Regulatory Affairs Specialist, Israel
Core
Prepare registration portfolios, submissions, renewals, and variations for pharmaceutical products while ensuring compliance with regulations and managing packaging and leaflets.
Role type
Regulatory Affairs Specialist (Pharmaceuticals)
Builds
Regulatory dossiers and submission packages for pharmaceutical products
Domain
Pharmaceuticals / Healthcare
Required skills
Regulatory submission preparation, dossier maintenance, stakeholder communication (Ministry of Health), document review, packaging design, manual writing
Preferred skills
None stated
Technologies
Microsoft Office (Outlook, PPT, Word, Excel)
Responsibilities
Prepare all types of submissions (products, renewals, variations, leaflets, packaging); Maintain up-to-date product regulatory dossier; Contact Ministry of Health and international partners; Conduct regulatory and document checks
Seniority
Mid-level, hands-on IC
