Sibel Saydan is a Regulatory Affairs Executive at TRPHARM, with experience in various regulatory roles in the pharmaceutical industry, including a position as Regulatory Science Senior Specialist at Bristol Myers Squibb and as an International Markets Senior Regulatory Affairs Specialist at DEVA Holding A.Ş. Sibel has also held roles as a Senior Regulatory Affairs Specialist at Neutec Pharmaceuticals and completed internships focused on quality control and production in both the beer and cement industries. Sibel's academic background includes an Engineer's degree in Chemical Engineering from Ege University, where involvement as a board member and R&D commission leader was also notable.
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