Pharma Regulatory Affairs Officer
Confidential Company
Employer Active
Posted 2 hrs ago
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Experience
1 - 2 Years
Job Location
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
Company Industry
Keywords
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Confidential Company