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Your responsibilities
We are seeking an enthusiastic and highly professional expert to fill the position of the Founding Director for establishing the Zurich Hub for Drug and Device Development (ZH3D). ZH3D will accelerate the development of innovative drugs and medical devices at the UZH and in the Zurich area by coordinating existing GxP platforms and providing innovative GxP-related services and education. Together with the University Hospital Zurich (USZ), the UZH offers already established, Swissmedic accredited platforms for GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice), and GCP (Good Clinical Practice).
The Director will be responsible for the establishment, management, and development of the ZH3D, which shall be expanded into a nationwide research structure. His/her tasks will include:
1. The establishment of a coordinated and centralized QM, ISO13485 support for in vitro diagnostics (IVD) and medical devices (MDR) development.
2. The establishment of a GxP academy as a structured continuing education program, licensing models and negotiations with investors and sponsors.
3. S/he will recruit and coordinate a high-performing team of experts and establish and maintain strong relationships with key stakeholders, including universities, hospitals, pharmaceutical companies, and regulatory agencies.
4. S/he will manage the Hub's budget.
5. Finally, s/he will be the first point of contact for the ZH3D, promoting its mission to the scientific community and the public.
As the Founding Director, we seek a highly motivated and experienced leader with a strong interest in research from bench-to-bedside and drug and device development. S/he will be responsible for building the institute from the ground up, establishing a strong team, and implementing the strategic vision to position ZH3D as a primary center of excellence for drug and device development excellence at the UZH and in Switzerland into action.
Your profile
* A proven track record of managing research-oriented units in a large organization and previous participation in interdisciplinary projects.
* Hands-on experience in drug and/or medical device development with a strong understanding of the regulatory requirements for GMP, GCP, GLP, and IVD in Switzerland.
* Excellent communication, interpersonal, and negotiation skills.
* A broad national and international network within the scientific and regulatory communities.
* Fluency in English and German.
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