Sr. RA Associate Consultant
Remote
Core
Sr. Regulatory Affairs Consultant creating and updating Technical Documents (TDs) for medical device clients in compliance with EU MDR and global regulations.
Role type
Senior Regulatory Affairs Consultant (Contract)
Builds
Technical Documents (TDs) for medical device regulatory submissions
Domain
Medical Devices / Regulatory Affairs
Required skills
EU MDR knowledge, ISO13485 knowledge, FDA Medical Device regulations knowledge, Technical Document drafting, Quality Control checks, PLM system usage, Adobe PDF management, Cross-functional collaboration, Project status reporting
Preferred skills
Life sciences degree, Self-starter attitude, Strong organizational skills (via careerplan.io/jobs/4999261101-sr-ra-associate-consultant-at-clinchoice)
Technologies
Microsoft Office (Word, Excel, PowerPoint), PLM, Adobe PDF