Sagit Mis
About Sagit Mis
Sagit Mis is a Clinical Trial Regulatory Specialist at Novocure with over 15 years of experience in regulatory affairs and quality control within the pharmaceutical industry.
Company
Sagit Mis currently works at Novocure as a Clinical Trial Regulatory Specialist. She joined the company in July 2018 and is based in the Haifa Area, Israel.
Title
Sagit Mis holds the position of Clinical Trial Regulatory Specialist at Novocure. Her role involves overseeing clinical trial regulatory processes to ensure compliance with industry standards and regulations.
Previous Experience at Teva Pharmaceuticals
Before joining Novocure, Sagit Mis worked at Teva Pharmaceuticals in various roles. From 2014 to 2018, she served as a Regulatory Affairs Associate, focusing on regulatory submissions and compliance for the Copaxone product. Prior to that, she was a Quality Control Analyst in the Copaxone Lab from 2008 to 2014, ensuring the quality control of Teva's pharmaceutical products.
Education and Expertise
Sagit Mis studied at Ben-Gurion University of the Negev, where she earned a Bachelor of Applied Science (BASc) in Materials Engineering from 1998 to 2002. She has over 15 years of experience in regulatory affairs and quality control within the pharmaceutical industry, as well as extensive expertise in materials engineering.
Background in Materials Engineering and Electron Microscopy
Sagit Mis has a substantial background in materials engineering and electron microscopy. She worked as an Engineer at the Electron Microscope Laboratory at Technion - Israel Institute of Technology from 2002 to 2006. Additionally, she served as a Materials Engineer in the R&D laboratory of Schieffer-Magam Industry in 2007.