Regulatory Affairs Lead in Mississauga

Regulatory Affairs Lead in Mississauga

Mississauga Full-Time 90000 - 110000 $ / year (est.) On-site
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At a Glance

  • Tasks: Lead regulatory strategy for innovative wearable medical devices and software.
  • Company: Myant Health, a pioneer in wearable health technology.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Other info: Join a dynamic team dedicated to transforming health through technology.
  • Why this job: Make a difference in healthcare by ensuring compliance and innovation.
  • Qualifications: Experience in regulatory affairs and knowledge of medical device regulations.

The predicted salary is between 90000 - 110000 $ per year.

Myant Health is seeking a Regulatory Affairs Manager to support the commercialization of our SKIIN wearable medical devices and Sa MD.

You will lead regulatory strategy across Canada, the United States and Europe, working with cross-functional teams to translate requirements into actionable development plans.

You will manage regulatory submissions, maintain e QMS documentation, and ensure ongoing compliance with ISO 13485/MDSAP and applicable medical device regulations.

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Regulatory Affairs Lead in Mississauga employer: Myant Inc

At Myant Health, we are at the forefront of healthcare technology, offering a dynamic work environment where innovation thrives. As an R&D Biomedical Engineer, you will be part of a collaborative team dedicated to transforming everyday textiles into intelligent health interfaces, with ample opportunities for professional growth and development. Our commitment to a supportive culture and competitive benefits ensures that you can make a meaningful impact while advancing your career in a rapidly evolving field.

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Contact Details:

Myant Inc Recruitment Team

We think you need these skills to ace Regulatory Affairs Lead in Mississauga

Regulatory Strategy
Cross-Functional Collaboration
Regulatory Submissions
eQMS Documentation Management
ISO 13485
MDSAP Compliance
Medical Device Regulations