Regulatory affairs specialist junior

  • Azienda:

    Cosmo Intelligent Medical Devices

  • Località:

    Rome, Italy

Cosmo IMD has developed in recent years unrivaled expertise in multiple aspects related to the AI Med Tech business, such as medical device Hardware and Software design, healthcare Artificial Intelligence development, medical data harvesting, clinical development, scientific production, and regulatory expertise in the US and worldwide. […]
Key Responsibilities:Assess, prepare, and manage technical documentation to support certification and submission processes in the European Union and U. S. A. Prepare and manage technical dossiers for submission in other countries according to local regulations...

10 giorni fa da: it.lifeworq.com

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