Abbott

JOB DESCRIPTION:

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 
• Experience in a similar role from 1 year
• English - intermediate, Russian - pre-intermediate

The base pay for this position is

N/A

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:

Regulatory Operations

DIVISION:

EPD Established Pharma

LOCATION:

Uzbekistan > Tashkent : Oybek St., 38a

ADDITIONAL LOCATIONS:

WORK SHIFT:

Standard

TRAVEL:

MEDICAL SURVEILLANCE:

SIGNIFICANT WORK ACTIVITIES: