QA on the floor
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In questa posizione ti occupi di presidiare le attività produttive secondo GMP, supportando la gestione di deviazioni, non conformità e CAPA. Lavorerai a stretto contatto con Produzione, QC e Ingegneria per migliorare i processi e garantire audit interni ed esterni. L’opportunità è in un’azienda chimico-farmaceutica in forte crescita nei pressi di Milano, con responsabilità di documentazione GMP e conformità operativa. Un ruolo chiave per contribuire al miglioramento continuo e alla conformità normativa, in un contesto strutturato e regolamentato. In questa funzione lavorerai su tre turni lunedì–venerdì, con prospettive di crescita professionale e stabilità.
Responsabilità- Presiedere attività produttive assicurando GMP e procedure qualità
- Supportare il personale di produzione nella gestione di deviazioni, non conformità e change control
- Revisionare la documentazione di reparto (batch record, logbook, istruzioni operative)
- Partecipare alle indagini di deviazione e definire CAPA
- Collaborare con Produzione, QC e Ingegneria per il miglioramento continuo
- Supportare attività ispettive e audit interni/esterni
- Verificare l’applicazione delle procedure e delle istruzioni operative in reparto
- Laurea in discipline scientifiche (Chimica, CTF, Biotecnologie o affini)
- Esperienza pregressa in Quality Assurance di stabilimento in ambito farmaceutico
- Conoscenza delle normative GMP e dei principali processi produttivi
- Buona gestione della documentazione GMP
- Familiarità con ambienti regolamentati e contesti produttivi strutturati
- Buona conoscenza della lingua inglese
- lavoro di squadra
- comunicazione chiara
- precisione e attenzione al dettaglio
- GMP e normative farmaceutiche
- Quality Assurance in stabilimento farmaceutico
- deviation investigations
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