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Validation Engineer Jobs in Dallas, TX (NOW HIRING)

As a validation engineer, you play a vital role in assuring the quality and performance of TI's innovative IC products. In this role, you'll support the development and implementation of strategies ...

As a validation engineer, you play a vital role in assuring the quality and performance of TI's innovative IC products. In this role, you'll support the development and implementation of strategies ...

Senior System Validation Engineer DUTIES: Validating complex embedded software interactions spanning propulsion, ADAS/AD, body, infotainment, and connected services. Lead integration and validation ...

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Validation Engineer information

See Dallas, TX salary details

$22

$51

$77

How much do validation engineer jobs pay per hour?

As of Jul 28, 2026, the average hourly pay for validation engineer in Dallas, TX is $51.46, according to ZipRecruiter salary data. Most workers in this role earn between $39.04 and $62.60 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 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.

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 are Validation Engineers?

Validation Engineers are professionals responsible for ensuring that systems, processes, or equipment meet regulatory standards and function as intended. They typically work in industries such as pharmaceuticals, biotechnology, manufacturing, and medical devices. Their duties involve creating validation protocols, conducting tests, analyzing data, and documenting results to ensure compliance with industry regulations and quality standards. Validation Engineers play a critical role in maintaining product safety and efficacy, as well as helping companies pass audits and inspections.
What are the most commonly searched types of Validation Engineer jobs in Dallas, TX? The most popular types of Validation Engineer jobs in Dallas, TX are:
What are popular job titles related to Validation Engineer jobs in Dallas, TX? For Validation Engineer jobs in Dallas, TX, the most frequently searched job titles are:
What cities near Dallas, TX are hiring for Validation Engineer jobs? Cities near Dallas, TX with the most Validation Engineer job openings:
Infographic showing various Validation Engineer job openings in Dallas, TX as of July 2026, with employment types broken down into 77% Full Time, 4% Part Time, 2% Temporary, and 17% Contract. Highlights an 96% In-person, and 4% Remote job distribution, with an average salary of $107,046 per year, or $51.5 per hour.

Validation Engineer

Stark Pharma Solutions Inc

Fort Worth, TX โ€ข On-site

Contractor

Posted 17 days ago


Job description

Job Title: Validation Engineer

Location: Fort Worth, TX (Local candidates only)

Travel: Required โ€“ Alabama (3โ€“4 weeks, expenses paid)

Duration: 3โ€“6 Month Contract

Start Date: Immediate

Job Summary

We are seeking a Validation Engineer to support EO sterilization validation activities within a regulated manufacturing environment. This role will focus on supervising and coordinating Performance Qualification (PQ) execution activities while ensuring compliance with GMP and ALCOA+ documentation standards.

The ideal candidate will have hands-on experience with sterilization validation processes, strong coordination skills, and the ability to support cross-functional execution activities in a fast-paced environment.

Key Responsibilities

  • Supervise execution of EO sterilization Performance Qualification (PQ) activities
  • Coordinate half-cycle, nominal/full-cycle, and maximum-cycle sterilization runs
  • Prepare and manage PCDs (Process Challenge Devices) and Biological Indicators (BIs) for shipment and cycle insertion
  • Support preparation and arrangement of dunnage for EO sterilization processes
  • Oversee movement of product loads through refrigerated storage, tempering, sterilization, and aeration processes
  • Coordinate retrieval and shipment of PCDs, BIs, and product samples for Quality Control testing
  • Ensure execution activities and documentation comply with ALCOA+ principles and GMP requirements
  • Collaborate with Validation, Quality, and Operations teams to support project timelines and execution

Required Qualifications

  • Experience in validation within medical device, pharmaceutical, or regulated manufacturing environments
  • Hands-on knowledge of EO sterilization validation and PQ execution activities
  • Strong understanding of GMP documentation practices and ALCOA+ principles
  • Ability to coordinate cross-functional activities and manage execution timelines
  • Strong communication and organizational skills