Обязанности: Manage the registration plan in accordance to company internal requests Responsible for new registration, amendments, re-registration, certification Research country specific regulatory requirements and business environment Communication with certification agencies and local dealers Communication with government institutes and appropriate ministries Cooperation with global RA and foreign manufacturers in frame of collecting the registration dossiers and getting information required for registration Handle the budget for registration and control the expenses Create and update electronic archives of certificates and dossiers Participate in regulatory planning – operating and strategic one Perform regulatory activities to support product circulation on the market Collaborate with operating companies and business units on corporate procedures (Cross Functional Meetings, Labeling, EAEU boards, RA Standard Procedures, EBS, Workshops ) Manage registration cases through daily management and track on-time delivery of registration projects Information support to marketing, sales, customer care and logistics departments Требования: Education at university level Experience in RA/QA Fluent English High learning ability Communication skills Условия: Medical & Life insurance Annual bonus Corporate programms (implant & orthodontics treatment)
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