Paul Guarrera
About Paul Guarrera
Paul Guarrera is the Associate Director of QA Operations at Bristol Myers Squibb, with over 27 years of experience in the pharmaceutical industry.
Current Position at Bristol Myers Squibb
Paul Guarrera currently holds the position of Associate Director QA Operations at Bristol Myers Squibb. In this role, he oversees quality assurance operations, ensuring that all pharmaceutical products meet rigorous standards. His responsibilities likely include managing quality control processes, coordinating with various departments, and maintaining compliance with industry regulations.
Previous Roles at Bristol Myers Squibb
Before his current role, Paul Guarrera served as Manager QA Validation/Tech Services from 2018 to 2020 in Syracuse, New York. Prior to that, he was the Biologics External Manufacturing Operations Manager from 2016 to 2018, also in the Syracuse, New York area. In these positions, he focused on validation processes and external manufacturing operations, contributing to the quality and efficiency of biologics production.
Experience at Hanford Pharmaceuticals
Paul Guarrera worked at Hanford Pharmaceuticals, LLC for 13 years, from 1993 to 2006, in the Syracuse, New York area. During his tenure, he held the role of Process Control & Validation Manager. He was responsible for overseeing process control and validation, ensuring that pharmaceutical processes met all necessary standards and regulations.
Educational Background
Paul Guarrera earned his Bachelor of Science degree in Microbiology and Immunology from Syracuse University. His strong background in these fields has provided a solid foundation for his career in the pharmaceutical industry, particularly in roles related to quality assurance and validation processes.
Industry Expertise
With over 27 years of experience in the pharmaceutical industry, Paul Guarrera specializes in quality assurance operations and validation processes. His extensive experience also includes managing biologics external manufacturing operations, making him a well-rounded professional in the field of pharmaceutical quality management.