Carlos Rodriguez
About Carlos Rodriguez
Carlos Rodriguez is the Associate Director at Bristol Myers Squibb in Puerto Rico, with over 25 years of experience in the pharmaceutical industry.
Current Position at Bristol Myers Squibb
Carlos Rodriguez has been serving as the Associate Director at Bristol Myers Squibb in Puerto Rico since January 2010. In this role, he oversees process investigations, development, validation, and optimization. He is also responsible for product life cycles under the company's robustness program and manages Senior Product Scientists who support business units and commercial manufacturing activities.
Previous Role at Patheon Pharmaceuticals PR
Before joining Bristol Myers Squibb, Carlos Rodriguez worked at Patheon Pharmaceuticals PR as a Six Sigma Black Belt for four months in 2009-2010. During his tenure, he leveraged his Six Sigma certification to improve processes within the organization.
Experience at Legacy Pharmaceuticals Puerto Rico, LLC
Carlos Rodriguez worked at Legacy Pharmaceuticals Puerto Rico, LLC from 2001 to 2009, where he served as Technical Operations Supervisor. In this role, he was involved in various technical operations and managed different aspects of the company's processes.
Early Career at Watson Laboratories Caribe Inc.
Carlos Rodriguez started his career in the pharmaceutical industry at Watson Laboratories Caribe Inc., where he worked as a Technical Services Specialist from 1998 to 2001. During his three-year tenure, he gained significant experience in technical services and process optimization.
Educational Background
Carlos Rodriguez earned a Bachelor's degree in Mechanical Engineering from Universidad Politécnica de Puerto Rico. His engineering education has provided a strong foundation for his extensive career in the pharmaceutical industry.
Pharmaceutical Industry Experience
With over 25 years of experience in the multinational pharmaceutical industry, Carlos Rodriguez is highly skilled in process validations, equipment, facility, and utility qualifications. He is also proficient in the optimization of solid and semi-solid processes and is responsible for the review and approval of regulatory documentation for product optimization and technical transfer.