概要

• 給与

  80,000 THB ~ 90,000 THB

• 業界

  Manufacturing(Pharmaceutical/Medical Equipment)

• 仕事内容

  Key Responsibilities
  
  • Ensure adherence to applicable GMP standards and relevant regulatory requirements across all quality assurance activities
  • Perform review and approval of manufacturing documentation including batch records, production-related documents, SOPs, and quality reports
  • Lead and coordinate investigations related to quality events, including deviations, CAPA implementation, and change control activities
  • Track, evaluate, and interpret quality performance indicators to support continuous improvement initiatives
  • Serve as a technical expert in GMP compliance and provide support during regulatory audits and inspections
  • Facilitate regular quality governance meetings on a monthly basis at site level
  • Support capability building of team members and promote a strong quality-focused culture within the organization