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