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Process Validation Engineer Jobs in Pennsylvania

Peregrine Team

Validation Engineer

Philadelphia, PA · On-site

Peregrine Team is hiring a Validation Engineer to support equipment and process validation within a regulated pharmaceutical environment. This role ensures compliance with regulatory standards and ...

Onsite Personnel LLC

Validation Engineer

Newtown, PA · On-site

Validation Engineer: Support site commissioning and qualification, which includes but is not limited to the following: equipment, utilities, cleaning, process, assay qualifications. Ensuring the ...

Xyntek Inc.

Validation Engineer

Montgomeryville, PA · On-site

$80 - $100/hr

Work on a variety of programmable logic controller systems and a variety of Distributed Controls ... Design, program,test, validate, and maintain process controls and automation systems ...

Catalyx

Validation Engineer

Horsham, PA · On-site

Catalyx Services, LLC seeks a Validation Engineer reporting to office in Montgomeryville, PA to ... Design, program, test, validate, and maintain process controls and automation systems, including ...

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How much do process validation engineer jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for process validation engineer in Pennsylvania is $39.63, according to ZipRecruiter salary data. Most workers in this role earn between $23.12 and $51.59 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 Pennsylvania?

For Process Validation Engineer jobs in Pennsylvania, the most frequently searched job titles are:

What job categories do people searching Process Validation Engineer jobs in Pennsylvania look for?

The top searched job categories for Process Validation Engineer jobs in Pennsylvania are:

What are popular job titles related to Process Validation Engineer jobs in PA?

For Process Validation Engineer jobs in PA, the most frequently searched job titles are:

Process Validation Engineer jobs near you
Infographic showing various Process Validation Engineer job openings in Pennsylvania as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, 2% Contract, and 1% Nights. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $82,434 per year, or $39.6 per hour.

Process Validation Engineer - TMV

2T Consulting

Spring Creek, PA • On-site

Full-time

Posted 19 days ago

Job description

We are seeking a Process Validation Engineer with hands-on experience in Test Method Validation (TMV) within a regulated manufacturing environment. The role will be responsible for leading TMV remediation activities, executing validation protocols, analyzing results, and ensuring validation activities are completed in accordance with quality-system requirements.

Key Responsibilities
  • Lead and execute Test Method Validation (TMV) and remediation activities.
  • Develop, review, execute, and support the approval of TMV protocols and final validation reports.
  • Plan and perform validation testing, including sample preparation, test method execution, and data collection.
  • Analyze validation results and document findings, deviations, and issues identified during execution.
  • Apply statistical methods, including Gage R&R, to assess test method capability and support validation conclusions.
  • Troubleshoot validation issues and collaborate with relevant teams to identify and implement effective resolutions.
  • Support operator training to ensure consistent and compliant execution of validated test methods.
  • Partner cross-functionally with Engineering, Quality, Manufacturing, and other stakeholders to complete validation activities.
  • Maintain accurate validation records and documentation in accordance with quality-system and regulatory requirements.
  • Track TMV remediation activities and timelines and drive assigned activities through successful completion.
  • Support continuous improvement of manufacturing and validation processes as needed.
Required Qualifications & Experience
  • Hands-on experience with Test Method Validation (TMV) activities.
  • Experience with the complete validation lifecycle, including protocol development, execution, data analysis, and final reporting.
  • Strong knowledge of statistical analysis, including Gage R&R and measurement system analysis (MSA).
  • Experience working in a regulated manufacturing environment, preferably within the medical device industry.
  • Strong technical writing, documentation, and validation report-writing skills.
  • Ability to independently plan and execute validation activities while meeting established timelines.
  • Experience working collaboratively with Engineering, Quality, Manufacturing, and Operations teams.
  • Strong analytical, organizational, problem-solving, and communication skills.

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