Senior Process Engineer, Manufacturing, Science & Technology, Cell Therapy

AstraZeneca

Rockville, MD, US
Base: $103,286.40 to $154,929.60; bonus/equity: sh...
8+ years hands-on industry experience
Cell therapy unit operations expertise
Gmp environment and batch record execution
This role focuses on ensuring robust, compliant, and cost-effective manufacturing of clinical and commercial cell therapy products at AstraZeneca's Rockville facility

Job Summary

  • This role focuses on ensuring robust, compliant, and cost-effective manufacturing of clinical and commercial cell therapy products at AstraZeneca's Rockville facility.
  • The successful candidate will lead complex deviation investigations, drive continuous improvement through change controls, and provide on-the-floor technical support for critical campaigns.
  • The position offers a competitive base salary ranging from $103,286.40 to $154,929.60 along with eligibility for short-term incentive bonuses and equity-based awards.

Matching Summary

This role focuses on ensuring robust, compliant, and cost-effective manufacturing of clinical and commercial cell therapy products at AstraZeneca's Rockville facility.

Salary

Base: $103,286.40 to $154,929.60; Bonus/Equity: Short-term incentives and equity-based awards available; Benefits: Qualified retirement programs, paid time off, health/dental/vision coverage

Skills & Requirements

Must-have

  • 8+ years hands-on industry experience
  • Cell therapy unit operations expertise
  • GMP environment and batch record execution
  • Statistical analysis and control charts proficiency
  • Deviation investigation and CAPA leadership

Nice-to-have

  • Late-stage clinical manufacturing support
  • Process validation and commercial readiness
  • Technology transfer package development
  • Multi-functional collaboration skills
  • Electronic batch record improvements

Key Requirements

  • B.S. degree with 8+ years experience
  • M.S. degree with 5+ years experience
  • PhD in Chemical/Biochemical Engineering or related field with 1+ year experience
  • Proven GMP compliance knowledge
  • Strong technical writing abilities

Work Rights

Not specified

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