Freelance Regulatory Affairs Consultant – Pharmaceutical Industry

apartmentTheSay placeDubai calendar_month 

Job description / Role

Employment: Contract

We are looking for a Senior Regulatory Affairs Consultant on a freelance basis to support the registration and regulatory compliance of pharmaceutical products across the UAE and other GCC countries. The ideal candidate will have deep expertise in GCC regulatory frameworks and strong working relationships with health authorities, particularly the Ministry of Health (MOH) in the region.

Key Responsibilities:
  • Oversee and manage the end-to-end registration process for pharmaceutical products in the UAE and GCC markets.
  • Provide expert guidance on local and regional regulatory requirements and ensure full compliance with current laws and guidelines.
  • Support our RA team in liaising with health authorities, particularly MOH in the UAE and other GCC countries.
  • Advise internal teams and clients on regulatory strategy, dossier preparation, and submission timelines.
  • Monitor regulatory changes and provide impact analysis and action plans accordingly.
  • Support in responding to queries and deficiencies raised by regulatory bodies in a timely and professional manner.

Requirements:

Priority - URGENT
Requirement - Permit to work as Freelance
  • Experience: 7 to 10 years of hands-on experience in Regulatory Affairs within the pharmaceutical industry, with a strong focus on the UAE and GCC countries.
  • Proven track record of successful and timely product registrations and renewals in the region.
  • In-depth knowledge of current regulatory laws, guidelines, and procedures in the UAE and other GCC countries.
  • Experience working directly with MOH and familiarity with their systems and expectations.
  • Strong communication, problem-solving, and project management skills.
  • Ability to work independently and deliver high-quality results on time.

About the Company

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