Associate Director, Eucan Regulatory Lead - Gi And Inflammation

Takeda UK

Zurich, Switzerland
Fully remote
8 years of experience in drug regulatory affairs
Solid regulatory experience in eu/gem
Ability to manage regulatory submissions
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.
  • You will define and communicate regulatory strategies, submission plans, and timelines, while proactively assessing regulatory risks and the impact of evolving requirements.

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

  • 8 years of experience in drug regulatory affairs
  • Solid regulatory experience in EU/GEM
  • Ability to manage regulatory submissions

Nice-to-have

  • Experience with Health Authorities interactions
  • Ability to formulate regulatory strategy
  • Promotes an inclusive culture

Key Requirements

  • BSc or advanced scientific degree preferred
  • Fluency in English

Work Rights

Not specified

Tailored Resume

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