Associate Director, Quality Management – Translational Medicine Oncology

Vacancyz

Base: $137,344.80 - $206,017.20; bonus/equity: sho...
Not specified
Bachelor's degree in sciences
5+ years pharmaceutical qa experience
Knowledge of ich-gcp regulations
The Associate Director of Quality Management in Translational Medicine Oncology at AstraZeneca is a pivotal role aimed at ensuring quality across the Translational Medicine and Biomarker Science & Technology organizations. The ideal candidate will have extensive experience in quality assurance within the pharmaceutical or biotech industries, particularly in clinical research and biomarker development. This position offers competitive compensation and a commitment to diversity and inclusion in the workplace

Job Summary

  • This role drives quality excellence across Translational Medicine and Biomarker Science organizations to deliver high-quality science to patients.
  • The incumbent will advise on compliance, lead continuous improvement initiatives, and manage risk identification and CAPA effectiveness.
  • The position offers a competitive total reward program including a market-driven base salary, bonus, long-term incentives, and comprehensive benefits.

Matching Summary

Match Score: 85

The Associate Director of Quality Management in Translational Medicine Oncology at AstraZeneca is a pivotal role aimed at ensuring quality across the Translational Medicine and Biomarker Science & Technology organizations. The ideal candidate will have extensive experience in quality assurance within the pharmaceutical or biotech industries, particularly in clinical research and biomarker development. This position offers competitive compensation and a commitment to diversity and inclusion in the workplace.

Salary

Base: $137,344.80 - $206,017.20; Bonus/Equity: Short-term incentive bonuses and equity-based awards available; Benefits: Qualified retirement programs, paid time off, health, dental, and vision coverage

Skills & Requirements

Must-have

  • Bachelor's degree in sciences
  • 5+ years pharmaceutical QA experience
  • Knowledge of ICH-GCP regulations

Nice-to-have

  • Master's degree in biology or chemistry
  • Experience with Veeva QMS digital systems
  • Track record leading cross-functional projects

Key Requirements

  • Bachelor's degree in sciences required
  • 5+ years relevant work experience
  • Significant pharma/biotech QA background

Work Rights

Not specified

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