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Asistente de Asuntos Regulatorios

PSF14 open roles

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Asunción, Asuncion, Paraguay
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Your applicationOpen nowAsistente de Asuntos RegulatoriosPSF · Asunción, Asuncion, Paraguay
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The clock on this job

Early applications get read.

13.5% of postings close within 7 days. Measured by our own scanner across the market. PSF postings stay open a median of 2 days.

Share of postings closed within
  1. 2.3%1 day
  2. 4.6%3 days
  3. 13.5%7 days
  4. 21.8%14 days
  5. 36.6%30 days
  6. 58.9%60 days
This job: posted today

PSF median: 2 days open

The posting

Descripción del puesto

Descripción del puesto: Asistente de Asuntos Regulatorios

En nuestro equipo, el rol de Asistente de Asuntos Regulatorios es fundamental para garantizar que todas nuestras operaciones se alineen con las regulaciones vigentes. Buscamos a alguien con una sólida formación universitaria, que esté listo para sumarse a un ambiente que valora la responsabilidad y la excelencia.

Tu día a día incluirá la colaboración en la preparación y presentación de documentación ante entidades regulatorias, asegurando que cada proceso cumpla con los estándares requeridos. Además, tendrás la oportunidad de investigar y monitorear cambios en normativas y políticas que puedan influir en nuestra industria, contribuyendo así a mantenernos a la vanguardia. Tu capacidad para comunicarte eficazmente será esencial, tanto para interactuar con organismos reguladores como para coordinar con diferentes áreas dentro de la empresa.

En este puesto, buscamos a una persona proactiva, con un enfoque orientado a la solución de problemas y un compromiso firme con el desarrollo profesional. Si te apasiona trabajar en un entorno estratégico que impacta directamente en la salud y el bienestar de la sociedad, este es el lugar para ti. Estamos emocionados por la posibilidad de que te unas a nuestro equipo y contribuyas a fortalecer nuestro compromiso con la calidad y la mejora continua.

Requisitos

Requisitos – Asistente de Asuntos Regulatorios

  • Estudiante universitario/a o egresado/a de las carreras de Química y Farmacia, Bioquímica, Química, Derecho o carreras afines.
  • Experiencia previa en tareas administrativas y/o gestión documental, preferentemente en industrias farmacéuticas.
  • Conocimientos básicos de registros sanitarios y normativas de DINAVISA (deseable).
  • Manejo de herramientas informáticas, especialmente Excel y Word.
  • Capacidad para organizar, controlar y dar seguimiento a documentaciones y vencimientos.
  • Atención al detalle, organización y responsabilidad. Ingles Avanzado
  • Buena comunicación y capacidad de trabajo en equipo.

Competencias valoradas

  • Organización y planificación.
  • Proactividad.
  • Capacidad de análisis.
  • Responsabilidad y confidencialidad.
  • Orientación al cumplimiento de procedimientos y normativas.

Experiencia deseable: Gestión de registros sanitarios, renovaciones, modificaciones, habilitaciones y documentación regulatoria de productos farmacéuticos.

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