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Rabab AbdoRA
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Rabab Abdo

@rabababdo

I manage pharmaceutical, biologics, medical device, and cosmetics regulatory submissions.

Sudan
Message

What I'm looking for

I'm looking to contribute my regulatory affairs, quality assurance, and pharmacovigilance experience to pharmaceutical, biologics, medical device, or cosmetics registrations and compliance.

I'm supporting Amjad International LLC in Oman as a remote Regulatory Affairs Specialist and General Manager Assistant for cosmetics and medical products.

Previously at Almahgoub Pharmaceuticals, I reviewed and submitted manufacturer and CTD product files to Sudan's National Medicines and Poison Board, managed renewals, variations, safety reports, and shipment compliance.

At Shima Medical Co. and Luqman Medical Co., I coordinated registrations for pharmaceutical manufacturers, medical devices, and consumables, liaised with international manufacturers and regulatory authorities, and participated in audits and SOP preparation.

I'm a registered pharmacist with a Master's in Quality Assurance in Pharmaceuticals, experience in pharmacovigilance and GDP/GSP compliance, and published research on eCTD, medicine packaging artwork, and pharmaceutical regulatory protection.

Experience

Work history, roles, and key accomplishments

AL
Current

Regulatory Affairs Specialist and General Manager Assistant

Amjad International LLC

Mar 2025 - Present (1 year 6 months)

Serving as an authorized representative agent for Ferrari Professional, specializing in cosmetics and medical products.

AL

Regulatory Affairs Specialist

ALMAHGOUB PHARMACEUTICALS CO. LTD

Feb 2021 - May 2023 (2 years 3 months)

Communicated with national regulatory authorities and manufacturers to fulfill regulatory requirements. Reviewed and submitted registration files, ensured follow-up and renewal of registered products, and coordinated with supply chain for compliance with GDP and GSP.

SL

Head of Regulatory Affairs

SHIMA MEDICAL CO. Ltd

Jun 2018 - Jan 2020 (1 year 7 months)

Served as liaison between regulatory authority and international manufacturers. Reviewed and submitted product registration dossiers, assisted in preparing SOPs, and participated in audits.

LC

Regulatory Affairs Officer

LUQMAN MEDICAL CO.

Jan 2016 - May 2018 (2 years 4 months)

Examined conformity of registration documents, reviewed and submitted registration files for new manufacturers and medical devices, and followed up on regulatory renewals and safety documents.

UP

Trainee

Unimed Pharmaceuticals

Dec 2014 - Jul 2015 (7 months)

Worked as a trainee in the Quality Assurance Department.

Education

Degrees, certifications, and relevant coursework

Philadelphia University logoPU

Philadelphia University

Professional Training Program, Regulatory Affairs of Drugs and Medical Devices

Professional Training Program in Regulatory Affairs of Drugs and Medical Devices from Philadelphia University, Jordan, completed in 2025.

IU

Ibn Sina University

Master of Quality Assurance in Pharmaceuticals, Quality Assurance in Pharmaceuticals

Master of Quality Assurance in Pharmaceuticals from Ibn Sina University, Sudan, completed in 2016.

Ahfad University for Women logoAW

Ahfad University for Women

Bachelor of Pharmacy, Pharmacy

Bachelor of Pharmacy degree from Ahfad University for Women, Sudan, completed in 2009.

Tech stack

Software and tools used professionally

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