Michael Gomez

Michael Gomez

Associate Scientist Qc Sample Management Car T @ Bristol Myers Squibb

About Michael Gomez

Michael Gomez is an Associate Scientist QC Sample Management CAR-T at Bristol Myers Squibb, with extensive experience in the pharmaceutical industry, including roles at Johnson & Johnson, Novartis, MTF Biologics, LifeCell, and Oticon USA.

Title and Current Role

Michael Gomez is the Associate Scientist QC Sample Management CAR-T at Bristol Myers Squibb. He focuses on quality control and sample management specifically for CAR-T cell therapy. His role involves ensuring the integrity and compliance of samples within the pharmaceutical development process.

Professional Experience at Johnson & Johnson

Michael Gomez worked as a Manufacturing Operation CAR-T at Johnson & Johnson from 2019 to 2022 in New Jersey. During his tenure, he focused on the production and operational aspects pertaining to CAR-T cell therapy. His role included developing operational procedures and ensuring compliance with industry standards.

Employment History at Novartis

From 2018 to 2019, Michael Gomez served as a Production Support Specialist at Novartis in Morris Plains, New Jersey. He contributed to the production support activities and played a pivotal role in maintaining production standards and protocols, enhancing the overall production efficiency.

Career at MTF Biologics, LifeCell, and Oticon USA

Michael Gomez has held various positions in the pharmaceutical and biotechnology sectors. He worked as a Production Operator at MTF Biologics for 7 months in Edison, New Jersey. Prior to this, he was a Production Technician II at LifeCell, An Acelity Company, for 2 years in Branchburg, and a Production Technician at Oticon USA for 2 years in Somerset, New Jersey.

Education and Technical Skills

Michael Gomez studied at Superior Technical Institute, earning High School/Secondary Diplomas and Certificates from 2002 to 2007. He has expertise in statistical quality control, production, and inventory control within the pharmaceutical industry. He is skilled in developing and implementing time standards and is experienced in monitoring manual equipment and maintaining aseptic procedures in production environments.

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