Pharma Regulatory Affairs Officer

Confidential Company

Employer Active

Posted 2 hrs ago

Experience

1 - 2 Years

Education

Bachelor of Pharmacy, Master of Pharmacy(Pharmacy)

Nationality

Any Nationality

Gender

Any

Vacancy

1 Vacancy

Job Description

Roles & Responsibilities

An International pharmaceutical company based in HQ in Dubai is looking to appoint an officer in its regulatory affairs department. The candidate should be a Pharmacist preferably with postgraduate studies in any scientific field, fluent in English and has at 1-2 years’ experience in registration of medicines. MOH license is mandatory and knowledge in Pharmacovigilance would be a plus.



Desired Candidate Profile

Job Responsibilities -

1. Prepare and submit regulatory dossiers: Compile, review, and submit documentation for the registration and renewal of pharmaceutical products in compliance with UAE Ministry of Health (MOH) guidelines.


2. Liaise with health authorities and internal teams: Act as the primary contact for regulatory communications, ensuring timely responses to inquiries and coordination between departments.


3. Maintain regulatory compliance and documentation: Ensure all product registrations, variations, and updates are accurately recorded and comply with local and international regulations.


4. Support Pharmacovigilance activities: Assist in monitoring, reporting, and documenting adverse drug reactions and safety updates, contributing to product safety and compliance.


5. Stay updated on regulatory changes and industry standards: Track evolving MOH regulations and global pharmaceutical standards to ensure proactive compliance and strategic planning.




Qualifications -

  • Bachelor’s degree in Pharmacy (mandatory); postgraduate studies in a scientific field preferred A solid academic foundation with advanced knowledge in pharmaceutical sciences or related disciplines.

  • Valid UAE MOH license Required for legal practice and regulatory submissions within the UAE.

  • 1–2 years of experience in pharmaceutical registration Hands-on experience with regulatory submissions and product lifecycle management.

  • Fluency in English (written and spoken) Essential for clear communication with health authorities and multinational teams.

  • Knowledge of Pharmacovigilance practices Familiarity with drug safety monitoring and reporting is a valuable asset.

Employment Type

    Full Time

Department / Functional Area

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Confidential Company