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

AstraZeneca

Rockville, MD, United States
Base: $103,286.40 - $154,929.60; bonus/equity: eli...
On-site
Cell therapy manufacturing support
Process development and manufacturing experience
Gmp environments
AstraZeneca is seeking a Senior Process Engineer for its Manufacturing Sciences & Technology (MS&T) team at the Rockville, MD location, focusing on the manufacturing of cell therapy products. The ideal candidate will have extensive hands-on experience in cell therapy operations, process validation, and technology transfer, with responsibilities including technical support, data analysis, and compliance with regulatory standards

Job Summary

  • This position focuses on ensuring robust, compliant, and cost-effective manufacturing of clinical and commercial cell therapy products.
  • Responsibilities include leading on-the-floor / hands-on technical support, developing technical instructions, performing data analysis, and leading complex deviation investigations.
  • The role involves supporting technology transfers, clinical manufacturing, site readiness, process validation, commercial manufacture readiness, and product lifecycle management activities.

Matching Summary

Match Score: 85

AstraZeneca is seeking a Senior Process Engineer for its Manufacturing Sciences & Technology (MS&T) team at the Rockville, MD location, focusing on the manufacturing of cell therapy products. The ideal candidate will have extensive hands-on experience in cell therapy operations, process validation, and technology transfer, with responsibilities including technical support, data analysis, and compliance with regulatory standards.

Salary

Base: $103,286.40 - $154,929.60; Bonus/Equity: eligibility for short-term incentive bonuses and equity-based awards; Benefits: qualified retirement programs, paid time off, health, dental, and vision coverage

Skills & Requirements

Must-have

  • Cell therapy manufacturing support
  • Process development and manufacturing experience
  • GMP environments
  • Data trending and analysis
  • Deviation and CAPA investigations
  • Continuous improvement initiatives
  • Technical writing and communication

Nice-to-have

  • Late-stage clinical manufacturing support
  • Process validation and commercial readiness
  • Collaboration with global functions
  • On-call rotation

Key Requirements

  • B.S. with 8+ years of hands-on industry experience
  • M.S. with 5+ years of hands-on industry experience
  • PhD with 1+ years of industry experience
  • Proficiency with statistical analysis
  • Strong data analysis and problem-solving skills

Work Rights

Not specified

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