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Analytical Scientist Resume Example

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JC
Jessica Claire
Montgomery Street, San Francisco, CA 94105 (555) 432-1000, resumesample@example.com
Professional Summary
Procure a position in pharmaceutical Industry and to contribute my knowledge for the growth of the company while I acquire the knowledge to excel in the field of analytical method development.
Skills
  • HPLC (Waters 2690/95-Empower pro), UPLC (Waters Acquity / Acquity console- Empower), GC (Agilent-)
  • IVRT-Franz diffusion cells & Enhancer cells
  • UV spectroscopy , Karl-Fischer-Autosampler , pH meter
  • Particle size analyzer (Malvern)
  • Type I-II dissolution apparatus, XRD, FTIR
  • Good Documentation skills in managing, gathering and reporting test data using statistical tools, ICH Q8
  • Proficient in Microsoft Office (MS Word, Excel, PowerPoint & Outlook)
  • Time management, Communication and Organizational skills, Active member of team and ability to accept and learn from criticism.
Work History
07/2016 to Current Analytical scientist Entegris, Inc. | Logan, ,

Working on preformulation of topical and ophthalmic drug product using
- UHPLC, HPLC, GC, KF,  FTIR. Conduct IVRT testing using Franz diffusion cells and enhancer cells, Method development for Assay,Impurity profiles and residual solvents, Method validation of the In-house developed methods and verification of USP compendial methods. Conduct stability testing activities in the R&D laboratory for new products. Work with the team to develop and validate analytical test methods.  Interpret and communicate analytical results. Work on protocol and report writing. Present progress plan report to management emphasizing open documents and nonconformance. Maintain full compliance with all applicable cGMP regulations and internal SOPs. Contribute towards optimizing laboratory operations to increase efficiency and GMP compliance. Calibrate in-process testing equipment, interpret and analyze experimental data, identified the steps to be taken. Contribute significantly in Over all project by reading guidelines and scientific literature. Create and Maintain Laboratory documentation (notebooks and computer-based), document exact steps followed during analysis execution, calculate and report results in a timely manner. Actively participate in investigation of laboratory results, when required.


01/2016 to 06/2016 Analytical scientist Entegris, Inc. | Round Rock, ,

Working on Analysis of oral drug & topical product using
- HPLC, UV, KF, Dissolution apparatus I & II. Conduct Rheological characterization topical and oral products using Brookfield Viscometer, Densimeter. Conduct Method development for Assay,Impurity profiles and Dissolution for Oral solid dosage forms. Method validation of the In-house developed methods and verification of USP compendial methods. Conduct stability testing activities in the R&D laboratory for new products. Work with the team to develop and validate analytical test methods. Interpret and communicate analytical results. Maintain full compliance with all applicable cGMP regulations and internal SOPs. Contribute towards optimizing laboratory operations to increase efficiency and GMP compliance. Calibrate in-process testing equipment, interpret and analyze experimental data, identified the steps to be taken. Contribute significantly in Overall project by reading guidelines and scientific literature. Create and Maintain Laboratory documentation (notebooks and computer-based), document exact steps followed during analysis execution, calculate and report results in a timely manner.

02/2015 to 09/2015 R&D Biochemist Hemispherex Biopharma | City, ,

Involved in the clinical development of a new a double stranded RNA entity, Ampligen, for its potential treatment viral and immune-based disorders including Chronic Fatigue Syndrome (CFS). Studies involve isolation of the natural killer (NK) cells from the CFS patients from over 20 U.S. clinical trial sites to understand and study its cytotoxic effect on host (K562) cells. Involved in isolation of human peripheral blood mononuclear cells (PBMCs) from whole blood. Performing Cytotoxicity assay, Degranulation assay and Phenotyping assay using Flow Cytometer. Performing Chromium Release assay and quantifying using Liquid Scintillation analyzer. Performing HPLC for determining the purity of polymer end products in the QC. Performing UV-visible spectroscopy for determining purity of product in the QC. Performing SDS-PAGE Electrophoresis & Western Blotting to detect impurities in final product as well as in intermediates. Perform q-PCR to find purity of the final product. Perform ELISA to determine the concentration of the final product. Perform Bioburden testing and total viable count study. Performing all the work tasks with cGMP. K562 (mammalian cell line) and PKH 26 cell line maintenance, Buffer Preparation, Media Preparation. Calibrated and maintained laboratory equipment such as pH meters, Weighing balances and pipettes. Executed appropriate protocol and maintain laboratory record and notebook. Document Review and author SOP.


Education
Expected in 2015 Master of Science | Pharmaceutical sciences Long Island University, Brooklyn , GPA:
Expected in 2011 Bachelor of Science | Pharmacy Mumbai university, Thane , GPA:

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Resume Strength

  • Length
  • Personalization
  • Target Job

Resume Overview

School Attended
  • Long Island University
  • Mumbai university
Job Titles Held:
  • Analytical scientist
  • Analytical scientist
  • R&D Biochemist
Degrees
  • Master of Science
  • Bachelor of Science

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