Hybrid Global Regulatory Affairs Specialist, Medical Devices
Listed on 2026-10-07
-
Healthcare
Healthcare Compliance, Medical Device Industry, Medical Science Liaison
Theragenics, the parent company behind Arrotek, seeks a Regulatory Affairs Specialist to drive global regulatory compliance and submissions for medical devices across domestic and international markets.
You will collaborate with Quality, Engineering, Operations, and Documentation teams to manage FDA 21 CFR 820, ISO 13485, EU MDR, and regulatory filings, ensuring timely approvals and ongoing compliance in a hybrid role.
We are seeking a motivated Hybrid Global Regulatory Affairs Specialist, Medical Devices to join Arrotek Medical Ltd in Garland, TX, United States.
We have an opening for a Hybrid Global Regulatory Affairs Specialist, Medical Devices in Garland, TX, United States within Legal, Management & Operations.
This role, Hybrid Global Regulatory Affairs Specialist, Medical Devices at Arrotek Medical Ltd, could be your next opportunity.
Are you ready to take on the Hybrid Global Regulatory Affairs Specialist, Medical Devices role at Arrotek Medical Ltd?
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).