17 set - Parma
Biopharma Careers
Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions.
Invii la sua candidatura dopo aver letto i requisiti di competenza e qualifica per questa posizione, riportati di seguito.
You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines.
The 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. xysqume
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