Regulatory affairs specialist

14 ore fa


Florence, Italia Manpower A tempo pieno

Talent Solutions, part of Manpower Group, for an important pharmaceutical client based in Florence, is currently recruiting for aREGULATORY AFFAIRS SPECIALISTWithin the Global Regulatory Affairs department - EU and North America area (EUNA), we are looking for a Regulatory Affairs Specialist with a direct report to the EUNA Therapeutic Area Manager. The resource will be responsible of handling a specific portfolio of products, guaranteeing the obtainment of new registrations and/or the maintenance of the existing ones in the Region in scope.MAIN ACTIVITIES AND RESPONSIBILITIESWithin the EUNA Regulatory Affairs team and under the guidance of the Therapeutic Area Manager, the resource will deal with the registrations and/or life cycle maintenance activities of the products in the specialty and primary care area. It will include, at least:Planning/organizing activities for preparing new product registration and/or maintenance of the existing registration through variation procedures and renewalsWorking in cooperation with technical internal functions (such as Quality Assurance, Medical, Marketing, Clinical, Pharmacovigilance), and local regulatory teams or external partners for the preparation of the regulatory application related to new registrations and/or lifecycle managementPreparation of the master data package to be shared with the local regulatory affairs contacts in order to proceed with the customization, as necessary, and submission of the application to the competent Authority/iesPreparation and management of the paediatric application and relevant update, if anyApplication of the existing working flows and Company proceduresMonitoring and understanding of new RA regulations and guidelines for the area of responsibility.JOB REQUIREMENTSBachelor Degree in scientific environment, including, but not limited to, Pharmacy, Pharmaceutical Chemistry and Technology, Biology, Biotechnology, Chemistry, is mandatoryAt least 3 years of previous experience in an international regulatory affairs department for pharma productsFluent in English, both written and oraldynamic, proactive and willing-to-do profileExcellent interpersonal, organizational and communication skills, capability in working in a team and good problem-solving attitude.



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