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Document Control Chemistry

Iselin, NJ
November 13, 2018

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Steve Hohil 973-***-**** *

» Profile

Over 20 years of hands on experience with analytical instrumentation and chemistry techniques including instrument calibration, troubleshooting and wet chemistry analysis in the pharmaceutical industry.

» Education

B.S. in Chemistry Rutgers University (New Brunswick, NJ) High-Performance Liquid Chromatography Certification Chromak Research (Somerset, NJ)

» Work Experience

C.R. Holdings (Maplewood, NJ)

Property Management Consultant 2015 - Present

Responsible for overseeing commercial real estate properties and investments.

Establish policies and procedures and executed legal agreements. Administer marketing and advertising

Maintain building systems by contracting renovations and maintenance. Prioritize and schedule projects, budgets, and personnel

Eli Lilly Corporation (Branchburg, NJ)

Senior Analytical Chemist 2006 - 2015

Along with a team of scientists, managed laboratory instrumentation and incoming raw material samples. Trained new employees in various wet chemistry and analytical instruments. Responsible for drafting and presenting reports to senior management.

Performed investigations in support of OOS and atypical test results; refine processes accordingly

Extensive knowledge and application of GMP, USP, EP, JP and CFR requirements and regulations

Performed routine and non-routine analysis of raw materials and utilities against specification criteria

Ensured that sampling, testing, and documentation of incoming materials was performed in compliance with established, approved written procedures Sandoz Pharmaceuticals (Dayton, NJ)

Senior QC Chemist 2001 – 2006

Tasked with executing creative solutions for technical transfers of ANDA’s, reviewing batch records and setting specifications for compendia and non-compendia raw materials. Responsible for routine testing as well as method development.

Supervised QC Chemists, Samplers and Technicians and worked with QC Director to ensure release of Raw Materials on schedule

Assisted pharmaceutical development team with reviewing all batch records and testing compliance for technical transfers

Maintained chain of custody for Incoming Test Samples and Incoming Retain Samples

Reviewed and revised SOP’s and Raw Material Specifications as needed

Maintained a cGMP compliant laboratory, responsible for controlling and documenting equipment, reagents, standards and notebooks

Helped Document Control department with reviewing and updating all technical documents American Home Products Corporation (Princeton, NJ) Research Chemist 1993 – 2001

As a member of the analytical chemistry group I tested incoming organically synthesized compounds for identification and impurity.

Analyzed and characterized organically synthesized molecules

Worked as an analytical chemist to support the organic chemists using all instrumental methods of analysis and wet chemistry techniques.

Performed Melting Point, Karl Fisher, Conductivity, TGA, DSC

Analyze samples using Gas Chromatography, NMR, Thin Layer Chromatography, pH meter, UV/Visible Spectroscopy, FTIR

» About

Expertise is all aspects of pharmaceutical testing including raw material and finished products release. HPLC, Dissolution, Total Organic Content Analysis, Carbon, Hydrogen, Nitrogen and Sulfur analysis, Gas Chromatography, NMR, Thin Layer Chromatography, pH meter, UV/Visible Spectroscopy, FTIR, Raman Spectroscopy, Atomic Absorption, Viscometer, Laser Scattering Particle Size analysis, Melting Point, Karl Fisher, Conductivity, TGA, DSC, Bulk and Tapped Density, Particle Sieve Analysis. Fluent in Ukrainian.

Expert drummer for 33 years.

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