Amy Aburomi
About Amy Aburomi
Amy Aburomi is the Manager, Supervisor QA Shop Floor Cell Therapy at Bristol Myers Squibb, with over 15 years of experience in the biopharmaceutical industry, specializing in quality assurance and manufacturing roles.
Current Role at Bristol Myers Squibb
Amy Aburomi serves as the Manager and Supervisor for QA Shop Floor Cell Therapy at Bristol Myers Squibb. In this capacity, she is responsible for overseeing quality assurance processes, ensuring compliance with industry standards, and maintaining the integrity of cell therapy manufacturing. Her experience and expertise in QA make her a key asset to the company's operations in this specialized field.
Previous Experience at Gilead Sciences
In 2021, Amy Aburomi worked at Gilead Sciences as a QA Specialist III for a brief tenure of five months in Morris Plains, New Jersey. During this period, she contributed to the quality assurance processes, focusing on compliance and quality control within the organization’s biopharmaceutical operations.
Quality Assurance Specialist at Immunomedics
Amy Aburomi held the position of Senior QA Specialist at Immunomedics from 2019 to 2021. Over the course of two years, she was integral to the QA team, ensuring that the quality standards and regulatory requirements were met. Her role involved supervising QA processes and contributing to the overall quality management system.
Role at Adaptimmune US
Amy Aburomi spent three years at Adaptimmune US from 2016 to 2019 as a Cell Manufacturing Specialist, PIP. CMC Organisation. Her role focused on cell manufacturing processes, contributing to the development and optimization of cell therapy products. Her expertise in cell manufacturing was crucial in advancing the company’s therapeutic programs.
Career at Novartis
Amy Aburomi has held multiple roles at Novartis, including GMP Documentation Coordinator and MFG Supervisor, Process Expert. From 2013 to 2015, she served as MFG Supervisor, ensuring smooth production processes and compliance with manufacturing standards. As GMP Documentation Coordinator from 2015 to 2016, she managed GMP documentation and compliance, vital for the company’s regulatory adherence.
Extensive Industry Experience
With over 15 years in the biopharmaceutical industry, Amy Aburomi has amassed substantial experience in quality assurance and manufacturing roles. She has worked in both large pharmaceutical companies like Novartis and smaller biotech firms such as Adaptimmune and Immunomedics. This diverse experience showcases her adaptability and expertise across different organizational settings.