Strategic Sourcing Operations Director
vor 4 Wochen
Job Summary
We are seeking a highly skilled Regulatory Affairs CMC Device and Drug-Device Combinations Lead to join our team at Takeda. This role will be responsible for end-to-end management of device and drug-device combination work outsourced by the Global Regulatory Affairs CMC Device and Drug-Device Combinations to external partners.
Key Responsibilities
- Utilize regulatory strategy and/or operational expertise to shape global regulatory best practices, drive internal consistency, and influence effective change management.
- Build and manage strong working relationships through active partnering with key internal and external stakeholders.
- Proactively identify combination product and device-related regulatory risks, ensuring timely communication with line management.
- Support assigned work on drug-device combination aspects of regulatory submissions in collaboration with sourcing partners.
- Develop and maintain constructive relations with key internal and external colleagues.
Requirements
- BS/BA Degree in a Scientific, Pharmaceutical, or Engineering Discipline.
- 8+ years of pharmaceutical Regulatory CMC and Medical Device experience, including experience as a regulatory representative for drug-device combination products.
- Experience working on cross-functional submission teams.
- Solid understanding and proven ability to provide strategy on regulatory requirements relevant to global drug-device combination product development, registration, and post-market support.
- Experience supporting interactions with EMA, Notified Bodies, and other global health authorities specifically related to Combination Products and Device submissions is strongly preferred.
Travel Requirements
- Willingness to travel to various meetings or events, including overnight trips. Some international travel may be required.
Location
Zurich, Switzerland
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
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