Lifei (Annie) Wang

Lifei (Annie) Wang

Associate Director, Regulatory Affairs Operations @ BeiGene

About Lifei (Annie) Wang

Lifei (Annie) Wang is the Associate Director of Regulatory Affairs Operations at BeiGene, with over 12 years of experience in regulatory submissions publishing and management within the pharmaceutical industry.

Current Role at BeiGene

Lifei (Annie) Wang serves as the Associate Director, Regulatory Affairs Operations at BeiGene. In this role, she is responsible for overseeing regulatory affairs operations and ensuring the accuracy and compliance of regulatory documentation. Her work heavily emphasizes regulatory policy, strategy, and operational efficiencies. Wang's expertise in eCTD publishing and management supports BeiGene's regulatory submissions and interactions with health authorities.

Previous Experience at BeiGene

Before her current role, Lifei Wang worked as Senior Manager II, Regulatory Affairs Operations, at BeiGene from 2019 to 2021. During this period of 2 years, she played a critical role in managing regulatory submissions and documentation. Her experience at BeiGene has been marked by a dedication to maintaining high standards of accuracy and customer service in regulatory affairs.

Professional Background at Pfizer

Lifei Wang has an extensive background at Pfizer, holding multiple positions from 2009 to 2019. She started as a Submission Publishing Specialist and Tech Supervisor in Shanghai, China, and progressively advanced to Hub Submission Manager and Team Manager for APAC Submissions Management. Her tenure at Pfizer spanned 10 years, during which she gained significant experience in regulatory submissions management and publishing, specifically within the APAC region. Her final position at Pfizer was as a Senior Team Manager for APAC Submissions Management, where she served for 4 months in 2019.

Education and Academic Background

Lifei Wang holds both a Bachelor's Degree in Pharmacy and a Master's Degree in Public Health from Fudan University. Her academic background has provided her with a solid foundation for her career in regulatory affairs within the pharmaceutical industry. Her education in pharmacy and public health underpins her deep understanding of regulatory requirements and strategies.

Expertise in Regulatory Submissions

With over 12 years of experience in regulatory submissions publishing and management, Lifei Wang is proficient in handling complex regulatory documentation and eCTD publishing. Her career has consistently focused on regulatory policy, strategy, and operations. Wang places a strong emphasis on the accuracy of regulatory documentation and exceptional customer service, ensuring compliance and efficiency in all her regulatory affairs activities.

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