Validant
Joseph Schmitt is an experienced pharmaceutical and consulting professional with a robust background spanning several prestigious companies. Currently serving as a Consultant at Treximo since September 2017 and as Owner of JLPS Pharmaceutical Consulting, LLC since April 2017, Joseph also holds the role of QC Manager at Aprecia Pharmaceuticals and works as a Pharmaceutical/Medical Device Consultant at Kinsale Holdings. Previously, Joseph served as a Research Scientist II at Celgene Corp, where responsibilities included overseeing method transfers and revising SOPs, and as Manager/Team Leader at Pfizer, focusing on analytical development and troubleshooting. Joseph's early career included a position as Senior Research Scientist at Bristol-Myers Squibb, managing a team of analytical chemists throughout drug development phases. Joseph holds a Bachelor's Degree in Chemistry from Ramapo College of New Jersey and a Master's Degree in Chemistry from Rutgers University, along with 15 postgraduate credits.
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Validant
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Validant is a full-service life science consulting firm serving developers and manufacturers of pharmaceuticals, biologics, medical devices, and diagnostics worldwide. We partner with these companies to ensure safe and reliable access to life-saving healthcare products, facilitating their efficient, compliant progression from preclinical and clinical phases through to manufacturing and distribution—and optimizing quality at each step. Our platform brings together leading specialists in each facet of the product lifecycle, and we have curated an extensive and diverse global network of consultants to help execute strategies worldwide. Because of this, Validant is able to deliver our breadth of consulting, execution, and support services in the right place, at the right level, and in the right combination to meet your exact need. We've empowered hundreds of clients – from start-ups to the largest global leaders – to efficiently navigate regulatory, compliance, and quality complexities. How can we help you?