по договоренности
Опыт работы не важен

Job Responsibilities:

  • File, maintain and organise local registration submissions and maintain regulatory flags in local ERP system.
  • Provide maturity and significant RA experience for the EMEA regulatory team to accelerate market access.
  • Build, implement and maintain effective local product registration processes.
  • Reviews product change notifications issued by international manufacturing sites.
  • Monitor regulatory changes across Russia & KZ and escalate to RA leadership as necessary.
  • Provide support to the local Russian RAQA team and EMEA Regulatory team on various activities as appropriate.
    • Work Environment:

    • Development in an international company with innovative products
    • A decent level of salary and an social package (medical and life insurance, meal compensation, mobile compemsation), annual bonus
    • Internal and external training to increase the level of expertise
      • Requirements:

      • Minimum of 1,5-2 years in an RA role
      • Sound knowledge of European / Russian medical device regulatory frameworks.
      • High level communication skills.
      • Well established communications with key stakeholders.
      • Capable of leading complex projects autonomously (problem solving oriented).
      • Upper-intermediate in English
        • Тип занятости:

          Полная занятость, полный рабочий день, у работодателя

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