08 set - Lucca
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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