Quality Assurance/control
1 settimana fa
La risorsa assunta si occuperà di fornire supporto alla produzione occupandosi di:
- Gestione e revisione della documentazione GMP
- Formazione sulle procedure operative
- Gestione delle richieste di Change
- Emissione e revisione di SOP, FORM e Master Batch Record
- Identificazione di opportunità di miglioramento per aumentare la compliance alle GMP in produzione
- Supporto alla preparazione e all'esecuzione di audit interni ed esterni
- Supporto alla manutenzione dell'archivio della documentazione GMP relativa al proprio dipartimento.
L'offerta è rivolta a personale appartenente alle Categorie Protette (art.1 - L.68/99), sia Junior che Senior.
Requisiti:
- Laurea in Biologia/CTF/Chimica o ambiti correlati
- Buona conoscenza della lingua inglese
- Esperienza di almeno 6 mesi in ruoli similari o in ambito Qualità/Produzione
Viene offerta assunzione diretta come da CCNL di riferimento, con inquadramento secondo esperienza/capacità.
Orario di lavoro: full-time
Sede di lavoro: Rieti (RI)
Contratto di lavoro: Tempo pieno
Stipendio: a partire da €30.000,00 all'anno
Orario:
- Dal lunedì al venerdì
-
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