Associate Director, Quality Assurance Support

CSL Behring

Bern, Switzerland
Cgmp quality management
Gxp records and documentation review
Quality risk assessments
CSL Behring is a global biotherapeutics leader driven by its promise to save lives, developing and delivering life-saving therapies to treat people with rare and serious medical conditions worldwide

Job Summary

  • CSL Behring is a global biotherapeutics leader driven by its promise to save lives, developing and delivering life-saving therapies to treat people with rare and serious medical conditions worldwide.
  • Responsibilities include routine and non-routine quality oversight, qualification activities, and ensuring operational quality management according to cGMP.
  • The role requires strong collaboration, communication, and influencing skills to drive quality decisions and manage complex projects and deviations.

Matching Summary

CSL Behring is a global biotherapeutics leader driven by its promise to save lives, developing and delivering life-saving therapies to treat people with rare and serious medical conditions worldwide.

Skills & Requirements

Must-have

  • cGMP quality management
  • GxP records and documentation review
  • Quality risk assessments
  • Deviation management
  • CAPA management
  • Change control management

Nice-to-have

  • Proactive QA oversight
  • Cross-functional collaboration
  • Strong influencing skills
  • Coaching and mentoring
  • Subject Matter Expert for deviations

Key Requirements

  • 8+ years of experience
  • cGMP and Compliance
  • Engineering & maintenance operations
  • Utility monitoring programs
  • Material management, warehousing & logistics
  • Quality control & analytical methods
  • Change control management
  • Deviation management
  • CAPA management

Work Rights

Not specified

Tailored Resume

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