EU Regulatory Lead, Neuroscience — Associate Director

CHE - 8036 Takeda Pharmaceuticals International AG; Glattbrugg; Vor Ort; CHF 159.000 - 219.000; Vollzeit

Zusammenfassung

Takeda Pharmaceuticals International AG in Zurich seeks an Associate Director, EU Regulatory Lead Neuroscience to define and lead regional regulatory strategies for neuroscience assets, supporting development, registration, patient access and lifecycle management. You will collaborate with global and regional teams to navigate EU regulatory requirements, drive high-quality submissions and lead interactions with Health Authorities.

Travel international as required.

Qualifikationen

• Requires minimum of 8 years in drug regulatory affairs, with significant EU experience.
• Strong knowledge of EU regulatory requirements across development and lifecycle.
• Proven ability to lead regional regulatory strategies and submissions.

Aufgaben

• Define, develop and execute progressive EU regulatory strategies for neuroscience assets.
• Lead regional regulatory submissions and ensure timely approvals.
• Provide regulatory guidance to global, regional and cross-functional teams.
• Lead or support interactions with Health Authorities and regulatory meetings.

Kenntnisse

EU regulatory knowledge

Regulatory submissions

Stakeholder management

English fluency

Travel readiness

Ausbildung

Bachelor's degree

Advanced scientific degree preferred

Jobbeschreibung

Takeda Pharmaceuticals International AG in Zurich seeks an Associate Director, EU Regulatory Lead Neuroscience to define and lead regional regulatory strategies for neuroscience assets, supporting development, registration, patient access and lifecycle management. You will collaborate with global and regional teams to navigate EU regulatory requirements, drive high-quality submissions and lead interactions with Health Authorities.

Travel international as required.