OBJECTIVE:
Aspiring for a position in a pharmaceutical company which will give me the
opportunity to learn and apply scientific techniques in Quality Control
department.
Summary
. Experienced working in Laboratory environment following GLP
. Demonstrated analytical skills for analyzing release profiles using
HPLC, UV visible spectroscopy, USP
Type I & II dissolution apparatus.
. Mathematical modeling of dosage form by using Winnonlin as a part of
course work.
. Maintaining and organizing records, SOPs.
. Proficient in operating tablet press (Single and multiple press), Karl-
fisher, hardness tester and
Friability tester.
. Hands on experiencing with pH meter, disintegration tester, Brookfield
viscosity meter.
. Excellent written, oral and organizational skills.
. Experienced in preparation of Cream, Emulsion, Ointment and
Suspensions.
EDUCATION:
Long Island University, Brooklyn, NY .
May 2013
Master of Science in Pharmaceutics specialized in Industrial and Physical
Pharmacy
Relevant Course Work: Industrial pharmacy; Pharmaceutical Analysis;
Physical Chemistry; Advance Physical pharmacy; Advanced Bio-pharmaceutics
and Pharmacokinetics; Dosage Form Design; Controlled Release Systems;
Cosmetics and Dermatology; Mathematics Modeling
Parshvanath College of Pharmacy, Maharashtra, India
May 2010
Bachelor of Pharmacy (B Pharm)
Research and related experience:
Coxwain Pharma Pvt. Ltd. (India) Jun 2010 - Jan 2011
Quality Control Associate
? Analyze samples obtained from HPLC, GC, UV-VIS Spectrophotometer as per
the specifications
according to the SOPs.
? Write, review and maintain SOPs/Test Protocols/Methods of Analysis.
? Calibrate and maintain laboratory equipment such as pH meters, auto
titrators, weighing balances in
accordance with manufacturer recommendations.
? Perform disintegration and dissolution testing on solid dosage forms.
? Perform sample preparation procedures using a number of techniques such
as extraction, sonication,
solvent evaporation, dilution, and filtration.
? Perform algebraic calculations to quantify test results
? Highly experienced in working cGMP environment.
? Ensure a safe work environment in compliance with all safety policies and
procedures using the
appropriate tools and equipment for the task
Reine Chemicals Pvt. Ltd. (India) May - Aug 2009
Research Intern
? Assisted senior Pharmacist in Quality Assurance Department and Research
and Development
? Handled documentation records & performed QC test: dissolution, HPLC,
UV.
? Learned basic skills in Production Department
? Assisted in Drafting Drug Specifications
COMPUTER SKILLS: Very well acquired with Microsoft Excel, Word, Power
point, Windows, Surfing. (Literature search and
appropriate data organization)
SPECIALIZE SKILLS:
. Able to do work with, possesses excellent attitude and work ethic.
. Able to deal with people and manage things easily.
. Excellent interpersonal skill with the most loyalty, sincerity and
honesty.
REFERENCES: Available upon request