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Validation Engineer Jobs in Allen, TX (NOW HIRING)

Mativ

Validation Engineer

Dallas, TX · On-site

Validation Engineer Mativ is a global leader in specialty materials headquartered in Alpharetta, Georgia. The Company offers a wide range of critical components and engineered solutions that connect ...

Texas Instruments

Validation Engineer

Dallas, TX · On-site

$75 - $95/hr

Love your job. The Product/Test Engineers at Texas Instruments are powered by a passion for ... team on validation, while also tackling challenging problems in achieving analog performance ...

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How much do validation engineer jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for validation engineer in Allen, TX is $48.37, according to ZipRecruiter salary data. Most workers in this role earn between $36.68 and $58.80 per hour, depending on experience, location, and employer.

What is a validation engineer?

A validation engineer is responsible for testing equipment and electrical systems used in the manufacturing process. As a validation engineer, your primary duty is to work with the other members of the validation team to ensure that these systems measure up to company and industry standards. Skills needed for a validation engineer job include the ability to accurately test, measure, and calibrate manufacturing equipment for maximum efficiency and quality.

What are the key skills and qualifications needed to thrive as a validation engineer, and why are they important?

To thrive as a Validation Engineer, you need a solid background in engineering, quality assurance, and regulatory compliance, typically backed by a degree in engineering or a related field. Familiarity with validation protocols, statistical analysis tools, and industry-specific regulations such as FDA, GMP, or ISO standards is essential. Strong analytical thinking, attention to detail, and effective communication set top performers apart in this role. These skills ensure that products and processes meet stringent quality and safety standards, minimizing risks and ensuring regulatory approval.

What are some common challenges validation engineers face when working cross-functionally with other departments?

Validation Engineers frequently collaborate with teams such as manufacturing, quality assurance, and research & development. One common challenge is aligning differing priorities and timelines between departments, which can sometimes delay validation projects. Effective communication skills and flexibility are crucial to navigating these cross-functional interactions, ensuring that all regulatory and quality requirements are met without hindering production schedules. Building strong working relationships and proactively addressing potential concerns can help Validation Engineers facilitate smoother project execution.

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

AspectValidation EngineerQuality Assurance Engineer
CertificationsGMP, ISO, Six SigmaISO, Six Sigma, CQA
Work EnvironmentRegulated industries like pharma, biotech, medical devicesManufacturing, software, and product development
Primary FocusEnsuring products meet specifications through validation processesPreventing defects through process and system improvements
Common UsageRegulatory compliance, validation protocolsProcess audits, quality systems

Validation Engineers focus on verifying that products and processes meet regulatory standards through validation protocols, especially in regulated industries. Quality Assurance Engineers concentrate on maintaining overall product quality by implementing and auditing quality systems. While both roles aim to ensure product safety and efficacy, Validation Engineers are more involved in validation activities, whereas QA Engineers focus on process improvement and defect prevention.

Is validation engineer a good job?

Validation engineers are responsible for ensuring that products and processes meet quality standards through testing and documentation, often in regulated industries like pharmaceuticals or manufacturing. The role typically requires attention to detail, knowledge of validation protocols, and familiarity with tools like GxP or FDA regulations. It can offer stable employment and opportunities for specialization and advancement.

What degree do you need to be a validation engineer?

Validation engineers typically hold a bachelor's degree in engineering, life sciences, or a related field. Some roles may require a master's degree or specialized certifications in quality assurance or validation processes. Strong knowledge of industry standards and experience with validation tools are also important.
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What cities near Allen, TX are hiring for Validation Engineer jobs?

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Validation Engineer jobs near you
Infographic showing various Validation Engineer job openings in Allen, TX as of August 2026, with employment types broken down into 100% Full Time. Highlights an 91% In-person, and 9% Remote job distribution, with an average salary of $100,601 per year, or $48.4 per hour.

