Gashbin Hossain currently serves as the Head of QA/RA Medical Device and a member of the Executive Committee at GPI France, focusing on quality and regulatory standards for Medical Device Software in compliance with IEC 62304 and EU MDR. Gashbin possesses extensive experience in developing and maintaining ISO 13485 and ISO 9001 Quality Management Systems, as well as insights in quality assurance and regulatory affairs for Medical Device Software across various classes at Labu Services. Previous roles include Business Development Representative QA/RA at Earlab Co., where Gashbin contributed to medical device prototype development, and supply chain management at Khanem International BV, focusing on market analysis and product line oversight. Early career experiences included quality assurance roles in pharmaceutical settings, emphasizing GMP standards and medication safety, complemented by a solid educational background in Pharmaceutical Business Administration and ongoing studies in eHealth and Self-Management at the University of Amsterdam.
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