Lavoro Novartis Acc - Ivrea

SummaryClinical Trial Supply Manager (CTSM) defines and executes an optimal clinical trial supply strategy for a clinical trial including effective risk management to ensure supply continuity to patients.The CTSM is the GCS single point of contact at trial level for the integrated CTT (Clinical Tria...

SummaryClinical Trial Supply Manager (CTSM) defines and executes an optimal clinical trial supply strategy for a clinical trial including effective risk management to ensure supply continuity to patients.The CTSM is the GCS single point of contact at trial level for the integrated CTT (Clinical Tria...

SummaryLeads the Pilot Plant Automation function, which is responsible to establish, maintain and improve the automation processes with respect to site buildings, equipment and utilities. He coordinates all automation projects and initiatives, external vendors included. He provides cost-effective, G...

SummaryAs a Micro QC Expert, you will be in charge of the execution and documentation of biological and microbiological testing in conformity to GMP standards and SOPs. Maintenance of the Micro laboratory compliance status and resolution of compliance-related issues. Competency in core activities of...

SummarySupport 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. Act as ba...

Summary As a Micro QC Expert, you will be in charge of the execution and documentation of biological and microbiological testing in conformity to GMP standards and SOPs. Maintenance of the Micro laboratory compliance status and resolution of compliance-related issues. Competency in core activities o...

SummaryLeads the Pilot Plant Automation function, which is responsible to establish, maintain and improve the automation processes with respect to site buildings, equipment and utilities. He coordinates all automation projects and initiatives, external vendors included. He provides cost-effective, G...

SummaryLocation: Ivrea, ItalyRole PurposeDesign, plan and perform Mass Spectrometry experiments as well as report and interpret results/outcome in line with the overall TRD RLT (Radioligand Therapy) project strategy for RLT Drug Substance(s) and Drug Product(s) in development. Ensure project knowled...

Summary Clinical Trial Supply Manager (CTSM) defines and executes an optimal clinical trial supply strategy for a clinical trial including effective risk management to ensure supply continuity to patients. The CTSM is the GCS single point of contact at trial level for the integrated CTT (Clinical Tr...

SummaryThe QC Technician performs the analysis on batches and incoming materials according to cGMP rules and SOPs.About The RoleMajor accountabilities:Perform the analysis of batches following specific training;Promptly report to the Quality Control Supervisor and the Qualified Person any deviation ...

Summary Support 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. Act as b...

Summary The QC Technician performs the analysis on batches and incoming materials according to cGMP rules and SOPs. About The Role Major accountabilities: Perform the analysis of batches following specific training; Promptly report to the Quality Control Supervisor and the Qualified Person any devia...

Summary Leads the Pilot Plant Automation function, which is responsible to establish, maintain and improve the automation processes with respect to site buildings, equipment and utilities. He coordinates all automation projects and initiatives, external vendors included. He provides cost-effective, ...

Summary Location: Ivrea, Italy Role Purpose Design, plan and perform Mass Spectrometry experiments as well as report and interpret results/outcome in line with the overall TRD RLT (Radioligand Therapy) project strategy for RLT Drug Substance(s) and Drug Product(s) in development. Ensure project know...