To obtain a position within a company that allows me to utilize my skills and experience in challenging environment and that will enhance my skills and experience, and that allow me to serve to the best.

Analytical scientist at JStar-Research Inc Cranbury NJ (NOV 2019-Present)

Conduct analytical method development and validation under supervision.

Conduct release testing for GMP raw materials, intermediates and final APIs.

Conduct testing for stability studies and cleaning verification.

Review test data to ensure completion and accuracy.

Write raw material test procedures as needed.

Troubleshoot and maintain analytical instruments. Ensure that instrument calibration and qualification intervals are current.

Write instrument operating, maintenance, and qualification/calibration procedures as needed.

Participate in OOS and deviation investigations, as needed.

Support Quality Assurance as needed during internal audits and audits by clients and regulatory agencies. Assist in the development and implementation of corrective actions related to QC/AD.

QC Chemist-I at Aurolife Pharma, NJ.( JUNE 2017-OCT 2019)

Maintain Quality control Testing Record after finished all tests of finished product.

Analysis Related compound, Assay, CU and Dissolution of finished product and LODs.

Used latest Distek dissolution instruments for tablets and capsules.

Using Empower 3 software for High performance liquid chromatography and gas chromatography.

Analysis from the analytical equipment such as HPLC, UV spectrometer and Dissolution Test

Review and approve the quality system documents to determine compliance with regulatory affairs and standard.

Using Caliber LIMS for filled up all Quality control Testing records.

QC Chemist-I at West-ward pharmaceuticals, Eatontown, NJ, USA.( August 2015-June 2017)

Analysis from the analytical equipment such as HPLC, UV spectrometer and Dissolution Test

Review and approve the quality system documents to determine compliance with regulatory affairs and standard.

Used LIMS Phase I for filled up all Quality control Testing records.

Using Empower 3 software for High performance liquid chromatography and gas chromatography.

Maintain Quality control Testing Record after finished all tests of finished product.

Analysis Related compound, Assay, CU and Dissolution of finished product and LODs.

Used latest Distek dissolution instruments for tablets and capsules.

Analysis finished products Identification on FTIR and Appearance, odor test for tablets and capsules.

Maintain laboratory instrumentations, logbooks, test results and notebooks comply with GMP and SOP as they related to QC laboratories.

Familiar with software such as Microsoft word, Microsoft Excel and other such as relevant software packages such as Empower and other chromatographic Data and control software.

Analysis of stability and finished products.

Chemist at US Pharma Lab. North Brunswick, NJ, USA. [ Jan 2015 –July 2015]

Analysis from the analytical equipment such as HPLC,UV spectrometer and Dissolution Test

Review and approve the quality system documents to determine compliance with regulatory affairs and standard.

Maintain laboratory instrumentations, logbooks, test results and notebooks complies with GMP and SOP as they related to QC laboratories.

QC Chemist at Lincoln pharmaceutical Ltd. In Khatraj, Gujarat, India.

[July 2011- Feb 2012]

Approve all batches and incoming all finished product and routine analysis of the different samples to classify their physical and chemical identity.

Review and approve the quality system documents to determine compliance with regulatory affairs and standard.

Analysis from the analytical equipment such as FT-IR, HPLC, Dissolution Test and spectrometer

Possess knowledge of cGMPs, regulations and risk management requirements to allow for independent assessment of information in accordance with standard operating procedure.

Maintain all analytical equipment according to SOPs.

Ensure that all work meets applicable QA/QC guidelines.’

Complete all paperwork related to analysis.

Review and update test methods and procedures according to SOPs.

Prepare reports to document findings and recommendation.

Maintain analytical instruments, pH meters, UV-VIS and HPLC. .

Maintain an environment of respect and teamwork with all coworkers.

Post Graduate Diploma at Advance Clinical Research [Dec 2009]

Shivarath center of Excellence in clinical research, Gujarat, India

Bachelor of Pharmacy [Dec 2008]

Rajiv Gandhi University of Health Sciences, Shimoga, India

Certificates & Courses:

Registered pharmacy certificate of Gujarat pharmacy council.

Certificate of clinical pharmacist in Nirma University of institute of pharmacy.

Activities

TRAINING EXPERIENCE:

150 hours in 45 days practical industrial training in various department of Lincoln pharmaceutical Ltd. In Khatraj, Gujarat, India.

Laboratory Skills: TLC, titration and chemical and microbiological assays.

Analytical Equipment: HPLC, TLC, GC, UV, UV/Visible Spectro-photometer, Ultracentrifuge, Dissolution and Disintegration, titration and distillation instruments.

Computer: EDMS (Electronic Document Management System)- M-Files, Statistical Software- Minitab 15 & 16, Microsoft Project & Visio, Microsoft Office 2010, Windows ‘98/2000/XP/Vista Prem/7.

OBJECTIVE

EDUCATION

SKILLS

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