Remote Regulatory Affairs Specialist for Med Dev & IVD

Expedock Software Inc. is seeking an experienced Regulatory Affairs Specialist to work fully remote. You will guide international clients through EU MDR, UKCA, and US FDA frameworks while managing quality systems.

The ideal candidate has at least 2 years in QA/RA within the medical device or IVD sectors and is adept at drafting regulatory submissions. Strong written English skills and independence are essential for this role.