Jim McGrath is the executive vice president of regulatory affairs and product development for PBM Pharmaceuticals, where he oversees the development and U.S. Food and Drug Administration approval of innovative pharmaceutical and nutritional products.

Before joining PBM, Mr. McGrath held several key management positions in the areas of product development, technical services, quality assurance, and regulatory affairs. He has more than 35 years of experience in the pharmaceutical industry, working for companies such as Wyeth, Rugby-Darby, Circa Pharmaceutical, and NutraMax Products.

Mr. McGrath attended the Wharton executive program at the University of Pennsylvania and is a graduate of New York University, where he earned a BS in chemical engineering.