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Lead technology transfers and regulatory submissions while managing multiple programs in line with CMC objectives and timelines. Apply Best Product at Pivotal and Speed to the Clinic principles, prioritize resources across competing programs, and ensure
Provide QA support and expertise to iPSC cell culture, cell banking, cell differentiation in bioreactor and aseptic manufacturing activities; Maintain a strong QA presence on the shop floor and promote a proactive, right-first-time quality culture;
Design and execution of agreed work plans for the production and characterization of membrane proteins; Responsible for supporting multiple projects and may be asked to direct internal resources to achieve agreed goals
Utilize and establish advanced in vitro and in vivo models of ocular disease, and leverage available patient sample datasets to identify, validate, and characterize novel therapeutic drug targets; Independently lead and manage drug discovery projects from
You will lead a new global organization consisting of groups based across multiple sites and countries and report directly to the Global Head of BioAnalytics, CMC Development. You will be responsible for analytical characterization of therapies across all