08 set - Lecco
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.
25 set - Roma
DAVID NAMAN
25 set - Udine
OLTRE I CONFINI 2.0
25 set - Friuli-Venezia Giulia
Arethusa
25 set - Pescara
Alll