Myant Health is seeking an experienced Regulatory Affairs Manager to lead regulatory strategy and submissions for our medical device and SaMD portfolio in Canada, the United States and Europe. You will collaborate with Product, Engineering, Clinical, Quality and Manufacturing to align development with regulatory requirements. The role requires hands-on experience with Health Canada, FDA and EU MDR pathways, including submissions (510(k)/De Novo, CE marking) and post-market activities, and deep
#J-18808-Ljbffr
📌 Regulatory Affairs Lead for Med Devices & SaMD (Mississauga)
🏢 Myant
📍 Mississauga
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.