Azgor Miazi

Dynamic, highly driven scientist with expertise in laboratory testing, safety, and product validation gained over eight years of professional experience. Proven ability to oversee multiple concurrent ventures while maintaining strict adherence to research best practices. Excels in manipulating advanced instruments and equipment. Personable and energetic with the communication skills needed to build consensus on challenging initiatives.

Scientist - Amneal Pharmaceutical - Long Island, NY

(2022-08)

Perform testing of in-process and finished pharmaceutical products, including products on stability, according to written methods or compendial methods. Maintains laboratory record documentation (notebooks and computer-based).

Perform

Physical test, dissolution, Assay, CU, FT-IR, UV-Vis spectrophotometer, HPLC, among other instruments. Prepares volumetric test solutions following USP or in-house methods for wet chemical tests, standardizes such solutions. Document and report result as per established SOPs. Actively participates in and leads investigation of out of alert limit, out-of-specification laboratory results, when required.

• Work seamlessly across finished product, in-process, stability, and raw materials.
• Leverage mastery over HPLC (EDS, Waters, Shimadzu, and Agilent), UPLC, GC (Perkin Elmer, Agilent), dissolution units (Sotex and Distek automation, Ezfill), UV, PDA, RI, KF titration, particle size, FT-IR, TLC, blend uniformity, content uniformity and cleaning validation.

Quality Control Scientist - IBN SINA Pharmaceuticals Industry - Gazipur, Dhaka

(2017-05 - 2021-03)

Analysis of Raw materials according to USP and NF, Assay/purity determination of raw materials and finished products by TLC, Potentiometric titration, manual titration, or with other equipment like UV-Visible spectrophotometer, HPLC and AAS as required by SOPs. Performed water determination by Karl Fischer and Moisture determination by moisture analyzer. Preparation of Reagents, Test Solutions, Volumetric Solutions as well and standardize them according to USP.

Assisted with request for ordering laboratory supplies. Monthly checking of expiration date of laboratory reagents, separate them and take measures to destroy them. Preparation and standardization of various test solutions & volumetric solutions.

• Eliminated large backlog of batches waiting for release through efficient analytical work.

Quality Control Scientist - Greenland Pharmaceuticals LTD - Tongi, Dhaka

(2014-01 - 2017-04)

Analysis incoming Raw Materials, Finished Products as per compendial method and in house SOP. Preparation and standardization of various test solutions & volumetric solution. maintains laboratory record documentation (notebooks and computer-based). Administered 4 internal quality audits and assessed results to inform corrective action measures.

Created and revised procedures, checklists and job aids to reduce errors. Created and collaborated in implementation and maintenance of customer complaint log

• Mentoring new staff on proper lab techniques, safety protocols, and regulatory requirements for senior QC personnel, helping to build a culture of quality.

Master of Science - Pharmaceutical Sciences - University of Development Alternative (2017-12)

Bachelor of Science - Pharmaceutical Sciences - Southeast University (2013-07)

Associate of Science - Science - Safua Safaria Fazil Madrasha (2006-01)