LAVORO DESIGN DEVELOPMENT OF DATA PARMA, EMILIA ROMAGNA

design and manage project cards to enable a standardized evaluation of business cases for pipeline projects and collaborate with bd to ensure consistency of treatment...

Experience in change management and governance framework development...       supervise to guarantee the compliance of the validation processes and collaborate on...

We believe that the success of chiesi is built and shaped by our people and our strong set of shared values and behaviors... blois-la chaussée saint victor plant...

Il biotech center of excellence punta sull’innovazione biotecnologica, con particolare attenzione allo sviluppo di anticorpi monoclonali, enzimi e altre proteine...

Periodic drafting of the "table of validated suppliers of raw materials and packaging materials" qualitatively evaluate contractors: collaborates with qa/auh to...

Periodic drafting of the "table of validated suppliers of raw materials and packaging materials" - qualitatively evaluate contractors: collaborates with qa/auh to...

Assist with data entry, assessment, and maintenance of crm systems... each franchise is organized by stage of development with fully empowered and enhanced teams...

Excellent knowledge of the clinical trials settings... support the cross-functional team working on clinical trials transparency, with a particular focus on content...

Basic knowledge of python (e... contributing to the automation of routine tasks in drug design workflows... supporting the integration of cheminformatics and bioinformatics...

Basic knowledge of project management    comprehensive understanding of drug development process... we strive to enhance patients’ well-being and quality...

Each franchise is organized by stage of development with fully empowered and enhanced teams of: pipeline development and commercial portfolio management...

Strong understanding of gcp, regulatory requirements, and clinical trial methodologies...   education medical doctor degree from a renowned institution; certification...

Strong understanding of gcp, regulatory requirements, and clinical trial methodologies... clinical section of the investigator’s brochure, protocols and clinical...

Supply  oversight of the delivery plan in order to grant the continuity of production plan, the right level of stock and escalating in case of risk/opportunities...

We believe that the success of chiesi is built and shaped by our people and our strong set of shared values and behaviors... therefore, we strive to continuously...

Proficiency in data analysis software and tools... maintain detailed and accurate records of experiments and results... design, develop, and execute in vitro pharmacological...

Deep knowledge of gmp/cgmp and guidelines (ich, emea, pqri, health canada) related to the pharmaceutical development of inhalation products...