Descripción: Collection of information necessary for the preparation of registration dossiers. ·Monitoring procedures pre and post authorization of the products of the company. ·Answers deficiencies letters ...
Requisitos: ·Education: Degree in Pharmacy, Chemistry or Biology. Master is a plus. ·Languages: Fluent Spanish and English, knowledge of other languages will be an asset. ·Experience (years/area): 1-3 years of experience in the same functions. ·Specific Knowledge: Knowledge of legislation related to DMF (Drug Master File) in CTD format. Knowledge of GMP Regulations. ·Travels: Not required. ·Personal skills: Ability to work in a team and autonomously, multitasking and flexible to schedule changes, ability to work under pressure (short deadlines).