A global pharmaceutical company in Turbigo is seeking a Regulatory Affairs CMC Specialist to manage dossier preparations for regulatory submissions. This role requires a degree in chemistry, pharmacy, or biotechnology, and at least 3 years of experience in CMC regulatory affairs. Responsibilities include writing technical sections, conducting assessments, and ensuring compliance with regulatory guidelines. The ideal candidate should have strong analytical skills and be fluent in English, in a collaborative and diverse environment.#J-18808-Ljbffr
Cmc Regulatory Affairs Specialist – Global Dossier Expert
RECORDATI
turbigo, turbigo
Pubblicato 12 giorni fa
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