Associate Director, Quality Assurance Support

CSL Behring

Bern, Switzerland
Cgmp quality oversight
Gxp records and documentation review
Risk assessments, non-conformances, capas
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.
  • Responsible for routine and non-routine quality oversight activities, ensuring operational quality management according to cGMP, and reviewing/approving complex GxP records and documentation.
  • CSL Behring is committed to Inclusion and Belonging, celebrating differences and creating a culture of curiosity and empathy to foster strong relationships and sustain a diverse workforce.

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 oversight
  • GxP records and documentation review
  • risk assessments, non-conformances, CAPAs
  • quality performance metrics monitoring
  • Subject Matter Expert for deviations
  • proactive QA oversight

Nice-to-have

  • strong collaboration skills
  • coaching and mentoring abilities
  • excellent communication abilities
  • strong influencing and presentation skills
  • drive improvement initiatives

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

Cover Letter