Since its establishment in 1972, Eurofarma has been operating in the health industry, producing and marketing products and services to improve people's quality of life.
Focused on generating shared value, it operates in the areas of Prescription, Nos-Prescription, Generics, Hospital and Oncology.
It offers over 700 products, over 2,000 SKUs and serves 42 medical specialties.
In Brazil, it covers 100 therapeutic classes, which represent 70% of prescriptions in the entire market.
Operating in 20 countries, with manufacturing facilities in Brazil and industrial parks in six other Latin American countries, it generated net sales of R$ 7.1 billion in 2021, a growth of 23% compared to the previous year, and employs more than 8,100 people.

Eurofarma

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analyst

Eurofarma is a pharmaceutical company that has been caring for health for over 50 years, focusing on a wide range of medical products, including prescription drugs, generics, and oncological medicines. They emphasize innovation through biotechnology and clinical research, and they maintain a commitment to sustainability and corporate responsibility. Eurofarma operates in multiple countries and supports healthcare professionals and consumers through comprehensive educational initiatives and accessible products.

Since its establishment in 1972, Eurofarma has been operating in the health industry, producing and marketing products and services to improve people's quality of life. Focused on generating shared value, it operates in the areas of Prescription, Nos-Prescription, Generics, Hospital and Oncology. It offers over 700 products, over 2,000 SKUs and serves 42 medical specialties. In Brazil, it covers 100 therapeutic classes, which represent 70% of prescriptions in the entire market.

Operating in 20 countries, with manufacturing facilities in Brazil and industrial parks in six other Latin American countries, it generated net sales of R$ 7.1 billion in 2021, a growth of 23% compared to the previous year, and employs more than 8,100 people.

• Realizar a avaliação técnica-regulatória dos documentos gerados pelas áreas de P&D, incluindo Desenvolvimento Analítico, Farmacotécnico, Embalagem, Estabilidade, Equivalência Farmacêutica, entre outros, conforme legislações nacionais e guias internacionais, para elaboração de dossiês e atendimento às exigências de registro de medicamentos e suplemento alimentares na Anvisa e em Agências Regulatórias Internacionais.
• Prestar suporte técnico-regulatório às áreas de interface durante todas as etapas de desenvolvimento de novos produtos.
• Gerenciar e organizar a documentação técnica e promover melhorias contínua nos documentos técnicos, criando modelos-padrão, check lists, entre outros, visando minimizar erros ou falta de informações e otimizar o preenchimento e padronização dos documentos.

Analista de Documentação Técnica – P&D Novos Produtos

Technical Documentation Analyst responsible for evaluating P&D regulatory documents at Eurofarma. Supporting new product development and improving technical documentation processes.

data-analyst

• Design and monitor data pipelines for international market intelligence in our Cloud environments (preferably GCP), ensuring the flow of data from its sources to the end users;
• Monitor and maintain the BI platforms used by the area (currently Power BI) for international market intelligence;
• Collect, handle, and transform different types of data to generate strategic information and recurring patterns for the business;
• Use BI tools (Power BI, etc.) to synthesize large volumes of data and create visual representations that can be easily consulted by end users;
• Interface with different departments to collect and consolidate data in order to generate insights;
• Serve as a communication interface between the business area, the team and the data, and address minor market-related requests.

Data Analyst, Mid-level

Data Analyst at Eurofarma responsible for managing international market intelligence data and reporting. Involves structuring data pipelines and collaborating across multiple business areas.

