Remote CMC Regulatory Lead, Global Rare Diseases

12 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.

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