• Garantir a qualidade dos produtos de software por meio da elaboração, execução e acompanhamento de testes • Compreender as regras de negócio • Antecipar riscos e questionar requisitos • Atuar como parceira dos times de Produto, Desenvolvimento e Suporte • Identificar falhas antes da entrega ao cliente • Validar funcionalidades e registrar evidências • Acompanhar correções junto ao time de desenvolvimento • Contribuir para a evolução contínua da qualidade dos sistemas • Elaborar cenários e casos de teste • Executar testes funcionais, exploratórios, de homologação e validação • Garantir que os critérios de aceite sejam atendidos antes da entrega • Participar das cerimônias de desenvolvimento contribuindo com a visão de qualidade • Trabalhar em conjunto com Produto, Desenvolvimento e Suporte para melhoria contínua do software • Identificar riscos técnicos e funcionais antes da implementação • Sugerir melhorias nos processos de testes, desenvolvimento e qualidade do produto • Elaborar planos de teste • Organizar massa de testes.

• Define, plan, and implement automated testing strategies (Frontend and Backend) to ensure end-to-end quality across user acquisition journeys; • Collaborate closely with Product and Engineering teams from conception (Shift-Left Testing), reviewing architectural requirements and acceptance criteria; • Ensure stability of the development pipeline by integrating and maintaining test suites in CI/CD pipelines; • Monitor and validate critical quality and performance metrics (such as Core Web Vitals) that directly impact the organic ranking of the group's brands; • Promote a culture of quality within the multidisciplinary team, serving as a reference and mentor in QA best practices.

Role Description Join our Quality Assurance department as a Quality Assurance Manager. The Quality Assurance Manager is responsible for supervision of the quality management system within an organization, including its development, implementation, and maintenance. Position is in Lithuania or any EU country. - Develop, review, and manage standard operating procedures (SOP’s) of the company processes by assuring conformance with local and international requirements and standards. - Assure the effectiveness and continuing improvement of the quality management system, that clinical trials, pharmacovigilance, regulatory affairs, and good clinical practice training services conform to applicable regulations, good clinical, pharmacovigilance (GVP), good Clinical practice (GCP) or other applicable practice guidelines, ISO 9001, ISP13485 and ISO27001 standards requirements. - Conduct GxP audits according to the agreements with clients and/or internal audits programs. - Manage vendors’ quality assessments and audits. - Coordinate activities during second, third party audits or regulatory GCP and GVP inspections in the company and manage corrective and preventive actions plans after the audits. - Complete and manage quality management system documentation and required accountability forms. - Identify non-compliances, present, and discuss the audits findings, oversee implementation, and control effectiveness of corrective and preventive action plans, provide recommendations for improvement. - Assist in performing root-cause analysis and other problem-solving activities to identify effective corrective actions and process improvement in collaboration with the personnel. - Participate in the training process of the staff by preparing and presenting quality and legal requirements relevant trainings. - Implement and monitor processes that ensure quality. - Provide assistance for all quality management activities. Qualifications - Higher education in Life Sciences (e.g., Pharmacy, Medicine, Biology, Biotechnology, or a related discipline). - Knowledge of EU Good Pharmacovigilance Practices (GVP) is required; knowledge of Good Clinical Practice (GCP) is considered an advantage. - At least 5 years of experience in a pharmacovigilance and/or clinical research environment, including quality assurance experience related to GVP and/or GCP activities. - Knowledge of other GxP requirements, as well as ISO 9001, ISO27001 and ISO13485 standards, would be considered an advantage. - Strong computer literacy and experience with eLMS, eQMS programs. - Ability to develop quality management systems and procedures. - Professional level in English, both in oral and written communications. - Ability to apply critical thinking and problem-solving skills. - Excellent presentation, written and oral communication skills. Benefits - Professional growth and career opportunities. - International team and environment. - Bonus based on annual performance. - Personal accident and business trip insurance. - Additional health insurance. - Influenza vaccines. - Rewarding referral policy. - Team building, global meetings, B active events.

• Develop, review, and manage standard operating procedures (SOP’s) of the company processes by assuring conformance with local and international requirements and standards • Assure the effectiveness and continuing improvement of the quality management system, that clinical trials, pharmacovigilance, regulatory affairs, and good clinical practice training services conform to applicable regulations, good clinical, pharmacovigilance (GVP), good Clinical practice (GCP) or other applicable practice guidelines, ISO 9001, ISP13485 and ISO27001 standards requirements • Conduct GxP audits according to the agreements with clients and/or internal audits programs • Manage vendors’ quality assessments and audits • Coordinate activities during second, third party audits or regulatory GCP and GVP inspections in the company and manages corrective and preventive actions plans after the audits • Complete and manage quality management system documentation and required accountability forms • Identify non-compliances, present, and discuss the audits findings, oversee implementation, and control effectiveness of corrective and preventive action plans, provide recommendations for improvement • Assist in performing root-cause analysis and other problem-solving activities to identify effective corrective actions and process improvement in collaboration with the personnel • Participate in the training process of the staff by preparing and presenting quality and legal requirements relevant trainings • Implement and monitor processes that ensure quality • Provide assistance for all quality management activities