Production Process Expert (temporary)

Novartis Italia; Saluggia; In loco; EUR 40.000 - 55.000; Tempo pieno

Descrizione del lavoro

A leading pharmaceutical company in Saluggia, Italy is seeking a Production Process Expert to optimize and support production processes while ensuring compliance with GMP standards. The role requires a scientific degree and experience in a GMP manufacturing environment. Fluent Italian and good English skills are essential. This is a temporary contract for 1 year, offering a collaborative work environment focused on innovative science.

Competenze

• Experience in a GMP manufacturing environment is essential.
• Fluency in Italian and a good knowledge of English are required.

Mansioni

• Manage Production Process optimization projects.
• Provide technical support for manufacturing processes.
• Support the development of new products.

Conoscenze

Process optimization

GMP knowledge

Problem-solving

Data Integrity

Collaboration

Formazione

Scientific degree

Descrizione del lavoro

Summary

The Production Process Expert is part of the Manufacturing Team and provide to support the production process regarding investigations and process monitoring to ensure execution of process on time and in compliance with applicable GMPs, SOPs, guidelines.

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? https://www.novartis.com/about/strategy/people-and-culture

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