar with regulatory (FDA) requirements.
  • Expertise in multipleareas: cleaning validation, continuous process improvement, and/or qualification of aseptic filling or formulation equipment/processes.
  • Advanced critical thinking and technical writing skills.
  • Strong organizational, communication, and interpersonal skills.
Compensation and Benefits
  • Expected pay range per year: $120,000-$160,000 USD
  • Expected benefits include: Medical, Dental, Vision, PTO, 401K
Disclaimer

The duties and responsibilities described are not a comprehensive list and additional tasks may be assigned to the employee from time to time; or the scope of the job may change as necessitated by business demands. All duties and responsibilities are subject to possible modification to reasonably accommodate individuals with disabilities. The requirements listed are the minimum levels of knowledge, skills, or abilities necessary to perform this job successfully. The company is an Equal Opportunity Employer, drug-free workplace, and complies with ADA regulations as applicable.

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