Head of QA/RA (SaMD)
Winnipeg, MBTélétravailTemps plein
G
GuruLink
10+ ans3+ gestionCandidates need 10+ years in medical device QA/RA, including 5+ years with software as a medical device and 3+ years leading teams. They must have built an ISO 13485 quality system, led FDA submissions to authorization, and know IEC 62304, ISO 14971 and FDA software guidance.
Ketryx, Greenlight Guru, Jira