Eurofarma

Project Manager

• Lead and ensure the execution of strategic projects, ensuring compliance with schedule, cost, scope, quality, and expected benefits
• Act as the focal point for interfacing with strategic stakeholders, influencing decisions and directing priorities
• Manage and prioritize project launches in alignment with the company’s strategy
• Define and track performance indicators (KPIs) and business results for projects
• Conduct risk analyses and propose strategic scenarios to mitigate impacts
• Ensure governance and maintenance of project management systems, developing dashboards and executive reports in Power BI to monitor projects
• Integrate and process data sets with Power Query, ensuring consistency and reliability of information
• Apply artificial intelligence (Microsoft 365 Copilot) to data analysis, insight generation, and team productivity

Senior Project Analyst – PMO Innovation

• Support and monitor the management of strategic and innovation projects.
• Develop and maintain dashboards and performance indicators in Power BI.
• Automate reports, controls and manual routines using advanced Excel, Power Query and automation tools.
• Support digital transformation initiatives, including applying artificial intelligence to projects (task automation, report generation, assisted analysis).
• Participate in meetings with cross-functional teams, providing tactical support to PMO leadership.
• Prepare presentations, status reports and meeting minutes.
• Monitor project timelines, risks, KPIs and project target plans.
• Ensure data quality and keep information up to date in the project management system.
• Support scenario analyses and data collection for decision-making.

Mid-level Project Analyst – Innovation PMO

Analyst

• Gerir o processo ponta a ponta de doação de medicamentos no Brasil, assegurando conformidade regulatória, fiscal e sanitária;
• Garantir rastreabilidade, controle de estoque, validade e documentação das doações;
• Elaborar e implementar fluxos, procedimentos e governança do processo de doação;
• Atuar junto às áreas internas (Comercial, Logística, Fiscal, Qualidade, Jurídico) para viabilização das doações;
• Apoiar tecnicamente as operações internacionais na estruturação e execução de programas de doação, respeitando legislações locais;
• Monitorar indicadores de volume doado, impacto social e eficiência operacional;
• Assegurar aderência a auditorias internas e externas, políticas corporativas e compliance;
• Gerir projetos sociais, garantindo execução conforme planejamento, cronograma, orçamento e metas;
• Integrar iniciativas de doação aos programas de responsabilidade social e estratégia ESG;
• Desenvolver ferramentas de gestão e monitoramento dos projetos;
• Controlar orçamento dos programas, incluindo iniciativas de doação;
• Monitorar desvios e propor ações corretivas;
• Assegurar prestação de contas e governança dos processos;
• Gerir relacionamento com instituições beneficiárias, parceiros técnicos e órgãos reguladores;
• Prospectar e avaliar organizações elegíveis para doação (ex.: entidades certificadas e habilitadas);
• Representar institucionalmente a empresa em fóruns e agendas relacionados a acesso a medicamentos e responsabilidade social;
• Desenvolver indicadores específicos para programas de doação (ex.: acesso, abrangência, perfil dos beneficiários);
• Consolidar dados e gerar análises estratégicas para tomada de decisão;
• Apoiar avaliações de impacto social;
• Elaborar relatórios executivos sobre programas de doação e demais iniciativas sociais;
• Apoiar comunicação institucional e relatórios ESG;
• Reportar resultados para liderança e stakeholders;
• Contribuir para a definição da estratégia de responsabilidade social com foco em acesso a medicamentos;
• Realizar benchmarking de práticas nacionais e internacionais;
• Identificar oportunidades de inovação e expansão do programa de doação.

Analista de Responsabilidade Social Pl

Manager

• Develop and implement the strategic and tactical plan for the products under your responsibility, ensuring sustainable growth and gains in market share;
• Lead the full product management cycle (market analysis, forecast, promotional plan, campaigns, KPI monitoring, sell-in/sell-out, and budget management);
• Prepare and execute product launch and repositioning plans;
• Conduct market, competitor and trend analyses, translating data into actionable strategies;
• Manage the product line budget, ensuring optimized investment and ROI;
• Develop promotional materials and campaigns in compliance with regulatory requirements;
• Collaborate closely with teams such as Sales, Medical, Regulatory Affairs, Supply and Training;
• Support the sales force with strategic training, guidance and regular cycle meetings;
• Build relationships with KOLs and key stakeholders within the specialty;
• Plan and oversee participation in medical events of various sizes (national and regional congresses, etc.).

Senior Product Manager

• The professional will work in the Institutional Relations area, supporting the development, organization and execution of the company’s strategic agendas with external stakeholders relevant to the pharmaceutical sector.
• Monitor and analyze institutional, regulatory and sector-related issues of interest to the company;
• Monitor external scenarios with potential impact on the business;
• Support institutional relationships with strategic stakeholders;
• Prepare briefings, reports, executive presentations and supporting materials;
• Assist in the preparation and follow-up of meetings and institutional agendas;
• Track public policy discussions and proposals relevant to the pharmaceutical sector.

Institutional Relations Analyst, Mid-level

• Critical analysis of the medical literature.
• Provide and make available medical-scientific expertise to support the company’s strategic decision-making.
• Identify unmet needs and propose product improvements and lifecycle strategies.
• Prepare and/or review medical rationale documents related to Eurofarma products.
• Plan and implement medical-scientific activities for the therapeutic areas under your management.
• Review and adapt, as required by local regulations, technical-scientific documents and materials, including the clinical portion of dossiers for product registration (and renewal).
• Prepare the technical-scientific content of local product package inserts and review and approve the final document.
• Identify and develop relationships with local, national, regional and international key opinion leaders (KOLs), medical societies and relevant patient associations.
• Participate in national and international scientific events to update and disseminate clinical knowledge and to strengthen relationships with specialists.
• Coordinate scientific committees.
• Work with access teams, providing scientific support, connecting relevant stakeholders (KOLs, managers and providers), presenting clinical data and supporting continuing medical education initiatives.
• Participate in planning and executing speaker training, including development of scientific materials, selection and engagement of speakers in collaboration with medical leadership, structuring training sessions and pre-sharing scientific content.
• Train internal and external audiences on diseases and treatments, including structured support for sales force training through content development and lectures.
• Plan and implement medical-clinical trainings, including support for CAE and INFOMED.
• Develop and provide scripts addressing the main product objections for which you are responsible.
• Support activities related to product launches, including technical-scientific support, participation in strategic planning, structuring launch events, suggesting and inviting KOLs and speakers, and potentially delivering lectures.
• Plan and participate in scientific events (lectures, symposia, congresses and meetings), including selection and nomination of KOLs, suggesting speakers and scientific topics, as well as delivering lectures and moderating discussions.
• Maintain direct interface with prescribers, responding to medical-scientific questions related to products.
• Review investigator-initiated study requests and Phase IV study requests, follow progress and publish local clinical studies.
• Clinically assess adverse events, providing technical-scientific rationale and monitoring risk/benefit.
• Participate in and support pharmacovigilance activities.
• Participate in internal and external safety committees.
• Review and approve promotional materials, ensuring regulatory and scientific compliance.

Senior Project Analyst – PMO Innovation

Mid-level Project Analyst – Innovation PMO

Analista de Responsabilidade Social Pl

Senior Product Manager

Institutional Relations Analyst, Mid-level

Medical Manager – Mid-level