Quality Assurance Consultant

5 giorni fa


Liguria, Italia Confidenziale A tempo pieno

supporto al team di Compliance per la gestione delle attivit relative al sistema di Qualit aziendale, quali redazione, revisione delle Standard Operating Procedures (SOPs) e del Web Information System (WIs) adeguamentoe mantenimento del Quality Management Software (QMS) in conformit agli Standard Regolatori attivit di training GMP rivolte al personale interno di sito gestione delle principali attivit in ambito Quality Assurance, comprese CAPA, deviazioni e change Requisiti richiesti dal ruolo:
laurea in discipline scientifiche esperienza nella scrittura, revisione, archiviazione di Standard Operating Procedures conoscenza delle linee guida internazionali, in particolare EU GMP parte 11, Code Federal regulation (CFR) 21 Part 820 e 821, e le ISO 9001, ISO 15378 e ISO 13485 dimestichezza nellutilizzo di sistemi software di gestione qualit conoscenza avanzata del pacchetto Office forte attitudine al problem solving spiccate doti comunicative e relazionali Sar considerato un plus laver avuto precedenti esperienze in stabilimenti farmaceutici specializzati nella manifattura di prodotti sterili (es. prodotti per uso parenterale). Sede di lavoro:
provincia di Padova per la durata del progetto per poi essere allocati presso una delle nostre sedi (Sesto Fiorentino o Parma). Modalit di lavoro:
formula mista ufficio/smart working.



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