Qc Mrna Material Readiness

5 mesi fa

Monza, Italia Thermo Fisher Scientific A tempo pieno

Thermo Fisher Scientific Inc. ha come missione di rendere il mondo più sano, più pulito e più sicuro. Sia che i nostri clienti stiano portando avanti la ricerca nel campo delle scienze della vita, risolvendo complesse sfide analitiche, aumentando l'efficienza nei loro laboratori, migliorando la salute dei pazienti attraverso la diagnostica o lo sviluppo e la produzione di terapie che cambiano la vita, siamo qui per supportarli.

Il gruppo **mRNA** sta cercando un operatore per **QC mRNA Material readiness** per il sito di Monza.

La risorsa identificata avrà l'opportunità di occuparsi di:

- esecuzione attività di campionamento dei materiali GMP, materiali primari e secondari. Le attività di campionamento verranno svolte sia presso il magazzino interno ThermoFisher che presso il magazzino esterno Vercesi;
- esecuzione campionamenti straordinari di prodotto finito;
- gestire le richieste di certificati e documenti necessari per garantire l'approvazione del materiali, sia a fornitori che clienti;
- esecuzione attività di etichettatura respinto a fronte di documentazione di respingimento ricevuta;
- collaborare con il Team Leader/supervisor in modo tale da contribuire all'ottimale esecuzione delle attività nel rispetto delle GMP, dei metodi e degli standard di qualità aziendale, garantendo lo stato di avanzamento delle stesse nel rispetto delle priorità definite;
- collaborare interne con reparto magazzino, ufficio regolatorio e laboratori;
La risorsa sarà inoltre responsabile di assicurare la corretta gestione della documentazione di competenza, dalla ricezione, al controllo, l'archiviazione e la tracciabilità, sia essa di origine interna che esterna, secondo le procedure vigenti e gli standard qualitativi aziendali. Sarà inoltre responsabile di comunicare tempestivamente eventuali anomalie al proprio team leader/supervisor.

Entrando a far parte del team mRNA, farai parte di un ambiente dinamico e orientato ai risultati e acquisirai un'esperienza approfondita delle attività relative al controllo qualità che sta a monte della produzione GMP.

Un background nel contesto tecnico/farmaceutico, la voglia di mettersi in gioco, e l'interesse ad entrare a far parte di una grande CDMO sono elementi importanti per accedere a questa opportunità di carriera

Unisciti a noi

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