Description:
Key Responsibilities:Manage and oversee multiple projects across the MedTech portfolio, ensuring alignment with organizational goals and regulatory requirements. Implement and maintain Design Control processes throughout the product development lifecycle. Ensure project documentation and activities comply with 21 CFR Part 820, ISO 13485, IEC 62304, and ISO 14971 standards. Coordinate with cross-functional teams including R&D, Quality, Regulatory Affairs, and Manufacturing to ensure project miles
Oct 28, 2025;
from:
dice.com