01 ago - Italia
Altro
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
11 ago - Milano
Michael Page International
11 ago - Asti
Jobtome
11 ago - Milano
Hays
11 ago - Savigliano
Alstom