Head of Corporate Quality System

1 settimana fa

Milano, Italia GIGROUP A tempo pieno

HiRevo LifeScience è la specializzazione di Gi Group, prima multinazionale del lavoro italiana, dedicata alla ricerca e selezione di profili in ambito Sales &
Marketing, Clinical Research, R&
D, Regulatory e Operation dei settori Farmaceutico e Medicale.
Il nostro cliente è una storica azienda farmaceutica italiana, presente sul territorio con R&
D, Produzione, ed una prestigiosa Sede centrale - con funzioni Corporate ed Italia - a cui fa capo la Rete di Informazione Scientifica. L’azienda commercializza farmaci, integratori e dispositivi medici.
In fase di riorganizzazione della Direzione Quality, ricerca il/la
Head of Corporate Quality System
che a riporto dell’Head of Corporate Quality avrà tre principali aree di responsabilità
- Quality System Management. Su tale ambito l’Head of Corporate Quality System si occuperà dello sviluppo e del mantenimento del Sistema di Gestione della Qualità, della razionalizzazione del sistema documentale e dell’architettura delle procedure. Gestirà inoltre l’implementazione di un sistema di automatizzazione. Assicurerà l’aderenza alle disposizioni legislative vigenti in relazione alle GXP (GCLP, GLP, GCP, GMP, GDP, GVP) e la Compliance alle ISO e supporterà la Direzione Quality Corporate nella definizione delle policies generali in materia di Qualità.
- Quality Assurance Third party. Rispetto ai terzisti e all’Assicurazione Qualità terze parti, l’Head of Corporate Quality System si occuperà della stesura dei Quality Technical Agreement e del monitoraggio delle performance.
- MDR e ISO13485 sarà responsabile della gestione del sistema di qualità relativo dei Dispositivi Medici di cui l’azienda cliente risulta Fabbricante o Distributore e supporterà il PRRC nello svolgimento delle attività di propria competenza.

La ricerca è orientata verso professionisti con esperienza consolidata in Qualità maturata nel settore farmaceutico, nello specifico nella Gestione del Sistema Qualità, nel Quality Assurace terze parti e/o nelle Quality Operations di stabilimenti farmaceutici GMP.

La certificazione di Auditor e la qualifica di QP rappresentano un plus.

Si offre contratto a tempo indeterminato, ccnl chimico farmaceutico, ral e inquadramento in funzione dell’esperienza.

Gi Group S.P.A. è autorizzata ad operare dal Ministero del Lavoro (Aut. Min. 26/11/2004 PROT. 1101 - SG).

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