Associate Director, Eucan Regulatory Lead - Gi And Inflammation

Takeda

Zurich, Switzerland
Fully remote
Regulatory submissions management
Experience with health authorities
Drug regulatory affairs expertise
At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients

Job Summary

  • At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients.
  • You will lead regional regulatory strategy for assigned assets, driving submission excellence across development, registration, and life-cycle management to enable timely patient access.
  • This role involves effectively communicating regulatory strategies and providing tactical advice for product development.

Matching Summary

At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients.

Skills & Requirements

Must-have

  • Regulatory submissions management
  • Experience with Health Authorities
  • Drug regulatory affairs expertise

Nice-to-have

  • Strong communication skills
  • Ability to adapt to change
  • Mentorship and team development

Key Requirements

  • Minimum 8 years of experience
  • Advanced scientific related degree preferred
  • Solid regulatory experience in EU/GEM region

Work Rights

Not specified

Tailored Resume

Cover Letter