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Process Validation Engineer Jobs in Pennsylvania

Cadence Inc

Validation Engineer II

Cranberry Township, PA · On-site

$83K - $105K/yr

Contribute to process improvements and continuous improvement initiatives. Qualifications: * Bachelor's in Engineering, Life Sciences, or related field. * 3+ years' experience in validation or ...

CAI

Validation Engineer

King Of Prussia, PA · On-site

$72K - $80K/yr

... processes, and elite expertise developed over 30 years. Our Purpose We exist to be the trusted ... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and ...

CAI

Validation Engineer

Philadelphia, PA · On-site

$72K - $80K/yr

... processes, and elite expertise developed over 30 years. Our Purpose We exist to be the trusted ... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and ...

CAI

Validation Engineer

Fogelsville, PA · On-site

$72K - $80K/yr

... processes, and elite expertise developed over 30 years. Our Purpose We exist to be the trusted ... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and ...

CAI

Validation Engineer

Harrisburg, PA

$72K - $80K/yr

... processes, and elite expertise developed over 30 years. Our Purpose We exist to be the trusted ... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and ...

CAI

Validation Engineer

Harrisburg, PA · On-site

$72K - $80K/yr

... processes, and elite expertise developed over 30 years. Our Purpose We exist to be the trusted ... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and ...

CAI

Validation Engineer

Philadelphia, PA

$72K - $80K/yr

... processes, and elite expertise developed over 30 years. Our Purpose We exist to be the trusted ... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and ...

CAI

Validation Engineer

Philadelphia, PA

$72K - $80K/yr

... processes, and elite expertise developed over 30 years. Our Purpose We exist to be the trusted ... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and ...

CAI

Validation Engineer

Harrisburg, PA

$72K - $80K/yr

... processes, and elite expertise developed over 30 years. Our Purpose We exist to be the trusted ... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and ...

CAI

Validation Engineer

Allentown, PA · On-site

$72K - $80K/yr

... processes, and elite expertise developed over 30 years. Our Purpose We exist to be the trusted ... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and ...

CAI

Validation Engineer

King Of Prussia, PA · On-site

$72K - $80K/yr

... processes, and elite expertise developed over 30 years. Our Purpose We exist to be the trusted ... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and ...

CAI

Validation Engineer

King Of Prussia, PA

$72K - $80K/yr

... processes, and elite expertise developed over 30 years. Our Purpose We exist to be the trusted ... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and ...

CAI

Validation Engineer

King Of Prussia, PA

$72K - $80K/yr

... processes, and elite expertise developed over 30 years. Our Purpose We exist to be the trusted ... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and ...

CAI

Validation Engineer

Marietta, PA · On-site

$72K - $80K/yr

... processes, and elite expertise developed over 30 years. Our Purpose We exist to be the trusted ... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and ...

CAI

Validation Engineer

Harrisburg, PA · On-site

$72K - $80K/yr

... processes, and elite expertise developed over 30 years. Our Purpose We exist to be the trusted ... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and ...

CAI

Validation Engineer

Allentown, PA · On-site

$72K - $80K/yr

... processes, and elite expertise developed over 30 years. Our Purpose We exist to be the trusted ... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and ...

CAI

Validation Engineer

Marietta, PA · On-site

$60 - $80/hr

... processes, and elite expertise developed over 30 years. Our Purpose We exist to be the trusted ... a science or engineering field (or equivalent experience) * - 2-4 years' experience in ...

CAI

Validation Engineer

Marietta, PA · On-site

$72K - $80K/yr

... processes, and elite expertise developed over 30 years. Our Purpose We exist to be the trusted ... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and ...

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Process Validation Engineer information

See Pennsylvania salary details

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How much do process validation engineer jobs pay per hour?

As of Sep 8, 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 Project Manager

LAPORTE L.C.C.

Philadelphia, PA • On-site

Full-time

PTO

Re-posted 7 days ago

Key responsibilities

  • Plan, coordinate, and execute facility improvement projects, including scope definition, scheduling, contractor coordination, and closeout documentation.

