Lavoro Work - Livorno Ferraris

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...

Summary Location: Ivrea, Italy Role Purpose Leads and manages all Drug Product (DP) project activities linked to the development of radiopharmaceutical parenterals (both ready to use and freeze dried products). Supports & coaches team members, participates in scientific teams and contributes to the ...

We are seeking an experienced and visionary Global Application Manager to oversee various Application Managers and contribute significantly to the overall enterprise architecture and IT strategy of our company. The successful candidate will play a crucial role in ensuring the alignment of applicatio...

Summary The 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 (Clinica...

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 ...

SummaryLocation: Colleretto GiacosaRole PurposeResponsible to ensure compliance to cGxP standards for topics within the area of responsibility (during development, transfer, release, and stability), including safety testing, monitoring, and trending. Provide guidance, support, and leadership for imp...

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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 ...

Summary Location: Colleretto Giacosa Role Purpose Responsible to ensure compliance to cGxP standards for topics within the area of responsibility (during development, transfer, release, and stability), including safety testing, monitoring, and trending. Provide guidance, support, and leadership for ...

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...

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, qua...

Summary Capo turno II Il 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 processo Fornire supporto tecnico e scientifico in prima linea per tutte le questioni specifiche del processo...

Entra nel nostro mondo.Trasforma insieme a noi.Quale sarà la tua sfida?Sarai parte attiva della nostra practice Industrial, Mobility & Automotive. Supportiamo sin dal nostro ingresso sul mercato i principali player di riferimento del settore Automotive e Industrial ma non solo. Aiutiamo i nostri cli...

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...

Summary Capo turno II Il 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 processo Fornire supporto tecnico e scientifico in prima linea per tutte le questioni specifiche del processo...