Experienced Scientist, In-vivo CAR-T

• 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

• 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

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.

• Formulation Development
• Viral Vector Drug Product Development
• GxP Compliance
• Data Analysis and Interpretation
• Technology Transfer

• Formulation Design
• Process Scale-Up
• Statistical Analysis
• Troubleshooting
• Process Validation
• Manufacturing Support
• Experimental Documentation
• Characterization Techniques
• Data Integrity
• Problem-Solving

• Clear Communication
• Detail-Oriented
• Proactive Approach
• Cross-Functional Collaboration
• Ability to Manage Priorities

• Life Sciences
• Chemical Engineering
• Advanced Therapies
• Viral-Vector Platforms
• Commercial Readiness
• Early-Stage Development
• Late-Stage Development
• Manufacturing Readiness
• Matrixed Environment
• Continuous Process Improvement