Henning Moeller is a Director of Quality Engineering GLO with a broad range of experience in the medical device industry, focusing on ISO 13485 and 21 CFR Part 820 compliance. Previously, Henning served as a Senior Program Manager at Stryker and a Program Manager during the M&A process at Stryker Leibinger GmbH & Co. KG, where they coordinated supplier quality teams and managed supplier audits and development. Henning is currently pursuing a Dr. Ing. degree in Maschinenbau at RWTH Aachen University.
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