04 set - Parma
Biopharma Careers
pChiesi 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. /ppThe 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. /p #J-18808-Ljbffr
06 set - Livorno
FAENZA UNO PROJECT
06 set - Roma
Michael Page International Italia
06 set - Milano
Adecco
06 set - Alessandria
MOM CONSULTING HR PERMANENT RECRUITMENT