08 set - Modena
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. 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.
J-18808-Ljbffr
26 set - Ubersetto
Fine Foods & Pharmaceuticals N.T.M.
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Nextar Consulting
26 set - Pavia
Technical Hunters
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