Accomplished development scientist in advancing small and large molecule sterile drug products for Human and Animal Health markets. Experienced contributor to development teams by providing applied scientific based solutions. Highly experienced in technology transfer, scale-up, experimental design with technical project management and manufacturing experience at R&D facilities and numerous commercial and clinical manufacturing facilities.Significant experience working with CDMO’s in both the USA and Europe.Strong global CMC registration experience supporting drug product approvals including IND's, NDA's, MAA's, BLA and JNDA's, resulting in commercially launched drug products.Proven ability to effectively lead multiple projects simultaneously, working under minimal supervision to meet project milestones on time. As a NYS registered pharmacist, I also bring an end users perspective to the drug products I've developed. As a consultant, my goal has been to utilize this experience base in supporting organizations to effectively deliver drug products to the clinic and the commercial market including CMC registration. I provide development appropriate services to organizations seeking guidance and leadership in technical project management, scale-up, experimental design and execution as well as process development focusing on sterile drug products.Specialties: Effective late stage product development technical leadership of parenteral (lyophile and solutions) and oral liquid dosage forms. Scale-up, technology transfer and CMC registration authorship and strategy of parenteral and oral liquid drug products. Interfacing with CMO's on late stage drug products. I also have broad and varied experience in process development and manufacturing troubleshooting.