Senior Lentivirus Upstream Process Lead

Legend Biotech US

New Jersey

On-site

USD 127,313 - 167,099

Full time

14 days+

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Benefits offered by this job

Medical, dental, vision insurance
401(k) employer match
Paid parental leave (8 weeks)

Job summary

Legend Biotech US in Somerset, NJ seeks a Senior Scientist for Lentivirus Upstream Processing. You will design and optimize upstream production, including seed train expansion, HEK293/HEK293T culture, and bioreactor scale-up to deliver high-titer, GMP-ready vectors for clinical programs.

Requirements include an advanced degree (PhD preferred) and 5–8 years (PhD) or 8+ years (MS) in biotech; GMP experience; strong cross-functional collaboration and documentation skills to support tech transfer

Qualifications

  • Advanced degree required in a related field (PhD preferred).
  • Experience in process development or manufacturing within biotech/pharma.
  • Hands-on mammalian cell culture with HEK293/HEK293T for viral vectors.

Responsibilities

  • Design and execute upstream strategies for lentiviral vector production.
  • Optimize seed train expansion and transient transfection to improve titer.
  • Support scale-up/scale-down models and tech transfer to GMP manufacture.
  • Collaborate with CMC, Analytical Development, and Downstream teams to ensure alignment.
  • Document protocols, QC/assay parameters, and regulatory sections as needed.

Skills

Mammalian cell culture
Seed train expansion
Transient transfection
Bioreactor scale-up
GMP/CMC knowledge
Process development
Data analysis
Cross-functional collaboration

Education

PhD in Chemical Engineering/Bioengineering

Job description

Legend Biotech US in Somerset, NJ seeks a Senior Scientist for Lentivirus Upstream Processing. You will design and optimize upstream production, including seed train expansion, HEK293/HEK293T culture, and bioreactor scale-up to deliver high-titer, GMP-ready vectors for clinical programs.

Requirements include an advanced degree (PhD preferred) and 5–8 years (PhD) or 8+ years (MS) in biotech; GMP experience; strong cross-functional collaboration and documentation skills to support tech transfer

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