Head of Regulatory Affairs, APAC

BEONE MEDICINES SINGAPORE PTE. LTD.

Singapore
Not specified (assumed flexible based on location).
12 years biotechnology or pharmaceutical experience
8 years regulatory leadership capacity
Broad background in oncology
BeOne Medicines Singapore Pte. Ltd. is seeking a Head of Regulatory Affairs for the Asia Pacific region, responsible for developing and executing regulatory strategies to ensure market access for their products. The role involves leading a team of regulatory professionals and collaborating with global functions, with a focus on oncology and inflammation

Job Summary

  • The Head of Regulatory Affairs will develop and implement APAC regulatory strategies to secure market access for products in hematology, solid tumours, and inflammation & immunology.
  • This role requires leading a regional team of regulatory professionals while managing budgets, timelines, and external vendor relationships to support compounds through all development phases.
  • The successful candidate must have extensive experience in oncology and demonstrate strong leadership abilities to integrate regulatory strategy with global and local business objectives.

Matching Summary

Match Score: 85

BeOne Medicines Singapore Pte. Ltd. is seeking a Head of Regulatory Affairs for the Asia Pacific region, responsible for developing and executing regulatory strategies to ensure market access for their products. The role involves leading a team of regulatory professionals and collaborating with global functions, with a focus on oncology and inflammation.

Skills & Requirements

Must-have

  • 12 years biotechnology or pharmaceutical experience
  • 8 years regulatory leadership capacity
  • Broad background in oncology
  • Experience with small molecules and biologics
  • Leading multiple Health Agency interactions
  • Managerial and collaboration ability

Nice-to-have

  • Knowledge of Inflammation and Immunology
  • Experience working as lead in two major APAC areas
  • Experience in multinational pharmaceutical company
  • Veeva regulatory publishing skills

Key Requirements

  • Minimum 12 years in biotech/pharma industry
  • Minimum 8 years in regulatory leadership
  • Demonstrable success in APAC regulatory approvals
  • Experience with small molecules and biologics
  • Proven managerial and cross-functional collaboration skills

Work Rights

Not specified

Tailored Resume

Cover Letter