Eti Mermelstein is a skilled professional with extensive experience in regulatory affairs and quality assurance within the medical and pharmaceutical sectors. Serving as the Quality Assurance Regulatory Affairs Manager at Tzamal Medical Group since September 2021, Mermelstein previously held the position of Senior Regulatory Affairs Medical Device Specialist at Raz Pharmaceutics and worked as a Senior Clinical Trial Coordinator at ClinTec International. Earlier experience includes serving as a Senior Clinical Trial Associate at Quintiles from 2006 to 2014, where participation in various clinical studies from inception to closure was a key focus. Mermelstein holds a Master’s Degree and a Bachelor’s Degree in Sociology and Education from Tel Aviv University.
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