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.
J-18808-Ljbffr
30 set - Torino
Mc Engineering
30 set - Trento
Linkedin
30 set - Bardi
Jd.Com
30 set - Reggio Emilia
Manpower MP PERM CONS CENTRO NORD