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Executive Certificate in Medical Device Quality Assurance
-- ViewingNowMedical Device Quality Assurance: This Executive Certificate equips professionals with essential skills in regulatory compliance, quality systems, and risk management. Designed for quality engineers, regulatory affairs professionals, and medical device professionals seeking career advancement, this program covers ISO 13485, 21 CFR Part 820, and quality system regulations.
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๊ณผ์ ์ธ๋ถ์ฌํญ
- Medical Device Regulations and Standards
- Quality Management Systems (QMS) in Medical Devices
- Risk Management for Medical Devices
- Good Manufacturing Practices (GMP) for Medical Devices
- Quality Auditing and Internal Audits
- CAPA (Corrective and Preventive Actions)
- Design Controls for Medical Devices
- Post-Market Surveillance
- Human Factors Engineering in Medical Device Design
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Career Role Description Medical Device Quality Assurance Specialist (UK) Ensuring compliance with regulatory requirements (e.g., MDR, IVDR) for medical devices throughout their lifecycle.
Expertise in quality management systems (QMS), risk management, and auditing is crucial.
Regulatory Affairs Manager, Medical Devices Navigating the complex regulatory landscape for medical devices in the UK and EU.
Key responsibilities include submissions, approvals, and maintenance of regulatory compliance.
Deep understanding of MDR, IVDR, and other relevant regulations.
Quality Systems Auditor, Medical Devices Conducting internal and external audits to ensure compliance with quality management systems (QMS) standards like ISO 13485.
Experience in medical device manufacturing and quality assurance principles is paramount.
Senior Quality Engineer, Medical Devices Leading quality initiatives, developing and implementing quality control procedures, and driving continuous improvement in medical device manufacturing processes.
Strong problem-solving and leadership skills are essential.
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