Regulatory Affairs Specialist

Confidential - Egypt - Giza
  • Submission and follow-up of registration & re-registration files for the company’s product.
  • Preparation & Follow-up of files submission to various committees until receiving final approval.
  • Review & Submission of files & samples to EDA labs ensuring sourcing of analytical requirements  and following-up the analysis until receiving final conformity
  • Working closely with the department manager in the process of releasing finished products, imported raw materials, imported research and development samples and imported packaging materials.
  • Revising final outer and inner packs data & issuing approvals from EDA. and revising final films from printing houses.
  • Pre-formulation research for new pharmaceutical products.
  • Applying the company policies and work for achieving its goals according to the ethics, rules & regulations.

Bachelor’s degree pharmacy, veterinary medicine or science.Experience 2 years in dietary supplements, herbal medicines and cosmetics registration.
Post date: 10 April 2025
Publisher: Wuzzuf .com
Post date: 10 April 2025
Publisher: Wuzzuf .com