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Senior Scientist – Lentiviral Vector Upstream Process Development

Job in Fayetteville, Cumberland County, North Carolina, 28305, USA
Listing for: Biopharma Careers
Full Time position
Listed on 2026-09-12
Job specializations:
  • Research/Development
    Research Scientist, Biotech Research, Pharmaceutical Science/ Research, Biotechnology
Salary/Wage Range or Industry Benchmark: 110000 - 150000 USD Yearly USD 110000.00 150000.00 YEAR
Job Description & How to Apply Below

Job Function:

Discovery & Pre-Clinical/Clinical Development

Job Sub Function:

Biotherapeutics R&D

Job Category:

Scientific/Technology

All Job Posting Locations:

Spring House, Pennsylvania, United States of America

Job Description:

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Learn more at  .

We are searching for the best talent for a Senior Scientist – Lentiviral Vector Upstream Process Development to be based in Spring House, PA.

Purpose:

The Senior Scientist, Lentiviral Vector Upstream Process Development, will lead development, optimization, and characterization of scalable cell culture processes for cell therapy and CAR-T programs. This role will provide scientific leadership for early- or clinical-stage process development, with emphasis on cell culture and bioreactor execution at varying scales and data-driven process understanding, platform robustness and knowledge and optimization of upstream process technologies.

This role will also support technology transfer to Johnson & Johnson’s manufacturing sites, commercial manufacturing investigations and provide subject matter expert knowledge as part of life cycle management for cell therapy products in Johnson & Johnson’s pipeline.

You will be responsible for:
  • Design and execute upstream process development studies for lentiviral therapeutic products and provide scientific guidance.
  • Conduct cell culture experiments using shake flasks, bench-scale bioreactors, and automated high-throughput systems.
  • Contribute todevelopmentof lentiviral processes to continuously improve productivity, quality, and manufacturability.
  • Perform technology transfer to and collaborate with Johnson & Johnson’s manufacturing sites
  • Support existing and new commercial manufacturing investigations and provide subject matter expert knowledge as part of product life cycle management
  • Apply statistical experimental design, data analytics, and online monitoring and visualization tools to strengthen upstream process understanding.
  • Analyze and interpret process data using JMP,Mini Tab, Python, Spotfire, or similar platforms.
  • Evaluate emerging novel upstream technologies that improve process robustness and development efficiency.
  • Collaborate closely with downstream, analytical, formulation, modeling, automation to align study design and deliverables
  • Mentor junior scientists and provide scientific leadership across programs and cross-functional work streams.
  • Author technical reports, development summaries, scientific presentations, protocols, and regulatory-supporting documentation.
Qualifications :

Required:
  • PhD in Chemical Engineering, Biochemical Engineering, Biological Sciences, Biotechnology, or related field with 2+ years of relevant experience; ORBS or MS with 4-6 years of relevant experience.
  • Experience with process development of viral based products.
  • Experience in mammalian cell culture process development for biologics, cell and gene therapy, RNA therapeutics, or related viral vector modalities.
  • Hands-on experience with cell culture, bioreactor operation, media optimization, process monitoring, and process scale-up.
  • Strong data analysis, experimental design, and technical documentation skills.
  • Demonstrated ability to independently design, execute, interpret, and communicate complex studies.
  • Excellent written and verbal communication skills.
  • Ability to work effectively in cross-functional team environments.
  • Previous experience with technology transfer of a bioprocess to clinical or commercial GMP manufacturing is strongly preferred
  • Occasional weekend work may be required
  • Up to 10%…
Position Requirements
10+ Years work experience
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