Advanced Medicine Partners
Daniel Udo Onuoha is a highly skilled Senior Process Engineer at Advanced Medicine Partners, with a rich background in bioengineering and pharmaceutical sciences. Prior to this role, Daniel worked at Tune Therapeutics as an Associate Engineer/Scientist and Sr. Research Associate/Engineer in the Vector Core. Daniel's experience includes positions at Novartis Gene Therapies, where responsibilities varied from Interim Supervisor to Bioprocess Engineer II, and at AveXis, Inc. as a BioProcess Engineer I. Daniel's earlier roles include serving as a Laboratory Research Assistant at BRITE, North Carolina Central University, focusing on innovative cancer research, and as a QC Chemist Intern at Novo Nordisk, emphasizing quality control in pharmaceutical testing. Education includes a Master’s degree in Microbial Biotechnology from North Carolina State University, a Bachelor's degree in Pharmaceutical Sciences from North Carolina Central University, and an Associate of Science degree in Pre-Pharmacy Studies from Durham Technical Community College.
Advanced Medicine Partners
Advanced Medicine Partners’ aims to set a new standard for manufacturing and testing innovative medicines that can potentially transform the lives of patients and families. The company delivers process development, manufacturing, analytical development and testing for advanced therapy products, including gene therapies. The company has the experience and capabilities to work with multiple platforms and modalities, including adeno-associated virus (AAV), lentivirus and other delivery systems. Advanced Medicine Partners leverages one of the most experienced genetic medicines teams – at all levels, from bench to boardroom – in the industry, and its exclusive manufacturing platform consistently produces yields that are among the highest in the industry and purity profiles that push the boundaries of what’s possible. The company’s proprietary adeno-associated virus (AAV) manufacturing process minimizes process and product-related impurities and consistently generates industry-leading functional full capsid ratios and best-in-class yields. This manufacturing process prioritizes patient safety while reducing cost of goods and will strive to set the standard for what regulatory agencies expect and patients deserve. Advanced Medicine Partners brings extensive operational experience from Jaguar Gene Therapy and other biotechnology companies. The Advanced Medicine Partners team has manufactured upwards of 350 total non-GMP batches and supplied over 20 preclinical studies, including initial new drug application (IND) enabling efficacy and good laboratory practice (GLP) toxicology studies. The company distinguishes itself from CDMOs by its partnership philosophy. Traditionally, CDMO operations work independently of their clients. Advanced Medicine Partners changes that dynamic by acting as a client’s extended workbench, removing CMC activities from the critical path, and offering real-time data to help clients drive decisions and accelerate their programs.