Manuel Segarra
About Manuel Segarra
Manuel Segarra is a Manager Sr QA Scientist at Bristol Myers Squibb in Manati, Puerto Rico, with over 10 years of experience in Quality Control, Manufacturing, and Technical Services within the pharmaceutical industry.
Current Role at Bristol Myers Squibb
Manuel Segarra is currently employed at Bristol Myers Squibb as a Manager Sr QA Scientist. He assumed this role in July 2021 and is based in Manati, Puerto Rico. His responsibilities include overseeing quality assurance processes and ensuring compliance with industry standards.
Previous Experience at The Janssen Pharmaceutical Companies
Before joining Bristol Myers Squibb, Manuel Segarra worked at The Janssen Pharmaceutical Companies of Johnson & Johnson. He served as a Senior Operation Support Specialist from 2020 to 2021 in Gurabo, Puerto Rico. Prior to that, he was a Technical Operation Scientist from 2019 to 2020, contributing to various operational and technical projects.
Career at Johnson & Johnson
Manuel Segarra had an extensive tenure at Johnson & Johnson, where he held multiple roles. From 2018 to 2020, he served as a Technical Operation Scientist in Manati, Puerto Rico. Earlier, he was a Senior Manufacturing Process Team Leader from 2014 to 2018, and a Quality Control Specialist from 2013 to 2014. His roles focused on enhancing manufacturing processes and maintaining quality control standards.
Educational Background
Manuel Segarra's educational qualifications include a Bachelor's degree in Chemistry from the University of Puerto Rico-Mayaguez. He also studied Biotechnology at the same institution, achieving a Training in Biotechnology Manufacturing in 2012. Additionally, he completed internships in Bioengineering and Biomedical Engineering at the University of Pittsburgh, and in Chemistry at the University of Massachusetts, Amherst.
Certifications and Expertise
Manuel Segarra holds a Green Belt certification in Lean Six Sigma, reflecting his expertise in process improvement methodologies. With over 10 years of experience in Quality Control, Manufacturing, and Technical Services within the pharmaceutical industry, he has a strong track record of enhancing operational efficiencies and ensuring quality standards in manufacturing processes.