Site Quality Head, Florida (ad Level)

Novartis UK

Winter Park, Florida, US
Base: $138,600 - $257,400; bonus/equity: performan...
Onsite
Cgmp and fda regulations knowledge
Aseptic manufacturing experience
Quality assurance and control
This is a unique opportunity to play a critical role in the start-up and ongoing quality operations of a new RLT manufacturing site, helping ensure the delivery of life changing therapies to patients around the world

Job Summary

  • This is a unique opportunity to play a critical role in the start-up and ongoing quality operations of a new RLT manufacturing site, helping ensure the delivery of life changing therapies to patients around the world.
  • You’ll lead and develop a high-performing Quality organization, partner closely with site and global stakeholders, and set the standard for inspection readiness, robust management of product quality issues, and continuous improvement.
  • 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

This is a unique opportunity to play a critical role in the start-up and ongoing quality operations of a new RLT manufacturing site, helping ensure the delivery of life changing therapies to patients around the world.

Salary

Base: $138,600 - $257,400; 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

  • cGMP and FDA regulations knowledge
  • Aseptic manufacturing experience
  • Quality Assurance and Control
  • Health authority inspections
  • Continuous improvement methods

Nice-to-have

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

Key Requirements

  • Bachelor’s degree in life sciences
  • Ten years of GMP pharmaceutical experience
  • Three years Quality Assurance/Control experience
  • US Pharmacopeia, European Pharmacopeia standards

Work Rights

Not specified

Tailored Resume

Cover Letter