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By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice an…
Skills: EU Regulatory Strategy, Drug Regulatory Affairs, Health Authority Interactions, Lifecycle Management, Regulatory Submissions
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice an…
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$159k–$219k/yr
Full-time
bachelor degree, postgraduate degree
Posted 21d ago
~40 hrs/week
Responsibilities
Define and lead regional regulatory strategies for neuroscience assets to support product development, registration, and patient access in the EU. Lead high-quality regulatory submissions and manage interactions with European and national Health Authorities.
Requirements
Requires a bachelor's degree in a scientific discipline and at least 8 years of experience in drug regulatory affairs, specifically within the EU region. Must possess strong knowledge of EU regulatory requirements and proven experience leading interactions with Health Authorities.
Full job description
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description
About the role
As the Associate Director, EU Regulatory Lead Neuroscience, you will define and lead regional regulatory strategies for assigned neuroscience assets, supporting successful product development, registration, patient access and lifecycle management. You will work closely with global and regional cross-functional teams to navigate the evolving European regulatory environment, drive high-quality submissions and lead interactions with Health Authorities.
How you will contribute
Define, develop and execute progressive EU regulatory strategies for assigned neuroscience assets across development and lifecycle management.
Lead and manage regional regulatory submissions, ensuring high-quality execution and timely approvals.
Provide strategic and tactical regulatory guidance to global, regional and cross-functional project teams.
Lead Submission Working Groups and represent the EU region on global regulatory and project teams.
Lead or support interactions with European and national Health Authorities, including preparation for regulatory meetings and effective communication of outcomes.
Assess emerging regulatory trends, guidance and requirements and translate their potential impact into proactive regulatory strategies.
Provide regulatory expertise across drug development, registration, post-marketing commitments and lifecycle management activities.
May support value and access team in interactions with Health Technology Assessment bodies.
Build strong relationships with local and global Regulatory Affairs teams, cross-functional partners, external experts and regulatory authorities.
What you bring to Takeda
Bachelor’s degree in a scientific discipline required; advanced scientific degree highly preferred.
Minimum 8 years of experience in drug regulatory affairs, preferably with significant experience in the EU region.
Strong knowledge of EU regulatory requirements and guidance across all phases of drug development and ability to orient project teams; an understanding of basic regulatory requirements in other regions globally (US, Emerging markets) is a plus.
Proven ability to develop and execute regional regulatory strategies supporting competitive and timely product approvals.
Experience with investigational regulatory submissions, such as clinical trial applications, scientific advice briefing books, orphan designations, paediatric plans, or initial Marketing Authorisation Applications.
Experience participating in or leading interactions with Health Authorities.
Strong strategic thinking with the ability to assess regulatory opportunities, risks and mitigation strategies.
Excellent communication, influencing and stakeholder management skills across global and cross-functional teams. Can speak up and is perceived as a natural, assertive authority whom peers trust for their advice.
Fluent in English, able to work independently in a complex environment and willing to travel internationally as required.
Locations
Zurich, Switzerland
Base Salary Range:
CHF159,300.00 - CHF219,010.00
For information about our benefits, please click here.
We strive to transform lives. While the science we advance is constantly evolving, our core purpose is enduring. For more than two centuries, our values have guided us to do what’s right for patients and for society.
We know that changing lives requires us to do things differently. We start by listening to and addressing what really matters to patients, the people who love them, and those in the healthcare system who provide care. And that’s what inspires us all to be bold, push boundaries and set new standards that open up greater opportunities.
Read our community guidelines: https://takeda.info/communityguidelines
Offices: Tokyo, JP · 1 Takeda Parkway, Deerfield, Illinois 60015, US · 40 Landsdowne St, Cambridge, Massachusetts 02139, US · Avenida das Nações Unidas, 14.401, Torre Jequitibá - 10°, 11° e 12° andares, São Paulo, 04794-000, BR · 43 Old Oak Rd, Bellville, Western Cape 7550, ZA
How many Healthcare jobs are open in Zurich, Switzerland right now?
There are currently 308 open healthcare positions in Zurich, Switzerland listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Healthcare roles in Zurich, Switzerland?
Companies currently hiring include Mediclinic Middle East, Takeda, Medbase Gruppe, Schulthess Klinik, Clinique Valmont, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Healthcare jobs in Zurich, Switzerland?
Yes — 80 of the 308 open healthcare positions offer remote or hybrid work (14 remote, 66 hybrid).
How do I apply for Healthcare jobs in Zurich, Switzerland?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.