Sheila G. Magil, PhD

Sheila Magil, PhD is a CMC and quality expert with more than 30 years of experience working closely with both large and small biopharmaceutical companies to bring novel drugs to patients. As a Principal Consultant with BioProcess Technology Consultants, Sheila has helped many companies implement upstream and downstream manufacturing processes, quality control testing and characterization, cGMP compliance, and validation of manufacturing processes and facilities. Sheila was most recently the Managing Director for BDO USA. Sheila has a proven track record of overseeing successful internal and external development activities and preparing a wide range of regulatory filings to the FDA and EMA including 510Ks, INDs, BLAs for biologics and cell and gene therapy related materials. Sheila received her BA in Chemistry from Carnegie Mellon University and a PhD in Biochemistry from the University of Minnesota.

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