Administrativo Departamento de Calidad (H/M) Madrid

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Administrativo Departamento de Calidad (H/M) Madrid


  • Madrid
  • Inscripción cerrada
  • 40 inscritos
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Jornada sin especificar - Contrato sin especificar - Retribución sin especificar - No se requiere experiencia

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Empresa

Manpower España

Descripción de la oferta

Descripción de la oferta

Duración de la oferta: hasta el 06/08/2021

Funciones

We are looking for an Administrative Quality Department (F/M)) for an important company in the pharmaceutical sector. If you have experience in the position, this is your opportunity !!!
Essential requirements
-Excellent written and oral English communication skills
-Understanding the linkages in quality and regulatory compliance in delivery to customer and health authority
-Strong collaboration and communication skills as well as ability to build partnerships internally and externally
-Detailed oriented, Organized and tidy
Academic Training and Knowledge
-Knowledge of ISO 9001:2015 Standard, process Excellence experience with ISO 13485 or equivalent quality standards and J&J Quality & Compliance standards
-Knowledge of Medical Device regulations
-Bachelors or Master degree in Pharma, Bioscience or Engineering with relevant experience and background in Quality area.
Experience
One year working experience in a vigilance, regulatory affairs and/or quality departments within an International Medical Device Company
MAIN FUNCTIONS
-To support BQ Lead on Recalls and/or Field Safety Corrective Actions management, and To coordinate the Recalls and/or Field Safety Corrective Actions with affected Business Units
-To support BQ Lead on complaints report to manage local vigilance system and to supervise product complaints management and notification to manufacturers
-To support BQ Lead in Stop shipment.
-Support BQ Lead to keep update the database of Quality agreements and contracts with the franchises
-Support BQ Lead to keep updated change control date base evidences.
Essential requirements
-Excellent written and oral English communication skills
-Understanding the linkages in quality and regulatory compliance in delivery to customer and health authority
-Strong collaboration and communication skills as well as ability to build partnerships internally and externally
-Detailed oriented, Organized and tidy
Academic Training and Knowledge
-Knowledge of ISO 9001:2015 Standard, process Excellence experience with ISO 13485 or equivalent quality standards and J&J Quality & Compliance standards
-Knowledge of Medical Device regulations
-Bachelors or Master degree in Pharma, Bioscience or Engineering with relevant experience and background in Quality area.
Experience
-One year working experience in a vigilance, regulatory affairs and/or quality departments within an International Medical Device Company.
It offers:
-Salary: 20.000€ gross / year.
-Contract until January 15 2022

Requisitos

Essential requirements
-Excellent written and oral English communication skills
-Understanding the linkages in quality and regulatory compliance in delivery to customer and health authority
-Strong collaboration and communication skills as well as ability to build partnerships internally and externally
-Detailed oriented, Organized and tidy
Academic Training and Knowledge
-Knowledge of ISO 9001:2015 Standard, process Excellence experience with ISO 13485 or equivalent quality standards and J&J Quality & Compliance standards
-Knowledge of Medical Device regulations
-Bachelors or Master degree in Pharma, Bioscience or Engineering with relevant experience and background in Quality area.
Experience
One year working experience in a vigilance, regulatory affairs and/or quality departments within an International Medical Device Company
  • Área

    Administrativos y secretariado

  • Categoría o nivel

    Empleados

  • Nº Vacantes

    1

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