Hands on bioprocess expertise, delivered by principals.

Luis joined the firm in 2020 and brings over two decades of biotechnology and biopharmaceutical experience. His technical depth covers upstream and downstream processing, with particular focus on monoclonal antibody cell culture and purification. Luis is grounded in the principle that quality extends beyond technical rationale into the safety and care owed to the patients and communities biologics serve. He holds a Master of Science from West Chester University of Pennsylvania.

JaLisa joined the firm in 2020 and leads operations and quality management. Her work centers on practical application of quality tools, including FMEA, DMAIC, and root cause analysis for non conformance prevention in cGMP environments. Earlier in her career she served in the United States Air Force and held operational roles in healthcare at the U.S. Department of Veterans Affairs and Tampa General Hospital. She holds a Bachelor of Science from the University of Missouri Columbia and a Master of Science from Arizona State University.

Emma brings manufacturing science and technology expertise to upstream cell culture and bioreactor engineering engagements. Her published work spans bioreactor characterization at commercial scale, oxygen mass transfer modeling, CO2 control strategies for large molecule manufacturing, and the lactate metabolic shift in mammalian cell lines. She has also co authored peer reviewed studies on validation methodology for microbial control and process hold times. Emma's engineering grounding helps clients translate development scale processes into robust large scale manufacturing.