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No se requiere experiencia
Retribución sin especificar
Administrativos y secretariado
Empleado
1
40
Duración de la oferta: hasta el 06/08/2021.
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
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
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