07 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.
Pronto/a a candidarsi? Prima di farlo, si assicuri di leggere tutti i dettagli relativi a questo lavoro nella descrizione sottostante.
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. xbvzest
J-18808-Ljbffr
Per questa posizione sono disponibili opzioni di lavoro a distanza/a casa.
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