Director of Regulatory Process, Standards and Training, Takeda
Sandeep brings 25+ years of experience in Compliance and Quality Management within the Biotechnology and Pharmaceutical Industry. Has managed teams in R&D, Technical Operations, and IT. He has proven expertise in management of GxP Training Quality Systems, management of regulated Processes & Standards, Computer Systems Validation, 21 CFR Part 11 compliance, IT Quality, IT Application Management, and Corporate (Internal) and External Auditing.