Per potenziamento dell'organico Regolatorio della sede di Verona quadro di potenziamento della propria Quality Unit, si seleziona un/a addetto al regulatory affairs con le seguenti competenze Key duties of the job are as below: Writing and updating of EU-CTD (module 3.S); Writing and updating of US DMT type II; Writing and updating of J-DMF; Writing and updating of documentation to obtain or maintain CoS (CEP) at EDQM; Customer technical support; Submission of regulatory documentation worldwide; Regulatory management of changes. Key skill required: Strong multitasking skills, able to manage different project at the same time; Ability or motivation to be in contact with Worldwide customers for regulatory technical support; Fluent in English (knowledge of Portuguese is a Plus); Dynamic, proactive and willing-to-do person; Bachelor Degree in scientific environment; 3 Years Experience as Regulatory Affairs (in API companies or Pharmaceutical groups) or as Quality Assurance; Available to relocate in Verona
Senior Regulatory Affairs Specialist
NEWCHEM
Castel d'Azzano, Veneto
Pubblicato 11 giorni fa
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