Description:
Role name: Validation Engineer Location: Sunnyvale/ Santa Clara, CA Duration: 6 Months Must have skills: Computer System Validation, 21 CFR Part 11, GxP, FDA, 21 CFR Part 11, ISO 13485, IEC 62304 Role Description: Develop, implement, and maintain software quality assurance processes for non-product software used in medical device development.Ensure adherence to regulatory standards (FDA, ISO 13485, IEC 62304) and industry best practices for non-product software.Support audits and inspections by
Jul 17, 2025;
from:
dice.com