  • Serve as the primary on-site liaison for all project-related activities, ensuring minimal disruption to GMP operations and maintaining a safe working environment throughout project execution.

  • Initiate, author, and shepherd change control records through the site quality management system (QMS) in accordance with GMP change control procedures.

Job description

Process & Validation Project Manager (a minimum of 5 years of experience required)
Location: Philadelphia, PA
Employment Type: Full-time, mostly onsite
About Us
Are you ready to take the next step in your career? LAPORTE, a consulting engineering firm with 25 years of experience and a strong presence in North America and Europe, is seeking an Process & Validation Project Manager to join our growing team. With 25 offices and over 480 employees worldwide, we specialize in delivering innovative solutions for the pharmaceutical and food & beverage industries.
As we continue to expand our presence in the Greater Philadelphia life sciences market, we are seeking an experienced Process & Validation Project Manager to lead capital projects, facility improvements, commissioning and qualification initiatives, and GMP manufacturing enhancements for our pharmaceutical and biotechnology clients.
This role offers the opportunity to work directly with industry-leading organizations while contributing to technically challenging projects that improve manufacturing performance, quality, and compliance.
At LAPORTE, we offer:
  • Competitive Salary
  • Comprehensive Benefits
  • Compensatory Paid Time Off (PTO)
  • Paid Parental Leave
  • A Flexible Work Environment that values work-life balance
  • Opportunities for Professional Growth

Responsibilities and Duties:
  • Plan, coordinate, and execute facility improvement projects, including scope definition, scheduling, contractor coordination, and closeout documentation.
  • Serve as the primary on-site liaison for all project-related activities, ensuring minimal disruption to GMP operations and maintaining a safe working environment throughout project execution.
  • Initiate, author, and shepherd change control records through the site quality management system (QMS) in accordance with GMP change control procedures.
  • Coordinate and support the vendor approval and qualification process for new contractors and service providers, partnering with Procurement and QA as required.
  • Develop and maintain project schedules, status trackers, and progress reports for review by site leadership.
  • Identify and escalate project risks, scope changes, and schedule impacts in a timely manner, proposing mitigation strategies as appropriate.
  • Ensure all project activities comply with applicable GMP regulations, site SOPs, EHS requirements, and local building codes.

Qualifications:
  • Bachelor's degree in Engineering, Life Sciences, Construction Management, Project Management, or a related technical field.
  • Minimum of 5 years of project management experience supporting pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.
  • Demonstrated success managing engineering, facility, equipment installation, capital improvement, or operational excellence projects from initiation through closeout.
  • Experience developing and maintaining project schedules, coordinating resources, tracking milestones, and driving projects to successful completion.
  • Strong experience managing contractors, vendors, and cross-functional teams in a GMP-regulated environment.
  • Proven ability to lead project meetings, communicate project status, and effectively manage stakeholder expectations at all organizational levels.
  • Working knowledge of cGMP regulations and quality systems, including change management processes.
  • Exceptional organizational, communication, problem-solving, and relationship management skills.
  • Ability to manage multiple priorities and adapt to changing project requirements in a fast-paced environment.
  • Willingness to travel to client sites as required.

Preferred Qualifications
  • Experience overseeing facility renovations, equipment installations, utility upgrades, or manufacturing process improvement projects.
  • Familiarity with project budgeting, forecasting, cost tracking, and resource planning.
  • Experience coordinating activities across Engineering, Manufacturing, Quality Assurance, Validation, Maintenance, and Procurement teams.
  • PMP certification or similar project management credential.
  • Knowledge of commissioning, qualification, and validation processes within life sciences manufacturing environments.
  • Experience working in aseptic processing, biotechnology, cell and gene therapy, or sterile manufacturing facilities.
  • Familiarity with risk management methodologies and structured problem-solving tools.

Send us your application today. We look forward to meeting you!
The LAPORTE team

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