The Regulatory Affairs Executive provides regulatory consulting services to multiple medical device and IVD clients ensuring compliance with ISO 13485:2016 and CDSCO Medical Device Rules MDR 2017 including Import and Manufacturing License support. · ...

The Regulatory Affairs Specialist is responsible for supports the On-Market Sustainment Team by preparing global change notifications and updating technical documentation to maintain product approvals.This role is responsible for compiling and supporting regulatory submission pac ...

The Staff Regulatory Affairs is part of the Miami Regulatory Affairs team and will support new product development global registrations advertising and promotional materials product labeling post market regulatory compliance adapting to new changing regulatory requirements. · ...