M&s-documentation/training Lead-hangzhou

Sanofi UK

Hangzhou, China
Fully remote
Gxp document management
Cgmp compliance
Annual training programs
Implement and monitor quality system for quality document/record management, Training management, ensuring effective operation and compliance to CGMP and Sanofi global requirements

Job Summary

  • Implement and monitor quality system for quality document/record management, Training management, ensuring effective operation and compliance to CGMP and Sanofi global requirements.
  • Oversee and manage the creation, revision, and obsolescence of all GxP documents, ensuring accuracy, completeness, and compliance with regulatory and company requirements.
  • Develop and implement annual training programs to ensure compliance with Good Manufacturing Practices (GMP) and other regulatory standards, evaluating effectiveness and updating materials.

Matching Summary

Implement and monitor quality system for quality document/record management, Training management, ensuring effective operation and compliance to CGMP and Sanofi global requirements.

Skills & Requirements

Must-have

  • GxP document management
  • CGMP compliance
  • annual training programs
  • regulatory requirements
  • third party management

Nice-to-have

  • data-driven decisions
  • continuous improvement initiatives
  • collaboration with departments
  • digitalization strategies

Key Requirements

  • 5 years pharmaceutical quality management experience
  • Experience in developing quality system documents
  • Experience in training program development and evaluation
  • Third party management experience

Work Rights

Not specified

Tailored Resume

Cover Letter