Yuri Han
About Yuri Han
Yuri Han is a Quality Assurance Manager at Bristol Myers Squibb in Summit, New Jersey, with extensive experience in quality assurance and compliance roles across various pharmaceutical companies.
Title and Current Position
Yuri Han is a Quality Assurance Manager at Bristol Myers Squibb, based in Summit, New Jersey, United States. In this role, Yuri supervises quality assurance processes and ensures compliance with industry standards.
Previous Roles in Quality Assurance
Yuri Han held several key positions at Akorn, Inc. Before becoming a Quality Assurance Manager at the company for five months from 2020 to 2021, Yuri was a Quality Assurance Supervisor for ten months from 2019 to 2020. Prior to this, Yuri served as a Compliance Supervisor at Sanofi for seven months in 2019 and was a Quality Assurance Specialist there from 2018 to 2019. These roles were primarily focused in Somerset and Ridgefield, New Jersey.
Earlier Career in Biotechnology
From 2016 to 2017, Yuri worked as a Biotech Production Specialist II at Regeneron Pharmaceuticals, Inc. in Rensselaer, New York. Prior to that, Yuri gained significant experience as a Technical Laboratory Specialist at Micra Biotechnologies, Inc. in River Edge, New Jersey, from 2011 to 2015.
Educational Background
Yuri Han holds a Bachelor's degree in Biomedical Engineering and a Certificate in Packaging Engineering from Rutgers University. The Bachelor's degree was obtained through a three-year period from 2013 to 2016, while the Certificate was completed in one year from 2015 to 2016.
Implementing Continuous Improvement Programs
At Bristol Myers Squibb, Yuri Han implemented a continuous improvement program that successfully reduced quality-related incidents by 15%. This highlights Yuri's commitment to enhancing quality assurance processes and fostering a culture of continuous improvement within the organization.
Training and Development
Yuri developed a comprehensive training module for new hires in the Quality Assurance department at Bristol Myers Squibb. This initiative ensured that new team members were well-prepared and knowledgeable about quality processes and standards from the outset.
Leadership in FDA Audit Preparation
Yuri Han led a cross-functional team to achieve inspection readiness for a major FDA audit at Bristol Myers Squibb. This role involved coordinating between departments and ensuring compliance with all regulatory requirements.
Contributions to Industry Knowledge
Yuri has contributed to industry knowledge by publishing an article on aseptic pharmaceutical manufacturing best practices in a leading industry journal. Additionally, Yuri presented on the topic of data integrity in pharmaceutical manufacturing at the International Society for Pharmaceutical Engineering (ISPE) conference.