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Computer System Validation Jobs in Dallas, TX (NOW HIRING)

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.

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 ...

... Computer Science, Information Technology, Electronics Engineering, or a related field Minimum 5-8 ... computerized system validation (CSV) approaches for non-product applications Proficiency in ...

Warehouse Clerk

Dallas, TX · On-site

$16 - $17/hr

Experience with receiving raw materials; unpacking, count verification, computer system validation, packing list verification. * Experience driving a forklift and transporting materials within a ...

Warehouse Clerk

Dallas, TX · On-site

$16 - $17/hr

Experience with receiving raw materials; unpacking, count verification, computer system validation, packing list verification. * Experience driving a forklift and transporting materials within a ...

Senior System SW validation engineer * Lead software and system validation planning and execution ... Bachelor's or Master's degree in Electronics Engineering, Computer Science or Computer Engineering ...

Oversee new system installation and setup and customize them for business needs. * Run tests on ... Ability to define problems, collect data, establish facts, and draw valid conclusions. * Work well ...

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Computer System Validation information

See Dallas, TX salary details

$10

$53

$85

How much do computer system validation jobs pay per hour?

As of Jun 1, 2026, the average hourly pay for computer system validation in Dallas, TX is $53.73, according to ZipRecruiter salary data. Most workers in this role earn between $41.39 and $63.75 per hour, depending on experience, location, and employer.

What is a Computer System Validation job?

A Computer System Validation (CSV) job involves ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, meet compliance and regulatory requirements. CSV professionals develop and execute validation protocols to confirm that software, hardware, and processes function as intended and maintain data integrity. They work with quality assurance, IT, and regulatory teams to document compliance with standards like FDA 21 CFR Part 11 and GxP. This role is critical in maintaining system reliability, product quality, and patient safety.

What are the key skills and qualifications needed to thrive in the Computer System Validation position, and why are they important?

To excel in Computer System Validation, candidates typically need a background in computer science, engineering, or life sciences, with expertise in validating software and systems in regulated environments such as pharmaceuticals or medical devices. Familiarity with tools like validation documentation software, GAMP 5 guidelines, FDA 21 CFR Part 11 regulations, and potentially certifications like CSV Professional or Six Sigma is highly valued. Strong attention to detail, analytical thinking, and effective communication skills help professionals work collaboratively and document findings precisely. These abilities ensure compliance, data integrity, and the reliability of computerized systems critical to safety and quality.

What are some typical challenges faced in Computer System Validation roles?

Professionals in Computer System Validation often encounter challenges such as keeping up with evolving regulatory requirements, ensuring complete and accurate documentation, and coordinating with cross-functional teams to implement validation protocols. Balancing thoroughness with project deadlines can also be demanding, as every validation step must stand up to external audits. However, these challenges provide valuable experience, strengthen project management abilities, and emphasize teamwork—key attributes that support career advancement into validation leadership or quality assurance roles.
What are the most commonly searched types of Computer System Validation jobs in Dallas, TX? The most popular types of Computer System Validation jobs in Dallas, TX are:
What are popular job titles related to Computer System Validation jobs in Dallas, TX? For Computer System Validation jobs in Dallas, TX, the most frequently searched job titles are:
What job categories do people searching Computer System Validation jobs in Dallas, TX look for? The top searched job categories for Computer System Validation jobs in Dallas, TX are:
What cities near Dallas, TX are hiring for Computer System Validation jobs? Cities near Dallas, TX with the most Computer System Validation job openings:
Infographic showing various Computer System Validation job openings in Dallas, TX as of May 2026, with employment types broken down into 84% Full Time, 4% Part Time, and 12% Contract. Highlights an 100% In-person job distribution, with an average salary of $111,766 per year, or $53.7 per hour.

Computer System Validation-Pharmaceutical

PharmEng Technology

Fort Worth, TX

Other

Posted 28 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.

However, only those selected will be contacted for an interview.