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Regulatory Affairs Manager

2 ore fa


milano, Italia Randstad Italy A tempo pieno

Regulatory Affairs Manager Randstad Italy•Milano, Lombardia, ItaliaFor a multinational company in the pharmaceutical field we are looking for a Regulatory Affairs Manager.The Regulatory Affairs Manager is responsible for managing regulatory activities for an assigned product portfolio. The goal is to secure and maintain marketing authorizations, ensure compliance with local and EU regulations, review promotional materials, and support internal functions in business development.Work site: Milano and 2 smart working daysContract: 12 months fixed termRetribuzione annua: 40000€ - 50000€esperienza2 anniRequirementsDegree in Pharmacy, Chemistry, Biology, or a related field.Minimum of 2 years of operational experience in Regulatory Affairs.In-depth knowledge of National and European regulations and experience in their daily application.Native-level Italian (or equivalent) and fluent in English.Skills & AbilitiesProven ability to manage projects and prioritize tasks.Excellent communication skills and a strong attitude for teamwork within matrix organizations.Detail-oriented with a strong sense of responsibility and the ability to adapt to new systems and procedures.Ability to use AI tools to support daily activitiesLa ricerca è rivolta ai candidati ambosessi (L.903/77). Ti preghiamo di leggere l'informativa sulla privacy Randstad ai sensi dell'art. 13 del Regolamento (UE) 2016/679 sulla protezione dei dati (GDPR).Key ResponsibilitiesEnsure regulatory approval for new products, formulations, or indications and maintain existing Marketing Authorizations (MA), including variations via National, MRP, and Centralized procedures.Manage the end-to-end process of translation and implementation of labelling materials for assigned products.Coordinate activities related to educational materials from Risk Management Plans (RMP) and Direct Healthcare Professional Communications (DHPC) as required by Regulatory Authorities, overseeing local implementation.Provide regulatory expertise within cross-functional teams (including Market Access, Medical, Marketing, Sales, Pharmacovigilance, Quality, Finance, etc.).Evaluate and review promotional and congress materials to ensure compliance with local requirements and Corporate Procedures.Support inspections and audits by providing appropriate regulatory input.Contribute to the development and optimization of regulatory processes and Standard Operating Procedures (SOPs).Guarantee full compliance in alignment with local regulations and Corporate Procedures.#J-18808-Ljbffr