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Computer System Validation Engineer Jobs in Dallas, TX

Pacer Group

Non-Product Validation Engineer

Plano, TX · On-site

$33/hr

Monitor and evaluate system performance to ensure continued validated state Required Qualifications: * Bachelor's degree in Engineering, Computer Science, or related technical field * Minimum 5 years ...

Spruce Infotech

Validation Expert

Fort Worth, TX · On-site

Work with project management to build an integrated project plan inclusive of the required Computer System Validation (CSV) Lifecycle Deliverables, quality gates and summarization milestones.

Texas Instruments

Validation Engineer NCG

Dallas, TX · On-site

As a validation engineer, you play a vital role in assuring the quality and performance of TI ... Ability to quickly ramp on new systems and processes * Demonstrated strong interpersonal ...

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All JobsComputer System Validation Engineer JobsComputer System Validation Engineer Jobs in Dallas, TX

Computer System Validation Engineer information

See Dallas, TX salary details

$29

$51

$74

How much do computer system validation engineer jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for computer system validation engineer in Dallas, TX is $51.24, according to ZipRecruiter salary data. Most workers in this role earn between $38.51 and $63.75 per hour, depending on experience, location, and employer.

What are some common challenges faced by Computer System Validation Engineers in regulated industries?

Computer System Validation Engineers often encounter challenges such as keeping up with evolving regulatory requirements, managing documentation for multiple systems, and ensuring timely validation while coordinating with cross-functional teams. Balancing strict compliance with project deadlines can be demanding, especially when systems are complex or legacy infrastructure is involved. Additionally, effective communication with IT, QA, and business stakeholders is essential to address issues quickly and maintain validation standards.

What does a Computer System Validation Engineer do?

A Computer System Validation Engineer is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals or medical devices, meet all required standards for quality, reliability, and compliance. They create and execute validation protocols, document testing procedures, and ensure that systems operate as intended. Their work is critical for meeting regulatory requirements set by agencies like the FDA, and they collaborate closely with IT, quality assurance, and regulatory teams.

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

To thrive as a Computer System Validation Engineer, you need a solid background in computer science or engineering, knowledge of regulatory requirements (such as FDA or GxP), and experience in validation processes. Familiarity with validation tools, quality management systems, and documentation software is typically required, along with certifications like ISPE or ASQ being beneficial. Strong attention to detail, analytical thinking, and effective communication are essential soft skills for coordinating teams and ensuring compliance. These skills and qualities are crucial to ensure that computer systems meet regulatory standards, maintain data integrity, and support business operations in regulated industries.

What is the difference between Computer System Validation Engineer vs Quality Assurance Specialist?

AspectComputer System Validation EngineerQuality Assurance Specialist
CertificationsGAMP, GxP validation certificationsISO, Six Sigma, GMP certifications
Work EnvironmentPharmaceutical, biotech, medical device industriesManufacturing, software, healthcare sectors
Primary FocusValidating computer systems and software complianceEnsuring overall quality and process improvements

The Computer System Validation Engineer primarily focuses on validating computer systems to meet regulatory standards, ensuring software compliance in regulated industries. In contrast, the Quality Assurance Specialist oversees broader quality processes, including audits and process improvements. Both roles require knowledge of industry regulations but differ in scope and specific responsibilities.

What are popular job titles related to Computer System Validation Engineer jobs in Dallas, TX? For Computer System Validation Engineer jobs in Dallas, TX, the most frequently searched job titles are:
What job categories do people searching Computer System Validation Engineer jobs in Dallas, TX look for? The top searched job categories for Computer System Validation Engineer jobs in Dallas, TX are:
Computer System Validation Engineer jobs near you
Infographic showing various Computer System Validation Engineer job openings in Dallas, TX as of June 2026, with employment types broken down into 91% Full Time, 6% Part Time, 2% Contract, and 1% Nights. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $106,587 per year, or $51.2 per hour.

Computer System Validation-Pharmaceutical

PharmEng Technology

Fort Worth, TX

Other

Posted 7 days ago

Job description

Title: Computer Validation Specialist-PQM Location: Fort Worth, TX Company: PharmEng Technology Inc. PharmEng Technology is a full service consulting firm that serves the pharmaceutical, medical devices and biotechnology industries in North America and internationally. Since 1997, the company has provided industry recognized consulting services assisting clients in the rapid commercialization of new product from drug discovery, strategic planning to process scale up.

PharmEng has immediate opening for candidates with experience in Process Validation Engineer. Essential Functions and Responsibilities Proficient in Validation and Qualification aspects of systems. If required, creates and documents Validation Plan, Quality Plan, IQ Report, OQ Report, and Validation Summary Reports.

Drive continuous improvement of the quality system to meet and sustain compliance with internal and external regulatory requirements Conduct Quality reviews to evaluate if processes and deliverables fulfill the requirements for quality, to uncover errors or deficiencies in processes and deliverables, and to identify strengths and opportunities for improvement Follow up resolution of identified quality exposures and escalation to line management if critical situations are not resolved in due course Contribute to business decisions in the decisions in the definition and assessment of IT requirements Support the development and delivery of training in quality matters Drive and facilitate create of relevant of system SOPs. Prepare and follow internal authority inspections. Prepare, or review and approve major system documentation to ensure consistency with quality standards and quality deliverables.

Coordination documentation, testing and change management activities to ensure compliance with business and regulatory needs Develop PQM resources for projects and services and monitor their performance to ensure adherence with agreed quality systems. Forecast demand and plan for IT PQM related to projects, provide task estimating and ICE roadmap to PMs, monitor and manage project risk and compliance Ownership IT CAPA and CCR Process for the responsible functional areas. Minimum Qualifications: Bachelor's of Science and a minimum of 5 years experience in IT in pharmaceutical industry with expert knowledge of current regulations Ability to interact with all levels of the organization Influence and leadership capability, and credibility within the business Strong organization skills Strong written and verbal communication skills Excellent written and spoken English Thank you for your interest in our organization.

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