Summary
Overview
Work history
Education
Skills
AWARDS & SCIENTIFIC PARTICIPATION
VOLUNTEER EXPERIENCE
PUBLICATIONS
Certification
Timeline
Generic
May Alzeer , MSc.

May Alzeer , MSc.

Riyadh,Saudi Arabia

Summary

Quality Control Specialist with proven experience in pharmaceutical quality systems and regulatory compliance. Skilled in implementing and maintaining quality standards including ISO requirements and Good Manufacturing Practices (GMP). Experienced in documentation control, Good Documentation Practices (GDP), and supporting deviation handling and continuous improvement processes. Actively contributed to regulatory processes, including coordination and documentation preparation for Saudi Food & Drug Authority (SFDA) accreditation.

Overview

5
5
years of professional experience
1
1
Certification

Work history

Product Specialist

STADA (Line: Dermatology)
2025.02 - 2025.08
  • Responsible for top-tier private hospitals in Riyadh and major pharmacy chains including Nahdi and Al-Dawaa.
  • Leading the dermatology product line and ensuring high visibility and availability across.
  • Maintaining strong partnerships with pharmacy purchasing departments and medical institutions.

Quality & Operations Executive

Med sea company
2023.10 - 2025.02

(Commercial Drug Warehouse) | 2022 – 2025

• Managed pharmaceutical operations including procurement coordination and client interactions within healthcare sector
• Ensured compliance with pharmaceutical quality standards across procurement and distribution processes
• Reviewed product specifications and verified alignment with regulatory and quality requirements
• Managed documentation in accordance with Good Documentation Practices (GDP)
• Monitored product quality, identified deviations, and reported discrepancies for corrective action
• Participated in supplier evaluation and product acceptance processes
• Supported implementation of quality procedures while maintaining daily operational responsibilities
• Collaborated with internal teams to ensure alignment between business operations and quality standardsregulatory expectations and quality standards

Product Specialist

Tabuk Pharmaceutical Company
2020.10 - 2022.08



• Maintained excellent relationships with procurement departments across assigned hospitals
• Conducted scientific presentations for physicians and healthcare professionals on drug mechanisms of action, proper usage, dosage, and safety profiles
• Provided detailed explanations of adverse effects and ensured safe and effective product use
• Reported observations and potential issues to internal teams to support product monitoring and continuous improvement
• Achieved 146% of sales target in the first year

Education

Master of Science - Quality Control

Prince Sattam Bin Abdulaziz University
Riyadh
01/2020 - 06/2022

Bachelor of Pharmaceutical Sciences - undefined

Riyadh Elm University
Riyadh
1 2013 - 1 2019

Skills

Good Documentation Practices (GDP)

Regulatory Compliance & Quality Standards

Deviation Handling & Root Cause Analysis

CAPA (Corrective and Preventive Actions)

SOP Implementation & Process Standardization

Audit Support & Quality Inspection

Documentation Review & Quality Reporting

HPLC-UV Method Development & Validation
Analytical Method Validation & Verification
Instrumentation: HPLC, GC, FTIR, UV-Vis Spectroscopy
Data Analysis & Interpretation of Analytical Results
Quality Control Testing & Laboratory Procedures

AWARDS & SCIENTIFIC PARTICIPATION

First Place – Prince Sattam Bin Abdulaziz University Award for Research and Innovation (All Disciplines), Poster Presentation – College of Pharmacy, King Abdulaziz University, Participant – Mohammed Said Tamer Chair Award for Best Scientific Poster

VOLUNTEER EXPERIENCE

King Faisal Specialist Hospital and Research Centre, Research Volunteer, Riyadh, Saudi Arabia, Supported ongoing clinical and pharmaceutical research projects within the research centre., Assisted in data collection, documentation, and regulatory preparation for study., Collaborated with regulatory teams in communication and document submission related to the Saudi Food & Drug Authority (SFDA)., Gained practical experience in regulatory compliance, ethical approvals, and research coordination processes.

PUBLICATIONS

  • Alzeer, M. A., et al. Pelargonium sidoides root extract: Simultaneous HPLC separation, determination, and validation of selected biomolecules and evaluation of SARS-CoV-2 inhibitory activity.
  • Pharmaceuticals
  • 15(10), 1184, Oct 2022. Impact Factor: 5.215
  • Alzeer, M. A., et al. Anti-quorum sensing and anti-biofilm activity of Pelargonium x hortorum root extract against Pseudomonas aeruginosa: Combinatorial effect of catechin and gallic acid.
  • Molecules
  • 27, 7841, Nov 2022. Impact Factor: 4.927 (Q2)

Certification

• Pharmaceutical Good Manufacturing Practice (GMP) Training
• ISO 9001:2015 Internal Auditor Certification
• ISO 17025: Laboratory Quality Management Systems

• Quality Assurance in Pharmaceuticals
• CAPA & Deviation Management
• Good Documentation Practices (GDP)

Timeline

Product Specialist

STADA (Line: Dermatology)
2025.02 - 2025.08

Quality & Operations Executive

Med sea company
2023.10 - 2025.02

Product Specialist

Tabuk Pharmaceutical Company
2020.10 - 2022.08

Master of Science - Quality Control

Prince Sattam Bin Abdulaziz University
01/2020 - 06/2022

Bachelor of Pharmaceutical Sciences - undefined

Riyadh Elm University
1 2013 - 1 2019
May Alzeer , MSc.