03 set - Parma
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.
05 set - Siena
Festival del Calcio Italiano
05 set - Torino
Sit
05 set - Torino
Quest Global
05 set - Ostiglia
Adecco