Computer System Validation Engineer

Consultant, CSV Engineer, Gene Therapy

Summary

The CSV Engineer is responsible for ensuring that GxP computerized systems at our client site are validated in compliance with regulatory standards (21 CFR Part 11, EU Annex 11, GAMP 5).

This role directly supports gene therapy manufacturing operations by leading validation activities for key systems, including Veeva QMS, BMRAM, analytical lab instruments, and the Metasys BMS. By maintaining data integrity and system compliance, the CSV Engineer plays a critical part in ensuring product quality, patient safety, and regulatory inspection readiness.

Duties / Expectations of Role

Author, review, and execute validation deliverables for GxP computerized systems, including Validation Plans, Requirements Specifications (URS/FS/DS), IQ/OQ/PQ protocols, Trace Matrices, and Validation Summary Reports.

Support computer system validation efforts for Veeva Vault QMS, BMRAM (laboratory information management), analytical lab instruments (e.g., HPLC, UHPLC, PCR instruments, plate readers etc.), ERP System (NetSuite).

Perform risk assessments to determine validation approach and ensure appropriate testing of system functionality, data integrity, and audit trail review.

Manage system change control, deviations, and CAPAs related to validated systems, ensuring compliance with Forge’s quality system.

Collaborate with IT, QA, Lab Operations, and Facilities teams to support system upgrades, patches, and periodic reviews while maintaining a validated state.

Mandatory Requirements

Bachelor’s degree in Computer Science, Engineering, Life Sciences, or related field (or equivalent experience).

5-7+ years of experience in Computer System Validation (CSV) within a GxP regulated environment (pharmaceutical, biotech, or medical device).

Working knowledge of GAMP 5, 21 CFR Part 11, EU Annex 11, and data integrity principles (ALCOA+).

Experience validating at least one of the following: Veeva Vault QMS, BMRAM, laboratory instrumentation (e.g., Waters, Agilent, Chromeleon, Softmax or similar), or a building management system (BMS) like Metasys.

Strong technical writing skills and ability to execute protocols with minimal supervision.

Ability to work onsite (in Columbus, Ohio) Hybrid 2-3 days/week on average (depending on site needs).

Nice to Have

BMRAM

Analytical lab instruments

Term & Start

6 Month project with strong possibility of extension.

Start Date Mid-July 2026

Hybrid 70% Remote / 30% Onsite Columbus, OH

Full time (40 hours/week