کوشان فارمد

منتشر شده 4 سال پیش

سمت شغلی

شرکت

حقوق

آمار رزومه‌های ارسال شده

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 medical devices procedures - Familiar with 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 - Review documents as CTD, PMFs, to fulfill MOH requirement for registration - Familiar with TTAC portal of MOH - Review product printing materials, labeling, specification sheets with applicable regulations and policies

Requirements

Skills and Qualifications - Age: Maximum 35 years old - Education: Pharm.D. - Professional experience: Minimum 3 years in the field of Pharma (experience in multinational companies is a plus) - Skills Good communication and interpersonal skills Perfect command of English language (verbal, written and translation) Good MS Office proficiency (especially Excel and Word) Familiar with TTAC system Being a qualified pharmacovigilance professional is preferred Being a qualified person for medical devices is preferred - Traits: Hardworking, multitasking capability, team working, self-motivated, flexible, positive and active attitude, willing to take responsibility, enthusiastic about learning

Employment Type