제약사업부 Qa Specialist (안산)

Abbott

Ansan, South Korea
Korea gmp/gip compliance
Product batch release activities
Complaint handling and investigation
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

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, artwork management, internal and external audits, supplier management, laboratory management, and document management.
  • The role requires a Bachelor’s degree in a scientific discipline, over 3 years of experience in pharmaceutical QA/QC, and familiarity with pharmaceutical regulations and GMP/GIP knowledge.

Matching 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.

Skills & Requirements

Must-have

  • Korea GMP/GIP compliance
  • Product batch release activities
  • Complaint handling and investigation
  • Change Control, NC, CAPA management
  • Artwork development and revision
  • Supplier evaluation and monitoring
  • QC reagents and standard supply

Nice-to-have

  • Anticipating medical science changes
  • Cross-functional team collaboration
  • Continuous improvement mindset

Key Requirements

  • Bachelor’s degree in pharmacy, chemistry, biology
  • More than 3 years' experience in pharmaceutical QA/QC
  • Familiarity with Pharmaceutical Law and GMP/GIP
  • Basic English Communication Skills

Work Rights

Not specified

Tailored Resume

Cover Letter