Downstream Scientist, Viral Vector Process Development
genscript
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Benefits offered by this job
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
Education
Tools
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.
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