Senior Manager/associate Director, Regulatory Affairs - Hematology & Oncology Early Development Ta

Johnson & Johnson

Beijing, China
Not specified (assumed to be office-based given the location)
Hematology & oncology early development
China regulatory strategy and execution
Lead china regulatory interactions
Johnson & Johnson is seeking a Senior Manager/Associate Director for Regulatory Affairs in Hematology & Oncology Early Development in Beijing, China. The role involves leading regulatory strategy, compliance, and interactions with health authorities to support drug development and commercialization

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 leading China regulatory interactions, driving high-quality submissions and approvals, monitoring regulatory changes, and mitigating regulatory risks.
  • The position requires 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 involves leading regulatory strategy, compliance, and interactions with health authorities to support drug development and commercialization.

Skills & Requirements

Must-have

  • Hematology & Oncology early development
  • China regulatory strategy and execution
  • Lead China regulatory interactions
  • Develop and implement regulatory strategies
  • Prepare and deliver high-quality submissions

Nice-to-have

  • Growth mindset
  • Strong collaboration and influencing skills
  • Demonstrated leadership and learning agility
  • Excellent English communication skills

Key Requirements

  • Master’s degree or above in life-science discipline
  • More than 5 years of regulatory affairs experience
  • Experience in pharmaceutical R&D
  • Strong familiarity with China regulatory systems

Work Rights

Not specified

Tailored Resume

Cover Letter