Senior Scientist, Viral Vector Process Development, Upstream

AstraZeneca

Gaithersburg, MD, USA
Base: $108,473.60 - $162,710.40; bonus/equity: sho...
Not specified
Suspension cell culture experience
Lentiviral vector process development
Bioreactor operations and scale-up
AstraZeneca is seeking a Senior Scientist for Viral Vector Process Development, focusing on upstream processes for Lentiviral Vector production. The role requires expertise in bioreactor operations, process characterization, and cross-functional collaboration to advance cell therapy modalities. ###

Job Summary

  • The role involves building and leading a high-performing team to accelerate AstraZeneca's emerging Cell Therapy modalities portfolio.
  • Candidates will design, execute, and optimize upstream Lentiviral Vector processes with a primary focus on suspension bioreactor platforms at clinical and commercial scales.
  • The position offers a competitive annual base pay ranging from $108,473.60 to $162,710.40 along with short-term incentives and equity-based long-term programs.

Matching Summary

Match Score: 85

AstraZeneca is seeking a Senior Scientist for Viral Vector Process Development, focusing on upstream processes for Lentiviral Vector production. The role requires expertise in bioreactor operations, process characterization, and cross-functional collaboration to advance cell therapy modalities. ###

Salary

Base: $108,473.60 - $162,710.40; Bonus/Equity: Short-term incentive bonus and equity-based long-term incentive program available; Benefits: 401(k), paid vacation/holidays, health/dental/vision coverage

Skills & Requirements

Must-have

  • Suspension cell culture experience
  • Lentiviral Vector process development
  • Bioreactor operations and scale-up
  • Statistical DOE and data analysis
  • GMP documentation and compliance

Nice-to-have

  • Lean practices implementation
  • Cross-functional team collaboration
  • Single use system proficiency
  • Process automation and PAT
  • Continuous improvement mindset

Key Requirements

  • Ph.D. in Chemical/Biochemical Engineering or related field
  • 1+ years industry experience with Ph.D. or equivalent MS/BS years
  • Hands-on experience developing suspension-based LVV upstream processes
  • Experience supporting cGMP interfaces and technical transfers

Work Rights

Not specified

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