Quan Young

Quan Young

Quality And Compliance In Market Cluster Lead @ Bristol Myers Squibb

About Quan Young

Quan Young is the Quality and Compliance In-market Cluster Lead at Bristol-Myers Squibb in New Jersey, with extensive experience in quality assurance and compliance across multiple regions.

Current Role at Bristol-myers Squibb

Quan Young currently serves as the Quality and Compliance In-Market Cluster Lead at Bristol-myers Squibb. Based in New Jersey, United States, Quan's role involves overseeing quality assurance and compliance activities within market clusters. His extensive background in these areas supports his current responsibilities, ensuring that products meet regulatory standards and that quality processes are optimized.

Professional Experience at Takeda Pharmaceuticals

From 2013 to 2018, Quan Young worked at Takeda Pharmaceuticals in Tokyo, Japan. During these five years, he held the positions of Manager Quality Assurance GDP and Responsible Person, as well as Deputy Responsible Person. His role primarily involved managing and overseeing the quality assurance processes, ensuring compliance with global standards and regulatory requirements.

Previous Roles at Johnson & Johnson

Quan Young served at Johnson & Johnson from 2010 to 2013 in New Brunswick, New Jersey, United States. He was the Regional Quality Manager and Senior a Trans and TMP Q and C. In these roles, he was responsible for regional quality management, emphasizing the implementation and maintenance of quality standards across various product lines.

Educational Background and Languages

Quan Young holds an MBA in Management & Business Administration from Aalto University, completed between 2001 and 2004. He also earned a Bachelor's degree in Material Science & Engineering from the University of Florida, from 1989 to 1996. Additionally, he studied German at Colón Sprachschule in Hamburg, obtaining the Deutsch (B2) Zertifikat, and is fluent in German.

Career Beginnings and Quality Assurance Expertise

Quan Young began his career as a Quality Trainee at Eimo Oy, before moving on to roles at major global companies. His work at Nokia for nine years, from 1997 to 2006, as a Process and Quality Engineer and Global Concept Owner, established his expertise in quality and process management. He further pursued product lifecycle management at GE Healthcare and held a brief position as Product Quality Manager at Kaz Europe.

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