Regulatory Affairs Specialist - FDA/CDER, Combo Products
Listed on 2026-10-16
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Quality Assurance - QA/QC
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Healthcare
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.
We have an opening for a Regulatory Affairs Specialist - FDA/CDER, Combo Products in Vernon Hills, IL, United States within Legal, Management & Operations.
We would love to welcome a new Regulatory Affairs Specialist - FDA/CDER, Combo Products to our group in Vernon Hills, IL, United States.
For the Regulatory Affairs Specialist - FDA/CDER, Combo Products position at BD, we are reviewing applications now.
Step into the Regulatory Affairs Specialist - FDA/CDER, Combo Products role at BD in Vernon Hills, IL, United States and grow with us.
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