Ph3Job Description Summary /h3 pLocation: Ivrea, Italy #onsite /p pRole Purpose: Act 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). /p pDevelop, 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). /p h3Job Description /h3 pMajor accountabilities: /p ul liManage inter functional project plan and budget using the Project Planning tool or System /li liIdentify issues and potential bottlenecks within projects and proposes options /li liContribute 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. /li liParticipate 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. /li liIdentify strategic external partners for the activation of research collaboration agreement to develop new production technologies/ access to innovative isotopes. /li liImplements strategic policies when selecting methods, techniques, and evaluation criteria for obtaining results. /li liEstablishes and assures adherence to budgets, schedules, work plans, and performance requirements. /li liRepresents 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). /li liReporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt /li /ul pMinimum Requirements: /p ul liBSc. in Chemical Engineering, Pharmaceutical Technology, or equivalent scientific degree. /li liDesirable MSc., PhD or equivalent experience. /li liDesirable degree in Radiochemistry and strong scientific knowledge in nuclear medicine /li liSuccessfully demonstrated several years (minimum of 5 years) of directly related experience in a scientific area or Ph.D. or equivalent /li liProven Project Leadership in all project phases /li liProven process understanding (Pharma, GMP, Validation and Regulatory aspects). /li liSound experience of data handling and applied statistics is a must. /li liStrong understanding of risk assessment and risk management fundamentals/tools /li liQuality-oriented with attention to detail /li liExcellent verbal and written communication skills /li liExcellent problem solving and decision-making skills /li liDefining and implementing productivity improvement measures. /li liItalian language needed as a site language /li /ul pCommitment 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 pbSkills Desired /b /p /p #J-18808-Ljbffr