Prakash Parab
About Prakash Parab
Prakash Parab is the Director of Manufacturing Technology at Bristol-Myers Squibb, with a Ph.D. in Biopharmaceutics from the University of Cincinnati. He specializes in Continuous Process Verification, Drug Product Development by QbD, and has extensive experience in scale-up, tech transfer, and validation processes.
Current Role at Bristol-Myers Squibb
Prakash Parab holds the position of Director of Manufacturing Technology at Bristol-Myers Squibb. In this role, he is responsible for overseeing the implementation and optimization of manufacturing processes within the company. His involvement includes adopting and integrating advanced manufacturing technologies to ensure efficient production and maintain high-quality standards.
Educational Background in Biopharmaceutics
Prakash Parab earned his Ph.D. in Biopharmaceutics from the University of Cincinnati. His education spanned from 1981 to 1986, providing him with a strong foundation in the field. He also studied at Bangalore University, further solidifying his knowledge and expertise in pharmaceutical sciences.
Expertise in Manufacturing Technology and Process Optimization
Prakash Parab has extensive expertise in Continuous Process Verification including Statistical Process Control (SPC), Six Sigma, Process Analytical Technology (PAT), Lean Manufacturing, and Informatics. His skills ensure the continuous improvement and efficiency in manufacturing processes, thereby supporting high-quality production standards.
Specialization in Drug Product Development by QbD
Specializing in Drug Product Development by Quality by Design (QbD), Prakash Parab is proficient in developing various drug forms including tablets, capsules, liquids, creams, lotions, and ointments. His skills encompass the entire spectrum of developing drug products that meet rigorous quality standards.
Experience in Scale-Up, Tech Transfer, and Validation
Prakash Parab brings considerable experience in scale-up processes, technology transfer, and validation. His role involves ensuring that manufacturing processes are effectively scaled from laboratory settings to full production, maintaining rigorous validation protocols throughout these transitions.