Site Quality Head, Florida (ad Level)

Novartis

Winter Park, Florida, United States
Base: $138,600 - $257,400 py; bonus/equity: perfor...
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Cgmp pharmaceutical manufacturing experience
Health authority inspection leadership
Site startup and technology transfer
** Novartis is seeking a Site Quality Head for their new Radioligand Therapy manufacturing site in Winter Park, Florida. The role requires extensive experience in quality assurance and compliance in a GMP pharmaceutical environment, with a focus on leading quality operations and ensuring inspection readiness. **

Job Summary

  • This role offers a unique opportunity to shape the quality foundation for a new Radioligand Therapy manufacturing site at Novartis in Winter Park, Florida.
  • The successful candidate will lead inspection readiness, manage deviations and investigations, and drive continuous improvement to ensure compliant operations.
  • Employees are eligible for a comprehensive benefits package including health, life, disability, 401(k) matching, and performance-based cash incentives.

Matching Summary

Match Score: 75

** Novartis is seeking a Site Quality Head for their new Radioligand Therapy manufacturing site in Winter Park, Florida. The role requires extensive experience in quality assurance and compliance in a GMP pharmaceutical environment, with a focus on leading quality operations and ensuring inspection readiness. **

Salary

Base: $138,600 - $257,400 per year; Bonus/Equity: Performance-based cash incentive and annual equity awards eligibility; Benefits: Comprehensive health, life, disability, 401(k), and time off package

Skills & Requirements

Must-have

  • cGMP pharmaceutical manufacturing experience
  • health authority inspection leadership
  • site startup and technology transfer
  • deviation investigation and CAPA management
  • quality team building and coaching

Nice-to-have

  • Radioligand Therapy or radiopharmaceuticals experience
  • Lean Six Sigma continuous improvement methods
  • matrix organization leadership skills
  • rapid site expansion background
  • radiation safety training knowledge

Key Requirements

  • Bachelor's degree in life sciences
  • Ten years GMP pharmaceutical manufacturing experience
  • Three years combined QA/QC experience
  • Proven success leading health authority inspections

Work Rights

Not specified

Tailored Resume

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