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

The Senior Engineer, Process Validation is responsible for leading & supporting internal and external validation projects that enable commercialization of vital new life saving medicines. This ...

This role manages equipment qualification, process validation, computer system validation, and ... Partners with Manufacturing, Engineering, Quality, Regulatory Affairs, Research and Development ...

The Validation Engineer in this role will be trained to support validation projects of medium complexity (equipment, utilities, facilities, processes, computerized systems, etc.) in areas such as ...

Contribute to the continuous improvement of validation processes and procedures. What we are looking for: * Bachelor's degree in Engineering (Chemical, Biomedical, Mechanical, or equivalent) or a ...

Client- Haliburton FPGA Design & Validation Engineer (Oil & Gas Systems) Houston, TX, USA Long term ... You will leverage VHDL to implement complex data acquisition and signal processing algorithms that ...

Contribute to the continuous improvement of validation processes and procedures. What we are looking for: * Bachelor's degree in Engineering (Chemical, Biomedical, Mechanical, or equivalent) or a ...

... processes, and elite expertise developed over 30 years. Our approach is simple because our Purpose ... Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ...

... processes, and elite expertise developed over 30 years. Our approach is simple because our Purpose ... Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ...

Senior Process Engineer

Stafford, TX · On-site

$90K - $117K/yr

The Senior Process Engineer is a key individual contributor responsible for the development, optimization, validation, and sustainment of manufacturing processes supporting medical device products.

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Process Validation Engineer information

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$66

How much do process validation engineer jobs pay per hour?

As of Jul 6, 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 are Process Validation Engineers?

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 are the key skills and qualifications needed to thrive as a Process Validation Engineer, and why are they important?

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:
Senior Engineer, Process Validation

Senior Engineer, Process Validation

Danaher

Houston, TX • On-site, Remote

$100K - $130K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 17 days ago


Danaher rating

7.5

Company rating: 7.5 out of 10

Based on 28 frontline employees who took The Breakroom Quiz


Job description

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.

You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.

At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you'll help bring life-changing innovations to life-impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential-one discovery at a time.

Learn about the Danaher Business System which makes everything possible.

The Senior Engineer, Process Validation is responsible for leading & supporting internal and external validation projects that enable commercialization of vital new life saving medicines.

This position reports to the Process Validation Manager and is part of the Technical Operations Department located in Fargo, ND and will be fully remote.

In this role, you will have the opportunity to:

  • Design, execute, and summarize deliverables across the three stages of process validation supporting process characterization and qualification spanning critical starting materials, drug substance, and drug product, product classifications aligned with FDA guidance, EU GMP Annex 15, and lifecycle approach.
  • Lead the planning, execution, and lifecycle management of sterile fill-finish process validation strategies and qualification programs for aseptic manufacturing processes including sterile filtration, aseptic process simulation, sterile filling, visual inspection, container closure integrity testing, filter validation, labelling, packaging and shipping.
  • Drive risk-based approaches using tools such as pFMEA, risk ranking, and criticality assessments and apply statistical tools to evaluate process performance, including but not limited to process capability, trend analysis and control charts and DOE) interpretation.
  • Serve as a technical SME for process validation with external clients, across internal teams such as MSAT, manufacturing, QC, QA and RA, and during client audits and regulatory inspections, kaizens and workshop events.
  • Mentor junior validation associates in Process Validation, cGMP regulations, and principles of Quality by Design

The essential requirements of the job include:

  • Bachelor or master degree in engineering and 5+ years of experience
  • Prior experience in leading process development, engineering, and deliverables across all three stages of process validation in biologics/small and large molecules manufacturing train using statistical analysis, risk assessment, and process improvement tools required.
  • Knowledge of global regulatory requirements and cGMP regulations for pharmaceutical manufacturing operations and validation procedures and practices.
  • Proficiency in technical writing with deviation investigations, root cause analysis, and risk assessments.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

  • Ability to travel 15% to site to support validation project executions, routine inspections, audits, and client visits.

It would be a plus if you also possess previous experience in:

  • Packaging and shipping validation of final product container closure configurations.
  • Client facing roles such as prior experience in a CDMO environment

Aldevron, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

At Aldevron we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Aldevron can provide.

The annual salary range for this role is $100,000 to $130,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.

This job is also eligible for bonus/incentive pay.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.

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Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.


For more information, visit www.danaher.com.


Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.


The U.S. EEO posters are available here.


For candidates who are based outside of New York City or who are applying for roles outside of New York City, for more information about conditions of any job offer please click here.


We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistance@danaher.com.


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About Danaher

Sourced by ZipRecruiter

We are a science and technology innovator committed to helping our customers solve complex challenges, and improving quality of life around the world. A global family of more than 20 operating companies, we drive meaningful innovation in some of today's most dynamic, growing industries.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Washington, DC, US

Year founded

1984