کوشان فارمد

منتشر شده 5 سال پیش

Job Description

-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

Employment Type

  • Full Time

Details

Employment type

  • Full Time

Educations

برای مشاهده‌ی شغل‌هایی که ارتباط بیشتری با حرفه‌ی شما دارد،