Francisco J. Malave Sanabria, Pe
About Francisco J. Malave Sanabria, Pe
Francisco J. Malave Sanabria is the Site Director of OSD Manufacturing and Warehouse Operations at Bristol Myers Squibb, with extensive experience in Oral Solid Dosage manufacturing and project management.
Title
Francisco J. Malave Sanabria serves as the Site Director of OSD Manufacturing and Warehouse Operations at Bristol Myers Squibb.
Current Position at Bristol Myers Squibb
Francisco J. Malave Sanabria is currently employed at Bristol Myers Squibb as the Site Director of OSD Manufacturing and Warehouse Operations. His role involves overseeing the manufacturing and warehouse operations related to Oral Solid Dosage (OSD) forms.
Previous Experience at Bristol Myers Squibb
Francisco J. Malave Sanabria has held multiple positions at Bristol Myers Squibb. From 2019 to 2021, he served as the Site Director for Oral Solid Dosage Operations in Humacao, Puerto Rico. Prior to that, he was the Associate Director of OSD Manufacturing Operations (2018–2019) and OSD Manufacturing Operations Manager (2017–2018). He also worked as the Maintenance and Engineering Manager (2015–2017) and Principal Project Engineer (2013–2015). Francisco began his tenure at Bristol Myers Squibb in 2012 as a Project Engineer.
Past Role at Johnson Controls
Before rejoining Bristol Myers Squibb, Francisco J. Malave Sanabria worked at Johnson Controls as a Project Manager from 2011 to 2012. In this role, he managed various engineering projects, further enhancing his project management skills.
Education and Mechanical Engineering Background
Francisco J. Malave Sanabria earned a Bachelor of Science degree in Mechanical Engineering from the Universidad de Puerto Rico, where he studied from 1995 to 2001. His engineering background serves as the foundation for his extensive career in project management and OSD manufacturing operations.
Expertise in Oral Solid Dosage Manufacturing
With years of experience in OSD manufacturing operations, Francisco J. Malave Sanabria has a deep understanding of managing and overseeing these processes. His roles at Bristol Myers Squibb have provided him with substantial expertise in this area, ensuring high standards of production and compliance.
Skills in Good Manufacturing Practices (GMP) and Quality Systems
Francisco J. Malave Sanabria has demonstrated a strong background in implementing and maintaining Good Manufacturing Practices (GMP) in the pharmaceutical industry. His responsibilities have included ensuring compliance with industry standards and managing quality systems effectively.
Proficient in Change Control Management
Throughout his career, Francisco J. Malave Sanabria has managed change control processes within the pharmaceutical sector. His ability to oversee and implement changes successfully has been a key aspect of his roles at Bristol Myers Squibb.