Regulatory affairs assistant

     

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:

• Arranging/ordering the agreements with vendors/Health Authorities, Power of Attorney, other administrative documentation. 

• Arranging translations, notarizations using approved vendor. 

• Proof-reading of documentation in local language and English – agreements with vendors/Health Authorities, Power of Attorney, artworks, Methods of Quality Control, approved registration documents, regulatory documentation translations. 

• Visits to Health Authorities – support in submitting documentation. 

• Support in printing, copying, scanning of documentation, preparation of documentation for mailing. 

• Support in preparation of documentation/dossiers/files for submission to Health Authorities. 

• Support in filling and maintaining various RA tracking tables. 

• Work in corporate electronic systems. 

• Support during internal and external audits. 

Requirements:

• Higher education (pharmacy/chemistry/biology/biotechnology degree). 

• English - intermediate (verbal & written), Russian - intermediate, Uzbek - fluent.

• Soft skills: accuracy to details, multi-tasking, diligent, result-oriented, ability to perform tasks in short timelines, proactive, responsible, ability to learn fast. 

• Hard skills: advanced user MS Excel, MS Word, Adobe Acrobat, Power Point; ability to learn corporate technical systems.  

     

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:

No

     

MEDICAL SURVEILLANCE:

No

     

SIGNIFICANT WORK ACTIVITIES:

Not Applicable