по договоренности
Опыт работы не важен

Job Responsibilities:

  • Receive, review, and evaluate medical expertise related to complaints about domestic and international medical devices
  • Review and provide guidance on all medical device reports (FDA)
  • A medical review of any relevant documents, such as clinical reviews.
  • View trend reports of complaints and adverse events
  • Organize PV training for local branch employees and contract partners
  • Act as a local contact point for inspections and inform the EMEA QPPV Office
    • Work Environment:

    • Development in an international company with a diverse product portfolio
    • Decent salary and social benefits (medical and life insurance, mobile payment), annual bonus
    • Internal and external training to enhance expertise
    • Headquarters submission and a large number of global projects
    • Gaining experience in monitoring drug safety
      • Requirements:

      • Higher education in medical sciences is preferred
      • Knowledge of EMR laws and guidelines regarding medical devices
      • Work experience in the field of safety monitoring of medical devices, communication with health authorities
      • Excellent interpersonal communication and presentation skills
      • Strong patient orientation
      • English - upper-intermediate
        • Тип занятости:

          Полная занятость, полный рабочий день, у работодателя

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