Summary
Arabian Ethicals, a member of Ghobash Group, is a UAE pharmaceutical distributor with offices and warehouses in Dubai and Abu Dhabi. The Regulatory Affairs Officer manages registrations for pharmaceutical, veterinary and medical products, reviews regulatory documentation, and coordinates with authorities and logistics teams to secure approvals and import permits. The role also supports product launches, maintains registration dossiers, handles quality queries and complaints, and carries out pharmacovigilance activities, including SOP preparation and staff training. A bachelor’s degree or higher is required; a pharmacy background is preferred but not essential.
The posting
As published on ghobash.com. Pulled from the employer's site and shown as they wrote it.
Company Description
Arabian Ethicals, a member of the Ghobash Group, was formed in the early 1970’s as a pharmaceutical distributor. Over the years, it has expanded its core business to become one of the leading pharma distributors in the UAE, but also diversified into adjacent segments such as veterinary, nutrition, and consumer products. Today, Arabian Ethicals is the trusted partner of global brands such as Merck-Serono, Sandoz, Acino, Nuk, and many others. With offices and warehouses in Dubai and Abu Dhabi and a team of over 120 dedicated employees, Arabian Ethicals is distributing to all major pharmacies, hospitals, supermarkets and other retail outlets across the country. Making an impact in the daily lives of the people in UAE, Arabian Ethicals serves with passion and aims to deliver through positive advancements in the healthcare industry. Touching Lives Everyday
Job Description
The job holder is responsible for management and facilitation of registration related to Pharmaceutical, Veterinary and Medical. She/he builds relationship with regulatory authorities; coordinates with Logistic teams to provide regulatory input in order to obtain timely regulatory approvals for the products; handles quality related queries / complaints; and stays updated on regulatory aspects pertinent to business development.
Key Responsibilities:
Complete registration formalities for Pharmaceutical, Veterinary and Medical
- Review regulatory documentation and technical product information
- Provide regulatory support for portfolio of products
- Establish and update registration database in the company
- Update licenses and collect information on registration instructions and regulations
- Provide and complete forms need in registration
Complete forms and requests originating from government agencies (DM)
- Carry out all subsequent follow up and pricing negotiations necessary to obtain the approval
- Checking all import permits
Maintain contact with regulatory authorities
- Communicate with regulatory bodies in DM & MOH to facilitate successful product launch.
- Establish healthy & effective relationship with all concerned personnel at DM.
Provide the Logistic teams with regulatory input in order to obtain timely regulatory approvals for the products as part of the product development planning
- Update Logistic team on products for shipment.
- Ensure approval of import permits by DM.
Deal with quality related questions and complaints
- Follow up and update all existing registration dossiers & handling minor change variations that crop up from time to time
- Ongoing visits and intensive call to all concern people
- Timely accurate solutions to all complaints
Perform Pharma co-vigilance activities
- Prepare pharma co-vigilance SOPs as required by our principals.
- Train the company staff as per the SOPs.
- Follow up for any reported safety case.
- Providing required documentation to principals during occasional PV audits.
Qualifications
Bachelors Degree or Higher
Additional Information
Pharmacy background is preferred but not essential