Abdulrazak Moosa

Professional Summary
Motivated professional with a Master's in Pharmaceutical Analysis and a strong foundation in analytical and quality control practices within GMP/GLP-compliant environments. Skilled in advanced techniques such as HPLC, LC-MS/MS, FTIR, UV-Vis, and GC, with hands-on experience in method development and stability studies. Demonstrates a proven ability to deliver accurate and reliable results, supported by research experience in the degradation behavior of antibiotics in space-like conditions. Adept at problem-solving, teamwork, and maintaining compliance with regulatory standards. Enthusiastic about contributing to innovative projects and driving excellence in analytical science.

Senior Research Fellow 
Amrita Institute of Medical Sciences, Kochi, India
February 2023 – August 2023

• Collaborated on clinical research projects involving pediatric cardiology, contributing to data collection and analysis for improved treatment outcomes.
• Coordinated with interdisciplinary teams to ensure timely and efficient completion of research objectives.
• Maintained meticulous records, adhering to strict regulatory and institutional guidelines.

Clinical Pharmacist – General Medicine
Amrita Institute of Medical Sciences, Kochi, India
September 2021 – February 2023

• Provided evidence-based pharmaceutical care, optimizing medication therapy for patients in a multidisciplinary team.
• Conducted medication reconciliation and patient counseling, improving adherence and therapeutic outcomes.
• Contributed to drug utilization reviews and reported adverse drug reactions, enhancing patient safety.

MSc Research Project – Pharmaceutical Analysis
Kingston University, London, UK
September 2023 – September 2024

• Conducted an extensive stability study on antibiotics exposed to gamma radiation and photodegradation to evaluate their degradation patterns and stability under space-like conditions.
• Designed and implemented robust analytical methods to quantify degradation products, ensuring accuracy and reproducibility.
• Utilized advanced analytical tools such as HPLC and LC-MS/MS to identify and characterize degradation impurities, enabling a deeper understanding of compound behavior.
• Performed method validation and optimization to ensure compliance with ICH guidelines for analytical quality and reliability.
• Prepared detailed reports of experimental findings, contributing to insights for potential applications in pharmaceuticals for extreme environments.
• Demonstrated expertise in managing laboratory workflows, troubleshooting instrumentation, and maintaining adherence to GMP and GLP standards.