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
Requirements: B.Pharm degree mandatory
Experience as an Appointed Pharmacist mandatory
Proven experience in regulatory affairs, including new submissions, renewals, variations, labeling, and packaging components
Strong understanding of generic and innovative products
High level of accuracy, attention to detail, and excellent organizational skills
Stong English communication skills (written and verbal)
Ability to work independently, manage multiple priorities, and meet deadlines
Strong ability to work with digital systems and regulatory platforms
Excellent interpersonal skills and ability to collaborate with multiple stakeholders locally and globally
This position is open to all candidates.
