Analytical Development Analyst - Pharma Sector

Grupo Crit
Grupo Crit
València, SpainOn-siteCompetitiveAdded 6 days ago
🇪🇸 Translated from Spanish

This job was originally posted in Spanish and automatically translated to English. You'll most likely need Spanish to apply.

Job Description

Are you looking for a stable project where you can grow and build a professional career?

On behalf of Grupo Crit, we are selecting an Analytical Development Analyst to join the team of a pharmaceutical laboratory located in Valencia (Paterna).

Main responsibilities:

* Organize and prioritize daily work, reporting any deviations or incidents to the person in charge.

* Contribute to and document the development of projects and their results in reports, following the applicable SOPs.

* Perform assays according to approved protocols.

* Record all documentation associated with each analysis.
* Execute analytical development studies.
* Prepare samples for the studies.

* Stay updated and constantly review the regulatory standards applicable to the assigned projects.

* Contribute to and design best practices for the correct operation of the laboratory.

On offer:

* Permanent contract
* Full-time from Monday to Friday with rotating shifts: morning shift from 6:00 AM to 2:15 PM and afternoon shift from 1:45 PM to 10:00 PM.
* Real possibility of professional development
* Life and accident insurance
* Co-payment (voluntary) private health insurance

View original advert (Spanish)

¿Buscas un proyecto estable donde desarrollarte y hacer carrera profesional?

Desde Grupo Crit seleccionamos un/a Analista de Desarrollo Analítico para incorporarse al equipo de un laboratorio farmacéutico ubicado en Valencia (Paterna).

Responsabilidades principales:

* Organizar y priorizar el trabajo diario, reportando cualquier desviación o incidencia a la persona responsable.

* Contribuir y documentar el desarrollo de los proyectos y sus resultados en informes, siguiendo los SOPs aplicables.

* Realizar los ensayos conforme a los protocolos aprobados.

* Registrar toda la documentación asociada a cada análisis.
* Ejecutar estudios de desarrollo analítico.
* Preparar muestras para los estudios.

* Mantenerse actualizado/a y revisar constantemente la normativa regulatoria aplicable a los proyectos asignados.

* Contribuir y diseñar buenas prácticas para el correcto funcionamiento del laboratorio.

Se ofrece:

* Contrato indefinido
* Jornada completa de lunes a viernes con turnos rotativos: turno de mañana de 6h a 14:15h y turno de tarde de 13:45h a 22h.
* Posibilidad real de desarrollo profesional
* Seguro de vida y accidentes
* Copago (voluntario) seguro privado de salud

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