Analyze data and compile conclusions to support validation activities. * Support change controls ... Strong knowledge of cleaning validation principles, including residue limits, risk assessments, and ...
Analyze data and compile conclusions to support validation activities. * Support change controls ... Strong knowledge of cleaning validation principles, including residue limits, risk assessments, and ...
We are looking to fill a Scientist III - Cleaning Validation Analytical Chemist position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in ...
We are looking to fill a Scientist III - Cleaning Validation Analytical Chemist position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in ...
In this role you'll be working with Operations, Quality Assurance, Analytical and Microbiology laboratories, and Validation Engineers to coordinate and facilitate cleaning validation activities. This ...
Quick apply
In this role you'll be working with Operations, Quality Assurance, Analytical and Microbiology laboratories, and Validation Engineers to coordinate and facilitate cleaning validation activities. This ...
A Day in the Life: * ~70% desk-based: protocol writing, data analysis, deviation investigations ... Process validation * Cleaning validation * Equipment qualification (IQ/OQ/PQ) * Support tech ...
A Day in the Life: * ~70% desk-based: protocol writing, data analysis, deviation investigations ... Process validation * Cleaning validation * Equipment qualification (IQ/OQ/PQ) * Support tech ...
A Day in the Life: * ~70% desk-based: protocol writing, data analysis, deviation investigations ... Process validation * Cleaning validation * Equipment qualification (IQ/OQ/PQ) * Support tech ...
A Day in the Life: * ~70% desk-based: protocol writing, data analysis, deviation investigations ... Process validation * Cleaning validation * Equipment qualification (IQ/OQ/PQ) * Support tech ...
Perform data analysis to support validation conclusions * Support change controls, deviations, and ... Strong knowledge of cleaning validation, including residue limits and risk-based approaches
Perform data analysis to support validation conclusions * Support change controls, deviations, and ... Strong knowledge of cleaning validation, including residue limits and risk-based approaches
Perform data analysis to support validation conclusions * Support change controls, deviations, and ... Strong knowledge of cleaning validation, including residue limits and risk-based approaches
Perform data analysis to support validation conclusions * Support change controls, deviations, and ... Strong knowledge of cleaning validation, including residue limits and risk-based approaches
A Day in the Life: * ~70% desk-based: protocol writing, data analysis, deviation investigations ... Process validation * Cleaning validation * Equipment qualification (IQ/OQ/PQ) * Support tech ...
A Day in the Life: * ~70% desk-based: protocol writing, data analysis, deviation investigations ... Process validation * Cleaning validation * Equipment qualification (IQ/OQ/PQ) * Support tech ...
Validation Analyst 3-1
Rockford, IL · On-site
$27.27 - $30.68/hr
The Validation Analyst III is responsible for overall validation project management of large ... and cleaning validation protocols. * Reviews production jacket and issuance to ensure that ...
New
Validation Analyst 3-1
Rockford, IL · On-site
$27.27 - $30.68/hr
The Validation Analyst III is responsible for overall validation project management of large ... and cleaning validation protocols. * Reviews production jacket and issuance to ensure that ...
New
Validation Engineer IV
Rockville, MD · On-site
... validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the ...
Validation Engineer IV
Rockville, MD · On-site
... validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the ...
Validation Analyst 3-1
Rockford, IL · On-site
$27.27 - $30.68/hr
The Validation Analyst III is responsible for overall validation project management of large ... and cleaning validation protocols. * Reviews production jacket and issuance to ensure that ...
Validation Analyst 3-1
Rockford, IL · On-site
$27.27 - $30.68/hr
The Validation Analyst III is responsible for overall validation project management of large ... and cleaning validation protocols. * Reviews production jacket and issuance to ensure that ...
For Microbiological Cleaning Validation Specialist services in the Microbiological area WHAT MAKES ... Contribute microbiological expertise to root-cause analysis, product-impact assessment, risk ...
For Microbiological Cleaning Validation Specialist services in the Microbiological area WHAT MAKES ... Contribute microbiological expertise to root-cause analysis, product-impact assessment, risk ...
Validation Engineer
Raleigh, NC · On-site
The role requires strong technical writing, analytical thinking, and hands-on execution. Requirements: Key Responsibilities: * Execute and support cleaning validation activities, including protocol ...
Quick apply
Validation Engineer
Raleigh, NC · On-site
The role requires strong technical writing, analytical thinking, and hands-on execution. Requirements: Key Responsibilities: * Execute and support cleaning validation activities, including protocol ...
Validation Engineer IV
Rockville, MD · On-site
... analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the Validation Engineer must be ...
Quick apply
Validation Engineer IV
Rockville, MD · On-site
... analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the Validation Engineer must be ...
Validation Engineer II
Rockville, MD · On-site
... analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the Validation Engineer must be ...
Quick apply
Validation Engineer II
Rockville, MD · On-site
... analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the Validation Engineer must be ...
Validation Engineer II
Rockville, MD · On-site
... validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the ...
Validation Engineer II
Rockville, MD · On-site
... validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the ...
Validation Engineer II
Rockville, MD · On-site
... analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the Validation Engineer must be ...
Validation Engineer II
Rockville, MD · On-site
... analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the Validation Engineer must be ...
Validation Engineer IV
Rockville, MD · On-site
... validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the ...
Validation Engineer IV
Rockville, MD · On-site
... validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the ...
Validation Engineer II
Rockville, MD · On-site
... validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the ...
Validation Engineer II
Rockville, MD · On-site
... validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the ...
Validation Engineer I
Rockville, MD · On-site
... analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the validation specialist must be ...
