/ http://www.slideshare.net/images/logo.gif / ºÝºÝߣShare feed for ºÝºÝߣshows by User: DuarteMartins3 https://cdn.slidesharecdn.com/profile-photo-DuarteMartins3-48x48.jpg?cb=1461323027 I develop purification process for vaccines and gene therapy vectors to be transferred to GMP manufacturing as part of our CMO activity. My responsibilities include: • Review technology transfer documents and conduct risk assessment prior to process implementation; • Definition of process development plans for purification accordingly with the risk-assessment evaluation and the Quality by Design (QbD) initiative; • Definition of the relevant product analytical characterization and process characterization; • Writing of SOPs and batch production reports; • Hands-on operation of purification equipments for microfiltration, ultrafiltration and chromatography (ÄKTA ... http://www.researchgate.net/profile/Duarte_Martins/