At a Glance
- Tasks: Ensure high-quality production and compliance in medical device manufacturing.
- Company: Join Myant, a leader in innovative medical technology.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Dynamic work environment with a focus on innovation and improvement.
- Why this job: Make a difference in healthcare by improving quality systems and processes.
- Qualifications: Experience in quality engineering and knowledge of ISO 13485/EU MDR required.
The predicted salary is between 72000 - 88000 $ per year.
Myant is seeking a Quality Engineering Specialist to strengthen manufacturing processes, supplier quality and quality systems within a regulated medical device environment. The role focuses on quality assurance, process validation, CAPAs and risk management to ensure compliant, high‑quality production.
Ideal candidates will have a strong quality engineering background in medical devices, experience with ISO 13485/EU MDR, and hands-on capability to drive improvements across Manufacturing.
Medical Device Quality Engineer & Compliance 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.
