Senior Scientist, Viral Vector Process Development, Upstream

AstraZeneca

Gaithersburg, MD, US
Base: $108,473.60 - $162,710.40; bonus/equity: sho...
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Lentiviral vector (lvv) processes
Suspension bioreactor platforms
Process characterization
** AstraZeneca is seeking a Senior Scientist for Viral Vector Process Development in Gaithersburg, MD, who will focus on optimizing and scaling up upstream Lentiviral Vector processes. The ideal candidate will possess hands-on experience in bioprocessing and a strong collaborative spirit to work within cross-functional teams. **

Job Summary

  • The candidate will play a critical role in building and leading a high-performing team that accelerates AstraZeneca’s emerging Cell Therapy modalities portfolio.
  • You will design, execute, and optimize upstream Lentiviral Vector (LVV) processes with a primary focus on suspension bioreactor platforms at clinical and commercial scales.
  • The annual base pay for this position ranges from $108,473.60 - $162,710.40.

Matching Summary

Match Score: 75

** AstraZeneca is seeking a Senior Scientist for Viral Vector Process Development in Gaithersburg, MD, who will focus on optimizing and scaling up upstream Lentiviral Vector processes. The ideal candidate will possess hands-on experience in bioprocessing and a strong collaborative spirit to work within cross-functional teams. **

Salary

Base: $108,473.60 - $162,710.40; 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

Skills & Requirements

Must-have

  • Lentiviral Vector (LVV) processes
  • suspension bioreactor platforms
  • process characterization
  • scale-up/tech transfer
  • suspension cell culture
  • media/feed optimization

Nice-to-have

  • Lean practices and digital tools
  • cross-functional collaboration
  • problem solving and troubleshooting
  • continuous improvement
  • regulatory filings

Key Requirements

  • Ph.D. with 1+ years industry experience
  • M.S. with 4+ years industry experience
  • B.S. with 5+ years industry experience
  • Hands on experience developing suspension-based LVV upstream processes
  • Familiarity with clinical/commercial scale considerations
  • Experience supporting cGMP interfaces

Work Rights

Not specified

Tailored Resume

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