**About Abbott** Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. **Working at Abbott** At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to: • Career development with an international company where you can grow the career you dream of. • We are committed to bringing the benefits of our trusted medicines to more people in the world’s fastest-growing countries. Our broad portfolio of high-quality and differentiated branded generic medicines reaches across multiple therapeutic areas including gastroenterology, women's health, cardiometabolic, pain management/central nervous system, and respiratory. • A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune. • A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. **The Opportunity** This position works out of our Tashkent location in the Established Pharmaceuticals Division. **What You’ll Do:** • Ordering of drug samples, reference standards, administrative documents, preparation of applications for registration and re-registration processes, amendments for Uzbekistan, Tajikistan and Turkmenistan; • Support in preparation of dossiers and local documents for registration and re-registration processes, amendments and submission to the Regulatory Authorities of Uzbekistan, Tajikistan and Turkmenistan; • Maintaining up-to-date data and approved documents by location, supporting the process of archiving notification letters, preparing responses to deficiency letters to the Regulatory Authorities; • Creation of purchase requests for: translation services, customs clearance of reference standards, samples of finished products of medicinal products, state duties for regulatory activities, etc.; • Processing of procedures for obtaining import authorizations for samples of finished drug products, interaction with customs broker on customs clearance issues; • Monitoring of availability / validity of GMP, CPP certificates for Uzbekistan, Tajikistan and Turkmenistan; • Collaboration with partners, support ongoing RA activities / inquiries; • Work in the company's systems. **Requirements:** • Higher education (medical, pharmaceutical, chemical or biotechnological) • Experience in a similar role from 1 year • English - intermediate, Russian - intermediate An Equal Opportunity Employer Abbot welcomes and encourages diversity in our workforce. We provide reasonable accommodation to qualified individuals with disabilities. To request accommodation, please call 224-667-4913 or email corpjat@abbott.com