Chika Wasyl

Chika Wasyl

Labeling Lead @ Bristol Myers Squibb

About Chika Wasyl

Chika Wasyl is the Director of Global Labeling at Pfizer and also serves as a Labeling Lead at Bristol-Myers Squibb in Wallingford, CT.

Title

Chika Wasyl holds the title of Labeling Lead and currently serves as Director, Global Labeling at Pfizer. Additionally, Wasyl works at Bristol-Myers Squibb in Wallingford, CT, fulfilling the role of Labeling Lead.

Current Roles at Pfizer and Bristol-Myers Squibb

Chika Wasyl has been contributing to Pfizer since January 2018, where she leads the global labeling efforts as Director, Global Labeling. Parallelly, she upholds the position of Labeling Lead at Bristol-Myers Squibb in Wallingford, CT. This dual role underscores Wasyl's extensive expertise and commitment to excellence in the field of pharmaceutical labeling and regulatory affairs.

Work History at Bristol-Myers Squibb

Chika Wasyl's tenure at Bristol-Myers Squibb spans over 15 years. Initially, she worked as a Contract Medical Writer and Japanese Translator from 1990 to 2002. Later, she served as Associate Director, Medical Communications from 2002 to 2005. Her consistent service across various roles at Bristol-Myers Squibb demonstrates her profound knowledge and expertise within the pharmaceutical industry.

Expertise in Japanese Translation and Medical Writing

Chika Wasyl is notable for her expertise in Japanese translation, a rare skill in the global labeling and regulatory affairs domain. Additionally, she specializes in labeling strategy and medical writing, highlighting her proficiency in creating and managing product labels that comply with regulatory standards. This unique combination of skills equips her to handle complex regulatory challenges effectively.

Experience in Global Labeling and Regulatory Affairs

Having worked with Pfizer for over five years as Director, Global Labeling, and amassed 15 years of experience at Bristol-Myers Squibb, Chika Wasyl brings deep expertise in global labeling and regulatory affairs. Her roles have consistently involved strategizing and overseeing the creation of compliant product labels, reinforcing her capability in this specialized field.

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