Assistente di Produzione

Recordati has been at the forefront of life-enhancing and life-changing medicines for almost 100 years. With its beginnings in a family run pharmacy in Correggio, Italy in the 1920s, Recordati is now a global pharmaceutical force, listed on the Italian stock exchange, with over 4,200 employees._
- We are a group of like-minded, passionate individuals who go to extraordinary lengths for our partners, customers, investors and the people across the globe who we serve. We develop and commercialise medicines to serve people living with common diseases, as well as those living with some of the rarest, in around 150 countries._

**Descrizione del ruolo**

La risorsa affiancherà e supporterà il responsabile ed i coordinatori in turno del reparto confezionamento per tutte le attività inerenti la gestione delle linee di produzione.

**Responsabilità principali**
- Gestione dei sistemi computerizzati di reparto in accordo ai requisiti di Data Integrity;
- Revisione ed implementazione delle procedure GMP dei reparti di produzione;
- Cooperazione con gli altri reparti (Manutenzione, Controllo Qualità, Assicurazione Qualità, Pianificazione e Logistica) al fine di assicurare il miglior supporto allo svolgimento delle attività attraverso la risoluzione di problematiche in corso;
- Supporto dell'organizzazione della produzione al fine di conseguire gli standard qualitativi e quantitativi richiesti.

**Requisiti**
- Padronanza nella gestione della documentazione relativa ai processi produttivi;
- Conoscenza consolidata delle norme GMP, delle procedure di vestizione, di processo e delle regole relative alla data integrity;
- Competenze relative ai principi di Lean Manufacturing;
- Esperienza pregressa nel monitoraggio e applicazione delle corrette pratiche HSE;
- Capacità ed esperienza nella gestione del personale di produzione.

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**Role description**

The resource will support the department manager and shift production supervisors for all activities related to production line management.

**Main Responsibilities.**
- Management of departmental computer systems in accordance with Data Integrity requirements;
- Review and implementation of the GMP procedures of the production departments;
- Cooperation with other departments (Maintenance, Quality Control, Quality Assurance, Planning and Logistics) in order to ensure the best support for carrying out activities through the resolution of ongoing problems;
- Support of the production organization in order to achieve the required qualitative and quantitative standards.

**Requirements**:

- Knowledge in managing documentation related to production processes;
- Well-established knowledge of GMP standards, dressing procedures, process and rules related to data integrity;
- Skills related to Lean Manufacturing principles;
- Prior experience in monitoring and enforcing proper HSE practices;
- Ability and experience in managing production personnel.
- At Recordati, we believe in equal opportunities and we guarantee that everyone can achieve their potential. We see diversity as a value and will not tolerate any discrimination based on ethnicity, nationality, gender, sexual orientation, disability, age, political or religious belief, or any other personal characteristics. At Recordati, we work hard to create a safe and inclusive work environment, where we all have our rights to physical and psychological integrity respected on a daily basis, as well as our right to freedom of opinion and association. We recognise that we each have a role to play in the success of our business and we implement staff development policies through which everyone's contribution and achievements can be appropriately rewarded._