Computer System Validation Engineer

Confirmed live in the last 24 hours

ALTEN Technology USA

Compensation

$95,000 - 110,000

Irvine, California, United States

On-site

Posted November 13, 2025

Job Description

We’re ALTEN Technology USA, an engineering company helping clients bring groundbreaking ideas to life—from advancing space exploration and life-saving medical devices to building autonomous electric vehicles. With 3,000+ experts across North America, we partner with leading companies in aerospace, medical devices, robotics, automotive, commercial vehicles, EVs, rail, and more.

As part of the global ALTEN Group—57,000+ engineers in 30 countries—we deliver across the entire product development cycle, from consulting to full project outsourcing.

When you join ALTEN Technology USA, you’ll collaborate on some of the world’s toughest engineering challenges, supported by mentorship, career growth opportunities, and comprehensive benefits. We take pride in fostering a culture where employees feel valued, supported, and inspired to grow.

Position Summary

The Computer System Validation (CSV) Engineer II will ensure compliance of computerized systems within a pharmaceutical manufacturing environment. This role focuses on the development, execution, and closure of Installation, Operational, and Qualification (IOQ) protocols for critical systems, including SCADA and Manufacturing Execution Systems (MES). The engineer will work in a cleanroom environment alongside manufacturing equipment to support system qualification activities in accordance with regulatory requirements (FDA, EU GMP, GAMP 5).

Responsibilities

Develop and author IOQ protocols for computerized systems, ensuring alignment with user requirements and regulatory standards.
Execute IOQ protocols in a cleanroom environment, coordinating with cross-functional teams (Engineering, QA, Manufacturing).
Perform data collection, deviation management, and ensure timely resolution of discrepancies during qualification activities.
Generate and finalize IOQ reports, ensuring complete documentation and compliance with internal SOPs and industry guidelines.
Support the qualification of iFIX SCADA system and related MES components for manufacturing operations.
Collaborate with IT and Automation teams to ensure system configurations meet validation requirements.
Maintain validation documentation in compliance with FDA 21 CFR Part 11 and other applicable regulations.
Participate in risk assessments and impact analyses for system changes.