Global Regulatory Affairs Associate

Talent Solution, part of Manpower Group, for an important pharmaceutical client based in Florence, is currently recruiting a motivated Regulatory Affairs Associate, within the Global Regulatory Affairs department Rest of the World (RoW), 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 RESPONSIBILITIES The resource will deal with the registrations and/or life cycle maintenance activities of the products in the area.
It will include, at least: - Planning/organising activities for preparing new product registration and maintenance of the existing registration through variation procedures and renewals, - Working in cooperation with technical internal functions (such as Quality Assurance, Medical-marketing, Clinical Sciences, Pharmacovigilance), and local regulatory teams or external partners for the preparation of the regulatory application related to new registrations and lifecycle management, - Preparation 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/ies - pplication of the existing working flows and Company procedures - Monitoring and understanding of new RA regulations and guidelines for the area of responsibility.
JOB REQUIREMENTS - Degree in scientific environment, including, but not limited to, Pharmacy, Pharmaceutical Chemistry and Technology, Biology, Biotechnology, Chemistry, is mandatory, - a Master or a previous experience in the regulatory environment is preferred, - Fluent in English, both written and oral, The candidates should be dynamic, proactive and with excellent interpersonal, organizational and communication skills, capability in working in a team and good problem-solving attitude.
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