LAVORO DESIGN DEVELOPMENT OF CONTROL PARMA, EMILIA ROMAGNA

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

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...

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...

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

development and implementation of plant projects: manage and coordinate the development of plant projects, ensuring they are designed, implemented, and monitored...

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

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

Basic knowledge of python (e... contributing to the automation of routine tasks in drug design workflows... participating in the analysis and interpretation of computational...

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...

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

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

Maintain detailed and accurate records of experiments and results... design, develop, and execute in vitro pharmacological assays to evaluate the efficacy and mechanism...

Review of temperature excursions and evaluation the subsequent suitability of the product for use...     assist with investigations and management of the implementation...

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...

Main responsibilities act as point of contact for gmd functions (incl... blois-la chaussée saint victor plant (france), a center of excellence specializing in the...

Maintain accurate documentation of activities and patient interactions... main activities as a patient advocacy intern, you will: support the design and execution...