Gestión de todas las actividades regulatorias relacionadas con el ciclo de vida de los productos de la compañía. Control de las distintas fases de evaluación de la documentación, coordinando las respuestas a posibles declaraciones y ajuste del c
Como Regulatory Affairs Officer la persona deberá aportar experiencia mínima de 2 años en el departamento de registros de laboratorio de medicamentos de uso humano. Será valorada también experiencia en productos sanitarios, complementos alimenta
The Jazz mission is to bring meaningful medicines to patients with high unmet need. The field of Acute Leukaemia is a major strategic driver for Jazz with significant opportunities for CPX-351 in current and future indications, making this role criti
FUTURE TALENT PROGRAMME JUNIOR MARKETING SPECIALIST Would you like to start your career in good company? We are looking for talented and highly motivated newly graduates to join our talent
Empresa: Manpower Selección. País: España. Provincia: Madrid. Localidad: Madrid. Sector: Ingeniería y producción. Fecha: 25 de enero Requisitos: • University Degree (preferable Pharmaceutical
Main job purpose - Support the current Global Procurement Products&Services Team in Spain, also the candidate will work closely with the Regional team to promote and execute the vision and mission of Procurement in local and global category strategi
Empresa: Page Personnel. País: España. Provincia: Madrid. Sector: Sanidad, salud y servicios sociales. Fecha: 09 de enero Requisitos: *Formación universitaria en Ciencias de la Salud. *Postgrado en Regu
For our Dutch client and their growing SAP Cloud & Apps team we’re looking for (Junior/Mid-Level/Senior) SAPUI5 consultants. Job description: As a SAPUI5 consultant you are not only adding value to our customers but you also play an important role
For our Dutch client and their growing SAP Cloud & Apps team we’re looking for (Junior/Mid-Level/Senior) SAPUI5 consultants. Job description: As a SAPUI5 consultant you are not only adding value to our customers but you also play an important role
As a Regulatory Affairs Associate at PRA you will work on the preparation and review of regulatory submissions for both internal customers and external clients. Responsibilities will include: * Preparation of clinical trial submissions to support
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