Teams at OXOS Medical

Ensure manufacturing processes comply with FDA 21 CFR 820 and ISO 13485. Lead process and test method validations, review and release DHRs, manage nonconformances and CAPAs, maintain quality documentation, conduct line audits, support supplier quality, and drive continuous improvement and risk management for a cleared portable x-ray device.

The Regulatory Specialist will manage regulatory requirements, submit documents, ensure compliance, and collaborate with teams on regulatory strategies and changes.

The Growth Marketing Manager will drive demand generation, oversee analytics and performance marketing, manage vendors, and implement AI workflows to enhance marketing effectiveness.