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Product Development, 2nd Sourcing und International Market Access\nDas bringen Sie mit\nNaturwissenschaftliches Studium oder vergleichbare Qualifikation\nMehrjährige Erfahrung im GMP-regulierten Pharmaumfeld, idealerweise als GMP-Lead Auditor\nAlternativ fundierte Erfahrung in der Herstellung von Wirkstoffen, aseptischen oder biotechnologischen Arzneimitteln bzw. in Qualifizierung und Validierung\nSehr gute Kenntnisse der GMP-Regularien sowie Erfahrung mit internationalen Behörden wünschenswert\nHohe Reisebereitschaft (ca. 50 % national und international)\nVerhandlungssichere Deutsch- und Englischkenntnisse\nAusgeprägte Kommunikationsstärke, Durchsetzungsvermögen sowie ein souveränes Auftreten\nDas bieten wir Ihnen\nFlexibel und eigenverantwortlich: In vielen Unternehmensbereichen können sich unsere Mitarbeitenden ihre Arbeitszeiten frei einteilen - und bis zu 60 % remote arbeiten\nWir bieten 30 Urlaubstage im Jahr und Urlaubsgeld\nBesondere Leistung verdient besondere Wertschätzung. 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