• Executar testes manuais e apoiar a execução de testes automatizados em sistemas (web, desktop e apps), conforme o planejamento das sprints; • Apoiar na escrita e detalhamento de cenários de testes funcionais; • Registrar e acompanhar o ciclo de vida dos bugs/evidências encontrados nas ferramentas de gestão; • Auxiliar na manutenção e atualização de scripts de automação de testes; • Explorar e experimentar ferramentas de Inteligência Artificial para otimizar suas tarefas diárias de teste.

• Realizar análise e acompanhamento de defeitos identificados pela fábrica de testes. • Apoiar na documentação de processos, evidências e rotinas da área. • Executar testes de conectividade e atividades de troubleshooting básico. • Auxiliar na validação de regras de firewall e integrações entre sistemas. • Realizar consultas básicas em bancos de dados para análise de incidentes. • Utilizar comandos Linux para navegação e validações operacionais. • Apoiar no acompanhamento de microsserviços e monitoramento de ambientes. • Contribuir para a gestão e controle de ativos de tecnologia. • Manter o histórico de registros e evidências das atividades executadas.

• Contractor professional who, with basic knowledge of the most common programming languages, is able to understand the types of issues the application may present, build a mental model of how the software works internally and test the limits of that model, and create/execute automated tests when necessary. • Bachelor's degree or higher (undergraduate and/or lato sensu postgraduate and/or stricto sensu postgraduate) in Information Technology. • Experience as a Senior Test Analyst and with agile development.

• The Senior Specialist, Quality Assurance – Drug Product is responsible for executing quality assurance activities that support clinical and commercial manufacturing operations in compliance with cGMP standards. • This role focuses on batch record review, vendor oversight, and ensuring the accuracy and completeness of GMP documentation across internal and external manufacturing operations. • The individual will work closely with contract manufacturers to support tech transfer, process validation, and routine GMP operations. • Success in this role requires strong attention to detail, the ability to manage multiple priorities, and effective cross functional collaboration to ensure timely batch disposition and compliance. • The position serves as a key contributor within the QA team, supporting inspection readiness and the ongoing operation and continuous improvement of the GMP Quality System, while also providing occasional support for clinical labeling, drug substance contract manufacturing, and other QA activities as needed.