Regulatory Affairs Manager (medical devices)

по договоренности
Опыт от 3 до 6 лет


Our client, a leading European developer and supplier of medical devices for diagnostics, prevention of infections, hygiene and wound care, is in search of Regulatory Affairs Manager

Job Responsibilities:

  • To carry out a full cycle of registration of medical devices in Russia and the CIS in accordance with the business goals
  • Support compliance with EU trade standards and provide registration experience to ensure business growth
  • Preparation / verification of applications, specifications, technical files and other necessary documents in accordance with local requirements
  • Build professional relationships with local authorities, manufacturing plants and the global registration team
  • Monitoring local legislation and registration documents. Make the necessary changes
    • Work Environment:

    • Official employment
    • Meal and telephone compensation, voluntary health insurance, life insurance
    • Quarterly bonuses on the results of work
    • Flexible working hours for employees with young children
    • The ability to receive internal and external training
      • Requirements:

      • Higher education (pharmacology, chemistry, engineering and other life sciences)
      • Excellent knowledge of regulatory requirements for the registration of medical devices in Russia and the CIS
      • Successful experience in registration medical devices from 2 years
      • Strong leadership and communication skills
      • English - Intermediate (oral and written)
        • Тип занятости:

          Полная занятость, полный рабочий день, у работодателя

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