Обязанности:
International Pharmaceutical Company Responsibilities Registration of medicinal products. Ensuring the translation of documentation necessary for the submission of dossiers to regulatory authorities. Writing drafts of ND (normative documentation) and PIL, preparation of pack artworks with relevant department. Execution of documents for payment of state duty. Preparation of an electronic application in the required format. Submission of documents to regulatory authorities. Interaction with experts (correspondence by e-mail, telephone conversations). Tracking the status of electronic application. Amendment of documents in accordance with the recommendations of regulatory authorities. Regular information the management about the stages of registration and changes required. Tracking the correctness of the information entered in the State Register of Medicines. Qualification & experience: High pharmaceutical, chemical biological, or medical education. 2+ year of similar experience in reputed pharmaceutical company. Knowledge of Russian Regulation in the field of medicines circulation. Fluency in English (business correspondence, communications &presentations). Personal computer skills (MS Office). Сonditions can be discussed.Похожие вакансии
Менеджер по регистрациии биологических препаратов / Drug regulatory affairs manager
Договорная
Москва
Р-Фарм