Master's student in Development of Drugs and Health Products with a strong pharmacy background, actively seeking a research internship focused on biologics formulation and drug delivery. Bringing hands-on experience in in vivo and in vitro research, quality assurance, and regulatory compliance to contribute to innovative pharmaceutical development.
Registration Staff
Ho Chi Minh City, Ho Chi Minh, Viet Nam
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Summary
Managed regulatory documentation for health supplement registration, ensuring full compliance with industry standards and quality protocols.
Highlights
Prepared and meticulously reviewed regulatory documentation packages for health supplement registration, ensuring 100% adherence to national guidelines.
Ensured stringent compliance with all regulatory and quality standards, facilitating timely product approvals.
Collaborated cross-functionally to gather necessary information, streamlining the documentation submission process.
Quality Assurance Specialist
Binh Duong, Binh Duong, Viet Nam
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Summary
Ensured product quality and process consistency within a pharmaceutical manufacturing environment through robust quality assurance practices.
Highlights
Maintained high product quality and process consistency within a pharmaceutical manufacturing environment, adhering to stringent GMP standards.
Participated actively in process validation and equipment qualification, directly contributing to enhanced formulation robustness and reliability.
Developed strong proficiency in technical documentation, ensuring reproducibility and fostering a quality-by-design mindset across operations.
Collaborated with production teams to identify and resolve quality deviations, improving overall manufacturing efficiency.
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Master's Degree
Development of Drugs and Health Products (M1)
Courses
Pharmaceutical Formulation and Drug Delivery Systems
Biotechnological and Biological Drugs
Inflammation and Disease Mechanisms
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Bachelor's Degree
Pharmacy
Grade: 7.05/10 (Good)
Published by
Ho Chi Minh City Journal of Medicine
Summary
Published research demonstrating the hepatoprotective and antioxidant effects of a novel herbal extract mixture against acetaminophen-induced hepatotoxicity in mice, contributing to pharmaceutical knowledge.
In Vivo Experimentation (Mice, PO, IV), Molecular Biology Techniques (PCR, ELISA), Antioxidant Assays (DPPH, Malondialdehyde Quantification), Experimental Design, Data Collection & Interpretation.
Regulatory Documentation, Health Supplement Registration, Compliance Standards, Quality Assurance (QA), Process Validation, Equipment Qualification, Good Manufacturing Practices (GMP), Quality-by-Design (QbD).
Drug Formulation, Drug Delivery Systems, Biotechnological Drugs, Biological Drugs, Pharmacology, Toxicology.
Microsoft Office Suite, Data Analysis (R - Beginner).
Self-directed Learning, Team Collaboration, Technical Documentation, Reproducibility.
Department of Pharmacology, Faculty of Pharmacy, University of Medicine and Pharmacy at Ho Chi Minh City, Vietnam | Mobile: (+84) 908 683 080 | Email: hongtuoi@ump.edu.com
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Summary
Graduation dissertation project investigating the therapeutic potential of a herbal extract mixture against acetaminophen-induced hepatotoxicity.