Director of Regulatory Affairs – Indiana


This individual’s primary role is to support regulatory strategy for product development and manufacturing activities to ensure compliance with GMP regulations and to support preparation and filing of regulatory submissions for clients.


Company Profile:

This leading biotech company manufactures both drug substance and product at the facility and focus on mammalian cells. They have experienced double digit growth over the past decade and recently completed an expansion of their award-winning facility. They are located within a short drive of a metropolitan area in the Midwest in a highly desirable city described by the Washington Post as a “Cultural Powerhouse”, known for wine vineyards, 5 star restaurants, museums and art studios, excellent schools, and a University rated as one of the top 5 most beautiful in the country. 

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