Resume - Pharmacy graduate from Mumbai university having about 4 years of work experience...

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Resume #45130

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SUMMARY
- Pharmacy graduate with about 4 years of experience in Pharmaceutical Research and development.

- Extensive work experience in analytical method development, Method Validation and in ANDA (Abbreviated new drug application)

- Advanced skills and knowledge in handling as well as calibration of sophisticated instruments such as HPLC, GC.

Well versed with analytical instruments such as
* HPLC
* GC
* UV Spectrophotometer
* FTIR
* KF Autotitrator
* Dissolution Test Apparatus
* Polarimeter
* Particle Size Analyzer

- Computer knowledge: Well versed with MS-Office, Excel, and Power Point. Good working Knowledge of Internet.
- Individually handled ANDA project till submission to US FDA (Analytical part)
- Analytical method transfer from R & D to manufacturing site.
- Familiar with ICH & GLP Guidelines

PROFESSIONAL EXPERIENCE:
(Present job)
Nicholas Piramal Research Center, Mumbai, India
From March 2005
Designation: Research Associate
Department: Pharmaceutical Research and development (ANDA)

Job Profile:
- Analytical method development with optimization of method for ANDA projects especially of Conventional dosage forms e.g tablets.
- Analytical method validation of assay, dissolution and related substances method.
- Calibration of instruments such as HPLC, Dissolution test apparatus, UV Spectrophotometer etc.
- Preparation of Technical transfer document for ANDA which includes preparation of specifications, standard analytical procedures for pharmaceutical excipients as well as finished product.
- Drug Master Formula review for active pharmacetical ingredients.
- Analysis of a developmental inprocess batches as well as stability samples.

R & D Center Themis Laboratories Pvt. Limited, Mumbai
From June 2003 to March 2004
Designation: Research & Development Officer.
DepartmenT: Pharmaceutical Research and development

Job Profile:
- Analytical method development with optimization of method for sustained released dosage forms, delayed release dosage forms, immediate release dosage forms of Tablet & Pellets (ready for filling in capsules), mouth dissolving tablets & taste masked formulations.
- Analytical method validation for assay, dissolution, and related substances method for sustained released dosage forms and various combinations of drugs eg: Bilayered tablets, immediate release pellets with enteric coated or sustained release pellets for filling in capsules.
- Preparation of Standard operating procedures for quality control & various instruments such as HPLC, Dissolution test apparatus, UV Spectrophotometer etc.
- Preparation of method validation & stability protocols.
- Analysis of in-process as well as stability samples.

Pharmasolve Specialities Pvt. Limited c/o Cipla Limited, Mumbai
From June 2002 to May 2003
Designation: Quality control analyst.
Department: Quality control Department

Job profile:
- Raw materials analysis as well as finished products analysis as per standard test procedures. Finished products include tablets, capsules, liquid orals, lozenges, eye drops, ointments, Creams etc.
- Performance qualification of instruments such as HPLC, Dissolution test apparatus.
- HPLC column maintainence as well as regeneration of columns.
- Reference Standards & Working Standards Management

EDUCATION:
- Bachelors Degree in Pharmacy
The Bombay College Of Pharmacy, Mumbai, India in 2002

- Diploma in Pharmacy
Principal K. M. Kundanani Pharmacy Polytechnic, Mumbai, India in 1997

- Computer knowledge: Well versed with MS-Office, Excel, Power Point. Good working Knowledge of Internet

* PROFESSIONAL ASPIRATION:
To be associated with a research oriented quality conscious
Organization and achieve reputation and growth in the profession by attainment of organizational goals through innovation, hardwork and teamwork.

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