Accelerating your Business Strategy
World Class Operator
•Proven Leader with 27 years of direct pharma/cell therapy experience
•GMP & Quality expertise across clinical and commercial manufacturing
•Process Development and Supply Chain experience in small, large molecules (DS & DP) •Multiple manufacturing platforms
•Direct CDMO Program/Business Management & Strategy
Technical Expertise
•Expertise using closed and automated manufacturing process platforms
•Expertise using specialized instruments and equipment specific to cell therapy
•Expertise in a variety of cell types CAR T, T cells, NK cells, cancer cell lines, HSCs, iPSCs, MSCs
•Plasmid and mRNA Development and Manufacturing
•Product Development and Launch (CDMO services)
Strategy & Execution
•Full-service CDMO enablement (All modalities)
•Designed, Built and Qualified two (2) Cell therapy facilities (East and West Coasts)
•Strategy Planning
•Competitive Landscape Assessments
•Forecasting (Financial & Capacity)
•Organizational Design
•Workforce Planning and Modeling
Biotech Consulting
Our biotech consulting services provide expert guidance and support to biotech companies and organizations, helping them navigate the complex landscape of biotech innovation.
Background
Dan Garcia Founder & CEO
Mr. Garcia is an executive with operational leadership and expertise (27 yrs) in Cell & Gene Therapy, Large and Small Molecule Development (Process and Analytical), Manufacturing and Testing. Proven financial record of top and bottom-line growth across two cell therapy CDMO start up organizations. Proven outcomes of facility design, build, commissioning, profitability, strategy, talent acquisition and daily operational execution. Prior to starting Cell Therapy Ready, Dan was the General Manager at Thermo Fisher Scientific leading their Cell Therapy CDMO Services Business Unit. Dan worked at Patheon Biologics overseeing strategic business and program management. Prior to his CDMO career Dan spent 17 years at Amgen in various leadership roles within contract manufacturing, operations planning, and clinical and commercial manufacturing. Dan holds an MBA from Pepperdine University and a BS in Biochemistry from the California Polytechnic University.
GMP Facilities - Plasmids, mRNA, Viral Vectors, Cell Therapy, Bio
Design, Build and Qualification of state-of-the-art facilities with working expertise in the operational readiness of all modalities. Experienced leader producing high-quality biologics and cell therapies at scale, helping to bring innovative treatments to market faster.
Productivity Enablement - Forecasting and Workforce Planning
Our bioinformatics expertise and software tools enable us to analyze and interpret complex biological data, providing insights into financial forecast and capacity modeling