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Production supervisor - temporary contract

Ivrea
Novartis
Pubblicato il 8 gennaio
Descrizione

Summary: The Production Supervisor supports the Production Manager to ensure the running of a production shift team such that the manufacturing program is achieved efficiently within the framework of regulatory compliance and operating within high standards of GMP, HSE, environmental protection and good working practices. About the Role: Major accountabilities: In addition to technicians' missions: - To ensure that the raw materials used for the manufacturing process are always available in the right amount and properly stored according their status - Support the production Manager to write down and to validate the Standard Operating Procedures and Work Instructions relating to production operations and to ensure their strict implementation. - Be the Deputy of Production Manager in managing, coordinating and approving the execution of the production activities for the batch release when Prod Manager is not on site Support Production Manager to ensure proper qualification and maintenance of the manufacturing department, premises and equipment. - Support Production Manager to ensure proper validation of relevant processes. - To ensure, in collaboration with Production Manager, appropriate initial and continuing training of the manufacturing department personnel. - Manage the presence, shifts and performances of the Production Technicians when Production Manager is not on site - To manage the re-planification in case of failure to mitigate the impact for the patient in collaboration with QP when Production Manager is not on site - Support Production Manager to improve continuously the performance through key performance indicator - Management of waste material; - Support in Health, Safety and Environment management in collaboration with the Production Manager - Support Production Manager on compliance activities and documentation on site with existing statutory and corporate standards in the area of regulatory compliance, cGMP, Health, Safety, and Environmental Protection. Minimum Requirements: Work Experience: - 2 years of experience in a high tech production environment - Scientific background/experience - Radiation safety education - Awareness and strong affinity with quality issues - Soft skills (communication, leadership, team-working with other departments, problem solving) - Open and clear collaboration and communication to make sure the daily production operation runs smoothly - Exploitation of new technology and techniques to eliminate non-value adding activities and improve productivity / performance through new processes - Shows the appropriate sense of urgency around given tasks Languages: - Fluent Italian - Good level of English. Division Operations Business Unit Innovative Medicines Location Italy Site Ivrea Company / Legal Entity IT58 (FCRS = IT058) AAA Italy Srl. Functional Area Technical Operations Job Type Full time Employment Type Temporary (Fixed Term) Shift Work No

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