RUEIL MALMAISON 2010 - maintenant• Validation of a manufacturing process in order to get Health authorities approval to produce a monoclonal antibody. Organization of process validation studies at manufacturing scale. Writing of process validation reports (Cell culture & Purification parts). Working Words INC training.
• Handling of process deviations and “Out Of Expectation / Specification” (AQWA software). Implementation of correctives and preventives actions.
• Support to the manufacturing production according to GMPs for the DownStream Processing. Establishment of control charts to monitor the manufacturing process.
• Back-up of the unit expert for the DownStream Processing.
Formations
Université De Strasbourg (Illkirch)
Illkirch2009 - 2010Biotechnologies
Master Biotechnologies et Innovations Thérapeutiques
Ecole Supérieure De Biotechnologies De Strasbourg (Strasbourg)
Strasbourg2007 - 2010Biotechnologies - Ingénieur en Biotechnologies
