Susan Schniepp, distinguished fellow at Regulatory Compliance Associates (RCA), is the knowledge leader responsible for training and advising RCA staff and clients on current trends and issues facing the pharmaceutical, biotechnology and medical device industries. Her background includes cGMPs, audit readiness, change control, investigations, supplier quality and batch record reviews. Ms. Schniepp has more than 40 years’ experience in quality assurance, serving in leadership roles at Allergy Laboratories, OsoBioPharmaceuticals, Searle, Abbott and Hospira. In addition, she served on the Parenteral Drug Association Board of Directors from 2011-2013 and 2016-2019 and currently serves as the Chair.