Project Manager in Radiopharmaceutical Production 80-100% (m/f/d)
Auf einen Blick
- Veröffentlicht:26 März 2025
- Pensum:80 – 100%
- Vertragsart:Festanstellung
- Sprache:Deutsch (Fliessend), Englisch (Fliessend)
- Arbeitsort:Zürich
The Radiopharmacy of the University Hospital of Zürich is the pioneer and most important manufacturer of PET radiopharmaceuticals in Switzerland, offering a wide variety of innovative products in the fields of oncology, neurology, and cardiology. With over 30 years of experience in the field, a state-of-the-art GMP-compliant radiopharmacy and a new production facility, expected to be operational in the coming months, we are looking for a hands-on and highly committed project manager.
The University Hospital of Zurich is one of the largest hospitals in Switzerland. Our more than 8, 600 employees and around 700 trainees work every day for the well-being of our patients.
The University Hospital of Zurich is one of the largest hospitals in Switzerland. Our more than 8, 600 employees and around 700 trainees work every day for the well-being of our patients.
By agreement
Your main tasks
- You report directly to the deputy head of the radiopharmacy and to the Qualified Person regarding GMP matters
- Your main responsibility will be to lead and actively participate in the update/transfer of operating site projects, as well as in the implementation of new ones. This includes planning, coordinating and supervising the required activities for the transfer/update/implementation of projects, related to the manufacturing of diagnostic radiopharmaceuticals
- Creation of project documents: transfer plans, validation plans and reports, operating procedures, etc. You will receive support from the production, quality control, and quality assurance teams
- Direct participation, as required, in the activities and experiments related to project transfer/implementation (qualification/validation activities)
- Since we are a small team (25 employees), you will also be expected to support the production and quality control teams, solving operational issues as they arise
Your profile
- Master degree or equivalent formation in chemistry, pharmacy or related fields
- A minimum of 2-3 years practical experience in project development in a GMP regulated laboratory, with emphasis in analytical method development
- Knowledge of national regulations regarding medicinal products is a big asset
- Interdisciplinary approach: you should be able to maintain the project overview and coordinate between the production, quality control and quality assurance teams
- Independent planning and working, as well as a proactive, pragmatic attitude
- Hands-on person and a good team player, willing to participate in all activities related to the project
- Solid computer and analytical skills
- Fluent in German and English
Our offer
We offer you a varied role in a progressive work environment, characterized by high quality, independence, flexibility, and responsibility. Within the scope of your work, you will have considerable creative freedom and the opportunity to actively contribute your knowledge and skills. Your are part of a motivated and dedicated team, which will support you in all aspects. Benefit from excellent employment conditions, flexible working models, and a wide range of internal training opportunities.
Universitätsspital Zürich
8091 Züric
8091 Züric
