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Validation Jobs in Dallas, TX (NOW HIRING)

The AVP, Model Validation is responsible for model validation and ensure they are meeting Model Risk Management policies, standards, procedures as well as regulations (OCC2011-12/SR 11-7). This role ...

The Milestone & Validation Specialist will be responsible for assisting the Milestone and Validation Lead in implementing the project plan to ensure it stays within the established milestones ...

The Milestone & Validation Specialist will be responsible for assisting the Milestone and Validation Lead in implementing the project plan to ensure it stays within the established milestones ...

The AVP, Model Validation is responsible for model validation and ensure they are meeting Model Risk Management policies, standards, procedures as well as regulations (OCC2011-12/SR 11-7). This role ...

The Milestone-Validation Lead is responsible for maintaining construction inspection checklists status and scheduling inspections and coordinating with city authorities, third parties, investment ...

The Milestone-Validation Lead is responsible for maintaining construction inspection checklists status and scheduling inspections and coordinating with city authorities, third parties, investment ...

Senior Engineer, Process Validation

Dallas, TX ยท On-site +1

$100K - $130K/yr

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 ...

Senior Engineer, Process Validation

Dallas, TX ยท On-site +1

$100K - $130K/yr

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 ...

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Validation information

See Dallas, TX salary details

$22

$51

$77

How much do validation jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for validation in Dallas, TX is $51.44, according to ZipRecruiter salary data. Most workers in this role earn between $38.99 and $62.55 per hour, depending on experience, location, and employer.

What is the difference between Validation vs Quality Assurance?

AspectValidationQuality Assurance
PurposeEnsures products meet specifications and intended usePrevents defects through process improvements
FocusProduct-specific testing and verificationProcess and system quality control
ActivitiesDesign validation, process validation, equipment validationAudits, process reviews, standards compliance
TimingBefore product releaseThroughout production cycle

Validation focuses on confirming that a product or process meets specified requirements before release, while Quality Assurance emphasizes maintaining quality standards throughout the production process to prevent defects. Both roles are essential in industries like pharmaceuticals and manufacturing, but they serve different stages of quality management.

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 or life sciences, with expertise in quality assurance and regulatory compliance. Familiarity with validation protocols, statistical analysis tools, and industry standards such as GMP, FDA, or ISO guidelines is essential. Strong analytical thinking, attention to detail, and effective communication skills help you identify issues and collaborate across teams. These abilities ensure that products and processes meet strict safety and quality requirements, minimizing risks and ensuring regulatory approval.

What are some common challenges faced by professionals in validation roles, and how can they be overcome?

Professionals in validation roles often face challenges such as tight project timelines, evolving regulatory requirements, and the need for meticulous documentation. Balancing thoroughness with efficiency is crucial, as validation processes must be both comprehensive and timely to support product launches or regulatory submissions. Effective communication with cross-functional teams, proactive planning, and staying updated with industry standards can help overcome these challenges and ensure successful validation outcomes.

What is a validation job?

Validation jobs involve ensuring that products, processes, or systems meet specific requirements and function as intended. In industries like pharmaceuticals, biotechnology, and manufacturing, validation specialists test equipment, procedures, and software to guarantee quality and compliance with regulatory standards. These professionals document their findings and help identify areas for improvement, playing a key role in quality assurance. Validation jobs are essential for maintaining product safety, effectiveness, and meeting industry regulations.
What are the most commonly searched types of Validation jobs in Dallas, TX? The most popular types of Validation jobs in Dallas, TX are:
What cities near Dallas, TX are hiring for Validation jobs? Cities near Dallas, TX with the most Validation job openings:
Infographic showing various Validation job openings in Dallas, TX as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 4% Part Time, 1% Temporary, and 6% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $106,988 per year, or $51.4 per hour.

Validation Engineer

Stark Pharma Solutions Inc

Fort Worth, TX โ€ข On-site

Contractor

Re-posted yesterday


Job description

Job Title: Validation Engineer

Location: Fort Worth, TX (Local candidates only)

Travel: Required – Alabama (3–4 weeks, expenses paid)

Duration: 3–6 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