Roles and Responsibilities
Design, develop, test, and maintain computerized systems validation (CSV) processes for medical devices.
Collaborate with cross-functional teams to ensure compliance with regulatory requirements such as 21 CFR Part 11.
Develop and execute test plans, scripts, and reports to validate software applications used in medical device development.
Provide technical support for CSV activities including troubleshooting issues related to data integrity and system functionality.
Ensure timely delivery of high-quality results by managing project timelines and resources effectively.
📌 Opening For Csv Computer System Validation Bangalore ! Bengaluru
🏢 EY
📍 Bengaluru