Site Quality Head, Florida (ad Level)

Novartis UK

Winter Park, Florida, US
Base: $138,600 - $257,400; bonus/equity: performan...
On-site
Site quality strategy and governance
Cgmp and fda regulations knowledge
Health authority inspection leadership
Novartis UK is seeking a Site Quality Head for its new Radioligand Therapy manufacturing site in Winter Park, Florida. The ideal candidate should have extensive experience in GMP pharmaceutical environments and a strong background in Quality Assurance and Control, with leadership skills to develop a high-performance quality organization

Job Summary

  • Shape the quality foundation for a new Radioligand Therapy manufacturing site, combining rigorous compliance with strong, visible leadership.
  • Lead and develop a high-performing Quality organization, partner closely with site and global stakeholders, and set the standard for inspection readiness.
  • Drive plant startup, expansions, and technology transfer, ensuring compliant planning, commissioning, qualification, and validation activities.

Matching Summary

Match Score: 85

Novartis UK is seeking a Site Quality Head for its new Radioligand Therapy manufacturing site in Winter Park, Florida. The ideal candidate should have extensive experience in GMP pharmaceutical environments and a strong background in Quality Assurance and Control, with leadership skills to develop a high-performance quality organization.

Salary

Base: $138,600 - $257,400; Bonus/Equity: Performance-based cash incentive and potential annual equity awards; Benefits: Comprehensive benefits package including health, life, disability, 401(k) with match, generous time off

Skills & Requirements

Must-have

  • Site quality strategy and governance
  • cGMP and FDA regulations knowledge
  • Health authority inspection leadership
  • Deviation and investigation oversight
  • Continuous improvement methods

Nice-to-have

  • Radioligand Therapies experience
  • Site start-up experience
  • Radiopharmaceuticals knowledge

Key Requirements

  • Bachelor's degree in life sciences
  • Ten years of GMP pharmaceutical manufacturing experience
  • Three years in Quality Assurance/Control
  • In-depth knowledge of cGMP and US FDA regulations
  • Proven success leading health authority inspections

Work Rights

Not specified

Tailored Resume

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