• Ensure the highest standards of patient safety and data integrity at clinical research sites through regular quality assurance reviews, site quality support, and assurance compliance with Standard Operating Procedures. • Conduct comprehensive reviews of study-specific regulatory binders and clinical documents to verify they are accurately completed and maintained per GCP standards. • Execute the yearly corporate audit plan, systematically tracking quality assurance audits, monitoring related activities, and preparing detailed outcome reports for management. • Partner directly with research staff and Principal Investigators (PIs) to resolve identified compliance issues, developing, tracking, and monitoring Corrective and Preventative Action (CAPA) plans. • Coordinate and provide hands-on operational support for on-site audits and inspections conducted by external providers, sponsors, and regulatory agencies. • Provide ongoing administrative support to the Quality Department by maintaining internal quality systems, compliance trackers, and operational programs. • Participate in the routine review, drafting, and maintenance of quality assurance Standard Operating Procedures (SOPs) to ensure alignment with evolving regulations. • Act as an internal quality resource to provide ongoing guidance and best-practice recommendations to site personnel and clinical project teams. • Be knowledgeable of evolving GxP guidelines. Ability to critically think, eagerness to learn, and commitment to ensuring compliance. Knowledge of and able to interpret regulatory guidance’s such as 21 CFR Part 11/ Part 312, ICH GCP E6 (R3). • Promote a culture of inspections readiness and continuous improvement. Be flexible to work with risk-based audit agendas and shifting priorities. • Create and deliver training on Quality and Improvement activities. • Support completion of RFP/RFI (Request for proposals/information). • Willingness to learn and engage with digital technologies. • Provide AI project quality support and consultation. • Support other activities related to the management of QMS and accuracy of data. • Support GxP and non GxP quality issues and/or projects needing quality consultation and support.

• Diseñar, documentar y ejecutar casos y escenarios de prueba, asegurando una cobertura adecuada según la criticidad del producto • Definir y llevar adelante estrategias de testing que garanticen una visión integral de la calidad • Involucrarte en etapas tempranas del desarrollo, participando activamente del ciclo completo del producto para prevenir defectos desde el inicio • Automatizar pruebas utilizando herramientas como Selenium IDE, contribuyendo a la eficiencia y escalabilidad del proceso de QA • Validar APIs REST y SOAP, así como aplicaciones mobile, asegurando el correcto funcionamiento funcional y técnico

• Take charge of the entire lifecycle of customer engagements in cybersecurity • Simulate attacks on computer systems, networks, applications, and digital assets • Conduct comprehensive assessments to identify problem areas • Present visionary solutions to customers and craft personalized proposals • Collaborate closely with other teams to disseminate vital information and recommended countermeasures • Document testing processes, findings, and insightful recommendations

• Gestionar el control documental de los proyectos. • Elaborar y administrar minutas de reuniones. • Realizar seguimiento de acuerdos y compromisos. • Gestionar el versionamiento de documentación. • Administrar repositorios documentales. • Asegurar el cumplimiento de estándares de calidad documental. • Ejecutar revisiones utilizando checklists de calidad. • Brindar soporte metodológico a los equipos de proyecto.