You will work in Tübingen, Munich or remote (Germany) and act as the key regulatory interface for CMC topics, working closely with Quality, Global Drug Supply and external manufacturing partners to ensure robust, pragmatic, and compliant CMC strategies. * Proactively identify CMC regulatory risks (e.g., comparability, specification changes, site transfers) and propose pragmatic mitigation approaches while ensuring compliance with regulatory requirements. * Master or PhD in natural sciences (e.g., Biology, Chemistry or Pharmacy). * Proven track record preparing and contributing to EU Health Authority interactions (e.g., Scientific Advice). We believe in supporting our and social skills: We enable them to join conferences and trainings as well as to enjoy our Immatics benefits – e.g., job bike, job ticket, Health Programs, childcare benefits, relocation allowance, Company summer and winter events.
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