Ofertas de empleo
|
AVISO: Esta oferta no se encuentra activa.
| Oferta de Trabajo |
Código: 23999
|
Puesto: Técnico de calidad gcp |
| Función: -Assist on the review of Corporate documentation, Pharmacovigilance and Clinical Trial documentation such as protocols, IMPDs, IB, ICF, Clinical Study Reports (CSR), PSMF, DSUR, etc -Support in Policies and Procedures drafting & reviewing |
| Empresa: Bros Group
|
Nº de Plazas: 1 |
| Referencia: Bros Group |
Publicada el 8/5/2017 |
Publicada hasta el 8/8/2017 |
| Tipo de Contrato: Indefinido |
Dedicación: Jornada completa |
|
| Localidad: Madrid |
Provincia: Madrid |
Disponibilidad para viajar: No |
| Fecha de Incorporación: 01/06/2017 |
Fecha de Finalización: Indefinido |
|
| Titulación Académica |
|
Farmacia (Titulación Universitaria)
|
|
| Idiomas |
| Idioma: Inglés |
Nivel Lectura: Alto |
Nivel Escrito: Alto |
Nivel Conversación: Alto |
|
| Experiencia |
|
Bachelor's degree or equivalent
3 years relevant experience in a quality role position in the pharmaceutical industry, with preference within the biopharmaceutical industry
GCP experience (others: GVP, GLP, GMP of added value)
Knowledge of QA tools, concepts and methodologies
Demonstrated ability to work in an SME, resource and time constraint environment.
Capable to identify areas for improvement in the quality system and improvement actions
Knowledge of relevant regulatory requirements
Experience in the preparation and review of documentation (Policies and Procedures) in English to regulatory standards
Demonstrated ability to manage multiple tasks/projects/priorities and complex issues
Demonstrated attitude of reliability and attention to detail
Excellent written and verbal communication skills in English
Demonstrated professional attitude towards external and internal contacts
Proficiency in the required software and computer skills
|
|
|
|
Portal de Empleo I+D+i
