Director, Sr. Global Regulatory Lead - Cardiorenal

CSL Behring

Ch, Switzerland
On-site
Global regulatory strategy development
Health authority interactions (fda, ema)
Product lifecycle management
CSL Behring is seeking a Director, Senior Global Regulatory Lead for their Cardiorenal division in Switzerland. The ideal candidate will have extensive experience in regulatory affairs within the biotech or pharmaceutical industry and will be responsible for developing global regulatory strategies, leading health authority interactions, and mentoring team members

Job Summary

  • Develops a global, integrated regulatory strategy ensuring innovative and scientifically sound regulatory approaches for assigned products, with a patient-centric focus and appropriate risk-taking to achieve successful regulatory outcomes from early development through post-marketing lifecycle activities.
  • Leads health authority interactions (FDA, EMA) and builds productive relationships to drive positive regulatory outcomes globally.
  • Applies CSL leadership capabilities and supports talent development, succession planning, and team empowerment.

Matching Summary

Match Score: 85

CSL Behring is seeking a Director, Senior Global Regulatory Lead for their Cardiorenal division in Switzerland. The ideal candidate will have extensive experience in regulatory affairs within the biotech or pharmaceutical industry and will be responsible for developing global regulatory strategies, leading health authority interactions, and mentoring team members.

Skills & Requirements

Must-have

  • Global regulatory strategy development
  • Health authority interactions (FDA, EMA)
  • Product lifecycle management
  • Cross-functional team leadership
  • Regulatory intelligence utilization

Nice-to-have

  • Patient-centric focus
  • Risk-taking for regulatory outcomes
  • Talent development and succession planning

Key Requirements

  • Bachelor’s degree in life science
  • 10+ years in biotech/pharma
  • 8+ years in regulatory affairs
  • 5+ years with developmental products
  • 5+ years leading teams
  • Knowledge of EU, US, Japan regulatory requirements
  • Direct health authority interaction experience

Work Rights

Not specified

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