Isotope Project Lead (Associate Director S&T)

Novartis Pharma Schweiz · Ivrea, Piemonte, Italia · · 50€ - 70€


Descrizione dell'offerta

Major Accountabilities

  • Manage inter functional project plan and budget using the Project Planning tool or System
  • Identify issues and potential bottlenecks within projects and proposes options
  • Contribute 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.
  • Participate 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.
  • Identify strategic external partners for the activation of research collaboration agreement to develop new production technologies/ access to innovative isotopes.
  • Implements strategic policies when selecting methods, techniques, and evaluation criteria for obtaining results.
  • Establishes and assures adherence to budgets, schedules, work plans, and performance requirements.
  • Represents 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).
  • Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt

Minimum Requirements

  • BSc. in Chemical Engineering, Pharmaceutical Technology, or equivalent scientific degree.
  • Desirable MSc., PhD or equivalent experience.
  • Desirable degree in Radiochemistry and strong scientific knowledge in nuclear medicine
  • Successfully demonstrated several years (minimum of 5 years) of directly related experience in a scientific area or Ph.D. or equivalent
  • Proven Project Leadership in all project phases
  • Proven process understanding (Pharma, GMP, Validation and Regulatory aspects).
  • Sound experience of data handling and applied statistics is a must.
  • Strong understanding of risk assessment and risk management fundamentals/tools
  • Quality-oriented with attention to detail
  • Excellent verbal and written communication skills
  • Excellent problem solving and decision-making skills
  • Defining and implementing productivity improvement measures.
  • Italian language needed as a site language

Commitment 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.

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Candidatura e Ritorno (in fondo)