Luz D. is an experienced professional in quality assurance and regulatory affairs within the medical device sector. Currently serving as the MDR & MDSAP Lead Auditor at SGS since January 2022, Luz D. has previously held significant roles, including CE Marking Auditor at ProductLife Group and Project Manager at Bureau Veritas Group. Expertise includes managing compliance audits, overseeing quality management systems, and consulting on regulatory matters related to medical devices and pharmaceutical products. Luz D. possesses advanced academic qualifications, including a Master's Degree in Quality, Safety, Health, and Environment Management, and a Master of Science in Biochemistry.
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