Associate Director, Quality Systems And Compliance

AstraZeneca

Rockville, Maryland, USA
Base: $129,556.80 - $194,335.20 usd annual; bonus/...
Hybrid
Quality systems & compliance leadership
Cell therapy manufacturing
Audit and inspection management
As the Quality Systems & Compliance Associate Director, Cell Therapy, you will provide leadership, direction and mentoring to ensure that the QS/C organization is successful in meeting the quality and manufacturing objectives in support of site goals

Job Summary

  • As the Quality Systems & Compliance Associate Director, Cell Therapy, you will provide leadership, direction and mentoring to ensure that the QS/C organization is successful in meeting the quality and manufacturing objectives in support of site goals.
  • This manufacturing facility aims to make a direct contribution and immediate impact to patients by delivering life-saving cell therapies.
  • The annual base pay for this position ranges from $129,556.80 - $194,335.20 USD Annual.

Matching Summary

As the Quality Systems & Compliance Associate Director, Cell Therapy, you will provide leadership, direction and mentoring to ensure that the QS/C organization is successful in meeting the quality and manufacturing objectives in support of site goals.

Salary

Base: $129,556.80 - $194,335.20 USD Annual; Bonus/Equity: short-term incentive bonus opportunity, equity-based long-term incentive program; Benefits: qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage

Skills & Requirements

Must-have

  • Quality Systems & Compliance leadership
  • Cell Therapy manufacturing
  • Audit and inspection management
  • Cross-functional work environment
  • Patient safety, compliance, and supply balance

Nice-to-have

  • Develop and mentor staff
  • Strategic support for growth
  • Influence senior collaborators
  • Veeva Vault experience
  • Cell Therapy regulatory inspections

Key Requirements

  • B.S. degree in Science, Engineering, Pharmacy, or related technical field
  • Minimum of 5 years of applicable experience
  • Minimum of 2 years of management/supervisory/project management experience
  • M.S. degree in Science, Engineering, Pharmacy, or related technical field
  • Extensive working knowledge of international Cell Therapy GxP regulatory frameworks

Work Rights

Not specified

Tailored Resume

Cover Letter