文件培训qa高级专员

AstraZeneca

Quality management system establishment
Gmp documentation auditing
Batch record issuance
Organize and establish the quality management system for new facilities, ensuring alignment with existing quality systems

Job Summary

  • Organize and establish the quality management system for new facilities, ensuring alignment with existing quality systems.
  • Manage the issuance, retrieval, archiving, and destruction of documents and records, ensuring compliance with SOPs and managing the archive room.
  • Develop and maintain employee training matrices, review training materials, guide new employee onboarding, and coordinate GMP training activities.

Matching Summary

Organize and establish the quality management system for new facilities, ensuring alignment with existing quality systems.

Skills & Requirements

Must-have

  • Quality Management System establishment
  • GMP documentation auditing
  • Batch record issuance
  • Training matrix maintenance
  • Training material review
  • SOP compliance

Nice-to-have

  • Cross-departmental coordination
  • Process optimization
  • Audit support
  • Inclusive and diverse team

Key Requirements

  • 2+ years GMP industry experience
  • 4+ years pharmaceutical industry experience preferred
  • Bachelor's degree or above in Pharmacy, Bioengineering, Pharmaceutical Engineering, Biochemistry, or related fields
  • Good English proficiency preferred

Work Rights

Not specified

Tailored Resume

Cover Letter