Sumitoma Pharma US
Daniel Schuette is an accomplished professional in IT compliance and quality assurance with extensive experience in the pharmaceutical industry. Currently serving as Director of CSV QA IT Engineering at Sumitomo Pharma America, Inc., Daniel directs the computer system validation and IT quality approach for a new eQMS that integrates multiple companies. Previously, Daniel held several key roles, including Sr. Manager of IT Compliance at Sumitomo Pharma Oncology, and Consultant at Hawkins Point Partners, where Daniel focused on maintaining compliance with GxP standards for client systems. Daniel's career also includes significant contributions at Takeda, Cambridge IT Compliance LLC, Genzyme, and Vertex Pharmaceuticals, where responsibilities ranged from QA oversight of system implementations to the development of training programs and protocol documentation. Daniel's academic background includes a Bachelor's degree in Applied Science from Cambridge College and an Associate's degree in Computer Information Systems from DeVry College of Technology.
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