Your Responsibilities :
La risorsa, inserita nel reparto di Engineering Validation del sito di Verona, si occuperà delle attività di convalida di macchine di produzione, utilities critiche e sistemi computerizzati di controllo e monitoraggio rispettando le regole GMP.
La risorsa selezionata, al termine dello stage, avrà acquisito una conoscenza generale del processo produttivo di riempimento asettico di antibiotici iniettabili, una conoscenze delle principali normative farmaceutiche (cGMP, CFR) applicate nell'ambito della convalida di sistemi.
Basic qualifications :
Laurea Scientifica (Ingegneria chimica, Chimica e Tecnologie Farmaceutiche)
Buona conoscenza di Office, in particolare di Excel
Preferred qualifications :
Why GSK? :
GSK is deeply committed to professional and personal development offering employment opportunities across a diverse collection of businesses and geographies.
So you'll flourish in an inspiring environment where personal growth plays a vital part in the changing face of the business.
Most of all, you'll enjoy the sense of purpose that comes from leading change in an industry that touches millions every day.
We offer :
Contact information :
You may apply for this position online by selecting the Apply now button.
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