Senior Scientist – Lentiviral Vector Upstream Process Development
Listed on 2026-09-12
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Research/Development
Research Scientist, Biotech Research, Pharmaceutical Science/ Research, Biotechnology
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.
- 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.
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%…
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