Eesha Maranganti
Asuntos Regulatorios en Farmacia en Northeastern University
Canadá
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Industrial training en Reddy’s laboratories
Redes sociales
No se agregaron enlaces sociales
Experiencia
Reddy’s laboratories
Industrial training
June 2022 - July 2022
Contributed to quality assurance by assisting in setting chemical ranges, observing product testing protocols, and ensuring compliance
with regulatory standards.
• Analyzed and documented quality control processes, strengthening knowledge of Good Manufacturing Practices (GMP) and Standard
Operating Procedures (SOPs).
• Acquired practical knowledge of pharmaceutical machinery and safety protocols, critical for compliance in a regulated environment.
• Supported QA and QC teams on product assessments, reinforcing compliance monitoring skills within an industrial setting.
Surya Hospitals
Hospital training
September 2021 - October 2021
Organized and supported inventory by categorizing drugs based on therapeutic roles, enhancing knowledge of drug classifications and
regulatory requirements.
• Dispensed medications per prescriptions, ensuring accuracy and adherence to safe dispensing practices.
• Educated patients on medication purpose, potential side effects, and usage, emphasizing patient safety.
• Conducted and documented case studies, improving skills in compliance documentation and patient care for regulatory settings.
Educación
Asuntos Regulatorios en Farmacia
Northeastern University
Graduado en 2024
Certificaciones y Distintivos
No se agregó certificaciones o distintivos
Proyectos
Development of Anti-Hypercholesterolemia Drug Using Cinnamon and Nigella Sativa
•https://www.sysrevpharm.org/articles/a-brief-report-on-hyperlipidemia-and-its-inducing-models-102080.htmlContributing research student
I worked on a research project focused on exploring the anti-hypercholesterolemia potential of natural ingredients, specifically a combination of cinnamon and Nigella sativa. My role involved conducting experiments to evaluate their pharmacological effects, carefully documenting and analyzing results while following Good Laboratory Practices (GLP). I also presented the findings to my research team, which helped me strengthen my communication skills and gain valuable experience in scientific and regulatory documentation. This project deepened my understanding of natural product research and its application in developing potential treatments.
Idiomas
Inglés
Profesional
Habilidades
Project Management
Risk Management
Communication - Keeping a Customer informed of Progress and advising on Workarounds
Good Manufacturing Practices (GMP)
SOPs
FDA Guidelines
IND
Clinical Trial Management System (CTMS)