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Principal Regulatory Affairs Specialist

Pulmonx • Redwood City, CA, US • published 2026-10-13 08:22:57.520568

Description

**Redwood City, CA** **Hybrid** *The standard work arrangement for this role is hybrid, with an expectation of working onsite at Pulmonx’s Redwood City, California facility at least three days per week. Pulmonx may consider a U.S.\-based remote arrangement for an exceptionally qualified candidate whose experience closely aligns with the role. Remote candidates should expect periodic travel to Redwood City for team meetings, planning, and other business needs.* **Position Overview** The Principal Regulatory Affairs Specialist drives the full spectrum of regulatory activities, from initial market authorization through post\-market compliance, for Pulmonx's US and international device portfolio. This highly visible role shapes FDA and international regulatory strategy, owns change management processes, and serves as a trusted regulatory resource for cross\-functional teams and senior leadership. A primary aspect of the role is ownership of Regulatory Affairs activities for global adverse\-event reportability assessments and timely submission and follow\-up of required regulatory reports, in routine partnership with the QA Complaint Management team. **Key Responsibilities** * Define an...

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