Validation Engineer

Dallas, TX • On-site

Mativ
5 - 10K employees

6.6

Company rating: 6.6 out of 10

Based on 21 frontline employees who took The Breakroom Quiz

People enjoy working here

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Respectful managers

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Full-time

Posted 7 days ago

Job description

Validation Engineer
Mativ is a global leader in specialty materials headquartered in Alpharetta, Georgia. The Company offers a wide range of critical components and engineered solutions that connect, protect, and purify our world.
Mativ is a global leader in specialty materials headquartered in Alpharetta, Georgia. The Company offers a wide range of critical components and engineered solutions to solve our customers' most complex challenges.
Position Title: Validation Engineer
FLSA: Salary Exempt
Location: Dallas, Texas
Description:
The Validation Engineer is responsible for managing, inspecting, testing, and modifying the instrumentation, equipment, mechanics, and procedures used to manufacture products in accordance with all company Standard Operating Procedures and manufacturing instructions, and to ensure all systems and processes are running correctly and efficiently to produce high quality products. He/she will also be responsible for generating and executing the site validation master plan. This position has no direct reports.
responsibilities:
Performs validation studies on manufacturing equipment, including equipment set up and qualification, manufacturing process validation, as well as cleaning validation, and ensuring systems remain in a qualified, operational state of compliance associated with cGMP manufacturing work environment.
  • Generates, reviews, and executes the master validation plan, validation protocols (IQ, OQ, PQ) on equipment, utilities, and computerized systems ensuring compliance with cGMP.
  • Prepares all implementation of change request using the "Change Management Request" (CMR) process initiated internally or from customers by collecting all relevant documentation, initiating a change request, route for approvals, implement the plan and close the request accordingly.
  • Apply concepts of Continuous Monitoring through Statistical Process Control (SPC) to ensure the processes that have been transferred into production are monitored and controlled appropriately to maintain the equipment in a validated state.
  • Prepares protocols, reports, and other necessary documentation for validation to determine whether systems and processes meet required criteria and specifications; identifies root causes of production or equipment problems
  • Evaluating current equipment and procedures used in production to certify operations are within regulations
  • Investigates and conducts troubleshooting and root cause analysis of validation related incidents and deviations
  • Resolve CAPA's, non-conformances, protocol incidents, and change controls related to validation protocols
  • Generate data and reports for the validation periodic monitoring and re-qualification programs
  • Establish validation standards, develop testing protocols, prepare equipment, document test results and analyze results to ultimately determine if a new process or new equipment meets policies and standards.
  • Communicate with outside vendors to identify new equipment or perform equipment troubleshooting if problems arise.
  • Maintains validation documentation through the validation lifecycle including protocols, , deviations and corrective actions.
  • Perform risk assessments, failure mode effects analysis (FMEA), and statistical data analysis to support validation activities.
  • Represents the engineering process during customer, certification and regulatory audits (internal and external)
  • Assist in investigating deviations related to facilities, utilities, and equipment.
  • Participates in multi-functional department teams for facilities, utilities, and equipment to meet established project timelines; says current with regulatory trends and validation best practices to enhance validation strategies.
  • Write new and revise current Standard Operating Procedures (SOPs) and Work Instructions as needed.
  • Other duties as assigned by management.

qualifications:
Required
  • BS in Engineering (Chemical preferred), life sciences or related field.
  • 3+ years of validation work experience in a pharmaceutical and/or medical device industry.
  • Certified Quality Engineer/Validation professional a plus
  • Experience with validation of cleaning, software, automated systems, packaging and laboratory equipment desired.
  • Experience authoring and executing Validation protocols such as Installation and equipment operation.
  • Strong understanding of FDA regulations, cGMP, ISO 13485, ICH guidelines and risk management principles.
  • Proficiency in validation software, statistical analysis tools, and data integrity principles is a plus.
  • Strong problem-solving skills with the ability to analyze technical issues and propose solutions.
  • Excellent interpersonal, communication and documentation skills.
  • Ability to work independently and in cross-functional teams in a fast-paced environment.

Preferred
  • Must have the ability to work both independently and as a greater team. Must be able to coordinate work with customers, supervisors, and information partners frequently in different states and/or countries.
  • Must be able to work in a fast-paced environment. Must be able to manage multiple projects while minding priorities. Must be able to make informed, strategic decisions, even when under pressure or when working with resource limitations.
  • Must always have a mindset to protect the interests and health of our consumers, our company, and our customers.
  • Must work well cross-functionally, with partners from commercial, sales, supply chain, marketing, operations, etc.
  • Ability to work with limited supervision and take ownership of projects to meet scheduled timeline and technical goals; maintains accurate and thorough records
  • Experience writing SOPs and technical writing.
  • Ability to lead continuous quality system improvements for the validation program.
  • Data analysis such as Six-Sigma; ability to work in a cross-functional team environment Note: The above statements are intended to describe the general nature and level of work being performed by the incumbent. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of this position.

Note: The above statements are intended to describe the general nature and level of work being performed by the incumbent. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of this position
WHAT WE OFFER
Mativ benefits say a lot about how we care for each other. Our employees and their families have many different needs. As a result, our benefits offer choices on many levels and are high in quality, competitive in the marketplace, and affordable.
ABOUT MATIV
Mativ Holdings, Inc. is a global leader in specialty materials headquartered in Alpharetta, Georgia. The company connects, protects, and purifies the world every day through a wide range of critical components and engineered solutions that solve our customers' most complex challenges. We manufacture on three continents and generate sales in nearly 100 countries through our family of business-to-business and consumer product brands. The company's two segments, Filtration & Advanced Materials and Sustainable & Adhesive Solutions, target premium applications across diversified and growing end-markets, from filtration to healthcare to sustainable packaging and more. Our broad portfolio of technologies combines polymers, fibers, and resins to optimize the performance of our customers' products across multiple stages of the value chain. Our leading positions are a testament to our best-in-class global manufacturing, supply chain, and materials science capabilities. We drive innovation and enhance performance, finding potential in the impossible.

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