Specialist I&ii, Manufacturing-lean

AstraZeneca

Suzhou, China
Deviation investigation and change control
Risk assessment and compliance
Process optimization and efficiency
Responsible for deviation investigation, change control, and risk assessment to drive continuous improvement and ensure GMP compliance within the department

Job Summary

  • Responsible for deviation investigation, change control, and risk assessment to drive continuous improvement and ensure GMP compliance within the department.
  • Analyze process flows and data to optimize production processes, standardize operations, and enhance efficiency and quality.
  • Support internal and external audits, manage SHE inspections, and oversee internal production projects, including cross-departmental collaboration.

Matching Summary

Responsible for deviation investigation, change control, and risk assessment to drive continuous improvement and ensure GMP compliance within the department.

Skills & Requirements

Must-have

  • Deviation investigation and change control
  • Risk assessment and compliance
  • Process optimization and efficiency
  • GMP compliance and documentation
  • SHE inspection and tracking

Nice-to-have

  • Team collaboration and cross-functional projects
  • Continuous improvement mindset
  • Data integrity management

Key Requirements

  • Bachelor's degree in relevant science
  • 3+ years of relevant experience
  • Experience with deviation investigation, CAPA, change control
  • Strong GMP drug manufacturing concepts
  • Proficient English communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter