Associate Director Development Quality

AstraZeneca

NC, United States
Cgmp standards into practice
Qa oversight of manufacturing documentation
Release internal drug substance
Join AstraZeneca as a Lead Quality Advisor, Site Quality (Development Quality) to provide GMP leadership across our development value chain

Job Summary

  • Join AstraZeneca as a Lead Quality Advisor, Site Quality (Development Quality) to provide GMP leadership across our development value chain.
  • In this high‑influence role, you will build and translate robust, risk‑based cGMP standards into practice across Development.
  • Help us compose standards that safeguard patients and enable life‑changing medicines worldwide.

Matching Summary

Join AstraZeneca as a Lead Quality Advisor, Site Quality (Development Quality) to provide GMP leadership across our development value chain.

Skills & Requirements

Must-have

  • cGMP standards into practice
  • QA oversight of manufacturing documentation
  • Release internal Drug Substance
  • Lead regulatory inspections
  • Approve equipment/facilities documentation
  • continuous improvement, lean ways of working

Nice-to-have

  • influential communication across interfaces
  • Credibility in the QA community
  • drive for excellence
  • Excellent team working and networking skills
  • Demands excellence and delivers

Key Requirements

  • Science degree with extensive experience
  • 5–10+ years in pharmaceutical GMP
  • Deep QA expertise in Quality Systems
  • BS degree with extensive experience
  • 5-10 years of working within pharmaceutical GMP

Work Rights

Not specified

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