Experienced Scientist, In-vivo CAR-T

Johnson & Johnson

Experienced Scientist developing lentiviral-vector drug product formulations for Johnson & Johnson’s healthcare innovation business. Supporting laboratory research, scale-up, technology transfer, and GMP-ready manufacturing processes.

Posted 8/13/2026full-timeSpring House • Pennsylvania • 🇺🇸 United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in formulation development and optimization of viral vector drug products, with a strong focus on data analysis, technology transfer, and compliance with GxP principles. Proven ability to collaborate effectively in cross-functional teams while managing multiple priorities in dynamic environments.

Highest-signal resume keywords

Formulation DevelopmentViral Vector Drug Product DevelopmentGxP ComplianceData Analysis and InterpretationTechnology Transfer

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Formulation DesignProcess Scale-UpStatistical AnalysisTroubleshootingProcess ValidationManufacturing SupportExperimental DocumentationCharacterization TechniquesData IntegrityProblem-Solving

Soft Skills

Clear CommunicationDetail-OrientedProactive ApproachCross-Functional CollaborationAbility to Manage Priorities

Industry Keywords

Life SciencesChemical EngineeringAdvanced TherapiesViral-Vector PlatformsCommercial ReadinessEarly-Stage DevelopmentLate-Stage DevelopmentManufacturing ReadinessMatrixed EnvironmentContinuous Process Improvement

About the role

Key responsibilities & impact

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

Requirements

What you’ll need

B.S. or M.S. with 2–4 years of experience in an appropriate scientific discipline, such as Life Sciences or Chemical Engineering
Relevant experience in formulation development of viral vectors and/or advanced therapies
Strong hands-on laboratory experience in viral-vector drug-product development and statistics
Understanding of process scale-up, technology transfer, and GxP principles
Strong scientific problem-solving and data interpretation skills
Hands-on, proactive, and detail-oriented approach
Ability to work effectively in a cross-functional, matrixed environment
Clear and concise written and verbal communication skills
Ability to manage multiple priorities in a dynamic development environment
Preferred: experience with viral-vector platforms, particularly LVV, and/or advanced therapies
Preferred: familiarity with formulation implementation for early- and late-stage development, process validation, and manufacturing support
Preferred: exposure to early- and late-stage development requirements or commercial readiness activities

Benefits

Comp & perks

Inclusive work environment
Interview process accommodations for applicants with disabilities
Equal opportunity employment