-Assist all regulatory affairs activities in order to achieve and maintain registration in compliance with all national and legal obligations
-Expand and facilitate relations with key authorization and organizations such as MOH and FDO
-Ensuring compliance with MOH regulations
-Preparing CTDs and related documents submitting to MOH
-Writing comprehensible, user-friendly, clear product information leaflets and labels
-Studying scientific and legal documents
-Outlining requirements for labeling storage and packaging
-Plan and manage all assigned projects with maximum efficiency
Requirements
-Minimum of 2 years of experience in related fields
-Pharmacist (Pharm D)
-Great command of written and spoken English
-Ability to work in a team
-Familiar with dossier and CTD format
-Familiar with registration process based on Iran regulation
-Familiar with the international pharmaceutical guidelines and pharmacopeia
-Excellent communication skills
-Good command of computer skills (MS Office)
-Problem solving
-Continuously follow-up skills