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Computer System Validation Csv Jobs in Texas (NOW HIRING)

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.

Arthur Lawrence

CQV Engineer

College Station, TX · On-site

Strong experience with computerized systems validation (CSV), validation lifecycle documentation (URS, FRS, DS, IQ, OQ, PQ, RTM, Validation Reports), and quality. * Proven ability to lead cross ...

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Computer System Validation Csv information

See Texas salary details

$27

$48

$70

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

As of Jul 1, 2026, the average hourly pay for computer system validation csv in Texas is $48.26, according to ZipRecruiter salary data. Most workers in this role earn between $36.30 and $60.00 per hour, depending on experience, location, and employer.

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

To thrive as a Computer System Validation (CSV) professional, you need a solid understanding of computer science, regulatory compliance (such as FDA 21 CFR Part 11), and validation methodology, often supported by a degree in a scientific or technical field. Familiarity with documentation tools, validation protocols, and quality management systems, as well as certifications like PMP or Six Sigma, is highly beneficial. Strong attention to detail, problem-solving abilities, and effective communication skills enable effective cross-functional collaboration. Mastering these skills ensures accurate validation processes, regulatory compliance, and smooth project execution in highly regulated environments.

What is a Computer System Validation (CSV) job?

A Computer System Validation (CSV) job involves ensuring that computerized systems used in regulated industries, such as pharmaceuticals and medical devices, comply with industry standards and regulatory requirements (e.g., FDA 21 CFR Part 11, GxP). CSV professionals develop validation protocols, conduct testing, and document system performance to ensure data integrity, reliability, and compliance. Their role is critical in maintaining system quality and avoiding regulatory risks.

What are some typical challenges faced by Computer System Validation professionals and how are they addressed?

Computer System Validation (CSV) professionals often encounter challenges such as keeping up with evolving regulations, managing complex documentation requirements, and ensuring robust communication between IT, quality assurance, and business teams. Navigating system upgrades while maintaining compliance with strict regulatory standards requires careful planning and thorough risk assessment. Successful candidates address these challenges by staying current with industry guidance, utilizing validation templates and checklists, and fostering strong teamwork across various departments. Building collaborative relationships and maintaining meticulous records help ensure both audit readiness and smooth project completion.

What are the most commonly searched types of Computer System Validation Csv jobs in Texas? The most popular types of Computer System Validation Csv jobs in Texas are:
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Computer System Validation Csv jobs near you
Infographic showing various Computer System Validation Csv job openings in Texas as of June 2026, with employment types broken down into 95% Full Time, 3% Part Time, and 2% Nights. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $100,383 per year, or $48.3 per hour.
Validation Expert

Validation Expert

Spruce Infotech

Fort Worth, TX • On-site

Contractor

Posted 7 days ago

Job description

We are looking for people who have demonstrated proven success in roles and through abilities in Computerized System Validation for R&D applications, Risk management and Quality Management.
  • 15+ yrs of professional experience in Life Sciences industry working for a consulting services organization and/or industry experience.
  • Understanding of key pharmaceutical compliance regulations like Computerized System Validation, 21 CFR Part 11, GxP, GAMP 5, Data Privacy, Data Integrity and Information Security
  • Develop and document the validation strategy and approach for the Software Development Lifecycle Activities (SDLC) for the global implementation of R&D systems considering GxP & Non GxP elements and recommend for risk-based testing approach as required.
  • Work with Client Q&C to ensure system compliance with internal policies, procedures, guidelines, and applicable health authority regulations and provide improvement plan to streamline practices, and revise CSV related SOPs as necessary.
  • 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.
  • Knowledge on basic functions on R&D systems
  • Knowledge of various tools/applications like JIRA, HP ALM, Qtest
  • Successful track record using Lean/Agile approaches to validate assets
  • Proven ability in handling multiple large projects, respond quickly to changing situations in complex environments

Preferable IT background to understand larger impact of architecture / technical complexities on the program

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