Gurpreet Singh

Pharmaceuticals professional with 18 years’ experience in the industry in various leadership and management positions. Experience of working with small molecule and large molecules. Responsible for establishing and managing a broad range of complex global alliances with external BioPharma companies and own the entire alliance management process (from identifying potential partners, understanding their needs, to defining joint projects) and will work closely with our team of Product Managers to ensure a smooth project delivery.

Experience working in oncology, neurology (Als, Alzheimer’s, dementia and TBI), rare diseases, nephrology, respiratory tract infections (PMDI and Nasal Sprays), infectious diseases, GI, pain management therapeutic areas. Extensive laboratory experience, successfully manage business development, projects and delivers organizational and project leadership for drug discovery and Generic commercialization and lifecycle projects which include commercial product development activities, clinical trials, preclinical trails, manufacturing, analytical development, commercial process development, process characterization and validation, new formulations, new manufacturing processes, process and technology transfers and new or platform drug delivery devices.

Regulatory submission experience (NDAs, MAAs, BLA, INDs) includes authoring (Modules 2 and 3) as well as building IND/NDA/MAA submission plans from ground up. Extensive laboratory experience, successfully manages a group of Senior Scientist/Scientists, seamlessly plans and manages the daily activities of the analytical department including the testing, calibration, method development & validation and technology transfers.Pharmaceuticals professional with 18 years’ experience in the industry in various leadership and management positions. Experience of working with small molecule and large molecules. Responsible for establishing and managing a broad range of complex global alliances with external BioPharma companies and own the entire alliance management process (from identifying potential partners, understanding their needs, to defining joint projects) and will work closely with our team of Product Managers to ensure a smooth project delivery. Experience working in oncology, neurology (Als, Alzheimer’s, dementia and TBI), rare diseases, nephrology, respiratory tract infections (PMDI and Nasal Sprays), infectious diseases, GI, pain management therapeutic areas. Extensive laboratory experience, successfully manage business development, projects and delivers organizational and project leadership for drug discovery and Generic commercialization and lifecycle projects which include commercial product development activities, clinical trials, preclinical trails, manufacturing, analytical development, commercial process development, process characterization and validation, new formulations, new manufacturing processes, process and technology transfers and new or platform drug delivery devices. Regulatory submission experience (NDAs, MAAs, BLA, INDs) includes authoring (Modules 2 and 3) as well as building IND/NDA/MAA submission plans from ground up. Extensive laboratory experience, successfully manages a group of Senior Scientist/Scientists, seamlessly plans and manages the daily activities of the analytical department including the testing, calibration, method development & validation and technology transfers.