Regulatory Affairs Specialist - FDA/CDER, Combo Products
Becton , Dickinson and Company
Becton Dickinson is seeking an experienced Regulatory Affairs professional in the United States to manage regulatory activities for combination devices and pharmaceuticals, including domestic submissions such as NDA/ANDA and labeling approvals. The role involves coordinating with Marketing, R&D, Manufacturing, and Quality to ensure timely submissions and adherence to FDA guidance, with a focus on CDER regulatory requirements and quality systems. #J-18808-Ljbffr Becton , Dickinson and Company
Vacancy posted 1 day ago
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