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Process Validation Engineer Jobs in Rocky Mount, NC

Actalent

Validation Engineer

Wilson, NC · On-site

$47 - $52/hr

Experience with validation protocols and process validation. * Knowledge of Installation ... Engineering background with a focus on validation. Work Environment The work environment involves ...

Pinnaql

Validation Engineer

Wilson, NC · On-site

Process systems and supporting utilities * Equipment and system turnover documentation * IQ/OQ/PQ execution Required Qualifications * Bachelor's degree in Engineering, Science, or a related technical ...

Pinnaql

Validation Engineer

Wilson, NC · On-site

Process systems and supporting utilities * Equipment and system turnover documentation * IQ/OQ/PQ execution Required Qualifications * Bachelor's degree in Engineering, Science, or a related technical ...

Pinnaql

Validation Engineer

Wilson, NC · On-site

Process systems and supporting utilities * Equipment and system turnover documentation * IQ/OQ/PQ execution Required Qualifications * Bachelor's degree in Engineering, Science, or a related technical ...

Pinnaql

Validation Engineer

Wilson, NC · On-site

Process systems and supporting utilities * Equipment and system turnover documentation * IQ/OQ/PQ execution Required Qualifications * Bachelor's degree in Engineering, Science, or a related technical ...

Pinnaql, Inc.

Validation Engineer

Wilson, NC · On-site

$85 - $130/hr

Process systems and supporting utilities * Equipment and system turnover documentation * IQ/OQ/PQ execution Required Qualifications * Bachelor's degree in Engineering, Science, or a related technical ...

Pinnaql

Validation Engineer

Wilson, NC · On-site

Process systems and supporting utilities * Equipment and system turnover documentation * IQ/OQ/PQ execution Required Qualifications * Bachelor's degree in Engineering, Science, or a related technical ...

Pinnaql

Validation Engineer

Wilson, NC · On-site

Process systems and supporting utilities * Equipment and system turnover documentation * IQ/OQ/PQ execution Required Qualifications * Bachelor's degree in Engineering, Science, or a related technical ...

Pinnaql

Validation Engineer

Wilson, NC · On-site

Process systems and supporting utilities * Equipment and system turnover documentation * IQ/OQ/PQ execution Required Qualifications * Bachelor's degree in Engineering, Science, or a related technical ...

Pinnaql

Validation Engineer

Wilson, NC · On-site

$85 - $120/hr

Process systems and supporting utilities * Equipment and system turnover documentation * IQ/OQ/PQ execution Required Qualifications * Bachelor's degree in Engineering, Science, or a related technical ...

Pinnaql

Validation Engineer

Wilson, NC

Process systems and supporting utilities * Equipment and system turnover documentation * IQ/OQ/PQ execution Required Qualifications * Bachelor's degree in Engineering, Science, or a related technical ...

Pinnaql

Validation Engineer

Wilson, NC · On-site

Process systems and supporting utilities * Equipment and system turnover documentation * IQ/OQ/PQ execution Required Qualifications * Bachelor's degree in Engineering, Science, or a related technical ...

Pharma Bioserv

Be Seen First

Process Engineer

Wilson, NC · On-site

Supporting New Product Introduction/ process validation in Downstream manufacturing facility ... engineering companies within the regulated industry for more than 30 years. Since our inception ...

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All JobsProcess Validation Engineer JobsProcess Validation Engineer Jobs in Rocky Mount, NC

Process Validation Engineer information

See Rocky Mount, NC salary details

$7

$38

$66

How much do process validation engineer jobs pay per hour?

As of Aug 31, 2026, the average hourly pay for process validation engineer in Rocky Mount, NC is $38.10, according to ZipRecruiter salary data. Most workers in this role earn between $22.26 and $49.57 per hour, depending on experience, location, and employer.

What is a process validation engineer?

Process Validation Engineers are professionals responsible for ensuring that manufacturing processes consistently produce products that meet predetermined quality standards. They design, execute, and document validation protocols to verify that equipment, systems, and processes operate effectively and efficiently. These engineers play a crucial role in regulated industries such as pharmaceuticals, biotechnology, and medical devices, where compliance with industry standards and regulatory requirements is essential. Their work helps to minimize risks, ensure product safety, and maintain regulatory compliance.

What are the key skills and qualifications needed to thrive as a process validation engineer?

To thrive as a Process Validation Engineer, you need a solid background in engineering or life sciences, a thorough understanding of validation protocols, and knowledge of industry regulations such as GMP. Experience with validation software, statistical analysis tools, and familiarity with regulatory documentation systems are typically required. Strong analytical thinking, attention to detail, and effective communication skills help you resolve issues and coordinate cross-functional teams. These skills and qualities are essential to ensure processes are compliant, efficient, and produce high-quality, safe products.

What are some common challenges faced by process validation engineers during product scale-up?

Process Validation Engineers often encounter challenges when scaling up products from development to full-scale manufacturing. These can include ensuring process consistency, managing variations in equipment or raw materials, and troubleshooting unexpected deviations that may not have surfaced during small-scale trials. Effective communication with cross-functional teams—such as quality assurance, production, and R&D—is essential to quickly address issues and maintain compliance with regulatory requirements. Being proactive and detail-oriented helps navigate these complexities and ensures successful validation outcomes.

What is the difference between Process Validation Engineer vs Quality Assurance Engineer?

AspectProcess Validation EngineerQuality Assurance Engineer
Primary FocusValidating manufacturing processes to ensure product quality and complianceDeveloping and implementing quality systems and procedures to prevent defects
CertificationsGMP, ISO, Six Sigma often preferredISO, Six Sigma, CQE certifications common
Work EnvironmentManufacturing, pharmaceutical, biotech facilitiesQuality departments across various industries
Key ResponsibilitiesProcess validation, protocol development, troubleshootingAudits, quality audits, process improvements

While both roles aim to ensure product quality, the Process Validation Engineer primarily focuses on validating manufacturing processes, whereas the Quality Assurance Engineer oversees overall quality systems and compliance. Both roles often collaborate but serve distinct functions within the quality management framework.

Do process validation engineers make good money?

Process validation engineers typically earn competitive salaries that vary by industry, experience, and location. They often have specialized skills in quality assurance, regulatory compliance, and validation tools, which can lead to higher compensation levels. Overall, the role is considered well-paying within manufacturing, pharmaceutical, and biotech sectors.

What does a process validation engineer do?

A process validation engineer is responsible for developing, executing, and documenting validation protocols to ensure manufacturing processes meet quality and regulatory standards. They analyze process data, identify risks, and implement improvements using tools like statistical analysis and validation software. Their work helps ensure products are consistently produced to specifications and comply with industry regulations.

What are popular job titles related to Process Validation Engineer jobs in Rocky Mount, NC?

For Process Validation Engineer jobs in Rocky Mount, NC, the most frequently searched job titles are:

What job categories do people searching Process Validation Engineer jobs in Rocky Mount, NC look for?

The top searched job categories for Process Validation Engineer jobs in Rocky Mount, NC are:

Process Validation Engineer jobs near you
Infographic showing various Process Validation Engineer job openings in Rocky Mount, NC as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 18% Part Time, 4% Contract, and 1% Nights. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $79,248 per year, or $38.1 per hour.

Staff Engineer - Process & Cleaning Validation

PM Group

Zebulon, NC • On-site

Contractor

Re-posted 25 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
  • 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

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

Education:UNAVAILABLEEmployment Type: CONTRACTOR

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