Validation Engineer

We are seeking an experienced Computer System Validation (CSV) Engineer to support validation activities within a regulated pharmaceutical environment. This role will focus on validating Veeva Quality Vault and ensuring compliance with GxP, FDA, and industry standards. Key Responsibilities Support end-to-end validation of Veeva Quality Vault , including new implementations, releases, and enhancements. Conduct risk assessments for system upgrades and change controls to determine appropriate validation scope. Develop and maintain CSV documentation, including: Validation Plans URS (User Requirement Specifications) Traceability Matrices IQ/OQ/PQ Protocols & Test Scripts Summary & Final Validation Reports Collaborate with system owners, QA, IT, and process owners to define validation requirements. Ensure compliance with 21 CFR Part 11 , GxP guidelines, GAMP 5, and internal quality procedures. Support audits, system releases, and change management activities. Required Skills & Experience Previous experience as a Quality CSV Engineer/Consultant in a pharmaceutical setting. Hands‑on experience validating Veeva Quality Vault (Quality Docs, QMS, Training, etc.). Strong understanding of CSV lifecycle, risk-based validation, and regulatory compliance. Ability to create high-quality validation documentation (VP, URS, TM, IQ/OQ/PQ). Excellent communication skills and experience working cross‑functionally with QA, IT, and business teams. Seniority level Mid‑Senior level Employment type Contract Job function Pharmaceutical Manufacturing and Biotechnology Research San Francisco, CA $99,500.00-$200,000.00 2 days ago #J-18808-Ljbffr United Pharma Technologies Inc