CordenPharma
Lois Hintz is an experienced quality assurance professional with over three decades in the pharmaceutical industry. Currently serving as the QA Manager of Quality Engineering and Validation at Corden Pharma Colorado, Inc. since October 2011, Lois manages a team focused on quality systems and employee development through a risk-based approach. Previously, at Roche Pharmaceuticals from 1996 to October 2011, Lois held the title of Distinguished Process Engineer, leading initiatives for GMP laboratory implementation and overseeing interdisciplinary teams in the production of proof of concept materials. Lois began their career as a Process Engineer at Upjohn from January 1988 to July 1996. Lois earned a Bachelor of Science degree in Chemical Engineering from the University of Wisconsin-Madison between 1981 and 1987.
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CordenPharma
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CordenPharma is your full-service partner in the Contract Development & Manufacturing (CDMO) of APIs, Lipid Excipients, Drug Products and Packaging. Through a network of cGMP facilities across Europe and the US organized under six technology platforms – Peptides, Lipids & Carbohydrates, Oligonucleotides, Injectables, Highly Potent & Oncology, Small Molecules - CordenPharma experts translate complex ideas, processes and projects at any stage of development into high-value pharmaceutical products. Visit to learn more > cordenpharma.com