Paul Davila
About Paul Davila
Paul Davila is a Senior Quality Assurance Specialist at Bristol Myers Squibb in Summit, New Jersey, with a strong background in quality assurance within the pharmaceuticals industry.
Current Role at Bristol Myers Squibb
Paul Davila is currently employed as a Senior Quality Assurance Specialist at Bristol Myers Squibb in Summit, New Jersey. In this role, he participates in cross-functional teams aimed at improving quality processes. His work focuses on ensuring compliance with FDA regulations, utilizing his extensive expertise in quality assurance within the pharmaceuticals industry.
Past Experience at Minaris Regenerative Medicine
Paul Davila previously worked as a Quality Assurance Associate at Minaris Regenerative Medicine, formerly known as Hitachi Chemical Advanced Therapeutic Solutions. He served in this role from 2020 to 2021 in Allendale, New Jersey. During his tenure, he contributed to the development of quality assurance protocols, leveraging his background in biomedical engineering to enhance the company's quality standards.
Employment at BioReference Laboratories
From 2018 to 2019, Paul Davila was employed at BioReference Laboratories in Elmwood Park, New Jersey, as a Specimen Processor. This role helped him build foundational skills that he later applied in his quality assurance career within the pharmaceuticals industry.
Educational Background in Biomedical Engineering
Paul Davila holds both a Bachelor's and Master's degree in Biomedical Engineering from the New Jersey Institute of Technology. He completed his Bachelor's degree from 2012 to 2017 and his Master's degree from 2017 to 2021. His academic background provides him with a robust understanding of biomedical engineering principles, which he applies in his work as a quality assurance specialist.
Expertise in Quality Assurance and FDA Compliance
Paul Davila has extensive expertise in quality assurance within the pharmaceuticals industry. He has worked on numerous projects aimed at ensuring compliance with FDA regulations. His roles have often involved participating in cross-functional teams to improve quality processes and develop new quality assurance protocols.