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You will oversee a team responsible for managing the end-to-end regulatory artwork process for pharmaceutical and non-pharmaceutical products across Europe. In addition to your leadership responsibilities, you’ll remain actively involved in daily
Act as the representative of European regulatory team at the global regulatory team (GRT) for the designated projects needing diagnostics, and may also be required to represent diagnostic strategies to global cross-functional teams for specific topics;
Аctively support from CMC-perspective the whole evaluation and execution of projects (such as site transfers, sourcing changes and volume transfers) and liaise with other team members to make sure that timelines are met. Plan Team activities