Site Quality Head, Texas (ad Level)

Novartis

Denton, Texas, US
Base: $138,600 - $257,400; bonus/equity: performan...
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Cgmp and regulatory compliance
Quality team leadership and development
Site startup and expansion
** Novartis is seeking a Site Quality Head for their new Radioligand Therapy manufacturing site in Denton, Texas. The role involves ensuring compliance with quality standards, leading a quality team, and establishing effective quality operations to deliver life-changing therapies. **

Job Summary

  • Shape the quality foundation for a new Radioligand Therapy manufacturing site, ensuring reliable and safe delivery of life-changing therapies.
  • Lead and develop a high-performing Quality organization, partnering with site and global stakeholders to set the standard for inspection readiness and continuous improvement.
  • Drive plant startup, expansions, and technology transfer, overseeing compliant planning, commissioning, qualification, and validation activities.

Matching Summary

Match Score: 75

** Novartis is seeking a Site Quality Head for their new Radioligand Therapy manufacturing site in Denton, Texas. The role involves ensuring compliance with quality standards, leading a quality team, and establishing effective quality operations to deliver life-changing therapies. **

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

  • cGMP and regulatory compliance
  • Quality team leadership and development
  • Site startup and expansion
  • Health authority inspection readiness
  • Deviation and CAPA management
  • Cross-functional collaboration

Nice-to-have

  • Continuous improvement methods
  • Radioligand Therapy experience
  • Risk-based decision making

Key Requirements

  • Bachelor's degree in life sciences or related scientific discipline
  • Ten years of experience in GMP pharmaceutical manufacturing
  • Three years of combined QA/QC experience
  • In-depth knowledge of cGMP and FDA/ICH regulations
  • Proven success leading health authority inspections
  • Demonstrated leadership in matrix organizations

Work Rights

Not specified

Tailored Resume

Cover Letter