Senior Scientist, LVV Formulation & Scale-Up (CAR-T)

6084-Janssen Research & Development, LLC Legal Entity

Spring House (PA)

On-site

USD 110,000 - 140,000

Full time

14 days+
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Job summary

Johnson & Johnson is seeking an Experienced Scientist, In-vivo CAR-T to advance LVV drug product formulation from early to late development. The role combines hands-on bench work with cross-functional collaboration to ensure scalable, GMP-ready processes and successful technology transfers.

Based on-site in Spring House, PA or Leiden, Netherlands, you will contribute to robust development, data interpretation, and ongoing process improvements in a dynamic, matrixed environment.

Qualifications

  • BS or MS with 2–4 years in Life Sciences or Chemical Engineering.

Responsibilities

  • Formulation development and optimization of LVV drug product across early and late development stages.
  • Perform hands-on laboratory work including formulation design, optimization, and characterization.
  • Analyze and interpret data to support formulation development and decision-making.
  • Support formulation robustness activities.
  • Contribute to scale-up and manufacturing readiness, including technology transfer to internal sites or CMOs.
  • Collaborate cross-functionally with Analytical Development, Statistical, API, MSAT, Quality, Manufacturing, and Regulatory teams.
  • Document experimental work and results in accordance with GxP and data integrity requirements.
  • Participate in troubleshooting activities and continuous process improvement initiatives.

Skills

Analytical Reasoning
Biochemistry
Chemistry
Manufacturing and Control (CMC)
Collaboration
Conducting Experiments
Data Quality
Drug Discovery Development
Molecular Diagnostics
Patent Applications
Pharmacogenetics
Report Writing
Research Documents
Scientific Research
Technologically Savvy
Written Expression

Education

BS/MS in Life Sciences or Chemical Engineering

Tools

Job description

Johnson & Johnson is seeking an Experienced Scientist, In-vivo CAR-T to advance LVV drug product formulation from early to late development. The role combines hands-on bench work with cross-functional collaboration to ensure scalable, GMP-ready processes and successful technology transfers.

Based on-site in Spring House, PA or Leiden, Netherlands, you will contribute to robust development, data interpretation, and ongoing process improvements in a dynamic, matrixed environment.

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