摘要
About the Role
Major accountabilities:
- Management of Production Process optimization projects.
- Provide technical support with regard to manufacturing processes, investigations, optimization and problem solving.
- Support to the TRD (Theragnostic Research and Development) department in the development of new products.
- Timely handling of Production Department investigations and deviations.
- Manage Investigations and Troubleshooting in Production Department and ensures corrective and preventive actions are implemented timely.
- Support in the development and implementation of Production Department strategies.
- Ensure Data Integrity in Production Department.
- Support Production Department process optimization and the introduction of new the technologies for the continuous improvement, acting as Subject Matter Expert of products and processes
- Review documentation, Master Batch Records, SOP and other procedure concerning production department. Ensure Timely update of SOPs and Change.
- Collaborate with the Production Manager with the aim of ensuring the achievement of production objectives consistent with the GMP (quantity, mix, costs) through the verification of the correct application of the planning of the activities.
Essential requirements:
- Scientific degree.
- Previous experience in a GMP manufacturing environment.
- Fluent in Italian. Good knowledge of English.
We offer a temporary contract of 1 year.
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? http://www.novartis.com/about/strategy/people-and-culture
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Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
