לוח אפשרויות קריירה - הדרך החכמה להייטק

Serve as the primary point of contact with the Israeli Ministry of Health for all aspects of dossier registration and lifecycle management
Prepare and submit new drug registration applications (generic and innovative)
Manage submissions for renewals and variations
Review, prepare, and approve PILs and PPIs
Review, prepare, and approve packaging materials
Maintain full regulatory compliance throughout the product lifecycle
Collaborate closely with internal cross-functional teams, including Quality Assurance (QA), Pharmacovigilance (PV), Supply Chain (SC), and global regulatory counterparts
Support and lead regulatory projects and improvements across the organization