Resume of Dipa Panzade, P.Pharm./ QA/QC, Analytical Seciences

Dipa Panzade

**** ******* **** *****, ***** City, IA 50401

641-***-**** **********@*****.***

PROFILE

. Experience as a Quality Control Analyst and Quality Assurance Associate

. Reviewed all calibration, preventative/corrective maintenance and

qualification data in accordance with SOP, cGMP and regulatory guidelines

. Knowledge of USP and ICH guidelines

. Developed new analytical method for APIs and finished product

. Having sound knowledge of Millennium32 (data processing software for

HPLC)

. Experience in performing microbial tests

. Computer literate in Microsoft Office. Knowledge of LIMS

. Self-confident and expert in the performance of professional

responsibilities

. Able to work both as a team leader and a team member

. Strong interpersonal, communication, organizational and analytical skills

. Excellent technical and trouble shooting skills

. Ability to multi-task, self-motivated and work well under pressure to

meet deadlines

RELEVANT EXPERIENCE

Scientist 2006-2007

Caliper Life Sciences, USA

. Supported development and validation of analytical testing procedures for

API and drug products using APW and TPW for HPLC and UV methods.

. Supported service department for resolving customer complaints

. Actively supported quality assurance department for new application

developments

. Kept testing specifications current with applicable compendia changes

. Provided active feedback for quality improvement to stay competitive

with cutting edge technology

Quality Assurance Associate 2002-2005

Dextran Products Limited, Canada

. Assisted in writing, approval, distribution, revision and deletion of

SOPs, Technical manuals and other related documents

. Reviewed and approved or rejected procedures and specifications, product

changes, raw materials, packaging materials, in-process materials and

product batches

. Ensured the work performed is in compliance with SOP's, GDP, cGMP,

Technical Manuals, established safety standards and regulatory

requirements

. Reviewed all calibration, preventative/corrective maintenance and

qualification data in accordance with SOP, cGMP and regulatory guidelines

. Investigated and taken required actions for any out of specification

results

. Assisted in the development, implementation and maintenance of quality

systems in lab

. Performed revision and validation of methods as per USP and ICH

guidelines

Dipa Panzade 641-***-****

Page 2

R&D/ QC Analyst 2002-2005

Dextran Products Limited, Canada

. Worked independently in R&D lab, developed new HPLC methods for different

products

. Performed analysis on automated laboratory instruments such as HPLC, pH

meter, polarimeter, Brookfield viscometer, UV-Visible spectrophotometer

. Prepared test samples and performed analysis of APIs, in-process and

finished products samples in accordance with SOPs and cGMP requirements

. Calibrated laboratory equipments as per technical manuals (TM) and SOPs

. Revised previous SOPs as per technical manuals (TM) and pharmacopoeias

. Documented and reported results as per established SOPs following cGMP

and GDP guidelines

. Analyzed drug substances by Gel Permeation Chromatography

. Ordered necessary supplies and reagents

Research Associate 2000-2002

BVDU Poona College of Pharmacy and Research Centre, Pune

Thesis Title: "Development and Validation of Analytical Method for

Multicomponent Formulation using HPLC"

. Calibrated UV-Visible spectrophotometer and HPLC

. Developed new analytical method for multicomponent formulation using UV-

Visible spectrophotometer and HPLC

. Validated and developed method as per ICH guidelines

. Performed microbial testing

. Prepared test samples and performed analysis of APIs and finished

products samples in accordance with SOPs and GMP requirements

. Performed analysis on automated laboratory instruments such as pH meter,

polarimeter, refractometer, UV-Visible spectrophotometer, TLC, HPLC, Karl

Fisher titration unit and dissolution test apparatus

. Completed calibration of laboratory equipment as per technical manuals

(TM) and SOPs

. Documented and reported results as per established SOPs following GMP and

GDP guidelines

Lecturer Pharmaceutical Analysis 1999-2000

SGS College of Pharmacy, Pune

. Calibrated UV-Visible spectrophotometer and HPLC

. Delivered lectures and conducted practical in Pharmaceutical Analysis

. Conduced Exams for Pharmaceutical Analysis

. Evaluated answer papers as a subject matter expert for theory and

practical examinations

. Participated in various extracurricular activities related to educational

skill set improvements

Dipa Panzade 641-***-****

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EDUCATION

Master of Pharmacy (Quality Assurance) 2000-2002

Bharati Vidyapeeth Deemed University

Bachelor of Pharmacy 1994-1998

University of Pun

PROFESSIONAL TRAINING

Dissolution Testing of Pharmaceuticals

BVDU Poona College of Pharmacy and Research Centre

Inplant Training in Quality Control/ Quality Assurance and Production

(Parenterals, Liquid Orals/ Emulsions/ Packaging)

Rhone-Poulenc

Diploma Course in Office Automation

CDAC-GIST

References available upon request

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