08 set - Prato
Biopharma Careers
Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines.
The role requires a life science degree, fluency in English, and strong experience in regulatory writing across development stages. Location can be Parma HQ or Europe affiliates, with competitive compensation and benefits.
24 set - Milano
3240 Kyndryl Italia
24 set - Gaggiano
Ams Italy
24 set - Orta San Giulio
Cannavacciuologroup
24 set - Sommariva del Bosco
Bachecalavoro