Associate Director Quality Assurance

medizinstellenmarkt.de

Qingdao, , China
Gmp compliance management
Validation program oversight
Quality management system ownership
This role is the principal quality assurance engineer for a new pMDI manufacturing facility project in Qingdao, China, responsible for ensuring GMP compliance and operational effectiveness throughout the project lifecycle

Job Summary

  • This role is the principal quality assurance engineer for a new pMDI manufacturing facility project in Qingdao, China, responsible for ensuring GMP compliance and operational effectiveness throughout the project lifecycle.
  • The incumbent will provide quality expertise, lead validation and quality system activities, and mentor QA and engineering staff while collaborating across multiple functions to meet project milestones.
  • A strong commitment to ethical conduct, compliance with AstraZeneca policies, and fostering an inclusive and diverse team culture is emphasized.

Matching Summary

This role is the principal quality assurance engineer for a new pMDI manufacturing facility project in Qingdao, China, responsible for ensuring GMP compliance and operational effectiveness throughout the project lifecycle.

Skills & Requirements

Must-have

  • GMP compliance management
  • Validation program oversight
  • Quality management system ownership
  • Cross functional collaboration
  • Quality assurance training and mentoring
  • Regulatory compliance in China
  • Project quality support

Nice-to-have

  • Automation digital process design
  • Stakeholder influence and decision making
  • Contractor and intern supervision
  • Technical competency development
  • Ethical conduct and compliance culture

Key Requirements

  • Expert knowledge of China legislation and cGMPs
  • Experience with validation and quality systems
  • Ability to influence stakeholders
  • GMP training experience
  • Not specified work authorization

Work Rights

Not specified

Tailored Resume

Cover Letter