Isotope Project Lead (Associate Director S&T)
Pubblicato il 28-10-2026 - Novartis in Ivrea
h3Job Description Summary /h3pLocation: Ivrea, Italy #onsite /ph3Role Purpose: /h3pAct as Isotope Project Lead (IPL) by providing the specialist knowledge and expertise as Subject Matter Expert (SME) of radioisotope production and purification with particular focus on assessing, developing, and optimizing new technologies that support RLT products Life Cycle Management (LCM). /ppDevelop, optimize and transfer radioisotopes production and purification/separation processes. This is done in close collaboration with the relevant development centers, and Contract Manufacturing Organizations (CMOs). /ph3Job Description /h3h3Major accountabilities: /h3ulliManage inter functional project plan and budget using the Project Planning tool or System /liliIdentify issues and potential bottlenecks within projects and proposes options /liliContribute to the Radioisotope TRD-related activities. Ensure constant technological survey on the field of radioisotopes production. Apply scientific/technical expertise to identify new programs of interest for the company and support their development from early evaluation up late phase supply. /liliParticipate to development programs and activities around isotopes in adherence with global Isotope strategy and objectives within agreed timelines and budget, timely report key advancements and challenges. /liliIdentify strategic external partners for the activation of research collaboration agreement to develop new production technologies/ access to innovative isotopes. /liliImplements strategic policies when selecting methods, techniques, and evaluation criteria for obtaining results.
/liliEstablishes and assures adherence to budgets, schedules, work plans, and performance requirements. /liliRepresents area as core member in the Global Project Teams for defining global scientific strategy for development up to submission and approval in major markets of assigned product(s). /liliReporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt /li /ulh3Minimum Requirements: /h3ulliBSc. in Chemical Engineering, Pharmaceutical Technology, or equivalent scientific degree. /liliDesirable MSc., PhD or equivalent experience. /liliDesirable degree in Radiochemistry and strong scientific knowledge in nuclear medicine /liliSuccessfully demonstrated several years (minimum of 5 years) of directly related experience in a scientific area or Ph.D. or equivalent /liliProven Project Leadership in all project phases /liliProven process understanding (Pharma, GMP, Validation and Regulatory aspects). /liliSound experience of data handling and applied statistics is a must. /liliStrong understanding of risk assessment and risk management fundamentals/tools /liliQuality-oriented with attention to detail /liliExcellent verbal and written communication skills /liliExcellent problem solving and decision-making skills /liliDefining and implementing productivity improvement measures. /liliItalian language needed as a site language /li /ulpCommitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. /p #J-18808-Ljbffr