DIPALI PARIKH

**** ****** ***** 224-***-****

Bartlett, IL 60103 nhes12@r.postjobfree.com

Objective:

To find a challenging career opportunity in the areas of Pharmaceuticals, R&D, or Clinical Research.

Summary:

• Experienced Research Associate in the areas of Novel Drug Delivery System, Pharmaceutical Product Development, and Bioavaibility/Bioequivalence Study

• Expertise in conducting a literature review & working Knowledge of Particle Size Analyzer, High Speed Homogenizer, XRD, IR, HPLC

Education:

Master of Science in Pharmacy (Pharmaceutical Technology)

Charotar University of Science and Technology India 2011

*Pending evaluation as waiting for Diploma

Bachelor of Science in Pharmacy

Hemchandracharya North Gujarat University India 2007

Transcript evaluated by World Education Services for Equivalent BS in United States and GPA 3.97/4.00

Thesis:

Formulation and Optimization of Ciprofloxacin HCl loaded Solid Lipid Nanoparticles for Ophthalmic 2010 - 2011

Drug Delivery.

• Ciprofloxacin HCl loaded Solid lipid nanoparticles were developed and optimized for different formulation and process parameters. The developed formulation presented a sustained release effect that provides prolonged drug delivery.

• SLNs were prepared by Double Emulsion (W/O/W) using high speed homogenizer.

Internship:

• Worked as a trainee scientist for sterile manufacturing at Claris Lifescience Limited, India 2010

• Worked as a trainee scientist for tablet, capsule manufacturing at Exotic Laboratories Pvt. Ltd., India 2006

Professional Experience:

Accutest Research Laboratories Pvt. Ltd, India 2008- 2009

Research Associate

• Responsible for procurement, storage and maintenance of accountability of investigational products for bioavaibility/bioequivalence study as per the SOPs and requirement of the different regulatory markets.

• Responsible for dispensing, dosing, reconciliation, and disposal of investigational products of bioavaibility/bioequivalence study as per the SOPs and the requirement of regulatory markets.

• Responsible for writing and designing of basic study protocols, Case report forms (CRFs).

• Responsible for assurance of subject enrollment in the study and retrieval of CRFs

• Assisted in taking Subject Consent and documentation of Informed Consent Forms (ICFs).

• Resolving the queries of internal Quality Assurance audits related to pharmacy department.

• Effectively handled IP related regulatory audits conducted by USFDA and WHO for the pharmacy department

Publication:

D.PARIKH, R.PARIKH Formulation of Ciprofloxacin HCl Loaded Solid Lipid Nanoparticles for Ocular Drug Delivery: Optimization by 22 Factorial Design. Poster has been approved to be presented at 2011 AAPS Annual Meeting and Exposition at Washington DC.

Skills:

MS Windows, MS Office Suite (Excel, PowerPoint, Visio, Access, Word), End Note

References:

References will be available upon request.

*Open to Relocate

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