Job Description

Application Due Date : ~ 15 Feb. 2012

Responsibilities

• Maintain product master file related to product registrations in compliance with regulations
• Responsible for regulatory matters related to the importation of finished goods such as expeditious submission of correct documents and, assist Regulatory Head with renewals and new product registrations
• Responsible for regulation aspects of Korean labels of imported products in cooperation
• Maintain product master file related to product registrations in compliance with regulations
• Input returned goods data into SUN and separate returned goods into re-sellable/non-sellable
• Implement GMP training to logistics vendors so they will properly manage products
• Prepare documents for audits by regulatory authorities and Bio national release test

Desired Skills & Experience - Qualifications

• University or advanced degree in Pharmacology
• Over 2 yrs experience in Quality Control/ Quality Operations part preferred
• Pharmacist license (mandatory)
• Good interpersonal relationship skill with ability to work in teams
• Moderate English skill