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In office (Bogotá)
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Intern
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Full-Time
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Roche is a Swiss healthcare group founded in Basel in 1896 and is unusual in operating two large divisions of comparable importance: prescription medicines and in vitro diagnostics. The pharmaceutical business is built on oncology, neurology, immunology, ophthalmology and haemophilia, with products such as Ocrevus, Hemlibra, Perjeta and Vabysmo, while the diagnostics division supplies laboratory analysers, molecular tests and sequencing systems to hospitals worldwide. The group owns the American biotechnology company Genentech outright and the Japanese firm Chugai in majority, is controlled by a family shareholder pool, and spends among the largest research budgets in the industry.

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

Objetivo del Puesto:

Brindar apoyo a equipos de Asuntos Regulatorios, Calidad, Farmacovigilancia, Estudios Clínicos; en actividades relacionadas con la gestión de sometimientos regulatorios, sistema de gestión de calidad y farmacovigilancia/tecnovigilancialo que le permitirá familiarizarse con las funciones de estas áreas de la industria farmacéutica y diagnóstica . Además, proporcionará soporte a las áreas correspondientes, apoyando el cumplimiento de las normativas nacionales e internacionales.

Responsabilidades:

  • Colaborar en la preparación y revisión de expedientes regulatorios para la presentación ante autoridades sanitarias.

  • Apoyar en la actualización y mantenimiento de bases de datos regulatorias.

  • Asistir en la recopilación y organización de documentación técnica y científica necesaria para las presentaciones regulatorias.

  • Realizar seguimiento de los procesos y plazos regulatorios, asegurando el cumplimiento de los mismos.

  • Participar en la elaboración de informes y reportes requeridos por las autoridades regulatorias.

  • Contribuir en la revisión y traducción de documentos regulatorios y científicos.

  • Mantenerse actualizado sobre cambios en la normativa regulatoria y comunicar dicha información al equipo.

  • Apoyar la documentación y evaluación de situaciones de seguridad, preparación de información de seguridad, reconciliación de casos y soporte a diferentes programas que conectar con la red.

  • Colaborar en la preparación y revisión de expedientes regulatorios para la presentación ante autoridades sanitarias.

Requisitos:

  • Estudiante activo de las carreras de: Química Farmacéutica, Enfermería, Ciencias de la Salud (médico, bacteriólogo, enfermería o carreras a fines)e Ingeniería Biomédica

  • Inglés intermedio

  • Disponibilidad de laborar jornada continua.

Who we are

A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.

Let’s build a healthier future, together.

Roche is an Equal Opportunity Employer.

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