Christopher Larson
Cell and Gene Therapy Quality Control Executive
- Role
- Vice President Quality Control at Castle Creek Biosciences, Inc
- Location
- Philadelphia, PA, US
- LinkedIn followers
- 500 followers
About Christopher Larson
Biotech executive with responsibility for GMP regulated operations, organization building, and financial accountability. I have led organizations of scientists and Managers within oncology and cell & gene therapy with oversight of quality systems supporting programs from early clinical development through commercial lot release.While rooted in QC and analytical services, my focus extends beyond daily operations; building durable operating systems, developing leaders and aligning technical execution with regulatory risk, company growth objections and capital strategies. My experience spans assay lifecycle management, GMP facility design, quality investigations and cross-functional decision making, impacting timelines, cost and enterprise risk.
Experience
Vice President Quality Control
Jun 2025 — Present · Exton, PA, US
Responsible for cGMP QC laboratory operations in support of Castle Creek\'s autologous fibroblast candidate process, FCX-007, used to treat patients with dystrophic epidermolysis bullosa (DEB) by reprogramming their cells using a lentiviral vector. I oversee In-process, DS/DP release and Stability assays related to Flow Cytometry, Cell & Molecular Biology, Immunoassays and Compendial Microbiology methods in addition to the site\'s Environmental Monitoring Program.
Education
University of the Sciences in Philadelphia
M.S., Cell Biology and Biotechnology
2001 — 2003
University of Delaware
B.S., Medical Techology
1992 — 1997
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