Remote Cmc Regulatory Lead, Global Rare Diseases

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-*****-Ljbffr

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