Daiichi Sankyo
Chirag Patel, MS-PhEn, ASQ-CQA, is an experienced quality assurance professional currently serving as Associate Director of QA GMP Audits at Daiichi Sankyo, Inc. since June 2020, with a prior role as Audit Manager in the same department. Previous positions include Sr. Compliance Officer at Cambrex, Sr. Quality/Compliance Supervisor at Leading Pharma, Quality Compliance Auditor/Specialist at G&W Laboratories, QA Specialist at West-Ward Pharmaceuticals, and IPQA Specialist at US Pharma Lab. Chirag holds a Master’s Degree in Pharmaceutical Engineering from the New Jersey Institute of Technology and a Bachelor’s Degree in Pharmaceutical Sciences from Gujarat University. Additionally, certifications in Supplier Audits and as a Certified Quality Auditor (ASQ-CQA) have been obtained, enhancing expertise in quality assurance and compliance.
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Daiichi Sankyo
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Daiichi Sankyo Co., Ltd. engages in the research, development, manufacture, and sale of pharmaceutical products. It operates through the following segments: Daiichi Sankyo Group and Ranbaxy Group. The Daiichi Sankyo Group segment comprises of Daiichi Sankyo Co., Ltd. and its subsidiaries. The Ranbaxy Group segment includes its core company, Ranbaxy Laboratories Ltd. Both group segments deal with business activities in prescription drugs and general pharmaceutical products. The company was founded on September 28, 2005 and is headquartered in Tokyo, Japan.