Quality Control Product

NISHMA P. PATEL

*** ********* ***

Salinas CA ***06

Email : *************@*****.**.**

Contact No. : 831-***-****

OBJECTIVE

Seeking a position in Pharmaceutical industry that will consider skills, knowledge and past experience as an additional benefit for the growth of company

COMPETENCIES

Over 2 years of experience in Pharmaceutical industry in Analytical Research and Development

Actively participated in development of ANDA and NDA analytical testing methods, authoring validation protocols, generating reports and smooth method transfers

High efficiency to operate EMPOWER, Empower for HPLC

Excellent command in using TLC, HPLC, HPTLC, IR UV, Dissolution Apparatus, USP I, II and USP IV

Capable of raw material testing and drug testing validation and assays.

Capable of handling multiple assignments high pressure and consistently meeting tight deadlines

Self-motivated, detail-oriented, cooperative team player, eager to learn

Excellent interpersonal and communication and technical writing skills

Articulate Presentation skills

COMPUTER SKILLS. MS office, MS excel.

EDUCATION

Master of Pharmacy in Pharmaceutical Analysis June 2015

Gujarat Technological University, Gujarat, India

Bachelor of Pharmacy June 20013

Gujarat Technological University, Gujarat, India

EXPERIENCE

Developed analytical method for Finished product for solid formulation

Reported and discussed analytical results and conclusions both orally and in writing.

Developed particle size measurement method for finished product

Performed Dissolution of finish product by using USP I and II

Operated HPLC, IR spectrometer, Dissolution Apparatus USP type II and IV

Performed Assay and RS determination of Finished Product, Stability samples

Supported API evaluation, product characterization by using viscometer, colorimeter

Kept record of all data on regular basis

Calibrated lab equipment

Actively involved in development of dissolution process for low solubility finished product

Authored SOPS for lab equipment operation, handling and calibration

INTERNSHIP

Tuton Pharmaceutical Pvt. Ltd., India December 2012- May 2013

Production and Quality control trainee

In Production: Batch wise Preparation of Tablets and Capsules,

Performed Dissolution,Assay and RS determination,and content uniformity test

Calibrated lab equipment and maintained

Authored SOP for cleaning and calibration of lab equipment

PUBLICATION

" Liquid Chromatographic Method for simultaneous Quantification of Alprazolam and Mebeverine in Pharmaceutical dosage form" in INDIAN JOURNAL OF PHARMACEUTICAL SCIENCE in June 09, 2015.

" Thin layer Chromatography Method for the Simultaneous quantification and stability testing of Alprazolam and Mebeverine in their combined Pharmaceutical dosage form" in Journal of Taibah University for Science in September 07, 2015.

Reference : Available upon Request

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