Rlt Head Qa Operations Us

Novartis UK

Indianapolis, Indiana, United States
Base: $168,000.00 - $312,000.00; bonus/equity: per...
Onsite
Radioligand therapy manufacturing
Sterile and aseptic manufacturing
Quality risk management
In this senior leadership role, you’ll shape and lead end-to-end Quality Operations across our United States Radioligand Therapy manufacturing network—setting the operating model, building high-performing teams, and raising the bar for inspection readiness and compliance so life-changing cancer therapies can be delivered with confidence

Job Summary

  • In this senior leadership role, you’ll shape and lead end-to-end Quality Operations across our United States Radioligand Therapy manufacturing network—setting the operating model, building high-performing teams, and raising the bar for inspection readiness and compliance so life-changing cancer therapies can be delivered with confidence.
  • You’ll partner closely with manufacturing, supply chain, regulatory, and global quality colleagues to strengthen a culture of ownership, integrity, and continuous improvement—helping Novartis reimagine medicine at scale while ensuring every product meets the highest standards.
  • US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits.

Matching Summary

In this senior leadership role, you’ll shape and lead end-to-end Quality Operations across our United States Radioligand Therapy manufacturing network—setting the operating model, building high-performing teams, and raising the bar for inspection readiness and compliance so life-changing cancer therapies can be delivered with confidence.

Salary

Base: $168,000.00 - $312,000.00; Bonus/Equity: performance-based cash incentive and annual equity awards; Benefits: comprehensive benefits package including health, life, disability, 401(k), generous time off

Skills & Requirements

Must-have

  • Radioligand Therapy manufacturing
  • sterile and aseptic manufacturing
  • Quality risk management
  • regulatory requirements and GMP
  • inspection readiness and CAPA management

Nice-to-have

  • culture of ownership and integrity
  • continuous improvement mindset
  • collaboration and bold innovation
  • unleash their full potential

Key Requirements

  • Bachelor’s degree in a scientific discipline
  • 12+ years progressive quality experience
  • 7+ years in radiopharmaceuticals or sterile/aseptic operations
  • Working knowledge of FDA/EMA/ICH regulatory requirements
  • Proven track record of successful regulatory inspections

Work Rights

Not specified

Tailored Resume

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