Technical Director Stallion Laboratories Private Limited, Ahmedabad, India Overall Head for Quality, Strategic planning, Quality compliance, Risk management, Process improvement in Manufacturing, Analytical, Packaging, Validation and Regulatory auditing for Rx, Generics with expertise in every facet of GMP and GXP platform. To lead R&D (Formulation & Analytical), IP, Clinical/BE, ANDA’s and EU Generics (OSD). New formulation site commissioned in 2020, then filed 02 ANDA and this site got USFDA approved in June 2023. Overall responsibility R&D, act as the Stage Gate for products at the engineering batch and submission stage of new Product introductions, handling of CMO / CDMO Projects.