Senior Scientist, Viral Vector Downstream - Process Development

Peptide Atlas

Northern (KY)

Hybrid

USD 120,000 - 180,000

Full time

4 days ago
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Benefits offered by this job

Medical, dental, and vision insurance
401(k) with company match
Paid parental leave
Generous paid time off

Job summary

GenScript USA Inc./ProBio Inc. is seeking a bench-focused scientist to translate research processes to GMP manufacturing for LVV and AAV viral vectors.

You will develop, scale-up, and transfer processes, potentially leading a small team, and collaborate across QA, QC, MFG, and analytics to ensure successful technology transfer and regulatory readiness. The role requires a PhD or Master’s with 5+ years of biotech experience, strong DOE/statistics skills, and the ability to work independently in a

Qualifications

  • Master’s or Ph.D. degree with 5+ years’ industry experience in Chemical/Biochemical Engineering, Biological Sciences, or a related scientific discipline in biotech development with LVV and AAV process experience a plus.
  • Experience with viral vector process development and manufacturing is highly preferred.
  • Strong understanding of process scale-up and scale-down modeling.
  • Experience with CMC regulatory affairs for FDA/EMA is a plus.
  • Strong organizational and detailed documentation abilities are required.
  • Ability to work independently in hands-on lab setting and learn new techniques.
  • Excellent interpersonal, verbal, and written communication skills.

Responsibilities

  • Hands-on development and optimization of downstream unit operations for viral vector manufacturing.
  • Plan/design/execute AAV/LVV purification experiments and report data summaries.
  • Collaborate with internal/external partners to evaluate new bioprocessing technologies.
  • Support technology transfer, cGMP risk evaluation, and deviation management with cross-functional teams.
  • Maintain detailed project timelines and documentation.
  • Prepare CMC sections for regulatory submissions (IND, Annual Reports, BLA).
  • Present updates to management on process development and manufacturing support.
  • Review literature to inform process design and development.

Skills

DOE knowledge
Statistical analysis
Independent work
Strong communication
Collaboration and teamwork

Education

Master’s or Ph.D. in Chemical/Biochemical Engineering or Biological Sciences

Job description

GenScript USA Inc./ProBio Inc. is seeking a bench-focused scientist to translate research processes to GMP manufacturing for LVV and AAV viral vectors.

You will develop, scale-up, and transfer processes, potentially leading a small team, and collaborate across QA, QC, MFG, and analytics to ensure successful technology transfer and regulatory readiness. The role requires a PhD or Master’s with 5+ years of biotech experience, strong DOE/statistics skills, and the ability to work independently in a

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