Alcon seeks a Manager, Regulatory Operations (Management Path) to drive a controlled documentation system and coordinate global regulatory submission projects. You will guide teams in dossier preparation, submission publishing, licensing, and labeling across medical devices and pharmaceuticals. The role is part of Alcon's Quality & Regulatory Affairs and requires leadership, project management, and regulatory expertise across US, EU, and Canada platforms.

Also on the board Same function, level within a rung

Level

Manager

Location

Lake Forest, CA

Occupation

Regulatory Affairs Managers

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

today

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