Bachelor's degree in Computer Science, Engineering, Life Sciences, or related field (or equivalent experience)
5-7+ years of Computer System Validation (CSV) experience in a GxP regulated environment
Strong understanding of GAMP 5, 21 CFR Part 11, EU Annex 11, and data integrity principles
Experience validating systems such as Veeva Vault QMS, BMRAM, or lab instruments
Proficient technical writing and ability to manage validation protocols independently
Responsibilities
Author and execute validation deliverables for GxP computerized systems
Support validation efforts for key systems like Veeva Vault QMS and laboratory instruments
Conduct risk assessments to establish validation strategies
Manage change control, deviations, and CAPAs for validated systems
Collaborate with multidisciplinary teams for system upgrades and compliance
Benefits
Health, dental, and vision insurance
401(k) retirement plan options
Professional development opportunities
Flexible working hours and a supportive work environment
Employee wellness programs
Full Job Description
Job Description:
The CSV Engineer is responsible for ensuring that GxP computerized systems at the 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 Client.
By maintaining data integrity and system compliance, the CSV Engineer plays a critical part in ensuring product quality, patient safety, and regulatory inspection readiness.
Roles & Responsibilities:
uthor, 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.
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 (Client) like Metasys.
Strong technical writing skills and ability to execute protocols with minimal supervision.
Nice to have: BMRAM and analytical lab instruments experience.
