JOB DESCRIPTION:

ABOUT ABBOTT:
At Abbott, we’re dedicated to helping people live more fully, in everything we do. We’re creating the future of healthcare through life-changing technologies and products that make you healthier and stronger, quickly identify when you have a medical need, and treat conditions to help you get back to doing what you love.
With global headquarters in Chicago, USA, we serve people in more than 160 countries with leading medical devices, diagnostics, nutrition products and branded generic medicines. Our 115,000 colleagues are helping millions of people to live better and healthier, every day around the world. In South Korea, we’ve been helping people live fully for more than 30 years.

Location : 대치동 & 역삼동

JOB PURPOSE AND SCOPE:

• Responsible for the coordination and preparation of document packages for regulatory submissions. 
• Monitors and improves tracking/control systems. 
• Keeps abreast of regulatory procedures and changes. 
• May direct interaction with regulatory agencies on defined matters. 
• Ensures rapid and timely approval on medical devices and continued approved status of marketed medical devices. 
• Ensures compliance with regulations and interpretations

MAIN RESPONSIBILITIES:

     

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:

MD Medical Devices

        

LOCATION:

Korea > Seoul : SamTan Building, 421 Youngdong-daero, Gangnam-gu

     

ADDITIONAL LOCATIONS:

     

WORK SHIFT:

Standard

     

TRAVEL:

Yes, 5 % of the Time

     

MEDICAL SURVEILLANCE:

Not Applicable

     

SIGNIFICANT WORK ACTIVITIES:

Not Applicable