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In this role, you’ll provide global scientific and technical leadership, contribute to innovation strategies, and act as a thought leader - both within Lonza and the wider biopharmaceutical industry. Guide development of mammalian USP/DSP processes for
Responsible for all tasks and resources including cross functional co-ordination required to complete relevant QC microbiology activities within regulated environment in the required timeframe. Management of QC Microbiology team to carry out tasks.
Lead the full lifecycle of complex programs from contract signature to delivery. Act as the single point of contact for customers and advocate for their needs on-site. Ensure delivery on time, within budget, and to the highest quality standards.
Mit dem Themenfeld der neuartigen Therapien und den regulatorischen Anforderungen an die Herstellung und Prüfung entsprechender Arzneimittel sind Sie vertraut; Zudem haben Sie bereits Erfahrung mit der Akquise und/oder Umsetzung von GMP-Beratungs- und