Site Quality Head, Texas (ad Level)

Novartis

Denton, Texas, US
Base: $138,600 - $257,400 py; bonus/equity: perfor...
Onsite
Gmp pharmaceutical manufacturing environment
Quality assurance and quality control
Health authority inspection leadership
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 per year; Bonus/Equity: Performance-based cash incentive and eligibility for annual equity awards; Benefits: Comprehensive health, life, disability benefits, 401(k) with company match, generous time off package

Skills & Requirements

Must-have

  • GMP pharmaceutical manufacturing environment
  • Quality Assurance and Quality Control
  • Health authority inspection leadership
  • Continuous improvement methods
  • Risk-based decision making
  • Inspection readiness management

Nice-to-have

  • Radioligand Therapies experience
  • Radiopharmaceuticals knowledge
  • Radiation safety training
  • Matrix organization leadership
  • Stakeholder management skills
  • Lean Six Sigma application

Key Requirements

  • Bachelor’s degree in life sciences or related discipline
  • Ten years GMP pharmaceutical manufacturing experience
  • At least three years Quality Assurance and/or Quality Control experience
  • In-depth knowledge of cGMP and FDA regulations
  • Understanding of US, European Pharmacopeia and ACS standards
  • Proven success leading health authority inspections

Work Rights

Not specified

Tailored Resume

Cover Letter