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Roche

Regulatory Affairs Specialist

San Jose, Costa Rica

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hirly's read of this role

Seniority
Mid level
Country
CR
Work mode
On-site / unstated
First seen by hirly
9 Nov 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

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

Impacto sostenible

Nuestra responsabilidad va más allá de innovar. Contribuyes a soluciones que responden a los desafíos más urgentes de la salud mientras reducimos nuestro impacto en el planeta. Juntos construimos un entorno laboral más sano, una sociedad más justa y un futuro mejor para las próximas generaciones.

La Oportunidad

Garantizar el registro sanitario y actualizaciones de los productos Roche de manera pronta y oportuna ante las Autoridades Reguladoras de los diferentes países de Centroamérica, Caribe y Venezuela y trabajo conjunto con otras áreas de la organización con el fin de que la innovación llegue lo más rápidamente a los pacientes.

Responsabilidades

  • Ejecutar estrategias de registro innovadoras y basadas en riesgo para acelerar el acceso a nuevas moléculas, renovaciones, cambios post-registro y sitios de fabricación.
  • Garantizar el cumplimiento regulatorio del producto comercial despachado a la región, manteniendo actualizadas las bases de datos y sistemas de Roche.
  • Asegurar el alineamiento con estándares globales y normativas locales en todas las actividades regulatorias asignadas, así como en las herramientas y plataformas internas.
  • Liderar una comunicación proactiva y transversal con áreas clave para dar visibilidad del estatus regulatorio, proteger el suministro y agilizar trámites complejos.

Quién Eres

  • Título profesional en Licenciatura en Farmacia (PharmD) e incorporación activa al Colegio de Farmacéuticos de Costa Rica (COLFAR).
  • Mínimo 6 meses de trayectoria en áreas regulatorias y en la gestión de etiquetado en países de Centroamérica, el Caribe y Venezuela.
  • Mínimo 6 meses de experiencia interactuando con Autoridades Sanitarias, asociaciones de la industria y actores clave del sector.
  • Dominio de las regulaciones sanitarias y de etiquetado vigentes en la región de Centroamérica, Caribe y Venezuela.
  • Comprensión sólida y aplicación de las Buenas Prácticas de Manufactura, Almacenamiento, Distribución y Transporte para productos farmacéuticos.
  • Dominio avanzado del idioma español e inglés (oral y escrito).

Beneficios de reubicación, no disponibles para este puesto de trabajo.

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.

Original posting on Roche's site ↗

Listed on hirly, a job board. hirly is not the employer: Roche is hiring for this role.

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