Rocco Buffolino
About Rocco Buffolino
Rocco Buffolino is the Principal Process Development Engineer for Device and Packaging Technology at Bristol-Myers Squibb in New York, with over a decade of experience at the company and a background in engineering roles at BD and Johnson & Johnson.
Current Position at Bristol-Myers Squibb
Rocco Buffolino currently serves as the Principal Process Development Engineer in Device and Packaging Technology at Bristol-Myers Squibb. Located in New York, New York, he has been with the company since February 2013. In his role, he specializes in process development within the pharmaceutical industry, focusing on device and packaging technology. His responsibilities likely include designing and improving processes related to medical device manufacturing and packaging solutions for pharmaceutical products.
Previous Experience at BD
Before joining Bristol-Myers Squibb, Rocco Buffolino worked as a Project Engineer at BD (Becton, Dickinson and Company) from 2007 to 2013. During his six years in Franklin Lakes, New Jersey, he was involved in various engineering projects that contributed to the company's medical device sector. His role would have encompassed developing and managing project timelines, ensuring compliance with regulatory standards, and improving processes related to medical devices.
Engineering Role at Johnson & Johnson
Rocco Buffolino's extensive experience includes an eleven-year tenure at Johnson & Johnson as a Staff Engineer. From 1996 to 2007, he worked in Skillman, New Jersey, where he focused on engineering aspects within the medical device industry. At Johnson & Johnson, his responsibilities would have included process development, quality assurance, and project management, all aimed at enhancing the performance and reliability of medical devices.
Specialization in Device and Packaging Technology
Rocco Buffolino is specialized in device and packaging technology within the pharmaceutical industry. His expertise lies in the development and optimization of processes related to the manufacturing and packaging of medical devices and pharmaceutical products. This specialization involves ensuring that devices meet industry standards and regulations while also being efficient and cost-effective in their production and packaging.