LAVORO MANAGEMENT ELABORATION OF DATA PARMA, EMILIA ROMAGNA

Purpose the ideal candidate will be responsible for overseeing the global management of product complaints, coordinating the escalation process (girc), and supervising...

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

Support the definition and periodic refresh of the r&d strategy through the collection and elaboration of both qualitative and quantitative information...

Deep understanding of quality management systems, compliance standards, and regulatory requirements within the pharmaceutical sector... experience in change management...

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...

Technical skills - good knowledge and understanding of health care policies of major eu markets - good knowledge of microsoft office applications (microsoft excel...

Assist with data entry, assessment, and maintenance of crm systems... help management team to identify opportunities and threats through analytics...

Excellent knowledge of the clinical trials settings... experience required minimum of 5-8 years of experience in medical writing including as a principal medical...

Basic knowledge of project management    comprehensive understanding of drug development process...   purpose of the role: improving the lives of patients...

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...

Basic knowledge of python (e... supporting the integration of cheminformatics and bioinformatics data into internal platforms and databases...

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

The members of kpmg’s ctr team support organisations across all phases of the process to ensure the security of their information and business strategies...

Main activities assist in the management of various types of agreements (e... assist in the management of intercompany agreements, including the preparation and...

The production area of officine farmaceutiche di parma is the main strategic hub for the production and distribution of chiesi products...     chiesi global manufacturing...

We believe that the success of chiesi is built and shaped by our people and our strong set of shared values and behaviors... the strategy, sustainability & growth...

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...

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

Join us! your data will be processed in full compliance with the provisions of regulation (eu) no... (general data protection regulation - "gdpr") and subsequent...