Associate Director, Global Regulatory Strategic

vor 8 Stunden

Zurich, Schweiz Takeda Pharmaceutical Vollzeit

Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine?Join us as a **Associate Director, Global Regulatory Strategic Sourcing** in Zurich, Switzerland. **Here, you will be a vital contributor to our inspiring, bold mission.**

**OBJECTIVES**
- Providing support and assisting the Head of Global Regulatory Strategic Sourcing/ Director of Global Regulatory Strategic Sourcing with leadership and executing oversight for all supplier management activities within Europe in support of our flexible capacity model (functional service provider, outsourcing) across the Global Regulatory Affairs Organization
- Leverage relationships with our suppliers to support business needs, support execution on business plans for the performance of these groups. He/she will assist in ensuring operational performance across the Regulatory organization and assist with resolution of less complex operational issues and will work with the Head of Global Regulatory Strategic Sourcing/Director of Global Regulatory Strategic Sourcing to resolve highly complex or unusual operational issues.
- Providing support in establishing an integrated ecosystem of business process and technical innovation
- This role has will support oversight for external capacity within Europe

**ACCOUNTABILITIES**:
The Associate Director, Global Regulatory Strategic Sourcing will demonstrate Takeda leadership behaviors to accomplish the following responsibilities that include but are not limited to:
You are a great fit for this opportunity if you are engaged and energized by:

- Support an outsourcing vision to achieve current and future business objectives and to continuously optimize outsourcing for Company’s Global Regulatory Affairs (GRA) Organization
- Support the operational, management governance, and executive relationships between our Company and external partners within Europe to deliver on objectives and to support the partner's ability to execute on our sourced scope of work
- Manage processes and connections between the external partners within Europe and the various stakeholders across GRA.
- Work with Head of Global Regulatory Strategic Sourcing/ Director of Global Regulatory Strategic Sourcing to collaborate with internal teams and external parties to ensure best possible delivery of sourced activities according to established KPIs.
- Provide regular feedback to management on the performance of partners, and support in ensuring deliverables are met and performance issues are identified, managed, and rectified, and providing regular feedback to partner management and internal teams on performance issues.
- Participate with Head of Global Regulatory Strategic Sourcing/ Director of Global Regulatory Strategic Sourcing to envision future processes and technologies and willingness to explore approaches used by other industries beyond pharma/life sciences to deliver tangible process improvements that enable a more digitally enabled GRA.
- Work with procurement, Finance, IT and Functional Area experts to support the conduct of due diligence evaluations and selection of external partner organizations.
- Support and assist in establishing an industry-leading approach to joint process improvement and innovation ecosystem across our Company and partner companies for externalized work.
- Manage and continuously develop a team of our Company professionals that deliver industry leading supplier management.

**We would be thrilled if you brought the following with you**:

- At least 3 years of biopharmaceutical experience with at least 1 years in R&D functions such as Pharmacovigilance, Regulatory Affairs, Clinical Research, etc. (Regulatory Expereince preferred).
- Bachelor of Science Degree in Technical Discipline such as Life Sciences or Health Care Professions (Engineering, Biology, Chemistry, Nursing, Pharmacy) or related discipline. Master of Business Administration degree preferred.
- Demonstrated experience working in a drug development outsourced model, either on the outsourcer or client side with an ability to translate learnings to a regulatory outsourcing model
- Experience with supporting successful delivery of projects (pipeline, business improvement, and/or change management projects) as well as Demonstrated experience driving change / transformation projects
- Understanding of relationship management with demonstrated experience in partnering in large scale situations
- Innovative thinking in order to drive insights into operations and change management and support strategic sourcing decisions.
- Must have proven track record to be able to think critically, independently and problem solve
- Must have high level of motivation, drive, and demonstration of Takeda’s leadership values
- Excellent written and verbal communication skills
- Top notch interpersonal skills in difficult situations
- Ability to work seamlessly with all levels of personnel

**WHAT TAKEDA CAN OFFER YOU**

At Takeda, we

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