McKesson seeks a Lead Counsel to provide strategic legal advice on matters related to Food & Drug Administration (FDA) Quality Management Systems and regulations. Reporting to the VP, Assistant General Counsel, the Lead Counsel will work closely with the legal, compliance, and operational teams supporting our North American business units on the full portfolio of McKesson’s FDA-regulated offerings. As an expert in his/her field, the Lead Counsel will be particularly engaged on issues relating to McKesson’s business and that of its customers and suppliers, including, pharmaceutical private label products, 3PL, REMS programs, clinical research programs, pharmaceutical and medical device distribution, Quality Management Systems and compliance, marketing authorizations, post-market surveillance advertising and promotion, management of manufacturer recalls as well as interaction with regulatory bodies and customers.