Computer aided design Jobs in Colorado Springs, CO
Create a job alert for this search
Computer aided design • colorado springs co
- New!
Computer System Assurance Consultant
VirtualVocationsColorado Springs, Colorado, United StatesStructural Design Technician
JacobsColorado Springs, CO, United StatesArchitectural Design Intern | Summer 2026
DLR GroupColorado Springs, Colorado, USAIC Design Engineer
Broadcom Inc.USA, Colorado, Colorado Springs, 4420 Arrowswest DriveComputer Repair Technician
CellairisFort Carson, ColoradoCivil Design Intern
Galloway & CompanyColorado Springs, Colorado, USAComputer Engineer - Mid-level
CACI International IncColorado Springs, CO, USSpace Vehicle Concept Design Engineer
The Aerospace CorporationColorado Springs, CO, United StatesLecturer - Computer Science
University of ColoradoColorado Springs, USDigital Design Engineer
Analog DevicesCentennial, Colorado Springs, CO, USRTL Synthesis IC Design Engineer
BroadcomColorado Springs, Colorado, USALead Systems Design Analyst
BoeingColorado Springs, Colorado, USAComputer Vision AI Engineer
Booz Allen HamiltonUSA, CO, Colorado Springs- New!
Design Engineer
ActalentColorado Springs, Colorado, USAtutor - Computer Programming
BUKIColorado Springs, CO, USComputer Scientist
JT4Colorado Springs, CO, USENGINEER, COMPUTER I
Chugach Government Solutions, LLCCOLORADO SPRINGS, Colorado, USDesign Associate
Floor Coverings InternationalColorado Springs, COElectrical Design Engineer
CAESColorado Springs, Colorado, USComputer System Assurance Consultant
VirtualVocationsColorado Springs, Colorado, United States- Full-time
A company is looking for a Computer System Assurance (CSA) Consultant / Senior Validation Engineer.
Key Responsibilities :
Provide CSA / CSV subject matter expertise across PV, Clinical, and Regulatory Affairs platforms
Support system implementations, enhancements, integrations, upgrades, and data migrations from a compliance perspective
Develop and review validation deliverables including Validation Plans, Risk Assessments, and Validation Summary Reports
Required Qualifications :
5-8 years of hands-on experience supporting GxP systems in Pharmacovigilance, Clinical, or Regulatory Affairs
Strong understanding of CSA principles, CSV, and SDLC processes
Experience authoring and / or reviewing validation documentation
Working knowledge of GxP regulations (e.g., FDA, EMA, ICH) and data integrity expectations
Ability to work independently in a fast-paced, matrixed environment