제약사업부 Qa Specialist (안산)

AbbVie

Ansan, South Korea
Quality control and document management
Supplier and laboratory management
Complaint and change control handling
This position is responsible for quality control, document control, supplier management, artwork development and revision, and activities related to product release complying with Korea GMP/GIP and Abbott corporate requirements

Job Summary

  • This position is responsible for quality control, document control, supplier management, artwork development and revision, and activities related to product release complying with Korea GMP/GIP and Abbott corporate requirements.
  • The role includes managing complaint handling, change control, CAPA management, supplier audits, laboratory coordination, and training within the pharmaceutical quality assurance function.
  • The office location is Abbott warehouse in Ansan, and the position requires collaboration with multiple internal and external stakeholders to ensure product quality and regulatory compliance.

Matching Summary

This position is responsible for quality control, document control, supplier management, artwork development and revision, and activities related to product release complying with Korea GMP/GIP and Abbott corporate requirements.

Skills & Requirements

Must-have

  • Quality control and document management
  • Supplier and laboratory management
  • Complaint and change control handling
  • Artwork development and revision
  • Compliance with Korea GMP/GIP
  • Batch product release activities

Nice-to-have

  • Training coordination and matrix maintenance
  • Internal and external audit support
  • Regulatory submission support
  • Financial activities management for QA team

Key Requirements

  • Bachelor’s degree in pharmacy, chemistry, biology or related field
  • More than 3 years’ pharmaceutical QA/QC experience
  • Familiarity with Pharmaceutical Law and GMP/GIP
  • Basic English communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter