Ting Lin Toledo, Pharm D, R Ph

Ting Lin Toledo, Pharm D, R Ph

Associate Director, Regulatory Affairs Labeling @ BeiGene

About Ting Lin Toledo, Pharm D, R Ph

Ting Lin Toledo, PharmD, RPh, is the Associate Director of Regulatory Affairs Labeling at BeiGene in Los Angeles, California. She has over a decade of experience in regulatory affairs, having held senior roles at Amgen and Sanofi, and has also worked as an Adjunct Assistant Professor at MCPHS University.

Company

Ting Lin Toledo is currently working at BeiGene as an Associate Director, Regulatory Affairs Labeling. Based in Los Angeles, California, BeiGene is a global biotechnology company. The role involves strategic oversight and management of regulatory labeling requirements for the company's pharmaceutical products.

Title

Ting Lin Toledo holds the position of Associate Director, Regulatory Affairs Labeling at BeiGene. She is responsible for ensuring compliance with regulatory labeling standards, managing labeling projects, and working closely with cross-functional teams to support product approvals and post-marketing activities.

Education and Expertise

Ting Lin Toledo earned a Doctor of Pharmacy (PharmD) degree from Northeastern University, where she studied pharmacy from 2009 to 2014. She also obtained a Graduate Certificate in Regulatory Affairs from Massachusetts College of Pharmacy and Health Sciences in 2015. Her expertise encompasses both academic and industry settings, with a strong emphasis on global regulatory affairs and labeling strategy.

Background

Ting Lin Toledo began her career in the pharmaceutical industry as a Regulatory Affairs Postdoctoral Fellow at Sanofi, gaining specialized experience early on. She later transitioned to roles such as Manager, Global Labeling Strategist at Sanofi, and Senior Manager, Global Labeling Strategist at Amgen. Her background includes a solid foundation in both regulatory affairs and academic teaching, having served as an Adjunct Assistant Professor at MCPHS University.

Achievements

Ting Lin Toledo has accrued over a decade of experience in regulatory affairs. Her career includes pivotal roles at Sanofi and Amgen, where she honed her skills in global labeling strategy. Noteworthy is her seamless transition from academia to the pharmaceutical industry, leveraging her regulatory expertise to achieve significant career advancements.

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