CMC Regulatory Affairs Specialist – Global Dossier Expert

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.
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