Associate Director, Quality Systems And Compliance

AstraZeneca

Rockville, Maryland, US
Base: $129,556.80 - $194,335.20 usd annual; bonus/...
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Quality systems & compliance
Cell therapy manufacturing
Gxp regulatory frameworks
** AstraZeneca is seeking an Associate Director of Quality Systems and Compliance at their Rockville, Maryland facility, focusing on delivering life-saving cell therapies. The role involves providing leadership and strategic support to ensure quality and compliance objectives align with site goals. **

Job Summary

  • 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.
  • 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.
  • 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 at their Rockville, Maryland facility, focusing on delivering life-saving cell therapies. The role involves providing leadership and strategic support to ensure quality and compliance objectives align with 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, health benefits (medical, prescription drug, dental, and vision)

Skills & Requirements

Must-have

  • Quality Systems & Compliance
  • Cell Therapy Manufacturing
  • GxP Regulatory Frameworks
  • Audit and Inspection Management
  • Cross-functional Work Environment

Nice-to-have

  • Develop talent and staff
  • Strategic support for growth
  • Influence senior collaborators
  • Innovative science and technology

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 with Cell Therapy regulatory inspections
  • Extensive working knowledge of international Cell Therapy GxP regulatory frameworks

Work Rights

Not specified

Tailored Resume

Cover Letter