07 set - Ancona
Biopharma Careers
Chiesi seeks a Regulatory Affairs (RA) Senior Manager with strong CMC pre/post-approval experience to support the Global Rare Diseases portfolio. You will lead CMC documentation, author sections, and advise on regulatory strategies across global submissions.
The role emphasizes collaboration with cross-functional teams, external CMOs, and continuous learning in a fast-paced environment. Based in Europe with flexible working options and competitive compensation.
J-18808-Ljbffr
22 set - Biella
KLN Freight (Italy
22 set - Prato
Automatic Ecom
22 set - Arezzo
Human Company
22 set - Venezia
Automatic Ecom