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Medical Device & Regulations Engineer

Medical Device & Regulations Engineer

Katalyst HealthCares & Life SciencesSanta Clara, CA, United States
1 day ago
Job type
  • Full-time
Job description

Software Quality Assurance Specialist

Responsibilities : Develop, implement, and maintain software quality assurance processes for non-product software used in medical device development. Ensure adherence to regulatory standards (FDA, ISO 13485, IEC 62304) and industry best practices for non-product software. Support audits and inspections by regulatory bodies, ensuring that non-product software systems comply with quality...

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Engineer Device • Santa Clara, CA, United States

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