05.05.2025 | Pełny etat | Wysokie Mazowieckie | Bayer Sp. z o.o.Product management and a broad knowledge in the area of consulting You have a profound knowledge of business processes in R&D/ Regulatory Affairs GxP expertise is required Veeva RIM expertise is required, Veeva certification (Platform, eTMF, RIM etc.) preferred You have proven leadership, intercultural
Zobacz później29.04.2025 | Pełny etat | Warszawa | Randstad Polska Sp. z o.o.Step into a pivotal role as Manager, Regulatory Affairs and contribute to the global development and lifecycle management of groundbreaking pharmaceutical products. As a key member of team, you will lead the development and execution of global CMC regulatory strategies, ensure compliance
Zobacz później01.05.2025 | Pełny etat | Warszawa | PrimeVigilanceWe are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider established in 2008. We have achieved consistent global growth, with staff across Europe, North America, and Asia, providing services in Medical Information, Pharmacovigilance, Regulatory Affairs
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