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Director Computer System Validation Csv Jobs in Texas

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.

Sun-IT Solutions

OT Security Architect

Bedford, TX · On-site

$57.50 - $74.50/hr

Support Computer System Validation (CSV) documentation (URS, FS, DS, IQ, OQ, PQ). * Experience defining patch management and vulnerability management processes for validated OT systems. * Excellent ...

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Deloitte

System Test and Validation Lead

Westlake, TX · On-site +1

Bachelor's degree in business, information systems, computer science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment ...

Deloitte

System Test and Validation Lead

Austin, TX · On-site +1

Bachelor's degree in business, information systems, computer science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment ...

Deloitte

System Test and Validation Lead

Austin, TX · On-site +1

Bachelor's degree in business, information systems, computer science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment ...

Deloitte

System Test and Validation Lead

Dallas, TX · On-site +1

Bachelor's degree in business, information systems, computer science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment ...

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Director Computer System Validation Csv jobs near you
Infographic showing various Director Computer System Validation Csv job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution.

Validation Expert

Spruce Infotech

Fort Worth, TX • On-site

Contractor

Re-posted 14 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

Apply