Major AccountabilitiesAchieve the best product registration with commercially attractive labelling in accordance with registration plan -Maintain and secure product license in terms of CMC/CDS/safety update according to local regulations/law/guidelines, company strategy and integral compliance -Ensure compliance with NP4, KRPIA code of conduct, relevant regulations and laws for related CPO activities (DRAGON update, RMP, packing materials, promotional materials/activities, PMS/drug safety reporting etc.)
-Foster and maintain good relations with internal and external stakeholders -Reporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receipt -Distribution of marketing samples (where applicable)Key Performance IndicatorsProject & stakeholder feedback -Product license update in terms of CMC in agreed timeline -Adherence to Sandoz policy and guidelinesMinimum RequirementsMinimum of 2 years of experience in Regulatory Affairs within Latin American countries.Experience with regulatory submissions and lifecycle management activities for pharmaceutical products.Knowledge of applicable pharmaceutical regulations in at least one Latin American country.Experience using regulatory and quality databases.Proactive, detail-oriented, and capable of managing multiple projects simultaneously.Strong ability to work independently, as the direct manager will be based remotely.
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