RLT Analytical Product Project Leader (m / f / d) Job ID : REQ-10015150 Location : Ivrea, Italy Summary Role Purpose : Define, lead, and manage the analytical project strategy, including the overall analytical control strategy for Drug Substance(s) and radiopharmaceutical parenteral Drug Product(s), in line with the overall CMC project development plan. Ensure high-quality analytical submission documents. Support and mentor analytical team members, contributing to the overall Technical Research and Development strategies and goals. Role Responsibilities : Define and develop a science- and quality-driven analytical project strategy, including contingency plans and risk evaluations for RLT DS and RLT DP. Ensure transparent communication with management and relevant project team members. Be a core member of the TRD sub-team representing RLT Analytical Science; co-own technical development with DSPL and RLT DPPL, and contribute to the technical development plan. Lead and coordinate analytical activities (method development and validation, stability, release, reference nomination, transfer) across all analytical sites and partnering functions. Drive testing strategy and specifications setting for RLT DS / DP; represent RLT Analytical Science in peer reviews, governance boards, audits. Support resource planning, budget adherence, and monitor monthly resource needs. Create and document high-quality control strategies with partnering functions, including risk assessments. Handover analytical documents to internal and external partners; lead interactions across sites and functions; support outsourcing projects and QA agreements. Minimum Requirements : PhD in chemistry, pharmaceutical technology, or equivalent with at least 5 years of industry experience in analytical chemistry, radiochemistry, or quality control, including project management. Fluent in English (oral and written); knowledge of site language is desirable. Proficiency in GMP and understanding of regulatory and quality expectations in radiopharmaceuticals. Experience in writing CMC documents for regulatory submissions and responding to health authority questions. Experience with outsourcing and coordinating CRO/CMO work, including technical agreements. Awareness of safe handling of chemicals and potentially hazardous materials. Why Advanced Accelerator Applications? Our mission is to transform lives through radioligand therapy to fight cancer. We foster innovation, diversity, and an inclusive environment, driven by integrity, curiosity, and collaboration. Join us to make a difference in medical science and patient care. Imagine what you could do at Novartis! We are committed to building an inclusive, diverse work environment that reflects the communities we serve. J-18808-Ljbffr J-18808-Ljbffr