compliance

• Serve as the focal point for due diligence processes of product dossiers from international partnerships (especially innovative products), evaluating documentation, defining the action plan and tracking it through to dossier submission in the target countries. Lead the project as the primary interlocutor in meetings with partners, internal technical teams and the new business area.
• Carefully assess technical documentation across clinical, pharmacokinetic, manufacturing, pharmaceutics and analytical scopes, identifying and classifying risks and impacts and proposing action plans to resolve or mitigate gaps.
• Prepare core registration dossiers in CTD format to meet the requirements of Brazil and Eurofarma subsidiaries, always mindful of deadlines.
• Lead the development of strategies to respond to regulatory requests and monitor timelines.
• Monitor the creation and evolution of global project schedules, ensuring that development proceeds as planned during technical feasibility assessments and that regulatory and clinical strategies are included in the project timeline. Provide critical oversight of project progress to help prevent major post‑registration delays for product launches in Brazil and LATAM.
• Contribute to updating and disseminating tools for national and international regulatory requirements. Participate in the investigation of requirements for new markets. Stay up to date on changes in health regulations, reflect updates across pipeline projects and ensure that any adjustments required by regulatory updates are implemented.

Senior Regulatory Affairs Analyst

Ensuring compliance with regulations in clinical and pharmaceutical processes at Eurofarma. Leading documentation efforts and liaising with international partners for product submissions.

marketing

• Act strategically and operationally in the execution and monitoring of Trade Channel commercial activities for the OTC business unit, with iconic brands such as Valda and OAZ.
• Ensure excellence in execution of the Trade Marketing plan across different channels, directly contributing to sustainable brand growth and strengthening presence at strategic points of sale (POS).
• Drive brand relevance in the pharmacy and grocery channels, expand distribution and penetration, and ensure alignment between marketing, trade and sales to turn negotiations into long-term strategic partnerships.
• Support the development and preparation of Joint Business Plans (JBPs) with large and mid-sized accounts, contributing personalized plans and strategic alignment;
• Develop the global Trade Marketing calendar, consolidating campaigns, tactical actions, pricing policies, visibility and communication, and defining KPIs by region, channel and brand;
• Perform data analysis and processing to create performance reports, monitoring sell-in, sell-out, distribution activation, campaign ROI, inventories, product mix, market share, coverage and in-store execution (POS);
• Prepare executive results presentations and generate data-driven insights with strategic recommendations on distribution, pricing, promotions and product positioning;
• Conduct ROI analyses of Trade activities, ensuring monitoring, corrections and action plans;
• Support commercial execution by structuring management of negotiations and performance results of activations;
• Manage and monitor Trade budgets, ensuring allocation and use according to the approved plan;
• Work with market tools and audits such as IQVIA, Close Up, Scantech, Dunnhumby and Mtrix, in addition to campaign and budget-management platforms;
• Manage incentive programs and award controls.

Trade Marketing Analyst, Senior

Senior Trade Marketing Analyst at Eurofarma executing trade actions in a strategic and operational capacity. Focused on brand growth and market presence.

support-engineer

• Responsável por desenvolver / pesquisar proposta de formulações viáveis com os recursos da empresa com foco em inclusões de fabricante, manutenção dos produtos de portfólio, promover melhoria contínua nos processos e nas formulações da empresa.
• Além das atividades acima mencionadas, fornecer suporte técnico a todas as áreas da empresa em questões técnicas referentes aos produtos novos e do portfólio, elaboração de documentações para obtenção de registro junto ao órgão regulador (PATE; AR; justificativas técnicas) e conhecimento nas legislações de registro e pós registro (RDC 73; RDC 76, RDC 200, RDC 31, RDC 318, RDC 301)

Farmacotécnico Pl – Transferência de Tecnologia e Suporte Técnico

Farmacotécnico developing viable drug formulations and supporting the technical departments at Eurofarma. Focus on regulatory documentation and continuous improvement in processes.

Since its establishment in 1972, Eurofarma has been operating in the health industry, producing and marketing products and services to improve people's quality of life. Focused on generating shared value, it operates in the areas of Prescription, Nos-Prescription, Generics, Hospital and Oncology. It offers over 700 products, over 2,000 SKUs and serves 42 medical specialties. In Brazil, it covers 100 therapeutic classes, which represent 70% of prescriptions in the entire market. Operating in 20 countries, with manufacturing facilities in Brazil and industrial parks in six other Latin American countries, it generated net sales of R$ 7.1 billion in 2021, a growth of 23% compared to the previous year, and employs more than 8,100 people.

Eurofarma

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