Regulatory affairs specialist

We are currently looking for a Regulatory Affairs Specialist. Main activities Support the monitoring of the site's regulatory compliance through the implementation, management and control of the necessary GMP documentation both internal and provided by clients and suppliers; Implement and manage regulatory document storage databases; Support clients in the registration and post-registration phases through the preparation of dossiers (also in e CTD format); Manage consular paperwork for international registrations, coordinating the various external entities (notary, public prosecutor's office, prefecture, consulates and consultants) to issue the appropriate legalized documentation; Support the management of the MIA maintenance practices for the medicines production, preparing the paperwork for variations, communications, authorization/registration for the import of active substances or updating the Site Master File; Main requirements MA degree (CTF/Chemistry, Pharmacy, Biology..); MS degree in Regulatory Affairs is considered a plus; 2 years of experience in similar roles in complex organizations; Knowledge of GMP; English working knowledge; BSP Pharmaceuticals S.p. A is focused on the development and manufacturing of anticancer drugs with high potency and cytotoxic characteristics for the Pharmaceuticals Industry. BSP has been at the forefront in the fight against cancer since 2006. Innovation is the hallmark of BSP with investments in new technologies and production methods in a high containment plant. We are one of the most important Contract Development and Manufacturing Organization (CDMOs) for anticancer drugs. The fight against cancer is ours too. At BSP we believe in an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. We respect the diversity, the different backgrounds and experiences and provide equal opportunity for all. #J-18808-Ljbffr