Global Regulatory Affairs Specialist – Medical Devices
Listed on 2026-10-06
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Healthcare
Healthcare Compliance, Medical Science Liaison
Ormco is seeking a Regulatory Affairs Specialist to drive global product registrations, maintain regulatory filings, and align with EU MDR requirements. You will collaborate with cross-functional teams and coordinate with global registration partners to support a broad product portfolio.
The role requires 2+ years in regulatory affairs for medical devices or regulated industries, with strong CER/SSCP/PSUR experience, and an on-site work arrangement of at least four days per week.
This role, Global Regulatory Affairs Specialist – Medical Devices at Ormco, could be your next move.
This position is for the Global Regulatory Affairs Specialist – Medical Devices role at Ormco.
We are seeking a motivated Global Regulatory Affairs Specialist – Medical Devices to join Ormco in Brea, CA, United States.
Consider building your career as a Global Regulatory Affairs Specialist – Medical Devices at Ormco.
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