Job Summary

• This position is responsible for quality control, document control, supplier management, artwork development and revision, activities related to product release, QC reagents and standard supply, complaint handling and general management activities complying with Korea GMP/GIP, applicable regulatory standards and Abbott corporate requirements.
• Core responsibilities include product batch release, complaint management, change control, nonconformance and CAPA management, artwork management, internal and external audit/inspection, supplier management, laboratory management, and document management.
• The role requires a Bachelor’s degree or equivalent in pharmacy, chemistry, biology or related scientific discipline with more than 3 years’ experience in pharmaceutical quality assurance or quality control, and familiarity with Pharmaceutical Law and related regulations and GMP/GIP knowledge.

Matching Summary

Skills & Requirements

Key Requirements

• Bachelor’s degree or equivalent
• More than 3 years’ experience
• Familiarity with Pharmaceutical Law and regulations
• GMP/GIP knowledge
• Proficiency in MS Office
• Basic English Communication Skills

Work Rights