This position has the overall responsibility for the global manufacture of Attovia’s novel biologics platform molecules, from the later stages of discovery trough preclinical and clinical development, up to the commercial and life cycle phase of novel therapeutics.
This individual is accountable for delivering GMP manufacturing of Attovia’s pipeline molecules and to support regulatory filings across all global healthcare regions. In addition to formulation, process, and analytical development, the position oversees multi-disciplinary international teams supporting Quality oversight, supply chain, CMO/CRO strategy and execution, and manufacturing technology implementation and transfer.