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

Johnson & Johnson MedTech

Beijing, China
Not specified (assumed hybrid based on industry norms).
Regulatory strategy development
China regulatory systems expertise
Drug development lifecycle management
Johnson & Johnson MedTech is seeking a Senior Manager/Associate Director for Regulatory Affairs focused on Hematology & Oncology Early Development in Beijing, China. The role involves developing regulatory strategies, leading interactions with regulatory agencies, and ensuring compliance for drug development and lifecycle management

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.
  • The position leads China regulatory interactions, drives high-quality submissions and approvals, monitors regulatory changes, and partners closely with R&D and commercial teams to enable successful drug development and commercial continuity.
  • Johnson & Johnson provides an inclusive work environment respecting diversity and dignity, empowering employees to innovate across healthcare solutions.

Matching Summary

Match Score: 85

Johnson & Johnson MedTech is seeking a Senior Manager/Associate Director for Regulatory Affairs focused on Hematology & Oncology Early Development in Beijing, China. The role involves developing regulatory strategies, leading interactions with regulatory agencies, and ensuring compliance for drug development and lifecycle management.

Skills & Requirements

Must-have

  • Regulatory strategy development
  • China regulatory systems expertise
  • Drug development lifecycle management
  • Health authority interactions in China
  • Regulatory submissions and approvals

Nice-to-have

  • Strong collaboration skills
  • Communication and influencing skills
  • Leadership and learning agility
  • Storytelling and presentation abilities
  • Cross-functional team partnership

Key Requirements

  • Master’s degree in life-science discipline
  • More than 5 years regulatory affairs experience
  • Experience in multinational pharmaceutical company
  • Pharmaceutical R&D experience
  • Excellent English communication skills

Work Rights

Not specified

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