Haviva Choufane

Haviva Choufane is a seasoned regulatory affairs professional with extensive experience in managing regulatory strategies and compliance for biological products. Currently serving as Sr. RA Specialist and CMC Project Lead at Syqe Medical since June 2022, Haviva has previously held positions including Regulatory Affairs & QA Consultant at IQVIA and Senior Regulatory Affairs CMC Program Lead at Omrix Biopharmaceuticals. Responsibilities have included assessing and classifying changes per FDA, EMA, and IMOH regulations, submitting post-approval changes, overseeing lifecycle submissions, and managing regulatory projects across multiple manufacturing sites globally. Haviva's background also includes validation and quality assurance expertise gained as a Process Technology Scientist at Aliquo Pharma Consulting. Haviva Choufane holds a Bachelor of Science in Chemical Engineering from SCE - Shamoon College of Engineering.