Zarana Vadaliya

+1-516-***-**** ad0cs9@r.postjobfree.com https://www.linkedin.com/in/mayank-vadaliya-7a2821133 EDUCATION

Long Island University Brooklyn, NY

Master In Drug Regulatory Affairs Sep. 2023 – Current A-one Pharmacy college, Ahmedabad (Gujarat Technological University) Gujarat, India Master Of Pharmacy in Pharmaceutical Quality Assurance Aug. 2017 – Dec 2019 A-One Pharmacy College, Ahmedabad (Gujarat Technological University) Gujarat, India Bachelor Of Pharmacy Aug. 2013 – Jul 2017

EXPERIENCE

Management Trainee in QC, QA And Production Department June. 2017 – Sep 2017 ICPA Health Products Gujarat, India

• Involved in inspecting and testing products or processes to ensure they meet quality standards.

• Maintaining quality systems and processes

• Responsible for ensuring that production operations run smoothly and efficiently Work As a PHARMACIST

Aastha Pharmacy Store Mar 2020-May 2021 Gujarat, India Aastha medicines store May 2021-July 2023 Gujarat, India

• Accurately dispense prescription medications to patients, ensuring correct dosages and labeling.

• Verify the appropriateness of medication orders, checking for potential drug interactions and allergies.

• Provide medication counseling to patients, explaining proper usage, potential side effects, and any precautions.

• Maintain an organized and efficient inventory of pharmaceuticals.

• Monitor medication stock levels, order supplies, and manage pharmaceutical inventory.

• Stay current with developments in pharmacology, pharmacy regulations, and healthcare trends through ongoing education and training.

• Implement quality assurance programs to maintain high standards of pharmacy practice. PROJECTS

Quantitative Comparison and Validation of Standard and Generic Drugs Gujarat Technological University Aug. 2018 – Dec 2019

• Conducted an in-depth quantitative analysis and validation study comparing standard and generic drugs containing Paracetamol, Aceclofenac, and Serratiopeptidase using the RP-UPLC (Reversed-Phase Ultra-Performance Liquid Chromatography) method.

• Validation Parameters: Executed comprehensive validation procedures, including Linearity and Range, Specificity, Accuracy, and Precision, to ensure the reliability and compliance of the analytical method.

• Impact: This project contributed to the pharmaceutical quality control process by providing a robust analytical method for assessing the equivalence of generic and standard drugs, ensuring patient safety and regulatory compliance.

SKILLS

Time Management

Communication

Inventory Management

Pharmaceutical Science

Decision Making

Pharmacokinetics and Pharmacodynamics

Drug interactions and contraindications electronic health records utilization Market Research and compliance with state pharmacy laws

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