for New Product OpportunitiesUtilise insights from the product development pathway and global biopharmaceutical trends to guide R&D policy, support preparation of regulator packages and identify new
external collaborators to make recommendations on study design, execution and data analysis. The Role Oversee and provide support in statistical methodology for experimental design, data analysis
Fulltime / permanent/ non-tariff Do you want to work in a global team and support regulatory strategies of plasma-derived products in all phases of development, from preclinical to post approval phase
Für unseren Value Stream – Site Logistics Support in Marburg suchen wir aktuell eine/n Teamleiter/in Support (m/w/x) R-249579 Vollzeit / unbefristet Aufgaben Personaleinsatzplanung
Für unseren Value Stream – Site Logistics Support in Marburg suchen wir aktuell eine/n Teamleiter/in Support (m/w/x) R-249578 Vollzeit / unbefristet Aufgaben Personaleinsatzplanung
designated cluster. This position provides expert input on pharmacovigilance-related matters and develops strategy for the assigned cluster, ensuring PV processes are completed seamlessly in support of the
accumulated overtime for sabbaticals, special leave, or an early start into retirement (Marburg)Family services such as psychological support, legal advice, family care services and more for you and your direct
, Sartocheck-Testgeräte) gemäß Anforderungen aus der ProduktionInstallation von neuer Hard- und SoftwareSchulung der Benutzer im MESNeuanlage und Pflege von User Accounts im MESSecond Level Support für die MES
great job opportunity will be located in Marburg and reports directly into the Associate Director Services and Consultancy Sourcing in Australia. The Opportunity In this position you will support
and develop a team comprised of process engineers and or scientistLead technical workstreams of complex projects at the site level or at the global level to support process changes, process improvements
, Research & Development Quality Assurance (R&DQA) and Clinical.Maintains up-to-date understanding of safety profiles of registered and investigational products. Supports and collaborates with cross-functional
training to support study execution for clinical sites and patients (e.g. Investigational Medicinal Product (IMP) Manuals, product preparation and administration videos). Trains external stakeholders (i.e