Regulatory Affairs Specialist (NMPA)

📋 Description Act as RA lead for China product registrations (RA Lead/PM) Coordinate regulatory/clinical strategy and timelines for NMPA submissions Manage registration trackers and the China Regulatory Project Executive Summary Support cross-functional teams, audits, and China localization projects 🎯 Requirements Hybrid onsite weekly in Sunnyvale, CA Mandarin Chinese required 3+ years RA experience 1+ year NMPA regulatory experience (China GB/YY and US FDA) Education: BS/BE in life science; advanced degree preferred Cross-functional collaboration and strong project management skills