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Cleaning Validation Consultant Jobs (NOW HIRING)

Pharma Bioserv

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Cleaning Validation Consultant

Juncos, PR · On-site

Currently, we are seeking for Cleaning Validation Consultant (SME) available for Puerto Rico or Costa Rica. * Bachelor's degree, with a minimum of 5 - 10 years of relevant experience. * Experience ...

Valspec

CQV Consultant - California

Oceanside, CA · On-site

$65 - $75/hr

Senior Validation Engineer (CQV) -- Equipment & Cleaning Validation Join a leading biopharmaceutical manufacturer in the San Diego area as a Senior Validation Engineer supporting equipment and ...

Valspec

CQV Consultant - California

San Diego, CA · On-site

$65 - $75/hr

Senior Validation Engineer (CQV) -- Equipment & Cleaning Validation Join a leading biopharmaceutical manufacturer in the San Diego area as a Senior Validation Engineer supporting equipment and ...

Intellectt INC

CQV Consultant

Los Angeles, CA · On-site

CQV Consultant Location: Los Angeles, CA Job Summary: We're looking for a Facilities CQV ... Cleaning Validation is highly preferred (to provide backup support as needed). Day-to-day ...

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 ...

Actalent

Validation Engineer

Paramus, NJ

Create, implement, and refine cleaning and disinfection protocols that support consistent ... Ability to work effectively with external consulting firms and integration partners on complex ...

Actalent

Validation Engineer

Paramus, NJ

Create, implement, and refine cleaning and disinfection protocols that support consistent ... Ability to work effectively with external consulting firms and integration partners on complex ...

Automated Systems, Inc.

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Equipment Validation Engineer

Tampa, FL · On-site

$45 - $65/hr

... and cleaning validation studies in accordance with site procedures and industry standards. · ... Company Description We are a dynamic, project oriented consulting company offering individuals a ...

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Cleaning Validation Consultant information

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How much do cleaning validation consultant jobs pay per hour?

As of Aug 3, 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 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 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 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.

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.

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Cleaning Validation Consultant jobs near you
Infographic showing various Cleaning Validation Consultant job openings in the United States as of July 2026, with employment types broken down into 61% Full Time, 38% Part Time, and 1% Temporary. Highlights an 100% Physical job distribution, with an average salary of $82,000 per year, or $39.4 per hour.

Cleaning Validation Consultant

Pharma Bioserv

Juncos, PR • On-site

Contractor

Posted 6 days ago

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Job description

Pharma-Bio Serv, a global consulting firm headquartered in Puerto Rico, has been dedicated exclusively to providing services to the largest biotechnology & bio-engineering companies within the regulated industry for over 30 years. Since our inception, our services have resulted in project experience level and personnel resource base ranking among the highest worldwide.


Currently, we are seeking for Cleaning Validation Consultant (SME) available for Puerto Rico or Costa Rica.


  • Bachelor’s degree, with a minimum of 5 - 10 years of relevant experience.
  • Experience developing and executing cleaning validation and the applicable technical documentation (cleaning process design (development), performance qualification (PQ) and continued process verification (CPV) ).
  • Develop technical documentation such as cleaning validation plans, development protocols, risk assessments, validation protocols, sampling strategy, procedures, cleaning instructions, among others.
  • Skilled determining the acceptance criteria applicable for cleaning (micro, cleaning agent, API, as applicable).
  • Fully bilingual - Spanish & English


This position does not offer visa sponsorship. Applicants must be fluent in both Spanish and English. Please do not apply if you do not meet these requirements.

Company Description

Pharma-Bio Serv, a global consulting firm headquartered in Puerto Rico, has been dedicated exclusively to providing services to the largest biotechnology & bio-engineering companies within the regulated industry for more than 30 years. Since our inception, our services have resulted in a project experience level and personnel resource base ranking among the highest worldwide.