Senior Global CMC Regulatory Lead; Hybrid

Xeris Pharmaceuticals, Inc. is seeking a Senior Manager of CMC Regulatory Affairs to lead global regulatory development plans and drive successful execution with cross-functional teams.

You will serve as the CMC regulatory lead for assigned products, prepare global CMC content for INDs/NDAs/MAAs/IMPDs, and provide regulatory guidance to Operations and Quality. A BS in a scientific discipline with at least 5 years in pharma, including CMC, is required; hybrid work with some on-site and travel.

Step into the Senior Global CMC Regulatory Lead (Hybrid) role at Xeris Pharmaceuticals Inc in GA, United States and grow with us.

Please review the full job details above before applying.

If your experience matches this role, we encourage you to apply.

All applications are reviewed carefully by our team.