Technical Writer Resume

Objective: A position as a Chemist.

Professional Profile:
Hands on experience with the following instruments:
HPLC, UPLC, GC, Dissolution, UV-Vis, Atomic Absorption Spectroscopy, FT-IR, KF moisture analyzer and other laboratory instruments.
Training: Trained on writing and updating SOP, method development, method validation and instrument trouble shooting and calibration (GC and HPLC).
Software used: Empower, Millennium 3.2, Perkin Elmer UV Win Lab for UV-Vis, HP Chem. Station, AA Win lab, and Citrix..

Experience:
Confidential, Allendale, NJ
Technical Writer 4/2011-12/2011

Writing technical reports to support all assay validation and method transfer studies.
Creates all routine analytical reports from the Analytical group.
Responsible for extracting the necessary details from the spread sheet and creating final reports/table

Confidential, Pomona NY 10970
A R D Chemist II 7/2005 - 12/2010

Develop and validate analytical test method.
Perform non-routine chemical analyses; analyze and draw conclusions.
Interprets test data and write reports.
Recommends needed equipment and technologies to perform relevant analyses to meet project needs.
Analyzed raw materials, finished products and stability samples for compliance with specifications and standards.
Used HPLC, UPLC, UV Vis., GC and dissolution apparatus for all analysis.
Developed assay, impurity, and dissolution for finished products by using HPLC, UPLC, GC and UV – Vis spectrophotometer.
Verify methods for finished products including specification, linearity, method precision, robustness, and forced degradation.
Support product formulation department by providing assay, impurity and dissolution profile for initial and stability samples.
Did a comparative evaluation of in house developmental product form reference listing drug (brand drug) for product development.
Performs method development, method validation, stability, and method transfer and QA release samples.
Conducts basic instrument troubleshooting.
Conducts data analysis and identify trends.
Updates method validation protocols and SOP.
Communicates across department functions to keep projects on schedule, taking broader responsibility for project completion.

Confidential, Union, NJ 07083
Quality Control Chemist II 6/2003 - 7/2005

Analyses done were FP assay, impurities and degradation, foreign particulate, moisture, dose uniformity, content uniformity and dissolution profile.
Review analytical data and documentation, reports laboratory deviations and performs laboratory investigations.
Interprets test data and writes reports.
Review and updates SOP’s.
Trained and performed instrument calibrations (HPLC and GC).

Confidential, Leonia, NJ 07605
QC Chemist 3/2002 - 3/2003

Responsible for analysis of multi vitamins, finished products and raw materials using GC, HPLC, AA, UV, FT-IR, TLC and wet chemistry.
Performed method validation, process validation and method development.
Reviewed analytical data and checked laboratory notebooks.

Confidential, Mahwah NJ 07430
QC Chemist 10/2000 - 3/2002

Responsible for in- process, raw materials and finished products using GC, HPLC, wet chemistry, physical testing and distillation.
Performed sensory test as to taste, color and odor of in process and finished products and raw materials.

Confidential, Maywood, NJ 07607
QC Chemist 12/1997 - 6/1999

Did a wide variety of testing of chemical intermediates. These tests include Fatty Acid Esters, Alcohol Esters, Synthetic Lubricants and Surfactants using GC, FT-IR, HPLC, Karl Fisher and wet chemistry.
Review analytical data and laboratory notebooks. Reviewed and updated SOPs and product specifications.
Calibration of laboratory instruments such as GC, pH meter and Karl Fisher.

Education:
M.S. in Chemistry
B.S. in Chemical Engineering

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