Sr. Quality System Specialist I

Haleon

Suzhou, China
Quality system management
Regulatory requirements management
Document lifecycle management
Responsible for managing reviews and quality objectives, convening quality committee meetings and tracking related measures

Job Summary

  • Responsible for managing reviews and quality objectives, convening quality committee meetings and tracking related measures.
  • Supports the quality department and quality head in daily work, and provides technical support for the electronic document management system.
  • Supports factory GMP audits and internal audits at all levels, and understands and complies with applicable quality, EHS, Haleon QMS standards and company policies.

Matching Summary

Responsible for managing reviews and quality objectives, convening quality committee meetings and tracking related measures.

Skills & Requirements

Must-have

  • Quality System Management
  • Regulatory Requirements Management
  • Document Lifecycle Management
  • QMS Risk Identification
  • CAPA Effectiveness Evaluation
  • GMP Audits Support

Nice-to-have

  • Purpose-driven culture
  • Agile performance-focused
  • Human understanding and science
  • Win as One strategy

Key Requirements

  • Bachelor's degree or above
  • 1+ year pharmaceutical industry experience
  • Familiar with national and local quality regulatory requirements
  • English spoken and reading ability as working language

Work Rights

Not specified

Tailored Resume

Cover Letter