Quality Assurance On The Floor
1 giorno fa
Inclusyon è la società di ricerca e selezione specializzata nel recruiting di personale qualificato appartenente alle categorie protette. Conoscenza dettagliata della normativa (Legge 68/99) e consolidata esperienza in ambito HR si fondono in un approccio consulenziale in grado di soddisfare le esigenze di recruitment della tua azienda, in qualunque settore e per qualsiasi profilo professionale.
**Posizione**:
Inclusyon è la **società di ricerca e selezione** specializzata nel recruiting di personale qualificato appartenente alle **categorie protette**.
**Il contesto**:
Per importante società corporativa giapponese attiva nel settore chimico-farmaceutico, Inclusyon ricerca un/una **Quality Assurance on the floor - categorie protette Legge 68/99**.
**Il ruolo**:
- Eseguire le attività di QA on the shop floor nelle aree di produzione, magazzino e laboratori QC promuovendo il rispetto delle cGMP e il miglioramento continuo.
- Supervisionare le attività relative al media fill al fine di garantirne la corretta esecuzione e supportare la stesura del report finale.
- Supportare la definizione dei piani di campionamento microbiologici e particellari.
- Eseguire la stesura/revisione di procedure di reparto (SOP, Work Instructions,etc.).
- Eseguire le attività di audit trail review delle operazioni di produzione e relativamente al monitoraggio degli ambienti di produzione (sistemi SCADA), provvedere alla gestione degli allarmi.
- Revisionare i logbook di produzione.
- Eseguire le investigazioni a seguito di deviazione e provvedere all’eventuale definizione ed implementazione di azioni correttive, preventive e/o di miglioramento.
**Requisiti**:
**Requisiti primari**:
- Diploma di Laurea in discipline tecnico-scientifiche (Biologia, Biotecnologie, CTF, Farmacia o equivalenti).
- Ottima conoscenza della lingua inglese.
- Capacità di lavoro in team e comunicative, ascolto attivo, occhio al dettaglio e autonomia.
**Requisiti secondari**:
- Conoscenza delle principali regulations e linee guida internazionali in ambito farmaceutico (GMP, EU GMP, Decreto Legislativo 219, ISO 9001:2015).
**Altre informazioni**:
Sede di lavoro: Pisa.
Orario di lavoro: 9:00 - 18:00.
Tipologia contrattuale: Contratto a tempo indeterminato.
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