Amir Agharezaee Email & Phone Number

Mainland, Pa

Analysis of raw materials of cosmetics and dietary supplements with a variety of methods including UV-Visible, KF, gravimetric analysis, wet chemistry.

Lee, Massachusetts, United States

• Analytical method development, transfer, and validation in cGMP environment.• Troubleshooting and maintenance of various analytical techniques including HPLC and GC and Empower software in cGMP environment for both small molecules and large molecules.• Setup and equipped of the Pharmaceutical and Dietary Supplements Laboratory from the ground up.• Experience in pharmaceutical industries and food, beverage, and pharmaceutical regulatory control laboratories.• Hands on experience with chemical synthesis and wet chemistry.• Hands on experience with cell culturing.• More than 6 years of work experience in pharmaceutical analytical laboratories in industry.• Willing to learn new skills and grow.

Albany, New York, United States

Albany, New York, United States

Albany, New York, United States

Qeshm, Iran

 Setup and equipping the Pharmaceutical and Dietary Supplements Laboratory from the ground. Hiring staff for the lab. Post Manufacturing Quality Control (PMQC) of domestic and imported pharmaceuticals and dietary supplements with a very diverse scope.

Tehran, Iran

Tehran

Tehran- Iran

Responsibilities:- Writing SOP- Quality control of raw materials of plant origin according to Pharmacopoeias or In-house methods. This included application of variety of analytical techniques, from classical methods of analysis to derivatization, extraction and preconcentration, followed by determination by GC, HPLC, UV-Visible spectrometry, electrochemical and colorimetric titration or gravimetric analysis.- Analysis of different physicochemical properties of pharmaceutical excipients, mostly by classical methods of analysis.- Quality control of finished products (variety of dosage forms).

Tehran, Iran

 Quality control of finished products and raw materials (RM) by HPLC including identification, assay and impurity determination tests according to United States Pharmacopoeia (USP), British Pharmacopoeia (BP), European Pharmacopoeia (EP), Japanese Pharmacopoeia (JP) and In-house methods. Method development of In-house methods of analysis for new products or updating the analysis methods of the then current products and their respective raw materials, Setup of analysis methods according to Pharmacopoeias for new products and RMs or when respective monographs in Pharmacopoeias were updated.

Master'S Degree, Organic Chemistry/ Medicine, 3.44

Master’S Degree, Analytical Chemistry

Research subject: Differential Pulse Anodic Stripping Voltammetric Determination of Lea d(II) by a Dimethylglyoxime Modified Sol-Gel.

Bachelor’S Degree, Applied Chemistry, 3.57