Job Description

Follow-ups with the Iranian Ministry of Health on files review and ensures timely submission of additional documentation requested in field of pharmaceutical, supplement and cosmeceutical products • Support all Regulatory Affairs activities in order to achieve and maintain registrations in compliance with all national and regional Regulatory and legal obligations. • Supervision of quality processes • Familiar and provision of SOPs • Gathering Pharmacovigilance and ADR reports • Develop professional relationships with MOH staff and proactively monitor relevant governmental bodies to identify changes in legislation/regulations • Annual product reviews and review of stability reports for compliance with Food and Drug Regulations • Review documents as CTD, PMFs, to fulfill MOH requirement for registration • Familiar with TTAC portal of MOH and material registration • Review product printing materials, labeling, specification sheets with applicable regulations and policies.