Site Quality Head, Florida (ad Level)

Novartis

Winter Park, Florida, US
Base: $138,600 - $257,400; bonus/equity: performan...
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Site quality strategy and governance
Gmp pharmaceutical manufacturing experience
Cgmp and fda regulations knowledge
** Novartis is seeking a Site Quality Head for their new Radioligand Therapy manufacturing site in Winter Park, Florida. This leadership role involves shaping the quality operations and ensuring compliance with regulatory standards while building a high-performing Quality team. **

Job Summary

  • Shape the quality foundation for a new Radioligand Therapy manufacturing site, combining rigorous compliance with strong leadership.
  • Lead and develop a high-performing Quality organization, partnering with site and global stakeholders to ensure reliable and safe delivery of life-changing therapies.
  • Oversee deviations, investigations, and corrective actions, while defining and monitoring site quality performance indicators for continuous improvement.

Matching Summary

Match Score: 75

** Novartis is seeking a Site Quality Head for their new Radioligand Therapy manufacturing site in Winter Park, Florida. This leadership role involves shaping the quality operations and ensuring compliance with regulatory standards while building a high-performing Quality team. **

Salary

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

Skills & Requirements

Must-have

  • Site quality strategy and governance
  • GMP pharmaceutical manufacturing experience
  • cGMP and FDA regulations knowledge
  • Health authority inspection leadership
  • Continuous improvement methods

Nice-to-have

  • Site start-up experience
  • Radioligand Therapies experience
  • Radiopharmaceuticals knowledge
  • Radiation safety training

Key Requirements

  • Bachelor’s degree in life sciences or related scientific discipline
  • Ten years of experience in GMP pharmaceutical manufacturing
  • Three years of experience in Quality Assurance/Control
  • In-depth knowledge of cGMP, FDA, and ICH regulations
  • Proven success leading health authority inspections

Work Rights

Not specified

Tailored Resume

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