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Process Validation Engineer Jobs in Houston, TX (NOW HIRING)

LGM Pharma, LLC

MANUFACTURING ENGINEER

Rosenberg, TX · On-site

$80K - $100K/yr

Support new product introductions, process scale-up, technology transfers and process validation activities. * Support customer, regulatory, and internal audits. Process Engineering & Continuous ...

ON.energy

Manufacturing Engineer

Houston, TX

$69K - $89K/yr

Support new product introduction, pilot builds, process validation, and ramp-up activities. Partner with design engineering to improve manufacturability, assembly methods, and process robustness.

Deloitte

System Test and Validation Lead

Houston, TX · On-site +1

Bachelor's degree in business, information systems, computer science, engineering, or equivalent ... Experience with AI governance processes, including AI use case tracking, model risk classification ...

Deloitte

System Test and Validation Lead

Houston, TX · On-site +1

Bachelor's degree in business, information systems, computer science, engineering, or equivalent ... Experience with AI governance processes, including AI use case tracking, model risk classification ...

Deloitte

System Test and Validation Lead

Houston, TX · On-site +1

Bachelor's degree in business, information systems, computer science, engineering, or equivalent ... Experience with AI governance processes, including AI use case tracking, model risk classification ...

ON.energy

Manufacturing Engineer

Houston, TX · On-site

$69K - $89K/yr

... process validation, and ramp-up activities. • Partner with design engineering to improve manufacturability, assembly methods, and process robustness. • Monitor process capability, yield, cycle ...

Workover Solutions

Mechanical Engineer

Houston, TX · On-site

Support product and process validation activities in accordance with established standards, procedures, and quality expectations. * Collaborate with engineering, quality, manufacturing, and ...

CSAT Solutions

Process Engineer

Houston, TX · On-site

Develop, implement, validate, and continuously improve repair processes to maximize throughput ... Support engineering technicians and repair operations with technical troubleshooting, process ...

CSAT Solutions

Process Engineer

Houston, TX

Develop, implement, validate, and continuously improve repair processes to maximize throughput ... Support engineering technicians and repair operations with technical troubleshooting, process ...

New

CSAT Solutions

Process Engineer

Houston, TX

Develop, implement, validate, and continuously improve repair processes to maximize throughput ... Support engineering technicians and repair operations with technical troubleshooting, process ...

New

DPS Group

Process Engineer

Houston, TX · On-site

Arcadis is seeking a Process Engineer that will be responsible for evaluating current processes and ... HACCP and cGMP (Change control, CAPA, Deviation, Audit, Validation) * Process control & continuous ...

Bayport Laboratories LLC

Process Engineer

Houston, TX · On-site

... validation of new manufacturing processes, equipment, and technologies. 4. Perform process ... Bachelor's degree in Chemical Engineering or related field. Required Knowledge: * Understanding of ...

Envirogen

Process Engineer

Kingwood, TX · On-site

... interpret complex data matrices to validate cutting-edge designs and accelerate the ... Process engineering), backed by a strong foundation water systems. * Proven Track Record:

Salas O'Brien, Inc.

Process Engineer

Houston, TX

... validation activities, and change control processes. * Communication: * Communicate effectively with clients, contractors, and project teams regarding technical scope, deliverables, and compliance ...

Envirogen

Process Engineer

Kingwood, TX · On-site

... interpret complex data matrices to validate cutting-edge designs and accelerate the ... Process engineering), backed by a strong foundation water systems. * Proven Track Record:

Topbuild

Process Engineer

Houston, TX

$75K - $150K/yr

Our Process Engineers work closely with the fabrication, pricing, and sales teams to develop ... If operating a Company Vehicle, a valid driver's license will be required. * 5 years of ...

TopBuild Corp.

Process Engineer

Houston, TX · On-site

$75K - $150K/yr

Our Process Engineers work closely with the fabrication, pricing, and sales teams to develop ... If operating a Company Vehicle, a valid driver's license will be required. * 5 years of ...

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Process Validation Engineer information

See Houston, TX salary details

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How much do process validation engineer jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for process validation engineer in Houston, TX is $37.76, according to ZipRecruiter salary data. Most workers in this role earn between $22.02 and $49.13 per hour, depending on experience, location, and employer.

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 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 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.

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 safe, effective, and compliant with industry regulations.

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 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 popular job titles related to Process Validation Engineer jobs in Houston, TX?

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

What job categories do people searching Process Validation Engineer jobs in Houston, TX look for?

The top searched job categories for Process Validation Engineer jobs in Houston, TX are:

Process Validation Engineer jobs near you
Infographic showing various Process Validation Engineer job openings in Houston, TX as of August 2026, with employment types broken down into 74% Full Time, and 26% Contract. Highlights an 100% In-person job distribution, with an average salary of $78,534 per year, or $37.8 per hour.

MANUFACTURING ENGINEER

LGM Pharma, LLC

Rosenberg, TX • On-site

$80K - $100K/yr

Full-time

Medical, Dental, Vision, Retirement

Posted 24 days ago

Job description

Manufacturing & Equipment Support

  • Provide technical leadership in Troubleshooting manufacturing and packaging equipment to minimize downtime and improve equipment reliability.
  • Analyze manufacturing performance data to increase throughput, labor efficiency, and Overall Equipment Effectiveness (OEE).
  • Lead Root Cause Analysis (RCA) investigations for manufacturing issues and implement sustainable corrective actions.
  • Lead installation, commissioning, startup, and qualification of new manufacturing and packaging equipment.
  • Develop and review User Requirement Specifications (URS), and support Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT).
  • Maintain equipment lifecycle documentation and ensure equipment remains qualified and production ready.
  • Support new product introductions, process scale-up, technology transfers and process validation activities.
  • Support customer, regulatory, and internal audits.

Process Engineering & Continuous Improvement

  • Develop, optimize, and standardize manufacturing processes. Analyze manufacturing trends and KPI’s to identify opportunities for process optimization and cost reduction.
  • Conduct engineering studies to improve capacity, cycle times, manufacturing flow, and reduce waste.
  • Monitor manufacturing KPIs and identify opportunities to improve efficiency and reduce costs.
  • Lead Lean Manufacturing, Kaizen, Six Sigma, and 5S initiatives.
  • Develop and revise manufacturing work instructions and SOPs.

Quality & Validation

  • Support equipment qualification and process and cleaning validation activities, including IQ/OQ/PQ.
  • Prepare and review qualification protocols and reports.
  • Participate in deviation investigations, root cause analysis, CAPA implementation, and change control activities.
  • Support execution of Validation Master Plan activities and remediation of legacy equipment documentation.
  • Ensure engineering documentation complies with FDA and current Good Manufacturing Practice (cGMP) requirements.

Qualifications

  • Bachelor's degree in Mechanical, Chemical, Industrial, Manufacturing, Electrical Engineering, or a related engineering discipline.
  • Five (5) or more years of engineering experience in pharmaceutical manufacturing or another regulated industry.
  • Working knowledge of FDA regulations and current Good Manufacturing Practices (cGMP).
  • Experience with equipment qualification, process validation, and cleaning validation.
  • Experience with pharmaceutical liquids, semi-solids, and/or packaging operations.
  • Knowledge of Lean Manufacturing, Six Sigma, and 5S methodologies.
  • Experience with technology transfers, change control, deviation investigations, and CAPA.
  • Experience using SAP or another ERP system.
  • Strong analytical, problem-solving, root cause analysis, technical writing, and communication skills.
  • Demonstrated ability to lead cross-functional teams and manage multiple priorities.



At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer. We offer medical, dental, vision and company matching 401K.

All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.