Summary
Overview
Work History
Education
Skills
LANGUAGES
Timeline
Generic

ASEEL ALQUDAH

Amman

Summary

Strongly reliable and focused Regulatory Affairs Specialist with great depth and breadth of experience in Medicinal Products, Medical Devices, Herbal Products, Food Supplements and Cosmetic Products registration. Effective independent worker as well as excellent coordinator with other members of a regulatory affairs team.

Overview

11
11
years of professional experience

Work History

Regulatory Affairs Professional and Consultant

Radex Consultation Office
04.2020 - Current
  • Analyzes market trends to provide actionable insights that enhanced client decision-making processes.
  • Develops comprehensive project plans, ensuring alignment with client goals and expectations.
  • Coordinates with clients to identify needs, delivering tailored consulting services that drove satisfaction.
  • Evaluates client needs and expectations, establishing clear goals for each consulting engagement.
  • Collaborates with cross-functional teams to successfully deliver comprehensive solutions for clients.
  • Analyzes data sets to identify trends and opportunities for process improvements within client organizations.

Regulatory Affairs Supervisor

Sana Pharma
04.2017 - 02.2020
  • Review all regulatory submission materials to ensure timeliness, accuracy, comprehensiveness, and compliance with regulatory standards.
  • Communicate regulatory information to multiple departments and ensure that information is interpreted correctly.
  • Prioritizing and Planning Work and Activities.
  • Guiding, Directing, and Motivating Subordinates.
  • Making Decisions and Solving Problems- Analyzing information and evaluating results to choose the best solution and solve problems.
  • Maintain current knowledge of regulatory standards.
  • Implement Quality Assurance systems.

Regulatory Affairs Officer

Sana Pharma
03.2014 - 03.2017
  • Do necessary paperwork and documentation processes.
  • Gathering data and preparation of technical dossiers.
  • File submission to JFDA, renewals as needed.
  • Keep track of regulatory submissions at JFDA.
  • Attend continuing education courses to keep updated with changing RA policies.

Education

Professional Diploma - Regulatory Affairs of Drugs and Medical Devices

The Applied Science Private University
11.2018

Mini-MBA Program - undefined

Change Zone - Accredited Training & Consultation Services (IACET)
12.2016

Bachelor of Science (B.SC.) - Pharmacy

The University of Jordan
06.2013

Scientific track high school - undefined

Iskan Yajouz Secondary School
06.2008

Skills

  • Proficient Computer Skills
  • Communication Skills
  • Detail Oriented
  • Team Leadership
  • Time Management

LANGUAGES

Arabic: Native.
English: Excellent.

Timeline

Regulatory Affairs Professional and Consultant

Radex Consultation Office
04.2020 - Current

Regulatory Affairs Supervisor

Sana Pharma
04.2017 - 02.2020

Regulatory Affairs Officer

Sana Pharma
03.2014 - 03.2017

Mini-MBA Program - undefined

Change Zone - Accredited Training & Consultation Services (IACET)

Bachelor of Science (B.SC.) - Pharmacy

The University of Jordan

Scientific track high school - undefined

Iskan Yajouz Secondary School

Professional Diploma - Regulatory Affairs of Drugs and Medical Devices

The Applied Science Private University
ASEEL ALQUDAH