Senior Manager/associate Director, Regulatory Affairs - Hematology & Oncology Early Development Ta
Johnson & Johnson Innovative Medicine
Beijing, China
Not specified (assumed to be hybrid based on the nature of the role and company culture).
Regulatory strategy and execution
China regulatory agencies
Drug development registration
Johnson & Johnson is seeking a Senior Manager/Associate Director for Regulatory Affairs in Hematology & Oncology Early Development in Beijing, China. The role focuses on developing and executing regulatory strategies, managing submissions, and ensuring compliance with Chinese regulatory requirements
Job Summary
This role is responsible for end-to-end regulatory strategy and execution for new asset development and lifecycle management in Hematology/Oncology early development TA in China.
Key responsibilities include developing and implementing optimal regulatory strategies, preparing and delivering high-quality submissions, and serving as the primary liaison with China regulatory agencies.
The position requires strong collaboration with R&D, QA/Compliance, Supply Chain and Commercial teams to support drug development, registration, launch and lifecycle activities.
Matching Summary
Match Score: 85
Johnson & Johnson is seeking a Senior Manager/Associate Director for Regulatory Affairs in Hematology & Oncology Early Development in Beijing, China. The role focuses on developing and executing regulatory strategies, managing submissions, and ensuring compliance with Chinese regulatory requirements.
Skills & Requirements
Must-have
Regulatory strategy and execution
China regulatory agencies
Drug development registration
Lifecycle management
Cross-functional team collaboration
Nice-to-have
Growth mindset
Learning agility
Story telling and presentation abilities
Key Requirements
Master’s degree or above
More than 5 years of regulatory affairs experience