Lavoro Novartis Pharma Schweiz - Ivrea

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 backup of...

Key Responsibilities Perform Micro / EM analysis of batches according to internal SOPs; Execute process validation protocols, method validation protocols and every study tied to drug products involved in technology transfer for the field of expertise. Promptly report to Quality Control Head and Qual...

The CQV (Commissioning, Qualification and Validation) Engineer provides the Pilot Plant with Subject Matter Expert (SME) knowledge and skills related to commissioning, qualification and validation activities and requirements of facility, utilities and equipment. He is responsible for timely planning...

The MBR Designer plays a pivotal role in supporting Manufacturing Execution Systems (MES) operating sites by providing expert design and business process support. This role is responsible for the delivery and updating of Master Batch Record (MBR) Design Elements, ensuring alignment with global core ...

Key ResponsibilitiesPerform Micro / EM analysis of batches according to internal SOPs;Execute process validation protocols, method validation protocols and every study tied to drug products involved in technology transfer for the field of expertise.Promptly report to Quality Control Head and Qualifi...

Major AccountabilitiesPerform the analysis of batches following specific training.Promptly report to the Quality Control Supervisor and the Qualified Person any deviation and/or out of specification detected during the analysis activities.Collaborate with the Quality Control Head/supervisor for the ...

Major AccountabilitiesEnsure that raw materials used for the manufacturing process are always available in the right amount and properly stored according to their status.Support Production Manager to write down and validate the Standard Operating Procedures and Work Instructions relating to producti...

Major Accountabilities Perform the analysis of batches following specific training. Promptly report to the Quality Control Supervisor and the Qualified Person any deviation and/or out of specification detected during the analysis activities. Collaborate with the Quality Control Head/supervisor for t...

The CQV (Commissioning, Qualification and Validation) Engineer provides the Pilot Plant with Subject Matter Expert (SME) knowledge and skills related to commissioning, qualification and validation activities and requirements of facility, utilities and equipment. He is responsible for timely planning...

Major AccountabilitiesEnsure that raw materials used for the manufacturing process are always available in the right amount and properly stored according to their status.Support Production Manager to write down and validate the Standard Operating Procedures and Work Instructions relating to producti...

Major Accountabilities Ensure that raw materials used for the manufacturing process are always available in the right amount and properly stored according to their status. Support Production Manager to write down and validate the Standard Operating Procedures and Work Instructions relating to produc...

The MBR Designer plays a pivotal role in supporting Manufacturing Execution Systems (MES) operating sites by providing expert design and business process support. This role is responsible for the delivery and updating of Master Batch Record (MBR) Design Elements, ensuring alignment with global core ...