Experienced Scientist, In-vivo CAR-T

Johnson & Johnson Innovative Medicine

1d • Onsite

About The Position

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. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com. As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

The Experienced Scientist will support the formulation development, optimization, and scale-up of lentiviral vector (LVV) drug product formulation early to late-stage development. The role combines hands-on laboratory work with strong cross-functional collaboration to ensure robust, scalable, and GMP-ready processes.

Requirements

• B.S. or M.S. with 2-4 years of experience in an appropriate scientific discipline (Life Sciences or Chemical Engineering) is required
• Relevant experience in formulation development of viral vectors and/or advance therapies
• Strong hands-on laboratory experience in drug product development of viral vector 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 communication skills (written and verbal)
• Ability to manage multiple priorities in a dynamic development environment

Nice To Haves

• Experience with viral vector platforms, LVV in particular, and/or advanced therapies
• Familiarity with formulation implementation for both early and late-stage development, process validation (e.g., LCPV) and manufacturing support
• Exposure to both early and late-stage development requirements or commercial readiness activities

Responsibilities

• Formulation development and optimization of viral vectors e.g., 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, optimization, and decision-making
• Support formulation robustness activities
• Contribute to scale-up and manufacturing readiness, including support of technology transfer to internal sites or CMOs
• Collaborate cross-functionally with Analytical Development, Statistical, API, MSAT, Quality, Manufacturing, and Regulatory teams to ensure alignment on formulation strategy and execution of viral vectors
• Document experimental work and results in accordance with GxP and data integrity requirements
• Participate in troubleshooting activities and continuous process improvement initiatives

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree