Riehen, Basel, Switzerland
Overseeing all manufacturing processes at 3rd party manufacturers and vendors for API, Drug Product and Finished Products. Since 2019 scientific workstream lead for all Nitrosamine Risk Assessments.
Manufacturing Science and Technology provides product and manufacuring process understanding in Technical Operations and ensures that products and processes are in a constant state of control.
Product Allocation is the process of determining and obtaining a product manufacturing site for any final dosage form for launch or routine supply.
Drug Supply Management is a global function within Pharma Development and is in charge of establishing & managing the supply chain for investigational medicinal products from API over drug product including packaged clinical supplies. Additionally medication supplies for all clinical trials worldwide (Phase I-IV) are to be designed, packaged and supplied including the medication management throughout the conduct of the clinical trial.
GMP manufacturing and scale up of oral, sterile and semisolid dosage forms for use in clinical studies including management of 3 GMP pilot plants.
Build up and leadership of Clinical Manufacturing Group within Pharmaceutical Development for production of clinical supplies according to GMP.
Development of Formulations and processes for oral solid dosage forms, sterile dosage forms and dry powder inhalation dosage forms