
Pharma · Schweiz
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Fresenius KabiPharmaLeitung Customer Service & Insurance Management (m/w/d), 100%
Job Summary Für unser Customer Service & Insurance Management Team suchen wir per Januar 2027 oder nach Vereinbarung eine engagierte Persönlichkeit als Leitung Customer…
NEU1 day ago CH
Fresenius KabiPharmaRegulatory Affairs Manager (m/f/d)
Job Summary Position Location: SPAIN Purpose: The Regulatory Affairs (RA) Manager supports the development and execution of global regulatory strategies for assigned biosimilar…
7 days ago CH
Fresenius KabiPharmaDirector Medical Device Program Lead
Job Summary In this position, you will be the back-up of the head of the device team.
8 days ago CH
Fresenius KabiPharmaVice President Head of Medical Affairs
Job Summary Responsibilities / Duties: • Define and lead the evolved Medical Affairs vision, operating model and transformation roadmap, shifting the function from primarily…
9 days ago CH
Fresenius KabiPharmaDirector Business Development - Biopharma (m/f/d)
Job Summary This position can be based in Switzerland (Eysins), Germany (Bad Homburg) or Spain (Madrid).
13 days ago CH
Fresenius KabiPharmaInternship Marketing
Job Summary In unserem Marketingteam bieten wir per 1. Januar 2027 für 12 Monate eine spannende und vielseitige Praktikumsstelle Marketing: Unterstützung für innovative Projekte…
21 days ago CH
Fresenius KabiPharmaSenior Manager European Patent Attorney (m/f/d)
Job Summary Location: Eysins, Switzerland, or remote from anywhere in Switzerland. Functional Goal: Support the business on all patent related questions to enable product launches.
CH
Fresenius KabiPharmaSenior Manager Clinical Operations (m/f/d)
Job Summary Location: Spain and Hungary Functional Goal: Responsible for the strategic and tactical operational planning and execution of R&D sponsored clinical programs for…
CH
Fresenius KabiPharmaSenior Manager Regulatory Affairs Lead
Job Summary Main Tasks: Key accountability: Provides global regulatory leadership regarding biosimilar development and management of submission related documents, regulatory data…
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