The Quality Assurance and Regulatory team have an exciting opportunity for a Design Quality Specialist role to support Myant’s drive to medical product commercialization and beyond. The role will focus primarily on assuring quality documentation and processes in the Design, Development and Design Transfer phases of the Product Development life cycle. The ideal candidate will have experience working in Medical Device companies under MDSAP/ISO 13485 QMS and with electronic QMS (eQMS) systems. Alternatively, Health Technology Management (Clinical Engineering) roles and strong familiarity with a range of patient monitoring technologies and applications, along with QMS experience would also be an asset. Myant is in the process of advancing the commercialization of the Skiin garment devices and Software as a Medical Device Products so experience in New Product Introduction (Software in particular) is advantageous. The ideal candidate will demonstrate enthusiasm, results-orientation, and great team play to achieve success in the multidisciplinary roles of this position. The Design Quality Specialist will report into the VP and Quality Assurance and Regulatory Affairs.
Responsibilities:
Qualifications:
What we offer at Myant:
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