Regulatory Affairs Specialist

3 settimane fa


Siena, Italia AKKA TECHNOLOGIES A tempo pieno

Akkodis è un leader globale nel mercato dell'ingegneria e della ricerca e sviluppo che mira ad accelerare l'innovazione e la trasformazione digitale utilizzando la forza dei connected data. Con la passione per la tecnologia e il talento, il gruppo composto da 50.000 ingegneri ed esperti digitali offre una profonda esperienza intersettoriale in 30 paesi tra Nord America, EMEA e APAC.

Akkodis vanta un’ampia esperienza e un forte know-how in settori tecnologici chiave come la mobilità, i servizi software e tecnologici, la robotica, i test, le simulazioni, la sicurezza dei dati, l'intelligenza artificiale e l'analisi dei dati.

La combinazione di competenze informatiche e ingegneristiche porta a un'offerta unica di soluzioni end-to-end, con quattro linee di servizio - Consulting, Solutions, Talents e Academy - per supportare i clienti nel ripensare ai loro processi di sviluppo prodotto e di business, migliorare la produttività, ridurre al minimo il time-to-market e dare forma a un domani più smart e sostenibile.

Akkodis fa parte del Gruppo Adecco.
Akkodis è un marchio commerciale sotto il quale operano AKKA e Modis.

Nell’ottica di un potenziamento del team, ricerchiamo una figura di:
**Regulatory Affairs Specialist - Pharma**

La risorsa, inserita all'interno della BU di Process & Quality, si occuperà delle seguenti attività, sia per il settore farmaceutico che delle terapie avanzate:

- Scrittura **CTD **(Common Technical Document)
- Allestimento **variazioni**:

- Supporto per la scrittura di **IMPD **(Investigational Medicinal Product Dossier) e **PSF **(Product Specification File)

**Requisiti**

Sono richieste le seguenti competenze:

- Esperienza in **ambito regolatorio**:

- Scrittura **CTD**:

- Conoscenza delle **GMP**

**Offerta**

Tempo Indeterminato

**Location**

Sono previste assunzioni sulle nostre sedi di Milano, Poggibonsi e Pomezia.



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