Pharmaceutical Product Registration Expert

5 days ago


Jeddah, Makkah Province, Saudi Arabia Nahdi Medical Co. Full time
Job Overview

We are looking for a seasoned Regulatory Affairs expert to lead our SFDA Registrations Department in Saudi Arabia. As a critical member of our team, you will oversee the registration and approval process of pharmaceutical products, ensuring compliance with SFDA regulations.

Your Key Responsibilities:
  • Lead the registration and approval process of pharmaceutical products
  • Cultivate strategic relationships with SFDA officials to ensure timely and compliant product registrations
  • Develop and implement efficient registration timelines to meet business objectives
  • Maintain knowledge of regulatory changes and their impact on the company's areas of interest
  • Ensure compliance with all relevant regulatory guidelines and standards

As part of our dynamic team, you will contribute to driving business growth through effective regulatory strategies and processes.

Requirements

A Bachelor's degree in Pharmacy or a related field is required, along with at least 8 years of experience in regulatory affairs, specifically in the Drugs and Health/Herbal sectors. Excellent communication skills, analytical abilities, and knowledge of pharmacopoeias are also essential.



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