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# CSV Engineer (Pharmaceuticals)

- **Company:** Digital Intelligence Systems, LLC
- **Location:** Bothell, WA, United States
- **Salary:** $145,600.0 - $164,320.0
- **Contract:** Temporary contract
- **Skills:** Oracle (Applications), SAP (Applications), Software Requirements Analysis, System Testing, Test Execution Engine, Iq/oq/pq, Test Scripts, Syncade, Veeva, GXP, Servicenow
- **Published:** June 17, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=7eff9ac6fa4bc082

## About the Role

* Experience in a GMP manufacturing environment
 * Strong understanding of Good Manufacturing Practices (GMP) and SOP adherence
 * Experience working with GxP regulated systems
 * Knowledge of Computer System Validation (CSV) principles
 * Ability to work in a structured, regulated production environment (including cleanroom compliance if applicable)

Nice-to-Have Qualifications

 * Experience with MES systems (e.g., Emerson Syncade)
 * Experience with ERP systems (SAP or Oracle)
 * Exposure to Electronic Batch Records (EBR) systems (e.g., InfoBatch)
 * Experience with Veeva or ServiceNow platforms

## Description

We are seeking a CSV / Validation Engineer to support validation activities for GxP computerized systems in a GMP manufacturing environment. The role focuses on ensuring compliance of Manufacturing Execution Systems (MES), ERP systems, and other regulated applications throughout the system lifecycle.

The ideal candidate will work closely with Business Owners, Technical Owners, and Quality teams to deliver and maintain validation documentation in alignment with regulatory requirements and internal procedures., * Author, review, and approve Computer System Validation (CSV) documentation

 * Support test execution activities (IQ/OQ/PQ), including documenting test results and deviations
 * Collaborate with Business and Technical Owners to define system requirements and specifications for GxP systems
 * Ensure validation activities comply with GMP, SOPs, and regulatory expectations
 * Maintain traceability matrices, validation plans, test scripts, and summary reports
 * Support validation lifecycle activities for MES, ERP, and EBR systems
 * Ensure all deliverables are inspection/audit ready


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