Manager of regulatory projects (medicinal products) in Teva

Briefly about us: Teva is a pharmaceutical company with 1,901 generic and original medicines that are used in most key therapeutic areas. We create opportunities for a better life, and in everything we do, we adhere to the highest standards of ethical business conduct and integrity. In Ukraine, Teva (Teva Ukraine LLP) unites about 0 years. Position details: Region: Kyiv Company industry: Pharmaceuticals Fluency in languages : English (above average) Type of employment: full-time, work in the office. The office is located: BC "Silver Breeze", Pavla Tychyna Ave., 1st. Responsibilities: • Evaluation of the project, critical moments during its implementation Preparation of the application and registration form;• Preparation of the administrative part of the dossier;• Coordination of the work of the project group participants;• Submission of the dossier to the DEC;• Project status monitoring and reporting;• Ensuring project implementation according to the plan;• Management of changes during the project;• Communication with CHP, laboratories and production sites; • Interaction with internal customers (logistics department, marketing department); • Entering information into databases. Requirements for the candidate: • Work experience of 3 years as a specialist / manager of drug registration in Ukraine ( personal experience of successfully submitting and completing the following types of procedures: registration, re-registration, changes);• knowledge of the English language at the upper-intermediate level;• knowledge of RA legislation of Ukraine and the EU;• highly developed sense of responsibility and attentiveness; ability to work according to standard operating procedures; high level of time management and personal discipline; • Medical, pharmaceutical or chemical education; friendly working atmosphere.