Scientist, Analytical Development - Malvern, United States - Disability Solutions

Description

Johnson & Johnson is recruiting for a Scientist, Analytical Development located in Malvern, PA.

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 .

The Biotherapeutics Development-Analytical Development (BioTD-AD) group is seeking an energetic, and highly motivated Scientist to support CAR-T cell therapies. The individual will be a point of contact person overseeing the development of test methods (flow cytometry, cell count, and/or potency) for in-process and release assays to support Janssen's CAR-T drug development and production, and support the end-to-end automation of these methods. The Scientist will have the opportunity to engage in multi-functional teams. They will learn from and contribute to industry-leading drug discovery/development programs that has brought numerous quality therapeutics to patients and has made significant contributions to human health.

Key Responsibilities:

• Serve as an analytical technical expert for method development to support CAR-T cell therapy products.
• Lead method development and optimization of analytical methods to ensure robust assay performance.
• Provide technical support for troubleshooting and share knowledge/experience with team members.
• Engage and/or lead technical investigation strategies in support of product investigations with respect to clinical outcomes or adverse events driving to root cause.
• Effectively communicate scientific data and results across technical teams, project teams, and to the health authority as needed.
• Collaborate with QA and regulatory agencies during audits.
• Work in a team environment as well as contributing individually to meet project timelines and objectives.