Downstream Scientist, Viral Vector Process Development

genscript; United States; On-site; USD 120,000 - 160,000; Full time

Benefits offered by this job

Medical insurance

401(k) plan

Paid parental leave

PTO & holidays

Job summary

GenScript USA Inc./ProBio Inc. is seeking a qualified scientific professional to translate research processes into GMP-compliant manufacturing for viral vectors. You will develop, scale-up, and evaluate technology transfer of LVV and AAV processes, with potential to lead a small team.

The ideal candidate holds a Master's or PhD with 5+ years in biotech development, excels in DOE and data analysis, and collaborates across analytical, manufacturing, QA, and regulatory teams to advance projects.

Qualifications

• Master's or PhD with 5+ years in biotech/viral vector development.
• Experience with LVV and AAV process development.
• Strong DOE and statistical analysis skills.
• Regulatory affairs experience with FDA/EMA is a plus.
• Excellent documentation and collaboration skills.

Responsibilities

• Develop and optimize downstream unit operations for viral vector manufacturing.
• Plan and perform AAV/LVV purification experiments and data reporting.
• Collaborate with internal/external partners to evaluate new bioprocessing tech.
• Support cGMP transfer, risk evaluation, and deviations.
• Prepare CMC sections for regulatory submissions.
• Present progress to management and read current literature for ideas.

Skills

DOE

Statistical analysis

Scientific communication

Project coordination

Education

Master's degree in Chemical/Biochemical Engineering

Ph.D. in related field

Tools

LVV purification techniques

Job description

GenScript USA Inc./ProBio Inc. is seeking a qualified scientific professional to translate research processes into GMP-compliant manufacturing for viral vectors. You will develop, scale-up, and evaluate technology transfer of LVV and AAV processes, with potential to lead a small team.

The ideal candidate holds a Master's or PhD with 5+ years in biotech development, excels in DOE and data analysis, and collaborates across analytical, manufacturing, QA, and regulatory teams to advance projects.