Chris Reynolds is an experienced Program Manager in Commercial Regulatory Affairs at Genentech since February 2022. Previously, Chris served as Senior Manager in Commercial Regulatory Affairs at Dermira, Inc., where Chris established Materials Approval Committees (MAC) to prepare for the company's first commercial product approval and co-led review committees to ensure regulatory compliance across various materials. Earlier roles include Regulatory Affairs Coordinator and Medical Affairs Coordinator at MAP Pharmaceuticals, as well as Senior Associate in Marketing Operations and Regulatory Affairs at Pharmacyclics, an AbbVie Company, where Chris focused on operational efficiencies and was a key point of contact for the Materials Approval & Review Committees (MARC) process.
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