რეგისტრაციის სპეციალისტი

We're looking for a part-time Registration Specialist for one of the largest pharmaceutical manufacturer's representation in Tbilisi. Key Responsibilities: Manage the full lifecycle of pharmaceutical product registration, variation submissions, and re-registration activities. Prepare, review, and submit regulatory dossiers in accordance with local legislation and regulatory requirements. Liaise with health authorities and ensure compliance with regulatory requirements Monitor changes in regulatory legislation and ensure company compliance Coordinate with internal departments (Medical, Marketing, Supply Chain) and external partners Maintain regulatory documentation and databases Support product launches by ensuring timely approvals Track registration timelines and proactively address regulatory issues and requests. Required Criteria: Bachelor's Degree (Medical or Pharmaceutical) 2-3 years of working experience as a regulatory affairs specialist/registration specialist Knowledge of either English or Russian language Additional Information: Schedule - part-time, flexible (22 working hours weekly) Location: Remote Medical Insurance; Fuel limit - 80 liters interested in this opportunity? Please, send your resume: [email protected]