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Computer Validation Jobs in Denton, 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.

Bachelor's degree in Engineering, Computer Science, or related technical field * Minimum 5 years of experience in software validation within a regulated medical device environment * Demonstrated ...

The Model Validation Director is expected to lead and execute model validation testing processes on ... Computer Science, Management Information Systems, or Statistics/Mathematics. * Experience with data ...

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Computer Validation information

See Denton, TX salary details

$9

$50

$80

How much do computer validation jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for computer validation in Denton, TX is $50.93, according to ZipRecruiter salary data. Most workers in this role earn between $39.23 and $60.38 per hour, depending on experience, location, and employer.

Can computer engineers make $500,000?

Computer validation professionals typically do not earn $500,000 annually, as this level of compensation is uncommon in the field. High salaries may be possible for senior roles, especially in biotech or pharmaceutical industries, or with extensive experience, specialized skills, and leadership responsibilities. Most salaries for computer validation roles range from $70,000 to $150,000 per year.

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

AspectComputer ValidationQuality Assurance Specialist
Required CredentialsGxP, 21 CFR Part 11, validation certificationsISO standards, QA certifications, GxP knowledge
Work EnvironmentPharmaceutical, biotech, regulated industriesManufacturing, healthcare, regulated industries
Employer & Industry UsageRegulated industries requiring validated systemsEnsuring quality compliance across processes

Computer Validation focuses on verifying that computer systems meet regulatory requirements and function correctly, primarily in regulated industries. Quality Assurance Specialists oversee overall quality processes, ensuring compliance and standards across various operations. While both roles require knowledge of GxP and industry regulations, Computer Validation is more technical and system-specific, whereas QA Specialists have a broader scope in quality management.

What is the salary of a CSV engineer?

A CSV (Computer System Validation) engineer's salary typically ranges from $70,000 to $120,000 annually, depending on experience, location, and certifications. Senior roles or those with specialized skills in validation tools and regulatory compliance may earn higher salaries.

Is computer system validation a good field?

Computer validation professionals ensure that computer systems in regulated industries meet quality and compliance standards, often working with tools like GxP and validation protocols. The field offers steady demand, especially in pharmaceuticals and biotech, and requires knowledge of regulatory requirements and validation processes. It can be a rewarding career for those interested in quality assurance, compliance, and technical problem-solving.

Is CSV a skill?

In the context of computer validation, familiarity with CSV (comma-separated values) files is considered a useful technical skill, as it involves working with data formats and data management tools. Proficiency in handling CSV files can support tasks such as data import/export, validation, and reporting. However, CSV itself is a data format, not a standalone skill, but understanding how to work with it is valuable for validation professionals.
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What cities near Denton, TX are hiring for Computer Validation jobs? Cities near Denton, TX with the most Computer Validation job openings:
Infographic showing various Computer Validation job openings in Denton, TX as of June 2026, with employment types broken down into 50% Full Time, 23% Part Time, and 27% Contract. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $105,934 per year, or $50.9 per hour.

Computer System Validation-Pharmaceutical

PharmEng Technology

Fort Worth, TX โ€ข On-site

Other

Posted 9 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.