Senior Scientist, Viral Vector Process Development, Downstream

AstraZeneca

Gaithersburg, MD, USA
Base: $108,473.60 - $162,710.40; bonus/equity: sho...
Downstream process development for viral vectors
Scale-up and tech transfer activities
Chromatography and filtration operations
AstraZeneca is at the forefront of innovation with constant new products and launches, fostering a dynamic environment that encourages collaboration and problem-solving

Job Summary

  • AstraZeneca is at the forefront of innovation with constant new products and launches, fostering a dynamic environment that encourages collaboration and problem-solving.
  • The role involves designing, executing, and optimizing scalable Lentiviral Vector downstream purification processes with a focus on clinical and commercial scales.
  • Benefits include a qualified retirement program, paid vacation and holidays, paid leaves, and comprehensive health coverage including medical, prescription drug, dental, and vision.

Matching Summary

AstraZeneca is at the forefront of innovation with constant new products and launches, fostering a dynamic environment that encourages collaboration and problem-solving.

Salary

Base: $108,473.60 - $162,710.40; Bonus/Equity: short-term incentive bonus and equity-based long-term incentive program; Benefits: retirement plan, paid leave, health coverage

Skills & Requirements

Must-have

  • downstream process development for viral vectors
  • scale-up and tech transfer activities
  • chromatography and filtration operations
  • process characterization and DOE analysis
  • cGMP and regulatory compliance
  • cross-functional collaboration in biotech

Nice-to-have

  • experience with PAT and digital tools
  • knowledge management systems exposure
  • innovation in purification technologies
  • experience with CDMOs
  • strong problem-solving skills

Key Requirements

  • Ph.D. or M.S. or B.S. with industry experience
  • hands-on downstream process development experience
  • knowledge of viral vector impurity control
  • experience with clinical/commercial scale considerations
  • understanding of FDA/EMA gene therapy guidelines

Work Rights

Not specified

Tailored Resume

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