Job Description
-Preparing the forms and documents for new products to be sent to MOH -Ensuring compliance with Iran’s Ministry of Health regulations and guidelines -Keeping up-to-date with changes in regulatory legislation and guidelines -Writing comprehensible, user-friendly, clear Persian product information leaflets and labels -Translating the needed documents to be submitted to MOH -Familiar with contract manufacturing and under license manufacturing process and regulations -Being connected with raw material suppliers -Helping marketing department by preparing supporting documents required for physicians' scientific visit with the aim of persuading them prescribing our products -Reporting to: R&D Manager
Requirements
-BS or higher in Chemical sciences/ Master of Chemistry would be preferred -A good understanding of Iranian Drug regulatory and quality framework -Active, reliable, self-driven and motivated. -Hard working and honest -Good command of computer knowledge (MS. Office) -Able to work within a team, problem-solving spirit -Must be easily adapt to priority changes and able to work on numerous simultaneous projects to meet established timelines -Must be extremely detail-oriented and be able to work with minimal supervision -Requires strong oral and written communication skills. - Proven ability to remain calm while working against a deadline -Being familiar with CTD format, IDL and the procedure of TTAC -Ideal Age Range: 25 - 35 -Excellent knowledge of English
Employment Type
- Full Time
Job Category
Seniority
Details
Employment type
- Full Time
Job Category
Educations
Seniority
