Associate Director, Quality Systems And Compliance

AstraZeneca

Rockville, MD, United States
Base: $129,556.80 - $194,335.20 usd annual; bonus/...
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Leadership and direction for qs/c organization
Represent qs/c on governance teams
Facilitate staff growth and development
** AstraZeneca is seeking an Associate Director of Quality Systems and Compliance for their Rockville, MD, cell therapy facility. The role involves leadership in quality assurance and compliance, ensuring that operations meet high standards to deliver life-saving therapies to patients. **

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.
  • You will represent the QS/C department and/or the Quality Organization on assigned site governance and operational teams internally, and as an empowered functional representative externally to ensure results are aligned with site business objectives.
  • The annual base pay for this position ranges from $129,556.80 - $194,335.20 USD Annual.

Matching Summary

Match Score: 75

** AstraZeneca is seeking an Associate Director of Quality Systems and Compliance for their Rockville, MD, cell therapy facility. The role involves leadership in quality assurance and compliance, ensuring that operations meet high standards to deliver life-saving therapies to patients. **

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, health benefits including medical, prescription drug, dental, and vision coverage

Skills & Requirements

Must-have

  • Leadership and direction for QS/C organization
  • Represent QS/C on governance teams
  • Facilitate staff growth and development
  • Strategic support for Quality Site Lead
  • Balance patient safety, compliance, and supply

Nice-to-have

  • Experience with Veeva Vault
  • Experience with Cell Therapy regulatory inspections
  • Engaging with global regulatory bodies

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
  • Experience in audit and inspection management
  • M.S. degree in Science, Engineering, Pharmacy, or related technical field
  • Advanced degree in Science, Engineering, Biochemistry, Pharmacy or related technical field
  • Extensive working knowledge of international Cell Therapy GxP regulatory frameworks

Work Rights

Not specified

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