04 set - Parma
Biopharma Careers
pChiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines. /ppThe role requires a life science degree, fluency in English, and strong experience in regulatory writing across development stages. Location can be Parma HQ or Europe affiliates, with competitive compensation and benefits. /p #J-18808-Ljbffr
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