Regulatory Affairs Specialist

з/п не указана

Вакансия в архиве

Работодатель, вероятно, уже нашел нужного кандидата и больше не принимает отклики на эту вакансию

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Требуемый опыт работы: 1–3 года

Полная занятость, полный день

Responsibilities:

  • Management of products registration process, renewal and variation;
  • Approval process of pharmaceutical products according to Georgian legal requirements, corporate legal and ethical norms;
  • Conducting of registration / renewal / variation process for certain part of the portfolio;
  • Quality control & certification questions of company products;
  • Products launch coordination;
  • Taking measures contributing to the protection of intellectual property rights of the company;
  • Taking part in the process of internal and external approvals (permissions) of promotional materials;
  • Cooperation with regulatory team.


Requirements:

  • Experience in Regulatory Affairs not less than 2 years;
  • Higher education (medical, pharmaceutical, regulatory);
  • Presence of scientific background (medical, pharmaceutical, regulatory);
  • Business education (preferable);
  • English language - at least Upper-intermediate and Russian language skills;
  • Pro-activity, teamwork orientation, decision making and time management skills.


Conditions:

  • Work in large international company;
  • Opportunities of career growth and professional development;
  • Additional training;
  • Compensation package.

Ключевые навыки

Regulatory affairsRegulatory Authorities relationshipsNegotiation skillsВедение переговоровTime management
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Вакансия опубликована 4 августа 2017