APAC Regulatory Strategy Director, Hematology

Biopharma Asia; Singapore; On-site; SGD 180,000 - 280,000; Full time

Job summary

Johnson & Johnson in Singapore seeks a Regional Regulatory Leader for Asia Pacific to define and implement regional regulatory strategy for assigned therapeutic areas, aligning with global plans and leading interactions with health authorities across AP. The role coordinates with local affiliates, C-ROSS teams, and launch readiness to drive timely approvals.

You will manage teams, budgets, and career development, shaping regulatory strategy to accelerate approvals, ensuring lifecycle management

Qualifications

• Minimum of bachelor’s degree or equivalent in pharmacy or life-science or health-related discipline.
• Minimum of 10–12 years of overall experience, including at least 5 years in regulatory experience.
• Hands-on experience in pharmaceutical product registration in AP countries.
• Demonstrated leadership and contribution to drug development strategies.
• Ability to handle multiple projects and work cross-functionally.
• Excellent verbal and written communication skills; English proficiency required.

Responsibilities

• Develops regional regulatory strategy for assigned TA/products.
• Leads regulatory submissions and lifecycle management across AP.
• Interacts with Health Authorities and local operating companies.
• Mentors/regulates regulatory staff and develops talent within the team.
• Ensures budget, performance, and compliance for the regulatory group.

Skills

Leadership

Regulatory strategy

Communication

Project management

Regulatory submissions

Team coaching

Education

Bachelor’s degree in pharmacy or life-science

Masters/PharmD

PhD (preferred)

Tools

MS Office

Job description

Johnson & Johnson in Singapore seeks a Regional Regulatory Leader for Asia Pacific to define and implement regional regulatory strategy for assigned therapeutic areas, aligning with global plans and leading interactions with health authorities across AP. The role coordinates with local affiliates, C-ROSS teams, and launch readiness to drive timely approvals.

You will manage teams, budgets, and career development, shaping regulatory strategy to accelerate approvals, ensuring lifecycle management