Quality Assurance Regulatory Specialist Toronto
MIMOSA Diagnostics
Ensure compliance and product excellence with MIMOSA Diagnostics as a Senior Quality Assurance and Regulatory Affairs Specialist. Work hybrid from Toronto to drive improvements in quality standards.
MIMOSA is committed to compassionate care through innovative solutions and seeks a Senior Quality Assurance/Regulatory Affairs Specialist. This role plays a crucial part in maintaining compliance with regulatory standards governing medical devices. A deep understanding of quality management systems in the medical industry is essential for facilitating audits and collaboration on quality issues.
Key Responsibilities: - Develop quality assurance strategies to meet compliance needs - Perform internal audits and regulatory inspections - Prepare regulatory documentation for Health Canada and FDA - Address regulatory compliance issues with cross-functional teams - Lead product quality investigations and corrective actions
Requirements: - Bachelor’s degree in Science or Engineering - At least 3 years in quality assurance, medical devices preferred - In-depth knowledge of ISO 13485:2016 and regulations - Strong communication and analytical capabilities - Certification in quality assurance is beneficial
Contribute to MIMOSA’s mission of empowering quality healthcare by ensuring compliance and excellence in product offerings.#J-18808-Ljbffr
MIMOSA is committed to compassionate care through innovative solutions and seeks a Senior Quality Assurance/Regulatory Affairs Specialist. This role plays a crucial part in maintaining compliance with regulatory standards governing medical devices. A deep understanding of quality management systems in the medical industry is essential for facilitating audits and collaboration on quality issues.
Key Responsibilities: - Develop quality assurance strategies to meet compliance needs - Perform internal audits and regulatory inspections - Prepare regulatory documentation for Health Canada and FDA - Address regulatory compliance issues with cross-functional teams - Lead product quality investigations and corrective actions
Requirements: - Bachelor’s degree in Science or Engineering - At least 3 years in quality assurance, medical devices preferred - In-depth knowledge of ISO 13485:2016 and regulations - Strong communication and analytical capabilities - Certification in quality assurance is beneficial
Contribute to MIMOSA’s mission of empowering quality healthcare by ensuring compliance and excellence in product offerings.#J-18808-Ljbffr
Vacancy posted 1 hour ago
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