Lavoro People - Cigliano

Job Description 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 c...

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...

Role purpose:As Single RAN Access system Engineer you will be part of the global Mobile Access Engineering organization unit that aims to deliver the superiority of our Mobile Network design by the best and most innovative design, engineering and optimisation and implementation across Vodafone.You w...

SummaryCreate and drive with scientific technological excellence the formulation development in close collaboration with operations, analytics, engineering and relevant SMEs, QA and the project DPPL. Development activities include among others: formulation and process-design, control strategy, quali...

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 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 ...

Job Description Summary 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 respons...

SummaryThe 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 ...

To lead the Ivrea TRD RLT Pilot plant Quality Control (QC) team by developing and executing strategic plans, providing direction for organizational structure, GMP and safety strategy, lean and continuous improvement initiatives, and people training and development. The QC Head is responsible for ens...

Job Description SummaryThe 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 responsi...

Job Description 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 ...

SummaryCapo turno IIIl capo turno è responsabile della gestione del suo team per eseguire le operazioni di produzione secondo il programma in conformità con le regole HSE e GMP.Esperto di processoFornire supporto tecnico e scientifico in prima linea per tutte le questioni specifiche del processo per...

Job Description 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 ...

SummaryThe Pilot Plant Manufacturing Team Head is responsible to establish and manage the Production unit and ensures the manufacturing program is achieved efficiently within the framework of regulatory compliance and operating within high standards of GMP, HSE, environmental protection and good wor...

Work Your Magic with us!Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dre...