Validation Engineer I
Rockville, MD · On-site
... analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the validation specialist must be ...
Cleaning Validation Analyst information
See salary details
$20.19 - $26.44
1% of jobs
$26.44 - $32.69
7% of jobs
$32.69 - $38.94
14% of jobs
$39.86 is the 25th percentile. Wages below this are outliers.
$38.94 - $45.19
18% of jobs
The median wage is $50.82 / hr.
$45.19 - $51.44
11% of jobs
$51.44 - $57.69
13% of jobs
$57.69 - $63.94
9% of jobs
$67.07 is the 75th percentile. Wages above this are outliers.
$63.94 - $70.19
5% of jobs
$70.19 - $76.44
3% of jobs
$76.44 - $82.69
7% of jobs
$82.69 - $88.94
12% of jobs
$20
$56
$88
How much do cleaning validation analyst jobs pay per hour?
As of Sep 14, 2026, the average hourly pay for cleaning validation analyst in the United States is $56.31, according to ZipRecruiter salary data. Most workers in this role earn between $40.87 and $75.00 per hour, depending on experience, location, and employer.
What are popular job titles related to Cleaning Validation Analyst jobs?
For Cleaning Validation Analyst jobs, the most frequently searched job titles are:
Staff Engineer - Process & Cleaning Validation
Zebulon, NC • On-site
PM Group
Contractor
Re-posted 10 days ago
Job description
Overview
The Staff Engineer - Process & Cleaning Validation position is an exciting opportunity to join PM Group's quickly growing Outsourced Technical Services(OTS) team near Zebulon, NC. Outsourced Technical Services (OTS) is an integral part of PM Group's ability to support clients across the complete project life cycle. We have over 50 years' industry experience, strong technical knowledge and integrated resources. Clients look to us to provide experienced technical professionals that complement their project teams. Together we are sharing knowledge, learning, growing and continuing to be an integral part of supporting PM Group's ongoing expansion in the US.
We are seeking an experienced Staff Engineer, Process & Cleaning Validation to support manufacturing operations by ensuring processes and cleaning procedures are validated, compliant, and capable of consistently delivering high-quality products in a regulated sterile/aseptic environment.
PM Group is an employee owned, international project delivery firm with a team of 4,000+ people. We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors. From our network of offices in Europe, Asia and the US, we work with the world's leading organizations. We are focused on growing a sustainable business centered on our people, our clients and trade partners.
Responsibilities
Qualifications
All of your information is confidential according to EEO guidelines.
Why PM Group?
As an employee-owned company, we are inclusive, committed and driven. Corporate Responsibility and Sustainability are the heart of our new 2026 business strategy. Click here to read more in our 2025 Environmental, Social and Governance Report.
Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future.
PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. If you require any assistance in this regard, please let us know.
RECRUITMENT AGENCIES NEED NOT APPLY
#LI-TF1
The Staff Engineer - Process & Cleaning Validation position is an exciting opportunity to join PM Group's quickly growing Outsourced Technical Services(OTS) team near Zebulon, NC. Outsourced Technical Services (OTS) is an integral part of PM Group's ability to support clients across the complete project life cycle. We have over 50 years' industry experience, strong technical knowledge and integrated resources. Clients look to us to provide experienced technical professionals that complement their project teams. Together we are sharing knowledge, learning, growing and continuing to be an integral part of supporting PM Group's ongoing expansion in the US.
We are seeking an experienced Staff Engineer, Process & Cleaning Validation to support manufacturing operations by ensuring processes and cleaning procedures are validated, compliant, and capable of consistently delivering high-quality products in a regulated sterile/aseptic environment.
PM Group is an employee owned, international project delivery firm with a team of 4,000+ people. We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors. From our network of offices in Europe, Asia and the US, we work with the world's leading organizations. We are focused on growing a sustainable business centered on our people, our clients and trade partners.
Responsibilities
- Lead process validation (PPQ) and cleaning validation activities.
- Develop validation strategies for new and existing products, processes, and equipment.
- Author, review, and execute validation protocols and reports.
- Analyze data and compile conclusions to support validation activities.
- Support change controls, deviation investigations, and CAPA initiatives.
- Collaborate with cross-functional teams including Manufacturing, Quality, and Technical Operations.
- Ensure compliance with cGMP requirements and regulatory expectations.
- Participate in internal and external audits and regulatory inspections.
- Drive continuous improvement initiatives related to validation programs.
Qualifications
- Bachelor's degree in Engineering, Chemistry, Life Sciences, or a related technical discipline.
- 8+ years of experience in process validation and/or cleaning validation within a regulated manufacturing environment.
- Hands-on experience in sterile or aseptic manufacturing environments is required.
- Strong knowledge of cleaning validation principles, including residue limits, risk assessments, and risk-based validation approaches.
- Experience with lifecycle process validation and Process Performance Qualification (PPQ).
- Strong understanding of cGMP regulations and industry standards.
- Excellent analytical, problem-solving, and data interpretation skills.
- Proven technical writing and documentation experience.
- Ability to manage multiple priorities and projects simultaneously.
- Strong communication and cross-functional collaboration abilities.
- Demonstrated attention to detail and commitment to quality and compliance.
All of your information is confidential according to EEO guidelines.
Why PM Group?
As an employee-owned company, we are inclusive, committed and driven. Corporate Responsibility and Sustainability are the heart of our new 2026 business strategy. Click here to read more in our 2025 Environmental, Social and Governance Report.
Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future.
PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. If you require any assistance in this regard, please let us know.
RECRUITMENT AGENCIES NEED NOT APPLY
#LI-TF1