مدیر امور تنظیم مقررات

پارس گیتا دارو تهران

بیش از یک ماه منتشر شده

Job Description

  • Register the source and obtain IRC of raw materials.
  • Complete drug CTD for all pharmaceutical forms.
  • Complete PMF of complementary products and natural products.
  • Add pharmaceutical products to the IDL list.

Requirements

  • Full familiarity with regulatory affairs.
  • Full familiarity with the rules and regulations of the Food and Drug Organization.
  • Full familiarity with the TTaC system.
  • Complete familiarization with the process of obtaining a license for complementary medicinal products and medical supplements.
  • Full familiarity with the process of issuing a license for the opening and clearance of imported raw materials.
  • Getting to know the laws governing the administration of pharmaceutical supplies.
  • Previous records in the field of regulatory and registration of products.
  • Fluent in English.
  • Teamwork spirit.
  • Ability to manage time in the product registration process.
  • Previous experience in preparing product registration documents.

Employment Type

  • Full Time

Details

امریه سربازی

Employment type

  • Full Time

برای مشاهده‌ی شغل‌هایی که ارتباط بیشتری با حرفه‌ی شما دارد،